327results about How to "Improve charge acceptance" patented technology

This invention relates to the plus plate lead paste of lead-acid battery comprising (by weight percentages based on lead powder): lead powder 100%, 1.4g/cm3 sulfuric acid 8-12%, deionized water 9-11%, lead dioxide 3-4.2%, short fiber 0.05-0.06%, carbon fiber 0.10-0.15%, anisotropic graphite 0.2-0.4% and bismuth oxide 0.05-0.11%. In this invention, on the based on certain water and acid content in the active substance, additional positive pole active substances are added such as anisotropic graphite and bismuth oxide or the like. The changed components improve the primary battery volume and the ratio of weight/energy with prolonging battery service life.

The invention provides a variable-polarity lead-acid battery and a using method of the variable-polarity lead-acid battery. Positive and negative plates of the lead-acid battery consist of the same grids and lead plasters, and after one or more times of charge-discharge cycle of the battery, the polarities of the positive and negative plates are exchanged. The variable-polarity lead-acid battery has the advantages that the problem of vitriolization of an ordinary lead-acid battery can be solved, the service life of the battery is prolonged, and the utilization ratio of active substances is increased at the same time, so that the charge receptivity and the discharge capacity of the battery are greatly improved.

The invention relates to a lead plaster for a low temperature resistant lead storage battery for an electric scooter and a preparation method of the lead plaster. The lead plaster comprises an anode lead plaster and a cathode lead plaster, wherein the anode lead plaster comprises the following components in parts by weight: 950-970 parts of lead powder, 80-86 parts of 1.3-1.4g/cm<3> sulfuric acid, 110-125 parts of pure water, 3.0-4.0 parts of colloidal graphite, 30-50 parts of red lead, 1.0-1.5 parts of tin sulfate, 0.5-1.0 part of sodium sulfate and 0.7-0.9 part of short fiber; the cathode lead plaster comprises the following components in parts by weight: 1000 parts of lead powder, 75-81 parts of 1.3-1.4g/cm<3> sulfuric acid, 105-120 parts of pure water, 0.6-0.8 part of short fiber, 6.0-7.0 parts of barium sulfate, 1.0-1.5 parts of Norway lignin, 4.0-5.0 parts of humic acid, 3.0-5.0 parts of acetylene black and 1.0-1.5 parts of semi-carbonized saw dust. According to the lead plaster and the preparation method thereof, the acceptance performance when the battery is charged at low temperature is improved and the discharge capacity is increased; the lead plaster disclosed by the invention is applicable to low-temperature environment and is especially suitable for northeast and northwest regions in China.

The invention provides a lead-acid storage battery negative lead plaster capable of inhibiting hydrogen evolution and a preparation method. The technical scheme of the lead-acid storage battery negative lead plaster is as follows: the lead plaster is prepared from the following solid raw materials in parts by weight: 100 parts of lead powder, 1-3 parts of carbon source, 0.15-1.0 part of zinc source, 0.3-2 parts of barium sulfate, 0.1-0.5 part of sodium lignosulfonate and 0.01-0.5 part of fibers. The lead-acid storage battery negative lead plaster provided by the invention is characterized in that a certain quantity of zinc-containing compounds and different types of carbon are added to the negative lead plaster, so that the grain size and the microstructure of the lead negative material are improved, and therefore, the purposes of increasing the capacity of a lead-acid battery, enhancing the ability of the battery to accept charging and improving the charge-discharge cycle stability of the battery are achieved. Tests indicate that the doping of the zinc compound in the negative lead plaster causes the hydrogen evolution potential at the cathode of a lead-acid storage battery to be more negative, so that the hydrogen evolution difficulty is increased, the hydrogen evoluted is reduced, the consumption amount of an electrolyte in the use process is reduced and the service life of the battery can be prolonged; and furthermore, the odds of unsafe accidents such as explosion and the like are reduced to a certain extent.

The invention discloses a negative plate of a lead-carbon battery and a preparation method thereof. The negative plate consists of lead powder, active carbon, carbon black, barium sulfate, sodium lignosulfonate, humic acid, short fiber and sulfuric acid. The battery prepared by the negative plate has the advantages that the charging acceptance can be effectively improved, the sulfation phenomenon of the negative electrode under high-rate partial state of charge (HRPSoC) is effectively relieved, the times of 2C charge-discharge rate circulation (3%DOD) under 50% state of charge can reach 18442, and compared with the traditional lead-acid storage battery, the cycle life can be prolonged by more than two times.

The invention discloses a negative plate of a battery, a preparation method thereof and the battery comprising the negative plate. The negative plate is composed of a plate grid and a negative pole material coated on the plate grid, and the negative pole material comprises a battery active material, a capacitor material as well as a conductive steric hindrance agent; the battery active material comprises 100 parts by weight of lead powder, 0.6-2.0 parts by weight of barium sulfate and 0.1-0.5 part by weight of short fiber, and the capacitor material comprises 0.1-10 parts by weight of active carbon; and the additive amount of the electric conduction steric hindrance agent is 0.1-5.0 in parts by weight, and the conductive steric hindrance agent comprises Magneli mutual sulfoxide titanium oxide and/or plumbous acid barium. The raw material of the negative plate of the battery provided by the invention can be used for postponing a negative board sulphate phenomenon through combining the three parts, the cold-starting property is markedly improved, and the heavy-current charge-discharge property is optimized.

