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Sample records for advanced polymer resins

  1. Advanced Polymer

    NASA Technical Reports Server (NTRS)

    1992-01-01

    In the mid-1980's, Langley developed a polyimide sulfone, combining desirable properties of two classes of polymers. Composites and other products made from polyimide sulfone can be used with solvents and corrosive fluids, are light weight, low cost and can be easily fabricated for a wide range of industrial uses. High Technology Systems, Inc. obtained a license for the polymer and was awarded a Small Business Innovation Research (SBIR) contract for development in a powder form. Although its principal use is as a matrix resin for composites, the material can also be used as a high temperature structural adhesive for aircraft structures and as a coating for protection from heat and radiation for electronic components.

  2. 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.

  3. 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

  4. Advanced thermoset resins for fire-resistant composites

    NASA Technical Reports Server (NTRS)

    Kourtides, D. A.; Parker, J. A.

    1979-01-01

    The thermal and flammability properties of some thermoset polymers and composites are described. The processing and evaluation of composites fabricated from currently used resins and advanced fire-resistant resins are also described. Laboratory test methodology used to qualify candidate composite materials includes thermochemical characterization of the polymeric compounds and evaluation of the glass reinforced composites for flammability and smoke evolution. The use of these test methods will be discussed in comparing advanced laminating resins and composites consisting of modified epoxies, phenolics and bismaleimide, with conventional baseline materials consisting of epoxy.

  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. Study of improved resins for advanced supersonic technology composites. Part 1: Heteroaromatic polymers containing ether groups. Part 2: Curing chemistry of aromatic polymers and composite studies

    NASA Technical Reports Server (NTRS)

    Takekoshi, T.; Hillig, W. B.; Mellinger, G. A.

    1975-01-01

    Fourteen ether-containing, aromatic dianhydrides have been synthesized from N-phenyl-3 or 4-nitrophthalimide and various bisphenols. The process involves nucleophilic displacement of activated nitro groups with bisphenolate ions. Ether-containing dianhydrides were indefinitely stable in the presence of atmospheric moisture. One-step, high temperature solution polymerization of the ether-containing dianhydrides with m-phenylene diamine, 4,4'-oxydianiline and 1, 3-bis(4-aminophenoxy)benzene afforded 42 polyetherimides. The polyetherimides were all soluble in m-cresol except two which were found to be crystalline. The glass transition temperatures of the polyetherimides ranged from 178 to 277 C. Soluble polybenzimidazopyrrolones containing ether groups were also prepared from the same ether-containing dianhydrides and aromatic tetraamines by one-step solution polymerization. Using low molecular weight polyetherimides, various thermoset resin systems were developed and tested as matrices for fiber-reinforced composites. The curing chemistry involving reaction of the phthalonitrile group and the o-diaminophenyl group was found to be generally applicable to crosslinking various aromatic polymers other than polyimides.

  7. 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.

  8. Bismaleimides and related maleimido polymers as matrix resins

    NASA Technical Reports Server (NTRS)

    Parker, J. A.; Kourtides, D. A.; Fohlen, G. M.

    1985-01-01

    Significant processing and property improvements can be achieved by copolymerization of state-of-the-art bisimides with various vinyl stilbazole derivatives to give both fire resistance and high-temperature properties from hot-melt compositions. Significant improvement in mechanical properties is achieved through these modifications, which may make these new matrix resins ideal candidates for fireworthy secondary graphite composite structures. Phosphorous modifications of maleimido polymers through phosphonate structure and tricyclophosphazene derivatives provide families of new matrix resins for short-time applications in severe thermo-oxidative environments. With further research these may provide matrix resins for long-term thermo-oxidative stability of advanced composites at temperatures up to 400 to 500 C.

  9. 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.

  10. 21 CFR 177.1650 - Polysulfide polymer-polyepoxy resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

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

  11. Electroactive polymer gels based on epoxy resin

    NASA Astrophysics Data System (ADS)

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

    2007-04-01

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

  12. Survey of inorganic polymers. [for composite matrix resins

    NASA Technical Reports Server (NTRS)

    Gerber, A. H.; Mcinerney, E. F.

    1979-01-01

    A literature search was carried out in order to identify inorganic, metallo-organic, and hybrid inorganic-organic polymers that could serve as potential matrix resins for advanced composites. The five most promising candidates were critically reviewed and recommendations were made for the achievement of their potential in terms of performance and cost. These generic polymer classes comprise: (1) Poly(arylsil sesquioxanes); (2) Poly(silyl arylene siloxanes); (3) Poly(silarylenes); (4) Poly(silicon-linked ferrocenes); and (5) Poly(organo phosphazenes). No single candidate currently possesses the necessary combination of physicomechanical properties, thermal stability, processability, and favorable economics. The first three classes exhibit the best thermal performance. On the other hand, poly (organo phosphazenes), the most extensively studied polymer class, exhibit the best combination of structure-property control, processability, and favorable economics.

  13. 21 CFR 177.1650 - Polysulfide polymer-polyepoxy resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polysulfide polymer-polyepoxy resins. 177.1650... (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1650 Polysulfide...

  14. 21 CFR 177.1650 - Polysulfide polymer-polyepoxy resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polysulfide polymer-polyepoxy resins. 177.1650 Section 177.1650 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...

  15. 21 CFR 177.1650 - Polysulfide polymer-polyepoxy resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polysulfide polymer-polyepoxy resins. 177.1650... (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1650 Polysulfide...

  16. Photonic metal-polymer resin nanocomposites with chiral nematic order.

    PubMed

    Zamarion, Vitor M; Khan, Mostofa K; Schlesinger, Maik; Bsoul, Anas; Walus, Konrad; Hamad, Wadood Y; MacLachlan, Mark J

    2016-06-14

    Mesoporous resins with chiral nematic order were used as scaffolds to construct novel iridescent metal-polymer composites. Gold, silver and palladium nanoparticles were formed by an in situ reduction reaction. We have investigated the effects of concentration and time on the deposition. As a proof-of-concept, we demonstrate that this process can be extended to patterning photonic resins by inkjet printing. PMID:27241485

  17. 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.

  18. Polymer-grafted silica: A screening system for polymeric adsorption resin development

    SciTech Connect

    Browne, T.E.; Cohen, Y. )

    1993-04-01

    A screening-level methodology was developed for the evaluation of solute affinity for polymers that are candidate sorption resins. In this approach novel grafted polymer-silica resins were synthesized to produce poly(vinylpyrrolidone)-silica (PVP-Si) and poly(vinyl acetate)-silica (PVAc-Si) resins. The polymer-silica resins along with a number of commercially available polymer resins were used to evaluate the aqueous-phase adsorption of phenol, tetrachloroethene (PCE), trichloroethene (TCE), and chloroform. The polymer-grafted silicas were able to selectively remove pollutants from water with a covalently bonded polymer layer that has a high affinity for the target pollutant. The PVAc-silica resin had a sorption capacity for TCE and CHCl[sub 3] as high as commercial poly(styrene) resin XAD-4; the PVP-Si resin had a sorption capacity for phenol higher than a commercial poly-(vinylpyridine) resin (Reillex 425). PCE adsorption onto the PVAc-silica was comparable to the commercial poly(methacrylate) and poly(vinylpyridine) resins but less than the poly(styrene) resin. The results show that the Hildebrand solubility parameter along with the dipole moment of the polymer functional groups can be used for an initial screening-level assessment of polymer-solute affinity.

  19. Advanced Polymer Processing Facility

    SciTech Connect

    Muenchausen, Ross E.

    2012-07-25

    Some conclusions of this presentation are: (1) Radiation-assisted nanotechnology applications will continue to grow; (2) The APPF will provide a unique focus for radiolytic processing of nanomaterials in support of DOE-DP, other DOE and advanced manufacturing initiatives; (3) {gamma}, X-ray, e-beam and ion beam processing will increasingly be applied for 'green' manufacturing of nanomaterials and nanocomposites; and (4) Biomedical science and engineering may ultimately be the biggest application area for radiation-assisted nanotechnology development.

  20. Polymer lasers: recent advances

    NASA Astrophysics Data System (ADS)

    Riedl, T.; Rabe, T.; Görrn, P.; Wang, J.; Weinmann, T.; Hinze, P.; Galbrecht, F.; Scherf, U.; Kowalsky, W.

    2007-09-01

    The development of organic thin film lasers has seen tremendous progress over the past few years. Only a few materials are necessary to allow for continuous wavelength tunability in the spectral region from the UV to the near IR. At the same time, the lasing thresholds of organic thin film lasers have been reduced considerably both due to improved low-loss distributed feedback (DFB) resonator structures and highly efficient gain materials based on guest-host energy transfer. Aside from the as yet open issue of electrical operation of organic lasers, which we will address briefly in this paper, there are numerous applications (e.g. in biotechnology, spectroscopy) where optically driven organic lasers may be the more cost effective and versatile solution. In this context, tunable polymer lasers pumped by compact and inexpensive InGaN laser diodes will be shown. These lasers are based on a modified poly(9,9'-dioctylfluorene) derivative (BN-PFO) containing 12% of -6,6'-(2,2'-octyloxy-1,1'-binaphthyl) spacer groups doped with a few wt% of the stilbene dye 1,4-Bis(2-(4-(N,N-di(p-tolyl)amino)phenyl)vinyl-benzene (DPAVB). With the same host polymer (BN-PFO) quasi continuous wave operation (up to 5 MHz) can be demonstrated. Highly repetitive lasers are especially desirable for many spectroscopic applications. This regime of operstion is found to be impeded by the photo-physics in doped organic systems where the accumulation of absorptive species in the gain medium leads to piled-up absorption losses and consequently to termination of the lasing process. The presence of the dopand molecules seems to strongly promote the formation and stabilization of the species which we relate to triplet excitons. Therefore, the concentration of the dopand affects the feasibility of quasi-cw operation of thin-film organic lasers. Strategies and results to achieve highly repetitive operation in low-threshold guest-host systems BN-PFO:DPAVB or BN-PFO:poly[2-methoxy-5-(2'-ethylhexyloxy)-1

  1. Amino resins crosslinked polymer gels for permeability profile control

    SciTech Connect

    Shu, P.

    1989-05-30

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

  2. Preliminary study of application of Moringa oleifera resin as polymer electrolyte in DSSC solar cells

    NASA Astrophysics Data System (ADS)

    Saehana, Sahrul; Darsikin, Muslimin

    2016-04-01

    This study reports the preliminary study of application of Moringa oleifera resin as polymer electrolyte in dye-sensitized solar cell (DSSC). We found that polymer electrolyte membrane was formed by using solution casting methods. It is observed that polymer electrolyte was in elastic form and it is very potential to application as DSSC component. Performance of DSSC which employing Moringa oleifera resin was also observed and photovoltaic effect was found.

  3. Evaluation of Resin Dissolution Using an Advanced Oxidation Process - 13241

    SciTech Connect

    Goulart de Araujo, Leandro; Vicente de Padua Ferreira, Rafael; Takehiro Marumo, Julio; Passos Piveli, Roque; Campos, Fabio

    2013-07-01

    The ion-exchange resin is widely used in nuclear reactors, in cooling water purification and removing radioactive elements. Because of the long periods of time inside the reactor system, the resin becomes radioactive. When the useful life of them is over, its re-utilization becomes inappropriate, and for this reason, the resin is considered radioactive waste. The most common method of treatment is the immobilization of spent ion exchange resin in cement in order to form a solid monolithic matrix, which reduces the radionuclides release into the environment. However, the characteristic of contraction and expansion of the resin limits its incorporation in 10%, resulting in high cost in its direct immobilization. Therefore, it is recommended the utilization of a pre-treatment, capable of reducing the volume and degrading the resin, which would increase the load capacity in the immobilization. This work aims to develop a method of degradation of ion spent resins from the nuclear research reactor of Nuclear and Energy Research Institute (IPEN/CNEN-SP), Brazil, using the Advanced Oxidative Process (AOP) with Fenton's reagent (hydrogen peroxide and ferrous sulphate as catalyst). The resin evaluated was a mixture of cationic (IR 120P) and anionic (IRA 410) resins. The reactions were conducted by varying the concentration of the catalyst (25, 50, 100 e 150 mM) and the volume of the hydrogen peroxide, at three different temperatures, 50, 60 and 70 deg. C. The time of reaction was three hours. Total organic carbon content was determined periodically in order to evaluate the degradation as a function of time. The concentration of 50 mM of catalyst was the most effective in degrading approximately 99%, using up to 330 mL of hydrogen peroxide. The most effective temperature was about 60 deg. C, because of the decomposition of hydrogen peroxide in higher temperatures. TOC content was influenced by the concentration of the catalyst, interfering in the beginning of the degradation

  4. Boswellia gum resin/chitosan polymer composites: Controlled delivery vehicles for aceclofenac.

    PubMed

    Jana, Sougata; Laha, Bibek; Maiti, Sabyasachi

    2015-01-01

    This study was undertaken to evaluate the effect of Boswellia gum resin on the properties of glutaraldehyde (GA) crosslinked chitosan polymer composites and their potential as oral delivery vehicles for a non-steroidal anti-inflammatory drug, aceclofenac. The incorporation of resinous material caused a significant improvement in drug entrapment efficiency (∼40%) of the polymer composites. Fourier transform infrared (FTIR) spectroscopic analysis confirmed the formation of chitosan-gum resin composites and did not show any evidence of drug-polymer chemical interaction. Field emission scanning electron microscopy (FE-SEM) suggested the formation of particulate polymer composites up to chitosan:gum resin mass ratio of 1:3. Only 8-17% drug was released into HCl solution (pH 1.2) in 2h. The drug release rate of polymer composites was faster in phosphate buffer solution (pH 6.8). The composites released ∼60-68% drug load in 7h. In same duration, the drug release rate suddenly boosted up to 92% as the concentration of gum resin in the composites was raised to 80%. The drug release mechanism deviated from non-Fickian to case-II type with increasing resin concentration in the composites. Hence, GA-treated Boswellia resin-chitosan composites could be considered as alternative vehicles for oral delivery of aceclofenac. PMID:25825076

  5. Dielectric relaxations investigation of a synthesized epoxy resin polymer

    NASA Astrophysics Data System (ADS)

    Jilani, Wissal; Mzabi, Nissaf; Gallot-Lavallée, Olivier; Fourati, Najla; Zerrouki, Chouki; Zerrouki, Rachida; Guermazi, Hajer

    2015-04-01

    A diglycidylether of bisphenol A (DGEBA) epoxy resin was synthesized, and cured with 3,3'-diaminodiphenyl sulfone (DDS) at a curing temperature of 120 °C. The relaxation properties of the realized polymers were studied by two complementary techniques: dielectric relaxation spectroscopy (DRS), in the temperature range 173-393K and in the frequency interval 10-1-106 Hz, and thermally stimulated depolarization current (TSDC) with a windowing polarization process. Current-voltage (I-V) measurements were also carried out to study interfacial relaxations. Dielectric data were analyzed in terms of permittivity and electric modulus variations. Three relaxation processes ( γ, β and α) have been identified. They were found to be frequency and temperature dependent and were interpreted in terms of the Havriliak-Negami approach. Relaxation parameters were determined by fitting the experimental data. The temperature dependence of the relaxation time was well fitted by the Arrhenius law for secondary relaxations, while the Vogel-Fulcher-Tamann model was found to better fit the τ( T) variations for α relaxation. We found τ 0 = 4.9 10-12 s, 9.6 10-13 s and 1.98 10-7 s for γ, β and α relaxations, respectively. The obtained results were found to be consistent with those reported in the literature. Due to the calculation of the low-frequency data of dielectric loss by the Hamon approximation, the Maxwell-Wagner-Sillars (MWS) relaxation was highlighted.

  6. Sustainable UV-curable low refractive index resins with novel polymers for polymer cladding materials

    NASA Astrophysics Data System (ADS)

    Tokoro, Hiroki; Ishikawa, Takako; Koike, Nobuyuki; Yamashina, Yohzoh

    2014-03-01

    Low refractive index polymers are used as cladding materials for high numerical aperture (NA) fibers. Since transparent fluoro polymers are ideal for this application, they have been used over many years. However, some fluoro chemicals face an issue related to perfluoro octanoic acid (PFOA) which is caused by its longtime persistence in the environment and human body. In this research, non-PFOA type UV curable fluoro resins suitable for cladding were developed with novel materials. The cured films showed high transparency, good adhesion to glass and low refractive index of 1.359 and 1.386 at 850 nm. Optical fibers prepared with those cladding showed almost equivalent attenuation to a fiber with commercially available material.

  7. Engineered Polymers for Advanced Drug Delivery

    PubMed Central

    Kim, Sungwon; Kim, Jong-Ho; Jeon, Oju; Kwon, Ick Chan; Park, Kinam

    2009-01-01

    Engineered polymers have been utilized for developing advanced drug delivery systems. The development of such polymers has caused advances in polymer chemistry, which, in turn, has resulted in smart polymers that can respond to changes in environmental condition, such as temperature, pH, and biomolecules. The responses vary widely from swelling/deswelling to degradation. Drug-polymer conjugates and drug-containing nano/micro-particles have been used for drug targeting. Engineered polymers and polymeric systems have also been used in new areas, such as molecular imaging as well as in nanotechnology. This review examines the engineered polymers that have been used as traditional drug delivery and as more recent applications in nanotechnology. PMID:18977434

  8. 77 FR 16508 - National Emission Standards for Hazardous Air Pollutant Emissions: Group IV Polymers and Resins...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-21

    ..., was published on January 9, 2012 (77 FR 1268). EPA has established the public docket for the proposed...: Group IV Polymers and Resins; Pesticide Active Ingredient Production; and Polyether Polyols Production... pollutants: National Emission Standards for Hazardous Air Pollutant Emissions: Group IV Polymers and...

  9. Therapeutic polymers for dental adhesives: Loading resins with bio-active components

    PubMed Central

    Imazato, Satoshi; Ma, Sai; Chen, Ji-hua; Xu, Hockin H.K.

    2014-01-01

    Objectives Many recent adhesives on the market exhibit reasonable clinical performance. Future innovations in adhesive materials should therefore seek out novel properties rather than simply modifying existing technologies. It is proposed that adhesive materials that are “bio-active” could contribute to better prognosis of restorative treatments. Methods This review examines the recent approaches used to achieve therapeutic polymers for dental adhesives by incorporating bio-active components. A strategy to maintain adhesive restorations is the focus of this paper. Results Major trials on therapeutic dental adhesives have looked at adding antibacterial activities or remineralization effects. Applications of antibacterial resin monomers based on quaternary ammonium compounds have received much research attention, and the loading of nano-sized bioactive particles or multiple ion-releasing glass fillers have been perceived as advantageous since they are not expected to influence the mechanical properties of the carrier polymer. Significance The therapeutic polymer approaches described here have the potential to provide clinical benefits. However, not many technological applications in this category have been successfully commercialized. Clinical evidence as well as further advancement of these technologies can be a driving force to make these new types of materials clinically available. PMID:23899387

  10. Development of new and improved polymer matrix resin systems, phase 1

    NASA Technical Reports Server (NTRS)

    Hsu, M. S.

    1983-01-01

    Vinystilbazole (vinylstryrylpyridine) and vinylpolystyrulpyridine were prepared for the purpose of modifying bismaleimide composite resins. Cure studies of resins systems were investigated by differential scanning calorimetry. The vinylstyrylpyridine-modified bismaleimide composite resins were found to have lower cure and gel temperatures, and shorter cure times than the corresponding unmodified composite resins. The resin systems were reinforced with commercially avialable satin-weave carbon cloth. Prepregs were fabricated by solvent or hot melt techniques. Thermal stability, flammability, moisture absorption, and mechanical properties of the composites (such as flexural strength, modulus, tensile and short beam shear strength) were determined. Composite laminates showed substantial improvements in both processability and mechanical properties compared to he bismaleimide control systems. The vinylstyrylpyridine modified bismaleimide resins can be used as advanced matrix resins for graphite secondary structures where ease of processing, fireworthiness, and high temperature stability are required for aerospace applications.

  11. Advanced resin systems and 3D textile preforms for low cost composite structures

    NASA Technical Reports Server (NTRS)

    Shukla, J. G.; Bayha, T. D.

    1993-01-01

    Advanced resin systems and 3D textile preforms are being evaluated at Lockheed Aeronautical Systems Company (LASC) under NASA's Advanced Composites Technology (ACT) Program. This work is aimed towards the development of low-cost, damage-tolerant composite fuselage structures. Resin systems for resin transfer molding and powder epoxy towpreg materials are being evaluated for processability, performance and cost. Three developmental epoxy resin systems for resin transfer molding (RTM) and three resin systems for powder towpregging are being investigated. Various 3D textile preform architectures using advanced weaving and braiding processes are also being evaluated. Trials are being conducted with powdered towpreg, in 2D weaving and 3D braiding processes for their textile processability and their potential for fabrication in 'net shape' fuselage structures. The progress in advanced resin screening and textile preform development is reviewed here.

  12. Boron/aluminum graphite/resin advanced fiber composite hybrids

    NASA Technical Reports Server (NTRS)

    Chamis, C. C.; Lark, R. F.; Sullivan, T. L.

    1975-01-01

    Fabrication feasibility and potential of an adhesively bonded metal and resin matrix fiber-composite hybrid are determined as an advanced material for aerospace and other structural applications. The results show that using this hybrid concept makes possible a composite design which, when compared with nonhybrid composites, has greater transverse strength, transverse stiffness, and impact resistance with only a small penalty on density and longitudinal properties. The results also show that laminate theory is suitable for predicting the structural response of such hybrids. The sequence of fracture modes indicates that these types of hybrids can be readily designed to meet fail-safe requirements.

  13. Ladder polymers for use as high temperature stable resins or coatings

    NASA Technical Reports Server (NTRS)

    Meador, Mary Ann (Inventor)

    1990-01-01

    An object of the invention is to synthesize a new class of ladder and partial ladder polymers. In accordance with the invention, the new class of ladder and partial ladder polymers are synthesized by polymerizing a bis-dienophile with a bis-diene. Another object of the invention is to provide a fabricated, electrically conducting, void free composite comprising the new class of the ladder and partial ladder polymers described above. The novelty of the invention relates to a new class of ladder and partial ladder polymers and a process for synthesizing these polymers. These polymers are soluble in common organic solvents and are characterized with a unique dehydration property at temperatures of 300 to 400 C to provide thermo-oxidatively stable pentiptycene units along the polymeric backbone. These polymers are further characterized with high softening points and good thermo-oxidative stability properties. Thus these polymers have potential as processable, matrix resins for high temperature composite applications.

  14. Recent advances in photorefractive polymers

    NASA Astrophysics Data System (ADS)

    Thomas, Jayan; Christenson, C. W.; Lynn, B.; Blanche, P.-A.; Voorakaranam, R.; Norwood, R. A.; Yamamoto, M.; Peyghambarian, N.

    2011-10-01

    Photorefractive composites derived from conducting polymers offer the advantage of dynamically recording holograms without the need for processing of any kind. Thus, they are the material of choice for many cutting edge applications, such as updatable three-dimensional (3D) displays and 3D telepresence. Using photorefractive polymers, 3D images or holograms can be seen with the unassisted eye and are very similar to how humans see the actual environment surrounding them. Absence of a large-area and dynamically updatable holographic recording medium has prevented realization of the concept. The development of a novel nonlinear optical chromophore doped photoconductive polymer composite as the recording medium for a refreshable holographic display is discussed. Further improvements in the polymer composites could bring applications in telemedicine, advertising, updatable 3D maps and entertainment.

  15. Structural use of polymer concrete made with resins based on recycled PET

    SciTech Connect

    Rebeiz, K.S.; Fowler, D.W.

    1995-08-01

    Recycled poly(ethylene terephthalate), PET, plastic waste can be used to produce unsaturated polyester resins. The PET waste is typically found in used beverage bottles that are collected after use in many localities. This research investigated the use of suitable unsaturated polyester resins based on recycled PET for the production of polymer concrete (PC) materials. The properties and structural behavior of unreinforced and steel-reinforced PC materials using resins based on recycled PET were found to be comparable to those obtained with PC materials using virgin resins. Resins based on recycled PET can also relatively easily be altered to achieve a wide variety of properties and performances in the PC. An experimental design also showed that the effect of the level of PET in the resin did not adversely affect the neat resin and the PC mechanical properties. Resins based on recycled PET help in decreasing the cost of PC products, saving energy, and alleviating an environmental problem posed by plastics waste.

  16. The Effect of Surface Roughness on Repair Bond Strength of Light-Curing Composite Resin to Polymer Composite Substrate

    PubMed Central

    Kallio, Timo T.; Tezvergil-Mutluay, Arzu; Lassila, Lippo V.J.; Vallittu, Pekka K.

    2013-01-01

    Objective: The purpose of this study was to analyze the shear bond strength of a new composite resin to polymer-based composite substrates using various surface roughnesses and two kinds of polymer matrices. Materials and methods: Particulate filler composite resin with cross-linked polymer matrix and fiber-reinforced composite with semi-interpenetrating polymer matrix were used as bonding substrates after being ground to different roughnesses. Substrates were aged in water for one week before bonding to new resin composites. Twelve specimens in the substrate groups were ground with grinding papers of four grits; 320, 800, 1200 and 2400. Results: Corresponding values of surface roughness (Ra) varied from 0.09 to 0.40 for the particulate filler composite resin and 0.07 to 0.96 for the fiber-reinforced composite resin. Characteristic shear bond strength between the new resin and particulate filler composite resin was highest (27.8 MPa) with the roughest surface (Weibull modulus: 2.085). Fiber-reinforced composite showed the highest bond strength (20.8 MPa) with the smoothest surface (Weibull modulus: 4.713). Conclusions: We concluded that surface roughness did not increase the bonding of new resin to the substrate of IPN based fiber-reinforced composite, whereas the roughness contributed to bonding the new resin to the particulate filler composite resin with a cross-linked polymer matrix. PMID:24167536

  17. 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.

  18. Boron/aluminum-graphite/resin advanced fiber composite hybrids

    NASA Technical Reports Server (NTRS)

    Chamis, C. C.; Lark, R. F.; Sullivan, T. L.

    1974-01-01

    An investigation was conducted to determine the fabrication feasibility and to assess the potential of adhesively-bonded metal and resin matrix fiber composite hybrids as an advanced material, for aerospace and other structural applications. The results of fabrication studies and of evaluation of physical and mechanical properties show that using this hybrid concept it is possible to design a composite which, when compared to nonhybrid composites, has improved transverse strength, transverse stiffness, and impact resistance with only a small penalty on density and longitudinal properties. The results also show that laminate theory is suitable for perdicting the structural response of such hybrids. The sequence of fracture modes indicates that these types of hybrids can be readily designed to meet fail-safe requirements.

  19. Boron/aluminum-graphite/resin advanced fiber composite hybrids

    NASA Technical Reports Server (NTRS)

    Chamis, C. C.; Lark, R. F.; Sullivan, T. L.

    1974-01-01

    An investigation was conducted to determine the fabrication feasibility and to assess the potential of adhesively-bonded metal and resin matrix fiber composite hybrids as an advanced material, for aerospace and other structural applications. The results of fabrication studies and of evaluation of physical and mechanical properties show that using this hybrid concept it is possible to design a composite which, when compared to nonhybrid composites, has improved transverse strength, transverse stiffness, and impact resistance with only a small penalty on density and longitudinal properties. The results also show that laminate theory is suitable for predicting the structural response of such hybrids. The sequence of fracture modes indicates that these types of hybrids can be readily designed to meet fail-safe requirements.

  20. Redox polymer electrodes for advanced batteries

    DOEpatents

    Gregg, Brian A.; Taylor, A. Michael

    1998-01-01

    Advanced batteries having a long cycle lifetime are provided. More specifically, the present invention relates to electrodes made from redox polymer films and batteries in which either the positive electrode, the negative electrode, or both, comprise redox polymers. Suitable redox polymers for this purpose include pyridyl or polypyridyl complexes of transition metals like iron, ruthenium, osmium, chromium, tungsten and nickel; porphyrins (either free base or metallo derivatives); phthalocyanines (either free base or metallo derivatives); metal complexes of cyclams, such as tetraazacyclotetradecane; metal complexes of crown ethers and metallocenes such as ferrocene, cobaltocene and ruthenocene.

  1. Redox polymer electrodes for advanced batteries

    DOEpatents

    Gregg, B.A.; Taylor, A.M.

    1998-11-24

    Advanced batteries having a long cycle lifetime are provided. More specifically, the present invention relates to electrodes made from redox polymer films and batteries in which either the positive electrode, the negative electrode, or both, comprise redox polymers. Suitable redox polymers for this purpose include pyridyl or polypyridyl complexes of transition metals like iron, ruthenium, osmium, chromium, tungsten and nickel; porphyrins (either free base or metallo derivatives); phthalocyanines (either free base or metallo derivatives); metal complexes of cyclams, such as tetraazacyclotetradecane; metal complexes of crown ethers and metallocenes such as ferrocene, cobaltocene and ruthenocene. 2 figs.

  2. Recent Advances in Simulation of Dendritic Polymers

    SciTech Connect

    Cagin, Tahir; Miklis, Paul J.; Wang, Guofeng; Zamanakos, Georgios; Martin, Ryan; Li, Hao; Mainz, Daniel T.; Nagarajan, V.; Goddard, William A.

    1999-05-11

    Dendrimers and hyperbranched polymers represent a revolution in methodology for directed synthesis of monodisperse polymers with enormous possibility of novel architectures. They demonstrate the ability to attain micelle-like structures with distinct internal and external character. Furthermore, the polyfunctional character of dendrimers allows varied response to environment and promise as selective sensors, carrier for drugs, encapsulation of toxic chemicals and metals. One of the key problems is the characterization of the structures. Theory and simulation can be essential to provide and predict structure and properties. We present some recent advances in theory, modeling and simulation of dendritic polymers.

  3. 21 CFR 177.1650 - Polysulfide polymer-polyepoxy resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1650 Polysulfide polymer...(dimethylaminomethyl) phenol, to which have been added certain optional substances to impart desired...

  4. Recent Advances in the Improvement of Polymer Electret Films

    NASA Astrophysics Data System (ADS)

    Erhard, Dominik P.; Lovera, Deliani; von Salis-Soglio, Cosima; Giesa, Reiner; Altstädt, Volker; Schmidt, Hans-Werner

    Polymer electret materials are electrically charged dielectric polymers capable of quasi-permanently retaining their electric field. However, environmental influences such as temperature and humidity reduce their charge stability and restrict applications. Therefore it is of great importance to provide a broad pool of polymer electret materials and to enhance further the charge storage behavior. In this context we report on concepts, measures, and solutions to improve the electret performance of commodity and high performance thermoplastic polymers, which was carried out at the University of Bayreuth in recent years. It is demonstrated that the commodity polymer polypropylene can be manufactured into excellent electret films when certain trisamide additives are incorporated in very low concentrations. Polypropylene can be employed at temperatures up to its continuous service temperature of 70 ∘C. To achieve higher temperature windows we investigated the commodity blend system of poly(phenylene ether) (PPE) and polystyrene (PS). We demonstrate that especially PPE/PS blend films with a composition of 75/25 exhibit remarkably good charge storage retention during the isothermal surface decay (ITPD) tests at 120 ∘C. In addition, the commercially available high performance thermoplastic polyetherimide (PEI) resin containing special phosphorus(III) additives shows very good electret properties at elevated temperatures. These properties can be further enhanced by physical aging; resulting in a charge retention after 24 h at 120 ∘C as high as 95%. The same beneficial effect of physical aging can be used to advance PPE and PPE/PS blends. Polymer electret materials with such charge storage properties have the potential to be employed in microphones, sensor devices, and electret filters.

  5. Fouling of anion exchange resin by fluorescence analysis in advanced treatment of municipal wastewaters.

    PubMed

    Li, Haibo; Li, Aimin; Shuang, Chendong; Zhou, Qing; Li, Wentao

    2014-12-01

    The application of anion exchange resins (AERs) has been limited by the critical problem of resin fouling, which increases the volume of the desorption concentrate and decreases treatment efficiency. To date, resin fouling has not been well studied and is poorly understood compared to membrane fouling. To reflect the resin fouling level, a resin fouling index (RFI) was established in this work according to the decrease of DOC removal after regeneration of the resin for the advanced treatment of municipal wastewater. Comparing the linear fitting results between the RFI and the fluorescence intensity indicated that the resin fouling was related to the protein-like substances with fluorescence peak T in the region of excitation wavelength <250 nm and emission wavelength <380 nm. Using their fluorescent characteristics as a label, the protein-like substances causing the fouling were further identified as hydrophilic components with molecular weights greater than 6500 Da. PMID:25218660

  6. Advances in inherently conducting polymers

    SciTech Connect

    Aldissi, M.

    1987-09-01

    The discovery of polyacetylene as the prototype material led to extensive research on its synythesis and characterization. The techniques that emerged as the most important and promising ones are those that dealt with molecular orientation and that resulted in conductivities almost as high as that of copper. The study of dozens of other materials followed. Interest in conducting polymers stems from their nonclassical optical and electronic properties as well as their potential technological applications. However, some of the factors currently limiting their use are the lack of long-term stability and the need to develop conventional low-cost techniques for easy processing. Therefore, research was extended toward solving these problems, and progress has been recently made in that direction. The synthesis of new materials such as stable and easily processable alkylthiophenes, water-soluble polymers, and multicomponent systems, including copolymers and composites, constitutes an important step forward in the area of synthetic metals. However, a full understanding of materials chemistry and properties requires more work in the years to come. Although, few small-scale applications have proven to be successful, long-term stability and applicability tests are needed before their commercial use becomes reality.

  7. Micromechanical characterization of nonlinear behavior of advanced polymer matrix composites

    NASA Technical Reports Server (NTRS)

    Gates, Thomas S.; Chen, J. L.; Sun, C. T.

    1994-01-01

    Due to the presence of curing stresses and oriented crystalline structures in the matrix of polymer matrix fiber composites, the in situ nonlinear properties of the matrix are expected to be rather different from those of the bulk resin. A plane stress micromechanical model was developed to retrieve the in situ elastic-plastic properties of Narmco 5260 and Amoco 8320 matrices from measured elastic-plastic properties of IM7/5260 and IM7/8320 advance composites. In the micromechanical model, the fiber was assumed to be orthotropically elastic and the matrix to be orthotropic in elastic and plastic properties. The results indicate that both in situ elastic and plastic properties of the matrices are orthotropic.

  8. Fundamental studies of the properties of photoresists based on resins containing polymer-bound photoacid generators

    NASA Astrophysics Data System (ADS)

    Lee, Cheng-Tsung; Jarnagin, Nathan D.; Wang, Mingxing; Gonsalves, Kenneth E.; Robert, Jeanette M.; Yueh, Wang; Henderson, Clifford L.

    2006-03-01

    Conventional chemically amplified photoresist formulations are complex mixtures that include a protected polymer resin and a small molecule photoacid generator (PAG). The limited compatibility of the PAG with resist resin and the mobility of the small molecule additive can lead to problems including PAG phase separation, non-uniform initial PAG and photoacid distribution, and acid migration during the post-exposure baking (PEB) processes. The incorporation of PAG units into the main chain of the polymer resin is one possible method to alleviate these problems. Recently, we have investigated methacrylate based resists which incorporate novel PAG functional groups into the polymer main chain. These materials have demonstrated good resolution performance for both 193 nm and EUV exposure for sub-100 nm patterning. However, limited information is available on the effect of binding the PAG to the polymer on PAG photoreactivity and photoacid diffusivity. In this work, the photoacid generation rate constant (commonly referred to as the Dill C parameter for the PAG) of both triflate polymer-bound PAG and blended PAG photoresists based on poly(γ-butyrolactone methacrylate -co-2-ethyl-2-adamantyl methacrylate ) resists were determined by a new technique utilizing both quantitative FTIR spectroscopy and kinetic model fitting. The results indicate that the polymer-bound PAG resist has a lower photoacid generation rate constant (C=0.0122) than the blend PAG one (C=0.2647). This large difference in Dill C parameters would indicate that the sensitivity of the polymer-bound PAG resist is substantially lower than that of the analogous blended sample which is consistent with contrast curve data for these two samples.

  9. Amino resin modified xanthan polymer gels for permeability profile control

    SciTech Connect

    Shu, P.

    1988-01-05

    A process for closing pores in a hydrocarbonaceous fluid bearing formation to obtain improved sweep efficiency during a water flood oil recovery operation wherein the process comprises injecting into the formation a gellable composition is described comprising: (a) water; (b) about 0.2 to about 5.0 wt. percent of a cross linkable polysaccharide biopolymer having at least one functional group selected from a member of the group consisting of an amine, an amide, a hydroxyl, or a thiol group; (c) about 0.02 to about 5.0 wt. percent of an aminoplast resin which reinforces the biopolymer; and (d) sufficient transitional metal ions to form a gel of a size and strength sufficient to close one or more permeable zones in the formation under substantially all pH conditions.

  10. Microwave heated resin injector for advanced composite production.

    PubMed

    Stanculovic, Sebastijan; Feher, Lambert

    2008-01-01

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

  11. Hygrothermal response of polymer composites based on modified sisal fibers and unsaturated polyester resin

    SciTech Connect

    Singh, B.; Gupta, M.

    1995-10-01

    Polymer composites made from surface modified sisal fibers and unsaturated polyester resin were exposed to different wet environments and their physico-mechanical properties were evaluated as a function of exposure time. It was found that all types of treatments improved the performance of composites. Silane treated fiber composites displayed superior strength retention property under humid environments, while zirconate treated fiber composites resulted fairly better in immersed water condition.

  12. Advanced Polymers Containing the Phenyltrifluoroethylidene Connecting Group

    NASA Technical Reports Server (NTRS)

    Alstron, William B.; Sivko, Gloria S.

    2006-01-01

    A new, lower cost fluorinated dianhydride based on the phenyltrifluoroethylidene (3F) connecting linkage was invented by the principal author in the early 1980's. New 3F condensation and addition cured polyimides were synthesized with the newly discovered 3F dianhydride and the previously known 3F diamine. As controls, polyimides based on the somewhat analogous higher cost hexafluoroisopropylidene (6F) linkage were also prepared. The short term thermal oxidative stability (TOS), determined by thermal gravimetric analysis (TGA), and the glass transition temperatures (Tg) of 3F dianhydride polyimides were found to be similar to 6F dianhydride polyimides, but the Tg was slightly higher for 3F diamine polyimides than 6F diamine polyimides. Unfortunately, in real time testing, long term TOS of 3F polymers was clearly inferior to 6F polymers. This was due to a 3 to 5 fold greater rate of loss of trifluoromethyl group from 3F versus 6F linkages. However, at shorter times or lower temperatures, 3F TOS was almost comparable to 6F TOS. The wide scope of the 3F technology was also demonstrated to have distinct unique advantages over 6F technology through the use of the 3F pendant phenyl ring as a synthetic site to introduce other functional groups. These groups have been used for the control or modification of polymer properties; an advantage lacking within 6F technology. The synthetic ease by which 3F can be introduced into various types of monomers has lead to the explosion of advanced 3F polyimides and other high performance advanced 3F polymers in the prior decade of 3F polymer literature as cited herein; covering polyimides, substituted polyimides, at least ten types of nonpolyimide 3F polymer modifications, and also the government's nine 3F U.S. patents and corporations' nine 3F U.S. patents.

  13. Effect of resin type on the signal integrity of an embedded perfluorinated polymer optical fiber

    NASA Astrophysics Data System (ADS)

    Hamouda, Tamer; Peters, Kara; Seyam, Abdel-Fattah M.

    2012-05-01

    Polymer optical fibers (POF) hold many advantages for embedded sensing, such as their low cost, flexibility, high tensile strain limits and high fracture toughness. POF sensors may therefore be integrated into fiber reinforced composite structures for monitoring structural behavior. Since POFs do not require a protective coating, it is critical to verify that the resin system does not have a negative impact on the noise level or performance of POF sensors during composite manufacture. This study measured the effect of vinylester and epoxy resin systems on the signal loss of embedded perfluorinated, graded index POFs. Photon-counting optical time domain reflectometry (OTDR) was used to monitor the signal attenuation and backscattering level of the POFs throughout the resin curing cycle. Fourier transform infrared spectrometry (FTIR) and cross section analyses using scanning electronic microscope (SEM) images were also conducted to investigate whether the resin system caused chemical and physical changes of the POF. This study showed that vinylester resin caused a significant increase in the backscattering level of POF sensors and therefore induced high fiber signal losses. On the other hand, the POF treated with epoxy showed no change in backscattering level, indicating that no chemical or physical change had occurred to the POF.

  14. Differential scanning calorimetry investigation on vinyl ester resin curing process for polymer nanocomposite fabrication.

    PubMed

    Guo, Zhanhu; Ng, Ho Wai; Yee, Gary L; Hahn, H Thomas

    2009-05-01

    Two different ceramic (cerium oxide and titanium oxide) nanoparticles were introduced into vinyl ester resin for nanocomposite fabrication. The curing process of the vinyl ester resin was investigated by a differential scanning calorimetery (DSC). The incorporation of nanoparticles in the resin affects the curing process due to the physicochemical interaction between the nanoparticles and the polymer matrix. The particle loading has a significant effect on the initial and peak curing temperatures, reaction heat and curing extent. The fully cured vinyl ester resin nanocomposites reinforced with cerium oxide nanoparticles were fabricated after a 24-hour room temperature curing and a one-hour postcuring at 85 degrees C. Particle functionalization favors the composite fabrication with a higher curing extent after room-temperature curing as compared to the as-received nanoparticle filled vinyl ester resin nanocomposites. The nanofiller materials were observed to significantly affect the curing process. In comparison to cerium oxide nanoparticles, titanium oxide nanoparticles prohibit the curing process with a much higher initiating curing temperatures. The fully cured nanocomposites reinforced with titanium oxide nanoparticles were fabricated by one-hour postcuring at 85 degrees C. PMID:19453004

  15. Fast identification of selective resins for removal of genotoxic aminopyridine impurities via screening of molecularly imprinted polymer libraries.

    PubMed

    Kecili, Rustem; Billing, Johan; Nivhede, David; Sellergren, Börje; Rees, Anthony; Yilmaz, Ecevit

    2014-04-25

    This study describes the identification and evaluation of molecularly imprinted polymers (MIPs) for the selective removal of potentially genotoxic aminopyridine impurities from pharmaceuticals. Screening experiments were performed using existing MIP resin libraries to identify resins selective towards those impurities in the presence of model pharmaceutical compounds. A hit resin with a considerable imprinting effect was found in the screening and upon further investigation, the resin was found to show a broad selectivity towards five different aminopyridines in the presence of the two model active pharmaceutical ingredients (APIs) piroxicam and tenoxicam. PMID:24661866

  16. 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.

  17. Curing and toughening of epoxy resins with phosphorus containing monomers and polymers

    SciTech Connect

    Park, Y.R.; Park, I.Y.; Yoon, T.H.

    1996-12-31

    Epoxy resins have been utilized in many areas, from house holds to airplanes, for the past several decades due to some exceptional properties such as low cost, good mechanical properties and excellent adhesive properties. However, low fracture toughness and flame resistance of epoxy resins have limited their applicability. Therefore, enhancing those properties have been of great interest to many researchers and scientists. As introduced by McGrath and co-workers in 1980s, the reactive thermoplastic polymers have proven to be an excellent toughener for improving not only fracture toughness but also adhesive properties without sacrificing thermo-mechanical properties and chemical resistance. Flame retardency could be improved by adding flame retardent additives which are divided into two groups; additives and reactives. However, among the additives, halogen compounds are known to be toxic gas generator and ozone depleter. Moreover, additives could be potentially leached out of the material, while reactives are inferior to additives. Recently, a reactive type phosphine oxide containing flame retardants have been introduced by McGrath and co-workers and proven to be an excellent flame retardant. In this paper, phospine oxide containing monomers were prepared and utilized as curing agents for expoxy resins, and starting materials for the polymers.

  18. Thermosetting polymer for dynamic nuclear polarization: Solidification of an epoxy resin mixture including TEMPO

    NASA Astrophysics Data System (ADS)

    Noda, Yohei; Kumada, Takayuki; Yamaguchi, Daisuke; Shamoto, Shin-ichi

    2015-03-01

    We investigated the dynamic nuclear polarization (DNP) of typical thermosetting polymers (two-component type epoxy resins; Araldite® Standard or Araldite® Rapid) doped with a (2,2,6,6-tetramethylpiperidine-1-yl)oxy (TEMPO) radical. The doping process was developed by carefully considering the decomposition of TEMPO during the solidification of the epoxy resin. The TEMPO electron spin in each two-component paste decayed slowly, which was favorable for our study. Furthermore, despite the dissolved TEMPO, the mixture of the two-component paste successfully solidified. With the resulting TEMPO-doped epoxy-resin samples, DNP experiments at 1.2 K and 3.35 T indicated a magnitude of a proton-spin polarization up to 39%. This polarization is similar to that (35%) obtained for TEMPO-doped polystyrene (PS), which is often used as a standard sample for DNP. To combine this solidification of TEMPO-including mixture with a resin-casting technique enables a creation of polymeric target materials with a precise and complex structure.

  19. In-situ sensor monitoring of resin film infusion of advanced fiber architecture preforms

    SciTech Connect

    Kranbuehl, D.E.; Hood, D.; Rogozinski, J.

    1995-12-01

    Resin transfer molding (RTM) of advanced fiber architecture stitched preforms is being developed as a smart cost-effective manufacturing technique for fabricating damage tolerant composite structures with geometrically complex reinforcements. Dry textile preforms are infiltrated with resin and cured in a single step process, thus eliminating separate prepreg manufacture and ply-by-ply lay-up. The number of parameters that must be controlled during infiltration and cure make trial-and-error methods of process cycle optimization extremely inefficient. In situ cure monitoring sensors and an analytical processing model are a superior alternative for the determination of optimum processing cycles, quality assurance, and automated process control. Resin transfer molding experiments have been conducted in a manufacturing plant with a reactive epoxy resin and carbon fabric preforms. Frequency dependent electromagnetic sensing (FDEMS) was used to monitor in situ resin position, viscosity and degree of cure in situ in the mold during the Resin Transfer Molding infiltration and cure process. A science based multi-dimensional model of Resin Transfer Molding (RTM) was used to predict the infiltration behavior, as well as viscosity and degree of cure as the resin flows and cures in the dry textile preform.

  20. Advanced composites: Environmental effects on selected resin matrix materials

    NASA Technical Reports Server (NTRS)

    Welhart, E. K.

    1976-01-01

    The effects that expected space flight environment has upon the mechanical properties of epoxy and polyimide matrix composites were analyzed. Environmental phenomena covered water immersion, high temperature aging, humidity, lightning strike, galvanic action, electromagnetic interference, thermal shock, rain and sand erosion, and thermal/vacuum outgassing. The technology state-of-the-art for graphite and boron reinforced epoxy and polyimide matrix materials is summarized to determine the relative merit of using composites in the space shuttle program. Resin matrix composites generally are affected to some degree by natural environmental phenomena with polyimide resin matrix materials less affected than epoxies.

