Abstract:
A process for the treatment of textile materials which comprises applying to the textile material an emulsion or suspension of one or more bleaching agents in a hydrocarbon or halogenated hydrocarbon solvent, substantially removing the solvent from the textile material, and subsequently washing the textile material, and an emulsion or suspension of a bleaching agent for use therein.
Abstract:
A fungal alpha-amylase is provided from Aspergillus fumigatus (AfAmyl). AfAmyl has an optimal pH of 3.5 and is operable at 30-75 degrees C., allowing the enzyme to be used in combination with a glucoamylase and an isoamylase in a saccharification reaction. This obviates the necessity of running a saccharification reaction as a batch process, where the pH and temperature must be readjusted for optimal use of the alpha-amylase or glucoamylase. AfAmyl also catalyzes the saccharification of starch substrates to an oligosaccharide composition significantly enriched in DP2 and (DPI+DP2) compared to the products of saccharification catalyzed by an alpha-amylase from Aspergillus kawachii. This facilitates the utilization of the oligosaccharide composition by a fermenting organism in a simultaneous saccharification and fermentation process, for example.
Abstract:
The present invention relates to a process for application of chemicals on textile materials for removing surface chemicals and finishes from textile materials which comprises the following steps: reducing the textile materials to an appropriate size; applying a first catalyzed vapor to the textile materials at a predetermined temperature; penetrating the textile materials at a predetermined temperature; applying a second catalyzed vapor to the textile materials; blending the textile materials; applying a third catalyzed vapor to the textile materials in the one or more blending boxes and dwelling the fabric at a predetermined temperature for a predetermined period of time; and applying a blast of cool air to the one or more blending boxes to stop chemical actions in the textile materials and then transporting the textile materials to next station for further deconstruction processing.
Abstract:
A changing device includes a feed component, a winder, a desizing oven, a coating component and a sizing component, and the feed component is provided for supplying a carbon fiber material, and a thermosetting resin oil is covered onto a surface of the carbon fiber material, and a desizing oven is provided for removing the thermosetting resin oil form the surface of the carbon fiber material, and then the coating component coats a surfactant onto the surface of the carbon fiber material, and finally the sizing component is used to coat a thermoplastic resin oil onto a surface of the surfactant to form a carbon fiber product to be wound onto a rewinding part of the winder, so as to produce a carbon fiber product with a thermoplastic resin oil coated onto a surface of the carbon fiber product.
Abstract:
Compositions and textile sizes based on those compositions, which are particular poly(vinyl alcohol) copolymer ionomers, as well as blends of those ionomers with other sizing polymers are described. A process to prepare the ionomers is described. The compositions are poly(vinyl alcohol) copolymers which have carboxylic acid ionomer comonomer units. Sizes based on these ionomers are aqueous solutions of the ionomers or solutions of blends of them with other poly(vinyl alcohol) polymers which are not ionomeric, or solution/suspensions of the ionomers with various starches, or both. Desizing in either water or caustic solutions is generally far superior to comparable polymer blends which contain no poly(vinyl alcohol) copolymer ionomer.
Abstract:
There is provided a process for manufacturing woven or knitted fabrics comprising modifying the woven or knitted fabrics by applying a skeleton triazine cross-linking reaction using a sericin fixing method of raw silk to enhance its shrink and crease resistance and shape stability and thereafter removing the sericin using a special scouring. The process for manufacturing a woven or knitted fabric, comprises the steps of finishing and treating raw silk and/or cellulose fibers by using a silk sericin fixing method; doubling and twisting thus finished/treated raw silk and/or cellulose fibers; weaving or knitting the doubled and twisted yarns; swelling the woven or knitted fabric forming a cloth by dipping it in a bath; and, scouring the woven or knitted fabric swelled in the bath with an enzyme whereby the woven or knitted fabric is provided with shrink and crease resistance and shape stability.
Abstract:
Mixtures of various starch-degrading enzymes (amylases) which comprise at least one high temperature amylase (HTA) and at least one low temperature amylase (LTA) in an activity ratio of HTA to LTA of 10%:90% to 90%:10% develop at least 60% of their maximum activity in the temperature range from 30.degree. to 90.degree. C. Such mixtures can be diluted with water and treated with customary additives. These mixtures are suitable for desizing textiles sized with starch by treatment of the textiles with the mixtures mentioned and subsequent rinsing.
Abstract:
There are disclosed graft polyesters useful as adhesives and coatings and especially useful in processes for sizing spun and continuous filament synthetic organic and inorganic fibrous yarn. One embodiment of the invention is a textile size composition having free carboxyl groups which is prepared in situ on a textile yarn by the application of heat or radiation to a mixture of an unsaturated polyester reactant and a monovinyl monomer reactant comprising an acidic monovinyl monomer having at least one carboxyl group or mixtures thereof with any monovinyl monomer. Desizing can be accomplished by partial neutralization of the size to a pH of at least 6 by reacting the size with a base to render the graft polyester water-dispersible or water-soluble.The graft polyester compositions of the invention are especially useful as size compositions since they can be applied to the yarn from a solventless mixture and require only at least one of the application of heat or irradiation to graft polymerize the size in situ on the yarn. The graft polyester of the invention comprises the reaction product of (1) an unsaturated polyester which is the reaction product of at least one polycarboxylic acid reactant, preferably a dicarboxylic acid reactant and at least one polyhydric alcohol reactant, preferably a diol, wherein a minor effective proportion of at least one of said reactants is .alpha.,.beta.-ethylenically unsaturated with (2) at least one monovinyl monomer reactant comprising at least one acidic monovinyl monomer containing at least one carboxyl group or a mixture of said vinyl monomer with any monovinyl monomer.Alternatively, where water-insolubility is desired in the graft polyester under both acid and basic conditions, a polyunsturated vinyl monomer is utilized having two or more vinyl groups per molecule. The graft polyesters of the invention prepared using monovinyl monomers also can be reacted with cross-linking resins, such as aminoplast resins, to confer water-insolubility under both basic and acid conditions.