酚酸类化合物各基团对土壤中氮的硝化作用的影响

本文观察到酚酸类化合物分子中的酚羟基对土壤中氮硝化有关的微生物及酶具有毒性作用,是抑制土壤中氮硝化作用的主要影响基团。羧基或羧乙烯基对酚羟基抑制硝化作用的影响有一定的抵消作用,其中羧乙烯基的抵消作用更强。由于这一抵消作用,本文中七种酚类化合物对土壤中氮硝化作用的抑制总的来说是微弱的。     

组合工艺处理高浓度酚醛废水的研究

针对绝缘材料厂酚醛树脂生产废水高酚高醛的水质特点，研究了二次缩合-化学氧化-粉煤灰吸附组合处理工艺。结果表明，经该工艺处理后不仅出水酚含量可降至0．3mg／L以下，CODCr10．2mg／L左右，各项水质指标均达到了GB8978—96污水综合排放一级标准，同时还可回收一定数量的树脂。     

Enhanced photodegradation of phenolic compounds by adding TiO2 to soil in a rotary reactor

Photodegradation ofpentachlorophenol （PCP） and p-nitrophenol （PNP） in soil was carried out in a designed rotary reactor, which can provide the soil particles with continually uniform irradiation, and on a series of thin soil layers. TiO2, as a kind of environmental friendly photocatalyst, was introduced to the soil to enhance the processes. Compared with that on the soil layers, photodegradation of PCP at initial concentration of 60 mg/kg was improved dramatically in the rotary reactor no matter whether TiO2 was added, with an increase of 3.0 times in the apparent first-order rate constants. The addition of 1 wt% TiO2 furthered the improvement by 1.4 times. Without addition of TiO2, PNP （initial concentration of 60 mg/kg） photodegradation rate in the rotary reactor was similar to that on the soil layers. When 1 wt% additional TiO2 was added, PNP photodegradation was enhanced obviously, and the enhancement in the rotary reactor was 2 times of that on the soil layers, which may be attributed to the higher frequency of the contact between PNP on soil particles and the photocatalyst. The effect of soil pH and initial concentrations of the target compounds on the photodegradation in the rotary reactor was investigated. The order of the degradation rate at different soil pH was relative to the aggregation of soil particles during mixing in the rotary reactor. Photodegradation of PCP and PNP at different initial concentrations showed that addition of TiO2 to enhance the photodegradation was more suitable for contaminated soil with higher concentration of PCP, while was effective for contaminated soil at each PNP concentration tested in our study.     

新型溴代苯酚类消毒副产物的氯化降解机制

最近,13种新型极性卤代苯酚类消毒副产物在氯化消毒后的饮用水中被发现,它们按结构被分成4组,分别是二卤-4-羟基苯甲醛、二卤-4-羟基苯甲酸、二卤水杨酸和三卤苯酚.为研究它们在氯化消毒过程中的降解机制,选取了其中的4种全溴代种类,即3,5-二溴-4-羟基苯甲醛、3,5-二溴-4-羟基苯甲酸、3,5-二溴水杨酸以及2,4,6-三溴苯酚,利用UPLC/ESI-tq MS中的前体离子扫描,多反应监测和子离子扫描,鉴定了这几种消毒副产物在氯化消毒过程中的中间产物以及终产物,并根据这些中间产物和终产物与消毒时间的关系推测了其降解路径.结果表明,除了3,5-二溴水杨酸相对较稳定外,其余3种消毒副产物在氯化消毒过程中不稳定,通过取代、水解以及氧化等过程最终降解为卤乙酸等脂肪族小分子消毒副产物.在降解过程中有许多中间产物被检测并鉴定出来,其中包含一组具有五元环结构的新型消毒副产物(三卤代-羟基环戊烯二酮).     

