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Enichem Synthesis S.p.A. Patents
Assignee:
Enichem Synthesis S.p.A.
Address:
Palermo, IT
No. of patents:
102
Patents:


1 2 3


Patent Number Title Of Patent Date Issued
6642172 Extruded catalyst based on silica/alumina gel November 4, 2003
A catalyst in the form of extruded bodies is disclosed, which consists of an inert binding agent and a catalytically active phase of a silica/alumina gel. The catalyst is particularly active in acid-catalysed reactions.
6180011 Method for removing hydrocarbon products from water surfaces January 30, 2001
A method for removing hydrocarbon products from water surfaces, which entails contacting the hydrocarbon products with a crystalline polypropylene, which when observed under a microscope of 2500 magnetization, exhibits a spongy surface having relatively homogeneous intercommunicating
6084143 Catalytic composition and process for the alkylation or transalkylation of aromatic compounds July 4, 2000
A catalytic composition is described for the alkylation or transalkylation of aromatic compounds consisting of zeolite Beta, as such or modified by the isomorphic substitution of aluminium with boron, iron or gallium or by the introduction of alkaline/earth-alkaline metals following ion
5888471 Synthetic crystalline porous material containing oxides of silicon, titanium and gallium March 30, 1999
A synthetic, crystalline, porous material is disclosed, together with the related preparation process. Such material of zeolitic nature containing oxides of silicon, titanium and gallium corresponds, in the calcined and anhydrous state, to the following empyrical formula:wherein p has a
5888466 Process for preparing amorphous, catalytically active silicoaluminas March 30, 1999
An amorphous, micro/mesoporous silica-alumina gel with controlled pore size, having a surface area of at least 500 m.sup.2 /g and with a molar ratio of SiO.sub.2 :Al.sub.2 O.sub.3 of at least 30:1, is prepared by hydrolysing and causing a tetra-alkyl ammonium hydroxide, an aluminum t
5811612 Catalytic composition and process for the alkylation or transalkylation of aromatic compounds September 22, 1998
A catalytic composition is described for the alkylation or transalkylation of aromatic compounds consisting of zeolite Beta, as such or modified by the isomorphic substitution of aluminium with boron, iron or gallium or by the introduction of alkaline/earth-alkaline metals following ion
5730908 Photochromatic and thermochromatic compounds and their application in polymeric materials March 24, 1998
A description follows of photochromatic and thermochromatic compounds, belonging to the group of spiro-indoline-oxazines, and their application in polymeric materials.
5686644 Procedure for the production of alkyl carbonates November 11, 1997
Dialkyl carbonate is prepared by reacting an alcohol with a gaseous mixture of carbon monoxide and oxygen in the presence of cuprous chloride as catalyst and hydrochloric acid as in situ regenerator of the catalyst.
5685957 Method for removing acidic and salt impurities from an aqueous condensed phase containing dimeth November 11, 1997
Acidic and salt impurities are removed from a condensed phase obtained from dimethyl carbonate synthesis by obtaining the condensed phase from the effluent of a reactor in which carbon monoxide, oxygen and methanol are reacted to form dimethyl carbonate, the condensed phase containing ac
5672799 Process for the preparation of cumene September 30, 1997
Process for the preparation of cumene by the alkylation of benzene with propylene, catalyzed by zeolite Beta into which certain quantities of suitable alkaline, alkaline-earth or metallic cations have been introduced by ion exchange.
