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N-Vinyl 2-pyrrolidone

Guner A. and Kara M. Cloud points and temperatures of aqueous poly(N-vinyl-2-pyrrolidone) solutions in the presence of denaturing agents. Polymer 39, 8 9, 1569-1572,1998. [Pg.113]

Copolymers of N-Vinyl-2-pyrrolidone and Sodium-2-acrylamido-2-methylpropane Sulfonate... [Pg.49]

Homopolymers and copolymers from amido-sulfonic acid or salt containing monomers can be prepared by reactive extrusion, preferably in a twin screw extruder [1660]. The process produces a solid polymer. Copolymers of acrylamide, N-vinyl-2-pyrrolidone, and sodium-2-acrylamido-2-methyl-propane sulfonate have been proposed to be active as fluid loss agents. Another component of the formulations is the sodium salt of naphthalene formaldehyde sulfonate [207]. The fluid loss additive is mixed with hydraulic cements in suitable amounts. [Pg.49]

A fluid loss additive for hard brine environments has been developed [1685], which consists of hydrocarbon, an anionic surfactant, an alcohol, a sulfonated asphalt, a biopolymer, and optionally an organophilic clay, a copolymer of N-vinyl-2-pyrrolidone and sodium-2-acrylamido-2-methylpropane sulfonate. Methylene-bis-acrylamide can be used as a crosslinker [1398]. Crosslinking imparts thermal stability and resistance to alkaline hydrolysis. [Pg.49]

The nonionic monomer can be acrylamide, N,N-dimethylacrylamide, N-vinyl-2-pyrrolidone, N-vinyl acetamide, or dimethylamino ethyl methacrylate. Ionic monomers are AMPS, sodium vinyl sulfonate, and vinylbenzene sulfonate. The terpolymer should have a molecular weight between 200,000 to 1,000,000 Dalton. [Pg.49]

Figure 17-8. Monomers for synthetic thickeners vinyl phosphonic acid, N-vinyl-2-pyrrolidone, vinyl sulfonic acid. Figure 17-8. Monomers for synthetic thickeners vinyl phosphonic acid, N-vinyl-2-pyrrolidone, vinyl sulfonic acid.
M. Stephens andB. L. Swanson. Drilling mud comprising tetrapolymer consisting of N-vinyl-2-pyrrolidone, acrylamidopropanesulfonic acid, acrylamide, and acrylic acid. Patent US 5135909,1992. [Pg.464]

TP Davis, MB Hughn, DCF Yip. Properties of poly(N-vinyl-2-pyrrolidone) hydrogels crosshnked with ethylene glycol dimethacrylate. Polymer 29 701-706, 1988. [Pg.551]

The behavior of Cu(II)(aq) is relatively more understood than other metal ions. Haas and Gedanken [74] found only a partial reduction of Cu2+ ions to Cu+ (95%) instead of metallic copper (5.1%) in the presence of cetyltrimethylammonium bromide in an ultrasonic field and thus obtained CuBr particles instead of Cu. Nevertheless, when polymers such as poly(N-vinyl 2-pyrrolidone) or poly(vinyl alcohol) were used, the end product was metallic copper particles, as expected. They have proposed the reduction of Cu2+ ions to copper as the first stage, however, in the second stage Cu reacted with OH radicals or H2O2, formed by sonolysis of water to produce Cu+ and OH- ions as under ... [Pg.230]

Finally, these particles generated in ionic liquids are efficient nanocatalysts for the hydrogenation of arenes, although the best performances were not obtained in biphasic liquid-liquid conditions. The main importance of this system should be seen in terms of product separation and catalyst recycling. An interesting alternative is proposed by Kou and coworkers [107], who described the synthesis of a rhodium colloidal suspension in BMI BF4 in the presence of the ionic copolymer poly[(N-vinyl-2-pyrrolidone)-co-(l-vinyl-3-butylimidazolium chloride)] as protective agent. The authors reported nanoparticles with a mean diameter of ca. 2.9 nm and a TOF of 250 h-1 in the hydrogenation of benzene at 75 °C and under 40 bar H2. An impressive TTO of 20 000 is claimed after five total recycles. [Pg.244]

PEG, 13 736-737 pH-sensitive, 13 743 PHEMA, 13 733-734, 749, 750 poly(acrylamide)-based, 13 737-738 poly(acrylic/methacrylic acid), 13 734 poly(N-vinyl 2-pyrrolidone), 13 739 polyurethane, 13 739 porous, 13 750-751 preparation methods for, 13 731-732 properties and preparation of,... [Pg.449]

