Abstract: To provide electrolytic manganese dioxide excellent in cell performance in high rate discharge and middle rate discharge when used as a cathode material for alkaline manganese dry cells, and a method for its production. Electrolytic manganese dioxide, characterized in that the average size of mesopores is at least 6.5 nm and at most 10 nm, and the alkali potential is at least 290 mV and at most 350 mV; a method for its production and its application.

Abstract: To provide electrolytic manganese dioxide excellent in packing property and high-rate discharge characteristics when used as a cathode material for alkaline dry cells. Electrolytic manganese dioxide in which the half-value width of the (110) plane in XRD measurement using CuK? line as the radiation source is at least 1.8° and less than 2.2°, the peak intensity ratio of X-ray diffraction peaks (110)/(021) is at least 0.70 and at most 1.00, and the JIS-pH (JIS K1467) is at least 1.5 and less than 5.0; a method for producing the electrolytic manganese dioxide; and its application.

Abstract: To provide electrolytic manganese dioxide excellent in packing property and high-rate discharge characteristics when used as a cathode material for alkaline dry cells. Electrolytic manganese dioxide in which the half-value width of the (110) plane in XRD measurement using CuK? line as the radiation source is at least 1.8° and less than 2.2°, the peak intensity ratio of X-ray diffraction peaks (110)/(021) is at least 0.70 and at most 1.00, and the JIS-pH (JIS K1467) is at least 1.5 and less than 5.0; a method for producing the electrolytic manganese dioxide; and its application.

Abstract: A subject for the invention relates to providing a positive active material for lithium ion secondary batteries which attains a high discharge capacity and is excellent in rate characteristics and cycle characteristics. A feature of the invention resides in that a lithium-nickel-manganese composite oxide which has a composition represented by LixNiyMnzO2 wherein x is 1+1/9±(1+1/9)/10, y is 4/9±(4/9)/10, and z is 4/9±(4/9)/10, in particular, represented by the general formula Li[Ni0.5-0.5XMn0.5-0.5XLiX]O2 wherein X satisfies 0.05?X?0.11, and has a crystal structure belonging to the monoclinic system and having a space group of C12/ml (No. 12) is used as a positive-electrode material. The lithium-nickel-manganese composite oxide preferably is one in which in X-ray powder diffractometry using a Cu—K? ray, the peak intensity ratio I(002)/I(13-3) between the (002) plane and the (13-3) plane in terms of Miller indexes hkl on the assumption of belonging to C12/ml (No. 12) of the monoclinic system is 1.35 or higher.

Abstract: A lithium-manganese complex oxide represented by a formula Li[Mn2-X-YLiXMY]O4+&dgr; (wherein M is at least one element selected from the groups IIa, IIIb and VIII of the 3rd and 4th periods, and 0.02≦X≦0.10, 0.05≦Y≦0.30 and −0.2≦&dgr;<0.2), having a spinel crystalline structure of 0.22° or less of half value width of the (400) plane of powder X-ray diffraction by CuK&agr; and an average diameter of crystal grains by SEM observation of 2 &mgr;m or less, and a spinel crystalline structure lithium-manganese complex oxide having a BET specific surface area of 1.0 m2·g−1 or less; production methods thereof; and a lithium secondary battery which uses the lithium-manganese complex oxide as the positive electrode active material are described.

Abstract: A lithium-manganese complex oxide represented by a formula Li[Mn2−X−YLiXMY]O4+&dgr; (wherein M is at least one element selected from the groups IIa, IIIb and VIII of the 3rd and 4th periods, and 0.02≦X≦0.10, 0.05≦Y≦0.30 and −0.2≦&dgr;<0.2), having a spinel crystalline structure of 0.22° or less of half value width of the (400) plane of powder X-ray diffraction by CuK&agr; and an average diameter of crystal grains by SEM observation of 2 &mgr;m or less, and a spinel crystalline structure lithium-manganese complex oxide having a BET specific surface area of 1.0 m2·g−1 or less; production methods thereof; and a lithium secondary battery which uses the lithium-manganese complex oxide as the positive electrode active material are described.

