活性炭填料塔FeSO4液相催化氧化脱硫

对活性炭及瓷拉西环两种填料用自来水进行脱硫对比实验,证明无论是等宏观表面积还是等填料层高度,活性炭填料的脱硫率均高于瓷拉西环。在活性炭填料塔中进行了FeSO4液相催化氧化脱硫实验,考察了液气比、空塔气速、吸收温度及SO2进口浓度对脱硫率的影响。综合实验结果表明,连续运行500min时,脱硫率及吸收液pH分别稳定在93．5％以上及4．6左右,且两者的变化趋势基本一致。     

Sensitivity of ozone to precursor emissions in urban Beijing with a Monte Carlo scheme

In order to understand the formation mechanisms of high surface ozone and identify the main contributor sources in Beijing, this study investigates the sensitivity of surface ozone to NO, NO₂ and nine types of NMVOC emissions during a photochemical smog episode. Monte Carlo sensitivity analysis scheme with fifty simulations is established based on the Nested Air Quality Prediction Model System (NAQPMS). At every simulation, each of the eleven precursor emissions is perturbed with a distinct set of perturbations. The sensitivities of ozone to emissions are identified by multiple linear regressions. The stability of sensitivity results is validated by two experiments with standard deviations of log-normal perturbations set as 30% and 50% respectively. The sensitivity results suggest that the current high surface ozone is strongly stimulated by NMVOC emissions. Among NMVOC emissions, formaldehyde, ethylene and olefins emissions present the greatest impacts on ozone. On the other hand, NOx emissions have a strong inhibitory effect on ozone formation, even after 50% NOx emission reduction. This indicates that the current ozone formation in Beijing is under NOx-saturated conditions. A transition of ozone formation is observed from NOx-saturated to NOx-limited sensitivity behavior with a 75% reduction of NOx emissions. This study gives the implication that abatement of the four NMVOC types mentioned above could be efficient on reducing the high levels of surface ozone in central urban Beijing, while inadequate abatement in NOx emissions probably induces reverse effects.     

阴极电生H_2O_2及电-Fenton法降解甲基橙

对石墨-PTFE阴极的主要制作参数和在无隔膜系统中电生H2O2的主要工艺参数进行了研究。结果发现,石墨与PTFE的质量比为4∶1~3∶1之间的石墨-PTFE阴极经350℃1 h煅烧后性能最好。采用磁力搅拌代替通常的氧气扩散和空气鼓泡等供氧方法,可简化系统的供氧设备,降低废水的处理成本,更易于放大和实施,且可充分利用阳极电生的氧气。石墨-PTFE阴极有较好的稳定性,重复使用10次之后,电生H2O2的活性没有下降。在由石墨-PTFE阴极和铁阳极组成的电-Fenton系统中对甲基橙溶液进行了降解,脱色效果显著。     

四喷嘴射流曝气器性能的三维数值模拟与实验研究

应用FLUENT对四喷嘴射流曝气器在不同工况下的引射空气性能进行三维数值模拟,分析了射流器内的场分布特性与气液两相流动结构;同时建立射流器性能实验台,对四喷嘴射流曝气器的性能进行实验研究。研究表明,四喷嘴射流器性能较高,能量损失较少,两相流动结构稳定;相对于单喷嘴射流器,四喷嘴射流器的流量比和效率随压力比的变化显著;四喷嘴射流曝气器在工况4下工作性能最好,其流量比q为3.20,效率η为36%,而相似工况下单喷嘴结构流量比q仅为1左右,效率η不超过20%;数值模拟结果与实验结果吻合较好。     

绿色淀粉类絮凝剂的应用研究进展

絮凝沉淀是水处理中的有效方法,天然淀粉经过变性处理可成为优良的絮凝剂,由于其绿色环保、原料来源广和易生物降解等特点,在水处理中得到了广泛应用。本文详细介绍了变性淀粉絮凝剂的种类及应用研究进展,展望了变性淀粉在污水处理领域的发展前景。     

TS-1分子筛催化O3/H2O2氧化乙酸

研究了酸性条件下TS-1分子筛催化O3/H2O2体系(O3/H2O2/TS-1)对降解水中乙酸效率的影响,优化了相关工艺参数,并对其作用机理进行了分析。结果表明,在pH为2.8时,TS-1的加入能显著提高臭氧化的降解效率。优化工艺参数表明,当过氧化氢投加量为3 g/L,TS-1投加量为5 g/L时,O3/H2O2/TS-1体系对乙酸具有较高的降解率,60 min后O3/H2 O2/TS-1体系对乙酸(初始浓度为100 mg/L)的去除率达到了58.7%。当pH为0.8时,O3/H2 O2/TS-1体系对乙酸的去除率仅为19.8%,降解效果较差。定量化计算表明,O3/H2O2和O3/H2O2/TS-1的Rct分别为1.62×10-8和8.67×10-7。通过测定乙酸降解过程水样中过氧化氢和液相臭氧的浓度变化,推测了具体反应机理。由于此体系在酸性条件下对乙酸有较好的降解效果,拓宽了现有O3/H2O2体系的应用范围。     

