1622results about How to "Good modification effect" patented technology

The invention discloses a method for constructing a functionalized surface and interface by a polydopamine coating layer. The method comprises the following steps: (1) dipping a to-be-modified base material into a dopamine aqueous solution, and automatically forming the polydopamine coating layer on the material surface; (2) preparing an active ester group-containing functionalized polymer; and (3) carrying out an amidation reaction of the active ester group-containing functionalized polymer with the polydopamine coating layer, and carrying out bonding fixation of the functionalized polymer on the material surface, so as to achieve functional modification of the material surface. The method takes the dopamine crosslinking layer having superstrong adhesion performance as a transition layer, is almost suitable for surface modification of any base material, also can overcome a problem that the artificially synthesized functionalized polymer is limited by the dopamine content, and constructs a biomimetic surface having stronger stability.

The invention discloses a method for preparing a modified calcium sulfate whisker by using desulfurization gypsum, comprising the following steps of sieving, pulping, performing hydro-thermal reaction and whisker surface modification, dewatering and drying, wherein the reaction temperature ranges from 107 DEG C to 180 DEG C, the concentration of desulfurization gypsum and water is 5-33wt% and the drying temperature ranges from 100 DEG C to 300 DEG C, and a modifier which is 0.05-5% of the weight of desulfurization gypsum in the calcium sulfate whisker suspension formed in hydro-thermal reaction. The invention solves the problem that CaSO4.0.5H2O whisker is easy to hydrate in the drying process tocause fracture of the whisker and enhances the compatibility of the calcium sulfate whisker and the high polymer materials. The prepared modified calcium sulfate whisker has a diameter of 0.5-6 micrometers, a length of 30-300 micrometers and a diameter ratio of 15-115 and the contact angle of water on the surface of the modified calcium sulfate whisker ranges from 12 to 140 degrees. The invention has the advantages of good modified effect, simple process, low production cost, the use of the non-toxic modifier and environmental-friendly preparation process.

The invention relates to ionic liquid modified natural rubber vulcanized rubber containing graphene oxide. Graphene oxide is modified by use of ionic liquid through a solid grinding method, the modified graphene oxide and natural rubber are mechanically mixed in an open mill or internal mixer, and the formulas such as zinc oxide, stearic acid, an anti-aging agent, an accelerant, a vulcanizing agent, carbon black and the like are added at the same time to obtain natural rubber compound containing ionic liquid modified graphene oxide; and the ionic liquid modified graphene oxide/natural rubber vulcanized rubber provided by the invention can be obtained through vulcanization processing. According to the invention, modified graphene oxide is prepared by use of ionic liquid through the solid grinding method. Under the synergistic effect of the ionic liquid modified graphene oxide and carbon black, the heat conduction coefficient and the mechanical performance of the vulcanized rubber can be improved at the same time. The invention provides a preparation method of novel modified graphene oxide/natural rubber vulcanized rubber with simple technology and excellent performance.

The inveniton provides a hydrophilic modification method for a polytetrafluoroethylene membrane. The method comprises the following steps: step 1, subjecting the polytetrafluoroethylene membrane to plasma treatment under a nitrogen atmosphere, and allowing the surface of the polytetrafluoroethylene membrane to generate relatively-stable free radicals and active sites; step 2, placing the polytetrafluoroethylene membrane into an acylic acid solution and carrying out static impregnation for a period of time, then taking the polytetrafluoroethylene membrane out of the solution and then placing the polytetrafluoroethylene membrane between two glase plates, and carrying out thermochemical polymerization in a vacuum drying oven so as to obtain the polytetrafluoroethylene membrane with the surface grafted with polyacrylic acid; and step 3, subjecting the polytetrafluoroethylene membrane to static impregnation in a titanium dioxide sol for a period of time, and allowing titanium dioxide to be assembled onto the surface of the polytetrafluoroethylene membrane through the coordination effect of metal titanium-ion Ti4+ and a carboxyl group on the polyacrylic acid so as to obtain a hydrophilic modified polytetrafluoroethylene membrane. The hydrophilic modified polytetrafluoroethylene membrane prepared by using the method in the invention retains excellent properties of a conventional polytetrafluoroethylene membrane and greatly improves filter performance, hydrophilic property, pollution resistant property and photocatalytic property of the polytetrafluoroethylene membrane.

