Co-fermentation of waste activated sludge with food waste for short-chain fatty acids production: effect of pH at ambient temperature

Effect of pH ranging from 4.0 to 11.0 on cofermentation of waste activated sludge (WAS) with food waste for short-chain fatty acids (SCFAs) production at ambient temperature was investigated in this study. Experimental results showed that the addition of food waste significantly improved the performance of WAS fermentation system, which resulted in the increases of SCFAs production and substrate reduction. The SCFAs production at pH 6.0, 7.0, 8.0, and 9.0 and fermentation time of 4 d was respectively 5022.7, 6540.5, 8236.6, and 7911.7 mg COD·L⁻¹, whereas in the blank tests (no pH adjustment, pH 8.0 (blank test 1), no food waste addition, pH 8.0 (blank test 2), and no WAS addition (blank test 3)) it was only 1006.9, 971.1, and 1468.5 mg COD·L⁻¹, respectively. The composition of SCFAs at pH from 6.0 to 9.0 was also different from other conditions and propionic acid was the most prevalent SCFA, which was followed by acetic and n-butyric acids, while acetic acid was the top product under other conditions. At pH 8.0 a higher volatile suspended solids (VSS) reduction of 16.6% for the mixture of WAS and food waste than the sole WAS indicated a synergistic effect existing in fermentation system with WAS and food waste. The influence of pH on the variations of nutrient content was also studied during anaerobic fermentation of the mixture of WAS and food waste at different pH conditions. The release of NH₄⁺-N increased with fermentation time at all pH values investigated except 4.0, 5.0 and in blank test one. The concentrations of soluble phosphorus at acidic pHs and in the blank test one were higher than those obtained at alkaline pHs. Ammonia and phosphorus need to be removed before the SCFAs-enriched fermentation liquid from WAS and food waste was used as the carbon source.     

纳污湿地上覆水中重金属的监测及评价

以武河湿地为研究区域采集上覆水水样,采用ICP-AES法测定湿地水体中重金属的含量,参照有关标准用水质标准级别法对水中重金属污染情况进行了评价。结果表明:武河湿地中重金属Hg污染十分严重,各采样点均有分布且水质属劣Ⅴ类。重金属元素Cd污染并不严重,总体水质较好。重金属元素As、Cr、Cu、Pb在武河湿地中污染较轻近乎无污染,水质为Ⅰ类。由于重金属Hg的污染十分严重所以研究区内综合质量等级在4以上,水质为Ⅴ类和劣Ⅴ类,污染严重。     

阿什河流域地下水脆弱性分区

为识别阿什河流域地下水易污区,基于DRASTIC模型,结合研究区水文地质特点和地下水源地特质,舍弃土壤类型和水力传导系数指标,新增抽水井群影响范围评价指标,得到适用于阿什河流域的DRATIE脆弱性评价体系.借助OpenGeoSys(OGS)软件,模拟研究区抽水与不抽水时的地下水流场,圈划出抽水时流场的变化区域,划分抽水井群影响范围.运用DRATIE模型对研究区进行脆弱性评价,绘制研究区地下水脆弱性分区图,并根据用水趋势进行脆弱性情景分析.结果表明:研究区地下水脆弱性主要为较低、中、较高3个级别;河漫滩和阶地区域较易受到污染,抽水井群影响范围内脆弱性为中等,1号井群每口井抽水量不宜超过3.23×10-2 m3/s,2号井群每口井抽水量不宜超过4.00×10-2 m3/s;其余地区较不易受到污染.研究显示,应严格控制水源地抽水量,以防阿什河水体倒灌;合理分配1、2号井群抽水量,可减小水源地脆弱性范围和等级.      