  1. The nature and fate of natural resins in the geosphere - VIII - NMR and Py-GC-MS characterization of soluble labdanoid polymers isolated from holocene class I resins.

    SciTech Connect

    Clifford, D. J.; Hatcher, P. G.; Botto, R. E.; Muntean, J. V.; Michaels, B.; Anderson, K. B.; Chemistry; Pennsylvania State Univ.; Amoco Oil Co.

    1997-01-01

    Soluble polylabdanoids isolated by sequential solvent extraction have been characterized by liquid-state {sup 13}C- and {sup 1}H NMR and {sup 13}C-{sup 1}H HMQC (heteronuclear correlation) NMR spectroscopy in addition to solid-state NMR and Py-GC-MS techniques. Two Holocene resins originating from Santander, Colombia and Mombasa, Kenya were analyzed. Soluble polymers were isolated by extraction with a 1:1 (v/v) methylene chloride-methanol mixture following sequential extractions with methylene chloride and methanol. The molecular weight of polymer extracts was shown by GPC analyses to exceed that of non-polymeric occluded terpenoids. Py-GC-MS, solid-state {sup 13}C CP/MAS and {sup 13}C cross-polarization/depolarization NMR spectroscopy results indicated that chemical compositions of soluble polymers isolated from immature resins are highly representative of the structure of corresponding insoluble polymers, i.e. polylabdatrienes. These data provide evidence for cross-linking or cyclization of side-chain olefinic carbons during or shortly after polymerization. Generally, the characterization of soluble resin polymers by liquid-state NMR spectroscopy has proven to be an excellent means for investigating the maturation mechanism of polylabdanoid resinites, and has potential for furthering the application of Class I resinites as geothermal indicators.

  2. Investigation of Polymer Resin/Fiber Compatibility in Natural Fiber Reinforced Composite Automotive Materials

    SciTech Connect

    Fifield, Leonard S.; Huang, Cheng; Simmons, Kevin L.

    2010-01-01

    Natural fibers represent a lower density and potentially lower cost alternative to glass fibers for reinforcement of polymers in automotive composites. The high specific modulus and strength of bast fibers make them an attractive option to replace glass not only in non-structural automotive components, but also in semi-structural and structural components. Significant barriers to insertion of bast fibers in the fiber reinforced automotive composite market include the high moisture uptake of this lignocellulosic material relative to glass and the weak inherent interface between natural fibers and automotive resins. This work seeks to improve the moisture uptake and resin interfacing properties of natural fibers through improved fundamental understanding of fiber physiochemical architecture and development of tailored fiber surface modification strategies.

  3. Resin transfer molding for advanced composite primary wing and fuselage structures

    NASA Technical Reports Server (NTRS)

    Markus, Alan

    1992-01-01

    The stitching and resin transfer molding (RTM) processes developed at Douglas Aircraft Co. are successfully demonstrating significant cost reductions with good damage tolerance properties. These attributes were identified as critical to application of advanced composite materials to commercial aircraft primary structures. The RTM/stitching developments, cost analyses, and test results are discussed of the NASA Advanced Composites Technology program.

  4. Resin transfer molding for advanced composite primary aircraft structures

    NASA Technical Reports Server (NTRS)

    Markus, Alan; Palmer, Ray

    1991-01-01

    Resin Transfer Molding (RTM) has been identified by Douglas Aircraft Company (DAC) and industry to be one of the promising processes being developed today which can break the cost barrier of implementing composite primary structures into a commercial aircraft production environment. The RTM process developments and scale-up plans Douglas Aircrart will be conducting under the NASA ACT contract are discussed.

  5. Formulation Study on Immobilization of Spent Ion Exchange Resins in Polymer Cements

    SciTech Connect

    Lili Xia; Meiqiong Lin; Bao Liangjin

    2006-07-01

    Applying normal design and correlative computer software, a new matrix material and an excellent waste formulation were developed. Based on the theory calculations and normal design in this paper, using polymer complex cement as immobilization matrix that mixed with simulating spent ion exchange resin a new waste formulation was carried out. The characterization of solidified waste had been done after 28 days curing. The results conformed to the treatment of the waste about the requests of the national standard [GB14569-93-1]. Leach index of the solidified waste was excellent. An optimized formulation was recommended. (authors)

  6. Thermal and Mechanical Characteristics of Polymer Composites Based on Epoxy Resin, Aluminium Nanopowders and Boric Acid

    NASA Astrophysics Data System (ADS)

    Nazarenko, O. B.; Melnikova, T. V.; Visakh, P. M.

    2016-01-01

    The epoxy polymers are characterized by low thermal stability and high flammability. Nanoparticles are considered to be effective fillers of polymer composites for improving their thermal and functional properties. In this work, the epoxy composites were prepared using epoxy resin ED-20, polyethylene polyamine as a hardener, aluminum nanopowder and boric acid fine powder as flame-retardant filler. The thermal characteristics of the obtained samples were studied using thermogravimetric analysis and differential scanning calorimetry. The mechanical characteristics of epoxy composites were also studied. It was found that an addition of all fillers enhances the thermal stability and mechanical characteristics of the epoxy composites. The best thermal stability showed the epoxy composite filled with boric acid. The highest flexural properties showed the epoxy composite based on the combination of boric acid and aluminum nanopowder.

  7. The enhancing effect of mesogen-jacketed liquid crystalline polymer PBPCS on epoxy resin

    NASA Astrophysics Data System (ADS)

    Chai, C. P.; Li, X. J.; Zhu, Y.; Gao, Y. X.; Li, G. P.; Luo, Y. J.

    2015-12-01

    The mixtures of mesogen-jacketed liquid crystalline polymers (MJLCP) and epoxy resin (E-51) have been prepared in a certain proportion. The category of the MJLCP is poly{2, 5-bis[(4-butoxyphenyl) oxycarbonyl] styrenes} (PBPCS). Methyl tetrahydro phthalic anhydride (MeTHPA) is served as a curing agent, and N, N-dimethylbenzylamine plays the role of catalyst. Then, based on the curing process, the modified materials have been acquired by casting molding. The effect of PBPCS's improvement has been researched through the mechanical properties test, dynamic thermal mechanical test and scanning electron microscope (SEM). The results indicated that PBPCS could apparently improve the mechanical properties of resin E-51. Compared with unmodified materials, the elongation at break and the tensile strength of PBPCS have been improved remarkably through modification. Both mechanical properties of the 4wt% PBPCS/E-51/MeTHPA were enhanced by 48% and 153% separately, and the characteristics of the 3wt% one were raised by 47% and 19% respectively. Also, the ductile fracture morphology of the resins was exhibited in SEM photograph clearly.

  8. Evaluation of bisphenol E cyanate ester for the resin-injection repair of advanced composites

    NASA Astrophysics Data System (ADS)

    Lio, Wilber Yaote

    Polymer matrix composites (PMCs) are susceptible to impacts that often result in microcracks and delaminations that can greatly reduce their mechanical integrity. Current injection repair techniques are limited to low glass transition temperature (Tg) composites due to the temperature and viscosity limitations of current repair resins. Bisphenol E cyanate ester (BECy) has both a high Tg and low prepolymer viscosity that makes it an ideal resin for the injection repair of high temperature PMCs. In addition, alumina nanoparticles have been shown to increase the strengths of some adhesives as well as impart shear thinning properties in suspension; both of which are desirable effects for injection repair. Lap shear tests were performed to evaluate adhesive properties of BECy and BECy-alumina nanocomposites. Effects of substrate, temperature, nanoparticle loading, and moisture were investigated. A resin-injection process was developed and the efficiency of BECy in repairing bismaleimide-carbon fiber composite plates was studied through ultrasonic evaluation and compression-after-impact tests.

  9. Mechanical characterization and structural analysis of recycled fiber-reinforced-polymer resin-transfer-molded beams

    NASA Astrophysics Data System (ADS)

    Tan, Eugene Wie Loon

    1999-09-01

    The present investigation was focussed on the mechanical characterization and structural analysis of resin-transfer-molded beams containing recycled fiber-reinforced polymers. The beams were structurally reinforced with continuous unidirectional glass fibers. The reinforcing filler materials consisted entirely of recycled fiber-reinforced polymer wastes (trim and overspray). The principal resin was a 100-percent dicyclo-pentadiene unsaturated polyester specially formulated with very low viscosity for resin transfer molding. Variations of the resin transfer molding technique were employed to produce specimens for material characterization. The basic materials that constituted the structural beams, continuous-glass-fiber-reinforced, recycled-trim-filled and recycled-overspray-filled unsaturated polyesters, were fully characterized in axial and transverse compression and tension, and inplane and interlaminar shear, to ascertain their strengths, ultimate strains, elastic moduli and Poisson's ratios. Experimentally determined mechanical properties of the recycled-trim-filled and recycled-overspray-filled materials from the present investigation were superior to those of unsaturated polyester polymer concretes and Portland cement concretes. Mechanical testing and finite element analyses of flexure (1 x 1 x 20 in) and beam (2 x 4 x 40 in) specimens were conducted. These structurally-reinforced specimens were tested and analyzed in four-point, third-point flexure to determine their ultimate loads, maximum fiber stresses and mid-span deflections. The experimentally determined load capacities of these specimens were compared to those of equivalent steel-reinforced Portland cement concrete beams computed using reinforced concrete theory. Mechanics of materials beam theory was utilized to predict the ultimate loads and mid-span deflections of the flexure and beam specimens. However, these predictions proved to be severely inadequate. Finite element (fracture propagation

  10. Novel injectable and in situ curable glycolide/lactide based biodegradable polymer resins and composites.

    PubMed

    Xie, Dong; Park, Jong-Gu; Zhao, Jun; Turner, Charles H

    2007-07-01

    Novel in situ polymerizable liquid three-arm biodegradable oligomeric polyesters based upon glycolic acid (GA), L-lactic acid (LLA), and their copolymers are synthesized and characterized. Injectable and in situ curable polymer neat resins and their composites formulated with bioabsorbable beta-tricalcium phosphate are prepared at room temperature using photo- and redox-initiation systems, respectively. The cured neat resins show the initial compressive yield strength (YCS, MPa), modulus (M, MPa), ultimate compressive strength (UCS, MPa), and toughness (T, kN mm), ranging from 4.0 to 20.1, 201.5 to 730.2, 82.7 to 310.5, and 1.02 to 3.93. The cured composites show the initial YCS, M, UCS and T, ranging from 27.7 to 56.4, 1440 to 4870, 81.6 to 158.9, and 0.94 to 1.97. Increasing GA/LLA ratio increases all the initial compressive strengths of both neat resins and composites. Increasing filler content increases YCS and M but decreases UCS and T. A diametral tensile strength test shows the same trend as a compressive strength test. There seems to be an optimal flexural strength for the composite at the filler content around 43%. An increasing molar ratio increases curing time but decreases the degree of conversion (DC). An increasing filler content increases curing time but decreases exotherm and DC. During the course of degradation, all the materials show a burst degradation behavior within 24 h, followed by an increase in CS. The poly(glycolic acid) neat resin completely loses its strength at around Day 45. The composites completely lose their strengths at different time intervals, depending on their molar ratio and filler content. The degradation rate is found to be molar ratio and filler-content dependent. PMID:16920760

  11. Advances in shape-memory polymer actuation

    NASA Astrophysics Data System (ADS)

    Leng, Jinsong; Liu, Yanju; Lan, Xin

    2009-03-01

    Shape memory polymer (SMP) is a promising smart material, which is able to perform a large deformation upon applying an external stimulus, such as heat, light and moisture, etc. In recent years, many investigations have been advanced in thermo-responsive SMP actuation, and several novel actuations have been applied in SMP. In this paper, the mechanism and demonstration of three types of SMP actuations (infrared laser, physical swelling effect and electricity) are presented. These novel actuation approaches may help SMP to fully reach its potential application. Firstly, for the infrared laser-activated SMP, it is concerned about the drive of SMP by infrared light. The infrared laser, transmitted through the optical fiber embedded in the SMP matrix, was chosen to drive the SMP. The working frequency of infrared laser was installed in 3-4μm. Moreover, this paper presents a study on the effects of solution on the glass transition temperature (Tg). It shows that the hydrogen bonding of SMP was aroused by the absorbed solution that significantly reduces transition temperature of polymer. In this way, the shape memory effect (SME) can undergo solution-driven shape recovery. Finally, the actuation of two types of electro-active SMP composites filled with electrically conductive powders (carbon black, nickel powers) have been carried out, and the SMP composite can be driven by applying a relatively low voltage.

  12. Evaluation of bisphenol E cyanate ester for the resin-injection repair of advanced composites

    SciTech Connect

    Lio, Wilber Yaote

    2009-12-01

    This thesis is a compilation of a general introduction and literature review that ties together the subsequent chapters which consist of two journal articles that have yet to be submitted for publication. The overall topic relates to the evaluation and application of a new class of cyanate ester resin with unique properties that lend it applicable to use as a resin for injection repair of high glass transition temperature polymer matrix composites. The first article (Chapter 2) details the evaluation and optimization of adhesive properties of this cyanate ester and alumina nanocomposites under different conditions. The second article (Chapter 3) describes the development and evaluation of an injection repair system for repairing delaminations in polymer matrix composites.

  13. Recent advances in the chemistry and applications of the Diphonix resins

    SciTech Connect

    Horwitz, E.P.; Chiarizia, R.; Alexandratos, S.D.; Gula, M.

    1997-10-01

    The Diphonix class of ion exchange resins is characterized by the presence of geminally substituted diphosphonic acid groups chemically bonded to a polymer matrix. Regular Diphonix contains gem-diphosphonic groups chemically bonded to a sulfonated styrene-divinylbenzene matrix. Modification of the properties of Regular Diphonix are achieved by the introduction of additional functional groups such as anion exchange groups in Diphonix-A and phenolic groups in Diphonix-CS. Diphosil has a silica matrix in which the gem-diphosphonic groups are chemically bonded to an organic polymer graft that surrounds the silica particles. Applications of the Diphonix resins range from treatment of a variety of radioactive waste to iron control in hydrometallurgy and semiconductor manufacture.

  14. Effects of Molecular Structure in Macroscopic Mechanical Properties of an Advanced Polymer (LARC(sup TM)-SI)

    NASA Technical Reports Server (NTRS)

    Nicholson, Lee M.; Hinkley, Jeffrey A.; Whitley, Karen S.; Gates, Thomas S.

    2004-01-01

    Mechanical testing of an advanced polymer resin with known variations in molecular weight was performed over a range of temperatures below the glass transition temperature. The elastic properties, inelastic elongation behavior, and notched tensile strength all as a function of molecular weight and test temperature were determined. It was shown that notched tensile strength is a strong function of both temperature and molecular weight, whereas stiffness is only a strong function of temperature.

  15. Polymers as advanced materials for desiccant applications

    SciTech Connect

    Czanderna, A.W.

    1990-12-01

    This research is concerned with solid materials used as desiccants for desiccant cooling systems (DCSs) that process water vapor in an atmosphere to produce cooling. Background information includes an introduction to DCSs and the role of the desiccant as a system component. The water vapor sorption performance criteria used for screening the modified polymers prepared include the water sorption capacity from 5% to 80% relative humidity (R.H.), isotherm shape, and rate of adsorption and desorption. Measurements are presented for the sorption performance of modified polymeric advanced desiccant materials with the quartz crystal microbalance. Isotherms of polystyrene sulfonic acid (PSSA) taken over a 5-month period show that the material has a dramatic loss in capacity and that the isotherm shape is time dependent. The adsorption and desorption kinetics for PSSA and all the ionic salts of it studied are easily fast enough for commercial DCS applications with a wheel rotation speed of 6 min per revolution. Future activities for the project are addressed, and a 5-year summary of the project is included as Appendix A. 34 refs., 20 figs., 3 tabs.

  16. Injection repair of advanced aircraft composites with a high temperature cyanate ester resin

    NASA Astrophysics Data System (ADS)

    Bauer, Amy Elizabeth

    Polymer matrix composites, especially those with carbon fiber reinforcement, are becoming increasingly common in aerospace applications due to their high stiffness to weight ratio, resulting in significant weight and fuel savings on commercial and military aircraft. Despite their excellent properties, carbon fiber composites are often susceptible to damage in the form of delaminations or interlaminar cracking caused by low energy impact or manufacturing defects. Often not easily detectable, delaminations are detrimental to the strength of the composite and can ultimately result in failure of the component. Therefore methods must be developed to repair damaged composites. Injection repair is a procedure that involves injecting a low viscosity resin into the damaged area and subjecting the composite to heat to cure the resin. Currently, injection repairs are rarely used in high temperature applications because of the lack of resins with both low viscosity and high thermal stability. Therefore demonstrating the use of a resin with satisfactory viscosity and Tg requirements would expand the application of injection repairs to more vigorous environments. In the present study, the injection repair method was developed to repair damaged bismaleimide carbon fiber composites that are similar to composites used on several high temperature weapon platforms. Bisphenol E cyanate ester (BECy) was chosen as the injection resin due to having the unique combination of low viscosity and a high glass transition temperature. Cure kinetic studies found an optimum undercure schedule to achieve the maximum T g while avoiding the high temperature postcure. Mechanical and adhesive tests revealed that partially cured BECy had properties superior to that of the fully cured resin. Following the evaluation of the resin, the injection repair procedure and set up were developed. Successful and reproducible repairs were performed on panels pre-damaged through static loading and drop tower impact

  17. Plasticization and crosslinking effects of acetone-formaldehyde and tannin resins on wheat protein-based natural polymers.

    PubMed

    Zhang, Xiaoqing; Do, My Dieu

    2009-07-01

    Efficient plasticization and sufficient crosslinking were achieved by using an acetone-formaldehyde (AF) resin as an additive in the thermal processing of wheat protein-based natural polymers. The mobile AF resin and its strong intermolecular interactions with a wheat protein matrix produced sufficient flexibility for the plastics, while the covalent bonds formed between AF and the protein chains also caused the water-soluble resin to be retained in the materials under wet conditions. The mechanical properties of the materials were also enhanced as an additional benefit due to the formation of crosslinked networks through the polymer matrix. Tensile strength was further enhanced when using AF in conjunction with tannin resin (AFTR) in the systems as rigid aromatic structures were formed in the crosslinking segments. Different components in wheat proteins (WPs) or wheat gluten (WG) (e.g., proteins, residual starch and lipids) displayed different capabilities in interaction and reaction with the AFTR additives, and thus resulted in different performances when the ratio of these components varied in the materials. The application of the AFTR additives provides a feasible methodology to thermally process wheat protein-based natural polymers with improved mechanical performance and water-resistant properties. PMID:19447383

  18. The utility of phenol-aldehyde cross linking resins in polymer modified asphalt - the Butaphalt (tm) process

    SciTech Connect

    Krivohlavek, D.D.

    1996-12-31

    The use of Phenol-Aldehyde cross linking or vulcanizing resin is well known in the rubber and plastics industry. Previous to our work little (if any) understanding of the utility of these compounds in polymer modified asphalt (or bitumen) was known. This presentation will hopefully enlighten practitioners of the art of asphalt modification on this subject. This art is commercially known as the Butaphalt(tm) Process. Of initial interest is the mechanism of reaction of Phenol-Aldehyde cross linking resins. As the quantitative analysis of such a mechanism in asphalt would likely need years of effort to resolve, we will look at possible mechanisms in a rubber system.

  19. Preparation of polymer-coated, scintillating ion-exchange resins for monitoring of 99Tc in groundwater.

    PubMed

    Seliman, Ayman F; Samadi, Azadeh; Husson, Scott M; Borai, Emad H; DeVol, Timothy A

    2011-06-15

    The present study was oriented to prepare new scintillating anion-exchange resins for measurement of (99)TcO(4)(-) in natural waters. The organic fluor 2-(1-naphthyl)-5-phenyloxazole was diffused into (chloromethyl)polystyrene resin. Thereafter, a thin layer of poly[[2-(methacryloyloxy)ethyl]trimethylammonium chloride] was grafted from the resin surface by surface-initiated atom transfer radical polymerization as an attempt to overcome potential problems related to the leaching of fluor molecules during usage. The residual chloromethyl groups of the polymer-coated resin were aminated by reaction with two different tertiary amines, triethylamine (TEA) and methyldioctylamine (MDOA). Off- and on-line quantification of (99)Tc was achieved with high detection efficiencies of 60.72 ± 1.93% and 72.83 ± 0.81% for resin with TEA and MDOA functional groups, respectively. The detection limit was determined to be less than the maximum contaminant level (33 Bq L(-1)) established under the Safe Drinking Water Act. The two functionalized resins were demonstrated to be selective for pertechnetate from synthetic groundwater containing up to 1000 ppm Cl(-), SO(4)(2-), and HCO(3)(-) and up to 1200 ppb Cr(2)O(7)(2-) in an acidic medium. PMID:21609030

  20. Synthesis of polymer nanocomposites by UV-curing of silver nano particles-acrylic resins

    NASA Astrophysics Data System (ADS)

    Balan, L.; Schneider, R.; Soppera, O.; Lougnot, D. J.

    2007-09-01

    We present here a simple method to synthesize organic-dispersible colloids and a scenario for the ultra-fast fabrication of silver/polymer nanocomposite by light-induced crosslinking polymerization. The objective of this work was to apply UV-curing technology for the fabrication of nanocomposite materials containing silver nanoparticles dispersed in a polymer binder. This new route allows processing operations to be simplified and the properties of the final product to be improved. A special attention has been paid to the synthesis and dispersion of metal nanoparticles in various monomers and oligomers and to the photopolymerization kinetics. The silver nanoparticles were generated by reduction of AgNO 3 with t-BuONa activated sodium hydride. Ag(0) particles present a narrow size distribution with an average diameter of 6.5 nm. Transmission electron microscopy (TEM) analysis has shown that Ag(0) nanoparticles are well dispersed in the acrylic resin. The curing process was followed quantitatively by FTIR spectroscopy through the decrease upon UV exposure of the IR bands characteristic of the functional groups. The silver nanoparticles have no detrimental effect on the photopolymerization kinetics. The incorporation of metal nanoparticles was found to greatly reduce the gloss of UV-cured coatings. Moreover, the outstanding optical and viscoelastic properties of these UV-cured nanocomposites opens up interesting perspectives in various fields of applications (optics, nanoelectronic, biology...).

  1. Column studies for the adsorption of cationic surfactant onto an organic polymer resin and a granular activated carbon.

    PubMed

    Vergili, Ilda; Kaya, Yasemin; Gönder, Zeren Beril; Barlas, Hulusi

    2010-03-01

    Adsorption beds containing granular activated carbon and organic polymer resin are used widely to remove organic pollutants from wastewaters and water streams. Adsorption polymers are becoming alternatives to activated carbon for removal of surfactants by adsorption techniques. This study investigated the adsorption characteristics of cetyl trimethylammonium bromide (CTAB) as a cationic surfactant for selected concentrations below and above critical micelle concentration (CMC). A series of column tests were performed to determine the breakthrough curves by using two different adsorbents: (1) Hydraffin CC 8 x 30 as a commercial granular activated carbon (GAC) and (2) Lewatit VPOC 1064 MD PH as a commercial organic polymer resin. In the experiments, the volumetric flow rate was maintained at 10.5 mL/min (approximately 2 m3/ m2 x h). Loading of adsorbents was continued until breakthrough was 10% of the feed concentration. The breakthrough took place at 488 bed volume (BV) below CMC (C0 = 40 mg/L) and 39 BV above CMC (C0 = 400 mg/ L) onto GAC. The organic polymer resin, however, showed a higher adsorption capacity than GAC (1412 BV below CMC and 287 BV above CMC). From the Logit method, the value of adsorption rate coefficient (K) and adsorption capacity coefficient (N) were obtained. PMID:20369564

  2. A positron annihilation study on the microstructure of the interpenetration polymer networks of cyanate ester resin/epoxy resin

    NASA Astrophysics Data System (ADS)

    Chenze, Qi; Chunqing, Li; Minfeng, Zeng; Baoyi, Wang; Jian, Zhang

    2010-04-01

    Cyanate ester (CE) resin was blended with epoxy resin (EP) at different mass ratios (CE/EP: 100/0, 90/10, 70/30, 50/50, 30/70, 10/90, 0/100). The free volume size of CE/EP IPNs has been determined by positron annihilation lifetime spectroscopy (PALS). The size decreased as the epoxy resin content increased. The PALS results are consistent with the chemical structure changes for the copolymerizing between CE and EP. The crosslinking units of curing products (oxazoline, oxazolidinone, and polyether network) of the blends are all smaller in size than those of triazine ring structure from neat CE. Therefore, the free volume size of the blends decreases with increase of EP content. Examination of the mechanical properties, thermal stability, and morphology of the blend systems showed that addition of epoxy resin resulted in improved toughness but a little sacrifice in thermal stability when compared with pure CE. The correlations between the free volume properties and physical properties (thermal stability and mechanical properties) have been discussed.

  3. Reduced toxicity polyester resins and microvascular pre-preg tapes for advanced composites manufacturing

    NASA Astrophysics Data System (ADS)

    Poillucci, Richard

    Advanced composites manufacturing broadly encapsulates topics ranging from matrix chemistries to automated machines that lay-up fiber-reinforced materials. Environmental regulations are stimulating research to reduce matrix resin formulation toxicity. At present, composites fabricated with polyester resins expose workers to the risk of contact with and inhalation of styrene monomer, which is a potential carcinogen, neurotoxin, and respiratory irritant. The first primary goal of this thesis is to reduce the toxicity associated with polyester resins by: (1) identification of potential monomers to replace styrene, (2) determination of monomer solubility within the polyester, and (3) investigation of approaches to rapidly screen a large resin composition parameter space. Monomers are identified based on their ability to react with polyester and their toxicity as determined by the Globally Harmonized System (GHS) and a green screen method. Solubilities were determined by the Hoftyzer -- Van Krevelen method, Hansen solubility parameter database, and experimental mixing of monomers. A combinatorial microfluidic mixing device is designed and tested to obtain distinct resin compositions from two input chemistries. The push for safer materials is complemented by a thrust for multifunctional composites. The second primary goal of this thesis is to design and implement the manufacture of sacrificial fiber materials suitable for use in automated fiber placement of microvascaular multifunctional composites. Two key advancements are required to achieve this goal: (1) development of a roll-to-roll method to place sacrificial fibers onto carbon fiber pre-preg tape; and (2) demonstration of feasible manufacture of microvascular carbon fiber plates with automated fiber placement. An automated method for placing sacrificial fibers onto carbon fiber tapes is designed and a prototype implemented. Carbon fiber tows with manual placement of sacrificial fibers is implemented within an

  4. Resin Flow of an Advanced Grid-Stiffened Composite Structure in the Co-Curing Process

    NASA Astrophysics Data System (ADS)

    Huang, Qizhong; Ren, Mingfa; Chen, Haoran

    2013-06-01

    The soft-mold aided co-curing process which cures the skin part and ribs part simultaneously was introduced for reducing the cost of advanced grid-stiffened composite structure (AGS). The co-curing process for a typical AGS, preformed by the prepreg AS4/3501-6, was simulated by a finite element program incorporated with the user-subroutines `thermo-chemical' module and the `chemical-flow' module. The variations of temperature, cure degree, resin pressure and fiber volume fraction of the AGS were predicted. It shows that the uniform distributions of temperature, cure degree and viscosity in the AGS would be disturbed by the unique geometrical pattern of AGS. There is an alternation in distribution of resin pressure at the interface between ribs and skin, and the duration time of resin flow is sensitive to the thickness of the AGS. To obtain a desired AGS, the process parameters of the co-curing process should be determined by the geometry of an AGS and the kinds of resin.

  5. Advanced polymer chemistry of organometallic anions

    SciTech Connect

    Chamberlin, R.M.; Abney, K.D.; Balaich, G.J.; Fino, S.A.

    1997-11-01

    This is the final report of a one-year, Laboratory Directed Research and Development (LDRD) project at the Los Alamos National Laboratory (LANL). The objective of the project was to prepare and characterize new polymers incorporating cobalt dicarbollide. Specific goals were to prepare polymerizable cobalt dicarbollide monomers using the nucleophilic substitution route discovered in laboratories and to establish the reaction conditions required to form polymers from these complexes. This one-year project resulted in two publications (in press), and provided the foundation for further investigations into polymer synthesis and characterization using cobalt dicarbollide and other metallocarboranes. Interest in synthesizing organometallic polymers containing the cobalt bis(dicarbollide) anion is motivated by their possible application as cation exchange materials for the remediation of cesium-137 and strontium-90 from nuclear wastes.

  6. Advanced materials based on polymer blends/polymer blend nanocomposites

    NASA Astrophysics Data System (ADS)

    Shikaleska, A. V.; Pavlovska, F. P.

    2012-09-01

    Processability, morphology, mechanical properties and rheological behavior of poly(vinylchloride) (PVC)/poly(ethylmethacrylate) (PEMA) blends and PVC/PEMA/montmorillonite (MMT) composites, prepared by melt processing in a brabender mixer, were studied. Samples were characterized using SEM, mechanical testing, DMTA and a parallel plate rheometer. Plastograms show that there is noticeable drop of fusion times and increase in melt viscosity torque of both, polymer blend and polymer blend nanocomposite, in comparison with those of neat PVC. SEM images show that homogenous dispersions are obtained. Tensile tests indicate that PVC/PEMA and PVC/PEMA/MMT samples have greater tensile strength and elastic modulus and lower elongation compared to PVC. When solid viscoelastic properties are considered (DMTA), slightly higher storage moduli are obtained whereas more prominent increase of storage modulus is observed when nanoclay particles are added in a PVC/PEMA matrix. From the calculated area of tandelta peak of all tested samples, nanocomposites exhibit the lowest damping behavior. Oscillatory measurements in a molten state were used for determining the frequency dependencies of storage G' and loss G" moduli. It was found that G" curves of neat PVC lie above those of G' suggesting that PVC behaves like viscoelastic liquid. Similar results, but with significantly higher values of G' and G" over the whole frequency range for PVC/PEMA blends were obtained. Steady shear measurements show that the presence of PEMA and nanoclay particles increases the shear stress and shear viscosity of neat PVC. In order to define the rheological equations of state the three material functions were determined. According to these functions all samples exhibit shear thinning behavior and the curves obey the power law equation. As rheological behaviour was found to be strongly dependent on blend's micro and macro structure and it is one of the main factors defining the end properties, attempt was

  7. Polymer, metal and ceramic matrix composites for advanced aircraft engine applications

    NASA Technical Reports Server (NTRS)

    Mcdanels, D. L.; Serafini, T. T.; Dicarlo, J. A.

    1985-01-01

    Advanced aircraft engine research within NASA Lewis is being focused on propulsion systems for subsonic, supersonic, and hypersonic aircraft. Each of these flight regimes requires different types of engines, but all require advanced materials to meet their goals of performance, thrust-to-weight ratio, and fuel efficiency. The high strength/weight and stiffness/weight properties of resin, metal, and ceramic matrix composites will play an increasingly key role in meeting these performance requirements. At NASA Lewis, research is ongoing to apply graphite/polyimide composites to engine components and to develop polymer matrices with higher operating temperature capabilities. Metal matrix composites, using magnesium, aluminum, titanium, and superalloy matrices, are being developed for application to static and rotating engine components, as well as for space applications, over a broad temperature range. Ceramic matrix composites are also being examined to increase the toughness and reliability of ceramics for application to high-temperature engine structures and components.

  8. Polymer resins with amino acid containing pendants for sorption of bilirubin. II. Polyamide resins with various basic amino acids.

    PubMed

    Henning, D S; Brown, G R; St-Pierre, L E

    1986-01-01

    Short peptides, three to eight amino acids in length, containing various combinations of alanine, arginine, lysine, histidine and tyrosine have been synthesized onto water-swellable polyamide resin by the solid phase peptide synthesis method. The amount of bilirubin adsorbed from aqueous buffer solution (pH = 7.8) by the resins increases with increasing basicity of the amino acids in the pendant. As the number of basic amino acids on the pendant is increased from one to five a 4.7 fold enhancement in the adsorption capacity is seen for arginine while a 9.3 fold enhancement is obtained for lysine. A corresponding increase in length for the non-basic histidine results in a 6 fold enhancement. With alanine the adsorption capacity is uneffected by an increase in pendant length. PMID:3957453

  9. Thermosetting polyimide resin matrix composites with interpenetrating polymer networks for precision foil resistor chips based on special mechanical performance requirements

    NASA Astrophysics Data System (ADS)

    Wang, X. Y.; Ma, J. X.; Li, C. G.; Wang, H. X.

    2014-04-01

    Based on interpenetrating networks (IPNs) different macromolecular materials such as epoxy, phenolic, and silicone resin were chosen to modify thermosetting polyimide (TSPI) resin to solve the lack of performance when used for protecting precision foil resistor chips. Copolymerization modification, controlled at curing stage, was used to prepare TSPI composites considering both performance and process requirements. The mechanical properties related to trimming process were mainly studied due to the special requirements of the regularity of scratch edges caused by a tungsten needle. The analysis on scratch edges reveals that the generation and propagation of microcracks caused by scratching together with crack closure effect may lead to regular scratch traces. Experiments show that the elongation at break of TSPI composites is the main reason that determines the special mechanical properties. The desired candidate materials should have proper hardness and toughness, and the specific mechanical data are that the mean elongation at break and tensile strength of polymer materials are in the range of 9.2-10.4% and 100-107 MPa, respectively. Possible reasons for the effect of the modifiers chosen on TSPI polymers, the reaction mechanisms on modified TSPI resin and the IPN structure in TSPI composite polymers were discussed based on IR and TG analysis.

  10. Recent advances in conjugated polymers for light emitting devices.

    PubMed

    Alsalhi, Mohamad Saleh; Alam, Javed; Dass, Lawrence Arockiasamy; Raja, Mohan

    2011-01-01

    A recent advance in the field of light emitting polymers has been the discovery of electroluminescent conjugated polymers, that is, kind of fluorescent polymers that emit light when excited by the flow of an electric current. These new generation fluorescent materials may now challenge the domination by inorganic semiconductor materials of the commercial market in light-emitting devices such as light-emitting diodes (LED) and polymer laser devices. This review provides information on unique properties of conjugated polymers and how they have been optimized to generate these properties. The review is organized in three sections focusing on the major advances in light emitting materials, recent literature survey and understanding the desirable properties as well as modern solid state lighting and displays. Recently, developed conjugated polymers are also functioning as roll-up displays for computers and mobile phones, flexible solar panels for power portable equipment as well as organic light emitting diodes in displays, in which television screens, luminous traffic, information signs, and light-emitting wallpaper in homes are also expected to broaden the use of conjugated polymers as light emitting polymers. The purpose of this review paper is to examine conjugated polymers in light emitting diodes (LEDs) in addition to organic solid state laser. Furthermore, since conjugated polymers have been approved as light-emitting organic materials similar to inorganic semiconductors, it is clear to motivate these organic light-emitting devices (OLEDs) and organic lasers for modern lighting in terms of energy saving ability. In addition, future aspects of conjugated polymers in LEDs were also highlighted in this review. PMID:21673938

  11. Recent Advances in Conjugated Polymers for Light Emitting Devices

    PubMed Central

    AlSalhi, Mohamad Saleh; Alam, Javed; Dass, Lawrence Arockiasamy; Raja, Mohan

    2011-01-01

    A recent advance in the field of light emitting polymers has been the discovery of electroluminescent conjugated polymers, that is, kind of fluorescent polymers that emit light when excited by the flow of an electric current. These new generation fluorescent materials may now challenge the domination by inorganic semiconductor materials of the commercial market in light-emitting devices such as light-emitting diodes (LED) and polymer laser devices. This review provides information on unique properties of conjugated polymers and how they have been optimized to generate these properties. The review is organized in three sections focusing on the major advances in light emitting materials, recent literature survey and understanding the desirable properties as well as modern solid state lighting and displays. Recently, developed conjugated polymers are also functioning as roll-up displays for computers and mobile phones, flexible solar panels for power portable equipment as well as organic light emitting diodes in displays, in which television screens, luminous traffic, information signs, and light-emitting wallpaper in homes are also expected to broaden the use of conjugated polymers as light emitting polymers. The purpose of this review paper is to examine conjugated polymers in light emitting diodes (LEDs) in addition to organic solid state laser. Furthermore, since conjugated polymers have been approved as light-emitting organic materials similar to inorganic semiconductors, it is clear to motivate these organic light-emitting devices (OLEDs) and organic lasers for modern lighting in terms of energy saving ability. In addition, future aspects of conjugated polymers in LEDs were also highlighted in this review. PMID:21673938

  12. Insulating polymer concrete. [Perlite or glass nodule aggregates bound together with a polyester resin

    SciTech Connect

    Fontana, J.J.

    1984-04-01

    An insulating polymer concrete (IPC) composite has been developed under contract to the Gas Research Institute for possible use as a dike insulation material at Liquid Natural Gas (LNG) storage facilities. In the advent of an LNG spill into the impounding dike area, the boiloff rate of the LNG can be substantially reduced if the surfaces of the dike are insulated. This increased safety at the LNG facility will tend to reduce the hazardous explosive mixture with atmospheric air in the surrounding region. The dike insulation material must have a low thermal conductivity and be unaffected by environmental conditions. The IPC composites developed consist of perlite or glass nodule aggregates bound together as a closed cell structure with a polyester resin. In addition to low thermal conductivity and porosity, these composites have correspondingly high strengths and, therefore, can carry transient loads of workmen and maintenance equipment. Prefabricated IPC panels have been installed experimentally and at least one utility is currently considering a complete installation at its LNG facility. 4 references, 8 tables.

  13. Amino resin modified xanthan polymer foamed with a chemical blowing agent

    SciTech Connect

    Hazlett, R.D.; Shu, P.

    1989-05-16

    A method is described for reducing the permeability in an area of a subterranean formation which consists of mixing a gellable composition containing: water, about 0.2 to about 5.0 wt.% of a cross linkable polysaccharide biopolymer having at least one functional group charide biopolymer having at least one functional group selected from a member of the group consisting of an amine, an amide, a hydroxyl, or a thiol group, and about 0.02 to about 5.0 wt.% of an aminoplast resin which reinforces the biopolymer thereby causing the polymer to become more thermally stable. Also included are sufficient transitional metal ions to form a gel of a size and strength sufficient to reduce permeability in a more permeable zone in the formation. A chemical surfactant, and an alkali metal salt of azodicarboxylic acid, are then introduced produce a gas sufficient to foam the composition described above. The composition is then injected into the desired area of the formation where the azodicarboxylic acid decomposes thereby generating nitrogen and carbon dioxide gas in an amount sufficient to form a foam which subsequently hardens and reduces the permeability in the desired area.

  14. Advanced Polymer For Multilayer Insulating Blankets

    NASA Technical Reports Server (NTRS)

    Haghighat, R. Ross; Shepp, Allan

    1996-01-01

    Polymer resisting degradation by monatomic oxygen undergoing commercial development under trade name "Aorimide" ("atomic-oxygen-resistant imidazole"). Intended for use in thermal blankets for spacecraft in low orbit, useful on Earth in outdoor applications in which sunlight and ozone degrades other plastics. Also used, for example, to make threads and to make films coated with metals for reflectivity.

  15. Advancing polymers of intrinsic microporosity by mechanochemistry

    DOE PAGESBeta

    Zhang, Pengfei; Jiang, Xueguang; Wan, Shun; Dai, Sheng

    2015-02-20

    Herein, we report a fast (15 min) and solvent-free mechanochemical approach to construct polymers of intrinsic microporosity (PIMs) with high molecular mass and low polydispersity by solid grinding. The enhanced reaction efficiency results from the instantaneous frictional heating and continuous exposure of active sites within those solid reactants.

  16. Polymer-brush lubrication: a review of recent theoretical advances.

    PubMed

    Kreer, T

    2016-04-13

    This review compiles recent theoretical advances to describe compressive and shear forces of polymer-brush bilayers, which consist of two opposing brushes in contact. Such model systems for polymer-brush lubrication are frequently used as a benchmark to gain insight into biological problems, e.g., synovial joint lubrication. Based on scaling theory, I derive conformational and collective properties of polymer-brush bilayers in equilibrium and out-of-equilibrium situations, such as shear forces in the linear and nonlinear response regimes of stationary shear and under non-stationary shear. Furthermore, I discuss the influence of macromolecular inclusions and electrostatic interactions on polymer-brush lubrication. Comparisons to alternative analytical approaches, experiments and numerical results are performed. Special emphasis is given to methods for simulating polymer-brush bilayers using molecular dynamics simulations. PMID:27029521

  17. Polymer infiltration studies

    NASA Technical Reports Server (NTRS)

    Marchello, Joseph M.

    1992-01-01

    The preparation is reported of carbon fiber composites using advanced polymer resins. Current and ongoing research activities include: powder towpreg process; weaving, braiding and stitching dry powder prepreg; advanced tow placement; and customized ATP towpreg. The goal of these studies is to produce advanced composite materials for automated part fabrication using textile and robotics technology in the manufacture of subsonic and supersonic aircraft.

  18. Advanced Developments in Cyclic Polymers: Synthesis, Applications, and Perspectives

    PubMed Central

    Zhu, Yinghuai; Hosmane, Narayan S

    2015-01-01

    Due to the topological effect, cyclic polymers demonstrate different and unique physical and biological properties in comparison with linear counterparts having the same molecular-weight range. With advanced synthetic and analytic technologies, cyclic polymers with different topologies, e.g. multicyclic polymers, have been reported and well characterized. For example, various cyclic DNA and related structures, such as cyclic duplexes, have been prepared conveniently by click chemistry. These types of DNA have increased resistance to enzymatic degradation and have high thermodynamic stability, and thus, have potential therapeutic applications. In addition, cyclic polymers have also been used to prepare organic–inorganic hybrids for applications in catalysis, e.g. catalyst supports. Due to developments in synthetic technology, highly pure cyclic polymers could now be produced in large scale. Therefore, we anticipate discovering more applications in the near future. Despite their promise, cyclic polymers are still less explored than linear polymers like polyolefins and polycarbonates, which are widely used in daily life. Some critical issues, including controlling the molecular weight and finding suitable applications, remain big challenges in the cyclic-polymer field. This review briefly summarizes the commonly used synthetic methodologies and focuses more on the attractive functional materials and their biological properties and potential applications. PMID:26478835

  19. Chromium Ions Improve Moisure Resistance of Epoxy Resins

    NASA Technical Reports Server (NTRS)

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

    1986-01-01

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

  20. High-temperature polymer matrix composites

    NASA Technical Reports Server (NTRS)

    Meador, Michael A.

    1990-01-01

    Polymers research at the NASA Lewis Research Center has produced high-temperature, easily processable resin systems, such as PMR-15. In addition, the Polymers Branch has investigated ways to improve the mechanical properties of polymers and the microcracking resistance of polymer matrix composites in response to industry need for new and improved aeropropulsion materials. Current and future research in the Polymers Branch is aimed at advancing the upper use temperature of polymer matrix composites to 700 F and beyond by developing new resins, by examining the use of fiber reinforcements other than graphite, and by developing coatings for polymer matrix composites to increase their oxidation resistance.

  1. Advances in Polymer and Polymeric Nanostructures for Protein Conjugation

    PubMed Central

    González-Toro, Daniella C.; Thayumanavan, S.

    2013-01-01

    Linear polymers have been considered the best molecular structures for the formation of efficient protein conjugates due to their biological advantages, synthetic convenience and ease of functionalization. In recent years, much attention has been dedicated to develop synthetic strategies that produce the most control over protein conjugation utilizing linear polymers as scaffolds. As a result, different conjugate models, such as semitelechelic, homotelechelic, heterotelechelic and branched or star polymer conjugates, have been obtained that take advantage of these well-controlled synthetic strategies. Development of protein conjugates using nanostructures and the formation of said nanostructures from protein-polymer bioconjugates are other areas in the protein bioconjugation field. Although several polymer-protein technologies have been developed from these discoveries, few review articles have focused on the design and function of these polymers and nanostructures. This review will highlight some recent advances in protein-linear polymer technologies that employ protein covalent conjugation and successful protein-nanostructure bioconjugates (covalent conjugation as well) that have shown great potential for biological applications. PMID:24058205

  2. Development of advanced polymer nanocomposite capacitors

    NASA Astrophysics Data System (ADS)

    Mendoza, Miguel

    The current development of modern electronics has driven the need for new series of energy storage devices with higher energy density and faster charge/discharge rate. Batteries and capacitors are two of the most widely used energy storage devices. Compared with batteries, capacitors have higher power density and significant higher charge/discharge rate. Therefore, high energy density capacitors play a significant role in modern electronic devices, power applications, space flight technologies, hybrid electric vehicles, portable defibrillators, and pulse power applications. Dielectric film capacitors represent an exceptional alternative for developing high energy density capacitors due to their high dielectric constants, outstanding breakdown voltages, and flexibility. The implementation of high aspect ratio dielectric inclusions such as nanowires into polymer capacitors could lead to further enhancement of its energy density. Therefore, this research effort is focused on the development of a new series of dielectric capacitors composed of nanowire reinforced polymer matrix composites. This concept of nanocomposite capacitors combines the extraordinary physical and chemical properties of the one-dimension (1D) nanoceramics and high dielectric strength of polymer matrices, leading to a capacitor with improved dielectric properties and energy density. Lead-free sodium niobate (NaNbO3) and lead-containing lead magnesium niobate-lead titanate (0.65PMN-0.35PT) nanowires were synthesized following hydrothermal and sol-gel approaches, respectively. The as-prepared nanowires were mixed with a polyvinylidene fluoride (PVDF) matrix using solution-casting method for nanocomposites fabrication. The dielectric constants and breakdown voltages of the NaNbO3/PVDF and 0.65PMN-0.35PT/PVDF nanocomposites were measured under different frequency ranges and temperatures in order to determine their maximum energy (J/cm3) and specific (J/g) densities. The electrical properties of the

  3. Advanced composite polymer electrolyte fuel cell membranes

    SciTech Connect

    Wilson, M.S.; Zawodzinski, T.A.; Gottesfeld, S.; Kolde, J.A.; Bahar, B.

    1995-09-01

    A new type of reinforced composite perfluorinated polymer electrolyte membrane, GORE-SELECT{trademark} (W.L. Gore & Assoc.), is characterized and tested for fuel cell applications. Very thin membranes (5-20 {mu}m thick) are available. The combination of reinforcement and thinness provides high membrane, conductances (80 S/cm{sup 2} for a 12 {mu}m thick membrane at 25{degrees}C) and improved water distribution in the operating fuel cell without sacrificing longevity or durability. In contrast to nonreinforced perfluorinated membranes, the x-y dimensions of the GORE-SELECT membranes are relatively unaffected by the hydration state. This feature may be important from the viewpoints of membrane/electrode interface stability and fuel cell manufacturability.

