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142results about How to "Small hindrance" patented technology

Heat-Generating Element for an Electric Heating Device and Method for the Manufacture of the Same

ActiveUS20080099464A1Compensation of toleranceUse economicallyHeater elementsAir heatersStructural unitElectric heating
A heat-generating element includes at least one PTC heating element, strip conductors lying flat on it on both sides, and a frame which forms at least one frame opening for holding the at least one PTC heating element. The frame, as a part of a housing, forms a structural unit with a wedge element having a first wedge surface that extends parallel to the strip conductor and a second wedge surface that lies exposed on the exterior side of the housing and that is aligned diagonally to the first wedge surface. For fixing the heat-generating element precisely in place in a slot in the housing, the heat-generating element has spacing surfaces positioned upstream or downstream of the at least one PTC heating element in the direction of the length of the slot. Also provided is a method of manufacturing an electric heating device.
Owner:CATEM

Refrigeration cabinet

A refrigeration cabinet, in particular a commercial refrigerator or freezer, is provided. The refrigeration cabinet has a housing, which has a front access opening, a door, which has at least one door leaf, for the access opening, and a guide. The door leaf has a height and a width and is mounted such that it can be rotated about a vertical rotation axis and can be displaced transverse to the rotation axis. The guide defines a movement of the door leaf between a closed position and an open position in such a way that the pivot region of the door leaf projects less than a full door-leaf width into the exterior in front of the access opening, and that the door leaf is mounted such that it can be rotated about a vertical axis and can be displaced transverse to the rotation axis.
Owner:SCHOTT AG

Excellent boiling-resistant and neutral-salt-mist-resistant polyester resin for low-temperature curing type powder and preparation method thereof

The invention belongs to the technical field of resin for coatings, particularly relates to excellent boiling-resistant and neutral-salt-mist-resistant polyester resin for a TGIC system low-temperature curing type powder coating, and further relates to a preparation method of the polyester resin. The excellent boiling-resistant and neutral-salt-mist-resistant polyester resin for the TGIC system low-temperature curing type powder coating is mainly prepared from the following raw materials in parts by mole through a polymerization reaction: 8-20 parts of terephthalic acid, 12-25 parts of dodecenyl succinic anhydride, 6-15 parts of isophthalic acid, 12-28 parts of 1H, 1H, 12H, 12H-perfluoro-1,12- dodecanediol, 7-18 parts of neopentyl glycol, 8-20 parts of 2, 2, 3, 3-tetrafluoro-1, 4-butanediol and 5-10 parts of 2, 2-difluoromalonic acid. The TGIC system powder coating finally prepared by the product disclosed by the invention can realize 150 DEG C / 15min low-temperature curing film formation, the coating quality meets the requirements of a powder coating film, and the coating film has outstanding boiling resistance and neutral salt mist resistance.
Owner:HUANGSHAN HUIZHOU KANGJIA CHEM CO LTD

Ultrafast-response overcharge-prevention electrochromic device and preparation method thereof

The invention discloses an ultrafast-response overcharge-prevention electrochromic device and a preparation method thereof. The ultrafast-response overcharge-prevention electrochromic device comprisesa first transparent electrode, an ionic conduction layer, an organic electrochromic layer, an inorganic electrochromic layer and a second transparent electrode which are arranged in a sequentially laminated way. The ultrafast-response overcharge-prevention electrochromic device has the following beneficial effects that (1) the ionic conduction layer has the great pore diameter and is provided with many pore passages and facilitates positive ion transmission, so that the response speed of the device is accelerated; (2) the cooperative action of a plurality of positive ions is realized in the electrochromic process of the electrochromic device, so that the device has very high regulation capability; (3) in the ultrafast-response overcharge-prevention electrochromic device, a resin layer perse has good insulation capability, so that the electricity leakage can be prevented without adding an electron blocking layer; and (4) the wetting performance of a solid-liquid interface is better than that of solid-solid interface contact, so that the steric hindrance between interfaces is reduced, and the very high coloring efficiency is realized.
Owner:SHANGHAI INST OF CERAMIC CHEM & TECH CHINESE ACAD OF SCI