污染场地地下水中汞污染反应运移模拟

汞（Hg）是人们持续关注的全球环境污染物之一,其对地下水的污染严重威胁着与地下水相关的生态环境系统.汞在地下水系统中的物理与地球化学反应过程的准确刻画是研究汞迁移转化规律的重点和难点.基于某工业场地汞污染数据,首先采用PHREEQC研究地下水中无机二价汞的存在形态,然后利用PHT3D程序建立汞污染物反应性溶质运移二维剖面模型.该模型考虑了汞污染物在地下水系统中的对流、弥散过程及地球化学反应过程（包括水相络合作用、表面络合吸附作用及受动力学控制的氧化还原作用）.结果表明,无机二价汞的存在形态以HgCl₂和Hg（OH）Cl占主导地位,氧化还原作用是影响地下水中汞污染反应性运移的主要控制因素;另一方面,水合氧化铁HFO对汞迁移的阻滞影响较小,而溶解性有机质对汞较强的络合作用不能忽视.本文研究成果可为预测与评估特定污染场地地下水汞污染的变化趋势及制定相应的修复策略提供科学依据.     

The size distribution of airborne bacteria and human pathogenic bacteria in a commercial composting plant

•Bacterial concentrations from eight stages were 10⁴–10⁵copies/m³. •Diameter influenced clustering of bacterial and HPB lineages. •Dg of 8 HPB ranged from 2.42 to 5.09 μm in composting areas. •Dg of 8 HPB ranged from 3.70 to 8.96 μm in packaging areas. •HPB had high concentrations and small sizes in composting areas. Composting plants are regarded as one of the important sources of environmental bioaerosols. However, limitations in the size distribution of airborne bacteria have prevented our comprehensive understanding of their risk to human health and their dispersal behavior. In this study, different sizes of airborne bacteria were collected using an eight-stage impactor from a full-scale composting facility. Size-related abundance and communities of airborne bacteria as well as human pathogenic bacteria (HPB) were investigated using 16S rRNA gene sequencing coupled with droplet digital PCR. Our results indicate that the bacterial concentrations from the eight stages were approximately 10⁴–10⁵copies/m³. Although no statistical correlation was detected between the particle size and the Shannon index, the influence of size on bacterial lineages was observed in both composting and packaging areas. For airborne bacteria from different stages, the dominant phyla were Firmicutes, Proteobacteria, and Actinobacteria, and the dominant genera was Bacillus. Seven out of eight HPB with a small geometric mean aerodynamic diameter had a high concentration in composting areas. Based on diameters of 2.42 to 5.09 μm, most HPB in the composting areas were expected to be deposited on the bronchus and secondary bronchus. However, in the packaging areas, the deposition of HPB (diameters 3.70 to 8.96 μm) occurred in the upper part of the respiratory tract. Our results on the size distribution, abundance, and diversity of these bacteria offer important information for the systematic evaluation of bacterial pathogenicity and the potential health impacts on workers in composting plants and the surrounding residents.     

Discovery of emerging organic pollutants in the atmosphere through an omics approach

● We review the framework of discovering emerging pollutants through an omics approach. ● High-resolution MS can digitalize atmospheric samples to full-component data. ● Chemical features and databases can help to translate untargeted data to compounds. ● Biological effect-directed untargeted analyses consider both existence and toxicity. Ambient air pollution, containing numerous known and hitherto unknown compounds, is a major risk factor for public health. The discovery of harmful components is the prerequisite for pollution control; however, this raises a great challenge on recognizing previously unknown species. Here we systematically review the analytical techniques on air pollution in the framework of an omics approach, with a brief introduction on sample preparation and analysis, and in more detail, compounds prioritization and identification. Through high-resolution mass spectrometry (HRMS, typically coupled with chromatography), the complicated environmental matrix can be digitalized into “full-component” data. A key step to discover emerging compounds is the prioritization of compounds from massive data. Chemical fingerprints, suspect lists and biological effects are the most vital untargeted strategies for comprehensively screening critical and hazardous substances. Afterward, compressed data of compounds can be identified at various confidence levels according to exact mass and the derived molecular formula, MS libraries, and authentic standards. Such an omics approach on full-component data provides a paradigm for discovering emerging air pollutants; nonetheless, new technological advancements of instruments and databases are warranted for further tracking the environmental behaviors, hence to evaluate the health risk of key pollutants.     

