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Polymeric components

SAN resins themselves appear to pose few health problems in that they have been approved by the EDA for beverage botde use (149). The main concern is that of toxic residuals, eg, acrylonitrile, styrene, or other polymerization components such as emulsifiers, stabilizers, or solvents. Each component must be treated individually for toxic effects and safe exposure level. [Pg.197]

Crosslinkers Acetoxy Si(OOCCH3)3 Alkoxy Si(OR)j Oxime Si(ON=CRR ).3 Amine Si(NHR)j Crosslinking of the polymeric component provide network strucmre. [Pg.701]

In a fundamental sense, the miscibility, adhesion, interfacial energies, and morphology developed are all thermodynamically interrelated in a complex way to the interaction forces between the polymers. Miscibility of a polymer blend containing two polymers depends on the mutual solubility of the polymeric components. The blend is termed compatible when the solubility parameter of the two components are close to each other and show a single-phase transition temperature. However, most polymer pairs tend to be immiscible due to differences in their viscoelastic properties, surface-tensions, and intermolecular interactions. According to the terminology, the polymer pairs are incompatible and show separate glass transitions. For many purposes, miscibility in polymer blends is neither required nor de-... [Pg.649]

The PBAs [55], however, must be distinguished from polymeric components that are defined as follows ... [Pg.650]

After a temptative structure-based classification of different kinds of polymorphism, a description of possible crystallization and interconversion conditions is presented. The influence on the polymorphic behavior of comonomeric units and of a second polymeric component in miscible blends is described for some polymer systems. It is also shown that other characterization techniques, besides diffraction techniques, can be useful in the study of polymorphism in polymers. Finally, some effects of polymorphism on the properties of polymeric materials are discussed. [Pg.183]

Amylopectin is the polymeric component of starch and consists mainly of glucose units joined at the 1,4-positions. Relative molar mass tends to be very high, e.g. between 7 and 70 million. A variety of modified starches are used commercially which are produced by derivatisation to give materials such as ethanoates (acetates), phosphates, and hydroxyalkyl ethers. Modified and unmodified starches are used in approximately equal tonnages, mainly in papermaking, paper coatings, paper adhesives, textile sizes, and food thickeners. [Pg.19]

Initially, the co-agents were mixed with PVDF and FMVQ separately and the mixtures were subjected to mild irradiation. Solubility tests indicated no cross-hnking during this operation. The polymeric components were then mixed in the presence of CaO/MgO in a Brabender plasticorder at a rotor speed of 60 rpm at 160°C. Subsequently, the temperature was lowered to 130°C and a 0.2% benzoyl peroxide paste was added. Mixing was continued for 10 more minutes. Cure characteristics... [Pg.334]

Polymerized components will present an explosion hazard in open air. [Pg.30]

Principles and Characteristics A first step in additive analysis is the identification of the matrix. In this respect the objective for most polymer analyses for R D purposes is merely the definition of the most appropriate extraction conditions (solvent choice), whereas in rubber or coatings analysis usually the simultaneous characterisation of the polymeric components and the additives is at stake. In fact, one of the most basic tests to carry out on a rubber sample is to determine the base polymer. Figure 2.1 shows the broad variety of additive containing polymeric matrices. [Pg.30]

A common technique used for polyolefin samples is to dissolve the sample using solvents such as xylene, decalin, toluene and di- or trichlorobenzene heated to temperatures as high as 130-150°C. After the plastic sample has been solvated, the polymeric component is precipitated by cooling and/or by adding a cold nonsolvent such as acetone, methanol or isopropanol. Polypropylene does not completely dissolve in toluene under reflux for 0.5 to 1 h with magnetic stirring (typically, 2g of polymer in 40 mL of toluene), yet the additives may be extracted [603]. In addition to additives, most solvents also extract some low-MW polymer with subsequent contamination of the extract. To overcome this a procedure for obtaining polymer-free additive extracts from PE, PP and PS has been described based on low-temperature extraction with n-hexane at 0°C [100],... [Pg.149]

Mass analysis of polymer/additive extracts (i.e. without the polymeric component, see Chapter 6) is obviously... [Pg.701]

Tor instance crystalline phase, amorphous phase, hard phase, soft phase, phases formed by different polymeric components in blends or block copolymers. [Pg.134]

