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POLYETHER DIAMINE

Copolymers of methacrylic add and ethylene termed as ethylene ionomers have been used as the base polymer for binding alkali, alkaline earth and transition metal ions. Organic amines such as n-hexylamine, hexamethylene tetraamine, 2,2,6,6-tetramethyM-hydroxy piperazine, ethylene diamine and polymeric diamines such as silicone diamine, polyether diamine and polymeric diamines such as silicone diamine, polyether diamine and polyamide oligomers considerably enhance the complex formation characteristics of Zn(II) ethylene ionomers thereby enhancing the physico-chemical properties [13]. [Pg.95]

We have used X-ray methods to compare the crystallite size of RIM specimens prepared with and without use of a polyether diamine (PEDA) additive. These results are compared with differential scanning calorimetry data on the hard domain melting behavior and dynamic-mechanical studies of the extent of phase separation. Mechanical data on flexural modulus, elongation, impact strength, and heat sag behavior have been obtained for the same specimens and have been correlated with the structural analyses. [Pg.54]

Sforfa ML, Yoshida IVP, Nunes SP (1999) Organic-inorganic membranes prepared Irom polyether diamine and epoxy silane. J Membr Sci 159(1-2) 197-207... [Pg.184]

Hycai Reactive Liquid Polymers Preliminary Data Sheet AB-16, Hycai Reactive Liquid Polymer Modified Epoxy Adhesives Polyether Diamine Hardeners, BFGoodrich, August 1983. [Pg.225]

Sforca, M.L, Yoshida, I.V.P., and Nunes, S.P. (1999) Oiganic-inorganic membranes prepared from polyether diamine and epoxy silane. /. Memb. ScL, 159,197- 2ff7. [Pg.1109]

To produce a spandex fiber by reaction spinning, a 1000—3500 molecular weight polyester or polyether glycol reacts with a diisocyanate at a molar ratio of about 1 2. The viscosity of this isocyanate-terrninated prepolymer may be adjusted by adding small amounts of an inert solvent, and then extmded into a coagulating bath that contains a diamine so that filament and polymer formation occur simultaneously. Reactions are completed as the filaments are cured and solvent evaporated on a belt dryer. After appHcation of a finish, the fibers are wound on tubes or bobbins and rewound if necessary to reduce interfiber cohesion. [Pg.307]

Curing Systems. The most commonly used vulcanizing agent for the polyethers not containing AGE, that is, ECH and ECH—EO, is 2-mercaptoimidazoline, also called ethylenethiourea [96-45-7]. Other commercially appHed curing agents include derivatives of 2,5-dimercapto-l,3,4-thiadiazole, trithiocyanuric acid and derivatives, bisphenols, diamines, and other substituted thioureas. [Pg.557]

As with the flexible foams there has been a shift to the use of polyethers. These are largely adducts based either on trifunctional hydroxy compounds, on tetrafunctional materials such as pentaerythritol or a hexafunctional material such as sorbitol. Ethylene diamine and, it is understood, domestic sugar are also employed. Where trifunctional materials are used these are of lower molecular weight (-500) than with the polyethers for flexible foams in order to reduce the distance between hydroxyl groups and hence increase the degree of cross-linking. [Pg.801]

The presence of ether linkages in the polymer molecule imparts chain flexibility, lowers glass transition temperature, and enhances solubility while maintaining the desired high temperature characteristics [192]. Recently, polyether imines were prepared by the reaction of different diamines with 4,4 -[l,4-phenylene bis(oxy)] bisbenzaldehyde [184]. The polymers synthesized by the solution method were yellow to white in color and had inherent viscosities up to 0.59 dl/g in concentrated H2SO4. Some of these polyimines can be considered as... [Pg.50]

The same sequence of reactions are used to prepare macrobicyclic diamines with polyether links.5-6 The reduction of macrobicyclic... [Pg.46]

This reaction is truly tempting because it potentially satisfies the need in the search for a way to reclaim the chemical value of a polyurethane recycle foam project [12, 13]. When a polyurethane foam is hydrolyzed, it gives aromatic diamine and polyether polyol, both in very crude forms. The diamine can be purified by regular means, but the crude polyether polyol cannot be easily cleaned up due to its polymeric nature. If this Ganem reaction can work well, the polyether polyol stream can be converted to a low-molecular-weight chemical, which can then be purified by conventional process such as distillation. Indeed, when this reaction was tried on a polyether triol of 3000 molecular weight as a model, the diacetate of propylene glycol was isolated by distillation. Unfortunately, the yield was too low to be of practical interest. [Pg.719]

One of the first examples of this type of blend was composed of SPEEK or SPES as the acidic component and diaminated PES, poly(4-vinylpyridine) (P4VP), poly(benzimidazole) (PBl), or poly(ethyleneimine) (PEI) as the basic component. " For blend lEC values of 1.0 meq/g, conductivity values were reported to be good, as was H2/O2 EC performance. Thermal stabilities for these blends was also demonstrated to be high (>270°C). Other examples of acid-base PEMs include blends of SPPO and PBI, sulfonated poly(phthalazinone ether ketone) and aminated SPES, SPIs and aminated Pls, and SPEEK with PES bearing benzimidazole side groups, ° as well as an unusual example in which the blend is composed of sulfonated, hyper-branched polyether and pyridine-functionalized polysulfone. ... [Pg.163]


See other pages where POLYETHER DIAMINE is mentioned: [Pg.536]    [Pg.239]    [Pg.34]    [Pg.536]    [Pg.114]    [Pg.53]    [Pg.56]    [Pg.306]    [Pg.20]    [Pg.301]    [Pg.1082]    [Pg.536]    [Pg.239]    [Pg.34]    [Pg.536]    [Pg.114]    [Pg.53]    [Pg.56]    [Pg.306]    [Pg.20]    [Pg.301]    [Pg.1082]    [Pg.304]    [Pg.306]    [Pg.348]    [Pg.351]    [Pg.189]    [Pg.347]    [Pg.8]    [Pg.18]    [Pg.192]    [Pg.201]    [Pg.255]    [Pg.448]    [Pg.49]    [Pg.6]    [Pg.151]    [Pg.186]    [Pg.264]    [Pg.398]    [Pg.111]    [Pg.552]    [Pg.33]    [Pg.131]    [Pg.435]    [Pg.285]    [Pg.390]   


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