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Bonding, plasticity affected

Bond density surfaces are also superior to conventional models when it comes te describing chemical reactions. Chemical reactions can involve many changes in chemica bonding, and conventional formulas are not sufficiently flexible to describe what happen (conventional plastic models are even worse). For example, heating ethyl fonnate t( high temperatures causes this molecule to fragment into two new molecules, foraii( acid and ethene. A conventional formula can show which bonds are affected by ths reaction, but it cannot tell us if these changes occur all at once, sequentially, or in soms other fashion. [Pg.26]

Products comprising hydrophilic polymers dissolved in water are well-known and used widely as adhesives but are of little general significance for bonding plastics. The present chapter is concerned only with products based on polymer dispersions, which consist of small discrete particles of diameter about one micron (1 pm, or 10-3 mm) suspended in a continuous water phase. In most instances a protective colloid is present at the interface between the particles of polymer and the water and this helps to stabilize the dispersion and prevent premature coalescence of particles. Dispersions such as these are known as oil-in-water types. With them, the molar mass of the polymer species comprising the dispersed particles does not affect the viscosity and so polymers of high molecular weight can be applied in this way. [Pg.95]

However, often the temperature required to cure the adhesive will adversely affect heat-sensitive plastic parts. Also, heat-curing adhesives are generally more rigid than those that cure at room temperature, and the resulting modulus is too high for many plasticbonding applications. As a result, most adhesives recommended for bonding plastic substrates cure at room temperature. [Pg.452]

Film and coating fonnation occurs when biopolymer molecules interact through cohesive forces, named H-bonding, ionic bonds and covalent bonds (disulfide bonds). Factors affecting film strength are the chemical nature of the biopolymer and the rest of the components of the formulation (plasticizer type and amount and food additives), and the film forming process. [Pg.178]

Always attempt to obtain as much information as possible about temperatures, fluids, pressures, bonding, abrasion, coefficient of fiiction, and a myriad of other factors in order to develop the best formulation. Be sure that the plasticizers are compatible with the NBR at the levels needed, using two or even three different types if necessary to prevent bleeding or exuding that may interfere with bonding or affect the coefficient of friction. Additionally, consider the possible affect of the plasticizer on any plastic (crazing of acrylic or migration into PVC or ABS) or metal or wood that will be in contact with the part. [Pg.72]

Finally mention may be made about the influence of humidity on the electrical insulating properties of plastics. Once again the polymers may be classified into two groups, those which do not absorb water and those which do. The nonabsorbent materials are little affected by humidity whereas the insulation characteristics of the absorbent materials deteriorate seriously. These latter materials are generally certain polar materials which all appear capable of forming some sort of bond, probably a hydrogen bond, with water. Three reasons may be given for the deleterious effects of the water. [Pg.117]

Plasticizers soften the film and increase the adhesion and the setting speed. The most common are phthalates, adipates and benzoates. The amount added can be in a broad range of 10-50%. They affect the swelling and softening of the PVAc emulsion particles, ensure film formation at room temperature, and the tack of the still wet adhesive. They also provide improved moisture resistance of the bond. Disadvantages are the lower resistance of the bond line against heat, possible migration of the plasticizers and enhanced cold flow. [Pg.1078]

Weathering. This generally occurs as a result of the combined effect of water absorption and exposure to ultra-violet radiation (u-v). Absorption of water can have a plasticizing action on plastics which increases flexibility but ultimately (on elimination of the water) results in embrittlement, while u-v causes breakdown of the bonds in the polymer chain. The result is general deterioration of physical properties. A loss of colour or clarity (or both) may also occur. Absorption of water reduces dimensional stability of moulded articles. Most thermoplastics, in particular cellulose derivatives, are affected, and also polyethylene, PVC, and nylons. [Pg.27]

The polymerization rate was essentially zero in each of the systems (even with unreacted double bonds present and continued initiation) after 9 minutes of exposure to UV light. The maximum functional group conversion reached in each system was 96% (1 wt% 1651), 87% (0.5 wt% 1651), and 83% (0.1 wt% 1651). If equal reactivity of the double bonds is assumed, only between 0.16 to 2.89% of unreacted monomer will be present at these total double bond conversions. Unreacted monomer can affectively plasticize the polymer network rendering it more pliable and decreasing its mechanical properties, and unreacted monomer may compromise the biocompatible nature of the system if the monomer leaches to a toxic level. Therefore, it is desirable to identify polymerization conditions which maximize the conversion of monomer. [Pg.196]

The changes in fibre flexibility may affect not only the rigidity of the fibre but also the local plasticity of the cell wall, and this may be important in determining the ease with which the inter-fibre hydrogen bonds are formed during drying. Pulp types also differ in... [Pg.79]

Permanence. The permanence of a plasticizer-i.e., its tendency to remain in the plasticized material, depends on the size of the plasticizer molecule and on its rate of diffusion in the polymer. The larger the plasticizer molecule, the lower its vapor pressure, or volatility and, therefore, the greater its permanence. This accounts for the popularity of certain polymeric plasticizers, such as polyesters, in spite of their relatively high price. Other factors, such as polarity and hydrogen bonding, will also, of course, affect the vapor pressure of the plasticizer. [Pg.14]

Fig. 3. Two-dimensional representation of Covalent bond potential energy curve. Subdivided into three regions Elastic region where the curve is symmetric with respect to Ro, Plastic region where the curve is asymmetric and affect only on the side of R greater than the yield stress. Beyond plastic limit the atoms physically breaks away... Fig. 3. Two-dimensional representation of Covalent bond potential energy curve. Subdivided into three regions Elastic region where the curve is symmetric with respect to Ro, Plastic region where the curve is asymmetric and affect only on the side of R greater than the yield stress. Beyond plastic limit the atoms physically breaks away...

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See also in sourсe #XX -- [ Pg.49 , Pg.65 ]




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Plastic bonding

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