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Sample records for r-btp extraction resins

  1. Extraction chromatography of neodymium by an organophosphorous extractant supported on various polymeric resins

    SciTech Connect

    Takigawa, D.Y.

    1993-04-01

    Fifteen resins coated with dihexyl-N,N-diethylcarbamoylmethyl phosphonate (CMP) were studied for their extraction of neodymium (Nd) in 4.0 and 7.0 M nitric acid. Resin properties, such as chemical composition and physical morphology, which can influence Nd extraction as well as subsequent resin regeneration (Nd stripping), were identified. Hydrophilic or polar resins coated with CMP efficiently extracted the Nd. Resins initially washed free of residual monomer and solvent before CMP coating outperformed their untreated counterparts. The macroporous styrene-divinylbenzene hydrophobic resins that were high in surface area were less effective supports compared with hydrophilic microporous Aurorez, polybenzimidazole (PBI) and macroporous Amberlite polyacrylic resins. Only one resin, Duolite C-467, showed no measurable improvement in Nd extraction with CMP coating. CMP-coated Aurorez PBI, a microporous and hydrophilic polymeric resin with an average surface area, showed the best overall efficiency for Nd removal and resin regeneration.

  2. Modified resins for solid-phase extraction

    DOEpatents

    Fritz, James S.; Sun, Jeffrey J.

    1991-12-10

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

  3. Modified resins for solid-phase extraction

    DOEpatents

    Fritz, James S.; Sun, Jeffrey J.

    1993-07-27

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

  4. Ultrasonic extraction of resins from an historic textile.

    PubMed

    Rezi?, I; Krsti?, D; Boki?, Lj

    2008-01-01

    Ultrasound assisted extraction was applied on the historical textile as the most appropriate sample preparation step for the identification of the resinous binder. Fragile silk banner from the 19th century was analyzed for the presence of different resins. After the ultrasonic extraction with ethyl acetate in the ultrasonic bath, resinous materials and unknown sample from the banner were separated by thin layer chromatography. The multiple developments in benzene-methanol (95:5) system as mobile phase and silica gel layer as stationary phase were applied, and afterwards the video densitometry determination of the components was performed by means of video camera HV-C20. The shellac resin was determined as an important part of the complex binder. PMID:17822938

  5. DIFFERENTIATION OF FOUR NORTHERN GREAT PLAINS SOILS USING RESIN EXTRACTION

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Because resin extraction of soils has revealed sensitivities of plants to the extractable V:(V+P) and Mg:(Mg +Ca) molar ratios, we examined the Barnes and Buse soils in the northern Great Plains of North Dakota, South Dakota and Minnesota. Because of their close association with Svea and Langhei soi...

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

    NASA Astrophysics Data System (ADS)

    Sano, Yuichi; Surugaya, Naoki; Yamamoto, Masahiko

    2010-03-01

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

  7. Fatty and resinic acids extractions from crude tall oil

    SciTech Connect

    Nogueira, J.M.F.

    1996-11-01

    The separation of fatty and resinic acidic fractions from crude tall-oil soap solutions with n-heptane by the technique of dissociation extraction is discussed. The theory of the overall process is supported by a systematic study developed to cover the high selectivity demonstrated in the differential solubility and the aptness between fatty and diterpenic acids to both liquids phases. To study the main factors affecting those liquid-liquid extraction systems and the amphiphilic behavior of such molecules involved, sodium salts aqueous solutions of crude tall oil and synthetic mixtures as molecular acidic models were used.

  8. In vitro color change of three dental veneering resins in tea, coffee and tamarind extracts

    PubMed Central

    Subramanya, J.K.; Muttagi, S.

    2011-01-01

    Objective To study the in vitro color changes of three dental resin veneering materials when immersed in tea, coffee and tamarind extracts. Materials and Methods The color changes of heat polymerized tooth colored acrylic resin (Stellondetrey, B, F14, DPI Dental products of India Ltd, Mumbai), auto polymerized tooth colored acrylic resin (DPI, B, QV5, DPI Dental products of India Ltd, Mumbai) and light polymerized resin composite (Herculite XRV, Enamel A2, part no. 22860, lot no. 910437, Kerr Corporation, West Collins Avenue, Orange, CA, USA) when immersed in water extracts of tea (Tata Tea Ltd. Bangalore, India), coffee (Tata Coffee Ltd. Coorg, India) and tamarind were evaluated using computer vision systems. The color images were recorded in R (red), G (green) and B (blue) form and converted into H (hue), S (saturation) and V (value). Results Significant color change occurred for auto polymerized tooth colored acrylic resin in tamarind extract, for heat polymerized tooth colored acrylic resin in tea extract and for light polymerized resin composite in coffee extract. Auto polymerized tooth colored acrylic resin samples showed an overall higher color change. However, for all the material samples coffee extract produced more color change. Conclusion These results suggest that the color stability of the resins is influenced by the presence of secondary metabolites such as tartaric acid, tannins, caffeine, saponins and phenols in tamarind, tea and coffee extracts. PMID:22457841

  9. Fermium purification using TEVA{trademark} resin extraction chromatography

    SciTech Connect

    Porter, C.E.; Riley, F.D. Jr.; Vandergrift, R.D.; Felker, L.K.

    1997-01-01

    The Radiochemical Engineering Development Center at Oak Ridge National Laboratory processes irradiated targets to recover the transplutonium actinides for research and industrial users. In a typical processing campaign, dekagram quantities of curium are recovered for recycle into targets for subsequent irradiation and processing; decigram quantities of californium are recovered for fabrication into neutron sources; and milligram quantities of einsteinium and berkelium as well as picogram quantities of fermium are recovered for distribution to the research community. The transcurium actinides are separated in a series of chromatographic elutions using a cation-exchange resin and ammonium {alpha}-hydroxyisobutyrate as the eluant. The fermium fraction from these final purification runs still contains significant amounts of rare earth fission products, such as yttrium, dysprosium, and holmium. In the most recent campaign, a process using a TEVA{trademark} resin extraction chromatography column was developed and tested to determine its effectiveness in providing a fermium product free of rare earth fission products. Gamma spectroscopy indicated that dysprosium and holmium were reduced to levels less than minimum detectable limits and that only 0.07 pg of {sup 91}Y remained in the final fermium product, which contained 0.5 pg of {sup 257}Fm. An overall decontamination factor of {approximately}10{sup 3} was achieved for fission product removal.

  10. Enrichment and separation of chlorogenic acid from the extract of Eupatorium adenophorum Spreng by macroporous resin.

    PubMed

    Liu, Boyan; Dong, Beitao; Yuan, Xiaofan; Kuang, Qirong; Zhao, Qingsheng; Yang, Mei; Liu, Jie; Zhao, Bing

    2016-01-01

    A simple and efficient chromatographic method for separation of chlorogenic acid from Eupatorium adenophorum Spreng extract was developed. The adsorption properties of nine macroporous resins were evaluated. NKA-II resin showed much better adsorption/desorption properties. The adsorption of chlorogenic acid on NKA-II resin at 25°C was well fitted to Langmuir isotherm model and pseudo-second-order kinetic model. The dynamic adsorption and desorption experiments were carried out on columns packed with NKA-II resin to optimize the separation process. The content of chlorogenic acid in the product increased to 22.17%, with a recovery yield of 82.41%. PMID:26625338

  11. 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 (η5-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.

  12. Copolymer resins made of agricultural and forest residues extracts for wood laminating adhesives

    SciTech Connect

    Chen, C.M.

    1995-11-01

    Extracts of Southern pine bark, peanut hulls, pecan nut pitch, and pecan shell flour were used to synthesize copolymer resins using resorcinol, phenol, and formaldehyde. The test joints of both southern pine and oak were laminated in room temperature. The gluability of these copolymer resins were evaluated with shear compression loading test. The effects of resorcinol level, the molar ratio of formaldehyde to phenolic, and the composition of the hardener on bonding quality were investigated. With a more than 80% wood failure after vacuum pressure treatment, several copolymer resins provided good bonding quality as a wood laminating adhesive. Different extracts required different formulations of copolymer resin and hardner to obtain the best bonding quality.

  13. Purification of baicalin and wogonoside from Scutellaria baicalensis extracts by macroporous resin adsorption chromatography.

    PubMed

    Du, Zhanquan; Wang, Kun; Tao, Yuan; Chen, Lixia; Qiu, Feng

    2012-11-01

    In this study, resin adsorption as a means to separate and purify baicalin and wogonoside from extracts of Scutellaria baicalensis was investigated. Among the ten tested resins, the non-polar resin HPD-100 offered the best adsorption and desorption properties. Langmuir and Freundlich isotherms were used to describe the interactions between solutes and resin at different temperatures, and the equilibrium experimental data were well fitted to the two isotherms. Column packed with HPD-100 resin was used to perform dynamic adsorption and desorption tests to optimize the separation process. After one round treatment with HPD-100 resin, the contents of baicalin and wogonoside were 3.6-fold and 12.0-fold increased with recovery yields of 85.7% and 65.6%, respectively. In addition, a laboratory preparative-scale separation was carried out under the final conditions. The results showed that the preparative separation of baicalin and wogonoside can be easily and efficiently achieved via adsorption and desorption on HPD-100 resin. The developed method is a promising basis for large-scale preparation of baicalin and wogonoside from S. baicalensis extracts. PMID:23040984

  14. [Mechanism of gold solid extraction from aurocyanide solution using D3520 resin impregnated with TRPO].

    PubMed

    Yang, Xiang-Jun; Wang, Shi-Xiong; Zou, An-Qin; Chen, Jing; Guo, Hong

    2014-02-01

    Trialkyphosphine oxides (TRPO) was successfully used for the impregnation of D3520 resin to prepare an extractant-impregnated resin (EIR). Solid extraction of Au(I) from alkaline cyanide solution was studied using this extractant-impregnated resin (EIR), with addition of cetyltrimethylammonium bromide (CTMAB), directly into the aurous aqueous phase in advance. The mechanism of solid extraction was further investigated by means of FTIR, XPS and SEM. The column separation studies have shown that cationic surfactant CTMAB played a key role in the solid phase extraction, and the resin containing TRPO were effective for the extraction of gold when the molar ratio of CTMAB: Au( I ) reached 1:1. FTIR spectroscopy of gold loaded EIR showed that the frequency of C[triple bond]N stretching vibration was at 2144 cm(-1), and the frequency of P=O stretching vibration shifted to lower frequency from 1153 to 1150 cm(-1). The XPS spectrum of N(1s), Au(4f7/2) and Au(4f5/2) sugges- ted that the coordination environment of gold did not change before and after extraction, and gold was still as the form of Au (CN)2(-) anion exiting in the loaded resin; O(1s) spectrum showed that the chemically combined water significantly increased after solid extraction from 30.74% to 42.34%; Comparing to the P(2p) spectrum before and after extraction, the binding energy increased from 132. 15 to 132. 45 eV, indicating there maybe existing hydrogen-bond interaction between P=O and water molecule, such as P=O...H-O-H. The above results obtained established that in the solid extraction process, the hydrophobic ion association [CTMA+ x Au(CN)] diffused from the bulk solution into the pores of the EIR, and then be solvated by TRPO adsorbed in the pores through hydrogen bonding bridged by the water molecules. PMID:24822425

  15. 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

  16. Enrichment and purification of madecassoside and asiaticoside from Centella asiatica extracts with macroporous resins.

    PubMed

    Jia, Guangtao; Lu, Xiuyang

    2008-06-01

    In present study, the performance and separation characteristics of five macroporous resins for the enrichment and purification of asiaticoside and madecassoside from Centella asiatica extracts have been evaluated. The adsorption and desorption properties of total triterpene saponins (80% purity) on macroporous resins including HPD100, HPD300, X-5, AB-8 and D101 have been compared. According to our results, HPD100 offered higher adsorption and desorption capacities and higher adsorption speed for asiaticoside and madecassoside than other resins. Column packed with HPD100 resin was used to perform dynamic adsorption and desorption tests to optimize the separation process of asiaticoside and madecassoside from C. asiatica extracts. After the treatment with gradient elution on HPD100 resin, the content of madecassoside in the product increased from 3.9 to 39.7%, and the recovery yield was 70.4%; for asiaticoside the content increased from 2.0 to 21.5%, and the recovery yield was 72.0%. The results showed that HPD100 resin revealed a good ability to separate madecassoside and asiaticoside, and the method can be referenced for the separation of other triterpene saponins from herbal raw materials. PMID:18457845

  17. Separation and recovery of food coloring dyes using aqueous biphasic extraction chromatographic resins.

    PubMed

    Huddleston, J G; Willauer, H D; Boaz, K R; Rogers, R D

    1998-06-26

    Aqueous biphasic systems (ABS) and aqueous biphasic extraction chromatographic (ABEC) resins are currently under investigation for their utility in the removal of color from textile plant wastes. The structures of several widely used food colorings, suggest that these dyes would also be retained on the resins. In work currently in progress, we have begun to investigate the retention and resolution of several common food colorings including indigo carmine, amaranth, carminic acid. erythrosin B, tartrazine and quinoline yellow. The relationship between the uptake of these dyes on ABEC resins in terms of the binding strengths and capacities of the resins and their partitioning behavior in ABS is illustrated. Some possible theoretical and practical approaches to the prediction of the partitioning and retention behavior is discussed. PMID:9699992

  18. Evaluation of extractants and chelating resins in polishing actinide-contaminated waste streams

    SciTech Connect

    Schreiber, S.B.; Dunn, S.L.; Yarbro, S.L.

    1991-06-01

    At the Los Alamos National Laboratory Plutonium Facility, anion exchange is used for recovering plutonium from nitric acid solutions. Although this approach recovers >99%, the trace amounts of plutonium and other actinides remaining in the effluent require additional processing. We are doing research to develop a secondary unit operation that can directly polish the effluent so that actinide levels are reduced to below the maximum allowed for facility discharge. We selected solvent extraction, the only unit operation that can meet the stringent process requirements imposed; several carbonyl and phosphoryl extractants were evaluated and their performance characterized. We also investigated various engineering approaches for solvent extraction; the most promising was a chelating resin loaded with extractant. Our research now focuses on the synthesis of malonamides, and our goal is to bond these extractants to a resin matrix. 7 refs., 12 figs., 1 tab.

  19. [Purification technology of procymidone residues in ginseng extracts by macroporous resins].

    PubMed

    Cui, Li-Li; Zheng, Pei-He; Wang, Ying-Ping

    2014-07-01

    The macroporous resin separation technology has been mainly applied in the enrichment of saponins, flavonoids, alkaloids and other ingredients, and used in the removal of heavy metal impurities and pesticide residues in recent years. This paper focuses on the synthesis of the new-type macroporous adsorption resin LKS-11 according to the molecular structure characteristics of procymidone. Specifically, the selective absorptive property and other advantages of macroporous resin were utilized to analyze the procymidone removal efficiency in ginseng extracts from different sources. The type of macroporous resins, absorptive property and desorption conditions were observed respectively by static and dynamic adsorption methods to determined the optimum process conditions. According to the results, LKS-11 showed a good absorptive property to procymidone in ginseng extracts and provided a theoretical basis for studies on the removal of procymidone residues from ginseng extracts by using macroporous adsorption resin. Because of no secondary pollution on samples, low production and operation costs, high procymidone removal efficiency and high product recovery rate, this method is suitable to be applied in production. PMID:25276973

  20. Chemically modified polymeric resins for high performance liquid chromatography, solid-phase extraction and organic separation by LC and GC

    SciTech Connect

    Sun, Jeffrey Jiafang.

    1991-08-06

    Polystyrene divinylbenzene resins were chemically modified by introduction of various functional groups, which included polar, non-polar, ionic and metallic groups. These chemically modified polymeric resins were used successfully for high performance liquid chromatography, solid phase extraction and some special applications in liquid and gas chromatography. The introduced functional groups offer an additional selectivity parameter for liquid chromatographic separation. The polar derivatized polymeric resins dramatically increased the recoveries of solid phase extraction, especially for polar compounds. The sulfonated polystyrene resins were used for separation of neutral and basic compounds as well as basic and weaker basic compounds. The sulfonated non-porous resin was used amine abstracter and the polymeric-mercuric resin was used as mercaptan abstracter in capillary gas chromatograph. The researches in this dissertation has shown the very promising applications of polystyrene divinylbenzene resin in chromatographic field. 58 refs., 34 figs., 28 tabs.

  1. Effects of Experimental Conditions on Extraction Yield of Extracellular Polymeric Substances by Cation Exchange Resin

    PubMed Central

    Cho, Jinwoo; Hermanowicz, Slawomir W.; Hur, Jin

    2012-01-01

    Effects of experimental conditions on the yield of extracellular polymeric substances (EPSs) extraction by cation exchange resin (CER) were investigated using activated sludge flocs. The experimental variables included resin dose, extraction time, sample dilution, and storage time. An empirical model was proposed to describe the kinetics of extraction process. The extraction yield increases with the extraction time and CER dose until it reached the maximum amount of EPS extraction. The maximum yield of EPS was affected as well by the sample dilution, exhibiting a decreasing trend with increasing dilution factor. It was also found that the amount of EPS extracted from a raw sample depends on the storage time. Once EPS was extracted from the sample, however, the EPS keeps its original quantity under storage at 4C. Based on the model, the maximum amount of EPS extraction and yield rate could be estimated for different conditions. Comparing the model parameters allows one to quantitatively compare the extraction efficiencies under various extracting conditions. Based on the results, we recommend the original sample should be diluted with the volume ratio of above 1?:?2 and a raw sample should be treated quickly to prevent the reduction of sample homogeneity and original integrity. PMID:22919352

  2. Recovery of hesperidin from orange peel by concentration of extracts on styrene-divinylbenzene resin.

    PubMed

    Di Mauro, A; Fallico, B; Passerini, A; Rapisarda, P; Maccarone, E

    1999-10-01

    This paper describes a new procedure for obtaining hesperidin from the waste orange peel of the citrus industry. It is based on the adsorption of dilute extracts of hesperidin on a styrene-divinylbenzene (SDVB) resin and the desorption in much more reduced volumes by means of alkaline eluents. Hesperidin immediately precipitates with good yield and high purity after acidification of the concentrated solutions, thus overcoming disadvantages due to the high dilution. Different experiments were carried out to examine operating conditions in each phase of the process. Hesperidin was extracted from peel with an aqueous saturated Ca(OH)(2) solution, allowing precipitation of calcium pectates from colloidal pectins that can interfere in the subsequent phases of adsorption and separation of hesperidin. The clear extracts were neutralized to optimize adsorption on resin. The most effective eluent was 0.5 N NaOH solution containing 10% ethanol. Recycling of the crystallization liquor improved the yield and purity of the product and reduced the acid amount required for neutralizing fresh alkaline extracts. Resin must be washed after each adsorption-desorption cycle and regenerated after five cycles. Results can constitute a useful starting point for an industrial application. A flow scheme of the process is also reported. PMID:10552823

  3. Determination of weight distribution ratios of Pa(V) and Np(V) with some extraction chromatography resins and the AG1-X8 resin.

    PubMed

    Mendes, M; Aupiais, J; Jutier, C; Pointurier, F

    2013-05-30

    Literature data on distribution ratios (Dw) of Np(V) and Pa(V) for the AG1-X8 resin are scarce whereas those related on resin capacity factors (k') values for TEVA, TRU and U/TEVA resins are absent. Therefore, batch extraction experiments for Pa(V) and Np(V) from HCl and HNO3 media were realized, at tracer scale, with AG1-X8 and EIChroM resins (TEVA, TRU and U/TEVA). Based on the new Dw and k' values obtained in this study, a new protocol for Pa/Np separation has been developed leading to a better separation factor of 10(5) and a chemical yield of 97±3% and 99±1% for Pa and Np, respectively. A separation of (231)Pa from uranium matrix was successfully tested. PMID:23680558

  4. Effect of hexane extract of Boswellia serrata oleo-gum resin on chemically induced liver damage.

    PubMed

    Y, Jyothi; Kamath, Jagadish V; Asad, Mohammed

    2006-04-01

    The hexane extract of oleo-gum-resin of Boswellia serrata (BSHE) was evaluated for its effect on liver injury induced by carbon tetrachloride, paracetamol or thioacetamide. The BSHE was given in two different doses (87.5 mg/kg p.o. and 175 mg/kg p.o.). Silymarin, a known hepatoprotective agent was used as standard. The lower dose of BSHE (87.5 mg/kg p.o.) significantly reduced the elevated levels of serum marker enzymes and prevented the increase in liver weight in all three models of liver injury, while the higher dose showed mild hepatoprotective activity. The hepatoprotective effect of lower dose of BSHE was supported by changes in histopathology. It was concluded that hexane extract of oleo-gum-resin of Boswellia serrata plant in lower doses possess hepatoprotective activity. PMID:16751123

  5. Improved resins and novel materials and methods for solid phase extraction and high performance liquid chromatography

    SciTech Connect

    Freeze, R.

    1997-10-08

    Solid-phase extraction (SPE) has grown to be one of the most widely used methods for isolation and preconcentration of a vast range of compounds from aqueous solutions. By modifying polymeric SPE resins with chelating functional groups, the selective uptake of metals was accomplished. The resin, along with adsorbed metals, was vaporized in the ICP and detection of the metals was then possible using either mass or emission spectroscopy. Drug analyses in biological fluids have received heightened attention as drug testing is on the increase both in sports and in the work environment. By using a direct-injection technique, biological fluids can be injected directly into the liquid chromatographic system with no pretreatment. A new surfactant, a sulfonated form of Brij-30 (Brij-S) is shown to prevent the uptake of serum proteins on commercial HPLC columns by forming a thin coating on the silica C18 surface. Excellent separations of eight or more drugs with a wide range of retention times were obtained. The separations had sharper peaks and lower retention times than similar separations performed with the surfactant sodium dodecylsulfate (SDS). Quantitative recovery of a number of drugs with limits of detection near 1 ppm with a 5 {micro}l injection volume were obtained. Finally, a method for solid-phase extraction in a syringe is introduced. The system greatly reduced the volume of solvent required to elute adsorbed analytes from the SPE bed while providing a semi-automated setup. SPE in a syringe consists of a very small bed of resin-loaded membrane packed into a GC or HPLC syringe. After extraction, elution was performed with just a few {micro}l of solvent. This small elution volume allowed injection of the eluent directly from the syringe into the chromatographic system, eliminating the handling problems associated with such small volumes.

  6. Separation of thorium and uranium from silicate rock samples using two commercial extraction chromatographic resins.

    PubMed

    Yokoyama, T; Makishima, A; Nakamura, E

    1999-01-01

    A new chemical separation technique to isolate Th and U from silicate rocks was established by using two kinds of commercial extraction chromatographic resins. In the first column procedure, with U/TEVA·spec resin, almost all elements except Th and U were eluted by 4 M HNO(3). Th was then separated by using 5 M HCl, and U was finally isolated by successive addition of 0.1 M HNO(3). A significant amount of Zr still remained in the Th fraction, which was then further purified in the second column stage using TEVA·spec resin. In the second procedure, Zr was eluted first by using 2 M HNO(3), and then Th was collected by 0.1 M HNO(3). Both the Th and U fractions obtained by these procedures were sufficiently pure for thermal ionization mass spectrometric (TIMS) analysis. Recovery yields of Th and U exceeded 90%, and total blanks were <19 pg for Th and <10 pg for U. Our method has advantages over previous methods in terms of matrix effects, tailing problems, and degree of isolation. Since Th and U are effectively separated without suffering any matrix interference from coexisting cations and anions, this technique can be used not only for the analysis of igneous rock samples but also for the analysis of soils, marine sediments, carbonates, phosphates and seawater, groundwater, and surface water. PMID:21662935

  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. A novel malonamide grafted polystyrene-divinyl benzene resin for extraction, pre-concentration and separation of actinides.

    PubMed

    Ansari, S A; Mohapatra, P K; Manchanda, V K

    2009-01-30

    A new chelating polymeric extraction chromatographic resin was prepared by chemical anchoring of N,N'-dimethyl-N,N'-dibutyl malonamide (DMDBMA) with chloromethylated Merrifield resin((R)). The grafted resin exhibited stronger binding for hexavalent and tetravalent actinides such as U(VI), Th(IV) and Pu(IV) over trivalent actinides, viz. Am(III) and Pu(III). Batch studies on solid phase extraction performed over a wide range of acid solution (0.01-6M HNO(3)) revealed that ternary mixer of uranium, americium and plutonium or thorium, americium and plutonium could be separated from each other at 1M HNO(3). Desorption of U(VI), Pu(IV) and Am(III) from the loaded resin was efficiently carried out using 0.1M alpha-HIBA, 0.25M oxalic acid and 0.01M EDTA, respectively. Quantitative pre-concentration of actinide ions such as Th(IV) and U(VI) was possible from 3M HNO(3) solution. The practical utility of the grafted resin was evaluated by uranium sorption measurements in several successive cycles. The sorption efficiency of the resin with respect to uranyl ion remained unchanged even after 30 days of continuous use. The surface morphology of the resin was monitored with the help of scanning electron microscopy (SEM) technique. PMID:18541366

  9. Analgesic activity of the ethanolic extract of Shorea robusta resin in experimental animals

    PubMed Central

    Wani, Tariq Ahmad; Kumar, Dhirendra; Prasad, Raju; Verma, Pawan Kumar; Sardar, Kaustuk K.; Tandan, Surendra Kumar; Kumar, Dinesh

    2012-01-01

    Aim: Shorea robusta (Sal), an important traditional Indian medicinal plant used in various ailments and rituals and the indigenous use of the resin of this plant as a medicament for treatment of various inflammatory conditions is well documented in literature. In the present study, ethanolic extract of S. robusta resin (SRE) was evaluated for its analgesic activity by making use of different central and peripheral pain models. Materials and Methods: The analgesic activity of SRE was assessed by employing different pain models such as, i) hot plate and tail flick tests for central analgesia, ii) acetic acid- induced writhing (peripheral analgesic model), iii) formalin-induced hind paw licking (both central and peripheral model), iv) carrageenan-induced hyperalgesia (peripheral analgesic model) and v) post-surgical pain (peripheral analgesic model). Results: The extract produced significant central and peripheral analgesic effects, as is evident from increase in reaction time in hot plate and tail flick tests, inhibition in writhing counts in acetic acid-induced writhing test, inhibition of licking time in formalin-induced hind paw licking, increased pain threshold in paw withdrawal latency in carrageenan-induced hyperalgesia and increased paw withdrawal threshold in post-surgical pain. Conclusion: The results of the present study demonstrate marked antinociceptive effects of SRE. PMID:23087512

  10. Comparison of methods for nutrient measurement in calcareous soils: Ion-exchange resin bag, capsule, membrane, and chemical extractions

    USGS Publications Warehouse

    Sherrod, S.K.; Belnap, J.; Miller, M.E.

    2002-01-01

    Four methods for measuring quantities of 12 plant-available nutrients were compared using three sandy soils in a series of three experiments. Three of the methods use different ion-exchange resin forms-bags, capsules, and membranes-and the fourth was conventional chemical extraction. The first experiment compared nutrient extraction data from a medium of sand saturated with a nutrient solution. The second and third experiments used Nakai and Sheppard series soils from Canyonlands National Park, which are relatively high in soil carbonates. The second experiment compared nutrient extraction data provided by the four methods from soils equilibrated at two temperatures, "warm" and "cold." The third experiment extracted nutrients from the same soils in a field equilibration. Our results show that the four extraction techniques are not comparable. This conclusion is due to differences among the methods in the net quantities of nutrients extracted from equivalent soil volumes, in the proportional representation of nutrients within similar soils and treatments, in the measurement of nutrients that were added in known quantities, and even in the order of nutrients ranked by net abundance. We attribute the disparities in nutrient measurement among the different resin forms to interacting effects of the inherent differences in resin exchange capacity, differences among nutrients in their resin affinities, and possibly the relatively short equilibration time for laboratory trials. One constraint for measuring carbonate-related nutrients in high-carbonate soils is the conventional ammonium acetate extraction method, which we suspect of dissolving fine CaCO3 particles that are more abundant in Nakai series soils, resulting in erroneously high Ca2+ estimates. For study of plant-available nutrients, it is important to identify the nutrients of foremost interest and understand differences in their resin sorption dynamics to determine the most appropriate extraction method.

  11. Characterization of the effects of post-extraction treatments on human dentin-resin interface by micro-Raman spectroscopy

    NASA Astrophysics Data System (ADS)

    Leung, Yiuchong; Morris, Michael D.

    1997-01-01

    Raman microprobe spectroscopy was used to investigate the effects of post-extraction treatments of human dentin on the penetration of the 4-methacryloxyethyl trimellitic acid (4- MET)/methyl methacrylate (MMA)/tri-n-butyl borane (TBB) dentin adhesive. Human molar teeth, extracted and stored in distilled water or 70% ethanol solution for 7 or 28 days, were treated with the resin. Spatially resolved Raman microspectroscopy was used to measure penetration. The band intensity ratio 1612 cm-1 (resin): 962 cm-1 (dentin) was used as a diagnostic. Diffusion of the resin into dentin increased with the length of storage period. The results indicate that the effects of postextraction treatments on teeth must be considered when laboratory measurements of bonding strengths are employed to predict the clinical performance of dental cements. In addition, it is demonstrated that Raman microprobe spectroscopy is a feasible analytical tool to evaluate the effects of postextraction treatments on teeth.

  12. Multi-podant diglycolamides and room temperature ionic liquid impregnated resins: An excellent combination for extraction chromatography of actinides.

    PubMed

    Gujar, R B; Ansari, S A; Verboom, W; Mohapatra, P K

    2016-05-27

    Extraction chromatography resins, prepared by impregnating two multi-podant diglycolamide ligands, viz. diglycolamide-functionalized calix[4]arene (C4DGA) and tripodal diglycolamide (T-DGA) dissolved in the room temperature ionic liquid 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide (RTIL: C4mimTf2N) on Chromosorb-W (an inert solid support), gave excellent results for the removal of trivalent actinides from acidic waste solutions. Distribution coefficient measurements on several metal ions showed selective sorption of Am(III) over hexavalent uranyl ions and other fission product elements such as strontium and cesium. The sorbed metal ions could be efficiently desorbed with a complexing solution containing guanidine carbonate and EDTA buffer. The sorption of Am(III) on both resins followed pseudo-second order rate kinetics with rate constants of 1.37×10(-6) and 6.88×10(-7)g/cpmmin for T-DGA and C4DGA resins, respectively. The metal sorption on both resins indicated the Langmuir monolayer chemisorption phenomenon with Eu(III) sorption capacities of 4.83±0.21 and 0.52±0.05mg per g of T-DGA and C4DGA resins, respectively. The results of column studies show that these resins are of interest for a possible application for the recovery of hazardous trivalent actinides from dilute aqueous solutions. PMID:27130582

  13. Curcumin and Boswellia serrata gum resin extract inhibit chikungunya and vesicular stomatitis virus infections in vitro.

    PubMed

    von Rhein, Christine; Weidner, Tatjana; Henß, Lisa; Martin, Judith; Weber, Christopher; Sliva, Katja; Schnierle, Barbara S

    2016-01-01

    Chikungunya virus (CHIKV) is a mosquito-transmitted alphavirus that causes chikungunya fever and has infected millions of people mainly in developing countries. The associated disease is characterized by rash, high fever, and severe arthritis that can persist for years. CHIKV has adapted to Aedes albopictus, which also inhabits temperate regions including Europe and the United States of America. CHIKV has recently caused large outbreaks in Latin America. No treatment or licensed CHIKV vaccine exists. Traditional medicines are known to have anti-viral effects; therefore, we examined whether curcumin or Boswellia serrata gum resin extract have antiviral activity against CHIKV. Both compounds blocked entry of CHIKV Env-pseudotyped lentiviral vectors and inhibited CHIKV infection in vitro. In addition, vesicular stomatitis virus vector particles and viral infections were also inhibited to the same extent, indicating a broad antiviral activity. Although the bioavailability of these compounds is rather poor, they might be used as a lead structure to develop more effective antiviral drugs or might be used topically to prevent CHIKV spread in the skin after mosquito bites. PMID:26611396

  14. 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)

  15. Determination of radium-228 in natural waters using extraction chromatographic resins

    SciTech Connect

    Burnett, W.C.; Cable, P.H.; Moser, R.

    1995-12-31

    We have developed a procedure for determination of {sup 228}Ra (t 1/2= 5.75 y) in natural waters using either the extraction chromatographic resins TRU-Spec{sup TM} or Ln-{center_dot}Spec{sup TM} to isolate the direct daughter, {sup 228}Ac, just before low-level counting. These separations are shown to be quantitative, simple, relatively fast, and free from most interferences. The recommended procedure effectively eliminates the need to perform the multiple precipitations and solvent extractions required by conventional techniques. The method uses a standard BaSO{sub 4} co-precipitation with {sup 133}Ba as an internal tracer to preconcentrate radium from a 1-2 L water sample. This is followed by a metathesizing process using K{sub 2}CO{sub 3} to convert the BaSO{sub 4} to the more soluble BaCO{sub 3} form. After the {sup 133}Ba yield determination, the sample (in HN0{sub 3}) is stored for {ge}30 hours to allow ingrowth of equilibrium amounts of {sup 228}Ac (t 1/2=6.14 h) from the {sup 228}Ra in the sample. This solution is then loaded onto a chromatographic column prerinsed with HN0{sub 3} followed by a rinse with sufficient HN0{sub 3} to completely flush out barium, radium, lead, and other common elements which may be contained in the sample load. Actinium is then eluted with either HCl or more concentrated HN0{sub 3} and is ready for low-level beta-particle counting after mounting by filtration or evaporation. We estimate a detection limit of {le}1.0 pCi/L in approximately 30 minutes of counting using a proportional counter with a 1.0 cpm total beta background, a {sup 133}Ba yield of 80%, and a 2-L sample volume.

  16. Separation and purification of both tea seed polysaccharide and saponin from camellia cake extract using macroporous resin.

