Vinyl polymers polyvinyl alcohol

It has been shown that tensile shear and peel strength for several latex polymers (ethylene vinyl acetate, polyvinyl alcohol, ethylene vinyl chloride, polyvinyl chloride, and acrylic) can be significantly increased by the addition of 10 percent by weight of an epoxy emulsion cured with a tertiary amine curing agent.17 The epoxy modification improves the bond strength in all cases. The degree of improvement is dependent on the selection of the latex type and the chemistry of the latex polymer. [Pg.269]

If polyvinyl alcohol is used as the reducing agent and the oxidation is conducted in the presence of vinyl monomer, grafting occurs. This method of grafting yields substantially pure graft copolymers since the free radicals are formed exclusively on the polymer backbone. [Pg.503]

Emulsion polymerization is widely used to produce polymers in the form of emulsions, such as paints and floor polishes. It also used to polymerize many water insoluble vinyl monomers, such as styrene and vinyl chloride. In emulsion polymerization, an agent emulsifies the monomers. Emulsifying agents should have a finite solubility. They are either ionic, as in the case of alkylbenzene sulfonates, or nonionic, like polyvinyl alcohol. [Pg.316]

Polyvinyl alcohol is a main ingredient in latex paints, hairsprays, shampoos, and glues. It forms polymers and copolymers with other monomers, such as vinyl acetate and methyl methacrylate... [Pg.236]

Release of tetracycUne hydrochloride from PCL fibers was evaluated as a means of controlled administration to periodontal pockets (69). Only small amounts of the drug were released rapidly in vitro or in vivo, and poly(ethylene-co-vinyl acetate) gave superior results. Because Fickian diffusion of an ionic hydrochloride salt in a UpophiUc polymer is unlikely, and because PCL and EVA have essentially identical Fickian permeabilities, we attribute this result to leaching of the charged salt by a mechanism similar to release of proteins from EVA (73). Poly-e-caprolactone pellets have been found unsuitable for the release of methylene blue, another ionic species (74,75). In this case, blending PCL with polyvinyl alcohol (75% hydrolyzed) increased the release rate. [Pg.88]

When vinyl flouride is polymerized, a certain percentage of the flourine atoms are found on adjacent carbon atoms. When polyvinyl alcohol made by hydrolyzing polyvinyl acetate was treated with periodic acid by Flory, he found that the molecular weight was greatly reduced, indicating that there were 1,2-glycol units in the chain. But most of the polymers were regular head-to-tail polymers. [Pg.58]

Other vinyl polymers 4.9.1 Polyvinyl alcohol (PVAL or PVOH)... [Pg.336]

Vinyl chloride polymers and copolymers are often referred to as vinyl resins. PVC is the most important member of the vinyl resin family, which includes polyvinyl acetate (PVAC), polyvinyl alcohol (PVA), polyvinylidene chloride (PVdC) and polyvinyl acetal. Almost always the term PVC includes polymers of VCM as well as copolymers that are mostly VCM. [Pg.348]

Similar grafting experiments by the emulsion technique were described (34) in the system vinyl chloride/copolymer butyl methacrylate-methacrylic acid and in the reverse system, and also in the system styrene/polyvinyl chloride. In this last case again as in homogenous medium, the inverse process failed (vinyl chloride on polystyrene). Grafted acrylonitrile copolymers were also prepared in order to improve their dyeability, by polymerizing acrylonitrile in emulsion in the presence of many different polymers as polyvinyl alcohol, polymethacrylamide and polyvinylpyrrolidone (119, 120, 121), polyvinyl acetate and polyacrylic acid (115), wool (224,225), proteins (136), etc. [Pg.185]

In a process related to GTP, aldehydes initiate the polymerization of silyl vinyl ethers and silyl diene ethers. Here the silyl group is present in the monomer and transfers to the aldehyde ended chains regenerating aldehyde ends [17] (Scheme 8). A Lewis acid catalyst is required. terf-Butyldimethylsilyl works best as a transfer group for vinyl ether while trimethylsilyl is suitable for diene ethers [18]. Even though aldol GTP provides a route to polyvinyl alcohol segments in the subsequent block polymer synthesis, the projected cost of the monomers discouraged further research aimed at commercialization. [Pg.7]

Thus these characterization results demonstrate that polymethacrylic acid does not function in the same manner as polyvinyl alcohol in the emulsion polymerization of vinyl acetate and that the adsorbed polymethacrylic acid can be separated from the bulk polymer, thus distinguishing it from grafted polymer. [Pg.86]

Vinyl Acetate A monomer is a chemical building block used to manufacture a wide variety of polymers including polyvinyl acetate polyvinyl alcohol polyvinyl acetals ethylene vinyl acetate and ethylene vinyl alcohol. [Pg.28]

Polyvinyl alcohol is a vinyl polymer with a carbon-carbon backbone similar to other polymers such as polyethylene and polystyrene and is widely used as a water-soluble biodegradable polymer in the manufacture of delivery systems for fertilizers, pesticides and herbicides and is also used to manufacture containers and films. To date, only bacteria have been described as causing biodegradation of polyvinyl alcohols with some causing complete degradation of the polymer (see Shimao, 2001 for review). [Pg.225]

Polyvinyl alcohol (PVA) is a water-soluble polymer with a glass transition temperature, T, of 80 °C. Although its name implies a homopolymer stmcture, the structure of commercial PVA is a copolymer of vinyl alcohol and vinyl acetate as seen in Fig. 4.2. PVA is made by the incomplete hydrolysis of polyvinyl acetate... [Pg.44]

A significant number of works are concerned with the development of new membranes for the separation of mixtures of aromatic/alicyclic hydrocarbons [10,11,77-109]. For example, the following works can be mentioned. A mixture of cellulose ester and polyphosphonate ester (50 wt%) was used for benzene/cyclohexane separation [113]. High values of the separation factor and flux were achieved (up to 2 kg/m h). In order to achieve better fluxes and separation factors the attention was shifted to the modification of polymers by grafting technique. Grafted membranes were made of polyvinylidene fluoride with 4-vinyl pyridine or acrylic acid by irradiation [83]. 2-Hydroxy-3-(diethyl-amino) propyl methacrylate-styrene copolymer membranes with cyanuric chloride were prepared, which exhibited a superior separation factor /3p= 190 for a feed aromatic component concentration of 20 wt%. Graft copolymer membranes based on 2-hydroxyethyl methylacrylate-methylacrylate with thickness 10 pm were prepared [85]. The membranes yielded a flux of 0.7 kg/m h (for feed with 50 wt% of benzene) and excellent selectivity. Benzene concentration in permeate was about 100 wt%. A membrane based on polyvinyl alcohol and polyallyl amine was prepared [87]. For a feed containing 10 wt% of benzene the blend membrane yielded a flux of 1-3 kg/m h and a separation factor of 62. [Pg.257]

Aqueous SEC. A number of synthetic polymers require the use of aqueous based mobile phase systems for separation/characterisation. These inelude polyacrylamides, polyvinyl alcohols, poly(sodium vinyl... [Pg.202]

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