36results about How to "The production process is safe and controllable" patented technology

The invention provides a tissue engineering nerve graft based on a biological printing technology and a preparation method thereof. The tissue engineering nerve graft comprises an outer tube and a tube inside scaffolds, wherein trophic factors and / or cells can cover the inner surface and the outer surface. A high-fidelity printing operation is performed according to the actual nerve shape demand by utilizing the biological printing technology, a polymer solution is printed into the specified nerve graft in a three-dimensional way by using an ink-jet printer by adjusting the sizes and the quantity of the jet nozzles of the ink-jet printer, the distances from the jet nozzles to a bottom layer and the pulse frequency of a supercharger and writing a control program of specific printing, and the specified nerve graft is applied to treatment of peripheral nerve defect and spinal cord injury.

The invention discloses viscous porous granulated ammonium nitrate fuel oil explosive and a preparation method thereof. The ammonium nitrate fuel oil explosive comprises the following constituents in weight percent: 83 to 85 percent of porous granulated ammonium nitrate, 4.5 to 6 percent of compound oil phase, 3.5 to 6 percent of tackifier, 0.2 to 0.5 percent of expanded perlite, 1.3 to 2 percent of powder type explosive energy accelerant, and 3 to 5 percent of thickener. The method comprises the following steps: a, adding the porous granulated ammonium nitrate into a viscous porous granulated ammonium nitrate fuel oil explosive mixer, then adding the compound oil phase, stirring for 2 to 4 minutes at normal temperature, mixing the porous granulated ammonium nitrate and the compound oil phase to be uniform, so as to form mixture A; b, adding the tackifier, the powder type explosive energy accelerant and the expanded perlite into the mixture A, stirring for 1 to 2 munities at normal temperature, mixing the mixture A, the tackifier, the powder type explosive energy accelerant and the expanded perlite to be uniform, so as to form mixture B; and c, adding the thickener into the mixture B, stirring for 1 to 2 munities at normal temperature, and mixing the mixture B and the thickener to be uniform, so as to form the viscous porous granulated ammonium nitrate fuel oil explosive, and then packaging the viscous porous granulated ammonium nitrate fuel oil explosive. The viscous porous granulated ammonium nitrate fuel oil explosive and the method have the advantages that preparation and storage processes are safe and controllable, the power capability is high, the storage period is long, and the explosive is efficient and environmentally friendly.

The invention provides a preparation method and the application thereof for a cell-biological bracket compound based on biological print technology. The cell-biological compound is formed by fibrous protein which is drawn out from the autoblood of a patient and processed by an ink-jet print technology. The surface and the interior of the cell-biological compound encompass one or more trophic factors and bone mesenchymal stem cells derived from self. According to the invention, the biological print technology is adopted, the appearance shape, cells and encompassing state model of the trophic factors can be designed according to requirements and practical situation, the cell-biological bracket compound is obtained through printing accurately, the fibrous protein and the bone mesenchymal stem cells are derived from self, so that the problem of immunological rejection is avoided, the trophic factors are cultivated in the bracket and are released slowly with the degradation of the bracket material, the cell-biological compound is applied to the spinal cord injured part to promote nerve regeneration and functional reconstruction on the injured part.

The invention provides a continuous producing device of phosphorus pentafluoride, comprising a phosphorus single-substance closing silo, a spiral conveyer, a fluorine-phosphorus reactor, a cooling pipeline and a multi-grade filter. The continuous producing device of phosphorus pentafluoride is characterized in that the upper end of the spiral conveyer is connected to the lower end of the phosphorus single-substance closing silo, the tail end of the spiral conveyer is connected to the upper part of the fluorine-phosphorus reactor; one end of the fluorine-phosphorus reactor is connected with the cooling pipeline, and the other end of the cooling pipeline is connected with the multi-grade filter. The invention further provides a method for continuously producing phosphorus pentafluoride by using the device; the high-purity phosphorus pentafluoride gas is obtained by pre-reaction, continuous reaction, cooling and multi-grade filtering. According to the continuous producing device, the continuous production of phosphorus pentafluoride is realized; the continuous producing device has the advantages of being high in production efficiency, simple, safe and reliable in operation and good in product quality; the product purity can reach 99.8% above; therefore, the continuous producing device can be directly applied to the production of the lithium hexafluorophosphate.

The invention relates to the technical field of a polyurethane bonding agent, in particular to a single-ingredient solvent-free type polyurethane bonding agent, and a preparation method and application thereof. The single-ingredient solvent-free type polyurethane bonding agent is prepared from isocyanate terminated polyurethane prepolymers and optional additives; the isocyanate terminated polyurethane prepolymers are prepared from alcohol compounds containing reactive hydrogen and isocyanate through chain expansion reaction. The single-ingredient solvent-free type polyurethane bonding agent provided by the invention has the advantages that the raw materials can be easily obtained; the composition is simple; the production process is safe and controllable; good transparency, primary stickiness and bonding intensity are realized; the single-ingredient solvent-free type polyurethane bonding agent can be widely used in paper / plastic and paper / aluminum compounding.

