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1.
膨润土负载纳米铁去除地下水中六价铬研究 总被引:3,自引:1,他引:3
随着人民生活水平的提高和城市化进程的加快,有机污染物及重金属高强度场地污染对人类健康、生态环境及社会安全构成了严重威胁。地下水中的重金属Cr(Ⅵ)污染逐渐受到重视,纳米零价铁可以有效地将六价铬还原成三价铬,使其沉淀固定下来,从而将污染源区的污染物消减固定,防止其向周围扩散。然而由于纳米铁颗粒微小,易被氧化,极易团聚,自身活性受到限制,因此,纳米铁的分散性、稳定性、良好活性研究至关重要。采用低成本环境友好型粘土矿膨润土作为负载材料制备膨润土负载纳米铁(B-NZVI),批实验和柱实验研究B NZVI去除模拟地下水中Cr(Ⅵ)。结果表明:(1)自制的膨润土负载纳米铁个体呈球形,呈分散状负载于膨润土;(2)相同铁含量的B-NZVI处理Cr(Ⅵ)的效率远大于纳米铁,还原反应符合伪一级反应动力学模型,表观速率常数K随着B NZVI初始浓度的减小而减小;(3)B NZVI在石英砂柱中基本无迁移,适用于点源污染,Cr(Ⅵ)穿透曲线为B-NZVI的实际应用提供了理论和实验基础。 相似文献
2.
François Farges 《Physics and Chemistry of Minerals》2009,36(8):463-481
Cr K-edge XANES spectra were obtained for a variety of Cr-bearing model compounds containing Cr(II), Cr(III), Cr(IV), Cr(V) and Cr(VI), in which the Cr-site symmetry is D4h, Oh and Td. The centroid position of the pre-edge feature is a better indicator of the Cr valence than the edge position. In Cr-rich oxides, higher-energy transitions must be excluded in order to refine a robust valence for Cr. The pre-edge for chromates is not unique and varies as a function of the CrO4 2? moiety distortion, which is often related to Cr-polymerization (monochromate vs. dichromate). Both the analogy with the Mn K-pre-edge information and ab initio FEFF calculations of the pre-edge feature for Cr(III) and Cr(VI) confirm the experimental trends. This methodology is applied to the Cr K-edge pre-edge feature collected in gems (emerald, spinel and ruby), the layered minerals fuchsite and kämmererite, two Cr-bearing aqueous solutions and a set of sodo-calcic silicate glasses used for bottling sparkling white wine. In emerald and fuchsite, the Cr-site is differently distorted than its ruby or spinel counterpart. In a Cr(III)-bearing aqueous solution and sodo-calcic glass, no evidence for Cr(III) with Td and C3v symmetry is detected. However, minor amounts of chromate moieties (most likely monomeric) are detected in a glass synthesized in air. Preliminary spectra for the wine bottle glass suggest that only trace amounts of chromates might possibly be present in these glasses. 相似文献
3.
4.
乳化植物油强化土著微生物修复中高浓度Cr(Ⅵ)污染地下水 总被引:2,自引:0,他引:2
以天然细砂为微生物来源,模拟研究了乳化植物油强化原位生物修复中高浓度Cr(Ⅵ)污染地下水的可行性,考察了修复效果及修复过程中地下水质变化及产物的稳定性。结果表明,反应77 d后,Cr(Ⅵ)质量浓度分别从20.0、30.0、50.0、80.0、110.0 mg/L降低到0.0、5.8、19.0、43.6、65.8 mg/L,去除率分别为100.0%、80.7%、61.9%、45.5%、40.2%。反应后介质中Cr形态分析表明,其主要以能在自然条件下稳定存在的铁锰结合态和有机结合态形式存在。此外,随反应进行,实验体系逐渐呈弱酸性环境,pH为5.80~6.70。当Cr被完全还原后,体系会发生异化铁还原,Fe(Ⅱ)质量浓度逐渐升高,最高可达117.0 mg/L,最终形成二价铁矿物。综上所述,天然细砂介质中的土著微生物能够利用乳化植物油强化并还原地下水中的中、高浓度Cr(Ⅵ),且产物能够在自然状态下稳定存在,修复过程对地下环境的影响较小。 相似文献
5.
