1264 results about "Alkyl sodium sulfates" patented technology

The component of the paper soap include carboxymethyl cellulose sodium, fatty alcohol polyioxymethyl ethyleneethere sodium sulfate, sodium dodecyl benzene sulfonate, lauryl sodium sulfate, cocinin diethanolamide, nonly phenol polyoxyethyleneether, glycerine, quaternary ammonium salt and citric acid. Its preparation includes preparing carboxymethyl cellulose sodium mother liquor, adding the mixed solution of other components to prepare solution through stirring, spraying the prepared solution of PVC plate and drying in a sealed room and moisture extract at 35-40 deg.c to form film.

The invention relates to an expendable pattern casting (EPC) molding shell paint for casting steel, and the EPC molding shell paint comprises surface a layer fireproof paint and a back layer reinforcing paint, wherein the surface layer fireproof paint comprises the following components in parts by weight: 80-90 parts of high-chromium alundum powder, 10-20 parts of calcined kaolinite, 6-8 parts ofcalcium rectorite powder, 1-3 parts of sodium tripolyphosphate, 3-5 parts of polyvinyl formal solution, 0.3-0.5 part of ethoxylated alkyl sodium sulfate, 0.6-1.0 part of polyether type modified polydimethylsiloxane and 60-75 parts of water; and the back layer reinforcing paint comprises the following components in parts by weight: 75-85 parts of coal gangue sand, 15-25 parts of kaolinite, 3-6 parts of feldspar powder, 8-13 parts of calcium rectorite powder, 8-10 parts of sodium tripolyphosphate, 1.5-2.0 parts of wood fiber and 30-45 parts of water. A molding shell manufactured by the surface layer fireproof paint and the back layer reinforcing paint has the characteristics of high strength and refractoriness, good air permeability and the like.

The invention relates to a preparation method of a nano TiO2-modified PVDF (Polyvinylidene Fluoride) ultrafiltration membrane. The preparation method comprises the following steps of: preparing a membrane making liquid from 15-20 percent by mass of PVDF, 1-3 percent of pore-foaming agent, 1-4 percent of nano TiO2, 3-5 percent of surfactant and 70-80 percent of solvent, ultrasonically oscillating the membrane making liquid for 5-10 minutes, leaching and defoaming; scraping with a membrane scraping machine to form a liquid membrane, standing in the air for 20-60 seconds, soaking into a coagulation bath and coagulating the liquid membrane into an ultrafiltration membrane; and after the ultrafiltration membrane falls off, taking the ultrafiltration membrane out, soaking into distilled water and cutting according to required size for later use. A nano TiO2 hydrophilic monomer is arranged on the surface of the PVDF ultrafiltration membrane, sodium dodecyl sulfate serving as a surfactant is used simultaneously, and dispersion is performed by ultrasonically oscillating, so that agglomeration of nano TiO2 is reduced, nano TiO2 is quickly and uniformly distributed into the membrane making liquid, the hydrophilicity of the PVDF ultrafiltration membrane is enhanced effectively, the energy consumption is enhanced greatly, the anti-pollution capacity and pollutant intercepting performance of the membrane are enhanced, and the service life of the membrane is prolonged.

The invention relates to a textile water-based pigment printing binding agent and a preparation method. The textile water-based pigment printing binding agent is prepared in a way that acrylonitrile, ethyl acrylate, butyl acrylate, crylic acid, hydroxyethyl methacrylate, acrylamide, sodium dodecyl sulfate, alcohol dodecyl polyoxyethylene (10) ether, deionized water, ammonium persulfate and sodiumhydrogen sulfite are subjected to emulsion polymerization and then are mixed with pyrolysis closed polyurethane crosslinking agent according to proportion. The product is cured in low temperature condition, has remarkable advantages in the aspects of dry rubbing fastness, wet rubbing fastness, soaping fastness and the like, is simple and easily-controllable in production operation, and is energy-saving and environment-friendly.

The invention relates to a formaldehyde-free environment-friendly vegetable protein modified adhesive, which aims to solve the problem that the prior urea-formaldehyde adhesive, phenolic aldehyde adhesive and melamine aldehyde adhesive release formaldehyde and cause environmental hazard and pollution, etc. The compositions in portion by weight of the modified adhesive are: 30 to 50 portions of natural plant dregs, 5 to 12 portions of basic material, 5 to 10 portions of calcium hydroxide emulsion, 6 to 15 portions of urea, 4 to 10 portions of alkyl sodium sulfate, 2 to 5 portions of 10 to 20 percent of inorganic acid and 90 to 120 portions of deionized water. The invention takes macromolecular proteins in natural plant soybean dregs, peanut dregs, rapeseed dregs, cottonseed dregs, linseed dregs and sunflower seed dregs as raw materials so as to synthesize a new-generation formaldehyde-free environment-friendly vegetable protein modified adhesive through chemical modification. The formaldehyde-free environment-friendly vegetable protein modified adhesive has the characteristics of uniform and stable product, high adhesion strength, hydrolysis resistance and nontoxicity, etc.; moreover, the performance and the price of the modified adhesive are suitable for wood adhesion and for making artificial fiber boards such as plywood, shaving board and fiber board.

