Abstract: A liqid composition polymerizable under the influence of free-radical initiators to yield crosslinked polymers useful as organic glasses endowed with high abrasion strength, contains an oligomer allyl-carbonate with two end allyl groups, a monomer allyl-carbonate with at least four end allyl groups and possibly also one or more reactive diluents containing groups of allyl, vinyl or methacryl type.

Abstract: The invention discloses a catalyst on the basis of silicon and titanium having the form of microspheres and constituted by oligomeric silica and by titanium-silicalite crystals having an oligomeric silica/titanium-silicalite molar ratio comprised within the range of from 0.05 to 0.11, wherein the crystals of titanium-silicalite are encaged by means of Si-O-Si bridges.

Abstract: A mixture of linear and branched-chain detergent oxo-alcohols, containing from 11 to 16 carbon atoms in the molecule, is dissolved in a hydrocarbon or ether solvent, and the solution thus obtained is cooled to obtain a dispersion of a solid phase in a liquid phase.The solid phase constituting the linear-chain oxo-alcohol fraction is separated and recovered. The branched-chain oxo-alcohol fraction is separated and recovered from the liquid phase.

Abstract: Process for the production of N-methylcarbamates: ##STR1## (wherein RO- is the radical of a substituted phenol or of a naphthol), wherein:in a first reaction step methylamine and diphenyl carbonate are reacted with each other, operating in the liquid phase and as a continuous process, in order to form phenol and phenyl-N-methylurethane;in a second reaction step phenyl-N-methylurethane, within the related reaction mixture outcoming from the first step, is thermally continuously decomposed, to yield a gaseous stream containing methyl isocyanate, from which the components different than methyl isocyanate are condensed off;in a third step the methyl isocyanate stream, outcoming from the second step, after an optional preliminary condensation, is continuously fed and contacted with a solution of a substituted phenol or of a naphthol in an inert organic solvent, containing a basic catalyst, to form N-methylcarbamate (I);N-methylcarbamate (I) is finally recovered from the reaction mixture outcoming from the third st

Abstract: The application relates to a process for synthesizing carbonic allyl esters from polyhydric alcohols, which are reacted with diallyl carbonate in the presence of a basic catalyst, which can be chosen from sodium hydroxide, sodium carbonate, sodium alcoholate, organic bases or basic ion exchange resins.The final products obtained differ according to the ratio of the components of the starting mixture. Thus, in the case of diols with a diallyl carbonate/diol ratio greater than or equal to 10, the resultant product is constituted by the bis allyl carbonate of the diol together with a quantity of less than or equal to 10% of oligomers represented mainly by dimers. If the ratio is less than 10, the percentage of oligomers rises until, in the case of an approximately stoichiometric ratio, it reaches a value close to 70% of the reaction product.

Abstract: A composition based on aliphatic polycarbonates containing urethan groups and acrylic or metacrylic end groups, to be cross-linked in the presence of radicalic initiators for their functionalization with acrylic or metacrylic groups of a mixture composed of diols, polyols and their oligomeric derivatives terminated by OH groups and containing in their molecule carbonate groups and urethan groups.

Abstract: A polymerizable liquid composition is disclosed, intended for preparing polymerizates having outstanding optical and physical properties, said composition consisting of a bis (allylcarbonate) of a dihydric alcohol oligomer, a bis (allylcarbonate) monomer of a dihydric or a trihydric alcohol, or an allyl ester, or a triallyl cyanurate or isocyanurate, and an acrylic or vinylic monomer, said composition being polymerized in bulk with the aid of at least one radicalic initiator. Highly transparent articles are obtained, which are very useful for fine optical applications.

Abstract: Process for the production of alkyl isocyanates which can be defined by the general formula: R--N.dbd.C.dbd.O wherein R is an alkyl radical having from 1 to 4 carbon atoms by thermal decomposition of phenyl-N-alkyl urethans which can be defined by the general formula: ##STR1## wherein R has the above defined meaning. Said thermal decomposition is carried out without any substance having a catalytic activity being present in the decomposition reaction, by heating to a temperature of from 180.degree. C. to 210.degree. C. under the atmospherical pressure or a slightly reduced pressure, a mixture of phenol and phenyl-N-alkyl urethan, in a molar ratio of the former to the latter equal to or nearly equal to 1:1, removing by vaporization the phenol and the alkyl isocyanate from said vaporized products and maintaining in the reaction mixture, substantially throughout the thermal decomposition a molar ratio of phenol to phenyl-N-alkyl urethan not lower than about 1:1.

