Topic
Triphenyl phosphate
About: Triphenyl phosphate is a research topic. Over the lifetime, 579 publications have been published within this topic receiving 6681 citations. The topic is also known as: phenyl phosphate & TPP.
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35 citations
TL;DR: In this paper, the effect of bisphenol A bis(diphenyl phosphate) oligomer (BDP) on the limiting oxygen index test method and thermal decomposition of poly(butylene terephthalate) (PBT) was studied.
34 citations
TL;DR: In this article, the influence of metallic and oxidized iron/steel on the reactivity of triphenyl phosphorothionate (TPPT) in oil solution at 473 K was investigated by means of FT-IR, NMR and XPS.
34 citations
TL;DR: Aromatic phosphate esters such as triphenyl phosphate, tricresyl phosphate (TCP), and tri(tert-butylphenyl) phosphate, have been degraded in the presence of pure iron or metal alloys such as M-50 or 52100 steel as discussed by the authors.
Abstract: Aromatic phosphate esters such as triphenyl phosphate, tricresyl phosphate (TCP), and tri(tert-butylphenyl) phosphate, have been degraded in the presence of pure iron or metal alloys such as M-50 or 52100 steel. Among these volatile degradation products are those generated from the addition of an aromatic ring to the phosphate ester. Other products, which have been identified, include substituted biphenyls and diphenyl ethers derived from the decomposition of the above-mentioned addition product. Still other products are fused ring aromatic compounds such as anthracene, which arise from secondary reactions of the initial decomposition reactions. The decomposition reactions leave a nonvolatile phosphate film on the surface of the metal. Characterization of the film with Auger spectroscopy suggests iron phosphate as the product. X-ray photoelectron spectroscopy shows the presence of a bound organic layer at the surface. A mechanism that explains many of the decomposition products and the formation of a boun...
33 citations
TL;DR: In this paper, the reactivity of triphenyl phosphorothionate (TPPT) in lubricant oil solution at high temperature (423 and 473 K) has been studied by Fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance (NMR).
Abstract: Investigating the thermo-oxidative reactivity of anti-wear additives in lubricant oil solution at high temperature can significantly contribute to an understanding of the mechanism of thermal film and tribofilm formation on metal surfaces. In this study, the reactivity of triphenyl phosphorothionate (TPPT) in lubricant oil solution at high temperature (423 and 473 K) has been studied by Fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance (NMR) spectroscopy. The results show that the TPPT molecule was highly thermally stable and did not completely decompose in oil solution even upon heating at 423 K for 168 h and at 473 K for 72 h. The degradation of the TPPT molecule, which turned out to be a first-order reaction, started taking place after 6 h at both temperatures, leading to the breakage of the P=S bond with the formation of triphenyl phosphate. During these heating experiments, no oil-insoluble compounds were detected. The oxidation of the base oil as a result of the prolonged heating demonstrated that the TPPT molecule did not effectively act as oxidation inhibitor.
32 citations