Abstract: A treatment method for reducing carbon dioxide emission of combustion exhaust gas includes: a caustic soda synthesis step; a treatment step of reducing carbon dioxide emission of combustion exhaust gas; and a recycling step. In the caustic soda synthesis step, a natural sodium carbonate aqueous solution (Na2CO3) prepared by dissolving natural sodium carbonate ore powder composed of Na2CO3 and NaHCO3 in a caustic soda aqueous solution is used to generate a caustic soda aqueous solution and calcium carbonate precipitate by a causticization reaction with slaked lime, and solid-liquid separation is performed to obtain a synthetic caustic soda aqueous solution. In the treatment step, the synthetic caustic soda aqueous solution and purified combustion exhaust gas are brought into gas-liquid countercurrent contact so that carbon dioxide in the exhaust gas is absorbed by the synthetic caustic soda aqueous solution and immobilized as sodium carbonate.

Abstract: A treatment method for reducing carbon dioxide emission of combustion exhaust gas includes: a caustic soda synthesis step; a treatment step of reducing carbon dioxide emission of combustion exhaust gas; and a recycling step. In the caustic soda synthesis step, a natural sodium carbonate aqueous solution (Na2CO3) prepared by dissolving natural sodium carbonate ore powder composed of Na2CO3 and NaHCO3 in a caustic soda aqueous solution is used to generate a caustic soda aqueous solution and calcium carbonate precipitate by a causticization reaction with slaked lime, and solid-liquid separation is performed to obtain a synthetic caustic soda aqueous solution. In the treatment step, the synthetic caustic soda aqueous solution and purified combustion exhaust gas are brought into gas-liquid countercurrent contact so that carbon dioxide in the exhaust gas is absorbed by the synthetic caustic soda aqueous solution and immobilized as sodium carbonate.

Abstract: There are provided a pharmaceutical raw material capable of exhibiting a uniform functionality and producing magnetic particle-containing drugs for diagnosis and medical treatments with a high reproducibility. The pharmaceutical raw material comprises a monodisperse colloid sterile aqueous solution of magnetic iron oxide fine particles having an average particle diameter of 5 to 30 nm, a saturation magnetization of 50 to 90 Am2/kg and a coercive force of 0.1 to 1.6 kA/m. The pharmaceutical raw material can be produced by forming magnetic iron oxide fine particles in the form of a colloid aqueous solution, purifying the resultant colloid aqueous solution of superparamagnetic iron oxide particles by water-washing and removing water-soluble salts by-produced upon the reaction from the reaction solution by an ordinary method, and replacing a dispersing medium of the purified colloid aqueous solution with ultrapure water.

Abstract: Disclosed is a gas generant composition for a gas actuator used for activating a safety device, which contains (A) a nitrogen-containing organic compound, (B) a metal nitrate and/or a perchlorate, (C) a water-soluble polymer binder, and (D) a magnetic material. When compared with the conventional gas generant compositions, this gas generant composition is excellent in combustibility under low pressure conditions and reduced in CO gas generation during combustion. In this gas generant composition, (D) the magnetic material is preferably composed of a magnetic iron oxide.

Abstract: There are provided a pharmaceutical raw material capable of exhibiting a uniform functionality and producing magnetic particle-containing drugs for diagnosis and medical treatments with a high reproducibility. The pharmaceutical raw material comprises a monodisperse colloid sterile aqueous solution of magnetic iron oxide fine particles having an average particle diameter of 5 to 30 nm, a saturation magnetization of 50 to 90 Am2/kg and a coercive force of 0.1 to 1.6 kA/m. The pharmaceutical raw material can be produced by forming magnetic iron oxide fine particles in the form of a colloid aqueous solution, purifying the resultant colloid aqueous solution of superparamagnetic iron oxide particles by water-washing and removing water-soluble salts by-produced upon the reaction from the reaction solution by an ordinary method, and replacing a dispersing medium of the purified colloid aqueous solution with ultrapure water.

