Stabilization of Cd-, Pb-, Cu- and Zn-contaminated calcareous agricultural soil using red mud: a field experiment

Red mud (RM) was used to remediate heavy metal-contaminated soils. Experiments with two different dosages of RM added to soils were carried out in this study. It was found that soil pH increased 0.3 and 0.5 unit with the dosage of 3 and 5% (wt%), respectively. At the dosage of 5%, the highest stabilization efficiencies for Cd, Pb, Cu and Zn reached 67.95, 64.21, 43.73 and 63.73%, respectively. The addition of RM obviously transferred Cd from the exchangeable fraction to the residual fraction. Meanwhile, in comparison with the control (no RM added), it reduced 24.38, 49.20, 19.42 and 8.89% of Cd, Pb, Cu and Zn in wheat grains at the RM addition dosage of 5%, respectively. At the same time, the yield of wheat grains increased 17.81 and 24.66% at the RM addition dosage of 3 and 5%, respectively. Finally, the addition of RM did not change the soil bacterial community. These results indicate that RM has a great potential in stabilizing heavy metals in calcareous agricultural soils.

     

The temporal changes of the concentration level of typical toxic organics in the river sediments around Beijing

In this study, the current situation of five types of toxic organics and endocrine disrupters in the sediments of rivers around Beijing, i.e., polycyclic aromatic hydrocarbons (PAHs), phthalic acid esters (PAEs), organic chlorinated pesticides (OCPs), estrogens (Es), and bisphenol A (BPA), which included 56 contaminants, was analyzed and compared with that registered by the historical literatures. The ecological risks were also assessed. The total concentration of PAHs, PAEs, OCPs, Es, and BPA ranged from 232.5 ng·g^–1 to 5429.7 ng·g^–1, 2047.2 ng·g^–1 to 18051.5 ng·g^–1, 4.5 ng·g^–1 to 11.7 ng·g^–1, 18.1 ng·g^–1 to 105.2 ng·g^–1, and 36.3 ng·g^–1 to 69.6 ng·g^–1, respectively. Among these five types of organic compounds, the concentration levels of PAHs and OCPs have decreased significantly in the last ten years, while those of PAEs and Es had an upward trend compared with the previous studies. BPA still remained at a moderately high level, as it was ten years ago. The risks of the PAEs in all of the sample sites, and fluoranthene, benzo[a]anthrene, and benzo[a]pyrene in the Wenyu River sediment, were relatively high. These results supplemented the database of toxic organics’ concentration levels in the sediments of Beijing rivers.

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Enhancement of extracellular Cr(VI) reduction for anammox recovery using hydrazine: performance,pathways, and mechanism

● N₂H₄ addition enhanced and recovered anammox performance under Cr(VI) stress. ● N₂H₄ accelerated electron transfer of Cr(VI) reduction for detoxification. ● N₂H₄ enhanced anammox metabolism for activity recovery from Cr(VI) inhibition. ● Extracellular Cr(VI) reduction to less toxic Cr(III) was the dominant mechanism. The hexavalent chromium (Cr(VI)) would frequently impose inhibition to anaerobic ammonium oxidation (anammox) process, hindering the efficiency of nitrogen removal in wastewater treatment. Hydrazine (N₂H₄), which is an intermediate product of anammox, participates in intracellular metabolism and extracellular Cr(VI) reduction. However, the roles of N₂H₄-induced intracellular metabolism and extracellular reduction in nitrogen removal under Cr(VI) stress remain unclear. The addition of 3.67 mg/L of N₂H₄ increased the anammox activity by 17%. As an intermediate, N₂H₄ enhanced anammox metabolism by increasing the heme c content and electron transfer system activity. As a reductant, N₂H₄ accelerated the reduction of c-Cyts-mediated extracellular Cr(VI) to the less toxic Cr(III). Extracellular Cr(III) accounts for 74% of the total Cr in a Cr(VI)-stressed anammox consortia. These findings highlight that N₂H₄-induced extracellular Cr(VI) reduction is the dominant mechanism for the survival of anammox consortia. We also found that N₂H₄ increased the production of extracellular polymeric substances to sequester excessive Cr(VI) and produced Cr(III). Taken together, the study findings suggest a potential strategy for enhancing nitrogen removal from ammonium-rich wastewater contaminated with Cr(VI).     

Removal of nitrogen from wastewaters by anaerobic ammonium oxidation (ANAMMOX) using granules in upflow reactors

Nitrogen pollution of waters has sometimes caused severe eutrophication, leading to the death of fishes and most aquatic life. There is therefore a need for efficient and cost-effective methods to remove nitrogen from ammonium-rich wastewaters. Anaerobic ammonium oxidation (ANAMMOX) is a promising process to remove nitrogen because this process directly oxidizes ammonium (NH₄ ⁺) to dinitrogen gas (N₂) under anoxic condition. Nonetheless, a challenge of this process is that chemolithoautotrophic Anammox bacteria grow slowly at the beginning, thus resulting in low Anammox biomass and instability of reactors. Such issues can be overcome by granulation of the Anammox sludge. Here, we review the characteristics of the Anammox bacteria, and the formation, structure and flotation of Anammox granules under high hydraulic loadings. We also evaluate the performances of full-scale granular Anammox processes. The major points are: 1) Anammox bacteria secrete a large amount of extracellular polymeric substances (EPS), up to 415 mg g^?1 of volatile suspended solids (VSS), containing many hydrophobic functional groups that facilitate biomass granulation. 2) Granulation enhances the sludge settling property and retention time, which contributes to the extremely high nitrogen removal rate of 77 kg m^?3 d^?1 of Anammox upflow reactors. 3) Flotation of Anammox granules frequently occurs under nitrogen removal rate higher than 10 kg m^?3 d^?1, which is mainly due to the overproduction of EPS under high hydraulic conditions.     

