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Sample records for dowex 50w resins

  1. Distribution ratios on Dowex 50W resins of metal leached in the caron nickel recovery process

    SciTech Connect

    Reynolds, B.A.; Metsa, J.C.; Mullins, M.E.

    1980-05-01

    Pressurized ion exchange on Dowex 50W-X8 and 50W-X12 resins was investigated using elution techniques to determine distribution ratios for copper, nickel, and cobalt complexes contained in ammonium carbonate solution, a mixture which approximates the waste liquor from the Caron nickel recovery process. Results were determined for different feed concentrations, as well as for different concentrations and pH values of the ammonium carbonate eluant. Distribution ratios were compared with those previously obtained from a continuous annular chromatographic system. Separation of copper and nickel was not conclusively observed at any of the conditions examined.

  2. Preconcentration of trace multi-elements in water samples using Dowex 50W-x8 and Chelex-100 resins prior to their determination using inductively coupled plasma atomic emission spectrometry (ICP-OES)

    NASA Astrophysics Data System (ADS)

    Nomngongo, Philiswa N.; Catherine Ngila, J.; Msagati, Titus A. M.; Moodley, Brenda

    This work presents a solid phase extraction (SPE) method for simultaneous preconcentration of trace elements in water samples prior to their ICP-OES determination. Dowex 50W-x8 and Chelex-100 resins were used as SPE sorbent materials for preconcentration of trace Cd, Co, Cr, Cu, Fe, Ni, Pb and Zn. The optimum sample pH, eluent concentration and sample flow rates were found to 6, 3.0 mol L-1 and 3.0 mL min-1, respectively. In terms of multi-element preconcentration capabilities, Dowex 50W-x8 appeared to be a better sorbent. The recoveries for all the tested analytes were >95%. However, Chelex-100 showed a better performance in terms of recovery (>95%) towards Cu, Fe and Zn. Under optimized conditions using Dowex 50W-x8, the relative standard deviations for different metals were <3%. The limits of detection and limits of quantification ranged from 0.01-0.39 μg L-1 and 0.05-0.1.3 μg L-1, respectively. The accuracy of the preconcentration method was confirmed by spike recovery test and the analysis of certified reference materials. The SPE method was applied for preconcentration of the analyte ions in tap water, bottled water and wastewater samples.

  3. LAB STUDY ON REGENERATION OF SPENT DOWEX 21K 16-20 MESH ION EXCHANGE RESIN

    SciTech Connect

    DUNCAN, J.B.

    2007-01-24

    Currently the effort to remove chromate from groundwater in the 100K and 100H Areas uses DOWEX 21K 16-20. This report addresses the procedure and results of a laboratory study for regeneration of the spent resin by sodium hydroxide, sulfuric acid, or sodium sulfate to determine if onsite regeneration by the Effluent Treatment Facility is a feasible option.

  4. Determination of equilibrium constants of alkaline earth metal ion chelates with Dowex A-1 chelating resin.

    PubMed

    Harju, L; Krook, T

    1995-03-01

    A complexation chemistry model is applied to chelating ion-exchange systems and a method is presented for the determination of equilibrium constants for metal ion chelates with these resins. Protonation constants for the iminodiacetic based chelating resin Dowex A-1 were determined from potentiometric pH-data. Equilibrium constants were determined for 1:1 beryllium, magnesium, calcium, strontium and barium chelates with the resin in a wide pH range by measuring the concentrations of respective metal ions in the aqueous phase with direct current plasma atomic emission spectrometry (DCP-AES). A batch technique was used for the equilibrium experiments. At pH below 7 protonated 1:1 species were also found to be formed with the resin. From the obtained equilibrium constants, theoretical distribution coefficients were calculated as function of pH for respective metal ion resin system. PMID:18966248

  5. Determination of γ-Aminobutyric Acid (GABA) in Rambutan Fruit cv. Rongrian by HPLC-ELSD and Separation of GABA from Rambutan Fruit Using Dowex 50W-X8 Column.

    PubMed

    Meeploy, Maneerat; Deewatthanawong, Rujira

    2016-03-01

    A high-performance liquid chromatography method coupled with an evaporative light scattering detector (ELSD) was validated for the determination of γ-aminobutyric acid (GABA) in rambutan fruit without any sample pretreatment or derivatization. In the concentration range of 0.05-1.0 mg/mL GABA, the ELSD response was linear with a correlation coefficient (r) >0.999. Limit of detection and limit of quantitation were found to be 0.7 and 2.0 µg/mL, respectively. The method enabled the complete separation of GABA in the aqueous extract of rambutan flesh from the impurity peaks at 45.7 min. The recoveries of sample added GABA were obtained in the range of 92.0-99.3%. Intraday and interday relative standard deviations were <5.3%. Repeatability of the extraction process showed the acceptable precision. From the analysis of GABA content in rambutan flesh, 0.71 ± 0.23 mg of GABA was found in 1 g fresh weight. The recovery of GABA after passing through the Dowex 50W-X8 column was 96.65%. The analytical methodology could be potentially applied to the detection and quantification of GABA in other fruits and complex matrices when a sufficient quantity is available. PMID:26590236

  6. Chromium speciation by solid phase extraction on Dowex M 4195 chelating resin and determination by atomic absorption spectrometry.

    PubMed

    Saygi, Kadriye Ozlem; Tuzen, Mustafa; Soylak, Mustafa; Elci, Latif

    2008-05-30

    A solid phase extraction procedure has been established for chromium speciation in natural water samples prior to determination by atomic absorption spectrometry. The procedure is based on the solid phase extraction of the Cr(VI)- Dowex M 4195 chelating resin. After oxidation of Cr(III) to Cr(VI) by using H2O2, the presented method was applied to the determination of the total chromium. The level of Cr(III) is calculated by difference of total chromium and Cr(VI) levels. The procedure was optimized for some analytical parameters including pH, eluent type, flow rates of sample and eluent, matrix effects, etc. The presented method was applied for the speciation of chromium in natural water samples with satisfactory results (recoveries >95%, RSDs <10%). In the determinations of chromium species, flame atomic absorption spectrometer was used. The results were checked by using NIST SRM 2711 Montana soil and GBW 07603 Bush branched and leaves. PMID:17951001

  7. Radiation effects on amberlite IRA-938 and bio-rad AG MP-50 ion exchange resins. [Gamma radiation

    SciTech Connect

    Kazanjian, A.R.; Killion, M.E.

    1982-01-15

    The radiation stability of Amberlite IRA-938, an anion exchange resin, and Bio-Rad AG MP-50, a cation exchange resin, was investigated. The resins were gamma irradiated and analyzed for exchange capacity, gas generation, thermal stability, and plutonium capacity. The radiation stabilities were comparable to those of Dowex 11 and Dowex 50W-X8, the resins presently used in Rocky Flats recovery operations.

  8. Application of response surface methodology and artificial neural network: modeling and optimization of Cr(VI) adsorption process using Dowex 1X8 anion exchange resin.

    PubMed

    Harbi, Soumaya; Guesmi, Fatma; Tabassi, Dorra; Hannachi, Chiraz; Hamrouni, Bechir

    2016-01-01

    We report the adsorption efficiency of Cr(VI) on a strong anionic resin Dowex 1X8. The Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) analysis of this adsorbent were investigated. Response surface methodology was applied to evaluate the main effects and interactions among initial pH, initial Cr(VI) concentration, adsorbent dose and temperature. Analysis of variance depicted that resin dose and initial pH were the most significant factors. Desirability function (DF) showed that the maximum Cr(VI) removal of 95.96% was obtained at initial pH 5, initial Cr(VI) concentration of 100 mg/L, resin dose of 2 g and temperature of 283 K. Additionally, a simulated industrial wastewater containing 14.95 mg/L of Cr(VI) was treated successfully by Dowex 1X8 at optimum conditions. Same experimental design was employed to develop the artificial neural network. Both models gave a high correlation coefficient (RRSM(2) = 0.932, RANN(2) = 0.996). PMID:27191561

  9. Use of Cation Exchange Resins for Production of U{sub 3}O{sub 8} Suitable for the Al-U{sub 3}O{sub 8} Powder Metallurgy Process

    SciTech Connect

    Mosley, W.C.

    2001-09-17

    This report describes the production of U{sub 3}O{sub 8} powders from three types of cation exchange resins: Dowex 50W, a strong acid, sulfonate resin; AG MP-50, a macroporous form of sulfonate resin; and Bio-Rex 70, a weak acid, carboxylic resin.

  10. A simple method for classification of antibiotics using ion exchange resins added to agar plates.

    PubMed

    Yoshida, K; Kondo, F

    1994-01-01

    Using two different ion-exchange resins (Dowex 50W-X4 as cation and Dowex 1-X4 as anion) added directly to assay plates seeded with Bacillus subtilis or Micrococcus luteus, the size of the inhibitory zone produced by 36 antimicrobial agents around a disc or cup was characterized into various types, such as acidic, basic or amphoteric. An increase of the inhibition zone following addition of 15% Dowex 50W-X4 was evident in penicillins except for ampicillin and penicillin-G, and polyethers. Aminoglycosides, macrolides and colistin, lincomycin, and sulphonamides on assay medium treated with Dowex 1-X4 showed a similar effect on the inhibition zone. Tetracyclines, virginiamycin, oxolinic acid and furazoridone revealed no effects on the inhibition zone with either of the resins. These antibiotics could be divided into various groups on the basis of their chemical structure. This simple and rapid method may be useful for routine laboratory testing of residual antibiotics in meat. PMID:8152391

  11. Release profile comparison and stability of diltiazem-resin microcapsules in sustained release suspensions.

    PubMed

    Junyaprasert, Varaporn Buraphacheep; Manwiwattanakul, Greepol

    2008-03-20

    A sustained release suspension of diltiazem, a short half-life calcium channel blocker, was developed to reduce frequency of drug administration, ease of dose adjustment and improve patient compliance. In this study, the sustained release of diltiazem was obtained by complexing the drug with Dowex 50W x 4 and Dowex 50W x 8, strong cationic exchange resins with 4% and 8% degree of cross-linking, respectively. The diltiazem-Dowex 50W x 4 complexes provided the highest drug release and were subsequently used to prepare the microcapsules by emulsion-solvent evaporation method, using 0.75-5.00% cellulose acetate butyrate (CAB) in methylene chloride as a coating solution. As the concentration of CAB increased, the size of microcapsule increased and the drug release from the microcapsule was retarded. From release profile comparison using f(1) and f(2) factors, it was found that the microcapsules coated with 1.75% CAB provided a release profile equivalent to the commercial product of diltiazem sustained release capsule, Herbesser 90SR. Furthermore, sustained release suspensions of the diltiazem microcapsules were formulated with the use of 0.8% sodium carboxymethylcellulose or 0.4% xanthan gum as a suspending agent. The suspension of 0.4% xanthan gum showed superior in physical appearance after 120-day storage at 30 and 45 degrees C. In addition, all sustained release suspensions possessed good stability with low drug leaching and their release profiles were unchanged when compared with the dried microcapsules for 120 days at 30 and 45 degrees C. PMID:18061381

  12. Uranium Adsorption on Ion-Exchange Resins - Batch Testing

    SciTech Connect

    Mattigod, Shas V.; Golovich, Elizabeth C.; Wellman, Dawn M.; Cordova, Elsa A.; Smith, Ronald M.

    2010-12-01

    The uranium adsorption performance of five resins (Dowex 1, Dowex 21K 16-30 [fresh], Dowex 21K 16-30 [regenerated], Purofine PFA600/4740, and ResinTech SIR-1200) were tested using unspiked, nitrate-spiked, and nitrate-spiked/pH adjusted source water from well 299-W19-36. These batch tests were conducted in support of a resin selection process in which the best resin to use for uranium treatment in the 200-West Area groundwater pump-and-treat system will be identified. The results from these tests are as follows: • The data from the high-nitrate (1331 mg/L) tests indicated that Dowex 1, Dowex 21K 16-30 (fresh), Purofine PFA600/4740, and ResinTech SIR-1200 all adsorbed uranium similarly well with Kd values ranging from ~15,000 to 95,000 ml/g. All four resins would be considered suitable for use in the treatment system based on uranium adsorption characteristics. • Lowering the pH of the high nitrate test conditions from 8.2 to 7.5 did not significantly change the uranium adsorption isotherms for the four tested resins. The Kd values for these four resins under high nitrate (1338 mg/L), lower pH (7.5) ranged from ~15,000 to 80,000 ml/g. • Higher nitrate concentrations greatly reduced the uranium adsorption on all four resins. Tests conducted with unspiked (no amendments; nitrate at 337 mg/L and pH at 8.2) source water yielded Kd values for Dowex 1, Dowex 21K 16-30 (fresh), Purofine PFA600/4740, and ResinTech SIR-1200 resins ranging from ~800,000 to >3,000,000 ml/g. These values are about two orders of magnitude higher than the Kd values noted from tests conducted using amended source water. • Compared to the fresh resin, the regenerated Dowex 21K 16-30 resin exhibited significantly lower uranium-adsorption performance under all test conditions. The calculated Kd values for the regenerated resin were typically an order of magnitude lower than the values calculated for the fresh resin. • Additional testing using laboratory columns is recommended to better

  13. Assessment of cadmium in aquatic sediment using dialysis samplers with ion-exchange-resin collection

    SciTech Connect

    Shi, B.; Allen, H.E.; Desnoyers, C.

    1998-05-01

    Simultaneously extracted metals (SEM) and acid volatile sulfide (AVS) show the potential for toxicity on the basis of their ratio. Accordingly, the authors spiked cadmium in a range for which Cd/AVS ratios were from 0.2 to 10 in the sediment with its weight about 8 kg in each batch. Dialysis samplers with a cation ion-exchange resin (Dowex 50W-X4) collection were used in a laboratory for the determination of free cadmium concentrations in pore water of the collected sediment. When equilibrium was reached among cadmium in pore water, sediment, and ion-exchange resin, cadmium exchanged onto resin phase was regenerated with 1 N hydrochloric acid (OPTIMA grade) and determined using an atomic absorption spectrophotometer (Zeeman 5000) with a graphite furnace accessory. Cadmium determined using the dialysis sampler is considered as free cadmium which is related to the metal bioavailability toward aquatic biota. The developed methodology provides a new technique for assessment of free metal in aquatic sediment systems.

  14. Preparation of curium-americium oxide microspheres by resin-bead loading

    SciTech Connect

    Chattin, F.R.; Benker, D.E.; Lloyd, M.H.; Orr, P.B.; Ross, R.G.; Wiggins, J.T.

    1980-01-01

    Resin-bead loading and calcination techniques have been used to produce all curium and americium oxide feed material (about 2.2 kg) for HFIR targets since 1971. The process based on Dowex 50W resin has progressed from a series of test runs, through special production runs, into routine production in permanent equipment beginning in 1975. Key attributes of this process are its reliability, high yields, and ease of operation. The process is suited for remote operation in hot cells. Yields approaching 95% are routinely obtained and only one unacceptable product has been generated during routine production operations. There have been no problems in fabricating targets from this oxide or in the subsequent irradiation of these targets. The present scale of production of 150 to 250 g/y supplies the present need and is comparable with the level of other chemical process operations at TRU. Since the annual production is accomplished in two 8 to 12 day periods, there has been no reason to consider further scale-up. However, the rate of production could easily be doubled by simply adding a second set of calcination equipment.

  15. Sodium Guidestar Radiometry Results from the SOR's 50W Fasor

    NASA Astrophysics Data System (ADS)

    Drummond, J.; Telle, J.; Denman, C.; Hillman, P.; Moore, G.; Novotny, S.; Fugate, R.; Eichoff, M.

    Having upgraded the 20W, 589nm fasor (frequency-addition source of optical radiation) reported at the last AMOS conference to 50W, we have since produced a sodium laser guidestar (LGS) with a V1 magnitude of 5.1 for 30W of fasor power in November 2005, when the annual peak in mesospheric sodium density occurs. This corresponds to a return flux at the top of the telescope of 7000 photons/s/cm2 through one airmass. Late in May 2006, however, a return of only 1340 ph/s/cm2 (V1=6.7) for 30 W of fasor power was obtained at the annual minimum in sodium column density. Earlier in the month, with 49 W of fasor power, the LGS was only as bright as V1=6.3 because of the minimum in column density. By measuring the LGS return flux in circular polarization from various altitudes and azimuths, we have detected the presence of the Earth's magnetic field, for the first time ever, as an enhancement in flux from the direction where the field lines are pointing at the SOR. We then give a formulation to predict the brightness of the LGS as a function of direction and time of year. The fasor, itself, is continuously tunable to as fine as 60 femtometers (6x10-6 Angstroms) across the entire sodium D2 line (FWHM ~3 GHz) and is capable of pumping either the D2a or D2b feature with linear or circular polarization. Spectral scans will be shown. While saturation is now being seen for linear polarization, we have seen little, if any, saturation for circular polarization at higher laser powers, and circular produces more than twice the return of linear because of optical pumping. We have succeeded in closing the adaptive optics loop on this very bright LGS, resolving a 0.14 arcsec binary star in June 2006.

  16. Phosphate Adsorption from Membrane Bioreactor Effluent Using Dowex 21K XLT and Recovery as Struvite and Hydroxyapatite.

    PubMed

    Nur, Tanjina; Loganathan, Paripurnanda; Kandasamy, Jaya; Vigneswaran, Saravanamuthu

    2016-03-01

    Discharging phosphate through wastewaters into waterways poses a danger to the natural environment due to the serious risks of eutrophication and health of aquatic organisms. However, this phosphate, if economically recovered, can partly overcome the anticipated future scarcity of phosphorus (P) resulting from exhaustion of natural phosphate rock reserves. An experiment was conducted to determine the efficiency of removing phosphate from a membrane bioreactor effluent (pH 7.0-7.5, 20, 35 mg phosphate/L) produced in a water reclamation plant by adsorption onto Dowex 21K XLT ion exchange resin and recover the phosphate as fertilisers. The data satisfactorily fitted to Langmuir adsorption isotherm with a maximum adsorption capacity of 38.6 mg · P/g. The adsorbed phosphate was quantitatively desorbed by leaching the column with 0.1 M NaCl solution. The desorbed phosphate was recovered as struvite when ammonium and magnesium were added at the molar ratio of phosphate, ammonium and magnesium of 1:1:1 at pH 9.5. Phosphate was also recovered from the desorbed solution as hydroxyapatite precipitate by adding calcium hydroxide to the solution at a phosphate to calcium molar ratio of 1:2 at pH 7.0. The P contents of struvite and hydroxyapatite produced were close to those of the respective commercial phosphate fertilisers. PMID:26950136

  17. Phosphate Adsorption from Membrane Bioreactor Effluent Using Dowex 21K XLT and Recovery as Struvite and Hydroxyapatite

    PubMed Central

    Nur, Tanjina; Loganathan, Paripurnanda; Kandasamy, Jaya; Vigneswaran, Saravanamuthu

    2016-01-01

    Discharging phosphate through wastewaters into waterways poses a danger to the natural environment due to the serious risks of eutrophication and health of aquatic organisms. However, this phosphate, if economically recovered, can partly overcome the anticipated future scarcity of phosphorus (P) resulting from exhaustion of natural phosphate rock reserves. An experiment was conducted to determine the efficiency of removing phosphate from a membrane bioreactor effluent (pH 7.0–7.5, 20, 35 mg phosphate/L) produced in a water reclamation plant by adsorption onto Dowex 21K XLT ion exchange resin and recover the phosphate as fertilisers. The data satisfactorily fitted to Langmuir adsorption isotherm with a maximum adsorption capacity of 38.6 mg·P/g. The adsorbed phosphate was quantitatively desorbed by leaching the column with 0.1 M NaCl solution. The desorbed phosphate was recovered as struvite when ammonium and magnesium were added at the molar ratio of phosphate, ammonium and magnesium of 1:1:1 at pH 9.5. Phosphate was also recovered from the desorbed solution as hydroxyapatite precipitate by adding calcium hydroxide to the solution at a phosphate to calcium molar ratio of 1:2 at pH 7.0. The P contents of struvite and hydroxyapatite produced were close to those of the respective commercial phosphate fertilisers. PMID:26950136

  18. Investigation of an anion exchange resin for cleanup of a coolant used to machine nuclear materials

    SciTech Connect

    Hinton, E.R. Jr.; Tucker, H.L.; Asbury, W.L.

    1986-01-01

    This article describes the interaction of Dowex SBR-P, which is a strongly basic anion exchange resin, with ions found in a used machining coolant. The coolant is used in machining enriched uranium and contains uranium, chloride, nitrite, borate ions, water, and propylene glycol.

  19. 1016nm all fiber picosecond MOPA laser with 50W output.

    PubMed

    Qi, Xue; Chen, Sheng-Ping; Sun, Hai-Yue; Yang, Bing-Ke; Hou, Jing

    2016-07-25

    This paper presents an all fiber high power picosecond laser at 1016 nm in master oscillator power amplifier (MOPA) configuration. A direct amplification of this seed source encounters obvious gain competition with amplified spontaneous emission (ASE) at ~1030 nm, leading to a seriously reduced amplification efficiency. To suppress the ASE and improve the amplification efficiency, we experimentally investigate the influence of the gain fiber length and the residual ASE on the perforemance of the 1016 nm amplifier. The optimized 1016 nm MOPA laser exhibits an average power of 50 W and an optical conversion efficiency of 53%. PMID:27464139

  20. An air-cooled pulse tube cryocooler with 50 W cooling capacity at 77 K

    NASA Astrophysics Data System (ADS)

    Hu, Jianying; Wang, Xiaotao; Zhu, Jian; Chen, Shuai; Luo, Ercang; Li, Haibin

    2014-01-01

    A pulse tube cryocooler with 50 W cooling capacity at 77 K is developed to cool superconducting devices mounted on automobiles. The envisioned cryocooler weight is less than 40 kg, and the input electric power is less than 1 kW. To achieve these requirements, the working frequency is increased to 75 Hz, and the dual-opposed pistons use gas bearings to reduce compressor weight and volume. The heat from the main heat exchanger is rejected by forced convective air instead of water. The compressor and the cold finger are carefully matched to improve the efficiency. The details of these will be presented in this paper. After some adjustment, a no load temperature for the pulse tube cryocooler of 40 K was achieved with 1 kW input electric power in surroundings at 298 K. At 77 K, the cooling capacity is 50 W. If the main heat exchanger is cooled by water at 293 K, the cooling capacity increases to 64 W, corresponding to a relative Carnot efficiency of 18%.

  1. Development of Trouble Diagnosis Technology of 50W Grade Small Wind Turbine Generator

    NASA Astrophysics Data System (ADS)

    Takaoka, Masashige; Inohata, Kazuki; Miyake, Takuma; Tashima, Daisuke; Otsubo, Masahisa; Bouno, Toshio

    Establishment of an early trouble diagnosis system is demanded to prevent damage of wind turbine generator. Therefore, AE signal occurring by the damage of a wind blade was detected with the AE sensor which installed to the body of wind turbine generator and a pole. In this study, length of a blade of a small wind turbine generator was changed as simulated trouble in the constant wind velocity. The AE signal which occurred at this time was measured with an AE sensor. The signal was processed by FFT analysis, and a change of spectrum strength was examined. Then, trouble diagnosis technology of 50W grade small wind turbine generator was developed. As the results, a method to count the number of times more than threshold of AE signals was suggested by a wave pattern of an AE signal. It was understood that the number of the count was decided as standard to judge normality or abnormality of 50W grade small wind turbine generator.

  2. Evaluation of Selective Ion Exchange Resins for Removal of Mercury from the H-Area Water Treatment Unit

    SciTech Connect

    Serkiz, S.M.

    2000-09-05

    This study investigated the ability of seven ion exchange (IX) resins, some of which were mercury specific, to remove mercury in H-Area WTU waters from three sources (Reverse Osmosis (RO) Feed, RO Permeate from Train A, and a mercury ''hot spot'' extraction well HEX 18). Seven ion exchange resins, including ResinTech CG8 and Dowex 21K (the cation and anion exchange resins currently used at the H-Area WTU) were screened against five alternative ion exchange materials plus an experimental blank. Mercury decontamination factors (DFs), mercury breakthrough, and post-test contaminant concentrations of IX resins were determined for each IX material tested.

  3. InGaN power laser chips in a novel 50W multi-die package

    NASA Astrophysics Data System (ADS)

    Loeffler, Andreas; Eichler, Christoph; Mueller, Jens; Gerhard, Sven; Stojetz, Bernhard; Tautz, Soenke; Vierheilig, Clemens; Ristic, Jelena; Avramescu, Adrian; Horn, Markus; Hager, Thomas; Walter, Christoph; Dobbertin, Thomas; Koenig, Harald; Strauss, Uwe

    2015-03-01

    In this paper we report recent developments on high power blue laser chips. Reduction of internal losses as well as optimized thermal management had been essential to increase optical output power. R and D samples with average performance of 3W optical output at junction temperatures of 130°C are demonstrated. The chips are suitable for use in a novel multi chip housing: For the first time up to 20 blue laser chips have been packaged into one compact housing resulting in the first InGaN laser device with optical output > 50W. The highly integrated package offers a unique small size. The outer dimensions of the package are 25.5mm x 35mm with an emitting surface of 16mm x 16.5mm. Therefore the complexity of optical alignment is dramatically reduced and only a single sheet multi lens array is required for beam collimation. Besides the unique technical performance the multi-die package offers significantly lower assembly costs because of the reduced complexity and assembly time. The butterfly package contains 4 bars with up to 5 multimode laser chips in series connection on each bar operating at 2.3A. The typical module wavelength is 450nm +/- 10nm. At a case temperature of 50°C the R and D samples achieve efficiencies of typ. 30% and an optical output power of 50W corresponding to an electrical power consumption of ~165W. This new technology can be used for high performance light engines of high brightness projectors.

  4. Performance of selected anion exchange resins for the treatment of a high DOC content surface water.

    PubMed

    Humbert, Hugues; Gallard, Hervé; Suty, Hervé; Croué, Jean-Philippe

    2005-05-01

    The objective of this study was first to compare the performance of four strong anion exchange resins (AERs) (MIEX from Orica Pty Ltd, DOWEX-11 and DOWEX-MSA from DOW chemical and IRA-938 from Rohm and Haas) for their application in drinking water treatment (natural organic matter (NOM), mineral anions (nitrate, sulfate and bromide) and pesticide removal) using bench-scale experimental procedures on a high DOC content surface water. The efficiency of MIEX for NOM and mineral anions removal was furthermore evaluated using bench-scale dose-response experiments on raw, clarified and post-ozonated waters. NOM removal was assessed using the measurement of dissolved organic carbon (DOC), UV absorbance at 254 nm (UV254) and the use of high-performance size exclusion chromatography with UV (HPSEC/UV) and fluorescence detection (HPSEC/FLUO). The MIEX and IRA938 anionic resins exhibit a faster removal of NOM and mineral anions compared to the DOWEX11 and MSA AERs. All the resins were found to be very effective with similar performances after 30 to 45 min of contact time. As expected, only limited sorption of atrazine and isoproturon (C0=1 microg/L) occurred with MIEX, DOWEX11 and MSA AERs. MIEX resin proved to be very efficient in eliminating NOM of high-molecular weight but also a large part of the smallest UV absorbing organic compounds which were refractory to coagulation/flocculation treatment. Remaining DOC levels after 30 min of contact with MIEX were found similar in raw water, clarified water and even post-ozonated water implying no DOC benefit can be gained by employing conventional treatment prior to MIEX treatment. Removal of bromide (initial concentration 110 microg/L) was also observed and ranged from 30% to 65% for resin dose increasing from 2 to 8 mL/L. T PMID:15899268

  5. Comparison between 50 W tapered laser arrays and tapered single emitters

    NASA Astrophysics Data System (ADS)

    Scholz, Christian; Boucke, Konstantin; Poprawe, Reinhart; Keleman, Marc T.; Weber, Jürgen; Mikulla, Michael; Weimann, Günter

    2006-02-01

    During the last few years high power diode laser arrays have become well established for direct material processing due to their high efficiency of more than 50%. But standard broad-area waveguide designs are susceptible to modal instabilities and filamentations resulting in low beam qualities. The beam quality increases by more than a factor of four by using tapered laser arrays, but so far they suffer from lower efficiencies. Therefore tapered lasers are mainly used today as single emitters in external resonator configurations. With increased output power and lifetime, they will be much more attractive for material processing and for pumping of fiber amplifiers. High efficiency tapered mini bars emitting at a wavelength of 980 nm are developed, and in order to qualify the bars, the characteristics of single emitters and mini bars from the same wafer have been compared. The mini bars have a width of 6 mm with 12 emitters. The ridge waveguide tapered lasers consist of a 500 μm long ridge and a 2000 μm long tapered section. The results show very similar behavior of the electro-optical characteristics and the beam quality for single emitters and bars. Due to different junction temperatures, different slope efficiencies were measured: 0.8 W/A for passively cooled mini bars and 1.0 W/A for actively cooled mini-bars and single emitters. The threshold current of 0.7 A per emitter is the same for single emitters and emitter arrays. Output powers of more than 50 W in continuous wave mode for a mini bar with standard packaging demonstrates the increased power of tapered laser bars.

  6. The effects of ionizing radiation on Reillex trademark HPQ, a new macroporous polyvinylpyridine resin, and on four conventional polystyrene anion exchange resins

    SciTech Connect

    Marsh, S.F.

    1990-11-01

    This study compares the effects of ionizing radiation on Reillex{trademark} HPQ, a recently available macroporous copolymer of 1-methyl-4-vinylpyridine/divinylbenzene, and on four conventional strong-base polystyrene anion exchange resins. The polystyrene resins investigated included one gel type, Dowex{trademark} 1 {times} 4, and three macroporous resins: Dow{trademark} MSA-1, Amberlite{trademark} IRA-900, and Lewatit{trademark} MP-500-FK. Each resin, in 7 M nitric acid, was subjected to seven different levels of {sup 60}Co gamma radiation ranging from 100 to 1000 megarads. Irradiated resins were measured for changes in dry weight, wet volume, chloride and Pu(IV) exchange capacities, and thermal stability. In separate experiments, each resin was subjected to approximately 340 megarads of in situ alpha particles from sorbed plutonium. Resin damage from alpha particles was less than half that caused by gamma rays, which may be a consequence of different production rates of radiolytic nitrite and nitro radicals in the two systems. Reillex{trademark} HPQ resin provided the greatest radiation stability, whereas Lewatit{trademark} MP-500-FK was the least stable of the resins tested. Thermogravimetric analyses of dry, nitrate-form resin revealed that dry Reillex{trademark} HPQ resin offered the best thermal stability for absorbed gamma doses to 370 megarads, but the worst thermal stability after exposures of 550 megarads or more. 25 refs., 11 figs., 13 tabs.

  7. Evaluating ion exchange resin efficiency and oxidative capacity for the separation of uranium(IV) and uranium(VI)

    PubMed Central

    2013-01-01

    Background Previously described methods to separate dissolved U(IV) from dissolved U(VI) under acidic anoxic conditions prior to laboratory analysis were ineffective with materials currently available commercially. Three strong anion exchange resins were examined for their efficiency in separating, recovering, and preserving both redox states during separation. Results Under oxic conditions, recovery of U(VI) from three exchange resins (Bio-Rad AG® 1x8 Poly-Prep® prefilled columns, Bio-Rad AG® 1x8 powder, and Dowex® 1x8 powder) ranged from 72% to 100% depending on the dosed mass, eluent volume, and resin selected. Dowex® 1x8 resin was the only resin found to provide 100% recovery of U(VI) with fewer than 5 bed volumes of eluent. Under anoxic conditions, all three resins oxidized U(IV) in aqueous solutions with relatively low U(IV) concentrations (<3x10-6 M). Resin-induced oxidation was observed visually using a leuco dye, safranin-o. Oxidants associated with the resin were irreversibly reduced by the addition of Ti(III). After anoxic resin pre-treatment, a series of U(IV)/U(VI) mixtures at micro-molar levels were prepared and separated using the Dowex® 1x8 resin with 100% recovery of both U(IV) and U(VI) with no resin-induced changes in oxidation state. Conclusions Currently available anion exchange resins with apparently identical physical properties were found to have significantly different recoveries for hexavalent uranium at micro-molar concentrations. A novel qualitative technique was developed to visually assess oxidative capacities of anion exchange resins under acidic anoxic conditions. A protocol was developed for pre-treatment and use of currently available anion exchange resins to achieve quantitative separation of U(IV) and U(VI) in aqueous solutions with low U(IV) concentrations. This method can be applied to future work to quantitatively assess dissolved U(IV) and U(VI) concentrations in both laboratory and field samples. PMID:23363052

  8. Uranium removal from contaminated groundwater by synthetic resins.

    PubMed

    Phillips, D H; Gu, B; Watson, D B; Parmele, C S

    2008-01-01

    Synthetic resins are shown to be effective in removing uranium from contaminated groundwater. Batch and field column tests showed that strong-base anion-exchange resins were more effective in removing uranium from both near-neutral-pH (6.5)- and high-pH (8)-low-nitrate-containing groundwaters, than metal-chelating resins, which removed more uranium from acidic-pH (5)-high-nitrate-containing groundwater from the Oak Ridge Reservation (ORR) Y-12 S-3 Ponds area in Tennessee, USA. Dowex 1-X8 and Purolite A-520E anion-exchange resins removed more uranium from high-pH (8)-low-nitrate-containing synthetic groundwater in batch tests than metal-chelating resins. The Dowex 21K anion-exchange resin achieved a cumulative loading capacity of 49.8 mg g(-1) before breakthrough in a field column test using near-neutral-pH (6.5)-low-nitrate-containing groundwater. However, in an acidic-pH (5)-high-nitrate-containing groundwater, metal-chelating resins Diphonix and Chelex-100 removed more uranium than anion-exchange resins. In 15 m L of acidic-pH (5)-high-nitrate-containing groundwater spiked with 20 mg L(-1) uranium, the uranium concentrations ranged from 0.95 mg L(-1) at 1-h equilibrium to 0.08 mg L(-1) at 24-h equilibrium for Diphonix and 0.17 mg L(-1) at 1-h equilibrium to 0.03 mg L(-1) at 24-h equilibrium for Chelex-100. Chelex-100 removed more uranium in the first 10 min in the 100mL of acidic-(pH 5)-high-nitrate-containing groundwater ( approximately 5 mg L(-1) uranium); however, after 10 min, Diphonix equaled or out-performed Chelex-100. This study presents an improved understanding of the selectivity and sorption kenetics of a range of ion-exchange resins that remove uranium from both low- and high-nitrate-containing groundwaters with varying pHs. PMID:17697694

  9. Uranium Removal from Contaminated Groundwater by Synthetic Resins

    SciTech Connect

    Phillips, Debra H.; Gu, Baohua; Watson, David B; Parmele, C. S.

    2008-01-01

    Synthetic resins are shown to be effective in removing uranium from contaminated groundwater. Batch and field column tests showed that strong-base anion-exchange resins were more effective in removing uranium from both near-neutral-pH (6.5)- and high-pH (8)-low-nitrate-containing ground waters, than metal-chelating resins, which removed more uranium from acidic-pH (5)-high-nitrate-containing groundwater from the Oak Ridge Reservation (ORR) Y-12 S-3 Ponds area in Tennessee, USA. Dowex 1-X8 and Purolite A-520E anion-exchange resins removed more uranium from high-pH (8)-low-nitrate-containing synthetic groundwater in batch tests than metal-chelating resins. The Dowex{trademark} 21K anion-exchange resin achieved a cumulative loading capacity of 49.8 mg g{sup -1} before breakthrough in a field column test using near-neutral-pH (6.5)-low-nitrate-containing groundwater. However, in an acidic-pH (5)-high-nitrate-containing groundwater, metal-chelating resins Diphonix and Chelex-100 removed more uranium than anion-exchange resins. In 15 mL of acidic-pH (5)-high-nitrate-containing groundwater spiked with 20 mg L{sup -1} uranium, the uranium concentrations ranged from 0.95 mg L{sup -1} at 1-h equilibrium to 0.08 mg L{sup -1} at 24-h equilibrium for Diphonix and 0.17 mg L{sup -1} at 1-h equilibrium to 0.03 mg L{sup -1} at 24-h equilibrium for Chelex-100. Chelex-100 removed more uranium in the first 10 min in the 100 mL of acidic-(pH 5)-high-nitrate-containing groundwater (5 mg L{sup -1} uranium); however, after 10 min, Diphonix equaled or out-performed Chelex-100. This study presents an improved understanding of the selectivity and sorption kinetics of a range of ion-exchange resins that remove uranium from both low- and high-nitrate-containing groundwaters with varying pHs.

  10. Evaluation and application of anion exchange resins to measure groundwater uranium flux at a former uranium mill site.

    PubMed

    Stucker, Valerie; Ranville, James; Newman, Mark; Peacock, Aaron; Cho, Jaehyun; Hatfield, Kirk

    2011-10-15

    Laboratory tests and a field validation experiment were performed to evaluate anion exchange resins for uranium sorption and desorption in order to develop a uranium passive flux meter (PFM). The mass of uranium sorbed to the resin and corresponding masses of alcohol tracers eluted over the duration of groundwater installation are then used to determine the groundwater and uranium contaminant fluxes. Laboratory based batch experiments were performed using Purolite A500, Dowex 21K and 21K XLT, Lewatit S6328 A resins and silver impregnated activated carbon to examine uranium sorption and extraction for each material. The Dowex resins had the highest uranium sorption, followed by Lewatit, Purolite and the activated carbon. Recoveries from all ion exchange resins were in the range of 94-99% for aqueous uranium in the environmentally relevant concentration range studied (0.01-200 ppb). Due to the lower price and well-characterized tracer capacity, Lewatit S6328 A was used for field-testing of PFMs at the DOE UMTRA site in Rifle, CO. The effect on the flux measurements of extractant (nitric acid)/resin ratio, and uranium loading were investigated. Higher cumulative uranium fluxes (as seen with concentrations>1 ug U/gram resin) yielded more homogeneous resin samples versus lower cumulative fluxes (<1 ug U/gram resin), which caused the PFM to have areas of localized concentration of uranium. Resin homogenization and larger volume extractions yield reproducible results for all levels of uranium fluxes. Although PFM design can be improved to measure flux and groundwater flow direction, the current methodology can be applied to uranium transport studies. PMID:21798572

  11. Cement waste-form development for ion-exchange resins at the Rocky Flats Plant

    SciTech Connect

    Veazey, G.W.; Ames, R.L.

    1997-03-01

    This report describes the development of a cement waste form to stabilize ion-exchange resins at Rocky Flats Environmental Technology Site (RFETS). These resins have an elevated potential for ignition due to inadequate wetness and contact with nitrates. The work focused on the preparation and performance evaluation of several Portland cement/resin formulations. The performance standards were chosen to address Waste Isolation Pilot Plant and Environmental Protection Agency Resource Conservation and Recovery Act requirements, compatibility with Rocky Flats equipment, and throughput efficiency. The work was performed with surrogate gel-type Dowex cation- and anion-exchange resins chosen to be representative of the resin inventory at RFETS. Work was initiated with nonactinide resins to establish formulation ranges that would meet performance standards. Results were then verified and refined with actinide-containing resins. The final recommended formulation that passed all performance standards was determined to be a cement/water/resin (C/W/R) wt % ratio of 63/27/10 at a pH of 9 to 12. The recommendations include the acceptable compositional ranges for each component of the C/W/R ratio. Also included in this report are a recommended procedure, an equipment list, and observations/suggestions for implementation at RFETS. In addition, information is included that explains why denitration of the resin is unnecessary for stabilizing its ignitability potential.

  12. Determination of Pb(II) by Photoacoustic Spectroscopy with a Solid-Phase Spectrophotometry Approach Using 2-(2-Thiazolylazo)--cresol (TAC) Coated on Resin

    NASA Astrophysics Data System (ADS)

    Saavedra, R.; Gómez, R.; Soto, C.; Aguayo, D.; Candia, C.; Yañez, J.; Zuñiga, V.

    2013-09-01

    In this study, preliminary results obtained for Pb(II) determination by photoacoustic spectroscopy are introduced. It is based on an amplitude measurement of a photoacoustic signal obtained from a Pb(II) complex formation with2-(2-thiazolylazo)- p-cresol (TAC) retained in an anionic resin such as Dowex 1X8. The Pb(II)-TAC complex spectrum reveals an absorption band, which is assigned to a Pb(II)-TAC complex retained on the resin. The peak height of this band is proportional to the Pb(II) concentration, and it can be used to obtain quantitative information of the metal content.

  13. Decomposition of Rare Earth Loaded Resin Particles

    SciTech Connect

    Voit, Stewart L; Rawn, Claudia J

    2010-09-01

    The Fuel Cycle R and D (FCR and D) program within the Department of Energy Office of Nuclear Energy (DOE-NE) is evaluating nuclear fuel cycle options, including once-through, modified open, and fully closed cycles. Each of these scenarios may utilize quite different fuel management schemes and variation in fuel types may include high thermal conductivity UO{sub 2}, thoria-based, TRISO, metal, advanced ceramic (nitride, carbide, composite, etc.), and minor actinide (MA) bearing fuels and targets. Researchers from the US, Europe, and japan are investigating methods of fabricating high-specific activity spherical particles for fuel and target applications. The capital, operating, and maintenance costs of such a fuel fabrication facility can be significant, thus fuel synthesis and fabrication processes that minimize waste and process losses, and require less footprint are desired. Investigations have been performed at the Institute for Transuranium Elements (ITU) and the French Atomic Energy Commission (CEA) studying the impact of americium and curium on the fuel fabrication process. proof of concept was demonstrated for fabrication of MA-bearing spherical particles, however additional development will be needed for engineering scale-up. Researchers at the Paul Scherer Institute (PSI) and the Japan Atomic Energy Association (JAEA) have collaborated on research with ceramic-metallic (CERMET) fuels using spherical particles as the ceramic component dispersed in the metal matrix. Recent work at the CEA evaluates the burning of MA in the blanket region of sodium fast reactors. There is also interest in burning MA in Canada Deuterium Uranium (CANDU) reactors. The fabrication of uranium-MA oxide pellets for a fast reactor blanket or MA-bearing fuel for CANDU reactors may benefit from a low-loss dedicated footprint for producing MA-spherical particles. One method for producing MA-bearing spherical particles is loading the actinide metal on a cation exchange resin. The AG-50W

  14. Femtosecond pulses at 50-W average power from an Yb:YAG planar waveguide amplifier seeded by an Yb:KYW oscillator.

    PubMed

    Leburn, Christopher G; Ramírez-Corral, Cristtel Y; Thomson, Ian J; Hall, Denis R; Baker, Howard J; Reid, Derryck T

    2012-07-30

    We report the demonstration of a high-power single-side-pumped Yb:YAG planar waveguide amplifier seeded by an Yb:KYW femtosecond laser. Five passes through the amplifier yielded 700-fs pulses with average powers of 50 W at 1030 nm. A numerical simulation of the amplifier implied values for the laser transition saturation intensity, the small-signal intensity gain coefficient and the gain bandwidth of 10.0 kW cm(-2), 1.6 cm(-1), and 3.7 nm respectively, and identified gain-narrowing as the dominant pulse-shaping mechanism. PMID:23038288

  15. 50W CW visible laser source at 589nm obtained via frequency doubling of three coherently combined narrow-band Raman fibre amplifiers.

    PubMed

    Taylor, Luke R; Feng, Yan; Calia, Domenico Bonaccini

    2010-04-12

    We demonstrate the cascaded coherent collinear combination of a seed-split triplet of 1178nm high-power narrow-band (sub-1.5MHz) SBS-suppressed CW Raman fibre amplifiers via nested free-space constructive quasi-Mach-Zehnder interferometry, after analysing the combination of the first two amplifiers in detail. Near-unity combination and cascaded-combination efficiencies are obtained at all power levels up to a maximum P(1178) > 60W. Frequency doubling of this cascaded-combined output in an external resonant cavity yields P(589) > 50W with peak conversion efficiency eta(589) ~85%. We observe no significant differences between the SHG of a single, combined pair or triplet of amplifiers. Although the system represents a successful power scalability demonstrator for fibre-based Na-D(2a)-tuned mesospheric laser-guide-star systems, we emphasise its inherent wavelength versatility and consider its spectroscopic and near-diffraction-limited qualities equally well suited to other applications. PMID:20588700

  16. Collection and spectral control of high-order harmonics generated with a 50 W high-repetition rate Ytterbium femtosecond laser system

    NASA Astrophysics Data System (ADS)

    Cabasse, A.; Hazera, Ch; Quintard, L.; Cormier, E.; Petit, S.; Constant, E.

    2016-04-01

    We generate high-order harmonics with a 50 W, Yb femtosecond fiber laser system operating at 100 kHz in a tight focusing configuration. We achieve a high photon flux even with pulses longer than 500 fs. We collect the diverging extreme ultraviolet (XUV) harmonic beam in a 35 mrad wide solid angle by using a spectrometer designed to handle the high thermal load under vacuum and refocus the XUV beam onto a detector where the beam is characterised or can alternatively be used for experiments. This setup is designed for a 50 eV XUV bandwidth and offers the possibility to perform XUV-IR pump probe experiments with both temporal and spectral resolution. The high-order harmonics were generated and optimized at 100 kHz by using several gas target geometries (a gas jet and a semi-infinite gas cell) and several gases (argon, krypton, xenon) that provide XUV beams with different characteristics. After the spectrometer and for high-order harmonic generation (HHG) in xenon, we detect more than 4 × 1010 photons per second over four harmonics, that is a useful XUV power on target of 0.1 μW. This corresponds to the emission of more than 1 μW per harmonic at the source and we achieved a similar flux with both the semi-infinite cell and the jet. In addition, we observe a strong spectral selectivity when generating harmonics in a semi-infinite gas cell as few harmonics clearly dominate the neighbouring harmonics. We attribute this spectral selectivity to phase matching effects.

  17. Emission spectrographic determination of barium in sea water using a cation exchange concentration procedure

    USGS Publications Warehouse

    Szabo, B. J.; Joensuu, O.

    1967-01-01

    A concentration technique employing Dowex 50W cation exchange resin is described for the determination of barium in sea water. The separated barium is precipitated as fluoride together with calcium and strontium and measured by emission spectrographic analysis. The vertical distribution of barium in sea water has been measured in the Caribbean Sea and the Atlantic Ocean. The barium content varied between 7 and 23 ??g. per liter; in two profiles, the lowest concentrations were at a depth of about 1000 meters.

  18. A theoretical model for the separation of glucose and fructose mixtures by using a semicontinuous chromatographic refiner

    SciTech Connect

    Lee, Kwang Nam; Lee, Won Kook )

    1992-03-01

    The separation of a glucose and fructose mixture was experimentally performed by using a semicontinuous chromatographic refiner (SCCR) packed with Ca{sup 2+} ion in the form of DOWEX 50W 12X resin. The plug flow model with velocity-dependent mass transfer resistance was resistance was presented for calculating both products and on-concentrations in the SCCR unit, and the validity of the model was experimentally confirmed.

  19. Incombustible resin composition

    NASA Technical Reports Server (NTRS)

    Akima, T.

