地球环境中的放射性污染

地球环境中的放射性污染有天然辐射来源和人为放射性来源,通过消化道、呼吸道和皮肤、粘膜或伤口进入人体内,对人体形成直接损伤、间接损伤和远期辐射效应,应从内照射和外照射防护两个方面来防止环境中的放射性污染.     

云南临沧矿产品开发中的放射性污染

临沧是我国铀矿资源地之一，本文在对当地多年的放射性矿及伴生放射性矿产产品开发中放射性污染问题进行了分析研究后，对目前采取的一些防治和管理措施进行了综合评价，对同类地区进行放射性污染管理具有借鉴作用。     

未熟-低熟烃源岩的有机岩石学特征

采用全岩光片镜鉴和显微荧光分析方法 ,对我国不同地区 5 0 0余块未熟 低熟烃源岩样品进行了系统的有机岩石学研究。未熟 低熟烃源岩显微组分组成具有显著的非均质性 ,不同地区显示出陆源组分与水生生源组分不同的“配比”关系 ,反映出其有机质组成的复杂性 ,并确认藻类体、孢子体、树脂体、木栓质体、壳屑体和矿物沥青基质等组分是其最常见的生烃组分。基于对镜质组反射率Ro和孢子体荧光变化等演化指标特征的分析 ,认为未熟 低熟烃源岩有机质早期热演化具有明显的阶段性 ,一般都表现为“二段式”变化 ,其变化界限大致以Ro等于 0 .5 0 %～ 0 .5 5 %为界。     

丁基锡化合物在水体悬浮颗粒物上的吸附行为研究

将海河河口表层底泥制成悬浮颗粒物（ＳＰＭ），采用批量平衡法首次研究了模拟河口条件下三丁基锡（ＴＢＴ）和二丁基锡（ＤＢＴ）在该ＳＰＭ上的吸附行为．结果表明，ＴＢＴ和ＤＢＴ均能在ＳＰＭ上发生吸附，尤以ＴＢＴ更为显著．吸附速率可用Ｋｕｏ和Ｌａｋｅ的经验公式描述；吸附过程受ＳＰＭ的浓度及ＴＯＣ含量、ｐＨ值、温度、腐殖酸浓度和盐度影响．实际河口水样中的ＳＰＭ对ＴＢＴ和ＤＢＴ的吸附百分率也较高，因此ＳＰＭ是ＴＢＴ和ＤＢＴ归趋的重要场所，去除ＳＰＭ可使水体得到一定净化．     

Characteristics of air particulate matter and their sources inurban and rural area of Beijing, China

ＩｎｔｒｏｄｕｃｔｉｏｎＴｈｅｒｅｉｓａｇｒｏｗｉｎｇａｗａｒｅｎｅｓｓｔｏｔｈｅｉｍｐｏｒｔａｎｃｅｏｆａｉｒｐｏｌｌｕｔｉｏｎｉｎｍａｊｏｒｃｉｔｅｓ.Ａｎｕｍｂｅｒｏｆｓｔｕｄｉｅｓｈａｖｅｓｈｏｗｎｔｈａｔｔｈｅｃｏｎｃｅｎｔｒａｔｉｏｎｓｏｆｃｅｒｔａｉｎｔｒａｃｅｅｌｅｍｅｎｔｓｉｎｔｈｅｕｒｂａｎａｔｍｏｓｐｈｅｒｅｈａｖｅｂｅｅｎｅｌｅｖａｔｅｄｂｙ ｐｏｌｌｕｔｉｏｎ ,ａｎｄｔｈｅｒｅｆｏｒｅ ,ｔｈｅｈｉｇｈｅｓｔｃｏｎｃｅｎｔｒａｔｉｏｎｓｏｆｔｈｅｓｅｃｈｅｍｉｃａｌｃｏｎｔ…     

淮南市采煤塌陷区水域的有机物污染研究

通过对淮南市采煤塌陷区水域理化指标和叶绿素的测定。用较为简单的W分级法对9个监测点的水质进行评分分级,并对塌陷区水域营养化程度进行了评级,用以反映采煤塌陷区的有机物污染状况。     