Abstract: The magneto rheological fluid of the present invention comprises magnetic particles, a dispersing medium and polyethyleneoxide as a viscosity modifier, the polyethyleneoxide being contained in an amount of 0.5 to 5% by weight based on the weight of the magnetic particles. The magneto rheological fluid of the present invention can exhibit an excellent dispersion stability, and, more specifically, can exhibit an excellent dispersion stability and can be prevented from suffering from sedimentation of magnetic particles contained therein.

Abstract: The disclosure describes plastic formed products comprising:one selected from the group consisting of a thermoplastic resin and a thermosetting resin; and0.1 to 10 wt % of at least one selected from the group consisting of ferric oxide hydroxide particles, hematite particles, magnetite particles and maghemite particles;wherein (1) the average major axial diameter or the plate diameter of said ferric oxide hydroxide particles is 0.02 or 2.0 .mu.m and the average aspect ratio or the plate ratio thereof is 2 to 20, (2) the average particle size of said hematite particles, magnetite particles and maghemite particles is 0.01 to 1.0, the BET specific surface area thereof is 1 to 120 m.sup.2 /g and the water content on the surfaces thereof is not less than 0.02 wt %/m.sup.2 /g.

Abstract: A heat-resistant inorganic pigment of the present invention comprises a composite metal oxide containing Ti and two divalent metals selected from the group consisting of Mg, Fe, Ni and Co, the content of said two divalent metals in said composite metal oxide being 0.95 to 1.05, in an atomic ratio, based on Ti, and the composition ratio of said two divalent metals being 95/5 to 5/95 in an atomic ratio. The pigment of the present invention is useful as a pigment for a heat-resistant coating material and is a novel heat-resistant inorganic pigment which does not pollute the environment.

Abstract: The disclosure describes plastic formed products comprising:one selected from the group consisting of a thermoplastic resin and a thermosetting resin; and0.1 to 10 wt % of at least one selected from the group consisting of ferric oxide hydroxide particles, hematite particles, magnetite particles and maghemite particles;wherein (1) the average major axial diameter or the plate diameter of said ferric oxide hydroxide particles is 0.02 or 2.0 .mu.m and the average aspect ratio or the plate ratio thereof is 2 to 20, (2) the average particle size of said hematite particles, magnetite particles and maghemite particles is 0.01 to 1.0, the BET specific surface area thereof is 1 to 120 m.sup.2 /g and the water content on the surfaces thereof is not less than 0.02 wt %/m.sup.2 /g.

Abstract: Disclosed herein are magnetic composite iron oxide particles comprising spinel-type Fe.sub.3 O.sub.4 particles as core particles and spinel-type CoFe.sub.2 O.sub.4 outerlayer of the composite iron oxide particles, a process for producing the same, and a magnetic recording medium comprising a substrate and a magnetic recording layer containing the said magnetic iron oxide particles.

Abstract: Disclosed herein is superparamagnetic fine particles of iron oxide having an unsaturated fatty acid adsorbed on the surface of superparamagnetic fine particles and having a magnetization of not less than 50 emu/g, the rate of change of the magnetization of not more than 10%, and an Fe.sup.2+ content (calculated as Fe.sup.2+ /Fe.sup.3+ molar ratio) of 0.16-0.5.

Abstract: Disclosed herein is superparamagnetic fine particles of iron oxide having an unsaturated fatty acid adsorbed on the surface of superparamagnetic fine particles, and having a magnetization of not less than 50 emu/g, the rate of change of the magnetization of not more than 10%, and an Fe.sup.2+ content (calculated as Fe.sup.2+ /Fe.sup.3+ molar ratio) of 0.16-0.5.

