Polycyclic Aromatic Hydrocarbons in Agricultural Soils of the Southern Subtropics,China

从到全球环境的污染的中国的副热带的区域的坚持的有机污染物(流行音乐) 的贡献被付了大注意；然而，很少在中国的这些区域以内在农业生态系统对流行音乐的国家被知道。这研究首先揭示了污染的国家和多不的芳族烃的分发(哼) 在在副热带的区域的农业土壤。115 表土(0 20 厘米) 在这些区域的胃被取样。集中和类型哼坚定的使用气体色层法被连接到质谱法(GCMS ) 。总数哼集中从 22.1 ～ 1 256.9 ng g ? 1，与 318.2 ±的一个平均数 148.2 ng g ? 1。措辞笼统地，水流哼集中比大多数哼低层次从不同国家和区域在很多调查报导了。哼异构体比率显示了那焦性没食子酸 lysin 的起源例如与车辆尾巴气体和工业排出物有关的石块燃料燃烧，是主导的来源在中国的南部的副热带的区域哼。尽管哼集中与减少的污染，人口，和交通密度减少了，在很大程度上哼作文在整个副热带的土壤是类似的与萘，菲， fluoranthene，和是主导的 benzo (b) fluoranthene。

Synthesis and Characterization of Ethylenediamine Tetraacetic Acid Tetrasodium Salt Loaded in Microcapsules with Slow Release Properties

The microcapsules with cores of ethylenediamine tetraacetic acid tetrasodium salt(Na4-EDTA)and walls of polyurea were synthesized via an interfacial polycondensation reaction with 2,4-tolylene diisocyanate as an oil-soluble monomer and diethyl triamine as a water-soluble monomer.Various manufacturing parameters,including the amount of emulsifier,agitation speed,stirring time and ratios of the wall materials to core materials,were altered to optimize process variables during the synthesis of microcapsules,and the effects of these parameters on the characteristics of the microcapsules were examined.The structure,morphology,mean particle size and size distribution were characterized by optical microscope and scanning electron microscopy(SEM),showing that the mean diameter of optimal microspheres was approximately 6μm,and microcapsules were spherical.In vitro release of Na4-EDTA from these microcapsules was performed in distilled water.Under the optimal preparation conditions, the Na4-EDTA release profiles were biphasic with a burst release followed by a gradual release phase.After an initial burst,a continuous Na4-EDTA release was up to 5-7 days.The optimal synthesis conditions for the microcapsules with stable,good morphology and good controlled-release properties were as follows:emulsifier Span-80 10% (by mass),agitation speed 900 r·min1,stirring time 30 min,and the ratio of the wall materials to core materials 0.15.

Distribution and deposition of polycyclic aromatic hydrocarbons in precipitation in Guangzhou, South China

Polycyclic aromatic hydrocarbons （PAHs） were measured in precipitation from March to August 2005 in Guangzhou, South China. Fourteen PAHs were studied, and their total concentrations varied from 616.6 to 3486.7 ng/L in dissolved phase and from 403.8 to 3125.5 ng/L in particulate phase. The estimated deposition loading of PAHs was 3568 ug/m^2 during the monitoring period. The deposition of PAHs was a potential source for Pearl River comparing with the contents of surface water. In addition, the high concentration in precipitation here implied that PAHs pollution was a potential environmental problem in Guangzhou. Most precipitation concentrations of PAHs in March （the last month in winter in Guangzhou） were higher than in the other months （in rainy season）. PAHs inclined to be adsorbed to particulate phase with the increase of molecular weight in rainwater. Combustion of fossil fuel and biomass might be the major source of PAHs, while the direct leakage or volatilization from petroleum products might be insignificant.

Photoelectrocatalytic properties and reactivity of Ti/Au-TiO_2 mesh electrodes

A kind of photoelectrode was innovated by anodising titanium mesh in H 2SO 4 solution and photo reduced in HAuCl 4 solution and named Ti/Au TiO 2 mesh electrode. The structural and surface morphology of the Ti/Au TiO 2 mesh was examined by X ray diffraction, laser Raman spectra, scanning electronic microscopy(SEM) and X ray photoelectron spectroscopy respectively. The results indicate that its crystal structure, morphology and the size of pore are affected greatly by gold deposition. XPS measurement shows that the valence band of Ti/TiO 2 has two peaks: a wide one at 4.97 eV and a narrow one at 6.61 eV, which correspond mainly to π(nonbonding) and σ (bonding) O 2p orbitals. The emission intensity of O 2p orbitals becomes stronger and the width of the valence band increases with the increase of Au content. And the emission of nonbonding shifts toward lower binding energy and that of bonding O 2p orbitals shifts toward higher binding energy. The photoelectrocatalytic(PEC) oxidation of humic acid(HA) was investigated in terms of TOC. The PEC oxidation efficiency of Ti/Au TiO 2 mesh with optimal content of gold is higher than that of Ti/TiO 2 mesh. It is suggested that the recombination of electrons and holes is hindered owing to gold deposition. The investigation shows that PEC oxidation is a convenient way to mineralize organic matter for water treatment.