    PubMed

    Yang, Pengjie; Zhou, Mingda; Zhou, Chengyun; Wang, Qian; Zhang, Fangfang; Chen, Jian

    2015-02-01

    A novel method to separate and purify tea seed polysaccharide and tea seed saponin from camellia cake extract by macroporous resin was developed. Among four kinds of resins (AB-8, NKA-9, XDA-6, and D4020) tested, AB-8 macroporous resin possessed optimal separating capacity for the two substances and thus was selected for the separation, in which deionized water was used to elute tea seed polysaccharide, 0.25% NaOH solution to remove the undesired pigments, and 90% ethanol to elute tea seed saponin. Further dynamic adsorption/desorption experiments on AB-8 resin-based column chromatography were conducted to obtain the optimal parameters. Under optimal dynamic adsorption and desorption conditions, 18.7 and 11.8% yield of tea seed polysaccharide and tea seed saponin were obtained with purities of 89.2 and 96.0%, respectively. The developed method provides a potential approach for the large-scale production of tea seed polysaccharide and tea seed saponin from camellia cake. PMID:25491912

  17. Impregnated resins containing di-(2-ethylhexyl) thiophosphoric acid for the extraction of palladium(II). 2: Selective palladium(II) recovery from hydrochloric acid solutions

    SciTech Connect

    Rovira, M.; Cortina, J.L.; Arnaldos, J.; Sastre, A.M.

    1999-03-01

    The extraction of Pd(II) from HCl solutions by impregnated resins containing di(2-ethylhexyl) thiophosphoric acid (DEHTPA or HL) on the Amberlite XAD2 polymeric support has been studied. Graphical and computer analysis with the program LETAGROP-DISTR demonstrated that the Pd(II) extraction can be explained by the formation of metal complexes in the resin phase having the composition PdL{sub 2}(HL){sub 2}. DEHTPA/XAD2 resins extracted Pd(II) in the presence of other metals: Pt(IV), Rh(III), Cu(II), Fe(III) as well as Zn(II). The stripping of Pd(II) loaded on the organic phase and the lifetime of the resins were also investigated.

  18. Direct measurement of elastic modulus of Nb 3Sn using extracted filaments from superconducting composite wire and resin impregnation method

    NASA Astrophysics Data System (ADS)

    Hojo, M.; Matsuoka, T.; Hashimoto, M.; Tanaka, M.; Sugano, M.; Ochiai, S.; Miyashita, K.

    2006-10-01

    Young's modulus of Nb3Sn filaments in Nb3Sn/Cu superconducting composite wire was investigated in detail. Nb3Sn filaments were first extracted from composite wire. Nitric acid and hydrofluoric acid were used to remove copper stabilizer, Nb3Sn/Nb barrier and bronze. Then, Nb3Sn filaments were impregnated with epoxy resin to form simple filament bundle composite rods. A large difference in Young's moduli of filaments and epoxy resin enhance the accuracy of the measurement of Nb3Sn filament modulus. The ratio of Nb3Sn to Nb in filaments and the number of filaments in the fiber bundle composite rods were used in the final calculation of the Young's modulus of Nb3Sn. The obtained modulus of 127 GPa was the lower bound of the already reported values.

  19. 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 interactions between the oxygen's of the ether and cations in the mobile phase. This particular resin has been shown to have an extremely high uptake affinity for Pb, a direct homolog of element 114, and is thus a good initial extractant to examine for a potential element 114 chemical system. Figure 1.1 shows the respective extractant molecules from the DGA and Pb resins. Batch uptake experiments were conducted to examine the uptake behavior of Ta on the DGA resin. Batch uptake experiments were also conducted to examine the uptake behavior of Ge on the Pb resin. Column experiments were designed based on batch uptake experiments of Ta, Am, Pa, Np, Zr, and Nb to establish a sequential extraction of Group IV/V homologs as well as Am for potential use as a Db chemical system.

  20. Solid phase extraction purification of carboxylic acid products from 96-well format solution phase synthesis with DOWEX 1x8-400 formate anion exchange resin.

    PubMed

    Bookser, B C; Zhu, S

    2001-01-01

    The anion exchange resin DOWEX 1x8-400 formate has been developed for the isolation or resin capture of carboxylic acids from solution phase reactions in a 96-well format using a batchwise solid phase extraction technique. Eleven different anion exchange resins (formate forms) were evaluated for their efficiency at scavenging aryl and aliphatic carboxylic acids from solution. The model carboxylic acids had pK(a)s ranging from 3.40 to 4.89. Exchange efficiency onto the resin was pK(a) dependent with the carboxylic acids but not with their diisopropylethylammonium salts. Exchange off of the resin also showed pK(a) dependence with the stronger acids requiring more concentrated solvent acid for exchange. DOWEX 1x8-400 formate was determined to have superior capacity and the fastest exchange rate. Solvents suitable for exchanging the acids onto the resin were CH2Cl2, methanol, and various solvent/water mixtures. Solvents suitable for exchanging the carboxylic acids off of the resin were TFA/solvent or HCO2H/solvent mixtures. The resin was found to swell best in CH2Cl2 and in polar protic solvents such as water, alcohols, and acids. Application of this technique to the crude product mixtures from an arrayed reductive amination and an arrayed Stille reaction provided product carboxylic acids in yields averaging 57% and purities averaging 89%. PMID:11300862

  1. Actinide Binding by Kläui Ligands: REDOX Speciation and Sorption on an Extraction Chromatography Resin

    SciTech Connect

    Levitskaia, Tatiana G.; Sinkov, Sergey I.; Lumetta, Gregg J.

    2008-12-01

    The sorption of Eu(III) and actinide ions in various oxidation states from nitric acid solutions by an extraction chromatography resin containing 1 wt% of the Kläui ligand Cp*Co[P(O)(OR)2]3– [Cp* = pentamethylcyclopentadienyl, R = –CH2 CH2CH3] on Amberlite® XAD-7HP was examined. At 0.3 M HNO3 and a metal-to-ligand ratio of 0.07, the relative affinity of the resin for the ions investigated followed the order: tetravalent >> hexavalent > trivalent > pentavalent; however, the relative affinity for the trivalent and hexavalent ions can be reversed, depending on the extent of ligand loading and the nitric acid concentration. The sorption of the tetravalent ions was exceptionally strong in the entire range of nitric acid concentration examined (0.2 to 8 M HNO3). Resin samples loaded with various actinide ions were examined spectrophotometrically. No Np(V) and Pu(III) species were identified on the resin; rather, reduction-oxidation (REDOX) reactions occurred during equilibration, resulting in their complete conversion to M(IV) species bound by the Kläui ligand. Similarly, the sorption behavior of Pu(VI) and Np(VI) was complicated by their reduction to M(IV) upon sorption. The observed REDOX processes were apparently driven by the extremely high affinity of the Kläui ligand for the tetravalent ions. The acid-base properties of the methyl derivative of the Kläui ligand were investigated in aqueous solution, and its pKa was found to be highly dependent upon the solution ionic strength. The binding constants of this ligand with various actinide ions measured in a mixed methanol/carbon tetrachloride solvent exhibited qualitative agreement with the sorption selectivity trends.

  2. 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, 0.37mmol g(-)(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

  3. Extraction of anthocyanins from black bean canning wastewater with macroporous resins.

    PubMed

    Wang, Xiaoxi; Hansen, Conly; Allen, Karin

    2014-02-01

    This study investigated purification of anthocyanins from black bean canning wastewater by column chromatography with 5 types of macroporous resins (Diaion Hp20, Sepabeads Sp70, Sepabeads Sp207, Sepabeads Sp700, and Sepabeads Sp710). By-product of canned black beans was partially purified by filtration, in anticipation of higher performance during column chromatography. Equilibrium adsorption isotherms were measured and analyzed using Langmuir and Freundlich isotherm models. Both Langmuir (all R² ≥ 0.98) and Freundlich (all R² ≥ 0.97) models can describe the adsorption process of anthocyanins from black bean canning wastewater using the tested resins. The adsorption and desorption behaviors of anthocyanins were studied using a dynamic method on the 5 types of resins, and Sp700 presented the highest adsorption capacity (39 ± 4 mg/g; P < 0.05) as well as desorption capacity (19 ± 2%; P < 0.05), indicating that of the resins examined, Sp700 is a better candidate for purification of anthocyanins from black bean canning wastewater. PMID:24472095

  4. A physical entrapment method for the preparation of carbon nanotube reinforced macroporous adsorption resin with enhanced selective extraction performance

    NASA Astrophysics Data System (ADS)

    Ha, Wei; Song, Xin-Yue; Chen, Juan; Shi, Yan-Ping

    2015-11-01

    In this paper, we demonstrate a novel carbon nanotube (CNT) reinforced macroporous adsorption resin (MAR) for the first time. The CNTs were dispersed in water via sonication, and then in situ physically entrapped in the pores of MAR by capillary forces and sonication. The resulting CNT reinforced MAR (CNT-MAR) was proved by transmission electron microscopy (TEM) and confocal laser scanning microscopy (CLSM), and subsequently applied to extract a mixture of 8 types, 14 natural products. For comparison, the extraction efficiency of original MAR without CNTs was also evaluated. After extraction, the supernatants were detected via high-performance liquid chromatography (HPLC). The results indicated that the introduction of carbon nanotubes (CNTs) into the pores of MAR can significantly improve the adsorptive selectivity of MAR for natural products. The original MAR without CNTs has almost the same adsorption capacity for selectively extracting 3 types of natural products (phenols, alkaloids and anthraquinones). However, the CNT-MAR only could selectively extract anthraquinones and the adsorption capacity for three anthraquinone natural products is 1.46-1.83 times higher than that of unmodified MAR. In order to achieve the highest extraction efficiency of CNT-MAR for anthraquinone natural products, the main extraction parameters such as the extraction time and the pH value were also optimized. The CNT-MAR demonstrated an excellent ability to extract anthraquinone natural products with high selectivity and adsorption capacity. Due to its low cost, easy preparation and use, and operational characteristics, it shows great potential for selective extraction of natural products.In this paper, we demonstrate a novel carbon nanotube (CNT) reinforced macroporous adsorption resin (MAR) for the first time. The CNTs were dispersed in water via sonication, and then in situ physically entrapped in the pores of MAR by capillary forces and sonication. The resulting CNT reinforced MAR (CNT-MAR) was proved by transmission electron microscopy (TEM) and confocal laser scanning microscopy (CLSM), and subsequently applied to extract a mixture of 8 types, 14 natural products. For comparison, the extraction efficiency of original MAR without CNTs was also evaluated. After extraction, the supernatants were detected via high-performance liquid chromatography (HPLC). The results indicated that the introduction of carbon nanotubes (CNTs) into the pores of MAR can significantly improve the adsorptive selectivity of MAR for natural products. The original MAR without CNTs has almost the same adsorption capacity for selectively extracting 3 types of natural products (phenols, alkaloids and anthraquinones). However, the CNT-MAR only could selectively extract anthraquinones and the adsorption capacity for three anthraquinone natural products is 1.46-1.83 times higher than that of unmodified MAR. In order to achieve the highest extraction efficiency of CNT-MAR for anthraquinone natural products, the main extraction parameters such as the extraction time and the pH value were also optimized. The CNT-MAR demonstrated an excellent ability to extract anthraquinone natural products with high selectivity and adsorption capacity. Due to its low cost, easy preparation and use, and operational characteristics, it shows great potential for selective extraction of natural products. Electronic supplementary information (ESI) available: Additional information as noted in the text. See DOI: 10.1039/c5nr05454k

  5. Use of dipicolinate-based complexes for producing ion-imprinted polystyrene resins for the extraction of yttrium-90 and heavy lanthanide cations.

    PubMed

    Chauvin, Anne-Sophie; Bünzli, Jean-Claude G; Bochud, François; Scopelliti, Rosario; Froidevaux, Pascal

    2006-09-01

    Highly selective separation of yttrium (and lanthanides) is of interest for the design of radiopharmaceuticals, and an efficient method based on the ion-imprinting concept is proposed here. The synthesis and structural, thermodynamic and photophysical characterization of complexes of trivalent yttrium and lanthanides with two new vinyl derivatives of dipicolinic acid, HL1 and L2, are described. The feasibility of using ion-imprinted resins for yttrium and lanthanide separation is demonstrated. The resins were obtained by copolymerization with styrene and divinylbenzene and subsequent acid treatment to remove the metal ion. High-resolution Eu luminescence experiments revealed that the geometry of the complexation sites is well preserved in the imprinted polymers. The ion-imprinted polymer based on HL1 proved to be particularly well adapted for yttrium extraction, having a sizeable capacity (8.9+/-0.2 mg g(-1) resin) and a fast rate of extraction (t(1/2)=1.7 min). In addition, lighter and heavier lanthanide ions are separated. Finally, the resin displays high selectivity for yttrium and lanthanide cations against alkali and alkaline earth metals. For instance, in a typical experiment, 10 mg of yttrium was extracted from 5 g of milk ash sample by 2 g of the resin. The good separation properties displayed by the resin based on HL1 open interesting perspectives for the production of highly pure (90)Y and radiolanthanides for medical applications, and for trace analysis of these radiochemicals in food and in the environment. PMID:16763951

  6. Adsorption and desorption properties of macroporous resins for anthocyanins from the calyx extract of roselle (Hibiscus sabdariffa L.).

    PubMed

    Chang, Xiu-Lian; Wang, Dong; Chen, Bi-Yun; Feng, Yong-Mei; Wen, Shao-Hong; Zhan, Peng-Yuan

    2012-03-01

    Adsorption of roselle anthocynins, a natural pigment, onto various macroporous resins was optimized to develop a simple and efficient process for industrial separation and purification of roselle anthocyanins. Nine different macroporous resins (AB-8, X-5, HPD-100, SP-207, XAD-4, LS-305A, DM-21, LS-610B, and LS-305) were evaluated for the adsorption properties of the anthocyanins extracted from the calyx extract of Hibiscus sabdariffa L. The influences of phase contact time, solution pH, initial anthocyanin concentration, and ethanol concentration with different citric acid amounts were studied by the static adsorption/desorption method. The adsorption isotherm data were fitted well to the Langmuir isotherm, and according to this model, LS-610B and LS-305 exhibited the highest monolayer sorption capacities of 31.95 and 38.16 mg/g, respectively. The kinetic data were modeled using pseudo-first-order, pseudo-second-order, and intraparticle diffusion equations. The experimental data were well described by the pseudo-second-order kinetic model. Continuous column adsorption-regeneration cycles indicated negligible capacity loss of LS-305 during operation. The overall yield of pigment product was 49.6 mg/g dried calyces. The content of roselle anthocynins in the pigment product was 4.85%. PMID:22329796

  7. Inadequacy, Impurity and Infidelity; Modifying the Modified Brendel Alpha-Cellulose Extraction Method for Resinous Woods in Stable Isotope Dendroclimatology

    NASA Astrophysics Data System (ADS)

    Brookman, T. H.; Whittaker, T. E.; King, P. L.; Horton, T. W.

    2011-12-01

    Stable isotope dendroclimatology is a burgeoning field in palaeoclimate science due to its unique potential to contribute (sub)annually resolved climate records, over millennial timescales, to the terrestrial palaeoclimate record. Until recently the time intensive methods precluded long-term climate reconstructions. Advances in continuous-flow mass spectrometry and isolation methods for α-cellulose (ideal for palaeoclimate studies as, unlike other wood components, it retains its initial isotopic composition) have made long-term, calendar dated palaeoclimate reconstructions a viable proposition. The Modified Brendel (mBrendel) α-cellulose extraction method is a fast, cost-effective way of preparing whole-wood samples for stable oxygen and carbon isotope analysis. However, resinous woods often yield incompletely processed α-cellulose using the standard mBrendel approach. As climate signals may be recorded by small (<1%) isotopic shifts it is important to investigate if incomplete processing affects the accuracy and precision of tree-ring isotopic records. In an effort to address this methodological issue, we investigated three highly resinous woods: kauri (Agathis australis), ponderosa pine (Pinus ponderosa) and huon pine (Lagarastrobus franklinii). Samples of each species were treated with 16 iterations of the mBrendel, varying reaction temperature, time and reagent volumes. Products were investigated using microscopic and bulk transmission Fourier Transform infrared spectroscopy (FITR) to reveal variations in the level of processing; poorly-digested fibres display a peak at 1520cm-1 suggesting residual lignin and a peak at ~1600cm-1 in some samples suggests retained resin. Despite the different levels of purity, replicate analyses of samples processed by high temperature digestion yielded consistent δ18O within and between experiments. All α-cellulose samples were 5-7% enriched compared to the whole-wood, suggesting that even incomplete processing at high temperature can provide acceptable δ18O analytical external precision. For kauri, short, lower temperature extractions produced α-cellulose with δ18O consistently ~1% lower than longer, higher temperature kauri experiments. These findings suggest that temperature and time are significant variables that influence the analytical precision of α-cellulose stable isotope analysis and that resinous hardwoods (e.g. kauri) may require longer and/or hotter digestions than softwoods. The effects of mBrendel variants on the carbon isotope ratio precision of α-cellulose extracts will also be presented. Our findings indicate that the standard mBrendel α-cellulose extraction method may not fully remove lignins and resins depending on the type of wood being analysed. Residual impurities can decrease analytical precision and accuracy. Fortunately, FTIR analysis prior to isotopic analysis is a relatively fast and cost effective way to determine α-cellulose extract purity, ultimately improving the data quality, accuracy and utility of tree-ring based stable isotopic climate records.

  8. Ethanolic extract of Commiphora mukul gum resin attenuates streptozotocin-induced alterations in carbohydrate and lipid metabolism in rats

    PubMed Central

    Ramesh, B.; Karuna, R.; Sreenivasa Reddy, S.; Sudhakara, G.; Saralakumari, D.

    2013-01-01

    The purpose of this study was to investigate the effects of Commiphora mukul gum resin ethanolic extract (CMEEt) administration against altered activities of key enzymes of carbohydrate metabolism, lipid metabolism and changes in glycogen content (liver and muscle) and lipids (liver and heart) in streptozotocin (STZ) induced insulin deficient diabetic Wistar albino rats. Diabetes was induced by intraperitoneal injection of STZ (55 mg/kg body wt) to male Wistar rats. The animals were divided into four groups: Control (C), control-treated (C+CM), diabetic (D) and diabetic-treated group (D+CM). Diabetic-treated and control-treated rats were treated with C. mukul gum resin ethanolic extract (CMEEt) in 2 ml distilled water, orally (200 mg/kg body weight/day for 60 days). At the end of the experimental period, biochemical parameters related to carbohydrate and lipid metabolism were assayed. The significant enhancement in tissue lipids (heart and liver) total cholesterol, triglycerides, phospholipids and free fatty acids of diabetic rats were nearer to normalized in diabetic treated rats (D+CM). Alterations in the activities of enzymes of glucose metabolism (hexokinase, phosphofructokinase, pyruvate kinase, and glucose-6-phosphatase, fructose-1,6-bisphosphatase and glucose-6-phosphate dehydrogenase) and lipid metabolism (fatty acid synthase, malic enzyme and lipoprotein lipase) as observed in diabetic (D) rats were prevented with CMEEt administration. In conclusion, our findings indicate improvement of glucose and lipid metabolisms in STZ induced diabetic rats by treatment with Commiphora mukul and suggest that the plant can be used as an adjuvant for the prevention and/or management of insulin deficiency and disorder related to it. PMID:27004047

  9. Method for recovering and using lignin in adhesive resins by extracting demethylated lignin

    DOEpatents

    Schroeder, Herbert A.

    1991-01-01

    Lignin, or a lignin derived material, which has been significantly demethylated (e.g., the demethylated lignin found in the raffinate produced as a by-product of dimethyl sulfide production which can be carried out using the spent liquor from wood pulping operations) can be isolated by a process wherein an organic solvent is added to a lignin-containing aqueous solution. The organic solvent is typically a polar, and at least a partially water-immiscible substance such as, for example, ethyl acetate. The resulting lignin-containing aqueous solution/organic solvent mixture is acidified to produce a water layer which is discarded and an organic solvent layer which contains the demethylated lignin. Upon its recovery, the demethylated lignin is dissolved in an alkaline solution to which an aldehyde source is added to produce a resol-type resin. The aldehyde source may be formaldehyde in solution, paraformaldehyde, hexamethylenetetramine, or other aldehydes including acetaldehyde, furfural, and their derivatives.

  10. Resistant behavior of a novel silica-based octyl(phenyl)- N, N-diisobutyl carbamoylmethylphoshine oxide neutral extraction resin against nitric acid, temperature and γ-radiation

    NASA Astrophysics Data System (ADS)

    Zhang, Anyun; Wei, Yuezhou; Kumagai, Mikio; Koma, Yoshikazu; Koyama, Tomozo

    2005-03-01

    The resistant behavior of a novel silica-based octyl(phenyl)- N, N-diisobutylcarbamoyl-methylphoshine oxide (CMPO) extraction resin (CMPO/SiO 2-P) against HNO 3, temperature and γ-radiation had been investigated. The adsorption properties of the treated CMPO/SiO 2-P resin were evaluated by a 3 M HNO 3 solution containing 0.01 M Nd(III). It was found that 3 M or 0.01 M HNO 3 concentration did not decrease the stability of CMPO/SiO 2-P at 25°C. The HNO 3 concentration effect on the leakage of CMPO/SiO 2-P resin at 80°C was obviously higher than that of at 25°C. The adsorbed amount of Nd(III) onto the treated CMPO/SiO 2-P resin was determined in the range of 0.1769-0.1839 mmol/g, which basically approached to 0.1875 mmol/g, the adsorbed quantity of fresh CMPO/SiO 2-P resin for Nd(III). The contents of P and C leaked from CMPO/SiO 2-P resin obviously increased with an increase in the radiation dose ( ID) from 1.0 to 4.1 MGy in terms of the linear equations: [P]=110.05 ID+21.92 and [C]=7683.8 ID-919.8. The adsorbed amount of Nd(III) onto the radiated CMPO/SiO 2-P resin quickly decreased from 0.1499 to 0.0900 mmol/g according to the equation QNd(III)=-0.0222 ID+0.1778, showing a large quantity of CMPO leaked from CMPO/SiO 2-P resin.

  11. Phosphonic acid based exchange resins

    DOEpatents

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

    1995-09-12

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

  12. Phosphonic acid based exchange resins

    DOEpatents

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

    1995-01-01

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

  13. Separation of cyclotron-produced 44Sc from a natural calcium target using a dipentyl pentylphosphonate functionalized extraction resin

    PubMed Central

    Valdovinos, H.F.; Hernandez, R.; Barnhart, T.E.; Graves, S.; Cai, W.; Nickles, R.J.

    2014-01-01

    Significant interest in 44Sc as a radioactive synthon to label small molecules for positron emission tomography (PET) imaging has been recently observed. Despite the efforts of several research groups, the ideal 44Sc production and separation method remains elusive. Herein, we propose a novel separation method to obtain 44Sc from the proton irradiation of calcium targets based on extraction chromatography, which promises to greatly simplify current production methodologies. Using the commercially available Uranium and Tetravalent Actinides (UTEVA) extraction resin we were able to rapidly (< 20 min) recover > 80% of the activity generated at end of bombardment (EoB) in small ~1 M HCl fractions (400 μL). The chemical purity of the 44Sc eluates was evaluated through chelation with DOTA and DTPA, and by trace metal analysis using microwave induced plasma atomic emission spectrometry. The distribution coefficients (Kd) of Sc(III) and Ca(II) in UTEVA were determined in HCl medium in a range of concentrations from zero to 12.1 M The 44Sc obtained with our method proved to be suitable for the direct labeling of small biomolecules for PET imaging, with excellent specific activities and radiochemical purity. PMID:25464172

  14. Separation of cyclotron-produced (44)Sc from a natural calcium target using a dipentyl pentylphosphonate functionalized extraction resin.

    PubMed

    Valdovinos, H F; Hernandez, R; Barnhart, T E; Graves, S; Cai, W; Nickles, R J

    2014-10-01

    Significant interest in (44)Sc as a radioactive synthon to label small molecules for positron emission tomography (PET) imaging has been recently observed. Despite the efforts of several research groups, the ideal (44)Sc production and separation method remains elusive. Herein, we propose a novel separation method to obtain (44)Sc from the proton irradiation of calcium targets based on extraction chromatography, which promises to greatly simplify current production methodologies. Using the commercially available Uranium and Tetravalent Actinides (UTEVA) extraction resin we were able to rapidly (<20min) recover >80% of the activity generated at end of bombardment (EoB) in small ~1M HCl fractions (400μL). The chemical purity of the (44)Sc eluates was evaluated through chelation with DOTA and DTPA, and by trace metal analysis using microwave induced plasma atomic emission spectrometry. The distribution coefficients (Kd) of Sc(III) and Ca(II) in UTEVA were determined in HCl medium in a range of concentrations from zero to 12.1M. The (44)Sc obtained with our method proved to be suitable for the direct labeling of small biomolecules for PET imaging, with excellent specific activities and radiochemical purity. PMID:25464172

  15. Tunable aqueous polymer-phase impregnated resins-technology-a novel approach to aqueous two-phase extraction.

    PubMed

    van Winssen, F A; Merz, J; Schembecker, G

    2014-02-14

    Aqueous Two-Phase Extraction (ATPE) represents a promising unit operation for downstream processing of biotechnological products. The technique provides several advantages such as a biocompatible environment for the extraction of sensitive and biologically active compounds. However, the tendency of some aqueous two-phase systems to form intensive and stable emulsions can lead to long phase separation times causing an increased footprint for the required mixer-settler devices or the need for additional equipment such as centrifuges. In this work, a novel approach to improve ATPE for downstream processing applications called 'Tunable Aqueous Polymer-Phase Impregnated Resins' (TAPPIR(®))-Technology is presented. The technology is based on the immobilization of one aqueous phase inside the pores of a solid support. The second aqueous phase forms the bulk liquid around the impregnated solids. Due to the immobilization of one phase, phase emulsification and phase separation of ATPE are realized in a single step. In this study, a biodegradable and sustainable aqueous two-phase system consisting of aqueous polyethylene glycol/sodiumcitrate solutions was chosen. The impregnation of different macroporous glass and ceramic solids was investigated and could be proven to be stable. Additionally, the separation of the dye Patent blue V was successfully performed with the TAPPIR(®)-Technology. Thus, the "proof of principle" of this technology is presented. PMID:24462465

  16. Mechanistic Study of Silver Nanoparticle's Synthesis by Dragon's Blood Resin Ethanol Extract and Antiradiation Activity.

    PubMed

    Hasan, Murtaza; Iqbal, Javed; Awan, Umer; Saeed, Yasmeen; Ranran, Yuan; Liang, Yanli; Dai, Rongji; Deng, Yulin

    2015-02-01

    Biological synthesis of nanoparticles is best way to avoid exposure of hazardous materials as compared to chemical manufacturing process which is a severe threat not only to biodiversity but also to environment. In present study, we reported a novel method of finding antiradiation compounds by bioreducing mechanism of silver nanoparticles formation using 50% ethanol extract of Dragons blood, a famous Chinese herbal plant. Color change during silver nanoparticles synthesis was observed and it was confirmed by ultra violet (UV) visible spectroscopy at wave length at 430 nm after 30 min of reaction at 60 °C. Well dispersed round shaped silver nanoparticles with approximate size (4 nm to 50 nm) were measured by TEM and particle size analyser. Capping of biomolecules on Ag nanoparticles was characterized by FTIR spectra. HPLC analysis was carried out to find active compounds in the extract. Furthermore, antiradiation activity of this extract was tested by MTT assay in vitro after incubating the SH-SY5Y cells for 24 h at 37 °C. The results indicate that presence of active compounds in plant extract not only involves in bioreduction process but also shows response against radiation. The dual role of plant extract as green synthesis of nanoparticles and exhibit activity against radiation which gives a new way of fishing out active compounds from complex herbal plants. PMID:26353649

  17. Inhibition of leukotriene B4 formation in rat peritoneal neutrophils by an ethanolic extract of the gum resin exudate of Boswellia serrata.

    PubMed

    Ammon, H P; Mack, T; Singh, G B; Safayhi, H

    1991-06-01

    Suspensions of rat peritoneal polymorphonuclear leukocytes (PMNL) elicited with glycogen were stimulated by calcium and ionophore to produce leukotrienes and 5-HETE from endogenous arachidonic acid (AA). We investigated the effect of ethanolic extracts of the gum resin exudate of Boswellia serrata. A concentration-dependent inhibition of LTB4 and 5-HETE production by different charges of exudate extracts were found. All products of the 5-lipoxygenase (5-LOx) from endogenous arachidonic acid (AA) in PMNL were reduced to the same extent by the extracts tested. The ethanolic extract of the gum resin also decreased 5-LOx mediated metabolisation of exogenously added AA to LTB4 and 5-HETE. Since steroidal-type anti-inflammatory drugs do not exert an immediate effect in the test system used, we conclude that the activity of the 5-LOx itself represents the side of inhibition by the gum resin extract. Therefore, an inhibition of 5-LOx catalysed mediator synthesis might be involved in the previously reported anti-inflammatory activity in vivo. PMID:1654575

  18. Comparison of Apical Microleakage of Dual-Curing Resin Cements with Fluid-Filtration and Dye Extraction Techniques

    PubMed Central

    Kaya, Sadullah; Özer, Senem Yiğit; Adigüzel, Özkan; Oruçoğlu, Hasan; Değer, Yalçın; Tümen, Emin Caner; Uysal, İbrahim

    2015-01-01

    Background Endodontically treated teeth with excessive loss of tooth structure are frequently restored using fiber posts. In this in vitro study, the apical leakage of self- and dual-activated curing modes for dual-curing resins cementing a translucent fiber post was evaluated using computerized fluid filtration meter and dye extraction method. Material/Methods One hundred and four extracted human maxillary incisors with single root and canal were used. Experimental samples embedded in a closed system were divided into 4 groups (n=20) according to 2 dual-curing luting systems, with 2 different curing modes (either with self- or light-activation): (1) Panavia F 2.0 with self-cure, (2) Panavia F 2.0 with light-activation, (3) Clearfill SA with self-cure, and (4) Clearfill SA with light activation. Twenty-four teeth served as negative and positive controls. Translucent fiber posts were luted in the roots except in the control groups. Results Statistical analysis indicated no significant difference in leakage among groups (p>0.05) with 4.12×10−4 (Panavia self-cure), 4.55×10−4 (Clearfill SA self-cure), 5.17×10−4 (Panavia dual-cure), and 5.59×10−4 (Clearfill SA dual-cure) in fluid-filtration method. Absorbance values for dye-extraction method were 266 nanometer (nm) (Panavia self-cure), 268 nm (Clearfill SA self-cure), 270 nm (Panavia dual-cure), and 271 nm (Clearfill SA dual-cure), in which difference among the groups were not statistically significant (p>0.05). When comparing the leakage, assessment methods results showed no statistically significant difference between the tested evaluation techniques (p>0.05). Conclusions Light- and self-activation curing modes of Panavia F 2.0 and Clearfill SA perform similar to each other in a closed system. PMID:25824712

  19. Optimizing light collection from extractive scintillating resin in flow-cell detectors

    NASA Astrophysics Data System (ADS)

    Meldrum, Amy Catherine

    The objectives of this study were to investigate the changes in light collection efficiency for flow cell detector as various parameters are altered to find the optimum flow cell configuration. Columns with inner diameters of 0.16 cm, 0.48 cm, 0.79 cm, and 1.11 cm were packed with synthesized nonporous, un-functionalized beads to measure their detection efficiencies for solutions containing 210Po, 14C, or 90Sr/ 90Y. The average diameter of the beads used in the experiments was 147 microm +/- 33 microm. The highest detection efficiency for 210Po was 15.3 +/- 3.9% with the 1.11 cm diameter column. The 1.11 cm diameter column also yielded the highest detection efficiency of 29.6 +/- 0.8% for 14C. When filled with a 90Sr/ 90Y solution, the 0.79 cm diameter column had the highest detection efficiency of 100 +/- 7.0%. However, for both 14C and 90Sr/90Y, the 0.48 cm, 0.79 cm, and 1.11 cm diameter columns had detection efficiencies within 1-sigma of each other. To investigate the effects of various parameters on the light collection efficiency and detection efficiency, models were built using GATE (GEANT4 Application for Tomographic Emissions) to simulate the columns. Bead diameter, column inner diameter, and source location were varied within the simulations, for beads that were arranged in a body-centered-cubic (BCC) configuration. The highest detection efficiency for 210Po was a point source located within each bead approximately 100 +/- 1.3 %, regardless of column inner diameter or bead diameter. The same was found to be true for both 14C and 90Sr/90Y, wherein the point source configuration yielded the highest detection efficiencies of 93.1 +/- 0.3% and 98.9 +/- 0.2%, respectively, which were approximately equal regardless of bead or column size. These results suggest that if a porous resin were to be synthesized such that the radionuclide of interest could be trapped within a bead, high detection efficiencies could be achieved even with a column with a small inner diameter.

  20. Characterization and Application of Superlig 620 Solid Phase Extraction Resin for Automated Process Monitoring of 90Sr

    SciTech Connect

    Devol, Timothy A.; Clements, John P.; Farawila, Anne F.; O'Hara, Matthew J.; Egorov, Oleg; Grate, Jay W.

    2009-11-30

    Characterization of SuperLig® 620 solid phase extraction resin was performed in order to develop an automated on-line process monitor for 90Sr. The main focus was on strontium separation from barium, with the goal of developing an automated separation process for 90Sr in high-level wastes. High-level waste contains significant 137Cs activity, of which 137mBa is of great concern as an interference to the quantification of strontium. In addition barium, yttrium and plutonium were studied as potential interferences to strontium uptake and detection. A number of complexants were studied in a series of batch Kd experiments, as SuperLig® 620 was not previously known to elute strontium in typical mineral acids. The optimal separation was found using a 2M nitric acid load solution with a strontium elution step of ~0.49M ammonium citrate and a barium elution step of ~1.8M ammonium citrate. 90Sr quantification of Hanford high-level tank waste was performed on a sequential injection analysis microfluidics system coupled to a flow-cell detector. The results of the on-line procedure are compared to standard radiochemical techniques in this paper.

  1. Enhancement of 6-pentyl-α-pyrone fermentation activity in an extractive liquid-surface immobilization (Ext-LSI) system by mixing anion-exchange resin microparticles.

    PubMed

    Oda, Shinobu; Michihata, Sayumi; Sakamoto, Naoki; Horibe, Hideo; Kono, Akihiko; Ohashi, Shinichi

    2012-12-01

    The addition of anion-exchange resin microparticles into a polyacrylonitrile (PAN) ballooned microsphere layer drastically enhanced the fermentative activity of Trichoderma atroviride AG2755-5NM398 in an extractive liquid-surface immobilization (Ext-LSI) system. The production of 6-pentyl-α-pyrone (6PP), a fungicidal secondary metabolite, was 1.92-fold higher than the control (PAN alone). PMID:22871800

  2. 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.

  3. Application of ionic liquids in vacuum microwave-assisted extraction followed by macroporous resin isolation of three flavonoids rutin, hyperoside and hesperidin from Sorbus tianschanica leaves.

