初论元素富集成矿的地球化学机理—以岩浆热液矿床的形成为例

元素富集成矿的过程实质上是元素在地球不同圈层和不同相以及不同集合体之间分配的结果。元素的富集起始于地球形成的初期。对于大多数金属成矿元素 ,地壳特别是上地壳是大多数矿石和矿胎的储库 ,地壳丰度是元素富集成矿的物质基础。元素在地质体系演化共存相间的分配是元素富集成矿的关键过程。对于以侵入体为中心的热液矿床的形成 ,岩浆部分熔融、结晶分异、液态分离、挥发分分离以及气液相不混溶等过程能够导致金属元素最终达到矿石级的富集。挥发分则是元素富集成矿的重要制约因素     

浙江墩头盆地横山组孢粉化石的发现及其地层意义

浙江墩头盆地红色岩层中上部首获丰富的以Cassopllis为主(58.39—62.54％)伴有Exesipollenites(15.21—15.84％),Hsuisporites(0.56—0.62％),Cicatricosisporites(0—0.31％)等孢粉化石。该孢粉组合特征既与国内外晚侏罗世孢粉组合面貌差别较大,又与早白垩世中晚期孢粉组合面貌存在明显差异,显示了早白垩世早期孢粉组合的色彩。笔者认为这套红色岩层应归早白垩世早期横山组为宜。     

Prediction of polychlorinated dibenzofuran congener distribution from gas-phase phenol condensation pathways

A model for predicting the distribution of dibenzofuran and polychlorinated dibenzofuran (PCDF) congeners from a distribution of phenols was developed. The model is based on a simplified chemical mechanism. Relative rate constants and reaction order with respect to phenol precursors were derived from experimental results using single phenols and equal molar mixtures of up to four phenols. For validation, experiments were performed at three temperatures using a distribution of phenol and 19 chlorinated phenols as measured in municipal waste incinerator exhaust gas. Comparison of experimental measurements and model predictions for PCDF isomer distributions and homologue pattern shows agreement within measurement uncertainty. The R-squared correlation coefficient exceeds 0.9 for all PCDF isomer distributions and the distribution of PCDF homologues. These results demonstrate that the distribution of dibenzofuran and the 135 PCDF congeners from gas-phase condensation of phenol and chlorinated phenols can be predicted from measurement of the distribution of phenol and the 19 chlorinated phenol congeners.     

石灰湿法脱硫过程中pH条件对结垢的影响研究

针对石灰湿法脱硫中存在的结垢问题，在鼓泡床中模拟了石灰湿法脱硫过程，通过分析液相的组成，结合反应机理探讨了pH对结垢的影响。结果表明，当pH控制在6.0～4．0时，既能避免结垢，又能获得较高的脱硫率。提出了实际中预测结垢倾向的方法。     

合肥市典型交通干道大气苯系物的特征分析

为研究合肥市交通干道大气苯系物污染状况,采用自主研制的差分吸收光谱(DOAS)系统,于2016年3月期间对合肥市交通主干道大气苯系物(苯、甲苯、间二甲苯和邻二甲苯)以及常规污染物NO_2、SO_2等进行了连续观测.观测结果显示,观测期间苯、甲苯、间二甲苯和邻二甲苯的平均浓度分别为:21.7、63.6、33.9和98.7μg·m~(-3).与国内外其它城市比较显示,合肥市交通干道大气苯和甲苯的污染处于中等水平,二甲苯的污染较为严重.结合观测期的间风速风向、T/B特征比值以及与CO等污染物的相关性,对上述苯系物来源进行了分析,结果显示观测期间T/B值为0.8~4.5,苯、甲苯与CO的相关性系数R分别为0.55和0.34.表明机动车尾气排放是观测区域苯和甲苯的主要排放源之一,同时也受到周边工业园区排放的影响,二甲苯的主要排放源为观测地点北偏东方向的涂料行业工业园区.苯和甲苯的夜间高浓度峰值分析结果表明,夜间的高浓度苯和甲苯可能主要来源于观测地点周边工业园区的排放.观测区域苯系物的臭氧生成潜势(OFP)表现为邻二甲苯间二甲苯甲苯苯,其中二甲苯的OFP占总OFP的85%,表明周边工业园区的排放对该地区臭氧生成的贡献较大.     

