Science.gov

Sample records for btp supported liquid

  1. Selective recovery of minor trivalent actinides from high level liquid waste by R-BTP/SiO2-P adsorbents

    NASA Astrophysics Data System (ADS)

    Sano, Yuichi; Surugaya, Naoki; Yamamoto, Masahiko

    2010-03-01

    Concerning the selective recovery of minor trivalent actinides (MA(III) = Am(III) and Cm(III)) from high level liquid waste (HLLW) by extraction chromatography, adsorption and elution behaviours of MA(III) and fission products (FP) in a nitric acid media were studied using iHex-BTP/SiO2-P adsorbents, which is expected to show high adsorption affinity for MA(III) even in concentrated HNO3 solution, such as HLLW. In the batch experiments, Pd showed strong adsorption on iHex-BTP/SiO2-P adsorbents under any concentration of HNO3. The MA(III) and heavy Ln(III) (Sm(III), Eu(III) and Gd(III)) were also adsorbed at the condition of high HNO3 concentration, but they showed no adsorption under low HNO3concentration. The separation factor for MA(III)/heavy Ln(III) took the maximum value (over 100) at around 1mol/dm3 HNO3. It was difficult to elute MA(III) or heavy Ln(III) selectively by HNO3 from the iHex-BTP/SiO2-P adsorbents degradated by γ-ray irradiation. The chromatographic separation of real HLLW by an iHex-BTP/SiO2-P column showed that MA(III) could be recovered selectively by adjusting the acidity of the feed solution, i.e. HLLW, to 1mol/dm3 and using H2O as eluant. The adsorption of Pd(II) can be decreased by the addition of appropriate complexing reagents, e.g. DTPA, into HLLW without any effects on the MA(III) adsorption.

  2. Supported liquid membranes

    SciTech Connect

    Danesi, P.R.

    1984-01-01

    The possibility of utilizing thin layers of organic solutions of solvent extraction reagents, immobilized on microporous inert supports interposed between two aqueous solutions, for selectively removing metal ions from a mixture represents an attractive alternative to liquid-liquid extraction. A detailed knowledge of the liquid-liquid extraction equilibria and mass transfer kinetics is required to understand and to describe quantitatively the rate laws which control the permeation of metal species through Supported Liquid Membranes (SLM) and to exploit them for separation processes. This paper attempts to understand the mechanism of transport through SLM.

  3. Role of the deposition temperature on the self-assembly of the non-planar molecule benzene-1,3,5-triphosphonic acid (BTP) at the liquid-solid interface.

    PubMed

    Nguyen, Doan Chau Yen; Smykalla, Lars; Nguyen, Thi Ngoc Ha; Mehring, Michael; Hietschold, Michael

    2016-09-21

    Benzene-1,3,5-triphosphonic acid (BTP) contains three non-planar phosphonic acid groups which enable three-dimensional hydrogen bonding. Because of these versatile 3D functional groups, BTP is an interesting intermediate to design both 2D and 3D supramolecular hydrogen-bonded architectures and organic-inorganic hybrid frameworks. However, the adsorption of BTP has surprisingly not been the subject of scanning tunneling microscopy (STM) investigations so far. Here a STM study of the adsorption pattern of BTP as obtained from deposition out of a solution in undecanol on an interface to highly-oriented pyrolytic graphite (HOPG) is presented. Furthermore, the influence of the substrate temperature during the deposition from solution on the self-assembly is investigated. High-resolution STM images reveal that the BTB molecules usually form various structures by co-adsorption with undecanol and that the BTP molecules as parts of self-assembled aggregates adsorb with their benzene ring planes tilted with respect to the substrate plane. The specific supramolecular pattern and the 2D packing density of BTP can be precisely tuned by adjusting the initial substrate temperature during deposition. The experimental results are compared to corresponding model structures obtained from semi-empirical simulations and explained by the influence of temperature on the concentration at the solution-solid interface and the kinetics of the self-assembly process. Based on these results, the control of the deposition substrate temperature has been proven to be a versatile tool to control the polymorphism of molecular patterns deposited out of solutions. PMID:27530556

  4. Supported liquid membrane electrochemical separators

    SciTech Connect

    Pemsler, J. Paul; Dempsey, Michael D.

    1986-01-01

    Supported liquid membrane separators improve the flexibility, efficiency and service life of electrochemical cells for a variety of applications. In the field of electrochemical storage, an alkaline secondary battery with improved service life is described in which a supported liquid membrane is interposed between the positive and negative electrodes. The supported liquid membranes of this invention can be used in energy production and storage systems, electrosynthesis systems, and in systems for the electrowinning and electrorefining of metals.

  5. Method of fabrication of supported liquid membranes

    SciTech Connect

    Luebke, David R.; Hong, Lei; Myers, Christina R.

    2015-11-17

    Method for the fabrication of a supported liquid membrane having a dense layer in contact with a porous layer, and a membrane liquid layer within the interconnected pores of the porous layer. The dense layer is comprised of a solidified material having an average pore size less than or equal to about 0.1 nanometer, while the porous layer is comprised of a plurality of interconnected pores and has an average pore size greater than 10 nanometers. The supported liquid membrane is fabricated through the preparation of a casting solution of a membrane liquid and a volatile solvent. A pressure difference is established across the dense layer and porous layer, the casting solution is applied to the porous layer, and the low viscosity casting solution is drawn toward the dense layer. The volatile solvent is evaporated and the membrane liquid precipitates, generating a membrane liquid layer in close proximity to the dense layer.

  6. Phenol removal by supported liquid membranes

    SciTech Connect

    Zha, F.F.; Fane, A.G.; Fell, C.J.D.

    1994-11-01

    This paper examines the application of the supported liquid membrane (SLM) to phenol removal. n-Decanol was proven to be a suitable membrane liquid. The phenol transfer kinetics through the SLMs is quantitatively estimated according to models based on the resistance-in-series concept. The models can be modified to describe the performance of decayed SLMs and thereby provide insight into the effect of membrane liquid loss and penetration of aqueous solutions on the phenol flux. An experimental method is described for the measurement of mass transfer coefficients in the bulk phases using the well-characterized Anopore membrane.

  7. Separation of metals by supported liquid membranes

    SciTech Connect

    Takigawa, D.Y.

    1990-12-31

    A supported liquid membrane system for the separation of a preselected chemical species within a feedstream, preferably an aqueous feedstream, includes a feed compartment containing a feed solution having at least one preselected chemical species therein, a stripping compartment containing a stripping solution therein, and a microporous polybenzimidazole membrane situated between the compartments, the microporous polybenzimidazole membrane containing an extractant mixture selective for the preselected chemical species within the membrane pores is disclosed along with a method of separating preselected chemical species from a feedstream with such a system, and a supported liquid membrane for use in such a system.

  8. Separation of metals by supported liquid membrane

    DOEpatents

    Takigawa, Doreen Y.

    1992-01-01

    A supported liquid membrane system for the separation of a preselected chemical species within a feedstream, preferably an aqueous feedstream, includes a feed compartment containing a feed solution having at least one preselected chemical species therein, a stripping compartment containing a stripping solution therein, and a microporous polybenzimidazole membrane situated between the compartments, the microporous polybenzimidazole membrane containing an extractant mixture selective for the preselected chemical species within the membrane pores is disclosed along with a method of separating preselected chemical species from a feedstream with such a system, and a supported liquid membrane for use in such a system.

  9. Flexible Support Liquid Argon Heat Intercept

    SciTech Connect

    Rudland, D.L.; /Fermilab

    1987-05-18

    A device in the flexible support system for the Central Calorimeter is the Liquid Argon Heat Intercept. The purpose of this apparatus is to intercept heat outside the inner vessel so that bubbles do not form inside. If bubbles did happen to form inside the vessel, they would cause an electric arc between the read-out board and the absorption plates, thus destroying the pre-amplifier. Since this heat intercept is located in the center of the flexible support, it must also support the load of the Central Caloimeter. Figure 1 shows how the intercept works. The subcooled liquid argon is driven through a 1/4-inch x 0.049-inch w tube by hydrostatic pressure. the ambient heat boils the subcooled argon. The gaseous argon flows through the tube and is condensed at the top of the vessel by a 100 kW cooling coil. This process is rpesent in all four flexible support systems.

  10. Separations by supported liquid membrane cascades

    DOEpatents

    Danesi, Pier R.

    1986-01-01

    The invention describes a new separation technique which leads to multi-stage operations by the use of a series (a cascade) of alternated carrier-containing supported-liquid membranes. The membranes contain alternatively a liquid cation exchanger extractant and a liquid anion exchanger extractant (or a neutral extractant) as carrier. The membranes are spaced between alternated aqueous electrolytic solutions of different composition which alternatively provide positively charged extractable species and negatively charged (or zero charged) extractable species, of the chemical species to be separated. The alternated aqueous electrolytic solutions in addition to providing the driving force to the process, simultaneously function as a stripping solution from one type of membrane and as an extraction-promoting solution for the other type of membrane. The aqueous electrolytic solutions and the supported liquid membranes are arranged in such a way to provide a continuous process which leads to the continuous enrichment of the species which show the highest permeability coefficients. By virtue of the very high number of stages which can be arranged, even chemical species having very similar chemical behavior (and consequently very similar permeability coefficients) can be completely separated. The invention also provide a way to concentrate the separated species.

  11. A remarkable enhancement in Am³⁺/Eu³⁺ selectivity by an ionic liquid based solvent containing bis-1,2,4-triazinyl pyridine derivatives: DFT validation of experimental results.

    PubMed

    Bhattacharyya, Arunasis; Ansari, Seraj A; Gadly, Trilochan; Ghosh, Sunil K; Mohapatra, Manoj; Mohapatra, P K

    2015-04-01

    Mutual separation of trivalent actinide (An(3+)) and lanthanide (Ln(3+)) using several soft (N) donor ligands (bis(5,6-dialkyl-1,2,4-triazinyl)pyridine (R-BTP)) is attempted for the first time in room temperature ionic liquid (RTIL) medium. The results indicate a spectacular enhancement in the selectivity as compared to that in molecular diluents with a separation factor (S.F.) of >3000 for Am(3+) over Eu(3+) using the methyl derivative (Me-BTP) in RTIL medium using [C(n)mim]·[NTf2] as the diluents (where n = 2, 3, 4, 6 or 8). Such a high S.F. value has never been reported before with any of the R-BTP derivatives in molecular diluents. An opposite trend in the distribution ratio values of both Am(3+) and Eu(3+) with the increasing size of the alkyl (R) group is observed in RTIL medium when compared with that in molecular diluents. The differences in the extraction behaviour of R-BTPs in RTILs vis-à-vis molecular diluents are explained on the basis of the difference in the nature of complexes extracted in these two distinctly different media as supported by the time resolved fluorescence (TRFS) study. An unusually high extractability and selectivity for Am(3+) over Eu(3+) with Me-BTP was attributed to the formation of a 1 : 4 complex for Am(3+), which was never reported earlier with any of the R-BTP derivatives in molecular diluents. DFT studies indicated higher metal 'd' and 'f' orbital participation (covalence) in the bonding with R-BTP in the case of Am(3+) complexes as compared to that in the case of Eu(3+) complexes, which resulted in the selectivity of these classes of ligands. The observed results may have a great significance in the radioactive waste management involving the partitioning and transmutation strategy. PMID:25736729

  12. Radiolysis and Ageing of C2-BTP in Cinnamaldehyde/Hexanol Mixtures

    SciTech Connect

    Fermvik, Anna; Ekberg, Christian; Retegan, Teodora; Skarnemark, Gunnar

    2007-07-01

    The separation of actinides from lanthanides is an important step in the alternative methods for nuclear waste treatment currently under development. Polycyclic molecules containing nitrogen are synthesised and used for solvent extraction. A potential problem in the separation process is the degradation of the molecule due to irradiation or ageing. An addition of nitrobenzene has proved to have an inhibitory effect on degradation when added to a system containing C2-BTP in hexanol before irradiation. In this study, 2,6-di(5,6-diethyl-1,2,4-triazine-3-yl)pyridine (C2-BTP) was dissolved in different mixtures of cinnamaldehyde and hexanol and the effects on extraction after ageing and irradiation were investigated. Similar to nitrobenzene, cinnamaldehyde contains an aromatic ring which generally has a relatively high resistance towards radiolysis. Both C2-BTP in cinnamaldehyde and C2-BTP in hexanol seem to degrade with time. The system with C2-BTP in pure hexanol is relatively stable up to 17 days but then starts slowly to degrade. The solution with pure cinnamaldehyde as diluent started to degrade after only {approx}20 hours. The opposite is true for degradation caused by radiolysis; hexanol systems are more sensitive to radiolysis than cinnamaldehyde systems. Most of the radiolytic degradation took place during the first days of irradiation, up to a dose of 4 kGy. (authors)

  13. Supported liquid membrane battery separators. Final report

    SciTech Connect

    Pemsler, J.P.; Dempsey, M.D.

    1984-07-01

    This study was performed to explore the feasibility of using a supported liquid membrane (SLM) as a separator in the nickel-zinc battery. In particular, SLM separators should prevent zinc dendrite growth from shorting out the cell and might also alleviate capacity loss due to zinc electrode shape changes. A number of ion exchange/solvent modifier systems for incorporation into SLMs were developed under a previous LBL contract. SLMs prepared with these reagents exhibited resistances in the range of 0.4 to 10 ohm cm/sup 2/, selectively transported hydroxyl ions over zincate ions by a factor of 10/sup 6/ to 10/sup 7/, and possessed eletrochemical and chemical stability in alkaline electrolytes. In order to evaluate these SLM separators under conditions closely resembling a commercial Ni-Zn cell, an accelerated cycle life test was devised using commercial electrodes.

  14. Immunologic trapping in supported liquid membrane extraction

    PubMed

    Thordarson; Jonsson; Emneus

    2000-11-01

    To obtain a high degree of selectivity in sample preparation, supported liquid membrane (SLM) extraction was combined with immunologic recognition. The SLM employs a hydrophobic polymer for supporting the immobilization of an organic solvent, thus forming a nonporous membrane. Said membrane separates the aqueous sample on one side (donor) from a receiving aqueous phase on the other (acceptor). The extraction involves the partitioning of neutral compounds between the sample solution, continuously pumped alongside the membrane, and the membrane. From the membrane, reextraction takes place into a second aqueous phase containing antibodies specific for the target compound(s). Hence, there is a formation of an antibody-antigen complex at the heart of the sample preparation (ImmunoSLM). When the immunocomplex forms, the antigen can no longer redissolve in the organic membrane, thus being trapped in the acceptor. Consequently, the concentration gradient of free antigen over the membrane is ideally unaffected, this being the driving force for the process. With a surplus of antibody, the concentration of analyte in the receiving phase will easily exceed the initial sample concentration. In this work, the so formed immunocomplex was quantified on-line, using a fluorescein flow immunoassay in a sequential injection analysis (SIA) setup. The outlined ImmunoSLM-SIA scheme was successfully applied for the extraction of 4-nitrophenol from spiked water solutions as well as from a spiked wastewater sample, indicating that the immunoextraction can be suitable when dealing with difficult matrixes. PMID:11080876

  15. Development of Practical Supported Ionic Liquid Membranes: A Systematic Approach

    SciTech Connect

    Luebke, D.R.; Ilconich, J.B.; Myers, C.R.; Pennline, H.W.

    2007-11-01

    Supported liquid membranes (SLMs) are a class of materials that allow the researcher to utilize the wealth of knowledge available on liquid properties to optimize membrane performance. These membranes also have the advantage of liquid phase diffusivities, which are higher than those observed in polymers and grant proportionally greater permeabilities. The primary shortcoming of the supported liquid membranes demonstrated in past research has been the lack of stability caused by volatilization of the transport liquid. Ionic liquids, which may possess high CO2 solubility relative to light gases such as H2, are excellent candidates for this type of membrane since they are stable at elevated temperatures and have negligible vapor pressure. A study has been conducted evaluating the use of a variety of ionic liquids in supported ionic liquid membranes for the capture of CO2 from streams containing H2. In a joint project, researchers at the University of Notre Dame synthesized and characterized ionic liquids, and researchers at the National Energy Technology Laboratory incorporated candidate ionic liquids into supports and evaluated membrane performance for the resulting materials. Several steps have been taken in the development of practical supported ionic liquid membranes. Proof-of-concept was established by showing that ionic liquids could be used as the transport media in SLMs. Results showed that ionic liquids are suitable media for gas transport, but the preferred polymeric supports were not stable at temperatures above 135oC. The use of cross-linked nylon66 supports was found to produce membranes mechanically stable at temperatures exceeding 300oC but CO2/H2 selectivity was poor. An ionic liquid whose selectivity does not decrease with increasing temperature was needed, and a functionalized ionic liquid that complexes with CO2 was used. An increase in CO2/H2 selectivity with increasing temperature over the range of 37 to 85oC was observed and the dominance of a

  16. Carbon Dioxide Separation with Supported Ionic Liquid Membranes

    SciTech Connect

    Luebke, D.R.; Ilconich, J.B.; Myers, C.R.; Pennline, H.W.

    2007-04-01

    Supported liquid membranes are a class of materials that allow the researcher to utilize the wealth of knowledge available on liquid properties as a direct guide in the development of a capture technology. These membranes also have the advantage of liquid phase diffusivities higher than those observed in polymeric membranes which grant proportionally greater permeabilities. The primary shortcoming of the supported liquid membranes demonstrated in past research has been the lack of stability caused by volatilization of the transport liquid. Ionic liquids, which possess high carbon dioxide solubility relative to light gases such as hydrogen, are an excellent candidate for this type of membrane since they have negligible vapor pressure and are not susceptible to evaporation. A study has been conducted evaluating the use of several ionic liquids, including 1-hexyl-3-methyl-imidazolium bis(trifuoromethylsulfonyl)imide, 1-butyl-3-methyl-imidazolium nitrate, and 1-ethyl-3-methyl-imidazolium sulfate in supported ionic liquid membranes for the capture of carbon dioxide from streams containing hydrogen. In a joint project, researchers at the University of Notre Dame lent expertise in ionic liquid synthesis and characterization, and researchers at the National Energy Technology Laboratory incorporated candidate ionic liquids into supports and evaluated the resulting materials for membrane performance. Initial results have been very promising with carbon dioxide permeabilities as high as 950 barrers and significant improvements in carbon dioxide/hydrogen selectivity over conventional polymers at 37C and at elevated temperatures. Results include a comparison of the performance of several ionic liquids and a number of supports as well as a discussion of innovative fabrication techniques currently under development.

  17. 26. DETAIL OF CONCRETE PIPE SUPPORTS LEADING TO NEW LIQUID ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    26. DETAIL OF CONCRETE PIPE SUPPORTS LEADING TO NEW LIQUID HYDROGEN TANK FARM; VIEW TO WEST. - Cape Canaveral Air Station, Launch Complex 17, Facility 28402, East end of Lighthouse Road, Cape Canaveral, Brevard County, FL

  18. Fabrication of fiber supported ionic liquids and methods of use

    SciTech Connect

    Luebke, David R; Wickramanayake, Shan

    2013-02-26

    One or more embodiments relates to the production of a fabricated fiber having an asymmetric polymer network and having an immobilized liquid such as an ionic liquid within the pores of the polymer network. The process produces the fabricated fiber in a dry-wet spinning process using a homogenous dope solution, providing significant advantage over current fabrication methods for liquid-supporting polymers. The fabricated fibers may be effectively utilized for the separation of a chemical species from a mixture based on the selection of the polymer, the liquid, and the solvent utilized in the dope.

  19. Failure Mechanisms of Hollow Fiber Supported Ionic Liquid Membranes

    PubMed Central

    Zeh, Matthew; Wickramanayake, Shan; Hopkinson, David

    2016-01-01

    Hollow fiber supported ionic liquid membranes (SILMs) were tested using the bubble point method to investigate potential failure modes, including the maximum transmembrane pressure before loss of the ionic liquid from the support. Porous hollow fiber supports were fabricated with different pore morphologies using Matrimid® and Torlon® as the polymeric material and 1-hexyl-3-methylimidalzolium bis(trifluoromethylsulfonyl)imide ([C6mim][Tf2N]) as the ionic liquid (IL) component. Hollow fiber SILMs were tested for their maximum pressure before failure, with pressure applied either from the bore side or shell side. It was found that the membranes exhibited one or more of three different modes of failure when pressurized: liquid loss (occurring at the bubble point), rupture, and collapse. PMID:27023620

  20. Rejuvenation of Spent Media via Supported Emulsion Liquid Membranes

    NASA Technical Reports Server (NTRS)

    Wiencek, John M.

    2002-01-01

    The overall goal of this project was to maximize the reuseability of spent fermentation media. Supported emulsion liquid membrane separation, a highly efficient extraction technique, was used to remove inhibitory byproducts during fermentation; thus, improve the yield while reducing the need for fresh water. The key objectives of this study were: (1) Develop an emulsion liquid membrane system targeting low molecular weight organic acids which has minimal toxicity on a variety of microbial systems. (2) Conduct mass transfer studies to allow proper modeling and design of a supported emulsion liquid membrane system. (3) Investigate the effect of gravity on emulsion coalescence within the membrane unit. (4) Access the effect of water re-use on fermentation yields in a model microbial system. and (5) Develop a perfusion-type fermentor utilizing a supported emulsion liquid membrane system to control inhibitory fermentation byproducts (not completed due to lack of funds)

  1. Failure Mechanisms of Hollow Fiber Supported Ionic Liquid Membranes.

    PubMed

    Zeh, Matthew; Wickramanayake, Shan; Hopkinson, David

    2016-01-01

    Hollow fiber supported ionic liquid membranes (SILMs) were tested using the bubble point method to investigate potential failure modes, including the maximum transmembrane pressure before loss of the ionic liquid from the support. Porous hollow fiber supports were fabricated with different pore morphologies using Matrimid(®) and Torlon(®) as the polymeric material and 1-hexyl-3-methylimidalzolium bis(trifluoromethylsulfonyl)imide ([C₆mim][Tf₂N]) as the ionic liquid (IL) component. Hollow fiber SILMs were tested for their maximum pressure before failure, with pressure applied either from the bore side or shell side. It was found that the membranes exhibited one or more of three different modes of failure when pressurized: liquid loss (occurring at the bubble point), rupture, and collapse. PMID:27023620

  2. A BTP1 prophage gene present in invasive non-typhoidal Salmonella determines composition and length of the O-antigen of the lipopolysaccharide.

    PubMed

    Kintz, Erica; Davies, Mark R; Hammarlöf, Disa L; Canals, Rocío; Hinton, Jay C D; van der Woude, Marjan W

    2015-04-01

    Salmonella Typhimurium isolate D23580 represents a recently identified ST313 lineage of invasive non-typhoidal Salmonellae (iNTS). One of the differences between this lineage and other non-iNTS S. Typhimurium isolates is the presence of prophage BTP1. This prophage encodes a gtrC gene, implicated in O-antigen modification. GtrC(BTP) (1) is essential for maintaining O-antigen length in isolate D23580, since a gtr(BTP) (1) mutant yields a short O-antigen. This phenotype can be complemented by gtrC(BTP) (1) or very closely related gtrC genes. The short O-antigen of the gtr(BTP) (1) mutant was also compensated by deletion of the BTP1 phage tailspike gene in the D23580 chromosome. This tailspike protein has a putative endorhamnosidase domain and thus may mediate O-antigen cleavage. Expression of the gtrC(BTP) (1) gene is, in contrast to expression of many other gtr operons, not subject to phase variation and transcriptional analysis suggests that gtrC is produced under a variety of conditions. Additionally, GtrC(BTP) (1) expression is necessary and sufficient to provide protection against BTP1 phage infection of an otherwise susceptible strain. These data are consistent with a model in which GtrC(BTP) (1) mediates modification of the BTP1 phage O-antigen receptor in lysogenic D23580, and thereby prevents superinfection by itself and other phage that uses the same O-antigen co-receptor. PMID:25586744

  3. Alkaline ionic liquids applied in supported ionic liquid catalyst for selective hydrogenation of citral to citronellal

    NASA Astrophysics Data System (ADS)

    Salminen, Eero; Virtanen, Pasi; Mikkola, Jyri-Pekka

    2014-02-01

    The challenge in preparation of ionic liquids containing a strong alkaline anion is to identify a suitable cation which can tolerate the harsh conditions induced by the anion. In this study, a commercial quaternary ammonium compound (quat) benzalkonium [ADBA] (alkyldimethylbenzylammonium) was used as a cation in the synthesis of different alkaline ionic liquids. In fact, the precursor, benzalkonium chloride, is a mixture of alkyldimethylbenzylammonium chlorides of various alkyl chain lengths and is commonly used in the formulation of various antiseptic products. The prepared ionic liquids were utilized as Supported Ionic Liquid Catalysts (SILCAs). Typically, a SILCA contains metal nanoparticles, enzymes or metal complexes in an ionic liquid layer which is immobilized on a solid carrier material such as an active carbon cloth (ACC). The catalysts were applied in the selective hydrogenation of citral to citronellal which is an important perfumery chemical. Interestingly, 70 % molar yield towards citronellal was achieved over a catalyst containing the alkaline ionic liquid benzalkonium methoxide.

  4. Alkaline ionic liquids applied in supported ionic liquid catalyst for selective hydrogenation of citral to citronellal.

    PubMed

    Salminen, Eero; Virtanen, Pasi; Mikkola, Jyri-Pekka

    2014-01-01

    The challenge in preparation of ionic liquids containing a strong alkaline anion is to identify a suitable cation which can tolerate the harsh conditions induced by the anion. In this study, a commercial quaternary ammonium compound (quat) benzalkonium [ADBA] (alkyldimethylbenzylammonium) was used as a cation in the synthesis of different alkaline ionic liquids. In fact, the precursor, benzalkonium chloride, is a mixture of alkyldimethylbenzylammonium chlorides of various alkyl chain lengths and is commonly used in the formulation of various antiseptic products. The prepared ionic liquids were utilized as Supported Ionic Liquid Catalysts (SILCAs). Typically, a SILCA contains metal nanoparticles, enzymes, or metal complexes in an ionic liquid layer which is immobilized on a solid carrier material such as an active carbon cloth (ACC). The catalysts were applied in the selective hydrogenation of citral to citronellal which is an important perfumery chemical. Interestingly, 70% molar yield toward citronellal was achieved over a catalyst containing the alkaline ionic liquid benzalkonium methoxide. PMID:24790972

  5. Alkaline ionic liquids applied in supported ionic liquid catalyst for selective hydrogenation of citral to citronellal

    PubMed Central

    Salminen, Eero; Virtanen, Pasi; Mikkola, Jyri-Pekka

    2014-01-01

    The challenge in preparation of ionic liquids containing a strong alkaline anion is to identify a suitable cation which can tolerate the harsh conditions induced by the anion. In this study, a commercial quaternary ammonium compound (quat) benzalkonium [ADBA] (alkyldimethylbenzylammonium) was used as a cation in the synthesis of different alkaline ionic liquids. In fact, the precursor, benzalkonium chloride, is a mixture of alkyldimethylbenzylammonium chlorides of various alkyl chain lengths and is commonly used in the formulation of various antiseptic products. The prepared ionic liquids were utilized as Supported Ionic Liquid Catalysts (SILCAs). Typically, a SILCA contains metal nanoparticles, enzymes, or metal complexes in an ionic liquid layer which is immobilized on a solid carrier material such as an active carbon cloth (ACC). The catalysts were applied in the selective hydrogenation of citral to citronellal which is an important perfumery chemical. Interestingly, 70% molar yield toward citronellal was achieved over a catalyst containing the alkaline ionic liquid benzalkonium methoxide. PMID:24790972

  6. Rejuvenation of Spent Media via Supported Emulsion Liquid Membranes

    NASA Technical Reports Server (NTRS)

    Wiencek, John M.

    2002-01-01

    The overall goal of this project is to maximize the reuseability of spent fermentation media. Supported emulsion liquid membrane separation, a highly efficient extraction technique, is used to remove inhibitory byproducts during fermentation; thus, improving the yield while reducing the need for fresh water. The key objectives of this study are: Develop an emulsion liquid membrane system targeting low molecular weight organic acids which has minimal toxicity on a variety of microbial systems; Conduct mass transfer studies to allow proper modeling and design of a supported emulsion liquid membrane system; Investigate the effect of gravity on emulsion coalescence within the membrane unit; Access the effect of water re-use on fermentation yields in a model microbial system; Develop a perfusion-type fermentor utilizing a supported emulsion liquid membrane system to control inhibitory fermentation byproducts; Work for the coming year will focus on the determination of toxicity of various solvents, selection of the emulsifying agents, as well as characterizing the mass transfer of hollow-fiber contactors.

  7. Liquid-Mercury-Supported Langmuir Films of Ionic Liquids: Isotherms, Structure, and Time Evolution.

    PubMed

    Elfassy, Eitan; Mastai, Yitzhak; Pontoni, Diego; Deutsch, Moshe

    2016-04-01

    Ionic liquids have been intensively developed for the last few decades and are now used in a wide range of applications, from electrochemistry to catalysis and nanotechnology. Many of these applications involve ionic liquid interfaces with other liquids and solids, the subnanometric experimental study of which is highly demanding, and has been little studied to date. We present here a study of mercury-supported Langmuir films of imidazolium-based ionic liquids by surface tensiometry and X-ray reflectivity. The charge-delocalized ionic liquids studied here exhibit no 2D lateral order but show diffuse surface-normal electron density profiles exhibiting gradual mercury penetration into the ionic liquid film, and surface-normal structure evolution over a period of hours. The effect of increasing the nonpolar alkyl chain length was also investigated. The results obtained provide insights into the interactions between these ionic liquids and liquid mercury and about the time evolution of the structure and composition of their interface. PMID:26963651

  8. Supported liquid inorganic membranes for nuclear waste separation

    SciTech Connect

    Bhave, Ramesh R; DeBusk, Melanie M; DelCul, Guillermo D; Delmau, Laetitia H; Narula, Chaitanya K

    2015-04-07

    A system and method for the extraction of americium from radioactive waste solutions. The method includes the transfer of highly oxidized americium from an acidic aqueous feed solution through an immobilized liquid membrane to an organic receiving solvent, for example tributyl phosphate. The immobilized liquid membrane includes porous support and separating layers loaded with tributyl phosphate. The extracted solution is subsequently stripped of americium and recycled at the immobilized liquid membrane as neat tributyl phosphate for the continuous extraction of americium. The sequestered americium can be used as a nuclear fuel, a nuclear fuel component or a radiation source, and the remaining constituent elements in the aqueous feed solution can be stored in glassified waste forms substantially free of americium.

  9. A TRLFS study on the complexation of novel BTP type ligands with Cm(III).

    PubMed

    Beele, Björn B; Rüdiger, Elias; Schwörer, Felicitas; Müllich, Udo; Geist, Andreas; Panak, Petra J

    2013-09-14

    Two BTP-type N-donor ligands with different numbers of aromatic nitrogen atoms (2,6-bis(4-ethyl-pyridazin-1-yl)pyridine, Et-BDP and 2,6-bis(4-(n)propyl-2,3,5,6-tetrazine-1-yl)pyridine, (n)Pr-Tetrazine) have been synthesized and characterized by NMR and MS techniques. The complexation with Cm(III) in 2-propanol-water (1 : 1, vol.) is studied for both ligands using time resolved laser-induced fluorescence spectroscopy (TRLFS) and the complexation properties are compared to (n)Pr-BTP. With increasing the ligand concentration three different species, the 1 : 1-, 1 : 2- and 1 : 3-complex, were found. Log β3 values of 7.6 for the formation of Cm(Et-BDP)3 and 9.2 for the formation of Cm((n)Pr-Tetrazine)3 are determined. The complexation with (n)Pr-Tetrazine shows slow kinetics. Thermodynamic data of the complexation reactions are determined in a temperature range of 25 °C-60 °C. The complexation with Et-BDP is exothermic (ΔH = -16.3 ± 1.2 kJ mol(-1)) and exergonic (ΔG = -43.8 ± 2.6 kJ mol(-1)) whereas the complexation with (n)Pr-Tetrazine is endothermic (ΔH = 43.9 ± 3.1 kJ mol(-1)) and exergonic (ΔG = -51.7 ± 2.2 kJ mol(-1)). In the case of the latter the complexation is driven by a highly positive reaction entropy change (ΔS = 320.6 ± 15.4 J mol(-1) K(-1)). In comparison to (n)Pr-BTP, less negative ΔG values were found for the complexation of Cm(III) with both ligands. PMID:23552476

  10. Feasibility of Surfactant-Free Supported Emulsion Liquid Membrane Extraction

    NASA Technical Reports Server (NTRS)

    Hu, Shih-Yao B.; Li, Jin; Wiencek, John M.

    2001-01-01

    Supported emulsion liquid membrane (SELM) is an effective means to conduct liquid-liquid extraction. SELM extraction is particularly attractive for separation tasks in the microgravity environment where density difference between the solvent and the internal phase of the emulsion is inconsequential and a stable dispersion can be maintained without surfactant. In this research, dispersed two-phase flow in SELM extraction is modeled using the Lagrangian method. The results show that SELM extraction process in the microgravity environment can be simulated on earth by matching the density of the solvent and the stripping phase. Feasibility of surfactant-free SELM (SFSELM) extraction is assessed by studying the coalescence behavior of the internal phase in the absence of the surfactant. Although the contacting area between the solvent and the internal phase in SFSELM extraction is significantly less than the area provided by regular emulsion due to drop coalescence, it is comparable to the area provided by a typical hollow-fiber membrane. Thus, the stripping process is highly unlikely to become the rate-limiting step in SFSELM extraction. SFSELM remains an effective way to achieve simultaneous extraction and stripping and is able to eliminate the equilibrium limitation in the typical solvent extraction processes. The SFSELM design is similar to the supported liquid membrane design in some aspects.

  11. Wind and seismic analysis for liquid-level gauge support

    SciTech Connect

    Ziada, A.H.

    1994-12-07

    A wind and seismic analysis was performed for the liquid-level gauge installation support stand. The analysis includes the stand and footing only. All of these supports are classified as safety class 3. The analysis was based on safety class 2 requirements for conservatism. Conventional hand calculations were performed to evaluate the stresses and overturning of the structure. The results and recommendations appear in Section 2.0. The configuration and loadings are discussed in Section 3.0; the analysis and evaluation appears in Section 4.0; and the detailed analysis is documented in Appendix A.

  12. Cooling tower with concrete support structure, fiberglass panels, and a fan supported by the liquid distribution system

    SciTech Connect

    Bardo, C. J.; Clark Jr., J. L.; Dylewski, A. J.; Seawell, J. Q.

    1985-09-24

    A liquid cooling tower includes precast concrete support legs and cross beams and fiberglass reinforced polyester resin side and top panels. A liquid distribution system is supplied with liquid by a vertically extending main pipe, and a fan and fan motor are supported by the main pipe.

  13. Ionic liquids in refinery desulfurization: comparison between biphasic and supported ionic liquid phase suspension processes.

    PubMed

    Kuhlmann, Esther; Haumann, Marco; Jess, Andreas; Seeberger, Andreas; Wasserscheid, Peter

    2009-01-01

    The desulfurization of fuel compounds in the presence of ionic liquids is reported. For this purpose, the desulfurization efficiency of a variety of imidazolium phosphate ionic liquids has been tested. Dibenzothiophene/dodecane and butylmercaptan/decane mixtures were used as model systems. Single-stage extractions reduced the sulfur content from 500 ppm to 200 ppm. In multistage extractions the sulfur content could be lowered to less than 10 ppm within seven stages. Regeneration of the ionic liquid was achieved by distillation or re-extraction procedures. Supported ionic liquid phase (SILP) materials, obtained by dispersing the ionic liquid as a thin film on highly porous silica, exhibited a significantly higher extraction performance owing to their larger surface areas, reducing the sulfur content to less than 100 ppm in one stage. Multistage extraction with these SILP materials reduced the sulfur level to 50 ppm in the second stage. The SILP technology offers very efficient utilization of ionic liquids and circumvents mass transport limitations because of the small film thickness and large surface area, and allows application of the simple packed-bed column extraction technique. PMID:19798713

  14. A functional link between store-operated and TRPC channels revealed by the 3,5-bis(trifluoromethyl)pyrazole derivative, BTP2.

