Abstract: Disclosed is a member of nylon 12 having a relative viscosity of from 1.9 to 3.5 when measured in 98% sulfuric acid at a concentration of 10 g/dm3 and at 25° C. and a melt flow rate of 0.1 g/10 min. or more when measured at 235° C.

Abstract: Disclosed is a member of nylon 12 having a relative viscosity of from 1.9 to 3.5 when measured in 98% sulfuric acid at a concentration of 10 g/dm3 and at 25° C. and a melt flow rate of 0.1 g/10 min. or more when measured at 235° C. under a load of 2,160 g, wherein said relative viscosity and said melt flow rate have a relationship of the following formula (I): 2.87×103 exp (−3.48 &eegr;r)≦MFR≦3.25×104 exp (−3.48 &eegr;r)  (I) wherein &eegr;r is relative viscosity and MFR is melt flow rate. The nylon 12 has excellent extrusion moldability and creep characteristics, fatigue characteristics and the like mechanical properties and is suited for tubular molds. A nylon 12 composition comprising the nylon 12 having the above-described specific relationship between &eegr;r and MFR and a plasticizer is also disclosed.

Abstract: A novel heat-resistant low-silica zeolite, an industrial production process, and uses of the low-silica zeolite are provided. The heat-resistant low-silica zeolite contains Si and Al in a molar ratio of SiO.sub.2 /Al.sub.2 O.sub.3 ranging from 1.9 to 2.1, and has sodium and/or potassium as metal cation, wherein the low-silica zeolite contains low-silica faujasite type zeolite at a content of not lower than 88%, and has a thermal decomposition temperature ranging from 870.degree. C. to 900.degree. C. in the air. The process for producing the heat-resistant low-silica zeolite comprises mixing a solution containing an aluminate with another solution containing a silicate, allowing the resulting mixture to gel, and aging the resulting gel, at the temperature of from 0.degree. C. to 60.degree. C., to prepare a slurry having a viscosity ranging from 10 to 10000 cp and containing amorphous aluminosilicate having a specific surface area of not less than 10 m.sup.2 /g with an SiO.sub.2 /Al.sub.2 O.sub.

Abstract: This invention relates to a housing unit in which a certain unit is provided in a packaging case. The object of the invention is to reduce the number of parts and fabrication steps to lower production cost and to cushioned impact applied to the unit. A disc unit provided in the packaging case is urged by restoring forces of a first, a second and a third pressing portion, which are formed integrally with the packaging case. Also, the disc unit is held down to be secured by a stopper portion which secure disc units of different height.

Abstract: A crystalline zeolite X adsorbent comprising a crystalline zeolite X having an SiO.sub.2 /A.sub.2 O.sub.3 molar ratio of not larger than 3.0, where lithium cations associated with an AlO.sub.2 tetrahedron unit are 80 to less than 88 mol % of the total cations and the content of alkaline earth metal cations is from 0.5 to less than 4.6 mo % is produced by ion-exchanging with lithium cations at least 90 mol % of the cations associated with an Al.sub.2 O.sub.3 tetrahedron unit of a crystalline zeolite X having an SiO.sub.2 /Al.sub.2 O.sub.3 molar ratio of not larger than 3.0, ion-exchanging the crystalline zeolite X again with an aqueous solution of mixed salts of an alkali metal salt and an alkaline earth metal salt to decrease the lithium cations associated with the AlO.sub.2 tetrahedron unit to 80 to less than 88 mol %, followed by washing and drying, and activating the crystalline zeolite X.

Abstract: An ITO sintered body according to the present invention has a density thereof of between 90 and 100% and a sintering particle size of between 1 and 20 .mu.m. A proportion of (In.sub.0.6 Sn.sub.0.4).sub.2 O.sub.3 in the ITO sintered body is 10% or below. Such an ITO sintered body is manufactured by mixing an indium oxide powder, whose BET surface area is between 15 and 30 m.sup.2 /g, a BET size/a crystallite size is 2 or below, and an average primary particle size is between 0.03 and 0.1 .mu.m, with tin oxide whose BET surface area is 3 m.sup.2 /g or below, and then by sintering the mixture.

Abstract: An electroconductive zinc oxide sintered body composed of sintered particles fusion-bonded in the grain boundaries thereof; which has a sintered density of from 5 to 5.5 g/cm.sup.3 ; and which does not substantially contain closed cells isolated from the outside in the interior of the sintered body. The electroconductive zinc oxide sintered body is prepared by sintering a mixture of an oxide of an element having a positive valency of at least 3 and zinc oxide in the presence of water at a temperature of at least 1,300.degree. C. The electroconductive zinc oxide sintered body is used as a sputtering target for the preparation of a low resistance, transparent electroconductive film.

Abstract: An indium oxide powder or indium oxide/tin oxide powder having an average primary particle diameter of 1 to 0.01 .mu.m, a BET surface area of 15 to 50 m.sup.2 /g, and a specific surface area of 2 to 5 m.sup.2 /g as determined from the particle diameter distribution. The mixed powder is prepared by coprecipitating an indium- and tin-containing salt from a solution containing indium and tin, calcining the salt, and pulverizing the calcined product using a specific vibrating pulverizer. A sintered body, prepared by sintering the indium oxide/tin oxide powder, has a density of at least 5.3 g/cm.sup.3, a specific resistance of 2.times.10.sup.-3 to 2.times.10.sup.-4 .OMEGA.-cm, and an average grain diameter of 5 to 15 .mu.m.

Abstract: Undesirable deposition of polyoxymethylene onto the inner wall of a polymerization vessel and onto a stirrer, which deposition is observed in the slurry polymerization of formaldehyde carried out in an inert organic liquid medium in the presence of a polymerization catalyst, can be minimized by carrying out the slurry polymerization in the presence of at least one polyvalent metal salt selected from polyvalent metal salts of alkylsalicylic acids and polyvalent metal salts of dialkyl esters of sulfosuccinic acid. Optionally, a polyethylene glycol monoether may be used in addition to the polyvalent metal salt.