褐煤经磺化及碱化处理对重金属离子吸附性能研究

褐煤经磺化和碱化处理对褐煤吸附重金属的性能影响显著,通过对金属离子Ｃｕ＾２＋,Ｐｂ＾２＋,Ｚｎ＾２＋,Ｃｄ＾２＋,Ｎｉ＾２＋的单组分或多组分溶液进行吸附研究,对比了吸附速率、吸附容量、吸附选择性、耐酸性以及抗干扰能力等方面的差异,探讨了磺化褐煤和碱化褐煤对重金属离子的吸附机理,指出了今后的研究方向。     

水杨醛改性壳聚糖对金属离子的吸附性能

研究了以水杨醛改性的壳聚糖及其衍生物对Ｐｂ＾２＋、Ｚｎ＾２＋，Ｃｏ＾２＋的静态吸附性能，结果表明，该类吸附剂对Ｐｂ＾２＋，Ｚｎ＾２＋具有良了的吸附性能，其吸附量可分别达４５５．２和１０５．５ｍｇ·ｇ＾－１，并能在Ｃｏ＾２＋存在下选择吸附Ｐｂ＾２＋，Ｚｎ＾２＋。     

铬、镉、铅胁迫对青菜叶片几种生理生化指标的影响

研究了溶液培养条件下铬、镉、铅胁迫对青菜叶片细胞膜透性、叶绿素含量和游离脯氨酸含量等的影响,结果表明：随着Ｃｒ＾６＋,Ｃｄ＾２＋,Ｐｂ＾２＋处理时间的延长和处理浓度的增加,青菜叶片细胞膜透性显著增大,叶绿素ａ／ｂ值逐渐降低,游离脯氨酸含量明显增加,其中游离脯氨酸含量增加的时间比细胞膜透性增大明显超前,而叶绿素ａ／ｂ植降低的时间在这３种重金属中未见明显的规律性。     

产中性纤维素酶芽孢杆菌Y106产酶条件优化

筛选得到一株高产中性纤维素酶的芽孢杆菌Ｙ１０６,并对其发酵条件进行了优化,麸皮能够较大幅度地促进产酶,果糖是良好的诱导物,有机氮流促进产酶的效果优于无机氮源,最优的有机氮源是蛋白胨。Ｆｅ＾３＋、Ｆｅ＾２＋、Ｎａ＾＋、Ｃａ＾２＋可以促进纤维素酶的合成,而Ｃｕ＾２＋、Ａｇ＾＋、Ｃｏ＾２＋、Ｈｇ＾２＋则对合成起遏制作用,在酶反应系统中Ｆｅ＾３＋、Ｆｅ＾２＋、Ｃａ＾２＋、Ｍｇ＾２＋能激活纤维素酶活性,Ｃｏ     

华北地区城市地下水中主要离子含量升高机理分析——以洛阳市为例

本文以洛阳市为例，讨论了华北地区地下水中主要离子的背景浓度及其形成作用。在此基础上，重点阐述了地下水中Ｃａ＾２＋，Ｍｇ＾２＋浓度升高的若干机理，并对污染源各不相同的三个水源地地下水Ｃａ＾２＋，Ｍｇ＾２＋浓度升高机理进行了定量分析，比较了Ｃａ＾２＋，Ｍｇ＾２＋浓度与其它主要离子浓度的相关特征，研究表明：该区两类地下水主要形成了钙长石和镁榄石的风化作用，地下水中ＣＯ２分压升高，可促进Ｃａ，Ｍｇ硅酸盐，     

黄棕壤和红壤吸附磷酸根后对Zn^2＋和Cd^2＋次级吸附的动力学

本文用流动法考察湖北省黄棕壤和湖南省红壤吸附磷酸根后，对Ｚｎ＾２＋和Ｃｄ＾２＋次级吸附的动力学。结果表明，Ｚｎ＾２＋和Ｃｄ＾２＋的次级吸附动力学可用一级议程拟合。初级吸附的磷酸根可造成黄棕壤对Ｚｎ＾２＋和Ｃｄ＾２＋次级吸附的速率下降；而红壤对Ｚｎ＾２＋和Ｃｄ＾２＋次级吸附的快反应速率下降，慢反应速率加大。Ｚｎ＾２＋和Ｃｄ＾２＋浓度增高可加快次级吸附反应速率；升高温度也可增快次级吸附速率。扩散作用对     

