5328 results about "TO-18" patented technology

Described is a system for wireless energy transfer for person worn peripherals. The system makes use of a technique referred to as strongly-coupled magnetic resonance to transfer energy across a distance without wires and enables efficient transfer of energy over distances of 10 to 18 cm or more. The system comprises a resonant power source, which could be embedded in a person's equipment vest or backpack receiving power from a central battery pack or micro fuel cell, and a resonant power capture unit which could be integrated with the helmet or hand held weapon, electronic device, and the like that may be carried or handled by a person.

The present invention provides probe arrays and methods of using the same for concurrent and discriminable detection of multiple strains of different species. In one aspect, the probe arrays of the present invention are nucleic acid arrays comprising (1) a first group of probes, each of which is specific to a different respective strain of a first species; and (2) a second group of probes, each of which is specific to a different respective strain of a second species. In many embodiments, the nucleic acid arrays of the present invention further include a third group of probes, each of which is specific to a different strain of a third species. In one example, a nucleic acid array of the present invention includes probes for sequences selected from SEQ ID NOs: 1 to 18,598, and can discriminably detect different strains of Streptococcus pyogenes, Streptococcus agalactiae and Staphylococcus epidermidis.

A conjugated polymer has a repeated unit having the structure of formula (I)wherein A1, A2, R1 and R2 are independently selected from the group consisting of a proton, an alkyl group comprising up to 18 carbon atoms, an alkoxy group comprising up to 18 carbon atoms, cyano, nitro, aryls and substituted aryls, and wherein Ar is selected from the group consisting of ethenylene, ethynylene, monocyclic arylene, bicyclic arylene, polycyclic arylene, monocyclic heteroarylene, bicyclic heteroarylene, polycyclic heteroarylene, and one to five such groups one of fused or linked.

A colored film-coated ultraviolet / infrared absorbent glass plate is formed of base glass, colorants, and a colored film. The base glass includes 65 to 80 wt. % SiO2; 0 to 5 wt. % Al2O3; 0 to 10 wt. % MgO; 5 to 15 wt. % CaO; 10 to 18 wt. % Na2O; 0 to 5 wt. % K2O; 5 to 15 wt. % total amount of MgO and CaO; 10 to 20 wt. % total amount of Na2O and K2O; 0.05 to 0.3 wt. % of SO3; and 0 to 5 wt. % B2O3. The colorants includes 0.35 to 0.55 wt. % total iron oxide (T-Fe2O3) expressed as Fe2O3; 0.08 to 0.15 wt. % FeO; 0.8 to 1.5 wt. % CeO2; and 0 to 0.5 wt. % TiO2. FeO expressed as Fe2O3 is equal to or more than 20 wt. % and less than 27 wt. % of T-Fe2O3. The colored film has a red color shade with a thickness between 30 nm and 300 nm and includes fine particles of gold and silicon oxide of more than 50 wt. % and equal to or less than 95 wt. %. The colored film is applied onto a surface of the ultraviolet / infrared absorbent glass plate.

Disclosed and claimed are cocoa extracts, compounds, combinations thereof and compositions containing the same, such as polyphenols or procyanidins, methods for preparing such extracts, compounds and compositions, as well as uses for them, especially a polymeric compound of the formula An, wherein A is a monomer of the formula:wherein n is an integer from 2 to 18, such that there is at least one terminal monomeric unit A, and one or a plurality of additional monomeric units;R is 3-(alpha)-OH, 3-(beta)-OH, 3-(alpha)-O-sugar, or 3-(beta)-O-sugar;bonding between adjacent monomers takes place at positions 4, 6 or 8;a bond of an additional monomeric unit in position 4 has alpha or beta stereochemistry;X, Y and Z are selected from the group consisting of monomeric unit A, hydrogen, and a sugar, with the provisos that as to the at least one terminal monomeric unit, bonding of the additional monomeric unit thereto (the bonding of the additional monomeric unit adjacent to the terminal monomeric unit) is at position 4 and optionally Y=Z=hydrogen;the sugar is optionally substituted with a phenolic moiety, at any position on the sugar, for instance via an ester bond, andpharmaceutically acceptable salts or derivatives thereof (including oxidation products).

