武汉市一组复合氧化塘藻类与某些生态因子的相关性研究

报道了从1988年3月至1989年12月对武汉市墨水湖地区一组复合氧化塘中藻类总细胞数(ACN)、叶绿素a(chl·a)与水温、透明度、总氮(TN)、总磷(TP)、总溶解磷(TDP)、溶解磷(DP)、非溶解磷即总磷与总溶解磷之差值(TP-TDP)等的相关性及ACN与chl·a的相关性的研究结果,并讨论了这些相互关系对氧化塘处理效果、氧化塘水质变化的指示意义.     

产冷适应复合酶菌株Pseudomonas sp.NJ197的选育、发酵条件及酶学性质

从南极普利兹湾深海沉积物中筛选到一株同时产多种冷适应酶的菌株NJ197,细菌学形态鉴定及16S rDNA序列分析表明,该菌株属于假单胞菌属(Pseudomonas).生长特性研究表明,该菌株属于耐冷菌,其最适生长温度为5~15℃.NJ197菌株能利用多种单一的碳、氮源产酶,最适产酶温度为20℃,最高产酶温度为30℃.粗酶液经硫酸铵盐析、DEAE cellulose-52柱层析初步分离纯化后进行酶学性质的研究.该菌株所分泌复合酶中脂肪酶和淀粉酶的活力最高,它们的最适作用温度分别为30℃和35℃,最适pH值分别为9.0和9.5,对热敏感,是典型的碱性冷适应复合酶.Ca2 、Mn2 、Cu2 、Co2 、Fe3 对该复合酶有较为明显的激活作用,而Zn2 、Hg2 、Rb2 、Cd2 、EDTA则能抑制酶活.其中脂肪酶能在高浓度的SDS、CHAPS等变性剂中表现出较好的稳定性.图5表2参21     

新旧常态中国产业全碳足迹复杂网络比较

国民经济是由多个性质迥异且相互依赖产业构成的复杂系统,科学识别产业碳排放关联传导结构对于实现中国碳减排目标具有的重要理论及现实意义。为此,首先从直接和间接两个角度综合定义全碳足迹,基于能源消耗及生产服务修正直接消耗系数,创立函数改进容许性,及时更新投入产出表,夯实数据来源基础。再设计平衡性投入产出产业全碳足迹生命周期模型测算产业全碳足迹,基于WT指数法构建新旧常态中国产业全碳足迹复杂网络,继而从网络整体、节点地位、社团结构等角度分析新旧常态中国产业全碳足迹网络特征。经比较发现,构造的新旧常态中国产业全碳足迹复杂网络整体结构合理;较旧常态而言,新常态产业全碳足迹联系更为紧密,核心关键产业控制影响力更强,社团结构则总体保持稳定。在此基础上,提出综合衡量产业全碳足迹、全面顾及个体及整体特征、重点关注核心关键节点和充分考虑产业社团特征的对策建议,以求更有效提升新常态中国产业协同减排效率。     

复杂网络视角下世界石油流动的竞合态势演变及对中国石油合作的启示

世界石油流动的规模和复杂性日益增加,从复杂网络分析视角考察石油流动中主要贸易国及其所处地缘区之间的相对地位及变动,并分析中国在其中的竞合关系,有利于从与出口地缘区合作和与进口地缘区合作两个方面,全面审视中国石油合作的总体格局、重点合作国家和可能的模式创新。研究结果表明：（1）世界石油流动仍由主要出口地缘区主导,逐步演变为俄罗斯—中亚、美国—加拿大和中东三足鼎立的出口竞争格局,但出口地缘区的多元化和地位相对变动也为进口国调整合作关系提供了机遇;（2）亚太地区逐步成为世界石油流动的竞合焦点,但由于区内大国缺乏互济交流,降低了地区的整体核心地位和对石油流动的调控力,中国也深陷进口分散化、出口大国博弈和进口大国制衡三大困境中;（3）中国应与核心出口地缘区重点合作,与其他出口地缘区稳定合作并创新合作模式,与亚太其他进口国基于进口份额协调机制、来源错位竞争机制和国际贸易中心分工协作机制,开展区内互济交流合作,以改善中国在世界石油流动格局中的竞合环境,保障石油供需平衡、降低供给风险。     

双子型复配增强两性膨润土吸附Cr(VI)的效应

在两性修饰剂十二烷基二甲基甜菜碱（BS）修饰膨润土的基础上,采用双子型阳离子修饰剂乙撑基双十四烷基二甲基氯化铵（EB）对其进行复配修饰,以批处理法研究了不同修饰比例、温度、pH值和离子强度条件下,BS+EB复配修饰膨润土对Cr（VI）的吸附规律和热力学特征,并通过吸附Cr（VI）前后BS+EB复配修饰膨润土的红外光谱和表面电荷探讨了其吸附机制.结果表明,与BS两性修饰膨润土比较,EB复配修饰显著增强了其对Cr（VI）的吸附能力,吸附量增加了2.02~27.25倍,30℃时吸附量呈现BS+150EB（BS和150%比例的EB复配修饰膨润土） > BS+100EB > BS+50EB > BS+25EB > BS > CK（膨润土）的趋势,对Cr（VI）的吸附量随EB修饰比例增加而上升.CK、BS修饰膨润土对Cr（VI）呈现自发、熵增和焓增的特征,而BS+EB复配修饰膨润土对Cr（VI）吸附量随着温度的升高而降低,呈现出增温负效应.随着pH值的升高、离子强度增加,各供试土样对Cr（VI）的吸附量逐渐降低.红外光谱和土壤表面电荷结果证实电荷引力是BS+EB复配修饰土吸附Cr（VI）的主要机制.     

