Search NASA⌕ Search

SEARCH · Search NASA

Results for “Copolymerization”

Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 307 records · Page 17

The evolutionary sequence: origin and emergences

The evolutionary sequence is being reexamined experimentally from a "Big Bang"origin to the protocell and from the emergence of protocell and variety of species to Darwin's mental power (mind) and society (The Descent of Man). A most fundamentally revisionary consequence of experiments is an emphasis on endogenous ordering. This principle, seen vividly in ordered copolymerization of amino acids, has had new impact on the theory of Darwinian evolution and has been found to apply to the entire sequence. Herein, I will discuss some problems of dealing with teaching controversial subjects.

Non-NASA Center↗

Protein specific fluorescent microspheres for labelling a protein

Highly fluorescent, stable and biocompatible microspheres are obtained by copolymerizing an acrylic monomer containing a covalent bonding group such as hydroxyl, amine or carboxyl, for example, hydroxyethylmethacrylate, with an addition polymerizable fluorescent comonomer such as dansyl allyl amine. A lectin or antibody is bound to the covalent site to provide cell specificity. When the microspheres are added to a cell suspension the marked microspheres will specifically label a cell membrane by binding to a specific receptor site thereon. The labeled membrane can then be detected by fluorescence of the fluorescent monomer.

Rembaum, Alan↗

Cell specific, variable density, polymer microspheres

Biocompatible polymeric microspheres having an average diameter below about 3 microns and having density at least 15% greater or lesser than organic cells and having covalent binding sites are provided in accordance with this invention. The microspheres are obtained by copolymerizing a hydroxy or amine substituted acrylic monomer such as hydroxyethylmethacrylate with a light or dense comonomer such as a fluoromonomer. A lectin or antibody is bound to the hydroxy or amine site of the bead to provide cell specificity. When added to a cell suspension the marked bead will specifically label the cell membrane by binding to specific receptor sites thereon. The labelled membrane can then be separated by density gradient centrifugation.

Yen, Shiao-Ping S.↗

Cell specific, variable density, polymer microspheres

Biocompatible polymeric microspheres having an average diameter below about 3 microns and having a density at least 15% greater or lesser than organic cells and having covalent binding sites are provided in accordance with this invention. The microspheres are obtained by copolymerizing a hydroxy or amine substituted acrylic monomer such as hydroxyethylmethacrylate with a light or dense comonomer such as a fluoromonomer. A lectin or antibody is bound to the hydroxy or amine site of the bead to provide cell specificity. When added to a cell suspension the marked bead will specifically label the cell membrane by binding to specific receptor sites thereon. The labelled membrane can then be separated by density gradient centrifugation.

Yen, Shiao-Ping S.↗

Norbornene-Based Polymer Electrolytes for Lithium Cells

Norbornene-based polymers have shown promise as solid electrolytes for lithium-based rechargeable electrochemical cells. These polymers are characterized as single-ion conductors. Single-ion-conducting polymers that can be used in lithium cells have long been sought. Single-ion conductors are preferred to multiple-ion conductors as solid electrolytes because concentration gradients associated with multiple-ion conduction lead to concentration polarization. By minimizing concentration polarization, one can enhance charge and discharge rates. Norbornene sulfonic acid esters have been synthesized by a ring-opening metathesis polymerization technique, using ruthenium-based catalysts. The resulting polymer structures (see figure) include sulfonate ionomers attached to the backbones of the polymer molecules. These molecules are single-ion conductors in that they conduct mobile Li+ ions only; the SO3 anions in these polymers, being tethered to the backbones, do not contribute to ionic conduction. This molecular system is especially attractive in that it is highly amenable to modification through functionalization of the backbone or copolymerization with various monomers. Polymers of this type have been blended with poly(ethylene oxide) to lend mechanical integrity to free-standing films, and the films have been fabricated into solid polymer electrolytes. These electrolytes have been demonstrated to exhibit conductivity of 2 10(exp -5)S/cm (which is high, relative to the conductivities of other solid electrolytes) at ambient temperature, plus acceptably high stability. This type of norbornene-based polymeric solid electrolyte is in the early stages of development. Inasmuch as the method of synthesis of these polymers is inherently flexible and techniques for the fabrication of the polymers into solid electrolytes are amenable to optimization, there is reason to anticipate further improvements.

