750results about How to "Strong force" patented technology

An artificial disc having a pair of opposing plates for seating against opposing vertebral bone surfaces, separated by at least one spring mechanism. The preferred spring mechanism is at least one spirally slotted belleville washer, and in some embodiments the belleville washer is also radially thinning or thickening. Various illustrated embodiments use two washers or one washer. For double washer embodiments, the wide ends of the washers seat against respective opposing plates, in some embodiments each being maintained thereagainst by a retaining wall and ring or a circular recess and retaining shield. For single washer embodiments, the narrow end of the washer can be modified to have a curvate socket for rotatably mounting onto a semispherical protuberance extending from one of the plates.

An artificial disc having a pair of opposing plates for seating against opposing vertebral bone surfaces, separated by a spider spring having a plurality of spring arms extending radially from a central hub. Various spring arm embodiments disclosed include spring arms that are straight, bowed, grooved, wavy, thinning, or thickening; and spring arms with parallel sides, radially outwardly diverging sides, or radially outwardly diverging and curving sides. Various spider spring embodiments disclosed include spider springs with central hubs that are solid, bored, have curvate sockets, or have semispherical protuberances. Various plate embodiments disclosed include plates having, on inwardly facing surfaces, a curvate socket, a semispherical protuberance, a circular recess, or a flat surface. The spider springs are disposable between the plates, through various disclosed couplings, so that the plates compress, rotate and angulate freely relative to one another, enabling the artificial disc to mimic a healthy natural intervertebral disc.

This invention discloses a method for synthesizing organic-inorganic bentonite composite. The method comprises: utilizing bentonite as the main material, performing inorganic modification through cation-exchange reaction by using hydroxyl aluminum aqueous solution, torrefying to obtain hydroxyl-containing aluminum-pillared bentonite with high porosity and high specific surface area, and reacting between the hydroxyls and silylation agent to graft silane groups onto aluminum-pillared bentonite and obtain organic-inorganic bentonite composite. The organic-inorganic bentonite composite has both the advantages of inorganic pillared bentonite such as high porosity and high specific surface area, and those of organic bentonite such as high organic carbon content and high hydrophobicity thus can be used to treat organic waste gases and wastewater with a good effect by surface adsorption as well as distribution.

There is provided a chair that realizes a state preferably following a motion of a sitter in accordance with a posture of the relevant sitter, and a state preferably supporting the sitter. The chair includes a lower frame portion supported so as to be capable of rocking between a standing position and a rearward tilting position with respect to a base, and an upper frame portion supported so as to be capable of rocking between a normal position and a rear end position with respect to the relevant lower frame portion. Furthermore, upper frame portion biasing means that elastically biases the upper frame portion from the rear end position to the normal position is provided. This upper frame portion biasing means is adapted to change an elastically biasing force to the upper frame portion corresponding to a position in the rocking movement of the lower frame portion.

A sealed container lid of a vacuum valve operation type is provided, in which an engagement structure of a silicon packing is simple, and a relatively strong sealing force is obtained. A process for engaging or disengaging a lid to a container body may be performed based one-touch method. The sealed contained lid of a vacuum valve operation type comprises a body which is injection-molded and has a circular groove formed in a horizontally and outwardly opened shape for an engagement of the silicon packing, and a downwardly bent peripheral part which is formed at an outer peripheral part of the body based on a double injection method while surrounding the same.

A light extraction substrate for an electroluminescent device and a manufacturing method thereof, in which light extraction efficiency is increased. The light extraction substrate for an electroluminescent device includes a substrate and a light extraction layer formed on the substrate. The light extraction layer contains an oxide that has a wide band gap of 2.8 eV or more. The light extraction layer has a texture on the surface thereof.

The invention discloses a preparation method of a polyacrylamide emulsion. The preparation method comprises the following steps of adding acrylamide, one or more anion monomers, a grafting matrix, an aqueous stabilizer, a molecular weight conditioning agent and an initiator into water, adjusting a pH value to obtain a water phase, adding an emulsifier into a hydrocarbon solvent to obtain an oil phase, dropwisely adding the water phase into the oil phase, carrying out one-step emulsification or multistep emulsification to obtain an emulsion, carrying out displacement deoxygenation on the emulsion by inert gas, and adding the initiator into the emulsion for polymerization initiation to obtain a branched anion polyacrylamide water-in-oil anti-phase emulsion after polymerization is finished. The polyacrylamide emulsion obtained by the preparation method is used for the modern papermaking industry, avoids inorganic filler re-falling after retention, improves inorganic filler actual retention effects, avoids falling-off of dust and lint of a screen cloth, guarantees uniform and stable retention of an inorganic filler in a page, and properly reduces a bentonite use amount.

