3242results about How to "Small particles" patented technology

A novel dosage form. The dosage form is presented in particulate form and before oral ingestion the particulate material is subjected to an aqueous medium, whereby it is converted to a semi-solid form by swelling or gelling of one or more of the components, especially of a gellan gum, of the particulate matter. The invention also relates to a vehicle for oral administration of one or more active substances, the vehicle comprising a gellan gum arranged in a configuration allowing optimal water diffusion so that upon addition of a predetermined amount of an aqueous medium, without the necessity of applying shear forces or other mixing forces, within a time period of 5 minutes or less swells and/or gels and the texture of the swelled vehicle being similar to that of a soft pudding and having a viscosity of at least about 10,000 cps as measured by a Brookfield Viscometer with a #4 LV spindle at 6 rpm and at 20-25° C. In one embodiment of the invention, the particulate matter can be moulded into a desired shape or pressed onto a dispensing unit such as a spoon.

The invention relates to a nanoscale lithium titanate compound and a preparation method thereof. The nanoscale lithium titanate compound is prepared by following steps: a lithium compound, a titanium compound and a doped element compound are mixed according to a molar ratio of 0.75-0.80:1:0:0.05 of Li to Ti to doped elements so as to form a mixture A; the mixture A and a complexing agent are mixed according to a weight ratio of 1:0.1-10 and dissolved in water to form a mixture B; and the mixture B and a carbon nanotube dispersion C are mixed to form the nanoscale lithium titanate compound coated by carbon nanotubes with a nanoscale grain size. The preparation method comprises the following steps: mixing the mixture B and the carbon nanotube dispersion C; heating an obtained mixture in nitrogen at 100-200 DEG C for 1-2 hours to obtain gel; and sintering the obtained gel in inert atmosphere at 500-1,000 DEG C for 5-48 hours to obtain the powdered lithium titanate compound. The lithium titanate compound is nanoscale lithium titanate coated by the carbon nanotubes, has fine and even grain and high purity and has the characteristics of higher charge and discharge capacity, good rate discharge performance, good cycle performance and good safety performance, and the like, thus the lithium titanate compound is an ideal anode material for manufacturing a lithium ion battery.

The invention provides a preparation method for small-size ZSM-5 molecular sieve. Wherein, using pearlite and montmorillonite as material for aluminum, adding crystal seed for crystallization reaction on hydrothermal condition, and obtaining a small-size product with 5~95% ZSM-5 that can be used to prepare modified ZSM-5 molecular sieve by different post-treatment method or as the active intergradient or carrier for catalyst. This invention cuts the cost more.

This invention discloses a method for preparing neutral titanium dioxide nanosol. The method comprises: (1) preparing amorphous titanium dioxide; (2) dispersing and dissolving amorphous titanium dioxide; (3) performing hydrothermal treatment to obtain neutral titanium dioxide nanosol. The obtained neutral titanium dioxide nanosol (below 10 nm) is transparent and golden, and does not have any odor. Besides, the neutral titanium dioxide nanosol has such advantages as high stability, certain crystallinity, high specific surface area, high adhesiveness, reduced particle sizes after doped with transition metal, and high utility of visible light. The method has such advantages as wide raw materials and easy operation, and is suitable for large-scale production.

The invention provides a preparation and application method for photocatalysis environmental protection type painting, which relates to construction painting, especially provides a preparation and application method for photocatalysis function painting, which includes steps: mixing titanium-containing organic, water, chelating agent and hydrolysis inhibitor to prepare nano anatase type titanium dioxide water sol; adding metal, oxide or impure titanium dioxide photocatalyst into the titanium dioxide water sol and stirring equably. Using method is coating inorganic isolated layer firstly and coating the photocatalysis painting after drying. Advantages of the invention are: the prepared painting and using technique can be widely used for inner and outer wall surface of building and is harmless to bottom ainting, photocatalysis efficiency is high, cost is low, bonding is firm, transparency is good, preparation is simple, and usage is easy.

The invention relates to the technical field of lithium-ion cathode material, in particular to silicon cathode material coated with graphene and a preparation method of the silicon cathode material coated with the grapheme. The preparation method comprises the following steps: A, preparing oxidized graphene suspension liquid; B, preparing nanometer silicon particle suspension liquid; and C, preparing silicon cathode material coated with grapheme. The preparation method adopts the electrostatic self-assembly synthetic technology and is wide in source of raw material, low in price, simple in synthetic method, easy for control of process conditions, strong in operability and good in repeatability. The silicon cathode material coated with grapheme is high in specific capacity and good in cycle performance and rate capability, wherein the specific discharge capacity for the first time under the electric current density of 0.01-1.2V, 200mA/g can reach 2746mAh/g, and the specific discharge capacity after 100 times of cycles can maintain 803.8mAh/g.

