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Cross molecular weight

Fig. 1. Permeability of Nitella cell membranes to non-electrolytes in relation to the olive oil solubility of these solutes. On the ordinate the logarithm of the permeability (in units of 10 cm/sec) on the abscissa, the logarithm of the olive oil/water partition coefficient of the permeant. Data measured at 20°C. Crosses molecular weight up to 50 open circles molecular weights from 60 to 119 filled circles molecular weights above 120. Data taken from Collander [3]. The straight line is of unit slope. Fig. 1. Permeability of Nitella cell membranes to non-electrolytes in relation to the olive oil solubility of these solutes. On the ordinate the logarithm of the permeability (in units of 10 cm/sec) on the abscissa, the logarithm of the olive oil/water partition coefficient of the permeant. Data measured at 20°C. Crosses molecular weight up to 50 open circles molecular weights from 60 to 119 filled circles molecular weights above 120. Data taken from Collander [3]. The straight line is of unit slope.
CO—C H,—CO—0—CHj—CHOH—CHj—OOC—CgH,—CO— These are comparatively soft materials and they are soluble in a number of organic solvents. Under more drastic conditions (200-220°) and with a larger proportion of phthahc anhydride, the secondary alcohol groups are esterified and the simple chains become cross-hnked three dimensional molecules of much higher molecular weight are formed ... [Pg.1018]

Epoxy novolac resins are produced by glycidation of the low-molecular-weight reaction products of phenol (or cresol) with formaldehyde. Highly cross-linked systems are formed that have superior performance at elevated temperatures. [Pg.1015]

A cross-linked polymer has a density of 0.94 g cm" at 25°C and a molecular weight between crosslinks of 28,000. The conformation of one bond in the middle of the molecule changes from trans to gauche, and the molecule opens up by 120°. In w-butane, the trans to gauche transformation requires about 3.3 kJ mol". Estimate a value for AH of stretching based on this model, and use the law of cosines to estimate the magnitude of the opening up that results. [Pg.142]

Suppose the un-cross-linked polymer chain has a molecular weight M which, upon crosslinking, is divided into subchains of molecular weight M, . This means that each subchain is a fraction of the original chain. Since the crosslink... [Pg.151]

The four regions of behavior shown by the polymers in Fig. 3.9 are fairly typical of high molecular weight un-cross-linked polymers. Let us examine the four regions of behavior, this time in terms of what is happening at the molecular level ... [Pg.164]

An important application of Eq. (3.39) is the evaluation of M, . Flory et al.t measured the tensile force required for 100% elongation of synthetic rubber with variable crosslinking at 25°C. The molecular weight of the un-cross-linked polymer was 225,000, its density was 0.92 g cm , and the average molecular weight of a repeat unit was 68. Use Eq. (3.39) to estimate M. for each of the following samples and compare the calculated value with that obtained from the known fraction of repeat units cross-linked ... [Pg.194]

In some cases of multifunctional monomers the possibility exists for branches on branches, which ultimately result in cross-linked products and effectively infinite molecular weights well before p reaches unity. [Pg.299]

It has been hypothesized that cross-linked polymers would have better mechanical properties if interchain bridges were located at the ends rather than the center of chains. To test this, low molecular weight polyesters were synthesizedf... [Pg.302]

An example of a size-exclusion chromatogram is given in Figure 7 for both a bench-scale (23.5 mL column) separation and a large-scale (86,000 mL column) mn. The stationary phase is Sepharose CL-6B, a cross-linked agarose with a nominal molecular weight range of 5000-2 x 10 (see Fig. 6) (31). [Pg.49]

Furfural reacts with ketones to form strong, crosslinked resins of technical interest in the former Soviet Union the U.S. Air Force has also shown some interest (42,43). The so-called furfurylidene acetone monomer, a mixture of 2-furfurylidene methyl ketone [623-15-4] (1 )> bis-(2-furfurylidene) ketone [886-77-1] (14), mesityl oxide, and other oligomers, is obtained by condensation of furfural and acetone under basic conditions (44,45). Treatment of the "monomer" with an acidic catalyst leads initially to polymer of low molecular weight and ultimately to cross-linked, black, insoluble, heat-resistant resin (46). [Pg.79]

When -xylene is used as the monomer feed in a plasma polymer process, PX may play an important role in the formation of the plasma polymer. The plasma polymer from -xylene closely resembles the Gorham process polymer in the infrared, although its spectmm contains evidence for minor amounts of nonlinear, branched, and cross-linked chains as well. Furthermore, its solubiUty and low softening temperature suggest a material of very low molecular weight (15). [Pg.430]

Solution polyacrylamides can also be prepared at high polymer soHds by radiation processes (80,81). Polyacrylamides with molecular weights up to 20 million can be prepared by inradiation of acrylamide and comonomers in a polyethylene bag with cobalt-60 gamma radiation at dose rates of 120-200 J/kg-h. The total dose of radiation is controlled to avoid cross-linking. [Pg.142]

The polymeric products can be made to vary widely in physical properties through controlled variation in the ratios of monomers employed in thek preparation, cross-linking, and control of molecular weight. They share common quaHties of high resistance to chemical and environmental attack, excellent clarity, and attractive strength properties (see Acrylic ester polymers). In addition to acryHc acid itself, methyl, ethyl, butyl, isobutyl, and 2-ethylhexyl acrylates are manufactured on a large scale and are available in better than 98—99% purity (4). They usually contain 10—200 ppm of hydroquinone monomethyl ether as polymerization inhibitor. [Pg.148]

The isocyanates used with rigid foam systems are either polymeric MDI or specialty types of TDI. Both contain various levels of polymerized isocyanate groups which contribute to molecular weight per cross-link and also may affect reactivity due to steric hindrance of some isocyanate positions. [Pg.418]

The physical properties of any polyisoprene depend not only on the microstmctural features but also on macro features such as molecular weight, crystallinity, linearity or branching of the polymer chains, and degree of cross-linking. For a polymer to be capable of crystallization, it must have long sequences where the stmcture is completely stereoregular. These stereoregular sequences must be linear stmctures composed exclusively of 1,4-, 1,2-, or 3,4-isoprene units. If the units are 1,4- then they must be either all cis or all trans. If 1,2- or 3,4- units are involved, they must be either syndiotactic or isotactic. In all cases, the monomer units must be linked in the head-to-tail manner (85). [Pg.467]


See other pages where Cross molecular weight is mentioned: [Pg.188]    [Pg.193]    [Pg.2526]    [Pg.2603]    [Pg.2818]    [Pg.189]    [Pg.41]    [Pg.67]    [Pg.162]    [Pg.268]    [Pg.527]    [Pg.50]    [Pg.52]    [Pg.53]    [Pg.121]    [Pg.315]    [Pg.140]    [Pg.141]    [Pg.141]    [Pg.233]    [Pg.233]    [Pg.312]    [Pg.307]    [Pg.325]    [Pg.352]    [Pg.387]    [Pg.406]    [Pg.530]    [Pg.330]    [Pg.435]    [Pg.448]    [Pg.70]    [Pg.375]    [Pg.451]    [Pg.459]   
See also in sourсe #XX -- [ Pg.276 ]




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Cross-link number average molecular weight

Cross-linking, and molecular weight

Cross-links molecular weight

Molecular weight between cross-links

Molecular weight per cross-link

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