  4. Infiltration/cure modeling of resin transfer molded composite materials using advanced fiber architectures

    NASA Technical Reports Server (NTRS)

    Loos, Alfred C.; Weideman, Mark H.; Long, Edward R., Jr.; Kranbuehl, David E.; Kinsley, Philip J.; Hart, Sean M.

    1991-01-01

    A model was developed which can be used to simulate infiltration and cure of textile composites by resin transfer molding. Fabric preforms were resin infiltrated and cured using model generated optimized one-step infiltration/cure protocols. Frequency dependent electromagnetic sensing (FDEMS) was used to monitor in situ resin infiltration and cure during processing. FDEMS measurements of infiltration time, resin viscosity, and resin degree of cure agreed well with values predicted by the simulation model. Textile composites fabricated using a one-step infiltration/cure procedure were uniformly resin impregnated and void free. Fiber volume fraction measurements by the resin digestion method compared well with values predicted using the model.

  5. RAFT technology for the production of advanced photoresist polymers

    NASA Astrophysics Data System (ADS)

    Sheehan, Michael T.; Farnham, William B.; Okazaki, Hiroshi; Sounik, James R.; Clark, George

    2008-03-01

    Reversible Addition Fragmentation Chain Transfer (RAFT) technology has been developed for use in producing high yield low polydispersity (PD) polymers for many applications. RAFT technology is being used to produce low PD polymers and to allow control of the polymer architecture. A variety of polymers are being synthesized for use in advanced photoresists using this technique. By varying the RAFT reagent used we can modulate the system reactivity of the RAFT reagent and optimize it for use in acrylate or methacrylate monomer systems (193 and 193i photoresist polymers) or for use in styrenic monomer systems (248 nm photoresist polymers) to achieve PD as low as 1.05. RAFT polymerization technology also allows us to produce block copolymers using a wide variety of monomers. These block copolymers have been shown to be useful in self assembly polymer applications to produce unique and very small feature sizes. The mutual compatibilities of all the components within a single layer 193 photoresist are very important in order to achieve low LWR and low defect count. The advent of immersion imaging demands an additional element of protection at the solid/liquid interface. We have used RAFT technology to produce block copolymers comprising a random "resist" block with composition and size based on conventional dry photoresist materials, and a "low surface energy" block for use in 193i lithography. The relative block lengths and compositions may be varied to tune solution behavior, surface energy, contact angles, and solubility in developer. The use of this technique will be explored to produce polymers used in hydrophobic single layer resists as well as additives compatible with the main photoresist polymer.

  6. Polymer radiation curing: polyester resins. January 1973-December 1988 (Citations from the Rubber and Plastics Research Association data base). Report for January 1973-December 1988

    SciTech Connect

    Not Available

    1989-01-01

    This bibliography contains citations concerning the formulations and processes for radiation curing on polyester resins. Effects of radiation curing on polyester resins are also discussed. Electron-beam and ultraviolet radiation are emphasized. Polymer crosslinking by such electromagnetic wave radiation as in the visible wavelength is also examined. Applications in adhesives, coatings, lacquers, and printing inks are included. (Contains 200 citations fully indexed and including a title list.)

  7. IUPAC International Symposium on Polymers for Advanced Technologies, Jerusalem, Israel, Aug. 16-21, 1987, Proceedings

    SciTech Connect

    Lewin, M.

    1988-01-01

    The present conference discusses topics in radiation-sensitive, radiation-modified, and cured polymers, polymers of photoconductive, electroconductive, and piezoelectric type, polymers for advanced structures, liquid-crystal polymers, high-performance polymers compounded from flexible macromolecules, polymer networks, polymer blends, and the matching of composites with adhesives. Attention is given to the industrial radiation-curing of polymers, a frequency-analysis of ferroelectricity, liquid crystal polyester fibers, photochromic and thermochromic liquid crystals, diacetylene-based single-crystal fibers, interpenetrating polymer networks, chain-length development in complex epoxy-amine matrices, and a statistical-thermodynamic theory of polymer precipitation fractionation.

  8. Polymer grafted hydroxyapatite whisker as a filler for dental composite resin with enhanced physical and mechanical properties.

    PubMed

    Liu, Fengwei; Wang, Ruili; Cheng, Yanhua; Jiang, Xiaoze; Zhang, Qinghong; Zhu, Meifang

    2013-12-01

    The objective of this study was to investigate the effect of surface graft polymerization of hydroxyapatite whisker (HW) on physical and mechanical properties of dental composite resin. Poly bisphenol A glycidyl methacrylate (Poly(Bis-GMA)) was grafted onto silanized hydroxyapatite whisker (SHW) via solution polymerization and the amount of the Poly(Bis-GMA) on the surface was effectively controlled by polymerization time. The obtained poly(Bis-GMA) grafted hydroxyapatite whisker (PGHW) with different polymer contents was filled into a resin matrix respectively, meanwhile the composites with HW and with SHW served as controls. Monomer conversion was characterized by Fourier transform infrared spectroscopy (FTIR) and volume shrinkage of the composite resin was measured with a density tester. Mechanical properties were tested with a universal testing machine. The results indicated that the composite filled with PGHW-1h (graft ratio of poly(Bis-GMA): 8.5 wt.%) showed lower shrinkage and better mechanical properties, improving flexural strength by 6.5% and 11.9% compared with SHW filled composite and HW filled composite, respectively. However, PGHW with higher graft ratios aggregated seriously and formed defects in the composite, leading to deterioration of mechanical properties. It was revealed that the poly(Bis-GMA) on the surface of PGHW acted as a functional transition layer and enhanced interfacial compatibility and interaction between whisker and resin matrix, which facilitated the dispersion of PGHW in the composite and decreased the composite shrinkage. Thus, the graft polymerization of Bis-GMA on the surface of filler might be a promising modification method for the fabrication of dental materials. PMID:24094216

  9. Bridging Microstructure, Properties and Processing of Polymer Based Advanced Materials

    SciTech Connect

    Li, Dongsheng; Ahzi, Said; Khaleel, Mohammad A.

    2012-01-01

    This is a guest editorial for a special issue in Journal of Engineering Materials and Technology. The papers collected in this special issue emphasize significant challenges, current approaches and future strategies necessary to advance the development of polymer-based materials. They were partly presented at the symposium of 'Bridging microstructure, properties and processing of polymer based advanced materials' in the TMS 2011 annual conference meeting, which was held in San Diego, US, on Feb 28 to March 3, 2011. This symposium was organized by the Pacific Northwest National Laboratory (USA) and the Institute of Mechanics of Fluids and Solids of the University of Strasbourg (France). The organizers were D.S. Li, S. Ahzi, and M. Khaleel.

  10. Advanced Composites: Mechanical Properties and Hardware Programs for Selected Resin Matrix Materials. [considering space shuttle applications

    NASA Technical Reports Server (NTRS)

    Welhart, E. K.

    1976-01-01

    This design note presents typical mechanical properties tabulated from industrial and governmental agencies' test programs. All data are correlated to specific products and all of the best known products are presented. The data include six epoxies, eight polyimides and one polyquinoxaline matrix material. Bron and graphite are the fiber reinforcements. Included are forty-two summaries of advanced (resin matrix) composite programs in existence in the United States. It is concluded that the selection of appropriate matrices, the geometric manner in which the fibers are incorporated in the matrix and the durability of the bond between fiber and matrix establish the end properties of the composite material and the performance of the fabricated structure.

  11. Sub-0.25-μm i-line photoresist: the role of advanced resin technology

    NASA Astrophysics Data System (ADS)

    Xu, Cheng-Bai; Zampini, Anthony; Sandford, Harold F.; Lachowski, Joseph; Carmody, Judy

    1999-06-01

    The use of di-functional monomers such as 2,6- Bis(hydroxymethyl)-p-cresol has allowed the design of novolak resins having alternating architecture with enhanced o,o'-bonding order, specific end-groups and narrow molecular weight distribution. When compared with a conventional m-/p- cresol formaldehyde novolak, the new resins have a lower molecular weight and molecular weight distribution with no p-cresol enriched oligomer fractions. Generally, these resins are used without further processing. With the proper monomer selection novolak resins can be made with the appropriate hydrophilic balance and dissolution characteristics essential for advanced resist development and optimization. By coupling the resin properties with the properties of diazonaphthoquinone sulfonate esters that have a high resolution potential, two advanced sub 0.25 micrometers i- line resist prototypes were developed. With annular illumination, Resist Prototype I demonstrated excellent linear resolution of 0.22 micrometers and an exceptional focus latitude of 1.4 micrometers and 1.7 micrometers for the 0.23 micrometers and 0.25 micrometers dense L/S, respectively; while Resist Prototype II showed linear resolution of 0.18 micrometers L/S and outstanding focus latitudes of 1.6 micrometers and 1.7 micrometers for the 0.21 micrometers L/S and the 0.23 micrometers L/S, respectively.

  12. Recent Advances in Conjugated Polymer Materials for Disease Diagnosis.

    PubMed

    Lv, Fengting; Qiu, Tian; Liu, Libing; Ying, Jianming; Wang, Shu

    2016-02-10

    The extraordinary optical amplification and light-harvesting properties of conjugated polymers impart sensing systems with higher sensitivity, which meets the primary demands of early cancer diagnosis. Recent advances in the detection of DNA methylation and mutation with polyfluorene derivatives based fluorescence resonance energy transfer (FRET) as a means to modulate fluorescent responses attest to the great promise of conjugated polymers as powerful tools for the clinical diagnosis of diseases. To facilitate the ever-changing needs of diagnosis, the development of detection approaches and FRET signal analysis are highlighted in this review. Due to their exceptional brightness, excellent photostability, and low or absent toxicity, conjugated polymers are verified as superior materials for in-vivo imaging, and provide feasibility for future clinical molecular-imaging applications. The integration of conjugated polymers with clinical research has shown profound effects on diagnosis for the early detection of disease-related biomarkers, as well as in-vivo imaging, which leads to a multidisciplinary scientific field with perspectives in both basic research and application issues. PMID:26679834

  13. Advanced High Temperature Polymer Matrix Composites for Gas Turbine Engines Program Expansion

    NASA Technical Reports Server (NTRS)

    Hanley, David; Carella, John

    1999-01-01

    This document, submitted by AlliedSignal Engines (AE), a division of AlliedSignal Aerospace Company, presents the program final report for the Advanced High Temperature Polymer Matrix Composites for Gas Turbine Engines Program Expansion in compliance with data requirements in the statement of work, Contract No. NAS3-97003. This document includes: 1 -Technical Summary: a) Component Design, b) Manufacturing Process Selection, c) Vendor Selection, and d) Testing Validation: 2-Program Conclusion and Perspective. Also, see the Appendix at the back of this report. This report covers the program accomplishments from December 1, 1996, to August 24, 1998. The Advanced High Temperature PMC's for Gas Turbine Engines Program Expansion was a one year long, five task technical effort aimed at designing, fabricating and testing a turbine engine component using NASA's high temperature resin system AMB-21. The fiber material chosen was graphite T650-35, 3K, 8HS with UC-309 sizing. The first four tasks included component design and manufacturing, process selection, vendor selection, component fabrication and validation testing. The final task involved monthly financial and technical reports.

  14. Surface Response of Fluorine Polymer-Incorporated Resin Composites to Cariogenic Biofilm Adherence▿ †

    PubMed Central

    Gyo, Mariko; Nikaido, Toru; Okada, Koichi; Yamauchi, Junichi; Tagami, Junji; Matin, Khairul

    2008-01-01

    Experimental resin composites with incorporated polytetrafluoroethylene (PTFE) particles were developed, which theoretically could improve the surface properties of the materials, including the inhibition of bacterial adherence. To assess the surface properties in relation to biofilm formation and detachment, 23.1% (wt/wt) linear PTFE particles (FL-30) and cross-linked PTFE particles (FC-30) were incorporated into pure resin composites. Pure PTFE plates and pure resin composites without PTFE (F-0) were used as control specimens. Sucrose-dependent Streptococcus mutans biofilms were formed on the specimen blocks inside an oral biofilm reactor for various time periods and analyzed with or without application of driving forces. In addition, water contact angles and surface roughness were measured. The water contact angles of FL-30 (61.2°) and FC-30 (65.8°) were larger than that of F-0 (48.5°). The largest contact angle (107°) was detected on pure PTFE plates. However, the surfaces of FL-30, FC-30, and pure PTFE plates were rougher than that of F-0. Although the surface properties of the materials differed in terms of contact angles and roughness, these factors seemed not to affect biofilm formation on the surfaces within 5 h. Pure PTFE plates harbored almost the same amounts of biofilm as F-0. However, when a very strong driving force was applied, it was clear that there were significantly smaller amounts of biofilms retained on pure PTFE plates, which showed contact angles much higher than those of the other materials. Hydrophobicity of the resin composite was improved by incorporation of PTFE fillers. However, surface resistance against biofilm formation was not improved. PMID:18192415

  15. Advancements of molecularly imprinted polymers in the food safety field.

    PubMed

    Wang, Peilong; Sun, Xiaohua; Su, Xiaoou; Wang, Tie

    2016-06-01

    Molecularly imprinted technology (MIT) has been widely employed to produce stable, robust and cheap molecularly imprinted polymer (MIP) materials that possess selective binding sites for recognition of target analytes in food, such as pesticides, veterinary drugs, mycotoxins, illegal drugs and so on. Because of high selectivity and specificity, MIPs have drawn great attention in the food safety field. In this review, the recent developments of MIPs in various applications for food safety, including sample preparation, chromatographic separation, sensing, immunoassay etc., have been summarized. We particularly discuss the advancements and limitations in these applications, as well as attempts carried out for their improvement. PMID:26937495

  16. Recent advances in solid polymer electrolyte fuel cell technology

    SciTech Connect

    Ticianelli, E.A.; Srinivasan, S.; Gonzalez, E.R.

    1988-01-01

    With methods used to advance solid polymer electrolyte fuel cell technology, we are close to obtaining the goal of 1 A/cm/sup 2/ at 0.7. Higher power densities have been reported (2 A/cm/sup 2/ at 0.5 V) but only with high catalyst loading electrodes (2 mg/cm/sup 2/ and 4 mg/cm/sup 2/ at anode and cathode, respectively) and using a Dow membrane with a better conductivity and water retention characteristics. Work is in progress to ascertain performances of cells with Dow membrane impregnated electrodes and Dow membrane electrolytes. 5 refs., 6 figs.

  17. Addition polymers from 1,4,5,8-tetrahydro-1,4;5,8-diepoxyanthracene and Bis-dienes: Processable resins for high temperature application

    NASA Technical Reports Server (NTRS)

    Meador, Mary Ann B.

    1987-01-01

    1,4,5,8-Tetrahydro-1,4;5,8-diepoxyanthracene reacts with various anthracene endcapped polyimide oligomers to form Diels-Alder cycloaddition copolymers. The polymers are soluble in common organic solvents, and have molecular weights of approximately 21,000 to 32,000. Interestingly, these resins appear to be more stable in air then in nitrogen. This is shown to be due to a unique dehydration (loss of water ranges from 2 to 5 percent) at temperatures of 390 to 400 C to give thermo-oxidatively stable pentiptycene units along the polymer backbone. Because of their high softening points and good thermo-oxidative stability, the polymers have potential as processible, matrix resins for high temperature composite applications.

  18. Supramolecular polymer adhesives: advanced materials inspired by nature.

    PubMed

    Heinzmann, Christian; Weder, Christoph; de Espinosa, Lucas Montero

    2016-01-21

    Due to their dynamic, stimuli-responsive nature, non-covalent interactions represent versatile design elements that can be found in nature in many molecular processes or materials, where adaptive behavior or reversible connectivity is required. Examples include molecular recognition processes, which trigger biological responses or cell-adhesion to surfaces, and a broad range of animal secreted adhesives with environment-dependent properties. Such advanced functionalities have inspired researchers to employ similar design approaches for the development of synthetic polymers with stimuli-responsive properties. The utilization of non-covalent interactions for the design of adhesives with advanced functionalities such as stimuli responsiveness, bonding and debonding on demand capability, surface selectivity or recyclability is a rapidly emerging subset of this field, which is summarized in this review. PMID:26203784

  19. The modifications of epoxy resin and their crystalline polymer particle filled epoxies

    SciTech Connect

    Huei-Hsiung Wang

    1996-12-31

    The chemical linking of the modifier to the epoxy network was overcome by using Bisphenol A, 4,4`-diaminodiphenyl sulphone or benzophenone-tetracarboxylic dianhydride as a coupling agent between the PU and the epoxy oligomer. From the experimental results, it was shown that the values of fracture energy, G{sub IC} for PU-modified epoxy were dependent on the macroglycols and the coupling agents. Scanning electron microscopy and the glass transition temperature were used to assess the morphology and their compatibility of these modified epoxies. It revealed that the ether type (PTMG) of PU modified epoxy showed the present of an aggregated separated phase. However, the ester type (PBA) PU-modified epoxy resin showed a homogenous morphology. In addition, the {Beta}-relaxation of cured epoxy resin showed a more clear two-phase separation existed in Bis-A as a coupling agents. The additive of the semi-crystalline PBT powder was more efficient in fracture energies of epoxy network than that of the Nylon 6,6 powder.

  20. Fire and heat resistant laminating resins based on maleimido substituted aromatic cyclotriphosphazene polymer

    NASA Technical Reports Server (NTRS)

    Kumar, Devendra (Inventor); Fohlen, George M. (Inventor); Parker, John A. (Inventor)

    1987-01-01

    4-Aminophenoxy cyclotriphosphazenes are reacted with maleic anhydride to produce maleamic acids which are converted to the maleimides. The maleimides are polymerized. By selection of starting materials (e.g., hexakis amino or trisaminophenoxy trisphenoxy cyclotriphosphazenes), selection of molar proportions of reactants, use of mixtures of anhydrides and use of dianhydrides as bridging groups a variety of maleimides and polymers are produced. The polymers have high limiting oxygen indices, high char yields and other useful heat and fire resistant properties making them useful as, for example, impregnants of fabrics.

  1. Polymer infiltration studies

    NASA Technical Reports Server (NTRS)

    Marchello, Joseph M.

    1991-01-01

    Progress was made on the preparation of carbon fiber composites using advanced polymer resins. Processes reported include powder towpreg process, weaving towpreg made from dry powder prepreg, composite from powder coated towpreg, and toughening of polyimide resin (PMR) composites by semi-interpenetrating networks. Several important areas of polymer infiltration into fiber bundles will be researched. Preparation to towpreg for textile preform weaving and braiding and for automated tow placement is a major goal, as are the continued development of prepregging technology and the various aspects of composite part fabrication.

  2. Investigation of the relations between resin and advanced composite mechanical properties. Volume 2: Appendices

    NASA Technical Reports Server (NTRS)

    Zimmerman, R. S.; Adams, D. F.; Walrath, D. E.

    1984-01-01

    One untoughened epoxy baseline resin and three toughened epoxy resin systems were evaluated. The Hercules 3502, 2220-1, and 2220-3, and Ciba-Geigy Fibredux 914 resin systems were supplied in the uncured state by NASA-Langley and cast into thin flat specimens and round dogbone specimens. Tensile and torsional shear measurements were performed at three temperatures and two moisture conditions. Coefficients of thermal expansion and moisture expansion were also measured. Extensive scanning electron microscopic examination of fracture surfaces was performed to permit the correlation of observed failure modes with the environmental conditions under which the various specimens were tested. A micromechanics analysis was used to predict the unidirectional composite response under the various test conditions, incorporating the neat resin experimental results as the required input data. The mechanical and physical test results, the scanning electron microscope observations, and the analytical predictions were then correlated.

  3. Investigation of the relations between neat resin and advanced composite mechanical properties. Volume 1: Results

    NASA Technical Reports Server (NTRS)

    Zimmerman, R. S.; Adams, D. F.; Walrath, D. E.

    1984-01-01

    A detailed evaluation of one untoughened epoxy baseline resin and three toughened epoxy resin systems was performed. The Hercules 3502, 2220-1, and 2220-3, and Ciba-Geigy Fibredux 914 resin systems were supplied in the uncured state by NASA-Langley and cast into thin flat specimens and round dogbone specimens. Tensile and torsional shear measurements were performed at three temperatures and two moisture conditions. Coefficients of thermal expansion and moisture expansion were also measured. Extensive scanning electron microscopic examination of fracture surfaces was performed, to permit the correlation of observed failure modes with the environmental conditions under which the various specimens were tested. A micromechanics analysis was used to predict the unidirectional composite response under the various test conditions, using the neat resin experimental results as the required input data. Mechanical and physical test results, the scanning electron microscope observations, and the analytical predictions were then correlated.

  4. Free volumes and gas transport in polymers: amine-modified epoxy resins as a case study.

    PubMed

    Patil, Pushkar N; Roilo, David; Brusa, Roberto S; Miotello, Antonio; Aghion, Stefano; Ferragut, Rafael; Checchetto, Riccardo

    2016-02-01

    The CO2 transport process was studied in a series of amine-modified epoxy resins having different cross-linking densities but the same chemical environment for the penetrant molecules. Positron Annihilation Lifetime Spectroscopy (PALS) was used to monitor the free volume structure of the samples and experimentally evaluate their fractional free volume fh(T) and its temperature evolution. The analysis of the free volume hole size distribution showed that all the holes have a size large enough to accommodate the penetrant molecules at temperatures T above the glass transition temperature Tg. The measured gas diffusion constants at T > Tg have been reproduced in the framework of the free volume theory of diffusion using a novel procedure based on the use of fh(T) as an input experimental parameter. PMID:26762568

  5. Design and development of advanced adaptive polymer lenses

    NASA Astrophysics Data System (ADS)

    Santiago, Freddie

    The dissertation presented here describes advancements made in adaptive polymer lens design and implementation. Singlets and doublets lenses were constructed for visible, short- wavelength infrared (SWIR), and middle-wavelength infrared (MWIR) applications. The lenses are implemented in a variety of tactical imaging systems to demonstrate their performance. A process was developed that defines the allowable fabrication variables, first for APL singlets and then for APL doublets. A first-order finite element model is described that enables going from an optical design to APL fabrication. This model was then extended to the design of fluidic doublets, which are equivalent to their two-element glass counter-parts. Two constant volume fluidic chambers were enclosed by three flexible membranes resulting in a variable focal length doublet. Chromatic focal shift was then used to compare numerical modeling to experimentally measured results. These same tools, methodology, and process were lastly used in the definition and fabrication of the SWIR and MWIR adaptive polymer lens for tactical systems. Imaging and illumination systems are presented, based on these lensesnotably an adaptive zoom imaging system, in the MWIR. This is the first known instance of such a system in this band.

  6. [INVITED] New advances in polymer fiber Bragg gratings

    NASA Astrophysics Data System (ADS)

    Nogueira, Rogério; Oliveira, Ricardo; Bilro, Lúcia; Heidarialamdarloo, Jamshid

    2016-04-01

    During the last years, fiber Bragg gratings (FBGs) written in polymer optical fibers (POFs) have been pointed as an interesting alternative to silica FBGs for applications in sensors and in optical access networks. In order to use such components in real applications, the manipulation of POFs, as well as the increase of quality in the production of FBGs has to be achieved. In this article some of the recent advances regarding these two aspects are reported and include recent developments to produce smooth POFs end face with high quality, benefiting the current splicing process and the inscription of high quality FBGs in a few seconds. Furthermore, additional characterizations to strain, temperature, pressure, and humidity are also shown.

  7. Polymer radiation curing: polyester resins. January 1970-December 1988 (Citations from the US Patent data base). Report for January 1970-December 1988

    SciTech Connect

    Not Available

    1989-01-01

    This bibliography contains citations of selected patents concerning the processes and formulations sensitive to radiation curing in polyester resins. Electron-beam and ultraviolet radiation are emphasized. Polymer crosslinking by such electromagnetic wave radiation as in the visible wavelength is also included. Applications in paints, coatings, lacquers, printing inks, laminates, photoresists, and other substrates are discussed. (Contains 166 citations fully indexed and including a title list.)

  8. Fire retardancy enhancement of unsaturated polyester polymer resin filled with nano and micro particulate oxide additives

    NASA Astrophysics Data System (ADS)

    Ribeiro, M. C. S.; Sousa, S. P. B.; Nóvoa, P. R. O.; Pereira, C. M.; Ferreira, A. J. M.

    2014-06-01

    In the last years the traditional construction materials, such as wood, glass and steel, have been increasingly replaced by polymer composite materials due to their superior properties. However, this feature has also raised buildings' combustibility fire hazards. Polymer modification with inorganic nanoparticles can be a potential and efficient solution to control matrix flammability without sacrificing other important properties. In this study a new type of unsaturated polyester based composite materials with enhanced fire retardancy are developed, through polymer modification with nano/micro oxide particles and common flame retardants systems. For this purpose, the design of experiments based on Taguchi methodology and analyses of variance were applied. Samples with different material contents and processing parameters resultant from the L9 Taguchi orthogonal array were produced, and their fire properties assessed and quantified by single-flame source and vertical flammability tests. It was found that material and processing parameters have different effects on different properties. Unsaturated polyester composites modified with nano and micro oxide particles showed better fire performance compared to the neat composite improving at least one fire property whatever the nature of the filler. More thorough studies are required in order to improve mix design formulations towards further fire retardancy enhancement.

  9. Polymer infiltration studies

    NASA Technical Reports Server (NTRS)

    Marchello, Joseph M.

    1992-01-01

    Progress was made in several areas on the preparation of carbon fiber composites using advanced polymer resins. Polymer infiltration studies dealt with ways of preparing composite materials from advanced polymer resins and carbon fibers. This effort is comprised of an integrated approach to the process of composite part fabrication. The goal is to produce advanced composite materials for automated part fabrication using textile and robotics technology in the manufacture of subsonic and supersonic aircraft. The object is achieved through investigations at the NASA Langley Research Center and by stimulating technology transfer between contract researchers and the aircraft industry. Covered here are literature reviews, a status report on individual projects, current and planned research, publications, and scheduled technical presentations.

  10. Structure-to-property Relationships in Addition Cured Polymers 2: Resin Tg Composite Initial Mechanical Properties of Norbornenyl Cured Polyimide Resins

    NASA Technical Reports Server (NTRS)

    Alston, W. B.

    1986-01-01

    PRM (polymerization of monomeric reactants) methodology was used to prepare thirty different polyimide oligomeric resins. Monomeric composition as well as chain length between sites of crosslinks were varied to examine their effects on glass transition temperature (Tg) of the cured/postcured resins. An almost linear correlation of Tg versus molecular distance between the crosslinks was observed. An attempt was made to correlate Tg with initial mechanical properties (flexural strength and interlaminar shear strength) of unidirectional graphite fiber composites prepared with these resins. However, the scatter in mechanical strength data prevented obtaining as clear a correlation as was observed for the structural modification/crosslink distance versus Tg. Instead, only a range of composite mechanical properties was obtained at the test temperatures studied (room temperature, 288 and 316 C). Perhaps more importantly, what did become apparent during the attempted correlation study was: (1) that PMR methodology could be used to prepare composites from resins that contain a wide variety of monomer modifications, and (2) that these composites almost invariably provided satisfactory initial mechanical properties as long as the resins selected were melt processable.

  11. 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

  12. Recent advances in the development of composites based on the NCNS resins. [addition polymerized polyaromatic melamines

    NASA Technical Reports Server (NTRS)

    Kray, R. J.

    1976-01-01

    The NCNS resins, a new class of addition polymerized polyaromatic melamines, have undergone further development in the past year. Pilot plant quantities of resin NCNS-12M have been made available for evaluation. High solids laminating varnishes were prepared in alcohol/ethyl acetate and alcohol/chlorinated solvent mixtures. The prepregs had sufficient room temperature stability after three month storage to retain good processing characteristics and good bonded mechanical properties. Laminates were fabricated by vacuum bag-autoclave processing and by 5 minute press molding cycles. These laminates had low flame spread and low smoke emitting properties and retained good elevated temperature properties upon long-term oxidative aging. Humidity aging studies were carried out for 30 days at 95% R.H., 120 F. on NCNS/graphite fiber laminates. Initial results indicate that the NCNS resins, particularly those prepared from polymethylene polyphenylamines, are resistant to environmental degradation of elevated temperature mechanical strength.

  13. Improved Adhesion of Gold Thin Films Evaporated on Polymer Resin: Applications for Sensing Surfaces and MEMS

    PubMed Central

    Moazzez, Behrang; O'Brien, Stacey M.; Merschrod S., Erika F.

    2013-01-01

    We present and analyze a method to improve the morphology and mechanical properties of gold thin films for use in optical sensors or other settings where good adhesion of gold to a substrate is of importance and where controlled topography/roughness is key. To improve the adhesion of thermally evaporated gold thin films, we introduce a gold deposition step on SU-8 photoresist prior to UV exposure but after the pre-bake step of SU-8 processing. Shrinkage and distribution of residual stresses, which occur during cross-linking of the SU-8 polymer layer in the post-exposure baking step, are responsible for the higher adhesion of the top gold film to the post-deposition cured SU-8 sublayer. The SU-8 underlayer can also be used to tune the resulting gold film morphology. Our promoter-free protocol is easily integrated with existing sensor microfabrication processes. PMID:23760086

  14. A study of the kinetic, dielectric, and rheological properties of thermosetting resins used in pultruded polymer composites

    NASA Astrophysics Data System (ADS)

    Shanku, Reshma

    A comprehensive analysis has been conducted of the curing behavior of AOC VIBRINRTM E-606-6 (medium reactivity isophthalic), E-964 (high reactivity isophthalic), and P-341 (highest reactivity) polyester resins, and Shell EPON 9310 resin/EPON 9360 curing agent/EPON 537 accelerator resin system using calorimetric, dielectric, and rheological methods. The unsaturated polyester resins were cured with two different catalysts at three levels of concentration. Calorimetry and dielectrometry were employed to obtain polyester resin curing properties for the resin formulations studied. Rheological characterization of selected polyester resin formulations and the EPON 9310 resin system were also conducted. Kinetic parameters for all resin formulations were determined using a differential scanning calorimeter (DSC) by dynamic and isothermal methods. The dynamic and isothermal kinetic parameters obtained were used to generate heat flow values which were compared to the experimental DSC heat flow recorded; kinetic parameters that accurately modeled the pultrusion process were selected. The kinetic parameters were used in a numerical model to predict temperatures and degrees of cure under pultrusion processing conditions. The results obtained from the in-situ dielectric tests conducted on the pultruder in the Composites Material Laboratory at the University of Mississippi were compared to the degree of cure predictions from the numerical model and the experimental degree of cure from calorimetric analysis. Prior to the in-situ pultrusion studies, small quantities of resin formulations were tested for their dielectric cure properties when heated in an oven simulating pultrusion processing temperatures and rate of heating. This technique allowed small quantities of resins to be tested for degrees of cure. It was determined that such screening tests can be effectively conducted and can aid in pultrusion process planning. Complex viscosity profiles until gelation were generated for

  15. Fabrication and physical testing of graphite composite panels utilizing woven graphite fabric with current and advanced state-of-the-art resin systems

    NASA Technical Reports Server (NTRS)

    Lee, S. C. S.

    1979-01-01

    Three weaves were evaluated; a balanced plain weave, a balanced 8-harness satin weave, and a semiunidirectional crowfoot satin weave. The current state-of-the-art resin system selected was Fiberite's 934 Epoxy; the advanced resin systems evaluated were Phenolic, Phenolic/Novolac, Benzyl and Bismaleimide. The panels were fabricated for testing on NASA/Ames Research Center's Composites Modification Program. Room temperature mechanical tests only were performed by Hitco; the results are presented.

  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. Recyclable epoxy resins: An example of green approach for advanced composite applications

    NASA Astrophysics Data System (ADS)

    Cicala, Gianluca; Rosa, Daniela La; Musarra, Marco; Saccullo, Giuseppe; Banatao, Rey; Pastine, Stefan

    2016-05-01

    Automotive composite applications are increasingly growing due to demand for lightweight structures to comply to the requirements for fuel reduction. HP-RTM is gaining relevance as one of the preferred production technologies for high volume applications. The BMW i3 life module being a notable example of HP-RTM application. The key aspects of HP-RTM are the short injection times (i.e. less than 1min) and the fast curing of the thermoset resins (i.e. less than 10min). The choice of using thermosets poses relevant issues for their limited recycling options. The standard recycling solution is the incineration but, this solution poses some concerns in terms of global environmental impact. Novel solutions are presented in this work based on the use of recyclable epoxy systems. In our work the results of experimentation carried out by our group with cleavable ammines by Connora Technologies and bioepoxy resins by Entropy Resins will be discussed. The multiple uses of recycled matrices obtained treating the recyclable epoxy resins are discussed in the framework of a "cradle" to "crave" approach. Finally, Life Cycle Assessment (LCA) is used to evaluate the environmental benefits of the proposed approach.

  18. Polymers as advanced materials for desiccant applications, 1988

    SciTech Connect

    Czanderna, A.W.; Neidlinger, H.H.

    1990-09-01

    This report documents work to identify a next-generation, low-cost material with which solar energy or heat from another low-cost energy source can be used for regenerating the water vapor sorption activity of the desiccant. The objective of the work is to determine how the desired sorption performance of advanced desiccant materials can be predicted by understanding the role of the material modifications and material surfaces. The work concentrates on solid materials to be used for desiccant cooling systems and which process water vapor in an atmosphere to produce cooling. The work involved preparing modifications of polystyrene sulfonic acid sodium salt, synthesizing a hydrogel, and evaluating the sorption performances of these and similar commercially available polymeric materials; all materials were studied for their potential application in solid commercial desiccant cooling systems. Background information is also provided on desiccant cooling systems and the role of a desiccant material within such a system, and it includes the use of polymers as desiccant materials. 31 refs., 16 figs., 5 tabs.

  19. The effect of acrylic latex-based polymer on cow blood adhesive resins for wood composites

    NASA Astrophysics Data System (ADS)

    Yan, J.; Lin, H. L.; Feng, G. Z.; Gunasekaran, S.

    2016-07-01

    In this paper, alkali-modified cow blood adhesive (BA) and blood adhesive/acrylic latex-based adhesive (BA/ALB) were prepared. The physicochemical and adhesion properties of cow blood adhesive such as UV- visible spectra, particle size, viscosity were evaluated; share strength, water resistance were tested. UV- visible spectra indicates that the strong bonding strength of BA/ALB appeared after incorporating; the particle size of adhesive decreased with the increase of ALB concentration, by mixing ALB and BA, hydrophilic polymer tends locate or extand the protein chains and provide stability of the particles; viscosity decreased as shear rate increased in concordance with a pseudoplastic behavior; both at dry and soak conditions, BA and ALB/BA show significant difference changes when mass fraction of ALB in blend adhesive was over 30% (p < 0.05). ALB/ BA (ALB30%) is not significant different than that of phenol formaldehyde which was used as control. A combination of cow blood and acrylic latex-based adhesive significantly increased the strength and water resistance of the resulting wood.

  20. Recent Advances in Glycerol Polymers: Chemistry and Biomedical Applications

    PubMed Central

    Zhang, Heng

    2015-01-01

    Glycerol polymers are attracting increased attention due to the diversity of polymer compositions and architectures available. This article provides a brief chronological review on the current status of these polymers along with representative examples of their use for biomedical applications. First, we describe the underlying chemistry of glycerol, which provides access to a range of monomers for subsequent polymerizations. We then review the various synthetic methodologies to prepare glycerol-based polymers including polyethers, polycarbonates, polyesters, and so forth. Next, we describe several biomedical applications where glycerol polymers are being investigated including carriers for drug delivery, sealants or coatings for tissue repair, and agents possessing antibacterial activity. Fourth, we describe the growing market opportunity for the use of polymers in medicine. Finally we conclude and summarize the findings, as well as discuss potential opportunities for continued research efforts. PMID:25308354

  1. Nondestructive Evaluation of Advanced Fiber Reinforced Polymer Matrix Composites: A Technology Assessment

    NASA Technical Reports Server (NTRS)

    Yolken, H. Thomas; Matzkanin, George A.

    2009-01-01

    Because of their increasing utilization in structural applications, the nondestructive evaluation (NDE) of advanced fiber reinforced polymer composites continues to receive considerable research and development attention. Due to the heterogeneous nature of composites, the form of defects is often very different from a metal and fracture mechanisms are more complex. The purpose of this report is to provide an overview and technology assessment of the current state-of-the-art with respect to NDE of advanced fiber reinforced polymer composites.

  2. Vinyl polymer agglomerate based transition metal cation chelating ion-exchange resin containing the 8-hydroxyquinoline functional group

    SciTech Connect

    Landing, W.M.; Haraldsson, C.; Paxeus, N.

    1986-12-01

    A simple synthetic route has been developed for the immobilization of 8-hydroxyquinoline onto Fractogel TSK, a highly porous, mechanically and chemically stable, hydrophilic organic resin gel. The product exhibits an exchange capacity comparable to the highest values reported for silica-immobilized 8-hydroxyquinoline but is more stable at high pH. The resin's selectivity and efficiency of collection of cationic metal species from freshwater and seawater were investigated. The resin was used in a column sequence to obtain concentration and speciation data for Al, Mn, Fe, Co, Cu, Zn, and Cd in an organic-rich freshwater sample.

  3. Polymer infiltration studies

    NASA Technical Reports Server (NTRS)

    Marchello, Joseph M.

    1995-01-01

    Polymer infiltration investigations were directed toward development of methods by which to produce advanced composite material for automated part fabrication utilizing textile and robotic technology in the manufacture of subsonic and supersonic aircraft. Significant progress was made during the project on the preparation of carbon fiber composites using advanced polymer resins. The findings and results of the project are summarized in the attached paper entitled 'Powder-Coated Towpreg: Avenues to Near Net Shape Fabrication of High Performance Composite.' Also attached to this report is the second of two patent applications submitted as a result of these studies.

  4. Radioembolization using 90Y-resin microspheres for patients with advanced hepatocellular carcinoma

    SciTech Connect

    Sangro, Bruno . E-mail: bsangro@unav.es; Bilbao, Jose I.; Boan, Jose; Martinez-Cuesta, Antonio; Benito, Alberto; Rodriguez, Javier; Panizo, Angel; Gil, Belen; Inarrairaegui, Mercedes; Herrero, Ignacio; Quiroga, Jorge; Prieto, Jesus

    2006-11-01

    Purpose: To investigate the antitumor effect of resin microspheres loaded with 90-yttrium against hepatocellular carcinoma and their safety in the setting of liver cirrhosis. Patients and Methods: Data from 24 consecutive patients with hepatocellular carcinoma (HCC) treated by radioembolization in the period from September 2003 to February 2005 were reviewed. Patients received no further antineoplastic therapy. A comprehensive evaluation was performed to prevent the risk of damage due to microsphere misplacing. Patients were discharged the day after microspheres injection. Results: Serious liver toxicity observed among cirrhotic patients in a first period was subsequently prevented by modifying the selection criteria and the method for calculating the activity to be administered. Among 21 patients evaluable for response using Response Evaluation Criteria in Solid Tumors (RECIST) criteria, a reduction in size of target lesions was observed in all but 1 patient. When considering only target lesions, disease control rate and response rate were 100% and 23.8%, respectively. However, 43% of patients progressed in the liver in the form of new lesions appearing a median time of 3 months after radioembolization. Conclusion: Our experience in these series of patients indicates that radioembolization using resin microspheres has a significant antitumor effect against HCC and that using stringent selection criteria and conservative models for calculating Radiation activity to be administered, radioembolization can be performed safely even in cirrhotic patients.

  5. New Advanced Materials for High Performance at the Resin-Dentine Interface.

    PubMed

    Toledano, Manuel; Osorio, Raquel

    2015-01-01

    This chapter provides a tool for the integration of new concepts and biomaterials related with the resin-dentine interface. The principles of dentine demineralisation and remineralisation that shape modern restorative dentistry practices, as well as considerations for the selection of new materials for different restorative approaches, are emphasised. Re-incorporation of mineral into the demineralised dentine matrix is important since the mineral precipitated may work as a constant site for further nucleation, and the remineralised subsurface of the tissue may be more resistant to subsequent acid attack. This deposition of minerals may be due to both spontaneous precipitation induced by local supersaturation of Ca and P in the presence of non-specific tissue alkaline phosphatase or through heterogeneous nucleation sites provided by phosphoproteins within the dentine collagen matrix. Nucleation is a multistep process involving both protein and mineral transition and suggests a temporally synchronised process. Dentine provides both structural and chemical frameworks, acting as a scaffold for mineral deposition at specific sites. The ultimate goal in the design and improvement of new materials for high performance at the resin-dentine interface is to render a stronger and durable adhesion to dental tissues despite the severe conditions in the oral environment. In the present chapter, glass ionomers, calcium-phosphate cements and doped dental adhesives have been selected to represent the cutting edge biomaterials at the interface. PMID:26201275

  6. Recent advances in research on carbon nanotube-polymer composites.

    PubMed

    Byrne, Michele T; Gun'ko, Yurii K

    2010-04-18

    Carbon nanotubes (CNTs) demonstrate remarkable electrical, thermal, and mechanical properties, which allow a number of exciting potential applications. In this article, we review the most recent progress in research on the development of CNT-polymer composites, with particular attention to their mechanical and electrical (conductive) properties. Various functionalization and fabrication approaches and their role in the preparation of CNT-polymer composites with improved mechanical and electrical properties are discussed. We tabulate the most recent values of Young's modulus and electrical conductivities for various CNT-polymer composites and compare the effectiveness of different processing techniques. Finally, we give a future outlook for the development of CNT-polymer composites as potential alternative materials for various applications, including flexible electrodes in displays, electronic paper, antistatic coatings, bullet-proof vests, protective clothing, and high-performance composites for aircraft and automotive industries. PMID:20496401

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

    Code of Federal Regulations, 2014 CFR

    2014-07-01

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

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

    Code of Federal Regulations, 2011 CFR

    2011-07-01

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

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

    Code of Federal Regulations, 2010 CFR

    2010-07-01

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

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

    Code of Federal Regulations, 2012 CFR

    2012-07-01

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

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

    Code of Federal Regulations, 2013 CFR

    2013-07-01

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

  12. Advanced Proton Conducting Polymer Electrolytes for Electrochemical Capacitors

    NASA Astrophysics Data System (ADS)

    Gao, Han

    Research on solid electrochemical energy storage devices aims to provide high performance, low cost, and safe operation solutions for emerging applications from flexible consumer electronics to microelectronics. Polymer electrolytes, minimizing device sealing and liquid electrolyte leakage, are key enablers for these next-generation technologies. In this thesis, a novel proton-conducing polymer electrolyte system has been developed using heteropolyacids (HPAs) and polyvinyl alcohol for electrochemical capacitors. A thorough understanding of proton conduction mechanisms of HPAs together with the interactions among HPAs, additives, and polymer framework has been developed. Structure and chemical bonding of the electrolytes have been studied extensively to identify and elucidate key attributes affecting the electrolyte properties. Numerical models describing the proton conduction mechanism have been applied to differentiate those attributes. The performance optimization of the polymer electrolytes through additives, polymer structural modifications, and synthesis of alternative HPAs has achieved several important milestones, including: (a) high proton mobility and proton density; (b) good ion accessibility at electrode/electrolyte interface; (c) wide electrochemical stability window; and (d) good environmental stability. Specifically, high proton mobility has been addressed by cross-linking the polymer framework to improve the water storage capability at normal-to-high humidity conditions (e.g. 50-80% RH) as well as by incorporating nano-fillers to enhance the water retention at normal humidity levels (e.g. 30-60% RH). High proton density has been reached by utilizing additional proton donors (i.e. acidic plasticizers) and by developing different HPAs. Good ion accessibility has been achieved through addition of plasticizers. Electrochemical stability window of the electrolyte system has also been investigated and expanded by utilizing HPAs with different heteroatoms

  13. Basic failure mechanisms in advanced composites. [composed of epoxy resins reinforced with carbon fibers

    NASA Technical Reports Server (NTRS)

    Mazzio, V. F.; Mehan, R. L.; Mullin, J. V.

    1973-01-01

    The fundamental failure mechanisms which result from the interaction of thermal cycling and mechanical loading of carbon-epoxy composites were studied. This work was confined to epoxy resin uniderictionally reinforced with HTS carbon fibers, and consists of first identifying local fiber, matrix and interface failure mechanisms using the model composite specimen containing a small number of fibers so that optical techniques can be used for characterization. After the local fracture process has been established for both mechanical loading and thermal cycling, engineering composite properties and gross fracture modes are then examined to determine how the local events contribute to real composite performance. Flexural strength in high fiber content specimens shows an increase in strength with increased thermal cycling. Similar behavior is noted for 25 v/o material up to 200 cycles; however, there is a drastic reduction after 200 cycles indicating a major loss of integrity probably through the accumulation of local cleavage cracks in the tensile region.

