污泥含炭吸附剂对挥发性有机废气吸附实验研究

研究了污泥含炭吸附剂对挥发性有机污染物的吸附特性。结果表明,污泥含炭吸附剂对苯系物的吸附为典型的物理吸附,其吸附甲苯等温线的类型系优惠型吸附等温线,表明具有良好的吸附能力;在吸附反应温度为20℃,气体流量为500 mL/m in(停留时间为0.424 s),甲苯浓度为2 700 mg/m3时,甲苯的饱和吸附容量为150.0 mg/g;同时,研究表明污泥含炭吸附剂对苯系物的饱和吸附容量和吸附强弱次序为二甲苯甲苯苯。结果表明污泥含炭吸附剂适合对中低浓度有机废气的吸附净化。     

ASBBR-二级SBBR-化学除磷组合工艺处理榨菜腌制废水

针对榨菜腌制废水高盐高氮磷高有机物浓度的特征,提出"厌氧序批式生物膜反应器(ASBBR)-二级序批式生物膜反应器(SBBR)-化学除磷"组合处理工艺,在前期对组合工艺中单元工艺的关键工况参数研究的基础上,考察组合工艺的处理效能。实验结果表明,采用该组合工艺,可使进水COD、NH4+-N、TN及PO43--P分别为10 000、345、550和38.5mg/L的榨菜腌制废水,处理出水COD、NH4+-N、TN及PO43--P分别达到93.6、12.3、18和0.1 mg/L,去除率分别为99.1%、96.4%、96.7%和99.9%,出水达到污水综合排放一级标准。     

限氮和限磷对活性污泥合成聚羟基烷酸的影响

聚羟基烷酸(PHA)是微生物在不平衡营养条件下贮存的一种胞内聚合物,限磷和限氮两种方式均有助于活性污泥中的混合菌群合成PHA,研究考察了两种不同方式下活性污泥合成PHA的情况。实验结果表明,当C∶N为125时,活性污泥中PHA的合成量达到细胞干重的59%;当C∶P为750时,活性污泥积累的最大PHA含量占细胞干重的37%,说明限氮和限磷两种方式对活性污泥合成PHA均有很大影响,且限氮方式更有效。     

生物法-人工湿地组合工艺处理小城镇混合污水研究

为适应小城镇污水处理高效、低耗、管理简单的要求,开展了生物法(水解酸化/生物接触氧化)-人工湿地组合工艺(A/BCO-CW)处理小城镇片区混合污水的研究。结果表明,A/BCO系统在停留时间为3～6 h条件下,对悬浮物和有机物有高的去除效率,COD、BOD5和TSS去除率分别达到63.1%、67.7%和66.2%,避免了人工湿地堵塞和提高处理效率,减少了所需湿地面积44%。全年运行结果表明,在0.30～0.59 m/d水力负荷率下,垂直流-表面流-水平潜流人工湿地组合系统对COD、BOD5和TSS平均去除负荷达9.4、5.1和7.2 g/(m2.d)(42%、71.2%和85.2%);COD、BOD5去除速率常数为74.6±12.1 m/y、166±30.5 m/y,这些数值均处于文献中k值范围的高量程内。A/BCO-人工湿地系统对COD、BOD5和TSS具有好的处理效果,出水水质能够稳定达到《地表水环境质量标准》(GB 3838-2002)的IV类水标准,2种处理方法有效组合起来,所开发的低成本、高效率、可持续运行的城镇废水处理组合系统,将会在实际应用尤其是高有机负荷污水处理中发挥良好效用。     

颗粒物对无电压作用下离子交换膜分离去除铜离子的影响

在无外加电压条件下研究了颗粒物对阳离子交换膜分离去除铜离子效果的影响。选用硅酸、二氧化硅、氧化铝和水杨酸等4种物质作为颗粒物分别进行实验,其添加量均为50 mg/L。Cu2+及其补偿离子K+的浓度分别为0.0787mmol/L(5 mg/L)和0.787 mmol/L,水温为25±1℃,搅拌强度为600 r/min,水力停留时间为12 h。在所述实验条件下运行96 h后,水中无颗粒物干扰时,铜离子去除率为84%;水中存在带负电荷颗粒物(硅酸)和不带电荷颗粒物(二氧化硅和氧化铝)时,铜离子去除率略为下降至81%;而当水中存在带正电荷颗粒物(水杨酸)时,铜离子的去除率进一步下降为79%。研究结果表明带正电荷颗粒物对铜离子的交换去除影响较带负电荷或不带电荷颗粒物大,因为带正电荷颗粒物更易迁移至阳离子交换膜表面甚至进入膜内,并与膜表或膜内离子交换基团结合,从而导致铜离子交换去除明显下降。     

