沉淀--吸附处理双氯灭痛高浓度有机废水的工艺研究

介绍了用沉淀－吸附法处理双氯灭痛高浓度有机废水的工艺。先用废盐酸将废水的ｐＨ调节到４,沉淀、过滤,然后将滤液依次经过炉渣、生炭串级吸附,处理后的废水ＣＯＤＣｒ、ｐＨ、ＳＳ均达到ＧＢ８９７８－８８污水综合排放制药行业二级标准。     

用离子交换法从β盐母液中分离1-萘磺酸钠的研究

比较了Ｄ２９０、Ｄ２９６、Ｄ３０１、Ｄ３７０、Ｄ３７２、Ｄ３８０ ６种树脂对β盐母液中１－萘磺酸的静态交换性能,筛选出Ｄ２９６用以回收β盐母液中的１－萘磺酸钠,进行了ＰＨ、接触时间、交换温度等影响因素的条件试验及树脂再生试验,得到１－萘磺酸钠收率８０％以上。     

采用温度梯度凝胶电泳(TGGE)分析消毒剂对池塘型微宇宙细菌群落结构的影响

构建6个池塘型微宇宙模拟水生态系统,1个设为对照组,试验组连续投加次氯酸钠13 d,投加剂量分别为1.0、2.5、5.0、10.0、20.0 mg/L,停止投加后再观察10 d.试验期间对各微宇宙分别进行8次采样,经37 ℃培养后提取细菌总DNA,进行16S rDNA V3区扩增后,对扩增产物进行TGGE分析.对TGGE图谱中的主要条带进行回收、重新扩增、克隆、建库、测序以及序列分析.结果显示,消毒剂进入环境后会对细菌群落结构产生影响,但不同剂量消毒剂产生的影响有显著差异,存在明显的剂量-效应关系:低剂量消毒剂对细菌群落结构的影响比较小,而且是可逆的,微宇宙系统对消毒剂逐渐适应后其群落结构即可恢复;而高剂最消毒剂对细菌群落结构的破坏比较大,且不可逆转,即使消毒剂停止投加后也不能恢复.说明盲目的过量投加消毒剂会对水体微生态环境造成严重破坏.图4表1参10     

可见光/H2 O2/海藻酸铁非均相催化降解吖啶橙的研究

由海藻酸钠和氯化铁反应制备了海藻酸铁凝胶小球催化剂,考察了该催化剂的吸附和可见光下催化降解吖啶橙的性能.结果表明催化剂的吸附能力随pH升高而提高,且催化剂用量为40个凝胶小球时,可见光下吖啶橙能够在较宽pH值范围内脱色,脱色速率随H2O2的用量增加而增加,该反应符合Arrhenius规律,其表观活化能为49.6 kJ/mol.自由基清除剂的加入不会降低脱色速率,表明催化反应不是羟基自由基的机理,而与高活性的类{ Fe(Ⅳ)=O}高价铁中间产物有关.     

聚环氧琥珀酸钠阻碳酸钙垢性能研究

研究了聚环氧琥珀酸钠在不同因素下的阻碳酸钙性能。实验结果表明 ,聚环氧琥珀酸钠具有较高的阻垢性能和较好的热稳定性 ,在高钙离子浓度、高温水系统中长时间停留对碳酸钙仍有较强的抑制作用。     

Green and efficient degradation of cefoperazone sodium by Bi4O5Br2 leading to the production of non-toxic products: Performance and degradation pathway