    1982-01-01

    Incombustible resin compositions composed of aromatic compounds were obtained through (1) combustion polymer material and (2) bisphenol A or halogenated bisphenol A and bisphenol A diglycidl ether or halogenated bisphenol A diglycidyl ether. The aromatic compound is an adduct of bifunctional phenols and bifunctional epoxy resins.

  20. Delayed cure bismaleimide resins

    DOEpatents

    Not Available

    1982-08-12

    Prior art polybismaleimides begin to polymerize at or just above the melting point of the monomer. This patent describes new bismaleimide resins which have an increased pot life and provide longer time periods in which the monomer remains fluid. The resins can be polymerized into molded articles with a high uniformity of properties. (DLC)

  1. A novel polar-modified post-cross-linked resin: Effect of the porogens on the structure and adsorption performance.

    PubMed

    Wang, Xiaomei; Fu, Zhenyu; Yu, Na; Huang, Jianhan

    2016-03-15

    The porogens used in the polymerization play important roles in the structure and adsorption performance for the polar-modified post-cross-linked resins. A series of novel polar-modified post-cross-linked resins were prepared using different mass percentage of toluene and 3-methyl-1-butanol as the mixed porogens. The results indicated that the resins using a higher mass percentage of toluene in the mixed porogens possessed a higher content of pendent vinyl groups, the greater Brunauer-Emmett-Teller (BET) surface area and t-plot micropore surface area. What's more, the Friedel-Crafts alkylation reaction induced a higher increment of the BET surface area and t-plot micropore surface area before and after the post-cross-linking. The resin p(GMA-co-DVB)-22-pc using 50% (w/w) of toluene and 50% (w/w) of 3-methyl-1-butanol in the mixed porogens held the largest equilibrium capacity to phenol among the four considered resins. The equilibrium data was well characterized by the Freundlich model and the isosteric enthalpy decreased dramatically with increasing of the fractional loading. The resin using a lower mass percentage of toluene in the mixed porogens required less time to reach equilibrium because of its less micropores and the minor diffusion resistance in the pores. p(GMA-co-DVB)-22-pc exhibited a dynamic saturated capacity of 55.4 mg/mL wet resin at an initial concentration of 1250 mg/L and a flow rate of 1.4 mL/min, and it could be completely regenerated by 0.001 mol/L of sodium hydroxide (w/v) and 80% of ethanol (v/v). PMID:26748064

  2. Development of resins for composites by resin transfer molding

    NASA Technical Reports Server (NTRS)

    Woo, Edmund P.; Puckett, Paul M.; Maynard, Shawn J.

    1991-01-01

    Designed to cover a wide range of resin technology and to meet the near-term and long-term needs of the aircraft industry, this research has three objectives: to produce resin transfer molding (RES) resins with improved processability, to produce prepreg systems with high toughness and service temperature, and to produce new resin systems. Progress on reaching the objectives is reported.

  3. Biocompatibility of composite resins

    PubMed Central

    Mousavinasab, Sayed Mostafa

    2011-01-01

    Dental materials that are used in dentistry should be harmless to oral tissues, so they should not contain any leachable toxic and diffusible substances that can cause some side effects. Reports about probable biologic hazards, in relation to dental resins, have increased interest to this topic in dentists. The present paper reviews the articles published about biocompatibility of resin-restorative materials specially resin composites and monomers which are mainly based on Bis-GMA and concerns about their degradation and substances which may be segregated into oral cavity. PMID:23372592

  4. Biocidal quaternary ammonium resin

    NASA Technical Reports Server (NTRS)

    Janauer, G. E.

    1983-01-01

    Activated carbon (charcoal) and polymeric resin sorbents are widely used in the filtration and treatment of drinking water, mainly to remove dissolved organic and inorganic impurities and to improve the taste. Earlier hopes that activated carbon might "disinfect' water proved to be unfounded. The feasibility of protecting against microbial infestation in charcoal and resin beds such as those to be incorporated into total water reuse systems in spacecraft was investigated. The biocidal effect of IPCD (insoluable polymeric contact disinfectants) in combination with a representative charcoal was assessed. The ion exchange resins (IPCD) were shown to adequately protect charcoal and ion exchange beds.

  5. Thermally stable laminating resins

    NASA Technical Reports Server (NTRS)

    Jones, R. J.; Vaughan, R. W.; Burns, E. A.

    1972-01-01

    Improved thermally stable laminating resins were developed based on the addition-type pyrolytic polymerization. Detailed monomer and polymer synthesis and characterization studies identified formulations which facilitate press molding processing and autoclave fabrication of glass and graphite fiber reinforced composites. A specific resin formulation, termed P10P was utilized to prepare a Courtaulds HMS reinforced simulated airfoil demonstration part by an autoclave molding process.

  6. Acetylene terminated matrix resins

    NASA Technical Reports Server (NTRS)

    Goldfarb, I. J.; Lee, Y. C.; Arnold, F. E.; Helminiak, T. E.

    1985-01-01

    The synthesis of resins with terminal acetylene groups has provided a promising technology to yield high performance structural materials. Because these resins cure through an addition reaction, no volatile by-products are produced during the processing. The cured products have high thermal stability and good properties retention after exposure to humidity. Resins with a wide variety of different chemical structures between the terminal acetylene groups are synthesized and their mechanical properties studied. The ability of the acetylene cured polymers to give good mechanical properties is demonstrated by the resins with quinoxaline structures. Processibility of these resins can be manipulated by varying the chain length between the acetylene groups or by blending in different amounts of reactive deluents. Processing conditions similar to the state-of-the-art epoxy can be attained by using backbone structures like ether-sulfone or bis-phenol-A. The wide range of mechanical properties and processing conditions attainable by this class of resins should allow them to be used in a wide variety of applications.

  7. 1-Butanol absorption in poly(styrene-divinylbenzene) ion exchange resins for catalysis.

    PubMed

    Pérez-Maciá, M A; Curcó, D; Bringué, R; Iborra, M; Rodríguez-Ropero, F; van der Vegt, N F A; Aleman, Carlos

    2015-12-21

    The swelling behaviour of poly(styrene-co-divinylbenzene), P(S-DVB), ion exchange resins in 1-butanol (BuOH) has been studied by means of atomistic classical molecular dynamics simulations (MD). The topological characteristics reported for the resin in the dry state, which exhibited complex internal loops (macropores), were considered for the starting models used to examine the swelling induced by BuOH contents ranging from 10% to 50% w/w. Experimental measurements using a laser diffraction particle size analyzer indicate that swelling causes a volume variation with respect to the dry resin of 21%. According to MD simulations, such a volume increment corresponds to a BuOH absorption of 31-32% w/w, which is in excellent agreement with the indirect experimental estimation (i.e. 31% w/w). Simulations reveal that, independently of the content of BuOH, the density of the swelled resin is higher than that of the dry resin, evidencing that the alcohol provokes important structural changes in the polymeric matrix. Thus, BuOH molecules cause a collapse of the resin macropores when the content of alcohol is ≤20% w/w. In contrast, when the concentration of BuOH is close to the experimental value (∼30% w/w), P(S-DVB) chains remain separated by pores faciliting the access of the reactants to the reaction centers. On the other hand, evaluation of both bonding and non-bonding interactions indicates that the mixing energy is the most important contribution to the absorption of BuOH into the P(S-DVB) resin. Overall, the results displayed in this work represent a starting point for the theoretical study of the catalytic conversion of BuOH into di-n-butyl ether in P(S-DVB) ion exchange resins using sophisticated electronic methods. PMID:26411792

  8. Fractionation of sulphite spent liquor for biochemical processing using ion exchange resins.

    PubMed

    Fernandes, D L A; Silva, C M; Xavier, A M R B; Evtuguin, D V

    2012-12-31

    Sulphite spent liquor (SSL) is a side product from acidic sulphite pulping of wood, which organic counterpart is composed mainly by lignosulphonates (LS) and sugars. The last are a prominent substrate for the bioprocessing although a previous purification step is necessary to eliminate microbial inhibitors. In this study a fractionation of hardwood SSL (HSSL) has been accomplished employing ion exchange resins in order to separate sugars fraction from concomitant inhibitors: LS, acetic acid, furan derivatives, phenolics, acetic acid and excess of inorganic salts. The fractionation of HSSL has been carried out using two fixed-bed ion exchangers in series (cationic+anionic). The first cation exchange column packed with Dowex 50WX2 resin was able to eliminate free cations and partially separate sugars from high molecular weight LS and furan derivatives. The second anion exchange column packed with Amberlite IRA-96 sorbed remaining LS, phenolics and acetic acid. Overall, the series arrangement under investigation has removed 99.99% of Mg(2+), 99.0% of Ca(2+), 99.6% of LS, and 100% of acetic acid, whereas the yield of recovered sugars was at least 72% of their total amount in HSSL. PMID:22465600

  9. Using resin to generate a non-invasive intestinal bile-depleted rat model was unsuccessful.

    PubMed

    Holm, René; Hesselkilde, Janne Z; Jørgensen, Erling B; Müllertz, Anette

    2012-09-29

    The purpose of this study was to evaluate if a rat model, based upon co-administration of the anion-exchanging resin, cholestyramine, could replace surgery when evaluating the importance of bile on drug absorption. Two different formulations were used for the administration of halofantrine; polyethylene glycol 400 (PEG 400) and PEG 400/polysorbate 80 (50:50, w/w%), as a positive and negative control on the dependency of bile. No significant effect of the resin was detected after evaluation of three different pre-dosing regimes, but in line with previous studies the formulation containing polysorbate 80 showed a significant increase in the absorption of halofantrine. This study therefore demonstrates that the pre-dosing of rats with Cholestyramine can not replace surgical bile duct cannulation if a formulation needs to be evaluated for its bile dependency. PMID:22732256

  10. Graphite fiber reinforced thermoplastic resins

    NASA Technical Reports Server (NTRS)

    Novak, R. C.

    1975-01-01

    Mechanical properties of neat resin samples and graphite fiber reinforced samples of thermoplastic resins were characterized with particular emphasis directed to the effects of environmental exposure (humidity, temperature and ultraviolet radiation). Tensile, flexural, interlaminar shear, creep and impact strengths were measured for polysulfone, polyarylsulfone and a state-of-the-art epoxy resin samples. In general, the thermoplastic resins exhibited environmental degradation resistance equal to or superior to the reference epoxy resin. Demonstration of the utility and quality of a graphite/thermoplastic resin system was accomplished by successfully thermoforming a simulated compressor blade and a fan exit guide vane.

  11. The effectiveness of four organic matter amendments for decreasing resin-extractable Cr(VI) in Cr(VI)-contaminated soils.

    PubMed

    Chiu, Chien-Chih; Cheng, Chia-Jung; Lin, Tzu-Huei; Juang, Kai-Wei; Lee, Dar-Yuan

    2009-01-30

    This paper compared the effectiveness of four organic materials for decreasing the amounts of soil extractable Cr(VI) in Cr(VI)-contaminated soils using the DOWEX M4195 resin-extraction method. Organic matters were added into Cr(VI)-spiked soils [500 mg Cr(VI)(kgsoil)(-1)] in the form of sugarcane dregs compost (SCDC), cattle-dung compost (CDC), soybean meal (SBM) and rice bran (RB), in the amounts of 0, 1%, and 2% by dry weight, respectively. The results indicated that adding only 1% organic matter to the studied soils could effectively decrease the amount of soil resin-extractable Cr(VI) after 12 days of incubation. The decrease of resin-extractable Cr(VI) by organic materials was mainly the result from the reduction of Cr(VI) to Cr(III) supported by the XANES spectroscopy. Among the four tested organic materials, SBM and RB had higher effectiveness in decreasing soil resin-extractable Cr(VI) than CDC and SCDC. This result may be due to the fact that SBM and RB have more dissolved organic carbon (DOC) and protein than CDC and SCDC. Therefore, it was concluded that the contents of DOC and protein are the main factors that determine the effectiveness of organic materials for decreasing the amounts of soil available Cr(VI) in Cr(VI)-contaminated soils. PMID:18524481

  12. Conductivity measures coupled with treatment with ion-exchange resin for the assessment of sodium concentration in physiological fluids: analyses on artificial solutions

    NASA Astrophysics Data System (ADS)

    Tura, A.; Sbrignadello, S.; Mambelli, E.; Ravazzani, P.; Santoro, A.; Pacini, G.

    2013-09-01

    In humans, sodium is essential for the regulation of blood volume and pressure. During hemodialysis, sodium measurement is important to preserve the patient from hypo- or hyper-natremia Usually, sodium measurement is performed through laboratory equipment which is typically expensive, and requires manual intervention. We propose a new method, based on conductivity measurement after treatment of dialysate solution through ion-exchange resin. To test this method, we performed in vitro experiments. We prepared 40 ml sodium chloride (NaCl) samples at 280, 140, 70, 35, 17.5, 8.75, 4.375 mEq/l, and some "mixed samples", i.e., with added potassium chloride (KCl) at different concentrations (4.375-17.5 mEq/l), to simulate the confounding factors in a conductivity-based sodium measurement. We measured the conductivity of all samples. Afterwards, each sample was treated for 1 min with 1 g of Dowex G-26 resin, and conductivity measured again. On average, the difference ɛ in the conductivity between mixed samples and corresponding pure NaCl samples (at the same NaCl concentration) was 20.9%. With treatment with the resin, it was 9.9%, only. We conclude that ion-exchange resin treatment coupled with conductivity measures may be a possible simple approach for continuous and automatic sodium measurement during hemodialysis.

  13. Enhancement of uranium loading on ion exchange resin from carbonate leachate by lowering pH from 8 to 6. 5

    SciTech Connect

    Otto, J.B.

    1984-06-01

    This paper discusses a laboratory study that shows the saturation ion-exchange loading of uranium from carbonate leachate can be doubled by lowering the pH of the leachate from 8 to 6.5. Small column and batch resin loading tests using Dowex 21K ion-exchange resin are described. The leachate contained 3,300 ppm chloride, 2,400 ppm carbonate, and 220 ppm U/sub 3/O/sub 8/, and had a pH of 8. Even at this rather mild salinity the saturation ion-exchange loading was found to be only about 3 to 4 lbm U/sub 3/O/sub 8//cu ft resin (48 to 64 g/dm/sup 3/) because of competition with the chloride ion for exchange sites on the anionic resin. Lowering the pH of the leachate to 6.5 by CO/sub 2/ gas addition, however, increased loading to about 8 lbm U/sub 3/O/sub 8//cu ft resin (128 g/dm/sup 3/). The pH-lowering effect worked especially well at relatively high salt concentration. The same leachate, with its chloride content increased to 12,000 ppm, loaded only 0.5 lbm U/sub 3/O/sub 8//cu ft resin (8 g/dm/sup 3/) at pH 8 but loaded 5.5 lbm U/sub 3/O/sub 8//cu ft resin (88 g/dm/sup 3/) at pH 6.5.

  14. Sodium Concentration Measurement during Hemodialysis through Ion-Exchange Resin and Conductivity Measure Approach: In Vitro Experiments

    PubMed Central

    Tura, Andrea; Sbrignadello, Stefano; Mambelli, Emanuele; Ravazzani, Paolo; Santoro, Antonio; Pacini, Giovanni

    2013-01-01

    Sodium measurement during hemodialysis treatment is important to preserve the patient from clinical events related to hypo- or hyper-natremia Usually, sodium measurement is performed through laboratory equipment which is typically expensive, and requires manual intervention. We propose a new method, based on conductivity measurement after treatment of dialysate solution through ion-exchange resin. To test this method, we performed in vitro experiments. We prepared 40 ml sodium chloride (NaCl) samples at 280, 140, 70, 35, 17.5, 8.75, 4.375 mEq/l, and some “mixed samples”, i.e., with added potassium chloride (KCl) at different concentrations (4.375-17.5 mEq/l), to simulate the confounding factors in a conductivity-based sodium measurement. We measured the conductivity of all samples. Afterwards, each sample was treated for 1 min with 1 g of Dowex G-26 resin, and conductivity was measured again. On average, the difference in the conductivity between mixed samples and corresponding pure NaCl samples (at the same NaCl concentration) was 20.9%. After treatment with the exchange resin, it was 14.7%, i.e., 42% lower. Similar experiments were performed with calcium chloride and magnesium chloride as confounding factors, with similar results. We also performed some experiments on actual dialysate solution during hemodialysis sessions in 15 patients, and found that the correlation between conductivity measures and sodium concentration improved after resin treatment (R=0.839 before treatment, R=0.924 after treatment, P<0.0001). We conclude that ion-exchange resin treatment coupled with conductivity measures may improve the measurement of sodium compared to conductivity measures alone, and may become a possible simple approach for continuous and automatic sodium measurement during hemodialysis. PMID:23844253

  15. Method for removing contaminants from plastic resin

    DOEpatents

    Bohnert, George W.; Hand, Thomas E.; DeLaurentiis, Gary M.

    2008-12-09

    A resin recycling method that produces essentially contaminant-free synthetic resin material in an environmentally safe and economical manner. The method includes receiving the resin in container form. The containers are then ground into resin particles. The particles are exposed to a solvent, the solvent contacting the resin particles and substantially removing contaminants on the resin particles. After separating the particles and the resin, a solvent removing agent is used to remove any residual solvent remaining on the resin particles after separation.

  16. Phosphonic acid based exchange resins

    DOEpatents

    Horwitz, E. Philip; Alexandratos, Spiro D.; Gatrone, Ralph C.; Chiarizia, Ronato

    1995-01-01

    An ion exchange resin for extracting metal ions from a liquid waste stream. An ion exchange resin is prepared by copolymerizing a vinylidene diphosphonic acid with styrene, acrylonitrile and divinylbenzene.

  17. Phosphonic acid based exchange resins

    DOEpatents

    Horwitz, E.P.; Alexandratos, S.D.; Gatrone, R.C.; Chiarizia, R.

    1995-09-12

    An ion exchange resin is described for extracting metal ions from a liquid waste stream. An ion exchange resin is prepared by copolymerizing a vinylidene diphosphonic acid with styrene, acrylonitrile and divinylbenzene. 10 figs.

  18. Epoxy resin holograms

    NASA Astrophysics Data System (ADS)

    Ruiz-Limón, B.; Wetzel, G. B. J.; Olivares Pérez, A.; Ponce-Lee, E. L.; Ramos-Garcia, R.; Toxqui López, S.; Hernández-Garay, M. P.; Fuentes-Tapia, I.

    2006-02-01

    We observed that a commercial epoxy resin (Comex (R) is enable to record images by means of lithography techniques. We can generate a hologram using a digital image and a computer simulation program and transferred it on our resin by microlithography techniques to get a phase hologram and increase its efficiency. The exposition to the heat produce temperature gradients and the information in the mask is transferred to the material by the refraction index changes, thus the film is recorded. At the same time the hologram is cured.

  19. Resin impregnation process for producing a resin-fiber composite

    NASA Technical Reports Server (NTRS)

    Palmer, Raymond J. (Inventor); Moore, William E. (Inventor)

    1994-01-01

    Process for vacuum impregnation of a dry fiber reinforcement with a curable resin to produce a resin-fiber composite, by drawing a vacuum to permit flow of curable liquid resin into and through a fiber reinforcement to impregnate same and curing the resin-impregnated fiber reinforcement at a sufficient temperature and pressure to effect final curing. Both vacuum and positive pressure, e.g. autoclave pressure, are applied to the dry fiber reinforcement prior to application of heat and prior to any resin flow to compact the dry fiber reinforcement, and produce a resin-fiber composite of reduced weight, thickness and resin content, and improved mechanical properties. Preferably both a vacuum and positive pressure, e.g. autoclave pressure, are also applied during final curing.

  20. Nontoxic Resins Advance Aerospace Manufacturing

    NASA Technical Reports Server (NTRS)

    2009-01-01

    The 2008 NASA Commercial Invention of the Year, PETI-330, is a polyimide matrix resin that performs well at high temperatures and is easily processed into composites in a simple, short curing cycle. Invented by scientists at Langley Research Center, PETI-330 is now licensed to Ube Industries, based in Japan with its American headquarters in New York. In addition to being durable and lightweight, the resin is also nontoxic, which makes it safe for workers to handle. PETI-330 was created specifically for heat-resistant composites formed with resin transfer molding and resin infusion, which formerly could only be used with low temperature resin systems.

  1. High-temperature resins

    NASA Technical Reports Server (NTRS)

    Serafini, T. T.

    1982-01-01

    The basic chemistry, cure processes, properties, and applications of high temperature resins known as polyimides are surveyed. Condensation aromatic polymides are prepared by reacting aromatic diamines with aromatic dianhydrides, aromatic tetracarboxylic acids, or with dialkyl esters of aromatic tetracarboxylic acids, depending on the intended end use. The first is for coatings or films while the latter two are more suitable for polyimide matrix resins. Prepreg solutions are made by dissolving reactants in an aprotic solvent, and advances in the addition of a diamine on the double bond and radical polymerization of the double bond are noted to have yielded a final cure product with void-free characteristics. Attention is given to properties of the Skybond, Pyralin, and NR-150B polyimide prepreg materials and characteristics of aging in the NP-150 polyimides. Finally, features of the NASA-developed PMR polyimides are reviewed.

  2. Flame Retardant Epoxy Resins

    NASA Technical Reports Server (NTRS)

    Thompson, C. M.; Smith, J. G., Jr.; Connell, J. W.; Hergenrother, P. M.; Lyon, R. E.

    2004-01-01

    As part of a program to develop fire resistant exterior composite structures for future subsonic commercial aircraft, flame retardant epoxy resins are under investigation. Epoxies and their curing agents (aromatic diamines) containing phosphorus were synthesized and used to prepare epoxy formulations. Phosphorus was incorporated within the backbone of the epoxy resin and not used as an additive. The resulting cured epoxies were characterized by thermogravimetric analysis, propane torch test, elemental analysis and microscale combustion calorimetry. Several formulations showed excellent flame retardation with phosphorous contents as low as 1.5% by weight. The fracture toughness of plaques of several cured formulations was determined on single-edge notched bend specimens. The chemistry and properties of these new epoxy formulations are discussed.

  3. Bismaleimide Copolymer Matrix Resins

    NASA Technical Reports Server (NTRS)

    Parker, John A.; Heimbuch, Alvin H.; Hsu, Ming-Ta S.; Chen, Timothy S.

    1987-01-01

    Graphite composites, prepared from 1:1 copolymer of two new bismaleimides based on N,N'-m-phenylene-bis(m-amino-benzamide) structure have mechanical properties superior to those prepared from other bismaleimide-type resins. New heat-resistant composites replace metal in some structural applications. Monomers used to form copolymers with superior mechanical properties prepared by reaction of MMAB with maleic or citraconic anhydride.

  4. Production of large quantities of 90Y by ion-exchange chromatography using an organic resin and a chelating agent.

    PubMed

    Castillo, Abmel Xiques; Pérez-Malo, Marylaine; Isaac-Olivé, Keila; Mukhallalati, Heyam; González, Edgar Casanova; Berdeguez, Mirta Torres; Díaz, Néstor Cornejo

    2010-11-01

    The performance of a system composed of an organic cation exchanger (Dowex 50Wx8) and a chelating agent (EDTA) previously described for the successful production of (90)Y via a (90)Sr/(90)Y generator is assessed under dynamic conditions. In an attempt to overcome the established limitation of ion-exchange resins for the separation of subcurie quantities of activity, (90)Y is repeatedly isolated from an 11.8-GBq (320 mCi) (90)Sr cow using a three-column tandem arrangement. The high recovery and radionuclidic purity obtained for (90)Y and the parameters of the separation (time, eluant concentration, pH and flow rate range) strongly suggest that Ci quantities of (90)Y can be handled satisfactorily by the ion-exchange method. No replacement or treatment of the cow, low waste generation and (90)Sr losses less than 0.1% after each run were observed during the present study which, in combination with the low cost of this resin, may result in an attractive alternate method for the production of large quantities of (90)Y. PMID:21055624

  5. System for removing contaminants from plastic resin

    DOEpatents

    Bohnert, George W.; Hand, Thomas E.; DeLaurentiis, Gary M.

    2010-11-23

    A resin recycling system that produces essentially contaminant-free synthetic resin material in an environmentally safe and economical manner. The system includes receiving the resin in container form. A grinder grinds the containers into resin particles. The particles are exposed to a solvent in one or more solvent wash vessels, the solvent contacting the resin particles and substantially removing contaminants on the resin particles. A separator is used to separate the resin particles and the solvent. The resin particles are then placed in solvent removing element where they are exposed to a solvent removing agent which removes any residual solvent remaining on the resin particles after separation.

  6. Advanced thermoplastic resins, phase 1

    NASA Technical Reports Server (NTRS)

    Hendricks, C. L.; Hill, S. G.; Falcone, A.; Gerken, N. T.

    1991-01-01

    Eight thermoplastic polyimide resin systems were evaluated as composite matrix materials. Two resins were selected for more extensive mechanical testing and both were versions of LaRC-TPI (Langley Research Center - Thermoplastic Polyimide). One resin was made with LaRC-TPI and contained 2 weight percent of a di(amic acid) dopant as a melt flow aid. The second system was a 1:1 slurry of semicrystalline LaRC-TPI powder in a polyimidesulfone resin diglyme solution. The LaRC-TPI powder melts during processing and increases the melt flow of the resin. Testing included dynamic mechanical analysis, tension and compression testing, and compression-after-impact testing. The test results demonstrated that the LaRC-TPI resins have very good properties compared to other thermoplastics, and that they are promising matrix materials for advanced composite structures.

  7. Vitrification of ion exchange resins

    DOEpatents

    Cicero-Herman, Connie A.; Workman, Rhonda Jackson

    2001-01-01

    The present invention relates to vitrification of ion exchange resins that have become loaded with hazardous or radioactive wastes, in a way that produces a homogenous and durable waste form and reduces the disposal volume of the resin. The methods of the present invention involve directly adding borosilicate glass formers and an oxidizer to the ion exchange resin and heating the mixture at sufficient temperature to produce homogeneous glass.

  8. Phosphorus-containing bisimide resins

    NASA Technical Reports Server (NTRS)

    Varma, I. K.; Fohlen, G. M.; Parker, J. A. (Inventor)

    1981-01-01

    The production of fire-resistant resins particularly useful for making laminates with inorganic fibers such as graphite fibers is discussed. The resins are by (1) condensation of an ethylenically unsaturated cyclic anhydride with a bis(diaminophenyl) phosphine oxide, and (2) by addition polymerization of the bisimide so obtained. Up to about 50%, on a molar basis, of benzophenonetetracarboxylic acid anhydride can be substituted for some of the cyclic anhydride to alter the properties of the products. Graphite cloth laminates made with these resins show 800 C char yields greater than 70% by weight in nitrogen. Limiting oxygen indexes of more than 100% are determined for these resins.

  9. A new polyimide laminatine resin

    NASA Technical Reports Server (NTRS)

    Barrick, J. D. W.; Jewell, R. A.; Stclair, T. L.

    1977-01-01

    Addition polyimide for composite materials is based on liquid monomers and has significant advantages over most existing high-temperature resins. Essentially solventless prepreg has improved drape, tack.

  10. 40 CFR 414.50 - Applicability; description of the thermosetting resins subcategory.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... the products classified under SIC 28214 thermosetting resins including those resins and resin groups listed below. Product groups are indicated with an asterisk (*). *Alkyd Resins Dicyanodiamide Resin *Epoxy Resins *Fumaric Acid Polyesters *Furan Resins Glyoxal-Urea Formaldehyde Textile Resin...

  11. 40 CFR 414.50 - Applicability; description of the thermosetting resins subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... the products classified under SIC 28214 thermosetting resins including those resins and resin groups listed below. Product groups are indicated with an asterisk (*). *Alkyd Resins Dicyanodiamide Resin *Epoxy Resins *Fumaric Acid Polyesters *Furan Resins Glyoxal-Urea Formaldehyde Textile Resin...

  12. 40 CFR 414.50 - Applicability; description of the thermosetting resins subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... the products classified under SIC 28214 thermosetting resins including those resins and resin groups listed below. Product groups are indicated with an asterisk (*). *Alkyd Resins Dicyanodiamide Resin *Epoxy Resins *Fumaric Acid Polyesters *Furan Resins Glyoxal-Urea Formaldehyde Textile Resin...

  13. 40 CFR 414.50 - Applicability; description of the thermosetting resins subcategory.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... the products classified under SIC 28214 thermosetting resins including those resins and resin groups listed below. Product groups are indicated with an asterisk (*). *Alkyd Resins Dicyanodiamide Resin *Epoxy Resins *Fumaric Acid Polyesters *Furan Resins Glyoxal-Urea Formaldehyde Textile Resin...

  14. 40 CFR 414.50 - Applicability; description of the thermosetting resins subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... the products classified under SIC 28214 thermosetting resins including those resins and resin groups listed below. Product groups are indicated with an asterisk (*). *Alkyd Resins Dicyanodiamide Resin *Epoxy Resins *Fumaric Acid Polyesters *Furan Resins Glyoxal-Urea Formaldehyde Textile Resin...

  15. Imide modified epoxy matrix resins

    NASA Technical Reports Server (NTRS)

    Scola, D. A.; Pater, R. H.

    1981-01-01

    High char yield epoxy using novel bisimide amines (BIA's) as curing agents with a state of the art epoxy resin was developed. Stoichiometric quantities of the epoxy resin and the BIA's were studied to determine the cure cycle required for preparation of resin specimens. The bisimide cured epoxies were designated IME's (imide modified epoxy). The physical, thermal and mechanical properties of these novel resins were determined. The levels of moisture absorption exhibited by the bisimide amine cured expoxies (IME's) were considerably lower than the state of the art epoxies. The strain-to-failure of the control resin system was improved 25% by replacement of DDS with 6F-DDS. Each BIA containing resin exhibited twice the char yield of the control resin MY 720/DDS. Graphite fiber reinforced control (C) and IME resins were fabricated and characterized. Two of the composite systems showed superior properties compared to the other Celion 6000/IME composite systems and state of the art graphite epoxy systems. The two systems exhibited excellent wet shear and flexural strengths and moduli at 300 and 350 F.

  16. Resin composite repair: Quantitative microleakage evaluation of resin-resin and resin-tooth interfaces with different surface treatments

    PubMed Central

    Celik, Cigdem; Cehreli, Sevi Burcak; Arhun, Neslihan

    2015-01-01

    Objective: The aim was to evaluate the effect of different adhesive systems and surface treatments on the integrity of resin-resin and resin-tooth interfaces after partial removal of preexisting resin composites using quantitative image analysis for microleakage testing protocol. Materials and Methods: A total of 80 human molar teeth were restored with either of the resin composites (Filtek Z250/GrandioSO) occlusally. The teeth were thermocycled (1000×). Mesial and distal 1/3 parts of the restorations were removed out leaving only middle part. One side of the cavity was finished with course diamond bur and the other was air-abraded with 50 μm Al2O3. They were randomly divided into four groups (n = 10) to receive: Group 1: Adper Single Bond 2; Group 2: All Bond 3; Group 3: ClearfilSE; Group 4: BeautiBond, before being repaired with the same resin composite (Filtek Z250). The specimens were re-thermocycled (1000×), sealed with nail varnish, stained with 0.5% basic fuchsin, sectioned mesiodistally and photographed digitally. The extent of dye penetration was measured by image analysis software (ImageJ) for both bur-finished and air-abraded surfaces at resin-tooth and resin-resin interfaces. The data were analyzed statistically. Results: BeautiBond exhibited the most microleakage at every site. Irrespective of adhesive and initial composite type, air-abrasion showed less microleakage except for BeautiBond. The type of initial repaired restorative material did not affect the microleakage. BeautiBond adhesive may not be preferred in resin composite repair in terms of microleakage prevention. Conclusions: Surface treatment with air-abrasion produced the lowest microleakage scores, independent of the adhesive systems and the pre-existing resin composite type. Pre-existing composite type does not affect the microleakage issue. All-in-one adhesive resin (BeautiBond) may not be preferred in resin composite repair in terms of microleakage prevention. PMID:25713491

  17. Chromatography resin support

    DOEpatents

    Dobos, James G.

    2002-01-01

    An apparatus and method of using an improved chromatography resin support is disclosed. The chromatography support platform is provided by a stainless steel hollow cylinder adapted for being inserted into a chromatography column. An exterior wall of the stainless steel cylinder defines a groove for carrying therein an "O"-ring. The upper surface of the stainless steel column is covered by a fine stainless steel mesh welded to the edges of the stainless steel cylinder. When placed upon a receiving ledge defined within a chromatography column, the "O"-ring provides a fluid tight seal with the inner edge wall of the chromatography cylinder. The stainless steel mesh supports the chromatography matrix and provides a back flushable support which is economical and simple to construct.

  18. Indirect resin composites

    PubMed Central

    Nandini, Suresh

    2010-01-01

    Aesthetic dentistry continues to evolve through innovations in bonding agents, restorative materials, and conservative preparation techniques. The use of direct composite restoration in posterior teeth is limited to relatively small cavities due to polymerization stresses. Indirect composites offer an esthetic alternative to ceramics for posterior teeth. This review article focuses on the material aspect of the newer generation of composites. This review was based on a PubMed database search which we limited to peer-reviewed articles in English that were published between 1990 and 2010 in dental journals. The key words used were ‘indirect resin composites,’ composite inlays,’ and ‘fiber-reinforced composites.’ PMID:21217945

  19. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Terpene resins. 178.3930 Section 178.3930 Food and... and Production Aids § 178.3930 Terpene resins. The terpene resins identified in paragraph (a) of this... the terpene resins identified in paragraph (b) of this section may be safely used as components...

  20. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Terpene resins. 178.3930 Section 178.3930 Food and... and Production Aids § 178.3930 Terpene resins. The terpene resins identified in paragraph (a) of this... the terpene resins identified in paragraph (b) of this section may be safely used as components...

  1. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Terpene resins. 178.3930 Section 178.3930 Food and... and Production Aids § 178.3930 Terpene resins. The terpene resins identified in paragraph (a) of this... the terpene resins identified in paragraph (b) of this section may be safely used as components...

  2. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Terpene resins. 178.3930 Section 178.3930 Food and... and Production Aids § 178.3930 Terpene resins. The terpene resins identified in paragraph (a) of this... the terpene resins identified in paragraph (b) of this section may be safely used as components...

  3. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Terpene resins. 178.3930 Section 178.3930 Food and... Terpene resins. The terpene resins identified in paragraph (a) of this section may be safely used as components of polypropylene film intended for use in contact with food, and the terpene resins identified...

  4. Resin polymerization problems--are they caused by resin curing lights, resin formulations, or both?

    PubMed

    Christensen, R P; Palmer, T M; Ploeger, B J; Yost, M P

    1999-01-01

    Negative effects of rapid, high-intensity resin curing have been predicted for both argon lasers and plasma-arc curing lights. To address these questions, six different resin restorative materials were cured with 14 different resin curing lights representing differences in intensities ranging from 400 mW/cm2 to 1,900 mW/cm2; delivery modes using constant, ramped, and stepped methods; cure times ranging from 1 second to 40 seconds; and spot sizes of 6.7 mm to 10.9 mm. Two lasers, five plasma-arc lights, and seven halogen lights were used. Shrinkage, modulus, heat generation, strain, and physical changes on the teeth and resins during strain testing were documented. Results showed effects associated with lights were not statistically significant, but resin formulation was highly significant. Microfill resins had the least shrinkage and the lowest modulus. An autocure resin had shrinkage and modulus as high as or higher than the light-cured hybrid resins. Lasers and plasma-arc lights produced the highest heat increases on the surface (up to 21 degrees C) and within the resin restorations (up to 14 degrees C), and the halogen lights produced the most heat within the pulp chamber (up to 2 degrees C). Strain within the tooth was least with Heliomolar and greatest with Z100 Restorative and BISFIL II autocure resin. Clinical effects of strain relief were evident as white lines at the tooth-resin interface and cracks in enamel adjacent to the margins. This work implicates resin formulation, rather than light type or curing mode, as the important factor in polymerization problems. Lower light intensity and use of ramped and stepped curing modes did not provide significant lowering of shrinkage, modulus, or strain, and did not prevent enamel cracking adjacent to margins and formation of "white line" defects at the margins. Until materials with lower shrinkage and modulus are available, use of low-viscosity surface sealants as a final step in resin placement is suggested to

  5. Resin/graphite fiber composites

    NASA Technical Reports Server (NTRS)

    Cavano, P. J.; Jones, R. J.; Vaughan, R. W.

    1972-01-01

    High temperature resin matrices suitable for use in advanced graphite fiber composites for jet engine applications were evaluated. A series of planned, sequential screening experiments with resin systems in composite form were performed to reduce the number of candidates to a single A-type polyimide resin that repetitively produced void-free, high strength and modulus composites acceptable for use in the 550 F range for 1000 hours. An optimized processing procedure was established for this system. Extensive mechanical property studies characterized this single system, at room temperature, 500 F, 550 F and 600 F, for various exposure times.

  6. Flammability screening tests of resins

    NASA Technical Reports Server (NTRS)

    Arhart, R. W.; Farrar, D. G.; Hughes, B. M.

    1979-01-01

    Selected flammability characteristics of glass cloth laminates of thermosetting resins are evaluated. A protocol for the evaluation of the flammability hazards presented by glass cloth laminates of thermosetting resins and the usefulness of that protocol with two laminates are presented. The glass laminates of an epoxy resin, M-751 are evaluated for: (1) determination of smoke generation from the laminates; (2) analysis of products of oxidative degradation of the laminates; (3) determination of minimum oxygen necessary to maintain flaming oxidation; (4) evaluation of toxicological hazards.

  7. Grafted methylenediphosphonate ion exchange resins

    DOEpatents

    Trochimcznk, A.W.; Gatrone, R.C.; Alexandratos, S.; Horwitz, E.P.

    1997-04-08

    An ion exchange resin is disclosed that is comprised of an insoluble copolymer onto which are grafted pendent groups that provide 1.0 to about 10 mmol/g dry weight phosphorus. The pendent groups have the formula as shown in the patent wherein R is hydrogen, a cation or mixtures thereof; and R{sup 1} is hydrogen or an C{sub 1}-C{sub 2} alkyl group. The resin also contains zero to about 5 mmol/g dry weight of pendent aromatic sulfonate groups. Processes for making and using an ion exchange resin are also disclosed.

  8. Grafted methylenediphosphonate ion exchange resins

    DOEpatents

    Trochimcznk, Andrzej W.; Gatrone, Ralph C.; Alexandratos, Spiro; Horwitz, E. Philip

    1997-01-01

    An ion exchange resin is disclosed that is comprised of an insoluble copolymer onto which are grafted pendent groups that provide 1.0 to about 10 mmol/g dry weight phosphorous. The pendent groups have the formula ##STR1## wherein R is hydrogen, a cation or mixtures thereof; and R.sup.1 is hydrogen or an C.sub.1 -C.sub.2 alkyl group. The resin also contains zero to about 5 mmol/g dry weight of pendent aromatic sulfonate groups. Processes for making and using an ion exchange resin are also disclosed.

  9. Grafted methylenediphosphonate ion exchange resins

    DOEpatents

    Trochimcznk, Andrzej W.; Gatrone, Ralph C.; Alexandratos, Spiro; Horwitz, E. Philip

    1998-01-27

    An ion exchange resin is disclosed that is comprised of an insoluble copolymer onto which are grafted pendent groups that provide 1.0 to about 10 mmol/g dry weight phosphorous. The pendent groups have the formula ##STR1## wherein R is hydrogen, a cation or mixtures thereof; and R.sup.1 is hydrogen or an C.sub.1 -C.sub.2 alkyl group. The resin also contains zero to about 5 mmol/g dry weight of pendent aromatic sulfonate groups. Processes for making and using an ion exchange-resin are also disclosed.

  10. Regenerating Water-Sterilizing Resins

    NASA Technical Reports Server (NTRS)

    Colombo, G. V.; Putnam, D. F.

    1982-01-01

    Iodine-dispensing resin can be regenerated after iodine content has been depleted, without being removed from water system. Resin is used to make water potable by killing bacteria, fungi, and viruses. Regeneration technique may be come basis of water purifier for very long space missions. Enough crystalline iodine for multiple regenerations during mission can be stored in one small cartridge. Cartridge could be inserted in waterline as necessary on signal from iodine monitor or timer.

  11. Liquid monobenzoxazine based resin system

    DOEpatents

    Tietze, Roger; Nguyen, Yen-Loan; Bryant, Mark

    2014-10-07

    The present invention provides a liquid resin system including a liquid monobenzoxazine monomer and a non-glycidyl epoxy compound, wherein the weight ratio of the monobenzoxazine monomer to the non-glycidyl epoxy compound is in a range of about 25:75 to about 60:40. The liquid resin system exhibits a low viscosity and exceptional stability over an extended period of time making its use in a variety of composite manufacturing methods highly advantageous.

  12. 50W CW output power and 12mJ pulses from a quasi-2-level Yb:YAG ceramic rod laser end-pumped at the 969nm zero-phonon line

    NASA Astrophysics Data System (ADS)

    Fries, Christian; Weitz, Marco; Theobald, Christian; v. Löwis of Menar, Patric; Bartschke, Jürgen; L'huillier, Johannes A.

    2015-02-01

    With the advent of high power and narrow bandwidth 969 nm pump diodes, direct pumping into the upper laser level of Yb:YAG and hence quasi-2-level lasers became possible. Pumping directly into the emitting level leads to higher quantum efficiency and reduction of non-radiative decay. Consequently, thermal load, thermal lensing and risk of fracture are reduced significantly. Moreover pump saturation and thermal population of uninvolved energy-levels in ground and excited states are benefical for a homogenous distribution of the pump beam as well as the reduction of reabsorption loss compared to 3-level systems, which allows for high-power DPSS lasers. Beside continuous-wave (cw) operation, nanosecond pulses with a repetition rate between 1 and 5 kHz are an attractive alternative to flashlamp-pumped systems (10-100 Hz) in various measurement applications that require higher data acquisition rates because of new faster detectors. Based on measurements of the absorption and a detailed numerical model for pump beam distribution, including beam propagation and saturation factors, power-scaling of a ceramic rod Yb:YAG oscillator was possible. Finally a cw output power of 50 W with 33 % pump efficiency at 1030 nm has been demonstrated (M2 < 1.2). Nanosecond pulses have been produced by cavity-dumping of this system. The cavity-dumped setup allowed for 3-10 ns pulses with a pulse energy of 12.5 mJ at 1 kHz (M2 < 1.1). In order to achieve these results a systematic experimental and numerical investigation on gain dynamics and the identification of different stable operating regimes has been carried out.

  13. Maleimide Functionalized Siloxane Resins

    SciTech Connect

    Loy, D.A.; Shaltout, R.M.

    1999-04-01

    Polyorganosiloxanes are a commercially important class of compounds. They exhibit many important properties, including very low glass transition temperatures, making them useful over a wide temperature range. In practice, the polysiloxane polymer is often mixed with a filler material to help improve its mechanical properties. An alternative method for increasing polymer mechanical strength is through the incorporation of certain substituents on the polymer backbone. Hard substituents such as carbonates and imides generally result in improved mechanical properties of polysiloxanes. In this paper, we present the preparation of novel polysiloxane resins modified with hard maleimide substituents. Protected ethoxysilyl-substituted propyl-maleimides were prepared. The maleimide substituent was protected with a furanyl group and the monomer polymerized under aqueous acidic conditions. At elevated temperatures (>120 C), the polymer undergoes retro Diels-Alder reaction with release of foran (Equation 1). The deprotected polymer can then be selectively crosslinked by a forward Diels-Alder reaction (in the presence of a co-reactant having two or more dime functionalities).

  14. Low Melt Viscosity Resins for Resin Transfer Molding

    NASA Technical Reports Server (NTRS)

    Harris, Frank W.

    2002-01-01

    In recent years, resin transfer molding (RTM) has become one of the methods of choice for high performance composites. Its cost effectiveness and ease of fabrication are major advantages of RTM. RTM process usually requires resins with very low melt viscosity (less than 10 Poise). The optimum RTM resins also need to display high thennal-oxidative stability, high glass transition temperature (T(sub g)), and good toughness. The traditional PMR-type polyimides (e.g. PMR-15) do not fit this requirement, because the viscosities are too high and the nadic endcap cures too fast. High T(sub g), low-melt viscosity resins are highly desirable for aerospace applications and NASA s Reusable Launch Vehicle (RLV) program. The objective of this work is to prepare low-melt viscosity polyimide resins for RTM or resin film infusion (RFI) processes. The approach involves the synthesis of phenylethynyl-terminated imide oligomers. These materials have been designed to minimize their melt viscosity so that they can be readily processed. During the cure, the oligomers undergo both chain extension and crosslinking via the thermal polymerization of the phenylethynyl groups. The Phenylethynyl endcap is preferred over the nadic group due to its high curing temperature, which provides broader processing windows. This work involved the synthesis and polymerization of oligomers containing zig-zag backbones and twisted biphenyl structures. Some A-B type precursors which possessed both nitro and anhydride functionality, or both nitro and amine functionality, were also synthesized in order to obtain the well defined oligomers. The resulting zig-zag structured oligomers were then end-capped with 4-phenylethynylphthalic anhydride (PEPA) for further cure. The properties of these novel imide oligomers are evaluated.

  15. Protection of dried probiotic bacteria from bile using bile adsorbent resins.

    PubMed

    Mahbubani, Krishnaa T; Slater, Nigel K H; Edwards, Alexander D

    2014-01-25

    Enteric coated oral tablets or capsules can deliver dried live cells directly into the intestine. Previously, we found that a live attenuated bacterial vaccine acquired sensitivity to intestinal bile when dried, raising the possibility that although gastric acid can be bypassed, significant loss of viability might occur on release from an enteric coated oral formulations. Here we demonstrate that some food-grade lyophilised preparations of Lactobacillus casei and Lactobacillus salivarius also show temporary bile sensitivity that can be rapidly reversed by rehydration. To protect dried bacterial cells from temporary bile sensitivity, we propose using bile acid adsorbing resins, such as cholestyramine, which are bile acid binding agents, historically used to lower cholesterol levels. Vcaps™ HPMC capsules alone provided up to 830-fold protection from bile. The inclusion of 50% w/w cholestyramine in Vcaps™ HPMC capsules resulted in release of up to 1700-fold more live Lactobacillus casei into simulated intestinal fluid containing 1% bile, when compared to dried cells added directly to bile. We conclude that delivery of dried live probiotic organisms to the intestine may be improved by providing protection from bile by addition of bile adsorbing resins and the use of HPMC capsules. PMID:24080386

  16. Phosphonic acid based ion exchange resins

    DOEpatents

    Horwitz, E. Philip; Alexandratos, Spiro D.; Gatrone, Ralph C.; Chiarizia, Ronato

    1996-01-01

    An ion exchange resin for extracting metal ions from a liquid waste stream. An ion exchange resin is prepared by copolymerizing a vinylidene diphosphonic acid with styrene, acrylonitrile and divinylbenzene.

  17. Phosphonic acid based ion exchange resins

    DOEpatents

    Horwitz, E. Philip; Alexandratos, Spiro D.; Gatrone, Ralph C.; Chiarizia, Ronato

    1994-01-01

    An ion exchange resin for extracting metal ions from a liquid waste stream. An ion exchange resin is prepared by copolymerizing a vinylidene disphosphonic acid with styrene, acrylonitrile and divinylbenzene.

