238results about How to "Fast dissolution rate" patented technology

The invention relates to a complex heavy-metal waste water emergency quick treatment method, comprising the following steps of: filtering by a sand filter; mixing by a high-speed pump; carrying out an ultraviolet catalyzing ozone reaction; carrying a microwave catalyzing active carbon reaction; carrying micro-electrolytic reaction; circulating waste water; carrying out a Fenton reaction; carryingout electric flocculation on an aluminum electrode plate; and pressing and filtering sludge. Waster water in a circulating slot is pumped into an iron carbon fluidized bed by a fluidizing pump to be circularly treated; an air compressor is connected with the iron carbon fluidized bed and prevents a filler in the iron carbon fluidized bed from blocking; and the microwave active carbon reactor is an active carbon filling tower, and a microwave emitter is arranged outside the body of the active carbon filling tower. The complex heavy-metal waste water emergency quick treatment method disclosed by the invention is used for treating the complex heavy-metal waste water, associated devices are simple, easy, quick, can meet an emergency, and can update and convert, no various chemical raw materials are fed, and various complex heavy-metal waste water with unknown elements can be quickly treated as long as the current magnitude is regulated, and thus the heavy metal in the waste water and chemical oxygen demand can immediately reach the standard and are discharged.

The invention relates to a double-sided photo-thermal conversion material and a solar seawater evaporation device constructed by the same. The double-sided photo-thermal conversion material has a composite layer (more than two layers) structure, and the upper and lower layers are hydrophilic photo-thermal conversion materials. The device is composed of the double-sided photo-thermal conversion material (with a three-layer composite structure, the lower layer is completely immersed in seawater, and the upper layer is located above the water surface), a water tank (containing seawater), a waterlevel adjusting mechanism (capable of adjusting the height of the water surface) and a turnover mechanism (capable of intermittently driving the double-sided material to turn over up and down). Alternatively, the device is composed of a conveyor belt (which is a hydrophilic photo-thermal conversion material with a double-layer composite structure and is distributed into three parts, namely, a partbelow the water surface, a part above the water surface and a part outside the water tank), a water tank, a water level adjusting mechanism, a supporting mechanism (capable of supporting the conveyorbelt) and a driving mechanism (capable of continuously driving the conveyor belt to work). The problems that in the prior art, salt particles separated out of the surface of a hot layer are not removed in time, consumed time is long, and cost is high are effectively solved.

The invention discloses aspirin pulsed release pellets, its preparation and a preparation method thereof. The pellets comprise blank pellets, an aspirin-containing drug layer, an isolation layer, a regulation releasing layer and a protective layer. The regulation releasing layer contains polyprotic acid and/or its salt, anionic polymer salt, a plasticizer and an antiadherent. The anionic polymer salt is prepared by the following method: dissolving an enteric material, and using alkali to neutralize to a pH value greater than the enteric material dissolution pH value 0.1-3. The protective layer contains the enteric material, the plasticizer and the antiadherent. The enteric material is any one material selected from: an enteric material dissolved at pH value of 4.5-5.5 to prepare pellets I; an enteric material dissolved at pH value of 6.0-6.5 to prepare pellets II; or an enteric material dissolved at pH value of 7.0-8.0 to prepare pellets III. According to the preparation, local drug concentration will not be high, accumulation of the drug inside the body can be reduced, patient compliance can be improved, and stability inside the body can be raised. Therefore, bioavailability and the antithrombotic effect are raised.

The invention relates to a maca teabag and a preparation method thereof. The maca teabag is prepared from the raw materials of 10-15 parts of maca, 5-8 parts of raspberries, 3-6 parts of barley, 2-4 parts of osmanthus fragrans and 1-3 part(s) of Pu-Er ripe tea through the steps of raw material selecting, smashing, screening with a vibrating screen, weighting, component mixing and final subpackage. The maca teabag is reasonable in components and ratio design, and rich in nutrition, and the effects of all components are supplementary to one another; the preparation method is simple and convenient, and the cost is low; the maca teabag is prepared from natural components completely, so that original taste and flavour are kept, the tea soup of the maca teabag is brownish yellow, strong in wheat flavor and flower fragrance, and mellow in taste; the dissolution rate is high, extract is multiple, brewing resistance is achieved, maca teabag is carried and drunk conveniently by people, and a new beverage with the efficacities of tonifying kidney, building body and resisting fatigue is provided.

The invention relates to an Entecavir tablet. The Entecavir tablet contains 0.2-1% of Entecavir monohydrate, 85-98% of filler, 0-5% of binder, 0-10% of disintegrating agent, 0-2% of flow aid and 0.5-2% of lubricating agent by weight, wherein the Entecavir monohydrate is added in the form of powder. The invention also relates to a preparation method of the Entecavir tablet.

