94results about How to "No gel phenomenon" patented technology

Hyper-concentrated liquid detergent comprises, in percentage by weight, 8-30% of anionic surfactant, 40-60% of nonionic surfactant, 5-15% of cosolvent, 0-10% of auxiliary, 0.005-1% of deflocculant, 0-0.5% of fluorescent brightener, 0-2% of detergent enzymes, 0-0.1% of preservative, 0.1-1% of essence, and the balance of water. The hyper-concentrated liquid detergent has the advantages of high solid content and high deterging effect.

The invention provides a modified urea-formaldehyde resin adhesive low in formaldehyde residue and a production method thereof. The modified urea-formaldehyde resin adhesive is characterized by being prepared from the following raw materials in parts by weight: 100 parts of modified urea-formaldehyde resin, 20-25 parts of reinforcing agent and 0.1-0.2 part of defoamer, wherein the reinforcing agent is any one or a composition of several of white carbon black, titanium dioxide, calcium carbonate and kaolin having the particle size greater than 300 meshes; the defoamer is polydimethylsiloxane or tributyl phosphate. The formaldehyde residue of the modified urea-formaldehyde resin adhesive provided by the invention is less than 0.1 mg/L; the modified urea-formaldehyde resin adhesive is used as an adhesive for an artificial board; as the modified urea-formaldehyde resin adhesive is low in release amount of formaldehyde, the health of customers is protected.

The present invention is process of preparing water soluble epoxy resin curing agent. The preparation process includes the following steps: 1. ring-opening reaction of polyethylene glycol and bisphenol A type epoxy resin under the action of catalyst to produce modified epoxy resin with epoxy groups in two ends; 2. dropping the modified epoxy resin into polyethylene polyamine to produce end amino-epoxy addition compound; 3. dropping compound 501 into the addition compound to produce end capping product; and 4. dropping organic acid into the end capping product to form salt and adding certain amount of water to produce the water soluble epoxy resin curing agent. The synthesized curing agent has high water solubility, capacity of well controlling reaction with polybasic amine and high flexibility.

The invention discloses a special compatilizer for improving hydrolysis heat stability of a PC/ABS (polycarbonate/acrylonitrile-butadiene-styrene) alloy and an alloy. The compatilizer is a terpolymer formed by copolymerizing aromatic vinyl monomer, acrylonitrile monomer and glycidyl methacrylate. The PC/ABS alloy with high hydrolysis heat stability comprises the following components in percentage by weight: 50-85% of PC, 10-45% of ABS, 0.5-5% of compatilizer, 0.1-1% of antioxidant and 0.1-0.5% of lubricant. Compared with the prior art, the special compatilizer for the PC/ABS alloy can be blended with other raw materials and subjected to extrusion and granulation in the preparation process to obtain the PC/ABS alloy with excellent hydrolysis heat stability on the premise of maintaining excellent mechanical properties in a simple, effective, convenient and cheap way.

The invention discloses a preparation method of a lithium ion battery high-nickel positive electrode material slurry, and relates to lithium ion batteries. The preparation method comprises the steps: 1) adding an adhesive in a solvent, stirring, after dissolving, adding acetone, stirring, then adding an additive after the solution is swelled, stirring, carrying out vacuum deaeration, and thus obtaining a mixed adhesive solution with the additive and the adhesive; 2) adding a positive electrode active material and a conductive agent to the mixed adhesive solution obtained in the step 1), stirring for 0.5-1 h at the speed of 600-900 r/min, after preliminary pre-mixing of the slurry, stirring for 6-7 h at the stirring speed of 2000-3000 r/min to obtain a battery slurry, filtering, and thus obtaining the lithium ion battery high-nickel positive electrode material slurry. The prepared high-nickel positive electrode material slurry has no gel-forming phenomenon and has good slurry liquidity; and the material processability is extremely superior during production of a lithium ion battery positive electrode piece, and the battery has good electrochemical performance after the slurry is made into the battery.

The invention discloses a washing composition as well as a preparation method and application of the washing composition. The washing composition is prepared by taking water, alkyl polyglucoside, propylene glycol, alkyl betaine, sodium lauryl sulfate, flos lonicerae extract, chrysanthemum extract, radix sophorae flavescentis extract, mint extract, table vinegar (edible acetic acid), table salt, edible essence and a thickening agent as raw materials, and has the functions and characteristics of sterilization and disinfection, oil removal and stain removal, itching stopping and skin protection, odor removal and deodorization, low foam, and capability of being cleaned by washing; meanwhile, alcohol, an alkali, a preservative and other disinfection components are not added, so that a functional skin-protection daily chemical washing product, which can be used for naturally killing viruses and sterilizing, removing oil and dirt, stopping itching and dandruff, resisting allergy and protection skins, and has a medicine effect, is obtained.

