نتایج جستجو برای: Vinyl chloride-co-Vinyl acetate
تعداد نتایج: 468640 فیلتر نتایج به سال:
the thermal decomposition of 86 % vinyl chloride 14 % vinyl acetate copolymer wasstudied by the conductometry technique in the presence of nitrogen. the kinetics of stability andthermal degradation of vinyl chloride- co- vinyl acetate (pvc- co- pvac) copolymer withcopper, copper oxide and tricalcium dicitrate (st) were investigated at various temperatures (150-180 oc ) in solution. the rate coe...
The thermal decomposition of 86 % vinyl chloride 14 % vinyl acetate copolymer wasstudied by the conductometry technique in the presence of nitrogen. The kinetics of stability andthermal degradation of vinyl chloride- co- vinyl acetate (PVC- co- PVAc) copolymer withcopper, copper oxide and tricalcium dicitrate (st) were investigated at various temperatures (150-180 oC ) in solution. The rate coe...
Vinyl acetate is a colorless, flammable liquid that also has a characteristic smell that can quickly become irritating. This monomer is used principally in the production of polyvinyl acetate (PVAc) and other vinyl acetate co-polymers. Polyvinyl acetate is a precursor of polyvinilyc alcohol and polyvinyl acetate resins (PVA). Vinyl acetate is also copolymerized as a minor raw material for vinyl...
PhD “The role of intumescent flame retardants on the fire behavior of poly(vinyl acetate) and poly(ethylene-co-vinyl acetate): a mechanistic and kinetic study.”
poly(vinyl acetate) is synthesized via solution polymerization, and then it is converted to poly(vinyl alcohol) by alkaline alcoholysis. the aim of the work study was to investigate statistically the influence of reaction variables in vinyl acetate polymerization, the conversion of this monomer to polymer, degree of branching of acetyl group in poly(vinyl acetate), as well as the molecular wei...
Azines made by the reaction of hydrazine with ortho-formylbenzoic acid react with 1,2-diphosphinobenzene and either succinyl chloride or phthaloyl chloride in ca. 30% yield to give rac-bis-3,4-diazaphospholanes bearing benzoic acid groups in the 2 and 5 positions. Condensation of the benzoic acid functionalities with enantiomerically pure amines affords diastereomeric benzoamides which can be s...
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