The invention discloses recycled aggregate concrete and a preparation method thereof. The recycled aggregate concrete comprises the following raw materials by weight percent: 15 to 20 percent of cement, 5 to 15 percent of water, 15 to 25 percent of third mixed additive, 38 to 63 percent of coarse aggregate, 0.3 to 1 percent of modified wood fiber-containing polyurethane modified epoxy resin flexibilizing emulsion, 0.1 to 0.5 percent of lauryl sodium sulfate, 0.1 to 0.5 percent of sodium gluconate, 0.1 to 0.5 percent of water glass, 0.5 to 1 percent of polyacrylate, and the sum of weight percent of the raw materials is 100 percent; and the coarse aggregate is the waste concrete renewable coarse aggregate or a mixture of waste concrete renewable coarse aggregate and natural coarse aggregate. The renewable aggregate concrete has good impact resistance, earthquake resistance and crack resistance, the pressure resisting strength of the recycled aggregate concrete in 28 days can reach 80 to 100 MPa, and the recycled aggregate concrete is applicable to a load-bearing structure.

The invention discloses a water-based metal cleaner and a preparation method thereof. The water-based metal cleaner is prepared from sodium dodecylbenzene sulfonate, fatty alcohol-polyoxyethylene ether, alkylphenol polyoxyethylene, triethanolamine oleate, triethanolamine, 3-methyl-3-methoxy-1-butanol, polyphosphate, silicate, glycerol, primary sodium alkyl sulfate, isooctyl phosphate, benzotriazole, polyethylene glycol, dimethylaminoethyl methacrylate, 2-hydroyl-3-sulfopropyl starch ether and deionized water; the preparation method of the water-based metal cleaner comprises the following steps: firstly, adding a surfactant and the triethanolamine oleate to the glycerol, heating and stirring, next, adding the triethanolamine, the 3-methyl-3-methoxy-1-butanol, the polyphosphate and the silicate, adding the primary sodium alkyl sulfate, the isooctyl phosphate, the benzotriazole and the polyethylene glycol under the conditions of stirring and preserving heating, and finally adding the rest components under the conditions of stirring and preserving heating, and heating and stirring to obtain the cleaner. The water-based metal cleaner has excellent cleaning performance and relatively high corrosion inhibition period.

The invention refers to a capsule preparation containing tegafur, gimeracil and potassium oxonate. The capsule preparation comprises the following components by weight parts: 20 parts of tegafur, 5-6 parts of gimeracil, 19-20 parts of potassium oxonate, 10-300 parts of lactose, and 0.9-5 parts of sodium dodecyl sulfate. According to the invention, the use level of the surfactant of sodium dodecylsulfate is greatly reduced on the premise of guaranteeing rapid dissolving-out of active components in the preparation, so that the irritation of the capsule preparation to the human gastrointestinaltract is decreased and the medicine compliance of a patient is increased.

The invention provides a plugging agent with a double plugging function and a filling method thereof. The plugging agent comprises a foaming agent, a foam stabilizer, a cross-linking agent, gas and water, wherein the foaming agent is sodium dodecyl sulfate as an anionic surfactant, the foam stabilizer is water-soluble polyacrylamide with relative molecular mass of 11.6*106, and the cross-linking agent is a chromium cross-linking agent and comprises Na2Cr2O7 and Na2SO3. The filling method comprises the following steps: sequentially filling a far-well foaming liquid comprising the foaming agent, the foam stabilizer and the cross-linking agent, transition-area foaming liquid and near-wall foaming liquid; then, filling HPAM (hydrolyzed polyacryamide) over-top replacing liquid and nitrogen; and finally, filling clear water as the over-top replacing liquid for completely replacing the nitrogen into a layer of the earth. The gel foam plugging agent not only has Jamin effect of nitrogen foam, but also has a selective plugging function of polymer gels, improving foam stability by using the gel as an outer phase and increasing the effect and the effective period of a plugging measure.

