共查询到18条相似文献，搜索用时 375 毫秒
1.
以坡缕石粘土、淀粉、水玻璃为原料,研究了固定化酶载体的制备工艺,探究了固定化酶载体在辣根过氧化酶(HRP)降解硝基酚废水中的作用,并探讨了反应时间、酶浓度、H2O2及硝基酚浓度对降解效果的影响。结果表明,固定化酶载体的最佳制备工艺为:水玻璃12%,淀粉20%,煅烧温度550℃,煅烧时间2 h;固定化酶对硝基酚的去除效果明显高于原酶;固定化酶去除水中硝基酚的最佳反应条件为:反应时间1.5 h,加酶量150 U,H2O2浓度0.12%,硝基酚浓度100 mg/L;固定化酶重复使用7次后对硝基酚的去除率仍高于60%。 相似文献
2.
《地学前缘》2012,6(3)
以蒙脱土为载体制备负载型Fe/Al复合氧化物（FeAlOx/MMT）用于催化Fenton反应降解高浓度苯酚废水。实验结果表明,活性相FeAlOx中Fe/Al摩尔比为0.22时制备所得催化剂对Fenton反应具有最佳活性,且Fe/Al复合氧化物并未嵌入蒙脱土层间。在低温和高pH条件下催化体系存在诱导期,诱导期内FeAlOx/MMT缓释出Fe离子并进而由Fe离子催化溶液中的Fenton反应。通过对非均相催化降解苯酚废水的动力学研究发现,H2O2初始浓度、溶液的pH和反应温度对COD降解效率具有显著影响。调节降解过程中的温度序列和氧化剂引入程序能够缓解高温和高双氧水浓度双重因素耦合导致的HO.自消耗。在优化的降解条件下使用理论用量的H2O2可使得1 g/L的苯酚废水中苯酚降解率达到100%,而COD的降解率则达到97%。 相似文献
3.
为研究双金属催化剂去除有机污染物的效果,采用自制Fe/Ag催化剂对模拟苯酚废水进行了臭氧催化氧化处理。通过扫描电子显微镜(SEM)、比表面积分析仪(BET)和X射线衍射(XRD)对催化剂进行表征,并考察了催化剂类型、催化剂投加量和溶液初始pH值对降解效果的影响规律。结果表明:与Fe相比,Fe/Ag比表面积减少了22.8%,在Fe/Ag/O3与含苯酚废水的反应体系中,反应遵循臭氧直接作用和活性自由基(·OH、·O2、H2O2)共同作用的机理;Fe/Ag在反应过程中体现出良好的协同作用;300 mg/L的苯酚模拟废水在pH=6.3、Fe/Ag投加量为1.00 g的最优反应条件下经60 min反应,苯酚与化学需氧量(COD)去除率比单独臭氧氧化分别提高了18.4%和29.4%。 相似文献
4.
采用酸性溶胶法制备掺铁-TiO2/膨润土复合光催化剂,利用XRD﹑IR等测试手段对其进行了表征。通过测试甲基橙溶液的脱色率和COD去除率对复合光催化剂的光催化活性进行了评价。结果表明,该催化剂有较高的催化氧化性能,在太阳光照射下,对pH=4﹑质量浓度为20 mg/L的甲基橙溶液进行降解时,其脱色率可达95%以上,COD去除率可达85%以上。该催化剂在经过200℃焙烧活化2.5 h后可多次重复利用。 相似文献
5.
地下水中三氯乙烯-苯酚的好氧共代谢的实验研究 总被引：4，自引：1，他引：3
以苯酚作为三氯乙烯（TCE）降解的共代谢基质,用瓦勃氏微量呼吸测压仪（简称瓦呼仪）作为测试手段,分析了经苯酚驯化后的混合微生物对苯酚、TCE的降解特性;并讨论了以苯酚作为共代谢基质时TCE降解的可能性。实验结果表明：未驯化的活性污泥不能降解TCE; 经苯酚驯化后的活性污泥,当TCE的质量浓度为50 μg/L时其降解效果较好,TCE的氧化率达3369%;TCE的质量浓度为100 μg/L时其降解效果较差,其氧化率仅为3.2%;苯酚和TCE共代谢降解时,苯酚的存在促进了TCE的降解,当苯酚质量浓度为40 mg/L、TCE质量浓度为50 μg/L时共代谢降解效果最好,TCE的氧化率为79.11%。 相似文献
6.