The invention discloses a cellulose composite microsphere, a preparation method thereof and application. The particle size of the cellulose composite microsphere is 1mum-1200mum, the specific surface area of the cellulose composite microsphere is 100m<2>/g-500m<2>/g, and the aperture of the cellulose composite microsphere is 200nm-900nm. The preparation method comprises the following steps of: preparing a mixture solution of cellulose and a composite material by using the cellulose as a matrix, a polymer material as composite material and a water solution of alkali/urea or alkali/thiourea as a solvent, and obtaining the cellulose composite microsphere through sol-gel phase transition and cross-linking agent cross linkage. The advantages of cellulose microsphere are reserved by the cellulose composite microsphere, and due to the adding of the composite material, new functional groups are simultaneously added for the surface of the microsphere and further decoration and modification are facilitated. An organic solvent used in the preparation method disclosed by the invention can be reused, the whole preparation technology is simple, low in time consuming, undemanding for equipment and convenient for industrial production, and the prepared cellulose composite microsphere has a good flow property and mechanical property and a wide application.

The invention provides an enzymolysis lignin epoxy resin and a preparation method thereof. The raw materials include: an enzymolysis lignin-dianhydride prepolymer, a glycidol ether, a catalyst, a curing agent and a filler. The preparation method comprises the following steps that: under the action of the catalyst, an etherification of a hydroxyl group contained in the enzymolysis lignin or a derivative of the enzymolysis lignin and dianhydride is carried to synthesize a prepolymer of enzymolysis lignin-dianhydride; then the prepolymer reacts with the glycidol ether and undergoes etherification and ring closing reaction to obtain an enzymolysis lignin--polyester type epoxy resin. The enzymolysis lignin adopted by the method is natural macromolecular material extracted from the residues which is produced in the preparation of alcohol through the fermentation of wood chips, bamboo and stalk, thereby not only effectively utilizing biological resources, but also replacing petrochemical raw materials. The enzymolysis lignin epoxy resin which can be used as a modifier for engineering materials, adhesives, paints and macromolecular materials has a broad application prospect.

The invention discloses a method of atmospheric dielectric barrier discharge plasma to carry out polymer microporous membrane hydrophilic modification. The method comprises the following steps: (1) the polymer microporous membrane is cleaned clearly, dried and then arranged into the solution of an organic monomer for dipping; after the surface of the microporous membrane absorbs the organic monomer, the microporous membrane is taken out and aired; (2) the polymer microporous membrane treated by the step (1) is arranged between the two discharge electrodes of the dielectric barrier discharge to carry out atmospheric dielectric barrier discharge plasma treatment; (3) the polymer microporous membrane treated by step (2) is cleaned and then dried. The method has the characteristics of simple technique, convenient operation, quick processing speed, good and durable processing effect, low cost, being not easy to cause environment pollution, energy saving, and the like.

The invention discloses an energy-saving insulated flame-retardant water-proof corrosion-proof functional coating and a preparation method thereof. The functional coating is prepared from the following raw materials: an aqueous polyurethane dispersion, a flame retardant, a flame-retardant antismoke agent, a hollow glass bead, a wetting dispersant, an anti-settling agent, a thickening agent, water, a leveling agent and a de-foaming agent, has the functions of heat preservation, flame retarding, water prevention and corrosion resistance and the like, is unlikely to become yellow when in use, is safe and reliable, is excellent in performance, is good in compatibility with pigment dyestuff, is unlikely to damage the coated surface, is easy to modify, is nontoxic, is safe to use, does not pollute environment and is suitable for the fields of inner and outer wall coating, pipeline coating, wood furniture coating, decoration coating, chemical corrosion-proof coating and the like.

A preparing method of a ceramic-filled polytetrafluoroethylene microwave composite-medium substrate is disclosed. The method includes 1) adding silicon dioxide ceramic powder into a liquid mixture of hydrogen peroxide and concentrated hydrochloric acid after the silicon dioxide ceramic powder is dried, and heating the mixture to 50-70 DEG C to obtain a suspension; 2) subjecting the suspension to suction filtration and drying a product in a vacuum environment; 3) adding the silicon dioxide ceramic powder obtained in the step 2) into a solution mixture of deionized water and absolute alcohol, adjusting the pH value to be 3-5, weighing a coupling agent the weight of which is 1.0-2.5% of the weight of the silicon dioxide ceramic powder, performing ball milling, and fully mixing the mixture to obtain a material mixture; 4) filtering and drying the material mixture to obtain modified silicon dioxide ceramic powder; 5) ball-milling and mixing the modified silicon dioxide powder, chopped glass fibers and polytetrafluoroethylene, and then performing demulsification to obtain dough; and 6) subjecting the dough to molding and hot-pressed sintering. The ceramic-filled material prepared by the method has a low dielectric constant (with epsilon being equal to 2.94), ultralow dielectric loss (with tg[delta] being less than 0.0008, 10 GHz), low water absorption (less than 0.02%) and a small thermal expansion coefficient (less than 20 ppm/DEG C).