Method for directly separating CD<4+> and CD<8+> lymphocytes

The invention discloses a method for directly separating CD<4+> and CD<8+> lymphocytes, lays a better foundation for the subsequent research on the CD<4+> and CD<8+> lymphocytes, and relates to the field of biomedicines. The method comprises steps of: multi-arm well and star-shaped polymer and mouse anti-human CD<4+> or CD<8+> monoclonal antibody covalent coupling, long-chain biotin molecule coating through utilizing a mouse anti-human CD<4+> or CD<8+> monoclonal antibody-modified multi-arm well and star-shaped polymer, peripheral blood sample CD<4+> and CD<8+> lymphocyte acquiring through utilizing a mouse anti-human CD<4+> or CD<8+> monoclonal antibody and long-chain biotin co-modified multi-arm well and star-shaped polymer, peripheral blood long-chain biotinylation multi-arm well and star-shaped polymer identifying and coupling through utilizing streptavidin-modified nano magnetic beads, captured CD<4+> and CD<8+> lymphocyte separating and suspending and the like. A suspension can be directly used for subsequent analysis; and compared with a conventional cell separating method, the method is suitable for magnetically separating complicated peripheral blood sample CD<4+> and CD<8+> lymphocytes, so that the peripheral blood sample CD<4+> and CD<8+> lymphocyte separation efficiency is increased.
Owner:NANCHANG UNIV

Schizophyllan modified sodium hyaluronate microsphere gel, preparation method of sodium hyaluronate microsphere gel, and application of sodium hyaluronate microsphere gel in cosmetics

The invention provides schizophyllan modified sodium hyaluronate microsphere gel, a preparation method of the sodium hyaluronate microsphere gel, and application of the sodium hyaluronate microspheregel in cosmetics. The method comprises the following steps: adding dried sodium hyaluronate powder into a hyaluronidase solution, and performing enzymolysis to obtain a sodium hyaluronate small-molecule solution; slowly adding the sodium hyaluronate small-molecule solution into a mixed oil phase, slowly stirring, adding a mixed cross-linking agent of calcium chloride and divinyl sulfone, cross-linking and curing to obtain sodium hyaluronate microspheres; adding the sodium hyaluronate microspheres and pre-treated schizophyllan into an alkaline solution containing polyethylene glycol, uniformlystirring, regulating the pH value of the system to be neutral, adding a phosphate buffer solution, standing and aging, thereby obtaining the schizophyllan modified sodium hyaluronate microsphere gel.The schizophyllan modified sodium hyaluronate microsphere gel prepared by the method disclosed by the invention is small in particle size, easily penetrates into the deep part of skin, can form tiny gel with protein-water, achieves the effect of deeply moisturizing for a long time, and has excellent moisture retention property.
Owner:DONGGUAN LIANZHOU INTPROP OPERATION MANAGEMENT CO LTD

Escherichia coli detection method based on time-resolved fluorescence method and DNA hybridization

The invention discloses an escherichia coli detection method based on a time-resolved fluorescence method and DNA hybridization. A capture probe DNA1 and an identifying probe DNA 2 are designed according to a DNA target sequence of escherichia coli; the capture probe DNA1 is fixedly marked on a glass sheet; and the identifying probe DNA 2 is jointed with long-life luminescent rare-earth europium complex. When the capture probe DNA1 and the identifying probe DNA 2 are connected in series and can generate base-pair complementary hybridization reaction with the target DNA (DNA of biology to be detected); and a DNA detection model based on two serial-connected probes on the surface of the glass sheet is established. The long-life luminescent rare-earth europium complex is used as a marker distinguishing the probe DNA 2; and the time-resolved fluorescence method can effectively eliminate the disturbance of fluorescent sources in a biological system and background light of a solid matrix. The detection method takes little time, is visual, flexible, accurate in reaction results and has very obvious advantages.
Owner:HUNAN UNIV
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