重稀土元素钇对短程反硝化工艺的影响

研究重稀土元素钇（Y（III））对短程反硝化工艺的短期和长期影响.结果表明,1~50mg/L的Y（III）对亚硝酸盐的积累量无明显影响,60~100mg/L的Y（III）会影响硝酸盐的还原和亚硝酸盐的积累.1~10mg/L的Y（III）对细菌活性呈现促进作用,20~100mg/L的Y（III）对细菌活性呈现抑制作用.胞外吸附的Y（III）是抑制细菌活性的主要因子,线性拟合的相关性系数R²为0.957,半抑制浓度IC_50（吸附）为1.079mg/L（以湿重计）,对应水中Y（III）浓度为54.35mg/L.SEM显示,添加Y（III）会使细菌产生更多的胞外聚合物（EPS）将细菌包裹以抵抗Y（III）的毒性,EDS显示被包裹的细菌表面碳、氮元素含量大幅度降低,EPS影响了底物的传质.130d的长期实验表明,5mg/L的Y（III）会使反应器的反硝化性能逐渐消失,停止添加稀土后,反应器的亚硝酸盐积累功能也不能恢复.     

Comparing dark- and photo-Fenton-like degradation of emerging pollutant over photo-switchable Bi2WO6/CuFe2O4: Investigation on dominant reactive oxidation species

The extensive use of tetracycline hydrochloride (TCH) poses a threat to human health and the aquatic environment. Here, magnetic p-n Bi₂WO₆/CuFe₂O₄ catalyst was fabricated to efficiently remove TCH. The obtained Bi₂WO₆/CuFe₂O₄ exhibited 92.1% TCH degradation efficiency and 50.7% and 35.1% mineralization performance for TCH and raw secondary effluent from a wastewater treatment plant in a photo-Fenton-like system, respectively. The remarkable performance was attributed to the fact that photogenerated electrons accelerated the Fe(III)/Fe(II) and Cu(II)/Cu(I) conversion for the Fenton-like reaction between Fe(II)/Cu(I) and H₂O₂, thereby generating abundant ?OH for pollutant oxidation. Various environmental factors including H₂O₂ concentration, initial pH, catalyst dosage, TCH concentration and inorganic ions were explored. The reactive oxidation species (ROS) quenching results and electron spin resonance (ESR) spectra confirmed that ?O₂^? and ?OH were responsible for the dark and photo-Fenton-like systems, respectively. The degradation mechanisms and pathways of TCH were proposed, and the toxicity of products was evaluated. This work contributes a highly efficient and environmentally friendly catalyst and provides a clear mechanistic explanation for the removal of antibiotic pollutants in environmental remediation.     

Aging of PVDF and PES ultrafiltration membranes by sodium hypochlorite: Effect of solution pH

Sodium hypochlorite (NaClO) is a commonly applied cleaning agent for ultrafiltration membranes in water and wastewater treatment. Long-term exposure to NaClO might change the properties and performance of polymeric membranes, and ultimately shorten membrane lifespan. Active species in NaClO solution vary with solution pH, and the aging effects can change depending on the membrane material. In this study, the aging of polyvinylidene fluoride (PVDF) and polyethersulfone (PES) membranes by NaClO at pH 3–11 was investigated by examining variations in chemical composition, surface charge, surface morphology, mechanical strength, permeability, and retention ability. Polyvinyl pyrrolidone (PVP), which was blended in both membranes, was oxidized and dislodged due to NaClO aging at all investigated pH values, but the oxidation products and dislodgement ratio of PVP varied with solution pH. For the PVDF membrane, NaClO aging at pH 3–11 caused a moderate increase in permeability and decreased retention due to the oxidation and release of PVP. The tensile strength decreased only at pH 11 because of the defluorination of PVDF molecules. For the PES membrane, NaClO aging at all investigated pH resulted in chain scission of PES molecules, which was favored at pH 7 and 9, potentially due to the formation of free radicals. Therefore, a decrease in tensile strength and retention ability, as well as an increase in permeability, occurred in the PES membrane for NaClO aging at pH 3–11. Overall, the results can provide a basis for selecting chemical cleaning conditions for PVDF and PES membranes.     