The DEP ends with a filament wire onto which a drop of sample is deposited. After evaporation to dryness, the probe is introduced into the source of the mass spectrometer and is rapidly heated to a temperature that can reach 1000°C. This probe is ideal for the study of high molecular weight or polymeric components. It is mostly dedicated to the analysis of samples in the liquid state. Although a small solid fragment of matter may be placed on the filament, this critical operation may lead to the loss of the sample, especially if it is particularly small. To avoid such a difficult handling, the sample may be ground and homogenised in a mini-mortar and then made into suspension with a few drops of appropriate solvent (Scalarone et al., 2003). [Pg.101]

M. Regert, S. N. Dudd, P. F. van Bergen, P. Petrequin and R. P. Evershed, Investigations of both extractable and insoluble polymeric components organic residues in Neolithic ceramic vessels from Chalain (Jura, France), British Archaeological Reports, S939, 78 90 (2001b). [Pg.128]

Many of the physical, chemical and biological properties of wood can be understood by referring to the polymeric chemical constituents. In many cases of wood modification, these polymeric components are modified to some extent. The three structural polymeric components of the wood cell wall are cellulose, hemicellulose and lignin. There are many excellent texts describing the structure and function of these components, and only a brief account is given here. [Pg.25]

When dimensional stability is achieved due to cell wall bulking, the dimensional stabilization achieved is equal to the volume of the water-saturated sample minus the volume of the modified wood. Another class of modification reaction is due to cross-linking between the cell wall polymeric components. In this case, dimensional stability is imparted to the modified wood because movement of the cell wall is restrained, although the volume of the cell wall occupied by the modifying agent may still have an influence (Figure 2.9c). Ohmae etal. (2002) have suggested a method by which the various mechanisms can be... [Pg.35]

The synthetic polymeric components as well as their combinations with proteins such as human serum albumin (HSA), bovine serum albumin (BSA), human serum albumin/a-interferon mixtures (HSA-IFNa) and myoglobin (MYO) did not give any negative response to in vitro and in vivo biocompatibility tests, such as platelet aggregation, complement activation, acute toxicity, and acute thromboembolic potential. [Pg.70]

Techniques commonly used to produce fibrous webs include the wet laid, dry laid carded, and meltblown processes. The wet laid or paper making process is the predominant method for several reasons. The wet laid process, configured properly, allows for the blending of cellulosic and polymeric components. Also, the ability to use short cut length and fine denier fiber provides for consistent blending, uniform formation, and controlled pore structure. [Pg.207]

The anaerobic biological conversion of the major polymeric components of MSW identified require appropriate microorganisms and hydrolytic enzyme systems. Extracellular hydrolytic enzymes, such as cellulases and lipases, have been shown to be effective in the post hydrolysis of anaerobic digester efQuent solids 34) or pretreatment of complex organic polymers before the digestion process 48),... [Pg.26]

Crosslinked polymers are widely used as dental materials (1-31. Perhaps the most challenging application is in the restoration of teeth (4). The monomers must be non-toxic and capable of rapid polymerization in the presence of oxygen and water. The products should have properties comparable to tooth enamel and dentin and a service life of more than a few years. In current restorative materials such properties are sought using so-called "dental composites" which contain high volume fractions of particulate Inorganic fillers (5-71. However in the present article attention is concentrated on one commonly used crosslinked polymeric component, and on the way in which some of its properties are influenced by low volume fractions of fillers. [Pg.427]

Note 6 The number of polymeric components which comprises a blend is often designated by an adjective, viz., binary, ternary, quaternary. [Pg.187]

Note 3 For a mixture containing or consisting of polymeric components, these may be different polymers or species of different molar mass of the same polymer. [Pg.196]

Note 4 The use of the term polymer alloy for a polymer blend is discouraged, as the former term includes multiphase copolymers but excludes incompatible polymer blends. Note 5 The number of polymeric components which comprise a blend is often designated by an adjective, viz. binary, ternary, quaternary, etc. [Pg.225]


See other pages where Polymeric components is mentioned: [Pg.130]    [Pg.328]    [Pg.71]    [Pg.513]    [Pg.298]    [Pg.298]    [Pg.554]    [Pg.557]    [Pg.611]    [Pg.130]    [Pg.281]    [Pg.373]    [Pg.556]    [Pg.351]    [Pg.563]    [Pg.148]    [Pg.162]    [Pg.446]    [Pg.198]    [Pg.38]    [Pg.65]    [Pg.88]    [Pg.104]    [Pg.104]    [Pg.22]    [Pg.271]   


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