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Polymer systems, controlled, listed

The equipment for yam extrusion and their fimc-tions are listed in Table 8.42. Independently controlled heaters heated the extmder barrel and the connecting flange with the gear pump, casing of the pump, and the extmsion die. Temperatures of the heaters were set to allow the melt to reach a specified temperature. The gear pump was set to control the melt flow rate to maintain a constant feed to the die. The cooling system consisted of laminar airflow, radially directed from the inside towards the outside at an air speed of 3 m/sec. The air duct was positioned at a distance of about 1 cm from the filament outlet. Process conditions and yam properties for various polymers have been listed in Tables 8.43 and 8.44. [Pg.240]

Telechelic polymers rank among the oldest designed precursors. The position of reactive groups at the ends of a sequence of repeating units makes it possible to incorporate various chemical structures into the network (polyether, polyester, polyamide, aliphatic, cycloaliphatic or aromatic hydrocarbon, etc.). The cross-linking density can be controlled by the length of precursor chain and functionality of the crosslinker, by molar ratio of functional groups, or by addition of a monofunctional component. Formation of elastically inactive loops is usually weak. Typical polyurethane systems composed of a macromolecular triol and a diisocyanate are statistically simple and when different theories listed above are... [Pg.131]

Membranes with extremely small pores ( < 2.5 nm diameter) can be made by pyrolysis of polymeric precursors or by modification methods listed above. Molecular sieve carbon or silica membranes with pore diameters of 1 nm have been made by controlled pyrolysis of certain thermoset polymers (e.g. Koresh, Jacob and Soffer 1983) or silicone rubbers (Lee and Khang 1986), respectively. There is, however, very little information in the published literature. Molecular sieve dimensions can also be obtained by modifying the pore system of an already formed membrane structure. It has been claimed that zeolitic membranes can be prepared by reaction of alumina membranes with silica and alkali followed by hydrothermal treatment (Suzuki 1987). Very small pores are also obtained by hydrolysis of organometallic silicium compounds in alumina membranes followed by heat treatment (Uhlhom, Keizer and Burggraaf 1989). Finally, oxides or metals can be precipitated or adsorbed from solutions or by gas phase deposition within the pores of an already formed membrane to modify the chemical nature of the membrane or to decrease the effective pore size. In the last case a high concentration of the precipitated material in the pore system is necessary. The above-mentioned methods have been reported very recently (1987-1989) and the results are not yet substantiated very well. [Pg.18]

Much of the work related to environmental and medical devices required hydro-philicity. This property is inexorably bound to the swelling of the polymer in water. The amount of swell or hydrophilicity is controlled by the polyol used to build the polyurethane. In many cases, the design of the system requires a compromise of hydrophilicity and physical strength, and the choice of polyol is the chief tool. We stated earlier that block copolymers were suitable for intermediate levels of hydrophilicity. Table 3.5 lists a series of polymers and their equilibrium values. Each polymer is the result of proper selection of an EO or PO copolymer. The table can be used as a guide in designing polymers of intermediate hydrophilicity. [Pg.74]

An analysis of the ionic factors for the polymerization of dienes to cis and trans structures is possible in the same way as for isotactic mono-enes. The mechanism which controls the steric structure of poly 1,4 dienes is parallel to that we have already seen for the mono-olefins. Roha (2) listed the catalysts which polymerize dienes according to the polymer structures produced. It was shown that the highly anionic as well as the highly cationic catalyst systems with increasing ionic separation produced trans-poly-1,4-dienes. This is analogous to the production of syndiotactic polyolefins. [Pg.381]

Suspension Polymerization Systems for Controlling Particle Size. Suspending Agents. Both types of suspension stabilizers—the finely divided water-insoluble solids and the soluble film formers—have been used extensively to prepare styrene polymers of a particle size between about 10 and 40 mesh. Examples of such materials are listed below ... [Pg.535]

The example is taken from a polymerization batch process and has also been referred to previously by Dahl et al. [1999] and Kosanovich et al. [1996], The dataset consists of 50 batches from which eight process variables are measured over approximately 120 time intervals. From this set of batches, two quality variables on the final product were also available. Both process and quality variables are listed in Table 10.7. The reactor in this chemical process (see Figure 10.26) converts the aqueous effluent from an upstream evaporator into a polymer product. The reactor consists of an autoclave and a cooling/heating system. It also has a vent to control the vapor pressure in the autoclave. The recipe specifies reactor and heat source pressure trajectories through five stages. [Pg.291]

With this much interest in polyethylene, many attempts have been made to use low frequency NMR in either the time domain or frequency domain to monitor and control the production more rapidly. Auburn International (now part of Oxford Instruments) developed a widely adopted system based on the time domain spectrometers [21]. In this case, sample preparation is no longer an issue since the system accepts either powder or pellets and no solvent is used. The Auburn systems determine crystalline and amorphous ratios, viscosity, melt index and molecular weight For other types of polymers, the list of advertised measurements include tacticity, rubber content, copolymer analysis, and various rheological properties. These values are determined by correlating several routine but laborious methods with the decay of the NMR signal under various pulse sequences. The man-hours... [Pg.901]


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Polymer listed

Polymers listing

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