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Sample records for hydrocarbon gravimetric method

  1. New gravimetric method for cobalt.

    PubMed

    Chatterjee, G P; Ray, H N; Biswas, K

    1966-10-01

    A new gravimetric method for the determination of cobalt is described, based on precipitation from acidic solution with a reagent prepared by heating alpha-nitroso-beta-naphthol in a mixture of glacial acetic acid, hydrogen peroxide and syrupy phosphoric acid. The cobalt is weighed, after ignition of the precipitate, as Co(3)O(4). Iron(III), copper, chromium(III), vanadium(V), tungsten(VI), aluminium, molybdenum, nickel, titanium, zirconium, uranium(VI) and cerium do not interfere. PMID:18960030

  2. Gravimetric method for the determination of diclofenac in pharmaceutical preparations.

    PubMed

    Tubino, Matthieu; De Souza, Rafael L

    2005-01-01

    A gravimetric method for the determination of diclofenac in pharmaceutical preparations was developed. Diclofenac is precipitated from aqueous solution with copper(II) acetate in pH 5.3 (acetic acid/acetate buffer). Sample aliquots had approximately the same quantity of the drug content in tablets (50 mg) or in ampules (75 mg). The observed standard deviation was about +/- 2 mg; therefore, the relative standard deviation (RSD) was approximately 4% for tablet and 3% for ampule preparations. The results were compared with those obtained with the liquid chromatography method recommended in the United States Pharmacopoeia using the statistical Student's t-test. Complete agreement was observed. It is possible to obtain more precise results using higher aliquots, for example 200 mg, in which case the RSD falls to 1%. This gravimetric method, contrary to what is expected for this kind of procedure, is relatively fast and simple to perform. The main advantage is the absolute character of the gravimetric analysis.

  3. Gravimetric method for in vitro calibration of skin hydration measurements.

    PubMed

    Martinsen, Ørjan G; Grimnes, Sverre; Nilsen, Jon K; Tronstad, Christian; Jang, Wooyoung; Kim, Hongsig; Shin, Kunsoo; Naderi, Majid; Thielmann, Frank

    2008-02-01

    A novel method for in vitro calibration of skin hydration measurements is presented. The method combines gravimetric and electrical measurements and reveals an exponential dependency of measured electrical susceptance to absolute water content in the epidermal stratum corneum. The results also show that absorption of water into the stratum corneum exhibits three different phases with significant differences in absorption time constant. These phases probably correspond to bound, loosely bound, and bulk water.

  4. Global gravimetric geoid model based a new method

    NASA Astrophysics Data System (ADS)

    Shen, W. B.; Han, J. C.

    2012-04-01

    The geoid, defined as the equipotential surface nearest to the mean sea level, plays a key role in physical geodesy and unification of height datum system. In this study, we introduce a new method, which is quite different from the conventional geoid modeling methods (e.g., Stokes method, Molodensky method), to determine the global gravimetric geoid (GGG). Based on the new method, using the dada base of the external Earth gravity field model EGM2008, digital topographic model DTM2006.0 and crust density distribution model CRUST2.0, we first determined the inner geopotential field until to the depth of D, and then established a GGG model , the accuracy of which is evaluated by comparing with the observations from USA, AUS, some parts of Canada, and some parts of China. The main idea of the new method is stated as follows. Given the geopotential field (e.g. EGM2008) outside the Earth, we may determine the inner geopotential field until to the depth of D by using Newtonian integral, once the density distribution model (e.g. CRUST2.0) of a shallow layer until to the depth D is given. Then, based on the definition of the geoid (i.e. an equipotential surface nearest to the mean sea level) one may determine the GGG. This study is supported by Natural Science Foundation China (grant No.40974015; No.41174011; No.41021061; No.41128003).

  5. A comparison of four gravimetric fine particle sampling methods.

    PubMed

    Yanosky, J D; MacIntosh, D L

    2001-06-01

    A study was conducted to compare four gravimetric methods of measuring fine particle (PM2.5) concentrations in air: the BGI, Inc. PQ200 Federal Reference Method PM2.5 (FRM) sampler; the Harvard-Marple Impactor (HI); the BGI, Inc. GK2.05 KTL Respirable/Thoracic Cyclone (KTL); and the AirMetrics MiniVol (MiniVol). Pairs of FRM, HI, and KTL samplers and one MiniVol sampler were collocated and 24-hr integrated PM2.5 samples were collected on 21 days from January 6 through April 9, 2000. The mean and standard deviation of PM2.5 levels from the FRM samplers were 13.6 and 6.8 microg/m3, respectively. Significant systematic bias was found between mean concentrations from the FRM and the MiniVol (1.14 microg/m3, p = 0.0007), the HI and the MiniVol (0.85 microg/m3, p = 0.0048), and the KTL and the MiniVol (1.23 microg/m3, p = 0.0078) according to paired t test analyses. Linear regression on all pairwise combinations of the sampler types was used to evaluate measurements made by the samplers. None of the regression intercepts was significantly different from 0, and only two of the regression slopes were significantly different from 1, that for the FRM and the MiniVol [beta1 = 0.91, 95% CI (0.83-0.99)] and that for the KTL and the MiniVol [beta1 = 0.88, 95% CI (0.78-0.98)]. Regression R2 terms were 0.96 or greater between all pairs of samplers, and regression root mean square error terms (RMSE) were 1.65 microg/m3 or less. These results suggest that the MiniVol will underestimate measurements made by the FRM, the HI, and the KTL by an amount proportional to PM2.5 concentration. Nonetheless, these results indicate that all of the sampler types are comparable if approximately 10% variation on the mean levels and on individual measurement levels is considered acceptable and the actual concentration is within the range of this study (5-35 microg/m3).

  6. Comparison of fine particle measurements from a direct-reading instrument and a gravimetric sampling method.

    PubMed

    Kim, Jee Young; Magari, Shannon R; Herrick, Robert F; Smith, Thomas J; Christiani, David C

    2004-11-01

    Particulate air pollution, specifically the fine particle fraction (PM2.5), has been associated with increased cardiopulmonary morbidity and mortality in general population studies. Occupational exposure to fine particulate matter can exceed ambient levels by a large factor. Due to increased interest in the health effects of particulate matter, many particle sampling methods have been developed In this study, two such measurement methods were used simultaneously and compared. PM2.5 was sampled using a filter-based gravimetric sampling method and a direct-reading instrument, the TSI Inc. model 8520 DUSTTRAK aerosol monitor. Both sampling methods were used to determine the PM2.5 exposure in a group of boilermakers exposed to welding fumes and residual fuel oil ash. The geometric mean PM2.5 concentration was 0.30 mg/m3 (GSD 3.25) and 0.31 mg/m3 (GSD 2.90)from the DUSTTRAK and gravimetric method, respectively. The Spearman rank correlation coefficient for the gravimetric and DUSTTRAK PM2.5 concentrations was 0.68. Linear regression models indicated that log, DUSTTRAK PM2.5 concentrations significantly predicted loge gravimetric PM2.5 concentrations (p < 0.01). The association between log(e) DUSTTRAK and log, gravimetric PM2.5 concentrations was found to be modified by surrogate measures for seasonal variation and type of aerosol. PM2.5 measurements from the DUSTTRAK are well correlated and highly predictive of measurements from the gravimetric sampling method for the aerosols in these work environments. However, results from this study suggest that aerosol particle characteristics may affect the relationship between the gravimetric and DUSTTRAK PM2.5 measurements. Recalibration of the DUSTTRAK for the specific aerosol, as recommended by the manufacturer, may be necessary to produce valid measures of airborne particulate matter.

  7. Gravimetric methods for the preparation of standard gas mixtures

    NASA Astrophysics Data System (ADS)

    Milton, M. J. T.; Vargha, G. M.; Brown, A. S.

    2011-10-01

    The most widely used method for the preparation of primary standard gas mixtures involves weighing the individual components into a cylinder. We present a new mathematical description of the method and its uncertainties. We use this to demonstrate how strategies for serial dilution can be identified that minimize the uncertainty in the final mixture and show how they can be implemented practically. We review published reports of high accuracy gravimetry and give examples of relative uncertainties in the composition of standards approaching 1 part-per-million in the best cases and in the range of 100 to 1000 parts-per-million more typically.

  8. The gravimetric method for the determination of residual moisture in freeze-dried biological products.

    PubMed

    May, J C; Wheeler, R M; Grim, E

    1989-06-01

    The gravimetric test for the determination of residual moisture in freeze-dried biological products performed in a humidity- and temperature-controlled room with the use of scrupulous gravimetric analytical technique can be used to accurately determine residual moisture in freeze-dried biological products such as antihemophilic factor (human) or honey bee venom allergenic extract. This method determines the first water of hydration of sodium tartrate dihydrate (7.93%) to within 1.3% of the calculated value with a relative standard deviation of 0.3% for 10 replicates. For this gravimetric procedure, freeze-dried samples containing from 1.12 to 4.4% residual moisture had relative standard deviations ranging from 3.6 to 9.1%. Samples containing less than 1.0% residual moisture by the gravimetric method such as intravenous immune globulin and antihemophilic factor (human) had relative standard deviations ranging from 16.7 to 47.0%. Relative standard deviations for residual moisture tests performed on comparable samples by the Karl Fischer and thermogravimetric methods showed similar variability. PMID:2743789

  9. Comparison of macro-gravimetric and micro-colorimetric lipid determination methods.

    PubMed

    Inouye, Laura S; Lotufo, Guiherme R

    2006-10-15

    In order to validate a method for lipid analysis of small tissue samples, the standard macro-gravimetric method of Bligh-Dyer (1959) [E.G. Bligh, W.J. Dyer, Can. J. Biochem. Physiol. 37 (1959) 911] and a modification of the micro-colorimetric assay developed by Van Handel (1985) [E. Van Handel, J. Am. Mosq. Control Assoc. 1 (1985) 302] were compared. No significant differences were observed for wet tissues of two species of fish. However, limited analysis of wet tissue of the amphipod, Leptocheirusplumulosus, indicated that the Bligh-Dyer gravimetric method generated higher lipid values, most likely due to the inclusion of non-lipid materials. Additionally, significant differences between the methods were observed with dry tissues, with the micro-colorimetric method consistently reporting calculated lipid values greater than as reported by the gravimetric method. This was most likely due to poor extraction of dry tissue in the standard Bligh-Dyer method, as no significant differences were found when analyzing a single composite extract. The data presented supports the conclusion that the micro-colorimetric method described in this paper is accurate, rapid, and minimizes time and solvent use.

  10. Measuring intestinal fluid transport in vitro: Gravimetric method versus non-absorbable marker.

    PubMed

    Whittamore, Jonathan M; Genz, Janet; Grosell, Martin; Wilson, Rod W

    2016-04-01

    The gut sac is a long-standing, widely used in vitro preparation for studying solute and water transport, and calculation of these fluxes requires an accurate assessment of volume. This is commonly determined gravimetrically by measuring the change in mass over time. While convenient this likely under-estimates actual net water flux (Jv) due to tissue edema. We evaluated whether the popular in vivo volume marker [(14)C]-PEG 4000, offers a more representative measure of Jvin vitro. We directly compared these two methods in five teleost species (toadfish, flounder, rainbow trout, killifish and tilapia). Net fluid absorption by the toadfish intestine based on PEG was significantly higher, by almost 4-fold, compared to gravimetric measurements, compatible with the latter under-estimating Jv. Despite this, PEG proved inconsistent for all of the other species frequently resulting in calculation of net secretion, in contrast to absorption seen gravimetrically. Such poor parallelism could not be explained by the absorption of [(14)C]-PEG (typically <1%). We identified a number of factors impacting the effectiveness of PEG. One was adsorption to the surface of sample tubes. While it was possible to circumvent this using unlabelled PEG 4000, this had a deleterious effect on PEG-based Jv. We also found sequestration of PEG within the intestinal mucus. In conclusion, the short-comings associated with the accurate representation of Jv by gut sac preparations are not overcome by [(14)C]-PEG. The gravimetric method therefore remains the most reliable measure of Jv and we urge caution in the use of PEG as a volume marker. PMID:26794612

  11. Evaluation of gravimetric methods for dissoluble matter in extracts of environmental samples

    SciTech Connect

    Lafleur, A.L.; Monchamp, P.A.; Plummer, E.F.; Kruzel, E.L.

    1986-01-01

    A number of gravimetric methods were evaluated for the determination of dissolved matter in solvent extracts of combustion samples. The methods described included thermogravimetric analysis, weighing after evaporation under nitrogen, and a microscale evaporation method developed in this study. A well characterized combustion sample, known to consist primarily of alkylated bicyclic and tricyclic aromatic compounds, served as a reference material. Results for the three methods are presented and compared. Although the thermogravimetric analyzer was found to be accurate and versatile, a good compromise between cost, time and accuracy was provided by the microscale evaporation method.

  12. A highly accurate method for determination of dissolved oxygen: gravimetric Winkler method.

    PubMed

    Helm, Irja; Jalukse, Lauri; Leito, Ivo

    2012-09-01

    A high-accuracy Winkler titration method has been developed for determination of dissolved oxygen concentration. Careful analysis of uncertainty sources relevant to the Winkler method was carried out and the method was optimized for minimizing all uncertainty sources as far as practical. The most important improvements were: gravimetric measurement of all solutions, pre-titration to minimize the effect of iodine volatilization, accurate amperometric end point detection and careful accounting for dissolved oxygen in the reagents. As a result, the developed method is possibly the most accurate method of determination of dissolved oxygen available. Depending on measurement conditions and on the dissolved oxygen concentration the combined standard uncertainties of the method are in the range of 0.012-0.018 mg dm(-3) corresponding to the k=2 expanded uncertainty in the range of 0.023-0.035 mg dm(-3) (0.27-0.38%, relative). This development enables more accurate calibration of electrochemical and optical dissolved oxygen sensors for routine analysis than has been possible before.

  13. [Determination of total, soluble and insoluble dietary fiber in foods by enzymatic-gravimetric method].

    PubMed

    Yang, X; Yang, Y; Zhou, R; Bian, L

    2001-11-01

    For studying the contents of dietary fiber in general foods and functional foods, a enzymatic-gravimetric method recommended by AOAC was established in our laboratory. The method for the determination of total, soluble and insoluble dietary fiber in foods and functional foods could be used for many other kind of foods. The relative standard deviations (RSD) of reproducibility between-run and within-run were 2.04%-7.85%, 3.42%-55.23% respectively. The repeatability of the methods was good, and the methods are suitable for many foods.

  14. Gravimetric water distribution assessment from geoelectrical methods (ERT and EMI) in municipal solid waste landfill.

    PubMed

    Dumont, Gaël; Pilawski, Tamara; Dzaomuho-Lenieregue, Phidias; Hiligsmann, Serge; Delvigne, Frank; Thonart, Philippe; Robert, Tanguy; Nguyen, Frédéric; Hermans, Thomas

    2016-09-01

    The gravimetric water content of the waste material is a key parameter in waste biodegradation. Previous studies suggest a correlation between changes in water content and modification of electrical resistivity. This study, based on field work in Mont-Saint-Guibert landfill (Belgium), aimed, on one hand, at characterizing the relationship between gravimetric water content and electrical resistivity and on the other hand, at assessing geoelectrical methods as tools to characterize the gravimetric water distribution in a landfill. Using excavated waste samples obtained after drilling, we investigated the influences of the temperature, the liquid phase conductivity, the compaction and the water content on the electrical resistivity. Our results demonstrate that Archie's law and Campbell's law accurately describe these relationships in municipal solid waste (MSW). Next, we conducted a geophysical survey in situ using two techniques: borehole electromagnetics (EM) and electrical resistivity tomography (ERT). First, in order to validate the use of EM, EM values obtained in situ were compared to electrical resistivity of excavated waste samples from corresponding depths. The petrophysical laws were used to account for the change of environmental parameters (temperature and compaction). A rather good correlation was obtained between direct measurement on waste samples and borehole electromagnetic data. Second, ERT and EM were used to acquire a spatial distribution of the electrical resistivity. Then, using the petrophysical laws, this information was used to estimate the water content distribution. In summary, our results demonstrate that geoelectrical methods represent a pertinent approach to characterize spatial distribution of water content in municipal landfills when properly interpreted using ground truth data. These methods might therefore prove to be valuable tools in waste biodegradation optimization projects. PMID:26926783

  15. Gravimetric water distribution assessment from geoelectrical methods (ERT and EMI) in municipal solid waste landfill.

    PubMed

    Dumont, Gaël; Pilawski, Tamara; Dzaomuho-Lenieregue, Phidias; Hiligsmann, Serge; Delvigne, Frank; Thonart, Philippe; Robert, Tanguy; Nguyen, Frédéric; Hermans, Thomas

    2016-09-01

    The gravimetric water content of the waste material is a key parameter in waste biodegradation. Previous studies suggest a correlation between changes in water content and modification of electrical resistivity. This study, based on field work in Mont-Saint-Guibert landfill (Belgium), aimed, on one hand, at characterizing the relationship between gravimetric water content and electrical resistivity and on the other hand, at assessing geoelectrical methods as tools to characterize the gravimetric water distribution in a landfill. Using excavated waste samples obtained after drilling, we investigated the influences of the temperature, the liquid phase conductivity, the compaction and the water content on the electrical resistivity. Our results demonstrate that Archie's law and Campbell's law accurately describe these relationships in municipal solid waste (MSW). Next, we conducted a geophysical survey in situ using two techniques: borehole electromagnetics (EM) and electrical resistivity tomography (ERT). First, in order to validate the use of EM, EM values obtained in situ were compared to electrical resistivity of excavated waste samples from corresponding depths. The petrophysical laws were used to account for the change of environmental parameters (temperature and compaction). A rather good correlation was obtained between direct measurement on waste samples and borehole electromagnetic data. Second, ERT and EM were used to acquire a spatial distribution of the electrical resistivity. Then, using the petrophysical laws, this information was used to estimate the water content distribution. In summary, our results demonstrate that geoelectrical methods represent a pertinent approach to characterize spatial distribution of water content in municipal landfills when properly interpreted using ground truth data. These methods might therefore prove to be valuable tools in waste biodegradation optimization projects.

  16. Photometrically measured continuous personal PM(2.5) exposure: levels and correlation to a gravimetric method.

    PubMed

    Lanki, Timo; Alm, Sari; Ruuskanen, Juhani; Janssen, Nicole A H; Jantunen, Matti; Pekkanen, Juha

    2002-05-01

    There is evidence that hourly variations in exposure to airborne particulate matter (PM) may be associated with adverse health effects. Still there are only few published data on short-term levels of personal exposure to PM in community settings. The objectives of the study were to assess hourly and shorter-term variations in personal PM(2.5) exposure in Helsinki, Finland, and to compare results from portable photometers to simultaneously measured gravimetric concentrations. The effect of relative humidity on the photometric results was also evaluated. Personal PM(2.5) exposures of elderly persons were assessed for 24 h every second week, resulting in 308 successful measurements from 47 different subjects. Large changes in concentrations in minutes after cooking or changing microenvironment were seen. The median of daily 1-h maxima was over twice the median of 24-h averages. There was a strong significant association between the two means, which was not linear. Median (95th percentile) of the photometric 24-h concentrations was 12.1 (37.7) and of the 24-h gravimetric concentrations 9.2 (21.3) microg/m3. The correlation between the photometric and the gravimetric method was quite good (R2=0.86). Participants spent 94.1% of their time indoors or in a vehicle, where relative humidity is usually low and thus not likely to cause significant effects on photometric results. Even outdoors, the relative humidity had only modest effect on concentrations. Photometers are a promising method to explore the health effects of short-term variation in personal PM(2.5) exposure.

  17. Comparison of gravimetric, creamatocrit and esterified fatty acid methods for determination of total fat content in human milk.

    PubMed

    Du, Jian; Gay, Melvin C L; Lai, Ching Tat; Trengove, Robert D; Hartmann, Peter E; Geddes, Donna T

    2017-02-15

    The gravimetric method is considered the gold standard for measuring the fat content of human milk. However, it is labor intensive and requires large volumes of human milk. Other methods, such as creamatocrit and esterified fatty acid assay (EFA), have also been used widely in fat analysis. However, these methods have not been compared concurrently with the gravimetric method. Comparison of the three methods was conducted with human milk of varying fat content. Correlations between these methods were high (r(2)=0.99). Statistical differences (P<0.001) were observed in the overall fat measurements and within each group (low, medium and high fat milk) using the three methods. Overall, stronger correlation with lower mean (4.73g/L) and percentage differences (5.16%) was observed with the creamatocrit than the EFA method when compared to the gravimetric method. Furthermore, the ease of operation and real-time analysis make the creamatocrit method preferable. PMID:27664665

  18. Comparison of gravimetric, creamatocrit and esterified fatty acid methods for determination of total fat content in human milk.

    PubMed

    Du, Jian; Gay, Melvin C L; Lai, Ching Tat; Trengove, Robert D; Hartmann, Peter E; Geddes, Donna T

    2017-02-15

    The gravimetric method is considered the gold standard for measuring the fat content of human milk. However, it is labor intensive and requires large volumes of human milk. Other methods, such as creamatocrit and esterified fatty acid assay (EFA), have also been used widely in fat analysis. However, these methods have not been compared concurrently with the gravimetric method. Comparison of the three methods was conducted with human milk of varying fat content. Correlations between these methods were high (r(2)=0.99). Statistical differences (P<0.001) were observed in the overall fat measurements and within each group (low, medium and high fat milk) using the three methods. Overall, stronger correlation with lower mean (4.73g/L) and percentage differences (5.16%) was observed with the creamatocrit than the EFA method when compared to the gravimetric method. Furthermore, the ease of operation and real-time analysis make the creamatocrit method preferable.

  19. Gravimetric approach to the standard addition method in instrumental analysis. 1.

    PubMed

    Kelly, W Robert; MacDonald, Bruce S; Guthrie, William F

    2008-08-15

    A mathematical formulation for a gravimetric approach to the univariate standard addition method (SAM) is presented that has general applicability for both liquids and solids. Using gravimetry rather than volumetry reduces the preparation time, increases design flexibility, and makes increased accuracy possible. SAM has most often been used with analytes in aqueous solutions that are aspirated into flames or plasmas and determined by absorption, emission, or mass spectrometric techniques. The formulation presented here shows that the method can also be applied to complex matrixes, such as distillate and residual fuel oils, using techniques such as X-ray fluorescence (XRF) or combustion combined with atomic fluorescence or absorption. These techniques, which can be subject to matrix-induced interferences, could realize the same benefits that have been demonstrated for dilute aqueous solutions.

  20. Method for producing viscous hydrocarbons

    DOEpatents

    Poston, Robert S.

    1982-01-01

    A method for recovering viscous hydrocarbons and synthetic fuels from a subterranean formation by drilling a well bore through the formation and completing the well by cementing a casing means in the upper part of the pay zone. The well is completed as an open hole completion and a superheated thermal vapor stream comprised of steam and combustion gases is injected into the lower part of the pay zone. The combustion gases migrate to the top of the pay zone and form a gas cap which provides formation pressure to produce the viscous hydrocarbons and synthetic fuels.

  1. The Uganda Gravimetric Geoid Model 2014 Computed by The KTH Method

    NASA Astrophysics Data System (ADS)

    Sjöberg, L. E.; Gidudu, A.; Ssengendo, R.

    2015-05-01

    For many developing countries such as Uganda, precise gravimetric geoid determination is hindered by the low quantity and quality of the terrestrial gravity data. With only one gravity data point per 65 km2, gravimetric geoid determination in Uganda appears an impossible task. However, recent advances in geoid modelling techniques coupled with the gravity-field anomalies from the Gravity Field and Steady-State Ocean Circulation Explorer (GOCE) satellite mission have opened new avenues for geoid determination especially for areas with sparse terrestrial gravity. The present study therefore investigates the computation of a gravimetric geoid model overUganda (UGG2014) using the Least Squares Modification of Stokes formula with additive corrections. UGG2014 was derived from sparse terrestrial gravity data from the International Gravimetric Bureau, the 3 arc second SRTM ver4.1 Digital Elevation Model from CGIAR-CSI and the GOCE-only global geopotential model GO_CONS_GCF_2_TIM_R5. To compensate for the missing gravity data in the target area, we used the surface gravity anomalies extracted from the World Gravity Map 2012. Using 10 Global Navigation Satellite System (GNSS)/levelling data points distributed over Uganda, the RMS fit of the gravimetric geoid model before and after a 4-parameter fit is 11 cm and 7 cm respectively. These results show that UGG2014 agrees considerably better with GNSS/levelling than any other recent regional/ global gravimetric geoid model. The results also emphasize the significant contribution of the GOCE satellite mission to the gravity field recovery, especially for areas with very limited terrestrial gravity data.With an RMS of 7 cm, UGG2014 is a significant step forward in the modelling of a "1-cm geoid" over Uganda despite the poor quality and quantity of the terrestrial gravity data used for its computation.

  2. Comparison of gravimetric and gas chromatographic methods for assessing performance of textile materials against liquid pesticide penetration.

    PubMed

    Shaw, Anugrah; Abbi, Ruchika

    2004-01-01

    Penetration of liquid pesticides through textile materials is a criterion for determining the performance of protective clothing used by pesticide handlers. The pipette method is frequently used to apply liquid pesticides onto textile materials to measure penetration. Typically, analytical techniques such as Gas Chromatography (GC) are used to measure percentage penetration. These techniques are labor intensive and costly. A simpler gravimetric method was developed, and tests were conducted to compare the gravimetric and GC methods of analysis. Three types of pesticide formulations and 4 fabrics were used for the study. Diluted pesticide formulations were pipetted onto the test specimens and percentage penetration was measured using the 2 methods. For homogeneous formulation, the results of the two methods were fairly comparable. However, due to the filtering action of the textile materials, there were differences in the percentage penetration between the 2 methods for formulations that were not homogeneous.

  3. A simple, gravimetric method to quantify inorganic carbon in calcareous soils

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Total carbon (TC) in calcareous soils has two components: inorganic carbon (IC) as calcite and or dolomite and organic carbon (OC) in the soil organic matter. The IC must be measured and subtracted from TC to obtain OC. Our objective was to develop a simple gravimetric technique to quantify IC. Th...

  4. Catalytic method for synthesizing hydrocarbons

    DOEpatents

    Sapienza, R.S.; Sansone, M.J.; Slegeir, W.A.R.

    A method for synthesizing hydrocarbons from carbon monoxide and hydrogen by contacting said gases with a slurry of a catalyst composed of palladium or platinum and cobalt supported on a solid phase is disclosed. The catalyst is prepared by heating a heterogeneous component of the palladium or platinum deposited on the solid support in a solution of cobalt carbonyl or precursors thereof. The catalyst exhibits excellent activity, stability in air, and produces highly desirable product fractions even with dilute gaseous reactants.

  5. Catalytic method for synthesizing hydrocarbons

    DOEpatents

    Sapienza, Richard S.; Sansone, Michael J.; Slegeir, William A. R.

    1984-01-01

    A method for synthesizing hydrocarbons from carbon monoxide and hydrogen by contacting said gases with a slurry of a catalyst composed of palladium or platinum and cobalt supported on a solid phase is disclosed. The catalyst is prepared by heating a heterogeneous component of the palladium or platinum deposited on the solid support in a solution of cobalt carbonyl or precursors thereof. The catalyst exhibits excellent activity, stability in air, and produces highly desirable product fractions even with dilute gaseous reactants.

  6. Alternatives to the gravimetric method for quantification of diesel particulate matter near the lower level of detection.

    PubMed

    Swanson, Jacob; Kittelson, David; Pui, David; Watts, Winthrop

    2010-10-01

    This paper is part of the Journal of the Air & Waste Management Association's 2010 special issue on combustion aerosol measurements. The issue is a combination of papers that synthesize and evaluate ideas and perspectives that were presented by experts at a series of workshops sponsored by the Coordinating Research Council that aimed to evaluate the current and future status of diesel particulate matter (DPM) measurement. Measurement of DPM is a complex issue with many stakeholders, including air quality management and enforcement agencies, engine manufacturers, health experts, and climatologists. Adoption of the U.S. Environmental Protection Agency 2007 heavy-duty engine DPM standards posed a unique challenge to engine manufacturers. The new standards reduced DPM emissions to the point that improvements to the gravimetric method were required to increase the accuracy and the sensitivity of the measurement. Despite these improvements, the method still has shortcomings. The objectives of this paper are to review the physical and chemical properties of DPM that make gravimetric measurement difficult at very low concentrations and to review alternative metrics and methods that are potentially more accurate, sensitive, and specific. Particle volatility, size, surface area, and number metrics are considered, as well as methods to quantify them. Although the authors believe that an alternative method is required to meet the needs of engine manufacturers, the methods reviewed in the paper are applicable to other areas where the gravimetric method detection limit is approached and greater accuracy and sensitivity are required. The paper concludes by suggesting a method to measure active surface area, combined with a method to separate semi-volatile and solid fractions to further increase the specificity of the measurement, has potential for reducing the lower detection limit of DPM and enabling engine manufacturers to reduce DPM emissions in the future.

  7. Investigations on vertical crustal movements in the Venezuelan Andes by gravimetric methods

    NASA Technical Reports Server (NTRS)

    Drewes, H.

    1978-01-01

    A precise gravimetric network has been installed in the Venezuelan Andes to study eventual gravity changes due to vertical tectonic movements. The design and the measurements of the network are described and the accuracy is estimated. In the center of the region a local gravity network has been reobserved three times. The detected variations are discussed. In order to obtain a genuine statement as far as possible about the significance of observed gravity changes, requirements for the procedure of monitoring precise gravity networks are pointed out.

  8. The GLOBE Soil Moisture Project's examination of a low-technology method for measuring gravimetric soil moisture

    NASA Astrophysics Data System (ADS)

    Whitaker, M. P. L.; Ferre, T. P. A.; Nijssen, B.; Washburne, J.

    2003-04-01

    GLOBE (see http://www.globe.org) is an NSF-funded effort that supports a worldwide hands-on, primary and secondary school-based science and education program. The GLOBE Soil Moisture Project (see http://www.hwr.arizona.edu/globe/sci/SM/SMC/) is a subset of the overall Program, and aims to mobilize GLOBE-participating students worldwide to collect near-surface (i.e. 0-5 cm and 10 cm below ground surface) gravimetric soil moisture data twice a year. The selected annual target dates are during World Space Week/U.S Earth Science Week (early October) and Earth Day Week (mid-April). In order to include schools with limited resources, the authors are examining the reliability of a low-technology method of measuring soil moisture, namely, the "light-bulb" method of drying soil samples. The device uses the heat from a low-wattage light bulb under an inverted, insulated container under which soil samples are placed to dry. Results from preliminary testing of the light-bulb device will be compared with results from samples dries in a traditional 105 C convection oven. A method will be proposed for using the light bulb device to yield results comparable to those of the standard gravimetric methods that use convection or microwave ovens.

  9. Determination of total dietary fiber (CODEX definition) by enzymatic-gravimetric method and liquid chromatography: collaborative study.

    PubMed

    McCleary, Barry V; DeVries, Jonathan W; Rader, Jeanne I; Cohen, Gerald; Prosky, Leon; Mugford, David C; Champ, Martine; Okuma, Kazuhiro

    2010-01-01

    A method for the determination of total dietary fiber (TDF), as defined by the CODEX Alimentarius, was validated in foods. Based upon the principles of AOAC Official Methods 985.29, 991.43, 2001.03, and 2002.02, the method quantitates high- and low-molecular-weight dietary fiber (HMWDF and LMWDF, respectively). In 2007, McCleary described a method of extended enzymatic digestion at 37 degrees C to simulate human intestinal digestion followed by gravimetric isolation and quantitation of HMWDF and the use of LC to quantitate low-molecular-weight soluble dietary fiber (LMWSDF). The method thus quantitates the complete range of dietary fiber components from resistant starch (by utilizing the digestion conditions of AOAC Method 2002.02) to digestion resistant oligosaccharides (by incorporating the deionization and LC procedures of AOAC Method 2001.03). The method was evaluated through an AOAC collaborative study. Eighteen laboratories participated with 16 laboratories returning valid assay data for 16 test portions (eight blind duplicates) consisting of samples with a range of traditional dietary fiber, resistant starch, and nondigestible oligosaccharides. The dietary fiber content of the eight test pairs ranged from 11.57 to 47.83%. Digestion of samples under the conditions of AOAC Method 2002.02 followed by the isolation and gravimetric procedures of AOAC Methods 985.29 and 991.43 results in quantitation of HMWDF. The filtrate from the quantitation of HMWDF is concentrated, deionized, concentrated again, and analyzed by LC to determine the LMWSDF, i.e., all nondigestible oligosaccharides of degree of polymerization > or =3. TDF is calculated as the sum of HMWDF and LMWSDF. Repeatability standard deviations (Sr) ranged from 0.41 to 1.43, and reproducibility standard deviations (S(R)) ranged from 1.18 to 5.44. These results are comparable to other official dietary fiber methods, and the method is recommended for adoption as Official First Action. PMID:20334184

  10. Determination of total dietary fiber (CODEX definition) by enzymatic-gravimetric method and liquid chromatography: collaborative study.

    PubMed

    McCleary, Barry V; DeVries, Jonathan W; Rader, Jeanne I; Cohen, Gerald; Prosky, Leon; Mugford, David C; Champ, Martine; Okuma, Kazuhiro

    2010-01-01

    A method for the determination of total dietary fiber (TDF), as defined by the CODEX Alimentarius, was validated in foods. Based upon the principles of AOAC Official Methods 985.29, 991.43, 2001.03, and 2002.02, the method quantitates high- and low-molecular-weight dietary fiber (HMWDF and LMWDF, respectively). In 2007, McCleary described a method of extended enzymatic digestion at 37 degrees C to simulate human intestinal digestion followed by gravimetric isolation and quantitation of HMWDF and the use of LC to quantitate low-molecular-weight soluble dietary fiber (LMWSDF). The method thus quantitates the complete range of dietary fiber components from resistant starch (by utilizing the digestion conditions of AOAC Method 2002.02) to digestion resistant oligosaccharides (by incorporating the deionization and LC procedures of AOAC Method 2001.03). The method was evaluated through an AOAC collaborative study. Eighteen laboratories participated with 16 laboratories returning valid assay data for 16 test portions (eight blind duplicates) consisting of samples with a range of traditional dietary fiber, resistant starch, and nondigestible oligosaccharides. The dietary fiber content of the eight test pairs ranged from 11.57 to 47.83%. Digestion of samples under the conditions of AOAC Method 2002.02 followed by the isolation and gravimetric procedures of AOAC Methods 985.29 and 991.43 results in quantitation of HMWDF. The filtrate from the quantitation of HMWDF is concentrated, deionized, concentrated again, and analyzed by LC to determine the LMWSDF, i.e., all nondigestible oligosaccharides of degree of polymerization > or =3. TDF is calculated as the sum of HMWDF and LMWSDF. Repeatability standard deviations (Sr) ranged from 0.41 to 1.43, and reproducibility standard deviations (S(R)) ranged from 1.18 to 5.44. These results are comparable to other official dietary fiber methods, and the method is recommended for adoption as Official First Action.

  11. [Evaluation of the AOAC 985.29 enzimic gravimetric method for determination of dietary fiber in oat and corn grains].

    PubMed

    da Silva, Leila Picolli; Ciocca, Maria de Lourdes Santorio; Furlong, Eliana Badiale

    2003-12-01

    The precision attributes and use of the enzymatic-gravimetric method of Prosky et al. (1992) (AOAC 985.29) were evaluated using corn (BR 5202 Pampa) and oat (UFRGS 15) samples. The effect of laboratory batches carried out in different days were evaluated in six laboratory batches, using for each material one duplicate for total fiber (FT) determination, one duplicate for insoluble fiber (FI) determination and blank ones for FT and for FI (both in duplicate). In order to characterize repetitive aspects, five other FT and FI determinations added to each sample were evaluated, summing up 11 data. The low coefficients of variation in the first six batches were considered acceptable as an expression of expected total intralaboratory variation. The repetitive of the method was considered good for FT determinations (CVs < 10%). However, in the FI determination a high frequency of negative values of ash and blanks was found, impairing the repetitive aspects evaluation. The magnitude of the total gravimetric corrections varies with the kind of the sample and is especially influenced by the protein content.

  12. Quantitative Hydrocarbon Energies from the PMO Method.

    ERIC Educational Resources Information Center

    Cooper, Charles F.

    1979-01-01

    Details a procedure for accurately calculating the quantum mechanical energies of hydrocarbons using the perturbational molecular orbital (PMO) method, which does not require the use of a computer. (BT)

  13. Determination of insoluble, soluble, and total dietary fiber (CODEX definition) by enzymatic-gravimetric method and liquid chromatography: collaborative study.

    PubMed

    McCleary, Barry V; DeVries, Jonathan W; Rader, Jeanne I; Cohen, Gerald; Prosky, Leon; Mugford, David C; Okuma, Kazuhiro

    2012-01-01

    A method for the determination of insoluble (IDF), soluble (SDF), and total dietary fiber (TDF), as defined by the CODEX Alimentarius, was validated in foods. Based upon the principles of AOAC Official Methods 985.29, 991.43, 2001.03, and 2002.02, the method quantitates water-insoluble and water-soluble dietary fiber. This method extends the capabilities of the previously adopted AOAC Official Method 2009.01, Total Dietary Fiber in Foods, Enzymatic-Gravimetric-Liquid Chromatographic Method, applicable to plant material, foods, and food ingredients consistent with CODEX Definition 2009, including naturally occurring, isolated, modified, and synthetic polymers meeting that definition. The method was evaluated through an AOAC/AACC collaborative study. Twenty-two laboratories participated, with 19 laboratories returning valid assay data for 16 test portions (eight blind duplicates) consisting of samples with a range of traditional dietary fiber, resistant starch, and nondigestible oligosaccharides. The dietary fiber content of the eight test pairs ranged from 10.45 to 29.90%. Digestion of samples under the conditions of AOAC 2002.02 followed by the isolation, fractionation, and gravimetric procedures of AOAC 985.29 (and its extensions 991.42 and 993.19) and 991.43 results in quantitation of IDF and soluble dietary fiber that precipitates (SDFP). The filtrate from the quantitation of water-alcohol-insoluble dietary fiber is concentrated, deionized, concentrated again, and analyzed by LC to determine the SDF that remains soluble (SDFS), i.e., all dietary fiber polymers of degree of polymerization = 3 and higher, consisting primarily, but not exclusively, of oligosaccharides. SDF is calculated as the sum of SDFP and SDFS. TDF is calculated as the sum of IDF and SDF. The within-laboratory variability, repeatability SD (Sr), for IDF ranged from 0.13 to 0.71, and the between-laboratory variability, reproducibility SD (SR), for IDF ranged from 0.42 to 2.24. The within

  14. Determination of insoluble, soluble, and total dietary fiber (CODEX definition) by enzymatic-gravimetric method and liquid chromatography: collaborative study.

    PubMed

    McCleary, Barry V; DeVries, Jonathan W; Rader, Jeanne I; Cohen, Gerald; Prosky, Leon; Mugford, David C; Okuma, Kazuhiro

    2012-01-01

    A method for the determination of insoluble (IDF), soluble (SDF), and total dietary fiber (TDF), as defined by the CODEX Alimentarius, was validated in foods. Based upon the principles of AOAC Official Methods 985.29, 991.43, 2001.03, and 2002.02, the method quantitates water-insoluble and water-soluble dietary fiber. This method extends the capabilities of the previously adopted AOAC Official Method 2009.01, Total Dietary Fiber in Foods, Enzymatic-Gravimetric-Liquid Chromatographic Method, applicable to plant material, foods, and food ingredients consistent with CODEX Definition 2009, including naturally occurring, isolated, modified, and synthetic polymers meeting that definition. The method was evaluated through an AOAC/AACC collaborative study. Twenty-two laboratories participated, with 19 laboratories returning valid assay data for 16 test portions (eight blind duplicates) consisting of samples with a range of traditional dietary fiber, resistant starch, and nondigestible oligosaccharides. The dietary fiber content of the eight test pairs ranged from 10.45 to 29.90%. Digestion of samples under the conditions of AOAC 2002.02 followed by the isolation, fractionation, and gravimetric procedures of AOAC 985.29 (and its extensions 991.42 and 993.19) and 991.43 results in quantitation of IDF and soluble dietary fiber that precipitates (SDFP). The filtrate from the quantitation of water-alcohol-insoluble dietary fiber is concentrated, deionized, concentrated again, and analyzed by LC to determine the SDF that remains soluble (SDFS), i.e., all dietary fiber polymers of degree of polymerization = 3 and higher, consisting primarily, but not exclusively, of oligosaccharides. SDF is calculated as the sum of SDFP and SDFS. TDF is calculated as the sum of IDF and SDF. The within-laboratory variability, repeatability SD (Sr), for IDF ranged from 0.13 to 0.71, and the between-laboratory variability, reproducibility SD (SR), for IDF ranged from 0.42 to 2.24. The within

  15. Blood Density Is Nearly Equal to Water Density: A Validation Study of the Gravimetric Method of Measuring Intraoperative Blood Loss.

    PubMed

    Vitello, Dominic J; Ripper, Richard M; Fettiplace, Michael R; Weinberg, Guy L; Vitello, Joseph M

    2015-01-01

    Purpose. The gravimetric method of weighing surgical sponges is used to quantify intraoperative blood loss. The dry mass minus the wet mass of the gauze equals the volume of blood lost. This method assumes that the density of blood is equivalent to water (1 gm/mL). This study's purpose was to validate the assumption that the density of blood is equivalent to water and to correlate density with hematocrit. Methods. 50 µL of whole blood was weighed from eighteen rats. A distilled water control was weighed for each blood sample. The averages of the blood and water were compared utilizing a Student's unpaired, one-tailed t-test. The masses of the blood samples and the hematocrits were compared using a linear regression. Results. The average mass of the eighteen blood samples was 0.0489 g and that of the distilled water controls was 0.0492 g. The t-test showed P = 0.2269 and R (2) = 0.03154. The hematocrit values ranged from 24% to 48%. The linear regression R (2) value was 0.1767. Conclusions. The R (2) value comparing the blood and distilled water masses suggests high correlation between the two populations. Linear regression showed the hematocrit was not proportional to the mass of the blood. The study confirmed that the measured density of blood is similar to water.

  16. Comprehensive measurement of total nondigestible carbohydrates in foods by enzymatic-gravimetric method and liquid chromatography.

    PubMed

    Nishibata, Toyohide; Tashiro, Kouichi; Kanahori, Sumiko; Hashizume, Chieko; Kitagawa, Machiko; Okuma, Kazuhiro; Gordon, Dennis T

    2009-09-01

    Total nondigestible carbohydrate (NDC) in foods was determined by combining, not modifications, AOAC Official Methods 991.43, 2001.03, and 2002.02. Total NDC included insoluble dietary fiber (IDF) + high-molecular-weight soluble dietary fiber (HMWSDF), nondigestible oligosaccharides (NDO) not precipitated in ethanol solution, and resistant starch (RS). Eight sources of NDC (cellulose, wheat bran, gum arabic, resistant maltodextrin, polydextrose, fructooligosaccharide, galactooligosaccharides, and RS) were incorporated in different combinations into standard formula bread samples. All of the NDC sources and bread samples were analyzed for their (1) IDF + HMWSDF content with corrections for residual RS amount using AOAC Official Method 991.43, (2) NDO by liquid chromatography (LC) in AOAC Official Method 2001.03, and (3) RS by AOAC Official Method 2002.02. The correlation coefficient (R(2)) comparing calculated amounts versus measured amounts of total NDC in 11 bread samples was 0.92. Analysis of commercial food samples was also well matched with the DF + NDO value on their nutritional label. Consequently, we confirmed a single measurement of LC can determine all NDO in foods, and total NDC in foods can be determined by unifying existing AOAC Official Methods.

  17. Methods of increasing hydrocarbon production from subterranean formations

    SciTech Connect

    Penny, G.S.; Briscoe, J.E.

    1982-01-10

    Methods of increasing hydrocarbon production from subterranean hydrocarbon-containing formations are provided. The formations are contacted with cationic perfluoro compounds. The formula for these compounds is given.

  18. Methods for dispersing hydrocarbons using autoclaved bacteria

    DOEpatents

    Tyndall, R.L.

    1996-11-26

    A method of dispersing a hydrocarbon includes the following steps: providing a bacterium selected from the following group: ATCC 85527, ATCC 75529, and ATCC 55638, a mutant of any one of these bacteria possessing all the identifying characteristics of any one of these bacteria, and mixtures; autoclaving the bacterium to derive a dispersant solution; and contacting the dispersant solution with a hydrocarbon to disperse the hydrocarbon. Moreover, a method for preparing a dispersant solution includes the following steps: providing a bacterium selected from the following group: ATCC 75527, ATCC 75529, and ATCC 55638, a mutant of any one of these bacteria possessing all the identifying characteristics of any one of these bacteria, and mixtures; and autoclaving the bacterium to derive a dispersant solution.

  19. Methods for dispersing hydrocarbons using autoclaved bacteria

    DOEpatents

    Tyndall, Richard L.

    1996-01-01

    A method of dispersing a hydrocarbon includes the steps: providing a bacterium selected from the following group: ATCC 85527, ATCC 75529, and ATCC 55638, a mutant of any one of these bacteria possessing all the identifying characteristics of any one of these bacteria, and mixtures thereof; autoclaving the bacterium to derive a dispersant solution therefrom; and contacting the dispersant solution with a hydrocarbon to disperse the hydrocarbon. Moreover, a method for preparing a dispersant solution includes the following steps: providing a bacterium selected from the following group: ATCC 75527, ATCC 75529, and ATCC 55638, a mutant of any one of these bacteria possessing all the identifying characteristics of any one of these bacteria, and mixtures thereof; and autoclaving the bacterium to derive a dispersant solution therefrom.

  20. Method of dispersing a hydrocarbon using bacteria

    DOEpatents

    Tyndall, R.L.

    1996-09-24

    A new protozoan derived microbial consortia and method for their isolation are provided. The isolated consortia and bacteria are useful for treating wastes such as trichloroethylene and trinitrotoluene. The isolated consortia, bacteria, and dispersants are useful for dispersing hydrocarbons such as oil, creosote, wax, and grease.

  1. Method of dispersing a hydrocarbon using bacteria

    DOEpatents

    Tyndall, Richard L.

    1996-01-01

    New protozoan derived microbial consortia and method for their isolation are provided. Consortia and bacteria isolated therefrom are useful for treating wastes such as trichloroethylene and trinitrotoluene. Consortia, bacteria isolated therefrom, and dispersants isolated therefrom are useful for dispersing hydrocarbons such as oil, creosote, wax, and grease.

  2. Conversion method for gas streams containing hydrocarbons

    DOEpatents

    Mallinson, Richard G.; Lobban, Lance; Liu, Chang-jun

    2000-01-01

    An apparatus and a method of using the apparatus are provided for converting a gas stream containing hydrocarbons to a reaction product containing effluent molecules having at least one carbon atom, having at least one interior surface and at least one exterior surface, a first electrode and a second electrode with the first and second electrodes being selectively movable in relation to each other and positioned within the housing so as to be spatially disposed a predetermined distance from each other, a plasma discharge generator between the first and second electrodes, gas stream introducer and a collector for collecting the reaction product effluent produced by the reaction of the gas stream containing hydrocarbons with the plasma discharge between the first and second electrodes.

  3. Method and apparatus for synthesizing hydrocarbons

    DOEpatents

    Colmenares, C.A.; Somorjai, G.A.; Maj, J.J.

    1983-06-21

    A method and apparatus for synthesizing a mixture of hydrocarbons having five carbons or less is disclosed. An equal molar ratio of CO and H/sub 2/ gases is caused to pass through a ThO/sub 2/ catalyst having a surface area of about 80 to 125 m/sup 2//g. The catalyst further includes Na present as a substitutional cation in an amount of about 5 to 10 atom %. At a temperature of about 340 to 360/sup 0/C, and at pressures of about 20 to 50 atm, CH/sub 3/OH is produced in an amount of about 90 wt % of the total hydrocarbon mixture, and comprised 1 mole % of the effluent gas.

  4. Method of increasing hydrocarbon production from subterranean formations

    SciTech Connect

    Penny, G.S.

    1987-10-27

    A method is described of increasing the production of hydrocarbons from a hydrocarbon-containing subterranean carbonate-containing formation comprising contacting the formation with an anionic compound whereby the compound is absorbed onto surfaces of the formation to reduce wetting of the surfaces by either hydrocarbons or water. The anionic compound is selected from individual compounds and mixtures.

  5. Method and apparatus for low temperature destruction of halogenated hydrocarbons

    DOEpatents

    Reagen, William Kevin; Janikowski, Stuart Kevin

    1999-01-01

    A method and apparatus for decomposing halogenated hydrocarbons are provided. The halogenated hydrocarbon is mixed with solvating agents and maintained in a predetermined atmosphere and at a predetermined temperature. The mixture is contacted with recyclable reactive material for chemically reacting with the recyclable material to create dehalogenated hydrocarbons and halogenated inorganic compounds. A feature of the invention is that the process enables low temperature destruction of halogenated hydrocarbons.

  6. Method and apparatus for synthesizing hydrocarbons

    DOEpatents

    Colmenares, C.A.; Somorjai, G.A.; Maj, J.J.

    1985-04-16

    A method and apparatus for synthesizing a mixture of aliphatic alcohols having five carbons or less is disclosed. An equal molar ratio of CO and H/sub 2/ gases is caused to pass through a ThO/sub 2/ catalyst having a surface area of about 80 to 125 m/sup 2//g. The catalyst further optionally includes Na ions present as substitutional cations in an amount of about 5 to 10 atom %. At a temperature of about 570 to 630/sup 0/K, and at pressures of about 20 to 50 atm, methanol and isobutanol are the predominant products and are produced in amounts of about 90 wt % of the total hydrocarbon mixture. 6 figs.

  7. Method and apparatus for fractionating hydrocarbon crudes

    SciTech Connect

    Harandi, M.N.

    1987-05-12

    A distillation method is described comprising: introducing heated hydrocarbon feed into a first distillation zone of a vacuum distillation means having first and second distillation zones physically separated from each other by divider means to cause a first separation of the feed into a descending liquid portion and an ascending vapor portion substantially all of the separated descending liquid remaining in the first distillation zone; withdrawing at least part of the liquid from the first distillation zone; reheating the withdrawn liquid portion; and introducing the reheated liquid portion into a second distillation zone which is part of the same distillation column as the first distillation zone, to cause a second separation of the reheated liquid portion into a descending liquid portion and an ascending vapor portion substantially all of the reheated, separated descending liquid remaining in the second distillation zone.

  8. A silica gel based method for extracting insect surface hydrocarbons.

    PubMed

    Choe, Dong-Hwan; Ramírez, Santiago R; Tsutsui, Neil D

    2012-02-01

    Here, we describe a novel method for the extraction of insect cuticular hydrocarbons using silica gel, herein referred to as "silica-rubbing". This method permits the selective sampling of external hydrocarbons from insect cuticle surfaces for subsequent analysis using gas chromatography-mass spectrometry (GC-MS). The cuticular hydrocarbons are first adsorbed to silica gel particles by rubbing the cuticle of insect specimens with the materials, and then are subsequently eluted using organic solvents. We compared the cuticular hydrocarbon profiles that resulted from extractions using silica-rubbing and solvent-soaking methods in four ant and one bee species: Linepithema humile, Azteca instabilis, Camponotus floridanus, Pogonomyrmex barbatus (Hymenoptera: Formicidae), and Euglossa dilemma (Hymenoptera: Apidae). We also compared the hydrocarbon profiles of Euglossa dilemma obtained via silica-rubbing and solid phase microextraction (SPME). Comparison of hydrocarbon profiles obtained by different extraction methods indicates that silica rubbing selectively extracts the hydrocarbons that are present on the surface of the cuticular wax layer, without extracting hydrocarbons from internal glands and tissues. Due to its surface specificity, efficiency, and low cost, this new method may be useful for studying the biology of insect cuticular hydrocarbons.

  9. Methods of increasing hydrocarbon production from subterranean formations

    SciTech Connect

    Penny, G.S.; Gardner, T.R.

    1986-04-29

    A method is described of increasing the production of hydrocarbons from a hydrocarbon-containing subterranean carbonate-containing formation comprising introducing into the subterranean formation an anionic perfluoro substituted compound in a liquid carrier fluid whereby the compound is absorbed onto surfaces of the formation to reduce wetting of the surfaces by either hydrocarbons or water, the anionic perfluoro substituted compound being selected from individual compounds and mixtures thereof.

  10. Methods for natural gas and heavy hydrocarbon co-conversion

    DOEpatents

    Kong, Peter C.; Nelson, Lee O.; Detering, Brent A.

    2009-02-24

    A reactor for reactive co-conversion of heavy hydrocarbons and hydrocarbon gases and includes a dielectric barrier discharge plasma cell having a pair of electrodes separated by a dielectric material and passageway therebetween. An inlet is provided for feeding heavy hydrocarbons and other reactive materials to the passageway of the discharge plasma cell, and an outlet is provided for discharging reaction products from the reactor. A packed bed catalyst may optionally be used in the reactor to increase efficiency of conversion. The reactor can be modified to allow use of a variety of light sources for providing ultraviolet light within the discharge plasma cell. Methods for upgrading heavy hydrocarbons are also disclosed.

  11. Substantially self-powered method and apparatus for recovering hydrocarbons from hydrocarbon-containing solid hydrates

    DOEpatents

    Elliott, G.R.B.; Barraclough, B.L.; Vanderborgh, N.E.

    1981-02-19

    A method and apparatus are provided for producing gaseous hydrocarbons from formations comprising solid hydrocarbon hydrates located under either a body of land or a body of water. The vast natural resources of such hydrocarbon hydrates can thus now be economically mined. Relatively warm brine or water is brought down from an elevation above that of the hydrates through a portion of the apparatus, and passes in contact with the hydrates, thus melting them. The liquid then continues up another portion of the apparatus carrying entrained hydrocarbon vapors in the form of bubbles, which can easily be separated from the liquid. After a short startup procedure, the process and apparatus are substantially self-powered.

  12. Substantially self-powered method and apparatus for recovering hydrocarbons from hydrocarbon-containing solid hydrates

    DOEpatents

    Elliott, Guy R. B.; Barraclough, Bruce L.; Vanderborgh, Nicholas E.

    1983-01-01

    A method and apparatus are provided for producing gaseous hydrocarbons from formations comprising solid hydrocarbon hydrates located under either a body of land or a body of water. The vast natural resources of such hydrocarbon hydrates can thus now be economically mined. Relatively warm brine or water is brought down from an elevation above that of the hydrates through a portion of the apparatus and passes in contact with the hydrates, thus melting them. The liquid then continues up another portion of the apparatus, carrying entrained hydrocarbon vapors in the form of bubbles, which can easily be separated from the liquid. After a short startup procedure, the process and apparatus are substantially self-powered.

  13. Catalysts for converting syngas into liquid hydrocarbons and methods thereof

    DOEpatents

    Yu, Fei; Yan, Qiangu; Batchelor, William

    2016-03-15

    The presently-disclosed subject matter includes methods for producing liquid hydrocarbons from syngas. In some embodiments the syngas is obtained from biomass and/or comprises a relatively high amount of nitrogen and/or carbon dioxide. In some embodiments the present methods can convert syngas into liquid hydrocarbons through a one-stage process. Also provided are catalysts for producing liquid hydrocarbons from syngas, wherein the catalysts include a base material, a transition metal, and a promoter. In some embodiments the base material includes a zeolite-iron material or a cobalt-molybdenum carbide material. In still further embodiments the promoter can include an alkali metal.

  14. Method and apparatus for detecting gem-polyhalogenated hydrocarbons

    DOEpatents

    Anderson, deceased, William G.; Anderson, legal representative, Johanna S.

    1990-01-01

    A method and optrode for detecting gem polyhalogenated hydrocarbons in a sample fluid based on a single phase Fujiwara reaction as provided. The method comprises contacting a reaction mixture with a sample fluid which contains the gem-polyhalogenated hydrocarbons. The reaction mixture comprises an aqueous solution of pyridine or derivative thereof and a hindered nitrogen base. Upon contact a fluorescent and/or chromgenic reaction product forms whose fluorescence and/or absorbance is related to the concentration of gem-polyhalogenated hydrocarbons in the sample fluid.

  15. Method for making hydrogen rich gas from hydrocarbon fuel

    DOEpatents

    Krumpelt, M.; Ahmed, S.; Kumar, R.; Doshi, R.

    1999-07-27

    A method of forming a hydrogen rich gas from a source of hydrocarbon fuel in which the hydrocarbon fuel contacts a two-part catalyst comprising a dehydrogenation portion and an oxide-ion conducting portion at a temperature not less than about 400 C for a time sufficient to generate the hydrogen rich gas while maintaining CO content less than about 5 volume percent. There is also disclosed a method of forming partially oxidized hydrocarbons from ethanes in which ethane gas contacts a two-part catalyst comprising a dehydrogenation portion and an oxide-ion conducting portion for a time and at a temperature sufficient to form an oxide. 4 figs.

  16. Method for making hydrogen rich gas from hydrocarbon fuel

    DOEpatents

    Krumpelt, Michael; Ahmed, Shabbir; Kumar, Romesh; Doshi, Rajiv

    1999-01-01

    A method of forming a hydrogen rich gas from a source of hydrocarbon fuel in which the hydrocarbon fuel contacts a two-part catalyst comprising a dehydrogenation portion and an oxide-ion conducting portion at a temperature not less than about 400.degree. C. for a time sufficient to generate the hydrogen rich gas while maintaining CO content less than about 5 volume percent. There is also disclosed a method of forming partially oxidized hydrocarbons from ethanes in which ethane gas contacts a two-part catalyst comprising a dehydrogenation portion and an oxide-ion conducting portion for a time and at a temperature sufficient to form an oxide.

  17. Hydrocarbons from plants: Analytical methods and observations

    SciTech Connect

    Calvin, Melvin

    1980-11-01

    We have suggested that certain plants rich in hydrocarbon-like materials might be cultivated for renewable photosynthetic products. Two species were selected for experimental plantations: Euphorbia lathyris, an annual from seed and Euphorbia tirucalli, a perennial from cuttings, The yield from each species is over 10 barrels of oil/acre/year without genetic or agronomic improvement. In addition to plants, there are trees, such as species of Copaifera in Brazil and other tropical areas, which produce a diesel-like oil upon tapping. Each tree produces approximately 40 liters of hydrocarbon per year, and this material can be used directly by a diesel-powered car. Further efforts to develop plants as alternate energy sources are underway, as well as a continuing search for additional plant species throughout the world which have a similar capability.

  18. Geological effect of high-precise gravimetric and magnetic surveys in Yangqiao prospect in Biyang depression

    SciTech Connect

    Rongyuan, W.; Zhaoling, Y.; Zhangmin, G.; Xiaoliu, W. )

    1991-01-01

    This paper reports on Yangqiao prospect in Biyang depression which is an area where very high-degree exploration has been done. The complicated seismic and geological conditions in the border area of the depression cause very poor seismic data, so that exact structural configuration can not be known. Thus, high-precise gravimetric-magnetic surveys were done. The interpretations of gravimetric and magnetic data are mainly based on the properties of gravitational and magnetic fields. Local gravimetric and magnetic anomalies at Wangzhuang were discovered by performing forward fitting of observed gravimetric and magnetic data. The repeated seismic interpretation by reference to the gravimetric-magnetic interpretation result confirms the existence of an anticline structure in the local gravimetric and magnetic anomaly area. The effect of direct hydrocarbon prediction using high- precise gravimetric and magnetic data were checked in known Anpeng and Xiaermen oil fields. The check shows good effect.

  19. Comparison of a direct-reading device to gravimetric methods for evaluating organic dust aerosols in an enclosed swine production environment.

    PubMed

    Taylor, C D; Reynolds, S J

    2001-01-01

    The production of livestock in enclosed facilities has become an accepted practice, driven by the need for increased efficiency. Exposure to organic dusts, containing various bioactive components, has been identified an important risk factor for the high rate of lung disease found among workers in these environments. Assessment of organic dust exposure requires technical skills and instrumentation not readily available to most agricultural enterprises. Development of a simple, cost-effective method for measuring organic dust levels would be useful in evaluating and controlling exposures in these environments. The objective of this study was to evaluate the usefulness of the direct reading MIE PDM-3 Miniram for estimating organic dust concentrations in enclosed swine production facilities. Responses from the MIE PDM-3 Miniram were compared to gravimetric methods for total and inhalable dust. Total dust determinations were conducted in accordance with the National Institute for Occupational Safety and Health (NIOSH) method 0500. Inhalable particulate mass (IPM) sampling was conducted using SKC brand IOM (Institute of Occupational Medicine) sampling cassettes, which meet the American Conference of Governmental Industrial Hygienists ACGIH criteria for inhalable dust sampling. This study design also allowed for the comparison of traditional total dust method to the IPM method, in collecting organic dusts in an agricultural setting. Fifteen sets of side-by-side samples (Miniram, total dust, and IPM) were collected over a period of six months in a swine confinement building. There were statistically significant differences in the results provided by the three sampling methods. Measurements for inhalable dust exceeded those for total dust in eleven of fifteen samples. The Miniram time-weighted average (TWA) response to the organic dust was always the lower of the three methods. A high degree of correlation was found among all three methods. The Miniram performed well under

  20. Hydrocarbon synthesis catalyst and method of preparation

    DOEpatents

    Sapienza, Richard S.; Sansone, Michael J.; Slegeir, William A. R.

    1983-08-02

    A catalyst for the synthesis of hydrocarbons from carbon monoxide and hydrogen composed of palladium or platinum and cobalt supported on a solid phase is disclosed. The catalyst is prepared by heating a heterogeneous component of the palladium or platinum deposited on the solid support in a solution of cobalt carbonyl or precursors thereof. The catalyst exhibits excellent activity, stability in air, and produces highly desirable product fractions even with dilute gaseous reactants. The catalyst is preferably used in dilute slurry form, which is desirable from a heat transfer standpoint.

  1. Hydrocarbon synthesis catalyst and method of preparation

    DOEpatents

    Sapienza, R.S.; Sansone, M.J.; Slegeir, W.A.R.

    1983-08-02

    A catalyst for the synthesis of hydrocarbons from carbon monoxide and hydrogen composed of palladium or platinum and cobalt supported on a solid phase is disclosed. The catalyst is prepared by heating a heterogeneous component of the palladium or platinum deposited on the solid support in a solution of cobalt carbonyl or precursors thereof. The catalyst exhibits excellent activity, stability in air, and produces highly desirable product fractions even with dilute gaseous reactants. The catalyst is preferably used in dilute slurry form, which is desirable from a heat transfer standpoint. 9 figs.

  2. Method for coupling a hydrocarbon containing molecular species

    SciTech Connect

    Lingwood, C.A.

    1986-07-01

    A method is described of covalently coupling two molecular species comprising: (a) combining (i) a first molecular species having a functionality reactive with hydrocarbon when photo-activated; and (ii) a solution of at least one, hydrocarbon containing, molecular species in the absence of photo-radiation to which the functionality is sensitive; (b) removing the solvent; (c) irradiating the mixture with photo-radiation to which the functionality is photosensitive.

  3. Method and apparatus for detecting halogenated hydrocarbons

    DOEpatents

    Monagle, Matthew; Coogan, John J.

    1997-01-01

    A halogenated hydrocarbon (HHC) detector is formed from a silent discharge (also called a dielectric barrier discharge) plasma generator. A silent discharge plasma device receives a gas sample that may contain one or more HHCs and produces free radicals and excited electrons for oxidizing the HHCs in the gas sample to produce water, carbon dioxide, and an acid including halogens in the HHCs. A detector is used to sensitively detect the presence of the acid. A conductivity cell detector combines the oxidation products with a solvent where dissociation of the acid increases the conductivity of the solvent. The conductivity cell output signal is then functionally related to the presence of HHCs in the gas sample. Other detectors include electrochemical cells, infrared spectrometers, and negative ion mobility spectrometers.

  4. Modelling the density contrast and depth of the Moho discontinuity by seismic and gravimetric-isostatic methods with an application to Africa

    NASA Astrophysics Data System (ADS)

    Bagherbandi, Mohammad; Sjöberg, Lars E.

    2012-06-01

    The crustal thickness (Moho depth) is of interest in several geosciences applications, such as geography, geophysics and geodesy. Usually the crustal depth and density variations are estimated by seismic survey data. As such data collection is very time-consuming and expensive an attractive option could be to use a gravimetric/isostatic model. In this case, realistic estimates for the crustal density and Moho density contrast (MDC) are important. In this study, we first use the seismic crustal thickness of CRUST2.0 model as a known parameter in combination with gravimetric data in estimating the crust-mantle density contrast by the isostatic model of Vening Meinesz-Moritz. We present different models to estimate the MDC and its impact on the modelling of the gravimetric-isostatic Moho depth. The theory is applied to estimate the Moho depth of the African continental crust by using different models for the MDC: (a) constant value (0.6 g/cm3), (b) Pratt-Hayford's model, (c) CRUST2.0 as input to three gravimetric/isostatic models based on Vening Meinesz-Moritz theory. The isostatic models agree by 5.8-7.1 km in the rms with the regional seismic model at a resolution of 2° × 2°, and the smallest rms difference at a resolution of 1° × 1° is of 7.2 km. For comparison, the rms differences of CRUST2.0 and the regional seismic model are 8.8 and 9.1 km at the resolutions of 2° (interpolated) and 1°, respectively. The result suggests that the gravimetric/isostatic Moho model can be used in densification of the CRUST2.0 Moho geometry, and to improve it in areas with poor data.

  5. Gravimetric gas determinations for volume calibrations

    SciTech Connect

    Gibbs, P.W.

    1991-01-01

    Gravimetric measurement of gases is one of the methods available for calibrating gas volumes. By inputting a known quantity of gas and measuring the resulting pressure and temperature, the system volume can be calculated using gas law principles. Historically, this method has been less accurate due to the difficulty in the mass determination. This difficulty comes from several sources. Two examples are the large tare weight of the gas container relative to the weight of gas and the external volume of the gas container relative to the standards. The application of a gravimetric gas determination to tank volume calibrations at the Savannah River Site is discussed. Mass determinations on a 25,000 gram gas container were such that a 1500 gram quantity of gas was routinely determined to within {plus minus}0.2 gram at the 99% confidence level. The weighing design and the methods used to address the difficulties of the mass determination are detailed.

  6. Gravimetric determination of phospholipid concentration.

    PubMed

    Tejera-Garcia, Roberto; Connell, Lisa; Shaw, Walter A; Kinnunen, Paavo K J

    2012-09-01

    Accurate determination of lipid concentrations is an obligatory routine in a research laboratory engaged in studies using this class of biomaterials. For phospholipids, this is frequently accomplished using the phosphate assay (Bartlett, G.R. Phosphorus Assay in Column Chromatography. J. Biol. Chem. 234, 466-468, 1959). Given the purity of the currently commercially available synthetic and isolated natural lipids, we have observed that determination of the dry weight of lipid stock solutions provides the fastest, most accurate, and generic method to assay their concentrations. The protocol described here takes advantage of the high resolution and accuracy obtained by modern weighing technology. We assayed by this technique the concentrations of a number of phosphatidylcholine samples, with different degrees of acyl chain saturation and length, and in different organic solvents. The results were compared with those from Bartlett assay, (31)P NMR, and Langmuir compression isotherms. The data obtained show that the gravimetric assay yields lipid concentrations with a resolution similar or better than obtained by the other techniques.

  7. Method for recovering light hydrocarbons from coal agglomerates

    DOEpatents

    Huettenhain, Horst; Benz, August D.; Getsoian, John

    1991-01-01

    A method and apparatus for removing light hydrocarbons, such as heptane, from coal agglomerates includes an enclosed chamber having a substantially horizontal perforate surface therein. The coal agglomerates are introduced into a water bath within the chamber. The agglomerates are advanced over the surface while steam is substantially continuously introduced through the surface into the water bath. Steam heats the water and causes volatilization of the light hydrocarbons, which may be collected from the overhead of the chamber. The resulting agglomerates may be collected at the opposite end from the surface and subjected to final draining processes prior to transportation or use.

  8. Method for determining processability of a hydrocarbon containing feedstock

    SciTech Connect

    Schabron, John F.; Rovani, Jr., Joseph F.

    2013-09-10

    Disclosed herein is a method involving the steps of (a) precipitating an amount of asphaltenes from a liquid sample of a first hydrocarbon-containing feedstock having solvated asphaltenes therein with one or more first solvents in a column; (b) determining one or more solubility characteristics of the precipitated asphaltenes; (c) analyzing the one or more solubility characteristics of the precipitated asphaltenes; and (d) correlating a measurement of feedstock reactivity for the first hydrocarbon-containing feedstock sample with a mathematical parameter derived from the results of analyzing the one or more solubility characteristics of the precipitated asphaltenes.

  9. Method and apparatus for producing oxygenates from hydrocarbons

    DOEpatents

    Kong, Peter C.; Lessing, Paul A.

    1995-01-01

    A chemical reactor for oxygenating hydrocarbons includes: a) a dielectric barrier discharge plasma cell, the plasma cell comprising a pair of electrodes having a dielectric material and void therebetween, the plasma cell comprising a hydrocarbon gas inlet feeding to the void; b) a solid oxide electrochemical cell, the electrochemical cell comprising a solid oxide electrolyte positioned between a porous cathode and a porous anode, an oxygen containing gas inlet stream feeding to the porous cathode side of the electrochemical cell; c) a first gas passageway feeding from the void to the anode side of the electrochemical cell; and d) a gas outlet feeding from the anode side of the electrochemical cell to expel reaction products from the chemical reactor. A method of oxygenating hydrocarbons is also disclosed.

  10. Method and apparatus for producing oxygenates from hydrocarbons

    DOEpatents

    Kong, P.C.; Lessing, P.A.

