Hydrolysis kinetics of atrazine and influence factors

ＩｎｔｒｏｄｕｃｔｉｏｎＨｙｄｒｏｌｙｓｉｓｉｓｔｈｅｒｅａｃｔｉｏｎｏｆｃｈｅｍｉｃａｌｓｗｉｔｈｗａｔｅｒａｎｄａｌｓｏａｎｉｍｐｏｒｔａｎｔｅｎｖｉｒｏｎｍｅｎｔａｌｐｒｏｃｅｓｓｏｆｏｒｇａｎｉｃｐｏｌｌｕｔａｎｔｓ.Ｈｙｄｒｏｌｙｓｉｓｏｆｓｙｎｔｈｅｔｉｃｏｒｇａｎｉｃｃｏｍｐｏｕｎｄｓｏｃｃｕｒｓｖｉａｓｅｖｅｒａｌｐａｔｈｗａｙｓｗｈｉｃｈｉｎｖｏｌｖｅｔｈｅｓｐｅｃｉｆｉｃ ａｃｉｄ , ｂａｓｅａｎｄｎｅｕｔｒａｌｐｒｏｃｅｓｓｅｓ.Ｉｎａｄｄｉｔｉｏｎ ,ｗａｔｅｒｄｉｓｓｏｃｉａ…     

气候波动与土地利用变化对西班牙比利牛斯山脉中部径流影响的评价

在地中海国家扩大灌溉土地的面积,应当考虑气候与土地利用变化对水资源的影响.本文利用降水和温度资料,分析了20世纪中叶以来西班牙比利牛斯山脉中部流域径流的变化趋势.降水与径流之间关系的年变化表明,径流在所研究期间的后半时段相对较低,这一趋势与土地利用变化一致.在月水平上,降水量在10月、4月和7月明显增加,而在3月则有下降;温度在1月和2月有所增加,而在4月则趋于下降.但过去50年间径流在大部分月份中呈显著下降趋势,土地利用和植被覆盖的变化是解释年平均径流下降大约30%的惟一非气候因素.     

Environmental change in Bashang region historical periods

ＩｎｔｒｏｄｕｃｔｉｏｎＴｈｅＢａｓｈａｎｇｒｅｇｉｏｎｉｓｓｉｔｕａｔｅｄａｔｅａｓｔｌｏｎｇｉｔｕｄｅ113°50′-118°00′ａｎｄｎｏｒｔｈｌａｔｉｔｕｄｅ40°58′-42°42′,ｗｉｔｈａｎａｒｅａｏｆ17371ｋｍ2ｆｒｏｍＺｈａｎｇｊｉａｋｏｕｏｆｎｏｒｔｈｅｒｎＨｅｂｅｉｔｏｔｈｅｎｏｒｔｈｏｆＣｈｅｎｇｄｅ.ＴｈｅｒｅｇｉｏｎｌｉｅｓｉｎｔｈｅｍｉｄｄｌｅｓｅｃｔｉｏｎｏｆａｔｒａｎｓｉｔｉｏｎｚｏｎｅｆｒｏｍａｇｒｉｃｕｌｔｕｒａｌｔｏｐａｓｔｏｒａｌｒｅｇｉｏｎｓｏｆｎｏｒｔｈｅｒｎＣｈｉｎａ…     

The enhancement of photodegradation efficiency using Pt–TiO2 catalyst

This study investigates the mechanism of photosensitization and the recombination of excited electron–hole pairs affected by depositing platinum (Pt) on the surface of titanium dioxide (TiO₂). A new catalyst of Pt–TiO₂ was prepared by a photoreduction process. Being model reactions, the photocatalytic oxidation of methylene blue (MB) and methyl orange (MO) in aqueous solutions using the Pt–TiO₂ catalyst was carried out under either UV or visible light irradiation. The experimental results indicate that an optimal content of 0.75%Pt–TiO₂ achieves the best photocatalytic performance of MB and MO degradation and that the Pt–TiO₂ catalyst can be sensitized by visible light. The interaction of Pt and TiO₂ was investigated by means of UV–Vis absorption spectra, photoluminescence emission spectra, and X-ray photoelectron emission spectroscopy. The Pt⁰, Pt²⁺ and Pt⁴⁺ species existing on the surface of Pt–TiO₂, and the Ti³⁺ species existing in its lattice may form a defect energy level. The Pt impurities, including Pt, Pt(OH)₂, and PtO₂, and the defect energy level absorb visible light more efficiently in comparison with the pure TiO₂ and hinder the recombination rate of excited electron–hole pairs.     

