Science.gov

Sample records for acid resin tulsion

  1. Evaluation of anion exchange resins Tulsion A-30 and Indion-930A by application of radioanalytical technique

    NASA Astrophysics Data System (ADS)

    Singare, P. U.

    2014-07-01

    Radioanalytical technique using 131I and 82Br was employed to evaluate organic based anion exchange resins Tulsion A-30 and Indion-930A. The evaluation was based on performance of these resins during iodide and bromide ion-isotopic exchange reactions. It was observed that for iodide ion-isotopic exchange reaction by using Tulsion A-30 resin, the values of specific reaction rate (min-1), amount of iodide ion exchanged (mmol), initial rate of iodide ion exchange (mmol/min) and log K d were 0.238, 0.477, 0.114, and 11.0, respectively, which was higher than 0.155, 0.360, 0.056, and 7.3, respectively as that obtained by using Indion-930A resins under identical experimental conditions of 40.0°C, 1.000 g of ion exchange resins and 0.003 M labeled iodide ion solution. Also at a constant temperature of 40.0°C, as the concentration of labeled iodide ion solution increases 0.001 to 0.004 M, for Tulsion A-30 resins the percentage of iodide ions exchanged increases from 59.0 to 65.1%, and from 46.4 to 48.8% for Indion-930A resins under identical experimental conditions. The identical trend was observed for both the resins during bromide ion-isotopic exchange reactions. The overall results indicate that under identical experimental conditions, Tulsion A-30 show superior performance over Indion-930A resins. The results of present experimental work have demonstrated that the radioanalytical technique used here can be successfully applied for characterization of different ion exchange resins so as to evaluate their performance under various process parameters.

  2. Phosphonic acid based exchange resins

    DOEpatents

    Horwitz, E. Philip (Naperville, IL); Alexandratos, Spiro D. (Knoxville, TN); Gatrone, Ralph C. (Naperville, IL); Chiarizia, Ronato (Oak Park, IL)

    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.

  3. 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.

  4. Phosphonic acid based ion exchange resins

    DOEpatents

    Horwitz, E. Philip (Naperville, IL); Alexandratos, Spiro D. (Knoxville, TN); Gatrone, Ralph C. (Naperville, IL); Chiarizia, Ronato (Oak Park, IL)

    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.

  5. Phosphonic acid based ion exchange resins

    DOEpatents

    Horwitz, E. Philip (Naperville, IL); Alexandratos, Spiro D. (Knoxville, TN); Gatrone, Ralph C. (Naperville, IL); Chiarizia, Ronato (Oak Park, IL)

    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.

  6. 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...

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

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...provisions of this section. (a) Acrylamide-acrylic acid resins are produced by the polymerization of acrylamide with partial hydrolysis or by the copolymerization of acrylamide and acrylic acid. (b) The acrylamide-acrylic acid resins contain less...

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

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...provisions of this section. (a) Acrylamide-acrylic acid resins are produced by the polymerization of acrylamide with partial hydrolysis or by the copolymerization of acrylamide and acrylic acid. (b) The acrylamide-acrylic acid resins contain less...

  9. 21 CFR 176.110 - Acrylamide-acrylic acid resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...provisions of this section. (a) Acrylamide-acrylic acid resins are produced by the polymerization of acrylamide with partial hydrolysis or by the copolymerization of acrylamide and acrylic acid. (b) The acrylamide-acrylic acid resins contain less...

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

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...provisions of this section. (a) Acrylamide-acrylic acid resins are produced by the polymerization of acrylamide with partial hydrolysis or by the copolymerization of acrylamide and acrylic acid. (b) The acrylamide-acrylic acid resins contain less...

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

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...provisions of this section. (a) Acrylamide-acrylic acid resins are produced by the polymerization of acrylamide with partial hydrolysis or by the copolymerization of acrylamide and acrylic acid. (b) The acrylamide-acrylic acid resins contain less...

  12. 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...

  13. 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...

  14. 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...

  15. 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...

  16. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 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...

  17. 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...

  18. 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...

  19. 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...

  20. 21 CFR 175.260 - Partial phosphoric acid esters of polyester resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...false Partial phosphoric acid esters of polyester resins. 175.260 Section 175.260...260 Partial phosphoric acid esters of polyester resins. Partial phosphoric acid esters of polyester resins identified in this section...

  1. 21 CFR 175.260 - Partial phosphoric acid esters of polyester resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...true Partial phosphoric acid esters of polyester resins. 175.260 Section 175.260...260 Partial phosphoric acid esters of polyester resins. Partial phosphoric acid esters of polyester resins identified in this section...

  2. 21 CFR 175.260 - Partial phosphoric acid esters of polyester resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...false Partial phosphoric acid esters of polyester resins. 175.260 Section 175.260...260 Partial phosphoric acid esters of polyester resins. Partial phosphoric acid esters of polyester resins identified in this section...

  3. 21 CFR 175.260 - Partial phosphoric acid esters of polyester resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...false Partial phosphoric acid esters of polyester resins. 175.260 Section 175.260...260 Partial phosphoric acid esters of polyester resins. Partial phosphoric acid esters of polyester resins identified in this section...

  4. 21 CFR 175.260 - Partial phosphoric acid esters of polyester resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...false Partial phosphoric acid esters of polyester resins. 175.260 Section 175.260...260 Partial phosphoric acid esters of polyester resins. Partial phosphoric acid esters of polyester resins identified in this section...

  5. Chelating ion exchange with macroreticular hydroxamic acid resins

    SciTech Connect

    Phillips, R.J.

    1980-01-01

    The synthesis, reactions, and analytical applications of hydroxamic acids, including chelating resins with this functional group, are reviewed. A procedure for attaching N-phenyl hydroxamic acid groups to Amberlite XAD-4 is described. The extraction of 20 metal ions from 2 M hydrochloric acid by this resin is discussed. Conditions for the quantitative extraction and back-extraction of 9 ions are reported. Results are compared with work on solvent extraction with N-phenylbenzohydroxamic acid. Procedures for attaching N-methyl and N-unsubstituted hydroxamic acid groups to Amberlite XAD-4 are described. The N-phenyl, N-methyl, and N-unsubstituted hydroxamic acid resins are compared with respect to metal-ion complexation. The scope of applications for hydroxamic acid resins is investigated by studying the extraction of 19 metal ions as a function of pH. The resins are especially suitable for the extraction of zirconium(IV), titanium(IV), and uranium(IV) from strongly acidic solution. Aluminum(III) is separated from calcium and phosphate by extraction at pH 4. The use of the resins for the purification of reagents, concentration of trace constituents, and chromatographic separation is demonstrated.

  6. 21 CFR 175.260 - Partial phosphoric acid esters of polyester resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... resins are prepared by the reaction of trimellitic anhydride with 2,2-dimethyl-1,3-propanediol followed by reaction of the resin thus produced with phosphoric acid anhydride to produce a resin having...

  7. Biomimetic remineralization of resin-bonded acid-etched dentin.

    PubMed

    Tay, F R; Pashley, D H

    2009-08-01

    Degradation of denuded collagen within adhesive resin-infiltrated dentin is a pertinent problem in dentin bonding. A biomimetic remineralization scheme that incorporates non-classic crystallization pathways of fluidic amorphous nanoprecursors and mesoscopic transformation has been successful in remineralizing resin-free, acid-etched dentin, with evidence of intrafibrillar and interfibrillar remineralization. This study tested the hypothesis that biomimetic remineralization provides a means for remineralizing incompletely infiltrated resin-dentin interfaces created by etch-and-rinse adhesives. The remineralization medium consists of a Portland cement/simulated body fluid that includes polyacrylic acid and polyvinylphosphonic acid biomimetic analogs for amorphous calcium phosphate dimension regulation and collagen targeting. Both interfibrillar and intrafibrillar apatites became readily discernible within the hybrid layers after 2-4 months. In addition, intra-resin apatite clusters were deposited within the porosities of the adhesive resin matrices. The biomimetic remineralization scheme provides a proof-of-concept for the adoption of nanotechnology as an alternative strategy to extend the longevity of resin-dentin bonds. PMID:19734458

  8. Biomimetic Remineralization of Resin-bonded Acid-etched Dentin

    PubMed Central

    Tay, F.R.; Pashley, D.H.

    2009-01-01

    Degradation of denuded collagen within adhesive resin-infiltrated dentin is a pertinent problem in dentin bonding. A biomimetic remineralization scheme that incorporates non-classic crystallization pathways of fluidic amorphous nanoprecursors and mesoscopic transformation has been successful in remineralizing resin-free, acid-etched dentin, with evidence of intrafibrillar and interfibrillar remineralization. This study tested the hypothesis that biomimetic remineralization provides a means for remineralizing incompletely infiltrated resin-dentin interfaces created by etch-and-rinse adhesives. The remineralization medium consists of a Portland cement/simulated body fluid that includes polyacrylic acid and polyvinylphosphonic acid biomimetic analogs for amorphous calcium phosphate dimension regulation and collagen targeting. Both interfibrillar and intrafibrillar apatites became readily discernible within the hybrid layers after 2-4 months. In addition, intra-resin apatite clusters were deposited within the porosities of the adhesive resin matrices. The biomimetic remineralization scheme provides a proof-of-concept for the adoption of nanotechnology as an alternative strategy to extend the longevity of resin-dentin bonds. PMID:19734458

  9. REACTIVITY OF RESORCINOL FORMALDEHYDE RESIN WITH NITRIC ACID

    SciTech Connect

    King, W; Fernando Fondeur, F; Bill Wilmarth, B; Myra Pettis, M; Shirley Mccollum, S

    2006-06-14

    Solid-state infrared spectroscopy, differential scanning calorimetry, and elemental analysis have been used to evaluate the reactivity of resorcinol formaldehyde resin with nitric acid and characterize the solid product. Two distinct reactions were identified within the temperature range 25-55 C. The first reaction is primarily associated with resin nitration, while the second involves bulk oxidation and degradation of the polymer network leading to dissolution and off-gassing. Reaction was confirmed with nitric acid concentrations as low as 3 M at 25 C applied temperature and 0.625 M at 66 C. Although a nitrated resin product can be isolated under appropriate experimental conditions, calorimetry testing indicates no significant hazard associated with handling the dry material.

  10. Reactivity of Resorcinol Formaldehyde Resin with Nitric Acid

    SciTech Connect

    King, William D.; Fondeur, Fernando F.; Wilmarth, William R.; Pettis, Myra E.

    2005-10-25

    Solid-state infrared spectroscopy, differential scanning calorimetry, and elemental analysis have been used to evaluate the reactivity of resorcinol formaldehyde resin with nitric acid and characterize the solid product. Two distinct reactions were identified within the temperature range 25-55 C. The first reaction is primarily associated with resin nitration, while the second involves bulk oxidation and degradation of the polymer network leading to dissolution and off-gassing. The threshold conditions promoting reaction have been identified. Reaction was confirmed with nitric acid concentrations as low as 3 M at 25 C applied temperature and 0.625 M at 66 C. Although a nitrated resin product can be isolated under appropriate experimental conditions, calorimetry testing indicates no significant hazard associated with handling the dry material.

  11. Northwood Pulp Mill -Winter 1996 Resin Acids and 1994-1996 Chlorophenolic Compounds Summary Report

    E-print Network

    Estimated Daily Loading of Four Resin Acids Based on the Results of Three Laboratories 17 11 Pulp Mill#12;Northwood Pulp Mill - Winter 1996 Resin Acids and 1994-1996 Chlorophenolic Compounds Summary. METHODS 3 3.1 Effluent Samples 3 3.2 Resin Acids 4 3.2.1 Extraction Step 4 3.2.2 Derivatization Step 4 3

  12. Surface roughness of composite resins subjected to hydrochloric acid.

    PubMed

    Roque, Ana Carolina Cabral; Bohner, Lauren Oliveira Lima; de Godoi, Ana Paula Terossi; Colucci, Vivian; Corona, Silmara Aparecida Milori; Catirse, Alma Blásida Concepción Elizaur Benitez

    2015-01-01

    The purpose of this study was to determine the influence of hydrochloric acid on surface roughness of composite resins subjected to brushing. Sixty samples measuring 2 mm thick x 6 mm diameter were prepared and used as experimental units. The study presented a 3x2 factorial design, in which the factors were composite resin (n=20), at 3 levels: microhybrid composite (Z100), nanofilled composite (FiltekTM Supreme), nanohybrid composite (Ice), and acid challenge (n=10) at 2 levels: absence and presence. Acid challenge was performed by immersion of specimens in hydrochloric acid (pH 1.2) for 1 min, 4 times per day for 7 days. The specimens not subjected to acid challenge were stored in 15 mL of artificial saliva at 37 oC. Afterwards, all specimens were submitted to abrasive challenge by a brushing cycle performed with a 200 g weight at a speed of 356 rpm, totaling 17.8 cycles. Surface roughness measurements (Ra) were performed and analyzed by ANOVA and Tukey test (p?0.05). Surface roughness values were higher in the presence (1.07±0.24) as compared with the absence of hydrochloric acid (0.72±0.04). Surface roughness values were higher for microhybrid (1.01±0.27) compared with nanofilled (0.68 ±0.09) and nanohybrid (0.48±0.15) composites when the specimens were not subjects to acid challenge. In the presence of hydrochloric acid, microhybrid (1.26±0.28) and nanofilled (1.18±0,30) composites presents higher surface roughness values compared with nanohybrid (0.77±0.15). The hydrochloric acid affected the surface roughness of composite resin subjected to brushing. PMID:26200151

  13. Differentiating diterpene resin acids using ToF-SIMS and principal component analysis: new

    E-print Network

    Wolfe, Alexander P.

    Differentiating diterpene resin acids using ToF- SIMS and principal component analysis: new tools, carboxylic acids, alcohols, and associated esters. In recent work, we demonstrated the applicability resin acid standards were considered in this preliminary study, namely abietic acid and communic acid

  14. Polystyrene sulphonic acid resins with enhanced acid strength via macromolecular self-assembly within confined nanospace

    NASA Astrophysics Data System (ADS)

    Zhang, Xiaomin; Zhao, Yaopeng; Xu, Shutao; Yang, Yan; Liu, Jia; Wei, Yingxu; Yang, Qihua

    2014-01-01

    Tightening environmental legislation is driving the chemical industries to develop efficient solid acid catalysts to replace conventional mineral acids. Polystyrene sulphonic acid resins, as some of the most important solid acid catalysts, have been widely studied. However, the influence of the morphology on their acid strength—closely related to the catalytic activity—has seldom been reported. Herein, we demonstrate that the acid strength of polystyrene sulphonic acid resins can be adjusted through their reversible morphology transformation from aggregated to swelling state, mainly driven by the formation and breakage of hydrogen bond interactions among adjacent sulphonic acid groups within the confined nanospace of hollow silica nanospheres. The hybrid solid acid catalyst demonstrates high activity and selectivity in a series of important acid-catalysed reactions. This may offer an efficient strategy to fabricate hybrid solid acid catalysts for green chemical processes.

  15. Surface and line-edge roughness in acid-breakable resin-based positive resist

    NASA Astrophysics Data System (ADS)

    Sakamizu, Toshio; Shiraishi, Hiroshi

    2003-06-01

    A positive chemical amplification resist based on acid-catalyzed fragmentation of acetal groups in its main-chain has been developed as a means for reducing line-edge roughness. The resist consists of an acid-generator, an acid-diffusion controller and an acid-breakable (AB) resin that is synthesized through a co-condensation reaction between polyphenol and aromatic multi-functional vinylether compound. The effects of the fractionation of AB resins on resin properties and line-edge roughness (LER) are evaluated. Although AB resins have wide molecular-weight distributions, the density of acetal groups in this AB resin is found to be almost constant except in the lower molecular-weight components. The resist with a fractionated resin from which such components removed provides the high resolution of 60-nm line-and-space (L/S) patterns with fairly low LER. AFM analysis shows the surface roughness (SR) for the resist with the fractionated resin is smaller than that for a resist using non-fractionated AB resin, and that the SR value is not altered throughout the range of exposure doses up to just below the beginning of dissolution. By using the fractionated AB resin, the AB resin-based resist (ABR) is capable of forming sub-100 nm L/S patterns with less than 5 nm of LER (3?).

  16. Isolation of organic acids from large volumes of water by adsorption on macroporous resins

    USGS Publications Warehouse

    Aiken, George R.

    1987-01-01

    Adsorption on synthetic macroporous resins, such as the Amberlite XAD series and Duolite A-7, is routinely used to isolate and concentrate organic acids from forge volumes of water. Samples as large as 24,500 L have been processed on site by using these resins. Two established extraction schemes using XAD-8 and Duolite A-7 resins are described. The choice of the appropriate resin and extraction scheme is dependent on the organic solutes of interest. The factors that affect resin performance, selectivity, and capacity for a particular solute are solution pH, resin surface area and pore size, and resin composition. The logistical problems of sample handling, filtration, and preservation are also discussed.

  17. Bifunctional phenyl monophosphonic/sulfonic acid ion exchange resin and process for using the same

    DOEpatents

    Alexandratos, Spiro (Knoxville, TN); Shelley, Christopher A. (Knoxville, TN); Horwitz, E. Philip (Naperville, IL); Chiarizia, Renato (Elmhurst, IL)

    2001-01-01

    A cross-linked water-insoluble ion exchange resin comprised of polymerized monomers having a phenyl ring is disclosed. A contemplated resin contains (i) polymerized phenyl ring-containing monomers having a phosphonic acid ligand linked to the phenyl ring, (ii) about 2 to about 5 millimoles per gram (mmol/g) of phosphorus as phosphonic acid ligands, and (iii) a sufficient amount of a sulfonic acid ligand such that the ratio of mmol/g of phosphonic acid to mmol/g sulfonic acid is up to 3:1. A process for removing polyvalent metal cations from aqueous solution, and a process for removing iron(III) cations from acidic copper(II) cation-containing solutions that utilize the contemplated resin or other resins are disclosed.

  18. Bifunctional phenyl monophosphonic/sulfonic acid ion exchange resin and process for using the same

    DOEpatents

    Alexandratos, Spiro (Knoxville, TN); Shelley, Christopher A. (Knoxville, TN); Horwitz, E. Philip (Naperville, IL); Chiarizia, Renato (Elmhurst, IL); Gula, Michael J. (Chicago, IL); Xue, Sui (Darien, IL); Harvey, James T. (Naperville, IL)

    2002-01-01

    A cross-linked water-insoluble ion exchange resin comprised of polymerized monomers having a phenyl ring is disclosed. A contemplated resin contains (i) polymerized phenyl ring-containing monomers having a phosphonic acid ligand linked to the phenyl ring, (ii) about 2 to about 5 millimoles per gram (mmol/g) of phosphorus as phosphonic acid ligands, and (iii) a sufficient amount of a sulfonic acid ligand such that the ratio of mmol/g of phosphonic acid to mmol/g sulfonic acid is up to 3:1. A process for removing polyvalent metal cations from aqueous solution, and a process for removing iron(III) cations from acidic copper(II) cation-containing solutions that utilize the contemplated resin or other resins are disclosed.

  19. 40 CFR 414.50 - Applicability; description of the thermosetting resins subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...Fumaric Acid Polyesters *Furan Resins Glyoxal-Urea Formaldehyde Textile Resin *Ketone-Formaldehyde Resins *Melamine Resins *Phenolic Resins *Polyacetal Resins Polyacrylamide *Polyurethane Prepolymers *Polyurethane Resins...

  20. 40 CFR 414.50 - Applicability; description of the thermosetting resins subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...Fumaric Acid Polyesters *Furan Resins Glyoxal-Urea Formaldehyde Textile Resin *Ketone-Formaldehyde Resins *Melamine Resins *Phenolic Resins *Polyacetal Resins Polyacrylamide *Polyurethane Prepolymers *Polyurethane Resins...

  1. 21 CFR 175.260 - Partial phosphoric acid esters of polyester resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... section, partial phosphoric acid esters of polyester resins are prepared by the reaction of trimellitic anhydride with 2,2-dimethyl-1,3-propanediol followed by reaction of the resin thus produced with phosphoric... characterizing the type of food and under the conditions of time and temperature characterizing the conditions...

  2. Ion-exchange selectivity of anion exchange resin modified with polystyrenesulfonic acid.

    PubMed

    Endo, Nobutaka; Ikuta, Rei; Higa, Mitsuru; Matsusaki, Koji

    2004-07-01

    In order to change the ion-exchange selectivity of anion-exchange resin, the surface of a gel-type anion exchange resin was modified with anionic polyelectrolyte, polystyrenesulfonic acid. Using this modified resin, the ion-exchange rate of nitrate was little decreased, but that of sulfate was evidently decreased. It is considered that the ion-exchange reaction of the multivalent anion is suppressed by the greater electrostatic repulsive force against the modification layer than that against the monovalent anion. Thus, this modified resin may be suitable for the selective separation of monovalent anions. The influence of the modified condition on the ion-exchange rate was examined. Furthermore, this modified resin was used to separate nitrate ions from sulfate ions in the aqueous solution. PMID:15293411

  3. Isolation of hydrophilic organic acids from water using nonionic macroporous resins

    USGS Publications Warehouse

    Aiken, G.R.; McKnight, Diane M.; Thorn, K.A.; Thurman, E.M.

    1992-01-01

    A method has been developed for the isolation of hydrophilic organic acids from aquatic environments using Amberlite* * Use of trade names in this report is for identification purposes only and does not constitute endorsement by the U.S. Geological Survey. XAD-4 resin. The method uses a two column array of XAD-8 and XAD-4 resins in series. The hydrophobic organic acids, composed primarily of aquatic fulvic acid, are removed from the sample on XAD-8, followed by the isolation of the more hydrophilic organic acids on XAD-4. For samples from a number of diverse environments, more of the dissolved organic carbon was isolated on the XAD-8 resin (23-58%) than on the XAD-4 resin (7-25%). For these samples, the hydrophilic acids have lower carbon and hydrogen contents, higher oxygen and nitrogen contents, and are lower in molecular weight than the corresponding fulvic acids. 13C NMR analyses indicate that the hydrophilic acids have a lower concentration of aromatic carbon and greater heteroaliphatic, ketone and carboxyl content than the fulvic acid. ?? 1992.

  4. Elution profiles of lanthanides with ?-hydroxyisobutyric acid by ion exchange chromatography using fine resin.

    PubMed

    Trikha, Rahul; Sharma, Bal Krishan; Sabharwal, Kanwal Nain; Prabhu, Krishan

    2015-11-01

    Experiments were carried out using a strong acid cation exchange resin with a particle size of 75-150 ?m, termed as "fine resin" in hydrogen ion form for the elution of individual lanthanides Sm, Eu, Gd, Tb, and Dy that are produced as fission products in the spent nuclear fuel and generated in the effluent during reprocessing of spent nuclear fuel. Batch experiments were carried out to study the effect of concentration of nitric acid on distribution coefficient. The distribution coefficient values for these individual lanthanides were determined in nitric acid medium in the concentration range of 0.01-4.0 N. Uptake of each individual lanthanide by resin was increased with increased nitric acid concentration from 0.01 to 0.5 N and remained similar from 0.5 to 1.0 N and decreased thereafter up to 4.0 N. Column experiments were also carried out using the same resin to study the parameters like pH of the eluent, flow rate, and resin bed height under isocratic elution conditions for eluting lanthanide elements using ?-hydroxyisobutyric acid as eluent. The results of this study have indicated the possibility for the elution of individual lanthanides. PMID:26333182

  5. Influence of a peracetic acid-based immersion on indirect composite resin.

    PubMed

    Samuel, Susana Maria Werner; Fracaro, Gisele Baggio; Collares, Fabrício Mezzomo; Leitune, Vicente Castelo Branco; Campregher, Ulisses Bastos

    2011-06-01

    The aim of this study was to evaluate the influence of immersion in a 0.2% peracetic acid-based disinfectant on the three-point flexural strength, water sorption and water solubility of an indirect composite resin. Specimens were produced according to ISO 4049:2000 specifications and were divided in two groups: Control group, with no disinfection and Disinfected group, with three 10 min immersions in the peracetic acid intercalated with 10 min immersions in sterile distilled water. All evaluations were conducted in compliance with ISO specifications. Three-point flexural strength, water sorption and solubility of indirect composite resin before and after immersion showed no statistical significant differences (p > 0.05) and met ISO standard requirements. Immersion in peracetic acid solution showed no influence in indirect composite resin tested properties. PMID:21780726

  6. Chemically modified polymeric resins for separation of cations, organic acids, and small polar moleculea by high performance liquid chromatography

    SciTech Connect

    Morris, J.B.

    1993-07-01

    This thesis is divided into 4 parts: a review, ion chromatography of metal cations on carboxylic resins, separation of hydrophilic organic acids and small polar compounds on macroporous resin columns, and use of eluent modifiers for liquid chromatographic separation of carboxylic acids using conductivity detection.

  7. Surface degradation of composite resins by acidic medicines and pH-cycling.

    PubMed

    Valinoti, Ana Carolina; Neves, Beatriz Gonçalves; da Silva, Eduardo Moreira; Maia, Lucianne Cople

    2008-01-01

    This study evaluated the effects of acidic medicines (Dimetapp and Claritin), under pH-cycling conditions, on the surface degradation of four composite resins (microhybrid: TPH, Concept, Opallis and Nanofilled: Supreme). Thirty disc-shaped specimens ([symbol: see text] = 5.0 mm/thickness = 2.0 mm) of each composite were randomly assigned to 3 groups (n = 10): a control and two experimental groups, according to the acidic medicines evaluated. The specimens were finished and polished with aluminum oxide discs, and the surface roughness was measured by using a profilometer. After the specimens were submitted to a pH-cycling regimen and immersion in acidic medicines for 12 days, the surface roughness was measured again. Two specimens for each material and group were analyzed by scanning electron microscopy (SEM) before and after pH-cycling. Data were analyzed by the Student's-t test, ANOVA, Duncan's multiple range test and paired t-test (alpha=0.05). Significant increase in roughness was found only for TPH in the control group and TPH and Supreme immersed in Claritin (p<0.05). SEM analyses showed that the 4 composite resins underwent erosion and surface degradation after being subjected to the experimental conditions. In conclusion, although the roughness was slightly affected, the pH-cycling and acidic medicines caused surface degradation of the composite resins evaluated. Titratable acidity seemed to play a more crucial role on surface degradation of composite resins than pH. PMID:19089257

  8. SURFACE DEGRADATION OF COMPOSITE RESINS BY ACIDIC MEDICINES AND pH-CYCLING

    PubMed Central

    Valinoti, Ana Carolina; Neves, Beatriz Gonçalves; da Silva, Eduardo Moreira; Maia, Lucianne Cople

    2008-01-01

    This study evaluated the effects of acidic medicines (Dimetapp® and Claritin®), under pH-cycling conditions, on the surface degradation of four composite resins (microhybrid: TPH, Concept, Opallis and Nanofilled: Supreme). Thirty disc-shaped specimens (Ø = 5.0 mm / thickness = 2.0 mm) of each composite were randomly assigned to 3 groups (n = 10): a control and two experimental groups, according to the acidic medicines evaluated. The specimens were finished and polished with aluminum oxide discs, and the surface roughness was measured by using a profilometer. After the specimens were submitted to a pH-cycling regimen and immersion in acidic medicines for 12 days, the surface roughness was measured again. Two specimens for each material and group were analyzed by scanning electron microscopy (SEM) before and after pH-cycling. Data were analyzed by the Student's-t test, ANOVA, Duncan's multiple range test and paired t-test (?=0.05). Significant increase in roughness was found only for TPH in the control group and TPH and Supreme immersed in Claritin® (p<0.05). SEM analyses showed that the 4 composite resins underwent erosion and surface degradation after being subjected to the experimental conditions. In conclusion, although the roughness was slightly affected, the pH-cycling and acidic medicines caused surface degradation of the composite resins evaluated. Titratable acidity seemed to play a more crucial role on surface degradation of composite resins than pH. PMID:19089257

  9. Exposure to wood dust, resin acids, and volatile organic compounds during production of wood pellets.

    PubMed

    Hagström, Katja; Axelsson, Sara; Arvidsson, Helena; Bryngelsson, Ing-Liss; Lundholm, Cecilia; Eriksson, Kåre

    2008-05-01

    The main aim of this study was to investigate exposure to airborne substances that are potentially harmful to health during the production of wood pellets, including wood dust, monoterpenes, and resin acids, and as an indicator of diesel exhaust nitrogen dioxide. In addition, area measurements were taken to assess background exposure levels of these substances, volatile organic compounds (VOCs), and carbon monoxide. Measurements were taken at four wood pellet production plants from May 2004 to April 2005. Forty-four workers participated in the study, and a total of 68 personal measurements were taken to determine personal exposure to wood dust (inhalable and total dust), resin acids, monoterpenes, and nitrogen dioxide. In addition, 42 measurements of nitrogen dioxide and 71 measurements of total dust, resin acids, monoterpenes, VOCs, and carbon monoxide were taken to quantify their indoor area concentrations. Personal exposure levels to wood dust were high, and a third of the measured levels of inhalable dust exceeded the Swedish occupational exposure limit (OEL) of 2 mg/m3. Parallel measurements of inhalable and total dust indicated that the former were, on average, 3.2 times higher than the latter. The data indicate that workers at the plants are exposed to significant amounts of the resin acid 7-oxodehydroabietic acid in the air, an observation that has not been recorded previously at wood processing and handling plants. The study also found evidence of exposure to dehydroabietic acid, and exposure levels for resin acids approached 74% of the British OEL for colophony, set at 50 microg/m3. Personal exposure levels to monoterpenes and nitrogen dioxide were low. Area sampling measurements indicated that aldehydes and terpenes were the most abundant VOCs, suggesting that measuring personal exposure to aldehydes might be of interest. Carbon monoxide levels were under the detection limit in all area measurements. High wood dust exposure levels are likely to have implications for worker health; therefore, it is important to reduce exposure to wood dust in this industry. PMID:18322870

  10. Tape-stripping as a method for measuring dermal exposure to resin acids during wood pellet production.

    PubMed

    Eriksson, Kåre; Hagström, Katja; Axelsson, Sara; Nylander-French, Leena

    2008-03-01

    The purpose of this study was to develop a sensitive and specific method for quantifying dermal exposure to the resin acids 7-oxodehydroabietic acid (7-OXO), dehydroabietic acid (DHAA), abietic acid (AA), and pimaric acid (PA). In addition the method was evaluated in occupational settings during production of wood pellets. Tape-strips were spiked with the substances to evaluate the recovery of the acids from the tape. The removal efficiency of the tape was assessed by tape-stripping a specified area on a glass plate spiked with resin acids. The recovery of the acids from human skin in vivo was evaluated by applying acids in methanol onto the skin of volunteers. Occupational dermal exposure to the resin acids was assessed by tape-stripping the skin of workers involved in the production of wood pellets. The resin acids were analyzed by liquid chromatography mass spectrometry (LC-MS). The limit of detection was 15 pg (7-OXO), 150 pg (DHAA), 285 pg (AA) and 471 pg (PA) per injection. The recovery from spiked tapes was in general 100%. The removal efficiency of the tape was 48-101%. Recovery tests from human skin in vivo showed a mean recovery of 27%. Quantifiable amounts of resin acids were observed on four different skin areas with an increase in exposure during a work shift. This study shows that occupational dermal exposure to resin acids can be assessed by tape-stripping and quantified by LC-MS. PMID:18392277

  11. 21 CFR 175.260 - Partial phosphoric acid esters of polyester resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Partial phosphoric acid esters of polyester resins. 175.260 Section 175.260 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: ADHESIVES...

  12. 21 CFR 175.260 - Partial phosphoric acid esters of polyester resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Partial phosphoric acid esters of polyester resins. 175.260 Section 175.260 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: ADHESIVES...

  13. 21 CFR 175.260 - Partial phosphoric acid esters of polyester resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Partial phosphoric acid esters of polyester resins. 175.260 Section 175.260 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: ADHESIVES...

  14. A method for the production of weakly acidic cation exchange resins

    NASA Astrophysics Data System (ADS)

    Heller, H.; Werner, F.; Mitschker, A.; Diehl, H. V.; Schaefer, A.

    1991-12-01

    The invention relates to a nonpolluting method for the production of weakly acidic cation exchange resins by saponification of cross-linked acrylonitrile bead polymers, with an alkaline saponification agent at elevated temperature, according to which method the bead polymer and alkaline saponification agent are jointly added only at elevated temperature.

  15. Crypthophilic Acids A, B, and C: Resin Glycosides from Aerial Parts of Scrophularia crypthophila

    E-print Network

    Rüedi, Peter

    Crypthophilic Acids A, B, and C: Resin Glycosides from Aerial Parts of Scrophularia crypthophilaVed October 16, 2006 The water-soluble part of the methanolic extract from the aerial parts of Scrophularia, taxonomically unrelated family (Scrophulariaceae). In the flora of Turkey, the genus Scrophularia is represented

  16. Kinetics of Ethyl Acetate Synthesis Catalyzed by Acidic Resins

    ERIC Educational Resources Information Center

    Antunes, Bruno M.; Cardoso, Simao P.; Silva, Carlos M.; Portugal, Ines

    2011-01-01

    A low-cost experiment to carry out the second-order reversible reaction of acetic acid esterification with ethanol to produce ethyl acetate is presented to illustrate concepts of kinetics and reactor modeling. The reaction is performed in a batch reactor, and the acetic acid concentration is measured by acid-base titration versus time. The…

  17. Acute effects of chlorinated resin acid exposure on juvenile rainbow trout, Oncorhynchus mykiss

    SciTech Connect

    Kennedy, C.J.; Sweeting, R.M.; Farrell, A.P.; McKeown, B.A.; Johansen, J.A.

    1995-06-01

    The effects of an acute exposure to either 14-monochlorodehydroabietic acid (MCDHAA) or 12,14-dichlorodehydroabietic acid (DCDHAA) were examined in juvenile rainbow trout, Oncorhynchus mykiss. The experimentally determined 96-h LC50 values (and their 95% confidence limits) were 1.03 (0.72, 1.48) and 0.91 (0.70, 1.21) mg/L, for MCDHAA and DCDHAA, respectively. To measure effects on several biochemical parameters, swimming performance, and disease resistance, juvenile trout were exposed for 24 h to sublethal concentrations of one or the other resin acid in an intermittent-flow respirometer. Hematocrit, plasma lactate, and liver protein were significantly affected by exposure to the highest dose (80% of the 96-h LC50 value) of either of the resin acids. Plasma cortisol levels were 14- and 3-fold higher than were controls. Resistance to infection by Aeromonas salmonicida was significantly reduced; the cumulative percent mortalities due to furunculosis in fish exposed to MCDHAA or DCDHAA reached 20 and 26%, respectively. Swimming performance, measured as critical swimming speed (mean values 6.32 {+-} 0.20 and 5.93 {+-} 0.15 body lengths per second for MCDHAA and DCDHAA, respectively), was not significantly affected by resin acid exposure.

  18. 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...

  19. 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...

  20. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...accordance with the following prescribed conditions: (a) The additive is produced by polymerization of acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the greater part of the polymer being composed of...

  1. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...accordance with the following prescribed conditions: (a) The additive is produced by polymerization of acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the greater part of the polymer being composed of...

  2. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...accordance with the following prescribed conditions: (a) The additive is produced by polymerization of acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the greater part of the polymer being composed of...

  3. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...accordance with the following prescribed conditions: (a) The additive is produced by polymerization of acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the greater part of the polymer being composed of...

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

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...accordance with the following prescribed conditions: (a) The additive is produced by polymerization of acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the greater part of the polymer being composed of...

  5. Screening analyses of pinosylvin stilbenes, resin acids and lignans in Norwegian conifers.

    PubMed

    Hovelstad, Hanne; Leirset, Ingebjorg; Oyaas, Karin; Fiksdahl, Anne

    2006-01-01

    The content and distribution of stilbenes and resin acids in Scots pine (Pinus sylvestris) and spruce (Picea abies), sampled in central Norway, have been examined. The contents of pinosylvin stilbenes in pine heartwood/living knots were 0.2-2/2-8 %(w/w). No stilbenes could be detected in spruce (Picea abies). The resin acid contents of pine sapwood/heartwood and knots were 1-4 and 5-10 % (w/w), respectively. Minor amounts of resin acids (<0.2/<0.04 %w/w) were identified in spruce wood/knots. The lignan content in knots of Norwegian spruce was 6.5 % (w/w). Diastereomerically pure hydroxymatairesinol (HMR, 84 % of total lignans) was readily isolated from this source since only minor quantities (2.6 % of total lignans) of the allo-HMR diastereomer was detected. Insignificant amounts of lignans were present in the sapwood. Lignans could not be detected in the sapwood or knots of Norwegian sallow (Salix caprea), birch(Betula pendula) or juniper (Juniperus communis). PMID:17962750

  6. EVALUATION OF POTENTIAL ELUANTS FOR NON-ACID ELUTION OF CESIUM FROM RESORCINOL-FORMALDEHYDE RESIN

    SciTech Connect

    Adu-Wusu, K.; Pennebaker, F.