  14. Advanced zinc-doped adhesives for high performance at the resin-carious dentin interface.

    PubMed

    Toledano, Manuel; Osorio, Raquel; Osorio, Estrella; García-Godoy, Franklin; Toledano-Osorio, Manuel; Aguilera, Fátima S

    2016-09-01

    The purpose of this study was to evaluate the remineralization ability of an etch-and-rinse Zn-doped resin applied on caries-affected dentin (CAD). CAD surfaces were subjected to: (i) 37% phosphoric acid (PA) or (ii) 0.5M ethylenediaminetetraacetic acid (EDTA). 10wt% ZnO nanoparticles or 2wt% ZnCl2 were added into the adhesive Single Bond (SB), to create the following groups: PA+SB, PA+SB-ZnO, PA+SB-ZnCl2, EDTA+SB, EDTA+SB-ZnO, EDTA+SB-ZnCl2. Bonded interfaces were submitted to mechanical loading or stored during 24h. Remineralization of the bonded interfaces was studied by AFM nano-indentation (hardness and Young׳s modulus), Raman spectroscopy [mapping with principal component analysis (PCA), and hierarchical cluster analysis (HCA)] and Masson׳s trichrome staining technique. Dentin samples treated with PA+SB-ZnO attained the highest values of nano-mechanical properties. Load cycling increased both mineralization and crystallographic maturity at the interface; this effect was specially noticed when using ZnCl2-doped resin in EDTA-treated carious dentin. Crosslinking attained higher frequencies indicating better conformation and organization of collagen in specimens treated with PA+SB-ZnO, after load cycling. Trichrome staining technique depicted a deeper demineralized dentin fringe that became reduced after loading, and it was not observable in EDTA+SB groups. Multivariate analysis confirmed de homogenizing effect of load cycling in the percentage of variances, traces of centroids and distribution of clusters, especially in specimens treated with EDTA+SB-ZnCl2. PMID:27232828

  15. Do Membranes Dream of Electric Tubes? Advanced Membranes Using Carbon Nanotube - Polymer Nanocomposites

    NASA Astrophysics Data System (ADS)

    de Lannoy, Charles-Francois Pedro Claude Karolek Ghislain

    Membrane technologies represent an energy efficient, effective solution for treating municipal and commercial waters/wastewaters. Membranes are predominantly polymer-based and despite steady advances in polymeric materials, they continue to suffer from operational problems including biofouling and breakages. This work addresses these two disparate problems by developing novel CNT-polymer nanocomposite materials that contain variously functionalized carbon nanotubes (fCNTs) in low quantities (<0.5wt%). Several strategies have been employed to achieve highly functional CNT-polymer nanocomposite membranes including blend mixing, ionic charge association, and covalent cross-linking with monomer and oligomer constituents. These CNT-polymer nanocomposite membranes were compared to traditional polymer membranes across various properties including increased Young's Modulus, changes in surface hydrophilicity, fine control over molecular weight cut-off and flux, and surface electrical conductivity. Membranes with high surface electrical conductivity were further tested for their anti-biofouling properties. Finally, CNT stability and polymer compatibility were evaluated throughout membrane manufacture, use, and cleaning. The incorporation of CNTs mixed in bulk phase and linked through ionic associations in polymer matrices showed significant (50%) increases in Young's modulus for certain CNT functionalizations and derivatization percent. Membranes formed with high surface electrical conductivity demonstrated almost complete resistance to biofouling (> 95%) in long-term bacterially challenged experiments. CNTs and polymer mixtures that lacked covalent or ionic bonds were susceptible to significant (up to 10%) loss of CNTs during membrane non-solvent gelation and aggressive chemical cleaning treatment. Functionalized carbon nanotubes endow polymer membranes with their unique strength and electrically conductive properties. These added properties were demonstrated to greatly

  16. Recent advances in the chemical modification of unsaturated polymers

    NASA Technical Reports Server (NTRS)

    Schulz, D. N.; Turner, S. R.; Golub, M. A.

    1982-01-01

    The present discussion has the objective to update the most comprehensive reviews on the considered subject and to fill in the gaps of less complete, but more modern treatments. Only simple chemical functionalization or structural modification of unsaturated polymers are covered, and the literature of diene polymer modification since 1974 is emphasized. Attention is given to hydrogenation, halogenation and hydrohalogenation, cyclization, cis-trans isomerization, epoxidation, ene and other cycloaddition reactions, sulfonation, carboxylation, phosphonylation, sulfenyl chloride addition, carbene addition, metalation, and silylation. It is pointed out that modern synthetic reagents and catalysts have been advantageously employed to improve process and/or product quality. Synthetic techniques have been refined to allow the selective modification of specific polymer microstructures or blocks.

  17. Manufacturing Aspects of Advanced Polymer Composites for Automotive Applications

    NASA Astrophysics Data System (ADS)

    Friedrich, Klaus; Almajid, Abdulhakim A.

    2013-04-01

    Composite materials, in most cases fiber reinforced polymers, are nowadays used in many applications in which light weight and high specific modulus and strength are critical issues. The constituents of these materials and their special advantages relative to traditional materials are described in this paper. Further details are outlined regarding the present markets of polymer composites in Europe, and their special application in the automotive industry. In particular, the manufacturing of parts from thermoplastic as well as thermosetting, short and continuous fiber reinforced composites is emphasized.

  18. Gamma irradiation-induced modifications of polymers found in nuclear waste embedding processes Part II: The ion-exchange resin

    NASA Astrophysics Data System (ADS)

    Debré, O.; Nsouli, B.; Thomas, J.-P.; Stevenson, I.; Colombini, D.; Romero, M.-A.

    1997-08-01

    Ion exchange resins (IERs) saturated in cesium and borate ions are well representative of low and medium activity nuclear waste to be embedded in an epoxy resin/amine hardener, such a conditioning procedure being under qualification. In order to test these materials in realistic conditions they are externally irradiated (air and water), in mixed beds saturated in fixed ions (cesium and borate) and water. Irradiation effects are evidenced with the HSF-SIMS technique by the variation of the emission characteristic of both the fixed ions, the chemical structure of the IERs and their interrelationship, both from the analysis of the solid material and of the residual or rinsing water. It appears that the fixed ions can be released in surrounding water as a consequence of radiation-induced resin fragments solubility.

  19. Thermoplastic polymer patterning without residual layer by advanced nanoimprinting schemes

    NASA Astrophysics Data System (ADS)

    Park, Hyunsoo; Cheng, Xing

    2009-06-01

    Nanoimprinting is a fast-growing technique for nanoscale patterning. One of the remaining issues in nanoimprinting is the removal of the residual layer after nanoimprinting. Traditionally the residual layer is removed by an oxygen reactive-ion etching (RIE) step. The need for a vacuum environment and dedicated equipment in this step lowers the throughput and increases the cost of the nanoimprinting process. It also prevents the possibility of patterning isolated functional polymers because oxygen RIE destroys the functional materials. In this work, novel nanoimprinting schemes are developed to nondestructively remove the residual layer in thermal nanoimprinting by solvent developing and dewetting. Combined with a transfer-bonding technique, three-dimensional polymer scaffolds are achieved. The techniques developed here eliminate the RIE step in thermal nanoimprinting and are compatible with roller nanoimprinting for large-scale patterning of polymer micro- or nanostructures. The technique also opens up new applications for nanoimprinting in patterning isolated conjugated polymers for organic electronic devices and circuits.

  20. Thermoplastic polymer patterning without residual layer by advanced nanoimprinting schemes.

    PubMed

    Park, Hyunsoo; Cheng, Xing

    2009-06-17

    Nanoimprinting is a fast-growing technique for nanoscale patterning. One of the remaining issues in nanoimprinting is the removal of the residual layer after nanoimprinting. Traditionally the residual layer is removed by an oxygen reactive-ion etching (RIE) step. The need for a vacuum environment and dedicated equipment in this step lowers the throughput and increases the cost of the nanoimprinting process. It also prevents the possibility of patterning isolated functional polymers because oxygen RIE destroys the functional materials. In this work, novel nanoimprinting schemes are developed to nondestructively remove the residual layer in thermal nanoimprinting by solvent developing and dewetting. Combined with a transfer-bonding technique, three-dimensional polymer scaffolds are achieved. The techniques developed here eliminate the RIE step in thermal nanoimprinting and are compatible with roller nanoimprinting for large-scale patterning of polymer micro- or nanostructures. The technique also opens up new applications for nanoimprinting in patterning isolated conjugated polymers for organic electronic devices and circuits. PMID:19468173

  1. Aromatic/aliphatic diamine derivatives for advanced compositions and polymers

    NASA Technical Reports Server (NTRS)

    Delozier, Donovan M. (Inventor); Watson, Kent A. (Inventor); Connell, John W. (Inventor); Smith, Jr., Joseph G. (Inventor)

    2010-01-01

    Novel compositions of matter comprise certain derivatives of 9,9-dialkyl fluorene diamine (AFDA). The resultant compositions, whether compositions of matter or monomers that are subsequently incorporated into a polymer, are unique and useful in a variety of applications. Useful applications of AFDA-based material include heavy ion radiation shielding components and components of optical and electronic devices.

  2. 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.

  3. Recent advances in metathesis-derived polymers containing transition metals in the side chain.

    PubMed

    Dragutan, Ileana; Dragutan, Valerian; Simionescu, Bogdan C; Demonceau, Albert; Fischer, Helmut

    2015-01-01

    This account critically surveys the field of side-chain transition metal-containing polymers as prepared by controlled living ring-opening metathesis polymerization (ROMP) of the respective metal-incorporating monomers. Ferrocene- and other metallocene-modified polymers, macromolecules including metal-carbonyl complexes, polymers tethering early or late transition metal complexes, etc. are herein discussed. Recent advances in the design and syntheses reported mainly during the last three years are highlighted, with special emphasis on new trends for superior applications of these hybrid materials. PMID:26877797

  4. Recent advances in metathesis-derived polymers containing transition metals in the side chain

    PubMed Central

    Demonceau, Albert; Fischer, Helmut

    2015-01-01

    Summary This account critically surveys the field of side-chain transition metal-containing polymers as prepared by controlled living ring-opening metathesis polymerization (ROMP) of the respective metal-incorporating monomers. Ferrocene- and other metallocene-modified polymers, macromolecules including metal-carbonyl complexes, polymers tethering early or late transition metal complexes, etc. are herein discussed. Recent advances in the design and syntheses reported mainly during the last three years are highlighted, with special emphasis on new trends for superior applications of these hybrid materials. PMID:26877797

  5. Polymer/Graphene Hybrids for Advanced Energy-Conversion and -Storage Materials.

    PubMed

    Cui, Linfan; Gao, Jian; Xu, Tong; Zhao, Yang; Qu, Liangti

    2016-04-20

    Polymer/graphene-based materials with interesting physical and chemical properties have been attracting considerable attention and have been shown to have great potential as active materials in the field of energy conversion and storage. In this review, we focus on recent significant advances in the fabrication and application of polymer/graphene hybrids as electrocatalysts and electrode materials. Synthetic strategies and application of these materials in energy conversion and storage are presented, particularly in devices such as fuel cells, actuators, and supercapacitors, accompanied with a discussion of the challenges and research directions necessary for the future development of polymer/graphene hybrids. PMID:26878997

  6. Advanced treatment of textile dyeing secondary effluent using magnetic anion exchange resin and its effect on organic fouling in subsequent RO membrane.

    PubMed

    Yang, Cheng; Li, Li; Shi, Jialu; Long, Chao; Li, Aimin

    2015-03-01

    Strict regulations are forcing dyeing factory to upgrade existing waste treatment system. In this study, advanced treatment of dyeing secondary effluent by magnetic anion exchange resin (NDMP) was investigated and compared with ultrafiltration (UF); NDMP as a pre-treatment of reverse osmosis (RO) was also studied. NDMP resin (20 mL/L) gave higher removal of dissolved organic carbon (DOC) (83.9%) and colority (94.9%) than UF with a cut-off of 10 kDa (only 48.6% and 44.1%, respectively), showing that NDMP treatment was effective to meet the stringent discharge limit of DOC and colority. Besides, NDMP resin (20 mL/L) as a pretreatment of RO increased the permeate flux by 12.5% and reduced irreversible membrane fouling by 6.6%, but UF pretreatment did not mitigate RO membrane fouling. The results of excitation-emission matrix fluorescence spectra and resin fractions showed that NDMP had more efficient removal than UF for transphilic acid and hydrophilic fraction, such as protein-like organic matters and soluble microbial products, which contributed to a significant proportion of RO membrane fouling. In sum, NDMP resin treatment not only gave effective removal of DOC and colority of dyeing secondary effluent, but exhibited some improvement for RO membrane flux and irreversible fouling. PMID:25463217

  7. Microgravity polymer and crystal growth at the Advanced Materials Center for the Commercial Development of Space

    NASA Technical Reports Server (NTRS)

    Mccauley, Lisa A.

    1990-01-01

    The microgravity research programs currently conducted by the Advanced Materials Center for the Commercial Development of Space (CCDS) are briefly reviewed. Polymer processing in space, which constitutes the most active microgravity program at the Advanced Materials CCDS, is conducted in three areas: membrane processing, multiphase composite behavior, and plasma polymerization. Current work in microgravity crystal growth is discussed with particular reference to the development of the Zeolite Crystal Growth facility.

  8. Recent Advances in Thermoplastic Puncture-Healing Polymers

    NASA Technical Reports Server (NTRS)

    Gordon, K. L.; Working, D. C.; Wise, K. E.; Bogert, P. B.; Britton, S. M.; Topping, C.C.; Smith, J. Y.; Siochi, E. J.

    2009-01-01

    Self-healing materials provide a route for enhanced damage tolerance in materials for aerospace applications. In particular, puncture-healing upon impact has the potential to mitigate significant damage caused by high velocity micrometeoroid impacts. This type of material also has the potential to improve damage tolerance in load bearing structures to enhance vehicle health and aircraft durability. The materials being studied are those capable of instantaneous puncture healing, providing a mechanism for mechanical property retention in lightweight structures. These systems have demonstrated healing capability following penetration of fast moving projectiles -- velocities that range from 9 mm bullets shot from a gun (approx.330 m/sec) to close to micrometeoroid debris velocities of 4800 m/sec. In this presentation, we report on a suite of polymeric materials possessing this characteristic. Figure 1 illustrates the puncture healing concept. Puncture healing in these materials is dependent upon how the combination of a polymer's viscoelastic properties responds to the energy input resulting from the puncture event. Projectile penetration increases the temperature in the vicinity of the impact. Self-healing behavior occurs following puncture, whereby energy must be transferred to the material during impact both elastically and inelastically, thus establishing two requirements for puncture healing to occur: a.) The need for the puncture event to produce a local melt state in the polymer material and b.) The molten material has to have sufficient melt elasticity to snap back and close the hole. 1,2 Previous ballistic testing studies revealed that Surlyn materials warmed up to a temperature approx.98 C during projectile puncture (3 C higher than it s melting temperature). 1,2 The temperature increase produces a localized flow state and the melt elasticity to snap back thus sealing the hole. Table 1 lists the commercially polymers studied here, together with their physical

  9. 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.

  10. 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.

  11. 21 CFR 172.280 - Terpene resin.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

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

  12. 21 CFR 172.280 - Terpene resin.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

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

  13. 21 CFR 172.280 - Terpene resin.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

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

  14. 21 CFR 172.280 - Terpene resin.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

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

  15. 21 CFR 172.280 - Terpene resin.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

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

  16. Recent Advances in Targeted Drug Delivery Approaches Using Dendritic Polymers

    PubMed Central

    Bugno, Jason; Hsu, Hao-Jui; Hong, Seungpyo

    2014-01-01

    Since they were first synthesized over 30 years ago, dendrimers have seen rapid translation into various biomedical applications. A number of reports have not only demonstrated their clinical utility, but also revealed novel design approaches and strategies based on the elucidation of underlying mechanisms governing their biological interactions. This review focuses on presenting the latest advances in dendrimer design, discussing the current mechanistic understandings, and highlighting recent developments and targeted approaches using dendrimers in drug/gene delivery. PMID:26221937

  17. Analytical modeling and sensor monitoring for optimal processing of advanced textile structural composites by resin transfer molding

    NASA Technical Reports Server (NTRS)

    Loos, Alfred C.; Macrae, John D.; Hammond, Vincent H.; Kranbuehl, David E.; Hart, Sean M.; Hasko, Gregory H.; Markus, Alan M.

    1993-01-01

    A two-dimensional model of the resin transfer molding (RTM) process was developed which can be used to simulate the infiltration of resin into an anisotropic fibrous preform. Frequency dependent electromagnetic sensing (FDEMS) has been developed for in situ monitoring of the RTM process. Flow visualization tests were performed to obtain data which can be used to verify the sensor measurements and the model predictions. Results of the tests showed that FDEMS can accurately detect the position of the resin flow-front during mold filling, and that the model predicted flow-front patterns agreed well with the measured flow-front patterns.

  18. Advances with polymer-free amphilimus-eluting stents.

    PubMed

    CARRIé, Didier

    2016-06-01

    Despite the improved clinical outcomes following the availability of second generation drug eluting stents (DES), percutaneous coronary intervention (PCI) is associated with worse clinical and angiographic outcomes among the patients with diabetes mellitus (DM) than among non-diabetics. The Cre8 Amphilimus-eluting DES is polymer-free, resulting in a reduced inflammatory response and lower risk of stent thrombosis. In a clinical study, it showed equivalent efficacy and safety in diabetic and non-diabetic populations, a unique finding among DES studies. These findings were confirmed in a real-world study, Investig8, and another real-world study, Particip8, is ongoing. The RESERVOIR Clinical Trial recruited patients with DM and showed noninferiority of the Cre8 DES compared to an everolimus eluting DES (EES) in the overall group but showed a statistical superiority of Cre8 in diabetic patients with higher metabolic dysfunctions. The Cre8 DES is therefore a valuable option for this important patient population. PMID:26934663

  19. Advances in ferroelectric polymers for shock compression sensors

    SciTech Connect

    Bauer, F.; Moulard, H.; Samara, G.

    1997-10-01

    Our studies of the shock compression response of PVDF polymer are continuing in order to understand the physical properties under shock loading and to develop high fidelity, reproducible, time-resolved dynamic stress gauges. New PVDF technology, new electrode configurations and piezoelectric analysis have resulted in enhanced precision gauges. Our new standard gauges have a precision of better than 1% in electric charge release under shock up to 15 GPa. The piezoelectric response of shock compressed PVDF gauges 1 mm{sup 2} in active area has been studied and yielded well-behaved reproducible data up to 20 GPa. Analysis of the response of these gauges in the {open_quotes}thin mode regime{close_quotes} using a Lagrangian hydrocode will be presented. P(VDF-TrFE) copolymers exhibit unique piezoelectric properties over a wide range of temperature depending on the composition. Their properties and phase transitions are being investigated. Emphasis of the presentation will be on key results and implications.

  20. Advances on Magnetic Nanocarriers Based on Natural Polymers.

    PubMed

    Muzzalupo, Rita; Tavano, Lorena

    2016-01-01

    The use of nanodevices to transport active compounds like small-molecular drugs, peptides, or genes found an increased attention throughout the different fields of natural sciences. Moreover, recent research trends are focused on the employment of smart nanocarriers able to react on certain internal or external applied stimuli, in order to achieve temporal and site-specific drugs/gene release. In contrast to traditional biodegradable nanocarriers that slowly release drugs inside the cells, these smart nanosystems are able to quickly release or even dump drugs in response to a specific biological signal in the target cancer cells such lower pH, high redox potential or over expression of enzymes or to external stimuli such as temperature, light, ultrasounds and magnetic field. This review gives a brief overview about some types of stimuli-responsive nanocarriers, with the main focus on magnetic fieldresponsive devices obtained from natural polymers. The concept of magnetic field-sensitive nanocarriers, their advantages and disadvantages, the methods of preparation and applications in various fields of drug delivery will be explored, giving an exhaustive collection of the findings of recent investigations. PMID:26861649

  1. Advances in ferroelectric polymers for shock compression sensors

    SciTech Connect

    Bauer, F.; Moulard, H.; Samara, G.

    1998-07-01

    Our studies of the shock compression response of PVDF polymer are continuing in order to understand the physical properties under shock loading and to develop high fidelity, reproducible, time-resolved dynamic stress gauges. New PVDF technology, new electrode configurations and piezoelectric analysis have resulted in enhanced precision gauges. Our new standard gauges have a precision of better than 1{percent} in electrical charge release under shock up to 15 GPa. The piezoelectric response of shock compressed PVDF gauges 1 mm{sup 2} in active area has been studied and yielded well-behaved reproducible data up to 20 GPa. Analysis of the response of these gauges in the {open_quotes}thin mode regime{close_quotes} using a Lagrangian hydrocode will be presented. P(VDF-TrFE) copolymers exhibit unique piezoelectric properties over a wide range of temperature depending on the composition. Their properties and phase transitions are being investigated. Emphasis of the presentation will be on key results and implications. {copyright} {ital 1998 American Institute of Physics.}

  2. Current Advances in Polymer-Based Nanotheranostics for Cancer Treatment and Diagnosis

    PubMed Central

    2015-01-01

    Nanotheranostics is a relatively new, fast-growing field that combines the advantages of treatment and diagnosis via a single nanoscale carrier. The ability to bundle both therapeutic and diagnostic capabilities into one package offers exciting prospects for the development of novel nanomedicine. Nanotheranostics can deliver treatment while simultaneously monitoring therapy response in real-time, thereby decreasing the potential of over- or under-dosing patients. Polymer-based nanomaterials, in particular, have been used extensively as carriers for both therapeutic and bioimaging agents and thus hold great promise for the construction of multifunctional theranostic formulations. Herein, we review recent advances in polymer-based systems for nanotheranostics, with a particular focus on their applications in cancer research. We summarize the use of polymer nanomaterials for drug delivery, gene delivery, and photodynamic therapy, combined with imaging agents for magnetic resonance imaging, radionuclide imaging, and fluorescence imaging. PMID:25014486

  3. Advanced polymer systems for optoelectronic integrated circuit applications

    NASA Astrophysics Data System (ADS)

    Eldada, Louay A.; Stengel, Kelly M. T.; Shacklette, Lawrence W.; Norwood, Robert A.; Xu, Chengzeng; Wu, Chengjiu; Yardley, James T.

    1997-01-01

    An advanced versatile low-cost polymeric waveguide technology is proposed for optoelectronic integrated circuit applications. We have developed high-performance organic polymeric materials that can be readily made into both multimode and single-mode optical waveguide structures of controlled numerical aperture (NA) and geometry. These materials are formed from highly crosslinked acrylate monomers with specific linkages that determine properties such as flexibility, toughness, loss, and stability against yellowing and humidity. These monomers are intermiscible, providing for precise adjustment of the refractive index from 1.30 to 1.60. Waveguides are formed photolithographically, with the liquid monomer mixture polymerizing upon illumination in the UV via either mask exposure or laser direct-writing. A wide range of rigid and flexible substrates can be used, including glass, quartz, oxidized silicon, glass-filled epoxy printed circuit board substrate, and flexible polyimide film. We discuss the use of these materials on chips and on multi-chip modules (MCMs), specifically in transceivers where we adaptively produced waveguides on vertical-cavity surface-emitting lasers (VCSELs) embedded in transmitter MCMs and on high- speed photodetector chips in receiver MCMs. Light coupling from and to chips is achieved by cutting 45 degree mirrors using excimer laser ablation. The fabrication of our polymeric structures directly on the modules provides for stability, ruggedness, and hermeticity in packaging.

  4. 'Click' functionalised polymer resins: a new approach to the synthesis of surface attached bipyridinium and naphthalene diimide [2]rotaxanes.

    PubMed

    Wilson, Hannah; Byrne, Sean; Bampos, Nick; Mullen, Kathleen M

    2013-04-01

    Herein we describe the design and synthesis of a series of solid-tethered [2]rotaxanes utilising crown ether-naphthalene diimide or crown ether-bipyridinium host guest interactions. TentaGel polystyrene resins were initially modified in a two-stage procedure to azide functionalised beads before the target supramolecular architectures were attached using a copper catalysed "click" procedure. The final assembly was examined using IR spectroscopy and gel-phase (1)H High Resolution Magic Angle Spinning (HR MAS) NMR spectroscopy. The HR MAS technique enabled a direct comparison between the solid-tethered architectures and the synthesis and characterisation of analogous solution-based [2]rotaxanes to be made. PMID:23380978

  5. Development of critical molecular weight-property specifications for high performance polymers used as adhesives and composites

    NASA Technical Reports Server (NTRS)

    Kranbuehl, D. E.

    1982-01-01

    The polyimide resin, LARC-160, was prepared from diethyl-3, 3', 4,4'-benzophenone tetracarboxylate, ethyl-5-norbornene-2,3-dicarboxylate and Jeffamine AP-22. The imidization reactions of NE and BTDE were studied by HPLC, C-13-NMR and IR. NE imidizes slowly at 12 C; BTDE imidizes when the resin is heated above 100 C. Both imidization reactions proceed directly to the imide. Neither amic acid is present in significant quantities at any stage of the imidization reactions. The monomer mixture was stored at 12 C for periods up to 14 months. The effects of resin aging at this temperature on the chemical composition of the resin monomer mixture and the imidized polymer formed on curing were investigated. Aging the resin monomer mixture has the effect of partially advancing the imidization reaction. The average size of the cured polymer increases slightly with resin age.

  6. Mechanically stiff, electrically conductive composites of polymers and carbon nanotubes

    DOEpatents

    Worsley, Marcus A.; Kucheyev, Sergei O.; Baumann, Theodore F.; Kuntz, Joshua D.; Satcher, Jr., Joe H.; Hamza, Alex V.

    2015-07-21

    Using SWNT-CA as scaffolds to fabricate stiff, highly conductive polymer (PDMS) composites. The SWNT-CA is immersing in a polymer resin to produce a SWNT-CA infiltrated with a polymer resin. The SWNT-CA infiltrated with a polymer resin is cured to produce the stiff and electrically conductive composite of carbon nanotube aerogel and polymer.

  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. The NASA "PERS" Program: Solid Polymer Electrolyte Development for Advanced Lithium-Based Batteries

    NASA Technical Reports Server (NTRS)

    Baldwin, Richard S.; Bennett, William R.

    2007-01-01

    In fiscal year 2000, The National Aeronautics and Space Administration (NASA) and the Air Force Research Laboratory (AFRL) established a collaborative effort to support the development of polymer-based, lithium-based cell chemistries and battery technologies to address the next generation of aerospace applications and mission needs. The ultimate objective of this development program, which was referred to as the Polymer Energy Rechargeable System (PERS), was to establish a world-class technology capability and U.S. leadership in polymer-based battery technology for aerospace applications. Programmatically, the PERS initiative exploited both interagency collaborations to address common technology and engineering issues and the active participation of academia and private industry. The initial program phases focused on R&D activities to address the critical technical issues and challenges at the cell level. Out of a total of 38 proposals received in response to a NASA Research Announcement (NRA) solicitation, 18 proposals (13 contracts and 5 grants) were selected for initial award to address these technical challenges. Brief summaries of technical approaches, results and accomplishments of the PERS Program development efforts are presented. With Agency support provided through FY 2004, the PERS Program efforts were concluded in 2005, as internal reorganizations and funding cuts resulted in shifting programmatic priorities within NASA. Technically, the PERS Program participants explored, to various degrees over the lifetime of the formal program, a variety of conceptual approaches for developing and demonstrating performance of a viable advanced solid polymer electrolyte possessing the desired attributes, as well as several participants addressing all components of an integrated cell configuration. Programmatically, the NASA PERS Program was very successful, even though the very challenging technical goals for achieving a viable solid polymer electrolyte material or

  9. Polymer/inorganic nanocomposites with tailored hierarchical structure as advanced dielectric materials

    SciTech Connect

    Manias, Evangelos; Randall, Clive; Tomer, Vivek; Polyzos, Georgios

    2012-01-01

    Most advances and commercial successes of polymer/inorganic nanocomposites rely only on the dispersion of nanoparticles in a polymer matrix. Such approaches leave untapped opportunities where performance can be improved by controlling the larger length-scale structures. Here, we review selected examples where the hierarchical structure (from millimeter to nanometer) is tailored to control the transport properties of the materials, giving rise to marked property enhancements, relevant to dielectric materials for power capacitors. These examples address composite structures that are self-assembled, both at the nm and the micron scales, and, thus, can be produced using standard industrial practices. Specifically, polyethylene (PE) blends or poly(vinylidene fluoride) (PVDF) copolymers are reinforced with nanofillers; these composites are designed with high filler orientation, which yielded marked improvements in electric-field breakdown strength and, consequently, large improvements in their recoverable energy densities.

  10. High Thermal Conductivity Polymer Matrix Composites (PMC) for Advanced Space Radiators

    NASA Technical Reports Server (NTRS)

    Shin, E. Eugene; Bowman, Cheryl; Beach, Duane

    2007-01-01

    High temperature polymer matrix composites (PMC) reinforced with high thermal conductivity (approx. 1000 W/mK) pitch-based carbon fibers are evaluated for a facesheet/fin structure of large space radiator systems. Significant weight reductions along with improved thermal performance, structural integrity and space durability toward its metallic counterparts were envisioned. Candidate commercial resin systems including Cyanate Esters, BMIs, and polyimide were selected based on thermal capabilities and processability. PMC laminates were designed to match the thermal expansion coefficient of various metal heat pipes or tubes. Large, but thin composite panels were successfully fabricated after optimizing cure conditions. Space durability of PMC with potential degradation mechanisms was assessed by simulated thermal aging tests in high vacuum, 1-3 x 10(exp -6) torr, at three temperatures, 227 C, 277 C, and 316 C for up to one year. Nanocomposites with vapor-grown carbon nano-fibers and exfoliated graphite flakes were attempted to improve thermal conductivity (TC) and microcracking resistance. Good quality nanocomposites were fabricated and evaluated for TC and durability including radiation resistance. TC was measured in both in-plan and thru-the-thickness directions, and the effects of microcracks on TC are also being evaluated. This paper will discuss the systematic experimental approaches, various performance-durability evaluations, and current subcomponent design and fabrication/manufacturing efforts.

  11. Advances in the biomedical application of polymer-functionalized carbon nanotubes.

    PubMed

    Soleyman, Rouhollah; Hirbod, Sorina; Adeli, Mohsen

    2015-05-01

    Nowadays, carbon nanotubes (CNTs) have attracted the attention of scientists because of their unique electronic, magnetic, optical, mechanical, and chemical properties. However, their poor solubility in solvents, especially in water, limits their applications in several promising fields such as biomedicine, biomedical imaging, and cancer therapy. The attachment of hydrophilic segments to CNTs is a very efficient method for overcoming this problem. This review covers the latest advances in the synthesis of water-soluble CNTs with an emphasis on the molecular structure of various categories of hydrophilic molecules/macromolecules which have been grafted onto the surface of CNTs. Indeed, from the viewpoint of chemical synthesis, covalent bonding of several water-soluble molecules/macromolecules including small water-soluble organic molecules, linear, hyperbranched and dendritic polymers/biopolymers, glycoconjugate molecules/polymers as well as biomolecules onto the surface of CNTs has been deeply surveyed. Moreover, the most recent and interesting bio-applications of polymer-functionalized water-soluble CNTs have been properly reviewed. PMID:26222588

  12. Polymers.

    ERIC Educational Resources Information Center

    Tucker, David C.

    1986-01-01

    Presents an open-ended experiment which has students exploring polymer chemistry and reverse osmosis. This activity involves construction of a polymer membrane, use of it in a simple osmosis experiment, and application of its principles in solving a science-technology-society problem. (ML)

  13. Polymer infiltration studies

    NASA Technical Reports Server (NTRS)

    Marchello, Joseph M.

    1994-01-01

    During the past three months, significant progress has been made on the preparation of carbon fiber composites using advanced polymer resins. The results are set forth in recent reports and publications, and will be presented at forthcoming national and international meetings. Current and ongoing research activities reported herein include: textile composites from powder-coated towpreg - role of surface coating in braiding; prepregger hot sled operation in making tape from powder coated tow; ribbonizing powder-impregnated towpreg; textile composites from powder-coated towpreg - role of bulk factor in consolidation; powder curtain prepreg process improvements in doctoring of powder; and hot/cold shoe for ATP open-section part warpage control.

  14. Removal of radioactive materials and heavy metals from water using magnetic resin

    DOEpatents

    Kochen, Robert L.; Navratil, James D.

    1997-01-21

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

  15. Removal of radioactive materials and heavy metals from water using magnetic resin

    DOEpatents

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

    1997-01-21

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

  16. 21 CFR 177.1555 - Polyarylate resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

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

  17. 21 CFR 177.1555 - Polyarylate resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

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

  18. 21 CFR 177.1555 - Polyarylate resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

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

  19. 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.

  20. Structure-to-property relationships in addition cured polymers. 4: Correlations between thermo-oxidative weight losses of norbornenyl cured polyimide resins and their composites

    NASA Technical Reports Server (NTRS)

    Alston, William B.

    1992-01-01

    Relationships are identified between the thermo-oxidative stability (TOS) at 316 C of a wide variety of PMR (polymerization of monomeric reactants) addition cured polyimide resins and their corresponding graphite fiber composites. Weight loss results at 316 C confirmed the expected relationship of increasing aliphatic endcap content with decreasing TOS. Moreover, the resin TOS study also showed an unexpected linear correlation of decreasing weight loss to increasing ratio of benzylic diamine to aliphatic endcap in the range of the stoichiometries studied. Only after long term 316 C aging does the dianhydride used with the benzylic diamines become an additional factor in influencing the amount of PMR resin and composite weight losses. Also, the benzylic systems consistently showed much lower resin and composite weight losses at 316 C than the corresponding nonbenzylic norbornenyl resins and composites, except when the nonbenzylic diamine monomer does not contain a connecting group. Instead, this diamine resulted in a 316 C resin and composite weight loss that was only competitive with benzylic type diamines. Results show excellent correlation between TOS of all graphite fiber PMR composites and resins.

  1. Advanced two-photon photolithography for patterning of transparent, electrically conductive ionic liquid-polymer nanostructures

    NASA Astrophysics Data System (ADS)

    Bakhtina, Natalia A.; MacKinnon, Neil; Korvink, Jan G.

    2016-04-01

    A key challenge in micro- and nanotechnology is the direct patterning of functional structures. For example, it is highly desirable to possess the ability to create three-dimensional (3D), conductive, and optically transparent structures. Efforts in this direction have, to date, yielded less than optimal results since the polymer composites had low optical transparency over the visible range, were only slightly conductive, or incompatible with high resolution structuring. We have previously presented the novel cross-linkable, conductive, highly transparent composite material based on a photoresist (IP-L 780, OrmoComp, or SU-8) and the ionic liquid 1-butyl-3-methylimidazolium dicyanamide. Material patterning by conventional and two-photon photolithography has been demonstrated as proof-of-concept. Aiming to increase the resolution and to extend the spectrum of exciting applications we continued our research into identifying new ionic liquid - polymer composites. In this paper, we report the precise 3D single-step structuring of optically transparent and electrically conductive ionic liquid - polymer nanostructures with the highest spatial resolution (down to 150 nm) achieved to date. This was achieved via the development of novel cross-linkable composite based on the photoresist IP-G 780 and the ionic liquid 1-butyl-3-methylimidazolium dicyanamide. The successful combination of the developed material with the advanced direct laser writing technique enabled the time- and cost-saving direct manufacturing of transparent, electrically conductive components. We believe that the excellent characteristics of the structured material will open a wider range of exciting applications.

  2. Advancements in fabrication process of microelectrode array for a retinal prosthesis using Liquid Crystal Polymer (LCP).

    PubMed

    Jeong, Joonsoo; Shin, Soowon; Lee, Geun Jae; Gwon, Tae Mok; Park, Jeong Hoan; Kim, Sung June

    2013-01-01

    Liquid Crystal Polymer (LCP) has been considered as an alternative biomaterial for implantable biomedical devices primarily for its low moisture absorption rate compared with conventional polymers such as polyimide, parylene and silicone elastomers. A novel retinal prosthetic device based on monolithic encapsulation of LCP is being developed in which entire neural stimulation circuitries are integrated into a thin and eye-conformable structure. Micromachining techniques for fabrication of a LCP retinal electrode array have been previously reported. In this research, however, for being used as a part of the LCP-based retinal implant, we developed advanced fabrication process of LCP retinal electrode through new approaches such as electroplating and laser-machining in order to achieve higher mechanical robustness, long-term reliability and flexibility. Thickened metal tracks could contribute to higher mechanical strength as well as higher long-term reliability when combined with laser-ablation process by allowing high-pressure lamination. Laser-thinning technique could improve the flexibility of LCP electrode. PMID:24110931

  3. Study of mould design and forming process on advanced polymer-matrix composite complex structure

    NASA Astrophysics Data System (ADS)

    Li, S. J.; Zhan, L. H.; Bai, H. M.; Chen, X. P.; Zhou, Y. Q.

    2015-07-01

    Advanced carbon fibre-reinforced polymer-matrix composites are widely applied to aviation manufacturing field due to their outstanding performance. In this paper, the mould design and forming process of the complex composite structure were discussed in detail using the hat stiffened structure as an example. The key issues of the moulddesign were analyzed, and the corresponding solutions were also presented. The crucial control points of the forming process such as the determination of materials and stacking sequence, the temperature and pressure route of the co-curing process were introduced. In order to guarantee the forming quality of the composite hat stiffened structure, a mathematical model about the aperture of rubber mandrel was introduced. The study presented in this paper may provide some actual references for the design and manufacture of the important complex composite structures.

  4. 21 CFR 173.10 - Modified polyacrylamide resin.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

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

  5. 21 CFR 173.10 - Modified polyacrylamide resin.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

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

  6. Advanced insulations for refrigerator/freezers: The potential for new shell designs incorporating polymer barrier construction

    SciTech Connect

    Griffith, B.T.; Arasteh, D.

    1992-11-01

    The impending phase-out of chlorofluorocarbons (CFCs) used to expand foam insulation, combined with requirements for increased energy efficiency, make the use of non-CFC-based high performance insulation technologies increasingly attractive. The majority of current efforts are directed at using advanced insulations in the form of thin, flat low-conductivity gas-filled or evacuated orthogonal panels, which we refer to as Advanced Insulation Panels (AIPs). AIPs can be used in composite with blown polymer foams to improve insulation performance in refrigerator/freezers (R/Fs) of conventional design and manufacture. This AIP/foam composite approach is appealing because it appears to be a feasible, near-term method for incorporating advanced insulations into R/Fs without substantial redesign or retooling. However, the requirements for adequate flow of foam during the foam-in-place operation impose limitations on the allowable thickness and coverage area of AIPs. This report examines design alternatives which may offer a greater increase in overall thermal resistance than is possible with the use of AIP/foam composites in current R/F design. These design alternatives generally involve a basic redesign of the R/F taking into account the unique requirements of advanced insulations and the importance of minimizing thermal bridging with high thermal resistance insulations. The focus here is on R/F doors because they are relatively simple and independent R/F components and are therefore good candidates for development of alterative designs. R/F doors have significant thermal bridging problems due to the steel outer shell construction. A three dimensional finite difference computer modeling exercise of a R/F door geometry was used to compare the overall levels of thermal resistance (R-value) for various design configurations.

  7. Final Technical Report - Advanced Optical Sensors to Minimize Energy Consumption in Polymer Extrusion Processes

    SciTech Connect

    Susan J. Foulk

    2012-07-24

    Project Objective: The objectives of this study are to develop an accurate and stable on-line sensor system to monitor color and composition on-line in polymer melts, to develop a scheme for using the output to control extruders to eliminate the energy, material and operational costs of off-specification product, and to combine or eliminate some extrusion processes. Background: Polymer extrusion processes are difficult to control because the quality achieved in the final product is complexly affected by the properties of the extruder screw, speed of extrusion, temperature, polymer composition, strength and dispersion properties of additives, and feeder system properties. Extruder systems are engineered to be highly reproducible so that when the correct settings to produce a particular product are found, that product can be reliably produced time after time. However market conditions often require changes in the final product, different products or grades may be processed in the same equipment, and feed materials vary from lot to lot. All of these changes require empirical adjustment of extruder settings to produce a product meeting specifications. Optical sensor systems that can continuously monitor the composition and color of the extruded polymer could detect process upsets, drift, blending oscillations, and changes in dispersion of additives. Development of an effective control algorithm using the output of the monitor would enable rapid corrections for changes in materials and operating conditions, thereby eliminating most of the scrap and recycle of current processing. This information could be used to identify extruder systems issues, diagnose problem sources, and suggest corrective actions in real-time to help keep extruder system settings within the optimum control region. Using these advanced optical sensor systems would give extruder operators real-time feedback from their process. They could reduce the amount of off-spec product produced and

  8. Advanced polymer PV system: PVMaT 4A1 annual report, September 1995--September 1996

    SciTech Connect

    Hanoka, J; Chleboski, R; Farber, M; Fava, J; Kane, P; Martz, J

    1997-06-01

    Purpose of this subcontract was to produce lower module and systems costs through the innovative use of polymeric materials. The Innovative Mounting System (IMS) was developed and testing begun during the first year of this contract. IMS reduces the cost of installed PV systems by reducing labor and materials costs both in the factory and in field installation. It incorporates several advances in polymers, processing methods and product design. An advanced backskin material permits elimination of the conventional Al perimeter frame by protecting and sealing the edge and by direct bonding of multifunctional mounting bars. Electrical interconnection is easier and more reliable with a new junction box. Feasibility of a non-vacuum, high-throughput lamination method was also demonstrated, involving a novel transparent encapsulant with UV stabilization package that can be laminated in air and which should lead to longer field life than conventional designs. The first-year program culminated in the fielding of prototype products with the new encapsulant, backskin, junction box, frameless edge seal, and IMS. Feedback and marketing information from potential customers were solicited. Result promises a $0.50/watt manufacturing and system cost reductions as well as increased system lifetime. The second year will complete refinement and test of the encapsulant and backskin, complete the new lamination method, and refine product designs.

  9. Advanced Polymer Technology for Containing and Immobilizing Strontium-90 in the Subsurface - 8361

    SciTech Connect

    K. Baker; G. Heath; C. Scott; A. Schafer; S. Bryant; M. Sharma; C. Huh; S. K. Choi

    2008-02-01

    Many Department of Energy (DOE) sites, including Idaho and Hanford, have heavy metals and/or radionuclides (e.g. strontium-90) present that are strongly adsorbed in the vadose zone, but which nevertheless are propagating toward the water table. A key challenge for immobilization of these contaminants is bringing the chosen amendment or remediation technology into contact with the contaminated porous medium, while ensuring that contaminated water and colloids do not escape. This is particularly challenging when the subsurface geology is complex and highly heterogeneous, as is the case at many DOE sites. The Idaho National Laboratory (INL) in collaboration with the University of Texas at Austin (UT) has conducted research sponsored through the DOE Office of Environmental Management (EM) Advanced Remediation Technologies Phase I program that successfully demonstrated application of a novel, pH-triggered advanced polymer for creating a physical barrier that prevents heavy metals and radionuclides in vadose zone soil and soil-pore water from migrating to the groundwater. The focus of this paper is on the column and sandbox experiments conducted by researchers at the Idaho National Laboratory in support of the Phase I program objectives. Proof of these concepts provides a technology basis for confining or isolating a volume of contaminated groundwater, to be implemented in future investigations at the Vadose Zone Research Park (VZRP) at INL.

  10. 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.

  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. 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.

  13. Maleimide Functionalized Siloxane Resins

    SciTech Connect

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

    1999-04-01

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

  14. Smart Materials for Advanced Applications: Self-Decontaminating Polymers, Photofunctional Composites, and Electroconductive Fibers

    NASA Astrophysics Data System (ADS)

    Little, Brian Kevin

    2011-12-01

    Materials capable of providing multifunctional properties controllable by some external stimulus (pH, light, temperature, etc) are highly desirable and obtainable given recent advancements in material science. Development of these so called "Smart" materials spanned across many disciplines of science with applications in industrial areas such as medical, military, security, and environmental. Furthermore, next-generation materials require the ability to not only sense/respond to changes in their external/internal environment, but process information in regards to these changes and adapt accordingly in a dynamic fashion, autonomously, so called "Intelligent" materials. Findings reported in this manuscript detail the synthesis, characterization, and application of smart materials in the following three areas: (1) self-cleaning polymers (2) photoresponsive composites and (3) electroconductive fibers. Self-Cleaning Polymers: Self-decontaminating polymers are unique materials capable of degrading toxic organic chemicals (TOCs). Barriers composed of or coated with our photochemical reactive polymer matrix could be applied to multiple surfaces for defense against TOCs; for example, military garments for protection against chemical warfare agents. This study investigates conditions necessary for formation of peroxides via O2 reduction induced by long-lived, strongly reducing benzophenyl ketyl (BPK) polymer radicals. Photolysis of aqueous solutions composed of sulphonated poly(ether etherketone), SPEEK, and poly(vinyl alcohol), PVA lead to the formation of the BPK radicals. Experiments investigate the formation and decomposition of peroxides in aqueous solutions of SPEEK/PVA under photolysis. Photofunctional Composites: Photoresponsive nanoporous (PN) films and powders were studied and evaluated as possible additives to sensitize the initiation of CH3NO2 via a mechanism involving coalescence of reaction sites. Such materials consist of a 3-D mesoporous silica framework

  15. INDUSTRIAL PROCESS PROFILES FOR ENVIRONMENTAL USE. CHAPTER 10A. THE PLASTICS AND RESINS PROCESSING INDUSTRY

    EPA Science Inventory

    The report contains a detailed analysis of the plastics and resins processing industry, which includes operations that convert polymers and resins into consumer products. Analytical elements include industry definition, raw materials, products, manufacturers, environmental impact...

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

    PubMed

    Ohe, Y; Kadoma, Y; Imai, Y

    1989-07-01

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

  17. Advances in solid polymer electrolyte fuel cell technology with low-platinum-loading electrodes

    NASA Technical Reports Server (NTRS)

    Srinivasan, Supramaniam; Ticianelli, E. A.; Derouin, C. R.; Redondo, A.

    1987-01-01

    The Gemini Space program demonstrated the first major application of fuel cell systems. Solid polymer electrolyte fuel cells were used as auxiliary power sources in the spacecraft. There has been considerable progress in this technology since then, particularly with the substitution of Nafion for the polystyrene sulfonate membrane as the electrolyte. Until recently the performance was good only with high platinum loading (4 mg/sq cm) electrodes. Methods are presented to advance the technology by (1) use of low platinum loading (0.35 mg/sq cm) electrodes; (2) optimization of anode/membrane/cathode interfaces by hot pressing; (3) pressurization of reactant gases, which is most important when air is used as cathodic reactant; and (4) adequate humidification of reactant gases to overcome the water management problem. The high performance of the fuel cell with the low loading of platinum appears to be due to the extension of the three dimensional reaction zone by introduction of a proton conductor, Nafion. This was confirmed by cyclic voltammetry.

  18. Conducting polymer blends: Polypyrrole and polythiophene blends with polystyrene, polycarbonate resin, poly(vinyl alcohol) and poly(vinyl methyl ketone)

    SciTech Connect

    Wang, H.L.

    1992-01-01

    Various aromatic compounds can be polymerized by electrochemical oxidation in solution containing a supporting electrolyte. Most studies have been devoted to polypyrrole and polythiophene. In situ doping during electrochemical polymerization yields free standing conductive polymer film. One major approach to making conducting polymer blends is electrochemical synthesis after coating the host polymer on a platinum electrode. In the electrolysis of pyrrole or thiophene monomer, using (t-Bu[sub 4]N)BF[sub 4] as supporting electrolyte, and acetonitrile as solvent, monomer can diffuse through the polymer film, to produce a polypyrrole or polythiophene blend in the film. Doping occurs along with polymerization to form a conducting polymer alloy. The strongest molecular interaction in polymers, and one that is central to phase behavior, is hydrogen bonding. This mixing at the molecular level enhances the degree of miscibility between two polymers and results in macroscopic properties indicative of single phase behavior. In this dissertation, the authors describes the syntheses of conducting polymer blends: polypyrrole and polythiophene blends with polystyrene, poly(bisphenol-A-carbonate), polyvinyl alcohol and poly(vinyl methyl ketone). The syntheses are performed both electrochemically and chemically. Characterization of these blends was carried out by Fourier Transform Infrared spectroscopy, Differential Scanning Calorimetry, Thermogravimetric Analysis, Scanning Electron Microscopy, and X-ray diffraction. Percolating threshold conductivities occur from 7% to 20% for different polymer blends. The low threshold conductivity is attributed to blend homogeneity enhanced by hydrogen bonding between the carbonyl group in the insulating polymer and the N-H group in polypyrrole. Thermal stability, environmental stability, mechanical properties, crystallinity and morphological structure are also discussed. The authors have also engaged in the polymerization of imidazoles.

