1314 results about "Discharge rate" patented technology

Nanocomposite materials comprising a metal oxide bonded to at least one graphene material. The nanocomposite materials exhibit a specific capacity of at least twice that of the metal oxide material without the graphene at a charge / discharge rate greater than about 10C.

Positive electrode active materials are formed with various metal oxide coatings. Excellent results have been obtained with the coatings on lithium rich metal oxide active materials. Surprisingly improved results are obtained with metal oxide coatings with lower amounts of coating material. High specific capacity results are obtained even at higher discharge rates.

Positive electrode active materials are described that have a high tap density and high specific discharge capacity upon cycling at room temperature and at a moderate discharge rate. Some materials of interest have the formula Li1+xNiαMnβCoγO2, where x ranges from about 0.05 to about 0.25, α ranges from about 0.1 to about 0.4, β ranges from about 0.4 to about 0.65, and γ ranges from about 0.05 to about 0.3. The materials can be coated with a metal fluoride to improve the performance of the materials especially upon cycling. Also, the coated materials can exhibit a very significant decrease in the irreversible capacity lose upon the first charge and discharge of the battery.

Lithium ion secondary batteries are described that have high total energy, energy density and specific discharge capacity upon cycling at room temperature and at a moderate discharge rate. The improved batteries are based on high loading of positive electrode materials with high energy capacity. This capability is accomplished through the development of positive electrode active materials with very high specific energy capacity that can be loaded at high density into electrodes without sacrificing performance. The high loading of the positive electrode materials in the batteries are facilitated through using a polymer binder that has an average molecular weight higher than 800,000 atomic mass unit.

A lithium-ion battery is provided that has a fast charge and discharge rate capability and low rate of capacity fade during high rate cycling. The battery can exhibit low impedance growth and other properties allowing for its use in hybrid electric vehicle applications and other applications where high power and long battery life are important features.

Systems and methods for providing multiple pass continuous flow dialysis therapy are provided. The present invention includes a fluid circuit connected to a patient via a catheter thereby defining a fluid loop along which a therapy fluid including a dialysate can be continuously circulated into, through and out of a peritoneal cavity of a patient to remove a therapeutically effective amount of excess water and solutes including uremic toxins. The feed rate and discharge rate of therapy fluid into the fluid loop can be controllably regulated in proportion to the circulation rate of fluid in the fluid loop such that the therapy fluid can pass a multiple number of times along the fluid loop prior to discharge.

An energy storage system includes a vanadium redox battery that interfaces with a control system to optimize performance and efficiency. The control system calculates optimal pump speeds, electrolyte temperature ranges, and charge and discharge rates. The control system instructs the vanadium redox battery to operate in accordance with the prescribed parameters. The control system further calculates optimal temperature ranges and charge and discharge rates for the vanadium redox battery.

A programmed microcontroller based sump pump system includes multiple pumps that can be employed with one as a primary pump and one as a back-up, or can be employed in combination to increase the discharge rate. The microcontroller monitors the back-up battery condition, and computes and displays the battery life; monitors the system for clogs or vapor locks in the discharge piping; switches to an emergency periodic pumping mode of operation, when needed; and notifies the user by phone or e-mail of a system malfunction.

Batteries with high energy and high capacity are described that have a long cycle life upon cycling at a moderate discharge rate. Specifically, the batteries may have a room temperature fifth cycle discharge specific energy of at least about 175 Wh / kg discharged at a C / 3 discharge rate from 4.2V to 2.5V. Additionally, the batteries can maintain at least about 70% discharge capacity at 1000 cycles relative to the fifth cycle, with the battery being discharged from 4.2V to 2.5V at a C / 2 rate from the fifth cycle through the 1000th cycle. In some embodiment, the positive electrode of the battery comprises a lithium intercalation composition with optional metal fluoride coating. Stabilizing additive maybe added to the electrolyte of the battery to further improve the battery performance. The batteries are particularly suitable for use in electric vehicles.

Positive electrode active materials comprising a dopant in an amount of 0.1 to 10 mole percent of Mg, Ca, Sr, Ba, Zn, Cd or a combination thereof are described that have high specific discharge capacity upon cycling at room temperature and at a moderate discharge rate. Some materials of interest have the formula Li1+xNiαMnβ-δCoγAδXμO2−zFz, where x ranges from about 0.01 to about 0.3, δ ranges from about 0.001 to about 0.15, and the sum x+α+β+γ+δ+μ can approximately equal 1.0. The materials can be coated with a metal fluoride to improve the performance of the materials especially upon cycling. The materials generally can have a tap density of at least 1.8 g / mL. Also, the materials can have an average discharge voltage of around 3.6 V.

