37results about How to "Reduce reversibility" patented technology

A positive active material for lithium secondary batteries, includes a composite oxide including an oxide which is represented by the composite formula Li_xMn_aNi_bCo_cO₂ and has an α-NaFeO₂ structure, and an impurity phase including Li₂MnO₃. The values a, b, and c are within such a range that in a ternary phase diagram showing the relationship among these, (a, b, c) is present on the perimeter of or inside the quadrilateral ABCD defined by point A (0.5, 0.5, 0), point B (0.55, 0.45, 0), point C (0.55, 0.15, 0.30), and point D (0.15, 0.15, 0.7) as vertexes, and 0.95<x/(a+b+c)<1.35.

A shear strain type pressure sensor comprises a shell. A magnetic field generating device in the shell comprises two magnetic poles which are opposite in magnetism and correspond to each other oppositely. A shear plate is arranged in the gap between the two magnetic poles, a rubber sheet is fixed on one side of the shear plate and in full contact with the end face of the first magnetic pole in the two magnetic poles, and a first electrode is fixed on the other side of the shear plate and fixedly provided with a magnetorheological elastomer. A second electrode is fixed on the other side of the magnetorheological elastomer, the second electrode is fixedly connected with the end face of the second magnetic pole in the two magnetic poles, the first electrode and the second electrode are electrically connected with a signal conditioning module, one end of the shear plate upwards extends to penetrate through an S-shaped force measuring piece and then extends out of the upper end face of the shell, a supporting plate used for supporting the S-shaped force measuring piece is fixed in the shell, a stop piece is arranged on the shear plate, and the lower end face of the stop piece is in contact with the upper end face of the S-shaped force measuring piece. The shear strain type pressure sensor is high in resolution, high in sensitivity, and large in force testing range.

A novel hydrogel delivery systems useful for encapsulating and releasing pharmaceuticals or chemicals is disclosed where water soluble polymers containing crosslinker repeating units that associate or dissociate with complementary crosslinking repeating units or separate linkers to reversibly crosslink the hydrogel. In an exemplary embodiment, a DNA crosslinked hydrogel displays photoreversibility. An exemplary hydrogel delivery system comprises DNA polymer conjugates, wherein complementary DNA sequences are crosslinked with polymer chains and hybridization of the DNA sequences is controlled by photoresponsive moieties. Such hydrogels can be used to release drug molecules and/or other therapeutic reagents. The exemplary hydrogel employs photosensitive azobenzene moieties that are incorporated into the DNA crosslinker units. The azobenzene moieties respond to different wavelengths of light so that the state of azobenzene isomerization is induced by the proportion of visible and UV light irradiated. The isomer state of the azobenzene dictates whether the complementary DNA sequences hybridize to cross link the DNA polymer conjugates. Thus, irradiation of light (visible or UV) can transform the hydrogel network between a sol and any of multiple gel states to regulate the degree of crosslinking between complementary DNA sequences and, therefore, provide a profile of release of a hydrogel encapsulated pharmaceutical or other chemical.

An anode material for use in a metal secondary battery contains MgH₂, and a metal catalyst which is in contact with the MgH₂ and improves the reversibility of a conversion reaction. The metal secondary battery includes a cathode active material layer, an anode active material layer, and an electrolyte layer that is formed between the cathode active material layer and the anode active material layer, and the anode active material layer contains the anode material. A method for the production of an anode material for use in a metal secondary battery includes a contacting step of contacting MgH₂ with a metal catalyst which improves the reversibility of a conversion reaction.

The invention relates to the technical field of fluorine chemical engineering, in particular to an application method for preparing an electronic grade hydrogen fluoride process device. The method ischaracterized in that high-boiling residues HAsF6 and MAsF6 are produced through arsenic impurity in fluorine oxidized hydrogen fluoride, and the pure electronic grade hydrogen fluoride is separated from a multi-component composition through volatility difference of the high-boiling residues HAsF6 and MAsF6, HF and other components and multiple equilibrium processes. A rectification technical process adopts reflux liquid and upward gas to form gas and liquid countercurrent contact in a distillation tower, volatile component products with high purity can be obtained from the top of the tower, and non-volatile component products with high purity can be obtained from the bottom of the tower. The main component of tail gas produced from hydrogen fluoride rectification mainly comprises HF steam, the tail gas further comprises the following volatile components: SO2, SiF4, PF3, POF3, AsF5, SF6 and PF5, and the tail gas can be completely washed with pure water, condensed and recycled to prepare technical grade hydrofluoric acid.