Provided is a novel aromatic amine derivative represented by General Formula (G1) below. (In the formula, A represents oxygen or sulfur, and R1 to R7 individually represent any of a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted phenyl group, and a substituted or unsubstituted biphenyl group. In addition, α1 and α2 individually represent a substituted or unsubstituted phenylene group. Further, Ar1 represents a substituted or unsubstituted condensed aromatic hydrocarbon having 14 to 18 carbon atoms included in a ring. Further, Ar2 represents a substituted or unsubstituted aryl group having 6 to 13 carbon atoms included in a ring. Further, j and n are individually 0 or 1, and p is 1 or 2.)

A particulate water absorbing agent of the present invention includes a water absorbent resin, having a cross-linking structure, whose surface has been cross-linked by adding a surface treatment agent, wherein: (i) a mass average particle diameter (D50) ranges from 200 to 600 μm and 95 to 100 wt % of a particulate water absorbing agent whose particle diameter ranges from less than 850 μm to not less than 150 μm is contained with respect to 100 wt % of whole the particulate water absorbing agent, and (ii) a logarithmic standard deviation (σζ) of particle size distribution ranges from 0.25 to 0.45, and (iii) a compressibility rate defined by a following equation ranges from 0 to 18%, and (iv) a surface tension of a supernatant liquid obtained in 4 minutes after dispersing 0.5 g of the particulate water absorbing agent in 50 ml of physiological saline whose temperature is 20° C. is 55 mN / m or more, the compressibility rate (%)=(P−A) / P×100 where P represents a tapped bulk density of the particulate water absorbing agent and A represents a loose bulk density of the particulate water absorbing agent.

Disclosed are a low-dielectric-constant glass fiber having a glass composition comprising, by weight %, 50 to 60% of SiO2, 10 to 18% of Al2O3, 14% to less than 20% of B2O3, 1% to less than 6% of MgO, 2 to 5% of CaO, 0.5 to 5% of TiO2, 0 to 0.3% of Li2O, 0 to 0.3% of Na2O, 0 to 0.5% of K2O and 0 to 2% of F2, the content of MgO+CaO being 4 to 11% and the content of Li2O+Na2O+K2O being 0 to 0.6%, and a glass fiber fabric made of the low-dielectric-constant glass fiber. The glass fiber of the present invention has a low dielectric constant and a low dielectric tangent, is excellent in productivity and workability and is also excellent in water resistance, and the glass fiber is suitable for reinforcing printed wiring boards for high-density circuits.

Provided are a glass sheet for a CIGS solar cell which satisfies both of high power generation efficiency and high glass transition temperature, and a CIGS solar cell having high power generation efficiency. A glass sheet for a Cu—In—Ga—Se solar cell containing, in terms of mol % on the basis of the following oxides, 60 to 75% of SiO2, 3 to 10% of Al2O3, 0 to 3% of B2O3, 5 to 18% of MgO, 0 to 5% of CaO, 4 to 18.5% of Na2O, 0 to 17% of K2O, and 0% or more and less than 10% of SrO+BaO+ZrO2, wherein K2O / (Na2O+K2O) is 0 to 0.5, and the glass sheet has a glass transition temperature (Tg) of more than 550° C.

A glass substrate of the present invention for magnetic recording media having high heat resistance and easy chemical strengthening ability at once has not been obtained, which is a glass composition essentially comprising 60 to 70 wt % SiO2, 5 to 20 wt % Al2O3, 0 to 1 wt % Li2O, 3 to 18 wt % Na2O, 0 to 9 wt % K2O, 0 to 10 wt % MgO, 1 to 15 wt % CaO, 0 to 4.5 wt % SrO, 0 to 1 wt % BaO, 0 to 1 wt % TiO2 and 0 to 1 wt % ZrO2, wherein the sum of Li2O, Na2O and K2O is from 5 to 25 wt %, and the sum of MgO, CaO, SrO and BaO is from 5 to 20 wt %.

