Comparison of UV and UV-LED activated sodium percarbonate for the degradation of O-desmethylvenlafaxine

As an active metabolite of venlafaxine and emerging antidepressant, O-desmethylvenlafaxine (ODVEN) was widely detected in different water bodies, which caused potential harm to human health and environmental safety. In this study, the comparative work on the ODVEN degradation by UV (254 nm) and UV-LED (275 nm) activated sodium percarbonate (SPC) systems was systematically performed. The higher removal rate of ODVEN can be achieved under UV-LED direct photolysis (14.99%) than UV direct photolysis (4.57%) due to the higher values of photolysis coefficient at the wavelength 275 nm. Significant synergistic effects were observed in the UV/SPC (80.38%) and UV-LED/SPC (53.57%) systems and the former exhibited better performance for the elimination of ODVEN. The degradation of ODVEN all followed the pseudo-first-order kinetics well in these processes, and the pseudo-first-order rate constant (k_obs) increased with increasing SPC concentration. Radicals quenching experiments demonstrated that both ·OH and CO₃·⁻ were involved in the degradation of ODVEN and the second-order rate constant of ODVEN with CO₃·⁻ (1.58 × 10⁸ (mol/L)⁻¹ sec⁻¹) was reported for the first time based on competitive kinetic method. The introduction of HA, Cl⁻, NO₃⁻ and HCO₃⁻ inhibited the ODVEN degradation to varying degrees in the both processes. According to quantum chemical calculation, radical addition at the ortho-position of the phenolic hydroxyl group was confirmed to be the main reaction pathways for the oxidation of ODVEN by ·OH. In addition, the oxidation of ODVEN may involve the demethylation, H-abstraction, OH-addition and C-N bond cleavage. Eventually, the UV-LED/SPC process was considered to be more cost-effective compared to the UV/SPC process, although the UV/SPC process possessed a higher removal rate of ODVEN.     

Nitrogen and phosphorus removal in an airlift intermittent circulation membrane bioreactor

A new airlift intermittent circulation integrated bioreactor was developed for simultaneous nitrogen and phosphorus removal of wastewater, in which, circulation of mixed liquid between mixing zone and aeration zone was realized by aeration power, alternately anaerobic/anoxic bio-environment in mixing zone was realized by intermittent circulation and simultaneous nitrogen and phosphorus removal was obtained through strengthened denitrifying phosphorus removal process. Removal performance of the reactor was investigated and pollutant removal and transfer mechanism in one operation circle was analyzed. The experiment results indicated that under the influent condition of chemical oxygen demand (COD) concentration of 642.1 mg/L, total nitrogen (TN) of 87.4 mg/L and PO₄^3--P of 12.1 mg/L, average removal efficiencies of COD, TN and PO₄^3--P reached 96.4%, 83.2% and 90.5%, respectively, with the hydraulic residence time of 22 hr and operation circle time of 185 min. Track studies indicated that the separation of aeration and mixing zones and intermittent circulation of mixed liquid between the two zones provided distinct biological environments spatially and temporally, which ensured the occurrence of multifunctional microbial reactions.     

A novel co-catalyzed system between persulfate and chlorite by sonolysis for removing triphenylmethane derivative

Triphenylmethane (tpm) derivatives (e.g. tpm_CV) have threatened the safety of the aquatic environment due to the potential toxicity and carcinogenicity. In this study, the novel ultrasonic/persulfate/chlorite (US/S₂O₈²⁻/ClO₂⁻) oxidation process was developed for the effective removal of tpm_CV in wastewater. The apparent non-integer kinetics (n around 1.20) of tpm_CV degradation under different factors (R²_Adj > 0.990) were investigated, respectively. Inhibiting effects of anions were greater than those of cations (except Fe(II/III)). The adding of micromolecule organic acids could regulate degradation towards positive direction. The double response surface methodology (RSM) was designed to optimize tpm_CV removal process, and the acoustic-piezoelectric interaction was simulated to determine the propagation process of acoustic wave in the reactor. The possible degradation pathway was explored to mainly include carbonylation, carboxylation, and demethylation. The estimated effective-mean temperature at the bubble-water interface was calculated from 721 to 566 K after introducing the ClO₂⁻, however, the adsorption or partitioning capacity of tpm_CV in the reactive zone was widened from 0.0218 to 0.0982. The proposed co-catalysis of US/S₂O₈²⁻/ClO₂⁻ was based on the determined active species mainly including ClO₂, SO₄⋅⁻, and ⋅OH. Compared with other US-based processes, the operating cost (3.97 $/m³) of US/S₂O₈²⁻/ClO₂⁻ with the EE/O value (16.8 kWh/m³) was relatively reduced.     