The invention discloses a multi-column strip-shaped packaging machine, which comprises a rack, and a paper supporting part, a filling and metering device, a bag forming mechanism, a middle sealing device, a horizontal sealing device, a cutter device, a bag turnover mechanism and a sliding chute arranged on the rack. The cutter device comprises cutter support plates, two cutter shafts, cutters, support rods and bag guiding supports; the two cutter shafts are arranged on the cutter support plates at an interval; the cutters are arranged on the cutter shafts; the two cutter shafts are connected with air cylinders; the support rods are arranged between the two cutter support plates, and are located above the cutters; the bag guiding supports are arranged on the support rods; and loaded packaging bags are cut by the cutters after passing through the bag guiding supports. According to the multi-column strip-shaped packaging machine provided by the invention, the loaded packaging bags are limited through the bag guiding supports and can be smoothly fed into a position between the cutters so as to be cut.

The present invention relates to a method for increasing the binding reversibility of a ω-conotoxin to a N-type calcium channel, which comprises preparing a ω-conotoxin having a Ile and/or Ala residue at a position of amino acid (11 and/or 12), respectively in the second loop between cysteine residues (2 and 3) of the ω-conotoxin represented by the formula I, such that the prepared ω-conotoxin has the increased binding reversibility to N-type calcium channel. In addition, the present invention relates to a novel ω-conotoxin and a pharmaceutical composition having plausible properties in view of blocking activity to and specificity to N-type calcium channel, and dramatically improved binding reversibility to N-type calcium channel.

The invention discloses a triangular paper folding device and method for paper jams and an automatic regulating mechanism. The automatic regulating mechanism comprises a conveyor belt, the triangular paper folding device, a mounting plate, a transmission component, a first drive device and a second drive device, wherein one end of the mounting plate is connected with the triangular paper folding device, and the other end of the mounting plate is connected with the transmission component; the transmission component is connected with the first drive device and the second drive device. The triangular paper folding device comprises a triangular paper folding block, a horizontal paper folding assembly and an oblique paper folding assembly, wherein the surface, needing to be turned over, of paper is turned over by 90 degrees through the triangular paper folding block, the paper continues to be turned over by 90 degrees by the horizontal paper folding assembly and the oblique paper folding assembly, and then paper folding is completed. The first drive device is used for regulating the horizontal position of the triangular paper folding device, and the second drive device is used for regulating the vertical position of the triangular paper folding device. The triangular paper folding device is simple in structure, low in cost, convenient and reliable to regulate and high in degree of automation, and improves the paper folding precision.

The invention relates to the technical field of fluorine chemicals and in particular relates to electron-grade hydrogen fluoride preparation procedures which are characterized by comprising an evaporation circulation oxidation reaction procedure, a circulating fluidized bed distillation procedure and a washing, absorption and condensation procedure.

The invention belongs to the technical field of fluorine chemistry, and more specifically relates to an electronic grade hydrogen fluoride preparation device. The electronic grade hydrogen fluoride preparation device comprises a transpiration circulation reactor, a circulating fluidized bed distillation column, and a washing absorption condensing tower assembly.

The present invention provides a rechargeable battery including an electrolyte, a positive electrode, a negative electrode, an isolation membrane arranged between the positive electrode and the negative electrode, an active substance of said positive electrode including one or more of manganese oxide and manganese oxyhydroxide an active substance of said negative electrode including zinc and electrolyte salts in said electrolyte contain one or more of zinc alkylsulfonate, zinc arylsulfonate, zinc fluoroborate, zinc alkylsulfate hydrate, zinc arylsulfonate hydrate and zinc fluoroborate hydrate. The rechargeable battery, according to the present invention, will not only effectively avoid the irreversible sulfation of the positive electrode, improve the reversibility of the positive electrode, significantly prolong the cycle life of the rechargeable battery and achieve a higher energy density as well, but also avert problems of chloride ions corrosion and frequent nitrate ions reduction. Compared with the lithium battery on the market, the rechargeable battery according to the present invention uses low-cost materials, and therefore has better economic benefits.