    PubMed

    Gu, Huiyan; Chen, Fengli; Zhang, Qiang; Zang, Jing

    2016-03-01

    Rutin, hyperoside and hesperidin were effectively extracted from Sorbus tianschanica leaves by an ionic liquid vacuum microwave-assisted method. A series of ionic liquids with various anions and alkyl chain length of the cations were studied and the extraction was performed in [C6mim][BF4] aqueous solution. After optimization by a factorial design and response surface methodology, total extraction yield of 2.37mg/g with an error of 0.12mg/g (0.71±0.04mg/g, 1.18±0.06mg/g and 0.48±0.02 for rutin, hyperoside and hesperidin, respectively) was achieved under -0.08MPa for vacuum, 19min and 420W for microwave irradiation time and power, and 15mL/g for liquid-solid ratio. The proposed method here is more efficient and needs a shorter extraction time for rutin, hyperoside and hesperidin from S. tianschanica leaves than reference extraction techniques. In stability studies performed with standard rutin, hyperoside and hesperidin, the target analytes were stable under the optimum conditions. The proposed method had a high reproducibility and precision. In addition, separation of rutin, hyperoside and hesperidin from [C6mim][BF4] extraction solution was completed effectively by AB-8 macroporous resin adsorption and desorption process. Ionic liquid vacuum microwave-assisted extraction is a simple, rapid and efficient sample extraction technique. PMID:26874229

  4. Speciation of Cr(III) and Cr(VI) in environmental samples by solid phase extraction on Ambersorb 563 resin.

    PubMed

    Narin, Ibrahim; Surme, Yavuz; Soylak, Mustafa; Dogan, Mehmet

    2006-08-25

    A simple and sensitive method for the speciation, separation and preconcentration of Cr(VI) and Cr(III) in natural water, soil and sediment samples was developed. Cr(VI) has been separated from Cr(III) and preconcentrated as Cr(III)-diphenylcarbazone complex by using Ambersorb 563 resin and determined by spectrophotometric method at 540 nm. Effect of analytical parameters such as sulfuric acid concentration, ligand volume, type of elution solution, sample volume, amount of resin and foreign ions were investigated. The presented procedure was successfully applied for the chromium speciation in various environmental samples with successfully results. PMID:16442725

  5. Final report on the safety assessment of capsicum annuum extract, capsicum annuum fruit extract, capsicum annuum resin, capsicum annuum fruit powder, capsicum frutescens fruit, capsicum frutescens fruit extract, capsicum frutescens resin, and capsaicin.

    PubMed

    2007-01-01

    Capsicum-derived ingredients function as skin-conditioning agents--miscellaneous, external analgesics, flavoring agents, or fragrance components in cosmetics. These ingredients are used in 19 cosmetic products at concentrations as high as 5%. Cosmetic-grade material may be extracted using hexane, ethanol, or vegetable oil and contain the full range of phytocompounds that are found in the Capsicum annuum or Capsicum frutescens plant (aka red chiles), including Capsaicin. Aflatoxin and N-nitroso compounds (N-nitrosodimethylamine and N-nitrosopyrrolidine) have been detected as contaminants. The ultraviolet (UV) absorption spectrum for Capsicum Annuum Fruit Extract indicates a small peak at approximately 275 nm, and a gradual increase in absorbance, beginning at approximately 400 nm. Capsicum and paprika are generally recognized as safe by the U.S. Food and Drug Administration for use in food. Hexane, chloroform, and ethyl acetate extracts of Capsicum Frutescens Fruit at 200 mg/kg resulted in death of all mice. In a short-term inhalation toxicity study using rats, no difference was found between vehicle control and a 7% Capsicum Oleoresin solution. In a 4-week feeding study, red chilli (Capsicum annuum) in the diet at concentrations up to 10% was relatively nontoxic in groups of male mice. In an 8-week feeding study using rats, intestinal exfoliation, cytoplasmic fatty vacuolation and centrilobular necrosis of hepatocytes, and aggregation of lymphocytes in the portal areas were seen at 10% Capsicum Frutescens Fruit, but not 2%. Rats fed 0.5 g/kg day-1 crude Capsicum Fruit Extract for 60 days exhibited no significant gross pathology at necropsy, but slight hyperemia of the liver and reddening of the gastric mucosa were observed. Weanling rats fed basal diets supplemented with whole red pepper at concentrations up to 5.0% for up to 8 weeks had no pathology of the large intestines, livers, and kidneys, but destruction of the taste buds and keratinization and erosion of the gastrointestinal (GI) tract were noted in groups fed 0.5% to 5.0% red pepper. The results of 9-and 12-month extension of this study showed normal large intestines and kidneys. In rabbits fed Capsicum Annuum Powder at 5 mg/kg day-1 in the diet daily for 12 months damage to the liver and spleen was noted. A rabbit skin irritation test of Capsicum Annuum Fruit Extract at concentrations ranging from 0.1% to 1.0% produced no irritation, but Capsicum Frutescens Fruit Extract induced concentration-dependent (at 25 to 500 microg/ml) cytotoxicity in a human buccal mucosa fibroblast cell line. An ethanol extract of red chili was mutagenic in Salmonella typhimurium TA98, but not in TA100, or in Escherichia coli. Other genotoxicity assays gave a similar pattern of mixed results. Adenocarcinoma of the abdomen was observed in 7/20 mice fed 100 mg red chilies per day for 12 months; no tumors were seen in control animals. Neoplastic changes in the liver and intestinal tumors were observed in rats fed red chili powder at 80 mg/kg day-1 for 30 days, intestinal and colon tumors were seen in rats fed red chili powder and 1,2-dimethyl hydrazine, but no tumors were observed in controls. In another study in rats, however, red chile pepper in the diet at the same dose decreased the number of tumors seen with 1,2-dimethylhydrazine. Other feeding studies evaluated the effect of red chili peppers on the incidence of stomach tumors produced by N-methyl-N'-nitro-N-nitrosoguanidine, finding that red pepper had a promoting effect. Capsicum Frutescens Fruit Extract promoted the carcinogenic effect of methyl(acetoxymethyl)nitrosamine (carcinogen) or benzene hexachloride (hepatocarcinogen) in inbred male and female Balb/c mice dosed orally (tongue application). Clinical findings include symptoms of cough, sneezing, and runny nose in chili factory workers. Human respiratory responses to Capsicum Oleoresin spray include burning of the throat, wheezing, dry cough, shortness of breath, gagging, gasping, inability to breathe or speak, and, rarely, cyanosis, apnea, and respiratory arrest. A trade name mixture containing 1% to 5% Capsicum Frutescens Fruit Extract induced very slight erythema in 1 of 10 volunteers patch tested for 48 h. Capsicum Frutescens Fruit Extract at 0.025% in a repeated-insult patch test using 103 subjects resulted in no clinically meaningful irritation or allergic contact dermatitis. One epidemiological study indicated that chili pepper consumption may be a strong risk factor for gastric cancer in populations with high intakes of chili pepper; however, other studies did not find this association. Capsaicin functions as an external analgesic, a fragrance ingredient, and as a skin-conditioning agent--miscellaneous in cosmetic products, but is not in current use. Capsaicin is not generally recognized as safe and effective by the U.S. Food and Drug Administration for fever blister and cold sore treatment, but is considered to be safe and effective as an external analgesic counterirritant. Ingested Capsaicin is rapidly absorbed from the stomach and small intestine in animal studies. Subcutaneous injection of Capsaicin in rats resulted in a rise in the blood concentration, reaching a maximum at 5 h; the highest tissue concentrations were in the kidney and lowest in the liver. In vitro percutaneous absorption of Capsaicin has been demonstrated in human, rat, mouse, rabbit, and pig skin. Enhancement of the skin permeation of naproxen (nonsteroidal anti-inflammatory agent) in the presence of Capsaicin has also been demonstrated. Pharmacological and physiological studies demonstrated that Capsaicin, which contains a vanillyl moiety, produces its sensory effects by activating a Ca2 +-permeable ion channel on sensory neurons. Capsaicin is a known activator of vanilloid receptor 1. Capsaicin-induced stimulation of prostaglandin biosynthesis has been shown using bull seminal vesicles and rheumatoid arthritis synoviocytes. Capsaicin inhibits protein synthesis in Vero kidney cells and human neuroblastoma SHSY-5Y cells in vitro, and inhibits growth of E. coli, Pseudomonas solanacearum, and Bacillus subtilis bacterial cultures, but not Saccharomyces cerevisiae. Oral LD50 values as low as 161.2 mg/kg (rats) and 118.8 mg/kg (mice) have been reported for Capsaicin in acute oral toxicity studies, with hemorrhage of the gastric fundus observed in some of the animals that died. Intravenous, intraperitoneal, and subcutaneous LD50 values were lower. In subchronic oral toxicity studies using mice, Capsaicin produced statistically significant differences in the growth rate and liver/body weight increases. Capsaicin is an ocular irritant in mice, rats, and rabbits. Dose-related edema was observed in animals receiving Capsaicin injections into the hindpaw (rats) or application to the ear (mice). In guinea pigs, dinitrochlorobenzene contact dermatitis was enhanced in the presence of Capsaicin, injected subcutaneously, whereas dermal application inhibited sensitization in mice. Immune system effects have been observed in neonatal rats injected subcutaneously with Capsaicin. Capsaicin produced mixed results in S. typhimurium micronucleus and sister-chromatid exchange genotoxicity assays. Positive results for Capsaicin were reported in DNA damage assays. Carcinogenic, cocarcinogenic, anticarcinogenic, antitumorigenic, tumor promotion, and anti-tumor promotion effects of Capsaicin have been reported in animal studies. Except for a significant reduction in crown-rump length in day 18 rats injected subcutaneously with Capsaicin (50 mg/kg) on gestation days 14, 16, 18, or 20, no reproductive or developmental toxicity was noted. In pregnant mice dosed subcutaneously with Capsaicin, depletion of substance P in the spinal cord and peripheral nerves of pregnant females and fetuses was noted. In clinical tests, nerve degeneration of intracutaneous nerve fibers and a decrease in pain sensation induced by heat and mechanical stimuli were evident in subjects injected intradermally with Capsaicin. An increase in mean inspiratory flow was reported for eight normal subjects who inhaled nebulized 10(-7) M Capsaicin. The results of provocative and predictive tests involving human subjects indicated that Capsaicin is a skin irritant. Overall, studies suggested that these ingredients can be irritating at low concentrations. Although the genotoxicity, carcinogenicity, and tumor promotion potential of Capsaicin have been demonstrated, so have opposite effects. Skin irritation and other tumor-promoting effects of Capsaicin appear to be mediated through interaction with the same vanilloid receptor. Given this mechanism of action and the observation that many tumor promoters are irritating to the skin, the Panel considered it likely that a potent tumor promoter may also be a moderate to severe skin irritant. Thus, a limitation on Capsaicin content that would significantly reduce its skin irritation potential is expected to, in effect, lessen any concerns relating to tumor promotion potential. Because Capsaicin enhanced the penetration of an anti-inflammatory agent through human skin, the Panel recommends that care should be exercised in using ingredients that contain Capsaicin in cosmetic products. The Panel advised industry that the total polychlorinated biphenyl (PCB)/pesticide contamination should be limited to not more than 40 ppm, with not more than 10 ppm for any specific residue, and agreed on the following limitations for other impurities: arsenic (3 mg/kg max), heavy metals (0.002% max), and lead (5 mg/kg max). Industry was also advised that aflatoxin should not be present in these ingredients (the Panel adopted < or =15 ppb as corresponding to "negative" aflatoxin content), and that ingredients derived from Capsicum annuum and Capsicum Frutescens Plant species should not be used in products where N-nitroso compounds may be formed. (ABSTRACT TRUNCATED) PMID:17365137

  6. 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.

  7. Phosphonic acid based ion exchange resins

    DOEpatents

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

    1996-07-23

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

  8. Phosphonic acid based ion exchange resins

    DOEpatents

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

    1994-01-01

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

  9. Phosphonic acid based ion exchange resins

    DOEpatents

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

    1996-01-01

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

  10. Single vial sample preparation of markers of nerve agents by dispersive solid-phase extraction using magnetic strong anion exchange resins.

    PubMed

    Singh, Varoon; Chinthakindi, Sridhar; Purohit, Ajay Kumar; Pardasani, Deepak; Tak, Vijay; Dubey, Devendra Kumar

    2015-05-22

    A sample preparation method involving extraction, enrichment and derivatization of acidic degradation products of nerve agents was developed using magnetic strong anion exchange resins (MSAX). The method was performed in a single vial involving magnetic dispersive solid phase extraction (MDSPE). Analytes were derivatized with N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA) in the presence of resins. MSAX were custom synthesized using Fe3O4 nanoparticles as core, 4-vinylpyridine-co-divinylbenzene as polymer shell and quaternary pyridinium function as anion-exchanger. Hydroxide ions were the counter-anions of MSAX to effectively capture the acidic alkyl alkylphosphonic acids (AAPAs) and alkylphosphonic acids (APAs). Quantitative measurements of analytes were performed in the selected ion monitoring mode of GC-MS. Full scan mode of analysis was followed for identifications. Under the optimized conditions analytes were recovered in the range of 39.7-98.8% (n=3, relative standard deviations (RSD) from 0.3 to 6.5%). Limits of detection (LODs) were in the range of 0.1-1.1ngmL(-1); and the linear dynamic range was 5-1000ngmL(-1) with r(2) of 0.9977-0.9769. Applicability of the method was tested with rain-, tap-, muddy-water and Organization for Prohibition of Chemical Weapons (OPCW) Proficiency Test samples. PMID:25863924

  11. Chelating resin-based extraction of DNA from dental pulp and sex determination from incinerated teeth with Y-chromosomal alphoid repeat and short tandem repeats.

    PubMed

    Tsuchimochi, Tsukasa; Iwasa, Mineo; Maeno, Yoshitaka; Koyama, Hiroyoshi; Inoue, Hiroyuki; Isobe, Ichiro; Matoba, Ryoji; Yokoi, Motoo; Nagao, Masataka

    2002-09-01

    A procedure utilizing Chelex 100, chelating resin, was adapted to extract DNA from dental pulp. The procedure was simple and rapid, involved no organic solvents, and did not require multiple tube transfers. The extraction of DNA from dental pulp using this method was as efficient, or more so, than using proteinase K and phenol-chloroform extraction. In this study, the Chelex method was used with amplification and typing at Y-chromosomal loci to determine the effects of temperature on the sex determination of the teeth. The extracted teeth were incinerated in a dental furnace for 2 minutes at 100 degrees C, 200 degrees C, 300 degrees C, 400 degrees C, and 500 degrees C. After the isolation of DNA from the dental pulp by the Chelex method, alphoid repeats, and short tandem repeats, the human Y chromosome (DYZ3), DYS19, SYS389, DYS390, and DYS393 could be amplified and typed in all samples incinerated at up to 300 degrees C for 2 minutes. The DYS389 locus in some samples could not be amplified at 300 degrees C for 2 minutes. An autopsy case is described in which genotypings of DYS19, DYS390, and DYS393 from dental pulp obtained from a burned body were needed. The data presented in this report suggest that Chelex 100-based DNA extraction, amplification, and typing are possible in burned teeth in forensic autopsy cases. PMID:12198355

  12. Ionic liquid-based vacuum microwave-assisted extraction followed by macroporous resin enrichment for the separation of the three glycosides salicin, hyperin and rutin from Populus bark.

    PubMed

    Chen, Fengli; Mo, Kailin; Liu, Zhaizhi; Yang, Fengjian; Hou, Kexin; Li, Shuangyang; Zu, Yuangang; Yang, Lei

    2014-01-01

    An effective ionic liquid vacuum microwave-assisted method was developed for extraction of the thermo- and oxygen-sensitive glycosides salicin, hyperin and rutin from Populus bark due to the strong solvating effects of ionic liquids on plant cell walls. In this study, [C4mim]BF4 solution was selected as the extracting solution for extraction of the target analytes. After optimization by single factor experiments and response surface methodology, the optimum condition parameters were achieved, which included 1.0 M [C4mim]BF4, 2 h soaking time, -0.08 MPa vacuum, 20 min microwave irradiation time, 400 W microwave irradiation power and 25 mL/g liquid/solid ratio. Under the optimum conditions, higher extraction yields of salicin (35.53 mg/g), hyperin (1.32 mg/g) and rutin (2.40 mg/g) were obtained. Compared with other extraction methods, the developed method provided higher yields of the three target components after a relatively shorter extraction time (20 min). No obvious degradation of the target analytes was observed under the optimum conditions in performed stability studies and the proposed method had a high reproducibility. Meanwhile, after adsorption and desorption on macroporous D101 resin, the target analytes can be effectively separated from the [C4mim]BF4 ionic liquid extraction solution and the yields of salicin, hyperin and rutin were 89%, 82% and 84%, respectively. The recovered [C4mim]BF4 ionic liquid presented a good extraction effect on the three analytes after recycling five times. PMID:25004075

  13. Application of alkyl polyglycoside surfactant in ultrasonic-assisted extraction followed by macroporous resin enrichment for the separation of vitexin-2″-O-rhamnoside and vitexin from Crataegus pinnatifida leaves.

    PubMed

    Han, Feng; Guo, Yupin; Gu, Huiyan; Li, Fenglan; Hu, Baozhong; Yang, Lei

    2016-02-15

    An alkyl polyglycoside (APG) surfactant was used in ultrasonic-assisted extraction to effectively extract vitexin-2″-O-rhamnoside (VOR) and vitexin (VIT) from Crataegus pinnatifida leaves. APG0810 was selected as the surfactant. The extraction process was optimized for ultrasonic power, the APG concentration, ultrasonic time, soaking time, and liquid-solid ratio. The proposed approach showed good recovery (99.80-102.50% for VOR and 98.83-103.19% for VIT) and reproducibility (relative standard deviation, n=5; 3.7% for VOR and 4.2% for VIT) for both components. The proposed sample preparation method is both simple and effective. The use of APG for extraction of key herbal ingredients shows great potential. Ten widely used commercial macroporous resins were evaluated in a screening study to identify a suitable resin for the separation and purification of VOR and VIT. After comparing static and dynamic adsorption and desorption processes, HPD100B was selected as the most suitable resin. After column adsorption and desorption on this resin, the target compounds VOR and VIT can be effectively separated from the APG0810 extraction solution. Recoveries of VOR and VIT were 89.27%±0.42% and 85.29%±0.36%, respectively. The purity of VOR increased from 35.0% to 58.3% and the purity of VIT increased from 12.5% to 19.9%. PMID:26807707

  14. Determination of trace concentrations of actinides in the NIST bone ash standard reference material using TRU-Spec{trademark} extraction resin

    SciTech Connect

    Lin, Z.; Inn, K.G.W.; Hernandez, C.E.C.

    1995-12-31

    Bone as a sink of a number of long-lived radionuclides is a key organ for biokinetic model development and dosimetry studies. Development of a bone standard for the bone-seeking radionuclides is one of the most important tasks in ensuring quality control in bone-sample analysis and for providing a common basis for data comparison and evaluation. A bone ash standard under development at National Institute of Standards and Technology (NIST) for low-level radioactivity measurements provides a great analytical challenge to radiochemists because of its high calcium and phosphate content. In order to certify the concentration at about 1 mBq/g level radioactivity in the bone standard, analytical procedures using TRU-Apec extraction resin have been developed to overcome the difficulties caused by a high calcium phosphate matrix.

  15. Determination of strontium-90 from direct separation of yttrium-90 by solid phase extraction using DGA Resin for seawater monitoring.

    PubMed

    Tazoe, Hirofumi; Obata, Hajime; Yamagata, Takeyasu; Karube, Zin'ichi; Nagai, Hisao; Yamada, Masatoshi

    2016-05-15

    It is important for public safety to monitor strontium-90 in aquatic environments in the vicinity of nuclear related facilities. Strontium-90 concentrations in seawater exceeding the background level have been observed in accidents of nuclear facilities. However, the analytical procedure for measuring strontium-90 in seawater is highly demanding. Here we show a simple and high throughput analytical technique for the determination of strontium-90 in seawater samples using a direct yttrium-90 separation. The DGA Resin is used to determine the abundance of strontium-90 by detecting yttrium-90 decay (beta-emission) in secular equilibrium. The DGA Resin can selectively collect yttrium-90 and remove naturally occurring radionuclides such as (40)K, (210)Pb, (214)Bi, (238)U, and (232)Th and anthropogenic radionuclides such as (140)Ba, and (140)La. Through a sample separation procedure, a high chemical yield of yttrium-90 was achieved at 95.5±2.3%. The result of IAEA-443 certified seawater analysis (107.7±3.4mBqkg(-1)) was in good agreement with the certified value (110±5mBqkg(-1)). By developed method, we can finish analyzing 8 samples per day after achieving secular equilibrium, which is a reasonably fast throughput in actual seawater monitoring. By processing 3L of seawater sample and applying a counting time of 20h, minimum detectable activity can be as low as 1.5mBqkg(-1), which could be applied to monitoring for the contaminated marine environment. Reproducibility was found to be 3.4% according to 10 independent analyses of natural seawater samples from the vicinity of the Fukushima Daiichi Nuclear Power Plant in September 2013. PMID:26992514

  16. Adsorption characteristics of (-)-epigallocatechin gallate and caffeine in the extract of waste tea on macroporous adsorption resins functionalized with chloromethyl, amino, and phenylamino groups.

    PubMed

    Liu, Yongfeng; Bai, Qingqing; Lou, Song; Di, Duolong; Li, Jintian; Guo, Mei

    2012-02-15

    According to the Friedel-Crafts and amination reaction, a series of macroporous adsorption resins (MARs) with novel structures were synthesized and identified by the Brunauer-Emmett-Teller (BET) method and Fourier transform infrared (FTIR) spectra, and corresponding adsorption behaviors for (-)-epigallocatechin gallate (EGCG) and caffeine (CAF) extracted from waste tea were systemically investigated. Based on evaluation of adsorption kinetics, the kinetic data were well fitted by pseudo-second-order kinetics. Langmuir, Freundlich, Temkin-Pyzhev, and Dubinin-Radushkevich isotherms were selected to illustrate the adsorption process of EGCG and CAF on the MARs. Thermodynamic parameters were adopted to explain in-depth information of inherent energetic changes associated with the adsorption process. The effect of temperature on EGCG and CAF adsorption by D101-3 was further expounded. Van der Waals force, hydrogen bonding, and electrostatic interaction were the main driving forces for the adsorption of EGCG and CAF on the MARs. This study might provide a scientific reference point to aid the industrial large-scale separation and enrichment of EGCG from the extracts of waste tea using modified MARs. PMID:22243478

  17. Prevention of multiple low-dose streptozotocin (MLD-STZ) diabetes in mice by an extract from gum resin of Boswellia serrata (BE).

    PubMed

    Shehata, Ahmed M; Quintanilla-Fend, L; Bettio, Sabrina; Singh, C B; Ammon, H P T

    2011-09-15

    Type 1-diabetes is an autoimmune disease, where a chronic inflammatory process finally causes ?-cell death and insulin deficiency. Extracts from gum resin of Boswellia serrata (BE) have been shown to posses anti-inflammatory properties especially by targeting factors/mediators related to autoimmune diseases. Multiple low dose-streptozotocin (MLD-STZ) treatment is a method to induce diabetes in animals similar to Type 1 diabetes in humans. It was aimed to study whether or not a BE could prevent hyperglycemia, inflammation of pancreatic islets and increase of proinflammatory cytokines in the blood in MLD-STZ treated mice. In BK+/+ wild type mice, 5 days of daily treatment with 40 mg/kg STZ i.p. produced permanent increase of blood glucose, infiltration of lymphocytes into pancreatic islets (CD3-stain), apoptosis of periinsular cells (staining for activated caspase 3) after 10 days as well as shrinking of islet tissue after 35 days (H&E staining). This was associated with an increase of granulocyte colony stimulating factor (G-CSF), granulocyte/macrophage colony stimulating factor (GM-CSF) and proinflammatory cytokines (IL-1A, IL-1B, IL-2, IL-6, IFN-?, TNF-?) in the blood. Whereas BE alone did not affect blood glucose in non diabetic mice, in STZ treated mice simultaneous i.p. injection of 150 mg/kg of BE over 10 days prevented animals from increase of blood glucose levels. Histochemical studies showed, that i.p. injection of 150 mg/kg BE for 10 days starting with STZ treatment, avoided lymphocyte infiltration into islets, apoptosis of periinsular cells and shrinking of islet size 35 days after STZ. As far as the cytokines tested are concerned, there was a significant inhibition of the increase of G-CSF and GM-CSF. BE also significantly prevented the increase of IL-1A, IL-1B, IL-2, IL-6, IFN-? and TNF-?. It is concluded that extracts from the gum resin of Boswellia serrata prevent islet destruction and consequent hyperglycemia in an animal model of type 1 diabetes probably by inhibition of the production/action of cytokines related to induction of islet inflammation in an autoimmune process. PMID:21831620

  18. Glyoxal-Urea-Formaldehyde Molecularly Imprinted Resin as Pipette Tip Solid-Phase Extraction Adsorbent for Selective Screening of Organochlorine Pesticides in Spinach.

    PubMed

    Yang, Chen; Lv, Tianwei; Yan, Hongyuan; Wu, Gaochan; Li, Haonan

    2015-11-01

    A new kind of glyoxal-urea-formaldehyde molecularly imprinted resin (GUF-MIR) was synthesized by a glyoxal-urea-formaldehyde (GUF) gel imprinting method with 4,4'-dichlorobenzhydrol as a dummy template. The obtained GUF-MIR was characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FT-IR) and applied as a selective adsorbent of miniaturized pipet tip solid-phase extraction (PT-SPE) for the separation and extraction of three organochlorine pesticides (dicofol (DCF), dichlorodiphenyl dichloroethane (DDD), and tetradifon) in spinach samples. The proposed pretreatment procedures of spinach samples involved only 5.0 mg of GUF-MIR, 0.7 mL of MeOH-H2O (1:1, v/v) (washing solvent), and 0.6 mL of cyclohexane-ethyl acetate (9:1, v/v) (elution solvent). In comparison with other adsorbents (such as silica gel, C18, NH2-silica gel, and neutral alumina (Al2O3-N)), GUF-MIR showed higher adsorption and purification capacity for DCF, DDD, and tetradifon in aqueous solution. The average recoveries at three spiked levels ranged from 89.1% to 101.9% with relative standard deviations (RSDs) ≤ 7.1% (n = 3). The presented GUF-MIR-PT-SPE method combines the advantages of molecularly imprinted polymers (MIPs), GUF, and PT-SPE and can be used in polar solutions with high affinity and selectivity to the analytes in complex samples. PMID:26449689

  19. The Effect of Aloe Vera, Pomegranate Peel, Grape Seed Extract, Green Tea, and Sodium Ascorbate as Antioxidants on the Shear Bond Strength of Composite Resin to Home-bleached Enamel

    PubMed Central

    Sharafeddin, Farahnaz; Farshad, Farnaz

    2015-01-01

    Statement of the Problem Immediate application of bonding agent to home- bleached enamel leads to significant reduction in the shear bond strength of composite resin due to the residual oxygen. Different antioxidant agents may overcome this problem. Purpose This study aimed to assess the effect of different antioxidants on the shear bond strength of composite resin to home-bleached. Materials and Method Sixty extracted intact human incisors were embedded in cylindrical acrylic resin blocks (2.5×1.5 cm), with the coronal portion left out of the block. After bleaching the labial enamel surface with 15% carbamide peroxide, they were randomly divided into 6 groups (n=10). Before performing composite resin restoration by using a cylindrical Teflon mold (5×2 mm), each group was treated with one of the following antioxidants: 10% sodium ascorbate solution, 10% pomegranate peel solution, 10% grape seed extract, 5% green tea extract, and aloe vera leaf gel. One group was left untreated as the control. The shear bond strength of samples was tested under a universal testing machine (ZwickRoell Z020). The shear bond strength data were analyzed by one-way ANOVA and post hoc Tukey tests (p< 0.05). Results No significant difference existed between the control and experimental groups. Moreover, there was no statistically significant difference between the effects of different antioxidants on the shear bond strength of bleached enamel. Conclusion Different antioxidants used in this study had the same effect on the shear bond strength of home-bleached enamel, and none of them caused a statistically significant increase in its value. PMID:26636116

  20. Separation of vitexin-4″-O-glucoside and vitexin-2″-O-rhamnoside from hawthorn leaves extracts using macroporous resins.

    PubMed

    Li, Hongjuan; Liu, Ying; Jin, Haizhu; Liu, Sujing; Fang, Shengtao; Wang, Chunhua; Xia, Chuanhai

    2015-12-15

    Vitexin-4″-O-glucoside and vitexin-2″-O-rhamnoside are the major flavonoids of hawthorn leaves. In this work, the adsorption and desorption characteristics of vitexin-4″-O-glucoside and vitexin-2″-O-rhamnoside on seven macroporous resins were evaluated. Among the tested resins, the HPD-400 resin showed the best adsorption and desorption capacities. Adsorption isotherms were constructed for the HPD-400 resin and well fitted to Langmuir and Freundlich models. Dynamic adsorption and desorption tests were performed on column packed with the HPD-400 resin to optimize the chromatographic parameters. After one run treatment with the HPD-400 resin, the contents of vitexin-4″-O-glucoside and vitexin-2″-O-rhamnoside in the product were increased 8.44-fold and 8.43-fold from 0.720% and 2.63% to 6.08% and 22.2% with recovery yields of 79.1% and 81.2%, respectively. These results show that the developed method is a promising basis for the large-scale purification of vitexin-4″-O-glucoside and vitexin-2″-O-rhamnoside from hawthorn leaves and other plant materials. PMID:26562804

  1. Method of purifying neutral organophosphorus extractants

    SciTech Connect

    Horwitz, E. Philip; Gatrone, Ralph C.; Chiarizia, Renato

    1988-01-01

    A method for removing acidic contaminants from neutral mono and bifunctional organophosphorous extractants by contacting the extractant with a macroporous cation exchange resin in the H.sup.+ state followed by contact with a macroporous anion exchange resin in the OH.sup.- state, whereupon the resins take up the acidic contaminants from the extractant, purifying the extractant and improving its extraction capability.

  2. 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.

  3. 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.

  4. Determination of melamine in animal feed based on liquid chromatography tandem mass spectrometry analysis and dynamic microwave-assisted extraction coupled on-line with strong cation-exchange resin clean-up.

    PubMed

    Chen, Ligang; Zeng, Qinglei; Du, Xiaobo; Sun, Xin; Zhang, Xiaopan; Xu, Yang; Yu, Aimin; Zhang, Hanqi; Ding, Lan

    2009-11-01

    In this work, a new method was developed for the determination of melamine (MEL) in animal feed. The method was based on the on-line coupling of dynamic microwave-assisted extraction (DMAE) to strong cation-exchange (SCX) resin clean-up. The MEL was first extracted by 90% acidified methanol aqueous solution (v/v, pH = 3) under the action of microwave energy, and then the extract was cooled and passed through the SCX resin. Thus, the protonated MEL was retained on the resin through ion exchange interaction and the sample matrixes were washed out. Some obvious benefits were achieved, such as acceleration of analytical process, together with reduction in manual handling, risk of contamination, loss of analyte, and sample consumption. Finally, the analyte was separated by a liquid chromatograph with a SCX analytical column, and then identified and quantitatived by a tandem mass spectrometry with positive ionization mode and multiple-reaction monitoring. The DMAE parameters were optimized by the Box-Behnken design. The linearity of quantification obtained by analyzing matrix-matched standards is in the range of 50-5,000 ng g(-1). The limit of detection and limit of quantification obtained are 12.3 and 41.0 ng g(-1), respectively. The mean intra- and inter-day precisions expressed as relative standard deviations with three fortified levels (50, 250, and 500 ng g(-1)) are 5.1% and 7.3%, respectively, and the recoveries of MEL are in the range of 76.1-93.5%. The proposed method was successfully applied to determine MEL in different animal feeds obtained from the local market. MEL was detectable with the contents of 279, 136, and 742 ng g(-1) in three samples. PMID:19756536

  5. Resin hybrid composite laminates

    SciTech Connect

    Bhatnagar, A.

    1986-01-01

    Hybrid composites are generally referred to as the materials that combine two or more fibers in a suitable binding resin. Resin hybrid composites described in this paper utilize two or more resins with a suitable reinforcement. The resins are rigid resin and flexible resins. The elongation of the rigid resin is less than 2% and elongation of the flexible resins are varied between 25% to 100% by blending a very flexible resin with the rigid resin. Test laminates are fabricated by using either glass, carbon or aramid reinforcement in a layered sequence. This produces rigid-flexible-rigid and flexible-rigid-flexible laminates. These laminates are tested for impact, compression, flexural and inter-laminar strengths. Results show that the resin hybriding provides a wide choice of mechanical properties to the composite industry.

  6. Preconcentration of trace metals from sea water with 7-dodecenyl-8-quinolinol impregnated macroporous resin

    SciTech Connect

    Isshiki, K.; Tsuji, F.; Kuwamoto, T.; Nakayama, E.

    1987-10-15

    7-Dodecenyl-8-quinolinol (DDQ) impregnated XAD-4 resin (DDQ resin) was prepared, and its extraction behavior was studied and compared with solvent extraction with DDQ for Aq, Al, Bi, Cd, Cu, Fe, Ga, Mn, Ni, Pb, and Ti. The results demonstrate that the DDQ resin is effective in the preconcentration of those metals from sea water. The column extraction method using the DDQ resin was applied to sea water analysis with satisfactory results being obtained.

  7. 21 CFR 177.1555 - Polyarylate resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... finished polyarylate resins in sheet form at least 0.5 millimeter (0.020 inch) thick, when extracted with water at 121 °C (250 °F) for 2 hours, shall yield total nonvolatile extractives not to exceed...

  8. Process for preparing phenolic formaldehyde resole resin products derived from fractionated fast-pyrolysis oils

    DOEpatents

    Chum, Helena L.; Kreibich, Roland E.

    1992-01-01

    A process for preparing phenol-formaldehyde resole resins and adhesive compositions in which portions of the phenol normally contained in said resins are replaced by a phenol/neutral fractions extract obtained from fractionating fast-pyrolysis oils.

  9. 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

  10. Guayule resin detection and influence on guayule rubber

    Technology Transfer Automated Retrieval System (TEKTRAN)

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

  11. Resin collection and social immunity in honey bees

    Technology Transfer Automated Retrieval System (TEKTRAN)

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

  12. 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

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

    PubMed

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

    2012-08-21

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

  14. 21 CFR 177.2415 - Poly(aryletherketone) resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... of hydroquinone and 4,4′-difluorobenzophenone, and have a minimum weight-average molecular weight of... percent by weight as a residual solvent in the finished basic resin. (c) Extractive limitations....

