三峡库区汛期极端降水非均匀性特征

利用极端降水量集中度和集中期讨论三峡库区汛期极端降水量的非均匀性分布特征。结果表明: 三峡库区极端降水量空间分布表现为西南部和东北部地区相对较少,中部、东南部相对较多。库区汛期极端降水集中度和集中期的空间差异不大,集中程度总体较差,东北部和西部地区极端降水相对集中,中部相对分散。库区极端降水主要集中在6月底和7月上中旬,东北部和西部偏西地区集中期相对较晚,中部地区集中期相对较早。库区汛期极端降水量的分配状况与同期极端降水量存在较好的关系,即极端降水量越少,则极端降水量越集中、集中期越早;反之极端降水量越多,则极端降水量越分散、集中期越晚,尤其是在库区东北部地区最为显著。三峡库区蓄水后极端降水集中程度在空间上一致性较好,表现为蓄水后更为分散;极端降水量和集中期则在空间上差异显著,大致表现为蓄水后东北部极端降水增加并延迟;西南部极端降水减少并提前     

焊点热疲劳失效原因分析

某PCBA样品在使用约半年后出现功能失效,该PCBA在封装后进行整体灌胶,将失效样品剥离,发现部分器件直接脱落,通过表面观察、切片分析、EBSD分析、应力分析、热膨胀系数测试等手段对样品进行分析,结果表明:各封装材料存在热失配,且焊点缺陷较多且存在应力集中区,加速焊点的疲劳失效进程,导致PCBA功能失效。     

An experimental apparatus for testing biodiesels based on a CFR engine—setup and validation with different methyl ester blends

A cooperative fuel research (CFR) engine was modified and instrumented in order to control operating conditions and to measure engine parameters and in-cylinder pressure diagrams. Aiming at the comparison of different alternative fuels, an experimental procedure was defined, including cetane number (CN) evaluation and the definition of engine operating quantities in different working points, for fixed levels of compression ratio (CR) and injection advance. An investigation was made considering several blends of methyl-esters of rapeseed oil (RME) and of a mix of vegetable oils (VOME) with conventional diesel oil. The defined experimental procedure was applied to assess CN, engine brake thermal efficiency (bte) and exhaust emissions. Results show that the biodiesel content has a positive influence on soot emissions, with strong reduction, while thermal efficiency and NO_X emissions are negatively affected, which can be justified taking into account fuel properties and changes in combustion process. As observed outcomes are generally in line with those presented in literature, the facility proved to be a suitable tool for basic investigations on alternative fuels to be used in specific applications.     

近50年鄱阳湖五大流域降水变化特征研究

基于鄱阳湖流域在江西省内部分对应的79县市气象站1960～2006年逐日降水观测资料,采用线性回归的方法分别研究五大流域的年降水量、降水日数、暴雨日数等3要素的变化趋势,并用Mann法进行了变化趋势的显著性检验,用距平与均方差之比达到15和20作为气候异常检验指标,对各流域的各时间序列进行了异常检验,采用了Mann Kendall法对各时间序列进行突变检测。结果表明：（1）各流域的年降水量变化趋势基本一致,年降水量与年暴雨日数密切相关;饶河流域强降水事件较多,降水强度大,赣江中游流域降水时间分布相对较均匀,强降水事件较少;（2）各流域年降水量、暴雨日数总体呈波动上升趋势,20世纪90年代以来暴雨日数异常偏多的概率最大;（3）年降水日数以20世纪80年代中期为界,之前呈波动上升趋势,之后呈波动下降趋势,2002年至今各流域降雨日数明显偏少;（4）各流域的年降水量、降水日数、暴雨日数均未出现趋势性的突变;（5）近50年来鄱阳湖流域降水时间分布不均的情况加剧,旱涝灾害风险增加。     

Oxidative properties of ambient PM2.5 and elemental composition: Heterogeneous associations in 19 European cities

We assessed the extent to which constituents of PM_2.5 (transition metals, sodium, chloride) contribute to the ability to generate hydroxyl radicals (OH) in vitro in PM_2.5 sampled at 20 locations in 19 European centres participating in the European Community Respiratory Health Survey. PM_2.5 samples (n = 716) were collected on filters over one year and the oxidative activity of particle suspensions obtained from these filters was then assessed by measuring their ability to generate OH in the presence of hydrogen peroxide. Associations between OH formation and the studied PM constituents were heterogeneous. The total explained variance ranged from 85% in Norwich to only 6% in Albacete. Among the 20 centres, 15 showed positive correlations between one or more of the measured transition metals (copper, iron, manganese, lead, vanadium and titanium) and OH formation. In 9 of 20 centres OH formation was negatively associated with chloride, and in 3 centres with sodium. Across 19 European cities, elements which explained the largest variations in OH formation were chloride, iron and sodium.     

