Adsorption of phenanthrene on Al (oxy)hydroxides formed under the influence of tannic acid

Although there has been substantial research done on adsorption of metals/metalloids by Al (oxy)hydroxides, little is known regarding the adsorption of polyaromatic hydrocarbons (PAHs) on Al (oxy)hydroxides, especially those formed in the presence of organic acid. This paper investigated the adsorption of phenanthrene on Al (oxy)hydroxides formed with initial tannate/Al molar ratios (MRs) 0, 0.001, 0.01, and 0.1 (referred to MR0, MR0.001, MR0.01, and MR0.1, respectively) through batch adsorption experiments and FTIR study. The results showed that Al (oxy)hydroxides were important sorbents for phenanthrene. The adsorption kinetic data were fitted well with the pseudo-second-order equation. According to a modified Freundlich model, the adsorption capacities of Al (oxy)hydroxides followed a descending order of MR0.1 > MR0 ≥ MR0.01 > MR0.001, which was inconsistent with the organic carbon content in the Al (oxy)hydroxides. Adsorption capacity correlated with the specific surface area, micropore area, and micropore diameter of Al (oxy)hydroxides, yet the relationships were not statistically significant (P > 0.05). FTIR results showed that physical interaction was essential in phenanthrene adsorption onto the Al (oxy)hydroxides, which could be explained by an entropy-driven process. Surface hydrophobicity of Al (oxy)hydroxides played a key role in phenanthrene adsorption. Additional π–π electron donor–acceptor interaction of phenanthrene (acting as electron donor) with aromatic ring of tannic acid (electron acceptor) could be also important in phenanthrene adsorption by high MR Al (oxy)hydroxides, yet it needs further study. The findings obtained in the present study are of fundamental significance in understanding the mechanism of immobilization of PAHs in low organic matter but oxide-rich soils.     

岩浆-流体过渡和阿尔泰三号伟晶岩脉之成因

本文对新疆阿尔泰可可托海的三号伟晶岩形成的物理化学条件、特别是流体-熔融包裹体进行了研究，证明岩浆的确可以分出热液，对于三号伟晶岩脉来说，这种热液组分主要是NaCl－CO2－H2O流体。     

南秦岭东江口、柞水岩体岩石谱系单位划分及演化

南秦岭东江口、柞水岩体位于南丹断裂带南侧,为华力西期岩基。通过1：5万地质填图,将东江口老体划分为5个岩石谱系单位,柞水岩体划分为3个岩石话系单位,共圈定出36个侵入体。分别建立了东江口超单元和排水超单元。依据接触关系,结构构造,包体特征确定了其侵入序次,构成了两个完整的“S”型岩浆演化序列,在岩石矿物组成、岩石化学成分、微量元素及稀土元素组成上,各具有明显的独特岩浆演化特征,分别形成于南秦岭晚古生代被动陆线构造环境。     

Pretreatment of high strength waste emulsions by combined vibratory shear enhanced process with Fenton oxidation

Pretreatment of waste emulsions with high organic content by a combined process of vibratory shear enhanced process and Fenton’s oxidation prior to biological treatment was investigated. Vibrating membrane had shown good performance in chemical oxygen demand and oil removals and the mitigation of concentration polarization. However, the permeate after filtration processing still contained high content of organics. Thus, additional Fenton oxidation was applied to reduce the organic loading, and improve the biodegradability of the wastewater. The optimal molar ratio of ferrous iron to hydrogen peroxide was 0.05 obtained from the jar-test experiments. Removal of organics was enhanced by increasing hydrogen peroxide dosage, while efficiency of hydrogen peroxide reached maximum of 1.11(w/w) at the hydrogen peroxide dosage of 6.8 g/L. Furthermore, the biological experiments indicated that the high concentration of organics could inhibit microbial activity, which decreased the chemical oxygen demand degradation rates. The adaptive period of the microbe was greatly shortened using Fenton’s reagent at the low dosages. The improvement of the biodegradability could be explained by partial mineralization and chemical transformation of parent organic compounds after Fenton oxidation.     