    1995-06-27

    A chemical reactor for oxygenating hydrocarbons includes: (a) a dielectric barrier discharge plasma cell, the plasma cell comprising a pair of electrodes having a dielectric material and void therebetween, the plasma cell comprising a hydrocarbon gas inlet feeding to the void; (b) a solid oxide electrochemical cell, the electrochemical cell comprising a solid oxide electrolyte positioned between a porous cathode and a porous anode, an oxygen containing gas inlet stream feeding to the porous cathode side of the electrochemical cell; (c) a first gas passageway feeding from the void to the anode side of the electrochemical cell; and (d) a gas outlet feeding from the anode side of the electrochemical cell to expel reaction products from the chemical reactor. A method of oxygenating hydrocarbons is also disclosed. 4 figs.

  11. Chromatographic methods for carcinogenic/mutagenic nitropolycyclic aromatic hydrocarbons.

    PubMed

    Hayakawa, K

    2000-10-01

    Nitropolycyclic aromatic hydrocarbons (NPAHs), which are known to be carcinogenic and/or mutagenic, are considered to be one of the air pollutants that cause lung cancer. In the last two decades, a number of sensitive and selective methods have been developed for the determination of NPAHs and related compounds in environmental and biological samples. This paper describes the state of the art of the methods and applications. PMID:11002277

  12. Method for production of hydrocarbons from hydrates

    DOEpatents

    McGuire, Patrick L.

    1984-01-01

    A method of recovering natural gas entrapped in frozen subsurface gas hydrate formations in arctic regions. A hot supersaturated solution of CaCl.sub.2 or CaBr.sub.2, or a mixture thereof, is pumped under pressure down a wellbore and into a subsurface hydrate formation so as to hydrostatically fracture the formation. The CaCl.sub.2 /CaBr.sub.2 solution dissolves the solid hydrates and thereby releases the gas entrapped therein. Additionally, the solution contains a polymeric viscosifier, which operates to maintain in suspension finely divided crystalline CaCl.sub.2 /CaBr.sub.2 that precipitates from the supersaturated solution as it is cooled during injection into the formation.

  13. Future Directions of Electromagnetic Methods for Hydrocarbon Applications

    NASA Astrophysics Data System (ADS)

    Strack, K. M.

    2014-01-01

    For hydrocarbon applications, seismic exploration is the workhorse of the industry. Only in the borehole, electromagnetic (EM) methods play a dominant role, as they are mostly used to determine oil reserves and to distinguish water from oil-bearing zones. Throughout the past 60 years, we had several periods with an increased interest in EM. This increased with the success of the marine EM industry and now electromagnetics in general is considered for many new applications. The classic electromagnetic methods are borehole, onshore and offshore, and airborne EM methods. Airborne is covered elsewhere (see Smith, this issue). Marine EM material is readily available from the service company Web sites, and here I will only mention some future technical directions that are visible. The marine EM success is being carried back to the onshore market, fueled by geothermal and unconventional hydrocarbon applications. Oil companies are listening to pro-EM arguments, but still are hesitant to go through the learning exercises as early adopters. In particular, the huge business drivers of shale hydrocarbons and reservoir monitoring will bring markets many times bigger than the entire marine EM market. Additional applications include support for seismic operations, sub-salt, and sub-basalt, all areas where seismic exploration is costly and inefficient. Integration with EM will allow novel seismic methods to be applied. In the borehole, anisotropy measurements, now possible, form the missing link between surface measurements and ground truth. Three-dimensional (3D) induction measurements are readily available from several logging contractors. The trend to logging-while-drilling measurements will continue with many more EM technologies, and the effort of controlling the drill bit while drilling including look-ahead-and-around the drill bit is going on. Overall, the market for electromagnetics is increasing, and a demand for EM capable professionals will continue. The emphasis will

  14. Expressions for the Global Gravimetric Moho Modeling in Spectral Domain

    NASA Astrophysics Data System (ADS)

    Tenzer, Robert; Chen, Wenjin

    2014-08-01

    We apply a newly developed numerical method to improve the Moho geometry by the implementation of gravity data. This method utilizes expressions for the gravimetric forward and inverse modeling derived in a frequency domain. Methods for a spectral analysis and synthesis of the gravity field and crust density structures are applied in the gravimetric forward modeling of the consolidated crust-stripped gravity disturbances, which have a maximum correlation with the (a priori) Moho model. These gravity disturbances are obtained from the Earth's gravity disturbances after applying the topographic and stripping gravity corrections of major known anomalous crust density structures; in the absence of a global mantle model, mantle density heterogeneities are disregarded. The isostatic scheme applied is based on a complete compensation of the crust relative to the upper mantle density. The functional relation is established between the (unknown) Moho depths and the complete crust-stripped isostatic gravity disturbances, which according to the adopted isostatic scheme have (theoretically) a minimum correlation with the Moho geometry. The system of observation equations, which describes the relation between spherical functions of the isostatic gravity field and the Moho geometry, is defined by means of a linearized Fredholm integral equation of the first kind. The Moho depths are determined based on solving the gravimetric inverse problem. The regularization is applied to stabilize the ill-posed solution. This numerical procedure is utilized to determine the Moho depths globally. The gravimetric result is presented and compared with the seismic Moho model. Our gravimetric result has a relatively good agreement with the CRUST2.0 Moho model by means of the RMS of differences (of 3.5 km). However, the gravimetric solution has a systematic bias. We explain this bias between the gravimetric and seismic Moho models by the unmodelled mantle heterogeneities and uncertainties in the

  15. Method for recovering hydrocarbons from molten metal halides

    DOEpatents

    Pell, Melvyn B.

    1979-01-01

    In a process for hydrocracking heavy carbonaceous materials by contacting such carbonaceous materials with hydrogen in the presence of a molten metal halide catalyst to produce hydrocarbons having lower molecular weights and thereafter recovering the hydrocarbons so produced from the molten metal halide, an improvement comprising injecting into the spent molten metal halide, a liquid low-boiling hydrocarbon stream is disclosed.

  16. Method for removing chlorine compounds from hydrocarbon mixtures

    DOEpatents

    Janoski, Edward J.; Hollstein, Elmer J.

    1985-12-31

    A process for removing halide ions from a hydrocarbon feedstream containing halogenated hydrocarbons wherein the contaminated feedstock is contacted with a solution of a suitable oxidizing acid containing a lanthanide oxide, the acid being present in a concentration of at least about 50 weight percent for a time sufficient to remove substantially all of the halide ion from the hydrocarbon feedstock.

  17. Method for removing chlorine compounds from hydrocarbon mixtures

    DOEpatents

    Janoski, E.J.; Hollstein, E.J.

    1984-09-29

    A process for removing halide ions from a hydrocarbon feedstream containing halogenated hydrocarbons wherein the contaminated feedstock is contacted with a solution of a suitable oxidizing acid containing a lanthanide oxide, the acid being present in a concentration of at least about 50 weight percent for a time sufficient to remove substantially all of the halide ion from the hydrocarbon feedstock.

  18. Method for the drying and removal of hydrocarbons from gases

    SciTech Connect

    Schlicht, B.S.; Beise, H.; Burk, W.; Gross, M.; Lindner, O.; Minak, H.; Sonntag, C.; Wehner, K.

    1984-10-30

    The invention relates to a method for the drying and removal of hydrocarbons from gases. It is the object of the invention to increase the absorption ability of the solvent for aromatic hydrocarbons including naphthalene and water, to save material and energy, to lower the investment- and operating costs, as well as to avoid operational disturbances and to increase the safety during gas treatment, gas transmittance and gas distribution. This object is accomplished by the invention in that a mixture of glycol, N-methyl-e-caprolactam and water is used as solvent. The mixture comprises 79.9 to 97 percent by weight of glycol, 2 to 20 percent by weight of N-methyl-e-caprolactam and 0.1 to 1 percent by weight of water. The regeneration temperature of the charged solvent mixture is 150/sup 0/ to 190/sup 0/ C., preferably 170/sup 0/ C. 3 to 15 percent by weight, preferably 10 percent by weight, of crude benzene is added to the charged solvent mixture. The invention is especially useful for the purification and drying of coal degasification and cracking gases in customary absorption and desorption apparatuses.

  19. Method for converting coal to hydrocarbons by hydrogenation

    SciTech Connect

    Koch, K.

    1982-08-17

    A method and apparatus are disclosed for converting, i.e. hydrogenating, dry particles of coal with hydrogen to give hydrocarbons such as engine or heating fuels. The invention combines together several steps in the hydrogenation process, such as compressing the dry coal, heating, plasticizing and hydrogenating, in one apparatus. The apparatus comprises a housing, preferably a cylinder containing a feed and preparation portion of a chamber with a rotatable friction element therein and an immediately adjoining hydrogenation portion of the chamber with a rotating rotor therein and with static mixing nozzles projecting thereinto, through which nozzles heated hydrogen can be injected into the coal which has been brought, by the friction element into a heated, plastic state. The friction element and rotor can be driven by a single drive means, the feed and preparation portion of the chamber can be fed with coal from a hopper through a wheel lock and the hydrocarbon products can be ejected through a valve into a separator.

  20. Solution mining systems and methods for treating hydrocarbon containing formations

    SciTech Connect

    Vinegar, Harold J.; de Rouffignac, Eric Pierre; Schoeling, Lanny Gene

    2009-07-14

    A method for treating an oil shale formation comprising nahcolite is disclosed. The method includes providing a first fluid to a portion of the formation through at least two injection wells. A second fluid is produced from the portion through at least one injection well until at least two injection wells are interconnected such that fluid can flow between the two injection wells. The second fluid includes at least some nahcolite dissolved in the first fluid. The first fluid is injected through one of the interconnected injection wells. The second fluid is produced from at least one of the interconnected injection wells. Heat is provided from one or more heaters to the formation to heat the formation. Hydrocarbon fluids are produced from the formation.

  1. Novel method for cleaning a vacuum chamber from hydrocarbon contamination

    SciTech Connect

    Wanzenboeck, H. D.; Roediger, P.; Hochleitner, G.; Bertagnolli, E.; Buehler, W.

    2010-11-15

    A novel method for cleaning a high vacuum chamber is presented. This method is based on concurrent in situ high-energetic UV light activation of contaminants located in the residual gas and at the vacuum chamber surfaces as well as the in situ generation of highly reactive ozone. Ozone oxidizes the contaminants to volatile species. Investigations by energy-dispersive x-ray analysis of residual gas depositions and mass-spectroscopy measurements of the residual gas in the vacuum chamber identify the contaminant species as hydrocarbons. After a cleaning period of 8 h, a decrease in measured chamber contamination by about 90% could be achieved according to atomic force microscope analysis. Mass spectroscopy measurements using a residual gas analyzer indicate the creation of volatile, carbonaceous species during the cleaning process.

  2. Downhole fluid injection systems, CO2 sequestration methods, and hydrocarbon material recovery methods

    DOEpatents

    Schaef, Herbert T.; McGrail, B. Peter

    2015-07-28

    Downhole fluid injection systems are provided that can include a first well extending into a geological formation, and a fluid injector assembly located within the well. The fluid injector assembly can be configured to inject a liquid CO2/H2O-emulsion into the surrounding geological formation. CO2 sequestration methods are provided that can include exposing a geological formation to a liquid CO2/H2O-emulsion to sequester at least a portion of the CO2 from the emulsion within the formation. Hydrocarbon material recovery methods are provided that can include exposing a liquid CO2/H2O-emulsion to a geological formation having the hydrocarbon material therein. The methods can include recovering at least a portion of the hydrocarbon material from the formation.

  3. Method for producing hydrocarbon and alcohol mixtures. [Patent application

    DOEpatents

    Compere, A.L.; Googin, J.M.; Griffith, W.L.

    1980-12-01

    It is an object of this invention to provide an efficient process for extracting alcohols and ketones from an aqueous solution containing the same into hydrocarbon fuel mixtures, such as gasoline, diesel fuel and fuel oil. Another object of the invention is to provide a mixture consisting of hydrocarbon, alcohols or ketones, polyoxyalkylene polymer and water which can be directly added to fuels or further purified. The above stated objects are achieved in accordance with a preferred embodiment of the invention by contacting an aqueous fermentation liquor with a hydrocarbon or hydrocarbon mixture containing carbon compounds having 5 to 18 carbon atoms, which may include gasoline, diesel fuel or fuel oil. The hydrocarbon-aqueous alcohol solution is mixed in the presence or one or more of a group of polyoxyalkylene polymers described in detail hereinafter; the fermentation alcohol being extracted into the hydrocarbon fuel-polyoxyalkylene polymer mixture.

  4. Method and apparatus for hydrocarbon recovery from tar sands

    DOEpatents

    Westhoff, James D.; Harak, Arnold E.

    1989-01-01

    A method and apparatus for utilizing tar sands having a broad range of bitumen content is disclosed. More particularly, tar sands are pyrolyzed in a cyclone retort with high temperature gases recycled from the cyclone retort to produce oil and hydrocarbon products. The spent tar sands are then burned at 2000.degree. F. in a burner to remove residual char and produce a solid waste that is easily disposable. The process and apparatus have the advantages of being able to utilize tar sands having a broad range of bitumen content and the advantage of producing product gases that are free from combustion gases and thereby have a higher heating value. Another important advantage is rapid pyrolysis of the tar sands in the cyclone so as to effectively utilize smaller sized reactor vessels for reducing capitol and operating costs.

  5. Method and apparatus for hydrocarbon recovery from tar sands

    DOEpatents

    Westhoff, J.D.; Harak, A.E.

    1988-05-04

    A method and apparatus for utilizing tar sands having a broad range of bitumen content is disclosed. More particularly, tar sands are pyrolyzed in a cyclone retort with high temperature gases recycled from the cyclone retort to produce oil and hydrocarbon products. The spent tar sands are then burned at 2000/degree/F in a burner to remove residual char and produce a solid waste that is easily disposable. The process and apparatus have the advantages of being able to utilize tar sands having a broad range of bitumen content and the advantage of producing product gases that are free from combustion gases and thereby have a higher heating value. Another important advantage is rapid pyrolysis of the tar sands in the cyclone so as to effectively utilize smaller sized reactor vessels for reducing capitol and operating costs. 1 fig., 1 tab.

  6. Systems and methods for producing hydrocarbons from tar sands formations

    DOEpatents

    Li, Ruijian; Karanikas, John Michael

    2009-07-21

    A system for treating a tar sands formation is disclosed. A plurality of heaters are located in the formation. The heaters include at least partially horizontal heating sections at least partially in a hydrocarbon layer of the formation. The heating sections are at least partially arranged in a pattern in the hydrocarbon layer. The heaters are configured to provide heat to the hydrocarbon layer. The provided heat creates a plurality of drainage paths for mobilized fluids. At least two of the drainage paths converge. A production well is located to collect and produce mobilized fluids from at least one of the converged drainage paths in the hydrocarbon layer.

  7. Apparatus and method for rapid separation and detection of hydrocarbon fractions in a fluid stream

    SciTech Connect

    Sluder, Charles S.; Storey, John M.; Lewis, Sr., Samuel A.

    2013-01-22

    An apparatus and method for rapid fractionation of hydrocarbon phases in a sample fluid stream are disclosed. Examples of the disclosed apparatus and method include an assembly of elements in fluid communication with one another including one or more valves and at least one sorbent chamber for removing certain classifications of hydrocarbons and detecting the remaining fractions using a detector. The respective ratios of hydrocarbons are determined by comparison with a non separated fluid stream.

  8. An improved gravimetric measure of cerebral edema.

    PubMed

    Marmarou, A; Tanaka, K; Shulman, K

    1982-02-01

    Significant errors are introduced into the measurement of brain tissue water by the specific gravity technique when the edema fluid contains protein. Protein adds to the tissue solids, increasing the density of the tissue, and masks the proportional increase of brain water. Existing equations relating measured specific gravity and tissue water are not applicable, and a new formula was developed that compensates for the protein component of edema and reduces the experimental error. The new method was applied to the measurement of tissue water in cat brain made edematous by direct infusion of fluids of known composition and volume to test the theory. This technique for improving the gravimetric assessment of brain edema is presented.

  9. Method for direct production of carbon disulfide and hydrogen from hydrocarbons and hydrogen sulfide feedstock

    SciTech Connect

    Miao, Frank Q.; Erekson, Erek James

    1998-12-01

    A method for converting hydrocarbons and hydrogen sulfide to carbon disulfide and hydrogen is provided comprising contacting the hydrocarbons and hydrogen sulfide to a bi-functional catalyst residing in a controlled atmosphere for a time and at a temperature sufficient to produce carbon disulfide and hydrogen. Also provided is a catalyst for converting carbon sulfides and hydrogen sulfides to gasoline range hydrocarbons comprising a mixture containing a zeolite catalyst and a hydrogenating catalyst.

  10. Method and apparatus for monitoring a hydrocarbon-selective catalytic reduction device

    DOEpatents

    Schmieg, Steven J; Viola, Michael B; Cheng, Shi-Wai S; Mulawa, Patricia A; Hilden, David L; Sloane, Thompson M; Lee, Jong H

    2014-05-06

    A method for monitoring a hydrocarbon-selective catalytic reactor device of an exhaust aftertreatment system of an internal combustion engine operating lean of stoichiometry includes injecting a reductant into an exhaust gas feedstream upstream of the hydrocarbon-selective catalytic reactor device at a predetermined mass flowrate of the reductant, and determining a space velocity associated with a predetermined forward portion of the hydrocarbon-selective catalytic reactor device. When the space velocity exceeds a predetermined threshold space velocity, a temperature differential across the predetermined forward portion of the hydrocarbon-selective catalytic reactor device is determined, and a threshold temperature as a function of the space velocity and the mass flowrate of the reductant is determined. If the temperature differential across the predetermined forward portion of the hydrocarbon-selective catalytic reactor device is below the threshold temperature, operation of the engine is controlled to regenerate the hydrocarbon-selective catalytic reactor device.

  11. The Nonmethane Hydrocarbon Intercomparison Experiment (NOMHICE): Tasks 1 and 2

    SciTech Connect

    Apel, E.C.; Calvert, J.G.; Fehsenfeld, F.C.

    1994-08-20

    The NOMHICE program has been designed to evaluate current methods being used to determine the ambient levels of various atmospheric nonmethane hydrocarbons, to identify existing problems in these analyses, to correct these problems, and to help ensure quality control of hydrocarbon analyses made by atmospheric scientists throughout the world. To accomplish this, a series of planned experiments (tasks) is now under way which involves all the common classes of the atmospheric hydrocarbons: alkanes, alkenes, alkynes, aromatic hydrocarbons, and the terpenes. The various tasks of the study have been scheduled in order of increasing complexity so that problems can be addressed as they arise. Preliminary results are presented for task 1 and task 2 of a multitask program. Each laboratory used its own analysis and calibration procedures. The first task of NOMHICE involved the circulation of a two-component, gravimetrically prepared, hydrocarbon mixture of known composition and unknown concentration to 36 participating scientific groups from laboratories throughout the world. This experiment was planned to check on the reliability of the standards employed by each of the participating groups. Task 2 involved the circulation, to participant laboratories, of a more complex, gravimetrically prepared, 16-component hydrocarbon mixture (unknown composition and concentration) to determine whether suitable separation, identification, and quantification can be made of the individual hydrocarbons present in the mixture. Further tasks are described which will be carried out in the future. 16 refs., 12 figs., 3 tabs.

  12. The Nonmethane Hydrocarbon Intercomparison Experiment (NOMHICE): Tasks 1 and 2

    NASA Astrophysics Data System (ADS)

    Apel, Eric C.; Calvert, Jack G.; Fehsenfeld, Fred C.

    1994-08-01

    The NOMHICE program has been designed to evaluate current methods being used to determine the ambient levels of various atmospheric nonmethane hydrocarbons, to identify existing problems in these analyses, to correct these problems, and to help ensure quality control of hydrocarbon analyses made by atmospheric scientists throughout the world. To accomplish this, a series of planned experiments (tasks) is now under way which involves all the common classes of the atmospheric hydrocarbons: alkanes, alkenes, alkynes, aromatic hydrocarbons, and the terpenes. The various tasks of the study have been scheduled in order of increasing complexity so that problems can be addressed as they arise. Preliminary results are presented for task 1 and task 2 of a multitask program. Each laboratory used its own analysis and calibration procedures. The first task of NOMHICE involved the circulation of a two-component, gravimetrically prepared, hydrocarbon mixture of known composition and unknown concentration to 36 participating scientific groups from laboratories throughout the world. This experiment was planned to check on the reliability of the standards employed by each of the participating groups. Task 2 involved the circulation, to participant laboratories, of a more complex, gravimetrically prepared, 16-component hydrocarbon mixture (unknown composition and concentration) to determine whether suitable separation, identification, and quantification can be made of the individual hydrocarbons present in the mixture. Further tasks are described which will be carried out in the future.

  13. Methods to assess the amenability of petroleum hydrocarbons to bioremediation.

    PubMed

    Dobson, Richard; Schroth, Martin H; Schuermann, Andreas; Zeyer, Josef

    2004-04-01

    Bioremediation has achieved acceptance as a cost-effective technique for the remediation of soils and groundwater contaminated with petroleum hydrocarbons (PHC). A range of laboratory techniques to assess the biodegradability and bioavailability of PHCs are presented. Biodegradability and bioavailability are important determinants of the bioremediation performance of PHCs. Novel methods for the assessment of the bioavailability of PHC components are described. The techniques are demonstrated for a hydraulic fluid and a spindle oil from a contaminated site. Biodegradation is measured by oxygen consumption and carbon dioxide production. Bioavailability of the PHCs is estimated based on the PHC-water partitioning of tracer compounds and a novel analysis of gas chromatograms based on Raoult's law. The PHCs tested were only partially biodegradable (< 25% in 78 d) due to the low solubility and likely recalcitrance of some of their components. The combination of techniques outlined is expected to be of use in assessing the likely bioremediation performance of PHCs for which published data are scarce or inadequate.

  14. Nonthermal plasma systems and methods for natural gas and heavy hydrocarbon co-conversion

    DOEpatents

    Kong, Peter C.; Nelson, Lee O.; Detering, Brent A.

    2005-05-24

    A reactor for reactive co-conversion of heavy hydrocarbons and hydrocarbon gases and includes a dielectric barrier discharge plasma cell having a pair of electrodes separated by a dielectric material and passageway therebetween. An inlet is provided for feeding heavy hydrocarbons and other reactive materials to the passageway of the discharge plasma cell, and an outlet is provided for discharging reaction products from the reactor. A packed bed catalyst may optionally be used in the reactor to increase efficiency of conversion. The reactor can be modified to allow use of a variety of light sources for providing ultraviolet light within the discharge plasma cell. Methods for upgrading heavy hydrocarbons are also disclosed.

  15. Sample preparation for thermo-gravimetric determination and thermo-gravimetric characterization of refuse derived fuel.

    PubMed

    Robinson, T; Bronson, B; Gogolek, P; Mehrani, P

    2016-02-01

    Thermo-gravimetric analysis (TGA) is a useful method for characterizing fuels. In the past it has been applied to the study of refuse derived fuel (RDF) and related materials. However, the heterogeneity of RDF makes the preparation of small representative samples very difficult and this difficulty has limited the effectiveness of TGA for characterization of RDF. A TGA method was applied to a variety of materials prepared from a commercially available RDF using a variety of procedures. Applicability of TGA method to the determination of the renewable content of RDF was considered. Cryogenic ball milling was found to be an effective means of preparing RDF samples for TGA. When combined with an effective sample preparation, TGA could be used as an alternative method for assessing the renewable content of RDF.

  16. Compounds and methods for the production of long chain hydrocarbons from biological sources

    DOEpatents

    Gordon, John Cameron; Silks, Louis A; Sutton, Andrew D; Wu, Ruilian; Schlaf, Marcel; Waldie, Fraser; West, Ryan; Collias, Dimitris Ioannis

    2016-08-23

    The present invention is directed to the preparation of oxygenated, unsaturated hydrocarbon compounds, such as derivatives of furfural or hydroxymethyl furfural produced by aldol condensation with a ketone or a ketoester, as well as methods of deoxidatively reducing those compounds with hydrogen under acidic conditions to provide saturated hydrocarbons useful as fuels.

  17. Method for producing hydrocarbon fuels from heavy polynuclear hydrocarbons by use of molten metal halide catalyst

    DOEpatents

    Gorin, Everett

    1979-01-01

    In a process for hydrocracking heavy polynuclear carbonaceous feedstocks to produce lighter hydrocarbon fuels by contacting the heavy feedstocks with hydrogen in the presence of a molten metal halide catalyst, thereafter separating at least a substantial portion of the carbonaceous material associated with the reaction mixture from the spent molten metal halide and thereafter regenerating the metal halide catalyst, an improvement comprising contacting the spent molten metal halide catalyst after removal of a major portion of the carbonaceous material therefrom with an additional quantity of hydrogen is disclosed.

  18. Determination of total dietary fiber in selected foods containing resistant maltodextrin by a simplified enzymatic-gravimetric method and liquid chromatography: interlaboratory study in China.

    PubMed

    Fu, Boqiang; Wang, Jing; Roturier, Jean Michel; Tang, Zhiyu; Li, Huan; Wei, Guangyan

    2008-01-01

    An interlaboratory study was conducted in China to validate the modified AOAC Official Method 2001.03 for the determination of total dietary fiber (TDF) in foods containing resistant maltodextrin (RMD), which will be adopted as the National Standard Method of China. The kind of buffer solution, the volume of filtrate evaporation, the volume of eluent for desalting and residual solution after evaporation, etc. were modified, which had been proved to have acceptable accuracy and precision in the routine assay. TDF contents in 3 representative foods and 2 kinds of RMD ingredient (i.e., NUTRIOSE 06 and NUTRIOSE 10) were measured using the modified method in 6 eligible laboratories representing commercial, industrial, and governmental laboratories in China. The results of the interlaboratory study indicated that the intralaboratory repeatability, interlaboratory reproducibility, and precision of the modified method are adequate for reliable analysis of TDF in food containing RMD, as well as resistant dextrin. Compared to AOAC Official Method 2001.03, the modified method is time- and cost-saving.

  19. Method and apparatus for production of subsea hydrocarbon formations

    DOEpatents

    Blandford, J.W.

    1995-01-17

    A system for controlling, separating, processing and exporting well fluids produced from subsea hydrocarbon formations is disclosed. The subsea well tender system includes a surface buoy supporting one or more decks above the water surface for accommodating equipment to process oil, gas and water recovered from the subsea hydrocarbon formation. The surface buoy includes a surface-piercing central flotation column connected to one or more external flotation tanks located below the water surface. The surface buoy is secured to the sea bed by one or more tendons which are anchored to a foundation with piles imbedded in the sea bed. The system accommodates multiple versions on the surface buoy configuration. 20 figures.

  20. Method and apparatus for production of subsea hydrocarbon formations

    DOEpatents

    Blandford, Joseph W.

    1995-01-01

    A system for controlling, separating, processing and exporting well fluids produced from subsea hydrocarbon formations is disclosed. The subsea well tender system includes a surface buoy supporting one or more decks above the water surface for accommodating equipment to process oil, gas and water recovered from the subsea hydrocarbon formation. The surface buoy includes a surface-piercing central flotation column connected to one or more external floatation tanks located below the water surface. The surface buoy is secured to the seabed by one or more tendons which are anchored to a foundation with piles imbedded in the seabed. The system accommodates multiple versions on the surface buoy configuration.

  1. Determination of total dietary fiber in selected foods containing resistant maltodextrin by enzymatic-gravimetric method and liquid chromatography: collaborative study.

    PubMed

    Gordon, Dennis T; Okuma, Kazuhiro

    2002-01-01

    A method was developed for determination of total dietary fiber (TDF) in foods containing resistant maltodextrin (RMD) which includes nondigestible carbohydrates that are not fully recovered as dietary fiber by conventional TDF methods such as AOAC 985.29 or 991.43. Because the average molecular weight (MW) of RMD is 2000 daltons, lower MW soluble dietary fiber components do not precipitate in 78% ethanol; therefore, RMD is not completely quantitated as dietary fiber by current AOAC methods. The accuracy and precision of the method was evaluated through an AOAC collaborative study. Ten laboratories participated and assayed 12 test portions (6 blind duplicates) containing RMD. The 6 test pairs ranged from 1.5 to 100% RMD. The method consisted of the following steps: (1) The insoluble dietary fiber (IDF) and high MW soluble dietary fiber (HMWSDF) were determined by AOAC 985.29. (2) Ion exchange resins were used to remove salts and proteins contained in the AOAC 985.29 filtrates (including ethanol and acetone). (3) The amount of low MWRMD (LMWRMD) in the filtrates were determined by liquid chromatography. (4) The TDF was calculated by summation of the IDF, HMWSDF, and LMWRMD fractions having nondigestible carbohydrates with a degree of polymerization of 3 and higher. Repeatability standard deviations (RSDr) were 1.33-7.46%, calculated by including outliers, and 1.33-6.10%, calculated by not including outliers. Reproducibility standard deviations (RSDR) were 2.48-9.39%, calculated by including outliers, and 1.79-9.39%, calculated by not including outliers. This method is recommended for adoption as Official First Action.

  2. Method for silicon carbide production by reacting silica with hydrocarbon gas

    DOEpatents

    Glatzmaier, Gregory C.

    1994-01-01

    A method is described for producing silicon carbide particles using a silicon source material and a hydrocarbon. The method is efficient and is characterized by high yield. Finely divided silicon source material is contacted with hydrocarbon at a temperature of 400.degree. C. to 1000.degree. C. where the hydrocarbon pyrolyzes and coats the particles with carbon. The particles are then heated to 1100.degree. C. to 1600.degree. C. to cause a reaction between the ingredients to form silicon carbide of very small particle size. No grinding of silicon carbide is required to obtain small particles. The method may be carried out as a batch process or as a continuous process.

  3. Method for silicon carbide production by reacting silica with hydrocarbon gas

    DOEpatents

    Glatzmaier, G.C.

    1994-06-28

    A method is described for producing silicon carbide particles using a silicon source material and a hydrocarbon. The method is efficient and is characterized by high yield. Finely divided silicon source material is contacted with hydrocarbon at a temperature of 400 C to 1000 C where the hydrocarbon pyrolyzes and coats the particles with carbon. The particles are then heated to 1100 C to 1600 C to cause a reaction between the ingredients to form silicon carbide of very small particle size. No grinding of silicon carbide is required to obtain small particles. The method may be carried out as a batch process or as a continuous process. 5 figures.

  4. Apparatus for hydrocarbon extraction

    SciTech Connect

    Bohnert, George W.; Verhulst, Galen G.

    2013-03-19

    Systems and methods for hydrocarbon extraction from hydrocarbon-containing material. Such systems and methods relate to extracting hydrocarbon from hydrocarbon-containing material employing a non-aqueous extractant. Additionally, such systems and methods relate to recovering and reusing non-aqueous extractant employed for extracting hydrocarbon from hydrocarbon-containing material.

  5. Delineation of Hydrocarbon Contamination of Soils and Sediments With Environmental Magnetic Methods: Laboratory and Field Studies

    NASA Astrophysics Data System (ADS)

    Rijal, M. L.; Appel, E.; Porsch, K.; Kappler, A.; Blaha, U.; Petrovsky, E.

    2008-12-01

    Hydrocarbon contamination of soils and sediments is a worldwide environmental problem. The present research focuses on the study of magnetic properties of hydrocarbon contaminated soils and sediments using environmental magnetic methods both on field sites as well as in laboratory batch experiments. The main objectives of this research are i) to determine a possible application of magnetic proxies for the delineation of organic contamination in soils and sediments and ii) to examine the role of bacteria in changing soil magnetic properties after hydrocarbon contamination. A former oil field and a former military site which are heavily contaminated with hydrocarbons were studied. Additionally, three different types of natural clean soils were investigated in laboratory experiments by simulating hydrocarbon contamination in sterile and microbial active setups. Magnetic properties, soil properties, iron bioavailability, iron redox state and hydrocarbon content of samples were measured. Additionally, magnetic susceptibility (MS) was monitored weekly in laboratory batch set-ups during several months. Results from the field sites showed that there is an increase of MS and a good correlation between MS and hydrocarbon content. A weekly monitored MS result from the laboratory study clearly indicated~~10% change (increase as well as decrease) of initial MS of respective soils only in microbial active set-ups with saturation after a few weeks of experimental period. This depicts that there is a change of MS caused by microbial iron mineral transformation in presence of hydrocarbon contamination in soils. The results from the field study demonstrate that magnetic proxies can be used to localize hydrocarbon contamination. However, more field sites with hydrocarbon contaminated soils and sediments need to be investigated by using environmental magnetic methods for better understanding the factors driving such changes in magnetic properties.

  6. COMPUTATIONAL METHODS FOR STUDYING THE INTERACTION BETWEEN POLYCYCLIC AROMATIC HYDROCARBONS AND BIOLOGICAL MACROMOLECULES

    EPA Science Inventory

    Computational Methods for Studying the Interaction between Polycyclic Aromatic Hydrocarbons and Biological Macromolecules .

    The mechanisms for the processes that result in significant biological activity of PAHs depend on the interaction of these molecules or their metabol...

  7. Method for direct conversion of gaseous hydrocarbons to liquids

    DOEpatents

    Kong, Peter C.; Lessing, Paul A.

    2006-03-07

    A chemical reactor for direct conversion of hydrocarbons includes a dielectric barrier discharge plasma cell and a solid oxide electrochemical cell in fluid communication therewith. The discharge plasma cell comprises a pair of electrodes separated by a dielectric material and passageway therebetween. The electrochemical cell comprises a mixed-conducting solid oxide electrolyte membrane tube positioned between a porous cathode and a porous anode, and a gas inlet tube for feeding oxygen containing gas to the porous cathode. An inlet is provided for feeding hydrocarbons to the passageway of the discharge plasma cell, and an outlet is provided for discharging reaction products from the reactor. A packed bed catalyst may optionally be used in the reactor to increase efficiency of conversion. The reactor can be modified to allow use of a light source for directing ultraviolet light into the discharge plasma cell and the electrochemical cell.

  8. Method for removing hydrocarbon contaminants from solid materials

    DOEpatents

    Bala, Gregory A.; Thomas, Charles P.

    1995-01-01

    A system for removing hydrocarbons from solid materials. Contaminated solids are combined with a solvent (preferably terpene based) to produce a mixture. The mixture is washed with water to generate a purified solid product (which is removed from the system) and a drainage product. The drainage product is separated into a first fraction (consisting mostly of contaminated solvent) and a second fraction (containing solids and water). The first fraction is separated into a third fraction (consisting mostly of contaminated solvent) and a fourth fraction (containing residual solids and water). The fourth fraction is combined with the second fraction to produce a sludge which is separated into a fifth fraction (containing water which is ultimately reused) and a sixth fraction (containing solids). The third fraction is then separated into a seventh fraction (consisting of recovered solvent which is ultimately reused) and an eighth fraction (containing hydrocarbon waste).

  9. Method for removing hydrocarbon contaminants from solid materials

    DOEpatents

    Bala, G.A.; Thomas, C.P.

    1995-10-03

    A system is described for removing hydrocarbons from solid materials. Contaminated solids are combined with a solvent (preferably terpene based) to produce a mixture. The mixture is washed with water to generate a purified solid product (which is removed from the system) and a drainage product. The drainage product is separated into a first fraction (consisting mostly of contaminated solvent) and a second fraction (containing solids and water). The first fraction is separated into a third fraction (consisting mostly of contaminated solvent) and a fourth fraction (containing residual solids and water). The fourth fraction is combined with the second fraction to produce a sludge which is separated into a fifth fraction (containing water which is ultimately reused) and a sixth fraction (containing solids). The third fraction is then separated into a seventh fraction (consisting of recovered solvent which is ultimately reused) and an eighth fraction (containing hydrocarbon waste). 4 figs.

  10. Hydrocarbon degradation in soils and methods for soil biotreatment.

    PubMed

    Morgan, P; Watkinson, R J

    1989-01-01

    The cleanup of soils and groundwater contaminated with hydrocarbons is of particular importance in minimizing the environmental impact of petroleum and petroleum products and in preventing contamination of potable water supplies. Consequently, there is a growing industry involved in the treatment of contaminated topsoils, subsoils, and groundwater. The biotreatment methodologies employed for decontamination are designed to enhance in situ degradation by the supply of oxygen, inorganic nutrients, and/or microbial inocula to the contaminated zone. This review considers the fate and effects of hydrocarbon contaminants in terrestrial environments, with particular reference to the factors that limit biodegradation rates. The potential efficiencies, advantages, and disadvantages of biotreatment techniques are discussed and the future research directions necessary for process development are considered.

  11. Method and apparatus for production of subsea hydrocarbon formations

    DOEpatents

    Blandford, Joseph W.

    1992-01-01

    A well tender system for controlling, separating, storing and offloading well fluids produced from subsea hydrocarbon formations. The system comprises a vertically aligned series of tethered cylindrical tanks which are torsionally stabilized by flexible catenary production riser and expert riser bundles, and serviced by separate catenary pipe bundles. Piles are secured to the seabed, each pile assembly being pivotally connected to a lower rigid tendon, which is in turn connected to tendons arranged about the periphery of the interconnected cylindrical tanks.

  12. Method and apparatus for production of subsea hydrocarbon formations

    DOEpatents

    Blandford, Joseph W.

    1994-01-01

    A well tender system for controlling, separating, storing and offloading well fluids produced from subsea hydrocarbon formations. The system comprises a vertically aligned series of tethered cylindrical tanks which are torsionally stabilized by flexible catenary production riser and export riser bundles, and serviced by separate catenary pipe bundles. Piles are secured to the seabed, each pile assembly being pivotally connected to a lower rigid tendon, which is in turn connected to tendons arranged about the periphery of the interconnected cylindrical tanks.

  13. Methods of producing alkylated hydrocarbons from an in situ heat treatment process liquid

    DOEpatents

    Roes, Augustinus Wilhelmus Maria; Mo, Weijian; Muylle, Michel Serge Marie; Mandema, Remco Hugo; Nair, Vijay

    2009-09-01

    A method for producing alkylated hydrocarbons is disclosed. Formation fluid is produced from a subsurface in situ heat treatment process. The formation fluid is separated to produce a liquid stream and a first gas stream. The first gas stream includes olefins. The liquid stream is fractionated to produce at least a second gas stream including hydrocarbons having a carbon number of at least 3. The first gas stream and the second gas stream are introduced into an alkylation unit to produce alkylated hydrocarbons. At least a portion of the olefins in the first gas stream enhance alkylation.

  14. Flow Injection as a Teaching Tool for Gravimetric Analysis

    NASA Astrophysics Data System (ADS)

    Sartini, Raquel P.; Zagatto, Elias A. G.; Oliveira, Cláudio C.

    2000-06-01

    A flow-injection system to carry out gravimetric analysis is presented. Students are faced with an instrumental approach for gravimetric procedures. Crucibles, muffle furnaces, and desiccators are not required. A flowing suspension is established by simultaneously injecting an aqueous sample and a precipitating reagent into two merging carrier streams. The precipitate is accumulated on a minifilter hanging under the plate of an analytical balance and is weighed inside the main stream. Since Archimedes' principle holds, a drying step is not needed. After measurement, the precipitate is dissolved and disposed of. As an application, the determination of phosphate based on precipitation with ammonium and magnesium ions in slightly alkaline medium is chosen. The proposed system is very stable and well suited for demonstration. When applied to analysis of fertilizer extracts with 0.10-1.00% w/v P, it yields precise results (RSD < 0.042) in agreement with an official spectrophotometric method.

  15. A comparative study on hydrocarbon detection using three EMD-based time-frequency analysis methods

    NASA Astrophysics Data System (ADS)

    Xue, Ya-juan; Cao, Jun-xing; Tian, Ren-fei

    2013-02-01

    Due to strong heterogeneity of marine carbonate reservoir, seismic signals become more complex, thus, it is very difficult for hydrocarbon detection. In hydrocarbon reservoir, there usually exist some changes in seismic wave energy and frequency. In their instantaneous spectrums there often exist such phenomena that show the characteristics of attenuation of high frequency energy and enhancement of low-frequency energy. The three EMD-based time-frequency analysis methods' instantaneous spectra all have certain oil and gas detection capability. In this paper, we introduced the Normalized Hilbert Transform (NHT) and a new method named the HU method for hydrocarbon detection. The model results in the Jingbian Gas Field which is located in the eastern Ordos Basin, China, show that NHT and HU methods can be adopted. They also detect the gas-bearing reservoir efficiently as the HHT method does. The three EMD-based methods, that is, the Hilbert-Huang transformation (HHT) and NHT and HU methods, were respectively applied to analyze the seismic data from the Jingbian Gas Field. Firstly, the seismic signals were decomposed into a finite number of intrinsic mode functions (IMFs) by empirical mode decomposition (EMD) method. The second IMF signal (IMF2) of the original seismic section better indicates the distribution of the reservoir. Information on hydrocarbon-bearing reservoir is mainly in IMF2. Secondly, the HHT, NHT and HU methods were respectively used to obtain different frequency division sections from IMF2. Hydrocarbon detection was realized from the energy distribution of the different frequency division sections with these three EMD-based methods. The practical application results show that the three EMD-based methods can all be employed to hydrocarbon detection. Frequency division section of IMF2 using NHT method was better for the seismic data from the Jingbian Gas Field than when using the HHT method and HU method.

  16. Advances on Empirical Mode Decomposition-based Time-Frequency Analysis Methods in Hydrocarbon Detection

    NASA Astrophysics Data System (ADS)

    Chen, H. X.; Xue, Y. J.; Cao, J.

    2015-12-01

    Empirical mode decomposition (EMD), which is a data-driven adaptive decomposition method and is not limited by time-frequency uncertainty spreading, is proved to be more suitable for seismic signals which are nonlinear and non-stationary. Compared with other Fourier-based and wavelet-based time-frequency methods, EMD-based time-frequency methods have higher temporal and spatial resolution and yield hydrocarbon interpretations with more statistical significance. Empirical mode decomposition algorithm has now evolved from EMD to Ensemble EMD (EEMD) to Complete Ensemble EMD (CEEMD). Even though EMD-based time-frequency methods offer many promising features for analyzing and processing geophysical data, there are some limitations or defects in EMD-based time-frequency methods. This presentation will present a comparative study on hydrocarbon detection using seven EMD-based time-frequency analysis methods, which include: (1) first, EMD combined with Hilbert transform (HT) as a time-frequency analysis method is used for hydrocarbon detection; and (2) second, Normalized Hilbert transform (NHT) and HU Methods respectively combined with HT as improved time-frequency analysis methods are applied for hydrocarbon detection; and (3) three, EMD combined with Teager-Kaiser energy (EMD/TK) is investigated for hydrocarbon detection; and (4) four, EMD combined with wavelet transform (EMDWave) as a seismic attenuation estimation method is comparatively studied; and (5) EEMD- and CEEMD- based time-frequency analysis methods used as highlight volumes technology are studied. The differences between these methods in hydrocarbon detection will be discussed. The question of getting a meaningful instantaneous frequency by HT and mode-mixing issues in EMD will be analysed. The work was supported by NSFC under grant Nos. 41430323, 41404102 and 41274128.

  17. Method for determining asphaltene stability of a hydrocarbon-containing material

    DOEpatents

    Schabron, John F; Rovani, Jr., Joseph F

    2013-02-05

    A method for determining asphaltene stability in a hydrocarbon-containing material having solvated asphaltenes therein is disclosed. In at least one embodiment, it involves the steps of: (a) precipitating an amount of the asphaltenes from a liquid sample of the hydrocarbon-containing material with an alkane mobile phase solvent in a column; (b) dissolving a first amount and a second amount of the precipitated asphaltenes by changing the alkane mobile phase solvent to a final mobile phase solvent having a solubility parameter that is higher than the alkane mobile phase solvent; (c) monitoring the concentration of eluted fractions from the column; (d) creating a solubility profile of the dissolved asphaltenes in the hydrocarbon-containing material; and (e) determining one or more asphaltene stability parameters of the hydrocarbon-containing material.

  18. Determination of polycyclic aromatic hydrocarbons in indoor and outdoor air with chromatographic methods.

    PubMed

    Zhu, Li-Zhong; Shen, Xueyou; Liu, Yong-Jian

    2003-05-01

    Polycyclic aromatic hydrocarbons in indoor and outdoor air of four typical homes in Hangzhou, China were determined with a highly automated chromatographic method. The results indicated that the concentrations of the 15 polycyclic aromatic hydrocarbons in the indoor air were between 1.907 microg/m3 and 14.29 microg/m3, which were much higher than those in the corresponding outdoor air. Because of the popular use of mothball in wardrobes, naphthalene had the highest concentration in all the 15 polycyclic aromatic hydrocarbons, which was up to 13.17 microg/m3 and contributed 68% to the total polycyclic aromatic hydrocarbons in the room. In kitchen, because of the representative cooking method, there had much of three- and four-ring polycyclic aromatic hydrocarbons. The indoor smoking not only led to high concentration of polycyclic aromatic hydrocarbons in the indoor air, but also contributed almost all the benzo(a)pyrene. Naphthalene, acenaphthene and pyrene were considered being generated by the indoor sources in all the four homes.

  19. Use of the Complex Conductivity Method to Monitor Hydrocarbon Degradation in Brackish Environments

    NASA Astrophysics Data System (ADS)

    Ntarlagiannis, D.; Beaver, C. L.; Kimak, C.; Slater, L. D.; Atekwana, E. A.; Rossbach, S.

    2015-12-01

    Hydrocarbon contamination of the subsurface is a global environmental problem. The size, location and recurrence rate of contamination very often inhibits active remediation strategies. When there is no direct threat to humans, and direct/invasive remediation methods are prohibited, monitored natural attenuation is often the remediation method of choice. Consequently, long-term monitoring of hydrocarbon degradation is needed to validate remediation. Geophysical methods, frequently utilized to characterize subsurface contamination, have the potential to be adopted for long term monitoring of contaminant degradation. Over the last decade, the complex conductivity method has shown promise as a method for monitoring hydrocarbon degradation processes in freshwater environments. We investigated the sensitivity of complex conductivity to natural attenuation of oil in a brackish setting, being more representative of the conditions where most oil spills occur such as in coastal environments. We performed a series of laboratory hydrocarbon biodegradation experiments whilst continuously monitoring complex conductivity. Sediments from a beach impacted by the Deepwater Horizon (DWH) spill were used to provide the hydrocarbon degraders, while fluids with three different salinities, ranging from fresh water to brackish water, were used as the supporting media. All experimental columns, including two abiotic controls, were run in duplicate. Early results show a dependence of the complex conductivity parameters (both electrolytic and interfacial) on biodegradation processes. Despite the small signals relative to freshwater conditions, the imaginary part of the complex conductivity appears to be sensitive to biodegradation processes. The columns with highest salinity fluids - similar to the salinites for the site where the sediments were collected - showed distinctive complex conductivity responses similar to microbial growth curves. Geochemical monitoring confirmed elevated rates

  20. Gravimetric geoid in the Northwest Pacific Ocean

    NASA Technical Reports Server (NTRS)

    Watts, A. B.; Leeds, A. R.

    1977-01-01

    A total of 3708 1 x 1 deg free-air gravity anomaly averages have been used to construct a new 1 x 1 deg gravimetric geoid of the Northwest Pacific Ocean. The 1 x 1 deg averages are based on a compilation of 147,000 surface ship and pendulum gravity measurements. Difference geoid undulations range from a maximum of +19 m over the Hawaiian ridge to a minimum of -31 m over the junction of the Kuril and Aleutian trenches. The Hawaiian swell is associated with a geoidal high of up to +15 m with wavelengths of about 2200 km and the topographic rises seaward of deep-sea trenches are associated with geoidal highs of up to 4 m with wavelengths of about 220-900 km. The agreement between the gravimetric geoid and Skylab-4 and Geos-3 altimeter data is close for wavelengths greater than about 300 km but poor for shorter wavelengths.

  1. Methods of reforming hydrocarbon fuels using hexaaluminate catalysts

    DOEpatents

    Gardner, Todd H.; Berry, David A.; Shekhawat, Dushyant

    2012-03-27

    A metal substituted hexaaluminate catalyst for reforming hydrocarbon fuels to synthesis gas of the general formula AB.sub.yAl.sub.12-yO.sub.19-.delta., A being selected from alkali metals, alkaline earth metals and lanthanide metals or mixtures thereof. A dopant or surface modifier selected from a transitions metal, a spinel of an oxygen-ion conductor is incorporated. The dopant may be Ca, Cs, K, La, Sr, Ba, Li, Mg, Ce, Co, Fe, Ir, Rh, Ni, Ru, Cu, Pe, Os, Pd, Cr, Mn, W, Re, Sn, Gd, V, Ti, Ag, Au, and mixtures thereof. The oxygen-ion conductor may be a perovskite selected from M'RhO.sub.3, M'PtO.sub.3, M'PdO.sub.3, M'IrO.sub.3, M'RuO.sub.3 wherein M'=Mg, Sr, Ba, La, Ca; a spinel selected from MRh.sub.2O.sub.4, MPt.sub.2O.sub.4, MPd.sub.2O.sub.4, MIr.sub.2O.sub.4, MRu.sub.2O.sub.4 wherein M=Mg, Sr, Ba, La, Ca and mixtures thereof; a florite is selected from M''O.sub.2.

  2. A method of estimating the knock rating of hydrocarbon fuel blend

    NASA Technical Reports Server (NTRS)

    Sanders, Newell D

    1943-01-01

    The usefulness of the knock ratings of pure hydrocarbon compounds would be increased if some reliable method of calculating the knock ratings of fuel blends was known. The purpose of this study was to investigate the possibility of developing a method of predicting the knock ratings of fuel blends.

  3. A Method of Estimating the Knock Rating of Hydrocarbon Fuel Blends

    NASA Technical Reports Server (NTRS)

    Sanders, Newell D.

    1943-01-01

    The usefulness of the knock ratings of pure hydrocarbon compounds would be increased if some reliable method of calculating the knock ratings of fuel blends was known. The purpose of this study was to investigate the possibility of developing a method of predicting the knock ratings of fuel blends.

  4. Estimation of the gravimetric pole tide by stacking long time-series of GGP superconducting gravimeters

    NASA Astrophysics Data System (ADS)

    Ziegler, Yann; Hinderer, Jacques; Rogister, Yves; Rosat, Séverine

    2016-04-01

    We compute the gravimetric factor at the Chandler wobble (CW) frequency using time-series from superconducting gravimeters (SG) longer than a decade. We first individually process the polar motion and data at each individual gravity station to estimate the gravimetric factor amplitude and phase, then we make a global analysis by applying a stacking method to different subsets of up to seven SG stations. The stacking is an efficient way of getting rid of local effects and improving the signal-to-noise ratio of the combined data sets. Using the stacking method, we find a gravimetric factor amplitude and phase of 1.118 ± 0.016 and -0.45 ± 0.66 deg, respectively, which is smaller in amplitude than expected. The sources of error are then carefully considered. For both local and global analyses, the uncertainties on our results are reliably constrained by computing the standard deviation of the estimates of the gravimetric factor amplitude and phase for increasing length of the time-series. Constraints on the CW anelastic dissipation can be set since any departure of the gravimetric factor from its elastic value may provide some insights into the dissipative processes that occur at the CW period. In particular, assuming given rheological models for the Earth's mantle enables us to make the link between the gravimetric factor phase and the CW quality factor.

  5. Method of treating emissions of a hybrid vehicle with a hydrocarbon absorber and a catalyst bypass system

    SciTech Connect

    Roos, Bryan Nathaniel; Gonze, Eugene V; Santoso, Halim G; Spohn, Brian L

    2014-01-14

    A method of treating emissions from an internal combustion engine of a hybrid vehicle includes directing a flow of air created by the internal combustion engine when the internal combustion engine is spinning but not being fueled through a hydrocarbon absorber to collect hydrocarbons within the flow of air. When the hydrocarbon absorber is full and unable to collect additional hydrocarbons, the flow of air is directed through an electrically heated catalyst to treat the flow of air and remove the hydrocarbons. When the hydrocarbon absorber is not full and able to collect additional hydrocarbons, the flow of air is directed through a bypass path that bypasses the electrically heated catalyst to conserve the thermal energy stored within the electrically heated catalyst.

  6. Method for predicting fouling tendency of a hydrocarbon-containing feedstock

    SciTech Connect

    Schabron, John F; Rovani, Jr., Joseph F

    2013-07-23

    Disclosed herein is a method involving the steps of (a) precipitating an amount of asphaltenes from a liquid sample of a first hydrocarbon-containing feedstock having solvated asphaltenes therein with one or more first solvents in a column; (b) determining one or more solubility characteristics of the precipitated asphaltenes; (c) analyzing the one or more solubility characteristics of the precipitated asphaltenes; and (d) correlating a measurement of feedstock fouling tendency for the first hydrocarbon-containing feedstock sample with a mathematical parameter derived from the results of analyzing the one or more solubility characteristics of the precipitated asphaltenes.

  7. Methods of using structures including catalytic materials disposed within porous zeolite materials to synthesize hydrocarbons

    SciTech Connect

    Rollins, Harry W.; Petkovic, Lucia M.; Ginosar, Daniel M.

    2011-02-01

    Catalytic structures include a catalytic material disposed within a zeolite material. The catalytic material may be capable of catalyzing a formation of methanol from carbon monoxide and/or carbon dioxide, and the zeolite material may be capable of catalyzing a formation of hydrocarbon molecules from methanol. The catalytic material may include copper and zinc oxide. The zeolite material may include a first plurality of pores substantially defined by a crystal structure of the zeolite material and a second plurality of pores dispersed throughout the zeolite material. Systems for synthesizing hydrocarbon molecules also include catalytic structures. Methods for synthesizing hydrocarbon molecules include contacting hydrogen and at least one of carbon monoxide and carbon dioxide with such catalytic structures. Catalytic structures are fabricated by forming a zeolite material at least partially around a template structure, removing the template structure, and introducing a catalytic material into the zeolite material.

  8. An interatomic potential for saturated hydrocarbons based on the modified embedded-atom method.

    PubMed

    Nouranian, S; Tschopp, M A; Gwaltney, S R; Baskes, M I; Horstemeyer, M F

    2014-04-01

    In this work, we developed an interatomic potential for saturated hydrocarbons using the modified embedded-atom method (MEAM), a reactive semi-empirical many-body potential based on density functional theory and pair potentials. We parameterized the potential by fitting to a large experimental and first-principles (FP) database consisting of (1) bond distances, bond angles, and atomization energies at 0 K of a homologous series of alkanes and their select isomers from methane to n-octane, (2) the potential energy curves of H2, CH, and C2 diatomics, (3) the potential energy curves of hydrogen, methane, ethane, and propane dimers, i.e., (H2)2, (CH4)2, (C2H6)2, and (C3H8)2, respectively, and (4) pressure-volume-temperature (PVT) data of a dense high-pressure methane system with the density of 0.5534 g cc(-1). We compared the atomization energies and geometries of a range of linear alkanes, cycloalkanes, and free radicals calculated from the MEAM potential to those calculated by other commonly used reactive potentials for hydrocarbons, i.e., second-generation reactive empirical bond order (REBO) and reactive force field (ReaxFF). MEAM reproduced the experimental and/or FP data with accuracy comparable to or better than REBO or ReaxFF. The experimental PVT data for a relatively large series of methane, ethane, propane, and butane systems with different densities were predicted reasonably well by the MEAM potential. Although the MEAM formalism has been applied to atomic systems with predominantly metallic bonding in the past, the current work demonstrates the promising extension of the MEAM potential to covalently bonded molecular systems, specifically saturated hydrocarbons and saturated hydrocarbon-based polymers. The MEAM potential has already been parameterized for a large number of metallic unary, binary, ternary, carbide, nitride, and hydride systems, and extending it to saturated hydrocarbons provides a reliable and transferable potential for atomistic

  9. An interatomic potential for saturated hydrocarbons based on the modified embedded-atom method.

    PubMed

    Nouranian, S; Tschopp, M A; Gwaltney, S R; Baskes, M I; Horstemeyer, M F

    2014-04-01

    In this work, we developed an interatomic potential for saturated hydrocarbons using the modified embedded-atom method (MEAM), a reactive semi-empirical many-body potential based on density functional theory and pair potentials. We parameterized the potential by fitting to a large experimental and first-principles (FP) database consisting of (1) bond distances, bond angles, and atomization energies at 0 K of a homologous series of alkanes and their select isomers from methane to n-octane, (2) the potential energy curves of H2, CH, and C2 diatomics, (3) the potential energy curves of hydrogen, methane, ethane, and propane dimers, i.e., (H2)2, (CH4)2, (C2H6)2, and (C3H8)2, respectively, and (4) pressure-volume-temperature (PVT) data of a dense high-pressure methane system with the density of 0.5534 g cc(-1). We compared the atomization energies and geometries of a range of linear alkanes, cycloalkanes, and free radicals calculated from the MEAM potential to those calculated by other commonly used reactive potentials for hydrocarbons, i.e., second-generation reactive empirical bond order (REBO) and reactive force field (ReaxFF). MEAM reproduced the experimental and/or FP data with accuracy comparable to or better than REBO or ReaxFF. The experimental PVT data for a relatively large series of methane, ethane, propane, and butane systems with different densities were predicted reasonably well by the MEAM potential. Although the MEAM formalism has been applied to atomic systems with predominantly metallic bonding in the past, the current work demonstrates the promising extension of the MEAM potential to covalently bonded molecular systems, specifically saturated hydrocarbons and saturated hydrocarbon-based polymers. The MEAM potential has already been parameterized for a large number of metallic unary, binary, ternary, carbide, nitride, and hydride systems, and extending it to saturated hydrocarbons provides a reliable and transferable potential for atomistic

  10. DNA-based stable isotope probing coupled with cultivation methods implicates Methylophaga in hydrocarbon degradation

    PubMed Central

    Mishamandani, Sara; Gutierrez, Tony; Aitken, Michael D.

    2014-01-01

    Marine hydrocarbon-degrading bacteria perform a fundamental role in the oxidation and ultimate removal of crude oil and its petrochemical derivatives in coastal and open ocean environments. Those with an almost exclusive ability to utilize hydrocarbons as a sole carbon and energy source have been found confined to just a few genera. Here we used stable isotope probing (SIP), a valuable tool to link the phylogeny and function of targeted microbial groups, to investigate hydrocarbon-degrading bacteria in coastal North Carolina sea water (Beaufort Inlet, USA) with uniformly labeled [13C]n-hexadecane. The dominant sequences in clone libraries constructed from 13C-enriched bacterial DNA (from n-hexadecane enrichments) were identified to belong to the genus Alcanivorax, with ≤98% sequence identity to the closest type strain—thus representing a putative novel phylogenetic taxon within this genus. Unexpectedly, we also identified 13C-enriched sequences in heavy DNA fractions that were affiliated to the genus Methylophaga. This is a contentious group since, though some of its members have been proposed to degrade hydrocarbons, substantive evidence has not previously confirmed this. We used quantitative PCR primers targeting the 16S rRNA gene of the SIP-identified Alcanivorax and Methylophaga to determine their abundance in incubations amended with unlabeled n-hexadecane. Both showed substantial increases in gene copy number during the experiments. Subsequently, we isolated a strain representing the SIP-identified Methylophaga sequences (99.9% 16S rRNA gene sequence identity) and used it to show, for the first time, direct evidence of hydrocarbon degradation by a cultured Methylophaga sp. This study demonstrates the value of coupling SIP with cultivation methods to identify and expand on the known diversity of hydrocarbon-degrading bacteria in the marine environment. PMID:24578702

  11. Groundwater storage change detection using micro-gravimetric technology

    NASA Astrophysics Data System (ADS)

    El-Diasty, Mohammed

    2016-06-01

    In this paper, new perspectives and developments in applying a ground-based micro-gravimetric method to detect groundwater storage change in Waterloo Moraine are investigated. Four epochs of gravity survey were conducted using absolute gravimeter (FG5), two relative gravity meters (CG5) and two geodetic global positioning systems (GPS) in the Waterloo Moraine in May and August of 2010 and 2011, respectively. Data were processed using the parametric least-squares method and integrated with geological and hydrological studies. The gravity differences between May and August for 2010 and 2011 epochs were inverted to provide the estimated total water storage changes. Changes in soil water content obtained from land surface models of Ecological Assimilation of Land and Climate Observations (EALCO) and the Global Land Data Assimilation System (GLDAS) program were employed to estimate the groundwater storage change. The ratios between the estimated groundwater storage changes and measured water table changes (specific yields) were determined at a local monitoring well located in the survey area. The results showed that the estimates of specific yields between May and August of 2010 and 2011 were consistent at a significant confidence level and are also within the range of the specific yield from geological and hydrological studies. Therefore, the micro-gravimetric (absolute and relative gravity meters) technology has demonstrated the great potential in detecting groundwater storage change and specific yield for local scale aquifers such as Waterloo Moraine.

  12. ASSESSMENT OF HYDROCARBON SEEPAGE DETECTION METHODS ON THE FORT PECK RESERVATION, NORTHEAST MONTANA

    SciTech Connect

    Lawrence M. Monson

    2003-06-30

    Surface exploration techniques have been employed in separate study areas on the Fort Peck Reservation in northeastern Montana. Anomalies associated with hydrocarbon seepage are documented in all three areas and a variety of surface exploration techniques can be compared. In a small area with established production, Head Gas and Thermal Desorption methods best match production; other methods also map depletion. In a moderate-size area that has prospects defined by 3D seismic data, Head Gas along with Microbial, Iodine, and Eh soil anomalies are all associated with the best hydrocarbon prospect. In a large area that contains many curvilinear patterns observed on Landsat images, that could represent micro-seepage chimneys, results are inconclusive. Reconnaissance mapping using Magnetic Susceptibility has identified a potential prospect; subsequent Soil Gas and Head Gas surveys suggest hydrocarbon potential. In the final year of this project the principle contractor, the Fort Peck Tribes, completed a second survey in the Wicape 3D Seismic Prospect Area (also known as Area 6 in Phase I of the project) and sampled several Landsat image features contained in the Smoke Creek Aeromag Anomaly Area (also known as Area 1 in Phase II of the project). Methods determined to be most useful in Phases I and II, were employed in this final Phase III of the study. The Southwest Wicape seismic anomaly was only partially confirmed. The abundant curvilinears proposed to be possible hydrocarbon micro-seepage chimneys in the Smoke Creek Area were not conclusively verified as such. Insufficient sampling of background data precludes affirmative identification of these mostly topographic Landsat features as gas induced soil and vegetation anomalies. However relatively higher light gas concentrations were found associated with some of the curvilinears. Based on the findings of this work the Assiniboine & Sioux Tribes of the Fort Peck Reservation intend to utilize surface hydrocarbon

  13. Additive Methods for Prediction of Thermochemical Properties. The Laidler Method Revisited. 1. Hydrocarbons

    NASA Astrophysics Data System (ADS)

    Leal, Joa˜O. Paulo

    2006-03-01

    A new parameterization of the Laidler method for estimation of atomization enthalpies and standard enthalpies of formation at 298.15 K for several families of hydrocarbons (alkanes, alkenes, alkynes, polyenes, poly-ynes, alkyl radicals, cycloalkanes, cycloalkenes, benzene derivatives, and polyaromatics) is presented. A total of 200 compounds (164 for liquid phase) are used for the calculation of the parameters. Comparison between the experimental values and those calculated using the group additive scheme led to an average difference of 1.28 kJṡmol-1 for the gas phase enthalpy of formation (excluding the polyaromatic compounds) and of 1.38 kJṡmol-1 for the liquid phase enthalpy of formation. The data base used appears to be essentially error free, but for some compounds (e.g., 2,2,4-trimethyl-pentane, with the highest deviation among all compounds except the polyaromatic ones) the experimental values might need a reevaluation. An Excel worksheet is provided to simplify the calculation of enthalpies of formation and atomization enthalpies based on the Laidler terms defined in this paper.

  14. Long life hydrocarbon conversion catalyst and method of making

    DOEpatents

    Tonkovich, Anna Lee Y [Pasco, WA; Wang, Yong [Richland, WA; Gao, Yufei [Kennewick, WA

    2002-11-12

    The present invention includes a catalyst that has at least four layers, (1) porous support, (2) buffer layer, (3) interfacial layer, and optionally (4) catalyst layer. The buffer layer provides a transition of thermal expansion coefficient from the porous support to the interfacial layer thereby reducing thermal expansion stress as the catalyst is heated to high operating temperatures. The method of the present invention for making the at least three layer catalyst has the steps of (1) selecting a porous support, (2) solution depositing an interfacial layer thereon, and optionally (3) depositing a catalyst material onto the interfacial layer; wherein the improvement comprises (4) depositing a buffer layer between the porous support and the interfacial layer.

  15. In situ respirometry: Field methods and implications for hydrocarbon biodegradation in subsurface soils

    SciTech Connect

    Hickey, W.J.

    1995-07-01

    Using soil ventilation to promote in situ biodegradation is a promising technology for remediation of unsaturated, hydrocarbon-contaminated, subsurface soils. Evaluating in situ hydrocarbon biodegradation rates and levels is a critical part of this approach and determining changes in subsurface O{sub 2} and/or CO{sub 2} levels is a convenient method for monitoring this process because repetitive, noninvasive measurements can be made. In this study, two rapid field procedures for gas analysis, using either liquid- or solid-phase absorption of O{sub 2} and CO{sub 2}, were compared and the implications of these gas measurements for evaluating in situ hydrocarbon biodegradation considered. Air samples were taken from 5 vadose zone piezometers in a gasoline-contaminated soil under treatment by a soil vapor extraction system and one piezometer in a noncontaminated background area. Similar rates and levels of O{sub 2} consumption and CO{sub 2} production were obtained by both techniques during the 20-d study: thus, the method of choice will depend on factors such as cost, air sample volume limitations, or the need for contaminant vapor analyses in the field. While these techniques were good assays for relative microbial activity levels, significant descrepancies between predicted and measured CO{sub 2} levels raised questions concerning the validity of basing hydrocarbon biodegradation estimates solely in O{sub 2} consumption data. To improve the reliability of in situ fuel biodegradation estimates based on O{sub 2} measurements, the relationship(s) between metabolic activities of microbial populations in hydrocarbon-contaminated soils, and changes in subsurface O{sub 2} and CO{sub 2} levels should be clarified. 14 refs., 3 figs., 3 tabs.

  16. Methods of discovery and techniques to study endophytic fungi producing fuel-related hydrocarbons.

    PubMed

    Strobel, Gary A

    2014-01-17

    One promising area in the search for renewable bio-fuels is the discovery of microorganisms that produce fuel-related hydrocarbons (mycodiesel) that is in stark contrast to yeast fermentation that utilizes expensive sugars or starch to produce ethanol, which is a proven and useful source of fuel, but by no means is it ideal. Recently, a number of endophytic fungi have been isolated and described that make compounds such as mono- terpenoids, alkanes, cyclohexanes, cyclopentanes, and alkyl alcohols/ketones, benzenes and polyaromatic hydrocarbons. Many of these compounds are either identical to or are closely related to those specific classes of molecules that are found in diesel. Most importantly, these organisms make hydrocarbons while utilizing cellulosic polymers found in all plant-based agricultural wastes. Also discussed are some novel methods and techniques to quantitatively and qualitatively study hydrocarbon production by these microbes. Two models are discussed for identifying potential fuel-related compounds, scaling up production of them and advanced engine testing. Finally, it seems possible that endophytic fungi may have an additional attribute of having contributed to the formation of crude oil in the first place and a description of the paleobiosphere, to test this hypothesis, is in this review.

  17. Photocatalytic silver enhancement reaction for gravimetric immunosensors

    NASA Astrophysics Data System (ADS)

    Seo, Hyejung; Joo, Jinmyoung; Ko, Wooree; Jung, Namchul; Jeon, Sangmin

    2010-12-01

    A novel microgravimetric immunosensor has been developed using TiO2 nanoparticle-modified immunoassay and silver enhancement reaction. An antibody-conjugated TiO2 nanoparticle is bound to the AFP antigen immobilized on a quartz resonator. When the nanoparticles are exposed to UV light in a silver nitrate solution, the photocatalytic reduction of silver ions results in the formation of metallic silver onto the nanoparticles and induces a decrease in the resonance frequency. The frequency change by this photocatalytic reduction reaction is three orders of magnitude larger than the change by antigen binding alone. The efficiency of the photocatalytic reaction has been found to increase with the fraction of anatase crystallites in the nanoparticles and the concentration of the AgNO3 solution. The results highlight the potential of the photocatalytic nanoparticles for the detection of low concentrations of target molecules using gravimetric sensors.

  18. Photocatalytic silver enhancement reaction for gravimetric immunosensors.

    PubMed

    Seo, Hyejung; Joo, Jinmyoung; Ko, Wooree; Jung, Namchul; Jeon, Sangmin

    2010-12-17

    A novel microgravimetric immunosensor has been developed using TiO(2) nanoparticle-modified immunoassay and silver enhancement reaction. An antibody-conjugated TiO(2) nanoparticle is bound to the AFP antigen immobilized on a quartz resonator. When the nanoparticles are exposed to UV light in a silver nitrate solution, the photocatalytic reduction of silver ions results in the formation of metallic silver onto the nanoparticles and induces a decrease in the resonance frequency. The frequency change by this photocatalytic reduction reaction is three orders of magnitude larger than the change by antigen binding alone. The efficiency of the photocatalytic reaction has been found to increase with the fraction of anatase crystallites in the nanoparticles and the concentration of the AgNO(3) solution. The results highlight the potential of the photocatalytic nanoparticles for the detection of low concentrations of target molecules using gravimetric sensors.

  19. Standardized methods for determination of benz-{alpha}-pyrene in hydrocarbons raw materials and products

    SciTech Connect

    Serkovskaya, G.S.