降低循环冷却水水耗的生产措施

为了有效降低循环冷却水系统补充水量、排污量,节约水处理剂的消耗、降低冷却水处理成本,关键在于提高循环水的浓缩倍数。本文对影响循环水浓缩倍数的因素进行了分析,总结了哈尔滨石化公司循环水场存在的问题。同时本文给出了提高循环水浓缩倍数的方法,上述方法能取得显著的环境效益和经济效益。     

Short-term seasonal variability in Be wet deposition in a semiarid ecosystem of central Argentina

The ⁷Be wet deposition has been intensively investigated in a semiarid region at San Luis Province, Argentina. From November 2006 to May 2008, the ⁷Be content in rainwater was determined in 58 individual rain events, randomly comprising more than 50% of all individual precipitations at the sampling period. ⁷Be activity concentration in rainwater ranged from 0.7 ± 0.3 Bq l⁻¹ to 3.2 ± 0.7 Bq l⁻¹, with a mean value of 1.7 Bq l⁻¹ (sd = 0.53 Bq l⁻¹). No relationship was found between ⁷Be content in rainwater and (a) rainfall amount, (b) precipitation intensity and (c) elapsed time between events. ⁷Be ground deposition was found to be well correlated with rainfall amount (R = 0.92). For the precipitation events considered, the ⁷Be depositional fluxes ranged from 1.1 to 120 Bq m⁻², with a mean value of 32.7 Bq m⁻² (sd = 29.9 Bq m⁻²). The annual depositional flux was estimated at 1140 ± 120 Bq m⁻² y⁻¹. Assuming the same monthly deposition pattern and that the ⁷Be content in soil decreases only through radioactive decay, the seasonal variation of ⁷Be areal activity density in soil was estimated. Results of this investigation may contribute to a valuable characterization of ⁷Be input in the explored semiarid ecosystem and its potential use as tracer of environmental processes.     

Gas/particle partitioning of atmospheric PCDD/Fs in a satellite town in Eastern China

Gas/particle partitioning of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in ambient air was investigated in a satellite town in Eastern China from April 2007 to January 2008 comprehending large temperature variations (from 3 to 34 °C, daily average). Molecular weight, molecular structure and ambient temperatures are the three major factors that govern the gas/particle partitioning of atmospheric PCDD/Fs throughout the year. Generally, good agreements were obtained (except for winter) between measured particulate fractions and theoretical estimates of both the Junge–Pankow adsorption model and Harner Bidleman absorption model using different sets of subcooled liquid vapor pressure and octanol–air partition coefficient (K_oa), respectively. Models utilizing estimates, derived from gas chromatographic retention indices (GC-RIs), are more accurate than that of entropy-based. Moreover, during winter, the K_oa-based model using the GC-RIs approach performs better on lower chlorinated PCDD/Fs than that of -based. Furthermore, possible sources of mismatch between measured and predicted values in winter (3–7 °C) were discussed. Gas adsorption artifact was demonstrated to be of minor importance for the phenomena observed. On the other hand, large deviations of slopes (m_r) and intercepts (b_r) in logK_p vs. plots from theoretical values are observed in the literature data and these are found to be linearly correlated with ambient temperatures (P<0.001) in this study. This indicates that the non-equilibrium partitioning of PCDD/Fs in winter may be significantly influenced by the colder temperatures that may have slowed down the exchange between gaseous and particulate fractions.     