5631395 Method for removing the acidic impurities contained in a vapourized stream composed by organic v May 20, 1997
Method for removing the acidic impurities contained in a vaporized stream consisting of an alkanol, an alkyl carbonate, water and still other organic species in minor amounts, which method consists in sending said stream to a solid adsorption reactor comprising alumina or activated c
5625108 Process for preparing amorphous, catalytically active silicoaluminas April 29, 1997
An amorphous, micro/mesoporous silica-alumina gel with controlled pore size, having a surface area of at least 500 m.sup.2 /g and with a molar ratio of SiO.sub.2 :Al.sub.2 O.sub.3 of at least 30:1, is prepared by hydrolysing and causing a tetra-alkyl ammonium hydroxide, an aluminum t
5602212 Linear copolyester containing phosphorous, procedure for its preparation and its use as a flame- February 11, 1997
A linear copolyester is prepared by polycondensation of an aromatic bicarboxylic acid with an alkylene glycol and with a carboxyphosphinic acid or anhydride which produces monomeric units having the formula: ##STR1## wherein R.sub.1 is an alkylene or phenyl radical and R.sub.2 is an
5599876 Composition and procedure for the preparation of organic glasses February 4, 1997
A polymerizable liquid composition includesa polymerizable poly(allyl carbonate) of an aliphatic or cyclo-aliphatic polyol;an organic peroxide generator of free radicals selected from the group of perketals, and possiblyan organic dye and/or an organic photochromic compound.The compositions
5580916 Vulcanizable compositions of nitrile rubbers December 3, 1996
A description follows of vulcanizable compositions of nitrile rubbers containing a plasticizer, a vulcanizing agent and normal additives, wherein the plasticizer is an organic carbonate selected from those which can be defined with the formula (I): ##STR1## or with the formula (I
5550207 Linear copolyester containing phosphorous, procedure for its preparation and its use as a flame- August 27, 1996
A linear copolyester is prepared by polycondensation of an aromatic bicarboxylic acid with an alkylene glycol and with a carboxyphosphinic acid or anhydride which produces monomeric units having the formula: ##STR1## wherein R.sub.1 is an alkylene or phenyl radical and R.sub.2 is an
5536864 Process for producing dimethyl carbonate and apparatus suitable for such purpose July 16, 1996
The reaction between methanol, carbon monoxide and oxygen for preparing dimethyl carbonate, in the presence of cuprous chloride as the catalyst, is carried out in a special reactor constituted by two parallel, vertical tubes, at the base of one of which the fresh gas and the recycle gas
5527943 Method for removing acid and saline contaminants from a gaseous stream leaving a dimethylcarbona June 18, 1996
A method is described enabling HCl and possible entrained CuCl particulate to be removed from a gas-vapor stream leaving a dimethylcarbonate synthesis reactor. The contaminant removal is effected by one of the process fluids used in a small quantity.
5514254 Procedure for the photochlorination of alkyl-aromatic compounds May 7, 1996
An alkyl-aromatic compound is selectively photochlorinated in the side chain in a cyclic reaction system wherein said compound is continuously circulated between a container and photochlorination reactor.The compound is partially chlorinated after each passage through the photochlorinati
5505869 Low smoke lubricating composition for two-phase engines April 9, 1996
A carbonate ester of an aliphatic triol or tetraol which can be defined with the following formula: ##STR1## wherein R.sub.1, R.sub.2, R' and p are as defined in the description, is used as a lubricating base with a low quantity of smoke for two-phase engines with internal combus
5498811 Process for producing gasolines and jet fuel from n-butane March 12, 1996
Polymeric fuels are produced from saturated C.sub.4 hydrocarbons by a process comprising:(A) dehydroisomerizing a gas mixture comprising predominantly of n-butane and hydrogen in a catalytic reactor containing a catalyst (a) of platinum supported on alumina, whose surface is coated with
5489316 Process for making industrial organic solvents and hydrocarbons used as fuels February 6, 1996
Process for marking industrial organic solvents miscible with water and petroleum products gaseous at atmospheric pressure and room temperature and liquid when compressed at low pressure, by the addition to the above solvents of a primary nitroderivative having the general formula
5462984 Solid blends of stabilizers for polymers October 31, 1995
Solid stabilizers for polymers comprises a blend of (a) organic polymer and (b) at least one silicon-containing compound having a sterically hindered amine group in the molecule in quantities of between 40% and 50% by weight of the final solid blend.