The invention discloses a tissue engineering nerve graft with a suspension fiber scaffold. The nerve graft comprises a conduit and tube fiber scaffolds. The nerve graft is characterized in that a plurality of suspensions are arranged on each fiber scaffold along the fiber length direction, and are connected with the inner wall of the conduit; and the fiber scaffolds are distributed and suspended in the conduit by virtue of the suspensions. By utilizing bio-printing technology, built-in microfilaments of a tissue engineering nerve graft can be stably and uniformly distributed in the conduit by utilizing the supporting force of the suspensions, and each fiber scaffold has an independent space to guarantee that nerve cells can directionally grow along the fiber scaffolds and cannot have error bridging, so that the success rate of operations can be greatly improved.

The invention discloses a high-purity nickel-based high-temperature alloy and a preparation method of spherical powder of the high-purity nickel-based high-temperature alloy. The alloy comprises the following steps of selecting high-purity metal ingredients, smelting in a vacuum induction suspension smelting furnace, realizing pure smelting by controlling parameters such as smelting vacuum degree, refining temperature, time and the like, then pouring to obtain a steel ingot, and preparing the steel ingot into a bar; carrying out smelting, atomizing and powdering on the bar through EIGA and PREP technologies to obtain spherical metal powder; adopting vibrating screening and airflow classification, and classifying spherical powder under the protection of inert gas. According to the method, the content of nonmetal impurities is effectively controlled through raw material smelting control, atomization process control and post-treatment control, so that chemical elements of the powder have extremely high purity, and the high-purity high-temperature alloy spherical powder is not prone to generating cracks and other defects in the subsequent laser additive printing and laser cladding process and is good in binding force, high in strength, good in toughness and good in mechanical property, and the powder can be used for repairing high-end parts.

The invention discloses impact polystyrene with the capacity scale of 50,000 tons or above as well as equipment and a production process of the impact polystyrene. More than 90% of the components of the rubber modified polystyrene product are represented by the formula, n is the polymerization degree, the range of n is 600-7000, and n is different along with different types of products; in addition to the main components, the rubber composition also contains 3-10% of butadiene rubber for modification, 0-7% of white oil, 0-1% of an additive of stearate, and a small amount of an organic residue such as a monomer (the total amount is 800 ppm or less). The modified polystyrene has good impact strength, the vicat softening point is 92-106 DEG C, the tensile strength of the modified polystyrene is 22-45 MPa at normal temperature, and the modified polystyrene is a thermoplastic material with good toughness. No process waste water is generated in the production process, all the raw materials are recycled, a small amount of generated process waste gas reaches the standard and is discharged after being subjected to condensation and adsorption treatment of special equipment, and the good environment-friendly, energy-saving and consumption-reducing effects can be achieved.

The invention relates to the field of styrene-acrylic emulsions and provides a starch-base styrene-acrylic emulsion and a preparation method thereof. The starch-base styrene-acrylic emulsion containsthe following components in percentage by mass: 10%-30% of anionic starch and a derivative of the anionic starch, 0.5%-1.5% of vegetable gum, 10%-30% of a monomer mixture, 0.2%-1.0% of an initiator, 0.5%-3% of an inner cross-linking agent, 0.1%-3% of an outer cross-linking agent, and 40%-70% of water. The preparation method comprises the following steps: mixing the anionic starch and the vegetablegum, heating for decoction, cooling, dropwise adding the monomer mixture, the initiator and the inner cross-linking agent, maintaining the temperature, and adjusting the pH value to 6-8; and coolingto the temperature below 60 DEG C, adding the outer cross-linking agent for generate cross-linking reaction, cooling, and filtering. According to the preparation method, the tenacity of the starch-base styrene-acrylic emulsion is improved, little bubble is produced in the preparation process, the production process is safe and controllable, and the prepared starch-base styrene-acrylic emulsion ishigh in bonding strength, good in tenacity, elasticity and water tolerance and low in cost.

The invention discloses a light heat-insulation noise-reduction SiO2 aerogel material and a preparation method thereof, and belongs to the technical field of high-performance porous materials. The preparation method comprises the following steps: carrying out an acid-base two-step method and standing replacement on a trifunctional silicon source and a cationic surfactant in a water solvent to obtain an aerogel material; wherein the molecule of the trifunctional silicon source comprises a non-polar group which does not participate in hydrolytic condensation and three alkoxy groups which participate in the hydrolytic condensation. In the preparation method designed by the invention, water is used as a solvent, a surfactant is added to reduce the surface tension of the solvent, and an ordered assembly is formed in an aqueous solution to provide a micro-reaction container for a hydrophobic trifunctional silicon source; therefore, the prepared SiO2 aerogel material has the advantages of low density, low heat conductivity coefficient, high transparency and the like.

