15731 results about "Distilled water" patented technology

A beverage system is created having beverage, with at least one liquid. The beverage is created in a variety, including tea drink, coffee drink, milk drink, yogurt drink, malted drink, roasted cereal grain beverage, roasted nut and seed beverage, roasted bean beverage, distilled water, mineral water, sports drink, fruit juice, vegetable juice, fruit drink, vegetable drink, fruit skin drink, vegetable skin drink, plant drink, soft drink, alcoholic drink, and soup drink. The beverage is also created with or without addition of ingredient, including flavoring ingredient, nutritional ingredient, health ingredient, and other ingredient. The beverage can be served as hot drink, cold drink, cold drink with ice, and warm drink. The beverage can be caffeinated, or non caffeinated; and diet or non diet. The liquid includes water, oil, and alcohol. The beverage system is created in various form, including bubble beverage, instant beverage, and beverage with dissolved gas.

Fabric and textile conditioning compositions containing particular combinations of cationic polymers and anionic surfactants are disclosed. The polymers are soluble or dispersible to at least 0.01% by weight in distilled water at 25° C., are preferably below a particular molecular weight to afford optimal cleaning and conditioning, and must be present in an effective amount to yield a substantial conditioning benefit. A method of conditioning articles using the polymer/surfactant combinations is also disclosed.

The invention relates to an antibacterium nano fiber material and a preparation method thereof; the material comprises polymer superfine fiber and antibacterial agent, and the weight ratio is 60 to 98: 2 to 40; the preparation method comprises the following steps: (1) the antibacterial agent is dissolved in distilled water to prepare solution; the polymer superfine fiber is dissolved in methylene dichloride or chloroform organic solvent, emulsifier is added to be mixed evenly, to obtain solution which is dispersed evenly; (2) the two types of solution are mixed to obtain even water-in-oil W/O latex, and then electrostatic spinning is conducted to the latex, to obtain the antibacterium nano fiber material. The nano fiber material has good ventilation property and filterability, still has bacteriostasis and sterilization functions for a long time after stably releasing the antibacterial agent, has simple preparation method, adopts the biodegradable and bioabsorbable polymer as carrier materials, can be absorbed by the human body after fully releasing, is not left, does not need secondary operation and has no side effect.

The invention relates to a low-temperature smoke denitration SCR (silicon controlled rectifier) catalyst, which comprises a carrier, a manganese oxide, and composite oxide of one or more of Ce, Zr, Ti, Co, Fe and Cu, the mass content of manganese is 0.1-66 percent, and the total mass content of the Ce, Zr, Ti, Co, Fe or/and Cu is 0-50 percent; and glass fiber and/or kieselguhr is used as the carrier, wherein the glass fiber of the carrier is calcined for 2-4 hours at temperature of 400-600 DEG C, then placed in a nitric acid, sulfuric acid or hydrochloric acid solution with mass concentration of 5-40 percent for acidizing for 1-8 hours, washed by distilled water to be neutered, dried at temperature of 80-120 DEG C, and crushed to have the fineness of 20-325 meshes. The catalyst uses the glass fiber and the kieselguhr as the carriers, so that the dispersion effect of nanoparticles and specific surface area of the catalyst are increased, the high adsorptive capacity and strong heat resistance and corrosion resistance capacity are achieved, stronger toxic resistance capacity to sulfur dioxide and stream contained in the smoke is realized, the invention can be used for 10-200 DEG C of low temperature smoke denitration, and has strong water resisting and sulphur toxic resisting capacities.

The present invention relates to a starch composite plant capsule and its preparation method. Said method includes the following steps: uniformly mixing starch or starch composite, dispersing it in distilled water, heating for 15-60 min, at 60-95 deg.c to make starch be fully gelatinated, then adding plasticizer, gel, surfactant, opacifier, edible color matter, preservative, ant-oxidant and enhancer, fully and uniformly mixing them, then decompressing and defoaming, and adopting conventional capsule-forming process to make the obtained colloid liquid into the invented starch composite plant hollow capsule, and its capsule-forming temperature is 40-95 deg.C.