Effect of pH on the sonochemical degradation of organic pollutants

An increasing number of organic compounds are manufactured, consumed, and discarded every year. Incomplete destruction of these compounds in wastewater treatment plants leads to pollution of natural waters, posing great health and ecological concerns. Ultrasound, as an emerging advanced oxidation technology, can quickly and effectively degrade organic pollutants in waters. To improve removal efficiency of organic pollutants in an ultrasonic system, operational parameters, especially pH, have been frequently evaluated and optimized. This review show that pH-induced changes in volatility, hydrophobicity and Coulombic force between the target compound and cavitation bubbles leads to higher degradation at acidic pH for most compounds. In addition, pH also changes free radical formation and reactivity in water during sonication, thereby altering degradation kinetics of target compounds. However, the influence of pH is not always consistent for various organic pollutants covering a broad range of physicochemical properties and reactivities. A systematic investigation on the pH effect is necessary to elucidate how pH alters cavitation bubble dynamics and collapse, radical yield and reactivity, distribution of target compounds in the vicinity of cavitation bubbles, water matrices transformation, and ultimately the degradation kinetics of organic pollutants. This first systematic review provides valuable insight into the pH effects on organic pollutant sonolysis, helps to improve our mechanistic understanding of the sonochemical system, and sheds light on future application of ultrasound in water engineering.     

Red mud-modified biochar reduces soil arsenic availability and changes bacterial composition

Environmental Chemistry Letters - Worldwide arsenic (As) contamination in soils induces pollution of surface and ground waters, reduces crop quality and yield, and threatens human health....     

炭素焙烧炉沥青烟静电除尘技术

针对炭素焙烧炉含尘低浓度高温沥青烟，优化设计方案，采用干式、湿式预处理和静电净化两级处理，先除去大粒径烟尘，降低烟尘温度，降低电阻率，后静电净化沥青烟。系统具有自动控制，节电节能，除尘效率高等特点。     

Fe2O3添加对钛基SCR催化剂表面硫酸氢铵分解行为的影响规律

采用共沉淀法合成了TiO_2及TiO_2-Fe_2O_3载体,并对硫酸氢铵与上述载体之间的相互作用及硫酸氢铵的具体分解行为进行了研究.结果表明,催化剂载体表面含硫官能团主要以双齿硫酸盐的形式存在,含氮官能团以铵根离子的形式存在.当硫酸氢铵沉积于催化剂载体表面时,由于硫酸根离子具有较强的电负性,Ti原子及Fe原子处于电子缺失状态.对于TiO_2载体,硫酸根离子主要与Ti原子相连;而对于TiO_2-Fe_2O_3载体,Ti原子及Fe原子均为硫酸根离子主要的附着位点.采用热分析方法及原位红外对硫酸氢铵在TiO_2及TiO_2-Fe_2O_3载体表面的分解行为进行了研究,发现铁氧化物的添加显著促进了硫酸氢铵在低温区间内的分解行为;与铵根离子相比,硫酸根离子具有更高的热稳定性.催化剂稳定性测试结果表明,铁氧化物的添加显著提高了低温抗硫抗水性能,为实现低温SCR技术的工业应用提供了理论基础.     

低频振动对铀尾矿库滩面多层覆盖层控氡效果影响的研究

以湖南省某铀尾矿库为研究对象,基于自制的水平低频振动实验装置与铀尾矿库滩面缩尺模型,进行了水平单向低频振动研究,探究滩面多层覆盖层振动前后氡析出的规律.实验结果表明在单向振动4个频率条件及叠加振动4个频率条件下,模型表层随着频率的递增,裂隙逐步增大;当单一振动频率为25 Hz时,红土-石英砂-红土覆盖层振动后控氡率下降...     

Nitrogen nutrition in cotton and control strategies for greenhouse gas emissions: a review

Cotton (Gossypium hirustum L.) is grown globally as a major source of natural fiber. Nitrogen (N) management is cumbersome in cotton production systems; it has more impacts on yield, maturity, and lint quality of a cotton crop than other primary plant nutrient. Application and production of N fertilizers consume large amounts of energy, and excess application can cause environmental concerns, i.e., nitrate in ground water, and the production of nitrous oxide a highly potent greenhouse gas (GHG) to the atmosphere, which is a global concern. Therefore, improving nitrogen use efficiency (NUE) of cotton plant is critical in this context. Slow-release fertilizers (e.g., polymer-coated urea) have the potential to increase cotton yield and reduce environmental pollution due to more efficient use of nutrients. Limited literature is available on the mitigation of GHG emissions for cotton production. Therefore, this review focuses on the role of N fertilization, in cotton growth and GHG emission management strategies, and will assess, justify, and organize the researchable priorities. Nitrate and ammonium nitrogen are essential nutrients for successful crop production. Ammonia (NH₃) is a central intermediate in plant N metabolism. NH₃ is assimilated in cotton by the mediation of glutamine synthetase, glutamine (z-) oxoglutarate amino-transferase enzyme systems in two steps: the first step requires adenosine triphosphate (ATP) to add NH₃ to glutamate to form glutamine (Gln), and the second step transfers the NH₃ from glutamine (Gln) to α-ketoglutarate to form two glutamates. Once NH₃ has been incorporated into glutamate, it can be transferred to other carbon skeletons by various transaminases to form additional amino acids. The glutamate and glutamine formed can rapidly be used for the synthesis of low-molecular-weight organic N compounds (LMWONCs) such as amides, amino acids, ureides, amines, and peptides that are further synthesized into high-molecular-weight organic N compounds (HMWONCs) such as proteins and nucleic acids.