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Monomers INDEX

In the systems (I) and (III) 2-simplex consists of a sole cell, all the trajectories inside which approach SP corresponding to homopolymer Ms where rs < 1. The systems (I) and (III) topologically are equivalent, since they differ from each other only by the inversion of the monomer indexes therefore their phase portraits are of the same type, too. In the systems (II) and (IV) the azeotropic point separates the simplex into the two cells. However, the system (IV), in which both parameters r, and r2 exceed unity practically is non-realizable [20-24]. That is why the stable binary azeotropes are excluded from the consideration, and the dynamics of the copolymerization of two monomers is exhaustively characterized by only two types (I) and (II) of phase portraits. [Pg.36]

More recent I inear graphical methods are invariant to the inversion of monomer indexes. One procedure [8] uses the form... [Pg.255]

Fig. 1. CO/ethene-based PK-E. Note Applied notation for perfectly alternating CO/a-olefin polyketones PK-MiM2-re, in which Mi and M2 are abbreviations for the types of a-olefins incorporated in the co- or terpolymer chain [eg M = ethene (E), propene (P), butene (B), pentene (P), hexene (H), octene (0), decene (D), dodecene (Do), tetradecene (Td), hexadecene (Hd), octadecene (Od), icosene (Ic), and styrene (S)] and n, the molar monomer index n = [100 x [M2]/([Mi] + [M2])], is the percentage of M2 (in mol%) on the total amount of a-olefin incorporated in the polymer backbone. For example, PK-E represents a copolymer build up of CO and ethene, while PK-EP-6 represents a terpolymer build up of CO, ethene, and propene in a molar ratio of 100 94 6. Fig. 1. CO/ethene-based PK-E. Note Applied notation for perfectly alternating CO/a-olefin polyketones PK-MiM2-re, in which Mi and M2 are abbreviations for the types of a-olefins incorporated in the co- or terpolymer chain [eg M = ethene (E), propene (P), butene (B), pentene (P), hexene (H), octene (0), decene (D), dodecene (Do), tetradecene (Td), hexadecene (Hd), octadecene (Od), icosene (Ic), and styrene (S)] and n, the molar monomer index n = [100 x [M2]/([Mi] + [M2])], is the percentage of M2 (in mol%) on the total amount of a-olefin incorporated in the polymer backbone. For example, PK-E represents a copolymer build up of CO and ethene, while PK-EP-6 represents a terpolymer build up of CO, ethene, and propene in a molar ratio of 100 94 6.
Study the distribution of counterions along the chain for different values of and Iq. Besides the monomer index i, another quantity can be used to set the location of a given monomer in the chain. This is the contour length Lc(0 = ( l) o which gives an interesting alternative interpretation. The condensation degree 0, as a function of monomer index i and the contour length Lc for different values of and lo is shown in Fig. 8. [Pg.373]

Fig. 8 Degree of counterion condensation 0, as a function of (a) monomer index i, for chains with Iq = 0.25 nm and different polymerization degrees and (b) the contour length Lc(i), for a chain with 30 charged monomers empty symbol) and chain with 30 charged monomers +1 neutral monomer (filled symbol)... Fig. 8 Degree of counterion condensation 0, as a function of (a) monomer index i, for chains with Iq = 0.25 nm and different polymerization degrees and (b) the contour length Lc(i), for a chain with 30 charged monomers empty symbol) and chain with 30 charged monomers +1 neutral monomer (filled symbol)...
Polymers for improving the viscosity index of the copolymethacrylate type can be made into dispersants by copolymerization with a nitrogen monomer. The utilization of these copoiymers allows the quantity of dispersant additives in the formulation to be reduced. [Pg.361]

The major use of vinylpyrrohdinone is as a monomer in manufacture of poly(vinylpyrrohdinone) (PVP) homopolymer and in various copolymers, where it frequendy imparts hydrophilic properties. When PVP was first produced, its principal use was as a blood plasma substitute and extender, a use no longer sanctioned. These polymers are used in pharmaceutical and cosmetic appHcations, soft contact lenses, and viscosity index improvers. The monomer serves as a component in radiation-cured polymer compositions, serving as a reactive diluent that reduces viscosity and increases cross-linking rates (see... [Pg.114]

Polymer Monomer CAS Registry r Density, Refractive index. [Pg.162]

Numerous methods for the deterrnination of monomer purity, including procedures for the deterrnination of saponification equivalent and bromine number, specific gravity, refractive index, and color, are available from manufacturers (68—70). Concentrations of minor components are deterrnined by iodimetry or colorimetry for HQ or MEHQ, by the Kad-Eisher method for water, and by turbidity measurements for trace amounts of polymer. [Pg.165]

When exposed to light, the monomeric material in the photopolymers or photothermoplasts polymerizes, thus locally increasing density and index of refraction. A subsequent fixation process polymerizes the monomer throughout the polymer matrix. [Pg.154]

Monomer Molecular weight Boiling point, °C Melting point, °C Refractive index, Density, g/cm ... [Pg.426]

Monomers such as methyl methacrylate [80-62-6] are often used in combination with styrene to modify refractive index and improve uv resistance. Vinyltoluene [25013-15-4] and diaHyl phthalate [131-17-9] are employed as monomers in selective mol ding compositions for thermal improvements. [Pg.314]

