CuCl2蚀刻液制备CuCl的研究

以氯化钢蚀刻液废液、粗铜粉等为原料,在常温下反应制备氯化亚铜,工艺简便,产品质量好,具有显著的经济效益和环境效益。     

Atmospheric methyl chloride

There are about 5 Tg of methyl chloride in the Earth’s atmosphere making it one of the largest reservoirs of gas-phase chlorine. We discuss the time series of global measurements taken over the last 16 yr at seven locations distributed among the polar, middle, and tropical latitudes of both hemispheres (1981–1997). Measurements were also taken at 20 more sites between 1987 and 1989. The vertical distribution was measured during campaign experiments in the Arctic, Western Atlantic, and over Brazil. Small, mostly decreasing trends are observed, showing that on average, there was 4% less methyl chloride during the last three years (1994–1996) than there was in the first three years (1985–1987) of the experiment. The latitudinal variation is marked by highest concentrations in the tropics and lowest in the polar regions. Sites representing inland locations show higher concentrations, suggesting continental sources, mostly confined to the tropics. There are seasonal variations at various latitudes that can be explained mostly by the cycles of OH radicals, which are the dominant removal process for methyl chloride in the atmosphere. Based on these data, the expected emissions can be calculated at the polar, middle, and tropical latitudes represented by the six long-term primary sites. Using a photochemical model of OH, we estimate that a global source of about 3.7 Tg yr^-1 of methyl chloride is needed to explain the observed concentrations. Other removal processes have been identified that may add to this estimate of the global annual emissions. The results further establish that some 85% of the emissions must come from the half of the earth’s surface between 30°S and 30°N, representing tropical and sub-tropical latitudes. Small emissions are estimated for the middle latitudes, and no emissions are expected from the polar regions.     

An episode of dioxin contamination in feedingstuff: the choline chloride case

In 2000, as part of a survey programme, the German authorities detected high levels of dioxins in a choline chloride (CC) premix used as animal food component. The contaminated additive consisted of different products of mineral and vegetable origin acting as a carrier. The CC was manufactured in Belgium. The final product was produced in and distributed from a plant in Spain. The German authorities informed all European Community members of the incident. The Spanish Ministry of Agriculture, Fisheries and Food and the Regional Authorities immediately conducted a survey in collaboration with the Spanish Council for Scientific Research (CSIC) to determine and isolate the source of the contamination. Analysis of a large number of samples of pure CC, pine sawdust, almond shell and other substances currently used in the preparation of the premix confirmed the presence of a significant amount of polychlorinated dibenzo-p-dioxins/polychlorinated dibenzofurans in mixtures in which pine sawdust was present. An analysis of the congener profiles revealed similarities with those found in technical pentachlorophenol (PCP) formulations. The conclusion was that PCP-contaminated sawdust as carrier for CC was source of dioxin contamination in feedingstuff.     

Diffusion mechanism of chloride ions in sodium montmorillonite

For safety assessment of geological disposal of HLW, it is necessary to understand the diffusion mechanism of radionuclides in compacted bentonite. In this study, the diffusion behavior of chloride ions in compacted montmorillonite was studied from the viewpoints of the activation energy for apparent diffusion and the basal spacing of the compacted montmorillonite. A unique change in the activation energy as a function of the dry density of the montmorillonite was found. The activation energy decreased from 17.4 to 13.5 kJ mol-1 as the dry density increased from 0.7 to 1.0 Mg m-3 and increased to 25.1 kJ mol-1 at dry densities above 1.0 Mg m-3. The basal spacing of 1.88 nm, corresponding to the three-water layer hydrate state, was not observed by X-ray diffraction (XRD) until the dry density increased to 1.0 Mg m-3, where the minimum activation energy was obtained. On the other hand, a basal spacing of 1.56 nm, corresponding to the two-water layer hydrate state, was observed at the dry densities of 1.4 Mg m-3 and above, where the activation energies were more than 22 kJ mol-1. These experimental results suggest that there are at least two additional diffusion processes that can raise or reduce the activation energy and are affected by water in the region adjacent to the montmorillonite surfaces. If the "Grahame model" can be introduced to describe the electrical double layer, surface diffusion will be considered the possible predominant diffusion process, even for anions like chloride ions.     

聚合氯化铝铁的电动性能研究

通过测定Zeta电位对聚合氯化铝铁(PAFC)水解产物的电动特性进行了研究.通过对模拟悬浊水样的絮凝实验对PAFC除浊性能进行了考察.结果表明:PAFC水解产物的电动特性与pH,PAFC投加量和Al/Fe摩尔比的变化密切相关;PAFC是通过电中和、吸附架桥和卷扫作用起混凝作用的,3种作用的综合能力越强,其混凝效果就越好.     

