几种药物治疗对虾聚缩虫病试验

本文报道了1990年在平湖对虾养殖场用几种药物治疗聚缩虫病所做的试验。结果表明,高锰酸钾和新洁尔灭的疗效较为显著。     

中国大陆科学钻探主孔超高压榴辉岩中绿辉石结构水研究

本文利用傅立叶（Fourier）变换红外光谱技术对CCSD主孔100～3100米深度范围榴辉岩中的绿辉石结构水含量进行了原位分析。结果表明，所有绿辉石都舍有一定的以OH形式存在的结构水，其含量范围为45～784ppm，平均为235ppm。不同榴辉岩绿辉石之间的结构水含量差别较大，而且呈现出明显的空间分布不均一性。相关性分析显示，绿辉石的结构水含量与全岩的Mgo、TFeO、Al2O3，含量成正相关，与NaO成反相关，与绿辉石的NaO、TFeO含量成负相关，与榴辉岩的峰期变质条件无关；与其它类型榴辉岩相比，多硅白云母榴辉岩中绿辉石的结构水含量较高，平均为339ppm。由此推测，超高压榴辉岩绿辉石中所残留的结构水含量很可能与其峰期结构水含量、矿物化学成分和岩石矿物组成有关。     

Performance of A Combination Process of UV/H2O2/Micro‐Aeration for Oxidation of Dichloroacetic Acid in Drinking Water

The decomposition of dichloroacetic acid (DCAA) in water using a UV/H₂O₂/micro‐aeration process was investigated in this paper. DCAA cannot be removed by UV radiation, H₂O₂ oxidation or micro‐aeration alone, while UV/H₂O₂/micro‐aeration combination processes have proved effective and can degrade this compound completely. With initial concentrations of about 110 μg/L, more than 95.1% of DCAA can be removed in 180 min under UV intensity of 1048.7 μW/cm², H₂O₂ dosage of 30 mg/L and micro‐aeration flow rate of 2 L/min. However, more than 30 μg/L of DCAA was left after 180 min by UV/H₂O₂ combination process without micro‐aeration with the same UV intensity and H₂O₂ dosage. The effects of applied UV radiation intensity, H₂O₂ dose, initial DCAA concentration and pH on the degradation of DCAA have been examined in this study. Degradation mechanisms of DCAA with hydroxyl radical oxidation have been discussed. The removal rate of DCAA was sensitive to operational parameters. There was a linear relationship between rate constant k and UV intensity and initial H₂O₂ concentration, which indicated that a higher removal capacity can be achieved by improvement of both factors. A newly found nitrogenous disinfection by‐product (N‐DBP)‐DCAcAm, which has the potential to form DCAA, was easier to remove than DCAA by UV/H₂O₂ and UV/H₂O₂/micro‐aeration processes. Finally, a preliminary cost comparison revealed that the UV/H₂O₂/micro‐aeration process was more cost‐effective than the UV/H₂O₂ process in the removal of DCAA from drinking water.     

Formation of hydroxyl radicals catalyzed by clay surfaces

 The formation of superoxide and hydroxyl radicals at the surface of smectite clays due to oxygen reduction is demonstrated by electron paramagnetic resonance spectroscopy. The yield of hydroxyl radicals is mainly a function of particle size of the clays and depends, to a lesser extent, on the clay lattice iron. Synthetic laponite clay with small platelet size (∼20 nm) and without lattice iron is leading in the formation of hydroxyl radicals followed by montmorillonite (∼200 nm). Fluorohectorite (∼2000 nm) was inactive to hydroxyl radical formation by oxygen reduction. Received: 20 January 2001 / Accepted: 7 August 2001     

荣成大疃刘家铍矿矿物赋存状态

大疃刘家铍矿铍元素主要以羟硅铍石单矿物赋存在矿石中。以羟硅铍石单矿物存在的BeO占79．45％;少部分分散在其他矿物中,以赤铁矿、褐铁矿中 BeO 含量较高,其次是绢云母、重晶石等。BeO 呈分散状态占20．55％,主要集中在绢云母中,这是由于矿石中绢云母含量高所致,分散状态的BeO无法回收。根据矿石中有用矿物和脉石矿物组合,矿石类型为羟硅铍石绢云母碳酸盐岩长石石英型铍矿石。     

Formation of black carbon-like and alicyclic aliphatic compounds by hydroxyl radical initiated degradation of lignin

Exposure of lignin-derived organic matter (OM) to hydroxyl radicals originating from Fenton type reactions generates condensed aromatic and alicyclic aliphatic compounds, as shown using ultrahigh resolution mass spectrometry. Although condensed aromatic compounds are common in soil and dissolved OM, their presence has been attributed largely to combustion. A non-pyrogenic route for the formation of condensed aromatic compounds from lignin is suggested here, specifically that hydroxyl radical-initiated oxidation of lignin is capable of producing black carbon-like condensed aromatic compounds. Alicyclic aliphatic compounds are also produced, likely as part of a concerted process involving ring opening, polymerization and/or cyclization and hydrogen abstraction. Hydroxyl radicals associated with lignin degradation are produced through photochemistry in aqueous systems and enzymatic microbial processes in soil.     