    PubMed

    He, Li-Ping; Hewavitharana, Thamara; Soboloff, Jonathan; Spassova, Maria A; Gill, Donald L

    2005-03-25

    The coupling between receptor-mediated Ca2+ store release and the activation of "store-operated" Ca2+ entry channels is an important but so far poorly understood mechanism. The transient receptor potential (TRP) superfamily of channels contains several members that may serve the function of store-operated channels (SOCs). The 3,5-bis(trifluoromethyl)pyrazole derivative, BTP2, is a recently described inhibitor of SOC activity in T-lymphocytes. We compared its action on SOC activation in a number of cell types and evaluated its modification of three specific TRP channels, canonical transient receptor potential 3 (TRPC3), TRPC5, and TRPV6, to throw light on any link between SOC and TRP channel function. Using HEK293 cells, DT40 B cells, and A7r5 smooth muscle cells, BTP2 blocked store-operated Ca2+ entry within 10 min with an IC50 of 0.1-0.3 microM. Store-operated Ca2+ entry induced by Ca2+ pump blockade or in response to muscarinic or B cell receptor activation was similarly sensitive to BTP2. Using the T3-65 clonal HEK293 cell line stably expressing TRPC3 channels, TRPC3-mediated Sr2+ entry activated by muscarinic receptors was also blocked by BTP2 with an IC50 of <0.3 microM. Importantly, direct activation of TRPC3 channels by diacylglycerol was also blocked by BTP2 (IC50 approximately 0.3 microM). BTP2 still blocked TRPC3 in medium with N-methyl-D-glucamine-chloride replacing Na+, indicating BTP2 did not block divalent cation entry by depolarization induced by activating monovalent cation entry channels. Whereas whole-cell carbachol-induced TRPC3 current was blocked by 3 microM BTP2, single TRPC3 channel recordings revealed persistent short openings suggesting BTP2 reduces the open probability of the channel rather than its pore properties. TRPC5 channels transiently expressed in HEK293 cells were blocked by BTP2 in the same range as TRPC3. However, function of the highly Ca(2+)-selective TRPV6 channel, with many channel properties akin to SOCs, was entirely

  15. Systemic resistance and lipoxygenase-related defence response induced in tomato by Pseudomonas putida strain BTP1

    PubMed Central

    Akram, Adam; Ongena, Marc; Duby, Francéline; Dommes, Jacques; Thonart, Philippe

    2008-01-01

    Background Previous studies showed the ability of Pseudomonas putida strain BTP1 to promote induced systemic resistance (ISR) in different host plants. Since ISR is long-lasting and not conducive for development of resistance of the targeted pathogen, this phenomenon can take part of disease control strategies. However, in spite of the numerous examples of ISR induced by PGPR in plants, only a few biochemical studies have associated the protective effect with specific host metabolic changes. Results In this study, we showed the protective effect of this bacterium in tomato against Botrytis cinerea. Following treatment by P. putida BTP1, analyses of acid-hydrolyzed leaf extracts showed an accumulation of antifungal material after pathogen infection. The fungitoxic compounds thus mainly accumulate as conjugates from which active aglycones may be liberated through the activity of hydrolytic enzymes. These results suggest that strain BTP1 can elicit systemic phytoalexin accumulation in tomato as one defence mechanism. On another hand, we have shown that key enzymes of the lipoxygenase pathway are stimulated in plants treated with the bacteria as compared with control plants. Interestingly, this stimulation is observed only after pathogen challenge in agreement with the priming concept almost invariably associated with the ISR phenomenon. Conclusion Through the demonstration of phytoalexin accumulation and LOX pathway stimulation in tomato, this work provides new insights into the diversity of defence mechanisms that are inducible by non-pathogenic bacteria in the context of ISR. PMID:19000301

  16. Separation of metal species by supported liquid membranes

    SciTech Connect

    Danesi, P.R.

    1985-01-01

    The work performed in the Separation Chemistry Group of the Chemistry Division of Argonne National Laboratory on the transport and separation properties of supported liquid membranes (SLM) are reviewed. The models and equations which describe the permeation through SLMs of metal species are described. These models have been tested with various carriers absorbed on flat-sheet and hollow-fiber SLMs by measuring the permeation of several metal species of hydrometallurgical and nuclear interest. An equation for the separation factor of metal species in SLM processes and examples of separations of metal ions are reported. The possibility of bypassing the single stage character of SLM separations by using multilayer composite SLMs, arranged in series, is also analyzed. Finally, the factors which control the stability of SLMs are briefly discussed. 28 references, 27 figures, 6 tables.

  17. Separation of metal species by supported liquid membranes

    SciTech Connect

    Danesi, P.R.

    1984-01-01

    The works performed on the transport and separation properties of supported liquid membranes (SLM) are reviewed. The models and equations which describe the permeation through SLMs of metal species are described. These models have been tested with various carriers absorbed on flat-sheet and hollow-fiber SLMs by measuring the permeation of several metal species of hydrometallurgical and nuclear interest. An equation for the separation factor of metal species in SLM processes and examples of separations of metal ions are reported. The possibility of bypassing the single stage character of SLM separations by using multilayer composite SLMs, arranged in series, is also analyzed. Finally, the factors which control the stability of SLMs are briefly discussed.

  18. Ionic liquid based hollow fiber supported liquid phase microextraction of ultraviolet filters.

    PubMed

    Ge, Dandan; Lee, Hian Kee

    2012-03-16

    Hollow fiber protected liquid phase microextraction using an ionic liquid as supported phase and acceptor phase (IL-HF-LPME) is proposed for the determination of four ultraviolet (UV) filters (benzophenone, 3-(4-methylbenzylidene)-camphor, 2-hydroxy-4-methoxybenzophenone and 2,4-dihydroxybenzophenone) in water samples for the first time. In the present study, four different ILs 1-hexyl-3-methylimidazolium tris(pentafluoroethyl)trifluorophosphate) [HMIM][FAP], 1-butyl-1-methylpyrrolidinium tris(pentafluoroethyl)trifluorophosphate [BMPL][FAP], 1-butyl-3-methylimidazolium phosphate ([BMIM][PO(4)]) and 1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM][PF(6)]) were evaluated as extraction solvent. Only [HMIM][FAP] showed high chemical affinity to the analytes which permits a selective isolation of the UV filters from the sample matrix, allowing also their preconcentration. IL-HF-LPME and high performance liquid chromatography provides repeatability from 1.1% to 8.2% and limits of detection between 0.3 and 0.5 ng/ml. Real water samples spiked with the analytes extracted were analyzed, and yielded relative recoveries ranging from 82.6% to 105.9%. PMID:22307149

  19. Properties required by extractants and diluents for the decontamination of liquid wastes using supported liquid membranes

    SciTech Connect

    Dozol, J.F.; Rouquette, H.; Eymard, S.; Tournois, B.

    1993-12-31

    Macrocyclic extractants are now being studied more and more often for the decontamination of radioactive liquid wastes: coronands (crown ethers, azacrown...) and cryptands. As these very sophisticated compounds are expensive, the best technique is supported liquid membranes which need a very low extractant inventory. This paper deals with the properties required by the extractant and the diluent in order to be used in an SLM device and to ensure a stable and efficient SLM: solubility of the extractant in organic compounds and in aqueous solutions; size of crown ether cavities; influence of the substituent groups on the selectivity of the crown ether; and influence of the properties of the diluent (polarity, transport of acidity) on the efficiency of the process and on the stability of the membrane (interfacial tension between the organic and aqueous phases, solubility in the aqueous phase). The influence of these parameters is illustrated by experiments performed in order to remove strontium and cesium from high sodium content liquid waste. The studies described in this paper are focused on the decategorization of evaporator concentrates arising from the reprocessing of spent fuel.

  20. The effect of porous support composition and operating parameters on the performance of supported liquid membranes

    SciTech Connect

    Takigawa, D.Y. )

    1992-03-01

    Supported liquid membranes (SLMs) of varying porous support compositions and structures were studied for the transport of metal ions. A microporous polybenzimidazole support was synthesized and prepared in the form of an SLM. This SLM, containing the selective extractant di-(2-ethylhexyl) phosphoric acid, was evaluated for the transport of copper and neodymium. Metal ion transport reaches near completion in less than 3 h, whereas Celgard-polypropylene and Nucleopore-polycarbonate reaches only 50% completion even after 15 h. The transport driving force for acidic extractants is a pH gradient between the feed and strip solutions. Polybenzimidazole, an acid-and radiation-resistant polymer, has two protonatable tertiary nitrogens per repeat unit that may help sustain the pH driving force. Another factor may be the ability of the polybenzimidazole to hydrogen bond with the extractant. Transport through the flat-sheet SLMs was tested by using a unique cell design. Countercurrent flow of the feed and strip solutions was established through machined channels in half-cell face plates that are in a spiral, mirror-image pattern with respect to each other, with the flat-sheet SLM interposed between the two channeled solutions. Advantages comprised in the design of the two clamped half-cells (tangential entry, zero primary pressure, zero pressure differential, controlled flow regimes, no sharp turns, and channeled flow) give operating parameters that will not physically dislodge the liquid membrane from the porous support; consequently, the lifetime of the support is increased. Permeability coefficients remained unchanged after a month of daily use versus 20 to 100% declines for membranes in other cell configurations.

  1. The effect of porous support composition and operating parameters on the performance of supported liquid membranes

    SciTech Connect

    Takigawa, D.Y.

    1991-02-01

    Factors, such as porous support composition and operating parameters, that influence the performance of supported liquid membranes (SLMs) were investigated. SLMs of varying porous support compositions and structures were studied for the transport of metal ions. A microporous polybenzimidazole support was synthesized and prepared in the form of an SLM. This SLM containing the selective extractant di-(2-ethylhexyl)phosphoric acid was evaluated for the transport of copper and neodymium. Dramatically improved performance over that of commercially available membranes was found in tests for removing the metal ions from solution. Metal ion transport reaches near completion in less than 3 hours, whereas Celgard-polypropylene and Nuclepore-polycarbonate reaches only 50% completion even after 15 hours. The transport driving force for acidic extractants is a pH gradient between the feed and strip solutions. Polybenzimidazole, an acid- and radiation-resistant polymer, has two protonatable tertiary nitrogens per repeat unit that may help sustain the pH driving force. Another factor may be the ability of the polybenzimidazole to hydrogen bond with the extractant. Transport through the flat-sheet SLMs were tested using a unique cell design. Countercurrent flow of the feed and strip solutions was established through machined channels in half-cell faceplates that are in a spiral, mirror-image pattern with respect to each other, with the flat-sheet SLM interposed between the two channeled solutions. 7 refs., 14 figs.

  2. Advanced Supported Liquid Membranes for Carbon Dioxide Control in Extravehicular Activity Applications

    NASA Technical Reports Server (NTRS)

    Wickham, David T. (Inventor); Gleason, Kevin J. (Inventor); Cowley, Scott W. (Inventor)

    2015-01-01

    There is disclosed a portable life support system with a component for removal of at least one selected gas. In an embodiment, the system includes a supported liquid membrane having a first side and a second side in opposition to one another, the first side configured for disposition toward an astronaut and the second side configured for disposition toward a vacuum atmosphere. The system further includes an ionic liquid disposed between the first side and the second side of the supported liquid membrane, the ionic liquid configured for removal of at least one selected gas from a region housing the astronaut adjacent the first side of the supported liquid membrane to the vacuum atmosphere adjacent the second side of the supported liquid membrane. Other embodiments are also disclosed.

  3. A BTP1 prophage gene present in invasive non-typhoidal Salmonella determines composition and length of the O-antigen of the lipopolysaccharide

    PubMed Central

    Kintz, Erica; Davies, Mark R; Hammarlöf, Disa L; Canals, Rocío; Hinton, Jay C D; van der Woude, Marjan W

    2015-01-01

    Salmonella Typhimurium isolate D23580 represents a recently identified ST313 lineage of invasive non-typhoidal Salmonellae (iNTS). One of the differences between this lineage and other non-iNTS S. Typhimurium isolates is the presence of prophage BTP1. This prophage encodes a gtrC gene, implicated in O-antigen modification. GtrCBTP1 is essential for maintaining O-antigen length in isolate D23580, since a gtrBTP1 mutant yields a short O-antigen. This phenotype can be complemented by gtrCBTP1 or very closely related gtrC genes. The short O-antigen of the gtrBTP1 mutant was also compensated by deletion of the BTP1 phage tailspike gene in the D23580 chromosome. This tailspike protein has a putative endorhamnosidase domain and thus may mediate O-antigen cleavage. Expression of the gtrCBTP1 gene is, in contrast to expression of many other gtr operons, not subject to phase variation and transcriptional analysis suggests that gtrC is produced under a variety of conditions. Additionally, GtrCBTP1 expression is necessary and sufficient to provide protection against BTP1 phage infection of an otherwise susceptible strain. These data are consistent with a model in which GtrCBTP1 mediates modification of the BTP1 phage O-antigen receptor in lysogenic D23580, and thereby prevents superinfection by itself and other phage that uses the same O-antigen co-receptor. PMID:25586744

  4. Assessing covalency in equatorial U-N bonds: density based measures of bonding in BTP and isoamethyrin complexes of uranyl.

    PubMed

    Di Pietro, Poppy; Kerridge, Andrew

    2016-06-22

    Calculations performed at the density functional level of theory have been used to investigate complexes of uranyl with the expanded porphyrin isoamethyrin and the bis-triazinyl-pyridine (BTP) ligands, the latter of which is well-known to be effective in the separation of trivalent lanthanides and actinides. Analysis has been performed using a range of density-based techniques, including the Quantum Theory of Atoms in Molecules (QTAIM), the Electron Localisation Function (ELF) and the reduced density gradient (RDG). The effects of peripheral alkyl substituents on UO2-isoamethyrin, known to be vital for proper replication of the experimental geometry, are considered. Evidence for comparable amounts of covalent character has been found in the largely ionic U-N bonds of UO2-isoamethyrin and [UO2(BTP)2](2+) and examination of the variation in the electronic characteristics of the uranyl unit upon complexation in both of these cases reveal striking similarities in the nature of the U-N bonding and the effect of this bonding on the U-Oyl interaction, as well as evidence of donation into the U-N bonding region from the uranyl unit itself. PMID:27279271

  5. Early Transcriptional Responses of Bovine Chorioallantoic Membrane Explants to Wild Type, ΔvirB2 or ΔbtpB Brucella abortus Infection

    PubMed Central

    Mol, Juliana P. S.; Costa, Erica A.; Carvalho, Alex F.; Sun, Yao-Hui; Tsolis, Reneé M.; Paixão, Tatiane A.; Santos, Renato L.

    2014-01-01

    The pathogenesis of the Brucella-induced inflammatory response in the bovine placenta is not completely understood. In this study we evaluated the role of the B. abortus Type IV secretion system and the anti-inflammatory factor BtpB in early interactions with bovine placental tissues. Transcription profiles of chorioallantoic membrane (CAM) explants inoculated with wild type (strain 2308), ΔvirB2 or ΔbtpB Brucella abortus were compared by microarray analysis at 4 hours post infection. Transcripts with significant variation (>2 fold change; P<0.05) were functionally classified, and transcripts related to defense and inflammation were assessed by quantitative real time RT-PCR. Infection with wild type B. abortus resulted in slightly more genes with decreased than increased transcription levels. Conversely, infection of trophoblastic cells with the ΔvirB2 or the ΔbtpB mutant strains, that lack a functional T4SS or that has impaired inhibition of TLR signaling, respectively, induced more upregulated than downregulated genes. Wild type Brucella abortus impaired transcription of host genes related to immune response when compared to ΔvirB and ΔbtpB mutants. Our findings suggest that proinflammatory genes are negatively modulated in bovine trophoblastic cells at early stages of infection. The virB operon and btpB are directly or indirectly related to modulation of these host genes. These results shed light on the early interactions between B. abortus and placental tissue that ultimately culminate in inflammatory pathology and abortion. PMID:25259715

  6. Hyperhydricity and flavonoid content of Scutellaria species in vitro on polyester-supported liquid culture systems

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Three Scutellaria species (Scutellaria lateriflora, S. costaricana and S. baicalensis) were grown in different in vitro physical environments: agar, liquid culture, and liquid culture with fiber-supported paper (with initial media volumes of 20 mL and 30 mL). During an eight-week time course, tiss...

  7. SEPARATION PROPERTIES OF SURFACE MODIFIED SILICA SUPPORTED LIQUID MEMBRANES FOR DIVALENT METAL REMOVAL/RECOVERY

    EPA Science Inventory

    The synthesis and separation properties of a mesoporous silica supported liquid membrane (SLM) were studied. The membranes consisted of a silica layer, from dip-coated colloidal silica, on a a-alumina support, modified with DCDMS (dichlorodimethyl silane) to add surface methyl g...

  8. Modeling of the mass transfer rates of metal ions across supported liquid membranes. 1: Theory

    SciTech Connect

    Elhassadi, A.A.; Do, D.D.

    1999-01-01

    This paper deals with the modeling of the transport and separation of metal ions across supported liquid membranes. The mass transfer resistance at the liquid-membrane interfaces and the interfacial chemical reactions at both the extracting side and the stripping side are taken into account in the model equations. Simple analysis of the time scale of the system shows the influence of various important parameters and their interactions on the overall transport rate. Parametric studies are also dealt with in this paper.

  9. Removal and recovery of heavy metals from wastewaters by supported liquid membranes.

    PubMed

    Yang, X J; Fane, A G; MacNaughton, S

    2001-01-01

    The removal and recovery of Cu, Cr and Zn from plating rinse wastewater using supported liquid membranes (SLM) are investigated. SLMs with specific organic extractants as the liquid membrane carriers in series are able to remove and concentrate heavy metals with very high purity, which is very promising for recycling of heavy metals in the electroplating industry. A technical comparison between the membrane process and the conventional chemical precipitation process was made. PMID:11380200

  10. A Monolithic Hybrid Cellulose-2.5-Acetate/Polymer Bioreactor for Biocatalysis under Continuous Liquid-Liquid Conditions Using a Supported Ionic Liquid Phase.

    PubMed

    Sandig, Bernhard; Michalek, Lukas; Vlahovic, Sandra; Antonovici, Mihaela; Hauer, Bernhard; Buchmeiser, Michael R

    2015-10-26

    Mesoporous monolithic hybrid cellulose-2.5-acetate (CA)/polymer supports were prepared under solvent-induced phase separation conditions using cellulose-2.5-acetate microbeads 8-14 μm in diameter, 1,1,1-tris(hydroxymethyl)propane and 4,4'-methylenebis(phenylisocyanate) as monomers as well as THF and n-heptane as porogenic solvents. 4-(Dimethylamino)pyridine and dibutyltin dilaurate (DBTDL), respectively, were used as catalysts. Monolithic hybrid supports were used in transesterification reactions of vinyl butyrate with 1-butanol under continuous, supported ionic liquid-liquid conditions with Candida antarctica lipase B (CALB) and octylmethylimidazolium tetrafluoroborate ([OMIM(+) ][BF4 (-) ]) immobilized within the CA beads inside the polymeric monolithic framework and methyl tert-butyl ether (MTBE) as the continuous phase. The new hybrid bioreactors were successfully used in dimensions up to 2×30 cm (V=94 mL). Under continuous biphasic liquid-liquid conditions a constant conversion up to 96 % was achieved over a period of 18 days, resulting in a productivity of 58 μmol mg(-1) (CALB) min(-1) . This translates into an unprecedented turnover number (TON) of 3.9×10(7) within two weeks, which is much higher than the one obtained under standard biphasic conditions using [OMIM(+) ][BF4 (-) ]/MTBE (TON=2.7×10(6) ). The continuous liquid-liquid setup based on a hybrid reactor presented here is strongly believed to be applicable to many other enzyme-catalyzed reactions. PMID:26493884

  11. Extraction of aluminum from a pickling bath with supported liquid membrane extraction

    SciTech Connect

    Berends, A.M.; Witkamp, G.J.; Rosmalen, G.M. van

    1999-04-01

    Large amounts of waste are produced yearly in the galvanic and chemical surface treatment industry. Bath liquids used in the various processes lose their function due to contamination. The spent bath liquids have to be replaced and treated prior to disposal, leading to high costs and a high environmental burden. In this paper, a proposed solution to the problem is investigated: the selective removal of the contaminant with supported liquid membrane extraction. The extraction of aluminum, a contaminant at high concentrations, from a pickling bath liquid with hydrofluoric acid and phosphoric acid as its main components has been carried out with the basic extractants Alamine 308 and Alamine 336 in a flat sheet-supported liquid membrane setup. Aluminum transport rates were obtained in the order of 10{sup {minus}6}--10{sup {minus}5} mol/(m{sup 2} {center_dot} s), which are normal values for this technique. The extraction was not completely selective as dissolved phosphorus was coextracted. In all experiments, precipitation took place on the surface of the liquid membrane and in the bulk of the strip phase. Increasing the stripping alkalinity from pH = 8 to pH = 13 reduced the amount of precipitation in the bulk of the strip phase but caused a substantial decrease in the aluminum flux. The precipitation prevents industrial application of the systems investigated.

  12. High Temperature Separation of Carbon Dioxide/Hydrogen Mixtures Using Facilitated Supported Ionic Liquid Membranes

    SciTech Connect

    Myers, C.R.; Pennline, H.W.; Luebke, D.R.; Ilconich, J.B.; Dixon, J.K.; Maginn, E.J.; Brennecke, J.F.

    2008-09-01

    Efficiently separating CO2 from H2 is one of the key steps in the environmentally responsible uses of fossil fuel for energy production. A wide variety of resources, including petroleum coke, coal, and even biomass, can be gasified to produce syngas (a mixture of COand H2). This gas stream can be further reacted with water to produce CO2 and more H2. Once separated, the CO2 can be stored in a variety of geological formations or sequestered by other means. The H2 can be combusted to operate a turbine, producing electricity, or used to power hydrogen fuel cells. In both cases, onlywater is produced as waste. An amine functionalized ionic liquid encapsulated in a supported ionic liquid membrane (SILM) can separate CO2 from H2 with a higher permeability and selectivity than any known membrane system. This separation is accomplished at elevated temperatures using facilitated transport supported ionic liquid membranes.

  13. The Effect of Microporous Polymeric Support Modification on Surface and Gas Transport Properties of Supported Ionic Liquid Membranes

    PubMed Central

    Akhmetshina, Alsu A.; Davletbaeva, Ilsiya M.; Grebenschikova, Ekaterina S.; Sazanova, Tatyana S.; Petukhov, Anton N.; Atlaskin, Artem A.; Razov, Evgeny N.; Zaripov, Ilnaz I.; Martins, Carla F.; Neves, Luísa A.; Vorotyntsev, Ilya V.

    2015-01-01

    Microporous polymers based on anionic macroinitiator and toluene 2,4-diisocyanate were used as a support for 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim][PF6]) and 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([emim][Tf2N]) immobilization. The polymeric support was modified by using silica particles associated in oligomeric media, and the influence of the modifier used on the polymeric structure was studied. The supported ionic liquid membranes (SILMs) were tested for He, N2, NH3, H2S, and CO2 gas separation and ideal selectivities were calculated. The high values of ideal selectivity for ammonia-based systems with permanent gases were observed on polymer matrixes immobilized with [bmim][PF6] and [emim][Tf2N]. The modification of SILMs by nanosize silica particles leads to an increase of NH3 separation relatively to CO2 or H2S. PMID:26729177

  14. Liquid phase methanol LaPorte process development unit: Modification, operation, and support studies

    SciTech Connect

    Not Available

    1991-02-02

    This report consists of Detailed Data Acquisition Sheets for Runs E-6 and E-7 for Task 2.2 of the Modification, Operation, and Support Studies of the Liquid Phase Methanol Laporte Process Development Unit. (Task 2.2: Alternate Catalyst Run E-6 and Catalyst Activity Maintenance Run E-7).

  15. Production of fungal antibiotics using polymeric solid supports in solid-state and liquid fermentation.

    PubMed

    Bigelis, Ramunas; He, Haiyin; Yang, Hui Y; Chang, Li-Ping; Greenstein, Michael

    2006-10-01

    The use of inert absorbent polymeric supports for cellular attachment in solid-state fungal fermentation influenced growth, morphology, and production of bioactive secondary metabolites. Two filamentous fungi exemplified the utility of this approach to facilitate the discovery of new antimicrobial compounds. Cylindrocarpon sp. LL-Cyan426 produced pyrrocidines A and B and Acremonium sp. LL-Cyan416 produced acremonidins A-E when grown on agar bearing moist polyester-cellulose paper and generated distinctly different metabolite profiles than the conventional shaken or stationary liquid fermentations. Differences were also apparent when tenfold concentrated methanol extracts from these fermentations were tested against antibiotic-susceptible and antibiotic-resistant Gram-positive bacteria, and zones of inhibition were compared. Shaken broth cultures of Acremonium sp. or Cylindrocarpon sp. showed complex HPLC patterns, lower levels of target compounds, and high levels of unwanted compounds and medium components, while agar/solid support cultures showed significantly increased yields of pyrrocidines A and B and acremonidins A-E, respectively. This method, mixed-phase fermentation (fermentation with an inert solid support bearing liquid medium), exploited the increase in surface area available for fungal growth on the supports and the tendency of some microorganisms to adhere to solid surfaces, possibly mimicking their natural growth habits. The production of dimeric anthraquinones by Penicillium sp. LL-WF159 was investigated in liquid fermentation using various inert polymeric immobilization supports composed of polypropylene, polypropylene cellulose, polyester-cellulose, or polyurethane. This culture produced rugulosin, skyrin, flavomannin, and a new bisanthracene, WF159-A, after fermentation in the presence and absence of polymeric supports for mycelial attachment. The physical nature of the different support systems influenced culture morphology and relative

  16. Supported ionic liquid membranes for removal of dioxins from high-temperature vapor streams.

    PubMed

    Kulkarni, Prashant S; Neves, Luisa A; Coelhoso, Isabel M; Afonso, Carlos A M; Crespo, João G

    2012-01-01

    Dioxins and dioxin-like chemicals are predominantly produced by thermal processes such as incineration and combustion at concentrations in the range of 10-100 ng of I-TEQ/kg (I-TEQ = international toxic equivalents). In this work, a new approach for the removal of dioxins from high-temperature vapor streams using facilitated supported ionic liquid membranes (SILMs) is proposed. The use of ceramic membranes containing specific ionic liquids, with extremely low volatility, for dioxin removal from incineration sources is proposed owing to their stability at very high temperatures. Supported liquid membranes were prepared by successfully immobilizing the ionic liquids tri-C(8)-C(10)-alkylmethylammonium dicyanamide ([Aliquat][DCA]) and 1-n-octyl-3-methylimidazolium dicyanamide ([Omim][DCA]) inside the porous structure of ceramic membranes. The porous inorganic membranes tested were made of titanium oxide (TiO(2)), with a nominal pore size of 30 nm, and aluminum oxide (Al(2)O(3)), with a nominal pore size of 100 nm. The ionic liquids were characterized, and the membrane performance was assessed for the removal of dioxins. Different materials (membrane pore size, type of ionic liquid, and dioxin) and different operating conditions (temperature and flow rate) were tested to evaluate the efficiency of SILMs for dioxin removal. All membranes prepared were stable at temperatures up to 200 °C. Experiments with model incineration gas were also carried out, and the results obtained validate the potential of using ceramic membranes with immobilized ionic liquids for the removal of dioxins from high-temperature vapor sources. PMID:22087544

  17. Supported absorption of CO2 by tetrabutylphosphonium amino acid ionic liquids.

    PubMed

    Zhang, Jianmin; Zhang, Suojiang; Dong, Kun; Zhang, Yanqiang; Shen, Youqing; Lv, Xingmei

    2006-05-15

    A new type of "task specific ionic liquid", tetrabutylphosphonium amino acid [P(C4)4][AA], was synthesized by the reaction of tetrabutylphosphonium hydroxide [P(C4)4][OH] with amino acids, including glycine, L-alanine, L-beta-alanine, L-serine, and L-lysine. The liquids produced were characterized by NMR, IR spectroscopies, and elemental analysis, and their thermal decomposition temperature, glass transition temperature, electrical conductivity, density, and viscosity were recorded in detail. The [P(C4)4][AA] supported on porous silica gel effected fast and reversible CO2 absorption when compared with bubbling CO2 into the bulk of the ionic liquid. No changes in absorption capacity and kinetics were found after four cycles of absorption/desorption. The CO2 absorption capacity at equilibrium was 50 mol % of the ionic liquids. In the presence of water (1 wt %), the ionic liquids could absorb equimolar amounts of CO2. The CO2 absorption mechanisms of the ionic liquids with and without water were different. PMID:16528787

  18. Carbon Dioxide Selective Supported Ionic Liquid Membranes: The Effect of Contaminants

    SciTech Connect

    Luebke, D.R.; Ilconich, J.B.; Myers, C.R.; Pennline, H.W.

    2008-04-01

    The integrated gasification combined cycle (IGCC) is widely viewed as a promising technology for the large scale production of energy in a carbon constrained world. These cycles, which include gasification, contaminant removal, water-gas shift, CO2 capture and compression, and combustion of the reduced-carbon fuel gas in a turbine, often have significant efficiency advantages over conventional combustion technologies. A CO2 selective membrane capable of maintaining performance at conditions approaching those of low temperature water-gas shift (260oC) could facilitate the production of carbon-neutral energy by simultaneously driving the shift reaction to completion and concentrating CO2 for sequestration. Supported ionic liquid membranes (SILMs) have been previously evaluated for this application and determined to be physically and chemically stable to temperatures in excess of 300oC. These membranes were based on ionic liquids which interacted physically with CO2 and diminished considerably in selectivity at higher temperatures. To alleviate this problem, the original ionic liquids were replaced with ionic liquids able to form chemical complexes with CO2. These complexing ionic liquid membranes have a local maximum in selectivity which is observed at increasing temperatures for more stable complexes. Efforts are currently underway to develop ionic liquids with selectivity maxima at temperatures greater than 75oC, the best result to date, but other practical concerns must also be addressed if the membrane is to be realistically expected to function under water-gas shift conditions. A CO2 selective membrane must function not only at high temperature, but also in the presence of all the reactants and contaminants likely to be present in coal-derived fuel gas, including water, CO, and H2S. A study has been undertaken which examines the effects of each of these gases on both complexing and physically interacting supported liquid membranes. In a joint project

  19. Ultra-hydrophobic ionic liquid 1-hexyl-3-methylimidazolium tris(pentafluoroethyl)trifluorophosphate supported hollow-fiber membrane liquid-liquid-liquid microextraction of chlorophenols.

    PubMed

    Ge, Dandan; Lee, Hian Kee

    2015-01-01

    An ultra-hydrophobic ionic liquid, 1-hexyl-3-methylimidazolium tris(pentafluoroethyl)trifluorophosphate ([HMIM][FAP]) was immobilized in the pores of a polypropylene hollow fiber for liquid-liquid-liquid microextraction (HF-LLLME) of chlorophenols (CPs) (4-chloro-3-methylphenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol). The analytes were first extracted from 10 ml of water sample into the ionic liquid membrane, and then were extracted back into 5 μl of sodium hydroxide aqueous solution in the hollow fiber channel. After extraction, the acceptor solution was directly injected into a high-performance liquid chromatographic system for analysis. Extraction parameters such as extraction time, salt concentration in the sample, the pH of the sample and acceptor phase, and stirring rate during extraction were investigated. The relative standard deviations of the analytes varied from 4 to 6%. Limits of detection of <0.5 ng/ml were obtained for the three analytes. The squared regression coefficients relating to the calibration curve were ≥0.9941. The proposed method was applied to the analysis of CPs in canal water. PMID:25476289

  20. Development of a Supported Emulsion Liquid Membrane System for Propionic Acid Separation in a Microgravity Environment

    NASA Technical Reports Server (NTRS)

    Li, Jin; Hu, Shih-Yao B.; Wiencek, John M.

    2001-01-01

    Perstractive fermentation is a good way to increase the productivity of bioreactors. Using Propionibacteria as the model system, the feasibility of using supported emulsion liquid membrane (SELM) for perstractive fermentation is assessed in this study. Five industrial solvents were considered as the solvent for preparing the SELM. The more polar a solvent is, the higher the partition coefficient. However, toxicity of a solvent also increases with its polarity. CO-1055 (industrial decanol/octanol blend) has the highest partition coefficient toward propionic acid among the solvents that has no molecular toxicity toward Propionibacteria. A preliminary extraction study was conducted using tetradecane as solvent in a hydrophobic hollow fiber contactor. The result confirmed that SELM eliminates the equilibrium limitation of conventional liquid-liquid extraction, and allows the use of a non-toxic solvent with low partition coefficient.

  1. Determination of phthalate ester plasticizers in the aquatic environment using hollow fibre supported liquid membranes

    NASA Astrophysics Data System (ADS)

    Mtibe, A.; Msagati, Titus A. M.; Mishra, Ajay K.; Mamba, Bhekie B.

    Phthalates are known to be carcinogenic, teratogenic as well as endocrine disruptors. The potential risk to human and animals health generated from them has drawn great attention all over the world. Hollow fibre supported liquid membrane (HFSLM) online with high pressure liquid chromatography (HPLC) was used to determine benzyl butyl phthalate (BBP), dibutyl phthalate (DBP) and Diethylhexyl phthalate (DEHP) in wastewater. Toluene, di-n-hexyl ether and undecane were used as liquid barriers separating both donor (sample) and acceptor phase. Toluene performed much better than undecane and was used in sample preparation. The presence of toluene showed the potential for the enrichment and removal of phthalates to the concentrations ranges from 0 to 1.7 mg L-1.

  2. Ignition Capsules with Aerogel-Supported Liquid DT Fuel For The National Ignition Facility

    SciTech Connect

    Ho, D D; Salmonson, J D; Clark, D S; Lindl, J D; Haan, S W; Amendt, P; Wu, K J

    2011-10-25

    For high repetition-rate fusion power plant applications, capsules with aerogel-supported liquid DT fuel can have much reduced fill time compared to {beta}-layering a solid DT fuel layer. The melting point of liquid DT can be lowered once liquid DT is embedded in an aerogel matrix, and the DT vapor density is consequently closer to the desired density for optimal capsule design requirement. We present design for NIF-scale aerogel-filled capsules based on 1-D and 2-D simulations. An optimal configuration is obtained when the outer radius is increased until the clean fuel fraction is within 65-75% at peak velocity. A scan (in ablator and fuel thickness parameter space) is used to optimize the capsule configurations. The optimized aerogel-filled capsule has good low-mode robustness and acceptable high-mode mix.

  3. Supported Room Temperature Ionic Liquid Membranes for CO{sub 2}/CH{sub 4} Separation

    SciTech Connect

    Iarikov, D. D.; Hacarlioglu, P.; Oyama, S. T.

    2011-01-01

    Room temperature ionic liquids (RTILs) are organic salts which are liquid at or around room temperature. These compounds exhibit many outstanding physical properties such as great thermal stability and no measurable vapor pressure. In this work supported ionic liquid membranes (SILMs) were prepared by impregnating pores of α-alumina inorganic supports with various ionic liquids. In addition to membranes prepared with pure RTILs we were able to synthesize membranes with RTIL mixtures using 1-aminopyridinium iodide dissolved in 1-butyl-4-methylpyridinium tetrafluoroborate or methyltrioctylammonium bis(trifluoromethylsulfonyl)imide. This combination of an RTIL with an organic salt containing an amine group dramatically improved the membrane separation properties. The SILMs displayed CO{sub 2} permeance on the order of 5 × 10{sup −10} to 5 × 10{sup −9} mol m{sup −2} s{sup −1} Pa{sup −1} combined with CO{sub 2}/CH{sub 4} selectivity of 5–30. Although these values are comparable with the current systems for CO{sub 2} purification, CO{sub 2} permeance is still rather low for these compounds.

  4. Separation of penicillin G from phenylacetic acid in a supported liquid membrane system.

    PubMed

    Lee, C J; Yeh, H J; Yang, W Y; Kan, C R

    1994-02-20

    The separation of penicillin G (Pen G) from phenylacetic acid (PAA) by use of a supported liquid membrane (SLM) system with Amberlite LA-2 dissolved in 1-decanol, supported on a microporous polypropylene membrane, was studied. The results show that the individual permeability of each component in mixture was lower than that in a single compartment system and, it suggests a strong transport competition between Pen G and PAA. The SLM system in this study proved to be a promising process for the selective separation of Pen G from PAA. The maximum separation factor was found to be 1.8 under a liquid membrane resistance controlled mechanism. (c) 1994 John Wiley & Sons, Inc. PMID:18615694

  5. Towards liquid fuels from biosyngas: effect of zeolite structure in hierarchical-zeolite-supported cobalt catalysts.

    PubMed

    Sartipi, Sina; Alberts, Margje; Meijerink, Mark J; Keller, Tobias C; Pérez-Ramírez, Javier; Gascon, Jorge; Kapteijn, Freek

    2013-09-01

    Wax on, wax off: Bifunctional cobalt-based catalysts on zeolite supports are applied for the valorization of biosyngas through Fischer-Tropsch chemistry. By using these catalysts, waxes can be hydrocracked to shorter-chain hydrocarbons, increasing the selectivity towards the C5 -C11 (gasoline) fraction. The zeolite topology and the amount and strength of acid sites are key parameters to maximize the performance of these bifunctional catalysts, steering Fischer-Tropsch product selectivity towards liquid hydrocarbons. PMID:23765635

  6. Chiroptical Probing of Lanthanide-Directed Self-Assembly Formation Using btp Ligands Formed in One-Pot Diazo-Transfer/Deprotection Click Reaction from Chiral Amines.

    PubMed

    Byrne, Joseph P; Martínez-Calvo, Miguel; Peacock, Robert D; Gunnlaugsson, Thorfinnur

    2016-01-11

    A series of enantiomeric 2,6-bis(1,2,3-triazol-4-yl)pyridines (btp)-containing ligands was synthesized by a one-pot two-step copper-catalyzed amine/alkyne click reaction. The Eu(III) - and Tb(III) -directed self-assembly formation of these ligands was studied in CH3 CN by monitoring their various photophysical properties, including their emerging circular dichroism and circularly polarized luminescence. The global analysis of the former enabled the determination of both the stoichiometry and the stability constants of the various chiral supramolecular species in solution. PMID:26555573

  7. Supported liquid membrane stability in chiral resolution by chemically and physically modified membranes.

    PubMed

    Molinari, R; Argurio, P

    2001-01-01

    In the present work some stability studies on Supported Liquid Membranes (SLMs) to be used for chiral separations were realized. In particular, primary aim was to determine how a modification of the support surface influences the SLM stability. First, the procedure for support modification was optimised, making a screening of various compounds (sulphuric acid, nitric acid, chromic acid, sodium dodecyl sulphate (SDS), glycerol, oleic alcohol, propylene glycol (PPG), bovine serum albumin (BSA)) and testing their performance by means of contact angle measurements. Next, a second screening was realized by permeation tests in a stirred cell. Finally, to compare the stability of modified with unmodified support in a process of interest for chemical and/or biochemical industries, some permeation tests for resolution of DNB-DL-Leucine were realized in a re-circulation system. Results showed a better surface hydrophilization of chemically modified support and better stability of the sulphonated support. However, in operating conditions a little high stability of the unmodified support was obtained. PMID:11381544

  8. Computing UV/vis spectra using a combined molecular dynamics and quantum chemistry approach: bis-triazin-pyridine (BTP) ligands studied in solution.

