Abstract:
Halogen containing synthetic resin compositions, particularly polyvinyl halide compositions, are stabilized against deterioration by light and heat by the addition of a condensation product of an organotin oxide, hydroxide, halide or a hydrocarbon-substituted stannoic acid with a dimercaptoacid ester of an organic diol of formula:-Rx Sn(S-A-OOC-B-COO-A-SH)4-x wherein x is 1, 2 or 3, R is a univalent hydrocarbon radical (especially alkyl, aryl, alkaryl or aralkyl), A and B are each divalent hydrocarbon radicals respectively containing up to 20 carbon atoms, the sum of the carbon atoms in A-B being not more than 25. Plasticizers may also be present in the compositions. Typical stabilizers specified include dibutyltin- -bis-S, S1-(1, 4-butyleneglycol dimercaptoacetate), -bis-S, S1-(1, 5-pentanediol dimercaptoacetate), -bis-S, S1-(1, 8-octanediol dimercaptoacetate), and -bis-S, S1-(1-ethyl-1, 3-hexane diol dimercaptoacetate : trioctyltin-diethylene glycol di-5-mercaptovalerate: triphenyltin and tri-benzyltin-S-ethylene glycol dimercapto acetate and butyltin tris-S, S1, S11 (propylene glycol di-b -mercapto butyrate).ALSO:The invention comprises organotin compounds of formula: RxSn(S-A-OOC-B-COO-A-SH)4-x wherein x is 1, 2 or 3, R is a univalent hydrocarbon radical (e.g. alkyl, aryl, alkaryl, aralkyl) containing up to 10 carbon atoms, A and B are each divalent hydrocarbon radicals respectively containing up to 20 carbon atoms, the sum of the carbon atoms in A and B not exceeding 25. They may be prepared by condensing an organotin oxide, hydroxide, halide or hydrocarbon substituted stannoic acid with the dimercaptoacid ester, in the presence if necessary of a halogen acceptor such as an alkaline hydroxide, alkali metal carbonate, ammonia or an amine. R in the formula above may be butyl, octyl or phenyl. Preferred diols include ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, 2-ethyl-2-butyl-1,3-propanediol, 2,2-diethyl-1,3-propanediol, 2-ethyl-1,3-hexanediol, hexylene glycol, 1,5-pentanediol, 12-hydroxystearyl alcohol, 1,10 dodecanediol. Specified mercapto acid which may be esterified include mercapto acetic acid, b -mercaptopropionic acid, thiosalicylic acid, a -mercaptopropionic acid, mercaptobutyric acid, mercaptovaleric acid, a -mercaptostearic acid, a -mercaptocaprylic, a -mercaptopelargonic acid, a -mercaptolauric acid, a -mercaptopalmitic acid, a -mercaptophenylacetic acid, a -mercaptodiphenylacetic acid, a -mercaptodiethylacetic acid, 5-mercaptovaleric acid, 6-mercaptocaproic acid, 8-mercaptocaprylic acid and 12-mercaptolouric acid. The reaction may take place at temperatures between room temperature and 50 DEG C. (the water produced being removed by additional heating) under an inert atmosphere and in the presence of an inert solvent such as benzene, toluene or methyl alcohol. The preparation of the following compounds is described: dibutyl tin bis-S,S1-(ethylene glycol dimercapto acetate), tributyl tin S-diethylene glycol di-5-mercaptovalerate, trioctyl tin-S-diethylene glycol di-5-mercaptovalerate, triphenyl tin and tribenzyl tin-S-ethylene glycol-dimercaptoacetate, dibutyltin and dioctyl tin bis(1,4-butylone glycol dimercaptoacetate), dibutyl tin-bis-1,5 pentanediol dimercaptoaceaate)-bis(1,8-octanediol dimercaptoacetate), and -bis-(1-ethyl-1,3-hexanediol dimercaptoacetate, di-ethylhexyltin bis-(ethylone glycoldimercaptoacetate) and butyl tin-bisS,S1,S11(propylene glycol di-b -mercaptobutyrate). The compounds of the invention may be used in halogen-containing synthetic resin compositions as stabilisers against deterioration by light and heat. Dimercapto acid esters of organic diols. Mercaptoacetic acid is reacted with ethylene glycol in toluene solution using p-toluene sulphonic acid as esterification catalyst. Reference is also made to the preparation of ethylene glycol-di-12-mercapto stearate and -di-5-mercapto valerate from ethylene glycol and 12 mercaptostearic acid and 5-mercaptovaleric acid respectively: propylene glycol dib -mercaptobutyrate from propylene glycol and b -mercaptobutyric acid: 2-ethyl-2-butyl-1,3-propanediol di-thiosalicylate from 2-ethyl-2-butyl-1,3-propanediol and thiosalicylic acid: and 12-hydroxystearyl alcohol dimercaptoacetate from 12-hydroxystearyl alcohol and mercaptoacetic acid.