The effect of alkyl chain length on the degradation of alkylimidazolium- and pyridinium-type ionic liquids in a Fenton-like system

Background, aim, and scope  Ionic liquids are regarded as essentially “green” chemicals because of their insignificant vapor pressure and, hence, are a good alternative to the emissions of toxic conventional volatile solvents. Not only because of their attractive industrial applications, but also due to their very high stability, ionic liquids could soon become persistent contaminants of technological wastewaters and, moreover, break through into natural waters following classical treatment systems. The removal of harmful organic pollutants has forced the development of new methodologies known as advanced oxidation processes (AOPs). Among them, the Fenton and Fenton-like reactions are usually modified by the use of a higher hydrogen peroxide concentration and through different catalysts. The aim of this study was to assess the effect of hydrogen peroxide concentration on degradation rates in a Fenton-like system of alkylimidazolium ionic liquids with alkyl chains of varying length and 3-methyl-N-butylpyridinium chloride. Materials and methods  The ionic liquids were oxidized in dilute aqueous solution in the presence of two different concentrations of hydrogen peroxide. All reactions were performed in the dark to prevent photoreduction of Fe(III). The concentrations of ionic liquids during the process were monitored with high-performance liquid chromatography. Preliminary degradation pathways were studied with the aid of ¹H NMR. Results  Degradation of ionic liquids in this system was quite effective. Increasing the H₂O₂ concentration from 100 to 400 mM improved ionic liquid degradation from 57–84% to 87–100% after 60 min reaction time. Resistance to degradation was weaker, the shorter the alkyl chain. Discussion  The compound omimCl was more resistant to oxidation then other compounds, which suggests that the oxidation rates of imidazolium ionic liquids by OH· are structure-dependent and are correlated with the n-alkyl chain length substituted at the N-1-position. The level of degradation was dependent on the type of head group. Replacing the imidazolium head group with pyridinium increased resistance to degradation. Nonetheless, lengthening the alkyl chain from four to eight carbons lowered the rate of ionic liquid degradation to a greater extent than changing the head group from imidazolium to pyridinium. 1H-NMR spectra show, in the first stage of degradation, that it is likely that radical attack is nonspecific, with any one of the carbon atoms in the ring and the n-alkyl chain being susceptible to attack. Conclusions  The proposed method has proven to be an efficient and reliable method for the degradation of imidazolium ionic liquids by a Fenton-like reagent deteriorated with lengthening n-alkyl substituents and by replacing the imidazolium head group with pyridinium. The enhanced resistance of 1-butyl-3-methylpyridinium chloride when the resistance of imidazolium ionic liquids decreases with increasing H₂O₂ concentration is probably indicative of a change in the degradation mechanism in a vigorous Fenton-like system. H-NMR spectra showed, in the first stage of degradation, that radical attack is nonspecific, with any one of the carbon atoms in the ring and the n-alkyl chain being susceptible to attack. Recommendations and perspectives  Since ionic liquids are now one of the most promising alternative chemicals of the future, the degradation and waste management studies should be integrated into a general development research of these chemicals. In the case of imidazolium and pyridinium ionic liquids that are known to be resistant to bio- or thermal degradation, studies in the field of AOPs should assist the future structural design as well as tailor the technological process of these chemicals     

Profile of Methane Concentrations in Soil and Atmosphere in Alpine Steppe Ecosystem on Tibetan Plateau

The methane concentration profile from -1.5m depth in soil to 32m height in air was measured in alpine steppe located in the permafrost area. Methane concentrations showed widely variations both in air and in soil during the study period. The mean concentrations in atmosphere were all higher than those in soil, and the highest methane concentration was found in air at the height of 16m with the lowest concentration occurring at the depth of 1.5m in soil. The variations of atmospheric methane concentrations did not show any clear pattern both temporally and spatially, although they exhibited a more steadystable state than those in soil. During the seasonal variations, the methane concentrations at different depths in soil were significantly correlated （R^2〉0.6） with each other comparing to the weak correlations （R^2〈0.2） between the atmospheric concentra- tions at different heights. Mean methane concentrations in soil significantly decreased with depth. This was the compositive influence of the decreasing production rates and the increasing methane oxidation rates, which was caused by the descent soil moisture with depth. Although the methane concentrations at all depths varied widely during the growing season, they showed very distinct temporal variations in the non-growing season. It was indicated from the literatures that methane oxidation rates were positively correlated with soil temperature. The higher methane concentrations in soil during the winter were determined by the lower methane oxidation rates with decreasing soil temperatures, whereas methane production rates had no reaction to the lower temperature. Relations between methane contribution and other environmental factors were not discussed in this paper for lacking of data, which impulse us to carry out further and more detailed studies in this unique area.