The invention produces polyethylene alcohol hydrogel dressing containing medicine and chitosan with 60Co gamma-radial or high energy electron beam radial cross linking. Additional, adds in some humectant, plasticizer, medicine, the solvent is the secondary distilled water, physiological saline or phosphate neutral buffer liquid. The product can release medicine slowly and has natural amylose chitosan with biology sterilization activity, it has active sterilization function, at the same time, it has high water quantity, and good water reserving performance, the mechanical intensity is moderate, and the light penetration and air penetration are excellent. It can accord the demands for curing each kind of wound. It can used as the permanent dressing for light skin injuries, and it also can be applied to the temporally close of severe skin organization wound or burn wound.

The invention discloses a method and device for utilizing sewage containing ammonia and sodium. The method comprises the steps of deamination reaction, denitrification reaction, gas-liquid separation, triple-effect multistage evaporation, evaprative crystallization and freezing crystallization, electrodialysis and sodium filteration membrane, and concentration of reverse osmosis membrane, so that distilled water and membrane deion pure water are recovered, and the resource utilization of sole sodium chloride and sodium sulfate is realized.

A desalination apparatus capable of obtaining fresh water stably at low cost by utilizing low-temperature waste, wherein the desalination apparatus including a heat exchanger 92 cooperating with an evaporation can 60 so as to subject a low-temperature waste heat 11 and raw water 62 in the evaporation can 60 to heat exchange and generate water vapor 63 in the evaporation can 60; a condenser 98 cooperating with a raw water tank 72 so as to receive the water vapor 63 from the evaporation can 60, cool the water vapor 63 by subjecting the water vapor 63 and raw water 71 in the raw water tank 72 to heat exchange and obtain distilled water 76; a distilled water tank for storing the distilled water 76; vacuum means for evacuating the evaporation can 60 and depressurizing the inside thereof so as to promote generation of water vapor 63 in the evaporation can 60; and raw water supply means for supplying raw water to the evaporation can.

The invention provides an alkali treatment modifying method of a Y-shaped molecular sieve, which comprises the following steps of: beating and uniformly mixing the Y-shaped molecular sieve and a strong alkali aqueous solution according to the mass ratio of the molecular sieve, a strong alkali and distilled water as (0.1-2): (0.05-2): (4-15), and carrying out alkali treatment for 0.1-24 hours at the temperature of 0-120 DEG C; compared with a parent Y-shaped molecular sieve, the obtained molecular sieve has the advanced performance of higher N2 adsorptive capacity, larger water absorbing capacity and the like. On the basis of modified treatment, the invention also provides a preparation method of an NH4 molecular sieve and an ultrastable Y-shaped molecular sieve, which comprises ammonium exchange treatment and hydrothermal ultrastable treatment implemented for a modified NaY molecular sieve after alkali treatment, and the obtained NH4 molecular sieve has lower metallic ion residues; an obtained USY molecular sieve has more abundant secondary holes while keeping high degree of crystallinity, thereby improving the catalytic activity of the USY molecular sieve.

Provided is a method for heating coal seam and extracting coal seam gas. Firstly, a plurality of vertical wells are drilled from the ground to the coal seam, after the drilled well reached to the coal seam, the coal seam is inserted with a screen tube casing (4), the section above the coal seam is inserted with a heat insulation casing (31) and the well is correspondingly fixed. At least one well of the wells is selected to be a heat source injection well (1) and other wells are gas production wells (2), steam with high temperature and high pressure is injected into the heat source injection well (1) to perform fracturing to communicate all the wells in the network. Drainage and pressure reduction are performed to the gas production wells (2) to extract the mixed gas of the coal seam gas and steam. The mixed gas of the coal seam gas and steam is cooled by known cooling method so as to obtain gaseous coal seam gas and liquid distilled water to realize the separation of the mixed gas. According to the change of the coal seam temperature, the heat source injection well (1) and the gas production wells (2) are allocated to control the heated coal seam and extract coal seam gas. The method of he invention can effectively perform the extraction of the coal seam gas, accelerate the coal seam extraction speed, and improve the extraction rate.

