负载镍锌氧体木质素基活性炭吸附磺胺噻唑

以碱木素为原料热解制备碱木素基活性炭（LAC）,在此基础上添加硝酸镍、硝酸锌等,用水热合成法成功制备出负载镍锌氧体的木质素基活性炭（NiZn-DO/LAC）.通过SEM、BET、XRD等仪器对木质素基活性炭性能结构进行表征,并研究其在水溶液中对于磺胺噻唑（ST）的吸附.结果表明,所制得的木质素基活性炭具有明显的三维多孔结构与稳定的晶体结构,其具备较大的比表面积（759.1m²/g）.在吸附ST的过程中,NiZn-DO/LAC表现出较好的吸附性能,最大吸附容量可达328.2mg/g,优于其他报道的吸附剂.在NaOH溶液中,ST易从活性炭材料中脱附,在循环利用4次后,解吸率仍可达79.43%.NiZn-DO/LAC对ST的吸附主要通过静电作用、π-π堆积作用、络合作用、氢键作用及疏水性作用的协同,从而使吸附性能得到很大提高.     

污泥热水解滤液作污水反硝化碳源的脱氮性能

以污泥热水解滤液作为外加碳源,通过对SBR反应器脱氮效果、碳氮平衡及活性污泥EPS的分析,探究了污泥热水解滤液的脱氮性能,并与传统碳源乙酸钠进行了比较.结果表明,污泥热水解滤液和乙酸钠作为碳源可将出水TN从27.64mg/L分别降至12.05mg/L和7.98mg/L,说明两种碳源的投加均能强化反硝化过程;通过碳氮平衡分析可以看出,未加入碳源时污水TN去除率只有47.83%,加入热水解滤液后污水的TN去除率达到了81.30%,且滤液增加的氮负荷远远小于滤液作为外加碳源去除污水中TN的量;加入热水解滤液和乙酸钠时,活性污泥的EPS均有增加,但乙酸钠为碳源时的EPS含量更高,而EPS的增加引起了污泥SVI的增大.     

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）.     

雨洪管理措施的水环境效应差异——基于Meta的中国案例分析

雨洪管理措施的应用可有效控制雨水径流量及其污染物,系统分析雨洪管理措施对径流及其污染物的影响有助于理解雨洪管理的水环境效应。本文基于Meta方法整理国内已发表的文献案例,通过提取雨洪管理措施的类型、应用尺度、降雨特征及径流量和污染物削减率等信息,综述了雨洪管理措施应用后径流量和污染物的变化。结果表明：（1）不同雨洪管理措施所产生的水环境效应存在差异,样本中屋顶绿化的径流削减能力最强,透水铺装的径流污染物削减效果最佳;（2）雨洪管理措施对水环境的影响具有尺度效应,大尺度区域内雨洪管理措施对径流量削减作用较弱,而小尺度区域内径流污染物削减作用较弱;（3）雨洪管理措施对径流量及其污染物的削减能力随降雨量增加呈下降趋势。结合案例数据,系统分析了雨洪管理措施在径流量及其污染物控制效果上的差异及成因,可为径流调控与污染治理等实践提供理论参考。     