    2010-12-22

    Small-column ion exchange (SCIX) units installed in high-level waste tanks to remove Cs-137 from highly alkaline salt solutions are among the waste treatment plans in the DOE-complex. Spherical Resorcinol-Formaldehyde (sRF) is the ion exchange resin selected for use in the Hanford Waste Treatment and Immobilization Plant (WTP). It is also the primary ion exchange material under consideration for SCIX at the Hanford site. The elution step of the multi-step ion exchange process is typically done with 0.5 M nitric acid. An acid eluant is a potential hazard in the event of a spill, leak, etc. because the high-level waste tanks are made of carbon steel. Corrosion and associated structural damage may ensue. A study has been conducted to explore non-acid elution as an alternative. Batch contact sorption equilibrium screening tests have been conducted with 36 potential non-acid eluants. The sorption tests involve equilibrating each cesium-containing eluant solution with the sRF resin for 48 hours at 25 C in a shaker oven. In the sorption tests, an eluant is deemed to have a high cesium elution potential if it minimizes cesium sorption onto the sRF resin. The top candidates (based on lowest cesium sorption distribution coefficients) include ammonium carbonate, ammonium carbonate/ammonium hydroxide, ammonium bicarbonate, rubidium carbonate, ammonium acetate, ammonium acetate/ammonium hydroxide, ammonium bicarbonate/ammonium hydroxide, calcium chloride, and magnesium chloride. A select few of the top candidate eluants from the screening tests were subjected to actual sorption (loading) and elution tests to confirm their elution ability. The actual sorption (loading) and elution tests mimicked the typical sRF-cesium ion exchange process (i.e., sorption or loading, caustic wash, water rinse, and elution) via batch contact sorption and quasi column caustic wash/water rinse/elution. The eluants tested included ammonium carbonate, ammonium acetate, calcium acetate, magnesium acetate, and nitric acid. Calcium acetate and magnesium acetate were substitutes for calcium chloride and magnesium chloride respectively due to corrosion concerns. Nitric acid was selected for benchmarking since it is the baseline cesium eluant for sRF resin. The cesium elution performance of ammonium carbonate and ammonium acetate was approximately the same as the benchmark eluant, nitric acid. Ninety-seven (97), 94, and 100% percent of the cesium sorbed or loaded were eluted by ammonium carbonate, ammonium acetate, and nitric acid was respectively. The performance of calcium acetate and magnesium acetate, on the other hand, was mediocre. Percent elution was 16 and 8 respectively.

  7. Shear bond strength of resin cement to an acid etched and a laser irradiated ceramic surface

    PubMed Central

    Motro, Pelin Fatma Karagoz; Yurdaguven, Haktan

    2013-01-01

    PURPOSE To evaluate the effects of hydrofluoric acid etching and Er,Cr:YSGG laser irradiation on the shear bond strength of resin cement to lithium disilicate ceramic. MATERIALS AND METHODS Fifty-five ceramic blocks (5 mm × 5 mm × 2 mm) were fabricated and embedded in acrylic resin. Their surfaces were finished with 1000-grit silicon carbide paper. The blocks were assigned to five groups: 1) 9.5% hydrofluoric-acid etching for 60 s; 2-4), 1.5-, 2.5-, and 6-W Er,Cr:YSGG laser applications for 60 seconds, respectively; and 5) no treatment (control). One specimen from each group was examined using scanning electron microscopy. Ceramic primer (Rely X ceramic primer) and adhesive (Adper Single Bond) were applied to the ceramic surfaces, followed by resin cement to bond the composite cylinders, and light curing. Bonded specimens were stored in distilled water at 37? for 24 hours. Shear bond strengths were determined by a universal testing machine at 1 mm/min crosshead speed. Data were analyzed using Kruskal-Wallis and Mann-Whitney U-tests (?=0.05). RESULTS Adhesion was significantly stronger in Group 2 (3.88 ± 1.94 MPa) and Group 3 (3.65 ± 1.87 MPa) than in Control group (1.95 ± 1.06 MPa), in which bonding values were lowest (P<.01). No significant difference was observed between Group 4 (3.59 ± 1.19 MPa) and Control group. Shear bond strength was highest in Group 1 (8.42 ± 1.86 MPa; P<.01). CONCLUSION Er,Cr:YSGG laser irradiation at 1.5 and 2.5 W increased shear bond strengths between ceramic and resin cement compared with untreated ceramic surfaces. Irradiation at 6 W may not be an efficient ceramic surface treatment technique. PMID:23755333

  8. 40 CFR 414.50 - Applicability; description of the thermosetting resins subcategory.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...Product groups are indicated with an asterisk (*). *Alkyd Resins Dicyanodiamide Resin *Epoxy Resins *Fumaric Acid Polyesters *Furan Resins Glyoxal-Urea Formaldehyde Textile Resin *Ketone-Formaldehyde Resins *Melamine Resins...

  9. 40 CFR 414.50 - Applicability; description of the thermosetting resins subcategory.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...Product groups are indicated with an asterisk (*). *Alkyd Resins Dicyanodiamide Resin *Epoxy Resins *Fumaric Acid Polyesters *Furan Resins Glyoxal-Urea Formaldehyde Textile Resin *Ketone-Formaldehyde Resins *Melamine Resins...

  10. Fermentation and recovery of glutamic acid from palm waste hydrolysate by Ion-exchange resin column.

    PubMed

    Das, K; Anis, M; Azemi, B M; Ismail, N

    1995-12-01

    Glutamic acid produced from palm waste hydrolysate by fermentation with Brevibacterium lactofermentum ATCC 13869 is produced with a remarkably high yield compared with that produced from pure glucose as a carbon source. The produce yield is 70 g/L with glucose, wherease, when palm waste hydrolysate is the fermentation medium in the same bioreactor under same conditions, it is 88 g/L. The higher yield may be attributed to the fact that this organism has the ability to convert sugars other than only glucose present in the hydrolysate. Bioreactor conditions most conducive for maximum production are pH 7.5, temperature of 30 degrees rmentation period of 48 h, inoculum size 6%, substrate concentration of 10 g per 100 mL, yeast extract 0.5 g per 100 mL as a suitable N source, and biotin at a concentration of 10 pg/L. Palm waste hydrolysate used in this study was prepared by enzymic saccharification of treated palm press fiber under conditions that yielded a maximum of 30 g/L total reducing sugars. Glutamic acid from fermentation broth was recovered by using a chromatographic column (5cm x 60 cm) packed with a strong ion-exchange resin. The filtered broth containing glutamic acid and other inorganic ions was fed to the fully charged column. The broth was continuously recycled at a flow rate of 50 mL/min (retention time of 55 min) until glutamic acid was fully adsorbed on the column leaving other ions in the effluent. Recovery was done by eluting with urea and sodium hydroxide for total displacement of glutamic acid from the resin. The eluent containing 88 g/L of glutamic acid was concentrated by evaporation to obtain solid crystals of the product. (c) 1995 John Wiley & Sons, Inc. PMID:18623521

  11. Citric Acid Enhanced Copper Removal by a Novel Multi-amines Decorated Resin

    PubMed Central

    Ling, Chen; Liu, Fuqiang; Pei, Zhiguo; Zhang, Xiaopeng; Wei, Mengmeng; Zhang, Yanhong; Zheng, Lirong; Zhang, Jing; Li, Aimin; Xing, Baoshan

    2015-01-01

    Cu removal by a novel multi-amines decorated resin (PAMD) from wastewater in the absence or presence of citric acid (CA) was examined. Adsorption capacity of Cu onto PAMD markedly increased by 186% to 5.07 mmol/g in the presence of CA, up to 7 times of that onto four commercial resins under the same conditions. Preloaded and kinetic studies demonstrated adsorption of [Cu-CA] complex instead of CA site-bridging and variations of adsorbate species were qualitatively illustrated. The interaction configuration was further studied with ESI-MS, FTIR, XPS and XANES characterizations. The large enhancement of Cu adsorption in Cu-CA bi-solutes systems was attributed to mechanism change from single-site to dual-sites interaction in which cationic or neutral Cu species (Cu2+ and CuHL0) coordinated with neutral amine sites and anionic complex species (CuL? and Cu2L22?) directly interacted with protonated amine sites via electrostatic attraction, and the ratio of the two interactions was approximately 0.5 for the equimolar bi-solutes system. Moreover, commonly coexisting ions in wastewaters had no obvious effect on the superior performance of PAMD. Also, Cu and CA could be recovered completely with HCl. Therefore, PAMD has a great potential to efficiently remove heavy metal ions from wastewaters in the presence of organic acids. PMID:25962970

  12. Citric Acid Enhanced Copper Removal by a Novel Multi-amines Decorated Resin

    NASA Astrophysics Data System (ADS)

    Ling, Chen; Liu, Fuqiang; Pei, Zhiguo; Zhang, Xiaopeng; Wei, Mengmeng; Zhang, Yanhong; Zheng, Lirong; Zhang, Jing; Li, Aimin; Xing, Baoshan

    2015-05-01

    Cu removal by a novel multi-amines decorated resin (PAMD) from wastewater in the absence or presence of citric acid (CA) was examined. Adsorption capacity of Cu onto PAMD markedly increased by 186% to 5.07 mmol/g in the presence of CA, up to 7 times of that onto four commercial resins under the same conditions. Preloaded and kinetic studies demonstrated adsorption of [Cu-CA] complex instead of CA site-bridging and variations of adsorbate species were qualitatively illustrated. The interaction configuration was further studied with ESI-MS, FTIR, XPS and XANES characterizations. The large enhancement of Cu adsorption in Cu-CA bi-solutes systems was attributed to mechanism change from single-site to dual-sites interaction in which cationic or neutral Cu species (Cu2+ and CuHL0) coordinated with neutral amine sites and anionic complex species (CuL- and Cu2L22-) directly interacted with protonated amine sites via electrostatic attraction, and the ratio of the two interactions was approximately 0.5 for the equimolar bi-solutes system. Moreover, commonly coexisting ions in wastewaters had no obvious effect on the superior performance of PAMD. Also, Cu and CA could be recovered completely with HCl. Therefore, PAMD has a great potential to efficiently remove heavy metal ions from wastewaters in the presence of organic acids.

  13. Self-assembly of resins and asphaltenes facilitates asphaltene dissolution by an organic acid.

    PubMed

    Hashmi, Sara M; Firoozabadi, Abbas

    2013-03-15

    Asphaltene precipitation occurs in petroleum fluids under certain unfavorable conditions, but can be controlled by tuning composition. Aromatic solvents in large quantities can prevent precipitation entirely and can dissolve already precipitated asphaltenes. Some polymeric surfactants can dissolve asphaltenes when added at much lower concentrations than required by aromatic solvents. Other dispersants can truncate asphaltene precipitation at the sub-micron length scale, creating stable colloidal asphaltene dispersants. One particular asphaltene dispersant, dodecylbenzene sulfonic acid (DBSA), can do both, namely: (1) stabilize asphaltene colloids and (2) dissolve asphaltenes to the molecular scale. Acid-base interactions are responsible for the efficiency of DBSA in dissolving asphaltenes compared to aromatic solvents. However, many details remain to be quantified regarding the action of DBSA on asphaltenes, including the effect of petroleum fluid composition. For instance, resins, naturally amphiphilic components of petroleum fluids, can associate with asphaltenes, but it is unknown whether they cooperate or compete with DBSA. Similarly, the presence of metals is known to hinder asphaltene dissolution by DBSA, but its effect on colloidal asphaltene stabilization has yet to be considered. We introduce the concepts of cooperativity and competition between petroleum fluid components and DBSA in stabilizing and dissolving asphaltenes. Notably, we find that resins cooperatively interact with DBSA in dissolving asphaltenes. We use UV-vis spectroscopy to investigate the interactions responsible for the phase transitions between unstable suspensions, stable suspensions, and molecular solutions of asphaltenes. PMID:23351475

  14. Affinity purification of the voltage-sensitive sodium channel from electroplax with resins selective for sialic acid

    SciTech Connect

    James, W.M.; Emerick, M.C.; Agnew, W.S. )

    1989-07-11

    The voltage-sensitive sodium channel present in the eel (Electrophorus electricus) has an unusually high content of sialic acid, including {alpha}-(2{yields}8)-linked polysialic acid, not found in other electroplax membrane glycopeptides. Lectins from Limax flavus (LFA) and wheat germ (WGA) proved the most effective of 11 lectin resins tried. The most selective resin was prepared from IgM antibodies against Neisseria meningitidis {alpha}-(2{yields}8)-polysialic acid which were affinity purified and coupled to Sepharose 4B. The sodium channel was found to bind to WGA, LFA, and IgM resins and was readily eluted with the appropriate soluble carbohydrates. Experiments with LFA and IgM resins demonstrated binding and unbinding rates and displacement kinetics, which suggest highly specific binding at multiple sites on the sodium channel protein. In preparative-scale purification of protein previously fractionated by anion-exchange chromatography, without stabilizing TTX, high yields were reproducibly obtained. Further, when detergent extracts were prepared from electroplax membranes fractionated by low-speed sedimentation, a single step over the IgM resin provided a 70-fold purification, yielding specific activities of 3,200 pmol of ({sup 3}H)TTX-binding sites/mg of protein and a single polypeptide of {approximately}285,000 Da on SDS-acrylamide gels. No small peptides were observed after this 5-h isolation. The authors describe a cation-dependent stabilization with millimolar levels of monovalent and micromolar levels of divalent species.

  15. Cancer chemopreventive effects and cytotoxic activities of the triterpene acids from the resin of Boswellia carteri.

    PubMed

    Akihisa, Toshihiro; Tabata, Keiichi; Banno, Norihiro; Tokuda, Harukuni; Nishimura, Reiko; Nishihara, Reiko; Nakamura, Yuji; Kimura, Yumiko; Yasukawa, Ken; Suzuki, Takashi

    2006-09-01

    Fifteen triterpene acids, viz., seven of the beta-boswellic acids (ursane-type) (1-7), two of the alpha-boswellic acids (oleanane-type) (8, 9), two of the lupeolic acids (lupane-type) (10, 11), and four of the tirucallane-type (12-14, 16), and two cembrane-type diterpenes (17, 18), isolated from the MeOH extract of the resin of Boswellia carteri (Burseraceae), together with a triterpene acid 15 (the acetyl derivative of 14), were examined for their inhibitory effects on the induction of Epstein-Barr virus early antigen (EBV-EA) by 12-O-tetradecanoylphorbol-13-acetate (TPA) in Raji cells and on activation of (+/-)-(E)-methyl-2[(E)-hydroxyimino]-5-nitro-6-methoxy-3-hexemide (NOR 1), a nitrogen oxide (NO) donor, and cytotoxic activities against three human neuroblastoma cell lines, IMR-32, NB-39, and SK-N-SH in vitro. On evaluation against the EBV-EA activation induced by TPA, seven compounds, 2, 10, 11, and 13-16, showed potent inhibitory effects on EBV-EA induction. Upon evaluation against activation of NOR 1, five compounds, 7, 13, and 14-16, showed potent inhibitory effects. Further, fifteen compounds, 1-7, 9-11, 13-15, 17, and 18, exhibited potent cytotoxic activities with IC(50) values of 4.1-82.4 muM against all of the three human neuroblastoma cells tested. PMID:16946522

  16. Recovery of nickel and cobalt from organic acid complexes: adsorption mechanisms of metal-organic complexes onto aminophosphonate chelating resin.

    PubMed

    Deepatana, A; Valix, M

    2006-09-21

    This study examined the recovery of nickel and cobalt from organic acid complexes using a chelating aminophosphonate Purolite S950 resin. These metal complexes are generated by bioleaching nickel laterite ores, a commercial nickel and cobalt mineral oxide, with heterotrophic organism and their metabolites or organic acid products. Equilibrium adsorption tests were conducted as a function of Ni and Co concentrations (15-2000 mg/L), solution pH (0.01 and 0.1 M acids) and three metabolic complexing agents (citrate, malate and lactate). It was shown that the adsorption of the various Ni- and Co-complexes on Purolite were quite low, 16-18 and 5.4-9 mg/g of resin, respectively, in comparison to the smaller nickel ions and nickel sulfate. This was attributed to the bulky organic ligands which promoted crowding effect or steric hindrance. The adsorption of these complexes was further hampered by the strong affinity of the resin to H+ ions under acidic conditions. Mechanisms of adsorption, as inferred from the fitted empirical Langmuir and Freundlich models, were correlated to the proposed steric hindrance and competitive adsorption effects. Nickel and cobalt elution from the resin were found be effective and were independent of the type of metal complexes and metal concentrations. This study demonstrated the relative challenges involved in recovering nickel and cobalt from bioleaching solutions. PMID:16698178

  17. Fixed bed adsorption of 2-naphthalenesulfonic acid from aqueous solution by composite resin.

    PubMed

    Jia, Dong M; Li, Ya P; Li, Yue J; Li, Yong G; Li, Chang H

    2014-02-01

    Adsorption behavior of the iron impregnated, weakly basic resin D301 (Fe-D301) for removal of 2-naphthalenesulfonic acid (2-NSA) from aqueous solution was studied by using a fixed-bed column. The effects of process variables such as bed height, flow rate, and coexisting ions were investigated. The results indicated that the breakpoint and exhaustion point increased with increasing bed height and decreased with increasing 2-NSA flowrate. Experimental data showed a strong fit to the Bed Depth Service Time model. The coexisting ions in the 2-NSA solution had a clear effect on the breakthrough volume. The high extent of recovery of 2-NSA with good reproducibility provided an effective method for the separation of 2-NSA by the adsorbent Fe-D301. PMID:24645539

  18. Isolation and separation of transplutonium elements from other actinides on ion exchange resins from aqueous and aqueous ethanol solutions of sulfuric acid

    SciTech Connect

    Guseva, L.I.; Tikhomirova, G.S.; Stepushkina, V.V.

    1987-11-01

    The behavior of Am, Cm, Bk, Cf, Es, and other actinides, as well as Zr, on an anion exchange resin and a cation exchange resin in aqueous and aqueous alcohol solutions of sulfuric acid was investigated as a function of the concentration of various components of the solution. It was found that the presence of alcohol in sulfuric acid solutions leads to an increase in the distribution coefficients both on cation exchange resins and on anion exchange resins. The possibility of using ion exchange resins for the concentration and separation of transplutonium elements from U, Np, Pu, Zr, and other elements that form strong complexes with sulfate ions in a wide range of sulfuric acid concentrations was demonstrated.

  19. Separation of Technetium in Nitric Acid Solution With an Extractant Impregnated Resin

    SciTech Connect

    Jei Kwon Moon; Eil Hee Lee; Chong-Hun Jung; Byung Chul Lee

    2006-07-01

    An extractant impregnated resin (EIR) was prepared by impregnation of Aliquat 336 into Amberlite XAD-4 for separation of technetium from rhodium in nitric acid solution. The prepared EIR showed high preference for rhenium (chemical analogue of technetium) over rhodium. The adsorption isotherms for rhenium were described well by Langmuir equation in both the single and multi-component systems. Maximum adsorption capacities obtained by modelling the isotherms of rhenium were 2.01 meq g{sup -1} and 1.97 meq g{sup -1} for the single and the multi-component systems, respectively. Column tests were also performed to confirm the separation efficiency of rhenium using a jacketed glass column (diam. 11 x L 150). The EIR column showed successful separation of rhenium with the breakthrough volume of about 122 BV for the breakthrough concentration of 0.08. Also the breakthrough data were modelled successfully by assuming a homogeneous diffusion model in the particle phase. The diffusivities obtained from the modelling were in the order of 10{sup -7} cm{sup 2} min{sup -1} for a rhenium. The rhenium adsorbed on the bed could be eluted with a high purity by using a nitric acid solution. (authors)

  20. Novel bioactive polyester scaffolds prepared from unsaturated resins based on isosorbide and succinic acid.

    PubMed

    Smiga-Matuszowicz, Monika; Janicki, Bartosz; Jaszcz, Katarzyna; ?ukaszczyk, Jan; Kaczmarek, Marcin; Lesiak, Marta; Siero?, Aleksander L; Simka, Wojciech; Mierzwi?ski, Maciej; Kusz, Damian

    2014-12-01

    In this study new biodegradable materials obtained by crosslinking poly(3-allyloxy-1,2-propylene succinate) (PSAGE) with oligo(isosorbide maleate) (OMIS) and small amount of methyl methacrylate were investigated. The porous scaffolds were obtained in the presence of a foaming system consisted of calcium carbonate/carboxylic acid mixture, creating in situ porous structure during crosslinking of liquid formulations. The maximum crosslinking temperature and setting time, the cured porous materials morphology as well as the effect of their porosity on mechanical properties and hydrolytic degradation process were evaluated. It was found that the kind of carboxylic acid used in the foaming system influenced compressive strength and compressive modulus of porous scaffolds. The MTS cytotoxicity assay was carried out for OMIS using hFOB1.19 cell line. OMIS resin was found to be non-toxic in wide range of concentrations. On the ground of scanning electron microscopy (SEM) observations and energy X-ray dispersive analysis (EDX) it was found that hydroxyapatite (HA) formation at the scaffolds surfaces within short period of soaking in phosphate buffer solution occurs. After 3h immersion a compact layer of HA was observed at the surface of the samples. The obtained results suggest potential applicability of resulted new porous crosslinked polymeric materials as temporary bone void fillers. PMID:25491802

  1. Evaluation of polymeric adsorbent resins for efficient detoxification of liquor generated during acid pretreatment of lignocellulosic biomass.

    PubMed

    Sandhya, Soolamkandath Variem; Kiran, Kumar; Kuttiraja, Mathiyazhakan; Preeti, Varghese Elizabeth; Sindhu, Raveendran; Vani, Sankar; Kumar, Sukumaran Rajeev; Pandey, Ashok; Binod, Parameswaran

    2013-11-01

    Production of fuel ethanol from lignocellulosic biomass conventionally includes biomass pretreatment, hydrolysis, and fermentation. The liquor generated during dilute acid pretreatment of biomass contains considerable quantities of pentose sugars as well as various degradation products of sugars and lignin, like furfural, hydroxymethyl furfural (HMF), organic acids, aldehydes and others, which are known to be inhibitory for microbial growth. This pentose rich liquor is a potent resource which can be used to produce alcohol or other value added metabolites by microbial fermentation. However, the presence of these inhibitory compounds is a major hindrance and their removal is essential for efficient utilization of this byproduct stream. In the present work, the polymeric adsorbent resins, XAD-4, XAD-7 and XAD-16 were evaluated for their ability to adsorb fermentation inhibitors like furfural and HMF from the acid pretreated liquor. These resins could remove 55-75% of furfural and 100% of HMF and more than 90% sugar remained un-adsorbed in the pretreated liquor. Desorption of furfural from stationary phase was evaluated by using ethanol and hot water. The results suggest that these polymeric resins may be used for detoxification of acid pretreatment liquor with selective removal of sugar degradation products without affecting the sugar content in the solution. PMID:24416939

  2. Effect of acidic primers on adhesive bonding of tri-n-butylborane initiated adhesive resin to alumina.

    PubMed

    Koizumi, Hiroyasu; Nakayama, Daisuke; Oba, Yusuke; Yamada, Kazuya; Matsumura, Hideo

    2010-12-01

    The present study was conducted to evaluate the effect of acidic primers on adhesive bonding to sintered alumina. Alumina disk specimens were primed with one of the following acidic materials: Acryl Bond, All Bond II Primer B, Alloy Primer, Estenia Opaque Primer, Eye Sight Opaque Primer, M.L. Primer, MR. Bond, and Super-Bond Liquid. The disks were bonded with an adhesive resin (Super-Bond) initiated with a tri-n-butylborane (TBB) derivative, and bond strengths were determined. Average bond strength before thermocycling varied from 42.9 to 44.3 MPa, whereas post-thermocycling bond strength ranged from 22.0 to 42.8 MPa. Of the nine groups assessed, reduction of bond strength after thermocycling was not significant in three: Alloy Primer, Estenia Opaque Primer, and Eye Sight Opaque Primer. It can be concluded that phosphate-based primers are recommended for bonding sintered alumina with Super-Bond resin. PMID:21206159

  3. Relative sensitivity of five benthic invertebrate species to reference toxicants and resin-acid contaminated sediments

    SciTech Connect

    Hickey, C.W.; Martin, M.L.

    1995-08-01

    Five sediment-dwelling native New Zealand freshwater invertebrate species (amphipod, Chaetocorophium c.f. lucasi; clam, Sphaerium novaezelandiae; oligochaete, Lumbriculus variegatus; tanaid, Tanais standfordi; and the burrowing mayfly, Ichthybotus hudsoni) were assessed for their suitability for sediment toxicity testing by comparison of sensitivity to reference toxicants [phenol and pentachlorophenol (PCP)] and contaminated sediments. The 96-h EC50 values at 20 C showed a greater range in test sensitivity for phenol (30-fold range) from the most sensitive test, amphipod (8.1 mg/L), to the least sensitive one, clam (243 mg/L), compared with PCP (14-fold range), with amphipod the most sensitive test species (0.13 mg/L) and tanaid the least sensitive (1.8 mg/L). Clam reburial was a more sensitive end point than was lethality for phenol (by 20-fold) and PCP (by 2.4-fold). Four of the test species, excluding the tanaid, showed good 10-d survival in reference muds ({ge}87%) but lower survival in sand sediments ({ge}79%). Bleached kraft mill sediment containing high resin-acid concentrations (total 1,900 mg/kg dry weight) showed significant reductions in amphipod survival (15%), clam reburial (30%), and oligochaete survival (17%), and reproduction (49%). Amphipods, clams, and oligochaetes were the most promising species for sublethal test development.

  4. Protic acid resin enhanced 1-butyl-3-methylimidazolium chloride pretreatment of Arundo donax Linn.

    PubMed

    You, Tingting; Zhang, Liming; Zhou, Sukun; Xu, Feng

    2014-09-01

    To improve the cellulose digestibility of energy crop Arudo donax Linn. with cost-efficient, a novel pretreatment of protic acid resin Amberlyst 35DRY catalyzed inexpensive ionic liquid (IL) 1-butyl-3-methylimidazolium chloride ([C4mim]Cl) was developed in this work. The pretreatment was performed at 160°C with [C4mim]Cl for 1.5h, followed by Amberlyst 35DRY catalyzed at 90°C for 1h. The IL-Amberlyst pretreatment was demonstrated to be effective, evidenced by the reduction in cellulose crystallinity (31.4%) and increased porosity caused by extensive swelling the undissolved biomass and partial depolymerization of the longer cellulose chain of the dissolved biomass by Amberlyst. Consequently, a higher glucose yield (92.8%) was obtained than for the single [C4mim]Cl pretreatment (42.8%) at an enzyme loading of 20 FPU/g substrate. Overall, the enhanced pretreatment was competitive by using inexpensive and recyclable IL-Amberlyst 35DRY pretreated system with shorter processing time and reduced enzyme usage. PMID:25001325

  5. Application of polymethacrylate resin as stationary phase in liquid chromatography with UV detection for C1-C7 aliphatic monocarboxylic acids and C1-C7 aliphatic monoamines.

    PubMed

    Ohta, Kazutoku; Towata, Atsuya; Ohashi, Masayoshi; Takeuchi, Toyohide

    2004-06-11

    The application of unfunctionized polymethacrylate resin (TSKgel G3000PWXL) as a stationary phase in liquid chromatography with UV detection for C1-C7 aliphatic monocarboxylic acids (formic acid, acetic acid, propionic acid, butyric acid, isovaleric acid, valeric acid, 3,3-dimethylbutyric acid, 4-methylvaleric acid, hexanoic acid, 2-methylhexanoic acid, 5-methylhexanoic acid and heptanoic acid) and C1-C7 aliphatic monoamines (methylamine, ethylamine, propylamine, isobutylamine, butylamine, isoamylamine, amylamine, 1,3-dimethylbutylamine, hexylamine, 2-heptylamine and heptylamine) was carried out. Using dilute sulfuric acid as the eluent, the TSKgel G3000PWXL, resin acted as an advanced stationary phase for these C1-C7 carboxylic acids. Excellent simultaneous separation and symmetrical peaks for these C1-C7 carboxylic acids were achieved on a TSKgel G3000PWXL column (150 mm x 6 mm i.d.) in 60 min with 0.25 mM sulfuric acid containing 1 mM 2-methylheptanoic acid at pH 3.3 as the eluent. Using dilute sodium hydroxide as the eluent, the TSKgel G3000PWXL resin also behaved as an advanced stationary phase for these C1-C7 amines. Excellent simultaneous separation and good peaks for these C1-C7 amines were achieved on the TSKgel G3000PWXL column in 60 min with 10 mM sodium hydroxide containing 0.5 mM 1-methylheptylamine at pH 11.9 as the eluent. PMID:15250419

  6. Resin-acid derivatives as potent electrostatic openers of voltage-gated K channels and suppressors of neuronal excitability

    PubMed Central

    Ottosson, Nina E; Wu, Xiongyu; Nolting, Andreas; Karlsson, Urban; Lund, Per-Eric; Ruda, Katinka; Svensson, Stefan; Konradsson, Peter; Elinder, Fredrik

    2015-01-01

    Voltage-gated ion channels generate cellular excitability, cause diseases when mutated, and act as drug targets in hyperexcitability diseases, such as epilepsy, cardiac arrhythmia and pain. Unfortunately, many patients do not satisfactorily respond to the present-day drugs. We found that the naturally occurring resin acid dehydroabietic acid (DHAA) is a potent opener of a voltage-gated K channel and thereby a potential suppressor of cellular excitability. DHAA acts via a non-traditional mechanism, by electrostatically activating the voltage-sensor domain, rather than directly targeting the ion-conducting pore domain. By systematic iterative modifications of DHAA we synthesized 71 derivatives and found 32 compounds more potent than DHAA. The most potent compound, Compound 77, is 240 times more efficient than DHAA in opening a K channel. This and other potent compounds reduced excitability in dorsal root ganglion neurons, suggesting that resin-acid derivatives can become the first members of a new family of drugs with the potential for treatment of hyperexcitability diseases. PMID:26299574

  7. Simultaneous ion-exclusion/cation-exchange chromatography of anions and cations in acid rain waters on a weakly acidic cation-exchange resin by elution with sulfosalicylic acid.

    PubMed

    Tanaka, K; Ohta, K; Haddad, P R; Fritz, J S; Miyanaga, D A; Hu, W; Hasebe, K

    2000-07-01

    A simple, selective, and sensitive method for the simultaneous determination of anions (sulfate, nitrate, and chloride) and cations (sodium, ammonium, potassium, magnesium, and calcium) in acid rain waters was developed using ion-exclusion/ cation-exchange chromatography with conductimetric detection. A weakly acidic cation-exchange resin column (Tosho TSKgel OA-PAK-A) and a sulfosalicylic acid-methanol-water eluent was used. With a mobile phase comprising 1.25 mM sulfosalicylic acid in methanol-water (7.5:92.5) at 1.2 ml/min, simultaneous separation and detection of the above anions and cations was achieved in about 30 min. Linear calibration plots of peak area versus concentration were obtained over the concentration ranges 0-1.0 mM for anions (R=0.9991) and 0-0.5 mM for cations (R=0.9994). Detection limits calculated at S/N=3 ranged from 4.2 to 14.8 ppb for the anions and from 2.4 to 12.1 ppb for the cations. The reproducibility of retention times was 0.14-0.15% relative standard deviation (RSD) for anions and 0.18-0.31% for cations, and reproducibility of chromatographic peak areas was 1.22-1.75% RSD for anions and 1.81-2.10% for cations. The method was applied successfully to the simultaneous determination of anions and cations in aerosols transported from mainland China to central Japan, as determined by a meteorological satellite data analyzer. PMID:10917435

  8. PRELIMINARY REPORT ON EVALUATION OF POTENTIAL ELUANTS FOR NON-ACID ELUTION OF CESIUM FROM RESORCINOL-FORMALDEHYDE RESIN

    SciTech Connect

    Adu-Wusu, K.; Pennebaker, F.

    2010-09-01

    Small-column ion exchange (SCIX) units installed in high-level waste tanks to remove Cs-137 from highly alkaline salt solutions are among the waste treatment plans in the DOE-complex. Spherical Resorcinol-Formaldehyde (sRF) is the ion exchange resin selected for use in the Hanford Waste Treatment and Immobilization Plant (WTP). It is also the primary ion exchange material under consideration for SCIX at the Hanford site. The elution step of the multi-step ion exchange process is typically done with 0.5 M nitric acid. An acid eluant is a potential hazard in the event of a spill, leak, etc. because the high-level waste tanks are made of carbon steel. Corrosion and associated structural damage may ensue. Studies are ongoing to explore non-acid elution as an alternative. Batch contact sorption equilibrium screening tests have been conducted with 36 potential non-acid eluants. The sorption tests involve equilibrating each cesium-containing eluant solution with the sRF resin for 48 hours at 25 C in a shaker oven. In the sorption tests, an eluant is deemed to have a high cesium elution potential if it minimizes cesium sorption onto the sRF resin. The top candidates (based on lowest cesium sorption distribution coefficients) include ammonium carbonate, ammonium carbonate/ammonium hydroxide, ammonium bicarbonate, rubidium carbonate, ammonium acetate, ammonium acetate/ammonium hydroxide, ammonium bicarbonate/ammonium hydroxide, calcium chloride, and magnesium chloride. The next phase of testing for this work will focus on the following down selected eluants: Ammonium carbonate, ammonium acetate, calcium acetate, magnesium acetate, nitric acid, and ammonium hydroxide. The next testing phase is a confirmation of the elution ability of the selected eluants. It will mimic a typical sRF cesium ion exchange process i.e., sorption or loading, caustic wash, water rinse, and elution via batch contact sorption and quasi column caustic wash/water rinse/elution. Due to corrosion concerns, calcium acetate and magnesium acetate will be tested instead of calcium chloride and magnesium chloride respectively. Nitric acid is for benchmarking since it is the baseline sRF eluant. The information at hand indicates ammonium hydroxide, while a weak base, may hold promise as an effective eluant. Hence, its inclusion among the eluants to be studied despite the fact that it was not tested as a stand-alone eluant earlier.

  9. Synthetic resin-bound truncated Candida antarctica lipase B for production of fatty acid alkyl esters by transesterification of corn and soybean oils with ethanol or butanol.

    PubMed

    Hughes, Stephen R; Moser, Bryan R; Robinson, Samantha; Cox, Elby J; Harmsen, Amanda J; Friesen, Jon A; Bischoff, Kenneth M; Jones, Marjorie A; Pinkelman, Rebecca; Bang, Sookie S; Tasaki, Ken; Doll, Kenneth M; Qureshi, Nasib; Liu, Siqing; Saha, Badal C; Jackson, John S; Cotta, Michael A; Rich, Joseph O; Caimi, Paolo

    2012-05-31

    A gene encoding a synthetic truncated Candida antarctica lipase B (CALB) was generated via automated PCR and expressed in Saccharomyces cerevisiae. Western blot analysis detected five truncated CALB variants, suggesting multiple translation starts from the six in-frame ATG codons. The longest open reading frame, which corresponds to amino acids 35-317 of the mature lipase, appeared to be expressed in the greatest amount. The truncated CALB was immobilized on Sepabeads® EC-EP resin and used to produce ethyl and butyl esters from crude corn oil and refined soybean oil. The yield of ethyl esters was 4-fold greater from corn oil than from soybean oil and was 36% and 50% higher, respectively, when compared to a commercially available lipase resin (Novozym 435) using the same substrates. A 5:1 (v/v) ratio of ethanol to corn oil produced 3.7-fold and 8.4-fold greater yields than ratios of 15:1 and 30:1, respectively. With corn oil, butyl ester production was 56% higher than ethyl ester production. Addition of an ionic catalytic resin step prior to the CALB resin increased yields of ethyl esters from corn oil by 53% compared to CALB resin followed by ionic resin. The results suggest resin-bound truncated CALB has potential application in biodiesel production using biocatalysts. PMID:22342374

  10. Separation of Bk(IV) and Ce(IV) from trivalent transplutonium and rare earth elements on ion exchange resins in solutions of sulfuric acid

    SciTech Connect

    Guseva, L.I.; Stepushkina, V.V.

    1987-11-01

    Th behavior of Am, Cm, Bk, Cf, Es, Ce, Eu, and Pr on an anion exchange resin and a cation exchange resin in a mixture with PbO/sub 2/ was investigated in sulfuric acid solutions. A substantial difference was detected in the distribution coefficients of Bk and Ce, on the one hand, and the remaining transplutonium and rare earth elements, on the other, associated with oxidation of the first two elements to the tetravalent state. Methods are proposed for the concentration and separation of Bk(IV) and Ce(IV) from the other transplutonium and rare earth elements on an anion exchange resin in solution of 0.01-0.25 M H/sub 2/SO/sub 4/ and a cation exchange resin in 0.75-1.0 M H/sub 2/SO/sub 4/.

  11. EVALUATION OF POTENTIAL ELUANTS FOR NON-ACID ELUTION OF CESIUM FROM SPHERICAL RESORCINOL-FORMALDEHYDE RESIN

    SciTech Connect

    Adu-Wusu, K.; Nash, C.; Pennebaker, F.

    2011-10-23

    Ion Exchange column loading and elution of cesium from spherical resorcinol-formaldehyde resin have been conducted for two potential non-acid eluants -(NH{sub 4}){sub 2}CO{sub 3} and CH{sub 3}COONH{sub 4}. The results revealed encouraging cesium elution performance. 100% elution was achieved in at most 22 hours ({approx}28 bed volumes) of elution. Elution performance was fairly high at 6 hours ({approx}8 bed volumes) of elution for some of the eluants and also practically comparable to the benchmark acid eluant (HNO{sub 3}). Hence, it is quite possible 100% percent elution will be closer to the 6th hour than the 22nd hour. Elution is generally enhanced by increasing the concentration and pH of the eluants, and combining the eluants.