Cheung, Iris↗

Synthesis and polymerization of vinyl triazolium ionic liquids

Herein, we describe polymerized ionic liquids, demonstrate the synthesis of polymerized ionic liquids, and demonstrate the polymerization of triazolium monomers. One embodiment shows the polymeriazation of the triazolium monomers with bis(trifluoromethanesulfonyl)imide anions. In another embodiment we show the feasibility of copolymerizing with commodity monomers such as styrene using free radical polymerization techniques.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Polymers functionalized with bronsted acid groups

Porous aromatic framework polymers functionalized with Bronsted acid moieties are prepared by polymerization of a three-dimensional organic aryl or heteroaryl monomer and its copolymerization with a second aryl or heteroaryl monomer functionalized with one or more Bronsted acid moiety. The polymers are characterized by a stable three-dimensional structure, which, in exemplary embodiments, includes interpenetrating subunits within one or more domain of the bulk polymer structure. The polymers are of use in methods of adsorbing ammonia and amines and in devices and systems configured for this purpose.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Polymers for use as protective layers and other components in electrochemical cells

Electrode structures and electrochemical cells are provided. The electrode structures and/or electrochemical cells described herein may include one or more protective layers comprising a polymer layer and/or a gel polymer electrolyte layer. The polymer layer may be formed from the copolymerization of an olefinic monomer comprising at least one electron withdrawing group and an olefinic comonomer comprising at least one electron donating group. Methods for forming polymer layers are also provided.

Fleischmann, Sven↗

Polymer electrolytes including heteropolyacids

This disclosure provides polymer electrolytes, polymer electrolyte membranes (PEM's) and membrane electrode assemblies (MEA's) such as may be useful in fuel cells which contain or comprise polyoxometalates (POM's) or heteropolyacids (HPA's). In some embodiments the polyoxometalate, it's counterions or both may comprise Mn and/or Ce. In some embodiments the polymer electrolyte is fluorinated. In some embodiments the polymer electrolyte comprises a second acidic functional group other than a polyoxometalate. In another aspect, the present disclosure provides methods of making polymer electrolytes including methods which comprising a step of copolymerizing monomers comprising a covalently bound polyoxometalates and methods which comprise a step of covalently attaching a polyoxometalate to the polymer.

Hamrock, Steven J.↗

Polymers for use as protective layers and other components in electrochemical cells

Electrode structures and electrochemical cells are provided. The electrode structures and/or electrochemical cells described herein may include one or more protective layers comprising a polymer layer and/or a gel polymer electrolyte layer. The polymer layer may be formed from the copolymerization of an olefinic monomer comprising at least one electron withdrawing group and an olefinic comonomer comprising at least one electron donating group. Methods for forming polymer layers are also provided.

Fleischmann, Sven↗

Direct Insertion Polymerization of Ionic Monomers: Rapid Production of Anion Exchange Membranes

The limited number of methods to directly polymerize ionic monomers currently hinders rapid diversification and production of ionic polymeric materials, namely anion exchange membranes (AEMs) which are essential components in emerging alkaline fuel cell and electrolyzer technologies. Herein, we report a direct coordination-insertion polymerization of cationic monomers, providing the first direct synthesis of aliphatic polymers with high ion incorporations and allowing facile access to a broad range of materials. We demonstrate the utility of this method by rapidly generating a library of solution processable ionic polymers for use as AEMs. We investigate these materials to study the influence of cation identity on hydroxide conductivity and stability. Furthermore, we found that AEMs with piperidinium cations exhibited the highest performance, with high alkaline stability, hydroxide conductivity of 87 mS cm –1 at 80 °C, and a peak power density of 730 mW cm –2 when integrated into a fuel cell device.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Thermodynamic characteristics of poly(cyclohexylethylene-b-ethylene-co-ethylethylene) block copolymers