    PubMed

    Höfener, Sebastian; Trumm, Michael; Koke, Carsten; Heuser, Johannes; Ekström, Ulf; Skerencak-Frech, Andrej; Schimmelpfennig, Bernd; Panak, Petra J

    2016-03-21

    We report a combined computational and experimental study to investigate the UV/vis spectra of 2,6-bis(5,6-dialkyl-1,2,4-triazin-3-yl)pyridine (BTP) ligands in solution. In order to study molecules in solution using theoretical methods, force-field parameters for the ligand-water interaction are adjusted to ab initio quantum chemical calculations. Based on these parameters, molecular dynamics (MD) simulations are carried out from which snapshots are extracted as input to quantum chemical excitation-energy calculations to obtain UV/vis spectra of BTP ligands in solution using time-dependent density functional theory (TDDFT) employing the Tamm-Dancoff approximation (TDA). The range-separated CAM-B3LYP functional is used to avoid large errors for charge-transfer states occurring in the electronic spectra. In order to study environment effects with theoretical methods, the frozen-density embedding scheme is applied. This computational procedure allows to obtain electronic spectra calculated at the (range-separated) DFT level of theory in solution, revealing solvatochromic shifts upon solvation of up to about 0.6 eV. Comparison to experimental data shows a significantly improved agreement compared to vacuum calculations and enables the analysis of relevant excitations for the line shape in solution. PMID:26907588

  9. Supported liquid membrane-liquid chromatography-mass spectrometry analysis of cyanobacterial toxins in fresh water systems

    NASA Astrophysics Data System (ADS)

    Mbukwa, Elbert A.; Msagati, Titus A. M.; Mamba, Bhekie B.

    Harmful algal blooms (HABs) are increasingly becoming of great concern to water resources worldwide due to indiscriminate waste disposal habits resulting in water pollution and eutrophication. When cyanobacterial cells lyse (burst) they release toxins called microcystins (MCs) that are well known for their hepatotoxicity (causing liver damage) and have been found in eutrophic lakes, rivers, wastewater ponds and other water reservoirs. Prolonged exposure to low concentrated MCs are equally of health importance as they are known to be bioaccumulative and even at such low concentration do exhibit toxic effects to aquatic animals, wildlife and human liver cells. The application of common treatment processes for drinking water sourced from HABs infested reservoirs have the potential to cause algal cell lyses releasing low to higher amounts of MCs in finished water. Trace microcystins in water/tissue can be analyzed and quantified using Liquid chromatography-electrospray ionization-mass spectrometry (LC-ESI-MS) following solid-phase extraction (SPE) sample clean-up procedures. However, extracting MCs from algal samples which are rich in chlorophyll pigments and other organic matrices the SPE method suffers a number of drawbacks, including cartridge clogging, long procedural steps and use of larger volumes of extraction solvents. We applied a supported liquid membrane (SLM) based technique as an alternative sample clean-up method for LC-ESI-MS analysis of MCs from both water and algal cells. Four (4) MC variants (MC-RR, -YR, -LR and -WR) from lyophilized cells of Microcystis aeruginosa and water collected from a wastewater pond were identified) and quantified using LC-ESI-MS following a SLM extraction and liquid partitioning step, however, MC-WR was not detected from water extracts. Within 45 min of SLM extraction all studied MCs were extracted and pre-concentrated in approximately 15 μL of an acceptor phase at an optimal pH 2.02 of the donor phase (sample). The highest

  10. Molecular recognition of carbohydrates by a resorcinarene. Selective transport of alditols through a supported liquid membrane.

    PubMed

    Tbeur, N; Rhlalou, T; Hlaïbi, M; Langevin, D; Métayer, M; Verchère, J F

    2000-11-01

    A supported liquid membrane (SLM) containing a resorcinarene carrier has been used for the selective transport of erythritol, threitol, ribitol and xylitol from concentrated (1.0-0.01 M) aqueous solutions. The membrane is made of a microporous polytetrafluoroethylene film impregnated with a 0.01 M solution of the carrier in CCl4. The permeabilities of the SLM for all alditols were calculated. On the basis of the flux dependence on the initial concentrations of carrier and alditol, the rate-determining step in the transport mechanism is shown to be the migration of the 1:1 carrier-carbohydrate complex in the immobilized organic phase. The flux of sugar is related to the initial concentration of alditol in the feed phase by a saturation law, which allowed the determination of the apparent diffusion coefficients and the stability constants of the resorcinarene complexes of alditols formed in the liquid membrane. PMID:11117324

  11. SUPPORTED LIX-84 LIQUID MEMBRANES FOR METAL ION SEPARATION: A STUDY ON METAL ION SORPTION EQUILIBRIUM AND KINETICS

    EPA Science Inventory

    Supported 2-hydroxy-5-nonyl-acetophenone oxime (LIX-84) liquid membranes have potential applications for the removal (or recovery) of copper ions from waste streams. But, the stability of such a liquid membrane remains the major hurdle for its practical applications. Inorganic su...

  12. Supported liquid membranes in radioactive waste treatment processes: Recent experience and perspective

    SciTech Connect

    Nechaev, A.F.; Projaev, V.V.; Kapranchik, V.P.

    1995-12-31

    Recent experience in practical application of Supported Liquid Membranes (SLM or SUPLIM) both in the hydrometallurgy and nuclear technology has been analyzed. The results obtained allow one to consider SUPLIM as a promising technology for radioactive waste treatment. This statement is based on the evaluation of integrated socioeconomic effects, including quantity of additional chemicals, the volume of secondary technological streams and secondary wastes, simplicity and the low costs of equipment used, potential possibility to organize in situ process, and the level of the harmful impact on personnel. 35 refs.

  13. SUPPORTED LIQUID CATALYSTS FOR REMOVAL OF HIGH TEMPERATURE FUEL CELL CONTAMINANTS

    SciTech Connect

    Alan W. Weimer; Peter Czerpak; Patrick Hilbert

    2000-01-01

    A novel catalytic synthesis gas oxidation process using molten carbonate salts supported on compatible fluidized iron oxide particles (supported-liquid-phase-catalyst (SLPC) fluidized bed process) was investigated. This process combines the advantages of large scale fluidized bed processing with molten salt bath oxidation. Molten salt catalysts can be supported within porous fluidized particles in order to improve mass transfer rates between the liquid catalysts and the reactant gases. Synthesis gas can be oxidized at reduced temperatures resulting in low NO{sub x} formation while trace sulfides and halides are captured in-situ. Hence, catalytic oxidation of synthesis gas can be carried out simultaneously with hot gas cleanup. Such SLPC fluidized bed processes are affected by inter-particle liquid capillary forces that may lead to agglomeration and de-fluidization of the bed. An understanding of the origin and strength of these forces is needed so that they can be overcome in practice. Process design is based on thermodynamic free energy minimization calculations that indicate the suitability of eutectic Na{sub 2}CO{sub 3}/K{sub 2}CO{sub 3} mixtures for capturing trace impurities in-situ (< 1 ppm SO{sub x} released) while minimizing the formation of NO{sub x}(< 10 ppm). Iron oxide has been identified as a preferred support material since it is non-reactive with sodium, is inexpensive, has high density (i.e. inertia), and can be obtained in various particle sizes and porosities. Force balance modeling has been used to design a surrogate ambient temperature system that is hydrodynamically similar to the real system, thus allowing complementary investigation of the governing fluidization hydrodynamics. The primary objective of this research was to understand the origin of and to quantify the liquid capillary interparticle forces affecting the molten carbonate SLPC fluidized bed process. Substantial theoretical and experimental exploratory results indicate process

  14. Summary of Liquid Propulsion System Needs in Support of the Constellation Program

    NASA Technical Reports Server (NTRS)

    Lorier, Terry; Sumrall, Phil; Baine, Michael

    2008-01-01

    In January 2004, the President of the United States established the Vision for Space Exploration (VSE) to complete the International Space Station, retire the Space Shuttle and develop its replacement, and expand the human presence on the Moon as a stepping stone to human exploration of Mars and worlds beyond. In response, NASA developed the Constellation Program, consisting of the components shown in Figure 1. This paper will summarize the manned spaceflight liquid propulsion system needs in support of the Constellation Program over the next 10 years. It will address all liquid engine needs to support human exploration from low Earth orbit (LEO) to the lunar surface, including an overview of engines currently under contract, those baselined but not yet under contract, and those propulsion needs that have yet to be initiated. There may be additional engine needs for early demonstrators, but those will not be addressed as part of this paper. Also, other portions of the VSE architecture, including the planned Orion abort test boosters and the Lunar Precursor Robotic Program, are not addressed here as they either use solid motors or are focused on unmanned elements of returning humans to the Moon.

  15. New support for high-performance liquid chromatography based on silica coated with alumina particles.

    PubMed

    Silveira, José Leandro R; Dib, Samia R; Faria, Anizio M

    2014-01-01

    A new material based on silica coated with alumina nanoparticles was proposed for use as a chromatographic support for reversed-phase high-performance liquid chromatography. Alumina nanoparticles were synthesized by a sol-gel process in reversed micelles composed of sodium bis(2-ethylhexyl)sulfosuccinate, and the support material was formed by the self-assembly of alumina layers on silica spheres. Spectroscopic and (29)Si nuclear magnetic resonance results showed evidence of chemical bonds between the alumina nanoparticles and the silica spheres, while morphological characterizations showed that the aluminized silica maintained the morphological properties of silica desired for chromatographic purposes after alumina incorporation. Stability studies indicated that bare silica showed high dissolution (~83%), while the aluminized silica remained practically unchanged (99%) after passing one liter of the alkaline mobile phase, indicating high stability under alkaline conditions. The C18 bonded aluminized silica phase showed great potential for use in high-performance liquid chromatography to separate basic molecules in the reversed-phase mode. PMID:24521917

  16. Liquid phase catalytic hydrodebromination of tetrabromobisphenol A on supported Pd catalysts

    NASA Astrophysics Data System (ADS)

    Wu, Ke; Zheng, Mengjia; Han, Yuxiang; Xu, Zhaoyi; Zheng, Shourong

    2016-07-01

    Tetrabromobisphenol A (TBBPA) is a widely used brominated flame retardant and reductive debromination is an effective method for the abatement of TBBPA pollution. In this study, Pd catalysts supported on TiO2, CeO2, Al2O3 and SiO2 were prepared by the impregnation (the resulting catalyst denoted as im-Pd/support), deposition-precipitation (the resulting catalyst denoted as dp-Pd/support), and photo-deposition (the resulting catalyst denoted as pd-Pd/support) methods. The catalysts were characterized by N2 adsorption-desorption isotherm, X-ray diffraction, transmission electron microscopy, measurement of zeta potential, CO chemisorption, and X-ray photoelectron spectroscopy. The results showed that at an identical Pd loading amount (2.0 wt.%) Pd particle size in dp-Pd/TiO2 was much smaller than those in im-Pd/TiO2 and pd-Pd/TiO2. Pd particle size of the dp-Pd/TiO2 catalyst increased with Pd loading amount. Additionally, Pd particles in the dp-Pd/TiO2 catalysts were positively charged due to the strong metal-support interaction, whereas the cationization effect was gradually attenuated with the increase of Pd loading amount. For the liquid phase catalytic hydrodebromination (HDB) of TBBPA, tri-bromobisphenol A (tri-BBPA), di-bromobisphenol A (di-BBPA), and mono-bromobisphenol A (mono-BBPA) were identified as the intermediate products, indicative of a stepwise debromination process. The catalytic HDB of TBBPA followed the Langmuir-Hinshelwood model, reflecting an adsorption enhanced catalysis mechanism. At an identical Pd loading amount, the Pd catalyst supported on TiO2 exhibited a much higher catalytic activity than those on other supports. Furthermore, dp-Pd/TiO2 was found to be more active than im-Pd/TiO2 and pd-Pd/TiO2.

  17. Advanced Supported Liquid Membranes for Carbon Dioxide Control in Cabin Applications

    NASA Technical Reports Server (NTRS)

    Wickham, David T.; Gleason, Kevin J.; Engel, Jeffrey R.; Chullen, Cinda

    2016-01-01

    The development of new, robust, life support systems is critical to NASA's continued progress in space exploration. One vital function is maintaining the carbon dioxide (CO2) concentration in the cabin at levels that do not impair the health or performance of the crew. The CO2 removal assembly (CDRA) is the current CO2 control technology on-board the International Space Station (ISS). Although the CDRA has met the needs of the ISS to date, the repeated cycling of the molecular sieve sorbent causes it to break down into small particles that clog filters or generate dust in the cabin. This reduces reliability and increases maintenance requirements. Another approach that has potential advantages over the current system is a membrane that separates CO2 from air. In this approach, cabin air contacts one side of the membrane while other side of the membrane is maintained at low pressure to create a driving force for CO2 transport across the membrane. In this application, the primary power requirement is for the pump that creates the low pressure and then pumps the CO2 to the oxygen recovery system. For such a membrane to be practical, it must have high CO2 permeation rate and excellent selectivity for CO2 over air. Unfortunately, conventional gas separation membranes do not have adequate CO2 permeability and selectivity to meet the needs of this application. However, the required performance could be obtained with a supported liquid membrane (SLM), which consists of a microporous material filled with a liquid that selectively reacts with CO2 over air. In a recently completed Phase II SBIR project, Reaction Systems, Inc. fabricated an SLM that is very close to meeting permeability and selectivity objectives for use in the advanced space suit portable life support system. This paper describes work carried out to evaluate its potential for use in spacecraft cabin application.

  18. The application of supported liquid extraction in the analysis of benzodiazepines using surface enhanced Raman spectroscopy.

    PubMed

    Doctor, Erika L; McCord, Bruce

    2015-11-01

    Benzodiazepines are among the most frequently prescribed medicines for anxiety disorders and are present in many toxicological screens. These drugs are often administered in the commission of drug facilitated sexual assaults due their effects on the central nervous system. Due to the potency of the drugs, only small amounts are usually given to victims; therefore, the target detection limit for these compounds in biological samples has been set at 50 ng/mL. Currently the standard screening method for detection of this class of drug is the immunoassay; however, screening methods that are more sensitive and selective than immunoassays are needed to encompass the wide range of structural variants of this class of compounds. Surface enhanced Raman spectroscopy (SERS) can be highly sensitive and has been shown to permit analysis of various benzodiazepines with limits of detection as low as 6 ng/mL. This technique permits analytical results in less than 2 min when used on pure drug samples. For biological samples, a key issue for analysis by SERS is removal of exogenous salts and matrix components. In this paper we examine supported liquid extraction as a useful preparation technique for SERS detection. Supported liquid extraction has many of the benefits of liquid-liquid extraction along with the ability to be automated. This technique provides a fast and clean extraction for benzodiazepines from urine at a pH of 5.0, and does not produce large quantities of solvent waste. To validate this procedure we have determined figures of merit and examined simulated urine samples prepared with commonly appearing interferences. It was shown that at a pH 5.0 many drugs that are prevalent in urine samples can be removed, permitting a selective detection of the benzodiazepine of interest. This technique has been shown to provide rapid (less than 20 min), sensitive, and specific detection of benzodiazepines with limits of detection between 32 and 600 ng/mL and dynamic range of 32

  19. Supported Phospholipid Bilayer Defects Created by a Cation or Anion of a Room-Temperature Ionic Liquid

    Technology Transfer Automated Retrieval System (TEKTRAN)

    In this work, the independent effects on a supported phospholipid bilayer (SPB) caused by a cation and anion of a room-temperature ionic liquid (RT-IL) were studied via atomic force microscopy (AFM). The supported phospholipid bilayer was composed only of 1,2-dielaidoylphosphatidylcholine (DEPC) an...

  20. Supported liquid membrane-protected molecularly imprinted fibre for solid-phase microextraction of thiabendazole.

    PubMed

    Barahona, Francisco; Turiel, Esther; Martín-Esteban, Antonio

    2011-05-23

    In this work, molecularly imprinted polymer fibres (MIP-fibre) have been prepared and evaluated for solid-phase microextraction (SPME), using thiabendazole (TBZ) as template. Inherent limitations of molecular imprinted polymers, such as target recognition in aqueous media, have been solved with the use of organic supported liquid membrane (SLM) protecting the MI-SPME process. MIP-fibres were located inside a polypropylene hollow capillary and protected by an organic solvent immobilized as a thin SLM in the pores of the capillary wall. The extraction procedure involved two simultaneous processes: liquid phase microextraction using polypropylene hollow fibres (HF-LPME) of the analytes from the sample to an organic acceptor solution through a SLM; and SPME of the analytes from the organic acceptor solution to a MIP-fibre inside the polypropylene capillary. The developed methodology was optimized and applied to the extraction of TBZ form spiked orange juices. Calibration curves showed good linearity in the concentration range under study (0.01-5.00 mg L(-1)) and a regression coefficient better than 0.995 was obtained. The detection limit was 4 μg L(-1), low enough to permit the satisfactory analysis of TBZ in real samples, according to European regulation. Relative standard deviations ranged below 10%, indicating good repeatability. By this manner, the advantages of inherent selectivity of MIP SPME fibres and the enrichment and sample cleanup capability of the HF-LPME have been successfully combined into a single device. PMID:21565306

  1. Some methods of human liquid and solid wastes utilization in bioregenerative life support systems

    NASA Astrophysics Data System (ADS)

    Tikhomirova, N. A.; Ushakova, S. Á.; Tikhomirov, A. Á.; Zolotukhin, I. G.; Gribovskaya, I. V.; Gros, J. B.

    The possibility of stepwise utilization of human liquid and solid wastes with the purpose of an increase of a closure degree of bioregenerative life support systems BLSS and sodium chloride inclusion in the organic matter turnover was investigated On the first stage urine and faeces were subjected to oxidation by Yu A Kudenko physicochemical method On the next stage the products of human liquid and solid wastes oxidation were used for roots nutrition of wheat grown by substrate culture method Soil-like substrate the technology of which was described earlier was used as a substrate After the wheat cultivation the irrigational solution and the solution obtained in the result of substrate washing containing mineral elements not absorbed by the plants were used for cultivation of salt-tolerant Salicornia europaea plants The above-ground biomass of these vegetables can be used as a food and roots washed from dissoluble mineral elements can be added to the soil-like substrate Four consecutive wheat and Salicornia europaea vegetations were cultivated In the result of this complex technology of wheat and Salicornia europaea cultivation the soil-like substrate salinization by NaCl introduced into the irrigational solution together with the products of urine oxidation has considerably decreased

  2. Life Support Catalyst Regeneration Using Ionic Liquids and In Situ Resources

    NASA Technical Reports Server (NTRS)

    Abney, Morgan B.; Karr, Laurel J.; Paley, Mark S.; Donovan, David N.; Kramer, Teersa J.

    2016-01-01

    Oxygen recovery from metabolic carbon dioxide is an enabling capability for long-duration manned space flight. Complete recovery of oxygen (100%) involves the production of solid carbon. Catalytic approaches for this purpose, such as Bosch technology, have been limited in trade analyses due in part to the mass penalty for high catalyst resupply caused by carbon fouling of the iron or nickel catalyst. In an effort to mitigate this challenge, several technology approaches have been proposed. These approaches have included methods to prolong the life of the catalysts by increasing the total carbon mass loading per mass catalyst, methods for simplified catalyst introduction and removal to limit the resupply container mass, methods of using in situ resources, and methods to regenerate catalyst material. Research and development into these methods is ongoing, but only use of in situ resources and/or complete regeneration of catalyst material has the potential to entirely eliminate the need for resupply. The use of ionic liquids provides an opportunity to combine these methods in a technology approach designed to eliminate the need for resupply of oxygen recovery catalyst. Here we describe the results of an initial feasibility study using ionic liquids and in situ resources for life support catalyst regeneration, we discuss the key challenges with the approach, and we propose future efforts to advance the technology.

  3. Computational Fluid Dynamics in Support of the SNS Liquid Mercury Thermal-Hydraulic Analysis

    SciTech Connect

    Siman-Tov, M.; Wendel, M.W.; Yoder, G.L.

    1999-11-14

    Experimental and computational thermal-hydraulic research is underway to support the liquid mercury target design for the Spallation Neutron Source (SNS) facility. The SNS target will be subjected to internal nuclear heat generation that results from pulsed proton beam collisions with the mercury nuclei. Recirculation and stagnation zones within the target are of particular concern because of the likelihood that they will result in local hot spots and diminished heat removal from the target structure. Computational fluid dynamics (CFD) models are being used as a part of this research. Recent improvements to the 3D target model include the addition of the flow adapter which joins the inlet/outlet coolant pipes to the target body and an updated heat load distribution at the new baseline proton beam power level of 2 MW. Two thermal-hydraulic experiments are planned to validate the CFD model.

  4. Size stabilization of surface-supported liquid aerosols using tapered optical fiber coupling.

    PubMed

    Karadag, Yasin; Jonáš, Alexandr; Kucukkara, Ibrahim; Kiraz, Alper

    2013-03-01

    We demonstrate long-term size stabilization of surface-supported liquid aerosols of salt-water. Single tapered optical fibers were used to couple the light from independent heating and probe lasers into individual microdroplets that were kept on a superhydrophobic surface in a high-humidity chamber. Size stabilization of microdroplets resulted from competition between resonant absorption of the infrared heating laser by a microdroplet whispering gallery mode and water condensation in the sample chamber. Microdroplet size was continuously monitored using the tunable red probe laser. Thanks to the narrow linewidth of the heating laser, stabilization of the 110 μm radius of a microdroplet with a precision down to 0.54 nm was achieved for a period of 410 s. PMID:23455301

  5. Transport of europium through supported liquid membrane containing dihexyl-N,N-diethyl-carbamoyl-methyl-phosphonate

    SciTech Connect

    Nakamura, Shigeto; Akiba, Kenichi )

    1989-12-01

    The transport of europium has been studied through a supported liquid membrane (SLM) impregnated with dihexyl-N,N-diethyl-carbamoyl-methyl-phosphonate (CMP). Europium was effectively extracted from the perchlorate solution into SLM, but was insufficiently stripped to a dilute acid solution. The addition of 1-decanol improved the stripping process, and quantitative transport of europium was achieved. By the combination of two SLM systems consisting of diisodecylphosphoric acid and CMP, europium was transported from the feed solution (0.1 M HNO{sub 3}) through the intermediate solution (1 M HClO{sub 4} + 4 M NaClO{sub 4}) to the product solution (0.1 M HNO{sub 3}) and effectively concentrated by a factor of about 20.

  6. Transport of silver(I) ion through a supported liquid membrane using bathocuproine as a carrier

    SciTech Connect

    Saito, Takashi

    1998-04-01

    The active transport of silver ions through a supported liquid membrane (SLM) containing bathocuproine (4,7-diphenyl-2,9-dimethyl-1,10-phenanthroline) as a carrier was investigated under various experimental conditions. The magnitude of the permeation velocity of metallic ions through the SLM was in the order Ag{sup +} > Cd{sup 2+} {much_gt} Zn{sup 2+} > Cu{sup 2+} when nitrite ion was used as the pairing ion species that is cotransported with metallic ion. The permeation velocity of silver(I) ions through an SLM was dependent on the concentrations of the silver ion, bathocuproine, and nitrite ion. An equation for the transport of silver ions, consisting of three important factors, i.e., the concentrations of metallic ion, carrier, and pairing ion species, was derived.

  7. Transport of cadmium(II) ion through a supported liquid membrane containing a bathocuproine

    SciTech Connect

    Saito, Takashi )

    1991-12-01

    The active transport of cadmium ions across a supported liquid membrane (SLM) containing a ligand based on a driving force supplied by the concentration gradient of the chloride ion is described. The SLM used is a microporous polypropylene membrane impregnated with a bathocuproine (4,7-diphenyl-2,9-dimethyl-1,10-phenanthroline) solution in dibenzyl ether as a carrier. The characteristics of the cadmium ion transport system are examined under various experimental conditions. The active transport of cadmium ions through an SLM is dependent on the concentrations of the cadmium ion, ligand, and chloride ion. An equation for the permeation velocity of cadmium ions, consisting of three important factors for this transport system, is proposed.

  8. Continuous flow hydroformylation using supported ionic liquid phase catalysts with carbon dioxide as a carrier.

    PubMed

    Hintermair, Ulrich; Gong, Zenxing; Serbanovic, Ana; Muldoon, Mark J; Santini, Catherine C; Cole-Hamilton, David J

    2010-09-28

    A supported ionic liquid phase (SILP) catalyst prepared from [PrMIM][Ph(2)P(3-C(6)H(4)SO(3))] (PrMIM = 1-propyl-3-methylimidazolium), [Rh(CO)(2)(acac)] (acacH = 2,4-pentanedione) [OctMIM]NTf(2) (OctMIM = 1-n-octyl-3-methylimidazolium, Tf = CF(3)SO(2)) and microporous silica has been used for the continuous flow hydroformylation of 1-octene in the presence of compressed CO(2). Statistical experimental design was used to show that the reaction rate is neither much affected by the film thickness (IL loading) nor by the syngas:substrate ratio. However, a factor-dependent interaction between the syngas:substrate ratio and film thickness on the reaction rate was revealed. Increasing the substrate flow led to increased reaction rates but lower overall yields. One of the most important parameters proved to be the phase behaviour of the mobile phase, which was studied by varying the reaction pressure. At low CO(2) pressures or when N(2) was used instead of CO(2) rates were low because of poor gas diffusion to the catalytic sites in the SILP. Furthermore, leaching of IL and Rh was high because the substrate is liquid and the IL had been designed to dissolve in it. As the CO(2) pressure was increased, the reaction rate increased and the IL and Rh leaching were reduced, because an expanded liquid phase developed. Due to its lower viscosity the expanded liquid allows better transport of gases to the catalyst and is a poorer solvent for the IL and the catalyst because of its reduced polarity. Above 100 bar (close to the transition to a single phase at 106 bar), the rate of reaction dropped again with increasing pressure because the flowing phase becomes a better and better solvent for the alkene, reducing its partitioning into the IL film. Under optimised conditions, the catalyst was shown to be stable over at least 40 h of continuous catalysis with a steady state turnover frequency (TOF, mol product (mol Rh)(-1)) of 500 h(-1) at low Rh leaching (0.2 ppm). The selectivity of the

  9. Silica-particle-supported zwitterionic polymer monolith for microcolumn liquid chromatography.

    PubMed

    An, Ran; Weng, Qianfeng; Li, Jinxiang

    2014-10-01

    A silica-particle-supported zwitterionic polymeric monolithic column, shortened as supported column (S-column), was prepared by the in situ polymerization of methacrylic acid, ethylene dimethacrylate, and 2-(dimethylamino)ethyl methacrylate in the presence of a ternary porogenic solvent containing water, methanol, and cyclohexanol in a 250 μm id fused-silica capillary prepacked with 5 μm bare silica particles. In the S-column, a thin layer of the polymers was formed around the silica particles in the form of nanoglobules, leaving the interstitial spaces between the particles free for liquid flow. The effects of the preparation conditions on the morphology of the monolith were investigated by scanning electron microscopy and backpressure measurements. The selected volumetric ratio of porogens, monomer concentration, polymerization time, and temperature are 1:1:8 (water/methanol/cyclohexanol), 25% v/v, 5 h, and 60°C, respectively. The S-column was evaluated by comparison with its conventional organic counterpart in terms of morphology, mechanical stability, permeability, swelling-shrinking behavior, capacity, and efficiency. The results demonstrate that the S-column is superior to its counterpart in all the terms with the exception of permeability. The above merits and zwitterionic property of the S-column were further confirmed by separate separations of four inorganic anions and three organic cations. PMID:25044794

  10. Application of supported liquid membranes for removal of uranium from groundwater

    SciTech Connect

    Chiarizia, R.; Horwitz, E.P.; Rickert, P.G.; Hodgson, K.M.; Westinghouse Hanford Co., Richland, WA )

    1989-01-01

    The separation of uranium from Hanford site groundwater as studied by hollow-fiber supported liquid membranes, SLM. The carrier bis(2,4,4-trimethylpentyl)phosphinic acid, H(DTMPep), contained in the commercial extractant Cyanex{trademark} 272 was used as a membrane carrier, because of its selectivity for U over calcium and magnesium. The water soluble complexing agent, 1-hydroxyethane-1,1-diphosphonic acid, HEDPA, was used as stripping agent. Polypropylene hollow-fibers and n-dodecane were used as polymeric support and diluent, respectively. Laboratory scale hollow-fiber modules were employed in a recycling mode, using as feed synthetic groundwater at pH 2, to confirm the capability of the proposed SLM system to separate and concentrate U(VI) in the strip solution. Information was obtained on the U(VI) concentration factor and on the long-term performance of the SLMs. Encouraging results were obtained both with a conventional module and with a module containing a carrier solution reservoir. Industrial scale modules were used at Hanford to test the SLM separation of U(VI) from real contaminated groundwater. The uranium concentration was reduced from approximately 3500 ppB to about 1 ppB in a few hours. 9 refs., 8 figs., 4 tabs.

  11. Some methods for human liquid and solid waste utilization in bioregenerative life-support systems.

    PubMed

    Ushakova, S A; Zolotukhin, I G; Tikhomirov, A A; Tikhomirova, N A; Kudenko, Yu A; Gribovskaya, I V; Balnokin, Yu; Gros, J B

    2008-12-01

    Bioregenerative life-support systems (BLSS) are studied for developing the technology for a future biological life-support system for long-term manned space missions. Ways to utilize human liquid and solid wastes to increase the closure degree of BLSS were investigated. First, urine and faeces underwent oxidation by Kudenko's physicochemical method. The products were then used for root nutrition of wheat grown by the soil-like substrate culture method. Two means of eliminating sodium chloride, introduced into the irrigation solution together with the products of urine oxidation, were investigated. The first was based on routine electrodialysis of irrigation water at the end of wheat vegetation. Dialysis eliminated about 50% of Na from the solution. This desalinization was performed for nine vegetations. The second method was new: after wheat cultivation, the irrigation solution and the solution obtained by washing the substrate containing mineral elements not absorbed by the plants were used to grow salt-tolerant Salicornia europaea L. plants (saltwort). The above-ground biomass of this plant can be used as a food, and roots can be added to the soil-like substrate. Four consecutive wheat and Salicornia vegetations were cultivated. As a result of this wheat and Salicornia cultivation process, the soil-like substrate salinization by NaCl were considerably decreased. PMID:18581263

  12. Glycine enhanced separation of Co(II) and Ni(II) with bis(2,4,4-trimethylpentyl)phosphinic acid (Cyanex 272) by liquid-liquid extraction and supported liquid membranes

    SciTech Connect

    Reichley-Yinger, L.; Danesi, P.R.

    1985-01-01

    The extraction behavior of Co and Ni ions from aqueous nitrate solution containing glycine, and their separation by liquid-liquid extraction and supported liquid membranes (SLMs) has been studied. The separation factor between the two metals is greatly enhanced by the presence of glycine. The enhancement is due to the preferential complexation of the Ni ions by glycine. The conditional equilibrium constants of the extraction reactions and the SLM permeability coefficients have been measured. The results indicate that metal glycinate complexes are not extracted and that in presence of glycine very clean Co-Ni separation can be obtained in a single SLM pass.

  13. Direct determination of chlorophenols present in liquid samples by using a supported liquid membrane coupled in-line with capillary electrophoresis equipment.

    PubMed

    Almeda, S; Nozal, L; Arce, L; Valcárcel, M

    2007-03-21

    Actually there is a great trend on the development of effective analytical methods for monitoring trace levels of various phenols which can indicate, among others compounds, the water quality. A simple, inexpensive supported liquid membrane (SLM) device was used in combination with commercially available capillary electrophoresis (CE) equipment for the direct determination of chlorophenols in surface water samples. The manifold was used simultaneously to extract and preconcentrate the analytes from liquid samples. In the extraction set-up, the donor phase (4 mL) was placed in the CE vial, where a micro-membrane extraction unit (MMEU) accommodating the acceptor phase (100 microL) in its lumen was immersed. The supported liquid membrane was constructed by impregnating a porous Fluoropore Teflon (PTFE) membrane with a water-immiscible organic solvent (dihexyl ether). The extraction process was optimized with regard to the pH of the donor and acceptor phases, membrane liquid, extraction time and voltage applied to the inlet or outlet vial during extraction. The chlorinated phenols pentachlorophenol (PCP), 2,3,6 trichlorophenol (TCP) and 2,6 dichlorophenol (DCP) were thus efficiently separated by CE, using tris(hydroxymethyl)aminomethane (Tris) and an NaH(2)PO(4) solution containing 1% (v/v) methanol at pH 10.5 as running buffer. PMID:17386759

  14. An electrochemical gas sensor based on paper supported room temperature ionic liquids.

    PubMed

    Dossi, Nicolò; Toniolo, Rosanna; Pizzariello, Andrea; Carrilho, Emanuel; Piccin, Evandro; Battiston, Simone; Bontempelli, Gino

    2012-01-01

    A sensitive and fast-responding membrane-free amperometric gas sensor is described, consisting of a small filter paper foil soaked with a room temperature ionic liquid (RTIL), upon which three electrodes are screen printed with carbon ink, using a suitable mask. It takes advantage of the high electrical conductivity and negligible vapour pressure of RTILs as well as their easy immobilization into a porous and inexpensive supporting material such as paper. Moreover, thanks to a careful control of the preparation procedure, a very close contact between the RTIL and electrode material can be achieved so as to allow gaseous analytes to undergo charge transfer just as soon as they reach the three-phase sites where the electrode material, paper supported RTIL and gas phase meet. Thus, the adverse effect on recorded currents of slow steps such as analyte diffusion and dissolution in a solvent is avoided. To evaluate the performance of this device, it was used as a wall-jet amperometric detector for flow injection analysis of 1-butanethiol vapours, adopted as the model gaseous analyte, present in headspace samples in equilibrium with aqueous solutions at controlled concentrations. With this purpose, the RTIL soaked paper electrochemical detector (RTIL-PED) was assembled by using 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide as the wicking RTIL and printing the working electrode with carbon ink doped with cobalt(II) phthalocyanine, to profit from its ability to electrocatalyze thiol oxidation. The results obtained were quite satisfactory (detection limit: 0.5 μM; dynamic range: 2-200 μM, both referring to solution concentrations; correlation coefficient: 0.998; repeatability: ±7% RSD; long-term stability: 9%), thus suggesting the possible use of this device for manifold applications. PMID:22076475

  15. An Efficient, Versatile, and Safe Access to Supported Metallic Nanoparticles on Porous Silicon with Ionic Liquids

    PubMed Central

    Darwich, Walid; Haumesser, Paul-Henri; Santini, Catherine C.; Gaillard, Frédéric

    2016-01-01

    The metallization of porous silicon (PSi) is generally realized through physical vapor deposition (PVD) or electrochemical processes using aqueous solutions. The former uses a strong vacuum and does not allow for a conformal deposition into the pores. In the latter, the water used as solvent causes oxidation of the silicon during the reduction of the salt precursors. Moreover, as PSi is hydrophobic, the metal penetration into the pores is restricted to the near-surface region. Using a solution of organometallic (OM) precursors in ionic liquid (IL), we have developed an easy and efficient way to fully metallize the pores throughout the several-µm-thick porous Si. This process affords supported metallic nanoparticles characterized by a narrow size distribution. This process is demonstrated for different metals (Pt, Pd, Cu, and Ru) and can probably be extended to other metals. Moreover, as no reducing agent is necessary (the decomposition in an argon atmosphere at 50 °C is fostered by surface silicon hydride groups borne by PSi), the safety and the cost of the process are improved. PMID:27271608

  16. Carbon-supported ionic liquids as innovative adsorbents for CO₂ separation from synthetic flue-gas.

    PubMed

    Erto, Alessandro; Silvestre-Albero, Ana; Silvestre-Albero, Joaquín; Rodríguez-Reinoso, Francisco; Balsamo, Marco; Lancia, Amedeo; Montagnaro, Fabio

    2015-06-15

    Fixed-bed thermodynamic CO2 adsorption tests were performed in model flue-gas onto Filtrasorb 400 and Nuchar RGC30 activated carbons (AC) functionalized with [Hmim][BF4] and [Emim][Gly] ionic liquids (IL). A comparative analysis of the CO2 capture results and N2 porosity characterization data evidenced that the use of [Hmim][BF4], a physical solvent for carbon dioxide, ended up into a worsening of the parent AC capture performance, due to a dominating pore blocking effect at all the operating temperatures. Conversely, the less sterically-hindered and amino acid-based [Emim][Gly] IL was effective in increasing the AC capture capacity at 353 K under milder impregnation conditions, the beneficial effect being attributed to both its chemical affinity towards CO2 and low pore volume reduction. The findings derived in this work outline interesting perspectives for the application of amino acid-based IL supported onto activated carbons for CO2 separation under post-combustion conditions, and future research efforts should be focused on the search for AC characterized by optimal pore size distribution and surface properties for IL functionalization. PMID:25710387

  17. Troponin T immunosensor based on liquid crystal and silsesquioxane-supported gold nanoparticles.

    PubMed

    Zapp, Eduardo; da Silva, Paulo Sérgio; Westphal, Eduard; Gallardo, Hugo; Spinelli, Almir; Vieira, Iolanda Cruz

    2014-09-17

    A nanostructured immunosensor based on the liquid crystal (E)-1-decyl-4-[(4-decyloxyphenyl)diazenyl]pyridinium bromide (Br-Py) and gold nanoparticles supported by the water-soluble hybrid material 3-n-propyl-4-picolinium silsesquioxane chloride (AuNP-Si4Pic(+)Cl(-)) was built for the detection of troponin T (cTnT), a cardiac marker for acute myocardial infarction (AMI). The functionalized nanostructured surface was used to bind anti-cTnT monoclonal antibodies through electrostatic interaction. The immunosensor (ab-cTnT/AuNP-Si4Pic(+)Cl(-)/Br-Py/GCE) surface was characterized by microscopy techniques. The electrochemical behavior of the immunosensor was studied by cyclic voltammetry and electrochemical impedance spectroscopy. A calibration curve was obtained by square-wave voltammetry. The immnunosensor provided a limit of detection of 0.076 ng mL(-1) and a linear range between 0.1 and 0.9 ng mL(-1) (appropriate for AMI diagnosis). PMID:25111622

  18. An Efficient, Versatile, and Safe Access to Supported Metallic Nanoparticles on Porous Silicon with Ionic Liquids.

    PubMed

    Darwich, Walid; Haumesser, Paul-Henri; Santini, Catherine C; Gaillard, Frédéric

    2016-01-01

    The metallization of porous silicon (PSi) is generally realized through physical vapor deposition (PVD) or electrochemical processes using aqueous solutions. The former uses a strong vacuum and does not allow for a conformal deposition into the pores. In the latter, the water used as solvent causes oxidation of the silicon during the reduction of the salt precursors. Moreover, as PSi is hydrophobic, the metal penetration into the pores is restricted to the near-surface region. Using a solution of organometallic (OM) precursors in ionic liquid (IL), we have developed an easy and efficient way to fully metallize the pores throughout the several-µm-thick porous Si. This process affords supported metallic nanoparticles characterized by a narrow size distribution. This process is demonstrated for different metals (Pt, Pd, Cu, and Ru) and can probably be extended to other metals. Moreover, as no reducing agent is necessary (the decomposition in an argon atmosphere at 50 °C is fostered by surface silicon hydride groups borne by PSi), the safety and the cost of the process are improved. PMID:27271608

  19. Extraction of phenol using sulfuric acid salts of trioctylamine in a supported liquid membrane

    SciTech Connect

    Wang, M.L.; Hu, K.H. )

    1994-04-01

    The extraction of phenol by trioctylamine sulfate salts in a supported-liquid membrane (SLM) process was investigated. In the extraction process, a transport model, which included the film diffusion of phenol in the aqueous phase, the membrane diffusion within the SLM, and the interfacial chemical reaction, was built. The experimental parameters, such as the cell constant ([beta]), the diffusivity of (TOA)[sub 2]H[sub 2]SO[sub 4][center dot]PhOH in the SLM (D[sub c,b]), and the mass-transfer coefficient of phenol in the aqueous solution (K[sub L]), were determined from experiments. On the basis of the experimental data and the results obtained from the transport model, the rate-controlling step of the extraction of phenol by an SLM during permeation is discussed. The effects of the operating variables and parameters, such as the initial concentration of phenol in the aqueous phase, sulfuric acid, sodium hydroxide, and trioctylamine sulfate salts, on the extraction of phenol were examined.

