A reactive antibacterial compound and a preparation method thereof are provided herein. The reactive antibacterial compound is represented by the general formula (I) or (II): ##STR00001##
wherein R.sub.1 represents OCN-L-NHCOOR′, OCN-L-NHCONHR′, OCN-L-NHCOSR′, OCN-L-COOR′, or OCN-L-COONHR′. G1 represents OCN-M-NHCOOG′, OCN-M-NHCONHG′, OCN-M-NHCOSG′, OCN-M-COOG′, or OCN-M-COONHG′. L, M, R′ and G′ independently for each occurrence represent divalent alkyl and cycloalkyl having from 1 to 18 carbon atoms, optionally substituted by up to 18 heteroatoms. R.sub.4 and G.sub.4 independently for each occurrence represent a divalent alkyl and cycloalkyl having from 1 to 18 carbon atoms, optionally substituted by at most 18 heteroatoms. G.sub.2 and G.sub.3 independently for each occurrence represent —H, —F, —Cl, —Br, —I, —OCH3, —OCH2CH3, —OPr, —CN, —SCN, —NO, —NO2, a monovalent unsubstituted or substituted alkyl, cycloalkyl, or aryl having from 1 to 7 carbon atoms. Z and X independently for each occurrence represent —COO, —SO3, or —OPO2OR.sub.5. R.sub.5 represents a monovalent unsubstituted or substituted alkyl, cycloalkyl, or aryl having from 1 to 6 carbon atoms.

A reactive antibacterial compound and a preparation method thereof are provided herein. The reactive antibacterial compound is represented by the general formula (I) or (II): ##STR00001##
wherein R.sub.1 represents OCN-L-NHCOOR′, OCN-L-NHCONHR′, OCN-L-NHCOSR′, OCN-L-COOR′, or OCN-L-COONHR′. G1 represents OCN-M-NHCOOG′, OCN-M-NHCONHG′, OCN-M-NHCOSG′, OCN-M-COOG′, or OCN-M-COONHG′. L, M, R′ and G′ independently for each occurrence represent divalent alkyl and cycloalkyl having from 1 to 18 carbon atoms, optionally substituted by up to 18 heteroatoms. R.sub.4 and G.sub.4 independently for each occurrence represent a divalent alkyl and cycloalkyl having from 1 to 18 carbon atoms, optionally substituted by at most 18 heteroatoms. G.sub.2 and G.sub.3 independently for each occurrence represent —H, —F, —Cl, —Br, —I, —OCH3, —OCH2CH3, —OPr, —CN, —SCN, —NO, —NO2, a monovalent unsubstituted or substituted alkyl, cycloalkyl, or aryl having from 1 to 7 carbon atoms. Z and X independently for each occurrence represent —COO, —SO3, or —OPO2OR.sub.5. R.sub.5 represents a monovalent unsubstituted or substituted alkyl, cycloalkyl, or aryl having from 1 to 6 carbon atoms.

The invention is drawn to a method of making a fire-resistant mine-grid comprising the following steps: providing a poly(vinyl chloride) (PVC) plastisol, providing a polyester yarn mesh fabric, coating the polyester yarn mesh fabric with the PVC plastisol, heating the coated fabric for about 5 to 20 minutes, more preferably for about 5 to 15 minutes, to a temperature comprised between 110° C. and 150° C., so as to effect gelatinization of the PVC plastisol and form a plasticized PVC coating enveloping the polyester yarns of the mesh fabric,
wherein the PVC plastisol, comprises (a) a poly(vinyl chloride) base resin, (b) from 60 to 140 phr of a primary plasticizer which is tris-(2-chloro-isopropyl)phosphate (TCPP), (c) from 40 to 140 phr of a secondary plasticizer, (d) from 145 to 230 phr of an inorganic filler.

A bi-profiled fiber and preparing method thereof are provided. The bi-profiled fiber is manufactured through the steps of spinning melt metering, extruding via the composite spinneret, cooling, oiling, drawing, heat setting and winding, finally containing both double-cross monofilaments and circular monofilaments simultaneously. The bi-profiled fiber is made of the modified polyester, and the modified polyester is dispersed by matte agent and is composed of terephthalic acid segments, ethylene glycol segments and branched diol segments, and the branched diol segment has a structural formula of ##STR00001## where R.sub.1 and R.sub.2 are separately selected from the linear alkylene with 1-3 carbon atoms, R.sub.3 from the alkyl with 1-5 carbon atoms, and R.sub.4 from the alkyl with 2-5 carbon atoms. The matte agents is a mixture of amorphous titanium dioxide and amorphous silicon dioxide, or a mixture of calcium carbonate and amorphous silicon dioxide.