西湖底泥不同供氧条件下有机质降解及CO2与CH4释放速率的模拟研究

采用密闭培养实验装置于室温（２５℃左右）及ｐＨ为７５条件下，对西湖底泥中有机质完全降解及转化为ＣＯ２和ＣＨ４的速率进行了模拟研究．结果表明，在西湖湖水现有供氧水平（５０—８６ｍｇ（Ｏ２）／Ｌ）条件下，底泥中有机质完全降解的速率最为缓慢，培养期间（４２天）平均只有０７２ｍｇ（Ｃ）／（ｋｇ·ｄ）．当湖水供氧水平进一步上升（８６→１２０→１６０ｍｇ（Ｏ２）／Ｌ），ＣＯ２释放速率增加，最大值可达到８７ｍｇ（Ｃ）／（ｋｇ·周）；当湖水供氧水平下降（８６→０ｍｇ（Ｏ２）／Ｌ），ＣＨ４释放速率加快，最大值可达到４６ｍｇ（Ｃ）／（ｋｇ·周）．     

柯树背岩体铀金成矿远景分析

本文在研究柯树背岩体矿物岩石学特征基础上 ,通过对该岩体的铀金成矿元素丰度、铀金矿化类型、铀金矿石物质成分及成矿阶段的划分、矿脉的铀金含量及其相关关系、围岩蚀变及原生晕特点、铀金矿化控制因素的详细研究 ,从岩体的放射性地质地球化学特点、岩体蚀变及剥蚀强度、岩石化学及稀土元素地球化学、矿脉向深部的变化趋势等几个方面分析了该岩体的铀金成矿远景及今后找矿工作的意见 ,指出该岩体西体南部断续出现的柯树背—隘高断裂上盘 1km范围与下寮—大坑里断裂夹持区为铀金成矿远景区。     

序列间歇式好氧活性污泥法处理生物制药废水研究

本研究采用好氧ＳＢＲ法处理生物制药废水。试验结果表明，废水中不需另加氮磷营养物质，当进水ＣＯＤＣｒ为９１１～３２８０ｍｇ／Ｌ时，在曝气１６ｈ条件下，出水ＣＯＤＣｒ在３５０ｍｇ／Ｌ以下，ＢＯＤ５在８０ｍｇ／Ｌ以下，ＳＳ在１５０ｍｇ／Ｌ以下，皆达到生物制药工业废水二级排放标准。本文还对好氧ＳＢＲ法的有机物降解动力学过程进行了研究。     

Comparison of UV-based advanced oxidation processes for the removal of different fractions of NOM from drinking water

This study examined the effectiveness for degradation of hydrophobic (HPO), transphilic (TPI) and hydrophilic (HPI) fractions of natural organic matter (NOM) during UV/H₂O₂, UV/TiO₂ and UV/K₂S₂O₈ (UV/PS) advanced oxidation processes (AOPs). The changing characteristics of NOM were evaluated by dissolved organic carbon (DOC), the specific UV absorbance (SUVA), trihalomethanes formation potential (THMFP), organic halogen adsorbable on activated carbon formation potential (AOXFP) and parallel factor analysis of excitation–emission matrices (PARAFAC-EEMs). In the three UV-based AOPs, HPI fraction with low molecular weight and aromaticity was more likely to degradate than HPO and TPI, and the removal efficiency of SUVA for HPO was much higher than TPI and HPI fraction. In terms of the specific THMFP of HPO, TPI and HPI, a reduction was achieved in the UV/H₂O₂ process, and the higest removal rate even reached to 83%. UV/TiO₂ and UV/PS processes can only decrease the specific THMFP of HPI. The specific AOXFP of HPO, TPI and HPI fractions were all able to be degraded by the three UV-based AOPs, and HPO content is more susceptible to decompose than TPI and HPI content. UV/H₂O₂ was found to be the most effective treatment for the removal of THMFP and AOXFP under given conditions. C1 (microbial or marine derived humic-like substances), C2 (terrestrially derived humic-like substances) and C3 (tryptophan-like proteins) fluorescent components of HPO fraction were fairly labile across the UV-based AOPs treatment. C3 of each fraction of NOM was the most resistant to degrade upon the UV-based AOPs. Results from this study may provide the prediction about the consequence of UV-based AOPs for the degradation of different fractions of NOM with varied characteristics.