Influence of seasonal temperature change on autotrophic nitrogen removal for mature landfill leachate treatment with high-ammonia by partial nitrification-Anammox process

In this study, a denitrification (DN)–partial nitritation (PN)–anaerobic ammonia oxidation (Anammox) system for the efficient nitrogen removal of mature landfill leachate was built with a zone-partitioning self-reflux biological reactor as the core device, and the effects of changes in seasonal temperature on the nitrogen removal in non-temperature-control environment were explored. The results showed that as the seasonal temperature decreased from 34°C to 11.3°C, the total nitrogen removal rate of the DN-PN-Anammox system gradually decreased from the peak value of 1.42 kg/(m³?day) to 0.49 kg/(m³?day). At low temperatures (<20°C), when the nitrogen load (NLR) of the system is not appropriate, the fluctuation of high NH₄⁺-N concentration in the landfill leachate greatly influenced the stability of the nitrogen removal. At temperatures of 11°C–15°C, the NLR of the system is controlled below 0.5 kg/(m³?day), which can achieve stable nitrogen removal and the nitrogen removal efficiency can reach above 96%. The abundance of Candidatus Brocadia gradually increased with the decrease of temperature. Nitrosomonas, Candidatus Brocadia and Candidatus Kuenenia as the main functional microorganisms in the low temperature.     

Carbonate-induced enhancement of phenols degradation in CuS/peroxymonosulfate system: A clear correlation between this enhancement and electronic effects of phenols substituents

This study investigated the enhancement effects of dissolved carbonates on the peroxymonosulfate-based advanced oxidation process with CuS as a catalyst. It was found that the added CO₃²⁻ increased both the catalytic activity and the stability of the catalyst. Under optimized reaction conditions in the presence of CO₃²⁻, the degradation removal of 4-methylphenol (4-MP) within 2 min reached 100%, and this was maintained in consecutive multi-cycle experiments. The degradation rate constant of 4-MP was 2.159 min⁻¹, being 685% greater than that in the absence of CO₃²⁻ (0.315 min⁻¹). The comparison of dominated active species and 4-MP degradation pathways in both CO₃²⁻-free and CO₃²⁻-containing systems suggested that more CO₃•⁻/¹O₂ was produced in the case of CO₃²⁻deducing an electron transfer medium, which tending to react with electron-rich moieties. Meanwhile, Characterization by X-ray photoelectron spectroscopic and cyclic voltammetry measurement verified CO₃²⁻ enabled the effective reduction of Cu²⁺ to Cu⁺. By investigating the degradation of 11 phenolics with different substituents, the dependence of degradation kinetic rate constant of the phenolics on their chemical structures indicated that there was a good linear relationship between the Hammett constants σ_p of the aromatic phenolics and the logarithm of k in the CO₃²⁻-containing system. This work provides a new strategy for efficient removal of electron-rich moieties under the driving of carbonate being widely present in actual water bodies.     

Seasonal variations, temperature dependence, and sources of size-resolved PM components in Nanjing, east China

Size-segregated ambient particulate matter (PM) samples were collected seasonally in suburban Nanjing of east China from 2016 to 2017 and chemically speciated. In both fine (< 2.1 µm, PM_2.1) and coarse (> 2.1 µm, PM_>2.1) PM, organic carbon (OC) accounted for the highest fractions (26.9% ± 10.9% and 23.1% ± 9.35%) of all measured species, and NO₃⁻ lead in average concentrations of water-soluble inorganic ions (WSIIs). The size distributions of measured components were parameterized using geometric mean diameter (GMD). GMD values of NO₃⁻, Cl⁻, OC, and PM for the whole size range varied from < 2.1 µm in winter to > 2.1 μm in warm seasons, which was due to the fact that the size distributions of semi-volatile components (e.g., NH₄NO₃, NH₄Cl, and OC) had a dependency on the ambient temperature. Unlike OC, elemental carbon (EC), and elements, NH₄⁺, NO₃⁻, and SO₄²⁻ exhibited an increase trend in GMD values with relative humidity, indicating that the hygroscopic growth might also play a role in driving seasonal changes of PM size distributions. Positive matrix factorization was performed using compositional data of fine and coarse particles, respectively. The secondary formation of inorganic salts contributing to the majority (> 70%) of fine PM and 20.2% ± 19.9% of speciated coarse PM. The remaining coarse PM content was attributed to a variety of dust sources. Considering that coarse and fine PM had comparable mass concentrations, more attention should be paid to local dust emissions in future air quality plans.     

