Vinyl acetate determination

Copolymers of VF and a wide variety of other monomers have been prepared (6,41—48). The high energy of the propagating vinyl fluoride radical strongly influences the course of these polymerizations. VF incorporates well with other monomers that do not produce stable free radicals, such as ethylene and vinyl acetate, but is sparingly incorporated with more stable radicals such as acrylonitrile [107-13-1] and vinyl chloride. An Alfrey-Price value of 0.010 0.005 and an e value of 0.8 0.2 have been determined (49). The low value of is consistent with titde resonance stability and the e value is suggestive of an electron-rich monomer. 

The thermal glass-transition temperatures of poly(vinyl acetal)s can be determined by dynamic mechanical analysis, differential scanning calorimetry, and nmr techniques (31). The thermal glass-transition temperature of poly(vinyl acetal) resins prepared from aliphatic aldehydes can be estimated from empirical relationships such as equation 1 where OH and OAc are the weight percent of vinyl alcohol and vinyl acetate units and C is the number of carbons in the chain derived from the aldehyde. The symbols with subscripts are the corresponding values for a standard (s) resin with known parameters (32). The formula accurately predicts that resin T increases as vinyl alcohol content increases, and decreases as vinyl acetate content and aldehyde carbon chain length increases. 

Suspension Polymerization. At very low levels of stabilizer, eg, 0.1 wt %, the polymer does not form a creamy dispersion that stays indefinitely suspended in the aqueous phase but forms small beads that setde and may be easily separated by filtration (qv) (69). This suspension or pearl polymerization process has been used to prepare polymers for adhesive and coating appHcations and for conversion to poly(vinyl alcohol). Products in bead form are available from several commercial suppHers of PVAc resins. Suspension polymerizations are carried out with monomer-soluble initiators predominantly, with low levels of stabilizers. Suspension copolymerization processes for the production of vinyl acetate—ethylene bead products have been described and the properties of the copolymers determined (70). Continuous tubular polymerization of vinyl acetate in suspension (71,72) yields stable dispersions of beads with narrow particle size distributions at high yields. 

The viscosity of an adhesive directly influences its penetration into a substrate as the viscosity increases, the penetrating power decreases. It also determines the amount of mileage or spread that can be obtained. An optimum viscosity exists for each substrate and each set of machine conditions and must be achieved in order to manufacture an efficient adhesive. Poly(vinyl acetate) emulsions are frequently too low in viscosity to be metered efficiently or to perform well as adhesives by themselves. They must be bodied to working viscosities, eg, by adding thickeners. 

The variable that has the most significant impact on the economics of an extractive distillation is the solvent-to-feed (S/F) ratio. For closeboiling or pinched nonazeotropic mixtures, no minimum-solvent flow rate is required to effect the separation, as the separation is always theoretically possible (if not economical) in the absence of the solvent. However, the extent of enhancement of the relative volatihty is largely determined by the solvent concentration and hence the S/F ratio. The relative volatility tends to increase as the S/F ratio increases. Thus, a given separation can be accomplished in fewer equihbrium stages. As an illustration, the total number of theoretical stages required as a function of S/F ratio is plotted in Fig. 13-75 7 for the separation of the nonazeotropic mixture of vinyl acetate and ethyl acetate using phenol as the solvent. 

Free-radical copolymerization of vinyl acetate with various vinyl siloxane monomers was described 345). Reactions were conducted in benzene at 60 °C using AIBN as the initiator. Reactivity ratios were determined. Selective hydrolysis of the vinyl acetate units in the copolymer backbone was achieved using an aqueous sodium hy-droxide/THF mixture. The siloxane content and degree of hydrolysis were determined by H-NMR. 

A superficially related dependence of on the medium has been observed by Norrish and Smith working with methyl methacrylate, and by Burnett and Melville with vinyl acetate. Rates in poor solvents are high, and determination of by the rotating sector method reveals what appears to be a decrease in kt in the poor solvents. This apparent decrease in kt accounts for the increased rate of polymerization. Actually, precipitation of the polymer seems to be responsible for the effect. The growing radicals become imbedded in precipitated droplets, presumably of very small size. The termination reaction is suppressed owing to isolation of the chain radical in one droplet from that in another. This gel effect is fairly common in systems yield-... 

Mori, S., Determination of the composition and molecular-weight distribution of a poly(vinyl chloride-vinyl acetate) co-polymer by gel permeation chromatography and infrared spectroscopy, ]. Chromatogr., 157, 75, 1978. 

Many analytical techniques are in use for the qualitative and quantitative evaluation of monomers and oligomers extracted from PA6 (GC, differential refrac-tometry, IR, PC, SEC, HPLC, RPLC, etc.). FTIR has been used for quantitative analysis of caprolactam oligomer content (extract %) in polyamide-6 [113], The method, which involves a 3h extraction in boiling methanol, is suitable for process control and plant environment. Kolnaar [114] has used FTIR characterisation of fractional extracts with pentane, hexane, and heptane of HDPE for blow moulding applications. Vinyl acetate in packaging film has similarly been determined by quantitative FUR. 

Much work on the preparation of nonaqueous polymer dispersions has involved the radical polymerization of acrylic monomers in the presence of copolymers having the A block the same as the acrylic polymer in the particle core 2). The preparation of polymer dispersions other than polystyrene in the presence of a PS-PDMS diblock copolymer is of interest because effective anchoring of the copolymer may be influenced by the degree of compatibility between the PS anchor block and the polymer molecules in the particle core. The present paper describes the interpretation of experimental studies performed with the aim of determining the mode of anchoring of PS blocks to polystyrene, poly(methyl methacrylate), and poly(vinyl acetate) (PVA) particles. 

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. 

ISO 4613-1 1993 Plastics - Ethylene/vinyl acetate (E/VAC) moulding and extrusion materials - Part 1 Designation and specification ISO 4613-2 1995 Plastics - Ethylene/vinyl acetate (E/VAC) moulding and extrusion materials - Part 2 Preparation of test specimens and determination of properties ISO 8985 1998 Plastics - Ethylene/vinyl acetate copolymer (EVAC) thermoplastics -Determination of vinyl acetate content... 

The lARC has determined that there is limited evidence in experimental animals and inadequate evidence in humans for the carcinogenicity of vinyl acetate. ... 

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