  18. Soluble high molecular weight polyimide resins

    NASA Technical Reports Server (NTRS)

    Jones, R. J.; Lubowitz, H. R.

    1970-01-01

    High molecular weight polyimide resins have greater than 20 percent /by weight/ solubility in polar organic solvents. They permit fabrication into films, fibers, coatings, reinforced composite, and adhesive product forms. Characterization properties for one typical polyimide resin are given.

  19. Phosphonic acid based ion exchange resins

    DOEpatents

    Horwitz, E.P.; Alexandratos, S.D.; Gatrone, R.C.; Chiarizia, R.

    1994-01-25

    An ion exchange resin is described for extracting metal ions from a liquid waste stream. An ion exchange resin is prepared by copolymerizing a vinylidene diphosphonic acid with styrene, acrylonitrile and divinylbenzene. 9 figures.

  20. Phosphonic acid based ion exchange resins

    DOEpatents

    Horwitz, E.P.; Alexandratos, S.D.; Gatrone, R.C.; Chiarizia, R.

    1996-07-23

    An ion exchange resin is described for extracting metal ions from a liquid waste stream. An ion exchange resin is prepared by copolymerizing a vinylidene diphosphonic acid with styrene, acrylonitrile and divinylbenzene. 10 figs.

  1. Method for loading resin beds

    DOEpatents

    Notz, Karl J.; Rainey, Robert H.; Greene, Charles W.; Shockley, William E.

    1978-01-01

    An improved method of preparing nuclear reactor fuel by carbonizing a uranium loaded cation exchange resin provided by contacting a H.sup.+ loaded resin with a uranyl nitrate solution deficient in nitrate, comprises providing the nitrate deficient solution by a method comprising the steps of reacting in a reaction zone maintained between about 145.degree.-200.degree. C, a first aqueous component comprising a uranyl nitrate solution having a boiling point of at least 145.degree. C with a second aqueous component to provide a gaseous phase containing HNO.sub.3 and a reaction product comprising an aqueous uranyl nitrate solution deficient in nitrate.

  2. 21 CFR 172.280 - Terpene resin.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Terpene resin. 172.280 Section 172.280 Food and... Terpene resin. The food additive terpene resin may be safely used in accordance with the following prescribed conditions: (a) The food additive is the betapinene polymer obtained by polymerizing...

  3. 21 CFR 172.280 - Terpene resin.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Terpene resin. 172.280 Section 172.280 Food and..., Films and Related Substances § 172.280 Terpene resin. The food additive terpene resin may be safely used... polymer obtained by polymerizing terpene hydrocarbons derived from wood. It has a softening point of...

  4. 21 CFR 172.280 - Terpene resin.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Terpene resin. 172.280 Section 172.280 Food and..., Films and Related Substances § 172.280 Terpene resin. The food additive terpene resin may be safely used... polymer obtained by polymerizing terpene hydrocarbons derived from wood. It has a softening point of...

  5. 21 CFR 172.280 - Terpene resin.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Terpene resin. 172.280 Section 172.280 Food and..., Films and Related Substances § 172.280 Terpene resin. The food additive terpene resin may be safely used... polymer obtained by polymerizing terpene hydrocarbons derived from wood. It has a softening point of...

  6. 21 CFR 172.280 - Terpene resin.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Terpene resin. 172.280 Section 172.280 Food and..., Films and Related Substances § 172.280 Terpene resin. The food additive terpene resin may be safely used... polymer obtained by polymerizing terpene hydrocarbons derived from wood. It has a softening point of...

  7. 21 CFR 177.1550 - Perfluorocarbon resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    .... Perfluorocarbon resins can be identified by their characteristic infrared spectra. (2) Melt-viscosity. (i) The per-fluoro-carbon resins identified in paragraph (a)(1) of this section shall have a melt viscosity of not... viscosity of the perfluorocarbon resins identified in paragraph (a)(1) of this section shall not vary...

  8. 21 CFR 177.1550 - Perfluorocarbon resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    .... Perfluorocarbon resins can be identified by their characteristic infrared spectra. (2) Melt-viscosity. (i) The per-fluoro-carbon resins identified in paragraph (a)(1) of this section shall have a melt viscosity of not... viscosity of the perfluorocarbon resins identified in paragraph (a)(1) of this section shall not vary...

  9. 21 CFR 177.1550 - Perfluorocarbon resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    .... Perfluorocarbon resins can be identified by their characteristic infrared spectra. (2) Melt-viscosity. (i) The per-fluoro-carbon resins identified in paragraph (a)(1) of this section shall have a melt viscosity of not... viscosity of the perfluorocarbon resins identified in paragraph (a)(1) of this section shall not vary...

  10. Method for removing contaminants from plastic resin

    DOEpatents

    Bohnert, George W.; Hand, Thomas E.; DeLaurentiis, Gary M.

    2008-12-30

    A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

  11. Method of removing contaminants from plastic resins

    DOEpatents

    Bohnert,George W.; Hand,Thomas E.; Delaurentiis,Gary M.

    2007-08-07

    A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

  12. Method of removing contaminants from plastic resins

    DOEpatents

    Bohnert, George W.; Hand, Thomas E.; DeLaurentiis, Gary M.

    2008-11-18

    A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

  13. Process for curing bismaleimide resins

    NASA Technical Reports Server (NTRS)

    Parker, John A. (Inventor); OTHY S.imides alone. (Inventor)

    1986-01-01

    This invention relates to vinyl pyridine group containing compounds and oligomers, their advantageous copolymerization with bismaleimide resins, and the formation of reinforced composites based on these copolymers. When vinyl pyridines including vinyl stilbazole materials and vinyl styrylpyridine oligomer materials are admixed with bismaleimides and cured to form copolymers the cure temperatures of the copolymers are substantially below the cure temperatures of the bismaleimides alone.

  14. Synthesis of improved phenolic resins

    NASA Technical Reports Server (NTRS)

    Delano, C. B.; Mcleod, A. H.

    1979-01-01

    Twenty seven addition cured phenolic resin compositions were prepared and tested for their ability to give char residues comparable to state-of-the-art phenolic resins. Cyanate, epoxy, allyl, acrylate, methacrylate and ethynyl derivatized phenolic oligomers were investigated. The novolac-cyanate and propargyl-novolac resins provided anaerobic char yields at 800 C of 58 percent. A 59 percent char yield was obtained from modified epoxy novolacs. A phosphonitrilic derivative was found to be effective as an additive for increasing char yields. The novolac-cyanate, epoxy-novolac and methacrylate-epoxy-novolac systems were investigated as composite matrices with Thornel 300 graphite fiber. All three resins showed good potential as composite matrices. The free radical cured methacrylate-epoxy-novolac graphite composite provided short beam shear strengths at room temperature of 93.3 MPa (13.5 ksi). The novolac-cyanate graphite composite produced a short beam shear strength of 74 MPa (10.7 ksi) and flexural strength of 1302 MPa (189 ksi) at 177 C. Air heat aging of the novolac-cyanate and epoxy novolac based composites for 12 weeks at 204 C showed good property retention.

  15. Fiber reinforced composite resin systems.

    PubMed

    Giordano, R

    2000-01-01

    The Targis/Vectris and Sculpture/FibreKor systems were devised to create a translucent maximally reinforced resin framework for fabrication of crowns, bridges, inlays, and onlays. These materials are esthetic, have translucency similar to castable glass-ceramics such as OPC and Empress, and have fits that are reported to be acceptable in clinical and laboratory trials. These restorations rely on proper bonding to the remaining tooth structure; therefore, careful attention to detail must be paid to this part of the procedure. Cementation procedures should involve silane treatment of the cleaned abraded internal restoration surface, application of bonding agent to the restoration as well as the etched/primed tooth, and finally use of a composite resin. Each manufacturer has a recommended system which has been tested for success with its resin system. These fiber reinforced resins are somewhat different than classical composites, so not all cementation systems will necessarily work with them. Polishing of the restoration can be accomplished using diamond or alumina impregnated rubber wheels followed by diamond paste. The glass fibers can pose a health risk. They are small enough to be inhaled and deposited in the lungs, resulting in a silicosis-type problem. Therefore, if fibers are exposed and ground on, it is extremely important to wear a mask. Also, the fibers can be a skin irritant, so gloves also should be worn. If the fibers become exposed intraorally, they can cause gingival inflammation and may attract plaque. The fibers should be covered with additional composite resin. If this cannot be accomplished, the restoration should be replaced. The bulk of these restorations are formed using a particulate filled resin, similar in structure to conventional composite resins. Therefore, concerns as to wear resistance, color stability, excessive expansion/contraction, and sensitivity remain until these materials are proven in long-term clinical trials. They do hold the

  16. Oxygen index tests of thermosetting resins

    NASA Technical Reports Server (NTRS)

    Gilwee, W. J., Jr.; Parker, J. A.; Kourtides, D. A.

    1980-01-01

    The flammability characteristics of nine thermosetting resins under evaluation for use in aircraft interiors are described. These resins were evaluated using the Oxygen Index (ASTM 2863) testing procedure. The test specimens consisted of both neat resin and glass reinforced resin. When testing glass-reinforced samples it was observed that Oxygen Index values varied inversely with resin content. Oxygen values were also obtained on specimens exposed to temperatures up to 300 C. All specimens experienced a decline in Oxygen Index when tested at an elevated temperature.

  17. Commercial Ion Exchange Resin Vitrification Studies

    SciTech Connect

    Cicero-Herman, C.A

    2002-06-28

    In the nuclear industry, ion exchange resins are used for purification of aqueous streams. The major contaminants of the resins are usually the radioactive materials that are removed from the aqueous streams. The use of the ion exchange resins creates a waste stream that can be very high in both organic and radioactive constituents. Therefore, disposal of the spent resin often becomes an economic problem because of the large volumes of resin produced and the relatively few technologies that are capable of economically stabilizing this waste. Vitrification of this waste stream presents a reasonable disposal alternative because of its inherent destruction capabilities, the volume reductions obtainable, and the durable product that it produces.

  18. Phenoxy resins containing pendent ethynyl groups

    NASA Technical Reports Server (NTRS)

    Hergenrother, P. M.; Jensen, B. J.; Havens, S. J.

    1984-01-01

    As part of an effort on tougher/solvent resistant matrix resins for composites, research was directed towards exploring methods to improve the solvent resistance of linear amorphous thermoplastics. Ethyl reactive groups were placed on the ends of oligomers and pendent along the polymer chain and subsequently thermally reacted to provide crosslinking and thus improvement in solvent resistance. This concept is extended to another thermoplastic, a phenoxy resin. A commercially available phenoxy resin (PKHH) was systematically modified by reaction of the pendent hydroxyl groups on the phenoxy resin with various amounts of 4-ethynylbenzoyl chloride. As the pendent ethynyl group content in the phenoxy resin increased, the cured resin exhibited a higher glass transition temperature, better solvent resistance and less flexibility. The solvent resistance was further improved by correcting a low molecular weight diethynyl compound, 2,2-bis(4-ethynylbenzoyloxy-4'-phenyl)propane, with a phenoxy resin containing pendent ethynyl groups.

  19. Foam, Foam-resin composite and method of making a foam-resin composite

    NASA Technical Reports Server (NTRS)

    Cranston, John A. (Inventor); MacArthur, Doug E. (Inventor)

    1995-01-01

    This invention relates to a foam, a foam-resin composite and a method of making foam-resin composites. The foam set forth in this invention comprises a urethane modified polyisocyanurate derived from an aromatic amino polyol and a polyether polyol. In addition to the polyisocyanurate foam, the composite of this invention further contains a resin layer, wherein the resin may be epoxy, bismaleimide, or phenolic resin. Such resins generally require cure or post-cure temperatures of at least 350.degree. F.

  20. High Temperature Transfer Molding Resins

    NASA Technical Reports Server (NTRS)

    Connell, John W. (Inventor); Smith, Joseph G., Jr. (Inventor); Hergenrother, Paul M. (Inventor)

    2000-01-01

    High temperature resins containing phenylethynyl groups that are processable by transfer molding have been prepared. These phenylethynyl containing oligomers were prepared from aromatic diamines containing phenylethynyl groups and various ratios of phthalic anhydride and 4-phenylethynlphthalic anhydride in glacial acetic acid to form a mixture of imide compounds in one step. This synthetic approach is advantageous since the products are a mixture of compounds and consequently exhibit a relatively low melting temperature. In addition, these materials exhibit low melt viscosities which are stable for several hours at 210-275 C, and since the thermal reaction of the phenylethynyl group does not occur to any appreciable extent at temperatures below 300 C, these materials have a broad processing window. Upon thermal cure at approximately 300-350 C, the phenylethynyl groups react to provide a crosslinked resin system. These new materials exhibit excellent properties and are potentially useful as adhesives, coatings, films, moldings and composite matrices.

  1. Advanced thermoplastic resins, phase 2

    NASA Technical Reports Server (NTRS)

    Brown, A. M.; Hill, S. G.; Falcone, A.

    1991-01-01

    High temperature structural resins are required for use on advanced aerospace vehicles as adhesives and composite matrices. NASA-Langley developed polyimide resins were evaluated as high temperature structural adhesives for metal to metal bonding and as composite matrices. Adhesive tapes were prepared on glass scrim fabric from solutions of polyamide acids of the semicrystalline polyimide LARC-CPI, developed at the NASA-Langley Research Center. Using 6Al-4V titanium adherends, high lap shear bond strengths were obtained at ambient temperature (45.2 MPa, 6550 psi) and acceptable strengths were obtained at elevated temperature (14.0 MPa, 2030 psi) using the Pasa-Jell 107 conversion coating on the titanium and a bonding pressure of 1.38 MPa (200 psi). Average zero degree composite tensile and compressive strengths of 1290 MPa (187 ksi) and 883 MPa (128 ksi) respectively were obtained at ambient temperature with unsized AS-4 carbon fiber reinforcement.

  2. Pharmaceutical Applications of Ion-Exchange Resins

    NASA Astrophysics Data System (ADS)

    Elder, David P.

    2005-04-01

    The historical uses of ion-exchange resins and a summary of the basic chemical principles involved in the ion-exchange process are discussed. Specific applications of ion-exchange resins are provided. The utility of these agents to stabilize drugs are evaluated. Commonly occurring chemical and physical incompatibilities are reviewed. Ion-exchange resins have found applicability as inactive pharmaceutical constituents, particularly as disintegrants (inactive tablet ingredient whose function is to rapidly disrupt the tablet matrix on contact with gastric fluid). One of the more elegant approaches to improving palatability of ionizable drugs is the use of ion-exchange resins as taste-masking agents. The selection, optimization of drug:resin ratio and particle size, together with a review of scaleup of typical manufacturing processes for taste-masked products are provided. Ion-exchange resins have been extensively utilized in oral sustained-release products. The selection, optimization of drug:resin ratio and particle size, together with a summary of commonly occurring commercial sustained-release products are discussed. Ion-exchange resins have also been used in topical products for local application to the skin, including those where drug flux is controlled by a differential electrical current (ionotophoretic delivery). General applicability of ion-exchange resins, including ophthalmic delivery, nasal delivery, use as drugs in their own right (e.g., colestyramine, formerly referred to as cholestyramine), as well as measuring gastrointestinal transit times, are discussed. Finally, pharmaceutical monographs for ion-exchange resins are reviewed.

  3. Phosphorus-containing imide resins

    NASA Technical Reports Server (NTRS)

    Varma, I. K.; Fohlen, G. M.; Parker, J. A. (Inventor)

    1984-01-01

    Flame-resistant reinforced bodies are disclosed which are composed of reinforcing fibers, filaments or fabrics in a cured body of bis- and tris-imide resins derived from tris(m-aminophenyl) phosphine oxides by reaction with maleic anhydride or its derivatives, or of addition polymers of such imides, including a variant in which a mono-imide is condensed with a dianhydride and the product is treated with a further quantity of maleic anhydride.

  4. High-Temperature Polyimide Resin

    NASA Technical Reports Server (NTRS)

    Vanucci, Raymond D.; Malarik, Diane C.

    1990-01-01

    Improved polyimide resin used at continuous temperatures up to 700 degrees F (371 degrees C). PMR-II-50, serves as matrix for fiber-reinforced composites. Material combines thermo-oxidative stability with autoclave processability. Used in such turbine engine components as air-bypass ducts, vanes, bearings, and nozzle flaps. Other potential applications include wing and fuselage skins on high-mach-number aircraft and automotive engine blocks and pistons.

  5. ELUTION OF URANIUM FROM RESIN

    DOEpatents

    McLEan, D.C.

    1959-03-10

    A method is described for eluting uranium from anion exchange resins so as to decrease vanadium and iron contamination and permit recycle of the major portion of the eluats after recovery of the uranium. Diminution of vanadium and iron contamination of the major portion of the uranium is accomplished by treating the anion exchange resin, which is saturated with uranium complex by adsorption from a sulfuric acid leach liquor from an ore bearing uranium, vanadium and iron, with one column volume of eluant prepared by passing chlorine into ammonium hydroxide until the chloride content is about 1 N and the pH is about 1. The resin is then eluted with 8 to 9 column volumes of 0.9 N ammonium chloride--0.1 N hydrochloric acid solution. The eluants are collected separately and treated with ammonia to precipitate ammonium diuranate which is filtered therefrom. The uranium salt from the first eluant is contaminated with the major portion of ths vanadium and iron and is reworked, while the uranium recovered from the second eluant is relatively free of the undesirable vanadium and irons. The filtrate from the first eluant portion is discarded. The filtrate from the second eluant portion may be recycled after adding hydrochloric acid to increase the chloride ion concentration and adjust the pH to about 1.

  6. Synthesis of improved polyester resins

    NASA Technical Reports Server (NTRS)

    Mcleod, A. H.; Delano, C. B.

    1979-01-01

    Eighteen aromatic unsaturated polyester prepolymers prepared by a modified interfacial condensation technique were investigated for their solubility in vinyl monomers and ability to provide high char yield forming unsaturated polyester resins. The best resin system contained a polyester prepolymer of phthalic, fumaric and diphenic acids reacted with 2,7-naphthalene diol and 9,9-bis(4-hydroxyphenyl)fluorene. This prepolymer is very soluble in styrene, divinyl benzene, triallyl cyanurate, diallyl isophthalate and methylvinylpyridine. It provided anaerobic char yields as high as 41 percent at 800 C. The combination of good solubility and char yield represents a significant improvement over state-of-the-art unsaturated polyester resins. The majority of the other prepolymers had only low or no solubility in vinyl monomers. Graphite composites from this prepolymer with styrene were investigated. The cause for the observed low shear strengths of the composites was not determined, however 12-week aging of the composites at 82 C showed that essentially no changes in the composites had occurred.

  7. 21 CFR 177.2510 - Polyvinylidene fluoride resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyvinylidene fluoride resins. 177.2510 Section... Repeated Use § 177.2510 Polyvinylidene fluoride resins. Polyvinylidene fluoride resins may be safely used... fluoride resins consist of basic resins produced by the polymerization of vinylidene fluoride. (b)...

  8. Incorporation of zero valent iron nanoparticles in the matrix of cationic resin beads for the remediation of Cr(VI) contaminated waters.

    PubMed

    Toli, Aikaterini; Chalastara, Konstantina; Mystrioti, Christiana; Xenidis, Anthimos; Papassiopi, Nymphodora

    2016-07-01

    The objective of present study was to obtain the fixation of nano zero valent iron (nZVI) particles on a permeable matrix and evaluate the performance of this composite material for the removal of Cr(VI) from contaminated waters. The experiments were carried out using the cationic resin Dowex 50WX2 as porous support of the iron nanoparticles. The work was carried out in two phases. The first phase involved the fixation of nZVI on the resin matrix. The resin granules were initially mixed with a FeCl3 solution to obtain the adsorption of Fe(III). Then the Fe(III) loaded resin (RFe) was treated with polyphenol solutions to obtain the reduction of Fe(III) to the elemental state. Two polyphenol solutions were tested as reductants, i.e. green tea extract and gallic acid. Green tea was found to be inefficient, probably due to the relatively big size of the contained polyphenol molecules, but gallic acid molecules were able to reach adsorbed Fe(III) and reduce the cations to the elemental state. The second phase was focused on the investigation of Cr(VI) reduction kinetics using the nanoiron loaded resins (R-nFe). It was found that the reduction follows a kinetic law of first order with respect to Cr(VI) and to the embedded nanoiron. Compared to other similar products, this composite material was found to have comparable performance regarding reaction rates and higher degree of iron utilization. Namely the rate constant for the reduction of Cr(VI), in the presence of 1 mM nZVI, was equivalent to 1.4 h of half-life time at pH 3.2 and increased to 24 h at pH 8.5. The degree of iron utilization was as high as 0.8 mol of reduced Cr(VI) per mole of iron. It was also found that this composite material can be easily regenerated and reused for Cr(VI) reduction without significant loss of efficiency. PMID:27108046

  9. Scintillating 99Tc Selective Ion Exchange Resins

    SciTech Connect

    Mitchell Greenhalgh; Richard D. Tillotson

    2012-07-01

    Scintillating technetium (99Tc) selective ion exchange resins have been developed and evaluated for equilibrium capacities and detection efficiencies. These resins can be utilized for the in-situ concentration and detection of low levels of pertechnetate anions (99TcO4-) in natural waters. Three different polystyrene type resin support materials were impregnated with varying amounts of tricaprylmethylammonium chloride (Aliquat 336) extractant, several different scintillating fluors and wavelength shifters. The prepared resins were contacted batch-wise to equilibrium over a wide range of 99TcO4- concentrations in natural water. The measured capacities were used to develop Langmuir adsorption isotherms for each resin. 99Tc detection efficiencies were determined and up to 71.4 ± 2.6% was achieved with some resins. The results demonstrate that a low level detection limit for 99TcO4- in natural waters can be realized.

  10. Development of tough, moisture resistant laminating resins

    NASA Technical Reports Server (NTRS)

    Brand, R. A.; Harrison, E. S.

    1982-01-01

    Tough, moisture resistant laminating resins for employment with graphite fibers were developed. The new laminating resins exhibited cost, handleability and processing characteristics equivalent to 394K (250 F) curing epoxies. The laminating resins were based on bisphenol A dicyanate and monofunctional cyanates with hydrophobic substituents. These resins sorb only small quantities of moisture at equilibrium (0.5% or less) with minimal glass transition temperature depression and represent an improvement over epoxies which sorb around 2% moisture at equilibrium. Toughening was accomplished by the precipitation of small diameter particles of butadiene nitrile rubber throughout the resin matrix. The rubber domains act as microcrack termini and energy dissipation sites, allowing increased stress accommodation prior to catastrophic failure. A unique blend of amine terminated butadiene nitrile elastomer (MW 2,000) and a high nitrile content butadiene nitrile rubber yielded the desired resin morphology.

  11. New modified hydrocarbon resins; An alternative to styrenated terpene resins in hot melts

    SciTech Connect

    Carper, J.D. )

    1990-06-01

    This paper reports on the development of two hydrocarbon-based resin formulations that could be used with different thermoplastic block copolymers to formulate pressure-sensitive adhesives. Results are examined with one of these resins in formulations with styrene-isoprene-styrene (SIS) and styrene-butadiene (SB) compounds. The new modified hydrocarbon resin, with a softening point of 98{degrees} C, matches the adhesive performance of a terpene resin with a softening point of 105{degrees} C. The resin performs as well as the modified terpene in SIS-, SB-, and EVA-based adhesives. The new hydrocarbon resin is especially well suited for hot-melt adhesives. It exhibits low volatility, good color stability, and excellent melt viscosity stability. Since the new resin is based on petroleum hydrocarbon feedstocks, it should be available at moderate, stable prices. The other hydrocarbon resin, with a softening point of 85{degrees} C, produced comparable results.

  12. Resin selection criteria for tough composite structures

    NASA Technical Reports Server (NTRS)

    Chamis, C. C.; Smith, G. T.

    1983-01-01

    Resin selection criteria are derived using a structured methodology consisting of an upward integrated mechanistic theory and its inverse (top-down structured theory). These criteria are expressed in a "criteria selection space" which are used to identify resin bulk properties for improved composite "toughness". The resin selection criteria correlate with a variety of experimental data including laminate strength, elevated temperature effects and impact resistance.

  13. Porous Ceramic Spheres from Ion Exchange Resin

    NASA Technical Reports Server (NTRS)

    Dynys, Fred

    2005-01-01

    A commercial cation ion exchange resin, cross-linked polystyrene, has been successfully used as a template to fabricate 20 to 50 micron porous ceramic spheres. Ion exchange resins have dual template capabilities. Pore architecture of the ceramic spheres can be altered by changing the template pattern. Templating can be achieved by utilizing the internal porous structure or the external surface of the resin beads. Synthesis methods and chemical/physical characteristics of the ceramic spheres will be reported.

  14. Characterization of PMR polyimide resin and prepreg

    NASA Technical Reports Server (NTRS)

    Lindenmeyer, P. H.; Sheppard, C. H.

    1984-01-01

    Procedures for the chemical characterization of PMR-15 resin solutions and graphite-reinforced prepregs were developed, and a chemical data base was established. In addition, a basic understanding of PMR-15 resin chemistry was gained; this was translated into effective processing procedures for the production of high quality graphite composites. During the program the PMR monomers and selected model compounds representative of postulated PMR-15 solution chemistry were acquired and characterized. Based on these data, a baseline PMR-15 resin was formulated and evaluated for processing characteristics and composite properties. Commercially available PMR-15 resins were then obtained and chemically characterized. Composite panels were fabricated and evaluated.

  15. 21 CFR 177.1550 - Perfluorocarbon resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... for repeated use in contact with food. (d) Specifications—(1) Infrared identification. Perfluorocarbon resins can be identified by their characteristic infrared spectra. (2) Melt-viscosity. (i) The...

  16. Bending rigidity of composite resin coating clasps.

    PubMed

    Ikebe, K; Kibi, M; Ono, T; Nokubi, T

    1993-12-01

    The purpose of this study is to examine the bending profiles of composite resin coating cast clasps. The cobalt-chromium alloy cast clasps were made using tapered wax pattern. Silane coupling method (Silicoater MD, Kulzer Co.) was used to attach composite resin to metal surface. The breakage and the bending rigidity of composite resin coating clasps were evaluated. Results were as follows: 1) After the repeated bending test to the tips of clasp arm at 10,000 times in 0.25 mm deflection, neither crack on composite resin surface nor separation at resin/metal interface was observed in any specimen. 2) There was no significant difference in the bending rigidity of clasp arms between before and after composite resin coating. From these results, it was demonstrated that the composite resin coating cast clasp was available in clinical cases and coating with composite resin had little influence on the bending rigidity of clasp arms. Therefore, it was suggested that our clasp designing and fabricating system to control the bending rigidity of clasp arms could be applied to composite resin coating clasps. PMID:8935086

  17. Sand control with resin and explosive

    SciTech Connect

    Dees, J.M.; Begnaud, W.J.; Sahr, N.L.

    1992-09-08

    This patent describes a method for treating a well having perforated casing to prevent solids movement through the perforations and into the wellbore. It comprises positioning a quantity of liquid resin solution such that the solution occupies the interval of the casing having perforations; positioning an explosive in proximity with the liquid resin solution; detonating the explosive; displacing the liquid resin solution remaining in the wellbore after step (c) through the perforations with a displacing fluid; and injecting a chemical solution through the perforations to cause the resin to polymerize to form a consolidated permeable matrix.

  18. Novel silica-based ion exchange resin

    SciTech Connect

    1997-11-01

    Eichrom`s highly successful Diphonixo resin resembles a conventional ion exchange resin in its use of sulfonic acid ligands on a styrene- divinylbenzene matrix. Diphonix resin exhibits rapid exchange kinetics that allow economical operation of ion exchange systems. Unlike conventional resins, Diphonix resin contains chelating ligands that are diphosphonic acid groups that recognize and remove the targeted metals and reject the more common elements such as sodium, calcium and magnesium. This latter property makes Diphonix ideal for many industrial scale applications, including those involving waste treatment. For treatment of low-level, transuranic (TRU) and high- level radioactive wastes, Diphonix`s polystyrene backbone hinders its application due to radiolytic stability of the carbon-hydrogen bonds and lack of compatibility with expected vitrification schemes. Polystyrene-based Diphonix is approximately 60% carbon- hydrogen. In response to an identified need within the Department of Energy for a resin with the positive attributes of Diphonix that also exhibits greater radiolytic stability and final waste form compatibility, Eichrom has successfully developed a new, silica-based resin version of Diphonix. Target application for this new resin is for use in environmental restoration and waste management situations involving the processing of low-level, transuranic and high-level radioactive wastes. The resin can also be used for processing liquid mixed waste (waste that contains low level radioactivity and hazardous constituents) including mixed wastes contaminated with organic compounds. Silica-based Diphonix is only 10% carbon-hydrogen, with the bulk of the matrix silica.

  19. Imide modified epoxy matrix resins

    NASA Technical Reports Server (NTRS)

    Scola, D. A.

    1982-01-01

    Results of a program designed to develop tough imide modified epoxy (IME) resins cured by bisimide amine (BIA) hardeners are presented. State of the art epoxy resin, MY720, was used. Three aromatic bisimide amines and one aromatic aliphatic BIA were evaluated. BIA's derived from 6F anhydride (3,3 prime 4,4 prime-(hexafluoro isopropyl idene) bis (phthalic anhydride) and diamines, 3,3 prime-diam nodiphenyl sulfone (3,3 prime-DDS), 4,4 prime-diamino diphenyl sulfone (4,4 prime-DDS), 1.12-dodecane diamine (1,12-DDA) were used. BIA's were abbreviated 6F-3,3 prime-DDS, 6F-4,4 prime-DDS, 6F-3,3 prime-DDS-4,4 prime DDS, and 6F-3,3 prime-DDS-1,12-DDA corresponding to 6F anhydride and diamines mentioned. Epoxy resin and BIA's (MY720/6F-3,3 prime-DDS, MY720/6F-3,3 prime-DDS-4,4 prime-DDS, MY720/6F-3,3 prime-DDS-1,12-DDA and a 50:50 mixture of a BIA and parent diamine, MY720/6F-3,3 prime-DDS/3,3 prime-DDS, MY720/6F-3,3 prime-DDS-4,4 prime-DDS/3,3 prime-DDS, MY720/6F-3,3 prime-DDS-1,12-DDA/3,3 prime-DDS were studied to determine effect of structure and composition. Effect of the addition of two commercial epoxies, glyamine 200 and glyamine 100 on the properties of several formulations was evaluated. Bisimide amine cured epoxies were designated IME's (imide modified epoxy). Physical, thermal and mechanical properties of these resins were determined. Moisture absorption in boiling water exhibited by several of the IME's was considerably lower than the state of the art epoxies (from 3.2% for the control and state of the art to 2.0 wt% moisture absorption). Char yields are increased from 20% for control and state of the art epoxies to 40% for IME resins. Relative toughness characteristics of IME resins were measured by 10 deg off axis tensile tests of Celion 6000/IME composites. Results show that IME's containing 6F-3,3 prime-DDS or 6F-3,3 prime-DDS-1,12-DDA improved the "toughness" characteristics of composites by about 35% (tensile strength), about 35% (intralaminar shear

  20. High refractive index photocurable resins

    NASA Astrophysics Data System (ADS)

    Morford, Robert V.; Mercado, Ramil L.; Planje, Curtis E.; Flaim, Tony D.

    2005-04-01

    The performance of optoelectronic devices can be increased by incorporating a high refractive index layer into the system. This paper describes several potential high refractive index resin candidates. Our materials include the added advantages over other systems because the new materials are cationically photocurable and free flowing, have low shrinkage upon cure, have no (or little) volatile organic components, are applicable by a variety of methods (dip coating, roller coating, injection molding, or film casting), can be applied in a variety of thicknesses (10-100 m), are fast-curing, and possess robust physical properties. Particular attention focuses on the refractive index in the visible spectrum, light transmission, and formulation viscosity.

  1. Polyimide Resins Resist Extreme Temperatures

    NASA Technical Reports Server (NTRS)

    2009-01-01

    Spacecraft and aerospace engines share a common threat: high temperature. The temperatures experienced during atmospheric reentry can reach over 2,000 F, and the temperatures in rocket engines can reach well over 5,000 F. To combat the high temperatures in aerospace applications, Dr. Ruth Pater of Langley Research Center developed RP-46, a polyimide resin capable of withstanding the most brutal temperatures. The composite material can push the service temperature to the limits of organic materials. Designed as an environmentally friendly alternative to other high-temperature resins, the RP-46 polyimide resin system was awarded a 1992 "R&D 100" award, named a "2001 NASA Technology of the Year," and later, due to its success as a spinoff technology, "2004 NASA Commercial Invention of the Year." The technology s commercial success also led to its winning the Langley s "Paul F. Holloway Technology Transfer Award" as well as "Richard T. Whitcom Aerospace Technology Transfer Award" both for 2004. RP-46 is relatively inexpensive and it can be readily processed for use as an adhesive, composite, resin molding, coating, foam, or film. Its composite materials can be used in temperatures ranging from minus 150 F to 2,300 F. No other organic materials are known to be capable of such wide range and extreme high-temperature applications. In addition to answering the call for environmentally conscious high-temperature materials, RP-46 provides a slew of additional advantages: It is extremely lightweight (less than half the weight of aluminum), chemical and moisture resistant, strong, and flexible. Pater also developed a similar technology, RP-50, using many of the same methods she used with RP-46, and very similar in composition to RP-46 in terms of its thermal capacity and chemical construction, but it has different applications, as this material is a coating as opposed to a buildable composite. A NASA license for use of this material outside of the Space Agency as well as

  2. Phosphorus-containing imide resins

    NASA Technical Reports Server (NTRS)

    Varma, I. K.; Fohlen, G. M.; Parker, J. A. (Inventor)

    1985-01-01

    Cured polymers of bis and tris-imides derived from tris(m-aminophenyl) phosphine oxides by reaction with maleic anhydride or its derivatives, and addition polymers of such imides, including a variant in which a monoimide is condensed with a dianhydride and the product is treated with a further quantity of maleic anhydride prior to curing are disclosed and claimed. Such polymers are flame resistant. Also disclosed are an improved method of producing tris(m-aminophenyl) phosphine oxides from the nitro analogues by reduction with hydrazine hydrate using palladized charcoal or Raney nickel as the catalyst and fiber reinforced cured resin composites.

  3. 21 CFR 175.380 - Xylene-formaldehyde resins condensed with 4,4′-isopropylidenediphenol-epichlorohydrin epoxy resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... condensation of xylene-formaldehyde resin and 4,4′-isopropylidenediphenol-epichlorohydrin epoxy resins, to... include resins produced by the condensation of allyl ether of mono-, di-, or trimethylol phenol and...

  4. Silicone modified resins for graphite fiber laminates

    NASA Technical Reports Server (NTRS)

    Frost, L. W.; Bower, G. M.

    1980-01-01

    Six silicone modified resins were selected for evaluation in unidirectional filament wound graphite laminates. Neat samples of these resins had 1,000 C char residues of 6-63%. The highest flexural values measured for the laminates were a strength of 1,220 MPa and a modulus of 105 GPa. The highest interlaminar shear strength was 72 MPa.

  5. Some experiences with epoxy resin grouting compounds.

    PubMed

    Hosein, H R

    1980-07-01

    Epoxy resin systems are used in tiling and grouting in the construction industry. Because of the nature of the application, skin contact is the primary hazard. The most prevalent reaction was reddening of the forearms, followed by whole body reddening and loss of appetite, these latter two being associated with smoking while applying the resin. PMID:7415974

  6. Fluorinated diamond bonded in fluorocarbon resin

    DOEpatents

    Taylor, Gene W.

    1982-01-01

    By fluorinating diamond grit, the grit may be readily bonded into a fluorocarbon resin matrix. The matrix is formed by simple hot pressing techniques. Diamond grinding wheels may advantageously be manufactured using such a matrix. Teflon fluorocarbon resins are particularly well suited for using in forming the matrix.

  7. Modified resins for solid-phase extraction

    DOEpatents

    Fritz, James S.; Sun, Jeffrey J.

    1993-07-27

    A process of treating aqueous solutions to remove organic solute contaminants by contacting an aqueous solution containing polar organic solute contaminants with a functionalized polystyrene-divinyl benzene adsorbent resin, with the functionalization of said resin being accomplished by organic hydrophilic groups such as hydroxymethyl, acetyl and cyanomethyl.

  8. Modified resins for solid-phase extraction

    DOEpatents

    Fritz, James S.; Sun, Jeffrey J.

    1991-12-10

    A process of treating aqueous solutions to remove organic solute contaminants by contacting an aqueous solution containing polar organic solute contaminants with a functionalized polystyrene-divinyl benzene adsorbent resin, with the functionalization of said resin being accomplished by organic hydrophilic groups such as hydroxymethyl, acetyl and cyanomethyl.

  9. 21 CFR 177.1555 - Polyarylate resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1555 Polyarylate resins. Polyarylate resins (CAS Reg. No. 51706-10-6) may be safely used as articles or components of articles intended for use...

  10. 21 CFR 177.1555 - Polyarylate resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1555 Polyarylate resins. Polyarylate resins (CAS Reg. No. 51706-10-6) may be safely used as articles or components of articles intended for use...

  11. 21 CFR 177.1555 - Polyarylate resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1555 Polyarylate resins. Polyarylate resins (CAS Reg. No. 51706-10-6) may be safely used as articles or components of articles intended for use...

  12. TMI-2 purification demineralizer resin study

    SciTech Connect

    Thompson, J D; Osterhoudt, T R

    1984-05-01

    Study of the Makeup and Purification System demineralizers at TMI-2 has established that fuel quantities in the vessels are low, precluding criticality, that the high radioactive cesium concentration on the demineralizer resins can be chemically removed, and that the demineralizer resins can probably be removed from the vessels by sluicing through existing plant piping. Radiation measurements from outside the demineralizers establishing that there is between 1.5 and 5.1 (probably 3.3) lb of fuel in the A vessel and less than that amount in the B vessel. Dose rates up to 2780 R per hour were measured on contact with the A demineralizer. Remote visual observation of the A demineralizer showed a crystalline crust overlaying amber-colored resins. The cesium activity in solid resin samples ranged from 220 to 16,900 ..mu..Ci/g. Based on this information, researchers concluded that the resins cannot be removed through the normal pathway in their present condition. Studies do show that the resins will withstand chemical processing designed to rinse and elute cesium from the resins. The process developed should work on the TMI-2 resins.

  13. Effect of Resin Viscosity in Fiber Reinforcement Compaction in Resin Injection Pultrusion Process

    NASA Astrophysics Data System (ADS)

    Shakya, N.; Roux, J. A.; Jeswani, A. L.

    2013-12-01

    In resin injection pultrusion, the liquid resin is injected through the injection slots into the fiber reinforcement; the liquid resin penetrates through the fibers as well as pushes the fibers towards the centerplane causing fiber compaction. The compacted fibers are more difficult to penetrate, thus higher resin injection pressure becomes necessary to achieve complete reinforcement wetout. Lower injection pressures below a certain range (depending upon the fiber volume fraction and resin viscosity) cannot effectively penetrate through the fiber bed and thus cannot achieve complete wetout. Also, if the degree of compaction is very high the fibers might become essentially impenetrable. The more viscous the resin is, the harder it is to penetrate through the fibers and vice versa. The effect of resin viscosity on complete wetout achievement with reference to fiber-reinforcement compaction is presented in this study.

  14. Optical and color stabilities of paint-on resins for shade modification of restorative resins.

    PubMed

    Arikawa, Hiroyuki; Kanie, Takahito; Fujii, Koichi; Ban, Seiji; Homma, Tetsuya; Takahashi, Hideo

    2004-06-01

    The purpose of this study was to examine the optical and color stabilities of the paint-on resin used for shade modification of restorative resins. Three shades of paint-on resin and two crown and bridge resins were used. The light transmittance characteristics of the materials during accelerated aging tests such as water immersion, toothbrush abrasion, ultraviolet (UV) light irradiation, and staining tests were measured. Discolorations of materials resulting from tests were also determined. There were no significant effects of water immersion, toothbrush abrasion and UV light irradiation on the light transmittance and visible color change of paint-on resins, whereas the staining tests significantly decreased the light transmittance and increased color change of the translucent shades of materials. Our results indicate that the paint-on resins exhibit stable optical properties and color appearance, which are at least as good as the crown and bridge resins. PMID:15287561

  15. Resin/graphite fiber composites

    NASA Technical Reports Server (NTRS)

    Cavano, P. J.

    1974-01-01

    Techniques were developed that provided thermo-oxidatively stable A-type polyimide/graphite fiber composites using the approach of in situ polymerization of monomeric reactants directly on reinforcing fibers, rather than employing separately prepared prepolymer varnish. This was accomplished by simply mixing methylene dianiline and two ester-acids and applying this solution to the fibers for subsequent molding. Five different formulated molecular weight resins were examined, and an optimized die molding procedure established for the 1500 formulated molecular weight system. Extensive ultrasonic inspection of composites was successfully utilized as a technique for monitoring laminate quality. Composite mechanical property studies were conducted with this polyimide resin at room temperature and after various time exposures in a thermo-oxidative environment at 561 K (550 F), 589 K (600 F) and 617 K (650 F). It was determined that such composites have a long term life in the temperature range of 561 K to 589 K. The final phase involved the fabrication and evaluation of a series of demonstration airfoil specimens.

  16. Evaluation of resins for provisional restorations.

    PubMed

    Burgess, J O; Haveman, C W; Butzin, C

    1992-06-01

    An in vivo study of two resin materials (Barricaid and Caulk Temporary Crown and Bridge Resin) was done to determine the retention, post-operative sensitivity, and fabrication time of provisional restorations made from these materials. Following the placement of these resins in 67 intracoronal cavity preparations of 19 adult patients, a baseline evaluation was made which included a clinical examination and color slides. Twenty-four hours after the temporary restorations were placed, the patients completed evaluations of the post-operative sensitivity experienced. There was no difference in post-operative sensitivity between the teeth restored with Barricaid or Caulk Temporary Crown and Bridge Resin. At the insertion appointment of the final restoration, the interim restoration's success rate was determined. There was no difference between the retention of the two provisional materials. Fabrication time was significantly different with Barricaid restorations requiring less than one-half the fabrication time of the Caulk Temporary Crown and Bridge Resin material. PMID:1388950

  17. Release and toxicity of dental resin composite

    PubMed Central

    Gupta, Saurabh K.; Saxena, Payal; Pant, Vandana A.; Pant, Aditya B.

    2012-01-01

    Dental resin composite that are tooth-colored materials have been considered as possible substitutes to mercury-containing silver amalgam filling. Despite the fact that dental resin composites have improved their physico-chemical properties, the concern for its intrinsic toxicity remains high. Some components of restorative composite resins are released in the oral environment initially during polymerization reaction and later due to degradation of the material. In vitro and in vivo studies have clearly identified that these components of restorative composite resins are toxic. But there is a large gap between the results published by research laboratories and clinical reports. The objective of this manuscript was to review the literature on release phenomenon as well as in vitro and in vivo toxicity of dental resin composite. Interpretation made from the recent data was also outlined. PMID:23293458

  18. Physical Properties of Synthetic Resin Materials

    NASA Technical Reports Server (NTRS)

    Fishbein, Meyer

    1939-01-01

    A study was made to determine the physical properties of synthetic resins having paper, canvas, and linen reinforcements, and of laminated wood impregnated with a resin varnish. The results show that commercial resins have moduli of elasticity that are too low for structural considerations. Nevertheless, there do exist plastics that have favorable mechanical properties and, with further development, it should be possible to produce resin products that compare favorably with the light-metal alloys. The results obtained from tests on Compound 1840, resin-impregnated wood, show that this material can stand on its own merit by virtue of a compressive strength four times that of the natural wood. This increase in compressive strength was accomplished with an increase of density to a value slightly below three times the normal value and corrected one of the most serious defects of the natural product.

  19. Solidification of ion exchange resin wastes

    SciTech Connect

    Not Available

    1982-08-01

    Solidification media investigated included portland type I, portland type III and high alumina cements, a proprietary gypsum-based polymer modified cement, and a vinyl ester-styrene thermosetting plastic. Samples formulated with hydraulic cement were analyzed to investigate the effects of resin type, resin loading, waste-to-cement ratio, and water-to-cement ratio. The solidification of cation resin wastes with portland cement was characterized by excessive swelling and cracking of waste forms, both after curing and during immersion testing. Mixed bed resin waste formulations were limited by their cation component. Additives to improve the mechanical properties of portland cement-ion exchange resin waste forms were evaluated. High alumina cement formulations dislayed a resistance to deterioration of mechanical integrity during immersion testing, thus providing a significant advantage over portland cements for the solidification of resin wastes. Properties of cement-ion exchange resin waste forms were examined. An experiment was conducted to study the leachability of /sup 137/Cs, /sup 85/Sr, and /sup 60/Co from resins modified in portland type III and high alumina cements. The cumulative /sup 137/Cs fraction release was at least an order of magnitude greater than that of either /sup 85/Sr or /sup 60/Co. Release rates of /sup 137/Cs in high alumina cement were greater than those in portland III cement by a factor of two.Compressive strength and leach testing were conducted for resin wastes solidified with polymer-modified gypsum based cement. /sup 137/Cs, /sup 85/Sr, and /sup 60/Co fraction releases were about one, two and three orders of magnitude higher, respectively, than in equivalent portland type III cement formulations. As much as 28.6 wt % dry ion exchange resin was successfully solidified using vinyl ester-styrene compared with a maximum of 25 wt % in both portland and gypsum-based cement.

  20. Resin/graphite fiber composites

    NASA Technical Reports Server (NTRS)

    Cavano, P. J.

    1974-01-01

    Processing techniques were developed for the fabrication of both polyphenylquinoxaline and polyimide composites by the in situ polymerization of monomeric reactants directly on the graphite reinforcing fibers, rather than using previously prepared prepolymer varnishes. Void-free polyphenylquinoxaline composites were fabricated and evaluated for room and elevated flexure and shear properties. The technology of the polyimide system was advanced to the point where the material is ready for commercial exploitation. A reproducible processing cycle free of operator judgment factors was developed for fabrication of void-free composites exhibiting excellent mechanical properties and a long time isothermal life in the range of 288 C to 316 C. The effects of monomer reactant stoichiometry and process modification on resin flow were investigated. Demonstration of the utility and quality of this polyimide system was provided through the successful fabrication and evaluation of four complex high tip speed fan blades.

  1. 49 CFR 173.165 - Polyester resin kits.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 49 Transportation 2 2014-10-01 2014-10-01 false Polyester resin kits. 173.165 Section 173.165... Polyester resin kits. (a) Polyester resin kits consisting of a base material component (Class 3, Packing..., according to the criteria for Class 3, applied to the base material. Additionally, polyester resin kits...

  2. 49 CFR 173.165 - Polyester resin kits.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 49 Transportation 2 2013-10-01 2013-10-01 false Polyester resin kits. 173.165 Section 173.165... Polyester resin kits. (a) Polyester resin kits consisting of a base material component (Class 3, Packing..., according to the criteria for Class 3, applied to the base material. Additionally, polyester resin kits...