The coenzyme Q10 synthesizing process with coenzyme Q0 hydroquinone and isodecyl alcohol deca-isopentyl alcohol of purity not lower than 95 % as material includes dewatering and condensation reaction at room temperature under the catalysis of trifluoro methane sulfonic acid in no oxygen environment to obtain coenzyme Q10 hydroquinone, the oxidation of the reacted product without passing through any treatment with hydrogen peroxide and water solution of ferric trichloride to obtain crude coenzyme Q10 product, and crystallization of the crude coenzyme Q10 product in acetone to obtain yellow coenzyme Q10 product powder in content over 99 % and yield over 65 %. The present invention has simple operation, easy purification of the product, high yield, mild reaction condition, safe and controllable production process and industrial production value.

The invention relates to a cool / hot double-pipeline visible safety device for a biological fermentation tank, belonging to the technical field of beer fermentation equipment. The technical scheme is as follows: the cool / hot double-pipeline visible safety device comprises a pressure meter, a hot water pipeline valve A, a cooling medium pipeline valve A, a sight glass sheet A, a sight glass A, a filter screen A, a silica gel sealing gasket A, a movable joint A, a movable joint B, a safety valve, a movable joint C, a movable joint D, a hot water pipeline valve B, a cooling medium pipeline valve B, a sight glass sheet B, a sight glass B, a filter screen B, a silica gel sealing gasket B, a fermentation tank jacket and a temperature indicating meter. In order to heat or cool the fermentation tank, the cooling medium or hot water pipeline valve is closed, and the hot water or cooling medium pipeline valve is opened; and the hot water or cooling medium heats or cools the fermentation tank through the hot water or cooling medium pipeline valve, sight glass and fermentation tank jacket. In the heating or cooling process, the flow state of the hot water or cooling medium can be observed through the sight glass, the pressure meter displays the pressure of the pipelines and jacket, and the pressure can be automatically relieved under the condition of overpressure, thereby ensuring the safe and controllable production process.

The invention discloses a preparation method of 1H-1, 2, 3-triazole. The preparation method comprises the following step: performing a reaction on a compound A and sodium nitrite in a solvent I, wherein the compound A is 1,2-diamido-ethylene, 1,2-diamido-ethylene salt or a mixture of 1,2-diamido-ethylene and 1,2-diamido-ethylene salt. Compared with the prior art, the preparation method has the beneficial effects that (1) a production line is short, the conversion rate of a target product is high, the utilization ratio of atoms is high, and the atom economy is high; (2) the molar yield is high, and the total molar yield is above 90%; (3) the solvent can be recycled and reused, and the discharge amount of waste water is very small; and (4) a production process is safe and controllable.

The invention discloses transparent polystyrene with the capacity scale of 50,000 tons or above as well as production equipment and process of the transparent polystyrene. The main component of the obtained transparent polystyrene product is as follows: n is the degree of polymerization, and the range of the n is 600-7000, and the n is different along with different types of products. The transparent polystyrene has good transparency, the Vicat softening point is 85-106 DEG C, the tensile strength of the transparent polystyrene is 40-55 Mpa at normal temperature, and the transparent polystyrene is a thermoplastic material. The molecular structure contains a small amount of macromolecules with a special structure, and a considerable amount of hydrocarbon micromolecules are contained in gaps of the macromolecules, so that certain slippage can be generated among the macromolecules, and the material has good transparency and mechanical properties compared with products obtained by other process production methods. The process waste water is basically not generated in the production process, all the raw materials are recycled, a small amount of generated process waste gas reaches the standard and is discharged after being condensed and adsorbed by special equipment, and good environment-friendly, energy-saving and consumption-reducing effects can be achieved.

The invention relates to a method for preparing a lithium iron phosphate cathode material at low cost and an application of the lithium iron phosphate cathode material in a lithium ion battery. The preparation method comprises the following steps: firstly, introducing aqueous solutions of a lithium source and a phosphorus source into a spray drying cavity at a certain flow rate by an industrial spray drying method, and enabling the two substances to quickly react at relatively high surface energy at 140-220 DEG C, so as to prepare an iron phosphate material; then respectively preparing a lithium source solution, a reducing agent solution and an iron phosphate turbid liquid; under the conditions of normal temperature and constant-speed stirring, respectively injecting the lithium source solution and the reducing agent solution into a reaction kettle filled with iron phosphate turbid liquid, performing stirring for 2-3 hours at a constant speed, and centrifuging, washing and drying a product after the reaction is finished to obtain the lithium iron phosphate material. The synthesis process is carried out at 220 DEG C or below, and inert gas shielding is not needed; the whole processis operated in air, so the operation is safe, easy and convenient, the repeatability is good, the preparation cost of the target product is low, and the method has important significance in practicalapplication.

