Polymers polyamines

Polyamine/DADMAC polymers Polyamine/EPIDMA polymers Polyamines... 

COLIPOSITEIvL TERLALS - POLYMER-MATRIX - THERMOSETS] (Vol 7) Glycidated polyamine (N,NHyHy-tetragl ycidyl-4,4y-diaminodiphenylmethane [28768-32-3]... 

Synthetic Polymers. Examples of polymers in this class include acrylamide—acryHc polymers and their derivatives, polyamines and their derivatives, poly-(ethylene oxide), and allylamine polymers. 

PoIya.mines are condensation polymers containing nitrogen they are made by a variety of synthetic routes. Most of the commercial polyamines are made by reaction of epichlorohydrin with amines such as methylamine [25988-97-0] or dimethylamine [39660-17-8] (18,19). Branching can be increased by a dding small amounts of diamines such as ethylenediamine [42751-79-1]. A typical stmcture of this type of polyamine is stmcture (9). 

Polyamines can also be made by reaction of ethylene dichloride with amines (18). Products of this type are sometimes formed as by-products in the manufacture of amines. A third type of polyamine is polyethyleneimine [9002-98-6] which can be made by several routes the most frequently used method is the polymeriza tion of azitidine [151 -56 ] (18,26). The process can be adjusted to vary the amount of branching (see Imines, cyclic). Polyamines are considerably lower in molecular weight compared to acrylamide polymers, and therefore their solution viscosities are much lower. They are sold commercially as viscous solutions containing 1—20% polymer, and also any by-product salts from the polymerization reaction. The charge on polyamines depends on the pH of the medium. They can be quaternized to make their charge independent of pH (18). 

The polymer market ia the United States is dominated by synthetics with natural polymers constituting about one-eighth ia monetary terms (88). Of the synthetic polymers, most are based on acrylamide. A Hst of producers is as follows producers ia the left-hand column also produce polyamines and p oly qu atemarie s. 

Addition Polymers. The most commonly referenced reaction of isocyanates iavolves their addition to polyhydroxyl, polyamine, or polycarboxyhc acid compounds to yield addition polymers. Due to the wide diversity of raw material characteristics and the broad range of functionahty, polyurethane polymers having a wide range of processiag and performance characteristics are available. 

Formaldehyde may react with the active hydrogens on both the urea and amine groups and therefore the polymer is probably highly branched. The amount of formaldehyde (2—4 mol per 1 mol urea), the amount and kind of polyamine (10—15%), and resin concentration are variable and hundreds of patents have been issued throughout the world. Generally, the urea, formaldehyde, polyamine, and water react at 80—100°C. The reaction may be carried out in two steps with an initial methylolation at alkaline pH, followed by condensation to the desired degree at acidic pH, or the entire reaction may be carried out under acidic conditions (63). The product is generally a symp with 25—35% soHds and is stable for up to three months. 

Isocyanates. The commodity isocyanates TDI and PMDI ate most widely used in the manufacture of urethane polymers (see also Isocyanates, organic). The former is an 80 20 mixture of 2,4- and 2,6-isomers, respectively the latter a polymeric isocyanate obtained by phosgenation of aniline—formaldehyde-derived polyamines. A coproduct in the manufacture of PMDI is 4,4 -methylenebis(phenyHsocyanate) (MDI). A 65 35 mixture of 2,4- and 2,6-TDI, pure 2,4-TDI and MDI enriched in the 2,4 -isomer are also available. The manufacture of TDI involves the dinitration of toluene, catalytic hydrogenation to the diamines, and phosgenation. Separation of the undesired 2,3-isomer is necessary because its presence interferes with polymerization (13). 