The invention provides a solvent method for extracting and making curdlan, relating to the purification and extraction as well as production technique of curdlan products. The technical proposal is as follows: (1) an organic solvent such as alcohol and isopropanol is taken as a dehydrating agent to dehydrate the curdlan aqueous alkali, the gel phenomenon does not exist in the production process, thereby being easy to remove water, salinity and pigment; (2) after the curdlan and the organic solvent are mixed, the solid and liquid are separated by adopting the layered overflow way; (3) the organic solvent is applied for a plurality of times to extract the curdlan with a plurality of times of dehydration. The method adopts the organic solvent method to purify and extract as well as produce the curdlan, and has an extracting yield more than 90 percent; the product has high purity quotient and good quality; the production process can realize the serialization and the automation.

The invention relates to an anti-oxidation paint of fireproof carbon-containing materials which comprises (by weight ratio) filling material 48-72%, yellow dextrin 2-4%, silicon micronized quartz powder 4-10% and balancing water. The invention realizes good storage stability, thus no gelatin phenomenon will happen after long period of storage.

The invention relates to the technical field of a resin and a preparation method thereof, particularly a photocuring resin containing polyethoxy bisthiophenyl fluorene structure and a preparation method thereof. The preparation method comprises the following steps: adding 9.9-(4-thiophenyl-hydroxypolyethoxy)bis fluorene and (methyl)acrylic acid into an organic solvent, and carrying out esterification reaction by using an organic acid as a catalyst in the presence of a polymerization inhibitor and a reducer; and after the reaction finishes, carrying out salt washing, neutralization, water washing, drying and reduced pressure distillation to remove the solvent, thereby obtaining the 9.9-(4-thiophenyl-(methyl)acryloyloxypolyethoxy)bis fluorene. The polyethoxy acrylate resin containing bisthiophenyl fluorene structure is a colorless or light yellow transparent photocuring resin, has favorable heat resistance and transparency, and has different refractive index gradients.

The invention discloses a preparation method of starch-grafted dicyandiamide formaldehyde polycondensate flocculants. The preparation method includes the steps: (1) adding formaldehyde and ammonium chloride in a reaction kettle to react for 0.5-1.0h at the temperature of 40-80 DEG C, then adding dicyandiamide to react for 1.0-2.0h, and adding acrylamide and the formaldehyde to react for 0.5-2.0h so that a cationic polymer including C=C double bonds is obtained; and (2) taking, by weight, 5-10 parts of starch, 5-15 parts of the cationic polymer including the C=C double bonds prepared in the step (1), 0.01-1.0 part of initiators and 75-90 parts of deionized water to react for 1-4h in the presence of nitrogen gas at the temperature of 70-85 DEG C. The flocculants prepared by the preparation method are good in decoloring flocculation effect, less in consumption and low in cost and is suitable for flocculating decoloration of industrial sewage such as printing and dyeing and papermaking and urban sewage.

The invention provides a process and devices for chemical modification of cellulose and for continuous low temperature solution spinning. The process for the chemical modification of the cellulose and for the continuous low temperature solution spinning comprises: after vacuum drying the cellulose, uniformly mixing the dried cellulose with an ionic liquid and modified small molecules in a certain proportion to obtain a mixture, extruding the obtained mixture by a double-screw extruder, and washing the extruded product successively by water and ethanol solvent, drying, crushing to obtain a modified cellulose powder; adding the modified cellulose powder and a solvent in a certain proportion to a mixing kettle, after stirring and mixing uniformly at the room temperature, carrying out extrusion, deaeration, and filtration by using the double-screw extruder, then putting into a spinning assembly, spaying out of a spinneret of the spinning assembly to obtain fibers, putting the obtained fibers successively into a first coagulation bath and a second coagulation bath to rapidly solidify and stretch into solids, after water washing in a water tank, and winding into modified cellulose fibers. The process and the devices can substantially enhance the spinning efficiency, and improve the cellulose fiber performance.