Effect of intermittent aeration mode on nitrogen concentration in the water column and sediment pore water of aquaculture ponds

Nitrogen in pond sediments is a major water quality concern and can impact the productivity of aquaculture. Dissolved oxygen is an important factor for improving water quality and boosting fish growth in aquaculture ponds, and plays an important role in the conversion of ammonium-nitrogen (NH₄⁺-N) to nitrite-nitrogen (NO₂^?-N) and eventually nitrate-nitrogen (NO₃^?-N). A central goal of the study was to identify the best aeration method and strategy for improving water quality in aquaculture ponds. We conducted an experiment with six tanks, each with a different aeration mode to simulate the behavior of aquaculture ponds. The results show that a 36 hr aeration interval (T_c = 36 hr: 36 hr) and no aeration resulted in high concentrations of NH₄⁺-N in the water column. Using a 12 hr interval time (T_c = 12 hr: 12 hr) resulted in higher NO₂^?-N and NO₃^?-N concentrations than any other aeration mode. Results from an 8 hr interval time (T_c = 8 hr: 8 hr) and 24 hr interval time (T_c = 24 hr: 24 hr) were comparable with those of continuous aeration, and had the benefit of being in use for only half of the time, consequently reducing energy consumption.     

Humidity and PM2.5 composition determine atmospheric light extinction in the arid region of northwest China

Atmospheric visibility can directly reflect the air quality. In this study, we measured water-soluble ions (WSIs), organic and element carbon (OC and EC) in PM_2.5 from September 2017 to August 2018 in Urumqi, NW China. The results show that SO₄^2?, NO₃^? and NH₄⁺ were the major WSIs, together accounting for 7.32%–84.12% of PM_2.5 mass. Total carbon (TC=OC+EC) accounted for 12.12% of PM_2.5 mass on average. And OC/EC > 2 indicated the formation of secondary organic carbon (SOC). The levels of SO₄^2?, NO₃^? and NH₄⁺ in low visibility days were much higher than those in high visibility days. Relative humidity (RH) played a key role in affecting visibility. The extinction coefficient (b_ext) that estimated via Koschmieder formula with visibility was the highest in winter (1441.05 ± 739.95 Mm^?1), and the lowest in summer (128.58 ± 58.00 Mm^?1). The b_ext that estimated via IMPROVE formula with PM_2.5 chemical component was mainly contributed by (NH₄)₂SO₄ and NH₄NO₃. The b_ext values calculated by both approaches presented a good correlation with each other (R² = 0.87). Multiple linear regression (MLR) method was further employed to reconstruct the empirical regression model of visibility as a function of PM_2.5 chemical components, NO₂ and RH. The results of source apportionment by Positive Matrix Factorization (PMF) model showed that residential coal combustion and vehicle emissions were the major sources of b_ext.     

Electrocoagulation coupled with electrooxidation for the simultaneous treatment of multiple pollutants in contaminated sediments

In situ and simultaneous remediation of a variety of pollutants in sediments remains a challenge. In this study, we report that the combination of electrocoagulation (EC) and electrooxidation (EO) is efficient in the immobilization of phosphorus and heavy metals and in the oxidation of ammonium and toxic organic matter. The integrated mixed metal oxide (MMO)/Fe anode system allowed the facile removal of ammonium and phosphorus in the overlying water (99% of 10 mg/L NH₄⁺-N and 95% of 10 mg/L P disappeared in 15 and 30 min, respectively). Compared with the controls of the single Fe anode and single MMO anode systems, the dual MMO/Fe anode system significantly improved the removal of phenanthrene and promoted the transition of Pb and Cu from the mobile species to the immobile species. The concentrations of Pb and Cu in the toxicity characteristic leaching procedure extracts were reduced by 99% and 97% after an 8 hr operation. Further tests with four real polluted samples indicated that substantial proportions of acid-soluble fraction Pb and Cu were reduced (30%–31% for Pb and 16%–23% for Cu), and the amounts of total organic carbon and NH₄⁺-N decreased by 56%–71% and 32%–63%, respectively. It was proposed that the in situ electrogenerated Fe(II) at the Fe anode and the active oxygen/chlorine species at the MMO anode are conducive to outstanding performance in the co-treatment of multiple pollutants. The results suggest that the EC/EO method is a powerful technology for the in situ remediation of sediments contaminated with different pollutants.     