Photocatalytic degradation of phenol in aqueous solution using TiO_2/Ti thin film photocatalyst

In order to clarify the respective role of the UV light, catalyst, external bias as well as their combined effects on the photodegradation process and to clarify the photocatalytic mechanism under different experimental conditions, a series of experiments were conducted in a shallow pond photoreactor with an effective volume of 100 mL using TiO 2/Ti thin film prepared by anodization as photocatalyst. A 300W UV lamp( E max =365 nm)was used as side light source. The effect of light intensity on photocatalysis was also conducted. The results show that photocatalytic oxidation is an effective method for phenol removal from waters. The degradation rate can be improved by applying an anodic bias to the TiO 2/Ti film electrode, phenol can not be decomposed under only 365 nm UV light irradiation even in the presence of hydrogen peroxide. In the range of our research, the phenol removal rate can be described in terms of pseudo first order kinetics.

TiO_2 photocatalytic antifungal technique for crops diseases control

TiO2 and 1% Ce^3＋-TiO2 prepared by hydrothermal method were characterized by means of XRD and UV-visible diffusive reflectance spectra（DRS）. The results of DRS analysis indicated that the 1% Ce^3＋-TiO2 catalyst had significant optical absorption in the visible region between 400-450 nm because electrons could be excited from the valence band of TiO2 or cerium oxides to Ce 4f level. To investigate the photocatalytic activity of different catalysts for crop fungal disease control, a series of Quine tests were carried out for cucumber powdery mildew and litchi downy blight control in home-made photocatalytic reactor. The results showed that TiO2 photocatalysis technique should be effective to inhibit the growth of fungal diseases to some extent and P-25 had a higher activity for antifungal control than home-made TiO2 catalysts. TiO2-A prepared with Ti（SO4）2 is more active to contro 1 antifungal disease than TiO2-B prepared with TiOSO4 as precursor because the crystalline of TiO2-A was higher than that of TiO2-B. The antifungal index litchi downy blight control was greatly enhanced by doping 1% cerium ion. The antifungal index of 1.0%Ce3^＋-TiO2 was（47.0 ± 4.7）%, （82.2 ± 3.5）%, （100 ±0.0）% under indoor weaker light, solar light and black light, respectively. The results of field experiments showed that the antifungal index of 1.0%Ce^3＋-TiO2 was more than that of P-25. The antifungal index of 1.0%Ce^3＋-TiO2 was （81.7 ± 6.5）%, （67.5 ±4.7）%, （38.6±1.9）% for litchi downy blight, maize southern leaf spot, and rice blast, respectively. It was concluded that TiO2 photocatalysis technique should be an effective way for litchi fungal disease control in practice.

Adsorption and photocatalytic degradation of phenol over TiO_2/ACF

The adsorption and photocatalytic degradation of phenol in water were investigated in a cylindrical borosilicon glass photoreactor with a cooling water jacket using TiO 2/ACF as photocatalyst. A 15 W UV lamp(254 nm) was used as central light source. The effects of the temperature and initial concentration of phenol solution on adsorption and photocatalytic process were studied, and the comparison of adsorption, photolysis and photocatalysis was conducted. The results show that the classical model of Langmuir gives a good description of the adsorption of phenol on TiO 2/ACF and low temperature can improve the adsorption of phenol on photocatalyst; increasing temperature can increase the photocatalytic degradation rate of phenol; and the adsorption enhances the photocatalytic removal of phenol.

Photocatalytic reaction kinetics model based on electrical double layer theory Ⅲ.Surface complexation model of methyl orange adsorption on TiO_2 surface

Based on the infrared characterization of methyl orange adsorption on TiO 2 surface and the titration of TiO 2, the triple layer model of methyl orange adsorption on TiO 2 was established according to electric double theory. The software FITEQL3.1 was applied to calculate the distribution of organic adsorption on TiO 2 surface by introducing dummy components to help to overcome mathematical difficulties. It is shown that the chem. adsorption species of methyl orange have a great adsorption amount. The adsorption constants of three kinds of surface complexation expressed as SOH +org -,SOH 2org 2 and SOHorg - are 5.98, 17.57 and -4.2, respectively.

