CPE

Cm.ORINE OXYGEN ACIDS AND SALTS - CIE.ORIC ACID AND CPE ORATES] (Vol 5)... 

Heat stabilizers protect polymers from the chemical degrading effects of heat or uv irradiation. These additives include a wide variety of chemical substances, ranging from purely organic chemicals to metallic soaps to complex organometaUic compounds. By far the most common polymer requiring the use of heat stabilizers is poly(vinyl chloride) (PVC). However, copolymers of PVC, chlorinated poly(vinyl chloride) (CPVC), poly(vinyhdene chloride) (PVDC), and chlorinated polyethylene (CPE), also benefit from this technology. Without the use of heat stabilizers, PVC could not be the widely used polymer that it is, with worldwide production of nearly 16 million metric tons in 1991 alone (see Vinyl polymers). 

Fig. 10. Preparation and morphology of toughened PVC (a) secondary PVC grain (50—250 flm) (b) modified PVC with coherent primary grain (ca 1 -lm) (220). CPE = chlorinated polyethylene EVA = ethylene—vinyl acetate copolymers ABS = acrylonitrile—butadiene—styrene MBS = methyl...

J. E. Potts and co-workers. Polymers and Ecological Problems, Plenum Press, New York, 1973 EPA Contract, CPE-70-124 U.S. Environmental Protection Agency, Washington, D.C., 1972. 

Thermoplastics. There are five elastomeric membranes that are thermoplastic. Two materials, chlorinated polyethylene (CPE) and polyisobutylene (PIB), are relatively obscure. Thermoplastic materials can be either heat-fused or solvent-welded. In contrast to Hypalon and uncured EPDM, this abiHty to fuse the membranes together remains throughout the life of the material. However, cleaning of the membrane surface after exposure to weather is required. Correct cleaning procedures for specific membranes are available from the individual manufacturer. 

Chlorinated polyethylene (CPE) has excellent o2one, oil, and heat resistance. In addition chlorinated polyethylene has replaced chloroprene elastomers. CPE has a lower specific gravity than chloroprene compounds and produces compounds that are similar to CR in properties but with lower costs. In addition, due to high levels of chlorine in the polymer, the flame resistance of the compounds of CPE are high. 

DuPont—Dow is the primary suppHer of these polymers. There is an estimated 18,000 t of these elastomers used per year. The main uses of CPE are in constmction, automotive, and electrical appHcations. These include power steering hose, electrical cords used in low voltage appHcations (extension cords, ignition wire), pond liners, and as a plastic modifier to improve impact modification. 

It is estimated that 27,000 t/yr of CSM have been commercially used in the United States. However, due to environmental problems in the manufacturing process, it has been necessary to develop a process that is much mote expensive. As a result many companies using CSM ate trying to replace the CSM with CPE or other elastomers. The result is a decline in the usage of this polymer. Chlorosulfonated polyethylene is sold under the trade name Hypalon (DuPont—Dow Company). 

Among other polymers used in this market, EPDM (30%) leads foHowed by PVC/PVC aUoys (5%), and CSPE/CPE (3%). Modified bitumen (20%) and metal (10%) have the remainder of the market. Single-ply material systems including PVC/PVC aHoys, EPDM, and CSPE/CPE are gaining share, with PVC expected to grow at about 5—6%/yr over the next five years. 

ECTN Association, ESCPE Lyon, Erance mimero echemtest. net smith cpe.fr ECTN Association, University of Dortmund, Germany E-mail mitchell eurobachelor.net... 

Sodium dodecylsulphate was selected as an anionic surfactant Factors affecting acid-induced cloud point extraction including surfactant, hydrochloric acid, PAHs, and electrolyte concentration, centrifugation have been examined. Finally, we applied the optimized acid-induced CPE system for combination of the extraction and preconcentration steps with fluorimetric determination of some representatives of PAHs. Suggested means was used for PAHs determination in tap water. 

Scheme 2 Reaction scheme for the formation of block copolymer between OPS and CPE.

ATBN - amine terminated nitrile rubber X - Flory Huggins interaction parameter CPE - carboxylated polyethylene d - width at half height of the copolymer profile given by Kuhn statistical segment length DMAE - dimethyl amino ethanol r - interfacial tension reduction d - particle size reduction DSC - differential scanning calorimetry EMA - ethylene methyl acrylate copolymer ENR - epoxidized natural rubber EOR - ethylene olefin rubber EPDM - ethylene propylene diene monomer EPM - ethylene propylene monomer rubber EPR - ethylene propylene rubber EPR-g-SA - succinic anhydride grafted ethylene propylene rubber... 

CKOJibKy Kij = Kji, OTCioAa nojiy iaeM onpeAejisroinHe ypaBHeHHH ojifi cjKHMaeMofl ynpyroH cpe ibi ... 

Phc. 3.5. XapaKTepHCTHKH KBaannonepeiiHOH npocrofi bojihh ( 2 BoapacTaer Ri — cpe a naxoAHTca b noKoe). 

The equivalent circuit of a section of this SEI is presented in Fig. 13(b). It was recently found [123, 124] that at temperatures lower than 90 °C, the grain-boundary resistance of composite polymer electrolytes and composite solid electrolytes based on Lil-A Ojis many times larger than their ionic resistance. At 30 °C / GB is several orders of magnitude larger than (the ionic resistance) and for 100 pm-thick CPE foils or Lil-A Oj pellets it reaches [125] 105-106Qcm2 (depending on CPE composition). 

A value of Rqb for an SEI lOnm thick can be estimated from its values for CPE and CSE by assuming that these solid electrolytes consist of nanometer-sized particles. Thus the expected value for / GB at 30 °C for a lOnm SEI is in the range 10-lOOQcm2, i.e., it cannot be neglected. In some cases it may be larger than the ionic (bulk) resistance of the SEI. This calculation leads us to the conclusion that 7 GB and CGB must be included in the equivalent circuits of the SEI, for both metallic lithium and for LixC6 electrodes. The equivalent circuit for a mosaic-type... 

At temperatures above or near the eutectic temperature of the polymer phase, CSEi values are typically in the range of 0.1-2 pFcm-2 [5], However, for stiff CPEs or below this temperature, CSEI can be as low as 0.001 pFcm 2 (Fig. 16). When a CPE is cooled from 100 °C to 50 °C, the CSE1 falls by a factor of 2-3, and on reheating to 100 °C it returns to its previous value. This is an indication of void formation at the Li/CPE interface. As a result, the apparent energy of activation for ionic conduction in the SEI cannot be calculated from Arrhenius plots of 1// sei but rather from Arrhenius plots of 7SE)... 

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