5457213 Catalytic procedure for the preparation of organic carbonates October 10, 1995
Catalytic procedure for the preparation of an organic carbonate having general formula (I): ##STR1## wherein R represents a C.sub.1 -C.sub.10 alkyl radical, linear or branched, or a C.sub.5 -C.sub.8 cycloalkyl radical; or of a cyclic organic carbonate having general formula (II):
5457037 Cloning of the gene coding the isoamylase enzyme and its use in the production of said enzyme October 10, 1995
The structural gene encoding isoamylase from Pseudomonas SMP 1 is obtained. Also described are vectors comprising the isoamylase gene and host microorganisms transformed by these vectors. The transformed host microorganisms are capable of expressing and/or secreting mature isoamylase
5447991 Flame-resistant polyolefinic fibres and films September 5, 1995
Polyolefinic fibres and films are made flame-resistant by the addition of a flame-resistant additive made up of a copolyester containing units deriving from: a) terephthalic acid; b) alkylenic glycol (C.sub.2 --C.sub.6) ; and c) phenyl hydroxymethylene phosphinic acid.These fibres and fi
5423994 Ski lubricant comprising a hydrocarbon compound containing a perfluoro segment June 13, 1995
Compounds which can be defined by the formula (I):wherein:n is a numeral comprised within the range of from 1 to 21;m is a numeral comprised within the range of from 3 to 25;n+m is a numeral equal to, or higher than, 18;with the chain of carbon atoms being either linear or branchedare used as agents
5395949 Process and catalyst for preparing organic carbonates March 7, 1995
Organic carbonates and cyclic organic carbonates are prepared by reacting an aliphatic or cycloaliphatic alcohol, or, respectively, an aliphatic diol, with carbon monoxide and oxygen, by operating in the presence of a complex catalyst of cobalt with organic ligands bearing one or more ox
5366991 Pyrazolecarboxamides exhibiting insecticide and acaricide activity November 22, 1994
5-pyrazolecarboxylic acid amide-based insecticide and acaricide compounds of general formula (I): ##STR1## in which: R.sub.1 represents a hydrogen atom, a linear or branched C.sub.1 -C.sub.4 alkyl group or a benzyl group;R.sub.2 represents a hydrogen atom or a linear or branched C.su
5357002 Polymer containing chelating groups, process for preparing it and its use in water purification October 18, 1994
Water insoluble polymers containing hydrophilic pendant moieties ending with a chelating group are disclosed. The polymers are useful in the purification of water polluted by heavy metals such as mercury and lead. The polymers have the general formula P--(--(--O--R).sub.n --(NH--Q).sub.p
5354454 Continuous process for deasphalting and demetallating a residue from crude oil distillation October 11, 1994
A continuous process for deasphalting and demetallating a residue from crude oil distillation, by means of dimethyl carbonate as extraction solvent, comprises:mixing a residue from crude oil distillation with a recycled liquid stream containing oil and dimethyl carbonate, in order to pro
5350786 Process of (co)polymerization of .alpha.-olefins in the presence of stabilizers September 27, 1994
Stabilizers for organic polymers, consisting of one or more compounds of the classis of the sterically hindered amines (HALS) are directly added to the reaction mixture during the (co)polymerization of the .alpha.-olefins or of their mixtures with other unsaturated monomers.The so-obtain
5338787 New pentaerythryl phosphonates containing self-extinguishing thermoplastic compositions August 16, 1994
A new group of pentaerythryl diphosphonates and poly(pentaerythryl diphosphonates) are described. Flame-retardant compositions are also described, which include a thermoplastic polymer and a certain amount of self-extinguishing agent consisting of one of the above-mentioned pentaeryt
5326818 Polysiloxanic stabilizers containing sterically hindered phenol groups and reactive groups July 5, 1994
Polymeric stabilizers with a polysiloxanic structure contain sterically hindered phenol groups and reactive groups capable of binding themselves to the polymeric structure to be stabilized. These polymeric stabilizers are particularly suitable for applications which require the non-e
5322958 Catalytic procedure for the preparation of organic carbonates June 21, 1994
Catalytic procedure in gas phase for the preparation of a symmetrical or asymmetrical organic carbonate having the general formula (I): ##STR1## wherein R and R', the same or different, represent a C.sub.1 -C.sub.4 alkyl radical, linear or branched, which includes reacting at least o
5315034 Procedure for the preparation of alkyl isocyanates May 24, 1994
Multistep process for the preparation of alkyl mono and diisocyanates consisting in reacting the corresponding aliphatic amine or diamine with dimethylcarbonate and, substantially, in partially vaporizing and converting the urethane thus formed in an evaporator to subsequently termin
5310841 Liquid composition polymerizable to yield organic glasses with low water absorption and high the May 10, 1994