Photocatalytic reaction kinetics model based on electrical double layer theoryⅡ. Infrared spectroscopic characterization of methyl orange adsorption on TiO_2 surface

In the process of heterogeneous photo catalytic degradation, the reaction rate depends strongly on the property of organic binding on the surface. It is important to identify the adsorption of organic compounds on TiO 2 surface to understand the mechanism of degradation and proper kinetics expression. The infrared spectroscopy was used to analyze the methyl orange adsorption on TiO 2 surface in aqueous solutions in different pH ranges. The variation of the surface complexation of methyl orange formed on the TiO 2 surface in different acid and basic media was discussed. And the adsorption amounts were also qualitatively analyzed. Methyl orange has strong, weak and little adsorption on the TiO 2 surface in acid, basic and near neutral solution, respectively.

Dependence of bisphenol A photodegradation on the initial concentration of oxalate in the lepidocrocite-oxalate complex system

To understand the degradation of endocrine disrupting chemicals （EDCs） in natural environment with existence of iron oxides and carboxylic acids, the dependence of bisphenol A （BPA） photodegradation on the initial concentration of oxalate （Cox） in lepidocrocite （y-FeOOH） aqueous suspension was investigated under both UV and visible lights in this study. Lepidocrocite powder was home-prepared by a hydrothermal process. It was found that BPA degradation was promoted greatly in the presence of oxalate owing to the formation of lepidocrocite-oxalate complex. And there was an optimal Cox, which was 2.0 and 2.4 mmol/L, under UV and visible lights, respectively. The first-order kinetic constant, k value increased 38 times from 0.17 × 10^-2 min^-1 in the absence of oxalate to 6.39 × 10^-2 min^-1 in the presence of oxalate with an optimal Cox （2.0 mmol/L） under UV irradiation, and almost 306 times from 0.02 × 10^-2 min^-1 in the absence of oxalate to 6.11 × 10^-2 min^-1 in the presence of oxalate with an optimal Cox （2.4 mmol/L） under visible irradiation. The BPA degradation rate increased and the first-order kinetic constants decreased with the increase in BPA initial concentration. The dependence of the variation of pH value, total-Fe and Fe^2＋ during the photoreaction on Cox was also investigated. The pH value increased obviously with the reaction time. Total-Fe increased dramatically at the first 5 min and then decreased quickly under UV irradiation and slowly under visible irradiation. The initial concentration of oxalate is a main factor to affect BPA photodegradation in aqueous suspension under both UV and visible lights.

Fractionation characteristics of rare earth elements(REEs) linked with secondary Fe, Mn, and Al minerals in soils

Soil secondary minerals are important scavengers of rare earth elements(REEs) in soils and thus affect geochemical behavior and occurrence of REEs. The fractionation of REEs is a common geochemical phenomenon in soils but has received little attention, especially fractionation induced by secondary minerals. In this study, REEs(La to Lu and Y) associated with soil-abundant secondary minerals Fe-, Al-, and Mn-oxides in 196 soil samples were investigated to explore the fractionation and anomalies of REEs related to the minerals. The results show right-inclined chondrite-normalized REE patterns for La–Lu in soils subjected to total soil digestion and partial soil extraction. Light REEs(LREEs) enrichment features were negatively correlated with a Eu anomaly and positively correlated with a Ce anomaly. The fractionation between LREEs and heavy REEs(HREEs) was attributed to the high adsorption affinity of LREEs to secondary minerals and the preferred activation/leaching of HREEs.The substantial fractions of REEs in soils extracted byoxalate and Dithionite-Citrate-Bicarbonate buffer solutions were labile(10 %–30 %), which were similar to the mass fraction of Fe(10 %–20 %). Furthermore, Eu was found to be more mobile than the other REEs in the soils, whereas Ce was less mobile. These results add to our understanding of the distribution and geochemical behavior of REEs in soils, and also help to deduce the conditions of soil formation from REE fractionation.

Effect of environmental C/N ratio on activities of lignin-degrading enzymes produced by Phanerochaete chrysosporium

Lignin-degrading enzymes secreted by white rot fungi play an important role in the degradation of lignin and persistent organic pollutants(POPs).In this study,effect of environmental C/N ratio on the activities of lignin-degrading enzymes,lignin peroxide(Li P)and manganese peroxidase(Mn P),produced by Phanerochaete chrysosporium,a white rot fungus,was investigated.Glucose was used as C source,and ammonium tartrate of different concentrations was used as N source to provide different C/N ratios.Relationships between Li P and Mn P activities and environmental C/N ratio were explored.The results showed that the higher the N source concentration,the faster the mycelium pellets aged.The faster the mycelium dry weight increased,the higher the Li P and Mn P activities.A high C/N ratio was a necessary condition for the secretion of Li P or Mn P.In addition,mycelium dry weight essentially affected enzyme activities.In the 122 C/N ratio and 50 C/N ratio treatments,mycelium dry weight essentially affected Mn P activity and both Li P and Mn P activities,respectively.

