无硫膨胀石墨的制备及吸油性能

通过单因子实验考察了无硫膨胀石墨制备过程中氧化剂及插层剂用量、氧化反应及插层反应时间、氧化反应及插层反应温度对无硫膨胀石墨膨胀体积的影响。通过正交实验确定了制备无硫膨胀石墨的最优条件是:石墨(g)∶浓硝酸(mL)∶30%H2O2(mL)∶乙酸酐(mL)=1∶2.25∶0.25∶0.6,在30℃条件下氧化反应60 min,加入插层剂后在60℃条件下插层反应90 min,此条件无硫膨胀石墨的膨胀体积达317 mL/g使用XPS、FT-IR、XRD和SEM对无硫膨胀石墨进行了表征并对其吸油性能和再生性能进行了研究。结果表明,所制备无硫膨胀石墨对原油和柴油的最大吸附量分别为66.3 g/g和62.7 g/g。吸附原油后的无硫膨胀石墨抽滤再生后首次再生率为49.1%,原油的回收率为64.5%。     

利用剩余活性污泥生产一次性可降解材料

为了缓解污水处理厂日益严重的污泥处置难题,实现剩余活性污泥的无害化、减量化、稳定化、资源化利用。采用SBR系统对剩余活性污泥进行10 d的驯化,加入4.0 g/L的乙酸钠作为发酵培养基碳源和前体物质,累积聚羟基烷酸酯(polyhydroxyalkanoates,PHA)。30℃好氧发酵10 h后,PHA积累达1 125 mg/L,占污泥浓度(MLSS)的质量分数为35.7%。然后经过离心、烘干、粉碎后模压成型加工成一次性使用的可生物降解材料。使用正交实验进行优化,结果表明:其最佳的物料配比和模压条件为:干污泥57%;稻草纤维20%;聚乙烯醇(PVA)19%;硬脂酸钡2%;氧化钙2%;最佳工艺条件为100℃,加热1.5 h,此时加工出来的产品具有最优的抗压强度和拉伸强度。以本方法制成的可生物降解花盆其所含细菌总数、粪大肠菌群、蛔虫卵死亡率均达到国标所规定的污泥农用生物安全要求;另外,试样中未检出病毒;其重金属含量也达到国标所规定的污泥农用标准;其可生物降解性能达到了可降解材料的要求。因而本研究制备的一次性使用可降解花盆具有较好的开发和应用价值。     

Fenton 法降解抗生素磺胺间甲氧嘧啶钠

应用Fenton高级氧化技术降解水溶液中抗生素磺胺间甲氧嘧啶钠(SMMS),系统探讨了起始pH、CSMMS、CFe2+、CH2O2和温度等因素对SMMS降解效果的影响。结果表明:CSMMS=4.53 mg/L,pH=4.0,CH2O2=0.49 mmol/L,CFe2+=19.51μmol/L,T=25℃为最佳反应条件。在最佳条件下,87.4%的SMMS可以在120 min内降解。反应动力学研究表明Fenton氧化降解SMMS分为两个阶段,快速反应阶段和慢速反应阶段,并建立了两阶段动力学模型,模型拟合结果较好。研究结果为含有SMMS的污废水处理提供了基础数据和科学参考。     

Spatial and temporal variations and possible sources of dichlorodiphenyltrichloroethane (DDT) and its metabolites in rivers in Tianjin, China

Water, suspended solid (SS) and sediment samples were collected from nine water courses in Tianjin, China and analyzed for dichlorodiphenyltrichloroethane (DDT) and its metabolites (DDXs, including o,p'-,p,p'-DDT, DDD and DDE). The average DDX concentrations in water, SS and sediment were 59+/-30 ng l(-1), 2690+/-1940 ng g(-1)dry wt. and 340+/-930 ng g(-1)dry wt., respectively. Due to the termination of the extensive agricultural application and industrial manufacture, DDXs in river sediment decreased by one order of magnitude since 1970's and low DDT fractions in these sediments were observed. Still, DDXs in the sediments near the outlets of the major manufacturers remained relatively high attributed to the historic input. DDXs in sediment were also positively correlated with organic matter content. Spatial distributions of DDXs in SS and water was different from that in sediment. For SS, a negative correlation between DDX concentration and SS content indicated a dilution effect in many rivers. Dissolved organic carbon content was the major factor affecting DDX concentrations in water phase. Wastewater discharged from dicofol manufacturers and likely illegal agricultural application were the primary reasons causing high DDT (DDE+DDD) ratios in SS and water.     