    1995-11-01

    In this article, the authors will summarize and correlate material on a standard method for the determination of a carcinogenic hydrocarbon - benz-{alpha}-pyrene (BP) - in petroleum crudes and products, and also in products from the processing of peat, coal, shales, and wood. The processing of petroleum, peat, coal, and shales yields exactly the same assortment of products in all cases: gasoline, kerosine, diesel fuel, lube oil, tar, residual fuel oil, heavy resid, pitch, bitumen, wax, paraffin wax, microcrystalline wax, and petrolatum.

  20. Method for simultaneous recovery of hydrogen from water and from hydrocarbons

    DOEpatents

    Willms, R. Scott

    1996-01-01

    Method for simultaneous recovery of hydrogen and hydrogen isotopes from water and from hydrocarbons. A palladium membrane, when utilized in cooperation with a nickel catalyst in a reactor, has been found to drive reactions such as water gas shift, steam reforming and methane cracking to substantial completion by removing the product hydrogen from the reacting mixture. In addition, ultrapure hydrogen is produced, thereby eliminating the need for an additional processing step.

  1. Method for producing hydrocarbon fuels and fuel gas from heavy polynuclear hydrocarbons by the use of molten metal halide catalysts

    DOEpatents

    Gorin, Everett

    1979-01-01

    In a process for hydrocracking heavy polynuclear carbonaceous feedstocks to produce lighter hydrocarbon fuels by contacting the heavy feedstocks with hydrogen in the presence of a molten metal halide catalyst in a hydrocracking zone, thereafter separating at least a major portion of the lighter hydrocarbon fuels from the spent molten metal halide and thereafter regenerating the spent molten metal halide by incinerating the spent molten metal halide by combustion of carbon and sulfur compounds in the spent molten metal halide in an incineration zone, the improvement comprising: (a) contacting the heavy feedstocks and hydrogen in the presence of the molten metal halide in the hydrocracking zone at reaction conditions effective to convert from about 60 to about 90 weight percent of the feedstock to lighter hydrocarbon fuels; (b) separating at least a major portion of the lighter hydrocarbon fuels from the spent molten metal halide; (c) contacting the spent molten metal halide with oxygen in a liquid phase gasification zone at a temperature and pressure sufficient to vaporize from about 25 to about 75 weight percent of the spent metal halide, the oxygen being introduced in an amount sufficient to remove from about 60 to about 90 weight percent of the carbon contained in the spent molten metal halide to produce a fuel gas and regenerated metal halide; and (d) incinerating the spent molten metal halide by combusting carbon and sulfur compounds contained therein.

  2. Q estimation from reflection seismic data for hydrocarbon detection using a modified frequency shift method

    NASA Astrophysics Data System (ADS)

    Li, Fangyu; Zhou, Huailai; Jiang, Nan; Bi, Jianxia; Marfurt, Kurt J.

    2015-08-01

    As a powerfully diagnostic tool for structural interpretation, reservoir characterization, and hydrocarbon detection, quality factor Q provides useful information in seismic processing and interpretation. Popular methods, like the spectral ratio (SR) method, central frequency shift (CFS) method and peak frequency shift (PFS) method, have their respective limitations in dealing with field seismic data. The lack of a reliable method for estimating Q from reflection seismic data is an issue when utilizing the Q value for hydrocarbon detection. In this article, we derive an approximate equation and propose a dominant and central frequency shift (DCFS) method by combining the quality factor Q, the travel time, and dominant and central frequencies of two successive seismic signals along the wave propagating direction. Based on multi-layered analysis, we then proposed a method to obtain continuous volumetric Q estimation results. A test using synthetic data and statistical experiments showed the proposed method can achieve higher accuracy and robustness compared with existing methods. Application of field data also shows its potential and effectiveness to estimate seismic attenuation.

  3. Method for estimating processability of a hydrocarbon-containing feedstock for hydroprocessing

    SciTech Connect

    Schabron, John F; Rovani, Jr., Joseph F

    2014-01-14

    Disclosed herein is a method involving the steps of (a) precipitating an amount of asphaltenes from a liquid sample of a first hydrocarbon-containing feedstock having solvated asphaltenes therein with one or more first solvents in a column; (b) determining one or more solubility characteristics of the precipitated asphaltenes; (c) analyzing the one or more solubility characteristics of the precipitated asphaltenes; and (d) correlating a measurement of feedstock reactivity for the first hydrocarbon-containing feedstock sample with a mathematical parameter derived from the results of analyzing the one or more solubility characteristics of the precipitates asphaltenes. Determined parameters and processabilities for a plurality of feedstocks can be used to generate a mathematical relationship between parameter and processability; this relationship can be used to estimate the processability for hydroprocessing for a feedstock of unknown processability.

  4. Method of upgrading oils containing hydroxyaromatic hydrocarbon compounds to highly aromatic gasoline

    DOEpatents

    Baker, E.G.; Elliott, D.C.

    1993-01-19

    The present invention is a multi-stepped method of converting an oil which is produced by various biomass and coal conversion processes and contains primarily single and multiple ring hydroxyaromatic hydrocarbon compounds to highly aromatic gasoline. The single and multiple ring hydroxyaromatic hydrocarbon compounds in a raw oil material are first deoxygenated to produce a deoxygenated oil material containing single and multiple ring aromatic compounds. Then, water is removed from the deoxygenated oil material. The next step is distillation to remove the single ring aromatic compounds as gasoline. In the third step, the multiple ring aromatics remaining in the deoxygenated oil material are cracked in the presence of hydrogen to produce a cracked oil material containing single ring aromatic compounds. Finally, the cracked oil material is then distilled to remove the single ring aromatics as gasoline.

  5. Method of upgrading oils containing hydroxyaromatic hydrocarbon compounds to highly aromatic gasoline

    DOEpatents

    Baker, Eddie G.; Elliott, Douglas C.

    1993-01-01

    The present invention is a multi-stepped method of converting an oil which is produced by various biomass and coal conversion processes and contains primarily single and multiple ring hydroxyaromatic hydrocarbon compounds to highly aromatic gasoline. The single and multiple ring hydroxyaromatic hydrocarbon compounds in a raw oil material are first deoxygenated to produce a deoxygenated oil material containing single and multiple ring aromatic compounds. Then, water is removed from the deoxygenated oil material. The next step is distillation to remove the single ring aromatic compouns as gasoline. In the third step, the multiple ring aromatics remaining in the deoxygenated oil material are cracked in the presence of hydrogen to produce a cracked oil material containing single ring aromatic compounds. Finally, the cracked oil material is then distilled to remove the single ring aromatics as gasoline.

  6. Polar motion interpretation using gravimetric observations

    NASA Astrophysics Data System (ADS)

    Seoane, L.; Bizouard, C.; Gambis, D.

    2008-04-01

    Polar motion is interpreted as the effect of i) the Earth’s inertia moment changes asso- ciated with the so-called mass term of the Earth’s angular momentum ii) the Earth’s relative angular momentum in the terrestrial frame. Thanks to the GRACE mission and in a lesser extent to LAGEOS missions, the mass term is determined since 2002, independently from any geophysical model. Besides the modeled excitations of the polar motion, i.e the atmospheric angular momentum (AAM), the Oceanic Angular Momentum (OAM), the Hydrological Angular Momentum (HAM), this gravimetric mass term is a new kind of information which can be matched to the observed excitation of the polar motion after removal of the effect of the relative angular momentum, mostly caused by the wind and the oceanic cur- rents. Such comparison, already performed by various authors, is updated for the last releases (RL04) of the gravity field changes i.e. those of the GFZ, CSR, JPL and explored for the mixed LAGEOS-GRACE solution of the GRGS. We confirm that a fair general agreement, especially for the y-component of the equatorial excitation. After removing the modeled oceanic and atmospheric excitations from the signals, we obtain the non-modeled excitation, mostly of hydrological nature; this allows us to compare them to the existing hydrological models, differences might comes from others Earth’s phenomena, for example, earthquakes.

  7. Precision gravimetric survey at the conditions of urban agglomerations

    NASA Astrophysics Data System (ADS)

    Sokolova, Tatiana; Lygin, Ivan; Fadeev, Alexander

    2014-05-01

    Large cities growth and aging lead to the irreversible negative changes of underground. The study of these changes at the urban area mainly based on the shallow methods of Geophysics, which extensive usage restricted by technogenic noise. Among others, precision gravimetry is allocated as method with good resistance to the urban noises. The main the objects of urban gravimetric survey are the soil decompaction, leaded to the rocks strength violation and the karst formation. Their gravity effects are too small, therefore investigation requires the modern high-precision equipment and special methods of measurements. The Gravimetry division of Lomonosov Moscow State University examin of modern precision gravimeters Scintrex CG-5 Autograv since 2006. The main performance characteristics of over 20 precision gravimeters were examined in various operational modes. Stationary mode. Long-term gravimetric measurements were carried at a base station. It shows that records obtained differ by high-frequency and mid-frequency (period 5 - 12 hours) components. The high-frequency component, determined as a standard deviation of measurement, characterizes the level of the system sensitivity to external noise and varies for different devices from 2 to 5-7 μGals. Midrange component, which closely meet to the rest of nonlinearity gravimeter drifts, is partially compensated by the equipment. This factor is very important in the case of gravimetric monitoring or observations, when midrange anomalies are the target ones. For the examined gravimeters, amplitudes' deviations, associated with this parameter may reach 10 μGals. Various transportation modes - were performed by walking (softest mode), lift (vertical overload), vehicle (horizontal overloads), boat (vertical plus horizontal overloads) and helicopter. The survey quality was compared by the variance of the measurement results and internal convergence of series. The measurement results variance (from ±2 to ±4 μGals) and its

  8. The first high-resolution gravimetric geoid for Argentina: GAR

    NASA Astrophysics Data System (ADS)

    Corchete, V.; Pacino, M. C.

    2007-05-01

    This paper describes the new geoid model for Argentina. As only very few geoid solutions are published for South America, any new geoid model could be considered very important. As expected the obtained geoid solution have better accuracy and reliability, than the global EIGEN-GL04C model, which was derived recently with the most advanced techniques and the best database available up to 2006. The computation method was the Stokes integral in convolution form, which is proved as an efficient tool to reach the expected objective. The terrain corrections have been computed from a digital terrain model based on the SRTM (Shuttler Radar Topography Mission) 90M database. These corrections were used to obtain the residual anomalies from the gridded gravity anomalies. The indirect effect has been also taken into account. The new geoid model is obtained on a regular 1.5' × 1.5' grid in the GRS80 reference system, covering Argentina and the surrounding area, from -56° to -21° of latitude and from -75° to -53° of longitude. This gravimetric geoid and the EIGEN-GL04C model are compared to geoid undulations derived at 393 GPS/levelling points, located at the study area. As it is expected, the new geoid shows a better fit at the 393 validation points than the global geoid model. The new gravimetric geoid solution could be very important for engineering purposes to provide an improved reference surface may be used in connection with GPS measurements and altimetric observations, as well as for geophysical purposes.

  9. Description of heat flux measurement methods used in hydrocarbon and propellant fuel fires at Sandia.

    SciTech Connect

    Nakos, James Thomas

    2010-12-01

    The purpose of this report is to describe the methods commonly used to measure heat flux in fire applications at Sandia National Laboratories in both hydrocarbon (JP-8 jet fuel, diesel fuel, etc.) and propellant fires. Because these environments are very severe, many commercially available heat flux gauges do not survive the test, so alternative methods had to be developed. Specially built sensors include 'calorimeters' that use a temperature measurement to infer heat flux by use of a model (heat balance on the sensing surface) or by using an inverse heat conduction method. These specialty-built sensors are made rugged so they will survive the environment, so are not optimally designed for ease of use or accuracy. Other methods include radiometers, co-axial thermocouples, directional flame thermometers (DFTs), Sandia 'heat flux gauges', transpiration radiometers, and transverse Seebeck coefficient heat flux gauges. Typical applications are described and pros and cons of each method are listed.

  10. Reaction Mechanism of Oxygen Atoms with Unsaturated Hydrocarbons by the Crossed-Molecular-Beams Method

    DOE R&D Accomplishments Database

    Buss, R. J.; Baseman, R. J.; Guozhong, H.; Lee, Y. T.

    1982-04-01

    From a series of studies of the reaction of oxygen atoms with unsaturated hydrocarbons using the crossed molecular beam method, the dominant reaction mechanisms were found to be the simple substitution reactions with oxygen atoms replacing H, Cl, Br atom or alkyl groups. Complication due to secondary reaction was avoided by carrying out experiments under single collisions and observing primary products directly. Primary products were identified by measuring the angular and velocity distributions of products at all the mass numbers which could be detected by the mass spectrometer, and from comparison of these distributions, applying the requirement of energy and momentum conservation.

  11. A simple method for calculating growth rates of petroleum hydrocarbon plumes

    USGS Publications Warehouse

    Bekins, B.A.; Cozzarelli, I.M.; Curtis, G.P.

    2005-01-01

    Consumption of aquifer Fe(III) during biodegradation of ground water contaminants may result in expansion of a contaminant plume, changing the outlook for monitored natural attenuation. Data from two research sites contaminated with petroleum hydrocarbons show that toluene and xylenes degrade under methanogenic conditions, but the benzene and ethylbenzene plumes grow as aquifer Fe(III) supplies are depleted. By considering a one-dimensional reaction front in a constant unidirectional flow field, it is possible to derive a simple expression for the growth rate of a benzene plume. The method balances the mass flux of benzene with the Fe(III) content of the aquifer, assuming that the biodegradation reaction is instantaneous. The resulting expression shows that the benzene front migration is retarded relative to the ground water velocity by a factor that depends on the concentrations of hydrocarbon and bioavailable Fe(III). The method provides good agreement with benzene plumes at a crude oil study site in Minnesota and a gasoline site in South Carolina. Compared to the South Carolina site, the Minnesota site has 25% higher benzene flux but eight times the Fe(III), leading to about one-sixth the expansion rate. Although it was developed for benzene, toluene, ethylbenzene, and xylenes, the growth-rate estimation method may have applications to contaminant plumes from other persistent contaminant sources. Copyright ?? 2005 National Ground Water Association.

  12. Comparison of gravimetric and spectroscopic approaches to quantify stratum corneum removed by tape-stripping.

    PubMed

    Mohammed, D; Yang, Q; Guy, R H; Matts, P J; Hadgraft, J; Lane, M E

    2012-09-01

    Skin surface tape-stripping is an extensively used technique to examine the distribution profile, penetration and safety of various active compounds. It is also a widely accepted method to probe skin barrier properties and more specifically, those of the stratum corneum (SC). The amount of SC removed by tape-stripping is generally determined either gravimetrically or by extraction and measurement of SC proteins. A novel infra-red densitometry (IRD) technique has recently been introduced to measure SC protein content. In the present study, IRD was investigated as an alternative method to measure the mass of SC removed by tape-stripping. Tape-stripping experiments were conducted on human volunteers. The weight of the stratum corneum removed was assessed by the gravimetric approach and by IRD. Transepidermal water loss (TEWL) was also measured before and after each tape-strip. A linear correlation coefficient was obtained for the data from the gravimetric and IRD measurements (r(2)=0.65; n=240). IRD is therefore proposed as a rapid, non-destructive alternative to the gravimetric approach to estimate the amount of SC removed by tape-stripping in vivo. PMID:22713518

  13. Comparison of gravimetric and spectroscopic approaches to quantify stratum corneum removed by tape-stripping.

    PubMed

    Mohammed, D; Yang, Q; Guy, R H; Matts, P J; Hadgraft, J; Lane, M E

    2012-09-01

    Skin surface tape-stripping is an extensively used technique to examine the distribution profile, penetration and safety of various active compounds. It is also a widely accepted method to probe skin barrier properties and more specifically, those of the stratum corneum (SC). The amount of SC removed by tape-stripping is generally determined either gravimetrically or by extraction and measurement of SC proteins. A novel infra-red densitometry (IRD) technique has recently been introduced to measure SC protein content. In the present study, IRD was investigated as an alternative method to measure the mass of SC removed by tape-stripping. Tape-stripping experiments were conducted on human volunteers. The weight of the stratum corneum removed was assessed by the gravimetric approach and by IRD. Transepidermal water loss (TEWL) was also measured before and after each tape-strip. A linear correlation coefficient was obtained for the data from the gravimetric and IRD measurements (r(2)=0.65; n=240). IRD is therefore proposed as a rapid, non-destructive alternative to the gravimetric approach to estimate the amount of SC removed by tape-stripping in vivo.

  14. Does mode mixing matter in EMD-based highlight volume methods for hydrocarbon detection? Experimental evidence

    NASA Astrophysics Data System (ADS)

    Xue, Ya-juan; Cao, Jun-xing; Du, Hao-kun; Zhang, Gu-lan; Yao, Yao

    2016-09-01

    Empirical mode decomposition (EMD)-based spectral decomposition methods have been successfully used for hydrocarbon detection. However, mode mixing that occurs during the sifting process of EMD causes the 'true' intrinsic mode function (IMF) to be extracted incorrectly and blurs the physical meaning of the IMF. We address the issue of how the mode mixing influences the EMD-based methods for hydrocarbon detection by introducing mode-mixing elimination methods, specifically ensemble EMD (EEMD) and complete ensemble EMD (CEEMD)-based highlight volumes, as feasible tools that can identify the peak amplitude above average volume and the peak frequency volume. Three schemes, that is, using all IMFs, selected IMFs or weighted IMFs, are employed in the EMD-, EEMD- and CEEMD-based highlight volume methods. When these methods were applied to seismic data from a tight sandstone gas field in Central Sichuan, China, the results demonstrated that the amplitude anomaly in the peak amplitude above average volume captured by EMD, EEMD and CEEMD combined with Hilbert transforms, whether using all IMFs, selected IMFs or weighted IMFs, are almost identical to each other. However, clear distinctions can be found in the peak frequency volume when comparing results generated using all IMFs, selected IMFs, or weighted IMFs. If all IMFs are used, the influence of mode mixing on the peak frequency volume is not readily discernable. However, using selected IMFs or a weighted IMFs' scheme affects the peak frequency in relation to the reservoir thickness in the EMD-based method. Significant improvement in the peak frequency volume can be achieved in EEMD-based highlight volumes using selected IMFs. However, if the weighted IMFs' scheme is adopted (i.e., if the undesired IMFs are included with reduced weights rather than excluded from the analysis entirely), the CEEMD-based peak frequency volume provides a more accurate reservoir thickness estimate compared with the other two methods. This

  15. Culture-Dependent and -Independent Methods Capture Different Microbial Community Fractions in Hydrocarbon-Contaminated Soils

    PubMed Central

    Stefani, Franck O. P.; Bell, Terrence H.; Marchand, Charlotte; de la Providencia, Ivan E.; El Yassimi, Abdel; St-Arnaud, Marc; Hijri, Mohamed

    2015-01-01

    Bioremediation is a cost-effective and sustainable approach for treating polluted soils, but our ability to improve on current bioremediation strategies depends on our ability to isolate microorganisms from these soils. Although culturing is widely used in bioremediation research and applications, it is unknown whether the composition of cultured isolates closely mirrors the indigenous microbial community from contaminated soils. To assess this, we paired culture-independent (454-pyrosequencing of total soil DNA) with culture-dependent (isolation using seven different growth media) techniques to analyse the bacterial and fungal communities from hydrocarbon-contaminated soils. Although bacterial and fungal rarefaction curves were saturated for both methods, only 2.4% and 8.2% of the bacterial and fungal OTUs, respectively, were shared between datasets. Isolated taxa increased the total recovered species richness by only 2% for bacteria and 5% for fungi. Interestingly, none of the bacteria that we isolated were representative of the major bacterial OTUs recovered by 454-pyrosequencing. Isolation of fungi was moderately more effective at capturing the dominant OTUs observed by culture-independent analysis, as 3 of 31 cultured fungal strains ranked among the 20 most abundant fungal OTUs in the 454-pyrosequencing dataset. This study is one of the most comprehensive comparisons of microbial communities from hydrocarbon-contaminated soils using both isolation and high-throughput sequencing methods. PMID:26053848

  16. Gravimetric Determination of Calcium as Calcium Carbonate Hydrate.

    ERIC Educational Resources Information Center

    Henrickson, Charles H.; Robinson, Paul R.

    1979-01-01

    The gravimetric determination of calcium as calcium carbonate is described. This experiment is suitable for undergraduate quantitative analysis laboratories. It is less expensive than determination of chloride as silver chloride. (BB)

  17. Application of random forests method to predict the retention indices of some polycyclic aromatic hydrocarbons.

    PubMed

    Goudarzi, N; Shahsavani, D; Emadi-Gandaghi, F; Chamjangali, M Arab

    2014-03-14

    In this work, a quantitative structure-retention relationship (QSRR) investigation was carried out based on the new method of random forests (RF) for prediction of the retention indices (RIs) of some polycyclic aromatic hydrocarbon (PAH) compounds. The RIs of these compounds were calculated using the theoretical descriptors generated from their molecular structures. Effects of the important parameters affecting the ability of the RF prediction power such as the number of trees (nt) and the number of randomly selected variables to split each node (m) were investigated. Optimization of these parameters showed that in the point m=70, nt=460, the RF method can give the best results. Also, performance of the RF model was compared with that of the artificial neural network (ANN) and multiple linear regression (MLR) techniques. The results obtained show the relative superiority of the RF method over the MLR and ANN ones.

  18. Field studies: Test method for on-line continuous measurement of total hydrocarbons (THC) and non-methane hydrocarbons (NMHC) in stack gas

    SciTech Connect

    Hsiao, H.H.; Lai, C.C.; Chu, H.W.; Cheng, H.

    1999-07-01

    A new method for on-line monitoring of total hydrocarbons and non-methane hydrocarbons in stack gas simultaneously was developed in this study. Based on the principle of on-line GC/FID, the method was developed and can be considered as a new modification of the Method 25 and 25A of US EPA. Major advantages of the method included (1) capability of distinguishing methane as Method 25; (2) near-real-time results; (3) broad species coverage; (4) monitoring methane in straightforward manner; (5) low operation and maintenance costs. In the proposed method, test samples were continuously pumped from detection sources and loaded with a two-loop sampling valve. The samples were then injected into two GC columns-empty and molecular sieve columns. The empty column was used for detection of THC, and the molecular sieve column was for methane. The detector in this GC was FID. NMHC concentration was obtained by subtracting methane from THC. The tests were carried out to measure the THC and methane in waste gas in various industries, including surface coating, semiconductor manufacturing, synthetic leather industries. Recovery rates of THC in the samples were between 86% to 114% for about 100 m of transfer line of samples. For the standard gas, the recovery rate was about 101%, 6.6 % of measurement precision, and 88%--114% of accuracy. The results showed the promising and reliable measurement of the test method for THC and methane in waste gas.

  19. Method for producing low-cost, high volume hydrogen from hydrocarbon sources

    SciTech Connect

    Bose, Arun C.; Balachandran, Uthamalinga; Kleerfisch, Mark S.; Udovich, Carl A.; Stiegel, Gary J.

    1997-12-01

    A method is described for the conversion of naturally-occurring or biomass-derived lower to higher hydrocarbon (C{sub x}H{sub y},where x may vary from 1--3 and y may vary from 4--8) to low-cost, high-volume hydrogen. In one embodiment, methane, the major component of natural gas, is reacted in a single reaction zone of a mixed-conducting ceramic membrane reactor to form hydrogen via simultaneous partial oxidation and water gas shift reactions at temperatures required for thermal excitations of the mixed-conducting membranes. The hydrogen is produced by catalytically reacting the hydrocarbon with oxygen to form synthesis gas (a mixture of carbon monoxide and hydrogen), followed by a water gas shift (WGS) reaction with steam, wherein both reactions occur in a single reaction zone having a multi-functional catalyst or a combination of catalysts. The hydrogen is separated from other reaction products by membrane-assisted transport or by pressure-swing adsorption technique. Membrane-assisted transport may occur via proton transfer or molecular sieving mechanisms.

  20. "Density equilibrium" method for the quantitative and rapid in situ determination of lipid, hydrocarbon, or biopolymer content in microorganisms.

    PubMed

    Eroglu, Ela; Melis, Anastasios

    2009-04-01

    The work provides a simple method, based on a direct density equilibrium measurement, for the rapid in situ estimation of total lipid, hydrocarbon or biopolymer content in a variety of prokaryotic and eukaryotic samples. The method can be readily applied to live microalgae and photosynthetic bacteria, single-celled or colonial microorganisms, as well as cellular fractions and isolated subcellular compartments or components. In this approach, the absolute lipid, hydrocarbon, or biopolymer content of the cells can be readily calculated. This method is especially useful for tracking the oil or polymer content of strains of microalgae and other microorganisms, whose lipid, hydrocarbon or biopolymer content may change with cultivation conditions and/or time, as the case would be in microorganism lipid-induction industrial processes. The method is also useful for the direct in situ measurement of storage polymer accumulation in live cells, such as starch in microalgae and polyhydroxybutyrate, or other polyhydroxyalkanoates, in photosynthetic and non-photosynthetic bacteria. PMID:19031427

  1. Systems and methods for optically measuring properties of hydrocarbon fuel gases

    DOEpatents

    Adler-Golden, S.; Bernstein, L.S.; Bien, F.; Gersh, M.E.; Goldstein, N.

    1998-10-13

    A system and method for optical interrogation and measurement of a hydrocarbon fuel gas includes a light source generating light at near-visible wavelengths. A cell containing the gas is optically coupled to the light source which is in turn partially transmitted by the sample. A spectrometer disperses the transmitted light and captures an image thereof. The image is captured by a low-cost silicon-based two-dimensional CCD array. The captured spectral image is processed by electronics for determining energy or BTU content and composition of the gas. The innovative optical approach provides a relatively inexpensive, durable, maintenance-free sensor and method which is reliable in the field and relatively simple to calibrate. In view of the above, accurate monitoring is possible at a plurality of locations along the distribution chain leading to more efficient distribution. 14 figs.

  2. Systems and methods for optically measuring properties of hydrocarbon fuel gases

    DOEpatents

    Adler-Golden, Steven; Bernstein, Lawrence S.; Bien, Fritz; Gersh, Michael E.; Goldstein, Neil

    1998-10-13

    A system and method for optical interrogation and measurement of a hydrocarbon fuel gas includes a light source generating light at near-visible wavelengths. A cell containing the gas is optically coupled to the light source which is in turn partially transmitted by the sample. A spectrometer disperses the transmitted light and captures an image thereof. The image is captured by a low-cost silicon-based two-dimensional CCD array. The captured spectral image is processed by electronics for determining energy or BTU content and composition of the gas. The innovative optical approach provides a relatively inexpensive, durable, maintenance-free sensor and method which is reliable in the field and relatively simple to calibrate. In view of the above, accurate monitoring is possible at a plurality of locations along the distribution chain leading to more efficient distribution.

  3. Interpretation of Gravimetric and Aeromagnetic Data of the Tecoripa Chart in Southeast Sonora, Mexico.

    NASA Astrophysics Data System (ADS)

    Martínez-Retama, S.; Montaño-Del Cid, M. A.

    2015-12-01

    The Tecoripa chart H12-D64 is located southeast of the state of Sonora, México, south of Arizona. The geology is represented by sedimentary rocks of the Ordovician and Triassic, volcanic rocks of the Upper Cretaceous and Tertiary, intrusive rocks from the Upper Cretaceous- Tertiary and sedimentary rocks of the Cenozoic. In this paper a gravimetric study was conducted to determine the configuration and depth of the basement and to develop a structural model of the subsurface. For this purpose a consistent gravimetric survey in 3 profiles was conducted. To complement this study, gravimetric data obtained by INEGI (96 gravimetric stations spaced every 4000 m) that correspond to a regional survey was also used. The two sets of data were corrected and processed with the WinGLink software. The profiles were then modeled using the Talwani method. 4 Profiles corresponding to the gravimetric survey and 5 data profiles from INEGI were modeled. Aeromagnetic data from the total field of Tecoripa chart were also processed. The digital information was integrated and processed by generating a data grid. Processes applied to data consisted of reduction to the pole, regional-residual separation and upward continuations. In general, the obtained structural models show intrusive bodies associated with well-defined high gravimetric and magnetic and low gravimetric and magnetic are associated with basins and sedimentary rocks. The obtained geological models show the basement represented by volcanic rocks of the Tarahumara Formation from the Upper Cretaceous which are in contact with sedimentary rocks from the Barranca Group from Upper Cretaceous and limestones from the Middle Ordovician. Both volcanic and sedimentary rocks are intruded by granodiorite- granite with ages of the Tertiary-Oligocene. Based on the superficial geology as well as in the configuration of the basement and the obtained structural model the existence of faults with NW-SE orientation that originate Horst and

  4. Development of an Efficient Bacterial Consortium for the Potential Remediation of Hydrocarbons from Contaminated Sites

    PubMed Central

    Patowary, Kaustuvmani; Patowary, Rupshikha; Kalita, Mohan C.; Deka, Suresh

    2016-01-01

    The intrinsic biodegradability of hydrocarbons and the distribution of proficient degrading microorganisms in the environment are very crucial for the implementation of bioremediation practices. Among others, one of the most favorable methods that can enhance the effectiveness of bioremediation of hydrocarbon-contaminated environment is the application of biosurfactant producing microbes. In the present study, the biodegradation capacities of native bacterial consortia toward total petroleum hydrocarbons (TPH) with special emphasis to poly aromatic hydrocarbons were determined. The purpose of the study was to isolate TPH degrading bacterial strains from various petroleum contaminated soil of Assam, India and develop a robust bacterial consortium for bioremediation of crude oil of this native land. From a total of 23 bacterial isolates obtained from three different hydrocarbons contaminated samples five isolates, namely KS2, PG1, PG5, R1, and R2 were selected as efficient crude oil degraders with respect to their growth on crude oil enriched samples. Isolates KS2, PG1, and R2 are biosurfactant producers and PG5, R1 are non-producers. Fourteen different consortia were designed involving both biosurfactant producing and non-producing isolates. Consortium 10, which comprises two Bacillus strains namely, Bacillus pumilus KS2 and B. cereus R2 (identified by 16s rRNA sequencing) has shown the best result in the desired degradation of crude oil. The consortium showed degradation up to 84.15% of TPH after 5 weeks of incubation, as revealed from gravimetric analysis. FTIR (Fourier transform infrared) and GCMS (Gas chromatography-mass spectrometer) analyses were correlated with gravimetric data which reveals that the consortium has removed a wide range of petroleum hydrocarbons in comparison with abiotic control including different aliphatic and aromatic hydrocarbons. PMID:27471499

  5. Development of an Efficient Bacterial Consortium for the Potential Remediation of Hydrocarbons from Contaminated Sites.

    PubMed

    Patowary, Kaustuvmani; Patowary, Rupshikha; Kalita, Mohan C; Deka, Suresh

    2016-01-01

    The intrinsic biodegradability of hydrocarbons and the distribution of proficient degrading microorganisms in the environment are very crucial for the implementation of bioremediation practices. Among others, one of the most favorable methods that can enhance the effectiveness of bioremediation of hydrocarbon-contaminated environment is the application of biosurfactant producing microbes. In the present study, the biodegradation capacities of native bacterial consortia toward total petroleum hydrocarbons (TPH) with special emphasis to poly aromatic hydrocarbons were determined. The purpose of the study was to isolate TPH degrading bacterial strains from various petroleum contaminated soil of Assam, India and develop a robust bacterial consortium for bioremediation of crude oil of this native land. From a total of 23 bacterial isolates obtained from three different hydrocarbons contaminated samples five isolates, namely KS2, PG1, PG5, R1, and R2 were selected as efficient crude oil degraders with respect to their growth on crude oil enriched samples. Isolates KS2, PG1, and R2 are biosurfactant producers and PG5, R1 are non-producers. Fourteen different consortia were designed involving both biosurfactant producing and non-producing isolates. Consortium 10, which comprises two Bacillus strains namely, Bacillus pumilus KS2 and B. cereus R2 (identified by 16s rRNA sequencing) has shown the best result in the desired degradation of crude oil. The consortium showed degradation up to 84.15% of TPH after 5 weeks of incubation, as revealed from gravimetric analysis. FTIR (Fourier transform infrared) and GCMS (Gas chromatography-mass spectrometer) analyses were correlated with gravimetric data which reveals that the consortium has removed a wide range of petroleum hydrocarbons in comparison with abiotic control including different aliphatic and aromatic hydrocarbons.

  6. Development of an Efficient Bacterial Consortium for the Potential Remediation of Hydrocarbons from Contaminated Sites.

    PubMed

    Patowary, Kaustuvmani; Patowary, Rupshikha; Kalita, Mohan C; Deka, Suresh

    2016-01-01

    The intrinsic biodegradability of hydrocarbons and the distribution of proficient degrading microorganisms in the environment are very crucial for the implementation of bioremediation practices. Among others, one of the most favorable methods that can enhance the effectiveness of bioremediation of hydrocarbon-contaminated environment is the application of biosurfactant producing microbes. In the present study, the biodegradation capacities of native bacterial consortia toward total petroleum hydrocarbons (TPH) with special emphasis to poly aromatic hydrocarbons were determined. The purpose of the study was to isolate TPH degrading bacterial strains from various petroleum contaminated soil of Assam, India and develop a robust bacterial consortium for bioremediation of crude oil of this native land. From a total of 23 bacterial isolates obtained from three different hydrocarbons contaminated samples five isolates, namely KS2, PG1, PG5, R1, and R2 were selected as efficient crude oil degraders with respect to their growth on crude oil enriched samples. Isolates KS2, PG1, and R2 are biosurfactant producers and PG5, R1 are non-producers. Fourteen different consortia were designed involving both biosurfactant producing and non-producing isolates. Consortium 10, which comprises two Bacillus strains namely, Bacillus pumilus KS2 and B. cereus R2 (identified by 16s rRNA sequencing) has shown the best result in the desired degradation of crude oil. The consortium showed degradation up to 84.15% of TPH after 5 weeks of incubation, as revealed from gravimetric analysis. FTIR (Fourier transform infrared) and GCMS (Gas chromatography-mass spectrometer) analyses were correlated with gravimetric data which reveals that the consortium has removed a wide range of petroleum hydrocarbons in comparison with abiotic control including different aliphatic and aromatic hydrocarbons. PMID:27471499

  7. Hydrocarbon product stripping

    SciTech Connect

    Harandi, M.N.; Owen, H.; Siuta, M.T.

    1989-04-18

    A method is described for stripping light gasiform components from the liquid effluent of a catalytic hydrodesulfurization process, which comprises separating the liquid effluent containing relatively low boiling hydrocarbon components, relatively high boiling hydrocarbon components, hydrogen, and hydrogen sulfide.

  8. Fourier transform infrared method validation at a carbon bed solvent recovery unit for four gaseous hydrocarbons

    SciTech Connect

    Reagen, W.K.; Wright, B.D.; Krueger, D.J.; Plummer, G.M.

    1999-05-15

    The authors report the results of a 1995 study in which Fourier transform infrared (FTIR) gas-phase spectrometry was employed to measure the concentrations of four organic compounds (tetrahydrofuran, toluene, 2-butanone, and cyclohexanone) in the gas stream of an industrial solvent recovery unit. The goals of the study were to demonstrate that the extractive FTIR technique is (1) suitable for compliance measurements of the four individual compound concentrations and (2) an accurate substitute for flame ionization detection determinations of the total hydrocarbon content of the gas stream. The US Environmental Protection Agency (EPA) provides guidance on this type of study in its Method 301, which lists specific procedures and statistical criteria, and in several recently published documents describing FTIR quality assurance/quality control measures. The EPA reviews of the procedures and results indicate that both goals of the study were met according to EPA standards.

  9. Hydrocarbon pneumonia

    MedlinePlus

    Pneumonia - hydrocarbon ... Coughing Fever Shortness of breath Smell of a hydrocarbon product on the breath Stupor (decreased level of ... Most children who drink or inhale hydrocarbon products and develop ... hydrocarbons may lead to rapid respiratory failure and death.

  10. Method of preparing and utilizing a catalyst system for an oxidation process on a gaseous hydrocarbon stream

    DOEpatents

    Berry, David A; Shekhawat, Dushyant; Smith, Mark; Haynes, Daniel

    2013-07-16

    The disclosure relates to a method of utilizing a catalyst system for an oxidation process on a gaseous hydrocarbon stream with a mitigation of carbon accumulation. The system is comprised of a catalytically active phase deposited onto an oxygen conducting phase, with or without supplemental support. The catalytically active phase has a specified crystal structure where at least one catalytically active metal is a cation within the crystal structure and coordinated with oxygen atoms within the crystal structure. The catalyst system employs an optimum coverage ratio for a given set of oxidation conditions, based on a specified hydrocarbon conversion and a carbon deposition limit. Specific embodiments of the catalyst system are disclosed.

  11. Reclamation and reuse of freon in total petroleum hydrocarbon analyses

    SciTech Connect

    Ekechukwu, A.A.; Peterson, S.F.

    1996-04-01

    ADS is using a commercially available solvent reclamation system to recycle 95-97 percent of the Freon used in total petroleum hydrocarbon analyses. ADS has further developed the commercially available solvent reclamation system to accommodate radioactive contaminated Freon. This report establishes the following: validity of the method; success of recycling; and effect of radionuclides in recycling radioactive contaminated Freon. The standard analysis method for determining total petroleum hydrocarbons (commonly known as oil and grease determination) involves solvent extraction of the hydrocarbons using Freon followed by quantitation using infrared detection. This has been the method of choice because it is simple, rugged, inexpensive, and applicable to both solid and liquid samples and to radioactive samples. Due to its deleterious effect on the ozone layer, the use of Freon and other chloro-fluorocarbons (CFCs) has been greatly restricted. Freon has become very expensive (800$/liter) and will soon be unavailable entirely. Several methods have been proposed to replace the Freon extraction method. These methods include solid-phase extraction, solvent extraction, and supercritical fluid extraction all of which use gravimetric determination or infrared analysis of the extracted hydrocarbons. These methods are not as precise or as sensitive as the Freon extraction method, and a larger amount of sample is therefore required due to the decreased sensitivity. The solid phase extraction method cannot accommodate solid samples. Supercritical fluid extraction requires expensive instrumentation. ADS opted to keep the existing Freon method and recycle the solvent. An inexpensive solvent reclamation system was procured to reclaim the spent Freon. This reclaimer removes hydrocarbons from the Freon solvent by passage through an activated carbon bed.

  12. Standard test method for heat of combustion of hydrocarbon fuels by bomb calorimeter (high-precision method)

    SciTech Connect

    Not Available

    1980-01-01

    This method covers the determination of the heat of combustion of hydrocarbon fuels. It is designed specifically for use with aviation turbine fuels when the permissible difference between duplicate determinations is of the order of 0.1%. It can be used for a wide range of volatile and nonvolatile materials where slightly greater differences in precision can be tolerated. The heat of combustion is determined by burning a weighed sample in an oxygen-bomb calorimeter under controlled conditions. The temperature is measured by means of a platinum resistance thermometer. The heat of combustion is calculated from temperature observations before, during, and after combustion, with proper allowance for thermochemical and heat-transfer corrections. Either isothermal or adiabatic calorimeters may be used. The heat of combustion is a measure of the energy available from a fuel. A knowledge of this value is essential when considering the thermal efficiency of equipment for producing either power or heat.

  13. A revised 5 minute gravimetric geoid and associated errors for the North Atlantic calibration area

    NASA Technical Reports Server (NTRS)

    Mader, G. L.

    1979-01-01

    A revised 5 minute gravimetric geoid and its errors were computed for the North Atlantic calibration area using GEM-8 potential coefficients and the latest gravity data available from the Defense Mapping Agency. This effort was prompted by a number of inconsistencies and small errors found in previous calculations of this geoid. The computational method and constants used are given in detail to serve as a reference for future work.

  14. A detailed gravimetric geoid from North America to Eurasia

    NASA Technical Reports Server (NTRS)

    Vincent, S. F.; Strange, W. E.; Marsh, J. G.

    1972-01-01

    A detailed gravimetric geoid of the United States, North Atlantic, and Eurasia, which was computed from a combination of satellite derived and surface gravity data, is presented. The precision of this detailed geoid is + or - 2 to + or - 3 m in the continents but may be in the range of 5 to 7 m in those areas where data is sparse. Comparisons of the detailed gravimetric geoid with results of Rapp, Fischer, and Rice for the United States, Bomford in Europe, and Heiskanen and Fischer in India are presented. Comparisons are also presented with geoid heights from satellite solutions for geocentric station coordinates in North America, the Caribbean, and Europe.

  15. Method for reducing the sulfur content of a sulfur-containing hydrocarbon stream

    DOEpatents

    Mahajan, Devinder

    2004-12-28

    The sulfur content of a liquid hydrocarbon stream is reduced under mild conditions by contracting a sulfur-containing liquid hydrocarbon stream with transition metal particles containing the transition metal in a zero oxidation state under conditions sufficient to provide a hydrocarbon product having a reduced sulfur content and metal sulfide particles. The transition metal particles can be produced in situ by adding a transition metal precursor, e.g., a transition metal carbonyl compound, to the sulfur-containing liquid feed stream and sonicating the feed steam/transition metal precursor combination under conditions sufficient to produce the transition metal particles.

  16. Method for converting hydrocarbon fuel into hydrogen gas and carbon dioxide

    DOEpatents

    Clawson, Lawrence G.; Mitchell, William L.; Bentley, Jeffrey M.; Thijssen, Johannes H. J.

    2000-01-01

    A method for converting hydrocarbon fuel into hydrogen gas and carbon dioxide within a reformer 10 is disclosed. According to the method, a stream including an oxygen-containing gas is directed adjacent to a first vessel 18 and the oxygen-containing gas is heated. A stream including unburned fuel is introduced into the oxygen-containing gas stream to form a mixture including oxygen-containing gas and fuel. The mixture of oxygen-containing gas and unburned fuel is directed tangentially into a partial oxidation reaction zone 24 within the first vessel 18. The mixture of oxygen-containing gas and fuel is further directed through the partial oxidation reaction zone 24 to produce a heated reformate stream including hydrogen gas and carbon monoxide. Steam may also be mixed with the oxygen-containing gas and fuel, and the reformate stream from the partial oxidation reaction zone 24 directed into a steam reforming zone 26. High- and low-temperature shift reaction zones 64,76 may be employed for further fuel processing.

  17. A comprehensive two-dimensional gas chromatography method for analyzing extractable petroleum hydrocarbons in water and soil.

    PubMed

    Seeley, Stacy K; Bandurski, Steven V; Brown, Robert G; McCurry, James D; Seeley, John V

    2007-01-01

    A flow-switching two-dimensional gas chromatography (GCxGC) apparatus has been constructed that can operate at temperatures as high as 340 degrees C. This system is employed to analyze complex hydrocarbon mixtures such as diesel fuel, gas-oil, motor oil, and petroleum contaminated environmental samples. The GCxGC system generates two-dimensional chromatograms with minimal overlap between the aliphatic and aromatic regions This allows these compound classes to be independently quantitated without prior fractionation. The GCxGC system is used to analyze extracts of spiked water samples, wastewater, and soil. The accuracy of the method is compared to that of the Massachusetts Extractable Petroleum Hydrocarbons (MA EPH) method. The GCxGC system generates a quantitative accuracy similar to the MA EPH method for the analysis of spiked water samples. The GCxGC method and the MA EPH method generate comparable levels of total hydrocarbons when wastewater is analyzed, but the GCxGC method detects a significantly higher aromatic content and lower aliphatic content. Both the GCxGC method and MA EPH method measure comparable levels of aromatics in the soil samples. PMID:18078573

  18. 40 CFR 1065.290 - PM gravimetric balance.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 34 2013-07-01 2013-07-01 false PM gravimetric balance. 1065.290 Section 1065.290 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR POLLUTION CONTROLS ENGINE-TESTING PROCEDURES Measurement Instruments Pm Measurements § 1065.290 PM...

  19. 40 CFR 1065.290 - PM gravimetric balance.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 32 2010-07-01 2010-07-01 false PM gravimetric balance. 1065.290 Section 1065.290 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR POLLUTION CONTROLS ENGINE-TESTING PROCEDURES Measurement Instruments Pm Measurements § 1065.290 PM...

  20. 40 CFR 1065.290 - PM gravimetric balance.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 33 2011-07-01 2011-07-01 false PM gravimetric balance. 1065.290 Section 1065.290 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR POLLUTION CONTROLS ENGINE-TESTING PROCEDURES Measurement Instruments Pm Measurements § 1065.290 PM...

  1. 40 CFR 1065.290 - PM gravimetric balance.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 33 2014-07-01 2014-07-01 false PM gravimetric balance. 1065.290 Section 1065.290 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR POLLUTION CONTROLS ENGINE-TESTING PROCEDURES Measurement Instruments Pm Measurements § 1065.290 PM...

  2. 40 CFR 1065.290 - PM gravimetric balance.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 34 2012-07-01 2012-07-01 false PM gravimetric balance. 1065.290 Section 1065.290 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR POLLUTION CONTROLS ENGINE-TESTING PROCEDURES Measurement Instruments Pm Measurements § 1065.290 PM...

  3. Determination of Phosphates by the Gravimetric Quimociac Technique

    ERIC Educational Resources Information Center

    Shaver, Lee Alan

    2008-01-01

    The determination of phosphates by the classic quimociac gravimetric technique was used successfully as a laboratory experiment in our undergraduate analytical chemistry course. Phosphate-containing compounds are dissolved in acid and converted to soluble orthophosphate ion (PO[subscript 4][superscript 3-]). The soluble phosphate is easily…

  4. Decomposition of Copper (II) Sulfate Pentahydrate: A Sequential Gravimetric Analysis.

    ERIC Educational Resources Information Center

    Harris, Arlo D.; Kalbus, Lee H.

    1979-01-01

    Describes an improved experiment of the thermal dehydration of copper (II) sulfate pentahydrate. The improvements described here are control of the temperature environment and a quantitative study of the decomposition reaction to a thermally stable oxide. Data will suffice to show sequential gravimetric analysis. (Author/SA)

  5. Evaluation of gravimetric techniques to estimate the microvascular filtration coefficient.

    PubMed

    Dongaonkar, R M; Laine, G A; Stewart, R H; Quick, C M

    2011-06-01

    Microvascular permeability to water is characterized by the microvascular filtration coefficient (K(f)). Conventional gravimetric techniques to estimate K(f) rely on data obtained from either transient or steady-state increases in organ weight in response to increases in microvascular pressure. Both techniques result in considerably different estimates and neither account for interstitial fluid storage and lymphatic return. We therefore developed a theoretical framework to evaluate K(f) estimation techniques by 1) comparing conventional techniques to a novel technique that includes effects of interstitial fluid storage and lymphatic return, 2) evaluating the ability of conventional techniques to reproduce K(f) from simulated gravimetric data generated by a realistic interstitial fluid balance model, 3) analyzing new data collected from rat intestine, and 4) analyzing previously reported data. These approaches revealed that the steady-state gravimetric technique yields estimates that are not directly related to K(f) and are in some cases directly proportional to interstitial compliance. However, the transient gravimetric technique yields accurate estimates in some organs, because the typical experimental duration minimizes the effects of interstitial fluid storage and lymphatic return. Furthermore, our analytical framework reveals that the supposed requirement of tying off all draining lymphatic vessels for the transient technique is unnecessary. Finally, our numerical simulations indicate that our comprehensive technique accurately reproduces the value of K(f) in all organs, is not confounded by interstitial storage and lymphatic return, and provides corroboration of the estimate from the transient technique.

  6. Evaluation of gravimetric techniques to estimate the microvascular filtration coefficient.

    PubMed

    Dongaonkar, R M; Laine, G A; Stewart, R H; Quick, C M

    2011-06-01

    Microvascular permeability to water is characterized by the microvascular filtration coefficient (K(f)). Conventional gravimetric techniques to estimate K(f) rely on data obtained from either transient or steady-state increases in organ weight in response to increases in microvascular pressure. Both techniques result in considerably different estimates and neither account for interstitial fluid storage and lymphatic return. We therefore developed a theoretical framework to evaluate K(f) estimation techniques by 1) comparing conventional techniques to a novel technique that includes effects of interstitial fluid storage and lymphatic return, 2) evaluating the ability of conventional techniques to reproduce K(f) from simulated gravimetric data generated by a realistic interstitial fluid balance model, 3) analyzing new data collected from rat intestine, and 4) analyzing previously reported data. These approaches revealed that the steady-state gravimetric technique yields estimates that are not directly related to K(f) and are in some cases directly proportional to interstitial compliance. However, the transient gravimetric technique yields accurate estimates in some organs, because the typical experimental duration minimizes the effects of interstitial fluid storage and lymphatic return. Furthermore, our analytical framework reveals that the supposed requirement of tying off all draining lymphatic vessels for the transient technique is unnecessary. Finally, our numerical simulations indicate that our comprehensive technique accurately reproduces the value of K(f) in all organs, is not confounded by interstitial storage and lymphatic return, and provides corroboration of the estimate from the transient technique. PMID:21346245

  7. Method And Apparatus For Converting Hydrocarbon Fuel Into Hydrogen Gas And Carbon Dioxide

    DOEpatents

    Clawson, Lawrence G.; Mitchell, William L.; Bentley, Jeffrey M.; Thijssen, Johannes H. J.

    2000-09-26

    A method is disclosed for synthesizing hydrogen gas from hydrocarbon fuel. A first mixture of steam and a first fuel is directed into a first tube 208 to subject the first mixture to a first steam reforming reaction in the presence of a first catalyst 214. A stream of oxygen-containing gas is pre-heated by transferring heat energy from product gases. A second mixture of the pre-heated oxygen-containing gas and a second fuel is directed into a second tube 218 disposed about the first tube 208 to subject the second mixture to a partial oxidation reaction and to provide heat energy for transfer to the first tube 208. A first reaction reformate from the first tube 208 and a second reaction reformate from the second tube 218 are directed into a third tube 224 disposed about the second tube 218 to subject the first and second reaction reformates to a second steam reforming reaction, wherein heat energy is transferred to the third tube 224 from the second tube 218.

  8. Method and apparatus for converting hydrocarbon fuel into hydrogen gas and carbon dioxide

    DOEpatents

    Clawson, Lawrence G.; Mitchell, William L.; Bentley, Jeffrey M.; Thijssen, Johannes H.J.

    2000-01-01

    An apparatus and a method are disclosed for converting hydrocarbon fuel or an alcohol into hydrogen gas and carbon dioxide. The apparatus includes a first vessel having a partial oxidation reaction zone and a separate steam reforming reaction zone that is distinct from the partial oxidation reaction zone. The first vessel has a first vessel inlet at the partial oxidation reaction zone and a first vessel outlet at the steam reforming zone. The reformer also includes a helical tube extending about the first vessel. The helical tube has a first end connected to an oxygen-containing source and a second end connected to the first vessel at the partial oxidation reaction zone. Oxygen gas from an oxygen-containing source can be directed through the helical tube to the first vessel. A second vessel having a second vessel inlet and second vessel outlet is annularly disposed about the first vessel. The helical tube is disposed between the first vessel and the second vessel and gases from the first vessel can be directed through second vessel.

  9. Detection of polycyclic aromatic hydrocarbons (PAHs) in raw menhaden fish oil using fluorescence spectroscopy: Method development.

    PubMed

    Pena, Edwin A; Ridley, Lauren M; Murphy, Wyatt R; Sowa, John R; Bentivegna, Carolyn S

    2015-09-01

    Raw menhaden fish oil was developed for biomonitoring polycyclic aromatic hydrocarbons (PAHs) using fluorescence spectroscopy. Menhaden (Genus Brevoortia) were collected in 2010 and/or 2011 from Delaware Bay, New Jersey, USA; James River, Virginia, USA; Vermillion Bay, Louisiana, USA (VBLA); and Barataria Bay, Louisiana, USA (BBLA). Barataria Bay, Louisiana received heavy oiling from the Deepwater Horizon oil spill. Method development included determining optimal wavelengths for PAH detection, fish oil matrix interferences, and influence of solvent concentration on extraction. Results showed that some fish oils contained high molecular weight PAH-like compounds in addition to other fluorescent compounds such as albumin and vitamin A and vitamin E. None of these naturally occurring compounds interfered with detection of high molecular weight PAHs. However, data suggested that the lipid component of fish oil was altering fluorescence spectra by supporting the formation of PAH excimers. For example, the most intense excitation wavelength for hydroxypyrene shifted from Ex285/Em430 to Ex340/Em430. Comparison of Deepwater Horizon crude oil and fish oil spectra indicated that some fish oils contained crude oil-like PAHs. Using wavelengths of Ex360/Em430, fish oil concentrations were calculated as 3.92 μg/g, 0.61 μg/g, and 0.14 μg/g for a Delaware Bay sample, BBLA 2011, and VBLA 2011, respectively. Overall, these results supported using menhaden fish oil to track PAH exposures spatially and temporally.

  10. Potential of preliminary test methods to predict biodegradation performance of petroleum hydrocarbons in soil.

    PubMed

    Aichberger, H; Hasinger, Marion; Braun, Rudolf; Loibner, Andreas P

    2005-03-01

    Preliminary tests at different scales such as degradation experiments (laboratory) in shaking flasks, soil columns and lysimeters as well as in situ respiration tests (field) were performed with soil from two hydrocarbon contaminated sites. Tests have been evaluated in terms of their potential to provide information on feasibility, degradation rates and residual concentration of bioremediation in the vadose zone. Sample size, costs and duration increased with experimental scale in the order shaking flasks - soil columns - lysimeter - in situ respiration tests, only time demand of respiration tests was relatively low. First-order rate constants observed in degradation experiments exhibited significant differences between both, different experimental sizes and different soils. Rates were in line with type and history of contamination at the sites, but somewhat overestimated field rates particularly in small scale experiments. All laboratory experiments allowed an estimation of residual concentrations after remediation. In situ respiration tests were found to be an appropriate pre-testing and monitoring tool for bioventing although residual concentrations cannot be predicted from in situ respiration tests. Moreover, this method does not account for potential limitations that might hamper biodegradation in the longer term but only reflects the actual degradation potential when the test is performed.

  11. Application of various methods for removal of polycyclic aromatic hydrocarbons from synthetic solid matrices.

    PubMed

    Karaca, Gizem; Tasdemir, Yücel

    2014-08-01

    In the present study, removal of polycyclic aromatic hydrocarbons (PAHs) from synthetic solid matrices with various methods was investigated. PAH removal experiments were conducted in a specifically designed UV apparatus for this study. Polyurethane foams (PUF) cartridges were used to remove PAHs from the incoming air and to capture PAHs from the evaporated gases. Sodium sulphate (Na2SO4) was used as a synthetic solid matrices. The effects of temperature, UV radiation, titanium dioxide (TiO2) and diethylamine (DEA) dose on the PAH removal were determined. TiO2and DEA were added to the Na2SO4 sample at the rate of 5% and 20% of dry weight of samples. PAHs' removal from the Na2SO4 enhanced with increasing temperature. Sigma12 PAH content in the Na2SO4 reduced up to 95% during UV light application. Moreover, the Sigma12 PAH removal ratio was calculated as 95% with using 5% of TiO2, and increasing of TiO2 dose negatively affected PAH removal. PAH concentration in the samples decreased by 93% and 99% with addition of 5% and 20% DEA, respectively. Especially, 3- and 4-ring PAH compounds evaporated during the PAH removal applications. As expected, evaporation mechanism became more effective at high temperature for light PAH compounds. It was concluded that PAHs can successfully be removed from synthetic solid matrices such as Na2 SO4 with the applications of UV light and UV-photocatalysts.

  12. Detection of polycyclic aromatic hydrocarbons (PAHs) in raw menhaden fish oil using fluorescence spectroscopy: Method development.

    PubMed

    Pena, Edwin A; Ridley, Lauren M; Murphy, Wyatt R; Sowa, John R; Bentivegna, Carolyn S

    2015-09-01

    Raw menhaden fish oil was developed for biomonitoring polycyclic aromatic hydrocarbons (PAHs) using fluorescence spectroscopy. Menhaden (Genus Brevoortia) were collected in 2010 and/or 2011 from Delaware Bay, New Jersey, USA; James River, Virginia, USA; Vermillion Bay, Louisiana, USA (VBLA); and Barataria Bay, Louisiana, USA (BBLA). Barataria Bay, Louisiana received heavy oiling from the Deepwater Horizon oil spill. Method development included determining optimal wavelengths for PAH detection, fish oil matrix interferences, and influence of solvent concentration on extraction. Results showed that some fish oils contained high molecular weight PAH-like compounds in addition to other fluorescent compounds such as albumin and vitamin A and vitamin E. None of these naturally occurring compounds interfered with detection of high molecular weight PAHs. However, data suggested that the lipid component of fish oil was altering fluorescence spectra by supporting the formation of PAH excimers. For example, the most intense excitation wavelength for hydroxypyrene shifted from Ex285/Em430 to Ex340/Em430. Comparison of Deepwater Horizon crude oil and fish oil spectra indicated that some fish oils contained crude oil-like PAHs. Using wavelengths of Ex360/Em430, fish oil concentrations were calculated as 3.92 μg/g, 0.61 μg/g, and 0.14 μg/g for a Delaware Bay sample, BBLA 2011, and VBLA 2011, respectively. Overall, these results supported using menhaden fish oil to track PAH exposures spatially and temporally. PMID:25867932

  13. Effect of seeds on bile-enzymatic-gravimetric analysis of total dietary fiber.

    PubMed

    Cranker, K J; Phillips, K M; Gonzales, M C; Stewart, K K

    1997-01-01

    Dietary fiber sometimes is defined chemically as nonstarch polysaccharides plus lignin or as other specific chemical entities. Analysis of dietary fiber according to a chemical definition typically involves gas chromatography, which allows separation and quantitation of chemical constituents that are added to arrive at a dietary fiber value. Other definitions of fiber are broader, defining it to be whatever is not digested in the alimentary tract. Analytically, this definition translates into the gravimetric sum of the material remaining after a series of enzymatic and chemical treatments that simulate in vivo digestion. Various methods reflect the gravimetric definition, which might include as dietary fiber some protein, resistant starch, and even lipids that are not digested by particular assay conditions. We used a recently proposed bile-enzymatic-gravimetric assay for total dietary fiber on commonly consumed seeds (hulled and unhulled sesame, caraway, and poppy) and visually found these seeds to be undigested. We then determined the impact of the undigested seeds on measured dietary fiber content by spiking homogenized daily menus with 5% by weight of these seeds and calculating recoveries with 2 assumptions: seeds are 100% fiber because they are not digested, and the fiber content of seeds is as determined by assay. Calculated recoveries were very different depending on which assumption was made (71-90% or 99-109%, respectively), and the difference was closely related to the seed's protein content.

  14. Resonant efficiency improvement design of piezoelectric biosensor for bacteria gravimetric sensing.

    PubMed

    Tsai, Jang-Zern; Chen, Ching-Jung; Shie, Dung-Ting; Liu, Jen-Tsai

    2014-01-01

    The piezoelectric biosensor have been widely used in ultra-small mass detection of biomolecular, based on PZT piezoelectric material can create a variety of compositions geometrically; it could widely develop a high-frequency resonator and measure the change of the slightest mass while improve the limited detection simultaneously. Therefore, the piezoelectric biosensor of this study was fabricated by a spin-coating method and backside etching process for improving the characteristic of piezoelectric biosensor. The result exhibited that the 250 μm × 250 μm working size has the most favorable piezoelectric characteristic. The tunability was approximately 38.56 % and it showed that reducing the substrate thickness could obtain a clear resonance signal in a range of 60 to 380 MHz. In theory calculated for gravimetric sensing, it could achieve 0.1 ng sensing sensitivity. In gravimetric sensing, the sensing range was between 50,000~100,000 CFU/ml. Sensing range was lower in clinical urinary tract infection (100,000 CFU/ml), thus demonstrating its usefulness for preventive medicine. It can understand the piezoelectric sensor of this study has potential application in the future for biomedical gravimetric sensing.

  15. A New, Rapid, Precise and Sensitive Method for Chlorine Stable Isotope Analysis of Chlorinated Aliphatic Hydrocarbons

    NASA Astrophysics Data System (ADS)

    van Acker, M. R.; Shahar, A.; Young, E. D.; Coleman, M. L.

    2005-12-01

    Chlorinated aliphatic hydrocarbons (CAH) are recognized common groundwater contaminants. Because of their physico-chemical properties, their lifespan in groundwater is in the order of decades (Pankow and Cherry, 1996). Stable isotopes can play a role in determining the rate and extent of CAH attenuation (Slater, 2003). The use of chlorine has been hampered by the current time consuming and insensitive analytical methods. We present a new analytical procedure to measure chlorine stable isotope values using a gas chromatograph coupled to a multi-collector inductively coupled mass spectrometer (GC-MC-ICP-MS). The GC has a Porapack Q packed column. The carrier gas was helium and the temperature was constant at 160°C. The GC was coupled to the MC-ICP-MS by heated stainless steel tubing. Our high resolution spectra showed that 37Cl is free of its main interference 36Ar-H over a range of 0.004 amu. Two pure CAH, trichloroethene (TCE) and tetrachloroethene (PCE), were used for zero enrichment (sample relative to itself) and standard-sample difference measurements. Integrations and background corrections of transient signals were performed using Microsoft Excel after import of the raw data from the MC-ICPMS acquisition software. Zero enrichment tests with TCE and PCE yielded δ37Cl of -0.04±0.16‰ and -0.03±0.17‰, respectively, results for sample injections of 0.12 to 0.02 microliters. Accuracy was tested by injecting 0.24 microliters of a 50/50 mixture of TCE and PCE of known isotopic compositions as the difference between the two solvents was of paramount interest. The δ37Cl(TCE) value of PCE was -1.99±0.16‰. A highly satisfactory comparison with the conventional method is shown by published values for TCE and PCE, -2.04±0.12‰ and -0.30±0.14‰, respectively (Jendrzejewski et al., 2001), giving a δ37Cl(TCE) value for PCE of -2.34±0.18‰. These tests of the GC-MC-ICP-MS method showed that we can obtain reproducible and accurate Cl isotope values using an

  16. A Simple Method for Estimation of Dielectric Constants and Polarizabilities of Nonpolar and Slightly Polar Hydrocarbons

    NASA Astrophysics Data System (ADS)

    Panuganti, Sai R.; Wang, Fei; Chapman, Walter G.; Vargas, Francisco M.

    2016-07-01

    Many of the liquids that are used as electrical insulators are nonpolar or slightly polar petroleum-derived hydrocarbons, such as the ones used for cable and/or transformer oils. In this work, semi-empirical expressions with no adjustable parameters for the dielectric constant and the polarizability of nonpolar and slightly polar hydrocarbons and their mixtures are proposed and validated. The expressions that were derived using the Vargas-Chapman One-Third rule require the mass density and the molecular weight of the substance of interest. The equations were successfully tested for various hydrocarbons and polymers with dipole moments <0.23 and densities from 500 to 1200 kg\\cdot hbox {m}^{-3}. The predictions are in good agreement with the experimental data in a wide range of temperatures and pressures. The proposed expressions eliminate the need of extensive experimental data and require less input parameters compared to existing correlations.

  17. Sampling and analytical method development and hand wipe measurements of dermal exposures to polycyclic aromatic hydrocarbons.

    PubMed

    Boeniger, Mark; Neumeister, Charles; Booth-Jones, Angela

    2008-07-01

    This article describes the laboratory assessment of a hand and surface wipe sampling method for polycyclic aromatic hydrocarbons (PAHs). The analytical method employed extraction of the wipe samples into dimethyl sulfoxide (DMSO) and high-performance liquid chromatography (HPLC) flourometric detection of pyrene, a predominant PAH in used gasoline engine oils (UGEO). Recovery of pyrene was evaluated for two different sampling media by first contaminating the hands of a small number of volunteers with UGEO, followed by applying a small amount of corn oil to the palms, and by wiping the skin with a Whatman cellulostic filter paper or a polyester fabric wipe (i.e., Alpha wipes). In summary, using either Whatman or Alpha wipes, the mean recovery of pyrene from the UGEO that was applied to the hands and contained within three consecutive wipes was 69% and 54%, respectively. However, the relative recovery of the first to second wipe was on average 47% and 75% for the two media, respectively. These results indicate that the Alpha wipes were more efficient at recovering pyrene in the first wipe but less efficient overall when all three consecutive samples were included. Even though this sampling was performed in a controlled laboratory environment, the minimum and maximum amount of pyrene recovered in the individual composite samples using either method spanned a range of twofold. Overall, intra-and interpersonal variability, as measured by coefficient of variation, were 22% and 19%, respectively, and were not statistically different by type of media used. This method was used in a pilot field survey to sample the hands of 18 automotive repair technicians and 18 office workers. Detectable amounts of pyrene (>0.2 microg/sample) were found on the hands of 61% and 0% of these two groups, respectively, with the highest measured quantity equal to 1.06 microg. Samples from the upper surfaces of automobile motors were generally low to nondetectable (<0.027 microg/sample), while

  18. Apparatus and method for simultaneous recovery of hydrogen from water and from hydrocarbons

    DOEpatents

    Willms, R. Scott; Birdsell, Stephen A.

    2000-01-01

    Apparatus and method for simultaneous recovery of hydrogen from water and from hydrocarbon feed material. The feed material is caused to flow over a heated catalyst which fosters the water-gas shift reaction (H.sub.2 O+COH.sub.2 +CO.sub.2) and the methane steam reforming reaction (CH.sub.4 +H.sub.2 O3 H.sub.2 +CO). Both of these reactions proceed only to partial completion. However, by use of a Pd/Ag membrane which is exclusively permeable to hydrogen isotopes in the vicinity of the above reactions and by maintaining a vacuum on the permeate side of the membrane, product hydrogen isotopes are removed and the reactions are caused to proceed further toward completion. A two-stage palladium membrane reactor was tested with a feed composition of 28% CQ.sub.4, 35% Q.sub.2 O (where Q=H, D, or T), and 31% Ar in 31 hours of continuous operation during which 4.5 g of tritium were processed. Decontamination factors were found to increase with decreasing inlet rate. The first stage was observed to have a decontamination factor of approximately 200, while the second stage had a decontamination factor of 2.9.times.10.sup.6. The overall decontamination factor was 5.8.times.10.sup.8. When a Pt/.alpha.-Al.sub.2 O.sub.3 catalyst is employed, decoking could be performed without catalyst degradation. However, by adjusting the carbon to oxygen ratio of the feed material with the addition of oxygen, coking could be altogether avoided.

  19. Characterization of the relationship between microbial degradation processes at a hydrocarbon contaminated site using isotopic methods.

    PubMed

    Feisthauer, Stefan; Seidel, Martin; Bombach, Petra; Traube, Sebastian; Knöller, Kay; Wange, Martin; Fachmann, Stefan; Richnow, Hans H

    2012-05-15

    Decisions to employ monitored natural attenuation (MNA) as a remediation strategy at contaminated field sites require a comprehensive characterization of the site-specific biodegradation processes. In the present study, compound-specific carbon and hydrogen isotope analysis (CSIA) was used to investigate intrinsic biodegradation of benzene and ethylbenzene in an aquifer with high levels of aromatic and aliphatic hydrocarbon contamination. Hydrochemical data and isotope fractionation analysis of sulfate and methane was used complementarily to elucidate microbial degradation processes over the course of a three year period, consisting of six sampling campaigns, in the industrial area of Weißandt-Gölzau (Saxony-Anhalt, Germany). Enrichment of (13)C and (2)H isotopes in the residual benzene and ethylbenzene pool downgradient from the pollution sources provided evidence of biodegradation of BTEX compounds at this site, targeting both compounds as the key contaminants of concern. The enrichment of heavy sulfur isotopes accompanied by decreasing sulfate concentrations and the accumulation of isotopically light methane suggested that sulfate-reducing and methanogenic processes are the major contributors to overall biodegradation in this aquifer. Along the contaminant plume, the oxidation of methane with δ(13)C(CH4) values of up to +17.5‰ was detected. This demonstrates that methane formed in the contaminant source can be transported along groundwater flow paths and be oxidized in areas with higher redox potentials, thereby competing directly with the pollutants for electron acceptors. Hydrochemical and isotope data was summarized in a conceptual model to assess whether MNA can be used as viable remediation strategy in Weißandt-Gölzau. The presented results demonstrate the benefits of combining different isotopic methods and hydrochemical approaches to evaluate the fate of organic pollutants in contaminated aquifers.

  20. Use of thermal desorption/gas chromatography as a performance-based screening method for petroleum hydrocarbons

    SciTech Connect

    Slavin, P.J. |; Crandall, K.; Dawson, L.; Kottenstette, R.; Wade, M. |

    1996-08-01

    Thermal desorption/gas chromatography (TD/GC) was used to screen soil samples on site for total petroleum hydrocarbon (TPH) content during a RCRA Facility Investigation (RFI). It proved to be a rapid, cost- effective tool for detecting non-aromatic mineral oil in soil. The on- site TD/GC results correlated well with those generated at an off- site laboratory for samples analyzed in accordance with EPA Method 418.1.

  1. A detailed gravimetric geoid of North America, Eurasia, and Australia

    NASA Technical Reports Server (NTRS)

    Vincent, S.; Strange, W. E.

    1972-01-01

    A detailed gravimetric geoid of North America, the North Atlantic, Eurasia, and Australia computed from a combination of satellite-derived and surface 1 x 1 gravity data, is presented. Using a consistent set of parameters, this geoid is referenced to an absolute datum. The precision of this detailed geoid is + or - 2 meters in the continents but may be in the range of 5 to 7 meters in those areas where data was sparse. Comparisons of the detailed gravimetric geoid with results of Rice for the United States, Bomford and Fischer in Eurasia, and Mather in Australia are presented. Comparisons are also presented with geoid heights from satellite solutions for geocentric station coordinates in North America, the Caribbean, Europe, and Australia.