The invention relates to a preparation method for aromatic series polybenzimidazole resin film, comprising: (1) under function of polyphosphoric acid/phosphorus pentoxide system, condensation polymerization reaction is carried out to aromatic series amine and aromatic series dicarboxylic acids mixed according to mol ratio of 1:1 in nitrogen atmosphere; (2) after cooling, polymer is poured into water and broken down into powder in a resin pulper and washed over and over again by distilled water and soaked for 48 hours in NaHCO3 solution and washed till pH value shows neutral and drawn and filtered for drying in vacuum; (3) the polymer dried is dissolved in even solution prepared by organic solvent with mass percent of 5 percent, and then is dried at temperature of 130 DEG C for 12 hours, and is soaked in hot water for boiling and striping, and is dried in vacuum at temperature of 100 DEG C for 5 hours and then is obtained. The polybenzimidazole prepared by the invention has the advantages of big molecule weight, stable thermal stability, fine solubility and film forming performance, etc. The preparation has simple technology, low cost, convenient operation and can be finished in common equipments through preparation procedure.

The present invention provides aqueous parenteral formulations containing an antiarrhythmic agent, such as amiodarone, and a sulfoalkyl ether cyclodextrin. The liquid formulations are clear, sterilizable, and chemically and physically stable. The liquid formulations do not require a surfactant and do not precipitate upon dilution with distilled water or other pharmaceutically acceptable liquid carrier. The sulfoalkyl ether cyclodextrin-containing formulation provides significant advantages over other cyclodextrin-containing formulations of amiodarone. The formulation can be prepared in acidic, neutral and slightly basic medium while providing acceptable concentrations of amiodarone suitable for parenteral administration. An SAE-CD-containing formulation of amiodarone can be provided in liquid form or as a reconstitutable powder. Moreover, highly concentrated solutions exceeding 200 mg of amiodarone per mL can be prepared. Solutions can be made either dilutable or non-dilutable with water at room temperature or under conditions typically encountered in the clinic.

The invention provides an expanded flexible well cementing grout and a preparation method thereof. The grout comprises the following components in parts by weight: 100 parts of cement, 6-14 parts of toughening material, 3-80 parts of reinforcing material, 8-120 parts of density modifier, 0.5-2.5 parts of suspension stabilizer, 20-40 parts of high-temperature stabilizer, 35-100 parts of distilled water, 0.5-2 parts of dispersant, 0.5-4 parts of fluid loss agent, 0.3-4 parts of retarder, 0.1-2 parts of foam inhibitor and 0.1-2 parts of defoamer. The invention further provides a preparation method of the expanded flexible well cementing grout. The grout has good sedimentation stability; and the set cement has the characteristics of micro expansion, high strength and low elasticity modulus, and can avoid the phenomena of micro cracks, micro annuluses, even fracture and the like caused by cement sheaths in subsequent operation of gas storage wells, shale gas wells, dense oil-gas horizontal wells and the like, thus realizing good zonal isolation and providing a technical support for long-term, safe and effective operation of oil-gas wells.

The invention relates to a watery zinc-aluminium heavy-duty coating in a compounding squama shape and a preparation method thereof. The watery zinc-aluminium heavy-duty coating belongs to a bi-component coating and is prepared from organic-inorganic modified base stock and pigment according to a certain proportion by weight, wherein the organic-inorganic modified base stock contains silica sol, potassium hydroxide, silicone-acrylate emulsion, a pigment dispersing agent, a film forming addition agent and an antifoaming agent, and the balance is deionized water or distilled water; the pigment comprises squama-shaped zinc powder and squama-shaped aluminium powder; and the weight ratio of the organic-inorganic modified base stock to the pigment is 5: 1-2. The watery zinc-aluminium heavy-duty coating contains no chrome, can be solidified at the normal temperature, has environmental protection and low energy consumption and can be used for preparing thin coatings with high corrosion resistance, and the like.