  19. Recent advances in solid polymer electrolyte fuel cell technology with low platinum loading electrodes

    NASA Technical Reports Server (NTRS)

    Srinivasan, Supramaniam; Manko, David J.; Enayatullah, Mohammad; Appleby, A. John

    1989-01-01

    High power density fuel cell systems for defense and civilian applications are being developed. Taking into consideration the main causes for efficiency losses (activation, mass transport and ohmic overpotentials) the only fuel cell systems capable of achieving high power densities are the ones with alkaline and solid polymer electrolyte. High power densities (0.8 W/sq cm at 0.8 V and 1 A/sq cm with H2 and O2 as reactants), were already used in NASA's Apollo and Space Shuttle flights as auxiliary power sources. Even higher power densities (4 W/sq cm - i.e., 8 A sq cm at 0.5 V) were reported by the USAF/International Fuel Cells in advanced versions of the alkaline system. High power densities (approximately 1 watt/sq cm) in solid polymer electrolyte fuel cells with ten times lower platinum loading in the electrodes (i.e., 0.4 mg/sq cm) were attained. It is now possible to reach a cell potential of 0.620 V at a current density of 2 A/sq cm and at a temperature of 95 C and pressure of 4/5 atm with H2/O2 as reactants. The slope of the linear region of the potential-current density plot for this case is 0.15 ohm-sq cm. With H2/air as reactants and under the same operating conditions, mass transport limitations are encountered at current densities above 1.4 A/sq cm. Thus, the cell potential at 1 A/sq cm with H2/air as reactants is less than that with H2/O2 as reactants by 40 mV, which is the expected value based on electrode kinetics of the oxygen reduction reaction, and at 2 A/sq cm with H2/air as reactant is less than the corresponding value with H2/O2 as reactants by 250 mV, which is due to the considerably greater mass transport limitations in the former case.

  20. Development and testing of new biologically-based polymers as advanced biocompatible contact lenses

    SciTech Connect

    Bertozzi, Carolyn R.

    2000-06-01

    Nature has evolved complex and elegant materials well suited to fulfill a myriad of functions. Lubricants, structural scaffolds and protective sheaths can all be found in nature, and these provide a rich source of inspiration for the rational design of materials for biomedical applications. Many biological materials are based in some fashion on hydrogels, the crosslinked polymers that absorb and hold water. Biological hydrogels contribute to processes as diverse as mineral nucleation during bone growth and protection and hydration of the cell surface. The carbohydrate layer that coats all living cells, often referred to as the glycocalyx, has hydrogel-like properties that keep cell surfaces well hydrated, segregated from neighboring cells, and resistant to non-specific protein deposition. With the molecular details of cell surface carbohydrates now in hand, adaptation of these structural motifs to synthetic materials is an appealing strategy for improving biocompatibility. The goal of this collaborative project between Prof. Bertozzi's research group, the Center for Advanced Materials at Lawrence Berkeley National Laboratory and Sunsoft Corporation was the design, synthesis and characterization of novel hydrogel polymers for improved soft contact lens materials. Our efforts were motivated by the urgent need for improved materials that allow extended wear, and essential feature for those whose occupation requires the use of contact lenses rather than traditional spectacles. Our strategy was to transplant the chemical features of cell surface molecules into contact lens materials so that they more closely resemble the tissue in which they reside. Specifically, we integrated carbohydrate molecules similar to those found on cell surfaces, and sulfoxide materials inspired by the properties of the carbohydrates, into hydrogels composed of biocompatible and manufacturable substrates. The new materials were characterized with respect to surface and bulk hydrophilicity, and

  1. High-temperature resins

    NASA Technical Reports Server (NTRS)

    Serafini, T. T.

    1982-01-01

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

  2. 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.

  3. Cesium-specific phenolic ion exchange resin

    DOEpatents

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

    1995-08-15

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

  4. Advanced Process Model for Polymer Pyrolysis and Uranium Ceramic Material Processing

    SciTech Connect

    Wang, Xiaolin; Zunjarrao, Suraj C.; Zhang, Hui; Singh, Raman P.

    2006-07-01

    Silicon carbide (SiC) based uranium ceramic material can be fabricated as hosts for ultra high temperature applications, such as gas-cooled fast reactor fuels and in-core materials. A pyrolysis-based material processing technique allows for the fabrication of SiC based uranium ceramic materials at a lower temperature compared to sintering route. Modeling of the process is considered important for optimizing the fabrication and producing material with high uniformity. This study presents a process model describing polymer pyrolysis and uranium ceramic material processing, including heat transfer, polymer pyrolysis, SiC crystallization, chemical reactions, and species transport of a porous uranium oxide mixed polymer. Three key reactions for polymer pyrolysis and one key reaction for uranium oxide polymer interaction are established for the processing. Included in the model formulation are the effects of transport processes such as heat-up, polymer decomposition, and volatiles escape. The model is capable of accurately predicting the polymer pyrolysis and chemical reactions of the source material. Processing of a sample with certain geometry is simulated. The effects of heating rate, particle size and volume ratio of uranium oxide and polymer on porosity evolution, species uniformity, reaction rate are investigated. (authors)

  5. 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.

  6. 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.

  7. 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.

  8. 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.

  9. Phase I study of capecitabine combined with radioembolization using yttrium-90 resin microspheres (SIR-Spheres) in patients with advanced cancer

    PubMed Central

    Cohen, S J; Konski, A A; Putnam, S; Ball, D S; Meyer, J E; Yu, J Q; Astsaturov, I; Marlow, C; Dickens, A; Cade, D N; Meropol, N J

    2014-01-01

    Background: This was a prospective single-centre, phase I study to document the maximum tolerated dose (MTD), dose-limiting toxicity (DLT), and the recommended phase II dose for future study of capecitabine in combination with radioembolization. Methods: Patients with advanced unresectable liver-dominant cancer were enrolled in a 3+3 design with escalating doses of capecitabine (375–1000 mg/m2 b.i.d.) for 14 days every 21 days. Radioembolization with 90Y-resin microspheres was administered using a sequential lobar approach with two cycles of capecitabine. Results: Twenty-four patients (17 colorectal) were enrolled. The MTD was not reached. Haematologic events were generally mild. Common grade 1/2 non-haematologic toxicities included transient transaminitis/alkaline phosphatase elevation (9 (37.5%) patients), nausea (9 (37.5%)), abdominal pain (7 (29.0%)), fatigue (7 (29.0%)), and hand-foot syndrome or rash/desquamation (7 (29.0%)). One patient experienced a partial gastric antral perforation with a capecitabine dose of 750 mg/m2. The best response was partial response in four (16.7%) patients, stable disease in 17 (70.8%) and progression in three (12.5%). Median time to progression and overall survival of the metastatic colorectal cancer cohort was 6.4 and 8.1 months, respectively. Conclusions: This combined modality treatment was generally well tolerated with encouraging clinical activity. Capecitabine 1000 mg/m2 b.i.d. is recommended for phase II study with sequential lobar radioembolization. PMID:24983373

  10. Synthesis, characterization and anti-microbial activity of phenylurea-formaldehyde resin (PUF) and its polymer metal complexes (PUF-Mn(II)

    NASA Astrophysics Data System (ADS)

    Ahamad, Tansir; Alshehri, Saad M.

    2012-10-01

    Phenylurea-formaldehyde polymer (PUF) was synthesized via polycondensation of phenylurea and formaldehyde in basic medium, its polymer-metal complexes [PUF-M(II)] were prepared with Mn(II), Co(II), Ni(II), Cu(II), and Zn(II) ions. PUF and PUF-M(II) were characterized with magnetic moment measurements, elemental and spectral (UV-visible, FTIR, 1H-NMR, 13C-NMR and ESR) analysis. The thermal behaviors of all the synthesized polymers were carried out using thermogravimetric analysis (TGA) and differential thermal analysis (DTA). The thermal data revealed that all of the PUF-M(II) showed higher thermal stabilities than the PUF and also ascribed that the PUF-Cu(II) showed better thermal stability than the other PUF-M(II). The kinetic parameters such as activation energy, pre-exponential factor etc., were evaluated for these polymer metal complexes using Coats-Redfern equation. In addition, the antimicrobial activity of the synthesized polymers was tested against several microorganisms using agar well diffusion methods. Among all of the PUF-M(II), the antimicrobial activity of the PUF-Cu(II) showed the highest zone of inhibition because of its higher stability constant and may be used in biomedical applications.

  11. Electrophysical behavior of ion-conductive organic-inorganic polymer system based on aliphatic epoxy resin and salt of lithium perchlorate

    NASA Astrophysics Data System (ADS)

    Matkovska, Liubov; Iurzhenko, Maksym; Mamunya, Yevgen; Matkovska, Olga; Demchenko, Valeriy; Lebedev, Eugene; Boiteux, Gisele; Serghei, Anatoli

    2014-12-01

    In the present work, ion-conductive hybrid organic-inorganic polymers based on epoxy oligomer of diglycide aliphatic ester of polyethylene glycol (DEG) and lithium perchlorate (LiClO4) were synthesized. The effect of LiClO4 content on the electrophysical properties of epoxy polymers has been studied by differential scanning calorimetry (DSC) and broadband dielectric spectroscopy (BDS). The effect of LiClO4 content on the structure has been studied by wide-angle X-ray scattering (WAXS). It was found that LiClO4 impacts on the structure of the synthesized hybrid epoxy polymers, probably, by formation of coordinative complexes {ether oxygen-lithium cations-ether oxygen} as evidenced from a significant increase in their glass transition temperatures with increasing LiClO4 concentration and WAXS studies. The presence of ether oxygen in DEG macromolecules provides a transfer mechanism of the lithium cations with the ether oxygen similar to polyethylene oxide (PEO). Thus, the obtained hybrid polymers have high values of ionic conductivity σ' (approximately 10-3 S/cm) and permittivity ɛ' (6 × 105) at elevated temperatures (200°C). On the other hand, DEG has higher heat resistance compared to PEO that makes these systems perspective as solid polymer electrolytes able to operate at high temperature.

  12. Resinous binders for coal and chars

    SciTech Connect

    Olson, E.S.; Sharma, R.K.; Young, B.C.

    1995-12-31

    Binder development and application to the briquetting or pelleting of coal fines has been extensive. The search for low-cost, effective binders for making strong and durable briquettes or pellets continues unabated. Strong, durable compacts are required, not only for handling, transport, and storage of the product but also to withstand the rigors of application such as flue gas treatment sorbents and catalytic supports. Many kinds of binders, organic and inorganic, have been used to gain the desired strength. Synthetic polymers have been investigated because they promote good strength and water insolubility, but these features are generally outweighed by the polymer cost. Promising earlier developments of biomass-derived binders have received slow market acceptance, mainly because of the cost resulting from the high concentrations required. However, recent advances in processing lignocellulosic materials have generated potentially low-cost polymeric binding agents for making coal briquettes. Phenol novolaks were previously used with lignites to make activated carbons. Recently, binders were prepared from mixtures of phenol, lignin, and formaldehyde and used for wood flour molding and friction materials. The goal of our work was to investigate the characteristics of resinous binders from lignocellulosic as well as coal-derived materials when used with dried or beneficiated coals and chars.

  13. Electron Beam Cured Epoxy Resin Composites for High Temperature Applications

    NASA Technical Reports Server (NTRS)

    Janke, Christopher J.; Dorsey, George F.; Havens, Stephen J.; Lopata, Vincent J.; Meador, Michael A.

    1997-01-01

    Electron beam curing of Polymer Matrix Composites (PMC's) is a nonthermal, nonautoclave curing process that has been demonstrated to be a cost effective and advantageous alternative to conventional thermal curing. Advantages of electron beam curing include: reduced manufacturing costs; significantly reduced curing times; improvements in part quality and performance; reduced environmental and health concerns; and improvement in material handling. In 1994 a Cooperative Research and Development Agreement (CRADA), sponsored by the Department of Energy Defense Programs and 10 industrial partners, was established to advance the electron beam curing of PMC technology. Over the last several years a significant amount of effort within the CRADA has been devoted to the development and optimization of resin systems and PMCs that match the performance of thermal cured composites. This highly successful materials development effort has resulted in a board family of high performance, electron beam curable cationic epoxy resin systems possessing a wide range of excellent processing and property profiles. Hundreds of resin systems, both toughened and untoughened, offering unlimited formulation and processing flexibility have been developed and evaluated in the CRADA program.

  14. Advances in engineering plastics

    SciTech Connect

    Leonard, L.

    1997-12-01

    New polymers are being commercialized in record numbers, offering the product designer a new realm of possibilities, and promising tough competition to the traditional engineering resins. Most of the growth is in single-site catalyzed resins. Metallocene (and non-metallocene) single-site catalysts enhance polymer architecture to generate highly uniform molecules, and even permit tailoring new categories of polymers. These new materials include the truly unique aliphatic polyketone, syndiotactic polystyrene (SPS); polyethylene naphthalate (PEN) resins; and novel variations of established polymers. This article provides a closer look at these newcomers to the plastics marketplace, with an emphasis on their properties and potential applications.

  15. Polyimide resins

    DOEpatents

    Tesoro, Giuliana C.; Sastri, Vinod R.

    1993-01-01

    A method for the preparation of a polyimide containing reversible crosslinks comprising the step of curing a monomer having the formula ##STR1## wherein R and R' may be the same or different and each is H or lower alkyl having 1-5 carbon atoms under conditions conducive to the formation of a polyimide and thereby forming a polyimide having the formula ##STR2## R and R' are as defined above and n is an integer from 10 to 100. The polyimide may be converted to a soluble polymer by cleaving the disulfide bond in the presence of a solvent and a reducing agent. The reduced polymer may be reformed into the polymer in an oxidation step or into a modified polyimide in other reaction steps. Copolymerization processes are also disclosed.

  16. Electrically conductive polymer concrete overlays

    NASA Astrophysics Data System (ADS)

    Fontana, J. J.; Webster, R. P.

    1984-08-01

    The use of cathodic protection to prevent the corrosion of reinforcing steel in concrete structures has been well established. Application of a durable, skid-resistant electrically conductive polymer concrete overlay would advance the use of cathodic protection for the highway industry. Laboratory studies indicate that electrically conductive polymer concrete overlays using conductive fillers, such as calcined coke breeze, in conjunction with polyester or vinyl ester resins have resistivities of 1 to 10 ohm-cm. Both multiple-layer and premixed mortar-type overlays were made. Shear bond strengths of the conductive overlays to concrete substrates vary from 600 to 1300 psi, with the premixed overlays having bond strengths 50 to 100% higher than the multiple-layer overlays.

  17. 21 CFR 173.25 - Ion-exchange resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

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

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

    NASA Technical Reports Server (NTRS)

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

    1988-01-01

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

  19. Atomic step-and-terrace surface of polyimide sheet for advanced polymer substrate engineering.

    PubMed

    Tan, G; Shimada, K; Nozawa, Y; Kaneko, S; Urakami, T; Koyama, K; Komura, M; Matsuda, A; Yoshimoto, M

    2016-07-22

    Typical thermostable and flexible polyimide polymers exhibit many excellent properties such as strong mechanical and chemical resistance. However, in contrast to single-crystal substrates like silicon or sapphire, polymers mostly display disordered and rough surfaces, which may result in instability and degradation of the interfaces between thin films and polymer substrates. As a step toward the development of next-generation polymer substrates, we here report single-atom-layer imprinting onto the polyimide sheets, resulting in an ultrasmooth 0.3 nm high atomic step-and-terrace surface on the polyimides. The ultrasmooth polymer substrates are expected to be applied to the fabrication of nanostructures such as superlattices, nanowires, or quantum dots in nanoscale-controlled electronic devices. We fabricate smooth and atomically stepped indium tin oxide transparent conducting oxide thin films on the imprinted polyimide sheets for future use in organic-based optoelectronic devices processed with nanoscale precision. Furthermore, toward 2D polymer substrate nanoengineering, we demonstrate nanoscale letter writing on the atomic step-and-terrace polyimide surface via atomic force microscopy probe scratching. PMID:27284690

  20. Atomic step-and-terrace surface of polyimide sheet for advanced polymer substrate engineering

    NASA Astrophysics Data System (ADS)

    Tan, G.; Shimada, K.; Nozawa, Y.; Kaneko, S.; Urakami, T.; Koyama, K.; Komura, M.; Matsuda, A.; Yoshimoto, M.

    2016-07-01

    Typical thermostable and flexible polyimide polymers exhibit many excellent properties such as strong mechanical and chemical resistance. However, in contrast to single-crystal substrates like silicon or sapphire, polymers mostly display disordered and rough surfaces, which may result in instability and degradation of the interfaces between thin films and polymer substrates. As a step toward the development of next-generation polymer substrates, we here report single-atom-layer imprinting onto the polyimide sheets, resulting in an ultrasmooth 0.3 nm high atomic step-and-terrace surface on the polyimides. The ultrasmooth polymer substrates are expected to be applied to the fabrication of nanostructures such as superlattices, nanowires, or quantum dots in nanoscale-controlled electronic devices. We fabricate smooth and atomically stepped indium tin oxide transparent conducting oxide thin films on the imprinted polyimide sheets for future use in organic-based optoelectronic devices processed with nanoscale precision. Furthermore, toward 2D polymer substrate nanoengineering, we demonstrate nanoscale letter writing on the atomic step-and-terrace polyimide surface via atomic force microscopy probe scratching.

  1. Polymer infiltration studies

    NASA Technical Reports Server (NTRS)

    Marchello, Joseph M.

    1992-01-01

    Significant progress has been made during the past three months on the preparation of carbon fiber composites using advanced polymer resins. The results are set forth in recent reports and publications, and will be presented at forthcoming national and international meetings. Current and ongoing research activities reported herein include: powdered tow ribbonizing; unitape from powdered tow; customized towpreg for textiles and ATP; and textile composite research. During the period ahead research will be directed toward further development of the new powder curtain prepregging method and on ways to customize dry powder towpreg for textile and robotic applications in aircraft part fabrication. Studies of multi-tow powder prepregging and ribbon preparation will be initiated in conjunction with continued development of prepregging technology and the various aspects of composite part fabrication using customized towpreg. Also, a major effort during the coming months will be participating in the analysis of the performance of the new solution prepregger.

  2. Polymer Infiltration Studies

    NASA Technical Reports Server (NTRS)

    Marchello, Joseph M.

    1993-01-01

    Significant progress has been made on the preparation of carbon fiber composites using advanced polymer resins during the past three months. Current and ongoing research activities reported herein include: (1) Prepregger Hot Sled Operation; (2) Ribbonizing Powder-Impregnated Towpreg; (3) Textile Composites from Powder-Coated Towpreg: Role of Bulk Factor; and (4) Powder Curtain Prepreg Process. During the coming months research will be directed toward further development of the new powder curtain prepregging method and on ways to customize dry powder towpreg for textile and robotic applications in aircraft part fabrication. Studies of multi-tow powder prepregging and ribbon preparation will be conducted in conjunction with continued development of prepegging technology and the various aspects of composite part fabrication using customized towpreg. Also, work will continue on the analysis of the new solution prepegger.

  3. 21 CFR 173.25 - Ion-exchange resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ...,” February 4, 1998, which is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ion-exchange resins. 173.25 Section 173.25 Food... Polymer Substances and Polymer Adjuvants for Food Treatment § 173.25 Ion-exchange resins....

  4. 21 CFR 173.25 - Ion-exchange resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ...,” February 4, 1998, which is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ion-exchange resins. 173.25 Section 173.25 Food... Polymer Substances and Polymer Adjuvants for Food Treatment § 173.25 Ion-exchange resins....

  5. 21 CFR 173.25 - Ion-exchange resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ...,” February 4, 1998, which is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ion-exchange resins. 173.25 Section 173.25 Food... Polymer Substances and Polymer Adjuvants for Food Treatment § 173.25 Ion-exchange resins....

  6. Aqueous vinylidene fluoride polymer coating composition

    NASA Technical Reports Server (NTRS)

    Bartoszek, Edward J. (Inventor); Christofas, Alkis (Inventor)

    1978-01-01

    A water-based coating composition which may be air dried to form durable, fire resistant coatings includes dispersed vinylidene fluoride polymer particles, emulsified liquid epoxy resin and a dissolved emulsifying agent for said epoxy resin which agent is also capable of rapidly curing the epoxy resin upon removal of the water from the composition.

  7. Recent advances in solid polymer electrolyte fuel cell technology with low platinum loading electrodes

    NASA Technical Reports Server (NTRS)

    Srinivasan, Supramaniam; Manko, David J.; Koch, Hermann; Enayetullah, Mohammad A.; Appleby, A. John

    1989-01-01

    Of all the fuel cell systems only alkaline and solid polymer electrolyte fuel cells are capable of achieving high power densities (greater than 1 W/sq cm) required for terrestrial and extraterrestrial applications. Electrode kinetic criteria for attaining such high power densities are discussed. Attainment of high power densities in solid polymer electrolyte fuel cells has been demonstrated earlier by different groups using high platinum loading electrodes (4 mg/sq cm). Recent works at Los Alamos National Laboratory and at Texas A and M University (TAMU) demonstrated similar performance for solid polymer electrolyte fuel cells with ten times lower platinum loading (0.45 mg/sq cm) in the electrodes. Some of the results obtained are discussed in terms of the effects of type and thickness of membrane and of the methods platinum localization in the electrodes on the performance of a single cell.

  8. The nature and fate of natural resins in the geosphere. XI.{sup +} ruthenium tetroxide oxidation in a mature class Ib amber polymer.

    SciTech Connect

    Anderson, K. B.; Chemistry

    2001-01-01

    The results of ruthenium tetroxide (RuO{sub 4}) oxidation of a mature Class Ib amber polymer are reported and discussed. These data indicate that the residual double bond present in mature Class I ambers is not located in the A/B ring structure of these materials and that C17 of the original labdanoid precursors is retained in mature Class I ambers as a methyl group. These data also suggest that the reaction which results in formation of the residual unsaturated structure in mature ambers also results in a second covalent connection between the A/B ring system and the polymer backbone, probably through C8 of the original labdanoid structure.

  9. 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

  10. Threaded molecular wires as building blocks for advanced polymer blends: WPLEDs, ultra-broadband optical amplifiers, multi color lasers

    NASA Astrophysics Data System (ADS)

    Brovelli, Sergio; Mroz, Marta; Sforazzini, Giuseppe; Virgili, Tersilla; Meinardi, Franco; Paleari, Alberto; Anderson, Harry L.; Lanzani, Guglielmo; Cacialli, Franco

    2011-03-01

    The ability to produce semiconducting polymer blends with white emission spectra, large emission cross sections and broad optical gain is critical to their application in white PLEDs, lasers and broadband amplifiers. Cyclodextrin-encapsulation is an effective means of suppressing detrimental intermolecular interactions, and energy transfer (ET) channels in polymer blends, thus enabling fabrication of white-PLEDs. We show that all such properties combine into a high impact photonic application: ultra-broad optical gain and two-color lasing in a binary polyrotaxane blend. We study the ultrafast photophysics of a blend of a conventional and an encapsulated polyfluorene. The morphology is investigated by microRaman imaging, AFM, and fluorescence lifetime microscopy. We ascribe the ultra-broad optical gain (>850 meV), and the simultaneous ASE for both constituents, to the dual effect of reduced polaron formation and suppressed ET. Our results demonstrate that polyrotaxanes could realistically represent the building blocks for advanced polymer blends with highly controlled optical properties, for applications in solid state lightning, lasers and photovoltaic technologies.

  11. Review on recent and advanced applications of monoliths and related porous polymer gels in micro-fluidic devices.

    PubMed

    Vázquez, Mercedes; Paull, Brett

    2010-06-01

    This review critically summarises recent novel and advanced achievements in the application of monolithic materials and related porous polymer gels in micro-fluidic devices appearing within the literature over the period of the last 5 years (2005-2010). The range of monolithic materials has developed rapidly over the past decade, with a diverse and highly versatile class of materials now available, with each exhibiting distinct porosities, pore sizes, and a wide variety of surface functionalities. A major advantage of these materials is their ease of preparation in micro-fluidic channels by in situ polymerisation, leading to monolithic materials being increasingly utilised for a larger variety of purposes in micro-fluidic platforms. Applications of porous polymer monoliths, silica-based monoliths and related homogeneous porous polymer gels in the preparation of separation columns, ion-permeable membranes, preconcentrators, extractors, electrospray emitters, micro-valves, electrokinetic pumps, micro-reactors and micro-mixers in micro-fluidic devices are discussed herein. Procedures used in the preparation of monolithic materials in micro-channels, as well as some practical aspects of the micro-fluidic chip fabrication are addressed. Recent analytical/bioanalytical and catalytic applications of the final micro-fluidic devices incorporating monolithic materials are also reviewed. PMID:20493286

  12. 21 CFR 189.300 - Hydrogenated 4,4′-isopropyl-idene-diphenol-phosphite ester resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... weight in the range of 2,400 to 3,000. They are synthetic chemicals not found in natural products and have been used as antioxidants and as stabilizers in vinyl chloride polymer resins when such polymer resins are used in the manufacture of rigid vinyl chloride polymer bottles. (b) Food containing any...

  13. 21 CFR 189.300 - Hydrogenated 4,4′-isopropyl-idene-diphenol-phosphite ester resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...,400 to 3,000. They are synthetic chemicals not found in natural products and have been used as antioxidants and as stabilizers in vinyl chloride polymer resins when such polymer resins are used in the manufacture of rigid vinyl chloride polymer bottles. (b) Food containing any added or detectable levels...

  14. Study on dehydrochlorination of waste poly (vinyl chloride) resins by microwave irradiation

    NASA Astrophysics Data System (ADS)

    Moriwaki, Saburo; Qian, Qingrong; Sunohara, Satoshi; Machida, Motoi; Tatsumoto, Hideki

    Waste poly (vinyl chloride: PVC) resins are experimentally dehydrochlorinated by microwave irradiation. The following unique results are obtained: (1) plasticizer in PVC resin absorbs microwave power more effectively than PVC polymer. The higher the plasticizer content in PVC resin, the higher is the dehydrochlorination reaction (2) low PVC polymer content materials such as cushion floor require high microwave irradiation power to secure a high dehydrochlorination yield, (3) calcium carbonate in PVC resin reacts with released hydrochloric acid gas and results calcium chloride during microwave irradiation, (4) additives in PVC resin strongly influence dehydrochlorination yield, (5) it is evidenced that the PVC copolymer is also dehydrochlorinated by microwave irradiation.

  15. Erosion Coatings for High-Temperature Polymer Composites: A Collaborative Project With Allison Advanced Development Company

    NASA Technical Reports Server (NTRS)

    Sutter, James K.

    2000-01-01

    The advantages of replacing metals in aircraft turbine engines with high-temperature polymer matrix composites (PMC's) include weight savings accompanied by strength improvements, reduced part count, and lower manufacturing costs. Successfully integrating high-temperature PMC's into turbine engines requires several long-term characteristics. Resistance to surface erosion is one rarely reported property of PMC's in engine applications because PMC's are generally softer than metals and their erosion resistance suffers. Airflow rates in stationary turbine engine components typically exceed 2.3 kg/sec at elevated temperatures and pressures. In engine applications, as shown in the following photos, the survivability of PMC components is clearly a concern, especially when engine and component life-cycle requirements become longer. Although very few publications regarding the performance of erosion coatings on PMC's are available particularly in high-temperature applications the use of erosion-resistant coatings to significantly reduce wear on metallic substrates is well documented. In this study initiated by the NASA Glenn Research Center at Lewis Field, a low-cost (less than $140/kg) graphite-fiber-reinforced T650 35/PMR 15 sheet-molding compound was investigated with various coatings. This sheet-molding compound has been compression molded into many structurally complicated components, such as shrouds for gas turbine inlet housings and gearboxes. Erosion coatings developed for PMC s in this study consisted of a two-layered system: a bondcoat sprayed onto a cleaned PMC surface, followed by an erosion-resistant, hard topcoat sprayed onto the bondcoat as shown in following photomicrograph. Six erosion coating systems were evaluated for their ability to withstand harsh thermal cycles, erosion resistance (ASTM G76 83 "Standard Practice for Conducting Erosion Tests by Solid Particle Impingement Using Gas Jets") using Al2O3, and adhesion to the graphite fiber polyimide

  16. Responsive Biomaterials: Advances in Materials Based on Shape-Memory Polymers.

    PubMed

    Hardy, John G; Palma, Matteo; Wind, Shalom J; Biggs, Manus J

    2016-07-01

    Shape-memory polymers (SMPs) are morphologically responsive materials with potential for a variety of biomedical applications, particularly as devices for minimally invasive surgery and the delivery of therapeutics and cells for tissue engineering. A brief introduction to SMPs is followed by a discussion of the current progress toward the development of SMP-based biomaterials for clinically relevant biomedical applications. PMID:27120512

  17. 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.

  18. 21 CFR 177.1580 - Polycarbonate resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

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

  19. 21 CFR 177.1580 - Polycarbonate resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

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

  20. 21 CFR 177.1580 - Polycarbonate resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

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

  1. 21 CFR 177.1580 - Polycarbonate resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

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

  2. 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...

  3. 21 CFR 177.1680 - Polyurethane resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

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

  4. 21 CFR 177.1680 - Polyurethane resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

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

  5. 21 CFR 177.1680 - Polyurethane resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

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

  6. 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...

  7. 21 CFR 177.1655 - Polysulfone resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

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

  8. 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...

  9. 21 CFR 177.1380 - Fluorocarbon resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

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

  10. 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...

  11. Thermally conductive polymers

    NASA Technical Reports Server (NTRS)

    Byrd, N. R.; Jenkins, R. K.; Lister, J. L. (Inventor)

    1971-01-01

    A thermally conductive polymer is provided having physical and chemical properties suited to use as a medium for potting electrical components. The polymer is prepared from hydroquinone, phenol, and formaldehyde, by conventional procedures employed for the preparation of phenol-formaldehyde resins. While the proportions of the monomers can be varied, a preferred polymer is formed from the monomers in a 1:1:2.4 molar or ratio of hydroquinone:phenol:formaldehyde.

  12. Fiber-optic Raman spectroscopy for cure monitoring of advanced polymer composites

    SciTech Connect

    Myrick, M.L.; Angel, S.M.; Lyon, R.E.; Vess, T.M.

    1991-12-16

    The curing reaction of an epoxy matrix used for wet filament-wound composites was monitored using Raman spectroscopy measured over fiber optics. The resin system consists of the diglycidyl ether of bisphenol-A in combination with a polyethertriamine hardener in a 1:1 stoichiometric ratio. The extent of chemical reaction of the epoxy as a function of time was measurable through changes in peak heights of several vibrational modes. A Raman peak associated with a phenyl ring vibration in epoxide component was used as in internal reference to correct for density changes and instrumental variations. Temperature measurements were made over the same fiber optics used to obtain the cure chemistry data by measuring the intensity of anti-Stokes Raman scattering from the epoxy. Both single-fiber and dual-fiber probes were evaluated.

  13. Ion-exclusion chromatographic behavior of aliphatic carboxylic acids and benzenecarboxylic acids on a sulfonated styrene--divinylbenzene co-polymer resin column with sulfuric acid containing various alcohols as eluent.

    PubMed

    Ohta, Kazutoku; Towata, Atsuya; Ohashi, Masayoshi

    2003-05-16

    The addition of C1-C7 alcohols (methanol, ethanol, propanol, butanol, heptanol, hexanol and heptanol) to dilute sulfuric acid as eluent in ion-exclusion chromatography using a highly sulfonated styrene-divinylbenzene co-polymer resin (TSKgel SCX) in the H+ form as the stationary phase was carried out for the simultaneous separations of both (a) C1-C7 aliphatic carboxylic acids (formic, acetic, propionic, isobutyric, butyric, isovaleric, valeric, 2-methylvaleric, isocaproic, caproic, 2,2-dimethyl-n-valeric, 2-methylhexanoic, 5-methylhexanoic and heptanoic acids) and (b) benzenecarboxylic acids (pyromellitic, hemimellitic, trimellitic, o-phthalic, m-phthalic, p-phthalic, benzoic and salicylic acids and phenol). Heptanol was the most effective modifier in ion-exclusion chromatography for the improvement of peak shapes and a reduction in retention volumes for higher aliphatic carboxylic acids and benzenecarboxylic acids. Excellent simultaneous separation and relatively highly sensitive conductimetric detection for these C1-C7 aliphatic carboxylic acids were achieved on the TSKgel SCX column (150 x 6 mm I.D.) in 30 min using 0.5 mM sulfuric acid containing 0.025% heptanol as eluent. Excellent simultaneous separation and highly sensitive UV detection at 200 nm for these benzenecarboxylic acids were also achieved on the TSKgel SCX column in 30 min using 5 mM sulfuric acid containing 0.075% heptanol as eluent. PMID:12830881

  14. Ion-exclusion chromatographic separations of C1-C6 aliphatic carboxylic acids on a sulfonated styrene-divinylbenzene co-polymer resin column with 5-methylhexanoic acid as eluent.

    PubMed

    Ohta, Kazutoku; Towata, Atsuya; Ohashi, Masayoshi

    2003-05-16

    The application of C7 aliphatic carboxylic acids (heptanoic, 2-methylhexanoic, 5-methylhexanoic and 2,2-dimethyl-n-valeric acids) as eluents in ion-exclusion chromatography with conductimetric detection for C1-C6 aliphatic carboxylic acids (formic, acetic, propionic, isobutyric, butyric, isovaleric, valeric, isocaproic and caproic acids) was carried out using a highly sulfonated styrene-divinylbenzene co-polymer resin (TSKgel SCX) in the H+ form as a stationary phase. When using 0.05 mM sulfuric acid at pH 4.0 as the eluent, peak shapes of hydrophobic carboxylic acids (isovaleric, valeric, isocaproic and caproic acids) were tailed strongly. In contrast, when using 1 mM these C7 carboxylic acids at pH ca. 4 as the eluents, although system peaks (vacant peaks) corresponding to these C7 carboxylic acids appeared, peak shapes of these hydrophobic acids were improved drastically. Excellent simultaneous separation and relatively high sensitive conductimetric detection for these C1-C6 aliphatic carboxylic acids were achieved in 25 min on the TSKgel SCX column (150 x 6 mm I.D.) using 1 mM 5-methylhexanoic acid at pH 4.0 as the eluent. PMID:12830882

  15. Atom Probe Tomographic Mapping Directly Reveals the Atomic Distribution of Phosphorus in Resin Embedded Ferritin

    PubMed Central

    Perea, Daniel E.; Liu, Jia; Bartrand, Jonah; Dicken, Quinten; Thevuthasan, S. Theva; Browning, Nigel D.; Evans, James E.

    2016-01-01

    Here we report the atomic-scale analysis of biological interfaces within the ferritin protein using atom probe tomography that is facilitated by an advanced specimen preparation approach. Embedding ferritin in an organic polymer resin lacking nitrogen provided chemical contrast to visualise atomic distributions and distinguish the inorganic-organic interface of the ferrihydrite mineral core and protein shell, as well as the organic-organic interface between the ferritin protein shell and embedding resin. In addition, we definitively show the atomic-scale distribution of phosphorus as being at the surface of the ferrihydrite mineral with the distribution of sodium mapped within the protein shell environment with an enhanced distribution at the mineral/protein interface. The sample preparation method is robust and can be directly extended to further enhance the study of biological, organic and inorganic nanomaterials relevant to health, energy or the environment. PMID:26924804

  16. Advanced Compositional Analysis of Nanoparticle-polymer Composites Using Direct Fluorescence Imaging.

    PubMed

    Crick, Colin R; Noimark, Sacha; Peveler, William J; Bear, Joseph C; Ivanov, Aleksandar P; Edel, Joshua B; Parkin, Ivan P

    2016-01-01

    The fabrication of polymer-nanoparticle composites is extremely important in the development of many functional materials. Identifying the precise composition of these materials is essential, especially in the design of surface catalysts, where the surface concentration of the active component determines the activity of the material. Antimicrobial materials which utilize nanoparticles are a particular focus of this technology. Recently swell encapsulation has emerged as a technique for inserting antimicrobial nanoparticles into a host polymer matrix. Swell encapsulation provides the advantage of localizing the incorporation to the external surfaces of materials, which act as the active sites of these materials. However, quantification of this nanoparticle uptake is challenging. Previous studies explore the link between antimicrobial activity and surface concentration of the active component, but this is not directly visualized. Here we show a reliable method to monitor the incorporation of nanoparticles into a polymer host matrix via swell encapsulation. We show that the surface concentration of CdSe/ZnS nanoparticles can be accurately visualized through cross-sectional fluorescence imaging. Using this method, we can quantify the uptake of nanoparticles via swell encapsulation and measure the surface concentration of encapsulated particles, which is key in optimizing the activity of functional materials. PMID:27500449

  17. Recent advances with generalized entropy theory of glass-formation in polymers

    NASA Astrophysics Data System (ADS)

    Freed, Karl

    The generalized entropy theory (GET) of glass-formation in polymers is a combination of the lattice cluster theory (LCT) for the configurational entropy density with the Adam-Gibbs (AG) theory for the structural relaxation time. A greatly simplified form of the GET (whose expression for the free energy is roughly double that of Flory-Huggins theory) accurately reproduces the four characteristic temperatures of glass-formation (the onset, crossover, glass transition, and Kauzmann temperatures) of the full GET to within 4K for a series of models of polymers composed of semi-flexible chains having the structure of poly(n-alpha olefins). The theory is now simple enough to be used in courses in polymer physics. Although the successes of the GET provide a strong validation of the final form of the AG theory provided the configurational entropy is used, the physical basis of the AG theory has remained an enigma. Hence, we have developed a new, more general, statistical mechanical derivation of AG theory that explains the previously perplexing observations that the string-like elementary excitations have the mass and temperature dependence of systems undergoing equilibrium self-assembly. This work is supported by the (U.S.) Department of Energy (DOE), Office of Basic Energy Sciences, Division of Materials Sciences and Engineering under Award No. DE- SC0008631.

  18. Advanced Aromatic Polymers with Excellent Antiatomic Oxygen Performance Derived from Molecular Precursor Strategy and Copolymerization of Polyhedral Oligomeric Silsesquioxane.

    PubMed

    Wang, Pei; Tang, Yusheng; Yu, Zhen; Gu, Junwei; Kong, Jie

    2015-09-16

    In this contribution, the advanced aromatic polymers with excellent antiatomic oxygen (AO) performance were designed and synthesized using molecular precursor strategy and copolymerization of polyhedral oligomeric silsesquioxane (POSS). A soluble poly(p-phenylene benzobisoxazole) (PBO) precursor, that is, TBS-PBO (tert-butyldimethylsilyl was denoted as TBS), was designed to overcome the poor solubility of PBO in organic solvents. Then the new copolymer of TBS-PBO-POSS was synthesized by the copolymerization of TBS-PBO and POSS, which possessed good solubility and film-forming ability in common organic solvents, such as N-methylpyrrolidone, N,N-dimethylacetamide, and dimethyl sulfoxide. More importantly, the TBS-PBO-POSS films exhibited outstanding antiatomic oxygen properties because of the incorporation of POSS monomers with cagelike structure into the main chain of copolymer, which drastically reduced the AO-induced erosion owing to the formation of the passivating silica layer on the surface of polymers. When the TBS-PBO-POSS films were exposed to AO effective fluences of 1.5495×10(20) atom cm(-2) (5 h) and 4.6486×10(20) atom cm(-2) (15 h), the relative mass loss was merely 0.19% and 0.41%, respectively. This work provides a new perspective and efficient strategy for the molecular design of aromatic heterocyclic polymers possessing excellent combination properties including processing convenience and antioxidative and mechanical properties, which can be employed as potential candidates to endure the aggressive environment encountered in low earth orbits. PMID:26322523

  19. Fabrication of Ruthenium Nanoparticles in Porous Organic Polymers: Towards Advanced Heterogeneous Catalytic Nanoreactors.

    PubMed

    Mondal, John; Kundu, Sudipta K; Hung Ng, Wilson Kwok; Singuru, Ramana; Borah, Parijat; Hirao, Hajime; Zhao, Yanli; Bhaumik, Asim

    2015-12-21

    A novel strategy has been adopted for the construction of a copolymer of benzene-benzylamine-1 (BBA-1), which is a porous organic polymer (POP) with a high BET surface area, through Friedel-Crafts alkylation of benzylamine and benzene by using formaldehyde dimethyl acetal as a cross-linker and anhydrous FeCl3 as a promoter. Ruthenium nanoparticles (Ru NPs) were successfully distributed in the interior cavities of polymers through NaBH4, ethylene glycol, and hydrothermal reduction routes, which delivered Ru-A, Ru-B, and Ru-C materials, respectively, and avoided aggregation of metal NPs. Homogeneous dispersion, the nanoconfinement effect of the polymer, and the oxidation state of Ru NPs were verified by employing TEM, energy-dispersive X-ray spectroscopy mapping, cross polarization magic-angle spinning (13)C NMR spectroscopy, and X-ray photoelectron spectroscopy analytical tools. These three new Ru-based POP materials exhibited excellent catalytic performance in the hydrogenation of nitroarenes at RT (with a reaction time of only ≈ 30 min), with high conversion, selectivity, stability, and recyclability for several catalytic cycles, compared with other traditional materials, such as Ru@C, Ru@SiO2, and Ru@TiO2, but no clear agglomeration or loss of catalytic activity was observed. The high catalytic performance of the ruthenium-based POP materials is due to the synergetic effect of nanoconfinement and electron donation offered by the 3D POP network. DFT calculations showed that hydrogenation of nitrobenzene over the Ru (0001) catalyst surface through a direct reaction pathway is more favorable than that through an indirect reaction pathway. PMID:26572500

  20. Photo-Curable Polymer Blend Dielectrics for Advancing Organic Field-Effect Transistor Applications

    SciTech Connect

    S Kim; K Hong; M Jang; J Jang; J Anthony; H Yang; C Park

    2011-12-31

    A solution method of photo-curable and -patternable polymer gate dielectrics was introduced by using blend solutions of poly(4-dimethylsilyl styrene) (PDMSS) and poly(melamine-co-formaldehyde) acrylate (PMFA). The fabrication was optimized to produce a smooth hydrophobic gate dielectric with good insulating and solvent-resistant properties. On the optimized PDMSS/PMFA blend gate dielectric, pentacene could grow into highly ordered structure, showing high electric performances for the resulting OFETs, as well as PTCDI-C13 and TES-ADT.

  1. 21 CFR 175.270 - Poly(vinyl fluoride) resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... polymerization of vinyl fluoride. (b) The poly(vinyl fluoride) basic resins have an intrinsic viscosity of not... Dilute Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference. Copies may be... Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference; see paragraph (b)...

  2. 21 CFR 175.270 - Poly(vinyl fluoride) resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... polymerization of vinyl fluoride. (b) The poly(vinyl fluoride) basic resins have an intrinsic viscosity of not... Dilute Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference. Copies may be... Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference; see paragraph (b)...

  3. 21 CFR 175.270 - Poly(vinyl fluoride) resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... polymerization of vinyl fluoride. (b) The poly(vinyl fluoride) basic resins have an intrinsic viscosity of not... Dilute Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference. Copies may be... Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference; see paragraph (b)...

  4. 21 CFR 175.270 - Poly(vinyl fluoride) resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... polymerization of vinyl fluoride. (b) The poly(vinyl fluoride) basic resins have an intrinsic viscosity of not... Dilute Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference. Copies may be... Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference; see paragraph (b)...

  5. 21 CFR 177.2260 - Filters, resin-bonded.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... of this section. (a) Resin-bonded filters are prepared from natural or synthetic fibers to which have... contain at least 70 weight percent of polymer units derived from ethyl acrylate, no more than 2 weight percent of total polymer units derived from acrylic acid, no more than 10 weight percent of total...

  6. 21 CFR 177.2260 - Filters, resin-bonded.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... of this section. (a) Resin-bonded filters are prepared from natural or synthetic fibers to which have... contain at least 70 weight percent of polymer units derived from ethyl acrylate, no more than 2 weight percent of total polymer units derived from acrylic acid, no more than 10 weight percent of total...

  7. 21 CFR 177.2260 - Filters, resin-bonded.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... of this section. (a) Resin-bonded filters are prepared from natural or synthetic fibers to which have... contain at least 70 weight percent of polymer units derived from ethyl acrylate, no more than 2 weight percent of total polymer units derived from acrylic acid, no more than 10 weight percent of total...

  8. Hot Melt Extruded Amorphous Solid Dispersion of Posaconazole with Improved Bioavailability: Investigating Drug-Polymer Miscibility with Advanced Characterisation

    PubMed Central

    Amin, Purnima

    2014-01-01

    Invasive antifungal infections are reasons for morbidity and mortality in immunogenic patients worldwide. Posaconazole is a most promising antifungal agent against all types of invasive infections with high % of cure rate. The marketed suspension formulation has low bioavailability and is needed to be taken with food. In this paper, PCZ hot melt extruded amorphous solid dispersion (SD) with immediate release and improved bioavailability was prepared using Soluplus (Sol) as primary carrier for solubilization. Surfactants such as PEG 400, Lutrol F27, Lutrol F68, and TPGS are also used in combination with Soluplus to improve the physicochemical performance of the formulation when it comes in contact with GI (gastrointestinal) fluid. Drug-polymer miscibility of SD was investigated using advanced techniques. In the in vivo study, the AUC(0–72) and Cmax of PCZ/Soluplus were 11.5 and 11.74 time higher than those of pure PCZ. The formulation of the extrudate SD had an AUC(0–72) and Cmax higher than those with the commercial capsule (Noxafil). Molecular dynamic (MD) simulation studies were carried out using in silico molecular modelling to understand the drug-polymer intermolecular behaviour. The results of this research ensure enhanced dissolution and bioavailability of the solid dispersion of PCZ prepared by HME compared with the PCZ suspension. PMID:25143935

  9. Engineered glycated amino dendritic polymers as specific nonviral gene delivery vectors targeting the receptor for advanced glycation end products.