Cadmium availability to the cyanobacterium Synechocystis aquatilis in solutions containing chloride

Availability of cadmium to Synechocystis aquatilis (estimated by 109Cd sorption and cadmium toxicity-14C method) in solutions containing cadmium and complexing (KCl) or non-complexing (KNO3) salts, in the range of 0-0.5 m was investigated. Both cadmium surface adsorption and transport into the cells were lower in solutions containing cadmium chloride complexes (CdCl+, CdCl2, CdCl3-) than in those containing cadmium in the form of Cd2+. Also, cadmium toxicity in solutions of higher KCl concentrations, in which CdCl+ and CdCl2 forms predominated, was significantly limited.     

Characterization of emissions of dioxins and furans from ethylene dichloride, vinyl chloride monomer and polyvinyl chloride facilities in the United States. Consolidated report

This is the consolidated report of emissions of PCDD/F from facilities in the organic chemical manufacturing chain leading to polyvinyl chloride. Data have been gathered from facilities in the US and Canada from a number of manufacturers and at various steps in the manufacturing process. Estimates of US emissions or transfers of PCDD/F were generated on an "Upper Bound" and "Most Likely" basis. The Most Likely estimate of US emissions of PCDD/F to the open environment, that is, air, water and land surface by facilities in this chain, based on evaluation of non-detects at one-half the detection limit is about 12 g I-TEQ per year. On this same basis, an estimated 19 g is disposed of in secure landfills.     

Formation of PCDDs and PCDFs during the combustion of polyvinylidene chloride

In laboratory-scale combustion of polyvinylidene chloride (PVDC) with a quartz tubular furnace designed and fabricated to provide the desired combustion temperature and mixing state of combustion gas with air, it was found that at 800 degrees C or higher the level of polychlorinated dibenzo-p-dioxins/polychlorinated dibenzofurans [corrected] (PCDDs/PCDFs) resulting from PVDC combustion was no higher than that from heating air alone, and thus far below the levels which resulted from PVDC combustion at 750 degrees C or lower. The results provide the first laboratory confirmation of the relation between PVDC incineration temperature and PCDD/PCDF formation, and of the primary importance of high temperature, turbulence for mixing between air and combustion gas, and sufficient residence time, as governing factors for the minimization of PCDD/PCDF formation in municipal solid waste incinerators.     

Methyl chloride emissions from halophyte leaf litter: dependence on temperature and chloride content

Methyl chloride (CH₃Cl) is the most abundant natural chlorine containing compound in the atmosphere, and responsible for a significant fraction of stratospheric ozone destruction. Understanding the global CH₃Cl budget is therefore of great importance. However, the strength of the individual sources and sinks is still uncertain. Leaf litter is a potentially important source of methyl chloride, but factors controlling the emissions are unclear. This study investigated CH₃Cl emissions from leaf litter of twelve halophyte species. The emissions were not due to biological activity, and emission rates varied between halophyte species up to two orders of magnitude. For all species, the CH₃Cl emission rates increased with temperature following the Arrhenius relation. Activation energies were similar for all investigated plant species, indicating that even though emissions vary largely between plant species, their response to changing temperatures is similar. The chloride and methoxyl group contents of the leaf litter samples were determined, but those parameters were not significantly correlated to the CH₃Cl emission rate.     

The role of copper(II) chloride in the formation of organic chlorine in fly ash

In the de-novo synthesis and formation of PCDD/PCDF, the transfer of inorganic chlorine to the carbonaceous material of fly ash plays an important role. Here, copper acts as a catalyst in the chlorination reaction. In experiments in the range of 250-350 degrees C under helium, we determined the stoichiometry of the chlorination reaction with model systems. Therefore, it was necessary to develop a method to quantify the copper(II) and copper(I) ions. In a combination of solid electron paramagnetic (spin) resonance spectroscopy (EPR) for Cu(I), and X-ray fluorescence spectroscopy (XRFA) analysis for Cu (total), we found a way for the quantification of copper(I) and (II). With these experiments, we can show that the chlorination reaction is relatively fast and comes to a stop under helium, after the copper(II) is reduced. The ratio between the organic chlorine formed and copper(II) reduced is, at the end of the reaction, 0.5, which is in agreement with the following reaction: 2CuCl2 + R-H-->2CuCl + R-Cl + HCl.     

