Simultaneous carbon and nitrogen removal by anaerobic ammonium oxidation and denitrification under different operating strategies

Environmental Science and Pollution Research - Real domestic wastewater was treated initially in a sequencing batch reactor (SBR), with partial nitrification achieved before the effluent was used...     

养殖塘CH4通量时空变化特征及其影响因素

本研究基于多通道密闭式动态箱法对亚热带典型养殖塘CH₄通量的时空变化特征及其影响因素进行了分析.结果表明：亚热带养殖塘CH₄主要排放方式是冒泡,CH₄扩散及冒泡通量均呈现明显的季节变化特征.春、夏、秋、冬4个季节CH₄扩散通量分别为：0.113,0.830,0.002,0.005μmol/（m²·s）,冒泡通量分别为0.923,1.789,0.006,0.007μmol/（m²·s）,冒泡通量占总通量的比例分别为89.04%、68.29%、78.95%和60.52%.在冬、春季养殖塘没有人工管理措施的情况下,CH₄通量随着离岸距离的增加而增大,冬、春季养殖塘中间区域CH₄总通量分别是岸边浅水区的34.70和2.98倍.夏季养殖活跃期CH₄通量在空间上呈现出：人工投食区（7.371μmol/（m²·s））>自然生长区（2.151μmol/（m²·s））>人工增氧区（0.888μmol/（m²·s））>岸边浅水区（0.206μmol/（m²·s））的特征.在0.5h尺度上,春季CH₄扩散通量与水温呈显著正相关关系,与风速呈负相关关系,秋季CH₄扩散通量与水温、风速呈正相关关系,冒泡通量和水温呈正相关关系.在日尺度上,水温是CH₄扩散通量和冒泡通量的主控因子,两者均随着水温升高呈指数增加,并且冒泡通量的水温敏感性Q₁₀（12.72）大于扩散通量（7.78）.     

创新集聚空间分布模式对霾污染的影响

为了比较分析创新集聚空间分布单中心与多中心两种模式对霾污染的影响机制,本文构建了省域面板数据模型和中介效应模型进行实证检验.结果表明：创新集聚可通过规模效应降低霾污染;但创新集聚空间分布模式对霾污染的影响具有异质性.其中,单中心模式诱发了霾污染,存在创新集聚环境效应悖论;多中心模式对霾污染具有改善效应;随着创新集聚多中心的提高,其霾污染改善效应增强,但具有边际递减特征;能源利用效率是创新集聚空间分布模式影响霾污染的重要渠道之一.基于此,本文建议省级政府推进空间协同创新发展战略,建构省域多中心的创新网络空间组织体系,以此形成多中心协同治霾机制,破解创新集聚环境效应悖论.     

纳米单质铁对厌氧氨氧化脱氮性能的影响

通过向厌氧氨氧化反应器(ASBR)中投加纳米单质铁(nZVI),考察了其对厌氧氨氧化反应(ANAMMOX)脱氮性能的影响.结果表明,在温度为(25±0.5)℃,pH值为7.5±0.5,进水NH₄⁺-N和NO₂^--N浓度分别为30.35mg/L和37.89mg/L条件下,分别投加0,10,50,100.200,500,1000mg/L nZVI时,总氮去除率(NRE)分别达到70.27%、74.25%、83.45%、90.16%、68.59%、57.18%、50.93%.用修正的Boltzmann、Gompertz、Logistic模型对其进行动力学分析,R²值分别为0.9963、0.9944、0.9851,总氮(TN)出水浓度和NRE的预测值与实际值比较,其均方误差值分别为2.13、6.31、8.48和6.93、7.47、10.95.     

沙尘和灰霾期间中国近海大气氮沉降通量估算

利用WRF-CMAQ模型估算了2011年4月26日~5月3日沙尘事件和2016年1月1日~7日灰霾事件在中国近海引起的总无机氮（TIN）沉降通量,分析了两类事件对中国近海海洋初级生产力的贡献,探究了灰霾事件时中国近海无机氮沉降的可能来源.结果表明：典型沙尘和灰霾过程中,中国近海TIN干沉降通量均值分别为6.77,3.01mg N/（m²·d）,是晴朗天的6.84,3.04倍,可提供38.5,17.1mg C/（m²·d）的海洋初级生产力;沙尘期间无机氮沉降以还原态氮（NH₃和铵态氮,占TIN的62.2%）为主,灰霾期间则以氧化态氮（HNO₃和硝态氮,占TIN的84.3%）为主.典型沙尘事件TIN沉降对黄海影响最大,对渤海影响最小;典型灰霾事件对黄海和东海TIN沉降影响相当,高于对渤海的贡献.典型灰霾期间,京津冀和山东西北部（区域一）对渤、黄、东海TIN干沉降的贡献均大于长江三角洲及周边地区（区域二）,区域一对3个海域TIN干沉降的贡献约为38.7%~74.6%,区域二的贡献约为1.14%~12.1%.     

