自燃煤矸石山覆盖材料压缩及压实特性实验

自燃煤矸石山表面构建覆盖层,需要具备一定的低渗透性能以有效阻隔空气,防止煤矸石山内部发生自燃。本研究通过室内实验,测定煤矸石山构建覆盖层涉及的碾压材料包括黄土、粉煤灰及掺有粉煤灰的混合土样的界限含水率、一维压缩特性及压实特性,揭示和分析7种覆盖材料配方的压缩压实特性,表明覆盖材料通过碾压可有效阻隔空气,起到阻燃作用;将粉煤灰掺人到一般黄土材料中,可减缓混合土样击实曲线的陡峭性,从而降低材料在碾压中对含水率的敏感度。实验旨在为进行煤矸石山覆盖层碾压提供科学的实验数据及设计参数。     

纳污水体中好氧脱氮菌的筛选与氨氮去除特性

采用异养硝化培养基从城市纳污水体中富集好氧脱氮菌,将得到的富集菌种分离纯化,得到1株好氧脱氮菌NC1,对氨氮的去除率为72.6%;好氧菌株NC1繁殖较快,生长3~4 h即进入对数生长期,有一定实用意义。考察了在不同条件下菌NC1对氨氮的去除效果,发现当pH为6~9之间、转速超过100 r/min、温度为30℃、碳氮比为6~12时对氨氮的去除效果较好。NC1在去除氨氮过程中pH值升高,且能在异养条件下利用亚硝酸盐和硝酸盐生长。     

厌氧后猪场废水资源化制备微生物絮凝剂

通过检测碳源、氮源、磷酸盐和pH等对微生物絮凝剂絮凝率的影响,考察了红平红球菌利用厌氧处理后的猪场废水生产微生物絮凝剂的性能。通过正交实验研究各因素对絮凝率的交互影响以及影响程度的相对大小,从而确定了最佳培养基。结果表明,1.0 L厌氧处理后的猪场废水中加入蔗糖10.0 g、KH2PO42.0 g、K2HPO45.0 g、NaCl 1.0 g、Mg-SO40.2 g,在温度30℃、摇床速度120 r/min、pH=8的条件下发酵72 h后,发酵液的絮凝率可达到92.57%。表明厌氧处理后的猪场废水中加入适量的蔗糖和磷酸盐,完全可以作为一种有效的生产微生物絮凝剂的培养基。     

天然锰砂去除水中的砷

天然锰砂是一种廉价、高效的水处理用材料,但尚未用于水中砷的去除。实验研究了反应时间、砷形态、初始砷浓度、温度、溶液初始pH对吸附过程的影响。结果表明,天然锰砂对As(Ⅲ)的吸附能力大于As(Ⅴ)。25℃时,固液比为10 g/L的条件下,天然锰砂对初始浓度为5.0 mg/L的砷溶液吸附过程经72 h基本达到平衡,平衡时对As(Ⅲ)和As(Ⅴ)的去除率分别达到94.5%和85.9%。吸附过程符合Lagergren准一级反应动力学模型和假二级反应动力学模型。相比之下,假二级动力学模型拟合程度更高。对As(Ⅲ)和As(Ⅴ),45℃时的吸附量均大于25℃时。不同温度下,天然锰砂对As(Ⅲ)和As(Ⅴ)的吸附过程更符合Freundlich等温吸附模型。在溶液初始pH为3～10范围内,锰砂对砷的吸附能力受pH的影响较小。实验结果表明,天然锰砂是一种具有实际应用潜力的除砷材料。     

低温喹啉降解菌的筛选及降解性能

从吉林石化污水处理厂的活性污泥中驯化、筛选获得一株降解效率高且生长速率快高效耐冷菌,命名为WS-5。该菌能以喹啉作为惟一的碳源、氮源及能源。结合菌体的形态观察、生理生化特性实验及16S rDNA 序列同源性对比分析,鉴定菌株WS-5为恶臭假单胞菌(Pseudomonas putida)。不同降解条件下的实验结果表明,菌株WS-5的最佳降解条件是投菌量为15%,pH值范围在8~10,摇床转速为100 r/min。最佳降解环境下对200 mg/L的喹啉在132 h降解率达到了85.3%。菌株WS-5对初始喹啉浓度为50、100、200和300 mg/L的初始喹啉浓度分别在36、72、192和262 h内完全降解。这将为今后在低温条件下处理含喹啉废水提供技术指导。     

铅锌矿尾矿制备陶粒处理选矿废水

以铅锌矿浮选尾矿为原料,水玻璃和木质素作为添加剂,通过高温焙烧,制备水处理陶粒,并用其对选矿废水进行了吸附处理实验研究。实验结果表明,在不添加任何添加剂的条件下,800℃左右烧制的陶粒对选矿废水的COD吸附效果较好,COD去除率达到87.1%;当木质素+水玻璃作为粘结剂烧制陶粒时,不仅陶粒散落减少,COD的去除率和吸附容量都有所增加,COD去除率达到了88.21%,从而达到了"以废治废"的目的。     