  15. Extract of gum resins of Boswellia serrata L. inhibits lipopolysaccharide induced nitric oxide production in rat macrophages along with hypolipidemic property.

    PubMed

    Pandey, Ravi S; Singh, Birendra K; Tripathi, Yamini B

    2005-06-01

    Boswellia serrata, Linn F (Burseraceae) is commonly used in Indian system of medicine (Ayurvedic) as an anti-inflammatory, analgesic, anti-arthritic and anti-proliferative agent. This study was planned to investigate the water-soluble fraction of the oleoresin gum of Boswellia serrata (BS extract) on lipopolysaccharide (LPS) induced nitric oxide (NO) production by macrophages under in vivo and in vitro conditions. In the previous condition, rats were fed on atherogenic diet (2.5% cholesterol, 1% cholic acid, 15.7 % saturated fat) along with the BS extract for 90 days. Blood was collected for lipid profile and toxicological safety parameters. Peritoneal macrophages were isolated and cultured to see the LPS induced NO production. Under in vivo experiment, BS extract significantly reduced serum total cholesterol (38-48 %), increased serum high-density lipoprotein- cholesterol (HDL-cholesterol, 22-30%). Under in vitro experiments with thioglycolate activated macrophages, it inhibited LPS induced (NO) production with IC 50 value at 662 ng /ml. Further, this fraction, in the dose of 15 mg/100 g body wt for 90 days, did not show any increase in serum glutamate-pyruvate transaminase (SGPT) and blood urea, in normal control animals. However, it significantly reversed the raised SGPT and blood urea in the atherogenic diet-fed animals. Transverse section of liver and kidney also supported its protective effect. Thus it may be concluded that water extract of Boswellia serrata possesses strong hypocholesterolemic property along with increase in serum HDL. It inhibits the LPS induced NO production by the activated rat peritoneal macrophages and show hepato-protective and reno-protective property. PMID:15991575

  16. 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.

  17. 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)

  18. Development of resins for composites by resin transfer molding

    NASA Technical Reports Server (NTRS)

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

    1991-01-01

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

  19. Biocompatibility of composite resins

    PubMed Central

    Mousavinasab, Sayed Mostafa

    2011-01-01

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

  20. 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.

  1. 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.

  2. 21 CFR 177.1632 - Poly(phenyl-enetereph-thala-mide) resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...(phenyleneterephthalamide) resin fibers and yarns may contain optional adjuvant substances required in their preparation and... extractables not exceeding 0.5 percent by weight of the sample. (2) Poly(phenyleneterephthalamide) resins in... extractables not exceeding 0.65 percent by weight of the sample. (d) Conditions of use. (1)...

  3. 21 CFR 177.1632 - Poly(phenyl-enetereph-thala-mide) resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...(phenyleneterephthalamide) resin fibers and yarns may contain optional adjuvant substances required in their preparation and... extractables not exceeding 0.5 percent by weight of the sample. (2) Poly(phenyleneterephthalamide) resins in... extractables not exceeding 0.65 percent by weight of the sample. (d) Conditions of use. (1)...

  4. 21 CFR 177.1632 - Poly (phenyl-enetereph-thala-mide) resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...(phenyleneterephthalamide) resin fibers and yarns may contain optional adjuvant substances required in their preparation and... extractables not exceeding 0.5 percent by weight of the sample. (2) Poly(phenyleneterephthalamide) resins in... extractables not exceeding 0.65 percent by weight of the sample. (d) Conditions of use. (1)...

  5. Phenolic Resin for Refractories

    NASA Astrophysics Data System (ADS)

    Irie, Shunsuke; Rappolt, James

    Refractories are used in furnaces and boilers that process steel, cement, or glass as well as incinerators that operate at high temperatures. A variety of binders is used when refractories are manufactured. In this chapter, the use of phenolic resin as a binder for refractories is described. There are several factors that support the use of phenolic resins in comparison to other refractory binders. These include the following: 1. Both adhesion and green body strength are high.

  6. 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.

  7. Acetylene terminated matrix resins

    NASA Technical Reports Server (NTRS)

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

    1985-01-01

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

  8. Quantification and Purification of Mulberry Anthocyanins With Macroporous Resins

    PubMed Central

    Liu, Xueming

    2004-01-01

    Total anthocyanins in different cultivars of mulberry were measured and a process for the industrial preparation of mulberry anthocyanins as a natural food colorant was studied. In 31 cultivars of mulberry, the total anthocyanins, calculated as cyanidin 3-glucoside, ranged from 147.68 to 2725.46?mg/L juice. Extracting and purifying with macroporous resins was found to be an efficient potential method for the industrial production of mulberry anthocyanins as a food colorant. Of six resins tested, X-5 demonstrated the best adsorbent capability for mulberry anthocyanins (91?mg/mL resin). The adsorption capacity of resins increased with the surface area and the pore radius. Residual mulberry fruit juice after extraction of pigment retained most of its nutrients, except for anthocyanins, and may provide a substrate for further processing. PMID:15577197

  9. Quantification and Purification of Mulberry Anthocyanins with Macroporous Resins.

    PubMed

    Liu, Xueming; Xiao, Gengsheng; Chen, Weidong; Xu, Yujuan; Wu, Jijun

    2004-01-01

    Total anthocyanins in different cultivars of mulberry were measured and a process for the industrial preparation of mulberry anthocyanins as a natural food colorant was studied. In 31 cultivars of mulberry, the total anthocyanins, calculated as cyanidin 3-glucoside, ranged from $147.68$ to $2725.46$ mg/L juice. Extracting and purifying with macroporous resins was found to be an efficient potential method for the industrial production of mulberry anthocyanins as a food colorant. Of six resins tested, X-5 demonstrated the best adsorbent capability for mulberry anthocyanins (91 mg/mL resin). The adsorption capacity of resins increased with the surface area and the pore radius. Residual mulberry fruit juice after extraction of pigment retained most of its nutrients, except for anthocyanins, and may provide a substrate for further processing. PMID:15577197

  10. Branched polymeric media: perchlorate-selective resins from hyperbranched polyethyleneimine.

    PubMed

    Chen, Dennis P; Yu, Changjun; Chang, Ching-Yu; Wan, Yanjian; Frechet, Jean M J; Goddard, William A; Diallo, Mamadou S

    2012-10-01

    Perchlorate (ClO(4)(-)) is a persistent contaminant found in drinking groundwater sources in the United States. Ion exchange (IX) with selective and disposable resins based on cross-linked styrene divinylbenzene (STY-DVB) beads is currently the most commonly utilized process for removing low concentrations of ClO(4)(-) (10-100 ppb) from contaminated drinking water sources. However, due to the low exchange capacity of perchlorate-selective STY-DVB resins (∼0.5-0.8 eq/L), the overall cost becomes prohibitive when treating groundwater with higher concentration of ClO(4)(-) (e.g., 100-1000 ppb). In this article, we describe a new perchlorate-selective resin with high exchange capacity. This new resin was prepared by alkylation of branched polyethyleneimine (PEI) beads obtained from an inverse suspension polymerization process. Batch and column studies show that our new PEI resin with mixed hexyl/ethyl quaternary ammonium chloride exchange sites can selectively extract trace amounts of ClO(4)(-) from a makeup groundwater (to below detection limit) in the presence of competing ions. In addition, this resin has a strong-base exchange capacity of 1.4 eq/L, which is 1.75-2.33 times larger than those of commercial perchlorate-selective STY-DVB resins. The overall results of our studies suggest that branched PEI beads provide versatile and promising building blocks for the preparation of perchlorate-selective resins with high exchange capacity. PMID:22950356

  11. Resin Infiltration into Differentially Extended Experimental Carious Lesions

    PubMed Central

    Arnold, Wolfgang H; Bachstaedter, Lena; Benz, Korbinian; Naumova, Ella A

    2014-01-01

    Resin infiltration of initial caries lesions is a novel method of caries therapy. However, it has some limitations. Therefore, further experimental studies are needed to improve resin infiltration. It was the aim of this investigation to study resin infiltra-tion into different experimental carious lesions. Caries-free extracted human molars and premolars were demineralized for 3, 6, 9 and 12 days and infiltrated with resin. Prior to infiltration, the teeth were incubated with sodium fluorescein. After em-bedding, serial sections were cut through the experimental lesions, and the penetration of the resin was measured with fluo-rescence microscopy. Two infiltrated teeth from each time interval were not embedded and cut. Infiltration of the resin was then studied with EDS element analysis. The results showed that with increasing demineralization time, the lesion expansion was also increasing, and the resin infiltration was always almost complete. From these results it can be concluded that artifi-cial standardized caries-like lesions are suitable for experimental studies of resin infiltration. PMID:26019729

  12. Effects of Guayule Resin on Termite Feeding Activity

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Guayule, a desert adapted plant, yields hypoallergenic rubber that is used primarily by the medical profession for rubber gloves, catheters, etc. Terpene resin, a co-product from guayule that can be extracted prior to rubber extraction, has been found to have termiticidal properties. As such, this r...

  13. 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.

  14. Refining of fossil resin flotation concentrate from Western coal. Second quarterly final report, April 1, 1993--June 30, 1993

    SciTech Connect

    Jensen, G.F.; Miller, J.D.

    1993-07-10

    Ultimate analysis was conducted for the fossil resin concentrate and results obtained are given in Table 2. Based on these results and other results from spectroscopic analysis it appears that the fossil resin from the Wasatch Plateau coal field consists mainly of aliphatic components and partially aromatized multicyclic terpenoids with a few oxygen functional groups. As compared with the parent high volatile bituminous coal, the resin has higher hydrogen and carbon content, low oxygen, nitrogen, and sulfur contents, and relatively low aromaticity. The values of the acid number and iodine number indicate that the fossil resins from the Wasatch Plateau coal field contain only a modest amount of oxygen functional groups and unsaturated carbon-carbon double-bonds in their molecular structures. Fossil resin is a complex mixture of sesquiterpenoids and the solubility of these resin compounds depends on the type of solvent used. The determination of the extractable resin content in the resin concentrate by different solvents provides an important control variable for selective solvent refining and purification. The data generated during preliminary solvent extraction tests are especially important for process design, control of the refined resin quality and prediction of the refined resin products. In this work, the extractable resin content was determined for each size fraction with four solvents: ethyl acetate (ACS grade), hexanes (ACS grade), heptane (98%, assay grade), and toluene (ACS grade). The extraction tests were conducted in TX-6 Soxhlet extraction units. Results are given in Table 5.

  15. Determination of Human-Health Pharmaceuticals in Filtered Water by Chemically Modified Styrene-Divinylbenzene Resin-Based Solid-Phase Extraction and High-Performance Liquid Chromatography/Mass Spectrometry

    USGS Publications Warehouse

    Furlong, Edward T.; Werner, Stephen L.; Anderson, Bruce D.; Cahill, Jeffery D.

    2008-01-01

    In 1999, the Methods Research and Development Program of the U.S. Geological Survey National Water Quality Laboratory began the process of developing a method designed to identify and quantify human-health pharmaceuticals in four filtered water-sample types: reagent water, ground water, surface water minimally affected by human contributions, and surface water that contains a substantial fraction of treated wastewater. Compounds derived from human pharmaceutical and personal-care product use, which enter the environment through wastewater discharge, are a newly emerging area of concern; this method was intended to fulfill the need for a highly sensitive and highly selective means to identify and quantify 14 commonly used human pharmaceuticals in filtered-water samples. The concentrations of 12 pharmaceuticals are reported without qualification; the concentrations of two pharmaceuticals are reported as estimates because long-term reagent-spike sample recoveries fall below acceptance criteria for reporting concentrations without qualification. The method uses a chemically modified styrene-divinylbenzene resin-based solid-phase extraction (SPE) cartridge for analyte isolation and concentration. For analyte detection and quantitation, an instrumental method was developed that used a high-performance liquid chromatography/mass spectrometry (HPLC/MS) system to separate the pharmaceuticals of interest from each other and coextracted material. Immediately following separation, the pharmaceuticals are ionized by electrospray ionization operated in the positive mode, and the positive ions produced are detected, identified, and quantified using a quadrupole mass spectrometer. In this method, 1-liter water samples are first filtered, either in the field or in the laboratory, using a 0.7-micrometer (um) nominal pore size glass-fiber filter to remove suspended solids. The filtered samples then are passed through cleaned and conditioned SPE cartridges at a rate of about 15 milliliters per minute. Excess water is eliminated from the cartridge sorbent bed by passing air through the cartridges, and the analytes retained on the SPE bed are eluted from the cartridge sequentially, first with methanol, followed by acidified methanol, and combined in collection tubes. This sample extract then is reduced from about 10 milliliters (mL) to about 0.1 mL (or 100 microliters) under a stream of purified nitrogen gas with the collection tubes in a heated (40 degrees C) water bath. The reduced extracts then are fortified with an internal standard solution (when using internal standard quantitation), brought to a final volume of 1 mL with an aqueous ammonium formate buffer solution, and filtered through a 0.2-um Teflon syringe filter as they are transferred into vials for instrumental analysis. Instrumental analysis by the HPLC/MS procedure permits determination of individual pharmaceutical concentrations from 0.005 to 1.0 microgram per liter, based on the lowest and the highest calibration standards routinely used. The reporting levels for this method are compound dependent, and have been experimentally determined based on the precision of quantitation of compounds from eight fortified organic-free water samples in single-operator experiments. The method detection limits and interim reporting levels for the compounds determined by this method were calculated from recoveries of the pharmaceuticals from reagent-water samples amended at 0.05 microgram per liter, and ranged between 0.0069 and 0.0142 microgram per liter, and 0.015 and 0.10 microgram per liter, respectively. Concentrations for 12 compounds are reported without qualification, and for two compounds are reported as qualified estimates. After initial development, the method was applied to more than 1,800 surface-, ground-, and wastewater samples from 2002 to 2005 and documented in a number of published studies. This research application of the method provided the opportunity to collect a l

  16. Method for removing contaminants from plastic resin

    DOEpatents

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

    2008-12-09

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

  17. Absolute stereostructures of polypodane-type triterpenes, myrrhanol A and myrrhanone A, from guggul-gum resin (the resin of Balsamodendron mukul).

    PubMed

    Matsuda, Hisashi; Morikawa, Toshio; Ando, Shin; Oominami, Hideo; Murakami, Toshiyuki; Kimura, Ikuko; Yoshikawa, Masayuki

    2004-10-01

    Two new polypodane-type triterpenes, myrrhanol A and myrrhanone A, were isolated from the 50% aqueous methanolic extract of guggul-gum resin [the resin of Balsamodendron (=Commiphora) mukul HOOK]. The structures of the new constituents, including their absolute configurations, were determined on the basis of chemical and physicochemical evidence. PMID:15467235

  18. 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.

  19. Multidrug resistance-reversal effects of resin glycosides from Dichondra repens.

    PubMed

    Song, Wei-Bin; Wang, Wen-Qiong; Zhang, Shu-Wei; Xuan, Li-Jiang

    2015-02-15

    Investigation of hydrophobic extract of Dichondra repens (Convolvulaceae) led to the isolation of three new resin glycosides dichondrins A-C (1-3), and three known resin glycosides cus-1, cus-2, and cuse 3. All the isolated resin glycosides with an acyclic core were evaluated for their multidrug resistance reversal activities, and the combined use of these compounds at a concentration of 25μM increased the cytotoxicity of vincristine by 1.03-1.78-fold. PMID:25597010

  20. Nontoxic Resins Advance Aerospace Manufacturing

    NASA Technical Reports Server (NTRS)

    2009-01-01

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

  1. EP-toxicity testing of mercury removal resin grout

    SciTech Connect

    Mersman, K.E.

    1984-07-18

    To determine which category a waste will fit into, the EPA requires a classification test. The test, EP-toxicity, consists of a physical integrity test followed by an extraction. For the case of the mercury removal resin grout, the mercury concentration in the extract cannot exceed 0.2 mg/L if the waste is to be classified as ``solid waste.`` Otherwise, the waste is classified as ``hazardous.`` Simulated process solutions were used to load the mercury removal resin. The resin was solidified with the addition of cement and water using a formulation based on grout formulations typically used to solidify power reactor ion exchange resins. Envirodyne Engineers of St. Louis, Missouri, an EPA sanctioned laboratory, performed the EP-toxicity test for the two samples. One sample was a blank which was made with unloaded resin. For the formulation tested, the EP-toxicity test results showed that the mercury removal resin grout does not fit into the ``hazardous waste`` category.

  2. Flame Retardant Epoxy Resins

    NASA Technical Reports Server (NTRS)

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

    2004-01-01

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

  3. 40 CFR 414.40 - Applicability; description of the thermoplastic resins subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...-Maleic Anhydride Resins *Unsaturated Polyester Resins *Vinyl Toluene Resins *Vinyl Toluene-Acrylate... *Polycarbonates *Polyester Resins *Polyester Resins, Polybutylene Terephthalate *Polyester Resins,...

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

    SciTech Connect

    Serkiz, S.M.

    2000-09-05

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

  5. System for removing contaminants from plastic resin

    DOEpatents

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

    2010-11-23

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

  6. Color stability of composite resins.

    PubMed

    Chang, Y G; Swartz, M L; Moore, B K; Cochran, M A; Lund, M R

    1990-10-01

    The color stability of seven visible light-cured and three chemically-cured composite resins was investigated while being subjected to UV light irradiation and storage in an aqueous environment at elevated temperatures. Color shift was evaluated visually and by colorimetric measurements. Significant correlation was found between visual scoring and colorimetric readings. When subjected to UV light, a wide deviation in color change existed from brand to brand in photocured composite resins. The color shift of chemically-cured composite resins was less than but fell within the range of photocured composite resins. When stored in water at elevated temperatures, photocured resins exhibited better color stability than the chemically-cured composite resins. PMID:2243370

  7. 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.

  8. Vitrification of ion exchange resins

    DOEpatents

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

    2001-01-01

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

  9. Phosphorus-containing bisimide resins

    NASA Technical Reports Server (NTRS)

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

    1981-01-01

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

  10. Refining of fossil resin flotation concentrate from Western coal. Third quarterly final report, July 1, 1993--September 30, 1993

    SciTech Connect

    Jensen, G.F.; Miller, J.D.

    1993-10-04

    Summary of Batch Extraction Experiments: (1) Resin extraction rate is not significantly affected by agitation intensity and low agitation should be suitable for the continuous extraction process; (2) The effect of resin particle size on the extraction rate and yield is obvious. Because of the fine size of the composite resin concentrate (80% minus 200 mesh), the extraction reaction occurs in reasonable times and process design conditions can be established accordingly; (3) The effect of temperature on the rate and yield of the extraction process is found to be very significant. Higher temperatures (about 60{degree}C) should be considered for the continuous extraction circuit; (4) The effect of solids concentration on the extraction rate is moderate. As concluded from our characterization study, it is known that fossil resin is mainly composed of aliphatic components, partially aromatized multicyclic compounds with a small number of oxygen functional groups. The solvent, heptane, is also a nonpolar aliphatic compound. It is expected that no chemical reaction will occur in such an extraction process at low temperature (0--90{degree}C). The main interaction between resin and heptane is expected to be the van-der-Waals-forces of interaction associated with solvation phenomena. In this regard, the resin extraction rate should be largely independent of agitation intensity at room temperature, low solids concentration and moderate agitation. The initial extraction rate was found to be inversely proportional to the initial particle diameter. The temperature has significant effect on extraction rate and the activation energy for resin extraction by heptane was found to be 15.5 kcal/mole. The resin extraction kinetics can be expressed by the equation given.

  11. Imide modified epoxy matrix resins

    NASA Technical Reports Server (NTRS)

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

    1981-01-01

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

  12. Amalgam vs. composite resin: 1998.

    PubMed

    Christensen, G J

    1998-12-01

    Class II resin restorations have been evolving in American dentistry for 30 years, but the concept has had significant difficulty being accepted because of stigma attached to early generations of composites. Currently available composite resins for posterior tooth restorations have physical characteristics justifying their use. Techniques for Class II resin placement have improved significantly, and mastery of them is within the ability of both dentists and dental students. Although composite resin materials and techniques present clinical challenges, so do amalgam materials and techniques. It is time to accept Class II resin restorations, improve dentist and student education about their use, increase acceptance by third-party organizations and various approving groups, and bring this concept into the mainstream of U.S. dentistry. PMID:9854929

  13. Synthesis and application of a new functionalized resin for use in an on-line, solid phase extraction system for the determination of trace elements in waters and reference cereal materials by flame atomic absorption spectrometry.

    PubMed

    Karada?, Cennet; Turhan, Onur; Kara, Derya

    2013-11-15

    The synthesis and characterization of the resin Amberlite XAD-4 functionalized with 2,6-pyridinedicarboxaldehyde and its application in an on-line system for the preconcentration of cadmium, cobalt, copper, lead and manganese prior to determination using flame atomic absorption spectrometry (FAAS) is proposed. Metal ions retained on the modified resin were eluted using 1.0 mol L(-1) HNO3 solution and aspirated directly to the nebulizer-burner system of a FAAS instrument using a flow injection system. Detection limits (3?) were determined to be 0.13 ?g L(-1) for Cd, 0.29 ?g L(-1) for Cu, 0.23 ?g L(-1) for Mn, 0.58 ?g L(-1) for Co and 2.19 ?g L(-1) for Pb using a 10 mL of water sample loading volume. The limits of detection would be 100 times higher with units of ?g kg(-1) for the solid samples in which their dilution ratios as (volume/weight) were 100. Enrichment factors ranged from 23.6 to 28.9 (for Co and Mn, respectively). The proposed method was successfully applied to determination of the analytes in natural water samples and certified reference materials. PMID:23790831

  14. Cobalt dicarbollide containing polymer resins for cesium and strontium uptake

    SciTech Connect

    Steckle, W.P. Jr.; Duke, J.R. Jr.; Jorgensen, B.S.

    1994-04-01

    Cobalt(III) dicarbollide [(C{sub 2}B{sub 9}H{sub 11}){sub 2}Co]{sup {minus}} (CB{sub 2}) is being investigated for Cs and Sr extraction from nuclear waste. Because organic solvents should be avoided, bonding of CB{sub 2} to resins were investigated. CB{sub 2} was successfully covalently bonded to polystyrene and polybenzimidazole resins. Tetrahydrofuran was the most efficient solvent for grafting. Analysis is being performed, and separation coefficients are also being determined. 3 figs, 8 refs.

  15. Refining of fossil resin flotation concentrate from western coal. Final report

    SciTech Connect

    Jensen, G.F.; Miller, J.D.

    1995-02-16

    During the past several years, significant research efforts have been made to develop process technology for the selective flotation of fossil resin from western coals. As a result of these efforts, several new flotation technologies have been developed. Operation of a proof-of-concept continuous flotation circuit showed the selective flotation process to be sufficiently profitable to justify the development of a fossil resin industry. However, little attention has been given to the refining of the fossil resin flotation concentrate although solvent refining is a critical step for the fossil resin to become a marketable product. In view of this situation, DOE funded this two-year project to evaluate the following aspects of the fossil resin refining technology: 1) Characterization of the fossil resin flotation concentrate and its refined products; 2) Kinetics of fossil resin extraction; 3) Effects of operating variables on solvent extraction; 4) Extraction solvents; 5) Proof-of-concept continuous refining tests; and 6) Technical and economic analysis. The results from this research effort have led to the following conclusions: Hexane- or heptane-refined fossil resin has a light-yellow color, a melting point of 140 - 142{degrees}C, a density of 1.034 gram/cm, and good solubility in nonpolar solvents. Among the four solvents evaluated (hexane, heptane, toluene and ethyl acetate), hexane is the most appropriate solvent based on overall technical and economic considerations. Batch extraction tests and kinetic studies suggest that the main interaction between the resin and the solvent is expected to be the forces associated with solvation phenomena. Temperature has the most significant effect on extraction rate. With hexane as the solvent, a recovery of 90% cam be achieved at 50{degrees}C and 10% solids concentration with moderate agitation for 1 hour.

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

    PubMed Central

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

    2015-01-01

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

  17. Significance of wood extractives for wood bonding.

    PubMed

    Roffael, Edmone

    2016-02-01

    Wood contains primary extractives, which are present in all woods, and secondary extractives, which are confined in certain wood species. Extractives in wood play a major role in wood-bonding processes, as they can contribute to or determine the bonding relevant properties of wood such as acidity and wettability. Therefore, extractives play an immanent role in bonding of wood chips and wood fibres with common synthetic adhesives such as urea-formaldehyde-resins (UF-resins) and phenol-formaldehyde-resins (PF-resins). Extractives of high acidity accelerate the curing of acid curing UF-resins and decelerate bonding with alkaline hardening PF-resins. Water-soluble extractives like free sugars are detrimental for bonding of wood with cement. Polyphenolic extractives (tannins) can be used as a binder in the wood-based industry. Additionally, extractives in wood can react with formaldehyde and reduce the formaldehyde emission of wood-based panels. Moreover, some wood extractives are volatile organic compounds (VOC) and insofar also relevant to the emission of VOC from wood and wood-based panels. PMID:26685670

  18. Chromatography resin support

    DOEpatents

    Dobos, James G.

    2002-01-01

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

  19. 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.

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

    PubMed

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

    1999-01-01

    Negative effects of rapid, high-intensity resin curing have been predicted for both argon lasers and plasma-arc curing lights. To address these questions, six different resin restorative materials were cured with 14 different resin curing lights representing differences in intensities ranging from 400 mW/cm2 to 1,900 mW/cm2; delivery modes using constant, ramped, and stepped methods; cure times ranging from 1 second to 40 seconds; and spot sizes of 6.7 mm to 10.9 mm. Two lasers, five plasma-arc lights, and seven halogen lights were used. Shrinkage, modulus, heat generation, strain, and physical changes on the teeth and resins during strain testing were documented. Results showed effects associated with lights were not statistically significant, but resin formulation was highly significant. Microfill resins had the least shrinkage and the lowest modulus. An autocure resin had shrinkage and modulus as high as or higher than the light-cured hybrid resins. Lasers and plasma-arc lights produced the highest heat increases on the surface (up to 21 degrees C) and within the resin restorations (up to 14 degrees C), and the halogen lights produced the most heat within the pulp chamber (up to 2 degrees C). Strain within the tooth was least with Heliomolar and greatest with Z100 Restorative and BISFIL II autocure resin. Clinical effects of strain relief were evident as white lines at the tooth-resin interface and cracks in enamel adjacent to the margins. This work implicates resin formulation, rather than light type or curing mode, as the important factor in polymerization problems. Lower light intensity and use of ramped and stepped curing modes did not provide significant lowering of shrinkage, modulus, or strain, and did not prevent enamel cracking adjacent to margins and formation of "white line" defects at the margins. Until materials with lower shrinkage and modulus are available, use of low-viscosity surface sealants as a final step in resin placement is suggested to seal defects. PMID:11908396

  1. Grafted methylenediphosphonate ion exchange resins

    DOEpatents

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

    1997-01-01

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

  2. Grafted methylenediphosphonate ion exchange resins

    DOEpatents

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

    1998-01-27

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

  3. 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.

  4. 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.

  5. 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.

  6. 21 CFR 177.1680 - Polyurethane resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyurethane resins. 177.1680 Section 177.1680... Contact Surfaces § 177.1680 Polyurethane resins. The polyurethane resins identified in paragraph (a) of..., polyurethane resins are those produced when one or more of the isocyanates listed in paragraph (a)(1) of...

  7. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

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

  8. 21 CFR 177.1580 - Polycarbonate resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polycarbonate resins. 177.1580 Section 177.1580... Contact Surfaces § 177.1580 Polycarbonate resins. Polycarbonate resins may be safely used as articles or...) Polycarbonate resins are polyesters produced by: (1) The condensation of 4,4′-iso-propylidenediphenol...

  9. 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.

  10. Liquid chromatographic extraction medium

    DOEpatents

    Horwitz, E. Philip (Naperville, IL); Dietz, Mark L. (Evanston, IL)

    1994-01-01

    A method and apparatus for extracting strontium and technetium values from biological, industrial and environmental sample solutions using a chromatographic column is described. An extractant medium for the column is prepared by generating a solution of a diluent containing a Crown ether and dispersing the solution on a resin substrate material. The sample solution is highly acidic and is introduced directed to the chromatographic column and strontium or technetium is eluted using deionized water.

  11. Liquid chromatographic extraction medium

    DOEpatents

    Horwitz, E.P.; Dietz, M.L.

    1994-09-13

    A method and apparatus are disclosed for extracting strontium and technetium values from biological, industrial and environmental sample solutions using a chromatographic column. An extractant medium for the column is prepared by generating a solution of a diluent containing a Crown ether and dispersing the solution on a resin substrate material. The sample solution is highly acidic and is introduced directed to the chromatographic column and strontium or technetium is eluted using deionized water. 1 fig.

  12. Resole resin products derived from fractionated organic and aqueous condensates made by fast-pyrolysis of biomass materials

    DOEpatents

    Chum, H.L.; Black, S.K.; Diebold, J.P.; Kreibich, R.E.

    1993-08-10

    A process for preparing phenol-formaldehyde resole resins by fractionating organic and aqueous condensates made by fast-pyrolysis of biomass materials while using a carrier gas to move feed into a reactor to produce phenolic-containing/neutrals in which portions of the phenol normally contained in said resins are replaced by a phenolic/neutral fractions extract obtained by fractionation.

  13. Resole resin products derived from fractionated organic and aqueous condensates made by fast-pyrolysis of biomass materials

    DOEpatents

    Chum, Helena L.; Black, Stuart K.; Diebold, James P.; Kreibich, Roland E.

    1993-01-01

    A process for preparing phenol-formaldehyde resole resins by fractionating organic and aqueous condensates made by fast-pyrolysis of biomass materials while using a carrier gas to move feed into a reactor to produce phenolic-containing/neutrals in which portions of the phenol normally contained in said resins are replaced by a phenolic/neutral fractions extract obtained by fractionation.

  14. Regenerating Water-Sterilizing Resins

    NASA Technical Reports Server (NTRS)

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

    1982-01-01

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

  15. Liquid monobenzoxazine based resin system

    SciTech Connect

    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.

  16. 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).

  17. Regional measurement of resin-dentin bonding as an array.

    PubMed

    Shono, Y; Ogawa, T; Terashita, M; Carvalho, R M; Pashley, E L; Pashley, D H

    1999-02-01

    During the development of the microtensile bond-testing method, large variations in bond strengths were noted among serial sections. The reason for these variations is unknown. The purpose of this work was to determine the consistency of resin-dentin bond strengths across the occlusal surface of coronal dentin by dividing composite resin buildups into an array of 1x1 mm beams, the top half consisting of composite resin, and the bottom half consisting of dentin. Extracted human third molars had the occlusal enamel removed as a single section by means of a diamond saw. Resin composite buildups were made after the dentin was bonded with either One-Step or MacBond. After being stored in 37 degrees C water for 1 day, the teeth were vertically sectioned at 1-mm increments into slabs of bonded teeth. Each slab was further subdivided by vertical sections into 1x1x8 mm beams. Each beam was assigned an x-y coordinate and tested for tensile bond strength. Two different clinicians (A and B) performed the same procedures using One-Step in a parallel study. Using One-Step, clinician A obtained a large number of zero bonds in superficial dentin but fewer in deep dentin. This resulted in a very large standard deviation in bond strengths (mean +/- SD of 22+/-20 MPa in superficial dentin and 27+/-14 MPa in deep dentin). Clinician B obtained much higher (p<0.001) and more uniform bond strengths with One-Step (56+/-13 MPa in superficial dentin and 57+/-12 MPa in deep dentin). With MacBond, there were no zero bonds and hence less variation, with a mean of 41+/-13 MPa in superficial dentin and 27+/-12 MPa (x +/- SD) in deep dentin. When pairs of Z100 resin composite cylinders were bonded together with One-Step and then sectioned into an array, there was little variation in regional bond strength (37 +/-1 MPa). Dividing bonded resin composite buildups into an array of 20 to 30 1x1x8 mm beams allows for the evaluation of uniformity of resin-dentin bonds. The method used in this study detected local regional differences in resin-dentin bond strengths. The largest differences were shown to be related to technique rather than to material. The results indicate that resin-dentin bonds may not be as homogenous as was previously thought. PMID:10029469

  18. Direct analysis of oligomeric tackifying resins in rubber compounds by automatic thermal desorption gas chromatography/mass spectrometry

    PubMed

    Kim

    1999-01-01

    Two analytical methods, automatic thermal desorption gas chromatography/mass spectrometry (ATD-GC/MS) and pyrolysis gas chromatography/mass spectrometry (Py-GC/MS), were applied as direct methods for the analysis of oligomeric tackifying resins in a vulcanized rubber. The ATD-GC/MS method, based on discontinuous volatile extraction, was found to be an effective means for direct analysis of the oligomeric tackifying resins contained in a vulcanized rubber. The oligomeric tackifying resins, such as t-octylphenolformaldehyde (TOPF) resin, rosin-modified terpene resin, and cashew resin, could be directly analyzed in vulcanized rubber by ATD-GC/MS. Much simpler total ion chromatograms were obtained by ATD-GC/MS than by flash pyrolysis with a Curie-point pyrolyzer, permitting much easier interpretation. Ions at m/z 206, 135, and 107 were fingerprints in the characteristic mass spectra obtained by ATD-GC/MS for TOPF resin in the vulcanized rubber. 1H-Indene, styrene, and isolongifolene were observed as their characteristic mass spectra in the pyrolyzate of the rosin-modified terpene resin. From the cashew resin, phenol, 3-methylphenol, and 4-(1,1,3, 3-tetramethylbutyl)phenol were obtained as the characteristic pyrolyzates by discontinuous thermal extraction via ATD-GC/MS. Copyright 1999 John Wiley & Sons, Ltd. PMID:10589102

  19. Separation and Purification of Two Flavone Glucuronides from Erigeron multiradiatus (Lindl.) Benth with Macroporous Resins

    PubMed Central

    Zhang, Zhi-feng; Liu, Yuan; Luo, Pei; Zhang, Hao

    2009-01-01

    Scutellarein-7-O-?-D-glucuronide (SG) and apigenin-7-O-?-D-glucuronide (AG) are two major bioactive constituents with known pharmacological effects in Erigeron multiradiatus. In this study, a simple method for preparative separation of the two flavone glucuronides was established with macroporous resins. The performance and adsorption characteristics of eight macroporous resins including AB-8, HPD100, HPD450, HPD600, D100, D101, D141, and D160 have been evaluated. The results confirmed that D141 resin offered the best adsorption and desorption capacities and the highest desorption ratio for the two glucuronides among the tested resins. Sorption isotherms were constructed for D141 resin under optimal ethanol conditions and fitted well to the Freundlich and Langmuir models (R2 > 0.95). Dynamic adsorption and desorption tests was performed on column packed with D141 resin. After one-run treatment with D141 resin, the two-constituent content in the final product was increased from 2.14% and 1.34% in the crude extract of Erigeron multiradiatus to 24.63% and 18.42% in the final products with the recoveries of 82.5% and 85.4%, respectively. The preparative separation of SG and AG can be easily and effectively achieved via adsorption and desorption on D141 resin, and the method developed can be referenced for large-scale separation and purification of flavone glucuronides from herbal raw materials. PMID:19918373

  20. Separation and purification of two flavone glucuronides from Erigeron multiradiatus (Lindl.) Benth with macroporous resins.