    PubMed

    Giron-Gonzalez, M Dolores; Morales-Portillo, Arturo; Salinas-Castillo, Alfonso; Lopez-Jaramillo, F Javier; Hernandez-Mateo, Fernando; Santoyo-Gonzalez, Francisco; Salto-Gonzalez, Rafael

    2014-06-18

    The receptor for advanced glycation end products (RAGE) is involved in diabetes or angiogenesis in tumors. Under pathological conditions, RAGE is overexpressed and upon ligand binding and internalization stimulates signaling pathways that promote cell proliferation. In this work, amino dendritic polymers PEI 25 kDa and alkylated derivatives of PAMAM-G2 were engineered by the nonenzymatic Maillard glycation reaction to generate novel AGE-containing gene delivery vectors targeting the RAGE. The glycated dendritic polymers were easily prepared and retained the capability to bind and protect DNA from endonucleases. Furthermore, while glycation decreased the transfection efficiency of the dendriplexes in CHO-k1 cells which do not express RAGE, glycated dendriplexes acted as efficient transfection reagents in CHO-k1 cells which stably express recombinant RAGE. In addition, preincubation with BSA-AGEs, a natural ligand of the RAGE, or dansyl cadaverine, an inhibitor of the RAGE internalization, blocked transfection, confirming their specificity toward RAGE. The results were confirmed in NRK and RAW264.7 cell lines, which naturally express the receptor. The glycated compounds retain their transfection efficiency in the presence of serum and promote in vivo transfection in a mouse model. Accordingly, RAGE is a suitable molecular target for the development of site-directed engineered glycated nonviral gene vectors. PMID:24852962

  10. Quantum efficiency of PAG decomposition in different polymer matrices at advanced lithographic wavelengths

    NASA Astrophysics Data System (ADS)

    Fedynyshyn, Theodore H.; Sinta, Roger F.; Mowers, William A.; Cabral, Alberto

    2003-06-01

    The Dill ABC parameters for optical resists are typically determined by measuring the change in the intensity of transmitted light at the wavelength of interest as a function of incident energy. The effectiveness of the experiment rests with the fact that the resist optical properties change with exposure and that the optical properties are directly related to the concentration of PAG compound. These conditions are not typically satisfied in CA resists and thus C is unobtainable by this method. FT-IR spectroscopy can directly measure changes in the photoactive species by isolating and measuring absorbance peaks unique to the photoactive species. We employed the ProABC software, specially modified to allow FT-IR absorbance input, to extract ABS parameters through a best fit of the lithography model to experimental data. The quantum efficiency of PAG decomposition at 157-, 193-, and 248-nm was determined for four diazomethane type PAGs in four different polymer matrices. It was found that both the Dill C parameter and the quantum efficiency for all PAGs increased as wavelength decreased, but that the magnitude of the increase was strongly dependent on the polymer matrix.

  11. Novel patternable and conducting metal-polymer nanocomposites: a step towards advanced mutlifunctional materials

    NASA Astrophysics Data System (ADS)

    Rodríguez-Cantó, Pedro J.; Martínez-Marco, Mariluz; Abargues, Rafael; Latorre-Garrido, Victor; Martínez-Pastor, Juan P.

    2013-03-01

    In this work, we present a novel patternable conducting nanocomposite containing gold nanoparticles. Here, the in-situ polymerization of 3T is carried out using HAuCl4 as oxidizing agent inside PMMA as host matrix. During the bake step, the gold salt is also reduced from Au(III) to Au(0) generating Au nanoparticles in the interpenetrating polymer network (IPN) system. We found that this novel multifunctional resist shows electrical conductivity and plasmonic properties as well as potential patterning capability provided by the host matrix. The resulting nanocomposite has been investigated by TEM and UV-Vis spectroscopy. Electrical characterization was also conducted for different concentration of 3T and Au(III) following a characteristic percolation behaviour. Conductivities values from 10-5 to 10 S/cm were successfully obtained depending on the IPN formulation. Moreover, The Au nanoparticles generated exhibited a localized surface plasmon resonance at around 520 nm. This synthetic approach is of potential application to modify the conductivity of numerous insulating polymers and synthesize Au nanoparticles preserving to some extent their physical and chemical properties. In addition, combination of optical properties (Plasmonics), electrical, and lithographic capability in the same material allows for the design of materials with novel functionalities and provides the basis for next generation devices.

  12. Conductive Polymer-Coated VS4 Submicrospheres As Advanced Electrode Materials in Lithium-Ion Batteries.

    PubMed

    Zhou, Yanli; Li, Yanlu; Yang, Jing; Tian, Jian; Xu, Huayun; Yang, Jian; Fan, Weiliu

    2016-07-27

    VS4 as an electrode material in lithium-ion batteries holds intriguing features like high content of sulfur and one-dimensional structure, inspiring the exploration in this field. Herein, VS4 submicrospheres have been synthesized via a simple solvothermal reaction. However, they quickly degrade upon cycling as an anode material in lithium-ion batteries. So, three conductive polymers, polythiophene (PEDOT), polypyrrole (PPY), and polyaniline (PANI), are coated on the surface to improve the electron conductivity, suppress the diffusion of polysulfides, and modify the interface between electrode/electrolyte. PANI is the best in the polymers. It improves the Coulombic efficiency to 86% for the first cycle and keeps the specific capacity at 755 mAh g(-1) after 50 cycles, higher than the cases of naked VS4 (100 mAh g(-1)), VS4@PEDOT (318 mAh g(-1)), and VS4@PPY (448 mAh g(-1)). The good performances could be attributed to the improved charge-transfer kinetics and the strong interaction between PANI and VS4 supported by theoretical simulation. The discharge voltage ∼2.0 V makes them promising cathode materials. PMID:27377263

  13. Support for the Advanced Polymers Beamline at the National Synchrotron Light Source

    SciTech Connect

    Hsiao, Benjamin S

    2008-10-01

    The primary focus of the X27C beamline is to investigate frontier polymer science and engineering problems with emphasis on real-time studies of structures, morphologies and dynamics from atomic, nanoscopic, microscopic to mesoscopic scales using simultaneous small-angle X-ray scattering (SAXS) and wide-angle X-ray diffraction (WAXD) techniques. The scientific merit of this project is as follows. Currently, many unique sample chambers for in-situ synchrotron studies, developed by the PI (B. Hsiao) and Co-PI (B. Chu), are available for general users of X27C at NSLS. These instruments include a gel/melt spinning apparatus, a continuous fiber drawing apparatus, a tensile stretching apparatus, a high pressure X-ray cell using supercritical carbon dioxide, a parallel plate strain-controlled shear stage and a dynamic rheometer for small-strain oscillatory deformation study. Based on the use of these instruments in combination with synchrotron X-rays, many new insights into the relationships between processing and structure have been obtained in recent years. The broader impact of this project is as follows. The X27C beamline is the first synchrotron facility in the United States dedicated to chemistry/materials research (with emphasis on polymers). The major benefit of this facility to the materials community is that no extensive synchrotron experience and equipment preparation are required from general users to carry out cutting-edge experiments.

  14. 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.

  15. Solving the Problem of Building Models of Crosslinked Polymers: An Example Focussing on Validation of the Properties of Crosslinked Epoxy Resins

    PubMed Central

    Hall, Stephen A.; Howlin, Brendan J; Hamerton, Ian; Baidak, Alex; Billaud, Claude; Ward, Steven

    2012-01-01

    The construction of molecular models of crosslinked polymers is an area of some difficulty and considerable interest. We report here a new method of constructing these models and validate the method by modelling three epoxy systems based on the epoxy monomers bisphenol F diglycidyl ether (BFDGE) and triglycidyl-p-amino phenol (TGAP) with the curing agent diamino diphenyl sulphone (DDS). The main emphasis of the work concerns the improvement of the techniques for the molecular simulation of these epoxies and specific attention is paid towards model construction techniques, including automated model building and prediction of glass transition temperatures (Tg). Typical models comprise some 4200–4600 atoms (ca. 120–130 monomers). In a parallel empirical study, these systems have been cast, cured and analysed by dynamic mechanical thermal analysis (DMTA) to measure Tg. Results for the three epoxy systems yield good agreement with experimental Tg ranges of 200–220°C, 270–285°C and 285–290°C with corresponding simulated ranges of 210–230°C, 250–300°C, and 250–300°C respectively. PMID:22916182

  16. Free Radical Addition Polymerization Kinetics without Steady-State Approximations: A Numerical Analysis for the Polymer, Physical, or Advanced Organic Chemistry Course

    ERIC Educational Resources Information Center

    Iler, H. Darrell; Brown, Amber; Landis, Amanda; Schimke, Greg; Peters, George

    2014-01-01

    A numerical analysis of the free radical addition polymerization system is described that provides those teaching polymer, physical, or advanced organic chemistry courses the opportunity to introduce students to numerical methods in the context of a simple but mathematically stiff chemical kinetic system. Numerical analysis can lead students to an…

  17. PMR Resin Compositions For High Temperatures

    NASA Technical Reports Server (NTRS)

    Vannucci, Raymond D.

    1989-01-01

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

  18. 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.

  19. Utilizing advanced polymerization techniques for simplifying polymer grafting from silica colloidal crystal substrates

    NASA Astrophysics Data System (ADS)

    Yerneni, Charu K.

    Polyacrylamide has been well established as a biocompatible material when Polyacrylamide gel electrophoresis (PAGE) came into existence in the 1960s. Under aqueous buffer conditions it becomes non-adsorptive to proteins and due to its molecular level pore forming nature could be used in size based biomolecule separations. Since then considerable research has been done to explore the non-adsorptive nature of polyacrylamide on a platform or substrate. Attempts were made to grow polyacrylamide chains from silica as a substrate which can then be used in various protein separation techniques. Based on an ionic polymerization method which was used for gel casting in PAGE, polymers were grown on silica gel. Though considerable thickness could be achieved, polymerization was not just confined to the surface. Therefore a rigid polymer brush layer could not be achieved. Atom transfer radical polymerization (ATRP) method showed the solution to this problem. Polymer brush layers with acceptable thickness could now be achieved for growing polyacrylamide from silica gel. Yet it still suffered from several disadvantages such as the need of an inert atmosphere for polymerization and limited thickness. Many developments have taken place in the past decade which led to improvements in substrate and polymerization methods. This research used non porous sub-micron silica as the substrate and AGET ATRP (Activator generated electron transfer atom transfer radical polymerization) for surface grafting polyacrylamide. Non porous submicron silica has been shown to be a better stationary phase substrate for protein separations than conventional substrates. AGET ATRP enables polymerization to be performed under ambient conditions and in water based solutions which gives thicknesses much higher than conventional ATRP. Data from various analytical techniques showed that within the experimental range the polymerization is linear and has decent control. This means silica nanoparticles coated with

  20. 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.

  1. Advances in the design of macroporous polymer scaffolds for potential applications in dentistry

    PubMed Central

    Braschler, Thomas M.; Renaud, Philippe

    2013-01-01

    A paradigm shift is taking place in medicine and dentistry from using synthetic implants and tissue grafts to a tissue engineering approach that uses degradable porous three-dimensional (3D) material hydrogels integrated with cells and bioactive factors to regenerate tissues such as dental bone and other oral tissues. Hydrogels have been established as a biomaterial of choice for many years, as they offer diverse properties that make them ideal in regenerative medicine, including dental applications. Being highly biocompatible and similar to native extracellular matrix, hydrogels have emerged as ideal candidates in the design of 3D scaffolds for tissue regeneration and drug delivery applications. However, precise control over hydrogel properties, such as porosity, pore size, and pore interconnectivity, remains a challenge. Traditional techniques for creating conventional crosslinked polymers have demonstrated limited success in the formation of hydrogels with large pore size, thus limiting cellular infiltration, tissue ingrowth, vascularization, and matrix mineralization (in the case of bone) of tissue-engineered constructs. Emerging technologies have demonstrated the ability to control microarchitectural features in hydrogels such as the creation of large pore size, porosity, and pore interconnectivity, thus allowing the creation of engineered hydrogel scaffolds with a structure and function closely mimicking native tissues. In this review, we explore the various technologies available for the preparation of macroporous scaffolds and their potential applications. PMID:24455437

  2. Advanced recognition of explosives in traces on polymer surfaces using LIBS and supervised learning classifiers.

    PubMed

    Serrano, Jorge; Moros, Javier; Sánchez, Carlos; Macías, Jorge; Laserna, J Javier

    2014-01-01

    The large similarity existing in the spectral emissions collected from organic compounds by laser-induced breakdown spectroscopy (LIBS) is a limiting factor for the use of this technology in the real world. Specifically, among the most ambitious challenges of today's LIBS involves the recognition of an organic residue when neglected on the surface of an object of identical nature. Under these circumstances, the development of an efficient algorithm to disclose the minute differences within this highly complex spectral information is crucial for a realistic application of LIBS in countering explosive threats. An approach cemented on scatter plots of characteristic emission features has been developed to identify organic explosives when located on polymeric surfaces (teflon, nylon and polyethylene). By using selected spectral variables, the approach allows to design a concise classifier for alerting when one of four explosives (DNT, TNT, RDX and PETN) is present on the surface of the polymer. Ordinary products (butter, fuel oil, hand cream, olive oil and motor oil) cause no confusion in the decisions taken by the classifier. With rates of false negatives and false positives below 5%, results demonstrate that the classification algorithm enables to label residues according to their harmful nature in the most demanding scenario for a LIBS sensor. PMID:24331046

  3. Advanced treatment of oil recovery wastewater from polymer flooding by UV/H2O2/O3 and fine filtration.

    PubMed

    Guang-Meng, Ren; De-Zhi, Sun; Chunk, Jong Shik

    2006-01-01

    In order to purify oil recovery wastewater from polymer flooding (ORWPF) in tertiary oil recovery in oil fields, advanced treatment of UV/H2O2/O3 and fine filtration were investigated. The experimental results showed that polyacrylamide and oil remaining in ORWPF after the conventional treatment process could be effectively removed by UV/H2O2/O3 process. Fine filtration gave a high performance in eliminating suspended solids. The treated ORWPF can meet the quality requirement of the wastewater-bearing polymer injection in oilfield and be safely re-injected into oil reservoirs for oil recovery. PMID:20050544

  4. Electron Beam Crosslinked Polyurethane Shape Memory Polymers with Tunable Mechanical Properties

    PubMed Central

    Hearon, Keith; Nash, Landon D.; Volk, Brent L.; Ware, Taylor; Lewicki, James P.; Voit, Walter E.; Wilson, Thomas S.

    2014-01-01

    Novel electron beam crosslinked polyurethane shape memory polymers with advanced processing capabilities and tunable thermomechanical properties have been synthesized and characterized. We demonstrate the ability to manipulate crosslink density in order to finely tune rubbery modulus, strain capacity, ultimate tensile strength, recovery stress, and glass transition temperature. This objective is accomplished for the first time in a low-molecular-weight polymer system through the precise engineering of thermoplastic resin precursors suitable for mass thermoplastic processing. Neurovascular stent prototypes were fabricated by dip-coating and laser machining to demonstrate processability. PMID:25411531

  5. Acrylic resin injection method for blood vessel investigations.

    PubMed

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

    2013-01-01

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

  6. Polymer highlights for September 1975

    SciTech Connect

    Hammon, H.G.; Althouse, L.P.; Buckner, A.T.; McKinley, B.; Walkup, C.M.; Rinde, J.; Lorensen, L.L.; Cady, W.E.; Caley, L.E.

    1988-12-15

    Research programs in polymer chemistry are briefly described. The following polymers are under investigation for use as adhesives, nozzles, insulators, or fluid cushions: urethanes, teflon, TFE, Tefzel, Ryton, H Resin, Imidite 2803, PPQ, KELF 800, and KELF 5500. Areas of research application include geothermal and solar energy fields. (CBS)

  7. Polymer-based separations: Synthesis and application of polymers for ionic and molecular recognition

    SciTech Connect

    Alexandratos, S.D.

    1992-01-01

    Polymer-based separations have utilized resins such as sulfonic, acrylic, and iminodiacetic acid resins and the XAD series. Selective polymeric reagents for reaction with a targeted metal ion were synthesized as polymers with two different types of functional groups, each operating on the ions through a different mechanism. There are 3 classes of DMBPs (dual mechanism bifunctional polymers). Research during this period dealing with metal ion recognition focused on two of these classes (reduction of metal ions to metal; selective complexation).

  8. Chemical resistance of optical plastics and resin for level detectors

    NASA Astrophysics Data System (ADS)

    Omegna, Cicero L.; Fontes Garcia, Jonas; Ramos-Gonzáles, Roddy E.; Barbosa, Luiz C.

    2015-09-01

    A test method was developed to find the ideal optical material that supports the chemical reaction of some fuels. Optical plastics and resin were submerged for long periods of time in reservoirs of ethanol, gasoline, Diesel and biodiesel. The dimensional change and weight change of the submerged samples was measured. A special resin successfully supported the chemical attack of fuels. Samples of acrylic polymer and polycarbonate were used as type of optical plastic.

  9. Polymer infiltration studies

    NASA Technical Reports Server (NTRS)

    Marchello, Joseph M.

    1993-01-01

    During the past three months, significant progress has been made on the preparation of carbon fiber composites using advanced polymer resins. The results are set forth in recent reports and publications, and will be presented at forthcoming national and international meetings. Current and ongoing research activities reported herein include: textile composites from powder-coated towpreg; role of surface coating in braiding; prepregger hot sled operation; ribbonizing powder-impregenated towpreg; textile composites from powder-coated towpreg; role of bulk factor powder curtain prepreg process advanced tow placement (ATP) open-section part warpage control. During the coming months research will be directed toward further development of the new powder curtain prepregging method and on ways to customize dry powder towpreg for textile and robotic applications in aircraft part fabrication. Studies of multi-tow powder prepregging and ribbon preparation will be conducted in conjunction with continued development of prepregging technology and the various aspects of composite part fabrication using customized towpreg. Also, during the period ahead work will continue on the analysis of the performance of the new solution prepregger.

  10. Electrically conducting polymers for aerospace applications

    NASA Technical Reports Server (NTRS)

    Meador, Mary Ann B.; Gaier, James R.; Good, Brian S.; Sharp, G. R.; Meador, Michael A.

    1991-01-01

    Current research on electrically conducting polymers from 1974 to the present is reviewed focusing on the development of materials for aeronautic and space applications. Problems discussed include extended pi-systems, pyrolytic polymers, charge-transfer systems, conductive matrix resins for composite materials, and prospects for the use of conducting polymers in space photovoltaics.

  11. Isothermal aging effects on PMR-15 resin

    NASA Technical Reports Server (NTRS)

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

    1992-01-01

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

  12. Advanced nitrogen removal via nitrite using stored polymers in a modified sequencing batch reactor treating landfill leachate.

    PubMed

    Miao, Lei; Wang, Shuying; Li, Baikun; Cao, Tianhao; Xue, Tonglai; Peng, Yongzhen

    2015-09-01

    A modified sequencing batch reactor (SBR) operated at the anaerobic-aerobic-anoxic mode was developed in this study to fully utilize the organics in landfill leachate (ammonia concentration of 1000 ± 50 mg N/L and COD/total nitrogen (TN) ratio of 1-4). The unique feature of modified SBR process was the addition of an anaerobic stage after feeding stage, so that microorganisms could store the organics during anaerobic stage and supply the carbon source for endogenous denitritation after aeration stage. The 70-day operational tests showed the effluent TN was below 10 mg N/L at C/N ratio of 4. The intracellular stored polymers were analyzed and the microorganisms were capable of storing the carbon source as polyhydroxybutyrate (PHB) and glycogen in anaerobic stage, which were the electron donors for endogenous denitritation. Fluorescence in situ hybridization (FISH) analysis showed that glycogen accumulating organisms (GAOs) account for 39.8% of microorganisms in SBR, and carried out advanced nitrogen removal. PMID:26056776

  13. Water transport into epoxy resins and composites

    SciTech Connect

    Tsou, H.S.

    1987-01-01

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

  14. Star Polymers.

    PubMed

    Ren, Jing M; McKenzie, Thomas G; Fu, Qiang; Wong, Edgar H H; Xu, Jiangtao; An, Zesheng; Shanmugam, Sivaprakash; Davis, Thomas P; Boyer, Cyrille; Qiao, Greg G

    2016-06-22

    Recent advances in controlled/living polymerization techniques and highly efficient coupling chemistries have enabled the facile synthesis of complex polymer architectures with controlled dimensions and functionality. As an example, star polymers consist of many linear polymers fused at a central point with a large number of chain end functionalities. Owing to this exclusive structure, star polymers exhibit some remarkable characteristics and properties unattainable by simple linear polymers. Hence, they constitute a unique class of technologically important nanomaterials that have been utilized or are currently under audition for many applications in life sciences and nanotechnologies. This article first provides a comprehensive summary of synthetic strategies towards star polymers, then reviews the latest developments in the synthesis and characterization methods of star macromolecules, and lastly outlines emerging applications and current commercial use of star-shaped polymers. The aim of this work is to promote star polymer research, generate new avenues of scientific investigation, and provide contemporary perspectives on chemical innovation that may expedite the commercialization of new star nanomaterials. We envision in the not-too-distant future star polymers will play an increasingly important role in materials science and nanotechnology in both academic and industrial settings. PMID:27299693

  15. Advanced fiber/matrix material systems

    NASA Technical Reports Server (NTRS)

    Hartness, J. Timothy

    1991-01-01

    Work completed in Phase 1 of the NASA Advanced Composite Technology program is discussed. Two towpreg forms (commingled yarns and fused powder towpregs) are being characterized under the program. These towpregs will be used to evaluate textile fabrication technologies for advanced aircraft composite structures. The unique characteristic of both of these material forms is that both fiber and matrix resin are handled in a single operation such as weaving, braiding, or fiber placement. The evaluation of both commingled and fused powder towpreg is described. Various polymer materials are considered for both subsonic and supersonic applications. Polymers initially being evaluated include thermoplastic polyimides such as Larc-TPI and New-TPI, thermoplastics such as PEEK and PEKEKK as well as some toughened crosslinked polyimides. Preliminary mechanical properties as well as tow handling are evaluated.

  16. Development and characteristics of polymer monoliths for advanced LC bioscreening applications: A review.

    PubMed

    Acquah, Caleb; Moy, Charles K S; Danquah, Michael K; Ongkudon, Clarence M

    2016-03-15

    Biomedical research advances over the past two decades in bioseparation science and engineering have led to the development of new adsorbent systems called monoliths, mostly as stationary supports for liquid chromatography (LC) applications. They are acknowledged to offer better mass transfer hydrodynamics than their particulate counterparts. Also, their architectural and morphological traits can be tailored in situ to meet the hydrodynamic size of molecules which include proteins, pDNA, cells and viral targets. This has enabled their development for a plethora of enhanced bioscreening applications including biosensing, biomolecular purification, concentration and separation, achieved through the introduction of specific functional moieties or ligands (such as triethylamine, N,N-dimethyl-N-dodecylamine, antibodies, enzymes and aptamers) into the molecular architecture of monoliths. Notwithstanding, the application of monoliths presents major material and bioprocess challenges. The relationship between in-process polymerisation characteristics and the physicochemical properties of monolith is critical to optimise chromatographic performance. There is also a need to develop theoretical models for non-invasive analyses and predictions. This review article therefore discusses in-process analytical conditions, functionalisation chemistries and ligands relevant to establish the characteristics of monoliths in order to facilitate a wide range of enhanced bioscreening applications. It gives emphasis to the development of functional polymethacrylate monoliths for microfluidic and preparative scale bio-applications. PMID:26919447

  17. Interpenetrating polymer network approach to tougher and more microcracking resistant high temperature polymers. I - LaRC-RP40

    NASA Technical Reports Server (NTRS)

    Pater, Ruth H.; Morgan, Cassandra D.

    1988-01-01

    Interpenetrating polymer networks in the form of the LaRC-RP40 resin, prepared by the in situ polymerization of a thermosetting imide prepolymer and thermoplastic monomer reactants, are presently used to obtain toughness and microcracking resistance in a high-temperature polymer. Attention is presently given to the processing, physical, and mechanical properties, as well as the thermooxidative stability, of both the neat resin and the resin as a graphite fiber-reinforced matrix. Microcracking after thermal cycling was also tested. LaRC-RP40 exhibits significant resin fracture toughness improvements over the PMR-15 high-temperature matrix resin.

  18. Westinghouse Modular Grinding Process - Enhancement of Volume Reduction for Hot Resin Supercompaction - 13491

    SciTech Connect

    Fehrmann, Henning; Aign, Joerg

    2013-07-01

    In nuclear power plants (NPP) ion exchange (IX) resins are used in several systems for water treatment. Spent resins can contain a significant amount of contaminates which makes treatment for disposal of spent resins mandatory. Several treatment processes are available such as direct immobilization with technologies like cementation, bitumisation, polymer solidification or usage of a high integrity container (HIC). These technologies usually come with a significant increase in final waste volume. The Hot Resin Supercompaction (HRSC) is a thermal treatment process which reduces the resin waste volume significantly. For a mixture of powdered and bead resins the HRSC process has demonstrated a volume reduction of up to 75 % [1]. For bead resins only the HRSC process is challenging because the bead resins compaction properties are unfavorable. The bead resin material does not form a solid block after compaction and shows a high spring back effect. The volume reduction of bead resins is not as good as for the mixture described in [1]. The compaction properties of bead resin waste can be significantly improved by grinding the beads to powder. The grinding also eliminates the need for a powder additive.Westinghouse has developed a modular grinding process to grind the bead resin to powder. The developed process requires no circulation of resins and enables a selective adjustment of particle size and distribution to achieve optimal results in the HRSC or in any other following process. A special grinding tool setup is use to minimize maintenance and radiation exposure to personnel. (authors)

  19. Advances in the engineering science of immiscible polymer blends: A powder route for delicate polymer precursors and a highly renewable polyamide/terephthalate blend system

    NASA Astrophysics Data System (ADS)

    Giancola, Giorgiana

    Powder processing of thermoplastic polymer composites is an effective way to achieve a high level of component homogenization in raw blends prior to melt processing, thus reducing the thermal and shear stress on the components. Polymer blends can be prepared that would otherwise not be possible due to thermodynamic incompatibility. Evaluation of this concept was conducted by processing PMMA and HDPE micron sized powders which were characterized using DSC and rheology. Optical microscopy and SEM, showed that high-quality, fine domain sized blends can be made by the compression molding process. Silica marker spheres were used to qualitatively assess the level dispersive mixing. EDS chemical analysis was effective in providing image contrast between PMMA and HDPE based on the carbonyl and ester oxygen. EDS image maps, combined with secondary electron images show that compression molding of blended powder precursors produces composites of comparable homogeneity and domain size as extrusion processing. FTIR proved valuable when assessing the intimacy of the constituents at the interface of the immiscible domains. The formation of an in-situ, PMMA nano-network structure resulting from solvent extraction and redeposition using DMF was uniquely found on the surface of these immiscible polymer blends. This work has shown that powder processing of polymers is an effective means to melt processed fragile polymers to high quality blends. Recently, efforts towards the development of sustainable materials have evolved due in part to the increase in price and limited supply of crude oil. Immiscible polymer blending is a paradigm that enables synergistic material performance in certain instances where the composite properties are superior to the sum of the constituents. The addition of PA6,10 to PTT offers an opportunity to increase the bio-based content of PTT while simultaneously maintaining or improving mechanical properties. PA6,10 and PTT are immiscible polymers that can be

  20. Development and characterization of soy-based epoxy resins and pultruded FRP composites

    NASA Astrophysics Data System (ADS)

    Zhu, Jiang

    This dissertation focuses on the development, manufacture and characterization of novel soy-based epoxy FRP composites. Use of alternative epoxy resin systems derived from a renewable resource holds potential for low cost raw materials for the polymer and composite industries. Epoxidized Allyl Soyate (EAS) and Epoxidized Methyl Soyate (EMS) were developed from soybean oil with two chemical modification procedures: transesterification and epoxidation. This research investigates the curing characteristics and thermal and mechanical properties of the neat soyate resin systems. The derived soyate resins have higher reactivity and superior performance compared to commercially available epoxidized soybean oil. An efficient two-step curing method was developed in order to utilize these soyate resins to their full potential. The epoxy co-resin systems with varied soyate resin content were successfully used to fabricate composite material through pultrusion. The pultrusion resin systems with 30 wt% soyate resins yielded improved, or comparable mechanical properties with neat commercial resins. A finite element analysis of the heat transfer and curing process was performed to study the processing characterization on glass/epoxy composite pultrusion. This model can be used to establish baseline process variables and will benefit subsequent optimization. This research demonstrates that soy-based resins, especially EAS, show considerable promise as an epoxy resin supplement for use in polymer and composite structural applications. The new products derived from soybean oil can provide competitive performance, low cost and environmental advantages.

  1. Low-Cost Manufacturing of High- Temperature Polymer Composites

    NASA Technical Reports Server (NTRS)

    Sutter, James K.

    1998-01-01

    Major goals of NASA and the Integrated High Performance Turbine Engine Technology (IHPTET) initiative include improvements in the affordability of propulsion systems, significant increases in the thrust/weight ratio, and increases in the temperature capability of components of gas turbine engines. Members of NASA Lewis Research Center's HITEMP project worked cooperatively with Allison Advanced Development Corporation to develop a manufacturing method to produce low-cost components for gas turbine engines. Affordability for these polymer composites is defined by the savings in acquisition and life-cycle costs associated with engine weight reduction. To lower engine component costs, the Lewis/Allison team focused on chopped graphite fiber/polyimide resin composites. The high-temperature polyimide resin chosen, PMR-II-50, was developed at NASA Lewis.

  2. 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)

  3. Methacrylic resin having a high solar radiant energy absorbing property and process for producing the same

    SciTech Connect

    Abe, K.; Kamada, K.; Nakai, Y.

    1981-10-20

    A methacrylic resin having a high solar radiant energy absorbing property wherein an organic compound (A) containing cupric ion and a compound (B) having at least one p-o-h bond in a molecule are contained into the methacrylic resin selected from poly(Methyl methacrylate) or methacrylic polymers containing at least 50% by weight of a methyl methacrylate unit. A process for producing said methacrylic resin is also disclosed.

  4. Preparation of Epoxy Resin Thin Film by Electroless Deposition Method

    NASA Astrophysics Data System (ADS)

    Fukui, Hitoshi; Hirai, Makoto; Shinagawa, Tsutomu; Kobayashi, Yasuyuki; Chigane, Masaya; Fujiwara, Yutaka; Fujita, Naoyuki

    The electrodeposition coating process, which is a polymer film deposition method using water electrolysis, is widely used for automobile body primers. Recently this process is being used in the insulating polymer films deposition for the microelectromechanical system (MEMS) or micro electric components. However, this process has difficulty in depositing polymer film on complex shapes and non-conductive surfaces. In this paper, we demonstrate that epoxy resin thin films used extensively as insulating polymer films were successfully deposited using the electroless chemical reaction in aqueous solution on a non-conductive surface and high aspect glass tube. The substrates catalyzed using a commercialized three-step Sn/Ag/Pd activation process were immersed in the reaction solution containing water-soluble resin and NO3- ion, reducing agent (DMAB). The pH near the substrate rose when NO3- was reduced by released electrons from DMAB. Water-soluble resin combined with OH- hence, polymer thin film was deposited by the electroless deposition reaction. By FE-SEM and FT-IR measurement, it was clear that the conformal and dense epoxy resin films were deposited. Using the present method, epoxy films could be deposited on the surface of a high aspect ratio glass tube 50 mm in length and φ3 in inner diameter. These films had high insulation resistivity of 108∼1011Ωm with applied voltage of 250 V.

  5. Removal of perfluorooctane sulfonate from wastewater by anion exchange resins: effects of resin properties and solution chemistry.

    PubMed

    Deng, Shubo; Yu, Qiang; Huang, Jun; Yu, Gang

    2010-10-01

    Perfluorooctane sulfonate (PFOS) is a new persistent organic pollutant of substantial environmental concern, and its removal from industrial wastewater is critical to eliminate its release into water environment. In this paper, six anion exchange resins with different polymer matrix, porosity, and functional group were evaluated for PFOS removal from simulated wastewater. Resin matrix displayed significant effect on the sorption kinetics and capacity of PFOS, and the polyacrylic resins including IRA67 and IRA958 exhibited faster sorption and higher sorption capacity for PFOS than the polystyrene resins due to the hydrophilic matrix. Sorption isotherms illustrated that the sorption capacity of PFOS on IRA67 and IRA958 was up to 4-5 mmol/g, and the amount of PFOS sorbed on the resins was more than chloride released from resins, indicating that other interactions besides anion exchange were involved in the sorption. Solution pH had little impact on the sorption of PFOS on IRA958, but displayed significant effect on IRA67 at pH above 10 due to the deprotonation of amine groups. The coexisting sulfate and hexavalent chromium in wastewater interfered with the sorption of PFOS because of their competitive sorption on the exchange sites. The spent resins were successfully regenerated using the mixture of NaCl and methanol solution. This work provided an understanding of sorption behavior and mechanism of PFOS on different anion exchange resins, and should result in more effective applications of ion exchange for PFOS removal from industrial wastewater. PMID:20605036

  6. 40 CFR Appendix B to Subpart Nnn... - Free Formaldehyde Analysis of Insulation Resins by Hydroxylamine Hydrochloride

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... in the polymeric form. The hydrolysis of these polymers is catalyzed by hydrogen ions. 2.2The resin... hydroxylamine hydrochloride will produce sufficient hydrogen ions to catalyze the depolymerization of...

  7. INDUSTRIAL PROCESS PROFILES FOR ENVIRONMENTAL USE. CHAPTER 10. THE PLASTICS AND RESINS PRODUCTION INDUSTRY

    EPA Science Inventory

    The report presents a detailed analysis of the plastics and resins production industry, which includes operations that convert industrial organic chemicals into solid or liquid polymers. Elements of the analysis include an industry definition, raw materials, products and manufact...

  8. High energy electron beam curing of epoxy resin systems incorporating cationic photoinitiators

    DOEpatents

    Janke, C.J.; Lopata, V.J.; Havens, S.J.; Dorsey, G.F.; Moulton, R.J.

    1999-03-02

    A mixture of epoxy resins such as a semi-solid triglycidyl ether of tris (hydroxyphenyl) methane and a low viscosity bisphenol A glycidyl ether and a cationic photoinitiator such as a diaryliodonium salt is cured by irradiating with a dosage of electron beams from about 50 to about 150 kGy, forming a cross-linked epoxy resin polymer.

  9. High energy electron beam curing of epoxy resin systems incorporating cationic photoinitiators

    DOEpatents

    Janke, Christopher J.; Lopata, Vincent J.; Havens, Stephen J.; Dorsey, George F.; Moulton, Richard J.

    1999-01-01

    A mixture of epoxy resins such as a semi-solid triglycidyl ether of tris (hydroxyphenyl) methane and a low viscosity bisphenol A glycidyl ether and a cationic photoinitiator such as a diaryliodonium salt is cured by irradiating with a dosage of electron beams from about 50 to about 150 kGy, forming a cross-linked epoxy resin polymer.

  10. Thermal Expansion and Swelling of Cured Epoxy Resin Used in Graphite/Epoxy Composite

    NASA Technical Reports Server (NTRS)

    Adamson, M. J.

    1979-01-01

    The thermal expansion and swelling of resin material as influenced by variations in temperature during moisture absorption is discussed. Comparison measurements using composites constructed of graphite fibers and each of two epoxy resin matrices are included. Polymer theory relative to these findings is discussed and modifications are proposed.

  11. 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.

  12. 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

  13. Scaling law for the dissolution of phenolic resins in aqueous base

    NASA Astrophysics Data System (ADS)

    Yeh, Tung-Feng; Reiser, Arnost; Dammel, Ralph R.; Pawlowski, Georg; Roeschert, Horst

    1993-09-01

    A scaling law derived from percolation theory for the dissolution of phenolic resins in aqueous base is tested and confirmed on seven groups of amphiphilic resins. The scaling law can be presented in the dimensionless form: log(R/R1) equals 2 log[(p - pc)/(1 - pc)]. Here R and R1 are the dissolution rates of the resin and of a standard resin for which p equals 1, the percolation parameter, p, linked to the concentration of hydrophilic sites (OH-groups) in the material, and pc is the percolation threshold below which dissolution no longer occurs. In the group of resins of this study Pc equals 0.20. In its dimensionless form the scaling law provides a single function which applies to all resins of this study and, we believe, to amphiphilic resins in general. This allows the prediction of dissolution rates and the selection of polymer structures which are likely to have specified dissolution kinetics.

  14. Synthesis of Unsaturated Polyester Resins from Various Bio-Derived Platform Molecules.

    PubMed

    Farmer, Thomas J; Castle, Rachael L; Clark, James H; Macquarrie, Duncan J

    2015-01-01

    Utilisation of bio-derived platform molecules in polymer synthesis has advantages which are, broadly, twofold; to digress from crude oil dependence of the polymer industry and secondly to reduce the environmental impact of the polymer synthesis through the inherent functionality of the bio-derived platform molecules. Bulk polymerisation of bio-derived unsaturated di-acids has been employed to produce unsaturated polyester (UPEs) which have been analysed by GPC, TGA, DSC and NMR spectroscopy, advancing on the analysis previously reported. UPEs from the diesters of itaconic, succinic, and fumaric acids were successfully synthesised with various diols and polyols to afford resins of MN 480-477,000 and Tg of -30.1 to -16.6 °C with solubilities differing based on starting monomers. This range of properties allows for many applications and importantly due to the surviving Michael acceptor moieties, solubility and cross-linking can be specifically tailored, post polymerisation, to the desired function. An improved synthesis of itaconate and succinate co-polymers, via the initial formation of an itaconate bis-diol, is also demonstrated for the first time, resulting in significantly improved itaconate incorporation. PMID:26147423

  15. Synthesis of Unsaturated Polyester Resins from Various Bio-Derived Platform Molecules

    PubMed Central

    Farmer, Thomas J.; Castle, Rachael L.; Clark, James H.; Macquarrie, Duncan J.

    2015-01-01

    Utilisation of bio-derived platform molecules in polymer synthesis has advantages which are, broadly, twofold; to digress from crude oil dependence of the polymer industry and secondly to reduce the environmental impact of the polymer synthesis through the inherent functionality of the bio-derived platform molecules. Bulk polymerisation of bio-derived unsaturated di-acids has been employed to produce unsaturated polyester (UPEs) which have been analysed by GPC, TGA, DSC and NMR spectroscopy, advancing on the analysis previously reported. UPEs from the diesters of itaconic, succinic, and fumaric acids were successfully synthesised with various diols and polyols to afford resins of MN 480–477,000 and Tg of −30.1 to −16.6 °C with solubilities differing based on starting monomers. This range of properties allows for many applications and importantly due to the surviving Michael acceptor moieties, solubility and cross-linking can be specifically tailored, post polymerisation, to the desired function. An improved synthesis of itaconate and succinate co-polymers, via the initial formation of an itaconate bis-diol, is also demonstrated for the first time, resulting in significantly improved itaconate incorporation. PMID:26147423

  16. Triclosan antimicrobial polymers

    PubMed Central

    Petersen, Richard C.

    2016-01-01

    Triclosan antimicrobial molecular fluctuating energies of nonbonding electron pairs for the oxygen atom by ether bond rotations are reviewed with conformational computational chemistry analyses. Subsequent understanding of triclosan alternating ether bond rotations is able to help explain several material properties in Polymer Science. Unique bond rotation entanglements between triclosan and the polymer chains increase both the mechanical properties of polymer toughness and strength that are enhanced even better through secondary bonding relationships. Further, polymer blend compatibilization is considered due to similar molecular relationships and polarities. With compatibilization of triclosan in polymers a more uniform stability for nonpolar triclosan in the polymer solid state is retained by the antimicrobial for extremely low release with minimum solubility into aqueous solution. As a result, triclosan is projected for long extended lifetimes as an antimicrobial polymer additive. Further, triclosan rapid alternating ether bond rotations disrupt secondary bonding between chain monomers in the resin state to reduce viscosity and enhance polymer blending. Thus, triclosan is considered for a polymer additive with multiple properties to be an antimicrobial with additional benefits as a nonpolar toughening agent and a hydrophobic wetting agent. The triclosan material relationships with alternating ether bond rotations are described through a complete different form of medium by comparisons with known antimicrobial properties that upset bacterial cell membranes through rapid fluctuating mechanomolecular energies. Also, triclosan bond entanglements with secondary bonding can produce structural defects in weak bacterial lipid membranes requiring pliability that can then interfere with cell division. Regarding applications with polymers, triclosan can be incorporated by mixing into a resin system before cure, melt mixed with thermoplastic polymers that set on cooling

  17. Characterization of Composite Fan Case Resins

    NASA Technical Reports Server (NTRS)

    Dvoracek, Charlene M.

    2004-01-01

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

  18. 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

  19. 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.

  20. Ceramic matrix and resin matrix composites: A comparison

    NASA Technical Reports Server (NTRS)

    Hurwitz, Frances I.

    1987-01-01

    The underlying theory of continuous fiber reinforcement of ceramic matrix and resin matrix composites, their fabrication, microstructure, physical and mechanical properties are contrasted. The growing use of organometallic polymers as precursors to ceramic matrices is discussed as a means of providing low temperature processing capability without the fiber degradation encountered with more conventional ceramic processing techniques. Examples of ceramic matrix composites derived from particulate-filled, high char yield polymers and silsesquioxane precursors are provided.

  1. Ceramic matrix and resin matrix composites - A comparison

    NASA Technical Reports Server (NTRS)

    Hurwitz, Frances I.

    1987-01-01

    The underlying theory of continuous fiber reinforcement of ceramic matrix and resin matrix composites, their fabrication, microstructure, physical and mechanical properties are contrasted. The growing use of organometallic polymers as precursors to ceramic matrices is discussed as a means of providing low temperature processing capability without the fiber degradation encountered with more conventional ceramic processing techniques. Examples of ceramic matrix composites derived from particulate-filled, high char yield polymers and silsesquioxane precursors are provided.

  2. 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.

  3. Advanced analysis of polymer emulsions: Particle size and particle size distribution by field-flow fractionation and dynamic light scattering.

    PubMed

    Makan, Ashwell C; Spallek, Markus J; du Toit, Madeleine; Klein, Thorsten; Pasch, Harald

    2016-04-15

    Field flow fractionation (FFF) is an advanced fractionation technique for the analyses of very sensitive particles. In this study, different FFF techniques were used for the fractionation and analysis of polymer emulsions/latexes. As model systems, a pure acrylic emulsion and emulsions containing titanium dioxide were prepared and analyzed. An acrylic emulsion polymerization was conducted, continuously sampled from the reactor and subsequently analyzed to determine the particle size, radius of gyration in specific, of the latex particles throughout the polymerization reaction. Asymmetrical flow field-flow fractionation (AF4) and sedimentation field-flow fractionation (SdFFF), coupled to a multidetector system, multi-angle laser light scattering (MALLS), ultraviolet (UV) and refractive index (RI), respectively, were used to investigate the evolution of particle sizes and particle size distributions (PSDs) as the polymerization progressed. The obtained particle sizes were compared against batch-mode dynamic light scattering (DLS). Results indicated differences between AF4 and DLS results due to DLS taking hydration layers into account, whereas both AF4 and SdFFF were coupled to MALLS detection, hence not taking the hydration layer into account for size determination. SdFFF has additional separation capabilities with a much higher resolution compared to AF4. The calculated radii values were 5 nm larger for SdFFF measurements for each analyzed sample against the corresponding AF4 values. Additionally a low particle size shoulder was observed for SdFFF indicating bimodality in the reactor very early during the polymerization reaction. Furthermore, different emulsions were mixed with inorganic species used as additives in cosmetics and coatings such as TiO2. These complex mixtures of species were analyzed to investigate the retention and particle interaction behavior under different AF4 experimental conditions, such as the mobile phase. The AF4 system was coupled online

  4. 21 CFR 173.10 - Modified polyacrylamide resin.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Modified polyacrylamide resin. 173.10 Section 173.10 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) SECONDARY DIRECT FOOD ADDITIVES PERMITTED IN FOOD FOR HUMAN CONSUMPTION Polymer Substances and...

  5. 21 CFR 177.2430 - Polyether resins, chlorinated.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyether resins, chlorinated. 177.2430 Section 177.2430 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 Only...

  6. 21 CFR 177.2430 - Polyether resins, chlorinated.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyether resins, chlorinated. 177.2430 Section 177.2430 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...

  7. 21 CFR 177.2500 - Polyphenylene sulfone resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Polyphenylene sulfone resins. 177.2500 Section 177.2500 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 Only...

  8. 21 CFR 177.2500 - Polyphenylene sulfone resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyphenylene sulfone resins. 177.2500 Section 177.2500 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 Only...

  9. 21 CFR 177.2420 - Polyester resins, cross-linked.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Polyester resins, cross-linked. 177.2420 Section 177.2420 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 Only as Components of Articles Intended for...

  10. 21 CFR 177.2420 - Polyester resins, cross-linked.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyester resins, cross-linked. 177.2420 Section 177.2420 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 Only as Components of Articles Intended for...

  11. Process for encapsulating radioactive organic liquids in a resin

    SciTech Connect

    Drake, S.S.; Filter, H.E.

    1983-05-03

    Radioactive organic liquids are converted to a form suitable for burial by the process wherein the liquid is contacted with insoluble, swellable polymer particles to form swollen gelled particles which are dispersed in an unsaturated polyester, vinyl ester resin or mixture thereof which is then cured to a solid state with the gelled particles encased therein.

  12. 21 CFR 177.2420 - Polyester resins, cross-linked.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Polyester resins, cross-linked. 177.2420 Section 177.2420 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use Only as Components of Articles Intended for Repeated Use § 177.2420 Polyester...

  13. 21 CFR 177.2260 - Filters, resin-bonded.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Filters, resin-bonded. 177.2260 Section 177.2260 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 Only as Components of Articles Intended for Repeated Use...

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

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Poly(aryletherketone) resins. 177.2415 Section 177.2415 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 Only as Components of Articles Intended for...

  15. From Commodity Polymers to Functional Polymers

    PubMed Central

    Xiang, Tao; Wang, Ling-Ren; Ma, Lang; Han, Zhi-Yuan; Wang, Rui; Cheng, Chong; Xia, Yi; Qin, Hui; Zhao, Chang-Sheng

    2014-01-01

    Functional polymers bear specified chemical groups, and have specified physical, chemical, biological, pharmacological, or other uses. To adjust the properties while keeping material usage low, a method for direct synthesis of functional polymers is indispensable. Here we show that various functional polymers can be synthesized by in situ cross-linked polymerization/copolymerization. We demonstrate that the polymers synthesized by the facile method using different functional monomers own outstanding pH-sensitivity and pH-reversibility, antifouling property, antibacterial, and anticoagulant property. Our study opens a route for the functionalization of commodity polymers, which lead to important advances in polymeric materials applications. PMID:24710333

  16. A New Class Of Bilevel And Mono-Level Positive Resist Systems Based On A Chemically Stable Imide Polymer

    NASA Astrophysics Data System (ADS)

    Legenza, M. W.; Vidusek, D. A.; de Grandpre, M.

