Abstract: A process for the production of acrylic fibers, in particular a spinning process for obtaining precursor fibers of carbon fiber by the wet spinning of a polymer solution in an organic solvent and the relative apparatus.

Abstract: An integrated and improved, single-step, process for the production of a carbon fiber precursor is described, specifically a process which starts from the comonomers and reaches the spinning step, obtaining the final precursor fiber.

Abstract: A process for the recovery and recycling of unreacted monomer in a one-step process for the production of a carbon-fiber precursor. An integrated and improved single-step process for the production of a carbon-fiber precursor is also described, which starts from the co-monomers and reaches the spinning step obtaining the final precursor fiber, which provides for the recovery of the unreacted monomers at the end of the polymerization step and their recycling to the polymerization process itself.

Abstract: A process for the production of acrylic fibers, in particular a spinning process for obtaining precursor fibers of carbon fiber by the wet spinning of a polymer solution in an organic solvent and the relative apparatus.

Abstract: An integrated and improved, single-step, process for the production of a carbon fiber precursor is described, specifically a process which starts from the comonomers and reaches the spinning step, obtaining the final precursor fiber.

Abstract: An integrated and improved process for the production of acrylic fibers is described, specifically a process that starts from the comonomers and reaches the spinning step obtaining the final fiber.

Abstract: An optimized process for the preparation of a spinning solution for the production of acrylic fiber precursors (PAN) of carbon fibers and an optimized process for the production of carbon fibers from said acrylic precursor (PAN), are described.

Abstract: An optimized process for the preparation of a spinning solution for the production of acrylic fiber precursors (PAN) of carbon fibers and an optimized process for the production of carbon fibers from said acrylic precursor (PAN), are described.

Abstract: A process for the preparation of a homogeneous spinning solution for the production of acrylic fibers, which includes: preparing an aqueous suspension of homopolymer or copolymer of acrylonitrile through the polymerization of monomers in aqueous suspension, removal of the unreacted monomers, filtration and washing of the aqueous suspension, obtaining a filtration cake; dispersing the filtration cake; and evaporating the dispersion of polymer or obtaining the homogeneous spinning solution.

Abstract: A process is described for the preparation of a homogeneous spinning solution for the production of acrylic fibers, which comprises i) a preparation step of an aqueous suspension of homopolymer or copolymer of acrylonitrile through the polymerization of monomers in aqueous suspension, removal of the unreacted monomers, filtration and washing of the aqueous suspension, obtaining a filtration cake, ii) a step for dispersing the filtration cake and a step iii) for evaporating the dispersion of polymer or obtaining the homogeneous spinning solution.

Abstract: A process is described for the preparation of a homogeneous spinning solution for the production of acrylic or modacrylic fibers which comprises the following steps: i) preparation of an intimate mixture of a homopolymer or copolymer of acrylonitrile in powder form with a solid solvent in powder form, at a temperature lower than the melting point of the solid solvent; ii) gradually heating the intimate mixture of solids coming from step i) to a temperature ranging from 70° C. to 150° C. in a time ranging from 0.5 to 30 minutes, until the complete dissolution of the homopolymer or copolymer in the solvent and the formation of a homogeneous spinning solution. Said spinning solution is then fed to a storage tank or to the spinning line.

Abstract: A process for the preparation of a homogeneous spinning solution for the production of acrylic fibers comprising: i) preparation of a homogeneous suspension by mixing a powder homopolymer or copolymer of acrylonitrile with a mixture of DMSO/water ranging from 94.5/5.5 to 97/3% w/w at a temperature ranging from 5° C. to 10° C., said mixing being carried out in a time from 5 to 30 minutes, by spraying a stream of the DMSO/water solvent onto a stream of powder homopolymer or copolymer of acrylonitrile, disgregated and premixed; ii) heating the homogeneous suspension from step i) to a temperature from 70° C. to 150° C. in a time from 0.5 to 30 minutes, until the complete dissolution of the homopolymer or copolymer and the formation of a homogeneous solution. This spinning solution is then fed to a storage tank or to the spinning line.