渗透反应格栅(permeable reactive barrier,PRB)在国外被广泛应用于场地尺度的地下水污染修复,因其无须外源动力、不占地面空间、运行成本低等优势在国内受到广泛关注。不同场地水文地质条件、污染物类型、污染羽分布具有差异性,前期场地调查、反应材料的筛选、反应墙尺寸结构的设计对于PRB的有效运行至关重要。本文以PRB修复河南某Cr(Ⅵ)污染场地为例,详细阐述场地调查、材料筛选、材料反应参数确定、PRB结构优化等方面的研究过程及成果,可为后续PRB修复技术的应用提供参考。研究结果表明:PRB修复技术适用于该场地,铸铁与活性炭混合材料为最佳修复材料;反应门长40 m(反应材料厚2 m,上下游分别为2 m厚砾石层),东西两侧隔水墙长为60 m的U型漏斗-门系统型PRB,可有效捕获并修复污染羽,工程成本远低于连续反应墙式PRB,为该场地修复最优PRB结构类型。 相似文献
6.
QIU Tian YANG Jingsui MILUSHI Ibrahim WU Weiwei MEKSHIQI Nezir XIONG Fahui ZHANG Cong SHEN Tingting 《《地质学报》英文版》2018,92(3):1063-1081
The Bulqiza ultramafic massif, which is part of the eastern Mirdita ophiolite of northern Albania, is world renowned for its high-Cr chromitite deposits. High-Cr chromitites hosted in the mantle section are the crystallized products of boninitic melts in a supra-subduction zone (SSZ). However, economically important high-Al chromitites are also present in massive dunite of the mantle-crust transition zone (MTZ). Chromian-spinel in the high-Al chromitites and dunites of the MTZ have much lower Cr# values (100Cr/(Cr+Al)) (47.7–55.1 and 46.5–51.7, respectively) than those in the high-Cr chromitites (78.2–80.4), harzburgites (72.6–77.9) and mantle dunites (79.4–84.3). The chemical differences in these two types of chromitites are reflected in the behaviors of their platinum-group elements (PGE). The high-Cr chromitites are rich in IPGE relative to PPGE with 0.10–0.45 PPGE/IPGE ratios, whereas the high-Al chromitites have relatively higher PPGE/IPGE ratios between 1.20 and 7.80. The calculated melts in equilibrium with the high-Cr chromitites are boninitic-like, and those associated with the high-Al chromitites are MORB-like but with hydrous, oxidized and TiO2-poor features. We propose that the coexistence of both types of chromitites in the Bulqiza ultramafic massif may indicates a change in magma composition from MORB-like to boninitic-like in a proto-forearc setting during subduction initiation. 相似文献
7.
During the manufacturing of chromate salts (1972–1992) large quantities of Chromite Ore Processing Residue (COPR) were released
into a decantation pond east of the former chemical plant of Porto-Romano (Durres, Albania), giving rise to yellow colored
pond sediments. These Cr(VI) bearing sediments were deposited upon Quaternary silty-clay lagoonal sediments rich in iron oxides
and organic matter. The pH values in these lagoonal sediments vary around 6.6, while in the pond sediments, it is mainly acidic
(due to the presence of the sulfur stock piles in the area and the release of the H2SO4 from the activity of the former chemical plant), varying between 1.4 and 3.8. Continuous leaching of the COPR waste resulted
in yellow-colored surface water runoff. The prediction of pH changes in the different types of sediments based upon acid/base
neutralizing capacity (ANC/BNC) jointly with the quantitative data on release of heavy metals and especially Cr is considered
an important advantage of the pHstat leaching test if compared to conventional leaching procedures. Thus, factors controlling the leaching of Cr(VI), Cr(III),
Ca, Al, Fe, Mg from the COPR were investigated by means of pHstat batch leaching tests and mineralogical analysis. Moreover, mathematical and geochemical modeling complemented the study.