  2. Correction factors for gravimetric measurement of peritumoural oedema in man.

    PubMed

    Bell, B A; Smith, M A; Tocher, J L; Miller, J D

    1987-01-01

    The water content of samples of normal and oedematous brain in lobectomy specimens from 16 patients with cerebral tumours has been measured by gravimetry and by wet and dry weighing. Uncorrected gravimetry underestimated the water content of oedematous peritumoural cortex by a mean of 1.17%, and of oedematous peritumoural white matter by a mean of 2.52%. Gravimetric correction equations calculated theoretically and from an animal model of serum infusion white matter oedema overestimate peritumoural white matter oedema in man, and empirical gravimetric error correction factors for oedematous peritumoural human white matter and cortex have therefore been derived. These enable gravimetry to be used to accurately determine peritumoural oedema in man. PMID:3268140

  3. Correction factors for gravimetric measurement of peritumoural oedema in man.

    PubMed

    Bell, B A; Smith, M A; Tocher, J L; Miller, J D

    1987-01-01

    The water content of samples of normal and oedematous brain in lobectomy specimens from 16 patients with cerebral tumours has been measured by gravimetry and by wet and dry weighing. Uncorrected gravimetry underestimated the water content of oedematous peritumoural cortex by a mean of 1.17%, and of oedematous peritumoural white matter by a mean of 2.52%. Gravimetric correction equations calculated theoretically and from an animal model of serum infusion white matter oedema overestimate peritumoural white matter oedema in man, and empirical gravimetric error correction factors for oedematous peritumoural human white matter and cortex have therefore been derived. These enable gravimetry to be used to accurately determine peritumoural oedema in man.

  4. Discriminating DNA mismatches by electrochemical and gravimetric techniques.

    PubMed

    Mazouz, Zouhour; Fourati, Najla; Zerrouki, Chouki; Ommezine, Asma; Rebhi, Lamia; Yaakoubi, Nourdin; Kalfat, Rafik; Othmane, Ali

    2013-10-15

    A silicon nitride functionalized electrode and a 104 MHz lithium tantalate (LiTaO₃) surface acoustic wave (SAW) sensor have been used to investigate target-probe recognition processes. Electrochemical and gravimetric measurements have been considered to monitor hybridization of single base mismatch (SBM) in synthetic oligonucleotides and single-nucleotide polymorphisms ApoE in real clinical genotypes. Obvious discrimination of SBM in nucleotides has been shown by both gravimetric and electrochemical techniques, without labeling nor amplification. Investigations on mismatches nature and position have also been considered. For guanine-adenine (GA), guanine-thymine (GT) and guanine-guanine (GG) mismatches, the sensors responses present a dependence upon positions. Considering the capacitance variations and hybridization rates, results showed that gravimetric transduction is more sensitive than electrochemical one. Moreover, the highest value of GT hybridization rate (in the middle position) was found in accordance with the nearest-neighbor model, where the considered configuration appears as the most thermodynamically stable. For the real samples, where the electrochemical transduction, by combining capacitance and flat-band potential measurements, were found more sensitive, the results show that the realized sensor permits an unambiguous discrimination of recognition between fully complementary, non-complementary and single base mismatched targets, and even between the combination of differently matched strands.

  5. MODELS AND METHODS FOR PETROLEUM HYDROCARBON RISK ASSESSMENT: ONSITE, LUSTRISK, AND HSSM

    EPA Science Inventory

    U.S. EPA has developed three tiers of models for analysis of fuel releases from underground storage tank (UST) systems: 1) OnSite; 2) LUSTRisk, and 3) the Hydrocarbon Spill Screening Model (HSSM). The tiered approach to modeling allows users to select a model based upon the amoun...

  6. Subtask 1.20 - Development of Methods to Determine the Environmental Availability of PAHs, PCBs, and Petroleum Hydrocarbons

    SciTech Connect

    Steven Hawthorne

    2007-06-30

    Three methods to determine the bioavailability of polycyclic aromatic hydrocarbons were modified and developed for application to polychlorinated biphenyls (PCBs). Water/XAD desorption and selective supercritical fluid extraction methods were developed to determine the rapidly-released fraction of PCBs from contaminated soils and sediments. A method to determine PCBs in sediment pore water based on solid-phase microextraction was also developed that is capable of determining low pg/mL concentrations with water samples as small as 1.5 mL.

  7. Apparatus and methods for direct conversion of gaseous hydrocarbons to liquids

    DOEpatents

    Kong, Peter C.; Lessing, Paul A.

    2006-04-25

    A chemical reactor for direct conversion of hydrocarbons includes a dielectric barrier discharge plasma cell and a solid oxide electrochemical cell in fluid communication therewith. The discharge plasma cell comprises a pair of electrodes separated by a dielectric material and passageway therebetween. The electrochemical cell comprises a mixed-conducting solid oxide electrolyte membrane tube positioned between a porous cathode and a porous anode, and a gas inlet tube for feeding oxygen containing gas to the porous cathode. An inlet is provided for feeding hydrocarbons to the passageway of the discharge plasma cell, and an outlet is provided for discharging reaction products from the reactor. A packed bed catalyst may optionally be used in the reactor to increase efficiency of conversion. The reactor can be modified to allow use of a light source for directing ultraviolet light into the discharge plasma cell and the electrochemical cell.

  8. A method for measuring electrokinetic coefficients of porous media and its potential application in hydrocarbon exploration

    NASA Astrophysics Data System (ADS)

    Jiang, Y. G.; Shan, F. K.; Jin, H. M.; Zhou, L. W.; Sheng, Ping

    We have designed and constructed a compact cell to measure the electrokinetic coefficients in the frequency range of interest to hydrocarbon exploration, 20 to 100 Hz. Experimental results are presented on the frequency dependence of the electrokinetic coefficients, and dynamic permeability of a porous rock saturated with either 0.1 mole brine or transformer oil. In particular, the brine-saturated electro-osmosis coefficient is found to be two orders of magnitude larger than that saturated with transformer oil; whereas for the streaming potential the ratio of the two cases is in the reverse. These results, when combined with viscosity and electrical conductivity values, lead consistently to the fact that the electrokinetic Onsager coefficient of brine-saturated samples is three orders of magnitude larger than that of oil-saturated samples. This difference provides a strong motivation to further explore the potential application of electrokinetic Onsager coefficient as a hydrocarbon indicator.

  9. Method for forming a potential hydrocarbon sensor with low sensitivity to methane and CO

    DOEpatents

    Mukundan, Rangachary; Brosha, Eric L.; Garzon, Fernando

    2003-12-02

    A hydrocarbon sensor is formed with an electrolyte body having a first electrolyte surface with a reference electrode depending therefrom and a metal oxide electrode body contained within the electrolyte body and having a first electrode surface coplanar with the first electrolyte surface. The sensor was formed by forming a sintered metal-oxide electrode body and placing the metal-oxide electrode body within an electrolyte powder. The electrolyte powder with the metal-oxide electrode body was pressed to form a pressed electrolyte body containing the metal-oxide electrode body. The electrolyte was removed from an electrolyte surface above the metal-oxide electrode body to expose a metal-oxide electrode surface that is coplanar with the electrolyte surface. The electrolyte body and the metal-oxide electrode body were then sintered to form the hydrocarbon sensor.

  10. Novel Approach for Evaluating Secondary Organic Aerosol from Aromatic Hydrocarbons: Unified Method for Predicting Aerosol Composition and Formation.

    PubMed

    Li, Lijie; Tang, Ping; Nakao, Shunsuke; Kacarab, Mary; Cocker, David R

    2016-06-21

    Innovative secondary organic aerosol (SOA) composition analysis methods normalizing aerosol yield and chemical composition on an aromatic ring basis are developed and utilized to explore aerosol formation from oxidation of aromatic hydrocarbons. SOA yield and chemical composition are revisited using 15 years of University of California, Riverside/CE-CERT environmental chamber data on 17 aromatic hydrocarbons with HC:NO ranging from 11.1 to 171 ppbC:ppb. SOA yield is redefined in this work by normalizing the molecular weight of all aromatic precursors to the molecular weight of the aromatic ring [Formula: see text], where i is the aromatic hydrocarbon precursor. The yield normalization process demonstrates that the amount of aromatic rings present is a more significant driver of aerosol formation than the vapor pressure of the precursor aromatic. Yield normalization also provided a basis to evaluate isomer impacts on SOA formation. Further, SOA elemental composition is explored relative to the aromatic ring rather than on a classical mole basis. Generally, four oxygens per aromatic ring are observed in SOA, regardless of the alkyl substitutes attached to the ring. Besides the observed SOA oxygen to ring ratio (O/R ∼ 4), a hydrogen to ring ratio (H/R) of 6 + 2n is observed, where n is the number of nonaromatic carbons. Normalization of yield and composition to the aromatic ring clearly demonstrates the greater significance of aromatic ring carbons compared with alkyl carbon substituents in determining SOA formation and composition. PMID:27177154

  11. Method of Generating Hydrocarbon Reagents from Diesel, Natural Gas and Other Logistical Fuels

    DOEpatents

    Herling, Darrell R [Richland, WA; Aardahl, Chris L [Richland, WA; Rozmiarek, Robert T [Middleton, WI; Rappe, Kenneth G [Richland, WA; Wang, Yong [Richland, WA; Holladay, Jamelyn D [Kennewick, WA

    2008-10-14

    The present invention provides a process for producing reagents for a chemical reaction by introducing a fuel containing hydrocarbons into a flash distillation process wherein the fuel is separated into a first component having a lower average molecular weight and a second component having a higher average molecular weight. The first component is then reformed to produce synthesis gas wherein the synthesis gas is reacted catalytically to produce the desire reagent.

  12. Method of generating hydrocarbon reagents from diesel, natural gas and other logistical fuels

    DOEpatents

    Herling, Darrell R.; Aardahl, Chris L.; Rozmiarek, Robert T.; Rappe, Kenneth G.; Wang, Yong; Holladay, Jamelyn D.

    2010-06-29

    The present invention provides a process for producing reagents for a chemical reaction by introducing a fuel containing hydrocarbons into a flash distillation process wherein the fuel is separated into a first component having a lower average molecular weight and a second component having a higher average molecular weight. The first component is then reformed to produce synthesis gas wherein the synthesis gas is reacted catalytically to produce the desire reagent.

  13. Prediction of ecotoxicity of hydrocarbon-contaminated soils using physicochemical parameters

    SciTech Connect

    Wong, D.C.L.; Chai, E.Y.; Chu, K.K.; Dorn, P.B.

    1999-11-01

    The physicochemical properties of eight hydrocarbon-contaminated soils were used to predict toxicity to earthworms (Eisenia fetida) and plants. The toxicity of these preremediated soils was assessed using earthworm avoidance, survival, and reproduction and seed germination and root growth in four plant species. No-observed-effect and 25% inhibitory concentrations were determined from the earthworm and plant assays. Physical property measurements and metals analyses of the soils were conducted. Hydrocarbon contamination was characterized by total petroleum hydrocarbons, oil and grease, and GC boiling-point distribution. Univariate and multivariate statistical methods were used to examine relationships between physical and chemical properties and biological endpoints. Soil groupings based on physicochemical properties and toxicity from cluster and principal component analyses were generally similar. Correlation analysis identified a number of significant relationships between soil parameters and toxicity that were used in univariate model development. Total petroleum hydrocarbons by gas chromatography and polars were identified as predictors of earthworm avoidance and survival and seed germination, explaining 65 to 75% of the variation in the data. Asphaltenes also explained 83% of the variation in seed germination. Gravimetric total petroleum hydrocarbons explained 40% of the variation in earthworm reproduction, whereas 43% of the variation in plant root growth was explained by asphaltenes. Multivariate one-component partial least squares models, which identified predictors similar to those identified by the univariate models, were also developed for worm avoidance and survival and seed germination and had predictive powers of 42 and 29%, respectively.

  14. Gravimetric imaging of partially molten bodies beneath the Bolivian Altiplano

    NASA Astrophysics Data System (ADS)

    del Potro, R.; Diez, M.; Gottsmann, J.; Camacho, A. J.; Sunagua, M.

    2011-12-01

    The presence of partial melt in the Earth's crust causes a decrease in density, and hence a density contrast, that generates a potential field anomaly. Gravimetric techniques can quantify such an anomaly and invert its signature to produce a subsurface density distribution model, from which images of anomalous density bodies can be isolated. Here, we present a 3D gravimetric image of four deep-rooted negative density bodies in the Central Volcanic Zone of the Andes in southern Bolivia, which we interpret to contain partial melt. The underlying gravimetric data were obtained by the combination of 143 new with 60 existing observation from previous regional surveys. The survey covers an area of ~5000 km2 that comprises the Central Andean Bouguer anomaly minima of about -450 μGal. After standard data reduction, the local residual gravity signal was inverted using a priori determined plausible density contrasts (±50 to ±300 kg m-3). The inversion routine builds a subsurface model (defined by the 3D aggregation of parallel-piped cells) based on a controlled 'growth' process of anomalous density bodies by means of an exploratory approach. Non-uniqueness is addressed by favouring solutions that balance minimum residuals and minimum number of anomalous bodies with minimum anomalous mass. Within the range of assumed density contrasts, all inversion models show the presence of the deep-rooted low-density bodies, providing a significant confidence level to the inversion results. Our favoured 3D model of the anomalous bodies is obtained from a negative density contrast of 150 kg m-3 that corresponds to <30 vol% partial melt of dacitic composition. These partially molten bodies appear to connect the Altiplano-Puna Magma Body (AMPB) at ~20 km depth, to shallower (~5 km) pre-eruption levels beneath the Altiplano-Puna Volcanic Complex (APVC). One of the bodies is located beneath a large on-going ground uplift centred at Uturuncu volcano and the modelled ground deformation source

  15. Application of solid/liquid extraction for the gravimetric determination of lipids in royal jelly.

    PubMed

    Antinelli, Jean-François; Davico, Renée; Rognone, Catherine; Faucon, Jean-Paul; Lizzani-Cuvelier, Louisette

    2002-04-10

    Gravimetric lipid determination is a major parameter for the characterization and the authentication of royal jelly quality. A solid/liquid extraction was compared to the reference method, which is based on liquid/liquid extraction. The amount of royal jelly and the time of the extraction were optimized in comparison to the reference method. Boiling/rinsing ratio and spread of royal jelly onto the extraction thimble were identified as critical parameters, resulting in good accuracy and precision for the alternative method. Comparison of reproducibility and repeatability of both methods associated with gas chromatographic analysis of the composition of the extracted lipids showed no differences between the two methods. As the intra-laboratory validation tests were comparable to the reference method, while offering rapidity and a decrease in amount of solvent used, it was concluded that the proposed method should be used with no modification of quality criteria and norms established for royal jelly characterization.

  16. Quantitative structure-activity relationship modeling of polycyclic aromatic hydrocarbon mutagenicity by classification methods based on holistic theoretical molecular descriptors.

    PubMed

    Gramatica, Paola; Papa, Ester; Marrocchi, Assunta; Minuti, Lucio; Taticchi, Aldo

    2007-03-01

    Various polycyclic aromatic hydrocarbons (PAHs), ubiquitous environmental pollutants, are recognized mutagens and carcinogens. A homogeneous set of mutagenicity data (TA98 and TA100,+S9) for 32 benzocyclopentaphenanthrenes/chrysenes was modeled by the quantitative structure-activity relationship classification methods k-nearest neighbor and classification and regression tree, using theoretical holistic molecular descriptors. Genetic algorithm provided the selection of the best subset of variables for modeling mutagenicity. The models were validated by leave-one-out and leave-50%-out approaches and have good performance, with sensitivity and specificity ranges of 90-100%. Mutagenicity assessment for these PAHs requires only a few theoretical descriptors of their molecular structure.

  17. Method and apparatus for separating wax/water from hydrocarbon mixture boiling in the lubricating oil range

    SciTech Connect

    Mintz, D.J.; Gleason, A.M.

    1986-04-08

    A method is described of separating wax particles and/or water droplets from a hydrocarbon oil mixture boiling in the lubricating oil range, in which mixture the wax/water forms a dispersion. The free excess electric charge which is net unipolar is introduced into the wax/water-containing oil mixture and the charged wax/water-containing oil mixture and at least one collector surface are brought into contact with one another so that the wax/water collects, due to the electrophoretic migration of the wax/water caused by the introduced electric charge, and accumulates on the collector surface(s).

  18. BOREAS HYD-8 1994 Gravimetric Moss Moisture Data

    NASA Technical Reports Server (NTRS)

    Wang, Xuewen; Hall, Forrest G. (Editor); Knapp, David E. (Editor); Smith, David E. (Technical Monitor)

    2000-01-01

    The Boreal Ecosystem-Atmosphere Study (BOREAS) Hydrology (HYD)-8 team made measurements of surface hydrological processes that were collected at the Northern Study Area-Old Black Spruce (NSA-OBS) Tower Flux site in 1994 and at Joey Lake, Manitoba, to support its research into point hydrological processes and the spatial variation of these processes. The data collected may be useful in characterizing canopy interception, drip, throughfall, moss interception, drainage, evaporation, and capacity during the growing season at daily temporal resolution. This particular data set contains the gravimetric moss moisture measurements from June to September 1994. A nested spatial sampling plan was implemented to support research into spatial variations of the measured hydrological processes and ultimately the impact of these variations on modeled carbon and water budgets. These data are stored in tabular ASCII files. The HYD-08 1994 gravimetric moss moisture data are available from the Earth Observing System Data and Information System (EOSDIS) Oak Ridge National Laboratory (ORNL) Distributed Active Archive Center (DAAC). The data files are available on a CD-ROM (see document number 20010000884).

  19. An approximate method for calculating composition of the non-equilibrium explosion products of hydrocarbons and oxygen

    NASA Astrophysics Data System (ADS)

    Shargatov, V. A.; Gubin, S. A.; Okunev, D. Yu

    2016-09-01

    We develop a method for calculating the changes in composition of the explosion products in the case where the complete chemical equilibrium is absent but the bimolecular reactions are in quasi-equilibrium with the exception bimolecular reactions with one of the components of the mixture. We investigate the possibility of using the method of "quasiequilibrium" for mixtures of hydrocarbons and oxygen. The method is based on the assumption of the existence of the partial chemical equilibrium in the explosion products. Without significant loss of accuracy to the solution of stiff differential equations detailed kinetic mechanism can be replaced by one or two differential equation and a system of algebraic equations. This method is always consistent with the detailed mechanism and can be used separately or in conjunction with the solution of a stiff system for chemically non-equilibrium mixtures replacing it when bimolecular reactions are near to equilibrium.

  20. A principal-component and least-squares method for allocating polycyclic aromatic hydrocarbons in sediment to multiple sources

    SciTech Connect

    Burns, W.A.; Mankiewicz, P.J.; Bence, A.E.; Page, D.S.; Parker, K.R.

    1997-06-01

    A method was developed to allocate polycyclic aromatic hydrocarbons (PAHs) in sediment samples to the PAH sources from which they came. The method uses principal-component analysis to identify possible sources and a least-squares model to find the source mix that gives the best fit of 36 PAH analytes in each sample. The method identified 18 possible PAH sources in a large set of field data collected in Prince William Sound, Alaska, USA, after the 1989 Exxon Valdez oil spill, including diesel oil, diesel soot, spilled crude oil in various weathering states, natural background, creosote, and combustion products from human activities and forest fires. Spill oil was generally found to be a small increment of the natural background in subtidal sediments, whereas combustion products were often the predominant sources for subtidal PAHs near sites of past or present human activity. The method appears to be applicable to other situations, including other spills.

  1. Method for the production of hydrocarbons using iron-carbon-based catalysts

    SciTech Connect

    Rice, G.W.; Fiato, R.A.; Soled, S.L.

    1988-11-29

    This patent describes a process for producing C/sub 2/+ aliphatic hydrocarbons from a CO and H/sub 2/ mixture comprising the step of contacting the mixture with a catalyst comprising finely divided nonpyrophoric iron-carbon catalyst particles comprising iron and carbon, in the substantial absence of silicon, a substantial portion of which is dementite, which was produced in a reaction zone in the presence of laser radiation under such conditions of laser flux density, power adsorption, concentration of iron compound reactants selected from the group consisting of iron carbonyls, iron acetylacetonate, and ferrocene, and pressure sufficient to produce non-pyrophoric iron-carbon particles having average diameters between 1 and 100 nm.

  2. Method for maximizing the pumpability efficiency of a hydrocarbon slurry by controlling the wax crystal content

    SciTech Connect

    Tackett, J.E.

    1982-01-12

    The efficiency of pumping a hydrocarbon slurry in a pipeline is determined prior to transportation by the relationship: delta P AEBX wherein delta P is the pressure drop expected to be experienced by the slurry in the pipeline in pounds per square inch (psi), ''A'' and ''B'' are constants relating to the size of the pipeline, the flow rate of the slurry and the hydrodynamic volume of the wax crystals, and ''X'' is the wax crystal content in the slurry from the congealed particles in percentage by weight. The wax crystal content of the slurry is measured, such as by nuclear magnetic resonance and/or differential scanning calorimetry, and is used in conjunction with the constants ''A'' and ''B'' to determine the expected pressure drop of the slurry in a particular pipeline. The wax crystal content of the slurry may then be modified, if necessary, to obtain desirable or optimum slurry pumpability conditions for the pipeline.

  3. Spectrophotometric, potentiometric, and gravimetric determination of lanthanides with peri-dihydroxynaphthindenone

    SciTech Connect

    Hassan, S.S.M.; Mahmoud, W.H.

    1982-02-01

    Sensitive and reasonably selective methods are described for the spectrophotometric, potentiometric, and gravimetric determination of lanthanides using peri-dihydroxynaphthindenone as a novel chromogenic and precipitating reagent. The reagent forms a stable 1:2 (metal:reagent) type of complex with light lanthanides at pH 2-7 in 1:1 ethanol-water mixture. Low metal concentrations (<10 ..mu..g/mL) develop colored species (lambda/sub max/ 580 to 590 nm, epsilon/sub max/ (4-6) x 10/sup 4/ L mol/sup -1/ cm/sup -1/) which obey Beer's law. Quantitative precipitation of the complexes from metal solutions of concentrations > 100 ..mu..g/mL permits both gravimetric quantitation by igniting the precipitates to the metal oxides and potentiometric titration of the excess reagent. Results with an average recovery of 98% (standard deviation 0.7%) are obtainable for 0.1 ..mu..g to 200 mg of all light lanthanides. Many foreign ions naturally occurring or frequently associated with lanthanides do not interfere or can be tolerated.

  4. Pre-formulation studies on moisture absorption in microcrystalline cellulose using differential thermo-gravimetric analysis.

    PubMed

    Heng, Paul Wan Sia; Liew, Celine Valeria; Soh, Josephine Lay Peng

    2004-04-01

    A study on the differential thermo-gravimetric (DTG) measurements of microcrystalline cellulose (MCC) containing moisture indicated that particle size affected the amount of bound water and the flow indices. Thermal analysis of 6 commercial grades of MCC powders and MCC/water blends were performed using a thermo-gravimetric analyzer. These MCCs were differentiated by their particle size, bulk and tapped densities, crystallinity and micromeritic properties. From the DTG curves, it was observed that water loss from the MCC/water blends occurred in 3 phases which corresponded to the different states of water associated with the solid particles. Area under the third phase, or the falling rate phase, can be associated with the release of water that was physically shielded or bound to the solid. This water may be referred to as "structured" water. The large particle size grades of MCC-Avicel PH 102, PH 302 and Pharmacel 102 were found to possess smaller quantities of structured water. Water vapor sorption results revealed the monolayer capacities for the respective MCC grades. The amount of structured water appeared to correspond to the existence of bilayers on the surface of the small particle size MCC grades. Using the avalanche flow assessment method, flow properties of small particle size grades of MCC were found to be poorer as indicated by the significant correlation between their flow indices and size, in addition to the longer mean times to avalanche.

  5. Determination of soil moisture distribution from impedance and gravimetric measurements

    NASA Technical Reports Server (NTRS)

    Ungar, Stephen G.; Layman, Robert; Campbell, Jeffrey E.; Walsh, John; Mckim, Harlan J.

    1992-01-01

    Daily measurements of the soil dielectric properties at 5 and 10 cm were obtained at five locations throughout the First ISLSCP Field Experiment (FIFE) test site during the 1987 intensive field campaigns (IFCs). An automated vector voltmeter was used to monitor the complex electrical impedance, at 10 MHz, of cylindrical volumes of soil delineated by specially designed soil moisture probes buried at these locations. The objective of this exercise was to test the hypothesis that the soil impedance is sensitive to the moisture content of the soil and that the imaginary part (that is, capacitive reactance) can be used to calculate the volumetric water content of the soil. These measurements were compared with gravimetric samples collected at these locations by the FIFE staff science team.

  6. Non-gravimetric contributions to QCR sensor response.

    PubMed

    Lucklum, Ralf

    2005-11-01

    Quartz crystal resonator (QCR) sensors are commonly known as mass sensitive devices, usually called QCM (Quartz Crystal Microbalance). This constricted view should not be applied to biosensor applications. In many cases the sensor response is strongly influenced or even governed by non-gravimetric effects; the QCR sensor does not act as a microbalance. For better understanding of the sensor response as well as for sensor optimization a more general description of the sensor principle is required. The Transmission Line Model (TLM) is a powerful tool to describe the transduction scheme of QCR and other acoustic-wave based sensors. It is therefore applied to the analysis of the sensor behavior under several conditions, which can be expected in biochemical experiments. The generalization of acoustic parameters provides a concept to overcome some of the limiting assumptions of the present TLM.

  7. BOREAS HYD-6 Ground Gravimetric Soil Moisture Data

    NASA Technical Reports Server (NTRS)

    Carroll, Thomas; Knapp, David E. (Editor); Hall, Forrest G. (Editor); Peck, Eugene L.; Smith, David E. (Technical Monitor)

    2000-01-01

    The Boreal Ecosystem-Atmosphere Study (BOREAS) Hydrology (HYD)-6 team collected several data sets related to the moisture content of soil and overlying humus layers. This data set contains percent soil moisture ground measurements. These data were collected on the ground along the various flight lines flown in the Southern Study Area (SSA) and Northern Study Area (NSA) during 1994 by the gamma ray instrument. The data are available in tabular ASCII files. The HYD-06 ground gravimetric soil moisture data are available from the Earth Observing System Data and Information System (EOSDIS) Oak Ridge National Laboratory (ORNL) Distributed Active Archive Center (DAAC). The data files are available on a CD-ROM (see document number 20010000884).

  8. Evaluation of methods for simultaneous collection and determination of nicotine and polynuclear aromatic hydrocarbons in indoor air

    SciTech Connect

    Chuang, J.C.; Kuhlman, M.R.; Wilson, N.K.

    1990-01-01

    A study was performed to determine whether one sampling system and one analytical method can be used to measure both polynuclear aromatic hydrocarbons (PAH) and nicotine. The PAH collection efficiencies for both XAD-2 and XAD-4 adsorbents are very similar, but the nicotine collection efficiency was greater for XAD-4. The spiked perdeuterated PAH were retained well in both adsorbents after exposure to more than 300 cu m of air. A two-step Soxhlet extraction, dichloromethane followed by ethylacetate, was used to remove nicotine and PAH from XAD-4. The extract was analyzed by positive chemical ionization or electron impact gas chromatography/mass spectrometry (GC/MS) to determine nicotine and PAH. It is shown that one sampling system (quartz fiber filter and XAD-4 in series) and one analytical method (Soxhlet extraction and GC/MS) can be used to measure both nicotine and PAH in indoor air.

  9. Evaluation of methods for simultaneous collection and determination of nicotine and polynuclear aromatic hydrocarbons in indoor air

    SciTech Connect

    Chuang, J.C.; Kuhlman, M.R. ); Wilson, N.K. )

    1990-05-01

    A study was performed to determine whether one sampling system and one analytical method can be used to collect and measure both polynuclear aromatic hydrocarbons (PAHs) and nicotine. PAH collection efficiencies for both XAD-2 and XAD-4 adsorbents were very similar, but nicotine collection efficiency was greater for XAD-4. Spiked perdeuterated PAHs were retained well in both adsorbents after exposure to more than 300 m{sup 3} of air. A two-step Soxhlet extraction, dichloromethane followed by ethyl acetate, was used to remove nicotine and PAHs from XAD-4. The extract was analyzed by positive chemical ionization or electron impact gas chromatography/mass spectrometry (GC/MS) to determine nicotine and PAHs. It is shown that one sampling system (quartz fiber filter and XAD-4 in series) and one analytical method (Soxhlet extraction and GC/MS) can be used for both nicotine and PAHs in indoor.

  10. Gravimetric and spectrophotometric determination of some phenothiazine and imidazole derivatives in coated tablets and tablets.

    PubMed

    Iliaszenko, J; Sokołowska, M; Paruszewski, R

    2001-01-01

    Two drugs in the form of coated tablets: Promazin (promazine hydrochloride) (1) and Thioridazin (thioridazine hydrochloride) (2), and tablets Clotrimazolum (clotrimazole) (3) were assayed gravimetrically and spectrophotometrically in the same process using complexes with ammonium molybdate. Stoichiometry of these complexes was established by elemental analysis and analysis of the incineration residue (MoO3). The complexes were subsequently characterized using their IR and UV spectra and melting points. The active substances of the complexes were also determined spectrophotometrically. Using this method Beers Law was found to hold for the concentration ranges of 5-40 microg/ml (complex of 1), 5-60 (microg/ml (complex of 2) and 2-10 microg/ml (complex of 3). The method was validated in terms of precision, linearity, detection limit and quantification limit. The two methods of drug determination, used in a single analytical process verify each other.

  11. Rapid methods for classification and quantitative assessment of petroleum hydrocarbons pollution in soil samples using reflectance spectroscopy.

    NASA Astrophysics Data System (ADS)

    Schwartz, G.; Eshel, G.; Ben-Haim, M.; Ben-Dor, E.

    2009-04-01

    Petroleum hydrocarbons (PHC) are one of the most significant environmental polluter (for both soil and water) mainly due to its mass production and use (13.26 million cubic meters of crude oil per day). The commonly used method for PHC determination in soil samples is by PHC extraction from the soil sample using 1,1,2-Trichlorotrifluoroethane (Freon 113) and afterwards determining the total PHC (TPH) by FTIR. This method is expensive and time consuming; in addition the use of Freon 113 was recently prohibited by the EPA. Therefore, there is a great need for alternative methods which are environmental friendly and can rapidly detect low concentrations of petroleum hydrocarbon in soils. The adoption of this approach to evaluate PHC contamination in soils is obvious and a few works have partially demonstrated this application. This study focused on using defused spectral analysis across the VNIR-SWIR region (400-2500 nm) to directly determine PHC in soil samples especially at low concentrations. We used artificially contaminated soil samples (diesel and fuel) that were analyzed by both the common method (extraction with Freon 113) and spectrally. Several statistical models were tested for predicting TPH in soils for a large concentration range (100 - 10000 ppm). More than one hundred field contaminated soil samples have been collected and analyzed in the same manner. Preliminary combined generic models are being tested, for in situ use for quantifying TPH in soils at high precisions levels, as well as identifying fuel type in the soil medium with great success. Our results show that PHC contamination in soils can be evaluated generically in situ, rapidly, accurately, and cost effectively.

  12. Critical evaluation of selected methods for the isolation of polycyclic aromatic hydrocarbons from wood stove creosote

    SciTech Connect

    MacDonald, S.J.

    1987-01-01

    The polycyclic aromatic hydrocarbon (PAH) content of creosote samples from a conventional air tight residential wood burning stove and a Franklin type stove were analyzed. It was determined that these samples did contain most of those PAH identified by the Environmental Protection Agency as priority pollutants. Furthermore, it was evidenced that these compounds are present in creosote generated by the air tight stove at levels approximately twice those found in the Franklin type counterpart. The investigation also focused on the evaluation of different classical liquid, and planar chromatographic techniques as well as the introduction of a novel approach for the isolation of PAH material from creosote. It was found that adsorbents commonly employed were too difficult to standardize for routine use and that the cleanest PAH fractions were obtained by gradient elution, circular, thin layer chromatography. Finally, the potential for future applications of gradient elution, circular, thin layer chromatography was demonstrated by the separation of both polar and nonpolar components in a single chromatogram.

  13. Humidity and Gravimetric Equivalency Adjustments for Nephelometer-Based Particulate Matter Measurements of Emissions from Solid Biomass Fuel Use in Cookstoves

    PubMed Central

    Soneja, Sutyajeet; Chen, Chen; Tielsch, James M.; Katz, Joanne; Zeger, Scott L.; Checkley, William; Curriero, Frank C.; Breysse, Patrick N.

    2014-01-01

    Great uncertainty exists around indoor biomass burning exposure-disease relationships due to lack of detailed exposure data in large health outcome studies. Passive nephelometers can be used to estimate high particulate matter (PM) concentrations during cooking in low resource environments. Since passive nephelometers do not have a collection filter they are not subject to sampler overload. Nephelometric concentration readings can be biased due to particle growth in high humid environments and differences in compositional and size dependent aerosol characteristics. This paper explores relative humidity (RH) and gravimetric equivalency adjustment approaches to be used for the pDR-1000 used to assess indoor PM concentrations for a cookstove intervention trial in Nepal. Three approaches to humidity adjustment performed equivalently (similar root mean squared error). For gravimetric conversion, the new linear regression equation with log-transformed variables performed better than the traditional linear equation. In addition, gravimetric conversion equations utilizing a spline or quadratic term were examined. We propose a humidity adjustment equation encompassing the entire RH range instead of adjusting for RH above an arbitrary 60% threshold. Furthermore, we propose new integrated RH and gravimetric conversion methods because they have one response variable (gravimetric PM2.5 concentration), do not contain an RH threshold, and is straightforward. PMID:24950062

  14. Humidity and gravimetric equivalency adjustments for nephelometer-based particulate matter measurements of emissions from solid biomass fuel use in cookstoves.

    PubMed

    Soneja, Sutyajeet; Chen, Chen; Tielsch, James M; Katz, Joanne; Zeger, Scott L; Checkley, William; Curriero, Frank C; Breysse, Patrick N

    2014-06-19

    Great uncertainty exists around indoor biomass burning exposure-disease relationships due to lack of detailed exposure data in large health outcome studies. Passive nephelometers can be used to estimate high particulate matter (PM) concentrations during cooking in low resource environments. Since passive nephelometers do not have a collection filter they are not subject to sampler overload. Nephelometric concentration readings can be biased due to particle growth in high humid environments and differences in compositional and size dependent aerosol characteristics. This paper explores relative humidity (RH) and gravimetric equivalency adjustment approaches to be used for the pDR-1000 used to assess indoor PM concentrations for a cookstove intervention trial in Nepal. Three approaches to humidity adjustment performed equivalently (similar root mean squared error). For gravimetric conversion, the new linear regression equation with log-transformed variables performed better than the traditional linear equation. In addition, gravimetric conversion equations utilizing a spline or quadratic term were examined. We propose a humidity adjustment equation encompassing the entire RH range instead of adjusting for RH above an arbitrary 60% threshold. Furthermore, we propose new integrated RH and gravimetric conversion methods because they have one response variable (gravimetric PM2.5 concentration), do not contain an RH threshold, and is straightforward.

  15. Method and apparatus for determining the presence or absence of a pour point depressant additive in hydrocarbon liquids

    SciTech Connect

    Rummel, J.D.

    1986-07-29

    A method is described of determining the presence or absence of a pour point depressant additive in a hydrocarbon liquid derived from petroleum, the liquid containing paraffin wax, comprising the steps of: (a) cooling a sample of the liquid at a predetermined cooling rate from a temperature substantially above the cloud point temperature to a temperature substantially below the cloud point temperature; (b) monitoring the slope of the cooling rate curve and noting the points at which a deflection in the curve begins and ends; (c) determining the time interval between the beginning and ending points of the deflection of the curve, and (d) comparing the determined time interval to a reference time interval, associated with the predetermined cooling rate, so as to establish whether the determined time interval is less than or greater than the reference time interval thereby establishing the presence or absence, respectively, of a pour point depressant additive.

  16. Method and apparatus for separating wax/water from hydrocarbon oil mixture boiling in the lubricating oil range

    SciTech Connect

    Chimenti, R.J.L.; Cerkanowicz, A.E.; Ryan, D.G.

    1986-11-11

    A method is described of enhancing separation of wax particles and/or water droplets from hydrocarbon oil mixture boiling in the lubricating oil range. In the oil mixture the wax/water forms a dispersion, in which the wax particles and/or water droplets are grown in size, before being separated from the oil mixture. This done by introducing free excess electric charge which is net unipolar into a body of the wax/water-containing oil mixture which is devoid of any collector surfaces disposed inside the body of oil mixture, and by allowing the introduced charge to induce the growth in size of wax particles and/or water droplets within the body of oil mixture.

  17. Availability and leaching of polycyclic aromatic hydrocarbons: Controlling processes and comparison of testing methods.

    PubMed

    Roskam, Gerlinde D; Comans, Rob N J

    2009-01-01

    We have studied the availability and leaching of polycyclic aromatic hydrocarbons (PAHs) from two contaminated materials, a tar-containing asphalt granulate (Sigma16 US-EPA PAHs 3412mg/kg) and gasworks soil (SigmaPAHs 900mg/kg), by comparing results from three typical types of leaching tests: a column, sequential batch, and two different availability tests. The sequential batch test was found to largely resemble the column test. However, the leaching of particularly the larger PAHs (>5 aromatic rings) was found to be enhanced in the batch test by up to an order of magnitude, probably due to their association with large DOC (dissolved organic carbon) molecules generated by the vigorous mixing. The release of PAHs in the two availability tests, in which the leaching is facilitated by either a high concentration of DOC or Tenax resin, was similar, although the latter test was easier to perform and yielded more repeatable results. The availability was much higher than the amount leached in the column and sequential batch tests. However, biodegradation had apparently occurred in the column test and the total amount of PAHs released by either leaching or biodegradation, 9% and 26% for asphalt granulate and gasworks soil, respectively, did equal the amount leached in the availability tests. Therefore, the availability was found to provide a relevant measure of the PAH fraction that can be released from the solid phase. These results stress the importance of using the available instead of the total amount of contaminant in the risk analysis of solid materials in utilization or disposal. PMID:18554897

  18. Gravimetric determination of the continental-oceanic boundary of the Argentine continental margin (from 36°S to 50°S)

    NASA Astrophysics Data System (ADS)

    Arecco, María Alejandra; Ruiz, Francisco; Pizarro, Guillermo; Giménez, Mario; Martínez, Patricia; Ramos, Víctor A.

    2016-01-01

    This paper presents the gravimetric analysis together with seismic data as an integral application in order to identify the continental-oceanic crust boundary (COB) of the Argentine continental margin from 36°S to 50°S in a continuous way. The gravimetric and seismic data are made up of large grids of data obtained from satellite altimetry and marine research. The methodology consists of three distinct methods: (i) the application of enhancement techniques to gravimetric anomalies, (ii) the calculation of crustal thinning from 3-D gravity inversion modelling of the crust-mantle discontinuity and (iii) 2-D gravimetric modelling supported by multichannel reflection and refraction seismic profiles. In the first method, the analytic signal, Theta map, and tilt angle and its horizontal derivative were applied. In the second method, crustal thickness was obtained as the difference in the depths of the crystalline basement and the crust-mantle discontinuity; the latter was obtained via gravimetric inversion. Finally, 2-D modelling was performed from free-air anomalies in two representative sections by considering as restriction surfaces those coming from the interpretation of seismic data. The results of the joint application of enhancement techniques and 2-D and 3-D modelling have enabled continuous interpretation of the COB. In this study, the COB was determined continuously from the integration of 2-D profiles of the enhancement techniques, taking account of crustal thickness and performing 2-D gravimetric modelling. The modelling technique was complemented by regional studies integrated with multichannel seismic reflection and seismic refraction lines, resulting in consistent enhancement techniques.

  19. Evaluation of gravimetric and volumetric dispensers of particles of nuclear material. [Accurate dispensing of fissile and fertile fuel into fuel rods

    SciTech Connect

    Bayne, C.K.; Angelini, P.

    1981-08-01

    Theoretical and experimental studies compared the abilities of volumetric and gravimetric dispensers to dispense accurately fissile and fertile fuel particles. Such devices are being developed for the fabrication of sphere-pac fuel rods for high-temperature gas-cooled light water and fast breeder reactors. The theoretical examination suggests that, although the fuel particles are dispensed more accurately by the gravimetric dispenser, the amount of nuclear material in the fuel particles dispensed by the two methods is not significantly different. The experimental results demonstrated that the volumetric dispenser can dispense both fuel particles and nuclear materials that meet standards for fabricating fuel rods. Performance of the more complex gravimetric dispenser was not significantly better than that of the simple yet accurate volumetric dispenser.

  20. Gravimetric determination of tin with sodium cyclotetramethylenedithiocarbamate and its applications in metal analysis.

    PubMed

    Nan, Z

    1998-08-01

    A gravimetric determination of tin is proposed with sodium cyclotetramethylenedithiocarbamate as precipitant at pH 5.0-5.5. By optimizing the reaction conditions the theoretical conversion factor 0.1687 can be used for determining >/=5% of Sn. Its standard deviation (n=10) at the level of 20 mg of Sn was found to be 0.08 mg. Effects of diverse cationic species can be eliminated by a clear-cut group precipitation at pH 9 with DDTC in the presence of tartrate and subsequent masking with EDTA. Provision is also made for removal of individual species in occasional cases. Hence, the proposed method is flexible and versatile and was successfully applied to the macro-determination of Sn in diverse alloys.

  1. Buoyancy-corrected gravimetric analysis of lightly loaded filters.

    PubMed

    Rasmussen, Pat E; Gardner, H David; Niu, Jianjun

    2010-09-01

    Numerous sources of uncertainty are associated with the gravimetric analysis of lightly loaded air filter samples (< 100 microg). The purpose of the study presented here is to investigate the effectiveness and limitations of air buoyancy corrections over experimentally adjusted conditions of temperature (21-25 degrees C) and relative humidity (RH) (16-60% RH). Conditioning (24 hr) and weighing were performed inside the Archimedes M3 environmentally controlled chamber. The measurements were performed using 20 size-fractionated samples of resuspended house dust loaded onto Teflo (PTFE) filters using a Micro-Orifice Uniform Deposit Impactor representing a wide range of mass loading (7.2-3130 microg) and cut sizes (0.056-9.9 microm). By maintaining tight controls on humidity (within 0.5% RH of control setting) throughout pre- and postweighing at each stepwise increase in RH, it was possible to quantify error due to water absorption: 45% of the total mass change due to water absorption occurred between 16 and 50% RH, and 55% occurred between 50 and 60% RH. The buoyancy corrections ranged from -3.5 to +5.8 microg in magnitude and improved relative standard deviation (RSD) from 21.3% (uncorrected) to 5.6% (corrected) for a 7.2 microg sample. It is recommended that protocols for weighing low-mass particle samples (e.g., nanoparticle samples) should include buoyancy corrections and tight temperature/humidity controls. In some cases, conditioning times longer than 24 hr may be warranted.

  2. Airborne Gravity Data Enhances NGS Experimental Gravimetric Geoid in Alaska

    NASA Astrophysics Data System (ADS)

    Holmes, S. A.; Childers, V. A.; Li, X.; Roman, D. R.

    2014-12-01

    The U.S. National Geodetic Survey [NGS], through their Gravity for the Redefinition of the American Vertical Datum [GRAV-D] program, continues to update its gravimetry holdings by flying new airborne gravity surveys over a large fraction of the USA and its territories. By 2022, NGS intends that all orthometric heights in the USA will be determined in the field by using a reliable national gravimetric geoid model to transform from geodetic heights obtained from GPS. Several airborne campaigns have already been flown over Alaska and its coastline. Some of this Alaskan coastal data have been incorporated into a new NGS experimental geoid model - xGEOID14. The xGEOID14 model is the first in a series of annual experimental geoid models that will incorporate NGS GRAV-D airborne data. This series provides a useful benchmark for assessing and improving current techniques by which the airborne and land-survey data are filtered and cleaned, and then combined with satellite gravity models, elevation data (etc.) with the ultimate aim of computing a geoid model that can support a national physical height system by 2022. Here we will examine the NGS GRAV-D airborne data in Alaska, and assess its contribution to xGEOID14. Future prospects for xGEOID15 will also be considered.

  3. A High Throughput Method for Measuring Polycyclic Aromatic Hydrocarbons in Seafood Using QuEChERS Extraction and SBSE.

    PubMed

    Pfannkoch, Edward A; Stuff, John R; Whitecavage, Jacqueline A; Blevins, John M; Seely, Kathryn A; Moran, Jeffery H

    2015-01-01

    National Oceanic and Atmospheric Administration (NOAA) Method NMFS-NWFSC-59 2004 is currently used to quantitatively analyze seafood for polycyclic aromatic hydrocarbon (PAH) contamination, especially following events such as the Deepwater Horizon oil rig explosion that released millions of barrels of crude oil into the Gulf of Mexico. This method has limited throughput capacity; hence, alternative methods are necessary to meet analytical demands after such events. Stir bar sorptive extraction (SBSE) is an effective technique to extract trace PAHs in water and the quick, easy, cheap, effective, rugged, and safe (QuEChERS) extraction strategy effectively extracts PAHs from complex food matrices. This study uses SBSE to concentrate PAHs and eliminate matrix interference from QuEChERS extracts of seafood, specifically oysters, fish, and shrimp. This method provides acceptable recovery (65-138%) linear calibrations and is sensitive (LOD = 0.02 ppb, LOQ = 0.06 ppb) while providing higher throughput and maintaining equivalency between NOAA 2004 as determined by analysis of NIST SRM 1974b mussel tissue.

  4. A High Throughput Method for Measuring Polycyclic Aromatic Hydrocarbons in Seafood Using QuEChERS Extraction and SBSE

    PubMed Central

    Pfannkoch, Edward A.; Stuff, John R.; Whitecavage, Jacqueline A.; Blevins, John M.; Seely, Kathryn A.; Moran, Jeffery H.

    2015-01-01

    National Oceanic and Atmospheric Administration (NOAA) Method NMFS-NWFSC-59 2004 is currently used to quantitatively analyze seafood for polycyclic aromatic hydrocarbon (PAH) contamination, especially following events such as the Deepwater Horizon oil rig explosion that released millions of barrels of crude oil into the Gulf of Mexico. This method has limited throughput capacity; hence, alternative methods are necessary to meet analytical demands after such events. Stir bar sorptive extraction (SBSE) is an effective technique to extract trace PAHs in water and the quick, easy, cheap, effective, rugged, and safe (QuEChERS) extraction strategy effectively extracts PAHs from complex food matrices. This study uses SBSE to concentrate PAHs and eliminate matrix interference from QuEChERS extracts of seafood, specifically oysters, fish, and shrimp. This method provides acceptable recovery (65–138%) linear calibrations and is sensitive (LOD = 0.02 ppb, LOQ = 0.06 ppb) while providing higher throughput and maintaining equivalency between NOAA 2004 as determined by analysis of NIST SRM 1974b mussel tissue. PMID:25873967

  5. Quantitation of polycyclic aromatic hydrocarbons (PAH4) in cocoa and chocolate samples by an HPLC-FD method.

    PubMed

    Raters, Marion; Matissek, Reinhard

    2014-11-01

    As a consequence of the PAH4 (sum of four different polycyclic aromatic hydrocarbons, named benzo[a]anthracene, chrysene, benzo[b]fluoranthene, and benzo[a]pyrene) maximum levels permitted in cocoa beans and derived products as of 2013, an high-performance liquid chromatography with fluorescence detection method (HPLC-FD) was developed and adapted to the complex cocoa butter matrix to enable a simultaneous determination of PAH4. The resulting analysis method was subsequently successfully validated. This method meets the requirements of Regulation (EU) No. 836/2011 regarding analysis methods criteria for determining PAH4 and is hence most suitable for monitoring the observance of the maximum levels applicable under Regulation (EU) No. 835/2011. Within the scope of this work, a total of 218 samples of raw cocoa, cocoa masses, and cocoa butter from several sample years (1999-2012), of various origins and treatments, as well as cocoa and chocolate products were analyzed for the occurrence of PAH4. In summary, it is noted that the current PAH contamination level of cocoa products can be deemed very slight overall.

  6. A High Throughput Method for Measuring Polycyclic Aromatic Hydrocarbons in Seafood Using QuEChERS Extraction and SBSE.

    PubMed

    Pfannkoch, Edward A; Stuff, John R; Whitecavage, Jacqueline A; Blevins, John M; Seely, Kathryn A; Moran, Jeffery H

    2015-01-01

    National Oceanic and Atmospheric Administration (NOAA) Method NMFS-NWFSC-59 2004 is currently used to quantitatively analyze seafood for polycyclic aromatic hydrocarbon (PAH) contamination, especially following events such as the Deepwater Horizon oil rig explosion that released millions of barrels of crude oil into the Gulf of Mexico. This method has limited throughput capacity; hence, alternative methods are necessary to meet analytical demands after such events. Stir bar sorptive extraction (SBSE) is an effective technique to extract trace PAHs in water and the quick, easy, cheap, effective, rugged, and safe (QuEChERS) extraction strategy effectively extracts PAHs from complex food matrices. This study uses SBSE to concentrate PAHs and eliminate matrix interference from QuEChERS extracts of seafood, specifically oysters, fish, and shrimp. This method provides acceptable recovery (65-138%) linear calibrations and is sensitive (LOD = 0.02 ppb, LOQ = 0.06 ppb) while providing higher throughput and maintaining equivalency between NOAA 2004 as determined by analysis of NIST SRM 1974b mussel tissue. PMID:25873967

  7. Determination of volatile organic and polycyclic aromatic hydrocarbons in crude oil with efficient gas-chromatographic methods.

    PubMed

    Wang, Haijing; Geppert, Helmut; Fischer, Thomas; Wieprecht, Wolfgang; Möller, Detlev

    2015-01-01

    Determination of volatile organic compounds (VOCs) in crude oil, such as super volatile organic compounds (super VOCs) and simple polycyclic aromatic hydrocarbons (PAHs), is vital for targeting crude oil spill spots. In this study, a static headspace gas chromatography flame ionization detection method was established for determination of super VOCs in crude oil with both external and internal standard determination, which can be used in the field when using portable gas chromatography. Identification was done by comparing the retention time with the corresponding standards and quantitation was done with a new one-drop method. Another simplified and efficient method was performed to analyze volatile PAHs in crude oil, which can also be used in field analysis. Toluene was used as the extraction solvent for PAHs in crude oil. Method validation for both analyses was satisfactory. The result showed that n-butane and n-pentane were maximum super VOCs and naphthalene, phenanthrene and fluorene were the main PAHs in the crude oil studied. The super VOCs quantity ranged from 3 to 6% and the main PAHs consisted of 0.02-0.06% of studied crude oil. PMID:25225200

  8. Quantification and interpretation of total petroleum hydrocarbons in sediment samples by a GC/MS method and comparison with EPA 418.1 and a rapid field method.

    PubMed

    Xie, G; Barcelona, M J; Fang, J

    1999-05-01

    Total petroleum hydrocarbons (TPH) as a lumped parameter can be easily and rapidly measured or monitored. Despite interpretational problems, it has become an accepted regulatory benchmark used widely to evaluate the extent of petroleum product contamination. Three currently used methods (GC/MS, conventional EPA 418.1, and a rapid field method PetroFLAG) were performed to quantify the TPH content in samples collected from a site contaminated by transformer oil. To standardize the method and improve the comparability of TPH data, crucial GC-based quantification issues were examined, e.g., quantification based on internal standards (ISTD) vs external standards (ESTD), single vs multiple ISTD, and various area integration approaches. The interpretation of hydrocarbon chromatographic results was examined in the context of field samples. The performance of the GC/MS method was compared with those of EPA 418.1 and PetroFLAG. As a result, it was observed that the ISTD quantification method was preferred to the ESTD method, multiple ISTD might be better than single ISTD, and three different area integration approaches did not have a significant effect on TPH results. Evaluation of the chromatograms between a reference sample and three unknown samples showed that the extent of contamination varied appreciably with sample depth. It was also found that there existed a good positive correlation between GC/MS and both EPA 418.1 and PetroFLAG, and that EPA 418.1 produced the higher overall estimate while GC/MS and PetroFLAG resulted in lower, more statistically comparable TPH values.

  9. Gravimetric preparation and characterization of primary reference solutions of molybdenum and rhodium.

    PubMed

    Kaltenbach, Angela; Noordmann, Janine; Görlitz, Volker; Pape, Carola; Richter, Silke; Kipphardt, Heinrich; Kopp, Gernot; Jährling, Reinhard; Rienitz, Olaf; Güttler, Bernd

    2015-04-01

    Gravimetrically prepared mono-elemental reference solutions having a well-known mass fraction of approximately 1 g/kg (or a mass concentration of 1 g/L) define the very basis of virtually all measurements in inorganic analysis. Serving as the starting materials of all standard/calibration solutions, they link virtually all measurements of inorganic analytes (regardless of the method applied) to the purity of the solid materials (high-purity metals or salts) they were prepared from. In case these solid materials are characterized comprehensively with respect to their purity, this link also establishes direct metrological traceability to The International System of Units (SI). This, in turn, ensures the comparability of all results on the highest level achievable. Several national metrology institutes (NMIs) and designated institutes (DIs) have been working for nearly two decades in close cooperation with commercial producers on making an increasing number of traceable reference solutions available. Besides the comprehensive characterization of the solid starting materials, dissolving them both loss-free and completely under strict gravimetric control is a challenging problem in the case of several elements like molybdenum and rhodium. Within the framework of the European Metrology Research Programme (EMRP), in the Joint Research Project (JRP) called SIB09 Primary standards for challenging elements, reference solutions of molybdenum and rhodium were prepared directly from the respective metals with a relative expanded uncertainty associated with the mass fraction of U rel(w) < 0.05 %. To achieve this, a microwave-assisted digestion procedure for Rh and a hotplate digestion procedure for Mo were developed along with highly accurate and precise inductively coupled plasma optical emission spectrometry (ICP OES) and multicollector inductively coupled plasma mass spectrometry (MC-ICP-MS) methods required to assist with the preparation and as dissemination tools.

  10. Magnetic solid phase extraction and static headspace gas chromatography-mass spectrometry method for the analysis of polycyclic aromatic hydrocarbons.

    PubMed

    Cai, Ying; Yan, Zhihong; Wang, Lijia; NguyenVan, Manh; Cai, Qingyun

    2016-01-15

    A magnetic solid phase extraction (MSPE) protocol combining a static headspace gas chromatography coupled to mass spectrometry (HS-GC-MS) method has been developed for extraction, and determination of 16 polycyclic aromatic hydrocarbons (PAHs) in drinking water samples. Magnetic nanoparticles (MNPs) were coated with 3-aminopropyltriethoxysilane and modified by cholesterol chloroformate. Transmission electron microscope, vibrating sample magnetometer, Fourier transform infrared spectrometry and X-ray photoelectron spectroscopy were used to characterize the cholesterol-functionalized sorbents, and the main parameters affecting the extraction as well as HS sampling, such as sorbent amount, extraction time, oven temperature and equilibration time have been investigated and established. Combination with HS sampling, the MSPE procedure was simple, fast and environmentally friendly, without need of any organic solvent. Method validation proved the feasibility of the developed sorbents for the quantitation of the investigated analytes at trace levels obtaining the limit of detection (S/N=3) ranging from 0.20 to 7.8 ng/L. Good values for intra and inter-day precision were obtained (RSDs ≤ 9.9%). The proposed method was successfully applied to drinking water samples.

  11. The development and evaluation of a gravimetric reference scale for measurements of atmospheric carbon monoxide

    NASA Astrophysics Data System (ADS)

    Novelli, Paul C.; Elkins, James W.; Steele, L. Paul

    1991-07-01

    We have prepared a set of 17 carbon monoxide (CO) reference mixtures for use in the calibration of measurements of atmospheric concentrations of this gas. The mixing ratios of these standards range from 25 to 1003 ppb (parts per billion by mole fraction) in zero natural air and are contained in 5.9-L, high-pressure aluminum cylinders. Carbon monoxide was measured using gas chromatography with a mercuric oxide detector. The concentration range of the standards is sufficient to cover that of the background troposphere and also that found in remote locations affected by anthropogenic activities. The low concentration standards were prepared by gravimetric methods using one of three high concentration standards as the parent. Two of the parents were prepared by gravimetric methods starting from high-purity (99.97%) CO to have concentrations of about 250 ppm (parts per million) CO. A total of 14 atmospheric level primary standards were prepared from these two parents. The third parent was a NIST SRM (National Institute of Standards and Technology, Standard Reference Material) having 9.7 ppm CO, from which three standards were prepared. Monitoring of CO levels in the primary standards, relative to natural air contained in 29.5-L high-pressure aluminum cylinders, suggests that the CO content of some primaries may be increasing at rates of between 1 and 2 ppb yr-1. The CO concentration scale defined by the gravimetric standards was used to calibrate a set of 10 secondary standards. The secondary standards are all contained in 29.5-L high-pressure aluminum cylinders and range in concentration from 35 to 200 ppb. Examination of the CO content in several of the oldest secondary standards indicates their CO concentrations have not changed relative to each other over the 2 years they have been studied. Comparison of the low concentration standards derived from the gravimetric parents to those prepared from the NIST SRM show no difference to within 1% between the two scales. We

  12. The use of inverse gas chromatography and gravimetric vapour sorption to study transitions in amorphous lactose.

    PubMed

    Ambarkhane, Ameet V; Pincott, Kim; Buckton, Graham

    2005-04-27

    The aim of this study was to measure the glass transition of amorphous lactose under well-controlled temperature and humidity, using inverse gas chromatography (IGC) and to relate these data to gravimetric vapour sorption experiments. Amorphous lactose (spray-dried) was exposed to a stepwise increment in the relative humidity (%RH) under isothermal conditions in an IGC. At the end of each conditioning step a decane injection was made, and the retention volumes were calculated using the maximum peak height (V(max)) method. The pressure drop across the column was recorded using the pressure transducers. These measurements were performed at various temperatures from 25 to 40 degrees C. The extent of water sorption at identical humidity (%RH) and temperature conditions was determined gravimetrically using dynamic vapour sorption (DVS). At each T, it was possible to determine: (1) a transition at low RH relating to the onset of mobility; (2) changes in retention volume relating to the point, where T(g) = T; (3) changes in pressure drop, which were related to the sample collapse. The rate and extent of water sorption was seen to alter at T(g) and also at a collapse point. Combinations of temperature and critical %RH (%cRH required to lower the dry glass transition temperature to the experimental temperature) obtained from IGC were comparable to those obtained from DVS. It was shown that at each T, the sample spontaneously crystallised, when T(g) was 32 degrees C below T. Inverse gas chromatograph can be used in this novel way to reveal the series of transitions that occur in amorphous materials.

  13. Remote detection of hydrocarbon seeps

    SciTech Connect

    Barringer, A. R.

    1985-05-14

    A method of detecting hydrocarbon seeps in a sea or in earth is disclosed. The method involves interrogating aerosols formed above the sea or earth surface with an intense beam of primary light radiation generated aboard an aircraft or other vehicle. The spectral composition of the beam is selected to induce secondary light radiation in certain hydrocarbon materials contained in aerosols generated by hydrocarbon seeps rising to the sea or earth surface. The secondary light radiation is detected aboard the aircraft and subjected to spectral analysis to determine whether the composition of the aerosols is characteristic of aerosols generated by hydrocarbon seeps. Apparatus for implementing the method is also disclosed.

  14. Multifunctional nanoparticles as simulants for a gravimetric immunoassay.

    PubMed

    Miller, Scott A; Hiatt, Leslie A; Keil, Robert G; Wright, David W; Cliffel, David E

    2011-01-01

    Immunoassays are important tools for the rapid detection and identification of pathogens, both clinically and in the research laboratory. An immunoassay with the potential for the detection of influenza was developed and tested using hemagglutinin (HA), a commonly studied glycoprotein found on the surface of influenza virions. Gold nanoparticles were synthesized, which present multiple peptide epitopes, including the HA epitope, in order to increase the gravimetric response achieved with the use of a QCM immunosensor for influenza. Specifically, epitopes associated with HA and FLAG peptides were affixed to gold nanoparticles by a six-mer PEG spacer between the epitope and the terminal cysteine. The PEG spacer was shown to enhance the probability for interaction with antibodies by increasing the distance the epitope extends from the gold surface. These nanoparticles were characterized using thermogravimetric analysis, transmission electron microscopy, matrix-assisted laser desorption/ionization-time of flight, and (1)H nuclear magnetic resonance analysis. Anti-FLAG and anti-HA antibodies were adhered to the surface of a QCM, and the response of each antibody upon exposure to HA, FLAG, and dual functionalized nanoparticles was compared with binding of Au-tiopronin nanoparticles and H5 HA proteins from influenza virus (H5N1). Results demonstrate that the immunoassay was capable of differentiating between nanoparticles presenting orthogonal epitopes in real-time with minimal nonspecific binding. The detection of H5 HA protein demonstrates the logical extension of using these nanoparticle mimics as a safe positive control in the detection of influenza, making this a vital step in improving influenza detection methodology.

  15. Oil and gas exploration system and method for detecting trace amounts of hydrocarbon gases in the atmosphere

    DOEpatents

    Wamsley, Paula R.; Weimer, Carl S.; Nelson, Loren D.; O'Brien, Martin J.

    2003-01-01

    An oil and gas exploration system and method for land and airborne operations, the system and method used for locating subsurface hydrocarbon deposits based upon a remote detection of trace amounts of gases in the atmosphere. The detection of one or more target gases in the atmosphere is used to indicate a possible subsurface oil and gas deposit. By mapping a plurality of gas targets over a selected survey area, the survey area can be analyzed for measurable concentration anomalies. The anomalies are interpreted along with other exploration data to evaluate the value of an underground deposit. The system includes a differential absorption lidar (DIAL) system with a spectroscopic grade laser light and a light detector. The laser light is continuously tunable in a mid-infrared range, 2 to 5 micrometers, for choosing appropriate wavelengths to measure different gases and avoid absorption bands of interference gases. The laser light has sufficient optical energy to measure atmospheric concentrations of a gas over a path as long as a mile and greater. The detection of the gas is based on optical absorption measurements at specific wavelengths in the open atmosphere. Light that is detected using the light detector contains an absorption signature acquired as the light travels through the atmosphere from the laser source and back to the light detector. The absorption signature of each gas is processed and then analyzed to determine if a potential anomaly exists.

  16. An empirical method for calculating the viscosities of hydrocarbon liquids and liquid mixtures

    SciTech Connect

    Peng, D.Y.; Vermani, R.

    1987-01-01

    The viscosities of pure liquid normal alkanes ranging from propane to n-tetradecane are correlated using the Peng-Robinson equation of state in conjunction with Hildebrand's empirical theory of fluidity. A mixing rule and an excess fluidity function are proposed. Simulated viscosity data generated from the corresponding states method of Ely and Hanley are used to determine the binary interaction parameters needed in the excess function which has its form based on the Wilson equation. The procedure has been used to calculate the viscosities of binary mixtures and simulated multicomponent liquid n-alkane mixtures involving the above-mentioned components at temperatures to 444 K and pressures to 200 bar. The results are compared with the predicted values obtained from the corresponding states method. The procedure is simple to use and it has an accuracy comparable to that of the theoretically based but more elaborate method.

  17. A novel and cost-effective method for the determination of fifteen polycyclic aromatic hydrocarbons in low volume rainwater samples.

    PubMed

    Fernández-Amado, M; Prieto-Blanco, M C; López-Mahía, P; Muniategui-Lorenzo, S; Prada-Rodríguez, D

    2016-08-01

    A novel single-step method was developed for the determination of 15 polycyclic aromatic hydrocarbons (PAHs) at ultratrace levels in rainwater by on-line in-tube solid-phase microextraction (IT-SPME) coupled to high-performance liquid chromatography-photodiode array-fluorescence detection. This paper is focused on a study of the IT-SPME coupling and optimization, its application to rainwater and other environmental waters and the stability of PAH rainwater solutions. In order to solve the different extractive behavior of PAHs, several IT-SPME parameters were optimized, with the type and percentage of organic modifier playing a decisive role. In the kinetic study on stability of PAH solutions, the organic modifier has proven to be effective as a preservative, avoiding the loss of the higher-molecular weight PAHs. The proposed method presents a wide interval of linearity (10-1500ngL(-1)) and a good relative standard deviation between 3.4% and 14.6% for the PAHs analyzed. Detection and quantification limits between 2.3 and 28ngL(-1) and 5.7 and 65ngL(-1) were obtained respectively, taking into account the values of the procedure blanks. Recoveries for different kinds of real water samples were within the range of 72-110%. Low and medium-molecular weight PAHs predominate in daily and monthly rainwater samples analyzed. In comparison with other methods reported, the proposed method achieves a significant reduction of the sample volume, the organic solvent consumption and time of sample treatment, allowing a cost-effective analysis of environmental waters. The method is especially suitable for samples from the precipitation events of low intensity or short duration for which sample volume is limiting. PMID:27216671

  18. Comparison of photoacoustic radiometry to gas chromatography/mass spectrometry methods for monitoring chlorinated hydrocarbons

    SciTech Connect

    Sollid, J.E.; Trujillo, V.L.; Limback, S.P.; Woloshun, K.A.

    1996-03-01

    A comparison of two methods of gas chromatography mass spectrometry (GCMS) and a nondispersive infrared technique, photoacoustic radiometry (PAR), is presented in the context of field monitoring a disposal site. First is presented an historical account describing the site and early monitoring to provide an overview. The intent and nature of the monitoring program changed when it was proposed to expand the Radiological Waste Site close to the Hazardous Waste Site. Both the sampling methods and analysis techniques were refined in the course of this exercise.

  19. DELINEATION OF SUBSURFACE HYDROCARBON CONTAMINANT DISTRIBUTION USING A DIRECT PUSH RESISTIVITY METHOD

    EPA Science Inventory

    A direct push resistivity method was evaluated as a complementary screening tool to provide rapid in-situ contaminant detection to aid in better defining locations for drilling, sampling, and monitoring well installation at hazardous waste sites. Nine continuous direct push resi...

  20. System and method for controlling hydrogen elimination during carbon nanotube synthesis from hydrocarbons

    DOEpatents

    Reilly, Peter T. A.

    2010-03-23

    A system and method for producing carbon nanotubes by chemical vapor deposition includes a catalyst support having first and second surfaces. The catalyst support is capable of hydrogen transport from the first to the second surface. A catalyst is provided on the first surface of the catalyst support. The catalyst is selected to catalyze the chemical vapor deposition formation of carbon nanotubes. A fuel source is provided for supplying fuel to the catalyst.

  1. Evaluation of Chemical Analysis Method and Determination of Polycyclic Aromatic Hydrocarbons Content from Seafood and Dairy Products

    PubMed Central

    Lee, So-Young; Lee, Jee-Yeon

    2015-01-01

    This study was carried out to investigate contents of 8 polycyclic aromatic hydrocarbons (PAHs) from frequently consumed seafood and dairy products and to evaluate their chemical analysis methods. Samples were collected from markets of 9 cities in Korea chosen as the population reference and evaluated. The methodology involved saponification, extraction with n-hexane, clean-up on Sep-Pak silica cartridges and gas chromatograph-mass spectrometry analysis. Validation proceeded on 2 matrices. Recoveries for 8 PAHs ranged from 86.87 to 103.57%. The limit of detection (LOD) 8 PAHs was 0.04~0.20 µg/kg, and limit of quantification (LOQ) of 8 PAHs was 0.12~0.60 µg/kg. The mean concentration of benzo[a]pyrene (BaP) was 0.34 µg/kg from seafood and 0.34 µg/kg from dairy products. The total PAHs concentration was 1.06 µg/kg in seafood and 1.52 µg/kg in dairy products. PMID:26483885

  2. Evaluation of field methods for estimating exposure of children in low-income families to polycyclic aromatic hydrocarbons

    SciTech Connect

    Wilson, N.K.; Chuang, J.C.; Lyu, C.

    1996-12-31

    Children in low-income families may have higher exposures to polycyclic aromatic hydrocarbons (PAH) and related compounds than children in higher-income families. These higher exposures could result from the location of their homes, nearer to industrial sites and traffic; from poorer diet; from environmental tobacco smoke; or other causes. The study was designed to evaluate methods and estimate the range of total exposures of low-income children to PAH through various pathways. Nonsmoking participants with preschool children, incomes at or below the official US poverty level, and space heating in their homes were recruited. The PAH concentrations were measured in the household indoor and outdoor air, house dust, and yard soil, and in the diet of both an adult and a preschool child living in the home. An initial study in two homes and an additional study of nine homes, four urban and five rural, during the heating season were completed. The problems and successes encountered in the recruitment process and selected results of the heating season measurements are summarized in the paper.

  3. Studies on the dissolution of polycyclic aromatic hydrocarbons from contaminated materials using a novel dialysis tubing experimental method

    SciTech Connect

    Woolgar, P.J. Scottish Environment Protection Agency, Stirling ); Jones, K.C. )

    1999-06-15

    Assessment of risk and remediation strategies at contaminated sites requires that both the amounts of contaminants present and their potential for release from materials and soils be evaluated. The release, or dissolution, of polycyclic aromatic hydrocarbons (PAHs) from contaminated materials to water was therefore investigated. To facilitate investigations of PAH dissolution from physically disparate materials such as solid coal tars, creosote, oil, and spent oxide, an experimental method for measuring dissolved PAHs was developed employing dialysis tubing in batch-type system. This was validated and compared to aqueous-phase PAH concentrations measured using more traditional techniques and also predicted using Raoult's law. The experimental procedure was successfully used to determine near equilibrium aqueous concentrations of PAHs, but it could only be used to determine relative rates of approach to equilibrium as the dialysis tubing effected the rate constants. It was found that the contaminant materials influenced dissolution, in particular the close to equilibrium concentrations. For materials chemically similar to PAHs, such as nonaqueous-phase liquids (NAPLs), the concentrations could be predicted using Raoult's law. For materials that were chemically dissimilar to PAHs, such as spent oxide, release was more thermodynamically favorable than for NAPLs.