Fe(Ⅵ)/Na2SO3体系降解阿特拉津效能

利用高铁酸钾活化亚硫酸钠(Fe(Ⅵ)/Na₂SO₃体系),探究其对阿特拉津(ATZ)的降解效能;鉴别了反应体系主要活性组分,并考察了Na₂SO₃投加量、反应溶液pH值和水质背景成分对ATZ降解效能的影响.结果表明:当Fe(VI)和Na₂SO₃的投加量分别为50和200μmol/L时,反应10s后Fe(Ⅵ)/Na₂SO₃体系对ATZ的降解效能达到74.4%,单独Fe(VI)(50μmol/L)和单独Na₂SO₃(200μmol/L)对ATZ的去除率仅为10.2%和7.5%.探针化合物和溶解氧作用等实验证实体系中主要的活性基团为SO₄^·-.在pH=8,Fe(VI)投加量为50μmol/L时,随着Na₂SO₃投加量的增大,Fe(Ⅵ)/Na₂SO₃体系对ATZ的去除效率先增大后减小,其中最佳Na₂SO₃投加量为150~200μmol/L.Fe(Ⅵ)/Na₂SO₃体系在pH 7~10的范围内,均可以快速降解ATZ.在天然水体中,Fe(Ⅵ)/Na₂SO₃体系也可以高效降解ATZ,但是水质背景成分会竞争消耗SO₄^·-,导致Fe(Ⅵ)/Na₂SO₃体系对ATZ的降解效能降低.     

基于氨氮,硝氮及乙酸条件下Anammox菌的培养

为探讨Anammox菌在氨氮、硝氮及乙酸条件下的富集特性,采用某城市污水处理厂A²/O系统中的生物填料作为MBBR的载体直接启动并运行.结果表明,在NH₄⁺-N、NO₃^--N及乙酸为基质的培养条件下,Anammox菌可在部分反硝化和厌氧氨氧化协同作用下快速富集.经过130d的富集培养,MBBR处理负荷（以N计）达到920.79mg/（m²·d）,Anammox活性（以NH₄⁺-N计）达到3 018.19mg/（m²·d）.高通量结果显示,经富集培养后,Ca.Brocadia占比从0.89%增至27.80%,为Anammox菌的主导菌属;Thauera占比从0.01%增至6.75%,Flavobacterium占比从0.29%增至11.72%,为部分反硝化菌的主导菌属.     

医院空调回风口滤网积尘中抗生素抗性基因污染的比较

为了解医院环境中抗生素抗性基因(ARGs)的污染情况与分布特征,于2018年11月至2021年4月期间分批次采集了武汉市两家医院部分病房空调回风口滤网积尘样本127份,对其进行β-内酰胺类ARGs (mecA、bla_TEM、bla_CTX-M、bla_SHV)和碳青霉烯类ARGs (bla_KPC、bla_NDM-1、bla_IMP、bla_VIM、bla_OXA-51)及一类整合酶基因intI 1的定性与定量检测与评价.结果表明,医院不同科室及ICU空调滤网积尘中可检出以上9种β-内酰胺类,碳青霉烯类ARGs及intI 1,平均检出率分别为55.12%、37.64%和81.89%.ICU的β-内酰胺类与碳青霉烯ARGs的平均检出率显著高于外科与内科(P<0.05);4种β-内酰胺类ARGs中的bla_TEM、mecA检出率及其相对丰度在内科、外科最高(P<0.05);ICU的bla_SHV检出率及其相对丰度高于内科、外科(P<0.05).5种碳青霉烯类ARGs中的bla_NDM-1检出率及其相对丰度在内科、外科显著高于bla_KPC、bla_IMP(P<0.05).intI 1与9种ARGs的相对丰度均呈显著正相关(P<0.05).研究结果表明,两家医院不同科室病房空调滤网积尘中存在β-内酰胺类和碳青霉烯类ARGs以及一类整合酶基因intI 1的污染,内科、外科、ICU均以bla_TEM、mecA、bla_NDM-1为主,由此可认为医院不同科室空气及相关环境中可能存在与此等ARGs相关的耐甲氧西林金黄色葡萄球菌、产ESBLs肠杆菌科细菌、耐碳青霉烯大肠埃希菌与鲍曼不动杆菌等耐药菌的现时与既往污染,并且存在ARGs水平转移的风险;ICU空调滤网积尘中β-内酰胺类与碳青霉烯ARGs的污染较内科、外科严重,其中bla_SHV污染高于内科、外科,由此表明,ICU是ARGs及相关耐药菌污染的高风险科室.     