Disclosed are a preparation method and application of heterogeneous Fenton-like catalyst. The preparation method includes the steps of firstly, dissolving complexing agent and metal salt in distilled water to respectively prepare complexing agent and metal salt solutions; secondly dropwise adding the metal salt solution into the complexing agent solution under the action of a magnetic mixer, and mixing for 20-60 after dropwise addition to obtain metal complex solution; and thirdly, impregnating activated carbon fiber in the metal complex solution for 1-24h, and subjecting taken-out activated carbon fiber to distilled water washing and drying to obtain the heterogeneous Fenton-like catalyst. The preparation method is simple, and conditions are mild. Environment-friendly hydrogen peroxide is used as oxidant, no extra ultraviolet light or even visible light is needed, and the heterogeneous Fenton-like catalyst is capable of efficiently degrading organic pollutants such as dye within a wide pH range of 2-10. The heterogeneous Fenton-like catalyst is well repeatable, and secondary pollution of the homogeneous Fenton reagent caused by iron ions is avoided.

The invention relates to a preparation method of nickel-coated alumina oxide powder, in particular to the preparation method of nickel-coated aluminum oxide powder for thermal spraying in aviation, aerospace and military fields. The invention is characterized in that: a suspension is made from a mixing liquid of nano-aluminum oxide and dispersant, stirred and added with nickel salt solution at the same time, and the obtained mixture liquid is dropped with ammonium water after being fully stirred, added with distilled water, when dark blue mixing solution C of nickel ammonia complex ([Ni (NH3)) 2+and alumina oxide is obtained; the mixing solution C is aged by water, filtered, washed and dried, and a green middle coated product is obtained; the green middle coated product is further reduced and roasted, finally, black nickel-coated aluminum oxide powder is prepared. The nickel-coated aluminum oxide powder prepared through the invention has uniform granularity, with average size less than or equal to 1.0Mum, and can enhance the application performance of nano-alumina and expand the application of nano-aluminum oxide; the product is mainly used for aviation, aerospace and military materials and other high-tech fields. The method of the invention is simple, reproducible and easy to be industrialized.

A machine cleaner tablet comprising from about 10 to about 75% of a limescale remover acid, from about 1 to about 20% of low foaming non-ionic surfactant, from about 0.5 to about 5% of a detergency enzyme and wherein the tablet has a pH measured as a 1% solution in distilled water at 20° C. in the range from about 1 to about 5. The tablet is used for cleaning the interior of automatic dishwashers, food processing machines and the like.

The method of reducing loaded metal catalyst with low temperature plasma includes the steps of: 1) dissolving active metal salt component in deionized water or distilled water to form solution with metal component content of 0.01-20 wt%, filling solution into catalyst carrier, letting stand at room temperature for 8-24 hr and drying at 40-110 deg.c for 2-10 hr; and 2) setting the catalyst between two electrodes of plasma apparatus, introducing inert gas, air or oxygen as plasma discharge gas into discharge tube of pressure of 50-10000 Pa, and applying DC or AC voltage of 100-20000 V across the electrodes to process for 5-200 min. The low temperature plasma contains great amount of electrons, has powerful reducing capacity to reduce metal ion into metal simple substance and has no negative reaction appearing at high temperature. The process is simple, short in reduction time, without need of chemical reductant and environment friendly.

A process for preparing the hydrosol of nano-class anatase-type TiO2 features that reaction between Ti-contained organic substance, distilled water or deionized water, chelating agent and hydrodecomposing inhibitor at 30-120 deg.C for 3-12 hr while stirring and controlling pH=1-5.

The invention discloses a print molding method for 3D object and support that the process includes the following steps: building up computer solid model, taking slicing and delaminating, the printing nozzle spraying UV liquid material and moving according the information set according to the layers, solidifying to form slice sheet; spraying supporting material to fill the blank area, concreting to solid state to be used for the support for the next layer; superposing to form 3D object and support. The support material could be one from distilled water, watercraft liquid, solvent-liquid, and dyestuff type liquid that would form support after concreting. After making the 3D object, heating until melting, the 3D object would be gained. The invention would be fast, reliable, safe and low cost to make a complex 3D object. It is asepsis, either.