交联壳聚糖乙酯酯冠醚对金属离子的吸附性能研究

本文合成了二苯并－１６－冠－５－氯代乙酸酯冠醚和３，５－二叔丁基－二苯并－１４－冠－４－双氯代乙酸酯冠醚 ，然后分别将之与交联壳聚糖反应，制备了交联壳聚糖二苯并－１６－冠－５－乙酸酯冠醚 和交联壳聚糖３，５－二叔丁基－二苯并－１４－冠－４－双乙酸酯冠醚，并研究了它们对Ｐｂ＾２＋，Ｃｕ＾２＋，Ｃｒ＾３＋，Ｎｉ＾２＋，Ｃｄ＾２＋的吸附性能。结果表明这两种吸附剂对Ｐｂ＾２３＋，Ｃｕ＾２＋有较高的吸附选择     

可变电荷土壤和矿物表面Cu^2＋吸附过程中H^＋释放动力学

本文以硝酸根离子选择电极为参比电极,低阻ｐＨ玻璃电极为指示电极,研究了红壤和高岭石体系Ｃｕ＾２＋吸附过程中ｐＨ的变化情况,并通过红壤和高岭石的酸碱滴定曲线求得了不同反应时间Ｈ＾＋释放的绝对量,即Ｈ＾＋释放动力学。结果表明,Ｃｕ＾２＋吸附过程中Ｈ＋释放大部分在反应刚开始时进行,反应进行５ｍｉｎ后,两种Ｃｕ＾２＋起始反应浓度的高岭石和红壤体系Ｈ＋分别释放了９２％和８２％以上。Ｃｕ＾２＋起始反应浓度愈大     

国外关于稳定化/固化的有毒有害污染物的渗漏实验方法的研究进展

以水泥为基质的稳定化 /固化 (Stabilization/solidification)的方法在国外广泛用于无机、有机、有毒有害污染物的最终处置 ,已经有数十年的历史。论文较全面地介绍了拟合被这种稳定化 /固化过程处理过的污染物在自然界条件下短期和长期的污染物泄漏过程 ,即所谓短期、长期的渗漏行为的实验方法和数学模型 ,并总结了现有几种用来模拟短期或长期渗漏行为的渗漏实验方法和适用于这些实验方法的数学预测模型的应用条件。     

青霉菌BS—1还原Cr^6＋的条件及影响因子

青霉菌ＢＳ－１生长时还原Ｃｒ＾６＋的条件下：最适碳源为蔗糖或糊精，最适氮源是硫酸铵，最适温度３０℃，最适ＰＨ７．０，加入一定浓度的酵母浸出物可促进该菌对Ｃｒ＾＋的还原。不同预培养条件对该菌还原Ｃｒ＾６＋无明显影响，由此认为该菌对Ｃｒ＾６＋的还原是非诱导性的Ｈｇ＾２＋，Ｃｕ＾２＋，Ｃｏ＾２＋和Ｎｉ＾２＋对ＢＳ－１生长及Ｃｒ＾２｜还在有明显抑制作用，但在ρ（Ｎａ２ＳｅＯ４）＝１００ｍｇ／Ｌ时，则对该菌     

镍钴采选行业废石和尾矿中重金属淋溶释放规律研究

镍钴采选废石和尾矿中重金属的溶出释放规律对矿区的重金属污染防治具有重要意义。但目前,国内还没有对镍钴行业采选产生的尾矿和废石中重金属的溶出规律开展研究。本文以镍钴采选企业的尾矿和废石作为样本,开展了毒性浸出实验。研究了不同pH值、离子强度、温度等实验条件对重金属溶出的影响,探讨了镍钴采选过程中所产生的尾矿和废石中重金属的溶出特性和释放规律。实验结果表明,尾矿样品中Ni的浸出浓度为42.28 mg·L^-1,是最大允许排放浓度的8.86倍,为具有浸出毒性特征的危险废物;废石样品中重金属Ni和Cu的溶出浓度分别为4.72 mg·L^-1和26.2 mg·L^-1,超过最大允许排放浓度,属于第Ⅱ类一般工业固体废物。pH对样品中Ni、Cr、Pb、Co和As的溶出量影响较大,其中尾矿中Ni和Cu在pH较低的条件下,可达到44.28 mg·L^-1和53 mg·L^-1,远高于最大允许排放浓度,而Hg、Cd和Cu的溶出量随pH值的变化不大。除As以外,样品中大多数重金属的溶出质量浓度在酸性条件下比在中性条件下高,这表明在酸性环境条件下,这些重金属对周围生态环境的潜在风险更大。离子强度的变化对Cd和Co的溶出量的变化并不明显,而当离子强度变化时,Ni、Cr、Pb、Hg、Cu和As的溶出量可能达到最大,使周围环境的潜在生态风险增大。当温度达到35~40℃时,部分重金属如Co、Pb、Cd 等,溶出量将达到最大;当温度低于25℃时,除 Ni 以外,大部分重金属溶出量很低。而温度变化对重金属Cu、As、Cr和Hg的溶出量的影响不明显,波动范围较小,对周围生态环境产生的潜在生态风险较小。     