Combined effects of volume ratio and nitrate recycling ratio on nutrient removal, sludge characteristic and microbial evolution for DPR optimization

The optimization of volume ratio (V_An/V_A/V_O) and nitrate recycling ratio (R) in a two-sludge denitrifying phosphorus removal (DPR) process of Anaerobic Anoxic Oxic-Moving Bed Biofilm Reactor (A²/O-MBBR) was investigated. The results showed that prolonged anaerobic retention time (HRT_An: 1.25→3.75 hr) exerted favorable effect on chemical oxygen demand (COD) removal (57.26%→73.54%), poly-β-hydroxyalkanoates (PHA) synthesis (105.70→138.12 mgCOD/L) and PO₄^3? release (22.3→38.9 mg/L). However, anoxic retention time (HRT_A) and R exhibited positive correlation with PHA utilization (43.87%-81.34%) and denitrifying phosphorus removal (DPR) potential (ΔNO₃^?/ΔPO₄^3?: 0.57-1.34 mg/mg), leading to dramatical TN removal variations from 68.86% to 81.28%. Under the V_An/V_A/V_O ratio of 2:6:0, sludge loss deteriorated nutrient removals but the sludge bioactivity quickly recovered when the oxic zone was recovered. The sludge characteristic and microstructure gradually transformed under the dissolved oxygen (DO) control (1.0-1.5→1.5-2.0 mg/L), in terms of sludge volume index (SVI: 194→57 mL/gVSS), median-particle-size (D₅₀: 99.6→300.5 μm), extracellular polymeric substances (EPS) (105.62→226.18 mg/g VSS) and proteins/polysaccharides (PN/PS) ratio (1.52→3.46). Fluorescence in situ hybridization (FISH) results showed that phosphorus accumulation organisms (PAOs) (mainly Cluster I of Accumulibacter, contribution ratio: 91.79%-94.10%) dominated the superior DPR performance, while glycogen accumulating organisms (GAOs) (mainly Competibacter, contribution ratio: 82.61%-86.89%) was responsible for deteriorative TN and PO₄^3? removals. The optimal HRT_A and R assembled around 5-6.5 hr and 300%-400% based on the PHA utilization and DRP performance, and the oxic zones also contributed to PO₄^3? removal although it showed low dependence on DO concentration and oxic retention time (HRT_O).     

湖滨带氧化还原环境的时空变化及其环境效应

在太湖梅梁湾,沿开阔水体至湖滨带方向,对植被型湖滨带(A区)、裸露型湖滨带(B区)和开阔水体(D区)水体中DO和水/沉积物Eh进行为期1a的现场观测.结果发现,梅梁湾水体DO时空变化明显.B区和D区水体中DO常年饱和,而A区DO浓度较低(年均(5.5±1.7)mg·L-1).在植物生长季,从开阔水体至湖滨植被区溶解氧浓度从12.7 mg·L-1降到4.5 mg·L-1;在非植物生长季则从9.7 mg·L-1降到6.2mg·L-1.湖滨带水体Eh在150 mV左右波动,空间变化趋势与溶解氧变化同步.沉积物Eh也表现出明显的时空变化,在植物生长季,各区沉积物均处于较强的还原状态(-158～-101 mV);而在非植物生长季,由开阔水体向植被型湖滨带Eh逐渐升高.在沉积物的垂直剖面上,开阔水体Eh自表层沉积物向下逐渐降低,而在A区的植被覆盖区则是先降低,大概在5 cm深处开始逐渐升高,于20 cm深左右达到峰值.根据上述植被型湖滨带氧化还原环境的特点,可以推知进行湖滨带生态修复,有利于去除湖泊氮污染.     

一条正在发育的中、新生代裂谷带

沿长乐－南澳断裂带分布有非蛇绿岩型的镁铁、超镁铁质岩块；具中、新生代裂谷型岩浆组合；断裂两侧具有相似的变质岩基底及对应显著的地幔隆升地带。说明该断裂带为一条正在发育的中、新生代裂谷带。     

西藏四江流域自然保护区规划设计研究

针对西藏四江流域自然保护区生态保护与经济的和谐发展,研究了相关影响因子模型,通过调整相关影响因子,就可以在土地利用图的基础上对四江流域自然保护区内核心区、缓冲区、发展区作一个合理的规划。     