    PubMed

    Zhang, Zhi-Feng; Liu, Yuan; Luo, Pei; Zhang, Hao

    2009-01-01

    Scutellarein-7-O-beta-D-glucuronide (SG) and apigenin-7-O-beta-D-glucuronide (AG) are two major bioactive constituents with known pharmacological effects in Erigeron multiradiatus. In this study, a simple method for preparative separation of the two flavone glucuronides was established with macroporous resins. The performance and adsorption characteristics of eight macroporous resins including AB-8, HPD100, HPD450, HPD600, D100, D101, D141, and D160 have been evaluated. The results confirmed that D141 resin offered the best adsorption and desorption capacities and the highest desorption ratio for the two glucuronides among the tested resins. Sorption isotherms were constructed for D141 resin under optimal ethanol conditions and fitted well to the Freundlich and Langmuir models (R(2) > 0.95). Dynamic adsorption and desorption tests was performed on column packed with D141 resin. After one-run treatment with D141 resin, the two-constituent content in the final product was increased from 2.14% and 1.34% in the crude extract of Erigeron multiradiatus to 24.63% and 18.42% in the final products with the recoveries of 82.5% and 85.4%, respectively. The preparative separation of SG and AG can be easily and effectively achieved via adsorption and desorption on D141 resin, and the method developed can be referenced for large-scale separation and purification of flavone glucuronides from herbal raw materials. PMID:19918373

  1. Rapid Column Extraction Methods for Urine

    SciTech Connect

    Maxwell, S.L. III

    2000-06-09

    A new fecal analysis method that dissolves plutonium oxide was developed at the Westinghouse Savannah River Site. Diphonix Resin (Eichrom Industries), is used to pre-concentrate the actinides from digested fecal samples. A rapid microwave digestion technique is used to remove the actinides from the Diphonix Resin, which effectively extracts plutonium and americium from acidic solutions containing hydrofluoric acid. After resin digestion, the plutonium and americium are recovered in a small volume of nitric acid that is loaded onto small extraction chromatography columns, TEVA Resin and TRU Resin (Eichrom Industries). The method enables complete dissolution of plutonium oxide and provides high recovery of plutonium and americium with good removal of thorium isotopes such as thorium-228.

  2. Repeated use of ion-exchange resin membranes in calcareous soils

    USGS Publications Warehouse

    Sherrod, S.K.; Belnap, Jayne; Miller, M.E.

    2003-01-01

    This study compared the consistency of nutrient extraction among repeated cycles of ion-exchange resin membrane use. Two sandy calcareous soils and different equilibration temperatures were tested. No single nutrient retained consistent values from cycle to cycle in all treatments, although both soil source and temperature conferred some influence. It was concluded that the most conservative use of resin membranes is single-use.

  3. 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.

  4. Soluble high molecular weight polyimide resins

    NASA Technical Reports Server (NTRS)

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

    1970-01-01

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

  5. Process for Molding Nonreinforced (Neat) Resins

    NASA Technical Reports Server (NTRS)

    Dickerson, G. E.

    1983-01-01

    Void free moldings obtained for neat, condensation, thermosetting resins. Thermally and mechanically treat resin prior to molding to reduce amount of volatiles. With volatiles reduced molding temperature and pressure are applied in way to drive out remaining volatiles during molding.

  6. Method for loading resin beds

    DOEpatents

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

    1978-01-01

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

  7. Selective flotation of fossil resin from Western coal. Final report, July 1, 1990--May 25, 1992

    SciTech Connect

    Jensen, G.F.; Miller, J.D.

    1992-05-25

    The proof-of-concept test program was designed to clarify a number of concerns that have been raised by coal companies who own the valuable resin resource. First, from laboratory bench-scale flotation experiments, a froth product from cleaner flotation containing more than 80% hexane-extractable resin at higher than 80% recovery can be produced. Pilot-plant testing was initiated to demonstrate the selective flotation of fossil resin and to establish a better confidence level in the new technology. Second, pilot-plant testing was designed to evaluate the effect and impact of random variation in slurry solids concentration and feed grade on this new selective fossil resin flotation technology. The flotation performance obtained under these industrial conditions is more realistic for process evaluation. Third, more accurate operating cost data was to be obtained for economic analysis. Fourth, sufficient quantities of the fossil resin concentrate were to be produced from the test program for evaluation by potential industrial users. Fifth, and finally, optimum levels for the operating variables were to be established. Such information was required for eventual scale-up and design of a fossil resin flotation plant. The pilot-plant proof-of-concept testing of selective resinate flotation has demonstrated that: (1) technically, the new flotation technologies discovered at the University of Utah and then improved upon by Advanced Processing Technologies, Inc. provide a highly efficient means to selectively recover fossil resin from coal. The proof-of-concept continuous flotation circuit (about 0.1 tph) resulted in fossil resin recovery with the same separation efficiency as was obtained from laboratory bench-scale testing (more than 80% recovery at about 80% concentrate grade); and (2) economically, the selective flotation process has been shown to be sufficiently profitable to justify the development of a fossil resin industry based on this new flotation process.

  8. Evaluation of TEGDMA leaching from four resin cements by HPLC

    PubMed Central

    Altintas, Subutay Han; Usumez, Aslihan

    2012-01-01

    Objective The aim of this study was to evaluate the elution of TEGDMA from dual cured resin cements, used for bonding of ceramic restoration by high performance liquid chromatography (HPLC). Methods: Forty freshly extracted caries and restoration free molar teeth used in this study. Standardized Class I preparations were prepared in all teeth. Ceramic inlays were cemented with one of the dual cured resin cements (Variolink II, Rely X ARC, Rely X Unicem and Resilute). After cementation, specimens were stored in 75% ethanol solution. HPLC was used to analyze the amounts of TEGDMA in different time intervals. Two-way ANOVA and Tukey HSD tests were used to evaluate the results (P<.05). Results: The amount of TEGDMA eluted from Resilute was the highest and the amount of TEG-DMA eluted from Rely X Unicem was the lowest (P<.05). The total amount of monomers was the highest after 21 days (P<.05). Conclusion: In the case of resin cements, elution of TEGDMA was the highest in Resilute and lowest in Rely X Unicem. The amount of TEGDMA eluted from resin cements was influenced by the time. PMID:22904653

  9. 21 CFR 872.3140 - Resin applicator.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 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 of tooth shade material. (b) Classification. Class I (general controls). The device is exempt from...

  10. 21 CFR 872.3140 - Resin applicator.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 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 of tooth shade material. (b) Classification. Class I (general controls). The device is exempt from...

  11. 21 CFR 872.3140 - Resin applicator.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 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 of tooth shade material. (b) Classification. Class I (general controls). The device is exempt from...

  12. 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 of tooth shade material. (b) Classification. Class I (general controls). The device is exempt from...

  13. 21 CFR 872.3140 - Resin applicator.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 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 of tooth shade material. (b) Classification. Class I (general controls). The device is exempt from...

  14. SRM filament wound case resin characterization studies

    NASA Technical Reports Server (NTRS)

    Chou, L. W.

    1985-01-01

    The amine cured epoxy wet winding resin used in fabrication of the SRM filament wound case is analyzed. High pressure liquid chromatography (HPSC) is utilized extensively to study lot-to-lot variation in both resin and curing agent. The validity of quantitative hplc methodology currently under development in-process resin/catalyst assay is assessed.

  15. 21 CFR 177.1680 - Polyurethane resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyurethane resins. 177.1680 Section 177.1680... Components of Single and Repeated Use Food Contact Surfaces § 177.1680 Polyurethane resins. The polyurethane...) For the purpose of this section, polyurethane resins are those produced when one or more of...

  16. 21 CFR 177.1680 - Polyurethane resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyurethane resins. 177.1680 Section 177.1680... Components of Single and Repeated Use Food Contact Surfaces § 177.1680 Polyurethane resins. The polyurethane...) For the purpose of this section, polyurethane resins are those produced when one or more of...

  17. 21 CFR 177.1680 - Polyurethane resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyurethane resins. 177.1680 Section 177.1680... Components of Single and Repeated Use Food Contact Surfaces § 177.1680 Polyurethane resins. The polyurethane...) For the purpose of this section, polyurethane resins are those produced when one or more of...

  18. 21 CFR 177.1680 - Polyurethane resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyurethane resins. 177.1680 Section 177.1680 Food... of Single and Repeated Use Food Contact Surfaces § 177.1680 Polyurethane resins. The polyurethane...) For the purpose of this section, polyurethane resins are those produced when one or more of...

  19. Method of removing contaminants from plastic resins

    DOEpatents

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

    2008-11-18

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

  20. Method of removing contaminants from plastic resins

    DOEpatents

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

    2007-08-07

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

  1. Method for removing contaminants from plastic resin

    DOEpatents

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

    2008-12-30

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

  2. Investigation of saturated resins in UV coatings

    SciTech Connect

    Costanza, J.R.; Kuzma, E.J.

    1983-01-01

    Results of a study into the use of saturated resins as components of UV cure coatings are presented. Literature support for radical formation and crosslinking of the saturated resins during UV irradiation is discussed. Flexibility, impact resistance, and shrinkage properties of UV coatings are improved by the saturated resins. A simple technique for measuring shrinkage of rigid UV coatings has been developed.

  3. 21 CFR 177.1580 - Polycarbonate resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polycarbonate resins. 177.1580 Section 177.1580... Components of Single and Repeated Use Food Contact Surfaces § 177.1580 Polycarbonate resins. Polycarbonate... with the following prescribed conditions: (a) Polycarbonate resins are polyesters produced by: (1)...

  4. 21 CFR 177.1580 - Polycarbonate resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polycarbonate resins. 177.1580 Section 177.1580... Components of Single and Repeated Use Food Contact Surfaces § 177.1580 Polycarbonate resins. Polycarbonate... with the following prescribed conditions: (a) Polycarbonate resins are polyesters produced by: (1)...

  5. 21 CFR 177.1580 - Polycarbonate resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polycarbonate resins. 177.1580 Section 177.1580... Components of Single and Repeated Use Food Contact Surfaces § 177.1580 Polycarbonate resins. Polycarbonate... with the following prescribed conditions: (a) Polycarbonate resins are polyesters produced by: (1)...

  6. 21 CFR 177.1580 - Polycarbonate resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polycarbonate resins. 177.1580 Section 177.1580... Components of Single and Repeated Use Food Contact Surfaces § 177.1580 Polycarbonate resins. Polycarbonate... with the following prescribed conditions: (a) Polycarbonate resins are polyesters produced by: (1)...

  7. 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.

  8. Polycarbosilazane-Resin Polymerization Process

    NASA Technical Reports Server (NTRS)

    Penn, B.; Ledbetter, F. E., III; Clemons, J.

    1984-01-01

    Process suitable for production of silicon nitride/silicon carbide fibers. High-tensile-strength silicon carbide/silicon nitride fibers prepared by pyrolyzing fibers drawn from melt of polycarbosilazane resin. Such fibers show promise as replacements for carbon fibers in high-strength composites for automotive, aerospace, and other applications where high electrical conductivity of carbon fibers makes them unsuitable.

  9. 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.

  10. Fractionation and utilization of gossypol resin

    SciTech Connect

    Tursunov, A.K.; Dzhailov, A.T.; Fatkhullaev, E.; Sadykov, A.A.

    1985-10-01

    Gossypol resin is formed as a secondary waste product during distillation of fatty acides isolated from cottonseed oil soap stocks; it is insoluble in water but soluble in products of petroleum distillation. For fractionation, gossypol resin was saponified with caustic soda or caustic potash. Using this method, the resin was separated into unsaponifiable (21-24%) and saponifiable (76-79%) parts. Details of the individual fractions of gossypol resin are presented. The unsaponifiable fraction contains hydrocarbons, alcohols, beta-sito-sterol, beta-amyrin, and vitamin E. The fatty acid fraction of the resin is a mixture of fatty acids and lactones.

  11. Analysis of photo-initiators in visible-light-cured dental composite resins.

    PubMed

    Taira, M; Urabe, H; Hirose, T; Wakasa, K; Yamaki, M

    1988-01-01

    Seven commercial visible-light-cured (VL) dental composite resins were analytically studied for identification of the photo-initiator consisting of photo-sensitizer and reducing agent. Gas-liquid chromatography (GC) was used for the determination of the dilute components extracted from the composite resin. Mass spectroscopy (GC-MS) was used for confirmation of the qualitative data obtained by GC. The results showed that all composite resins examined included camphorquinone (CQ) as a photo-sensitizer. The concentration of CQ in the resin phase, however, ranged from 0.17 to 1.03% w/w. The composite resin with hybrid-sized filler tended to have a higher concentration of CQ than did the micro-filled composite resin. As for the reducing agent, two out of seven brands contained dimethylaminoethyl methacrylate (DMAEMA), and one included dimethyl-p-toluidine (DMPTI). The mixing ratio between CQ and the amine in these three composite resins also varied. Another four brands did not contain either DMAEMA or DMPTI, and would utilize different reducing agents. PMID:11039039

  12. Large scale purification of puerarin from Puerariae Lobatae Radix through resins adsorption and acid hydrolysis.

    PubMed

    Guo, Hai-Dong; Zhang, Qing-Feng; Chen, Ji-Guang; Shangguang, Xin-Cheng; Guo, Yu-Xian

    2015-02-01

    Puerarin is the major isoflavone of Puerariae Lobatae Radix. A method for large scale purification of puerarin was developed through resins adsorption and acid hydrolysis. The adsorption properties of six macroporous resins (D101, S-8, H103, X-5, HPD600, AB-8) were compared through the adsorption kinetics and equilibrium adsorption isotherms. Results showed that H103 resin had the best adsorption rate and capacity. The mass transfer zone motion model was further used for analyzing the fixed bed adsorption of H103 resin. Its length of mass transfer zone with 2mg/ml of puerarin in water and 10% ethanol at flow rate of 10ml/min were 41.6 and 47.5cm, while the equilibrium adsorption capacity was 165.03 and 102.88mg/g, respectively. By using 75% ethanol, puerarin could be well desorbed from the resin with recovery of 97.4%. Subsequently, H103 resin was successfully used for puerarin purification from Puerariae Lobatae Radix. The content of total isoflavones and puerarin in the resin adsorption product were 69.25% and 41.78%, respectively, which were about three times increased compared to the crude extract. Then, the product was hydrolyzed by 2.5M HCl at 90°C for 1h. Puerarin with purity of 90% and a byproduct daidzein with purity of 78% were obtained. PMID:25553536

  13. Coupling of Spinosad Fermentation and Separation Process via Two-Step Macroporous Resin Adsorption Method.

    PubMed

    Zhao, Fanglong; Zhang, Chuanbo; Yin, Jing; Shen, Yueqi; Lu, Wenyu

    2015-08-01

    In this paper, a two-step resin adsorption technology was investigated for spinosad production and separation as follows: the first step resin addition into the fermentor at early cultivation period to decrease the timely product concentration in the broth; the second step of resin addition was used after fermentation to adsorb and extract the spinosad. Based on this, a two-step macroporous resin adsorption-membrane separation process for spinosad fermentation, separation, and purification was established. Spinosad concentration in 5-L fermentor increased by 14.45 % after adding 50 g/L macroporous at the beginning of fermentation. The established two-step macroporous resin adsorption-membrane separation process got the 95.43 % purity and 87 % yield for spinosad, which were both higher than that of the conventional crystallization of spinosad from aqueous phase that were 93.23 and 79.15 % separately. The two-step macroporous resin adsorption method has not only carried out the coupling of spinosad fermentation and separation but also increased spinosad productivity. In addition, the two-step macroporous resin adsorption-membrane separation process performs better in spinosad yield and purity. PMID:26077683

  14. 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.

  15. Rapid determination of alpha emitters using Actinide resin.

    PubMed

    Navarro, N; Rodriguez, L; Alvarez, A; Sancho, C

    2004-01-01

    The European Commission has recently published the recommended radiological protection criteria for the clearance of building and building rubble from the dismantling of nuclear installations. Radionuclide specific clearance levels for actinides are very low (between 0.1 and 1 Bq g(-1)). The prevalence of natural radionuclides in rubble materials makes the verification of these levels by direct alpha counting impossible. The capability of Actinide resin (Eichrom Industries, Inc.) for extracting plutonium and americium from rubble samples has been tested in this work. Besides a strong affinity for actinides in the tri, tetra and hexavalent oxidation states, this extraction chromatographic resin presents an easy recovery of absorbed radionuclides. The retention capability was evaluated on rubble samples spiked with certified radionuclide standards (239Pu and 241Am). Samples were leached with nitric acid, passed through a chromatographic column containing the resin and the elution fraction was measured by LSC. Actinide retention varies from 60% to 80%. Based on these results, a rapid method for the verification of clearance levels for actinides in rubble samples is proposed. PMID:15177360

  16. Process for preparing phenolic formaldehyde resole resin products derived from fractionated fast-pyrolysis oils

    SciTech Connect

    Chum, H.L.; Kreibich, R.E.

    1992-02-25

    An improved process is described for preparing phenol-formaldehyde resole resins comprising, replacing a portion of the phenol normally used in making resole resins with a phenol/neutral fractions extract obtained by a process of fractionating fast-pyrolysis oils, wherein the neutral fractions have molecular weights of between about 100 to about 800, and the phenol-containing compositions/neutral fractions extract is soluble in an organic solvent having a solubility parameter of approximately 8.4-9.1 [cal/cm[sup 3

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

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...-Maleic Anhydride Resins *Unsaturated Polyester Resins *Vinyl Toluene Resins *Vinyl Toluene-Acrylate... *Polycarbonates *Polyester Resins *Polyester Resins, Polybutylene Terephthalate *Polyester Resins, Polyoxybenzoate... of this subpart are applicable to the process wastewater discharges resulting from the manufacture...

  18. The root canal bonding of chemical-cured total-etch resin cements.

    PubMed

    Hayashi, Mikako; Okamura, Kenji; Wu, Hongxia; Takahashi, Yutaka; Koytchev, Evgeni V; Imazato, Satoshi; Ebisu, Shigeyuki

    2008-05-01

    Discovering a durable restorative method to reconstruct and reinforce pulpless teeth is a vital key to help prevent root fractures. Complete and firm adhesion of resin cement in root canal dentin using a post is critical to achieve it. The null hypothesis in the present study was that the bond strength of dual-cured and chemical-cured adhesive resin cements to root canal dentin is not affected by their vertical locations in the root canal. In the experiments, extracted human incisors restored with fiber-reinforced posts and adhesive resin cements were subjected to microtensile bond strength testing. Then, the failure modes and the dentin-bonding interfaces were observed. Self-etch and self-adhesive dual-cured resin cements showed frequent pretesting failure despite using a silane coupling agent. Chemical-cured total-etch adhesive material showed stable bonding performances throughout the entire post space and thus has an advantage in post-core restorations. PMID:18436039

  19. The wettability of bonding resins used in the composite resin/glass ionomer 'sandwich technique'.

    PubMed

    Mount, G J

    1989-02-01

    There is some controversy about the significance of the wettability of the unfilled resin bonding agent that is generally recommended for prior application when placing a composite resin restoration. It has been suggested that the degree of viscosity does not matter. However, when investigating the union which is developed between composite resin and glass ionomer cement in the 'sandwich technique', it was noted that when using certain composite resins and their prescribed bonding resins the failure under tensile stress was adhesive at the union rather than cohesive in the cement. Further investigation showed that the bonding resins involved in these failures were more viscous than those bonding resins used in the more successful unions. In this investigation the contact angle of the bonding resin on the surface of glass ionomer cement was used as the measure of viscosity. It is suggested that the degree of viscosity of the bonding resin is significant in the success or otherwise of the 'sandwich technique'. PMID:2650669

  20. Evaluating Resin-Dentin Bond by Microtensile Bond Strength Test: Effects of Various Resin Composites and Placement Techniques

    PubMed Central

    Moosavi, Horieh; Maleknejad, Fatemeh; Forghani, Maryam; Afshari, Elham

    2015-01-01

    Objectives: This in vitro study evaluated the microtensile bond strength (MTBS) of a methacrylate-based compared to a silorane-based resin composite in Class I cavity using different placement techniques. Materials and Methods: Class I cavities with dimension of (4 mm long, 4 mm wide, 3 mm deep) were prepared in extracted sound human molars. The teeth were randomly divided into six groups. The first three groups were filled with Filtek P90 using three methods of insertion; bulk, incremental and snow-plow, and the remaining three groups were filled with Clearfil AP-X using the same three placement techniques. After 24 hours of storage in water at 37°C, the specimens were thermocycled to 1000 cycles. Specimens were prepared for MTBS testing by creating bonded beams obtained from the pulpal floor. Statistical analysis used: Statistical analyses of data were performed by two-way ANOVA/Tukey (α=.05). Results: The experiment showed significant differences between the two resin composites with regard to filling techniques (P<0.05). The MTBS was significantly higher in each of Filtek P90 subgroup compared to Clearfil AP-X ones (P<0.05). With respect to filling technique in both resin composites, bulk insertion showed the significantly lowest MTBS (P<0.05), while no significant difference was found between the outcome of incremental and snow-plow techniques (P>0.05). Conclusion: Silorane-based resin composite as opposed to methacrylate based resin composite and layering placements in contrast to bulk filling method had higher microtensile bond strength. PMID:26966466

  1. 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.

  2. Evaluation of extractables in processed and unprocessed polymer materials used for pharmaceutical applications.

    PubMed

    Stults, Cheryl L M; Ansell, Jennifer M; Shaw, Arthur J; Nagao, Lee M

    2015-02-01

    Polymeric materials are often used in pharmaceutical packaging, delivery systems, and manufacturing components. There is continued concern that chemical entities from polymeric components may leach into various dosage forms, particularly those that are comprised of liquids such as parenterals, injectables, ophthalmics, and inhalation products. In some cases, polymeric components are subjected to routine extractables testing as a control measure. To reduce the risk of discovering leachables during stability studies late in the development process, or components that may fail extractables release criteria, it is proposed that extractables testing on polymer resins may be useful as a screening tool. Two studies have been performed to evaluate whether the extractables profile generated from a polymer resin is representative of the extractables profile of components made from that same resin. The ELSIE Consortium pilot program examined polyvinyl chloride and polyethylene, and another study evaluated polypropylene and a copolymer of polycarbonate and acrylonitrile butadiene styrene. The test materials were comprised of polymer resin and processed resin or molded components. Volatile, semi-volatile, and nonvolatile chemical profiles were evaluated after headspace sampling and extraction with solvents of varying polarity and pH. The findings from these studies indicate that there may or may not be differences between extractables profiles obtained from resins and processed forms of the resin depending on the type of material, the compounds of interest, and extraction conditions used. Extractables testing of polymer resins is useful for material screening and in certain situations may replace routine component testing. PMID:25227309

  3. History of resins in dentistry.

    PubMed

    Peyton, F A

    1975-04-01

    The period of 175 years from 1800 to 1975 represents one of significant advancement in prosthetic and restorative dental service. The transition from the time of ill-fitting dentures, fashioned from naturally occurring materials, to the application of synthetic resins for a long list of dental and surgical purposes described in this symposium represents a typical example of technical and professional advancement that has taken place throughout the world society during this same period. As noted in the beginning of this report, the advancement in dentistry has been possible through the cooperative efforts of contemporary scientists in many related fields. If denistry retains this good working relationship, as it is expected to do, then the advancements within the next two generations can significantly change and improve the practice of dentistry from what is presently known, by the application of additional new and modified dental resins. PMID:1090459

  4. 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.

  5. Advanced thermoplastic resins, phase 2

    NASA Technical Reports Server (NTRS)

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

    1991-01-01

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

  6. High-Temperature Polyimide Resin

    NASA Technical Reports Server (NTRS)

    Vanucci, Raymond D.; Malarik, Diane C.

    1990-01-01

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

  7. Phosphorus-containing imide resins

    NASA Technical Reports Server (NTRS)

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

    1984-01-01

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

  8. Pharmaceutical Applications of Ion-Exchange Resins

    NASA Astrophysics Data System (ADS)

    Elder, David P.

    2005-04-01

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

  9. Optimization of luteolin separation from pigeonpea [Cajanus cajan (L.) Millsp.] leaves by macroporous resins.

    PubMed

    Fu, Yujie; Zu, Yuangang; Liu, Wei; Efferth, Thomas; Zhang, Naijing; Liu, Xiaona; Kong, Yu

    2006-12-29

    In the present study, the performance and separation characteristics of eight macroporous resins for the separation of luteolin (LU) from pigeonpea leaves extracts have been evaluated. The adsorption and desorption properties of LU on macroporous resins including AB-8, NKA-9, NKA-2, D3520, D101, H1020, H103 and AL-2 have been compared. AL-2 resin offers the best adsorption and desorption capacity for LU than other resins based on the research results, and its adsorption data at 25 degrees C fit best to the Freundlich isotherm. Dynamic adsorption and desorption experiments have been carried out with the column packed by AL-2 resin to optimize the separation process of LU from pigeonpea leaves extracts. The optimum parameters for adsorption were sample solution LU concentration 65.5 microg/ml, pH 5, processing volume 3 BV, flow rate 1.5BV/h, temperature 25 degrees C; for desorption were elution solvent ethanol-water (50:50, v/v) 2 BV and followed by ethanol-water (60:40, v/v) 2 BV, and flow rate 1BV/h. After treated with AL-2 resin, the LU content in the product was increased 19.8-fold from 0.129% to 2.55%, with a recovery yield of 78.54%. The results showed that AL-2 resin revealed a good ability to separate LU. Therefore, we conclude that results in this study may provide scientific references for the large-scale LU production from pigeonpea or other plants extracts. PMID:17126843

  10. 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.

  11. ELUTION OF URANIUM FROM RESIN

    DOEpatents

    McLEan, D.C.

    1959-03-10

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

  12. [Purification technology of manninotirose in Rehmanniae Radix Praeparata by D-101 microporous adsorption resin].

    PubMed

    Wang, Xing-xing; Qian, Jun; Wu, Yun; Yan, Bing-peng; Wang, Zhen-zhong; Xiao, Wei

    2015-06-01

    This paper was aim to optimize the purification technology of Rehmanniae Radix Praeparata extract with macroporous adsorption resin. With the content of manninotriose as index, the absorptive flow and time were investigated, as well as kinds, amount, flow of eluent. D-101 type macroporous adsorption resin was the best choice for the purification of manninotriose. The optimized parameters were as follows: the content of manninotriose at 161.16-53.72 mg x g(-1), absorption time 240 min, eluting solvent of purified water, volume flow at 1.5 BV x h(-1), and eluant volume at 6 BV. D-101 type macroporous adsorption resin could significantly increase the purity of Rehmanniae Radix Praeparata extract with the advantage of high absorption, remove most part of impurity, and the effect of semi-works production was better. PMID:26591521

  13. Sulfur geochemistry of hydrothermal waters in Yellowstone National Park, Wyoming, USA. III. An anion-exchange resin technique for sampling and preservation of sulfoxyanions in natural waters

    PubMed Central

    Druschel, Greg K; Schoonen, Martin AA; Nordstrom, D Kirk; Ball, James W; Xu, Yong; Cohn, Corey A

    2003-01-01

    A sampling protocol for the retention, extraction, and analysis of sulfoxyanions in hydrothermal waters has been developed in the laboratory and tested at Yellowstone National Park and Green Lake, NY. Initial laboratory testing of the anion-exchange resin Bio-Rad™ AG1-X8 indicated that the resin was well suited for the sampling, preservation, and extraction of sulfate and thiosulfate. Synthetic solutions containing sulfate and thiosulfate were passed through AG1-X8 resin columns and eluted with 1 and 3 M KCl, respectively. Recovery ranged from 89 to 100%. Comparison of results for water samples collected from five pools in Yellowstone National Park between on-site 1C analysis (U.S. Geological Survey mobile lab) and IC analysis of resin-stored sample at SUNY-Stony Brook indicates 96 to 100% agreement for three pools (Cinder, Cistern, and an unnamed pool near Cistern) and 76 and 63% agreement for two pools (Sulfur Dust and Frying Pan). Attempts to extract polythionates from the AG1-X8 resin were made using HCl solutions, but were unsuccessful. Bio-Rad™ AG2-X8, an anion-exchange resin with weaker binding sites than the AG1-X8 resin, is better suited for polythionate extraction. Sulfate and thiosulfate extraction with this resin has been accomplished with KCl solutions of 0.1 and 0.5 M, respectively. Trithionate and tetrathionate can be extracted with 4 M KCl. Higher polythionates can be extracted with 9 M hydrochloric acid. Polythionate concentrations can then be determined directly using ion chromatographic methods, and laboratory results indicate recovery of up to 90% for synthetic polythionate solutions using AG2-X8 resin columns.

  14. 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.

  15. 21 CFR 177.2510 - Polyvinylidene fluoride resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

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

  16. 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.

  17. Resin selection criteria for tough composite structures

    NASA Technical Reports Server (NTRS)

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

    1983-01-01

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

  18. 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.

  19. Refining of fossil resin flotation concentrate from Western coal. Fourth quarterly final report, October 1, 1993--December 31, 1993

    SciTech Connect

    Jensen, G.F.; Miller, J.D.

    1994-01-05

    Four resinite types, namely yellow, amber, light-brown, and dark-brown in color, occurring in the Wasatch Plateau coal field, are mainly composed of aliphatic components. In contrast coal consists primarily of aromatic ring structures, various oxygen functional groups ({minus}OH, >C=O, {minus}C{minus}O) and few aliphatic chains. The color difference observed among the four hand-sorted resin types is explained by the presence of chromophores (O, S, and N atoms and C=C double bonds) and also by the presence of finely dispersed coal particle inclusions in the resin matrix. The extraction rate for these resin types follows the order yellow > amber > light-brown > dark-brown. Hexane purified resin from all resin types closely resembles the properties of the physically separated yellow resin. Resinites are distinct from other coal macerals, which show a high heat value and high volatile matter content. The four resin types also show distinct differences among certain physical and chemical properties such as density, and softening point. All these properties were noted to change gradually from yellow to dark-brown resin.

  20. RAPID MEASUREMENTS OF NEPTUNIUM OXIDATION STATES USING CHROMATOGRAPHIC RESINS

    SciTech Connect

    Diprete, D; C Diprete, C; Mira Malek, M; Eddie Kyser, E

    2009-03-24

    The Savannah River Site's (SRS) H-Canyon facility uses ceric ammonium nitrate (CAN) to separate impure neptunium (Np) from a high sulfate feed stream. The material is processed using a two-pass solvent extraction purification which relies on CAN to oxidize neptunium to Np(VI) during the first pass prior to extraction. Spectrophotometric oxidation-state analyses normally used to validate successful oxidation to Np(VI) prior to extraction were compromised by this feed stream matrix. Therefore, a rapid chromatographic method to validate successful Np oxidation was developed using Eichrom Industries TRU and TEVA{reg_sign} resins. The method was validated and subsequently transferred to existing operations in the process analytical laboratories.

  1. 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.

  2. 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.

  3. Adsorption characteristics and preparative separation of chaetominine from Aspergillus fumigatus mycelia by macroporous resin.

    PubMed

    Liu, Changqing; Jiao, Ruihua; Yao, Lingyun; Zhang, Yupeng; Lu, Yanhua; Tan, Renxiang

    2016-03-15

    Chaetominine (CHA) is a quinazolinone alkaloid with strong anti-cancer activity produced by Aspergillus fumigatus CY018. For recovering CHA from A. fumigates efficiently, adsorption and desorption capacities of eight macroporous resins were tested in this work. Based on batch experiments, XAD-16 resin was revealed the best adsorption and desorption performance among all the tested resins. Then, adsorption kinetics and adsorption isotherms were constructed on XAD-16 resin, and the experimental data were fitted well to the pseudo first-order kinetics and Freundlick isotherm model. In the dynamic adsorption and desorption, the purity of CHA increased from 0.0314% (w/w) in the crude extract to 57.86% in the final product with recovery yield of 70.56% by a one-step treatment. Moreover, the experiments were also performed in a lab scale-up scale, in which the purity and recovery of CHA were 56.12% (w/w) and 68.02%, respectively. In addition, XAD-16 resin could be recycled 3 times for CHA separation after regeneration without adverse effects on adsorption/desorption performance. These results suggested that XAD-16 resin adsorption could act as a useful and economic method for recovering CHA from A. fumigatus. PMID:26919448

  4. DNA Changes in Tissues Entrapped in Plant Resins (the Precursors of Amber)

    NASA Astrophysics Data System (ADS)

    Rogers, S. O.; Langenegger, K.; Holdenrieder, O.

    There have been many reports characterizing DNA from amber, which is a fossil version of plant resin. Here we report an investigation of the effects of plant resin (from Pseudotsuga menziesii) and drying conditions on the preservation of DNA in biological tissues. We examined the degree of degradation of the DNA by agarose gel electrophoresis of extracted DNA, by polymerase chain reaction, and by DNA sequencing. The plant resin alone appeared to cause little or no damage to DNA. Tissue immersed in plant resin that dried rapidly (exposed to sunlight) contained DNA with little apparent damage. Tissue immersed in the resin that was dried slowly (in shade without sunlight) contained DNA with some degradation (3.5% nucleotide changes). The tissue that was immersed in the resin that was constantly hydrated (by immersion in water) yielded DNA that was severely damaged (50-62% nucleotide changes). Transversions outnumbered transitions in these samples by a ratio of 1.4 : 1. A piece of Baltic amber immersed in water for 5days appeared to be impervious to the water. Thus amber inclusions that initially dried rapidly have the potential to yield undamaged DNA. Those that dried slowly may contain damaged DNA and may be unsuitable for phylogenetic and other studies.