The invention discloses an anti-flaming antisepsis leather coating which is composed of, by weight, 2-3 parts of hydrous zinc borate, 1-1.5 parts of linoleic acid calcium soap, 0.1-0.2 part of triterpenoid saponin, 0.7-1 part of calcium naphthenate, 1.7-2 parts of polyvinylpyrrolidone, 0.8-1 part of polyacrylamide, 1.6-2 parts of stannous chloride, 0.1-0.13 part of triethanolamine, 190-200 parts of methyl methacrylate, 3-4 parts of lauryl sodium sulfate, 0.1-0.2 part of urotropine, 0.2-0.3 part of ammonium persulfate, 6-7 parts of a 20%-25% formaldehyde solution, 16-20 parts of zinc acetate, 4-7 parts of silver nitrate, 1-2 part of decabromodiphenyl ether and 0.4-1 part of sodium lauryl sulfate. The anti-flaming antisepsis leather coating has a good antibacterial property and excellent moisture permeability and water resistance. Leather coated with the obtained emulsion is good in antibacterial property and excellent in hygiene property.

The invention discloses a nano air purifying catalytic agent and a preparation method thereof. The nano air purifying catalytic agent comprises the following components in percentage by mass: 1%-10% of titanium dioxide, 0.5%-5% of nano platinum, 1%-3% of methylcellulose, 0.5%-1.5% of sodium dodecyl benzene sulfonate, 1%-20% of graphene, 1%-10% of sodium alkyl sulfate, 1%-5% of carboxymethylcellulose, 0.5%-5% of nano negative-ion powder, 0.05%-2% of nano silver and the balance of deionized water. The nano air purifying catalytic agent can continuously purify indoor air for 24 hours in the whole day under the condition of light or no light.

Provided are compositions comprising a hydrophobically-modified acrylic polymer, sodium trideceth sulfate, and one or more particles suspended therein having unexpectedly high stability. Also provided are methods of suspending at least one particle comprising combining at least one particle with a hydrophobically-modified acrylic polymer and sodium trideceth sulfate to produce a composition comprising the hydrophobically-modified acrylic polymer and sodium trideceth sulfate in which the at least one particle is suspended.

The invention discloses a cement base soil-solidified-agent and preparation and application thereof. The soil-solidified-agent is prepared by the following raw materials by weight percent: 10-40% of sodium sulfate, 2-6% of sodium tripolyphosphate, 2-5% of carbamide, 2-8% of polyacrylamide, 1-5% of lauryl sodium sulfate emulsifier, 2-10% of triethanolamine, 10-60% of sodium silicate, 4-12% of sodium hydroxide, 2-15% of sodium carbonate,2-6% of potassium hydroxide and 2-8% of methyl sodium silicate; and the sum of the percentage is 100%. The soil-solidified-agent can be prepared into powder or liquid, can fully activate various physical, chemical and physical chemistry reactions of cement and soil, so as to greatly improve engineering performance of cement soil, improve strength, reduce dry shrinkage and improve durability. The invention can be widely applied to projects such as road foundation, embankment reinforcement, channel seepage prevention, water and soil conservation, side slope protection, pile foundation processing and the like.

The invention relates to a nifedipine sustained release tablet and a preparation method thereof. The nifedipine sustained release tablet is characterized by comprising a tablet core and film coating liquid, wherein the tablet core comprises the following components in percentage by mass: 10 to 12 percent of nifedipine (Nif), 6.5 to 7.5 percent of hydroxypropyl methyl cellulose K4M, 45 to 47 percent of lactose, 34 to 35 percent of microcrystalline cellulose, 0.48 to 0.55 percent of lauryl sodium sulfate, a proper amount of 95 percent ethanol and a proper amount of magnesium stearate; and the film coating liquid comprises the following component in percentage by mass: 5.85 to 6.55 percent of Opadry II and 92.86 to 93.82 percent of distilled water. The preparation method comprises the following step of: mixing the nifedipine and polymer by utilizing the imported polymer and dispersion technology to form a hydrophilic matrix tablet so as to fulfill the aim of sustained release. Compared with an ordinary tablet, the sustained release tablet can continuously act for 12 hours relaxatively, is released in a sustained way and has less and slighter adverse reaction.