Abstract: There is provided a process for preparing a heteroaromatic aldehyde by catalytic reaction of alkyl-substituted heteroaromatic compound with molecular oxygen in a gaseous phase in the presence of a catalyst, which comprises employing an oxide containing vanadium, phosphorus, aluminium and silicon as a catalyst, and diluting a part or all of the oxide present as a catalyst layer in a reactor with a solid inert to the reaction.

Abstract: A method for producing a heterocyclic nitrile in high yield by a gas-phase catalytic reaction of a heterocyclic carboxylic acid or an ester thereof with ammonia in the presence of a catalyst comprising an oxide of at least one element selected from copper and zinc, and an effective method for producing a heterocyclic aldehyde, using the heterocyclic nitrile thus obtained as a starting material, are provided.

Abstract: A method for producing pyridine bases which gives improved yield and comprises reacting in a gas-phase an aliphatic aldehyde, aliphatic ketone or mixture thereof with ammonia in the presence of a zeolite containing titanium and/or cobalt and silicon as zeolite constituent elements in which the atomic ratio of silicon to titanium and/or cobalt is about 5 to about 1000.

Abstract: A method for producing a heterocyclic nitrile in high yield by a gas-phase catalytic reaction of a heterocyclic carboxylic acid or an ester thereof with ammonia in the presence of a catalyst comprising an oxide of at least one element selected from copper and zinc, and an effective method for producing a heterocyclic aldehyde, using the heterocyclic nitrile thus obtained as a starting material, are provided.

Abstract: A process for producing a pyrazine compound of the general formula (3): ##STR1## wherein R.sup.1, R.sup.2, R.sup.3 and R.sup.4 represent a hydrogen atom or a lower alkyl group, which comprises catalytically reacting in a gaseous phase a diamine compound of the general formula: ##STR2## with a diol compound of the general formula: ##STR3## in the presence of a catalyst containing hydrogen-treated silver or a catalyst containing silver and at least one element selected from the group consisting of alkali metals, alkaline earth metals, zinc and lanthanoid elements.

Abstract: A process for preparing monoallylamine represented by the formula (II):CH.sub.2 .dbd.CHCH.sub.2 NH.sub.2 (II)which comprises: catalytically reacting isopropanolamine represented by the formula (I): ##STR1## in a gaseous phase in the presence of a catalyst having dehydrating property. According to the preparation process of the present invention, monoallylamine can be easily obtained in high selectivity and high yield.

Abstract: A heteroaromatic nitrile is prepared in high conversion and yield by catalytically reacting an alkyl-substituted heteroaromatic compound with molecular oxygen and ammonia in the presence of a catalyst having the following composition:Mo(P).sub.x (A).sub.y (B).sub.z (O).sub.w (I)wherein x, y, z and w represent atomic ratios of phosphorus, an element A defined below, an element B defined below and oxygen to molybdenum, respectively and(i) x and z are both 0 (zero), y is from 0.1 to 5, and A is at least one element selected from the group consisting of cerium and tungsten, or(ii) x is from 0.1 to 7, y is from 0 to 5, z is from 0 to 5, A is at least one element selected from the group consisting of cerium, manganese and tungsten, and B is at least one element selected from the group consisting of thallium, titanium, niobium and aluminum, or(iii) x is from 0.5 to 7, y is from 0 to 5, z is from 0.01 to 2.

Abstract: A heteroaromatic nitrile is prepared in a high selectivity and yield by catalytically reacting an alkyl-substituted heteroaromatic compound with molecular oxygen and ammonia in a molar ratio of oxygen to ammonia of not larger than 1.6:1 in a gaseous phase in the presence of a catalyst comprising a vanadium-phosphorus oxide of the formula:VP.sub.x Sb.sub.y O.sub.z (I)wherein x, y and z represent atomic ratios of phosphorus, antimony and oxygen to vanadium, respectively, and x is from 0.1 to 5, y is 0 to 8 and z is defined from the valencies of other elements.