  5. Evaluation of cuspal deflection in premolar teeth restored with low shrinkable resin composite (in vitro study)

    PubMed Central

    Labib, Labib Mohamed; Nabih, Sameh Mahmoud; Baroudi, Kusai

    2015-01-01

    Objectives: This study evaluated cuspal deflection in premolar teeth restored with low shrinkable resin composite. Materials and Methods: A total of 40 human premolars were used for cuspal deflection evaluation in this study. Each group was divided into four equal groups according to the type of resin composite and the adhesive used as follows: group A: Using low shrinkable resin composite (silorane) with its adhesive system; group B: Using low shrinkable composite (silorane) with G-bond; group C: Using Filtek Z350 composite with G-bond; and group D: Using Filtek Z350 composite with AdheSE. Cusp deflection was detected using Universal measuring microscope and laser horizontal metroscope. Results: This study was done to investigate the effect of polymerization shrinkage stresses of two resin composite materials (Filtek Z350 and Filtek P90) on cuspal deflection of mesio-occluso-distal restoration. For this study, the extracted non-carious maxillary second premolars were selected. Forty teeth that showed no more than 5% variation in their dimensions were used. A significant increase in cuspal deflection of cavities restored with the methacrylate-based (Filtek Z350) compared with the silorane (P90) resin-based composites was obtained. Conclusion: The change in the organic matrix or materials formulation of the resin composite using silorane has a positive effect on controlling the cusp deflection. PMID:26759800

  6. 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.

  7. In vitro wear of flowable resin composite for posterior restorations.

    PubMed

    Shinkai, Koichi; Taira, Yoshihisa; Suzuki, Shiro; Suzuki, Masaya

    2016-01-01

    The purpose of this study was to examine three- and two-body wear values of flowable resin composites for posterior restorations, using a mechanical loading device. The cavities prepared on flattened extracted molars were restored with flowable resin composites (Clearfil Majesty LV: MLV, Estelite Flow Quick: EFQ, Beautifil Flow Plus F00: BFP, and MI Fill: MIF) using accompanying adhesive systems. A universal resin composite (Clearfil Majesty) was used as a control. The specimens were subjected to in vitro three- and two-body wear testing. MLV showed high wear value (three-body: 14.69 µm, two-body: 0.268 mm(3)) compared with other materials tested in both three- and two-body wear tests. BFP showed high three-body wear value (5.78 µm), whereas low two-body wear value (0.008 mm(3)). MIF and EFQ showed equivalent wear values (MIF, three-body: 0.42 µm, two-body: 0.026 mm(3); EFQ, three-body: 1.15 µm, two-body: 0.14 mm(3)) to that of the control in both wear tests. PMID:26843441

  8. Microleakage in class V gingiva-shaded composite resin restorations

    PubMed Central

    Poggio, Claudio; Chiesa, Marco; Dagna, Alberto; Colombo, Marco; Scribante, Andrea

    2012-01-01

    Summary The purpose of this study was to evaluate the microleakage in Class V cavities restored with a new gingiva-shaded microhybrid composite resin and with a conventional microhybrid composite resin using three different dentin bonding systems (DBS). Class V cavities were prepared in sixty freshly extracted human teeth with the incisal margin in enamel and the apical margin in dentin/cementum. Restored specimens, after thermocycling, were placed in 2% methylene blue solution for 24 hours. Longitudinal sections were obtained and studied with a stereomicroscope for assessment of the microleakage according to degree of dye penetration (scale 0–3). Data were analyzed with Kruskal-Wallis test and with Mann-Whitney U-test. In this study there was no leakage in enamel: all the cavities showed no dye penetration at the incisal margins (located in enamel). None of the DBS used eliminated microleakage in apical margins (located in dentin or cementum): three-step total-etch and single-step self-etch were more effective in reducing microleakage in dentin margins when compared with two-step total-etch. This in vitro study concluded that microleakage in Class V cavities restored with the composite resins tested is similar. PMID:22783451

  9. Calysolins I-IV, resin glycosides from Calystegia soldanella.

    PubMed

    Takigawa, Ayako; Muto, Haruka; Kabata, Kiyotaka; Okawa, Masafumi; Kinjo, Junei; Yoshimitsu, Hitoshi; Nohara, Toshihiro; Ono, Masateru

    2011-11-28

    Four new resin glycosides having intramolecular cyclic ester structures (jalapins), named calysolins I-IV (1-4), were isolated from the methanol extract of leaves, stems, and roots of Calystegia soldanella , along with one known jalapin (5) derivative. The structures of 1-4 were determined on the basis of spectroscopic data and chemical evidence. They fall into two types, one having a 22-membered ring (1 and 4) and the other with a 27-membered ring (2 and 3). The sugar moieties of 1-4 were partially acylated by some organic acids. Compound 4 is the first example of a hexaglycoside of jalapin. PMID:21992192

  10. 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.

  11. Phosphorus-containing imide resins

    NASA Technical Reports Server (NTRS)

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

    1985-01-01

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

  12. Getting tough with epoxy resins

    SciTech Connect

    Bertram, J.L.; Puckett, P.M. )

    1994-03-01

    A growth market for polymer-matrix composites (PMCs) is the replacement of metals in aerospace applications to reduced weight and consolidate parts. However, to substitute for metal primary structures, composites must combine improved strength and toughness with moisture resistance and the ability to withstand high temperatures. Even though higher performance composites are in demand, huge cuts in defense spending have caused a dramatic slowdown in R and D on new polymers. Instead, composites manufacturers are seeking ways to extend the limits of existing materials, such as epoxy, the workhorse'' PMC matrix resin. Suppliers have responded by expanding conventional epoxy technology.

  13. Analysis and aging of unsaturated polyester resins in contemporary art installations by NMR spectroscopy.

    PubMed

    Stamatakis, Georgios; Knuutinen, Ulla; Laitinen, Kai; Spyros, Apostolos

    2010-12-01

    Two original art installations constructed from unsaturated polyester resins (UPR) and four different reference UPR products (before and after UVB aging) were analyzed by high-resolution 1D and 2D nuclear magnetic resonance (NMR) spectroscopy. Breaking strain studies were also conducted for the four UPR model products before and after different aging procedures (moisture, UVB exposure, melt/freeze). NMR analysis of the chemical composition of the UPR resin extracts showed they contain several low MW organic compounds and oligomers rich in polar -OH groups that play a significant role in the degradation behavior of the composite UPR materials. Statistical analysis of the NMR compositional data showed that styrene and benzaldehyde contents can be used to differentiate between fresh and aged UPR samples. The phthalate and propylene glycol unit speciation (esterified, primary or secondary -OH) of the extracts provided evidence that UPR resin C was used in the construction of the two art installations, and direct comparison of (1)H and (13)C NMR spectra verified this compositional similarity. UPR resin C was shown by both NMR and breaking strain studies to be the reference UPR most susceptible to degradation by different aging procedures, a characteristic attributed to the lower styrene content of resin C. PMID:20922516

  14. TMI-2 purification demineralizer resin study

    SciTech Connect

    Thompson, J D; Osterhoudt, T R

    1984-05-01

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

  15. 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.

  16. Polyisoprenylated benzophenones from Clusia floral resins.

    PubMed

    Porto, A L; Machado, S M; de Oliveira, C M; Bittrich, V; Amaral, M C; Marsaioli, A J

    2000-12-01

    From the floral resins of various Clusia species, seven polyisoprenylated benzophenones were isolated. HPLC allowed their quantification in all resins, revealing a distribution of benzophenone derivatives distinct from each other. In some species the staminal oils were collected and oleic, stearic and palmitic acids were the main constituents. PMID:11190392

  17. Fluorinated diamond bonded in fluorocarbon resin

    DOEpatents

    Taylor, Gene W.

    1982-01-01

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

  18. [Delayed asthma bronchiale due to epoxy resin].

    PubMed

    Authried, Georg; Al-Asadi, Haifaa; Møller, Ulla; Sherson, David Lee

    2013-10-28

    Epoxy resin is a low molecular weight agent, which can cause both acute and delayed allergic reactions. However, it is known causing skin reactions with direct or airborne contact. Rarely it can cause airway reactions like asthma bronchiale. We describe a case of a windmill worker who developed delayed asthma bronchiale due to airborne contact with epoxy resin. PMID:24629199

  19. 21 CFR 177.1500 - Nylon resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Nylon resins. 177.1500 Section 177.1500 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1500 Nylon resins. The nylon...

  20. 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... resins for use in contact with all types of food except alcoholic beverages containing more than...

  1. 21 CFR 177.1655 - Polysulfone resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...) of this section. N-methyl-2-pyrrolidone Not to exceed 0.01 percent (100 parts per million) as...-phenyleneisopropylidene-p-phenylene) resins (CAS Reg. No. 25154-01-2) consisting of basic resins produced when the... by osmotic pressure in monochlorobenzene; or (2) 1,1′-Sulfonylbis polymer with...

  2. 21 CFR 177.1655 - Polysulfone resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... (CAS Reg. No. 25154-01-2) consisting of basic resins produced when the disodium salt of 4,4...; or (2) 1,1′-Sulfonylbis polymer with 4,4′-(1-methylethylidene)bis (minimum 92 percent) and 4,4... as residual solvent in finished basic resin in paragraph (a)(1) of this section....

  3. 21 CFR 177.1655 - Polysulfone resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...) of this section. N-methyl-2-pyrrolidone Not to exceed 0.01 percent (100 parts per million) as...-phenyleneisopropylidene-p-phenylene) resins (CAS Reg. No. 25154-01-2) consisting of basic resins produced when the... by osmotic pressure in monochlorobenzene; or (2) 1,1′-Sulfonylbis polymer with...

  4. 21 CFR 177.1655 - Polysulfone resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...) of this section. N-methyl-2-pyrrolidone Not to exceed 0.01 percent (100 parts per million) as...-phenyleneisopropylidene-p-phenylene) resins (CAS Reg. No. 25154-01-2) consisting of basic resins produced when the... by osmotic pressure in monochlorobenzene; or (2) 1,1′-Sulfonylbis polymer with...

  5. 21 CFR 177.1655 - Polysulfone resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...) of this section. N-methyl-2-pyrrolidone Not to exceed 0.01 percent (100 parts per million) as...-phenyleneisopropylidene-p-phenylene) resins (CAS Reg. No. 25154-01-2) consisting of basic resins produced when the... by osmotic pressure in monochlorobenzene; or (2) 1,1′-Sulfonylbis polymer with...

  6. 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.

  7. Terpenoid Oligomers of Dammar Resin.

    PubMed

    Bonaduce, Ilaria; Di Girolamo, Francesca; Corsi, Iacopo; Degano, Ilaria; Tinè, Maria Rosaria; Colombini, Maria Perla

    2016-04-22

    Dammar is a triterpenoid resin containing a volatile fraction, a monomeric fraction, and a high-molecular weight fraction. Although the low-molecular-weight components comprising sesquiterpenoids and triterpenoids have been extensively studied, the nature of the macromolecular components is still not fully understood, and different and sometimes contradictory theories have been proposed. The aim of this paper is to clarify the nature of the macromolecular components of dammar resin. A multianalytical approach was adopted based on thermoanalytical-thermogravimetric analysis (TGA), and thermogravimetric analysis coupled with Fourier transform infrared spectroscopy (TGA/FTIR)-and mass spectrometric techniques-direct exposure mass spectrometry (DE/MS), pyrolysis coupled to gas chromatography and mass spectrometry (Py/GC/MS), flow injection analysis electrospray ionization mass spectrometry (FIA/ESI/MS), and gas chromatography/mass spectrometry (GC/MS). The data indicate that the oligomeric fraction comprises triterpenoids bound through ester bonds, and that these triterpenoids are the same as those found in the free terpenoid fraction. The oligomeric fraction also includes triterpenoids containing carbonyl moieties, such as formyl groups, thus suggesting that these are involved in the esters in their corresponding enolic form. PMID:26981624

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

    NASA Astrophysics Data System (ADS)

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

    2013-12-01

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

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

    PubMed

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

    2004-06-01

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

  10. Posterior adhesive composite resin: a historic review.

    PubMed

    Fusayama, T

    1990-11-01

    Since development of the BIS-GMA composite resin, there have been many innovations to improve the physical properties for posterior use. Subsequent development of a caries detector and chemically adhesive composite resin has further revolutionally raised the value of composite resin restoration, replacing the traditional restorative system of mechanical approach by the new system of biological approach. In this system only the infected irreversibly deteriorated insensitive tissue, stainable with the caries detector, is removed painlessly. The cavity is immediately filled with the composite resin with no further tissue reduction for retention or resistance form or extension for prevention. Both enamel and dentin walls are etched by a single etchant without lining. The chemical adhesion to the cavity margin and wall minimizes the marginal failure in size and prevalence and prevents secondary caries penetration along the wall. The chemically adhesive composite resin is thus a useful restorative material much kinder to teeth than amalgam. PMID:2090811

  11. Release and toxicity of dental resin composite.

    PubMed

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

    2012-09-01

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

  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. Crypthophilic acids A, B, and C: resin glycosides from aerial parts of Scrophularia crypthophila.

    PubMed

    Cali?, Ihsan; Sezgin, Ykselen; Dnmez, Ali A; Redi, Peter; Tasdemir, Deniz

    2007-01-01

    The water-soluble part of the methanolic extract from the aerial parts of Scrophularia crypthophila, through chromatographic methods, yielded three new resin glycosides, crypthophilic acids A - C (1-3). Compounds 1-3 are tetraglycosides of (+)-3S,12S-dihydroxypalmitic acid. The structures of these and 10 known compounds were elucidated by spectroscopic and chemical means. All natural resin glycosides known so far have been obtained from Convolvulaceae plants; this is the first report of such glycosides from another, taxonomically unrelated family (Scrophulariaceae). PMID:17253848

  15. High-yield resin fractionation using a liquid/liquid centrifuge

    NASA Astrophysics Data System (ADS)

    Wanat, Stan F.; Rahman, M. D.; Narasimhan, Balaji; McKenzie, Douglas S.; Cook, Michelle M.

    2000-06-01

    Resins used in photoresist manufacturing are often relatively expensive once processing steps (fractionation e.g.) and yield losses are factored into the net cost. We have previously reported on the merits of using an economically more attractive fractionation process using a liquid/liquid centrifuge. Further refinements of this method indicate that waste streams could be reduced by recycling the extractant phase and that lower molecular weight fractions removed from the starting resin might be used in making other resist ingredients [speed enhancers, photoactive compound (PAC) backbones e.g.]. Both of these improvements would reduce the overall manufacturing costs of making resist raw materials and the final products made with them.

  16. The application of macroporous resins in the separation of licorice flavonoids and glycyrrhizic acid.

    PubMed

    Fu, Boqiang; Liu, Jie; Li, Huan; Li, Lei; Lee, Frank S C; Wang, Xiaoru

    2005-09-30

    Glycyrrhizic acid (GA) and licorice flavonoids (LF) are the two classes of bioactive components in licorice with known pharmacological effects. But long-term excessive intake of GA may cause sodium retention and hypertension. In this study, the performance and adsorption characteristics of four widely used macroporous resins for the separation of deglycyrrhizinated, flavonoids enriched licorice has been critically evaluated. The sorption and desorption properties of LF and GA on macroporous resins including XDA-1, LSA-10, D101 and LSA-20 have been compared. The adsorption capacity was found to depend strongly on the pH of the feed solution. XDA-1 offers much higher adsorption capacity for GA and LF than other resins, and its adsorption data fit the best to the Freundlich isotherm. XDA-1 also shows much higher adsorption affinity towards LF than that of GA based on calculated results from the measured adsorption isotherms. Dynamic adsorption and desorption experiments have been carried out on a XDA-1 resin packed column to obtain optimal parameters for separating GA and LF. An enriched LF extract (about 21.9% purity) free of GA, and an enriched GA extract with 66% purity can be separated from crude licorice extract in one run. PMID:16130766

  17. Resin/graphite fiber composites

    NASA Technical Reports Server (NTRS)

    Cavano, P. J.

    1974-01-01

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

  18. Mineralogy of fossil resins in Northern Eurasia

    NASA Astrophysics Data System (ADS)

    Bogdasarov, M. A.

    2007-12-01

    The investigation is focused on identification and origin of fossil resins from the Cretaceous, Tertiary, and Quaternary sediments of Northern Eurasia on the basis of detailed study of their physical and chemical characteristics: morphology; size; mass; density; optical, mechanical, and thermal properties; chemical composition; etc. The composition of amorphous organic minerals with polymeric structure, fossil resins included, is studied with IR spectrometry, the EPR method, derivatography at low heating rates, XRD, chemical analysis, emission spectrometry, etc. The results of investigation summarized for the Baltic-Dnieper, North Siberian, and Far East amber-bearing provinces show some similarity of fossil resins in combination with specific features inherent to each province. Resins from the Baltic-Dnieper province should be termed as amber (succinite). Their variety is the most characteristic of Northern and Eastern Europe. Amber-like fossil resins from the North Siberian and Far East provinces are irrelevant to succinite. They usually occur as brittle resins, namely, retinite and gedanite, without jewelry value. Viscous fossil resin rumänite with an expected high economic value occurs in the Far East, on the shore of Sakhalin Island.

  19. Use of EIChroM TRU RESIN in the determination of Americium, Plutonium and Uranium in air filter and water samples

    SciTech Connect

    Berne, Anna

    1995-03-01

    TRU Resin, an extraction chromatographic material ((octyl (phenyl)-N,Ndiisobutylcarbamoylmethylphosphene oxide (CMPO) dissolved in tributyl phosphate (TBP)) manufactured by EIChroM Industries, was tested for its actinide sorption and desorption characteristics. A study was initiated to demonstrate the effectiveness of extracting plutonium, americium and uranium from water and air filter samples from the Environmental Measurements Laboratory’s Quality Assessment Program (QAP), and the effectiveness of subsequent desorption of one chemical species at a time in order to prepare each of them for spectrometry. Crossover of plutonium into the americium fraction with the TRU Resin was observed and could not be eliminated while using TRU Resin only. However, prior extraction of plutonium using an anion exchange resin can overcome this problem. A method for the determination of americium is proposed which combines the extraction of plutonium onto Bio-Rad AG 1-X8 anion exchange resin with the extraction of americium using the TRU Resin. This method was tested on three triplicate sets of QAP air filters and two triplicate sets of QAP water samples. The recoveries ranged from 70 to 90 percent, and the results were identical to those obtained by the existing methods. The time required to perform the analysis for americium was shortened from 5 weeks to 1 week.

  20. Use of EIChroM`s TRU resin in the determination of americium, plutonium and uranium in air filter and water samples

    SciTech Connect

    Berne, A.

    1995-12-01

    TRU Resin, an extraction chromatographic material (octyl (phenyl)-N,Ndiisobutylcarbamoyl-methylphosphene oxide (CMPO) dissolved in tributyl phosphate (TBP)) manufactured by EIChroM Industries, was tested for its actinide sorption and desorption characteristics. A study was initiated to demonstrate the effectiveness of extracting plutonium, americium and uranium from water and air filter samples from the Environmental Measurements Laboratory`s Quality Assessment Program (QAP), and the effectiveness of subsequent desorption of one chemical species at a time in order to prepare each of them for a spectrometry. Crossover of plutonium into the americium fraction with the TRU Resin was observed and could not be eliminated while using TRU Resin only. However, prior extraction of plutonium using an anion exchange resin can overcome this problem. A method for the determination of americium is proposed which combines the extraction of plutonium onto Bio-Rad AG 1-X8 anion exchange resin with the extraction of americium using the TRU Resin. This method was tested on three triplicate sets of QAP air filters and two triplicate sets of QAP water samples. The recoveries ranged from 70 to 90 percent, and the results were identical to those obtained by the existing methods. The time required to perform the analysis for americium was shortened from 5 weeks to 1 week.

  1. Literature search on the use of resins for treatment of radioactive wastes

    SciTech Connect

    AlMahamid, I.; Smith, B.M.

    1997-10-01

    Over 100 commercial providers with mixed-waste treatability capabilities exist in the US. The maturity level of these technologies varies from a bench scale to a pilot or a commercial scale. The techniques include deactivation, chemical oxidation, recovery of metals, stabilization, vitrification, incineration, biodegradation, and chemical extraction. This report focuses on the use of resins to remove actinides and heavy metals from aqueous waste streams. Only the literature that described resins with high removing efficiency are presented here. The majority of the literature reviewed are proceedings and national or international reports ordered through the Berkeley Lab Library. Some of the reports that the authors requested have not yet arrived. Only a few papers were found in the open literature (journals or magazines). Although this report does not include all existing references, it provides an accurate assessment of efficient resins to be considered for waste minimization procedures. 70 refs.

  2. [Determination of residual organic solvents and macroporous resin residues in Akebia saponin D].

    PubMed

    Wang, Qiao-han; Yang, Xiao-lin; Xiao, Wei; Wang, Zhen-zhong; Ding, Gang; Huang, Wen-zhe; Yang, Zhong-lin

    2015-05-01

    According to ICH, Chinese Pharmacopoeia and supplementary requirements on the separation and purification of herbal extract with macroporous adsorption resin by SFDA, hexane, acetidine, ethanol, benzene, methyl-benzene, o-xylene, m-xylene, p-xylene, styrene, diethyl-benzene and divinyl-benzene of residual organic solvents and macroporous resin residues in Akebia saponin D were determined by headspace capillary GC. Eleven residues in Akebia saponin D were completely separated on DB-wax column, with FID detector, high purity nitrogen as the carry gases. The calibration curves were in good linearity (0.999 2-0.999 7). The reproducibility was good (RSD < 10%). The average recoveries were 80.0% -110%. The detection limit of each component was far lower than the limit concentration. The method is simple, reproducible, and can be used to determine the residual organic solvents and macroporous resin residues in Akebia saponin D. PMID:26390656

  3. Nanoindentation Study of Resin Impregnated Sandstone and Early-Age Cement Paste Specimens

    NASA Astrophysics Data System (ADS)

    Zhu, W.; Fonteyn, M. T. J.; Hughes, J.; Pearce, C.

    Nanoindentation testing requires well prepared samples with a good surface finish. Achieving a good surface finish is difficult for heterogeneous materials, particularly those with weak and fragile structures/phases, which are easily damaged or lost during preparation. The loss of weak structures can be drastically reduced by impregnating the sample with a resin before cutting and polishing. This technique is commonly used in SEM microscopy but has not been used for nanoindentation-testing before. This paper reports an investigation to extract micro-mechanical properties of different phases in resin impregnated sandstone and 1-day hydrated cement samples. The results appeared to show that it is feasible to use resin impregnated specimens for nanoindentation study of both materials.

  4. 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 reduces the cesium distribution coefficient of the resin beads, as does irradiation. Higher temperatures during irradiation or during contact with the simulant solution further reduce the cesium distribution coefficient.

  5. 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).

  6. Class II Resin Composites: Restorative Options.

    PubMed

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

    2015-10-01

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

  7. 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.

  8. Chemical Characterization of Phenol/Formaldehyde Resins

    NASA Technical Reports Server (NTRS)

    Brayden, T. H.

    1986-01-01

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

  9. Properties of a nanodielectric cryogenic resin

    SciTech Connect

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

    2010-01-01

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

  10. Absolute stereostructures of polypodane- and octanordammarane-type triterpenes with nitric oxide production inhibitory activity from guggul-gum resins.

    PubMed

    Matsuda, Hisashi; Morikawa, Toshio; Ando, Shin; Oominami, Hideo; Murakami, Toshiyuki; Kimura, Ikuko; Yoshikawa, Masayuki

    2004-06-01

    The methanolic extract from guggul-gum resin, the resin of Balsamodendron mukul, was found to inhibit nitric oxide production in lipopolysaccharide-activated mouse peritoneal macrophages (IC(50) = 13 microg/mL). From the methanolic extract, three new polypodane-type triterpenes, myrrhanol B and myrrhanones B and A acetate, and a new octanordammarane-type triterpene, epimansumbinol, were isolated together with 17 known compounds including progesterone and the related steroids. The absolute stereostructures of new triterpenes were elucidated on the basis of chemical and physicochemical evidence. The several constituents showed inhibitory effects on nitric oxide production and induction of inducible nitric oxide synthase. PMID:15142562

  11. 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...

  12. Recovery of gallium(III) from strongly alkaline media using a Kelex-100-loaded ion-exchange resin

    SciTech Connect

    Nakayama, Morio; Egawa, Hiroaki

    1997-10-01

    Kelex-100 [7-(4-ethyl-1-methyloctyl)-8-hydroxyquinoline] is an important liquid-chelating ion exchanger in hydrometallurgy and a highly selective extractant for gallium (Ga). In this study, Kelex-100-loaded ion-exchange resins were prepared for the recovery of Ga(III) from sodium aluminate solutions (Bayer solution) used in the Bayer process. When macroporous type ion-exchange resins were used as polymer matrices for loading Kelex-100, the physical pore structure and the ion-exchange group significantly affected the adsorption of Ga(III) from strongly alkaline media on the Kelex-100-loaded resin. In particular, the Kelex-100-loaded carboxylic type resin having a macroporous structure showed a high capacity for Ga(III) in concentrated NaOH solution and effectively recovered Ga(III) from the Bayer solution containing large amounts of aluminum(III).

  13. 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.

  14. The efficiency of different light sources to polymerize resin cement beneath porcelain laminate veneers.

    PubMed

    Usumez, A; Ozturk, A N; Usumez, S; Ozturk, B

    2004-02-01

    Plasma arc light units for curing resin composites have been introduced with the claim of relatively short curing times. The purpose of this study was to evaluate the efficiency of two different light sources to polymerize dual curing resin cement beneath porcelain laminate veneers. Twenty extracted healthy human maxillary centrals were used. Teeth were sectioned 2 mm below the cemento-enamel junction and crown parts were embedded into self-cure acrylic resin, labial surface facing up. Cavity preparation was carried out on labial surfaces. These teeth were divided into two groups of 10 each. The resin cement/veneer combination was exposed to two different photo polymerization units. A conventional halogen light (Hilux 350, Express Dental Products) and a plasma arc light (Power PAC, ADT) were used to polymerize resin cement. Ten specimens were polymerized conventionally (40 s) and the other specimens by plasma arc curing (PAC) (6 s). Two samples from each tooth measuring 1.2 x 1.2 x 5 mm were prepared. These sections were subjected to microshear testing and failure values were recorded. Statistically significant differences were found between the bond strength of veneers exposed to conventional light and PAC unit (P < 0.001). Samples polymerized with halogen light showed better bond strength. The results of this study suggest that the curing efficiency of PAC through ceramic was lower compared with conventional polymerization for the exposure durations tested in this study. PMID:15009601

  15. Molecular composition and paleobotanical origin of Eocene resin from northeast India

    NASA Astrophysics Data System (ADS)

    Rudra, Arka; Dutta, Suryendu; Raju, Srinivasan V.

    2014-06-01

    The molecular composition of fossil resins from early to middle Eocene coal from northeast India, has been analyzed for the first time to infer their paleobotanical source. The soluble component of fossil resin was analyzed using gas chromatography-mass spectrometry (GC-MS). The resin extracts are composed of cadalene-based C15 sesquiterpenoids and diagenetically altered triterpenoids. The macromolecular composition was investigated using pyrolysis gas chromatography-mass spectrometry (Py-GC-MS) and Fourier transform infrared (FTIR) spectroscopy. The major pyrolysis products are C15 bicyclic sesquiterpenoids, alkylated naphthalenes, benzenes and a series of C17-C34 n-alkene- n-alkane pairs. Spectroscopic analysis revealed the dominance of aliphatic components. The presence of cadalene-based sequiterpenoids confirms the resin to be Class II or dammar resin, derived from angiosperms of Dipterocarpaceae family. These sesquiterpenoids are often detected in many SE Asian fluvio-deltaic oils. Dipterocarpaceae are characteristic of warm tropical climate suggesting the prevalence of such climate during early Eocene in northeast India.

  16. Epoxy resin synthesis using low molecular weight lignin separated from various lignocellulosic materials.

    PubMed

    Asada, Chikako; Basnet, Sunita; Otsuka, Masaya; Sasaki, Chizuru; Nakamura, Yoshitoshi

    2015-03-01

    A low molecular weight lignin from various lignocellulosic materials was used for the synthesis of bio-based epoxy resins. The lignin extracted with methanol from steam-exploded samples (steaming time of 5 min at steam pressure of 3.5 MPa) from different biomasses (i.e., cedar, eucalyptus, and bamboo) were functionalized by the reaction with epichlorohydrin, catalyzed by a water-soluble phase transfer catalyst tetramethylammonium chloride, which was further reacted with 30 wt% aqueous NaOH for ring closure using methyl ethyl ketone as a solvent. The glycidylated products of the lignin with good yields were cured to epoxy polymer networks with bio-based curing agents i.e., lignin itself and a commercial curing agent TD2131. Relatively good thermal properties of the bio-based epoxy network was obtained and thermal decomposition temperature at 5% weight loss (Td5) of cedar-derived epoxy resin was higher than that derived from eucalyptus and bamboo. The bio-based resin satisfies the stability requirement of epoxy resin applicable for electric circuit boards. The methanol-insoluble residues were enzymatically hydrolyzed to produce glucose. This study indicated that the biomass-derived methanol-soluble lignin may be a promising candidate to be used as a substitute for petroleum-based epoxy resin derived from bisphenol A, while insoluble residues may be processed to give a bioethanol precursor i.e., glucose. PMID:25572718

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

    PubMed

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

    2015-01-01

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

  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. Self-indicating amine scavenger resins.

    PubMed

    Cho, Jin Ku; White, Peter D; Klute, Wolfgang; Dean, Tony W; Bradley, Mark

    2004-03-01

    Self-indicating methylisocyanate resin, which functions as both a scavenger and an indicator for amines, was used for in-situ reaction monitoring and purification of a urea based library. PMID:14973578

  20. 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.

  1. 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.

  2. 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.

  3. 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.

  4. Method for regenerating magnetic polyamine-epichlorohydrin resin

    DOEpatents

    Kochen, Robert L.; Navratil, James D.

    1997-07-29

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

  5. Cesium-specific phenolic ion exchange resin

    SciTech Connect

    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.

  6. Cesium-specific phenolic ion exchange resin

    DOEpatents

    Bibler, Jane P.; Wallace, Richard M.

    1995-01-01

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

  7. Nano composite from coal modified novolac resin

    SciTech Connect

    Ahmaruzzaman, M.; Sharma, D.K.

    2007-07-01

    Coal-modified novolac/clay nanocomposites were synthesized using clay as reinforcing materials. It was found that coal-modified novolac resin based silica nano-composites showed improved tensile strength compared to that of neat novolac resin. The structure of the nanocomposites was characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Scanning electron microscopy (SEM) studies have also been undertaken to see the morphology of the nanocomposites prepared. The results obtained are being reported.

  8. Chemical derivatization of Resorcinol-Formaldehyde resin leading to enhanced chemical/oxidative stability of the resin

    SciTech Connect

    Hubler, T.L.; Franz, J.A.

    1996-10-01

    Resorcinol-Formaldehyde (R-F) resin is a candidate regenerable ion-exchange resin for removal of radioactive cesium from highly alkaline waste tank supernates at both the Hanford and Savannah River sites. Our previous investigations into the structure/function relationships of R-F resin have shown that the R-F resin undergoes facile oxidation to produce, para-bisquinones, with loss of ion-exchange sites, hence lowered performance of the resin for cesium ion-exchange. Our studies have also shown that Phenol-Formaldehyde (P-F) resin has a substantially lower capacity compared to R-F resin, based on predicted values, because over half the ion-exchange sites of the P-F resin undergo etherification during the standard synthetic procedures used for preparation of these resins. In this report, we present our studies into rational synthetic solutions to enhance the chemical/oxidative stability of R-F resin.

  9. Cleanup of TMI-2 demineralizer resins

    SciTech Connect

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

    1985-01-01

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

  10. Ion Exchange Temperature Testing with SRF Resin

    SciTech Connect

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

    2012-03-01

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

  11. 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.

  12. Separation and purification of amygdalin from thinned bayberry kernels by macroporous adsorption resins.

    PubMed

    Wang, Tao; Lu, Shengmin; Xia, Qile; Fang, Zhongxiang; Johnson, Stuart

    2015-01-15

    To utilize the low-value thinned bayberry (Myrica rubra Sieb. et Zucc) kernels (TBKs) waste, an efficient method using macroporous adsorption resins (MARs) for separation and purification of amygdalin from TBKs crude extracts was developed. An aqueous crude sample was prepared from a methanol TBK extract, followed by resin separation. A series of MARs were initially screened for adsorption/desorption of amygdalin in the extract, and D101 was selected for characterization and method development. The static adsorption data of amygdalin on D101 was best fitted to the pseudo-second-order kinetics model. The solute affinity toward D101 at 30 °C was described and the equilibrium experimental data were well-fitted to Langmuir and Freundlich isotherms. Through one cycle of dynamic adsorption/desorption, the purity of amygdalin in the extract, determined by HPLC, increased about 17-fold from 4.8% to 82.0%, with 77.9% recovery. The results suggested that D101 resin effectively separate amygdalin from TBKs. PMID:25438243

  13. Effect of resin cement, aging process and root level on the bond strength of the resin-fiber posts

    NASA Astrophysics Data System (ADS)

    Almuhim, Khalid Salman

    Background. Little is known about the long-term clinical bonding effectiveness of the Fiber-reinforced composite (FRC) posts cemented with self-etch adhesive systems. Bond stability and longevity of the cemented post are adversely affected by physical and chemical factors over time, such as expansion and contraction stresses caused by thermal changes and occlusal load. This clinical condition can be simulated in vitro by thermocyclic loading; and bonding effectiveness can be evaluated by applying the micropush out test. Therefore, more in vitro studies are needed to evaluate the bond strength of the fiber posts cemented with different resin cement systems after simulating the artificial aging induced by thermocycling. The aim of this study was to compare the microtensile bond strength of two different resin cement systems (total etch, and self-etch resin cement system) used for cementation of fiber reinforced composite posts in three different aging periods using thermocycling. Methods. Following IRB approval, sixty freshly extracted bicuspid single rooted natural teeth were endodontically treated, and the post-spaces were prepared to receive a fiber-post cemented with either a total etch resin cement (Rely-X Ultimate) or with a self-etch resin cement (Rely-X Unicem). No thermocycling, 20,000 and 40,000 cycles was used to age the specimens. Teeth were randomly allocated into six different groups: G1 - Control: Rely-X Ultimate cement with no thermocycling. G2: Rely-X Ultimate cement with 20,000 thermocycling. G3: Rely-X Ultimate cement with 40,000 thermocycling. G4: Rely-X Unicem cement. G5: Rely-X Unicem cement. G6: Rely-X Unicem cement. Microtensile bond strength determined using a micropush out test on a universal testing machine (MTS). Additionally, the failure mode of each specimen was observed under a stereomicroscope (Olympus) at 40x magnification. Finally, one representative sample was randomly selected from each of the five failure modes for scanning electron microscope (SEM) examination of the surface morphology in order to obtain SEM images of the failure patterns at 29--70x magnifications. Statistical analysis: Nested general linear and generalized linear model was created to look for statistical significance. Level of significance was set at P < 0.05. Results. No significant differences were found on the bond strength between the two types of resin cement systems (total etch and self-etch). Regarding the thermocycling effect, the bond strengths of the group of 40,000 cycles was significantly lower than the 20,000 cycle group. In addition, the bond strengths of the specimens collected from the coronal third of the root were significantly lower than the specimens from the apical third. A Fisher's Exact test was applied to evaluate the failure mode differences, and showed statistically significant differences between the groups. Conclusions . The bond strength to the root canal dentin did not vary with the type of resin cement systems (total-etch vs self-etch). The microtensile bond strength values of FRC posts were significantly affected by increasing the thermocycling, and were significantly different among the different longitudinal levels of the root canal.