  12. Esterification of oleic acid in a three-phase, fixed-bed reactor packed with a cation exchange resin catalyst.

    PubMed

    Son, Sung Mo; Kimura, Hiroko; Kusakabe, Katsuki

    2011-01-01

    Esterification of oleic acid was performed in a three-phase fixed-bed reactor with a cation exchange resin catalyst (Amberlyst-15) at high temperature, which was varied from 80 to 120 °C. The fatty acid methyl ester (FAME) yields in the fixed-bed reactor were increased with increases in the reaction temperature, methanol flow rate and bed height. Moreover, the FAME yields were higher than those obtained using a batch reactor due to an equilibrium shift toward the product that resulted from continuous evaporation of the produced water. In addition, there was no catalyst deactivation during the esterification of oleic acid. However, addition of sunflower oil to the oleic acid reduced the FAME yield obtained from simultaneous esterification and transesterification. The FAME yield was 97.5% at a reaction temperature of 100 °C in the fixed-bed with a height of 5 cm when the methanol and oleic acid feed rates were 8.6 and 9.0 mL/h, respectively. PMID:20855192

  13. Synergic Catalysis of PdCu Alloy Nanoparticles within a Macroreticular Basic Resin for Hydrogen Production from Formic Acid.

    PubMed

    Mori, Kohsuke; Tanaka, Hiromasa; Dojo, Masahiro; Yoshizawa, Kazunari; Yamashita, Hiromi

    2015-08-17

    Highly dispersed PdCu alloy nanoparticles have been successfully prepared within a macroreticular basic resin bearing ?N(CH3 )2 functional groups. This previously unappreciated combination of alloy is first proven to be responsible for the efficient production of high-purity H2 from formic acid (HCOOH) dehydrogenation for chemical hydrogen storage. By the addition of Cu, the electronically promoted Pd sites show significantly higher catalytic activity as well as a better tolerance towards CO poisoning as compared to their monometallic Pd counterparts. Experimental and DFT calculation studies revealed not only the synergic alloying effect but also cooperative action by the ?N(CH3 )2 groups within the resin play crucial roles in achieving exceptional catalytic performances. In addition to the advantages such as, facile preparation method, free of additives, recyclable without leaching of active component, and suppression of unfavorable CO formation less than 3?ppm, the present catalytic system is cost-effective because of the superior catalytic activity compared with that of well-established precious PdAg or PdAu catalysts. The present catalytic system is particularly desirable for an ideal hydrogen vector in terms of potential industrial application for fuel cells. PMID:26178687

  14. Separation and conductimetric detection of C1-C7 aliphatic monocarboxylic acids and C1-C7 aliphatic monoamines on unfunctionized polymethacrylate resin columns.

    PubMed

    Ohta, Kazutoku; Towata, Atsuya; Ohashi, Masayoshi; Takeuchi, Toyohide

    2004-06-11

    The application of unfunctionized polymethacrylate resin (TSKgel G3000PWXL) as a stationary phase in liquid chromatography with conductimetric detection for C1-C7 aliphatic monocarboxylic acids (formic acid, acetic acid, propionic acid, butyric acid, isovaleric acid, valeric acid, 3,3-dimethylbutyric acid, 4-methylvaleric acid, hexanoic acid, 2-methylhexanoic acid, 5-methylhexanoic acid and heptanoic acid) and C1-C7 aliphatic monoamines (methylamine, ethylamine, propylamine, isobutylamine, butylamine, isoamylamine, amylamine, 1,3-dimethylbutylamine, hexylamine, 2-heptylamine and heptylamine) was attempted with C8 aliphatic monocarboxylic acids (2-propylvaleric acid, 2-ethylhexanoic acid, 2-methylheptanoic acid and octanoic acid) and C8 aliphatic monoamines (1,5-dimethylhexylamine, 2-ethylhexylamine, 1-methylheptylamine and octylamine) as eluents, respectively. Using 1 mM 2-methylheptanoic acid at pH 4.0 as the eluent, excellent separation and relatively high sensitive detection for these C1-C7 carboxylic acids were achieved on a TSKgel G3000PWXL column (150 mm x 6 mm i.d.) in 60 min. Using 2 mM octylamine at pH 11.0 as the eluent, excellent separation and relatively high sensitive detection for these C1-C7 amines were also achieved on the TSKgel G3000PWXL column in 60 min. PMID:15250420

  15. Catalytic Upgrading of bio-oil using 1-octene and 1-butanol over sulfonic acid resin catalysts

    SciTech Connect

    Zhang, Zhijun; Wang, Qingwen; Tripathi, Prabhat; Pittman, Charles U.

    2011-02-04

    Raw bio-oil from fast pyrolysis of biomass must be refined before it can be used as a transporation fuel, a petroleum refinery feed or for many other fuel uses. Raw bio-oil was upgraded with the neat model olefin, 1-octene, and with 1-octene/1-butanol mixtures over sulfonic acid resin catalysts frin 80 to 150 degrees celisus in order to simultaneously lower water content and acidity and to increase hydrophobicity and heating value. Phase separation and coke formation were key factors limiting the reaction rate during upgrading with neat 1-octene although octanols were formed by 1-octene hydration along with small amounts of octyl acetates and ethers. GC-MS analysis confirmed that olefin hydration, carboxylic acid esterification, acetal formation from aldehydes and ketones and O- and C-alkylations of phenolic compounds occurred simultaneously during upgrading with 1-octene/1-butanol mixtures. Addition of 1-butanol increased olefin conversion dramatically be reducing mass transfer restraints and serving as a cosolvent or emulsifying agent. It also reacted with carboxylic acids and aldehydes/ketones to form esters, and acetals, respectively, while also serving to stabilize bio-oil during heating. 1-Butanol addition also protected the catalysts, increasing catalyst lifetime and reducing or eliminationg coking. Upgrading sharply increased ester content and decreased the amounts of levoglucosan, polyhydric alcohols and organic acids. Upgrading lowered acidity (pH value rise from 2.5 to >3.0), removed the uppleasant ordor and increased hydrocarbon solubility. Water content decreased from 37.2% to < 7.5% dramatically and calorific value increased from 12.6 MJ kg to about 30.0 MJ kg.

  16. 21 CFR 177.2500 - Polyphenylene sulfone resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... consist of basic resin produced by reacting polyphenylene sulfide with peracetic acid such that the... optional adjuvant substances required in the production of such basic resins. These optional...

  17. 21 CFR 177.2500 - Polyphenylene sulfone resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... consist of basic resin produced by reacting polyphenylene sulfide with peracetic acid such that the... optional adjuvant substances required in the production of such basic resins. These optional...

  18. 21 CFR 177.2500 - Polyphenylene sulfone resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... consist of basic resin produced by reacting polyphenylene sulfide with peracetic acid such that the... optional adjuvant substances required in the production of such basic resins. These optional...

  19. 21 CFR 177.2500 - Polyphenylene sulfone resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... consist of basic resin produced by reacting polyphenylene sulfide with peracetic acid such that the... optional adjuvant substances required in the production of such basic resins. These optional...

  20. Characterization of Group V Dubnium Homologs on DGA Extraction Chromatography Resin from Nitric and Hydrofluoric Acid Matrices

    SciTech Connect

    Despotopulos, J D; Sudowe, R

    2012-02-21

    Studies of the chemical properties of superheavy elements (SHE) pose interesting challenges due to their short half-lives and low production rates. Chemical systems must have extremely fast kinetics, fast enough kinetics to be able to examine the chemical properties of interest before the SHE decays to another nuclide. To achieve chemistry on such time scales, the chemical system must also be easily automated. Most importantly however, a chemical system must be developed which provides suitable separation and kinetics before an on-line study of a SHE can be performed. Relativistic effects make studying the chemical properties of SHEs interesting due to the impact these effects could have on the SHEs chemical properties. Relativistic effects arise when the velocity of the s orbital electrons approach the speed of light. As this velocity increases, the Bohr radius of the inner electron orbitals decreases and there is an increase in the particles mass. This contraction results in a destabilization of the energy of the outer d and f electron orbitals (5f and 6d in the case of SHE), which can cause these to expand due to their increased shielding from the nuclear charge. Another relativistic effect is the spin-orbit splitting for p, d, and f orbitals into j = 1 {+-} 1/2 states. This can lead most interestingly to a possible increased stability of element 114, which due to large spin-orbit splitting of the 7p orbital and the relativistically stabilized 7p{sub 1/2} and 7s orbital gives rise to a closed shell ground state of 7s{sup 2}7p{sub 1/2}{sup 2}. The homologs of element 105, dubnium (Db), Ta and Nb and the pseudo-homolog Pa, are well known to hydrolyze and form both neutral and non-neutral monoatomic and polyatomic species that may cause issues with extraction from a given chemical system. Early ion-exchange and solvent-extraction studies show mixed results for the behavior of Db. Some studies show Db behaving most similar to Ta, while others show it behaving somewhere between Nb and Pa. Much more recent studies have examined the properties of Db from HNO{sub 3}/HF matrices, and suggest Db forms complexes similar to those of Pa. Very little experimental work into the behavior of element 114 has been performed. Thermochromatography experiments of three atoms of element 114 indicate that the element 114 is at least as volatile as Hg, At, and element 112. Lead was shown to deposit on gold at temperatures about 1000 C higher than the atoms of element 114. Results indicate a substantially increased stability of element 114. No liquid phase studies of element 114 or its homologs (Pb, Sn, Ge) or pseudo-homologs (Hg, Cd) have been performed. Theoretical predictions indicate that element 114 is should have a much more stable +2 oxidation state and neutral state than Pb, which would result in element 114 being less reactive and less metallic than Pb. The relativistic effects on the 7p{sub 1/2} electrons are predicted to cause a diagonal relationship to be introduced into the periodic table. Therefore, 114{sup 2+} is expected to behave as if it were somewhere between Hg{sup 2+}, Cd{sup 2+}, and Pb{sup 2+}. In this work two commercially available extraction chromatography resins are evaluated, one for the separation of Db homologs and pseudo?homologs from each other as well as from potential interfering elements such as Group IV Rf homologs and actinides, and the other for separation of element 114 homologs. One resin, Eichrom's DGA resin, contains a N,N,N',N'-tetra-n-octyldiglycolamide extractant, which separates analytes based on both size and charge characteristics of the solvated metal species, coated on an inert support. The DGA resin was examined for Db chemical systems, and shows a high degree of selectivity for tri-, tetra-, and hexavalent metal ions in multiple acid matrices with fast kinetics. The other resin, Eichrom's Pb resin, contains a di-t-butylcyclohexano 18-crown-6 extractant with isodecanol solvent, which separates analytes based on steric interactions between the cavity of the crown ether and electrostatic interac

  1. Wear-resistant and electromagnetic absorbing behaviors of oleic acid post-modified ferrite-filled epoxy resin composite coating

    NASA Astrophysics Data System (ADS)

    Wang, Wenjie; Zang, Chongguang; Jiao, Qingjie

    2015-03-01

    The post-modified Mn-Zn ferrite was prepared by grafting oleic acid on the surface of Mn-Zn ferrite to inhibit magnetic nanoparticle aggregation. Fourier Transform Infrared (FT-IR) spectroscopy was used to characterize the particle surfaces. The friction and electromagnetic absorbing properties of a thin coating fabricated by dispersing ferrite into epoxy resin (EP) were investigated. The roughness of the coating and water contact angle were measured using the VEECO and water contact angle meter. Friction tests were conducted using a stainless-steel bearing ball and a Rockwell diamond tip, respectively. The complex permittivity and complex permeability of the composite coating were studied in the low frequency (10 MHz-1.5 GHz). Surface modified ferrites are found to improve magnetic particles dispersion in EP resulting in significant compatibility between inorganic and organic materials. Results also indicate that modified ferrite/EP coatings have a lower roughness average value and higher water contact angle than original ferrite/EP coatings. The enhanced tribological properties of the modified ferrite/EP coatings can be seen from the increased coefficient value. The composite coatings with modified ferrite are observed to exhibit better reflection loss compared with the coatings with original ferrite.

  2. Effect of the Acidic Dental Resin Monomer 10-methacryloyloxydecyl Dihydrogen Phosphate on Odontoblastic Differentiation of Human Dental Pulp Cells.

    PubMed

    Kim, Eun-Cheol; Park, Haejin; Lee, Sang-Im; Kim, Sun-Young

    2015-11-01

    Although 10-methacryloyloxydecyl dihydrogen phosphate (10-MDP) is frequently used as an acidic resin monomer in dental adhesives, its effect on dental pulp cells (DPCs) has been rarely reported. The purpose of this study was to examine the effects of 10-MDP on the inflammatory response and odontoblastic differentiation of DPCs at minimally toxic concentrations. We found that 10-MDP caused the release of inflammatory cytokines including NO, PGE2, iNOS, COX-2, TNF-?, IL-1?, IL-6 and IL-8 in a concentration-dependent manner. In addition, 10-MDP reduced alkaline phosphatase activity, mineralization nodule formation and mRNA expression of odontoblastic differentiation markers such as dentin sialophosphoprotein, dentin matrix protein-1, osterix and Runx2 in a concentration-dependent manner with low toxicity. In addition, 10-MDP induced activation of nuclear factor-E2-related factor 2 (Nrf2) and its target gene, haeme oxygenase-1 (HO-1). We evaluated whether the effect of 10-MDP was related to the induction of HO-1 and found that treatment with a selective inhibitor of HO-1 reversed the production of 10-MDP-mediated pro-inflammatory cytokines and the inhibition of differentiation markers. Pre-treatment with either a GSH synthesis inhibitor or antioxidants blocked 10-MDP-induced mitogen-activated protein kinases (MAPKs), Nrf2 and NF-?B pathways. Taken together, the results of this study showed that minimally toxic concentrations of 10-MDP promoted an inflammatory response and suppressed odontoblastic differentiation of DPCs by activating Nrf2-mediated HO-1 induction through MAPK and NF-?B signalling. PMID:25847254

  3. Effect of acid etching duration on tensile bond strength of composite resin bonded to erbium:yttrium-aluminium-garnet laser-prepared dentine. Preliminary study.

    PubMed

    Chousterman, M; Heysselaer, D; Dridi, S M; Bayet, F; Misset, B; Lamard, L; Peremans, A; Nyssen-Behets, C; Nammour, S

    2010-11-01

    The purpose of this study was to compare the tensile bond strength of composite resin bonded to erbium:yttrium-aluminium-garnet (Er:YAG) laser-prepared dentine after different durations of acid etching. The occlusal third of 68 human third molars was removed in order to expose the dentine surface. The teeth were randomly divided into five groups: group B (control group), prepared with bur and total etch system with 15 s acid etching [37% orthophosphoric acid (H(3)PO(4))]; group L15, laser photo-ablated dentine (200 mJ) (laser irradiation conditions: pulse duration 100 micros, air-water spray, fluence 31.45 J/ cm(2), 10 Hz, non-contact hand pieces, beam spot size 0.9 mm, irradiation speed 3 mm/s, and total irradiation time 2 x 40 s); group L30, laser prepared, laser conditioned and 30 s acid etching; group L60, laser prepared, laser conditioned and 60 s acid etching; group L90, laser prepared, laser conditioned and 90 s acid etching. A plot of composite resin was bonded onto each exposed dentine and then tested for tensile bond strength. The values obtained were statistically analysed by analysis of variance (ANOVA) coupled with the Tukey-Kramer test at the 95% level. A 90 s acid etching before bonding showed the best bonding value (P < 0.05) when compared with all the other groups including the control group. There is no significance difference between other groups, nor within each group and the control group. There was a significant increase in tensile bond strength of the samples acid etched for 90 s. PMID:19685196

  4. Phosphorus-containing bisimide resins

    NASA Technical Reports Server (NTRS)

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

    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.

  5. 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.

  6. Adsorption of humic acid by bi-functional resin JN-10 and the effect of alkali-earth metal ions on the adsorption.

    PubMed

    Wang, Jinnan; Zhou, Yang; Li, Aimin; Xu, Li

    2010-04-15

    This study investigated the adsorption of humic acid (HA) by bi-functional resin JN-10, which removed the HA more effectively than the commercial resins D-301, D-201, XAD-7, and globe active carbon F-400. The difference between the FT-IR spectroscopy and (13)C NMR analysis of JN-10 before and after it adsorbing the HA revealed that both hydrophobic interaction and electric attraction were the adsorption force for the HA. The related thermodynamic parameters exhibited that the adsorption of the HA by JN-10 was an endothermic process. The occurring of adsorption was due to the increase of entropy, and the electric attraction was also a main adsorption force. In order to investigate the influence of the molecule weight (MW) of the HA on its removal by JN-10, the HA with the MWs ranging from 2000 to 100,000 Da was divided into six fractions by ultra-filtration. The HA with a medium MW (6000-10,000 Da) was preferentially removed by JN-10 due to the synergistic effect of hydrophilicity, molecular size, and aromaticity of the HA. The adsorption capacity of JN-10 for the HA increased in the presence of low concentration of alkali-earth metal ions Ca(2+) and Mg(2+), which neutralized the negative charges of the HA, but it decreased as the concentration of these ions increased because the hydrates formed by the alkali-earth metal ions occupied the adsorption sites of the resin. PMID:20074851

  7. Di-D-fructose dianhydride-enriched products by acid ion-exchange resin-promoted caramelization of D-fructose: chemical analyses.

    PubMed

    Suárez-Pereira, Elena; Rubio, Enrique M; Pilard, Serge; Ortiz Mellet, Carmen; García Fernández, José M

    2010-02-10

    Caramelization commonly occurs when sugars, or products containing a high proportion of sugars, are heated either dry or in concentrated aqueous solutions, alone or in the presence of certain additives. Upon thermal treatment of sugars, dehydration and self-condensation reactions occur, giving rise to volatiles (principally 2-hydroxymethylfurfural, HMF), pigments (melanoidines) and oligosaccharidic material, among which di-D-fructose dianhydrides (DFAs) and glycosylated DFA derivatives of different degree of polymerization (DP) have been identified. This study reports a methodology to produce caramel-like products with a high content of DFAs and oligosaccharides thereof from commercial D-fructose based on the use of acid ion-exchange resins as caramelization promotors. The rate of formation of these compounds as a function of D-fructose concentration, catalyst proportion, temperature, catalyst nature and particle size has been investigated. The use of sulfonic acid resins allows conducting caramelization at remarkable low temperatures (70-90 degrees C) to reach conversions into DFA derivatives up to 70-80% in 1-2 h, with relative proportions of HMF < 2%.The relative abundance of individual DFA structures can be modulated by acting on the catalyst nature and reaction conditions, which offers a unique opportunity for nutritional studies of DFA-enriched products with well-defined compositions. PMID:20039676

  8. Multilayer Hydrophilic Poly(phenol-formaldehyde resin)-Coated Magnetic Graphene for Boronic Acid Immobilization as a Novel Matrix for Glycoproteome Analysis.

    PubMed

    Wang, Jiaxi; Wang, Yanan; Gao, Mingxia; Zhang, Xiangmin; Yang, Pengyuan

    2015-07-29

    Capturing glycopeptides selectively and efficiently from mixed biological samples has always been critical for comprehensive and in-depth glycoproteomics analysis, but the lack of materials with superior capture capacity and high specificity still makes it a challenge. In this work, we introduce a way first to synthesize a novel boronic-acid-functionalized magnetic graphene@phenolic-formaldehyde resin multilayer composites via a facile process. The as-prepared composites gathered excellent characters of large specific surface area and strong magnetic responsiveness of magnetic graphene, biocompatibility of resin, and enhanced affinity properties of boronic acid. Furthermore, the functional graphene composites were shown to have low detection limit (1 fmol) and good selectivity, even when the background nonglycopeptides has a concentration 100 fold higher. Additionally, enrichment efficiency of the composites was still retained after being used repeatedly (at least three times). Better yet, the practical applicability of this approach was evaluated by the enrichment of human serum with a low sample volume of 1 ?L. All the results have illustrated that the magG@PF@APB has a great potential in glycoproteome analysis of complex biological samples. PMID:26161682

  9. The physical properties of conventional and resin-modified glass-ionomer dental cements stored in saliva, proprietary acidic beverages, saline and water.

    PubMed

    McKenzie, M A; Linden, R W A; Nicholson, J W

    2003-10-01

    Specimens of three conventional and one resin-modified glass-ionomer cement were prepared for both compressive strength and biaxial flexure strength determination. They were stored either in neutral media (water, saline, unstimulated whole saliva or stimulated parotid saliva) or in acidic beverages (apple juice, orange juice or Coca-Cola) for time periods ranging from 1 day to 1 year. In neutral media, the compressive and biaxial flexural strengths of all cements studied showed similar results, with significant increases apparent in compressive strengths at 6 months and which continued to 1 year, but no significant differences between the media; and no significant differences with time for biaxial flexure strength in all media. These findings show that interactions of these cements with saliva, which are known to result in deposition of calcium and phosphate, do not affect strength. Results for specimens stored in Coca-Cola were the same as for those stored in neutral media. By contrast, in orange and apple juice specimens underwent severe erosion resulting in dissolution of the conventional glass-ionomers after 3-6 months, and/or significant loss of strength at 1-3 months. Erosion of the resin-modified glass-ionomer, Vitremer, led to a significant reduction in strength, but not in dissolution, even after 12 months. The chelating carboxylic acids in these fruit juices were assumed to be responsible for these effects. PMID:12834602

  10. Comparison of shear bond strength of composite resin to enamel surface with laser etching versus acid etching: An in vitro evaluation

    PubMed Central

    Hoshing, Upendra A; Patil, Suvarna; Medha, Ashish; Bandekar, Siddhesh Dattatray

    2014-01-01

    Introduction: The aim of the study is in vitro evaluation of the shear bond strength of composite resin bonded to enamel which is pretreated using acid etchant and Er,Cr:Ysgg. Materials and Methods: 40 extracted human teeth were divided in two groups of 20 each (Groups A and B). In Group A, prepared surface of enamel was etched using 37% phosphoric acid (Scotchbond, 3M). In Group B, enamel was surface treated by a an Er, Cr: YSGG laser system (Waterlase MD, Biolase Technology Inc., San Clemente, CA, USA) operating at a wavelength of 2,780 nm and having a pulse duration of 140-200 microsecond with a repetition rate of 20 Hz and 40 Hz. Bonding agent ((Scotchbond Multipurpose, 3M) was applied over the test areas on 20 samples of Groups A and B each, and light cured. Composite resin (Ceram X duo Nanoceramic restorative, Densply) was applied onto the test areas as a 3 × 3 mm diameter bid, and light cured. The samples were tested for shear bond strength. Results: Mean shear bond strength for acid-etched enamel (26.41 ± 0.66MPa, range 25.155 to 27.150 MPa) was significantly higher (P < 0.01) than for laser-etched enamel (16.23 ± 0.71MPa, range 15.233 to 17.334 MPa). Conclusions: For enamel surface, mean shear bond strength of bonded composite obtained after laser etching were significantly lower than those obtained after acid etching. PMID:25125842

  11. Exposure of Atlantic salmon parr (Salmo salar) to a combination of resin acids and a water soluble fraction of diesel fuel oil: A model to investigate the chemical causes of pigmented salmon syndrome

    SciTech Connect

    Croce, B. |; Stagg, R.M.

    1997-09-01

    Pigmented salmon syndrome is a pollutant-induced hemolytic anemia and hyperbilirubinemia. As part of an investigation of this condition, S2 Atlantic salmon parr (Salmo salar) were exposed to a diesel fuel oil, water soluble fraction (WSF) in combination with a mixture of three resin acids (isopimaric, dehydroabietic, and abietic acids) in a continuous-flow freshwater system. The total nominal concentrations of resin acids in the exposure tanks were 10, 50, and 100 {micro}g/L; the diesel WSF was generated in situ and provided a mean hydrocarbon concentration of 2.0 {+-} 0.1 mg/L (n = 12) during the 9-d exposure period. Exposure to the diesel WSF alone depressed liver bilirubin UDP-glucuronosyl transferase (UDPGT) activity and induced phenol UDPGT activity. Exposure to the diesel WSF in the absence or presence of resin acids induced liver cytochrome P4501A and increased the concentrations in the plasma of the enzymes lactate dehydrogenase, alkaline phosphatase, and glutamic oxaloacetic transaminase. The combined exposure to diesel WSF with either 50 or 100 {micro}g/L total resin acid caused significant elevations in the concentrations of bilirubin in the plasma and many of these fish had yellow pigmentation on the ventral surface and around the gill arches. The results demonstrate that exposure to combinations of two groups of contaminants can result in the manifestation of toxic effects not apparent from exposure to either of these chemicals in isolation.

  12. Effect of sodium hypochlorite and peracetic acid on the surface roughness of acrylic resin polymerized by heated water for short and long cycles

    PubMed Central

    Sczepanski, Felipe; Sczepanski, Claudia Roberta Brunnquell; Berger, Sandrine Bittencourt; Consani, Rafael Leonardo Xediek; Gonini-Júnior, Alcides; Guiraldo, Ricardo Danil

    2014-01-01

    Objective: To evaluate the surface roughness of acrylic resin submitted to chemical disinfection via 1% sodium hypochlorite (NaClO) or 1% peracetic acid (C2H4O3). Materials and Methods: The disc-shaped resin specimens (30 mm diameter ×4 mm height) were polymerized by heated water using two cycles (short cycle: 1 h at 74°C and 30 min at 100°C; conventional long cycle: 9 h at 74°C). The release of substances by these specimens in water solution was also quantified. Specimens were fabricated, divided into four groups (n = 10) depending on the polymerization time and disinfectant. After polishing, the specimens were stored in distilled deionized water. Specimens were immersed in 1% NaClO or 1% C2H4O3 for 30 min, and then were immersed in distilled deionized water for 20 min. The release of C2H4O3 and NaClO was measured via visual colorimetric analysis. Roughness was measured before and after disinfection. Roughness data were subjected to two-way ANOVA and Tukey's test. Results: There was no interaction between polymerization time and disinfectant in influencing the average surface roughness (Ra, P = 0.957). Considering these factors independently, there were significant differences between short and conventional long cycles (P = 0.012), but no significant difference between the disinfectants hypochlorite and C2H4O3 (P = 0.366). Visual colorimetric analysis did not detect release of substances. Conclusion: It was concluded that there was the difference in surface roughness between short and conventional long cycles, and disinfection at acrylic resins polymerized by heated water using a short cycle modified the properties of roughness. PMID:25512737

  13. Kinetic, equilibrium and thermodynamic studies on sorption of uranium and thorium from aqueous solutions by a selective impregnated resin containing carminic acid.

    PubMed

    Rahmani-Sani, Abolfazl; Hosseini-Bandegharaei, Ahmad; Hosseini, Seyyed-Hossein; Kharghani, Keivan; Zarei, Hossein; Rastegar, Ayoob

    2015-04-01

    In this work, the removal of uranium and thorium ions from aqueous solutions was studied by solid-liquid extraction using an advantageous extractant-impregnated resin (EIR) prepared by loading carminic acid (CA) onto Amberlite XAD-16 resin beads. Batch sorption experiments using CA/XAD-16 beads for the removal of U(VI) and Th(IV) ions were carried out as a function of several parameters, like equilibration time, metal ion concentration, etc. The equilibrium data obtained from the sorption experiments were adjusted to the Langmuir isotherm model and the calculated maximum sorption capacities in terms of monolayer sorption were in agreement with those obtained from the experiments. The experimental data on the sorption behavior of both metal ions onto the EIR beads fitted well in both Bangham and intra-particle diffusion kinetic models, indicating that the intra-particle diffusion is the rate-controlling step. The thermodynamic studies at different temperatures revealed the feasibility and the spontaneous nature of the sorption process for both uranium and thorium ions. PMID:25576783

  14. 21 CFR 177.2500 - Polyphenylene sulfone resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... polyphenylene sulfide with peracetic acid such that the finished resins meet the specifications set forth in... production of such basic resins. These optional adjuvant substances may include substances permitted for...

  15. Variability and determinants of wood dust and resin acid exposure during wood pellet production: measurement strategies and bias in assessing exposure-response relationships.

    PubMed

    Hagström, Katja; Lundholm, Cecilia; Eriksson, Kare; Liljelind, Ingrid

    2008-11-01

    Production of wood pellets is a relatively new and expanding industry in which the exposure profiles differ from those in other wood-processing industries like carpentries and sawmills where there are lower levels of wood dust. Sixty-eight personal exposure measurements of wood dust (inhalable and total dust) and resin acids were collected for 44 participants at four production plants located in Sweden. Results were used to estimate within- and between-worker variability and to identify uniformly exposed groups and determinants of exposure. In addition, overexposure, whether the risk of the long-term mean exposure of a randomly selected worker exceeding the occupational exposure limit is acceptably low, was calculated as well as the underestimation of the exposure-response relationship (attenuation). Greater variability in exposure between work shifts than between workers was observed with the within-worker variation accounting for 57-99% of the total variance in the individual-based model. Several uniformly exposed groups were detected but were mostly associated with a between-worker variation of zero which is an underestimation of the between-worker variation but an indication of uniformly exposed groups. Cleaning was identified as a work task that increases exposure slightly; so reducing workers' exposure during this operation is advisable. The levels of wood dust were high and were found to pose unacceptable risks of overexposure at all plants for inhalable dust and at three out of four plants for total dust. These findings show that exposure to dust needs to be reduced in this industry. For resin acids, the exposure was classed as acceptable at all plants. According to an individual-based model constructed from the data, the level of attenuation was high, and thus there would be substantial bias in derived dose-response relationships. PMID:18703543

  16. Processing large-diameter poly(L-lactic acid) microfiber mesh/mesenchymal stromal cell constructs via resin embedding: an efficient histologic method.

    PubMed

    D'Alessandro, Delfo; Pertici, Gianni; Moscato, Stefania; Metelli, Maria Rita; Danti, Sabrina; Nesti, Claudia; Berrettini, Stefano; Petrini, Mario; Danti, Serena

    2014-08-01

    In this study, we performed a complete histologic analysis of constructs based on large diameter (?>100 ?m) poly-L-lactic acid (PLLA) microfibers obtained via dry-wet spinning and rat Mesenchymal Stromal Cells (rMSCs) differentiated towards the osteogenic lineage, using acrylic resin embedding. In many synthetic polymer-based microfiber meshes, ex post processability of fiber/cell constructs for histologic analysis may face deterring difficulties, leading to an incomplete investigation of the potential of these scaffolds. Indeed, while polymeric nanofiber (fiber diameter = tens of nanometers)/cell constructs can usually be embedded in common histologic media and easily sectioned, preserving the material structure and the antigenic reactivity, histologic analysis of large polymeric microfiber/cell constructs in the literature is really scant. This affects microfiber scaffolds based on FDA-approved and widely used polymers such as PLLA and its copolymers. Indeed, for such constructs, especially those with fiber diameter and fiber interspace much larger than cell size, standard histologic processing is usually inefficient due to inhomogeneous hardness and lack of cohesion between the synthetic and the biological phases under sectioning. In this study, the microfiber/MSC constructs were embedded in acrylic resin and the staining/reaction procedures were calibrated to demonstrate the possibility of successfully employing histologic methods in tissue engineering studies even in such difficult cases. We histologically investigated the main osteogenic markers and extracellular matrix molecules, such as alkaline phosphatase, osteopontin, osteocalcin, TGF-?1, Runx2, Collagen type I and the presence of amorphous, fibrillar and mineralized matrix. Biochemical tests were employed to confirm our findings. This protocol permitted efficient sectioning of the treated constructs and good penetration of the histologic reagents, thus allowing distribution and expression of almost all the tested molecules to be revealed. Our results demonstrated that it is possible to perform histologic analyses of large-diameter PLLA-based microfiber scaffold/MSC constructs that face the failure of standard histologic procedures. PMID:25029413

  17. Resin composite restorative materials.

    PubMed

    Ilie, N; Hickel, R

    2011-06-01

    This paper surveys the most important developments in resin-based dental composites and focuses on the deficits (e.g. polymerization shrinkage) and strengths of the materials and their clinical implications. Moreover, differences between composite categories, such as hybrid, nanohybrid, microfilled, packable, ormocer-based, silorane-based, polyacid-modified composites (compomers) and flowable composites are highlighted, especially in view of their mechanical behaviour. In addition to the classical dimethacrylate-based composites, special attention is given to alternative monomers, such as siloranes, ormocers or high-molecular-weight dimethacrylate monomers (e.g. dimer acid-based dimethacrylates and tricyclodecane (TCD)-urethane), analysing their advantages, behaviour and abilities. Finally, the paper attempts to establish the needs and wishes of clinicians for further development of resin-based composites. PMID:21564116

  18. On-line preconcentration with a novel alkyl phosphinic acid extraction resin coupled with inductively coupled plasma mass spectrometry for determination of trace rare earth elements in seawater.

    PubMed

    Fu, Qiang; Yang, Limin; Wang, Qiuquan

    2007-06-15

    A newly synthesized alkyl phosphinic acid resin (APAR) was used for on-line preconcentration of trace rare earth elements (REES, lanthanides including yttrium) and then determined by inductively coupled plasma mass spectrometry. REEs in seawater could be on-line concentrated on the APAR packed column (4.6mm i.d.x50mm in length), and eluted from the column with 0.5mL 0.1molL(-1) nitric acid within 30s. An enrichment factor of nearly 400 was achieved for all REEs when the seawater sample volume was 200mL, while the matrix and coexisting spectrally interfering ions such as barium, tin and antimony could be simultaneously separated. The detection limits of this proposed method for REEs were in the range from 1.43pgL(-1) of holmium to 12.7pgL(-1) of lanthanum. The recoveries of REEs were higher than 97.9%, and the precision of the relative standard deviation (R.S.D., n=6) was less than 5%. The method has been applied to the determination of soluble REEs in seawater. PMID:19071752

  19. Distributed Drug Discovery, Part 2: Global Rehearsal of Alkylating Agents for the Synthesis of Resin-Bound Unnatural Amino Acids and Virtual D3 Catalog Construction

    PubMed Central

    2008-01-01

    Distributed Drug Discovery (D3) proposes solving large drug discovery problems by breaking them into smaller units for processing at multiple sites. A key component of the synthetic and computational stages of D3 is the global rehearsal of prospective reagents and their subsequent use in the creation of virtual catalogs of molecules accessible by simple, inexpensive combinatorial chemistry. The first section of this article documents the feasibility of the synthetic component of Distributed Drug Discovery. Twenty-four alkylating agents were rehearsed in the United States, Poland, Russia, and Spain, for their utility in the synthesis of resin-bound unnatural amino acids 1, key intermediates in many combinatorial chemistry procedures. This global reagent rehearsal, coupled to virtual library generation, increases the likelihood that any member of that virtual library can be made. It facilitates the realistic integration of worldwide virtual D3 catalog computational analysis with synthesis. The second part of this article describes the creation of the first virtual D3 catalog. It reports the enumeration of 24?416 acylated unnatural amino acids 5, assembled from lists of either rehearsed or well-precedented alkylating and acylating reagents, and describes how the resulting catalog can be freely accessed, searched, and downloaded by the scientific community. PMID:19105725

  20. 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.

  1. 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.

  2. 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.

  3. 21 CFR 173.5 - Acrylate-acrylamide resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... of acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid, with... resin is produced by the polymerization and subsequent hydrolysis of acrylonitrile in a sodium...

  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. 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.

  6. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...Terpene resins consisting of polymers of beta-pinene and meeting the following specifications: Acid value less than 1; saponification number less than 1; color less than 4 on the Gardner scale as measured in 50 percent mineral spirits...

  7. Influence of air-abrasion executed with polyacrylic acid-Bioglass 45S5 on the bonding performance of a resin-modified glass ionomer cement.

    PubMed

    Sauro, Salvatore; Watson, Timothy F; Thompson, Ian; Toledano, Manuel; Nucci, Cesare; Banerjee, Avijit

    2012-04-01

    The aim of this study was to test the microtensile bond strength (?TBS), after 6 months of storage in PBS, of a resin-modified glass ionomer cement (RMGIC) bonded to dentine pretreated with Bioglass 45S5 (BAG) using various etching and air-abrasion techniques. The RMGIC (GC Fuji II LC) was applied onto differently treated dentine surfaces followed by light curing for 30 s. The specimens were cut into matchsticks with cross-sectional areas of 0.9 mm(2). The ?TBS of the specimens was measured after 24 h or 6 months of storage in PBS and the results were statistically analysed using two-way anova and the Student-Newman-Keuls test (? = 0.05). Further RMCGIC-bonded dentine specimens were used for interfacial characterization, micropermeability, and nanoleakage analyses by confocal microscopy. The RMGIC-dentine interface layer showed no water absorption after 6 months of storage in PBS except for the interdiffusion layer of the silicon carbide (SiC)-abraded/polyacrylic acid (PAA)-etched bonded dentine. The RMGIC applied onto dentine air-abraded with BAG/H(2)O only or with BAG/PAA-fluid followed by etching procedures (10% PAA gel) showed no statistically significant reduction in ?TBS after 6 months of storage in PBS. The abrasion procedures performed using BAG in combination with PAA might be a suitable strategy to enhance the bonding durability and the healing ability of RMGIC bonded to dentine. PMID:22409224

  8. K Basin Sludge Conditioning Process Testing Project Results from Test 4, ''Acid Digestion of Mixed-Bed Ion Exchange Resin''

    SciTech Connect

    Pool, K.H.; Delegard, C.H.; Schmidt, A.J.; Thornton, B.M.; Silvers, K.L.