小体积萃取-石墨炉原子吸收法测定高纯硝酸钡中纳克级重金属元素

本文研究了石墨炉原子吸收光谱法测定高纯硝酸钡中超痕量重金属元素的分析技术。提出在大量钡基体存在时,采用小体积萃取体系APDC-MIBK同时萃取纳克级的Fe、Cu、Co和Ni。该法具有灵敏度高、无干扰、操作方便和减少沾污等特点。方法检出限为:Fe 7.2ng/g、Cu 12.8ng/g、Co 4.4ng/g和Ni 6.7ng/g。应用于红外光纤原料硝酸钡、硝酸铝中痕量重金属的测定,效果良好。     

长春黄土状土的水文、工程地质特性及降水方案的确定

在镜下对长春黄土状土的微观结构进行研究，发现第三层粉质粘土含水机制在于土中具有纵横交织的空洞和管道，地下水赋存于其中；第二层棕红色粉质粘土和粘土的崩解性在于该层土具有网状裂隙，卸荷后遇水崩解，在此基础上提出基坑降水的设计方案。     

Li_2O-(Mg、Zn、Ni)O-V_2O_5三元体系的相平衡

对Li_2O-(Mg、Zn、Ni)O-V_2O_5三元体系在500—800℃相图的研究表明,在每个系统内部都出现了一个依端员组分摩尔比为1:2:1的化合物。即橄榄石型的LiMgVO_4,硅铍石型的LiZnVO_4和尖晶石型的LiNiVO_4。不同的是,Li_2O-MgO-V_2O_5中发现了第二个三元相和一个固溶体。LiO_2-NiO-V_2O_6中得出一个固溶体,而LiZnNO_4中未得固溶体。     

塔里木盆地原油的轻烃分类及成因研究

通过对塔里木盆地不同地区不同层位205个原油样品的色谱分析研究,应用其轻烃的组分作关系图,将塔里木盆地原油划分为海相油(A)、湖相油(B)和煤成油(C)三大类。海相烃源岩中过渡金属及其配位体结构有利于五环优势,导致其生成的海相原油(A)具五环优势;陆相烃源岩中过渡金属及其配位体结构有利于三环优势和六环优势,导致其生成的陆相原油(B,C)具三环优势和六环优势。应用正庚烷值与异庚烷值作关系图,将塔里木盆地原油划分为海相油(A)、陆相油(B+C)两大类。海相油(A)沿脂肪族干酪根曲线分布,陆相油(B+C)大多沿芳香族干酪根曲线分布。对于同类烃源岩,随着埋深和压力不断增加,烃源岩中干酪根自由体积将不断减小,对六环优势抑制最大,对五环优势抑制较大,对三环优势抑制较小,对直接裂解抑制最小,导致其生成的原油中正庚值和异庚烷值随埋深增加而增加。     

煤的变质程度对焦炭结构构造的影响

从宏观和微观两方面对不同变质程度煤所形成焦炭的结构、构造进行了深入研究。从气煤到肥煤阶段（Ｒｏ，ｍ：０．７７％～１．１６％），焦炭气孔壁厚度逐渐增大；进入焦煤阶段（Ｒｏ，ｍ＞１．１６％），焦炭气孔壁厚度降低。气煤、１３焦煤形成的焦炭结构以各向同性体为主，焦煤、肥煤炼出的焦炭以粒状镶嵌结构为主。由气煤和高变质程度的焦煤形成的焦炭，其气孔以微孔和大孔为主，气孔分布标准差Ｄｓ最大；肥煤炼出的焦炭，其气孔分布大小较均一；１３焦煤和低变质程度的焦煤成焦后，气孔分布状况介于上述二者之间     

硅酸盐固溶体矿物中组分的韵律型空间分布及形成过程中的时-空自组织

本文根据熔体聚合模型和正规溶液模型,建立了非平衡条件下,在二组分硅酸盐熔体固结过程中的非平衡非理想界面反应的非线性动力学模型:对上式进行数值模拟表明,当W/RT<-2时,有三重态,并通过建立界面状态(组成)的质量守恒方程,合理地说明了硅酸盐固溶体矿物韵律结构形成的可能机理之一,寻找界面反应三重态是研究固溶体矿物韵律结构的一条相当普遍的途径。