Simultaneous removal of ammonia and N-nitrosamine precursors from high ammonia water by zeolite and powdered activated carbon

When adding sufficient chlorine to achieve breakpoint chlorination to source water containing high concentration of ammonia during drinking water treatment, high concentrations of disinfection by-products(DBPs) may form. If N-nitrosamine precursors are present, highly toxic N-nitrosamines, primarily N-nitrosodimethylamine(NDMA), may also form. Removing their precursors before disinfection should be a more effective way to minimize these DBPs formation. In this study, zeolites and activated carbon were examined for ammonia and N-nitrosamine precursor removal when incorporated into drinking water treatment processes.The test results indicate that Mordenite zeolite can remove ammonia and five of seven N-nitrosamine precursors efficiently by single step adsorption test. The practical applicability was evaluated by simulation of typical drinking water treatment processes using six-gang stirring system. The Mordenite zeolite was applied at the steps of lime softening, alum coagulation, and alum coagulation with powdered activated carbon(PAC) sorption. While the lime softening process resulted in poor zeolite performance, alum coagulation did not impact ammonia and N-nitrosamine precursor removal. During alum coagulation, more than67% ammonia and 70%–100% N-nitrosamine precursors were removed by Mordenite zeolite(except 3-(dimethylaminomethyl)indole(DMAI) and 4-dimethylaminoantipyrine(DMAP)). PAC effectively removed DMAI and DMAP when added during alum coagulation. A combination of the zeolite and PAC selected efficiently removed ammonia and all tested seven N-nitrosamine precursors(dimethylamine(DMA), ethylmethylamine(EMA), diethylamine(DEA), dipropylamine(DPA), trimethylamine(TMA), DMAP, and DMAI) during the alum coagulation process.     

Characteristics of molecular weight distribution of dissolved organic matter in bromide-containing water and disinfection by-product formation properties during treatment processes

The characteristics of dissolved organic matter (DOM) and bromide ion concentration have a significant influence on the formation of disinfection by-products (DBPs). In order to identify the main DBP precursors, DOM was divided into five fractions based on molecular weight (MW), trihalomethane formation potential and haloacetic acid formation potential were determined for fractions, and the change in contents of different fractions and total DBPs during treatment processes (pre-chlorination, coagulation, sand filtration, disinfection) were studied. Moreover, the relationship between bromide concentration and DBP generation characteristics in processes was also analyzed. The results showed that the main DBP precursors were the fraction with MW < 1 kDa and fraction with MW 3−10 kDa, and the DBP''s generation ability of lower molecular weight DOM (< 10 kDa) was higher than that of higher molecular weight DOM. During different processes, pre-chlorination and disinfection had limited effect on removing organics but could alter the MW distribution, and coagulation and filtration could effectively remove organics with higher MW. For DBPs, trihalomethanes (THMs) were mainly generated in pre-chlorination and disinfection, while haloacetic acids (HAAs) were mostly generated during pre-chlorination; coagulation and sand filtration had little effect on THMs but resulted in a slight removal of HAAs. In addition, the results of ANOVA tests suggested that molecular sizes and treatment processes have significant influence on DBP formation. With increasing bromide concentration, the brominated DBPs significantly increased, but the bromine incorporation factor in the processes was basically consistent at each concentration.     

The fate of prazosin and levonorgestrel after electrochemical degradation process: Monitoring by-products using LC-TOF/MS