    1999-04-02

    Approximately 73 m{sup 3} of heterogeneous solid material, ''sludge,'' (upper bound estimate, Packer 1997) have accumulated at the bottom of the K Basins in the 100 K Area of the Hanford Site. This sludge is a mixture of spent fuel element corrosion products, ion exchange materials (organic and inorganic), graphite-based gasket materials, iron and aluminum metal corrosion products, sand, and debris (Makenas et al. 1996, 1997). In addition, small amounts of polychlorinated biphenyls (PCBs) have been found. Ultimately, it is planned to transfer the K Basins sludge to the Hanford double shell tanks (DSTs). The Hanford Spent Nuclear Fuel (HSNF) project has conducted a number of evaluations to examine technology and processing alternatives to pretreat K Basin sludge to meet storage and disposal requirements. From these evaluations, chemical pretreatment has been selected to address criticality issues, reactivity, and the destruction or removal of PCBs before the K Basin sludge can be transferred to the DSTs. Chemical pretreatment, referred to as the K Basin sludge conditioning process, includes nitric acid dissolution of the sludge (with removal of acid insoluble solids), neutrons absorber addition, neutralization, and reprecipitation. Laboratory testing is being conducted by the Pacific Northwest National Laboratory (PNNL) to provide data necessary to develop the sludge conditioning process.

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

    DOEpatents

    Yamamori, Naoki (Minoo, JP); Yokoi, Junji (Nara, JP); Yoshikawa, Motoyoshi (Nara, JP)

    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.

  10. Evolution of Conifer Diterpene Synthases: Diterpene Resin Acid Biosynthesis in Lodgepole Pine and Jack Pine Involves Monofunctional and Bifunctional Diterpene Synthases1[W][OA

    PubMed Central

    Hall, Dawn E.; Zerbe, Philipp; Jancsik, Sharon; Quesada, Alfonso Lara; Dullat, Harpreet; Madilao, Lina L.; Yuen, Macaire; Bohlmann, Jörg

    2013-01-01

    Diterpene resin acids (DRAs) are major components of pine (Pinus spp.) oleoresin. They play critical roles in conifer defense against insects and pathogens and as a renewable resource for industrial bioproducts. The core structures of DRAs are formed in secondary (i.e. specialized) metabolism via cycloisomerization of geranylgeranyl diphosphate (GGPP) by diterpene synthases (diTPSs). Previously described gymnosperm diTPSs of DRA biosynthesis are bifunctional enzymes that catalyze the initial bicyclization of GGPP followed by rearrangement of a (+)-copalyl diphosphate intermediate at two discrete class II and class I active sites. In contrast, similar diterpenes of gibberellin primary (i.e. general) metabolism are produced by the consecutive activity of two monofunctional class II and class I diTPSs. Using high-throughput transcriptome sequencing, we discovered 11 diTPS from jack pine (Pinus banksiana) and lodgepole pine (Pinus contorta). Three of these were orthologous to known conifer bifunctional levopimaradiene/abietadiene synthases. Surprisingly, two sets of orthologous PbdiTPSs and PcdiTPSs were monofunctional class I enzymes that lacked functional class II active sites and converted (+)-copalyl diphosphate, but not GGPP, into isopimaradiene and pimaradiene as major products. Diterpene profiles and transcriptome sequences of lodgepole pine and jack pine are consistent with roles for these diTPSs in DRA biosynthesis. The monofunctional class I diTPSs of DRA biosynthesis form a new clade within the gymnosperm-specific TPS-d3 subfamily that evolved from bifunctional diTPS rather than monofunctional enzymes (TPS-c and TPS-e) of gibberellin metabolism. Homology modeling suggested alterations in the class I active site that may have contributed to their functional specialization relative to other conifer diTPSs. PMID:23370714

  11. 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.

  12. 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.

  13. Polyester Resin Hazards

    PubMed Central

    Bourne, L. B.; Milner, F. J. M.

    1963-01-01

    Polyester resins are being increasingly used in industry. These resins require the addition of catalysts and accelerators. The handling of polyester resin system materials may give rise to skin irritations, allergic reactions, and burns. The burns are probably due to styrene and organic peroxides. Atmospheric pollution from styrene and explosion and fire risks from organic peroxides must be prevented. Where dimethylaniline is used scrupulous cleanliness and no-touch technique must be enforced. Handling precautions are suggested. Images PMID:14014495

  14. Resin catalysts and method of preparation

    DOEpatents

    Smith, Jr., Lawrence A. (P.O. Box 34687, Houston, TX 77243)

    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.

  15. 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.

  16. 21 CFR 173.5 - Acrylate-acrylamide resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...prescribed conditions: (a) The additive consists of one of the following: (1) Acrylamide-acrylic acid resin (hydrolyzed polyacrylamide) is produced by the polymerization of acrylamide with partial hydrolysis, or by copolymerization of...

  17. 21 CFR 173.5 - Acrylate-acrylamide resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...prescribed conditions: (a) The additive consists of one of the following: (1) Acrylamide-acrylic acid resin (hydrolyzed polyacrylamide) is produced by the polymerization of acrylamide with partial hydrolysis, or by copolymerization of...

  18. 21 CFR 173.5 - Acrylate-acrylamide resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...prescribed conditions: (a) The additive consists of one of the following: (1) Acrylamide-acrylic acid resin (hydrolyzed polyacrylamide) is produced by the polymerization of acrylamide with partial hydrolysis, or by copolymerization of...

  19. 21 CFR 173.5 - Acrylate-acrylamide resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...prescribed conditions: (a) The additive consists of one of the following: (1) Acrylamide-acrylic acid resin (hydrolyzed polyacrylamide) is produced by the polymerization of acrylamide with partial hydrolysis, or by copolymerization of...

  20. 21 CFR 173.5 - Acrylate-acrylamide resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...prescribed conditions: (a) The additive consists of one of the following: (1) Acrylamide-acrylic acid resin (hydrolyzed polyacrylamide) is produced by the polymerization of acrylamide with partial hydrolysis, or by copolymerization of...

  1. 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.

  2. 21 CFR 177.1556 - Polyaryletherketone resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... water, 50 percent (by volume) ethyl alcohol in distilled water, 3 percent acetic acid (by weight) in... benzophenone and terephthaloyl dichloride in such a way that the finished resins have a minimum weight average molecular weight of 20,000 grams per mole, as determined by light scattering measurements in sulfuric...

  3. 21 CFR 177.1556 - Polyaryletherketone resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... water, 50 percent (by volume) ethyl alcohol in distilled water, 3 percent acetic acid (by weight) in... benzophenone and terephthaloyl dichloride in such a way that the finished resins have a minimum weight average molecular weight of 20,000 grams per mole, as determined by light scattering measurements in sulfuric...

  4. 21 CFR 177.1556 - Polyaryletherketone resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... water, 50 percent (by volume) ethyl alcohol in distilled water, 3 percent acetic acid (by weight) in... benzophenone and terephthaloyl dichloride in such a way that the finished resins have a minimum weight average molecular weight of 20,000 grams per mole, as determined by light scattering measurements in sulfuric...

  5. 21 CFR 177.1556 - Polyaryletherketone resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... water, 50 percent (by volume) ethyl alcohol in distilled water, 3 percent acetic acid (by weight) in... benzophenone and terephthaloyl dichloride in such a way that the finished resins have a minimum weight average molecular weight of 20,000 grams per mole, as determined by light scattering measurements in sulfuric...

  6. 21 CFR 177.1556 - Polyaryletherketone resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... temperature for 2 hours with the following solvents: Distilled water, 50 percent (by volume) ethyl alcohol in distilled water, 3 percent acetic acid (by weight) in distilled water, and n-heptane. (d) In testing the... such a way that the finished resins have a minimum weight average molecular weight of 20,000 grams...

  7. Separation of organic ion exchange resins from sludge -- engineering study

    SciTech Connect

    Duncan, J.B.

    1998-08-25

    This engineering study evaluates the use of physical separation technologies to separate organic ion exchange resin from KE Basin sludge prior to nitric acid dissolution. This separation is necessitate to prevent nitration of the organics in the acid dissolver. The technologies under consideration are: screening, sedimentation, elutriation. The recommended approach is to first screen the Sludge and resin 300 microns then subject the 300 microns plus material to elutriation.

  8. 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)

  9. 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.

  10. 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).

  11. Effect of pH and aging time on the kinetic dissociation of 243Am(III) from humic acid-coated gamma-Al2O3: a chelating resin exchange study.

    PubMed

    Wang, Xiangke; Chen, Changlun; Du, Jinzhou; Tan, Xiaoli; Di, Xu; Yu, Shaoming

    2005-09-15

    The chelating resin was studied to assess its influence on metal availability and mobility in the environment. The association of organic-inorganic colloid-borne trace elements was investigated in this work. The radionuclide 243Am(III) was chosen as the representative and chemical homologue for trivalent lanthanide and actinide ions present in radioactive nuclear waste. The kinetic dissociation behavior of 243Am(III) from humic acid-coated gamma-Al2O3 was studied at pH values of 4.0 +/- 0.1, 5.0 +/- 0.2, and 6.0 +/- 0.2 with a contact time of 2 days after the addition of a chelating cation exchanger resin. The concentrations of the components were: 243Am(III) 3.0 x 10(-7) mol/L, gamma-Al2O3 0.5 g/L, HA 10 mg/L (pH 4.0 +/- 0.1, 5.0 +/- 0.2, and 6.0 +/- 0.2) and 50 mg/L (pH 6.0 +/- 0.2), respectively. The kinetics of dissociation of 243Am(III) after different equilibration time with humic acid-coated gamma-Al2O3 was also investigated at pH 5.0 +/- 0.2. The experiments were carried out in air and at ambient temperature. The results suggest that the fraction of irreversible bonding of radionuclides to HA-coated Al2O3 increases with increasing pH and is independent of aging time. The assumption of two different 243Am(III)-HA-Al2O3 species, with "fast" and "slow" dissociation kinetics, is required to explain the experimental results. 243Am(III) species present on HA-Al2O3 colloids moves from the "fast" to the "slow" dissociating sites with the increase of aging time. PMID:16201632

  12. 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.

  13. 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 work to quantify mercury on sRF resin. Resin mercury content is important in plans for the disposition of used sRF resin. Mercury speciation in high level waste (HLW) is unknown. It may be partly organic, one example being methyl mercury cation. Further study of the resin's affinity for mercury is recommended.

  14. Adsorption of uranium ions by resins with amidoxime and amidoxime/carboxyl group prepared by radiation-induced polymerization

    NASA Astrophysics Data System (ADS)

    Choi, Seong-Ho; Choi, Min-Seok; Park, Yong-Tae; Lee, Kwang-Pill; Kang, Hee-Dong

    2003-06-01

    In order to recover uranium ions from seawater, chelate-type resins with amidoxime and amidoxime/carboxylic acid groups were prepared by radiation-induced polymerization of acrylonitrile (AN) and AN/acrylic acid and by subsequent amidoximation of cyano group of poly(AN), respectively. The resins were characterized by FT-IR, FT-Raman, solid-state 13C-NMR, SEM, and elemental analysis, respectively. The adsorption rate of uranium ion by resins with the amidoxime/carboxylic acid group were higher than that of resins with the amidoxime group. The adsorption of uranium ions in artificial seawater to chelate-type resins was also examined.

  15. 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.

  16. [Radiopacity of composite resins].

    PubMed

    Tamburús, J R

    1990-01-01

    The author studied the radiopacity of six composite resins, submitted to radiographic examination in standardized conditions, only with kilovoltage variations. Along with resins it was radiographed an aluminium penetrometer, to compare their optical densities. The results showed that kilovoltagem variations interfered in optical densities of the resins, being more pronounced in 50-55, 55-60 and 60-65 kilovoltages. Despite this, the relations of optical densities as compared with that of penetrometer steps kept unaltered most fo the kilovoltages used. PMID:2135338

  17. Applications of fossil resin studies to an understanding of depositional and paleoenvironments

    SciTech Connect

    Bellis, D.; Wolberg, D.L. )

    1989-09-01

    Fossil resins are polymerized terpene (isoprenoid) acids. Because of their complexity and resulting variability, isoprenoids have been useful for their information content and geochemical signatures. Fossil resin occurs throughout a 304-ft continuous core and correlated outcrops from the Late Cretaceous Fruitland Formation in the Fossil Forest study area, San Juan basin, New Mexico, in associated with coal, sandstone, shale, and petrified wood. Fourier transformation infrared (FTIR) spectra of resin from throughout the sequence reveal oxidative and chemical variation. FTIR spectra of resin incorporated in petrified wood differ from those of resin exposed to the paleoatmosphere in the same individual tree. This study was initiated to complement previous studies related to analyses of fluid inclusions in fossil resin and to elucidate reactions between the resin matrix and possible atmospheric inclusions. It was done in conjunction with extensive trace-element, palynological, and mineralogical analyses. Understanding the biogeochemistry of fossil resin may elucidate the origin, diagenesis, and depositional environment of smaller concentrations of isoprenoids.

  18. 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.

  19. Amino acid analysis

    NASA Technical Reports Server (NTRS)

    Winitz, M.; Graff, J. (inventors)

    1974-01-01

    The process and apparatus for qualitative and quantitative analysis of the amino acid content of a biological sample are presented. The sample is deposited on a cation exchange resin and then is washed with suitable solvents. The amino acids and various cations and organic material with a basic function remain on the resin. The resin is eluted with an acid eluant, and the eluate containing the amino acids is transferred to a reaction vessel where the eluant is removed. Final analysis of the purified acylated amino acid esters is accomplished by gas-liquid chromatographic techniques.

  20. 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.

  1. Two pentasaccharide resin glycosides from Argyreia acuta.

    PubMed

    Yin, Yong-Qin; Pan, Jie-Tao; Yu, Bang-Wei; Cui, Hong-Hua; Yan, You-Shao; Chen, Yan-Fen

    2016-01-01

    Two new compounds of acutacosides 1 and 2, pentasaccharide resin glycosides were isolated from the aerial parts of Argyreia acuta. The core of the two compounds was operculinic acid A, and they were esterfied at the same position, just one substituent group was linked at C-2 of Rha. The absolute configuration of the aglycone in the two compounds was established by Mosher's method, which was (11S)-hydroxyhexadecanoic acid (jalapinolic acid). Their structures were established by a combination of spectroscopic and chemical methods. PMID:25925631

  2. Alternate Methods For Eluting Cesium From Spherical Resorcinol-Formaldehyde Resin

    SciTech Connect

    Taylor, Paul Allen; Johnson, Heather Lauren

    2009-01-01

    A Small Column Ion Exchange (SCIX) system has been proposed for removing cesium from the supernate and dissolved salt solutions in the high level waste tanks at the Savannah River Site (SRS). The SCIX system could use either crystalline silicotitanate (CST) an inorganic, non-regenerable sorbent or spherical resorcinol-formaldehyde (RF), a new regenerable resin, to remove cesium from the waste solutions. The standard method for eluting the cesium from the RF resin uses 15-20 bed volumes (BV) of 0.5 M nitric acid (HNO3). The nitric acid eluate, containing the radioactive cesium, would be combined with the sludge from the waste tanks, and would be converted into glass at the Defense Waste Processing Facility (DWPF) at SRS. The amount of nitric acid generated by the standard elution method exceeds the capacity of DWPF to destroy the nitrate ions and maintain the required chemical reducing conditions in the glass melt. Alternate methods for eluting the resin have been tested, including using lower concentrations of nitric acid, other acids, and changing the flow regimes. About 4 bed volumes of 0.5 M nitric acid are required to remove the sodium (titrate the resin) and most of the cesium from the resin, so the bulk of the acid used for the standard elution method removes a very small quantity of cesium from the resin. The resin was loaded with 9.5 g Cs/L of resin prior to elution, which is the maximum expected loading for RF resin treating the actual dissolved salt waste at SRS. For the baseline elution method, 465 g of nitrate is used per liter of resin, and >99.9999% of the cesium is removed from the resin. An alternative method that used 4 bed volumes of 0.5 M HNO3 followed by 11 bed volumes of 0.05 M HNO3, used 158 g of nitrate per liter of resin (66% less nitrate than used for the standard elution) and removed >99.998% of the cesium. A staccato flow mode using 0.5 M HNO3 (1 hr on at 1 BV/hr, followed by 3 hrs off) after the resin had been titrated using a continuous flow of acid at 1 BV/hr removed 99.9998% of the cesium while using 12 BV of acid (20% less than the baseline). Formic acid was slightly less efficient than nitric acid for eluting the resin, but 20 BV of 0.5 M HCOOH removed 99.98% of the cesium from the resin.

  3. 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.

  4. 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.

  5. 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. (authors)

  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. 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.

  8. A NEW EXTRACTION CHROMATOGRAPHY RESIN CONTAINING KLÄUI LIGANDS FOR APPLICATION IN ACTINIDE SEPARATIONS

    SciTech Connect

    Lumetta, Gregg J.; Wester, Dennis W.; McNamara, Bruce K.; Hubler, Timothy L.; Latesky, Stanley L.; Martyr, Cuthbert C.; Richards, Kia N.

    2004-11-01

    An extraction chromatography resin containing the anionic ligand (?5-pentamethylcyclopentadienyl)tris-(diethylphosphito-P)cobalt(III), (L) has been prepared. The resin consists of 1 wt% L on Amberlite® XAD-7. This resin strongly sorbs Am(III) and Pu(IV). The sorption of these ions decreases with increasing nitric acid concentration, but this effect is more pronounced for Am(III). This allows for convenient separation of Am(III) from Pu(IV) by simple adjustments in the nitric acid concentration. The tripodal geometry of L disfavors the complexation of uranyl ion, so sorption of U(VI) by the L-containing resin is weak.

  9. Method for removing contaminants from plastic resin

    DOEpatents

    Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee's Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

    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.

  10. 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.

  11. Glycoprotein Enrichment Resin User Manual

    E-print Network

    Lebendiker, Mario

    Glycoprotein Enrichment Resin User Manual Cat. No. 635647 PT4050-1 (PR912675) Published 14 January Laboratories, Inc. Version No. PR912675 ATakara Bio Company 2 Glycoprotein Enrichment Resin User Manual I.................................................................................................4 IV. Glycoprotein Enrichment

  12. Flame Atomic Absorption Spectrometric Determination of Trace Metal Ions in Environmental and Biological Samples After Preconcentration on a Newly Developed Amberlite XAD-16 Chelating Resin Containing p-Aminobenzene Sulfonic Acid.

    PubMed

    Islam, Aminul; Ahmad, Akil; Laskar, Mohammad Asaduddin

    2015-01-01

    Amberlite® XAD-16 was functionalized with p-aminobenzene sulfonic acid via an azo spacer in order to prepare a new chelating resin, which was then characterized by water regain value, hydrogen ion capacity, elemental analyses, and IR spectral and thermal studies. The maximum uptake of Cu(II), Ni(II), Zn(II), Co(II), Cr(III), Fe(III), and Pb(II) ions was observed in the pH range 4.0-6.0 with the corresponding half-loading times of 6.5, 7.0, 8.0, 9.0, 11.0, 8.5, and 16.5 min. The sorption data followed Langmuir isotherms and a pseudo-second-order model. Thermodynamic quantities, ?H and ?S, based on the variation of the distribution coefficient with temperature were also evaluated. High preconcentration factors of 60-100 up to a low preconcentration limit of 4.0-6.6 ?g/L have been achieved for the metal ions. The validity of the method was checked by analyzing standard reference materials and recoveries of trace metals after spiking. The analytical applications of the method were explored by analyzing natural water, mango pulp, mint leaves, and fish. PMID:25857893

  13. Method for digesting spent ion exchange resins and recovering actinides therefrom using microwave radiation

    DOEpatents

    Maxwell, III, Sherrod L. (Aiken, SC); Nichols, Sheldon T. (Augusta, GA)

    1999-01-01

    The present invention relates to methods for digesting diphosphonic acid substituted cation exchange resins that have become loaded with actinides, rare earth metals, or heavy metals, in a way that allows for downstream chromatographic analysis of the adsorbed species without damage to or inadequate elution from the downstream chromatographic resins. The methods of the present invention involve contacting the loaded diphosphonic acid resin with concentrated oxidizing acid in a closed vessel, and irradiating this mixture with microwave radiation. This efficiently increases the temperature of the mixture to a level suitable for digestion of the resin without the use of dehydrating acids that can damage downstream analytical resins. In order to ensure more complete digestion, the irradiated mixture can be mixed with hydrogen peroxide or other oxidant, and reirradiated with microwave radiation.

  14. 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.

  15. Management of Spent Organic Ion-Exchange Resins by Photochemical Oxidation

    SciTech Connect

    Srinivas, C.; Sugilal, S.; Wattal, P. K.

    2003-02-26

    Management of spent ion-exchange resin waste arising from nuclear reactor operations by traditional practice of encapsulation in cement is associated with problems such as swelling and disintegration. Complete oxidation (mineralization) is an attractive alternative option. This paper reports the development of photochemical mineralization process for organic ion-exchange resins of poly (styrene-divinyl benzene) type with sulfonic acid and quaternary ammonium functional groups. It is a two-step process consisting of dissolution (conversion of solid resin into water-soluble reaction products) and photo-Fenton mineralization of the dissolved resin. Cation and anion resin dissolution was effected by reaction of the resin with H2O2 at 50-60 C in the presence of ferrous/copper sulphate catalyst. Direct dissolution of mixed resin was not efficient. However, the cation resin portion in the mixed resin could be selectively dissolved without affecting the anion portion. The solid anion resin after separation from the cation resin solution could be dissolved. About 0.5 liters of 50% H2O2 was required for dissolution of one kg of wet resin. The reaction time was 4-5 hours. Dissolution experiments were conducted on up to 8 liters of wet resin. The second step, viz., photo-Fenton mineralization of the dissolved resin was effected at ambient temperature(25-35 C). Kinetic results of laboratory scale experiments in immersion type photo-reactor and pilot scale experiments in tubular flow photo-reactor were presented. These results clearly demonstrated the photo-Fenton mineralization of dissolved resin at ambient temperature with stoichiometric quantity of H2O2 as against 70-200% excess H2O2 requirement in chemical mineralization experiments under Fenton oxidation conditions at 90-95 C. Based on these studies, a treatment scheme was developed and presented in this paper.

  16. Cementation of residue ion exchange resins at Rocky Flats

    SciTech Connect

    Dustin, D.F.; Beckman, T.D.; Madore, C.M.

    1998-03-03

    Ion exchange resins have been used to purify nitric acid solutions of plutonium at Rocky Flats since the 1950s. Spent ion exchange resins were retained for eventual recovery of residual plutonium, typically by incineration followed by the aqueous extraction of plutonium from the resultant ash. The elimination of incineration as a recovery process in the late 1980s and the absence of a suitable alternative process for plutonium recovery from resins led to a situation where spent ion exchange resins were simply placed into temporary storage. This report describes the method that Rocky Flats is currently using to stabilize residue ion exchange resins. The objective of the resin stabilization program is: (1) to ensure their safety during interim storage at the site, and (2) to prepare them for ultimate shipment to the Waste Isolation Pilot Plant (WIPP) in New Mexico. Included in the discussion is a description of the safety concerns associated with ion exchange resins, alternatives considered for their stabilization, the selection of the preferred treatment method, the means of implementing the preferred option, and the progress to date.

  17. 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.

  18. 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.

  19. Quantitative analysis of PMR-15 polyimide resin by HPLC

    NASA Technical Reports Server (NTRS)

    Roberts, Gary D.; Lauver, Richard W.

    1987-01-01

    The concentration of individual components and of total solids of 50 wt pct PMR-15 resin solutions was determined using reverse-phase HPLC to within + or - 8 percent accuracy. Acid impurities, the major source of impurities in 3,3', 4,4'-benzophenonetetracarboxylic acid (BTDE), were eliminated by recrystallizing the BTDE prior to esterification. Triester formation was not a problem because of the high rate of esterification of the anhydride relative to that of the carboxylic acid. Aging of PMR-15 resin solutions resulted in gradual formation of the mononadimide and bisnadimide of 4,4'-methylenedianiline, with the BTDE concentration remaining constant. Similar chemical reactions occurred at a reduced rate in dried films of PMR-15 resin.

  20. Removal of CdTe in acidic media by magnetic ion-exchange resin: a potential recycling methodology for cadmium telluride photovoltaic waste.

    PubMed

    Zhang, Teng; Dong, Zebin; Qu, Fei; Ding, Fazhu; Peng, Xingyu; Wang, Hongyan; Gu, Hongwei

    2014-08-30

    Sulfonated magnetic microspheres (PSt-DVB-SNa MPs) have been successfully prepared as adsorbents via an aqueous suspension polymerization of styrene-divinylbenzene and a sulfonation reaction successively. The resulting adsorbents were confirmed by means of Fourier transform infrared spectra (FT-IR), X-ray diffraction (XRD), transmission electron microscope (TEM), scanning electron microscope equipped with an energy dispersive spectrometer (SEM-EDS) and vibrating sample magnetometer (VSM). The leaching process of CdTe was optimized, and the removal efficiency of Cd and Te from the leaching solution was investigated. The adsorbents could directly remove all cations of Cd and Te from a highly acidic leaching solution of CdTe. The adsorption process for Cd and Te reached equilibrium in a few minutes and this process highly depended on the dosage of adsorbents and the affinity of sulfonate groups with cations. Because of its good adsorption capacity in strong acidic media, high adsorbing rate, and efficient magnetic separation from the solution, PSt-DVB-SNa MPs is expected to be an ideal material for the recycling of CdTe photovoltaic waste. PMID:25128764

  1. 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.

  2. Process for the preparation of lactic acid and glyceric acid

    DOEpatents

    Jackson, James E [Haslett, MI; Miller, Dennis J [Okemos, MI; Marincean, Simona [Dewitt, MI

    2008-12-02

    Hexose and pentose monosaccharides are degraded to lactic acid and glyceric acid in an aqueous solution in the presence of an excess of a strongly anionic exchange resin, such as AMBERLITE IRN78 and AMBERLITE IRA400. The glyceric acid and lactic acid can be separated from the aqueous solution. Lactic acid and glyceric acid are staple articles of commerce.

  3. Use of the 2-chlorotrityl chloride resin for microwave-assisted solid phase peptide synthesis.

    PubMed

    Ieronymaki, Matthaia; Androutsou, Maria Eleni; Pantelia, Anna; Friligou, Irene; Crisp, Molly; High, Kirsty; Penkman, Kirsty; Gatos, Dimitrios; Tselios, Theodore

    2015-09-01

    A fast and efficient microwave (MW)-assisted solid-phase peptide synthesis protocol using the 2-chlorotrityl chloride resin and the Fmoc/tBu methodology, has been developed. The established protocol combines the advantages of MW irradiation and the acid labile 2-chlorotrityl chloride resin. The effect of temperature during the MW irradiation, the degree of resin substitution during the coupling of the first amino acids and the rate of racemization for each amino acid were evaluated. The suggested solid phase methodology is applicable for orthogonal peptide synthesis and for the synthesis of cyclic peptides. PMID:26270247

  4. Environment and Genotype Affect Sweetpotato Storage Root Periderm Resin Glycoside Content

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Resin glycosides are complex compounds composed primarily of fatty acids and sugars that contribute to allelopathic potential and pest resistance in sweetpotato. Total periderm resin glycoside (PRG) contents of 10 sweetpotato (Ipomoea batatas L.) clones grown in three different field trials was det...

  5. 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.

  6. System for removing contaminants from plastic resin

    DOEpatents

    Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee's Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

    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.

  7. 40 CFR Table 2 to Subpart Ooo of... - Known Organic Hazardous Air Pollutants (HAP) From the Manufacture of Amino/Phenolic Resins

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...HAP) From the Manufacture of Amino/Phenolic Resins 2 Table...Pollutant Emissions: Manufacture of Amino/Phenolic Resins Pt. 63...HAP) From the Manufacture of Amino/Phenolic Resins Organic... Yes Cresol and cresylic acid (mixed) 1319-77-3...

  8. 40 CFR Table 2 to Subpart Ooo of... - Known Organic Hazardous Air Pollutants (HAP) From the Manufacture of Amino/Phenolic Resins

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...HAP) From the Manufacture of Amino/Phenolic Resins 2 Table...Pollutant Emissions: Manufacture of Amino/Phenolic Resins Pt. 63...HAP) From the Manufacture of Amino/Phenolic Resins Organic... Yes Cresol and cresylic acid (mixed) 1319-77-3...

  9. 40 CFR Table 2 to Subpart Ooo of... - Known Organic Hazardous Air Pollutants (HAP) From the Manufacture of Amino/Phenolic Resins

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...HAP) From the Manufacture of Amino/Phenolic Resins 2 Table...Pollutant Emissions: Manufacture of Amino/Phenolic Resins Pt. 63...HAP) From the Manufacture of Amino/Phenolic Resins Organic... Yes Cresol and cresylic acid (mixed) 1319-77-3...

  10. 40 CFR Table 2 to Subpart Ooo of... - Known Organic Hazardous Air Pollutants (HAP) From the Manufacture of Amino/Phenolic Resins

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...HAP) From the Manufacture of Amino/Phenolic Resins 2 Table...Pollutant Emissions: Manufacture of Amino/Phenolic Resins Pt. 63...HAP) From the Manufacture of Amino/Phenolic Resins Organic... Yes Cresol and cresylic acid (mixed) 1319-77-3...

  11. 40 CFR Table 2 to Subpart Ooo of... - Known Organic Hazardous Air Pollutants (HAP) From the Manufacture of Amino/Phenolic Resins

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...HAP) From the Manufacture of Amino/Phenolic Resins 2 Table...Pollutant Emissions: Manufacture of Amino/Phenolic Resins Pt. 63...HAP) From the Manufacture of Amino/Phenolic Resins Organic... Yes Cresol and cresylic acid (mixed) 1319-77-3...

  12. Retrofit for Plastic Resin Driers 

    E-print Network

    Joseph, B.; Thuro, G.

    1991-01-01

    RESIN DRIERS BABU JOSEPH PH.D. Supervising Engineer Southern California Edison Company, Irwindale, California GEORGE THURO Thuro, & Associates, Costa Mesa, California Plastic resins used in injection molding have to be dried to specified..., and vary depending on the resin, the mold and the molding process. Typically the drier is set for the worst possible conditions. So there are opportunities for energy savings. This study conducted by Southern California Edison Company has identified...

  13. Vitrification of ion exchange resins

    DOEpatents

    Cicero-Herman, Connie A. (Aiken, SC); Workman, Rhonda Jackson (North Augusta, SC)

    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.

  14. 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

  15. 21 CFR 872.3140 - Resin applicator.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... DEVICES DENTAL DEVICES Prosthetic Devices § 872.3140 Resin applicator. (a) Identification. A resin applicator is a brushlike device intended for use in spreading dental resin on a tooth during application...

  16. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 3 2013-04-01 2013-04-01 false Terpene resins. 178.3930 Section 178.3930 Food...Certain Adjuvants and Production Aids § 178.3930 Terpene resins. The terpene resins identified in paragraph (a) of...

  17. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 3 2012-04-01 2012-04-01 false Terpene resins. 178.3930 Section 178.3930 Food...Certain Adjuvants and Production Aids § 178.3930 Terpene resins. The terpene resins identified in paragraph (a) of...

  18. Uptake of actinides and other ions by Diphosil, a new silica-based chelating ion exchange resin

    SciTech Connect

    Chiarizia, R.; Horwitz, E.P.; D`Arcy, K.A.; Alexandratos, S.D.; Trochimczuk

    1996-06-01

    After adsorption of actinides on a phosphonic acid resin, it may be desirable to leave the actinides on the resin. It may be preferable that the polymeric resin matrix be replaced by an inorganic material, in order to prevent formation of radiolytic gases from the organic polymer. A new version of the Diphonix resin has been prepared, where the chelating diphosphonic acid groups are grafted to a silica support. This material is called Diphosil, for Diphonix on silica. This paper reports some results on equilibrium and kinetics of uptake of a number of actinide species and other metal ions of nuclear, environmental, or hydrometallurgical interest by Diphosil.

  19. Investigating the Use of Ion Exchange Resins for Processing Biodiesel Feedstocks 

    E-print Network

    Jamal, Yousuf 1973-

    2012-11-27

    feedstocks. Specifically, this research explored using ion exchange resins to remove free fatty acids (FFA) from soybean and waste cooking oils, catalyze transesterification of soybean oil, and catalyze in-situ conversion of dried algal biomass to biodiesel...

  20. 21 CFR 175.320 - Resinous and polymeric coatings for polyolefin films.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...copolymer Terpene resins consisting of polymers of ?-pinene, ?-pinene, and/or dipentene; acid value less than 5, saponification number less than 5, and color less than 4 on the Gardner scale as measured in 50 percent mineral spirits solution...

  1. 40 CFR Appendix B to Subpart Nnn... - Free Formaldehyde Analysis of Insulation Resins by Hydroxylamine Hydrochloride

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...other phenolic resins, especially those with a high FF content. 2. Principle 2.1a. The basis for this method is the titration of the hydrochloric acid that is liberated when hydroxylamine hydrochloride reacts with formaldehyde to form...

  2. 40 CFR Appendix B to Subpart Nnn... - Free Formaldehyde Analysis of Insulation Resins by Hydroxylamine Hydrochloride

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...other phenolic resins, especially those with a high FF content. 2. Principle 2.1a. The basis for this method is the titration of the hydrochloric acid that is liberated when hydroxylamine hydrochloride reacts with formaldehyde to form...

  3. 40 CFR Appendix B to Subpart Nnn... - Free Formaldehyde Analysis of Insulation Resins by Hydroxylamine Hydrochloride

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...other phenolic resins, especially those with a high FF content. 2. Principle 2.1a. The basis for this method is the titration of the hydrochloric acid that is liberated when hydroxylamine hydrochloride reacts with formaldehyde to form...

  4. 40 CFR Appendix B to Subpart Nnn... - Free Formaldehyde Analysis of Insulation Resins by Hydroxylamine Hydrochloride

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...other phenolic resins, especially those with a high FF content. 2. Principle 2.1a. The basis for this method is the titration of the hydrochloric acid that is liberated when hydroxylamine hydrochloride reacts with formaldehyde to form...

  5. 40 CFR Appendix B to Subpart Nnn... - Free Formaldehyde Analysis of Insulation Resins by Hydroxylamine Hydrochloride

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...other phenolic resins, especially those with a high FF content. 2. Principle 2.1a. The basis for this method is the titration of the hydrochloric acid that is liberated when hydroxylamine hydrochloride reacts with formaldehyde to form...

  6. Furfural resin-based bio-nanocomposites reinforced by reactive nanocrystalline cellulose

    NASA Astrophysics Data System (ADS)

    Wang, C.; Sun, S.; Zhao, G.; He, B.; Xiao, H.

    2009-07-01

    The work presented herein has been focused on reinforcing the furfural resins (FA) by reactive-modified nanocrystalline cellulose (NCC) in an attempt to create a bio-nanocomposite completely based on natural resources. FA prepolymers were synthesized with an acid catalyst, and NCC was rendered reactive via the grafting of maleic anhydride (MAH). The resulting NCC and nanocomposites were characterized using TEM, SEM and FT-IR. It was found that NCC appeared to be spherical in shape with diameters under 100 nm. FT-IR confirmed that there were hydrogen and esterification bonding between MAH and NCC or FA prepolymer. After solidified with paratoluenesulfonic acid, NCC-reinforced FA resin composites showed granular cross-section while FA resin with layered structures. Mechanical property tests indicated that NCC-reinforced FA resin composites possessed the improved tensile and flexural strengths, in comparison with FA resin.

  7. WEAK-ACID ION EXCHANGE FOR REMOVING BARIUM, RADIUM, AND HARDNESS

    EPA Science Inventory

    Weak-acid resin in the hydrogen form was found to effectively remove barium, radium, and hardness, without increasing the sodium content of the product water. The maximum capacity of the weak-acid resin was about 2.3 times that of strong-acid resin, and much less spent regenerant...

  8. Eichrom`s Diphonix{reg_sign} resin: Production-scale applications in radioactive waste treatment and iron control in copper electrowinning

    SciTech Connect

    Gula, M.J.; Chang, F.; Dreisinger, D.B.; Horwitz, E.P.

    1997-12-31

    Eichrom`s Diphonix{reg_sign} resin has been phased through synthetic scale-up, pilot testing, and production installation in radioactive waste treatment and hydrometallurgical applications. The geminal diphosphonic acid groups of Diphonix resin allow selective retention by cation-exchange and/or chelation. The resin is effective at low pH where sulfonic and carboxylic acid resins are ineffective. Diphonix resin has been used in nuclear facilities to reduce actinide concentrations in radioactive waste effluents and to reduce waste volumes. The high retention of iron(III) by Diphonix resin in acidic sulfate media has led to an installation capable of removing one ton of iron per day from a copper electrowinning stream. This iron control process diminishes cobalt losses in the electrowinning circuit and significantly reduces operating costs. The authors will discuss the development of these Diphonix resin applications.

  9. 21 CFR 175.300 - Resinous and polymeric coatings.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    .... Rosins listed in paragraph (b)(3)(v)(a) of this section, for use only as reactants in oil-based or fatty acid-based alkyd resins. (c) Polyhydric alcohols: Butylene glycol. Diethylene glycol. 2,2-Dimethyl-1,3... chemically treated with one or more of the following substances: Allyl ether of mono-, di-,...

  10. 21 CFR 175.300 - Resinous and polymeric coatings.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...)(v)(a) of this section, for use only as reactants in oil-based or fatty acid-based alkyd resins. (c... chemically treated with one or more of the following substances: Allyl ether of mono-, di-, or... more of the following substances: Allyl ether of mono-, di-, or trimethylol phenol....