污水厂Carrousel氧化沟溶解氧和速度分布的研究

对长沙某污水处理厂的Carrousel氧化沟进行现场测试，获得不同截面的溶解氧和速度的数据，探讨了表曝机台数、沟深、沟的长宽比、进出水位置对溶解氧和速度的影响。初步掌握了该Carrousel氧化沟内溶解氧和速度的变化规律，认为通过调节倒伞形表面曝气机，可以在沟内不同区段创造好氧与缺氧的环境，为最终实现同步硝化反硝化的高效运行做准备。     

石英砂负载氧化铁吸附除磷的热动力学研究

通过吸附动力学实验及等温吸附实验,考察了在10～40℃的温度条件下石英砂负载氧化铁(IOCS)吸附磷的热动力学性质.结果表明:准二级反应动力学模型及Langmuir等温吸附模型可分别较好地描述IOCS对磷的吸附动力学及吸附等温线实验结果(R2≥0.98);吸附速率及吸附容量随温度的增加而增加.吸附速率k从0.0095增加到0.0173,吸附容量从0.06 mg/g增加到0.08 mg/g.根据标准吉布斯自由能变(△G0＜0)和标准反应焓变(△H0＞0)值判断,IOCS对磷的吸附是自发的、吸热的化学吸附反应.     

Ti/Cu交联累托石光催化氧化处理硝基苯废水研究

以钛酸丁酯为钛源,掺杂铜(CuCl2)制备交联剂.制得柱状Ti/Cu交联累托石,结合其吸附特性并通过其在光催化氧化条件下处理含硝基苯有机废水.在pH=9,交联累托石用量为30 g/L,一根20 W紫外灯光辐照2 h的处理条件下,硝基苯由73.81 mg/L降至3.17 mg/L,去除率达到95.71%,优于GB-8978-1996三级标准,用其处理含硝基苯工业废水,COD去除率为83.73%,由4800 mg/L降至530.4 mg/L,硝基苯去除率达92.3l%,由10.32 mg/L降至0.79 mg/L,小于GB-8978-1996-级标准.     

Distribution of elements in needles of Pinus massoniana (Lamb.) was uneven and affected by needle age

Macronutrients (P, S, K, Na, Mg, Ca), heavy metals (Fe, Zn, Mn, Cu, Pb, Cr, Ni, Cd,) and Al concentrations as well as values of Ca/Al in the tip, middle and base sections, and sheaths of current year and previous year needles of Pinus massoniana from Xiqiao Mountain were analyzed and the distribution patterns of those elements were compared. The results indicated that many elements were unevenly distributed among the different components of needles. Possible deficiency of P, K, Ca, Mn and Al toxicity occurred in needles under air pollution. Heavy metals may threaten the health of Masson pine. Needle sheaths were good places to look for particulate pollutants, in this case including Fe, Cu, Zn, Pb, Cr, Cd and Al.     

催化湿式氧化技术处理山梨酸生产废水的研究

采用催化湿式氧化技术处理生产山梨酸过程中产生的高浓度有机废水,对催化剂组分进行优选.对反应温度、O2分压(Po2)和废水pH等工艺条件进行考察.实验结果表明:采用自制CuO-Cr2O3-La2O3/TiO2为复合催化剂处理该有机废水时表现出较好的催化活性;在190℃、Po2=2.1 MPa、pH=6.1、COD=10 030.0 mg/L时,反应90 min的COD去除率达到98.3%,而在相同条件下未加催化剂的湿式氧化的COD去除率只有60.1%.     

Perfluorinated compounds in the Pearl River and Yangtze River of China

A total of 14 perfluorinated compounds (PFCs) were quantified in river water samples collected from tributaries of the Pearl River (Guangzhou Province, south China) and the Yangtze River (central China). Among the PFCs analyzed, perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) were the two compounds with the highest concentrations. PFOS concentrations ranged from 0.90 to 99 ng/l and <0.01–14 ng/l in samples from the Pearl River and Yangtze River, respectively; whereas those for PFOA ranged from 0.85 to 13 ng/l and 2.0–260 ng/l. Lower concentrations were measured for perfluorobutane sulfonate (PFBS), perfluorohexane sulfonate (PFHxS), perfluorooctanesulfoamide (PFOSA), perfluorohexanoic acid (PFHxA), perfluoroheptanoic acid (PFHpA), perfluorononaoic acid (PFNA), perfluorodecanoic acid (PFDA), and perfluoroundecanoic acid (PFUnDA). Concentrations of several perfluorocarboxylic acids, including perfluorododecanoic acid (PFDoDA), perfluorotetradecanoic acid (PFTeDA), perfluorohexadecanoic acid (PFHxDA) and perfluorooctadecanoic acid (PFOcDA) were lower than the limits of quantification in all the samples analyzed. The highest concentrations of most PFCs were observed in water samples from the Yangtze River near Shanghai, the major industrial and financial centre in China. In addition, sampling locations in the lower reaches of the Yangtze River with a reduced flow rate might serve as a final sink for contaminants from the upstream river runoffs. Generally, PFOS was the dominant PFC found in samples from the Pearl River, while PFOA was the predominant PFC in water from the Yangtze River. Specifically, a considerable amount of PFBS (22.9–26.1% of total PFC analyzed) was measured in water collected near Nanjing, which indicates the presence of potential sources of PFBS in this part of China. Completely different PFC composition profiles were observed for samples from the Pearl River and the Yangtze River. This indicates the presence of dissimilar sources in these two regions.