隐伏断裂的地气测量及其意义

传统概念的地气测量是指地下上升到地表并扩散到大气空间的天然状态气体 ,如CO2 、CH4 、Rn、Hg、H2 等。近十多年的研究证实地气还包含着新的内涵 ,即地壳岩石以及地表土壤中还存着痕量的金属与非金属气体 ,通过捕集这些气体 ,可以获得更多的深部地质构造、矿床信息。据报导 ,国内外的研究主要是在已知矿床上做的正演研究。本文是在已知隐伏断层构造上方地表 ,试验金属与非金属地气存在的可能性。     

生物过滤技术在大气污染控制中的应用

生物过滤是控制大气污染的经济有效技术,具有较好的发展前景。本文介绍了生物过滤技术处理废气的研究,应用历史,现状,和生物过滤理论,分析了工艺的使用范围,设计及运行控制要点,列举了应用的范例。     

Characterization of Organic Compounds in Compost-Amended Soil

Samples of compost-amended soil from waste dumping sites in Lagos Metropolis were extracted with dichloromethane (3 × 20 cm³) and the extract was evaporated at 35 °>C. The residue was extracted with 2,2,4-trimethylpentane, and portions of the solution were applied to a column containing silica gel from which aliphatic and aromatic hydrocarbons were eluted with n-hexane and toluene respectively. Analysis of the n-hexane fraction using gas chromatography showed the presence of a mixture of aliphatic hydrocarbons, ranging from C₉ to C₂₅, while ultraviolet analysis of the toluene fraction suggested 1,2-benzanthracene; 2,3-benzphenanthrene, chrysene and pyrene as polyaromatic compounds present in samples analyzed. The crude extracts were highly coloured and viscous. Total extractable organic residues in the 2,2,4-trimethylpentane extracts ranged from 36 to 89 mg g^-1 of soil.     

Heavy metal contamination in the vicinity of an industrial area near Bucharest

BACKGROUND, AIMS AND SCOPE: Chromium enters into the aquatic environment as a result of effluent discharge from steel works, electroplating, leather tanning industries and chemical industries. As the Cr(VI) is very harmful to living organisms, it should be quickly removed from the environment when it happens to be contaminated. Therefore, the aim of this laboratory research was to develop a rapid, simple and adaptable solvent extraction system to quantitatively remove Cr(VI) from polluted waters. METHODS: Aqueous salt-solutions containing Cr(VI) as CrO4(2-) at ppm level (4-6 ppm) were prepared. Equal volumes (5 ml) of aqueous and organic (2-PrOH) phases were mixed in a 10 ml centrifuge tube for 15 min, centrifuged and separated. Concentrations of Cr(VI), in both the aqueous and organic phases, were determined by atomic absorption spectrometry. The effects of salt and acid concentrations, and phase-contact time on the extraction of Cr(VI) were investigated. In addition, the extraction of Cr(VI) was assessed in the presence of tetramethylammonium chloride (TMAC) in 2-PrOH phase. Effects of some other metals, (Cd(II), Co(II), Cu(II), Ni(II) and Zn(II)), on the extraction of Cr(VI) were also investigated. RESULTS AND DISCUSSION: The Cr(VI) at ppm level was extracted quantitatively by salting-out the homogeneous system of water and 2-propanol(2-PrOH) using chloride salts, namely CaCl2 or NaCl, under acidic chloride media. The extracted chemical species of Cr(VI) was confirmed to be the CrO3Cl-. The ion-pair complex extracted into the organic phase was rationalized as the solvated ion-pair complex of [2-PrOH2+, CrO3Cl-]. The complex was no longer stable. It implied the reaction between extracted species. Studies revealed that salts and acid directly participated in the formation of the above complex. Use of extracting agents (TMAC) didn't show any significant effect on the extraction of Cr(VI) under high salting-out conditions. There is no significant interference effect on the extraction of Cr(VI) by the presence of other metals. The Cr(VI) in the organic phase was back-extracted using an aqueous ammonia solution (1.6 mol dm(-3)) containing 3 mol dm(-3) NaCl. The extraction mechanism of Cr(VI) is also discussed. CONCLUSIONS: Salting-out of homogeneous mixed solvent of 2-propanol can be employed to extract Cr(VI) quantitatively, as an ion-pair of [2-PrOH2+ * CrO3Cl-] solvated by 2-PrOH molecules. Then, the complex becomes 'solvent-like' and is readily separated into the organic phase. The increase of Cl- ion concentration in the aqueous phase favors the extraction. The 2-PrOH, salts and acid play important roles in the extraction process. There is no need to use an extracting agent at a high salting-out condition. RECOMMENDATIONS AND PERSPECTIVES: Chromium(VI) must be quickly removed before it enters into the natural cycle. As the 2-PrOH is water-miscible in any proportion, ion-pairing between 2-PrOH2+ and CrO3Cl- becomes very fast. As a result, Cr(VI) can easily be extracted. Therefore, the method is recommended as a simple, rapid and adaptable method to quickly separate Cr(VI) from aqueous samples.     