  11. 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

  12. An Engineering Evaluation of Spherical Resorcinol Formaldehyde Resin

    SciTech Connect

    Birdwell Jr, Joseph F; Lee, Denise L; Taylor, Paul Allen; Collins, Robert T; Hunt, Rodney Dale

    2010-09-01

    A small column ion exchange (SCIX) system has been proposed for removal of cesium from caustic, supernatant, and dissolved salt solutions stored or generated from high-level tank wastes at the US Department of Energy (DOE) Hanford Site and Savannah River Sites. In both instances, deployment of SCIX systems, either in-tank or near-tank, is a means of expediting waste pretreatment and dispositioning with minimal or no new infrastructure requirements. Conceptually, the treatment approach can utilize a range of ion exchange media. Previously, both crystalline silicotitanate (CST), an inorganic, nonelutable sorbent, and resorcinol-formaldehyde (RF), an organic, elutable resin, have been considered for cesium removal from tank waste. More recently, Pacific Northwest National Laboratory (PNNL) evaluated use of SuperLig{reg_sign} 644, an elutable ion exchange medium, for the subject application. Results of testing indicate hydraulic limitations of the SuperLig{reg_sign} resin, specifically a high pressure drop through packed ion exchange columns. This limitation is likely the result of swelling and shrinkage of the irregularly shaped (granular) resin during repeated conversions between sodium and hydrogen forms as the resin is first loaded then eluted. It is anticipated that a similar flow limitation would exist in columns packed with conventional, granular RF resin. However, use of spherical RF resin is a likely means of mitigating processing limitations due to excessive pressure drop. Although size changes occur as the spherical resin is cycled through loading and elution operations, the geometry of the resin is expected to effectively mitigate the close packing that leads to high pressure drops across ion exchange columns. Multiple evaluations have been performed to determine the feasibility of using spherical RF resin and to obtain data necessary for design of an SCIX process. The work performed consisted of examination of radiation effects on resin performance, quantification of cesium adsorption performance as a function of operating temperature and pH, and evaluation of sodium uptake (titration) as function of pH and counteranion concentration. The results of these efforts are presented in this report. Hydraulic performance of the resin and the use of eluant alternatives to nitric acid have also been evaluated and have been reported elsewhere (Taylor 2009, Taylor and Johnson 2009).

  13. 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.

  14. 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 (?-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 ?-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 ?-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 ?-SBS of the Wave group and the Margin Bond group. However, the ?-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 resins to enamel and porcelain substrates. PMID:25540657

  15. 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 ?m 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

  16. 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, 3,4'-oxydianiline (3,4'-ODA), 1,3-bis(3-aminophenoxy) benzene (1,3-APB), and 4-phenylethynylphthalic anhydride (PEPA). PERA-1 was made from 3,5-diamino- 4.-phenylethynylbenzophenon and equimolar amounts of phthalic anhydride and PEPA. To make PERA-1 in the imide form, the aforementioned ingredients were processed by refluxing in glacial acetic acid. To make the amide form of PERA-1, the ingredients were reacted in N-methyl-2-pyrrolidinone (NMP) under nitrogen at a temperature of 23 C (see figure). On the basis of the processability and other properties, a blend comprising 20 weight percent of PERA-1 and 80 weight percent PETI-5 was selected for further evaluation. Relative to neat PETI-5, the blend exhibited an increase in Tg; improved processability; and comparable values of shear strength in adhesion to titanium panels, open-hole compressive properties, compression properties after impact, and resistance to microcracking.

  17. Effects of 'resin-compatible' cavity varnishes on composite resin microhardness.

    PubMed

    Chan, K C; Swift, E J

    1992-06-01

    Although the use of cavity varnishes with composite resins has traditionally been discouraged, several "resin-compatible" varnishes are currently available. This in vitro study evaluated the effects of resin-compatible cavity varnishes on a hybrid composite resin. The results of the study indicate that these varnishes soften the composite resin in contact with varnished dentin. PMID:1403861

  18. Chromatography resin support

    DOEpatents

    Dobos, James G. (North Augusta, SC)

    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.

  19. 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.

  20. 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.

  1. Grafted methylenediphosphonate ion exchange resins

    DOEpatents

    Trochimcznk, Andrzej W. (Knoxbille, TN); Gatrone, Ralph C. (Plymouth, PA); Alexandratos, Spiro (Knoxville, TN); Horwitz, E. Philip (Naperville, IL)

    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.

  2. Grafted methylenediphosphonate ion exchange resins

    DOEpatents

    Trochimcznk, Andrzej W. (Knoxville, TN); Gatrone, Ralph C. (Plymouth, PA); Alexandratos, Spiro (Knoxville, TN); Horwitz, E. Philip (Naperville, IL)

    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.

  3. 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.

  4. Alkyd-amino resins based on waste PET for coating applications

    SciTech Connect

    Torlakoglu, A.; Gueclue, G.

    2009-01-15

    Waste polyethylene terephthalate (PET) flakes were depolymerized by using propylene glycol (PG) in the presence of zinc acetate as catalyst. Glycolysis reaction products of waste PET obtained by using PET/glycol molar ratio 1/2. Two short oil alkyd resins of high acid values (30-40 mgKOH/g) were prepared from phthalic anhydride (PA), glycerin (G), coconut oil fatty acids (COFA) and glycolyzed products of waste PET (PET-based alkyd resins) or glycols (PG) (reference alkyd resins). These alkyd resins were blended with 30%, 40%, and 50% of a commercial urea-formaldehyde, melamine-formaldehyde and urea-formaldehyde/melamine-formaldehyde mixture (1/1 weight ratio) and heated at 140 deg. C. The physical and chemical properties such as drying time, hardness, abrasion resistance, adhesion strength, water resistance, alkaline resistance, acid resistance, gelation time, and thermal oxidative degradation resistance (with thermogravimetric analysis, TGA) of these alkyd-amino resins were investigated. The properties of the waste PET-based resins were found to be compatible with the properties of the reference resins.

  5. Technical Task and Quality Assurance Plan in Support of BNFL Part B: Studies of Ion Exchange Resin Integrity under Flowsheet Extremes: Part II

    SciTech Connect

    Nash, C.A.

    2000-08-23

    This task will address four items related to ion exchange stability: (1) process upset evaluation of resin in contact with 1 molar sodium permanganate at 25 and 40 degrees C, (2) accelerated aging with nitric acid solution used during normal regeneration operations, (3) prolonged contacting of SuperLig 644 resin with 5 molar nitric acid at room temperature, and (4) prolonged contacting of SuperLig 644 resin with deionized water at 60 plus/minus 5 degrees C.

  6. Methane production using resin-wafer electrodeionization

    SciTech Connect

    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.

  7. Cariogenic bacteria degrade dental resin composites and adhesives.

    PubMed

    Bourbia, M; Ma, D; Cvitkovitch, D G; Santerre, J P; Finer, Y

    2013-11-01

    A major reason for dental resin composite restoration replacement is related to secondary caries promoted by acid production from bacteria including Streptococcus mutans (S. mutans). We hypothesized that S. mutans has esterase activities that degrade dental resin composites and adhesives. Standardized specimens of resin composite (Z250), total-etch (Scotchbond Multipurpose, SB), and self-etch (Easybond, EB) adhesives were incubated with S. mutans UA159 or uninoculated culture medium (control) for up to 30 days. Quantification of the BisGMA-derived biodegradation by-product, bishydroxy-propoxy-phenyl-propane (BisHPPP), was performed by high-performance liquid chromatography. Surface analysis of the specimens was performed by scanning electron microscopy (SEM). S. mutans was shown to have esterase activities in levels comparable with those found in human saliva. A trend of increasing BisHPPP release throughout the incubation period was observed for all materials and was more elevated in the presence of bacteria vs. control medium for EB and Z250, but not for SB (p < .05). SEM confirmed the increased degradation of all materials with S. mutans UA159 vs. control. S. mutans has esterase activities at levels that degrade resin composites and adhesives; degree of degradation was dependent on the material's chemical formulation. This finding suggests that the resin-dentin interface could be compromised by oral bacteria that contribute to the progression of secondary caries. PMID:24026951

  8. Epoxy hydantoins as matrix resins

    NASA Technical Reports Server (NTRS)

    Weiss, J.

    1983-01-01

    Tensile strength and fracture toughness of castings of the hydantoin resins cured with methylenedianiline are significantly higher than MY 720 control castings. Water absorption of an ethyl, amyl hydantoin formulation is 2.1 percent at equilibrium and Tg's are about 160 C, approximately 15 deg below the final cure temperature. Two series of urethane and ester-extended hydantoin epoxy resins were synthesized to determine the effect of crosslink density and functional groups on properties. Castings cured with methylenedianiline or with hexahydrophthalic anhydride were made from these compounds and evaluated. The glass transition temperatures, tensile strengths and moduli, and fracture toughness values were all much lower than that of the simple hydantoin epoxy resins. Using a methylene bishydantoin epoxy with a more rigid structure gave brittle, low-energy fractures, while a more flexible, ethoxy-extended hydantoin epoxy resin gave a very low Tg.

  9. Phenolic cation-exchange resin material for recovery of cesium and strontium. [Patent application

    DOEpatents

    Ebra, M.A.; Wallace, R.M.

    1982-05-05

    A phenolic cation exchange resin with a chelating group has been prepared by reacting resorcinol with iminodiacetic acid in the presence of formaldehyde at a molar ratio of about 1:1:6. The material is highly selective for the simultaneous recovery of both cesium and strontium from aqueous alkaline solutions, such as, aqueous alkaline nuclear wate solutions. The organic resins are condensation polymers of resorcinol and formaldehyde with attached chelating groups. The column performance of the resins compares favorably with that of commercially available resins for either cesium or strontium removal. By combining Cs/sup +/ and Sr/sup 2 +/ removal in the same bed, the resins allow significant reduction of the size and complexity of facilities for processing nuclear waste.

  10. Phenolic cation exchange resin material for recovery of cesium and strontium

    DOEpatents

    Ebra, Martha A. (Aiken, SC); Wallace, Richard M. (Aiken, SC)

    1983-01-01

    A phenolic cation exchange resin with a chelating group has been prepared by reacting resorcinol with iminodiacetic acid in the presence of formaldehyde at a molar ratio of about 1:1:6. The material is highly selective for the simultaneous recovery of both cesium and strontium from aqueous alkaline solutions, such as, aqueous alkaline nuclear waste solutions. The organic resins are condensation polymers of resorcinol and formaldehyde with attached chelating groups. The column performance of the resins compares favorably with that of commercially available resins for either cesium or strontium removal. By combining Cs.sup.+ and Sr.sup.2+ removal in the same bed, the resins allow significant reduction of the size and complexity of facilities for processing nuclear waste.

  11. K Basin sludge/resin bead separation test report

    SciTech Connect

    Squier, D.M.

    1998-08-25

    The K Basin 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 minor amounts of other organic material. The sludge will be collected and treated for storage and eventual disposal. This process will remove the large solid materials by a 1/4 inch screen. The screened material will be subjected to nitric acid in a chemical treatment process. The organic ion exchange resin beads produce undesirable chemical reactions with the nitric acid. The resin beads must be removed from the bulk material and treated by another process. An effective bead separation method must extract 95% of the resin bead mass without entraining more than 5% of the other sludge component mass. The test plan I-INF-2729, ``Organic Ion Exchange Resin Separation Methods Evaluation,`` proposed the evaluation of air lift, hydro cyclone, agitated slurry and elutriation resin bead separation methods. This follows the testing strategy outlined in section 4.1 of BNF-2574, ``Testing Strategy to Support the Development of K Basins Sludge Treatment Process``. Engineering study BNF-3128, ``Separation of Organic Ion Exchange Resins from Sludge,`` Rev. 0, focused the evaluation tests on a method that removed the fine sludge particles by a sieve and then extracted the beads by means of a elutriation column. Ninety-nine percent of the resin beads are larger than 125 microns and 98.5 percent are 300 microns and larger. Particles smaller than 125 microns make up the largest portion of sludge in the K Basins. Eliminating a large part of the sludge`s non-bead component will reduce the quantity that is lifted with the resin beads in the elutriation column. Resin bead particle size distribution measurements are given in Appendix A The Engineering Testing Laboratory conducted measurements of a elutriation column`s ability to extract resin beads from a sieved, non-radioactive sludge simulant. A elutriation column uses a constant velocity upward flow stream to segregate materials. In simplistic terms, the dense particles fall to the column`s bottom while the flow lifts less dense particles to the column`s top. A particle can be streamlined or have a high drag profile; this factor also influences the lift or fall of a particle exposed to the column flow. The sludge components that lift or fall are determined by the fluid velocity. The column flow velocity needed to lift the bulk of the resin beads will also lift other, non-bead, sludge components. Resin bead treatment and disposal are complicated by large quantities of non-bead material. Tests are necessary to determine a column flow velocity that will collect the bulk of the resin beads and the amount of non-bead sludge components that are also collected.

  12. 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.

  13. Coemulsion and electrodeposition properties of mixtures of cationic epoxy resin and cationic acrylic resin containing butoxymethylamide groups

    SciTech Connect

    Chinping Yang; Yahnhaur Chen . Dept. of Chemical Engineering)

    1993-10-15

    Butyl acrylate, styrene, N,N-dimethylaminoethylmethacrylate, and N-(n-butoxy-methyl) acrylamide were copolymerized to prepare a cationic acrylic copolymer (I) containing butoxymethylamide groups. This copolymer can be mixed with an epoxy-amine adduct (II), acetic acid, and deionized water to form a coemulsion containing two cationic resins. The electrophoretic codeposition of the coemulsion and physical and chemical properties of the deposited film were investigated. The resin composition of film deposited from coemulsion was determined by Fourier transform Infrared (FTIR) quantitative analysis to study the coemulsion and electrophoretic codeposition behavior. The applicability of this two-component coemulsion in primer-surfacer (pricer) electrodeposition paint was also discussed. The results indicate that at any coemulsion resin composition the resin composition of electrodeposited film is almost equal to the coemulsion resin composition. The throwing power of emulsion increases with increasing applied voltage, as expected. However, the throwing power of coemulsion is almost equal to that of the II emulsion but greater than that of the I emulsion. Furthermore, all cured films derived from mixtures of I/II show excellent adhesive strength, good hardness, and high levels of salt spray resistance.

  14. Fatigue of the Resin-Enamel Bonded Interface and the Mechanisms of Failure

    PubMed Central

    Yahyazadehfar, Mobin; Mutluay, Mustafa Murat; Majd, Hessam; Ryou, Heonjune; Arola, Dwayne

    2013-01-01

    The durability of adhesive bonds to enamel and dentin and the mechanisms of degradation caused by cyclic loading are important to the survival of composite restorations. In this study a novel method of evaluation was used to determine the strength of resin-enamel bonded interfaces under both static and cyclic loading, and to identify the mechanisms of failure. Specimens with twin interfaces of enamel bonded to commercial resin composite were loaded in monotonic and cyclic 4-point flexure to failure within a hydrated environment. Results for the resin-enamel interface were compared with those for the resin composite (control) and values reported for resin-dentin adhesive bonds. Under both modes of loading the strength of the resin-enamel interface was significantly (p?0.0001) lower than that of the resin composite and the resin-dentin bonded interface. Fatigue failure of the interface occurred predominately by fracture of enamel, adjacent to the interface, and not due to adhesive failures. In the absence of water aging or acid production of biofilms, the durability of adhesive bonds to enamel is lower than that achieved in dentin bonding. PMID:23571321

  15. Modeling Ion-Exchange Processing With Spherical Resins For Cesium Removal

    SciTech Connect

    Hang, T.; Nash, C. A.; Aleman, S. E.

    2012-09-19

    The spherical Resorcinol-Formaldehyde and hypothetical spherical SuperLig(r) 644 ion-exchange resins are evaluated for cesium removal from radioactive waste solutions. Modeling results show that spherical SuperLig(r) 644 reduces column cycling by 50% for high-potassium solutions. Spherical Resorcinol Formaldehyde performs equally well for the lowest-potassium wastes. Less cycling reduces nitric acid usage during resin elution and sodium addition during resin regeneration, therefore, significantly decreasing life-cycle operational costs. A model assessment of the mechanism behind ''cesium bleed'' is also conducted. When a resin bed is eluted, a relatively small amount of cesium remains within resin particles. Cesium can bleed into otherwise decontaminated product in the next loading cycle. The bleed mechanism is shown to be fully isotherm-controlled vs. mass transfer controlled. Knowledge of residual post-elution cesium level and resin isotherm can be utilized to predict rate of cesium bleed in a mostly non-loaded column. Overall, 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. This evaluation justifies further development of a spherical form of the SL644 resin.

  16. The adsorption of lead and copper from aqueous solution on modified peat-resin particles.

    PubMed

    Sun, Q Y; Lu, P; Yang, L Z

    2004-01-01

    Raw peat was modified with sulfuric acid, then mixed modified with resin to prepare the modified peat-resin particles. Using the batch experimental systems, the removal of heavy metals (copper and lead) on the modified peat-resin particles was investigated. The data of the adsorption isotherm could be fitted by the Langmuir equation well. The adsorption rate of heavy metals on modified peat-resin particles was very swift. The removal processes of heavy metals on modified peat-resin particles could be well described by pseudo-second order model. The adsorption rate of lead was affected by the initial heavy metal concentration, initial pH, particle size, agitation speed and particle mass. In the adsorption of heavy metals (lead and copper) on the modified peat-resin particles, ion exchange was the major reaction mechanism. Desorption data showed that the lead adsorbed by modified peat-resin particle could be desorbed by 0.5 N or 1.0 N HNO3. The desorption rate was swift. The experiments indicated that the modified peat-resin particles have great potential for the removal of heavy metals from wastewater. PMID:15499788

  17. Bond strength of self-adhesive resin cements to composite submitted to different surface pretreatments

    PubMed Central

    dos Santos, Victor Hugo; Griza, Sandro; de Moraes, Rafael Ratto

    2014-01-01

    Objectives Extensively destroyed teeth are commonly restored with composite resin before cavity preparation for indirect restorations. The longevity of the restoration can be related to the proper bonding of the resin cement to the composite. This study aimed to evaluate the microshear bond strength of two self-adhesive resin cements to composite resin. Materials and Methods Composite discs were subject to one of six different surface pretreatments: none (control), 35% phosphoric acid etching for 30 seconds (PA), application of silane (silane), PA + silane, PA + adhesive, or PA + silane + adhesive (n = 6). A silicone mold containing a cylindrical orifice (1 mm2 diameter) was placed over the composite resin. RelyX Unicem (3M ESPE) or BisCem (Bisco Inc.) self-adhesive resin cement was inserted into the orifices and light-cured. Self-adhesive cement cylinders were submitted to shear loading. Data were analyzed by two-way ANOVA and Tukey's test (p < 0.05). Results Independent of the cement used, the PA + Silane + Adhesive group showed higher microshear bond strength than those of the PA and PA + Silane groups. There was no difference among the other treatments. Unicem presented higher bond strength than BisCem for all experimental conditions. Conclusions Pretreatments of the composite resin surface might have an effect on the bond strength of self-adhesive resin cements to this substrate. PMID:24516824

  18. Effect of solution concentration and aging conditions on PMR-15 resin

    NASA Technical Reports Server (NTRS)

    Roberts, G. D.; Vannucci, R. D.

    1986-01-01

    High performance liquid chromatography is utilized to evaluate the effect of temperature, solution concentration, and aging time on PMR-15 resin solutions. Fifty- and 70-wt percent PMR-15 resin solutions were prepared from the mixture of 5-norbornene-2,3-dicarboxylic ester (NE) acid, 4.4'-methylenedianiline (MDA), methanol, and 3,3',4.4.-benzophenonetetracarboxylic dimethyl ester (BTDE) acid solution. It is observed that in PMR-15 resin solution aged for 35 days at room temperature NE and MDA react to form amide and imide intermediates. The precipitation data reveal that in the 70-wt percent solution precipitation occurs after 12 days and in the 50-wt percent solution after 20 days; however, at lower temperatures (-11 C, and 2 C) no precipitation is detected. It is concluded that storage of resin solutions and powders at reduced temperatures extends shelf life by reducing the rate of imide formation.

  19. Solvent impregnated resin for isolation of U(VI) from industrial wastes

    SciTech Connect

    Karve, M.; Rajgor, R.V.

    2008-07-01

    A solid-phase extraction method based upon impregnation of Cyanex 302 (bis(2,4,4- trimethylpentyl)mono-thio-phosphinic acid) on Amberlite XAD-2 resin is proposed for isolation of U(VI) from uranmicrolite ore tailing samples and industrial effluent samples. U(VI) was sorbed from nitric acid media on the solvent-impregnated resin (SIR) and was recovered completely with 1.0 M HCl. Based upon sorption behavior of U(VI) with Cyanex 302, it was quantitatively sorbed on the SIR in a dynamic method, while the other metal ions were not sorbed by the modified resin. The preparation of impregnated resin is simple, based upon physical interaction of the extractant and solid support, has good sorption capacity for U(VI), and is also reliable for detection of traces of U(VI). (authors)

  20. Distribution Coefficients (Kd Values) for Waste Resins Generated from the K and L Disassembly Basin Facilities

    SciTech Connect

    Kaplan, D.I.

    2002-12-02

    The objective of this study was to measure 14C, 129I, and 99Tc Kd values of spent resin generated from the K and L Disassembly Basin Facilities. The scope of the work was to conduct Kd measurements of resins combined in the ratio that they are disposed, 42:58 cation:anion. Because it was not known how these spent resins would be buried, it was necessary to measure the Kd values in such a manner as to simulate both trench and vault disposal. This was accomplished by using an acid-rain simulant (a standard U.S. Environmental Protection Agency protocol) and a cement leachate simulant .

  1. 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.

  2. Improved and selective platinum recovery from spent alpha-alumina supported catalysts using pretreated anionic ion exchange resin.

    PubMed

    Shams, K; Goodarzi, F

    2006-04-17

    Improved and selective recovery of platinum from a spent dehydrogenation platinum alpha-alumina supported catalyst using a strong basic ion exchange resin is reported. Platinum and other precious metal group (PMG) complexes are leached using concentrated hydrochloric acid along with about 0.20 vol.% nitric acid as an oxidizing agent from de-coked and crushed spent catalyst. Effects of hydrochloric acid concentration, time, and temperature in leaching stage are investigated. The strong basic anionic resin is treated by sodium hydroxide solution to replace chloride anion by hydroxyl group ion. The supernatant of the leaching process is passed through a fixed column of hydroxylated strong base anionic resin. The treated resin on which the platinum complex is adsorbed is dried and burned in an oxidizing atmosphere at 750-800 degrees C. The recovered gray metallic powder is mainly platinum. Results compared with those obtained from untreated anionic resin show that adsorption of platinum complexes onto the treated anionic resin is more selective and the yield of separation is considerably improved. The breakthrough curves of the pretreated anion exchanger and that of untreated exchange resin reveals that the capacity of the hyroxilated resin is decreased by about 14%. These breakthrough curves can be used for calculation of height of a practical exchange plate (HPEP) for design purposes. PMID:16260084

  3. Alternate Methods for Eluting Cesium from Spherical Resorcinol-Formaldehyde Resin

    SciTech Connect

    Taylor, Paul Allen; Johnson, Heather Lauren

    2009-02-01

    A small-column ion exchange (SCIX) system has been proposed for removing cesium from the supernate and dissolved salt solutions in the high-level-waste tanks at the Savannah River Site (SRS). The SCIX system could use either crystalline silicotitanate (CST), an inorganic, non-regenerable sorbent, or spherical resorcinol-formaldehyde (RF), a new regenerable resin, to remove cesium from the waste solutions. The baseline method for eluting the cesium from the RF resin uses 15 bed volumes (BV) of 0.5 M nitric acid (HNO{sub 3}). The nitric acid eluate, containing the radioactive cesium, would be combined with the sludge from the waste tanks and would be converted into glass at the Defense Waste Processing Facility (DWPF) at SRS. The amount of nitric acid that would be used to elute the RF resin, using the current elution protocol, exceeds the capacity of DWPF to destroy the nitrate ions and maintain the required chemical reducing environment in the glass melt. Installing a denitration evaporator at SRS is technically feasible but would add considerable cost to the project. Alternate methods for eluting the resin have been tested, including using lower concentrations of nitric acid, other acids, and changing the flow regimes. About 4 BV of 0.5 M HNO{sub 3} are required to remove the sodium (titrate the resin) and most of the cesium from the resin, so the bulk of the acid used for the baseline elution method removes a very small quantity of cesium from the resin. A summary of the elution methods that have been tested are listed.

  4. 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.

  5. Biodiesel production using cation-exchange resin as heterogeneous catalyst.

    PubMed

    Feng, Yaohui; He, Benqiao; Cao, Yuhe; Li, Jianxin; Liu, Meng; Yan, Feng; Liang, Xiaoping

    2010-03-01

    Three types of cation-exchange resins (NKC-9, 001 x 7 and D61) as solid acid catalysts were employed to prepare biodiesel from acidified oils generated from waste frying oils. The results show that the catalytic activity of NKC-9 was higher than that of 001 x 7 and D61. The conversion of the esterification by NKC-9 increased with increasing in the amount of catalyst, reaction temperature and time and methanol/oil molar ratio. The maximal conversion of reaction is approximately 90.0%. Furthermore, NKC-9 resin exhibits good reusability. Gas chromatography-mass spectrometry analysis reveals that the production is simplex and mainly composed of C16:0 (palmitic), C18:2 (linoleic), and C18:1 (oleic) acids of methyl ester, respectively. PMID:19699089

  6. EVALUATION OF METHODS FOR THE ISOLATION OR CONCENTRATION OF ORGANIC SUBSTANCES FROM WATER USING XAD-4 QUATERNARY RESIN

    EPA Science Inventory

    A synthetic resin (Amberlite XAD-4 Quaternary in the OH- form) was evaluated as an adsorption medium for the concentration/isolation of acids, amines, aldehydes, carbohydrates, chlorobiphenyls, esters, hydrocarbons, ketones, phenols, polynuclear aromatic hydrocarbons, and trihalo...

  7. Chemically modified polymeric resins for solid-phase extraction and group separation prior to analysis by liquid or gas chromatography

    SciTech Connect

    Schmidt, L.W.

    1993-07-01

    Polystyrene divinylbenzene was modified by acetyl, sulfonic acid, and quaternary ammonium groups. A resin functionalized with an acetyl group was impregnated in a PTFE membrane and used to extract and concentrate phenolic compounds from aqueous samples. The acetyl group created a surface easily wetted, making it an efficient adsorbent for polar compounds in water. The membrane stabilized the resin bed. Partially sulfonated high surface area resins are used to extract and group separate an aqueous mixture of neutral and basic organics; the bases are adsorbed electrostatically to the sulfonic acid groups, while the neutraons are adsorbed hydrophobically. A two-step elution is then used to separate the two fractions. A partially functionalized anion exchange resin is used to separate organic acids and phenols from neutrals in a similar way. Carboxylic acids are analyzed by HPLC and phenols by GC.

  8. 40 CFR Appendix A to Subpart Ddd... - Free Formaldehyde Analysis of Insulation Resins by the Hydroxylamine Hydrochloride Method

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...other phenolic resins, especially those with a high FF content. 2. Principle 2.1a. The basis for this method is the titration of the hydrochloric acid that is liberated when hydroxylamine hydrochloride reacts with formaldehyde to form...

  9. 40 CFR Appendix A to Subpart Ddd... - Free Formaldehyde Analysis of Insulation Resins by the Hydroxylamine Hydrochloride Method

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...other phenolic resins, especially those with a high FF content. 2. Principle 2.1a. The basis for this method is the titration of the hydrochloric acid that is liberated when hydroxylamine hydrochloride reacts with formaldehyde to form...

  10. 40 CFR Appendix A to Subpart Ddd... - Free Formaldehyde Analysis of Insulation Resins by the Hydroxylamine Hydrochloride Method

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...other phenolic resins, especially those with a high FF content. 2. Principle 2.1a. The basis for this method is the titration of the hydrochloric acid that is liberated when hydroxylamine hydrochloride reacts with formaldehyde to form...

  11. Control of resin production in Araucaria angustifolia, an ancient South American conifer.

    PubMed

    Perotti, J C; da Silva Rodrigues-Corrêa, K C; Fett-Neto, A G

    2015-07-01

    Araucaria angustifolia is an ancient slow-growing conifer that characterises parts of the Southern Atlantic Forest biome, currently listed as a critically endangered species. The species also produces bark resin, although the factors controlling its resinosis are largely unknown. To better understand this defence-related process, we examined the resin exudation response of A. angustifolia upon treatment with well-known chemical stimulators used in fast-growing conifers producing both bark and wood resin, such as Pinus elliottii. The initial hypothesis was that A. angustifolia would display significant differences in the regulation of resinosis. The effect of Ethrel(®) (ET - ethylene precursor), salicylic acid (SA), jasmonic acid (JA), sulphuric acid (SuA) and sodium nitroprusside (SNP - nitric oxide donor) on resin yield and composition in young plants of A. angustifolia was examined. In at least one of the concentrations tested, and frequently in more than one, an aqueous glycerol solution applied on fresh wound sites of the stem with one or more of the adjuvants examined promoted an increase in resin yield, as well as monoterpene concentration (?-pinene, ?-pinene, camphene and limonene). Higher yields and longer exudation periods were observed with JA and ET, another feature shared with Pinus resinosis. The results suggest that resinosis control is similar in Araucaria and Pinus. In addition, A. angustifolia resin may be a relevant source of valuable terpene chemicals, whose production may be increased by using stimulating pastes containing the identified adjuvants. PMID:25545585

  12. BENCH SCALE EVALUATION OF RESINS AND ACTIVATED CARBONS FOR WATER PURIFICATION

    EPA Science Inventory

    Adsorption isotherms and bench scale column studies were used to compare the performance of five types of commercially available activated carbon and four types of resin for the removal of humic acids, fulvic acids, 2-methylisoborneol (MIB), and chloroform from water. For the ads...

  13. Method of recovering hazardous waste from phenolic resin filters

    DOEpatents

    Meikrantz, David H. (Idaho Falls, ID); Bourne, Gary L. (Idaho Falls, ID); McFee, John N. (Albuquerque, NM); Burdge, Bradley G. (Idaho Falls, ID); McConnell, Jr., John W. (Idaho Falls, ID)

    1991-01-01

    The invention is a process for the recovery of hazardous wastes such as heavy metals and radioactive elements from phenolic resin filter by a circulating a solution of 8 to 16 molar nitric acid at a temperature of 110 to 190 degrees F. through the filter. The hot solution dissolves the filter material and releases the hazardous material so that it can be recovered or treated for long term storage in an environmentally safe manner.

  14. Poisoning of resin supported catalyst

    SciTech Connect

    Hunter, D.L.; Moore, S.E.

    1987-02-10

    A method is described of enhancing performance of a combined hydroformylation/reduction reaction of an olefin liquid feed in the presence of a resin-supported transition metal complex catalyst. The method comprises: (a) preparing a resin-supported transition metal complex catalyst for use in a combined hydroformylation/reduction reaction substantially free of halides and halide salts in the metal complex catalyst; and (b) introducing an olefin liquid feed to the resin-supported catalyst for conducting a combined hydroformylation/reduction reaction, in the presence of CO and H/sub 2/. The olefin feed has a specified maximum limit of halide concentration sufficiently low to enable continued indefinite operation of the combined hydroformylation/reduction reaction process without halide poisoning.

  15. 21 CFR 872.3140 - Resin applicator.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3140 Resin applicator. (a) Identification. A resin applicator is a brushlike device...

  16. 21 CFR 177.1585 - Polyestercarbonate resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...following specifications: (i) The solution intrinsic viscosity of the polyestercarbonate resins shall be a minimum of 0...per gram, as determined by a method entitled “Intrinsic Viscosity (IV) of Lexan ® Polyestercarbonate Resin by a...

  17. 21 CFR 177.1585 - Polyestercarbonate resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...following specifications: (i) The solution intrinsic viscosity of the polyestercarbonate resins shall be a minimum of 0...per gram, as determined by a method entitled “Intrinsic Viscosity (IV) of Lexan ® Polyestercarbonate Resin by...

  18. 21 CFR 177.1585 - Polyestercarbonate resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...following specifications: (i) The solution intrinsic viscosity of the polyestercarbonate resins shall be a minimum of 0...per gram, as determined by a method entitled “Intrinsic Viscosity (IV) of Lexan ® Polyestercarbonate Resin by...

  19. 21 CFR 177.1655 - Polysulfone resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...the finished resin has a minimum number average molecular weight of 26,000, as determined by osmotic pressure in dimethylformamide. (b) The basic polysulfone resins identified in paragraph (a) of this section may contain optional...

  20. Devices using resin wafers and applications thereof

    DOEpatents

    Lin, YuPo J. (Naperville, IL); Henry, Michael P. (Batavia, IL); Snyder, Seth W. (Lincolnwood, IL); St. Martin, Edward (Libertyville, IL); Arora, Michelle (Woodridge, IL); de la Garza, Linda (Woodridge, IL)

    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.

  1. An investigation of the applicability of the new ion exchange resin, Reillex{trademark}-HPQ, in ATW separations. Milestone 4, Final report

    SciTech Connect

    Ashley, K.R.; Ball, J.; Grissom, M.; Williamson, M.; Cobb, S.; Young, D.; Wu, Yen-Yuan J.

    1993-09-07

    The investigations with the anion exchange resin Reillex{trademark}-HPQ is continuing along several different paths. The topics of current investigations that are reported here are: The sorption behavior of chromium(VI) on Reillex{trademark}-HPQ from nitric acid solutions and from sodium hydroxide/sodium nitrate solutions; sorption behavior of F{sup {minus}} on Reillex{trademark}-HPQ resin in acidic sodium nitrate solution; sorption behavior of Cl{sup {minus}} on Reillex{trademark}-HPQ resin in acidic sodium nitrate solution; sorption behavior of Br{sup {minus}} on Reillex{trademark}-HPQ resin in acidic sodium nitrate solution; and the Honors thesis by one of the students is attached as Appendix II (on ion exchange properties of a new macroperous resin using bromide as the model ion in aqueous nitrate solutions).

  2. Method of removing contaminants from plastic resins

    DOEpatents

    Bohnert,George W. (Harrisonville, MO); Hand,Thomas E. (Lee's Summit, MO); Delaurentiis,Gary M. (Jamestown, CA)

    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.

  3. DIRECT ADAPTIVE CONTROL OF RESIN TRANSFER MOLDING

    E-print Network

    Mamishev, Alexander

    DIRECT ADAPTIVE CONTROL OF RESIN TRANSFER MOLDING B. Minaie1,* , W. Li, J. Gou1 , Y. Chen2 , A. ABSTRACT Resin Transfer Molding (RTM) is a manufacturing process that involves injection of liquid resin into a closed mold cavity containing preset fiber mats and a subsequent curing stage. Mold filling is a crucial

  4. 21 CFR 177.1550 - Perfluorocarbon resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    .... 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...

  5. 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...

  6. 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...

  7. 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...

  8. Method for removing contaminants from plastic resin

    DOEpatents

    Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee's Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

    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.

  9. Method of removing contaminants from plastic resins

    DOEpatents

    Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee's Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

    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.

  10. The many faces of ion-exchange resins

    SciTech Connect

    McNutty, J.T.

    1997-06-01

    Ion-exchange resins have been used commercially for over 60 years. Softening and demineralization of water for boiler feed and process use were then, and continue to be, the most familiar and widespread applications of ion-exchange resins throughout the chemical process industries (CPI). Several types of membrane-based technologies, such as electrodialysis, reverse osmosis and, more recently, electrodeionization are recognized as alternative methods for water treatment. Yet, modern versions of ion-exchange resins remain a major player in water treatment. In addition, these versatile materials can be found performing a wide range of tasks in both aqueous and nonaqueous environments. Some of these diverse applications include: acid or base catalysis; manufacture of high-purity solvents and reagent chemicals; separation of by-products of fermentation processes; deacidification of organic solvents; high-purity water production for semiconductor manufacture; recovery of valuable waste from dilute process effluents; controlled release of pharmaceutical products; and chromatography, both on the analytical and the industrial scale. The key to understanding the potential of ion-exchange resins is to look beyond their exchange and adsorptive characteristics, and to see their fundamental nature. In other words, it`s necessary to first consider them as spherical, particulate reactive polymers that perform chemical reactions.

  11. High Temperature VARTM of Phenylethynyl Terminated Imides (PETI) Resins

    NASA Technical Reports Server (NTRS)

    Ghose, Sayata; Cano, Roberto J.; Britton, Sean M.; Watson, Kent A.; Jensen, Brian J.; Connell, John W.

    2010-01-01

    Fabrication of composite structures using vacuum assisted resin transfer molding (VARTM) is generally more affordable than conventional autoclave techniques. Recent efforts have focused on adapting VARTM for the fabrication of high temperature composites. Due to their low melt viscosity and long melt stability, certain phenylethynyl terminated imides (PETI) can be processed into composites using high temperature VARTM (HT-VARTM). However, one of the disadvantages of the current HT-VARTM resin systems has been the high porosity of the resultant composites. For aerospace applications a void fraction of less than 2% is desired. In the current study, two PETI resins, LARCTM PETI-330 and LARCTM PETI-8 have been used to fabricate test specimens using HT-VARTM. The resins were infused into carbon fiber preforms at 260 C and cured between 316 C and 371 C. Modifications to the thermal cycle used in the laminate fabrication have reduced the void content significantly (typically < 3%) for carbon fiber biaxially woven fabric. Photomicrographs of the panels were taken and void contents were determined by acid digestion. For carbon fiber uniaxial fabric, void contents of less than 2% have been obtained using both PETI-8 and PETI-330. Mechanical properties of the panels were determined at both room and elevated temperatures. These include short beam shear and flexure tests. The results of this work are presented herein.