Photocatalytic process represents a promising approach to overcome the pollution challenge associated with the antibiotics-containing wastewater. This study provides a green, efficient and novel approach to remove cephalosporins, particularly cefoperazone sodium (CFP). Bi₄O₅Br₂ was chosen for the first time to systematically study its degradation for CFP, including the analysis of material structure, degradation performance, the structure and toxicity of the transformation products, etc. The degradation rate results indicated that Bi₄O₅Br₂ had an excellent catalytic activity leading to 78% CFP removal compared with the pure BiOBr (38%) within 120 min of visible light irradiation. In addition, the Bi₄O₅Br₂ presents high stability and good organic carbon removal efficiency. The effects of the solution pH (3.12 - 8.75) on catalytic activity revealed that CFP was mainly photocatalyzed under acidic conditions and hydrolyzed under alkaline conditions. Combined with active species and degradation product identification, the photocatalytic degradation pathways of CFP by Bi₄O₅Br₂ was proposed, including hydrolysis, oxidation, reduction and decarboxylation. Most importantly, the identified products were all hydrolysis rather than oxidation byproducts transformed from the intermediate of β-lactam bond cleavage in CFP molecule, quite different from the mostly previous studies. Furthermore, the final products were demonstrated to be less toxic through the toxicity analysis. Overall, this study illustrates the detailed mechanism of CFP degradation by Bi₄O₅Br₂ and confirms Bi₄O₅Br₂ to be a promising material for the photodegradation of CFP.     

聚丙烯酸钠为结合相的薄膜扩散梯度技术对水中重金属的选择性测量

以聚丙烯酸钠(PAAS)溶液为结合相,透析膜(CDM)为扩散相,使用改进的薄膜扩散梯度(DGT)装置(CDM-PAAS-DGT),研究其对水中重金属离子累积和测量的选择性.结果表明,队AS溶液的最佳使用浓度为0.0030 mol.1-1;PAAS能够选择性的定量累积和测量水中的Cu2+(回收率98.90%)和Cd2+(回收率103.3%);PAAS与Cu2+和Cd2+的条件配位稳定常数(lgK)分别为6.98和5.61;PAAS对Cu2+和Cd2+的累积容量分别为0.416μmol·ml-1和0.498umol·ml-1.     

喹禾灵含酚废水混凝氧化效果的试验研究

选用三氯化铁作混凝剂,次氯酸钠作氧化剂,研究了混凝剂和氧化剂的投加量、pH及不同的反应时间对喹禾灵含酚废水处理效果的影响。试验结果表明,混凝剂最佳投加量为8．0g／L,最佳pH为9～10;氧化剂最佳投加量为50mL/L(有效氯为5．2％)．最佳pH为2～3。在最佳条件下,废水经混凝氧化后,其CODc,、对苯二酚、色度的去除率分别达98．12％、97．26％、99．00％。     

腐殖酸钠和表面活性剂对黄土中石油污染物解吸增溶作用

选用十二烷基苯磺酸钠(LAS)、十二烷基硫酸钠(SDS)和十二烷基磺酸钠(SAS)对污染的土壤进行解吸实验,研究了这3种阴离子表面活性剂和腐殖酸钠对黄土中柴油类污染物的协同增溶作用.结果表明,腐殖酸钠和3种阴离子表面活性剂对黄土中柴油的解吸均有显著增溶作用,使柴油的解吸量明显增加,柴油的去除率最高可达63%.SDS对柴油的解吸量随腐殖酸钠浓度增大呈线性增加关系;但腐殖酸钠浓度增加对 LAS和SAS的解吸曲线有突越点,超过此浓度后反而会抑制解吸作用.     

Oxidation inhibition of sulfite in dual alkali FGD system

A laboratory-scale well-mixed thermostatic reactor with continuously blasting air was used to investigate the oxidation inhibition of sulfite in dual alkali flue gas desulfurization （FGD） system. The effects of operating parameters such as pH value and catalyst concentration on the oxidation were studied. Sodium thiosulfate was used in the system, and was found that it significantly inhabited the sulfite oxidation. In the absence of catalyst, sodium thiosulfate at 12.67 mmol/L had an inhibition efficiency of approximately 98%. While in the presence of catalyst, sodium thiosulfate at 26.72 mmol/L had an inhibition efficiency less than 85.0%. The oxidation reaction order of sulfite in the sodium thiosulfate was determined to be -1.90 and 4）.55 in the absence and presence of the catalyst, respectively. Apparent activation energy of oxidation inhibition was calculated to be 53.9 kJ/mol. Pilot tests showed that the consumption rate of thiosulfate agreed well with the laboratory-scale experimental results.