A pasted positive nickel hydroxide electrode for use in battery cells (e.g., in nickel zinc cells, and nickel metal hydride cells) includes nickel hydroxide particles, a cobalt metal and/or cobalt compound and a sulfur-containing complexing agent capable of forming a complex with cobalt. The presence of the sulfur-containing complexing agent, such as dialkyldithiocarbamate (e.g., sodium diethyldithiocarbamate) improves lifetime and capacity utilization of the nickel electrode. The resulting pasted nickel hydroxide electrode includes a CoOOH conductive matrix after formation. The surface of the nickel hydroxide particles in the electrode is modified in some embodiments by providing a cobalt-containing coating onto the surface of the nickel hydroxide particles, followed by oxidation with a strong oxidizing agent. The complexing agent can be added before, after, or during the oxidation.

The invention discloses a lead-carbon battery for a motorcycle. The lead-carbon battery comprises positive grid, a positive lead plaster coated on the positive grid, a negative grid and negative lead plaster coated on the negative grid, wherein the positive lead plaster is prepared from the following raw materials in parts by weight: 100 parts of lead powder, 9-10 parts of dilute sulfuric acid which is 1.400 in density, 0.02-0.03 part of short fiber, 0.15-0.3 part of graphite and 13-14 parts of purified water; and the negative lead plaster is prepared from the following raw materials in parts by weight: 100 parts of lead powder, 0.95-1.15 parts of expanding agent, 1-4 parts of complex carbon material, 7-8 parts of dilute sulfuric acid which is 1.400 in density, 0.015-0.025 part of short fiber and 11-14 parts of purified water. The positive and negative active substance utilization ratio of the prepared lead-carbon battery for the motorcycle is increased by 15-25 percent in comparison to a conventional battery. When the battery is started for discharging at large current at the multiplying power of 8-10 times, the output power is stable.

The invention relates to negative pole lead paste for a lead-carbon super storage battery. The lead paste is prepared by mixing solid raw materials consisting of 1 to 93 percent of lead powder and 2 to 95 percent of lead-carbon composite material by using a paste mixing machine via a dry-mixing method and a wet-mixing method. The lead-carbon composite material of the negative pole lead paste for the lead-carbon super storage battery is prepared by the electro-deposition method and contains 25 to 55 weight parts of lead. The negative pole lead paste can increase the porosity and the utilization rate of negative pole active substances, improve the contraction state of a negative polar plate and enhance the bonding force between the lead paste and the polar plate as well as between the lead powder and the active carbon with high specific area, functions like a negative pole lead paste super capacitor under the condition of high carbon-added quantity, and improves the comprehensive performance of the storage battery.

The invention discloses rare-earth lead alloy for a lead-acid storage battery positive grid. The rare-earth lead alloy is characterized by being prepared by smelting the following component materials by weight percent: 0.01 to 0.12 percent of calcium, 1.2 to 2.0 percent of tin, 0.02 to 0.05 percent of aluminum, 0.01 to 0.12 percent of lanthanum, 0.01 to 0.12 percent of yttrium, 0.02 to 0.15 percent of cerium and the balance being lead. The rare-earth lead alloy is stable in chemical property, good in mobility, excellent in conductivity and strong in corrosion resistance; a lead-acid storage battery which is assembled by the grid is long in cycling life, strong in current discharging capacity and strong in charging acceptance capacity.

The invention is a self-cross-linked polyvinyl butyral (PVB) binder for organic photoconductors (OPC's) used in electrophotography. The no cross-linked form of the binder is available from Monsanto Co. in the U.S.A. a Butvar TM , and from Sekisui Chemical Co. in Japan as Slek TM . I discovered that the PVB may be self-cross-linked by subjecting it to a thermal cure at between about 150 DEG -300 DEG C. for about 2 hours. I think other ways of cross-linking, for example, e-beam, UV or X-ray radiation, will achieve results similar to those I obtained with heat. No cross-linker, nor cross-linkable copolymer nor catalyst is required to accomplish the cross-linking. After self-cross-linking, the PV has good mechanical durability and good anti-solvent characteristics. In addition, he self-cross-linked PVB's glass transition temperature (Tg) increases from about 65 DEG C. to about 170 DEG C. Also, when conventional photoconductor pigments are dispersed in the self-cross-linked PVB, they are well dispersed, and the resulting OPC's have good charge acceptance, low dark decay, and, in general, good photodischarge characteristics. Also, OPC's with the self-cross-linked PVB exhibited improved adhesion, so multi-layered OPC's made according to this invention will hav improved inter-layer bonding and longer economic lives.