Layered double hydroxides (LDH) with brucite like structure was modified with various anionic surfactants containing sulfonate, carboxyl, phosphonate and sulfate end group through ion-exchange method. XRD reports indicated that the sulfonate group containing surfactants led to an adsorption process whereas the sulfate, carboxyl and phosphonate group containing surfactant led to an intercalation process. This can be evidenced from the change in basal spacing of LDH. The presence of anionic surfactants in the LDH was supported by FTIR spectroscopy. The FTIR spectrum indicated that complete removal of carbonate anion from the inter layer space of LDH is very difficult. The phosphonate intercalated HT showed less thermal stability than pristine LDH.
Oxidative chemical polymerization of aniline was carried out using peroxydisulphate and peroxomonosulphate as a lone initiator in an aqueous acidic medium in the presence of Rayon fiber. The Rayon fiber was tested for the chemical grafting of polyaniline onto it. The content of polyaniline (wt %) in the backbone was found to vary while varying the [M], [I], and (amount of Rayon fiber) during the polymerization of aniline. Various graft parameters like rate of grafting, % grafting, and % efficiency were calculated. Rate of homopolymerization was also followed for both cases. The chemical grafting was confirmed using FTIR spectroscopy, cyclic voltammetry, weight loss study, and conductivity measurements. Probable mechanism has been proposed to explain the experimental results obtained.
ABSTRACT:The chemistry of free-radical graft copolymerization initiated with peroxomonosulfate (PMS)-thioglycolic acid (TGA) redox system has been investigated by using 4-vinyl pyridine (4VP) as a model for nylon 6 fiber in aqueous solution under nitrogen atmosphere. Effects of concentration of 4VP, PMS, TGA, nylon 6, time, and temperature on R h and graft parameters were studied. The FTIR spectrum of nylon 6-g-4VP was reported. Water retention capacity (WRC) of the grafted fiber was tested.
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