Abstract: The present invention is related to aqueous liquid detergent compositions comprising anionic esters of alkylpolygly-cosides and enzymes, and to the procedure for their preparation; the aqueous liquid detergent compositions of the invention exhibit long term enzymatic stability and excellent washing performance.

Abstract: Disclosed are paper coating formulations for rotogravure printing processes containing: a. 100 parts by weight or finely divided pigments; b. from 0.001 to 5 parts by weight of one or more substances selected from the group consisting of: mono-alkylsulfosuccinate; dialkylsulfosuccinates; sulfosuccinic acid mono-esters of ethoxylated and/or propoxylated fatty alcohols; sulfosuccinic acid di-esters of ethoxylated and/or propoxylated fatty alcohols; c. from 3 to 15 parts by weight of a polymeric acrylic binder, d. from 0.005 to 0.4 parts by weight of a dispersant.

Abstract: Disclosed is a process for cleaning wellbore walls, tubing or casings.

Abstract: Disclosed is a process for cleaning wellbore walls, tubing or casings.

Abstract: The process for the synthesis of an alkylpolyglucoside having the formula (I):H--(G).sub.n --O--R-- (I)whereinR is linear or branched, saturated or unsaturated C.sub.8 -C.sub.20 alkyl;G is a radical resulting from removal of a molecule of water from a monosaccharide; andn is an integer from 1 to 5;the process entailing reacting an alcohol with a monosaccharide or a compound capable of generating a monosaccharide in in situ, wherein the reaction is carried out in the presence of a catalyst consisting of one or more sterically hindered polyalkylarylsulfonic acids.

Abstract: An improved method for synthesizing alkylpolyglucosides comprising reacting a glycoside with a long-chain alcohol in the presence of a novel type of catalyst, constituted by an alkali or aryl sulfonic acid, wherein the sulfonic group is sterically hindered. Using these catalysts, a raw product is obtained which is practically free from byproducts. The resulting alkyl polyglucosides are completely biodegradable surfactants and can be used to formulate detergents.

Abstract: A process is disclosed for producing particular hydroxyalkyl glucosides in the presence of a binary catalyst.

Abstract: Process for the preparation of linear alkylbenzenes, wherein the benzene is reacted, in the presence of aluminum chloride or aluminum in powder form, with a mixture composed of C.sub.7 -C.sub.20 n-olefins and C.sub.7 -C.sub.20 chloroparaffins, with a molar ratio n-olefins/chloroparaffins between 70:30 and 99:1.

Abstract: This invention describes the preparation of a red pigment of iron oxide from ferrous salts, by simultaneous reduction of organic nitro derivatives.

Abstract: Aromatic amines and iron oxide pigment are produced by reacting a ferrous salt, a reduceable aromatic nitrogen compound chosen from nitroderivatives with a single nitro-group or with two nitro-groups and azoderivatives, and a basic compound, chosen from hydroxides and carbonates of ammonium, alkali metals and alkaline earth metals, operating at 25.degree.-200.degree. C. in an aqueous medium. The color of the pigment can be varied from yellow to black by increasing the reaction temperature and the molar ratio between ferrous salt and aromatic nitrogen compound.

Abstract: This invention describes a process for preparing a yellow iron hydroxide pigment from inorganic ferrous salts and aromatic nitro compounds.

Abstract: This invention describes a process for preparing a red iron oxide pigment from inorganic ferrous salts and aromatic nitro compounds.

Abstract: Hydrolysis of a titanyl sulphate solution is carried out according to the autonucleation method of gradually adding the solution to a body of water at a substantially constant rate over 10-20 minutes, in such a way as to obtain an ionic concentration after one minute of feeding of from 75 to 105 g/l, the concentration of sulphuric acid in the final hydrolysis solution being regulated to a value of from 310 to 330 g/l by adding water from the commencement of clouding of the hydrolysis solution up to the end of hydrolysis.

Abstract: Titanium sulphate solutions obtained in the sulphate process from titaniferous materials are hydrolized by contacting at 88.degree.-98.degree. C water with a first titanium sulphate solution having a TiO.sub.2 titer of 230-260 g/l and an acid factor of 1.75-1.85, adding at 88.degree.-98.degree. C to the mixture a second titanium sulphate solution having a TiO.sub.2 titer of 230-260 g/l and an acid factor of 2.1-2.4 and heating the resulting mixture at boiling point. A volumetric ratio of from 3:100 to 12:100 is maintained between the first and the second solution.