  4. Identifying sources of chlorinated aliphatic hydrocarbons in a residential area in Italy using the integral pumping test method

    NASA Astrophysics Data System (ADS)

    Alberti, Luca; Lombi, Silvia; Zanini, Andrea

    2011-09-01

    The results of integral pumping tests (IPTs) performed in the city of Fabriano, Italy, are presented. The IPT methodology was developed by the European Union project INCORE, as a tool for groundwater investigation and source localization in contaminated areas. This methodology consists of a multiple-well pumping test in which the wells are positioned along a control plane downstream of suspected contaminant source zones and perpendicular to the mean groundwater flow direction. During the pumping, concentration time series of target contaminants are measured. In Fabriano, two control planes were realized to identify a chlorinated aliphatic hydrocarbon plume, to estimate the mass fluxes and draw up a ranked list of the main contamination sources. A numerical flow model was implemented to support the IPT design and to interpret the results. This study revealed low-level trichloroethylene contamination (concentration below 8 μg/l), tetrachloroethylene contamination (mean concentration up to 500 μg/l) and a mass flow rate of about 300 g/day. Through the application of the IPT method, the mean contaminant concentrations, the spatial distribution of concentration values along the control planes, and the total contaminant mass flow rates were evaluated, and the investigation area was reduced for further and deeper investigation activities.

  5. The potential of solvent-minimized extraction methods in the determination of polycyclic aromatic hydrocarbons in fish oils.

    PubMed

    Yebra-Pimentel, Iria; Martínez-Carballo, Elena; Regueiro, Jorge; Simal-Gándara, Jesús

    2013-08-15

    Fish oil has been identified as one of the most important contributors to the level of Persistent Organic Pollutants (POPs) in feed products. The determination of polycyclic aromatic hydrocarbons (PAHs) in fish oils is complicated due to the fat matrix, which affects both extraction efficiency and analytical quality. This article reviews and addresses two of the most relevant analytical methods for determining 11 mutagenic and carcinogenic PAHs, as well as two EPA indicator PAHs in fish oils. We discuss and critically evaluate two different extraction procedures, such as ultrasound-assisted solvent extraction (USAE) and ultrasound-assisted emulsification-microextraction (USAEME). Clean-up of extracts was performed by solid-phase extraction using C18 and glass columns containing silica gel and florisil for USAE or only C18 for USAEME. Detection of the selected PAHs was carried out by high-performance liquid chromatography coupled with fluorescence detection for determination. Optimization of the variables affecting extraction by the selected extraction techniques was conducted and recoveries ranged from 70% to 100% by USAE and from 70% to 108% by USAEME with estimated quantification limits between 0.020 and 2.6 μg/kg were achieved. Moreover, the applicability of the selected methods was evaluated by the analysis of real samples. To our knowledge, this is the first time that USAEME has been applied to the determination of PAHs in food matrices, such as oil fish samples. The methods proposed were applied to the determination of the target PAHs in fish samples from different countries, and it was found that the low PAH contamination of the selected fish oils could mainly occur by atmospheric sources. PMID:23561207

  6. The potential of solvent-minimized extraction methods in the determination of polycyclic aromatic hydrocarbons in fish oils.

    PubMed

    Yebra-Pimentel, Iria; Martínez-Carballo, Elena; Regueiro, Jorge; Simal-Gándara, Jesús

    2013-08-15

    Fish oil has been identified as one of the most important contributors to the level of Persistent Organic Pollutants (POPs) in feed products. The determination of polycyclic aromatic hydrocarbons (PAHs) in fish oils is complicated due to the fat matrix, which affects both extraction efficiency and analytical quality. This article reviews and addresses two of the most relevant analytical methods for determining 11 mutagenic and carcinogenic PAHs, as well as two EPA indicator PAHs in fish oils. We discuss and critically evaluate two different extraction procedures, such as ultrasound-assisted solvent extraction (USAE) and ultrasound-assisted emulsification-microextraction (USAEME). Clean-up of extracts was performed by solid-phase extraction using C18 and glass columns containing silica gel and florisil for USAE or only C18 for USAEME. Detection of the selected PAHs was carried out by high-performance liquid chromatography coupled with fluorescence detection for determination. Optimization of the variables affecting extraction by the selected extraction techniques was conducted and recoveries ranged from 70% to 100% by USAE and from 70% to 108% by USAEME with estimated quantification limits between 0.020 and 2.6 μg/kg were achieved. Moreover, the applicability of the selected methods was evaluated by the analysis of real samples. To our knowledge, this is the first time that USAEME has been applied to the determination of PAHs in food matrices, such as oil fish samples. The methods proposed were applied to the determination of the target PAHs in fish samples from different countries, and it was found that the low PAH contamination of the selected fish oils could mainly occur by atmospheric sources.

  7. Method for recovery of hydrocarbons form contaminated soil or refuse materials

    DOEpatents

    Ignasiak, Teresa; Turak, Ali A.; Pawlak, Wanda; Ignasiak, Boleslaw L.; Guerra, Carlos R.; Zwillenberg, Melvin L.

    1991-01-01

    A method is provided for separating an inert solid substantially inorganic fraction comprising sand or soil from a tarry or oily organic matter in a feedstock. The feedstock may be contaminated soil or tarry waste. The feedstock is combined with pulverized coal and water. The ratio (oil or tar to dry weight of coal) of about 1.0:10 to about 4.0:10 at a temperature in the range of 60.degree.-95.degree. C. The mixture is agitated, the coarse particles are removed, and up to about 0.10% by weight (based on weight of coal) of a frothing agent is added. The mixture is then subjected to flotation, and the froth is removed from the mixture.

  8. Decontamination of produced water containing petroleum hydrocarbons by electrochemical methods: a minireview.

    PubMed

    dos Santos, Elisama Vieira; Bezerra Rocha, Jessica Horacina; de Araújo, Danyelle Medeiros; de Moura, Dayanne Chianca; Martínez-Huitle, Carlos Alberto

    2014-01-01

    Produced water (PW) is the largest waste stream generated in oil and gas industries. The drilling and extraction operations that are aimed to maximize the production of oil may be counterbalanced by the huge production of contaminated water (called PW) with pollutants, such as heavy metals, dissolved/suspended solids, and organic compounds. PW is conventionally treated through different physical, chemical, and biological methods. In offshore platforms, because of space constraints, compact physical and chemical systems are used. However, major research efforts are being developed with innovative technologies for treating PW in order to comply with reuse and discharge limits. Among them, electrochemical technologies have been proposed as a promising alternative for the treatment of this kind of wastewaters. Then, this paper presents a minireview of efficient electrochemical technologies used until now for treating PW generated by petrochemical industry.

  9. Decontamination of produced water containing petroleum hydrocarbons by electrochemical methods: a minireview.

    PubMed

    dos Santos, Elisama Vieira; Bezerra Rocha, Jessica Horacina; de Araújo, Danyelle Medeiros; de Moura, Dayanne Chianca; Martínez-Huitle, Carlos Alberto

    2014-01-01

    Produced water (PW) is the largest waste stream generated in oil and gas industries. The drilling and extraction operations that are aimed to maximize the production of oil may be counterbalanced by the huge production of contaminated water (called PW) with pollutants, such as heavy metals, dissolved/suspended solids, and organic compounds. PW is conventionally treated through different physical, chemical, and biological methods. In offshore platforms, because of space constraints, compact physical and chemical systems are used. However, major research efforts are being developed with innovative technologies for treating PW in order to comply with reuse and discharge limits. Among them, electrochemical technologies have been proposed as a promising alternative for the treatment of this kind of wastewaters. Then, this paper presents a minireview of efficient electrochemical technologies used until now for treating PW generated by petrochemical industry. PMID:24671399

  10. Physically constrained source apportionment (PCSA) for polycyclic aromatic hydrocarbon using the Multilinear Engine 2-species ratios (ME2-SR) method.

    PubMed

    Liu, Gui-Rong; Shi, Guo-Liang; Tian, Ying-Ze; Wang, Yi-Nan; Zhang, Cai-Yan; Feng, Yin-Chang

    2015-01-01

    An improved physically constrained source apportionment (PCSA) technology using the Multilinear Engine 2-species ratios (ME2-SR) method was proposed and applied to quantify the sources of PM10- and PM2.5-associated polycyclic aromatic hydrocarbons (PAHs) from Chengdu in winter time. Sixteen priority PAH compounds were detected with mean ΣPAH concentrations (sum of 16 PAHs) ranging from 70.65 ng/m(3) to 209.58 ng/m(3) and from 59.17 ng/m(3) to 170.64 ng/m(3) for the PM10 and PM2.5 samples, respectively. The ME2-SR and positive matrix factorization (PMF) models were employed to estimate the source contributions of PAHs, and these estimates agreed with the experimental results. For the PMF model, the highest contributor to the ΣPAHs was vehicular emission (81.69% for PM10, 82.06% for PM2.5), followed by coal combustion (12.68%, 12.11%), wood combustion (5.65%, 4.45%) and oil combustion (0.72%, 0.88%). For the ME2-SR method, the highest contributions were from diesel (43.19% for PM10, 47.17% for PM2.5) and gasoline exhaust (34.94%, 32.44%), followed by wood combustion (8.79%, 6.37%), coal combustion (12.46%, 12.37%) and oil combustion (0.80%, 1.22%). However, the PAH ratios calculated for the factors extracted by ME2-SR were closer to the values from actual source profiles, implying that the results obtained from ME2-SR might be physically constrained and satisfactory. PMID:25240101

  11. Physically constrained source apportionment (PCSA) for polycyclic aromatic hydrocarbon using the Multilinear Engine 2-species ratios (ME2-SR) method.

    PubMed

    Liu, Gui-Rong; Shi, Guo-Liang; Tian, Ying-Ze; Wang, Yi-Nan; Zhang, Cai-Yan; Feng, Yin-Chang

    2015-01-01

    An improved physically constrained source apportionment (PCSA) technology using the Multilinear Engine 2-species ratios (ME2-SR) method was proposed and applied to quantify the sources of PM10- and PM2.5-associated polycyclic aromatic hydrocarbons (PAHs) from Chengdu in winter time. Sixteen priority PAH compounds were detected with mean ΣPAH concentrations (sum of 16 PAHs) ranging from 70.65 ng/m(3) to 209.58 ng/m(3) and from 59.17 ng/m(3) to 170.64 ng/m(3) for the PM10 and PM2.5 samples, respectively. The ME2-SR and positive matrix factorization (PMF) models were employed to estimate the source contributions of PAHs, and these estimates agreed with the experimental results. For the PMF model, the highest contributor to the ΣPAHs was vehicular emission (81.69% for PM10, 82.06% for PM2.5), followed by coal combustion (12.68%, 12.11%), wood combustion (5.65%, 4.45%) and oil combustion (0.72%, 0.88%). For the ME2-SR method, the highest contributions were from diesel (43.19% for PM10, 47.17% for PM2.5) and gasoline exhaust (34.94%, 32.44%), followed by wood combustion (8.79%, 6.37%), coal combustion (12.46%, 12.37%) and oil combustion (0.80%, 1.22%). However, the PAH ratios calculated for the factors extracted by ME2-SR were closer to the values from actual source profiles, implying that the results obtained from ME2-SR might be physically constrained and satisfactory.

  12. Reservoir structures detection and hydrocarbons exploration using wavelet transform method in 2 oil fields in southwestern of Iran

    NASA Astrophysics Data System (ADS)

    Hassani, H.; Saadatinejad, M. R.

    2012-04-01

    reservoirs and differ for limestone and sandstone. In this way, CWT applied on vertical sections and in 4 different iso-frequency displaying. By comparing these figures at 10, 16, 24 and 32 Hz, the presence of low frequency shadows under reservoir could be seen. These shadows have distinctly different dynamic frequency responses rather than the background, probably because the hydrocarbons have changed the reflectivity of the reservoir as the anomalies at 10 Hz are bright. In the 16 Hz section, anomalies almost stand out, and the difference between them becomes relatively weak; yet, some of them are still brighter than other anomalies at higher frequencies. Consequently, these variations of anomalies at different frequencies can consider as indicator from presence of hydrocarbons in the target reservoir. Finally, selecting a suitable wavelet is important step of CWT method and in all mentioned usages, Morlet wavelet has beneficial properties to applying in our investigation. In fact, Morlet wavelet demonstrates velocity dispersion and energy absorption to identify fault and gas respectively.

  13. THE PHOTOTOXICITY OF POLYCYCLIC AROMATIC HYDROCARBONS

    EPA Science Inventory

    The U.S. Environmental Protection Agency (EPA) continues to be interested in developing methods for the detection of polycyclic aromatic hydrocarbons (PAHS) in the environment. Polycyclic aromatic hydrocarbons (PAHS) are common contaminants in our environment. Being major product...

  14. International Comparison of FTIR measurements traceable to HITRAN and Gravimetrically prepared Gas Standards

    NASA Astrophysics Data System (ADS)

    Edgar, F.; Joële, V.; Philippe, M.; Faraz, I.; Robert, W.

    2009-12-01

    gas standards and to the molecular data base HITRAN version 2004. Reference values for the comparison will be developed by the BIPM based on gravimetric mixtures prepared from the BIPM’s Primary NO2 facility. The BIPM NO2 facility realises a source of primary reference mixtures and a primary calibration method that combines gravimetry with the dynamic generation of gas mixtures. The primary reference mixtures are prepared and used virtually simultaneously, so stability problems are diminished. The BIPM NO2 facility facilitates the comparison of dynamically generated mixtures with static NO2 mixtures contained in high pressure cylinders which have been used as transfer standards for the comparison. The assigned BIPM NO2 value for each cylinder will be equal to the value predicted from a calibration line calculated from a set of dynamic NO2 primary gas mixtures obtained from the BIPM Nitrogen Dioxide (NO2) Primary Facility where two independent analytical methods, based on ultraviolet spectrophotometry and Fourier Transform Infrared spectroscopy are used for the assignment procedure. This will allow the comparability of HITRAN traceable measurements in over ten different laboratories to be compared to gravimetrically determined values.

  15. First Release of Gravimetric Geoid Model over Saudi Arabia Based on Terrestrial Gravity and GOCE Satellite Data: KSAG01

    NASA Astrophysics Data System (ADS)

    Alothman, Abdulaziz; Elsaka, Basem

    2016-04-01

    A new gravimetric quasi-geoid, known as KSAG0, has been developed recently by Remove-Compute-Restore techniques (RCR), provided by the GRAVSOFT software, using gravimetric free air anomalies. The terrestrial gravity data used in this computations are: 1145 gravity field anomalies observed by ARAMCO (Saudi Arabian Oil Company) and 2470 Gravity measurements from BGI (Bureau Gravimétrique International). The computations were carried out implementing the least squares collocation method through the RCR techniques. The KSAG01 is based on merging in addition to the terrestrial gravity observations, GOCE satellite model (Eigen-6C4) and global gravity model (EGM2008) have been utilized in the computations. The long, medium and short wavelength spectrum of the height anomalies were compensated from Eigen-6C4 and EGM2008 geoid models truncated up to Degree and order (d/o) up to 2190. KSAG01 geoid covers 100 per cent of the kingdom, with geoid heights range from - 37.513 m in the southeast to 23.183 m in the northwest of the country. The accuracy of the geoid is governed by the accuracy, distribution, and spacing of the observations. The standard deviation of the predicted geoid heights is 0.115 m, with maximum errors of about 0.612 m. The RMS of geoid noise ranges from 0.019 m to 0.04 m. Comparison of the predicted gravimetric geoid with EGM, GOCE, and GPS/Levelling geoids, reveals a considerable improvements of the quasi-geoid heights over Saudi Arabia.

  16. Supercritical fluid extraction of fat from ground beef: effects of water on gravimetric and GC-FAME fat determinations.

    PubMed

    Eller, F J; King, J W

    2001-10-01

    This study investigated the supercritical carbon dioxide (SC-CO(2)) extraction of fat from ground beef and the effects of several factors on the gravimetric determination of fat. The use of ethanol modifier with the SC-CO(2) was not necessary for efficient fat extraction; however, the ethanol did increase the coextraction of water. This coextraction of water caused a significant overestimation of gravimetric fat. Oven-drying ground beef samples prior to extraction inhibited the subsequent extraction of fat, whereas oven-drying the extract after collection decreased the subsequent gas chromatographic fatty acid methyl ester (GC-FAME) fat determination. None of the drying agents tested were able to completely prevent the coextraction of water, and silica gel and molecular sieves inhibited the complete extraction of fat. Measurements of collection vial mass indicated that CO(2) extraction/collection causes an initial increase in mass due to the density of CO(2) (relative to displaced air) followed by a decrease in vial mass due to the removal of adsorbed water from the collection vial. Microwave-drying of the empty collection vials removes approximately 3 mg of adsorbed water, approximately 15-20 min is required for readsorption of the displaced water. For collection vials containing collected fat, microwave-drying effectively removed coextracted water, and the vials reached equilibration after approximately 10-15 min. Silanizing collection vials did not significantly affect weight loss during microwave-drying. SC-CO(2) can be used to accurately determine fat gravimetrically for ground beef, and the presented method can also be followed by GC-FAME analysis to provide specific fatty acid information as well.

  17. Occupational exposure to polycyclic aromatic hydrocarbons in airborne particulate matter: validation and application of a gas chromatography-mass spectrometry analytical method.

    PubMed

    Fioretti, Marzia; Catrambone, Tamara; Gordiani, Andrea; Cabella, Renato

    2010-12-01

    This study concerns the validation of an analytical method for the measurement of occupational exposure to trace levels of polycyclic aromatic hydrocarbons (PAHs) in airborne particulate matter (APM). Personal exposure to selected PAHs of five workers occupationally exposed to urban pollution in Rome, Italy, was evaluated. The samples were collected over 10 days evenly distributed during winter and summer of 2008. Polycyclic aromatic hydrocarbons were collected by a sampling pump and trapped in polytetrafluoroethylene filters; ultrasonic extraction was applied to extract PAH species from the matrix with toluene, and the concentrated extract was quantitatively analyzed by GC/MS. The analytical method was optimized and validated using a standard reference material of urban dust (SRM 1649a). Detection limits ranged from 0.8 ng per sample for indeno [1,2,3-cd] pyrene to 20.4 ng for sample for anthracene. Experimental results of the 50 personal samples collected showed that phenanthrene was the predominant polycyclic aromatic hydrocarbon [95% CI (32.42-41.13 ng m(-3))]; the highest benzo[a]pyrene concentration was 2.58 ng m(-3), approximately 2-fold higher than European annual target values (1 ng m(-3)). Seasonal variations of personal exposure to selected PAHs suggested higher emissions and reduced atmospheric reactivity of PAH compounds in winter. The analytical method was a suitable procedure for the determination of 13 of the 16 priority PAHs in APM personal samples and can be considered a useful tool to evaluate occupational exposure to low PAH levels.

  18. The development of a method for the qualitative and quantitative determination of petroleum hydrocarbon components using thin-layer chromatography with flame ionization detection.

    PubMed

    Wang, Shijie; Guo, Guanlin; Yan, Zengguang; Lu, Guilan; Wang, Qunhui; Li, Fasheng

    2010-01-15

    An analytical scheme to determine groups of petroleum hydrocarbon compounds in crude oil was developed and used for the qualitative and quantitative characterization of crude oil samples from the Shengli oilfield, the second largest oilfield in China. Crude oil samples were fractionated and analyzed by thin-layer chromatography with flame ionization detection (TLC-FID). Relative standard deviation (RSD) values for retention time, peak height and half peak width were less than 5.2% for all classes of compounds, based on nine independent replicates. The crude oil light fraction was further analyzed by GC-MS and the majority of identified compounds were methyl- or hydro-derivatives of long-chain hydrocarbons and aromatic compounds. The external standard method used in the present study can lower detection limits of petroleum hydrocarbon compound classes to 20.0 mg L(-1), and the crude oil concentration in the range of 30 and 35,000 mg L(-1) has a high linear correlation (r(2)>0.97, P<0.05) with peak area. A comparison between elution chromatography (EC) and TLC-FID regarding the recovery of petroleum hydrocarbon compounds was carried out with aged crude oil contaminated soils of 50, 80, 200 and 300 mg g(-1). The tested TLC-FID method showed a 10% higher recovery for total extractable materials than the reference EC method. The calibration factor was fraction-dependent and varied with the recovery rate of TLC/EC. Regarding the tested extraction procedures, accelerated solvent extraction (ASE) had a higher extraction efficiency for crude oil contaminated soils than Soxhlet and ultrasonic extractions.

  19. THE APPLICATION OF COMPUTATIONAL MOLECULAR METHODS TO UNDERSTAND THE HEALTH EFFECTS OF ENVIRONMENTAL CHEMICALS-POLYCYCLIC AROMATIC HYDROCARBONS

    EPA Science Inventory

    In evaluating the risk posed by chemicals introduced into the environment, information
    about their molecular mechanism of action provides a basis for extrapolating from the
    laboratory to the environment. Polycyclic aromatic hydrocarbons (PAH) are a large class
    of...

  20. Integration of Remotely-Sensed Geobotanical and Structural Methods for Hydrocarbon Exploration in West-Central West Virginia

    SciTech Connect

    1997-01-26

    This report covers the first of the two years covered in the DOE grant to investigate structural and geobotanical features of hydrocarbon reservoirs in western West Virginia. The reader is referred to the three previous Quarterly reports for greater detail on tasks originally described in those reports. The progress of the project will be discussed with reference to the tasks identified for the project.

  1. QUANTIFICATION AND INTERPRETATION OF TOTAL PETROLEUM HYDROCARBONS IN SEDIMENT SAMPLES BY A GC/MS METHOD AND COMPARISON WITH EPA 418.1 AND A RAPID FIELD METHOD

    EPA Science Inventory

    ABSTRACT: Total Petroleum hydrocarbons (TPH) as a lumped parameter can be easily and rapidly measured or monitored. Despite interpretational problems, it has become an accepted regulatory benchmark used widely to evaluate the extent of petroleum product contamination. Three cu...

  2. Application of real-time PCR, DGGE fingerprinting, and culture-based method to evaluate the effectiveness of intrinsic bioremediation on the control of petroleum-hydrocarbon plume.

    PubMed

    Kao, Chih-Ming; Chen, Colin S; Tsa, Fu-Yu; Yang, Kai-Hsing; Chien, Chih-Ching; Liang, Shih-Hsiung; Yang, Chin-an; Chen, Ssu Ching

    2010-06-15

    Real-time polymerase chain reaction (PCR), denaturing gradient gel electrophoresis (DGGE), and the culture-based method were applied in the intrinsic bioremediation study at a petroleum-hydrocarbon contaminated site. The genes of phenol hydroxylase (PHE), ring-hydroxylating toluene monooxygenase (RMO), naphthalene dioxygenase (NAH), toluene monooxygenase (TOL), toluene dioxygenase (TOD), and biphenyl dioxygenase (BPH4) were quantified by real-time PCR. Results show that PHE gene was detected in groundwater contaminated with benzene, toluene, ethylbenzene, xylene isomers (BTEX) and methyl tert-butyl ether (MTBE), and this indicates that intrinsic bioremediation occurred at this contaminated site. Results from DGGE analyses reveal that the petroleum-hydrocarbon plume caused the variation in microbial communities. In this study, MTBE degraders including Pseudomonas sp. NKNU01, Bacillus sp. NKNU01, Klebsiella sp. NKNU01, Enterobacter sp. NKNU01, and Enterobacter sp. NKNU02 were isolated from the contaminated groundwater using the cultured-based method. Results from MTBE biodegradation experiment show that the isolated bacteria were affected by propane. This indicates that propane may influence the metabolic pathway of MTBE by these bacteria. Knowledge and comprehension obtained from this study will be helpful in evaluating the occurrence and effectiveness of intrinsic bioremediation on the remediation of petroleum-hydrocarbon contaminated groundwater.

  3. Polynuclear aromatic hydrocarbons for fullerene synthesis in flames

    DOEpatents

    Alford, J. Michael; Diener, Michael D.

    2006-12-19

    This invention provides improved methods for combustion synthesis of carbon nanomaterials, including fullerenes, employing multiple-ring aromatic hydrocarbon fuels selected for high carbon conversion to extractable fullerenes. The multiple-ring aromatic hydrocarbon fuels include those that contain polynuclear aromatic hydrocarbons. More specifically, multiple-ring aromatic hydrocarbon fuels contain a substantial amount of indene, methylnapthalenes or mixtures thereof. Coal tar and petroleum distillate fractions provide low cost hydrocarbon fuels containing polynuclear aromatic hydrocarbons, including without limitation, indene, methylnapthalenes or mixtures thereof.

  4. Advanced Nanoporous Materials for Micro-Gravimetric Sensing to Trace-Level Bio/Chemical Molecules

    PubMed Central

    Xu, Pengcheng; Li, Xinxin; Yu, Haitao; Xu, Tiegang

    2014-01-01

    Functionalized nanoporous materials have been developed recently as bio/chemical sensing materials. Due to the huge specific surface of the nano-materials for molecular adsorption, high hopes have been placed on gravimetric detection with micro/nano resonant cantilevers for ultra-sensitive sensing of low-concentration bio/chemical substances. In order to enhance selectivity of the gravimetric resonant sensors to the target molecules, it is crucial to modify specific groups onto the pore-surface of the nano-materials. By loading the nanoporous sensing material onto the desired region of the mass-type transducers like resonant cantilevers, the micro-gravimetric bio/chemical sensors can be formed. Recently, such micro-gravimetric bio/chemical sensors have been successfully applied for rapid or on-the-spot detection of various bio/chemical molecules at the trace-concentration level. The applicable nanoporous sensing materials include mesoporous silica, zeolite, nanoporous graphene oxide (GO) and so on. This review article focuses on the recent achievements in design, preparation, functionalization and characterization of advanced nanoporous sensing materials for micro-gravimetric bio/chemical sensing. PMID:25313499

  5. Advanced nanoporous materials for micro-gravimetric sensing to trace-level bio/chemical molecules.

    PubMed

    Xu, Pengcheng; Li, Xinxin; Yu, Haitao; Xu, Tiegang

    2014-10-13

    Functionalized nanoporous materials have been developed recently as bio/chemical sensing materials. Due to the huge specific surface of the nano-materials for molecular adsorption, high hopes have been placed on gravimetric detection with micro/nano resonant cantilevers for ultra-sensitive sensing of low-concentration bio/chemical substances. In order to enhance selectivity of the gravimetric resonant sensors to the target molecules, it is crucial to modify specific groups onto the pore-surface of the nano-materials. By loading the nanoporous sensing material onto the desired region of the mass-type transducers like resonant cantilevers, the micro-gravimetric bio/chemical sensors can be formed. Recently, such micro-gravimetric bio/chemical sensors have been successfully applied for rapid or on-the-spot detection of various bio/chemical molecules at the trace-concentration level. The applicable nanoporous sensing materials include mesoporous silica, zeolite, nanoporous graphene oxide (GO) and so on. This review article focuses on the recent achievements in design, preparation, functionalization and characterization of advanced nanoporous sensing materials for micro-gravimetric bio/chemical sensing.

  6. Measurement of isotope abundance variations in nature by gravimetric spiking isotope dilution analysis (GS-IDA).

    PubMed

    Chew, Gina; Walczyk, Thomas

    2013-04-01

    Subtle variations in the isotopic composition of elements carry unique information about physical and chemical processes in nature and are now exploited widely in diverse areas of research. Reliable measurement of natural isotope abundance variations is among the biggest challenges in inorganic mass spectrometry as they are highly sensitive to methodological bias. For decades, double spiking of the sample with a mix of two stable isotopes has been considered the reference technique for measuring such variations both by multicollector-inductively coupled plasma mass spectrometry (MC-ICPMS) and multicollector-thermal ionization mass spectrometry (MC-TIMS). However, this technique can only be applied to elements having at least four stable isotopes. Here we present a novel approach that requires measurement of three isotope signals only and which is more robust than the conventional double spiking technique. This became possible by gravimetric mixing of the sample with an isotopic spike in different proportions and by applying principles of isotope dilution for data analysis (GS-IDA). The potential and principle use of the technique is demonstrated for Mg in human urine using MC-TIMS for isotopic analysis. Mg is an element inaccessible to double spiking methods as it consists of three stable isotopes only and shows great potential for metabolically induced isotope effects waiting to be explored.

  7. Acetoxylation of unsaturated hydrocarbons

    SciTech Connect

    Vekki, A.V. de

    1994-06-10

    Acetoxylation is a method for one-step introduction of ester groups into molecules of unsaturated hydrocarbons. Subsequent processing of esters formed may allow an easy preparation of alkanediols and dicarboxylic and polyfunctional carboxylic acids with the required number of carbon atoms.

  8. Phase II Interim Report -- Assessment of Hydrocarbon Seepage Detection Methods on the Fort Peck Reservation, Northeast Montana

    SciTech Connect

    Monson, Lawrence M.

    2002-04-24

    The following work was performed: (1) collected reconnaissance micro-magnetic data and background field data for Area 1, (2) identified and collected soil sample data in three anomalous regions of Area 1, (3) sampled soils in Northwest Poplar Oil Field, (4) graphed, mapped, and interpreted all data areas listed above, (5) registered for the AAPG Penrose Conference on Hydrocarbon Seepage Mechanisms and Migration (postponed from 9/16/01 until 4/7/02 in Vancouver, B.C.). Results include the identification and confirmation of an oil and gas prospect in the northwest part of Area 1 and the verification of a potential shallow gas prospect in the West Poplar Area. Correlation of hydrocarbon micro-seepage to TM tonal anomalies needs further data analysis.

  9. Gravity effects obtained from global hydrology models in comparison with high precision gravimetric time series

    NASA Astrophysics Data System (ADS)

    Wziontek, Hartmut; Wilmes, Herbert; Güntner, Andreas; Creutzfeldt, Benjamin

    2010-05-01

    Water mass changes are a major source of variations in residual gravimetric time series obtained from the combination of observations with superconducting and absolute gravimeters. Changes in the local water storage are the main influence, but global variations contribute to the signal significantly. For three European gravity stations, Bad Homburg, Wettzell and Medicina, different global hydrology models are compared. The influence of topographic effects is discussed and due to the long-term stability of the combined gravity time series, inter-annual signals in model data and gravimetric observations are compared. Two sources of influence are discriminated, i.e., the effect of a local zone with an extent of a few kilometers around the gravimetric station and the global contribution beyond 50km. Considering their coarse resolution and uncertainties, local effects calculated from global hydrological models are compared with the in-situ gravity observations and, for the station Wettzell, with local hydrological monitoring data.

  10. Process for recovering hydrocarbons from a hydrocarbon-bearing formation

    SciTech Connect

    Alston, R.B.; Braden, W.B.; Flournoy, K.H.

    1980-03-11

    A method is described for transporting heavy crude oil through a pipeline which involves introducing into a pipeline or well-bore with the viscous hydrocarbons an aqueous solution containing (1) a sulfonate surfactant, (2) a rosin soap or a naphthenic acid soap and, optionally (3) coupling agent whereby there is spontaneously formed a low viscosity, salt tolerant, oil-in-water emulsion. Also disclosed is a method of recovery of hydrocarbons from a hydrocarbon bearing formation employing an aqueous solution containing (1) a sulfonate surfactant, (2) a rosin soap or a naphthenic acid soap and, optionally (3) a coupling agent.

  11. What is the weighing form in gravimetric determination of antimony(III) with oxine?

    PubMed

    Hioki, Akiharu

    2004-03-01

    The gravimetric analysis of antimony(III) with oxine (8-quinolinol, Hox) was studied. The amount of antimony left in filtrate and washing solutions was corrected with the results of atomic absorption spectrometry. The weighing form, which had not been conclusive before the present study, was determined to be SbO(ox)(Hox)2. The result (purity of antimony(II) oxide: 99.84 +/- 0.05% (m/m)) of the gravimetric analysis was in good agreement with that of coulometric titration with electrogenerated iodine.

  12. High-precision gravimetric coulometry using the silver-perchloric acid coulometer: Titration of arsenious oxide with electrogenerated iodine.

    PubMed

    Newton, C M

    1977-06-01

    High-precision gravimetric coulometry with a silver-perchloric acid coulometer is evaluated as an alternative to the conventional titrimetric method. The loss of weight (caused by electrolytic dissolution) of a highly pure silver anode in series with the cathode of a conventional constant-current titration system is measured and related to the number of equivalents of substance titrated. The precision of the method is determined by titrations of the Standard Reference Material 83C arsenious oxide (99.99% pure) with electrogenerated iodine, using biamperometric end-point detection. Depending on the size of the sample, an ultimate precision of 25 ppm is obtained. The assay for 0.5-g samples of the SRM material is 99.993(9) +/- 0.002(5)% purity.

  13. Gravimetric Analysis of Bismuth in Bismuth Subsalicylate Tablets: A Versatile Quantitative Experiment for Undergraduate Laboratories

    ERIC Educational Resources Information Center

    Davis, Eric; Cheung, Ken; Pauls, Steve; Dick, Jonathan; Roth, Elijah; Zalewski, Nicole; Veldhuizen, Christopher; Coeler, Joel

    2015-01-01

    In this laboratory experiment, lower- and upper-division students dissolved bismuth subsalicylate tablets in acid and precipitated the resultant Bi[superscript 3+] in solution with sodium phosphate for a gravimetric determination of bismuth subsalicylate in the tablets. With a labeled concentration of 262 mg/tablet, the combined data from three…

  14. Comparing Gravimetric and Real-Time Sampling of PM2.5 Concentrations Inside Truck Cabins

    PubMed Central

    Zhu, Ying; Smith, Thomas J.; Davis, Mary E.; Levy, Jonathan I.; Herrick, Robert; Jiang, Hongyu

    2012-01-01

    As part of a study on truck drivers’ exposure and health risk, pickup and delivery (P&D) truck drivers’ on-road exposure patterns to PM2.5 were assessed in five weeklong sampling trips in metropolitan areas of five U.S. cities from April to August of 2006. Drivers were sampled with real-time (DustTrak) and gravimetric samplers to measure average in-cabin PM2.5 concentrations and to compare their correspondence in moving trucks. In addition, GPS measurements of truck locations, meteorological data, and driver behavioral data were collected throughout the day to determine which factors influence the relationship between real-time and gravimetric samplers. Results indicate that the association between average real-time and gravimetric PM2.5 measurements on moving trucks was fairly consistent (Spearman rank correlation of 0.63), with DustTrak measurements exceeding gravimetric measurements by approximately a factor of 2. This ratio differed significantly only between the industrial Midwest cities and the other three sampled cities scattered in the South and West. There was also limited evidence of an effect of truck age. Filter samples collected concurrently with DustTrak measurements can be used to calibrate average mass concentration responses for the DustTrak, allowing for real-time measurements to be integrated into longer-term studies of inter-city and intra-urban exposure patterns for truck drivers. PMID:21991940

  15. Comparing gravimetric and real-time sampling of PM(2.5) concentrations inside truck cabins.

    PubMed

    Zhu, Ying; Smith, Thomas J; Davis, Mary E; Levy, Jonathan I; Herrick, Robert; Jiang, Hongyu

    2011-11-01

    As part of a study on truck drivers' exposure and health risk, pickup and delivery (P&D) truck drivers' on-road exposure patterns to PM(2.5) were assessed in five, weeklong sampling trips in metropolitan areas of five U.S. cities from April to August of 2006. Drivers were sampled with real-time (DustTrak) and gravimetric samplers to measure average in-cabin PM(2.5) concentrations and to compare their correspondence in moving trucks. In addition, GPS measurements of truck locations, meteorological data, and driver behavioral data were collected throughout the day to determine which factors influence the relationship between real-time and gravimetric samplers. Results indicate that the association between average real-time and gravimetric PM(2.5) measurements on moving trucks was fairly consistent (Spearman rank correlation of 0.63), with DustTrak measurements exceeding gravimetric measurements by approximately a factor of 2. This ratio differed significantly only between the industrial Midwest cities and the other three sampled cities scattered in the South and West. There was also limited evidence of an effect of truck age. Filter samples collected concurrently with DustTrak measurements can be used to calibrate average mass concentration responses for the DustTrak, allowing for real-time measurements to be integrated into longer-term studies of inter-city and intra-urban exposure patterns for truck drivers.

  16. Gravimetric excitation function of polar motion from the GRACE RL05 solution

    NASA Astrophysics Data System (ADS)

    Nastula, Y.

    2014-12-01

    Impact of land hydrosphere on polar motion excitation is still not as well known as the impact of the angular momentum of the atmosphere and ocean. Satellite mission Gravity Recovery and Climate Experiment (GRACE) from 2002 provides additional information about mass distribution of the land hydrosphere. However, despite the use of similar computational procedures, the differences between GRACE data series made available by the various centers of computations are still considerable. In the paper we compare three series of gravimetric excitation functions of polar motion determined from Rl05 GRACE solution from the Center for Space Research (CSR), the Jet Propulsion Laboratory (JPL) and the GeoForschungsZentrum (GFZ). These data are used to determine the gravimetric polar motion excitation function. Gravimetric signal is compared also with the geodetic residuals computed by subtracting atmospheric and oceanic signals from geodetic excitation functions of polar motion. Gravimetric excitation functions obtained on the basis of JPL data differ significantly from the geodetic residuals while and the series obtained from CSR and GFZ are more compatible.

  17. On-chip temperature-compensated Love mode surface acoustic wave device for gravimetric sensing

    NASA Astrophysics Data System (ADS)

    Liu, Q.; Flewitt, A. J.

    2014-11-01

    Love mode surface acoustic wave (SAW) sensors have been recognized as one of the most sensitive devices for gravimetric sensors in liquid environments such as bio sensors. Device operation is based upon measuring changes in the transmitted (S21) frequency and phase of the first-order Love wave resonance associated with the device upon on attachment of mass. However, temperature variations also cause a change in the first order S21 parameters. In this work, shallow grooved reflectors and a "dotted" single phase unidirectional interdigitated transducer (D-SPUDT) have been added to the basic SAW structure, which promote unidirectional Love wave propagation from the device's input interdigitated transducers. Not only does this enhance the first-order S21 signal but also it allows propagation of a third-order Love wave. The attenuation coefficient of the third-order wave is sufficiently great that, whilst there is a clear reflected S11 signal, the third-order wave does not propagate into the gravimetric sensing area of the device. As a result, whilst the third-order S11 signal is affected by temperature changes, it is unaffected by mass attachment in the sensing area. It is shown that this signal can be used to remove temperature effects from the first-order S21 signal in real time. This allows gravimetric sensing to take place in an environment without the need for any other temperature measurement or temperature control; this is a particular requirement of gravimetric biosensors.

  18. Geopotential coefficient determination and the gravimetric boundary value problem: A new approach

    NASA Technical Reports Server (NTRS)

    Sjoeberg, Lars E.

    1989-01-01

    New integral formulas to determine geopotential coefficients from terrestrial gravity and satellite altimetry data are given. The formulas are based on the integration of data over the non-spherical surface of the Earth. The effect of the topography to low degrees and orders of coefficients is estimated numerically. Formulas for the solution of the gravimetric boundary value problem are derived.

  19. A combined approach of physicochemical and biological methods for the characterization of petroleum hydrocarbon-contaminated soil.

    PubMed

    Masakorala, Kanaji; Yao, Jun; Chandankere, Radhika; Liu, Haijun; Liu, Wenjuan; Cai, Minmin; Choi, Martin M F

    2014-01-01

    Main physicochemical and microbiological parameters of collected petroleum-contaminated soils with different degrees of contamination from DaGang oil field (southeast of Tianjin, northeast China) were comparatively analyzed in order to assess the influence of petroleum contaminants on the physicochemical and microbiological properties of soil. An integration of microcalorimetric technique with urease enzyme analysis was used with the aim to assess a general status of soil metabolism and the potential availability of nitrogen nutrient in soils stressed by petroleum-derived contaminants. The total petroleum hydrocarbon (TPH) content of contaminated soils varied from 752.3 to 29,114 mg kg(−1). Although the studied physicochemical and biological parameters showed variations dependent on TPH content, the correlation matrix showed also highly significant correlation coefficients among parameters, suggesting their utility in describing a complex matrix such as soil even in the presence of a high level of contaminants. The microcalorimetric measures gave evidence of microbial adaptation under highest TPH concentration; this would help in assessing the potential of a polluted soil to promote self-degradation of oil-derived hydrocarbon under natural or assisted remediation. The results highlighted the importance of the application of combined approach in the study of those parameters driving the soil amelioration and bioremediation.

  20. Synergistic improvement of gas sensing performance by micro-gravimetrically extracted kinetic/thermodynamic parameters.

    PubMed

    Guo, Shuanbao; Xu, Pengcheng; Yu, Haitao; Cheng, Zhenxing; Li, Xinxin

    2015-03-10

    A novel method is explored for comprehensive design/optimization of organophosphorus sensing material, which is loaded on mass-type microcantilever sensor. Conventionally, by directly observing the gas sensing response, it is difficult to build quantitative relationship with the intrinsic structure of the material. To break through this difficulty, resonant cantilever is employed as gravimetric tool to implement molecule adsorption experiment. Based on the sensing data, key kinetic/thermodynamic parameters of the material to the molecule, including adsorption heat -ΔH°, adsorption/desorption rate constants Ka and Kd, active-site number per unit mass N' and surface coverage θ, can be quantitatively extracted according to physical-chemistry theories. With gaseous DMMP (simulant of organophosphorus agents) as sensing target, the optimization route for three sensing materials is successfully demonstrated. Firstly, a hyper-branched polymer is evaluated. Though suffering low sensitivity due to insufficient N', the bis(4-hydroxyphenyl)-hexafluoropropane (BHPF) sensing-group exhibits satisfactory reproducibility due to appropriate -ΔH°. To achieve more sensing-sites, KIT-5 mesoporous-silica with higher surface-area is assessed, resulting in good sensitivity but too high -ΔH° that brings poor repeatability. After comprehensive consideration, the confirmed BHPF sensing-group is grafted on the KIT-5 carrier to form an optimized DMMP sensing nanomaterial. Experimental results indicate that, featuring appropriate kinetic/thermodynamic parameters of -ΔH°, Ka, Kd, N' and θ, the BHPF-functionalized KIT-5 mesoporous silica exhibits synergistic improvement among reproducibility, sensitivity and response/recovery speed. The optimized material shows complete signal recovery, 55% sensitivity improvement than the hyper-branched polymer and 2∼3 folds faster response/recovery speed than the KIT-5 mesoporous silica.

  1. Gravimetric measurements of materials outgassing applied to graphite-epoxy laminates

    NASA Technical Reports Server (NTRS)

    Scialdone, John J.

    1989-01-01

    The outgassing rates of two graphite-epoxy laminates, American Cyanamide 985B-626 and HST-7B-112, were obtained using a gravimetric method. The rates as a function of time and temperature were derived from the measurements of their mass losses at temperatures varying from 25 to 150 C and for a time span of up to 400 hours in a vacuum. The data from those measurements were reduced to obtain the outgassing activation energies, the mass losses per unit mass or area, and the corresponding outgassing rates. The rates are expressed in closed-form equations and are directly usable for medling computations. The procedures to obtain these parameters are shown and may be used for the evaluation of other materials. The results of the tests show that the activation energies of the two materials are: 4630 cal/mole for the 985B-626 materials and 4791 cal/mole for the HST-7B-112 sample no. 10 Graphite Exoxy. The outgassing rates of these materials are in the 10E-5 g/sq cm/hr range and they decay according to a power of time of 0.60 at 25 C, indicating that the outgassing process is mainly a diffusion at that temperature. The normalized mass losses versus time obtained from these tests were compared to the discrete results obtained from the ASTM-E595 tests. The comparison provides general indications on the effects of temperature and time in relation to the ASTM test values obtained at 125 C for a 24-hour test duration.

  2. Development, optimization, validation and application of faster gas chromatography - flame ionization detector method for the analysis of total petroleum hydrocarbons in contaminated soils.

    PubMed

    Zubair, Abdulrazaq; Pappoe, Michael; James, Lesley A; Hawboldt, Kelly

    2015-12-18

    This paper presents an important new approach to improving the timeliness of Total Petroleum Hydrocarbon (TPH) analysis in the soil by Gas Chromatography - Flame Ionization Detector (GC-FID) using the CCME Canada-Wide Standard reference method. The Canada-Wide Standard (CWS) method is used for the analysis of petroleum hydrocarbon compounds across Canada. However, inter-laboratory application of this method for the analysis of TPH in the soil has often shown considerable variability in the results. This could be due, in part, to the different gas chromatography (GC) conditions, other steps involved in the method, as well as the soil properties. In addition, there are differences in the interpretation of the GC results, which impacts the determination of the effectiveness of remediation at hydrocarbon-contaminated sites. In this work, multivariate experimental design approach was used to develop and validate the analytical method for a faster quantitative analysis of TPH in (contaminated) soil. A fractional factorial design (fFD) was used to screen six factors to identify the most significant factors impacting the analysis. These factors included: injection volume (μL), injection temperature (°C), oven program (°C/min), detector temperature (°C), carrier gas flow rate (mL/min) and solvent ratio (v/v hexane/dichloromethane). The most important factors (carrier gas flow rate and oven program) were then optimized using a central composite response surface design. Robustness testing and validation of model compares favourably with the experimental results with percentage difference of 2.78% for the analysis time. This research successfully reduced the method's standard analytical time from 20 to 8min with all the carbon fractions eluting. The method was successfully applied for fast TPH analysis of Bunker C oil contaminated soil. A reduced analytical time would offer many benefits including an improved laboratory reporting times, and overall improved clean up

  3. Development, optimization, validation and application of faster gas chromatography - flame ionization detector method for the analysis of total petroleum hydrocarbons in contaminated soils.

    PubMed

    Zubair, Abdulrazaq; Pappoe, Michael; James, Lesley A; Hawboldt, Kelly

    2015-12-18

    This paper presents an important new approach to improving the timeliness of Total Petroleum Hydrocarbon (TPH) analysis in the soil by Gas Chromatography - Flame Ionization Detector (GC-FID) using the CCME Canada-Wide Standard reference method. The Canada-Wide Standard (CWS) method is used for the analysis of petroleum hydrocarbon compounds across Canada. However, inter-laboratory application of this method for the analysis of TPH in the soil has often shown considerable variability in the results. This could be due, in part, to the different gas chromatography (GC) conditions, other steps involved in the method, as well as the soil properties. In addition, there are differences in the interpretation of the GC results, which impacts the determination of the effectiveness of remediation at hydrocarbon-contaminated sites. In this work, multivariate experimental design approach was used to develop and validate the analytical method for a faster quantitative analysis of TPH in (contaminated) soil. A fractional factorial design (fFD) was used to screen six factors to identify the most significant factors impacting the analysis. These factors included: injection volume (μL), injection temperature (°C), oven program (°C/min), detector temperature (°C), carrier gas flow rate (mL/min) and solvent ratio (v/v hexane/dichloromethane). The most important factors (carrier gas flow rate and oven program) were then optimized using a central composite response surface design. Robustness testing and validation of model compares favourably with the experimental results with percentage difference of 2.78% for the analysis time. This research successfully reduced the method's standard analytical time from 20 to 8min with all the carbon fractions eluting. The method was successfully applied for fast TPH analysis of Bunker C oil contaminated soil. A reduced analytical time would offer many benefits including an improved laboratory reporting times, and overall improved clean up

  4. Gravimetric antigen detection utilizing antibody-modified lipid bilayers.

    PubMed

    Larsson, Charlotte; Bramfeldt, Hanna; Wingren, Christer; Borrebaeck, Carl; Höök, Fredrik

    2005-10-01

    Lipid bilayers containing 5% nitrilotriacetic acid (NTA) lipids supported on SiO2 have been used as a template for immobilization of oligohistidine-tagged single-chained antibody fragments (scFvs) directed against cholera toxin. It was demonstrated that histidine-tagged scFvs could be equally efficiently coupled to an NTA-Ni2+-containing lipid bilayer from a purified sample as from an expression supernatant, thereby providing a coupling method that eliminates time-consuming protein prepurification steps. Irrespective of whether the coupling was made from the unpurified or purified antibody preparation, the template proved to be efficient for antigen (cholera toxin) detection, verified using quartz crystal microbalance with dissipation monitoring. In addition, via a secondary amplification step using lipid vesicles containing GM1 (the natural membrane receptor for cholera toxin), the detection limit of cholera toxin was less than 750 pM. To further strengthen the coupling of scFvs to the lipid bilayer, scFvs containing two histidine tags, instead of just one tag, were also evaluated. The increased coupling strength provided via the bivalent anchoring significantly reduced scFv displacement in complex solutions containing large amounts of histidine-containing proteins, verified via cholera toxin detection in serum.

  5. Integrated analysis of seismological, gravimetric and structural data for identification of active faults geometries in Abruzzo and Molise areas (Italy)

    NASA Astrophysics Data System (ADS)

    Gaudiosi, Germana; Nappi, Rosa; Alessio, Giuliana; Porfido, Sabina; Cella, Federico; Fedi, Maurizio; Florio, Giovanni

    2015-04-01

    detected. The main results of our integrated analysis show a strong correlation among faults, hypocentral location of earthquakes and MDA lineaments from gravity data. Furthermore 2D seismic hypocentral locations together with high-resolution analysis of gravity anomalies have been correlated to estimate the fault systems parameters (strike, dip direction and dip angle) of some structures of the areas, through the application of the DEXP method (Fedi M. and M. Pilkington, 2012). References Fedi M., Cella F., Florio G., Rapolla A.; 2005: Multiscale Derivative Analysis of the gravity and magnetic fields of the Southern Apennines (Italy). In: Finetti I.R. (ed), CROP PROJECT: Deep Seismic Exploration of the Central Mediterranean and Italy, pp. 281-318. Fedi M., Pilkington M.; 2012: Understanding imaging methods for potential field data. Geophysics, 77: G13-G24. Gaudiosi G., Alessio G., Cella F., Fedi M., Florio G., Nappi, R.; 2012: Multiparametric data analysis for seismic sources identification in the Campanian area: merging of seismological, structural and gravimetric data. BGTA,. Vol. 53, n. 3, pp. 283-298.

  6. [Proteins from hydrocarbon fermentation].

    PubMed

    Champagnat, A

    1975-06-01

    The research work for the culture of yeasts on hydrocarbon substrates has started in 1959 at the research laboratory of Lavera in France, under Champagnat as leader. Its result is the construction and exploitation of 2 industrial plants in France and England, and a new big one is being built in Italy. The paper describes the various hydrocarbon substrates in use or proposed, and the two BP processes. It gives the main characteristics of the yeasts produced. It emphasizes the methods used for the evaluation of the yeasts both toxicologically and nutritionally by independent organizations of international level. A number of tables are given upon the nutritional performances of the yeasts on farm animals. Authorizations of use have been obtained from the hygiene authorities of the main European countries. The use for human consumption is now being considered.

  7. Tunable Gravimetric and Volumetric Hydrogen Storage Capacities in Polyhedral Oligomeric Silsesquioxane Frameworks.

    PubMed

    Deshmukh, Amol; Chiu, Cheng-Chau; Chen, Yun-Wen; Kuo, Jer-Lai

    2016-09-28

    We study the hydrogen adsorption in porous frameworks composed of silsesquioxane cages linked via boron substituted aromatic structures by first-principles modeling. Such polyhedral oligomeric silsesquioxane (POSS) frameworks can be further modified by decorating them with metal atoms binding to the ring structures of the linkers. We have considered Sc- and Ti-doped frameworks which bind H2 via so-called Kubas interaction between hydrogen molecules and transition metal atoms. It will be demonstrated that the maximum H2 gravimetric capacity can be improved to more than 7.5 wt % by using longer linkers with more ring structures. However, the maximum H2 volumetric capacity can be tuned to more than 70 g/L by varying the size of silsesquioxane cages. We are optimistic that by varying the building blocks, POSS frameworks can be modified to meet the targets for the gravimetric and volumetric capacities set by the U.S. Department of Energy.

  8. Tunable Gravimetric and Volumetric Hydrogen Storage Capacities in Polyhedral Oligomeric Silsesquioxane Frameworks.

    PubMed

    Deshmukh, Amol; Chiu, Cheng-Chau; Chen, Yun-Wen; Kuo, Jer-Lai

    2016-09-28

    We study the hydrogen adsorption in porous frameworks composed of silsesquioxane cages linked via boron substituted aromatic structures by first-principles modeling. Such polyhedral oligomeric silsesquioxane (POSS) frameworks can be further modified by decorating them with metal atoms binding to the ring structures of the linkers. We have considered Sc- and Ti-doped frameworks which bind H2 via so-called Kubas interaction between hydrogen molecules and transition metal atoms. It will be demonstrated that the maximum H2 gravimetric capacity can be improved to more than 7.5 wt % by using longer linkers with more ring structures. However, the maximum H2 volumetric capacity can be tuned to more than 70 g/L by varying the size of silsesquioxane cages. We are optimistic that by varying the building blocks, POSS frameworks can be modified to meet the targets for the gravimetric and volumetric capacities set by the U.S. Department of Energy. PMID:27599537

  9. Morphometric analysis of oleic acid-induced permeability pulmonary edema: correlation with gravimetric lung water.

    PubMed

    Darien, B J; Saban, M R; Hart, A P; MacWilliams, P S; Clayton, M K; Kruse-Elliott, K T

    1997-07-01

    The technique used most commonly to quantitate pulmonary edema in in vivo animal models is postmortem gravimetric analysis (wet:dry) ratio. To determine whether lung water can be quantitated morphometrically, as accurately as by the commonly used gravimetric analysis, perivascular edema (cuff) area to vessel area ratio was correlated to wet:dry ratio. Anesthetized pigs were given either oleic acid (20 mg/kg/h, intravenously) or physiologic saline. At 4 h, lungs were excised and cuff:vessel and wet:dry ratio analysis was performed. The intermediate lobe was clamped across its main stem bronchus to maintain peak inspiratory inflation, excised, frozen in liquid nitrogen, and stored at -70 degrees C until cryostat sectioning and quantification of perivascular interstitial edema (cuff) area. Gravimetric analysis (wet:dry ratio) was performed on the remaining lung. Mean cuff:vessel and wet:dry analyzes showed that lung water increased significantly (p < .01) in the oleic-acid treated group (4.9 +/- .22 and 6.78 +/- .47, respectively), compared with the saline group (.03 +/- .02 and 2.55 +/- .27, respectively). The correlation coefficient between mean cuff:vessel and wet:dry ratios was .86 (p = .0016). This study demonstrates that cuff:vessel ratio analysis can be used to identify the distribution of edema fluid versus vessel diameter, and seems to be as effective a technique as gravimetric analysis to quantitate lung water changes in acute lung injury models. Moreover cuff:vessel ratio analysis can differentiate modest changes in pulmonary edema by direct quantitation, an important end-point not provided by wet:dry analysis. Therefore, it may be a more sensitive technique when investigating therapeutic interventions in in vivo models of acute lung injury.

  10. Preliminary estimates of Gulf Stream characteristics from TOPEX data and a precise gravimetric geoid

    NASA Technical Reports Server (NTRS)

    Rapp, Richard H.; Smith, Dru A.

    1994-01-01

    TOPEX sea surface height data has been used, with a gravimetric geoid, to calculate sea surface topography across the Gulf Stream. This topography was initially computed for nine tracks on cycles 21 to 29. Due to inaccurate geoid undulations on one track, results for eight tracks are reported. The sea surface topography estimates were used to calculate parameters that describe Gulf Stream characteristics from two models of the Gulf Stream. One model was based on a Gaussian representation of the velocity while the other was a hyperbolic representation of velocity or the sea surface topography. The parameters of the Gaussian velocity model fit were a width parameter, a maximum velocity value, and the location of the maximum velocity. The parameters of the hyperbolic sea surface topography model were the width, the height jump, position, and sea surface topography at the center of the stream. Both models were used for the eight tracks and nine cycles studied. Comparisons were made between the width parameters, the maximum velocities, and the height jumps. Some of the parameter estimates were found to be highly (0.9) correlated when the hyperbolic sea surface topography fit was carried out, but such correlations were reduced for either the Gaussian velocity fits or the hyperbolic velocity model fit. A comparison of the parameters derived from 1-year TOPEX data showed good agreement with values derived by Kelly (1991) using 2.5 years of Geosat data near 38 deg N, 66 deg W longitude. Accuracy of the geoid undulations used in the calculations was of order of +/- 16 cm with the accuracy of a geoid undulation difference equal to +/- 15 cm over a 100-km line in areas with good terrestrial data coverage. This paper demonstrates that our knowledge or geoid undulations and undulation differences, in a portion of the Gulf Stream region, is sufficiently accurate to determine characteristics of the jet when used with TOPEX altimeter data. The method used here has not been shown to

  11. A precise gravimetric geoid model for the Gulf of Corinth (KTH-COR12)

    NASA Astrophysics Data System (ADS)

    Daras, I.; Papazissi, K.; Pail, R.; Marinou, A.; Fairhead, D.

    2012-04-01

    Greece is a very active region where three major tectonic plates, the Eurasia, Africa, and Arabia plates meet. The motions of those major plates drive smaller plates, like the Aegean Sea plate, whose shape and motion determine the locations and focal mechanisms of most earthquakes in the region. The northern edge of the Aegean Sea plate is the Eurasian plate which is a divergent boundary responsible for the formation of the Gulf of Corinth. As a result our area of interest is the most rapidly extending rift system in Greece connected with the highest seismic activities in the Euro-Mediterranean region, an estimate of 1 to 1.5 cm/year of north-south extension, frequent seismic swarms, and destructive historical earthquakes. The key to a better monitoring of the regional earth crustal movements is the use of accurate orthometric heights stemming from GPS geometric heights and a precise geoid model. A precise gravimetric geoid model of the Gulf of Corinth has been computed using the least squares modification of Stokes formula developed at KTH (KTH method). In this method, a stochastic approach applies additional information about the potential coefficients and the gravity anomaly errors in combination with the least squares modification of Stokes kernel to minimize the expected global mean square error (MSE). For this purpose, a dataset of local terrestrial gravity anomalies was combined with a global geopotential model, namely the ITG-Grace2010s satellite-only gravity field model. Areas with no terrestrial gravity information (i.e. sea regions) were filled with EGM08 gravity anomaly values. The SRTM90 digital elevation data from Shuttle Radar Topographic Mission (SRTM) of NASA, with a 90m resolution was chosen for the, essential for the computations, DEM. Additionally, GPS/Levelling, mean sea surface (MSS) and mean dynamic topography (MDT) datasets were used for externally evaluating the geoid model. In this poster the methodology behind the construction of the KTH

  12. THERMOCHEMISTRY OF HYDROCARBON RADICALS

    SciTech Connect

    Kent M. Ervin, Principal Investigator

    2004-08-17

    Gas phase negative ion chemistry methods are employed to determine enthalpies of formation of hydrocarbon radicals that are important in combustion processes and to investigate the dynamics of ion-molecule reactions. Using guided ion beam tandem mass spectrometry, we measure collisional threshold energies of endoergic proton transfer and hydrogen atom transfer reactions of hydrocarbon molecules with negative reagent ions. The measured reaction threshold energies for proton transfer yield the relative gas phase acidities. In an alternative methodology, competitive collision-induced dissociation of proton-bound ion-molecule complexes provides accurate gas phase acidities relative to a reference acid. Combined with the electron affinity of the R {center_dot} radical, the gas phase acidity yields the RH bond dissociation energy of the corresponding neutral molecule, or equivalently the enthalpy of formation of the R{center_dot} organic radical, using equation: D(R-H) = {Delta}{sub acid}H(RH) + EA(R) - IE(H). The threshold energy for hydrogen abstraction from a hydrocarbon molecule yields its hydrogen atom affinity relative to the reagent anion, providing the RH bond dissociation energy directly. Electronic structure calculations are used to evaluate the possibility of potential energy barriers or dynamical constrictions along the reaction path, and as input for RRKM and phase space theory calculations. In newer experiments, we have measured the product velocity distributions to obtain additional information on the energetics and dynamics of the reactions.

  13. H-H, C-H, and C-C NMR spin-spin coupling constants calculated by the FP-INDO method for aromatic hydrocarbons

    NASA Technical Reports Server (NTRS)

    Long, S. A. T.; Memory, J. D.

    1978-01-01

    The FP-INDO (finite perturbation-intermediate neglect of differential overlap) method is used to calculate the H-H, C-H, and C-C coupling constants in hertz for molecules of six different benzenoid hydrocarbons: benzene, naphthalene, biphenyl, anthracene, phenanthrene, and pyrene. The calculations are based on both the actual and the average molecular geometries. It is found that only the actual molecular geometries can always yield the correct relative order of values for the H-H coupling constants. For the calculated C-C coupling constants, as for the calculated C-H coupling constants, the signs are positive (negative) for an odd (even) number of bonds connecting the two nuclei. Agreements between the calculated and experimental values of the coupling constants for all six molecules are comparable to those reported previously for other molecules.

  14. Carbonaceous species methods comparison study at Citrus College. Task: analysis for trace hydrocarbons and related halocarbons in urban ambient air samples. Final report

    SciTech Connect

    Rasmussen, R.A.

    1987-10-01

    As part of the ARB-sponsored Carbonaceous Species Methods Comparison Study (CSMCS) in Glendora, CA, from August 11-21, 1986, time-integrated, ambient samples were collected in stainless steel canisters. Five samples per day were collected, ranging from 4 to 8 hours according to the CSMCS protocol. The species measured included CO, CH/sub 4/, CO/sub 2/, H/sub 2/, and the C/sub 2/ through C10 hydrocarbons. In addition, N/sub 2/O, the halocarbons F-12, F-11, F-113, CHCl/sub 3/, CH/sub 3/CCl/sub 3/, CCl/sub 4/, C/sub 2/HCl/sub 3/ and C/sub 2/Cl/sub 4/ were measured. Four gas-chromatograph systems were used to quantify these species. The report contains tables of concentrations of the species measured at the South Coast Air Basin site during smoggy summer conditions.

  15. Model studies for evaluating the acute neurobehavioral effects of complex hydrocarbon solvents I. Validation of methods with ethanol.

    PubMed

    McKee, R H; Lammers, J H C M; Hoogendijk, E M G; Emmen, H H; Muijser, H; Barsotti, D A; Owen, D E; Kulig, B M

    2006-12-01

    As a preliminary step to evaluating the acute neurobehavioral effects of hydrocarbon solvents and to establish a working model for extrapolating animal test data to humans, joint neurobehavioral/toxicokinetic studies were conducted which involved administering ethanol to rats and volunteers. The specific objectives of the present studies were to evaluate the acute central nervous system (CNS) effects of ethanol in rats and humans and to assess relationships between internal levels of exposure and behavioral effects. A more general objective was to validate a battery of neurobehavioral tests that could be used to carry out comparative studies in both species. Accordingly, a range of tests including standardized observational measures, spontaneous motor activity assessments and learned visual discrimination performance was utilized in rat studies to evaluate acute CNS effects. Groups of rats were given ethanol at levels of approximately 0.5, 1.0 or 2.0g/kg, with blood level measurements to verify internal doses. In a volunteer study, 12 healthy male subjects were given 0.65g/kg ethanol, a level approximating the limit for motor vehicle operation in The Netherlands, and neurobehavioral effects were measured prior to and 1 and 3h after ethanol administration, with a computerized neurobehavioral test battery. Blood and air measurements were made to quantify internal doses. Results of the behavioral tests in rats provided evidence of ethanol-induced changes in neuromuscular, sensori-motor, and activity domains. There were also significant changes in visual discrimination, particularly in the areas of general measures of responding and psychomotor speed. In humans there were small but statistically significant effects on learning and memory, psychomotor skills and attention. However, the effects were subtle and not all parameters within given domains were affected. These studies demonstrated a qualitative similarity in response between rats and humans.

  16. Report of EPA efforts to replace freon for the determination of oil and grease and total petroleum hydrocarbons: Phase 2

    SciTech Connect

    1995-04-01

    The Environmental Protection Agency (EPA) initiated a multiphase study to determine a suitable replacement solvent for Freon-113, a class I CFC used in several EPA wastewater and solid waste methods for the determination of oil and grease and petroleum hydrocarbons. Conclusions from the Phase I study were used to narrow the list of alternative solvents to be considered in Phase II to n-hexane and cyclohexane. These solvents were evaluated for separatory funnel extraction and gravimetric determination of both oil and grease and total petroleum hydrocarbons (TPH) in aqueous samples. Triplicate analyses were performed for each of the solvents tested (i.e Freon-113, n-hexane, and cyclohexane) on each of 34 samples from a combination of inprocess and effluent waste streams collected from 25 facilities encompassing 16 different industrial categories. The objectives of Phase II were to find the alternative solvent that produced results closest to the results produced by Freon-113 and to develop an analytical method that incorporated this extraction solvent. In addition to studies of alternative solvents, solid phase disk extraction, solid phase cartridge extraction (also known as solid phase column extraction), non-dispersive infra-red spectroscopy, and immunoassay were voluntarily evaluated by vendors of the products using splits of each sample collected as part of the Phase II study.

  17. Formulation and analysis of food-grade mineral hydrocarbons in toxicology studies.

    PubMed

    Walters, D G; Sherrington, K V; Worrell, N; Riley, R A

    1994-06-01

    Methods are presented for the formulation and rapid determination of mineral hydrocarbons (MHCs) in animal diet and tissue. Food grade white oils and low melting point waxes are mixed as liquids with powdered diet. Higher melting point waxes are first powdered using a novel atomization technique before dry mixing with diet. MHCs sufficiently soluble in carbon tetrachloride (CCl4) are determined in diet by ultrasonic solvent extraction, adsorption of polar material on Florisil and analysis of the residue by quantitative Fourier Transform Infra Red (FT-IR) spectroscopy. Quantification in tissue is achieved by aqueous saponification, followed by extraction, clean-up and FT-IR analysis as for diet samples. A 10-fold increase in sensitivity over previous methods is achieved, below 0.002% (w/w) in diet and 0.1 mg/g in tissue. Over 80% of the CCl4 used can be recovered and recycled. Control diet seems to contain approximately 0.003% (w/w) background MHC. The method was modified for one powdered wax, only sparingly soluble in CCl4, high concentrations being extracted from diet by flotation in aqueous cetrimide and determined gravimetrically with a limit of detection of 0.1% (w/w) in diet. Application of these methods to 90-day feeding studies is described, and future developments due to the phasing out of CCl4 are discussed.

  18. Steam Hydrocarbon Cracking and Reforming

    ERIC Educational Resources Information Center

    Golombok, Michael

    2004-01-01

    The interactive methods of steam hydrocarbon reforming and cracking of the oil and chemical industries are scrutinized, with special focus on their resemblance and variations. The two methods are illustrations of equilibrium-controlled and kinetically-controlled processes, the analysis of which involves theories, which overlap and balance each…

  19. Production of hydrocarbons from hydrates. [DOE patent application

    DOEpatents

    McGuire, P.L.

    1981-09-08

    An economical and safe method of producing hydrocarbons (or natural gas) from in situ hydrocarbon-containing hydrates is given. Once started, the method will be self-driven and will continue producing hydrocarbons over an extended period of time (i.e., many days).

  20. Hydrocarbon conversion process

    SciTech Connect

    Ting, P.B.; Simpson, H.D.

    1986-02-04

    This patent describes a catalytic refining process in which a hydrocarbon oil is upgraded by contact with a particulate catalyst under conditions of elevated temperature and pressure in the presence of hydrogen. The catalyst, is made of a composition prepared by the method consisting of: (1) impregnating support particles with an aqueous impregnating solution comprising one or more dissolved Group VIB metal components and citric acid, in which the solution has a pH less than 1.0; and (2) calcining the impregnated support particles.

  1. Efficacy of head space solid-phase microextraction coupled to gas chromatography-mass spectrometry method for determination of the trace extracellular hydrocarbons of cyanobacteria.

    PubMed

    Guan, Wenna; Zhu, Tao; Wang, Yuejie; Zhang, Zhongyi; Jin, Zhao; Wang, Cong; Bai, Fali

    2016-09-01

    Hydrocarbons are widespread in cyanobacteria, and the biochemical synthetic pathways were recently identified. Intracellular fatty alka(e)nes of cyanobacteria have been detected by liquid-liquid extraction (LLE) coupled to gas chromatography-mass spectrometry (GC/MS). However, whether fatty alka(e)nes can be released to cyanobacterial culture media remains to be clarified. This work develops a sensitive method for analyzing the trace level of extracellular hydrocarbons in cyanobacterial culture media by head space solid-phase microextraction (HS-SPME) coupled to GC/MS. Headspace (HS) extraction mode using polydimethylsiloxane fiber to extract for 30min at 50°C was employed as the optimal extraction conditions. Five cyanobacterial fatty alka(e)nes analogs including pentadecene (C15:1), pentadecane (C15:0), heptadecene (C17:1), heptadecane (C17:0), nonadecane (C19:0) were analyzed, and the data obtained from HS-SPME-GC/MS method were quantified using internal standard peak area comparisons. Limits of detection (LOD), limits of quantitation (LOQ), linear dynamic range, precisions (RSD) and recovery for the analysis of extracellular fatty alka(e)nes of cyanobacteria by HS-SPME-GC/MS were evaluated. The LODs limits of detection (S/N = 3) varied from 10 to 21 ng L-1. The correlation coefficients (r) of the calibration curves ranged from 0.9873 to 0.9977 with a linearity from 0.1 to 50 μg L-1. The RSD values were ranging from 7.8 to 14.0% and from 4.0 to 8.8% at 1.0 μg L-1 and 10.0 μg L-1 standard solutions, respectively. Comparative analysis of extracellular fatty alka(e)nes in the culture media of model cyanobacteria Synechocystis sp. PCC 6803 demonstrated that sensitivity of HS-SPME-GC/MS method was significantly higher than LLE method. Finally, we found that heptadecane can be released into the culture media of Synechocystis sp. PCC 6803 at the later growth period. PMID:27428454

  2. Efficacy of head space solid-phase microextraction coupled to gas chromatography-mass spectrometry method for determination of the trace extracellular hydrocarbons of cyanobacteria.