Abstract:
The resistance to both flaming and glowing combustion exhibited by polymer compositions wherein the flame retarding agent is comprised at least in part of a halogen-containing organic compound in combination with an antimony oxide is significantly increased by including specified halogenated phosphates, thiophosphates or thiophosphoryl chlorides as part of the flame retarding agent. The presence of sulfur in the composition reduces the total amount of flame retarding agent required to achieve an SE-O rating in the UL 94 vertical position burning test.
Abstract:
Structural discontinuities, commonly referred to as splits and voids, which are prevalent in flexible and semiflexible polyurethane foams that have been rendered flame resistant using halogen-containing polymers in combination with antimony oxide are eliminated by the use of barium carbonate.
Abstract:
Triorganotin compounds of the general formulae
ARE NOVEL AND EFFECTIVELY COMBAT A VARIETY OF UNDESIRABLE ORGANISMS, INCLUDING FUNGI AND MITES WHEN APPLIED TO OBJECTS, PARTICULARLY PLANTS, THAT ARE SUSCEPTIBLE TO ATTACK BY THESE ORGANISMS. In the foregoing formulae each R is individually selected from hydrogen and lower alkyl radicals, X is a chlorine, bromine, fluorine, hydroxyl, carboxylate, phenoxy, alkoxy (-OR'') or mercaptide (-SR'') radical wherein R'' represents an alkyl or aryl radical containing between 1 and 12 carbon atoms, inclusive; Y is an oxygen, sulfur, or a sulfate radical and n represents an integer between 1 and 5, inclusive.
Abstract:
Strong durable bonds are formed between metals and vinyl chloride-containing polymers by maintaining at a surface of the metal a layer of polymer that contains pendant carboxylic acid
GROUPS. One surface of the polymer layer has been modified by oxidation or chemical etching agents. Between the modified surface of the polymer layer and the vinyl chloride-containing polymer is an adhesive comprising a mixture of a natural or synthetic rubber and a phenolaldehyde resin. Heating the composite above 120*C. for a short period of time yields a unitary bonded structure.
Abstract:
In accordance with certain of its aspects, this invention relates to novel compositions and to a process for preparing an article having a textured coating which comprises bonding to a substrate a self-adhering coating composition containing: (A) 16.0 - 34.2 PARTS BY WEIGHT OF A FIRST VINYL RESIN HAVING A RELATIVE VISCOSTY OF 1.98 - 2.35; A MOLECULAR WEIGHT OF ABOUT 75,000 - 101,000, AND AN AVERAGE PARTICLE SIZE OF ABOUT 0.5 - 7.0 MICRONS; (B) 3.8 - 24.0 PARTS BY WEIGHT OF A SECOND HALOGEN-CONTAINING RESIN HAVING A SPECIFIC VISCOSITY OF ABOUT 0.50, AN INHERENT VISCOSITY OF ABOUT 1.20, A MOLECULAR WEIGHT AVERAGE OF ABOUT 127,000, AND A