Identification of close relationship between atmospheric oxidation and ozone formation regimes in a photochemically active region

Understanding ozone (O₃) formation regime is a prerequisite in formulating an effective O₃ pollution control strategy. Photochemical indicator is a simple and direct method in identifying O₃ formation regimes. Most used indicators are derived from observations, whereas the role of atmospheric oxidation is not in consideration, which is the core driver of O₃ formation. Thus, it may impact accuracy in signaling O₃ formation regimes. In this study, an advanced three-dimensional numerical modeling system was used to investigate the relationship between atmospheric oxidation and O₃ formation regimes during a long-lasting O₃ exceedance event in September 2017 over the Pearl River Delta (PRD) of China. We discovered a clear relationship between atmospheric oxidative capacity and O₃ formation regime. Over eastern PRD, O₃ formation was mainly in a NO_x-limited regime when HO₂/OH ratio was higher than 11, while in a VOC-limited regime when the ratio was lower than 9.5. Over central and western PRD, an HO₂/OH ratio higher than 5 and lower than 2 was indicative of NO_x-limited and VOC-limited regime, respectively. Physical contribution, including horizontal transport and vertical transport, may pose uncertainties on the indication of O₃ formation regime by HO₂/OH ratio. In comparison with other commonly used photochemical indicators, HO₂/OH ratio had the best performance in differentiating O₃ formation regimes. This study highlighted the necessities in using an atmospheric oxidative capacity-based indicator to infer O₃ formation regime, and underscored the importance of characterizing behaviors of radicals to gain insight in atmospheric processes leading to O₃ pollution over a photochemically active region.     

典型海域船舶用铜材表面生物污损与腐蚀性能研究

目的 对比研究铜合金、紫铜在我国黄海、东海和南海海域具有代表性的港口海水环境中的污损、腐蚀行为.方法 依据GB 12763.6—2007《海洋调查规范》和GB/T 5776—2005《金属和合金的腐蚀试验方法》,通过实海挂片研究ZQMnD12-8-3-2、铜镍合金B10/B30和紫铜T2在我国典型海域青岛港口、舟山港口、三亚港口的生物污损与腐蚀状况.结果 铜镍合金B10、B30和紫铜T2在三海域均具有良好的抑制污损生物附着的性能,其中紫铜抑制污损生物附着的性能最为突出,但其腐蚀严重,腐蚀速率为3.97×10–2～8.48×10–2 mm/a;铸造青铜ZQMnD12-8-3-2虽然含铜量略高于铜镍合金B30,但由于其腐蚀产物易附着于材料表面,其污损抑制性能较差.结论 铜镍合金B10、B30和紫铜T2均有抑制污损生物附着的性能,但受不同海域环境因素和材料表面腐蚀产物致密性的影响有所差异.受泥沙水质影响,舟山港口内铜合金的腐蚀速率较高,腐蚀显著,三亚港口内紫铜的腐蚀速率最高.     

绿色技术专利强制许可法律问题研究

绿色技术专利强制许可要求将环境利益明确纳入公共利益范围,而专门的绿色技术专利强制许可制度则进一步要求针对绿色技术构建特殊许可通道。功能主义观念以环境保护目标的必要性来证成绿色技术专利强制许可的正当性,但没有解释绿色技术、环境保护、公共利益之间的具体联系,从而不能证明绿色技术专利强制许可背后的法律逻辑。法治主义视角下,从强制许可事由、审查程序以及许可费三方面来看,该制度会引起一系列的正当性问题。未来需要将专门的绿色技术专利强制许可制度限定在政府实施的范围内,并依据权利人自认来确定绿色技术的范围。     

城市不同类型高架快速路噪声影响

参照《城市快速路设计规程》(CJJ 129—2009)并用Cadna/A软件对3种类型的城市高架快速路进行声场模拟;对高架类型、道路限速、预测点噪声值三者进行方差分析并评判高架类型对预测点噪声值的影响程度。结果表明,高架声影区只对高度低于高架且与高架距离较近的预测点影响较大,地面道路对1~2层预测点的噪声值影响较大;双层分离式在1~8层表现出更强的噪声污染性,噪声最大值出现在第6层附近,单层分离式及整体式产生的噪声最大值所在楼层数随建筑物与高架之间距离的增大而升高,单层分离式对各楼层的噪声污染程度都较小。高架类型、道路限速对噪声值的影响显著,道路交通量的大小可以改变高架类型及道路限速对于预测点噪声的效应量大小。     

