Abstract: A radiation-resistant high molecular composition is disclosed, charqacterized in that, to the high molecular polymer, a halogenated acenaphtylene and/or condensates thereof represented by a following general formula [I] ##STR1## (wherein, X indicates a chlorine or bromine atom, a indicates 0 to 2, b indicates 1 to 6 and n indicates an integer not less than 1) and a diphenyl ether derivative represented by a following general formula [II] ##STR2## (wherein, R.sub.1 and R.sub.2 indicate any ones of hydrogen atom, alkyl, alkoxy, phenyl phenoxy, diphenyloxy and terphenyloxy group) and/or basic lead compound are formulated.

Abstract: Process for producing fluorine-containing aliphatic carboxylic acids having the general formula of Y--R.sub.f --Y' as defined herein by reaction of fluorine-containing aliphatic halogen compounds having the general formula of X--R.sub.4 --X' as defined herein with carbon dioxide under the presence of zinc in an organic solvent and hydrolysis of the reaction product, wherein the improvement comprises controlling the concentration of carbon dioxide in the organic solvent at a level of 0.3 to 5 mol/l.

Abstract: A process for producing polyethylenepolyamine from ethylene dichloride and aqueous ammonia which comprises reacting ethylene dichloride with ammonia, and then continuing the reaction in the presence of at least one kind of amine when the overall conversion of ethylene dichloride has become 25 to 85%.

Abstract: A para-substituted halogenobenzene derivative is prepared by halogenating a benzene derivative in the liquid phase in the presence of a molded zeolite catalyst body comprising, based on the weight of the molded zeolite catalyst body, 10 to 95% by weight of an L-type zeolite as the anhydrous state and 5 to 90% by weight of amorphous silica.

Abstract: Ammonia and/or an alkyleneamine is reacted with an alkanolamine by using a miobium-containing substance as a catalyst to obtain an alkyleneamine having an increased number of alkylene units. The niobium-containing substance has a high activity and a high heat resistance, and is not or only slightly soluble in the water-containing reaction liquid.

Abstract: A radiation-resistant high molecular composition is disclosed, characterized in that, to the high molecular polymer, a halogenated acenaphtylene and/or condensates thereof represented by a following general formula [I] ##STR1## (wherein, X indicates a chlorine or bromine atom, a indicates 0 to 2, b indicates 1 to 6 and n indicates an integer not less than 1) and a diphenyl ether derivative represented by a following general formula [II] ##STR2## (wherein, R.sub.1 and R.sub.2 indicate any ones of hydrogen atom, alkyl, alkoxy, phenyl phenoxy, diphenyloxy and terphenyloxy group) and/or basic lead compound are formulated.

Abstract: A process for producing brominated acenaphthylene condensates of the formula: ##STR1## wherein x is 1 or 2, y is an integer from 1 to 6 and n is 1 or more, from elementary units of the following formulas: ##STR2## wherein y is as defined above, comprising, (A) brominating the side chain of the acenaphthene with 0.2 to 2.0 times as many moles of bromine as acenaphthene, said bromination initiated by ultraviolet radiation or by a radical initiator in a halogenated hydrocarbon solvent, (B) adding a Lewis acid catalyst to the reaction solution of step (A) to promote the condensation of the brominated acenaphthene product of step (A), (C) adding to the reaction solution of step (B) an equimolar or more amount of bromine relative to the amount of acenaphthene starting material, to further brominate and condense the brominated acenaphthene and/or brominated acenaphthene condensates; and (D) dehydrobrominating the brominated acenaphthene condensates.

Abstract: A p-substituted halobenzene derivative, which is very valuable in industry, can be obtained by halogenation of benzene and/or a benzene derivative in the liquid phase using, as a catalyst, a faujasite type zeolite in the presence of any one member selected from the group consisting of sulfur-containing compounds, nitrogen-containing organic basic compounds, salts of said nitrogen-containing organic basic compounds, and a mixture of said nitrogen-containing organic basic compounds and salts thereof.

Abstract: p-Substituted halogenated benzene derivatives are prepared at a high selectivity by halogenating benzene and/or benzene derivatives by using as a catalyst a zeolite modified with a metal salt.

Abstract: Process for producing polyamines by a catalytic reduction reaction of a cyanoethylated N-(2-aminoethyl)piperazine and cyanoethylated compounds of polyamines containing 4 or more amino groups in the molecule.

Abstract: In the liquid phase chlorination of benzene derivatives including benzene per se in the presence of a zeolite possessing the main pores having the opening formed of a 12-membered oxygen ring; para-substituted chlorinated benzene derivatives are preferentially obtained by adding a small quantity of a quaternary ammonium salt or salts to the reaction mixture.