  3. 49 CFR 173.165 - Polyester resin kits.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 49 Transportation 2 2012-10-01 2012-10-01 false Polyester resin kits. 173.165 Section 173.165... Polyester resin kits. (a) Except for transportation by aircraft, polyester resin kits consisting of a base.... Additionally, unless otherwise excepted in this subchapter, polyester resin kits must be packaged...

  4. 21 CFR 176.110 - Acrylamide-acrylic acid resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Acrylamide-acrylic acid resins. 176.110 Section... Paper and Paperboard § 176.110 Acrylamide-acrylic acid resins. Acrylamide-acrylic acid resins may be...) Acrylamide-acrylic acid resins are produced by the polymerization of acrylamide with partial hydrolysis or...

  5. 21 CFR 177.2355 - Mineral reinforced nylon resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Mineral reinforced nylon resins. 177.2355 Section... Repeated Use § 177.2355 Mineral reinforced nylon resins. Mineral reinforced nylon resins identified in... reinforced nylon resins consist of nylon 66, as identified in and complying with the specifications of §...

  6. Properties of a nanodielectric cryogenic resin

    SciTech Connect

    Polyzos, Georgios; Tuncer, Enis; Sauers, Isidor; More, Karren Leslie

    2010-01-01

    Physical properties of a nanodielectric composed of in situ synthesized titanium dioxide (TiO{sub 2}) nanoparticles ({le} 5 nm in diameter) and a cryogenic resin are reported. The dielectric losses were reduced by a factor of 2 in the nanocomposite, indicating that the presence of small TiO{sub 2} nanoparticles restricted the mobility of the polymer chains. Dielectric breakdown data of the nanodielectric was distributed over a narrower range than that of the unfilled resin. The nanodielectric had 1.56 times higher 1% breakdown probability than the resin, yielding 0.64 times thinner insulation thickness for the same voltage level, which is beneficial in high voltage engineering.

  7. Class II Resin Composites: Restorative Options.

    PubMed

    Patel, Minesh; Mehta, Shamir B; Banerji, Subir

    2015-10-01

    Tooth-coloured, resin composite restorations are amongst the most frequently prescribed forms of dental restoration to manage defects in posterior teeth. The attainment of a desirable outcome when placing posterior resin composite restorations requires the clinician to have a good understanding of the benefits (as well as the limitations) posed by this material, together with a sound knowledge of placement technique. Numerous protocols and materials have evolved to assist the dental operator with this type of demanding posterior restoration. With the use of case examples, four techniques available are reported here. CPD/Clinical Relevance: This article explores varying techniques for the restoration of Class II cavities using resin composite. PMID:26685471

  8. Improved microbial-check-valve resins

    NASA Technical Reports Server (NTRS)

    Colombo, G. V.; Putnam, D. F.

    1980-01-01

    Improved microbial-check-valve resins have been tested for their microbicidal effectiveness and long-term stability. Resins give more-stable iodine concentrations than previous preparations and do not impart objectionable odor or taste to treated water. Microbial check valve is small cylindrical device, packed with iodide-saturated resin, that is installed in water line where contamination by micro-organisms is to be prevented. Prototype microbial check valve was tested for stability and performance under harsh environmental conditions. Effectiveness was 100 percent at 35 deg, 70 deg, and 160 deg F (2 deg, 21 deg, and 71 deg C).

  9. Chemical Characterization of Phenol/Formaldehyde Resins

    NASA Technical Reports Server (NTRS)

    Brayden, T. H.

    1986-01-01

    Report discusses tests of commercial phenol/formaldehyde resins to establish relationships among composition before use, behavior during curing, and strength after curing. Resin used in carbon/carbon laminates. In curing process, two molecules of phenol joined together in sequence of reactions involving molecule of formaldehyde. Last step of sequence, molecule of water released. Sequence repeats until one of ingredients used up, leaving solidified thermoset plastic. Issues to be resolved: number and relative abundances of ingredients, presence of certain chemical groups, heat-producing ability of resin, and range of molecular weights present.

  10. SEM and elemental analysis of composite resins

    SciTech Connect

    Hosoda, H.; Yamada, T.; Inokoshi, S. )

    1990-12-01

    Twenty-four chemically cured, 21 light-cured anterior, three light-cured anterior/posterior, and 18 light-cured posterior composite resins were examined using scanning electron microscopy, and the elemental composition of their filler particles was analyzed with an energy dispersive electron probe microanalyzer. According to the results obtained, the composite resins were divided into five groups (traditional, microfilled type, submicrofilled type, hybrid type, and semihybrid), with two additional hypothetical categories (microfilled and hybrid). Characteristics of each type were described with clinical indications for selective guidance of respective composite resins for clinical use.

  11. Cobalt Ions Improve the Strength of Epoxy Resins

    NASA Technical Reports Server (NTRS)

    Stoakley, D. M.; St. Clair, A. K.

    1986-01-01

    Technique developed for improving mechanical strength of epoxy resins by adding cobalt ions in form of tris(acetylacetonato)cobalt (III) complex. Solid cast disks prepared from cobalt ion-containing epoxy resins tested for flexural strength and stiffness. Incorporation of cobalt ions into epoxies increased flexural strength of resins by 10 to 95 percent. Suitable resins for this technique include any liquid or solid TGMDA resins. Improved epoxy formulation proves useful as composite matrix resin, adhesive, or casting resin for applications on commercial and advanced aircraft.

  12. Hydraulic Permeability of Resorcinol-Formaldehyde Resin

    SciTech Connect

    Taylor, Paul Allen

    2010-01-01

    An ion exchange process using spherical resorcinol-formaldehyde (RF) resin is the baseline process for removing cesium from the dissolved salt solution in the high-level waste tanks at the Hanford Site, using large scale columns as part of the Waste Treatment Plant (WTP). The RF resin is also being evaluated for use in the proposed small column ion exchange (SCIX) system, which is an alternative treatment option at Hanford and at the Savannah River Site (SRS). A recirculating test loop with a small ion exchange column was used to measure the effect of oxygen uptake and radiation exposure on the permeability of a packed bed of the RF resin. The lab-scale column was designed to be prototypic of the proposed Hanford columns at the WTP. Although the test equipment was designed to model the Hanford ion exchange columns, the data on changes in the hydraulic permeability of the resin will also be valuable for determining potential pressure drops through the proposed SCIX system. The superficial fluid velocity in the lab-scale test (3.4-5.7 cm/s) was much higher than is planned for the full-scale Hanford columns to generate the maximum pressure drop expected in those columns (9.7 psig). The frictional drag from this high velocity produced forces on the resin in the lab-scale tests that matched the design basis of the full-scale Hanford column. Any changes in the resin caused by the radiation exposure and oxygen uptake were monitored by measuring the pressure drop through the lab-scale column and the physical properties of the resin. Three hydraulic test runs were completed, the first using fresh RF resin at 25 C, the second using irradiated resin at 25 C, and the third using irradiated resin at 45 C. A Hanford AP-101 simulant solution was recirculated through a test column containing 500 mL of Na-form RF resin. Known amounts of oxygen were introduced into the primary recirculation loop by saturating measured volumes of the simulant solution with oxygen and reintroducing

  13. Dental repair material: a resin-modified glass-ionomer bioactive ionic resin-based composite.

    PubMed

    Croll, Theodore P; Berg, Joel H; Donly, Kevin J

    2015-01-01

    This report documents treatment and repair of three carious teeth that were restored with a new dental repair material that features the characteristics of both resin-modified glass-ionomer restorative cement (RMGI) and resin-based composite (RBC). The restorative products presented are reported by the manufacturer to be the first bioactive dental materials with an ionic resin matrix, a shock-absorbing resin component, and bioactive fillers that mimic the physical and chemical properties of natural teeth. The restorative material and base/liner, which feature three hardening mechanisms, could prove to be a notable advancement in the adhesive dentistry restorative materials continuum. PMID:25822408

  14. Phenoxy resins containing pendent ethynyl groups and cured resins obtained therefrom

    NASA Technical Reports Server (NTRS)

    Hergenrother, P. M. (Inventor)

    1985-01-01

    Phenoxy resins containing pendent ethynyl groups, the process for preparing the same, and the cured resin products obtained therefrom are disclosed. Upon the application of heat, the ethynyl groups react to provide branching and crosslinking with the cure temperature being lowered by using a catalyst if desired but not required. The cured phenoxy resins containing pendent ethynyl groups have improved solvent resistance and higher use temperature than linear uncrosslinked phenoxy resins and are applicable for use as coatings, films, adhesives, composited matrices and molding compounds.

  15. Method for regenerating magnetic polyamine-epichlorohydrin resin

    DOEpatents

    Kochen, Robert L.; Navratil, James D.

    1997-07-29

    Magnetic polymer resins capable of efficient removal of actinides and heavy metals from contaminated water are disclosed together with methods for making, using, and regenerating them. The resins comprise polyamine-epichlorohydrin resin beads with ferrites attached to the surfaces of the beads. Markedly improved water decontamination is demonstrated using these magnetic polymer resins of the invention in the presence of a magnetic field, as compared with water decontamination methods employing ordinary ion exchange resins or ferrites taken separately.

  16. Method for regenerating magnetic polyamine-epichlorohydrin resin

    DOEpatents

    Kochen, R.L.; Navratil, J.D.

    1997-07-29

    Magnetic polymer resins capable of efficient removal of actinides and heavy metals from contaminated water are disclosed together with methods for making, using, and regenerating them. The resins comprise polyamine-epichlorohydrin resin beads with ferrites attached to the surfaces of the beads. Markedly improved water decontamination is demonstrated using these magnetic polymer resins of the invention in the presence of a magnetic field, as compared with water decontamination methods employing ordinary ion exchange resins or ferrites taken separately. 9 figs.

  17. 21 CFR 177.1550 - Perfluorocarbon resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... articles intended for repeated use in contact with food. (d) Specifications—(1) Infrared identification. Perfluorocarbon resins can be identified by their characteristic infrared spectra. (2) Melt-viscosity. (i) The...

  18. Determining resin/fiber content of laminates

    NASA Technical Reports Server (NTRS)

    Garrard, G. G.; Houston, D. W.

    1979-01-01

    Article discusses procedure where hydrazine is used to extract graphite fibers from cured polyimide resin. Method does not attack graphite fibers and is faster than hot-concentrated-acid digestion process.

  19. Silicone modified resins for graphite fiber laminates

    NASA Technical Reports Server (NTRS)

    Frost, L. W.; Bower, G. M.

    1979-01-01

    The development of silicon modified resins for graphite fiber laminates which will prevent the dispersal of graphite fibers when the composites are burned is discussed. Eighty-five silicone modified resins were synthesized and evaluated including unsaturated polyesters, thermosetting methacrylates, epoxies, polyimides, and phenolics. Neat resins were judged in terms of Si content, homogeneity, hardness, Char formation, and thermal stability. Char formation was estimated by thermogravimetry to 1,000 C in air and in N2. Thermal stability was evaluated by isothermal weight loss measurements for 200 hrs in air at three temperatures. Four silicone modified epoxies were selected for evaluation in unidirectional filament wound graphite laminates. Neat samples of these resins had 1,000 C char residues of 25 to 50%. The highest flexural values measured for the laminates were a strength of 140 kpsi and a modulus of 10 Mpsi. The highest interlaminar shear strength was 5.3 kpsi.

  20. Synthesis of improved phenolic and polyester resins

    NASA Technical Reports Server (NTRS)

    Delano, C. B.

    1980-01-01

    Thirty-seven cured phenolic resin compositions were prepared and tested for their ability to provide improved char residues and moisture resistance over state of the art epoxy resin composite matrices. Cyanate, epoxy novolac and vinyl ester resins were investigated. Char promoter additives were found to increase the anaerobic char yield at 800 C of epoxy novolacs and vinyl esters. Moisture resistant cyanate and vinyl ester compositions were investigated as composite matrices with Thornel 300 graphite fiber. A cyanate composite matrix provided state of the art composite mechanical properties before and after humidity exposure and an anaerobic char yield of 46 percent at 800 C. The outstanding moisture resistance of the matrix was not completely realized in the composite. Vinyl ester resins showed promise as candidates for improved composite matrix systems.

  1. 21 CFR 872.3140 - Resin applicator.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... applicator is a brushlike device intended for use in spreading dental resin on a tooth during application of tooth shade material. (b) Classification. Class I (general controls). The device is exempt from...

  2. 21 CFR 872.3140 - Resin applicator.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... applicator is a brushlike device intended for use in spreading dental resin on a tooth during application of tooth shade material. (b) Classification. Class I (general controls). The device is exempt from...

  3. 21 CFR 872.3140 - Resin applicator.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... applicator is a brushlike device intended for use in spreading dental resin on a tooth during application of tooth shade material. (b) Classification. Class I (general controls). The device is exempt from...

  4. 21 CFR 872.3140 - Resin applicator.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... applicator is a brushlike device intended for use in spreading dental resin on a tooth during application of tooth shade material. (b) Classification. Class I (general controls). The device is exempt from...

  5. 21 CFR 872.3140 - Resin applicator.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... applicator is a brushlike device intended for use in spreading dental resin on a tooth during application of tooth shade material. (b) Classification. Class I (general controls). The device is exempt from...

  6. Improved high-temperature resistant matrix resins

    NASA Technical Reports Server (NTRS)

    Green, H. E.; Chang, G. E.; Wright, W. F.; Ueda, K.; Orell, M. K.

    1989-01-01

    A study was performed with the objective of developing matrix resins that exhibit improved thermo-oxidative stability over state-of-the-art high temperature resins for use at temperatures up to 644 K (700 F) and air pressures up to 0.7 MPa (100 psia). The work was based upon a TRW discovered family of polyimides currently licensed to and marketed by Ethyl Corporation as EYMYD(R) resins. The approach investigated to provide improved thermo-oxidative properties was to use halogenated derivatives of the diamine, 2, 2-bis (4-(4-aminophenoxy)phenyl) hexafluoropropane (4-BDAF). Polyimide neat resins and Celion(R) 12,000 composites prepared from fluorine substituted 4-BDAF demonstrated unexpectedly lower glass transition temperatures (Tg) and thermo-oxidative stabilities than the baseline 4-BDAF/PMDA polymer.

  7. 40 CFR 414.40 - Applicability; description of the thermoplastic resins subcategory.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... the products classified under SIC 28213 thermoplastic resins including those resins and resin groups... Butyrates Cellulose Acetate Resin *Cellulose Acetates *Cellulose Acetates Propionates Cellulose Nitrate... Polymers Nylon 11 Resin *Nylon 6-66 Copolymers *Nylon 6—Nylon 11 Blends Nylon 6 Resin Nylon 612 Resin...

  8. 40 CFR 414.40 - Applicability; description of the thermoplastic resins subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... the products classified under SIC 28213 thermoplastic resins including those resins and resin groups... Butyrates Cellulose Acetate Resin *Cellulose Acetates *Cellulose Acetates Propionates Cellulose Nitrate... Polymers Nylon 11 Resin *Nylon 6-66 Copolymers *Nylon 6—Nylon 11 Blends Nylon 6 Resin Nylon 612 Resin...

  9. 40 CFR 414.40 - Applicability; description of the thermoplastic resins subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... the products classified under SIC 28213 thermoplastic resins including those resins and resin groups... Butyrates Cellulose Acetate Resin *Cellulose Acetates *Cellulose Acetates Propionates Cellulose Nitrate... Polymers Nylon 11 Resin *Nylon 6-66 Copolymers *Nylon 6—Nylon 11 Blends Nylon 6 Resin Nylon 612 Resin...

  10. 40 CFR 414.40 - Applicability; description of the thermoplastic resins subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... the products classified under SIC 28213 thermoplastic resins including those resins and resin groups... Butyrates Cellulose Acetate Resin *Cellulose Acetates *Cellulose Acetates Propionates Cellulose Nitrate... Polymers Nylon 11 Resin *Nylon 6-66 Copolymers *Nylon 6—Nylon 11 Blends Nylon 6 Resin Nylon 612 Resin...

  11. 40 CFR 414.40 - Applicability; description of the thermoplastic resins subcategory.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... the products classified under SIC 28213 thermoplastic resins including those resins and resin groups... Butyrates Cellulose Acetate Resin *Cellulose Acetates *Cellulose Acetates Propionates Cellulose Nitrate... Polymers Nylon 11 Resin *Nylon 6-66 Copolymers *Nylon 6—Nylon 11 Blends Nylon 6 Resin Nylon 612 Resin...

  12. Radiation testing of organic ion exchange resins

    SciTech Connect

    Carlson, C.D.; Bray, L.A.; Bryan, S.A.

    1995-09-01

    A number of ion exchange materials are being evaluated as part of the Tank Waste Remediation System (TWRS) Pacific Northwest Laboratory (PNL) Pretreatment Project for the removal of {sup 137}Cs from aqueous tank wastes. Two of these materials are organic resins; a phenol-formaldehyde resin (Duolite CS-100) produced by Rohm and Haas Co. (Philadelphia, Pennsylvania) and a resorcinol-formaldehyde (RF) resin produced by Boulder Scientific Co. (Mead, Colorado). One of the key parameters in the assessment of the organic based ion exchange materials is its useful lifetime in the radioactive and chemical environment that will be encountered during waste processing. The focus of the work presented in this report is the radiation stability of the CS-100 and the RF resins. The scope of the testing included one test with a sample of the CS-100 resin and testing of two batches of the RF resin (BSC-187 and BSC-210). Samples of the exchangers were irradiated with a {sup 60}Co source to a total absorbed dose of 10{sup 9} R over a period of 5 months in a static (no flow) and a flowing configuration with neutralized current acid waste (NCAW) simulant as a feed. Based on a maximum concentration of {sup 137}Cs on the resin that would result from processing NCAW, this dose represents an operational period of at least 150 days for the RF resin and at least 1260 days for the CS-100 resin. Gas generation in the static experiment was continuously monitored and G values (molecules of gas per 100 eV) were determined for each species. Resin samples were obtained periodically and the equilibrium behavior of the resins was assessed by determining the distribution coefficients (K{sub d}s). Structural information was also obtained by {sup 13}C cross polarization magic angle (CPMAS) nuclear magnetic resonance (NMR) spectrometry and Fourier Transform Infrared (FTIR) spectroscopy so that changes to the chemical structure could be correlated with changes in K{sub d}.

  13. Cesium-specific phenolic ion exchange resin

    DOEpatents

    Bibler, Jane P.; Wallace, Richard M.

    1995-01-01

    A phenolic, cesium-specific, cation exchange resin is prepared by neutralizing resorcinol with potassium hydroxide, condensing/polymerizing the resulting intermediate with formaldehyde, heat-curing the resulting polymer to effect cross-linking and grinding it to desired particle size for use. This resin will selectively and efficiently adsorb cesium ions in the presence of a high concentration of sodium ions with a low carbon to cesium ratio.

  14. Cesium-specific phenolic ion exchange resin

    DOEpatents

    Bibler, J.P.; Wallace, R.M.

    1995-08-15

    A phenolic, cesium-specific, cation exchange resin is prepared by neutralizing resorcinol with potassium hydroxide, condensing/polymerizing the resulting intermediate with formaldehyde, heat-curing the resulting polymer to effect cross-linking and grinding it to desired particle size for use. This resin will selectively and efficiently adsorb cesium ions in the presence of a high concentration of sodium ions with a low carbon to cesium ratio. 2 figs.

  15. Cleanup of TMI-2 demineralizer resins

    SciTech Connect

    Bond, W.D.; King, L.J.; Knauer, J.B.; Hofstetter, K.J.; Thompson, J.D.

    1985-01-01

    Radiocesium is being removed from Demineralizers A and B (DA and DB by a process that was developed from laboratory tests on small samples of resin from the demineralizers. The process was designed to elute the radiocesium from the demineralizer resins and then to resorb it onto the zeolite ion exchangers contained in the Submerged Demineralizer System (SDS). The process was also required to limit the maximum cesium activities in the resin eluates (SDS feeds) so that the radiation field surrounding the pipelines would not be excessive. The process consists of 17 stages of batch elution. In the initial stage, the resin is contacted with 0.18 M boric acid. Subsequent stages subject the resin to increasing concentrations of sodium in NaH/sub 2/BO/sub 3/-H/sub 3/BO/sub 3/ solution (total B = 0.35 M) and then 1 M sodium hydroxide in the final stages. Results on the performance of the process in the cleanup of the demineralizers at TMI-2 are compared to those obtained from laboratory tests with small samples of the DA and DB resins. To date, 15 stages of batch elution have been completed on the demineralizers at TMI-2 which resulted in the removal of about 750 Ci of radiocesium from DA and about 3300 Ci from DB.

  16. Ion Exchange Temperature Testing with SRF Resin

    SciTech Connect

    Russell, Renee L.; Rinehart, Donald E.; Brown, Garrett N.; Peterson, Reid A.

    2012-03-01

    Ion exchange using the Spherical Resorcinol-Formaldehyde (SRF) resin has been selected by the U.S. Department of Energy’s Office of River Protection for use in the Pretreatment Facility of the Hanford Tank Waste Treatment and Immobilization Plant (WTP) and for potential application in an at-tank deployment for removing 137Cs. Recent proposed changes to the WTP ion exchange process baseline indicate that higher temperatures (50°C) to alleviate post-filtration precipitation issues prior to reaching the ion exchange columns may be required. Therefore, it is important to understand the behavior of SRF resin performance under the conditions expected with the new equipment and process changes. This research examined the impact of elevated temperature on resin loading and resin degradation during extended solution flow using elevated temperature (45°, 50°, 55°, 60°, 65°, 75°C). Testing for extended times at elevated temperatures showed that the resin does degrade and loading capacity is reduced at and above 45°C. Above 60°C the resin appears to not load at all.

  17. Imide modified epoxy matrix resins

    NASA Technical Reports Server (NTRS)

    Scola, D. A.

    1984-01-01

    The results of a program designed to develop tough imide modified epoxy resins cured by bisimide amine (BIA) hardeners are described. State-of-the-art epoxides MY720 and DER383 were used, and four bismide amines were evaluated. These were the BIA's derived from the 6F anhydride (4,4'-(hexafluoroisopropylidene) bis(phthalic anhydride) and the diamines 3,3'-diaminodiphynyl sulfone, 4,4'-oxygianiline, 4,4'-methylene dianiline, and 1,12-dodecane diamine. A key intermediate, designated 6F anhydride, is required for the synthesis of the bisimide amines. Reaction parameters to synthesize a precursor to the 6F anhydride (6FHC) in high yields were investigated. The catalyst trifluoromethane sulfonic acid was studied. Although small scale runs yielded the 6FHC in 50 percent yield, efforts to ranslate these results to a larger scale synthesis gave the 6FHC in only 9 percent yield. Results show that the concept of using bisimide amine as curing agents to improve the toughness properties of epoxies is valid.

  18. Preparation and cured properties of novel cycloaliphatic epoxy resins

    SciTech Connect

    Tokizawa, Makoto; Okada, Hiroyoshi; Wakabayashi, Nobukatsu; Kimura, Tomiaki . Research Center)

    1993-10-20

    Preparation and characterization of novel cycloaliphatic epoxy resins, which are derived from octadienyl compounds, were studied. From a model peracetic acid epoxidation reaction using 2,7-octadienyl acetate-1, the structure of the liquid resins is estimated to be mainly terminal epoxides and some amount of inner epoxide depending on the epoxide content. The epoxy resins offer lower toxicity and lower vapor pressure. The reactivity of the resin with acid anhydrides is moderate but faster than that of traditional cyclohexane epoxide-type resins and slower than that of the glycidyl ester-type resins. This reactivity was also examined using model compounds. The heat deflection temperature of the hexahydro-phthalic anhydride-cured resins is shown to be directly proportional to the number of epoxy groups in the molecules. The flexural strength of the cured resins is nearly equivalent to that of the commercial resins, although the flexural elongation of the resins is larger than that of the rigid cyclohexane epoxide-type resins. The thermal stability of the cured resins is compared to typical rigid cycloaliphatic resins; furthermore, high water resistance of the cured resins is suggested to be attributed to the hydrophobic character of the C[sub 8] chain by cross-linking.

  19. Tc-99 Ion Exchange Resin Testing

    SciTech Connect

    Valenta, Michelle M.; Parker, Kent E.; Pierce, Eric M.

    2010-08-01

    Pacific Northwest National Laboratory was contracted by CHPRC to evaluate the release of 99Tc from spent resin used to treat water from well 299-W15-765 and stored for several years. The key questions to be answered are: 1) does 99Tc readily release from the spent ion exchange resin after being in storage for several years; 2) if hot water stripping is used to remove the co-contaminant carbon tetrachloride, will 99Tc that has been sequestered by the resin be released; and 3) can spent resin be encapsulated into a cementitious waste form; if so, how much 99Tc would be released from the weathering of the monolith waste form? The results from the long term stability leach test results confirm that the resin is not releasing a significant amount of the sequestered 99Tc, evident by the less than 0.02% of the total 99Tc loaded being identified in the solution. Furthermore, it is possible that the measured 99Tc concentration is the result of 99Tc contained in the pore spaces of the resin. In addition to these results, analyses conducted to examine the impact of hot water on the release of 99Tc suggest that only a small percentage of the total is being released. This suggest that hot water stripping to remove carbon tetrachloride will not have a significant affect on the resin’s ability to hold-on to sequestered 99Tc. Finally, encapsulation of spent resin in a cementitious material may be a viable disposal option, but additional tests are needed to examine the extent of physical degradation caused by moisture loss and the effect this degradation process can have on the release of 99Tc.

  20. Resin flow monitoring in vacuum-assisted resin transfer molding using optical fiber distributed sensor

    NASA Astrophysics Data System (ADS)

    Eum, Soohyun; Kageyama, Kazuro; Murayama, Hideaki; Ohsawa, Isamu; Uzawa, Kiyoshi; Kanai, Makoto; Igawa, Hirotaka

    2007-04-01

    In this study, we implemented resin flow monitoring by using an optical fiber sensor during vacuum assisted resin transfer molding (VaRTM).We employed optical frequency domain reflectometry (OFDR) and fiber Bragg grating (FBG) sensor for distributed sensing. Especially, long gauge FBGs (about 100mm) which are 10 times longer than an ordinary FBG were employed for more effective distributed sensing. A long gauge FBG was embedded in GFRP laminates, and other two ones were located out of laminate for wavelength reference and temperature compensation, respectively. During VaRTM, the embedded FBG could measure how the preform affected the sensor with vacuum pressure and resin was flowed into the preform. In this study, we intended to detect the gradient of compressive strain between impregnated part and umimpregnated one within long gauge FBG. If resin is infused to preform, compressive strain which is generated on FBG is released by volume of resin. We could get the wavelength shift due to the change of compressive strain along gauge length of FBG by using short-time Fourier transformation for signal acquired from FBG. Therefore, we could know the resin flow front with the gradient of compressive strain of FBG. In this study, we used silicon oil which has same viscosity with resin substitute for resin in order to reuse FBG. In order to monitor resin flow, the silicon oil was infused from one edge of preform, the silicon oil was flowed from right to left. Then, we made dry spot within gauge length by infusing silicon oil to both sides of preform to prove the ability of dry spot monitoring with FBG. We could monitor resin flow condition and dry spot formation successfully using by FBG based on OFDR.

  1. Characterization of Polyimide Matrix Resins and Prepregs

    NASA Technical Reports Server (NTRS)

    Maximovich, M. G.; Galeos, R. M.

    1985-01-01

    Graphite/polyimide composite materials are attractive candidates for a wide range of aerospace applications. They have many of the virtues of graphite/epoxies, i.e., high specific strengths and stiffness, and also outstanding thermal/oxidative stability. Yet they are not widely used in the aerospace industry due to problems of procesability. By their nature, modern addition polyimide (PI) resins and prepregs are more complex than epoxies; the key to processing lies in characterizing and understanding the materials. Chemical and rheological characterizations are carried out on several addition polyimide resins and graphite reinforced prepregs, including those based on PMR-15, LARC 160 (AP 22), LARC 160 (Curithane 103) and V378A. The use of a high range torque transducer with a Rheometrics mechanical spectrometer allows rheological data to be generated on prepreg materials as well as neat resins. The use of prepreg samples instead of neat resins eliminates the need for preimidization of the samples and the data correlates well with processing behavior found in the shop. Rheological characterization of the resins and prepregs finds significant differences not readily detected by conventional chemical characterization techniques.

  2. Diffusion of residual monomer in polymer resins.

    PubMed Central

    Piver, W T

    1976-01-01

    A simplified mathematical model which made use of Fick's laws of diffusion written in spherical coordinates was developed to describe the rate of diffusion of residual monomers from polymer resins. The properties of the monomer-polymer system which influenced the amount of monomer remaining in the polymer as a function of time were the diffusivity and solubility of the monomer in the polymer, and the particle size of the polymer resin. This model was used to analyze literature data on the diffusion of residual vinyl chloride monomer in polyvinyl chloride resins made by the suspension process. It was concluded that particle size of the resin was a significant parameter which should be taken advantage of in process equipment designed to remove residual monomer from PVC resins. The diffusivity of the monomer in the polymer was a function of the solubility of the monomer in the polymer. Monomer solubility can be determined from Henry's law. It was suggested that this model could be adapted to describe diffusion of monomers from any monomer-polymer system, and would be a useful approach to modeling the transport of nonreactive chemical additives from plastics. PMID:1026410

  3. Polymerization characteristics of EMA-based resin.

    PubMed

    Saito, Yuji

    2004-03-01

    To explore the feasibility of a new relining material, polymerization characteristics such as peak temperature, setting time, residual monomer, and postpolymerization were examined in ethyl methacrylate (EMA) resins composed of EMA and 4 kinds of EMA/methyl methacrylate (MMA) copolymers with high and low molecular weights and initiated by benzoyl peroxide/N,N-dimethyl-p-toluidine system and compared with those of MMA/PMMA resins. Peak temperature (53.8-71.0 degrees C) and residual monomer (2.56-3.52% after 1 h and 1.57-2.31% after 24 h) of the EMA resins were significantly lower than those of the MMA resins (88.9-93.4 degrees C and 4.61-5.85% after 1 h and 4.09-4.84% after 24 h, respectively). The composition of the copolymers had a significant effect on peak temperature and setting time but no significant effect on residual monomer and postpolymerization. The molecular weight of the copolymers affected peak temperature, setting time and residual monomer significantly. This study suggested that EMA resins are worthy of further evaluation as a relining material. PMID:15164919

  4. Water transport into epoxy resins and composites

    SciTech Connect

    Tsou, H.S.

    1987-01-01

    The processing-property relationships were established for the epoxy system of tetraglycidyl 4,4'-diaminodiphenyl methane (TGDDM) cured with diaminodiphenyl sulfone (DDS). The TGDDM-DDS epoxy system was selected for analysis as the ensuing polymer matrix is most common in high-performance fiber-reinforced epoxy composites. Experiments on water transport in epoxy resins with varying compositions were performed and a relaxation-coupled transport behavior was observed in these epoxy resins. By post-curing vitrified epoxy resins, the additional free volume usually measured in them was removed and maximum water uptake was reduced. Since epoxy resins were in a quasi-equilibrium glassy state after the post-cure, Fick's law with a constant diffusion coefficient could adequately describe the water sorption behavior. A network formation model based on the branching theory was developed, taking into account the difference in reactivities of primary and secondary amines and the etherification reaction. Using this network formation model, water uptake in post-cured epoxy resins was found to be proportional to tertiary amine concentration.

  5. Development of a heterogeneous laminating resin system

    NASA Technical Reports Server (NTRS)

    Biermann, T. F.; Hopper, L. C.

    1985-01-01

    The factors which effect the impact resistance of laminating resin systems and yet retain equivalent performance with the conventional 450 K curing epoxy matrix systems in other areas were studied. Formulation work was conducted on two systems, an all-epoxy and an epoxy/bismaleimide, to gain fundamental information on the effect formulation changes have upon neat resin and composite properties. The all-epoxy work involved formulations with various amounts and combinations of eight different epoxy resins, four different hardeners, fifteen different toughening agents, a filler, and a catalyst. The epoxy/bismaleimide effort improved formulations with various amounts and combinations of nine different resins, four different hardeners, eight different toughening agents, four different catalysts, and a filler. When a formulation appeared to offer the proper combination of properties required for a laminating resin Celion 3K-70P fabric was prepregged. Initial screening tests on composites primarily involved Gardner type impact and measurement of short beam shear strengths under dry and hot/wet conditions.

  6. Biocompatibility of polymethylmethacrylate resins used in dentistry.

    PubMed

    Gautam, Rupali; Singh, Raghuwar D; Sharma, Vinod P; Siddhartha, Ramashanker; Chand, Pooran; Kumar, Rakesh

    2012-07-01

    Biocompatibility or tissue compatibility describes the ability of a material to perform with an appropriate host response when applied as intended. Poly-methylmethacrylate (PMMA) based resins are most widely used resins in dentistry, especially in fabrication of dentures and orthodontic appliances. They are considered cytotoxic on account of leaching of various potential toxic substances, most common being residual monomer. Various in vitro and in vivo experiments and cell based studies conducted on acrylic based resins or their leached components have shown them to have cytotoxic effects. They can cause mucosal irritation and tissue sensitization. These studies are not only important to evaluate the long term clinical effect of these materials, but also help in further development of alternate resins. This article reviews information from scientific full articles, reviews, or abstracts published in dental literature, associated with biocompatibility of PMMA resins and it is leached out components. Published materials were searched in dental literature using general and specialist databases, like the PubMED database. PMID:22454327

  7. Color stability of composite resin cements.

    PubMed

    Smith, Darrell S; Vandewalle, Kraig S; Whisler, Gerry

    2011-01-01

    This study sought to determine the difference in color stability of resin cements after one year of storage in water. Three commercial resin cements (Nexus 3, Calibra, Variolink 2) were evaluated under three different curing conditions (photo-, dual-, and self-cure) over three storage time periods (3, 6, and 12 months). A plastic mold was used to prepare cylindrical specimens of each of the three resin cements. For the phototcured specimens, only the base component of the resin cement was cured. For the dual- and self-cure specimens, the base and catalyst of the cements were mixed according to the manufacturer's instructions, syringed into the mold, and either photocured as before (dual-cure) or allowed to chemically set (self-cure). The total amount of color change (delta E) was calculated using a spectrophotometer after 24 hours (baseline) and after 3, 6, and 12 months of storage in distilled water. Data were analyzed using a repeated measures ANOVA and a Tukey test. After one year of storage, Nexus 3 demonstated the lowest color change values (delta E) under all curing conditions, although it was not significantly different from Variolink 2 when photocured or Calibra when self-cured. New resin cements without a traditional benzoyl peroxide/amine redox initiator system, such as Nexus 3, could be more color-stable over time. PMID:22313825

  8. Ponderosa pine resin defenses and growth: metrics matter.

    PubMed

    Hood, Sharon; Sala, Anna

    2015-11-01

    Bark beetles (Coleoptera: Curculionidae, Scolytinae) cause widespread tree mortality in coniferous forests worldwide. Constitutive and induced host defenses are important factors in an individual tree's ability to survive an attack and in bottom-up regulation of bark beetle population dynamics, yet quantifying defense levels is often difficult. For example, in Pinus spp., resin flow is important for resistance to bark beetles but is extremely variable among individuals and within a season. While resin is produced and stored in resin ducts, the specific resin duct metrics that best correlate with resin flow remain unclear. The ability and timing of some pine species to produce induced resin is also not well understood. We investigated (i) the relationships between ponderosa pine (Pinus ponderosa Lawson & C. Lawson) resin flow and axial resin duct characteristics, tree growth and physiological variables, and (ii) if mechanical wounding induces ponderosa pine resin flow and resin ducts in the absence of bark beetles. Resin flow increased later in the growing season under moderate water stress and was highest in faster growing trees. The best predictors of resin flow were nonstandardized measures of resin ducts, resin duct size and total resin duct area, both of which increased with tree growth. However, while faster growing trees tended to produce more resin, models of resin flow using only tree growth were not statistically significant. Further, the standardized measures of resin ducts, density and duct area relative to xylem area, decreased with tree growth rate, indicating that slower growing trees invested more in resin duct defenses per unit area of radial growth, despite a tendency to produce less resin overall. We also found that mechanical wounding induced ponderosa pine defenses, but this response was slow. Resin flow increased after 28 days, and resin duct production did not increase until the following year. These slow induced responses may allow

  9. [Application of composite resin inlays to deciduous molars--a clinical observation of the resin onlay].

    PubMed

    Yamamoto, H; Iyori, H; Kanomi, R; Yao, K; Hieda, T

    1990-01-01

    Although composite resin has been used as an aesthetic restorative material, wear and fracture of the resin of fracture of the tooth structure are likely to occur when the size of the dental cavities are large. In addition to the lack of the aesthetic value, clinical results of prefabricated metal crown revealed several problems which were caused by the wear of the metal and the ill-adaptation of the cervical margin. In the present study, 50 devitalized deciduous molars were treated with composite resin onlays which were designed to cover the entire occlusal surface of the deciduous molar, and the clinical results were evaluated for a 6 month period. Additionally, for the purpose of simplification of the laboratory process for making resin onlays, ready-made occlusal shells were fabricated. The variety of the prepared shell size consisted of 7 sizes for the first deciduous molar, 9 sizes for the upper second deciduous molar and 10 sizes for the lower deciduous molar. The following results were obtained. 1) A partial resin fracture at the peripheral area of the mesio-buccal cuspid was found in five cases out of 50. 2) A glossy appearance on the surface of the onlay which was created by coated unfilled resin disappeared after 6 months of observation. 3) In relation to the resin onlay, when the antagonistic tooth was restored with prefabricated metal crowns, holes were made by attrition on all the crowns within a 3-4 month period.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:2133972

  10. Composite resin in medicine and dentistry.

    PubMed

    Stein, Pamela S; Sullivan, Jennifer; Haubenreich, James E; Osborne, Paul B

    2005-01-01

    Composite resin has been used for nearly 50 years as a restorative material in dentistry. Use of this material has recently increased as a result of consumer demands for esthetic restorations, coupled with the public's concern with mercury-containing dental amalgam. Composite is now used in over 95% of all anterior teeth direct restorations and in 50% of all posterior teeth direct restorations. Carbon fiber reinforced composites have been developed for use as dental implants. In medicine, fiber-reinforced composites have been used in orthopedics as implants, osseous screws, and bearing surfaces. In addition, hydroxyapatite composite resin has become a promising alternative to acrylic cement in stabilizing fractures and cancellous screw fixation in elderly and osteoporotic patients. The use of composite resin in dentistry and medicine will be the focus of this review, with particular attention paid to its physical properties, chemical composition, clinical applications, and biocompatibility. PMID:16393132

  11. Jetted mixtures of particle suspensions and resins

    NASA Astrophysics Data System (ADS)

    Hoath, S. D.; Hsiao, W.-K.; Hutchings, I. M.; Tuladhar, T. R.

    2014-10-01

    Drop-on-demand (DoD) ink-jetting of hard particle suspensions with volume fraction Φ ˜ 0.25 has been surveyed using 1000 ultra-high speed videos as a function of particle size (d90 = 0.8—3.6 μm), with added 2 wt. % acrylic (250 kDa) or 0.5 wt. % cellulose (370 kDa) resin, and also compared with Newtonian analogues. Jet break-off times from 80 μm diameter nozzles were insensitive (120 ± 10 μs) to particle size, and resin jet break-off times were not significantly altered by >30 wt. % added particles. Different particle size grades can be jetted equally well in practice, while resin content effectively controls DoD break-off times.

  12. Improved high temperature resistant matrix resins

    NASA Technical Reports Server (NTRS)

    Chang, G. E.; Powell, S. H.; Jones, R. J.

    1983-01-01

    The objective was to develop organic matrix resins suitable for service at temperatures up to 644 K (700 F) and at air pressures up to 0.4 MPa (60 psia) for time durations of a minimum of 100 hours. Matrix resins capable of withstanding these extreme oxidative environmental conditions would lead to increased use of polymer matrix composites in aircraft engines and provide significant weight and cost savings. Six linear condensation, aromatic/heterocyclic polymers containing fluorinated and/or diphenyl linkages were synthesized. The thermo-oxidative stability of the resins was determined at 644 K and compressed air pressures up to 0.4 MPa. Two formulations, both containing perfluoroisopropylidene linkages in the polymer backbone structure, exhibited potential for 644 K service to meet the program objectives. Two other formulations could not be fabricated into compression molded zero defect specimens.

  13. Resin additive improves performance of high-temperature hydrocarbon lubricants

    NASA Technical Reports Server (NTRS)

    Johnson, R. L.; Loomis, W. R.

    1971-01-01

    Paraffinic resins, in high temperature applications, improve strength of thin lubricant film in Hertzian contacts even though they do not increase bulk oil viscosity. Use of resin circumvents corrosivity and high volatility problems inherent with many chemical additives.

  14. REDFORD CORE MAKING MACHINE. RESIN IMPREGNATED SAND IS BLOWN INTO ...

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

    REDFORD CORE MAKING MACHINE. RESIN IMPREGNATED SAND IS BLOWN INTO THE HEATED CORE BOX THAT SETS THE RESIN CREATING THE HARDENED CORE SHOWN HERE. - Southern Ductile Casting Company, Core Making, 2217 Carolina Avenue, Bessemer, Jefferson County, AL

  15. Try-in Pastes Versus Resin Cements: A Color Comparison.

    PubMed

    Vaz, Edenize Cristina; Vaz, Maysa Magalhães; Rodrigues Gonçalves de Oliveira, Maria Beatriz; Takano, Alfa Emília; de Carvalho Cardoso, Paula; de Torres, Érica Miranda; Gonzaga Lopes, Lawrence

    2016-05-01

    This study aimed to compare the color of ceramic veneer restorations using different shades of try-in pastes and resin cement. Researchers found no differences between try-in pastes and resin cements after cementation. PMID:27213935

  16. Additive effects on the toughening of unsaturated polyester resins

    SciTech Connect

    Suspene, L.; Yang, Y.S.; Pascault, J.P.

    1993-12-31

    An elastomer additive, carboxy-terminated acrylonitrile-butadiene copolymer, was used for toughening in the free radical cross-linking copolymerization of unsaturated polyester (UP) resins. For molded parts, Charpy impact behavior was generally enhanced and the number of catastrophic failures was reduced. The miscibility and interfacial properties of additive and resin blends play important roles in the toughening process. Phase-diagram studies showed that the elastomer additive is immiscible with the UP resin and is phase-separated from the resin matrix during curing. This phase-separation phenomenon is similar to that in the low-profile mechanism of UP resins. Additive-resin system miscibility greatly influences curing morphology. Microvoids occurred in the additive phase of cured resin because of shrinkage stress. The intrinsic inhomogeneity of the polyester network and the existence of microvoids in the final product limit the toughening effect of additives on unsaturated polyester resins. 49 refs., 13 figs., 3 tabs.

  17. Effect of resin monomer composition on toothbrush wear resistance.

    PubMed

    Kawai, K; Iwami, Y; Ebisu, S

    1998-04-01

    The purpose of this study was to compare the toothbrush abrasion resistance of seven different experimental resins which were made by changing the composition of resin monomers. The experimental resins were made by mixing four kinds of dental resin monomers (Bis-GMA, UDMA, TMPT and TEGDMA), camphorquinone (1 wt%), dimethylaminoethyl methacrylate (2 wt%) and 2,6-di-tert-butyl-p-cresol (0.05 wt%). The resin specimens were stored in air for 2 weeks, and then put on a toothbrush abrasion testing machine. After 100000 strokes, the wear loss of each specimen was determined by weight change during the wear test. TMPT-TEGDMA resin showed the most wear resistance, while Bis-GMA- and UDMA-based resins showed increased wear resistance with an increased content of TEGDMA. Also, a inverse relationship between the microhardness number and the amount of wear of the respective resins was confirmed. PMID:9610853

  18. Performance Properties of Graphite Reinforced Composites with Advanced Resin Matrices

    NASA Technical Reports Server (NTRS)

    Kourtides, Demetrius A.

    1980-01-01

    This article looks at the effect of different resin matrices on thermal and mechanical properties of graphite composites, and relates the thermal and flammability properties to the anaerobic char yield of the resins. The processing parameters of graphite composites utilizing graphite fabric and epoxy or other advanced resins as matrices are presented. Thermoset resin matrices studied were: aminecured polyfunctional glycidyl aminetype epoxy (baseline), phenolicnovolac resin based on condensation of dihydroxymethyl-xylene and phenol cured with hexamine, two types of polydismaleimide resins, phenolic resin, and benzyl resin. The thermoplastic matrices studied were polyethersulfone and polyphenylenesulfone. Properties evaluated in the study included anaerobic char yield, limiting oxygen index, smoke evolution, moisture absorption, and mechanical properties at elevated temperatures including tensile, compressive, and short-beam shear strengths. Generally, it was determined that graphite composites with the highest char yield exhibited optimum fire-resistant properties.

  19. Standard tests for toughened resin composites, revised edition

    NASA Technical Reports Server (NTRS)

    1983-01-01

    Several toughened resin systems are evaluated to achieve commonality for certain kinds of tests used to characterize toughened resin composites. Specifications for five tests were standardized; these test standards are described.

  20. PMR Resin Compositions For High Temperatures

    NASA Technical Reports Server (NTRS)

    Vannucci, Raymond D.

    1989-01-01

    Report describes experiments to identify polymer matrix resins suitable for making graphite-fiber laminates used at 700 degree F (371 degree C) in such applications as aircraft engines to achieve higher thrust-to-weight ratios. Two particular high-molecular-weight formulations of PMR (polymerization of monomer reactants) resins most promising. PMR compositions of higher FMW exhibit enhanced thermo-oxidative stability. Formation of high-quality laminates with these compositions requires use of curing pressures higher than those suitable for compositions of lower FMW.

  1. Electronic structure and optical properties of resin

    NASA Astrophysics Data System (ADS)

    Rao, Zhi-Fan; Zhou, Rong-Feng

    2013-03-01

    We used the density of functional theory (DFT) to study the electronic structure and density of states of resin by ab initio calculation. The results show the band gap of resin is 1.7 eV. The covalent bond is combined C/O atoms with H atoms. The O 2p orbital is the biggest effect near the Fermi level. The results of optical properties show the reflectivity is low, and the refractive index is 1.7 in visible light range. The highest absorption coefficient peak is in 490 nm and the value is 75,000.

  2. New phosphorus-containing bisimide resins

    NASA Technical Reports Server (NTRS)

    Varma, I. K.; Fohlen, G. M.; Hsu, M.-T.; Parker, J. A.

    1984-01-01

    Phosphorus-based flame retardants have been effectively used in a wide variety of polymeric materials. Such additives, however, may either influence the decomposition reaction in polymers or lack durability due to a tendency to be leached out by solvents. Attention is given to the synthesis, characterization, thermal stability and degradation mechanisms of bisimide resins, and an evaluation is conducted of the flammability and mechanical properties of graphite cloth-reinforced laminates fabricated from one of the six phosphorus-containing bisimide resins considered.