A home security system which includes sensors 11 to 18 that detect an alarming situation in different locations inside a facility, cameras 21 to 26 that capture images of different locations inside a facility, and a controller 30 that memorizes the associations between sensors 11 to 18 and cameras 21 to 26, and when any of the sensors 11 to 18 detects an alarming situation, has cameras that are associated with the sensors that have detected an alarming situation capture images based on the associations, and also updates the memorized associations.

A home security system which includes sensors 11 to 18 that detect an alarming situation in different locations inside a facility, cameras 21 to 26 that capture images of different locations inside a facility, and a controller 30 that memorizes the associations between sensors 11 to 18 and cameras 21 to 26, and when any of the sensors 11 to 18 detects an alarming situation, has cameras that are associated with the sensors that have detected an alarming situation capture images based on the associations, and also updates the memorized associations.

The present invention provides a fruiter cut concrescence protectant, belonging to foliage cut concrescence protectant technology field, the aim is to solve the problem of the existing technology that fruiter cut concrescence is slow, it is easy to be damaged by insect so as to affect fruiter growth. The protectant of the present invention comprises: forming-film bond, nutrition agent, regulator, insecticide, antiseptic and booster, their weight mixing ratio is 10 to 20 shares, 2 to 20 shares, 0.1 to 1.0 share, 5 to 18 shares, 5 to 16 shares, 1 to 10 shares separately. The fruiter cut cicatrizes rapidly, effect is excellent, pest control capacity is strong, the protectant is suitable for fruit tree such as Chinese date, apply and pear as well as the cut concrescence of pruning cut, annulus peelling cut, engraft cut, saw cut, touching injure as well as damnification surface etc.

The invention provides a high-temperature resistant environment-friendly polyvinyl chloride material for wires and cables. A raw material formulation mainly comprises the following materials in weight portion: 80 to 120 portions of loose-type polyvinyl chloride resin, 20 to 55 portions of tetraoctyl pyromellitate, 5 to 35 portions of polyester plasticizer and 12 to 18 portions of calcium-zinc stabilizer, wherein the polymerization degree of the loose-type polyvinyl chloride resin is between 2,000 and 3,000; in the calcium-zinc stabilizer, the total content of lead, cadmium, mercury and hexavalent chromium is less than or equal to 10 ppm of the total weight of the calcium-zinc stabilizer; the polyester plasticizer is polypropylene-1, 2-glycol adipate or polypropylene-1, 3-butylene terephthalate; and the molecular weight of the polyester plasticizer is between 3,000 and 4,000. After the material is aged in a hot-air oven for 168 hours at 158 DEG C, the retention rate of tensile strength is up to 106 percent; the retention rate of elongation at break is 97 percent; and the material is good in mechanical physical properties and insulating property. Therefore, the material meets the temperature-resistant requirement on long-term operating temperature at 125 DEG C in UL1581.

The invention discloses polymer electrolyte for a lithium ion battery and a manufacturing method of a battery thereof. The electrolyte is formed by dissolving 0.5 to 15 percent of electrochemical inert polymer with the molecular weight of 5000 to 120000, 6 to 18 percent of lithium salt and various functional additives into a non-aqueous solvent. The additives comprise a film forming additive, an overcharging prevention additive, a flame-retardant additive, a lithium salt stabilizer and a surfactant for enhancing the soaking performance of the electrolyte. In order to solve the preparation difficulty and the performance defect of a polymer battery at present, the invention selects a polymer with proper molecular weight and other functional components of the electrolyte creatively. By the electrolyte, the battery can have the characteristics of a traditional polymer battery and a traditional liquid-state battery, the safety performance, the service life, the high / low-temperature performance and the magnification performance of the battery are comprehensively enhanced, and the preparation of the battery is simple and easy.

An ozone generator which operates at constant pressures to produce a continuous flow of ozone in an oxygen stream having from 10% to 18% by weight of ozone. The ozone generator includes one or more electrolytic cells comprising an anode / anode flowfield, a cathode / cathode flowfield, and a proton exchange medium for maintaining the separation of ozone and oxygen from hydrogen. The ozone generator also has an anode reservoir which vents oxygen and ozone and a cathode reservoir which vents hydrogen. The anode reservoir can be filled from the cathode reservoir while continuing to produce ozone. The ozone generator is readily configured for self-control using a system controller programmed to operate the anode reservoir at a constant pressure.