  20. Supported liquid membrane system for Cr(III) separation from Cr(III)/Cr(VI) mixtures.

    PubMed

    Religa, P; Rajewski, J; Gierycz, P; Swietlik, R

    2014-01-01

    This paper presents the results of analyses of the chromium(III) transport process from mixtures of Cr(III)/Cr(VI) ions using supported liquid membranes (SLM), in which dinonylnaphthalene sulfonic acid (DNNSA) and di(2-ethylhexyl) phosphoric acid (D2EHPA) were used as carriers. In both cases the membrane worked as a selective barrier for Cr(VI) ions. The increase in both the time of Cr(VI) ions-carrier interaction and the Cr(VI) concentration in the feed phase negatively influenced the Cr(III) separation. The polarizing layer consisting of Cr(VI) ions prevents the access of Cr(III) ions to the inter phase surface and leads to the deactivation of the carrier, which is the result of the strong oxidation properties of Cr(VI) ions. These factors meant that, in the case of the membrane with DNNSA, the membrane could not be used for the effective separation of Cr(III) from the Cr(III)/Cr(VI) mixture. On the other hand, the membrane with D2EHPA can be used for fast and efficient transport of Cr(III) ions, but only for strictly defined process parameters, i.e. where the level of chromium(VI) concentration is below 10(-3)M and with intensive feed phase mixing. PMID:24960010

  1. Compatibility of lyotropic liquid crystals with viruses and mammalian cells that support the replication of viruses.

    PubMed

    Cheng, Li-Lin; Luk, Yan-Yeung; Murphy, Christopher J; Israel, Barbara A; Abbott, Nicholas L

    2005-12-01

    We report a study that investigates the biocompatibility of materials that form lyotropic liquid crystals (LCs) with viruses and mammalian cells that support the replication of viruses. This study is focused on aqueous solutions of tetradecyldimethyl-amineoxide (C(14)AO) and decanol (D), or disodium cromoglycate (DSCG; C(23)H(14)O(11)Na(2)), which can form optically birefringent, liquid crystalline phases. The influence of these materials on the ability of vesicular stomatitis virus (VSV) to infect human epitheloid cervical carcinoma (HeLa) cells was examined by two approaches. First, VSV was dispersed in aqueous C(14)AO+ D or DSCG, and then HeLa cells were inoculated by contacting the cells with the aqueous C(14)AO + D or DSCG containing VSV. The infectivity of VSV to the HeLa cells was subsequently determined. Second, VSV was incubated in LC phases of either C(14)AO + D or DSCG for 4 h, and the concentration (titer) of infectious virus in the LC was determined by dilution into cell culture medium and subsequent inoculation of HeLa cells. Using these approaches, we found that the LC containing C(14)AO + D caused inactivation of virus as well as cell death. In contrast, we determined that VSV retained its infectivity in the presence of aqueous DSCG, and that greater than 74-82% of the HeLa cells survived contact with aqueous DSCG (depending on concentration of DSCG). Because VSV maintained its function (and we infer structure) in LCs formed from DSCG, we further explored the influence of the virus on the ordering of the LC. Whereas the LC formed from DSCG was uniformly aligned on surfaces prepared from self-assembled monolayers (SAMs) of HS(CH(2))(11)(OCH(2)CH(2))(4)OH on obliquely deposited films of gold in the absence of VSV, the introduction of 10(7)-10(8) infectious virus particles per milliliter caused the LC to assume a non-uniform orientation and a colorful appearance that was readily distinguished from the uniformly aligned LCs. Control experiments using

  2. Selective removal and recovery of Black B reactive dye from simulated textile wastewater using the supported liquid membrane process.

    PubMed

    Harruddin, Norlisa; Othman, Norasikin; Ee Sin, Andeline Lim; Raja Sulaiman, Raja Norimie

    2015-01-01

    Effluent containing colour/dyes, especially reactive dyes, becomes a great concern of wastewater treatment because it is toxic to human life and aquatic life. In this study, reactive dye of Black B was separated using the supported liquid membrane process. Commercial polypropylene membrane was used as a support of the kerosene-tridodecylamine liquid membrane. Several parameters were tested and the result showed that almost 100% of 70 ppm Black B was removed and 99% of 70 ppm Black B was recovered at pH 2 of the feed phase containing 0.00001 M Na2SiO3, flow rate of 150 ml/min and 0.2 M NaOH. The membrane support also remained stable for up to 36 hours under an optimum condition. PMID:25514128

  3. Modeling of the mass transfer rates of metal ions across supported liquid membranes. 2: Comparison between theory and experiment

    SciTech Connect

    Elhassadi, A.A.; Do, D.D.

    1999-02-01

    The model equations developed in Part 1 were tested using experimental data reported in the literature and produced in this work. It was found that uranium(VI) and thorium(IV) can be selectively separated and concentrated using supported liquid membranes. Depending on the way the liquid membranes are designed, the selectivity toward a specific metal can be predetermined. The effect of the ratio of the effective diffusivity to bulk diffusivity in free solution was found to behave with the same characteristic of systems of preferentially adsorbed solutes.

  4. Interaction of an ionic liquid with a supported phospholipid bilayer is lipid-dependent

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Liquid salts, commonly called ionic liquids, are used as solvents to conduct transformation of vegetable oils into new products. These reactions are often catalyzed via immobilized enzymes. However, some enzymes were found to lose activity and are in need of some protection. Phospholipid bilayers...

  5. Brucella TIR-like protein TcpB/Btp1 specifically targets the host adaptor protein MAL/TIRAP to promote infection.

    PubMed

    Li, Wenna; Ke, Yuehua; Wang, Yufei; Yang, Mingjuan; Gao, Junguang; Zhan, Shaoxia; Xinying, Du; Huang, Liuyu; Li, Wenfeng; Chen, Zeliang; Li, Juan

    2016-08-26

    Brucella spp. are known to avoid host immune recognition and weaken the immune response to infection. Brucella like accomplish this by employing two clever strategies, called the stealth strategy and hijacking strategy. The TIR domain-containing protein (TcpB/Btp1) of Brucella melitensis is thought to be involved in inhibiting host NF-κB activation by binding to adaptors downstream of Toll-like receptors. However, of the five TIR domain-containing adaptors conserved in mammals, whether MyD88 or MAL, even other three adaptors, are specifically targeted by TcpB has not been identified. Here, we confirmed the effect of TcpB on B.melitensis virulence in mice and found that TcpB selectively targets MAL. By using siRNA against MAL, we found that TcpB from B.melitensis is involved in intracellular survival and that MAL affects intracellular replication of B.melitensis. Our results confirm that TcpB specifically targets MAL/TIRAP to disrupt downstream signaling pathways and promote intra-host survival of Brucella spp. PMID:27311859

  6. Microextraction of mebendazole across supported liquid membrane forced by pH gradient and electrical field.

    PubMed

    Eskandari, Mahboube; Yamini, Yadollah; Fotouhi, Lida; Seidi, Shahram

    2011-04-01

    In the present study, extraction of mebendazole across a supported-liquid membrane (SLM) was performed based on two different driving forces: (1) pH gradient over the SLM, and (2) electrical field sustained over the SLM. The extracted drug concentration was studied using reversed-phase HPLC-UV. At passive extraction conditions, mebendazole was extracted from alkaline samples (0.01 mmol L(-1) NaOH) into 1-undecanol immobilized in the pores of a porous hollow fiber of polypropylene (SLM), and then transported into 25 μL of 100mM HCl as the acceptor solution. Under electrokinetic migration conditions, mebendazole transported under applied voltage from acidic solutions (100 mmol L(-1) HCl) through 2-nitrophenyl octyl ether (NPOE) immobilized in the pores of hollow fiber, into 25 μL of 100 mmol L(-1) HCl as the acceptor solution. The effects of several factors including the nature of organic solvent, pH of donor and acceptor solutions, extraction time and stirring speed on the extraction efficiency of the drug were investigated and optimized. Under optimal conditions, preconcentration factors (PF) of 211 and 190 were obtained for the drug based on passive transport and electromembrane extraction (EME), respectively. Also, linear range of 0.5-1000 μg L(-1) with estimation of coefficient higher than 0.994 was obtained for both of the proposed methods. The results showed that EME has higher speed in comparison with simple passive transport. The methods were successfully applied to extract mebendazole from plasma and urine samples and satisfactory results were obtained. PMID:21211924

  7. Transport of chromium(VI) through a supported liquid membrane containing tri-n-octylphosphine oxide

    SciTech Connect

    Huang, T.C.; Huang, C.C.; Chen, D.H.

    1998-09-01

    In this study the transport of chromium(VI) from aqueous solutions of pH 2--4 through a supported liquid membrane (SLM) with tri-n-octylphosphine oxide (TOPO) dissolved in kerosene as a mobile carrier was investigated. The transport flux of Cr(VI) increased with an increase in the concentrations of Cr(VI) in the feed phase and of TOPO in the membrane phase, but with a decrease in pH of the feed phase. Considering the equilibria of various Cr(VI) species in the aqueous phase and of the Cr(VI)-TOPO complexes formed in the membrane phase, a permeation model including the aqueous film diffusion of HCrO{sub 4}{sup {minus}} and Cr{sub 2}O{sub 7}{sup 2{minus}} toward the membrane, the interfacial chemical reaction between them and TOPO, and the membrane diffusion of the Cr(VI)-TOPO complexes ({ovr H{sub 2}CrO{sub 4}{center_dot}(TOPO)} and {ovr H{sub 2}Cr{sub 2}O{sub 7}{center_dot}(TOPO){sub 3}}) was proposed to describe the transport of Cr(VI) through the SLM. By best fitting the transport flux equations of Cr(VI) with the experimental data using the Rosenbrock method, the apparent mass-transfer coefficients of HCrO{sub 4}{sup {minus}} and Cr{sub 2}O{sub 7}{sup 2{minus}} across the aqueous film, and those of {ovr H{sub 2}CrO{sub 4}{center_dot}(TOPO)} and {ovr H{sub 2}Cr{sub 2}O{sub 7}{center_dot}(TOPO){sub 3}} across the membrane phase, were obtained. This work helps to clarify the transport mechanism of Cr(VI) through an SLM.

  8. The behaviour of peptides on reverse-phase supports during high-pressure liquid chromatography.

    PubMed Central

    Wilson, K J; Honegger, A; Stötzel, R P; Hughes, G J

    1981-01-01

    High-pressure ('performance') liquid chromatography has been used to investigate the reverse-phase chromatographic behaviour of peptides, ranging in length from 2 to 65 amino acid residues, which have originated from primary-sequence determinations or solution/solid-phase syntheses. By using a pyridine/formate-pyridine/acetate/propan-1-ol buffer system, as previously described [Hughes, Winterhalter & Wilson (1979) FEBS Lett. 108, 81-86], the influence of various experimental parameters were examined. (a) Peptide retention was observed to be temperature-independent between 25 and 55 degrees C. (b) The dependence of chromatographic retention on pH decreases with increasing peptide hydrophobicity. (c) Chromatographic results from C8- and C18-chain-length, as well as from 5 micrometers- and 10 micrometers-particle-size, supports were comparable. (d) The hydrophobic strength of the organic solvent in the mobile phase was observed to decrease: propan-1-ol approximately equal to propan-2-ol greater than acetonitrile much greater than methanol. (e) When gradient rates (% of buffer B/unit time) were systematically decreased, peptide retention decreased in a hyperbolic manner. Comparisons of the peptides chromatographed with respect to their measured retention properties and calculated hydrophobicities were performed by computer analysis. Deviation of peptide chromatographic behaviour was observed to be essentially independent of hydrophobicity, chain length and charge. On the basis of the measured retention properties of the chromatographed peptides, hydrophobic constants for the various amino acid side chains were determined and compared with similar constants available from the literature. PMID:7337711

  9. Liquid phase methanol LaPorte Process Development Unit: Modification, operation, and support studies

    SciTech Connect

    Not Available

    1991-02-28

    The LPMEOH process was conceived and patented by Chem Systems Inc. in 1975. Initial research and studies on the process focused on two distinct modes of operation. The first was a liquid fluidized mode with relatively large catalyst pellets suspended in a fluidizing liquid, and the second was an entrained (slurry) mode with fine catalyst particles slurried in an inert liquid. The development of both operating modes progressed in parallel from bench scale reactors, through an intermediate scale lab PDU, and then to the LaPorte PDU in 1984. The slurry mode of operation was ultimately chosen as the operating mode of choice due to its superior performance.

  10. Permeation rate of metal species through supported liquid membranes: diffusional and chemical resistances with cationic and anionic carriers

    SciTech Connect

    Danesi, P.R.; Horwitz, E.P.; Rickert, P.G.

    1983-01-01

    Facilitated transport by means of a mobile carrier in an organic diluent and adsorbed on a polymeric film, through supported liquid membranes (SLM), is a new method for the separation and recovery of metal ions. A permeability coefficient equation for this transport was tested. The facilitated transport of Cu/sup 2 +/ and Fe/sup 3 +/ ions through a SLM was characterized with respect to the membrane resistance. Transport of Am/sup 3 +/ through a SLM was also characterized. (DLC)

  11. Poly(ionic liquid) complex with spontaneous micro-/mesoporosity: template-free synthesis and application as catalyst support.

    PubMed

    Zhao, Qiang; Zhang, Pengfei; Antonietti, Markus; Yuan, Jiayin

    2012-07-25

    A facile, template-free synthetic route is reported toward poly(ionic liquid) complexes (PILCs) which for the first time exhibit stable micro-/mesoporous structure. This is accomplished via in situ ionic complexation between imidazolium-based PILs and poly(acrylic acid) in various alkaline organic solvents. The PILC can be highly loaded with copper salts and can be used as a catalytic support for effective aerobic oxidation of activated hydrocarbons under mild conditions. PMID:22780888

  12. Multiresidue determination of sulfonamides in a variety of biological matrices by supported liquid membrane with high pressure liquid chromatography-electrospray mass spectrometry detection.

    PubMed

    Msagati, Titus A M; Nindi, Mathew Muzi

    2004-09-01

    A high performance liquid chromatography (HPLC) coupled to a mass spectrometer (MS) was used for a simultaneous determination of 16 sulfonamide compounds spiked in water, urine, milk, and bovine liver and kidney tissues. Supported liquid membrane (SLM) made up of 5% tri-n-octylphosphine oxide (TOPO) dissolved in hexyl amine was used as a sample clean-up and/or enrichment technique. The sulfonamides mixture was made up of 5-sulfaminouracil, sulfaguanidine, sulfamethoxazole, sulfamerazine, sulfamethizole, sulfamethazine (sulfadimidine), sulfacetamide, sulfapyridine, sulfabenzamide, sulfamethoxypyridazine, sulfamonomethoxine, sulfadimethoxine sulfasalazine, sulfaquinoxaline, sulfadiazine, and sulfathiazole. Some of these compounds, such as, sulfaquinoxaline, sulfadiazine, sulfabenzamide, sulfathiazole and sulfapyridine failed to be trapped efficiently by the same liquid membrane (5% TOPO in hexylamine). The detection limits (DL) obtained were 1.8ppb for sulfaguanidine and sulfamerazine and between 3.3 and 10ppb in bovine liver and kidney tissues for the other sulfonamides that were successfully enriched with SLM; 2.1ppb for sulfaguanidine and sulfamerazine and between 7.5 and 15ppb in cow's urine, whereas the DL values in milk were 12.4ppb for sulfaguanidine and sulfamerazine and between 16.8 and 24.3 for the other compounds that were successfully enriched by the membrane. Several factors affecting the extraction efficiency during SLM enrichment, such as donor pH, acceptor pH, enrichment time and the membrane solvent were studied. PMID:18969572

  13. Polymeric ionic liquid and carbon black composite as a reusable supporting electrolyte: modification of the electrode surface.

    PubMed

    Yoo, Seung Joon; Li, Long-Ji; Zeng, Cheng-Chu; Little, R Daniel

    2015-03-16

    One of the major impediments to using electroorganic synthesis is the need for large amounts of a supporting electrolyte to ensure the passage of charge. Frequently this causes separation and waste problems. To address these issues, a polymeric ionic liquid-Super P carbon black composite has been formulated. The system enables electrolyses to be performed without adding an additional supporting electrolyte, and its efficient recovery and reuse. In addition, the ability of the composite to modify the electrode surface in situ leads to improved kinetics. A practical consequence is that one can decrease catalyst loading without sacrificing efficiency. PMID:25619992

  14. Urine sample preparation of tricyclic antidepressants by means of a supported liquid membrane technique for high-performance liquid chromatographic analysis.

    PubMed

    Trocewicz, J

    2004-03-01

    Supported liquid membrane (SLM) technique for sample work-up and enrichment was used for determination of tricyclic antidepressant drugs in urine by high-performance liquid chromatography (HPLC) with UV detection. The studied antidepressant drugs were amitriptyline, opipramol, noxiptyline and additionally diethazine was used as possible internal standard. Alkaline phosphoric buffer with urine sample, as the donor solution, was passed over the liquid membrane into which investigated substances were extracted. On the other side of the membrane, analyzed compounds were trapped due to creating non-extractable form in acidic acceptor solution. Enriched and cleaned up drugs were then injected into a HPLC system with ultraviolet detection to analyze of their concentration in acceptor solution. Optimum extraction efficiency was determined by changing acceptor and donor solutions pH, application of different flow rates of donor solution and by using different solvents in the membrane. Also, donor solution volume, extraction time and concentration of analytes were varied to check the linearity of extraction process. The highest extraction efficiency: 43% for opipramol, 56% for noxiptyline, 43% for amitriptyline and 42% for diethazine (R.S.D. values were <6% and n=3) was achieved when 0.05 M phosphate buffer pH 4.0 and 9.5 were used as donor and acceptor solutions, respectively, n-undecane with 5% tri-n-octylphosphine oxide (TOPO) was used as liquid membrane. Limit of quantification (LOQ) for tricyclic antidepressants after enrichment of 100ml of urine sample was about 1 ng/ml. PMID:14751789

  15. Interaction of a microsphere with a solid-supported liquid film.

    PubMed

    Ally, Javed; Vittorias, Ewa; Amirfazli, A; Kappl, Michael; Bonaccurso, Elmar; McNamee, Cathy E; Butt, Hans-Jürgen

    2010-07-20

    The interaction between particles with thin liquid films on solid surfaces was studied by sintering polystyrene microspheres of 4 to 5 microm diameter to the end of atomic force microscope cantilevers. Films of three silicone oils (viscosity 4.6, 9.2, and 9700 mPa s) and water of thickness 0.2-1.8 microm were formed on glass. The interaction between a particle and the film was measured at different particle approach/retraction velocities. The interaction is dominated by capillary and hydrodynamic forces. It depends on the surface tension and the viscosity of the liquid. The film thickness can be determined from the force curves. In addition, the meniscus formation of a film wetting a particle was demonstrated experimentally by solidifying a liquid polystyrene film as it wetted glass particles. PMID:20568819

  16. A promising method of liquid separation in orbital station's life support systems

    NASA Astrophysics Data System (ADS)

    Kapitsa Anna, A.

    2012-11-01

    A combined method of liquid separation from a gas-liquid flow is presented based on an analysis of existing methods of separation and experience gained from the Russian space stations Salut, Mir and the International Space Station. This method combines the advantages of both water-holding materials and semi-permeable membranes. The paper describes an actual device as well as laboratory test results for materials and the separator. The separator described has successfully been in experimental operation on the ISS since the 1st of September 2009.

  17. Piping support system for liquid-metal fast-breeder reactor

    DOEpatents

    Brussalis, Jr., William G.

    1984-01-01

    A pipe support consisting of a rigid link pivotally attached to a pipe and an anchor, adapted to generate stress or strain in the link and pipe due to pipe thermal movement, which stress or strain can oppose further pipe movement and generally provides pipe support. The pipe support can be used in multiple combinations with other pipe supports to form a support system. This support system is most useful in applications in which the pipe is normally operated at a constant elevated or depressed temperature such that desired stress or strain can be planned in advance of pipe and support installation. The support system is therefore especially useful in steam stations and in refrigeration equipment.

  18. Monitoring of N-methyl carbamate pesticide residues in water using hollow fibre supported liquid membrane and solid phase extraction

    NASA Astrophysics Data System (ADS)

    Msagati, Titus A. M.; Mamba, Bhekie B.

    The aim of this work was to develop a method for the determination of N-methyl carbamates in water involving hollow fibre supported liquid membrane (HFSLM) and solid phase extraction (SPE) as sample preparation methods. Four N-methyl carbamate pesticides, aldicarb, carbaryl, carbofuran and methiocarb sulfoxide, were simultaneously extracted and analysed by a liquid chromatograph with a diode array detector (LC-UV/DAD) and a liquid chromatograph coupled to a ion trap quadrupole mass spectrometer (LC-ESI-MS). The high performance liquid chromatography (HPLC) separation of carabamate extracts was performed on a C18 column with water-acetonitrile as the mobile phase. The mass spectrometry analyses were carried out in the positive mode, operating under both the selected ion monitoring (SIM) and full scan modes. The solid phase recoveries of the extracts ranged between 8% and 98%, with aldicarb having the highest recoveries, followed by carbaryl, carbofuran and methiocarb had the lowest recovery. The HFSLM recovery ranged between 8% and 58% and the order of recovery was similar to the SPE trend. Factors controlling the efficiency of the HFSLM extraction such as sample pH, stripping phase pH, enrichment time, stirring speed as well as organic solvent used for entrapment of analytes, were optimised to achieve the highest enrichment factors.

  19. Buildings R&D Breakthroughs: Technologies and Products Supported by the Building Technologies Program

    SciTech Connect

    Weakley, Steven A.

    2012-04-15

    The purpose of the project described in this report is to identify and characterize commercially available products and emerging (near-commercial) technologies that benefited from the support of the Building Technologies Program (BTP) within the U.S. Department of Energy’s Office of Energy Efficiency and Renewable Energy. The investigation specifically focused on technology-oriented research and development (R&D) projects funded by BTP’s Emerging Technologies subprogram from 2005-2011.

  20. Buildings R&D Breakthroughs. Technologies and Products Supported by the Building Technologies Program

    SciTech Connect

    none,

    2012-04-01

    This report identifies and characterizes commercially available products and emerging (near-commercial) technologies that benefited from the support of the Building Technologies Program (BTP) within the U.S. Department of Energy’s Office of Energy Efficiency and Renewable Energy. The investigation specifically focused on technology-oriented research and development (R&D) projects sponsored by BTP’s Emerging Technologies subprogram from 2005-2009.

  1. Effects of Silica Nanoparticle Supported Ionic Liquid as Additive on Thermal Reversibility of Human Carbonic Anhydrase II

    PubMed Central

    Fallahbagheri, Azadeh; Saboury, Ali Akbar; Ma'mani, Leila; Taghizadeh, Mohammad; Khodarahmi, Reza; Ranjbar, Samira; Bohlooli, Mousa; Shafiee, Abbas; Foroumadi, Alireza; Sheibani, Nader; Moosavi-Movahedi, Ali Akbar

    2013-01-01

    Silica nanoparticle supported imidazolium ionic liquid [SNImIL] was synthesized and utilized as a biocompatible additive for studying the thermal reversibility of human carbonic anhydrase II (HCA II). For this purpose, we prepared additive by modification of nanoparticles through the grafting of ionic liquids on the surface of nanoparticles (SNImIL). The SNImIL were fully characterized by Fourier Transform Infrared spectroscopy, scanning electron microscopy and thermo gravimetric analysis. The characterization of HCA II was investigated by various techniques including UV–Vis and ANS fluorescence spectrophotometry, differential scanning calorimetry, and docking study. SNImIL induced disaggregation, enhanced protein stability and increased thermal reversibility of HCA II by up to 42% at pH 7.75. PMID:22829053

  2. Hollow fiber-supported designer ionic liquid sponges for post-combustion CO2 scrubbing

    SciTech Connect

    Lee, JS; Hillesheim, PC; Huang, DK; Lively, RP; Oh, KH; Dai, S; Koros, WJ

    2012-11-30

    A proof of concept study for a new type of carbon capture system is considered for post-combustion CO2 capture based on porous hollow fiber sorbents with ionic liquids sorbed in the cell walls of the fiber. This study proves that delicate morphological features in the open-celled porous wall can be maintained during the infusion process. Mixtures of task specific ionic liquid (i.e. [BMIM][Tf2N]) and superbase (i.e. DBU) were loaded into polyamide-imide (PAI) fibers by a so-called two-step non-solvent infusion protocol. In the protocol, methanol carries ionic liquids into the pore cell walls of hollow fibers and then hexane carries superbase to create an efficient CO2 sorbent. Our ionic liquid/superbase impregnation technique overcomes a serious increase in mass transfer resistance upon reaction with CO2, thereby allowing its large scale utilization for post-combustion CO2 capture. The investigation on the effect of different pore former additives (different molecular weights of polyvinylpyrrolidone, lithium nitrate, and their mixtures) suggested that a large molecular weight of PVP (M-w; 1300k) including dope composition produces highly interconnected open cell pore structures of PAI hollow fibers. Lastly, a lumen side barrier layer was successfully formed on the bore side of neat PAI fibers by using a mixture of Neoprene (R) with crosslinking agents (TSR-633) via a post-treatment process. The lumen layer will enable heat removal from the fiber sorbents during their application in rapid thermal swing cycling processes. (C) 2012 Elsevier Ltd. All rights reserved.

  3. Determination of chemotherapeutic drugs in human urine by capillary electrophoresis with UV and fluorimetric detection using solid-supported liquid-liquid extraction for sample clean-up.

    PubMed

    Hurtado-Sánchez, María del Carmen; Acedo-Valenzuela, María Isabel; Durán-Merás, Isabel; Rodríguez-Cáceres, María Isabel

    2015-06-01

    Capillary electrophoresis was used for the rapid determination of three chemotherapeutic drugs employed to treat colorectal cancer: irinotecan, tegafur, and leucovorin, and their main metabolites (7-ethyl-10-hydroxycamptothecin and 5-fluorouracil), in human urine samples. A phosphate buffer (pH 11.34; 20 mM) was selected as the background electrolyte. A hydrodynamic injection (9 s, 30 mbar) was applied and the separation was carried out using a separation temperature and voltage of 25°C and 25 kV, respectively. A capillary with two detection windows for serial online UV and fluorescence detection was satisfactorily employed. A solid-supported liquid-liquid extraction procedure was optimized for the clean-up of the urine samples and the extraction of the analytes. Matrix effects were assessed and signal suppression was observed for three of the analytes, thus, matrix-matched calibration was used for compensating residual matrix effects on these analytes. The proposed method allows the separation and quantification of the chemotherapeutics in less than 6 min. Detection limits range between 0.01 and 0.30 mg/L. The method was satisfactorily applied to the determination of the target compounds in human urine samples, with recoveries of 92.4-107.7%. PMID:25820908

  4. Simultaneous determination of polycyclic musks in blood and urine by solid supported liquid-liquid extraction and gas chromatography-tandem mass spectrometry.

    PubMed

    Liu, Hongtao; Huang, Liping; Chen, Yuxin; Guo, Liman; Li, Limin; Zhou, Haiyun; Luan, Tiangang

    2015-06-15

    A rapid, precise and accurate method for the simultaneous determination of 5 polycyclic musks (PCMs) in biological fluids was developed by solid supported liquid-liquid extraction (SLE) coupled with gas chromatography-tandem mass spectrometry (GC-MS/MS). All parameters influencing SLE-GC-MS performance, including electron energy of electron-impact ionization source, collision energy for tandem mass spectrometer when operated in selected-reaction monitoring (SRM) mode, type and volume of elution reagent, nitrogen evaporation time, pH and salinity of sample have been carefully optimized. Eight milliliter of n-hexane was finally chosen as elution reagent. Blood and urine sample could be loaded into SLE cartridge without adjusting pH and salinity. Deuterated tonalide (AHTN-d3) was chosen as internal standard. The correlation coefficient (r(2)) of the calibration curves of target compounds ranged from 0.9996 to 0.9998. The dynamic range spanned over two orders of magnitude. The limit of detection (LOD) of target compounds in blood and urine ranged from 0.008 to 0.105μgL(-1) and 0.005 to 0.075μgL(-1), respectively. The developed procedure was successfully applied to the analysis of PCMs in human blood and urine obtaining satisfying recoveries on low, medium and high levels. The method was compared with SLE-GC-MS and shown one to two orders of magnitude improvement in sensitivity. PMID:25965876

  5. Determination of ketamine, norketamine and dehydronorketamine in urine by hollow-fiber liquid-phase microextraction using an essential oil as supported liquid membrane.

    PubMed

    Bairros, André Valle de; Lanaro, Rafael; Almeida, Rafael Menck de; Yonamine, Mauricio

    2014-10-01

    Here, we present a method for the determination of ketamine (KT) and its main metabolites, norketamine (NK) and dehydronorketamine (DHNK) in urine samples by using hollow-fiber liquid-phase microextraction (HF-LPME) in the three-phase mode. The fiber pores were filled with eucalyptus essential oil and a solution of 1.0mol/L of HCl was introduced into the lumen of the fiber (acceptor phase). The fiber was submersed in the alkalinized urine containing 10% NaCl, and the system was submitted to lateral shaking (2400rpm) during 30min. Acceptor phase was withdrawn from the fiber, dried and the residue was then derivatized with trifluoroacetic anhydride (TFAA) for further determination by gas chromatography-mass spectrometry (GC-MS). The calibration curves were linear over the specified range and limits of detection (LoDs) obtained for KT, NK and DHNK were below the cut-off value (1.0ng/mL) recommended by the United Nations Office on Drugs and Crime (UNODC). A totally "green chemistry" approach of the sample extraction was obtained by using essential oil as a supported liquid membrane in HF-LPME. The developed method was successfully validated and applied to urine samples collected from two clinical cases in which KT was suspected to be involved. PMID:24810678

  6. Thermo-mechanical simulation of liquid-supported stretch blow molding

    SciTech Connect

    Zimmer, J.; Stommel, M.

    2015-05-22

    Stretch blow molding is the well-established plastics forming method to produce Polyehtylene therephtalate (PET) bottles. An injection molded preform is heated up above the PET glass transition temperature (Tg∼85°C) and subsequently inflated by pressurized air into a closed cavity. In the follow-up filling process, the resulting bottle is filled with the final product. A recently developed modification of the process combines the blowing and filling stages by directly using the final liquid product to inflate the preform. In a previously published paper, a mechanical simulation and successful evaluation of this liquid-driven stretch blow molding process was presented. In this way, a realistic process parameter dependent simulation of the preform deformation throughout the forming process was enabled, whereas the preform temperature evolution during forming was neglected. However, the formability of the preform is highly reduced when the temperature sinks below Tg during forming. Experimental investigations show temperature-induced failure cases due to the fast heat transfer between hot preform and cold liquid. Therefore, in this paper, a process dependent simulation of the temperature evolution during processing to avoid preform failure is presented. For this purpose, the previously developed mechanical model is used to extract the time dependent thickness evolution. This information serves as input for the heat transfer simulation. The required material parameters are calibrated from preform cooling experiments recorded with an infrared-camera. Furthermore, the high deformation ratios during processing lead to strain induced crystallization. This exothermal reaction is included into the simulation by extracting data from preform measurements at different stages of deformation via Differential Scanning Calorimetry (DSC). Finally, the thermal simulation model is evaluated by free forming experiments, recorded by a high-speed infrared camera.

  7. Thermo-mechanical simulation of liquid-supported stretch blow molding

    NASA Astrophysics Data System (ADS)

    Zimmer, J.; Stommel, M.

    2015-05-01

    Stretch blow molding is the well-established plastics forming method to produce Polyehtylene therephtalate (PET) bottles. An injection molded preform is heated up above the PET glass transition temperature (Tg˜85°C) and subsequently inflated by pressurized air into a closed cavity. In the follow-up filling process, the resulting bottle is filled with the final product. A recently developed modification of the process combines the blowing and filling stages by directly using the final liquid product to inflate the preform. In a previously published paper, a mechanical simulation and successful evaluation of this liquid-driven stretch blow molding process was presented. In this way, a realistic process parameter dependent simulation of the preform deformation throughout the forming process was enabled, whereas the preform temperature evolution during forming was neglected. However, the formability of the preform is highly reduced when the temperature sinks below Tg during forming. Experimental investigations show temperature-induced failure cases due to the fast heat transfer between hot preform and cold liquid. Therefore, in this paper, a process dependent simulation of the temperature evolution during processing to avoid preform failure is presented. For this purpose, the previously developed mechanical model is used to extract the time dependent thickness evolution. This information serves as input for the heat transfer simulation. The required material parameters are calibrated from preform cooling experiments recorded with an infrared-camera. Furthermore, the high deformation ratios during processing lead to strain induced crystallization. This exothermal reaction is included into the simulation by extracting data from preform measurements at different stages of deformation via Differential Scanning Calorimetry (DSC). Finally, the thermal simulation model is evaluated by free forming experiments, recorded by a high-speed infrared camera.

  8. Liquid phase methanol LaPorte process development unit: Modification, operation, and support studies

    SciTech Connect

    Not Available

    1991-01-02

    Liquid-entrained operations at the LaPorte Liquid Phase Methanol (LPMEOH) Process Development Unit (PDU) continued during June and July 1988 under Tasks 2.1 and 2.2 of Contract No. DE-AC22-87PC90005 for the US Department of Energy. The primary focus of this PDU operating program was to prepare for a confident move to the next scale of operation with an optimized and simplified process. Several new design options had been identified and thoroughly evaluated in a detailed process engineering study completed under the LPMEOH Part-2 contract (DE-AC22-85PC80007), which then became the basis for the current PDU modification/operating program. The focus of the Process Engineering Design was to optimize and simplifications focused on the slurry loop, which consists of the reactor, vapor/liquid separator, slurry heat exchanger, and slurry circulation pump. Two-Phase Gas Holdup tests began at LaPorte in June 1988 with nitrogen/oil and CO- rich gas/oil systems. The purpose of these tests was to study the hydrodynamics of the reactor, detect metal carbonyl catalyst poisons, and train operating personnel. Any effect of the new gas sparger and the internal heat exchanger would be revealed by comparing the hydrodynamic data with previous PDU hydrodynamic data. The Equipment Evaluation'' Run E-5 was conducted at the LaPorte LPMEOH PDU in July 1988. The objective of Run E-5 was to systematically evaluate each new piece of equipment (sparger, internal heat exchanger, V/L disengagement zone, demister, and cyclone) which had been added to the system, and attempt to run the reactor in an internal-only mode. In addition, a successful catalyst activation with a concentrated (45 wt % oxide) slurry was sought. 9 refs., 26 figs., 15 tabs.

  9. A rope-net support system for the liquid scintillator detector for the SNO+ experiment

    NASA Astrophysics Data System (ADS)

    Bialek, A.; Chen, M.; Cleveland, B.; Gorel, P.; Hallin, A.; Harvey, P. J.; Heise, J.; Kraus, C.; Krauss, C. B.; Lawson, I.; Ng, C. J.; Pinkney, B.; Rogowsky, D. M.; Sibley, L.; Soluk, R.; Soukup, J.; Vázquez-Jáuregui, E.

    2016-08-01

    The detector for the SNO+ experiment consists of 780 000 kg of liquid scintillator contained in an acrylic vessel that is surrounded by water. A mechanical system has been installed to counteract the 1.25 MN of buoyant force on the acrylic and prevent the vessel from moving. The system is a rope net, designed using a Finite Element Analysis to calculate the amount of stress on the acrylic induced by the ropes, hydrostatic pressures and gravity. A dedicated test was performed to measure strains in the acrylic arising from the complex geometry of the knots in the rope system. The ratio between measured and FEA calculated strains was 1.3.

  10. Status of development and licensing support for advanced liquid metal reactors in the United States

    SciTech Connect

    Pedersen, D.R. ); Gyorey, G. )

    1991-01-01

    The cornerstones of the United States Advanced Liquid Metal Cooled Reactor (ALMR) program sponsored by the Department of Energy are: the ALMR plant design program at General Electric based on the PRISM (Power Reactor Innovative Small Module) concept, and the Integral Fast Reactor program (IFR) at Argonne National Laboratory (ANL). The goal of the US program is to produce a standard, commercial ALMR, including the associated fuel cycle. The paper addresses the status of the IFR program, the ALMR program and the interaction of the ALMR program with the regulatory environment.

