81 results about "Arylsulfonic Acids" patented technology

An enhanced activity aqueous disinfecting solution having a pH of from about 0.5 to about 6 and consisting essentially of (i) hydrogen peroxide in a concentration of from about 0.05 to about 8 w / w % of the solution; (ii) at least one anionic surfactant selected from the group consisting of C8 to C16 alkyl aryl sulfonic acids and alkali metal, ammonium, ethanolamine, calcium and magnesium salts thereof, sulfonated C12 to C22 carboxylic acids and alkali metal, ammonium, calcium and magnesium salts thereof, C6 to C22 alkyl diphenyl oxide sulfonic acids and alkali metal, ammonium, ethanolamine, calcium and magnesium salts thereof, naphthalene sulfonic acids and alkali metal, ammonium, calcium and magnesium salts thereof, C8 to C22 alkyl sulfonic acids and alkali metal, ammonium, calcium and magnesium salts thereof, alkali metal, ammonium, calcium and magnesium C8 to C18 alkyl sulfates, alkyl or alkenyl esters or diesters of sulfosuccinic acid in which the alkyl or alkenyl groups independently contain from six to eighteen carbon atoms and alkali metal, ammonium, calcium and magnesium salts thereof, and mixtures thereof, in a concentration range of from about 0.02 to about 8 w / w % of the solution. Optionally, the solution may contain (iii) at least one additional ingredient chosen from a monocarboxylic acid, a polycarboxylic acid, and mixtures thereof, in a concentration of from about 0.05 to about 4 w / w % of the solution; and (iv) at least one further additional ingredient chosen from benzyl alcohol, an alcohol comprising one to six carbon atoms, and mixtures thereof, in a concentration of from about 0.1 to about 10 w / w % of the solution.

An enhanced activity aqueous disinfecting solution having a pH of from about 0.5 to about 6 and consisting essentially of (i) hydrogen peroxide in a concentration of from about 0.05 to about 8 w / w % of the solution; (ii) at least one anionic surfactant selected from the group consisting of C8 to C16 alkyl aryl sulfonic acids and alkali metal, ammonium, ethanolamine, calcium and magnesium salts thereof, sulfonated C12 to C22 carboxylic acids and alkali metal, ammonium, calcium and magnesium salts thereof, C6 to C22 alkyl diphenyl oxide sulfonic acids and alkali metal, ammonium, ethanolamine, calcium and magnesium salts thereof, naphthalene sulfonic acids and alkali metal, ammonium, calcium and magnesium salts thereof, C8 to C22 alkyl sulfonic acids and alkali metal, ammonium, calcium and magnesium salts thereof, alkali metal, ammonium, calcium and magnesium C8 to C18 alkyl sulfates, alkyl or alkenyl esters or diesters of sulfosuccinic acid in which the alkyl or alkenyl groups independently contain from six to eighteen carbon atoms and alkali metal, ammonium, calcium and magnesium salts thereof, and mixtures thereof, in a concentration range of from about 0.02 to about 8 w / w % of the solution. Optionally, the solution may contain (iii) at least one additional ingredient chosen from a monocarboxylic acid, a polycarboxylic acid, and mixtures thereof, in a concentration of from about 0.05 to about 4 w / w % of the solution; and (iv) at least one further additional ingredient chosen from benzyl alcohol, an alcohol comprising one to six carbon atoms, and mixtures thereof, in a concentration of from about 0.1 to about 10 w / w % of the solution.

A silsesquioxane resin comprised of the units (Ph(CH2)rSiO(3-x) / 2(OR′)x)m, (HSiO(3-x) / 2(OR′)x)n′(MeSiO(3-x) / 2(OR′)x)o′(RSiO(3-x) / 2(OR′)x)p, (R1SiO(3-x) / 2(OR′)x)q where Ph is a phenyl group, Me is a methyl group; R′ is hydrogen atom or a hydrocarbon group having from 1 to 4 carbon atoms; R is selected from an aryl sulfonate ester group; and R1 is selected from substituted phenyl groups, ester groups, polyether groups; mercapto groups, and reactive or curable organic functional groups; and r has a value of 0, 1, 2, 3, or 4; x has a value of 0, 1 or 2; wherein in the resin m has a value of 0 to 0.95; n has a value of 0.05 to 0.95; o has a value of 0.05 to 0.95; p has a value of 0.05 to 0.5; q has a value of 0 to 0.5; and m+n+o+p+q=1.