The invention discloses a high-efficiency feed crushing and vibrating screening device, which comprises a base, a slide rail is fixed on the top of the base through a bracket, a crushing box is slidably connected above the slide rail, a screen is arranged at the bottom of the crushing box, and a bottom left corner of the crushing box is connected with a Moving rod; the top of the base is also provided with a fixed seat, the front side wall of the fixed seat is provided with a deceleration motor, the motor shaft at the front end of the deceleration motor is installed with a rotating disc, the top of the front end of the rotating disc is provided with a pin shaft, and the pin shaft is rotatably connected with a connecting rod , the connecting rod is hinged with the moving rod; the left end of the slide rail is fixedly provided with a fixed rod, the top of the front side wall of the fixed rod is hinged with a knocking rod, the bottom of the knocking rod is fixedly provided with a baffle, and the top of the moving rod is provided with a push plate. During the feed grinding process of the present invention, the grinding box moves left and right by rotating the disc, thereby driving the feed to shake; during the grinding process, the knocking rod knocks on the side wall of the grinding box to prevent the feed from sticking to the inner wall of the grinding bucket and avoid screen blockage.

A three-element catalyst for cleaning the tail gas of car features that the cellular cordierite ceramics modified by the RE tailing mixture or transition metal oxide is ued as the first carrier, the internal and external modified alumina coating layers are used as the second carrier, and the noble metal Pt, Rh or Pd is used as its active component.

The invention discloses a method for preparation of biochar from banana peel. The method comprises the steps of: (1) crushing banana peel, then mixing the crushed banana peel with an aqueous solution of an activator, and performing standing; then carrying out washing and drying to obtain a biochar precursor, wherein the activator is at least one of alkali metal hydroxide, lewis acid and peroxide; (2) mixing the biochar precursor with an acid solution, then carrying out hydrothermal charring reaction at 180DEG C-260DEG C, and at the end of the hydrothermal charring reaction, carrying out washing and drying to obtain the biochar. In addition, the invention also comprises the biochar prepared by the method and application of the biochar to adsorption of heavy metals. The method provided by the invention utilizes agricultural production waste to prepare a biochar adsorbent by simple and rapid hydrothermal charring method, turns waste into treasure, makes full use of resources, reduces environmental pollution, has good economic benefits, develops new technology, and is beneficial to industrial production.

The present invention pertains to the technical field of the preparation of surface metallized composite material and relates to a preparation method of surface metallized composite material through chemical plating under photocatalysis, wherein the fibre, plastic, fabric, resin, glass, ceramic, monocrystalline silicon or metal encapsulated with semiconductor nano inorganic powder is used as substrate material, or the semiconductor nano inorganic powder is used as substrate material, the photocatalytic technique integrates the reducer effect in conventional chemical plating, metal is carried on the surface of substrate material effectively, and surface metallized composite material is prepared. The advantage is that it makes use of the feature that semiconductor nano inorganic powder will be excited and generate a large number of electron-cavity pairs under the irradiation of photons of which energy is equal to or greater than band-gap energy, while electrons have a reducing effect and help accelerate the reduction of metal ions, and combines this feature with the reducer effect in conventional chemical plating to raise plating speed and production efficiency, reduce product cost and prepare surface metallized composite material with uniform surface metal layer, tiny metal particles, high quality and low cost.

The invention relates to a core-shell structure cobalt-base catalyst of a middle distillate for synthesis gas preparation, which comprises the following components in percentage by weight: 5 to 30 percent of cobalt and 70 to 95 percent of silica. The catalyst has the following physical properties: the specific surface area is 200 to 1400m<2>/g, the pore volume is 0.5 to 1.3cm<3>/g, the average pore size is 2.0 to 18nm, the cobalt crystallite dimension is 12 to 25nm, and the particle size of the core-shell structure cobalt-base catalyst is less than 100nm, and cobaltosic oxide nano particles are coated in a mesoporous silicon shell to form a core-shell structure. The invention has the advantages of simple operation, high yield, high activity and high selectivity of the middle distillate.

The present invention relates to pharmaceutical compositions comprising a pharmaceutically acceptable salt of caspofungin as active ingredient being useful for the prevention and/or treatment of fungal infections. Said compositions additionally comprise specific bulking agents and small amounts or no amounts of an additional pH modifier and may be in a liquid or solid form, e.g. may be lyophilized compositions. Said compositions show good stability and reduced amounts of sub-visible particulate matter formed in solutions which are reconstituted from the lyophilized product.