  11. Status of development and licensing support for advanced liquid metal reactors in the United States

    SciTech Connect

    Pedersen, D.R.; Gyorey, G.

    1991-12-01

    The cornerstones of the United States Advanced Liquid Metal Cooled Reactor (ALMR) program sponsored by the Department of Energy are: the ALMR plant design program at General Electric based on the PRISM (Power Reactor Innovative Small Module) concept, and the Integral Fast Reactor program (IFR) at Argonne National Laboratory (ANL). The goal of the US program is to produce a standard, commercial ALMR, including the associated fuel cycle. The paper addresses the status of the IFR program, the ALMR program and the interaction of the ALMR program with the regulatory environment.

  12. Homeotropic alignment and director structures in thin films of triphenylamine-based discotic liquid crystals controlled by supporting nanostructured substrates and surface confinement.

    PubMed

    Choudhury, Trirup Dutta; Rao, Nandiraju V S; Tenent, Robert; Blackburn, Jeffrey; Gregg, Brian; Smalyukh, Ivan I

    2011-02-01

    We explore the effects of nanoscale morphology of supporting solid substrates on alignment, defects, and director structures exhibited by thin films of triphenylamine-based discotic liquid crystals. Fluorescence confocal polarizing microscopy and intrinsic polarized fluorescence properties of studied molecules are used to visualize three-dimensional director fields in the liquid crystal films. We demonstrate that, by controlling surface anchoring on supporting or confining solid substrates such as those of carbon nanotube electrodes on glass plates, both uniform homeotropic and in-plane (edge-on) alignment and nonuniform structures with developable domains can be achieved for the same discotic liquid crystal material. PMID:21214228

  13. Apparatus for supporting contactors used in extracting nuclear materials from liquids

    DOEpatents

    Leonard, Ralph A.; Frank, Robert C.

    1991-01-01

    Apparatus is provided for supporting one or more contactor stages used to remove radioactive materials from aqueous solutions. The contactor stages include a housing having an internal rotor, a motor secured to the top of the housing for rotating the rotor, and a drain in the bottom of the housing. The support apparatus includes two or more vertical members each secured to a ground support that is horizontal and perpendicular to the frame member, and a horizontally disposed frame member. The frame member may be any suitable shape, but is preferably a rectangular tube having substantially flat, spaced top and bottom surfaces separated by substantially vertical side surfaces. The top and bottom surfaces each have an opening through which the contactor housing is secured so that the motor is above the frame and the drain is below the frame during use.

  14. HELP (high efficiency liquid phase) new oligonucleotide synthesis on soluble polymeric support.

    PubMed

    Bonora, G M; Scremin, C L; Colonna, F P; Garbesi, A

    1990-06-11

    A simple, rapid and high-yielding method for the synthesis of oligonucleotides by the phosphotriesters approach is described. The use of polyethylene glycol (PEG) as soluble polymeric support preserves some convenient features of the solid-phase synthesis with new interesting advantages. Short oligonucleotides in hundred milligrams scale can be obtained from few grams of functionalized PEG. PMID:2356115

  15. HELP (high efficiency liquid phase) new oligonucleotide synthesis on soluble polymeric support.

    PubMed Central

    Bonora, G M; Scremin, C L; Colonna, F P; Garbesi, A

    1990-01-01

    A simple, rapid and high-yielding method for the synthesis of oligonucleotides by the phosphotriesters approach is described. The use of polyethylene glycol (PEG) as soluble polymeric support preserves some convenient features of the solid-phase synthesis with new interesting advantages. Short oligonucleotides in hundred milligrams scale can be obtained from few grams of functionalized PEG. PMID:2356115

  16. Dynamic study of nanodroplet nucleation and growth on self-supported nanothick liquid films.

    PubMed

    Barkay, Z

    2010-12-01

    The dynamics of water condensation on self-supported thin films was studied at the nanoscale using transmitted electrons in an environmental scanning electron microscope. The initial stages of nucleation and growth over nanothick water films have been investigated. Irregularities at the water-film boundaries constituted nucleation sites for asymmetric dropwise and filmwise condensation. Nanodroplet growth was associated with center of mass movement, and the dynamic growth power law dependence was explored for the nanoscale. PMID:21073155

  17. Liquid phase methanol LaPorte process development unit: Modification, operation, and support studies

    SciTech Connect

    Not Available

    1990-10-23

    The objectives of this program are to implement and test the process improvements identified through the engineering studies of the current program to demonstrate the capability of long-term catalyst activity maintenance, and to perform process and design engineering work that can be applied to a scaled-up Liquid Phase Methanol (LPMEOH) facility. An optional series of PDU runs is offered to extend the testing of the process improvements. A parallel research program will be performed to enhance the LPMEOH technical data base to improve the likelihood of commercialization of the LPMEOH process. Activities this quarter include: Flow sheet development for La Porte PDU modifications continues. A preliminary P ID review was completed and flow sheet modifications were identified and are being incorporated. A preliminary hazards review was completed on 22 May. Some minor flow sheet modifications resulted and a number of action items were identified. The most significant action item is to develop a materials reactivity and compatibility grid for the different alcohols, ethers, and esters which will be produced at the PDU. Heat and material balances were completed for the maximum production case of the mixed DME/MEOH synthesis campaign. An improved rate expression was developed. 1 fig.

  18. Designing Supported Ionic Liquids (ILs) within Inorganic Nanosheets for CO₂ Capture Applications.

    PubMed

    Zhou, Yingjie; Liu, Jingjing; Xiao, Min; Meng, Yuezhong; Sun, Luyi

    2016-03-01

    A new methodology was developed for the immobilization of ionic liquids (ILs) on α-zirconium phosphate (ZrP) and montmorillonite (MMT) single-layer nanosheets via a facile coassembly process. The coassembled inorganic nanosheet/1-n-butyl-3-methylimidazolium chloride (BMIMCl) hybrids were systematically characterized. The results showed that the ILs were successfully assembled with ZrP or MMT single-layer nanosheets to form an intercalated structure. The inorganic nanosheet/IL hybrids can serve as efficient CO2 absorbents. The CO2 sorption of BMIMCl could be made up to 21 times more efficient because of the high exposure of the functional groups of BMIMCl in the coassembled hybrids. CO2 was physically absorbed by the hybrids with a slow equilibrium time at lower temperatures, whereas higher temperatures allowed for faster diffusion and chemical absorption of CO2. The best CO2 capture capacities of the hybrids were 0.73 mmol/g at 60 °C for ZrP/BMIMCl and 0.42 mmol/g at 70 °C for MMT/BMIMCl. PMID:26840623

  19. Liquid phase methanol LaPorte process development unit: Modification operation, and support studies

    SciTech Connect

    Not Available

    1991-01-28

    In April 1987, Air Products started the third and final contract with the US Department of Energy to develop the Liquid Phase Methanol (LPMEOH) process. One of the objectives was to identify alternative commercial catalyst(s) for the process. This objective was strategically important as we want to demonstrate that the LPMEOH process is flexible and not catalyst selection limited. Among three commercially available catalysts evaluated in the lab, the catalyst with a designation of F21/0E75-43 was the most promising candidate. The initial judging criteria included not only the intrinsic catalyst activity but also the ability to be used effectively in a slurry reactor. The catalyst was then advanced for a 40-day life test in a laboratory 300 cc autoclave. The life test result also revealed superior stability when compared with that of a standard catalyst. Consequently, the new catalyst was recommended for demonstration in the Process Development Unit (PDU) at LaPorte, Texas. This report details the methodology of testing and selecting the catalyst.

  20. Highly dispersed ruthenium hydroxide supported on titanium oxide effective for liquid-phase hydrogen-transfer reactions.

    PubMed

    Yamaguchi, Kazuya; Koike, Takeshi; Kim, Jung Won; Ogasawara, Yoshiyuki; Mizuno, Noritaka

    2008-01-01

    Supported ruthenium hydroxide catalysts (Ru(OH)(x)/support) were prepared with three different TiO(2) supports (anatase TiO(2) (TiO(2)(A), BET surface area: 316 m(2) g(-1)), anatase TiO(2) (TiO(2)(B), 73 m(2) g(-1)), and rutile TiO(2) (TiO(2)(C), 3.2 m(2) g(-1))), as well as an Al(2)O(3) support (160 m(2) g(-1)). Characterizations with X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), electron spin resonance (ESR), and X-ray absorption fine structure (XAFS) showed the presence of monomeric ruthenium(III) hydroxide and polymeric ruthenium(III) hydroxide species. Judging from the coordination numbers of the nearest-neighbor Ru atoms and the intensities of the ESR signals, the amount of monomeric hydroxide species increased in the order of Ru(OH)(x)supported ruthenium hydroxide catalysts, especially Ru(OH)(x)/TiO(2)(A), showed high catalytic activities and selectivities for liquid-phase hydrogen-transfer reactions, such as racemization of chiral secondary alcohols and the reduction of carbonyl compounds and allylic alcohols. The catalytic activities of Ru(OH)(x)/TiO(2)(A) for these hydrogen-transfer reactions were at least one order of magnitude higher than those of previously reported heterogeneous catalysts, such as Ru(OH)(x)/Al(2)O(3). These catalyses were truly heterogeneous, and the catalysts recovered after the reactions could be reused several times without loss of catalytic performance. The reaction rates monotonically increased with an increase in the amount of monomeric ruthenium hydroxide species, which suggests that the monomeric species are effective for these hydrogen-transfer reactions. PMID:19021181

  1. Liquid Phase Methanol LaPorte Process Development Unit: Modification, operation, and support studies

    SciTech Connect

    Not Available

    1990-08-31

    A gas phase and a slurry phase radioactive tracer study was performed on the 12 ton/day Liquid Phase Methanol (LPMEOH) Process Development Unit (PDU) in LaPorte, Texas. To study the gas phase mixing characteristics, a radioactive argon tracer was injected into the feed gas and residence time distribution was generated by measuring the response at the reactor outlet. Radioactive manganese oxide powder was independently injected into the reactor to measure the slurry phase mixing characteristics. A tanks-in-series model and an axial dispersion model were applied to the data to characterize the mixing in the reactor. From the axial dispersion model, a translation to the number of CSTR's (continuous stirred tank reactors) was made for comparison purposes with the first analysis. Dispersion correlations currently available in the literature were also compared. The tanks-in-series analysis is a simpler model whose results are easily interpreted. However, it does have a few drawbacks; among them, the lack of a reliable method for scaleup of a reactor and no direct correlation between mixing in the slurry and gas phases. The dispersion model allows the mixing in the gas and slurry phases to be characterized separately while including the effects of phase transfer. This analysis offers a means for combining the gas and slurry phase dispersion models into an effective dispersion coefficient, which, in turn, can be related to an equivalent number of tanks-in-series. The dispersion methods reported are recommended for scaleup of a reactor system. 24 refs., 18 figs., 8 tabs.

  2. CMOS VLSI pilot and support chip for a liquid crystal on silicon 8x8 optical cross connect

    NASA Astrophysics Data System (ADS)

    Lelah, Alan; Vinouze, Bruno; Martel, Gilbert; Perez-Segovia, Tomas; Geoffroy, Philippe; Laval, Jean-Paul; Jayet, Philippe; Senn, Patrice; Gravey, Philippe; Wolffer, Nicole; Lever, Roger; Tan, Antione

    2001-12-01

    With the explosion of Internet and multi-service traffic, telecommunication transport networks today are turning to Wavelength Division Multiplexing. Optical cross-connects (OXCs) allow flexible rerouting of wavelength channels. It has been shown that 2-D free-space beam deflection by nematic liquid crystal gratings provide a good solution for the realization of optical switches in OXCs. Operating in the telecom 1.5 micrometers wavelength region they serve as an active holographic element. Liquid Crystal on Silicon (LCOS) combined with VLSI technologies allow the fabrication of large capacity, low cost and low consumption compact free-space switches. An N X N optical switch can be built by cascading two LCOS-based spatial light modulators (SLMs). The first part of the paper describes a circuit that provides the physical support as well as piloting circuitry for such SLMs. It is capable of piloting beams from a linear array of 8 incoming fibers towards a similar array of 8 outgoing fibers. The electrode command voltages are analog while the external interface as well as on-chip memory is digital. The chip has been implemented in a CMOS 0.5 (mu) process with 600,000 transistors while die size is 320 mm2 (80 mm2 active area).

  3. Unlocking the potential of supported liquid phase catalysts with supercritical fluids: low temperature continuous flow catalysis with integrated product separation

    PubMed Central

    Franciò, Giancarlo; Hintermair, Ulrich; Leitner, Walter

    2015-01-01

    Solution-phase catalysis using molecular transition metal complexes is an extremely powerful tool for chemical synthesis and a key technology for sustainable manufacturing. However, as the reaction complexity and thermal sensitivity of the catalytic system increase, engineering challenges associated with product separation and catalyst recovery can override the value of the product. This persistent downstream issue often renders industrial exploitation of homogeneous catalysis uneconomical despite impressive batch performance of the catalyst. In this regard, continuous-flow systems that allow steady-state homogeneous turnover in a stationary liquid phase while at the same time effecting integrated product separation at mild process temperatures represent a particularly attractive scenario. While continuous-flow processing is a standard procedure for large volume manufacturing, capitalizing on its potential in the realm of the molecular complexity of organic synthesis is still an emerging area that requires innovative solutions. Here we highlight some recent developments which have succeeded in realizing such systems by the combination of near- and supercritical fluids with homogeneous catalysts in supported liquid phases. The cases discussed exemplify how all three levels of continuous-flow homogeneous catalysis (catalyst system, separation strategy, process scheme) must be matched to locate viable process conditions. PMID:26574523

  4. A review of the supply of liquid propellants and other fluids in support of the Space Shuttle Program

    NASA Technical Reports Server (NTRS)

    Churchwell, Stacy E.; Bain, A. L.

    1989-01-01

    In this study, over twenty significant liquid propellants and other fluids were reviewed as to their supply in support of the Space Shuttle Program (SSP), primarily at KSC. The uniqueness of most of the products, either by their application or production characteristics, present a variety of supply issues to contend with. Each, however, is critical to the success of the SSP. It becomes necessary to formulate, and maintain, a logistic approach to assure a continued availability of each product. For convenience, two categories were established. One, labeled limited-availability, represents those products wherein they are single sourced, have production restrictions and/or there has been a history of supply problems. The other, labeled universally-available, is characteristic of those having several sources and/or having little, if any, historical supply problems. This last category was not examined in depth. Through concepts of establishing stockpile inventories, multiple supply contracts, or other arrangements, the supply of liquid propellants and other fluids can be assured.

  5. MAGNETIC LIQUID DEFORMABLE MIRRORS FOR ASTRONOMICAL APPLICATIONS: ACTIVE CORRECTION OF OPTICAL ABERRATIONS FROM LOWER-GRADE OPTICS AND SUPPORT SYSTEM

    SciTech Connect

    Borra, E. F.

    2012-08-01

    Deformable mirrors are increasingly used in astronomy. However, they still are limited in stroke for active correction of high-amplitude optical aberrations. Magnetic liquid deformable mirrors (MLDMs) are a new technology that has the advantages of high-amplitude deformations and low costs. In this paper, we demonstrate extremely high strokes and interactuator strokes achievable by MLDMs which can be used in astronomical instrumentation. In particular, we consider the use of such a mirror to suggest an interesting application for the next generation of large telescopes. We present a prototype 91 actuator deformable mirror made of a magnetic liquid (ferrofluid). This mirror uses a technique that linearizes the response of such mirrors by superimposing a large and uniform magnetic field on the magnetic field produced by an array of small coils. We discuss experimental results that illustrate the performance of MLDMs. A most interesting application of MLDMs comes from the fact they could be used to correct the aberrations of large and lower optical quality primary mirrors held by simple support systems. We estimate basic parameters of the needed MLDMs, obtaining reasonable values.

  6. Unlocking the potential of supported liquid phase catalysts with supercritical fluids: low temperature continuous flow catalysis with integrated product separation.

    PubMed

    Franciò, Giancarlo; Hintermair, Ulrich; Leitner, Walter

    2015-12-28

    Solution-phase catalysis using molecular transition metal complexes is an extremely powerful tool for chemical synthesis and a key technology for sustainable manufacturing. However, as the reaction complexity and thermal sensitivity of the catalytic system increase, engineering challenges associated with product separation and catalyst recovery can override the value of the product. This persistent downstream issue often renders industrial exploitation of homogeneous catalysis uneconomical despite impressive batch performance of the catalyst. In this regard, continuous-flow systems that allow steady-state homogeneous turnover in a stationary liquid phase while at the same time effecting integrated product separation at mild process temperatures represent a particularly attractive scenario. While continuous-flow processing is a standard procedure for large volume manufacturing, capitalizing on its potential in the realm of the molecular complexity of organic synthesis is still an emerging area that requires innovative solutions. Here we highlight some recent developments which have succeeded in realizing such systems by the combination of near- and supercritical fluids with homogeneous catalysts in supported liquid phases. The cases discussed exemplify how all three levels of continuous-flow homogeneous catalysis (catalyst system, separation strategy, process scheme) must be matched to locate viable process conditions. PMID:26574523

  7. Simultaneous Determination of Amitraz and its Metabolites in Blood by Support Liquid Extraction Using UPHLC-QTOF.

    PubMed

    Gao, Xue; Guo, Hao; Zhang, Wen-Wen; Gu, Chaokang

    2016-07-01

    This paper describes the use of UPHLC-QTOF for the analysis of pesticide amitraz and its metabolites in human blood. UPHLC-QTOF working in full scan mode simultaneously with a single MS/MS scan at 10 eV was employed to analyze in solid-support liquid-liquid extracts (SLE) of the human blood. Detection and quantification were carried out using full scan data (protonated molecules [M+H]+) while MS/MS data were used for fragment identification only. MS/MS scans were not found to have any negative influence on quantitation under the applied conditions. Verification studies were accomplished at low concentrations (1 ng/mL), and accuracy errors lower than 5 ppm were achieved. The human blood extracts spiked at LOQ and three QC fortification levels produced average recoveries in the range of 79.3-92.5% with relative standard deviations smaller than 10% for all analytes. Limits of detection (LODs) were between 0.1 and 0.5 ng/mL. Finally, the proposed method was successfully applied to a case of human poisoning. PMID:27339482

  8. Dynamic supported liquid membrane tip extraction of glyphosate and aminomethylphosphonic acid followed by capillary electrophoresis with contactless conductivity detection.

    PubMed

    See, Hong Heng; Hauser, Peter C; Sanagi, M Marsin; Ibrahim, Wan Aini Wan

    2010-09-10

    A dynamic supported liquid membrane tip extraction (SLMTE) procedure for the effective extraction and preconcentration of glyphosate (GLYP) and its metabolite aminomethylphosphonic acid (AMPA) in water has been investigated. The SLMTE procedure was performed in a semi-automated dynamic mode and demonstrated a greater performance against a static extraction. Several important extraction parameters such as donor phase pH, cationic carrier concentration, type of membrane solvent, type of acceptor stripping phase, agitation and extraction time were comprehensively optimized. A solution of Aliquat-336, a cationic carrier, in dihexyl ether was selected as the supported liquid incorporated into the membrane phase. Quantification of GLYP and AMPA was carried out using capillary electrophoresis with contactless conductivity detection. An electrolyte solution consisting of 12 mM histidine (His), 8 mM 2-(N-morpholino)ethanesulfonic acid (MES), 75 microM cetyltrimethylammonium bromide (CTAB), 3% methanol, pH 6.3, was used as running buffer. Under the optimum extraction conditions, the method showed good linearity in the range of 0.01-200 microg/L (GLYP) and 0.1-400 microg/L (AMPA), acceptable reproducibility (RSD 5-7%, n=5), low limits of detection of 0.005 microg/L for GLYP and 0.06 microg/L for AMPA, and satisfactory relative recoveries (90-94%). Due to the low cost, the SLMTE device was disposed after each run which additionally eliminated the possibility of carry-over between runs. The validated method was tested for the analysis of both analytes in spiked tap water and river water with good success. PMID:20696433

  9. Permeation of iridium(IV) and metal impurity chlorocomplexes through a supported liquid membrane designed for rhodium separation

    SciTech Connect

    Ashrafizadeh, S.N.; Demopoulos, G.P.; Rovira, M.; Sastre, A.M.

    1998-06-01

    A supported liquid membrane (SLM) system previously designed for Rh separation has been examined for its capability to reject the metal impurities which are commonly encountered in industrial Rh chloride solutions. Special attention was paid to Ir(IV) chlorocomplexes and their extraction/transport behavior against both conventional solvent extraction and supported liquid membrane systems of Kelex 100. A lab-scale SLM cell with an effective membrane area of 44 cm{sup 2} was used to conduct the SLM permeation tests. The SLM was composed of a Gore-Tex polymer substrate impregnated with an organic solution of Kelex 100, tridecanol, and kerosene. The impurities tested [in addition to Ir(IV)] were AG(I), As(V), Bi(III), Cd(II), Co(II), Cu(II), Fe(III), Ni(II), Pb(II), Pd(II), Pt(IV), Se(IV), Te(IV), and Zn(II). These impurities, based on their response against the SLM, were classified into three groups, i.e., those permeated through [Zn(II), Pb(II), Cd(II), Bi(III), Te(IV), and Ir(IV)], those nonpermeated at all [Ni(II), Co(II), As(V), Se(IV), Cu(II), and Fe(III)], and those blocking the membrane [Pt(IV), Pd(II), Ag(I), Pb(II), and Bi(III)]. The SLM was not capable of discriminating between Rh(III) and Ir(IV) transport at the optimum operating conditions. Complementary upstream and downstream processes are required to separate the impurities from the feed and the product solutions, respectively. Overall, this work revealed the great limitations of SLMs as effective and potentially useful separation media for the extraction of metals from industrial-like multicomponent aqueous feed solutions.

  10. Feasible way of Human Solid and Liquid Wastes' Inclusion Into Intersystem Mass Exchange of Biological-Technical Life Support Systems

    NASA Astrophysics Data System (ADS)

    Ushakova, Sofya; Tikhomirov, Alexander A.; Tikhomirova, Natalia; Kudenko, Yurii; Griboskaya, Illiada; Gros, Jean-Bernard; Lasseur, Christophe

    The basic objective arising at use of mineralized human solid and liquid wastes serving as the source of mineral elements for plants cultivation in biological-technical life support systems appears to be NaCl presence in them. The given work is aimed at feasibility study of mineralized human metabolites' utilization for nutrient solutions' preparation for their further employment at a long-term cultivation of uneven-aged wheat and Salicornia europaea L. cenosis in a conveyer regime. Human solid and liquid wastes were mineralized by the "wet incineration" method developed by Yu. Kudenko. On their base the solutions were prepared which were used for cultivation of 5-aged wheat conveyer with the time step-interval of 14 days. Wheat was cultivated by hydroponics method on expanded clay aggregate. For partial demineralization of nutrient solution every two weeks after regular wheat harvesting 12 L of solution was withdrawn from the wheat irrigation tank and used for Salicornia europaea cultivation by the water culture method in a conveyer regime. The Salicornia europaea conveyer was represented by 2 ages with the time step-interval of 14 days. Resulting from repeating withdrawal of the solution used for wheat cultivation, sodium concentration in the wheat irrigation solution did not exceed 400 mg/l, and mineral elements contained in the taken solution were used for Salicornia europaea cultivation. The experiment lasted 7 months. Total wheat biomass productivity averaged 30.1 g*m-2*day-1 at harvest index equal to 36.8The work was carried out under support of SB RAS grant 132 and INTAS 05-1000008-8010

  11. Evaluation of progesterone content in saliva using magnetic particle-based immuno supported liquid membrane assay (m-ISLMA).

    PubMed

    Tudorache, Madalina; Zdrojewska, Izabela Anna; Emnéus, Jenny

    2006-08-15

    Progesterone in saliva was monitored using a new method called magnetic particle-based immuno supported liquid membrane assay (m-ISLMA) in a sequential injection (SI) setup, allowing automatic sample cleanup, analyte enrichment, and detection in a single analysis unit. Progesterone (Ag) diffuses from a continuous flowing sample - the donor - into a supported organic liquid membrane (SLM), based on analyte partitioning (solubility) between the aqueous donor and the organic phase. The Ag is re-extracted from the SLM into a second stagnant aqueous acceptor, containing antibodies (Ab) immobilized on magnetic beads, held at the bottom of the acceptor by a magnet. Due to the formation of strong Ag-Ab-bead complexes and a large excess of Ab-beads, the Ag is accumulated and selectively enriched in the acceptor. The extracted progesterone was quantified by injecting into the acceptor a horseradish peroxidase (HRP) labeled analyte tracer, the substrate (luminol, H(2)O(2), and p-iodophenol), and finally detection of the generated chemiluminescence by a photomultiplier tube. After optimization of experimental parameters (e.g., sample flow rate, extraction time, type of organic solvent and antibody-bead concentration in the acceptor), a detection limit of 8.50+/-0.17 fgL(-1) and a dynamic range between 35 fgL(-1) and 10 pgL(-1) was reached. The progesterone level of saliva for three subjects (women in different period of ovarian cycle) was investigated, and the corresponding progesterone concentrations detected with m-ISLMA coincided well with the expected values. PMID:16473507

  12. Simultaneous determination of total fatty acid esters of chloropropanols in edible oils by gas chromatography-mass spectrometry with solid-supported liquid-liquid extraction.

    PubMed

    Liu, Qing; Han, Feng; Xie, Ke; Miao, Hong; Wu, Yongning

    2013-11-01

    This study aimed to establish a novel robust method for the simultaneous determination of total fatty acid esters of 4 chloropropanols including fatty acid esters of 3-monochloropropane-1,2-diol (3-MCPD esters), 2-monochloropropane-1,3-diol (2-MCPD esters), 1,3-dichloropropan-2-ol (1,3-DCP esters) and 2,3-dichloropropan-1-ol (2,3-DCP esters) in edible oils. In this method, sodium methylate in methanol was used as the reagent for the ester cleavage reaction of chloropropanols esters. The reaction products were extracted by a sodium sulfate solution, and then purified by solid-supported liquid-liquid extraction (SLE) using diatomaceous earth (Hydromatrix™) as the sorbent. Finally, the extracts were derivatized with heptafluorobutyrylim idazole (HFBI) and analyzed by gas chromatography-mass spectrometry (GC-MS). Quantification was achieved using deuterated chloropropanols as their respective internal standards, including 3-MCPD-d5, 2-MCPD-d5, 1,3-DCP-d5 and 2,3-DCP-d5. A good linear relationship between peak area and concentrations was obtained within the range of 0.025-2.000mgL(-1) with a correlation coefficients not less than 0.999 for all the chloropropanols esters. The limits of detection (LODs) of esters of 3-MCPD, 2-MCPD, 1,3-DCP and 2,3-DCP (calculated as corresponding chloropropanols) were 30, 30, 100 and 30μgkg(-1), respectively. The average recoveries of the 3-MCPD esters and the 4 chloropropanols spiked at 0.1, 0.5 and 2mgkg(-1) into blank oil matrix were typically in a range from 70.7% to 113.3%. The robust method validation data including calibration, LOD/LOQ, accuracy and repeatability and proficiency test results (Z-score: -0.5) of the official Food Analysis Performance Assessment Scheme (FAPAS) indicated that the present quantitative method could be successfully applied to the determination of total chloropropanols esters in various edible oils. PMID:24070627

  13. Separation and pre-concentration of glucocorticoids in water samples by ionic liquid supported vortex-assisted synergic microextraction and HPLC determination.

    PubMed

    Qin, Hui; Li, Bi; Liu, Mou Sheng; Yang, Ya Ling

    2013-04-01

    We have developed a synergic microextraction procedure based on ionic liquid for the pre-concentration and determination of glucocorticoids in water samples. Using nonionic surfactant Triton X-100 (TX-100) as synergic reagent, 1-butyl-3-methylimidazolium hexa-fluorophosphate accomplished extraction rapidly without heating in water bath. One key property of ionic liquids that highlights their potential is their wide liquid temperature range. The improved extraction was named as ionic liquid supported vortex-assisted synergic microextraction. Compared with the traditional liquid-liquid extraction and cloud point extraction, ionic liquid supported vortex-assisted synergic microextraction was accomplished in 8 min with considerably high recovery. The proposed method greatly improved the sensitivity of HPLC for the determination of glucocorticoids. The results obtained indicated a good linearity with the correlation coefficient of 0.997 over the range of 0.6-300 ng/mL and high sensitivity with LODs of 4.11, 9.19, and 7.50 ng/mL for hydrocortisone butyrate, beclomethasone dipropionate, and nandrolone phenylpropionate, respectively. The RSD of the method was 1.57-1.81% (n = 6) with enrichment factor of 99.85, and good recovery (≥97.24%). The method was successfully applied to the determination of glucocorticoids in mineral water, water of Dianchi lake, and tap water samples. PMID:23418157

  14. Use of halophytic plants for recycling NaCl in human liquid waste in a bioregenerative life support system

    NASA Astrophysics Data System (ADS)

    Balnokin, Yurii; Nikolai, Myasoedov; Larisa, Popova; Alexander, Tikhomirov; Sofya, Ushakova; Christophe, Lasseur; Jean-Bernard, Gros

    2010-09-01

    The purpose of this work was to develop technology for recycling NaCl containing in human liquid waste as intrasystem matter in a bioregenerative life support system (BLSS). The circulation of Na + and Cl - excreted in urine is achieved by inclusion of halophytes, i.e. plants that naturally inhabit salt-rich soils and accumulate NaCl in their organs. A model of Na + and Cl - recycling in a BLSS was designed, based on the NaCl turnover in the human-urine-nutrient solution-halophytic plant-human cycle. The study consisted of (i) selecting a halophyte suitable for inclusion in a BLSS, and (ii) determining growth conditions supporting maximal Na + and Cl - accumulation in the shoots of the halophyte growing in a nutrient solution simulating mineralized urine. For the selected halophytic plant, Salicornia europaea, growth rate under optimal conditions, biomass production and quantities of Na + and Cl - absorbed were determined. Characteristics of a plant production conveyor consisting of S.europaea at various ages, and allowing continuity of Na + and Cl - turnover, were estimated. It was shown that closure of the NaCl cycle in a BLSS can be attained if the daily ration of fresh Salicornia biomass for a BLSS inhabitant is approximately 360 g.

  15. Total Liquid Ventilation Provides Superior Respiratory Support to Conventional Mechanical Ventilation in a Large Animal Model of Severe Respiratory Failure

    PubMed Central

    Pohlmann, Joshua R; Brant, David O; Daul, Morgan A; Reoma, Junewai L; Kim, Anne C; Osterholzer, Kathryn R; Johnson, Kent J; Bartlett, Robert H; Cook, Keith E; Hirschl, Ronald B

    2011-01-01

    Total liquid ventilation (TLV) has the potential to provide respiratory support superior to conventional mechanical ventilation (CMV) in the acute respiratory distress syndrome (ARDS). However, laboratory studies are limited to trials in small animals for no longer than 4 hours. The objective of this study was to compare TLV and CMV in a large animal model of ARDS for 24 hours. Ten sheep weighing 53 ± 4 (SD) kg were anesthetized and ventilated with 100% oxygen. Oleic acid was injected into the pulmonary circulation until PaO2:FiO2 ≥ 60 mmHg, followed by transition to a protective CMV protocol (n=5) or TLV (n=5) for 24 hours. Pathophysiology was recorded and the lungs were harvested for histological analysis. Animals treated with CMV became progressively hypoxic and hypercarbic despite maximum ventilatory support. Sheep treated with TLV maintained normal blood gases with statistically greater PO2 (p<10−9) and lower PCO2 (p < 10−3) than the CMV group. Survival at 24 hours in the TLV and CMV groups were 100% and 40% respectively (p< 0.05). Thus, TLV provided gas exchange superior to CMV in this laboratory model of severe ARDS. PMID:21084968

  16. Controlled synthesis and electrocatalytic characteristics of Pt nanoparticles-supported nanographene synthesized by in-liquid plasma

    NASA Astrophysics Data System (ADS)

    Kondo, Hiroki; Amano, Tomoki; Ishikawa, Kenji; Sekine, Makoto; Hori, Masaru; Hiramatsu, Mineo; Meijo University Collaboration; Nagoya University Team

    2014-10-01

    We investigated a high-speed synthesis of high-crystallinity nanographenes over 1 micro-gram/min using in-liquid plasma. In this study, nanographene materials with different crystallinity were synthesized using ethanol and 1-butanol. Pt nanoparticles were supported on their surfaces reducing 8 wt%-H2PtCl6 in H2O. G-band and D-band peaks in Raman spectra indicated nanographene materials. Nanographene materials synthesized using ethanol have higher crystallinity than those synthesized using 1-butanol. According to X-ray diffraction patterns, sizes of Pt nanoparticles are almost similar regardless of alcohol types. In cyclic voltammetry characteristics, peaks related to adsorption and desorption of hydrogen were clearly found in the both cases. The platinum effective areas were estimated to be 208.5 and 147.63 m2/g for the cases using ethanol and 1-butanol, respectively. In addition, after potential cycling tests, nanographene materials synthesized using ethanol show almost no degradation, while those using 1-butanol show a drastic degradation. These results indicate that the higher-density Pt nanoparticles can be supported on the higher-crystallinity nanographene material and they show higher durability.

  17. Membrane supported liquid-liquid-liquid microextraction combined with field-amplified sample injection CE-UV for high-sensitivity analysis of six cardiovascular drugs in human urine sample.

    PubMed

    Zhou, Xiaoqing; He, Man; Chen, Beibei; Yang, Qing; Hu, Bin

    2016-05-01

    An effective dual preconcentration method involving off-line membrane supported liquid-liquid-liquid microextraction (MS-LLLME) and on-line field-amplified sample injection (FASI) was proposed for the extraction of six cardiovascular drugs, including mexiletine, xylocaine, propafenone, propranolol, metoprolol, and carvedilol from aqueous solution prior to CE-UV. In MS-LLLME, the analytes were extracted from 9 mL sample solution into toluene, and then back extracted into a drop of acceptor phase of 10 μL 20 mmol/L acetic acid. After that, the acceptor phase was directly introduced into CE for FASI without any modification. In FASI process, water plug was hydrodynamically injected (50 mbar, 3 s) into the capillary prior to sample injection (+6 kV, 18 s). Six target analytes were separated in less than 10 min at 25°C with a BGE consisting of 70 mmol/L Tris-H3 PO4 (pH 2.2) containing 10% v/v methanol. Under the optimized conditions, LODs obtained by the proposed MS-LLLME-FASI-CE-UV method were in the range of 0.02-0.82 μg/L (based on S/N = 3) with enrichment factors of 546- to 7300-fold for the target analytes. The RSDs of the developed method were in the range of 6.7-12.9% (n = 7). Good linearity (R(2) = 0.9928-0.9997) was obtained in concentration range of 0.1-100 μg/L for mexiletine and propranolol, 0.2-100 μg/L for xylocaine and metoprolol, 0.5-100 μg/L for propafenone and 2.0-100 μg/L for carvedilol, respectively. The developed method was successfully applied for real-time determination of metoprolol in human urine samples within 26 h after uptake. PMID:26763094

  18. Novel analytical procedure using a combination of hollow fiber supported liquid membrane and dispersive liquid-liquid microextraction for the determination of aflatoxins in soybean juice by high performance liquid chromatography - Fluorescence detector.

    PubMed

    Simão, Vanessa; Merib, Josias; Dias, Adriana N; Carasek, Eduardo

    2016-04-01

    This study describes a combination between hollow fiber membrane and dispersive liquid-liquid microextraction for determination of aflatoxins in soybean juice by HPLC. The main advantage of this approach is the use of non-chlorinated solvent and small amounts of organic solvents. The optimum extraction conditions were 1-octanol as immobilized solvent; toluene and acetone at 1:5 ratio as extraction and disperser solvents (100 μL), NaCl at 2% of the sample volume and extraction time of 60 min. The optimal condition for the liquid desorption was 150 μL acetonitrile:water (50:50 v/v) and desorption time of 20 min. The linear range varied from 0.03 to 21 μg L(-1), with R(2) coefficients ranging from 0.9940 to 0.9995. The limits of detection and quantification ranged from 0.01 μg L(-1) to 0.03 μg L(-1) and from 0.03 μg L(-1) to 0.1 μg L(-1), respectively. Recovery tests ranged from 72% to 117% and accuracy between 12% and 18%. PMID:26593494

  19. Ultrasensitive determination of cadmium in seawater by hollow fiber supported liquid membrane extraction coupled with graphite furnace atomic absorption spectrometry

    NASA Astrophysics Data System (ADS)

    Peng, Jin-feng; Liu, Rui; Liu, Jing-fu; He, Bin; Hu, Xia-lin; Jiang, Gui-bin

    2007-05-01

    A new procedure, based on hollow fiber supported liquid membrane preconcentration coupled with graphite furnace atomic absorption spectrometry (GFAAS) detection, was developed for the determination of trace Cd in seawater samples. With 1-octanol that contained a mixture of dithizone (carrier) and oleic acid immobilized in the pores of the polypropylene hollow fiber as a liquid membrane, Cd was selectively extracted from water samples into 0.05 M HNO 3 that filled the lumen of the hollow fiber as a stripping solution. The main extraction related parameters were optimized, and the effects of salinity and some coexisting interferants were also evaluated. Under the optimum extraction conditions, an enrichment factor of 387 was obtained for a 100-mL sample solution. In combination with graphite furnace atomic absorption spectrometry, a very low detection limit (0.8 ng L - 1 ) and a relative standard deviation (2.5% at 50 ng L - 1 level) were achieved. Five seawater samples were analyzed by the proposed method without dilution, with detected Cd concentration in the range of 56.4-264.8 ng L - 1 and the relative spiked recoveries over 89%. For comparison, these samples were also analyzed by the Inductively Coupled Plasma Mass Spectrometry (ICP-MS) method after a 10-fold dilution for matrix effect elimination. Statistical analysis with a one-way ANOVA shows no significant differences (at 0.05 level) between the results obtained by the proposed and ICP-MS methods. Additionally, analysis of certified reference materials (GBW (E) 080040) shows good agreement with the certified value. These results indicate that this present method is very sensitive and reliable, and can effectively eliminate complex matrix interferences in seawater samples.