初始扰动对CO2抑制瓦斯爆炸特性研究*

为了预防实际生产过程中发生的瓦斯爆炸事故,利用20 L球形爆炸装置,通过改变粉尘仓充压压力产生不同的扰动,研究9.5%CH4浓度下不同扰动条件对CO2抑爆特性的影响。通过对所得参数进行分析,得到CO2抑爆特性与初始扰动的关系。研究结果表明:相较于均匀静置状态,初始扰动的存在均能提高CH4的爆炸强度,当引发初始扰动的粉尘仓压力为1.5 MPa时,最大爆炸压力达到0.78 MPa;随CO2浓度增大,爆炸强度整体下降,呈二次下降趋势、最大爆炸压力时间呈上升趋势,且各初始扰动压力间爆炸强度均大于均匀静置状态、最大爆炸压力时间小于均匀静置状态;同时利用CHEMKIN软件得到绝热平衡压力,计算热损失参数发现,同一气体混合比例工况下,初始扰动状态的热损失及热损失分数明显低于均匀静置状态的,且当CO2浓度为15%时,差距最大,不同初始扰动间热损失及热损失分数最小值分别为0.013 19 kJ/m2,17.9%,远小于静置状态下0.036 29 kJ/m2,46.4%,说明初始扰动对于CO2抑爆效果存在削弱作用。     

基于时序片段的油气管道运行工况识别方法*

为准确识别管道系统运行工况,提高对油气管道突发事故的响应速度,综合提升管网安全管理水平,提出1种基于时序片段的油气管道运行工况识别方法。首先,构建基于概率分布的状态变化识别模型,提取油气管道中不同运行状态点;其次,建立基于时间序列片段的工况识别模型,快速识别不同时间长度内油气管道运行工况;最后,以国内某成品油管道为例进行方法验证。研究结果表明:该方法可有效识别成品油管道阀门开关状态、泵异常停机和阀门内漏3种运行工况。对比传统的识别方法,该方法可降低状态变化点的漏报率,提升管道运行工况识别的准确率。研究结果可为油气管道系统运行工况识别提供新的借鉴方法。     

稻田落干过程砷甲基化效率变化与关键影响因素分析

研究稻田落干过程砷甲基化效率变化规律,分析关键环境和生物因素的影响,为今后水稻直穗病防控提供科学依据.开展室内培养模拟稻田落干过程,以采集自贵州兴仁（XR）和广西南丹（ND）的两种砷污染水稻土壤为供试土壤,各土壤设置添加（RS）和不添加（CK）水稻秸秆处理,分析自然落干0、24、36、48和60 h过程中Eh、pH、孔隙水总有机碳（TOC）、砷形态、砷甲基化功能基因（arsM）、硫酸盐还原菌（dsrA,砷甲基化相关微生物）、产甲烷菌（mcrA,砷去甲基化相关微生物）丰度和arsM功能微生物多样性变化.稻田落干过程土壤Eh由完全淹水状态下的-300~-200 mV向落干后的-150~-50 mV变迁,而pH值变化规律不明显;孔隙水无机砷（iAs）和二甲基砷（DMAs）浓度随落干过程变化更为显著,总体呈现增加趋势,且RS处理DMAs浓度显著高于CK,ND土壤孔隙水比XR土壤孔隙水DMAs浓度更高;随落干时间延长,XR-CK和XR-RS处理土壤砷甲基化效率有一定提升,但变化不显著,而ND-CK和ND-RS处理土壤砷甲基化效率显著增加.当培养为60 h时,ND-CK和ND-RS处理砷甲基化效率相比培养初期分别提高约61.8%和23.2%;随落干时间延长arsM和dsrA基因拷贝数明显增加,而mcrA基因拷贝数显著下降.秸秆添加后显著提高全细菌和arsM、dsrA和mcrA基因丰度;进一步基于多因素方差分析和冗余分析发现,供试土壤、秸秆添加、落干时间和其交互作用对于各砷形态、砷甲基化效率和关键基因丰度变化影响显著,TOC、Eh和砷甲基化相关基因与甲基态砷呈正向关联,而与无机砷iAs呈负向关联;基于arsM微生物测序发现,伴随落干过程还发生着砷甲基化功能微生物群落的更替.研究结果有助于提升稻田落干过程中砷甲基化变化的理论认知,为今后水稻直穗病科学防控提供指导.