    1985-04-01

    A new resin system, comprising a thermoplastic polymer backbone with chemically stable imide functionality, has been adapted for use in three different positive resist product types. These include an advanced bilayer system, a near, mid and deep UV monolevel resist; and an antireflective coating. The key features of the imide polymer system which are utilized for the new resist products are: 1. Novolac-like solubility in aqueous base. This property allows formulation of resists, including the planarizing layer of a bilevel system, with conventional types of positive resist photoactive compounds and aqueous base developers, unlike the situation with PMMA which is not base soluble. 2. Transparency to wavelengths above 260nm. This permits use of the polymer as the matrix for systems which utilize mid and deep UV exposure, including the planarizing layer for a bilevel system and mid and deep UV monolayer resists. This is in contrast to novolac resin wHch absorbs strongly in the deep UV region. 3. Insolubility in solvents used for conventional positive resists. This property is critical to use of the resin in planarizing layers of bilevel systems, including antirefiective coatings. It eliminates the intermixing problems which represent a major problem in conventional PMMA bilevel systems. 4. High Tg (185°C). This value is about 80°C higher than that of PMMA and allows higher temperature processing without pattern distortion. 5. Chemical stability and plasma resistance. Unlike conventional reactive polyimide resins the subject polymer is chemically unreactive and is stable to temperatures above 300°C. Further, the polymer has significantly greater resistance to plasma than does PMMA.

  17. 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.

  18. Review of recent advances in the preparation of organic polymer monoliths for liquid chromatography of large molecules.

    PubMed

    Arrua, R Dario; Talebi, Mohammad; Causon, Tim J; Hilder, Emily F

    2012-08-13

    In recent years the use of monolithic polymers in separation science has greatly increased due to the advantages these materials present over particle-based stationary phases, such as their relative ease of preparation and good permeability. For these reasons, these materials present high potential as stationary phases for the separation and purification of large molecules such as proteins, peptides, nucleic acids and cells. An example of this is the wide range of commercial available polymer-based monolithic columns now present in the market. This review summarizes recent developments in the synthesis of monolithic polymers for separation science, such as the incorporation of nanostructures in the polymeric scaffold as well as the preparation of hybrid structures. The different methods used in the surface functionalization of monolithic columns are also reviewed. Finally, we critically discuss the recent applications of this column technology in the separation of large molecules under different chromatographic mode. PMID:22790694

  19. Development of a Heterogeneous Laminating Resin

    NASA Technical Reports Server (NTRS)

    Gosnell, R.

    1984-01-01

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

  20. A mechanism for enhancing ionic accessibility into selective ion exchange resins

    SciTech Connect

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

    1998-07-01

    A bifunctional monophosphonic/sulfonic acid ion exchange resin with high capacity has been synthesized. Metal ion studies have been carried out with europium, americium, and ferric nitrate in solutions of varying acidity, with and without sodium nitrate added. The bifunctional resin complexes far higher levels of Eu(III) from 0.5 and 1 N nitric acid than the monofunctional phosphonic acid resin. It is postulated that the sulfonic acid ligand provides an access mechanism for the metal ions into the polymer matrix by hydrating the matrix and preventing its collapse in high ionic strength solutions thus allowing for rapid ionic complexation by the selective phosphonic acid ligands. The bifunctional monophosphonic/sulfonic acid resin has both ligands bound to a polystyrene support. It complexes higher levels of metal ions than a comparable resin differing only by having the monophosphonic acid ligand directly bound to the C-C backbone. Results are compared to a diphosphonic/sulfonic acid resin.

  1. Injection repair of carbon fiber/bismaleimide composite panels with bisphenol E cyanate ester resin

    SciTech Connect

    Thunga, Mahendra; Bauer, Amy; Obusek, Kristine; Meilunas, Ray; Akinc, Mufit; Kessler, Michael R

    2014-08-01

    Resin injection of bisphenol E cyanate ester, a low viscosity resin that cures into a high temperature thermoset polymer, is investigated as a reliable repair method to restore strength and stiffness in delaminated carbon fiber/bismaleimide composites used in aircraft panels. The influence of temperature on the viscosity of the uncured resin was measured to optimize the injection conditions for high resin infiltration into the delaminations. The repair efficiency of the resin was evaluated by varying the panel thickness and the method by which the delamination damage was created in the composite specimens. Ultrasonic scanning (C-scan), flash thermography images, and cross-section analysis of repaired panels revealed excellent resin infiltration into the damaged region. Evaluation of mechanical repair efficiency using both bending stiffness and in-plain compressive strength of the composite panels as the repair metrics showed values exceeding 100%.

  2. Processing-property relationships in epoxy resin/titanium dioxide nanocomposites

    SciTech Connect

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

    2010-01-01

    In situ precipitated titanium dioxide nanoparticles improve the physical properties of polymer composites. Since the pioneering work at Toyota Research Center on exfoliated montmorillonite nanoparticles in a nylon matrix, extensive studies have been performed on polymer nanocomposites in an effort to better integrate organic and inorganic phases. Inorganic fillers, such as silicon and titanium oxides, are widely used because of their remarkable enhancement of the mechanical, electrical, barrier, and flame-retardancy properties of organic polymers. The dispersion and size of the fillers determine the performance of nanocomposites and, despite numerous methods and processing conditions reported in the literature, a universally simple method to scale up the distribution of nanofillers remains a challenge. A significant part of our research involves formulation of novel nanodielectrics that can withstand high electric fields and exhibit superior mechanical performance. Focusing on nanocomposites operating at cryogenic temperatures, our group developed an in situ method for nucleating titanium dioxide (TiO{sub 2}) nanoparticles in polyvinyl alcohol. We also applied this method to a variety of polymer matrices. Here, we present our recent work on a cryogenic resin filled with TiO{sub 2} nanoparticles. Using a particle-precursor solution from which TiO{sub 2} precipitates, we nucleated nanoparticles within the cryogenic epoxy resin Araldite 5808 (Huntsman Advanced Materials Inc., USA). We fabricated nanocomposite films at low weight percentages ({approx}2.5%) to avoid formation of large aggregates and interfaces. The morphology and dispersion of the in situ synthesized nanoparticles are shown by low- and high-magnification transmission-electron-microscopy (TEM) images. The TiO{sub 2} particles ({le}5nm in diameter) are uniformly nucleated and form evenly distributed nanometer-sized clusters in the polymer matrix. This morphology differs significantly from nanocomposites

  3. 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.

  4. 21 CFR 173.70 - Chloromethylated aminated styrene-divinylbenzene resin.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... FOOD FOR HUMAN CONSUMPTION Polymer Substances and Polymer Adjuvants for Food Treatment § 173.70... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Chloromethylated aminated styrene-divinylbenzene resin. 173.70 Section 173.70 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND...

  5. 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.

  6. 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.

  7. 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.

  8. Epoxy resin holograms

    NASA Astrophysics Data System (ADS)

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

    2006-02-01

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

  9. Rotationally Molded Liquid Crystalline Polymers

    NASA Technical Reports Server (NTRS)

    Rogers, Martin; Stevenson, Paige; Scribben, Eric; Baird, Donald; Hulcher, Bruce

    2002-01-01

    Rotational molding is a unique process for producing hollow plastic parts. Rotational molding offers advantages of low cost tooling and can produce very large parts with complicated shapes. Products made by rotational molding include water tanks with capacities up to 20,000 gallons, truck bed liners, playground equipment, air ducts, Nylon fuel tanks, pipes, toys, stretchers, kayaks, pallets, and many others. Thermotropic liquid crystalline polymers are an important class of engineering resins employed in a wide variety of applications. Thermotropic liquid crystalline polymers resins are composed of semi-rigid, nearly linear polymeric chains resulting in an ordered mesomorphic phase between the crystalline solid and the isotropic liquid. Ordering of the rigid rod-like polymers in the melt phase yields microfibrous, self-reinforcing polymer structures with outstanding mechanical and thermal properties. Rotational molding of liquid crystalline polymer resins results in high strength and high temperature hollow structures useful in a variety of applications. Various fillers and reinforcements can potentially be added to improve properties of the hollow structures. This paper focuses on the process and properties of rotationally molded liquid crystalline polymers.

  10. Rotationally Molded Liquid Crystalline Polymers

    NASA Technical Reports Server (NTRS)

    Rogers, Martin; Scribben, Eric; Baird, Donald; Hulcher, Bruce

    2002-01-01

    Rotational molding is a unique process for producing hollow plastic parts. Rotational molding offers low cost tooling and can produce very large parts with complicated shapes. Products made by rotational molding include water tanks with capacities up to 20,000 gallons, truck bed liners, playground equipment, air ducts, Nylon fuel tanks, pipes, toys, stretchers, kayaks, pallets, and many others. Thermotropic liquid crystalline polymers are an important class of engineering resins employed in a wide variety of applications. Thermotropic liquid crystalline polymers resins are composed of semirigid, nearly linear polymeric chains resulting in an ordered mesomorphic phase between the crystalline solid and the isotropic liquid. Ordering of the rigid rod-like polymers in the melt phase yields microfibrous, self-reinforcing polymer structures with outstanding mechanical and thermal properties. Rotational molding of liquid crystalline polymer resins results in high strength and high temperature hollow structures useful in a variety of applications. Various fillers and reinforcements can potentially be added to improve properties of the hollow structures. This paper focuses on the process and properties of rotationally molded liquid crystalline polymers. This paper will also highlight the interactions between academia and small businesses in developing new products and processes.

  11. Chemical derivatization to enhance chemical/oxidative stability of resorcinol-formaldehyde resin

    SciTech Connect

    Hubler, T.L.

    1997-10-01

    The goal of this task is to develop modified resorcinol-formaldehyde (R-F) resin to improve the chemical/oxidative stability of the resin. R-F resin is a regenerable organic ion-exchange resin that is selective for cesium ion in highly alkaline, high ionic-strength solutions. R-F resin tends to undergo chemical degradation, reducing its ability to remove cesium ion from waste solutions; the mechanistic details of these decomposition reactions are currently unknown. The approach used for this task is chemical modification of the resin structure, particularly the resorcinol ring unit of the polymer resin. This approach is based on prior characterization studies conducted at Pacific Northwest National Laboratory (PNNL) that indicated the facile chemical degradation of the resin is oxidation of the resorcinol ring to the para-quinone structure, with subsequent loss of ion-exchange sites for cesium ion. R-F resin represents an important alternative to current radiocesium remediation technology for tank wastes at both the Hanford and Savannah River sites, particularly if regenerable resins are needed.

  12. Composition and method for making polyimide resin-reinforced fabric

    NASA Technical Reports Server (NTRS)

    Serafini, T. T.; Delvigs, P. (Inventor)

    1981-01-01

    A composition for making polyimide resin reinforced fibers or fabric is discussed. The composition includes a polyfunctional ester, a polyfunctional amine, and an end capping agent. The composition is impregnated into fibers or fabric and heated to form prepreg material. The tack retention characteristics of this prepreg material are improved by incorporating into the composition a liquid olefinic material compatible with the other ingredients of the composition. The prepreg material is heated at a higher temperature to effect formation of the polyimide resin and the monomeric additive is incorporated in the polyimide polymer structure.

  13. Recent Advances in Gas Barrier Thin Films via Layer-by-Layer Assembly of Polymers and Platelets.

    PubMed

    Priolo, Morgan A; Holder, Kevin M; Guin, Tyler; Grunlan, Jaime C

    2015-05-01

    Layer-by-layer (LbL) assembly has emerged as the leading non-vacuum technology for the fabrication of transparent, super gas barrier films. The super gas barrier performance of LbL deposited films has been demonstrated in numerous studies, with a variety of polyelectrolytes, to rival that of metal and metal oxide-based barrier films. This Feature Article is a mini-review of LbL-based multilayer thin films with a 'nanobrick wall' microstructure comprising polymeric mortar and nano-platelet bricks that impart high gas barrier to otherwise permeable polymer substrates. These transparent, water-based thin films exhibit oxygen transmission rates below 5 × 10(-3) cm(3) m(-2) day(-1) atm(-1) and lower permeability than any other barrier material reported. In an effort to put this technology in the proper context, incumbent technologies such as metallized plastics, metal oxides, and flake-filled polymers are briefly reviewed. PMID:25800245

  14. Renewability is not Enough: Recent Advances in the Sustainable Synthesis of Biomass-Derived Monomers and Polymers.

    PubMed

    Llevot, Audrey; Dannecker, Patrick-Kurt; von Czapiewski, Marc; Over, Lena C; Söyler, Zafer; Meier, Michael A R

    2016-08-01

    Taking advantage of the structural diversity of different biomass resources, recent efforts were directed towards the synthesis of renewable monomers and polymers, either for the substitution of petroleum-based resources or for the design of novel polymers. Not only the use of biomass, but also the development of sustainable chemical approaches is a crucial aspect for the production of sustainable materials. This review discusses the recent examples of chemical modifications and polymerizations of abundant biomass resources with a clear focus on the sustainability of the described processes. Topics such as synthetic methodology, catalysis, and development of new solvent systems or greener alternative reagents are addressed. The chemistry of vegetable oil derivatives, terpenes, lignin, carbohydrates, and sugar-based platform chemicals was selected to highlight the trends in the active field of a sustainable use of renewable resources. PMID:27355829

  15. Functional polymers

    SciTech Connect

    Wegner, G.

    2000-01-01

    Improving the existing polymer materials and the designing of model polymers need fundamental insights into the structure and dynamics over a large range of length and time scales. Consequently, a host of quite different methods needs to be applied to gain insights into the molecular and supramolecular structures and interactions that determine the performance of these materials. Supramolecular structures derived from shape persistent (stiff) macromolecules are used as examples to demonstrate the correlation between chemical structure, order phenomena and performance in applications concerning advanced or developing technologies: organic light emitting diodes (OLEDs) and separator membranes in lithium based batteries and fuel cells. Polymers are also important as additives in the manufacture and the processing of other materials. The design of block copolymers to control the nucleation and growth of inorganic particles precipitating from aqueous solutions (mineralization) is discussed as well as the use of block copolymers to optimize the processing of ceramic pieces and objects. Finally, the modification of surfaces by polymers including aspects of biocompatibility is discussed. Some remarks concerning the importance of recent developments and advances in synthesis of macromolecular materials are also given.

  16. 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.

  17. Novel alkyd-type coating resins produced using cationic polymerization

    SciTech Connect

    Chisholm, Bret J.; Kalita, Harjyoti; Alam, Samim; Jayasooriyamu, Anurad; Fernando, Shashi; Samanata, Satyabrata; Bahr, James; Selvakumar, Sermadurai; Sibi, Mukund; Vold, Jessica; Ulven, Chad

    2015-05-06

    Novel, partially bio-based poly(vinyl ether) copolymers derived from soybean oil and cyclohexyl vinyl ether (CHVE) were produced by cationic polymerization and investigated for application as alkyd-type surface coatings. Compared to conventional alkyd resins, which are produced by high temperature melt condensation polymerization, the poly(v9nyl ether)s provide several advantages. These advantages include milder, more energy efficient polymer synthesis, elimination of issues associated with gelation during polymer synthesis, production of polymers with well-defined composition and relatively narrow molecular weight distribution, and elimination of film formation and physical property issues associated with entrained monomers, dimers, trimers, etc. The results of the studied showed that the thermal, mechanical, and physical properties of the coatings produced from these novel polymers varied considerably as a function of polymer composition and cure temperature. Overall, the results suggest a good potential for these novel copolymers to be used for coatings cured by autoxidation.

  18. Kinetic modelling of vinyl ester resin polymerization

    SciTech Connect

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

    1993-12-31

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

  19. 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.

  20. 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.

  1. Application of mass spectrometry to process control for polymer material in autoclave curing

    NASA Technical Reports Server (NTRS)

    Smith, A. C.

    1983-01-01

    Mass spectrometer analysis of gas samples collected during a cure cycle of polymer materials can be used as a process control technique. This technique is particularly helpful in studying the various types of solvents and resin systems used in the preparation of polymer materials and characterizing the chemical composition of different resin systems and their mechanism of polymerization.

  2. Asphaltenes-based polymer nano-composites

    DOEpatents

    Bowen, III, Daniel E

    2013-12-17

    Inventive composite materials are provided. The composite is preferably a nano-composite, and comprises an asphaltene, or a mixture of asphaltenes, blended with a polymer. The polymer can be any polymer in need of altered properties, including those selected from the group consisting of epoxies, acrylics, urethanes, silicones, cyanoacrylates, vulcanized rubber, phenol-formaldehyde, melamine-formaldehyde, urea-formaldehyde, imides, esters, cyanate esters, allyl resins.

  3. Thermoset polymers via ring opening metathesis polymerization of functionalized oils

    DOEpatents

    Larock, Richard C; Henna, Phillip H; Kessier, Michael R

    2012-11-27

    The invention provides a method for producing a thermosetting resin from renewable oils, the method comprising supplying renewable oil molecules containing strained ring alkene moieties; reacting the alkene moieties with cyclic alkenes to create a polymer; and repeating the above two steps until the resin having desired characteristics are obtained. Also provided is a thermoset resin comprising functionalized renewable oil polymerized with a co-monomer.

  4. Polymer Stamps for Imprinting Nanopatterns in Polymer Substrate.

    PubMed

    Wu, Jiahao; Amirsadeghi, Alborz; Kim, Jinsoo; Park, Sunggook

    2015-01-01

    Using a silicone or metallic stamp for imprinting multiscale patterns comprising micro down to nanoscale patterns into polymer substrates often results in significant deformation in the molded substrate and loss of pattern transfer fidelity for nanopatterns. In the worst case, the expensive stamp can also be damaged. One method to reduce the problem is to use polymer as the stamp material, which will reduce both adhesion and thermal stress generated at the stamp/substrate interface. In this paper, stamps made of three different polymer materials, i.e., polydimethylsiloxane (PDMS), PPGDA-based UV resin and TPGDA-based UV-resin, were fabricated from the same master containing nanofluidic structures and the replication fidelity from the master, polymer stamps, to thermal-imprinted poly(methyl methacrylate) substrate (PMMA) was compared. The largest loss of pattern fidelity occurs in the thermal imprinting step. Polymer stamps with higher Young's moduli result in a better fidelity in pattern transfer. With TPGDA-based UV resin stamps, multiscale structures with a nanochannel with minimum width and height of -70 nm can be imprinted onto PMMA substrate together with macro-scale patterns by a single nanoimprinting processes. PMID:26328384

  5. Electron beam curing of polymer matrix composites

    SciTech Connect

    Janke, C.J.; Wheeler, D.; Saunders, C.

    1998-01-08

    The purpose of the CRADA was to conduct research and development activities to better understand and utilize the electron beam PMC curing technology. This technology will be used to replace or supplement existing PMC thermal curing processes in Department of Energy (DOE) Defense Programs (DP) projects and American aircraft and aerospace industries. This effort involved Lockheed Martin Energy Systems, Inc./Lockheed Martin Energy Research Corp. (Contractor), Sandia National Laboratories, and ten industrial Participants including four major aircraft and aerospace companies, three advanced materials companies, and three electron beam processing organizations. The technical objective of the CRADA was to synthesize and/or modify high performance, electron beam curable materials that meet specific end-use application requirements. There were six tasks in this CRADA including: Electron beam materials development; Electron beam database development; Economic analysis; Low-cost Electron Beam tooling development; Electron beam curing systems integration; and Demonstration articles/prototype structures development. The contractor managed, participated and integrated all the tasks, and optimized the project efforts through the coordination, exchange, and dissemination of information to the project participants. Members of the Contractor team were also the principal inventors on several electron beam related patents and a 1997 R and D 100 Award winner on Electron-Beam-Curable Cationic Epoxy Resins. The CRADA achieved a major breakthrough for the composites industry by having successfully developed high-performance electron beam curable cationic epoxy resins for use in composites, adhesives, tooling compounds, potting compounds, syntactic foams, etc. UCB Chemicals, the world`s largest supplier of radiation-curable polymers, has acquired a license to produce and sell these resins worldwide.

  6. Polymer-Layered Silicate Nanocomposites for Cryotank Applications

    NASA Technical Reports Server (NTRS)

    Miller, Sandi G.; Meador, Michael A.

    2007-01-01

    Previous composite cryotank designs have relied on the use of conventional composite materials to reduce microcracking and permeability. However, revolutionary advances in nanotechnology derived materials may enable the production of ultra-lightweight cryotanks with significantly enhanced durability and damage tolerance, as well as reduced propellant permeability. Layered silicate nanocomposites are especially attractive in cryogenic storage tanks based on results that have been reported for epoxy nanocomposite systems. These materials often exhibit an order of magnitude reduction in gas permeability when compared to the base resin. In addition, polymer-silicate nanocomposites have been shown to yield improved dimensional stability, strength, and toughness. The enhancement in material performance of these systems occurs without property trade-offs which are often observed in conventionally filled polymer composites. Research efforts at NASA Glenn Research Center have led to the development of epoxy-clay nanocomposites with 70% lower hydrogen permeability than the base epoxy resin. Filament wound carbon fiber reinforced tanks made with this nanocomposite had a five-fold lower helium leak rate than the corresponding tanks made without clay. The pronounced reduction observed with the tank may be due to flow induced alignment of the clay layers during processing. Additionally, the nanocomposites showed CTE reductions of up to 30%, as well as a 100% increase in toughness.

  7. Reactivity of Resorcinol Formaldehyde Resin with Nitric Acid

    SciTech Connect

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

    2005-10-25

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

  8. REACTIVITY OF RESORCINOL FORMALDEHYDE RESIN WITH NITRIC ACID

    SciTech Connect

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

    2006-06-14

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

  9. 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.

  10. Nonlinear Inelastic Mechanical Behavior Of Epoxy Resin Polymeric Materials

    NASA Astrophysics Data System (ADS)

    Yekani Fard, Masoud

    Polymer and polymer matrix composites (PMCs) materials are being used extensively in different civil and mechanical engineering applications. The behavior of the epoxy resin polymers under different types of loading conditions has to be understood before the mechanical behavior of Polymer Matrix Composites (PMCs) can be accurately predicted. In many structural applications, PMC structures are subjected to large flexural loadings, examples include repair of structures against earthquake and engine fan cases. Therefore it is important to characterize and model the flexural mechanical behavior of epoxy resin materials. In this thesis, a comprehensive research effort was undertaken combining experiments and theoretical modeling to investigate the mechanical behavior of epoxy resins subject to different loading conditions. Epoxy resin E 863 was tested at different strain rates. Samples with dog-bone geometry were used in the tension tests. Small sized cubic, prismatic, and cylindrical samples were used in compression tests. Flexural tests were conducted on samples with different sizes and loading conditions. Strains were measured using the digital image correlation (DIC) technique, extensometers, strain gauges, and actuators. Effects of triaxiality state of stress were studied. Cubic, prismatic, and cylindrical compression samples undergo stress drop at yield, but it was found that only cubic samples experience strain hardening before failure. Characteristic points of tensile and compressive stress strain relation and load deflection curve in flexure were measured and their variations with strain rate studied. Two different stress strain models were used to investigate the effect of out-of-plane loading on the uniaxial stress strain response of the epoxy resin material. The first model is a strain softening with plastic flow for tension and compression. The influence of softening localization on material behavior was investigated using the DIC system. It was found that

  11. Polymer-based separations: Synthesis and application of polymers for ionic and molecular recognition. Triennial performance report, August 1, 1989--July 31, 1992

    SciTech Connect

    Alexandratos, S.D.

    1992-01-01

    Polymer-based separations have utilized resins such as sulfonic, acrylic, and iminodiacetic acid resins and the XAD series. Selective polymeric reagents for reaction with a targeted metal ion were synthesized as polymers with two different types of functional groups, each operating on the ions through a different mechanism. There are 3 classes of DMBPs (dual mechanism bifunctional polymers). Research during this period dealing with metal ion recognition focused on two of these classes (reduction of metal ions to metal; selective complexation).

  12. Plastic deformation mechanisms in polyimide resins and their semi-interpenetrating networks

    NASA Technical Reports Server (NTRS)

    Jang, Bor Z.

    1990-01-01

    High-performance thermoset resins and composites are critical to the future growth of space, aircraft, and defense industries in the USA. However, the processing-structure-property relationships in these materials remain poorly understood. In the present ASEE/NASA Summer Research Program, the plastic deformation modes and toughening mechanisms in single-phase and multiphase thermoset resins were investigated. Both thermoplastic and thermoset polyimide resins and their interpenetrating networks (IPNs and semi-IPNs) were included. The fundamental tendency to undergo strain localization (crazing and shear banding) as opposed to a more diffuse (or homogeneous) deformation in these polymers were evaluated. Other possible toughening mechanisms in multiphase thermoset resins were also examined. The topological features of network chain configuration/conformation and the multiplicity of phase morphology in INPs and semi-IPNs provide unprecedented opportunities for studying the toughening mechanisms in multiphase thermoset polymers and their fiber composites.

  13. Bismaleimide Copolymer Matrix Resins

    NASA Technical Reports Server (NTRS)

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

    1987-01-01

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

  14. Chemoviscosity modeling for thermosetting resin systems, 4

    NASA Technical Reports Server (NTRS)

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

    1989-01-01

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

  15. 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.

  16. Reactive Additives for Phenylethynyl-Containing Resins

    NASA Technical Reports Server (NTRS)

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

    2005-01-01

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

  17. 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

  18. The crystallization of tough thermoplastic resins in the presence of carbon fibers

    NASA Technical Reports Server (NTRS)

    Theil, M. H.

    1986-01-01

    The crystallization kinetics of the thermoplastic resins poly(phenylene sulfide) (PPS) and poly(aryl-ether-ether-ketone) (PEEK) in the presence and in the abscence of carbon fibers was studied. How carbon fiber surfaces in composites affect the crystallization of tough thermoplastic polymers that may serve as matrix resins were determined. The crystallization kinetics of such substances can provide useful information about the crystallization mechanisms and, thus, indicate if the presence of carbon fibers cause any changes in such mechanisms.

  19. Development of optically transparent cyclic olefin photoresist binder resins

    NASA Astrophysics Data System (ADS)

    Rhodes, Larry F.; Chang, Chun; Burns, Cheryl; Barnes, Dennis A.; Bennett, Brian; Seger, Larry; Wu, Xiaoming; Sobek, Andy; Mishak, Mike; Peterson, Craig; Langsdorf, Leah; Hada, Hideo; Shimizu, Hiroaki; Sasaki, Kazuhito

    2005-05-01

    Of all candidate 193 nm photoresist binder resins, transition metal catalyzed vinyl addition cyclic olefin (i.e., norbornene) polymers (PCO) hold the promise of high transparency and excellent etch resistance. In order to access lower molecular weight polymers, which are typically used in photoresists, α-olefin chain transfer agents (CTAs) are used in synthesizing vinyl addition poly(norbornenes). For example, HFANB (α,α-bis(trifluoromethyl)bicyclo [2.2.1]hept-5-ene-2-ethanol) homopolymers (p(HFANB)) with molecular weights (Mn) less than 5000 have been synthesized using such chain transfer agents. However, the optical density (OD) at 193 nm of these materials was found to rise as their molecular weights decreased consistent with a polymer end group effect. Extensive NMR and MS analysis of these polymers revealed that olefinic end groups derived from the chain transfer agent were responsible for the deleterious rise in OD. Chemical modification of these end groups by epoxidation, hydrogenation, hydrosilation, etc. lowers the OD of the polymer by removing the olefinic chromophore, however, it does require a second synthetic step. Thus a new class of non-olefinic chain transfer agents has been developed at Promerus that allow for excellent control of vinyl addition cyclic olefin polymer molecular weight and low optical density without the need of a post-polymerization chemical modification. Low molecular weight homopolymers of HFANB have been synthesized using these chain transfer agents that exhibit ODs <= 0.07 absorbance units per micron. This molecular weight control technology has been applied to both positive tone and negative tone vinyl addition cyclic olefin binder resins. Lithographic and etch performance of positive tone photoresists based on these binder resins will be presented.

  20. Moisture effects on the high-temperature strength of fiber-reinforced resin composites.

    NASA Technical Reports Server (NTRS)

    Hertz, J.

    1972-01-01

    Under NAS 8-27435, the Convair Aerospace Division of General Dynamics and their subcontractor, Hercules Incorporated, have conducted studies on the effects of moisture on the properties of fiber-reinforced resin composites and on the epoxy resins presently used in advanced composites. Data are presented on the resins and composites subjected to varying time/temperature/humidity or time/temperature/water-boil exposures. The effects of moisture on matrix, reinforcement, and fiber/resin interface are discussed and supported by experimental test data.

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

    DOEpatents

    Ebra, Martha A.; Wallace, Richard M.

    1983-01-01

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

  2. Low-level waste data base development - EPICOR II resin/liner investigation - a program review

    SciTech Connect

    McConnell, J.W. Jr.; Reno, H.W.; Schmitt, R.C.; Ayers, A.L. Jr.

    1986-01-01

    This paper presents an overview of the titled program and gives the status of the work on resin degradation, resin solidification, and field testing of solidified samples. A brief discussion of some recent results also is included. Resin materials from EPICOR-II prefilters used during cleanup of Three Mile Island Nuclear Power Station are being examined to (a) develop a data base for low-level waste and (b) obtain information on survivability of waste forms composed of ion exchange media loaded with radionuclides and solidified in matrices of cement and Dow polymer. An unusual aspect of the investigation is the use of commercial grade resins which have been loaded with over five times the radioactivity normally seen in a commercial application. That dramatically increases the total radiation dose to the resins. 21 refs., 8 figs.

  3. Low level waste data base development - EPICOR-II resin/liner investigation. Program review

    SciTech Connect

    McConnell, J.W. Jr.

    1985-09-10

    This paper presents an overview of the titled program and gives the status of the work on resin degradation, resin solidification, and field testing of solidified samples. A brief discussion of some recent results is also included. Resin materials from EPICOR-II prefilters used in the cleanup of the Three Mile Island Nuclear Power Station are being examined to (1) develop a low level waste data base and (2) obtain information on survivability of waste forms composed of ion exchange media loaded with radionuclides and solidified in matrices of cement and Dow polymer. An unusual aspect of this investigation is the use of commercial grade resins which have been loaded with over five times the radioactivity normally seen in a commercial application. That dramatically increases the total radiation dose to the resins. 18 refs., 8 figs.

  4. Isosorbide as the structural component of bio-based unsaturated polyesters for use as thermosetting resins.

    PubMed

    Sadler, Joshua M; Toulan, Faye R; Nguyen, Anh-Phuong T; Kayea, Ronald V; Ziaee, Saeed; Palmese, Giuseppe R; La Scala, John J

    2014-01-16

    In recent years, the development of renewable bio-based resins has gained interest as potential replacements for petroleum based resins. Modified carbohydrate-based derivatives have favorable structural features such as fused bicyclic rings that offer promising candidates for the development of novel renewable polymers with improved thermomechanical properties when compared to early bio-based resins. Isosorbide is one such compound and has been utilized as the stiffness component for the synthesis of novel unsaturated polyesters (UPE) resins. Resin blends of BioUPE systems with styrene were shown to possess viscosities (120-2200 cP) amenable to a variety of liquid molding techniques, and after cure had Tgs (53-107 °C) and storage moduli (430-1650 MPa) that are in the desired range for composite materials. These investigations show that BioUPEs containing isosorbide can be tailored during synthesis of the prepolymer to meet the needs of different property profiles. PMID:24188843

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

    DOEpatents

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

    1982-05-05

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

  6. Maleimide Functionalized Siloxane Resins

    SciTech Connect

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

    1999-04-21

    In-situ filling through hydrolysis and condensation of silicon alkoxides has been utilized to generate nanocomposites in which the filler phase can be intimately associated with the polymer on relatively small length scales. One problem of the method has been achieving useful fill volumes without bulk phase separation of the reacting silicon monomer from the polymer. In this paper, we describe the preparation of a new class of nanocomposite materials in which the inorganic filler phase is pre-assembled before copolymerization with an organic species. Maleimide monomers, prepared from alkoxysilylpropyl amines and maleic anhydride, were protected against side reactions by forming the oxonorbornene Diels-Alder adduct with furan. The monomers were then reacted under sol-gel conditions to form oligomers or polymers-the filler phase. The material was activated by thermal deprotection of the maleimide and reacted with organic monomers or polymers to form the filled nanocomposite.

  7. Quantitation of buried contamination by use of solvents. Part 1: Solvent degradation of amine cured epoxy resins

    NASA Technical Reports Server (NTRS)

    Rheineck, A. E.; Heskin, R. A.; Hill, L. W.

    1972-01-01

    The solubility and/or swelling of cured epoxy resins was studied using the solubility parameter method. Determination of solubility parameters were found in order to select solvents for solvent-assisted degradation of cured epoxy polymers used in spacecraft. A method for improving recovery of seeded spores is suggested for assay of buried contaminants. Three commercial epoxy resins were cured using four different alkyl amines. For each resin-amine combination, three levels of amine were used, corresponding to 1/3, 2/3, and all of the amine required to react with the oxirane groups of the resin. The solubility parameters of the 36 resulting model compounds were determined in poorly and moderately hydrogen-bonded solvents. No strongly hydrogen-bonded solvents caused dissolution or swelling. The tolerance of cured resins is discussed in terms of polymer structure.

  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. Status of high-temperature laminating resins and adhesives

    NASA Technical Reports Server (NTRS)

    Hergenrother, P. M.; Johnston, N. J.

    1980-01-01

    High-temperature polymers now being developed as adhesives and composite matrices are reviewed, including aromatic polyimides, polybenzimidazoles, polyphenylquinoxalines, nadic end-capped imide oligomers, maleimide end-capped oligomers, and acetylene-terminated imide oligomers. The mechanical properties of laminates based on these resins are reported together with preliminary test results on the adhesive properties for titanium-to-titanium and composite-to-composite lap shear specimens.

  10. Statistical Design in Isothermal Aging of Polyimide Resins

    NASA Technical Reports Server (NTRS)

    Sutter, James K.; Jobe, Marcus; Crane, Elizabeth A.

    1995-01-01

    Recent developments in research on polyimides for high temperature applications have led to the synthesis of many new polymers. Among the criteria that determines their thermal oxidative stability, isothermal aging is one of the most important. Isothermal aging studies require that many experimental factors are controlled to provide accurate results. In this article we describe a statistical plan that compares the isothermal stability of several polyimide resins, while minimizing the variations inherent in high-temperature aging studies.

  11. Next generation of PTFE resins for improved performance in CPI

    SciTech Connect

    Libert, S.A.; Ebnesajjad, S.

    1999-11-01

    Polytetrafluoroethylene (PTFE) polymers are well known for chemical resistance, low friction, dielectric constant, purity and broad temperature range. A second generation of granular PTFE resins has been specially designed to provide additional characteristics while maintaining all of the basic properties of PTFE. The new properties, which include resistance to permeation and creep, weldability, increased dielectric breakdown strength and smooth surface are reviewed in the following discussion.

  12. Polyimide molding powder, coating, adhesive, and matrix resin

    NASA Technical Reports Server (NTRS)

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

    1992-01-01

    The invention is a polyimide prepared from 3,4'-oxydianiline (3,4'-ODA) and 4,4'-oxydiphthalic anhydride (ODPA), in 2-methoxyethyl ether (diglyme). The polymer was prepared in ultra high molecular weight and in a controlled molecular weight form which has a 2.5 percent offset in stoichiometry (excess diamine) with a 5.0 percent level of phthalic anhydride as an endcap. This controlled molecular weight form allows for greatly improved processing of the polymer for moldings, adhesive bonding, and composite fabrication. The higher molecular weight version affords tougher films and coatings. The overall polymer structure groups in the dianhydride, the diamine, and a metal linkage in the diamine affords adequate flow properties for making this polymer useful as a molding powder, adhesive, and matrix resin.

  13. Ballistic impact behavior of carbon nanotube and nanosilica dispersed resin and composites

    NASA Astrophysics Data System (ADS)

    Pandya, K. S.; Akella, K.; Joshi, M.; Naik, N. K.

    2012-12-01

    Experimental studies are presented on the ballistic impact behavior of nanoparticle dispersed materials viz. symmetric balanced cross-ply laminates made using unidirectional E-glass fabric with epoxy resin and neat epoxy resin. The nanoparticles used are nanosilica and multi-walled carbon nanotube for polymer matrix composites and nanosilica for epoxy resin. For comparison, studies are carried out on symmetric balanced cross-ply E-glass/epoxy and neat epoxy resin without nanoparticles. Effect of nanoparticle dispersion on ballistic limit velocity, V50 and energy absorbed has been studied. It is observed that V50 can be enhanced up to 6.3% for polymer matrix composites and up to 7.3% for neat resin on addition of nanoparticles. Also, energy absorbed can be increased up to 13.0% for polymer matrix composites and up to 15.2% for neat resin on addition of nanoparticles. Damage and energy absorbing mechanisms for different types of materials studied is also presented. Further, it is observed that the damage size on the target around the point of impact decreases on addition of nanoparticles. Quantitative data are given for high velocity impact behavior of the five types of specimens studied.

  14. 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.

  15. A new polyimide laminatine resin

    NASA Technical Reports Server (NTRS)

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

    1977-01-01

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

  16. A semi-empirical approach for the chemoviscosity modeling of reactive resin system

    NASA Technical Reports Server (NTRS)

    Hou, T. H.; Bai, J. M.

    1988-01-01

    A new analytical model for simulating chemoviscosity of a thermosetting resin is presented. The model is developed on the basis of the Williams-Landel-Ferry (WLF, 1955) polymer rheology theory for the thermoplastic materials, which was modified to account for the factor of reaction time by introducing a relationship between the glass transition temperature and the degree of cure of the resin system. Theoretical predictions of the chemoviscosity profiles under dynamic curing conditions are shown to compare favorably with the experimental data obtained on the Hercules 3501-6 resin system cured under seven isothermal conditions.

  17. RESORCINOL-FORMALDEHYDE ION EXCHANGE RESIN CHEMISTRY FOR HIGH LEVEL WASTE TREATMENT

    SciTech Connect

    Nash, C.; Duignan, M.

    2010-01-14

    A principal goal at the Savannah River Site is to safely dispose of the large volume of liquid nuclear waste held in many storage tanks. In-tank ion exchange technology is being considered for cesium removal using a polymer resin made of resorcinol formaldehyde that has been engineered into microspheres. The waste under study is generally lower in potassium and organic components than Hanford waste; therefore, the resin performance was evaluated with actual dissolved salt waste. The ion exchange performance and resin chemistry results are discussed.

  18. An in situ study of resin-assisted solvothermal metal-organic framework synthesis

    NASA Astrophysics Data System (ADS)

    Moorhouse, Saul J.; Wu, Yue; O'Hare, Dermot

    2016-04-01

    A newly developed in situ monochromatic high-energy X-ray diffraction setup was used to investigate the synthesis of MOFs using cation-impregnated polymer resin beads as a ion source. The Co-NDC-DMF (NDC=2,6-naphthalenedicarboxylate; DMF=dimethylformamide) system was investigated, a system which is known to produce at least three distinct frameworks. It was found that the resin-assisted synthesis results in the preferential formation of a topology previously impossible to synthesise in bulk, while the comparable nitrate-salt synthesis appeared to form an alternative phases. It was also found that the resin-assisted synthesis is highly diffusion-controlled.

  19. Polymerization-Induced Phase Separation in Vinyl Ester Resins

    NASA Astrophysics Data System (ADS)

    Ganglani, Manisha; Torkelson, John; Carr, Stephen

    2000-03-01

    In certain multi-component, crosslinking polymer systems, phase separation is induced by polymerization, a process call polymerization-induced phase separation (PIPS) in which there exists a competition between reaction rate and phase separation rate. The final morphology and properties of a system that experiences PIPS depend on the outcome of this competition. Thus, by controlling these rates, it would be possible to control end properties. In fact, this theory has been applied for the creation of polymer-dispersed liquid crystals (PDLCs) where cure occurs via condensation reactions or via free radical polymerization initiated by UV light. This research examines PIPS in the vinyl ester (VE) resins, which are popular as matrix materials in polymer composites. Cure of the VE resins is more complicated because it uses initiators and therefore requires more time and offers less control than cure by photopolymerization. To better understand the PIPS process in the VE resins, this research separates the two competitive effects and examines each one in turn. Initial experiments use a model system to focus on the effect of PIPS in the absence of crosslinking.

  20. Polymers for Drug Delivery Systems

    PubMed Central

    Liechty, William B.; Kryscio, David R.; Slaughter, Brandon V.; Peppas, Nicholas A.

    2012-01-01

    Polymers have played an integral role in the advancement of drug delivery technology by providing controlled release of therapeutic agents in constant doses over long periods, cyclic dosage, and tunable release of both hydrophilic and hydrophobic drugs. From early beginnings using off-the-shelf materials, the field has grown tremendously, driven in part by the innovations of chemical engineers. Modern advances in drug delivery are now predicated upon the rational design of polymers tailored for specific cargo and engineered to exert distinct biological functions. In this review, we highlight the fundamental drug delivery systems and their mathematical foundations and discuss the physiological barriers to drug delivery. We review the origins and applications of stimuli-responsive polymer systems and polymer therapeutics such as polymer-protein and polymer-drug conjugates. The latest developments in polymers capable of molecular recognition or directing intracellular delivery are surveyed to illustrate areas of research advancing the frontiers of drug delivery. PMID:22432577

  1. High-Performance, Semi-Interpenetrating Polymer Network

    NASA Technical Reports Server (NTRS)

    Pater, Ruth H.; Lowther, Sharon E.; Smith, Janice Y.; Cannon, Michelle S.; Whitehead, Fred M.; Ely, Robert M.

    1992-01-01

    High-performance polymer made by new synthesis in which one or more easy-to-process, but brittle, thermosetting polyimides combined with one or more tough, but difficult-to-process, linear thermoplastics to yield semi-interpenetrating polymer network (semi-IPN) having combination of easy processability and high tolerance to damage. Two commercially available resins combined to form tough, semi-IPN called "LaRC-RP49." Displays improvements in toughness and resistance to microcracking. LaRC-RP49 has potential as high-temperature matrix resin, adhesive, and molding resin. Useful in aerospace, automotive, and electronic industries.

  2. Bio-inspired Construction of Advanced Fuel Cell Cathode with Pt Anchored in Ordered Hybrid Polymer Matrix.

    PubMed

    Xia, Zhangxun; Wang, Suli; Jiang, Luhua; Sun, Hai; Liu, Shuang; Fu, Xudong; Zhang, Bingsen; Sheng Su, Dang; Wang, Jianqiang; Sun, Gongquan

    2015-01-01

    The significant use of platinum for catalyzing the cathodic oxygen reduction reactions (ORRs) has hampered the widespread use of polymer electrolyte membrane fuel cells (PEMFCs). The construction of well-defined electrode architecture in nanoscale with enhanced utilization and catalytic performance of Pt might be a promising approach to address such barrier. Inspired by the highly efficient catalytic processes in enzymes with active centers embedded in charge transport pathways, here we demonstrate for the first time a design that allocates platinum nanoparticles (Pt NPs) at the boundaries with dual-functions of conducting both electrons by aid of polypyrrole and protons via Nafion(®) ionomer within hierarchical nanoarrays. By mimicking enzymes functionally, an impressive ORR activity and stability is achieved. Using this brand new electrode architecture as the cathode and the anode of a PEMFC, a high mass specific power density of 5.23 W mg(-1)Pt is achieved, with remarkable durability. These improvements are ascribed to not only the electron decoration and the anchoring effects from the Nafion(®) ionomer decorated PPy substrate to the supported Pt NPs, but also the fast charge and mass transport facilitated by the electron and proton pathways within the electrode architecture. PMID:26537781

  3. Advanced control of liquid water region in diffusion media of polymer electrolyte fuel cells through a dimensionless number

    NASA Astrophysics Data System (ADS)

    Wang, Yun; Chen, Ken S.

    2016-05-01

    In the present work, a three-dimension (3-D) model of polymer electrolyte fuel cells (PEFCs) is employed to investigate the complex, non-isothermal, two-phase flow in the gas diffusion layer (GDL). Phase change in gas flow channels is explained, and a simplified approach accounting for phase change is incorporated into the fuel cell model. It is found that the liquid water contours in the GDL are similar along flow channels when the channels are subject to two-phase flow. Analysis is performed on a dimensionless parameter Da0 introduced in our previous paper [Y. Wang and K. S. Chen, Chemical Engineering Science 66 (2011) 3557-3567] and the parameter is further evaluated in a realistic fuel cell. We found that the GDL's liquid water (or liquid-free) region is determined by the Da0 number which lumps several parameters, including the thermal conductivity and operating temperature. By adjusting these factors, a liquid-free GDL zone can be created even though the channel stream is two-phase flow. Such a liquid-free zone is adjacent to the two-phase region, benefiting local water management, namely avoiding both severe flooding and dryness.

  4. Recent advances in thromboresistant and antimicrobial polymers for biomedical applications: just say yes to nitric oxide (NO).

    PubMed

    Wo, Yaqi; Brisbois, Elizabeth J; Bartlett, Robert H; Meyerhoff, Mark E

    2016-08-19

    Biomedical devices are essential for patient diagnosis and treatment; however, when blood comes in contact with foreign surfaces or homeostasis is disrupted, complications including thrombus formation and bacterial infections can interrupt device functionality, causing false readings and/or shorten device lifetime. Here, we review some of the current approaches for developing antithrombotic and antibacterial materials for biomedical applications. Special emphasis is given to materials that release or generate low levels of nitric oxide (NO). Nitric oxide is an endogenous gas molecule that can inhibit platelet activation as well as bacterial proliferation and adhesion. Various NO delivery vehicles have been developed to improve NO's therapeutic potential. In this review, we provide a summary of the NO releasing and NO generating polymeric materials developed to date, with a focus on the chemistry of different NO donors, the polymer preparation processes, and in vitro and in vivo applications of the two most promising types of NO donors studied thus far, N-diazeniumdiolates (NONOates) and S-nitrosothiols (RSNOs). PMID:27226170

  5. Bio-inspired Construction of Advanced Fuel Cell Cathode with Pt Anchored in Ordered Hybrid Polymer Matrix

    NASA Astrophysics Data System (ADS)

    Xia, Zhangxun; Wang, Suli; Jiang, Luhua; Sun, Hai; Liu, Shuang; Fu, Xudong; Zhang, Bingsen; Sheng Su, Dang; Wang, Jianqiang; Sun, Gongquan

    2015-11-01

    The significant use of platinum for catalyzing the cathodic oxygen reduction reactions (ORRs) has hampered the widespread use of polymer electrolyte membrane fuel cells (PEMFCs). The construction of well-defined electrode architecture in nanoscale with enhanced utilization and catalytic performance of Pt might be a promising approach to address such barrier. Inspired by the highly efficient catalytic processes in enzymes with active centers embedded in charge transport pathways, here we demonstrate for the first time a design that allocates platinum nanoparticles (Pt NPs) at the boundaries with dual-functions of conducting both electrons by aid of polypyrrole and protons via Nafion® ionomer within hierarchical nanoarrays. By mimicking enzymes functionally, an impressive ORR activity and stability is achieved. Using this brand new electrode architecture as the cathode and the anode of a PEMFC, a high mass specific power density of 5.23 W mg-1Pt is achieved, with remarkable durability. These improvements are ascribed to not only the electron decoration and the anchoring effects from the Nafion® ionomer decorated PPy substrate to the supported Pt NPs, but also the fast charge and mass transport facilitated by the electron and proton pathways within the electrode architecture.