The application of the invention discloses a preparation method of a polypropylene nano composite material, which comprises the following steps of: (1) proportionally fusing and blending inorganic nano particles and maleic anhydride grafted polypropylene on an internal mixer, an open mill or a screw extruder to obtain a reinforcing agent master batch; (2) proportionally fusing and blending a beta crystal type nucleating agent and the maleic anhydride grafted polypropylene on the internal mixer, the open mill or the screw extruder to obtain a flexibilizer master batch; and (3) proportionally diluting and dispersing the reinforcing agent master batch and the flexibilizer master batch in a polypropylene high-polymer substrate, and carrying out injection molding to obtain the polypropylene nano composite material. With the preparation method, the technical problem that the nano particles and the nucleating agent agglomerate in the polypropylene substrate is well solved; when the flexibility of the modified polypropylene material is greatly improved, strength, rigidity, heat deflection temperature and other parameters are also improved to a certain extent, and simultaneously the density of the material is hardly increased so that a series of high-strength, high-flexibility and high-heat resistance modified polypropylene materials can be prepared.

The invention discloses a method for preparing silicon-aluminum aerogel by using fly ash as a raw material through normal pressure drying, which comprises the following steps of: mixing, grinding and calcining the fly ash and sodium carbonate to enable acidic oxides and amphoteric oxides in the fly ash to react with the sodium carbonate, then dissolving a sintered material with hydrochloric acid, and carrying out suction filtration to obtain a filtrate, i.e. silicon-aluminum sol; settling and aging the silicon-aluminum sol to form silicon-aluminum gel; soaking with circulating water to remove chloride ions; soaking with an ethanol solvent instead of water; soaking with an organosilicon compound as a surface hydrophobic agent for surface hydrophobic treatment; and preparing the silicon-aluminum aerogel through normal pressure drying. The invention uses the industrial waste fly ash as the raw material to replace an organosilicon source with high price and a certain toxicity, and uses normal pressure drying to replace supercritical drying, so the safety performance is greatly enhanced, the production cost is greatly lowered; and the method has simple process and convenient operation and is suitable for large-scale production. The prepared silicon-aluminum aerogel can be widely applied to the fields of heat insulating materials and the like.

The invention relates to an antistatic, halogen-free, and fire-retardant enhanced master batch dedicated for polyamide and a preparation method thereof. The fire-retardant master batch is composed of following components in parts by weight: 25 to 50 parts of PA, 15 to 30 parts of alkyl phosphinate fire-retardant, 15 to 30 parts of melamine polyphosphate fire retardant, 8 to 15 parts of zinc borate fire retardant, 4 to 6 parts of CTI improver, 1 to 1.5 parts of antistatic agent, 3 to 8 parts of flexibilizer, 0.5 to 1 part of coupling agent, 0.7 to 1.5 parts of lubricant, and 0.3 to 1 part of anti-oxidant. The sum of the weight ratio of components mentioned above is 100 wt%. The fire-retardant master batch is used to produce fire-retardant enhanced and modified nylon, meets standards of the United States underwriters laboratories (UL)-941.6mm and a higher V-0 grade, simultaneously achieves that glowing wire temperature (GWIT) is equal to or larger than 750 DEG C and the CTI value is equal to or larger than 600 V, also has a antistatic performance, meets European Union RoHS, International Electrotechnical Commission (IEC) halogen-free and Reach rule requirements, is easy to use and excellent in comprehensive performance, and does not affect color matching.

The present invention relates to a modified water-proofing asphalt roll material (called SA roll material for short), and is characterized by that in the raw material formula of asphalt 4-15% of thermoplastic elastomer polystyrene-butadiene-styrene block copolymer (SBS), 3-12% of atactic polypropylene (APP), 1-8% of light shielding agent, 0.05-3% of antioxidant, 0.05-3% of light stabilizer and 0.05-3% of UV absorbing agent. Said water-proofing roll material possesses low-temp. resistance, high-temp. resistance. UV-resisting property and good ageing resistance.