The invention discloses a treatment method for waste gas generated in the process of producing epoxy chloropropane through chloropropene epoxidation. The method comprises the following steps: treatingwaste gas generated in the process of preparing epoxy chloropropane through epoxidation reaction of a reaction control phase transfer catalyst, hydrogen peroxide and chloropropene, wherein the wastegas contains nitrogen, oxygen, chloropropene and water vapor; the nitrogen is added into a gas-phase buffer tank (V1)at the top of a reactor (R1)to dilute tail gas, the diluted tail gas passes througha first-stage condenser (E1), a second-stage condenser (E2)and a third-stage condenser (E3)to recover condensed chloropropene and condensate water and then enters a membrane filter (M1)to filter a chloropropene-containing gas, and the chloropropene-containing gas is compressed to recover the chloropropene; an inorganic matter-containing gas filtered by the membrane filter (M1)is condensed by a four-stage condenser (E4)to recover trace chloropropene in the inorganic matter-containing gas so as to reach the emission standard.

A device for producing expandable polystyrene by a bulk method comprises a polymerization reaction unit which is connected with a heating devolatilization device through a discharge pump; the upper end of the heating devolatilization device is connected with a condenser and a vacuum liquid collection tank; and the lower part of the heating devolatilization device is connected with a mixer, a melt heat exchanger, a pump and a high-pressure underwater pelletizing system through a pump. The device can be used for producing flame-retardant expandable polystyrene (EPS) and can also be used for producing graphite expandable polystyrene (EPS). The materials in the polymerization reaction unit comprise the following components in parts by weight: 80-95 kg of styrene, 2-10 kg of a solvent and 0.5-8 kg of an auxiliary agent. The particle size of the obtained expandable polystyrene EPS ranges from 0.7 mm to 1.0 mm, residual monomers are low, waste water is little, and the environment-friendly effect is good.

The invention belongs to the technical field of organic synthetic chemistry, and particularly relates to a metal complex and a preparation method thereof. The general molecular structural formula of the metal complex is shown as formula I in the specification. The metal complex is a complex formed by complexing a chiral phosphorus-sulfur compound and metal, has a typical high-functionalization structure, such as a chiral quaternary carbon atom containing an electron withdrawing group and an amino group, not only has a classical organic metal complex structure, but also widens the coordinationof the phosphorus-sulfur compound, can expand organic asymmetric catalytic reaction, and has good application in synthesis of drug intermediates and preparation of functional materials.

A low-energy-consumption device for producing expanded polystyrene through a bulk method comprises a polymerization reactor (1), the lower end of the polymerization reactor (1) is connected with a mixer (5) through a discharging pump (4), and then the polymerization reactor (1) is sequentially connected with a plug flow reactor (6), a static mixer (7), a plug flow reactor (8), a pump (9) and a high-pressure underwater pelletizing system (10) through pipelines. When the front end of the mixer (5) is provided with an interface for adding a molten flame retardant master batch, flame-retardant expandable polystyrene (EPS) can be produced; when the front end of the mixer (5) is provided with an interface for adding molten graphite master batches, graphite expandable polystyrene (EPS) can be produced. The size of the obtained expanded polystyrene particles can be strictly controlled between 0.7 mm and 1.0 mm, the expanded polystyrene particles have good impact resistance and tensile strength, and the unit energy consumption is reduced to one third.

The invention discloses an industrial-scale high-performance high-impact polystyrene production device and a production process. A pre-polymerization reaction device in the production device is a pre-polymerization reaction kettle group which is formed by combining four full mixing flow reaction kettles with stirring in a specific series-parallel connection manner; the prepolymerization reaction kettle group comprises two groups of parallel two-stage prepolymerization kettles, and each group of two-stage prepolymerization kettles consists of a first-stage prepolymerization kettle and a second-stage prepolymerization kettle which are connected in series. The production process is a styrene and rubber mixed solution graft copolymerization reaction process formed by combining four prepolymerization kettles; in the prepolymerization reaction, two groups of parallel two-stage prepolymerization kettles are adopted for feeding at the same time; by controlling different process conditions of each group of kettles, the reaction of each group of two-stage prepolymerization kettles reaches the styrene reaction conversion rate and the rubber grafting rate which meet specific requirements; and mixing the two groups of materials in a plug flow reactor, and further polymerizing to obtain the dispersed phase particle modified high-performance high-impact polystyrene with a submicrostructure with specific particle size and particle size distribution.