杂多酸水溶液脱除烟气中SO2的性能研究

合成了H3PMo12O40、H4SiW12O40、H3PW12O40、H4PMo11VO40、H5PMo10V2O40和H6PMo9V3O406种杂多酸,分别采用红外光谱(FT-IR)和X射线衍射(XRD)表征杂多酸的结构,并采用气相色谱仪对6种杂多酸水溶液进行脱硫实验测试.实验结果表明:制备的6种杂多酸具有良好的Ke...     

皂素提取头道液的典型有机物组成研究

利用紫外、红外拉曼光谱和GC/MS对传统皂素生产工艺、S-F工艺和E-S工艺头道液废水的有机物组成进行了分析。结果表明,传统工艺、S-F和E-S工艺头道液废水的有机物主要是醛类,此外,传统工艺头道液中检测到的22种有机物中,还有大量生物难降解的杂环类（12.24%）;而S-F和E-S工艺头道液中检测到的25种和31种有...     

微波消解-ICP—MS测定土壤和水系沉积物中的重金属

建立了一种采用逆王水和氢氟酸的混合体系微波酸消解土壤与水系沉积物,电感耦合等离子体质谱法快速测定六种金属元素（As、Cd、Pb、Cu、Cr和Ni）含量的方法。本文研究了消解温度和消解时间对消解效果的影响。结果表明,在190℃下运行25分钟对土壤与水系沉积物中的六种金属元素均具有很好的消解能力,备元素的测定值与标准值相符。在对实际土壤与水系沉积物样品进行分析后得出采样区域的土壤与沉积物中这六种金属含量水平正常。     

层状双氢氧化物去除水中磷的实验研究

研究了层状双氢氧化物处理高浓度含磷废水的可行性,考察了pH值、温度、吸附时间、振荡速度等因素对磷去除率的影响。结果表明,当pH值为7、反应温度为25℃、吸附时间为60min、LDH投加量为0.1g/50ml、磷初始浓度为500mg/L、震荡速度为150r/min时,磷的去除率高达94.82%,层状双氢氧化物对水中磷的吸附作用符合Langmiur等温方程。     

试论低碳经济背景下的政府职能

伴随着经济与社会的进步,能源短缺与环境污染正愈演愈烈,迫切需要由高碳经济转向低碳经济。中国目前的发展模式与消费结构仍处于高碳状态,因此发展低碳经济势在必行。政府作为经济活动的有机组成部分,应当在发展低碳经济的过程中履行好其对外交流、对内调控的政府职能。     

玛纳斯河流域生态系统服务功能价值研究

土地利用/覆被变化是生态环境演变最重要的因素之一,其研究对于促进区域生态经济协调发展有重要意义。根据1976年和2006年玛纳斯河流域两期遥感影像资料,基于生态经济学的最新方法采用卫星遥感技术以及Costanza等的生态系统服务价值评价手段,对期间玛纳斯河流域生态服务系统服务功能价值变化进行分析研究。结果表明:①玛纳斯流域土地利用结构变化在30年间表现为草地、林地、不断减少,而耕地、水域、沙地和建设用地不断增加,反映出人类因素及生态环境恶化的趋势;②该流域生态系统服务功能价值总额由1976年123.831 08元减少至2006年101.521 08元。减幅:18.02%,年均减少0.741 08元,通过对玛纳斯河流域生态系统服务功能价值进行评价,为玛纳斯河流域生态开发和治理,以及环境整治提供决策依据。     

Occurrence of monoethylmercury in the Florida Everglades: Identification and verification

A few studies have reported the occurrence of monoethylmercury (CH₃CH₂Hg⁺) in the natural environment, but further verification is needed due to the lack of direct evidence and/or uncertainty in analytical procedures. Various analytical techniques were employed to verify the occurrence of CH₃CH₂Hg⁺ in soil of the Florida Everglades. The identity of CH₃CH₂Hg⁺ in Everglades soil was clarified, for the first time, by GC/MS. The employment of the recently developed aqueous phenylation-purge-and-trap-GC coupled with ICPMS confirmed that the detected CH₃CH₂Hg⁺ was not a misidentification of CH₃SHg⁺. Stable isotope-tracer experiments further indicated that the detected CH₃CH₂Hg⁺ indeed originated from Everglades soil and was not an analytical artifact. All these evidence clearly confirmed the occurrence of CH₃CH₂Hg⁺ in Everglades soil, presumably as a consequence of ethylation occurring in this wetland. The prevalence of CH₃CH₂Hg⁺ in Everglades soil suggests that ethylation could play an important role in the biogeochemical cycling of Hg.     

基于重力加载比例法的岩质边坡稳定性分析

根据岩质边坡的稳定性主要由边坡内部的结构面所控制的特点,采用有限元重力加载比例法对含有一组平行节理面和含两组节理面的岩质边坡进行数值模拟,分析表明:与强度折减法相比,采用有限元重力加载比例法能更加快速地计算出岩质边坡的安全系数,节省计算耗时和人工干预的工作量,并能通过塑性应变的发展分析其破坏过程,确定潜在的滑动面。     

发展可再生燃料推进减排的现状和趋势

文章阐述了发展生物燃料可实现缓解石油供需矛盾和减排温室气体的双赢目的,介绍了世界各主要消费大国发展,应用生物燃料的情况及生物燃料的发展趋势.     

Influence of complex reagents on removal of chromium(VI) by zero-valent iron

The removal of Cr(VI) by zero-valent iron (Fe(0)) and the effect of three complex reagents, ethylenediaminetetraacetic acid (EDTA), NaF and 1,10-phenanthroline, on this reaction were investigated using batch reactors at pH values of 4, 5 and 6. The results indicate that the removal of Cr(VI) by Fe(0) is slow at pH 5.0 and that three complex reagents play different roles in the reaction. EDTA and NaF significantly enhance the reaction rate. The zero-order rate constants at pH 5.0 were 5.44 microM min(-1) in the presence of 4mM EDTA and 0.99 micrM min(-1) in the presence of 8 mM NaF, respectively, whereas that of control was only 0.33 micrM min(-1), even at pH=4.0. This enhancement is attributed to the formation of complex compounds between EDTA/NaF and reaction products, such as Cr(III) and Fe(III), which eliminate the precipitates of Cr(III), Fe(III) hydroxides and Cr(x)Fe(1-)(x)(OH)(3) and thus reduce surface passivation of Fe(0). In contrast, 1,10-phenanthroline, a complex reagent for Fe(II), dramatically decreases Cr(VI) reduction by Fe(0). At pH=4.0, the zero-order rate constant in the presence of 1mM of 1,10-phenanthroline was 0.02 micrM min(-1), decreasing by 99.7% and 93.9%, respectively, compared with the results in the presence and absence of EDTA. The results suggest that a pathway of the reduction of Cr(VI) to Cr(III) by Fe(0) may involve dissolution of Fe(0) to produce Fe(II), followed by reduction of Cr(VI) by Fe(II), rather than the direct reaction between Cr(VI) and Fe(0), in which Fe(0) transfers electrons to Cr(VI).