Modelling methane and vinyl chloride in soil surrounding landfills

Sanitary landfilling is used in many countries as a preferred method for disposal of household wastes for reasons of simplicity and economics. Immediately following its deposition within a landfill, most of the organic fraction of waste will begin to undergo degradation through chemical and bacterial action. Landfill gas (LFG) is a product of biodegradation and consists of primarily methane (explosive) and carbon dioxide, with trace amounts of other volatiles that are often toxic gases (for example, vinyl chloride). LFG can migrate through the soil away from the landfill site and appear at the surface away from where it started. Since methane presents a fire or explosive threat, LFG must be controlled to protect property and public safety. To aid this, consideration must be given to models. Therefore, this study was undertaken to develop a simple numerical model by using a finite difference method in order to predict gas migration through the soil surrounding the landfill. The model construction was described as well as the landfill and its surrounding soil. The model was applied to predict methane and vinyl chloride concentrations at different distances from the landfill. Comparison between the predicted and measured values was calculated to evaluate the validity of the model. The agreement between measured and predicted concentrations was found, and this agreement is sufficiently good     

Natural attenuation in marine sediments: investigation of the effect of chloride concentration on the mobility of metals

Environmental Science and Pollution Research - Metals can be mobilized from contaminated sediments under variable environmental conditions. This paper discusses the effects of specific ions of the...     

Influence of metal ion on sorption of p-nitrophenol onto sediment in the presence of cetylpyridinium chloride

Heavy metals and surfactants have a significant effect on the sorption of organic contaminants. In this study, batch equilibrium experiments were carried out to investigate the influence of Pb(NO(3))(2) on the sorption of p-nitrophenol (PNP) onto sediments in the presence of cationic surfactant cetylpyridinium chloride (CPC). Results indicated that in the complex system containing PNP, Pb(NO(3))(2) and CPC, the sorption of PNP decreased with increasing concentration of Pb(NO(3))(2) due primarily to competing for adsorption sites. Likewise, partitioning of PNP in adsorbed surfactant layers and micelles decreased with increasing level of Pb(NO(3))(2). Moreover, the influence of different metal ions (Pb(2+), Cd(2+), Zn(2+)) was examined and results indicated that the presence of heavy metals inhibited the sorption of PNP in the order: Pb(2+)>Cd(2+)>Zn(2+). The competitive effect of the heavy metals was in agreement with the hydration energy and hydrated radius. The results are believed to provide a useful insight into describing the transport and fate of PNP in natural environments.     

Reduced cadmium accumulation in tobacco by sodium chloride priming

Environmental Science and Pollution Research - Cadmium (Cd) pollution threatens agricultural security worldwide. This study tested the efficacy of priming chemicals to decrease Cd uptake by tobacco...     

The effect of sodium chloride on the two-step kinetics of the nitrifying process.

Sodium chloride affects the transformation rate of several compounds in bioreactors. Most authors report a decrease in microorganism activity at increasing salt concentrations. In this work, a kinetic model that relates sodium chloride concentration with the rates of each step of the nitrification process is proposed; thus, the effect of sodium chloride concentration (0 to 60 g/L) on the nitritation and nitratation rates was separately studied. To carry out the independent study of each step, a combination of the respirometric method with sodium azide, an inhibitor of the nitratation step, was performed. The dot-blot hybridization technique with 16S rRNA-targeted probes was used to determine the ammonia-oxidizing and nitrite-oxidizing bacterial fraction, then it was possible to relate the culture's function with its biological composition. Rates of both steps were linearly reduced at increasing salt concentrations: the nitratation rate was more affected than the nitritation rate. Simulations carried out in a nitrifying sequencing batch reactor indicate that nitrite might accumulate at high salt concentrations. Sodium chloride exerts a reversible inhibition on ammonia oxidation and nitrite oxidation.     

聚合氯化铝铁去除微污染水体中藻类的研究

以聚合氯化铝铁(PAFC)为絮凝剂,H2O2为预氧化剂,用正交实验研究了PAFC处理微污染水体中藻类和降低浊度,得出正交实验中各因素的主次关系及对除藻和除浊度的影响,研究表明,ρPAFC是影响除藻和除浊度的重要因素.在最佳处理条件,即ρPAFC为20 mg/L,ρH2O2为6 mg/L,pH为7,搅拌时间为4 min,能使水体中藻细胞街度从9.4×107 cells/L降至3.16×106 cells/L,除藻率为96.6%,浊度降至0.70 NTU,除浊度率达93.0%.