  14. 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.

  15. 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.

  16. The influences of N-acetyl cysteine (NAC) on the cytotoxicity and mechanical properties of Poly-methylmethacrylate (PMMA)-based dental resin

    PubMed Central

    Jiao, Yang; Ma, Sai; Li, Jing; Shan, Lequn; Yang, Yanwei; Li, Meng

    2015-01-01

    Objectives. This study aimed to investigate the influences of N-acetyl cysteine (NAC) on cytotoxicity and mechanical properties of Poly-methylmethacrylate (PMMA) dental resins. Methods. Experimental PMMA resin was prepared by incorporating various concentrations of NAC (0, 0.15, 0.3, 0.6 and 0.9 wt.%). MTT assay was performed to investigate viability of human dental pulp cells after exposure to extract of PMMA resin with or without NAC. Cell adhesion on resin specimens was examined with scanning electron microscopy. Degree of conversion was studied with Fourier Transform Infrared Spectroscopy (FTIR). Flexural strength, microhardness and surface roughness was evaluated using a universal testing machine, microhardness tester and optical profilometer, respectively. Results. Incorporation of NAC into PMMA resin significantly reduced its cytotoxicity and enhanced cell adhesion on its surface. NAC induced negative influences on the mechanical and physical properties of PMMA resin in a dose-dependent manner. The degree of conversion for all experimental PMMA resins reached as high as 72% after 24 h of polymerization. All the tested properties were maintained when the concentration of incorporated NAC was 0.15 wt.%. Conclusion. The addition of 0.15 wt.% NAC remarkably improved biocompatibility of PMMA resin without exerting significant negative influence on its mechanical and physical properties. PMID:25922788

  17. Thermal cycling effects on adhesion of resin-bovine enamel junction among different composite resins.

    PubMed

    Chen, Wen-Cheng; Ko, Chia-Ling; Wu, Hui-Yu; Lai, Pei-Ling; Shih, Chi-Jen

    2014-10-01

    Thermal cycling is used to mimic the changes in oral cavity temperature experienced by composite resins when used clinically. The purpose of this study is to assess the thermal cycling effects of in-house produced composite resin on bonding strength. The dicalcium phosphate anhydrous filler surfaces are modified using nanocrystals and silanization (w/NP/Si). The resin is compared with commercially available composite resins Filtek Z250, Z350, and glass ionomer restorative material GIC Fuji-II LC (control). Different composite resins were filled into the dental enamel of bovine teeth. The bond force and resin-enamel junction graphical structures of the samples were determined after thermal cycling between 5 and 55C in deionized water for 600 cycles. After thermal cycling, the w/NP/Si 30wt%, 50wt% and Filtek Z250, Z350 groups showed higher shear forces than glass ionomer GIC, and w/NP/Si 50wt% had the highest shear force. Through SEM observations, more of the fillings with w/NP/Si 30wt% and w/NP/Si 50wt% groups flowed into the enamel tubule, forming closed tubules with the composite resins. The push-out force is proportional to the resin flow depth and uniformity. The push-out tubule pore and resin shear pattern is the most uniform and consistent in the w/NP/Si 50wt% group. Accordingly, this developed composite resin maintains great mechanical properties after thermal cycling. Thus, it has the potential to be used in a clinical setting when restoring non-carious cervical lesions. PMID:25047352

  18. Classification of natural resins by liquid chromatography-mass spectrometry and gas chromatography-mass spectrometry using chemometric analysis.

    PubMed

    Rhourrhi-Frih, B; West, C; Pasquier, L; Andr, P; Chaimbault, P; Lafosse, M

    2012-09-21

    Twenty-six resins from six botanical sources belonging to the class Magnoliopsida were compared based on gas chromatography-mass spectrometry and liquid chromatography-mass spectrometry data. The extracts were analysed by GC after silylation and by reversed phase LC combined with atmospheric pressure photoionisation (APPI) mass spectrometry. The chromatograms were re-organized in data matrices, where each sample was represented by a single column comprising 2755 observations (intensity, time, m/z) in GC-MS and 360 observations in LC-MS. A simple comparison of resin fingerprints was attempted by organizing data according to a three dimensional bubble chart (retention time against m/z where each point was a bubble which size represented the ion intensity) where it is possible to easily superimpose the fingerprints. Thus the common and different species can be easily observed enabling to classify the resins. Hierarchical cluster analysis based on characteristics of GC-MS and LC-MS profiles affords a complete description of the classes of the resins and shows that 26 resins are divided into five main clusters Commiphora mukul, Daniella oliveri, Gardenia gummifera, Canarium madagascariensis, Boswellia dalzielii and Boswellia serrata, respectively. In conclusion, the proposed method has been applied to three other resinous samples from the Burseraceae family to evaluate their alteration state. PMID:22885042

  19. Controversies in posterior composite resin restorations.

    PubMed

    Wilson, E G; Mandradjieff, M; Brindock, T

    1990-01-01

    The use of posterior composites is riddled with so many controversies that the puzzled practitioner must step warily among them. This modality is a minefield, where one careless movement can bring disaster. All composite restorations are subject to three big destructive forces--moisture, polymerization shrinkage, and clinical wear--forces that can eventually produce both microleakage and deterioration of the silane coupling agent linking filler particles to resin matrix. Despite the extreme technique sensitivity of posterior composite resins, knowledge of resin technology, sound operative dentistry principles and foresight in case selection can be effective in producing durable cosmetic restorations. Posterior composite resin restorations bonded to enamel and dentin reputedly strengthen teeth in both conventional and adhesive types of preparations provided polymerization shrinkage can be controlled. It is imperative that a knowledge of occlusal contacts be used to influence cavity outline, confining the trauma or occlusal forces away from the tooth-resin interface and helping to minimize occlusal wear. With the increased use of posterior resins, the trend in cavity preparations should break away from the traditional Black preparation toward the adhesive type preparation. If the Black Class II preparation is used, it is suggested that bevels be confined to the facial and lingual margins of the proximal box. Prewedging helps to maintain a conservative Class II preparation. Shade selection must be made prior to rubber dam isolation for greater accuracy and to help prevent postinsertion discoloration. The enamel should be pumiced to present a clean substrate for acid etching. The smear layer should be removed. The type of pulp protection applied before acid etching is dependent on the material used. After etching, the enamel should be washed with a 1 per cent potassium chloride solution. It is a more universally chemically stable solution than additive-laden local water supplies. The potassium chloride solution lowers the electrostatic forces on the enamel that would interfere with the flow of enamel bonding agents. Furthermore, tests have shown that the use of potassium chloride washes increase the strength of the enamel body by 40 per cent. Because of the depth of most posterior cavities, an incremental filling technique must be used to ensure a thorough polymerization of the resin and to forestall a massive polymerization shrinkage. When finished and contoured, the margins of the restoration should be re-etched, washed, and dried and then covered with an application of unfilled resin to discourage microleakage. Traditional operative dentistry technique must become flexible enough to meet the new demands of resin technology.(ABSTRACT TRUNCATED AT 400 WORDS) PMID:2403943

  20. Diffusion of residual monomer in polymer resins.

    PubMed Central

    Piver, W T

    1976-01-01

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

  1. Color stability of composite resin cements.

    PubMed

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

    2011-01-01

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

  2. 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.

  3. Polymerization characteristics of EMA-based resin.

    PubMed

    Saito, Yuji

    2004-03-01

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

  4. Isolation of novolak resin at low temperature

    NASA Astrophysics Data System (ADS)

    Rahman, M. D.; Aubin, Daniel P.; Khanna, Dinesh N.

    1996-06-01

    It is a well known fact that novolak resin undergoes chemical structure changes using vigorous synthesis conditions, such as under high acid catalyst loading and high temperature during isolation. Under such conditions, the structure of novolak resin is rearranged through quinone methide intermediate. We have also observed that the rearranged novolak resin does not perform well in photolithography. In this paper we discus the alternate isolation procedure, eliminating high temperature vacuum distillation. In this process a typical resin synthesis is performed using cresylic acids, catalyst and a solvent with the addition of formaldehyde over time. At the end of the condensation period, distillation is applied using a sub-surface high forced steam. Distillation is performed until all the unreacted cresols are removed. At this point the temperature is raised up to 140 degrees Celsius, and the vacuum is slowly drawn to 35 mm Hg to remove residual water. After the volatiles have been distilled off, the vacuum is released and a solvent is added to adjust the solid content. We discuss in this paper, the properties of the resin in the application of photolithography.

  5. 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

  6. Utilization of Methacrylates and Polymer Matrices for the Synthesis of Ion Specific Resins

    SciTech Connect

    Czerwinski, Kenneth

    2013-10-29

    Disposal, storage, and/or transmutation of actinides such as americium (Am) will require the development of specific separation schemes. Existing efforts focus on solvent extraction systems for achieving suitable separation of actinide from lanthanides. However, previous work has shown the feasibility of ion-imprinting polymer-based resins for use in ion-exchange-type separations with metal ion recognition. Phenolic-based resins have been shown to function well for Am-Eu separations, but these resins exhibited slow kinetics and difficulties in the imprinting process. This project addresses the need for new and innovative methods for the selective separation of actinides through novel ion-imprinted resins. The project team will explore incorporation of metals into extended frameworks, including the possibility of 3D polymerized matrices that can serve as a solid-state template for specific resin preparation. For example, an anhydrous trivalent f-element chain can be formed directly from a metal carbonate, and methacrylic acid from water. From these simple coordination complexes, molecules of discrete size or shape can be formed via the utilization of coordinating ligands or by use of an anionic multi-ligand system incorporating methacrylate. Additionally, alkyl methyl methacrylates have been used successfully to create template nanospaces, which underscores their potential utility as 3D polymerized matrices. This evidence provides a unique route for the preparation of a specific metal ion template for the basis of ion-exchange separations. Such separations may prove to be excellent discriminators of metal ions, even between f-elements. Resins were prepared and evaluated for sorption behavior, column properties, and proton exchange capacity.

  7. FluoMar™, a Fluorous Version of the Marshall Resin for Solution-Phase Library Synthesis

    PubMed Central

    Chen, Christine Hiu-Tung; Zhang, Wei

    2007-01-01

    The fluorous counterpart of the Marshall resin, 4-(1H,1H,2H,2H-perfluorodecylsulfanyl)phenol (FluoMar™) is prepared by S-alkylation of 4-mercaptophenol with C8F17CH2CH2I and employed in the synthesis of amide and diamide analogs. The final products are purified by solid-phase extraction (SPE) over FluoroFlash™ silica cartridges. PMID:12659562

  8. Identification of a resin-dentin hybrid layer in vital human dentin created in vivo: durable bonding to vital dentin.

    PubMed

    Nakabayashi, N; Ashizawa, M; Nakamura, M

    1992-02-01

    The present study investigated the bond of 5% 4-methacryloxyethyl trimellitate anhydride in methyl methacrylate, initiated by partially oxidized tri-n-butyl borane in the presence of poly(methyl methacrylate) powder, to vital human dentin. In vivo dentinal substrates were pretreated for 10 or 30 seconds with an aqueous solution of 10% citric acid and 3% ferric chloride. Transmission electron microscopic examination of the bonded cross sections revealed the formation of a transitional, or "hybrid," layer of resin-reinforced dentin created by the impregnation, co-mingling and envelopment of collagen bundles, and encapsulation of hydroxylapatite crystals. The in vivo adhesion was assumed to be durable, because results of microscopic examinations were comparable to those of durable bonding of the same resin to extracted bovine dentin. Vital dentin exhibited greater resistance to demineralization by the acid solution than do extracted teeth. Carious extracted teeth were more easily dissolved in acid than were noncarious extracted teeth. PMID:1322546

  9. 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

  10. The Creep of Laminated Synthetic Resin Plastics

    NASA Technical Reports Server (NTRS)

    Perkuhn, H

    1941-01-01

    The long-time loading strength of a number of laminated synthetic resin plastics was ascertained and the effect of molding pressure and resin content determined. The best value was observed with a 30 to 40 percent resin content. The long-time loading strength also increases with increasing molding pressure up to 250 kg/cm(exp 2); a further rise in pressure affords no further substantial improvement. The creep strength is defined as the load which in the hundredth hour of loading produces a rate of elongation of 5 X 10(exp -4) percent per hour. The creep strength values of different materials were determined and tabulated. The effect of humidity during long-term tests is pointed out.

  11. 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.

  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. 21 CFR 872.3200 - Resin tooth bonding agent.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3200 Resin tooth bonding agent. (a) Identification. A resin tooth bonding agent is a device material, such as methylmethacrylate, intended to be...

  14. 21 CFR 872.3200 - Resin tooth bonding agent.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3200 Resin tooth bonding agent. (a) Identification. A resin tooth bonding agent is a device material, such as methylmethacrylate, intended to be...

  15. 21 CFR 872.3200 - Resin tooth bonding agent.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3200 Resin tooth bonding agent. (a) Identification. A resin tooth bonding agent is a device material, such as methylmethacrylate, intended to be...

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

    PubMed

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

    2016-05-01

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

  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. 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

  19. 21 CFR 173.10 - Modified polyacrylamide resin.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... conditions: (a) The modified polyacrylamide resin is produced by the copolymerization of acrylamide with not... polyacrylamide resin contains not more than 0.05 percent residual acrylamide. (c) The modified...

  20. 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.

  1. 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.

  2. 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.

  3. Electronic structure and optical properties of resin.

    PubMed

    Rao, Zhi-Fan; Zhou, Rong-Feng

    2013-03-15

    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. PMID:23357580

  4. Resin Dermatitis in a Car Factory

    PubMed Central

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

    1966-01-01

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

  5. 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.

  6. 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

  7. 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.

  8. Development and validation of chemical and biological analyses to determine the antiestrogenic potency of resin acids in paper mill effluents.

    PubMed

    Terasaki, Masanori; Shiraishi, Fujio; Fukazawa, Hitoshi; Makino, Masakazu

    2009-12-15

    This study combined chemical analysis and bioassays of paper mill effluents and their components in order to determine their antiestrogenic activity. The bioassay comprised a yeast two-hybrid assay incorporating the estrogen receptor alpha (hERalpha) and an hERalpha competitive enzyme-linked immunosorbent assay (ELISA). Samples were fractionated by solid phase extraction (SPE) with a C18 disk and a Florisil cartridge to obtain four fractions. The final fraction, eluted with methanol from the Florisil cartridge after pre-extraction by the C18 disk, was the most active in the two-hybrid assay, and its antiestrogenic potency, expressed as the equivalent concentration to 4-hydroxytamoxifen (OHT), was 277 nM. Seven resin acids had antiestrogenic activity in the active fraction as determined by gas chromatography/mass spectrometry (GC/MS), and their concentration levels ranged from 0.11 to 12 microg/L. All the resin acids exhibited greater activity than OHT; their activity relative to OHT ranged from 2.8- to 4.0-fold in the yeast two-hybrid assay. Based on the chemical analysis data and relative potency of resin acids from the yeast two-hybrid assay, the contribution ratio of resin acids accounted for 72% of the observed antiestrogenic activity of the extract. Furthermore, no resin acid showed any affinity for the estrogen receptor in the ELISA. This study showed that analysis combining the SPE method and the yeast two-hybrid assay is likely to be effective for the comprehensive monitoring of resin acids in paper mill industrial discharge areas. PMID:20000523

  9. 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.

  10. 21 CFR 872.3690 - Tooth shade resin material.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

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

  11. 21 CFR 872.3690 - Tooth shade resin material.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

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

  12. 21 CFR 872.3690 - Tooth shade resin material.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

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

  13. 21 CFR 872.3670 - Resin impression tray material.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3670 Resin impression tray material. (a) Identification. Resin impression tray material is a device intended for use in a two-step dental mold fabricating... 21 Food and Drugs 8 2013-04-01 2013-04-01 false Resin impression tray material. 872.3670...

  14. 21 CFR 872.3690 - Tooth shade resin material.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

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

  15. 21 CFR 872.3690 - Tooth shade resin material.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

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

  16. 40 CFR 721.2673 - Aromatic epoxide resin (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Aromatic epoxide resin (generic). 721... Substances § 721.2673 Aromatic epoxide resin (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as aromatic epoxide resin (PMN...

  17. 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...

  18. 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...

  19. 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...

  20. Occupational asthma due to unheated polyvinylchloride resin dust.

    PubMed

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

    1989-11-01

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

  1. 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...

  2. 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...

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

    Code of Federal Regulations, 2013 CFR

    2013-07-01

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

  4. 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...

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

    Code of Federal Regulations, 2012 CFR

    2012-07-01

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

  6. 40 CFR 721.2752 - Epoxy resin containing phosphorus (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 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 721.2752 - 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...

  8. 40 CFR 721.9499 - Modified silicone resin.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Modified silicone resin. 721.9499... Substances § 721.9499 Modified silicone resin. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a modified silicone resin (PMN P-96-1649)...

  9. 40 CFR 721.9499 - Modified silicone resin.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Modified silicone resin. 721.9499... Substances § 721.9499 Modified silicone resin. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a modified silicone resin (PMN P-96-1649)...

  10. 40 CFR 721.9499 - Modified silicone resin.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Modified silicone resin. 721.9499... Substances § 721.9499 Modified silicone resin. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a modified silicone resin (PMN P-96-1649)...

  11. 40 CFR 721.9499 - Modified silicone resin.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Modified silicone resin. 721.9499... Substances § 721.9499 Modified silicone resin. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a modified silicone resin (PMN P-96-1649)...

  12. 21 CFR 872.3310 - Coating material for resin fillings.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

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

  13. 40 CFR 721.9499 - Modified silicone resin.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

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

  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, 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)...

  16. 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)...

  17. 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)...

  18. 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)...

  19. 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...

  20. 40 CFR 721.3135 - Phosphorous modified epoxy resin (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

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

  1. 40 CFR 721.2755 - Cycloaliphatic epoxy resin (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

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

  2. 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...

  3. 40 CFR 721.3135 - Phosphorous modified epoxy resin (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

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

  4. 40 CFR 721.3135 - Phosphorous modified epoxy resin (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

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

  5. 40 CFR 721.2755 - Cycloaliphatic epoxy resin (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

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

  6. 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...

  7. 40 CFR 721.2755 - Cycloaliphatic epoxy resin (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

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

  8. 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...

  9. 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...

  10. 21 CFR 177.2355 - Mineral reinforced nylon resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

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

  11. 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...

  12. 21 CFR 177.2355 - Mineral reinforced nylon resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Mineral reinforced nylon resins. 177.2355 Section... Repeated Use § 177.2355 Mineral reinforced nylon resins. Mineral reinforced nylon resins identified in... accordance with the following prescribed conditions: (a) For the purpose of this section the...

  13. 21 CFR 177.2355 - Mineral reinforced nylon resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

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

  14. 21 CFR 177.2355 - Mineral reinforced nylon resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

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

  15. 49 CFR 173.165 - Polyester resin kits.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... Polyester resin kits. (a) Except for transportation by aircraft, polyester resin kits consisting of a base... component and the organic peroxide component may be packed in the same strong outer packaging provided they... resin kits consisting of a base material component (Class 3, Packing Group II or III) and an...

  16. 21 CFR 872.3200 - Resin tooth bonding agent.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Resin tooth bonding agent. 872.3200 Section 872...) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3200 Resin tooth bonding agent. (a) Identification. A resin tooth bonding agent is a device material, such as methylmethacrylate, intended to be...

  17. 21 CFR 872.3200 - Resin tooth bonding agent.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

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

  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. 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...

  20. 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...

  1. 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...

  2. 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...

  3. 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...

  4. 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...

  5. 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...

  6. 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...

  7. 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...

  8. 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...

  9. 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...

  10. 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...

  11. 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...

  12. 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...

  13. 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...

  14. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food Additive Listing § 573.120 Acrylamide-acrylic acid resin. Acrylamide-acrylic acid resin... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Acrylamide-acrylic acid resin. 573.120 Section...

  15. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food Additive Listing § 573.120 Acrylamide-acrylic acid resin. Acrylamide-acrylic acid resin... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Acrylamide-acrylic acid resin. 573.120 Section...

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

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS Food Additive Listing § 573.120 Acrylamide-acrylic acid resin. Acrylamide-acrylic acid resin... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Acrylamide-acrylic acid resin. 573.120 Section...

  17. 21 CFR 872.3820 - Root canal filling resin.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

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

  18. 21 CFR 872.3820 - Root canal filling resin.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

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

  19. 21 CFR 872.3820 - Root canal filling resin.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

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

  20. 21 CFR 872.3300 - Hydrophilic resin coating for dentures.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

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

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

    Code of Federal Regulations, 2010 CFR

    2010-04-01

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

  2. 21 CFR 872.3300 - Hydrophilic resin coating for dentures.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

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

  3. 21 CFR 872.3300 - Hydrophilic resin coating for dentures.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

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

  4. 21 CFR 872.3300 - Hydrophilic resin coating for dentures.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

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

  5. 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...

  6. 21 CFR 173.5 - Acrylate-acrylamide resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Acrylate-acrylamide resins. 173.5 Section 173.5... CONSUMPTION Polymer Substances and Polymer Adjuvants for Food Treatment § 173.5 Acrylate-acrylamide resins. Acrylate-acrylamide resins may be safely used in food under the following prescribed conditions: (a)...

  7. 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...

  8. 21 CFR 177.2510 - Polyvinylidene fluoride resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

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

  9. 21 CFR 177.2510 - Polyvinylidene fluoride resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

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

  10. 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...

  11. Occupational asthma due to unheated polyvinylchloride resin dust.

    PubMed Central

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

    1989-01-01

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

  12. ELUTION OF URANIUM VALUES FROM ION EXCHANGE RESINS

    DOEpatents

    Kennedy, R.H.

    1959-11-24

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

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

    Code of Federal Regulations, 2012 CFR

    2012-04-01

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

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

    Code of Federal Regulations, 2014 CFR

    2014-04-01

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

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

    Code of Federal Regulations, 2011 CFR

    2011-04-01

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

  16. 21 CFR 872.3310 - Coating material for resin fillings.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

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

  17. Synthesis/characterization of a new chelating resin and on-line solid phase extraction for the determination of Ag(I) and Pd(II) from water, cream, anode slime and converter samples by flow injection flame atomic absorption spectrometry.

    PubMed

    Çetin, Tülin; Tokalioğlu, Serife; Ülgen, Ahmet; Sahan, Serkan; Özentürk, Ismail; Soykan, Cengiz

    2013-02-15

    On-line preconcentration procedures for the determination of Ag(I) and Pd(II) by flame atomic absorption spectrometry have been described. A new chelating resin, poly (N,N'-dipropionitrilemethacrylamide-co-divinylbenzene-co-2-acrylamido-2-methyl-1-propane sulfonic acid) was synthesized and used as a new adsorbent material. The resin was characterized by Fourier transform infrared spectroscopy and elemental analysis. Ag(I) was adsorbed on the chelating resin at pH 5.0 and eluted with 1.0 mol L(-1) HNO3. Pd(II) was retained at pH 9.5 and eluted with 1.5 mol L(-1) HCl. The experimental parameters (pH, type and concentration of eluent, flow rates of sample and eluent solutions, elution time and the effect of interfering ions) for both Ag(I) and Pd(II) were investigated in detail. The detection limit for Ag(I) was 2.4 μg L(-1) and the relative standard deviation was 2.9% for 0.2 μg mL(-1) Ag(I). The detection limit for Pd(II) was 1.7 μg L(-1) and the relative standard deviation was 2.8% for 0.3 μg mL(-1) Pd(II). Accuracy was confirmed by analyzing a certified reference material (TMDA-70), recovery studies on real samples and comparison with electrothermal atomic absorption analysis. The proposed methods were successfully applied to the on-line determination of Ag(I) in bottled water, pharmaceutical cream and anode slime samples and Pd(II) in bottled water and catalytic converter samples. PMID:23598028

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

    NASA Technical Reports Server (NTRS)

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

    2007-01-01

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

  19. Refining of fossil resin flotation concentrate from Western coal. Ninth quarterly report, January 1--March 31, 1995

    SciTech Connect

    Jensen, G.F.; Miller, J.D.

    1995-03-31

    Heptane showed a consistently higher extraction than hexane even through heptane contains only one more methylene group in its molecular structure. However economic factors must also be considered in the overall evaluation of the process. In this regard a simple economic evaluation was carried out taking into consideration the operating costs for the resin concentrate refining process. First of all, the price of industrial grade heptane is about the same as hexane. Because the process operates in a recycle mode, the initial cost would be about the same for both solvents. But in order to obtain the final resin product, the extracted resin has to be recovered from solution using evaporation techniques, which consume energy. Due to the significant difference in boiling points between the two solvents, approximately 25--35% more energy will be required for resin recovery by evaporation if heptane is used as the solvent for extraction. This represents a very significant increase of the operating cost. Secondly, based on bench scale tests the same yield can be achieved with hexane if the average residence time is increased. Such an increase in retention time only increases the capital cost by a small amount. It appears then from an economic perspective that hexane is the most appropriate solvent.

  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. 21 CFR 177.1556 - Polyaryletherketone resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 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 acid... water, 50 percent (by volume) ethyl alcohol in distilled water, 3 percent acetic acid (by weight)...

  2. Pharmaceutical Applications of Ion-Exchange Resins

    ERIC Educational Resources Information Center

    Elder, David

    2005-01-01

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

  3. 21 CFR 177.1550 - Perfluorocarbon resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... sealed source, at a maximum dose of gamma radiation not to exceed 7.5 megarads, or an electron beam at... articles intended for repeated use in contact with food. (d) Specifications—(1) Infrared identification. Perfluorocarbon resins can be identified by their characteristic infrared spectra. (2) Melt-viscosity. (i) The...

  4. 21 CFR 177.1550 - Perfluorocarbon resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... sealed source, at a maximum dose of gamma radiation not to exceed 7.5 megarads, or an electron beam at... articles intended for repeated use in contact with food. (d) Specifications—(1) Infrared identification. Perfluorocarbon resins can be identified by their characteristic infrared spectra. (2) Melt-viscosity. (i) The...

  5. 21 CFR 177.1550 - Perfluorocarbon resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... dose of gamma radiation not to exceed 7.5 megarads, or an electron beam at energy levels not to exceed... for repeated use in contact with food. (d) Specifications—(1) Infrared identification. Perfluorocarbon resins can be identified by their characteristic infrared spectra. (2) Melt-viscosity. (i) The...

  6. 21 CFR 177.1500 - Nylon resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Nylon resins. 177.1500 Section 177.1500 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces...

  7. 21 CFR 177.1330 - Ionomeric resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

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

  8. 21 CFR 177.1330 - Ionomeric resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

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

  9. 21 CFR 172.280 - Terpene resin.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Terpene resin. 172.280 Section 172.280 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION...

  10. Epoxy resins produce improved plastic scintillators

    NASA Technical Reports Server (NTRS)

    Markley, F. W.

    1967-01-01

    Plastic scintillator produced by the substitution of epoxy resins for the commonly used polystyrene is easy to cast, stable at room temperature, and has the desirable properties of a thermoset or cross-linked system. Such scintillators can be immersed directly in strong solvents, an advantage in many chemical and biological experiments.

  11. 21 CFR 177.1556 - Polyaryletherketone resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyaryletherketone resins. 177.1556 Section 177.1556 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use...

  12. 21 CFR 177.1556 - Polyaryletherketone resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

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

  13. Crack propagation directions in unfilled resins.

    PubMed

    Baran, G; Sadeghipour, K; Jayaraman, S; Silage, D; Paul, D; Boberick, K

    1998-11-01

    Posterior composite restorative materials undergo accelerated wear in the occlusal contact area, primarily through a fatigue mechanism. To facilitate the timely development of new and improved materials, a predictive wear model is desirable. The objective of this study was to develop a finite element model enabling investigators to predict crack propagation directions in resins used as the matrix material in composites, and to verify these predictions by observing cracks formed during the pin-on-disc wear of a 60:40 BISGMA:TEGDMA resin and an EBPADMA resin. Laser confocal scanning microscopy was used to measure crack locations. Finite element studies were done by means of ABAQUS software, modeling a cylinder sliding on a material with pre-existing surface-breaking cracks. Variables included modulus, cylinder/material friction coefficient, crack face friction, and yield behavior. Experimental results were surprising, since most crack directions were opposite previously published observations. The majority of surface cracks, though initially orthogonal to the surface, changed direction to run 20 to 30 degrees from the horizontal in the direction of indenter movement. Finite element modeling established the importance of subsurface shear stresses, since calculations provided evidence that cracks propagate in the direction of maximum K(II)(theta), in the same direction as the motion of the indenter, and at an angle of approximately 20 degrees. These findings provide the foundation for a predictive model of sliding wear in unfilled glassy resins. PMID:9823724

  14. Resin Characterization in Cured Composite Materials

    NASA Technical Reports Server (NTRS)

    Young, P. R.; Chang, A.

    1985-01-01

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

  15. 21 CFR 177.1555 - Polyarylate resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Polyarylate resins. 177.1555 Section 177.1555 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic...

  16. 21 CFR 177.1555 - Polyarylate resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyarylate resins. 177.1555 Section 177.1555 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic...

  17. 21 CFR 177.1555 - Polyarylate resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

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

  18. 21 CFR 177.1555 - Polyarylate resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyarylate resins. 177.1555 Section 177.1555 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic...

  19. Studies on chemoviscosity modeling for thermosetting resins

    NASA Technical Reports Server (NTRS)

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

    1987-01-01

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

  20. 21 CFR 177.1500 - Nylon resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Nylon resins. 177.1500 Section 177.1500 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces...

  1. 21 CFR 177.1500 - Nylon resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Nylon resins. 177.1500 Section 177.1500 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces...

  2. 21 CFR 177.1585 - Polyestercarbonate resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...., September 20, 1985, which is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51... is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies are... polycarbonate resins complying with § 177.1580: Provided, That the substances are used in accordance with...

  3. 21 CFR 177.1585 - Polyestercarbonate resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ..., 1985, which is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies... is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies are...) Substances regulated in § 178.2010(b) of this chapter for use in polycarbonate resins complying with §...

  4. 21 CFR 177.1585 - Polyestercarbonate resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ...., September 20, 1985, which is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51... is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies are... polycarbonate resins complying with § 177.1580: Provided, That the substances are used in accordance with...

  5. 21 CFR 177.1585 - Polyestercarbonate resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...., September 20, 1985, which is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51... is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies are... polycarbonate resins complying with § 177.1580: Provided, That the substances are used in accordance with...

  6. 21 CFR 177.1585 - Polyestercarbonate resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...., September 20, 1985, which is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51... is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies are... polycarbonate resins complying with § 177.1580: Provided, That the substances are used in accordance with...

  7. 21 CFR 177.1595 - Polyetherimide resin.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyetherimide resin. 177.1595 Section 177.1595 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use...