    PubMed

    Guan, Wenna; Zhu, Tao; Wang, Yuejie; Zhang, Zhongyi; Jin, Zhao; Wang, Cong; Bai, Fali

    2016-09-01

    Hydrocarbons are widespread in cyanobacteria, and the biochemical synthetic pathways were recently identified. Intracellular fatty alka(e)nes of cyanobacteria have been detected by liquid-liquid extraction (LLE) coupled to gas chromatography-mass spectrometry (GC/MS). However, whether fatty alka(e)nes can be released to cyanobacterial culture media remains to be clarified. This work develops a sensitive method for analyzing the trace level of extracellular hydrocarbons in cyanobacterial culture media by head space solid-phase microextraction (HS-SPME) coupled to GC/MS. Headspace (HS) extraction mode using polydimethylsiloxane fiber to extract for 30min at 50°C was employed as the optimal extraction conditions. Five cyanobacterial fatty alka(e)nes analogs including pentadecene (C15:1), pentadecane (C15:0), heptadecene (C17:1), heptadecane (C17:0), nonadecane (C19:0) were analyzed, and the data obtained from HS-SPME-GC/MS method were quantified using internal standard peak area comparisons. Limits of detection (LOD), limits of quantitation (LOQ), linear dynamic range, precisions (RSD) and recovery for the analysis of extracellular fatty alka(e)nes of cyanobacteria by HS-SPME-GC/MS were evaluated. The LODs limits of detection (S/N = 3) varied from 10 to 21 ng L-1. The correlation coefficients (r) of the calibration curves ranged from 0.9873 to 0.9977 with a linearity from 0.1 to 50 μg L-1. The RSD values were ranging from 7.8 to 14.0% and from 4.0 to 8.8% at 1.0 μg L-1 and 10.0 μg L-1 standard solutions, respectively. Comparative analysis of extracellular fatty alka(e)nes in the culture media of model cyanobacteria Synechocystis sp. PCC 6803 demonstrated that sensitivity of HS-SPME-GC/MS method was significantly higher than LLE method. Finally, we found that heptadecane can be released into the culture media of Synechocystis sp. PCC 6803 at the later growth period.

  3. Determination of polycyclic aromatic hydrocarbons from ambient air particulate matter using a cold fiber solid phase microextraction gas chromatography-mass spectrometry method.

    PubMed

    Menezes, Helvécio Costa; de Lourdes Cardeal, Zenilda

    2011-05-27

    Polycyclic aromatic hydrocarbons (PAH) from ambient air particulate matter (PM) were analyzed by a new method that utilized direct immersion (DI) and cold fiber (CF) SPME-GC/MS. Experimental design was used to optimize the conditions of extraction by DI-CF-SPME with a 100μm polydimethylsiloxane (PDMS) fiber. The optimal conditions included a 5min equilibration at 70°C time in an ultrasonic bath with an extraction time of 60min. The optimized method was validated by the analysis of a NIST standard reference material (SRM), 1649b urban dust. The results obtained were in good agreement with certified values. PAH recoveries for reference materials were between 88 and 98%, with a relative standard deviation ranging from 5 to 17%. Detection limits (LOD) varied from 0.02 to 1.16ng and the quantification limits (LOQ) varied from 0.05 to 3.86ng. The optimized and validated method was applied to the determination of PAH from real particulate matter (PM10) and total suspended particulate (TPS) samples collected on quartz fiber filters with high volume samplers.

  4. Gas chromatography-mass spectrometry (GC-MS) method for the determination of 16 European priority polycyclic aromatic hydrocarbons in smoked meat products and edible oils.

    PubMed

    Jira, W; Ziegenhals, K; Speer, K

    2008-06-01

    A gas chromatography-mass spectrometry (GC-MS) method was developed for the analysis of 15 polycyclic aromatic hydrocarbons (PAHs) highlighted as carcinogenic by the Scientific Committee on Food (SCF) plus benzo[c]fluorine (recommended to be analysed by the Joint FAO/WHO Expert Committee on Food Additives (JECFA) in fat-containing foods such as edible oils and smoked meat products. This method includes accelerated solvent extraction (ASE) and the highly automated clean-up steps gel permeation chromatography (GPC) and solid-phase extraction (SPE). Using a VF-17ms GC column, a good separation of benzo[b]fluoranthene, benzo[j]fluoranthene and benzo[k]fluoranthene was achieved. Futhermore, the six methylchrysene isomers and the PAH compounds with a molecular weight of 302 Daltons in fat-containing foods attained a better chromatographic separation in comparison with a 5-ms column. The reliability of the analytical method for edible oils was demonstrated by the results from a proficiency test. Measurements with GC-high-resolution mass spectroscopy (HRMS) and gas chromatography-mass selective detection (GC-MSD) led to comparable results. A survey of the 16 PAHs in 22 smoked meat products showed concentrations in the range < 0.01-19 microg kg(-1). The median concentration for benzo[a]pyrene was below 0.15 microg kg(-1).

  5. Single-laboratory validation of a saponification method for the determination of four polycyclic aromatic hydrocarbons in edible oils by HPLC-fluorescence detection.

    PubMed

    Akdoğan, Abdullah; Buttinger, Gerhard; Wenzl, Thomas

    2016-01-01

    An analytical method is reported for the determination of four polycyclic aromatic hydrocarbons (benzo[a]pyrene (BaP), benz[a]anthracene (BaA), benzo[b]fluoranthene (BbF) and chrysene (CHR)) in edible oils (sesame, maize, sunflower and olive oil) by high-performance liquid chromatography. Sample preparation is based on three steps including saponification, liquid-liquid partitioning and, finally, clean-up by solid phase extraction on 2 g of silica. Guidance on single-laboratory validation of the proposed analysis method was taken from the second edition of the Eurachem guide on method validation. The lower level of the working range of the method was determined by the limits of quantification of the individual analytes, and the upper level was equal to 5.0 µg kg(-1). The limits of detection and quantification of the four PAHs ranged from 0.06 to 0.12 µg kg(-1) and from 0.13 to 0.24 µg kg(-1). Recoveries of more than 84.8% were achieved for all four PAHs at two concentration levels (2.5 and 5.0 µg kg(-1)), and expanded relative measurement uncertainties were below 20%. The performance of the validated method was in all aspects compliant with provisions set in European Union legislation for the performance of analytical methods employed in the official control of food. The applicability of the method to routine samples was evaluated based on a limited number of commercial edible oil samples.

  6. Single-laboratory validation of a saponification method for the determination of four polycyclic aromatic hydrocarbons in edible oils by HPLC-fluorescence detection.

    PubMed

    Akdoğan, Abdullah; Buttinger, Gerhard; Wenzl, Thomas

    2016-01-01

    An analytical method is reported for the determination of four polycyclic aromatic hydrocarbons (benzo[a]pyrene (BaP), benz[a]anthracene (BaA), benzo[b]fluoranthene (BbF) and chrysene (CHR)) in edible oils (sesame, maize, sunflower and olive oil) by high-performance liquid chromatography. Sample preparation is based on three steps including saponification, liquid-liquid partitioning and, finally, clean-up by solid phase extraction on 2 g of silica. Guidance on single-laboratory validation of the proposed analysis method was taken from the second edition of the Eurachem guide on method validation. The lower level of the working range of the method was determined by the limits of quantification of the individual analytes, and the upper level was equal to 5.0 µg kg(-1). The limits of detection and quantification of the four PAHs ranged from 0.06 to 0.12 µg kg(-1) and from 0.13 to 0.24 µg kg(-1). Recoveries of more than 84.8% were achieved for all four PAHs at two concentration levels (2.5 and 5.0 µg kg(-1)), and expanded relative measurement uncertainties were below 20%. The performance of the validated method was in all aspects compliant with provisions set in European Union legislation for the performance of analytical methods employed in the official control of food. The applicability of the method to routine samples was evaluated based on a limited number of commercial edible oil samples. PMID:26634339

  7. Thermo Gravimetric and Differential Thermal Analysis of Clay of Western Rajasthan (india)

    NASA Astrophysics Data System (ADS)

    Shekhawat, M. S.

    The paper presents the study of thermo gravimetric and differential thermal analysis of blended clay. Western part of Rajasthan (India) is rich resource of Ball clays and it is mainly used by porcelain, sanitary ware, and tile industry. The quality and grade of clay available in the region vary from one deposit to other. To upgrade the fired colour and strength properties, different variety of clays may be blended together. The paper compares the results of thermal analysis one of blended clay B2 with reference clay of Ukraine which is imported by industries owners. The result revealed that the blended clay is having mineral kaolinite while the Ukrainian clay is Halloysite.

  8. A comparison of satellite Doppler and gravimetric geoid undulations considering terrain-corrected gravity data

    NASA Technical Reports Server (NTRS)

    Rapp, R. H.; Wichiencharoen, C.

    1984-01-01

    Geoid undulations derived from Doppler satellite positioning are compared with corresponding values derived from terrestrial and satellite information using three different procedures. Doppler undulations are compared with uncorrected gravimetric undulations, and systematic differences of 1.6 m and 0.4 m are found for western and eastern U.S. stations, respectively. The systematic difference of 1.6 m was reduced to 0.1 m when terrain-related corrections were applied. Undulations computed from a spherical harmonic expansion to degree 180 yielded standard deviations only slightly poorer than the combined data. A more systematic difference in the western than in the eastern stations remained.

  9. Conversion of organic solids to hydrocarbons

    DOEpatents

    Greenbaum, Elias

    1995-01-01

    A method of converting organic solids to liquid and gaseous hydrocarbons includes impregnating an organic solid with photosensitizing ions and exposing the impregnated solid to light in a non-oxidizing atmosphere for a time sufficient to photocatalytically reduce the solid to at least one of a liquid and a gaseous hydrocarbon.

  10. Conversion of organic solids to hydrocarbons

    DOEpatents

    Greenbaum, E.

    1995-05-23

    A method of converting organic solids to liquid and gaseous hydrocarbons includes impregnating an organic solid with photosensitizing ions and exposing the impregnated solid to light in a non-oxidizing atmosphere for a time sufficient to photocatalytically reduce the solid to at least one of a liquid and a gaseous hydrocarbon. 5 Figs.

  11. Part A: Hydrocarbon Suspension in Slush Hydrogen

    NASA Technical Reports Server (NTRS)

    Sindt, C. F.

    1972-01-01

    Methods of preparing suspensions of a hydrocarbon in slush hydrogen for nuclear fuel element corrosion inhibition in rocket engines were investigated. Suspensions were prepared using approximately 5000 ppm by mass of methane, ethane, or cyclopropane in slush hydrogen. The suspensions were stable in the slush, but the hydrocarbons settled out of the liquid melt.

  12. Characterization of a pressurized C5-C16 hydrocarbon gas calibration standard for air analysis.

    PubMed

    Helmig, Detlev; Revermann, Tobias; Hall, Bradley

    2004-11-15

    A compressed gas standard containing parts-per-billion (ppb) amounts of the volatile hydrocarbons methylpentadiene (isoprene, 540 ppb) and isooctane (259 ppb) and a series of less volatile C12-C16 n-alkanes (n-dodecane, 349 ppb; n-tridecane, 340 ppb; n-tetradecane, 202 ppb; n-pentadecane, 271 ppb; and n-hexadecane, 308 ppb) was prepared by a one-step (no further gas dilution) microgravimetric method. The gravimetric mixing ratios were confirmed by referencing to a capillary diffusion method. The cylinder was heated to 75 degrees C to minimize condensation losses of analytes to the cylinder walls. Mixing ratios were monitored over a 2.5-year period. Some initial analyte losses (approximately 3 to 20%) were observed for the heavier C14-C16 n-alkanes. Subsequently, analyte loss rates were found to be in the range of <1.0% per year for n-dodecane to n-hexadecane. The developed guidelines for preparation, storage, and retrieval of these semivolatile analytes enable the use of compressed gas standards for calibration and method development purposes in the environmental gas-phase analysis of these and related compounds.

  13. Evaluation of Polycyclic Aromatic Hydrocarbons Using Analytical Methods, Toxicology, and Risk Assessment Research: Seafood Safety after a Petroleum Spill as an Example

    PubMed Central

    Overton, Edward; Frickel, Scott; Howard, Jessi; Wilson, Mark; Simon, Bridget; Echsner, Stephen; Nguyen, Daniel; Gauthe, David; Blake, Diane; Miller, Charles; Elferink, Cornelis; Ansari, Shakeel; Fernando, Harshica; Trapido, Edward; Kane, Andrew

    2013-01-01

    Background: Polycyclic aromatic hydrocarbons (PAHs) are abundant and widespread environmental chemicals. They are produced naturally and through man-made processes, and they are common in organic media, including petroleum. Several PAHs are toxic, and a subset exhibit carcinogenic activity. PAHs represent a range of chemical structures based on two or more benzene rings and, depending on their source, can exhibit a variety of side modifications resulting from oxygenation, nitrogenation, and alkylation. Objectives: Here we discuss the increasing ability of contemporary analytical methods to distinguish not only different chemical structures among PAHs but also their concentrations in environmental media. Using seafood contamination following the Deepwater Horizon accident as an example, we identify issues that are emerging in the PAH risk assessment process because of increasing analytical sensitivity for individual PAHs, and we describe the paucity of toxicological literature for many of these compounds. Discussion: PAHs, including the large variety of chemically modified or substituted PAHs, are naturally occurring and may constitute health risks if human populations are exposed to hazardous levels. However, toxicity evaluations have not kept pace with modern analytic methods and their increased ability to detect substituted PAHs. Therefore, although it is possible to measure these compounds in seafood and other media, we do not have sufficient information on the potential toxicity of these compounds to incorporate them into human health risk assessments and characterizations. Conclusions: Future research efforts should strategically attempt to fill this toxicological knowledge gap so human health risk assessments of PAHs in environmental media or food can be better determined. This is especially important in the aftermath of petroleum spills. Citation: Wickliffe J, Overton E, Frickel S, Howard J, Wilson M, Simon B, Echsner S, Nguyen D, Gauthe D, Blake D, Miller C

  14. Validation of an Analytical Method for Determination of 13 priority polycyclic aromatic hydrocarbons in mineral water using dispersive liquid-liquid microextraction and GC-MS

    PubMed Central

    Sadeghi, Ramezan; Kobarfard, Farzad; Yazdanpanah, Hassan; Eslamizad, Samira; Bayat, Mitra

    2016-01-01

    Dispersive liquid-liquid microextraction (DLLME) combined with gas chromatography–mass spectrometry (GC–MS) was used for the extraction and determination of 13 polycyclic aromatic hydrocarbons (PAHs) in mineral water samples. In this procedure, the suitable combination of extraction solvent (500 µL chloroform) and disperser solvent (1000 µL acetone) were quickly injected into the water sample (10.00 mL) by Hamilton syringe. After centrifugation, 500 µL of the lower organic phase was dried under a gentle stream of nitrogen, re-dissolved in chloroform and injected into GC-MS. Chloroform and acetone were found to be the best extraction and disperser solvent, respectively. Validation of the method was performed using spiked calibration curves. The enrichment factor ranged from 93 to 129 and the recovery ranged from 71 to 90%. The linear ranges for all the PAHs were 0.10-2.80 ngmL-1. The relative standard deviations (RSDs) of PAHs in water by using anthracene-d10 as internal standard, were in the range of 4-11% for most of the analytes (n = 3). Limit of detection (LOD) for different PAHs were between 0.03 and 0.1 ngmL-1. The method was successfully applied for the analysis of PAHs in mineral water samples collected from Tehran. PMID:27610156

  15. Evaluation of sampling and analytical methods for nicotine and polynuclear aromatic hydrocarbon in indoor air. Final report, 1 February 1987-30 March 1987

    SciTech Connect

    Chuang, J.C.; Kuhlman, M.R.; Hannan, S.W.; Bridges, C.

    1987-11-01

    The objective of this project was to evaluate a potential collection medium, XAD-4 resin, for collecting nicotine and polynuclear aromatic hydrocarbon (PAH) and to determine whether one collection system and one analytical method will allow quantification of both compound classes in air. The extraction efficiency study was to determine the extraction method to quantitatively remove nicotine and PAH from XAD-4 resin. The results showed that a two-step Soxhlet extraction consisting of dichloromethane followed by ethyl acetate resulted in the best recoveries for both nicotine and PAH. In the sampling efficiency study, XAD-2 and XAD-4 resin were compared, in parallel, for collection of PAH and nicotine. Quartz fiber filters were placed upstream of both adsorbents to collect particles. Prior to sampling, both XAD-2 and XAD-4 traps were spiked with known amounts (2 microgram) of perdeuterated PAH and D3-nicotine. The experiments were performed with cigarette smoking and nonsmoking conditions. The spiked PAH were retained well in both adsorbents after exposure to more than 300 cu. m. of indoor air. The spiked XAD-4 resin gave higher recoveries for D3-nicotine than did the spiked XAD-2 resin. The collection efficiency for PAH for both adsorbents is very similar but higher levels of nicotine were collected on XAD-4 resin.

  16. Validation of an Analytical Method for Determination of 13 priority polycyclic aromatic hydrocarbons in mineral water using dispersive liquid-liquid microextraction and GC-MS.

    PubMed

    Sadeghi, Ramezan; Kobarfard, Farzad; Yazdanpanah, Hassan; Eslamizad, Samira; Bayat, Mitra

    2016-01-01

    Dispersive liquid-liquid microextraction (DLLME) combined with gas chromatography-mass spectrometry (GC-MS) was used for the extraction and determination of 13 polycyclic aromatic hydrocarbons (PAHs) in mineral water samples. In this procedure, the suitable combination of extraction solvent (500 µL chloroform) and disperser solvent (1000 µL acetone) were quickly injected into the water sample (10.00 mL) by Hamilton syringe. After centrifugation, 500 µL of the lower organic phase was dried under a gentle stream of nitrogen, re-dissolved in chloroform and injected into GC-MS. Chloroform and acetone were found to be the best extraction and disperser solvent, respectively. Validation of the method was performed using spiked calibration curves. The enrichment factor ranged from 93 to 129 and the recovery ranged from 71 to 90%. The linear ranges for all the PAHs were 0.10-2.80 ngmL(-1). The relative standard deviations (RSDs) of PAHs in water by using anthracene-d10 as internal standard, were in the range of 4-11% for most of the analytes (n = 3). Limit of detection (LOD) for different PAHs were between 0.03 and 0.1 ngmL(-1). The method was successfully applied for the analysis of PAHs in mineral water samples collected from Tehran. PMID:27610156

  17. Distribution of polycyclic aromatic hydrocarbons in southern Chesapeake Bay surface water: Evaluation of three methods for determining freely dissolved water concentrations

    SciTech Connect

    Gustafson, K.E.; Dickhut, R.M.

    1997-03-01

    Gas sparging, semipermeable-membrane devices (SPMDs), and filtration with sorption of dissolved polycyclic aromatic hydrocarbons (PAHs) to XAD-2 resin were evaluated for determining the concentrations of freely dissolved PAHs in estuarine waters of southern Chesapeake Bay at sites ranging from rural to urban and highly industrialized. Gas sparging had significant sampling artifacts due to particle scavenging by rising bubbles, and SPMDs were kinetically limited for four-ring and larger PAHs relative to short-term temporal changes in water concentrations. Filtration with sorption of the dissolved contaminant fraction to XAD-2 resin was found to be the most accurate and feasible method for determining concentrations of freely dissolved PAHs in estuarine water. Concentrations and distribution coefficients of dissolved and particulate PAHs were measured using the filtration/XAD-2 method. Concentrations of PAHs in surface waters of southern Chesapeake Bay were higher than those reported for the northern bay; concentrations in the Elizabeth River were elevated relative to all other sites. A gradient for particulate PAHs was observed from urban to remote sites. No seasonal trends were observed in dissolved or particle-bound PAH fractions at any site. Distributions of dissolved and particulate PAHs in surface waters of the Chesapeake Bay are near equilibrium at all locations and during all seasons.

  18. Validation of an Analytical Method for Determination of 13 priority polycyclic aromatic hydrocarbons in mineral water using dispersive liquid-liquid microextraction and GC-MS

    PubMed Central

    Sadeghi, Ramezan; Kobarfard, Farzad; Yazdanpanah, Hassan; Eslamizad, Samira; Bayat, Mitra

    2016-01-01

    Dispersive liquid-liquid microextraction (DLLME) combined with gas chromatography–mass spectrometry (GC–MS) was used for the extraction and determination of 13 polycyclic aromatic hydrocarbons (PAHs) in mineral water samples. In this procedure, the suitable combination of extraction solvent (500 µL chloroform) and disperser solvent (1000 µL acetone) were quickly injected into the water sample (10.00 mL) by Hamilton syringe. After centrifugation, 500 µL of the lower organic phase was dried under a gentle stream of nitrogen, re-dissolved in chloroform and injected into GC-MS. Chloroform and acetone were found to be the best extraction and disperser solvent, respectively. Validation of the method was performed using spiked calibration curves. The enrichment factor ranged from 93 to 129 and the recovery ranged from 71 to 90%. The linear ranges for all the PAHs were 0.10-2.80 ngmL-1. The relative standard deviations (RSDs) of PAHs in water by using anthracene-d10 as internal standard, were in the range of 4-11% for most of the analytes (n = 3). Limit of detection (LOD) for different PAHs were between 0.03 and 0.1 ngmL-1. The method was successfully applied for the analysis of PAHs in mineral water samples collected from Tehran.

  19. Loss of particle nitrate from teflon sampling filters: effects on measured gravimetric mass in California and in the IMPROVE network.

    PubMed

    Ashbaugh, Lowell L; Eldred, Robert A

    2004-01-01

    The extent of mass loss on Teflon filters caused by ammonium nitrate volatilization can be a substantial fraction of the measured particulate matter with an aerodynamic diameter less than 2.5 microm (PM2.5) or 10 microm (PM10) mass and depends on where and when it was collected. There is no straightforward method to correct for the mass loss using routine monitoring data. In southern California during the California Acid Deposition Monitoring Program, 30-40% of the gravimetric PM2.5 mass was lost during summer daytime. Lower mass losses occurred at more remote locations. The estimated potential mass loss in the Interagency Monitoring of Protected Visual Environments network was consistent with the measured loss observed in California. The biased mass measurement implies that use of Federal Reference Method data for fine particles may lead to control strategies that are biased toward sources of fugitive dust, other primary particle emission sources, and stable secondary particles (e.g., sulfates). This analysis clearly supports the need for speciated analysis of samples collected in a manner that preserves volatile species. Finally, although there is loss of volatile nitrate (NO3-) from Teflon filters during sampling, the NO3- remaining after collection is quite stable. We found little loss of NO3- from Teflon filters after 2 hr under vacuum and 1 min of heating by a cyclotron proton beam.

  20. Characterizing hydrocarbon sulfonates and utilization of hydrocarbon sulfonates in oil recovery

    SciTech Connect

    Glinsmann, G.R.; Hedges, J.H.

    1982-05-18

    A method for determining the average equivalent weight of hydrocarbon sulfonates and the optimal salinity and unique salinity of surfactant systems containing such hydrocarbon sulfonates is based on the discovery that the average equivalent weights of hydrocarbon sulfonates vary inversely and linearly as the optimal salinities and unique salinities of surfactant systems containing such hydrocarbon sulfonates vary. Methods of preparing surfactant systems for the displacement of oil from subterranean reservoirs and for the displacement of oil from subterranean reservoirs, based on the above-mentioned relationships, are also disclosed.

  1. Rapid and sensitive method for the determination of four EU marker polycyclic aromatic hydrocarbons in cereal-based foods using isotope-dilution GC/MS.

    PubMed

    Kacmaz, Sibel; Zelinkova, Zuzana; Wenzl, Thomas

    2016-01-01

    A rapid and sensitive method has been developed for the determination of the four European Union marker polycyclic aromatic hydrocarbons (PAHs; benz[a]anthracene, chrysene, benzo[b]fluoranthene and benzo[a]pyrene) in some cereal-based foods. The method is based on pressurised liquid extraction (PLE), solid-phase extraction clean-up (SPE) and isotope-dilution gas chromatography with mass-spectrometric detection (GC/MS). The developed method was calibrated for the content range of 0.05-12.5 µg kg(-1) (expressed on a product basis). Recoveries of PAH were monitored in each sample via the recovery of (13)C-labelled PAHs. Recovery values were in the range between 86% and 91%, with relative standard deviations (RSDs) between 5% and 9%. The achieved limits of detection for all analytes were below 0.05 µg kg(-1). The applicability of the method for the analysis of routine samples was studied by the analysis of a set of commercial bread and breakfast cereal samples. In all analysed samples, benzo[a]pyrene (BAP) was the most prevalent PAH with the content between 0.09 and 0.30 µg kg(-1). On average, samples showed low levels of the sum of the four EU marker PAHs (ΣPAH4) that ranged between 0.11 and 0.22 µg kg(-1) for bread samples and between 0.23 and 0.87 µg kg(-1) for breakfast cereal samples. The developed method was found suitable for the determination of PAHs in cereal-based foods like cornflakes and breads with total relative fat contents below 3.5%. PMID:26950570

  2. Biological enhancement of hydrocarbon extraction

    DOEpatents

    Brigmon, Robin L.; Berry, Christopher J.

    2009-01-06

    A method of microbial enhanced oil recovery for recovering oil from an oil-bearing rock formation is provided. The methodology uses a consortium of bacteria including a mixture of surfactant producing bacteria and non-surfactant enzyme producing bacteria which may release hydrocarbons from bitumen containing sands. The described bioprocess can work with existing petroleum recovery protocols. The consortium microorganisms are also useful for treatment of above oil sands, ground waste tailings, subsurface oil recovery, and similar materials to enhance remediation and/or recovery of additional hydrocarbons from the materials.

  3. Study of alumosilicate porcelains: Sol-gel preparation, characterization and erosion evaluated by gravimetric method

    SciTech Connect

    Bogdanoviciene, Irma; Jankeviciute, Audrone; Pinkas, Jiri; Beganskiene, Aldona; Kareiva, Aivaras

    2008-11-03

    In this paper, the sol-gel synthesis and characteristic properties of kalsilite-type alumosilicates (KAlSiO{sub 4} and K{sub 0.5}Na{sub 0.5}AlSiO{sub 4}) are reported. The polycrystalline powders were characterized by thermal analysis (TG/DTA), powder X-ray diffraction analysis (XRD) and scanning electron microscopy (SEM). Single-phase kalsilite oxides have been obtained after annealing precursor gels for 5 h in the temperature range of 750-850 deg. C. It was demonstrated that crystallinity of the samples slightly depends on the temperature of annealing. From the results obtained, it could be concluded that the KAlSiO{sub 4} solids are composed of the volumetric plate-like grains with no regular size (from 5 {mu}m to 30 {mu}m at 750 deg. C and around 5-50 {mu}m at 850 deg. C). Larger crystallites for mixed potassium-sodium kalsilite have formed (from 10 {mu}m to 80 {mu}m at 750 deg. C and >100 {mu}m at 850 deg. C) in comparison with potassium kalsilite samples). The erosion of obtained dental porcelain samples stored in saliva, beer and Coca-Cola was compared.

  4. Aerosols concentration in the Candiota area applying different gravimetric methods of sampling and numeric modelling.

    PubMed

    Braga, C F; Alves, R C M; Teixeira, E C; Pire, M

    2002-12-01

    The main purpose of the present work is to study the concentration of atmospheric particles in the Candiota region, in the state of Rio Grande do Sul, where the Presidente Médici coal power plant is located. Aerosol samples were collected at the studied locations between December 2000 and December 2001 during 24 h periods at 15 day intervals using HV PM10 and dichotomous samplers. Then, the values obtained with the ISCST (Industrial Source Complex Term) model, with the HV PM10 sampler at all studied stations, and with the dichotomous sampler at the 8 de Agosto station were compared with each other. The results show that the values for the model had been underestimated in relation to the HV PM10 data for the studied stations, but agreed with the values obtained with the dichotomous sampler.

  5. Uncertainty estimates for the gravimetric primary flow standards of the MRF

    SciTech Connect

    Park, J.T.; Behring, K.A. II; Grimley, T.A.

    1995-12-31

    Two gravimetric flow standards for mass flowrate are in operation for the calibration of high capacity flowmeters with natural gas. Both systems measure mass electronically from scales which operate on a gyroscopic principle. The gravimetric provers are an integral part of the Gas Research Institute (GRI) Metering Research Facility (MRF) and can provide a direct primary calibration for any conventional gas flowmeter. The smaller system is attached to the Low Pressure Loop (LPL) with an operating pressure of 0.14 to 1.4 MPa (20 to 200 psia) and a flowrate up to 4.6 kg/s (10 lbm/s). The larger system is connected to the High Pressure Loop (HPL) with pressures of 1.4 to 10 MPa (200 to 1,455 psia) and flows to 43 kg/s (95 lbm/s). The performance of these two standards and their estimated uncertainties are described. The optimal total uncertainty in mass flowrate is {plus_minus}0.01% and {plus_minus}0.02%, respectively, for the LPL and HPL. The actual uncertainty is dependent on the operating conditions and is primarily a function of the operating pressure and flowrate. Uncertainty estimates are provided on the calibration of turbine meters and sonic nozzles. The largest uncertainty in the calibration of flowmeters is the uncertainty in theoretical models for density and the measurement of natural gas composition.

  6. Hyphenation of Raman spectroscopy with gravimetric analysis to interrogate water-solid interactions in pharmaceutical systems.

    PubMed

    Gift, Alan D; Taylor, Lynne S

    2007-01-01

    A moisture sorption gravimetric analyzer has been combined with a Raman spectrometer to better understand the various modes of water-solid interactions relevant to pharmaceutical systems. A commercial automated moisture sorption balance was modified to allow non-contact monitoring of the sample properties by interfacing a Raman probe with the sample holder. This hybrid instrument allows for gravimetric and spectroscopic changes to be monitored simultaneously. The utility of this instrument was demonstrated by investigating different types of water-solid interactions including stoichiometric and non-stoichiometric hydrate formation, deliquescence, amorphous-crystalline transformation, and capillary condensation. In each of the model systems, sulfaguanidine, cromolyn sodium, ranitidine HCl, amorphous sucrose and silica gel, spectroscopic changes were observed during the time course of the moisture sorption profile. Analysis of spectroscopic data provided information about the origin of the observed changes in moisture content as a function of relative humidity. Furthermore, multivariate data analysis techniques were employed as a means of processing the spectroscopic data. Principle components analysis was found to be useful to aid in data processing, handling and interpretation of the spectral changes that occurred during the time course of the moisture sorption profile.

  7. A new technique to assess dermal absorption of volatile chemicals in vitro by thermal gravimetric analysis.

    PubMed

    Rauma, Matias; Isaksson, Tina S; Johanson, Gunnar

    2006-10-01

    Potential health hazards of dermal exposure, variability in reported dermal absorption rates and potential losses from the skin by evaporation indicate a need for a simple, inexpensive and standardized procedure to measure dermal absorption and desorption of chemical substances. The aim of this study was to explore the possibility to measure dermal absorption and desorption of volatile chemicals using a new gravimetric technique, namely thermal gravimetric analysis (TGA), and trypsinated stratum corneum from pig. Changes in skin weight were readily detected before, during and after exposure to vapours of water, 2-propanol, methanol and toluene. The shape and height of the weight curves differed between the four chemicals, reflecting differences in diffusivity and partial pressure and skin:air partitioning, respectively. As the skin weight is highly sensitive to the partial pressure of volatile chemicals, including water, this technique requires carefully controlled conditions with respect to air flow, temperature, chemical vapour generation and humidity. This new technique may help in the assessment of dermal uptake of volatile chemicals. Only a small piece of skin is needed and skin integrity is not necessary, facilitating the use of human samples. The high resolution weight-time curves obtained may also help to elucidate the characteristics of absorption, desorption and diffusion of chemicals in skin.

  8. Comparative gravimetric wear analysis in mobile versus fixed-bearing posterior stabilized total knee prostheses.

    PubMed

    Delport, Hendrik P; Sloten, Jos Vander; Bellemans, Johan

    2010-06-01

    Polyethylene (PE) wear is the limiting factor for the longevity of a conventional total knee arthroplasty (TKA). Excessive wear leads to loosening and eventual implant failure. The aim of our in vitro study was to investigate wear of a PE tibial insert on a rotating platform as compared to the same insert fixed to the tibial baseplate and articulating with a similar femoral component. All tests were performed at Endolab Laboratories, Rosenheim, Germany using a knee joint simulator following ISO 14243-1. Three specific configurations were tested and compared to a loaded soak control: (1) the rotating platform using machined polyethylene (PE), (2) fixed bearing using machined PE, (3) fixed bearing using compression-moulded PE. Calf serum with a high protein concentration of 30 g/l was chosen as test lubricant. PE wear was measured gravimetrically using the ISO 14243-2 protocol. The total wear rates found for all systems tested were low. The mean wear rate was 1.40 mg per million cycles for the moulded fixed bearing, 4.07 mg per million cycles for the machined fixed bearing type and 0.82 mg per million cycles for the machined rotating platform bearing type. We conclude that the TKA system we tested (Performance, Biomet, Warsaw, IND, USA) demonstrated very low gravimetric wear. The wear rate of the same implant in the fixed mode compared to the rotating platform mode was four times higher.

  9. A kinetic study of pyrolysis and combustion of microalgae Chlorella vulgaris using thermo-gravimetric analysis.

    PubMed

    Agrawal, Ankit; Chakraborty, Saikat

    2013-01-01

    This work uses thermo-gravimetric, differential thermo-gravimetric and differential thermal analyses to evaluate the kinetics of pyrolysis (in inert/N(2) atmosphere) and (oxidative) combustion of microalgae Chlorella vulgaris by heating from 50 to 800 °C at heating rates of 5-40 °C/min. This study shows that combustion produces higher biomass conversion than pyrolysis, and that three stages of decomposition occur in both cases, of which, the second one--consisting of two temperature zones--is the main stage of devolatization. Proteins and carbohydrates are decomposed in the first of the two zones at activation energies of 51 and 45 kJ/mol for pyrolysis and combustion, respectively, while lipids are decomposed in its second zone at higher activation energies of 64 and 63 kJ/mol, respectively. The kinetic expressions of the reaction rates in the two zones for pyrolysis and combustion have been obtained and it has been shown that increased heating rates result in faster and higher conversion.

  10. Comparison of polar motion excitation functions computed from different sets of gravimetric coefficients

    NASA Astrophysics Data System (ADS)

    Nastula, J.; Winska, M.; Birylo, M.

    2015-08-01

    Since its launch in February, the Gravity Recovery and Climate Experiment (GRACE) has been source of data of temporal changes in Earth's gravity field. These gravity fields can be used to determine the changing mass field of the Earth caused by redistribution of the geophysical fluids, and from that excitations of polar motion. The so-called Level 2 gravity field product are available, in the form of changes in the coefficients: C_{nm}, S_{nm}. Since 2002 until the present time there are still attempts to better process these data. In this study we estimate gravimetric excitation of polar motion using a recent series of C_{21}, S_{21} coefficients. In our calculations we use several series developed by different centers. Firstly, we compare these gravimetric functions with each other. Then we examine the compatibility of these functions with hydrological signal in observed geodetic excitation function. We focus on seasonal and subseasonal time scales. The main purpose is to explore which from these several solutions are closed.

  11. Least squares collocation applied to local gravimetric solutions from satellite gravity gradiometry data

    NASA Technical Reports Server (NTRS)

    Robbins, J. W.

    1985-01-01

    An autonomous spaceborne gravity gradiometer mission is being considered as a post Geopotential Research Mission project. The introduction of satellite diometry data to geodesy is expected to improve solid earth gravity models. The possibility of utilizing gradiometer data for the determination of pertinent gravimetric quantities on a local basis is explored. The analytical technique of least squares collocation is investigated for its usefulness in local solutions of this type. It is assumed, in the error analysis, that the vertical gravity gradient component of the gradient tensor is used as the raw data signal from which the corresponding reference gradients are removed to create the centered observations required in the collocation solution. The reference gradients are computed from a high degree and order geopotential model. The solution can be made in terms of mean or point gravity anomalies, height anomalies, or other useful gravimetric quantities depending on the choice of covariance types. Selected for this study were 30 x 30 foot mean gravity and height anomalies. Existing software and new software are utilized to implement the collocation technique. It was determined that satellite gradiometry data at an altitude of 200 km can be used successfully for the determination of 30 x 30 foot mean gravity anomalies to an accuracy of 9.2 mgal from this algorithm. It is shown that the resulting accuracy estimates are sensitive to gravity model coefficient uncertainties, data reduction assumptions and satellite mission parameters.

  12. Comparison of two extraction methods for the analysis of petroleum hydrocarbon residues in mallard duck eggs by GC and GC-MS

    USGS Publications Warehouse

    Belisle, A.A.; Gay, M.L.; Coon, N.C.

    1981-01-01

    Hydrocarbon residues in pooled eggs from a mallard duck on a diet of 25,000 ppm South Louisiana crude oil were compared after cleanup with and without saponification. The saponification procedure yielded superior reproducibility and extraction efficiency

  13. Comparison of two extraction methods for the analysis of petroleum hydrocarbon residues in mallard duck eggs by GC and GC-MS. [NONE

    SciTech Connect

    Belisle, A.A.; Gay, M.L.; Coon, N.C.

    1981-01-01

    Hydrocarbon residues in pooled eggs from a mallard duck on a diet of 25,000 ppm South Louisiana crude oil were compared after cleanup with and without saponification. The saponification procedure yielded superior reproducibility and extraction efficiency..

  14. Multiple zone catalytic cracking of hydrocarbons

    SciTech Connect

    Harandi, M.N.; Owen, H.

    1992-10-13

    This patent describes a method of cracking a heavy hydrocarbon feedstock and a light hydrocarbon feedstock in a riser reactor, the method producing spent catalyst and regenerated catalyst, the spent and regeneration catalyst comprising a large pore size aluminosilicate zeolite cracking catalyst selected form zeolite Y or USY. It comprises: contacting the light hydrocarbon feedstock with spent catalyst at an initial contact location in the riser; passing a suspension comprising the light hydrocarbon feedstock and the spent catalyst through the riser; introducing the heavy hydrocarbon feedstock into the suspension at a second location downstream of the initial contact location; and introducing the regenerated catalyst into the suspension at a location in the riser downstream of the initial contact location.

  15. Assessment of factors influencing PM mass concentration measured by gravimetric & beta attenuation techniques at a suburban site

    NASA Astrophysics Data System (ADS)

    Triantafyllou, E.; Diapouli, E.; Tsilibari, E. M.; Adamopoulos, A. D.; Biskos, G.; Eleftheriadis, K.

    2016-04-01

    Near real-time atmospheric particulate matter (PM) monitors are extensively used in air quality networks given their ability to provide continuous measurements with minimal attention by the operator. Their principle of operation is based on measurement of a physical parameter that is quantitatively linked to the PM mass concentration. Significant discrepancies between these measurements and those obtained by the reference gravimetric method, conducted in regions with diverse climatic conditions, have been reported in the literature. In this study we compare systematic PM2.5 and PM10 gravimetric (GM) and beta attenuation (BA) measurements performed at a suburban site in Athens, Greece, over a period of 4 years (2009-2012). In general, BA and GM datasets exhibited similar temporal variation for both PM size fractions. An overestimation of the ΒΑ measurements, which was ∼30% for the PM2.5 and ∼10% for the PM10 data, was observed. Good linear correlations between GM and BA data were observed, with estimated Pearson coefficients being 0.79 for the PM2.5 and 0.85 for the PM10 measurements. The respective fitted equations through the entire dataset were BA = 0.71 GM + 6.2, and BA = 0.77 G M + 4.1. Better correlation between GM and BA measurements was observed during the cold rather than the warm period. Discrepancies between BA and GM PM2.5 measurements increased with increasing available water vapor, suggesting that the aerosol bound water has a strong effect on the measurements. The effect of filter material used for GM measurements (i.e., quartz, glass fiber, or Teflon) was also examined for the PM2.5 dataset. Best correlation between BA and GM data was observed when glass fiber, which is incidentally the material of the BA filter tape, was used in the GM measurements. When the BA to GM relationship was examined by further categorizing the data by the season (i.e., cold and warm period) for different filter types, the relationships that were fitted to the data

  16. Isolation and Characterization of Hydrocarbon-Degrading Yeast Strains from Petroleum Contaminated Industrial Wastewater

    PubMed Central

    Gargouri, Boutheina; Mhiri, Najla; Karray, Fatma; Aloui, Fathi; Sayadi, Sami

    2015-01-01

    Two yeast strains are enriched and isolated from industrial refinery wastewater. These strains were observed for their ability to utilize several classes of petroleum hydrocarbons substrates, such as n-alkanes and aromatic hydrocarbons as a sole carbon source. Phylogenetic analysis based on the D1/D2 variable domain and the ITS-region sequences indicated that strains HC1 and HC4 were members of the genera Candida and Trichosporon, respectively. The mechanism of hydrocarbon uptaking by yeast, Candida, and Trichosporon has been studied by means of the kinetic analysis of hydrocarbons-degrading yeasts growth and substrate assimilation. Biodegradation capacity and biomass quantity were daily measured during twelve days by gravimetric analysis and gas chromatography coupled with mass spectrometry techniques. Removal of n-alkanes indicated a strong ability of hydrocarbon biodegradation by the isolated yeast strains. These two strains grew on long-chain n-alkane, diesel oil, and crude oil but failed to grow on short-chain n-alkane and aromatic hydrocarbons. Growth measurement attributes of the isolates, using n-hexadecane, diesel oil, and crude oil as substrates, showed that strain HC1 had better degradation for hydrocarbon substrates than strain HC4. In conclusion, these yeast strains can be useful for the bioremediation process and decreasing petroleum pollution in wastewater contaminated with petroleum hydrocarbons. PMID:26339653

  17. Isolation and Characterization of Hydrocarbon-Degrading Yeast Strains from Petroleum Contaminated Industrial Wastewater.

    PubMed

    Gargouri, Boutheina; Mhiri, Najla; Karray, Fatma; Aloui, Fathi; Sayadi, Sami

    2015-01-01

    Two yeast strains are enriched and isolated from industrial refinery wastewater. These strains were observed for their ability to utilize several classes of petroleum hydrocarbons substrates, such as n-alkanes and aromatic hydrocarbons as a sole carbon source. Phylogenetic analysis based on the D1/D2 variable domain and the ITS-region sequences indicated that strains HC1 and HC4 were members of the genera Candida and Trichosporon, respectively. The mechanism of hydrocarbon uptaking by yeast, Candida, and Trichosporon has been studied by means of the kinetic analysis of hydrocarbons-degrading yeasts growth and substrate assimilation. Biodegradation capacity and biomass quantity were daily measured during twelve days by gravimetric analysis and gas chromatography coupled with mass spectrometry techniques. Removal of n-alkanes indicated a strong ability of hydrocarbon biodegradation by the isolated yeast strains. These two strains grew on long-chain n-alkane, diesel oil, and crude oil but failed to grow on short-chain n-alkane and aromatic hydrocarbons. Growth measurement attributes of the isolates, using n-hexadecane, diesel oil, and crude oil as substrates, showed that strain HC1 had better degradation for hydrocarbon substrates than strain HC4. In conclusion, these yeast strains can be useful for the bioremediation process and decreasing petroleum pollution in wastewater contaminated with petroleum hydrocarbons.

  18. Hydrocarbon components in carbonaceous meteorites

    NASA Astrophysics Data System (ADS)

    Kissin, Y. V.

    2003-05-01

    Currently, the presence of free n-alkanes and isoprenoid alkanes in carbonaceous meteorites is usually explained either by microbial contamination during the period between the meteorite fall and collection or by contamination from the environment of analytical laboratories and museums. The goal of this research was to repeat analysis of hydrocarbon components in meteorites and to investigate possible meteorite contamination routes discussed in the literature. Experimental analysis of free organic constituents in five carbonaceous meteorites by infrared spectroscopy (IR) and gas chromatographic (GC) methods confirmed the presence of extractable aliphatic components, n-alkanes in the C 15H 32-C 27H 56 range and isoprenoid alkanes (phytane, pristane, and norpristane), in some of these meteorites. The contents of these compounds vary depending on the source. Insoluble organic components of two meteorites (meteorite kerogens) were isolated, and their composition was analyzed by IR and cracking/GC methods. Comparison with the data on several terrestrial contamination sources proposed in the literature shows that the presence of free saturated hydrocarbons in meteorites and the composition of the meteorite kerogen could not be explained either by microbial contamination or by contamination from the laboratory environment. The types of the hydrocarbons in meteorites resemble those typical of ancient terrestrial deposits of organic-rich sediments, except for the absence of lighter hydrocarbons, which apparently slowly evaporated in space, and multi-ring naphthenic compounds of the biologic origin, steranes, terpanes, etc. The prevailing current explanation for the presence of free linear saturated hydrocarbons in carbonaceous meteorites, apart from contamination, is the abiotic route from hydrogen and carbon monoxide. However, the data on the structure of meteorite kerogens require a search for different routes that initially produce complex polymeric structures containing

  19. Ether and hydrocarbon production

    SciTech Connect

    Harandi, M.N.; Owen, H.

    1991-03-19

    This patent describes a continuous process for converting lower aliphatic alkanol and olefinic hydrocarbon to alkyl tertiary-alkyl ethers and C{sub 5} + gasoline boiling range hydrocarbons. It comprises contacting alkanol and a light olefinic hydrocarbon stream rich in isobutylene and other C{sub 4} isomeric hydrocarbons under iso-olefin etherification conditions in an etherification reaction zone containing acid etherification catalyst; separating etherification effluent to recover a light stream comprising unreacted alkanol and light olefinic hydrocarbon and a liquid product stream containing alkyl tertiary-butyl ether; and contacting the light stream with acidic, medium pore metallosilicate catalyst under alkanol and hydrocarbon conversion conditions whereby C{sub 5} + gasoline boiling range hydrocarbons are produced.

  20. Development of new method of δ(13)C measurement for trace hydrocarbons in natural gas using solid phase micro-extraction coupled to gas chromatography isotope ratio mass spectrometry.

    PubMed

    Li, Zhongping; Wang, Xibin; Li, Liwu; Zhang, Mingjie; Tao, Mingxin; Xing, Lantian; Cao, Chunhui; Xia, Yanqing

    2014-11-01

    Compound specific isotope analysis (CSIA) of normal-level hydrocarbons (C1-C4) in natural gas is often successfully used in natural gas origin identification and classification, but little progress so far has been made for trace level hydrocarbons (C5-C14) in natural gas. In this study, we developed a method for rapid analysis of carbon isotopic ratios for trace hydrocarbons in natural gas samples. This method can be described as a combined approach characterized by solid phase micro-extraction (SPME) technique coupled to gas chromatography isotope ratio mass spectrometry (GC/IRMS). In this study, the CAR-PDMS fiber was chosen as the SPME adsorptive material after comparative experiments with other four fibers, and the parameters, including equilibration time, extraction temperature and desorption time, for efficient extraction of trace hydrocarbons were systematically optimized. The results showed the carbon isotopic fractionation was not observed as a function of equilibration time and extraction temperature. And the δ(13)C signatures determined by SPME-GC/IRMS were in good agreement with the known δ(13)C values of C5-C14 measured by GC-IRMS, and the accuracy is generally within ±0.5‰. Five natural gas samples were analyzed using this method, and the δ(13)C values for C5-C14 components were obtained with satisfied repeatability. The SPME-GC/IRMS approach fitted with CAR-PDMS fiber is well suited for the preconcentration of trace hydrocarbons and provides so far the most reliable carbon isotopic analysis for trace compounds in natural gas. PMID:25465020

  1. Development of new method of δ(13)C measurement for trace hydrocarbons in natural gas using solid phase micro-extraction coupled to gas chromatography isotope ratio mass spectrometry.

    PubMed

    Li, Zhongping; Wang, Xibin; Li, Liwu; Zhang, Mingjie; Tao, Mingxin; Xing, Lantian; Cao, Chunhui; Xia, Yanqing

    2014-11-01

    Compound specific isotope analysis (CSIA) of normal-level hydrocarbons (C1-C4) in natural gas is often successfully used in natural gas origin identification and classification, but little progress so far has been made for trace level hydrocarbons (C5-C14) in natural gas. In this study, we developed a method for rapid analysis of carbon isotopic ratios for trace hydrocarbons in natural gas samples. This method can be described as a combined approach characterized by solid phase micro-extraction (SPME) technique coupled to gas chromatography isotope ratio mass spectrometry (GC/IRMS). In this study, the CAR-PDMS fiber was chosen as the SPME adsorptive material after comparative experiments with other four fibers, and the parameters, including equilibration time, extraction temperature and desorption time, for efficient extraction of trace hydrocarbons were systematically optimized. The results showed the carbon isotopic fractionation was not observed as a function of equilibration time and extraction temperature. And the δ(13)C signatures determined by SPME-GC/IRMS were in good agreement with the known δ(13)C values of C5-C14 measured by GC-IRMS, and the accuracy is generally within ±0.5‰. Five natural gas samples were analyzed using this method, and the δ(13)C values for C5-C14 components were obtained with satisfied repeatability. The SPME-GC/IRMS approach fitted with CAR-PDMS fiber is well suited for the preconcentration of trace hydrocarbons and provides so far the most reliable carbon isotopic analysis for trace compounds in natural gas.

  2. The accumulation of polycyclic aromatic hydrocarbons in lubricating oil over time--a comparison of supercritical fluid and liquid-liquid extraction methods.

    PubMed

    Wong, P K; Wang, J

    2001-01-01

    Optimal extraction conditions including extraction temperature, fluid density of carbon dioxide and concentration of modifier for supercritical fluid extraction (SFE) to extract of 16 2-6-ring polycyclic aromatic hydrocarbons (PAHs) spiked into used lubricating oil collected from a gasoline-driven automobile were determined. A comparison of extraction efficiency 2-6-ring PAHs spiked into the used lubricating oil extracted by SFE and liquid-liquid extraction (LLE) methods was made. Results indicated that recoveries of PAHs extracted by SFE from the used lubricating oil were higher than those by LLE. PAH profiles of lubricating oil samples collected at various driving distances from an old and a new gasoline-driven automobiles were determined by combining SFE, gel permeation chromatography clean up and gas chromatography-mass spectrometry analysis. Results showed that the concentrations of total PAH in lubricating oils collected from both automobiles increased rapidly after oil change. Two- and three-ring PAHs dominated the PAH profiles of oil samples collected from both automobiles. High concentrations of the more toxic 4-6-ring PAHs, were found in the oil samples collected from both automobiles even at a short driving distance after oil change. The concentrations of total PAH in lubricating oil collected from two automobiles driven for a longer distance after oil change were very similar.

  3. The accumulation of polycyclic aromatic hydrocarbons in lubricating oil over time--a comparison of supercritical fluid and liquid-liquid extraction methods.

    PubMed

    Wong, P K; Wang, J

    2001-01-01

    Optimal extraction conditions including extraction temperature, fluid density of carbon dioxide and concentration of modifier for supercritical fluid extraction (SFE) to extract of 16 2-6-ring polycyclic aromatic hydrocarbons (PAHs) spiked into used lubricating oil collected from a gasoline-driven automobile were determined. A comparison of extraction efficiency 2-6-ring PAHs spiked into the used lubricating oil extracted by SFE and liquid-liquid extraction (LLE) methods was made. Results indicated that recoveries of PAHs extracted by SFE from the used lubricating oil were higher than those by LLE. PAH profiles of lubricating oil samples collected at various driving distances from an old and a new gasoline-driven automobiles were determined by combining SFE, gel permeation chromatography clean up and gas chromatography-mass spectrometry analysis. Results showed that the concentrations of total PAH in lubricating oils collected from both automobiles increased rapidly after oil change. Two- and three-ring PAHs dominated the PAH profiles of oil samples collected from both automobiles. High concentrations of the more toxic 4-6-ring PAHs, were found in the oil samples collected from both automobiles even at a short driving distance after oil change. The concentrations of total PAH in lubricating oil collected from two automobiles driven for a longer distance after oil change were very similar. PMID:11291447

  4. A highly accurate absolute gravimetric network for Albania, Kosovo and Montenegro

    NASA Astrophysics Data System (ADS)

    Ullrich, Christian; Ruess, Diethard; Butta, Hubert; Qirko, Kristaq; Pavicevic, Bozidar; Murat, Meha

    2016-04-01

    The objective of this project is to establish a basic gravity network in Albania, Kosovo and Montenegro to enable further investigations in geodetic and geophysical issues. Therefore the first time in history absolute gravity measurements were performed in these countries. The Norwegian mapping authority Kartverket is assisting the national mapping authorities in Kosovo (KCA) (Kosovo Cadastral Agency - Agjencia Kadastrale e Kosovës), Albania (ASIG) (Autoriteti Shtetëror i Informacionit Gjeohapësinor) and in Montenegro (REA) (Real Estate Administration of Montenegro - Uprava za nekretnine Crne Gore) in improving the geodetic frameworks. The gravity measurements are funded by Kartverket. The absolute gravimetric measurements were performed from BEV (Federal Office of Metrology and Surveying) with the absolute gravimeter FG5-242. As a national metrology institute (NMI) the Metrology Service of the BEV maintains the national standards for the realisation of the legal units of measurement and ensures their international equivalence and recognition. Laser and clock of the absolute gravimeter were calibrated before and after the measurements. The absolute gravimetric survey was carried out from September to October 2015. Finally all 8 scheduled stations were successfully measured: there are three stations located in Montenegro, two stations in Kosovo and three stations in Albania. The stations are distributed over the countries to establish a gravity network for each country. The vertical gradients were measured at all 8 stations with the relative gravimeter Scintrex CG5. The high class quality of some absolute gravity stations can be used for gravity monitoring activities in future. The measurement uncertainties of the absolute gravity measurements range around 2.5 micro Gal at all stations (1 microgal = 10-8 m/s2). In Montenegro the large gravity difference of 200 MilliGal between station Zabljak and Podgorica can be even used for calibration of relative gravimeters

  5. Relationship between gravimetric wear and particle generation in hip simulators: conventional compared with cross-linked polyethylene.

    PubMed

    Ries, M D; Scott, M L; Jani, S

    2001-01-01

    Hip-simulator studies have shown reduced gravimetric wear rates for inert-gas gamma-irradiated ultra-high molecular weight polyethylene when compared with conventional ethylene-oxide-sterilized ultra-high molecular weight polyethylene. Analysis shows a greater number of particles generated from inert-gas gamma-irradiated ultra-high molecular weight polyethylene. This study was undertaken to examine particle-generation rates of polyethylene with different levels of cross-linking and to correlate them with gravimetric wear data. Particle-generation rates did not correlate with gravimetric wear rates. Particle analysis should be performed to predict the in vivo behavior of bearing surface materials. Cross-linked ultra-high molecular weight polyethylene subjected to 10 Mrad (100,000 Gy) of gamma irradiation generated significantly fewer particles than ethylene-oxide-sterilized ultra-high molecular weight polyethylene; it also demonstrated a 96% reduction in the volume of particles.

  6. Utilization of an ionic liquid in situ preconcentration method for the determination of the 15 + 1 European Union polycyclic aromatic hydrocarbons in drinking water and fruit-tea infusions.

    PubMed

    Germán-Hernández, Mónica; Crespo-Llabrés, Pilar; Pino, Verónica; Ayala, Juan H; Afonso, Ana M

    2013-08-01

    An ionic liquid (IL) in situ preconcentration method was optimized and applied to the monitoring of the 15 + 1 European Union polycyclic aromatic hydrocarbons in water and fruit-tea infusions. The optimized method utilizes 10 mL of water (or infusion) containing 38 μL of the IL 1-butyl-3-methylimidazolium chloride and a content of 36.1 g/L NaCl, which are mixed with Li-NTf2 (340 μL, 0.2 g/mL), followed by vortex (4 min) and centrifugation (5 min). The obtained microdroplet containing hydrocarbons is diluted with acetonitrile and injected into an HPLC with UV/Vis and fluorescence detection. The method presented average enrichment factors of 127 for water (tap water and bottled water) and 27 for two fruit-tea infusions; with average relative recoveries of 86.7 and 106% for water and fruit-tea infusions, respectively. The method was sensitive, with detection limits ranging from 0.001 to 0.050 ng/mL in water, and from 0.010 to 0.600 ng/mL in fruit-tea infusions, for the fluorescent hydrocarbons. Real extraction efficiencies ranged from 12.7 to 58.7% for water, and from 20.2 to 117% for the infusions. The method was also fast (~12 min) and free of organic solvents in the extraction step.

  7. Hydrocarbon distribution in the Maracaibo Basin

    SciTech Connect

    Scherer, W.

    1996-08-01

    The prolific Maracaibo basin contains the second largest hydrocarbon accumulation in South America; it has been one of the principal oil producers of the world since the beginning of this century. Exploratory efforts in this basin, carried out with new techniques and new ideas, continue today, so it is of interest to determine the trends of hydrocarbon concentrations in terms of resources per unit volume of sediments and to correlate them to stratigraphic, sedimentary-tectonic and geochemical variables. Regional scale maps representing the 24 principal geologic and geochemical variables that are thought to be a function of hydrocarbon generation, migration and accumulation were discretized on a 25 x 25 km grid. Variables used are isopach and Total Organic Carbon (TOC) of source rocks, isopach, sandstone content and grain size parameters of reservoir rocks, isopach of stratigraphic seal and overburden, maximum paleotemperatures (R{sub o} and T{sub max}), tectonic energy (fault length and displacement) and hydrocarbon families. Multivariate analytical statistics was used to obtain the trends of hydrocarbon distributions. The resulting hydrocarbon concentration trend map was quantitatively correlated to known hydrocarbon accumulations and prospective areas, where additional new accumulations might be found, were obtained. It can be shown that the largest known hydrocarbon concentrations correspond to areas of greatest cumulative overburden. The southern Zulia Catatumbo region is the largest prospective area determined by this method.

  8. Single-laboratory validation of a GC/MS method for the determination of 27 polycyclic aromatic hydrocarbons (PAHs) in oils and fats.

    PubMed

    Rose, M; White, S; Macarthur, R; Petch, R G; Holland, J; Damant, A P

    2007-06-01

    A protocol for the measurement of 27 polycyclic aromatic hydrocarbons (PAHs) in vegetable oils by GC/MS has undergone single-laboratory validation. PAHs were measured in three oils (olive pomace, sunflower and coconut oil). Five samples of each oil (one unfortified, and four fortified at concentrations between 2 and 50 microg kg(-1)) were analysed in replicate (four times in separate runs). Two samples (one unfortified and one fortified at 2 microg kg(-1)) of five oils (virgin olive oil, grapeseed oil, toasted sesame oil, olive margarine and palm oil) were also analysed. The validation included an assessment of measurement bias from the results of 120 measurements of a certified reference material (coconut oil BCR CRM458 certified for six PAHs). The method is capable of reliably detecting 26 out of 27 PAHs, at concentration <2 microg kg(-1) which is the European Union maximum limit for benzo[a]pyrene, in vegetable oils, olive pomace oil, sunflower oil and coconut oil. Quantitative results were obtained that are fit for purpose for concentrations from <2 to 50 microg kg(-1) for 24 out of 27 PAHs in olive pomace oil, sunflower oil and coconut oil. The reliable detection of 2 microg kg(-1) of PAHs in five additional oils (virgin olive oil, grapeseed oil, toasted sesame oil, olive margarine and palm oil) has been demonstrated. The method failed to produce fit-for-purpose results for the measurement of dibenzo[a,h]pyrene, anthanthrene and cyclopenta[c,d]pyrene. The reason for the failure was the large variation in results. The likely cause was the lack of availability of (13)C isotope internal standards for these PAHs at the time of the study. The protocol has been shown to be fit-for-purpose and is suitable for formal validation by inter-laboratory collaborative study. PMID:17487605

  9. Using supercritical fluids to refine hydrocarbons

    DOEpatents

    Yarbro, Stephen Lee

    2015-06-09

    A system and method for reactively refining hydrocarbons, such as heavy oils with API gravities of less than 20 degrees and bitumen-like hydrocarbons with viscosities greater than 1000 cp at standard temperature and pressure, using a selected fluid at supercritical conditions. A reaction portion of the system and method delivers lightweight, volatile hydrocarbons to an associated contacting unit which operates in mixed subcritical/supercritical or supercritical modes. Using thermal diffusion, multiphase contact, or a momentum generating pressure gradient, the contacting unit separates the reaction products into portions that are viable for use or sale without further conventional refining and hydro-processing techniques.

  10. Nonisothermal gravimetric investigation on kinetics of reduction of magnesia by aluminum

    SciTech Connect

    Hong, L.; Okumura, Keiji; Sano, Masamichi

    1999-12-01

    An investigation of the reduction of magnesia by aluminum was carried out using a nonisothermal gravimetric technique under an argon atmosphere, in the temperature range from 1,273 to 1,873 K. The mixture of magnesia and aluminum powders was formed into a pellet under various isostatic pressures. It was found that magnesia is reduced by aluminum to form magnesium and spinel at first, and then the excess aluminum reacts with spinel slowly. The temperature at which the reaction starts increases with an increasing heating rate. The reaction rate is also affected by pellet-forming conditions. A kinetic model is proposed to explain the experimental results. The activation energy of the reduction of magnesia by aluminum is 151.2 kJ/mol. Good agreement between calculated and experimental results is obtained.

  11. A micrographic and gravimetric study of intercalation and deintercalation of graphite fibers

    NASA Technical Reports Server (NTRS)

    Hung, C. C.

    1985-01-01

    Intercalation and deintercalation of Union Carbide P-100 graphite fibers with liquid and vaporous bromine was studied gravimetrically and microscopically. The mass of the bromine intercalated fibers was found to be 17 to 20 percent greater than their pristine counterpart. This variation decreased to 17 to 18 percent after heating in air for 3 days at 200 C and to 14.5 to 18 percent after 6 days of 260 C heating. The fiber length did not change throughout the experiment. The fiber diameter increased during intercalation and decreased slightly upon deintercalation but was not affected by heating to 260 C for 3 days in air. Comparing the mass and volume data to those with highly oriented pyrolitic graphite or natural single crystal graphite suggested the possibility that the intercalated P-100 fibers could be mostly stage 4.

  12. Global detailed gravimetric geoid. [based on gravity model derived from satellite tracking and surface gravity data

    NASA Technical Reports Server (NTRS)

    Vincent, S.; Marsh, J. G.

    1973-01-01

    A global detailed gravimetric geoid has been computed by combining the Goddard Space Flight Center GEM-4 gravity model derived from satellite and surface gravity data and surface 1 deg-by-1 deg mean free air gravity anomaly data. The accuracy of the geoid is + or - 2 meters on continents, 5 to 7 meters in areas where surface gravity data are sparse, and 10 to 15 meters in areas where no surface gravity data are available. Comparisons have been made with the astrogeodetic data provided by Rice (United States), Bomford (Europe), and Mather (Australia). Comparisons have also been carried out with geoid heights derived from satellite solutions for geocentric station coordinates in North America, the Caribbean, Europe, and Australia.

  13. Catalytic conversion of alcohols to hydrocarbons with low benzene content

    DOEpatents

    Narula, Chaitanya K.; Davison, Brian H.; Keller, Martin

    2016-03-08

    A method for converting an alcohol to a hydrocarbon fraction having a lowered benzene content, the method comprising: converting said alcohol to a hydrocarbon fraction by contacting said alcohol, under conditions suitable for converting said alcohol to said hydrocarbon fraction, with a metal-loaded zeolite catalyst catalytically active for converting said alcohol to said hydrocarbon fraction, and contacting said hydrocarbon fraction with a benzene alkylation catalyst, under conditions suitable for alkylating benzene, to form alkylated benzene product in said hydrocarbon fraction. Also described is a catalyst composition useful in the method, comprising a mixture of (i) a metal-loaded zeolite catalyst catalytically active for converting said alcohol to said hydrocarbon, and (ii) a benzene alkylation catalyst, in which (i) and (ii) may be in a mixed or separated state. A reactor for housing the catalyst and conducting the reaction is also described.

  14. Catalytic conversion of alcohols to hydrocarbons with low benzene content

    DOEpatents

    Narula, Chaitanya K.; Davison, Brian H.; Keller, Martin

    2016-09-06

    A method for converting an alcohol to a hydrocarbon fraction having a lowered benzene content, the method comprising: converting said alcohol to a hydrocarbon fraction by contacting said alcohol, under conditions suitable for converting said alcohol to said hydrocarbon fraction, with a metal-loaded zeolite catalyst catalytically active for converting said alcohol to said hydrocarbon fraction, and contacting said hydrocarbon fraction with a benzene alkylation catalyst, under conditions suitable for alkylating benzene, to form alkylated benzene product in said hydrocarbon fraction. Also described is a catalyst composition useful in the method, comprising a mixture of (i) a metal-loaded zeolite catalyst catalytically active for converting said alcohol to said hydrocarbon, and (ii) a benzene alkylation catalyst, in which (i) and (ii) may be in a mixed or separated state. A reactor for housing the catalyst and conducting the reaction is also described.

  15. The use of gravimetric data from GRACE mission in the understanding of polar motion variations

    NASA Astrophysics Data System (ADS)

    Seoane, L.; Nastula, J.; Bizouard, C.; Gambis, D.

    2009-08-01

    Tesseral coefficients C21 and S21 derived from Gravity Recovery and Climate Experiment (GRACE) observations allow to compute the mass term of the polar-motion excitation function. This independent estimation can improve the geophysical models and, in addition, determine the unmodelled phenomena. In this paper, we intend to validate the polar motion excitation derived from GRACE's last release (GRACE Release 4) computed by different institutes: GeoForschungsZentrum (GFZ), Postdam, Germany; Center for Space Research (CSR), Austin, USA; Jet Propulsion Laboratory (JPL), Pasadena, USA, and the Groupe de Recherche en Géodésie Spatiale (GRGS), Toulouse, France. For this purpose, we compare these excitations functions first to the mass term obtained from observed Earth's rotation variations free of the motion term and, second, to the mass term estimated from geophysical fluids models. We confirm the large improvement of the CSR solution, and we show that the GRGS estimate is also well correlated with the geodetic observations. Significant discrepancies exist between the solutions of each centre. The source of these differences is probably related to the data processing strategy. We also consider residuals computed after removing the geophysical models or the gravimetric solutions from the geodetic mass term. We show that the residual excitation based on models is smoother than the gravimetric data, which are still noisy. Still, they are comparable for the χ2 component. It appears that χ2 residual signals using GFZ and JPL data have less variability. Finally, for assessing the impact of the geophysical fluids models choice on our results, we checked two different oceanic excitation series. We show the significant differences in the residuals correlations, especially for the χ1 more sensitive to the oceanic signals.

  16. Deep desulfurization of hydrocarbon fuels

    DOEpatents

    Song, Chunshan; Ma, Xiaoliang; Sprague, Michael J.; Subramani, Velu

    2012-04-17

    The invention relates to processes for reducing the sulfur content in hydrocarbon fuels such as gasoline, diesel fuel and jet fuel. The invention provides a method and materials for producing ultra low sulfur content transportation fuels for motor vehicles as well as for applications such as fuel cells. The materials and method of the invention may be used at ambient or elevated temperatures and at ambient or elevated pressures without the need for hydrogen.

  17. Ultraviolet and visible spectra of the 1,3,5-trinitrobenzolates of polycyclic aromatic hydrocarbons and other organic compounds: A method for their identification (Part II)

    SciTech Connect

    Tombesi, O.L.; Frontera, M.A.; Tomas, M.A.; Badajoz, M.A. )

    1993-01-01

    In a previous paper, a study of ultraviolet and visible spectra of the picrates of polycyclic aromatic hydrocarbons and other representative organic compounds was reported. In the present paper, a similar study of 1,3,5-trinitrobenzolates derivatives is described. In the following discussion, the ultraviolet and visible spectra of the 1,3,5-trinitrobenzolates of polycyclic aromatic hydrocarbons [naphthalene (I), [beta]-methylnaphthalene (II), anthracene (III), phenanthrene (IV), chrysene (V), pyrene (VI), fluorene (VII), and acenaphthene (VIII)] and other representative organic compounds [dibenzofuran (IX), [beta]-naphthol (X), and [alpha]-naphthylamine (XI)] are given. 9 refs.

  18. Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory : determination of polycyclic aromatic hydrocarbon compounds in sediment by gas chromatography/mass spectrometry

    USGS Publications Warehouse

    Olson, Mary C.; Iverson, Jana L.; Furlong, Edward T.; Schroeder, Michael P.

    2004-01-01

    A method for the determination of 28 polycyclic aromatic hydrocarbons (PAHs) and 25 alkylated PAH homolog groups in sediment samples is described. The compounds are extracted from sediment by solvent extraction, followed by partial isolation using high-performance gel permeation chromatography. The compounds are identified and uantitated using capillary-column gas chromatography/mass spectrometry. The report presents performance data for full-scan ion monitoring. Method detection limits in laboratory reagent matrix samples range from 1.3 to 5.1 micrograms per kilogram for the 28 PAHs. The 25 groups of alkylated PAHs are homologs of five groups of isomeric parent PAHs. Because of the lack of authentic standards, these homologs are reported semiquantitatively using a response factor from a parent PAH or a specific alkylated PAH. Precision data for the alkylated PAH homologs are presented using two different standard reference manuals produced by the National Institute of Standards and Technology: SRM 1941b and SRM 1944. The percent relative standard deviations for identified alkylated PAH homolog groups ranged from 1.55 to 6.98 for SRM 1941b and from 6.11 to 12.0 for SRM 1944. Homolog group concentrations reported under this method include the concentrations of individually identified compounds that are members of the group. Organochlorine (OC) pesticides--including toxaphene, polychlorinated biphenyls (PCBs), and organophosphate (OP) pesticides--can be isolated simultaneously using this method. In brief, sediment samples are centrifuged to remove excess water and extracted overnight with dichloromethan (95 percent) and methanol (5 percent). The extract is concentrated and then filtered through a 0.2-micrometer polytetrafluoroethylene syringe filter. The PAH fraction is isolated by quantitatively injecting an aliquot of sample onto two polystyrene-divinylbenzene gel-permeation chromatographic columns connected in series. The compounds are eluted with dichloromethane

  19. Mobile Laboratory Measurements of Black Carbon and Polycyclic Aromatic Hydrocarbon Emissions in Mexico City: A New Method for Motor Vehicle Emission Inventory Calculations

    NASA Astrophysics Data System (ADS)

    Jiang, M.; Marr, L. C.; Dunlea, E.; Herndon, S.; Jayne, J.; Rogers, T.; Knighton, B.; Zavala, M.; Molina, L. T.; Molina, M. J.