  3. Resin transfer molding of textile composites

    NASA Technical Reports Server (NTRS)

    Falcone, Anthony; Dursch, Harry; Nelson, Karl; Avery, William

    1993-01-01

    The design and manufacture of textile composite panels, tubes, and angle sections that were provided to NASA for testing and evaluation are documented. The textile preform designs and requirements were established by NASA in collaboration with Boeing and several vendors of textile reinforcements. The following four types of preform architectures were used: stitched uniweave, 2D-braids, 3D-braids, and interlock weaves. The preforms consisted primarily of Hercules AS4 carbon fiber; Shell RSL-1895 resin was introduced using a resin transfer molding process. All the finished parts were inspected using ultrasonics.

  4. Benzonorbornadiene end caps for PMR resins

    NASA Technical Reports Server (NTRS)

    Panigot, Michael J.; Waters, John F.; Varde, Uday; Sutter, James K.; Sukenik, Chaim N.

    1992-01-01

    Several ortho-disubstituted benzonorbornadiene derivatives are described. These molecules contain acid, ester, or anhydride functionality permitting their use as end caps in PMR (polymerization of monomer reactants) polyimide systems. The replacement of the currently used norbornenyl end caps with benzonorbornadienyl end caps affords resins of increased aromatic content. It also allows evaluation of some mechanistic aspects of PMR cross-linking. Initial testing of N-phenylimide model compounds and of actual resin formulations using the benzonorbornadienyl end cap reveals that they undergo efficient thermal crosslinking to give oligomers with physical properties and thermal stability comparable to commercial norbornene-end-capped PMR systems.

  5. Technical assessment for quality control of resins

    NASA Technical Reports Server (NTRS)

    Gosnell, R. B.

    1977-01-01

    Survey visits to companies involved in the manufacture and use of graphite-epoxy prepregs were conducted to assess the factors which may contribute to variability in the mechanical properties of graphite-epoxy composites. In particular, the purpose was to assess the contributions of the epoxy resins to variability. Companies represented three segments of the composites industry - aircraft manufacturers, prepreg manufacturers, and epoxy resin manufacturers. Several important sources of performance variability were identified from among the complete spectrum of potential sources which ranged from raw materials to composite test data interpretation.

  6. Resin Dermatitis in a Car Factory

    PubMed Central

    Engel, H. O.; Calnan, C. D.

    1966-01-01

    An outbreak of dermatitis in a car assembly factory is described; it affected 50 workers who handled rubber weatherstrips coated with an adhesive. The adhesive was found to contain para-tertiary butyl phenol (P.T.B.P.) formaldehyde resin. Of those patch tested 70% gave positive reactions to the adhesive and 65% to the resin. Improved methods of handling and personal protection succeeded in arresting the occurrence of dermatitis. Barrier creams gave no protection in these circumstances. The episode illustrates the different preventive control methods which have to be tried when dealing with a simple skin hazard which cannot be abolished. Images PMID:5904100

  7. Occupational dermatitis to epoxydic and phenolic resins.

    PubMed

    Geraut, Christian; Tripodi, Dominique; Brunet-Courtois, Béatrice; Leray, Fabrice; Geraut, Laurent

    2009-01-01

    Contact dermatitis to epoxydic and phenolic resins are the most frequent contact dermatoses due to plastics, in particular in the form of airborne dermatitis. The chemical formulas of the various components of these resins and their additives are complex and the patch tests available in the trade are insufficient and often arrive at a late stage in the progress of industry, in particular in advanced technologies like aeronautical engineering, shipbuilding or the new floor and wall coverings in buildings. This article is a review of the actions to be taken with these allergies, as well as with regards to their diagnosis, prevention and medico-legal compensation. PMID:19349256

  8. 40 CFR 721.2752 - Epoxy resin containing phosphorus (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Epoxy resin containing phosphorus... Specific Chemical Substances § 721.2752 Epoxy resin containing phosphorus (generic). (a) Chemical substance... epoxy resin containing phosphorus (PMN P-00-912) is subject to reporting under this section for...

  9. 40 CFR 721.2752 - Epoxy resin containing phosphorus (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Epoxy resin containing phosphorus... Specific Chemical Substances § 721.2752 Epoxy resin containing phosphorus (generic). (a) Chemical substance... epoxy resin containing phosphorus (PMN P-00-912) is subject to reporting under this section for...

  10. 40 CFR 721.2752 - Epoxy resin containing phosphorus (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Epoxy resin containing phosphorus... Specific Chemical Substances § 721.2752 Epoxy resin containing phosphorus (generic). (a) Chemical substance... epoxy resin containing phosphorus (PMN P-00-912) is subject to reporting under this section for...

  11. Reusable chelating resins concentrate metal ions from highly dilute solutions

    NASA Technical Reports Server (NTRS)

    Bauman, A. J.; Weetal, H. H.; Weliky, N.

    1966-01-01

    Column chromatographic method uses new metal chelating resins for recovering heavy-metal ions from highly dilute solutions. The absorbed heavy-metal cations may be removed from the chelating resins by acid or base washes. The resins are reusable after the washes are completed.

  12. Bismaleimide resins for flame resistant honeycomb sandwich panels

    NASA Technical Reports Server (NTRS)

    1978-01-01

    A 60 kg batch of Resin M751 was produced in pilot plant scale. The resin was delivered to the prepreg company as an NMP solution. 100 kg of glass-fabric prepregs were fabricated. Prepreg characteristics and curing cycles for laminate fabrication were provided. A new batch of Resin M756 (Code M756 - 2) was synthesized.

  13. 21 CFR 177.2510 - Polyvinylidene fluoride resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyvinylidene fluoride resins. 177.2510 Section... as Components of Articles Intended for Repeated Use § 177.2510 Polyvinylidene fluoride resins. Polyvinylidene fluoride resins may be safely used as articles or components of articles intended for repeated...

  14. 21 CFR 177.2510 - Polyvinylidene fluoride resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyvinylidene fluoride resins. 177.2510 Section... as Components of Articles Intended for Repeated Use § 177.2510 Polyvinylidene fluoride resins. Polyvinylidene fluoride resins may be safely used as articles or components of articles intended for repeated...

  15. 21 CFR 872.3310 - Coating material for resin fillings.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Coating material for resin fillings. 872.3310... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3310 Coating material for resin fillings. (a) Identification. A coating material for resin fillings is a device intended to be applied to...

  16. 21 CFR 872.3300 - Hydrophilic resin coating for dentures.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Hydrophilic resin coating for dentures. 872.3300... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3300 Hydrophilic resin coating for dentures. (a) Identification. A hydrophilic resin coating for dentures is a device that consists of a...

  17. 40 CFR 721.9499 - Modified silicone resin.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Modified silicone resin. 721.9499... Substances § 721.9499 Modified silicone resin. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a modified silicone resin (PMN P-96-1649)...

  18. Occupational asthma due to unheated polyvinylchloride resin dust.

    PubMed

    Lee, H S; Yap, J; Wang, Y T; Lee, C S; Tan, K T; Poh, S C

    1989-11-01

    Polyvinylchloride (PVC) resins are widely used in industry. Asthma due to the thermal degradation products of PVC are well documented. In this first case of occupational asthma due to unheated PVC resin dust the patient was exposed to PVC resin dust during the mixing of chemicals used for making plastic seals for bottle caps. PMID:2590649

  19. ELUTION OF URANIUM VALUES FROM ION EXCHANGE RESINS

    DOEpatents

    Kennedy, R.H.

    1959-11-24

    A process is described for eluting complex uranium ions absorbed on ion exchange resins. The resin is subjected to the action of an aqueous eluting solution contuining sulfuric acid and an alkali metal, ammonium, or magnesium chloride or nitrate, the elution being carried out until the desired amount of the uranium is removed from the resin.

  20. 40 CFR 721.4380 - Modified hydrocarbon resin.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Modified hydrocarbon resin. 721.4380... Substances § 721.4380 Modified hydrocarbon resin. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a modified hydrocarbon resin (P-91-1418)...

  1. 40 CFR 721.4380 - Modified hydrocarbon resin.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Modified hydrocarbon resin. 721.4380... Substances § 721.4380 Modified hydrocarbon resin. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a modified hydrocarbon resin (P-91-1418)...

  2. 40 CFR 721.4380 - Modified hydrocarbon resin.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Modified hydrocarbon resin. 721.4380... Substances § 721.4380 Modified hydrocarbon resin. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a modified hydrocarbon resin (P-91-1418)...

  3. 40 CFR 721.4380 - Modified hydrocarbon resin.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Modified hydrocarbon resin. 721.4380... Substances § 721.4380 Modified hydrocarbon resin. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a modified hydrocarbon resin (P-91-1418)...

  4. 40 CFR 721.4380 - Modified hydrocarbon resin.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Modified hydrocarbon resin. 721.4380... Substances § 721.4380 Modified hydrocarbon resin. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a modified hydrocarbon resin (P-91-1418)...

  5. 21 CFR 872.3770 - Temporary crown and bridge resin.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 8 2013-04-01 2013-04-01 false Temporary crown and bridge resin. 872.3770 Section... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3770 Temporary crown and bridge resin. (a) Identification. A temporary crown and bridge resin is a device composed of a material, such...

  6. 21 CFR 872.3770 - Temporary crown and bridge resin.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Temporary crown and bridge resin. 872.3770 Section... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3770 Temporary crown and bridge resin. (a) Identification. A temporary crown and bridge resin is a device composed of a material, such...

  7. 21 CFR 872.3770 - Temporary crown and bridge resin.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 8 2014-04-01 2014-04-01 false Temporary crown and bridge resin. 872.3770 Section... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3770 Temporary crown and bridge resin. (a) Identification. A temporary crown and bridge resin is a device composed of a material, such...

  8. 21 CFR 872.3770 - Temporary crown and bridge resin.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 8 2011-04-01 2011-04-01 false Temporary crown and bridge resin. 872.3770 Section... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3770 Temporary crown and bridge resin. (a) Identification. A temporary crown and bridge resin is a device composed of a material, such...

  9. 21 CFR 872.3770 - Temporary crown and bridge resin.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 8 2012-04-01 2012-04-01 false Temporary crown and bridge resin. 872.3770 Section... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3770 Temporary crown and bridge resin. (a) Identification. A temporary crown and bridge resin is a device composed of a material, such...

  10. 21 CFR 177.2510 - Polyvinylidene fluoride resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyvinylidene fluoride resins. 177.2510 Section... as Components of Articles Intended for Repeated Use § 177.2510 Polyvinylidene fluoride resins. Polyvinylidene fluoride resins may be safely used as articles or components of articles intended for repeated...

  11. 21 CFR 177.2510 - Polyvinylidene fluoride resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyvinylidene fluoride resins. 177.2510 Section... as Components of Articles Intended for Repeated Use § 177.2510 Polyvinylidene fluoride resins. Polyvinylidene fluoride resins may be safely used as articles or components of articles intended for repeated...

  12. 21 CFR 872.3820 - Root canal filling resin.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 8 2014-04-01 2014-04-01 false Root canal filling resin. 872.3820 Section 872...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3820 Root canal filling resin. (a) Identification. A root canal filling resin is a device composed of material, such as methylmethacrylate,...

  13. 21 CFR 872.3820 - Root canal filling resin.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 8 2012-04-01 2012-04-01 false Root canal filling resin. 872.3820 Section 872...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3820 Root canal filling resin. (a) Identification. A root canal filling resin is a device composed of material, such as methylmethacrylate,...

  14. 21 CFR 872.3820 - Root canal filling resin.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 8 2013-04-01 2013-04-01 false Root canal filling resin. 872.3820 Section 872...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3820 Root canal filling resin. (a) Identification. A root canal filling resin is a device composed of material, such as methylmethacrylate,...

  15. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyethylene resins, carboxyl modified. 177.1600... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface...

  16. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyethylene resins, carboxyl modified. 177.1600... Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface of articles intended for use in contact...

  17. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyethylene resins, carboxyl modified. 177.1600... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface...

  18. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyethylene resins, carboxyl modified. 177.1600... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface...

  19. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyethylene resins, carboxyl modified. 177.1600... Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as the food-contact surface...

  20. Synthesis and toughness properties of resins and composites

    NASA Technical Reports Server (NTRS)

    Johnston, N. J.

    1984-01-01

    Tensile and shear moduli of four ACEE (Aircraft Energy Efficiency Program) resins are presented along with ACEE composite material modulus predictions based on micromechanics. Compressive strength and fracture toughness of the resins and composites were discussed. In addition, several resin synthesis techniques are reviewed.

  1. 21 CFR 177.2420 - Polyester resins, cross-linked.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... polycondensation reaction at levels not to exceed 0.2 percent of the polyester resin. Dicumyl peroxide....2 percent of the polyester resin. Lauroyl peroxide p-Menthane hydroperoxide Methyl ethyl ketone... reaction at levels not to exceed 0.2 percent of the polyester resin. 4. Solvents for...

  2. 21 CFR 177.2420 - Polyester resins, cross-linked.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... polycondensation reaction at levels not to exceed 0.2 percent of the polyester resin. Dicumyl peroxide....2 percent of the polyester resin. Lauroyl peroxide p-Menthane hydroperoxide Methyl ethyl ketone... reaction at levels not to exceed 0.2 percent of the polyester resin. 4. Solvents for...

  3. Photosensitive filler minimizes internal stresses in epoxy resins

    NASA Technical Reports Server (NTRS)

    Dillon, J. N.

    1967-01-01

    Photosensitive filler is added to curable epoxy resins to minimize stress from internal shrinkage during curing or polymerization. Cinnamic acid resins and cinnamal ketones may be added in the amount of 1 to 3 percent by weight of the resin mixture.

  4. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Acrylamide-acrylic acid resin. 573.120 Section 573... Food Additive Listing § 573.120 Acrylamide-acrylic acid resin. Acrylamide-acrylic acid resin... acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the...

  5. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Acrylamide-acrylic acid resin. 573.120 Section 573... Food Additive Listing § 573.120 Acrylamide-acrylic acid resin. Acrylamide-acrylic acid resin... acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the...

  6. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Acrylamide-acrylic acid resin. 573.120 Section 573... Food Additive Listing § 573.120 Acrylamide-acrylic acid resin. Acrylamide-acrylic acid resin... acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the...

  7. 21 CFR 176.110 - Acrylamide-acrylic acid resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Acrylamide-acrylic acid resins. 176.110 Section 176... Substances for Use Only as Components of Paper and Paperboard § 176.110 Acrylamide-acrylic acid resins. Acrylamide-acrylic acid resins may be safely used as components of articles intended for use in...

  8. 21 CFR 176.110 - Acrylamide-acrylic acid resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Acrylamide-acrylic acid resins. 176.110 Section... Substances for Use Only as Components of Paper and Paperboard § 176.110 Acrylamide-acrylic acid resins. Acrylamide-acrylic acid resins may be safely used as components of articles intended for use in...

  9. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Acrylamide-acrylic acid resin. 573.120 Section 573... Food Additive Listing § 573.120 Acrylamide-acrylic acid resin. Acrylamide-acrylic acid resin... acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the...

  10. 21 CFR 176.110 - Acrylamide-acrylic acid resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Acrylamide-acrylic acid resins. 176.110 Section... Substances for Use Only as Components of Paper and Paperboard § 176.110 Acrylamide-acrylic acid resins. Acrylamide-acrylic acid resins may be safely used as components of articles intended for use in...

  11. 21 CFR 176.110 - Acrylamide-acrylic acid resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Acrylamide-acrylic acid resins. 176.110 Section... Substances for Use Only as Components of Paper and Paperboard § 176.110 Acrylamide-acrylic acid resins. Acrylamide-acrylic acid resins may be safely used as components of articles intended for use in...

  12. 21 CFR 872.3300 - Hydrophilic resin coating for dentures.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 8 2011-04-01 2011-04-01 false Hydrophilic resin coating for dentures. 872.3300... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3300 Hydrophilic resin coating for dentures. (a) Identification. A hydrophilic resin coating for dentures is a device that consists of a...

  13. 21 CFR 872.3310 - Coating material for resin fillings.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 8 2012-04-01 2012-04-01 false Coating material for resin fillings. 872.3310... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3310 Coating material for resin fillings. (a) Identification. A coating material for resin fillings is a device intended to be applied to...

  14. 21 CFR 872.3310 - Coating material for resin fillings.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 8 2014-04-01 2014-04-01 false Coating material for resin fillings. 872.3310... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3310 Coating material for resin fillings. (a) Identification. A coating material for resin fillings is a device intended to be applied to...

  15. 21 CFR 872.3310 - Coating material for resin fillings.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 8 2013-04-01 2013-04-01 false Coating material for resin fillings. 872.3310... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3310 Coating material for resin fillings. (a) Identification. A coating material for resin fillings is a device intended to be applied to...

  16. 21 CFR 872.3300 - Hydrophilic resin coating for dentures.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 8 2012-04-01 2012-04-01 false Hydrophilic resin coating for dentures. 872.3300... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3300 Hydrophilic resin coating for dentures. (a) Identification. A hydrophilic resin coating for dentures is a device that consists of a...

  17. 21 CFR 872.3300 - Hydrophilic resin coating for dentures.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 8 2013-04-01 2013-04-01 false Hydrophilic resin coating for dentures. 872.3300... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3300 Hydrophilic resin coating for dentures. (a) Identification. A hydrophilic resin coating for dentures is a device that consists of a...

  18. 21 CFR 872.3300 - Hydrophilic resin coating for dentures.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 8 2014-04-01 2014-04-01 false Hydrophilic resin coating for dentures. 872.3300... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3300 Hydrophilic resin coating for dentures. (a) Identification. A hydrophilic resin coating for dentures is a device that consists of a...

  19. 21 CFR 872.3310 - Coating material for resin fillings.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 8 2011-04-01 2011-04-01 false Coating material for resin fillings. 872.3310... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3310 Coating material for resin fillings. (a) Identification. A coating material for resin fillings is a device intended to be applied to...

  20. Occupational asthma due to unheated polyvinylchloride resin dust.

    PubMed Central

    Lee, H S; Yap, J; Wang, Y T; Lee, C S; Tan, K T; Poh, S C

    1989-01-01

    Polyvinylchloride (PVC) resins are widely used in industry. Asthma due to the thermal degradation products of PVC are well documented. In this first case of occupational asthma due to unheated PVC resin dust the patient was exposed to PVC resin dust during the mixing of chemicals used for making plastic seals for bottle caps. PMID:2590649

  1. 21 CFR 872.3200 - Resin tooth bonding agent.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 8 2012-04-01 2012-04-01 false Resin tooth bonding agent. 872.3200 Section 872...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3200 Resin tooth bonding agent. (a) Identification. A resin tooth bonding agent is a device material, such as methylmethacrylate, intended to be...

  2. 21 CFR 872.3690 - Tooth shade resin material.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 8 2012-04-01 2012-04-01 false Tooth shade resin material. 872.3690 Section 872...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3690 Tooth shade resin material. (a) Identification. Tooth shade resin material is a device composed of materials such as bisphenol-A...

  3. 21 CFR 872.3690 - Tooth shade resin material.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 8 2013-04-01 2013-04-01 false Tooth shade resin material. 872.3690 Section 872...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3690 Tooth shade resin material. (a) Identification. Tooth shade resin material is a device composed of materials such as bisphenol-A...

  4. 21 CFR 872.3200 - Resin tooth bonding agent.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 8 2013-04-01 2013-04-01 false Resin tooth bonding agent. 872.3200 Section 872...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3200 Resin tooth bonding agent. (a) Identification. A resin tooth bonding agent is a device material, such as methylmethacrylate, intended to be...

  5. 21 CFR 872.3200 - Resin tooth bonding agent.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 8 2014-04-01 2014-04-01 false Resin tooth bonding agent. 872.3200 Section 872...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3200 Resin tooth bonding agent. (a) Identification. A resin tooth bonding agent is a device material, such as methylmethacrylate, intended to be...

  6. 21 CFR 872.3690 - Tooth shade resin material.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 8 2011-04-01 2011-04-01 false Tooth shade resin material. 872.3690 Section 872...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3690 Tooth shade resin material. (a) Identification. Tooth shade resin material is a device composed of materials such as bisphenol-A...

  7. 21 CFR 872.3200 - Resin tooth bonding agent.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 8 2011-04-01 2011-04-01 false Resin tooth bonding agent. 872.3200 Section 872...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3200 Resin tooth bonding agent. (a) Identification. A resin tooth bonding agent is a device material, such as methylmethacrylate, intended to be...

  8. 21 CFR 872.3690 - Tooth shade resin material.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Tooth shade resin material. 872.3690 Section 872...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3690 Tooth shade resin material. (a) Identification. Tooth shade resin material is a device composed of materials such as bisphenol-A...

  9. 21 CFR 872.3690 - Tooth shade resin material.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 8 2014-04-01 2014-04-01 false Tooth shade resin material. 872.3690 Section 872...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3690 Tooth shade resin material. (a) Identification. Tooth shade resin material is a device composed of materials such as bisphenol-A...

  10. 21 CFR 177.2355 - Mineral reinforced nylon resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Mineral reinforced nylon resins. 177.2355 Section... as Components of Articles Intended for Repeated Use § 177.2355 Mineral reinforced nylon resins. Mineral reinforced nylon resins identified in paragraph (a) of this section may be safely used as...

  11. 21 CFR 177.2355 - Mineral reinforced nylon resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Mineral reinforced nylon resins. 177.2355 Section... as Components of Articles Intended for Repeated Use § 177.2355 Mineral reinforced nylon resins. Mineral reinforced nylon resins identified in paragraph (a) of this section may be safely used as...

  12. 21 CFR 177.2355 - Mineral reinforced nylon resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Mineral reinforced nylon resins. 177.2355 Section... as Components of Articles Intended for Repeated Use § 177.2355 Mineral reinforced nylon resins. Mineral reinforced nylon resins identified in paragraph (a) of this section may be safely used as...

  13. 21 CFR 177.2355 - Mineral reinforced nylon resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Mineral reinforced nylon resins. 177.2355 Section... as Components of Articles Intended for Repeated Use § 177.2355 Mineral reinforced nylon resins. Mineral reinforced nylon resins identified in paragraph (a) of this section may be safely used as...

  14. 40 CFR 721.5762 - Aromatic aldehyde phenolic resin (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Aromatic aldehyde phenolic resin... Specific Chemical Substances § 721.5762 Aromatic aldehyde phenolic resin (generic). (a) Chemical substance... aromatic aldehyde phenolic resin (PMN P-01-573) is subject to reporting under this section for...

  15. 40 CFR 721.5905 - Modified phenolic resin (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Modified phenolic resin (generic). 721... Substances § 721.5905 Modified phenolic resin (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a modified phenolic resin...

  16. 40 CFR 721.5908 - Modified phenolic resin (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Modified phenolic resin (generic). 721... Substances § 721.5908 Modified phenolic resin (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as modified phenolic resin (PMN...

  17. Low-melt Viscosity Polyimide Resins for Resin Transfer Molding (RTM) II

    NASA Technical Reports Server (NTRS)

    Chuang, Kathy C.; Criss, Jim M.; Mintz, Eric A.; Scheiman, Daniel A.; Nguyen, Baochau N.; McCorkle, Linda S.

    2007-01-01

    A series of polyimide resins with low-melt viscosities in the range of 10-30 poise and high glass transition temperatures (Tg s) of 330-370 C were developed for resin transfer molding (RTM) applications. These polyimide resins were formulated from 2,3,3 ,4 -biphenyltetracarboxylic dianhydride (a-BPDA) with 4-phenylethynylphthalic anhydride endcaps along with either 3,4 - oxyaniline (3,4 -ODA), 3,4 -methylenedianiline, (3,4 -MDA) or 3,3 -methylenedianiline (3,3 -MDA). These polyimides had pot lives of 30-60 minutes at 260-280 C, enabling the successful fabrication of T650-35 carbon fiber reinforced composites via RTM process. The viscosity profiles of the polyimide resins and the mechanical properties of the polyimide carbon fiber composites will be discussed.

  18. 21 CFR 177.1585 - Polyestercarbonate resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ..., 1985, which is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies... is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies are... resins identified in paragraph (a) of this section can be identified by their characteristic...

  19. Pharmaceutical Applications of Ion-Exchange Resins

    ERIC Educational Resources Information Center

    Elder, David

    2005-01-01

    The historical uses of ion-exchanged resins and a summary of the basic chemical principles involved in the ion-exchanged process are discussed. Specific applications of ion-exchange are provided that include drug stabilization, pharmaceutical excipients, taste-masking agents, oral sustained-release products, topical products for local application…

  20. 21 CFR 177.1580 - Polycarbonate resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polycarbonate resins. 177.1580 Section 177.1580 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food...

  1. 21 CFR 177.1580 - Polycarbonate resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... production of the resins; or by (2) The reaction of molten 4,4′-iso-propylidenediphenol with molten diphenyl... (CAS Reg. No. 599-64-4) For use only as a chain terminator at a level not to exceed 5 percent by...

  2. 21 CFR 177.1580 - Polycarbonate resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polycarbonate resins. 177.1580 Section 177.1580 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food...

  3. 21 CFR 177.1580 - Polycarbonate resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polycarbonate resins. 177.1580 Section 177.1580 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food...

  4. 21 CFR 177.1580 - Polycarbonate resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polycarbonate resins. 177.1580 Section 177.1580 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food...

  5. [Study of purity tests for silicone resins].

    PubMed

    Sato, Kyoko; Otsuki, Noriko; Ohori, Akio; Chinda, Mitsuru; Furusho, Noriko; Osako, Tsutomu; Akiyama, Hiroshi; Kawamura, Yoko

    2012-01-01

    In the 8th edition of Japan's Specifications and Standards for Food Additives, the purity test for silicone resins requires the determination of the refractive index and kinetic viscosity of the extracted silicone oil, and allows for only a limited amount of silicon dioxide. In the purity test, carbon tetrachloride is used to separate the silicone oil and silicon dioxide. To exclude carbon tetrachloride, methods were developed for separating the silicone oil and silicon dioxide from silicone resin, which use hexane and 10% n-dodecylbenzenesulfonic acid in hexane. For silicone oil, the measured refractive index and kinetic viscosity of the silicone oil obtained from the hexane extract were shown to be equivalent to those of the intact silicone oil. In regard to silicon dioxide, it was confirmed that, following the separation with 10% n-dodecylbenzenesulfonic acid in hexane, the level of silicon dioxide in silicone resin can be accurately determined. Therefore, in this study, we developed a method for testing the purity of silicone resins without the use of carbon tetrachloride, which is a harmful reagent. PMID:23243991

  6. Fiber reinforced thermoplastic resin matrix composites

    NASA Technical Reports Server (NTRS)

    Jones, Robert J. (Inventor); Chang, Glenn E. C. (Inventor)

    1989-01-01

    Polyimide polymer composites having a combination of enhanced thermal and mechanical properties even when subjected to service temperatures as high as 700.degree. F. are described. They comprise (a) from 10 to 50 parts by weight of a thermoplastic polyimide resin prepared from 2,2-bis[4-(4-aminophenoxy)phenyl]hexafluoropropane and (b) from 90 to 50 parts by weight of continuous reinforcing fibers, the total of (a) and (b) being 100 parts by weight. Composites based on polyimide resin formed from 2,2-bis[4-(4-aminophenoxy)phenyl]hexafluoropropane and pyromellitic dianhydride and continuous carbon fibers retained at least about 50% of their room temperature shear strength after exposure to 700.degree. F. for a period of 16 hours in flowing air. Preferably, the thermoplastic polyimide resin is formed in situ in the composite material by thermal imidization of a corresponding amide-acid polymer prepared from 2,2-bis[4-(4-aminophenoxy)phenyl]hexafluoropropane. It is also preferred to initially size the continuous reinforcing fibers with up to about one percent by weight of an amide-acid polymer prepared from 2,2-bis[4-(4-aminophenoxy)phenyl]hexafluoropropane. In this way imidization at a suitable elevated temperature results in the in-situ formation of a substantially homogeneous thermoplastic matrix of the polyimide resin tightly and intimately bonded to the continuous fibers. The resultant composites tend to have optimum thermo-mechanical properties.

  7. Resin char oxidation retardant for composites

    NASA Technical Reports Server (NTRS)

    Bowles, K. J.; Gluyas, R. E.

    1981-01-01

    Boron powder stabilizes char, so burned substances are shiny, smooth, and free of loose graphite fibers. Resin weight loss of laminates during burning in air is identical for the first three minutes for unfilled and boron-filled samples, then boron samples stabilize.

  8. 21 CFR 177.1330 - Ionomeric resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ionomeric resins. 177.1330 Section 177.1330 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact...

  9. Resin Characterization in Cured Composite Materials

    NASA Technical Reports Server (NTRS)

    Young, P. R.; Chang, A.

    1985-01-01

    Molecular-level characterization of polymeric matrix resin in cured graphite-reinforced composite materials now determined through analysis of diffuse reflectance (DR) with Fourier Transform Infrared (FTIR) spectroscopy. Improved analytical method based on diffuse reflectance. DR/ FTIR technique successfully applied to analysis of several different composites and adhesives impossible to analyze by conventional methods.

  10. 21 CFR 177.1680 - Polyurethane resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyurethane resins. 177.1680 Section 177.1680 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food...

  11. 21 CFR 177.1680 - Polyurethane resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyurethane resins. 177.1680 Section 177.1680 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food...

  12. 21 CFR 177.1680 - Polyurethane resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyurethane resins. 177.1680 Section 177.1680 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food...

  13. Studies on chemoviscosity modeling for thermosetting resins

    NASA Technical Reports Server (NTRS)

    Bai, J. M.; Hou, T. H.; Tiwari, S. N.

    1987-01-01

    A new analytical model for simulating chemoviscosity of thermosetting resins has been formulated. The model is developed by modifying the well-established Williams-Landel-Ferry (WLF) theory in polymer rheology for thermoplastic materials. By introducing a relationship between the glass transition temperature Tg(t) and the degree of cure alpha(t) of the resin system under cure, the WLF theory can be modified to account for the factor of reaction time. Temperature dependent functions of the modified WLF theory constants C sub 1 (t) and C sub 2 (t) were determined from the isothermal cure data. Theoretical predictions of the model for the resin under dynamic heating cure cycles were shown to compare favorably with the experimental data. This work represents progress toward establishing a chemoviscosity model which is capable of not only describing viscosity profiles accurately under various cure cycles, but also correlating viscosity data to the changes of physical properties associated with the structural transformation of the thermosetting resin systems during cure.

  14. 21 CFR 177.1555 - Polyarylate resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyarylate resins. 177.1555 Section 177.1555 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food...

  15. 21 CFR 177.1655 - Polysulfone resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polysulfone resins. 177.1655 Section 177.1655 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food...

  16. 21 CFR 177.1380 - Fluorocarbon resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... resin pellets, when extracted with 100 milliliters of distilled water at reflux temperature for 8 hours... distilled water at reflux temperature for 8 hours, shall yield total extractives not to exceed 0.003 percent... 1 CFR part 51. Copies may be obtained from the American Society for Testing and Materials, 1916...

  17. 21 CFR 177.1556 - Polyaryletherketone resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyaryletherketone resins. 177.1556 Section 177.1556 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use...

  18. 21 CFR 177.1380 - Fluorocarbon resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Fluorocarbon resins. 177.1380 Section 177.1380 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food...

  19. 21 CFR 177.1330 - Ionomeric resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ionomeric resins. 177.1330 Section 177.1330 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food...

  20. 21 CFR 177.1595 - Polyetherimide resin.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...) of this section shall have an intrinsic viscosity in chloroform at 25 °C (77 °F) of not less than 0.35 deciliter per gram as determined by a method titled “Intrinsic Viscosity of ULTEM Polyetherimide... discs of thickness 0.16 centimeter (0.063 inch). The resin discs when extracted with distilled water...

  1. Thermal expansion characteristics of light-cured dental resins and resin composites.

    PubMed

    Sideridou, Irini; Achilias, Dimitris S; Kyrikou, Eleni

    2004-07-01

    The thermal expansion characteristics of dental resins prepared by light-curing of Bis-GMA, TEGDMA, UDMA, Bis-EMA(4) or PCDMA dimethacrylate monomers and of commercial light-cured resin composites (Z-100 MP, Filtek Z-250, Sculpt-It and Alert), the organic matrix resin of which is based on different combinations of the above monomers, were studied by thermomechanical analysis (TMA). This study showed the existence of a glass transition temperature at around 35-47 degrees C for the resins and 40-45 degrees C for the composites; then the coefficient of linear thermal expansion (CLTE) was calculated at the temperature intervals 0-60 degrees C, 0-T(g) and T(g)-60 degrees C. The CLTE values of Bis-GMA, TEGDMA and UDMA resins are similar and lower than those of Bis-EMA (4) and PCDMA resins. The CLTE values of the composites indicated that the major factor that affects the CLTE of a composite is the filler content, but it also seems to be affected by the chemical structure of the matrix resin. TMA on water-saturated samples showed that water desorption takes place during the measurement and that the residual water acts as a plasticizer decreasing the T(g) and increasing the CLTE values. Furthermore, TMA on post-heated samples for 1, 3 or 6h showed, only for the resins, an initial decrease of CLTE and increase of the T(g) after 1h that was not significantly changed after 6h of heating. PMID:14967543

  2. Resin film infusion mold tooling and molding method

    NASA Technical Reports Server (NTRS)

    Burgess, Roger (Inventor); Grossheim, Brian (Inventor); Mouradian, Karbis (Inventor); Thrash, Patrick J. (Inventor)

    1999-01-01

    A mold apparatus and method for resin film infusion molding including an outer mold tool having a facing sheet adapted to support a resin film and preform assembly. The facing sheet includes attachment features extending therefrom. An inner mold tool is positioned on the facing sheet to enclose the resin film and preform assembly for resin film infusion molding. The inner mold tool includes a plurality of mandrels positioned for engagement with the resin film and preform assembly. Each mandrel includes a slot formed therein. A plurality of locating bars cooperate with the slots and with the attachment features for locating the mandrels longitudinally on the outer mold tool.

  3. NITRATE CONVERSION OF HB-LINE REILLEXTM HPQ RESIN

    SciTech Connect

    Steimke, J.; Williams, M.; Steeper, T.; Leishear, R.

    2012-05-29

    Reillex{trademark} HPQ ion exchange resin is used by HB Line to remove plutonium from aqueous streams. Reillex{trademark} HPQ resin currently available from Vertellus Specialties LLC is a chloride ionic form, which can cause stress corrosion cracking in stainless steels. Therefore, HB Line Engineering requested that Savannah River National Laboratory (SRNL) convert resin from chloride form to nitrate form in the Engineering Development Laboratory (EDL). To perform this task, SRNL treated two batches of resin in 2012. The first batch of resin from Reilly Industries Batch 80302MA was initially treated at SRNL in 2001 to remove chloride. This batch of resin, nominally 30 liters, has been stored wet in carboys since that time until being retreated in 2012. The second batch of resin from Batch 23408 consisted of 50 kg of new resin purchased from Vertellus Specialties in 2012. Both batches were treated in a column designed to convert resin using downflow of 1.0 M sodium nitrate solution through the resin bed followed by rinsing with deionized water. Both batches were analyzed for chloride concentration, before and after treatment, using Neutron Activation Analysis (NAA). The resin specification [Werling, 2003] states the total chlorine and chloride concentration shall be less than 250 ppm. The resin condition for measuring this concentration is not specified; however, in service the resin would always be fully wet. Measurements in SRNL showed that changing from oven dry resin to fully wet resin, with liquid in the particle interstices but no supernatant, increases the total weight by a factor of at least three. Therefore, concentration of chlorine or chloride expressed as parts per million (ppm) decreases by a factor of three. Therefore, SRNL recommends measuring chlorine concentration on an oven dry basis, then dividing by three to estimate chloride concentration in the fully wet condition. Chloride concentration in the first batch (No.80302MA) was nearly the same

  4. Stability Of A Carbon-Dioxide-Removing Resin

    NASA Technical Reports Server (NTRS)

    Wydeven, Theodore; Wood, Peter

    1990-01-01

    Report describes experiments determing long-term chemical stability of IRA-45, commerical ion-exchange resin candidate for use in removing CO2 from atmosphere of Space Station. In proposed system, cabin air passes through resin, and acidic CO2 absorbed by weakly-basic hydrated diethylenetriamine bonded to porous resin substrate. When resin absorbs all CO2, disconnects from airstream and heated with steam to desorb CO2. Resin reuseable. Removed by post-treating process air with phosphoric acid on charcoal. Other chemicals removed by trace-contaminant-control subsystem of Space Station.

  5. Resin systems for producing polymer concrete

    SciTech Connect

    Kukacka, L.E.

    1988-09-01

    When plastics are combined with mixtures of inorganic materials, high-strength, durable, fast-setting composites are produced. These materials are used in structural engineering and other applications, and as a result of the many commercial successes that have been achieved, considerable research and development work is in progress throughout the world. One family of polymer-based composites receiving considerable attention is called polymer concrete. Work in this area is directed toward developing new high-strength durable materials by combining cement and concrete technology with that of polymer chemistry. The purpose of this paper is to discuss the types of resins that can be used to form polymer concretes. Resin selection is normally based upon the desired properties for the composite and cost. However, the physical and chemical properties of the resins before and during curing are also important, particularly for field-applied materials. Currently, for normal temperature (0/degree/ to 30/degree/C) applications, epoxy resins, vinyl monomers such as polyester-styrene, methylmethacrylate, furfuryl alcohol, furan derivatives, urethane, and styrene, are being used. Styrene-trimethylolpropane trimethacrylate (TMPTMA) mixtures and styrene-acrylamide-TMPTMA mixtures yield composites with excellent hydrothermal stability at temperatures up to 150/degree/ and 250/degree/C, respectively, and organosiloxane resins have been successfully tested at 300/degree/C. Of equal importance is the selection of the composition of the inorganic phase of the composite, since chemical interactions between the two phases can significantly enhance the final properties. Further work to elucidate the mechanisms of these interactions is needed. 6 refs.

  6. ANALYSIS OF VENTING OF A RESIN SLURRY

    SciTech Connect

    Laurinat, J.; Hensel, S.

    2012-03-27

    A resin slurry venting analysis was conducted to address safety issues associated with overpressurization of ion exchange columns used in the Purex process at the Savannah River Site (SRS). If flow to these columns were inadvertently interrupted, an exothermic runaway reaction could occur between the ion exchange resin and the nitric acid used in the feed stream. The nitric acid-resin reaction generates significant quantities of noncondensable gases, which would pressurize the column. To prevent the column from rupturing during such events, rupture disks are installed on the column vent lines. The venting analysis models accelerating rate calorimeter (ARC) tests and data from tests that were performed in a vented test vessel with a rupture disk. The tests showed that the pressure inside the test vessel continued to increase after the rupture disk opened, though at a slower rate than prior to the rupture. Calculated maximum discharge rates for the resin venting tests exceeded the measured rates of gas generation, so the vent size was sufficient to relieve the pressure in the test vessel if the vent flow rate was constant. The increase in the vessel pressure is modeled as a transient phenomenon associated with expansion of the resin slurry/gas mixture upon rupture of the disk. It is postulated that the maximum pressure at the end of this expansion is limited by energy minimization to approximately 1.5 times the rupture disk burst pressure. The magnitude of this pressure increase is consistent with the measured pressure transients. The results of this analysis demonstrate the need to allow for a margin between the design pressure and the rupture disk burst pressure in similar applications.

  7. [New acrylic resins with very low residual monomer].

    PubMed

    Ohe, Y; Kadoma, Y; Imai, Y

    1989-07-01

    New experimental acrylic resins were prepared by polymerization of MMA in the presence of vinylidene fluoride/hexafluoropropylene copolymer. The amount of residual monomer in the resins prepared by visible light curing, cold curing, and heat curing, at various polymer/monomer ratios, was measured and compared with the usual MMA/PMMA resin. In the visible light cured resins containing 60 or 70 wt% of the fluoropolymer, the amount of residual monomer was less than 0.1%. In the cold cured resins, the amount of residual monomer was very low: 0.2% and 0.7% for the resins containing 70 and 60 wt% of the polymer, respectively. These values were comparable to the usual heat cured MMA/PMMA resins. In the heat cured resins, the amount of residual monomer was the lowest; less than 0.1%, even in the resin consisting of 50 wt% polymer. Thus, we prepared new acrylic resins with much less residual monomer than the usual MMA/PMMA resins. PMID:2491165

  8. Synthesis and Characterizations of Melamine-Based Epoxy Resins

    PubMed Central

    Ricciotti, Laura; Roviello, Giuseppina; Tarallo, Oreste; Borbone, Fabio; Ferone, Claudio; Colangelo, Francesco; Catauro, Michelina; Cioffi, Raffaele

    2013-01-01

    A new, easy and cost-effective synthetic procedure for the preparation of thermosetting melamine-based epoxy resins is reported. By this innovative synthetic method, different kinds of resins can be obtained just by mixing the reagents in the presence of a catalyst without solvent and with mild curing conditions. Two types of resins were synthesized using melamine and a glycidyl derivative (resins I) or by adding a silane derivative (resin II). The resins were characterized by means of chemical-physical and thermal techniques. Experimental results show that all the prepared resins have a good thermal stability, but differ for their mechanical properties: resin I exhibits remarkable stiffness with a storage modulus value up to 830 MPa at room temperature, while lower storage moduli were found for resin II, indicating that the presence of silane groups could enhance the flexibility of these materials. The resins show a pot life higher than 30 min, which makes these resins good candidates for practical applications. The functionalization with silane terminations can be exploited in the formulation of hybrid organic-inorganic composite materials. PMID:24013372

  9. Commercial Ion Exchange Resin Vitrification in Borosilicate Glass

    SciTech Connect

    Cicero-Herman, C.A.; Workman, P.; Poole, K.; Erich, D.; Harden, J.

    1998-05-01

    Bench-scale studies were performed to determine the feasibility of vitrification treatment of six resins representative of those used in the commercial nuclear industry. Each resin was successfully immobilized using the same proprietary borosilicate glass formulation. Waste loadings varied from 38 to 70 g of resin/100 g of glass produced depending on the particular resin, with volume reductions of 28 percent to 68 percent. The bench-scale results were used to perform a melter demonstration with one of the resins at the Clemson Environmental Technologies Laboratory (CETL). The resin used was a weakly acidic meth acrylic cation exchange resin. The vitrification process utilized represented a approximately 64 percent volume reduction. Glass characterization, radionuclide retention, offgas analyses, and system compatibility results will be discussed in this paper.

  10. Study on the resin temperature developments during UV imprinting process.

    PubMed

    Jeon, Jongduk; Jang, Siyoul

    2012-02-01

    During the imprinting process, the temperature of the UV resin increases as the phase of the resin changes from fluid into solid. During UV curing, some amount of heat is released from inside the resin and transferred into contacting materials. The heat flow is measured with photo-DSC, and other related thermal and mechanical properties of the resin. With the measured material properties, the temperature developments both inside of the resin layer and along the interfaces of the contacting materials are computed. During the UV exposure period, the thermal deformation of the mold, which directly influences the pattern distortion are investigated. Under this condition, the developments of strain and temperature inside the mold structure including the UV resin of 3-D shape are computed with the transient time scale during UV curing according to the thickness of resin layer. These computational results are expected to provide useful information for better designs of the imprinting mold and the process condition. PMID:22629908

  11. Electrically conductive resinous bond and method of manufacture

    DOEpatents

    Snowden, Jr., Thomas M.; Wells, Barbara J.

    1987-01-01

    A method of bonding elements together with a bond of high strength and good electrical conductivity which comprises: applying an unfilled polyimide resin between surfaces of the elements to be bonded, heat treating said unfilled polyimide resin in stages between a temperature range of about 40.degree. to 365.degree. C. to form a strong adhesive bond between said elements, applying a metal-filled polyimide resin overcoat between said elements so as to provide electrical connection therebetween, and heat treating said metal-filled polyimide resin with substantially the same temperature profile as the unfilled polyimide resin. The present invention is also concerned with an adhesive, resilient, substantially void free bonding combination for providing a high strength, electrically conductive adhesive attachment between electrically conductive elements which comprises a major amount of an unfilled polyimide resin and a minor amount of a metal-filled polyimide resin.

  12. Electrically conductive resinous bond and method of manufacture

    DOEpatents

    Snowden, T.M. Jr.; Wells, B.J.

    1985-01-01

    A method of bonding elements together with a bond of high strength and good electrical conductivity which comprises: applying an unfilled polyimide resin between surfaces of the elements to be bonded, heat treating said unfilled polyimide resin in stages between a temperature range of about 40 to 365/sup 0/C to form a strong adhesive bond between said elements, applying a metal-filled polyimide resin overcoat between said elements so as to provide electrical connection therebetween, and heat treating said metal-filled polyimide resin with substantially the same temperature profile as the unfilled polyimide resin. The present invention is also concerned with an adhesive, resilient, substantially void free bonding combination for providing a high strength, electrically conductive adhesive attachment between electrically conductive elements which comprises a major amount of an unfilled polyimide resin and a minor amount of a metal-filled polyimide resin.

  13. Flammability of Epoxy Resins Containing Phosphorus

    NASA Technical Reports Server (NTRS)

    Hergenrother, P. M.; Thompson, C. M.; Smith, J. G.; Connell, J. W.; Hinkley, J. A.

    2005-01-01

    As part of a program to develop fire-resistant exterior composite structures for future subsonic commercial and general aviation aircraft, flame-retardant epoxy resins are under investigation. Epoxies and their curing agents (aromatic diamines) containing phosphorus were synthesized and used to prepare epoxy formulations. Phosphorus was incorporated within the backbone of the epoxy resin and not used as an additive. The resulting cured neat epoxy formulations were characterized by thermogravimetric analysis, propane torch test, elemental analysis, microscale combustion calorimetry, and fire calorimetry. Several formulations showed excellent flame retardation with phosphorous contents as low as 1.5% by weight. The fracture toughness and compressive strength of several cured formulations showed no detrimental effect due to phosphorus content. The chemistry and properties of these new epoxy formulations are discussed.

  14. Ethynylated aromatics as high temperature matrix resins

    NASA Technical Reports Server (NTRS)

    Hurwitz, F. I.

    1987-01-01

    Difunctional and trifunctional arylacetylenes were used as monomers to form thermoset matrix resin composites. Composites can be hot-pressed at 180 C to react 80 percent of the acetylene groups. Crosslinking is completed by postcuring at 350 C. The postcured resins are thermally stable to nominally 460 C in air. As a result of their high crosslink density, the matrix exhibits brittle failure when uniaxial composites are tested in tension. Failure of both uniaixial tensile and flexural specimens occurs in shear at the fiber-matrix interface. Tensile fracture stresses for 0-deg composites fabricated with 60 v/o Celion 6K graphite fiber were 827 MPa. The strain to failure was 0.5 percent. Composites fabricated with 8 harness satin Celion cloth (Fiberite 1133) and tested in tension also failed in shear at tensile stresses of 413 MPa.

  15. Epoxy resins in the construction industry.

    PubMed

    Spee, Ton; Van Duivenbooden, Cor; Terwoert, Jeroen

    2006-09-01

    Epoxy resins are used as coatings, adhesives, and in wood and concrete repair. However, epoxy resins can be highly irritating to the skin and are strong sensitizers. Some hardeners are carcinogenic. Based on the results of earlier Dutch studies, an international project on "best practices,"--Epoxy Code--with epoxy products was started. Partners were from Denmark, Germany, the Netherlands, and the UK. The "Code" deals with substitution, safe working procedures, safer tools, and skin protection. The feasibility of an internationally agreed "ranking system" for the health risks of epoxy products was studied. Such a ranking system should inform the user of the harmfulness of different epoxies and stimulate research on less harmful products by product developers. PMID:17119222

  16. Ethynylated aromatics as high temperature matrix resins

    NASA Technical Reports Server (NTRS)

    Hurwitz, Frances I.

