Abstract: A device for recovering electric energy in an AC motor-driven electric vehicle. The device includes a battery, a single-phase or three-phase inverter, a single-phase or three-phase inductor, an AC motor, a rectifier bridge or a second inverter, and a charger. The anode and the cathode of the battery are connected to input ends of the inverter, respectively. An output end of the inverter is connected to the AC motor via a primary coil of the inductor. An output end of a secondary coil of the single-phase or three-phase inductor is connected to an input end of the rectifier bridge or the second inverter. Output ends of the rectifier bridge are connected to the anode and the cathode of the battery, respectively. The charger is connected to the anode and the cathode of the battery for supplying power from an external power supply.

Abstract: A device for recovering electric energy in a DC motor-driven electric vehicle. The device includes a battery; a first inverter; an inductor; a first rectifier bridge or a second inverter; a DC motor; a second rectifier bridge or a third inverter; and a charger. The anode and the cathode of the battery are connected to input ends of the first inverter, respectively. One output end of the first inverter is connected to one end of a primary coil of the inductor. Another output end of the first inverter is connected to one input end of the first rectifier bridge or the second inverter. Another end of the primary coil of the inductor is connected to another input end of the first rectifier bridge. The charger is connected to the anode and the cathode of the battery for supplying power from an external power supply.

Abstract: A method for torrefaction of lignocellulosic biomass using a torrefaction reactor vessel having stacked trays, the method including: continuously feeding the biomass to an upper inlet of the torrefaction reactor vessel such that the biomass material is deposited on an upper tray of a plurality of trays stacked vertically within the reactor; as the biomass moves across an upper surface of each of the trays, heating and drying the biomass material with a gas injected into the vessel, wherein the gas is substantially non-oxidizing of the biomass, is under a pressure of at least 20 bar gauge and at a temperature of at least 200° C.; cascading the biomass down through the trays by passing the biomass through an opening in each of the trays to deposit the biomass on a lower tray; discharging torrefied biomass from a lower outlet of the torrefaction reactor vessel, and circulating gas extracted from a lower elevation of the reactor vessel to an upper region of the reactor vessel.

Abstract: A method for assaying anionic detergents in seawater comprises: (1) flow a sample through a sample system and an analysis-detection system; flow a reference solution through a reference system, a valve, and the analysis-detection system; where the sample and reference are mixed; and flow the mixture into an optical cell to produce a baseline, (2) flow a sample through the sample system and analysis-detection system; flow a buffer through a buffer system and a color developing system; where the buffer and a color developer are mixed; and flow the resulting mixture through the valve and analysis-detection system; where the sample is mixed with the buffer and developer mixture; and flow the resulting mixture into the cell to produce the sample spectrogram, (3) repeat (1) and (2) with standards of known detergent concentrations for corresponding spectrograms, and (4) compare the sample spectrogram with the standard spectrograms to determine the sample detergent content.

Abstract: A process for simultaneous assay of chlorides and sulfides by low pressure ion exclusion chromatography is provided, and in said process an analytic apparatus comprising a sampling valve, a sampling loop, an ion exclusion column and an analytic detection flow path is used, and said process comprises the following steps: (1) in the analytic detection flow path, the mixture of developer R1 and developer R2 mixes with Eluent C and then enters into a reactor, and the mixing is continued under heating.

Abstract: A process for simultaneous assay of chlorides and sulfides by low pressure ion exclusion chromatography is provided, and in said process an analytic apparatus comprising a sampling valve, a sampling loop, an ion exclusion column and an analytic detection flow path is used, and said process comprises the following steps: (1) in the analytic detection flow path, the mixture of developer R1 and developer R2 mixes with Eluent C and then enters into a reactor, and the mixing is continued under heating.