The present invention relates to an olanzapine oral disintegration tablet and a preparation method thereof. The olanzapine oral disintegration tablet comprises: olanzapine, mannitol, and calcium hydrogen phosphate. The olanzapine oral disintegration tablet uses the olanzapine as the raw material, comprises one or more pharmaceutically acceptable excipients and is prepared by a direct compression. The olanzapine oral disintegration tablet can be quickly disintegrated in vitro, and quickly and uniformly disintegrated and dispersed, and is slightly sweet and tastes good. The olanzapine oral disintegration tablet is conveniently taken, and is especially suitable for the patients with emergency in dysphagia or special environment such as the elderly, children, and coma patient. The olanzapine oral disintegration tablet has the advantages of simple preparation process and low cost, and is suitable for industrialized production.

The invention relates to the field of medicament preparation, in particular to a lansoprazole enteric preparation and a preparation method thereof. A lansoprazole enteric pellet is provided with an empty pellet core, a medicament layer, an isolation layer and an enteric coating layer in turn from the interior to the exterior, wherein the medicament layer contains lansoprazole, disintegrating agent, compatibilizer and basic stabilizing agent; and the lansoprazole enteric preparation is characterized in that the medicament layer also comprises micronized crosslinked povidone. The lansoprazole enteric preparation and the preparation method thereof have the advantages of higher dissolution rate of enteric pellets, reducing consumption and variety of compatibilizer, saving the preparation cost, reducing the technical difficulty and contributing to human safety.

The invention belongs to the technical field of medicines and particularly relates to a ropivacaine mesylate compound. The structural formula of the ropivacaine mesylate compound is shown in the description, and an X-ray powder diffraction spectrogram obtained by measuring the ropivacaine mesylate compound with Cu-K alpha rays is shown in figure 1. The invention also provides a preparation process of the ropivacaine mesylate compound, a pharmaceutical composition containing the ropivacaine mesylate compound and a preparation process of the pharmaceutical composition. Dosage forms of the ropivacaine mesylate pharmaceutical composition are powder injections, small volume injections and large volume injections. The ropivacaine mesylate compound is high in solubility and high in dissolution rate, and the pharmaceutical composition of the ropivacaine mesylate compound is good in dissolubility, easy to dissolve and composite and high in bioavailability.

The invention provides an antineoplastic compound deacetylase fungus epoxy ethyl ester injection and a preparation method thereof, belonging to a compound. The antineoplastic compound deacetylase fungus epoxy ethyl ester injection can solve the slightly solubility problem of deacetylase fungus epoxy ethyl ester, can increase the oral bioavailability of deacetylase fungus epoxy ethyl ester and hasgood stability. The antineoplastic compound deacetylase fungus epoxy ethyl ester injection is nano suspension freeze-dried powder and comprises deacetylase fungus epoxy ethyl ester, a surface active agent, a suspending agent and a freeze-drying protecting agent in the mass ratio of 1:(0.5-10):(0-10):(2-10). The preparation method comprises the following steps of: putting deacetylase fungus epoxy ethyl ester, the surface active agent and the suspending agent in a container, adding water, predispersing, homogenizing, adding the freeze-drying protecting agent, dissolving by stirring, subpackaging, freezing, and freeze-drying to obtain the antineoplastic compound deacetylase fungus epoxy ethyl ester injection.

The invention provides a codonopsis pilosula, poria cocos and white atractylodes rhizome tea bag which is prepared from the following substances in parts by mass: 15 to 30 parts of codonopsis pilosula, 15 to 30 parts of poria cocos, 15 to 25 parts of white atractylodes rhizome, 10 to 18 parts of hawthorns, 10 to 18 parts of semen cassia, 8 to 15 parts of white chrysanthemum flowers, 8 to 15 parts of momordica grosvenori, 8 to 15 parts of rose flowers, 6 to 12 parts of orange peels and 6 to 10 parts of tea leaves. The invention further provides a preparation method of the codonopsis pilosula, poria cocos and white atractylodes rhizome tea bag. The codonopsis pilosula, poria cocos and white atractylodes rhizome tea bag disclosed by the invention has the effects of tonifying qi, strengthening the spleen, promoting digestion to eliminate stagnation, relaxing bowel, reducing lipid and pressure, reducing fat, losing weight, reducing blood fat, preventing and treating thrombus and regulating the physiological function of a human body, further has the effects of protecting the health and nourishing the life, and is a safe and toxic and side effect-free natural blood fat and blood pressure reducing good product.