A bi-profiled fiber and preparing method thereof are provided. The bi-profiled fiber is manufactured through the steps of spinning melt metering, extruding via the composite spinneret, cooling, oiling, drawing, heat setting and winding, finally containing both double-cross monofilaments and circular monofilaments simultaneously. The bi-profiled fiber is made of the modified polyester, and the modified polyester is dispersed by matte agent and is composed of terephthalic acid segments, ethylene glycol segments and branched diol segments, and the branched diol segment has a structural formula of ##STR00001## where R.sub.1 and R.sub.2 are separately selected from the linear alkylene with 1-3 carbon atoms, R.sub.3 from the alkyl with 1-5 carbon atoms, and R.sub.4 from the alkyl with 2-5 carbon atoms. The matte agents is a mixture of amorphous titanium dioxide and amorphous silicon dioxide, or a mixture of calcium carbonate and amorphous silicon dioxide.

A flame retardant aid includes an amphoteric polymer compound having at least one of a specific cationic unit such as allylamine, and an anionic unit such as maleic acid, and a flame retarding agent composition including the flame retardant aid. A method of producing a flame-retardant fiber fabric includes treating a polyester fiber fabric using a flame retardant aid including a flame retardant component and the above amphoteric polymer compound, and drying the polyester fiber fabric.

It is intended to provide a novel artificial sueded leather having flame retardance, which is excellent inflame retardance, light resistance and abrasion resistance, suffers from no water spot and is free from any halogenated chemical (i.e., one having been treated with a so-called non-halogenated flame retardant), and a method of producing the same. The above artificial sueded leather comprises a thermoplastic synthetic fiber cloth made of a woven fabric, a knitted web or a nonwoven fabric, which has a raised-fiber or napped-fiber surface and has been impregnated with a polyurethane resin, and a flame retardant which contains at least a phosphate compound A having a solubility in water of 1% or less, a vinyl group-containing resin C capable of forming a carbonization skeleton in burning and a water-insoluble thickener D and is imparted to one face of the thermoplastic synthetic fiber cloth. A method of producing the artificial sueded leather as described above comprises imparting an flame retardant, which contains at least a phosphate compound A having a solubility in water of 1% or less, a vinyl group-containing resin C capable of forming a carbonization skeleton in burning and a water-insoluble thickener D, to one face of a thermoplastic synthetic fiber cloth made of a woven fabric, a knitted web or a nonwoven fabric which has a raised-fiber or napped-fiber surface and has been impregnated with a polyurethane resin.

It is intended to provide a novel artificial sueded leather having flame retardance, which is excellent inflame retardance, light resistance and abrasion resistance, suffers from no water spot and is free from any halogenated chemical (i.e., one having been treated with a so-called non-halogenated flame retardant), and a method of producing the same. The above artificial sueded leather comprises a thermoplastic synthetic fiber cloth made of a woven fabric, a knitted web or a nonwoven fabric, which has a raised-fiber or napped-fiber surface and has been impregnated with a polyurethane resin, and a flame retardant which contains at least a phosphate compound A having a solubility in water of 1% or less, a vinyl group-containing resin C capable of forming a carbonization skeleton in burning and a water-insoluble thickener D and is imparted to one face of the thermoplastic synthetic fiber cloth. A method of producing the artificial sueded leather as described above comprises imparting an flame retardant, which contains at least a phosphate compound A having a solubility in water of 1% or less, a vinyl group-containing resin C capable of forming a carbonization skeleton in burning and a water-insoluble thickener D, to one face of a thermoplastic synthetic fiber cloth made of a woven fabric, a knitted web or a nonwoven fabric which has a raised-fiber or napped-fiber surface and has been impregnated with a polyurethane resin.

A polyurethane based filament winding resin reaction mixture, a resin bath and a filament winding apparatus are set forth. The reaction mixture comprises an isocyanate component including one or more isocyanates and an isocyanate-reactive component including from 5 wt % to 95 wt % of one of more polyols having a number acerage molecular weight from 50 g/mol to 8,000 g/mol, from 2 wt % to 30 wt % of one or more propane based triols, and from 1 wt % to 15 wt % of one or more trimester-phosphates, based on the total weight of the isocyanate-reactive component. A ratio of a total weight of the one or more propane based triols to a total weight of the one or more trimester-phosphates is between 1.1 and 5.0.

A method for fusing aramid fibers, wherein a) at least one area of an aramid fiber is treated with an ionic liquid so that the aramid is partially dissolved, b) the aramid fiber is contacted via the dissolved area with another aramid fiber area with pressure being applied to the contact area, and subsequently c) the partially dissolved area of the aramid is re-coagulated.