233results about How to "High apparent density" patented technology

The invention relates to aqueous polyurethane superfine fiber synthetic leather and a preparation method thereof. The preparation method comprises the following steps of: firstly, adding the following components according to parts by weight, i.e. 2-5 parts of foaming agents, 50-200 parts of water, 2-3 parts of foam stabilizers and 0-3 parts of waterborne colorants, into 100 parts of aqueous anionic polyurethane dipping sizing agents, and stirring the components and the sizing agents uniformly at high speed by using a blender so as to prepare a sizing agent; secondly, dipping non-woven fabricsin the sizing agent, scrapping the surface of the fabrics and keeping partial cells; thirdly, solidifying aqueous polyurethane on the dipped non-woven fabrics through aqueous coagulating liquid so asto form cells; fourthly, carrying out water scrubbing after aqueous polyurethane resin is completely solidified, and drying the aqueous polyurethane resin by an infrared drying oven so as to obtain base cloth; fifthly, treating the dried base cloth through an alkali reducing process; sixthly, treating the base cloth treated through the alkali reducing process through an postprocessing process; and seventhly, preparing the obtained base cloth into the synthetic leather. The aqueous polyurethane superfine fiber synthetic leather is prepared by the method.

Disclosed is a fine-fibers-dispersed nonwoven fabric comprising dispersed fine fibers having a fiber diameter of 4 μm or less and a fiber length of 3 mm or less, wherein an adhesion rate of substances adhered to the nonwoven fabric is 0.5 mass % or less. Further, a process and an apparatus for manufacturing the fine-fibers-dispersed nonwoven fabric, as well as a sheet material comprising the fine-fibers-dispersed nonwoven fabric are also disclosed.

The invention relates to recycled concrete and a preparation method thereof, and belongs to the technical field of concrete. The recycled concrete comprises (by weight): 150-280 parts of cement, 90-130 parts of water, 800-950 parts of modified recycled coarse aggregate, 400-530 parts of fine aggregate, 40-85 parts of fly ash, 80-100 parts of mineral powder, 50-140 parts of zeolite powder, 30-60 parts of epoxy resin, 4-10 parts of a water reducing agent and 2-6 parts of an air entraining agent. The preparation method of the modified recycled coarse aggregate comprises the following steps: S1, crushing and screening waste concrete to obtain recycled coarse aggregate; S2, soaking the recycled coarse aggregate obtained in the step S1 in an acetic acid solution with the mass concentration of 2-7%, and airing; S3, stirring 80-110 parts of polyvinyl alcohol, 60-110 parts of silica fume, 40-80 parts of sodium silicate and 800-1,000 parts of water to obtain a modified liquid; and S4, soaking the recycled coarse aggregate obtained in the step S2 in the modified liquid obtained in the step S3, taking out the soaked recycled coarse aggregate, and baking the recycled coarse aggregate to obtainthe modified recycled coarse aggregate. The recycled concrete provided by the invention has a good compressive strength effect.

The invention relates to a powder material preparation method, in particular to a method for preparing fine spherical tungsten powder. Plasma parameters are adjusted by building a stable argon plasma, thereby heating tungsten powder material and acquiring the fine spherical tungsten powder through the separation after cooling and solidification, and the obtained tungsten powder has better fluidity, higher density, purity and particle cleanliness of surface, and lower powder particle porosity compared with the tungsten original powder; and the method has advantages of changing shapes of tungsten powder particles, high sphericity, increasing the apparent density of powder, improving the tungsten powder fluidity and physical characteristics of the tungsten powder, and reducing costs.

The invention relates to an ardealite-based high-strength light building block prepared from ardealite and a production process thereof. The ardealite-based high-strength light building block is prepared from the following raw material components by weight percent: 50-70% of dry basis of alpha high-strength gypsum, 3-10% of cement, 10-20% of coal ash, 10-20% of glass beads and 0.1-0.4% of air entraining agent. The raw materials are mixed together evenly in a water-material ratio from 0.4 to 0.6 and stirred into slurry; then the slurry is moulded to form the ardealite-based high-strength light building block. The ardealite-based high-strength light building block produced through the production process provided by the invention is found by detection that the apparent density of the solid building block is not higher than 1000 kg/m<3>, the strength grade is above MU10, the softening coefficient is not lower than 0.6 and the utilization rate of the solid waste is more than 70%.

