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Acrylamide polyacrylamides

Focused proteins are separated according to their molecular weight in 12.5% acrylamide and 2.6% bis-acrylamide polyacrylamide gels using the Tris-glycine system (see Note 8). [Pg.37]

POWDERS,HANDLING - DISPERSION OF POWDERS IN LIQUIDS] (Vol 19) -polyacrylamides in [ACRYLAMIDE POLYMERS] (Voll)... [Pg.76]

Hydrolyzed Polyacrylamide. HPAM (6) can be prepared by a free-radical process ia which acrylamide is copolymerized with incremental amounts of acryUc acid or through homopolymerization of acrylamide followed by hydrolysis of some of the amide groups to carboxylate units. [Pg.317]

In this article the term acrylamide polymer refers to all polymers which contain acrylamide as a major constituent. Consequendy, acrylamide polymers include functionalized polymers prepared from polyacrylamide by postreaction and copolymers prepared by polymerizing acrylamide (2-propenamide, C H NO) with one or more comonomers. [Pg.139]

Hydrolysis of cationic polyacrylamides prepared from copolymeri2ation of acrylamide and cationic ester monomer can occur under very mild conditions. A substantial loss in cationicity can cause a significant loss in performance in many apphcations. Copolymers [69418-26-4] of acrylamide and acryloxyethyltrimethylammonium chloride [44992-01 -0] CgH gN02(Cl), for instance, lose cationicity rapidly at alkaline pH (37). [Pg.140]

Methylol Formation. Polyacrylamide reacts with formaldehyde to form an /V-methylo1 derivative. The reaction is conducted at pH 7—8.8 to avoid cross-linking, which will occur at lower pH. The copolymer can also be prepared by copolymerizing acrylamide with commercially available A/-methylolacrylamide [924-42-5] C4H2NO2. These derivatives are useful in several mining appHcations (49,50). They are also useful as chemical grouts. [Pg.141]

Polyacrylamides are manufactured by free-radical polymerization of acrylamide to form chains of the stmcture shown, where n can range from several up to 400,000. [Pg.141]

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]

Microemulsion Polymerization. Polyacrylamide microemulsions are low viscosity, non settling, clear, thermodynamically stable water-in-od emulsions with particle sizes less than about 100 nm (98—100). They were developed to try to overcome the inherent settling problems of the larger particle size, conventional inverse emulsion polyacrylamides. To achieve the smaller microemulsion particle size, increased surfactant levels are required, making this system more expensive than inverse emulsions. Acrylamide microemulsions form spontaneously when the correct combinations and types of oils, surfactants, and aqueous monomer solutions are combined. Consequendy, no homogenization is required. Polymerization of acrylamide microemulsions is conducted similarly to conventional acrylamide inverse emulsions. To date, polyacrylamide microemulsions have not been commercialized, although work has continued in an effort to exploit the unique features of this technology (100). [Pg.143]


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See also in sourсe #XX -- [ Pg.161 ]




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