The present invention relates to polyglycerol partial esers of polyhydroxystearic acid and polyfunctional carboxylic acids which are obtainable by esterification of a polyglycerol mixture with polyhydroxystearic acid where N=1 to 10, preferably 2 to 8, in particular 3 to 5 units and dimer fatty acids which have been obtained by catalytic dimerization of unsaturated fatty acids having 12 to 22 C atoms and have an average functionality of 2 to 3, and / or with aliphatic, linear or branched dicarboxylic acids having a chain length of 2 to 16 C atoms and additionally saturated or unsaturated, linear or branched fatty acids having 6 to 22 C atoms, preferably 12 to 18 C atoms, the degree of esterification of the polyglycerol mixture being between 20 and 75%, preferably 40 to 70%.

The invention discloses low-yield ratio and high-strength steel for bridges and a manufacturing method thereof. The steel comprises the following chemical components by weight percent : 0.06-0.10 percent of C, 0.20-0.45 percent of Si, 1.20-1.50 percent of Mn, no more than 0.010 percent of P, no more than 0.0020 percent of S, 0.30-.060 percent of Ni, 0.20-0.50 percent of Cu, 0.15-0.50 percent of Mo, 0.025-0.060 percent of Nb, no more than 0.035 percent of Ti, 0.020-0.040 percent of Alt, and Fe and unavoidable impurities in balancing amount. According to the invention, through smelting, refining, performing a reasonable thermo-mechanical control process (TMCP) and optimizing tempering heat treatment production, the tensile strength of the steel is 700-780 MPa, the yield strength is 530-600MPa, the extensibility is greater than or equal to 18 percent, the yield ratio is less than or equal to 0.80, and 40 below zero DEG C low-temperature longitudinal impact is greater than or equal to 100 J, so that the steel is good in obdurability matching and low in the yield ratio, is provided with excellent performance of shock prevention, and is stable in production process and strong in operability.

Disclosed is an abrasive tool made of epoxy resin-bonded compound abrasive material, which comprises epoxy resin, abrasive material and curing agent. The weight percentages are as follow: the epoxy resin is 15 to 78 percent, the abrasive material is 2 to 44 percent and the curing agent is 4 to 18 percent. Wherein, the abrasive material comprises one of diamond, silicon carbide or corundum or the combination of more than one material. The curing agent comprises one of 4.4`-methylenedianil, solid diaminodiphenyl methane or liquid modified diaminodiphenyl methane or the combination of more than one material. The component of the abrasive tool also comprises the other auxiliary material, which comprises one of alumina, barium chloride, sodium chloride, quartz sand, organobentonite, wetting agent, zirconium silicate, calcium carbonate, graphite powder, garnet, magnesium sulfate, phenolic resin, zinc stearate and magnesium stearate, or the combination of more than one material. The product can be made into any shape the same with the present product, which can be applied in various grinding and polishing equipment with wide application scope.

The invention discloses bio-organic fertilizer, and belongs to the technical field of organic fertilizer. The proportion by weight of all raw materials of the bio-organic fertilizer is dried chicken manure : edible mushroom : compound microbial agent : corn flour or rice bran : functional strain = 110-140 : 390-360 : 0.1-0.5 ; 0.1. The compound microbial agent comprises mould, bacillus, lactic acid bacteria, actinomycetes and saccharomycetes. The strains are efficient viable bacteria. Each gram of the compound microbial agent comprises the number of the mould ranges from 5 hundred million to 8 hundred million, the number of the efficient viable bacteria of bacillus ranges from 12 hundred million to 15 hundred million, and the number of the actinomycetes ranges from 10 hundred million to 12 hundred million and the saccharomycetes of 15 hundred million to 18 million. According to the bio-organic fertilizer, the chicken manure and mushroom dregs serve as main materials, and the high-quality organic fertilizer can be fermented quickly by adding the compound microbial agent and the functional strain.

