UV-Vis Spectrum Characteristics of Phycocyanin Purification in Water from Chao Lake.

Fresh blue algal from Chao Lake was used in this study. The crude extracts of phycocyanin were obtained with freeze-thaw method. The purification of phycocyanin was performed by combining two-step salt precipitation and two-step column chromatography. The reagent grade phycocyanin was achieved. Phycocyanin and impurity solution were obtained respectively in various stages subjected to the UV-Vis absorption spectrum scanning. With the development of the four-step purification process, the absorption peak of phycocyanin solution was redshifted from 260 to 280 nm in the wavelength range from 250 to 300 nm, and the maximum absorption peak of phycocyanin was redshifted from 617 to 620 nm in the wavelength range from 500nm to 700 nm. In the wavelength range from 250 to 700 nm, it showed that the impurity solution mainly contained impurity proteins and part of the phycocyanin in the first salting out, and mainly contained nucleic acids and vitamins substance in the second salting out. The first outflow components mainly contained phycoerythrin separated by the first column chromatography. The last outflow components mainly contained allophycocyanin separated by the second column chromatography. After the four-step purification process, the final purity of phycocyanin (A620/A280) is greater than 4,which met the standard of reagent grade．Thus it can be seen that two-step salt precipitation had a main function which was to remove impurity proteins, nucleic acids and vitamins substance, and two-step column chromatography main function was to remove phycoerythrin and allophycocyanin which were similar to phycocyanin.

[Characterization of Particle Size Distributions of the No-organized Lead Emission for a Lead and Zinc Smelter].

Using TH 880-F type dust tester and low pressure impactor (LPI), the size-segregated atmospheric particulates were collected, the particle size distribution characteristics and the content of lead were analyzed in the unorganized emission area (1 and 2) from the Blast and ISA furnaces within a lead-zinc smelter in Yunnan province. The results showed that lead in PM2.5(fine particulate matter, particle size <2.5 µm) accounted for 66.6% and 43.1% of PM10(particulate matter, particle size <10 µm) and TSP(total suspended particle, particle size<100 µm) in unorganized emission area 1, and the corresponding proportions in the unorganized emission area 2 were 54.1% and 38.7%, all these showed that the lead pollution mainly existed in small size particles. There was a close correlation between the lead content in the unorganized emission particulate matter and the wind direction and wind speed in the surface meteorological data, followed by the wind energy density. In lead smelting area, the correlation of lead content in the unorganized emission particulate matter with the wind direction and wind speed was the highest, followed by the wind energy density w. In the slag field, the correlation between lead content in the unorganized emission particulate matter and the vertical distribution of the temperature (γ) of the boundary layer was the highest, followed by the component u and v, and then the wind energy density w.

Cloud point extraction combined with high-performance liquid chromatography for speciation of chromium(III) and chromium(VI) in environmental sediment samples.

A sensitive and simple method for high-performance liquid chromatography (HPLC) determination of traces of chromium species in lake sediments after preconcentration by cloud point extraction (CPE) has been developed. Simultaneous preconcentration of Cr(III) and Cr(VI) in sediment samples was achieved by CPE with 1-(2-thiazolylazo)-2-naphthol (TAN) as the chelating agent and non-ionic surfactant octylphenoxypolyethoxyethanol (Triton X-114) as the extractant. Baseline separation of the TAN chelates of Cr(III) and Cr(VI) was realized on a RP-C(18) column by using a mixture of methanol-water (69:31, v/v) solution and 4.5 mmol L(-1) CTMAB buffered with 0.03 mol L(-1) NaAc-HAc solution (pH 5.5) as the mobile phase at a flow rate of 0.8 mL min(-1). The variables affecting the complexation and extraction steps were examined. The precision (R.S.D.) for seven replicate injections of a mixture of 100 microg L(-1) of Cr(III) and Cr(VI) was 1.2 and 0.9% for the retention time, 4.7 and 2.7% for the peak area, respectively. The concentration factor was 45 for Cr(III) and 40 for Cr(VI). The detection limit (LOD) of this method, calculated as three times the standard deviation of the blank signals was 7.5 microg L(-1) for Cr(III) and 3.5 microg L(-1) for Cr(VI), respectively. The proposed procedure was applied to the speciation of chromium in sediment samples with satisfactory results.

Photochemistry in the mixed aqueous solution of nitrobenzene and nitrous acid as initiated by the 355 nm UV light.

The 355 nm photon-initiated microscopic reaction mechanisms of the mixed aqueous solution of nitrobenzene and nitrous acid in the presence or absence of O(2) were studied by the laser flash photolysis technique. The main transient absorption peaks in the recorded spectra were assigned and the growth/decay trends of several transient species were investigated. It was found that the OH radical formed from the photolysis of nitrous acid triggered most of the subsequent radical reactions. The rate constant of the reaction between OH radical and nitrobenzene was measured to be (3.4 +/- 0.1) x 10(9) l mol(-1) s(-1). The product from this reaction, namely C(6)H(5)NO(2)-OH adduct, was found to react with O(2) to yield C(6)H(5)NO(2)-OHO(2) adduct with a rate constant of (1.6 +/- 0.2) x 10(9) l mol(-1) s(-1). Final steady-state products were identified by GC/MS analysis and were in accordance with the transient spectroscopic results. The possible reaction pathways were proposed.