A series of poly(cyclohexylethylene-b-ethylene-co-ethylethylene) (C-E/E{sub E}) diblock copolymers containing approximately 50% by volume glassy C blocks and varying fraction (x) of E{sub E} repeat units, 0.07 {le} x {le} 0.90, was synthesized by anionic polymerization and catalytic hydrogenation. The effects of ethyl branch content on the melt state segment-segment ({chi}) interaction parameter and soft (E/E{sub E}) block crystallinity were studied. The percent crystallinity ranged from approximately 30% at x = 0.07 to 0% at about x {ge} 0.30, while the melting temperature changed from 101 C at x = 0.07 to 44 C at x = 0.28. Dynamic mechanical spectroscopy was employed to determine the order-disorder transition (ODT) temperatures, from which {chi} was calculated assuming the mean-field prediction ({chi}N{sub n}){sub ODT} = 10.5. Previously published results for the temperature dependent binary interaction parameters for C-E (x = 0.07), C-E{sub E} (x = 0.90), and E-E{sub E} (x = 0.07 and x = 0.90) fail to account for the quantitative x dependence of {chi}, based on a simple binary interaction model.

36 MATERIALS SCIENCE↗

Enzymatic synthesis of kraft lignin-acrylate copolymers using an alkaline tolerant laccase

Abstract Softwood kraft lignin is a major bioresource relevant to the production of sustainable bio-based products. Continued challenges to lignin valorization, however, include poor solubility in organic solvents and in aqueous solutions at neutral pH. Herein, an alkaline tolerant laccase was used to graft acrylate functionalities onto softwood kraft lignin, which is expected to enhance the reactivity of lignin with isocyanate when producing bio-based polyurethanes. Proton nuclear magnetic resonance, Fourier-transform infrared spectroscopy, and high-performance liquid chromatography were used to confirm successful grafting of the acrylate monomer onto lignin and verify the importance of including tert-butyl hydroperoxide as an initiator in the grafting reaction. Laccase-mediated grafting of softwood kraft lignin under alkaline conditions produced lignin products with approximately 30% higher hydroxyl value and higher reactivity toward isocyanate. The reported enzymatic and aqueous process presents an opportunity for the sustainable valorization of softwood kraft lignin. Key points • Softwood kraft lignin displayed high phenolic hydroxyl content, polydispersity index and average molecular weight • Grafting hydroxyethyl acrylate (HEA) monomer onto kraft lignin by laccase was successful at 60 °C and alkaline conditions • Lignin-HEA grafted copolymer showed an increase in total OH value and an increase in average molecular weight

59 BASIC BIOLOGICAL SCIENCES↗

Environmentally Responsive Poly(N-isopropylacrylamide)-co-poly(acrylic acid) Hydrogels for Separation of Toxic Metals and Organic Explosive Compounds from Water

Temperature and pH-sensitive hydrogels were prepared from N-isopropyl acrylamide and polyacrylic acid through co-polymerization using ammonium persulfate as the initiator, N,N,N’,N’-tetramethylenediamine as the activator and N,N’-methylene bisacrylamide as crosslinker. The gels were characterized on the basis of FTIR and NMR spectral analysis, SEM micrograms and swelling studies. The effect of pH and temperature on swelling behavior of these gels was investigated. Preliminary batch absorption experiments were conducted to explore the feasibility of separating As(V), Cr(VI), the explosive components cyclotrimethylene-trinitramine (RDX), and cyclotetramethylene-tetranitramine (HMX), from aqueous medium using the hydrogels. The results of the study indicated that the hydrogels prepared are stable and the gels have potential environmental applications for separating pollutants from water.