  12. Resin-infiltrated-dentine--a FE-ESEM microscopy investigation.

    PubMed

    Eick, J D; Dusevich, V M; de Wet, F A; van der Vyver, P J

    2004-09-01

    The formation of a hybrid layer is essential for bonding of dental composites to dentine. The objective of this study was to examine the effects of various etchants/conditioners and dentine bonding systems on dentine surfaces utilising a Field Emission Environmental SEM (FE-ESEM). Twenty one, freshly extracted human molar teeth were utilised. Dentine without resin application was initially observed both wet and dried in the following conditions: (1) fractured surface, (2) smear layer, and (3) smear layer removed with 37% phosphoric acid. Resin infiltration into dentine was then studied after applying Scotchbond 1, Optibond Solo, Prime & Bond NT, or Prompt L-Pop systems. Scotchbond 1, Optibond Solo, and Prime & Bond NT resins penetrated the dentine tubules and created hybrid layers; although, in some cases Prime & Bond NT only created a partially filled hybrid layer. No polymerised resin or hybrid layer was observed for Prompt L-Pop. The FE-ESEM permitted observation of specimens at near in-vivo wet conditions. PMID:15559913

  13. The use of Diphonix{sup {trademark}} ion exchange resin as a preconcentration step for the lanthanides and actinides in analytical applications

    SciTech Connect

    Rollins, A.N.; Thakkar, A.H.; Fern, M.J.

    1995-12-01

    Diphonix ion exchange resin is a chelating ion exchange resin containing sulfonic and gemdiphosphonic acid groups. This resin has a high specificity for the lanthanides and actinides, especially at acidities below pH = 3. Currently, we are investigating new ways to use Diphonix resin as a preconcentration step to separate the lanthanides and actinides from interfering elements present in a variety of environmental matrices. Once the lanthanides and actinides have been separated from the interfering matrix constituents, the elements are removed from the resin and passed through subsequent separation schemes. This presentation will outline the use of Diphonix resin with a variety of problem matrices, and demonstrate its usefulness for analysis of the lanthanides and actinides.

  14. 40 CFR 414.40 - Applicability; description of the thermoplastic resins subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... *ABS-SAN Resins *Acrylate-Methacrylate Latexes *Acrylic Latex *Acrylic Resins *Cellulose Acetate....) Polyethylene Resin, Latex Polyethylene Resins *Polyethylene Resins, Compounded *Polyethylene, Chlorinated... *Polystyrene—Acrylic Latexes Polystyrene Impact Resins Polystyrene Latex Polystyrene, Expandable...

  15. 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... *ABS-SAN Resins *Acrylate-Methacrylate Latexes *Acrylic Latex *Acrylic Resins *Cellulose Acetate Butyrates Cellulose Acetate Resin *Cellulose Acetates *Cellulose Acetates Propionates Cellulose...

  16. 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.

  17. 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.

  18. Synthesis and swelling properties of ?-cyclodextrin-based superabsorbent resin with network structure.

    PubMed

    Huang, Zhanhua; Liu, Shouxin; Fang, Guizhen; Zhang, Bin

    2013-02-15

    A biodegradable, ?-cyclodextrin-based superabsorbent resin was synthesized by the inverse suspension method. The microstructure, chemical structure, and thermal performance of the resin were characterized by scanning electron microscopy, Fourier transform-infrared spectroscopy, and differential scanning calorimetry. The effects of the synthesis conditions (dosage of cross-linking agent, mass ratios of acrylic acid to acrylamide, mass ratios of ?-cyclodextrin to total monomer, neutralization degree, initiator dosage, and reaction time) were optimized to achieve a resin with a maximum swelling capacity. The water absorbency of the optimized resin in distilled water was 1544.76 g/g and that in 0.9 wt.% NaCl was 144.52 g/g. The resin, which is thermoplastic as well as pH-sensitive, had good salt resistance and underwent a maximum in swelling with time in CaCl(2) and AlCl(3) solutions. The fracture surface of the dry resin contained many pores. After swelling, the internal hydrogel showed a typical three-dimensional network structure. The biodegradation of the resin reached 71.2% after 18 days treatment at 30 °C with Lentinus edodes. PMID:23399293

  19. Extraction of High Quality DNA from Seized Moroccan Cannabis Resin (Hashish)

    PubMed Central

    El Alaoui, Moulay Abdelaziz; Melloul, Marouane; Alaoui Amine, Sanaâ; Stambouli, Hamid; El Bouri, Aziz; Soulaymani, Abdelmajid; El Fahime, Elmostafa

    2013-01-01

    The extraction and purification of nucleic acids is the first step in most molecular biology analysis techniques. The objective of this work is to obtain highly purified nucleic acids derived from Cannabis sativa resin seizure in order to conduct a DNA typing method for the individualization of cannabis resin samples. To obtain highly purified nucleic acids from cannabis resin (Hashish) free from contaminants that cause inhibition of PCR reaction, we have tested two protocols: the CTAB protocol of Wagner and a CTAB protocol described by Somma (2004) adapted for difficult matrix. We obtained high quality genomic DNA from 8 cannabis resin seizures using the adapted protocol. DNA extracted by the Wagner CTAB protocol failed to give polymerase chain reaction (PCR) amplification of tetrahydrocannabinolic acid (THCA) synthase coding gene. However, the extracted DNA by the second protocol permits amplification of THCA synthase coding gene using different sets of primers as assessed by PCR. We describe here for the first time the possibility of DNA extraction from (Hashish) resin derived from Cannabis sativa. This allows the use of DNA molecular tests under special forensic circumstances. PMID:24124454

  20. Resin glycosides from the yellow-skinned variety of sweet potato (Ipomoea batatas).

    PubMed

    Rosas-Ramírez, Daniel; Pereda-Miranda, Rogelio

    2013-10-01

    Native to tropical America, Ipomoea batatas has been cultivated for over 5000 years in Mexico. The yellow-skinned tuber crop variety, with an orange flesh, has a higher nutritional value than potato. Raw sweet potato can cause a purge due to its resin glycoside content. Purification of the chloroform-soluble resin glycosides from the roots of this variety was accomplished by preparative-scale HPLC, which allowed for the collection of six oligosaccharides, batatin VII (1) and batatinosides VII-IX (2-4), all of novel structure, together with the known resin glycosides pescaprein I and batatinoside IV. High-field NMR spectroscopy and FAB mass spectrometry were used to characterize each structure, identifying operculinic acid A for compounds 2 and 4, and simonic acid B for 3, as their pentasaccharide glycosidic cores. Batatin VII (1) represents a dimer of the know batatinoside IV, consisting of two units of simonic acid B. PMID:24053411

  1. Regeneration of strong-base anion-exchange resins by sequential chemical displacement

    DOEpatents

    Brown, Gilbert M. (Knoxville, TN); Gu, Baohua (Oak Ridge, TN); Moyer, Bruce A. (Oak Ridge, TN); Bonnesen, Peter V. (Knoxville, TN)

    2002-01-01

    A method for regenerating strong-base anion exchange resins utilizing a sequential chemical displacement technique with new regenerant formulation. The new first regenerant solution is composed of a mixture of ferric chloride, a water-miscible organic solvent, hydrochloric acid, and water in which tetrachloroferrate anion is formed and used to displace the target anions on the resin. The second regenerant is composed of a dilute hydrochloric acid and is used to decompose tetrachloroferrate and elute ferric ions, thereby regenerating the resin. Alternative chemical displacement methods include: (1) displacement of target anions with fluoroborate followed by nitrate or salicylate and (2) displacement of target anions with salicylate followed by dilute hydrochloric acid. The methodology offers an improved regeneration efficiency, recovery, and waste minimization over the conventional displacement technique using sodium chloride (or a brine) or alkali metal hydroxide.

  2. 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.

  3. Oxidative decomposition properties of cationic exchange resins producing SO4(2-) in power plants.

    PubMed

    Zhu, Zhiping; Dai, Chenlin; Liu, Sen; Tian, Ye

    2015-01-01

    The sulphate content of a system increases when strong-acid cationic exchange resins leak into a system or when sulphonic acid groups on the resin organic chain detach. To solve this problem, a dynamic cycle method was used in dissolution experiments of several resins under H2O2 or residual chlorine conditions. Results show that after performing dynamic cycle experiments for 120 hours under oxidizing environments, the SO4(2-) and total organic carbon (TOC) released by four kinds of resins increased with time, contrary to their release velocity. The quantity of released SO4(2-) increased as the oxidizing ability of oxidants was enhanced. Results showed that the quantity and velocity of released SO4(2-) under residual chlorine condition were larger than those under H2O2 condition. Data analysis of SO4(2-) and TOC released from the four kinds of resins by the dynamic cycle experiment revealed that the strength of oxidation resistance of the four resins were as follows: 650C>1500H>S200>SP112H. PMID:26442489

  4. Chemical Characterization of Beer Aging Products Derived from Hard Resin Components in Hops (Humulus lupulus L.).

    PubMed

    Taniguchi, Yoshimasa; Yamada, Makiko; Taniguchi, Harumi; Matsukura, Yasuko; Shindo, Kazutoshi

    2015-11-25

    The bitter taste of beer originates from resins in hops (Humulus lupulus L.), which are classified into two subtypes (soft and hard). Whereas the nature and reactivity of soft-resin-derived compounds, such as ?-, ?-, and iso-?-acids, are well studied, there is only a little information on the compounds in hard resin. For this work, hard resin was prepared from stored hops and investigated for its compositional changes in an experimental model of beer aging. The hard resin contained a series of ?-acid oxides. Among them, 4'-hydroxyallohumulinones were unstable under beer storage conditions, and their transformation induced primary compositional changes of the hard resin during beer aging. The chemical structures of the products, including novel polycyclic compounds scorpiohumulinols A and B and dicyclohumulinols A and B, were determined by HRMS and NMR analyses. These compounds were proposed to be produced via proton-catalyzed cyclization reactions of 4'-hydroxyallohumulinones. Furthermore, they were more stable than their precursor 4'-hydroxyallohumulinones during prolonged storage periods. PMID:26507444

  5. Analysis of the components of hard resin in hops (Humulus lupulus L.) and structural elucidation of their transformation products formed during the brewing process.

    PubMed

    Taniguchi, Yoshimasa; Taniguchi, Harumi; Yamada, Makiko; Matsukura, Yasuko; Koizumi, Hideki; Furihata, Kazuo; Shindo, Kazutoshi

    2014-11-26

    The resins from hops (Humulus lupulus L.), which add the bitter taste to beer, are classified into two main sub-fractions, namely, soft and hard resins. ?- and ?-Acids in soft resin and their transformation during the wort boiling process are well-studied; however, other constituents in resins, especially hard resin, have been unidentified. In this study, we identified humulinones and hulupones as soft-resin components, in addition to 4'-hydroxyallohumulinones and tricyclooxyisohumulones A and B as hard-resin components. These compounds are all oxidation products derived from ?- or ?-acids. We also investigated compositional changes in the hard resin during the wort boiling process, which has a significant effect on the taste of the beer, by using model boiling experiments. The major changes were identified to be isomerization of 4'-hydroxyallohumulinones into 4'-hydroxyallo-cis-humulinones, followed by decomposition into cis-oxyhumulinic acids. These findings will be helpful in systematically evaluating and optimizing the effect of the hard resin on beer quality. PMID:25354357

  6. Etching conditions for resin-modified glass ionomer cement for orthodontic brackets.

    PubMed

    Valente, Rudolfo M; De Rijk, Waldemar G; Drummond, James L; Evans, Carla A

    2002-05-01

    This study reports the tensile bond strength of orthodontic eyelets (RMO, Inc, Denver, Colo) bonded to human extracted teeth with a resin-modified glass ionomer cement (RMGIC) (Fuji Ortho LC, GC America, Alsip, Ill) and various acid etchants (Etch-37 and All-Etch, Bisco, Schaumburg, Ill; Ultra Etch, 3M Unitek, St Paul, Minn) for enamel preparation before bonding. The enamel etch conditions were as follows: 37% phosphoric acid with silica; 37% phosphoric acid, silica-free; 10% phosphoric acid, silica-free; 10% polyacrylic acid; and unetched enamel. Bond strength was measured by pulling in tension on the eyelet with a 0.018-in steel wire perpendicular to the enamel surface with a testing machine (Instron model 1125, Canton, Mass) at a speed of 2 mm/min. A light-cured resin cement (Transbond XT, 3M Unitek, Monrovia, Calif) applied to enamel etched with 37% phosphoric acid containing silica served as a control. Each group included 30 specimens. The Weibull distribution (m) was used for statistical analysis with a 90% CI. The different etchants used with RMGIC did not affect tensile bond strength. The resin cement group had the highest tensile strength. Significantly lower bond strengths were observed when glass ionomer cement was used to bond orthodontic attachments to nonetched teeth. However, unlike resin cement, RMGIC can bond effectively to etched teeth in a moist environment without an additional bonding agent. PMID:12045770

  7. Phenol-formaldehyde resin substitutes from biomass tars

    SciTech Connect

    Himmelblau, D.A.

    1995-11-01

    Approximately 320,000 tonnes of phenol and formaldehyde are currently used annually in North America to make adhesive resins that are used to make exterior-grade structural panels. The demand for phenol-formaldehyde (PF) resins is growing faster than the demand for panels, because more adhesive is required to join/coat the surface of wood flakes (for oriented strand board - OSB) than is required to join veneer; OSB is replacing plywood as logs large enough for veneer become scarcer. Also, competitive uses for phenol and methanol (for making formaldehyde) have increased raw materials cost and threatened availability. Production of adhesive resins from biomass to reduce reliance on raw materials derived from commodity petrochemicals and to lower resin cost looks attractive. A simple fluidized-bed reactor system can be used to produce tars that can substitute for a major portion of the phenol and formaldehyde in PF resin adhesives. This can be done in an air-fluidized, single-bed reactor; no inert gas or dual-bed system is required. The key is recognizing that optimum phenolic character in the tar is not produced at the maximum tar yield, but at reactor temperatures around 600{degrees}C and short gas-phase residence times that produce a yield of about 25 to 30 weight percent. A wide range of phenols, aldehydes and other compounds capable of polymerization are produced. Feedstock can be any wood waste larger than sander dust; low cost agricultural wastes such as bagasse are also suitable. Adhesive resin is produced from the entire tar product by shifting the pH from acidic to basic with NaOH, and combining and heating the resulting resole with phenol and formaldehyde, similarly to conventional resins. Approximately half of the phenol and formaldehyde by weight can be replaced with tar. A plant producing 13,865,000 kg (30,566,000 lb) annually from 308 tonnes (340 tons) per day of green wood chips would cost approximately $8,400,000.

  8. 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.

  9. Separation of Lanthanide Ions with Kläui Ligand Resin

    SciTech Connect

    Granger, Trinity D.; Henry, Victoria A.; Latesky, Stanley

    2007-07-01

    Separation and pre-concentration of the desired analyte is often a critical step in many radioanalytical methods. Current procedures for separating and concentrating analytes for detection are complex, and can be both expensive and time consuming. Therefore, the purpose of this research is to develop an alternative method of separating lanthanide ions through the use of an extraction chromatography resin containing a Klaui ligand salt. This research is a continuation of a concerted effort to develop new methods of detecting small concentrations of radionuclides and lanthanides using Klaui ligands. The Klaui ligands, C5Me5Co(OP(OR)2)3- (R=Me, Et, n-Pr) (LOR-), have unique affinity for lanthanide and actinide ions in the presence of competing metal ions. The use of 1 wt% NaLOR (R=Et or n-Pr) adsorbed onto resin support has been shown to extract lanthanide ions from aqueous nitric acid solutions of different concentrations. In order to further evaluate the utility of these materials in radiochemical separation, the selectivity of the resins for the different lanthanide ions was examined by measuring the distribution coefficients (Kd) for a series of lanthanides over a range of solution conditions. Based on prior research with actinide ions, it was hypothesized that the lanthanide ions would bond strongly with the Klaui ligands. The success of this research is important, because it will assist in expanding and improving current automated radiochemical methods, which will decrease the cost of developing and implementing radiochemical methods. To date, Kd values have been determined for Eu+3, Nd+3 and Pr+3 under varying nitric acid (HNO3) concentration, using a resin consisting of 1.0 wt% NaLOPr on Amberlite XAD-7HP. The dependence of the Kd values for Eu+3 has also been examined as a function of the ligand-to-europium ratio and the nitrate concentration. Decreasing Kd values were obtained upon increasing the nitric acid concentration, indicating protonation of the ligand, which competes with binding of the lanthanide ions. As expected, increasing the Klaui ligand-to-europium ratio results in increasing Kd, but no conclusions could be made from these data regarding stoichiometry of the complex formed on the resin. No dependence of the Kd on the nitrate concentration was observed, supporting the notion that the HNO3 dependence is dominated by the presence of the acidic hydronium ion (as opposed to the nitrate ion). Future work will involve the determination of the Kd values for the remainder of the lanthanide series to further assess the potential of the Klaui ligand for intra-group lanthanide separations.

  10. Removal of cadmium from fish sauce using chelate resin.

    PubMed

    Sasaki, Tetsuya; Araki, Ryohei; Michihata, Toshihide; Kozawa, Miyuki; Tokuda, Koji; Koyanagi, Takashi; Enomoto, Toshiki

    2015-04-15

    Fish sauce that is prepared from squid organs contains cadmium (Cd), which may be present at hazardous concentrations. Cd molecules are predominantly protein bound in freshly manufactured fish sauce, but are present in a liberated form in air-exposed fish sauce. In the present study, we developed a new method for removing both Cd forms from fish sauce using chelate resin and a previously reported tannin treatment. Sixteen-fold decreases in Cd concentrations were observed (0.78-0.05 mg/100 mL) following the removal of liberated Cd using chelate resin treatment, and the removal of protein-bound Cd using tannin treatment. Major nutritional components of fish sauce were maintained, including free amino acids and peptides, and angiotensin I-converting enzyme inhibitory and antioxidant activities. PMID:25466035

  11. Accurate determination of ¹²?I concentrations and ¹²?I/¹³?Cs ratios in spent nuclear resins by Accelerator Mass Spectrometry.

    PubMed

    Nottoli, Emmanuelle; Bienvenu, Philippe; Labet, Alexandre; Bourlès, Didier; Arnold, Maurice; Bertaux, Maité

    2014-04-01

    Determining long-lived radionuclide concentrations in radioactive waste has fundamental implications for the long-term management of storage sites. This paper focuses on the measurement of low (129)I contents in ion exchange resins used for primary fluid purification in Pressurised Water Reactors (PWR). Iodine-129 concentrations were successfully determined using Accelerator Mass Spectrometry (AMS) following a chemical procedure which included (1) acid digestion of resin samples in HNO3/HClO4, (2) radioactive decontamination by selective iodine extraction using a new chromatographic resin (CL Resin), and (3) AgI precipitation. Measured (129)I concentrations ranged from 4 to 12 ng/g, i.e. from 0.03 to 0.08 Bq/g. The calculation of (129)I/(137)Cs activity ratios used for routine waste management produced values in agreement with the few available data for PWR resin samples. PMID:24525301

  12. Petroleum resins and their production

    SciTech Connect

    Luvinh, Q.

    1989-04-25

    A process is described for the production of petroleum resins compatible with base polymers in hot melt formulations and having a softening point of from about 60/sup 0/C. to about 120/sup 0/C. and Gardner color of about 4 or less, comprising copolymerizing using a Friedel-Crafts catalyst. The mixture is substantially free form cyclopentadiene and dicyclopentadiene. This patent also describes a resin consisting essentially of a copolymer containing from 5 to 80 wt. % of units derived from an olefinically unsaturated aromatic compound form 5 to 80 wt. % of units derived from C/sub 5/ olefines or diolefines or C/sub 6/ olefines diolefines or a mixture of C/sub 5/ and C/sub 6/ olefines or diolefines and from 7 to 45 wt. % of units derived from a terpene.

  13. Factorial experimental design for recovering heavy metals from sludge with ion-exchange resin.

    PubMed

    Lee, I Hsien; Kuan, Yu-Chung; Chern, Jia-Ming

    2006-12-01

    Wastewaters containing heavy metals are usually treated by chemical precipitation method in Taiwan. This method can remove heavy metals form wastewaters efficiently, but the resultant heavy metal sludge is classified as hazardous solid waste and becomes another environmental problem. If we can remove heavy metals from sludge, it becomes non-hazardous waste and the treatment cost can be greatly reduced. This study aims at using ion-exchange resin to remove heavy metals such as copper, zinc, cadmium, and chromium from sludge generated by a PCB manufacturing plant. Factorial experimental design methodology was used to study the heavy metal removal efficiency. The total metal concentrations in the sludge, resin, and solution phases were measured respectively after 30 min reaction with varying leaching agents (citric acid and nitric acid); ion-exchange resins (Amberlite IRC-718 and IR-120), and temperatures (50 and 70 degrees C). The experimental results and statistical analysis show that a stronger leaching acid and a higher temperature both favor lower heavy metal residues in the sludge. Two-factors and even three-factor interaction effects on the heavy metal sorption in the resin phase are not negligible. The ion-exchange resin plays an important role in the sludge extraction or metal recovery. Empirical regression models were also obtained and used to predict the heavy metal profiles with satisfactory results. PMID:16843592

  14. Haemostatic agents on the shear bond strength of self-adhesive resin

    PubMed Central

    Anil, Akansha; Sekhar, Anand; Ginjupalli, Kishor

    2015-01-01

    Background Dentin surface contaminated with haemostatic agents can interfere with the bonding of self-adhesive resin cement. Therefore the purpose of this study was to evaluate the effect of various haemostatic agents such as Aluminium chloride, Ferric sulphate and Tannic acid on the shear bond strength of self-adhesive resin luting agent. Material and Methods The buccal surfaces of extracted premolars were flattened to expose the dentine. The teeth were then randomly divided into four groups. In Group I Aluminium Chloride was applied on the flattened dentinal surface, in Group II Ferric Sulphate was applied to exposed dentin surface, in Group III tannic acid was applied on to the dentinal surface, and the control group, i.e. Group IV was rinsed with saline. After the surface treatment, all the teeth were air dried. Then a predetermined dimension of RelyX™ U200 self-adhesive resin cement was bonded to the pretreated dentin surfaces. The samples were then stored under 370C in distilled water for 24 hours under 100 % humidity. Following this each sample was tested for shear bond strength with an Instron testing machine at a crosshead speed of 1mm/min. Results There was significant difference in the shear bond strength of control and tannic acid contaminated group (p<0.05), whereas there was no significant differences between the shear bond strength between control and aluminium chloride and ferric sulphate groups (p>0.05). Conclusions The usage of haemostatic agent can negatively affect the bond strength of self-adhesive resin cement (Rely X) on to the dentin surface. As per the study Tannic acid significantly weakened the bond between the self-adhesive resin and dentin. Key words:Aluminium chloride, Ferric sulphate, haemostatic agent, self-adhesive resin cement, shear bond strength, Tannic acid. PMID:26330930

  15. Phosphorus-containing imide resins

    NASA Technical Reports Server (NTRS)

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

    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.

  16. Evaluation of adhesion of reline resins to the thermoplastic denture base resin for non-metal clasp denture.

    PubMed

    Kim, Ji Hye; Choe, Han Cheol; Son, Mee Kyoung

    2014-01-01

    This study aimed to evaluate the tensile and transverse bond strength of chairside reline resins (Tokuyama Rebase II, Mild Rebaron LC) to a thermoplastic acrylic resin (Acrytone) used for non metal clasp denture. The results were compared with those of a conventional heat polymerized acrylic resin (Paladent 20) and a thermoplastic polyamide resin (Biotone). The failure sites were examined by scanning electron microscopy to evaluate the mode of failure. As results, the bond strength of reline resins to a thermoplastic acrylic resin was similar to the value of a conventional heat polymerized acrylic resin. However, thermoplastic polyamide resin showed the lowest value. The results of this study indicated that a thermoplastic acrylic resin for non metal clasps denture allows chairside reline and repair. It was also found that the light-polymerized reline resin had better bond strength than the autopolymerizing reline resin in relining for a conventional heat polymerized acrylic resin and a thermoplastic acrylic resin. PMID:24492109

  17. 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.

  18. 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.

  19. 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.

  20. 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

  1. 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.

  2. 21 CFR 175.380 - Xylene-formaldehyde resins condensed with 4,4?-isopropylidenediphenol-epichlorohydrin epoxy resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...-isopropylidenediphenol-epichlorohydrin epoxy resins. 175.380 Section 175.380 Food and Drugs FOOD AND DRUG ADMINISTRATION... Xylene-formaldehyde resins condensed with 4,4?-isopropylidenediphenol-epichlorohydrin epoxy resins. The...) The resins are produced by the condensation of xylene-formaldehyde resin and...

  3. Sulfate ion (SO4(2-)) release from old and new cation exchange resins used in condensate polishing systems for power plants.

    PubMed

    Zhu, Zhi-Ping; Tang, Xue-Ying; Yin, Zhao-Hui; Yu, Wei-Wei

    2014-01-01

    In this study, a dynamic cycle test, a static immersion method and a pyrolysis experiment were combined to examine the characteristics of SO4(2-) released from several new and old cation exchange resins used in condensate polishing systems for power plants. The results show that the quantity and velocity of SO4(2-) released from new and old resins tend to balance in a short time during the dynamic cycle experiment. SO4(2-) is released by 1500H (monosphere super gel type cation exchange resins) and 001 × 7 (gel type cation exchange resins) new and old cation exchange resins, the quantity of which increases according to immersion time. In the pyrolysis experiment, the quantity of SO4(2-) released from resins increases and the pH of the pyrolysis solution transforms from alkaline to acidic with an increase in temperature. PMID:25325543

  4. Development of vibration-damping resins for room-temperature application

    NASA Astrophysics Data System (ADS)

    Taniuchi, Mamoru; Takatsuka, Kohro; Fujiwara, Haruo; Korida, Kazuhiko

    1991-03-01

    Copolymers of vinyl acetate, n-butyl acrylate, VeoVa 10, and acrylic acid were prepared in order to develop new high vibration-damping resins for vibration-damping composite steel sheets for room-temperature application. The characteristics of the resins were affected by the properties of each monomer used. Vinyl acetate and n-butyl acrylate were known to have good vibration-damping properties around room temperatures. We found that VeoVa 10 had a pronounced effect on the lowering of the melt viscosity. Acrylic acid was added to improve the adhesion performance with steel sheets. The composite steel sheets produced using these resins exhibited a high loss factor of approximately 0.3 to 0.4 at 20 °C to 30 °C and 250 Hz. The melt viscosity was in the 5 to 20 Pa · s range at 180 °C.

  5. Development of solvent-free offset ink using vegetable oil esters and high molecular-weight resin.

    PubMed

    Park, Jung Min; Kim, Young Han; Kim, Sung Bin

    2013-01-01

    In the development of solvent-free offset ink, the roles of resin molecular weight and used solvent on the ink performance were evaluated by examining the relationship between the various properties of resin and solvent and print quality. To find the best performing resin, the soy-oil fatty acid methyl ester (FAME) was applied to the five modified-phenolic resins having different molecular weights. It is found from the experimental results that the ink made of higher molecular weight and better solubility resin gives better printability and print quality. It is because larger molecular weight resin with better solubility gives higher rate of ink transfer. From the ink application of different esters to high molecular weight resin, the best printing performance was yielded from the soy-oil fatty acid butyl ester (FABE). It is due to its high kinematic viscosity resulting in the smallest change of ink transfer weight upon multiple number of printing, which improves the stability of ink quality. PMID:23728325

  6. 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.

  7. Graphite composites with advanced resin matrices

    NASA Technical Reports Server (NTRS)

    Kourtides, D. A.

    1980-01-01

    The effect of processing variables on the flammability and mechanical properties for state-of-the-art and advanced resin matrices for graphite composites were studied. Resin matrices which were evaluated included state-of-the-art epoxy, phenolic-novolac, phenolic-xylok, two types of bismaleimides, benzyl, polyethersulfone, and poly(p-phenylene sulfone). Comparable flammability and thermochemical data on graphite-reinforced laminates prepared with these resin matrices are presented, and the relationship of some of these properties to the anaerobic char yield of the resins is described.

  8. Microbiological Study of Water-Softener Resins

    PubMed Central

    Stamm, John M.; Engelhard, Warren E.; Parsons, James E.

    1969-01-01

    Microbial identification using effluents backflushed from exhausted urban and rural tank resins and cleaned resins containing the sulfonated copolymer of styrene and divinylbenzene (SDB) were completed, along with microbial assessment of the concentrated stock salt brine. Forty-four different bacterial and fungal genera were identified. Extensive biochemical and animal virulence tests completed on one of the six bacterial salt brine isolates indicated a pathogenic staphylococcal strain. The retention of Staphylococcus aureus, a Flavobacterium sp, and Escherichia coli B bacteriophage was demonstrated both by using the nonexhausted sodium-regenerated resin and by using the same resin exchanged with different mono-, di-, and trivalent cations. Effluent counts completed after bacterial seepage through the resins indicated the Pb++ exchanged resin removed 55% of the bacteria; Na+, Fe++, and Al+++ removed 31 to 36% and Ca++ and Cu++ removed about 10 to 15%. Seventy per cent or more of the bacteriophage was removed by Fe++, Cu++, and Al+++, whereas the Ca++ and Na++ cations removed 25 to 31%. Over a 77-day period, nonsterile tap water was passed through bacterial seeded and uninoculated SDB (Na) resin columns. Effluent and resin elution counts demonstrated the growth and survival of 2 different bacteria per column. Increased bacterial retention, survival, and multiplication occurred concomitantly with accumulation of organic and inorganic materials and the Ca++ and Mg++ cations from the tap water. Furthermore, microbial elution from resin particles taken from column depths of 1, 8, and 16 cm indicated a bacterial diminution with increasing depths. PMID:5373675

  9. Flexible heat resistant neutron shielding resin

    NASA Astrophysics Data System (ADS)

    Sukegawa, Atsuhiko M.; Anayama, Yoshimasa; Okuno, Koichi; Sakurai, Shinji; Kaminaga, Atsushi

    2011-10-01

    A flexible heat resistant neutron shielding material has been developed, which consists of polymer resin with 1 wt% boron. The neutron shielding performance of the developed resin, examined by the 252Cf neutron source, is almost the same as that of the polyethylene. The outgas of H 2, H 2O, CO and CO 2 from the resin have been measured at ˜250 °C environment. The resin will be applied around the port of the vacuum vessel as an additional shielding material and reduce the neutron streaming from a superconducting tokamak device such as JT-60SA.

  10. 21 CFR 177.1600 - Polyethylene resins, carboxyl modified.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...2010-04-01 2009-04-01 true Polyethylene resins, carboxyl modified. 177...Contact Surfaces § 177.1600 Polyethylene resins, carboxyl modified. Carboxyl-modified polyethylene resins may be safely used as...

  11. 40 CFR 721.4380 - Modified hydrocarbon resin.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 2012-07-01 false Modified hydrocarbon resin. 721.4380 Section 721...Substances § 721.4380 Modified hydrocarbon resin. (a) Chemical substance...identified generically as a modified hydrocarbon resin (P-91-1418) is...

  12. 40 CFR 721.4380 - Modified hydrocarbon resin.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 2013-07-01 false Modified hydrocarbon resin. 721.4380 Section 721...Substances § 721.4380 Modified hydrocarbon resin. (a) Chemical substance...identified generically as a modified hydrocarbon resin (P-91-1418) is...

  13. 40 CFR 721.4380 - Modified hydrocarbon resin.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 2014-07-01 false Modified hydrocarbon resin. 721.4380 Section 721...Substances § 721.4380 Modified hydrocarbon resin. (a) Chemical substance...identified generically as a modified hydrocarbon resin (P-91-1418) is...

  14. 40 CFR 721.4380 - Modified hydrocarbon resin.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 2011-07-01 false Modified hydrocarbon resin. 721.4380 Section 721...Substances § 721.4380 Modified hydrocarbon resin. (a) Chemical substance...identified generically as a modified hydrocarbon resin (P-91-1418) is...

  15. 40 CFR 721.4380 - Modified hydrocarbon resin.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 2010-07-01 false Modified hydrocarbon resin. 721.4380 Section 721...Substances § 721.4380 Modified hydrocarbon resin. (a) Chemical substance...identified generically as a modified hydrocarbon resin (P-91-1418) is...

  16. 21 CFR 177.2355 - Mineral reinforced nylon resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...2014-04-01 2014-04-01 false Mineral reinforced nylon resins. 177.2355 Section 177.2355 Food...Repeated Use § 177.2355 Mineral reinforced nylon resins. Mineral reinforced nylon resins identified in paragraph (a) of...

  17. 21 CFR 177.2355 - Mineral reinforced nylon resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...2013-04-01 2013-04-01 false Mineral reinforced nylon resins. 177.2355 Section 177.2355 Food...Repeated Use § 177.2355 Mineral reinforced nylon resins. Mineral reinforced nylon resins identified in paragraph (a) of...

  18. 21 CFR 177.2355 - Mineral reinforced nylon resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...2012-04-01 2012-04-01 false Mineral reinforced nylon resins. 177.2355 Section 177.2355 Food...Repeated Use § 177.2355 Mineral reinforced nylon resins. Mineral reinforced nylon resins identified in paragraph (a) of...

  19. 21 CFR 872.3820 - Root canal filling resin.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 2012-04-01 2012-04-01 false Root canal filling resin. 872.3820 Section...DEVICES Prosthetic Devices § 872.3820 Root canal filling resin. (a) Identification. A root canal filling resin is a device...

  20. 21 CFR 872.3820 - Root canal filling resin.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 2014-04-01 2014-04-01 false Root canal filling resin. 872.3820 Section...DEVICES Prosthetic Devices § 872.3820 Root canal filling resin. (a) Identification. A root canal filling resin is a device...

  1. 40 CFR 721.2752 - Epoxy resin containing phosphorus (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...2014-07-01 false Epoxy resin containing phosphorus (generic). 721.2752 Section...721.2752 Epoxy resin containing phosphorus (generic). (a) Chemical substance...generically as an epoxy resin containing phosphorus (PMN P-00-912) is subject...

  2. 40 CFR 721.2752 - Epoxy resin containing phosphorus (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...2012-07-01 false Epoxy resin containing phosphorus (generic). 721.2752 Section...721.2752 Epoxy resin containing phosphorus (generic). (a) Chemical substance...generically as an epoxy resin containing phosphorus (PMN P-00-912) is subject...

  3. 40 CFR 721.2752 - Epoxy resin containing phosphorus (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...2010-07-01 false Epoxy resin containing phosphorus (generic). 721.2752 Section...721.2752 Epoxy resin containing phosphorus (generic). (a) Chemical substance...generically as an epoxy resin containing phosphorus (PMN P-00-912) is subject...

  4. 40 CFR 721.2752 - Epoxy resin containing phosphorus (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...2011-07-01 false Epoxy resin containing phosphorus (generic). 721.2752 Section...721.2752 Epoxy resin containing phosphorus (generic). (a) Chemical substance...generically as an epoxy resin containing phosphorus (PMN P-00-912) is subject...

  5. 40 CFR 721.2752 - Epoxy resin containing phosphorus (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...2013-07-01 false Epoxy resin containing phosphorus (generic). 721.2752 Section...721.2752 Epoxy resin containing phosphorus (generic). (a) Chemical substance...generically as an epoxy resin containing phosphorus (PMN P-00-912) is subject...

  6. 21 CFR 177.2355 - Mineral reinforced nylon resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 3 2010-04-01 2009-04-01 true Mineral reinforced nylon resins. 177.2355 Section...Articles Intended for Repeated Use § 177.2355 Mineral reinforced nylon resins. Mineral reinforced nylon resins identified in...

  7. 21 CFR 177.2510 - Polyvinylidene fluoride resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...2010-04-01 2009-04-01 true Polyvinylidene fluoride resins. 177.2510 Section 177.2510...Repeated Use § 177.2510 Polyvinylidene fluoride resins. Polyvinylidene fluoride resins may be safely used as articles...

  8. Chemical affinities between the solvent extractable and the bulk organic matter of fossil resin associated with an extinct podocarpaceae

    USGS Publications Warehouse

    Grimalt, J.O.; Simoneit, B.R.T.; Hatcher, P.G.

    1989-01-01

    Analyses by GC-MS and GC-IR of resin associated to Dacridiumites mawsonii deposits, an extinct species of Podocarpaceae occurring on the South Island of New Zealand during the Bortonian (Middle Eocene), have revealed that dehydroabietic acid is the predominant component of the solvent soluble fraction. Accordingly, this diterpenoid has been selected as the principal component material for spectroscopic comparison with the bulk resin using IR and CP/MAS 13C NMR. ?? 1989.

  9. Synthesis and characterization of amphoteric resins and its use for treatment of radioactive liquid waste

    SciTech Connect

    Siyam, T.; El-Naggar, I.M.; Aly, H.F.

