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John H. P. Tyman

Researcher at Brunel University London

Publications -  87
Citations -  1142

John H. P. Tyman is an academic researcher from Brunel University London. The author has contributed to research in topics: Cardanol & Carminic acid. The author has an hindex of 17, co-authored 87 publications receiving 1089 citations. Previous affiliations of John H. P. Tyman include Royal Free Hospital.

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The UV–visible absorption and fluorescence of some substituted 1,8-naphthalimides and naphthalic anhydrides

Abstract: A number of substituted 1,8-naphthalimides and naphthalic anhydrides have been prepared and their absorption and fluorescence properties in absolute ethanol have been determined. In the absence of an alkylamino substituent in the naphthalene ring, the compounds are colourless and weakly fluorescent. In the presence of such a substituent they become yellow and frequently fluoresce strongly with quantum yields of the order of 0.8.
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The extraction of natural cashew nut-shell liquid from the cashew nut (Anacardium occidentale).

TL;DR: In the two-stage recovery of natural cashew nut-shell liquid by solvent extraction, the overall yields from half-shells obtained by mechanical cutting and from chilled fragmented shells (to solidify the phenols) by manual processing are identical, indicating that no physical loss of phenolic material occurs in the mechanical process as mentioned in this paper.
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Synthesis and characterization of polyethoxylate surfactants derived from phenolic lipids

TL;DR: In this article, polyethoxylates from cardanol and from cardol, the main component phenolic lipids in technical cashew nutshell liquid derived from the replenishable source Anacardium occidentale, were obtained by reaction with ethylene oxide under base-catalyzed conditions.
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Surfactant properties and biodegradation of polyethoxylates from phenolic lipids

TL;DR: In this article, the surface tension of aqueous solutions of cardanol and cardol polyethoxylates derived from technical cashew nut-shell liquid were examined to determine their relative surfactancy.
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The synthesis and fluorescence of novel N-substituted-1,8-naphthylimides

TL;DR: In this paper, the synthesis and characterisation of a series of novel 4-acylamino and 4-alkylamino-N-1,8-naphthalimides is described.