Abstract: Disclosed herein are polydiphenyldiacetylenes having the following repeating unit (III): ##STR1## (wherein R.sup.1 denotes a hydrogen atom or a methoxy group; R.sup.2 denotes a hydrogen atom, a methoxy group or a methylamino group; R.sup.3 denotes a hydrogen atom or a trifluoromethyl group; and R.sup.4 denotes a hydrogen atom or a trifluoromethyl group; provided that R.sup.1 is not a hydrogen atom when R.sup.2 is hydrogen atom, and R.sup.3 is not a hydrogen atom when R.sup.4 is hydrogen atom).

Abstract: Disclosed herein is a coating composition comprising plate-like iron oxide particles having an average particle diameter of 4 to 25 .mu.m, a lamellar thickness of 0.16 to 5 .mu.m and a plate ratio (average particle diameter:lamellar thickness) of 5:1 to 25:1, at least one pigment selected from the group consisting of a coloring pigment,a mica pigment and a metal powder pigment, a film-forming polymer, and an organic solvent.

Abstract: Disclosed herein is a method for bonding a resin part, which comprises disposing a magnetic complex composed of a resin and magnetic particles as a heating-medium at the resin parts to be bonded, and applying an alternating magnetic field to the heating-medium by using a magnetic field generating means composed of an electromagnetic core and an exciting coil, thereby making said heating-medium generate heat for fuse-bonding said resins.

Abstract: Disclosed herein is a coating composition comprising plate-like iron oxide particles having an average particle diameter of 0.5 to 5.0 .mu.m, a lamellar thickness of 50 to 500.ANG. and a plate ratio (the ratio of the average particle diameter to the lamellar thickness) of 50:1 to 500:1, at least one pigment selected from the group consisting of a coloring pigment, a mica pigment and a metal powder pigment, a film-forming polymer, and an organic solvent.

Abstract: Composite magnetic compacts having good conductivity and excellent mechanical and magnetic properties and their forming methods. The composite magnetic compacts are basically made by forming mixtures consisting essentially of 1 to 50 percent by weight of a magnetic powder and the remaining percentage of a powder of superplastic Zn-22Al alloy. A drop in the strength of the compacts that occurs when the mixing percentage of the magnetic powder increases is made up for by the impregration of plastic in the compacts or the simpler addition of a plastic powder to the mixture of the powders of magnetic material and superplastic Zn-22Al alloy. The forming methods of the composite magnetic compacts are carried out at different temperatures and under different conditions depending on the composition of the powder mixtures and so on.

Abstract: Disclosed herein are sphere-like magnetite particles showing an apparent density of from 0.40 to 1.00 g/cm.sup.3 and a high thermo-stability and containing from 0.1 to 5.0 atomic % of Si to Fe, and a process for producing the sphere-like magnetite particles.

Abstract: To obtain an anticorrosive Fe-B-R type permanent magnet; in particular, to reduce deterioration rate of the initial magnetic properties below 10% after the magnet has been kept at 80.degree. C. in 90% relative humidity for 500 hours, the surface of the sintered permanent magnet is coated with metallic coating film layers of at least one noble metal layer and at least one base metal layer disposed on the noble metal layer. Diffusion heat treatment further improves the adhesiveness of the coating film layers.

Abstract: A corrosion-resistant R-Fe-B type sintered permanent magnet exhibiting deterioration of not more than 5 % from the initial magnetic properties after being tested for 500 hours under the conditions of a temperature of 80.degree. C. and a relative humidity of 90 % is produced by:causing at least one colloidal noble metal selected from the group consisting of Pd, Ag, Pt and Au to be adsorbed in a colloidal state or forming a thin layer thereof through vapor deposition on the surface of the sintered body; applying at least one base metal selected from the group consisting of Ni, Cu, Sn and Co containing P and/or B by electroless plating; and further applying at least one base metal selected from the same group.The noble metal layer is 1-10 nm thick. The electroless plating layer is no more than 10 .mu.m and the electrolytic plating layer 5-60 .mu.m thick.