Variations in the emissions of volatile organic compounds from the toner for a specific photocopier

A laboratory thermal desorption apparatus was used to measure emissions from a number of nominally identical photocopier toners--manufactured to meet the specifications of one specific model copier--when these toners were heated to fuser temperature (180-200 degrees C). The objective was to assess how potential volatile organic compound (VOC) emissions from the toner for a given copier can vary, depending upon the production run and the supplier. Tests were performed on a series of toner (and associated raw polymer feedstock) samples obtained directly from a toner manufacturer, representing two production runs using a nonvented extrusion process, and on toner cartridges purchased from two local retailers, representing three different production lots (histories unknown). The results showed that the retailer toners consistently had up to 350% higher emissions of some major compounds (expressed as microgram of compound emitted/g of toner), and up to 100% lower emissions of others, relative to the manufacturer toners (p < or = 0.01). The manufacturer toners from one production run had emissions of certain compounds, and of total VOCs, that were modestly higher (13-18%) than those from the other run (p < or = 0.01). The emission differences between the retailer and manufacturer toners are probably due to differences in the manufacturing processes and/or feedstocks used to produce the toners from these different sources.     

A study of the particulate matter PM10 composition in the atmosphere of Chillán, Chile

Inhalable particulate matter (PM10) concentrations were measured over 24-h intervals at six different urban sites in the city of Chillán from September 2001 to April 2003. Sampling locations were selected to represent central city, commercial, residential, and industrial portions of the city. Chemical composition of PM10 was performed to samples of 47 mm diameter Teflon membranes within the city of Chillán. The spatial and temporal variability of the chemical composition of PM10 was evaluated taking into account additional data from meteorology and further air pollutants. The majority of PM mass was comprised of carbon, nitrate, sulfate, ammonium, and crustal components but in different proportion on different days and at different sites. The chemical analyses showed that carbonaceous substances and crustal material were the most abundant component of PM10 during the winter and summer, respectively. The concentrations of PM10 were higher during the cold season than during the warm season. The PM10 concentrations were higher in the downtown area of the city of Chillán, where also the chemical composition was more variable due to urban traffic and other anthropogenic sources.     

Role of amination of a polymeric adsorbent on phenol adsorption from aqueous solution

Adsorption of seven phenols, one aromatic carboxylic acid and one sulfonated aromatic acid from aqueous solution, by a hypercrosslinked polymeric adsorbent (CHA-111) and the derivative animated by dimethylamine was compared. The results of different adsorption isotherms indicated that amino group on the polymeric matrix played a significant role on adsorption of almost all the employed compounds. For most employed compounds adsorption capacities increase to different degree and significantly for those with lower value of pK(a). It may be attributed to the enhanced adsorbent-adsorbate interaction for amino group introduced on the polymeric matrix. The empirical Freundlich isotherm equation was employed to interpret the adsorbent-adsorbate interaction. The adsorption enthalpy change indicated the uptake of phenols on MCH-111 to be an enhanced physical adsorption because of the hydrogen-bonding interaction. Adsorption kinetic study of phenols on CHA-111 and MCH-111 was also conducted and amino group on the matrix will reduce the adsorption rate for change of pore size distribution and loss of macroprous volume as well as the hydration effect on the surface partly.     