    1986-01-01

    Difunctional and trifunctional arylacetylenes were used as monomers to form thermoset matrix resin composites. Composites can be hot pressed at 180 C to react 80 percent of the acetylene groups. Crosslinking is completed by postcuring at 350 C. The postcured resins are thermally stable to nominally 460 C in air. As a result of their high crosslink density, the matrix exhibits brittle failure when unaxial composites are tested in tension. Failure of both uniaxial tensile and flexural specimens occurs in shear at the fiber matrix interface. Tensile fracture stresses for 0 deg composites fabricated with 60 v/o Celion 6K graphite fiber were 827 MPa. The strain to failure was 0.5 percent. Composites fabricated with 8 harness satin Celion cloth (Fiberite 1133) and tested in tension also failed in shear at tensile stresses of 413 MPa.

  17. Development of a Heterogeneous Laminating Resin

    NASA Technical Reports Server (NTRS)

    Gosnell, R.

    1984-01-01

    The feasibility of toughening the common types of matrix resins such as Narmco 5208 by utilizing a heterogeneous additive was examined. Some basic concepts and principles in the toughening of matrix resins for advanced composites were studied. The following conclusions were advanced: (1) the use of damage volume as a guide for measurement of impact resistance appears to be a valid determination; (2) short beam shear is a good test to determine the effect of toughening agents on mechanical properties; (3) rubber toughening results in improved laminate impact strength, but with substantial loss in high temperature dry and wet strength; (4) in the all-epoxy systems, the polycarbonate toughening agent seemed to be the most effective, although hot-wet strength is sacrificed; ABS was not as effective; and (5) in general, the toughened all-epoxy systems showed better damage tolerance, but less hot-wet strength; toughened bismaleimides had better hot-wet strength.

  18. Composites with improved fiber-resin interfacial adhesion

    NASA Technical Reports Server (NTRS)

    Cizmecioglu, Muzaffer (Inventor)

    1989-01-01

    The adhesion of fiber reinforcement such as high modulus graphite to a matrix resin such as polycarbonate is greatly enhanced by applying a very thin layer, suitably from 50 Angstroms to below 1000 Angstroms, to the surface of the fiber such as by immersing the fiber in a dilute solution of the matrix resin in a volatile solvent followed by draining to remove excess solution and air drying to remove the solvent. The thin layer wets the fiber surface. The very dilute solution of matrix resin is able to impregnate multifilament fibers and the solution evenly flows onto the surface of the fibers. A thin uniform layer is formed on the surface of the fiber after removal of the solvent. The matrix resin coated fiber is completely wetted by the matrix resin during formation of the composite. Increased adhesion of the resin to the fibers is observed at fracture. At least 65 percent of the surface of the graphite fiber is covered with polycarbonate resin at fracture whereas uncoated fibers have very little matrix resin adhering to their surfaces at fracture and epoxy sized graphite fibers exhibit only slightly higher coverage with matrix resin at fracture. Flexural modulus of the composite containing matrix resin coated fibers is increased by 50 percent and flexural strength by 37 percent as compared to composites made with unsized fibers.

  19. Anion-exchange resin-based desulfurization process. Final report

    SciTech Connect

    Sheth, A C; Dharmapurikar, R; Strevel, S D

    1994-01-01

    The following investigations were performed: (1) batch mode screening of eleven(11) commercially available resins and selection of three candidate resins for further evaluation in a fixed-bed setup. (2) Process variables study using three candidate resins in the fixed-bed setup and selection of the ``best`` resin for process economics development. (3) Exhaustion efficiency and solution concentration were found to be inversely related necessitating a trade-off between the resin cost versus the cost of evaporation/concentration of ensuing effluents. (4) Higher concentration of the HCO{sub 3}{sup {minus}} form of active sites over less active CO{sub 3}{sup 2{minus}} form of sites in the resin was believed to be the main reason for the observed increase in the equilibrium capacity of the resin at an elevated static CO{sub 2}-pressure. This Increase in capacity was found to level off around 80--120 psig range. The increase in CO{sub 2}-pressure, however, did not appear to affect the overall ion-exchange kinetics. (5) In the fixed-bed mode, the solution concentration was found to affect the equilibrium capacity of candidate resins. Their relationship was well satisfied by the Langmuir type non-linear equilibrium isotherm. Alternatively, the effect of solution concentration on overall ion-exchange kinetics varied from resin to resin. (6) Product inhibition effect on the resin was observed as an initial increase followed by a significant decrease in the resin`s equilibrium capacity for SO{sub 4}{sup 2{minus}} as the HCO{sub 3}{sup {minus}}/SO{sub 4}{sup 2{minus}} molar ratio in the solution was increased from 0 to 1.0. This ratio, however, did not affect the overall ion-exchange kinetics.

  20. Potential contribution of exposed resin to ecosystem emissions of monoterpenes

    NASA Astrophysics Data System (ADS)

    Eller, Allyson S. D.; Harley, Peter; Monson, Russell K.

    2013-10-01

    Conifers, especially pines, produce and store under pressure monoterpene-laden resin in canals located throughout the plant. When the plants are damaged and resin canals punctured, the resin is exuded and the monoterpenes are released into the atmosphere, a process that has been shown to influence ecosystem-level monoterpene emissions. Less attention has been paid to the small amounts of resin that are exuded from branches, expanding needles, developing pollen cones, and terminal buds in the absence of any damage. The goal of this study was to provide the first estimate of the potential of this naturally-exposed resin to influence emissions of monoterpenes from ponderosa pine (Pinus ponderosa) ecosystems. When resin is first exuded as small spherical beads from undamaged tissues it emits monoterpenes to the atmosphere at a rate that is four orders of magnitude greater than needle tissue with an equivalent exposed surface area and the emissions from exuded beads decline exponentially as the resin dries. We made measurements of resin beads on the branches of ponderosa pine trees in the middle of the growing season and found, on average, 0.15 cm2 of exposed resin bead surface area and 1250 cm2 of total needle surface area per branch tip. If the resin emerged over the course of 10 days, resin emissions would make up 10% of the ecosystem emissions each day. Since we only accounted for exposed resin at a single point in time, this is probably an underestimate of how much total resin is exuded from undamaged pine tissues over the course of a growing season. Our observations, however, reveal the importance of this previously unrecognized source of monoterpenes emitted from pine forests and its potential to influence regional atmospheric chemistry dynamics.

  1. Model-based rational strategy for chromatographic resin selection.

    PubMed

    Nfor, Beckley K; Zuluaga, Diego S; Verheijen, Peter J T; Verhaert, Peter D E M; van der Wielen, Luuk A M; Ottens, Marcel

    2011-01-01

    A model-based rational strategy for the selection of chromatographic resins is presented. The main question being addressed is that of selecting the most optimal chromatographic resin from a few promising alternatives. The methodology starts with chromatographic modeling,parameters acquisition, and model validation, followed by model-based optimization of the chromatographic separation for the resins of interest. Finally, the resins are rationally evaluated based on their optimized operating conditions and performance metrics such as product purity, yield, concentration, throughput, productivity, and cost. Resin evaluation proceeds by two main approaches. In the first approach, Pareto frontiers from multi-objective optimization of conflicting objectives are overlaid for different resins, enabling direct visualization and comparison of resin performances based on the feasible solution space. The second approach involves the transformation of the resin performances into weighted resin scores, enabling the simultaneous consideration of multiple performance metrics and the setting of priorities. The proposed model-based resin selection strategy was illustrated by evaluating three mixed mode adsorbents (ADH, PPA, and HEA) for the separation of a ternary mixture of bovine serum albumin, ovalbumin, and amyloglucosidase. In order of decreasing weighted resin score or performance, the top three resins for this separation were ADH [PPA[HEA. The proposed model-based approach could be a suitable alternative to column scouting during process development, the main strengths being that minimal experimentation is required and resins are evaluated under their ideal working conditions, enabling a fair comparison. This work also demonstrates the application of column modeling and optimization to mixed mode chromatography. PMID:22238769

  2. Mechanistic understanding of fouling of protein A chromatography resin.

    PubMed

    Pathak, Mili; Rathore, Anurag S

    2016-08-12

    This paper aims to provide a thorough understanding of how fouling of Protein A resin takes place. Binding and mass transport properties of widely used agarose-based Protein A resin, MabSelect SuRe™, have been examined to understand the mechanism of resin fouling. There could be various factors that impact resin fouling. These include product/impurity build-up due to components in the feed material and ligand degradation due to the use of harsh buffers. To unravel their contributions, cycling studies were performed with and without product loading. The results presented in this paper provide a lucid understanding of the causative factors that limit Protein A chromatographic resin lifetime. The capacity fall for protein A resin at the end of 100th cycle due to use of feed material was found to be five times greater than that without using feed material. Compared to the fresh resin, the cycled resin samples shows 24% reduction in particle porosity and 51% reduction in pore mass transfer coefficient. Transmission electron microscopy (TEM) was used to qualitatively monitor accumulation of foulants on the cycled resin. Fouled resin sample contained a dense residue in the interior and exterior of resin particle both as a film at the bead surface and as granules. The surface activation energy increased five times in the case of fouled resin sample. The major event in fouling was identified as the non-specific adsorption of the feed material components on resin, signaling that pore diffusion is the rate limiting step. It is anticipated that these findings will assist in development of a more robust and economical downstream manufacturing process for monoclonal antibody purification. PMID:27423774

  3. The effect of resin shades on microhardness, polymerization shrinkage, and color change of dental composite resins.

    PubMed

    Jeong, Tae-Sung; Kang, Ho-Seung; Kim, Sung-Ki; Kim, Shin; Kim, Hyung-Il; Kwon, Yong Hoon

    2009-07-01

    The present study sought to evaluate the effect of resin shades on the degree of the polymerization. To this end, response variables affected by the degree of polymerization were examined in this study - namely, microhardness, polymerization shrinkage, and color change. Two commercial composite resins of four different shades were employed in this study: shades A3, A3.5, B3, and C3 of Z250 (Z2) and shades A3, A3.5, B3, and B4 of Solitaire 2 (S2). After light curing, the reflectance/absorbance, microhardness, polymerization shrinkage, and color change of the specimens were measured. On reflectance and absorbance, Z2 and S2 showed similar distribution curves regardless of the resin shade, with shade A3.5 of Z2 and shade A3 of S2 exhibiting the lowest/highest distributions. Similarly for attenuation coefficient and microhardness, the lowest/highest values were exhibited by shade A3.5 of Z2 and shade A3 of S2. On polymerization shrinkage, no statistically significant differences were observed among the different shades of Z2. Similarly for color change, Z2 specimens exhibited only a slight (DeltaE*=0.5-0.9) color change after immersion in distilled water for 10 days, except for shades A3 and A3.5. Taken together, results of the present study suggested that the degree of polymerization of the tested composite resins was minimally affected by resin shade. PMID:19721281

  4. 21 CFR 177.1500 - Nylon resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    .... Nylon 6/69 resins for use only as specified in 21 CFR 177.1395 of this chapter 1.09±0.02 270-277 >140..., see the List of CFR Sections Affected, which appears in the Finding Aids section of the printed volume... apparatus. The use of crossed nicol prisms with a microscope hot stage and reading of the thermometer...

  5. 21 CFR 177.1500 - Nylon resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    .... Nylon 6/69 resins for use only as specified in 21 CFR 177.1395 of this chapter 1.09±0.02 270-277 >140..., see the List of CFR Sections Affected, which appears in the Finding Aids section of the printed volume... apparatus. The use of crossed nicol prisms with a microscope hot stage and reading of the thermometer...

  6. 21 CFR 177.1500 - Nylon resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    .... Nylon 6/69 resins for use only as specified in 21 CFR 177.1395 of this chapter 1.09±0.02 270-277 >140..., see the List of CFR Sections Affected, which appears in the Finding Aids section of the printed volume... apparatus. The use of crossed nicol prisms with a microscope hot stage and reading of the thermometer...

  7. Single Frequency Characterization of a Commercial Resin

    SciTech Connect

    Sauers, Isidor; Tuncer, Enis; Polizos, Georgios; James, David Randy; Ellis, Alvin R; Pace, Marshall O

    2009-10-01

    Electrical impedance measurement methods are extensively utilized to characterize dielectric materials. There are not many inexpensive commercially available measurement systems for low frequencies. In this paper an impedance measurement method using an electrometer is presented. The method can be employed for frequencies lower than 100 mHz. To illustrate the usefulness of the presented method, an epoxy resin is characterized and the influence of thermal aging is investigated.

  8. 21 CFR 177.1500 - Nylon resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    .... Nylon 6/69 resins for use only as specified in 21 CFR 177.1395 of this chapter 1.09±0.02 270-277 >140... approximately the size of the molding powder. This can be done conveniently by using a small-scale commercial... while still hot, using a Buchner funnel approximately 5 inches in diameter, a suction flask, and...

  9. Ceramic whisker reinforcement of dental resin composites.

    PubMed

    Xu, H H; Martin, T A; Antonucci, J M; Eichmiller, F C

    1999-02-01

    Resin composites currently available are not suitable for use as large stress-bearing posterior restorations involving cusps due to their tendencies toward excessive fracture and wear. The glass fillers in composites provide only limited reinforcement because of the brittleness and low strength of glass. The aim of the present study was to reinforce dental resins with ceramic single-crystalline whiskers of elongated shapes that possess extremely high strength. A novel method was developed that consisted of fusing silicate glass particles onto the surfaces of individual whiskers for a two-fold benefit: (1) to facilitate silanization regardless of whisker composition; and (2) to enhance whisker retention in the matrix by providing rougher whisker surfaces. Silicon nitride whiskers, with an average diameter of 0.4 microm and length of 5 microm, were coated by the fusion of silica particles 0.04 microm in size to the whisker surface at temperatures ranging from 650 degrees C to 1000 degrees C. The coated whiskers were silanized and manually blended with resins by spatulation. Flexural, fracture toughness, and indentation tests were carried out for evaluation of the properties of the whisker-reinforced composites in comparison with conventional composites. A two-fold increase in strength and toughness was achieved in the whisker-reinforced composite, together with a substantially enhanced resistance to contact damage and microcracking. The highest flexural strength (195+/-8 MPa) and fracture toughness (2.1+/-0.3 MPa x m(1/2)) occurred in a composite reinforced with a whisker-silica mixture at whisker:silica mass ratio of 2:1 fused at 800 degrees C. To conclude, the strength, toughness, and contact damage resistance of dental resin composites can be substantially improved by reinforcement with fillers of ceramic whiskers fused with silica glass particles. PMID:10029470

  10. Ethynyl terminated imidothioethers and resins therefrom

    NASA Technical Reports Server (NTRS)

    Hergenrother, Paul M. (Inventor); Connell, John W. (Inventor); Bass, R. Gerald (Inventor)

    1991-01-01

    Ethynyl terminated imidothioethers (ETIs) are prepared by the reaction of a dimercaptan, such as 4,4'-dimercaptodiphenyl ether, and an ethynyl containing maleimide, such as N-(3-ethynylphenyl)maleimide. Blends of these ETIs and ethynyl terminated polymeric materials, such as ethynyl terminated sulfones and ethynyl terminated arylene ethers, are also prepared. These resin blends exhibit excellent processability, and the cured blends show excellent fracture toughness and solvent resistance, as well as excellent adhesive and composite properties.

  11. Chemoviscosity modeling for thermosetting resin systems, 4

    NASA Technical Reports Server (NTRS)

    Hou, T. H.; Huang, Joan Y. Z.

    1989-01-01

    An experimental study on the changes of chemorheological properties has been conducted and analyzed on commercial Hercules 3501-6 resin system cured under several isothermal conditions between 375 and 435 K. For the cure temperatures equal to or greater than 385 K, the storage modulus curing curves, G prime (t), exhibited abrupt changes in slope which occurred at various times depending on the curing temperatures and were attributed to the onset of gelation reactions. The crossover points between G prime (t) and G double prime (t) curves were observed for curing temperatures equal to or greater than 400 K. The gelation and the crossover points obtained from the chemorheological measurements, therefore, defined two characteristic resin states during cure. Approximately the same value for the degree of cure was reached by the advancement of the reaction at each of these states. The temperature dependency of the viscosities for the characteristic resin states and the rate constants of increase in moduli at different stages of curing were analyzed. Various G prime (t) and G double prime (t) isothermal curing curves were also shown to be capable of being superimposed on one another by the principle of time-temperature superposition. The resultant shift factors a sub t(t) and a Eta(T) were shown to follow the Arrhenius type relationship. Values of the activation energy suggested that the reaction kinetics, instead of the diffusion mechanism, was the limiting step in the overall resin advancement for the cure at temperatures equal to or greater than 385 K.

  12. Processable polyimide adhesive and matrix composite resin

    NASA Technical Reports Server (NTRS)

    Pratt, J. Richard (Inventor); St.clair, Terry L. (Inventor); Progar, Donald J. (Inventor)

    1990-01-01

    A high temperature polyimide composition prepared by reacting 4,4'-isophthaloyldiphthalic anhydride with metaphenylenediamine is employed to prepare matrix resins, adhesives, films, coatings, moldings, and laminates, especially those showing enhanced flow with retention of mechanical and adhesive properties. It can be used in the aerospace industry, for example, in joining metals to metals or metals to composite structures. One area of application is in the manufacture of lighter and stronger aircraft and spacecraft structures.

  13. Kinetic modelling of vinyl ester resin polymerization

    SciTech Connect

    Dhulipala, R.; Kreig. G.; Hawley, M.C.

    1993-12-31

    The study of kinetics offers a substantional incentive in the endeavor to manufacture polymer matrix composites at high speeds. The study enables one to optimize the curing cycle based on the specific curing characteristics of the resin and also makes it possible to simulate the curing process. This paper reports the results of the modelling of the thermal curing of the vinyl ester resin. The parameters for the proposed model have been calculated based on conversion-vs-data generated at various temperatures and Benzoyl peroxide (initiator) concentrations. The extent of cure of the resin mixture was determined using Fourier Transform Infrared Spectroscopy. In this model the termination rate constant is considered to drop with extent of cure until a limiting value is reached. The limiting value is a consequence of the active chain ends possessing a degree of mobility due to the propagation reaction even though the translational motion of the growing for radicals in increasingly restricted with conversion. Good agreements is observed between the model predictions and the experimental data.

  14. Composite fabrication via resin transfer molding technology

    SciTech Connect

    Jamison, G.M.; Domeier, L.A.

    1996-04-01

    The IMPReS (Integrated Modeling and Processing of Resin-based Structures) Program was funded in FY95 to consolidate, evaluate and enhance Sandia`s capabilities in the design and fabrication of composite structures. A key driver of this and related programs was the need for more agile product development processes and for model based design and fabrication tools across all of Sandia`s material technologies. A team of polymer, composite and modeling personnel was assembled to benchmark Sandia`s existing expertise in this area relative to industrial and academic programs and to initiate the tasks required to meet Sandia`s future needs. RTM (Resin Transfer Molding) was selected as the focus composite fabrication technology due to its versatility and growing use in industry. Modeling efforts focused on the prediction of composite mechanical properties and failure/damage mechanisms and also on the uncured resin flow processes typical of RTM. Appropriate molds and test composites were fabricated and model validation studies begun. This report summarizes and archives the modeling and fabrication studies carried out under IMPReS and evaluates the status of composite technology within Sandia. It should provide a complete and convenient baseline for future composite technology efforts within Sandia.

  15. Chemoviscosity modeling for thermosetting resins - I

    NASA Technical Reports Server (NTRS)

    Hou, T. H.

    1984-01-01

    A new analytical model for chemoviscosity variation during cure of thermosetting resins was developed. This model is derived by modifying the widely used WLF (Williams-Landel-Ferry) Theory in polymer rheology. Major assumptions involved are that the rate of reaction is diffusion controlled and is linearly inversely proportional to the viscosity of the medium over the entire cure cycle. The resultant first order nonlinear differential equation is solved numerically, and the model predictions compare favorably with experimental data of EPON 828/Agent U obtained on a Rheometrics System 4 Rheometer. The model describes chemoviscosity up to a range of six orders of magnitude under isothermal curing conditions. The extremely non-linear chemoviscosity profile for a dynamic heating cure cycle is predicted as well. The model is also shown to predict changes of glass transition temperature for the thermosetting resin during cure. The physical significance of this prediction is unclear at the present time, however, and further research is required. From the chemoviscosity simulation point of view, the technique of establishing an analytical model as described here is easily applied to any thermosetting resin. The model thus obtained is used in real-time process controls for fabricating composite materials.

  16. Morphological characterization of furfuraldehyde resins adsorbents

    SciTech Connect

    Sanchez, R.; Monteiro, S.N.; D`Almeida, J.R.

    1996-12-31

    Sugar cane is one of the most traditional plantation cultivated crops in large areas in Brazil. The State University of the North of Rio de Janeiro, UENF, is currently engaged in a program aimed to exploit the potentialities of sugar cane industry as a self sustained non-polluting enterprise. One of the projects being carried out at the UENF is the transformation of sugar cane bagasse in precursor materials for the industry of furan derivatives such as the furfuraldehyde resins obtained by acid catalysis. The possibility of employing acid catalyzed furfuraldehyde resins as selective adsorbents has arisen during a comprehensive study of physical-chemical adsorption properties of these materials. The morphology of these resins depend on the synthesis method. Scanning Electron Microscopic studies of these materials which were synthesized, in bulk (FH-M) and solution (FH-D), showed differences in surface density and particle size. Using mercury porosimeter techniques and BET adsorption methods, it was found different pore size distributions and a decrement in surface area when solvent was employed in the synthesis process. By thermogravimetric analysis it was found similar weight losses (6%) of water adsorption and a small differences in thermal stabilities.

  17. Surface integrity of provisional resin materials

    NASA Astrophysics Data System (ADS)

    Abouelatta, O. B.; El-Bediwi, A.; Sakrana, A.; Jiang, X. Q.; Blunt, L.

    2006-03-01

    Provisional resin materials are widely used in prosthetic dentistry and play an important role in the success of restorative treatment. Therefore, these materials must meet the requirements of preserving surface integrity during the treatment process. This study was done to evaluate surface roughness and microhardness of two provisional resin materials after 37 °C water storage. Two rectangular samples 21 mm × 11 mm × 3 mm, one bis-acrylic (bis-acrylic-Protemp II) and one polyethyl methacrylate (Trim®-PEMA) were fabricated as examples of provisional materials (n = 5 per material). The specimens were stored in 37 °C deionized distilled water for 24 h, 1, 2 and 3 weeks. The control specimens were not stored in water. The surface roughness of the tested materials (n = 10) was measured using a profilometer. Microhardness tests were conducted using a Vickers microscope mounted indenter system (n = 10). At 24 h, the surface roughness was recorded with bis-acrylic-Protemp II as higher than methacrylate materials. No significant differences of microhardness between Trim®-PEMA and bis-acrylic-Protemp II were recognized at 1, 2 and 3 weeks. The microhardness values increased with the increase of surface roughness and vice versa in both Trim®-PEMA and bis-acrylic-Protemp II. Both surface roughness and microhardness are affected by water storage. Bis-acrylic-Protemp II revealed better results in hardness than methacrylate resins, whereas Trim®-PEMA has a better surface roughness.

  18. Correlations of norbornenyl crosslinked polyimide resin structures with resin thermo-oxidative stability, resin glass transition temperature and composite initial mechanical properties

    NASA Technical Reports Server (NTRS)

    Alston, William B.

    1988-01-01

    PMR (polymerization of monomeric reactants) methodology was used to prepare 70 different polyimide oligomeric resins and 30 different unidirectional graphite fiber/polyimide composites. Monomeric composition as well as chain length between sites of crosslinks were varied to examine their effects on resin thermo-oxidative stability and glass transition temperature (Tg) of the cured/postcured resins. A linear correlation of decreasing 316 C resin weight loss/surface area versus (1) decreasing aliphatic content, or (2) increasing benzylic/aliphatic content stoichiometry ratio over a wide range of resin compositions was observed. An almost linear correlation of Tg versus molecular distance between the crosslinks was also observed. An attempt was made to correlate Tg with initial composite mechanical properties (flexural strength and interlaminar shear strength). However, the scatter in mechanical strength data prevented obtaining a clear correlation. Instead, only a range of composite mechanical properties was obtained at 25, 288, and 316 C. Perhaps more importantly, what did become apparent during the correlation study was (1) the PMR methodology could be used to prepare composites from resins containing a wide variety of monomer modifications, (2) that these composites almost invariably provided satisfactory initial mechanical properties as long as the resins formulated exhibited satisfactory processing flow, and (3) that PMR resins exhibited predictable rates of 316 C weight loss/surface area based on their benzylic/aliphatic stoichiometery ratio.

  19. CHARACTERIZATION OF CYCLED SPHERICAL RESORCINOL-FORMALDEHYDE ION EXCHANGE RESIN

    SciTech Connect

    Nash, C.; Duignan, M.

    2010-02-23

    This report presents characterization data for two spherical resorcinol-formaldehyde (sRF) resin beds that had processed cesium in non-radioactive and radioactive cycles. All column cycle operations for the resin beds including loading, displacements, elution, regeneration, breakthroughs, and solution analyses are reported in Nash and Duignan, 2009a. That report covered four ion exchange (IX) campaigns using the two {approx}11 mL beds in columns in a lead-lag arrangement. The first two campaigns used Savannah River Site (SRS) Tank 2F nonradioactive simulant while the latter two were fed with actual dissolved salt in the Savannah River National Laboratory (SRNL) Shielded Cells. Both radioactive cycles ran to cesium breakthrough of the lead column. The resin beds saw in excess of 400 bed volumes of feed in each cycle. Resin disposal plans in tank farm processing depend on characterizations of resin used with actual tank feed. Following a final 30 bed volume (BV) elution with nitric acid, the resin beds were found to contain detectable chromium, barium, boron, aluminum, iron, sodium, sulfur, plutonium, cesium, and mercury. Resin affinity for plutonium is important in criticality safety considerations. Cesium-137 was found to be less than 10E+7 dpm/g of resin, similar to past work with sRF resin. Sulfur levels are reasonably consistent with other work and are expected to represent sulfur chemistry used in the resin manufacture. There were low but detectable levels of technetium, americium, and curium. Toxicity Characteristic Leaching Procedure (TCLP) work on the used (eluted) resin samples showed significant contents of mercury, barium, and chromium. One resin sample exceeded the TCLP level for mercury while the other metals were below TCLP levels. TCLP organics measurements indicated measurable benzene in one case, though the source was unknown. Results of this work were compared with other work on similar sRF resin characterizations in this report. This is the first

  20. Modification of unsaturated polyester resins (UP) and reinforced UP resins via plasma treatment

    NASA Astrophysics Data System (ADS)

    Li, Guanglu; Wei, Xing; Wang, Wanjun; He, Tao; Li, Xuemei

    2010-10-01

    Unsaturated polyester resins (UP) and reinforced composite unsaturated polyester resins (RCP) were made superhydrophobic by plasma assisted methods. Both CF 4-plasma-enhanced chemical vapor deposition (CF 4-PECVD) and alternative method were tested. The surfaces were characterized by water contact angle (CA) measurements and scanning electron microscopy (SEM). Water contact angle results indicated that CF 4-PECVD can significantly improve the wettability of UP surfaces, but suffer from difficulties for RCP surfaces. Alternatively, O 2 plasma followed by self-assembly of octadecyltrichlorosilane (OTS) self-assembled monolayer (SAM) was tested. It was shown that regardless of the filler percentage, O 2 plasma followed by self-assembly of OTS monolayer formation all led to superhydrophobic surfaces. The results provided a means to improve the wettability of reinforced UP resins (RCP).

  1. Machine for applying a two component resin to a roadway surface

    DOEpatents

    Huszagh, D.W.

    1984-01-01

    A portable machine for spraying two component resins onto a roadway, the machine having a pneumatic control system, including means for purging the machine of mixed resin with air and then removing remaining resin with solvent. Interlocks prevent contamination of solvent and resin, and mixed resin can be purged in the event of a power failure.

  2. 21 CFR 175.320 - Resinous and polymeric coatings for polyolefin films.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... of the total coating solids. Polyamide resins (CAS Reg. No. 68139-70-8), as the basic resin, derived... polyamide resin Ethylenediamine (CAS Reg. No. 107-15-3) Piperazine (CAS Reg. No. 110-85-0) in an amount not to exceed 6.4 percent by weight of the polyamide resin Polyamide resins, derived from...

  3. 21 CFR 175.320 - Resinous and polymeric coatings for polyolefin films.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... of the total coating solids. Polyamide resins (CAS Reg. No. 68139-70-8), as the basic resin, derived... polyamide resin Ethylenediamine (CAS Reg. No. 107-15-3) Piperazine (CAS Reg. No. 110-85-0) in an amount not to exceed 6.4 percent by weight of the polyamide resin Polyamide resins, derived from...

  4. Machine for applying a two component resin to a roadway surface

    DOEpatents

    Huszagh, Donald W.

    1985-01-01

    A portable machine for spraying two component resins onto a roadway, the machine having a pneumatic control system, including apparatus for purging the machine of mixed resin with air and then removing remaining resin with solvent. Interlocks prevent contamination of solvent and resin, and mixed resin can be purged in the event of a power failure.

  5. Kinetic study of metal biosorption to a brown alga, Kjellmaniella crassiforia.

    PubMed

    Seki, Hideshi; Suzuki, Akira

    2002-02-15

    A kinetic study of cadmium and lead biosorption to a brown alga, Kjellmaniella crassiforia, was carried out. The shrinking core model derived by M. Gopala Rao and A. K. Gupta (Chem. Eng. J.24, 181, (1982)) was modified and adapted for description of the rate process of cadmium and lead biosorption to the alga. The biosorption rate process was well described and average apparent diffusion coefficient of about 9 x 10(-6) cm(2) s(-1) was found for both cadmium and lead ions. The value was 20 to 50 times higher than the apparent diffusion coefficients of cadmium and lead ions in strong-acid resins like Dowex 50W-X8. PMID:16290409

  6. Production and separation of Astatine Radionuclides: some new addition to Astatine Chemistry.

    PubMed

    Roy, Kamalika; Lahiri, Susanta

    2008-05-01

    For the first time no-carrier-added (nca) (209,210)At radionuclides were produced by heavy ion ((7)Li) activation from 4 mg/cm(2) lead nitrate target. Astatine was separated from the bulk target by three different approaches. Nca astatine radionuclide was selectively partitioned in the (i) polymer rich phase of an aqueous biphasic system consisting of polyethylene glycol (PEG) 4000 (50% w/w) and 2M Na(2)SO(4) solution (ii) aqueous phase of a liquid liquid extraction system being comprised of a liquid cation exchanger, HDEHP (di-2-ethylhexyl phosphoric acid) (0.5%) and liquor ammonia (iii) liquid phase of a solid liquid extraction system of cation exchange resin Dowex-50 and 10(-6)M HCl. Very high separation factors have been achieved in all the three methods. PMID:18222695

  7. Epoxy resin developments for large superconducting magnets impregnation

    NASA Astrophysics Data System (ADS)

    Rey, J. M.; Gallet, B.; Kircher, F.; Lottin, J. C.

    The future detectors ATLAS and CMS of the Large Hadron Collider at CERN will use two huge superconducting magnets. Both are now under design, and their electrical insulation could be realized using epoxy resin and a wet impregnation technique. Because of their large dimensions, and the indirect cooling of the superconductor, the strengths of the resin and of the resin/conductor interface are of major importance. A new generation of epoxy resins for vacuum/pressure impregnation methods has been tested, and compared with some classical and well-known epoxy resins used in impregnation techniques. In order to understand the mechanical behaviour at 4 K, the complete evolution from liquid state to low temperature service condition is considered. The paper will present some results on the mechanical properties, the density and the chemical shrinkage occurring during the polymerization and the thermal contraction between room temperature and 4 K for these different types of epoxy resins.

  8. Investigation on the electron-beam curing of vinylester resin

    NASA Astrophysics Data System (ADS)

    Xiancong, Huang; Meiwu, Shi; Guotai, Zhou; Hong, Zhou; Xiaopeng, Hao; Chunlan, Zhou

    2008-05-01

    A typical vinylester resin, Derakane 411-350, was electron-beam (EB) cured without initiators. The curing process was investigated by gel-fraction testing, FTIR and Raman spectroscopies. Both dynamic numerical analysis and positron annihilation life spectroscopy were utilized to analyze the microstructure of resin samples irradiated with different doses and dose rates. Resin irradiated with the same dose at a low dose rate achieved a higher degree of cure than those samples irradiated with a high dose rate. Resin irradiated with low dose rates had a lower free-volume fraction with smaller interstices and a more uniform microstructure. The glass-transition temperature of the resin increased with increasing irradiation dose. The mechanical properties of the EB-cured resin confirmed the analysis of changes in microstructure arising from irradiation.

  9. Solidification of ion exchange resin wastes in hydraulic cement

    SciTech Connect

    Neilson, R.M. Jr.; Kalb, P.; Fuhrmann, M.; Colombo, P.

    1982-01-01

    Work has been conducted to investigate the solidification of ion exchange resin wastes with portland cements. These efforts have been directed toward the development of acceptable formulations for the solidification of ion exchange resin wastes and the characterization of the resultant waste forms. This paper describes formulation development work and defines acceptable formulations in terms of ternary phase compositional diagrams. The effects of cement type, resin type, resin loading, waste/cement ratio and water/cement ratio are described. The leachability of unsolidified and solidified resin waste forms and its relationship to full-scale waste form behavior is discussed. Gamma irradiation was found to improve waste form integrity, apparently as a result of increased resin crosslinking. Modifications to improve waste form integrity are described. 3 tables.

  10. Inorganic resins for clinical use of .sup.213Bi generators

    DOEpatents

    DePaoli, David W.; Hu, Michael Z.; Mirzadeh, Saed; Clavier, John W.

    2011-03-29

    Applicant's invention is a radionuclide generator resin material for radiochemical separation of daughter radionuclides, particularly .sup.213Bi, from a solution of parental radionuclides, the resin material capable of providing clinical quantities of .sup.213Bi of at least 20-mCi, wherein the resin material comprises a silica-based structure having at least one bifunctional ligand covalently attached to the surface of the silica-based structure. The bifunctional ligand comprises a chemical group having desirable surface functionality to enable the covalent attachment of the bifunctional ligand thereon the surface of the structure and the bifunctional ligand further comprises a second chemical group capable of binding and holding the parental radionuclides on the resin material while allowing the daughter radionuclides to elute off the resin material. The bifunctional ligand has a carbon chain with a limited number of carbons to maintain radiation stability of the resin material.

  11. Bismaleimide resins for flame resistant honeycomb sandwich panels

    NASA Technical Reports Server (NTRS)

    Stenzenberger, H. D.

    1978-01-01

    Bismaleimide resins are prime candidates for nonflammable aircraft interior panels. Three resin types with different structures and processing characteristics were formulated. Resin M 751 was used to fabricate 100 kg of glass fabric prepregs which were used for the preparation of face sheets for honeycomb sandwich panels. Prepreg characteristics and curing cycles for laminate fabrication are provided. In order to advance beyond the current solvent resin technology for fibre and fabric impregnation, a hot melt solvent-less resin system was prepared and characterized. Preliminary tests were performed to develop a wet bonding process for the fabrication of advanced sandwich honeycomb panels by use of polybismaleimide glass fabric face sheets and polybismaleimide Nomex honeycomb core. B-stage material was used for both the core and the face sheet, providing flatwise tensile properties equivalent to those obtained by the state-of-the-art 3-step process which includes an epoxy adhesive resin.

  12. Do resin cements influence the cuspal deflection of teeth restored with composite resin inlays?

    PubMed

    da Rosa, Helen C V; Marcondes, Maurem L; de Souza, Niélli C; Weber, João B B; Spohr, Ana M

    2015-04-01

    The aim of this study was to evaluate the influence of different resin cements on the cuspal deflection of endodontically treated teeth restored with composite resin inlays. Sixty upper premolars were randomly divided into five groups (n=12): 1 - sound teeth; 2 - cavity; 3 - Rely X ARC; 4 - RelyX Unicem; 5 - SeT. The teeth from groups 2, 3, 4 and 5 received a MOD preparation and endodontic treatment. Impressions were made with vinyl polysiloxane and poured using type IV die stone in groups 3, 4 and 5. Inlays with composite resin were built over each cast and luted with the resin cements. A 200 N load was applied on the occlusal surface, and cuspal deflection was measured using a micrometer. After 24 h, cuspal deflection was measured again using a 300 N load. The Student t-test showed that there was no statistically significant difference between the 200 N and 300 N occlusal loads only for the sound teeth group (p = 0.389) and the RelyX ARC group (p = 0.188). ANOVA and Tukey'test showed that the sound teeth had the lowest mean cuspal deflection, differing statistically from the other groups (p<0.05). The highest cuspal deflections were obtained in the SeT group and the cavity group, with no statistical difference between them. Intermediate values were obtained in RelyX ARC group and RelyX Unicem group, which differed statistically. The self-adhesive resin cements RelyX Unicem and SeT showed less capacity to maintain the stiffness of the tooth/restoration complex than the conventional resin cement RelyX ARC. PMID:25950160

  13. Enhancing the Novolak resin resist resolution by adding phenol to fractionated resin

    NASA Astrophysics Data System (ADS)

    Sekiguchi, Atsushi; Matsumoto, Yoko; Tanaka, Hatsuyuki; Horiuchi, Toshiyuki; Sensu, Yoshihisa; Takei, Satoshi; Hanabata, Makoto

    2016-03-01

    Novolak resists have been widely used in IC production and are still used in the production of flat panel displays (FPDs) and MEMS. However, with the advent of high-definition products, FPDs increasingly face requirements for finer dimensions. These trends have generated requirements for higher sensitivity, higher resolution, and wider process margin for novolak resists. Using a lithography simulator with the goal of improving the performance of novolak resists, we examined various approaches to improving resist materials. This report discusses efforts to improve resolution and sensitivity using highly fractionated novolak resins and adding low molecular weight phenol resins.

  14. Chromium Ions Improve Moisure Resistance of Epoxy Resins

    NASA Technical Reports Server (NTRS)

    St. Clair, A. K.; St. Clair, T. L.; Stoakley, D. M.; Singh, J. J.; Sprinkle, D. R.

    1986-01-01

    Broad spectrum of thermosetting epoxy resins used on commercial and military aircraft, primarily as composite matrices and adhesives. In new technique, chromium-ion containing epoxy with improved resistance to moisture produced where chromium ions believed to prevent absorption of water molecules by coordinating themselves to hydroxyl groups on epoxy chain. Anticipated that improved epoxy formulation useful as composite matrix resin, adhesive, or casting resin for applications on commercial and advanced aircraft. Improvement made without sacrifice in mechanical properties of polymer.

  15. 21 CFR 173.25 - Ion-exchange resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...,” February 4, 1998, which is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ion-exchange resins. 173.25 Section 173.25 Food and... Substances and Polymer Adjuvants for Food Treatment § 173.25 Ion-exchange resins. Ion-exchange resins may...

  16. 21 CFR 173.25 - Ion-exchange resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...,” February 4, 1998, which is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ion-exchange resins. 173.25 Section 173.25 Food... for Food Treatment § 173.25 Ion-exchange resins. Ion-exchange resins may be safely used in...

  17. Internal stabilization of polycarbonate resins by two stage radiation process

    NASA Technical Reports Server (NTRS)

    Gupta, Amitava (Inventor); Liang, Ranty H. (Inventor); Yavrouian, Andre H. (Inventor)

    1988-01-01

    A new polycarbonate copolymer resin is formed by internal generation of stabilizers bound to the polymer chain. Irradiation of a solid piece or a deoxygenated solution of the resin at a first frequency below 300 nm generates 2 to 8 mol percent of phenyl salicylate groups which are rearranged to dihydroxybenzophenone groups by irradiating the resin under oxygen excluding conditions at a second frequency from 300 to 320 nm.

  18. High performance mixed bisimide resins and composites based thereon

    NASA Technical Reports Server (NTRS)

    Parker, J. A.; ations.

    1986-01-01

    Mixtures of bismaleimide/biscitraconirnide resins produces materials which have better handling, processing or mechanical and thermal properties, particularly in graphite composites, than materials made with the individual resins. The mechanical strength of cured graphite composites prepared from a 1:1 copolymer of such bisimide resins is excellent at both ambient and elevated temperatures. The copolymer mixture provides improved composites which are lighter than metals and replace metals in many aerospace applications.

  19. Hydrolyzable polyester resins, varnishes and coating compositions containing the same

    SciTech Connect

    Yamamori, Naoki; Yokoi, Junji; Yoshikawa, Motoyoshi

    1984-01-01

    Preparation of hydrolyzable polyester resin comprising reacting polycarboxylic acid and polyhydric alcohol components, which is characterized by using, as at least part of said polyhydric alcohol component, a metallic salt of hydroxy carboxylic acid of the formula defined and effecting the polycondensation at a temperature which is no more than the decomposition temperature of said metallic salt. The polyester resins are useful as resinous vehicle of varnishes and antifouling paints.

  20. Trace metal preconcentration using a thioglycolate chelating resin

    SciTech Connect

    Howard, A.G.; Danilona-Mirzaians, R.

    1989-01-01

    A styrene-divinyl benzene copolymer resin (Amberlite XAD-4), modified with thioglycolate complexing groups, has been employed for the preconcentration of cadmium, zinc, lead and nickel from natural waters. The resin exhibits its strongest affinity for cadmium and lead but can be used to quantitatively remove all four metals from non-saline waters. With seawater samples, the resin is best only employed for the enrichment of cadmium and lead as the recovery of nickel and zinc from this medium is poor.

  1. Mini fiberglass post for composite resin restorations: A clinical report.

    PubMed

    Morgan, Luís Fernando Dos Santos Alves; Martins, Adriana Vieira; Albuquerque, Rodrigo de Castro; Silveira, Rodrigo Richard; Silva, Nelson Renato França Alves; Moreira, Allysson Nogueira

    2016-06-01

    Threaded metal pins have been used to create additional retention for large composite resin restorations. However, their dark appearance may compromise esthetic outcome. The use of small fiberglass posts has been advocated as an alternative. This clinical report describes a mini fiberglass post (MFP) used to provide additional retention in a fractured anterior tooth that received a composite resin restoration. The MFP represents a promising option for creating additional retention for large composite resin restorations. PMID:26724848

  2. Synthesis and Thermal Degradation Studies of Melamine Formaldehyde Resins

    PubMed Central

    Ullah, Sami; Bustam, M. A.; Nadeem, M.; Tan, W. L.; Shariff, A. M.

    2014-01-01

    Melamine formaldehyde (MF) resins have been synthesized at different reaction temperature and pH values. Different molar ratios of melamine and formaldehyde were used to synthesize the corresponding resins. The prepared resin samples were characterized by using molecular weight determination viscometry and thermogravimetric analysis (TGA). The maximum percentage of solid content (69.7%) was obtained at pH 8.5 and 75°C temperature. The molecular weight of MF resin was increased with an increase of melamine monomer concentration. The highest residual weight 14.125 wt.% was obtained with sample 10. PMID:25436237

  3. High T(sub g) Polymides for Resin Transfer Molding

    NASA Technical Reports Server (NTRS)

    Chuang, Kathy C.; Criss, Jim M., Jr.; Mintz, Eric A.; Shonkwiler, Brian; Scheiman, Daniel A.; Nguyen, Baochau; McCorkle, Linda S.; Hardy-Green, DeNise

    2005-01-01

    A series of new polyimide resins with low melt viscosities and high glass transition temperatures (T(sub g)'s) of 340-350 C were developed for resin transfer molding (RTM) applications. The viscosities of these polyimide resins, based on 2,3,3'4'-Biphenyltetracarboxylic Dianhydride (a-BPDA), are in the range of 10-30 poise. The composites were fabricated successfully at 260-280 C with a pot life of 30-60 minutes by the RTM process. The viscosity profiles of the polyimide resins and the mechanical properties of the polyimide carbon fiber composites will be discussed.

  4. Acetylene-chromene terminated resins as high temperature thermosets

    NASA Technical Reports Server (NTRS)

    Godschalx, J. P.; Inbasekaran, M. N.; Bartos, B. R.; Scheck, D. M.; Laman, S. A.

    1990-01-01

    A novel phase transfer catalyzed process for the preparation of propargyl ethers has been developed. The propargyl ethers serve as precursors to a new class of thermosetting resins called acetylene-chromene terminated (ACT) resins. Heat treatment of a solution of propargyl ethers with various catalysts, followed by removal of solvent leads to the ACT resins via partial conversion of the propargyl ether groups to chromenes. This process reduces the energy content of the resin systems and reduces the amount of shrinkage found during cure. Due to the presence of the solvent the process is safe and gives rise to low viscosity products suitable for resin transfer molding and filament winding type applications. Due to the high glass transition temperature, high modulus, and low moisture uptake the cured resins display better than 232 C/wet performance. The thermal stability of the ACT resins in air at 204 C is superior to that of conventional bismaleimide resins. The resins also display excellent electrical properties.

  5. Branched polymeric media: boron-chelating resins from hyperbranched polyethylenimine.

    PubMed

    Mishra, Himanshu; Yu, Changjun; Chen, Dennis P; Goddard, William A; Dalleska, Nathan F; Hoffmann, Michael R; Diallo, Mamadou S

    2012-08-21

    Extraction of boron from aqueous solutions using selective resins is important in a variety of applications including desalination, ultrapure water production, and nuclear power generation. Today's commercial boron-selective resins are exclusively prepared by functionalization of styrene-divinylbenzene (STY-DVB) beads with N-methylglucamine to produce resins with boron-chelating groups. However, such boron-selective resins have a limited binding capacity with a maximum free base content of 0.7 eq/L, which corresponds to a sorption capacity of 1.16 ± 0.03 mMol/g in aqueous solutions with equilibrium boron concentration of ∼70 mM. In this article, we describe the synthesis and characterization of a new resin that can selectively extract boron from aqueous solutions. We show that branched polyethylenimine (PEI) beads obtained from an inverse suspension process can be reacted with glucono-1,5-D-lactone to afford a resin consisting of spherical beads with high density of boron-chelating groups. This resin has a sorption capacity of 1.93 ± 0.04 mMol/g in aqueous solution with equilibrium boron concentration of ∼70 mM, which is 66% percent larger than that of standard commercial STY-DVB resins. Our new boron-selective resin also shows excellent regeneration efficiency using a standard acid wash with a 1.0 M HCl solution followed by neutralization with a 0.1 M NaOH solution. PMID:22827255

  6. Properties of modified anhydride hardener and its cured resin

    NASA Astrophysics Data System (ADS)

    Qiang, Chen; Bingjun, Gao; Jinglin, Chen; Tongzhao, Xu

    2000-01-01

    Methyl-nadic-tetrahydric-methylanhydride (MNA), nadic-tetrahydric-methylanhydride (NA), anhydride hardener was modified by solid diol molecule to improve the impregnation resin fracture toughness in cryogenic temperature. The lap-shear strength, transverse tension as well as the thermal shock test showed that the resin cured by the modified anhydride hardener had higher bond strength and more toughness at 77 K. After the experiment of vacuum pressure impregnation (VPI) processing, it was found that this resin had a longer usable life, better impregnating properties, but higher initial viscosity than the resin hybrid HY925 as hardener.

