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Zinc sulphide retarders

Birefringent retarders are made of anisotropic uniaxial crystals such as calcite, a-quartz, sapphire, zinc sulphide, cadmium selenide and others. As Eq. (3.2-14) shows, the produced retardation is exact for a definite wavenumber or for its multiples. Between them all remaining possible polarization states are passed through. [Pg.95]

Antimony trioxide has a synergistic effect with most halogenated FRs. It is also used in plasticized PVC because of its synergy with chlorine. Antimony oxide should not be used if translucency is required. In some cases ferric oxide is used in its place, for similar physical properties but improved electrical properties. It has been shown by extensive research to be non-carcinogenic. For polymers apart from PVC. a 50% replacement of antimony trioxide is possible with virtually all polymer systems. In particular with both plain and glass-reinforced nylons, excellent flame retardation can be achieved with a suitable combination of zinc sulphide and melamine cyanurate, eliminating both halogens and antimony trioxide. [Pg.120]

Antimony trioxide (SbaOj). It is produced from stibnite (antimony sulphide). Some typical properties are density 5.2-5.67 g/cm- pH of water suspension 2-6.5 particle size 0.2-3 p,m specific surface area 2-13 m-/g. Antimony trioxide has been the oxide universally employed as flame retardant, but recently antimony pentoxide (SbaOs) has also been used. Antimony oxides require the presence of a halogen compound to exert their fire-retardant effect. The flame-retarding action is produced in the vapour phase above the burning surface. The halogen and the antimony oxide in a vapour phase (above 315 C) react to form halides and oxyhalides which act as extinguishing moieties. Combination with zinc borate, zinc stannate and ammonium octamolybdate enhances the flame-retarding properties of antimony trioxide. [Pg.637]

Accelerators guanidines, thiazoles. sulphenamides, dithiocarbamates, thiuram sulphides, xanthates, aldehydeamines retarders phthalic anhydride, N-nitroso diphenylamine activators zinc oxide/stearic acid... [Pg.232]

With the sulphur-modified polymers cure may be brought about by zinc oxide and magnesium oxide in combination either alone or together with an accelerator such as ethylene thiourea. In the case of the homopolymers it has been common practice to support the zinc oxide/magnesium oxide/ethylene thiourea system with a further component. This component consists of a sulphide or a blend of sulphides of the type more commonly used as accelerators for the diene hydrocarbon polymers. These include mercaptobenzothiazole disulphide (MBTS), diorthotolyl guanidine (DOTG) and tetramethyl thiuram monosulphide (TMTM). In the polychloroprene homopolymers these materials appear to act as retarders of cure at processing temperatures but are accelerators at vulcanization temperatures. Their mechanism does not appear to have been fully elucidated. [Pg.305]

The beneficial effects of Ce02 are also reported in the literature. It was found that sulphidation of FeAl alloys was retarded because the nanoparticles inhibit iron diffusion and act as traps for the sulphur ions [26]. Cabot and Foissy also demonstrated that silica layers stabilised with CeOz nanoparticles led to significant improvements in the corrosion resistance of zinc-coated steels [27]. Cerium oxides are also reported as having a pronounced stabilising effect on the passive state of steels and then-corrosion resistance [28]. [Pg.77]


See other pages where Zinc sulphide retarders is mentioned: [Pg.125]    [Pg.184]    [Pg.48]    [Pg.271]   
See also in sourсe #XX -- [ Pg.95 ]




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