The invention relates to a high-boiling point monocrystalline silicon wafer surface texturing additive and a using method thereof and belongs to the technical field of production of solar cells. The additive is prepared from the following raw materials in percentage by weight: 0.01 to 3 percent of sodium alginate, 0.01 to 3 percent of trisodium phosphate, 0.001 to 1 percent of lauryl sodium sulfate, 0.1 to 2 percent of vitamin, 0.1 to 5 percent of propylene carbonate and the balance of deionized water; when the additive is used, a sodium oxide solution is needed to be added into the additive so as to obtain a texturing solution; the volume percentage ratio of the additive to the sodium oxide solution is (0.1-5):100; the temperature of the texturing solution is 70 to 90 DEG C; and the texturing time of the monocrystalline silicon is 600 to 1,500s. The reaction speed is controlled by using high viscosity of the sodium alginate, and the concentration of sodium hydroxide is increased simultaneously, so that a pyramid texture which is uniform in size is obtained; and the sodium alginate has the chelation function on metal and the function of cleaning the silicon wafer, and is low in cost.

The invention relates to the porous ceramics material field, and concretely relates to a method for manufacturing high porosity and high strength yttrium-silicon-oxygen porous ceramics material through a foaming injection coagution process. According to the method, yttrium oxide and silicon oxide mixed power can be taken as a raw material, water is taken as a disperse medium, polyethyleneimine or ammonium citrate is selected as a dispersant, acrylamide or N-methylolacrylamide is taken as a monomer, a cross-linking agent N,N'-methylene bisacrylamide is added, a foaming agent sodium dodecyl sulfate, a peeling inhibitor polyoxyethylene, a catalyst N, N, N',N'-tetramethyl ethylenediamine and an initiator ammonium persulfate are added after stirring, and then injection mold solidification is carried out, drying is carried out for 24-48 hours at room temperature after demoulding, and then drying is carried out for 24-36 hours under the temperature of 60-90 DEG C, high temperature reaction sintering is carried out for 1.5-2.5 hours under the temperature of 1500-1550 DEG C finally, and the gamma-Y2Si2O7 porous ceramics can be finally manufactured. The manufactured gamma-Y2Si2O7 porous ceramics material having a multi-layer pore structure has controllable porosity with high porosity (75-85%) and high strength (3-8MPa).

The invention provides a sound absorbing decorative gypsum board and a production method thereof, and relates to a decorative panel. The sound absorbing decorative gypsum board comprises an aluminiumfoil (1), a paper-faced gypsum board (2), and an embossing relief (3). The paper-faced gypsum board (2) is prepared by the following raw materials according to the proportioning rate: 60 parts of desulfurization gypsum, 4 parts of modified starch, 1 part of foaming agent, namely lauryl sodium sulfate, 1 part of glass fiber and 34 parts of water. The product is manufactured by the following steps:rotary drum embossing, film adhering of coating and drying. Compared with the existing sound absorbing board with the material quality, such as sound absorbing fiber or mineral wool and the like, thesound absorbing decorative gypsum board has the advantages of simple manufacturing process, high strength, dampproof performance, long service life and good effect of noise reduction and sound absorption.

The invention discloses a formula of flame-retardant polyvinyl chloride (PVC) plastics. The formula is characterized by comprising PVC and supplementary additives, wherein the supplementary additives include a flame retardant, a mildew preventive, an antistatic agent, a heat-resisting agent, a crosslink agent and a coupling agent, the flame retardant is triphenyl phosphate and ammonium polyphosphate, the mildew preventive is 8-hydroxyquinoline copper, the antistatic agent is sodium alkyl sulfate, the heat-resistant agent is 2-ethylhexyl thioglycolate, the crosslink agent is 2,5-dimethyl-2,5 bis(tert-butyl peroxy hexane and the coupling agent is aminopropyltriethoxysilane. The flame retardant is used for improving the flame-retardant property of the PVC plastics; by adding multiple assistants in the flame-retardant PVC plastics, the heat resistance and the antistatic property of the flame-retardant PVC plastics can be improved, the stability of the flame-retardant PVC plastics also can be improved, and the production cost can be reduced by accelerating the reaction speed and reducing the consumption of raw materials.

The invention relates to a CuO/TiO2 nanotube array and a preparation method and an application method thereof. The preparation method comprises the following steps of: depositing elementary Cu nanoparticles on a TiO2 nanotube array in a standard three-electrode system by using aqueous solution containing 0.005 to 2mol/L CuSO4.5H2O as plating solution; putting the CuO/TiO2 nanotube array into mixed solution of 0.25 to 0.5mol/L NaOH, 5 to 15mmol/L K2S2O8 and 10 to 25mmol/L sodium lauryl sulfate, and oxidizing; and calcining the modified TiO2 nanotube array under the aerobic condition. The CuO/TiO2 nanomaterial with a novel structure has high specific surface area, a high electron transport rate, and a wide application prospect in the aspects of solar cells, photocatalysts, sensors and the like.