  20. Electromembrane extraction of polar basic drugs from plasma with pure bis(2-ethylhexyl) phosphite as supported liquid membrane.

    PubMed

    Huang, Chuixiu; Seip, Knut Fredrik; Gjelstad, Astrid; Pedersen-Bjergaard, Stig

    2016-08-31

    Electromembrane extraction (EME) of polar basic drugs from human plasma was investigated for the first time using pure bis(2-ethylhexyl) phosphite (DEHPi) as the supported liquid membrane (SLM). The polar basic drugs metaraminol, benzamidine, sotalol, phenylpropanolamine, ephedrine, and trimethoprim were selected as model analytes, and were extracted from 300 μL of human plasma, through 10 μL of DEHPi as SLM, and into 100 μL of 10 mM formic acid as acceptor solution. The extraction potential across the SLM was 100 V, and extractions were performed for 20 min. After EME, the acceptor solutions were analyzed by high-performance liquid chromatography-ultraviolet detection (HPLC-UV). In contrast to other SLMs reported for polar basic drugs in the literature, the SLM of DEHPi was highly stable in contact with plasma, and the system-current across the SLM was easily kept below 50 μA. Thus, electrolysis in the sample and acceptor solution was kept at an acceptable level with no detrimental consequences. For the polar model analytes, representing a log P range from -0.40 to 1.32, recoveries in the range 25-91% were obtained from human plasma. Strong hydrogen bonding and dipole interactions were probably responsible for efficient transfer of the model analytes into the SLM, and this is the first report on efficient EME of highly polar analytes without using any ionic carrier in the SLM. PMID:27506347

  1. Determination of organochlorine pesticides in water using solvent cooling assisted dynamic hollow-fiber-supported headspace liquid-phase microextraction.

    PubMed

    Huang, Shih-Pin; Huang, Shang-Da

    2007-12-28

    The organic solvent film formed within a hollow fiber was used as an extraction interface in the headspace liquid-phase microextraction (HS-LPME) of organochlorine pesticides. Some common organic solvents with different vapor pressures (9.33-12,918.9 Pa) were studied as extractants. The results indicated that even the solvent with the highest vapor pressure (cyclohexane) can be used to carry out the extraction successfully. However, those compounds (analytes) with low vapor pressures could not be extracted successfully. In general, the large surface area of the hollow fiber can hasten the extraction speed, but it can increase the risk of solvent loss. Lowering the temperature of the extraction solvent could not only reduce solvent loss (by lowering its vapor pressure) but also extend the feasible extraction time to improve extraction efficiency. In this work, a solvent cooling assisted dynamic hollow-fiber-supported headspace liquid-phase microextraction (SC-DHF-HS-LPME) approach was developed. By lowering the temperature of the solvent, the evaporation can be decreased, the extraction time can be lengthened, and, on the contrary, the equilibrium constant between headspace phase and extraction solvent can be increased. In dynamic LPME, the extracting solvent is held within a hollow fiber, affixed to a syringe needle and placed in the headspace of the sample container. The extracting solvent within the fiber is moved to-and-fro by using a programmable syringe pump. The movement facilitates mass transfer of analyte(s) from the sample to the solvent. Analysis of the extract was carried out by gas chromatography-mass spectrometry (GC-MS). The effects of identity of extraction solvent, extraction temperature, sample agitation, extraction time, and salt concentration on extraction performance were also investigated. Good enrichments were achieved (65-211-fold) with this method. Good repeatabilities of extraction were obtained, with RSD values below 15.2%. Detection

  2. Supported Ionic Liquid Membranes and Ion-Jelly® Membranes with [BMIM][DCA]: Comparison of Its Performance for CO2 Separation

    PubMed Central

    Couto, Ricardo; Neves, Luísa; Simões, Pedro; Coelhoso, Isabel

    2015-01-01

    In this work, a supported ionic liquid membrane (SILM) was prepared by impregnating a PVDF membrane with 1-butyl-3-methylimidazolium dicyanamide ([BMIM][DCA]) ionic liquid. This membrane was tested for its permeability to pure gases (CO2, N2 and O2) and ideal selectivities were calculated. The SILM performance was also compared to that of Ion-Jelly® membranes, a new type of gelled membranes developed recently. It was found that the PVDF membrane presents permeabilities for pure gases similar or lower to those presented by the Ion-Jelly® membranes, but with increased ideal selectivities. This membrane presents also the highest ideal selectivity (73) for the separation of CO2 from N2 when compared with SILMs using the same PVDF support but with different ionic liquids. PMID:25594165

  3. Experimental investigation of the permeability and selectivity of supported ionic liquid membranes for CO2/He separation at temperatures up to 125° C

    SciTech Connect

    Ilconich, J.B.; Myers, C.R.; Pennline, H.W.; Luebke, D.R.

    2007-07-01

    Supported liquid membranes have been prepared by impregnation of commercial porous polymer films with the ionic liquid 1-n-hexyl-3- methylimidazolium bis(trifluoromethanesulfonyl)imide. The ionic liquid has been characterized, and the membranes have been tested to determine performance in the selective separation of CO2 from He. Experiments were conducted in a constant pressure system, and pure gas permeability/selectivity data are reported. Membranes prepared with polysulfone supports have been found to be stable to 125 °C. The CO2 permeability of the membranes increases from 744 to 1200 barrer as the temperature increases from 37 to 125 °C. The CO2/He selectivity decreased from 8.7 to 3.1 over the same temperature range.

  4. Highly cis-selective and lead-free hydrogenation of 2-hexyne by a supported Pd catalyst with an ionic-liquid layer.

    PubMed

    Schwab, Frederick; Weidler, Natascha; Lucas, Martin; Claus, Peter

    2014-09-18

    A simple Pd/SiO2 catalyst which was modified with the ionic liquid [BMPL][DCA] gave an excellent yield of 88% towards cis-2-hexene in the stereoselective hydrogenation of 2-hexyne. The catalyst outperforms, even at full conversion, the commonly used lead-poisoned, toxic Lindlar catalyst and supported colloidal-based Pd as well. PMID:25069061

  5. Supported phospholipid bilayer interaction with components found in typical room-temperature ionic liquids - a QCM-D and AFM study

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Quartz crystal microbalance with dissipation monitoring and atomic force microscopy were combined to evaluate the defects created by room-temperature ionic liquid anion and cation in a supported phospholipid bilayer composed of Zwitterionic lipids on a silica surface. The cation 1-octyl-3-methyl im...

  6. Determination of selected pharmaceutical compounds in biosolids by supported liquid extraction and gas chromatography-tandem mass spectrometry.

    PubMed

    Albero, Beatriz; Sánchez-Brunete, Consuelo; Miguel, Esther; Aznar, Ramón; Tadeo, José L

    2014-04-01

    In this work, an analytical method was developed for the determination of pharmaceutical drugs in biosolids. Samples were extracted with an acidic mixture of water and acetone (1:2, v/v) and supported liquid extraction was used for the clean-up of extracts, eluting with ethyl acetate:methanol (90:10, v/v). The compounds were determined by gas chromatography-tandem mass spectrometry using matrix-match calibration after silylation to form their t-butyldimethylsilyl derivatives. This method presents various advantages, such as a fairly simple operation for the analysis of complex matrices, the use of inexpensive glassware and low solvent volumes. Satisfactory mean recoveries were obtained with the developed method ranging from 70 to 120% with relative standard deviations (RSDs) ≤ 13%, and limits of detection between 0.5 and 3.6 ng g(-1). The method was then successfully applied to biosolids samples collected in Madrid and Catalonia (Spain). Eleven of the sixteen target compounds were detected in the studied samples, at levels up to 1.1 μg g(-1) (salicylic acid). Ibuprofen, caffeine, paracetamol and fenofibrate were detected in all of the samples analyzed. PMID:24582395

  7. Determination of free copper concentrations in natural waters by using supported liquid membrane extraction under equilibrium conditions.

    PubMed

    Romero, Roberto; Jönsson, Jan Ake

    2005-04-01

    A method is described for measurement of freely dissolved copper concentrations in natural water samples using supported liquid membrane (SLM) extraction under equilibrium conditions, a technique denoted "equilibrium sampling through membranes" (ESTM). For this purpose, 1,10-dibenzyl-1,10-diaza-18-crown-6 as neutral carrier and oleic acid were used in the membrane phase. The main variables optimised were the carrier used to form the metal complexes, the organic solvent used in the membrane, the countercation, pH, the ligand used in the acceptor phase, the extraction time, and the flow rate of the donor phase. After the optimisation process an enrichment factor of 18.5 was obtained. Equilibrium conditions were reached after extraction for 60 min if a flow rate of 1.0 mL min(-1) or greater was used. When different ligands such as humic acids, phthalic acid, and EDTA were added to the sample solution, and sample pH ranged from 6 to 8, the results obtained for freely dissolved copper concentrations were in a good agreement with results from speciation calculations performed with Visual Minteq V 2.30, Cheaqs V L20.1, and WinHumic V. The developed technique was applied to analysis of stream and leachate water. PMID:15759138

  8. Hydrogenation of Liquid Styrene by Alumina Supported Nickel Catalysts: Comparison between Classical and Non-Classical Methods

    NASA Astrophysics Data System (ADS)

    Tan, Y. C.; Abu Bakar, N. H. H.; Tan, W. L.; Abu Bakar, M.

    2016-06-01

    Almina supported Ni catalysts (Ni/Al2O3) with different Ni weight percentages (wt%) were prepared via classical and non-classical methods. All samples were prepared via impregnation technique. The samples prepared via non-classical methods were reduced using KBH4 as the reducing agent. The catalysts were tested for the hydrogenation of styrene in liquid phase. Optimum activation conditions for the hydrogenation reaction were found to be 633 K for 2 hours. Comparison of the catalytic reactivity for all catalysts at these activation conditions showed that catalysts prepared via classical methods exhibited better activity. Furthermore the 7.6wt% Ni-Al2O3/C showed enhanced activity when compared to the 5.9wt% and 13.8wt% Ni-Al2O3/C catalyst. This phenomenon is mainly attributed to the type of Ni active sites available on the catalyst. The surface properties of the catalysts investigated via H2- temperature programmed reduction (H2-TPR), H2-chemisorption and H2-temperature programmed desorption (H2-TPD) confirm this.

  9. Utilization of liquid human wastes and introduction into the material cycling in biological life-support systems

    NASA Astrophysics Data System (ADS)

    Kovaleva, N. P.>; Ushakova, S. A.; Gribovskaya, I. V.; Kudenko, U. A.

    The possibilities of step-by-step utilization of liquid human wastes in biological life-support systems on long-functioning space stations have been considered in this work. Utilization involves "wet" urine incineration with hydrogen peroxide at normal pressure and 90 - 95°C temperature, urease-enzymic decomposition of urine and biological desalination in the higher plant link. The soybean flour was used as a source of urease. Growing soya plants as a component of the higher plant link would give a steady source of urease to the system. To decompose urea (9-15g) contained in 1l of incinerated urine we used 0.5 - 1 g of soy flour. The duration of hydrolysis of daily urea excreted by a human is 70 - 95 hours. It is supposed that ammonia excreted in the reaction of urea decomposition will be processed by nitrifying bacteria. The concentration of total nitrogen in urine after urea hydrolysis and removal of ammonia formed during the reaction constituted 0.6 - 1.2 g/l. Further biological desalination was carried out in the higher plant link, for that the edible salt-accumulating halophytes Salicornia europaea were used. To grow this plant under the aqueous culture conditions, the urine was additionally mineralized at 180 °C after incineration and decomposition of urea. The process of additional mineralization was related to the necessity of removal of organic materials and nitrogen residues, which higher concentration under the aqueous culture conditions has negative effect on plants. The volume of the nutrient solution for growing 6 plants of Salicornia europaea was 1.5 l (daily norm of urine excreted by human), the planting area was 0.032 m2. By the end of vegetation the productivity and mineral composition of Salicornia europaea plants were analyzed. The productivity of plants grown on liquid human wastes (the experiment) practically was not different from the productivity of plants grown on the mineral solution with sodium chloride (checkout). In experimental

  10. Pumice-supported Pd-Pt bimetallic catalysts: Synthesis, structural characterization, and liquid-phase hydrogenation of 1,3-cyclooctadiene

    SciTech Connect

    Deganello, G.; Duca, D.; Liotta, L.F.; Martorana, A.; Venezia, M.; Benedetti, A.; Fagherazz, G.

    1995-01-01

    A series of pumice-supported palladium-platinum bimetallic catalysts were prepared and investigated by X-ray scattering (WAXS and SAXS) and XPS techniques. An alloy Pd-Pt was formed. The less abundant metal was found to segregate to the surface. The catalysts were tested in the liquid-phase hydrogenation of 1,3-cyclooctadiene to cyclooctene, and compared with similarly prepared pumice-supported palladium and platinum catalysts and other supported Pd-Pt catalysts reported in the literature. The addition of platinum reduces the activity and the selectivity of the palladium catalysts. Differences between the activity of these pumice-supported catalysts and the activity of previously described Pd and Pd-Pt catalysts on other supports, are attributed to the presence, in the latter, of diffusional processes. 50 refs., 4 figs. 2 tabs.

  11. Liquid phase methanol process development unit: installation, operation, and support studies, draft annual report. Technical progress report No. 8, October 1, 1982-September 30, 1983

    SciTech Connect

    Not Available

    1983-10-20

    Engineering of the 5 TPD LPMeOH PDU was completed, and significant progress was made at the LaPorte, TX site. The LaPorte installation work will be totally complete in mid-November 1983, and shakedown will begin as scheduled. Significant new data and results were achieved in the laboratory support programs at Fairfield and Allentown (APCI). Gas phase screening (0.5 inch tubular reactors) of new catalysts for liquid-entrained (slurry) operation was completed in Allentown. Investigation of some 25 new catalyst preparations led to the advancement of 3 catalyst candidates for liquid phase screening at Fairfield. The catalyst activity with both feed gases was stable, with long, slow deactivation observed (similar to Fairfield), an encouraging result. Laboratory progress at CSI, Fairfield was significant. Liquid phase screening of outside slurry catalyst candidates in the 2-liter stirred autoclave reactors was completed. Several outside catalyst powders achieved good performance in the liquid phase, and one commercial powder was recommended for advancement to LaPorte. In the fundamental modeling effort, the chemical equilibrium description for the methanol synthesis reaction was improved. Intrinsic kinetics were derived from the data from the stirred autoclave reactors. These kinetics were incorporated along with the gas holdup data into the three-phase backflow model of the liquid-entrained reactor. The model was subsequently used to make predictions of LaPorte performance, and to predict the data of the first Lab PDU slurry run. The early results are quite encouraging.

  12. Supported liquid membrane based removal of lead(II) and cadmium(II) from mixed feed: Conversion to solid waste by precipitation.

    PubMed

    Bhatluri, Kamal Kumar; Manna, Mriganka Sekhar; Ghoshal, Aloke Kumar; Saha, Prabirkumar

    2015-12-15

    Simultaneous removal of two heavy metals, lead(II) and cadmium(II), from mixed feed using supported liquid membrane (SLM) based technique is investigated in this work. The carrier-solvent combination of "sodium salt of Di-2-ethylhexylphosphoric acid (D2EHPA) (4% w/w) in environmentally benign coconut oil" was immobilized into the pores of solid polymeric polyvinylidene fluoride (PVDF) support. Sodium carbonate (Na2CO3) was used as the stripping agent. Carbonate salts of lead(II) and cadmium(II) were formed in the stripping side interface and they were insoluble in water leading to precipitation inside the stripping solution. The transportation of solute is positively affected due to the precipitation. Lead(II) removal was found to be preferential due to its favorable electronic configuration. The conversion of the liquid waste to the solid one was added advantage for the final removal of hazardous heavy metals. PMID:26252994

  13. Analysis of the organic liquid produced from catalytic cracking of crude palm oil in the presence of alumina supported catalysts

    NASA Astrophysics Data System (ADS)

    Ramli, Anita; Razak, Rozlina Abdul

    2012-09-01

    Catalytic cracking of crude palm oil (CPO) was studied in the presence of alumina, 1% Pt/Al2O3 and 1% Pd/Al2O3 as catalyst. The CPO to catalyst weight ratio used was 1:0.05. The experiment was carried out in a simple liquid-phase batch reactor at atmospheric pressure where the sample was heated to 300-350 δC. Products formed were organic liquid products (OLP) and gaseous product with the solid residue remains in the reactor. The total conversion of CPO was only between 25 - 31% where the residue is suggested to be mainly of polimerised CPO. The OLP was analysed using a gas chromatography with FID detector. Analyses show that the selectivity to liquid fuel is influence by the catalyst used whereby Al2O3 gives the highest selectivity to gasoline while 1% Pt/Al2O3 has the highest selectivity to diesel. However, 1% Pd/Al2O3 is not a suitable catalyst for catalytic cracking of CPO to liquid fuel where less than 17.5% of OLP produced could be classified as liquid fuel.

  14. Design, testing, fabrication and launch support of a liquid chemical barium release payload (utilizing the liquid fluorine-barium salt/hydrazine system)

    NASA Technical Reports Server (NTRS)

    Stokes, C. S.; Smith, E. W.; Murphy, W. J.

    1972-01-01

    A payload was designed which included a cryogenic oxidizer tank, a fuel tank, and burner section. Release of 30 lb of chemicals was planned to occur in 2 seconds at the optimum oxidizer to fuel ratio. The chemicals consisted of 17 lb of liquid fluorine oxidizer and 13 lb of hydrazine-barium salt fuel mixture. The fuel mixture was 17% barium chloride, 16% barium nitrate, and 67% hydrazine, and contained 2.6 lb of available barium. Two significant problem areas were resolved during the program: explosive valve development and burner operation. The release payload was flight tested, from Wallops Island, Virginia. The release took place at an altitude of approximately 260 km. The release produced a luminous cloud which expanded very rapidly, disappearing to the human eye in about 20 seconds. Barium ion concentration slowly increased over a wide area of sky until measurements were discontinued at sunrise (about 30 minutes).

  15. Rapid and simple pretreatment of human body fluids using electromembrane extraction across supported liquid membrane for capillary electrophoretic determination of lithium.

    PubMed

    Strieglerová, Lenka; Kubáň, Pavel; Boček, Petr

    2011-05-01

    Electromembrane extraction was used for simultaneous sample cleanup and preconcentration of lithium from untreated human body fluids. The sample of a body fluid was diluted 100 times with 0.5 mM Tris solution and lithium was extracted by electromigration through a supported liquid membrane composed of 1-octanol into 100 mM acetic acid acceptor solution. Matrix compounds, such as proteins, red blood cells, and other high-molecular-weight compounds were efficiently retained on the supported liquid membrane. The liquid membrane was anchored in pores of a short segment of a polypropylene hollow fiber, which represented a low cost, single use, disposable extraction unit and was discarded after each use. Acceptor solutions were analyzed using capillary electrophoresis with capacitively coupled contactless conductivity detection (CE-C(4) D) and baseline separation of lithium was achieved in a background electrolyte solution consisting of 18 mM L-histidine and 40 mM acetic acid at pH 4.6. Repeatability of the electromembrane extraction-CE-C(4) D method was evaluated for the determination of lithium in standard solutions and real samples and was better than 0.6 and 8.2% for migration times and peak areas, respectively. The concentration limit of detection of 9 nM was achieved. The developed method was applied to the determination of lithium in urine, blood serum, blood plasma, and whole blood at both endogenous and therapeutic concentration levels. PMID:21500213

  16. One-step synthesis of highly efficient nanocatalysts on the supports with hierarchical pores using porous ionic liquid-water gel.

    PubMed

    Kang, Xinchen; Zhang, Jianling; Shang, Wenting; Wu, Tianbin; Zhang, Peng; Han, Buxing; Wu, Zhonghua; Mo, Guang; Xing, Xueqing

    2014-03-12

    Stable porous ionic liquid-water gel induced by inorganic salts was created for the first time. The porous gel was used to develop a one-step method to synthesize supported metal nanocatalysts. Au/SiO2, Ru/SiO2, Pd/Cu(2-pymo)2 metal-organic framework (Cu-MOF), and Au/polyacrylamide (PAM) were synthesized, in which the supports had hierarchical meso- and macropores, the size of the metal nanocatalysts could be very small (<1 nm), and the size distribution was very narrow even when the metal loading amount was as high as 8 wt %. The catalysts were extremely active, selective, and stable for oxidative esterification of benzyl alcohol to methyl benzoate, benzene hydrogenation to cyclohexane, and oxidation of benzyl alcohol to benzaldehyde because they combined the advantages of the nanocatalysts of small size and hierarchical porosity of the supports. In addition, this method is very simple. PMID:24575937

  17. Data supporting the rat brain sample preparation and validation assays for simultaneous determination of 8 neurotransmitters and their metabolites using liquid chromatography-tandem mass spectrometry.

    PubMed

    Wojnicz, Aneta; Ortiz, José Avendaño; Casas, Ana I; Freitas, Andiara E; López, Manuela G; Ruiz-Nuño, Ana

    2016-06-01

    The data presented in this article supports the rat brain sample preparation procedure previous to its injection into the liquid chromatography-tandem mass spectrometry (LC-MS/MS) system to monitor levels of adrenaline, noradrenaline, glutamic acid, γ-aminobutyric acid, dopamine, 5-hydroxytryptamine, 5-hydroxyindole acetic acid, and 3-methoxy-4-hydroxyphenylglycol. In addition, we describe the method validation assays (such as calibration curve, lower limit of quantification, precision and accuracy intra- and inter-day, selectivity, extraction recovery and matrix effect, stability, and carry-over effect) according to the United States Food and Drug Administration and European Medicine Agency to measure in one step different neurotransmitters and their metabolites. The data supplied in this article is related to the research study entitled: "Simultaneous determination of 8 neurotransmitters and their metabolite levels in rat brain using liquid chromatography in tandem with mass spectrometry: application to the murine Nrf2 model of depression" (Wojnicz et al. 2016) [1]. PMID:27054183

  18. Novel supports in chiral stationary phase development for liquid chromatography. Preparation, characterization and application of ordered mesoporous silica particles.

    PubMed

    Sierra, Isabel; Pérez-Quintanilla, Damián; Morante, Sonia; Gañán, Judith

    2014-10-10

    Recent advances in the development of new materials are having a major impact on analytical chemistry. For example, the unique properties of ordered mesoporous silicas (OMSs) have been shown to enhance the analytical performance of many existing techniques or allow new, exciting ones to be developed. Likewise, the introduction of organo-functional groups makes OMSs highly versatile and enables them to perform specialized tasks, such as the separation of chiral compounds. This review provides an overview with the most relevant achievements in the preparation of OMS particles functionalized with chiral selectors. In addition, some examples from the last fifteen years regarding the analytical applications of functionalized OMS for chiral separations by high-performance liquid chromatography, ultra-high pressure high-performance liquid chromatography and capillary electrochromatography have been reviewed. PMID:25015243

  19. [Informational and analytical system for the support of decision making during liquidation of consequences of a large-scale radiation accident].

    PubMed

    Zlatoustov, N N; Bizin, I A; Bondarenko, I M; Kaganov, V M; Grenkova, G K

    2001-07-01

    The developed information and analytic system (IAS) of decision making support in liquidation medical-and-sanitary consequences of the large-scale radiation accidents permits on the base of computer models to evaluate the size and degree of territorial radioactive pollution, the radiation doses, the number and structure of radiation affection, the forces and means of medical service required for rendering the casualties the first medical aid as well as to compare the available and necessary medical forces and means. IAS is intended for equipping the toxicologist-radiologist's working place. To solve the private problems the IAS computer methods can be used both in complex and autonomously. PMID:11561428

  20. Partitioning of actinides from high level waste of PUREX origin using octylphenyl-N,N{prime}-diisobutylcarbamoylmethyl phosphine oxide (CMPO)-based supported liquid membrane

    SciTech Connect

    Ramanujam, A.; Dhami, P.S.; Gopalakrishnan, V.; Dudwadkar, N.L.; Chitnis, R.R.; Mathur, J.N.

    1999-06-01

    The present studies deal with the application of the supported liquid membrane (SLM) technique for partitioning of actinides from high level waste of PUREX origin. The process uses a solution of octylphenyl-N,N{prime}-diisobutylcarbamoylmethyl phosphine oxide (CMPO) in n-dodecane as a carrier with a polytetrafluoroethylene support and a mixture of citric acid, formic acid, and hydrazine hydrate as the receiving phase. The studies involve the investigation of such parameters as carrier concentration in SLM, acidity of the feed, and the feed composition. The studies indicated good transport of actinides like neptunium, americium, and plutonium across the membrane from nitric acid medium. A high concentration of uranium in the feed retards the transport of americium, suggesting the need for prior removal of uranium from the waste. The separation of actinides from uranium-lean simulated samples as well as actual high level waste has been found to be feasible using the above technique.

  1. Design and synthesis of redox-switched lariat ethers and their application for transport of alkali and alkaline-Earth metal cations across supported liquid membrane.

    PubMed

    Awasthy, Anubhuti; Bhatnagar, Mamta; Tomar, Jyoti; Sharma, Uma

    2006-01-01

    A new class of redox-switched anthraquinone derived lariat ethers 1-(1-anthraquinonyloxy) 3, 6, 9 trioxaundecane 11-ol (M(1)), 1-(1-anthraquinonyloxy) 3, 6 dioxaoctane 9-ol (M(2)), 1-(1-anthraquinonyloxy) 3 oxapentane 5-ol (M(3)), 1-(1-anthraquinonyloxy) 3 oxapentane 5-butane (M(4)), 1-(1-anthraquinonyloxy) 3, 6 dioxaoctane 9-methane (M(5)) and 1-(1-anthraquinonyloxy) 3 oxapentane 5-methane (M(6)) have been synthesized and characterized by spectral analysis. These ionophores were used in liquid membrane carrier facilitated transport of main group metal cations across supported liquid membrane (SLM). Cellulose nitrate membrane was used as membrane support. Effect of various parameters such as variation in concentration of metal as well as ionophore, effect of chain length and end group of ionophore have been studied. The sequence of metal ions transported by ionophore M(1) is Na(+) > Li(+) > K(+) > Ca(2+) > Mg(2+) and the order of metal ions transported by ionophores (M(2)-M(6)) is Li(+) > Na(+) > K(+) > Ca(2+) > Mg(2+). Ionophore M(1) is selective for Na(+), Li(+), and K(+) and ionophores (M(2)-M(6)) are selective for Li(+) and Na(+). PMID:17497021

  2. MEASUREMENTS TAKEN IN SUPPORT OF QUALIFICATION OF PROCESSING SAVANNAH RIVER SITE LOW-LEVEL LIQUID WASTE INTO SALTSTONE

    SciTech Connect

    Reigel, M.; Bibler, N.; Diprete, C.; Cozzi, A.; Staub, A.; Ray, J.

    2010-01-27

    The Saltstone Facility at the Savannah River Site (SRS) immobilizes low-level liquid waste into Saltstone to be disposed of in the Z-Area Saltstone Disposal Facility, Class Three Landfill. In order to meet the permit conditions and regulatory limits set by the South Carolina Department of Health and Environmental Control (SCDHEC), the Resource Conservation and Recovery Act (RCRA) and the Environmental Protection Agency (EPA), both the low-level salt solution and Saltstone samples are analyzed quarterly. Waste acceptance criteria (WAC) are designed to confirm the salt solution sample from the Tank Farm meets specific radioactive and chemical limits. The toxic characteristic leaching procedure (TCLP) is used to confirm that the treatment has immobilized the hazardous constituents of the salt solution. This paper discusses the methods used to characterize the salt solution and final Saltstone samples from 2007-2009.

  3. LIQUID PHASE SELECTIVE OXIDATION OF ETHYLBENZENE OVER ACTIVATED AL2O3 SUPPORTED V2O5 CATALYST

    EPA Science Inventory

    Acetophenone, a very useful industrial chemical for fragrance and flavoring agent and a solvent for plastics and resins, is usually produced as a byproduct of phenol production from cumeme. Aluminia supported vandium oxide catalyst is now explored for the selective oxidation of e...

  4. Density-fluctuation symbolic computation on the (3+1)-dimensional variable-coefficient Kudryashov-Sinelshchikov equation for a bubbly liquid with experimental support

    NASA Astrophysics Data System (ADS)

    Gao, Xin-Yi

    2016-06-01

    Liquids with gas bubbles are commonly seen in medical science, natural science, daily life and engineering. Nonlinear-wave symbolic computation on the (3+1)-dimensional variable-coefficient Kudryashov-Sinelshchikov model for a bubbly liquid is hereby performed. An auto-Bäcklund transformation and with some solitonic solutions are obtained. With respect to the density fluctuation of the bubble-liquid mixture, both the auto-Bäcklund transformation and solitonic solutions depend on the bubble-liquid-viscosity, transverse-perturbation, bubble-liquid-nonlinearity and bubble-liquid-dispersion coefficient functions. We note that some shock waves given by our solutions have been observed by the gas-bubble/liquid-mixture experiments. Effects on a bubbly liquid with respect to the bubble-liquid-viscosity, transverse-perturbation, bubble-liquid-nonlinearity and bubble-liquid-dispersion coefficient functions might be detected by the future gas-bubble/liquid-mixture experiments.

  5. Automation of static and dynamic non-dispersive liquid phase microextraction. Part 2: Approaches based on impregnated membranes and porous supports.

    PubMed

    Alexovič, Michal; Horstkotte, Burkhard; Solich, Petr; Sabo, Ján

    2016-02-11

    A critical overview on automation of modern liquid phase microextraction (LPME) approaches based on the liquid impregnation of porous sorbents and membranes is presented. It is the continuation of part 1, in which non-dispersive LPME techniques based on the use of the extraction phase (EP) in the form of drop, plug, film, or microflow have been surveyed. Compared to the approaches described in part 1, porous materials provide an improved support for the EP. Simultaneously they allow to enlarge its contact surface and to reduce the risk of loss by incident flow or by components of surrounding matrix. Solvent-impregnated membranes or hollow fibres are further ideally suited for analyte extraction with simultaneous or subsequent back-extraction. Their use can therefore improve the procedure robustness and reproducibility as well as it "opens the door" to the new operation modes and fields of application. However, additional work and time are required for membrane replacement and renewed impregnation. Automation of porous support-based and membrane-based approaches plays an important role in the achievement of better reliability, rapidness, and reproducibility compared to manual assays. Automated renewal of the extraction solvent and coupling of sample pretreatment with the detection instrumentation can be named as examples. The different LPME methodologies using impregnated membranes and porous supports for the extraction phase and the different strategies of their automation, and their analytical applications are comprehensively described and discussed in this part. Finally, an outlook on future demands and perspectives of LPME techniques from both parts as a promising area in the field of sample pretreatment is given. PMID:26802999

  6. Hollow-fiber-supported liquid-phase microextraction using an ionic liquid as the extractant for the pre-concentration of bisphenol A, 17-β-estradiol, estrone and diethylstilbestrol from water samples with HPLC detection.

    PubMed

    Zou, Yanmin; Zhang, Zhen; Shao, Xiaoling; Chen, Yao; Wu, Xiangyang; Yang, Liuqing; Zhu, Jingjing; Zhang, Dongmei

    2014-01-01

    A new method for the determination of four endocrine disrupting compounds (EDCs) (bisphenol A, 17-β-estradiol, estrone and diethylstilbestrol) in water samples has been developed using polypropylene hollow-fiber-supported ionic liquid (IL, 1-Octyl-3-methylimidazolium hexafluorophosphate, [C8MIM][PF6]) microextraction [HF-liquid-phase microextraction (LPME)] combined with high-performance liquid chromatography (HPLC)/UV. This method was used to investigate pollutants in surface water, on the Neijiang River, located at Zhenjiang, Jiangsu Province. Several parameters (sample pH, volume of accepter phase, ionic strength) were investigated. Under the optimum extraction conditions (sample pH, 2.0; volume of extraction solvent, 2.5 μL; ionic strength, 2.57) the proposed method offered: good linearity range, 0.15-100 μg L(-1), with the correlation coefficients (r(2)) of 0.9996, 0.9994, 0.9990 and 0.9984, respectively; low limits of detection, 0.03, 0.05, 0.10, 0.05 μg L(-1) (S/N = 3) for bisphenol A, 17-β-estradiol, estrone and diethylstilbestrol, respectively; good reproducibility (relative standard deviation (RSD), 8.41, 7.61, 9.00, 7.22%, respectively, n = 5); satisfactory recoveries (80.2-107.1%, n = 5); and high enrichment factors, 5,240, 3,693, 2,425 and 2,086, were achieved, for the four chemicals, respectively. Using the proposed HF-LPME, among 15 sampling sites along Neijiang River, bisphenol A, diethylstilbestrol and 17-β-estradiol were detected in some sites, all of which were the near suburban sampling sites. The results indicate that the role of municipal sewage is an important source of EDC contamination. PMID:24622552

  7. Liquid-Phase Synthesis of 2′-Methyl-RNA on a Homostar Support through Organic-Solvent Nanofiltration

    PubMed Central

    Gaffney, Piers R J; Kim, Jeong F; Valtcheva, Irina B; Williams, Glynn D; Anson, Mike S; Buswell, Andrew M; Livingston, Andrew G

    2015-01-01

    Due to the discovery of RNAi, oligonucleotides (oligos) have re-emerged as a major pharmaceutical target that may soon be required in ton quantities. However, it is questionable whether solid-phase oligo synthesis (SPOS) methods can provide a scalable synthesis. Liquid-phase oligo synthesis (LPOS) is intrinsically scalable and amenable to standard industrial batch synthesis techniques. However, most reported LPOS strategies rely upon at least one precipitation per chain extension cycle to separate the growing oligonucleotide from reaction debris. Precipitation can be difficult to develop and control on an industrial scale and, because many precipitations would be required to prepare a therapeutic oligonucleotide, we contend that this approach is not viable for large-scale industrial preparation. We are developing an LPOS synthetic strategy for 2′-methyl RNA phosphorothioate that is more amenable to standard batch production techniques, using organic solvent nanofiltration (OSN) as the critical scalable separation technology. We report the first LPOS-OSN preparation of a 2′-Me RNA phosphorothioate 9-mer, using commercial phosphoramidite monomers, and monitoring all reactions by HPLC, 31P NMR spectroscopy and MS. PMID:26012874

  8. Functionalized mesoporous silica supported copper(II) and nickel(II) catalysts for liquid phase oxidation of olefins.

    PubMed

    Nandi, Mahasweta; Roy, Partha; Uyama, Hiroshi; Bhaumik, Asim

    2011-12-14

    Highly ordered 2D-hexagonal mesoporous silica has been functionalized with 3-aminopropyltriethoxysilane (3-APTES). This is followed by its condensation with a dialdehyde, 4-methyl-2,6-diformylphenol to produce an immobilized Schiff-base ligand (I). This material is separately treated with methanolic solution of copper(II) chloride and nickel(II) chloride to obtain copper and nickel anchored mesoporous materials, designated as Cu-AMM and Ni-AMM, respectively. The materials have been characterized by Fourier transform infrared (FT-IR) and UV-vis diffuse reflectance (DRS) spectroscopy, powder X-ray diffraction (XRD), transmission electron microscopy (TEM), N(2) adsorption-desorption studies and (13)C CP MAS NMR spectroscopy. The metal-grafted mesoporous materials have been used as catalysts for the efficient and selective epoxidation of alkenes, viz. cyclohexene, trans-stilbene, styrene, α-methyl styrene, cyclooctene and norbornene to their corresponding epoxides in the presence of tert-butyl hydroperoxide (TBHP) as the oxidant under mild liquid phase conditions. PMID:21989952

  9. Passive extraction and clean-up of phenoxy acid herbicides in samples from a groundwater plume using hollow fiber supported liquid membranes.

    PubMed

    Liu, Jing-Fu; Toräng, Lars; Mayer, Philipp; Jönsson, Jan Ake

    2007-08-10

    Hollow fiber supported liquid membranes were applied for the passive extraction of phenoxy acid herbicides from water samples. Polypropylene hollow fiber membranes (240 microm i.d., 30 microm wall thickness, 0.05 microm pore size, 30 cm length) were impregnated with 2.0% tri-n-octylphosphine oxide (TOPO) in di-n-hexyl ether in the pores of the fiber wall to form a liquid membrane. They were then filled with basic solution in the lumen as acceptor and finally placed into the sample (donor). Complete extraction of phenoxy acid herbicides including 2,4-D, MCPA, dichlorprop, and mecoprop from an acidified sample (4 mL, adjusted to pH 1.5 with HCl) into basic acceptor (10 microL of 0.2M NaOH) was achieved after 4 h of shaking (100 rpm) resulting in an enrichment factor of 400 times. The acceptor was then neutralized by addition of HCl and injected into a HPLC system for the determination of the phenoxy acid herbicides. Environmentally relevant salinity (0-3.5% NaCl) and dissolved organic matter (0-25 mg/L of dissolved organic carbon) had no significant effect on the extraction. The method provided extraction efficiencies of more than 91%, detection limits of 0.3-0.6 microg/L, and combined extraction and clean up in one single step. This procedure was applied to determine aqueous concentrations of phenoxy acid herbicides in groundwater samples collected from an old dumping site (Cheminova, Denmark) with detected concentrations up to 5800 microg/L. Although the samples were very dirty with large amounts of suspended particles, non-aqueous phase liquids (NAPLs) and dissolved organic matters, good spike recoveries (80-126%) were obtained for 10 of the 11 samples. PMID:17449052

  10. Derivatization of ethylene dibromide with silica-supported silver picrate for improved high-performance liquid chromatographic detection

    SciTech Connect

    Colgan, S.T.; Krull, I.S.; Dorschel, C.; Bidlingmeyer, B.