Abstract: The application relates to a process for synthesizing unsaturated carbonic acid esters from polyhydric alcohols, which are reacted with alkyl carbonates and unsaturated alcohols in the presence of a basic catalyst, which can be chosen from sodium hydroxide, sodium carbonate, sodium alcoholate, organic bases and basic ion exchange resins.

Abstract: The application relates to a process for synthesizing carbonic allyl esters from polyhydric alcohols, which are reacted with diallyl carbonate in the presence of a basic catalyst, which can be chosen from sodium hydroxide, sodium carbonate, sodium alcoholate, organic bases or basic ion exchange resins.The final products obtained differ according to the ratio of the components of the starting mixture. Thus, in the case of diols with a diallyl carbonate/diol ratio greater than or equal to 10, the resultant product is constituted by the bis allyl carbonate of the diol together with a quantity of less than or equal to 10% of oligomers represented mainly by dimers. If the ratio is less than 10, the percentage of oligomers rises until, in the case of an approximately stoichiometric ratio, it reaches a value close to 70% of the reaction product.

Abstract: A method for preparing monoalkylethers of hydroquinone and of substituted hydroquinones of general formula ##STR1## in which R is an alkyl group and R.sub.1 is hydrogen or an alkyl group, wherein a hydroquinone compound of general formula ##STR2## is reacted with an alcohol or formula R-OH in the presence of transition metal salts, either in the presence or in the absence of air or oxygen.

Abstract: A process for the preparation of aromatic urethans by reaction between aromatic amines and alkyl carbonates, said reaction being carried out in the presence of a catalyst composed of an alcoholate of an alkali metal or an alkaline earth metal. The reaction is caused to take place at a temperature which is variable from +50.degree. C. and +150.degree. C., in the liquid phase and with a molar ratio of the carbonate to the amine of from 10:1 to 1:10.

Abstract: A method is disclosed for obtaining high-purity ethylene glycols in which the improvement consists in reducing the oxygen-containing organic impurities by treating their aqueous solutions as obtained during the processing of ethylene oxide with a solution of an alkali metal borohydride, sodium borohydride being preferred.A definitely alkaline environment is preferred. Ethylene glycols can thus be obtained which are particularly suitable for use in the fibre-manufacturing industry. Such glycols have extremely low UV-absorbance values.

Abstract: Aromatic alkylamines are prepared by reacting an amine with an alkyl ester of carbonic acid in the presence of an organic iodide, at a temperature below 150.degree. C.

Abstract: A process for preparing dimethylcarbonate by reacting methanol with mixtures of carbon monoxide and oxygen which also contain hydrogen. The catalyst is constituted by a salt of a metal of groups IB, IIB or VIII of the periodic system, dissolved or dispersed in the reaction medium.It has been found that the hydrogen does not interfere in the reaction, so that a hydrogen-enriched gaseous mixture (synthesis gas) is withdrawn from the reactor. It is therefore particularly advantageous in that it produces dimethylcarbonate and at the same time provides hydrogen-enriched synthesis gas.

Abstract: A process for the preparation of alkylene glycols starting from the corresponding alkylene oxide, which is reacted with water in the presence of carbon dioxide, wherein the reaction catalyst is selected amongst the organic bases, preferably a tertiary amine, whereby the conversion rate and the selectivity are improved.

Abstract: Phenolic ethers are prepared starting from phenol or a phenolic derivative and an alkyl carbonate which are reacted at a comparatively low temperature (below 160.degree. C.) and with good yield and selectivity by using a catalytic system composed by a base, preferably a tertiary amine, and by an iodide, either organic or inorganic.

Abstract: A method for the preparation of organic esters of oxalic acid by reaction of carbon monoxide under pressure with the corresponding alcohol is disclosed, the improvement consisting in the use of a quite particular catalyst system. The catalyst is a binary system in which the principal member is a palladium complex and the co-catalyst is a compound, preferably an organic compound having an acidic nature, no matter how weak.

Abstract: Carbonic acid esters are prepared by reacting the alcohol concerned with oxygen and carbon monoxide in the presence of a catalyst which is a salt of a metal belonging to the Groups IB, IIB and VIII of the Periodic Table: the least possible number of inorganic anions is desirable in order to reduce the acidity of the environment as far as possible. The salts of monovalent copper are preferred and high yields and selectivities are obtained.

Abstract: An aromatic carbonate having the formula: ##STR1## wherein R' is alkyl and R is alkyl, alkoxy, aryl, aryloxy or NO.sub.2, is prepared by reacting the related phenol or an acyl ester thereof with an alkyl, cyclic or aryl-alkyl carbonate in the presence of a catalyst such as AlCl.sub.3.