超声波-膜生物法联合处理垃圾焚烧厂渗滤液

采用超声波-膜生物法(MBR)联合处理垃圾渗滤液,探讨了超声波辐射时间和MBR的水力负荷对COD、NH3-N和TP去除的影响。结果表明,(1)超声波单独处理时,超声波辐射时间在30～90 s时,COD、NH3-N最大增加率分别34.31%、3.36%,而对TP的去除没有影响;(2)超声波-膜生物(MBR)联合处理时,超声波辐射时间为300 s,MBR的水力负荷为6.4 L/(m2.d)时,COD、NH3-N和TP的最佳去除率分别为92.20%、80.10%和91.12%;MBR的水力负荷为12.8 L/(m2.d),超声波辐射时间在5～20 min时,COD、NH3-N的最佳去除率分别为92.34%、79.93%,TP的浓度低于0.2 mg/L;MBR反应时间为7 h,超声波辐射时间为5～20 min,与未进行超声波辐射处理(超声波辐射时间为0 min)相比,COD、NH3-N的去除率增加了11.37%、15.26%;超声波预处理有助于提高后续MBR对COD、NH3-N的去除作用。     

Nitrous oxide generation in denitrifying phosphorus removal process: main causes and control measures

Despite the many benefits of denitrifying phosphorus removal process, the significant generation of nitrous oxide (N₂O), a potent greenhouse gas, remains a problem for this innovative and promising process. To better understand and more effectively control N₂O generation in denitrifying phosphorus removal process, batch experiments were carried out to investigate the main causes of N₂O generation, based on which the control measures were subsequently proposed. The results showed that N₂O generation accounted for 0.41 % of the total nitrogen removal in denitrifying phosphorus removal process, whereas, in contrast, almost no N₂O was generated in conventional denitrification process. It was further demonstrated that the weak competition of N₂O reductase for electrons and the high nitrite accumulation were the two main causes for N₂O generation, evidenced by N₂O production and reduction rates under different conditions. Accordingly, the reduction of N₂O generation was successfully achieved via two control measures: (1) the use of continuous nitrate addition reducing N₂O generation by around 91.4 % and (2) the use of propionate as the carbon source reducing N₂O generation by around 69.8 %.     

Tracer-based source apportionment of polycyclic aromatic hydrocarbons in PM2.5 in Guangzhou, southern China, using positive matrix factorization (PMF)

From 28 November to 23 December 2009, 24-h?PM_2.5 samples were collected simultaneously at six sites in Guangzhou. Concentrations of 18 polycyclic aromatic hydrocarbons (PAHs) together with certain molecular tracers for vehicular emissions (i.e., hopanes and elemental carbon), coal combustion (i.e., picene), and biomass burning (i.e., levoglucosan) were determined. Positive matrix factorization (PMF) receptor model combined with tracer data was applied to explore the source contributions to PAHs. Three sources were identified by both inspecting the dominant tracer(s) in each factor and comparing source profiles derived from PMF with determined profiles in Guangzhou or in the Pearl River Delta region. The three sources identified were vehicular emissions (VE), biomass burning (BB), and coal combustion (CC), accounting for 11?±?2 %, 31?±?4 %, and 58?±?4 % of the total PAHs, respectively. CC replaced VE to become the most important source of PAHs in Guangzhou, reflecting the effective control of VE in recent years. The three sources had different contributions to PAHs with different ring sizes, with higher BB contributions (75?±?3 %) to four-ring PAHs such as pyrene and higher CC contributions (57?±?4 %) to six-ring PAHs such as benzo[ghi]perylene. Temporal variations of VE and CC contributions were probably caused by the change of weather conditions, while temporal variations of BB contributions were additionally influenced by the fluctuation of BB emissions. Source contributions also showed some spatial variations, probably due to the source emission variations near the sampling sites.     

锆(Ⅳ)负载交联壳聚糖吸附硫酸根的性能

以甲醛、苯甲醛为交联剂,制备交联壳聚糖树脂,再与锆(Ⅳ)离子反应制备锆负载交联壳聚糖吸附剂。采用静态吸附法考察了该吸附剂对水中硫酸根离子(SO24-)的吸附性能。实验发现,吸附时间2 h,SO24-溶液初始浓度500 mg/L,pH值3.0,溶液温度35℃为较优的吸附条件;吸附过程符合Langmuir等温吸附模型,属于优惠吸附型,吸附容量可达78.65 mg/g;吸附过程较好地符合拟二级动力学模型;锆负载前后交联壳聚糖对硫酸根的吸附量提高了约4.5倍;该吸附剂具有良好的耐酸性和再生性能。