The invention provides a raw materials formula of enzymolysis lignin epoxy resin and its fabrication method. The formula includes enzymolysis lignin or its derivatives, bisphenol A-type compound, epichlorohydrin or its mixture with organic solvent, catalyst, curing agent, and filler. The preparation method includes adding enzymolysis lignin or its derivatives into epichlorohydrin solution or its mixture with organic solvent, stirring and adding catalyst, curing agent or the mixture of curing agent and filler, heating and reacting completely, vacuum-distilling to remove the excessive epichlorohydrin or organic solvent to obtain brown solid insoluble in water, washing, and drying to obtain enzymolysis lignin epoxy resin. The adopted enzymolysis lignin is the natural polymer material extracted from wood, bamboo and straw, which not only effectively use the biological resources, but also can replace petrochemical raw materials. The prepared enzymolysis lignin epoxy resin can be used for engineering materials, adhesives, coating or polymer materials modifier, which has a broad application prospect.

The invention discloses a preparation method of high-reinforcement modified anhydrous calcium sulfate crystal whiskers. The method comprises the following steps that: firstly, limestone powder is added into stirred water to be prepared into calcium salt aqueous emulsion; then, sulfuric acid and crystal modifiers are sequentially added into the stirred water to be prepared into sulfuric acid water solution; next, the calcium salt aqueous emulsion containing 1 mol part of Ca<2+> is added into the sulfuric acid water solution containing 2 mol parts of SO4<2-> with the temperature reaching 100 to 110 DEG C, then, morphology control agents are added, the materials are subjected to stirring and aging for 2 to 3.5 hours under the temperature condition being 110 to 120 DEG C, leaching and washing are carried out, and calcium sulfate hemihydrate crystal whisker wet products are obtained; the calcination drying finally is carried out under the temperature condition higher than 200 DEG C to obtain the anhydrous calcium sulfate crystal whiskers; and then, the surface modification treatment is carried out to finally obtain the high-reinforcement modified anhydrous calcium sulfate crystal whiskers. The preparation method has the advantages that the product quality is high, the cost is low, the preparation process is short, the reaction condition is mild, and in addition, green and environmental-friendly effects can be realized.

The invention provides a natural fiber crystal variation modified liquid medium filling and recovery system based on paralleled multiple buses and multiple modified kettles. The natural fiber crystal variation modified liquid medium filling and recovery system based on the paralleled multiple buses and multiple modified kettles comprises a liquid medium low-pressure mass flow liquid-filling bus, a liquid medium high-pressure small flow liquid-filling bus, a liquid medium low-pressure mass flow liquid-return bus, a liquid medium low-pressure small flow liquid-filling bus, a gas phase balance bus, and n modified kettles which are in parallel connection on the buses, and n >=1. The invention further provides a natural fiber crystal variation modified liquid medium filling and recovery method based on the paralleled multiple buses and multiple modified kettles. The liquid-filling process comprises mass flow balance liquid filling and small flow pressure boosting liquid filling, and the liquid return process comprises mass flow pressure relief liquid return, mass flow balance liquid return, small flow balance liquid return, and cage shift liquid exhaustion. The natural fiber crystal variation modified liquid medium filling and recovery system and the method based on paralleled multiple buses and multiple modified kettles are good in modified effect, small in system energy consumption, and high in production efficiency.

The invention relates to a preparation method for a solvent-based lignin-cyanamide derivative flame retardant. The method is characterized in that: after being subjected to a hydroxymethylation reaction, solvent-based lignin is subjected to a condensation polymerization with cyanamide and urea to prepare the solvent-based lignin-cyanamide derivative flame retardant. The solvent-based lignin-cyanamide derivative flame retardant has characteristics of high performance, halogen free, low cost, simple preparation method, and good flame-retardant effect, and can be widely applicable for the modified fields of polymers such as rubber, plastic and the like, and has good economic benefit and social benefit.

The invention relates to a compound modification method for clay, which comprises the following steps: dissolving 0.5-2g of silane coupling agent in a certain amount of alcohol-water mixture, and stirring for a certain time on a magnetic stirrer; adding a certain amount of clay into a stirring furnace, performing high-speed stirring at a certain temperature, and meanwhile, adding the alcohol-water mixture into the clay within a certain time; after the alcohol-water mixture is added, continuing to stir for 0.5 hour, pouring out, and performing heat treatment at 80-200 DEG C for 1-3 hours; and mixing the product obtained in the previous step with a certain amount of long-chain alkyl ammonium salt water solution, adding a small amount of acetic acid to regulate the pH value to 2-5, stirring at a certain temperature for a certain time, repeatedly performing vacuum filtration 2-5 times, and performing heat treatment at 80-200 DEG C for 2-5 hours. Secondary modification takes full advantages of the synergic modification effects of the silane coupling agent and the long-chain alkyl ammonium salt, enlarges the molecular layer interval of the clay, increases the affinity of the clay to polymer and widens the application range of the clay.