锡(Sn)的微量分析方法

提出了苯芴酮比色法分析溶液中微量Sn,测定Sn量的范围为3～40ppm。

Effect of Organic Ligands on Biological Availability of Inorganic Phosphorus in Soils

Citrate, oxalate, tartrate and malate were added into soils during the growthperiod of ryegrass to study the effect of different organic ligands on the release of variousinorganic P (Pi) fractions in a yellow-brown soil and a paddy soil. The results showed that oxalatewas most effective in promoting the release of total Pi in the yellow-brown soil and tartrate in thepaddy soil. The dominant Pi fractions released from the yellow-brown soil were calcium phosphate(Ca-P) and aluminum phosphate (Al-P) and those from the paddy soil were iron phosphate (Fe-P) andreductant soluble phosphate (O-P) mobilized by tartrate. Phosphorous-mobilizing capability oforganic acids in the yellow-brown soil revealed the following order: oxalate > citrate > malate >tartrate. In the paddy soil, the order was tartrate > citrate ≈ oxalate > malate. It wasdemonstrated that organic ligands were different in their capabilities of mobilizing Pi and the sameorganic ligand showed also a discrepancy in mobilizing P in different soils. Although the additionof organic ligands into soils could increase the amount of P taken up by ryegrass, the more uptakeof P, however, was not only due to the more release of Pi, but also partly from organic P. In manycases, organic ligands promoted the release of the total Pi, while different fractions showeddifferent trends: some increased and others decreased.

Adsorption of Acid Phosphatase on Minerals and Soil Colloids in Presence of Citrate and Phosphate

The aim of this work was to study the influence of phosphate and citrate, which are common inorganic and organic anions in soils, on the adsorption of acid phosphatase by kaolin, goethite and the colloids separated from yellow-brown soil (YBS) and latosol (LS) in central-south China. The YBS colloid has the major clay mineral composition of 1.4 nm mineral, illite and kaolinite while the LS colloid mainly contains kaolinite and oxides. The adsorption isotherm of acid phosphatase on the examined soil colloids and minerals fitted to the Langmuir model. The amount of enzyme adsorbed in the absence of ligands was in the order of YBS colloid > LS colloid > kaolin ≈ goethite. In the presence of phosphate or citrate, the amounts of the enzyme adsorbed followed the sequence YBS colloid > kaolin > LS colloid > goethite. The presence of ligands also decreased the binding energy between the enzyme and soil colloids or minerals. With the increase of ligand concentration from 10 mmol L-1 to 400 m mol L-1, different behaviors for the adsorption of enzyme were found in the colloid and mineral systems studied. A sharp decrease in enzyme adsorption was observed on goethite while gradual decreases of enzyme adsorption were recorded in the two soil colloid systems. However, no any decrease was found for the amount of enzyme adsorbed on kaolin at higher ligand concentrations. When phosphate or citrate was introduced to the system before the addition of enzyme, the ligands usually enhanced the adsorption of enzyme. The results obtained in this study suggested the important role of kaolinite mineral in the adsorption of enzyme molecules in acidic soils in the presence of various ligands.

Adsorption property of citrate dispersant on BaTiO_3 particles in aqueous solution

Dispersion behavior of ultra fine BaTiO3 particles in the aqueous solution of ammonium citrate （NH4-CA） or citric acid lanthanum chelate （NH4-La-CA） was investigated. The dispersion property was characterized with sedimentation value. It is easier to obtain well dispersed slurry with NH4La-CA than NH4-CA. In an attempt to better understand the role of citric acid radical, simulation of the dispersant adsorption on BaTiO3 particle was performed with universal force field （UFF）. It is demonstrated that the interaction between citric acid radical and BaTiO3 particle surface is a weak chemical adsorption. Trivalent citric acid radical is adsorbed on BaTiO3 particle surface with maximal adsorption energy. And, larger molecules of NH4-La-CA formed by adding La^3＋ lead to better dispersion property than NHn-CA.

Synthesis and Study of Glutamine Acid Containing Citrates

Terms of synthesis were defined for the creation of new generation chelate fertilizers and for their experimental testing. Glutamine acid and citric acid containing chelate citrates of the general formulae M.gI.HL＇nHO were synthesized, where, M = Mn, Zn, Fe, Co, Cu; n = 0; 1; 1.5; gl-glutamine acid; HL-citric acid anion. Identity and composition of synthesized compounds were determined by microelemental analysis, melting temperature and X-ray diffraction analysis. X-ray diffraction analysis of the compounds and glutamine acid and citric acid （H4L） was used to determine their crystalline structure and roentgen-amorphous and iso-structural orders. Their solubility was studied in various solvents.

Nitrate Removal from Drinking Water with Sodium Citrate as Sole Carbon Source

This paper investigates the effect of using sodium citrate（NaC6H5O6·2H2O）as sole carbon source for nitrate removal from drinking water.With sodium citrate as sole carbon source, batch experiments have been conducted to study the law of denitrification influenced by pH, C/N and temperature. Results show that a denitrification rate reaching 1.32 g NO-3-N /（g Biomass·d） was obtained when pH was at 7.5,C/N at 1.7（atom ratio）, and temperature from 20 ℃ to 30 ℃. The results also show that denitrification rate with sodium citrate as carbon source approaches to that with methanol as carbon source.

Citric Acid-Enhanced Electroremediation of Toxic Metal-Contaminated Dredged Sediments： Effect of Open/Closed Orifice Condition, Electric Potential and Surfactant

Citric acid(CA), a widely used eco-friendly electrolyte, can be employed as an agent for enhancing toxic metal(TM) removal from contaminated dredged sediment using electrokinetic(EK) technology. In this study, dredged harbor sediments co-contaminated by TMs were subjected to enhanced EK treatment using a mixture of chelating agent(CA) and surfactant as an additive in the processing fluids. Several control conditions that may influence the efficiency of TM removal were tested, including open/closed sediment chamber orifices, electric potential gradients(0.5, 1.0, and 1.5 V cm^(-1)), and electrolyte surfactant. Tween 20(4 mmol L-1) was used as a surfactant within the electrolyte to investigate the extent of TM removal in sediment with high organic matter content. The results showed that an open orifice led to a greater electro-osmotic flow(EOF) with moderate TM removal. In contrast, a closed orifice with a nonionic surfactant electrolyte allowed the highest removal of TMs from the matrix. Moreover, increasing the electric potential gradient led to a higher EOF under the open orifice condition, but no significant increase in TM removal was observed owing to a higher accumulation of TMs in the middle of the matrix, caused by the opposite direction of EOF and electro-migration of metal-citrate complexes.