混凝-催化氧化处理含油污水实验研究

采用复合化学混凝及催化氧化联合工艺对油田生产废水进行了实验研究.结果表明:含油废水经混凝处理后,剩余ρ(CODcr )可以达到300 mg/L左右,剩余悬浮物质量浓度小于10mg/L;再经活性炭载Cu、Pd催化剂的深度处理,含油污水中的ρ(CODcr )值由315 mg/L降至50 mg/L以下,达到了国家的相关排放标准.催化剂可以再生重复使用.     

糠醛废水处理工程实例

系统地阐述了用UASB厌氧生物处理糠醛废水技术的处理工艺,控制温度、pH值、营养盐的工艺条件,使糠醛废水经厌氧及生物接触氧化二级生物处理,可以稳定达到国家排放标准.     

Lepidocrocite-catalyzed Mn(II) oxygenation by air and its effect on the oxidation and mobilization of As(III)

Manganese (oxy)hydroxides (MnO_X) play important roles in the oxidation and mobilization of toxic As(III) in natural environments. Abiotic oxidation of Mn(II) to MnO_X in the presence of Fe minerals has been proved to be an important pathway in the formation of Mn(III, IV) (oxy)hydroxides. However, interactions between Mn(II) and As(III) in the presence of Fe minerals are still poorly understood. In this study, abiotic oxidation of Mn(II) on lepidocrocite, and its effect on the oxidation and mobilization of As(III) were investigated. The results show that MnO_X species are detected on lepidocrocite and their contents increase with increasing pH values ranging from 7.5 to 8.4. After 10 days, an MnOx component, groutite (α-MnOOH) was found on lepidocrocite. During the simultaneous oxidation of Mn(II) and As(III), and the As(III) pre-adsorbed processes, the presence and oxidation of Mn(II) significantly promotes the removal of soluble As(III). In addition, MnOx formed on lepidocrocite also contributes to the oxidation of soluble and adsorbed As(III) to As(V), the latter being subsequently released into solution. In the process where Mn(II) is pre-adsorbed on lepidocrocite, less As(III) is removed, given that the active sites occupied by MnOx inhibit the adsorption of As(III). In all experiments, the removal percentages of As(III) and the release of As(V) are correlated positively with pH values and initial concentrations of Mn(II), although they are not apparent in the Mn(II) pre-adsorbed system.     

鄂尔多斯盆地鄂托克前旗地区层间氧化带砂岩型铀矿成矿条件分析

本文通过对鄂尔多斯盆地鄂托克前旗地区区域地质概况、找矿目的层下白垩统志丹群华池 环河组地层岩性岩相和层间氧化带发育特征以及层间氧化带砂岩型铀矿化特征的研究, 综合分析了该区层间氧化带砂岩型铀矿成矿条件, 认为该区具有较好的铀成矿环境和找矿前景。     

Calculated phase equilibria for a morb composition in a P–T range, 450–650 °C and 18–28 kbar: the stability of eclogite

Lower temperature eclogite (with T = 600 °C) represents a significant part of the occurrences of eclogite in orogenic belts. ‘True’ eclogite, with, for example, garnet + omphacite >70%, is well represented in such an occurrence. Calculated phase equilibria in Na₂O–CaO–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O–TiO₂–O (NCKFMASHTO), for just one rock composition – that of a representative mid‐ocean ridge basalt, morb – are used to see under what circumstances ‘true’ eclogite is predicted to occur. The variables considered are not only pressure (P) and temperature (T) but also water content and oxidation state. The latter two variables are known to exert a significant control on mineral assemblage but are difficult to establish retrospectively from the observed rocks themselves. It is found that whereas oxidation state does have a strong effect on mineral assemblage, the key control on developing ‘true’ eclogite is shown to be temperature and water content. If temperature is established to be <600 °C, water content has to be low (less or much less than that for H₂O saturation) in order for ‘true’ eclogite to form. Moreover, unless pressure is at the high end in the range considered, lawsonite eclogite and ‘true’ eclogite will tend to be mutually exclusive, with the former requiring high water content at the lower temperature where it occurs, but the latter requiring low water content.     