The present invention relates to a water soluble chitosan nanoparticle (WSC-NP) for delivering an anticancer agent and a preparing method thereof, more precisely, a water soluble chitosan nanoparticle for delivering an anticancer agent which has function of targeting on a wanted area by introducing a functional group in the location of highly reactive amine group and becomes an excellent gene carrier with the use of water soluble chitosan since the water soluble chitosan itself can combined with DNA having a negative electric charge(−) owing to the very strong positive electric charge(+) of its amine group, and a preparing method thereof. Therefore, a water-soluble chitosan nanoparticle for delivering an anticancer agent of the present invention can effectively envelope paclitaxel by introducing hydrophilic and hydrophobic groups in the position of highly reactive amine group of the water-soluble chitosan. A water soluble chitosan nanopaclitaxel prepared as the above has an excellent re-dispersion force, after freeze-drying, in distilled water and has an outstanding anticancer effect with its accumulation in tumor cells greater than that of the other anticancer agent carriers.

The invention discloses an electric pressure pot cover with a water guide groove, which comprises a pot cover body (1), and is characterized in that a water guide groove (2) is formed on the inner surface of the pot cover body (1), and the water guide groove ( 2) It is used to divert the distilled water condensed on the lid body (1) to the bottom side of the lid body (1) after the lid is opened. The drain hole (3) of the body (1). The electric pressure cooker cover with water guide groove proposed by the present invention, by setting the water guide groove on the inner surface of the pot cover body, distilled water can flow into the bottom of the inner surface of the pot cover after the water guide groove is opened, and be discharged through the drain hole. This prevents the hot distilled water from falling freely and prevents the user from being scalded.

A gravity fed carbon block water filter includes activated carbon particles; a binder material interspersed with the activated carbon particles; and a lead scavenger coupled to at least one of the activated carbon particles and binder material, the lead scavenger being for removing lead from water, where a lead concentration in a final liter of effluent water filtered by the filter is less than about 10 μg/liter after about 151 liters (40 gallons) of source water filtration, the source water having a pH of 8.5 and containing 135-165 parts per billion total lead with 30-60 parts per billion thereof being colloidal lead greater than 0.1 μm in diameter, and where the water has an average flow rate of at least 0.1 liter per minute through the filter with a head pressure of between approximately 0.1 and 1.0 psi.

The invention discloses a fatty group end-amino polyether production method and special catalyzer preparation method, wherein the catalyst is special-purposed frame nickel catalyst, the custom made alloy is dissolved completely by sodium-hydroxide liquor under finite temperature and proportioning conditions, then distilled water is used for scouring to neutrality, then anhydrous alcohol is used for washing and sealing. The process for preparing the end-amino polyether comprises using the said special-purpose catalyst for reaction under finite concentration, temperature and proportioning conditions, thus the end-amino polyester can be obtained.wh

A cleaning method for a combustor comprises positioning a spray portion of a nozzle through an igniter plug boss and spraying an acid solution inside the combustion chamber. The acid solution impinges the inner liner and the outer liner, dissolving contaminant deposits inside the effusion holes. The nozzle can have a second spray portion outside the combustion chamber to provide acid solution to the radially outward surface of the outer liner. After cleaning, distilled water is sprayed through the nozzle to remove the acid solution residue from the combustor. The used acid solution and distilled water can be collected, filtered and pumped through the nozzle to provide a recirculating cleaning/rinsing system.

The invention discloses a polysaccharide-dopamine composite biogel and application of the biogel. A preparation method of the biogel comprises the following steps: dissolving 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and N-hydroxy succinimide sodium in an MES (Methyl Ester Sulfonate) buffer solution with a pH value being 5-6 in an inert gas atmosphere so as to prepare an EDC (ethylcarbodiimide) mixed solution, subsequently adding the EDC mixed solution into a polysaccharide solution for reacting at 20-30 DEG C for 0.5-1 hour, then adding a dopamine solution for further reacting at 20-30 DEG C for 1-4 hours, dialyzing a reactant by taking distilled water as a dialyzate, taking trapped fluid for freezing and drying to obtain the polysaccharide-dopamine composite biogel. The polysaccharide-dopamine composite biogel is simple and effective in modification method and capable of increasing the surface viscidity of the cartilage tissue, reducing loss of therapeutic drugs or implanted cells and facilitating the repairing of the cartilage injury.