Movement of bromacil and hexazinone in soils of Hawaiian pineapple fields

Bromacil and hexazinone have been heavily used to control weeds in the pineapple fields in central Oahu, Hawaii, USA, since 1970s and 1980s, respectively. The last application prior to this study was at a rate of 0.6 kg active ingredient (a.i.) ha(-1) for hexazinone and 1.8 or 3.4 kg (a.i.) ha(-1) for bromacil in the six study fields during June-October 1998. Soils were collected from 0 to 1860 cm below the surface in January-May 1999 to survey the residue profiles of the two herbicides. Stratoprobe sampling showed to be an efficient and convenient method for deep soil cores. Bromacil was detected in all the soil samples above 60 cm (105-1338 ng g(-1) dry weight) and in 74% of the samples above 400 cm (26-473 ng g(-1)). Trace amounts of bromacil (90-113 ng g(-1)) were detected in some of the samples collected from as deep as 1540 cm. Hexazinone was detected in three of the six fields at 0-60 cm only (86-107 ng g(-1) dry weight). The more frequent detection of bromacil at higher concentrations than hexazinone is related to the prolonged higher application rates of bromacil in the fields and its higher persistence and mobility in soil.     

Changes in soil solution Zn and pH and uptake of Zn by arbuscular mycorrhizal red clover in Zn-contaminated soil

Red clover plants inoculated with Glomus mosseae were grown in a sterile pasture soil containing 50 mg Zn kg(-1) in 'Plexiglas' (acrylic) containers with nylon net partitions (30 microm mesh) designed to separate the soil into a central root zone and two outer zones for hyphal growth with no root penetration. Two porous plastic soil moisture samplers were installed in each pot, one in the root compartment and the other in one of the hyphal compartments. The soil in the outer compartments was amended with one of the four application rates of Zn (as ZnSO4) ranging from 0 to 1000 mg kg(-1). Non-mycorrhizal controls were included, and there were five replicates of each treatment in a randomised block in a glasshouse. Uninoculated plants received supplementary P to avoid yield limitation due to low soil P status. Plants grew in the central compartment for nine weeks. Soil moisture samples were collected 4, 24 and 62 days after sowing to monitor changes in the Zn concentration and pH of the soil solution. At harvest, the mean mycorrhizal infection rate of inoculated plants ranged from 29% to 34% of total root length and was little affected by Zn application. Root and shoot yields were not affected by mycorrhizal infection. Plant Zn concentration and uptake were lower in mycorrhizal plants than non-mycorrhizal controls, and this effect was more pronounced with increasing Zn application rate to the soil. Soil solution Zn concentrations were lower and pH values were higher in mycorrhizal treatments than non-mycorrhizal controls and the mycorrhiza effect was more pronounced at higher Zn application rates. The protective effect of mycorrhiza against plant Zn uptake may have been associated with changes in Zn solubility mediated by changes in the soil solution pH, or by immobilisation of Zn in the extraradical mycelium.     

Effect of backyard burning on dioxin deposition and air concentrations

The influence from open burning of garden and household waste on locally measured dioxin deposition and air concentrations was evaluated in three sets of experiments: the combustion of garden waste in barrels and in open fires, and the incineration of household waste in an empty oil drum. Each set was composed of eight individual experiments over 4 h. Deposition gauges were located 20 m NE, SE, SW and NW with respect to the source and on a background location at 400 m SW. Air samples were taken in the plume with a medium volume sampler equipped with a quartz filter and a polyurethane plug. The results illustrate deposition increments in the wind direction at a distance of 20 m from the source of 0.8 pg TEQ/m2 day for garden waste and 2.5 pg TEQ/m2 day for household waste. Concentrations in the plume were increased by 160-580 fg TEQ/m3 over a period of 12 and 31 h respectively. Expressed at a reference CO2 concentration of 9% this corresponds with a range from 0.8 to 3.6 ng TEQ/m3, which is comparable with a poorly controlled MSWI. Emission factors in the order of magnitude of 4.5 ng TEQ/kg combusted garden waste and 35 ng TEQ/kg burned municipal waste were determined.