The invention relates to a method for preparing magnetic silicon dioxide microspheres with the surfaces chelated with metal ions; the method of the inventioncomprises the following steps of preparation of the magnetic silicon dioxide microspheres, epoxidation of the magnetic silicon dioxide microspheres, carboxylation of the magnetic silicon dioxide microspheres and chelation technique of metal ions. Compared with the existing preparing method, the method of the invention has the advantages of reasonable design, simple operation and large amount of chelation of metal, etc. The magnetic silicon dioxide microspheres with the surfaces chelated with the metal ions, which are prepared by adopting the method, contain cobalt ions, have stronger bonding force with the modified microspheres so as to lead the cobalt ions to be not easy to leak out, and have higher selectivity and proper bonding strength with histidine on the protein, thus leading the magnetic silicon dioxide microspheres with the surfaces chelated with the metal ions to have high selectivity to hexameric histidine tag protein, and being easy to realize the separation and the purification of the target protein; the magnetic silicon dioxide microspheres with the surfaces chelated with the metal ions, which are prepared by adopting the method, can be used for separating the hexameric histidine tag protein.

The invention discloses a copolymer with temperature resistance and water solubility and the preparation method and application thereof, which is characterized in that: 20 portions of acrylic amide, 0.1 to 10 portions of anion monomer or/and cation monomer, 0.05 to 3 portions of fluorine-containing styrene or/and perfluoroalkyl styrene hydrophobic monomer, 0.5 to 60 portions of surface active agent and 50 to 700 portions of deionized water are put into a three-necked reaction bulb; after the solution pH is regulated to be equal to 2.5 to 9 and N2 is connected for 30 minutes, 0.001 to 0.2 portion of an evocating agent of persulfate is added under temperature of 20 to 70 DEG C, reacting for 6 to 36 hours, and PATF is prepared. Then water is used for diluting so as to prepare PATF concentrated solution, thus obtaining a copolymer that has medium molecular weight and water solubility, is high-temperature resistant, has an ability of molecular association and can be used in high temperature and high salinity reservoir. The copolymer is prepared into aqueous solution with a mass concentration of 0.3 to 3g/L and a surface-active-agent concentration of 0.01 to 4mmol/L, which is put in a blending container with a dasher and is stirred even at room temperature to prepare a polymer oil-displacing agent which is high-temperature resistant, high tackifying and anti-sharing and has excellent aging resistance under high salinity and the temperature of 110 DEG C. The prepared oil-displacing polymer has excellent solution properties owing to the supermolecular structure formed by the association between molecules of fluorine-containing cinnamene or/and alkylbenzene hydrophobic groups, thus having favorable application prospects in high temperature and high salinity reservoir exploitation.

It is an object of the present invention to provide a convenient groin protector for combat sports capable of reliably preventing the position of the plate-like rigid body of the groin protector body from being deviated during a match, and capable of wearing and taking off the groin protector in a short time. The groin protector comprises, for wearing the protector body, a waist belt made of inelastic band-like member which is attached such that the plate-like rigid body 1 is suspended and which is wound around and attached to a hip of the player M, and a surface fastener type belt retaining mechanism 3 which retains so that the waist belt 2 is not loosened in a state in which the waist belt 2 is wound around the hip of the player M and fastened.

The invention discloses a CsPW/Zr-MCM-41 catalyst prepared in a supercritical CO2 environment. The preparation method comprises the following steps: Zr-MCM-41 is taken as the carrier, and 10-60% of Cs modified salts is loaded by adopting the supercritical CO2 impregnation technology; with the utilization of the catalyst, the glycerin conversion rate reaches 65.2-100%, the acrolein selectivity reaches 56.8-85.4%; the invention further discloses application of the CsPW/Zr-MCM-41 catalyst to preparation of acrolein through glycerol selective dehydration. Compared with the prior art, the catalyst prepared by adopting the preparation method has the advantages that the dispersion degree of Cs modified salt on the carrier is high, the acting force between the Cs modified salt and the carrier is strong, the hydrothermal stability is high, the acidity loss possibility is low, and meanwhile, when compared with the conventional product, the obtained product is high in glycerin conversion rate and acrolein selectivity, and long in service life.

The invention discloses a novel method for modifying graphene with polymer. By introducing polydopamine and combining covalent modification with non-covalent modification, the method increases the stability of the modified product structure under the premise of ensuring the integrity of the graphene structure. Firstly, by utilizing the strong adhesion of dopamine, the dopamine is self-polymerized to form a film on the surface of a graphene sheet, moreover, 2-Bromo-2-methylpropionyl bromide (BiBB) as common initiator for atom transfer radical polymerization (ATRP) is grafted on the dopamine by amidation, at the same time, graphene oxide (GO) is partially reduced by the dopamine (DA), and thereby graphene macroinitiator RGO@PDA-Br is obtained. Polymeric monomer is then added, so that the ATRP of the polymeric monomer is initiated on the surface of the graphene, and thereby a polymer-modified graphene material is obtained. By controlling conditions such as monomer concentration and reaction time, the novel method can obtain modified graphene materials with different densities and chain lengths of polymer grafted on the surfaces, meeting the characteristics of controllable/living ATRP. In addition, the feasibility and universality of the novel method for modifying graphene with polymer put forward by the invention are applicable to various monomers suitable for ATRP.