  8. Effect of resin thickness on the microhardness and optical properties of bulk-fill resin composites

    PubMed Central

    Kim, Eun-Ha; Jung, Kyoung-Hwa; Son, Sung-Ae; Hur, Bock; Kwon, Yong-Hoon

    2015-01-01

    Objectives This study evaluated the effects of the resin thickness on the microhardness and optical properties of bulk-fill resin composites. Methods Four bulk-fill (Venus Bulk Fill, Heraeus Kulzer; SDR, Dentsply Caulk; Tetric N-Ceram Bulk Fill, Ivoclar vivadent; SonicFill, Kerr) and two regular resin composites (Charisma flow, Heraeus Kulzer; Tetric N-Ceram, Ivoclar vivadent) were used. Sixty acrylic cylindrical molds were prepared for each thickness (2, 3 and 4 mm). The molds were divided into six groups for resin composites. The microhardness was measured on the top and bottom surfaces, and the colors were measured using Commission Internationale d'Eclairage (CIE) L*a*b* system. Color differences according to the thickness and translucency parameters and the correlations between the microhardness and translucency parameter were analyzed. The microhardness and color differences were analyzed by ANOVA and Scheffe's post hoc test, and a student t-test, respectively. The level of significance was set to α = 0.05. Results The microhardness decreased with increasing resin thickness. The bulk-fill resin composites showed a bottom/top hardness ratio of almost 80% or more in 4 mm thick specimens. The highest translucency parameter was observed in Venus Bulk Fill. All resin composites used in this study except for Venus Bulk Fill showed linear correlations between the microhardness and translucency parameter according to the thickness. Conclusions Within the limitations of this study, the bulk-fill resin composites used in this study can be placed and cured properly in the 4 mm bulk. PMID:25984474

  9. Decomposition of Rare Earth Loaded Resin Particles

    SciTech Connect

    Voit, Stewart L; Rawn, Claudia J

    2010-09-01

    The Fuel Cycle R and D (FCR and D) program within the Department of Energy Office of Nuclear Energy (DOE-NE) is evaluating nuclear fuel cycle options, including once-through, modified open, and fully closed cycles. Each of these scenarios may utilize quite different fuel management schemes and variation in fuel types may include high thermal conductivity UO{sub 2}, thoria-based, TRISO, metal, advanced ceramic (nitride, carbide, composite, etc.), and minor actinide (MA) bearing fuels and targets. Researchers from the US, Europe, and japan are investigating methods of fabricating high-specific activity spherical particles for fuel and target applications. The capital, operating, and maintenance costs of such a fuel fabrication facility can be significant, thus fuel synthesis and fabrication processes that minimize waste and process losses, and require less footprint are desired. Investigations have been performed at the Institute for Transuranium Elements (ITU) and the French Atomic Energy Commission (CEA) studying the impact of americium and curium on the fuel fabrication process. proof of concept was demonstrated for fabrication of MA-bearing spherical particles, however additional development will be needed for engineering scale-up. Researchers at the Paul Scherer Institute (PSI) and the Japan Atomic Energy Association (JAEA) have collaborated on research with ceramic-metallic (CERMET) fuels using spherical particles as the ceramic component dispersed in the metal matrix. Recent work at the CEA evaluates the burning of MA in the blanket region of sodium fast reactors. There is also interest in burning MA in Canada Deuterium Uranium (CANDU) reactors. The fabrication of uranium-MA oxide pellets for a fast reactor blanket or MA-bearing fuel for CANDU reactors may benefit from a low-loss dedicated footprint for producing MA-spherical particles. One method for producing MA-bearing spherical particles is loading the actinide metal on a cation exchange resin. The AG-50W resin is made of sulfonic acid functional groups attached to a styrene divinylbenzene copolymer lattice (long chained hydrocarbon). The metal cation binds to the sulfur group, then during thermal decomposition in air the hydrocarbons will form gaseous species leaving behind a spherical metal-oxide particle. Process development for resin applications with radioactive materials is typically performed using surrogates. For americium and curium, a trivalent metal like neodymium can be used. Thermal decomposition of Nd-loaded resin in air has been studied by Hale. Process conditions were established for resin decomposition and the formation of Nd{sub 2}O{sub 3} particles. The intermediate product compounds were described using x-ray diffraction (XRD) and wet chemistry. Leskela and Niinisto studied the decomposition of rare earth (RE) elements and found results consistent with Hale. Picart et al. demonstrated the viability of using a resin loading process for the fabrication of uranium-actinide mixed oxide microspheres for transmutation of minor actinides in a fast reactor. For effective transmutation of actinides, it will be desirable to extend the in-reactor burnup and minimize the number of recycles of used actinide materials. Longer burn times increases the chance of Fuel Clad Chemical or Mechanical Interaction (FCCI, FCMI). Sulfur is suspected of contributing to Irradiation Assisted Stress Corrosion Cracking (IASCC) thus it is necessary to maximize the removal of sulfur during decomposition of the resin. The present effort extends the previous work by quantifying the removal of sulfur during the decomposition process. Neodymium was selected as a surrogate for trivalent actinide metal cations. As described above Nd was dissolved in nitric acid solution then contacted with the AG-50W resin column. After washing the column, the Nd-resin particles are removed and dried. The Nd-resin, seen in Figure 1 prior to decomposition, is ready to be converted to Nd oxide microspheres.

  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. Resin systems for producing polymer concrete

    SciTech Connect

    Kukacka, L.E.

    1988-09-01

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

  12. Extraction of cesium from an alkaline leaching solution of spent catalysts using an ion-exchange column

    SciTech Connect

    Dumont, N.; Favre-Reguillon, A.; Dunjic, B.; Lemaire, M.

    1996-04-01

    The selective extraction of cesium from an alkaline leaching solution of spent catalysts using phenolic resins was studied. The resins were synthesized by alkaline polycondensation of formaldehyde by phenol, resorcinol, catechol, and phloroglucinol. Their ionoselectivities for five alkali metals were evaluated with a solid-liquid extraction, and their ion-exchange capacities were compared. The resin with the best selectivity for cesium was tested with a real solution at different pH values. An on-column extraction is proposed to obtain cesium with high purity.

  13. NITRATE CONVERSION OF HB-LINE REILLEXTM HPQ RESIN

    SciTech Connect

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

    2012-05-29

    Reillex{trademark} HPQ ion exchange resin is used by HB Line to remove plutonium from aqueous streams. Reillex{trademark} HPQ resin currently available from Vertellus Specialties LLC is a chloride ionic form, which can cause stress corrosion cracking in stainless steels. Therefore, HB Line Engineering requested that Savannah River National Laboratory (SRNL) convert resin from chloride form to nitrate form in the Engineering Development Laboratory (EDL). To perform this task, SRNL treated two batches of resin in 2012. The first batch of resin from Reilly Industries Batch 80302MA was initially treated at SRNL in 2001 to remove chloride. This batch of resin, nominally 30 liters, has been stored wet in carboys since that time until being retreated in 2012. The second batch of resin from Batch 23408 consisted of 50 kg of new resin purchased from Vertellus Specialties in 2012. Both batches were treated in a column designed to convert resin using downflow of 1.0 M sodium nitrate solution through the resin bed followed by rinsing with deionized water. Both batches were analyzed for chloride concentration, before and after treatment, using Neutron Activation Analysis (NAA). The resin specification [Werling, 2003] states the total chlorine and chloride concentration shall be less than 250 ppm. The resin condition for measuring this concentration is not specified; however, in service the resin would always be fully wet. Measurements in SRNL showed that changing from oven dry resin to fully wet resin, with liquid in the particle interstices but no supernatant, increases the total weight by a factor of at least three. Therefore, concentration of chlorine or chloride expressed as parts per million (ppm) decreases by a factor of three. Therefore, SRNL recommends measuring chlorine concentration on an oven dry basis, then dividing by three to estimate chloride concentration in the fully wet condition. Chloride concentration in the first batch (No.80302MA) was nearly the same before the current treatment (759 ppm dry) and after treatment (745 ppm dry or {approx}248 ppm wet). Treatment of the second batch of resin (No.23408) was very successful. Chloride concentration decreased from 120,000 ppm dry to an average of 44 ppm dry or {approx}15ppm wet, which easily passes the 250 ppm wet criterion. Per guidance from HB Line Engineering, SRNL blended Batch 80302 resin with Batch P9059 resin which had been treated previously by ResinTech to remove chloride. The chloride concentrations for the two drums of Batch P9059 were 248 ppm dry ({approx}83 ppm wet) {+-}22.8% and 583 ppm dry ({approx}194 ppm wet) {+-} 11.8%. The blended resin was packaged in five gallon buckets.

  14. Resin film infusion mold tooling and molding method

    NASA Technical Reports Server (NTRS)

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

    1999-01-01

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

  15. 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.

  16. The effect of polymerization conditions on the amounts of unreacted monomer and bisphenol A in dental composite resins.

    PubMed

    Kwon, Ha-Jeong; Oh, Yoon-Jong; Jang, Jong-Hwa; Park, Jung-Eun; Hwang, Kyung-Suk; Park, Yong-Duk

    2015-01-01

    The aim of this study was to analyze the unreacted monomers of four commonly used composite resins, which were released after curing with different polymerization conditions. Four composite resins, consisting of two hybrid types and two flowable types from two manufacturers, were photopolymerized using different curing times and curing distances. After polymerization, samples were extracted for analysis at different time points up to 24 h. Released monomers were analyzed by reversed-phase liquid chromatography at UV 210 nm. Longer curing times and shorter curing distances resulted in higher polymerization rates and decreased release of TEGDMA and UDMA, but changes in curing time and distance had no significant effect on Bis-GMA. Release of BPA increased with increase in curing time or decrease in curing distance, in contrast to the results of TEGDMA and UDMA. Polymerization conditions need to be differently applied according to both monomer and resin types. PMID:25904171

  17. Synthesis and Characterizations of Melamine-Based Epoxy Resins

    PubMed Central

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

    2013-01-01

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

  18. Electrically conductive resinous bond and method of manufacture

    DOEpatents

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

    1985-01-01

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

  19. Technique for removing resin from a molded object

    NASA Technical Reports Server (NTRS)

    Hemmi, I.; Morishita, T.; Ono, T.

    1983-01-01

    Resin is removed from a molded object in such a way that no cracks or expansion occurs in the casting. The resin is first mixed with a ceramics powder or metal powder. This mixture is then molded and the resin is removed by heat. The molded object is then placed into a container which is sealed and large enough to allow the gas from the resin to be controlled by heat from the resin. The gas pressure at the surface of the object is increased by the gas pressure generated from the resin and the resin removed. The increase in gas pressure from the surface of the molded object is 1.5 atm to 3 atm at 350 C to 400 C.

  20. Electrically conductive resinous bond and method of manufacture

    DOEpatents

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

    1987-01-01

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

  1. Effect of dentin dehydration and composite resin polymerization mode on bond strength of two self-etch adhesives

    PubMed Central

    Samimi, Pooran; Alizadeh, Mehdi; Shirban, Farinaz; Davoodi, Amin; Khoroushi, Maryam

    2016-01-01

    Background: Dual-cured composite resins are similar to self-cured composite resins in some of their clinical applications due to inadequate irradiation, lack of irradiation, or delayed irradiation. Therefore, incompatibility with self-etch adhesives (SEAs) should be taken into account with their use. On the other, the extent of dentin dehydration has a great role in the quality of adhesion of these resin materials to dentin. The aim of this study was to investigate the effect of dentin dehydration and composite resin polymerization mode on bond strength of two SEAs. Materials and Methods: A total of 120 dentinal specimens were prepared from extracted intact third molars. Half of the samples were dehydrated in ethanol with increasing concentrations. Then Clearfil SE Bond (CSEB) and Prompt L-Pop (PLP) adhesives were applied in the two groups. Cylindrical composite resin specimens were cured using three polymerization modes: (1) Immediate light-curing, (2) delayed light-curing after 20 min, and (3) self-curing. Bond strength was measured using universal testing machine at a crosshead speed of 1 mm/min. Data were analyzed with two-way ANOVA and Duncan post hoc tests. Statistical significance was defined at P < 0.05. Results: There were no significant differences for CSEB subgroups with hydrated and dehydrated dentin samples between the three different curing modes (P > 0.05). PLP showed significant differences between subgroups with the lowest bond strength in hydrated dentin with delayed light-curing and self-cured mode of polymerization. Conclusion: Within the limitations of this study, a delay in composite resin light-curing or using chemically cured composite resin had a deleterious effect on dentin bond strength of single-step SEAs used in the study. PMID:27041894

  2. Effect of light-curing units on microleakage under dental composite resins

    NASA Astrophysics Data System (ADS)

    Queiroz, R. S.; Bandéca, M. C.; Calixto, L. R.; Saade, E. G.; Nadalin, M. R.; Andrade, M. F.; Porto-Neto, S. T.

    2009-09-01

    The aim of this study was to determine the effect of two light-curing units (QTH and LED) on microleakage of Class II composite resin restorations with dentin cavosurface margins. Twenty extracted mandibular first premolars, free of caries and fractures were prepared two vertical “slot” cavities in the occluso-mesial and -destal surfaces (2 mm buccal-lingually, 2 mm proximal-axially and cervical limit in enamel) and divided into 4 equal groups ( n = 8): GI and GII: packable posterior composite light-activated with LED and QTH, respectively; GIII and GIV: micro-hybrid composite resin light-activated with LED and QTH, respectively. The composite resins were applied following the manufacturer’s instructions. After 24 h of water storage specimens were subjected to thermocycling for a total of 500 cycles at 5 and 55°C and the teeth were then sealed with impermeable material. Teeth were immersed in 0.5% Basic fuchsin during 24 h at room temperature, and zero to three levels of penetration score were attributed. The Mann-Whitney and Kruskal-Wallis tests showed significant statistically similar ( P > 0.05) from GI to GII and GIII to GIV, which the GII (2.750) had the highest mean scores and the GIII and GIV (0.875) had lowest mean scores. The use of different light-curing units has no influence on marginal integrity of Class II composite resin restorations and the proprieties of composite resins are important to reduce the microleakage.

  3. Temperature change, dentinal fluid flow and cuspal displacement during resin composite restoration.

    PubMed

    Ratih, D N; Palamara, J E A; Messer, H H

    2007-09-01

    Dentin-bonding agents and resin composite materials typically require light activation for polymerization. Light curing generates heat, which may influence dentinal fluid flow (DFF) and cuspal displacement. This study investigated the relationship among temperature increase, DFF and cuspal displacement in extracted human maxillary premolars with a mesial occlusal distal (MOD) cavity preparation. Two types of curing light were compared. Temperature changes were measured using thermocouples located on the occlusal cavity floor and at the pulp-dentine junction, during polymerization of bonding agent and resin composite material. DFF and cuspal displacement were measured simultaneously using automated flow measurement apparatus and direct current differential transformers respectively. Temperature increases of up to 15 degrees C were recorded during the restoration procedures. A quartz tungsten halogen (QTH) unit produced a significantly greater temperature increase than a light-emitting diode unit and curing of the bonding agent generated less temperature increase than curing of the resin composite. Heating due to exothermic reaction during polymerization of bonding agent and resin was not significantly different between light sources or between bonding and curing (P > 0.05). The QTH unit produced both greater inward fluid flow and cuspal displacement during the irradiation of bonding agent and resin composite than the light-emitting diode unit. There was not a simple relationship between temperature increase, fluid movement and cuspal displacement. From a clinical point of view, the light-emitting diode unit can be considered preferable to the QTH light, because it caused significantly smaller temperature increase, fluid shift and cuspal displacement. PMID:17716269

  4. Infiltration of natural caries lesions with experimental resins differing in penetration coefficients and ethanol addition.

    PubMed

    Meyer-Lueckel, H; Paris, Sebastian

    2010-01-01

    Resin infiltration of enamel caries lesions requires materials optimized for penetration into the capillary structures of the lesion body. With increasing penetration coefficients (PC) improved penetration and caries-inhibiting properties of low-viscosity resins (infiltrants) could be observed in artificial caries lesions. The aim of the present in vitro study was to compare the penetrativity of experimental resins varying in PC and ethanol addition into natural caries lesions using this technique. Extracted human molars and premolars showing proximal white spot lesions (International Caries Detection and Assessment System: code 2) were etched for 2 min using 15% hydrochloric acid gel. After drying, the lesions were stained with tetramethylrhodamine isothiocyanate and 1 of 4 experimental resins (PC63; PC185; PC204; PC391) was applied for 5 min. The materials consisted of bisphenol-A-glycidyl-methacrylate (B), tri-ethylene-glycol-dimethacrylate (T) and ethanol (E) in ratios (B:T:E) of PC63: 25:75:0; PC185: 20:60:20; PC204: 0:100:0; PC391: 0:80:20. Excess material was removed before light curing. The teeth were sectioned perpendicularly to the lesion surfaces and unbound dye was bleached by immersion in hydrogen peroxide. The remaining lesion pores were stained with fluorescein solution. Lesion and penetration depths were analyzed using confocal microscopy (n = 60). At deep lesion sites the percentage penetration of PC204 was significantly higher compared to PC63 and PC391 (p < 0.05; Mann-Whitney test) but only slightly higher than PC185 (p > 0.05). It can be concluded that materials with high PC (infiltrants) are capable of penetrating almost completely into enamel parts of natural caries lesions in vitro. A solvent-free resin mainly consisting of triethylene glycol dimethacrylate seems to be preferable. PMID:20714153

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

    SciTech Connect

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

    2010-12-01

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

  6. Salivary contamination and post-cured resin/resin lute bond.

    PubMed

    Stokes, A N; Pereira, B P

    1994-01-01

    A previous study has shown that sandblasting and silane priming a post-cured inlay resin gave a secure bond to dual-cure luting resin. To determine the influence of salivary contamination 4 additional groups of 15 post-cured resin discs were mounted in acrylic cylinders, their faces sandblasted with 50 microns alumina and silane primed. Surface treatments with saliva (sa), air/water spray (a/w), phosphoric acid gel (pa), and silane (si) followed in the order listed: A) control, no further treatment; B) sa, a/w; C) sa, a/w, si; D) sa, a/w, pa a/w; E) sa, a/w, pa, a/w, si. A 3.9 mm diameter column of dual-cure resin lute was then bonded to the dry stored in water surfaces. Specimens were stored in water for 2 weeks after which the dual-cure resin columns were sheared off the post-cured resin discs. Shear bond strengths were A) 19.2 +/- 3.7, B) 17.4 +/- 3.9, C) 16.7 +/- 3.1, D) 15.6 +/- 3.5, E) 15.4 +/- 2.3 MPa. One-way ANOVA and Duncan's Multiple Range Procedure showed groups D and E to be significantly lower than the uncontaminated control group A (p < 0.05). There were 2 adhesive failures in group B and all others were cohesive within the post-cured resin discs. This implies that air/water alone after salivary contamination is an unreliable cleansing method. The low shear bond values for Groups D and E may have been related to inadequate clearance of the phosphoric acid gel. It was concluded that salivary contamination adversely affected the quality of the bonds studied and decontamination using phosphoric acid gel resulted in significantly reduced shear bond strengths. PMID:9582676

  7. Preparative separation and purification of fumigaclavine C from fermented mycelia of Aspergillus fumigatus CY018 by macroporous adsorption resin.

    PubMed

    Yao, Ling-Yun; Zhu, Yi-Xiang; Liu, Chang-Qing; Jiao, Rui-Hua; Lu, Yan-Hua; Tan, Ren-Xiang

    2015-05-01

    In this work, the separation and purification of fumigaclavine C (FC), an ergot alkaloid with strong anti-inflammatory activity from fermented mycelia of Aspergillus fumigatus was systematically evaluated. Among the eight tested resins, the non-polar resin D101 displayed the best adsorption and desorption based on of static adsorption and desorption tests. Adsorption isotherms were constructed on D101 resin and fitted well to the Freundlich model. Dynamic adsorption and desorption tests on a column packed with D101 resin have been investigated for optimization of chromatographic parameters. Under optimized conditions, the contents of FC increased from 7.32% (w/w) in the crude extract to 67.54% in the final product with a recovery yield of 90.35% (w/w) via one run. Furthermore, a lab scale-up separation was carried out, in which the FC content and recovery yield were 65.83% and 90.13%, respectively. These results demonstrated that this adsorption-desorption strategy by using D101 resin was simple and efficient, thus showing potential for large scale purification and preparation of FC in the future. PMID:25817261

  8. 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.

  9. Evaluation of the biocompatibility of resin-based root canal sealers in rat periapical tissue.

    PubMed

    Mutoh, Noriko; Satoh, Takenori; Watabe, Hirotaka; Tani-Ishii, Nobuyuki

    2013-01-01

    We evaluated the biocompatibility of resin-based root canal sealers (RCSs) in the periapical tissues of rats. Wistar rats underwent tooth replantation for reproducing the response of periapical tissue with RCSs. The resin-based Epipany SE, AH Plus Jet, the eugenol-based sealer (Canals) and a control group were employed. The upper right first molar was extracted and applied with RCSs on apices, and then the tooth was repositioned. Histological evaluation demonstrated that mild inflammation occurred in the periapical tissue with Epiphany and AH Plus Jet sealers on day 7, whereas Canals induced severe-to-moderate inflammation. The statistical analyses demonstrated that the significant differences were observed between Canals and the other groups on day 7 regarding inflammatory response. On day 14, the lesions induced by all sealers were healed and replaced predominantly by fibrous connective tissue. Our results suggest that Epiphany SE and AH Plus Jet are good biocompatible materials. PMID:23719002

  10. Influence of endodontic materials on the bonding of composite resin to dentin.

    PubMed

    Macchi, R L; Capurro, M A; Herrera, C L; Cebada, F R; Kohen, S

    1992-02-01

    We assessed the bond strength of a composite resin to dentin that had been in contact with different materials. Flat dentin surfaces in freshly extracted human teeth were covered for 15 min or 48 h with a 1-mm layer of a variety of materials. The products were mechanically removed and a composite resin cylindrical specimen bonded to the dentin surface using the Prisma universal bond system. After 7 days immersion at 37 degrees C in water, the tensile bond strength was tested. The results were compared with those on dentin surfaces not in contact with any endodontic material. Statistical analysis showed that some materials (Grossmans Cement, IRM, Maisto's slowly resorbable paste) reduced the strength of the bond or even precluded bonding. It is necessary to develop techniques that will eliminate this when restoring endodontically treated teeth. PMID:1396358

  11. Ethynylated aromatics as high temperature matrix resins

    NASA Technical Reports Server (NTRS)

    Hurwitz, F. I.

    1987-01-01

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

  12. Flammability of Epoxy Resins Containing Phosphorus

    NASA Technical Reports Server (NTRS)

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

    2005-01-01

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

  13. Ethynylated aromatics as high temperature matrix resins

    NASA Technical Reports Server (NTRS)

    Hurwitz, Frances I.

    1986-01-01

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

  14. Fatigue properties of acrylic denture base resins.

    PubMed

    Fujii, K

    1989-12-01

    Observations were made of fractured surfaces caused by flexural and tensile fatigue tests made in polymethyl methacrylate denture base resins (PMMA). In addition, the changes in dynamic viscoelastic and tensile properties of the materials along with fatigue propagation were investigated. In the tensile and flexural fatigue tests, both the fractured surfaces, which had striations on their surfaces and cracks near the fractured section, closely resembled each other in appearance. On the other hand, all of the tensile properties, such as elastic modulus, toughness and tensile strength, decreased with the increase of the number of stress cycles in the fatigue test. The storage modulus (E') of the material decreased gradually along with fatigue propagation over the whole range of temperatures tested. The loss modulus (E") and mechanical loss tangent (tan delta) increased slightly. The fatigue limit of four commercial denture base resins varied widely from one product to another. PMID:2490598

  15. Epoxy resins in the construction industry.

    PubMed

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

    2006-09-01

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

  16. Pulsed laser photopolymerization of dental composite resins

    NASA Astrophysics Data System (ADS)

    Meniga, Andrej; Sutalo, Zrinka; Azinovic, Davorka; Pichler, Goran

    1993-12-01

    The aim of this investigation was to improve the quality of the cured composite resin using the pulsed laser, thus avoiding disadvantages of previously used methods. The light source consisted of the pump excimer laser (Lambda Physik LPX 100) and the dye laser (Lambda Physik 3000). It is expected that pulsed laser polymerization could improve the conversion rate, decrease a temperature rise in the sample, allowing the `cooling' of the material and reduce polymerization shrinkage.

  17. Ion Exchange Resins Transforming Drug Delivery Systems.

    PubMed

    Gupta, Shweta; Parul; Sahoo, P K

    2010-02-17

    Ion-exchange resins are light, porous, three-dimensional high molecular weight cross -linked matrix of hydrocarbon chains carrying positively or negatively charged sites that can attract an ion of opposite charge from the surrounding medium. There is stoichiometric exchange of mobile ions between the solid and the solution called as Ion-exchange which does not lead to any radical change in the properties and structure of the solid. Depending upon the type of Ion-exchanged it can be either Cation-exchange or Anion-exchange. They are prepared in the form of granules, beads or sheets. As drug delivery systems they have received considerable attention after the 1950s due to their inertness, freedom from side effects, high drug loading capacity, ease of sterilization and the fact that their structure can be easily altered to achieve the desired drug release characteristics. Their use is revolutionizing all traditional delivery systems namely- oral, nasal, ophthalmic and parenteral. Ion- exchange resins have been used for the development of novel drug delivery systems (NDDSs), to modify the characteristics of the dosage form and various other biomedical applications. The present article deals with the varied applications of ion-exchange resins for taste making, as resinates (simple and microencapsulated or coated), Pennkinetic systems, in selective recovery of pharmaceuticals, in pH and ionic strength responsive systems, in gastro-retentive systems, in hollow fiber systems, as sigmoidal release systems, as site specific delivery systems and as inotophoretically assisted transdermal drug delivery systems. They also have an immense importance when used as disintegrants / superdisintegrants in formulation of orodispersible tablets, powder processing aids and in the dissolution and stabilization of drugs. PMID:20158479

  18. Ion Exchange Resins Transforming Drug Delivery Systems.

    PubMed

    Gupta, Shweta; Benien, Parul; Sahoo, P K

    2010-07-01

    Ion-exchange resins are light, porous, three-dimensional high molecular weight cross - linked matrix of hydrocarbon chains carrying positively or negatively charged sites that can attract an ion of opposite charge from the surrounding medium. There is stoichiometric exchange of mobile ions between the solid and the solution called as Ion-exchange which does not lead to any radical change in the properties and structure of the solid. Depending upon the type of Ionexchanged it can be either Cation-exchange or Anion-exchange. They are prepared in the form of granules, beads or sheets. As drug delivery systems they have received considerable attention after the 1950s due to their inertness, freedom from side effects, high drug loading capacity, ease of sterilization and the fact that their structure can be easily altered to achieve the desired drug release characteristics. Their use is revolutionizing all traditional delivery systems namely - oral, nasal, ophthalmic and parenteral. Ion- exchange resins have been used for the development of novel drug delivery systems (NDDSs), to modify the characteristics of the dosage form and various other biomedical applications. The present article deals with the varied applications of ion-exchange resins for taste making, as resinates (simple and microencapsulated or coated), Pennkinetic systems, in selective recovery of pharmaceuticals, in pH and ionic strength responsive systems, in gastro-retentive systems, in hollow fiber systems, as sigmoidal release systems, as site specific delivery systems and as inotophoretically assisted transdermal drug delivery systems. They also have an immense importance when used as disintegrants / superdisintegrants in formulation of orodispersible tablets, powder processing aids and in the dissolution and stabilization of drugs. PMID:20497105

  19. Fire- and Heat-Resistant Laminating Resins

    NASA Technical Reports Server (NTRS)

    Kourtides, Demetrius A.; Mikroyannidis, John A.

    1987-01-01

    Imide compounds containing phosphourus thermally polymerized. New maleimido- or citraconimido-end-capped monomers, have relatively low melting temperatures, polymerized at moderate temperatures to rigid bisimide resins without elimination of volatiles. Monomers dissolve in such solvents as methyl ethyl ketone, acetone, and tetrahydrofuran, suitable and perferred as "varnish solvents" for composite fabrication. Low melting points of these componds allow use as adhesives without addition of solvents.

  20. Single Frequency Characterization of a Commercial Resin

    SciTech Connect

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

    2009-10-01

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

  1. Processable polyimide adhesive and matrix composite resin

    NASA Technical Reports Server (NTRS)

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

    1990-01-01

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

  2. Toward homogeneous nanostructured polyaniline/resin blends.

    PubMed

    Jafarzadeh, Shadi; Thormann, Esben; Rönnevall, Ted; Adhikari, Arindam; Sundell, Per-Erik; Pan, Jinshan; Claesson, Per M

    2011-05-01

    The high interest in applications of conducting polymers, especially polyaniline (PANI), makes it important to overcome limitations for effective usage due to poor processability and solubility. One promising approach is to make blends of PANI in polymeric resins. However, in this approach other problems related to the difficulty of achieving a homogeneous PANI dispersion arise. The present article is focused on this general problem, and we discuss how the synthesis method, choice of dopant and solvent as well as interfacial energies influence the dispersibility. For this purpose, different synthesis methods and dopants have been employed to prepare nanostructures of polyaniline. Dynamic light scattering analysis of dispersions of the synthesized particles in several solvents was employed in order to understand how the choice of solvent affects PANI aggregation. Further information on this subject was achieved by scanning electron microscopy studies of PANI powders dried from various solutions. On the basis of these results, acetone was found to be a suitable dispersion medium for PANI. The polymer matrix used to make the blends in this work is a UV-curing solvent-free resin. Therefore, there is no low molecular weight liquid in the system to facilitate the mixing process and promote formation of homogeneous dispersions. Thus, a good compatibility of the components becomes crucial. For this reason, surface tension and contact angle measurements were utilized for characterizing the surface energy of the PANI particles and the polyester acrylate (PEA) resin, and also for calculating the interfacial energy between these two components that revealed good compatibility within the PANI/PEA blend. A novel technique, based on centrifugal sedimentation analysis, was employed in order to determine the PANI particle size in PEA resin, and high dispersion stability of the PANI/PEA blends was suggested by evaluation of the sedimentation data. PMID:21480657

  3. Composites with improved fiber-resin interfacial adhesion

    NASA Technical Reports Server (NTRS)

    Cizmecioglu, Muzaffer (Inventor)

    1989-01-01

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

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

    SciTech Connect

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

    1994-01-01

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

  5. Composite fabrication via resin transfer molding technology

    SciTech Connect

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

    1996-04-01

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

  6. Surface integrity of provisional resin materials

    NASA Astrophysics Data System (ADS)

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

    2006-03-01

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

  7. Chemoviscosity modeling for thermosetting resins - I

    NASA Technical Reports Server (NTRS)

    Hou, T. H.

    1984-01-01

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

  8. Transparent resins for 157-nm lithography

    NASA Astrophysics Data System (ADS)

    Dammel, Ralph R.; Sakamuri, Raj; Romano, Andrew R.; Vicari, Richard; Hacker, Cheryl; Conley, Will; Miller, Daniel A.

    2001-08-01

    The development of sufficiently transparent resin systems is one of the key elements required for a successful and timely introduction for 157 nm lithography. This paper reports on the Simple Transmission Understanding and Prediction by Incremental Dilution (STUPID) model, a quick back-of-the-envelope increment scheme to estimate the absorption of polymers at 157 nm. A number of promising candidate resins based on norbornenes are discussed, and results with a first 157 nm resin system developed at the University of Austin are presented. The new system is based on copolymers of norbornene-5-methylenehexafluoroisopropanol (NMHFA) and t-butyl norbornene carboxylate (BNC), formulated with an acetal additive obtained by copolymerization of t-butyl norbornene-5-trifluoromethyl-5-carboxylate (BNTC) with carbon monoxide. Lithographic performance of this system extends to 110 nm dense features using standard illumination and a binary mask, or 80 nm semi-dense and 60 nm isolated features with a strong phase shift mask. The dry etch resistance of this resist is found to be slightly lower than APEX-E DUV resist for polysilicon but superior to it for oxide etches.

  9. Cytotoxicity of Resin Composites Containing Bioactive Glass Fillers

    PubMed Central

    Salehi, Satin; Gwinner, Fernanda; Mitchell, John C; Pfeifer, Carmem; Ferracane, Jack L

    2015-01-01

    Objective To determine the in vitro cytotoxicity of dental composites containing bioactive glass fillers. Methods Dental composites (50:50 Bis-GMA/TEGDMA resin: 72.5wt% filler, 67.5%Sr-glass and 5% OX50) containing different concentrations (0, 5, 10 and 15 wt %) of two sol-gel bioactive glasses, BAG65 (65 mole% SiO2, 31 mole% CaO, 4 mole% P2O5) and BAG62 (3 mole% F added) were evaluated for cytotoxicity using Alamar Blue assay. First, composite extracts were obtained from 7 day incubations of composite in cell culture medium at 37° C. Undifferentiated pulp cells (OD-21) were exposed to dilutions of the original extracts for 3, 5, and 7 days. Then freshly cured composite disks were incubated with OD-21 cells (n=5) for 2 days. Subsequently, fresh composite disks were incubated in culture medium at 37°C for 7 days, and then the extracted disks were incubated with OD-21 cells for 2 days. Finally, fresh composites disks were light cured for 3, 5, and 20 seconds and incubated with OD-21 cells (n=5) for 1, 3, 5, and 7 days. To verify that the three different curing modes produced different levels of degree of conversion (DC), the DC of each composite was determined by FTIR. Groups (n=5) were compared with ANOVA/Tukey’s (α≤0.05). Results Extracts from all composites significantly reduced cell viability until a dilution of 1:8 or lower, where the extract became equal to the control. All freshly-cured composites showed significantly reduced cell viability at two days. However, no reduction in cell viability was observed for any composite that had been previously soaked in media before exposure to the cells. Composites with reduced DC (3 s vs. 20 s cure), as verified by FTIR, showed significantly reduced cell viability. Significance The results show that the composites, independent of composition, had equivalent potency in terms of reducing the viability of the cells in culture. Soaking the composites for 7 days before exposing them to the cells suggested that the “toxic” components had been extracted and the materials were no longer cytotoxic. The results demonstrate that the cytotoxicity of composites with and without BAG must predominantly be attributed to the release of residual monomers, and not to the presence of the BAG. PMID:25564110

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

    NASA Technical Reports Server (NTRS)

    Alston, William B.

    1988-01-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2010-10-01

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

  12. 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.

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

    PubMed

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

    2015-04-01

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

  14. Conventional and microfilled composite resins. Part II. Chip fractures.

    PubMed

    Lambrechts, P; Ameye, C; Vanherle, G

    1982-11-01

    Dentists are accustomed to advantages and disadvantages in the materials at their disposal. This article was concerned with one disadvantage of microfilled composite resins, namely, chip fractures. Probably due to their higher coefficient of thermal expansion, higher water sorption, higher polymerization shrinkage, and lower tensile strengths, cohesive as well as adhesive chip fractures occur three to four times more often with microfilled composite resins than with conventional composite resins. Microfilled composite resins are indicated for esthetic purposes. They are contraindicated for Class IV and stress-bearing restorations. They are indicated for limited use in Class I restorations where esthetics is of primary importance. The technique of use must include acid-etching and intermediate bonding. The microfilled composite resins enjoy a smooth finish and high luster. This offers advantages in areas where smoothness is paramount. They may replace conventional composite resins for resurfacing existing restorations and veneering stained or mottled anterior teeth. They are indicated for treatment of cervical erosion. PMID:6958862

  15. Health Problems of Epoxy Resins and Amine-curing Agents

    PubMed Central

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

    1959-01-01

    Epoxy resins were first introduced about 10 years ago. Toxic effects, particularly dermatitis, have been frequently described. An investigation into the possible causes of pathological sequelae following the use of epoxy resin/amine mixtures has been undertaken. The cause of most cases of dermatitis and sensitization appears to be uncombined amine which is present in recent mixtures and persists in hardened resin for long periods. The results of experiments with two of the most commonly used resin/amine mixtures confirm this. Cold-cured resins are more dangerous and remain so even when hardened. A simple theory is suggested for the mechanism of the reaction between epoxy resins, amines, and biological systems. This theory leads logically to the handling precautions outlined. Images PMID:13651551

  16. Bismaleimide resins for flame resistant honeycomb sandwich panels

    NASA Technical Reports Server (NTRS)

    Stenzenberger, H. D.

    1978-01-01

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

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

    DOEpatents

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

    2011-03-29

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

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

    DOEpatents

    Huszagh, D.W.

    1984-01-01

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

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

    DOEpatents

    Huszagh, Donald W.

    1985-01-01

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

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

    DOEpatents

    Yamamori, Naoki; Yokoi, Junji; Yoshikawa, Motoyoshi

    1984-01-01

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