Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Cure-Rite® IBT

COMPOUND NAME, PAGE Activator OT Urea, 37 Markstat 51,263 Markstat 51,264 Markstat 51,265 Cyanox STDP, 81 Cyanox LTDP, 79 Stearic Acid, 313 Polycizer Butyl Oleate, 287 Butyl ricinoleate, 195 Flexol EP-8, 231 Flexol EP-8, 233 Flexol EP-8, 232 Epoxidized linseed oil, 229 Epoxidized linseed oil, 227 Epoxidized linseed oil, 228 Cure-Rite IBT, 35 Dioctyl maleate, 223 Isonox 232, 111 Ethaphos 368, 95 Alkanox P27, 63 Kemamide E ultra, 309 Citroflex B-6, 209 Laurex , 261 Retarder AK, 311 Santicizer 278, 155 Perkacit DPG, 305... [Pg.471]

Westco TIBTD, see Cure-Rite IBT, 38 Wingstay S see Naugard 635, 172 WingStay L, see Lowinox CPL, 58 Witamol 500, 386-387 Witcizer 100, see Polycizer Butyl oleate, 364... [Pg.617]

COMPOUND NAME, PAGE Activator OT Urea, 41 Markstat 51, 345 Markstat 51, 346 Markstat 51, 347 Cyanox STDP, 109 Cyanox LTDP, 107 Stearic Acid, 409 Poiycizer Butyi Oieate, 371 Dimethyi sebacate, 263 Butyi ricinoieate, 315 Fiexoi EP-8, 279 Fiexoi EP-8, 281 Fiexoi EP-8, 280 Epoxidized iinseed oii, 271 Epoxidized iinseed oii, 269 Epoxidized iinseed oii, 270 Cure-Rite IBT, 39 Dioctyi maieate, 265 lsonox 232, 161 Ethaphos 368, 143 Ethaphos 368, 141 Aikanox P27, 67 Kemamide E uitra, 405... [Pg.619]

Cure-Rite IBM and Cure-Rite IBT from B.F.Goodrich, a thiuram monosulphide and disulphide, respectively, based upon diisobutylamine, are new low nitrosamine-producing accelerators. These additives, together with other commercial thiuram compounds, were compared as co-accelerators for benzothiazole sulphenamides in SBR/polybutadiene and NR compounds. The effects that these thiurams had on the scorch safety and cure rates during curing and on the reversion resistance of the vulcanisates were demonstrated. Cure-Rite IBM excelled in improving the scorch safety of the benzothiazole while improving the cure rates. Cure-Rite IBT appeared to be a... [Pg.55]

Two thiuram accelerators developed by Goodrich, Cure-rite IBM tetraisobutylthiuram monosulphide and Cure-rite IBT tetraisobutylthiuram disulphide, were evaluated along with other commercial thiurams as co-accelerators for benzothiazole sulphenamides in the vulcanisation of NR and SBR/polybutadiene tyre compounds. The effects of these thiurams on scorch safety and cure rates during vulcanisation and on the reversion resistance of vulcanisates were investigated, and differences in the types of sulphur crosslinks developed by the various thiurams were examined. 6 refs. [Pg.81]


See other pages where Cure-Rite® IBT is mentioned: [Pg.34]    [Pg.35]    [Pg.341]    [Pg.39]    [Pg.40]    [Pg.447]    [Pg.644]    [Pg.34]    [Pg.35]    [Pg.341]    [Pg.39]    [Pg.40]    [Pg.447]    [Pg.644]   
See also in sourсe #XX -- [ Pg.34 ]

See also in sourсe #XX -- [ Pg.38 ]




SEARCH



© 2024 chempedia.info