壳聚糖改性粘土对高藻水中藻类的絮凝去除

对壳聚糖改性粘土用于天然高藻水中藻类的絮凝去除进行了研究。实验表明,经壳聚糖改性后的粘土对高藻水中藻细胞有较好的去除效果。粘土的种类对除藻效果有一定影响,其中以高粘凹凸棒石为最佳,其最佳投加量为66mg/L(壳聚糖6 mg/L),此时的叶绿素去除率达到95.45%。相比单独投加壳聚糖,粘土的加入增加了絮体密实度,减少了絮体体积,并使絮体分布更均匀。粘土的粒径对絮凝效果基本没有影响,粒径范围在25～74μm时,改性粘土对藻细胞的凝聚效果是一致的。经壳聚糖改性的粘土在酸性条件下絮凝效果较好,当pH值大于7时,其絮凝能力迅速下降。     

厌氧流化床处理白酒废水运行参数的研究

研究了床层膨胀率、HRT、温度以及有机容积负荷冲击等因素对AFB反应器COD去除率的影响。结果显示:温度为32±2℃,进水COD 6 000 mg/L,pH7.2条件下,AFB反应器处理白酒废水的优化运行参数为床层膨胀率为36%,回流比1∶7,水力停留时间8 h,此时废水COD去除率可达80%左右;同时该反应器在有机容积负荷达到36.1 kg COD/(m3.d)时COD去除率明显下降。     

Emission factors and particulate matter size distribution of polycyclic aromatic hydrocarbons from residential coal combustions in rural Northern China

Coal consumption is one important contributor to energy production, and is regarded as one of the most important sources of air pollutants that have considerable impacts on human health and climate change. Emissions of polycyclic aromatic hydrocarbons (PAHs) from coal combustion were studied in a typical stove. Emission factors (EFs) of 16 EPA priority PAHs from tested coals ranged from 6.25 ± 1.16 mg kg^?1 (anthracite) to 253 ± 170 mg kg^?1 (bituminous), with NAP and PHE dominated in gaseous and particulate phases, respectively. Size distributions of particulate phase PAHs from tested coals showed that they were mostly associated with particulate matter (PM) with size either between 0.7 and 2.1 μm or less than 0.4 μm (PM_0.4). In the latter category, not only were more PAHs present in PM_0.4, but also contained higher fractions of high molecular weight PAHs. Generally, there were more than 89% of total particulate phase PAHs associated with PM_2.5. Gas-particle partitioning of freshly emitted PAHs from residential coal combustions were thought to be mainly controlled by absorption rather than adsorption, which is similar to those from other sources. Besides, the influence of fuel properties and combustion conditions was further investigated by using stepwise regression analysis, which indicated that almost 57 ± 10% of total variations in PAH EFs can be accounted for by moisture and volatile matter content of coal in residential combustion.     

活性半焦用于油田含油污水除油的研究

以经济廉价的半焦为原料,制备用于处理油田含油污水的吸附剂。采用高温焙烧活化、水蒸气活化、高压水热活化以及硝酸、氢氧化钾活化等方法对半焦进行活化处理,通过静态吸附实验测定除油率来评价活化效果,重点讨论了氢氧化钾活化条件对除油效果的影响。结果表明:KOH与半焦质量比为6∶1,80℃浸渍3 h,550℃焙烧1.5 h时,制备的活性半焦吸附除油效果最好,除油率可以达到75.6%;活性半焦对油的吸附符合Freund lich吸附方程。利用酸碱滴定法对样品表面酸碱官能团进行分析,发现KOH活化后半焦表面碱性亲油官能团明显增多;通过SEM对半焦的微观结构进行分析,发现KOH活化后半焦产生大量有利于吸附的孔结构。     

Chemical mass balance source apportionment for combined PM2.5 measurements from U.S. non-urban and urban long-term networks

The Minnesota Particulate Matter 2.5 (PM_2.5) Source Apportionment Study was undertaken to explore the utility of PM_2.5 mass, element, ion, and carbon measurements from long-term speciation networks for pollution source attribution. Ambient monitoring data at eight sites across the state were retrieved from the archives of the Interagency Monitoring of Protected Visual Environments (IMPROVE) and the Speciation Trends Network (STN; part of the Chemical Speciation Network [CSN]) and analyzed by an Effective Variance – Chemical Mass Balance (EV-CMB) receptor model with region-specific geological source profiles developed in this study. PM_2.5 was apportioned into contributions of fugitive soil dust, calcium-rich dust, taconite (low grade iron ore) dust, road salt, motor vehicle exhaust, biomass burning, coal-fired utility, and secondary aerosol. Secondary sulfate and nitrate contributed strongly (49–71% of PM_2.5) across all sites and was dominant (≥60%) at IMPROVE sites. Vehicle exhausts accounted for 20–70% of the primary PM_2.5 contribution, largely exceeding the proportion in the primary PM_2.5 emission inventory. The diesel exhaust contribution was separable from the gasoline engine exhaust contribution at the STN sites. Higher detection limits for several marker elements in the STN resulted in non-detectable coal-fired boiler contributions which were detected in the IMPROVE data. Despite the different measured variables, analytical methods, and detection limits, EV-CMB results from a nearby IMPROVE-STN non-urban/urban sites showed similar contributions from regional sources – including fugitive dust and secondary aerosol. Seasonal variations of source contributions were examined and extreme PM_2.5 episodes were explained by both local and regional pollution events.