    2004-12-01

    Aerosol black carbon (BC) and polycyclic aromatic hydrocarbons (PAHs) are two products of carbonaceous fuel combustion that are of major concern for urban air quality and global climate change. As part of the Mexico City Metropolitan Area field campaign in April 2003 (MCMA-2003), a mobile laboratory drove throughout the city and chased vehicles to measure pollutants in their exhaust emissions. The laboratory is a van designed and built by Aerodyne Research, Inc. and is equipped with a suite of gas and particle analyzers, including an aethalometer that measures BC and a photoemission aerosol sensor that measures particle-bound PAHs. The main goal of this research is to determine fuel-based emission factors, or the mass of BC and PAH emitted per volume of fuel burned, for Mexico City¡_s vehicle fleet. We can then calculate the megacity¡_s emission inventory of these compounds, which is important on both the urban and global scales. In previous analyses, the mobile laboratory has been used to target emissions from specific vehicles. While chasing events can be analyzed to obtain emission factors for specific vehicles, data from the entire time period while the lab is driving through the streets, whether chasing individual vehicles or not, can also provide valuable information about mobile source emissions. The laboratory continuously samples ambient air from an inlet at the front of the van, and it is always ¡°seeing¡± exhaust plumes from the vehicles around it. This ¡°macroscopic¡± approach that considers all vehicles on the road, similar to tunnel and remote sensing studies, complements the ¡°microscopic¡± approach that focuses on individual vehicles. We have developed a method that automatically identifies exhaust plumes and quantifies emission factors from data collected by the mobile lab. While 200 individual chasing events were identified during the field campaign, over 40,000 exhaust plume points were identified using the macroscopic approach. The

  20. A chemical extraction method for mimicking bioavailability of polycyclic aromatic hydrocarbons to wheat grown in soils containing various amounts of organic matter

    SciTech Connect

    Shu Tao; Fuliu Xu; Wenxin Liu; Yanhong Cui; Raymond M. Coveney, Jr.

    2006-04-01

    Severe contamination of agricultural soils by polycyclic aromatic hydrocarbons (PAHs) occurs in many places in China mainly as a result of coal and biomass combustion. Because ingestion is the main source of human exposure to PAHs and vegetables are basic ingredients for the Chinese diet, it is important to know how and to what extent PAHs are accumulated in vegetables produced in contaminated soils. This study, evaluated the extent to which organic matter contents in soils influence the accumulation of PAHs by the roots of wheat plants and have developed a rapid chemical method for determining the bioavailability of PAH. Four PAHs, naphthalene, acenaphthylene, fluorene, and phenanthrene, were added to natural soil samples with different amounts of organic matter for pot experiments to evaluate apparent bioavailability of PAHs to wheat roots (Triticum aestivum L.). The extractabilities of PAHs in the soil were tested by a sequential extraction scheme using accelerated solvent extraction with water, n-hexane, and a mixture of dichloromethane and acetone as solvents. The water or n-hexane-extractable PAHs were positively correlated to dissolved organic matter (DOM) and negatively correlated to total organic matter (TOM), indicating mobilization and immobilization effects of DOM and TOM on soil PAHs, respectively. The apparent accumulation of PAHs by wheat roots was also positively and negatively correlated to DOM and TOM, respectively. As a result, there are positive correlations between the amounts of PAHs extracted by water or n-hexane and the quantities accumulated in plant roots, suggesting the feasibility of using water- or n-hexanes-extractable fractions as indicators of PAH availability to plants. 19 refs., 8 figs., 1 tab.

  1. Emulsification liquid-liquid microextraction based on deep eutectic solvent: An extraction method for the determination of benzene, toluene, ethylbenzene and seven polycyclic aromatic hydrocarbons from water samples.

    PubMed

    Khezeli, Tahere; Daneshfar, Ali; Sahraei, Reza

    2015-12-18

    In this study, for the first time, a simple, inexpensive and sensitive method named emulsification liquid-liquid microextraction based on deep eutectic solvent (ELLME-DES) was used for the extraction of benzene, toluene, ethylbenzene (BTE) and seven polycyclic aromatic hydrocarbons (PAHs) from water samples. In a typical experiment, 100μL of DES (as water-miscible extraction solvent) was added to 1.5mL of sample solution containing target analytes. A homogeneous solution was formed immediately. Injection of 100μL of THF (as emulsifier agent) into homogeneous solution provided a turbid state. After extraction, phase separation (aqueous phase/DES rich phase) was performed by centrifugation. DES rich phase was withdrawn by a micro-syringe and submitted to isocratic reverse-phase HPLC with UV detection. Under optimum conditions obtained by response surface methodology (RSM) and desirability function (DF), the calibration graphs were linear in the concentration range from 10 to 200μg/L for benzene, 10-400μg/L for toluene, 1-400μg/L for ethylbenzene, biphenyl, chrysene and fluorene, and 0.1-400μg/L for anthracene, benzo[a]pyrene, phenanthrene and pyrene. The coefficients of determination (r(2)) and limits of detection were 0.9924-0.9997 and 0.02-6.8μg/L, respectively. This procedure was successfully applied to the determination of target analytes in spiked water samples. The relative mean recoveries ranged from 93.1 to 103.3%.

  2. Emulsification liquid-liquid microextraction based on deep eutectic solvent: An extraction method for the determination of benzene, toluene, ethylbenzene and seven polycyclic aromatic hydrocarbons from water samples.

    PubMed

    Khezeli, Tahere; Daneshfar, Ali; Sahraei, Reza

    2015-12-18

    In this study, for the first time, a simple, inexpensive and sensitive method named emulsification liquid-liquid microextraction based on deep eutectic solvent (ELLME-DES) was used for the extraction of benzene, toluene, ethylbenzene (BTE) and seven polycyclic aromatic hydrocarbons (PAHs) from water samples. In a typical experiment, 100μL of DES (as water-miscible extraction solvent) was added to 1.5mL of sample solution containing target analytes. A homogeneous solution was formed immediately. Injection of 100μL of THF (as emulsifier agent) into homogeneous solution provided a turbid state. After extraction, phase separation (aqueous phase/DES rich phase) was performed by centrifugation. DES rich phase was withdrawn by a micro-syringe and submitted to isocratic reverse-phase HPLC with UV detection. Under optimum conditions obtained by response surface methodology (RSM) and desirability function (DF), the calibration graphs were linear in the concentration range from 10 to 200μg/L for benzene, 10-400μg/L for toluene, 1-400μg/L for ethylbenzene, biphenyl, chrysene and fluorene, and 0.1-400μg/L for anthracene, benzo[a]pyrene, phenanthrene and pyrene. The coefficients of determination (r(2)) and limits of detection were 0.9924-0.9997 and 0.02-6.8μg/L, respectively. This procedure was successfully applied to the determination of target analytes in spiked water samples. The relative mean recoveries ranged from 93.1 to 103.3%. PMID:26614169

  3. CORONA-INDUCED PHOTOXIDATION OF ALCOHOLS AND HYDROCARBONS OVER TIO2 IN THE ABSENCE OF A UV LIGHT SOURCE - A NOVEL AND ENVIRONMENTALLY FRIENDLY METHOD FOR OXIDATION

    EPA Science Inventory

    Corona-induced photooxidation is a novel oxidation methodology for the efficient oxidation of alcohols and hydrocarbons utilizing the advantage of both the high oxidizing power of ozone formed in the reactor as well as the photooxidation capability of the UV light generated durin...

  4. Recovering hydrocarbons from hydrocarbon-containing vapors

    DOEpatents

    Mirza, Zia I.; Knell, Everett W.; Winter, Bruce L.

    1980-09-30

    Values are recovered from a hydrocarbon-containing vapor by contacting the vapor with quench liquid consisting essentially of hydrocarbons to form a condensate and a vapor residue, the condensate and quench fluid forming a combined liquid stream. The combined liquid stream is mixed with a viscosity-lowering liquid to form a mixed liquid having a viscosity lower than the viscosity of the combined liquid stream to permit easy handling of the combined liquid stream. The quench liquid is a cooled portion of the mixed liquid. Viscosity-lowering liquid is separated from a portion of the mixed liquid and cycled to form additional mixed liquid.

  5. The novel combination of dynamic vapour sorption gravimetric analysis and near infra-red spectroscopy as a hyphenated technique.

    PubMed

    Lane, R A; Buckton, G

    2000-10-10

    The novel combination of an environmental controlled gas flow microbalance (Dynamic Vapour Sorption, Surface Measurement Systems, UK) with a NIR spectrometer (Foss NIR Systems) is described. The study follows the gravimetric changes and the spectroscopic changes in the amorphous and crystalline states of lactose at 298 K. NIR spectra and gravimetric water sorption were recorded simultaneously for the same sample. Differentiation of the amorphous and crystalline states of lactose was possible from the evaluation of peak intensity and shifts in the known fingerprint regions of the NIR spectra, i.e. 1350-1510 and 1825-1975 nm which correspond to water changes, and 2075-2160 nm which tends to illustrate changes in the organic/structural backbone character. Gravimetric analysis confirmed that the amorphous lactose crystallised, as weight changes can be linked to structural changes. The combined technique maintains the high performance of the DVS microbalance for gravimetric analysis but also provides a preset, regulated and controllable environment for studies using NIR spectroscopy probes, which was previously not possible. The results obtained agree with accepted data, and therefore provide validation for the hyphenation technique. The use of the combined DVS-NIR instrument has indicated two new pieces of information, firstly the amorphous form loses some water before the crystallisation is detectable. This indicates that water desorption may precede crystallisation, rather than the other way around, and secondly, the sample has completed crystallisation before water desorption has ended.

  6. Hydrocarbon Spectral Database

    National Institute of Standards and Technology Data Gateway

    SRD 115 Hydrocarbon Spectral Database (Web, free access)   All of the rotational spectral lines observed and reported in the open literature for 91 hydrocarbon molecules have been tabulated. The isotopic molecular species, assigned quantum numbers, observed frequency, estimated measurement uncertainty and reference are given for each transition reported.

  7. Method for inverting reflection trace data from 3-D and 4-D seismic surveys and identifying subsurface fluid and pathways in and among hydrocarbon reservoirs based on impedance models

    DOEpatents

    He, Wei; Anderson, Roger N.

    1998-01-01

    A method is disclosed for inverting 3-D seismic reflection data obtained from seismic surveys to derive impedance models for a subsurface region, and for inversion of multiple 3-D seismic surveys (i.e., 4-D seismic surveys) of the same subsurface volume, separated in time to allow for dynamic fluid migration, such that small scale structure and regions of fluid and dynamic fluid flow within the subsurface volume being studied can be identified. The method allows for the mapping and quantification of available hydrocarbons within a reservoir and is thus useful for hydrocarbon prospecting and reservoir management. An iterative seismic inversion scheme constrained by actual well log data which uses a time/depth dependent seismic source function is employed to derive impedance models from 3-D and 4-D seismic datasets. The impedance values can be region grown to better isolate the low impedance hydrocarbon bearing regions. Impedance data derived from multiple 3-D seismic surveys of the same volume can be compared to identify regions of dynamic evolution and bypassed pay. Effective Oil Saturation or net oil thickness can also be derived from the impedance data and used for quantitative assessment of prospective drilling targets and reservoir management.

  8. Method for inverting reflection trace data from 3-D and 4-D seismic surveys and identifying subsurface fluid and pathways in and among hydrocarbon reservoirs based on impedance models

    DOEpatents

    He, W.; Anderson, R.N.

    1998-08-25

    A method is disclosed for inverting 3-D seismic reflection data obtained from seismic surveys to derive impedance models for a subsurface region, and for inversion of multiple 3-D seismic surveys (i.e., 4-D seismic surveys) of the same subsurface volume, separated in time to allow for dynamic fluid migration, such that small scale structure and regions of fluid and dynamic fluid flow within the subsurface volume being studied can be identified. The method allows for the mapping and quantification of available hydrocarbons within a reservoir and is thus useful for hydrocarbon prospecting and reservoir management. An iterative seismic inversion scheme constrained by actual well log data which uses a time/depth dependent seismic source function is employed to derive impedance models from 3-D and 4-D seismic datasets. The impedance values can be region grown to better isolate the low impedance hydrocarbon bearing regions. Impedance data derived from multiple 3-D seismic surveys of the same volume can be compared to identify regions of dynamic evolution and bypassed pay. Effective Oil Saturation or net oil thickness can also be derived from the impedance data and used for quantitative assessment of prospective drilling targets and reservoir management. 20 figs.

  9. Photocatalyzed oxidation of hydrocarbons in zeolite cages

    SciTech Connect

    Frei, H.; Blatter, F.; Sun, H.

    1996-06-01

    Oxidation of hydrocarbons by molecular oxygen is a key process in chemical industry. But reactions that use O{sub 2} as the primary oxidant often produce large amounts of unwanted byproducts. One major reason that selectivities are low is that the desired products (such as alcohols or carbonyls) are more easily oxidized by O{sub 2} than the parent hydrocarbon. The authors recently discovered a simple method that gives partial oxidation of small alkenes, alkanes, and alkyl-substituted benzenes by O{sub 2} at unprecedented selectivity, even at high conversion of the hydrocarbon. The approach is based on visible light-induced chemistry of hydrocarbon-O{sub 2} collisional pairs in the cages of large-pore zeolites. Reactions are conducted at ambient temperature in the absence of solvent or photosensitizer. Here the authors describe the most interesting reactions established thus far and define issues that pertain to scale-up of the method.

  10. NIST gravimetrically prepared atmospheric level methane in dry air standards suite.

    PubMed

    Rhoderick, George C; Carney, Jennifer; Guenther, Franklin R

    2012-04-17

    The Gas Metrology Group at the National Institute of Standards and Technology was tasked, by a congressional climate change act, to support the atmospheric measurement community through standards development of key greenhouse gases. This paper discusses the development of a methane (CH(4)) primary standard gas mixture (PSM) suite to support CH(4) measurement needs over a large amount-of-substance fraction range 0.3-20,000 μmol mol(-1), but with emphasis at the atmospheric level 300-4000 nmol mol(-1). Thirty-six CH(4) in dry air PSMs were prepared in 5.9 L high-pressure aluminum cylinders with use of a time-tested gravimetric technique. Ultimately 14 of these 36 PSMs define a CH(4) standard suite covering the nominal ambient atmospheric range of 300-4000 nmol mol(-1). Starting materials of pure CH(4) and cylinders of dry air were exhaustively analyzed to determine the purity and air composition. Gas chromatography with flame-ionization detection (GC-FID) was used to determine a CH(4) response for each of the 14 PSMs where the reproducibility of average measurement ratios as a standard error was typically (0.04-0.26) %. An ISO 6134-compliant generalized least-squares regression (GenLine) program was used to analyze the consistency of the CH(4) suite. All 14 PSMs passed the u-test with residuals between the gravimetric and the GenLine solution values being between -0.74 and 1.31 nmol mol(-1); (0.00-0.16)% relative absolute. One of the 14 PSMs, FF4288 at 1836.16 ± 0.75 nmol mol(-1) (k = 1) amount-of-substance fraction, was sent to the Korea Research Institute of Standards and Science (KRISS), the Republic of Korea's National Metrology Institute, for comparison. The same PSM was subsequently sent to the National Oceanic and Atmospheric Administration (NOAA) for analysis to their standards. Results show agreement between KRISS-NIST of +0.13% relative (+2.3 nmol mol(-1)) and NOAA-NIST of -0.14% relative (-2.54 nmol mol(-1)).

  11. Plasma-assisted conversion of solid hydrocarbon to diamond

    DOEpatents

    Valone, Steven M.; Pattillo, Stevan G.; Trkula, Mitchell; Coates, Don M.; Shah, S. Ismat

    1996-01-01

    A process of preparing diamond, e.g., diamond fiber, by subjecting a hydrocarbon material, e.g., a hydrocarbon fiber, to a plasma treatment in a gaseous feedstream for a sufficient period of time to form diamond, e.g., a diamond fiber is disclosed. The method generally further involves pretreating the hydrocarbon material prior to treatment with the plasma by heating within an oxygen-containing atmosphere at temperatures sufficient to increase crosslinking within said hydrocarbon material, but at temperatures insufficient to melt or decompose said hydrocarbon material, followed by heating at temperatures sufficient to promote outgassing of said crosslinked hydrocarbon material, but at temperatures insufficient to convert said hydrocarbon material to carbon.

  12. Hydrocarbon Rocket Technology Impact Forecasting

    NASA Technical Reports Server (NTRS)

    Stuber, Eric; Prasadh, Nishant; Edwards, Stephen; Mavris, Dimitri N.

    2012-01-01

    Ever since the Apollo program ended, the development of launch propulsion systems in the US has fallen drastically, with only two new booster engine developments, the SSME and the RS-68, occurring in the past few decades.1 In recent years, however, there has been an increased interest in pursuing more effective launch propulsion technologies in the U.S., exemplified by the NASA Office of the Chief Technologist s inclusion of Launch Propulsion Systems as the first technological area in the Space Technology Roadmaps2. One area of particular interest to both government agencies and commercial entities has been the development of hydrocarbon engines; NASA and the Air Force Research Lab3 have expressed interest in the use of hydrocarbon fuels for their respective SLS Booster and Reusable Booster System concepts, and two major commercially-developed launch vehicles SpaceX s Falcon 9 and Orbital Sciences Antares feature engines that use RP-1 kerosene fuel. Compared to engines powered by liquid hydrogen, hydrocarbon-fueled engines have a greater propellant density (usually resulting in a lighter overall engine), produce greater propulsive force, possess easier fuel handling and loading, and for reusable vehicle concepts can provide a shorter turnaround time between launches. These benefits suggest that a hydrocarbon-fueled launch vehicle would allow for a cheap and frequent means of access to space.1 However, the time and money required for the development of a new engine still presents a major challenge. Long and costly design, development, testing and evaluation (DDT&E) programs underscore the importance of identifying critical technologies and prioritizing investment efforts. Trade studies must be performed on engine concepts examining the affordability, operability, and reliability of each concept, and quantifying the impacts of proposed technologies. These studies can be performed through use of the Technology Impact Forecasting (TIF) method. The Technology Impact

  13. Emulsification of hydrocarbons by subsurface bacteria

    USGS Publications Warehouse

    Francy, D.S.; Thomas, J.M.; Raymond, R.L.; Ward, C.H.

    1991-01-01

    Biosurfactants have potential for use in enhancement of in situ biorestoration by increasing the bioavailability of contaminants. Microorganisms isolated from biostimulated, contaminated and uncontaminated zones at the site of an aviation fuel spill and hydrocarbon-degrading microorganisms isolated from sites contaminated with unleaded gasoline were examined for their abilities to emulsify petroleum hydrocarbons. Emulsifying ability was quantified by a method involving agitation and visual inspection. Biostimulated-zone microbes and hydrocarbon-degrading microorganisms were the best emulsifiers as compared to contaminated and uncontaminated zone microbes. Biostimulation (nutrient and oxygen addition) may have been the dominant factor which selected for and encouraged growth of emulsifiers; exposure to hydrocarbon was also important. Biostimulated microorganisms were better emulsifiers of aviation fuel (the contaminant hydrocarbon) than of heavier hydrocarbon to which they were not previously exposed. By measuring surface tension changes of culture broths, 11 out of 41 emulsifiers tested were identified as possible biosurfactant producers and two isolates produced large surface tension reductions indicating the high probability of biosurfactant production.Biosurfactants have potential for use in enhancement of in situ biorestoration by increasing the bioavailability of contaminants. Microorganisms isolated from biostimulated, contaminated and uncontaminated zones at the site of an aviation fuel spill and hydrocarbon-degrading microorganisms isolated from sites contaminated with unleaded gasoline were examined for their abilities to emulsify petroleum hydrocarbons. Emulsifying ability was quantified by a method involving agitation and visual inspection. Biostimulated-zone microbes and hydrocarbon-degrading microorganisms were the best emulsifiers as compared to contaminated and uncontaminated zone microbes. Biostimulation (nutrient and oxygen addition) may have been

  14. Combining gravimetric and vibrational spectroscopy measurements to quantify first- and second-shell hydration layers in polyimides with different molecular architectures.

    PubMed

    Musto, Pellegrino; Mensitieri, Giuseppe; Lavorgna, Marino; Scarinzi, Gennaro; Scherillo, Giuseppe

    2012-02-01

    In-situ Fourier transform infrared (FTIR) measurements have been carried out at different relative pressures of water vapor to study the H(2)O diffusion in three polyimides differing in their molecular structure and fluorine substitution. Spectral data have been analyzed by difference spectroscopy, least-squares curve fitting, and two-dimensional (2D) correlation spectroscopy, which provided molecular level information on the diffusion mechanism. In particular, two distinct water species were identified corresponding, respectively, to the first and second-shell hydration layers. The spectroscopic analysis demonstrated that the relative population of these species is a function of the total water content in the system. A method has been devised to quantify the water concentration in the two hydration layers, based on a combination of spectroscopic and gravimetric data. The results have been compared with those from an earlier spectroscopic approach reported in the literature and based on the analysis of the carbonyl region.

  15. The determination of equilibrium constants, DeltaG, DeltaH and DeltaS for vapour interaction with a pharmaceutical drug, using gravimetric vapour sorption.

    PubMed

    Willson, Richard J; Beezer, Anthony E

    2003-06-01

    The application of gravimetric vapour sorption (GVS) to the characterisation of pharmaceutical drugs is often restricted to the study of gross behaviour such as a measure of hygroscopicity. Although useful in early development of a drug substance, for example, in salt selection screening exercises, such types of analysis may not contribute to a fundamental understanding of the properties of the material. This paper reports a new methodology for GVS experimentation that will allow specific sorption parameters to be calculated; equilibrium constant (K), van't Hoff enthalpy change (DeltaH(v)), Gibbs free energy for sorption (DeltaG) and the entropy change for sorption (DeltaS). Unlike other reports of such type of analysis that require the application of a specific model, this method is model free. The analysis does require that over the narrow temperature range of the study DeltaH(v) is constant and there is no change in interaction mechanism.

  16. Determination of the parameters of binding between lipopolysaccharide and chitosan and its N-acetylated derivative using a gravimetric piezoquartz biosensor.

    PubMed

    Naberezhnykh, G A; Gorbach, V I; Kalmykova, E N; Solov'eva, T F

    2015-03-01

    The interaction of endotoxin (lipopolysaccharide - LPS) with low molecular weight chitosan (5.5 kDa), its N-acylated derivative and chitoliposomes was studied using a gravimetric piezoelectric quartz crystal microbalance biosensor. The optimal conditions for the formation of a biolayer based on immobilized LPS on the resonator surface and its regeneration were elaborated. The association and dissociation rate constants for LPS binding to chitosans were determined and the affinity constants (Kaf) were calculated based on the data on changes in the oscillation frequency of the quartz crystal resonator. The Kaf values correlated with the ones obtained using other methods. The affinity of N-acylated chitosan binding to LPS was higher than that of the parent chitosan binding to LPS. Based on the results obtained, we suggest that water-soluble N-acylated derivatives of chitosan with low degree of substitution of amino groups could be useful compounds for endotoxin binding and neutralization. PMID:25637889

  17. An instrument for gravimetric calibration of flow devices with corrosive gases

    SciTech Connect

    Remenyik, C.J.; Hylton, J.O.

    1995-04-01

    An instrument was developed for the calibration of mass flow controllers primarily used in the production of semiconductor wafers. Almost all other types of such calibrators require measurement of temperature, pressure and volume. This instrument measures the weight of gas collected in a container and makes measuring those thermodynamic variables unnecessary. The need to measure the weight of the gas container is eliminated by submerging it in a liquid (presently water) and balancing its weight with the force of buoyancy. The accuracy of this Gravimetric Calibrator is unaffected by the pressure and temperature of the gas. The Calibrator can also measure reactive, corrosive, and non-ideal gases. The container remains connected to the process by a torsion capillary, and a load cell measures the changing gas weight continuously throughout the measuring process. A prototype was designed for gas flows ranging from 1 sccm of hydrogen to 10,000 sccm of tungsten hexafluoride, constructed, tested, and used to calibrate flow devices. Experience with the prototype and results are presented, and plans for further developments are discussed. Design of a version for the flow range from 0.1 sccm to 100 sccm is in progress.

  18. Joint Interpretation of Magnetotelluric and Gravimetric Data from the South American Paraná Basin

    NASA Astrophysics Data System (ADS)

    Santos, E. B.; Santos, H. B.; Vitorello, I.; Pádua, M. B.

    2013-05-01

    The Paraná Basin is a large sedimentary basin in central-eastern South America that extends through Brazil, Paraguay, Uruguay and Argentina. Evolved completely over the South American continental crust, this Paleozoic basin is filled with sedimentary and volcanic rocks deposited from the Silurian to the Cretaceous, when a significant basaltic effusion covered almost the entire area of the basin. A series of superposed sedimentary and volcanic rock layers were laid down under the influence of different tectonic settings, probably originated from distant collisional dynamics of continental boards that led to the amalgamation of Gondwanaland. The current boundaries of the basin can be the result of issuing erosional or of tectonic origin, such as the building up of large arches and faults. To evaluate the deep structural architecture of the lithosphere under a sedimentary basin is a great challenge, requiring the integration of different geophysical and geological studies. In this paper, we present the resulting Paraná Basin lithospheric model, obtained from processing and inversion of broadband and long-period magnetotelluric soundings along an E-W profile across the central part of the basin, complemented by a qualitative joint interpretation of gravimetric data, in order to obtain a more precise geoelectric model of the deep structure of the region.

  19. Gravimetric analysis and differential scanning calorimetric studies on glycerin-induced skin hydration.

    PubMed

    Lee, Ae-Ri Cho; Moon, Hee Kyung

    2007-11-01

    A thermal gravimetric analysis (TGA) and a differential scanning calorimetry (DSC) were carried out to characterize the water property and an alteration of lipid phase transition of stratum corneum (SC) by glycerin. In addition, the relationship between steady state skin permeation rate and skin hydration in various concentrations of glycerin was investigated. Water vapor absorption-desorption was studied in the hairless mouse stratum corneum. Dry SC samples were exposed to different conc. of glycerin (0-50%) followed by exposure to dry air and the change in weight property was monitored over time by use of TGA. In DSC study, significant decrease in DeltaH of the lipid transition in 10% glycerin and water treated sample: the heat of lipid transition of normal, water, 10% glycerin treated SC were 6.058, 4.412 and 4.316 mJ/mg, respectively. In 10% glycerin treated SCs, the Tc of water shifts around 129 degrees C, corresponding to the weakly bound secondary water. In 40% glycerin treated SC, the Tc of water shifts to 144 degrees C corresponding to strongly bound primary water. There was a good correlation between the hydration property of the skin and the steady state skin flux with the correlation coefficient (r2=0.94). As the hydration increased, the steady state flux increased. As glycerin concentration increased, hydration property decreased. High diffusivity induced by the hydration effect of glycerin and water could be the major contributing factor for the enhanced skin permeation of nicotinic acid (NA).

  20. Evaluation of kinetic parameters for water soluble crystals by thermo gravimetric analysis

    NASA Astrophysics Data System (ADS)

    Rama, S.; Surendra Dilip, C.; Perumal, Rajesh Narayana

    2015-01-01

    This work elevates the relevance of kinetic parameters of nucleation and thermal decomposition for water soluble crystals. The positive soluble Potassium Dihydrogen Phosphate (KDP) and negative soluble Lithium Sulfate Monohydrate (LSMH) materials were chosen for the kinetic evaluation. The results obtained from the classical nucleation theory are verified with the kinetic parameters which are evaluated from thermo gravimetric analysis. Nucleation parameters of a crystallization process such as interfacial energy (σ), volume free energy (ΔGv), critical energy barrier for nucleation (ΔG*), radius of the critical nucleus (r*) and nucleation rate (J) of the positive (KDP) and negative solubility (LSMH) crystals are determined from the classical nucleation theory of solubility-enthalpy relation. The kinetic parameters viz. the order of reaction, enthalpy, Gibbs free energy of activation, frequency factor, and entropy of activation are obtained from the TG based models viz. Horowitz-Metzger, Coats-Redfern and Piloyan-Novikova. The effect of varying temperature with relative variation on Gibbs free energy for both positive and negative solubility crystals is also discussed. The developed model holds good for both positive and negative solubility crystals.

  1. Automated Gravimetric Calibration to Optimize the Accuracy and Precision of TECAN Freedom EVO Liquid Handler.

    PubMed

    Bessemans, Laurent; Jully, Vanessa; de Raikem, Caroline; Albanese, Mathieu; Moniotte, Nicolas; Silversmet, Pascal; Lemoine, Dominique

    2016-10-01

    High-throughput screening technologies are increasingly integrated into the formulation development process of biopharmaceuticals. The performance of liquid handling systems is dependent on the ability to deliver accurate and precise volumes of specific reagents to ensure process quality. We have developed an automated gravimetric calibration procedure to adjust the accuracy and evaluate the precision of the TECAN Freedom EVO liquid handling system. Volumes from 3 to 900 µL using calibrated syringes and fixed tips were evaluated with various solutions, including aluminum hydroxide and phosphate adjuvants, β-casein, sucrose, sodium chloride, and phosphate-buffered saline. The methodology to set up liquid class pipetting parameters for each solution was to split the process in three steps: (1) screening of predefined liquid class, including different pipetting parameters; (2) adjustment of accuracy parameters based on a calibration curve; and (3) confirmation of the adjustment. The run of appropriate pipetting scripts, data acquisition, and reports until the creation of a new liquid class in EVOware was fully automated. The calibration and confirmation of the robotic system was simple, efficient, and precise and could accelerate data acquisition for a wide range of biopharmaceutical applications. PMID:26905719

  2. Automated Gravimetric Calibration to Optimize the Accuracy and Precision of TECAN Freedom EVO Liquid Handler

    PubMed Central

    Bessemans, Laurent; Jully, Vanessa; de Raikem, Caroline; Albanese, Mathieu; Moniotte, Nicolas; Silversmet, Pascal; Lemoine, Dominique

    2016-01-01

    High-throughput screening technologies are increasingly integrated into the formulation development process of biopharmaceuticals. The performance of liquid handling systems is dependent on the ability to deliver accurate and precise volumes of specific reagents to ensure process quality. We have developed an automated gravimetric calibration procedure to adjust the accuracy and evaluate the precision of the TECAN Freedom EVO liquid handling system. Volumes from 3 to 900 µL using calibrated syringes and fixed tips were evaluated with various solutions, including aluminum hydroxide and phosphate adjuvants, β-casein, sucrose, sodium chloride, and phosphate-buffered saline. The methodology to set up liquid class pipetting parameters for each solution was to split the process in three steps: (1) screening of predefined liquid class, including different pipetting parameters; (2) adjustment of accuracy parameters based on a calibration curve; and (3) confirmation of the adjustment. The run of appropriate pipetting scripts, data acquisition, and reports until the creation of a new liquid class in EVOware was fully automated. The calibration and confirmation of the robotic system was simple, efficient, and precise and could accelerate data acquisition for a wide range of biopharmaceutical applications. PMID:26905719

  3. An Instrument for Gravimetric Calibration of Flow Devices with Corrosive Gases

    SciTech Connect

    Hylton, J.O.; Remenyik, C.J.

    1999-06-27

    An instrument was developed for the direct mass flow calibration of gas flowmeters that does not require measurement of temperature, pressure, or specific volume. This instrument measures the weight of gas collected in a container and makes measuring those thermodynamic variables unnecessary. The need to measure the weight of the gas container is eliminated by submerging it in a liquid (presently water) and balancing its weight with the force of buoyancy. The accuracy of this Gravimetric Calibrator is unaffected by the pressure and temperature of the gas. The Calibrator can also measure reactive, corrosive, and non-ideal gases. The container remains connected to the process by a torsion capillary, and a load cell measures the changing gas weight continuously throughout the measuring process. A prototype was designed for gas flows ranging from 1 sccm of hydrogen to 10,000 sccm of tungsten hexafluoride, constructed, tested, and used to calibrate flow devices. Experience with the prototype and results are presented, and plans for further developments are discussed.

  4. Polyaniline nanofiber sponge filled graphene foam as high gravimetric and volumetric capacitance electrode

    NASA Astrophysics Data System (ADS)

    Pedrós, J.; Boscá, A.; Martínez, J.; Ruiz-Gómez, S.; Pérez, L.; Barranco, V.; Calle, F.

    2016-06-01

    A 3D hierarchical porous composite structure is developed via the controlled electrodeposition of a polyaniline nanofiber sponge (PANI-NFS) that fills the pores of a chemical vapor deposited graphene foam (GF). The PANI-NFS/GF composite combines the efficient electronic transport in the GF scaffold (with 100-500 μm pore size) with the rapid diffusion of the electrolyte ions into the high-specific-surface-area and densely-packed PANI-NFS (with 100-500 nm pore size). The factor of 1000 in the pore hierarchy and the synergy between the materials, that form a supercapacitor composite electrode with an integrated extended current collector, lead to both very high gravimetric and volumetric capacitances. In particular, values of 1474 F g-1 and 86 F cm-3 for a GF filling factor of 11% (leading to an estimated value of 782 F cm-3 for 100%), respectively, are obtained at a current density of 0.47 A g-1. Moreover, the composite electrode presents a capacitance retention of 83% after 15000 cycles. This excellent behavior makes the PANI-NFS/GF composite electrodes very attractive for high-performance supercapacitors.

  5. Integration of remotely-sensed geobotanical and structural methods for hydrocarbon exploration in West-Central West Virginia. Quartery report, May 1, 1996--July 31, 1996

    SciTech Connect

    1997-06-01

    Progress is reported on hydrocarbon exploration in West-Central West Virginia. In this period, the following tasks were carried out: a reconnaissance soil gas geochemical survey was performed at the Volcano test site and at the Lewis County test site; a geobotanical analysis of the September imagery was carried out in order to highlight spectral anomalies that appear to be associated with the historic volcano field and the Lewis County test site; and multi-temporal spectral reflectance measurements continued.

  6. Plasma Processing Of Hydrocarbon

    SciTech Connect

    Grandy, Jon D; Peter C. Kong; Brent A. Detering; Larry D. Zuck

    2007-05-01

    The Idaho National Laboratory (INL) developed several patented plasma technologies for hydrocarbon processing. The INL patents include nonthermal and thermal plasma technologies for direct natural gas to liquid conversion, upgrading low value heavy oil to synthetic light crude, and to convert refinery bottom heavy streams directly to transportation fuel products. Proof of concepts has been demonstrated with bench scale plasma processes and systems to convert heavy and light hydrocarbons to higher market value products. This paper provides an overview of three selected INL patented plasma technologies for hydrocarbon conversion or upgrade.

  7. Total organic carbon and gas chromatography-mass spectroscopy methods to determine total carbon and hydrocarbons in mercuric iodide single crystals

    NASA Astrophysics Data System (ADS)

    Steinberg, S.; Kaplan, I.; Schieber, M.; Ortale, C.; Skinner, N.; van den Berg, L.

    1989-11-01

    Total organic carbon was determined by measuring the CO2 produced by combustion in a sealed quartz vessel. The CO2 was quantified by nondispersive IR and by titration using commercial detectors. The total organic carbon was found to be around 10-100 μg/g in both starting materials and in single crystals. Gas chromatography-mass spectroscopy (GC/MS) measurements were made on hexane extracts of mercuric iodide (HgI2) dissolved in potassium iodide solution. Hydrocarbons starting with C10 (DIENE) and up to C26 were found. In addition, phthalates, such as diethyl and dioctyl phthalate were also found. Some of the organic compounds, for example, such hydrocarbons as branched nC16, nC20, nC21, nC22, nC23, and nC24, were present in some HgI2 materials in quantities of the order of weight ppm, but were eliminated in the purification process and were not found in the single crystals. Other organic compounds such as the phthalates were not always eliminated and were identified in the single crystals. In general, the GC/MS could identify only hydrocarbons of C10 and higher which account for only a few percent of the total organic carbon determined by oxidation.

  8. Determination of descriptors for polycyclic aromatic hydrocarbons and related compounds by chromatographic methods and liquid-liquid partition in totally organic biphasic systems.

    PubMed

    Ariyasena, Thiloka C; Poole, Colin F

    2014-09-26

    Retention factors on several columns and at various temperatures using gas chromatography and from reversed-phase liquid chromatography on a SunFire C18 column with various mobile phase compositions containing acetonitrile, methanol and tetrahydrofuran as strength adjusting solvents are combined with liquid-liquid partition coefficients in totally organic biphasic systems to calculate descriptors for 23 polycyclic aromatic hydrocarbons and eighteen related compounds of environmental interest. The use of a consistent protocol for the above measurements provides descriptors that are more self consistent for the estimation of physicochemical properties (octanol-water, air-octanol, air-water, aqueous solubility, and subcooled liquid vapor pressure). The descriptor in this report tend to have smaller values for the L and E descriptors and random differences in the B and S descriptors compared with literature sources. A simple atom fragment constant model is proposed for the estimation of descriptors from structure for polycyclic aromatic hydrocarbons. The new descriptors show no bias in the prediction of the air-water partition coefficient for polycyclic aromatic hydrocarbons unlike the literature values.

  9. Hydrocarbon and nonhydrocarbon derivatives of cyclopropane

    NASA Technical Reports Server (NTRS)

    Slabey, Vernon A; Wise, Paul H; Gibbons, Louis C

    1953-01-01

    The methods used to prepare and purify 19 hydrocarbon derivatives of cyclopropane are discussed. Of these hydrocarbons, 13 were synthesized for the first time. In addition to the hydrocarbons, six cyclopropylcarbinols, five alkyl cyclopropyl ketones, three cyclopropyl chlorides, and one cyclopropanedicarboxylate were prepared as synthesis intermediates. The melting points, boiling points, refractive indices, densities, and, in some instances, heats of combustion of both the hydrocarbon and nonhydrocarbon derivatives of cyclopropane were determined. These data and the infrared spectrum of each of the 34 cyclopropane compounds are presented in this report. The infrared absorption bands characteristic of the cyclopropyl ring are discussed, and some observations are made on the contribution of the cyclopropyl ring to the molecular refractions of cyclopropane compounds.

  10. To what extent can aerosol water explain the discrepancy between model calculated and gravimetric PM10 and PM2.5?

    NASA Astrophysics Data System (ADS)

    Tsyro, S. G.

    2004-09-01

    Inter-comparisons of European air quality models show that regional transport models, including the EMEP (Co-operative Programme for monitoring and evaluation of the long-range transmission of air pollutants in Europe) aerosol model, tend to underestimate the observed concentrations of PM10 and PM2.5. Obviously, an accurate representation of the individual aerosol constituents is a prerequisite for adequate calculation of PM concentrations. On the other hand, available measurements on the chemical characterization of ambient particles reveal that full chemical PM mass closure is rarely achieved. The fraction unaccounted for by chemical analysis can comprise as much as 30-40% of gravimetric PM10 or PM2.5 mass. The unaccounted PM mass can partly be due to non-C atoms in organic aerosols and/or due to sampling and measurement artefacts. Moreover, a part of the unaccounted PM mass is likely to consist of water associated with particles. Thus, the gravimetrically measured particle mass does not necessarily represent dry PM10 and PM2.5 mass. This is thought to be one of the reasons for models under-prediction of observed PM, if calculated dry PM10 and PM2.5 concentrations are compared with measurements. The EMEP aerosol model has been used to study to what extent particle-bound water can explain the chemically unidentified PM mass in filter-based particle samples. Water content of PM2.5 and PM10 has been estimated with the model for temperature 20°C and relative humidity 50%, which are conditions required for equilibration of dust-loaded filters according to the Reference method recommended by the European Committee for Standardization (CEN). Model calculations for Europe show that, depending on particle composition, particle-bound water constitutes 20-35% of the annual mean PM10 and PM2.5 concentrations, which is consistent with existing experimental estimates. At two Austrian sites, in Vienna and Streithofen, where daily measurements of PM2.5 mass and chemical

  11. To what extent can aerosol water explain the discrepancy between model calculated and gravimetric PM10 and PM2.5?

    NASA Astrophysics Data System (ADS)

    Tsyro, S. G.

    2005-02-01

    Inter-comparisons of European air quality models show that regional transport models, including the EMEP (Co-operative Programme for monitoring and evaluation of the long-range transmission of air pollutants in Europe) aerosol model, tend to underestimate the observed concentrations of PM10 and PM2.5. Obviously, an accurate representation of the individual aerosol constituents is a prerequisite for adequate calculation of PM concentrations. On the other hand, available measurements on the chemical characterization of ambient particles reveal that full chemical PM mass closure is rarely achieved. The fraction unaccounted for by chemical analysis can comprise as much as 30-40% of gravimetric PM10 or PM2.5 mass. The unaccounted PM mass can partly be due to non-C atoms in organic aerosols and/or due to sampling and measurement artefacts. Moreover, a part of the unaccounted PM mass is likely to consist of water associated with particles. Thus, the gravimetrically measured particle mass does not necessarily represent dry PM10 and PM2.5 mass. This is thought to be one of the reasons for models under-prediction of observed PM, if calculated dry PM10 and PM2.5 concentrations are compared with measurements. The EMEP aerosol model has been used to study to what extent particle-bound water can explain the chemically unidentified PM mass in filter-based particle samples. Water content of PM2.5 and PM10 has been estimated with the model for temperature 20°C and relative humidity 50%, which are conditions required for equilibration of dust-loaded filters according to the Reference method recommended by the European Committee for Standardization (CEN). Model calculations for Europe show that, depending on particle composition, particle-bound water constitutes 20-35% of the annual mean PM10 and PM2.5 concentrations, which is consistent with existing experimental estimates. At two Austrian sites, in Vienna and Streithofen, where daily measurements of PM2.5 mass and chemical

  12. Membrane separation of hydrocarbons

    DOEpatents

    Funk, Edward W.; Kulkarni, Sudhir S.; Chang, Y. Alice

    1986-01-01

    Mixtures of heavy oils and light hydrocarbons may be separated by passing the mixture over a polymeric membrane which comprises a polymer capable of maintaining its integrity in the presence of hydrocarbon compounds at temperature ranging from about ambient to about 100.degree. C. and pressures ranging from about 50 to about 1000 psi. The membranes which possess pore sizes ranging from about 10 to about 500 Angstroms are cast from a solvent solution and recovered.

  13. Hydrocarbon geoscience research strategy

    SciTech Connect

    Not Available

    1990-04-01

    This document outlines a strategy for oil and gas related research focused on optimizing the economic producibility of the Nation's resources. The Hydrocarbon Geoscience Strategy was developed by the Hydrocarbon Geoscience Research Coordinating Committee of the Department of Energy (DOE). This strategy forms the basis for the development of DOE Fossil Energy's Oil Research Program Implementation Plan and Natural Gas Program Implementation Plan. 24 refs., 5 figs., 3 tabs.

  14. The spherical terrain correction and its effect on the gravimetric-isostatic Moho determination

    NASA Astrophysics Data System (ADS)

    Abrehdary, M.; Sjöberg, L. E.; Bagherbandi, M.

    2016-01-01

    In this study, the Moho depth is estimated based on the refined spherical Bouguer gravity disturbance and DTM2006 topographic data using the Vening Meinesz-Moritz gravimetric-isostatic hypothesis. In this context, we compute the refined spherical Bouguer gravity disturbances in a set of 1° × 1° blocks. The spherical terrain correction, a residual correction to each Bouguer shell, is computed using rock heights and ice sheet thicknesses from the DTM2006 and Earth2014 models. The study illustrates that the defined simple Bouguer gravity disturbance corrected for the density variations of the oceans, ice sheets and sediment basins and also the non-isostatic effects needs a significant terrain correction to become the refined Bouguer gravity disturbance, and that the isostatic gravity disturbance is significantly better defined by the latter disturbance plus a compensation attraction. Our study shows that despite the fact that the lateral variation of the crustal depth is rather smooth, the terrain affects the result most significantly in many areas. The global numerical results show that the estimated Moho depths by the simple and refined spherical Bouguer gravity disturbances and the seismic CRUST1.0 model agree to 5.6 and 2.7 km in RMS, respectively. Also, the mean value differences are 1.7 and 0.2 km, respectively. Two regional numerical studies show that the RMS differences between the Moho depths estimated based on the simple and refined spherical Bouguer gravity disturbance and that using CRUST1.0 model yield fits of 4.9 and 3.2 km in South America and yield 3.2 and 3.4 km in Fennoscandia, respectively.

  15. GRAVIMETRIC STUDY OF THE IXTLAN DE LOS HERVORES, GEOTHERMAL AREA, MIDWESTERN MEXICAN VOLCANIC BELT (MVB)

    NASA Astrophysics Data System (ADS)

    Gonzalez, T.; Ortiz, I.

    2009-12-01

    Analysis and interpretation of gravimetric anomalies over the Occidental-Central Mexican Volcanic Belt, sheds new light on the subsurface structure of the Ixtlan de los Hervores, geothermal area. In Mexico, there are several geothermal areas that have been exploited commercially (Cerro Prieto, Los Azufres, Los Humeros, Tres Virgenes fields). However, there are many other known fields that have not been exploited. This is the case in the area of "Ixtlan de los Hervores" in the state of Michoacan. The analyzed region covers a rectangular area, aproximality from 20o N to 20.5° N and 102° W to 102.2°W. In the region there are thick basalt flows. The area is characterized by low and elongated hills formed by volcanic flows and on a smaller scale lacustrian sediments and major normal faults with a NW-SE direction particularly, the Ixtlan-Encinal fault which controls the trace of the Duero River and the Pajacuarán fault. The anomaly map was compared with the surface geology and the anomalies were correlated with major volcanic features, since our main interest was in mapping the subsurface faults and volcanic bodies. Two profiles were selected that cross major anomalies and the geothermal zone of Ixtlan. The Talwani algorithm for 2-D polygonal bodies has been used for calculating the theoretical anomalies. The proposed models adequately explain the main observed geological features. The models are made up of two lithostratigraphic units of volcanic rocks, represented by the Tertiary basalts, which adequately reflect the area's volcanic environment. These basaltic units, corresponding to different volcanic events were cut by the Ixtlan well. Both models reflect the existence of the Ixtlan-Encinal fault, the most important feature in the area which is also responsible for the existence of the geothermal area.

  16. An NMR relaxometry and gravimetric study of gelatin-free aqueous polyacrylamide dosimeters

    NASA Astrophysics Data System (ADS)

    Babic, Steven; Schreiner, L. John

    2006-09-01

    In conformal radiation therapy, a high dose of radiation is given to a target volume to increase the probability of cure, and care is taken to minimize the dose to surrounding healthy tissue. The techniques used to achieve this are very complicated and the precise verification of the resulting three-dimensional (3D) dose distribution is required. Polyacrylamide gelatin (PAG) dosimeters with magnetic resonance imaging and optical computed tomography scanning provide the required 3D dosimetry with high spatial resolution. Many basic studies have characterized these chemical dosimeters that polymerize under irradiation. However, the investigation of the fundamental properties of the radiation-induced polymerization in PAG dosimeters is complicated by the presence of the background gelatin matrix. In this work, a gelatin-free model system for the study of the basic radiation-induced polymerization in PAG dosimeters has been developed. Experiments were performed on gelatin-free dosimeters, named aqueous polyacrylamide (APA) dosimeters, containing equal amounts of acrylamide and N,N'-methylene-bisacrylamide. The APA dosimeters were prepared with four different total monomer concentrations (2, 4, 6 and 8% by weight). Nuclear magnetic resonance (NMR) spin-spin and spin-lattice proton relaxation measurements at 20 MHz, and gravimetric analyses performed on all four dosimeters, show a continuous degree of polymerization over the dose range of 0-25 Gy. The developed NMR model explains the relationship observed between the relaxation data and the amount of crosslinked polymer formed at each dose. This model can be extended with gelatin relaxation data to provide a fundamental understanding of radiation-induced polymerization in the conventional PAG dosimeters.

  17. An NMR relaxometry and gravimetric study of gelatin-free aqueous polyacrylamide dosimeters.

    PubMed

    Babic, Steven; Schreiner, L John

    2006-09-01

    In conformal radiation therapy, a high dose of radiation is given to a target volume to increase the probability of cure, and care is taken to minimize the dose to surrounding healthy tissue. The techniques used to achieve this are very complicated and the precise verification of the resulting three-dimensional (3D) dose distribution is required. Polyacrylamide gelatin (PAG) dosimeters with magnetic resonance imaging and optical computed tomography scanning provide the required 3D dosimetry with high spatial resolution. Many basic studies have characterized these chemical dosimeters that polymerize under irradiation. However, the investigation of the fundamental properties of the radiation-induced polymerization in PAG dosimeters is complicated by the presence of the background gelatin matrix. In this work, a gelatin-free model system for the study of the basic radiation-induced polymerization in PAG dosimeters has been developed. Experiments were performed on gelatin-free dosimeters, named aqueous polyacrylamide (APA) dosimeters, containing equal amounts of acrylamide and N,N'-methylene-bisacrylamide. The APA dosimeters were prepared with four different total monomer concentrations (2, 4, 6 and 8% by weight). Nuclear magnetic resonance (NMR) spin-spin and spin-lattice proton relaxation measurements at 20 MHz, and gravimetric analyses performed on all four dosimeters, show a continuous degree of polymerization over the dose range of 0-25 Gy. The developed NMR model explains the relationship observed between the relaxation data and the amount of crosslinked polymer formed at each dose. This model can be extended with gelatin relaxation data to provide a fundamental understanding of radiation-induced polymerization in the conventional PAG dosimeters. PMID:16912375

  18. Mixture including hydrogen and hydrocarbon having pressure-temperature stability

    NASA Technical Reports Server (NTRS)

    Mao, Wendy L. (Inventor); Mao, Ho-Kwang (Inventor)

    2009-01-01

    The invention relates to a method of storing hydrogen that employs a mixture of hydrogen and a hydrocarbon that can both be used as fuel. In one embodiment, the method involves maintaining a mixture including hydrogen and a hydrocarbon in the solid state at ambient pressure and a temperature in excess of about 10 K.

  19. Hydrocarbon potential and exploration methods within cretaceous of Utah-Wyoming overthrust belt: a new frontier in a not-so-old area

    SciTech Connect

    Bertagne, A.J.; Boettcher, J.W.; Vuillermoz, C.

    1986-05-01

    A largely untested stratigraphic play exists within the Cretaceous section of the Utah-Wyoming Overthrust belt. Coarse Cretaceous sediments on the western Absaroka plate merge gradationally eastward into a predominantly shale section, which sets up the potential for Cretaceous sands to pinch out within Cretaceous shale in the Overthrust belt. The discovery well in this play is the Sam Gary Jr. 4-6X Lazeart with a reported initial potential of 87 BOPD from the Upper Cretaceous Frontier Formation. The anticipated source of hydrocarbons is Cretaceous shale - the documented source of most hydrocarbons found to date in the Utah-Wyoming Overthrust belt. Published research indicates that Cretaceous shales have reached adequate maturation levels under the Darby and Absaroka plates and probably on the back of the Absaroka plate. In addition, hydrocarbons may have moved updip from the generation area to shallower reservoirs as a result of secondary migration. Therefore, the geographic area of the play is extensive. State-of-the-art seismic data are an essential prerequisite for systematic exploration of the Cretaceous play. After acquiring a regional seismic grid and tying in well control and surface geology, the following procedure should be implemented: (1) use seismic reflections to establish a regional chronostratigraphic framework, (2) interpret seismic facies to determine geographic distribution of depositional environments, and (3) perform detailed interpretation and forward modeling to locate specific prospects. A reprocessed seismic line from the Overthrust belt confirms that data quality is high enough to use this procedure. An aggressive exploration program in this area is likely to result in significant reserve additions; a commitment to the search for the subtle trap in the Overthrust belt is now needed.

  20. A study of hydrocarbon migration events: Development and application of new methods for constraining the time of migration and an assessment of rock-fluid interactions. Final report, September 1, 1991--August 31, 1994

    SciTech Connect

    Elmore, R.D.; Engel, M.H.

    1993-12-31

    The authors are conducting the research to test and refine a paleomagnetic method for dating hydrocarbon migration, and to assess the chemical alteration of crude oils resulting from fluid-rock interactions. Samples were collected for paleomagnetic and organic geochemical investigations from several units. These include the Old Red Sandstone in Scotland, and the Schoolhouse Member of the Maroon Formation and the Belden Formation in Colorado. Studies of these units are completed or underway. In addition, simulation experiments, where the authors are attempting to form magnetite in the laboratory, are underway.

  1. Apparatus for heat induced separation of hydrocarbon constituents from coal

    SciTech Connect

    Pine, M.; Johnson, J.R.; Moss, R.E.; Sandoval, R.A.

    1984-09-25

    A method and apparatus is provided for accomplishing thermal separation of various hydrocarbons and other compounds from coal, a hydrocarbon rendering module is provided for the continuous agitation and circulation of coal during the rendering period and utilizes thermal trays having stationary and revolving apparatus to improve heat transfer to coal particles and minimize rendering time. Portions of the rendered hydrocarbon products are recycled to the mechanism as an energy source for continuous operation.

  2. Atmospheric hydrocarbon chemistry in central Texas

    NASA Astrophysics Data System (ADS)

    Wittig, Ann Elizabeth

    Hydrocarbon chemistry plays a central role in the determination of the concentrations of ozone, nitrogen oxides and particulate matter in the ambient troposphere. Many years of research have led to a preliminary understanding of the complex chemistry of the thousands of hydrocarbons that are emitted into the atmosphere by biogenic and anthropogenic sources. However, much remains unresolved. This thesis will address several of the unresolved issues in the complex hydrocarbon chemistry that occurs in urban atmospheres. The first portion of this thesis reports atmospheric concentrations of hydrocarbons in Central Texas. These concentrations were compared to hydrocarbon concentrations observed in other urban areas. Probable sources of atmospheric hydrocarbons within Central Texas were identified from spatially resolved hydrocarbon emission inventories. These measurements and identified probable sources suggest the second major portion of the thesis: an analysis of one of the most commonly used source resolution tools, the Chemical Mass Balance (CMB) method. CMB uses linear algebra to identify the sources and source strengths of hydrocarbons in ambient air samples. However, there are several assumptions made by the model to accomplish this task, and these assumptions are believed to impair the model's accuracy. Therefore, the second portion of the thesis characterized the uncertainties associated with the accuracy of CMB, particularly when it was applied to ambient data from Southeast Texas. A multistage box model was constructed to simulate ambient hydrocarbon concentrations in Houston. The box model simulated the inputs of hydrocarbon sources into a hypothetical air mass, while accounting for the unique reactivities of each of the modeled hydrocarbons. The CMB tool was then applied to the data generated by the box model and used to estimate source strengths. The source strengths estimated by CMB were compared to the original inputs to the model. The results indicated

  3. Research on dual-wavelength photometric method for micro liquid volume measurement

    NASA Astrophysics Data System (ADS)

    Wang, Jintao; Liu, Ziyong; Tong, Lin

    2015-02-01

    In order to overcome the shortcoming of significant influence of evaporation capacity on gravimetric method and meet the requirement of online measurement, dual-wavelength photometric method is introduced for measuring microliquid volume. Based on Lambert-Beer law, this paper introduces the dual-wavelength photometric method (DWP method) at 520 nm and 730 nm, which can measure the microliquid volume through the linear relation between the concentration of dilute solution and the absorbance. Comparing to gravimetric method, an experimental system for dual-wavelength photometric method was designed. Experimental results indicate that the test result obtained by using DWP method was better than obtained by using gravimetric method, and met the technical requirement of ISO 8655. Compared with the gravimetric method, the non-gravimetric methods can provide a better solution for microliquid volume measurement, which was less stringent for measurement environment, easy to realize the online calibration and capable of reducing the influence of liquid evaporation.

  4. Comparison of Factorial Kriging Analysis Method and Upward Continuation Filter to Recognize Subsurface Structures - A Case Study: Gravity Data from a Hydrocarbon Field in the Southeast Sedimentary Basins of the East Vietnam Sea

    NASA Astrophysics Data System (ADS)

    Azad, Mohammad-Reza; Koneshloo, Mohammad; Kamakar Rouhani, Abolghasem; Aghajani, Hamid

    2016-04-01

    To interpret geophysical anomaly maps, it is necessary to filter out regional and sometimes noise components. Each measured value in a gravity survey consists of different components. Upward continuation (UC) is one of the most widely used filters. The shortcoming of this filter is not to consider the spatial structure of the data, and also the fact that the trial and error approach and expert's judgment are needed to adjust it. This study aims to compare the factorial kriging analysis (FKA) and UC filters for separation of local and regional anomalies in the gravity data of a hydrocarbon field in the southeast sedimentary basins of the East Vietnam Sea. As shown in this paper, FKA method permits to filter out all of the identified structures, while the UC filter does not possess this capability. Therefore, beside general and classic filtering methods, the FKA method can be used as a strong method in filtering spatial structures and anomaly component.

  5. Using supercritical fluids to refine hydrocarbons

    DOEpatents

    Yarbro, Stephen Lee

    2014-11-25

    This is a method to reactively refine hydrocarbons, such as heavy oils with API gravities of less than 20.degree. and bitumen-like hydrocarbons with viscosities greater than 1000 cp at standard temperature and pressure using a selected fluid at supercritical conditions. The reaction portion of the method delivers lighter weight, more volatile hydrocarbons to an attached contacting device that operates in mixed subcritical or supercritical modes. This separates the reaction products into portions that are viable for use or sale without further conventional refining and hydro-processing techniques. This method produces valuable products with fewer processing steps, lower costs, increased worker safety due to less processing and handling, allow greater opportunity for new oil field development and subsequent positive economic impact, reduce related carbon dioxide, and wastes typical with conventional refineries.

  6. New Geomagnetic and Gravimetric Images of The Chicxulub Impact, Yucatan, Mexico

    NASA Astrophysics Data System (ADS)

    Meyer, U.; Urrutia-Fucugauchi, J.; Rebolledo, M.; Lara, J.

    The GeoForschungsZentrum Potsdam (GFZ) conducted in co-operation with the Uni- versidad Nacional Autónoma de México (UNAM) and the Consejo de Recursos Min- erales (CRM) 17 survey flights over the northern part of the Chicxulub impact struc- ture in the time frame from February 8th to February 24th, 2001. The aerogravimetry system of the GFZ was installed in a Britten-Norman Islander (BN-212), a small twin- engine aircraft so far used only for aeromagnetic surveys of the CRM. All flights in the area of interest were conducted from Mérida. GPS reference stations were installed in Mérida, Progreso and Celestun. The main profiles were flown in E-W-direction with a line spacing of 5 km and N-S-crossings of 30 km. The flight level was 600 ft over wa- ter and 1500 ft over land. The higher flight level on-shore was imperative due to safety regulations and turbulence effects being a compromise between resolution and flight stability. The main goal of the airborne survey was to fly aerogravimetry and aero- magnetometry over the Chicxulub impact structure in the northern part of Yucatán. To the present knowledge, the Chicxulub crater was caused by a meteorite impact about 65 million year before present. It is believed that among other events (large magmatic events in the Dekka region) this impact was mainly responsible for the mass extinction marking the Cretaceous-Tertiary-boundary. The northern part of the impact structure is buried under the sediments and shallow water of the southern Gulf of Mexico. This part is not accessible for research vessels because of its riffs and shoals close to the coast. Consequently, a large data gap remained in the most important, central part of the Chicxulub crater. Therefore, we mapped this area by aerogeophysical means to acquire geomagnetic and gravimetric images of strongly improved quality and resolu- tion. Both new data sets are used to discuss so far existing interpretations and models of the Chicxulub structure. Moreover, a

  7. Viscosity of pure hydrocarbons

    SciTech Connect

    Knapstad, B.; Skjolsvik, P.A.; Oye, H.A.

    1989-01-01

    Accurate viscosity measurements have been performed on eight pure hydrocarbons at atmospheric pressure in the temperature range 20-150/sup 0/C, or up to approximately 20/sup 0/C below the boiling point of the hydrocarbon, by use of an absolute oscillating viscometer. The hydrocarbons are cyclohexane and benzene and the n-alkanes of hexane, heptane, octane, decane, dodecane, and tetradecane. The viscosities are described with a modified Arrhenius equation, and the deviation in fit is 0.12% or less. The accuracy is estimated to be 0.33-0.56%. The lowest viscosities are assumed to have the highest deviation. Literature data reported by Dymond and Young normally fit our viscosities within our estimated accuracy. Other literature viscosities tend to be higher than our results, especially for the n-alkanes.

  8. Prediction of flame velocities of hydrocarbon flames

    NASA Technical Reports Server (NTRS)

    Dugger, Gordon L; Simon, Dorothy M

    1954-01-01

    The laminar-flame-velocity data previously reported by the Lewis Laboratory are surveyed with respect to the correspondence between experimental flame velocities and values predicted by semitheoretical and empirical methods. The combustible mixture variables covered are hydrocarbon structure (56 hydrocarbons), equivalence ratio of fuel-air mixture, mole fraction of oxygen in the primary oxygen-nitrogen mixture (0.17 to 0.50), and initial mixture temperature (200 degrees to 615 degrees k). The semitheoretical method of prediction considered are based on three approximate theoretical equations for flame velocity: the Semenov equation, the Tanford-Pease equation, and the Manson equation.

  9. Prediction of hydrocarbons in sedimentary basins

    USGS Publications Warehouse

    Harff, J.E.; Davis, J.C.; Eiserbeck, W.

    1993-01-01

    To estimate the undiscovered hydrocarbon potential of sedimentary basins, quantitative play assessments specific for each location in a region may be obtained using geostatistical methods combined with the theory of classification of geological objects, a methodology referred to as regionalization. The technique relies on process modeling and measured borehole data as well as probabilistic methods to exploit the relationship between geology (the "predictor") and known hydrocarbon productivity (the "target") to define prospective stratigraphic intervals within a basin. It is demonstrated in case studies from the oil-producing region of the western Kansas Pennsylvanian Shelf and the gas-bearing Rotliegend sediments of the Northeast German Basin. ?? 1993 International Association for Mathematical Geology.

  10. In situ measurement of hydrocarbon fuel concentration near a spark plug in an engine cylinder using the 3.392 µm infrared laser absorption method: application to an actual engine

    NASA Astrophysics Data System (ADS)

    Tomita, Eiji; Kawahara, Nobuyuki; Nishiyama, Atsushi; Shigenaga, Masahiro

    2003-08-01

    An infrared absorption method with a 3.392 µm He-Ne laser was used to determine the hydrocarbon fuel concentration near the spark plug in a spark-ignition engine. Iso-octane was used for the fuel. The pressure and temperature dependence of the molar absorption coefficient was clarified. The molar absorption coefficients of a multi-component fuel such as gasoline were estimated by using the coefficient of each component and considering the mass balance. A sensor was developed and installed in a spark plug, which was substituted in place of an ordinary spark plug in a spark-ignition engine. Light can pass from the sensor through the engine cylinder to measure the fuel concentration. The effects of liquid droplets inside the engine cylinder, mechanical vibrations and other gases such as H2O and CO2 on the measurement accuracy were considered. Four main conclusions were drawn from this study. First, the pressure and temperature effects on the molar absorption coefficient of liquid fuel vapour were determined independently in advance using a constant-volume vessel. The pressure and temperature dependence of the molar absorption coefficient was determined under engine firing conditions. Second, the molar absorption coefficients of a multi-component hydrocarbon fuel such as gasoline were estimated by considering the molar fraction of each component. Third, in situ measurements of the hydrocarbon fuel concentration in an actual engine were obtained using the spark plug sensor and the molar absorption coefficient of iso-octane. The concentration near the spark plug just before ignition was almost in agreement with the mean value that was obtained from the measurement of the flow rate made with a burette, which represented the mean value averaged over many cycles. And fourth, no liquid droplets were observed at near-idling conditions. The effects of other gases, such as CO, CO2 and H2O, can be neglected.

  11. Hydrocarbon fuel detergent

    SciTech Connect

    Meyer, G.R.; Lyons, W.R.

    1990-01-23

    This patent describes a hydrocarbon fuel composition comprising: a hydrocarbon fuel; and a detergent amount of a detergent comprising an alkenylsuccinimide prepared by reacting an alkenylsuccinic acid or anhydride with a mixture of amines, wherein at least 90 weight percent of the alkenyl substituent is derived from an olefin having a carbon chain of from 10 to 30 carbons or mixtures thereof, and wherein the alkenylsuccinic acid or anhydride is reacted with the mixture of amines at a mole ratio of 0.8 to 1.5 moles of the amines per mole of the alkenylsuccinic acid or anhydride.

  12. Absorption of polycyclic aromatic hydrocarbons by Pinus bark: analytical method and use for environmental pollution monitoring in the Palermo area (Sicily, Italy).

    PubMed

    Orecchio, Santino; Gianguzza, Antonio; Culotta, Loredana

    2008-07-01

    In the light of using biomaterial as pollutants sorbents for the environmental biomonitoring, we report here the results of the absorption of polycyclic aromatic hydrocarbons (PAHs) by pine bark. Quantitative analysis of 19 different polycyclic aromatic compounds was performed, after Soxhlet extraction in dichloromethane, by means GC-MS technique. Pinus was chosen due to its wide distribution in the Mediterranean area. The passive absorption of PAH by pine bark in the metropolitan areas allowed us to evaluate the air quality of Palermo. The obtained results showed a very high range of PAHs concentrations, from 33 microg/kg (bark dry weight), as SigmaPAHs, at the control site to 1015 microg/kg along a road with high traffic flow. PMID:18417111

  13. Hydrocarbon contaminated soils and groundwater

    SciTech Connect

    Kostecki, P.T.

    1992-01-01

    This book contains the proceedings of hydrocarbon contaminated soils and groundwater. Topics covered include: Perspectives on hydrocarbon contamination; regulations; environmental fate and modeling; sampling and site assessment; remediation assessment and design; and remediation case studies.

  14. Apparatus for recovering gaseous hydrocarbons from hydrocarbon-containing solid hydrates

    DOEpatents

    Elliott, Guy R. B.; Barraclough, Bruce L.; Vanderborgh, Nicholas E.

    1984-01-01

    A method and apparatus are provided for producing gaseous hydrocarbons from formations comprising solid hydrocarbon hydrates located under either a body of land or a body of water. The vast natural resources of such hydrocarbon hydrates can thus now be economically mined. Relatively warm brine or water is brought down from an elevation above that of the hydrates through a portion of the apparatus and passes in contact with the hydrates, thus melting them. The liquid then continues up another portion of the apparatus, carrying entrained hydrocarbon vapors in the form of bubbles, which can easily be separated from the liquid. After a short startup procedure, the process and apparatus are substantially self-powered.

  15. 21 CFR 178.3530 - Isoparaffinic petroleum hydrocarbons, synthetic.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... hydrocarbons meeting the following specifications: Boiling point 63° -260 °C, as determined by ASTM method D86..., disregarding the last sentence of that procedure. For hydrocarbons boiling below 121 °C, the nonvolatile... Volatile Solvents for Use in Paint, Varnish, Lacquer, and Related Products;” for those boiling above 121...

  16. 21 CFR 178.3530 - Isoparaffinic petroleum hydrocarbons, synthetic.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... hydrocarbons meeting the following specifications: Boiling point 63° -260 °C, as determined by ASTM method D86..., disregarding the last sentence of that procedure. For hydrocarbons boiling below 121 °C, the nonvolatile... Volatile Solvents for Use in Paint, Varnish, Lacquer, and Related Products;” for those boiling above 121...

  17. 21 CFR 178.3530 - Isoparaffinic petroleum hydrocarbons, synthetic.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... hydrocarbons meeting the following specifications: Boiling point 63° -260 °C, as determined by ASTM method D86..., disregarding the last sentence of that procedure. For hydrocarbons boiling below 121 °C, the nonvolatile... Volatile Solvents for Use in Paint, Varnish, Lacquer, and Related Products;” for those boiling above 121...

  18. Optrode for sensing hydrocarbons

    DOEpatents

    Miller, H.; Milanovich, F.P.; Hirschfeld, T.B.; Miller, F.S.

    1987-05-19

    A two-phase system employing the Fujiwara reaction is provided for the fluorometric detection of halogenated hydrocarbons. A fiber optic is utilized to illuminate a column of pyridine trapped in a capillary tube coaxially attached at one end to the illuminating end of the fiber optic. A strongly alkaline condition necessary for the reaction is maintained by providing a reservoir of alkali in contact with the column of pyridine, the surface of contact being adjacent to the illuminating end of the fiber optic. A semipermeable membrane caps the other end of the capillary tube, the membrane being preferentially permeable to the halogenated hydrocarbon but preferentially impermeable to water and pyridine. As the halogenated hydrocarbon diffuses through the membrane and into the column of pyridine, fluorescent reaction products are formed. Light propagated by the fiber optic from a light source, excites the fluorescent products. Light from the fluorescence emission is also collected by the same fiber optic and transmitted to a detector. The intensity of the fluorescence gives a measure of the concentration of the halogenated hydrocarbons. 6 figs.