Ephemeral acid mine drainage at the Montalbion silver mine,north Queensland

Sulfide‐rich materials comprising the waste at the abandoned Montalbion silver mine have undergone extensive oxidation prior to and after mining. Weathering has led to the development of an abundant and varied secondary mineral assemblage throughout the waste material. Post‐mining minerals are dominantly metal and/or alkali (hydrous) sulfates, and generally occur as earthy encrustations or floury dustings on the surface of other mineral grains. The variable solubility of these efflorescences combined with the irregular rainfall controls the chemistry of seepage waters emanating from the waste dumps. Irregular rainfall events dissolve the soluble efflorescences that have built up during dry periods, resulting in ‘first‐flush’ acid (pH 2.6–3.8) waters with elevated sulfate, Fe, Cu and Zn contents. Less‐soluble efflorescences, such as anglesite and plumbojarosite, retain Pb in the waste dump. Metal‐rich (Al, Cd, Co, Cu, Fe, Mn, Ni, Zn) acid mine drainage waters enter the local creek system. Oxygenation and hydrolysis of Fe lead to the formation of Fe‐rich precipitates (schwertmannite, goethite, amorphous Fe compounds) that, through adsorption and coprecipitation, preferentially incorporate As, Sb and In. Furthermore, during dry periods, evaporative precipitation of hydrous alkali and metal sulfate efflorescences occurs on the perimeter of stagnant pools. Flushing of the streambed by neutral pH waters during heavy rainfall events dissolves the efflorescences resulting in remobilisation and transport of sulfate and metals (particularly Cd, Zn) downstream. Thus, in areas of seasonal or irregular rainfall, secondary efflorescent minerals present in waste materials or drainage channels have an important influence on the chemistry of surface waters.     

接触变质作用对煤基石墨烯量子点的影响研究

为研究煤的接触变质作用对煤基石墨烯量子点性质的影响,以形成于深成变质、区域岩浆变质的煤为对比,采用氧化剥离法进行煤基石墨烯量子点的制备,并利用X射线衍射（XRD）、拉曼光谱（Raman）、透射电镜（TEM）、X射线光电子能谱（XPS）、荧光光谱（PL）对原煤及制备产物的结构进行分析。实验结果表明,随煤级升高,脱灰煤的结构缺陷减少,芳香片层逐渐增大,晶体结构向有序化方向进行。以煤为碳源制备而成的量子点,粒度均一性良好,并随煤级升高粒径有更大的趋势。碳元素以 C—C/C—H 形式为主,氧主要存在于碳氧官能团中,C∶O≤7∶3,且氧含量随煤级升高而升高。在紫外光（λ=297 nm）的照射下,样品散发蓝色荧光,且在煤级较低时荧光强度较大,并随煤级升高逐渐降低。相较于深成变质、区域岩浆变质形成的煤,接触变质作用形成的煤,产物具有更多的 COO— 结构,而 C==O 键含量降低;荧光强度在煤级较低时的上升趋势更为明显,并在高阶烟煤达到最大;受接触变质作用影响的煤,具有更加规则的石墨化结构。     

预处理／复合水解酸化／复合好氧氧化工艺处理综合制药废水

针对传统水解酸化和好氧氧化处理工艺存在的问题,对水解酸化工艺及好氧氧化处理工艺进行了改进;并针对东北制药集团制药废水水质特征,设计开发了预处理 复合水解酸化 复合好氧氧化的生物处理技术。工程设计规模为30000 m3/d,两年的运行结果表明,此工艺运行稳定,耐冲击负荷能力强。当平均进水浓度COD为3600 mg/L、BOD5为1000 mg/L、SS为450 mg/L时,平均出水浓度COD≤300mg/L、BOD5≤100 mg/L、SS≤50 mg/L,达到了国家城市排水三级标准医药企业污水排放标准(COD300mg/L)。     