Positive electrode active materials are described that have a very high specific discharge capacity upon cycling at room temperature and at a moderate discharge rate. Some materials of interest have the formula Li1+xNiαMnβCOγO2, where x ranges from about 0.05 to about 0.25, α ranges from about 0.1 to about 0.4, β ranges from about 0.4 to about 0.65, and γ ranges from about 0.05 to about 0.3. The materials can be coated with a metal fluoride to improve the performance of the materials especially upon cycling. Also, the coated materials can exhibit a very significant decrease in the irreversible capacity lose upon the first charge and discharge of the cell. Methods for producing these materials include, for example, a co-precipitation approach involving metal hydroxides and sol-gel approaches.

Lithium ion batteries having an anode comprising at least one graphene layer in electrical communication with titania to form a nanocomposite material, a cathode comprising a lithium olivine structure, and an electrolyte. The graphene layer has a carbon to oxygen ratio of between 15 to 1 and 500 to 1 and a surface area of between 400 and 2630 m2 / g. The nanocomposite material has a specific capacity at least twice that of a titania material without graphene material at a charge / discharge rate greater than about 10 C. The olivine structure of the cathode of the lithium ion battery of the present invention is LiMPO4 where M is selected from the group consisting of Fe, Mn, Co, Ni and combinations thereof.

Lithium ion batteries can be activated and then cycled to exploit a moderate fraction of the discharge cycling capacity such that the discharge capacity and average discharge voltage stay within initial values for thousands of cycles. The superior cycling performance has been achieved at relatively high discharge rates and for practical battery formats. Lithium ion battery performance can also be achieved with superior cycling performance with partially activated batteries such that good discharge capacities can be exploited for many thousands of cycles before the discharge capacity and average discharge voltage drops more than 20% from initial values. The positive electrode active material can be a lithium rich metal oxide. The activation of the battery can comprise phase changes of the active materials. As described herein, the phase changes can be manipulated to exploit a reasonable fraction of the available high capacity of the material while providing outstanding cycling stability.

The present invention provides a high current pulse generator for DC powered devices. The generator includes batteries as the power source that charges supercapacitors as well as provides power to the loads as required. During charging, the supercapacitors are connected in parallel, but they are switched to series connection by relays at the moment that the loads demand large currents. No other controlling means except for relays in the circuit is employed, so that the electric arrangement is simple, reliable, and cost-effective. As the batteries are designed to deliver currents at low discharge rates, the effective use-time of batteries is prolonged. Furthermore, due to the high power densities of supercapacitors, the readily available alkaline batteries can be utilized in the power unit for electric power tools.

Positive electrode active materials are formed with various metal oxide coatings. Excellent results have been obtained with the coatings on lithium rich metal oxide active materials. Surprisingly improved results are obtained with metal oxide coatings with lower amounts of coating material. High specific capacity results are obtained even at higher discharge rates.

The invention relates to a method for extracting gas in low air permeability coal layer by pulse fracture anti-reflection, comprising the following steps: firstly using the blast-proof pulse-type coal layer high pressure water injector with adjustable frequency and pressure from the coal layer, high tunnel or low tunnel; using the pulse water effect generated by the periodical change of high pressure pulse water inside the drill hole of coal body, wherein the maximum pulse pressure is 35 MPa, the flow is about 300 L / min, and the pulse frequency is 0-1460 times / min; forcing the macroscopic fracture in the coal layer to be expanded and communicated; promoting the micro-pore fracture to be formed and extended; forming a new regeneration fracture net; providing a permeable channel of water inthe coal layer so as to achieve the effects of improving the mechanical property of the coal body, reducing the stress of the coal body in front of the working face and improving the discharge rate of the gas. Through the method, the pressure releasing range of the coal layer is enlarged, the whole pressure is adequately released, the radius of influence range of fracture can reach 10-40 m, and the air permeability of the coal body can be improved by 100-1000 times; and the method is simple, easy to operate and good in effect.

