A method for preparing an anti-bacterial and anti-ultraviolet multifunctional chemical fiber includes: dissolving several soluble metal salts and a polymer complexing dispersant into water to prepare an aqueous solution; adding into a polymer monomer; reacting under microwave or hydrothermal action to obtain a polymer monomer containing multifunctional nano oxides; adding the polymer monomer with other monomer, catalyst, initiator, stabilizer, and the like into a polymerization reactor; and carrying out esterification, polycondensation or copolymerization to obtain a polymer melt, and carrying out spinning or ribbon casting and granule cutting to obtain an anti-bacterial and anti-ultraviolet multifunctional chemical fiber or masterbatch chips. By generating nano metal oxides in the monomer in situ before the polymerization reaction, small particle sizes and dispersibility of the nano metal oxide are ensured; the chemical fiber has efficient, durable antibacterial and anti-ultraviolet functions and is free of metal ion precipitation.

A task is to provide a cloth which is advantageous in that the cloth has extremely excellent flame retardancy, and further has excellent washing shrinkage resistance and excellent hand as well as excellent antistatic properties, preferably in that the whole of the cloth can be uniformly dyed, and a fiber product, and the task is achieved by obtaining a cloth using a spun yarn which comprises a meta-type wholly aromatic polyamide fiber, a modacrylic fiber, and a conductive fiber.

The present invention is generally concerned with the use of additives in the form of nanoclays and/or organoclays as processing and property enhancers in melt-spinning formulations based on particular types of co-polyamides, which are used in the melt-spinning of fibers. The melt-spinning formulations of the present invention may comprise, consist essentially of, or consist of: (i) at least one co-polyamide and (ii) at least one nanoclay and/or organoclay.

The present invention is generally concerned with the use of additives in the form of nanoclays and/or organoclays as processing and property enhancers in melt-spinning formulations based on particular types of co-polyamides, which are used in the melt-spinning of fibers. The melt-spinning formulations of the present invention may comprise, consist essentially of, or consist of: (i) at least one co-polyamide and (ii) at least one nanoclay and/or organoclay.

The present invention concerns yarn comprising polymer, the polymer comprising imidazole groups, the yarn having a sulfur content of 0.01 to 3.0 percent by weight, based on weight of the yarn, the yarn having a tenacity of 30 cN/dtex (33.3 gpd) or higher.

A wholly aromatic polyamide fiber has a reduced total fineness and a reduced single yarn fineness and is also excellent in quality and reinforcing property. The wholly aromatic polyamide fiber is characterized in that it has a single yarn fineness of 0. 4 dtex to 3. 5 dtex, a total fineness of 5 dtex to 30 dtex, a breaking strength of 15 cN/dtex or more, an initial tensile modulus of 500 cN/dtex to 750 cN/dtex, and the number of fibrils of less than 100/m.

A resin powder for solid freeform fabrication includes a particle having a pillar-like form, wherein the ratio of the height of the particle to the diameter or the long side of the bottom of the particle is 0.5 to 2.0, the particle has a 50 percent cumulative volume particle diameter of from 5 to 200 μm, and the ratio (Mv/Mn) of the volume average particle diameter (Mv) to the number average particle diameter (Mn) of the particle is 2.00 or less.

A resin powder for solid freeform fabrication includes a particle having a pillar-like form, wherein the ratio of the height of the particle to the diameter or the long side of the bottom of the particle is 0.5 to 2.0, the particle has a 50 percent cumulative volume particle diameter of from 5 to 200 μm, and the ratio (Mv/Mn) of the volume average particle diameter (Mv) to the number average particle diameter (Mn) of the particle is 2.00 or less.

The invention relates to a method for the preparation of a polyamide 6 copolymer, characterised in that a copolymerization reaction is carried out between: o at least one caprolactam of formula (I): o at least one caprolactam, named substituted caprolactam, in which at least one of the carbon atoms is covalently linked to at least one A moiety, said A moiety being selected from the group formed of: # moieties comprising at least one group of formula: (A) # moieties comprising at least one group of formula: (B) # moieties comprising at least one group of formula: (C) The invention also relates to a polyamide 6, to polyamide 6 filaments and filaments yarns.

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The invention relates to a method for the preparation of a polyamide 6 copolymer, characterised in that a copolymerization reaction is carried out between: o at least one caprolactam of formula (I): o at least one caprolactam, named substituted caprolactam, in which at least one of the carbon atoms is covalently linked to at least one A moiety, said A moiety being selected from the group formed of: # moieties comprising at least one group of formula: (A) # moieties comprising at least one group of formula: (B) # moieties comprising at least one group of formula: (C) The invention also relates to a polyamide 6, to polyamide 6 filaments and filaments yarns.

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