There are provided reactive metal powder atomization manufacturing processes. For example, such processes include providing a heated metal source and contact the heated metal source with at least one additive gas while carrying out the atomization process. Such processes provide raw reactive metal powder having improved flowability. The at least one additive gas can be mixed together with an atomization gas to obtain an atomization mixture, and the heated metal source can be contacted with the atomization mixture while carrying out the atomization process. Reactive metal powder spheroidization manufacturing processes are also provided.

The invention provides a method for producing vanadium-nitrogen alloy. In the method, powdered vanadium oxide or ammonium metavanadate, carbon powder, bonding agents and density increasing agents are evenly mixed and are subjected to briquetting and forming; the mixture is continuously added in an external-heat type rotary kiln under the atmosphere of nitrogen gas and preheated up to the temperature of below 1,000 DEG C under the protection of the nitrogen gas, and at a discharge port, preheated massive products which are cooled down to the room temperature under the protection of nitrogen gas are collected; and the massive products are put in an improved soft magnetism nitrogen atmosphere kiln and heated up to the temperature of between 1,000 and 1,500 DEG C so as to make materials carry out the carbonization reaction and the nitriding reaction, and the vanadium-nitrogen alloy products are obtained after discharge. In the vanadium-nitrogen alloy obtained, the V content is between 78 and 83 percent, the N content is between16 and 21 percent, the C content is less than or equal to 6 percent max, the contents of silicon, phosphor and aluminum are less than 0.01 percent, and the apparent density is more than 4.4g/cm<3>. The apparent density can be adjusted according to the requirements of a customer, and the maximum apparent density is 5.0 g/cm<3>. The method is characterized in that under the condition of not changing prior production processes, the apparent density of the vanadium-nitrogen alloy is improved by adding the density increasing agents, and the adsorption rate of molten steel in the vanadium-nitrogen alloy is more than 98 percent.

The freeze forming preparation process of ternary lithium ceramic microsphere includes the following steps: mixing the material for ternary lithium ceramic microsphere, high molecular adhesive and solvent, mixing in a ball mill to form suspension slurry and defoaming; dropping the slurry into cooling medium to form microsphere in a microsphere forming unit, and low temperature vacuum drying in a freezing drier to form ceramic microsphere precursor; roasting, calcining and sintering; and programmed heat treatment to obtain ternary lithium ceramic microsphere. The ternary lithium ceramic microsphere has high sphericity, controllable size, high size dispersivity, high apparent density, high phase purity, high strength and other features.

A process for polymerizing polyethylene with chromium-based catalysts wherein one or more supported chromium-based catalysts is mixed with mineral oil to form a slurry and the slurry is then introduced into a polymerization reactor, especially a gas-phase polymerization reactor.

The invention relates to size and a method for treating recycled coarse aggregates, and belongs to the field of concrete recycled aggregates treating agents and concrete recycled aggregates treating. In order to solve the technical defects that the strength of the recycled coarse aggregates is low due to high water absorption and large porosity, the invention provides the size and the method for treating the recycled coarse aggregates. The size for treating the recycled coarse aggregates comprises sulphoaluminate cement, admixtures and water. The sulphoaluminate cement of the size permeates into the recycled coarse aggregates, so that the microcracks generated in recycled coarse aggregates crushing are filled to a certain degree; meanwhile, through the use of the dilution and nucleation effects of the admixtures and Ca(OH)2 enriched in old mortar of the recycled coarse aggregates consumed in secondary hydration reaction, the mortar structures of the recycled coarse aggregates are improved, so that the strength of the waste concrete recycled coarse aggregates is improved. After the size and the method are adopted, the crush indexes of the recycled coarse aggregates are remarkably reduced and meet the requirement regulated Pebble and crushed stone for construction GB/T14685-2011.

The invention relates to a method for preparing a catalytic cracking catalyst, which comprises the following steps: (1) weighting zeolite, a binder precursor, a substrate precursor and a pulpable intermediate; (2) forming a solid-liquid slurry containing the zeolite, the binder precursor, the substrate and the pulpable intermediate; (3) stirring and/or grinding the slurry, performing a uniform mixing and uniformization to the above components to realize the refinement of particle size; (4) converting catalyst slurry into molded particles, and converting the molded catalyst particles into a catalyst finished product by drying or calcinating. The solid content in the catalyst formula is 30%-65%, the addition of the solid content enables a great addition to the apparent density of the catalyst, the addition of the catalyst bulk density enables a close association with the enhancement of the wearing performance, accordingly, the addition of the catalyst bulk density is capable of reducing the volume load of the catalyst or filling more catalyst in a given volume of a reactor.