A liquid composition, polymerizable by free-radical polymerization to yield organic glasses which are endowed with characteristics of low water absorption and high thermal stability, is constituted by the product of transesterification of diallyl-carbonate with a cycloaliphatic diol or a
5302735 Polysiloxanic stabilizers containing sterically hindered phenol groups and oxamidic groups April 12, 1994
Polysiloxanic compounds, containing sterically hindered phenol groups and oxamidic groups in the molecule, obtained by the copolymerization of monomers having general formula (I):with monomers having general formula (II): ##STR1##
5296521 Fast-crystallizing polyester compositions March 22, 1994
The present invention relates to fast-crystallizing polyester compositions comprising: (a) a thermoplastic polyester resin; (b) a nucleating agent of the formula: ##STR1## wherein: R is an alkali or alkaline-earth metal; m is 1, 2 or 3; n takes an average value within the range o
5290533 Method for production of a coated substrate with controlled surface characteristics March 1, 1994
A crystalline, porous, synthetic material is disclosed, together with its related preparation process.Such a material of zeolitic character, containing silicon, titanium and iron oxides, corresponds, in its calcined and anhydrous state, to the following empi rical formulawherein p has a
5288869 Pentaerythryl phosphonates and their use in self-extinguishing thermoplastic polymeric compositi February 22, 1994
A new group of pentaerythryl diphosphonates and poly(pentaerythryl diphosphonates) are described. Flame-retardant compositions are also described, which include a thermoplastic polymer and a certain amount of self-extinguishing agent consisting of one of the above-mentioned pentaeryt
5288839 Diol-terminated polycarbonates February 22, 1994
Diol-polycarbonates having the general formulawhere R.sub.1, R.sub.2, R.sub.3, X and Y have the meaning specified in the text, are used in the synthesis of prepolymers which in turn can be used in reactive adhesive and/or sealing formulations of the hygro-, photo- or thermosetting type,
5286816 Organic glass with improved impact strength and with a refractive index equal or similar to that February 15, 1994
An organic glass with improved impact strength and with a refractive index equal or similar to that of mineral glass (crown glass), is composed of the product of the radicalic polymerization of the polymerizable liquid composition obtained by the transesterification of:(A) diallyl carbon
5280051 Composition for the production of artificial marble or granite January 18, 1994
Artificial marble or granite having excellent aesthetic properties, patterns and tonalities which cannot be found in natural materials are prepared from a composition containing a polymerizable poly(allyl carbonate) of a polyol and mineral filler, where the mineral filler is a carbon
5264604 Oxamidic stabilizers November 23, 1993
Oxamidic stabilizers containing organofunctional groups of silicon, capable of producing polymeric structures or of chemically binding themselves to a solid support.
5242624 Stabilizing mixture for compounds having a photochromatic activity September 7, 1993
Stabilizing mixture for photochromatic substances containing a cyclic amine chosen from 1,4-diazabicyclo-(2.2.2)octane and quinuclidine, or their derivatives, and at least one sterically hindered amine.
5241119 Process for the preparation of 4,4'-diaminodiphenyl-methane and its derivatives August 31, 1993
Process for the preparation of 4,4'-diaminodiphenylmethane and its derivatives.4,4'-diaminodiphenylmethane and its derivatives are prepared by the condensation of aniline, or its derivative, and aldehyde, or its precursor and/or isomerization of appropriate intermediate products. The rea
5240642 Process for obtaining granular forms of additives for organic polymers August 31, 1993
Process for obtaining granular forms of organic and inorganic antiacid additives and tetrakis-[3-(3,5-di-tert.-butyl-4-hydroxyphenyl)-propionyloxymethyl]-metha ne, carried out in the presence of an amount of the latter in the molten state, homogeneously distributed throughout the powd
5235062 Procedure for the preparation of bisoxazolidines containing urethanic groups August 10, 1993
New procedure for the preparation of polyoxazolidines which can be defined with the general formula: ##STR1## This procedure, which excludes the use of isocyanates, requires the simple transesterification of the dicarbamate of a diamine with an N-hydroxyalkyloxazolidine.
5234995 Method of crosslinking moisture curable systems with oxazolidinic silane and siloxanes August 10, 1993
New silanes containing at least two oxazolidinic moieties can be defined by means of the general formula: ##STR1## wherein X.sub.1, X.sub.2, X.sub.3 and X.sub.4 have the meaning as reported in the specification, and each one of A.sub.1, A.sub.2 and A.sub.3 represents from 0 to a
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