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Polymerization equipments

In particular, if a latex is to be used for coatings, adhesives, or film applications, no silicone-base stopcock greases should be used on emulsion polymerization equipment. Although hydrocarbon greases are not completely satisfactory either, there are very few alternatives. Teflon tapes, sleeves, and stoppers may be useful, although expensive. [Pg.32]

A 50-ml glass ampoule used for polymerization equipped with a septum with a syringe needle for the inlet of nitrogen and extending below the surface of the reactants and another syringe needle to go above the reactants to act as an exit for the HC1 that is generated in this reaction... [Pg.59]

Add 6.3 g (0.0310 mol) of isophthaloyl chloride and 2.8 g (0.0311 mol) of 1,4-butanediol (1% excess) to a 50-ml ampule used for polymerization equipped with a capillary tube for a nitrogen inlet extending below the surface of the reaction mixture. [Pg.60]

UV polymerization equipment Multiray lamp M1-998 long-wave UV bulb 11-998-4 blk-ray UV meter 984-53]... [Pg.183]

Should branching become excessive, infinite networks can form. The products become crosslinked, insoluble, and infusible. Such materials are called popcorn polymers. This phenomenon is more common in bulk polymerizations. The crosslinked polymers form nodules that occupy much more volume than the monomers from which they formed and often clog up the polymerization equipment, sometimes even rupturing it. [Pg.238]

Over the last 35 years, the process for manufacturing PC has undergone significant modernization and evolution. Early process attempts at melt transesteriflcation and solution polymerization with pyridine were both deemphasized based on equipment limitations and economics, respectively. Both batch and continuous processes are practiced today. Solution polymerization in methylene chloride in contact with aqueous sodium hydroxide has become the preferred process by some major producers. Melt polymerization has also regained attention, facilitated by improvements in polymerization equipment. Melt polymerization also addresses recent concerns with potential release of volatile organic compounds into the environment. [Pg.596]

Thermally activated initiators such as azobisisobutyronitrile (AIBN), ammonium persulfate, or benzoyl peroxide can be used in solution polymerization, but these initiators are slow acting at temperatures required for fiber-grade polymer processes. Half-lives for this type of initiator are in the range of 10-20 h at 50-60° C (30). Therefore, these initiators are used mainly in batch processes where the reaction is carried out over an extended time. Redox initiators, such as the ammonium persulfate/sodium bisulfite/copper system, have much higher initiation rates and are reported to be employed in the Acordis NaSCN process. A typical continuous solution polymerization equipment diagram is shown in Figure 7. [Pg.188]

A wide variety of polystyrene-like polymers and copolymers (crystal. Impact modified, ABPMS, PMS-AN, PMS-BR, PMS-MA and PMS-MMA)(28) have been prepared from PMS using bulk, solvent and suspension polymerization techniques in our laboratories and pilot plants using thermal, anionic and chemical initiation. From a resin manufacturing point of view, PMS monomer can be processed in existing styrene polymerization equipment to produce poly-PMS analogues. However, process development must be done to optimize conditions for each resin type. [Pg.233]

The monomer must be charged to polymerization equipment in the hood. The discharging of materials also must take place in the hood. Excess monomer must be allowed to evaporate completely in the hood with the door closed. [Pg.355]


See other pages where Polymerization equipments is mentioned: [Pg.987]    [Pg.193]    [Pg.136]    [Pg.987]    [Pg.267]    [Pg.125]    [Pg.92]    [Pg.92]    [Pg.410]    [Pg.287]    [Pg.136]    [Pg.331]    [Pg.912]    [Pg.500]    [Pg.384]    [Pg.476]    [Pg.230]    [Pg.47]    [Pg.224]    [Pg.410]   
See also in sourсe #XX -- [ Pg.193 ]




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Emulsion polymerization equipment

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