The invention discloses a preparation method of a mesoporous SiOx/C composite negative material of a lithium-ion battery, and belongs to the fields of new materials and electrochemistry. The preparation method comprises the following steps of: taking polyvinylpyrrolidone as an auxiliary template agent, taking an organic surface active agent as a template agent and organic silicon as a silicon source, obtaining mesoporous silica precursor by hydrothermal treatment, adding a carbon source, and preparing SiOx/C composite negative material with a mesoporous structure by carbothermic reduction reaction occurring in the process of high-temperature thermal treatment. The preparation method disclosed by the invention has the advantages that the specific capacity of the material is high, the structure is novel, and simultaneously the cycling stability is good; the yield is high; and the prepared SiOx/C composite material is fine in particle, uniform in particle size and component distribution, high in specific capacity and good in cycling stability, is an ideal composite negative material of the lithium-ion battery, and can be widely applied in the fields such as various portable electronic equipment, electric vehicles and aerospace.

The invention discloses a preparation method of a superfine nanometer lithium iron phosphate electrode material, comprising the following steps of: firstly, taking an iron source compound and a phosphorus source compound as raw materials to obtain nanometer ferrous phosphate as a precursor; and secondly, using the ferrous phosphate and the lithium source compound to prepare the superfine nano lithium iron phosphate electrode material. The preparation method of ferrous phosphate, disclosed by the invention, has a simple production process; the obtained nanometer ferrous phosphate can be used for preparing the high-purity superfine nanometer lithium iron phosphate; and the ferrous valence state is not changed when the ferrous phosphate is used for preparing the lithium iron phosphate, thus, no carbon source compound or reducing agent needs to to be added to change the iron valence state, and then the carbon-coated lithium iron phosphate or non-carbon-coated lithium iron phosphate can be directly prepared. The nanometer lithium iron phosphate manufactured by the nanometer ferrous phosphate precursor has excellent performance, good discharge capacity and voltage platform performance under high capability and high multiplying power, and long cycle life.

The present invention relates to a metal catalyst synthesizing methylal and methyl formate. In weight percentage of the metal catalyst, the content of vanadium is calculated by the weight of V2O5; the content of titanium is calculated by the weight of TiO2; the weight proportion of the V2O5 and the TiO2 in the catalyst is 5 to 70 to 30 to 95; the V2O5 and the TiO2 take 20 percent to 100 percent of the catalyst in weight percentage; the content of accessory ingredient is calculated by the content of the oxide of the accessory ingredient and takes 0wt percent to 2.0wt percent of the catalyst in weight percentage; support takes 0wt percent to 78wt percent of catalyst in weight percentage. The catalyst has the advantages of high methanol conversion rate, the high selectivity of the methylal and the methyl formate, the good stability of the catalyst and long life.

The invention discloses a catalyst for carbon dioxide methanation and a preparation method of the catalyst, belonging to the technical field of carbon dioxide methanation. The catalyst for carbon dioxide methanation is composed of a composite carrier and an active ingredient at a ratio of 84-90wt%:10-16wt%, wherein the composite carrier is composed of gamma-Al2O3 and water soluble metal oxide at a mass ratio of 77-86:2-10; and the active ingredient is Ni which exists in the catalyst in a form of NiO. The catalyst is high in activity, low in cost and better in stability, and can be used for carbon dioxide methanation reaction under normal pressure condition.

The invention relates to a preparation method of a non-supported high-activity hydrogenation catalyst. The preparation method of the non-supported high-activity hydrogenation catalyst is characterized by comprising the following steps: preparing an acid solution A containing at least one group VIII metal compound and at least one group VIB metal compound, and an alkali solution B containing at least one silicon source or aluminium source, slowly mixing the two solutions into a sedimentation reactor, carrying out co-precipitation reaction to obtain slurry under the conditions that temperature is 20-120 DEG C and pH value is 7-12, and carrying out ageing, suction filtration, washing, drying, moulding and roasting on the slurry, so that a catalyst with high catalytic performance for hydrogenation reaction of a fixed bed is obtained. The prepared non-supported hydrogenation catalyst has large specific surface area, high pore volume and high hydrogenation activity; meanwhile, the preparation method of the non-supported high-activity hydrogenation catalyst is simple, reaction conditions are mild, and operation is easy and stable, so that the preparation method of the non-supported high-activity hydrogenation catalyst is applicable to industrial batch-type production.