  7. Acrylic resin injection method for blood vessel investigations.

    PubMed

    Suwa, Fumihiko; Uemura, Mamoru; Takemura, Akimichi; Toda, Isumi; Fang, Yi-Ru; Xu, Yuan Jin; Zhang, Zhi Yuan

    2013-01-01

    The injection of acrylic resin into vessels is an excellent method for macroscopically and microscopically observing their three-dimensional features. Conventional methods can be enhanced by removal of the polymerization inhibitor (hydroquinone) without requiring distillation, a consistent viscosity of polymerized resin, and a constant injection pressure and speed. As microvascular corrosion cast specimens are influenced by viscosity, pressure, and speed changes, injection into different specimens yields varying results. We devised a method to reduce those problems. Sodium hydroxide was used to remove hydroquinone from commercial methylmethacrylate. The solid polymer and the liquid monomer were mixed using a 1 : 9 ratio (low-viscosity acrylic resin, 9.07 ± 0.52 mPa•s) or a 3:7 ratio (high-viscosity resin, 1036.33 ± 144.02 mPa•s). To polymerize the acrylic resin for injection, a polymerization promoter (1.0% benzoyl peroxide) was mixed with a polymerization initiator (0.5%, N, N-dimethylaniline). The acrylic resins were injected using a precise syringe pump, with a 5-mL/min injection speed and 11.17 ± 1.60 mPa injection pressure (low-viscosity resin) and a 1-mL/min injection speed and 58.50 ± 5.75 mPa injection pressure (high-viscosity resin). Using the aforementioned conditions, scanning electron microscopy indicated that sufficient resin could be injected into the capillaries of the microvascular corrosion cast specimens. PMID:24107720

  8. Sorption of organics from aqueous solution onto polymeric resins

    SciTech Connect

    Gusler, G.M.; Browne, T.E.; Cohen, Y. . Dept. of Chemical Engineering)

    1993-11-01

    The uptake of phenol, toluene, chlorobenzene, and benzoic acid by several polymeric resins and activated carbon was investigated experimentally. Presentation of the sorption data in terms of the number of sorbed monolayers and fractional pore volume filled indicated that, for the polymeric resins, solute uptake cannot be viewed as only a surface adsorption phenomenon. It is suggested that the aqueous phase uptake of phenol, toluene, chlorobenzene, and benzoic acid by the polymeric resins is attributable, in part, to solute absorption. The present study also suggests that solute uptake is affected by the swelling of some of the polymeric resins in water.

  9. Ageing of resin from Pinus species assessed by infrared spectroscopy.

    PubMed

    Beltran, Victòria; Salvadó, Nati; Butí, Salvador; Pradell, Trinitat

    2016-06-01

    Resins obtained from Pinus genus species have been widely used in very different fields throughout history. As soon as the resins are secreted, molecular changes start altering their chemical, mechanical and optical properties. The ageing processes are complex, and the chemical and structural changes associated with resin degradation are not yet fully known. Many questions still remain open, for instance changes happening in pimaranes, one of the two diterpenoid constituents of the resin. A systematic study of the ageing process of Pinus resins is done through Fourier transform infrared spectroscopy (FTIR) using chemical standards and complementing the obtained results with gas chromatography coupled to mass spectrometry (GC/MS) analysis when necessary. Moreover, long-term degradation processes are also investigated through the analysis of a selection of dated historical resins. This study overcomes the limitations of GC/MS and brings new information about the reactions and interactions between molecules during Pinus resin ageing processes. It also provides information about which bonds are affected and unaffected, and these can be used as specific markers of the degradation and of the resins themselves. Graphical Abstract Changes in the IR spectral features due to the Pinus resin ageing processes. PMID:27052772

  10. 21 CFR 172.215 - Coumarone-indene resin.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... grapefruit, lemons, limes, oranges, tangelos, and tangerines in accordance with the following prescribed..., lemons, limes, oranges, tangelos, and tangerines whereby the maximum amount of the resin remaining on...

  11. Synthesis and thermal degradation studies of melamine formaldehyde resins.

    PubMed

    Ullah, Sami; Bustam, M A; Nadeem, M; Naz, M Y; Tan, W L; Shariff, A M

    2014-01-01

    Melamine formaldehyde (MF) resins have been synthesized at different reaction temperature and pH values. Different molar ratios of melamine and formaldehyde were used to synthesize the corresponding resins. The prepared resin samples were characterized by using molecular weight determination viscometry and thermogravimetric analysis (TGA). The maximum percentage of solid content (69.7%) was obtained at pH 8.5 and 75°C temperature. The molecular weight of MF resin was increased with an increase of melamine monomer concentration. The highest residual weight 14.125 wt.% was obtained with sample 10. PMID:25436237

  12. Report on use of XAD resins in racing chemistry.

    PubMed

    Johnston, G H

    1976-10-01

    This report comprises a summary of the work done with XAD resin extraction by racing chemists and reported in the Association of Official Racing Chemists publications. It is apparent that the use of XAD resins is becoming more popular in racing laboratories as a technique for routine screening and also for the extraction of certain conjugated drugs. Most laboratories employ variations on the original Brinkmann Drug-Skreen Technique. Comparisons of the efficiency of extraction of drugs from horse urine by XAD-2 resin and by chloroform column extraction indicate that some drugs can be extracted with equal or greater efficiency by the resin technique. PMID:1000159

  13. Analysis of residual stress in the resin of metal-resin adhesion structures by scanning acoustic microscopy.

    PubMed

    Ohno, Hiroki; Endo, Kazuhiko; Nagano-Takebe, Futami; Ida, Yusuke; Kakino, Ken; Narita, Toshio

    2013-01-01

    The residual stress caused by polymerization shrinkage and thermal contraction of a heat-curing resin containing 4-META on a metal-resin structure was measured by a scanning acoustic microscope. The tensile residual stress in the resin occurred within 70 µm of the adhesion interface with a flat plate specimen. The maximum tensile stress was about 58 MPa at the interface. On a metal plate specimen with retention holes, ring-like cracks in the resin occurred around the retention holes with the adhesive specimen and many linear cracks occurred in the resin vertical to the longitudinal direction of the metal frame with the non-adhesive specimens. There was tensile residual stress on the resin surface at the center of the retention holes of the adhesion specimen, indicating that the stress in the specimen with surface treatment for adhesion was higher than in that without surface treatment. PMID:24240901

  14. [Bond strength of etched enamel to direct composite resins, to indirect composite resins and to etched and silanized porcelain].

    PubMed

    Prévost, A P; Desautels, P

    1990-07-01

    The adhesion to enamel of composite resin inlays are not documented as much as porcelain inlays and direct composite resins. This study evaluates the adhesion of a light cured composite resin (P-50) used in an indirect technique and secondarily polymerized by heat. No significant differences were found between adhesion of P-50 used with an indirect technique and adhesion of porcelain (Mirage). P-50 used with the direct technique yield adhesion values significantly lower than the indirect techniques. PMID:2204471

  15. Improved epoxy resin for constructing cryogenic filament-wound pressure vessels

    NASA Technical Reports Server (NTRS)

    Molho, R.; Soffer, L. M.

    1971-01-01

    Mechanical properties of new resin at cryogenic temperatures are substantially improved over similar composite structures utilizing conventional resins, while properties at ambient temperature are identical to conventional resin composites.

  16. 21 CFR 178.3610 - α-Methylstyrene-vinyltoluene resins, hydrogenated.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... resins, hydrogenated. Hydrogenated α-methylstyrene-vinyltoluene copolymer resins having a molar ratio of...-vinyltoluene copolymer resins have a drop-softening point of 125° to 165 °C and a maximum absorptivity of...

  17. 21 CFR 178.3610 - α-Methylstyrene-vinyltoluene resins, hydrogenated.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... resins, hydrogenated. Hydrogenated α-methylstyrene-vinyltoluene copolymer resins having a molar ratio of...-vinyltoluene copolymer resins have a drop-softening point of 125° to 165 °C and a maximum absorptivity of...

  18. Characterization of Composite Fan Case Resins

    NASA Technical Reports Server (NTRS)

    Dvoracek, Charlene M.

    2004-01-01

    The majority of commercial turbine engines that power today s aircraft use a large fan driven by the engine core to generate thrust which dramatically increases the engine s efficiency. However, if one of these fan blades fails during flight, it becomes high energy shrapnel, potentially impacting the engine or puncturing the aircraft itself and thus risking the lives of passengers. To solve this problem, the fan case must be capable of containing a fan blade should it break off during flight. Currently, all commercial fan cases are made of either just a thick metal barrier or a thinner metal wall surrounded by Kevlar-an ultra strong fiber that elastically catches the blade. My summer 2004 project was to characterize the resins for a composite fan case that will be lighter and more efficient than the current metal. The composite fan case is created by braiding carbon fibers and injecting a polymer resin into the braid. The resin holds the fibers together, so at first using the strongest polymer appears to logically lead to the strongest fan case. Unfortunately, the stronger polymers are too viscous when melted. This makes the manufacturing process more difficult because the polymer does not flow as freely through the braid, and the final product is less dense. With all of this in mind, it is important to remember that the strength of the polymer is still imperative; the case must still contain blades with high impact energy. The research identified which polymer had the right balance of properties, including ease of fabrication, toughness, and ability to transfer the load to the carbon fibers. Resin deformation was studied to better understand the composite response during high speed impact. My role in this research was the testing of polymers using dynamic mechanical analysis and tensile, compression, and torsion testing. Dynamic mechanical analysis examines the response of materials under cyclic loading. Two techniques were used for dynamic mechanical analysis

  19. Reactive Additives for Phenylethynyl-Containing Resins

    NASA Technical Reports Server (NTRS)

    Connell, John W.; Smith, Joseph G., Jr.; Hergenrother, Paul M.; Rommel, Monica L.

    2005-01-01

    Phenylethynyl-containing reactive additive (PERA) compounds and mixtures have been found to be useful for improving the processability of oligomers, polymers, co-oligomers, and copolymers that contain phenylethynyl groups. The additives can be incorporated in different forms: A solution of an amide acid or an imide of a PERA can be added to a solution of phenylethynyl-containing oligomer, polymer, co-oligomer, or copolymer; or An imide powder of a PERA can be mixed with a dry powder of a phenylethynyl-containing oligomer, polymer, co-oligomer, or copolymer. The effect of a given PERA on the processability and other properties of the resin system depends on whether the PERA is used in the amide acid or an imide form. With proper formulation, the PERA reduces the melt viscosity of the resin and thereby reduces the processing pressures needed to form the adhesive bonds, consolidate filled or unfilled moldings, or fabricate fiber-reinforced composite laminates. During thermal cure, a PERA reacts with itself as well as with the phenylethynyl-containing host resin and thereby becomes chemically incorporated into the resin system. The effects of the PERA on mechanical properties, relative to those of the host resin, depend on the amount of PERA used. Typically, the incorporation of the PERA results in (1) increases in the glass-transition temperature (Tg), modulus of elasticity, and parameters that characterize behavior under compression, and (2) greater retention of the aforementioned mechanical properties at elevated temperatures without (3) significant reduction of toughness or damage tolerance. Of the formulations tested thus far, the ones found to yield the best overall results were those for which the host resin was the amide acid form of a phenylethynyl-terminated imide (PETI) co-oligomer having a molecular weight of 5,000 g/mole [hence, designated PETI-5] and a PERA denoted as PERA-1. PETI-5 was made from 3,3',4'4'-biphenyltetracarboxylic dianhydride, 3

  20. HIGH ASPECT RATIO ION EXCHANGE RESIN BED - HYDRAULIC RESULTS FOR SPERICAL RESIN BEADS

    SciTech Connect

    Duignan, M; Charles Nash, C; Timothy Punch, T

    2007-09-27

    A principal role of the DOE Savannah River Site is to safely dispose of a large volume of liquid nuclear waste held in many storage tanks. An in-tank ion exchange unit is being considered for cesium removal to accelerate waste processing. This unit is planned to have a relatively high bed height to diameter ratio (10:1). Complicating the design is the need to cool the ion exchange media; therefore, the ion exchange column will have a central cooling core making the flow path annular. To separate cesium from waste the media being considered is made of resorcinol formaldehyde resin deposited on spherical plastic beads and is a substitute for a previously tested resin made of crystalline silicotitanate. This spherical media not only has an advantage of being mechanically robust, but, unlike its predecessor, it is also reusable, that is, loaded cesium can be removed through elution and regeneration. Resin regeneration leads to more efficient operation and less spent resin waste, but its hydraulic performance in the planned ion exchange column was unknown. Moreover, the recycling process of this spherical resorcinol formaldehyde causes its volume to significantly shrink and swell. To determine the spherical media's hydraulic demand a linearly scaled column was designed and tested. The waste simulant used was prototypic of the wastes' viscosity and density. This paper discusses the hydraulic performance of the media that will be used to assist in the design of a full-scale unit.

  1. Evaluating resin-enamel bonds by microshear and microtensile bond strength tests: effects of composite resin

    PubMed Central

    de ANDRADE, Andrea Mello; MOURA, Sandra Kiss; REIS, Alessandra; LOGUERCIO, Alessandro Dourado; GARCIA, Eugenio Jose; GRANDE, Rosa Helena Miranda

    2010-01-01

    Objectives The aims of this study were to evaluate the effect of resin composite (Filtek Z250 and Filtek Flow Z350) and adhesive system [(Solobond Plus, Futurabond NR (VOCO) and Adper Single Bond (3M ESPE)] on the microtensile (µTBS) and microshear bond strength (µSBS) tests on enamel, and to correlate the bond strength means between them. Material and methods Thirty-six extracted human molars were sectioned to obtain two tooth halves: one for µTBS and the other one for µSBS. Adhesive systems and resin composites were applied to the enamel ground surfaces and light-cured. After storage (37ºC/24 h) specimens were stressed (0.5 mm/ min). Fracture modes were analyzed under scanning electron microscopy. The data were analyzed using two-way ANOVA and Tukey's test (α=0.05). Results The correlation between tests was estimated with Pearson's product-moment correlation statistics (α =0.05). For both tests only the main factor resin composite was statistically significant (p<0.05). The correlation test detected a positive (r=0.91) and significant (p=0.01) correlation between the tests. Conclusions The results were more influenced by the resin type than by the adhesives. Both microbond tests seem to be positive and linearly correlated and can therefore lead to similar conclusions. PMID:21308290

  2. Ion Exchange Temperature Testing with SRF Resin - 12088

    SciTech Connect

    Russell, R.L.; Rinehart, D.E.; Brown, G.N.; Peterson, R.A.

    2012-07-01

    Ion exchange using the Spherical Resorcinol-Formaldehyde (SRF) resin has been selected by the U.S. Department of Energy's Office of River Protection for use in the Pretreatment Facility of the Hanford Tank Waste Treatment and Immobilization Plant (WTP) and for potential application in an at-tank deployment for removing Cs-137. Recent proposed changes to the WTP ion exchange process baseline indicate that higher temperatures (50 deg. C) to alleviate post-filtration precipitation issues prior to reaching the ion exchange columns may be required. Therefore, it is important to understand the behavior of SRF resin performance under the conditions expected with the new equipment and process changes. This research examined the impact of elevated temperature on resin loading and resin degradation during extended solution flow at elevated temperature (45 deg., 50 deg., 55 deg., 60 deg., 65 deg., 75 deg. C). Testing for extended times at elevated temperatures showed that the resin does degrade and loading capacity is reduced at and above 45 deg. C. Above 60 deg. C the resin appears to not load at all. It was observed that the resin disintegrated at 75 deg. C until not much was left and partially disintegrated at 65 deg. C, which caused the column to plug in both tests after ∼336 hours. The results indicate that WTP will lose resin loading capacity if the ion exchange process is performed above 25 deg. C, and the resin will disintegrate above 65 deg. C. Therefore, WTP will have a restricted operating range of temperatures to perform the ion exchange process with this resin. PNNL and WTP are currently evaluating the operating limits of the resin in further detail. Aging in 0.5 M HNO{sub 3} also caused the resin to lose capacity above 25 deg. C and to completely dissolve at 55 deg. C. Again, WTP will have a restricted operating range of temperatures when eluting the resin with nitric acid in order to maintain resin loading capacity and avoid disintegration of the resin

  3. Microshear bond strength of composite resins to enamel and porcelain substrates utilizing unfilled versus filled resins

    PubMed Central

    Najafi-Abrandabadi, Ahmad; Najafi-Abrandabadi, Siamak; Ghasemi, Amir; Kotick, Philip G.

    2014-01-01

    Background: Failures such as marginal discoloration and composite chipping are still the problems of tooth-colored restorations on the substrate of enamel and porcelain, which some of these problems are consequently as a result of failures in the bonding layer. Using filled resin has been recently introduced to increase the bond strength of this layer. The aim of this study was to compare the microshear bond strength (μ-SBS) of composite resins to enamel incubated in periods of 24 h and 9 months and porcelain with unfilled resin and flowable composites (filled resin). Materials and Methods: In this in vitro study, two groups of 75 enamel samples with different storage times (24 h and 9 months) and a group of 75 porcelain samples were used. They were divided into 5 experimental groups of 15 samples in each. Composite cylinders in tygon tubes were bonded on the surface of acid-etched enamel and pretreated porcelain. Wave, Wave MV, Wave HV, Grandioflow and Margin Bond were used as bonding agents. The μ-SBS was measured at the speed of 1.0 mm/min. The bond strengths were analyzed with one-way analysis of variance (ANOVA) test followed by Tukey test. P < 0.05 was selected as the level of statistical significance in this study. Results: The results showed that for enamel (24 h), the μ-SBS of the Wave MV and Wave HV groups were significantly lower than the Margin Bond group. Tukey test indicated the absence of a significant difference between the μ-SBS of the Wave group and the Margin Bond group. However, the μ-SBS of the Grandioflow group was significantly higher than the one for the Margin Bond as a bonding agent. In enamel (9 months), there was a significant difference between the Grandioflow and Margin Bond groups. Regarding bonding to the porcelain the one-way ANOVA test did not show a significant difference among the groups. Conclusion: This study revealed that flowable composites (filled resins) can be used instead of unfilled resins in bonding composite

  4. Isothermal aging effects on PMR-15 resin

    NASA Technical Reports Server (NTRS)

    Bowles, Kenneth J.; Jayne, Douglas; Leonhardt, Todd A.

    1992-01-01

    Specimens of PMR-15 polyimide neat resin were aged in air at temperatures of 288, 316, and 343 C. Weight losses and dimensional changes were monitored during the course of the exposure time. Physical changes were also observed by optical and electron microscopy. It was found that polyimide polymer degradation occurred within a thin surface layer that developed and grew during thermal aging. The cores of the polymer specimens were protected from oxidative degradation, and they were relatively unchanged by the thermal treatment. Surface cracking was observed at 343 C and was probably due to an interaction between voids and stresses that developed in the surface layer.

  5. Organic ion exchange resin separation methods evaluation

    SciTech Connect

    Witwer, K.S.

    1998-05-27

    This document describes testing to find effective methods to separate Organic Ion Exchange Resin (OIER) from a sludge simulant. This task supports a comprehensive strategy for treatment and processing of K-Basin sludge. The simulant to be used resembles sludge that has accumulated in the 105KE and 105KW Basins in the 1OOK area of the Hanford Site. The sludge is an accumulation of fuel element corrosion products, organic and inorganic ion exchange materials, canister gasket materials, iron and aluminum corrosion products, sand, dirt, and other minor amounts of organic matter.

  6. Electroactive polymer gels based on epoxy resin

    NASA Astrophysics Data System (ADS)

    Samui, A. B.; Jayakumar, S.; Jayalakshmi, C. G.; Pandey, K.; Sivaraman, P.

    2007-04-01

    Five types of epoxy gels have been synthesized from common epoxy resins and hardeners. Fumed silica and nanoclay, respectively, were used as fillers and butyl methacrylate/acrylamide were used as monomer(s) for making interpenetrating polymer networks (IPNs) in three compositions. Swelling study, tensile property evaluation, dynamic mechanical thermal analysis, thermo-gravimetric analysis, scanning electron microscopy and electroactive property evaluation were done. The gels have sufficient mechanical strength and the time taken for bending to 20° was found to be 22 min for forward bias whereas it was just 12 min for reverse bias.

  7. Resin catalysts and method of preparation

    DOEpatents

    Smith, Jr., Lawrence A.

    1986-01-01

    Heat stabilized catalyst compositions are prepared from nuclear sulfonic acid, for example, macroporous crosslinked polyvinyl aromatic compounds containing sulfonic acid groups are neutralized with a metal of Al, Fe, Zn, Cu, Ni, ions or mixtures and alkali, alkaline earth metals or ammonium ions by contacting the resin containing the sulfonic acid with aqueous solutions of the metals salts and alkali, alkaline earth metal or ammonium salts. The catalysts have at least 50% of the sulfonic acid groups neutralized with metal ions and the balance of the sulfonic acid groups neutralized with alkali, alkaline earth ions or ammonium ions.

  8. Resin catalysts and method of preparation

    DOEpatents

    Smith, L.A. Jr.

    1986-12-16

    Heat stabilized catalyst compositions are prepared from nuclear sulfonic acid, for example, macroporous crosslinked polyvinyl aromatic compounds containing sulfonic acid groups are neutralized with a metal of Al, Fe, Zn, Cu, Ni, ions or mixtures and alkali, alkaline earth metals or ammonium ions by contacting the resin containing the sulfonic acid with aqueous solutions of the metals salts and alkali, alkaline earth metal or ammonium salts. The catalysts have at least 50% of the sulfonic acid groups neutralized with metal ions and the balance of the sulfonic acid groups neutralized with alkali, alkaline earth ions or ammonium ions.

  9. Organic geochemistry of resins from modern Agathis australis and Eocene resins from New Zealand: Diagenetic and taxonomic implications

    USGS Publications Warehouse

    Lyons, P.C.; Mastalerz, Maria; Orem, W.H.

    2009-01-01

    A maturation series of resins and fossil resins from New Zealand, ranging in age from Modern to Eocene and ranging from uncoalified to high volatile C bituminous coal, were analyzed by elemental, pyrolysis-gas chromatography (Py-GC), Fourier Transform infrared (FTir), and solid-state 13C nuclear magnetic resonance (13C NMR) techniques. For comparison, four resin samples from the Latrobe Valley, Australia, were analyzed. All of the resins and fossil resins of this study show very high H/C atomic ratios, and are characterized by dominant peaks in the 10-60??ppm range of solid-state 13C NMR spectra and prominent bands in the aliphatic stretching region (2800-3000??cm- 1) of FTir spectra, all indicating a highly aliphatic molecular structure. The 13C NMR and FTir data indicate a diterpenoid structure for these resins. There is an abrupt loss of oxygen that occurs at the Lignite A/Subbituminous C stage, which is attributed to a dramatic loss of carboxyl (COOH) from the diterpenoid molecule. This is a new finding in the diagenesis of resins. This important loss in oxygenated functional groups is attributed to a maturation change. Also, there is a progressive loss of exomethylene (CH2) groups with increasing degree of maturation, as shown by both 13C NMR and FTir data. This change has been noted by previous investigators. Exomethylene is absent in the fossil resins from the Eocene high volatile C bituminous coals. This progressive loss is characteristic of Class I resinites. FTir data indicate that the oxygenated functional groups are strong in all the resin samples except the fossil resin from high volatile C bituminous coal. This important change in oxygenated functional groups is attributed to maturation changes. The 13C NMR and FTir data indicate there are minor changes in the Agathis australis resin from the living tree and soil, which suggests that alteration of A. australis resins begins shortly after deposition in the soil for as little as 1000??years. The Morwell

  10. A Comparison of Shear Bond Strength of Ceramic and Resin Denture Teeth on Different Acrylic Resin Bases

    PubMed Central

    Corsalini, Massimo; Venere, Daniela Di; Pettini, Francesco; Stefanachi, Gianluca; Catapano, Santo; Boccaccio, Antonio; Lamberti, Luciano; Pappalettere, Carmine; Carossa, Stefano

    2014-01-01

    The purpose of this study is to compare the shear bond strength of different resin bases and artificial teeth made of ceramic or acrylic resin materials and whether tooth-base interface may be treated with aluminium oxide sandblasting. Experimental measurements were carried on 80 specimens consisting of a cylinder of acrylic resin into which a single tooth is inserted. An ad hoc metallic frame was realized to measure the shear bond strength at the tooth-base interface. A complete factorial plan was designed and a three-way ANalysis Of VAriance (ANOVA) was carried out to investigate if shear bond strength is affected by the following factors: (i) tooth material (ceramic or resin); (ii) base material (self-curing or thermal-curing resin); (iii) presence or absence of aluminium oxide sandblasting treatment at the tooth-base interface. Tukey post hoc test was also conducted to evaluate any statistically significant difference between shear strength values measured for the dif-ferently prepared samples. It was found from ANOVA that the above mentioned factors all affect shear strength. Furthermore, post hoc analysis indi-cated that there are statistically significant differences (p-value=0.000) between measured shear strength values for: (i) teeth made of ceramic material vs. teeth made of acrylic resin material; (ii) bases made of self-curing resin vs. thermal-curing resin; (iii) specimens treated with aluminium oxide sandblasting vs. untreated specimens. Shear strength values measured for acryl-ic resin teeth were on average 70% higher than those measured for ceramic teeth. The shear bond strength was maximized by preparing samples with thermal-curing resin bases and resin teeth submitted to aluminium oxide sandblasting. PMID:25614770

  11. 76 FR 8774 - Granular Polytetrafluoroethylene Resin From Japan

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-02-15

    ... December 22, 2010, because ``the domestic parties did not participate in this review.'' (76 FR 3614... COMMISSION Granular Polytetrafluoroethylene Resin From Japan AGENCY: United States International Trade... polytetrafluoroethylene resin from Japan would be likely to lead to continuation or recurrence of material injury....

  12. 75 FR 67105 - Granular Polytetrafluoroethylene Resin From Italy and Japan

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-11-01

    ... granular polytetrafluoroethylene resin from Japan (53 FR 32267). On August 30, 1988, Commerce issued an... from Italy and Japan (65 FR 6147, February 8, 2000). Following second five-year reviews by Commerce and... orders on imports of granular polytetrafluoroethylene resin from Italy and Japan (70 FR 76026)....

  13. Sand control in wells with gas generator and resin

    SciTech Connect

    Dees, J.M.

    1992-04-07

    This patent describes a method of treating a wellbore having formation perforations for controlling sand and other fine materials. It comprises positioning a quantity of fluid resin material in alignment with the formation perforations of the wellbore; positioning a gas generator in proximity with the fluid resin material; actuating the gas generator to increase wellbore pressure in a substantially instantaneous manner to a pressure substantially in excess of well pressure to force the fluid resin material from the wellbore into the formation perforations; and subsequently polymerizing the resin material to form a consolidated, porous, permeable matrix which retains the sand and other fine materials while permitting the flow of production fluid into the wellbore. This paper also describes a method of treating a wellbore having formation perforations for controlling sand and other fine materials. It comprises positioning a coiled tubing, having a valve and gas generator attached thereto, so that the valve is positioned in a predetermined location relative to the bottom formation perforation; injecting a predetermined amount of fluid resin material through the coiled tubing and valve into the wellbore; raising the gas generator to a position across the formation perforations and in proximity with the fluid resin material; actuating the gas generator to force the fluid resin material into the formation perforations; and thereafter polymerizing the previously fluid resin material to form a consolidated, porous, permeable matrix which retains the sand and other fine materials while permitting the flow of production fluid into the wellbore.

  14. 21 CFR 173.10 - Modified polyacrylamide resin.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... CONSUMPTION Polymer Substances and Polymer Adjuvants for Food Treatment § 173.10 Modified polyacrylamide resin... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Modified polyacrylamide resin. 173.10 Section 173.10 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES...

  15. 21 CFR 173.10 - Modified polyacrylamide resin.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... CONSUMPTION Polymer Substances and Polymer Adjuvants for Food Treatment § 173.10 Modified polyacrylamide resin... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Modified polyacrylamide resin. 173.10 Section 173.10 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES...

  16. 21 CFR 872.3200 - Resin tooth bonding agent.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Resin tooth bonding agent. 872.3200 Section 872.3200 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3200 Resin tooth bonding agent. (a)...

  17. Guayule resin detection and influence on guayule rubber

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Guayule (Parthenium argentatum) is a natural rubber (cis-1,4-polyisoprene) producing crop, native to North America. Guayule also produces organic resins, complex mixtures of terpenes, triglycerides, guayulins, triterpenoids and other components. During natural rubber extraction, guayule resins can b...

  18. 21 CFR 181.32 - Acrylonitrile copolymers and resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Acrylonitrile copolymers and resins. 181.32 Section 181.32 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) PRIOR-SANCTIONED FOOD INGREDIENTS Specific Prior-Sanctioned Food Ingredients § 181.32 Acrylonitrile copolymers and resins. (a)...

  19. SECURING CONTAINERIZED HAZARDOUS WASTES WITH POLYETHYLENE RESIN AND FIBERGLASS ENCAPSULATES

    EPA Science Inventory

    This study investigates the fabrication and use of polyethylene resin and fiberglass to encapsulate and secure containerized hazardous wastes. Laboratory-scale encapsulates of composite structure were made from powdered, high-density polyethylene (HDPE) and epoxy-resin-wetted fib...

  20. 21 CFR 173.40 - Molecular sieve resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... give a stable three dimensional structure. The resins have a pore size of 2.0 to 3.0 milliliters per gram of dry resin (expressed in terms of water regain), and a particle size of 10 to 300 microns....

  1. 21 CFR 173.40 - Molecular sieve resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... gram of dry resin (expressed in terms of water regain), and a particle size of 10 to 300 microns. (b) The molecular sieve resins are thoroughly washed with potable water prior to their first use in... purification of partially delactosed whey. The gel bed shall be maintained in a sanitary manner in...

  2. The measurement of polymerization shrinkage of composite resins with ESPI

    NASA Astrophysics Data System (ADS)

    Zhang, Zhang; Yang, Guo Biao

    2008-09-01

    In the current study, we used the method of electronic speckle pattern interferometry (ESPI) to measure polymerization shrinkage of composite resins. Standardized cavities were prepared and placed into the ESPI apparatus before the cavities were filled with composites (n=2) .The ESPI apparatus was constructed to measure the out-of-plane displacement of the resins surface during the polymerization. Experiments demonstrated that the ESPI technique was a viable method to measure the deformation of composite resins. It was responsive and sensitive to dimensional changes. We found that cavity shape, size and C- factor influenced the date of resins shrinkage. And the tooth deformation in response to polymerization of resins was measured by the ESPI too. We concluded that ESPI was a feasible method for assessing resins deformation induced by its polymerization shrinkage when it was bonded in tooth cavities. And the results were greatly influenced by the dimensions of cavities , or interface adhesive and so on. It could also measure the tooth deformation induced by shrinkage of bonded composite resins. We found that resins polymerization shrinkage date may overestimate shrinkage-induced tooth deformation.

  3. Evaluation of Elution Parameters for Cesium Ion Exchange Resins

    SciTech Connect

    Burgeson, Ingrid E.; Deschane, Jaquetta R.; Cook, Bryan J.; Blanchard, David L.; Weier, Dennis R.

    2006-08-28

    Cesium ion exchange is one of the planned processes for treating and disposing of waste at the U.S. Department of Energy Hanford Site. Radioactive supernatant liquids from the waste tanks will undergo ultrafiltration, followed by cesium ion exchange using a regenerable organic ion exchange resin. Two resins, SuperLig?644 and a Resorcinol-formaldehyde resin are being evaluated for cesium removal and cesium elution characteristics. The main purpose of this study is to optimize the cesium elution to provide a resin which after undergoing elution would meet the U.S. Department of Energy/Office of River Protection Project-Waste Treatment Plant processing and resin disposal criteria. Columns of each resin type were loaded to greater or equal to 90% breakthrough with a Hanford waste stimulant and eluted with nitric acid. The temperature, flow rate and nitric acid concentration were varied to determine the optimal elution conditions. Temperature and eluant flow rate were the most important elution parameters. As would be predicted based upon kinetic consideration alone, decreasing the eluant flow rate and increasing the temperature provided the optimal elution conditions. Varying the nitric acid concentration did not have a significant effect on the elution; however, elutions performed using both high acid concentration (1M) and elevated temperature (45 C) resulted in resin degradation, causing gas generation and resin bed disruption.

  4. Resin collection and social immunity in honey bees

    Technology Transfer Automated Retrieval System (TEKTRAN)

    We determined if the use of resins, complex plant secretions with diverse antimicrobial properties, acts as a colony-level immune defense by honey bees. Colonies were enriched with extracts of Brazilian or Minnesotan propolis (a bee mixture of resins and wax) or were left as controls. We measured ge...

  5. 21 CFR 177.1650 - Polysulfide polymer-polyepoxy resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1650 Polysulfide polymer-polyepoxy resins. Polysulfide polymer... polyfunctional epoxide resins, cured with the aid of tri(dimethylaminomethyl) phenol, to which have been...

  6. Characterization of DGEBA (diglycidyl ethers bisphenol-A) epoxy resins

    SciTech Connect

    Larsen, F.N.; Spieker, D.A.

    1987-04-01

    High-resolution gel permeation chromatography and high-performance liquid chromatography can be applied to commercially available DGEBA epoxy resins to elucidate small but significant differences in the oligomer and impurity compositions of these resins. The GPC profiles can be used to type or identify the various commercial grades of these DGEBA resins. Lot-to-lot consistency and aging characteristics can also be determined using GPC and HPLC. Quantitation of the various oligomers and impurities such as the ..cap alpha..-glycol, isomer, and chlorohydrin species is possible. Using 20% isoconversion predictive cure thermal analysis data, the relative resin reactivity of several liquid, low-molecular DGEBA resins has been measured. These data show that the higher viscosity, higher oligomer content resins, which have higher hydroxyl content, reacted faster with amine cure agents than the lower viscosity, higher purity - and consequently lower hydroxyl content - resins. Thus, a combination of liquid chromatography (GPC or HPLC) and DSC kinetics can be used to establish a correlation or equivalency beween the commercially available low-molecular-weight DGEBA epoxy resins.

  7. 21 CFR 872.3670 - Resin impression tray material.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 8 2012-04-01 2012-04-01 false Resin impression tray material. 872.3670 Section 872.3670 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3670 Resin impression tray material....

  8. 21 CFR 872.3670 - Resin impression tray material.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 8 2014-04-01 2014-04-01 false Resin impression tray material. 872.3670 Section 872.3670 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3670 Resin impression tray material....

  9. 21 CFR 872.3670 - Resin impression tray material.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 8 2011-04-01 2011-04-01 false Resin impression tray material. 872.3670 Section 872.3670 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3670 Resin impression tray material....

  10. 21 CFR 872.3670 - Resin impression tray material.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 8 2013-04-01 2013-04-01 false Resin impression tray material. 872.3670 Section 872.3670 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3670 Resin impression tray material....

  11. 21 CFR 177.2410 - Phenolic resins in molded articles.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Phenolic resins in molded articles. 177.2410... as Components of Articles Intended for Repeated Use § 177.2410 Phenolic resins in molded articles... articles intended for repeated use in contact with nonacid food (pH above 5.0), in accordance with...

  12. Method and solvent composition for regenerating an ion exchange resin

    DOEpatents

    Even, William R.; Irvin, David J.; Irvin, Jennifer A.; Tarver, Edward E.; Brown, Gilbert M.; Wang, James C. F.

    2002-01-01

    A method and composition for removing perchlorate from a highly selective ion exchange resin is disclosed. The disclosed approach comprises treating the resin in a solution of super critical or liquid carbon dioxide and one or more quaternary ammonium chloride surfactant compounds.

  13. Stochastic Flow Modeling for Resin Transfer Moulding

    NASA Astrophysics Data System (ADS)

    Desplentere, Frederik; Verpoest, Ignaas; Lomov, Stepan

    2009-07-01

    Liquid moulding processes suffer from inherently present scatter in the textile reinforcement properties. This variability can lead to unwanted filling patterns within the mould resulting in bad parts. If thermoplastic resins are used with the in-situ polymerisation technique, an additional difficulty appears. The time window to inject the material is small if industrial processing parameters are used (<5 minutes). To model the stochastic nature of RTM, Darcy's description of the mould filling process has been used with the permeability distribution of the preform given as a random field. The random field of the permeability is constructed as a correlated field with an exponential correlation function. Optical microscopy and X-ray micro-CT have been used to study the stochastic parameters of the geometry for 2D and 3D woven textile preforms. The parameters describing the random permeability field (average, standard deviation and correlation length) are identified based on the stochastic parameters of the geometry for the preforms, analytical estimations and CFD modelling of the permeability. In order to implement the random field for the permeability and the variability for the resin viscosity, an add-on to the mould filling simulation software PAM-RTM™ has been developed. This analysis has been validated on case studies.

  14. Radionuclide Leaching from Organic Ion Exchange Resin

    SciTech Connect

    Delegard, C.H.; Rinehart, D.E.

    1999-04-02

    Laboratory tests were performed to examine the efficacy of leach treatments for decontaminating organic ion exchange resins (OIER), which have been found in a number of samples retrieved from K East Basin sludge. Based on process records, the OIER found in the K Basins is a mixed-bet strong acid/strong base material marketed as Purolite{trademark} NRW-037. Radionuclides sorbed or associated with the OIER can restrict its disposal to the Environmental Restoration Disposal Facility (ERDF). The need for testing to support development of a treatment process for K Basin sludge has been described in Section 4.2 of ''Testing Strategy to Support the Development of K Basins Sludge Treatment Process'' (Flament 1998). To help understand the effects of anticipated OIER elutriation and washing, tests were performed with well-rinsed OIER material from K East Basin floor sludge (sample H-08 BEAD G) and with well-rinsed OIER having approximately 5% added K East canister composite sludge (sample KECOMP). The rinsed resin-bearing material also contained the inorganic ion exchanger Zeolon-900{trademark}, a zeolite primarily composed of the mineral mordenite. The zeolite was estimated to comprise 27 weight percent of the dry H-08 BEAD G material.

  15. Fluoride and chlorhexidine release from filled resins.

    PubMed

    Shen, C; Zhang, N-Z; Anusavice, K J

    2010-09-01

    Resin-based materials that release either fluoride or chlorhexidine have been formulated for inhibiting caries activity. It is not known if the two agents, when incorporated into one material, would interact and affect their release potential. We hypothesized that the ratio of fluoride to chlorhexidine incorporated into a resin, and the pH of the storage medium, will affect their releases from the material. The material investigated contained 23 wt% of filler, and the ratios of calcium fluoride to chlorhexidine diacetate were 8/2, 5/5, and 2/8. The release was conducted in pH 4, 5, and 6 acetate buffers. The results showed that release of either agent increased as the pH of the medium decreased. The presence of fluoride salt substantially reduced the chlorhexidine release, while the presence of a specific quantity of chlorhexidine significantly increased fluoride release. This interaction can be utilized to optimize the release of either agent for therapeutic purposes. PMID:20581354

  16. Resin Glycosides from the Morning Glory Family

    NASA Astrophysics Data System (ADS)

    Pereda-Miranda, Rogelio; Rosas-Ramírez, Daniel; Castañeda-Gómez, Jhon

    Resin glycosides are part of a very extensive family of secondary metabolites known as glycolipids or lipo-oligosaccharides and are constituents of complex resins (glycoresins) (1) unique to the morning glory family, Convolvulaceae (2). These active principles are responsible for the drastic purgative action of all the important Convolvulaceous species used in traditional medicine throughout the world since ancient times. Several commercial purgative crude drugs can be prepared from the roots of different species of Mexican morning glories. Their incorporation as therapeutic agents in Europe is an outstanding example of the assimilation of botanical drugs from the Americas as substitutes for traditional Old World remedies (3). Even though phytochemical investigations on the constituents of these drugs were initiated during the second half of the nineteenth century, the structure of their active ingredients still remains poorly known for some examples of these purgative roots. During the last two decades, the higher resolution capabilities of modern analytical isolation techniques used in conjunction with powerful spectroscopic methods have facilitated the elucidation of the active principles of these relevant herbal products.

  17. Perfluorotriethylene glycol dimethacrylate modified composite resins for improved dental restoratives

    NASA Astrophysics Data System (ADS)

    Wang, Guigui

    The studies described in this dissertation focus on improvement of water resistance and durability of current dental composite resins. The physical, thermal and mechanical properties of the diluent fluorinated monomer, perfluorotriethylene glycol methacrylate (FTEGDMA), FTEGDMA-containing neat resin and its formulated composite resins were evaluated and compared with the conventional visible light-cured (VLC) dental composite resins. Further, the biocompatibility of this monomer and its cured resins were investigated and compared with their conventional counterparts. The results showed that the FTEGDMA-containing neat resin and its composite systems showed more water resistance and longer durability, compared to the conventional Bisphenol A glycol dimethacrylate/triethylene glycol dimethacrylate (BisGMA/TEGDMA) system. The preliminary in vitro biocompatibility test showed that FTEGDMA favored cell growth, compared to the conventional dental resins. The first study investigated basic physical properties of the diluent FTEGDMA monomer. The results showed that the FTEGDMA exhibited lower viscosity, lower refractive index, and a smaller contact angle, which were all beneficial to lowering the water sorption and increasing hydrophobicity. The second study evaluated some physical, thermal, and mechanical properties of the FTEGDMA based neat resins, including polymerization shrinkage, contact angle, water sorption, glass-transitions, dynamic modulus, thermal expansion, compressive strength, and diametral tensile strength. The results showed that the FTEGDMA diluent exhibited significant less water sorption and lower polymerization shrinkage and the BisEMA also contributed towards reducing water sorption. The third study investigated the effects of the FTEGDMA on the mechanical properties of the composite resins including flexural strength (FS), diametral tensile strength (DTS) and wear resistance (WR). In addition, the fracture surface topography of the tested materials

  18. The sorption capacity of boron on anionic-exchange resin

    SciTech Connect

    Lou, J.; Foutch, G.L.; Na, J.W.

    1999-11-01

    Boron sorption capacities on anionic-exchange resins vary with temperature, concentration, and resin crosslinkage. A semiempirical correlation, developed from boron solution chemistry, is presented to account for these variations. The relationship, based on boron chemistry and changes in Gibb's energy, can be stated approximately as Q = a{sub 1}C{sub B}{sup a{sub 2}}Z{sup a{sub 3}} exp[{minus}(a{sub 4}T + a{sub 5}T{sup 2} + a{sub 6}Z{sup 0.5})]. Correlation parameters, which vary with resin type, are evaluated experimentally. Parameter values for macroporous resin Diaion PA 300 and for gel-type resins Diaion SA10 and Amberlite IRN 78LC are presented. The resulting expression is used to determine boron sorption and desorption limitations on ion exchangers at various temperatures and concentrations, and to determine the interfacial boron concentration in equilibrium and rate models.

  19. Microwave heated resin injector for advanced composite production.

    PubMed

    Stanculovic, Sebastijan; Feher, Lambert

    2008-01-01

    A novel microwave (MW) injector at 2.45 GHz for resin infiltration has been developed at the Institute for Pulsed Power and Microwave Technology (IHM), Research Center Karlsruhe (FZK), Germany. Resin injection is an essential step in the production of carbon fibre reinforced plastics (CFRP) for aerospace applications. A compact, low-cost and automated MW injector provides an efficient and safe energy transfer from the MW source to the resin and supports an appropriate electromagnetic field structure for homogeneous infiltration. The system provides temperature monitoring and an automatized MW power switching, which ensures a fast response of the MW system to rapid changes in the temperature for high flow rates of the resin. In low power measurements with a vector network analyzer, the geometry of the injector cavity has been adjusted to provide an efficient system. The MW injector has been tested for specific resin systems infiltrations. PMID:19227063

  20. Kinetic and thermodynamic studies of sulforaphane adsorption on macroporous resin.

    PubMed

    Yuanfeng, Wu; Lei, Zhang; Jianwei, Mao; Shiwang, Liu; Jun, Huang; Yuru, You; Lehe, Mei

    2016-08-15

    The adsorption equilibrium, kinetic and thermodynamic of sulforaphane (SF) adsorption onto macroporous resin in aqueous phase were studied. The SP850 resin was screened as the appropriate resin for SF purification. From the equilibrium studies, the Redlich-Peterson model was found to be the best for description of the adsorption behavior of SF onto SP850 resin, followed by the Freundlich model and the Langmuir model. Batch equilibrium experiments demonstrated that, in the examined temperature range, the equilibrium adsorption capacity of SP850 resin decreased with increasing adsorption temperature. Thermodynamics studies indicated that the adsorption of SF was a physical, exothermic, and spontaneous process. The adsorption kinetics revealed that the pseudo-second-order kinetic model was suitable to characterize the kinetics of adsorption of SF onto SP850. Finally, the intra-particle diffusion model demonstrated that SF diffused quickly into macropores, and that diffusion slowed down in the meso- and micropores. PMID:27391585

  1. Radiation degradation in EPICOR-2 ion exchange resins

    SciTech Connect

    McConnell, J.W. Jr.; Johnson, D.A.; Sanders, R.D. Sr.

    1990-09-01

    The Low-Level Waste Data base Development -- EPICOR-II Resin/Liner Investigation Program funded by the US Nuclear Regulatory Commission is investigating chemical and physical conditions for organic ion exchange resins contained in several EPICOR-II prefilters. Those prefilters were used during cleanup of contaminated water from the Three Mile Island Nuclear Power Station after the March 1979 accident. The work was performed by EG G Idaho, Inc. at the Idaho Engineering Laboratory. This is the final report of this task and summarizes results and analyses of three samplings of ion exchange resins from prefilters PF-8 and -20. Results are compared with baseline data from tests performed on unirradiated resins supplied by Epicor, Inc. to determine the extent of degradation due to the high internal radiation dose received by the organic resins. Results also are compared with those of other researchers. 18 refs., 23 figs., 7 tabs.

  2. Reliability of mechanical properties for bulk superconductors with resin impregnation

    NASA Astrophysics Data System (ADS)

    Tomita, M.; Murakami, M.; Katagiri, K.

    2002-10-01

    We have studied the mechanical properties of Y-Ba-Cu-O rods with and without resin impregnation using a three-point bending test. The reliability of resin impregnation was evaluated using the Weibull distribution function. The Weibull coefficient for the resin-impregnated bulk was 16.03 at 77 K. In order to obtain more reliable data, the bending strengths were converted into the tensile strengths by considering a difference in the effective volume. It was confirmed that the tensile strengths of bulk YBCO could be enhanced by more than four times with resin impregnation. It was also confirmed that resin-impregnated Y-Ba-Cu-O exhibited a high Weibull coefficient and thus a high reliability for practical engineering applications.