Mn2+促进载体挂膜的机理研究

通过向自制固定床生物膜反应器(FBBR)中投加氯化锰,考察了Mn~(2+)对生物膜量、形态结构、降解性能及其胞外聚合物(EPS)组分的影响,并探究了Mn~(2+)在生物膜形成中的作用、影响规律及其对生物膜反应器运行效能的影响.结果表明,投加Mn~(2+)有助于生物膜形成,增强生物膜致密性,并促进生物膜生长;在生物膜成熟期连续投加10 mg·L~(-1)Mn~(2+)对一个周期内生物膜的降解活性影响很小,反应器COD和NH_4~+去除率分别达到85.4%±1.5%和76.3%±1.9%;生物膜不同类型EPS含量的变化表明,Mn~(2+)不仅加速了生物膜的成熟和增强了生物膜去除有机物的稳定性,而且还会刺激生物膜分泌产生更多的紧密粘附型EPS,其中的蛋白质和多糖能够保护微生物免受Mn~(2+)伤害.     

山东省电力资源空间格局及环境成本分析

基于复杂网络理论,对山东省电力网络空间结构、分布特征进行了分析.结果发现：受资源禀赋的影响,山东省电力输出端主要分布在鲁西南地区,输入端主要集中在中东部重工业城市;电力网络拓扑结构具有较小的聚类系数和较大的平均路径长度,度分布呈现出不完全幂律分布,具有向无标度网络演化的特征;受电源结构的影响,各地市发电环境成本差异较大,尤其与火电发电规模紧密联系.     

Effect of iron ion configurations on Ni2+ removal in electrocoagulation

Electrocoagulation (EC) has been widely used to treat the heavy metal wastewater in industry. A novel process of sinusoidal alternating current electrocoagulation (SACC) is adopted to remove Ni²⁺ in wastewater in this study. The morphology of precipitates and the distribution of the main functional iron configurations were investigated. Ferron timed complex spectroscopy can identify the monomeric iron configurations [Fe(a)], oligomeric iron configurations [Fe(b)] and polymeric iron configurations [Fe(c)]. The optimal operating conditions of SACC process were determined through single-factor experiments. The maximum Ni²⁺ removal efficiency [Re(Ni²⁺)] was achieved under the conditions of pH₀=7, current density (j) = 7 A/m², electrolysis time (t) = 25 min, c₀(Ni²⁺) = 100 mg/L. At pH=7, the proportion of Fe(b) and Fe(c) in the system was 50.4 at.% and 23.1 at.%, respectively. In the SACC process, Fe(b) and Fe(c) are the main iron configurations in solution, while Fe(c) are the vast majority of the iron configurations in the direct current electrocoagulation (DCC) process. Re(Ni²⁺) is 99.56% for SACC and 98.75% for DCC under the same optimum conditions, respectively. The precipitates produced by SACC have a high proportion of Fe(b) configurations with spherical α-FeOOH and γ-FeOOH structures which contain abundant hydroxyl groups. Moreover, it is demonstrated that Fe(b) has better adsorption capacity than Fe(c) through adsorption experiments of methyl orange (MO) dye. Fe(a) configurations in the homogeneous solution had no effect on the removal of nickel.     

Solubility products of six metal‐glyphosate complexes in water and forestry soils,and their influence on glyphosate toxicity to plants

Abstract

The solubility products (K_sp) of 1:1 complexes of glyphosate, [N‐(phosphonomethyl)glycine], with Mg²⁺, Ca²⁺, Mn²⁺, Zn²⁺, Cu²⁺ and Fe³⁺, were determined in buffered (pH 7.0) distilled water, moist Ottawa sand, sandy loam and clay loam soils, each adjusted to 0.02 M with respect to KNO₃. The K_sp values decreased in the order of Mg ? Ca > Mn > Zn > Cu > Fe, regardless of the medium in which they were determined. The constants measured in Ottawa sand were similar to those in water, but those in the forestry soils depended upon the type of metal ion involved. The values for the Mg, Ca, Mn and Zn complexes were about 2 to 3 times lower in sandy loam soil than those in water, but those in clay loam were about 3 to 10 times lower. The K_sp of the Cu and Fe complexes were similar to those in water regardless of the soil type used.

In a bioassay experiment using tomato plants, immersed in the saturated solutions of the complexes or planted in the sand and soils containing saturated solutions of the complexes, no mortality occurred although slight inhibition in growth was observed in all cases. The most soluble complexes of Mg and Ca caused the most reduction in plant height, while the least soluble complex of Fe caused little growth inhibition. The Zn, Cu and Mn complexes caused some growth inhibition depending on their K_sp values. The larger the solubility product, the greater the concentration of glyphosate ion in solution, and the greater the growth inhibition. In a similar experiment using white spruce seedlings, growth inhibition was insignificant over the 12‐d bioassay period.