CeO2-ZrO2固溶体在催化湿式空气氧化苯酚废水中的作用

采用共沉淀法制备了CuO/ZnO/Ce O_2、CuO/ZnO/ZrO_2和CuO/ZnO/Ce O_2-Zr O_2催化湿式空气氧化苯酚废水催化剂,并采用N_2吸附-脱附、X射线衍射(XRD)、X射线光电子能谱(XPS)、程序升温还原(TPR)、N_2O滴定和电感耦合等离子体原子发射光谱等手段对催化剂进行了表征.结果表明,CuO/ZnO/Ce O_2-Zr O_2催化剂表现出最佳的催化性能.在200℃、2 MPa空气、苯酚初始浓度500 mg·L~(-1)的条件下,COD去除率为96.5%.XRD表明Ce O_2-Zr O_2复合氧化物载体以Ce_xZr_(1-x)O_2固溶体形式存在,增加了催化材料的储放氧能力.XPS表明Ce~(3+)和Ce~(4+)在催化剂表面共同存在,协调了氧化还原过程.TPR表明催化剂的还原性对催化剂的氧化活性起到至关重要的影响.由于CuO/ZnO/Ce O_2-Zr O_2催化剂活性组分和载体间的强相互作用,处理后的水样未发现金属离子,进而有效的提高了催化剂的稳定性和避免了对水样的二次污染.     

Reuse of Fenton sludge as an iron source for NiFe2O4 synthesis and its application in the Fenton-based process

The potentially hazardous iron-containing sludge from the Fenton process requires proper treatment and disposal, which often results in high treatment cost. In this study, a novel method for the reuse of Fenton sludge as an iron source for the synthesis of nickel ferrite particles(NiFe_2O_4) is proposed. Through a co-precipitation method followed by sintering at 800°C, magnetic NiFe_2O_4 particles were successfully synthesized, which was confirmed by powder X-ray diffraction(XRD), scanning electronic microscopy(SEM), energy dispersive spectroscopy(EDS), Fourier transform infrared spectroscopy(FT-IR) and Raman spectroscopy. The synthesized NiFe_2O_4 could be used as an efficient catalyst in the heterogeneous Fenton process. In phenol degradation with H_2O_2 or NiFe_2O_4 alone, the phenol removal efficiencies within the reaction time of 330 min were as low as 5.9% ± 0.1% and 13.5% ±0.4%, respectively. However, in the presence of both NiFe_2O_4 and H_2O_2, phenol removal efficiency as high as 95% ± 3.4% could be achieved, indicating the excellent catalytic performance of NiFe_2O_4 in the heterogeneous Fenton process. Notably, a rapid electron exchange between_Ni II and_Fe III ions in the NiFe_2O_4 structure could be beneficial for the Fenton reaction. In addition, the magnetic catalyst was relatively stable, highly active and recoverable, and has potential applications in the Fenton process for organic pollutant removal.     

Influences of LaCl3 on the mineral phase transformation during osteoblast mineralization in vitro

Rat calvarial osteoblasts were treated with lanthanum chloride (LaCl₃) to explore its effect on the mineral crystalline phase during the process of osteoblast calcification in vitro. The results confirmed that La was readily deposited in the mineral component of the matrix. Employing high-resolution transmission electron microscopy and Fourier transform infrared microspectroscopy techniques, we demonstrated that features comparable to dicalcium phosphate dihydrate (DCPD) and octacalcium phosphate, and hydroxyapatite (HAP) were detected in the mineral phases in vitro. Particularly, LaCl₃ treatment retarded conversion from DCPD-like phase into HAP during mineralization. In addition, La was introduced in DCPD powder during wet chemical synthesis. When compared with that of La-free DCPD, the dissolution rate of La-incorporated DCPD was lower, thereby leading to a delayed DCPD-to-HAP phase transformation. Thus, it can be concluded that LaCl₃ treatment influences the kinetics of inorganic phase transition by decreasing the dissolution rate of DCPD.     

陕西潼关冶金污染土壤的修复评价及应用潜力

为了科学评估客土法、石灰和磷酸钙作为重金属钝化剂的原位稳定化修复技术在实际重金属污染土壤改良中的应用潜力,以潼关县安乐乡土壤重金属污染修复示范工程为例,从"三小"冶金土壤污染现状、工程修复技术的筛选、稳定化的修复效果以及修复后土壤农业生产安全性评价等角度进行了系统分析.结果表明"三小"冶炼行为对于周边土壤造成了严重的污染,主要污染物为Cd、Pb和Hg,矿渣是主要的污染源.采用潜在生态危害指数法进行评价,该区域潜在生态危害指数(RI)范围为668~10 969,具有很强的生态危害.通过对重度污染和轻度污染土壤分别采用客土法及原位固化的修复方法,土壤中重金属的总量以及有效态含量均有了显著的下降.除Cd外,土壤中重金属的总量均低于土壤二级标准中的限值.尽管土壤稳定化修复取得了一定的效果,但部分农作物中重金属的累积量高于国家食品安全标准中规定的限值,继续种植存在一定的风险.因此,在重金属污染修复后的土壤上不建议立刻进行粮食生产,应改变原有生产模式同时持续监测,在确保粮食安全后再进行生产.