The present invention provides electrochemical cells capable of good electronic performance, particularly high specific energies, useful discharge rate capabilities and good cycle life. Electrochemical cells of the present invention are versatile and include primary and secondary cells useful for a range of important applications including use in portable electronic devices. Electrochemical cells of the present invention also exhibit enhanced safety and stability relative to conventional state of the art primary lithium batteries and lithium ion secondary batteries. For example, electrochemical cells of the present invention include secondary electrochemical cells using anion charge carriers capable of accommodation by positive and negative electrodes comprising anion host materials, which entirely eliminate the need for metallic lithium or dissolved lithium ion in these systems.

A solid electrolyte including a composition represented by Formula 1 below is provided: aLi2O-bB2O3-cM-dX (1) wherein M is at least one selected from the group consisting of TiO2, V2O5, WO3, and Ta2O5; X is at least one selected from LiCl and Li2SO4; 0.4<a<0.55; 0.4<b<0.55; 0.02<c<0.05; a+b+c=1, and 0≦d<0.2. A method for preparing the solid electrolyte and a battery using the solid electrolyte are also provided. The solid electrolyte exhibits high ionic conductivity. Lithium and thin film batteries using the solid electrolyte are improved in charge / discharge rate, power output, and cycle life.

Disclosed herein is a cylindrical secondary battery including a cap assembly constructed in a structure in which a vent, which intercepts electric current and discharges pressurized gas when the interior pressure of the battery is increased due to abnormal operation of the battery, is in contact with a top cap having a protruding central part, wherein the end of the vent is bent to surround the outer circumferential surface of the top cap, and a groove for preventing the leakage of an electrolyte and preventing the occurrence of defectiveness of the battery during the assembly of the battery is formed at interfaces between the vent and the top cap such that the groove is arranged in parallel with the outer circumferential surface of the top cap. The secondary battery according to the present invention has the effect of accomplishing high charging and discharging rate, providing uniform output even when external physical impacts, such as vibration or dropping, are applied to the secondary battery, and preventing the occurrence of defectiveness during the assembly of the secondary battery. Furthermore, the leakage of the electrolyte out of the battery is restrained under these conditions. Consequently, the secondary battery according to the present invention can be preferably used as a high-output power source.

Systems for controlling the in-feed and discharge rates of materials flowing into and out of a mixing process where one priority is to achieve a target mixture flow rate from the mixing process and another priority can be to achieve a target value for a mixture property. Actuators can be operated to control material in-feed rates, the mixture composition, and discharge rate, and can maintain a hold-up of the mixture in the mixing process. A total flow rate controller provides a control signal to a controller acting on the discharge rate and a controller acting on the in-feed rates. The mixture discharge flow rate can be automatically reduced from its desired target when the commanded rate of at least one of the materials exceeds its available supply rate as inferred from an inability to maintain the targeted value for the mixture property.

Disclosed is a piezoelectric pump. The piezoelectric pump includes a pump body, a drive unit, a detection section, and a control unit. The pump body includes a hole for introducing a fluid from outside thereinto and jetting the fluid from inside, a wall portion disposed so as to face the hole, and a piezoelectric body provided on the wall portion to vibrate the wall portion. The drive unit drives the piezoelectric body. The detection section detects a signal corresponding to a discharge rate of the fluid from the hole. The control unit controls a drive voltage and a drive frequency of the drive unit on the basis of the signal.

Discharge rate control method for ink-jet printer 1 including film forming step forming film B on coating article 2 with non ink-absorbent characteristic by discharging ink on coating article 2 from a plurality of nozzles 4 of print head 3, film thickness measuring step measuring film thickness of film B, corresponding to ink discharge position of each nozzle 4, formed on coating article 2 in film forming step, and discharge rate correcting step correcting discharge rate of ink from each nozzle 4 by increasing or decreasing discharge rate based on difference between target film thickness Ba and film thickness at ink discharge position of each nozzle 4 measured in film thickness measuring step.

A cylinder driving system capable of reducing the number of hydraulic devices and the amount of energy loss and an energy regenerating method thereof are provided. To this end, the system includes i) a hydraulic cylinder, ii) a hydraulic pump having three suction / discharge ports of a first port for supplying oil to a bottom chamber of the hydraulic cylinder or draining oil from the bottom chamber, a second port for draining oil from a head chamber of the hydraulic cylinder or supplying oil to the head chamber, and a third port for draining oil from a tank or supplying oil to the tank, the suction rate or the discharge rate in the first port being the sum of the respective discharge rates or suction rates in the second port and the third port, and iii) a driving source for driving the hydraulic pump.

