Abstract: A manufacturing system includes equipment adapted to produce a flexible ribbon product, a control device adapted to control working parameters of the production equipment, and a signal adjustment device adapted to adjust control signals of the control device online and in real time to adjust the working parameters. The signal adjustment device includes a visual device for capturing online and real-time images of the flexible ribbon product produced by the production equipment, and a computer. The computer includes a calculation module adapted to calculate an offset distance between an insulation film on the produced flexible ribbon product and a forming area online and in real-time based on the captured images, and an adjustment module adapted to adjust the control signals of the control device online and in real-time based on the calculated offset distance until the offset distance is equal to zero.

Abstract: The present invention provides a low pressure anion exchange chromatography—turbidimetric method for simultaneous online analysis of trace S2? and Cl? in water samples using an apparatus comprising a low pressure pump, a sample valve, a sample loop, a low pressure anion chromatographic column, a reactor, an optical flow cell, an optical detector, a computer system, a mixer, a sample flow path, a propelling solution flow path, and a color developer solution flow path, the method comprising: (a) mapping a baseline; (b) mapping spectrogram of S2? and Cl? in test samples; (c) mapping standard working curves; and (d) calculating the concentrations of S2? and Cl? in the test samples based on the peak heights of S2? and Cl? in the spectrogram and the regression equations of standard working curves.

Abstract: The invention relates to an apparatus for simultaneous online assay of nitrites and nitrates in water samples with improved sensitivity and accuracy, enhanced capacity of anti-interference against salinity, reduced assay costs, and simplified operation.

Abstract: The invention relates to an apparatus for simultaneous online assay of nitrites and nitrates in water samples with improved sensitivity and accuracy, enhanced capacity of anti-interference against salinity, reduced assay costs, and simplified operation.

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: 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.