Abstract: Controlled height carbon nanotube arrays including catalysts and synthesis methods relating thereto are disclosed. Such nanotube arrays can be prepared from catalyst particles having an Fe:Co:Ni molar ratio impregnated in an exfoliated layered mineral to grow carbon nanotube arrays where the Fe:Co:Ni molar ratio of the catalyst is used to control the height of the array.

Abstract: A titanium-containing calcium hexaaluminate material and preparation method thereof is disclosed. The technical solution is: using 60˜80 wt % alumina micro powder, 5˜20 wt % calcium-containing micro powder, 10˜20 wt % titania micro powder and 1˜10 wt % manganese oxide micro powder as raw materials, blending the raw materials evenly in a planetary ball mill to obtain a blend, machine pressing the blend at 100˜200 MPa to obtain a green body, drying the green body at 110˜200° C. for 12˜36 h, and incubating the dried green body at 1500˜1800° C. for 1˜8 h to obtain the titanium-containing calcium hexaaluminate material. The present disclosure has low cost and simple process, and the prepared titanium-containing calcium hexaaluminate material has the characteristics of good chemical stability, high thermal shock resistance and strong melt resistance to titanium-aluminum alloy.

Abstract: The present disclosure relates to a magnesium-based raw material and a preparation method thereof. According to the technical solution, 40-60 wt % fused magnesia particles, 30-40 wt % fine monoclinic zirconia powder, 5-20 wt % fine zirconium oxychloride powder, 0.5-1.5 wt % calcium hydroxide nanopowder, 0.2-0.5 wt % calcium hydroxide nanopowder, and 0.1-0.3 wt % maleic acid are stirred for 15 min to mix well in a high-speed mixing mill at a constant temperature of 25° C. to obtain a mixed powder; and the mixed powder is mixed through a ball mill at a constant temperature of 25° C. for 3 min, roasted in a high temperature furnace at 250-400° C. for 0.5-3 h, and finally cooled to room temperature.

Abstract: The invention relates to the technical field of lithium battery slurry materials, in particular to a conductive carbon material dispersing agent which comprises one of modified polyvinyl alcohol, alkyl ammonium salt copolymer, olefin block maleic anhydride copolymer and pyrrolidone copolymer, or mixtures thereof, and can effectively disperse carbon nanotube, graphene and other conductive carbon materials in a solvent to obtain uniform conductive slurry; further disclosed is a high-conductivity slurry for the lithium battery, which comprises 0.5-15.0% by weight of a conductive carbon material and 0.1-3.0% by weight of a dispersing agent, and can remarkably reduce the bulk resistivity of a positive electrode system of the lithium battery and improve the conductivity of a pole piece.

Abstract: The present disclosure provides a method for determining free radicals of CaO—Al2O3 series oxide melts. The method includes dividing the CaO—Al2O3 series oxide powder to into two aliquots by mass, putting into two identical corundum crucibles and tamping. The method also includes heating the two aliquots at the same high temperature in furnaces with and without a static magnetic field, respectively. Cylindrical samples with the same diameter and height, and only containing the melt at the bottom of the crucible and the slag reaction interface are drilled out from said two crucibles and ground into powder samples. The free radical relative content of the CaO—Al2O3 series oxide melts can be calculated from a ratio between the difference of the reaction mass contents of CaO in the two powder samples and the total mass content of CaO.

Abstract: The present disclosure relates to a magnesium-based raw material with low thermal conductivity and low thermal expansion and a preparation method thereof. According to the technical solution, 40-60 wt % fused magnesia particles, 30-40 wt % fine monoclinic zirconia powder, 5-20 wt % fine zirconium oxychloride powder, 0.5-1.5 wt % calcium hydroxide nanopowder, 0.2-0.5 wt % calcium hydroxide nanopowder, and 0.1-0.3 wt % maleic acid are stirred for 15 min to mix well in a high-speed mixing mill at a constant temperature of 25° C. to obtain a mixed powder; and the mixed powder is mixed through a ball mill at a constant temperature of 25° C. for 3 min, roasted in a high temperature furnace at 250-400° C. for 0.5-3 h, and finally cooled to room temperature. The magnesium-based refractory material prepared has the advantages of relatively low thermal conductivity, low thermal expansion coefficient, excellent dispersibility, and strong resistance to slag penetration and erosion.