First and second hydraulic pumps each adapted to operate plural actuators are activated by separate electric motors respectively. In accordance with signals provided from a controller on the basis of operations of levers, the number of revolutions of the electric motor and that of the electric motor are controlled each independently and simultaneously to control the discharge rates of both hydraulic pumps.

Improved high energy capacity designs for lithium ion batteries are described that take advantage of the properties of high specific capacity anode active compositions and high specific capacity cathode active compositions. In particular, specific electrode designs provide for achieving very high energy densities. Furthermore, the complex behavior of the active materials is used advantageously in a radical electrode balancing design that significantly reduced wasted electrode capacity in either electrode when cycling under realistic conditions of moderate to high discharge rates and / or over a reduced depth of discharge.

The invention discloses a preparation method of an anode material for a power lithium ion battery. The preparation method comprises the following steps: by adopting petroleum coke ground until the grain size is 1-6mu m, calcined petroleum coke or needle coke as a raw material, adding additives, adding a mixture to a reaction kettle to carry out first high-temperature carbonization coating under the protection of the inert atmosphere, then grinding the mixture with a grinder until the grain size is 5-13mu m, then carrying out superhigh-temperature graphitization at a temperature above 3200 DEG C, adding one or a mixture of petroleum asphalt, coal asphalt and resin to a material obtained after graphitization, and then enabling the mixture to enter a carburization furnace to undergo second coating under the protection of the inert atmosphere to obtain the anode material for the power lithium ion battery, namely a spheroidal artificial graphite material which is formed through bonding after being coated with granules and undergoes two-time coating and three-time high-temperature treatment. The preparation method has the advantages that the discharge rate property of the anode material is improved, the low temperature properties of the anode material are improved, and the latest requirements of the market for the product are further met.

The present invention provides a lithium-containing composite oxide for a positive electrode for a lithium secondary battery, which has a large volume capacity density and high safety, and excellent durability for charge and discharge cycles and charge and discharge rate property, and its production method.The lithium-containing composite oxide is represented by the general formula LipNxMyOzFa (where N is at least one element selected from the group consisting of Co, Mn and Ni, M is at least one element selected from the group consisting of Al, Sn, alkaline earth metal elements and transition metal elements other than Co, Mn and Ni, 0.9≦p≦1.2, 0.965≦x<2.00, 0<y≦0.035, 1.9≦z≦4.2, and 0≦a≦0.05), wherein when a powder of the lithium-containing composite oxide is classified into small particles with an average particle size of 2 μm≦Ds50≦8 μm and large particles with an average particle size of 10 μm≦Dl50≦25 μm, a content of the small particles is from 15 to 40% by weight and a content of the large particles is from 60 to 85% by weight, and 0.01≦ys≦0.06, 0≦yl≦0.02 and 0≦yl / ys<1, where (ys) is a ratio of the M element in the above general formula in the small particles and (yl) is a ratio of the M element in the general formula in the Large particles.

Improved high energy capacity designs for lithium ion batteries are described that take advantage of the properties of high specific capacity anode active compositions and high specific capacity cathode active compositions. In particular, specific electrode designs provide for achieving very high energy densities. Furthermore, the complex behavior of the active materials is used advantageously in a radical electrode balancing design that significantly reduced wasted electrode capacity in either electrode when cycling under realistic conditions of moderate to high discharge rates and / or over a reduced depth of discharge.

The present invention is intended to provide a dispenser structure for aerosol containers, which can control the discharge rate of aerosol and ensure satisfactory and safe dispensing of the aerosol while preventing the particle size of the dispensed aerosol from becoming too fine and preventing its excessive scattering which too fine particles would entail. Its structure is characterized in that it includes a dispenser (1) provided with a dispensing guide or first nozzle (11) communicating with a dispensing valve (2); a second nozzle (10) provided within the dispensing guide or first nozzle (11) and having a smaller dispensing port (10a) whose bore d is not more than 0.5 mm; and a larger dispensing port (1a) having a bore b of 0.8 to 3 mm and a length c of not less than 5 mm, formed within the dispensing guide or first nozzle (11) downstream, in the direction of dispensing from the second nozzle (10).