Abstract: A process is described for the preparation of a homogeneous spinning solution for the production of acrylic fibers which comprises the following steps: i) preparation of a homogeneous suspension by mixing a powder homopolymer or copolymer of acrylonitrile with a mixture of DMSO/water ranging from 94.5/5.5 to 97/3% w/w at a temperature ranging from 5° C. to 10° C., preferably a mixture of DMSO/water 95/5 at a temperature of 5° C., said mixing being carried out in a time ranging from 5 to 30 minutes, by spraying a stream of the DMSO/water solvent onto a stream of powder homopolymer or copolymer of acrylonitrile, disgregated and premixed; ii) heating the homogeneous suspension coming from step i) to a temperature ranging from 70° C. to 150° C. in a time ranging of from 0.5 to 30 minutes, until the complete dissolution of the homopolymer or copolymer and the formation of a homogeneous solution. This spinning solution is then fed to a storage tank or to the spinning line.

Abstract: Polyaminoacid builders or co-builders having the general formula: ##STR1## that are useful in the formulations of detergents are disclosed. Preferred detergent formulations contain from 5 to 50 percent by weight of the polyaminoacid builder, preferably polyaspartic aicd or polyglutamic acid, together with surface-active agents, aluminosilicates and other detergent additives.

Abstract: The invention relates to modified materials based on polyacrylonitrile having amidic groups on their surface. The modification gives the material greater hydrophilic characteristics improving its comfort properties. In addition, it permits the polyacrylonitrile to be dyed also with acidic dyes thus making it possible for it to be used for the preparation of yarns mixed with natural fibres, such as wool for example. The process for their production involves treatment of the material with enzymes of the nitrile hydratasis class obtained from Brevibacterium imperiale.

Abstract: 4-substituted anthracyclinones of formula (I): ##STR1## wherein R represents a straight or branched alkyl, alkenyl or alkynyl group of up to 16 carbon atoms optionally substituted by (a) an aryl group which is unsubstituted or substituted by an inert group such as an alkyl, alkoxy or nitro group; (b) an alkoxy group; (c) a trialkylsilyl group, (d) an ester group or (e) an amido group, are intermediates in the preparation of antitumor anthracycline glycosides of formula (IX): ##STR2## wherein R is as defined above and R.sub.1 is a hydrogen atom or a hydroxy group, and pharmaceutically acceptable salts thereof.

Abstract: An in vitro process for preparing 6((1R)-hydroxyethyl) penem acids by hydrolyzing the carboxylic ester derivative thereof using an enzyme capable of selectively hydrolyzing the ester group at the 3-position of the carboxylic acid ester using an esterase, acylase or lipase enzyme, wherein the enzymatic hydrolysis is effected at a pH in the range of from 5 to 8 and at a temperature in the range of 20.degree. C. to 40.degree. C.

Abstract: A cobalt based catalyst, and the method for preparing it, are disclosed. The catalyst is obtained from the reaction between NaCo(CO).sub.4 and s-trichloro triazine and is advantageously used in the processes of carbonylation of naphthalene mono- and disulfonates in order to yield naphthalene esters and acids.

Abstract: This invention relates to use of polyaminoacids as builders or co-builders in the formulation of detergents. These polyaminoacids, which are highly efficient as complexing agents, have good resistance to heat and stability to pH and are entirely biodegradable, have been chosen among those having the general formula: ##STR1## with substituents which are defined in the following description. The formulations of detergents contain, apart from the above builders, surface active agents, alumina-silicates and additives chosen from neutral salts, enzymes, bleaching agents, stabilizers, anti-foaming agents, perfumes, bactericides.

Abstract: A biotechnological process for preparing L(-)-carnitine chloride, having the formula ##STR1## comprising: (a) reacting a racemic ester of (R,S)-3,4-epoxybutyric acid having the formula ##STR2## wherein R is an alkyl group having from 1 to 10 carbons or a benzyl group, with an enzyme capable of selectively hydrolyzing enantiomer S(-);(b) separating the enantiomer S(-) from non-reacted ester which is present in predominantly the R(+) form;(c) reacting the non-reacted ester obtained in step (b) with an enzyme capable of quantitatively hydrolyzing the R(+) form to obtain thereby a salt of 3,4-epoxybutyric acid in the R(+) form having the formula ##STR3## wherein X is Na, K, or Li; (d) reacting the salt obtained in step (c) with a molar excess of trimethylamine; and(e) treating the reaction product of step (d) with HCl to remove excess trimethylamine and to obtain thereby the L(-)-carnitine chloride of formula (I).