Effects of Operational Parameters on Decolorization of C. I. Acid Red 88 by UV/H2O2 Process: Evaluation of Electrical Energy Consumption

In the present study, effects of operational parameters on the electrical energy consumption for photooxidative process (UV/H₂O₂) for the decolorization of C. I. Acid Red 88 (AR88) have been investigated. In a series of experiments, 20 mg L^?1 of AR88 solution were irradiated in the presence of different concentrations of H₂O₂ (to find out optimum amount of H₂O₂) by UV light intensity of 30 W m^?2 for certain irradiation times. The decolorization of the dye followed pseudo first‐order kinetics, and hence, the figure‐of‐merit electrical energy per order (E_EO) is appropriate for estimating the electrical energy efficiency. The electrical energy consumption was determined during the variation of some parameters such as initial H₂O₂ concentration, initial dye concentration, UV light intensity, pH, and the gap size of solution. Results showed that electrical energy could be reduced by optimizing operational parameters.     

对流层大气氧化性研究进展

对流层大气氧化性是对流层大气自我清洁能力的一个重要指标,对流层中大多数痕量气体都是通过氧化过程清除的.回顾近半个世纪以来对流层大气氧化性的研究历史,对流层大气氧化性的研究无论是从测量技术还是模式研究方面都已取得了一定的进展.工业革命以来,由于人类活动的影响,CO、NOx和碳氢化合物等大气污染物排放增多,使得全球对流层大气OH浓度呈下降趋势,未来对流层大气氧化性的变化很大程度上也取决于这些气体的排放情况.利用全球三维大气化学传输模式MOZART研究中国地区对流层大气OH自由基的分布和变化趋势表明,与全球OH自由基变化趋势不同,近10年来中国东部地区OH自由基浓度趋于增加.未来对流层大气氧化性研究的关键问题仍是OH自由基测量技术的提高问题,OH自由基观测结果是完善对流层光化学机制和改进大气化学模式的先决条件.     

Treatment of Refractory Organics Contained in Actual Agro‐Industrial Wastewaters by UV/H2O2

In this work, the treatment of actual agro‐industrial wastewaters (IWW) by a UV/H₂O₂ process has been investigated. The aqueous wastes were received from industrial olive oil mills and then treated by laboratory scale physicochemical methods, i. e., coagulation using ferrous and aluminum sulfate, decantation, filtration and adsorption on activated carbon. These wastes are brown colored effluents and have a residual chemical oxygen demand (COD) in the range of 1800 to 3500 mgO₂ L^–1, which cannot be further eliminated with physicochemical processes. The UV/H₂O₂ treatments were carried out under monochromatic irradiation at 254 nm using a thermostated reactor equipped with a mercury vapor lamp located in an axial position. The effects of initial H₂O₂ concentration, initial COD, pH and temperature have been studied in order to determine the optimum conditions for maximum color and COD removals. The experimental results reveal the suitability of the UV/H₂O₂ process for both removal of high levels of COD and effectively decolorizing the solution. In particular, 95% of color removal and 90% of COD removal were obtained under conditions of pH = 5 and 32°C using 2.75 g H₂O₂ g^–1 COD L^–1 during 6 h of UV‐irradiation. The treatment is unaffected by pH over the range 2 to 9. In addition, the COD removal is improved by increasing the temperature, whereas the color removal has not been affected by this parameter. The results show that the hydroxyl radicals generated from the catalytic decomposition of H₂O₂ by UV‐irradiation of the solution could be successfully used to mineralize the organics contained in IWW. The mineralization of the organics seems to occur in three main sequential steps: the first is the rapid decomposition of tannins leading to aromatic compounds, which are confirmed by the decolorization of the IWW; the second step corresponds to the oxidation of aromatics leading to aliphatic intermediates, which occurs by the cleavage of an aromatic ring, and is established by the removal of aromatics, and the final step is the slow oxidation of the aliphatic intermediates, which is measured by the COD removal.     

新显色剂5-(3-羟基苯偶氮)-8-羟基喹啉与镍显色反应的研究与应用

本文研究了新显色剂５－（３－羟基苯偶氮）－８－羟基喹啉（５－ＨＡＨＱ）在十六烷基三甲基溴化铵（ＣＴＭＡＢ）存在下,ｐＨ４．４～５．６范围内与镍（ＩＩ）的显色反应,并拟定了光度法测镍的方法。镍与显色剂形成１∶４的稳定的红色配合物,ε４９５＝８．３６×１０４Ｌ·ｍｏｌ－４·ｃｍ－１,镍在０～０．７２μｇ／ｍｌ范围内遵循比耳定律。用于测定钢铁中微量镍,结果满意。