TS-1分子筛催化O_3/H_2O_2氧化乙酸

研究了酸性条件下TS-1分子筛催化O3/H2O2体系（O3/H2O2/TS-1）对降解水中乙酸效率的影响,优化了相关工艺参数,并对其作用机理进行了分析。结果表明,在pH为2.8时,TS-1的加入能显著提高臭氧化的降解效率。优化工艺参数表明,当过氧化氢投加量为3 g/L,TS-1投加量为5 g/L时,O3/H2O2/TS-1体系对乙酸具有较高的降解率,60 min后O3/H2 O2/TS-1体系对乙酸（初始浓度为100 mg/L）的去除率达到了58.7%。当pH为0.8时,O3/H2 O2/TS-1体系对乙酸的去除率仅为19.8%,降解效果较差。定量化计算表明,O3/H2O2和O3/H2O2/TS-1的Rct分别为1.62×10-8和8.67×10-7。通过测定乙酸降解过程水样中过氧化氢和液相臭氧的浓度变化,推测了具体反应机理。由于此体系在酸性条件下对乙酸有较好的降解效果,拓宽了现有O3/H2O2体系的应用范围。     

基于格网GIS的豫北地区干旱灾害风险区划

以豫北地区32个市县为研究区域,从造成干旱灾害的4个因子,即致灾因子危险性、承灾体暴露性、脆弱性和防灾减灾能力4个角度出发,选取了包括气象、土壤、人口、社会经济在内的17项指标,在格网GIS技术的支持下,对评价体系中的各指标进行10 km×10 km尺度的网格化表达。应用自然灾害风险指数法,熵组合权重法和加权综合分析法,建立了干旱灾害风险评价模型;通过选取典型案例年,运用最优分割理论确定了干旱灾害风险阈值,并利用GIS技术绘制了豫北地区的干旱灾害风险区划图。结果显示:豫北地区的高风险区主要集中在濮阳市区、濮阳县、清丰县、南乐县、新乡市区;而西部的济源市、孟州市,以及原阳县风险较轻。     

基于“3S”技术的村镇住宅洪灾脆弱性曲线研究

脆弱性曲线常用来表示各类承灾体的洪灾损失率与洪水特征之间的关系,是洪灾风险评价方法中的关键部分。为了构建村镇住宅洪灾脆弱性曲线,以2010年永吉县口前镇洪灾为案例,根据抽样理论运用GPS技术开展了村镇住宅洪灾损失的实地调查;运用RS技术和GIS技术提取出洪水淹没水深用以补充未调查房屋的淹没水深数据;采用回归分析方法建立了各类平房住宅水深-损失率之间的关系,用以表征脆弱性曲线。结果表明:居民住宅的洪灾损失率与水深高度相关,且在同一淹没水深下,平房住宅的使用时间越长损失率越大。脆弱性曲线的建立为计算洪灾潜在损失和区域防灾减灾提供了依据。     

Reduction of nitrobenzene in groundwater by iron nanoparticles immobilized in PEG/nylon membrane

The highly reactive iron nanoparticles (NPs) immobilized in nylon membrane were synthesized and characterized, and the reduction of nitrobenzene (NB) in groundwater by the NPs was investigated. Environmental scanning electron microscopy (ESEM) images showed that the NPs distributed homogeneously on the membrane surface without agglomeration. X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) analyses revealed that the NPs immobilized in membrane were mainly composed of Fe-oxides rather than zero-valent iron. Thermogravimetric (TG) analysis suggested that the weight percentage of the immobilized NPs and the oxygen introduced to the reacted sample after 80min reaction were about 18.5% and 13%, respectively. Moreover, Fourier transform infrared (FTIR) analysis further demonstrated the changes on the membrane surface after thermal grafting, NPs immobilizing and reacting for 80min. Using the reactive NPs immobilized in nylon membrane, NB in groundwater was rapidly and quantitatively decreased by 68.9% just in the first 20min, the Fe(2+) associated with the iron NPs immobilized in PEG/nylon66 membrane was mainly responsible for this reduction. The reaction appeared to follow pseudo-first-order kinetics and the rate constants increased upon decreasing the pH value. The samples we prepared exhibited good corrosion resistance for humic acid (HA) but had a short-term performance for NB degradation. More so, the groundwater chemistry had a negative influence on the reactivity of membrane immobilized NPs.