    1996-12-31

    Amphoteric resins such as poly (acrylamide-acrylic acid-diallylamine-hydrochloride) {open_quotes}P(AH-AA-DAA){sup +}Cl{close_quotes} and poly (acrylamide-acrylic acid-dially-ethylamine-hydrochloride) {open_quotes}P(AM-AA-DAEA){sup +} Cl{close_quotes} were prepared by gamma radiation-induced polymerization of acrylic acid {open_quotes}AA{close_quotes} in the presence of poly(amidoamines) such as poly(acryl-amide-diallyamine-hydrochloride) {open_quotes}P(AM- DAAH){sup +}Cl{close_quotes} and poly(acrylamide-dially-ethylamine-hydrochloride){close_quotes}P(AM-DAEAH){sup +} Cl{sup -}{close_quotes} it as template polymers using a template polymerization technique. Spectroscopic studies showed that resins contain both amide- and carboxylic groups, and the peak of {r_angle}NH of amine salts at (3000-2700 cm{sup {minus}1}) and (2700-2500 cm{sup {minus}1}) is disappeared. This indicates that the addition of acrylic acid monomer on ammonium groups. These ammonium groups in template polymers are converted into acrylic acid chain ends in the obtained resins accordingly, the probability of the polymer degradation of decreases may be attributed to the high radiation stability of these chain ends of acrylic acid units. The capacities of the obtained resins increase by increasing the absorbed doses of about {approximately}20 kGy, but at high doses the capacities decrease. On increasing the amines ratio in template polymers the capacities of resins for cation decreased but increased for anions. The capacities of the product materials to some heavy metal ions decrease with increasing the hydrogen ion concentrations and the selectivity is decreased in the order Cu{sup 2+} > Co{sup 2+} > Cs{sup +}.

  10. 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 strength), and about 78% (shear strain to failure) relative to the control composite.

  11. Effect of resin rheology on macro- and micro-flows in resin transfer molding

    SciTech Connect

    Chih-Hsin Shih; Lee, L.J.; Koelling, K.

    1996-12-31

    Resin transfer molding (RTM) is a relatively new and high potential process for near net shape composite manufacturing because of its short cycle time, low labor requirements and low equipment cost. The major material variables in the RTM process are the resin rheology and the fiber reinforcement structure. The presence of low profile additives or fillers tends to change the resin mixture from a Newtonian fluid to a Non-Newtonian fluid. Different fiber architectures may result in different flow patterns that will influence the mold filling and curing processes. This paper will discuss how the resin rheology and fiber structure effect the resin transfer molding process.

  12. 21 CFR 175.320 - Resinous and polymeric coatings for polyolefin films.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... film over one or both sides of a base film produced from one or more of the basic olefin polymers complying with § 177.1520 of this chapter. The base polyolefin film may contain optional adjuvant substances... Limitations (i) Resins and polymers: Acrylic acid polymer and its ethyl or methyl esters...

  13. 21 CFR 175.320 - Resinous and polymeric coatings for polyolefin films.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... coating is applied as a continuous film over one or both sides of a base film produced from one or more of the basic olefin polymers complying with § 177.1520 of this chapter. The base polyolefin film may... as are provided: List of substances Limitations (i) Resins and polymers: Acrylic acid polymer and...

  14. 21 CFR 175.320 - Resinous and polymeric coatings for polyolefin films.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... coating is applied as a continuous film over one or both sides of a base film produced from one or more of the basic olefin polymers complying with § 177.1520 of this chapter. The base polyolefin film may... as are provided: List of substances Limitations (i) Resins and polymers: Acrylic acid polymer and...

  15. 21 CFR 175.320 - Resinous and polymeric coatings for polyolefin films.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... coating is applied as a continuous film over one or both sides of a base film produced from one or more of the basic olefin polymers complying with § 177.1520 of this chapter. The base polyolefin film may... as are provided: List of substances Limitations (i) Resins and polymers: Acrylic acid polymer and...

  16. 21 CFR 175.320 - Resinous and polymeric coatings for polyolefin films.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... coating is applied as a continuous film over one or both sides of a base film produced from one or more of the basic olefin polymers complying with § 177.1520 of this chapter. The base polyolefin film may... as are provided: List of substances Limitations (i) Resins and polymers: Acrylic acid polymer and...

  17. Biotinylation of Amino Group 1. Wash 0.1 mmol resin with DMF.

    E-print Network

    Yao, Shao Q

    x). 8. Let the resin dry before proceeding to cleavage. Synthesis of Phosphotyrosine-Containing Peptides Using Fmoc-Phosphotyrosine Reagent: N--Fmoc-O-phosphotyrosine [1 g, AnaSpec Catalog # 20254; 5 g incomplete coupling. 5. Increase the coupling time of the amino acid residues after the phosphotyrosine

  18. 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.

  19. 21 CFR 175.320 - Resinous and polymeric coatings for polyolefin films.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...percent of the polymer. The polymer number average molecular weight...The acid number of the polymer shall be less than 250. The...Terpene resins consisting of polymers of ?-pinene, ?-pinene...as an antimicrobial agent in emulsion-based silicone...

  20. 21 CFR 175.320 - Resinous and polymeric coatings for polyolefin films.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...percent of the polymer. The polymer number average molecular weight...The acid number of the polymer shall be less than 250. The...Terpene resins consisting of polymers of ?-pinene, ?-pinene...as an antimicrobial agent in emulsion-based silicone...

  1. Manual and automated synthesis Manual synthesis of a resin-bound pentapeptide library 6

    E-print Network

    Yao, Shao Q

    Manual and automated synthesis Manual synthesis of a resin-bound pentapeptide library 6 Automated construction of an organic library using split synthesis: 3-amino-5-hydroxybenzoic acid as a core structure 10 Synthetic strategies for library construction Portioning-mixing synthesis of a library encoded

  2. Phosphorus-containing imide resins

    NASA Technical Reports Server (NTRS)

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

    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. 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 additional government-funded testing proved that RP-46 is even more exceptional than originally thought.

  4. Zoledronate and ion-releasing resins impair dentin collagen degradation.

    PubMed

    Tezvergil-Mutluay, A; Seseogullari-Dirihan, R; Feitosa, V P; Tay, F R; Watson, T F; Pashley, D H; Sauro, S

    2014-10-01

    This study analyzed the amounts of solubilized telopeptides cross-linked carboxyterminal telopeptide of type I collagen (ICTP) and C-terminal crosslinked telopeptide of type I collagen (CTX) derived from matrix-metalloproteinases (MMPs) and cysteine cathepsins (CTPs) subsequent to application of a filler-free (Res.A) or an ion-releasing resin (Res.B) to ethylenediaminetetraacetic acid (EDTA)-demineralized dentin with or without zoledronate-containing primer (Zol-primer) pre-treatment. The chemical modification induced following treatments and artificial saliva (AS) storage was also analyzed through attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR). Totally EDTA-demineralized specimens were infiltrated with Res.A or Res.B with or without Zol-primer pre-treatment, light-cured, and immersed in AS for up to 4 wk. ICTP release was reduced following infiltration with Res.B and further reduced when Res.B was used with Zol-primer; remarkable phosphate mineral uptake was attained after AS storage. CTX release was increased in Res.A- and Res.B-treated dentin. However, when Zol-primer was used with Res.A, the CTX release fell significantly compared to the other tested resin-infiltration methods. In conclusion, zoledronate offers an additional inhibitory effect to the ion-releasing resins in MMP-mediated collagen degradation. However, Zol-primer induces a modest reduction in CTX release only when used with resin-based systems containing no ion-releasing fillers. PMID:25074494

  5. Zoledronate and Ion-releasing Resins Impair Dentin Collagen Degradation

    PubMed Central

    Tezvergil-Mutluay, A.; Seseogullari-Dirihan, R.; Feitosa, V.P.; Tay, F.R.; Watson, T.F.; Pashley, D.H.; Sauro, S.

    2014-01-01

    This study analyzed the amounts of solubilized telopeptides cross-linked carboxyterminal telopeptide of type I collagen (ICTP) and C-terminal crosslinked telopeptide of type I collagen (CTX) derived from matrix-metalloproteinases (MMPs) and cysteine cathepsins (CTPs) subsequent to application of a filler-free (Res.A) or an ion-releasing resin (Res.B) to ethylenediaminetetraacetic acid (EDTA)-demineralized dentin with or without zoledronate-containing primer (Zol-primer) pre-treatment. The chemical modification induced following treatments and artificial saliva (AS) storage was also analyzed through attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR). Totally EDTA-demineralized specimens were infiltrated with Res.A or Res.B with or without Zol-primer pre-treatment, light-cured, and immersed in AS for up to 4 wk. ICTP release was reduced following infiltration with Res.B and further reduced when Res.B was used with Zol-primer; remarkable phosphate mineral uptake was attained after AS storage. CTX release was increased in Res.A- and Res.B-treated dentin. However, when Zol-primer was used with Res.A, the CTX release fell significantly compared to the other tested resin-infiltration methods. In conclusion, zoledronate offers an additional inhibitory effect to the ion-releasing resins in MMP-mediated collagen degradation. However, Zol-primer induces a modest reduction in CTX release only when used with resin-based systems containing no ion-releasing fillers. PMID:25074494

  6. 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.

  7. Fluorinated diamond bonded in fluorocarbon resin

    DOEpatents

    Taylor, Gene W. (Los Alamos, NM)

    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.

  8. 21 CFR 177.1550 - Perfluorocarbon resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 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 less than.../federal_register/code_of_federal_regulations/ibr_locations.html. The melt viscosity of the...

  9. VOLUMETRIC POLYMERIZATION SHRINKAGE OF CONTEMPORARY COMPOSITE RESINS

    PubMed Central

    Nagem, Halim; Nagem, Haline Drumond; Francisconi, Paulo Afonso Silveira; Franco, Eduardo Batista; Mondelli, Rafael Francisco Lia; Coutinho, Kennedy Queiroz

    2007-01-01

    The polymerization shrinkage of composite resins may affect negatively the clinical outcome of the restoration. Extensive research has been carried out to develop new formulations of composite resins in order to provide good handling characteristics and some dimensional stability during polymerization. The purpose of this study was to analyze, in vitro, the magnitude of the volumetric polymerization shrinkage of 7 contemporary composite resins (Definite, Suprafill, SureFil, Filtek Z250, Fill Magic, Alert, and Solitaire) to determine whether there are differences among these materials. The tests were conducted with precision of 0.1 mg. The volumetric shrinkage was measured by hydrostatic weighing before and after polymerization and calculated by known mathematical equations. One-way ANOVA (á=0.05) was used to determine statistically significant differences in volumetric shrinkage among the tested composite resins. Suprafill (1.87±0.01) and Definite (1.89±0.01) shrank significantly less than the other composite resins. SureFil (2.01±0.06), Filtek Z250 (1.99±0.03), and Fill Magic (2.02±0.02) presented intermediate levels of polymerization shrinkage. Alert and Solitaire presented the highest degree of polymerization shrinkage. Knowing the polymerization shrinkage rates of the commercially available composite resins, the dentist would be able to choose between using composite resins with lower polymerization shrinkage rates or adopting technical or operational procedures to minimize the adverse effects deriving from resin contraction during light-activation. PMID:19089177

  10. Modified resins for solid-phase extraction

    DOEpatents

    Fritz, James S. (Ames, IA); Sun, Jeffrey J. (Ames, IA)

    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.

  11. Modified resins for solid-phase extraction

    DOEpatents

    Fritz, James S. (Ames, IA); Sun, Jeffrey J. (Ames, IA)

    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.

  12. 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.

  13. 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.

  14. Direct Tensile Strength and Characteristics of Dentin Restored with All-Ceramic, Resin-Composite, and Cast Metal Prostheses Cemented with Resin Adhesives.

    PubMed

    Piemjai, Morakot; Nakabayashi, Nobuo

    2015-01-01

    A dentin-cement-prosthesis complex restored with either all-porcelain, cured resin-composite, or cast base metal alloy and cemented with either of the different resin cements was trimmed into a mini-dumbbell shape for tensile testing. The fractured surfaces and characterization of the dentin-cement interface of bonded specimens were investigated using a Scanning Electron Microscope. A significantly higher tensile strength of all-porcelain (12.5 ± 2.2?MPa) than that of cast metal (9.2 ± 3.5?MPa) restorations was revealed with cohesive failure in the cement and failure at the prosthesis-cement interface in Super-Bond C&B group. No significant difference in tensile strength was found among the types of restorations using the other three cements with adhesive failure on the dentin side and cohesive failure in the cured resin. SEM micrographs demonstrated the consistent hybridized dentin in Super-Bond C&B specimens that could resist degradation when immersed in hydrochloric acid followed by NaOCl solutions whereas a detached and degraded interfacial layer was found for the other cements. The results suggest that when complete hybridization of resin into dentin occurs tensile strength at the dentin-cement is higher than at the cement-prosthesis interfaces. The impermeable hybridized dentin can protect the underlying dentin and pulp from acid demineralization, even if detachment of the prosthesis has occurred. PMID:26539520

  15. Direct Tensile Strength and Characteristics of Dentin Restored with All-Ceramic, Resin-Composite, and Cast Metal Prostheses Cemented with Resin Adhesives

    PubMed Central

    Piemjai, Morakot; Nakabayashi, Nobuo

    2015-01-01

    A dentin-cement-prosthesis complex restored with either all-porcelain, cured resin-composite, or cast base metal alloy and cemented with either of the different resin cements was trimmed into a mini-dumbbell shape for tensile testing. The fractured surfaces and characterization of the dentin-cement interface of bonded specimens were investigated using a Scanning Electron Microscope. A significantly higher tensile strength of all-porcelain (12.5 ± 2.2?MPa) than that of cast metal (9.2 ± 3.5?MPa) restorations was revealed with cohesive failure in the cement and failure at the prosthesis-cement interface in Super-Bond C&B group. No significant difference in tensile strength was found among the types of restorations using the other three cements with adhesive failure on the dentin side and cohesive failure in the cured resin. SEM micrographs demonstrated the consistent hybridized dentin in Super-Bond C&B specimens that could resist degradation when immersed in hydrochloric acid followed by NaOCl solutions whereas a detached and degraded interfacial layer was found for the other cements. The results suggest that when complete hybridization of resin into dentin occurs tensile strength at the dentin-cement is higher than at the cement-prosthesis interfaces. The impermeable hybridized dentin can protect the underlying dentin and pulp from acid demineralization, even if detachment of the prosthesis has occurred. PMID:26539520

  16. 21 CFR 172.862 - Oleic acid derived from tall oil fatty acids.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...register/code_of_federal_regulations/ibr_locations.html. (2) The resin acid content does not exceed 0.01 as...register/code_of_federal_regulations/ibr_locations.html. (3) The requirements for absence of chick-edema...

  17. A medicated polycarboxylate cement to prevent complications in composite resin therapy

    SciTech Connect

    Okamoto, Y.; Shintani, H.; Yamaki, M. )

    1990-01-01

    Preparative treatment is the preferred method to protect the dentin and pulp from complications in composite resin therapy. This study investigated the in vivo effects of the polycarboxylate cement containing zinc fluoride and tannic acid in composite resin restorations. Scanning electron micrographs established that the composite resin failed to contact the axial wall. The gaps varied from 10 to 60 microns. However, this polycarboxylate cement was shown to provide excellent adaptation to dentin when used as a base and its chemical adhesion allowed it to make close contact with the unetched dentin. The newly developed electron probe x-ray microanalyzer revealed that the in vivo penetration of fluoride and zinc occurred through the dentinal tubules. When this polycarboxylate cement was used, the orifices of dentinal tubules were partially occluded, possibly with the smear layer fixed by tannic acid. In addition, by releasing the components, this polycarboxylate cement adds acid resistance to dentin and increases the resistance of dentin collagen to proteolytic enzymes. As such this polycarboxylate cement offers advantages as a base to composite resin therapy.

  18. 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.

  19. 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.

  20. Method for selective plugging using resin emulsions

    SciTech Connect

    Friedman, R.H.

    1982-10-05

    Methods and compositions are provided for selectively plugging the water-rich strata of subterranean formations, including injection into the formation of a water-insoluble, oil-soluble resin emulsion. A series of chemical reactions is initiated insitu such that the emulsion demulsifies, resulting in the coalescence of resin droplets. The coalesced water-insoluble, oil-soluble resin droplets are effective to selectively plug the water-rich strata over a relatively long distance and over a relatively long period of time.

  1. 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).

  2. Accurate determination of ?¹Ca concentrations in spent resins from the nuclear industry by accelerator mass spectrometry.

    PubMed

    Nottoli, Emmanuelle; Bourlès, Didier; Bienvenu, Philippe; Labet, Alexandre; Arnold, Maurice; Bertaux, Maité

    2013-12-01

    The radiological characterisation of nuclear waste is essential for managing storage sites. Determining the concentration of Long-Lived RadioNuclides (LLRN) is fundamental for their long-term management. This paper focuses on the measurement of low (41)Ca concentrations in ions exchange resins used for primary fluid purification in Pressurised Water Reactors (PWR). (41)Ca concentrations were successfully measured by Accelerator Mass Spectrometry (AMS) after the acid digestion of resin samples, followed by radioactive decontamination and isobaric suppression through successive hydroxide, carbonate, nitrate and final CaF2 precipitations. Measured (41)Ca concentrations ranged from 0.02 to 0.03 ng/g, i.e. from 0.06 to 0.09 Bq/g. The (41)Ca/(60)Co activity ratios obtained were remarkably reproducible and in good agreement with the current ratio used for resins management. PMID:24144617

  3. Effects of solvent on solution prepregging of the resin system LaRC{trademark}-IAX-2

    SciTech Connect

    Cano, R.J.; Massey, C.P.; St. Clair, T.L.

    1996-12-31

    This work assesses the feasibility of using an alternative solvent for the production of composites from polyimide resin systems via solution prepregging. Previous work on solution prepregging of polyimide systems at NASA Langley Research Center has concentrated on the use of the solvent N-methylpyrrolidinone. An alternative solvent with a similar boiling point, -{gamma}-Butyrolactone, was used to prepare the poly(amide acid) version of LaRC{trademark}-IAX-2. These solutions were subsequently used to prepare prepreg and graphite-reinforced composites. Mechanical properties are presented for the resin system LaRC{trademark}-IAX-2 (4% and 5% offset in stoichiometry and endcapped with phthalic anhydride) impregnated onto Hercules IM7 carbon fiber. Results from this work were compared to data obtained on the same resin system which had been solution prepregged with the solvent N-methylpyrrolidinone.

  4. Controlled methyl-esterification of pectin catalyzed by cation exchange resin.

    PubMed

    Peng, Xiaoxia; Yang, Guang; Fan, Xingchen; Bai, Yeming; Ren, Xiaomeng; Zhou, Yifa

    2016-02-10

    This study developed a new method to methyl-esterify pectin using a cation exchange resin. Homogalacturonan (HG)-type pectin (WGPA-3-HG) and rhamnogalacturonan (RG)-I-type pectin (AHP-RG) obtained from the roots of Panax ginseng and sunflower heads, respectively, were used as models. Compared to commonly used methyl-esterification methods that use either methyl iodide or acidified methanol, the developed method can methyl-esterify both HG- and RG-I-type pectins without degrading their structures via ?-elimination or acid hydrolysis. In addition, by modifying reaction conditions, including the mass ratio of resin to pectin, reaction time, and temperature, the degree of esterification can be controlled. Moreover, the resin and methanol can be recycled to conserve resources, lower costs, and reduce environmental pollution. This new methodology will be highly useful for industrial esterification of pectin. PMID:26686175

  5. 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.

  6. Microleakage at the resin-alloy interface of chemically retained composite resins for cast restorations.

    PubMed

    Strygler, H; Nicholls, J I; Townsend, J D

    1991-06-01

    New retentive mechanisms between veneering resins and casting alloys are claimed to have a chemical bond that results in a high bond strength combined with low microleakage between the veneering resin and cast restoration. This study compared the microleakage of four chemical bonding mechanisms when three veneering resins were bonded to two dental casting alloys. Resin-veneered alloy disks were immersed in red India ink and kept at 37 degrees C for 72 hours. The disks were then bench dried for 24 hours. The resin veneer was sectioned into eight sectors in an engineering milling machine and these resin sectors were removed to display the microleakage pattern. It was concluded that (1) no microleakage was found in two combinations, and (2) the highest microleakage was with Sr-Isosit-N/Panavia EX/Firmilay combinations. PMID:1712849

  7. Sorption of beryllium from fluorine-containing solutions by amino-phosphonate amphoteric ion-exchange resins

    SciTech Connect

    Pakholkov, V.S.; Rychkov, V.N.

    1981-10-20

    Sorption of beryllium ions by a series of amino-phosphonate amphoteric ion-exchange resins from BeF/sub 2/ solutions containing HF, NH/sub 4/F.HF, and NH/sub 4/F has been studied. The influence of the salt form of the resin, concentration of fluoride ions, and beryllium content in the original solutions was demonstrated. The mechanism of ion exchange on amphoteric ion-exchangers was postulated on the basis of chemical analysis and sorption and IR-spectroscopic data. Conclusions are drawn regarding the participation of phosphorus-containing groups of the resins in exchange. Data are presented on desorption of complex fluoride ions and beryllium from amphoteric ion-exchange resins by solutions of hydrofluoric, hydrochloric, and sulfuric acids, ammonium fluoride, and ammonium hydrogenfluoride.

  8. The Bond Strength of Resin Bonded Bridge Retainers to Abutments of Differing Proportions of Enamel and Composite.

    PubMed

    Durey, Kathryn; Nattress, Brian

    2015-03-01

    Four groups of specimens were constructed using bovine enamel and composite resin. After a period of ageing, the specimens were roughened and acid etched before they were cemented to air abraded base metal alloy beams with a universal resin cement. After further ageing, tensile peel testing was carried out using a Universal Testing Machine. The force required to produce failure increased as the amount of composite resin on the bonding surface of the abutment increased. This difference reached statistical significance (p < 0.5) when the abutments contained > 50% composite. The mode of failure was mixed on the majority of retainers. Within the limitations of the study, findings suggest that RBB retainers can be cemented to abutments restored with composite resin without a reduction in bond strength. PMID:26415336

  9. Simultaneous production of high quality biodiesel and glycerin from Jatropha oil using ion-exchange resins as catalysts and adsorbent.

    PubMed

    Shibasaki-Kitakawa, Naomi; Kanagawa, Keiichi; Nakashima, Kazunori; Yonemoto, Toshikuni

    2013-08-01

    The simultaneous production of high quality biodiesel and glycerin was realized by a bench-scale process using expanded-bed reactors packed with cation- and anion-exchange resins. The mixed-solution of crude Jatropha oil and methanol at a stoichiometric molar ratio was supplied to the process. The free fatty acid as well as triglyceride was completely converted to biodiesel. All by-products were adsorbed on the resin and the effluent from the process was free from them. The effluent fully met the international biodiesel standard specifications without any downstream purification processes except for removing methanol. The glycerin adsorbed on the resin was completely recovered as a transparent methanol solution during regeneration of the resin. PMID:23796424

  10. 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 the oxygenated simulant into the feed tank. The dissolved oxygen (DO) concentration of the recirculating simulant was monitored, and the amount of oxygen that reacted with the resin was determined from the change in the DO concentration of the recirculating simulant solution. Prior to hydraulic testing the resin for runs 2 and 3 was covered with the simulant solution and irradiated in a spent fuel element at the Oak Ridge National Laboratory High Flux Isotope Reactor (HFIR). Both batches of resin were irradiated to a total gamma dose of 177 Mrad, but the resin for run 2 reached a maximum temperature during irradiation of 51 C, while the resin for run 3 reached a temperature of 38 C. The different temperatures were the result of the operating status of HFIR at the time of the irradiation and were not part of the test plan; however, the results clearly show the impact of the higher-temperature exposure during irradiation. The flow rate and pressure drop data from the test loop runs show that irradiating the RF resin reduces both the void fraction and the permeability of the resin bed. The mechanism for the reduction in permeability is not clear because irradiation increases the particle size of the resin beads and makes them deform less under pressure. Microscopic examination of the resin beads shows that they are all smooth regular spheres and that irradiation or oxygen uptake did not change the shape of the beads. The resin reacts rapidly with DO in the simulant solution, and the reaction with oxygen reduces the permeability of a bed of new resin by about 10% but has less impact on the permeability of irradiated resin. Irradiation increases the toughness of the resin beads, probably by initiating cross-linking reactions in them. Oxygen uptake reduces the crush strength of both new and irradiated resin; however, the pressures that caused the beads to crush are much higher than would be expected during the operation of an ion exchange column. There was no visible evidence of broken beads in any of the resin samples taken from the test loop. Reaction with oxygen red

  11. Separation and determination of arsenic species in water by selective exchange and hybrid resins.

    PubMed

    Ben Issa, Nureddin; Rajakovi?-Ognjanovi?, Vladana N; Marinkovi?, Aleksandar D; Rajakovi?, Ljubinka V

    2011-11-01

    A simple and efficient method for separation and determination of inorganic arsenic (iAs) and organic arsenic (oAs) in drinking, natural and wastewater was developed. If arsenic is present in water prevailing forms are inorganic acids of As(III) and As(V). oAs can be found in traces as monomethylarsenic acid, MMA(V), and dimethylarsenic acid, DMAs(V). Three types of resins: a strong base anion exchange (SBAE) and two hybrid (HY) resins: HY-Fe and HY-AgCl, based on the activity of hydrated iron oxides and a silver chloride were investigated. It was found that the sorption processes (ion exchange, adsorption and chemisorptions) of arsenic species on SBAE (ion exchange) and HY resins depend on pH values of water. The quantitative separation of molecular and ionic forms of iAs and oAs was achieved by SBAE and pH adjustment, the molecular form of As(III) that exists in the water at pH <8.0 was not bonded with SBAE, which was convenient for direct determination of As(III) concentration in the effluent. HY-Fe resin retained all arsenic species except DMAs(V), which makes possible direct measurements of this specie in the effluent. HY-AgCl resin retained all iAs which was convenient for direct determination of oAs species concentration in the effluent. The selective bonding of arsenic species on three types of resins makes possible the development of the procedure for measuring and calculation of all arsenic species in water. In order to determine capacity of resins the preliminary investigations were performed in batch system and fixed bed flow system. Resin capacities were calculated according to breakthrough points in a fixed bed flow system which is the first step in designing of solid phase extraction (SPE) module for arsenic speciation separation and determination. Arsenic adsorption behavior in the presence of impurities showed tolerance with the respect to potential interference of anionic compounds commonly found in natural water. Proposed method was established performing standard procedures: with external standard, certified reference material and standard addition method. Two analytical techniques: the inductively coupled plasma mass spectrometry (ICP-MS) and atomic absorption spectroscopy-hydride generation (AAS-GH) were comparatively applied for the determination of arsenic in all arsenic species in water. ICP-MS detection limit was 0.2 ?g L(-1) and relative standard deviation (RSD) of all arsenic species investigated was between 3.5 and 5.1%. PMID:21995928

  12. Three new pentasaccharide resin glycosides from the roots of sweet potato (Ipomoea batatas).

    PubMed

    Yin, Yong-Qin; Huang, Xue-Feng; Kong, Ling-Yi; Niwa, Masatake

    2008-12-01

    Three new pentasaccharide resin glycosides, batatosides III-V (1-3), were isolated from the roots of Sweet potato (Ipomoea batatas). Saponification of the crude resin glycoside mixture yielded substituents and simonic acid B. The structures of the isolated compounds (1-3) were established through spectroscopic analyses, including high field NMR spectroscopy and HR-ESI-MS, and chemical correlation. The major characteristics of 3 are the presence of three different substituents, especially the substituent of cinnamic acid was seldom. The monosaccharides of 1-3 were proved by GC-MS and the absolute configuration of aglycone was further established as S by Mosher's method with R-methyloxyphenylacetic acid (MPA) and S-MPA. PMID:19043237

  13. Method for regenerating magnetic polyamine-epichlorohydrin resin

    DOEpatents

    Kochen, Robert L. (Boulder, CO); Navratil, James D. (Simi Valley, CA)

    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.

  14. 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.

  15. Phosphorus recovery as struvite from eutropic waters by XDA-7 resin.

    PubMed

    Li, Huanwen; Ye, Zhiping; Lin, Ying; Wang, Fengying

    2012-01-01

    Phosphorus releases into aquatic environment and its subsequent contribution to eutrophication have resulted in a widespread global pollution issue. However, phosphorus is a non-renewable source. The potential supplies of phosphorus are decreasing worldwide. Therefore, removal and recovery of phosphorus from the eutropic waters is important, emergent and necessary. In this research, experiments for recovering phosphate from eutropic waters by anion exchange combined with struvite precipitation were conducted. The results indicated that the prepared XDA-7 resin was an effective adsorbent for phosphate. The adsorption isotherm of XDA-7 resin was found to be a modified Freundlich type. The maximum phosphate adsorption (20.9 mg/g) occurred in the pH range of 6.0-8.0. Phosphate adsorbed on the XDA-7 resin was effectively desorbed with 8% NaCl solution, and the resin was able to be regenerated with 3% NaClO and 4% NaOH solutions. Phosphate desorbed from the resin was recovered as magnesium ammonium phosphate (struvite). The obtained struvite was analyzed by acid dissolution method, scanning electron microscope (SEM) and Fourier transform infrared spectroscopy (FTIR). The struvite precipitate was found to be 75.8% in purity, a high-value fertilizer. PMID:22643401

  16. Use of ion exchange resins in the analysis of rocks and minerals: Separation of sodium and potassium

    USGS Publications Warehouse

    Reichen, L.E.

    1958-01-01

    This procedure was developed primarily for analyses in which limited amounts of sample are available. Sodium and potassium can be separated from the other constituents of silicate rocks by cation exchange resin (Amberlite IR-120). The sample is decomposed with hydrofluoric and sulfuric acids and passed through the resin bed after expulsion of the fluorine. The column is eluted with 0.12N hydrochloric acid at a fast flow rate of 4 ml. per sq. cm. per minute and the sodium and potassium are recovered together within a reasonable time. Other constituents of the sample, except silica, can be determined on the same portion of sample.

  17. Resin Flow Analysis in the Injection Cycle of a Resin Transfer Molded Radome

    NASA Astrophysics Data System (ADS)

    Golestanian, Hossein; Poursina, Mehrdad

    2007-04-01

    Resin flow analysis in the injection cycle of an RTM process was investigated. Fiberglass and carbon fiber mats were used as reinforcements with EPON 826 epoxy resin. Numerical models were developed in ANSYS finite element software to simulate resin flow behavior into a mold of conical shape. Resin flow into the woven fiber mats is modeled as flow through porous media. The injection time for fiberglass/epoxy composite is found to be 4407 seconds. Required injection time for the carbon/epoxy composite is 27022 seconds. Higher injection time for carbon/epoxy part is due to lower permeability value of the carbon fibers compared to glass fiber mat.

  18. 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.

  19. Effects of Porous Polystyrene Resin Parameters on Candida antarctica Lipase B Adsorption, Distribution, and Polyester Synthesis Activity

    SciTech Connect

    Chen,B.; Miller, M.; Gross, R.

    2007-01-01

    Polystyrene resins with varied particle sizes (35 to 350-600 {mu}m) and pore diameters (300-1000 {angstrom}) were employed to study the effects of immobilization resin particle size and pore diameter on Candida antarctica Lipase B (CALB) loading, distribution within resins, fraction of active sites, and catalytic properties for polyester synthesis. CALB adsorbed rapidly (saturation time {<=}4 min) for particle sizes 120 {mu}m (pore size = 300 {angstrom}). Infrared microspectroscopy showed that CALB forms protein loading fronts regardless of resin particle size at similar enzyme loadings ({approx}8%). From the IR images, the fractions of total surface area available to the enzyme are 21, 33, 35, 37, and 88% for particle sizes 350-600, 120, 75, 35 {mu}m (pore size 300 {angstrom}), and 35 {mu}m (pore size 1000 {angstrom}), respectively. Titration with methyl p-nitrophenyl n-hexylphosphate (MNPHP) showed that the fraction of active CALB molecules adsorbed onto resins was {approx}60%. The fraction of active CALB molecules was invariable as a function of resin particle and pore size. At {approx}8% (w/w) CALB loading, by increasing the immobilization support pore diameter from 300 to 1000 {angstrom}, the turnover frequency (TOF) of {var_epsilon}-caprolactone ({var_epsilon}-CL) to polyester increased from 12.4 to 28.2 s{sup -1}. However, the {var_epsilon}-CL conversion rate was not influenced by changes in resin particle size. Similar trends were observed for condensation polymerizations between 1,8-octanediol and adipic acid. The results herein are compared to those obtained with a similar series of methyl methacrylate resins, where variations in particle size largely affected CALB distribution within resins and catalyst activity for polyester synthesis.

  20. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...hydrocarbons obtainable from sulfate turpentine and meeting the following specifications: Drop-softening point of 118°-138 °C; iodine value less than 20. (b) Terpene resins consisting of polymers of beta-pinene and meeting the following...

  1. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...hydrocarbons obtainable from sulfate turpentine and meeting the following specifications: Drop-softening point of 118°-138 °C; iodine value less than 20. (b) Terpene resins consisting of polymers of beta-pinene and meeting the following...

  2. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... components of polypropylene film intended for use in contact with food, and the terpene resins identified in paragraph (b) of this section may be safely used as components of polyolefin film intended for use...

  3. 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.

  4. 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.

  5. 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.

  6. 21 CFR 177.1585 - Polyestercarbonate resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...locations.html. (ii) A minimum weight-average molecular weight of 27,000, as determined by gel permeation chromatography using polystyrene standards. (2) Extractives limitations. The polyestercarbonate resins to be tested shall be...

  7. 21 CFR 177.1585 - Polyestercarbonate resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...locations.html. (ii) A minimum weight-average molecular weight of 27,000, as determined by gel permeation chromatography using polystyrene standards. (2) Extractives limitations. The polyestercarbonate resins to be tested shall be...

  8. Cesium-specific phenolic ion exchange resin

    DOEpatents

    Bibler, Jane P. (Aiken, SC); Wallace, Richard M. (Aiken, SC)

    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.

  9. 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.

  10. 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... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Nylon resins. 177.1500 Section 177.1500 Food...

  11. 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... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Nylon resins. 177.1500 Section 177.1500 Food...

  12. 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... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Nylon resins. 177.1500 Section 177.1500 Food...

  13. 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..., see the List of CFR Sections Affected, which appears in the Finding Aids section of the printed volume... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Nylon resins. 177.1500 Section 177.1500 Food...

  14. Clinical applications of preheated hybrid resin composite.

    PubMed

    Rickman, L J; Padipatvuthikul, P; Chee, B

    2011-07-01

    This clinical article describes and discusses the use of preheated nanohybrid resin composite for the placement of direct restorations and luting of porcelain laminate veneers. Two clinical cases are presented. Preheating hybrid composite decreases its viscosity and film thickness offering the clinician improved handling. Preheating also facilitates the use of nanohybrid composite as a veneer luting material with relatively low polymerisation shrinkage and coefficient of thermal expansion compared to currently available resin luting cements. PMID:21779058

  15. 40 CFR 414.40 - Applicability; description of the thermoplastic resins subcategory.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...Resins, Compounded *Polyethylene, Chlorinated *Polyimides *Polypropylene Resins Polystyrene (Crystal) Polystyrene (Crystal) Modified *Polystyrene—Copolymers *Polystyrene—Acrylic Latexes Polystyrene Impact Resins...

  16. 40 CFR 414.40 - Applicability; description of the thermoplastic resins subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...Resins, Compounded *Polyethylene, Chlorinated *Polyimides *Polypropylene Resins Polystyrene (Crystal) Polystyrene (Crystal) Modified *Polystyrene—Copolymers *Polystyrene—Acrylic Latexes Polystyrene Impact Resins...

  17. 40 CFR 414.40 - Applicability; description of the thermoplastic resins subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...Resins, Compounded *Polyethylene, Chlorinated *Polyimides *Polypropylene Resins Polystyrene (Crystal) Polystyrene (Crystal) Modified *Polystyrene—Copolymers *Polystyrene—Acrylic Latexes Polystyrene Impact Resins...

  18. 40 CFR 414.40 - Applicability; description of the thermoplastic resins subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...Resins, Compounded *Polyethylene, Chlorinated *Polyimides *Polypropylene Resins Polystyrene (Crystal) Polystyrene (Crystal) Modified *Polystyrene—Copolymers *Polystyrene—Acrylic Latexes Polystyrene Impact Resins...

  19. 40 CFR 414.40 - Applicability; description of the thermoplastic resins subcategory.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...Resins, Compounded *Polyethylene, Chlorinated *Polyimides *Polypropylene Resins Polystyrene (Crystal) Polystyrene (Crystal) Modified *Polystyrene—Copolymers *Polystyrene—Acrylic Latexes Polystyrene Impact Resins...