Abstract: A process for recovering brominated acenaphthylene and its condensate in the form of powder, comprising dropping a solution of brominated acenaphthylene and its condensate produced from acenaphthene by reactions of bromination, condensation and dehydrobromination into hot water containing a carboxylic acid ester of polyoxyalkylene sorbitan, while the solvent is being distilled off, to recover the brominated acenaphthylene and its condensate in the form of powder dispersed in water.

Abstract: A p-substituted halobenzene derivative, which is very valuable in industry, can be obtained by halogenation of benzene and/or a benzene derivative in a liquid phase at a temperature of 0.degree. to 200.degree. C. at a higher selectivity and yield than in known processes, using, as a catalyst, an L type zeolite alkali-treated with an alkali solution of pH 11 or above at a temperature of 0.degree. to 100.degree. C. for 0.5 to 100 hours.

Abstract: Process for producing condensed bromoacenaphthylene comprising:(A) a step of brominating and condensating acenaphthene with bromine in a halogenated hydrocarbon solvent in the presence of a Lewis acid catalyst;(B) a step of removing the Lewis acid catalyst and then continuing the bromination with bromine with an added radical initiator; and(C) a step of carrying out dehydrobromination reaction.In a modified process, the bromination is effected in a halogenated hydrocarbon solvent at a temperature not lower than 60.degree. C. using bromine at least 3 times as much in moles as acenaphthene in the presence of an iron catalyst.Further, the condensed bromoacenaphthylene is purified by bringing it into contact with an adsorbent in an organic solvent.

Abstract: An improved process for preparing a bis [.beta.-(N,N-dimethylamino)ethyl]ether by reacting a bismethohalide of bis [.beta.-(N,N-dimethylamino)ethyl]ether represented by the following general formula: ##STR1## (wherein X denotes a halogen atom), with an aliphatic amine having a boiling point of not lower than 220.degree. C. at atmospheric pressure and having a primary amino group in the molecule thereof. The process comprises the following two steps (a) and (b): (a) a step of distilling out water at a temperature of not more than 130.degree. C. under reduced pressure from a mixture of said bismethohalide aqueous solution and said aliphatic amine to provide a concentration of said bismethohalide to water of not less than 85% by weight, and (b) a step of reacting said bismethohalide and amine in a solid-liquid phase at a temperature of not lower than 140.degree. C.

Abstract: The disclosed catalyst for polyurethane comprises an organic carboxylic acid salt of a tertiary amine compound and 1-methyl-4-(2-dimethylaminoethyl)piperazine. The tertiary amine compound is selected from the group of triethylenediamine, bis(2-dimethylaminoethyl)ether and N,N,N',N",N"-pentamethyldiethylenetriamine and the organic carboxylic acid is selected from the organic carboxylic acids having 1-20 carbon atoms.

Abstract: Olefins are hydrated to the corresponding alcohols in the presence of at least one crystalline alumino-silicate selected from offretite, ferrierite and erionite. The offretite, ferrierite and erionite are preferably characterized by X-ray diffraction patterns shown in Tables 1 and 7; Tables 2, 8 and 9; and Table 3, respectively. At least a part of the exchangeable cations in the offretite, ferrierite and erionite may be exchanged with at least one cation selected from a hydrogen ion, an alkaline earth metal ion and a rare earth metal ion. Furthermore, at least a part of the exchangeable cations in the erionite may be exchanged with an ammonium ion and/or an alkali metal ion.

Abstract: A method for preparing a bis[.beta.-(N,N-dimethylamino)alkyl]ether by reacting a bismethohalide of bis[.beta.-(N,N-dimethylamino)alkyl]ether represented by the following general formula ##STR1## (wherein R and R' denote alkyl groups having 2-3 carbon atoms, and X denotes halogen atom,) with the aliphatic amine having 40.degree.-170.degree. C. of boiling point at atmospheric pressure and having one or two primary amino group in a molecule thereof at an increased pressure.

Abstract: A method for preparing bis[.beta.-(N,N-dimethylamino)ethyl]ether characterized by performing a one stage reaction at a temperature of below 100.degree. C. wherein vapor of sulfuric anhydride is being introduced into a mixed solution consisting of sodium N,N-dimethylaminoethoxide, N,N-dimethylethanolamine and dioxane.

Abstract: A trans-[hydridocarbonyl tris(triorganic phosphine) rhodium (I)]is produced by reducing a trans-[chlorocarbonyl bis(triorganic phosphine) rhodium (I)]with a tetrahydroborate in the presence of a triorganic phosphine in a solvent by heating, an improvement characterized in that the reduction is carried out in the presence of carbon monoxide or a mixture of more than 50 vol. % of carbon monoxide and an inert gas and the reaction mixture if cooled to O.degree. to 30.degree. C. in an atmosphere of carbon monoxide or a mixture of more than 50 vol. % of carbon monoxide and an inert gas and the crystal is separated. The trans-[hydridocarbonyl tris(triorganic phosphine) rhodium (I)]having high purity is obtained at high yield.