The invention discloses a method for producing battery-grade nickel sulfate by taking nickel oxide as a raw material. The method is characterized by comprising the following steps: (1) pretreating nickel oxide by using sulfuric acid with a hydrogen ion concentration of 8-12 mol/L, carrying out solid-liquid separation, carrying out solid-liquid separation by using sulfuric acid with a hydrogen ionconcentration of 3-6 mol/L to obtain a solid, filtering the obtained solution to obtain a filtrate; and (2) neutralizing the filtrate obtained in the step (1) by using nickel carbonate, evaporating the obtained solution, and carrying out crystallization and drying to obtain the battery-grade nickel sulfate product. According to the method, the dissolution rate of nickel oxide is increased by aboutone time, purification and impurity removal are not needed, and a nickel sulfate product can be produced by directly carrying out evaporative crystallization. A crystallization mother liquid can be repeatedly used, resources are saved, the extraction process is short, and cost is low.

The invention belongs to the technical field of production of fluid ores of petroleum, natural gas, shale gas and the like, and particularly discloses a preparation technology of a self-suspension coated support material. The preparation technology comprises the following steps: (1) heating aggregate to the temperature of 80 to 230 DEG C, and stirring and mixing the heated aggregate; (2) cooling to the temperature of 75 to 200 DEG C, adding inner resin and a curing agent of the inner resin, and stirring, thus forming an inner coating layer; (3) cooling to the temperature of 65 to 190 DEG C, adding a drag reducer, and stirring; (4) cooling to the temperature of 55 to 130 DEG C, adding a catalyst, outer resin, an amine additive and a curing agent of the outer resin, and stirring, thus forming an outer coating layer; (5) cooling to the temperature of 40 to 80 DEG C, adding a blocking agent, and stirring; (6) cooling to the temperature of 30 to 70 DEG C, discharging out of a pot, and controlling the apparent density of a low-density support agent within the range of 1.05 to 2.60g/cm<3>. The self-suspension coated support material prepared by the preparation technology has the advantages that the flow guide property is good, the self-suspension property is good, and the friction drag is low.

The invention discloses a fertilizer for the flowering and fruiting period of wolfberry, relates to the technical field of fertilizers for soil testing and formulated fertilization and particularly relates to a special water-soluble fertilizer for the flowering and fruiting period of wolfberry. The water-soluble fertilizer contains more than or equal to 50wt% of effective elements including N, P2O5 and K2O, more than or equal to 0.4wt% of microelements and 0.05-0.10wt% of a plant growth regulator, wherein the effective elements include 18.0-23.0wt% of N, 10.0-15.0wt% of P2O5 and 20.0-25.0wt% of K2O; and the microelements include 0.1-0.5wt% of B, 0.1-0.5wt% of Fe, 0.1-0.5wt% of Zn and 0.1-0.5wt% of Mo. The fertilizer disclosed by the invention is prepared by mixing nutrients including macroelements, medium elements, microelements and the like and the plant growth regulator at a proper ratio according to the soil nutrient supply characteristic of Qaidam Basin and the nutrient demand characteristic of the flowering and fruiting period of wolfberry so as to have the characteristics of high concentration, good water solubility, nutrient completeness and high utilization ratio; due to the application of the fertilizer, the requirements for a great deal of N and K in the flowering and fruiting period of wolfberry are met, and therefore, the aims of increasing the yield of wolfberry and improving the quality are achieved. The fertilizer can be applied to wolfberry fertilization along with water under a drip irrigation condition.

The invention provides a medicine composition for Jardiance solid dispersion and a preparation method thereof. The method comprises the steps that Jardiance and polyethylene glycol are prepared into the solid dispersion in a melting mode, and the solid dispersion is mixed with other pharmaceutically acceptable excipients to form the oral solid preparation. According to the medicine composition, the main medicine solubility is improved, rapid medicine disintegration is facilitated, and therefore the composition dissolution speed is increased.

The invention discloses a berberine hydrochloride caffeic acid eutectic compound, a preparation method thereof, a composition of the berberine hydrochloride caffeic acid eutectic compound, and applications, and more specifically, discloses a novel berberine hydrochloride caffeic acid eutectic compound taking berberine hydrochloride as a medicinal active component and caffeic acid as an eutectic precursor, a preparation method of the berberine hydrochloride caffeic acid eutectic compound, and applications of the berberine hydrochloride caffeic acid eutectic compound as a medicinal active component in preparation of medicines used for preventing and treating cardiovascular diseases, preventing virus, treating cancers, reducing blood fat, reducing blood sugar, preventing inflammation, preventing bacteria, and preventing infection.