  20. Influence of contamination on resin bond strength to nano-structured alumina-coated zirconia ceramic.

    PubMed

    Zhang, Shanchuan; Kocjan, Andraz; Lehmann, Frank; Kosmac, Tomaz; Kern, Matthias

    2010-08-01

    The purpose of this study was to evaluate the influence of contamination and subsequent cleaning on the bond strength and durability of an adhesive resin to nano-structured alumina-coated zirconia ceramic. Zirconia ceramic disks were coated with nano-structured alumina, utilizing the hydrolysis of aluminum nitride powder. After immersion in saliva or the use of a silicone disclosing agent, specimens were cleaned with phosphoric acid etching or with tap water rinsing only. Uncontaminated specimens served as controls. Plexiglas tubes filled with composite resin were bonded with a phosphate monomer [10-methacryloxydecyl-dihydrogenphosphate (MDP)]-containing resin (Panavia 21). Subgroups of eight specimens each were stored in distilled water at 37 degrees C, either for 3 d without thermal cycling (TC) or for 150 d with 37,500 thermal cycles from 5 to 55 degrees C. The tensile bond strength (TBS) was determined using a universal testing machine at a crosshead speed of 2 mm min(-1). The topography of the debonded surface was scrutinized for fractographic features, utilizing both optical and scanning electron microscopy. The TBS to uncontaminated nano-structured alumina-coated zirconia ceramic was durable, while contamination significantly reduced the TBS. Phosphoric acid cleaning was effective in removal of saliva contamination from the coated bonding surface but was not effective in removal of the silicone disclosing agent. Nano-structured alumina coating improves resin bonding to zirconia ceramic and eliminates the need for air-abrasion before bonding. PMID:20662914

  1. Composite Properties of Polyimide Resins Made From "Salt-Like" Solution Precursors

    NASA Technical Reports Server (NTRS)

    Cano, Roberto J.; Weiser, Erik S.; SaintClair, Terry L.; Echigo, Yoshiaki; Kaneshiro, Hisayasu

    1997-01-01

    Recent work in high temperature materials at NASA Langley Research Center (LaRC (trademark)) have led to the development of new polyimide resin systems with very attractive properties. The majority of the work done with these resin systems has concentrated on determining engineering mechanical properties of composites prepared from a poly(amide acid) precursor. Three NASA Langley-developed polyimide matrix resins, LaRC (trademark) -IA, LaRC (trademark) -IAX, and LaRC (trademark) -8515, were produced via a salt-like process developed by Unitika Ltd. The 'salt-like' solutions (sixty-five percent solids in NMP) were prepregged onto Hexcel IM7 carbon fiber using the NASA LaRC Multipurpose Tape Machine. Process parameters were determined and composite panels fabricated. Mechanical properties are presented for these three intermediate modulus carbon fiber/polyimide matrix composites and compared to existing data on the same polyimide resin systems and IM7 carbon fiber manufactured via poly(amide acid) solutions (thirty-five percent solids in NMP). This work studies the effects of varying the synthetic route on the processing and mechanical properties of polyimide composites.

  2. Glycine feeding improves pristinamycin production during fermentation including resin for in situ separation.

    PubMed

    Zhang, Li-Jing; Jin, Zhi-Hua; Chen, Xiao-Guang; Jin, Qin-Chao; Feng, Ming-Guang

    2012-05-01

    Seven amino acids were tested as precursors to affect pristinamycin production by a mutant strain derived from Streptomyces pristinaespiralis ATCC25486. Of those, glycine was selected as the best precursor to facilitate both cell growth and pristinamycin production at the feeding time of 36-h incubation and the feeding rate of 0.75 g L(-1) flask culture. The optimized time and concentration of glycine feeding were applied to enlarged 3-L bioreactor fermentation with a resin added at the time of 20-h fermentation for in situ separation. As a result, a combination of the glycine feeding and the added resin resulted in the maximal pristinamycin yield of 616 mg L(-1) culture 12 h after glycine feeding. The yield from the combined treatment was 1.71-, 2.77- and 4.32-fold of those from the mere glycine and resin treatments and the control, respectively. Other parameters, including intracellular nucleic acid content, animo nitrogen content and pH level, during 72-h fermentation were also given in association with the pristinamycin yields in the different treatments. The results indicate that glycine feeding is an effective approach to enhance pristinamycin production in the culture of S. pristinaespiralis F213 with supplemented resin for in situ separation. PMID:21947672

  3. Qualification of Reillex{trademark} HPQ anion exchange resin for use in SRS processes

    SciTech Connect

    Crooks, W.J. III

    2000-05-18

    The Phase 2 portion of the HB-Line facility was built in the early 1980's to process plutonium and neptunium from nitric acid solutions into oxide suitable for storage in a vault. Although the other portions of HB-Line were started up in the mid 1980's and have operated since that time, the anion exchange and precipitation processes in Phase 2 were never started up. As part of the material stabilization efforts, Phase 2 is currently being started up. A new anion exchange resin is needed because the resins that were proposed for use 10 years ago are limited by performance characteristics, disposal requirements, or are no longer commercially available. SRTC is responsible for qualifying all resins prior to their use in Nuclear Materials Stabilization and Storage (NMSS) processes. Qualification consists of both process suitability and thermal stability with nitric acid. This report describes the thermal stability qualification of Reillex{trademark} HPQ, the new resin proposed for processing plutonium and neptunium in the HB Line facility.

  4. Effect of simulated resin-bonded fixed partial denture clinical conditions on resin cement mechanical properties.

    PubMed

    Walker, M P; Spencer, P; Eick, J D

    2003-08-01

    The purpose of this study was to determine changes in flexural properties of resin cement under simulated resin-bonded fixed partial denture (RBFPD) clinical conditions using aqueous ageing and cyclic loading. Panavia F flexural modulus and strength were measured by static loading to failure after 48-h and 60-day aqueous ageing at 37 degrees C with and without simulated cyclic occlusal loading. Panavia F sorption and solubility were also measured. Scanning electron microscopy (SEM) was used to characterize the morphology of the fractured surfaces. A two-factor anova (P resin matrix fracture occurred in static-aqueous specimens; while in the aqueous-cycled specimens, resin matrix fracture occurred in addition to an increasing proportion of filler/resin interface fracture. Collectively, these outcomes suggest that initial degradation under simulated resin cement clinical function may be related to breakdown of the filler/resin interface bond, which could contribute to in vivo RBFPD resin cement cohesive failure. PMID:12880409

  5. Colesevelam and colestipol: novel medication resins in the gastrointestinal tract.

    PubMed

    Arnold, Michael A; Swanson, Benjamin J; Crowder, Clinton D; Frankel, Wendy L; Lam-Himlin, Dora; Singhi, Aatur D; Stanich, Peter P; Arnold, Christina A

    2014-11-01

    We report the morphologic description of the bile acid sequestrants (BAS) colesevelam and colestipol, as well as the largest series of cholestyramine. Histologically similar medication resins from 4 institutions were prospectively collected over 1 year (26 specimens, 15 patients). Comorbidities included hyperlipidemia (4/15), hypertension (4/15), inflammatory bowel disease (4/15), coronary artery disease (3/15), diarrhea (7/15), hypothyroidism (2/15), and ischemic bowel (1/15). Sites of involvement included the esophagus (1/26), stomach (1/26), small intestine (1/26), ileocecal valve (1/26), and colorectum (22/26). Associated histologic diagnoses included normal (8/26), chronic mucosal injury (11/26), acute inflammation (9/26), erosion/ulceration (6/26), and cytomegalovirus (2/26). The BAS resins were histologically indistinguishable from each other; they were all eosinophilic on hematoxylin and eosin (H&E) and lacked internal "fish-scales." To validate these observations, respective medications were submitted for histologic processing; the processed medications were identical to those in the patient specimens. Rare, irregular "fracture" lines presented diagnostic pitfalls by mimicking the true "fish-scales" of Kayexalate and sevelamer. Clues to the correct identification of BAS include recognition that the "fracture" lines were subtle, irregular, and restricted to large fragments or thick sections, likely representing a processing artifact. Moreover, Kayexalate is violet on H&E and black on acid fast bacillus, and sevelamer characteristically displays a 2-tone color on H&E and is magenta on acid fast bacillus. An association with inflammatory injury was seen (15/26). We believe that the BAS are innocent bystanders in complicated patients, although we cannot exclude their ability to cause mucosal injury in specific settings. PMID:24921636

  6. PETIs as High-Temperature Resin-Transfer-Molding Materials

    NASA Technical Reports Server (NTRS)

    Connell, John N.; Smith, Joseph G., Jr.; Hergenrother, Paul M.

    2005-01-01

    Compositions of, and processes for fabricating, high-temperature composite materials from phenylethynyl-terminated imide (PETI) oligomers by resin-transfer molding (RTM) and resin infusion have been developed. Composites having a combination of excellent mechanical properties and long-term high-temperature stability have been readily fabricated. These materials are particularly useful for the fabrication of high-temperature structures for jet-engine components, structural components on highspeed aircraft, spacecraft, and missiles. Phenylethynyl-terminated amide acid oligomers that are precursors of PETI oligomers are easily made through the reaction of a mixture of aromatic diamines with aromatic dianhydrides at high stoichiometric offsets and 4-phenylethynylphthalic anhydride (PEPA) as an end-capper in a polar solvent such as N-methylpyrrolidinone (NMP). These oligomers are subsequently cyclodehydrated -- for example, by heating the solution in the presence of toluene to remove the water by azeotropic distillation to form low-molecular-weight imide oligomers. More precisely, what is obtained is a mixture of PETI oligomeric species, spanning a range of molecular weights, that exhibits a stable melt viscosity of less than approximately 60 poise (and generally less than 10 poise) at a temperature below 300 deg C. After curing of the oligomers at a temperature of 371 deg C, the resulting polymer can have a glass-transition temperature (Tg) as high as 375 C, the exact value depending on the compositions.

  7. 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.

  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 unsuccessfully attacked or wounded trees to resist future bark beetle attacks. Forest management that encourages healthy, vigorously growing trees will also favor larger resin ducts, thereby conferring increased constitutive resistance to bark beetle attacks. PMID:26433021

  9. Physiological activities of hydroxyl fatty acids

    Technology Transfer Automated Retrieval System (TEKTRAN)

    In the search of value-added products from surplus soybean oil, we produced many new hydroxy fatty acids through microbial bioconversion. Hydroxy fatty acids are used in a wide range of industrial products, such as resins, waxes, nylons plastics, lubricants, cosmetics, and additives in coatings and...

  10. Uptake of metal ions by a new chelating ion exchange resin. Part 3: Protonation constants via potentiometric titration and solid state [sup 31]P NMR spectroscopy

    SciTech Connect

    Nash, K.L.; Rickert, P.G.; Muntean, J.V.; Alexandratos, S.D.

    1994-01-01

    A new chelating ion exchange resin which incorporates methylenediphosphonate, carboxylate, and sulfonate functional groups in a polystyrene-divinylbenzene matrix has been prepared. This resin exhibits exceptionally high affinity for polyvalent cations even from moderately acidic aqueous media. Metal ion coordination occurs primarily at the diphosphonate group with the secondary binding sites contributing to charge neutralization when necessary and possible, and to increasing hydrophilicity of the resin pores. In the present investigation, the protonation equilibria of the phosphonate groups in the resin are investigated via potentiometric titration and solid-state [sup 31]P NMR spectroscopy of the resin. Intrinsic equilibrium constants for the first two diphosphonate protonation reactions are pK[sub 4] = 10.47 and pK[sub 3] = 7.24. The last two protons added to the diphosphonate group are acidic having pK[sub a] values less than 2.5. These protonation constants are consistent with those reported previously for monomer analog 1,1-diphosphonic acids. This result implies that thermodynamic data available in the literature can be used to predict the relative affinity of the resin for polyvalent cations. 17 refs., 2 figs., 3 tabs.

  11. Anomalous effects in the character of the carbonyl absorption (ca. 1700 cm/sup -1/) in the infrared spectra of petroleum resins and asphaltenes

    SciTech Connect

    Speight, J.G.; Moschopedis, S.E.

    1981-09-01

    The presence of the carbonyl functional groups in asphaltenes and resins were detected by ir spectroscopy following saponification. By following the spectra through a reaction sequence, the bituminous extracts from fresh oil sands showed the presence of esters and carboxylic acids. The extracts from a hot water process showed either carboxylic acids or esters. 1 figure, 2 tables.

  12. Studies on cesium uptake by phenolic resins

    SciTech Connect

    Samanta, S.K.; Ramaswamy, M.; Misra, B.M. )

    1992-02-01

    The selective removal of cesium by phenolic ion-exchange resins from highly salted alkaline radioactive solutions was studied. The resins were synthesized by alkaline polycondensation of phenol, resorcinol, catechol, and resorcinol-catechol mixture with formaldehyde and characterized for their moisture regain, ion-exchange (H{sup +} {yields} Na{sup +}) capacity, and distribution coefficient (K{sub D}) for cesium. The effects of open and sealed curing of the polymers on their properties were studied. The effect of Na{sup +}, NaOH, and Cs{sup +} concentration on the uptake of cesium by resorcinol-formaldehyde resin was investigated, in particular. The chemical, thermal, and radiation stabilities of the polymers were also studied.

  13. Airway responsiveness in workers processing polyester resins.

    PubMed

    Zuskin, E; Saric, M; Bouhuys, A

    1979-12-01

    In 22 employees of a button-manufacturing plant, exposure to polyester resins over an eight-hour work shift resulted in an acute reduction of flow rates on maximum expiratory flow volume (MEFV) curves at MEF50% and MEF25%. In the workers studied, preshift administration of 80 mg of propranolol potentiated, while 1 mg of subcutaneously injected atropine significantly inhibited, the bronchoconstricting effect of the resins, indicating that the autonomic nervous system plays an important role in determining airway smooth muscle response to polyester resins. Although a high prevalence of acute symptoms (cough, shortness of breath, throat and eye irritation) over the work shift was recorded in exposed workers, no high prevalence of chronic respiratory symptoms was found. No definite evidence of chronic airway obstruction was recorded in exposed workers. PMID:536858

  14. Corrosion of resin-bonded orthodontic brackets.

    PubMed

    Gwinnett, A J

    1982-06-01

    The objective was to identify the nature and origin of indelible black and green stains found in enamel after the removal of bonded orthodontic brackets. Several brackets were examined by scanning electron microscopy and energy-dispersive x-ray analysis. Irrespective of the type of bracket or resin, morphologic evidence of corrosion activity was found. Brackets were pitted, and in some cases large amounts of metal were missing. Cracks were found in the resin which led to sites of destruction in which structures resembling microorganisms were also found. X-ray analysis showed the presence of chromium, nickel, iron, and chlorine in significant amounts in the bonding, discolored resin. It was concluded that the cracks were favoring crevice corrosion. In the presence of organisms and a lowered pH, together with a chloride environment and an oxygen gradient, conditions conducive to corrosion are established. PMID:6758601

  15. 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.

  16. 21 CFR 177.1650 - Polysulfide polymer-polyepoxy resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... soybean oil Epoxy resins (as listed in § 175.300(b)(3)(viii)(a) of this chapter). Ethylene glycol... sample of the finished resin in the form in which it contacts food, when subjected to ASTM method...

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

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3300 Hydrophilic resin coating for dentures. (a) Identification. A hydrophilic resin...

  18. 21 CFR 872.3820 - Root canal filling resin.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3820 Root canal filling resin. (a) Identification. A root canal filling resin is a...

  19. 21 CFR 872.3820 - Root canal filling resin.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3820 Root canal filling resin. (a) Identification. A root canal filling resin is a...

  20. 21 CFR 872.3200 - Resin tooth bonding agent.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3200 Resin tooth bonding agent. (a) Identification. A resin tooth bonding agent is a...

  1. 21 CFR 872.3300 - Hydrophilic resin coating for dentures.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3300 Hydrophilic resin coating for dentures. (a) Identification. A hydrophilic resin...

  2. 21 CFR 872.3820 - Root canal filling resin.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3820 Root canal filling resin. (a) Identification. A root canal filling resin is a...

  3. 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.

  4. 21 CFR 173.25 - Ion-exchange resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...cubic foot per minute; or (B) Extracts of the resin will be found to contain...3-Dimethylaminopropylamine in Food Simulating Extracts of Ion Exchange Resins,” February...for the isolation and purification of protein concentrates and isolates under the...

  5. 21 CFR 173.25 - Ion-exchange resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...cubic foot per minute; or (B) Extracts of the resin will be found to contain...3-Dimethylaminopropylamine in Food Simulating Extracts of Ion Exchange Resins,” February...for the isolation and purification of protein concentrates and isolates under the...

  6. 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.

  7. 21 CFR 177.1650 - Polysulfide polymer-polyepoxy resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 2013-04-01 false Polysulfide polymer-polyepoxy resins. 177.1650 Section...CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components...Surfaces § 177.1650 Polysulfide polymer-polyepoxy resins....

  8. 21 CFR 177.1650 - Polysulfide polymer-polyepoxy resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 2012-04-01 false Polysulfide polymer-polyepoxy resins. 177.1650 Section...CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components...Surfaces § 177.1650 Polysulfide polymer-polyepoxy resins....

  9. 21 CFR 177.1650 - Polysulfide polymer-polyepoxy resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 2014-04-01 false Polysulfide polymer-polyepoxy resins. 177.1650 Section...CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components...Surfaces § 177.1650 Polysulfide polymer-polyepoxy resins....

  10. 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.

  11. 21 CFR 173.40 - Molecular sieve resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...resin (expressed in terms of water regain), and a particle size...thoroughly washed with potable water prior to their first use in...resins are used as the gel filtration media in the final purification of partially delactosed...

  12. 21 CFR 872.3770 - Temporary crown and bridge resin.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...3770 Temporary crown and bridge resin. (a) Identification. A temporary crown and bridge resin is a device composed of a material, such as polymethylmethacrylate...prosthesis, such as a crown or bridge, for use until a...

  13. 21 CFR 872.3770 - Temporary crown and bridge resin.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...3770 Temporary crown and bridge resin. (a) Identification. A temporary crown and bridge resin is a device composed of a material, such as polymethylmethacrylate...prosthesis, such as a crown or bridge, for use until a...

  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. 21 CFR 177.2490 - Polyphenylene sulfide resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...Polyphenylene sulfide resins consist of basic resins produced by the reaction of equimolar parts of p- dichlorobenzene and sodium sulfide...following specifications as determined by methods titled “Oxygen Flask Combustion-Gravimetric Method for Determination...

  16. ACC Resin Statistics Annual Summary PRODUCTION, SALES & CAPTIVE USE

    E-print Network

    Laughlin, Robert B.

    .1 (1) Except Phenolic resins, which are reported on a gross weight basis. (2) Sales & Captive Use dataACC Resin Statistics Annual Summary PRODUCTION, SALES & CAPTIVE USE (millions of pounds, dry weight

  17. 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.

  18. Biphenyl liquid crystalline epoxy resin as a low-shrinkage resin-based dental restorative nanocomposite.

    PubMed

    Hsu, Sheng-Hao; Chen, Rung-Shu; Chang, Yuan-Ling; Chen, Min-Huey; Cheng, Kuo-Chung; Su, Wei-Fang

    2012-11-01

    Low-shrinkage resin-based photocurable liquid crystalline epoxy nanocomposite has been investigated with regard to its application as a dental restoration material. The nanocomposite consists of an organic matrix and an inorganic reinforcing filler. The organic matrix is made of liquid crystalline biphenyl epoxy resin (BP), an epoxy resin consisting of cyclohexylmethyl-3,4-epoxycyclohexanecarboxylate (ECH), the photoinitiator 4-octylphenyl phenyliodonium hexafluoroantimonate and the photosensitizer champhorquinone. The inorganic filler is silica nanoparticles (?70-100 nm). The nanoparticles were modified by an epoxy silane of ?-glycidoxypropyltrimethoxysilane to be compatible with the organic matrix and to chemically bond with the organic matrix after photo curing. By incorporating the BP liquid crystalline (LC) epoxy resin into conventional ECH epoxy resin, the nanocomposite has improved hardness, flexural modulus, water absorption and coefficient of thermal expansion. Although the incorporation of silica filler may dilute the reinforcing effect of crystalline BP, a high silica filler content (?42 vol.%) was found to increase the physical and chemical properties of the nanocomposite due to the formation of unique microstructures. The microstructure of nanoparticle embedded layers was observed in the nanocomposite using scanning and transmission electron microscopy. This unique microstructure indicates that the crystalline BP and nanoparticles support each other and result in outstanding mechanical properties. The crystalline BP in the LC epoxy resin-based nanocomposite was partially melted during exothermic photopolymerization, and the resin expanded via an order-to-disorder transition. Thus, the post-gelation shrinkage of the LC epoxy resin-based nanocomposite is greatly reduced, ?50.6% less than in commercialized methacrylate resin-based composites. This LC epoxy nanocomposite demonstrates good physical and chemical properties and good biocompatibility, comparable to commercialized composites. The results indicate that this novel LC nanocomposite is worthy of development and has potential for further applications in clinical dentistry. PMID:22842038

  19. Amino resins crosslinked polymer gels for permeability profile control

    SciTech Connect

    Shu, P.

    1989-05-30

    This patent describes a process for closing pores in a hydrocarbonaceous fluid bearing formation to obtain improved sweep efficiency during a waterflood oil recovery operation which comprises injecting a gellable composition comprising: (a) water; (b) 0.2 to 5.0 wt. percent of a cross linkable polymer which is a member selected from the group consisting of xanthan biopolymers, heteropolysaccharide S-130, poly (acrylamide-co-acrylamido-2-methyl-propanesulfonate), and acrylamide modified polyvinyl alcohol; and (c) 0.02 to 50.0 wt. percent of a partially methylated aminoplast resin which cross links with the polymer thereby forming a gel in the absence of a salt which is acid generating upon the application of heat which gel is of a strength sufficient to close pores in one or more permeable zones of the formation.

  20. Chromate (CrO(4)(2-)) and copper (Cu2+) adsorption by dual-functional ion exchange resins made from agricultural by-products.

    PubMed

    Marshall, Wayne E; Wartelle, Lynda H

    2006-07-01

    Ion exchange resins commonly have a single functionality for either cations or anions. Resins that have a dual functionality for both cations and anions are uncommon. The objective of this study was to create dual-functional ion exchange resins derived from soybean hulls, sugarcane bagasse and corn stover. Dual-functional resins were prepared by two separate two-step processes. In the first two-step process, by-products were reacted with a solution of citric acid in order to impart additional negative charge, and then reacted with the cross-linking reagent dimethyloldihydroxyethylene urea (DMDHEU) and a quaternary amine (choline chloride) to add positive charge to the lignocellulosic material. In the second two-step process, the order of reaction was reversed, with positive charge added first, followed by the addition of negative charge. These combined reactions added both cationic and anionic character to the by-products as evidenced by the increased removal from solution of copper (Cu(2+)) cation and the chromate (CrO(4)(2-)) anion compared to unmodified by-products. The order of reaction appeared to slightly favor the functionality that was added last. That is, if negative charge was added last, the resulting resin sequestered more copper ion than a comparable resin where the negative charge was added first and vice-versa. Cu(2+) and CrO(4)(2-) were used as marker ions in a solution that contained both competing cations and anions. The dual-functional resins adsorbed as much as or more of the marker ions compared to commercial cation or anion exchange resins used for comparison. None of the commercial resins exhibited dual-functional properties to the same extent as the by-product-based resins. PMID:16764901

  1. Technology development for phosphoric acid fuel cell powerplant (phase 2)

    NASA Technical Reports Server (NTRS)

    Christner, L.

    1979-01-01

    The status of technology for the manufacturing and testing of 1200 sq. cm cell materials, components, and stacks for on-site integrated energy systems is assessed. Topics covered include: (1) preparation of thin layers of silicon carbide; (2) definition and control schemes for volume changes in phosphoric acid fuel cells; (3) preparation of low resin content graphite phenolic resin composites; (4) chemical corrosion of graphite-phenolic resin composites in hot phosphoric acid; (5) analysis of electrical resistance of composite materials for fuel cells; and (6) fuel cell performance and testing.

  2. In vitro wear of resin-based materials--simultaneous corrosive and abrasive wear.

    PubMed

    Correr, Gisele Maria; Bruschi Alonso, Roberta Caroline; Correr Sobrinho, Lourenço; Puppin-Rontani, Regina Maria; Ferracane, Jack Liborio

    2006-07-01

    The aim of this study was to evaluate the wear of resin-based materials caused by the association of abrasive and corrosive processes. Twenty specimens were prepared for each material, cast in epoxy in acrylic rings, polished, and profiled with an MTS 3D Profiler. Antagonists were made from deciduous molars. Specimens were distributed into eight groups (n = 10), according to the material (Filtek Supreme, Point 4, Dyract AP, and Fuji II LC) and the type of slurry (neutral and acidic), and then cycled 100,000 times in the OHSU oral wear simulator. The specimens were cleaned and reprofiled. Volume loss and maximum depth were determined. ANOVA and Tukey's test were used for data analysis (p < 0.05). The area of the wear facet on the antagonist was also measured. Composites displayed less wear than the compomer and the resin-modified glass ionomer. Significant differences also were found for cusp wear, with a significant positive correlation shown between cusp and material wear. The acidic slurry significantly increased the wear of the materials compared to the neutral slurry. Exposure to acidic slurry accelerated the wear of resin-based materials. PMID:16292764

  3. 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.

  4. 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.

  5. Thermal analysis of bismaleimide matrix resins

    SciTech Connect

    Spieker, D.A.

    1990-07-01

    Commercial bismaleimide (BMI) resins for composite applications have mechanical properties with values between those of high temperature epoxies and fully aromatic polyimides. The former have the disadvantage of poor hot-wet strength and the latter have the disadvantages of being difficult to process and costly. Current commercial BMI formulations offer good properties retention under hot/wet conditions, comparative ease of processing, and moderate cost. We have used thermal analysis extensively to study commercial BMI materials. This paper will survey the results to TGA, TMA, and DMA analyses which were performed to characterize the thermal behavior of cured BMI resins. 3 refs., 6 figs.

  6. Characterization of the resin transfer moulding process

    NASA Astrophysics Data System (ADS)

    Kendall, K. N.; Rudd, C. D.; Owen, M. J.; Middleton, V.

    1992-12-01

    Complete process characterization is required to enable high volume manufacture of composite components by resin transfer moulding (RTM). A review of processing literature indicates adequate understanding of the thermal cycle but limited understanding of the pressure cycle. Experimental results are presented to characterize both the thermal and pressure cycles during RTM, verifying published findings in instances and developing them in others. A phase of post-impregnation cavity pressure is identified which is considered to be caused by thermal expansion of liquid resin adjacent to the gate. Results are presented to demonstrate that this pressure phase can be more significant than impregnation pressure when considering mould design.

  7. 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.

  8. 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.

  9. 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

  10. Chelating resin immobilizing carboxymethylated polyethyleneimine for selective solid-phase extraction of trace elements: Effect of the molecular weight of polyethyleneimine and its carboxymethylation rate.

    PubMed

    Kagaya, Shigehiro; Kajiwara, Takehiro; Gemmei-Ide, Makoto; Kamichatani, Waka; Inoue, Yoshinori

    2016-01-15

    The effect of the molecular weight of polyethyleneimine (PEI), defined as a compound having two or more ethyleneamine units, and of its carboxymethylation rate (CM/N), represented by the ratio of ion-exchange capacity to the amount of N on the resin, on the selective solid-phase extraction ability of the chelating resin immobilizing carboxymethylated (CM) PEI was investigated. The chelating resins (24 types) were prepared by immobilization of diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, PEI300 (MW=ca. 300), and PEI600 (MW=ca. 600) on methacrylate resins, followed by carboxymethylation with various amounts of sodium monochloroacetate. When resins with approximately the same CM/N ratio (0.242-0.271) were used, the recovery of Cd, Co, Cu, Fe, Ni, Pb, Ti, Zn, and alkaline earth elements increased with increasing the molecular weight of PEIs under acidic and weakly acidic conditions; however, the extraction behavior of Mo and V was only slightly affected. This was probably due to the increase in N content of the resin, resulting in an increase in carboxylic acid groups; the difference in the molecular weight of PEIs immobilized on the resin exerts an insignificant influence on the selective extraction ability. The CM/N ratio considerably affected the extraction behavior for various elements. Under acidic and neutral conditions, the recovery of Cd, Co, Cu, Fe, Ni, Pb, Ti, and Zn increased with increasing CM/N values. However, under these conditions, the recovery of alkaline earth elements was considerably low when a resin with low CM/N ratio was used. This is presumably attributed to the different stability constants of the complexes of these elements with aminocarboxylic acids and amines, and to the electrostatic repulsion between the elements and the protonated amino groups in the CM-PEI. The recovery of Mo and V decreased or varied with increasing CM/N values, suggesting that the extraction of these elements occurred mainly by the anion-exchange reaction. For the separation and preconcentration of trace elements in samples containing large amounts of alkali and alkaline earth elements, the CM-PEI600 resin with CM/N=0.131 (Cu(II) extraction capacity, 0.37mmolg(-)(1)) was found to be the most suitable because it scarcely extracts alkali and alkaline earth elements under acidic and neutral conditions. This resin proved to be convenient for separating and preconcentrating Cd, Co, Cu, Fe, Mn, Mo, Ni, Pb, V, and Zn in the certified reference materials (EnviroMAT EU-L-1 wastewater and ES-L-1 ground water) and commercially available table salt. PMID:26592617

  11. 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)...

  12. 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)...

  13. 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)...

  14. 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)...

  15. 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)...

  16. 40 CFR 721.3135 - Phosphorous modified epoxy resin (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Phosphorous modified epoxy resin... Specific Chemical Substances § 721.3135 Phosphorous modified epoxy resin (generic). (a) Chemical substance... phosphorous modified epoxy resin (PMNs P-00-992 and P-01-471) is subject to reporting under this section...

  17. 40 CFR 721.2755 - Cycloaliphatic epoxy resin (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Cycloaliphatic epoxy resin (generic... Substances § 721.2755 Cycloaliphatic epoxy resin (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as cycloaliphatic epoxy resin...

  18. 40 CFR 721.2752 - Epoxy resin containing phosphorus (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 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...

  19. 40 CFR 721.3135 - Phosphorous modified epoxy resin (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Phosphorous modified epoxy resin... Specific Chemical Substances § 721.3135 Phosphorous modified epoxy resin (generic). (a) Chemical substance... phosphorous modified epoxy resin (PMNs P-00-992 and P-01-471) is subject to reporting under this section...

  20. 40 CFR 721.2755 - Cycloaliphatic epoxy resin (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Cycloaliphatic epoxy resin (generic... Substances § 721.2755 Cycloaliphatic epoxy resin (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as cycloaliphatic epoxy resin...

  1. 49 CFR 173.165 - Polyester resin kits.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ...2011-10-01 2011-10-01 false Polyester resin kits. 173.165 Section...Class 1 and Class 7 § 173.165 Polyester resin kits. (a) Except for transportation by aircraft, polyester resin kits consisting of a base...

  2. 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...

  3. 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...

  4. 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...

  5. 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...

  6. 21 CFR 177.2410 - Phenolic 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 Phenolic resins in molded articles. 177.2410... as Components of Articles Intended for Repeated Use § 177.2410 Phenolic resins in molded articles. Phenolic resins identified in this section may be safely used as the food-contact surface of...

  7. 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...

  8. 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.

  9. 21 CFR 872.3200 - Resin tooth bonding agent.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...2010-04-01 2010-04-01 false Resin tooth bonding agent. 872.3200 Section 872.3200...Prosthetic Devices § 872.3200 Resin tooth bonding agent. (a) Identification. A resin tooth bonding agent is a device material, such...

  10. 21 CFR 872.3200 - Resin tooth bonding agent.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...2011-04-01 2011-04-01 false Resin tooth bonding agent. 872.3200 Section 872.3200...Prosthetic Devices § 872.3200 Resin tooth bonding agent. (a) Identification. A resin tooth bonding agent is a device material, such...

  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 177.2410 - Phenolic resins in molded articles.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Phenolic resins in molded articles. 177.2410... (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use Only as Components of Articles Intended for Repeated Use § 177.2410 Phenolic resins in molded articles. Phenolic resins identified in this section...

  13. Effects of resin addition on holographic polymer dispersed liquid crystals

    NASA Astrophysics Data System (ADS)

    Vita, F.; Lucchetta, D. E.; Castagna, R.; Criante, L.; Simoni, F.

    2009-02-01

    The effects of epoxy resin addition to a standard acrylate-based holographic polymer dispersed liquid-crystal mixture are investigated. Different resin concentrations are used and we show how the presence of the resin results in transmission gratings characterized by negligible scattering, polarization independent behaviour and lower switching voltages. These experimental results are explained by means of morphological scanning electron microscopy analyses.

  14. 76 FR 39896 - Granular Polytetrafluoroethylene Resin From Italy

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-07

    ... Granular Polytetrafluoroethylene Resin From Italy Determination On the basis of the record \\1\\ developed in... antidumping duty order on granular polytetrafluoroethylene resin from Italy would be likely to lead to... Granular Polytetrafluoroethylene Resin from Italy: Investigation No. 731-TA-385 (Third Review). By order...

  15. 75 FR 67105 - Granular Polytetrafluoroethylene Resin From Italy and Japan

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-11-01

    ... granular polytetrafluoroethylene resin from Italy (53 FR 33163). Following first five-year reviews by... duty orders on imports of granular polytetrafluoroethylene resin from Italy and Japan (65 FR 6147... polytetrafluoroethylene resin from Italy and Japan (70 FR 76026). The ] Commission is now conducting third reviews...

  16. 49 CFR 173.165 - Polyester resin kits.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 2013-10-01 2013-10-01 false Polyester resin kits. 173.165 Section 173.165...Other Than Class 1 and Class 7 § 173.165 Polyester resin kits. (a) Polyester resin kits consisting of a base material...

  17. 49 CFR 173.165 - Polyester resin kits.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ...2012-10-01 2012-10-01 false Polyester resin kits. 173.165 Section...Class 1 and Class 7 § 173.165 Polyester resin kits. (a) Except for transportation by aircraft, polyester resin kits consisting of a base...

  18. 49 CFR 173.165 - Polyester resin kits.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 2014-10-01 2014-10-01 false Polyester resin kits. 173.165 Section 173.165...Other Than Class 1 and Class 7 § 173.165 Polyester resin kits. (a) Polyester resin kits consisting of a base material...

  19. 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...

  20. 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...

  1. 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...

  2. 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...

  3. 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...

  4. 21 CFR 872.3670 - Resin impression tray material.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...Identification. Resin impression tray material is a device intended for...device consists of a resin material, such as methyl methacrylate...the fabrication of crowns, bridges, or full dentures. A preliminary...The resin impression tray material is applied to this...

  5. 21 CFR 872.3670 - Resin impression tray material.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...Identification. Resin impression tray material is a device intended for...device consists of a resin material, such as methyl methacrylate...the fabrication of crowns, bridges, or full dentures. A preliminary...The resin impression tray material is applied to this...

  6. 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...

  7. 40 CFR 721.5905 - Modified phenolic resin (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 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...

  8. 40 CFR 721.5905 - Modified phenolic resin (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 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...

  9. 40 CFR 721.5905 - Modified phenolic resin (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 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...

  10. 40 CFR 721.5908 - Modified phenolic resin (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 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...

  11. 40 CFR 721.5908 - Modified phenolic resin (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 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...

  12. 40 CFR 721.5908 - Modified phenolic resin (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 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...

  13. 40 CFR 721.5908 - Modified phenolic resin (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 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...

  14. 40 CFR 721.5905 - Modified phenolic resin (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 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...

  15. 40 CFR 721.5762 - Aromatic aldehyde phenolic resin (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 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...

  16. 40 CFR 721.5762 - Aromatic aldehyde phenolic resin (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 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...

  17. 40 CFR 721.5762 - Aromatic aldehyde phenolic resin (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 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...

  18. 40 CFR 721.5762 - Aromatic aldehyde phenolic resin (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 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...

  19. On the Fatigue Behavior of Resin-Dentin Bonds after Degradation by Biofilm

    PubMed Central

    Mutluay, Mustafa Murat; Zhang, Ke; Ryou, Heonjune; Yahyazadefar, Mobin; Majd, Hessam; Xu, Hockin H. K.; Arola, Dwayne

    2012-01-01

    The durability of resin-dentin bonds is a growing concern in the placement of composite restorations. Most reported evaluations concerning the mechanical behavior of the bonded interface are conducted using static loading to failure only. They also do not account for the acid production of biofilms, which is one of the most common contributors to interfacial failures in vivo. In this investigation resin-dentin bonded interface specimens were exposed to S. mutans for 14 days and then subjected to quasi-static or cyclic four-point flexure to failure. Control specimens (without biofilm) were evaluated after aging for one and fourteen days. While no significant difference in flexure strength resulted from the duration of water aging (66.2 MPa vs 56.9 MPa), biofilm exposure caused a significant reduction in strength (29.3 MPa; p?0.000). After water aging for one and fourteen days the apparent endurance limits were 13.0 MPa and 13.1 MPa, respectively. Biofilm treatment caused a significant (p?0.001) reduction in fatigue resistance of the interface, and the endurance limit was reduced to 9.9 MPa. Fatigue failure of the control specimens initiated within the resin composite adjacent to the interface, whereas failure of the biofilm treated specimens initiated within the hybrid layer and appeared attributed to the localized demineralization of dentin. Biofilm degradation is an important consideration in assessing the durability of resin-dentin bonds. PMID:23276517

  20. Effects of sports beverages and polishing systems on color stability of different resin composites

    PubMed Central

    Ta?k?nsel, Ertan; Özel, Emre; Öztürk, Elif

    2014-01-01

    Background: Consumption of certain acidic beverages may alter the physical and esthetic properties of resin composites. Aim: The aim of this study was to evaluate the effects of two sports beverages on color stability of two different types of resin composites polished with different composite polishing systems. Materials and Methods: A total of 96 disk-shaped specimens (diameter: 8-mm and thickness: 2-mm) were made from two different resin composites (Cavex Quadrant Universal-LC, and Clearfil-APX). All of the specimens were stored in distilled water for 24 h at 37°C. Color measurements of each specimen were performed using a colorimeter according to the CIEL*a*b* color scale at baseline and after seven days of immersion in two different sports beverages (Powerade and Buzzer). Statistical Analysis Used: The data were evaluated using Kruskal Wallis and Mann-Whitney U tests. Results: Significant differences were found between the mean ?E values of the groups after seven days of immersion (P < 0.05). The highest level of the mean color change was observed in the Clearfil APX specimens immersed in Powerade (?E = 3.5 ± 0.9). Control groups stored in distilled water for both composites exhibited small color changes (?E-Cavex-bur = 2.1 ± 1; ?E-Clearfil APX-bur = 2.1 ± 0.4). Conclusion: Sport beverages caused discoloration in the resin composites after seven days. PMID:25125843