54 ENVIRONMENTAL SCIENCES↗

Synthesis and study of optical properties of copolymers of perfluoro-2,2-dimethyl-1,3-dioxole and perfluoro(propyl vinyl ether)

Polymerization under ultrahigh pressure without involvement of initiators was used to synthesize amorphous copolymers of perfluoro-2,2-dimethyl-1,3-dioxole and perfluoro(propyl vinyl ether). The copolymers have molecular masses within 2•10{sup 4}—7•10{sup 4} au, possess high optical transparency in the telecom ranges of wavelength at 0.85, 1.3, and 1.5 μm and very low refractive index n = 1.293—1.314 at the wavelength λ = 632.8 nm. They can form films and are promising as claddings for optical fibers and waveguides. Amorphous films with the thickness of 1—4 μm were prepared by spin-coating from solutions of the perfluorinated copolymers in perfluorodecalin.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Novel organic polymer-inorganic hybrid material zinc poly(styrene-phenylvinylphosphonate)-phosphate prepared with a simple method

A novel type of organic polymer-inorganic hybrid material layered crystalline zinc poly(styrene-phenylvinylphosphonate)-phosphate (ZnPS-PVPP) was synthesized under mild conditions in the absence of any template. And the ZnPS-PVPP were characterized by FT-IR, diffusion reflection UV-vis, AAS, N{sub 2} volumetric adsorption, SEM, TEM and TG. Notably, this method was entirely different from the traditional means used for preparing other zinc phosphonate. Moreover, it could be deduced that ZnPS-PVPP possessed the potential applications for catalyst supports. In the initial catalytic tests, the catalysts immobilized onto ZnPS-PVPP showed comparable or higher activity and enantioselectivity with that of catalysts reported by our group in the asymmetric epoxidation of unfunctional olefins. - Graphical Abstract: Zinc poly(styrene-phenylvinylphosphonate)-phosphate was a novel type of layered crystalline organic polymer-inorganic hybrid material prepared under mild conditions without addition of any template and could be used as heterogeneous catalyst supports. Highlights: > New types of layered crystalline inorganic-organic polymer hybrid materials zinc poly(styrene-phenylvinylphosphonate-phosphate(ZnPS-PVPP)). > ZnPS-PVPP prepared under mild condition without adding of any template. > Immobilized chiral salen Mn (III) catalysts on ZnPS-PVPP supports show comparative activity and enantioselectivity with that of on ZSPP or ZPS-PVPA.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Automatic, simultaneous control of polymer composition and molecular weight during free radical copolymer synthesis

Fully automatic, simultaneous control of polymer composition and molecular weight trajectories during free radical copolymer synthesis was achieved by coupling the continuous ACOMP data stream into a feedback controller which operated pumps for reactor feed of comonomers. The controller operates without recourse to a detailed kinetic model or reactivity ratios. Rather, it uses the fact that instantaneous copolymer chain composition is related to the instantaneous rate of consumption of comonomers, and the rate for each of these is described by rates α 1 and α 2 for comonomers 1 and 2, respectively. The instantaneous weight average molecular weight M w,inst is proportional to total comonomer concentration via a constant p. Hence, target trajectories for composition and M w can be independently prescribed and followed. Finally, since α 1 , α 2 and p are directly measurable from the ACOMP data stream, their values can be constantly updated by the automatic controller during the reaction process to insure the target trajectories are followed.

36 MATERIALS SCIENCE↗

Simple Monomers for Precise Polymer Functionalization During Ring-Opening Metathesis Polymerization

Controlling the monomer sequence of synthetic polymers is a grand challenge in polymer science. Conventional sequence control has been achieved in dispersed polymers by exploiting the kinetic tendencies of monomers and their order of addition. While the sequence of blocks in multiblock copolymers can be readily tuned using sequential addition of monomers (SAM), control over the sequence distribution is eroded as the targeted block size approaches a single monomer unit (i.e., X n ~ 1) due to the stochastic nature of chain-growth reactions. Thus, unique monomers are needed to ensure precise single additions. Herein, we investigate common classes of cyclic olefin monomers for ring-opening metathesis polymerization (ROMP) to identify monomers for single unit addition during sequential monomer addition synthesis. Through careful analysis of polymerization kinetics, we find that easily synthesized oxanorbornene imide monomers are suitable for single-addition reactions. With the identified monomers, we demonstrate the synthesis of multiblock copolymers containing up to three precise functionalization sites and singly cross-linked four-armed star copolymers. In conclusion, we envision that expanded kinetic analyses of monomer reactivities in ROMP reactions will enable novel polymer synthesis capabilities such as the autonomous synthesis of sequence-defined polymers or one-shot multiblock copolymer syntheses.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