The invention discloses a method for preparing hybrid fiber modified light water-permeable and durable recycled concrete. First a mineral miscellaneous material, a cementing material and a modified regenerated coarse aggregate are evenly mixed, water is poured for stirring to obtain cement paste, a ternary hybrid fiber and water are evenly mixed and then poured into the cement paste for stirring,and an efficient naphthalene water reducer is added; after uniform mixing, foams well made by a foaming device are added, and full and uniform mixing is performed to obtain concrete slurry; the well prepared concrete slurry is poured into a die and lightly and evenly vibrated, the surface of a poured sample is covered with a preservative film, demolding is performed after standing, and curing is performed. A glass fiber, a polypropylene fiber and a steel fiber are mixed into the ternary hybrid fiber, the recycled concrete is modified, the compressive strength can be obviously improved, the steel fiber in the hybrid fiber belongs to high elastic modulus fibers, so that the elasticity modulus of the recycled concrete after the doping of the hybrid fiber is increased, and the doping of the hybrid fiber can obviously improve the vibration resistance of the recycled concrete and enhance ductility and energy dissipation performance of the recycled concrete.

Provided is a cable-shaped alkali metal-sulfur battery comprising: (a) a first electrode comprising an electrically conductive porous rod and a first mixture of a first electrode active material and a first electrolyte residing in pores of the porous rod; (b) a porous separator wrapping around the first electrode; (c) a second electrode comprising an electrically conductive porous layer wrapping around or encasing the separator, wherein the porous layer contains a second mixture of a second electrode active material and a second electrolyte residing in pores of the porous layer; and (d) a protective sheath encasing the second electrode; wherein one electrode is a cathode containing sulfur, a sulfur-carbon compound, sulfur-polymer composite, or metal sulfide.

The invention provides a good mattress capable of preventing dewing and dispensing, characterized in that: the thermal plasticity resin as the raw material or the main raw material melts to be extruded into lines and a large amount of lines are wounded out of order and welded into annular aggregates of the lines and the aggregates are formed into the plate-like shape and then cooled and solidified, therefore a three-dimensional net structure is formed. The left, right relatively-long side-surfaces have side-surface firmness parts with high apparent density.

The invention discloses a preparation method of an oxidized graphene/sodium lignin sulfonate modified polyurethane foam material, relates to the preparation method of materials, and aims to solve theproblems of poor compatibility between graphene and a polyurethane monomer and poor dispersity of oxidized graphene in a polyurethane foam material. A method I comprises the following steps: liquidifying a sodium lignin sulfonate solvent; 2, modifying the oxidized graphene; 3, preparing a polyhydroxy component; 4, preparing an isocyanate component for foaming; 5, foaming. A method II comprises thefollowing steps: 1, liquidifying the sodium lignin sulfonate solvent; 2, modifying the oxidized graphene; 3, preparing the polyhydroxy component; 4, foaming. According to the preparation method disclosed by the invention, MDI (Diphenylmethane Diisocyanate)/sodium lignin sulfonate can be utilized for modifying the oxidized graphene, the modified oxidized graphene can be uniformly and stably dispersed in a base material, the modified oxidized graphene and connected sodium lignin sulfonate molecules or MDI are used as a whole, and the problem of compatibility of an inorganic additive-oxidized graphene in a polymer matrix is solved.

The invention belongs to the technical field of silicon dioxide, and particularly relates to a preparation method of silicon dioxide for low-specific-surface-area high-density thickening type toothpaste. The silicon dioxide for the low-specific-surface-area high-density thickening type toothpaste is prepared by the following steps: taking a sodium sulfate solution with the mass concentration of 10-12% as a mother solution, dripping a sodium silicate solution with the molar concentration of 1.25-1.5 mol/L and a sulfuric acid solution with the molar concentration of 6-7mol/L at the same time, and carrying out a reaction at a segmented temperature and a segmented pH value. When the silicon dioxide for the thickening type toothpaste prepared by the preparation method provided by the inventionis applied to the preparation process of the toothpaste, the time can be shortened, the dust can be reduced, the cost can be saved in the transportation process, and the cleaning effect of the toothpaste cannot be reduced when the silicon dioxide is compounded with the friction type silicon dioxide in the toothpaste body.