  19. Optrode for sensing hydrocarbons

    DOEpatents

    Miller, H.; Milanovich, F.P.; Hirschfeld, T.B.; Miller, F.S.

    1988-09-13

    A two-phase system employing the Fujiwara reaction is provided for the fluorometric detection of halogenated hydrocarbons. A fiber optic is utilized to illuminate a column of pyridine trapped in a capillary tube coaxially attached at one end to the illuminating end of the fiber optic. A strongly alkaline condition necessary for the reaction is maintained by providing a reservoir of alkali in contact with the column of pyridine, the surface of contact being adjacent to the illuminating end of the fiber optic. A semipermeable membrane caps the other end of the capillary tube, the membrane being preferentially permeable to the halogenated hydrocarbon and but preferentially impermeable to water and pyridine. As the halogenated hydrocarbon diffuses through the membrane and into the column of pyridine, fluorescent reaction products are formed. Light propagated by the fiber optic from a light source, excites the fluorescent products. Light from the fluorescence emission is also collected by the same fiber optic and transmitted to a detector. The intensity of the fluorescence gives a measure of the concentration of the halogenated hydrocarbons. 5 figs.

  20. Zeroing in on hydrocarbons

    SciTech Connect

    Roest, I.P.B. van der; Brasser, D.J.S.; Wagebaert, A.P.J.; Stam, P.H.

    1997-05-01

    The increasing costs of remediating contaminated sites has stimulated research for cost-reducing techniques in soil investigation and cleanup techniques. MAP Environmental Research has developed a technology using ground penetrating radar in combination with in house developed software to locate and define the extent of hydrocarbon contamination. This article discusses the new technology. 2 figs.

  1. Excited states in hydrocarbons

    SciTech Connect

    Lipsky, S.

    1987-01-01

    In this brief review we first summarize some pertinent features of the photophysical properties of excited states of hydrocarbons and the mechanisms by which they transfer energy to solutes and then review their yields and their behavior under fast-electron irradiation conditions. 33 refs.

  2. Optrode for sensing hydrocarbons

    DOEpatents

    Miller, Holly; Milanovich, Fred P.; Hirschfeld, Tomas B.; Miller, Fred S.

    1988-01-01

    A two-phase system employing the Fujiwara reaction is provided for the fluorometric detection of halogenated hydrocarbons. A fiber optic is utilized to illuminate a column of pyridine trapped in a capillary tube coaxially attached at one end to the illuminating end of the fiber optic. A strongly alkaline condition necessary for the reaction is maintained by providing a reservoir of alkali in contact with the column of pyridine, the surface of contact being adjacent to the illuminating end of the fiber optic. A semipermeable membrane caps the other end of the capillary tube, the membrane being preferentially permeable to the halogenated hydrocarbon and but preferentially impermeable to water and pyridine. As the halogenated hydrocarbon diffuses through the membrane and into the column of pyridine, fluorescent reaction products are formed. Light propagated by the fiber optic from a light source, excites the fluorescent products. Light from the fluorescence emission is also collected by the same fiber optic and transmitted to a detector. The intensity of the fluorescence gives a measure of the concentration of the halogenated hydrocarbons.

  3. Optrode for sensing hydrocarbons

    DOEpatents

    Miller, Holly; Milanovich, Fred P.; Hirschfeld, Tomas B.; Miller, Fred S.

    1987-01-01

    A two-phase system employing the Fujiwara reaction is provided for the fluorometric detection of halogenated hydrocarbons. A fiber optic is utilized to illuminate a column of pyridine trapped in a capillary tube coaxially attached at one end to the illuminating end of the fiber optic. A strongly alkaline condition necessary for the reaction is maintained by providing a reservoir of alkali in contact with the column of pyridine, the surface of contact being adjacent to the illuminating end of the fiber optic. A semipermeable membrane caps the other end of the capillary tube, the membrane being preferentially permeable to the halogenated hydrocarbon and but preferentially impermeable to water and pyridine. As the halogenated hydrocarbon diffuses through the membrane and into the column of pyridine, fluorescent reaction products are formed. Light propagated by the fiber optic from a light source, excites the fluorescent products. Light from the fluorescence emission is also collected by the same fiber optic and transmitted to a detector. The intensity of the fluorescence gives a measure of the concentration of the halogenated hydrocarbons.

  4. Hydrocarbon options emerge

    SciTech Connect

    Fairley, P.

    1995-11-01

    Europe stole the scene at last week`s International Chlorofluorocarbon (CFC) and Halon Alternatives Conference in Washington as attendees learned more about an accelerating shift to low-cost hydrocarbon refrigerants by European equipment manufacturers. Udo Wenning, representing German refrigerator market leader Bosch-Siemens, told the conference that hydrocarbons-isobutane as refrigerant and cyclopentane to blow the insulating foam-are now used in 90% of German production. Wenning says that in all performance parameters, hydrocarbons match the hydrochlorofluorocarbon (HCFC) and hydrofluorocarbon (HFC) replacements favored in the U.S. and Japan and that, unlike HCFCs and HFCs they have low global warming potential. Their Achille`s heel is flammability, Wenning says. American equipment manufacturers aiming to sell a new generation of equipment designed for the new HFC refrigerants sought to amplify concern over flammability at the conference. {open_quotes}In a society as litigious as ours, we do not see a future for flammable refrigerants,{close_quotes} says a representative of air conditioner manufacturer Carrier. Hydrocarbon supporters such as Greenpeace say the risks are mananageable.

  5. Certification of new Pb iCRM (Candidate ERM-38xx series) via Gravimetric Isotope Mixtures and MC-ICP-MS Measurements

    NASA Astrophysics Data System (ADS)

    Ponzevera, E.; Quetel, C. R.

    2008-12-01

    Lead is known to be a particularly toxic chemical element. Mining and smelting of Pb and its domestic use over the centuries have contaminated the surface of Earth and jeopardized the health of humans, domestic animals and wildlife. Omnipresence of Pb has however an advantage. It can be used as an isotopic tracer of pollution sources and pathways in the environment. Pb isotopic Certified Reference Materials (iCRM) with undisputed characteristics are then required to validate Pb isotope ratio measurements. The materials currently available worldwide were produced in the 1960's by the National Bureau of Standards (now NIST, USA) and are now the object of polemics regarding the accuracy of some of the accompanying certified values. Moreover, new materials with lower relative uncertainty statements are demanded by users. This presentation is centred on the production and the certification at the EC-JRC-Institute for Reference Materials and Measurements of a new series of Pb iCRM (candidate ERM-38xx series). The production included six Pb gravimetric isotope mixtures, a common Pb material dedicated to routine calibration work and a series of four 207Pb slightly enriched natural-like Pb materials for the validation of the δ-scale method below 0.01%. The gravimetric isotope mixtures method, originally supported by mass spectrometry measurements performed on GS-MS or TI-MS instruments, was applied successfully to MC-ICP-MS. The measurements and certification methods we developed were validated in several ways, including a systematic investigation on possible significant sources of uncertainty and comparisons of results obtained by different laboratories on identical samples. Relative uncertainties on isotope ratios obtained for the newly produced Pb iCRM are as low as 0.017%, which is between 2 and 4 times smaller than the uncertainties carried by the NIST-981 material. Going below 0.01% was not possible mainly because of uncompressible uncertainties coming from the

  6. Venus clouds: test for hydrocarbons.

    PubMed

    Plummer, W T

    1969-03-14

    Infrared reflection spectra of hydrocarbon clouds and frosts now give a critical test of Velikovsky's prediction that Venus is surrounded by a dense envelope of hydrocarbon clouds and dusts. Venus does not exhibit an absorption feature near 2.4 microns, although such a feature is prominent in every hydrocarbon spectrum observed.

  7. Source identification of petroleum hydrocarbons in soil and sediments from Iguaçu River Watershed, Paraná, Brazil using the CHEMSIC method (CHEMometric analysis of Selected Ion Chromatograms).

    PubMed

    Gallotta, Fabiana D C; Christensen, Jan H

    2012-04-27

    A chemometric method based on principal component analysis (PCA) of pre-processed and combined sections of selected ion chromatograms (SICs) is used to characterise the hydrocarbon profiles in soil and sediment from Araucária, Guajuvira, General Lúcio and Balsa Nova Municipalities (Iguaçu River Watershed, Paraná, Brazil) and to indicate the main sources of hydrocarbon pollution. The study includes 38 SICs of polycyclic aromatic compounds (PACs) and four of petroleum biomarkers in two separate analyses. The most contaminated samples are inside the Presidente Getúlio Vargas Refinery area. These samples represent a petrogenic pattern and different weathering degrees. Samples from outside the refinery area are either less or not contaminated, or contain mixtures of diagenetic, pyrogenic and petrogenic inputs where different proportions predominate. The locations farthest away from industrial activity (Balsa Nova) contains the lowest levels of PAC contamination. There are no evidences to conclude positive matches between the samples from outside the refinery area and the Cusiana spilled oil.

  8. Autothermal reforming of aliphatic and aromatic hydrocarbon liquids

    NASA Technical Reports Server (NTRS)

    Flytzani-Stephanopoulos, M.; Voecks, G. E.

    1983-01-01

    Results are presented from a study of the autothermal reforming of paraffins and aromatics over nickel catalysts. The trials were performed to examine the carbon products that appear when steam is passed over hydrocarbon liquids to form H2-rich gases, i.e., the autothermal process (ATR). Attention was given to n-hexane, n-tetradecane, benzene, and benzene solutions of naphthalene with reactant preheat to 1000-1150 F. The carbon-formation limit was sought as a function of the steam-to-carbon and oxygen to carbon molar ratios at constant pressure and the preheat temperatures. The catalyst bed was examined after each trial to identify the locations and types of carbon formed using SEM, thermal gravimetric analysis, and X ray diffraction techniques. The hydrocarbon fuels each had a separate temperature and reaction profile, as well as carbon formation characteristics. No carbon formation was observed in the upper layer of the reactor bed, while both gas phase and surface-grown deposits were present in the lower part. The results are concluded of use in the study of No. 2 fuel oil for ATR feedstock.

  9. Application of thermal desorption to the development of a gas chromatographic/mass spectrometric method for the determination of toluene, chlorinated aromatic hydrocarbons, and 2,3,7,8-tetrachlorodibenzo-p-dioxin in combustion emissions.

    PubMed

    Donaldson, John D; Grimes, Susan M; Mehta, Lina; Jafari, Ahmad J

    2003-01-01

    A fast and accurate analytical method, which uses commercially available adsorbents (Tenax TA, Carbotrap B and C, and Carbosieve S-III), was developed for the sampling and determination of aromatic hydrocarbons, chloroaromatic compounds, and 2,3,7,8-tetrachlorodibenzo-p-dioxin. The breakthrough volume data show that Carbotrap C has a good capacity for compounds of high molecular weight, whereas Carbosieve S-III and Tenax TA are efficient for volatile compounds. The organic components are thermally desorbed and transferred to a gas chromatograph/mass spectrometer. Importantly, thermal desorption avoids conventional solvent extraction procedures and also allows reuse of adsorbent tubes. Preliminary results for recovery of analytes from tubes packed with single adsorbent prove that a single-adsorbent bed is not capable of sampling a wide range of compounds. The best method to obtain the desired collection and desorption properties is to use adsorbent tubes containing several different materials. The results of optimization studies are summarized. PMID:12607738

  10. Mantle hydrocarbons: abiotic or biotic?

    PubMed

    Sugisaki, R; Mimura, K

    1994-06-01

    Analyses of 227 rocks from fifty localities throughout the world showed that mantle derived rocks such as tectonized peridotites in ophiolite sequences (tectonites) arid peridotite xenoliths in alkali basalts contain heavier hydrocarbons (n-alkanes), whereas igneous rocks produced by magmas such as gabbro arid granite lack them. The occurrence of hydrocarbons indicates that they were not derived either from laboratory contamination or from held contamination; these compounds found in the mantle-derived rocks are called here "mantle hydrocarbons." The existence of hydrocarbons correlates with petrogenesis. For example, peridotite cumulates produced by magmatic differentiation lack hydrocarbons whereas peridotite xenoliths derived from the mantle contain them. Gas chromatographic-mass spectrometric records of the mantle hydrocarbons resemble those of aliphatics in meteorites and in petroleum. Features of the hydrocarbons are that (a) the mantle hydrocarbons reside mainly along grain boundaries and in fluid inclusions of minerals; (b) heavier isoprenoids such as pristane and phytane are present; and (c) delta 13C of the mantle hydrocarbons is uniform (about -27%). Possible origins for the mantle hydrocarbons are as follows. (1) They were in organically synthesized by Fischer-Tropsch type reaction in the mantle. (2) They were delivered by meteorites and comets to the early Earth. (3) They were recycled by subduction. The mantle hydrocarbons in the cases of (1) and (2) are abiogenic and those in (3) are mainly biogenic. It appears that hydrocarbons may survive high pressures and temperatures in the mantle, but they are decomposed into lighter hydrocarbon gases such as CH4 at lower pressures when magmas intrude into the crust; consequently, peridotite cumulates do not contain heavier hydrocarbons but possess hydrocarbon gases up to C4H10. PMID:11541663

  11. Mantle hydrocarbons: Abiotic or biotic?

    SciTech Connect

    Sugisaki, Ryuichi; Mimura, Koichi

    1994-06-01

    Analyses of 227 rocks from fifty localities throughout the world showed that mantle derived rocks such as tectonized peridotites in ophiolite sequences (tectonites) and peridotite xenoliths in alkali basalts contain heavier hydrocarbons (n-alkanes), whereas igneous rocks produced by magmas such as gabbro and granite lack them. The occurrence of hydrocarbons indicates that they were not derived either from laboratory contamination or from field contamination; these compounds found in the mantle-derived rocks are called here {open_quotes}mantle hydrocarbons.{close_quotes} The existence of hydrocarbons correlates with petrogenesis. For example, peridotite cumulates produced by magmatic differentiation lack hydrocarbons whereas peridotite xenoliths derived from the mantle contain them. Gas chromatographic-mass spectrometric records of the mantle hydrocarbons resemble those of aliphatics in meteorites and in petroleum. Features of the hydrocarbons are that (a) the mantle hydrocarbons reside mainly along grain boundaries and in fluid inclusions of minerals; (b) heavier isoprenoids such as pristane and phytane are present; and (c) {delta}{sup 13}C of the mantle hydrocarbons is uniform (about {minus}27{per_thousand}). Possible origins for the mantle hydrocarbons are as follows. (1) They were inorganically synthesized by Fischer-Tropsch type reaction in the mantle. (2) They were delivered by meteorites and comets to the early Earth. (3) They were recycled by subduction. The mantle hydrocarbons in the cases of (1) and (2) are abiogenic and those in (3) are mainly biogenic. It appears that hydrocarbons may survive high pressures and temperatures in the mantle, but they are decomposed into lighter hydrocarbon gases such as CH{sub 4} at lower pressures when magmas intrude into the crust; consequently, peridotite cumulates do not contain heavier hydrocarbons but possess hydrocarbon gases up to C{sub 4}H{sub 10}. 76 refs., 5 figs., 3 tabs.

  12. Mantle hydrocarbons: abiotic or biotic?

    PubMed

    Sugisaki, R; Mimura, K

    1994-06-01

    Analyses of 227 rocks from fifty localities throughout the world showed that mantle derived rocks such as tectonized peridotites in ophiolite sequences (tectonites) arid peridotite xenoliths in alkali basalts contain heavier hydrocarbons (n-alkanes), whereas igneous rocks produced by magmas such as gabbro arid granite lack them. The occurrence of hydrocarbons indicates that they were not derived either from laboratory contamination or from held contamination; these compounds found in the mantle-derived rocks are called here "mantle hydrocarbons." The existence of hydrocarbons correlates with petrogenesis. For example, peridotite cumulates produced by magmatic differentiation lack hydrocarbons whereas peridotite xenoliths derived from the mantle contain them. Gas chromatographic-mass spectrometric records of the mantle hydrocarbons resemble those of aliphatics in meteorites and in petroleum. Features of the hydrocarbons are that (a) the mantle hydrocarbons reside mainly along grain boundaries and in fluid inclusions of minerals; (b) heavier isoprenoids such as pristane and phytane are present; and (c) delta 13C of the mantle hydrocarbons is uniform (about -27%). Possible origins for the mantle hydrocarbons are as follows. (1) They were in organically synthesized by Fischer-Tropsch type reaction in the mantle. (2) They were delivered by meteorites and comets to the early Earth. (3) They were recycled by subduction. The mantle hydrocarbons in the cases of (1) and (2) are abiogenic and those in (3) are mainly biogenic. It appears that hydrocarbons may survive high pressures and temperatures in the mantle, but they are decomposed into lighter hydrocarbon gases such as CH4 at lower pressures when magmas intrude into the crust; consequently, peridotite cumulates do not contain heavier hydrocarbons but possess hydrocarbon gases up to C4H10.

  13. Catalysts for synthesizing various short chain hydrocarbons

    DOEpatents

    Colmenares, Carlos

    1991-01-01

    Method and apparatus (10), including novel photocatalysts, are disclosed for the synthesis of various short chain hydrocarbons. Light-transparent SiO.sub.2 aerogels doped with photochemically active uranyl ions (18) are fluidized in a fluidized-bed reactor (12) having a transparent window (16), by hydrogen and CO, C.sub.2 H.sub.4 or C.sub.2 H.sub.6 gas mixtures (20), and exposed to radiation (34) from a light source (32) external to the reactor (12), to produce the short chain hydrocarbons (36).

  14. [Storage of hydrocarbon-degrading bacteria].

    PubMed

    Bade, G M; Vecchioli, G I; del Panno, M T; Painceira, M T

    1994-01-01

    The storage in the laboratory of hydrocarbon degrading bacteria to be used in the decontamination of polluted sites or in the enhancement of biological treatment of industrial effluents was studied. Storage was carried out at 4 degrees C in nutrient agar and in a medium with selection pressure, liquid mineral medium with hydrocarbons. Storage at 4 degrees C with selection pressure and storage at -20 degrees C of 7 gram negative bacilli were compared. The former was the easiest method for preserving the greatest number of strains viable and active. PMID:7838975

  15. [Storage of hydrocarbon-degrading bacteria].

    PubMed

    Bade, G M; Vecchioli, G I; del Panno, M T; Painceira, M T

    1994-01-01

    The storage in the laboratory of hydrocarbon degrading bacteria to be used in the decontamination of polluted sites or in the enhancement of biological treatment of industrial effluents was studied. Storage was carried out at 4 degrees C in nutrient agar and in a medium with selection pressure, liquid mineral medium with hydrocarbons. Storage at 4 degrees C with selection pressure and storage at -20 degrees C of 7 gram negative bacilli were compared. The former was the easiest method for preserving the greatest number of strains viable and active.

  16. Bacterial sources for phenylalkane hydrocarbons

    SciTech Connect

    Ellis, L.; Winans, R.E.; Langworthy, T.

    1996-10-01

    The presence of phenylalkane hydrocarbons in geochemical samples has been the source of much controversy. Although an anthropogenic input from detergent sources always appears likely, the distribution of phenylalkane hydrocarbons in some cases far exceeding that attributed to detergent input has led to a reappraisal of this view. Indeed, recent work involving analysis of the lipid hydrocarbon extracts from extant Thermoplasma bacteria has revealed the presence of phenylalkane hydrocarbons. The presence of phenylalkane hydrocarbons in sedimentary organic matter may therefore represent potential biological markers for thermophilic bacteria.

  17. Heating hydrocarbon containing formations in a line drive staged process

    DOEpatents

    Miller, David Scott

    2009-07-21

    Method for treating a hydrocarbon containing formation are described herein. Methods may include providing heat to a first section of the formation with one or more first heaters in the first section. First hydrocarbons may be heated in the first section such that at least some of the first hydrocarbons are mobilized. At least some of the mobilized first hydrocarbons may be produced through a production well located in a second section of the formation. The second section may be located substantially adjacent to the first section. A portion of the second section may be provided some heat from the mobilized first hydrocarbons, but is not conductively heated by heat from the first heaters. Heat may be provided to the second section with one or more second heaters in the second section to further heat the second section.

  18. Increased concentrations of polycyclic aromatic hydrocarbons in Alpine streams during annual snowmelt: investigating effects of sampling method, site characteristics, and meteorology.

    PubMed

    Shahpoury, Pourya; Hageman, Kimberly J; Matthaei, Christoph D; Alumbaugh, Robert E; Cook, Michelle E

    2014-10-01

    Silicone passive samplers and macroinvertebrates were used to measure time-integrated concentrations of polycyclic aromatic hydrocarbons (PAHs) in alpine streams during annual snowmelt. The three sampling sites were located near a main highway in Arthur's Pass National Park in the Southern Alps of New Zealand. A similar set of PAH congeners, composed of 2-4 rings, were found in silicone passive samplers and macroinvertebrates. The background PAH concentrations were similar at all sites, implying that proximity to the highway did not affect concentrations. In passive samplers, an increase of PAH concentrations by up to seven times was observed during snowmelt. In macroinvertebrates, the concentration changes were moderate; however, macroinvertebrate sampling did not occur during the main pulse observed in the passive samplers. The extent of vegetation in the catchment appeared to affect the concentration patterns seen at the different stream sites. A strong correlation was found between PAH concentrations in passive samplers and the amount of rainfall in the study area, indicating that the washout of contaminants from snowpack by rainfall was an important process.

  19. Influence of the method of production of eggs on the daily intake of polycyclic aromatic hydrocarbons and organochlorine contaminants: an independent study in the Canary Islands (Spain).

    PubMed

    Luzardo, Octavio P; Rodríguez-Hernández, Angel; Quesada-Tacoronte, Yohana; Ruiz-Suárez, Norberto; Almeida-González, Maira; Henríquez-Hernández, Luis Alberto; Zumbado, Manuel; Boada, Luis D

    2013-10-01

    Analysis of 16 polycyclic aromatic hydrocarbons (PAHs), 20 organochlorine pesticides (OCPs) and 18 polychlorinated biphenyls (PCBs) were performed on eggs from three different production types (conventional, free-run and organic) collected from the markets of the Canary Islands (Spain). Unlike other studies we did not found differences in the content of PCBs or OCPs of eggs in relation to its production type. Median ∑OCPs content was 3.87 ng g⁻¹ fat, being dieldrin, dicofol, hexachlorobenzene, p,p'-DDE and p,p'-DDT the most frequently detected. Median ∑PCBs value was 3.93 ng g⁻¹ fat, with 79.9% of this amount coming from the marker PCBs. Two samples, one free-run and one organic, greatly exceeded the current European Commission (EC) limit of 2.5 pg TEQ(PCDD/F) g⁻¹ lipid, but the rest were well below of this limit. The concentrations of PAHs in conventionally produced eggs were almost 4 times higher than in free-run or organic eggs. Mean dietary intake estimates of the organochlorine contaminants based on consumption of eggs, regardless of the type chosen, is negligible for the Canary Islands' population. However, the median dietary intake estimates of PAHs greatly depend on the type of eggs chosen, being much lower when free-run and organic eggs are consumed.

  20. Influence of the method of production of eggs on the daily intake of polycyclic aromatic hydrocarbons and organochlorine contaminants: an independent study in the Canary Islands (Spain).

    PubMed

    Luzardo, Octavio P; Rodríguez-Hernández, Angel; Quesada-Tacoronte, Yohana; Ruiz-Suárez, Norberto; Almeida-González, Maira; Henríquez-Hernández, Luis Alberto; Zumbado, Manuel; Boada, Luis D

    2013-10-01

    Analysis of 16 polycyclic aromatic hydrocarbons (PAHs), 20 organochlorine pesticides (OCPs) and 18 polychlorinated biphenyls (PCBs) were performed on eggs from three different production types (conventional, free-run and organic) collected from the markets of the Canary Islands (Spain). Unlike other studies we did not found differences in the content of PCBs or OCPs of eggs in relation to its production type. Median ∑OCPs content was 3.87 ng g⁻¹ fat, being dieldrin, dicofol, hexachlorobenzene, p,p'-DDE and p,p'-DDT the most frequently detected. Median ∑PCBs value was 3.93 ng g⁻¹ fat, with 79.9% of this amount coming from the marker PCBs. Two samples, one free-run and one organic, greatly exceeded the current European Commission (EC) limit of 2.5 pg TEQ(PCDD/F) g⁻¹ lipid, but the rest were well below of this limit. The concentrations of PAHs in conventionally produced eggs were almost 4 times higher than in free-run or organic eggs. Mean dietary intake estimates of the organochlorine contaminants based on consumption of eggs, regardless of the type chosen, is negligible for the Canary Islands' population. However, the median dietary intake estimates of PAHs greatly depend on the type of eggs chosen, being much lower when free-run and organic eggs are consumed. PMID:23939041

  1. Membrane separation of hydrocarbons

    DOEpatents

    Chang, Y. Alice; Kulkarni, Sudhir S.; Funk, Edward W.

    1986-01-01

    Mixtures of heavy oils and light hydrocarbons may be separated by passing the mixture through a polymeric membrane. The membrane which is utilized to effect the separation comprises a polymer which is capable of maintaining its integrity in the presence of hydrocarbon compounds and which has been modified by being subjected to the action of a sulfonating agent. Sulfonating agents which may be employed will include fuming sulfuric acid, chlorosulfonic acid, sulfur trioxide, etc., the surface or bulk modified polymer will contain a degree of sulfonation ranging from about 15 to about 50%. The separation process is effected at temperatures ranging from about ambient to about 100.degree. C. and pressures ranging from about 50 to about 1000 psig.

  2. Hydrocarbon bioremediation -- An overview

    SciTech Connect

    Reisinger, H.J.

    1995-12-31

    Bioremediation is the process that transforms xenobiotics introduced into the environment to a less toxic or innocuous form, or mineralizes them to inorganic species. The processes can be carried out through either aerobic or anaerobic pathways by indigenous heterotrophs or by specially engineered organisms. For some xenobiotics, the process can also be carried out by cometabolic processes, which use another compound as the carbon and energy source. This technique can be applied either in situ or ex situ. An overview is presented of real-world applications of a variety of hydrocarbon bioremediation approaches, including biopiling, bioventing, bioslurping, landfarming, electrobioreclamation, and biovertical circulation wells. Problems in translating laboratory and field-scale pilot test data to full-scale operating systems are discussed. Such issues include biodegradation enhancement, nutrient and electron acceptor delivery, alternative electron acceptors, and integration of biological, chemical, and physical approaches to hydrocarbon remediation.

  3. FROZEN HYDROCARBONS IN COMETS

    SciTech Connect

    Simonia, Irakli

    2011-02-15

    Recent investigations of the luminescence of frozen hydrocarbon particles of icy cometary halos have been carried out. The process of luminescence of organic icy particles in a short-wavelength solar radiation field is considered. A comparative analysis of observed and laboratory data leads to 72 luminescent emission lines in the spectrum of the comet 153P/Ikeya-Zhang. The concept of cometary relict matter is presented, and the creation of a database of unidentified cometary emission lines is proposed.

  4. Direct hydrocarbon fuel cells

    DOEpatents

    Barnett, Scott A.; Lai, Tammy; Liu, Jiang

    2010-05-04

    The direct electrochemical oxidation of hydrocarbons in solid oxide fuel cells, to generate greater power densities at lower temperatures without carbon deposition. The performance obtained is comparable to that of fuel cells used for hydrogen, and is achieved by using novel anode composites at low operating temperatures. Such solid oxide fuel cells, regardless of fuel source or operation, can be configured advantageously using the structural geometries of this invention.

  5. Site characterization and petroleum hydrocarbon plume mapping

    SciTech Connect

    Ravishankar, K.

    1996-12-31

    This paper presents a case study of site characterization and hydrocarbon contamination plume mapping/delineation in a gas processing plant in southern Mexico. The paper describes innovative and cost-effective use of passive (non-intrusive) and active (intrusive) techniques, including the use of compound-specific analytical methods for site characterization. The techniques used, on a demonstrative basis, include geophysical, geochemical, and borehole drilling. Geochemical techniques used to delineate the horizontal extent of hydrocarbon contamination at the site include soil gas surveys. The borehole drilling technique used to assess the vertical extent of contamination and confirm geophysical and geochemical data combines conventional hollow-stem auguring with direct push-probe using Geoprobe. Compound-specific analytical methods, such as hydrocarbon fingerprinting and a modified method for gasoline range organics, demonstrate the inherent merit and need for such analyses to properly characterize a site, while revealing the limitations of noncompound-specific total petroleum hydrocarbon analysis. The results indicate that the techniques used in tandem can properly delineate the nature and extent of contamination at a site; often supplement or complement data, while reducing the risk of errors and omissions during the assessment phase; and provide data constructively to focus site-specific remediation efforts. 7 figs.

  6. Assessing dry density and gravimetric water content of soils in geotechnics with complex conductivity measurements : preliminary investigations

    NASA Astrophysics Data System (ADS)

    Kaouane, C.; Beck, Y.; Fauchard, C.; Chouteau, M.

    2012-12-01

    Quality controls of geotechnical works need gravimetric water content (w) and dry density (γd) measurements. Afterwards, results are compared to Proctor tests and referred to soil classification. Depending on the class of soils, different objectives must be achieved. Those measurements are usually carried out with neutron and gamma probes. Combined use of theses probes directly access (w, γd). Theses probes show great disadvantages as: nuclear hazard, heavy on-site, transporation and storage restrictions and low sampling volumes. Last decades showed a strong development of electrical and electromagnetic methods for mapping water content in soils. Still, their use in Geotechnics is limited due to interfacial effects neglected in common models but strong in compacted soils. We first showed that (w, γd) is equivalent to (φ, Sr) assuming density of particles γs=2.7 (g.cm-3). This assumption is true for common soils used in civil engineering. That first relationship allows us to work with meaningful parameters for geophysicists. Revil&Florsh recently adapted Vinegar&Waxman model for Spectal Induced Polarization (SIP) measurements at low frequencies (<50 kHz). This model relates quantitatively the electrical double layer polarization at the surface of grains. It takes into account saturation, porosity and granulometry. Standard granulometry and mineralogy are generally available in geotechnical campaigns. In-phase conductivity would be mostly related to saturation as quadrature conductivity would be related to porosity and surface conductivity. Although this model was developed for oil-bearing sands, we investigated its potential for compacted soils. Former DC-resistivity (ρ) measurements were carried out on a silty fined-grained soil (A1 in GTR classification or ML-CL in USCS) in a cylindrical cell (radius ~4 cm, heigth 7 cm). Median diameter of grain was 50 μm. For each measurement, samples were compacted at Proctor energy. We assessed (w, γd) by weighting and

  7. Endothermic hydrocarbon upgrading process

    SciTech Connect

    Harandi, M.N.; Owen, H.

    1990-08-21

    This patent describes a process for upgrading aliphatic hydrocarbons to aromatic hydrocarbons. It comprises: burning a hydrogen-deficient fuel under oxygen-deficient conditions to evolve a hot gas containing essentially no oxygen; providing an aromatization reaction zone containing a zeolite catalyst; directly transferring a quantity of thermal energy from the hot flue gas to the aromatization reaction zone by flowing hot flue gas through the aromatization reaction zone; contacting an aliphatic hydrocarbon feedstream with the zeolite catalyst under primary conversion conditions in the aromatization reaction zone to evolve an aromatization reaction zone effluent stream containing aromatics; withdrawing the aromatization reaction zone effluent stream from the aromatization zone; separating the aromatization reaction zone effluent stream into a product stream, a secondary conversion feedstream comprising CO, CO{sub 2}, and H{sub i} and a stream containing C{sub 3}-C{sub 5} aliphatics; and charging the secondary conversion feedstream to a methanol synthesis reaction zone to convert at least a portion of the secondary conversion feedstream to methanol.

  8. Endothermic hydrocarbon upgrading process

    SciTech Connect

    Harandi, M.N.; Owen, H.

    1991-07-09

    This patent describes a process for upgrading aliphatic hydrocarbons to aromatic hydrocarbons. It comprises burning a hydrogen-deficient fuel under oxygen-deficient conditions to evolve a hot flue gas containing essentially no oxygen; providing an aromatization reaction zone containing a zeolite catalyst; directly transferring a quantity of thermal energy from the hot flue gas to the aromatization reaction zone by flowing hot flue gas through the aromatization reaction zone, the quantity of thermal energy being sufficient to supply the endothermic heat of reaction to aromatize at least a portion of the aliphatic feedstream; contacting an aliphatic hydrocarbon feedstream with the zeolite catalyst under primary conversion conditions in the aromatization reaction zone to evolve an aromatization reaction zone effluent stream containing aromatics; withdrawing the aromatization reaction zone effluent stream from the aromatization reaction zone; separating the aromatization reaction zone effluent stream into a product stream, a secondary conversion feedstream comprising CO, CO{sub 2}, and H{sub 2} and a stream containing C{sub 3}-C{sub 5} aliphatics; and charging the secondary conversion feedstream.

  9. Detection of new hydrocarbon reservoir using hydrocarbon microtremor combined attribute analysis

    NASA Astrophysics Data System (ADS)

    Ramadhan, Dimmas; Nugraha, Andri Dian; Afnimar, Akbar, Muhammad Fadhillah; Mulyanagara, Guntur

    2013-09-01

    An increasing demand for oil and gas production undoubtedly triggered innovation in exploration studies to find new hydrocarbon reservoir. Low-frequency passive seismic method named Hy MAS (Hydrocarbon Microtremor Analysis) is a new method invented and developed recently by Spectraseis which provide a quick look to find new hydrocarbon reservoir prospect area. This method based on empirical study which investigated an increasing of spectra anomaly between 2 - 4 Hz above reservoir but missing from the measurement distant from the reservoir. This method is quite promising because it has been used as another DHI (Direct Hydrocarbon Indicator) instead of active seismic survey which has some problem when applied in sensitive biomes. Another advantage is this method is completely passive and does not require seismic artificial excitation sources. In this study, by utilizing many attributes mentioned in the latest publication of this method, we try to localize new hydrocarbon prospect area outside from the proven production field. We deployed 63 stations of measurement with two of them are located above the known reservoir production site. We measured every single attribute for each data acquired from all station and mapped it spatially for better understanding and interpretation. The analysis has been made by considering noise identification from the measurement location and controlled by the attribute values from the data acquired by two stations above the reservoir. As the result, we combined each attribute analysis and mapped it in weighted-scoring map which provide the level of consistency for every single attribute calculated in each station. Finally, the new reservoir location can be suggested by the station which has a weighted-score around the values from the two production reservoir stations. We successfully identified 5 new stations which expected to have good prospect of hydrocarbon reservoir.

  10. Radical scavengers from heavy hydrocarbons

    SciTech Connect

    Kubo, Junichi

    1996-10-01

    The hydrogen-donating properties of some hydrocarbons form the basis for processes such as coal liquefaction and heavy oil upgrading. However, these hydrocarbons have seldom been used for other purposes, because their potential applications have not been well recognized. Research has indicated that these hydrogen-donating hydrocarbons can be used in important reactions as radical scavengers and have properties particular to those of pure hydrocarbons without functional groups containing heteroatoms. Over years of study researchers have found that pure hydrocarbons with radical-scavenging effects nearly as high as those in conventional hindered phenolic antioxidants can be produced from petroleum, and these hydrogen-donating hydrocarbons exhibit such effects even in oxidative atmospheres (i.e., they function as antioxidants). He has also shown that these mixtures have some properties particular to pure hydrocarbons without functional groups containing heteroatoms, and they`ve seen that a mechanism based on the steric effects appears when these hydrocarbons are used in heavy oil hydroprocessing. Hydrogen-donating hydrocarbons should be a viable resource in many applications. In this article, he presents radical-scavenging abilities, characteristics as pure hydrocarbons, and applications on the basis of the studies.

  11. Characterizing the transplanar and in-plane water transport of textiles with gravimetric and image analysis technique: Spontaneous Uptake Water Transport Tester.

    PubMed

    Tang, K P M; Wu, Y S; Chau, K H; Kan, C W; Fan, J T

    2015-04-15

    Water absorption and transport property of textiles is important since it affects wear comfort, efficiency of treatment and functionality of product. This paper introduces an accurate and reliable measurement tester, which is based on gravimetric and image analysis technique, for characterising the transplanar and in-plane wicking property of fabrics. The uniqueness of this instrument is that it is able to directly measure the water absorption amount in real-time, monitor the direction of water transport and estimate the amount of water left on skin when sweating. Throughout the experiment, water supply is continuous which simulates profuse sweating. Testing automation could even minimise variation caused by subjective manipulation, thus enhancing testing accuracy. This instrument is versatile in terms of the fabrics could be tested. A series of shirting fabrics made by different fabric structure and yarn were investigated and the results show that the proposed method has high sensitivity in differentiating fabrics with varying geometrical differences. Fabrics with known hydrophobicity were additionally tested to examine the sensitivity of the instrument. This instrument also demonstrates the flexibility to test on high performance moisture management fabrics and these fabrics were found to have excellent transplanar and in-plane wicking properties.

  12. Electrochemical evaluation of the corrosion behaviour for structural steel SAE 1005 exposed to two different atmospheres (urban and industrial) and comparison with atmospheric corrosion gravimetric measurements

    NASA Astrophysics Data System (ADS)

    Salas, Y.; Guerrero, L.; Castiblanco, H.; Torres, C.; Palacios, A.

    2016-02-01

    The Atmospheric corrosion is a phenomenon we see every day in our environment that arises due to environmental pollution we generate, there is currently very little information on atmospheric corrosion in the department of Boyacá and in general, in Colombia. The aim of this paper is to analyse which of these two environments is more aggressive and wherein the steel corrodes faster. To analyse these phenomenon specimens made in steel SAE 105 exposed for five months to the atmosphere in the municipalities of Tunja and Nobsa (an urban atmosphere and other industrial atmosphere) were installed, a control was carried to verify the amount of time that will be exposed each of these samples to the atmosphere, of Thus it may determine the lifetime of a structural steel. For the analysis of these samples electrochemical tests were carried out to calculate the rate of corrosion and resistance to polarization, also the gravimetric method be conducted to compare what was the amount of mass lost during the time of exposure to each of the samples.

  13. Development of a supercritical fluid extraction-gas chromatography-mass spectrometry method for the identification of highly polar compounds in secondary organic aerosols formed from biogenic hydrocarbons in smog chamber experiments.

    PubMed

    Chiappini, L; Perraudin, E; Durand-Jolibois, R; Doussin, J F

    2006-11-01

    A new one-step method for the analysis of highly polar components of secondary organic aerosols (SOA) has been developed. This method should lead to a better understanding of SOA formation and evolution since it enables the compounds responsible for SOA formation to be identified. Since it is based on supercritical fluid extraction coupled to gas chromatography-mass spectrometry, it minimizes the analysis time and significantly enhances sensitivity, which makes it suitable for trace-level compounds, which are constituents of SOA. One of the key features of this method is the in situ derivatisation step: an online silylation allowing the measurement of highly polar, polyfunctional compounds, which is a prerequisite for the elucidation of chemical mechanisms. This paper presents the development of this analytical method and highlights its ability to address this major atmospheric issue through the analysis of SOA formed from the ozonolysis of a biogenic hydrocarbon (sabinene). Ozonolysis of sabinene was performed in a 6 m3 Teflon chamber. The aerosol components were derivatised in situ. More than thirty products, such as sabinaketone, sabinic acid and other multifunctional compounds including dicarboxylic acids and oxoacids, were measured. Nine of them were identified and quantified. The sensitivity and the linearity (0.91method were both good and detection limits ranged from 1.2 to 6.4 ng for the investigated compounds.

  14. A validated liquid chromatographic method for the determination of polycyclic aromatic hydrocarbons in honey after homogeneous liquid-liquid extraction using hydrophilic acetonitrile and sodium chloride as mass separating agent.

    PubMed

    Koltsakidou, Anastasia; Zacharis, Constantinos K; Fytianos, Konstantinos

    2015-01-16

    In the present report, a simple and cost-effective method for the determination of twelve US EPA priority polycyclic aromatic hydrocarbons (PAHs) in honey samples after salting-assisted liquid-liquid extraction and UHPLC with fluorescence detection is proposed. The sample treatment is based on the usage of hydrophilic acetonitrile as extraction solvent and its phase separation under high salinity conditions. Due to the high sugar content of the samples the phase separation is promoted effortlessly. Several parameters affecting the extraction efficiency and method sensitivity including the concentration of the honey samples, the type and volume of the extraction solvent, the type and quantity of the inorganic salt, extraction time and centrifugation time was systematically investigated. The method was validated in-house according to the Commission Decision 2002/657/EC guidelines. The limit of detection (LOD) of the method lay between 0.02 and 0.04ngmL(-1) (corresponding to 0.08 and 0.16ngg(-1)) which are close to the quality criteria established by European Regulation (EC) 836/2011 concerning the PAHs in foodstuffs. The mean analytical bias (expressed as relative recoveries) in all spiking levels was acceptable being in the range of 54-118% while the relative standard deviation (RSD) was lower than 19%. The proposed method has been satisfactorily applied for the analysis of the selected PAHs residues in various honey samples obtained from Greek region.

  15. Determination of Total Petroleum Hydrocarbons (TPH) Using Total Carbon Analysis

    SciTech Connect

    Ekechukwu, A.A.

    2002-05-10

    Several methods have been proposed to replace the Freon(TM)-extraction method to determine total petroleum hydrocarbon (TPH) content. For reasons of cost, sensitivity, precision, or simplicity, none of the replacement methods are feasible for analysis of radioactive samples at our facility. We have developed a method to measure total petroleum hydrocarbon content in aqueous sample matrixes using total organic carbon (total carbon) determination. The total carbon content (TC1) of the sample is measured using a total organic carbon analyzer. The sample is then contacted with a small volume of non-pokar solvent to extract the total petroleum hydrocarbons. The total carbon content of the resultant aqueous phase of the extracted sample (TC2) is measured. Total petroleum hydrocarbon content is calculated (TPH = TC1-TC2). The resultant data are consistent with results obtained using Freon(TM) extraction followed by infrared absorbance.

  16. Chromatographic detection and analysis of traces of hydrocarbons

    NASA Technical Reports Server (NTRS)

    Fickey, E. W.; Mullins, H. E.

    1969-01-01

    Special analytical column having in series two separate absorption sections charged with beads of porous polymer and a sample of gas detects traces of hydrocarbons. New method requires only 15 minutes for execution.

  17. Li{sub 4}FeH{sub 6}: Iron-containing complex hydride with high gravimetric hydrogen density

    SciTech Connect

    Saitoh, Hiroyuki; Takagi, Shigeyuki; Matsuo, Motoaki; Aoki, Katsutoshi; Iijima, Yuki; Endo, Naruki; Orimo, Shin-ichi

    2014-07-01

    Li{sub 4}FeH{sub 6}, which has the highest gravimetric hydrogen density of iron-containing complex hydrides reported so far, is synthesized by hydrogenation of a powder mixture of iron and LiH above 6.1 GPa at 900 °C. In situ synchrotron radiation X-ray diffraction measurements reveal that while kinetics require high temperature and thus high pressure for the synthesis, Li{sub 4}FeH{sub 6} is expected to be thermodynamically stable slightly below room temperature at ambient pressure; further synthetic studies to suppress the kinetic effects may enable us to synthesize Li{sub 4}FeH{sub 6} at moderate pressures. Li{sub 4}FeH{sub 6} can be recovered at ambient conditions where Li{sub 4}FeH{sub 6} is metastable.

  18. Electromagnetic, magnetic, and gravimetric surveys at the Bi'r Jarbuah gold prospect, Kingdom of Saudi Arabia

    USGS Publications Warehouse

    Miller, C.H.; Showail, A.A.; Bazzari, M.A.; Khoja, J.A.; Hajour, M.O.

    1990-01-01

    A detailed search for gold and associated minerals was begun in the Bi'r Jarbuah area in 1988. Crone electromagnetic (CEM), magnetic, and gravimetric surveys were run in the areas of greatest interest. Anomalous areas are most interesting in the southern part of the area where linear magnetic and gravity anomalies trend east-northeast and overlap in large part. They are most prominent at or near the south end of a diorite pluton where some quartz veins mined by the ancients also trend northeast. A second area, at the extreme southern end of the survey, contains a large CEM anomaly that coincides with northeast-trending magnetic and gravity anomalies. Although this second area is largely overlain by alluvium, a major quartz vein strikes to the northeast in the adjacent bedrock.

  19. Detailed geoid computations for GEOS-C altimeter experiment areas. [gravimetric geoid for Atlantic and northeast Pacific Ocean areas

    NASA Technical Reports Server (NTRS)

    Marsh, J. G.; Vincent, S.

    1973-01-01

    The GEOS-C spacecraft is scheduled to carry onboard a radar altimeter for the purpose of measuring the geoid undulations in oceanic areas. An independently derived geoid map will provide a valuable complement to these experiments. A detailed gravimetric geoid is presented for the Atlantic and northeast Pacific Ocean areas based upon a combination of the Goddard Space Flight Center GEM-6 earth model and surface 1 deg x 1 deg gravity data. As part of this work a number of satellite derived gravity models were evaluated to establish the model which best represented the long wave length features of the geoid in the above mentioned area. Comparisons of the detailed geoid with the astrogeodetic data provided by the National Ocean Survey and dynamically derived tracking station heights indicate that the accuracy of this combined geoid is on the order of 2 meters or better where data was dense and 5 to 7 meters where data was less dense.

  20. Susceptibility of a polycaprolactone-based root canal filling material to degradation. II. Gravimetric evaluation of enzymatic hydrolysis.

    PubMed

    Tay, Franklin R; Pashley, David H; Yiu, Cynthia K Y; Yau, Joyce Y Y; Yiu-fai, Mak; Loushine, Robert J; Weller, R Norman; Kimbrough, W Frank; King, Nigel M

    2005-10-01

    Polycaprolactone is susceptible to enzymatic biodegradation via ester bond cleavage. This study examined the susceptibility of Resilon, a polycaprolactone-based root filling material to enzymatic hydrolysis. Resilon, gutta-percha, and polycaprolactone disks, prepared by compression molding, were incubated in phosphate-buffered saline, lipase PS or cholesterol esterase at 37 degrees C for 96 h. They were retrieved at different time intervals for gravimetric analysis and scanning electron microscopy. The materials exhibited slight weight gains when incubated in phosphate-buffered saline that can be attributed to water sorption. Gutta-percha showed similar weight gains in the two enzymes. Conversely, Resilon and polycaprolactone exhibited extensive surface thinning and weight losses after incubation in lipase PS and cholesterol esterase. Glass filler particles in Resilon were exposed following surface dissolution of the polymer matrix, creating rough surface topography. Biodegradation of Resilon by bacterial and salivary enzymes warrants further investigation of their activities using cultures of endodontically relevant microbes and human saliva extracts.

  1. Application of gamma-ray radiography and gravimetric measurements after accelerated corrosion tests of steel embedded in mortar

    SciTech Connect

    Duffó, Gustavo; Gaillard, Natalia; Mariscotti, Mario; Ruffolo, Marcelo

    2015-08-15

    The accelerated corrosion by the impressed current technique is widely used in studies of concrete durability since it has the advantage that tests can be carried out within reasonable periods of time. In the present work the relationship between the applied current density and the resulting damage on the reinforcing steel, by applying optical microscopy, scanning electron microscopy, gamma-ray radiography and gravimetric measurements, was studied by means of the implementation of accelerated corrosion tests on reinforced mortar. The results show that the efficiency of the applied current is between 1 and 77%, regardless of the applied current density, the water/cement ratio and the mortar cover depth of the specimens. The results show the applicability of the gamma-ray radiography technique to detect localized corrosion of steel rebars in laboratory specimens.

  2. Evaluation of gravimetric ground truth soil moisture data collected for the agricultural soil moisture experiment, 1978 Colby, Kansas, aircraft mission

    NASA Technical Reports Server (NTRS)

    Arya, L. M.; Phinney, D. E. (Principal Investigator)

    1980-01-01

    Soil moisture data acquired to support the development of algorithms for estimating surface soil moisture from remotely sensed backscattering of microwaves from ground surfaces are presented. Aspects of field uniformity and variability of gravimetric soil moisture measurements are discussed. Moisture distribution patterns are illustrated by frequency distributions and contour plots. Standard deviations and coefficients of variation relative to degree of wetness and agronomic features of the fields are examined. Influence of sampling depth on observed moisture content an variability are indicated. For the various sets of measurements, soil moisture values that appear as outliers are flagged. The distribution and legal descriptions of the test fields are included along with examinations of soil types, agronomic features, and sampling plan. Bulk density data for experimental fields are appended, should analyses involving volumetric moisture content be of interest to the users of data in this report.

  3. Vmh2 hydrophobin layer entraps glucose: A quantitative characterization by label-free optical and gravimetric methods

    NASA Astrophysics Data System (ADS)

    Della Ventura, B.; Rea, I.; Caliò, A.; Giardina, P.; Gravagnuolo, A. M.; Funari, R.; Altucci, C.; Velotta, R.; De Stefano, L.

    2016-02-01

    Hydrophobins (HFBs) are peculiar proteins which self-assemble at hydrophilic-hydrophobic interfaces into amphipathic membranes, and some of them (class I HFB) are able to form much more stable amyloid-like layers. This feature makes them suitable for many purposes, particularly when stable surface functionalization is required, also in view of their versatility in binding different kinds of molecules. For instance, it has been shown that Vmh2 from Pleurotus ostreatus (a class I HFB) is able to bind molecules like glucose, thus offering the perspective of using Vmh2 as a surface functionalization tool in bio-hybrid devices. In this paper a quantitative analysis of glucose interaction with the Vmh2 layer is reported; in particular, it is shown that Vmh2 layer swells by almost doubling its thickness as a result of glucose diffusion and each Vmh2 monomer is able to bind approximately 30 glucose molecules. These results have been achieved by self-assembling multi-layers of Vmh2 on a gold substrate and, subsequently, measuring both the mass of the bound glucose and the thickness of the resulting layer through two different and complementary techniques: quartz crystal-microbalance and ellipsometry. The data provided by the two techniques are in a satisfactory agreement and offer a plausible description of the mechanisms underlying the interaction of glucose with Vmh2 layer. This facile and versatile coating is of interest for biomedical applications of gold surfaces and particles.

  4. Analysis of hydrocarbons generated in coalbeds

    NASA Astrophysics Data System (ADS)

    Butala, Steven John M.

    This dissertation describes kinetic calculations using literature data to predict formation rates and product yields of oil and gas at typical low-temperature conditions in coalbeds. These data indicate that gas formation rates from hydrocarbon thermolysis are too low to have generated commercial quantities of natural gas, assuming bulk first-order kinetics. Acid-mineral-catalyzed cracking, transition-metal-catalyzed hydrogenolysis of liquid hydrocarbons, and catalyzed CO2 hydrogenation form gas at high rates. The gaseous product compositions for these reactions are nearly the same as those for typical natural coalbed gases, while those from thermal and catalytic cracking are more representative of atypical coalbed gases. Three Argonne Premium Coals (Upper-Freeport, Pittsburgh #8 and Lewiston-Stockton) were extracted with benzene in both Soxhlet and elevated pressure extraction (EPE) systems. The extracts were compared on the basis of dry mass yield and hydrocarbon profiles obtained by gas chromatography/mass spectrometry. The dry mass yields for the Upper-Freeport coal gave consistent results by both methods, while the yields from the Pittsburgh #8 and Lewiston-Stockton coals were greater by the EPE method. EPE required ˜90 vol. % less solvent compared to Soxhlet extraction. Single-ion-chromatograms of the Soxhlet extracts all exhibited bimodal distributions, while those of the EPE extracts did not. Hydrocarbons analyzed from Greater Green River Basin samples indicate that the natural oils in the basin originated from the coal seams. Analysis of artificially produced oil indicates that hydrous pyrolysis mimics generation of C15+ n-alkanes, but significant variations were found in the branched alkane, low-molecular-weight n-alkanes, and high-molecular-weight aromatic hydrocarbon distributions.

  5. Bioremediation of hydrocarbon-contaminated polar soils.

    PubMed

    Aislabie, Jackie; Saul, David J; Foght, Julia M

    2006-06-01

    Bioremediation is increasingly viewed as an appropriate remediation technology for hydrocarbon-contaminated polar soils. As for all soils, the successful application of bioremediation depends on appropriate biodegradative microbes and environmental conditions in situ. Laboratory studies have confirmed that hydrocarbon-degrading bacteria typically assigned to the genera Rhodococcus, Sphingomonas or Pseudomonas are present in contaminated polar soils. However, as indicated by the persistence of spilled hydrocarbons, environmental conditions in situ are suboptimal for biodegradation in polar soils. Therefore, it is likely that ex situ bioremediation will be the method of choice for ameliorating and controlling the factors limiting microbial activity, i.e. low and fluctuating soil temperatures, low levels of nutrients, and possible alkalinity and low moisture. Care must be taken when adding nutrients to the coarse-textured, low-moisture soils prevalent in continental Antarctica and the high Arctic because excess levels can inhibit hydrocarbon biodegradation by decreasing soil water potentials. Bioremediation experiments conducted on site in the Arctic indicate that land farming and biopiles may be useful approaches for bioremediation of polar soils.

  6. Volatile hydrocarbons and fuel oxygenates: Chapter 12

    USGS Publications Warehouse

    Cozzarelli, Isabelle M.

    2014-01-01

    Petroleum hydrocarbons and fuel oxygenates are among the most commonly occurring and widely distributed contaminants in the environment. This chapter presents a summary of the sources, transport, fate, and remediation of volatile fuel hydrocarbons and fuel additives in the environment. Much research has focused on the transport and transformation processes of petroleum hydrocarbons and fuel oxygenates, such as benzene, toluene, ethylbenzene, and xylenes and methyl tert‐butyl ether, in groundwater following release from underground storage tanks. Natural attenuation from biodegradation limits the movement of these contaminants and has received considerable attention as an environmental restoration option. This chapter summarizes approaches to environmental restoration, including those that rely on natural attenuation, and also engineered or enhanced remediation. Researchers are increasingly combining several microbial and molecular-based methods to give a complete picture of biodegradation potential and occurrence at contaminated field sites. New insights into the fate of petroleum hydrocarbons and fuel additives have been gained by recent advances in analytical tools and approaches, including stable isotope fractionation, analysis of metabolic intermediates, and direct microbial evidence. However, development of long-term detailed monitoring programs is required to further develop conceptual models of natural attenuation and increase our understanding of the behavior of contaminant mixtures in the subsurface.

  7. Treatment of petroleum hydrocarbon polluted environment through bioremediation: a review.

    PubMed

    Singh, Kriti; Chandra, Subhash

    2014-01-01

    Bioremediation play key role in the treatment of petroleum hydrocarbon contaminated environment. Exposure of petroleum hydrocarbon into the environment occurs either due to human activities or accidentally and cause environmental pollution. Petroleum hydrocarbon cause many toxic compounds which are potent immunotoxicants and carcinogenic to human being. Remedial methods for the treatment of petroleum contaminated environment include various physiochemical and biological methods. Due to the negative consequences caused by the physiochemical methods, the bioremediation technology is widely adapted and considered as one of the best technology for the treatment of petroleum contaminated environment. Bioremediation utilizes the natural ability of microorganism to degrade the hazardous compound into simpler and non hazardous form. This paper provides a review on the role of bioremediation in the treatment of petroleum contaminated environment, discuss various hazardous effects of petroleum hydrocarbon, various factors influencing biodegradation, role of various enzymes in biodegradation and genetic engineering in bioremediation.

  8. Process for separating an ethylenically unsaturated hydrocarbon from a hydrocarbon mixture

    SciTech Connect

    vanEijl, A.T.

    1986-06-24

    A process is described for separating an ethylenically unsaturated hydrocarbon from a hydrocarbon mixture characterized by: (a) distilling a hydrocarbon mixture containing the unsaturated hydrocarbon with an N-(aminoalkyl) piperazine; and (b) separating the amine/hydrocarbon mixture into at least two factions, one of which contains the amine and the unsaturated hydrocarbon.

  9. Chemical contamination and transformation of soils in hydrocarbon production regions

    NASA Astrophysics Data System (ADS)

    Zamotaev, I. V.; Ivanov, I. V.; Mikheev, P. V.; Nikonova, A. N.

    2015-12-01

    The current concepts of soil pollution and transformation in the regions of hydrocarbon production have been reviewed. The development of an oil field creates extreme conditions for pedogenesis. Tendencies in the radial migration, spatial distribution, metabolism, and accumulation of pollutants (oil, oil products, and attendant heavy metals) in soils of different bioclimatic zones have been analyzed. The radial and lateral mobility of pollution halos is a universal tendency in the technogenic transformation of soils and soil cover in the regions of hydrocarbon production. The biodegradation time of different hydrocarbon compounds strongly varies under different landscape conditions, from several months to several tens of years. The transformation of original (mineral and organic) soils to their technogenic modifications (mechanically disturbed, chemically contaminated, and chemo soils and chemozems) occurs in the impact zone of technogenic hydrocarbon fluxes under any physiographical conditions. The integrated use of the existing methods for the determination of the total content and qualitative composition of bituminous substances and polyaromatic hydrocarbons in combination with the chromatographic determination of normal alkanes and hydrocarbon gases, as well as innovative methods of studies, allows revealing new processes and genetic relationships in soils and studying the functioning of soils and soil cover. The study of the hydrocarbon contamination of soils is important for development of restoration measures and lays the groundwork for the ecological and hygienic regulation based on the zonation of soil and landscape resistance to different pollutants.

  10. Comparative study for determination of some polycyclic aromatic hydrocarbons 'PAHs' by a new spectrophotometric method and multivariate calibration coupled with dispersive liquid-liquid extraction.

    PubMed

    Abdel-Aziz, Omar; El Kosasy, A M; El-Sayed Okeil, S M

    2014-12-10

    A modified dispersive liquid-liquid extraction (DLLE) procedure coupled with spectrophotometric techniques was adopted for simultaneous determination of naphthalene, anthracene, benzo(a)pyrene, alpha-naphthol and beta-naphthol in water samples. Two different methods were used, partial least-squares (PLS) method and a new derivative ratio method, namely extended derivative ratio (EDR). A PLS-2 model was established for simultaneous determination of the studied pollutants in methanol, by using twenty mixtures as calibration set and five mixtures as validation set. Also, in methanol a novel (EDR) method was developed for determination of the studied pollutants, where each component in the mixture of the five PAHs was determined by using a mixture of the other four components as divisor. Chemometric and EDR methods could be also adopted for determination of the studied PAH in water samples after transferring them from aqueous medium to the organic one by utilizing dispersive liquid-liquid extraction technique, where different parameters were investigated using a full factorial design. Both methods were compared and the proposed method was validated according to ICH guidelines and successfully applied to determine these PAHs simultaneously in spiked water samples, where satisfactory results were obtained. All the results obtained agreed with those of published methods, where no significant difference was observed. PMID:24934969

  11. Moving hydrocarbons through portions of tar sands formations with a fluid

    DOEpatents

    Stegemeier, George Leo; Mudunuri, Ramesh Raju; Vinegar, Harold J.; Karanikas, John Michael; Jaiswal, Namit; Mo, Weijian

    2010-05-18

    A method for treating a tar sands formation is disclosed. The method includes heating a first portion of a hydrocarbon layer in the formation from one or more heaters located in the first portion. The heat is controlled to increase a fluid injectivity of the first portion. A drive fluid and/or an oxidizing fluid is injected and/or created in the first portion to cause at least some hydrocarbons to move from a second portion of the hydrocarbon layer to a third portion of the hydrocarbon layer. The second portion is between the first portion and the third portion. The first, second, and third portions are horizontally displaced from each other. The third portion is heated from one or more heaters located in the third portion. Hydrocarbons are produced from the third portion of the formation. The hydrocarbons include at least some hydrocarbons from the second portion of the formation.

  12. Process for producing benzene by hydrodealkylation of a hydrocarbon fraction comprising alkylaromatic hydrocarbons, olefinic hydrocarbons and sulfur compound

    SciTech Connect

    Derrien, M.; Cosyns, J.

    1984-07-31

    A stabilized hydrocarbon fraction comprising toluene, xylene, sulfur and olefinic hydrocarbons is converted to benzene by catalytic hydrodesulfurization, hydrodealkylation and catalytic hydrogenation.

  13. A magnetic-based dispersive micro-solid-phase extraction method using the metal-organic framework HKUST-1 and ultra-high-performance liquid chromatography with fluorescence detection for determining polycyclic aromatic hydrocarbons in waters and fruit tea infusions.

    PubMed

    Rocío-Bautista, Priscilla; Pino, Verónica; Ayala, Juan H; Pasán, Jorge; Ruiz-Pérez, Catalina; Afonso, Ana M

    2016-03-01

    A hybrid material composed by the metal-organic framework (MOF) HKUST-1 and Fe3O4 magnetic nanoparticles (MNPs) has been synthetized in a quite simple manner, characterized, and used in a magnetic-assisted dispersive micro-solid-phase extraction (M-d-μSPE) method in combination with ultra-high-performance liquid chromatography (UHPLC) and fluorescence detection (FD). The application was devoted to the determination of 8 heavy polycyclic aromatic hydrocarbons (PAHs) in different aqueous samples, specifically tap water, wastewaters, and fruit tea infusion samples. The overall M-d-μSPE-UHPLC-FD method was optimized and validated. The method is characterized by: its simplicity in both the preparation of the hybrid material (simple mixing) and the magnetic-assisted approach (∼10min extraction time), the use of low sorbent amounts (20mg of HKUST-1 and 5mg of Fe3O4 MNPs), and the low organic solvent consumption in the overall M-d-μSPE-UHPLC-FD method (1.5mL of acetonitrile in the M-d-μSPE method and 2.8mL of acetonitrile in the UHPLC-FD run). The resulting method has high sensitivity, with LODs down to 0.8ngL(-1); adequate intermediate precision, with relative standard deviation values (RSD) always lower than 6.3% (being the range 5.9-9.0% in tap water for a spiked level of 45ngL(-1), 6.1-14% in wastewaters for a spiked level of 45ngL(-1), and 7.2-17% in fruit tea infusion samples for a spiked level of 45ngL(-1)); and adequate relative recoveries, with average values of 82% in tap water, and 94% and 75% in wastewater and fruit tea infusion samples, respectively, if using the proper matrix-matched calibration.

  14. Thermophysical Properties of Hydrocarbon Mixtures

    National Institute of Standards and Technology Data Gateway

    SRD 4 NIST Thermophysical Properties of Hydrocarbon Mixtures (PC database for purchase)   Interactive computer program for predicting thermodynamic and transport properties of pure fluids and fluid mixtures containing up to 20 components. The components are selected from a database of 196 components, mostly hydrocarbons.

  15. Integral Approaches to Determine Sub-Crustal Stress from Terrestrial Gravimetric Data

    NASA Astrophysics Data System (ADS)

    Eshagh, Mehdi

    2016-03-01

    The spherical harmonic expressions of the horizontal sub-crustal stress components induced by the mantle convection are convergent only to low degrees. In this paper, we use the method of stress (S) function with numerical differentiation and present a formula for determining the degree of convergence from the mean Moho depth. We found that for the global mean Moho depth, 23 km, this convergence degree is 622 and for Iran, 35 km, it is 372. Also, three methods are developed and applied for computing the sub-crustal stress, (1) direct integration with a spectral kernel limited up to the degree of convergence, (2) integral inversion with a kernel having closed-form formula without any frequency limit, and (3) solving an integral equation with limited spectral kernel to the convergence degree. The second method has no divergence problem and its kernel function is well behaving so that the system of equations from which the S function is determined is stable, and no regularisation is needed to solve it. It should be noted that for using this method the resolution of the recovery should be higher than 0.5° × 0.5°, otherwise the recovered S function and correspondingly the stress components will have smaller magnitude than those derived from the other two methods. Our numerical studies for stress recovery in Iran and its surrounding areas show that the methods, which use the limited spectral kernels to the convergence degree, deliver consistent results to that of the spherical harmonic expansion.

  16. Diterpenoid tetracyclic hydrocarbons of petroleum

    SciTech Connect

    Vorob'eva, N.S.; Zemskova, Z.K.; Pekh, T.I.; Petrov, A.A.

    1987-08-01

    Diterpenoid hydrocarbons are fairly widespread in various caustobioliths. However, if petroleums contain mainly acyclic diterpenoids (phytane, pristane and norpristane), cyclic diterpaenes such as fichtelite, pimarane, iosene (kaurane) and hibbane are often found in hydrocarbons isolated from coal and shale. Recent advances in the chemistry of diterpenoids isolated from caustobioliths, are described in a separate paper. Much less is known about petroleum polycyclic diterpenoid hydrocarbons, particularly those with four saturated rings. A series of tetracyclic hydrocarbons C/sub 19/H/sub 32/ (molar mass 260), found in a number of light petroleums and gas condensates from the Jura deposits of Central Kara-Kum (Turkmen S.S.R.), are examined here. These hydrocarbons are present in petroleums and condensates from the Davaly, Erden, Ortakak, Southern Beuideshik deposits, they are always identical and occur in the same ratios. The composition of the tretracyclanes isolated from the Ortakak gas condensates (well 17) will be examined in detail.

  17. Hydrocarbon sensors and materials therefor

    DOEpatents

    Pham, Ai Quoc; Glass, Robert S.

    2000-01-01

    An electrochemical hydrocarbon sensor and materials for use in sensors. A suitable proton conducting electrolyte and catalytic materials have been found for specific application in the detection and measurement of non-methane hydrocarbons. The sensor comprises a proton conducting electrolyte sandwiched between two electrodes. At least one of the electrodes is covered with a hydrocarbon decomposition catalyst. Two different modes of operation for the hydrocarbon sensors can be used: equilibrium versus non-equilibrium measurements and differential catalytic. The sensor has particular application for on-board monitoring of automobile exhaust gases to evaluate the performance of catalytic converters. In addition, the sensor can be utilized in monitoring any process where hydrocarbons are exhausted, for instance, industrial power plants. The sensor is low cost, rugged, sensitive, simple to fabricate, miniature, and does not suffer cross sensitivities.

  18. UV Raman spectroscopy of hydrocarbons.

    PubMed

    Loppnow, G R; Shoute, L; Schmidt, K J; Savage, A; Hall, R H; Bulmer, J T

    2004-11-15

    In this paper, the UV Raman spectra of a large number of saturated and alkyl-substituted monocyclic, bicyclic and polycyclic aromatic hydrocarbons are obtained at 220 and 233 nm excitation wavelengths. Also included are nitrogen- and sulphur-containing hydrocarbons. The spectra obtained are fluorescence free, even for such highly fluorescent compounds as perylene, consistent with earlier reports of UV Raman spectra of hydrocarbons. The hydrocarbon UV Raman spectra exhibit greatly improved signal-to-noise ratio when in the neat liquid or solution state compared with the neat solid state, suggesting that some surface degradation occurs under the conditions used here. Assignments are given for most of the bands and clear marker bands for the different classes of hydrocarbons are readily observable, although their relative intensities vary greatly. These results are discussed in the context of structure and symmetry to develop a consistent, molecular-based model of vibrational group frequencies. PMID:15482987

  19. Biomonitoring method for the determination of polycyclic aromatic hydrocarbons in hair by online in-tube solid-phase microextraction coupled with high performance liquid chromatography and fluorescence detection.

    PubMed

    Yamamoto, Yusuke; Ishizaki, Atsushi; Kataoka, Hiroyuki

    2015-09-01

    Polycyclic aromatic hydrocarbons (PAHs) are formed from the incomplete combustion or pyrolysis of organic matter during industrial processing and various human activities, but human exposure to PAHs has not yet been elucidated in detail. To assess long-term exposure to PAHs, we developed a simple and sensitive method for measuring PAHs in hair by online in-tube solid-phase microextraction using a CP-Sil 19CB capillary column as an extraction device, followed by high-performance liquid chromatography using a Zorbax Eclipse PAH column and fluorescence detection. Seventeen PAHs could be analyzed simultaneously, with good linearity from 20 to 1000pg/mL each as determined using stable isotope-labeled PAH internal standards. The detection limits of PAHs were 0.5-20.4pg/mL. PAHs in human hair samples were extracted by ultrasonication in 50mM NaOH in methanol, and successfully analyzed without any interference peaks, with good recovery rates above 70% in spiked hair samples. Using this method, we evaluated the suitability of using hair PAHs as biomarkers for long-term exposure. PMID:26245363

  20. Development of an analytical method for the simultaneous determination of 15 carcinogenic polycyclic aromatic hydrocarbons and polycyclic aromatic nitrogen heterocyclic compounds. application to diesel particulates.

    PubMed

    Sauvain, J J; Vu Duc, T; Huynh, C K

    2001-12-01

    A new method enabling the determination of 15 priority carcinogenic polyaromatic compounds (PAC) proposed by the US National Toxicology Program (NTP) has been developed and applied to diesel exhaust particulates (DEP). The clean-up procedure consists of solid-phase extraction (SPE) and HPLC fractionation on silica phases followed by liquid-liquid extraction and chromatography on a polyvinylbenzene copolymer column. The method gives good recoveries for all PAC studied except dibenzo[a,j]acridine and dibenzo[a,h]pyrene, for which recovery values are below 80%. The use of GC-MS ion trap and its capacity to achieve single-ion storage enhanced the sensitivity of the method, enabling the detection of high-molecular-weight PAH in the low ng g(-1) concentration range. Intermediate polarity GC columns, e.g. BPX-50 or equivalent, enabled better separation, when applied to DEP analysis, than the generally used DB-5 apolar phase. This is observed mainly for separation of isomeric compounds belonging to the benzofluoranthene and dibenzopyrene families. The application of this method to DEP sampled from the exhaust of a diesel engine and in confined locations such as a tunnel has shown that all PAH of the NTP list could be detected, except dibenzo[a,h]pyrene. No dibenzacridine or dibenzocarbazole could be detected in such matrices. The method is sufficiently sensitive to be applicable to environmental exposure measurements in occupational health surveys.