应用ADMS确定大气环境防护距离方法探讨

针对目前环评工作中常见的大气环境防护距离和卫生防护距离确定方法的技术难点,提出利用ADMS模式改进确定方法,并比较几种计算方法的优劣,提出结合实际气象条件和地形条件进行确定的可行方案。     

全国干湿分布区动态变化研究

在全球气候变化的背景下,我国的干湿状况发生相应变化。本文主要研究过去60年全国干湿状况动态变化,以便于了解气候变化对我国干湿状况的影响。基于1951~2010年全国756个气象站点的气象数据,根据Penman-Monteith潜在蒸散量方法计算潜在蒸散发量,再结合降水量数据计算干燥度指数。利用干湿区划分阈值,划分1951~2010年不同干湿分区,主要有极端干旱区、干旱区、半干旱区、干性半湿润区、半湿润区、湿性半湿润区、湿润区分区,并研究1951~2010年10年年际动态变化。研究结果表明,全国在总体上趋向于干旱,尤其东北地区最为严重,而北疆地区趋向于湿润。不同年代呈现不同的干湿波动性规律,80年代为湿润时期,90年代为极端干旱时期,半干旱区范围明显增加并往东南移动。本研究对理解我国植被空间分布的变化和生态环境建设具有一定的指导意义。     

水泥工业卫生防护距离确定方法研究

针对目前环评工作中确定水泥工业卫生防护距离的常见方法进行研究。比较行业标准、公式、模式这3种卫生防护距离确定方法,提出确定水泥工业卫生防护距离的最优方案。目的是让卫生防护距离的确定更科学合理,并且减少资源的浪费,在确保人民群众健康的前提下合理利用土地资源。     

建设项目防护距离的确定原则与方法

文章从建设项目防护距离的概念出发,剖析了设置防护距离的实质。对以大气污染为主的建设项目,比较了大气环境防护距离和卫生防护距离的异同,并结合具体案例和文献资料比较了同一项目两种防护距离确定结果,最后提出了此类建设项目防护距离的确定原则和方法。     

2006—2018年中国省级以上开发区的空间分布特征变化

以新的国土空间规划语境为背景,基于核密度估计、标准差椭圆法和分类统计对我国2006—2018年省级以上开发区的密度分布特征变化、发展重心轴向的变化和主体功能区视角下的分布变化做了分析。研究表明：该阶段我国省级以上开发区空间分布的东西差距得到一定缓解,仍存在东部连片集聚、西部据点集中的模式差异。开发区分布的总体重心已经向西北方向移动,发展轴向则由原来的南北轴向转向了东南—西北轴向。从主体功能区视角来看,开发区空间分布格局呈现出外围扩散与局部缩减的动态调整。开发区规模的增长主要集中在重点开发区域,缩减主要发生在生态功能区域。这些新变化将为我国国土空间土地利用优化和国土空间管控实践提供重要参考。     

有机污染物在多孔介质中的残留

土壤、地下水中的有机污染物主要以自由态、挥发态、溶解态和残留态等四种形态存在 ,其中残留态的部分是最难以去除的 ,残留量的多少是关系治理费用及治理时间长短的最关键因素。本文以柴油为代表 ,对地下水饱和区中有机物的残留进行了试验模拟 ,与非饱和区的残余饱和度进行了比较 ,揭示了饱和区中有机污染物残余的特点 ,并深入分析了其机理。结果表明 ,砂性介质中 ,地下水饱和区中有机污染物的残余饱和度显著大于非饱和区中的残余饱和度 ,因此可以有效地利用这一特性 ,通过降低地下水位使饱和区中部分残留态污染物转化为自由态 ,提高去除效率 ;与非饱和区中多孔介质粒径越小 ,残留量越大的特性相反 ,饱和区中测得的残余柴油饱和度随介质粒径的增大而增大。不同水位变动速度的试验结果表明 ,水位变动速度对粘性大于水的柴油的残余饱和度影响可以忽略不计。     

辽宁团山海蚀地貌自然保护区选划研究

根据2003年11月辽宁团山海蚀地貌自然保护区选划研究现场调查,探讨了该区海蚀地貌的成因,评价了海域环境质量和生物多样性,依据海洋自然保护区类型与级别划分原则(GBT17504-1998),确定了保护区类型,并采用定性与定量相结合方法给出了保护区级别。结果表明,保护区海域环境质量总体尚好,生态群落正常,保护区类型符合《海洋自然保护区分类原则》(类别III)相关标准,主要保护对象为海蚀地貌景观,该保护区可建成国家级,这在全国沿海尚不多见。