The invention provides a fluorescent probe represented by the formula (I), wherein R1 and R2 are independently selected from H or an aromatic vinyl group, and at least one of R1 and R2 is the aromatic vinyl group; R3 is selected from H, F, Cl, Br, OH, OCH3, N(CH3)2 or C1-C6 alkyl; and R4 is selected from C1-C6 alkyl. Compared with the prior art, because the fluorescent probe provided by the invention has a relatively large electronic conjugated system and plane, the intensity of the intramolecular charge transfer effect can affect the molecular fluorescence emission intensity; when the fluorescent probe and the G-quadruplex generate a specific action, the flexibility of intramolecular rotatable double bonds is restricted, the intramolecular charge transfer effect is enhanced, and the fluorescence is also enhanced significantly; moreover, the fluorescent probe provided by the invention has the advantages of low biotoxicity, phototoxicity and photobleaching property, good light stability, good water solubility and good cell membrane permeability.

The invention discloses a propane dehydrogenation catalyst, which is obtained by loading metal platinum on magnesium aluminate spinel carriers, wherein the metal platinum of the catalyst is in a one-dimensional or two-dimensional highly dispersed state on the surface of the carrier; platinum atoms exist in a single atom or sub-nanometer cluster form; the particle diameter of the sub-nanometer cluster is smaller than 1nm. The invention also discloses a preparation method of the propane dehydrogenation catalyst. Compared with a catalyst prepared by the existing method, the obtained propane dehydrogenation catalyst has the advantages that the conversion rate and the selectivity are obviously improved; the stability is high; good application prospects are realized.

The invention relates to the technical field of rechargeable lithium ion batteries, in particular to a high-performance power battery electrode and a manufacturing method thereof. The manufacturing method is suitable for manufacturing pole pieces of a positive electrode and a negative electrode of a rechargeable lithium ion battery. The manufacturing method comprises the following steps of: coating a conductive layer without lithium storage activity on a metal foil by a water-based process first and then coating a material with the lithium storage activity on the metal foil by using an oil-system formula to obtain a power battery electrode after drying and rolling the conductive layer. The electrode manufacturing method utilizes the advantages of high acting force and low internal resistance of the water-based process and metal, utilizes the characteristics of stable process and long cycle life of the oil-system formula, reduces the using amount of a bonding agent, can greatly improve the high-rate performance and the cycle life of the battery, and is an ideal power battery electrode manufacturing method.

The invention provides a nanocrystalline accumulation meso-microporous ZSM-5 catalyst and preparation and application thereof. The catalyst is aggregated by small grains with particle sizes of 20-100 nm to an aggregation state with a particle size of 200-2000 nm, the aggregation state forms the catalyst, the specific surface area of the catalyst is 350-420 m<2>/g, and the pore volume of the catalyst is 0.25-0.35 cm<3>/g. According to the invention, a mesoporous-microporous composite nanocrystalline accumulation state ZSM-5 molecular sieve is directly synthesized; under the condition of adding no second template, a solid silicon source is pretreated to generate different degrees of depolymerization, the material ratio of the synthesis system is further adjusted, a sodium salt is added to adjust the growth speed in a crystallization process of the molecular sieve, and meanwhile, a two-stage crystallization method is adopted to promote the generation of a crystal nucleus at a low temperature and promote the growth of a crystal at a high temperature, so as to synthesize a serial grain aggregation state ZSM-5 molecular sieve.

A hanger includes a hanger body having a prescribed external peripheral shape on which clothing is hung up. A first magnet is arranged in a projecting manner on a rear side of the hanger body for attaching the hanger to a prescribed suspending place.

A method for fabricating a super-aligned carbon nanotube array includes the following steps: (1) providing a flat and smooth substrate (11); (2) depositing a catalyst layer (12) on the substrate at a rate of less than about 5 nm/s; (3) annealing the catalyst layer at atmosphere; (4) positioning the substrate with the catalyst layer into a furnace; (5) heating the furnace up to a predetermined temperature; and (6) supplying a reaction gas into the furnace, thereby growing a number of carbon nanotubes (22) on the substrate, via the catalyst layer, such that the carbon nanotube array is formed on the substrate.