Mechanisms of Pb(II) coprecipitation with natrojarosite and its behavior during acid dissolution

Lead (Pb) coprecipitation with jarosite is common in natural and engineered environments, such as acid mine drainage (AMD) sites and hydrometallurgical industry. Despite the high relevance for environmental impact, few studies have examined the exact interaction of Pb with jarosite and the dissolution behavior of each phase. In the present work, we demonstrate that Pb mainly interacts with jarosite in four modes, namely incorporation, occlusion, physically mixing, and chemically mixing. For comparison, the four modes of Pb-bearing natrojarosite were synthesized and characterized separately. Batch dissolution experiments were undertaken on these synthetic Pb-bearing natrojarosites under pH 2 to simulate the AMD environments. The introduction of Pb decreases the final Fe releasing efficiency of jarosite-type compounds from 18.18% to 3.45%-5.01%, showing a remarkable inhibition of their dissolution. For Pb releasing behavior, PbSO₄ dissolves in preference to Pb-substituted natrojarosite, i.e., (Na, Pb)-jarosite, which primarily results in the sharp increase of Pb releasing concentration (> 40 mg/L). PbSO₄ occlusion by jarosite-type compounds can significantly reduce the release of Pb. The results of this study could provide useful information regarding Fe and Pb cycling in acidic natural and engineered environments.     

A mechanistic study of ciprofloxacin adsorption by goethite in the presence of silver and titanium dioxide nanoparticles

The adsorption behaviors of ciprofloxacin (CIP), a fluoroquinolone antibiotic, onto goethite (Gt) in the presence of silver and titanium dioxide nanoparticles (AgNPs and TiO₂NPs) were investigated. Results showed that CIP adsorption kinetics in Gt with or without NPs both followed the pseudo-second-order kinetic model. The presence of AgNPs or TiO₂NPs inhibited the adsorption of CIP by Gt. The amount of inhibition of CIP sorption due to AgNPs was decreased with an increase of solution pH from 5.0 to 9.0. In contrast, in the presence of TiO₂NPs, CIP adsorption by Gt was almost unchanged at pHs of 5.0∼6.5 but was decreased with an increase of pH from 6.5 to 9.0. The mechanisms of AgNPs and TiO₂NPs in inhibiting CIP adsorption by Gt were different, which was attributed to citrate coating of AgNPs resulting in competition with CIP for adsorption sites on Gt, while TiO₂NPs could compete with Gt for CIP adsorption. Additionally, CIP was adsorbed by Gt or TiO₂NPs through a tridentate complex involving the bidentate inner-sphere coordination of the deprotonated carboxylic group and hydrogen bonding through the adjacent carbonyl group on the quinoline ring. These findings advance our understanding of the environmental behavior and fate of fluoroquinolone antibiotics in the presence of NPs.     

自供电式同步翻转电荷提取电路的优化设计

目的 解决现有接口电路俘能效率低、开关控制电路模块结构复杂等问题。方法 基于电压翻转及电荷提取技术,提出一种自供电式同步翻转电荷提取的压电能量俘获电路(Self-Powered Optimized Synchronous Inversion and Charge Extraction Circuit,SP-OSICE)。该电路设计了2个电压峰值检测电路,检测压电换能器两端电压峰值,并在正峰值处进行一次电压翻转,然后在负峰值处采用同步电荷提取方法,提取压电换能器寄生电容上储存的电荷,提高能量的收集效率。结果 在低负载区,SP-OSICE电路的输出功率略低于SICE电路的输出功率,随着负载电压的增大,SP-OSICE电路的输出功率略高于SICE电路,且可达到全桥整流电路最大输出功率的6倍以上。结论 SP-OSICE电路优化了SICE电路中的开关控制策略,无需整流桥结构,提高了接口电路的输出功率。整体电路采用自供电设计,无需外部辅助电路控制晶体管通断,降低了电路结构的复杂性。仿真和实验结果均验证了SP-OSICE电路的优势。