The invention discloses a polymer system in controllable association strength. The polymer system comprises a subject cyclodextrin polymer and an object surfactant; the subject cyclodextrin polymer is selected from linear cyclodextrin polymer and modified Nano-SiO2 star-shaped macromolecule cyclodextrin polymer; the object surfactant is selected from adamantine-sodium octadecyl sulfate, adamantine-lauryl sodium sulfate, adamantine-cetyl sodium sulfate, benzyl-sodium octadecyl sulfate, benzyl-lauryl sodium sulfate and benzyl-cetyl sodium sulfate. In an application, the cyclodextrin polymer is prepared into an aqueous solution in the concentration of 0.1-0.5g/ml and then is mixed with the surfactant, the cyclodextrin advantage is utilized to wrap adamantine or benzene ring while the alkyl hydrophobic chain is exposed on the exterior of the cyclodextrin hydrophobic chamber, so that the polymer system in controllable association strength can be realized, the system viscosity is changed and the purpose of dynamically regulating the system viscosity can be achieved.

The invention relates to valsartan capsules and a preparation method thereof. The valsartan capsules comprise the following components in parts by weight: valsartan 50-200 parts, microcrystalline cellulose 30-160 parts, crosslinked povidone 1-10 parts, sodium dodecyl sulfate 0.8-4 parts, povidone K30 1-9 parts, and magnesium stearate 1-3 parts. The valsartan capsules provided by the invention canbe used for treating mild and moderate primary hypertension. The valsartan capsules have the advantages of reasonable formula, feasible process, stable and reliable quality, and good stability, dissolution and bioavailability. The valsartan capsules are prepared by using a wet granulation process, the addition method of solubilizer sodium dodecyl sulfate is proper, the concentration of the bonding agent is proper, and the granules have angle of repose smaller than 40 degrees, belong to powders with good fluidity and can meet the need of capsule filling. The valsartan capsules have short production process and low production costs, and are easy for industrial production.

Production of particle lauryl sodium sulfate is carried out by delivering liquid or cream lauryl sodium sulfate feed liquid into atomizer in bottom of atomizing granulating fluidized bed by pressure pump, heating air by heat exchanger, entering into bottom of fluidized bed, contacting with material by distributing board on fluidized bed, fluidizing material, continuously atomizing feed liquid by atomizing nozzle of atomizer, coating onto fluidized particle surface, particle growing, contacting with hot air, drying, fluidizing, coating, drying, particle growing to required particle size, lowering temperature of discharging section, discharging from fluidized bed, screening, and packing. Its advantages include low cost, reasonable process, no environmental pollution, and good fluidity and dissolubility.

This invention is a pulping digestion auxiliary agent of paper making. It is prepared by the feed of fatty alcohol-polyexythelene ether, alkyl sodium sulfate, the putylnaphthalene monosulfonic acid, the sodium pyrophosphate, carboxyme-thylcellulose sodium, sodium sulfate, sulfuric acid and the deionized water. It can be gauging canned after the uniform mixing. This invention is strong acid, strong alkali and high temperature fastness, and it has good dispersion and filtration in water. It can reduce the amount of alkali usage, shorten the time of distillation. The production of this invention is sanitary.

The invention relates to a preparation method of nano silicon dioxide, which comprises the following steps: carrying out hydrolytic condensation on tetraethylorthosilicate by using alanine as a structure guide agent to obtain a silicon dioxide crystal seed suspension; preparing a low-concentration crystal seed suspension; adding sodium lauryl sulfate and sodium silicate; and slowly and dropwisely adding a sulfuric acid solution to regulate the pH value of the system so that the silicon dioxide generated by the hydrolytic condensation of silicate grows on the external surface of the silicon dioxide crystal seed, thereby obtaining the silicon dioxide spheres. Nano silicon dioxide with different specific areas and pore structures can be prepared by regulating the surfactant concentration, aging temperature and roasting temperature; and the specific area is 193-305 m<3>/g, the pore volume is 1.25-1.68 cm<3>/g, and the pore size is 17-34nm. Compared with the existing preparation method, the nano silicon dioxide prepared by the method provided by the invention has the advantages of more uniform particle size and more centralized pore size distribution, thereby having favorable application prospects.

The dispersive tamosxifen citrate tablet is prepared through mixing tamosxifen citrate powder of 25 micron below size, microcrystal cellulose, lactose, PVP, sodium dodecyl sulfate and partial sodium carboxymethyl cellulose; pelletizing the mixture into disintegrated pellets of 0.5 mm below size; adding magnesium stearate and the rest sodium carboxymethyl cellulose; and tabletting into the dispersive tablet. The dispersive tamosxifen citrate tablet can disintegrate fast within 2 min and has fast medicine digesting speed and high bioavailability.