南京及邻近地区新近沉积土的动剪切模量和阻尼比的试验研究

通过对南京及其邻近地区漫滩相成因的粘土、粉质粘土、淤泥质粉质粘土、粉质粘土与粉砂互层土、粉土、粉细砂等 6类新近沉积土的自振柱试验 ,详细探讨了围压大小、剪应变水平、土的颗粒组成和结构性对这 6类新近沉积土的剪切模量G及阻尼比λ的影响。通过与Seed和Idriss建议的砂土G/Gmax～γ和λ～γ曲线变化范围的对比 ,结果表明 ,不能将粉质粘土与粉砂互层土简单地当作砂土或粉质粘土对待。通过试验和理论分析 ,给出了南京及其邻近地区 6类新近沉积土动剪切模量和阻尼比随剪应变变化的平均曲线的拟合曲线、包络线及其参数的推荐值 ,对实际工程具有一定的借鉴作用     

Decontamination of Cr(VI) facilitated formation of persistent free radicals on rice husk derived biochar

PFRs were produced on biochar during Cr(VI) decontamination. PFRs formation on biochar was owing to the oxidization of phenolic-OH by Cr(VI). Appearance of excessive oxidant led to the consumption of PFRs on biochar. Biochar charred at high temperature possessed great performance to Cr(VI) removal. This study investigated the facilitation of Cr(VI) decontamination to the formation of persistent free radicals (PFRs) on rice husk derived biochar. It was found that Cr(VI) remediation by biochar facilitated the production of PFRs, which increased with the concentration of treated Cr(VI). However, excessive Cr(VI) would induce their decay. Biochar with high pyrolysis temperature possessed great performance to Cr(VI) removal, which was mainly originated from its reduction by biochar from Inductively Coupled Plasma Optical Emission Spectroscopy and X-ray Photoelectron Spectroscopy. And the corresponding generation of PFRs on biochar was primarily ascribed to the oxidization of phenolic hydroxyl groups by Cr(VI) from Fourier Transform Infrared Spectroscopy analysis, which was further verified by the H₂O₂ treatment experiments. The findings of this study will help to illustrate the transformation of reactive functional groups on biochar and provide a new insight into the role of biochar in environmental remediation.     

On the parameterization of the roughness length for the air-sea interface in free convection

The roughness length at the air-sea interface during free convection (z_0fc) is mainly related to the convective velocity (w_*) rather than the friction velocity (u_*). The parameterization of z_0fc with w _* ² /g as proposed by Abdella and DAlessio in 2003 is evaluated. It is shown that their proposed formula is consistent with field measurements. In order to avoid self-correlation by using u_*, a new parameterization of w_* with wind speed (U_z) at height z and stability parameter (z/L, where L is the buoyancy length) is proposed. This new formula for w_* is in agreement with an independent field result.     

吸烟气相物质引起的脂质过氧化的研究

本文用吸烟气相物质作用于卵磷脂形成的脂质体及人多形核白细胞,用TBA法和共轭二烯法检测吸烟气相物质作用下的脂质过氧化水平,结果发现,随着吸烟气相物质作用时间的延长,MDA和共轭二烯的含量也随之增大。表明吸烟气相物质能够引起脂质过氧化反应。     

Hg2+胁迫下玉米生理生态变化的研究

通过砂培实验,研究汞胁迫下玉米的生理生态指标包括叶绿素含量、根系活力、游离脯氨酸含量的变化.结果表明,汞对玉米的胁迫是浓度和时间双重因子的作用在低汞浓度、短时间内,叶绿素含量、根系活力及游离脯氨酸含量均有上升的趋势;在高汞浓度、长时间内,各生理指标均严重下降.各生理指标对汞的敏感度略有差异游离脯氨酸含量>根系活力>叶绿素含量;其中脯氨酸含量可以作为汞污染的一个监测指标.     

Humic acid and free radical in environment of Kaschin-Beck disease areas

The humic acid contents in drinking water and soil in Kaschin-Beck disease areas were found more than that of non-disease areas in this research. Changes of free radical concentration in drinking water were agreed with that of humic acid contents in drinking water of Kaschin-Beck disease areas. A positive correlation of free radical concentration and humic acid content in drinking water has been shown (r=0.913) . The structure of I. R. spectra of humic acid under ultraviolet light has been changed. Thus it indicated that free radical was resulted from benzoqiunonyl groups of humic acid in environment.     

黄腐酸与镰刀菌代谢产物的ESR谱性质的研究

以ESR谱仪为主要工具,配合大骨节病病因研究,进行了有关地区饮水中有机物,主要是腐殖酸的黄腐酸级分和粮食真菌——镰刀菌代谢产物性质的相似性比较研究.结果发现,病区粮食中自由基浓度高于非病区,而尖孢镰刀菌(Fusarium Oxysporum)浸染使玉米粉的自由基浓度增加.在氧化、还原、加热和改变酸碱度等处理过程中,菌粮自由基的ESR谱表现出和黄腐酸同样的变化规律.菌粮水提液经GDX-102树脂吸附后,其ESR谱和pH值的关系表明,镰刀菌代谢产物中的自由基集中于带有酸性基团的分子上.水提液的紫外及荧光光谱和黄腐酸具有一定的相似性,因而推论镰刀苗代谢产物的自由基与黄腐酸一样,都是半醌自由基.最后就这类自由基和大骨节病的关系进行了讨论.     

·OH的形成机理及在水处理中的应用

以产生大量·OH为特点的高级氧化水处理技术已逐渐成为各国水处理技术研究的热点。在讨论·OH氧化能力的同时 ,重点讨论了Fenton法、纳米光催化氧化法、电化学催化降解法以及超声降解法·OH的形成机理 ,介绍了它们在水处理中的工业化应用及进展情况 ,展望了今后在该领域中多种氧化降解方法协同作用的发展方向     

A straightforward synthesis in aqueous medium of enantiomerically enriched S(-)2,2′-dihydroxy-1,1′-binaphthyl

Chiral, atropisomeric 2,2'-dihydroxy-1,1'-binaphthyl has been extensively used to direct asymmetric processes. Its key role in asymmetric catalysis has spurred efforts to synthesize it in the optically pure form, but the reported synthetic routes have a significant environmental impact. In an aqueous peroxydase-cyclodextrin system the oxidative coupling of 2-naphthol took place very rapidly in almost quantitative yield and resulted in an enantiomeric excess. This one-pot synthesis do not require any organic solvents and oxidising metal cations.