Some commercial durable antistatic finishes have been Hsted in Table 3 (98). Early patents suggest that amino resins (qv) can impart both antisHp and antistatic properties to nylon, acryUc, and polyester fabrics. CycHc polyurethanes, water-soluble amine salts cross-linked with styrene, and water-soluble amine salts of sulfonated polystyrene have been claimed to confer durable antistatic protection. Later patents included dibydroxyethyl sulfone [2580-77-0] hydroxyalkylated cellulose or starch, poly(vinyl alcohol) [9002-86-2] cross-linked with dimethylolethylene urea, chlorotria2ine derivatives, and epoxy-based products. Other patents claim the use of various acryUc polymers and copolymers. Essentially, durable antistats are polyelectrolytes, and the majority of usehil products involve variations of cross-linked polyamines containing polyethoxy segments (92,99—101). 

Additives for lubricating oils providing a combination of viscosity index improvement (VII) and dispersancy have also been reported. These additives are prepared from ethyleneamines by reaction with various Vll-type polymers that have been chlorinated or modified in some other way to provide an ethyleneamine reaction site. Antimst additives for lubricating oils have been prepared by reaction of polyamines with fatty acids followed by reaction with polyalkylenesuccinic anhydrides (178,179). 

In presence of polyamines the maximum of light absorption of indicated triphenylmethane dyes displaces on 10-30 nm, for azo dyes the shift of the band reaches 50-80 nm. The greatest difference of light absorption of associates and reagents is watched for BKM at pH 5,05, for BPR at pH 4,20, for CPR in an interval pH 5,05-5,45. At these pH dyes are anions, it promotes interaction with a cationic surface-active substance. The ratios between polymer and BKM, BPR, CPR are established by spectroscopy method, its equal 1 20, 1 20 and 1 30 accordingly. 

Last years the polymeric surface - active substances began to use as modifiers of organic reagent properties. In our work the behavior of synthetic polymers (polysulphonilpiperidinilmethylenhydroxide (PSPMH), polyvinylpyrrolidone (PVP), polyamines - polyguanidine and metacide) and natural polymers (starch, gelatin) for various molecular masses are investigated. 

In the absence of ammonia and the concentration of polyamines being > 20 p.M the production of sediments take place. Ethylene diamine reacts with Hg(II) in the form of diimide -HNRNH- to form the insoluble complex IHgHNRNHHgl. In the presence of ammonia the production of sediments having complex composition is also possible. Given concentration of K Hgl 1-2 mM, NaOH 60-120 mM and compai able amounts of ammonia and ethylene diamine the products of reactions ai e only the soluble green-coloured complexes, bearing ammonia in the form of nitride and ethylene diamine in the form of diimide. Those complexes ai e polymers, with their absorption spectmms being different from those of the similar polymeric ammonia complexes. 

The use of bonded, silica column supports has also become a useful way to characterize cationic, water-soluble polymers. CATSEC SEC columns from Micra Scientific contain a silica support with a polymerized polyamine-bonded phase. This imparts a cationic surface charge on the packing that can be... 

The majority of hydrophilic and water-soluble polymers are manufactured on the commercial level. Their list includes PAAm, copolymers of AAm, PAAc, PEO, PVA, poly(jY-vinylpyrrolidone), some polyamines etc. So, it seems practically highly attractive to produce hydrogels based on these polymers using various crosslinking techniques. 

Crosslinking using reactions of multifunctional reagents with side groups of polymers is most frequently applied to PVA, some biopolymers containing OH-groups, partly hydrolyzed PAAm, polyamines, and other polymers. These reactions are reviewed in Ref. [52],... 

Hyperbranched aromatic polyesters, synthesis of, 116-118 Hyperbranched aromatic polymers, 286 Hyperbranched polyamine, synthesis of, 519-520... 

A matching search was made of the data available for two highly polar classes of chemicals — polyamines and polyalcohols — to find the polymer likely to be most resistant to chemical permeation by such highly polar compounds. 

Table II. Polyamines and Polyalcohols Matched by Material (Polymer)...

Only three of the polymers tested were resistant to both polyamines and polyolalcohols for at least one hour. 

The final resin product is obtained by reacting (curing or crosslinking) the above di-epoxide with acid anhydrides or polyamines. The curing agents (sometimes incorrectly called catalysts) react with the three-membered epoxide rings to produce a highly crosslinked polymer. 

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