厌氧-局部循环供氧生物膜技术处理农村污水

通过模拟农村生活污水水质和间歇进水特点,利用“厌氧-局部循环供氧生物膜”技术,研究该工艺对有机物、氮、磷的去除效果.厌氧池和局部循环供氧池有效容积比为1∶1.6,曝气装置位于局部循环供氧池中间底部,环形导流板将局部循环供氧池分隔成中间好氧区和四周缺氧区,斜管沉淀池前置到厌氧池与局部循环供氧池之间,出水端设置循环水池.装置连续稳定运行12个月,平均进水量为140 L/d,生物反应区HRT为1.3d.监测结果表明,出水COD、BOD、NH3-N、TN和TP平均浓度分别在40.31、3.38、2.69、11.98和0.75 mg/L,达到了国家城镇污水处理厂污染物排放指标(GB-18918-2002)中的一级排放标准.研究表明,厌氧-局部循环供氧技术是一种适合农村分散污水处理的新工艺,可有效减轻农业面源污染.     

活性炭吸附和两级Fenton氧化组合工艺处理高盐对氨基苯酚生产废水

采用活性炭吸附和两级Fenton氧化组合工艺对高盐度对氨基苯酚生产废水进行了处理实验研究。结果表明,p H值对活性炭去除有机物的影响较小。当活性炭投加量为4 g/L时,TOC去除率61%。分级加药可以有效提高Fenton氧化对有机物的去除效率。在温度为25℃、p H为3、30%H2O2投加量为3%(V/V)、Fe2+/H2O2摩尔比为0.05时,两级Fenton氧化处理后,出水TOC降至150 mg/L以下。此外,Fenton氧化后形成氢氧化铁污泥颗粒粒径为4.5μm,经过聚丙烯酰胺(PAM)絮凝之后,污泥的粒径明显增加,过滤特性改善。PAM絮凝效果依赖于溶液的p H值,当p H超过10后会失去作用,故在使用过程中需要严格控制溶液的p H值。     

喀斯特石漠化的研究现状与存在的问题

喀斯特石漠化是土地荒漠化的主要类型之一。喀斯特生态系统的脆弱性决定了喀斯特生态系统的易损性和退化喀斯特生态系统的难恢复性,但它与发生石漠化并没必然的联系,喀斯特石漠化是岩溶生态系统退化的结果,而不是喀斯特生态系统脆弱性的必然表现。故所指的喀斯特石漠化,特指人为加速的石漠化,属于人为荒漠化的一种类型,但强调喀斯特石漠化的人为成因性,并不是否定自然背景对喀斯特生态系统的制约作用。石漠化土地的分类既要能反映出石漠化发生的严重程度,也要能体现石漠化土地的成因和岩性地貌等地质背景对生态学过程的影响,因此,作者提出以“土地利用类型+植被+岩性+地貌+石漠化程度”对人为加速石漠化过程中石漠化土地进行类型划分,以正确评价石漠化土地的生态环境价值。     

南方土壤酸沉降敏感性研究Ⅲ.Si释放与缓冲作用

研究了模拟酸雨淋溶过程中南方主要土壤硅释放量与缓冲机理。结果表明,土壤中存在两个缓冲体系,pH值高于3.0时,土壤以初级缓冲体系为主;pH值低于3.0,尤其是离子淋溶量高于或接近CEC值后,次级缓冲体系成为主要的质子缓冲源。淋溶液pH值的降低可加速矿物风化和Si的释放,从而促进土壤中Si的淋溶,但Si的淋溶同时受到吸附、沉淀与转化过程及土壤初始条件的影响。