    1986-10-01

    Silica-supported silver picrate was used as an off-line, precolumn derivatization reagent for ethylene dibromide (EDB). Two products were obtained, the ratio of which, as a function of reaction conditions, is characteristic of EDB. The derivatives were monitored with UV, reductive electrochemical, and photolysis/oxidative electrochemical detection. Sub-parts-per-billion detection limits were obtained. The method was used to quantitate EDB in leaded gasoline, and the results were confirmed with gas chromatography with electron capture detection (GC/ECD). The method was further validated with a single blind analysis of spiked EDB in gasoline. This is the first report of an HPLC method for EDB.

  11. Core-Shell Diamond as a Support for Solid-Phase Extraction and High-Performance Liquid Chromatography

    SciTech Connect

    Saini, Gaurav; Jensen, David S.; Wiest, Landon A.; Vail, Michael A.; Dadson, Andrew; Lee, Milton L.; Shutthanandan, V.; Linford, Matthew R.

    2010-06-01

    We report the formation of core-shell diamond particles for solid phase extraction (SPE) and high performance liquid chromatography (HPLC) made by layer-by-layer (LbL) deposition. Their synthesis begins with the amine functionalization of microdiamond by its immersion in an aqueous solution of a primary amine-containing polymer (polyallylamine (PAAm)). The amine-terminated microdiamond is then immersed in an aqueous suspension of nanodiamond, which leads to adsorption of the nanodiamond. Alternating (self-limiting) immersions in the solutions of the amine-containing polymer and the suspension of nanodiamond are continued until the desired number of nanodiamond layers is formed around the microdiamond. Finally, the core-shell particles are cross-linked with 1,2,5,6-diepoxycyclooctane or reacted with 1,2-epoxyoctadecane. Layer-by-layer deposition of PAAm and nanodiamond is also studied on planar Si/SiO2 surfaces, which were characterized by SEM, Rutherford backscattering spectrometry (RBS) and nuclear reaction analysis (NRA). Core-shell particles are characterized by diffuse reflectance infrared Fourier transform spectroscopy (DRIFT), environmental scanning electron microscopy (ESEM), and Brunauer Emmett Teller (BET) surface area and pore size measurements. Larger (ca. 50 μm) core-shell diamond particles have much higher surface areas, and analyte loading capacities in SPE than nonporous solid diamond particles. Smaller (ca. 3 μm), normal and reversed phase, core-shell diamond particles have been used for HPLC, with 36,300 plates per meter for mesitylene in a separation of benzene and alkyl benzenes on a C18 adsorbent, and 54,800 plates per meter for diazinon in a similar separation of two pesticides.

  12. Separation of gallium and arsenic in wafer grinding extraction solution using a supported liquid membrane that contains PC88A as a carrier.

    PubMed

    Tsai, Chin-Ying; Chen, Yi-Fu; Chen, Wen-Ching; Yang, Fong-Ru; Chen, Jyh-Herng; Lin, Jing-Chie

    2005-01-01

    Wafer grinding extraction solution was passed through a supported liquid membrane (SLM) that contained PC88A (2-ethylhexyl phosphonic acid mono 2-ethylhexyl ester) as a carrier, to separate gallium from arsenic by selective permeation. The SLM separation process was conducted under various conditions. The kind of membrane supporter, the pH of the feed, the feed concentration, and the HCl content in the strip governed the concentration of gallium and arsenic in the strip phase. The conditions determined as optimal in the laboratory test were used to perform the pilot test. Well separation between gallium and arsenic was performed in both laboratory and pilot tests. Hydrophobic membrane polytetrafluoroethylene (PTFE) with 0.2 microm pores was the best of three membrane supporters. The most efficient separation was obtained using an acidic feed (pH at 1.8) with 1000 ppm gallium. Over a 12-h period of stripping, the striped Ga concentration increased with the HCl concentration from 0.5 to 2.0 M and then leveled off. The recovery rate in the pilot test exceeded that on the laboratory scale because the membrane area was greater. The pilot test yielded a high recovery percentage of gallium (at 91%) and a low recovery of arsenic (merely 1.3 ppm) in the strip over 72 h. PMID:15717789

  13. Data supporting the rat brain sample preparation and validation assays for simultaneous determination of 8 neurotransmitters and their metabolites using liquid chromatography–tandem mass spectrometry

    PubMed Central

    Wojnicz, Aneta; Ortiz, José Avendaño; Casas, Ana I.; Freitas, Andiara E.; López, Manuela G.; Ruiz-Nuño, Ana

    2016-01-01

    The data presented in this article supports the rat brain sample preparation procedure previous to its injection into the liquid chromatography–tandem mass spectrometry (LC–MS/MS) system to monitor levels of adrenaline, noradrenaline, glutamic acid, γ-aminobutyric acid, dopamine, 5-hydroxytryptamine, 5-hydroxyindole acetic acid, and 3-methoxy-4-hydroxyphenylglycol. In addition, we describe the method validation assays (such as calibration curve, lower limit of quantification, precision and accuracy intra- and inter-day, selectivity, extraction recovery and matrix effect, stability, and carry-over effect) according to the United States Food and Drug Administration and European Medicine Agency to measure in one step different neurotransmitters and their metabolites. The data supplied in this article is related to the research study entitled: “Simultaneous determination of 8 neurotransmitters and their metabolite levels in rat brain using liquid chromatography in tandem with mass spectrometry: application to the murine Nrf2 model of depression” (Wojnicz et al. 2016) [1]. PMID:27054183

  14. Cr(VI) transport via a supported ionic liquid membrane containing CYPHOS IL101 as carrier: system analysis and optimization through experimental design strategies.

    PubMed

    Rodríguez de San Miguel, Eduardo; Vital, Xóchitl; de Gyves, Josefina

    2014-05-30

    Chromium(VI) transport through a supported liquid membrane (SLM) system containing the commercial ionic liquid CYPHOS IL101 as carrier was studied. A reducing stripping phase was used as a mean to increase recovery and to simultaneously transform Cr(VI) into a less toxic residue for disposal or reuse. General functions which describe the time-depending evolution of the metal fractions in the cell compartments were defined and used in data evaluation. An experimental design strategy, using factorial and central-composite design matrices, was applied to assess the influence of the extractant, NaOH and citrate concentrations in the different phases, while a desirability function scheme allowed the synchronized optimization of depletion and recovery of the analyte. The mechanism for chromium permeation was analyzed and discussed to contribute to the understanding of the transfer process. The influence of metal concentration was evaluated as well. The presence of different interfering ions (Ca(2+), Al(3+), NO3(-), SO4(2-), and Cl(-)) at several Cr(VI): interfering ion ratios was studied through the use of a Plackett and Burman experimental design matrix. Under optimized conditions 90% of recovery was obtained from a feed solution containing 7mgL(-1) of Cr(VI) in 0.01moldm(-3) HCl medium after 5h of pertraction. PMID:24751491

  15. Miniaturized supported liquid membrane device for selective on-line enrichment of basic drugs in plasma combined with capillary zone electrophoresis.

    PubMed

    Pálmarsdóttir, S; Thordarson, E; Edholm, L E; Jönsson, J A; Mathiasson, L

    1997-05-01

    A hollow fiber miniaturized supported liquid membrane (SLM) device for sample preparation is connected on-line with capillary electrophoresis and used for determination of a basic drug, bambuterol, in human plasma. The analyte is extracted from the outside of the hollow fiber (donor) through the liquid membrane (pores of the fiber impregnated with organic solvent) into the acceptor solution in the fiber lumen. The process is driven by differences in pH between the donor and acceptor solution. The whole volume of the acceptor solution can then be injected into the CZE capillary by using the double-stacking procedure for large volume-injection. Very clean extracts of low ionic strength are obtained from the SLM treatment, making this sample pretreatment method compatible with the CZE double-stacking procedure, which in turn makes it possible to inject large volumes of sample onto the separation capillary. Good performance of the whole procedure is demonstrated, and detection limits in the low nanomolar range were obtained in spite of the relatively weak UV absorbance of bambuterol. Extractions through the miniaturized SLM unit can be performed for 5-6 h without regenerating the fiber. The regeneration procedure was tested, and no relevant changes in the performance of the extraction could be found after seven regenerations, allowing the same fiber to be used for a week. PMID:9145027

  16. Hollow-fibre supported liquid membrane extraction for determination of fluoxetine and norfluoxetine concentration at ultra trace level in sewage samples.

    PubMed

    Zorita, Saioa; Mårtensson, Lennart; Mathiasson, Lennart

    2007-10-01

    In this study, a method was developed for determining the concentration of the pharmaceutical fluoxetine and its metabolite, norfluoxetine, in sewage water samples. Sample preparation was performed by hollow-fibre supported liquid membrane (HF-SLM) extraction with final analysis using liquid chromatography with UV detection. Several parameters were studied including type of organic solvent, sample and acceptor pH, and salt and humic acid content. The optimised method allowed determination of the analyte at the ng/L level in sewage water. A linear plot gave a correlation coefficient better than 0.991 for both analytes and resulted in limits of detection in sewage water of 11 and 12 ng/L, for fluoxetine and norfluoxetine, respectively. The enrichment factor was over 1700 for both analytes in sewage water. The repeatability and reproducibility were better than 8% and 17%, respectively. The developed methodology was used to study daily variations of fluoxetine and norfluoxetine in municipal sewage streams. Norfluoxetine has been detected for the first time in sewage water and a preliminary analysis gave average concentrations of 150 and 225 ng/L for norfluoxetine and fluoxetine, respectively. PMID:17763523

  17. Permeation of mixtures of four phenols through a supported liquid membrane in NaCl 1.0 mol/dm{sup 3} medium

    SciTech Connect

    Arana, G.; Borge, G.; Etxebarria, N.; Fernandez, L.A.

    1999-02-01

    The permeation of four phenols (phenol, 2-chlorophenol, 2-nitrophenol, and 2,4-dichlorophenol) through a supported liquid membrane has been studied in NaCl 1.0 mol/dm{sup 3} medium. The flux of each phenol was determined by measuring in real time the change of their concentration in the strip phase by making use of a fiber optic spectrophotometer and a multivariate calibration. The model for the permeation of phenol alone was first developed by making permeation experiments of a phenol, and then permeation studies of the mixture were carried out and the model was extended to those phenols. It was found that the permeation of a phenol is interfered with by the presence of other phenols.

  18. Automatic Supported Liquid Extraction (SLE) Coupled with HILIC-MS/MS: An Application to Method Development and Validation of Erlotinib in Human Plasma

    PubMed Central

    Pan, Jiongwei; Jiang, Xiangyu; Chen, Yu-Luan

    2010-01-01

    A novel bioanalytical method was developed and validated for the quantitative determination of erlotinib in human plasma by using the supported liquid extraction (SLE) sample cleanup coupled with hydrophilic interaction liquid chromatography and tandem mass spectrometric detection (HILIC-MS/MS). The SLE extract could be directly injected into the HILIC-MS/MS system for analysis without the solvent evaporation and reconstitution steps. Therefore, the method is simple and rapid. In the present method, erlotinib-d6 was used as the internal standard. The SLE extraction recovery was 101.3%. The validated linear curve range was 2 to 2,000 ng/mL based on a sample volume of 0.100-mL, with a linear correlation coefficient of > 0.999. The validation results demonstrated that the present method gave a satisfactory precision and accuracy: intra-day CV < 5.9% (<8.4% for the lower limit of quantitation, LLOQ) with n = 6 and the accuracy of 98.0–106.0%; inter-day CV < 3.2% (<1.5% for LLOQ) with n = 18 and the accuracy of 100.0–103.2%. A dilution factor of 10 with blank plasma was validated for partial volume analysis. The stability tests indicated that the erlotinib in human plasma is stable for three freeze-thaw cycles (100.0–104.5% of the nominal values), or 24-h ambient storage (100.0–104.8% of the nominal values), or 227-day frozen storage at both -20 °C (91.5–94.5% of the nominal values) and -70 °C (93.3–93.8% of the nominal values). The results also showed no significant matrix effect (<6.3%) even with direct injection of organic extract into the LC-MS/MS system. The validated method has been successfully applied to support a clinical study.

  19. Polymer-supported ionic liquid solid phase extraction for trace inorganic and organic mercury determination in water samples by flow injection-cold vapor atomic absorption spectrometry.

    PubMed

    Escudero, Leticia B; Olsina, Roberto A; Wuilloud, Rodolfo G

    2013-11-15

    A simple and green technique named polymer-supported ionic liquid solid phase extraction (PSIL-SPE) was developed for mercury (Hg) species determination. Inorganic Hg (InHg) species was complexed with chloride ions followed by its introduction into a flow injection on-line system to quantitatively retain the anionic chlorocomplex (HgCl4(2-)) in a column packed with CYPHOS(®) IL 101-impregnated resin. The trapped InHg was then reduced with stannous chloride (SnCl2) and eluted with the same flow of reducing agent followed by cold vapor atomic absorption spectrometry (CV-AAS) detection. Organic mercury species (OrgHg) did not interact with the impregnated resin and were not retained into the column. Total concentration of OrgHg was evaluated by difference between total Hg and InHg concentration. A 95% extraction efficiency was achieved for InHg when the procedure was developed under optimal experimental conditions. The limit of detection obtained for preconcentration of 40 mL of sample was 2.4 ng L(-1) InHg. The relative standard deviation (RSD) was 2.7% (at 1 µg L(-1) InHg and n=10) calculated from the peak height of absorbance signals (Gaussian-shape and reproducible peaks). This work reports the first polymer-supported IL solid phase extraction approach implemented in a flow injection on-line system for determination of Hg species in mineral, tap and river water samples. PMID:24148384

  20. The impact of recent innovations in the use of liquid chromatography-mass spectrometry in support of drug metabolism studies: are we all the way there yet?

    PubMed

    Nassar, Alaa-Eldin F; Talaat, Rasmy E; Kamel, Amin M

    2006-01-01

    Absorption, distribution, metabolism, excretion and toxicology (ADMET) studies are widely used in drug discovery and development to help obtain the optimal balance of properties necessary to convert lead compounds into drugs that are safe and effective for human use. Drug discovery efforts have been aimed at identifying and addressing metabolism issues at the earliest possible stage, by developing and applying innovative liquid chromatography-mass spectrometry (LC-MS)-based techniques and instrumentation, which are both faster and more accurate than prior techniques. Such new approaches are demonstrating considerable potential to improve the overall safety profile of drug candidates throughout the drug discovery and development process. These emerging techniques streamline and accelerate the process by eliminating potentially harmful candidates earlier and improving the safety of new drugs. In the area of drug metabolism, for example, revolutionary changes have been achieved by the combination of LC-MS with innovative instrumentation such as triple quadrupoles, ion traps and time-of-flight mass spectrometry. In turn, most ADMET studies have come to rely on LC-MS for the analysis of an ever-increasing workload of potential candidates. This article provides a discussion on the importance of LC-MS in supporting drug metabolism studies, and highlights the relative merits of current applications for LC-MS in drug metabolism testing and analysis. These applications include in vitro and in vivo testing, pharmacokinetic profiling, chiral separations, stable isotope labeling, metabolic activation testing, metabolite characterization and radiolabeled-drug testing. PMID:16445118

  1. Cadmium accumulation by a Citrobacter sp. immobilized on gel and solid supports: applicability to the treatment of liquid wastes containing heavy metal cations

    SciTech Connect

    Macaskie, L.E.; Wates, J.M.; Dean, A.C.R.

    1987-01-01

    Polyacrylamide gel-immobilized cells of a Citrobacter sp. removed cadmium from flows supplemented with glycerol 2-phosphate, the metal uptake mechanism being mediated by the activity of a cell-bound phosphatase that precipitates liberated inorganic phosphate with heavy metals at the cell surface. The constraints of elevated flow rate and temperature were investigated and the results discussed in terms of the kinetics of immobilized enzymes. Loss in activity with respect to cadmium accumulation but not inorganic phosphate liberation was observed at acid pH and was attributed to the pH-dependent solubility of cadmium phosphate. Similarly high concentrations of chloride ions, and traces of cyanide inhibited cadmium uptake and this was attributed to the ability of these anions to complex heavy metals, especially the ability of CN/sup -/ to form complex anions with Cd/sup 2 +/. The data are discussed in terms of the known chemistry of chloride and cyanide-cadmium complexes and the relevance of these factors in the treatment of metal-containing liquid wastes is discussed. The cells immobilized in polyacrylamide provided a convenient small-scale laboratory model system. It was found that the Citrobacter sp. could be immobilized on glass supports with no chemical treatment or modification necessary. Such cells were also effective in metal accumulation and a prototype system more applicable to the treatment of metal-containing streams on a larger scale is described.

  2. An ultrasensitive lysozyme chemiluminescence biosensor based on surface molecular imprinting using ionic liquid modified magnetic graphene oxide/β-cyclodextrin as supporting material.

    PubMed

    Duan, Huimin; Wang, Xiaojiao; Wang, Yanhui; Sun, Yuanling; Li, Jianbo; Luo, Chuannan

    2016-04-28

    In this work, ionic liquid modified Fe3O4@dopamine/graphene oxide/β-cyclodextrin (ILs-Fe3O4@DA/GO/β-CD) was used as supporting material to synthesize surface molecularly imprinted polymer (SMIP) which then was introduced into chemiluminescence (CL) to achieve an ultrasensitive and selective biosensor for determination of lysozyme (Lys). ILs and β-CD was applied to provide multiple binding sites to prepare Lys SMIP and Fe3O4@DA was designed to make the product separate easily and prevent the aggregation of GO which could improve absorption capacity for its large specific surface area. The ILs-Fe3O4@DA/GO/β-CD-SMIP showed high adsorption capacity (Q = 101 mg/g) to Lys in the adsorption isotherm assays. The adsorption equilibrium was reached within 10 min for all the concentrations, attributing to the binding sites situated exclusively at the surface, and the adsorption model followed Langmuir isotherm. Under the suitable CL conditions, the proposed biosensor could response Lys linearly in the range of 1.0 × 10(-9)-8.0 × 10(-8) mg/mL with a detection limit of 3.0 × 10(-10) mg/mL. When used in practical samples in determination of Lys, the efficient biosensor exhibited excellent result with the recoveries ranging from 94% to 112%. PMID:27046214

  3. Selective transport of copper(I, II), cadmium(II), and zinc(II) ions through a supported liquid membrane containing bathocuproine, neocuproine, or bathophenanthroline

    SciTech Connect

    Saito, Takashi )

    1994-06-01

    Some selective transport systems for heavy metallic ions through a supported liquid membrane (SLM) containing a 2,2[prime]-dipyridyl derivative ligand, 4,7-diphenyl-2,9-dimethyl-1, 10-phenanthroline (bathocuproine), 2,9-dimethyl-1,10-phenanthroline (neocuproine), or 4,7-diphenyl-1,10-phenanthroline (bathophenanthroline), were investigated. The transport of copper(I, II), cadmium(II), zinc(II), lead(II), and cobalt(II) ions was accomplished with a halogen ion such as chloride, bromide, or iodide ion as a pairing ion species for any SLM. The ranking of the permeability of the metallic ions was Cu[sup +,2+], Zn[sup 2+], Cd[sup 2+] [much gt] Pb[sup 2+], Co[sup 2+]. When the oxidation-reduction potential gradient was used as a driving force for metallic ions, the transport of Cu[sup +] ions was higher than those of Cd[sup 2+] and Zn[sup 2+] ions for any SLM containing bathocuproine, neocuproine, or bathophenanthroline. On the other hand, in the transport system which used the concentration gradient of pairing ion species, the permeability of the Cu[sup 2+] ion decreased whereas that of the Cd[sup 2+] ion increased. Moreover, it was found that the different selectivity for the transport of metallic ions is produced by using various pairing ion species. 18 refs., 9 figs.

  4. Conversion of fumaric acid to L-malic by sol-gel immobilized Saccharomyces cerevisiae in a supported liquid membrane bioreactor.

    PubMed

    Bressler, Eyal; Pines, Ophry; Goldberg, Israel; Braun, Sergei

    2002-01-01

    Conversion of fumaric acid (FA) to L-malic acid (LMA) was carried out in a bioreactor divided by two supported liquid membranes (SLMs) into three compartments: Feed, Reaction, and Product. The Feed/Reaction SLM, made of tri-n-octylphosphine oxide (vol 10%) in ethyl acetate, was selective toward the substrate, fumaric acid (S(FA/LMA) = 10). The Reaction/Product SLM, made of di(2-ethylhexyl) phosphate (vol 10%) in dichloromethane, was selective toward the product, L-malic acid (S(LMA/FA) = 680). Immobilized yeast engineered to overproduce the enzyme fumarase [E.C. 4.2.1.2] was placed in the Reaction compartment and served as the catalyst. The yeast was immobilized in small glasslike beads of alginate-silicate sol-gel matrix. The construction of the bioreactor ensured unidirectional flow of the substrate from the Feed to the Reaction and of the product from the Reaction to the Product compartments, with the inorganic counterion traveling in the opposite direction. The conversion of almost 100%, above the equilibrium value of ca. 84% and higher than that for the industrial process, 70%, was achieved. In contrast to the existing industrial biocatalytic process resulting in L-malic acid salts, direct production of the free acid is described. PMID:12052057

  5. Supported liquid membrane extraction coupled in-line to commercial capillary electrophoresis for rapid determination of formate in undiluted blood samples.

    PubMed

    Pantůčková, Pavla; Kubáň, Pavel; Boček, Petr

    2013-07-19

    A cheap, disposable sample pretreatment device with planar supported liquid membrane (SLM) was proposed, assembled and placed into an autosampler carousel of a commercial capillary electrophoresis (CE) instrument for automated pretreatment and analysis of formate in undiluted whole blood and serum samples. All analytical procedures except for filling the pretreatment device with donor and acceptor solutions, i.e., extraction across SLM, injection of the extracted sample and CE-UV determination of formate, were performed fully automatically. The pretreatment device required only μL volumes of blood sample and organic solvent per extraction and was disposed off after each extraction. Good repeatability of peak areas (≤7.7%) and migration times (≤1.5%), linear relationship (r(2)=0.998-0.999) and limits of detection (≤35μM) were achieved. The overall analytical process including blood withdrawal, filling the SLM device with respective solutions, extraction of blood sample, injection into separation capillary and CE separation of formate from other anions took less than 4min. The method was proved useful by direct determination of elevated formate concentrations in undiluted serum samples of a methanol intoxicated patient. Due to its compatibility with currently commercially available CE instrumentation, disposability of extraction devices, minimum sample handling/consumption, and short extraction/analysis times, the developed method might be attractive for rapid diagnosis of methanol poisoning in clinical and toxicological laboratories. PMID:23777836

  6. Liquid level sensing device

    DOEpatents

    Tokarz, Richard D.

    1983-01-01

    A liquid level sensing device comprising a load cell supporting a column or stack of segments freely resting on one another. The density of each element is substantially identical to that of the surrounding liquid. The elements are freely guided within a surrounding tube. As each element is exposed above the liquid level, its weight will be impressed through the column to the load cell, thereby providing a signal at the load cell directly proportional to the liquid level elevation.

  7. A biological method of including mineralized human liquid and solid wastes into the mass exchange of bio-technical life support systems

    NASA Astrophysics Data System (ADS)

    Ushakova, S. A.; Tikhomirov, A. A.; Tikhomirova, N. A.; Kudenko, Yu. A.; Litovka, Yu. A.; Anishchenko, O. V.

    2012-10-01

    The main obstacle to using mineralized human solid and liquid wastes as a source of mineral elements for plants cultivated in bio-technical life support systems (BLSS) is that they contain NaCl. The purpose of this study is to determine whether mineralized human wastes can be used to prepare the nutrient solution for long-duration conveyor cultivation of uneven-aged wheat and Salicornia europaea L. plant community. Human solid and liquid wastes were mineralized by the method of "wet incineration" developed by Yu. Kudenko. They served as a basis for preparing the solutions that were used for conveyor-type cultivation of wheat community represented by 5 age groups, planted with a time interval of 14 days. Wheat was cultivated hydroponically on expanded clay particles. To reduce salt content of the nutrient solution, every two weeks, after wheat was harvested, 12 L of solution was removed from the wheat irrigation tank and used for Salicornia europaea cultivation in water culture in a conveyor mode. The Salicornia community was represented by 2 age groups, planted with a time interval of 14 days. As some portion of the nutrient solution used for wheat cultivation was regularly removed, sodium concentration in the wheat irrigation solution did not exceed 400 mg/L, and mineral elements contained in the removed portion were used for Salicornia cultivation. The experiment lasted 4 months. The total wheat biomass productivity averaged 30.1 g · m-2 · day-1, and the harvest index amounted to 36.8%. The average productivity of Salicornia edible biomass on a dry weight basis was 39.3 g · m-2 · day-1, and its aboveground mass contained at least 20% of NaCl. Thus, the proposed technology of cultivation of wheat and halophyte plant community enables using mineralized human wastes as a basis for preparing nutrient solutions and including NaCl in the mass exchange of the BLSS; moreover, humans are supplied with additional amounts of leafy vegetables.

  8. In silico and in vitro metabolism studies support identification of designer drugs in human urine by liquid chromatography/quadrupole-time-of-flight mass spectrometry.

    PubMed

    Tyrkkö, Elli; Pelander, Anna; Ketola, Raimo A; Ojanperä, Ilkka

    2013-08-01

    Human phase I metabolism of four designer drugs, 2-desoxypipradrol (2-DPMP), 3,4-dimethylmethcathinone (3,4-DMMC), α-pyrrolidinovalerophenone (α-PVP), and methiopropamine (MPA), was studied using in silico and in vitro metabolite prediction. The metabolites were identified in drug abusers’ urine samples using liquid chromatography/quadrupole-time-of-flight mass spectrometry (LC/Q-TOF/MS). The aim of the study was to evaluate the ability of the in silico and in vitro methods to generate the main urinary metabolites found in vivo. Meteor 14.0.0 software (Lhasa Limited) was used for in silico metabolite prediction, and in vitro metabolites were produced in human liver microsomes (HLMs). 2-DPMP was metabolized by hydroxylation, dehydrogenation, and oxidation, resulting in six phase I metabolites. Six metabolites were identified for 3,4-DMMC formed via N-demethylation, reduction, hydroxylation, and oxidation reactions. α-PVP was found to undergo reduction, hydroxylation, dehydrogenation, and oxidation reactions, as well as degradation of the pyrrolidine ring, and seven phase I metabolites were identified. For MPA, the nor-MPA metabolite was detected. Meteor software predicted the main human urinary phase I metabolites of 3,4-DMMC, α-PVP, and MPA and two of the four main metabolites of 2-DPMP. It assisted in the identification of the previously unreported metabolic reactions for α-PVP. Eight of the 12 most abundant in vivo phase I metabolites were detected in the in vitro HLM experiments. In vitro tests serve as material for exploitation of in silico data when an authentic urine sample is not available. In silico and in vitro designer drug metabolism studies with LC/Q-TOF/MS produced sufficient metabolic information to support identification of the parent compound in vivo. PMID:23797910

  9. Liquid Phase Methanol Process Development Unit: installation, operation, and support studies. Technical progress report No. 10, 1 January-31 March 1984

    SciTech Connect

    Not Available

    1984-04-20

    This extremely significant 10th quarter was highlighted by the successful shakedown operation of the LaPorte PDU. Obstacles to start-up, which included exotherms in the unit and the presence of carbonyls, were eliminated. For the successful 10-day PDU shakedown operation, 900 lb of EPJ-19LR catalyst were used. Methanol was produced from both balanced and CO-rich synthesis gas at various operating conditions, and ranged from 1.8 to 8.5 tpd. The highest catalyst productivity achieved during the run was 1.75 lb of methanol/lb catalyst-h, which is significantly higher than can be achieved in gas phase synthesis. Catalyst attrition was significant; the catalyst extrudates in the ebullated-bed reactor rapidly attrited. The catalyst formed an 18 wt % slurry by the end of the run. However, during the transition from ebullated to slurry catalyst, the PDU and catalyst performed very well, and catalyst activity remained high. Support work at CSI continued with autoclave testing of a new catalyst candidate for liquid-entrained operations, and with other miscellaneous tests for hydrodynamic characterization of catalyst powders. At APCI, a 250-h test using an ICI catalyst on balanced gas at a 37 wt % loading was successfully completed in the 300-cc autoclave. The results are very encouraging with respect to maximizing productivity on a reactor volume basis. To complete the data base on catalyst aging, a gas phase activity maintenance run was successfully conducted. The results suggest that CO may be important in catalyst deactivation for gas phase methanol synthesis. 6 references, 32 figures, 28 tables.

  10. Speciation Analysis of Labile and Total Silver(I) in Nanosilver Dispersions and Environmental Waters by Hollow Fiber Supported Liquid Membrane Extraction.

    PubMed

    Chao, Jing-Bo; Zhou, Xiao-Xia; Shen, Mo-Hai; Tan, Zhi-Qiang; Liu, Rui; Yu, Su-Juan; Wang, Xiao-Wei; Liu, Jing-Fu

    2015-12-15

    Hollow fiber supported liquid membrane (HFSLM) extraction was coupled with ICP-MS for speciation analysis of labile Ag(I) and total Ag(I) in dispersions of silver nanoparticles (AgNPs) and environmental waters. Ag(I) in aqueous samples was extracted into the HFSLM of 5%(m/v) tri-n-octylphosphine oxide in n-undecane, and stripped in the acceptor of 10 mM Na2S2O3 and 1 mM Cu(NO3)2 prepared in 5 mM NaH2PO4-Na2HPO4 buffer (pH 7.5). Negligible depletion and exhaustive extraction were conducted under static and 250 rpm shaking to extract the labile Ag(I) and total Ag(I), respectively. The extraction equilibration was reached in 8 h for both extraction modes. The extraction efficiency and detection limit were (2.97 ± 0.25)% and 0.1 μg/L for labile Ag(I), and (82.3 ± 2.0)% and 0.5 μg/L for total Ag(I) detection, respectively. The proposed method was applied to determine labile Ag(I) and total Ag(I) in different sized AgNP dispersions and real environmental waters, with spiked recoveries of total Ag(I) in the range of 74.0-98.1%. With the capability of distinguishing labile and total Ag(I), our method offers a new approach for evaluating the bioavailability and understanding the fate and toxicity of AgNPs in aquatic systems. PMID:26580982

  11. Halophytic plants as a component of a bioregenerative life support system for recycling of NaCl contained in human liquid waste.

    NASA Astrophysics Data System (ADS)

    Balnokin, Yurii; Balnokin, Yurii; Myasoedov, Nikolay; Popova, Larissa; Tikhomirov, Alexander A.; Ushakova, Sofya; Tikhomirova, Natalia; Lasseur, Christophe; Gros, Jean-Bernard

    Currently, the closure of matter turnover is one of the urgent problems of bioregenerative life support system (BLSS) designing. The important aspect of the problem is involving of substances contained in liquid and solid exometabolites of humans inhabiting BLSS into intrasystem matter turnover. Recycling of Na+ and Cl- contained in human liquid exometabolites, i.e. urine is acknowledged to be among the main tasks of the matter turnover in BLSS. The ions excreted with urine may be returned to human organism with food. A way to allow this is including edible halophytic plants into the phototrophic compartment of BLSS. Halophytes are defined as plants which can grow on saline soils and produce high biomass under these conditions. Some halophytes can take up high quantities of Na+ and Cl- and accumulate the ions in the shoots or extrude them to leaf surface by means of salt glands. To allow Na+ and Cl- recycling through halophyte utilization, the following principal steps should be accomplished: (i) mineralization of the exometabolites by physicochemical methods; (ii) oxidation of ammonia formed during the exometabolite mineralization to nitrate by nitrifying bacteria, (iii) growing the halophyte on the nutrient solution prepared on the basis of the mineralized exometabolites, (iv) introducing the halophyte green biomass into human food. The present work is devoted to the following problems: (i) selection of a salt-accumulating/extruding halophytic plant suitable for Na+ and Cl- recycling in BLSS and (ii) parameter evaluation of a plant conveyor containing the halophytic plants at various ages. Halophytic plants selected for BLSS should meet the following criteria: (i) ability to grow under 24-hour-illumination, (ii) high productivity, (iii) ability to accumulate Na+ and Cl- in high quantities in shoots or to excrete salts to leaf surface, (iv) edibility, and (v) high nutritive value of the biomass. Relying on these criteria, salt-accumulating halophyte Salicornia

  12. High-Surface-Area CO2 Sponge: High Performance CO2 Scrubbing Based on Hollow Fiber-Supported Designer Ionic Liquid Sponges

    SciTech Connect

    2010-09-01

    IMPACCT Project: The team from ORNL and Georgia Tech is developing a new technology that will act like a sponge, integrating a new, alcohol-based ionic liquid into hollow fibers (magnified image, right) to capture CO2 from the exhaust produced by coal-fired power plants. Ionic liquids, or salts that exist in liquid form, are promising materials for carbon capture and storage, but their tendency to thicken when combined with CO2 limits their efficiency and poses a challenge for their development as a cost-effective alternative to current-generation solutions. Adding alcohol to the mix limits this tendency to thicken in the presence of CO2 but can also make the liquid more likely to evaporate, which would add significantly to the cost of CO2 capture. To solve this problem, ORNL is developing new classes of ionic liquids with high capacity for absorbing CO2. ORNL’s sponge would reduce the cost associated with the energy that would need to be diverted from power plants to capture CO2 and release it for storage.

  13. Conveyor Cultivation of the Halophytic Plant Salicornia europaea for the Recycling of NaCl from Human Liquid Waste in a Biological Life Support System.

    NASA Astrophysics Data System (ADS)

    Balnokin, Yurii; Myasoedov, Nikolay; Popova, Larissa; Tikhomirov, Alexander A.; Ushakova, Sofya; Tikhomirova, Natalia; Lasseur, Christophe; Gros, Jean-Bernard

    One problem in designing bioregenerative life support systems (BLSS) is developing technolo-gies to include human liquid and solid waste in intrasystem recycling. A specific task is recycling of NaCl excreted in urine by humans. We showed recently that this could be achieved through inclusion of the salt accumulating halophyte Salicornia europaea in the autotrophic compart-ment of the BLSS (Balnokin et al., ASR, 2010, in press). A model of NaCl circulation in BLSS with inclusion of S. europaea was based on the NaCl turnover in the human -urine -nutrient solution -S. europaea -human cycle. Mineralized urine was used as a basis for preparation of a nutrient solution for the halophyte cultivation. The shoots of the halophyte cultivated in the mineralized urine and containing NaCl could to be used by the BLSS inhabitants in their diets. In this report we describe cultivation of S. europaea which allows turnover of NaCl and produces daily shoot biomass containing Na+ and Cl- in quantities approximately equal to those excreted in daily human urine. The plants were grown in water culture in a climatic chamber under controlled conditions. A solution simulating mineralized urine (SSMU) was used as a basis for preparation of a nutri-ent solution for S. europaea cultivation. For continuous biomass production, seedlings of S. europaea, germinated preliminary in moist sand, were being transferred to the nutrient solu-tion at regular intervals (every two days). Duration of the conveyor operation was 112 days. During the first 56 days, the seedlings were being planted in SSMU diluted by a factor of 1.5 (2/3 SSMU). The same solution was introduced into the growth vessels as volumes of growth medium decreased due to plant transpiration. Starting from the 56th day as conveyor operation was initiated, the plants were being harvested every two days; the solutions from the discharged vessels were mixed with the fresh SSMU and the mixture was introduced into all other growth vessels of

  14. Optimization of covalent immobilization of Trichoderma reesei cellulase onto modified ReliZyme HA403 and Sepabeads EC-EP supports for cellulose hydrolysis, in buffer and ionic liquids/buffer media.

    PubMed

    Bilgin, Ramazan; Yalcin, M Serkan; Yildirim, Deniz

    2016-08-01

    The covalent immobilization of Trichoderma reesei cellulase onto modified ReliZyme HA403 and Sepabeads EC-EP supports were carried out. The optimal immobilization conditions were determined using response surface methodology. The hydrolysis of cellulose using the free and immobilized cellulase preparations in ionic liquids (IL) using cosolvents was investigated. The hydrolytic activities in buffer medium containing 25% (v/v) of 1-butyl-3-methylimidazolium hexafluorophosphate were around 2.6-, 1.6-, and 5.5-fold higher than the activities in buffer medium. The retained initial activities were 32% and 57%, respectively for cellulase preparations immobilized onto Sepabeads EC-EP support and onto modified ReliZyme HA403 support after 5 reuses. PMID:25811997

  15. Application of hollow fiber-supported liquid-phase microextraction coupled with HPLC for the determination of guaifenesin enantiomer-protein binding.

    PubMed

    Hatami, Mehdi; Farhadi, Khalil

    2012-07-01

    A hollow fiber liquid-phase microextraction technique coupled with high-performance liquid chromatography with fluorescence detection was employed for determination and evaluation of the binding characteristics of drugs to bovine serum albumin (BSA). Enantiomers of guaifenesin (an expectorant drug) were investigated as a model system. After optimization of some influencing parameters on microextraction, the proposed method was used for calculation of the target drug distribution coefficient between n-octanol and the buffer solution as well as study of drug-BSA binding in physiological conditions. The developed method shows a new, improved and simple procedure for determination of free drug concentration in biological fluids and the extent of drug-protein binding. PMID:22102436

  16. Liquid-phase methanol process development unit: installation, operation, and support studies. Technical progress report No. 2, January 1-March 31, 1982

    SciTech Connect

    Holley, E.P.; Klosek, J.; Spector, I.C.; Mednick, R.L.

    1982-04-20

    Approval was obtained for the unified design concept, advanced schedule for relocation of the LPM pilot plant, and advanced procurement of long lead delivery equipment items. The LaPorte LPMeOH PDU Process Flowsheet was developed further and the Engineering Flowsheet evolved to the Revision OA preliminary issue. Eight cases of point-by-point heat and mass balances were released. Process equipment specifications were issued for 30 of the 32 equipment items. Mechanical specifications were issued for 16 equipment items. Quotations were received for the 2 long lead delivery items, the Feed/Recycle engineeeringompressor and the Slurry Circulation Pumps, technical evaluations of these bids are underway. Semi-final equipment arrangement and plot plan drawings were prepared. The Preliminary Hazards Review was conducted and the subsequent Design Hazards Review was initiated. Progress was made on the specification of the Data Acquisition System. APCI established the priority for compositions of new methanol powder catalysts to be prepared. Construction of the APCI Gas Phase Screening Reactor and Stirred Autoclave Reactor continued on schedule. Progress was made in evaluating the potential modification of the Deckwer liquid phase Fisher-Tropsch model to describe LPMeOH performance. In the CSI laboratories, a 550-hour liquid-fluidized run was completed successfully in the Lab PDU. Preliminary results indicate that the new catalyst tested is more attrition resistant than any prior liquid-fluidized catalyst candidate. Testing of in-situ catalyst reduction procedures continued in the Stirred Autoclave Reactor with successful results which led CSI to file a Record of Invention form for a potential invention covering this process. Specifications and quotations for major equipment items in the CSI liquid-entrained PDU were completed and received.

