Enichem Synthesis S.p.a

Enichem Sintesi S.p.a.

Snamprogetti S.p.a.

Anic S.p.a.

Enichem S.p.a

Dow Corning Corporation

Montedison S.p.a.

Mapei Spa

Enichimica Secondaria, S.p.a.

Boston S.p.a.

Snamprogetti

Alberto Greco

Guglielmo Bertolini

Carlo Neri

Gabriele Lugli

Luigi Cassar

Sebastiano Cesca

Carlo Busetto

Mario Bruzzone

Margherita Corbellini

Mirko Osellame

Patrizia Blasioli

Enrico Pozzi

Franco Rivetti

Silvestro Costanzi

Luciano Pallini

Franco Mizia

Franco Pirinoli

Gino Dall'Asta

Sergio Giordano

Luigi Raisa

Gianfranco Pazienza

Omero Zavattini

Renato Butturini

Antonio Ausilio

Sergio Arrighetti

Maurizio Licchelli

Process for the preparation of fluid organosilicon compounds usable in adhesive, coating and sealant formulations is described. The process includes the synthesis of organosilicon prepolymer compositions starting from unsaturated polyurethanes obtained in turn from unsaturated monoalcohol polyethers and diisocyanates with a controlled NCO/OH ratio, to which chlorosilanes are added in the presence of methyl or ethyl orthoformates. These organosilicon compositions are able to cross-link through silicon-alkoxy end groups of the type:

Process for preparation of organosilicon compositions

The invention describes a process for the preparation of polycarbonate copolyester diols with a molecular weight ranging between 1000 and 6000 units having the following general formula: ##STR1## wherein the polycarbonate or polyether polycarbonate diol units ##STR2## represent a proportion of between 30 and 70% by weight of the whole polycarbonate or polyether carbonate co-polyester diol

Process for preparation of polycarbonate copolyester diols

A process is described for the preparation of polycarbonate polyether polyols characterized in that dimethylcarbonate (DMC) and one or more polyether diols are reacted at a ratio DMC/polyether diols of between 0.5 and 1.35, at a temperature of between 130.degree. and 175.degree. C. and in the presence of a catalyst consisting of an oxide, a carbonate or an alcoholate of a metal of the first or second group or a salt or organometallic compound of a metal belonging to the third or fourth or fifth group at a concentration of between 0.0001 and 0.01%.

Process for the preparation of polycarbonate copolyether polyols

A process for the preparation of polycarbonate copolyether diols comprising two successive reaction stages wherein in the first stage the precursor, bisdimethylcarbonate of polyether diols is synthesized by reacting, in a reactor equipped with a distillation column, one or more polyetherglycols with dimethyl carbonate, in the presence of a basic catalyst selected from the group consisting of an oxide, a hydroxide, a carbonate and an alcoholate of a metal belonging to the group of alkaline or earth-alkaline metals and in the second stage, the precursor, after being freed from the catalyst and excess dimethylcarbonate, is converted to polycarbonate copolyether diols by transesterification reaction with polyetherglycols in the presence of a solvent and an organometallic catalyst selected from compounds of tin, lead, titanium, zirconium and antimonium, said polycarbonate polyether diols having utility as additives in the field of polyurethane end-products, thermoelastomers, paints and adhesives.

Two-stage process for the preparation of polycarbonate copolyether diols

Diol-polycarbonates having the general formula

Diol-terminated polycarbonates

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 plurality of siloxane radicals

Method of crosslinking moisture curable systems with oxazolidinic silane

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.

Procedure for the preparation of bisoxazolidines containing urethanic

New polyoxazolidines can be defined with the general formula: ##STR1## where R, R.sub.1, R.sub.2 and n have the meaning specified in the description. These polyoxazolidines are useful cross-linking agents for hydrocuring systems based on polyisocyanates, acrylate polymers and polyepoxides, in compositions for paints, coatings, sealants and adhesives.

Polyoxazolidines with a structure containing carbonate groups, procedure

Copolyester-diol polycarbonates fluid at room temperature, having a number average molecular weight comprised within the range of from 1,500 to 6,000 with a glass transition temperature (T.sub.g) lower than -45.degree. C., useful in the sector of polyurethanes and in the sector of sealants, are obtained by means of a reaction of transesterification by starting from:

Copolyester-diol polycarbonates, process for producing them and their use

Silanes containing at least two oxazolidinic moieties

New polyoxazolidines can be defined by means of the general formula: ##STR1## wherein R, R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6 and n have the meaning as reported in the specification. These polyoxazolidines are useful as crosslinking agents for moisture-hardening systems on the basis of polyisocyanates, acrylate polymers and polyepoxides, in compositions for coatings, sealant compositions and adhesive compositions.

New polyoxazolidines, process for preparing them and use thereof

Novel silicon-organic compounds containing an oxazolidine group are defined by the general formula (I): ##STR1## wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, X, n and y have the meanings reported in the description. These compounds are capable of co-cross-linking and to act as adhesion promoters on various polar substrates, in compositions based on poly-isocyanates, polyepoxides or polacrylates, in the field of sealants and adhesives.

Novel silicon-organic compounds, containing an oxazolidine group

A reactive hot melt composition comprises the products of the reaction between (A) an aliphatic or aromatic diisocyanate and (B) a mixture containing: (1) a crystalline polycarbonate diol, (2) an elastomeric polycarbonate diol or an elastomeric polycarbonate copolyester diol, and possibly (3) a vitreous polycarbonate diol or a vitreous polycarbonate copolyester diol. The process for preparing the reactive hot melt composition is also described .

Reactive hot melt composition

Polyol-polycarbonates having a molecular weight comprising within the range from 750 to 2500, endowed with good rheologic characteristics and having a low glass transition temperature (Tg), are obtained by means of the reaction, under transesterification conditions, of

Polyol-polycarbonates and process for preparing them

Reactive stabilizing compounds, able to stabilize organic polymers, contain in their molecule a sterically hindered amino group and a hydrolyzable silyl function. In stabilizing organic polymers, said reactive stabilizing compounds can be hydrolyzed at the silyl function with the formation of silanol groups, which are made to interact in order to form complex resinous stabilizing structures. These latter are added in stabilizing quantities to the polymer to be stabilized. According to one particular embodiment, the hydrolysis at the silyl function and the formation of the resinous structure take place spontaneously within the polymer to be stabilized. According to a further embodiment, the reactive stabilizing compound is added to the polymer after being stably supported on a solid support by reaction with an inorganic solid having surface hydroxyl groups. According to a further embodiment, the reactive stabilizing compound is made to interact with the polymer so that the stabilizing compound becomes chemically bonded to the polymer chains. In all cases, stabilized polymers are obtained containing the stabilizing compound in a form which is not removable from the polymer. The processes for preparing the reactive stabilizing compounds and for preparing the stabilized polymer compositions are also described.

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Dresano, Italy

Alberto Greco