For the addition of ethylene, EtOAc as solvent was particularly advantageous and gave 418 in 60% yield (Scheme 6.86). The monosubstituted ethylenes 1-hexene, vinylcyclohexane, allyltrimethylsilane, allyl alcohol, ethyl vinyl ether, vinyl acetate and N-vinyl-2-pyrrolidone furnished [2 + 2]-cycloadducts of the type 419 in yields of 54—100%. Mixtures of [2 + 2]-cycloadducts of the types 419 and 420 were formed with vinylcyclopropane, styrene and derivatives substituted at the phenyl group, acrylonitrile, methyl acrylate and phenyl vinyl thioether (yields of 56-76%), in which the diastereomers 419 predominated up to a ratio of 2.5 1 except in the case of the styrenes, where this ratio was 1 1. The Hammett p value for the addition of the styrenes to 417 turned out to be -0.54, suggesting that there is little charge separation in the transition state [155]. In the case of 6, the p value was determined as +0.79 (see Section 6.3.1) and indicates a slight polarization in the opposite direction. This astounding variety of substrates for 417 is contrasted by only a few monosubstituted ethylenes whose addition products with 417 could not be observed or were formed in only small amounts phenyl vinyl ether, vinyl bromide, (perfluorobutyl)-ethylene, phenyl vinyl sulfoxide and sulfone, methyl vinyl ketone and the vinylpyri-dines. [Pg.317]

In a series of papers, Matsuda et al. [291-295] employed RAFT-SIP with immobilized benzyl N,N-diethyldithiocarbamate to form polymer brushes from styrene, methacrylamides, acrylamides and acrylates, NIPAM and N-vinyl-2-pyrrolidone on various surfaces. The SIP is initiated by UV irradiation of the surface-bonded dithiocarbamates. Thermoresponsive polymer brushes were prepared by the polymerization of NIPAM and investigated by XPS, wetting experiments and mainly SPM [294]. Patterned polymer brush layers were also prepared. When chloro-methyl styrene was used as a comonomer, RAFT-SIP resulted in branching. By control of the branching, spatio-resolved hyperbranching of a controllable stem/ branch design was realized (Fig. 9.32) [293, 295]. [Pg.423]

The submitters employed, without purification, N-vInyl-2-pyrrolidone obtained from GAF Corporation,... [Pg.74]

N-Vinyl-2-pyrrolidone 2-Pyrrolidinone, 1-vinyl- (8) 2-Pyrrolidinone, 1-ethenyl- (9) (88-12-0)... [Pg.211]

Poiy(N-vinyl-2-pyrrolidone), PVP Bimetallic Pd-Pt particles Refluxing mixed solutions of palladium(II) chloride and hexachloroplatmicfTV) acid in ethanol-water (1 1, v/v) in the presence of PVP resulted in the formation of well-dispersed, stable, polymer-protected Pd-Pt particles 58... [Pg.212]

Titania and silica glass thin films Au, Pt Photoreduction of HAuCl and K.2PtCl4 in ethanol-water in the presence of poly(N-vinyl-2-pyrrolidone) or poly(methyl vinyl ether led to metal particles (sizes depended on solvent composition the smallest, 2.8 nm in diameter, was obtained in 100% alcohol) which were mixed with Ti(i-OC3H7)4 and acetylacetone under N2. Subsequent to 30 minutes of stirring, exposure to moisture produced Ti02-embedded metal particles 74... [Pg.214]

Process for the Preparation of Amphiphilic Poly(N-vinyl-2-pyrrolidone)... [Pg.486]

Fontana and Thomas25) estimated LH from the sedimentation rate of carbon-black particles covered with poly(lauryl methacrylate) (PLMA) or stearyl methacrylate/N-vinyl-2-pyrrolidone copolymer (PAM/A-VP). The values of LH for PLMA were 20 to 40 A, while those for PAM-VP were 210 40 A. [Pg.46]

The phase separation behavior of a sample of poly(N-vinyl-2.pyrrolidone) (PVP) in aqueous Na2S04 (0.55 M) containing a surfactant, sodium dodecyl sulfate (SDS), was reported [83], This phenomenon was studied in function of temperature and surfactant concentration as independent variables. Without surfactant, the polymer exhibits a lower solution temperature (LCST) of 28°C, above which it precipitates. At SDS concentrations of only 300 mg L-1, aggregation was prevented and the behavior of isolated polymer molecules could be studied. [Pg.26]

Figure 3.3 shows as an example, the surface pressure-area per repeating unit (tt - A) isotherms of Langmuir monolayers obtaining by spreading of poly(N-vinyl-2-pyrrolidone) (PVP) on aqueous Na2SC>4 subphase, for both molecular weights and several temperatures [44],... [Pg.167]


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N-vinylation

Pyrrolidon

Pyrrolidone

Pyrrolidones

Vinyl pyrrolidone

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