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Weight material

Separation of low-molecular-weight materials. Low-molecular-weight materials are distilled at high pressure to increase their condensing temperature and to allow, if possible, the use of cooling water or air cooling in the column condenser. Very low... [Pg.74]

Separation of high-molecular-weight heat-sensitive materials. High-molecular-weight materials are often heat sensitive and as such are usually distilled under vacuum to reduce their boiling temperature. [Pg.75]

In summary, distillation is not well suited for separating either low-molecular-weight materials or high-molecular-weight heat-sensitive materials. However, distillation might still be the best method for these cases, since the basic advantages of distillation... [Pg.75]

The most common alternative to distillation for the separation of low-molecular-weight materials is absorption. In absorption, a gas mixture is contacted with a liquid solvent which preferentially dissolves one or more components of the gas. Absorption processes often require an extraneous material to be introduced into the process to act as liquid solvent. If it is possible to use the materials already in the process, this should be done in preference to introducing an extraneous material for reasons already discussed. Liquid flow rate, temperature, and pressure are important variables to be set. [Pg.83]

The most common alternative to distillation for the separation of low-molecular-weight materials is absorption. Liquid flow rate, temperature, and pressure are important variables to be set, but no attempts should be made to carry out any optimization at this stage. [Pg.92]

The successful preparation of polymers is achieved only if tire macromolecules are stable. Polymers are often prepared in solution where entropy destabilizes large molecular assemblies. Therefore, monomers have to be strongly bonded togetlier. These links are best realized by covalent bonds. Moreover, reaction kinetics favourable to polymeric materials must be fast, so tliat high-molecular-weight materials can be produced in a reasonable time. The polymerization reaction must also be fast compared to side reactions tliat often hinder or preclude tire fonnation of the desired product. [Pg.2515]

Some 2,000—3,000 t/yr of these specialty alcohols are produced ia the United States (Exxon) and ia Germany (Henkel) (28). Their high Hquidity because of branching permits use of less volatile, higher molecular weight materials, reported to be less irritating than the lower molecular weight linear alcohol materials, ia a variety of cosmetic products (29). [Pg.460]

Polyesters were initially discovered and evaluated ia 1929 by W. H. Carothers, who used linear aliphatic polyester materials to develop the fundamental understanding of condensation polymerisation, study the reaction kinetics, and demonstrate that high molecular weight materials were obtainable and could be melt-spun iato fibers (1 5). [Pg.325]

Many perfluoroaUphatic ethers and tertiary amines have been prepared by electrochemical fluorination (1 6), direct fluorination using elemental fluorine (7—9), or, in a few cases, by fluorination using cobalt trifluoride (10). Examples of lower molecular weight materials are shown in Table 1. In addition to these, there are three commercial classes of perfluoropolyethers prepared by anionic polymerization of hexafluoropropene oxide [428-59-1] (11,12), photooxidation of hexafluoropropene [116-15-4] or tetrafluoroethene [116-14-3] (13,14), or by anionic ring-opening polymeriza tion of tetrafluorooxetane [765-63-9] followed by direct fluorination (15). [Pg.296]

Dowtherm G is a mixture of di- and triaryl compounds and has good flow characteristics at low temperatures. Dowtherm G is highly stable, and the products of decomposition consist of high molecular weight materials which remain in solution in the Hquid. Dowtherm G is intended for use in Hquid-phase systems. The fluid has a striking odor even at extremely low concentrations. [Pg.504]

Mixtures. A number of mixtures of the hehum-group elements have been studied and their physical properties are found to show Httle deviation from ideal solution models. Data for mixtures of the hehum-group elements with each other and with other low molecular weight materials are available (68). A similar collection of gas—soHd data is also available (69). [Pg.9]

The low molecular weight materials produced by this process are used as lubricants, whereas the high molecular weight materials, the polyisobutylenes, are used as VI improvers and thickeners. Polybutenes that are used as lubricating oils have viscosity indexes of 70—110, fair lubricating properties, and can be manufactured to have excellent dielectric properties. Above their decomposition temperature (ca 288°C) the products decompose completely to gaseous materials. [Pg.264]

Electrochemical Synthesis. Electrochemical methods have also been investigated for the synthesis of polysilanes, but these have so far yielded low molecular weight materials (113,114). [Pg.262]

Barite, predominately BaSO, meets the overall requirements for weighting material better than other materials and is used for increasing the density of drilling fluids throughout the world. Commercial barite has a lower specific gravity than pure barium sulfate owing to the presence of associated minerals, such as silica. Barite is virtually insoluble in water and does not react with other mud constituents. Most operators prefer barite that meets API specifications (Table 2) (23). The barite content in mud depends on the desired density but can be as high as 2000 kg/km (700 lb/bbl). [Pg.176]

Glass-Transition Temperatures. The glass-transition temperature, T, of fully hydrolyzed PVA has been determined to be 85°C for high molecular weight material. The glass transition in case of 87—89% hydrolyzed PVA varies according to the following formula (59) ... [Pg.476]

Fluid or Pour-Tjpe Resins. Fluid or pour-type resins are modified acryHc systems that can be cured chemically. A fine-particle-size polymer powder consisting mostly of high molecular weight material is preferred to prevent a rapid increase in viscosity during mixing and pouring. Polymerization occurs in flexible... [Pg.488]


See other pages where Weight material is mentioned: [Pg.75]    [Pg.77]    [Pg.558]    [Pg.266]    [Pg.66]    [Pg.274]    [Pg.233]    [Pg.299]    [Pg.355]    [Pg.14]    [Pg.258]    [Pg.264]    [Pg.265]    [Pg.262]    [Pg.255]    [Pg.162]    [Pg.176]    [Pg.177]    [Pg.178]    [Pg.179]    [Pg.274]    [Pg.279]    [Pg.360]    [Pg.429]    [Pg.535]    [Pg.171]    [Pg.166]    [Pg.62]    [Pg.368]    [Pg.495]    [Pg.531]    [Pg.144]    [Pg.156]    [Pg.475]   
See also in sourсe #XX -- [ Pg.571 ]




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Active materials weights

High-molecular-weight DNA materials

Higher molecular weight organic materials

Low molecular weight organic materials

Low-molecular-weight oxidized materials

Low-molecular-weight oxidized materials LMWOM)

Material Densities and. Atomic Weights

Molecular weight of the starting material

Molecular weight polyimide materials

Starting material, molecular weight

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