This method for diagnosing a battery pack having a configuration in which a plurality of cells are connected in series, using a system for obtaining detected data including the current and temperature of the battery pack and the voltage of each cell, includes: a step of calculating an electric charge capacity and a state of charge (SOC) of each cell, using the current and the temperature, the voltage of each cell, an open circuit voltage (OCV) - SOC function, and an OCV - resistance table, and calculating an amount of unbalance, which is an estimated value of the SOC, and the resistance for each cell when the battery pack is fully charged; and a step of calculating the energy capacity of the battery pack using the electric charge capacity, the amount of unbalance, and the resistances. As a result, the energy capacity of the battery pack can be calculated accurately, even in an unbalanced state.
H01M 10/48 - Accumulators combined with arrangements for measuring, testing or indicating the condition of cells, e.g. the level or density of the electrolyte
B60L 53/10 - Methods of charging batteries, specially adapted for electric vehicles; Charging stations or on-board charging equipment therefor; Exchange of energy storage elements in electric vehicles characterised by the energy transfer between the charging station and the vehicle
B60L 58/12 - Methods or circuit arrangements for monitoring or controlling batteries or fuel cells, specially adapted for electric vehicles for monitoring or controlling batteries responding to state of charge [SoC]
B60L 58/16 - Methods or circuit arrangements for monitoring or controlling batteries or fuel cells, specially adapted for electric vehicles for monitoring or controlling batteries responding to battery ageing, e.g. to the number of charging cycles or the state of health [SoH]
G01R 31/382 - Arrangements for monitoring battery or accumulator variables, e.g. SoC
G01R 31/385 - Arrangements for measuring battery or accumulator variables
G01R 31/387 - Determining ampere-hour charge capacity or SoC
G01R 31/389 - Measuring internal impedance, internal conductance or related variables
G01R 31/392 - Determining battery ageing or deterioration, e.g. state of health
H02J 7/02 - Circuit arrangements for charging or depolarising batteries or for supplying loads from batteries for charging batteries from ac mains by converters
2.
REAGENT VESSEL HOLDER FOR AN ANALYTICAL INSTRUMENT, REAGENT SUPPLY SYSTEM FOR AN ANALYTICAL INSTRUMENT AND AN ANALYTICAL INSTRUMENT
A reagent vessel holder (110) for an analytical instrument is disclosed by the present invention. The reagent vessel holder (110) comprises at least one reagent vessel compartment (112) for receiving a reagent vessel (154), wherein the reagent vessel compartment (112) comprises a base (114) and at least two lateral guiding elements (130), and at least one hollow needle (120) for piercing the reagent vessel (154), wherein the hollow needle (120) is disposed on a front end (122) of the reagent vessel compartment (112) near the base (114) and extends in a direction substantially parallel to the base (114), wherein the lateral guiding elements (130) are disposed so as to be adapted to slidably guide the reagent vessel (154) in a direction substantially parallel to the direction, in which the hollow needle (120) extends, wherein the lateral guiding elements (130) are adapted to receive the reagent vessel (154) therebetween and are biased towards one another. Further, a reagent supply system for an analytical instrument and an analytical instrument comprising such a reagent vessel holder (110) are disclosed by the present invention.
JAPAN AS REPRESENTED BY DIRECTOR GENERAL OF NATIONAL REHABILITATION CENTER FOR PERSONS WITH DISABILITIES (Japan)
HITACHI HIGH-TECH CORPORATION (Japan)
Inventor
Kato, Seishi
Kimura, Tomoko
Ohtoko, Kuniyo
Abstract
A method for synthesizing cDNA possessing a consecutive sequence starting with a nucleotide adjacent to a cap structure of mRNA, which comprises (i) a process for annealing a double-stranded DNA primer and an RNA mixture containing mRNA possessing a cap structure, (ii) a process for preparing a conjugate of an mRNA/cDNA heteroduplex and a double-stranded DNA primer by synthesizing the first-strand cDNA primed with the double-stranded DNA primer using reverse transcriptase, and (iii) a process for circularizing the conjugate of the mRNA/cDNA heteroduplex and the double-stranded DNA primer by joining the 3' and 5' ends of the DNA strand containing cDNA using ligase. This method enables us to efficiently synthesize a full- length cDNA possessing a consecutive sequence starting with a transcription-start- site nucleotide from a small amount of RNA by small processes.