Abstract: A viscometer having a substantially horizontal reservoir including a trap for retaining a sample indefinitely in the reservoir. A substantially vertical measuring tube disposed perpendicularly to the substantially horizontal reservoir and depends substantially upwardly from the reservoir. A junction interconnects the trap, a generally downwardly projecting fill tube, and a generally upwardly projecting vent tube.

Abstract: A polyurethane obtained by reaction between (i) at least one homopolymer obtained by homopolymerization of ?-caprolactone, and (ii) at least one dissocyanate, wherein said reaction between (i) and (ii) and said homopolymerization are performed in presence of a catalyst selected from (a) a catalyst containing bismuth ethylhexanoate and ethylhexanoic acid, (b) a catalyst containing bismuth ethylhexanoate and bismuth neodecanoate, and (c) a catalyst containing zinc neodecanoate and zinc oxide.

Abstract: A viscometer having a substantially horizontal reservoir including a trap for retaining a sample indefinitely in the reservoir. A substantially vertical measuring tube disposed perpendicularly to the substantially horizontal reservoir and depends substantially upwardly from the reservoir. A junction interconnects the trap, a generally downwardly projecting fill tube, and a generally upwardly projecting vent tube.

Abstract: A polyurethane obtained by reaction between (i) at least one homopolymer obtained by homopolymerisation of ?-caprolactone, and (ii) at least one dissocyanate, wherein said reaction between (i) and (ii) and said homopolymerisation are performed in presence of a catalyst selected from (a) a catalyst containing bismuth ethylhexanoate and ethylhexanoic acid, (b) a catalyst containing bismuth ethylhexanoate and bismuth neodecanoate, and (c) a catalyst containing zinc neodecanoate and zinc oxide.

Abstract: The present invention provides a composition wherein a homo-polymer or copolymer of caprolactone has been produced by polymerising caprolactone, optionally with a co-monomer, in the presence of a polymerisation catalyst and an initiator, and the use of such a composition according for the manufacture of a polyurethane. The present invention further provides a process for the production of a homopolymer or a co-polymer of caprolactone comprising polymerising a composition comprising: (i) at least one caprolactone monomer and optionally a co-monomer; and (ii) a catalyst comprising (a) bismuth ethylhexanoate and ethylhexanoic acid, (b) bismuth ethylhexanoate and bismuth neodecanoate, or (c) zinc neodecanoate and zinc oxide.

Abstract: A method for the preparation of an amine-terminated caprolactone polymer having at least two terminal ends with a primary amine located thereon, comprising the steps of: (a) using a polycarboxylic acid as an initiator in the ring opening poly- merization of epsilon-caprolactone to produce a polycaprolactone polymer having at least two terminal ends with a carboxylic acid located thereon; and then (b) reacting the product of step (a) with a polyamine at a temperature of above 50° C. to produce an amine-terminated polycaprolactone polymer.

Abstract: This invention relates to a composition comprising antimony trifluoride and silica, a method for the preparation of said composition and use of said composition as a catalyst in a process for the oxidation of cyclohexanone to &egr;-caprolactone.

Abstract: Process for the production of an aqueous monoester peroxycarboxylic acid solution by reaction of a peroxygen compound with at least one dicarboxylic acid and with at least one alcohol optionally in the presence of an acid catalyst. Aqueous monoester peroxycarboxylic acid solution obtainable by this process. Use of the aqueous monoester peroxycarboxylic acid solution as disinfectant.

Abstract: This invention relates to a composition comprising antimony trifluoride and silica, a method for the preparation of said composition and use of said composition as a catalyst.

Abstract: Storage stable aqueous acidic solutions, often having a pH of up to 1 containing an ester peracid and/or an acid peracid can be obtained by reacting a diester satisfying the general formula R1—O—CO—R2—CO—O—R3 in which R1 and R3 each represents a alkyl group containing from 1 to 4 carbon atoms which may the same of different and R2 represents an aliphatic alkylene group optionally unsaturated which may be linear or branched containing from 2 to 6 carbon atoms with aqueous hydrogen peroxide in the presence of an acid, such as sulphuric acid and permitting the compositions to progress towards equilibrium concentrations. By starting with a diester, perhydrolysis generates an ester peracid which is a particularly effective peracid. The process can be controlled to produce solutions containing a high peracid content and within a wide range of ratios of ester peracid to acid peracid.

Abstract: Storage stable, aqueous acidic solutions having a pH in the range of from 1 to 5 comprising at least one ester peracid having general formula where R represents an alkyl group having from 1 to 4 carbons and x equals 1 to 4, are provided. The solutions can be prepared by contacting an aqueous solution of a carboxylic compound having general formula where x is from 1 to 4 and R represents an alkyl group having from 1 to 4 carbons with an inorganic peroxygen compound, preferably hydrogen peroxide, at a pH of less than 4 until at least some ester peracid is produced, and thereafter adjusting the pH to be in the range of from 1 to 5, if necessary.

Abstract: Peroxycarboxylic acids of formula (I) are disclosed wherein the substituents are defined by the disclosure. The peroxycarboxylic acids are useful for washing, bleaching and disinfecting, and methods for using them in such processes are also disclosed. Further, a process for preparing the peroxycarboxylic acids is disclosed.

Abstract: In one class of processes for making poorly soluble organic peroxyacids the corresponding carboxylic acid is reacted with hydrogen peroxide in a reaction medium containing a high concentration of sulphuric acid. The presence of such constituents in the reaction mixture and the manner of the reactants and the way in which they are brought into contact, can result in the processes being hazardous. In the present invention, hazard problems are reduced or eliminated by first dissolving the carboxylic acid in concentrated sulphuric acid, secondly forming a Caro's acid solution containing a complementary amount of sulphuric acid and hydrogen peroxide within a predetermined range, and then introducing the carboxylic acid solution at a controlled rate in the Caro's acid solution, often over a period of from about 30 to 90 minutes, with agitation and temperature control.