The COPR in the area contain very high concentrations of chromium 24,409 mg/kg, which mainly occurs as Cr(III) (75–90%) as
well as Cr(VI) (25–10%). The leaching of Cr(VI) occurs in all the range (2–10) of the tested pH values, however, it decreases
under acidic conditions. Beside some reduction of Cr(VI) to Cr(III), the Cr(VI) content of the leachtes remains relatively
high in the acidic environment, while the limning of Cr(VI) pond sediments will increase the release of the latter specie.
The leaching of the Cr(III) occurs strictly under acidic conditions, whereby limning of these sediments will give rise to
the lower solubility of Cr(III). The key mineral phases responsible for the fast release of the Cr(VI) are: the chromate salts
(i.e. sodium chromate and sodium dichromate), while sparingly soluble chromatite (CaCrO4) and hashemite (BaCrO4) release Cr(VI) very slowly. Thus, pH and mineral solubility have been identified as key factors in the retention and the
release of the hexavalent CrO4
2− and Cr2O7
− from the COPR-rich pond sediments. 相似文献
8.
9.
Transformation of ammonium nitrogen and response characteristics of nitrifying functional genes in tannery sludge contaminated soil 下载免费PDF全文
Kong Xiang-ke Zhang Zi-xuan Wang Ping Wang Yan-yan Zhang Zhao-ji Han Zhan-tao Ma Li-sha 《地下水科学与工程》2022,10(3):223-232
High concentrations of ammonium nitrogen released from tannery sludge during storage in open air may cause nitrogen pollution to soil and groundwater. To study the transformation mechanism of NH4+-N by nitrifying functional bacteria in tannery sludge contaminated soils, a series of contaminated soil culture experiments were conducted in this study. The contents of ammonium nitrogen (as NH4+-N), nitrite nitrogen (as NO2?-N) and nitrate nitrogen (as NO3?-N) were analyzed during the culture period under different conditions of pollution load, soil particle and redox environment. Sigmodial equation was used to interpret the change of NO3?-N with time in contaminated soils. The abundance variations of nitrifying functional genes (amoA and nxrA) were also detected using the real-time quantitative fluorescence PCR method. The results show that the nitrification of NH4+-N was aggravated in the contaminated silt soil and fine sand under the condition of lower pollution load, finer particle size and more oxidizing environment. The sigmodial equation well fitted the dynamic accumulation curve of the NO3?-N content in the tannery sludge contaminated soils. The Cr(III) content increased with increasing pollution load, which inhibited the reproduction and activity of nitrifying bacteria in the soils, especially in coarse-grained soil. The accumulation of NO2?-N contents became more obvious with the increase of pollution load in the fine sand, and only 41.5% of the NH4+-N was transformed to NO3?-N. The redox environment was the main factor affecting nitrification process in the soil. Compared to the aerobic soil environment, the transformation of NH4+-N was significantly inhibited under anaerobic incubation condition, and the NO3?-N contents decreased by 37.2%, 61.9% and 91.9% under low, medium and high pollution loads, respectively. Nitrification was stronger in the silt soil since its copy number of amoA and nxrA genes was two times larger than that of fine sand. Moreover, the copy numbers of amoA and nxrA genes in the silt soil under the aerobic environment were 2.7 times and 2.2 times larger than those in the anaerobic environment. The abundance changes of the amoA and nxrA functional genes have a positive correlation with the nitrification intensity in the tannery sludge-contaminated soil. 相似文献
10.
The position of the transition from spinel peridotite to garnet peridotite in a simplified chemical composition has been determined experimentally at high pressures and high temperatures. The univariant reaction MgCr2O4+2Mg2Si2O6=Mg3Cr2Si3O12+Mg2SiO4, has a negative slope in P–T space between 1200 °C and 1600 °C. The experimental results, combined with assessed thermodynamic data for MgCr2O4, MgSiO3 and Mg2SiO4 give the entropy and enthalpy of formation of knorringite garnet (Mg3Cr2Si3O12). Thermodynamic calculations in simplified chemical compositions indicate that Cr shifts the garnet-in reaction to much higher pressures than previously anticipated. Moreover, in Cr-bearing systems a pressure–temperature field exists where garnet and spinel coexist. The width of this divariant field strongly depends on the Cr/(Cr+Al) of the system. 相似文献