均相阳离子隔离阴阳极室电化学降解含酚废水实验及其动力学研究

在隔离阴阳极室的条件下进行电化学法降解含酚废水实验 ,结果表明 ,在 2 5～ 4 5℃的低温范围内 ,苯酚的转化率能达到 95 %以上。反应动力学研究揭示 ,其活化能Ea =12 75～ 16 0 6kJ mol,与一般化学反应的活化能Ea =6 0～2 5 0kJ mol相比 ,本实验的活化能很低 ,即反应所要克服的势能垒很低 ,反应更易进行 ,这是电化学脱酚速率快 ,降解彻底的重要原因 ;另外 ,不同电解液对比实验显示 ,降解苯酚时在碱性电解液中更为有效     

CeO2形貌结构对催化湿式空气氧化苯酚性能的影响

采用水热法、沉淀法和溶胶凝胶法制备了3种不同形貌的CeO₂催化材料,并将其用于湿式空气氧化苯酚水溶液过程中,探讨了CeO₂形貌结构对催化湿式氧化苯酚水溶液性能的影响.采用扫描电子显微镜（SEM）、透射电子显微镜（TEM）、X射线衍射（XRD）、程序升温还原（TPR）等手段对CeO₂催化材料进行了表征.结果表明,水热法制备的CeO₂催化材料表现出较好催化性能,主要原因是水热法合成的CeO₂呈现交错的纳米棒状结构,主要暴露（220）晶面,且沿着（220）晶向生长.在反应温度为200℃、空气压力为2MPa、苯酚初始浓度500mg/L的条件下,最终（240min）COD的去除率为95.5%.     

酚类化合物的HPLC测定

本文研究了酚类化合物的HPLC的测定条件:组装HPLC仪器包括:LKB2150高压泵,日立635M多波长检测器,UV—210和UV280nm,日本U—225M双笔记录仪。分离拄:500mm×2.6mm不锈钢,内填日立2618~#树脂。流动相:0.05％磷酸。流量0.015L/h～0.024 L/h。泵压:12000000～14000000Pa。进样量:0.0025～0.01ml。对苯酚,间苯三酚,邻苯三酚,邻苯二酚,对苯二酚,乙萘酚,邻甲酚,间甲酚等进行了分离测定。方法简易,灵敏度高,重复性好。     

UV-Fenton氧化-生化法联合处理含酚废水

采用UV-Fenton氧化-生化法联合处理煤气含酚废水,比较了单独UV-Fenton氧化法、单独生化法和UV-Fenton氧化-生化法联合工艺对煤气含酚废水的处理效果.结果表明,UV-Fenton氧化体系可有效降解含酚废水,但废水完全降解所需的H2O2用量大,处理成本高.煤气含酚废水的BOD5/COD比值较低,直接采用...     

Tyrosinase-modified carbon felt-based flow-biosensors: The role of ultra-sonication in shortening the enzyme immobilization time and improving the sensitivity for p-chlorophenol

Tyrosinase (TYR) was covalently immobilized onto amino-functionalized carbon felt surface via glutaraldehyde-coupling under ultrasonic treatment for 10 min. The resulting TYR-immobilized carbon felt was used as a working electrode unit of bioelectrocatalytic flow-through detector for TYR substrates (catechol, p-chlorophenol (p-CP), p-cresol, phenol etc.). Cathodic peak currents based on the electroreduction of enzymatically produced o-quinones were detected at –50 mV vs. Ag/AgCl. Compared with previous work in which TYR was immobilized onto amino-functionalized carbon felt for 16 hr without the ultrasonic treatment, we succeeded in (1) shortening the enzyme immobilization time from 16 hr to 10 min, (2) enhancing the sensitivity of p-CP, and (3) improving the operational stability of p-CP. The ultrasonic treatment during the TYR immobilization step would lead to certain changes in the structure of the immobilized TYR and the morphology of the immobilized TYR-layer on the carbon felt surface.     

膜生物反应器处理高浓度含酚废水研究

将膜生物反应器(MBR)用于高浓度含酚废水的处理中,探讨了进水中苯酚浓度、水力停留时间和污泥浓度对膜生物反应器处理含酚废水效果的影响。实验结果表明:经过42d驯化后,可以在高浓度含酚废水中正常运行,MBR系统对COD和氨氮的去除率分别可达98%和80.6%。当苯酚浓度为134mg/L时,处理的最佳水力停留时间为3h,最佳污泥浓度(MLSS)为7367mg/L。