The invention relates to a preparation method of a fluorosilicon modified polyether polymer. The method includes: (1) subjecting polyether polyol to dehydration and degassing under a 90-130DEG C vacuum condition for 1-4h, then performing cooling to 50-80DEG C, adding diisocyanate and a catalyst into polyether polyol; introducing inert gas, stirring the substances evenly, and carrying out reactionat 50-90DEG C for 1-6h, thus obtaining an isocyanate group-terminated polyether prepolymer; and (2) mixing the isocyanate group-terminated polyether prepolymer with a fluorine-containing secondary amino silane coupling agent, and carrying out reaction at 30-90DEG C under inert gas protection for 1-6h till no existence of isocyanato in the system through titration, and ending the reaction, thus obtaining the fluorosilicon modified polyether polymer. The invention also relates to the fluorosilicon modified polyether polymer and the fluorine-containing secondary amino silane coupling agent. The process of termination and modification on the isocyanate group polyether prepolymer with the secondary amino silane coupling agent is easily controllable, no gelation phenomenon occurs, and the product has good preparation reproducibility.

The invention discloses a low foam lubricating liquid for a food beverage chain conveying belt, wherein 0.1-5% by weight of water-soluble emulsified silicone oil, 0.1-5% by weight of alkyl glucoside, 0.1-2% by weight of an anti-foaming lubricant, 0-0.5% by weight of an anti-rust agent, 0-1% by weight of a scale inhibitor, 0.2-1.0% by weight of a preservative, and the balance of water are mixed, and a pH value adjusting agent is added to adjust the pH value to 6.0-7.0 so as to obtain the low foam lubricating liquid. The low foam lubricating liquid has characteristics of good lubricity, good cleaning effect, good water solubility, low foam, no toxicity, no corrosion, good environmental compatibility, easy production, and convenient use.

The invention relates to a room -temperature vulcanized fluorosilicone rubber and a preparation method thereof. The room temperature vulcanized fluorosilicone rubber is prepared from, by weight, 100 parts of a base rubber, 5-10 parts of a cross-linking agent, 1-10 parts of a base material tackifier, 0.05-1 part of a catalyst and 30-100 parts of a colloid reinforcing agent; the base rubber is alkoxy-terminated fluorine-containing polysiloxane; and the cross-linking agent is fluoroalkylalkoxysilane. Compared with traditional dealcoholized RTV silicone rubbers, the room temperature vulcanized fluorosilicone rubber prepared in the invention has the advantages of greatly improved oil resistance, greatly improved antifouling property, greatly improved bonding property, greatly improved storage property and good processability.

The invention discloses a water-borne chromium-free zinc-aluminum anticorrosive paint with phosphomolybdic acid hydrate as a passivating agent. The water-borne chromium-free zinc-aluminum anticorrosive paint with the phosphomolybdic acid hydrate as the passivating agent includes the following components, by mass, 250-310 parts of zinc powder, 10-30 parts of aluminum powder, 3-10 parts of the phosphomolybdic acid hydrate, 110-150 parts of polyethylene glycol, 70-140 parts of a silane coupling agent, 3-8 parts of 2-ethoxyethyl acetate, 1-18 parts of a surfactant, 1-6 parts of a defoaming agent,10-60 parts of tetraisopropyl titanate, 10-18 parts of boric acid and 380-480 parts of deionized water. The polyethylene glycol and the silane coupling agent being 35-50% of the total amount of formula, the 2-ethoxyethyl acetate, the surfactant and the defoaming agent are stirred to be made into an A component; the deionized water, the phosphomolybdic acid hydrate and the silane coupling agent inthe weight ratio and being 50-65% of the total amount of the formula, the tetraisopropyl titanate and the boric acid are stirred to be made into a B component; before use, the A component and the B component are mixed and stirred uniformly according to the weight ratio of 1:1-1.4, and the finished paint is prepared. The thermal stability of the prepared product of the water-borne chromium-free zinc-aluminum anticorrosive paint with the phosphomolybdic acid hydrate as the passivating agent is improved, and a coating after coating conforms to the comprehensive performance requirements of a thincoating, high adhesive strength, good anticorrosive performance and the like required by an automobile fastener.