A polyoxyalkylene derivative is represented by formula (I): wherein Z represents a residue of a compound having 2 to 8 hydroxyl groups; AO represents an oxyalkylene group having 2 to 18 carbon atoms; n and m each represent an integer of 0 to 2000 provided that both n and m do not represent 0; a and b each represent an integer satisfying the relationships: 2≦a+b≦8 and 1≦b; R represents a hydrocarbon group having 1 to 30 carbon atoms; and X represents a divalent hydrocarbon group having 3 to 10 carbon atoms.

An optical glass having a high light transmittance, a high refractive index and excellent production stability, which contains at least one of CaO and SrO together with SiO2, B2O3, La2O3, Nb2O5, TiO2 and BaO, having a composition that substantially contains, by weight %, 1 to 18% of SiO2, 3 to 24% of B2O3, provided that the ratio of content of B2O3 to the content of SiO2 (B2O3 / SiO2) is over 1, 10 to 50% of La2O3, 1 to 30% of Nb2O5, 1 to 30% of TiO2, over 6% but not more than 25% of BaO, less than 7% of CaO, 6% or less of SrO, 0 to 13% of MgO, provided that the total content of BaO, CaO, SrO and MgO is 40% or less, 0 to 15% of ZnO, 0 to 15% of ZrO2, 0 to 10% of Al2O3, 0 to 20% of Gd2O3, 0% or more but less than 2% of Y2O3, 0 to 5% of Yb2O3, 0 to 18% of Ta2O5, 0 to 20% of Bi2O3, 0 to 10% of GeO2, 0% or more but less than 2% of Sb2O3, and 0% or more but less than 2% of SnO2, and having a refractive index (nd) of over 1.8, Abbe's number (νd) of 28 to 40 and a density of 4.2 g / cm3 or more.

The invention discloses a composite phase-change energy storage material for microcapsules and a preparation method thereof. The coating of the microcapsule is made of silicon dioxide, and the core of the microcapsule is made of a phase-change energy storage material, wherein the phase-change energy storage material is a paraffin organic solid-liquid phase-change energy storage material. 0.2 to 0.5 wt.% of dispersed emulsifier, 52.5 to 62.5 wt.% of solvent water, 18.75 to 31.5 wt.% of phase-change energy storage material and 15.5 to 18.75 wt.% of inorganic silica source are matched and put into a reactor for stirring for 5 to 8 hours; the mixture is uniformly dispersed and emulsified at the temperature 3 to 8 DEG C higher than that for solid-liquid phase change; hydrochloric acid aqueous solution catalyst with the pH value of 0.93 to 4.07 or sodium hydroxide aqueous solution catalyst with the pH value of 8.0 to 12.0 is added into the emulsion; the reacting solution is naturally cooled to room temperature and precipitation solution is obtained; the precipitate is washed with the combination of water and petroleum ether, wherein the mass percent of the petroleum ether is 30 wt.%; then the precipitate is washed with deionized water and is filtered, and the product is naturally aired. The invention improves the technology of phase-change energy storage and conservation, and has the function of automatic temperature regulation, favorable physical and chemical stability, crack resistance, flame retardancy, wear resistance and high thermal conductivity.

The invention belongs to the technical field of lithium ion batteries, and particularly relates to a composite porous diaphragm which comprises an organic layer and an inorganic coating arranged on the surface of the organic layer, wherein the organic layer is a polyolefin porous diaphragm layer; the inorganic coating comprises the following components in percentage by weight: 0.2-2% of water-soluble high molecular thickener, 0.2-5% of waterborne dispersing agent, 1-30% of waterborne latex and 63-98.6% of inorganic particles; and the waterborne latex is a high-molecular polymer of which the solubility parameter is less than or equal to 18(J / cm<3>)1 / 2 and the surface tension is less than or equal to 44 dynes / cm. Compared with the prior art, the composite porous diaphragm provided by the invention has good heat-resistant shrinkage performance; and meanwhile, with better puncture strength, the inorganic coating of the diaphragm effectively reduces the short-circuit risk in a battery, and improves the safety performance of the battery. Moreover, the invention also discloses a preparation method of the diaphragm.

