基于洪水演进数值模拟的溃坝危害性快速评估

采用部分溃坝模型与堰流相交算法计算溃坝最大流量,并基于四次抛物线概化方法得到溃坝洪水的流量过程线;利用洪峰展平法将洪水波概化为三角形,对洪水演进过程进行模拟,分析溃口宽度和溃口形态对洪水演进过程的影响;研究考虑不同溃坝条件下对溃坝洪水的到时、最大流量、水深和洪水历时等洪水演进的主要参数的快速估算方法,以实现对地震可能引发不同溃坝事件危害性的快速评估。     

煅烧的水滑石同时去除水体中砷和氟

为探讨水滑石类材料对水体中氟、砷离子的同时去除效果,采用共沉淀法合成(Mg∶Al=2∶1)纳米类水滑石(LDHs),用傅立叶转换红外光谱、电子扫描透射电镜、X射线晶体衍射等手段对合成的材料进行了表征,并研究纳米材料在不同初始浓度、pH、吸附时间、阴离子干扰条件下其同时除砷氟性能。结果表明,煅烧后的水滑石(LDOs)对砷最大吸附量为51.02 mg/g,对氟最大吸附量为36.63 mg/g。吸附动力学实验表明,煅烧水滑石对砷的吸附在前6 h内基本完成,对氟的吸附在前10 h内基本完成。砷氟共存溶液保持pH=4~10及pH=6~8时,水滑石分别对砷、氟保持良好的吸附效率。对比不同阴离子对水滑石共除砷氟效率的影响,水滑石除砷速率受到阴离子影响力大小为:HPO2-4CO2-3NO-3Cl-SO2-4;水滑石除氟速率受到阴离子影响力大小为:CO2-3HPO2-4SO2-4Cl-NO-3。材料再生循环利用4次后,对砷和氟的吸附效率均能达到90%以上。实验结果表明,所合成的水滑石是一种优秀的能共除砷氟的吸附剂。     

Reprint of: Concentrations, distribution, and bioaccumulation of synthetic musks in the Haihe River of China

Seven typical synthetic musks (SMs) in the samples from the surface water, sediment and fish of the Haihe River were measured. The SM concentrations in the sediment and surface water of the Haihe River were significantly lower than those in the Dagu Drainage River and Chentaizi Drainage River (p < 0.05). Along the flow direction, the SM concentrations in surface water and sediment tended to increase from the upstream to the downstream of Dagu Drainage River. The Bioaccumulation factors (BAFs) of galaxolide (HHCB) and tonalide (AHTN) were calculated at high levels in the muscles of crucian carp, common carp, and silver carp. Most of the biota-sediment accumulation factors (BSAFs) for HHCB and AHTN were higher than 1.7, suggesting magnification possibly exist in the musk bioaccumulations of the three fishes in the Haihe River. No significant differences in HHCB/AHTN ratios were observed among the water, fish, and sediment samples (p > 0.05). However, the HHCB/AHTN values in the Haihe River were much lower than those in the Dagu Drainage River and Chentaizi Drainage River (p < 0.05). Compared with several typical persistent organic pollutants (POPs), the musk concentrations were higher or comparable in the Haihe River.     

武汉地区水环境中全氟化合物污染水平及其分布特征

武汉作为中国氟化工行业的主要生产基地之一,其水环境中全氟及多氟类化合物(PFASs)污染情况对评估该地区水环境生态安全至关重要。采集了武汉城区10个污水处理厂进、出口污水和19个地表水样品,利用HPLC-ESI-MS/MS技术分析研究该区域水环境中PFASs污染水平及其分布特征。结果发现,武汉地区的污水和地表水样品中,PFASs污染均以短链同系物全氟丁酸(PFBA)和全氟丁基磺酸(PFBS)为主。污水处理厂进、出口污水中PFASs总浓度分别为11.8~12 700 ng·L~(-1)和19.1~9 970 ng·L~(-1)。在城区15个湖水样品中,PFASs总浓度为21.0~10 900 ng·L~(-1);在流经城区的4个江水样品中,PFASs总浓度为4.11~4.77 ng·L~(-1),比湖水样品中PFASs浓度水平低1~2个数量级。与污水中PFASs空间分布趋势一致,各湖泊水样中PFASs总体水平呈现汉口汉阳武昌的趋势,表明城市工业布局与人口密度程度直接影响城市PFASs污染空间分布。值得注意的是,与以往水环境中PFASs污染以全氟辛酸(PFOA)和全氟辛基磺酸(PFOS)为主不同,武汉地区水环境中PFASs污染以短链同系物为主,表明短链替代效应已经渐渐在中国化工领域出现,中国全氟行业在响应国际组织规范和建议的基础上做出了实质性进展。然而,对于短链PFASs的污染特征、迁移运输以及生态风险等科学问题,还需要更进一步的研究。     

Development of quantitative structure-property relationship model for predicting the field sampling rate ( R s ) of Chemcatcher passive sampler

Passive sampling technology has been considered as a promising tool to measure the concentration of environmental contaminants. With this technology, sampling rate (Rs) is an important parameter. However, as experimental methods employed to obtain the Rs value of a given compound were time-consuming, laborious, and expensive. A cost-effective method for deriving Rs is urgent. In addition, considering the great dependence of Rs value on water matrix properties, the laboratory measured Rs may not be a good alternative for field Rs. Thus, obtaining the field Rs is very necessary. In this study, a multiparameter quantitative structure-property relationship (QSPR) model was constructed for predicting the field Rs of 91 polar to semi-polar organic compounds. The determination coefficient (R2Train), leave-one-out cross-validated coefficient (Q2LOO), bootstrap coefficient (Q2BOOT), and root mean square error (RMSETrain) of the training set were 0.772, 0.706, 0.769, and 0.230, respectively, while the external validation coefficient (Q2EXT) and RMSEEXT of the validation set were 0.641 and 0.253, respectively. According to the acceptable criteria (Q2 > 0.600, R2 > 0.700), the model had good robustness, goodness-of-fit, and predictive performances. Therefore, we could use the model to fill the data gap for substances within the applicability domain on their missing Rs value.     