Chemical Behaviour of Calcium in Stabilized Oil Ash Reef Blocks After Five Years in the Ocean

Reef blocks made from stabilized oil ash were taken from the sea after five years in the ocean to examine the chemical behaviour of calcium. Experiments included (1) determination of the calcium leaching rate and a comparison with the rate for unexposed blocks to test the validity of a diffusion model for predicting long term (5 years) leaching rates, (2) determination of the effect of biological cover (shell) on the leaching rate, (3) determination of the leaching rate of the core of exposed reef blocks, (4) determination of the calcium content in 'ring areas' - regions of discoloration observed in sectioned exposed reef blocks, and (5) determination of the leachable fraction of the total calcium in exposed reef blocks. Results showed the presence of a pronounced calcium discontinuity zone located 3-7 cm from the outside surface of the reef blocks. Cumulated calcium release rates ranged from 2.81-3.14 μmol cm^-2 day^-1 for original unexposed reef blocks and the core of exposed (in the ocean for five years) blocks, respectively, to 0.47-0.50 μmol cm^-2 day^-1 for outside (facing sea water) surfaces of exposed reef blocks. Tank leaching studies also showed that the presence or absence of hard biological cover (shells) had little or no effect on the calcium release rate. the diffusion model normally used in modelling the chemical behaviour of calcium cannot be used to predict the long term (five years) leaching of calcium. the core of the exposed blocks released calcium at a rate similar to new, unexposed reef block material. Overall, it appears that the calcium discontinuity zone is probably responsible for restricting the release of calcium and hence the failure of the diffusion model.     

Chemical Behaviour of Calcium in Stabilized Oil Ash Reef Blocks After Five Years in the Ocean

Abstract

Reef blocks made from stabilized oil ash were taken from the sea after five years in the ocean to examine the chemical behaviour of calcium. Experiments included (1) determination of the calcium leaching rate and a comparison with the rate for unexposed blocks to test the validity of a diffusion model for predicting long term (5 years) leaching rates, (2) determination of the effect of biological cover (shell) on the leaching rate, (3) determination of the leaching rate of the core of exposed reef blocks, (4) determination of the calcium content in ‘ring areas’ - regions of discoloration observed in sectioned exposed reef blocks, and (5) determination of the leachable fraction of the total calcium in exposed reef blocks. Results showed the presence of a pronounced calcium discontinuity zone located 3–7 cm from the outside surface of the reef blocks. Cumulated calcium release rates ranged from 2.81–3.14 μmol cm^?2 day^?1 for original unexposed reef blocks and the core of exposed (in the ocean for five years) blocks, respectively, to 0.47–0.50 μmol cm^?2 day^?1 for outside (facing sea water) surfaces of exposed reef blocks. Tank leaching studies also showed that the presence or absence of hard biological cover (shells) had little or no effect on the calcium release rate. the diffusion model normally used in modelling the chemical behaviour of calcium cannot be used to predict the long term (five years) leaching of calcium. the core of the exposed blocks released calcium at a rate similar to new, unexposed reef block material. Overall, it appears that the calcium discontinuity zone is probably responsible for restricting the release of calcium and hence the failure of the diffusion model.     

生态水泥中重金属测定方法研究

生态水泥中的重金属问题已经成为制约水泥回转窑混烧废物技术发展的重要因素。文章从总量及浸出性质两个方面分析了现有的重金属测定方法,并通过试验分析了各方法的特点与适用性。试验结果表明:(1)荧光光谱法是最优的总量测定方法;(2)目前我国常用的浸出毒性测定方法不适用于水泥体系;(3)长期浸泡方法可用于测定特定条件下重金属的长期浸出性。这些结论为制定水泥窑混烧危险废物技术的标准与规范提供理论依据。     

保护地番茄养分利用及土壤氮素淋失

在施用不同复合肥料的条件下,对保护地蔬菜蕃茄对N、P、K养分的吸收利用及保护地条件下土壤的硝酸盐淋洗进行了研究,结果表明,复合肥的品种及施肥水平对番茄的产量影响不大,与CK相比番茄果实增产12．．7％－18．4％;复合肥N、P养分的当季利用率不足10％,而K素的当季利用率也不超出25％,传统的大水漫灌条件,蔬菜保护地土壤硝酸盐的淋洗状态相当严重,并有可能造成地下水的硝酸盐污染,长期过量施肥及大小漫灌等措施是造成土壤养分累积、硝酸盐淋洗严重、肥料利用率低的根本原因,图2表3参11     

