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  • 1
    Electronic Resource
    Electronic Resource
    Brookfield, Conn. : Wiley-Blackwell
    Journal of Vinyl and Additive Technology 16 (1994), S. 197-202 
    ISSN: 0193-7197
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The ability of different organic additives to increase the bulk density (BD) and the free flow (FF) of PVC was investigated. PVC was treated by quarternary ammonium salts, low-molecular glycols, polyethylene glycols, polyethylene wax, stearic acid, butyl stearate, oxyethylated fatty acids and alcohol, non-oxyethylated and oxyethylated partial fatty acid esters of polyhydric alcohols. Increasing one of the mentioned values is not always accompanied by increasing the other. There exist additives which increase the BD only, the FF only, and both values simulataneously. The BD of treated PVC is often instable; it may increase and decrease on standing. The additives used do not affect the structure of PVC particles, but may change the volume of external voids between them. The efficiency of each additive depends on its polarity and structure of the chains. The mechanism of the action of additives altering the BD and FF was considered. It was expected that the additives leading to denser packing of the PVC powder reduce the interparticle interaction at the expense of particle-additive interaction.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 181-189 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Vinyl acetate-vinyl alcohol copolymers were fractionated in order to obtain their degree of hydrolysis distributions. In the method employed for fractionation, the differences in molecular weight of copolymer did not affect the fractional separation. Degree of hydrolysis distributions was found to be broad, with a pronounced maximum at a low degree of hydrolysis. Viscosity measurements were performed both for the precipitated fractions and unfractionated polymer. The Huggins constant was found to increase with a decrease in the degree of hydrolysis of polyvinyl acetate. These results were interpreted in terms of a polymer molecular association. From values of Huggins constants, comparative information about copolymer “blockiness” is also established.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 48 (1993), S. 435-442 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Aqueous solutions of partly hydrolyzed polyvinyl acetate (polyvinyl alcohol, PVA) and hydroxypropyl methylcellulose (HPMC) are used together as dispersants in vinyl chloride suspension polymerization. Surface tension, viscosity, and cloud point (CP) of diluted PVA and HPMC solutions at room temperature, viscosity of concentrated solutions as a function of temperature, and incipient gelation temperatures (IGT) were determined. Viscosity measurements show synergism of binary polymer mixtures. The synergetic effect diminishes with rise of temperature. IGT of PVA-HPMC solutions do not differ remarkably from those of solutions containing only HPMC and are much higher than the corresponding CP. At definite relative concentrations of HPMC and PVA, separation of the mixtures into two immiscible phases occurs. Each phase contains both polymers, but in the denser and more concentrated phase (lower layer), PVA is the prevailing component. The mutual influence of the two polymers causes changes in solute-solvent interaction, that is, dehydration of the polymers' molecules. It is assumed that in the processes occurring in the system, preferential molecules of definite structure take part. The merits of a system using both polymers as dispersants in the vinyl chloride polymerization are discussed in the light of ascertained data. © 1993 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Publication Date: 2018
    Description: One of the most prevalent epitranscriptomic modifications is RNA editing. In higher eukaryotes, RNA editing is catalyzed by one of two classes of deaminases: ADAR family enzymes that catalyze A-to-I (read as G) editing, and AID/APOBEC family enzymes that catalyze C-to-U. ADAR-catalyzed deamination has been studied extensively. Here we focus on AID/APOBEC-catalyzed editing, and review the emergent knowledge regarding C-to-U editing consequences in the context of human disease.
    Electronic ISSN: 2073-4425
    Topics: Biology
    Published by MDPI
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