Role of interfacial electron transfer reactions on sulfamethoxazole degradation by reduced nontronite activating H2O2

It has been documented that organic contaminants can be degraded by hydroxyl radicals ( • OH) produced by the activation of H₂ O₂ by Fe(II)-bearing clay. However, the interfacial electron transfer reactions between structural Fe(II) and H 2 O 2 for • OH generation and its effects on contaminant remediation are unclear. In this study, we first investigated the relation between • OH generation sites and sulfamethoxazole (SMX) degradation by activating H₂O₂ using nontronite with different reduction extents. SMX (5.2–16.9 μmol/L) degradation first increased and then decreased with an increase in the reduction extent of nontronite from 22% to 62%, while the • OH production increased continually. Passivization treatment of edge sites and structural variation results revealed that interfacial electron transfer reactions between Fe(II) and H 2 O 2 occur at both the edge and basal plane. The enhancement on basal plane interfacial electron transfer reactions in a high reduction extent rNAu-2 leads to the enhancement on utilization efficiencies of structural Fe(II) and H 2 O 2 for • OH generation.However, the • OH produced at the basal planes is less efficient in oxidizing SMX than that of at edge sites. Oxidation of SMX could be sustainable in the H 2 O 2 /rNAu-2 system through chemically reduction. The results of this study show the importance role of • OH generation sites on antibiotic degradation and provide guidance and potential strategies for antibiotic degradation by Fe(II)-bearing clay minerals in H 2 O 2 -based treatments.     

新冠肺炎疫情对农村人居环境整治的影响

新型冠状病毒肺炎（COVID-19,简称“新冠肺炎”）疫情的发生,影响了我国经济水平较低、环境管控力度较薄弱的农村地区的发展.通过对新冠肺炎防疫过程与农村人居环境整治工作间的相互关系进行剖析,探究新冠肺炎疫情防控对农村人居环境整治的主要影响.结果表明,农村垃圾堆积、污水处理不当、厕所粪污无害化处理不达标以及基础设施建设不完善等农村人居环境薄弱环节,存在形成病毒传播扩散途径的风险.而交通运输限制虽然有效抑制了新冠肺炎疫情扩散,但也致使农村人居整治工作延滞.同时,新冠肺炎疫情的传播扩散在短期内限制了农民行为活动,降低了群众对农村人居环境整治工作的热情.据此,建议应健全农村人居环境整治制度,完善整治工程技术,从而在有效管控新冠肺炎疫情传播的同时,更好地推进农村人居环境整治,提高农民生活质量,为疫情过后恢复农民生活、农业生产以及农村发展打下坚实的基础.      

聚苯胺/蒽醌修饰碳毡作为阴极在电芬顿中的应用

通过电化学的方法制备了经2-蒽醌磺酸钠（AQS）和聚苯胺（PANI）修饰的碳毡（CF）电极,探究其作为阴极应用于电芬顿系统中降解有机污染物的特征和影响因素及电化学稳定性.实验结果表明：经AQS/PANI修饰后碳毡阴极的电子转移内阻显著降低,仅为未修饰碳毡电极的0.21%,电化学活性显著提高.相同实验条件下修饰后的电极产过氧化氢的量约是未修饰电极的10倍.在阴极电位为-0.5 V,pH值为2以及Fe²⁺浓度为0.1 mmol·L^-1的条件下,60 min内罗丹明B的降解率可达96.46%.而在同样的实验条件下,CF、AQS/CF和PANI/CF分别作为阴极时,电芬顿体系对于罗丹明B的降解率分别为24.57%、64.29%和72.97%,均低于AQS/PANI/CF阴极.在此基础上,进一步开展自由基的淬灭实验和EPR实验,结果表明经AQS/PANI修饰后的碳毡阴极可有效催化还原分子氧产生超氧自由基,超氧自由基进一步转化为芬顿反应过程中所需的过氧化氢.     

不同补贴机制下的农村清洁取暖价格政策分析

补贴是北方农村清洁取暖价格政策的重要方面,确保兼顾清洁能源替代和农村居民取暖福利,从而实现政策的可持续性. 基于天津、衡水、德州3个城市的实地调研数据,通过配对样本t检验、多元回归和费用效益分析方法,探究了不同补贴机制下的清洁取暖价格政策对居民用能行为和取暖福利的影响. 结果表明:①清洁取暖价格政策会导致取暖成本增加,补贴会显著提高用气量和体感温度,但使各城市面临较大财政压力. ②各地农村清洁取暖价格政策在对用能行为、污染减排效果的影响方面存在较大差异. ③一次性补贴通过减少清洁能源消费量同时增加体感温度,提供了扭曲的价格信号. ④家庭收入显著影响清洁取暖价格政策效果. 因此,一次性补贴需要向从量补贴转变,补贴可以考虑向低收入家庭倾斜或者实施阶梯化的补贴. 为建立清洁取暖长效机制,一方面可以考虑针对农村清洁取暖建立区域大气污染补偿机制,从而推动各地建立因地制宜的清洁取暖价格补贴机制;另一方面可通过改进清洁取暖技术来降低成本,同时开发多种形式的清洁能源. 从长远看,仍需要增加农民保持可接受的收入水平的机会,逐步降低农村居民对清洁取暖补贴的依赖性.