Microbial Mats in the Mesoproterozoic Carbonates of the North China Platform and Their Potential for Hydrocarbon Generation

The well-preserved Mesoproterozoic succession in the North China platform consists mainly of three llthological associations including peritidal quartz sandstone, shallow marine and lagoonai dark to black shales, and shallow epeiric carbonates, with a total thickness of up to 8 000 m. In addition to well-documented microplants, macroalgae, and microbial buildups, abundant microbially induced sedimentary structures (MISS) and mat-related sediments have been recognized in these rocks. Intensive microbial mat layers and MISS are especially well preserved in the carbonates of the upper Gaoyuzhuang (高于庄) (ca. 1.5 Ga) and lower Wumishan (雾迷山) (ca. 1.45 Ga) formations, Indicating diversified microbial activities and a high organic production. In these petrified blomats, putative microbial fossils (both coccoidal and filamentous) and framboidal pyrites have been identified. The abundance of authigenic carbonate minerals in the host rocks, such as, acicular aragnnites, rosette barites, radial siderites, ankerites, and botryoidai carbonate cements, suggests authigenlc carbonate precipitation from anaerobic oxidation of methane (AOM) under anoxic/euxinic conditions. Warm climate and anoxic/euxinic conditions in the Mesoproterozoic oceans may have facilitated high microbial productivity and organic burial in sediments. Although authigenic carbonate cements may record carbonate precipitation from anaerobic methane oxidation, gas blister (or dome) structures may indicate gas release from active methanogenesls during shallow burial Bituminous fragments in mat-related carbonates also provide evidence for hydrocarbon generation. Under proper conditions, the Mesoproterozoic mat-rich carbonates will have the potential for hydrocarbon generation and serve as source rocks. On the basis of petrified biomats, a rough estimation suggests that the Mesoproterozoic carbonates of the North China platform might have a hydrocarbon production potential in theorder of 10×108t.     

Influence of extractable soil manganese on oxidation capacity of different soils in Korea

We examined the relationship between soil oxidation capacity and extractable soil manganese, iron oxides, and other soil properties. The Korean soils examined in this study exhibited low to medium Cr oxidation capacities, oxidizing 0.00–0.47 mmol/kg, except for TG-4 soils, which had the highest capacity for oxidizing added Cr(III) [>1.01 mmol/kg of oxidized Cr(VI)]. TG and US soils, with high Mn contents, had relatively high oxidation capacities. The Mn amounts extracted by dithionite-citrate-bicarbonate (DCB) (Mn^d), NH₂OH·HCl (Mn^h), and hydroquinone (Mn^r) were generally very similar, except for the YS1 soils, and were well correlated. Only small proportions of either total Mn or DCB-extractable Mn were extracted by NH₂OH·HCl and hydroquinone in the YS1 soils, suggesting inclusion of NH₂OH·HCl and hydroquinone-resistant Mn oxides, because these extractants are weaker reductants than DCB. No Cr oxidation test results were closely related to total Mn concentrations, but Mn^d, Mn^h, and Mn^r showed a relatively high correlation with the Cr tests (r = 0.655–0.851; P < 0.01). The concentrations of Mn^d and Mn^h were better correlated with the Cr oxidation tests than was the Mn^r concentration, suggesting that the oxidation capacity of our soil samples can be better explained by Mn^d and Mn^h than by Mn^r. The first component in principal components analysis indicated that extractable soil Mn was a main factor controlling net Cr oxidation in the soils. Total soil Mn, Fe oxides, and the clay fraction are crucial for predicting the mobility of pollutants and heavy metals in soils. The second principal component indicated that the presence of Fe oxides in soils had a significant relationship with the clay fraction and total Mn oxide, and was also related to heavy-metal concentrations (Zn, Cd, and Cu, but not Pb).