Abstract: Antenna amplifiers and automobile top antenna devices are provided. The antenna amplifier includes an AM frequency selection circuit, an AM signal amplification circuit, an FM frequency selection circuit, an FM signal amplification circuit, and a power circuit. The antenna amplifier is further provided with a trap circuit that has an end connected to the ground terminal of the antenna amplifier, and another end connected to a metal mounting base for an antenna on the automobile top. The antenna device includes a shark-fin antenna case, a metal mounting base, an antenna support and a radio receiving antenna. The antenna case is mounted on the metal mounting base to form an internal accommodation space in which the antenna support, the radio receiving antenna and a circuit board with an antenna amplifier are provided.

Abstract: A method for assaying anionic detergents in seawater comprises: (1) flow a sample through a sample system and an analysis-detection system; flow a reference solution through a reference system, a valve, and the analysis-detection system; where the sample and reference are mixed; and flow the mixture into an optical cell to produce a baseline, (2) flow a sample through the sample system and analysis-detection system; flow a buffer through a buffer system and a color developing system; where the buffer and a color developer are mixed; and flow the resulting mixture through the valve and analysis-detection system; where the sample is mixed with the buffer and developer mixture; and flow the resulting mixture into the cell to produce the sample spectrogram, (3) repeat (1) and (2) with standards of known detergent concentrations for corresponding spectrograms, and (4) compare the sample spectrogram with the standard spectrograms to determine the sample detergent content.

Abstract: The present invention relates to a column packing and concentrating columns for the analysis of metallic elements, wherein the column packing is formed from swollen and cleaned macroporous adsorbent resins of high, medium or non-polarity via dynamic on-column treatment or static immersion treatment using treating solution I or treating solution II; said treating solution I is a mixed aqueous solution of 0.02˜0.06 g/L of 2-(5-bromo-2-pyridyl azo)-5-diethylamino phenol, 1.60˜1.90 g/L of Na2B4O7.10H2O, 6.0×10?3˜8.0×10?3 mol/L of HCl, and polyethylene glycol octyl phenyl ether with a volume percent of 0.3˜0.8%; said treating solution II is a mixed aqueous solution of 0.04˜0.10 g/L of 2-(5-bromo-2-pyridyl azo)-5-diethylamino phenol, 0.05˜0.08 mol/L of glycin, 0.05˜0.08 mol/L of NaOH, 0.010˜0.015 mol/L of NaCl, and polyethylene glycol octyl phenyl ether with a volume percent of 0.3˜0.8%.

Abstract: A concentrating column useful for elemental analysis of trace metals consists mainly of column body, filtration membranes 6 fixed at the fluid inlet end and the outlet end of the column body, and column packing 8 packed inside the column body, wherein column packing 8 is prepared from the swollen and cleaned macroporous adsorbent resin of high, medium or non-polarity treated with a mixture of 3 mol/L NH4OH-1 mol/L HAC-3.0˜6.0×10?4 mol/L pyridin-(2-azo-4-)resorcin or a mixture of 0.5 mol/L Na2HPO4-1.0˜2.0×10?4 mol/L pyridin-(2-azo-4-)resorcin by dynamic on-column treatment or static immersion treatment. Two types of sample processing devices useful for elemental analysis of trace metals are provided with concentrating column employing the above-mentioned column packing.

Abstract: A concentrating column useful for elemental analysis of trace metals consists mainly of column body, filtration membranes 6 fixed at the fluid inlet end and the outlet end of the column body, and column packing 8 packed inside the column body, wherein column packing 8 is prepared from the swollen and cleaned macroporous adsorbent resin of high, medium or non-polarity treated with a mixture of 3 mol/L NH4OH-1 mol/L HAC-3.0˜6.0×10?4 mol/L pyridin-(2-azo-4-)resorcin or a mixture of 0.5 mol/L Na2HPO4-1.0˜2.0×10?4 mol/L pyridin-(2-azo-4-)resorcin by dynamic on-column treatment or static immersion treatment. Two types of sample processing devices useful for elemental analysis of trace metals are provided with concentrating column employing the above-mentioned column packing.