Disclosed are processes for preparing modifiable poly(aralkyl ketone)s having active methylene group(s) in the main chain comprising reacting an aralkanoic acid or mixtures thereof in the presence of one alkane or aryl sulfonic acid and a condensing agent. Also disclosed are novel modifiable poly(aralkyl ketone)s obtainable by the processes of the inventions.

An excellent EL device having low driving voltage, high luminous efficiency and long life can be obtained by using a charge-transporting thin film composed of a charge-transporting varnish which contains an arylsulfonic acid compound represented by the formula (1) or (2) below as an electron-acceptor material especially in an OLED device or a PLED device.[In the formulae, X represents O, S or NH; A represents a naphthalene ring or anthracene ring having a substituent other than X and n SO3H groups; B represents a substituted or unsubstituted hydrocarbon group, 1,3,5-triazine group or a substituted of unsubstituted group represented by the following formula (3) or (4):(wherein W1 and W2 each independently represents O, S, an S(O) group, an S(O2) group, or a substituted or unsubstituted N, Si, P or P(O) group); n indicates the number of sulfonic acid groups bonded to A which is an integer satisfying 1≦n≦4; q indicates the number of B—X bonds which is an integer satisfying 1≦q; and r indicates the number of recurring units which is an integer satisfying 1≦r.].

A process for preparing an alkyl aryl sulphonic acid comprising the steps of:(a) contacting an alkyl aromatic hydrocarbon with a gaseous sulphonating agent to produce (i) a first liquid reaction product comprising an alkyl aryl sulphonic acid and (ii) a gaseous effluent stream;(b) separating the first liquid reaction product from the gaseous effluent stream;(c) purifying the gaseous effluent stream to provide a cleaned gaseous stream and a second liquid reaction product;(d) recycling the second liquid reaction product to the first liquid reaction product produced after separation step (b) to produce a third liquid reaction product comprising alkyl aryl sulphonic acid;wherein the alkyl aromatic hydrocarbon is obtained by contacting an aromatic hydrocarbon with an olefin under alkylating conditions, and wherein said olefin is obtained by dehydrogenation of a Fischer-Tropsch derived paraffinic feedstock.

An organic acid composition for use in oil industry activities, said composition comprising an arylsulfonic acid in water as well as the use of said composition to perform various operations in the oil industry. There is also disclosed a solid acid composition comprising a corrosion inhibitor ready for dissolution and use.

A composition comprising a stable mixture of at least one stain resist agent, at least one soil resist agent, and at least one coapplication enhancer, the enhancer comprising at least one of an alkali metal salt; alkali metal aryl salt; ammonium salt; ammonium aryl salt; aryl sulfonic acid; urea; amide; alkylamide; dialkylamide; amide of C1 to C6 alkanoic acids or of C2 to C6 alkandioic acids; diamides of C2 to C6 alkandioic acids; cyclic imide of C2 to C6 alkandioic acids; C3 to C6 lactams, or combinations thereof, is disclosed.

The present invention relates to preparation process of hydrothermally catalytic cracking viscosity reducer containing amphiphilic structure for thick oil exploitation. The preparation process includes the following steps: 1. preparing material arylsulfonic acid in 19-21 weigh portions, and iron oxide powder in 1.8 or 1.2 weigh portions; and 2. reaction between arylsulfonic acid and iron oxide powder at 80-160 deg.c for 1-3 hr, dissolving the resultant with acetone in 0.9-1.3 times arylsulfonic acid weight, filtering and stoving the filtrate in a stove at 50-80 deg.c to obtain the brown ropy liquid viscosity reducer. The present invention has the features of low cost, high universality and good low temperature viscosity reducing effect.

Some aryl sulfonic acid-functionalized solids were prepared by a new method. The catalytic activities of esterification by the prepared aryl sulfonic acid-functionalized solids were also tested.