  3. Antimicrobial Assessment of Resins from Calophyllum Antillanum and Calophyllum Inophyllum.

    PubMed

    Cuesta-Rubio, Osmany; Oubada, Ahmad; Bello, Adonis; Maes, Louis; Cos, Paul; Monzote, Lianet

    2015-12-01

    The Calophyllum genus is well-known for its antimicrobial and cytotoxic activities, and therefore, we analyzed these biological activities for resins of Calophyllum antillanum and Calophyllum inophyllum growing in Cuba. C. antillanum resins showed a potent activity against Plasmodium falciparum (IC50  = 0.3 ± 0.1 µg/mL), while its cytotoxicity against MRC-5 cells was much lower (IC50  = 21.6 ± 1.1 µg/mL). In contrary, the resin of C. inophyllum showed an unspecific activity. The presence of apetalic acid, isoapetalic acid, calolongic acid, pinetoric acid I, pinetoric acid II, isocalolongic acid, pinetoric acid III, and isopinetoric acid III in C. antillanum resins was also confirmed. These results demonstrated for the first time the potential activity of C. antillanum resins against P. falciparum. PMID:26514875

  4. Chemical signatures of fossilized resins and recent plant exudates.

    PubMed

    Lambert, Joseph B; Santiago-Blay, Jorge A; Anderson, Ken B

    2008-01-01

    Amber is one of the few gemstones based on an organic structure. Found over most of the world, it is the fossil form of sticky plant exudates called resins. Investigation of amber by modern analytical techniques provides structural information and insight into the identity of the ancient plants that produced the source resin. Mass spectrometric analysis of materials separated by gas chromatography has identified specific compounds that are the basis of a reliable classification of the different types of amber. NMR spectroscopy of bulk, solid amber provides a complementary classification. NMR spectroscopy also can be used to characterize modern resins as well as other types of plant exudates such as gums, gum resins, and kinos, which strongly resemble resins in appearance but have very different molecular constitutions. PMID:18925589

  5. Removal of perfluorooctane sulfonate from wastewater by anion exchange resins: effects of resin properties and solution chemistry.

    PubMed

    Deng, Shubo; Yu, Qiang; Huang, Jun; Yu, Gang

    2010-10-01

    Perfluorooctane sulfonate (PFOS) is a new persistent organic pollutant of substantial environmental concern, and its removal from industrial wastewater is critical to eliminate its release into water environment. In this paper, six anion exchange resins with different polymer matrix, porosity, and functional group were evaluated for PFOS removal from simulated wastewater. Resin matrix displayed significant effect on the sorption kinetics and capacity of PFOS, and the polyacrylic resins including IRA67 and IRA958 exhibited faster sorption and higher sorption capacity for PFOS than the polystyrene resins due to the hydrophilic matrix. Sorption isotherms illustrated that the sorption capacity of PFOS on IRA67 and IRA958 was up to 4-5 mmol/g, and the amount of PFOS sorbed on the resins was more than chloride released from resins, indicating that other interactions besides anion exchange were involved in the sorption. Solution pH had little impact on the sorption of PFOS on IRA958, but displayed significant effect on IRA67 at pH above 10 due to the deprotonation of amine groups. The coexisting sulfate and hexavalent chromium in wastewater interfered with the sorption of PFOS because of their competitive sorption on the exchange sites. The spent resins were successfully regenerated using the mixture of NaCl and methanol solution. This work provided an understanding of sorption behavior and mechanism of PFOS on different anion exchange resins, and should result in more effective applications of ion exchange for PFOS removal from industrial wastewater. PMID:20605036

  6. 21 CFR 175.380 - Xylene-formaldehyde resins condensed with 4,4′-isopropylidenediphenol-epichlorohydrin epoxy resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Xylene-formaldehyde resins condensed with 4,4â²-isopropylidenediphenol-epichlorohydrin epoxy resins. 175.380 Section 175.380 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: ADHESIVES...

  7. 21 CFR 175.380 - Xylene-formaldehyde resins condensed with 4,4′-isopropylidenediphenol-epichlorohydrin epoxy resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Xylene-formaldehyde resins condensed with 4,4â²-isopropylidenediphenol-epichlorohydrin epoxy resins. 175.380 Section 175.380 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: ADHESIVES...

  8. Relined fiberglass post: an ex vivo study of the resin cement thickness and dentin-resin interface.

    PubMed

    Souza, Niélli Caetano de; Marcondes, Maurem Leitão; Breda, Ricardo Vaz; Weber, João Batista Blessmann; Mota, Eduardo Gonçalves; Spohr, Ana Maria

    2016-01-01

    The aim of this study was to evaluate the thickness of resin cements in the root thirds when using conventional fiberglass posts (CP) and relined fiberglass posts (RP) in weakened roots and to evaluate the morphological characteristics of the dentin-resin interface. Forty human maxillary anterior teeth had the crown sectioned below the cemento-enamel junction. The canals were endodontically treated and weakened with diamond burs. Teeth were divided into four groups (n = 10): Group 1 - CP + RelyX ARC; Group 2 - CP + RelyX U200; Group 3 - RP + RelyX ARC; and Group 4 - RP + RelyX U200. Prior to luting, 0.1% Fluorescein and 0.1% Rhodamine B dyes were added to an adhesive and resin cement, respectively. Slices were obtained from the apical, middle, and cervical thirds of the root. Confocal laser scanning microscopy images were recorded in four areas (buccal, lingual, mesial, distal) of each third. In each area, four equidistant measures of the resin cement were made and the mean value was calculated. The interface morphology was observed. The data were submitted to three-way ANOVA and Tukey's test (α = 0.05). The interaction between fiberglass posts, resin cement, and root thirds was significant (p < 0.0001). The resin cement thicknesses were significantly lower for RP in comparison with CP, except in the apical third. There was no significant difference between the resin cements for RP. There was formation of resin cement tags and adhesive tags along the root for RP. RP favored the formation of thin and uniform resin cement films and resin tags in weakened roots. PMID:27556553

  9. Microtensile bond strength of resin-resin interfaces after 24-hour and 2-month soaking.

    PubMed

    Leavitt, Curry; Boberick, Kenneth G; Winkler, Sheldon

    2007-01-01

    Evaluate the bond strengths of denture base-repair materials to minimize recurrent failure rate. Use microtensile bond strength (muTBS) testing to evaluate the interfacial bonding strength of 6 commercial denture repair materials after 24-hour and 12-month soaking. Blocks of poly(methyl metacrylate) (PMMA) and Triad were fabricated, fractured, and repaired. Twenty bars (1 x 1 x 30 mm) per group were sectioned from each block parallel to the long axis and approximately 90 degrees to the resin-resin repair interface and stored before muTBS testing in a servo-hydraulic tensile-testing machine. Intact PMMA and Triad bars that had been soaked for 24 hours and 12 months were tested for reference. The 24-hour repair strengths for PMMA ranged from 52% to 84% of original strength. Soaking for 12 months resulted in a 20% decrease in strength for the PMMA control. The 12-month repair strengths for PMMA ranged from 43% to 74% of the 12-month soaked material strength. Triad repair tested 35% of original strength after soaking for 24 hours. Permabond (cyanoacrylate) to PMMA tested 47% of original strength after 24 hours of soaking and 26% of the 12-month soaked material strength. Permabond to Triad tested 30% of original strength after 24 hours of soaking. Permabond and Triad showed a 100% adhesive mode of failure. All other materials tested exhibited either an adhesive mode of failure at the denture base-repair-material interface or a complex cohesive failure within the repair-material interface. The muTBS approach can be used to analyze the resin-resin interface of repaired acrylics. The relatively small standard deviations make the muTBS approach attractive. In this study, muTBS was used to evaluate the repair strength of 6 denture repair materials enabling clinicians to make clinical judgments regarding the strongest repair bond available. PMID:17987865

  10. Effects of resin formulation and nanofiller surface treatment on the properties of experimental hybrid resin composite.

    PubMed

    Musanje, Lawrence; Ferracane, Jack L

    2004-08-01

    This study evaluated the effects of nanofiller surface treatment and resin viscosity on the early and long-term properties of experimental hybrid composites. Three resin formulations (low, medium and high viscosity) were prepared by varying the ratio of TEGDMA:UDMA:bis-GMA (47:33:16 wt%; 30:33:33 wt%; 12:33:51 wt%). Composites contained 71.3 wt% silanated strontium glass (1-3 microm) and 12.6 wt% of either silanated or unsilanated silica (OX-50; 0.04 microm). Specimens (n=10) for flexural strength, flexural modulus, fracture toughness and Knoop hardness were tested after 24 h, 1 and 6 months exposure to water at 37 degrees C. Degree of conversion (DC) was determined 24 h after photoinitiation using FTIR. Resin viscosity only had a marginal influence on the mechanical response of composites but it can be adjusted to achieve a balance between DC and mechanical properties. Adding non-bonded nanofiller to hybrid composites had no systematic effect on DC. Non-bonded nanofillers had no significant effect on the long-term properties of hybrid composites. PMID:15046897

  11. Creep on a composite resin in water.

    PubMed

    Hirano, S; Hirasawa, T

    1989-06-01

    The compressive creep test of a composite resin (0-3.5 kg/mm2 stress levels) was conducted in water for 500 h. Linear regressions were obtained between the creep strains and the compressive stress levels at various hours. It is possible to predict the creep strain of the composite from the regression when it reaches water absorbed equilibrium after 500 h. The stress of the hygroscopic expansion was calculated from the linear regressions. The maximum stress due to the hygroscopic examination of the composite was 0.74 kg/mm2 at equilibrium of the water absorbed of the composite. The linear regressions at several compressive stress levels were obtained within 30-50 hr in the strain-log time diagrams. PMID:2638964

  12. Devices using resin wafers and applications thereof

    DOEpatents

    Lin, YuPo J.; Henry, Michael P.; Snyder, Seth W.; St. Martin, Edward; Arora, Michelle; de la Garza, Linda

    2009-03-24

    Devices incorporating a thin wafer of electrically and ionically conductive porous material made by the method of introducing a mixture of a thermoplastic binder and one or more of anion exchange moieties or cation exchange moieties or mixtures thereof and/or one or more of a protein capture resin and an electrically conductive material into a mold. The mixture is subjected to temperatures in the range of from about 60.degree. C. to about 170.degree. C. at pressures in the range of from about 0 to about 500 psig for a time in the range of from about 1 to about 240 minutes to form thin wafers. Devices include electrodeionization and separative bioreactors in the production of organic and amino acids, alcohols or esters for regenerating cofactors in enzymes and microbial cells.

  13. Optimized Mechanical Behavior of Vinyl Ester Resins

    NASA Astrophysics Data System (ADS)

    Ganglani, Manisha; Torkelson, John; Carr, Stephen

    2001-03-01

    The cure (polymerization and solidification) of thermoset systems has been proposed also to involve phase separation in cases where the reactants are strongly heterogeneous. Vinyl ester (VE) resins are multi-component, thermosetting systems that are suspected of undergoing such phase separation during cure, and this work seeks to investigate this possibility and how it might affect mechanical behavior of the resulting solids. The autocatalytic equation is used to describe the cure kinetics of these systems, and it is found to work only at high levels of conversion. Mechanical behavior, as studied by tensile and fracture toughness tests, is correlated to initial cure conditions and the presence or absence of initiator and accelerator species; property optima have been established. No evidence was found for a second phase formed during polymerization, explaining why excellent physical properties are realized in these materials.

  14. Methane production using resin-wafer electrodeionization

    DOEpatents

    Snyder, Seth W; Lin, YuPo; Urgun-Demirtas, Meltem

    2014-03-25

    The present invention provides an efficient method for creating natural gas including the anaerobic digestion of biomass to form biogas, and the electrodeionization of biogas to form natural gas and carbon dioxide using a resin-wafer deionization (RW-EDI) system. The method may be further modified to include a wastewater treatment system and can include a chemical conditioning/dewatering system after the anaerobic digestion system. The RW-EDI system, which includes a cathode and an anode, can either comprise at least one pair of wafers, each a basic and acidic wafer, or at least one wafer comprising of a basic portion and an acidic portion. A final embodiment of the RW-EDI system can include only one basic wafer for creating natural gas.

  15. Antibacterial activity of resin rich plant extracts

    PubMed Central

    Shuaib, Mohd; Ali, Abuzer; Ali, Mohd; Panda, Bibhu Prasad; Ahmad, Mohd Imtiyaz

    2013-01-01

    Background: The in vitro antibacterial activity of resin rich methanolic extracts (RRMEs) of Commiphora myrrha, Operculina turpethum, and Pinus roxburghii. Materials and Methods: Different concentration were studied by agar-well diffusion method against Gram-positive (Staphylococcus aureus, Bacillus subtilis, Micrococcus luteus, Enterococcus faecalis) and Gram-negative bacterial strains (Escherichia coli, Pseudomonas aeruginosa, Salmonella typhi, Shigella dysenteriae). Results: Among all the bacterial strains tested, E. faecalis was most sensitive and S. typhi was resistant to C. myrrha and P. roxburghii. The extracts of O. turpethum were active against all tested strains in which B. subtilis and S. aureus were the most sensitive. Conclusion: This suggested that the antibacterial activity of RRMEs of O. turpethum was more than C. myrrha and P. roxburghii. This probably explains the potential of these plants against a number of infections caused by bacterial strains tested. PMID:24302834

  16. Method of continuously forming polyester resins

    SciTech Connect

    Mansour, M.L.

    1984-09-18

    A method of forming a polyester resin from dicarboxylic acid anhydrides and monoepoxides in a specially designed mixing apparatus. The mixing apparatus is a vessel having a centrally disposed vertical draft tube and a centrifugal impeller at the lower end of the draft tube. A plurality of vertical heat exchange tubes surround the draft tube. The reactants are admitted into the vessel and drawn down through the draft tube by the impeller which mixes the reactants and forces the reactants up through the heat exchange tubes. The heat exchange tube portion of the vessel acts as a plug flow reactor, and the upper and lower portions of the vessel act as a back mix reactor. As reactants are admitted into the vessel, product is drawn off from the vessel.

  17. Transfer heat in a resin sheath

    SciTech Connect

    Wharry, S.R. Jr.

    1996-02-01

    As a material of construction for heat exchangers, fluoropolymers offer a combination of low cost and performance that is difficult for other materials to match. Durable, pliable, and less brittle than glass and graphite, fluoropolymers are generally specified over those materials in heat exchangers. Fluoropolymers have also displaced certain metals, depending on their susceptibility to corrosion from aggressive chemicals. Since making their debut in shell-and-tube models more than 30 years ago, fluoropolymers have also found their way into other configurations, namely reactor coils and immersion coils. Although fluoropolymer exchangers have proven their worth, there are still obstacles to overcome. One is the bias that exists toward process equipment that is made of plastic or other synthetic resins, particularly in high-heat environments. Secondly, there is the assumption that because fluoropolymers are inherently poor conductors of heat, they are odd candidates for heat exchangers. The paper discusses the advantages of fluoropolymer use in heat exchangers.

  18. Mechanical Properties of Degraded PMR-15 Resin

    NASA Technical Reports Server (NTRS)

    Tsuji, Luis C.; McManus, Hugh L.; Bowles, Kenneth J.

    1998-01-01

    Thermo-oxidative aging produces a non-uniform degradation state in PMR-15 resin. A surface layer, usually attributed to oxidative degradation, forms. This surface layer has different properties from the inner material. A set of material tests was designed to separate the properties of the oxidized surface layer from the properties of interior material. Test specimens were aged at 316 C in either air or nitrogen, for durations of up to 800 hours. The thickness of the oxidized surface layer in air aged specimens, and the shrinkage and Coefficient of Thermal Expansion (CTE) of nitrogen aged specimens were measured directly. Four-point-bend tests were performed to determine modulus of both the oxidized surface layer and the interior material. Bimaterial strip specimens consisting of oxidized surface material and unoxidized interior material were constructed and used to determine surface layer shrinkage and CTE. Results confirm that the surface layer and core materials have substantially different properties.

  19. Resin-Transfer-Molding of a Tool Face

    NASA Technical Reports Server (NTRS)

    Fowler, Mike; Ehlers, Edward; Brainard, David; Kellermann, Charles

    2004-01-01

    A resin-transfer-molding (RTM) process has been devised for fabricating a matrix/graphite-cloth composite panel that serves as tool face for manufacturing other composite panels. Heretofore, RTM has generally been confined to resins with viscosities low enough that they can readily flow through interstices of cloth. The present process makes it possible to use a high-temperature, more-viscous resin required for the tool face. First, a release layer and then a graphite cloth are laid on a foam pattern that has the desired contour. A spring with an inside diameter of 3/8 in. (.9.5 mm) is placed along the long dimension of the pattern to act as a conduit for the resin. Springs with an inside diameter of 1/4 in. (.6.4 mm) are run off the larger lengthwise spring for distributing the resin over the tool face. A glass cloth is laid on top to act as breather. The whole layup is vacuum-bagged. Resin is mixed and made to flow under vacuum assistance to infiltrate the layup through the springs. The whole process takes less than a day, and the exposure of personnel to resin vapors is minimized.

  20. Analytical method to estimate resin cement diffusion into dentin

    NASA Astrophysics Data System (ADS)

    de Oliveira Ferraz, Larissa Cristina; Ubaldini, Adriana Lemos Mori; de Oliveira, Bruna Medeiros Bertol; Neto, Antonio Medina; Sato, Fracielle; Baesso, Mauro Luciano; Pascotto, Renata Corrêa

    2016-05-01

    This study analyzed the diffusion of two resin luting agents (resin cements) into dentin, with the aim of presenting an analytical method for estimating the thickness of the diffusion zone. Class V cavities were prepared in the buccal and lingual surfaces of molars (n=9). Indirect composite inlays were luted into the cavities with either a self-adhesive or a self-etch resin cement. The teeth were sectioned bucco-lingually and the cement-dentin interface was analyzed by using micro-Raman spectroscopy (MRS) and scanning electron microscopy. Evolution of peak intensities of the Raman bands, collected from the functional groups corresponding to the resin monomer (C–O–C, 1113 cm-1) present in the cements, and the mineral content (P–O, 961 cm-1) in dentin were sigmoid shaped functions. A Boltzmann function (BF) was then fitted to the peaks encountered at 1113 cm-1 to estimate the resin cement diffusion into dentin. The BF identified a resin cement-dentin diffusion zone of 1.8±0.4 μm for the self-adhesive cement and 2.5±0.3 μm for the self-etch cement. This analysis allowed the authors to estimate the diffusion of the resin cements into the dentin. Fitting the MRS data to the BF contributed to and is relevant for future studies of the adhesive interface.

  1. Ten-years degradation of resin-dentin bonds.

    PubMed

    Hashimoto, Masanori; Fujita, Shinichi; Nagano, Futami; Ohno, Hiroki; Endo, Kazuhiko

    2010-08-01

    The purpose of this study was to evaluate the durability of resin-dentin bonds in 10-yr water-storage testing. Resin-dentin bonded bulk specimens were prepared using six commercially available resin adhesives. The resin-dentin bonded specimens were stored in water for 24 h (control group) or for 10 yr (experimental groups). After each storage period, the specimens were sectioned to make specimen beams and then subjected to a microtensile bond test. After the bond test, fractured surfaces were examined by scanning electron microscopy (SEM). In addition, interfacial observation of silver nanoleakage was performed using the backscatter electron mode of SEM. The bond strengths of four of the six adhesive systems tested decreased significantly after 10 yr. However, no significant bond-strength reduction was recorded for the other two systems. The interfacial observations showed water tree propagation in the bonding resin layer as a typical morphological change after aging for five of the six adhesives tested. Water tree propagation may be a symptom of degradation in the resin bonding layer of resin-dentin bonds. PMID:20662915

  2. Phosphorus-containing imide resins - Modification by elastomers

    NASA Technical Reports Server (NTRS)

    Varma, I. K.; Fohlen, G. M.; Parker, J. A.; Varma, D. S.

    1984-01-01

    The syntheses and general features of addition-type maleimide resins based on bis(m-aminophenyl)phosphine oxide and tris(m-aminophenyl)phosphine oxide have been reported previously. These resins have been used to fabricate graphite cloth laminates having excellent flame resistance. These composites did not burn even in pure oxygen. However, these resins were somewhat brittle. This paper reports the modification of these phosphorus-containing resins by an amine-terminated butadiene-acrylonitrile copolymer (ATBN) and a perfluoroalkylene diaromatic amine elastomer (3F). An approximately two-fold increase in short beam shear strength and flexural strength was observed at 7 percent ATBN concentration. The tensile, flexural, and shear strengths were reduced when 18 percent ATBN was used. Anaerobic char yields of the resins at 800 C and the limiting oxygen indexes of the laminates decreased with increasing ATBN concentration. The perfluorodiamine (3F) was used with both imide resins at 6.4 percent concentration. The shear strength was doubled in the case of the bisimide with no loss of flammability characteristics. The modified trisimide laminate also had improved properties over the unmodified one. The dynamic mechanical analysis of a four-ply laminate indicated a glass transition temperature above 300 C. Scanning electron micrographs of the ATBN modified imide resins were also recorded.

  3. MODELING RESULTS FROM CESIUM ION EXCHANGE PROCESSING WITH SPHERICAL RESINS

    SciTech Connect

    Nash, C.; Hang, T.; Aleman, S.

    2011-01-03

    Ion exchange modeling was conducted at the Savannah River National Laboratory to compare the performance of two organic resins in support of Small Column Ion Exchange (SCIX). In-tank ion exchange (IX) columns are being considered for cesium removal at Hanford and the Savannah River Site (SRS). The spherical forms of resorcinol formaldehyde ion exchange resin (sRF) as well as a hypothetical spherical SuperLig{reg_sign} 644 (SL644) are evaluated for decontamination of dissolved saltcake wastes (supernates). Both SuperLig{reg_sign} and resorcinol formaldehyde resin beds can exhibit hydraulic problems in their granular (nonspherical) forms. SRS waste is generally lower in potassium and organic components than Hanford waste. Using VERSE-LC Version 7.8 along with the cesium Freundlich/Langmuir isotherms to simulate the waste decontamination in ion exchange columns, spherical SL644 was found to reduce column cycling by 50% for high-potassium supernates, but sRF performed equally well for the lowest-potassium feeds. Reduced cycling results in reduction of nitric acid (resin elution) and sodium addition (resin regeneration), therefore, significantly reducing life-cycle operational costs. These findings motivate the development of a spherical form of SL644. This work demonstrates the versatility of the ion exchange modeling to study the effects of resin characteristics on processing cycles, rates, and cold chemical consumption. The value of a resin with increased selectivity for cesium over potassium can be assessed for further development.

  4. Hand/face/neck localized pattern: sticky problems--resins.

    PubMed

    Cao, Lauren Y; Sood, Apra; Taylor, James S

    2009-07-01

    Plastic resin systems have an increasingly diverse array of applications but also induce health hazards, the most common of which are allergic and irritant contact dermatitis. Contact urticaria, pigmentary changes, and photoallergic contact dermatitis may occasionally occur. Other health effects, especially respiratory and neurologic signs and symptoms, have also been reported. These resin systems include epoxies, the most frequent synthetic resin systems to cause contact dermatitis, (meth)acrylics, polyurethanes, phenol-formaldehydes, polyesters, amino resins (melamine-formaldehydes, urea-formaldehydes), polyvinyls, polystyrenes, polyolefins, polyamides and polycarbonates. Contact dermatitis usually occurs as a result of exposure to the monomers and additives in the occupational setting, although reports from consumers, using the raw materials or end products periodically surface. Resin- and additive-induced direct contact dermatitis usually presents on the hands, fingers, and forearms, while facial, eyelid, and neck involvement may occur through indirect contact, eg, via the hands, or from airborne exposure. Patch testing with commercially available materials, and in some cases the patient's own resins, is important for diagnosis. Industrial hygiene prevention techniques are essential to reduce contact dermatitis when handling these resin systems. PMID:19580919

  5. VALIDATION FOR THE PERMANGANATE DIGESTION OF REILLEX HPQ ANION RESIN

    SciTech Connect

    Kyser, E.

    2009-09-23

    The flowsheet for the digestion of Reillex{trademark} HPQ was validated both under the traditional alkaline conditions and under strongly acidic conditions. Due to difficulty in performing a pH adjustment in the large tank where this flowsheet must be performed, the recommended digestion conditions were changed from pH 8-10 to 8 M HNO{sub 3}. Thus, no pH adjustment of the solution is required prior to performing the permanganate addition and digestion and the need to sample the digestion tank to confirm appropriate pH range for digestion may be avoided. Neutralization of the acidic digestion solution will be performed after completion of the resin digestion cycle. The amount of permanganate required for this type of resin (Reillex{trademark} HPQ) was increased from 1 kg/L resin to 4 kg/L resin to reduce the amount of residual resin solids to a minimal amount (<5%). The length of digestion time at 70 C remains unchanged at 15 hours. These parameters are not optimized but are expected to be adequate for the conditions. The flowsheet generates a significant amount of fine manganese dioxide (MnO{sub 2}) solids (1.71 kg/L resin) and involves the generation of a significant liquid volume due to the low solubility of permanganate. However, since only two batches of resin (40 L each) are expected to be digested, the total waste generated is limited.

  6. 40 CFR 63.5714 - How do I demonstrate compliance if I use filled resins?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 12 2011-07-01 2009-07-01 true How do I demonstrate compliance if I... Molding Resin and Gel Coat Operations § 63.5714 How do I demonstrate compliance if I use filled resins? (a) If you are using a filled production resin or filled tooling resin, you must demonstrate...

  7. 21 CFR 177.1460 - Melamine-formaldehyde resins in molded articles.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Melamine-formaldehyde resins in molded articles...-formaldehyde resins in molded articles. Melamine-formaldehyde resins may be safely used as the food-contact...: (a) For the purpose of this section, melamine-formaldehyde resins are those produced when 1 mole...

  8. 21 CFR 177.1460 - Melamine-formaldehyde resins in molded articles.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Melamine-formaldehyde resins in molded articles...-formaldehyde resins in molded articles. Melamine-formaldehyde resins may be safely used as the food-contact...: (a) For the purpose of this section, melamine-formaldehyde resins are those produced when 1 mole...

  9. 76 FR 3614 - Granular Polytetrafluoroethylene Resin From Japan: Final Results of Sunset Review and Revocation...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-01-20

    ... resin (``PTFE resin'') from Japan. See Initiation of Five-Year (``Sunset'') Review, 75 FR 67082... Antidumping Duty Order; Granular Polytetrafluoroethylene Resin From Japan, 53 FR 32267 (August 24, 1988). On... of Antidumping Duty Orders on Granular Polytetrafluoroethylene Resin from Italy and Japan, 70...

  10. 21 CFR 177.1460 - Melamine-formaldehyde resins in molded articles.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Melamine-formaldehyde resins in molded articles...-formaldehyde resins in molded articles. Melamine-formaldehyde resins may be safely used as the food-contact...: (a) For the purpose of this section, melamine-formaldehyde resins are those produced when 1 mole...

  11. Cryogenic compressive properties of basic epoxy resin systems

    SciTech Connect

    Markley, F.W.; Hoffman, J.A.; Muniz, D.P.

    1985-09-01

    The compressive properties of short cylindrical samples of many different epoxy resin systems have been measured at ambient temperature and at 77/sup 0/K. These are pure resin systems of known chemistry, without the inorganic fillers or fibrous reinforcements needed in final cryogenic systems. Of course, chemically incorporated modifiers such as flexibilizing resins have been included. This data should make possible inferences about cryogenic properties from molecular structures and provide specific data useful to formulators and end users. Measurements on some other plastics such as PTFE, Polyimides, and UHMWPE have been made for comparison purposes.

  12. The kinetics of fossil resin extraction from a flotation concentrate

    SciTech Connect

    Li, L.; Yu, Q.; Miller, J.D.

    1995-11-01

    The kinetics of fossil resin extraction from a flotation concentrate by heptane were investigated as a function of process variables using monosize particles. Experimental results provide for a better understanding of the refining process and the basis for subsequent design and construction of a continuous resin refining circuit. Based on the effect of process variables (particle size, stirring speed, and temperature) the resin extraction rate appears to be controlled by surface solvation phenomena. The initial extraction rate was found to be inversely proportional to the initial particle size and a kinetic model is being developed to describe the experimental results.

  13. Statistical failure analysis of adhesive resin cement bonded dental ceramics

    PubMed Central

    Wang, Yaou; Katsube, Noriko; Seghi, Robert R; Rokhlin, Stanislav I.

    2007-01-01

    The goal of this work is to quantitatively examine the effect of adhesive resin cement on the probability of crack initiation from the internal surface of ceramic dental restorations. The possible crack bridging mechanism and residual stress effect of the resin cement on the ceramic surface are examined. Based on the fracture-mechanics-based failure probability model, we predict the failure probability of glass-ceramic disks bonded to simulated dentin subjected to indentation loads. The theoretical predictions match experimental data suggesting that both resin bridging and shrinkage plays an important role and need to be considered for accurate prognostics to occur. PMID:18670583

  14. Resin flow and void formation in an autoclave cure cycle

    NASA Astrophysics Data System (ADS)

    Lionetto, Francesca; Lucia, Massimo; Dell'Anna, Riccardo; Maffezzoli, Alfonso

    2016-05-01

    A finite element (FE) model able to evaluate both the evolution of resin flow, degree of reaction and void formation during autoclave cure cycles was developed. The model was implemented using a commercial epoxy matrix widely used in aeronautic field. The FE model also included a kinetic and rheological model whose input parameters were experimentally determined by Differential Scanning Calorimetry and rheological analysis. The FE model was able to predict the evolution of degree of reaction with very good agreement with the experimental data. Moreover, the predicted resin losses were lower than 3% of the overall composite resin content.

  15. Advanced thermoset resins for fire-resistant composites

    NASA Technical Reports Server (NTRS)

    Kourtides, D. A.; Parker, J. A.

    1979-01-01

    The thermal and flammability properties of some thermoset polymers and composites are described. The processing and evaluation of composites fabricated from currently used resins and advanced fire-resistant resins are also described. Laboratory test methodology used to qualify candidate composite materials includes thermochemical characterization of the polymeric compounds and evaluation of the glass reinforced composites for flammability and smoke evolution. The use of these test methods will be discussed in comparing advanced laminating resins and composites consisting of modified epoxies, phenolics and bismaleimide, with conventional baseline materials consisting of epoxy.

  16. Microtensile bond strength of indirect resin composite to resin-coated dentin: interaction between diamond bur roughness and coating material.

    PubMed

    Kameyama, Atsushi; Oishi, Takumi; Sugawara, Toyotarou; Hirai, Yoshito

    2009-02-01

    This aim of this study was to determine the effect of type of bur and resin-coating material on microtensile bond strength (microTBS) of indirect composite to dentin. Dentin surfaces were first ground with two types of diamond bur and resin-coated using UniFil Bond (UB) or Adper Single Bond (SB), and then bonded to a resin composite disc for indirect restoration with adhesive resin cement. After storage for 24 hr in distilled water at 37 degrees C, microTBS was measured (crosshead speed 1 mm/min). When UB was applied to dentin prepared using the regular-grit diamond bur, microTBS was significantly lower than that in dentin prepared using the superfine-grit bur. In contrast, no significant difference was found between regular-grit and superfine-grit bur with SB. However, more than half of the superfine-grit specimens failed before microTBS testing. These results indicate that selection of bur type is important in improving the bond strength of adhesive resin cement between indirect resin composite and resin-coated dentin. PMID:19622875

  17. Infiltration/cure modeling of resin transfer molded composite materials using advanced fiber architectures

    NASA Technical Reports Server (NTRS)

    Loos, Alfred C.; Weideman, Mark H.; Long, Edward R., Jr.; Kranbuehl, David E.; Kinsley, Philip J.; Hart, Sean M.

    1991-01-01

    A model was developed which can be used to simulate infiltration and cure of textile composites by resin transfer molding. Fabric preforms were resin infiltrated and cured using model generated optimized one-step infiltration/cure protocols. Frequency dependent electromagnetic sensing (FDEMS) was used to monitor in situ resin infiltration and cure during processing. FDEMS measurements of infiltration time, resin viscosity, and resin degree of cure agreed well with values predicted by the simulation model. Textile composites fabricated using a one-step infiltration/cure procedure were uniformly resin impregnated and void free. Fiber volume fraction measurements by the resin digestion method compared well with values predicted using the model.

  18. Extraction chromatography of neodymium by an organophosphorous extractant supported on various polymeric resins

    SciTech Connect

    Takigawa, D.Y.

    1993-04-01

    Fifteen resins coated with dihexyl-N,N-diethylcarbamoylmethyl phosphonate (CMP) were studied for their extraction of neodymium (Nd) in 4.0 and 7.0 M nitric acid. Resin properties, such as chemical composition and physical morphology, which can influence Nd extraction as well as subsequent resin regeneration (Nd stripping), were identified. Hydrophilic or polar resins coated with CMP efficiently extracted the Nd. Resins initially washed free of residual monomer and solvent before CMP coating outperformed their untreated counterparts. The macroporous styrene-divinylbenzene hydrophobic resins that were high in surface area were less effective supports compared with hydrophilic microporous Aurorez, polybenzimidazole (PBI) and macroporous Amberlite polyacrylic resins. Only one resin, Duolite C-467, showed no measurable improvement in Nd extraction with CMP coating. CMP-coated Aurorez PBI, a microporous and hydrophilic polymeric resin with an average surface area, showed the best overall efficiency for Nd removal and resin regeneration.

  19. Low-density resin impregnated ceramic article and method for making the same

    NASA Technical Reports Server (NTRS)

    Tran, Huy K. (Inventor); Henline, William D. (Inventor); Hsu, Ming-ta S. (Inventor); Rasky, Daniel J. (Inventor); Riccitiello, Salvatore R. (Inventor)

    1997-01-01

    A low-density resin impregnated ceramic article advantageously employed as a structural ceramic ablator comprising a matrix of ceramic fibers. The fibers of the ceramic matrix are coated with an organic resin film. The organic resin can be a thermoplastic resin or a cured thermosetting resin. In one embodiment, the resin is uniformly distributed within the ceramic article. In a second embodiment, the resin is distributed so as to provide a density gradient along at least one direction of the ceramic article. The resin impregnated ceramic article is prepared by providing a matrix of ceramic fibers; immersing the matrix of ceramic fibers in a solution of a solvent and an organic resin infiltrant; and removing the solvent to form a resin film on the ceramic fibers.

  20. Comparative Evaluation of Sorption, Solubility and Microhardness of Heat Cure Polymethylmethacrylate Denture Base Resin & Flexible Denture Base Resin

    PubMed Central

    Bulbule, Nilesh; Kulkarni, Shilpa; Shah, Riddhi; Kakade, Dilip

    2014-01-01

    Aim: The aim of the study was to evaluate and compare sorption, solubility and microhardness of heat cure polymethylmethacrylate (PMMA) denture base resin and flexible (thermoplastic polyamide nylon) denture base resin. Materials and Methods: Sorption, solubility and microhardness were assessed to determine compliance with ADA Specification no. 12. Results were assessed using statistical and observational analyses. Result: All materials satisfied ADA requirements for sorption, solubility and microhardness. Heat cure PMMA showed more sorption, solubility and microhardness than flexible (thermoplastic polyamide nylon). Conclusion: Flexible (thermoplastic polyamide nylon) resin absorbs less water, is less soluble and is more flexible than PMMA. PMID:25302291

  1. Removal of radioactive materials and heavy metals from water using magnetic resin

    DOEpatents

    Kochen, Robert L.; Navratil, James D.

    1997-01-21

    Magnetic polymer resins capable of efficient removal of actinides and heavy metals from contaminated water are disclosed together with methods for making, using, and regenerating them. The resins comprise polyamine-epichlorohydrin resin beads with ferrites attached to the surfaces of the beads. Markedly improved water decontamination is demonstrated using these magnetic polymer resins of the invention in the presence of a magnetic field, as compared with water decontamination methods employing ordinary ion exchange resins or ferrites taken separately.

  2. Metabolomics reveals the origins of antimicrobial plant resins collected by honey bees.

    PubMed

    Wilson, Michael B; Spivak, Marla; Hegeman, Adrian D; Rendahl, Aaron; Cohen, Jerry D

    2013-01-01

    The deposition of antimicrobial plant resins in honey bee, Apis mellifera, nests has important physiological benefits. Resin foraging is difficult to approach experimentally because resin composition is highly variable among and between plant families, the environmental and plant-genotypic effects on resins are unknown, and resin foragers are relatively rare and often forage in unobservable tree canopies. Subsequently, little is known about the botanical origins of resins in many regions or the benefits of specific resins to bees. We used metabolomic methods as a type of environmental forensics to track individual resin forager behavior through comparisons of global resin metabolite patterns. The resin from the corbiculae of a single bee was sufficient to identify that resin's botanical source without prior knowledge of resin composition. Bees from our apiary discriminately foraged for resin from eastern cottonwood (Populus deltoides), and balsam poplar (P. balsamifera) among many available, even closely related, resinous plants. Cottonwood and balsam poplar resin composition did not show significant seasonal or regional changes in composition. Metabolomic analysis of resin from 6 North American Populus spp. and 5 hybrids revealed peaks characteristic to taxonomic nodes within Populus, while antimicrobial analysis revealed that resin from different species varied in inhibition of the bee bacterial pathogen, Paenibacillus larvae. We conclude that honey bees make discrete choices among many resinous plant species, even among closely related species. Bees also maintained fidelity to a single source during a foraging trip. Furthermore, the differential inhibition of P. larvae by Populus spp., thought to be preferential for resin collection in temperate regions, suggests that resins from closely related plant species many have different benefits to bees. PMID:24204850

  3. Metabolomics Reveals the Origins of Antimicrobial Plant Resins Collected by Honey Bees

    PubMed Central

    Wilson, Michael B.; Spivak, Marla; Hegeman, Adrian D.; Rendahl, Aaron; Cohen, Jerry D.

    2013-01-01

    The deposition of antimicrobial plant resins in honey bee, Apis mellifera, nests has important physiological benefits. Resin foraging is difficult to approach experimentally because resin composition is highly variable among and between plant families, the environmental and plant-genotypic effects on resins are unknown, and resin foragers are relatively rare and often forage in unobservable tree canopies. Subsequently, little is known about the botanical origins of resins in many regions or the benefits of specific resins to bees. We used metabolomic methods as a type of environmental forensics to track individual resin forager behavior through comparisons of global resin metabolite patterns. The resin from the corbiculae of a single bee was sufficient to identify that resin's botanical source without prior knowledge of resin composition. Bees from our apiary discriminately foraged for resin from eastern cottonwood (Populus deltoides), and balsam poplar (P. balsamifera) among many available, even closely related, resinous plants. Cottonwood and balsam poplar resin composition did not show significant seasonal or regional changes in composition. Metabolomic analysis of resin from 6 North American Populus spp. and 5 hybrids revealed peaks characteristic to taxonomic nodes within Populus, while antimicrobial analysis revealed that resin from different species varied in inhibition of the bee bacterial pathogen, Paenibacillus larvae. We conclude that honey bees make discrete choices among many resinous plant species, even among closely related species. Bees also maintained fidelity to a single source during a foraging trip. Furthermore, the differential inhibition of P. larvae by Populus spp., thought to be preferential for resin collection in temperate regions, suggests that resins from closely related plant species many have different benefits to bees. PMID:24204850

  4. Removal of radioactive materials and heavy metals from water using magnetic resin

    DOEpatents

    Kochen, R.L.; Navratil, J.D.

    1997-01-21

    Magnetic polymer resins capable of efficient removal of actinides and heavy metals from contaminated water are disclosed together with methods for making, using, and regenerating them. The resins comprise polyamine-epichlorohydrin resin beads with ferrites attached to the surfaces of the beads. Markedly improved water decontamination is demonstrated using these magnetic polymer resins of the invention in the presence of a magnetic field, as compared with water decontamination methods employing ordinary ion exchange resins or ferrites taken separately. 9 figs.

  5. Elastomer-modified phosphorus-containing imide resins

    NASA Technical Reports Server (NTRS)

    Varma, I. K.; Fohlen, G. M.; Parker, J. A. (Inventor)

    1983-01-01

    Phosphine oxide-containing polyimide resins modified by elastomers, are disclosed which have improved mechanical properties. These products are particularly useful in the production of fiber or fabric-reinforced composites or laminates.

  6. 21 CFR 173.5 - Acrylate-acrylamide resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... produced by the polymerization of acrylamide with partial hydrolysis, or by copolymerization of acrylamide... polyacrylate-acrylamide resin is produced by the polymerization and subsequent hydrolysis of acrylonitrile in...

  7. 21 CFR 173.5 - Acrylate-acrylamide resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... produced by the polymerization of acrylamide with partial hydrolysis, or by copolymerization of acrylamide... polyacrylate-acrylamide resin is produced by the polymerization and subsequent hydrolysis of acrylonitrile in...

  8. 21 CFR 173.5 - Acrylate-acrylamide resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... produced by the polymerization of acrylamide with partial hydrolysis, or by copolymerization of acrylamide... polyacrylate-acrylamide resin is produced by the polymerization and subsequent hydrolysis of acrylonitrile in...

  9. Resin Permeation Through Compressed Glass Insulation for Iter Central Solenoid

    NASA Astrophysics Data System (ADS)

    Reed, R.; Roundy, F.; Martovetsky, N.; Miller, J.; Mann, T.

    2010-04-01

    Concern has been expressed about the ability of the resin system to penetrate the compressed dry glass of the turn and layer insulation during vacuum-pressure impregnation of ITER Central Solenoid (CS) modules. The stacked pancake layers of each module result in compression loads up to 9×104 kg (100 tons) on the lowest layers of each segment. The objective of this program was to assess the effects of this compressive load on resin permeation under resin-transfer conditions and with materials identical to that expected to be used in actual coil fabrication [45-50 °C, vacuum of 133 Pa (1 torr), DGEBF/anhydride epoxy resin system, E-glass satin weave, applied pressure of 125 kPa]. The experimental conditions and materials are detailed and the permeation results presented in this paper.

  10. Quantification and Purification of Mulberry Anthocyanins With Macroporous Resins

    PubMed Central

    Liu, Xueming

    2004-01-01

    Total anthocyanins in different cultivars of mulberry were measured and a process for the industrial preparation of mulberry anthocyanins as a natural food colorant was studied. In 31 cultivars of mulberry, the total anthocyanins, calculated as cyanidin 3-glucoside, ranged from 147.68 to 2725.46 mg/L juice. Extracting and purifying with macroporous resins was found to be an efficient potential method for the industrial production of mulberry anthocyanins as a food colorant. Of six resins tested, X-5 demonstrated the best adsorbent capability for mulberry anthocyanins (91 mg/mL resin). The adsorption capacity of resins increased with the surface area and the pore radius. Residual mulberry fruit juice after extraction of pigment retained most of its nutrients, except for anthocyanins, and may provide a substrate for further processing. PMID:15577197

  11. 21 CFR 872.3820 - Root canal filling resin.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... ingredient in the device. (c) Date PMA or notice of completion of a PDP is required. A PMA or a notice of... commercial distribution before May 28, 1976. Any other root canal filling resin shall have an approved PMA...

  12. 21 CFR 872.3820 - Root canal filling resin.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... ingredient in the device. (c) Date PMA or notice of completion of a PDP is required. A PMA or a notice of... commercial distribution before May 28, 1976. Any other root canal filling resin shall have an approved PMA...

  13. Effect of surface pretreatments on resin composite bonding to PEEK.

    PubMed

    Silthampitag, Patcharawan; Chaijareenont, Pisaisit; Tattakorn, Kittipong; Banjongprasert, Chaiyasit; Takahashi, Hidekazu; Arksornnukit, Mansuang

    2016-01-01

    This study evaluated the effect of surface pretreatments on resin composite bonding to polyetheretherketone (PEEK). Four groups of surface pretreatment (no pretreatment, etched with 98% sulfuric acid, etched with piranha solution and sandblasting with 50 µm alumina) were performed on PEEK. Surface roughness, Scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) analysis were examined. Shear bond strength (SBS) and interface characteristics were also evaluated after the specimens were bonded with resin materials. Two-way ANOVA analysis revealed significance on two main effects and interactions. Tukey's multiple comparisons test showed that the SBS of resin composite on PEEK were the highest in the group etched with 98% sulfuric acid and bonded with Heliobond(®) (p<0.05). All pretreatments produced similar spectra of FTIR patterns. SEM demonstrated porosities and pitting from chemical etching, which suggested a significant influence on the adhesion between PEEK and resin materials. PMID:27477234

  14. 21 CFR 177.2490 - Polyphenylene sulfide resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...,” “Determination of the Inherent Viscosity of Polyphenylene Sulfide,” and “Analysis for Dichlorobenzene in Ryton... percent by weight of finished resin. (2) Minimum inherent viscosity: 0.13 deciliters per gram. (3)...

  15. 21 CFR 172.215 - Coumarone-indene resin.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... coumarone-indene resin may be safely used on grapefruit, lemons, limes, oranges, tangelos, and tangerines in... intended for use as a protective coating for grapefruit, lemons, limes, oranges, tangelos, and...

  16. 21 CFR 172.215 - Coumarone-indene resin.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... coumarone-indene resin may be safely used on grapefruit, lemons, limes, oranges, tangelos, and tangerines in... intended for use as a protective coating for grapefruit, lemons, limes, oranges, tangelos, and...

  17. 21 CFR 172.215 - Coumarone-indene resin.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... coumarone-indene resin may be safely used on grapefruit, lemons, limes, oranges, tangelos, and tangerines in... intended for use as a protective coating for grapefruit, lemons, limes, oranges, tangelos, and...

  18. 21 CFR 172.215 - Coumarone-indene resin.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... coumarone-indene resin may be safely used on grapefruit, lemons, limes, oranges, tangelos, and tangerines in... intended for use as a protective coating for grapefruit, lemons, limes, oranges, tangelos, and...

  19. Degradation, Fatigue, and Failure of Resin Dental Composite Materials

    SciTech Connect

    Drummond, J.L.

    2008-11-03

    The intent of this article is to review the numerous factors that affect the mechanical properties of particle- or fiber-filler-containing indirect dental resin composite materials. The focus will be on the effects of degradation due to aging in different media, mainly water and water and ethanol, cyclic loading, and mixed-mode loading on flexure strength and fracture toughness. Several selected papers will be examined in detail with respect to mixed and cyclic loading, and 3D tomography with multi-axial compression specimens. The main cause of failure, for most dental resin composites, is the breakdown of the resin matrix and/or the interface between the filler and the resin matrix. In clinical studies, it appears that failure in the first 5 years is a restoration issue (technique or material selection); after that time period, failure most often results from secondary decay.

  20. Degradation, fatigue and failure of resin dental composite materials

    PubMed Central

    Drummond, James L.

    2008-01-01

    The intent of this article is to review the numerous factors that affect the mechanical properties of particle or fiber filler containing, indirect dental resin composite materials. The focus will be on degradation due to aging in different media, mainly water and water and ethanol, cyclic loading, and mixed mode loading on the flexure strength and fracture toughness. Next several selected papers will be examined in detail with respect to mixed and cyclic loading and then an examination of 3D tomography using multiaxial compression specimens. The main cause of failure, for most dental resin composites, is the breakdown of the resin matrix and or the interface between the filler and the resin matrix. In clinical studies, it appears that failure in the first 5 years is a restoration issue (technique or material selection) and after that time period from secondary decay. PMID:18650540