  6. Bio-inspired Construction of Advanced Fuel Cell Cathode with Pt Anchored in Ordered Hybrid Polymer Matrix

    PubMed Central

    Xia, Zhangxun; Wang, Suli; Jiang, Luhua; Sun, Hai; Liu, Shuang; Fu, Xudong; Zhang, Bingsen; Sheng Su, Dang; Wang, Jianqiang; Sun, Gongquan

    2015-01-01

    The significant use of platinum for catalyzing the cathodic oxygen reduction reactions (ORRs) has hampered the widespread use of polymer electrolyte membrane fuel cells (PEMFCs). The construction of well-defined electrode architecture in nanoscale with enhanced utilization and catalytic performance of Pt might be a promising approach to address such barrier. Inspired by the highly efficient catalytic processes in enzymes with active centers embedded in charge transport pathways, here we demonstrate for the first time a design that allocates platinum nanoparticles (Pt NPs) at the boundaries with dual-functions of conducting both electrons by aid of polypyrrole and protons via Nafion® ionomer within hierarchical nanoarrays. By mimicking enzymes functionally, an impressive ORR activity and stability is achieved. Using this brand new electrode architecture as the cathode and the anode of a PEMFC, a high mass specific power density of 5.23 W mg−1Pt is achieved, with remarkable durability. These improvements are ascribed to not only the electron decoration and the anchoring effects from the Nafion® ionomer decorated PPy substrate to the supported Pt NPs, but also the fast charge and mass transport facilitated by the electron and proton pathways within the electrode architecture. PMID:26537781

  7. Protection of Conductive and Non-conductive Advanced Polymer-based Paints from Highly Aggressive Oxidative Environments

    NASA Technical Reports Server (NTRS)

    Gudimenko, Y.; Ng, R.; Iskanderova, Z.; Kleiman, J.; Grigorevsky, A.; Kiseleva, L.; Finckenor, M.; Edwards, D.

    2005-01-01

    Research has been continued to further improve the space durability of conductive and non-conductive polymer-based paints and of conductive thermal control paints for space applications. Efforts have been made to enhance the space durability and stability of functional Characteristics in ground-based space environment imitating conditions, using specially developed surface modification treatment. The results of surface modification of new conductive paints, including the ground-based testing in aggressive oxidative environments, such as atomic oxygen/UV and oxygen plasma, and performance evaluation are presented. Functional properties and performance characteristics, such as thermal optical properties (differential solar absorptance and thermal emittance representing the thermal optical performance of thermal control paints) and surface resistivity characteristics of pristine, surface modified, and tested materials were verified. Extensive surface analysis studies have been performed using complementary surface analyses including SEM/EDS and XPS. Test results revealed that the successfully treated materials exhibit reduced mass loss and no surface morphology change, thus indicating good protection from the severe oxidative environment. It was demonstrated that the developed surface modification treatment could be applied successfully to charge dissipative and conductive paints.

  8. Polymer films

    DOEpatents

    Granick, Steve; Sukhishvili, Svetlana A.

    2004-05-25

    A film contains a first polymer having a plurality of hydrogen bond donating moieties, and a second polymer having a plurality of hydrogen bond accepting moieties. The second polymer is hydrogen bonded to the first polymer.

  9. Polymer films

    DOEpatents

    Granick, Steve; Sukhishvili, Svetlana A.

    2008-12-30

    A film contains a first polymer having a plurality of hydrogen bond donating moieties, and a second polymer having a plurality of hydrogen bond accepting moieties. The second polymer is hydrogen bonded to the first polymer.

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

    Code of Federal Regulations, 2014 CFR

    2014-07-01

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

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

    Code of Federal Regulations, 2011 CFR

    2011-07-01

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

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

    Code of Federal Regulations, 2010 CFR

    2010-07-01

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

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

    Code of Federal Regulations, 2013 CFR

    2013-07-01

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

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

    Code of Federal Regulations, 2012 CFR

    2012-07-01

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

  15. Advanced textile applications for primary aircraft structures

    NASA Technical Reports Server (NTRS)

    Jackson, Anthony C.; Barrie, Ronald E.; Shah, Bharat M.; Shukla, Jay G.

    1992-01-01

    Advanced composite primary structural concepts were evaluated for low cost, damage tolerant structures. Development of advanced textile preforms for fuselage structural applications with resin transfer molding and powder epoxy materials are now under development.

  16. Advanced textile applications for primary aircraft structures

    NASA Technical Reports Server (NTRS)

    Jackson, Anthony C.; Barrie, Ronald E.; Shah, Bharat M.; Shukla, Jay G.

    1992-01-01

    Advanced composite primary structural concepts have been evaluated for low cost, damage tolerant structures. Development of advanced textile preforms for fuselage structural applications with resin transfer molding and powder epoxy material is now under development.

  17. Magnetic and magnetoresistance behaviors of particulate iron/vinyl ester resin nanocomposites

    NASA Astrophysics Data System (ADS)

    Guo, Zhanhu; Hahn, H. Thomas; Lin, Hongfei; Karki, Amar B.; Young, David P.

    2008-07-01

    Magnetoresistance (MR) behavior of vinyl ester monomer stabilized iron nanoparticles and heat-treated vinyl ester resin nanocomposites reinforced with iron nanoparticles were investigated. Vinyl ester monomer serves as a coupling agent with one side covalently bound onto the nanoparticle surface by a displacement reaction and the other end copolymerized with extra vinyl ester resin to form a robust entity. The particle loading and type of material (polymer or carbonized polymer) have a significant effect on the magnetic and MR properties. The heat-treated nanocomposites follow a tunneling conduction. After reduction annealing, the obtained nanocomposites possess a room temperature MR of 8.3 % at a field of 90 kOe.

  18. Synthesis and characterization of a novel polymer-ceramic system for biodegradable composite applications.

    PubMed

    Yang, Liu; Wang, Jian; Hong, Jason; Santerre, J Paul; Pilliar, Robert M

    2003-09-01

    The objective of this study was to develop a biodegradable polymer resin that could be used for the fabrication of an interpenetrating phase composite (IPC) made of porous calcium polyphosphate (CPP) and an organic polymer resin. The resin was synthesized from a polycarbonate-based divinyl oligomer and monomers containing ionic groups. The physical and chemical properties of the polymer resin and polycarbonate-based divinyl oligomer were characterized by gel permeation chromatography, Fourier transform infrared spectroscopy, and swelling studies. The in vitro degradation of the polymer resins was assessed using cholesterol esterase in a buffer solution at 37 degrees C for 3 weeks. Scanning electron microscopy of the degraded samples indicated that the hydrolysis of the resin was catalyzed by the enzyme. The relative interfacial shear strength between the polymer resin and the CPP ceramic was studied using a microbond test. The addition of ionic groups into the polymer resin chains appeared to improve the chemical bonding between the polymer and the CPP. Preliminary mechanical properties of the IPC were investigated by determining bending strength using a three point bending test. The data showed a sevenfold increase in strength over that of the monolithic CPP, and the addition of more ionic groups into the resin led to a higher bending strength for the newly formed CPP/polycarbonate resin system. Sample cross sections of the IPC examined using scanning electron microscopy suggested that the resin had infiltrated almost all of the pores of the CPP. The results of this study indicate that the IPC could potentially be used for fabricating novel biodegradable load-bearing implants. PMID:12918046

  19. 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.

  20. Synthesis of a Self-Healing Polymer Based on Reversible Diels-Alder Reaction: An Advanced Undergraduate Laboratory at the Interface of Organic Chemistry and Materials Science

    ERIC Educational Resources Information Center

    Weizman, Haim; Nielsen, Christian; Weizman, Or S.; Nemat-Nasser, Sia

    2011-01-01

    This laboratory experiment exposes students to the chemistry of self-healing polymers based on a Diels-Alder reaction. Students accomplish a multistep synthesis of a monomer building block and then polymerize it to form a cross-linked polymer. The healing capability of the polymer is verified by differential scanning calorimetry (DSC) experiments.…

  1. Preparation of codeine-resinate and chlorpheniramine-resinate sustained-release suspension and its pharmacokinetic evaluation in beagle dogs.

    PubMed

    Zeng, Huan-Xiang; Cheng, Gang; Pan, Wei-San; Zhong, Guo-Ping; Huang, Min

    2007-06-01

    Using ion exchange resins (IERs) as carriers, a dual-drug sustained release suspension containing codeine, and chlorpheniramine had been prepared to elevate drug safety, effectiveness and conformance. The codeine resinate and chlorpheniramine resinate beads were prepared by a batch process and then impregnated with Polyethylene glycol 4000 (PEG 4000), respectively. The PEG impregnated drug resinate beads were coated with ethylcellulose as the coating polymer and di-n-butyl-phthalate as plasticizer in ethanol and methylene chloride mixture by the Wurster process. The coated PEG impregnated drug resinate beads were dispersed in an aqueous suspending vehicle containing 0.5% w/w xanthan gum and 0.5% w/w of hydroxypropylmethylcellulose of nominal viscosity of 4000 cps, obtaining codeine resinate and chlorpheniramine resinate sustained-release suspension (CCSS). Codeine phosphate and chlorpheniramine maleate were respectively loaded onto AMBERLITE IRP 69, and PEG 4000 was used to impregnate drug resinate beads to maintain their geometry. Ethylcellulose with di-n-butyl-phthalate in ethanol and methylene chloride mixture for the coating of drug resinate beads was performed in Glatt fluidized bed coater, where the coating solution flow rate was 8-12 g/min, the inlet air temperature was 50-60 degrees C, the outlet air temperature was 32-38 degrees C, the atomizing air pressure was 2.0 bar and the fluidized air pressure was adjusted as required. Few significant agglomeration of circulating drug resinate beads was observed during the operation. The film weight gained 20% w/w and 15% w/w were suitable for the PEG impregnated codeine resinate and chlorpheniramine resinate beads, respectively. Residual solvent content increased with coating level, but inprocess drying could reduce residual solvent content. In the present study, the rates of drug release from both drug resinate beads were measured in 0.05 M and 0.5M KCl solutions. The increased ionic strength generally accelerated

  2. Semi-interpenetrating polymer network for tougher and more microcracking resistant high temperature polymers

    NASA Technical Reports Server (NTRS)

    Pater, Ruth H. (Inventor)

    1992-01-01

    This invention is a semi-interpenetrating polymer network which includes a high performance thermosetting polyimide having a nadic end group acting as a crosslinking site and a high performance linear thermoplastic polyimide. An improved high temperature matrix resin is provided which is capable of performing at 316 C in air for several hundreds of hours. This resin has significantly improved toughness and microcracking resistance, excellent processability and mechanical performance, and cost effectiveness.

  3. Advanced microwave processing concepts

    SciTech Connect

    Lauf, R.J.; McMillan, A.D.; Paulauskas, F.L.

    1995-05-01

    The purpose of this work is to explore the feasibility of several advanced microwave processing concepts to develop new energy-efficient materials and processes. The project includes two tasks: (1) commercialization of the variable-frequency microwave furnace; and (2) microwave curing of polymer composites. The variable frequency microwave furnace, whose initial conception and design was funded by the AIC Materials Program, will allow us, for the first time, to conduct microwave processing studies over a wide frequency range. This novel design uses a high-power traveling wave tube (TWT) originally developed for electronic warfare. By using this microwave source, one can not only select individual microwave frequencies for particular experiments, but also achieve uniform power densities over a large area by the superposition of many different frequencies. Microwave curing of thermoset resins will be studied because it hold the potential of in-situ curing of continuous-fiber composites for strong, lightweight components. Microwave heating can shorten curing times, provided issues of scaleup, uniformity, and thermal management can be adequately addressed.

  4. 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

  5. High elastic modulus nanopowder reinforced resin composites for dental applications

    NASA Astrophysics Data System (ADS)

    Wang, Yijun

    2007-12-01

    effective coupling agents and higher filler loading, viscous flow can be greatly decreased due to the attenuation of mobility of polymer chains. Complementary studies indicate that our resin composites are promising for the proposed applications as a stiff support to all-ceramic crowns.

  6. Objective Surface Evaluation of Fiber Reinforced Polymer Composites

    NASA Astrophysics Data System (ADS)

    Palmer, Stuart; Hall, Wayne

    2013-08-01

    The mechanical properties of advanced composites are essential for their structural performance, but the surface finish on exterior composite panels is of critical importance for customer satisfaction. This paper describes the application of wavelet texture analysis (WTA) to the task of automatically classifying the surface finish properties of two fiber reinforced polymer (FRP) composite construction types (clear resin and gel-coat) into three quality grades. Samples were imaged and wavelet multi-scale decomposition was used to create a visual texture representation of the sample, capturing image features at different scales and orientations. Principal components analysis was used to reduce the dimensionality of the texture feature vector, permitting successful classification of the samples using only the first principal component. This work extends and further validates the feasibility of this approach as the basis for automated non-contact classification of composite surface finish using image analysis.

  7. Understanding the nano- and macromechanical behaviour, the failure and fatigue mechanisms of advanced and natural polymer fibres by Raman/IR microspectrometry

    NASA Astrophysics Data System (ADS)

    Colomban, Philippe

    2013-03-01

    The coupled mechanical and Raman/infrared (IR) analysis of the (nano)structure and texture of synthetic and natural polymer fibres (polyamides (PA66), polyethylene terephthalate (PET), polypropylene (PP), poly(paraphenylene benzobisoxazole) (PBO), keratin/hair, Bombyx mori, Gonometa rufobrunea/postica Antheraea/Tussah silkworms and Nephila Madagascarensis spider silks) is applied so as to differentiate between crystalline and amorphous macromolecules. Bonding is very similar in the two cases but a broader distribution of conformations is observed for the amorphous macromolecules. These conclusions are then used to discuss the modifications induced by the application of a tensile or compressive stress, including the effects of fatigue. Detailed attention is paid to water and the inter-chain coupling for which the importance of hydrogen bonding is reconsidered. The significant role of the ‘amorphous’ bonds/domains in the process of fracture/fatigue is shown. Invited talk at the 6th International Workshop on Advanced Materials Science and Nanotechnology IWAMSN2012, 30 October-2 November 2012, Ha Long, Vietnam.

  8. Applications of advanced electrochemical techniques in the study of microbial fuel cells and corrosion protection by polymer coatings

    NASA Astrophysics Data System (ADS)

    Manohar, Aswin Karthik

    determined by the sum of the polarization resistance of the anode (Rap) and the cathode (Rcp), and therefore Rint depends on V. The ohmic contribution to the Rint was very small. It has been found that Rint decreased with decreasing cell voltage as the increasing current flow decreased R ap and Rcp. In the presence of MR-1, Rint was lower by a factor of about 100 than Rint of the MFC with buffer and lactate as anolyte. Additions of SS balls to the anode compartment produced a very large decrease of Rint. For the MFC containing SS balls in the anode compartment no significant further decrease of Rint could be observed when MR-1 was added to the anolyte. In Chapter 2, EIS has been used to determine the properties and stability of polymer coatings based on different chromate or chromate-free pretreatments and primers. Five sets of coated aluminum 2024 samples were exposed to 0.5N NaCl for a period of 31 days. Impedance spectra of the samples were measured during this period and the changes of the properties of the different coatings were studied as a function of time. From the analysis of the fit parameters of the impedance spectra, it was found that the corrosion protection of the coated samples depended on the type of primer used. The coating with the chromate based primer provided better corrosion protection than the coating with the chromate free primer. After 31 days of exposure, one sample from each set was scribed and exposed to 0.5N NaCl. The corrosion behavior of the scribed coatings was found to be dependent upon the type of pretreatment employed. The samples with the chromate conversion coating pretreatment showed better corrosion resistance in the scribed area than the samples that were treated by the trivalent chromium based method.

  9. 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.

  10. Indirect resin composites

    PubMed Central

    Nandini, Suresh

    2010-01-01

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

  11. Methods of Making and Using Shape Memory Polymer Composite Patches

    NASA Technical Reports Server (NTRS)

    Hood, Patrick J.

    2011-01-01

    A method of repairing a composite component having a damaged area including: laying a composite patch over the damaged area: activating the shape memory polymer resin to easily and quickly mold said patch to said damaged area; deactivating said shape memory polymer so that said composite patch retains the molded shape; and bonding said composite patch to said damaged part.

  12. Rheology, structure, and properties of new phosphate glass/polymer hybrids

    NASA Astrophysics Data System (ADS)

    Urman, Kevin Leonard

    Physical modification of structure and properties via polymer blending and reinforcement is a common practice in the plastics industry and has a large economic advantage over synthesizing new polymeric materials to fulfill new material needs. Despite the large amount of interest in polymer blends and composites, the currently available commercial materials cannot satisfy the growing need for new advanced materials. This need is being addressed in part by inorganic/organic hybrid materials. By blending low-TG phosphate glasses with polymeric materials, a new class of inorganic/organic hybrids can be created. These hybrids can be processed conventionally with glass loadings of up to 60% by volume or 90% by weight, making it possible to obtain significant improvements in properties that are impossible to achieve from classical polymer blends and composites. This class of inorganic/organic hybrids containing both the inorganic low-TG phosphate glass (Pglass) and the organic polymer are very unique materials because both hybrid components are fluid during processing. Thereby, providing the ability to tailor both the hybrid morphology and properties in unprecedented ways through carefully controlled processing. This dissertation discusses the continuing research into low-Tg tin fluorophosphate glass blended with commodity resins. The specific resins of interest are low density polyethylene (LDPE), polyamide 12, and polyamide 6. The shear rheology and the extensional flow characteristics of LDPE hybrids were studied to understand hybrid behavior under flow characteristics typical of many polymer processing techniques. The elongational flow was also utilized to generate unique morphologies, enhance crystallinity, and to alter polymer chain orientation. The extension of this field into interacting commodity resins like polyamide 12 and polyamide 6 yielded new hybrids with unprecedented properties. Polyamide 12 hybrids were used to build the first processing

  13. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

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

  14. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

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

  15. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

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

  16. 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...

  17. 21 CFR 178.3930 - Terpene resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

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

  18. 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

  19. 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.

  20. Grafted methylenediphosphonate ion exchange resins

    DOEpatents

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

    1997-04-08

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

  1. Grafted methylenediphosphonate ion exchange resins

    DOEpatents

    Trochimcznk, Andrzej W.; 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. Electrically conductive polymer concrete coatings

    DOEpatents

    Fontana, J.J.; Elling, D.; Reams, W.

    1988-05-26

    A sprayable electrically conductive polymer concrete coating for vertical and overhead applications is described. The coating is permeable yet has low electrical resistivity (<10 ohm-cm), good bond strength to concrete substrates, and good weatherability. A preferred formulation contains about 60 wt% calcined coke breeze, 40 wt% vinyl ester resin with 3.5 wt% modified bentonite clay. Such formulations apply evenly and provide enough rigidity for vertical or overhead structures so there is no drip or sag. 4 tabs.

  4. Simulated space environmental effects on some experimental high performance polymers

    NASA Technical Reports Server (NTRS)

    Connell, John W.

    1993-01-01

    High performance polymers for potential space applications were evaluated under simulated space environmental conditions. Experimental resins from blends of acetylene terminated materials, poly(arylene ether)s and low color polyimides were exposed to high energy electron and ultraviolet radiation in an attempt to simulate space environmental effects. Thin films, neat resin moldings, and carbon fiber reinforced composites were exposed, and the effect on certain polymer properties were determined. Recent research involving the effects of various radiation exposures on the physical, optical, and mechanical properties of several experimental polymer systems is reviewed.

  5. Resin-composite blocks for dental CAD/CAM applications.

    PubMed

    Ruse, N D; Sadoun, M J

    2014-12-01

    Advances in digital impression technology and manufacturing processes have led to a dramatic paradigm shift in dentistry and to the widespread use of computer-aided design/computer-aided manufacturing (CAD/CAM) in the fabrication of indirect dental restorations. Research and development in materials suitable for CAD/CAM applications are currently the most active field in dental materials. Two classes of materials are used in the production of CAD/CAM restorations: glass-ceramics/ceramics and resin composites. While glass-ceramics/ceramics have overall superior mechanical and esthetic properties, resin-composite materials may offer significant advantages related to their machinability and intra-oral reparability. This review summarizes recent developments in resin-composite materials for CAD/CAM applications, focusing on both commercial and experimental materials. PMID:25344335

  6. Shrinkage Stresses Generated during Resin-Composite Applications: A Review

    PubMed Central

    Schneider, Luis Felipe J.; Cavalcante, Larissa Maria; Silikas, Nick

    2010-01-01

    Many developments have been made in the field of resin composites for dental applications. However, the manifestation of shrinkage due to the polymerization process continues to be a major problem. The material's shrinkage, associated with dynamic development of elastic modulus, creates stresses within the material and its interface with the tooth structure. As a consequence, marginal failure and subsequent secondary caries, marginal staining, restoration displacement, tooth fracture, and/or post-operative sensitivity are clinical drawbacks of resin-composite applications. The aim of the current paper is to present an overview about the shrinkage stresses created during resin-composite applications, consequences, and advances. The paper is based on results of many researches that are available in the literature. PMID:20948573

  7. Resin-composite Blocks for Dental CAD/CAM Applications

    PubMed Central

    Ruse, N.D.; Sadoun, M.J.

    2014-01-01

    Advances in digital impression technology and manufacturing processes have led to a dramatic paradigm shift in dentistry and to the widespread use of computer-aided design/computer-aided manufacturing (CAD/CAM) in the fabrication of indirect dental restorations. Research and development in materials suitable for CAD/CAM applications are currently the most active field in dental materials. Two classes of materials are used in the production of CAD/CAM restorations: glass-ceramics/ceramics and resin composites. While glass-ceramics/ceramics have overall superior mechanical and esthetic properties, resin-composite materials may offer significant advantages related to their machinability and intra-oral reparability. This review summarizes recent developments in resin-composite materials for CAD/CAM applications, focusing on both commercial and experimental materials. PMID:25344335

  8. "Green" High-Temperature Polymers

    NASA Technical Reports Server (NTRS)

    Meador, Michael A.

    1998-01-01

    PMR-15 is a processable, high-temperature polymer developed at the NASA Lewis Research Center in the 1970's principally for aeropropulsion applications. Use of fiber-reinforced polymer matrix composites in these applications can lead to substantial weight savings, thereby leading to improved fuel economy, increased passenger and payload capacity, and better maneuverability. PMR-15 is used fairly extensively in military and commercial aircraft engines components seeing service temperatures as high as 500 F (260 C), such as the outer bypass duct for the F-404 engine. The current world-wide market for PMR-15 materials (resins, adhesives, and composites) is on the order of $6 to 10 million annually.

  9. Synthesis, structural characterization, and performance evaluation of resorcinol-formaldehyde (R-F) ion-exchange resin

    SciTech Connect

    Hubler, T.L.; Franz, J.A.; Shaw, W.J.; Bryan, S.A.; Hallen, R.T.; Brown, G.N.; Bray, L.A.; Linehan, J.C.

    1995-08-01

    The 177 underground storage tanks at the DOE`s Hanford Site contain an estimated 180 million tons of high-level radioactive wastes. It is desirable to remove and concentrate the highly radioactive fraction of the tank wastes for vitrification. Resorcinol-formaldehyde (R-F) resin, an organic ion-exchange resin with high selectivity and capacity for the cesium ion, which is a candidate ion-exchange material for use in remediation of tank wastes. The report includes information on the structure/function analysis of R-F resin and the synthetic factors that affect performance of the resin. CS-100, a commercially available phenol-formaldehyde (P-F) resin, and currently the baseline ion-exchanger for removal of cesium ion at Hanford, is compared with the R-F resin. The primary structural unit of the R-F resin was determined to consist of a 1,2,3,4-tetrasubstituted resorcinol ring unit while CS-100, was composed mainly of a 1,2,4-trisubstituted ring. CS-100 shows the presence of phenoxy-ether groups, and this may account for the much lower decontamination factor of CS-100 for cesium ion. Curing temperatures for the R-F resin were found to be optimal at 105--130C. At lower temperatures, insufficient curing, hence crosslinking, of the polymer resin occurs and selectivity for cesium drops. Curing at elevated temperatures leads to chemical degradation. Optimal particle size for R-F resin is in the range of 20--50 mesh-sized particles. R-F resin undergoes chemical degradation or oxidation which destroys ion-exchange sites. The ion-exchange sites (hydroxyl groups) are converted to quinones and ketones. CS-100, though it has much lower performance for cesium ion-exchange, is significantly more chemically stable than R-F resin. To gamma radiation, CS-100 is more radiolytically stable than R-F resin.

  10. Advances in electronic packaging technologies by ultra-small microvias, super-fine interconnections and low loss polymer dielectrics

    NASA Astrophysics Data System (ADS)

    Sundaram, Venkatesh

    The fundamental motivation for this dissertation is to address the widening interconnect gap between integrated circuit (IC) demands and package substrates specifically for high frequency digital-RF systems applications. Moore's law for CMOS ICs predicts that transistor density on ICs will double approximately every 18 months. Packaging of ICs at the 32nm and 22nm nodes in the next few years will require 20mum (peripheral) and 80mum (area array) I/O pad pitch on the IC, which must be matched by flip-chip interconnection and substrate wiring pad pitch of the same 20-80mum dimension. System on a Package (SOP) technology pioneered by Georgia Tech PRC enables future "mega-function" electronic and bio-electronic systems through ultra-thin film component integration from the current 50/cm2 to over 10000/cm2. This puts added wiring density and performance demands on the substrate. The other driving force in this thesis research is the increasing adoption of high frequency wireless and wired communication pushing the need for package substrate materials that are stable into multiple GHz frequencies. The current state-of-the-art in IC package substrates is at 20mum lines/spaces and 50-60mum microvia diameter using epoxy dielectrics with loss tangent above 0.01. The research targets are to overcome the barriers of current technologies and demonstrate a set of advanced materials and process technologies capable of 5-10mum lines and spaces, and 10-30mum diameter microvias in a multilayer 3-D wiring substrate using 10-25mum thin film dielectrics with loss tangent in the <0.005. The research elements are organized as follows with a clear focus on understanding and characterization of fundamental materials structure-processing-property relationships and interfaces to achieve the next generation targets: (1) Low CTE Core Substrate. (2) Low Loss Dielectrics with 25mum and smaller microvias. (3) Sub-10mum Width Cu Conductors. (4) Integration of the various dielectric and conductor

  11. Resin infiltration transfer technique

    DOEpatents

    Miller, David V.; Baranwal, Rita

    2009-12-08

    A process has been developed for fabricating composite structures using either reaction forming or polymer infiltration and pyrolysis techniques to densify the composite matrix. The matrix and reinforcement materials of choice can include, but are not limited to, silicon carbide (SiC) and zirconium carbide (ZrC). The novel process can be used to fabricate complex, net-shape or near-net shape, high-quality ceramic composites with a crack-free matrix.

  12. Performance Test on Polymer Waste Form - 12137

    SciTech Connect

    Lee, Se Yup

    2012-07-01

    Polymer solidification was attempted to produce stable waste form for the boric acid concentrates and the dewatered spent resins. The polymer mixture was directly injected into the mold or drum which was packed with the boric acid concentrates and the dewatered spent resins, respectively. The waste form was produced by entirely curing the polymer mixture. A series of performance tests was conducted including compressive strength test, water immersion test, leach test, thermal stability test, irradiation stability test and biodegradation stability test for the polymer waste forms. From the results of the performance tests for the polymer waste forms, it is believed that the polymer waste form is very stable and can satisfy the acceptance criteria for permanent disposal. At present, performance tests with full scale polymer waste forms are being carried out in order to obtain qualification certificate by the regulatory institute in Korea. Polymer waste forms were prepared with the surrogate of boric acid concentrates and the surrogate of spent ion exchange resins respectively. Waste forms were also made in lab scale and in full scale. Lab. scale waste forms were directly subjected to a series of the performance tests. In the case of full scale waste form, the test specimens for the performance test were taken from a part of waste form by coring. A series of performance tests was conducted including compressive strength test, thermal stability test, irradiation stability test and biodegradation stability test, water immersion test, leach test, and free standing water for the polymer waste forms. In addition, a fire resistance test was performed on the waste forms by the requirement of the regulatory institute in Korea. Every polymer waste forms containing the boric acid concentrates and the spent ion exchange resins had exhibited excellent structural integrity of more than 27.58 MPa (4,000 psi) of compressive strength. On thermal stability testing, biodegradation

  13. Synchrotron Radiation Investigation in Epoxy Resin Modified with Polysiloxane System

    NASA Astrophysics Data System (ADS)

    Gan, Wenjun; Li, Weizhen; Ding, Jindian; Gu, Xiaodan; Wang, Cheng

    2014-03-01

    Epoxy resins are one of the most important classes of thermosetting polymers. Epoxy resin modified with polysiloxane is expected that the siloxane moiety may exert its qualities of thermal stability, impact toughness and surface-modification properties. Our group tried to introduce polysiloxane into epoxy resin by blending diglycidyl-ether of bisphenol-A with epoxypropoxypropyl terminated polydimethyl-siloxane and polyetherimide-siloxane in different proportion. These polysiloxane modified epoxy resins have been investigated using a combination of small- and wide angle X-ray scatterings (SAXS and WAXS) and scanning transmission soft X-ray microscopy (STXM). Nano- to micro-scale domain size, distribution and chemical composition were observed with spatial and spectroscopic sensitivities offered by both hard and soft x-ray scattering/microscopy. In-situ SAXS experiments were performed to understand the mechanism of microphase separation and dynamics of nanostructure evolution. Acknowledgment: The authors thank Shanghai Municipal Education Commission (Overseas Visiting Scholar Program 2012) and Shanghai University of Engineering Science (2011xz04) for financial supports.

  14. The many faces of ion-exchange resins

    SciTech Connect

    McNutty, J.T.

    1997-06-01

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

  15. Chemoviscosity modeling for thermosetting resin systems, part 3

    NASA Technical Reports Server (NTRS)

    Hou, T. H.; Bai, J. M.

    1988-01-01

    A new analytical model for simulating chemoviscosity resin 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 (T sub g (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 parameters 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 a 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 transformations of the thermosetting resin systems during cure.

  16. Influence of the resin on interlaminar mixed-mode fracture

    NASA Technical Reports Server (NTRS)

    Johnson, W. S.; Mangalgiri, P. D.

    1985-01-01

    Both literature review data and new data on toughness behavior of seven matrix and adhesive systems in four types of tests were studied in order to assess the influence of the resin on interlaminar fracture. Mixed mode (i.e., various combinations of opening mode 1, G sub 1, and shearing mode 2; G sub 2) fracture toughness data showed that the mixed mode relationship for failure appears to be linear in terms of G sub 1 and G sub 2. The study further indicates that fracture of brittle resins is controlled by the G sub 1 component, and that fracture of many tough resins is controlled by total strain-energy release rate, G sub T. Regarding the relation of polymer structure and the mixed mode fracture: high mode 1 toughness requires resin dilatation; dilatation is low in unmodified epoxies at room temperature/dry conditions; dilatation is higher in plasticized epoxies, heated epoxies, and in modified epoxies; modification improves mode 2 toughness only slightly compared with mode 1 improvements. Analytical aspects of the cracked lap shear test specimen were explored.

  17. Effect of curing environment on mechanical properties and polymerizing behaviour of methyl-methacrylate autopolymerizing resin.

    PubMed

    Ogawa, T; Hasegawa, A

    2005-03-01

    Methyl-methacrylate autopolymerizing resin is used for multiple applications. Therefore, the mechanical properties of autopolymerizing resin should be assessed comprehensively including strength, stiffness and hardness. Any methods that effectively improve these mechanical properties are desirable. The objective of this study is to examine the effects of the curing environment: air or water with/without pressure, and air or water temperature during polymerization, on the strength, stiffness and hardness of autopolymerizing resin. In addition, we examined the polymerizing behaviour associated with the mechanical properties. Autopolymerizing methyl-methacrylate resin (Unifast II) was polymerized under the following conditions: in air and water with/without pressure at 10, 23, 30, 40, 60 and 80 degrees C. The resin specimens were subjected to a transverse test (three-point flexural test) and micro-Brinell surface hardness test. Fractured surfaces of the specimens after the transverse test were examined using a scanning electron microscope (SEM). The transverse strength and transverse modulus increased with increasing curing temperature in both wet and dry conditions. Pressured wet conditions increased transverse strength and transverse modulus over non-pressured wet and dry conditions. The resin polymerized in dry conditions showed higher surface hardness than the one polymerized in wet conditions at matching temperature. The SEM images of fractured surfaces cured at lower temperature exhibited porosity within the polymer base and cracks between the base and poly-methyl-methacrylate (PMMA) particulates. Surfaces of the resin polymerized in wet conditions were characterized with PMMA particulates having rougher surfaces suggestive of water incorporation. Raising temperature and pressuring during polymerization increase strength and stiffness of autopolymerizing resin. However, wet condition reduces surface hardness of resin compared with dry condition. These altered

  18. 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.

  19. Liquid monobenzoxazine based resin system

    DOEpatents

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

    2014-10-07

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

  20. Quaternary ammonium silane-functionalized, methacrylate resin composition with antimicrobial activities and self-repair potential

    PubMed Central

    Gong, Shi-qiang; Niu, Li-na; Kemp, Lisa K.; Yiu, Cynthia K.Y.; Ryou, Heonjune; Qi, Yi-pin; Blizzard, John D.; Nikonov, Sergey; Brackett, Martha G.; Messer, Regina L.W.; Wu, Christine D.; Mao, Jing; Brister, L. Bryan; Rueggeberg, Frederick A.; Arola, Dwayne D.; Pashley, David H.; Tay, Franklin R.

    2012-01-01

    Design of antimicrobial polymers for enhancing healthcare issues and minimizing environmental problems is an important endeavor with both fundamental and practical implications. Quaternary ammonium silane-functionalized methacrylate (QAMS) represents an example of antimicrobial macromonomers synthesized by a sol-gel chemical route; these compounds possess flexible Si-O-Si bonds. In present work, a partially-hydrolyzed QAMS copolymerized with bis-GMA is introduced. This methacrylate resin was shown to possess desirable mechanical properties with both a high degree of conversion and minimal polymerization shrinkage. Kill-on-contact microbiocidal activities of this resin were demonstrated using single-species biofilms of Streptococcus mutans (ATCC 36558), Actinomyces naeslundii (ATCC 12104) and Candida albicans (ATCC 90028). Improved mechanical properties after hydration provided the proof-of-concept that QAMS-incorporated resin exhibits self-repair potential via water-induced condensation of organic modified silicate (ormosil) phases within the polymerized resin matrix. PMID:22659173

  1. Supramolecular Polymers in Aqueous Media.

    PubMed

    Krieg, Elisha; Bastings, Maartje M C; Besenius, Pol; Rybtchinski, Boris

    2016-02-24

    This review discusses one-dimensional supramolecular polymers that form in aqueous media. First, naturally occurring supramolecular polymers are described, in particular, amyloid fibrils, actin filaments, and microtubules. Their structural, thermodynamic, kinetic, and nanomechanical properties are highlighted, as well as their importance for the advancement of biologically inspired supramolecular polymer materials. Second, five classes of synthetic supramolecular polymers are described: systems based on (1) hydrogen-bond motifs, (2) large π-conjugated surfaces, (3) host-guest interactions, (4) peptides, and (5) DNA. We focus on recent studies that address key challenges in the field, providing mechanistic understanding, rational polymer design, important functionality, robustness, or unusual thermodynamic and kinetic properties. PMID:26727633

  2. 21 CFR 177.1340 - Ethylene-methyl acrylate copolymer resins.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ethylene-methyl acrylate copolymer resins. 177.1340 Section 177.1340 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...

  3. 21 CFR 177.1340 - Ethylene-methyl acrylate copolymer resins.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ethylene-methyl acrylate copolymer resins. 177.1340 Section 177.1340 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS...

  4. 21 CFR 177.1340 - Ethylene-methyl acrylate copolymer resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ethylene-methyl acrylate copolymer resins. 177.1340 Section 177.1340 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...

  5. 21 CFR 177.1340 - Ethylene-methyl acrylate copolymer resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... polymer units derived from methyl acrylate. (b) The finished food-contact article, when extracted with the... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ethylene-methyl acrylate copolymer resins. 177.1340 Section 177.1340 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND...

  6. 21 CFR 177.1340 - Ethylene-methyl acrylate copolymer resins.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ethylene-methyl acrylate copolymer resins. 177.1340 Section 177.1340 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS...

  7. 21 CFR 177.1570 - Poly-1-butene resins and butene/ethylene copolymers.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... their characteristic infrared spectra. (ii) Viscosity. Poly-1-butene resins and the butene/ethylene copolymers have an intrinsic viscosity 1.0 to 3.2 as determined by ASTM method D1601-78, “Standard Test Method for Dilute Solution Viscosity of Ethylene Polymers,” which is incorporated by reference....

  8. 21 CFR 177.1570 - Poly-1-butene resins and butene/ethylene copolymers.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... their characteristic infrared spectra. (ii) Viscosity. Poly-1-butene resins and the butene/ethylene copolymers have an intrinsic viscosity 1.0 to 3.2 as determined by ASTM method D1601-78, “Standard Test Method for Dilute Solution Viscosity of Ethylene Polymers,” which is incorporated by reference....

  9. 21 CFR 177.2460 - Poly(2,6-dimethyl-1,4-phenylene) oxide resins.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ...-phenylene) oxide basic resins meet the following: (1) Specifications. Intrinsic viscosity is not less than 0... Solution Viscosity of Vinyl Chloride Polymers,” which is incorporated by reference, modified as follows... reference in paragraph (c)(1) of this section) with the reduced viscosity determined for three...

  10. 21 CFR 177.1570 - Poly-1-butene resins and butene/ethylene copolymers.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... their characteristic infrared spectra. (ii) Viscosity. Poly-1-butene resins and the butene/ethylene copolymers have an intrinsic viscosity 1.0 to 3.2 as determined by ASTM method D1601-78, “Standard Test Method for Dilute Solution Viscosity of Ethylene Polymers,” which is incorporated by reference....

  11. 21 CFR 177.1460 - Melamine-formaldehyde resins in molded articles.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Melamine-formaldehyde resins in molded articles. 177.1460 Section 177.1460 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS...

  12. 21 CFR 177.2710 - Styrene-divinylbenzene resins, cross-linked.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Styrene-divinylbenzene resins, cross-linked. 177.2710 Section 177.2710 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS...

  13. 21 CFR 177.2710 - Styrene-divinylbenzene resins, cross-linked.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Styrene-divinylbenzene resins, cross-linked. 177.2710 Section 177.2710 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS...

  14. 21 CFR 173.70 - Chloromethylated aminated styrene-divinylbenzene resin.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... resin. 173.70 Section 173.70 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) SECONDARY DIRECT FOOD ADDITIVES PERMITTED IN FOOD FOR HUMAN CONSUMPTION Polymer... aqueous dispersion of styrene-divinylbenzene copolymers, first chloromethylated then aminated...

  15. Synthesis and characterization of nanocomposites from amphipathy polyester grafted modified sericite and methylsilicone resin

    NASA Astrophysics Data System (ADS)

    Jiang, B.; Huang, Y. D.; Wang, Q.

    2014-04-01

    The synthetic process of amphipathy polyester grafted modified sericite and methylsilicone resin composites is studied. The analytical results showed that the initial decomposition temperature and the maximum release energy corresponding temperature are enhanced 120 °C and 51 °C. First, modified methylsilicone resin molecular structure is designed. Molecular chair of methylsilicone resin is grafted macromolecular polymer, which is synthesized by toluene-2, 4-diisocyanate modified sericite grafted amphipathy polyester. A modified sericite /methylsilicone resin composites are synthesized through the reaction of functionalized sericite with hydroxyl-terminated methylsilicone resin. X-ray diffraction analysis result showed that the methylsilicone resin has reacted with the modified sericite. Infrared spectra, x-ray photoelectron spectroscopy and nuclear magnetic resonance analysis show that the weak Si-OH band decreases and the strong Si-O-Si band increases. The mechanism of thermal stability is analyzed from the isolated oxygen atom and activated small molecule; interrupted activated Si-OH, steric hindrance. The result of study evidently shows a significant role in enhancing the decomposition temperature of the methylsilicone resin.

  16. Advanced wing design survivability testing and results

    NASA Technical Reports Server (NTRS)

    Bruno, J.; Tobias, M.

    1992-01-01

    Composite wings on current operational aircraft are conservatively designed to account for stress/strain concentrations, and to assure specified damage tolerance. The technology that can lead to improved composite wing structures and associated structural efficiency is to increase design ultimate strain levels beyond their current limit of 3500 to 4000 micro-in/in to 6000 micro-in/in without sacrificing structural integrity, durability, damage tolerance, or survivability. Grumman, under the sponsorship of the Naval Air Development Center (NADC), has developed a high-strain composite wing design for a subsonic aircraft wing using novel and innovative design concepts and manufacturing methods, while maintaining a state-of-the-art fiber/resin system. The current advanced wing design effort addressed a tactical subsonic aircraft wing using previously developed, high-strain wing design concepts in conjunction with newer/emerging fiber and polymer matrix composite (PMC) materials to achieve the same goals, while reducing complexity. Two categories of advanced PMC materials were evaluated: toughened thermosets; and engineered thermoplastics. Advanced PMC materials offer the technological opportunity to take maximum advantage of improved material properties, physical characteristics, and tailorability to increase performance and survivability over current composite structure. Damage tolerance and survivability to various threats, in addition to structural integrity and durability, were key technical issues addressed during this study, and evaluated through test. This paper focuses on the live-fire testing, and the results performed to experimentally evaluate the survivability of the advanced wing design.

  17. Repair bond strength of restorative resin composite applied to fiber-reinforced composite substrate.

    PubMed

    Tezvergil, Arzu; Lassila, Lippo V J; Yli-Urpo, Antti; Vallittu, Pekka K

    2004-02-01

    Delamination or fracture of composite veneers can occur as a result of improper design of the fiber-reinforced composite (FRC) framework. This in vitro study tested the repair bond strength of restorative composite to aged FRC. The substrate was multiphase polymer matrix FRC (everStick) aged by boiling for 8 h and storing at 37 degrees C in water for 6 weeks. The aged substrate surfaces were wet-ground flat with 1200-grit silicon carbide paper and subjected randomly to 5 different surface treatments: 1) An adhesion primer (Composite Activator) and resin (CA), 2) Silane (EspeSil) and resin (SIL-MP), 3) Silane, adhesive primer, and resin (Clearfil Repair) (CF), 4) Air particle-abrading (CoJet), silane, and resin (CJ-SIL-MP), 5) Resin (Scotchbond Multipurpose Resin) only as control (MP). Restorative composite resin (Z250) was added to the substrate in 2 mm layer increments and light-cured. Subsequently, every surface treatment group was divided into 2 subgroups of 12 specimens each. The specimens were either 48 h water-stored or thermocycled (6000 x 5-55 degrees C). The shear bond strengths of composite resin to FRC were measured at a crosshead speed of 1.0 mm/min. The data were analyzed by ANOVA for factors 'treatment type' and 'storage condition'; Tukey's post-hoc tests and Weibull analysis were performed. ANOVA showed a significant difference as a function of surface treatment (P<0.05) and storage condition (P<0.05). The CJ-SIL-MP group showed highest bond strength and Weibull modulus after thermocycling. Repair of multiphase polymer matrix FRC may show reliable bond strength when silane treatment is used along with air-particle abrading. PMID:15124783

  18. Dual resin bonded joints in polyetheretherketone (PEEK) matrix composites

    NASA Astrophysics Data System (ADS)

    Zelenak, Steve; Radford, Donald W.; Dean, Michael W.

    1993-04-01

    The paper describes applications of the dual resin (miscible polymer) bonding technique (Smiley, 1989) developed as an alternative to traditional bonding approaches to joining thermoplastic matrix composite subassemblies into structures. In the experiments, the performance of joint geometries, such as those that could be used to assemble large truss structures in space, are investigated using truss joint models consisting of woven carbon fiber/PEEK tubes of about 1 mm wall thickness. Specific process conditions and hand-held hardware used to apply heat and pressure were chosen to simulate a field asembly technique. Results are presented on tube/cruciform double lap shear tests, pinned-pinned tube compression tests, and single lap shear bond tests of joints obtained using the dual resin bonding technique.

  19. Microwave dielectrometry measurements of glass reinforced polyester resins

    SciTech Connect

    Schlegel, J.L.; Wagner, J.W.; Green, R.E. Jr.

    1999-10-01

    This study describes measurements of dielectric constant as a function of glass reinforcement concentration in polyester resins to use as a control parameter for online process monitoring. Microwave interferometers were constructed in the X and V bands at 9.35 and 60 GHz in both homodyne and heterodyne configurations to measure the phase difference associated with the material. This phase difference is then used to calculate the real part of the dielectric constant from the index of refraction at a microwave frequency. The homodyne X and V band measurements yielded a linear between phase difference and glass concentration. Heterodyne V band measurements produced a nonlinear relationship. Further investigation into the microscopic interactions between the reinforcement particle and the polymer resin is necessary to determine how different concentrations affect the bulk macroscopic material properties.

  20. Polymer nanocomposites for high-temperature composite repair

    SciTech Connect

    Sheng, Xia

    2008-01-01

    A novel repair agent for resin-injection repair of advanced high temperature composites was developed and characterized. The repair agent was based on bisphenol E cyanate ester (BECy) and reinforced with alumina nanoparticles. To ensure good dispersion and compatibility with the BECy matrix in nanocomposites, the alumina nanoparticles were functionalized with silanes. The BECy nanocomposites, containing bare and functionalized alumina nanoparticles, were prepared and evaluated for their thermal, mechanical, rheological, and viscoelastic properties. The monomer of BECy has an extremely low viscosity at ambient temperature, which is good for processability. The cured BECy polymer is a highly cross-linked network with excellent thermal mechanical properties, with a high glass transition temperature (Tg) of 270 C and decomposition temperature above 350 C. The incorporation of alumina nanoparticles enhances the mechanical and rheological properties of the BECy nanocomposites. Additionally, the alumina nanoparticles are shown to catalyze the cure of BECy. Characterization of the nanocomposites included dynamic mechanical analysis, differential scanning calorimetry, thermogravimetric analysis, rheological and rheokinetic evaluation, and transmission electron microscopy. The experimental results show that the BECy nanocomposite is a good candidate as repair agent for resin-injection repair applications.