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High-Molecular Components

There is evidence that gyrometrin does not exist in the free state in the mushroom, but rather is bound to an unknown high-molecular component. Therefore, fruiting bodies have to be heated with water in a closed tube at 120°C for several hours before methylhydrazine can be extracted with chloroform under an atmosphere of nitrogen. Gas chromotography and TLC have been used for its identification. [Pg.80]

The data on kp and kt as reported in the literature differ considerably. Therefore, we conducted new studies on methyl methacrylate (MMA), benzyl methacrylate (BMA), and styrene (St) as monomers. The constants were obtained by applying the method of intermittent illumination (rotating sector) combined with stationary state methods. The viscosity of the solvents varied between 0.5 and 100 cP. No mixed solvents composed of low- and high-molecular components were used but pure solvents only, the molecules of which did not deviate very much from a spherical form (methyl formate, diethyl phthalate, diethyl malonate, dimethyl glycol phthalate, etc.). [Pg.14]

Various average quantities are related as F Pw Pz Pz + y The equality sign is only valid for strictly monodisperse polymers. The number average values F or M are very sensitive to the presence of low molecular components, even when these are present in very small amounts. The higher averages, Fz or Mz, are strongly affected by the presence of high molecular components, even in trace concentrations. [Pg.530]

Fig. 36. Craze fibril stability — 8, in the PS blends (2,000 + 1,800,000) for ultraclean specimens (strain rate = 3x10 s ) as a function of %, the weight fraction of the high molecular component in the blend The solid curve is a prediction from the model of fibril breakdown, Eq. (41)... Fig. 36. Craze fibril stability — 8, in the PS blends (2,000 + 1,800,000) for ultraclean specimens (strain rate = 3x10 s ) as a function of %, the weight fraction of the high molecular component in the blend The solid curve is a prediction from the model of fibril breakdown, Eq. (41)...
Soluble polyvinylpyrrolidone was first used during World War II as a blood-plasma substitute. Although it has excellent properties for this purpose, it has no longer been used for a number of decades. The organism does not metabolize the polymer, with the result that after parenteral administration, small quantities of high-molecular components may remain within the body. This problem does not exist with oral administration. [Pg.3]

Table 19. Limits for the low and high-molecular components of povidone according to Jap.Ph.XII (former monographs)... Table 19. Limits for the low and high-molecular components of povidone according to Jap.Ph.XII (former monographs)...
High molecular components may be found in the effluent of some reactors, as for cracking, oxidation, etc. Because there is a danger of fouling downstream units, these heavies should be removed before other separators. Fig. 7.22 presents some solutions. An adsorption device, as for example a clay tower, could solve partially the problem. [Pg.272]

Under these conditions the reactions leading to increase of the molecular mass do not exhibit any essential influence. This is also confirmed by the profiles of the molecular mass distribution (MMD) of low and high molecular components (Fig. 39). [Pg.452]

Ultrafiltration is used over a wide field of applications involving situations where high molecular components have to be separated from low molecular components. Applications... [Pg.295]

The presence of proteins, polymers and other substances with high molecular weights sometimes affects the polarographic waves of the substance to be analysed. These effects are often caused by the formation of an adsorbed layer at the dropping mercury electrode. Thus it is sometimes preferable to separate first the high-molecular components before the solution is polarographed. [Pg.176]

A major problem whidi has to be fac in all repetitive-type syntheses where excess reagents are used is the purification of the polymer or the removal of low-molecular compounds. Be e prediction of the sui rt, lich apfdied even in the beginning of the use of soluble polymers before being refined later by the introduction of crystalline polymers, in many studies on liquid-phase application, membrane filtration was also used for the separation of low- and high-molecular components in solution [10, 25-28,42-48]. The experimental arrangement of a typncal membrane filtration system is depicted in Fig. 1. [Pg.38]

You can add restraints to any molecular mechanics calculation (single point, optimization or dynamics). These might be NMR restraints, for example, or any situation where a length, angle, or torsion is known or pre-defined. Restraints with large force constants result in high frequency components in a molecular dynamics calculation and can result in instability under some circumstances. [Pg.203]

For mixture.s the picture is different. Unless the mixture is to be examined by MS/MS methods, usually it will be necessary to separate it into its individual components. This separation is most often done by gas or liquid chromatography. In the latter, small quantities of emerging mixture components dissolved in elution solvent would be laborious to deal with if each component had to be first isolated by evaporation of solvent before its introduction into the mass spectrometer. In such circumstances, the direct introduction, removal of solvent, and ionization provided by electrospray is a boon and puts LC/MS on a level with GC/MS for mixture analysis. Further, GC is normally concerned with volatile, relatively low-molecular-weight compounds and is of little or no use for the many polar, water soluble, high-molecular-mass substances such as the peptides, proteins, carbohydrates, nucleotides, and similar substances found in biological systems. LC/MS with an electrospray interface is frequently used in biochemical research and medical analysis. [Pg.59]

High molecular weight components, which can be important in extmsion processes, can be accurately measured in steady shear experiments (34). [Pg.408]

Equatioa-of-state theories employ characteristic volume, temperature, and pressure parameters that must be derived from volumetric data for the pure components. Owiag to the availabiHty of commercial iastmments for such measurements, there is a growing data source for use ia these theories (9,11,20). Like the simpler Flory-Huggias theory, these theories coataia an iateraction parameter that is the principal factor ia determining phase behavior ia bleads of high molecular weight polymers. [Pg.409]

Use of 1,3 cycloaHphatic diamines in polyamides may be similarly limited by internal amide dehydration of the conformationaHy labile cis isomers to form a tetrahydropyrimidine (38) rather than high molecular weight polyamide. 1,3-Cyclohexanediamine is, however, a component of Spandex polyureas Du Pont uses the hydrogenation product of y -phenylenediamine [108-45-2] (24) captively to produce Lycra (see Fibers, elastomeric). [Pg.213]

Because plastics are almost invariably modified with one or more additives, there are three components of chemical analysis the high molecular weight portion, ie, the polymer the additives, ie, plasticizer and mold-release agent and the residuals remaining from the polymerization process. The high... [Pg.525]


See other pages where High-Molecular Components is mentioned: [Pg.13]    [Pg.86]    [Pg.409]    [Pg.532]    [Pg.530]    [Pg.13]    [Pg.86]    [Pg.549]    [Pg.518]    [Pg.154]    [Pg.640]    [Pg.1606]    [Pg.13]    [Pg.86]    [Pg.409]    [Pg.532]    [Pg.530]    [Pg.13]    [Pg.86]    [Pg.549]    [Pg.518]    [Pg.154]    [Pg.640]    [Pg.1606]    [Pg.346]    [Pg.371]    [Pg.140]    [Pg.50]    [Pg.121]    [Pg.57]    [Pg.121]    [Pg.193]    [Pg.32]    [Pg.71]    [Pg.397]    [Pg.430]    [Pg.270]    [Pg.233]    [Pg.321]    [Pg.409]    [Pg.27]    [Pg.344]    [Pg.536]   


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High components

High-Molecular Components Separation

High-molecular-weight components

Molecular components

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