Interactively interfacial reaction of iron-reducing bacterium and goethite for reductive dechlorination of chlorinated organic compounds

The interactively interfacial reactions between the iron-reducing bacterium (Shewanella decolorationis, S12) and iron oxide (α-FeOOH) were investigated to determine reductive dechlorination transformation of chlorinated organic compounds (chloroform and pentachlorophenol). The results showed that the interactive system of S12+ α-FeOOH exhibited relatively high dechlorination rate. By comparison, the S12 biotic system alone had no obvious dechlorination, and the α-FeOOH abiotic system showed low dechlorination rate. The enhanced dechlorination of chloroform and pentachlorophenol in the interactive system of S12+α-FeOOH was derived from the promoted generation of adsorbed Fe(Ⅱ) by S12. A decrease in redox potential of the Fe(Ⅲ)/Fe(Ⅱ) couple in the interactive reaction system was determined by cyclic voltammetry. Our results will give new insight into interactively interfacial reaction between iron-reducing bacterium and iron oxides for degradation of chlorinated organic compounds under anaerobic condition.

Adsorption of 2-mercaptobenzothiazole from aqueous solution by organo-bentonite

The adsorption behavior of 2-mercaptobenzothiazole onto organo-bentonite was investigated. Natural bentonite from Gaozhou in Guangdong Province, China was collected. Organo-bentonite was prepared by intercalation of cetyltrimethyl ammonium bromide into the natural bentonite. The physicochemical properties of the prepared organo-bentonite were characterized by X-ray diffraction, N2 adsorption-desorption isotherm and Fourier transform infrared spectroscopy. The results showed that montmorillonite is the main component of the natural bentonite. The basal spacing of the natural bentonite is 1.47 nm, which increased to 1.98 nm on intercalation with cetyltrimethyl ammonium bromide. Moreover, both the surface area and pore volume increased with intercalation. Clear CH2 stretching （3000-2800 cm-1） and scissoring （1480-1450 cm-1） modes of the intercalated surfactants were observed for organo- bentonite. Compared with the pseudo first-order kinetic model, the pseudo second-order kinetic model is more suitable to describe the adsorption kinetics of 2-mercaptobenzothiazole onto organo-bentonite. The adsorption capacity of 2-mercaptobenzothiazole onto organo-bentonite increased with increasing initial concentration of 2-mercaptobenzothiazole, but decreased with increasing adsorbent dosage. The adsorption isotherm of 2-mercaptobenzothiazole onto organo-bentonite fits well with the Langmuir model. The maximum adsorption capacity of organo-bentonite for 2-mercaptobenzothiazole was 33.61 mg/g, indicating that organo-bentonite is a promising adsorbent for 2-mercaptobenzothiazole.

Influence factors for the oxidation of pyrite by oxygen and birnessite in aqueous systems

The oxidation of exposed pyrite causes acid mine drainage, soil acidification, and the release of toxic metal ions. As the important abiotic oxidants in supergene environments,oxygen and manganese oxides participate in the oxidation of pyrite. In this work, the oxidation processes of natural pyrite by oxygen and birnessite were studied in simulated systems, and the influence of p H, Fe（II） and Cr（III） on the intermediates and redox rate was investigated. SO42-and elemental S were formed as the major and minor products,respectively, during the oxidation processes. Ferric（hydr） oxides including Fe（OH）3and goethite were formed with low degree of crystallinity. Low p H and long-term reaction facilitated the formation of goethite and ferric hydroxide, respectively. The rate of pyrite oxidation by birnessite was enhanced in the presence of air（oxygen）, and Fe（II） ions played a key role in the redox process. The addition of Fe（II） ions to the reaction system significantly enhanced the oxidation rate of pyrite; however, the presence of Cr（III） ions remarkably decreased the pyrite oxidation rate in aqueous systems. The introduction of Fe（II） ions to form a Fe（III）/Fe（II） redox couple facilitated the electron transfer and accelerated the oxidation rate of pyrite. The present work suggests that isolation from air and decreasing the concentration of Fe（II） ions in aqueous solutions might be effective strategies to reduce the oxidation rate of pyrite in mining soils.

Reply to comments on “Adsorption of 2-mercaptobenzothiazole from aqueous solution by organo-bentonite” by Yuhshan Ho

There were several first-order kinetic equations used and cited by previous publications （Do,an et al., 2007; Eftekhari et al., 2010; Lagergren, 1898; Kannan and Sundaram, 2001;Ozcan et al., 2006）：