PARTICLE SIZE RANGE OF AT LEAST 7.0 MICRONS TO 177 MICRONS; (C) 1.0 - 7.6 PARTS BY WEIGHT OF A THIRD VINYL SOLUTION RESIN WITH REACTIVE SITES HAVING A VINYL CHLORIDE CONTENT OF 75.0 TO 91.5 PERCENT COPOLYMERIZED WITH AT LEAST ONE MEMBER SELECTED FROM THE GROUP CONSISTING OF VINYL ACETATE, VINYLIDENE CHLORIDE, OR AN ESTER OF MALEIC ACID, AND HAVING AN INHERENT VISCOSITY OF ABOUT 0.34 - 0.46; (D) 0.2 - 3.8 PARTS BY WEIGHT OF A LIQUID EPOXY RESIN HAVING A VISCOSITY OF ABOUT 10,000 - 20,000 CENTIPOISES AND AN EPOXY EQUIVALENT WEIGHT OF ABOUT 180 - 220; (E) 1.2 - 14.7 PARTS BY WEIGHT OF AN AMINOPLAST RESIN; (F) 17 30.4 PARTS BY WEIGHT OF A PLASTICIZER; (G) ABOUT 0.0 - 15.3 PARTS BY WEIGHT OF A SOLVENTDILUENT WHICH WHEN PRESENT COOPERATES WITH PLASTICIZERS TO DISSOLVE THE THIRD VINYL RESINS (C), THE LIQUID EPOXY RESIN (D), AND THE AMINOPLAST RESIN (E) BUT DOES NOT GEL OR DISSOLVE EITHER THE FIRST VINYL RESIN (A), OR THE SECOND HALOGEN-CONTAINING RESIN (B) AT TEMPERATURES OF ABOUT 20-35*C.; and wherein the first vinyl resin (a) and the second resin (b) are incompletely soluble in plasticizer (f) at temperatures of 20-35*C. and wherein plasticizer (f) is capable of completely solubilizing the third vinyl resin solution (c); (H) 3.0 - 23.7 PARTS BY WEIGHT OF PIGMENTS AND/OR FILLERS; AND, OPTIONALLY (I) 1.6 - 2.5 PARTS BY WEIGHT OF AT LEAST ONE POLYVINYL CHLORIDE STABILIZER, WHEREIN THE TOTAL PARTS BY WEIGHT OF INGREDIENTS (A) - (I) AMOUNTS TO 100 PARTS.
Abstract:
A FLAME RETARDANT SYSTEM IS PROVIDED FOR POLYURETHANE FOAMS COMPRISING AN INERT FILLER, A HALOGEN SOURCE AND A PHOSPHORUS CONTAINING COMPOUND, AND, ALSO, URETHANE FOAM COMPOSITIONS CONTAINING THE FLAME RETARDANT SYSTEMS. IN ADDITION, METHODS ARE PROVIDED FOR MAKING THE SYSTEMS INCLUDING COATING THE INDIVIDUAL PARTICLES OF THE FILLER WITH A COMPOSITION CONTAINING THE HALOGEN SOURCE, AND THEREAFTER ADHERING THE PHOSPHORUS CONTAINING COMPOUND TO THE COATED PARTICLES, AND ALSO, METHODS FOR MAKING THE FLAME RETARDANT URETHANE FOAM COMPOSITIONS.
WHEREIN X IS A HALOGEN;N IS A POSITIVE NUMBER AND PREFERABLY 1-20; M IS A METAL ION HAVING A VALENCE V; AND V IS AN INTEGER 1-7 ARE PREPARED BY REACTING A PHOSPHORUS HALIDE, AN AMMONIUM HALIDE, A HALOGEN AND METAL HALIDE. THE COMPOSITIONS ARE USEFUL AS DAMPING FLUIDS AND AS POLYMERIZATION CATALYSTS.
Abstract:
This invention relates to nickel and stannous salts of cyaniminodithio-carbonic acid of the formula
WHEREIN X is selected from the group consisting of Ni and Sn ; to a method of making said salts, to biological compositions containing said salts as the active agent, and to the use of said salts as biological toxicants.
Abstract translation:本发明涉及式为WHEREIN X ++的氰基亚氨基二硫代碳酸的镍和亚锡盐,其选自Ni ++和Sn ++, 涉及制备所述盐的方法,含有所述盐作为活性剂的生物组合物以及所述盐作为生物毒性物质的用途。