The invention relates to an aqueous inorganic zinc-enriched coating and a preparation method thereof. The coating is prepared by mixing a component A and a component B in a weight ratio of 1: 1.5-3.5. The preparation method for the component A comprises the following steps of: mixing 45 to 70 weight parts of alkaline metal silicate solution, 0 to 8 weight parts of water-soluble resin, 0.1 to 15 weight parts of modifying agent with stirring at an intermediate speed; and then adding 10 to 35 weight parts of deionization water, 2 to 18 weight parts of inorganic filling, 1 to 10 weight parts of crystal whisker reinforced material, 0.5 to 3.5 weight parts of aqueous auxiliary agent which comprises a dispersant, a thickening agent and a foam suppressor, and mixing the mixture to obtain the component A. The component B is prepared by the following steps of: mixing 95 to 98 weight parts of spherical zinc powder and 2 to 5 weight parts of curing agent. The coating prepared by the method has good early waterproof resistance, good flexibility, good impact resistance, strong construction adaptability and good salt mist corrosion resistance.

A thermal transfer printing medium that contains a thermal transfer layer which contains a first taggant and colorant, wherein: the first taggant comprises a fluorescent compound with an excitation wavelength selected from the group consisting of wavelengths of less than 400 nanometers, wavelengths of greater than 700 nanometers. When the thermal transfer layer is printed onto a white polyester substrate with a gloss of at least about 84, a surface smoothness Rz value of 1.2, and a reflective color represented by a chromaticity (a) of 1.91 and (b) of −6.79 and a lightness (L) of 95.63, when expressed by the CIE Lab color coordinate system, and when such printing utilizes a printing speed of 2.5 centimeters per second and a printing energy of 3.2 joules per square centimeter, a printed substrate with certain properties is produced. The printed substrate has a reflective color represented by a chromaticity (a) of from −15 to 15 and (b) from −18 to 18, and the printed substrate has a lightness (L) of less than about 35, when expressed by the CIE Lab color coordinate system. When the printed substrate is illuminated with light source that excites the first taggant with an excitation wavelength selected from the group consisting of wavelengths of less than 400 nanometers, wavelengths greater than 700 nanometers, the printed substrate produces a light fluorescence with a wavelength of from about 300 to about 700 nanometers.

The invention relates to non-water electrolyte for a high-voltage lithium ion battery and a preparation method. The non-water electrolyte is characterized in that: respectively purifying sulphone compound, halogenated cyclic carbonic ester and carbonic ester through rectification and molecular sieving under the protection of argon or nitrogen; mixing the sulphone compound, the halogenated cyclic carbonic ester and the carbonic ester in the weight ratio of 1:1:2 to obtain a non-water mixed solvent from which impurities and water are removed; dissolving 10 to 18 percent of mixed lithium salt in 80 to 87 percent of non-water mixed solvent to obtain the electrolyte; adding 2 to 5 percent of additive into the electrolyte; and uniformly mixing at the temperature of 40 DEG C to obtain the non-water electrolyte for a 4.8 Vvs.Li+ / Li lithium ion battery. The electrolyte has higher compatibility with a cathode material under high voltage and can form a stable solid electrolyte interface (SEI) film on the surfaces of a positive electrode and a negative electrode. Besides, the invention has the advantages that: the preparation process is simple, and the method is easy to implement and suitable for industrialized production.

Disclosed herein is a thermoplastic composition comprising a combination of: a polysiloxane-polycarbonate copolymer and a poly(aliphatic ester)-polycarbonate copolymer comprising soft block ester units of the formula (8a):wherein m is 4 to 18, wherein the thermoplastic composition has a melt volume rate of 14 cc / 10 min to 22 cc / 10 min at 300° C. and under a load of 1.2 Kg and a dwell time of 6 minutes, according to ASTM D1238-04, wherein an article molded from the thermoplastic composition and having a thickness of 3.2 mm has a percent transmittance of greater than 85% according to ASTM D1003-00, and wherein 100% of a set of five test articles each having a thickness of 3.2 mm and molded from the thermoplastic composition exhibit ductile fracture at −40° C. when measured for notched Izod Impact according to ASTM D256-04. An article comprising the thermoplastic composition is also disclosed.