热带亚热带多雨湿润区旱地土壤氮肥淋溶损失模拟研究

用土柱研究旱地土壤60cm土体夏季的氮肥淋溶损失,结果表明,在土壤施尿素后35d内淋水350mm,在不产生泾流的条件下,淋失率平均为25．5％。还探讨了氮肥淋溶过程中的氮形态变化,以及施氮量和土层深度对氮肥淋浴损失的影响。     

Characteristics of the stabilized/solidified municipal solid wastes incineration fly ash and the leaching behavior of Cr and Pb

Fly ash is a hazardous byproduct of municipal solid wastes incineration (MSWI). An alkali activated blast furnace slag-based cementitious material was used to stabilize/solidify the fly ash at experimental level. The characteristics of the stabilized/solidified fly ash, including metal leachability, mineralogical characteristics and the distributions of metals in matrices, were tested by toxic characteristic leaching procedure (TCLP), X-ray diffraction (XRD) and scanning electron microscopy-energy dispersive spectrometer (SEM-EDS) respectively. Continuous acid extraction was utilized to extract metal ions and characterize their leaching behavior. The stabilization/solidification procedure for MSWI fly ash demonstrates a strong fixing capacity for the metals by the formation of C-S-H phase, hydrated calcium aluminosilicate and ettringite. The stabilized/solidified fly ash shows a dense and homogeneous microstructure. Cr is mainly solidified in hydrated calcium aluminosilicate, C-S-H and ettringite phase through physical encapsulation, precipitation, adsorption or substitution mechanisms, and Pb is mainly solidified in C-S-H phase and absorbed in the Si-O structure.     

微胶囊EDTA对2种土壤中铅释放的影响

选用不同铅污染程度及pH值的土壤,采用连续批浸提实验和土柱淋溶实验,比较研究微胶囊EDTA（Cap-EDTA）和未微胶囊化EDTA（Ncap-EDTA）对不同土壤溶液中pH值和铅离子浓度动态变化影响,以及土壤渗滤液中铅离子淋失特征。结果表明：施加2种不同形式的EDTA,可极显著地增加土壤溶液中铅离子浓度,Cap-EDTA能控制土壤溶液中铅浓度的突增幅度,且使土壤溶液中的铅持续保持在适度浓度的时间更长。同一种土壤不同处理间土壤pH值的变化趋势基本一致,无显著差异。施用2种不同形式EDTA可极显著地增加土壤渗滤液中铅离子含量,土壤铅累积淋失量呈对数曲线上升,但施用Cap-EDTA处理能显著降低土壤中铅的初始淋失量和淋失总量。在相同浓度及形式的EDTA下,高铅浓度和高pH值的土壤铅更易活化和淋失。因此,在进行污染土壤植物修复的EDTA调控时,采用微胶囊化EDTA,能降低其带来的污染地下水风险。     

包膜控释和常用氮肥氮素淋溶特征及其对土水质量的影响

大量施用氮素化肥所引起的氮素损失和环境污染正日益受到重视。通过土柱模拟氮素养分的淋洗试验,探讨包膜控释氮肥和常用氮肥的氮素淋失特点及其对土壤和地下水质量的影响。研究结果表明,不同氮肥施入土壤后氮素的淋失率有着显著的差异,其中硝酸钾中氮素淋失率最高,其次为尿素,硫酸铵和碳铵的氮素淋失量明显较小。然而控释氮肥因其控制释放的特点,在氮素释放的高峰期,其模拟淋失量较高,但如果在田间条件下此释放高峰期与作物吸肥高峰期相吻合,则会显著地降低其淋失率。除尿素外,被淋失的氮素均以硝态氮为主,尿素则以酰胺分子态被淋溶。大量速效化肥的施入会形成土壤中的肥料"微域点",引起交换性Ca2+、Mg2+离子的淋失,从长远来看可引起土壤结构的破坏,而施用控释肥则很少形成这种"微域点",有利于土壤结构和肥力的维持。不同氮肥处理淋洗后对土壤pH值和有效氮含量变化的影响差异较大,其中以控释肥对土壤pH值变化的影响较小。大多数氮肥处理在淋洗后,土壤中各层速效氮含量较淋洗前有所降低,然而两种控释氮肥处理的土壤表层却能持续保持较高的有效氮含量。