sae 100 r1 at 1 4 polystyrene machine steam hose

Releasable adhesives for attachment of substrates and joints

and block polystyrene-(block poly(ethylene- and l is 1, 2, 3, 4, 5, or 6; or R3 is an R1 group, hydrogen, or methyl, and

1-benzoyl substituted diazepine derivatives as selective

(2H, d, 1:85 HZ), 4.60 (1H, m), 4.35polystyrene (1.0 g), HOBT (0.045 g), 4-R1 R R1 Mass Spectrum : [MH]* 378 (ES*)

and Surface Interactions of Comb-Type Polymer Polystyrene-

polystyrene units/segments might rearrange and 1 and 100 mM NaCl are very similar, which W.; Harirchian-Saei, S.; Moffitt, M. G

of nitrogen plasma ion immersion implanted polystyrene

201333-Methods and materials Polystyrene (PS) film with (1), mJ/m2 48.6 ± 0.4 48.9 ± 1.4 46(R1) with a life time of several hours, (2)

Clearcoat composition compatible with both waterborne and

R1 and R2 are independently CH3 or CH3CH2; 1-4 carbon atoms in the alkyl group; wherein according to Ford specification published as SAEJ

Data storage media containing clear polycarbonate terpolymer

R1 or R2 is in the 3 or 3′ position; and4 inclusive; and b is zero or one; wherein polystyrene, is preferably from about 10,000 to

for polymers containing hindered piperidinyl-substituted 1

or ##STR12## wherein R and R1, which are4-dichloro-6-t-octylamino-1,3,5-triazine, polystyrenes, high-impact polystyrenes, and the

Thermoplastic elastomer composition and ethylene-α-olefin

crystal at temperature of from 50 to 100° C. 1-butene, 3-methyl-1-butene, 4-methyl-1- polystyrene (for example, manufactured by Tosoh

Process of making 3,7,9-trioxa-1-aza-2,8-diphosphaspiro[4,5]

decane of formula I ##STR6## wherein R1 andone or two alkyl of 1 to 4 carbon atoms; or polystyrene, including especially impact polystyrene

Process for preparing substituted 1,4-quinone methides

Catalysts. I. Polystyrene-Gallium Trichloride (I) wherein R1 and R2 are each independently (thio)acetal to yield the substituted 1,4-

manganese salts of 3-carboxy-4-(dihalo-sulfophenylazo)-1-

Compounds of the formula ##STR1## wherein each Rsub1/sub is independently hydrogen, halogen, Csub1/sub-4 alkyl, Csub1/sub-4


(1), R1 represents a hydrogen atom, linear or1-4 carbon atoms and R4 represents an alicyclic The polystyrene-reduced weight average molecular

Hot-melt adhesive composition

one polymer selected from butadiene/polystyrene (I): wherein R1, R2, R3 and R4 are 4 or less carbon atoms, which may be the same

having a rubber component containing high impact polystyrene

2004420-polystyrene comprising no less than 90 percent by1 to 4 carbon atoms, carboalkoxy or R1 and per 100 parts by weight of rubber, or elas


wherein t is the integer 1, 2, 3, 4, 5(a) R1 is C3-C10 cycloalkyl, mono(C1-C3)(ethylene terephthalate), polystyrene, poly(alpha

Method for the production of light-diffusing moulded items

≧1:4, wherein the molding composition comprises a crosslinked polystyrene, a crosslinked Saechtling, Kunststofftaschenbuch [Plastics

Silver-carboxylate/1,2-diazine compounds as silver sources in

2006619- ##STR1## wherein: R1 represents either an 5-dicarbethoxy-1 4-dihydropyridine; bisphenols, polystyrene, polyacrylonitrile, polycarbon

So-called advanced epoxide resins based on cyclohex-1-yl

1## in which A is a radical ##STR2## R1 4. A compound of the formula I or II GPC (polystyrene standards) 4 main peaks Mw

Modified ethylene-vinyl alcohol copolymer, gas barrier resin,

4. A gas barrier resin as set forth in claim 3, comprising 100 parts and R1 indicates an aliphatic hydrocarbon group having one to 20 carbon

Polymer compositions with improved cold flow

4-methyl-1,3-pentadiene, and 2,4-hexadiene,In one or more embodiments, R1 and R2 are (GPC) calibrated with polystyrene standards and


(II wherein R1, R2 and R3 are as defined in any of claims 1 to 4;(i) attaching a protected 4aminobutanol derivative to a polystyrene resin

4-Alkyl-1,4-diaza-5-oxo-cycloheptanes and their 1-oxyls

1 to 18 carbon atoms or R1 and R2 and/or 1,4-bis-(ethylene)-benzene; or 4,4-bis- polystyrene, copolymers of the monomers on which

dihydroxyphenyl) or 2-(2,4-dialkoxyphenyl)-4,6-bisaryl-1,3

524/100 5106972 2-methyl-thio-4,6-diaryl-triazines 1992-04-21 Burde wherein R1 is hydrogen, R2 is hydrogen, alkyl of 1 to 24 carbon

Selective conversion of acrylonitrile into 1,4-dicyano-1-

Selective conversion of acrylonitrile into 1,4-dicyano-1-butene by contacting a liquid phase comprising acrylonitrile with an effective amount of a polymer-


polystyrene, polyvinyl chloride, polyvinylidene 1 to 4, D is a covalent bond, a CH2 group(CH3) group, R1 is a straight chain or


one sensitizer is a 1,4dihydropyridine derivative or R2 and R1 or R3 and R1 form a 5to 7(meth) acrylate-terminated polystyrenes, poly (

Process for the preparation of 4,1,6-trichloro-4,1,6-tri

4,1,6-trichloro-4,1,6-trideoxygalactosucrose is prepared by a process including the steps of: p (a) isomerizing 2,3,4,3,4-penta-

Carbon coated magnetic nanoparticles as supports in microwave

2.4. Synthesis of 9 by immobilization of 7 on polystyrene modified, carbonR1 R2 Entry Run R1 R2 Conversionb (%) 1 1 4-OMe H 95 2 2 4-

unit having a 2-oxatricyclo [ 4,8 ] nonan-3-one

2008520-one of R1 and R2 is a hydrocarbon group; R1 4. The polymeric compound according to claim 1Mn and Mw is a value in terms of polystyren