The invention relates to a low-temperature soap-making process of natural cooling-making soap, which belongs to a washing article and a making process thereof. The cooling-making soap is made of the following raw materials in proportion by weight at low temperature: 20-28 distilled water, 60-71 base grease, 6-12 sodium hydroxide, essential oil accounting for 0.5-1.5 percent of the total weight ofthe distilled water, the base grease and the sodium hydroxide, and Chinese medicine accounting for 1.5-2.5 percent of the total weight of the distilled water, the base grease and the sodium hydroxide.The making process comprises the following steps: firstly, weighing the raw materials; secondly, adding the sodium hydroxide into the distilled water; thirdly, adding the base grease into a stainlesscontainer, heating by separating from water; fourthly, after reducing the temperature of the sodium hydroxide solution and the base grease solution, slowly pouring the sodium hydroxide solution intothe base grease solution, and completely stirring uniformly; fifthly, adding the essential oil and the powder of the Chinese medicine, and stirring uniformly; sixthly, pouring the liquid mixture intoa mould, demoulding, and standing thus obtaining the soap. The invention solves the problem of poor washing effect of the washing soap produced by the prior art.

The invention provides a method for preparing hard polyurethane foam plastics from soybean oil. The method comprises the steps as follows: (1) carrying out epoxidation including the sub-steps of subjecting soybean oil and epoxidizing agent to reaction to obtain epoxidized soybean oil; (2) carrying out ring-opening reaction including the sub-steps of subjecting epoxidized soybean oil and nucleophilic reagent of reactive hydrogen to the ring-opening reaction of epoxy chemical bond in the presence of a catalyst to obtain mixed hydroxyl fatty acid glyceride; (3) carrying out alcoholysis and esterification including the sub-steps of adding alcohol, heating for alcoholysis to obtain mixed hydroxyl fatty acid monoester, i.e. soybean oil based polyol, and esterifying with organic acid and acid anhydride to generate polyester polyol; and (4) sequentially adding 80-150 weight parts of isocyanate, 0.3-4 weight parts of triethanolamine and 0.5-4 weight parts of foam stabilizer to 100 weight parts of soybean oil based polyol, intensively stirring, adding 0.5-3 weight parts of distilled water, and uniformly foaming while stirring at the high speed.

The invention relates to a method for preparing graphene oxide by chemical peeling, belonging to the field of graphene oxide preparation. The method comprises the following steps: (1) graphite oxide preparation: selecting expanded graphite, strong acid, oxidant and distilled water according to the proportion of (0.1-0.8g):(10-90ml):(0.6-12g):(40-300ml); mixing the expanded graphite with the strong acid evenly, adding oxidant and then carrying out a reaction on the mixture for 0.25-4 hours in a condition of 30-45 DEG C; adding distilled water to react for 0.5-2.5 hours and washing the filter cake to neutral with distilled water; rinsing the filter cake with absolute ethyl alcohol, drying the cake in a condition of 30-45 DEG C to obtain the graphite oxide. (2) graphene oxide preparation: selecting the graphite oxide and organic solvent according to the proportion of (0.02-0.1g):(15-70ml); adding the graphite oxide to the solvent and dispersing with a 40-50kHz ultrasonic sound for 0.5-10 hours; centrifugating at a rate of 3000-5000r/min for 20-90 minutes; taking the suspension solution and drying in a condition of 30-45DEG C to obtain the graphene oxide. The method in the invention is safe in operation and has low costs.

The invention belongs to the technical field of polymer material, and relates to a method, used in a production process, for reducing metal impurities in poly(aryl ether ketone). The method comprises the following steps: 1) purification: fully mixing poly(aryl ether ketone) with hydroxy ethidene diphosphonic acid aqueous solution with mass concentration of 0.1-2% at 40-100 DEG C for 0.5-3 h, wherein time for mixing and stirring is preferably 1-2 h, and filtering; 2) washing: washing the purified poly(aryl ether ketone) with distilled water, until conductivity of the aqueous solution is below 20 muS / cm; and 3) drying: drying the washed poly(aryl ether ketone) at 120-140 DEG C for 4-6 h to obtain poly(aryl ether ketone) with metal impurities removed. The method can not only reduce content of the metal impurities in the poly(aryl ether ketone) and improve product quality; besides the used reagents have excellent chemical stability, small dosage, and no self toxicity or pollution, can be treated with biochemical degradation in a later period of production, and will not harm the environment.