  17. Liquid-phase methanol process development unit: installation, operation, and support studies. Technical progress report No. 1, 28 September 1981-31 December 1981

    SciTech Connect

    Not Available

    1982-01-20

    During this period the Work Breakdown Structure Dictionary was established. Task 1 was completed with submittal of the Project Work Plan and the Quality Assurance Manual. CSI produced basic process design information and a preliminary flowsheet for the LaPorte LPMeOH PDU. APCI developed the flowsheet further and set up the process on APCI's process simulator. The flowsheet development revealed a number of major changes necessary in the existing LPM pilot plant; this has led to pursuit of a unified design concept. Approval was requested for the unified design concept as well as advanced schedule for relocation of the LPM unit and advanced procurement of long delivery equipment items. A number of preliminary heat and material balances were calculated for the LPMeOH PDU and preliminary process specifications were prepared for the equipment items. The final design basis was established. The design pressure was set at 1000 psig. Eight design operating cases were defined for the following range of reactor operating conditions: Pressure - 500 to 900 psig, Temperature - 220 to 270/sup 0/C, Liquid-Fluidized Space Velocity - 1000 to 4000 l/hr-kg catalyst, Liquid-Entrained Space Velocity - 2000 to 10,000 l/hr-kg catalyst, and Liquid-Entrained Catalyst Loading - 0.1 to 0.4 kg catalyst/l oil. The methanol production rate for these cases ranges from 0.2 to 9.7 short tons per day. Preliminary equipment arrangement and site layout drawings were prepared for the PDU. In the laboratories, CSI began autoclave testing of in-situ catalyst reduction procedures. The specification and evaluation of equipment for the CSI laboratory PDU progressed. CSI prepared and issued a Topical Report covering liquid-entrained LPMeOH lab development work accomplished under advance funding. APCI's laboratories progressed with the design of the bench scale slurry reactor.

  18. Liquid Sloshing Dynamics

    NASA Astrophysics Data System (ADS)

    Ibrahim, Raouf A.

    2005-06-01

    The problem of liquid sloshing in moving or stationary containers remains of great concern to aerospace, civil, and nuclear engineers; physicists; designers of road tankers and ship tankers; and mathematicians. Beginning with the fundamentals of liquid sloshing theory, this book takes the reader systematically from basic theory to advanced analytical and experimental results in a self-contained and coherent format. The book is divided into four sections. Part I deals with the theory of linear liquid sloshing dynamics; Part II addresses the nonlinear theory of liquid sloshing dynamics, Faraday waves, and sloshing impacts; Part III presents the problem of linear and nonlinear interaction of liquid sloshing dynamics with elastic containers and supported structures; and Part IV considers the fluid dynamics in spinning containers and microgravity sloshing. This book will be invaluable to researchers and graduate students in mechanical and aeronautical engineering, designers of liquid containers, and applied mathematicians.

  19. Liquid-phase-methanol process-development unit: installation, operation, and support studies. Technical progress report No. 5, 1 October 1982-31 December 1982

    SciTech Connect

    Not Available

    1983-01-20

    This report covers the fifth period of Contract performance. The overall objective of this program is to demonstrate the technical feasibility of the Liquid Phase Methanol (LPMeOH) process at theProcess Development Unit (PDU) scale of operation. Revision 2 of the LaPorte LPMeOH Process Development Unit (PDU) Engineering Flowsheet was released, incorporating advances made in the engineering design. The APCI Hazards Review team continued assessing risks associated with various process systems, particularly the reactor slurry loop. Process specifications were issued for an iron carbonyl removal system on the basis of a survey of industrial experience and literature related to the subject. The design for a flare system was developed APCI prepared an outline of catalyst reduction procdures, and data was accumulated on properties of circulating oils and slurry. A literature search was completed by CSI for the major topics of interest to the program. In CSI's laboratory, successful testing of in-situ catalyst reduction procedures continued in the CSI Stirred Autoclave Reactors, and two additional commercial catalysts were screened. The Laboratory PDU modifications continue on schedule. Further anlaysis of the 540-hour liquid-fluidized run in the CSI Laboratory PDU was completed. To assist in fundamantal modeling studies, an experimental program to generate bed expansion and gas holdup data in the CSI liquid-fluidized PDU reactor was completed. APCI reviewed chemical equilibrium correlations for the methanol synthesis reaction verified the validity of literature correlations at LPMeOH reaction conditions. The APCI backflow cell reactor computer model, to aid in scale-up of reactor design, was completed and the Continuous stirred Tank Reactor (CSTR) analysis and simulation program was used for determination of kinetics for the LPMeOH process.

  20. Clustering effects of GM1 and formation mechanisms of interdigitated liquid disordered domains in GM1/SM/CHOL-supported planar bilayers on mica surfaces

    NASA Astrophysics Data System (ADS)

    Shang, Zhiguo; Mao, Yanli; Tero, Ryugo; Liu, Xinli; Hoshino, Tyuji; Tanaka, Motohiko; Urisu, Tsuneo

    2010-09-01

    We have observed by atomic force microscopy that an interdigitated liquid disordered domain (ILDD) is formed in the ganglioside (GM1)/sphingomyelin (SM)/cholesterol (CHOL) bilayers on a mica surface and accelerates the formation of fibriller Aβ agglomerates. By studies of the mechanisms using molecular dynamics simulations, we conclude that the ILDD structure is formed as a result of the phase separation to SM- and GM1-rich domains on the mica surface induced by the effects of GM1 clustering and the interaction between the GM1 head group and the water layer adsorbed in the ditrigonal cavity on the mica surface.

  1. Liquid-phase methanol process-development unit: installation, operation, and support studies. Technical progress report No. 6, 1 January 1983-31 March 1983

    SciTech Connect

    Not Available

    1983-04-20

    Experiments confirmed the need for iron carbonyl removal equipment, and bids on these items were evaluated. Equipment procurement for the LaPorte PDU has been completed, with the exception of iron carbonyl removal equipment. On 13 January, several technical redirections were proposed to DOE. In reactor modeling, APCI completed a study of the significance of mass transfer and equilibrium constraints on CSI advance funded data. The results suggest that this data is difficult to use for evaluating kinetics. The backflow reactor model was modified. At CSI, all equipment for the analytical portion of the DEC/AIM data acquisition system for LaPorte has been received. In the CSI autoclave, optimization of catalyst reduction procedures continued. Four liquid-entrained commercial catalysts were evaluated. An attrition test unit was constructed and testing of liquid-fluidized catalyst attrition has begun under methanol synthesis conditions. Modifications of the CSI Lab PDU are about 95% complete. APCI signed a contract with Hydrocarbon Research, Inc. (HRI) for cold-flow studies of the ebullated bed reactor design.

  2. Ionic liquid supported on an electrodeposited polycarbazole film for the headspace solid-phase microextraction and gas chromatography determination of aromatic esters.

    PubMed

    Feng, Yuanyuan; Zhao, Faqiong; Zeng, Baizhao

    2015-05-01

    A polycarbazole film was electrodeposited on a stainless-steel wire from a solution of N,N-dimethylformamide/propylene carbonate (1:9 v/v) containing 0.10 M carbazole and 0.10 M tetrabutylammonium perchlorate. The obtained polycarbazole fiber was immersed into an ionic liquid (1-hydroxyethyl-3-methyl imidazolium bis[(trifluoromethyl)sulfonyl]imide) solution (in dimethylsulfoxide) for 30 min, followed by drying under an infrared lamp. The resulting polycarbazole/ionic liquid fiber was applied to the headspace solid-phase microextraction and determination of aromatic esters by coupling with gas chromatography and flame ionization detection. Under the optimized conditions, the limits of detection were below 61 ng/L (S/N = 3) and the linear ranges were 0.061-500 μg/L with correlation coefficients above 0.9876. The relative standard deviations were below 4.8% (n = 5) for a single fiber, and below 9.9% for multi-fiber (n = 4). This fiber also exhibited good stability. It could be used for more than 160 times of headspace solid-phase microextraction and could withstand a high temperature up to 350°C. PMID:25676087

  3. An Improved Method for the Separation of Lead-210 from Ra-DEF for Radioactive Equilibrium Experiments: Microscale Liquid-Liquid Extraction Using a Polymer-Supported Crown Ether

    NASA Astrophysics Data System (ADS)

    Dietz, Mark L.; Horwitz, E. Philip

    1996-02-01

    A novel extraction chromatographic material, comprised of a solution of a lead-selective macrocyclic polyether (di-t-butylcyclohexano-18-crown-6) in isodecanol sorbed on an inert polymeric support, is shown to provide a rapid and simple means for the separation of lead-210 from its daughter products for subsequent radiochemical experimentation.

  4. 3D-printed polylactic acid supports for enhanced ionization efficiency in desorption electrospray mass spectrometry analysis of liquid and gel samples.

    PubMed

    Elviri, Lisa; Foresti, Ruben; Bianchera, Annalisa; Silvestri, Marco; Bettini, Ruggero

    2016-08-01

    The potential of 3D printing technology was here exploited to prepare tailored polylactic acid (PLA) supports for desorption electrospray ionization (DESI) experiments. PLA rough solid supports presenting wells of different shape (i.e. cylindrical, cubic and hemispherical cavities) were designed to accommodate samples of different physical state. The potentials of such supports in terms of sample loading capacity, sensitivity, signal stability were tested by analysing a peptide (i.e. insulin) and an aminoglycoside antibiotic (i.e. gentamicin sulphate) from solution and a chitosan-based gel. The results obtained were compared with those obtained by using a traditional polytetrafluoroethylene (PTFE) support and discussed. By using PLA support on the flat side, signal intensity improved almost twice with respect to PTFE support, whereas with spherical wells a five times improved signal sensitivity and good stability (RSD<6%) were obtained for the analysis of two model molecules. Limits of detection were in the 3-10nM range and linearity was demonstrated for both analytes in the 0.05-0.5μM range for semi-quantitative or quantitative purposes. The use of a well and the set-up of optimal source parameters allowed the analysis of samples in a gel state with good precision (RSD<10%) and accuracy (86±6-102±9%), otherwise difficult to analyse on a flat smooth surface. These findings are of great interest and stimulus to exploit the advantages of 3D printing technology for the development of devices for a DESI source, presenting different shapes or configuration as a function of the sample types. PMID:27216689

  5. Experimental evidence supporting the insensitivity of cloud droplet formation to the mass accommodation coefficient for condensation of water vapor to liquid water

    NASA Astrophysics Data System (ADS)

    Langridge, Justin M.; Richardson, Mathews S.; Lack, Daniel A.; Murphy, Daniel M.

    2016-06-01

    The mass accommodation coefficient for uptake of water vapor to liquid water, αM, has been constrained using photoacoustic measurements of aqueous absorbing aerosol. Measurements performed over a range of relative humidities and pressures were compared to detailed model calculations treating coupled heat and mass transfer occurring during photoacoustic laser heating cycles. The strengths and weaknesses of this technique are very different to those for droplet growth/evaporation experiments that have typically been applied to these measurements, making this a useful complement to existing studies. Our measurements provide robust evidence that αM is greater than 0.1 for all humidities tested and greater than 0.3 for data obtained at relative humidities greater than 88% where the aerosol surface was most like pure water. These values of αM are above the threshold at which kinetic limitations are expected to impact the activation and growth of aerosol particles in warm cloud formation.

  6. Laboratory characterization of non-aqueous phase liquid/tracer interaction in support of a vadose zone partitioning interwell tracer test

    NASA Astrophysics Data System (ADS)

    Deeds, Neil E.; McKinney, Daene C.; Pope, Gary A.

    2000-01-01

    Contaminant characterization is important for successful remediation of non-aqueous phase liquids (NAPLs) in the unsaturated zone. A partitioning interwell tracer test (PITT) can provide a good estimate of average subsurface NAPL saturations. Screening experiments were completed in the laboratory to evaluate several gas tracers for a PITT study to be completed in the vadose zone at Kirtland Air Force Base in Albuquerque, NM. Four perfluorocarbon tracers were found to be suitable for this PITT. Further laboratory column studies were completed using contaminated field soil to measure the partition coefficients between the tracers and the NAPL. The results from the column studies showed that the air/NAPL tracer partition coefficients ranged from 8.8±0.6 to 71±3. This range of partition coefficients is suitable for detection of NAPL saturations in the field of 0.002 to 0.14.

  7. HANFORD DOUBLE SHELL TANK (DST) THERMAL & SEISMIC PROJECT SEISMIC ANALYSIS IN SUPPORT OF INCREASED LIQUID LEVEL IN 241-AP TANK FARMS

    SciTech Connect

    MACKEY TC; ABBOTT FG; CARPENTER BG; RINKER MW

    2007-02-16

    The overall scope of the project is to complete an up-to-date comprehensive analysis of record of the DST System at Hanford. The "Double-Shell Tank (DST) Integrity Project - DST Thermal and Seismic Project" is in support of Tri-Party Agreement Milestone M-48-14.

  8. Interionic Interactions in Imidazolium-Based Ionic Liquids: The Role of the C2-Position Revealed by Raman Scattering and Supported by IR and NMR Spectroscopy

    NASA Astrophysics Data System (ADS)

    Noack, Kristina; Paape, Natalia; Kiefer, Johannes; Wasserscheid, Peter; Leipertz, Alfred

    2010-08-01

    Intermolecular interactions determine the state of aggregation of a substance at given temperature. Based on that, changes in intermolecular interactions can lead to microscopic reordering which may be observed macroscopically in terms of altered physicochemical properties. Especially, when chemicals are employed in technical processes, it is important to control and regulate their properties to guarantee product quality. A special group of chemical substances increasingly gaining interest in the field of chemical and process engineering are room temperature ionic liquids (RTILs). In general, RTILs are organic salts with melting points "below the boiling point of water". The variety of possible combinations of cations and anions lead to a wide range of chemical and thermo-physical properties. In fact, it is possible to tune their properties by adjusting the ratio of Coulomb and van der Waals interactions. However, because it is hardly possible to investigate a reasonable fraction of the potential cation-anion combinations, a molecular-based understanding of their properties is crucial to make a rational design possible. In this regard vibrational spectroscopy has proven to be very beneficial for structural analysis and the investigation of interionic and intermolecular interactions. Therein, especially Raman spectroscopy shows a significant advantage of being insensitive to water interference and it is widely applied in the field of ionic liquids. Among others the 1-alkyl-3-methylimidazolium [RMIM] based ILs have been employed as model ILs in structural analysis, and most vibrational studies available in literature have been carried out investigating this kind of ILs. In contrast, spectroscopic data and calculations of C2-methylated 1,2-dialkyl-3-methylimidazolium based ILs, are available to a much lesser extend. The substitution in the C2 position in those ILs disrupts the main hydrogen-bonding interaction between the cation and the anion and is expected to lead

  9. Liquid phase methanol LaPorte process development unit: Modification operation, and support studies. Task 3.6/3.7: Alternative catalyst/life run

    SciTech Connect

    Not Available

    1991-01-28

    In April 1987, Air Products started the third and final contract with the US Department of Energy to develop the Liquid Phase Methanol (LPMEOH) process. One of the objectives was to identify alternative commercial catalyst(s) for the process. This objective was strategically important as we want to demonstrate that the LPMEOH process is flexible and not catalyst selection limited. Among three commercially available catalysts evaluated in the lab, the catalyst with a designation of F21/0E75-43 was the most promising candidate. The initial judging criteria included not only the intrinsic catalyst activity but also the ability to be used effectively in a slurry reactor. The catalyst was then advanced for a 40-day life test in a laboratory 300 cc autoclave. The life test result also revealed superior stability when compared with that of a standard catalyst. Consequently, the new catalyst was recommended for demonstration in the Process Development Unit (PDU) at LaPorte, Texas. This report details the methodology of testing and selecting the catalyst.

  10. Reaction profiling by ultra high-pressure liquid chromatography/time-of-flight mass spectrometry in support of the synthesis of DNA-encoded libraries.

    PubMed

    Hargiss, Leonard O; Zipp, G Greg; Jessop, Theodore C; Sun, Xuejun; Keyes, Philip; Rawlins, David B; Liang, Zhi; Park, Kum Joo; Gu, Huizhong

    2014-11-15

    An ultra high-pressure liquid chromatography/mass spectrometry (UHPLC/MS) separation and analysis method has been devised for open access analysis of synthetic reactions used in the production of DNA-encoded chemical libraries. The aqueous mobile phase is 100mM hexafluoroisopropanol and 8.6mM triethylamine; the organic mobile phase is methanol. The UHPLC separation uses a C18 OST column (50mm×2.1mm×1.7μm) at 60°C, with a flow rate of 0.6mL/min. Gradient concentration is from 10 to 40% B in 1.0min, increasing to 95% B at 1.2min. Cycle time was about 5min. This method provides a detection limit of a 20-mer oligonucleotide by mass spectrometry of better than 1pmol on-column. Linear UV response for 20-mer extends from 2 to 200pmol/μL in concentration, same-day relative average deviations are less than 5% and bias (observed minus expected) is less than 10%. Deconvoluted mass spectra are generated for components in the predicted mass range using a maximum entropy algorithm. Mass accuracy of deconvoluted spectra is typically 20ppm or better for isotopomers of oligonucleotides up to 7000Da. PMID:25282130

  11. Effect of content of chiral selector and pore size of core-shell type silica support on the performance of amylose tris(3,5-dimethylphenylcarbamate)-based chiral stationary phases in nano-liquid chromatography and capillary electrochromatography.

    PubMed

    Rocchi, Silvia; Fanali, Salvatore; Farkas, Tivadar; Chankvetadze, Bezhan

    2014-10-10

    In this study the separation performance of various chiral stationary phases (CSPs) made of polysaccharide-based chiral selectors coated onto superficially porous (core-shell or fused-core) silica supports were evaluated. The CSPs obtained by coating of various amounts of chiral selector (1-5%) onto supports of various pore size (100 and 300 Å) were studied. Their evaluation was pursued in both chiral nano-liquid chromatography (nano-LC) and chiral capillary electrochromatography (CEC). Among the goals of this study was to re-examine our previous unexpected finding of better performance of superficially porous CSP under CEC conditions compared to nano-LC conditions for a new set of chiral compounds, as well as to study the effect of varying the chiral selector content and nominal pore size of supporting silica on the performance of core-shell silica-based polysaccharide-type CSPs. Based on the results of this study it can be seen that CSPs based on superficially porous silica can successfully be used for the separation of enantiomers in both nano-LC and CEC mode. Only a slight advantage of CEC over nano-LC mode was observed in this study from the viewpoint of plate numbers, especially at higher mobile phase flow rates. It must also be noted that the optimal theoretical plate height is still too high and further optimization of superficially porous CSPs is necessary for both nano-LC and CEC applications. PMID:24908153

  12. Ultrasound-assisted ionic liquid-based microextraction combined with least squares support vector machines regression for the simultaneous determination of aluminum, gallium, and indium in water and coal samples.

    PubMed

    Ghasemi, Jahan B; Zolfonoun, Ehsan

    2012-06-01

    A new simple and rapid ultrasound-assisted ionic liquid-based microextraction method was applied to preconcentrate aluminum(III), gallium(III), and indium(III) ions from water samples as a prior step to their simultaneous spectrophotometric determination using least squares support vector machines regression. In the novel procedure, 1-hexyl-3-methylimidazolium hexafluorophosphate [C(6)MIM][PF(6)] was dispersed into the aqueous sample solution as fine droplets by ultrasonication, and the analytes were extracted into the ionic liquid phase after complexation with 1,2,5,8-tetrahydroxy anthraquinone (quinalizarine). After centrifuging, the fine droplets of extractant phase were settled to the bottom of the conical-bottom glass centrifuge tube. The detection limits for Al(III), Ga(III), and In(III) were 1.70, 2.02, and 2.06 ng mL(-1), respectively. The precision of the method, evaluated as the relative standard deviation obtained by analyzing a series of ten replicates, was below 3.2% for all elements. The method was successfully applied for the determination of Al(III), Ga(III), and In(III) in real samples. PMID:21789531

  13. Liquid membrane extraction of cadmium

    SciTech Connect

    Berends, A.M.; Breembroek, G.R.M.; Witkamp, G.J.; Rosmalen, G.M van

    1996-12-31

    Three Liquid Membrane extraction designs are compared by their experimental extraction performance of cadmium ions from an aqueous phase with tri-laurylamine dissolved in an aliphatic kerosene. The compared designs are Emulsion Liquid Membrane (ELM), Flat Sheet Supported Liquid Membrane (FSSLM) and Hollow Fiber Supported Liquid Membrane (HFSLM4) extraction units. The results demonstrated that ELM possesses the best extraction performance per volume of equipment, but that HFSLM is a good alternative because of its less complicated design and greater flexibility. 2 refs., 7 figs.

  14. Liquid film target impingement scrubber

    DOEpatents

    McDowell, William J.; Coleman, Charles F.

    1977-03-15

    An improved liquid film impingement scrubber is provided wherein particulates suspended in a gas are removed by jetting the particle-containing gas onto a relatively small thin liquid layer impingement target surface. The impingement target is in the form of a porous material which allows a suitable contacting liquid from a pressurized chamber to exude therethrough to form a thin liquid film target surface. The gas-supported particles collected by impingement of the gas on the target are continuously removed and flushed from the system by the liquid flow through each of a number of pores in the target.

  15. Evaluation of the measurement of Cu(II) bioavailability in complex aqueous media using a hollow-fiber supported liquid membrane device (HFSLM) and two microalgae species (Pseudokirchneriella subcapitata and Scenedesmus acutus).

    PubMed

    Rodríguez-Morales, Erik A; Rodríguez de San Miguel, Eduardo; de Gyves, Josefina

    2015-11-01

    The environmental bioavailability of copper was determined using a hollow-fiber supported liquid membrane (HFSLM) device as a chemical surrogate and two microalgae species (Scenedesmus acutus and Pseudokirchneriella subcapitata). Several experimental conditions were studied: pH, the presence of organic matter, inorganic anions, and concomitant cations. The results indicated a strong relationship between the response given by the HFSLM and the microalgae species with free copper concentrations measured by an ion selective electrode (ISE), in accordance with the free-ion activity model (FIAM). A significant positive correlation was evident when comparing the bioavailability results measured by the HFSLM and the S. acutus microalga species, showing that the synthetic device may emulate biological uptake and, consequently, be used as a chemical test for bioavailability measurements using this alga as a biological reference. PMID:26431807

  16. A supported liquid extraction-LC-MS/MS method for determination of GDC-0980 (Apitolisib), a dual small-molecule inhibitor of class 1A phosphoinositide 3-kinase and mammalian target of rapamycin, in human plasma.

    PubMed

    Ding, X; Li, F; McKnight, J; Schmidt, C; Strooisma, K; Shimizu, H; Faber, K; Ware, J A; Dean, B

    2014-11-01

    A liquid chromatographic-tandem mass spectrometry (LC-MS/MS) method for the determination of GDC-0980 (Apitolisib) concentrations in human plasma has been developed and validated to support clinical development. Supported liquid extraction (SLE) was used to extract plasma samples (80μL) and the resulting samples were analyzed using reverse-phase chromatography and mass spectrometry coupled with a turbo-ionspray interface. The mass analysis of GDC-0980 was performed using multiple reaction monitoring (MRM) transitions in positive ionization mode. The method was validated over the calibration curve range 0.0500-25.0ng/mL using linear regression and 1/x(2) weighting. Within-run relative standard deviation (%RSD) ranged from 0.4 to 3.9%, while the between-run %RSD varied from 1.1 to 1.5% for QCs. The accuracy ranged from 96.1% to 106.7% of nominal for within-run and 96.7-106.7% of nominal for between-run at all concentrations including the LLOQ quality control at 0.0500ng/mL. Extraction recovery of GDC-0980 was between 72.4% and 75.5%. Stability of GDC-0980 was established in human plasma for 547 days at -20°C and -70°C and established in reconstituted sample extracts for 146h when stored at 2-8°C. Stable-labeled internal standard was used to minimize matrix effects. Mean pharmacokinetic parameters determined using this method for the day 1 control group in a phase I trial were: Cmax=11.1ng/mL, AUC0-inf=108ngh/mL, and T1/2=13.1h. PMID:25165011

  17. Supported liquid extraction (SLE) for the analysis of methylamphetamine, methylenedioxymethylamphetamine and delta-9-tetrahydrocannabinol in oral fluid and blood of drivers.

    PubMed

    Rositano, Joanna; Harpas, Peter; Kostakis, Chris; Scott, Timothy

    2016-08-01

    matrix effects were 1.0, 0.97 and 0.78 in DDS buffer and 0.96, 0.96 and 0.62 in blood for MA, MDMA and THC, respectively. Linearity was achieved up to 1250ng/mL for MA and MDMA, and 112ng/mL for THC (r(2)>0.999 for all analytes). The method is designed for easy transfer to an automated liquid handling platform. PMID:26878366

  18. Liquid metal pump

    DOEpatents

    Pennell, William E.

    1982-01-01

    The liquid metal pump comprises floating seal rings and attachment of the pump diffuser to the pump bowl for isolating structural deflections from the pump shaft bearings. The seal rings also eliminate precision machining on large assemblies by eliminating the need for a close tolerance fit between the mounting surfaces of the pump and the seals. The liquid metal pump also comprises a shaft support structure that is isolated from the pump housing for better preservation of alignment of shaft bearings. The shaft support structure also allows for complete removal of pump internals for inspection and repair.

  19. Solar liquid heating system

    SciTech Connect

    Finn, D.J.

    1990-05-08

    This patent describes a solar heater for heating liquids. It comprises: a heatable bag, a support means supporting the heatable bag, a heatable body of liquid in the heatable bag, the heatable bag being disposed in sunlight so as to become heated thereby, a topside gas bag above the heatable bag, the topside gas bag containing a gas for serving as insulation, a topside fluid bag disposed above the topside gas bag and containing a fluid for further insulation. The bags being substantially gasproof and waterproof and also being flexible whereby the gravity pull on the bags and the flexibility thereof causes the upper sides of the bags to seek horizontal levels.

  20. Assessing the feasibility of involving gaseous products resulting from physicochemical oxidation of human liquid and solid wastes in the cycling of a bio-technical life support system

    NASA Astrophysics Data System (ADS)

    Tikhomirov, Alexander; Kudenko, Yurii; Trifonov, Sergey; Ushakova, Sofya

    2012-01-01

    The study addresses the possible ways of involving gaseous products produced by "wet" incineration of human wastes mixed with H2O2 in an alternating electric field in the cycling of the physical model of a bio-technical life support system (BTLSS). The resulting gas mixture contains CO2 and O2, which are easily involved in the cycling in the closed ecosystem, and NH3, which is unacceptable in the atmosphere of the BTLSS. NH3 fixation has been proposed, which is followed by nitrification and involvement of the resulting products in the mass exchange of the closed system. Experiments have been performed to show that plants can be grown in the atmosphere resulting from the closing of the gas loop that includes a physicochemical installation and a growth chamber with plants representing the phototrophic compartment of the BTLSS. The results of the study suggest the conclusion that the proposed method of organic waste oxidation can be a useful tool in creating a physical model of a closed-loop integrated BTLSS.

  1. Dynamic ultrasound-assisted extraction coupled on-line with solid support derivatization and high-performance liquid chromatography for the determination of formaldehyde in textiles.

    PubMed

    Chen, Ligang; Jin, Haiyan; Wang, Liguang; Sun, Lei; Xu, Haoyan; Ding, Lan; Yu, Aimin; Zhang, Hanqi

    2008-05-23

    An on-line method was developed for the extraction, derivatization and determination of formaldehyde in textile samples. Formaldehyde was first extracted with water by ultrasound assisted, and directly introduced into a derivatization column which was packed with a moderately sulfonated cation-exchange resin. The resin used as solid support for the derivatization was charged with 2,4-dinitrophenylhydrazine (DNPH) previously. The formaldehyde DNPH derivative was eluted with the chromatographic mobile phase into an analytical column for the separation, and then monitored by UV detector. The maximum extraction yield was achieved when the extraction vessel was located at 10mm from the ultrasonic source and 10mg textile sample was extracted with 5mL pure water at a flow rate of 1.0mLmin(-1) at 50 degrees C. The detection limit of the proposed method was 0.06mgkg(-1). This method was applied to the determination of formaldehyde in different textile samples, and compared with the state standard method (off-line spectrophotometry) used in China. The similar contents of formaldehyde were obtained for most samples by the two methods, but little higher for some samples obtained by the proposed method. The average relative standard deviation (RSD) obtained by the on-line method was 3.2% which is lower than 29.5% obtained by the standard method. PMID:18378258

  2. Spreading of miscible liquids

    NASA Astrophysics Data System (ADS)

    Walls, Daniel J.; Haward, Simon J.; Shen, Amy Q.; Fuller, Gerald G.

    2016-05-01

    Miscible liquids commonly contact one another in natural and technological situations, often in the proximity of a solid substrate. In the scenario where a drop of one liquid finds itself on a solid surface and immersed within a second, miscible liquid, it will spread spontaneously across the surface. We show experimental findings of the spreading of sessile drops in miscible environments that have distinctly different shape evolution and power-law dynamics from sessile drops that spread in immiscible environments, which have been reported previously. We develop a characteristic time to scale radial data of the spreading sessile drops based on a drainage flow due to gravity. This time scale is effective for a homologous subset of the liquids studied. However, it has limitations when applied to significantly chemically different, yet miscible, liquid pairings; we postulate that the surface energies between each liquid and the solid surface becomes important for this other subset of the liquids studied. Initial experiments performed with pendant drops in miscible environments support the drainage flow observed in the sessile drop systems.

  3. LIQUID-LIQUID EXTRACTION COLUMNS

    DOEpatents

    Thornton, J.D.

    1957-12-31

    This patent relates to liquid-liquid extraction columns having a means for pulsing the liquid in the column to give it an oscillatory up and down movement, and consists of a packed column, an inlet pipe for the dispersed liquid phase and an outlet pipe for the continuous liquid phase located in the direct communication with the liquid in the lower part of said column, an inlet pipe for the continuous liquid phase and an outlet pipe for the dispersed liquid phase located in direct communication with the liquid in the upper part of said column, a tube having one end communicating with liquid in the lower part of said column and having its upper end located above the level of said outlet pipe for the dispersed phase, and a piston and cylinder connected to the upper end of said tube for applying a pulsating pneumatic pressure to the surface of the liquid in said tube so that said surface rises and falls in said tube.

  4. EXPERIMENTAL LIQUID METAL FUEL REACTOR

    DOEpatents

    Happell, J.J.; Thomas, G.R.; Denise, R.P.; Bunts, J.L. Jr.

    1962-01-23

    A liquid metal fuel nuclear fission reactor is designed in which the fissionable material is dissolved or suspended in a liquid metal moderator and coolant. The liquid suspension flows into a chamber in which a critical amount of fissionable material is obtained. The fluid leaves the chamber and the heat of fission is extracted for power or other utilization. The improvement is in the support arrangement for a segrnented graphite core to permit dif ferential thermal expansion, effective sealing between main and blanket liquid metal flows, and avoidance of excessive stress development in the graphite segments. (AEC)

  5. Efficient transport of Am(III) from nitric acid medium using a new conformationally constrained (N,N,N',N'-tetra-2-ethylhexyl)7-oxabicyclo[2.2.1]heptane-2,3-dicarboxamide across a supported liquid membrane.

    PubMed

    Sharma, S; Panja, S; Ghosh, S K; Dhami, P S; Gandhi, P M

    2016-03-15

    Am(III) is one of the most hazardous radionuclide present in nuclear fuel cycle. A new conformationally constrained diamide, (N,N,N',N'-tetra-2-ethylhexyl)7-oxabicyclo[2.2.1]heptane-2,3-dicarboxamide (OBDA) was studied for Am(III) transport from HNO3 medium across a Supported Liquid Membrane. Transport rate was observed to be significantly fast with ∼95% transport of Am(III) within 1h using 0.1M OBDA in the presence of 15% isodecyl alcohol (IDA)/n-dodecane as carrier. The mechanism of transport was investigated by studying various parameters like feed HNO3/NaNO3 concentration, OBDA concentration in the membrane, membrane pore size, membrane thickness etc. From these studies, the mechanism of transport was found to be diffusion controlled with diffusion co-efficient value of 5.1×10(-6)cm(2)/s. The membrane was found to be highly selective for tri- and tetra-valent actinides, and trivalent lanthanides. OBDA based membrane was found to be stable for at least for ten consecutive cycles of operation. PMID:26685064

  6. LIQUID TARGET

    DOEpatents

    Martin, M.D.; Salsig, W.W. Jr.

    1959-01-13

    A liquid handling apparatus is presented for a liquid material which is to be irradiated. The apparatus consists essentially of a reservoir for the liquid, a target element, a drain tank and a drain lock chamber. The target is in the form of a looped tube, the upper end of which is adapted to be disposed in a beam of atomic particles. The lower end of the target tube is in communication with the liquid in the reservoir and a means is provided to continuously circulate the liquid material to be irradiated through the target tube. Means to heat the reservoir tank is provided in the event that a metal is to be used as the target material. The apparatus is provided with suitable valves and shielding to provide maximum safety in operation.

  7. A study of liquid propellant autoignition

    NASA Technical Reports Server (NTRS)

    Lester, D. H.; Gibbs, A. G.; Lessor, D. L.

    1975-01-01

    Data and theory pertinent to the autoignition of liquid oxygen/liquid hydrogen and liquid oxygen propellants were reviewed. Physical models of the processes supporting or contributing to autoignition were developed. Emphasis was placed on the description of the physical environment and its relationship to the autoignition phenomenon.

  8. Liquid atomization

    NASA Astrophysics Data System (ADS)

    Bayvel, L.; Orzechowski, Z.

    The present text defines the physical processes of liquid atomization, the primary types of atomizers and their design, and ways of measuring spray characteristics; it also presents experimental investigation results on atomizers and illustrative applications for them. Attention is given to the macrostructural and microstructural parameters of atomized liquids; swirl, pneumatic, and rotary atomizers; and optical drop sizing methods, with emphasis on nonintrusive optical methods.

  9. Sulfur poisoning of CeO[subscript 2]-Al[subscript 2]O[subscript 3]-supported mono- and bi-metallic Ni and Rh catalysts in steam reforming of liquid hydrocarbons at low and high temperatures

    SciTech Connect

    Xie, Chao; Chen, Yongsheng; Li, Yan; Wang, Xiaoxing; Song, Chunshan

    2010-12-01

    In order to develop a better understanding on sulfur poisoning of reforming catalysts in fuel processing for hydrogen production, steam reforming of liquid hydrocarbons was performed over CeO{sub 2}-Al{sub 2}O{sub 3} supported monometallic Ni and Rh and bimetallic Rh-Ni catalysts at 550 and 800 C. XANES was used to identify the sulfur species in the used catalysts and to study their impacts on the metal surface properties probed by XPS. It was found that both monometallic catalysts rapidly deactivated at 550 C, and showed poor sulfur tolerance. Although ineffective for the Ni catalyst, increasing the temperature to 800 C dramatically improved the sulfur tolerance of the Rh catalyst. XANES revealed that metal sulfide and organic sulfide are the dominant sulfur species on the used Ni catalyst, while sulfonate and sulfate predominate on the used Rh catalyst. The presence of sulfur induced severe carbon deposition on the Ni catalyst at 800 C. The superior sulfur tolerance of the Rh catalyst at 800 C may be associated with its capability in sulfur oxidation. It is likely that the formation of the oxygen-shielded sulfur structure of sulfonate and sulfate can suppress the poisoning impact of sulfur on Rh by inhibiting direct rhodium-sulfur interaction. Moreover, XPS indicated that the metal surface properties of the Rh catalysts after the reaction without and with sulfur at 800 C are similar, suggesting that sulfur poisoning on Rh was mitigated under the high-temperature condition. Although the Rh-Ni catalyst exhibited better sulfur tolerance than the monometallic catalysts at 550 C, its catalytic performance was inferior compared with the Rh catalyst in the sulfur-containing reaction at 800 C probably due to the severe carbon deposition on the bimetallic catalyst.

  10. Characteristics of Liquid Flow Induced by Atmospheric Pressure DC Glow Discharge with Liquid Electrode

    NASA Astrophysics Data System (ADS)

    Tochikubo, Fumiyoshi; Aoki, Takuya; Shirai, Naoki; Uchida, Satoshi

    2015-09-01

    In the application of atmospheric-pressure discharges in contact with liquid, primary reactions are initiated between radicals and liquid molecules at plasma-liquid interface. Since the diffusion in the liquid is very slow, some convective flow is necessary to exchange the chemicals at the plasma-liquid interface for the efficient reactions. In our previous work, we found the appearance of specific downward flow in the liquid just below the dc glow discharge in contact with liquid. This downflow will be effective for exchanging the chemicals at plasma-liquid interface. In this work, we investigated the characteristics of liquid flow induced by atmospheric-pressure dc glow discharge with liquid electrode in detail; the influence of voltage polarity, current amplitude, liquid conductivity, the electrode arrangement, and so on. The spatiotemporal development of liquid flow was visualized by schlieren method, and the temperature distribution was measured using temperature-sensitive liquid crystal particles dispersed in the liquid. The liquid-flow characteristics was reproduced by a fluid simulation considering a downward driving force at liquid surface from plasma. The candidate of the driving force will be the momentum transfer of charged species at the liquid surface. This work is partly supported by JSPS KAKENHI Grant Number 15H03584.