Prazosin (PRZ) and levonorgestrel (LNG) are widely used as an anti-disease drugs due to their biological activity in the human body. The frequent detection of these compounds in water samples requires alternative technologies for the removal of both compounds. After electrochemical degradation of PRZ and LNG, the parent compounds could be completely removed after treatment, but the identification and characterization of by-products are necessary as well. In this study, the effects of NaCl concentration and applied voltage were investigated during the electrochemical degradation process. The results revealed that the increase of NaCl concentration and applied voltage could promote the generation of hypochlorite OCl? and then enhance the degradation of PRZ and LNG. After initial study, 6 V and 0.2 g NaCl were selected for further experiments (96% and 99% removal of PRZ and LNG after 40 min, respectively). Energy consumption was also evaluated and calculated for PRZ and LNG at 3, 6 and 8 V. Solid phase extraction (SPE) method plays an important role in enhancing the detection limit of by-products. Furthermore, characterization and identification of chlorinated and non-chlorinated by-products were conducted using an accurate liquid chromatography-time of flight/mass spectrometry LC-TOF/MS instrument. The monitoring of products during the electrochemical degradation process was performed at 6 V and 0.2 g NaCl in a 50 mL solution. The results indicated that two chlorinated products were formed during the electrochemical process. The toxicity of by-products toward E. coli bacteria was investigated at 37°C and 20 hr incubation time.     

Impact of density of coating agent on antibacterial activity of silver nanoparticle impregnated plasma treated activated carbon

To use stabilized nanoparticles(NPs) in water as disinfectants over a very long period, the amount of coating agent(for NP stabilization) needs to be optimized. To this end, silver nanoparticles(Ag-NPs) with two different coating densities of tri-sodium citrate(12.05 and46.17 molecules/nm~2, respectively), yet of very similar particle size(29 and 27 nm, respectively)were synthesized. Both sets of citrate capped NPs were then separately impregnated on plasma treated activated carbon(AC), with similar Ag loading of 0.8 and 0.82 wt.%, respectively. On passing contaminated water(containing 10~4 CFU Escherichia coli/m L of water) through a continuous flow-column packed with Ag/AC, zero cell concentration was achieved in 22 and 39 min, with Ag-NPs(impregnated on AC, named as Ag/AC) having lower and higher coating density, respectively. Therefore, even on ensuring similar Ag-NP size and loading, there is a significant difference in antibacterial performance based on citrate coating density in Ag/AC.This is observed in lower coating density case, due to both:(i) higher Ag~+ ion release from Ag-NP and(ii) stronger binding of individual Ag-NPs on AC. The latter ensures that, Ag-NP does not detach from the AC surface for a long duration. TGA-DSC shows that Ag-NPs with a low coating density bind to AC with 4.55 times higher adsorption energy, compared to Ag/AC with a high coating density, implying stronger binding. Therefore, coating density is an important parameter for achieving higher antibacterial efficacy, translating into a faster decontamination rate in experiments, over a long period of flow-column operation.     

硫自养反硝化过程中含硫副产物产生规律及微生物群落结构的空间分布

为探究硫自养反硝化过程中含硫副产物的产生规律,建立了上流式硫自养固定床生物反应器,考察HRT（水力停留时间）对水中NO₃--N去除的影响,运用零级和1/2级反应动力学模型对NO₃--N还原过程进行拟合,通过测定与理论计算分析含硫副产物的产生趋势及规律,利用高通量测序技术（high-throughput sequencing）测定微生物群落结构空间分布特征.结果表明:①当进水NO₃--N浓度为（30.45±0.38）mg/L,HRT为4和1 h时,NO₃--N去除率达到98%以上.硫自养反硝化过程符合1/2级反应动力学模型,1/2K_1/2V（1/2级反应动力学速率常数）为5.69 mg1/2/（L1/2·h）.②出水SO₄2-的产生量接近理论值,S2-在反应器中部出现微量的积累,在出水口处浓度进一步降低（< 0.5 mg/L）.③HRT的缩短改变了反应器内部微生物群落α多样性的变化规律;Proteobacteria成为了最主要的优势菌群,各阶段所占比例均大于59%,Sulfurimonas为最常见的反硝化菌,在HRT为1 h时,反应器中部其丰度达到36%,成为反应器中的优势菌属;Desulfurella为SRB（硫酸盐还原菌）,其丰度的增加与反应器内部S2-的积累一致.研究显示,硫自养反硝化过程中产生的SO₄2-与理论值接近,S2-产生量沿反应器高度方向呈现先增加后降低的趋势,微生物群落结构分布情况与反应器高度有关.