Abstract: The disclosure relates to a phase change thermal storage ceramic having high service temperature and improved utilization rate and utilization efficiency of heat. It is prepared at a low cost with a simple, easy-to-industrially-realized method. A mixture is obtained by mixing and stirring evenly 50-85 wt % of fused mullite powder, 10-45 wt % of pretreated aluminum-silicon alloy powder, and 3-8 wt % of ball clay. A ceramic body is formed by press molding the mixture at 80-150 MPa. The ceramic body is cured at 25-28° C. and a relative humidity of 70-75 RH for 24-36 h, dried at 80-120° C. for 24-36 h, and held at 1,100-1,300° C. for 3-5 h to prepare the phase change thermal storage ceramic. The pretreated aluminum-silicon alloy powder is prepared by holding aluminum-silicon alloy powder in water vapor at 0.02-0.20 MPa for 0.5-3 h to impregnate in an alkaline silica sol and drying the impregnated powder.

Abstract: A titanium-containing calcium hexaaluminate material and preparation method thereof is disclosed. The technical solution is: using 60˜80 wt % alumina micro powder, 5˜20 wt % calcium-containing micro powder, 10˜20 wt % titania micro powder and 1˜10 wt % manganese oxide micro powder as raw materials, blending the raw materials evenly in a planetary ball mill to obtain a blend, machine pressing the blend at 100˜200 MPa to obtain a green body, drying the green body at 110˜200° C. for 12˜36 h, and incubating the dried green body at 1500˜1800° C. for 1˜8 h to obtain the titanium-containing calcium hexaaluminate material. The present disclosure has low cost and simple process, and the prepared titanium-containing calcium hexaaluminate material has the characteristics of good chemical stability, high thermal shock resistance and strong melt resistance to titanium-aluminum alloy.

Abstract: A double-shell phase change heat storage balls and preparation method thereof is disclosed. The technical scheme is as follows. Paraffin is placed in oven, and organic ignition loss is added to obtain paraffin melt containing the ignition loss; metal balls is immersed in the paraffin melt containing the ignition loss, and cooled naturally to obtain the metal balls coated by ignition loss and paraffin; alumina refractory slurry is placed in a pan granulator, and the metal balls coated by ignition loss and paraffin is added, pelletized, and dried to obtain alumina composite phase change heat storage ball bodies; mullite refractory slurry is placed in a pan granulator, alumina composite phase change heat storage ball bodies is added, pelletized, dried, and placed in a muffle furnace. The temperature is raised to 1200-1600° C. by three systems and maintained. After naturally cooling, the double-shell phase change heat storage balls are prepared.

Abstract: Controlled height carbon nanotube arrays including catalysts and synthesis methods relating thereto are disclosed. Such nanotube arrays can be prepared from catalyst particles having an Fe:Co:Ni molar ratio impregnated in an exfoliated layered mineral to grow carbon nanotube arrays where the Fe:Co:Ni molar ratio of the catalyst is used to control the height of the array.

Abstract: The invention relates to the technical field of lithium battery slurry materials, in particular to a conductive carbon material dispersing agent which comprises one of modified polyvinyl alcohol, alkyl ammonium salt copolymer, olefin block maleic anhydride copolymer and pyrrolidone copolymer, or mixtures thereof, and can effectively disperse carbon nanotube, graphene and other conductive carbon materials in a solvent to obtain uniform conductive slurry; further disclosed is a high-conductivity slurry for the lithium battery, which comprises 0.5-15.0% by weight of a conductive carbon material and 0.1-3.0% by weight of a dispersing agent, and can remarkably reduce the bulk resistivity of a positive electrode system of the lithium battery and improve the conductivity of a pole piece.