Light-focusing plastic rods and other optical devices with graduated refractive indexes may use DADC and other monomers (29). Preparation and properties of plastic lenses from CR-39 are reviewed in reference 30. [Pg.83]

Properties and Applieations. Aryloxyphosphazene elastomers using phenoxy and J-ethylphenoxy substituents have found interest in a number of appHcations involving fire safety. This elastomer has a limiting oxygen index of 28 and contains essentially no halogens. It may be cured using either peroxide or sulfur. Peroxide cures do not require the allyhc cute monomer. Gum physical properties are as follows (17) ... [Pg.528]

Purified monomer is usually inhibited before shipment by such materials as copper resinate, diphenylamine or hydroquinone, which are generally removed before polymerisation. The monomer is a sweet-smelling liquid partially miscible with water and with the following properties boiling point at 760mmHg, 72.5°C specific gravity at 20°C, 0.934 refractive index 1.395 vapour... [Pg.387]

A more difficult criterion to meet with flow markers is that the polymer samples not contain interferents that coelute with or very near the flow marker and either affect its retention time or the ability of the analyst to reproducibly identify the retention time of the peak. Water is a ubiquitous problem in nonaqueous GPC and, when using a refractive index detector, it can cause a variable magnitude, negative area peak that may coelute with certain choices of totally permeated flow markers. This variable area negative peak may alter the apparent position of the flow marker when the flow rate has actually been invariant, thereby causing the user to falsely adjust data to compensate for the flow error. Similar problems can occur with the elution of positive peaks that are not exactly identical in elution to the totally permeated flow marker. Species that often contribute to these problems are residual monomer, reactants, surfactants, by-products, or buffers from the synthesis of the polymer. [Pg.549]

This technology has been utilized by BP Chemicals for the production of lubricating oils with well defined characteristics (for example, pour point and viscosity index). It is used in conjunction with a mixture of olefins (i.e., different isomers and different chain length olefins) to produce lubricating oils of higher viscosity than obtainable by conventional catalysis [33]. Unichema Chemie BV have applied these principals to more complex monomers, using them with unsaturated fatty acids to create a mixture of products [34]. [Pg.323]

Assuming that no intramolecular or side reactions take place and that all groups are equireactive, the polydispersity index, 7P, of hyperbranched polymers obtained by step-growth polymerization of ABX monomers is given by Eq. (2.2), where pA is die conversion in A groups.196 Note that the classical Flory relationship DPn = 1/(1 — pa) holds for ABX monomer polymerizations ... [Pg.57]

The refractive index detector, in general, is a choice of last resort and is used for those applications where, for one reason or another, all other detectors are inappropriate or impractical. However, the detector has one particular area of application for which it is unique and that is in the separation and analysis of polymers. In general, for those polymers that contain more than six monomer units, the refractive index is directly proportional to the concentration of the polymer and is practically independent of the molecular weight. Thus, a quantitative analysis of a polymer mixture can be obtained by the simple normalization of the peak areas in the chromatogram, there being no need for the use of individual response factors. Some typical specifications for the refractive index detector are as follows ... [Pg.185]

The normalization method is the easiest and most straightforward to use but, unfortunately, it is also the least likely to be appropriate for most LC analyses. To be applicable, the detector must have the same response to all the components of the sample. An exceptional example, where the normalization procedure is frequently used, is in the analysis of polymers by exclusion chromatography using the refractive index detector. The refractive index of a specific polymer is a constant for all polymers of that type having more than 6 monomer units. Under these conditions normalization is the obvious quantitative method to use. [Pg.271]

The micro-mixed reactor with dead-polymer model was developed to account for the large values of the polydispersity index observed experimentally. The effect of increasing the fraction of dead-polymer in the reactor feed while maintaining the same monomer conversion is to broaden the product polymer distribution and therefore to increase the polydispersity index. As illustrated in Table V, this model, with its adjustable parameter, can exactly match experiment average molecular weights and easily account for values of the polydispersity index significantly greater than 2. [Pg.322]

The effect of dead-polymer and by-passing on the micro-mixed reactor for the same degree of monomer conversion is to broaden the product polymer distribution and thus allow values of the polydispersity index much larger than 2. [Pg.323]

The general equation for the gel effect index, equation (la) which incorporates chain transfer, was used in those cases where there was not a good agreement between model predictions and experimental data. The same values of and (derived from the values of and C2 found at high rates) were used in the integration of equation (1) and the value of the constant of chain transfer to monomer, C, was taken as an adjustable parameter and used to minimize tfie error of fitting the time-conversion data by the model. [Pg.370]


See other pages where Monomers INDEX is mentioned: [Pg.59]    [Pg.118]    [Pg.254]    [Pg.59]    [Pg.118]    [Pg.254]    [Pg.2189]    [Pg.365]    [Pg.134]    [Pg.176]    [Pg.191]    [Pg.160]    [Pg.125]    [Pg.469]    [Pg.268]    [Pg.270]    [Pg.407]    [Pg.437]    [Pg.83]    [Pg.210]    [Pg.434]    [Pg.847]    [Pg.1110]    [Pg.483]    [Pg.331]    [Pg.279]    [Pg.32]    [Pg.303]   
See also in sourсe #XX -- [ Pg.347 ]




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