The invention relates to a preparation method of a double-mercapto-terminal polymer. The preparation method comprises the following steps: reacting a mercapto protection reagent with halomercaptan in a polar solvent according to a molar ratio of 1:1 at -5-5DEG C for 24h, extracting with a weakly-polar solvent, taking the obtained supernatant, evaporating in a rotary evaporator to remove the solvents, and carrying out column chromatography separation to obtain an initiator intermediate, wherein a catalyst used in the above reaction is imidazole, pyrimidine or pyridine; reacting the initiator intermediate with metallic lithium in a non-polar solvent at 30-70DEG C to obtain an initiator, wherein the molar ratio of the initiator intermediate to the metallic lithium is 1:6.7; sequentially adding a solvent, the initiator, a monomer and a structure adjustment agent to a reaction kettle, and reacting at 0-60DEG C to obtain an active polymer; adding a terminating reagent to the polymer, reacting, and adding methanol to terminate; and acidifying the terminated polymer by an inorganic acid to obtain the double-mercapto-terminal polymer. The obtained polymer has the advantages of narrow molecular weight distribution, controllable molecular weight, adjustable chain microstructure, and high functionalization efficiency.

The invention discloses a cationic polymerization method for vinyl monomer. In the method, a reaction medium, the vinyl monomer, an initiator, lewis acid and an additive are used, wherein the reaction medium is a mixed reaction medium comprising an organic solvent and water or completely water; the organic solvent is at least one selected from alkane, naphthenic hydrocarbon and halogenated hydrocarbon; the lewis acid is one or a mixture of substances which accord with a general formula of MXn or YRn-mXm; the additive is an oxygen atom and nitrogen atom-containing organic compound; the molar ratio of the lewis acid to the additive to the monomer is 1.0*10<-3> to 3.2*10<-2>:1.0*10<-3> to 3.0*10<-1>:1; and the materials are reacted at the temperature of between -100 and 50 DE C for 0.5 minute to 2 hours to form a polymerization product, namely polymer with molecular weight of 10<5>. The method can simplifies the process flow, saves the production cost, and has great significance and considerable market application value.

The invention discloses a muscle therapy mineral bath salt. The muscle therapy mineral bath salt is prepared from the following components in parts by weight according to a conventional method: 800 parts of sea salt, 20 parts of C8-10 alkyl glucoside, 10 parts of sandalwood, 5 parts of clove, 15 parts of wrinkled giant hyssop, 2 parts of eucalyptus essential oil and 3 parts of rosemary essential oil. The muscle therapy mineral bath salt disclosed by the invention can effectively relieve muscle pain as well as whiten, exfoliate and moisturize the skin. The muscle therapy mineral bath salt is rich in pure natural traditional Chinese medicine raw materials, and can enable body skin to enjoy bath salt essential nourishing every day and take good care of every inch of the skin. The muscle therapy mineral bath salt is particularly suitable for people with neck and shoulder pain or various muscle pains.

The invention discloses a waterless nano laundry detergent and a manufacturing technique thereof. The waterless nano laundry detergent comprises the following components in parts by weight: 50-65 parts of fatty acid methyl ester polyethenoxy ether, 10-20 parts of alkyl synthol alkoxy compound, 7-9 parts of coconut oil acetal amide, 5-7 parts of sodium lauryl sulfate, 7-9 parts of palm-kernel oil acetal amide and 5-7 parts of propanediol. The manufacturing technique comprises the following steps: adding the sodium lauryl sulfate into the propanediol, stirring uniformly, and heating to 75 DEG C; adding the fatty acid methyl ester polyethenoxy ether, stirring uniformly, and cooling to room temperature; adding the coconut oil acetal amide and palm-kernel oil acetal amide, and stirring uniformly; and detecting to obtain the acceptable product, and packaging. The waterless nano laundry detergent uses plant-derived raw materials, and does not need water as the basic raw material; the active matter content can reach 95%; and the waterless nano laundry detergent is green and environment-friendly, can perform deep cleaning, is easy for rinsing without residues, can be naturally biodegraded, does not pollute the environment, saves abundant transportation resources, and reduces the waste of packaging.

The invention discloses a body-clearing and toxin-removing mineral bath salt. The body-clearing and toxin-removing mineral bath salt is prepared from the following components in parts by weight according to a conventional method: 800 parts of sea salt, 20 parts of C8-10 alkyl glucoside, 10 parts of cassia seed, 5 parts of senna leaf, 15 parts of mulberry leaf and 10 parts of liquorice root. The body-clearing and toxin-removing mineral bath salt disclosed by the invention can promote diuresis, remove toxins as well as whiten, exfoliate and moisturize the skin. The body-clearing and toxin-removing mineral bath salt is rich in pure natural traditional Chinese medicine raw materials, and can enable body skin to enjoy bath salt essential nourishing every day and take good care of every inch of the skin. The body-clearing and toxin-removing mineral bath salt is particularly suitable for people who are prone to growing acnes and blackheads on the backs.