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Cyclohexyl benzothiazole sulphenamid

Barnes et al developed an LC-MS method to identify vulcanisation agents and their breakdown products in food and drink samples. A large sample of 236 retail foodstuffs were analysed for the presence of 2-mercaptobenzothiazole (MBT) and its breakdown product mercapto-benzothiazole (MB). The accelerators 2-mercaptobenzothiazyl (MBTS) and A-cyclohexyl-2-benzothiazole sulphenamide (CBS), which are commonly used in food contact rubbers, were also looked for. MBT and MB are also known to be breakdown products of these two compounds. The detection limit for these species was found to depend on the food product type and ranged from 0.005-0.043 mg/kg. No MBT, MB, MBTS or CBS were detected in any of the samples above these levels. [Pg.292]

Hilton and Altenau and Hayes and Altenau used mass spectrometry to qualitatively identify volatile antioxidants in sheet samples of synthetic styrene-butadiene rubbers and rubber type vulcanizates. They extracted the polymer with acetone in a Sohxlet apparatus, removed excess solvent and dissolved the residue in benzene. Substances identified and determined by this procedure include N-phenyl-fi-napthylamine, 6-dodecyl-2,2,4-trimethyl 1,2-dihydroquinolines, trisnonyl-phenyl-phosphite, isobutylene - bisphenol A reaction product, 2-mercaptobenzothiazole sulphen-amide (accelerator) N-cyclohexyl-2-benzothiazole sulphenamide, N-tert-butyl-2-benzo-thiazole sulphenamide, 2-(4-morpolinothio) benzothiazole, 2-(2,6-dimethyl-morphal-inothio) benzothiazole, N,N -diisopropyl 2-benzothiazoles, 2-mercaptobenzo-thiazole and N,N -dicyclohexyl-2-benzothiazole sulphamide. [Pg.71]

Investigations were carried out with the binary combinations of each of bis(N-methylpiperazino)thiuram disulphide, tetrabenzylthiuram disulphide, and tetramethylthiuram disulphide, separately with N-cyclohexyl-2-benzothiazole sulphenamide, 2-mercaptobenzothiazole, and 2-mercaptobenzothiazyl disulphide in the combinations studied. 19 refs. [Pg.124]

Tetraisobutylthiuram monosulphide (TiBTM) was evaluated as a retarder and secondary accelerator for both N-t-butyl-2-benzothiazole sulphenamide and N-cyclohexyl-2-benzothiazole sulphenamide in SBR/ polybutadiene and NR compounds. TiBTM was also compared in these systems to the retarder N-cyclohexyl thiophthalimide (CTP) and the secondary accelerator tetramethylthiuram monosulphide (TMTM). When used at low levels with sulphenamide accelerators, TiBTM could extend the scorch time by 2-3 minutes and then increase the cure rate beyond that of the primary accelerator. The extent of these effects was influenced by the types of rubber and sulphenamide. At low levels TiBTM performed as an equivalent substitute for a CTP/... [Pg.128]

The effects of using cetyltrimethylammonium maleate(CTMAM) and N-cyclohexyl-2-benzothiazole-2-sulphenamide(CBS) as accelerators in carbon black-filled NR compounds were studied. The results obtained showed that cure time and scorch time were faster for CTMAM... [Pg.54]


See other pages where Cyclohexyl benzothiazole sulphenamid is mentioned: [Pg.170]    [Pg.170]    [Pg.762]    [Pg.79]    [Pg.157]    [Pg.389]    [Pg.413]    [Pg.357]   
See also in sourсe #XX -- [ Pg.170 ]




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Benzothiazole

Benzothiazole sulphenamide

Benzothiazoles

Cyclohexyl

Cyclohexylation

Sulphenamides

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