多器件联合L波段强电磁脉冲防护模块仿真设计

目的 设计针对L波段射频前端敏感器件的强电磁脉冲防护模块,利用瞬态电压抑制二极管、气体放电管和发夹型微带带通滤波器进行联合仿真设计。方法 瞬态电压抑制二极管具有快速响应时间,气体放电管具有高功率容量,而微带带通滤波器可分离噪声信号,并保留有效信号。通过结合这些器件进行防护设计,可以充分发挥各自优势,提高系统稳定性和强电磁脉冲防护能力。结果 该模块设计工作频段为1.3~ 1.7 GHz,带内插入损耗小于1.5 dB,在70 dBm功率注入的情况下,防护效果可以达到42.5 dB,具有良好的防护效果。结论 通过分析研究不同器件的特性和优化设计,实现了对L波段频谱的防护,具有重要的实用价值和广阔的应用前景。     

管道内瓦斯爆炸温度与压力峰值试验研究

为分析瓦斯爆炸的火焰温度及压力峰值在管道中的传播规律,采用瓦斯管网爆炸测试系统进行试验,通过爆炸压力和爆炸火焰温度采集系统采集数据。在相同点火能量和点火位置的条件下,分析了体积分数对瓦斯爆炸的温度峰值和压力峰值的影响,及温度峰值和压力峰值随管道距离的变化规律。结果表明:当瓦斯体积分数低于9.5%时,温度峰值和压力峰值随瓦斯体积分数增大而增大;同一体积分数下,温度峰值最大值出现在最接近爆源的位置,并呈逐渐下降的趋势,接近爆源的温度峰值下降较明显,随管道延长,温度峰值的下降减慢且趋于平缓;温度峰值与传播距离近似呈三次函数关系;冲击波压力峰值随管道传播呈先上升后下降再上升的波动性变化。     

生物膜填料塔净化有机废气研究

为在国内开展生物化学法净化低浓度有机废气的研究工作,采用国内现有微生物菌种挂膜接种的生物膜填料塔净化低浓度甲苯废气,结果表明,在入口气体甲苯浓度0.183～1.803mg/L及气体流量86.4～190.8L/h（停留时间6.2～13.6s）的实验范围内,增加入口气体甲苯浓度和气体流量,可使甲苯的生化去除量增大,每升体积的生物膜填料对甲苯的生化去除量最大可达157.13mg/h。由实验结果推断,生物膜填料塔对废气中甲苯的净化去除过程属于传质控制过程。对比结果表明,本研究建立的动力学模式对实际过程有很好的适用性,计算值与实验值之间的相关系数R＝0.98。     

生物法净化处理低浓度挥发性有机及恶臭气体

结合课题组研究工作,概要介绍生物法废气净化技术的基础菌种及应用条件、菌种库与菌种批量生产线、初步工业应用等方面的研究成果与应用情况。     

TiO2薄膜光催化效果的强化

采用溶胶-凝胶法制备TiO2溶胶,将其涂覆在普通钠钙玻璃上,以TiO2对甲基橙的光分解率探讨TiO2薄膜最佳光催化性能.结果表明,当PEG400的加入量为7%时,TiO2薄膜的光催化性能最强;用锐钛型TiO2粉末二次引发的溶胶提拉制成的薄膜对甲基橙的光催化分解效果有很大的提高;经滴加操作后薄膜的光催化性能有明显改善;各个影响因素最好的组合效果为滴加操作 锐钛型粉体引发 H2SO4超强酸化 La3 掺杂.     

气候政策研究中的数学模型评述

按照成本分析和综合分析2个层次，分别介绍了投入产出模型、可计算一般均衡模型、宏观计量经济模型、工程经济模型、动态能源优化模型、能源系统模拟模型、综合评估模型等不同模型方法的特点及其在气候政策分析中的应用。指出可计算一般均衡模型是应用得最为广泛的方法之一。概括了气候政策模型研究的4个发展趋势，包括加强综合评估模型的应用、扩展成本与效益的内涵、注重不同模型之间的比较、强调不确定性分析。结果中国研究现状，分析了当前面昨的问题，认为国内气候政策模型研究与中国在国际气候变化领域的地位仍不相称，强度要进一步加强研究队伍建设、扩展研究领域、跟踪国际研究前沿问题，以便为国家的气候谈判政策提供更有效的科学依据和决策支持。