Abstract: A lightweight micro-closed-pore corundum composite refractory and a method preparing the same, wherein raw materials of the refractory comprise 95-99 parts by weight of ?-Al2O3 micro-powder and 1-5 parts by weight of dolomite clinker; and additives of the refractory comprise 2-15 parts by weight of nano alumina sol, 5-15 parts by weight of a carbohydrate polymer, and 30-50 parts by weight of an organic alcohol. and the lightweight micro-closed-pore corundum composite refractory is prepared by: mixing and wet grinding the raw materials and the additives to obtain a slurry; placing the slurry in a mold, keeping the mold at 15-25° C. for 6-12 hours and then keeping the mold at 60-90° C. for 6-12 hours, then demolding; drying a demolded green body at 110-200° C. for 24-36 hours, and keeping the green body at 1800-2000° C. for 2-5 hours. A method preparing a lightweight micro-closed-pore corundum composite refractory is also provided.

Abstract: A lightweight micro-closed-pore corundum composite refractory and a method preparing the same, wherein raw materials of the refractory comprise 95-99 parts by weight of ?-Al2O3 micro-powder and 1-5 parts by weight of dolomite clinker; and additives of the refractory comprise 2-15 parts by weight of nano alumina sol, 5-15 parts by weight of a carbohydrate polymer, and 30-50 parts by weight of an organic alcohol. and the lightweight micro-closed-pore corundum composite refractory is prepared by: mixing and wet grinding the raw materials and the additives to obtain a slurry; placing the slurry in a mold, keeping the mold at 15-25° C. for 6-12 hours and then keeping the mold at 60-90° C. for 6-12 hours, then demolding; drying a demolded green body at 110-200° C. for 24-36 hours, and keeping the green body at 1800-2000° C. for 2-5 hours. A method preparing a lightweight micro-closed-pore corundum composite refractory is also provided.

Abstract: A thermally conductive structure and a heat dissipation device are provided. The thermally conductive structure comprises a first thermally conductive layer and a second thermally conductive layer. The first thermally conductive layer comprises a graphene material and first carbon nanotubes, and the first carbon nanotubes are dispersed in the graphene material. The second thermally conductive layer is stacked on the first thermally conductive layer, and comprises a porous material and second carbon nanotubes, and the second carbon nanotubes are dispersed in the porous material. The heat dissipation device comprises the thermally conductive structure and a heat dissipation structure. The thermally conductive structure is in contact with a heat source, and the heat dissipation structure is connected to the thermally conductive structure.

Abstract: The loss in delivered capacity (capacity fade) after cycling non-aqueous rechargeable lithium manganese oxide batteries at elevated temperatures can be greatly reduced by depositing a small amount of certain foreign metal species on the surface of spinel in the cathode. In particular the foreign metal species are from compounds having either bismuth, lead, lanthanum, barium, zirconium, yttrium, strontium, zinc or magnesium. The foreign metal species are introduced to the surface of spinel by moderately heating either an aqueous treated mixture or a dry mixture of ready-made spinel and the foreign metal compound.

Abstract: The loss in delivered capacity (fade) after cycling non-aqueous rechargeable lithium batteries can be reduced by incorporating a cathode powder that has been mixed and heat-treated with a small amount of lithium borate. The invention is particularly suited to lithium ion batteries.

Abstract: The loss in delivered capacity (fade) after cycling non-aqueous rechargeable lithium batteries can be reduced by incorporating a cathode powder with LiCoO2type-structure that has been mixed and heat-treated with a small amount of lithium borate. The invention is particularly suited to lithium ion batteries.

Abstract: The loss in delivered capacity (fade rate) after cycling non-aqueous rechargeable lithium batteries can be reduced by incorporating a small amount of an improved additive in the battery. Improved additives include boron trifluoride (BF.sub.3), fluoboric acid (HBF.sub.4), or complexes thereof. The invention is particularly suited to lithium ion batteries. Complexes comprising BF.sub.3 and dietyl carbonate or ethyl methyl carbonate can be prepared which are particularly effective additives. Preferably, the additive is dissolved in the electrolyte.