固定化酶在高浓度有机废水处理中的应用 总被引：11，自引：2，他引：9
选用硅胶、活性炭、大孔树脂三种载体,在一定条件下用物理吸附法固定蛋白酶,三种载体固定的蛋白酶对含高浓度蛋白质的淀粉黄浆废水进行水解实验,确定水解最佳的pH值范围,并在此条件下研究三种不同载体上固定化酶的活性及其水解规律。结果表明：大孔树脂对蛋白酶的固定效果良好,并对含高浓度蛋白质的废水处理效果最好,其最佳反应pH值为5.5,反应进行0.5 h时酶的催化效果最好,氨基酸产生速度达到30.82 mg/min,且在3h后该速度仅减少3.74 mg/min;6 h时对蛋白质的去除率达到39.93%。 相似文献
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利用交互正交试验设计对柠檬酸络合法制备Mn/Ce复合氧化物催化剂(简称Mn/Ce催化剂)的制备条件进行了优化,重点考察金属配比(Mn∶Ce=7∶3、1∶1、3∶7)、焙烧温度(350℃、500℃、650℃)、焙烧时间(2 h、3.5 h5、h)等3种因素对催化湿式氧化(CWAO)降解正丁酸过程中Mn/Ce催化剂活性的影响。结果表明,金属配比和焙烧温度对催化剂活性有显著影响(置信度p分别为99%和95%),焙烧时间对催化剂活性无显著影响(p=90%),焙烧温度与金属配比之间有显著的交互作用(p=99%),得到的最佳制备条件为:Mn∶Ce=3∶7、焙烧温度500℃和焙烧时间5 h;并对最佳制备条件下得到的Mn/Ce催化剂进行XRD、BET和SEM等表征。 相似文献
9.
采用电-Fenton法对含苯酚废水进行处理,以石墨为阴极、铁为阳极,并向阴极不断通入空气,电解过程产生的H2O2与阳极溶解的Fe^2＋形成Fenton试剂,Fenton试剂在电解过程中产生大量活性羟基自由基,能够很好地氧化降解废水中的苯酚。实验结果表明：影响苯酚去除率的因素主次顺序为pH值、电解质浓度、电解电压、电解时间、进水苯酚浓度。单因素分析得出电-Fenton法处理苯酚模拟废水的最优反应条件：pH值控制在2左右,反应时间为60min,电解电压选10V,Na2SO4的浓度为30g／L,进水苯酚浓度为150mg／L。在最优条件下苯酚的去除率为82％。 相似文献
10.
探讨了人工合成的高价锰氧化物与紫外光(UV)联用时降解苯酚废水的特性。结果表明,氧化锰矿物在无UV时对苯酚的降解能力差异大,1 g/L的氧化锰4 h对200 mg/L苯酚废水的降解率和COD去除率分别为:锰钾矿97.51%、酸性水钠锰矿89.07%、碱性水钠锰矿11.36%、钙锰矿9.67%;锰钾矿87.79%、酸性水钠锰矿53.11%、碱性水钠锰矿6.42%、钙锰矿1.43%。UV光照下,氧化锰矿物对苯酚的降解率有不同程度的提高,且表现出显著的表面光催化性质,增加了苯酚的深度降解,COD去除率显著提高。UV下氧化锰4 h对苯酚的降解率分别为:锰钾矿99.48%、酸性水钠锰矿91.86%、碱性水钠锰矿40.15%、钙锰矿35.95%);COD的去除率分别为:锰钾矿98.11%、酸性水钠锰矿68.45%、钙锰矿27.57%、碱性水钠锰矿24.27%。MnO2-UV联用时降解苯酚可能包括两种主要作用机制:氧化锰矿物的直接化学氧化降解和UV下MnO2的表面光催化降解。 相似文献
11.
M. Zeinali H. Lenjannezhadian 《International Journal of Environmental Science and Technology》2018,15(1):49-56
Urease which catalyzes biodegradation of urea to ammonia and carbon dioxide has attracted a great deal of attention as a catalyst in food industry, agriculture and artificial kidneys. Immobilization is a unique approach for enhancement of enzyme stability before enzyme industrialization. In the present work, crude sword bean urease was immobilized in the form of cross-linked enzyme aggregate prior to entrapment in polyacrylamide gel or chitosan beads. No significant change was observed in the kinetic constant value (k m ) of urease upon formation of cross-linked enzyme aggregate. Entrapment of urease cross-linked aggregates in chitosan beads resulted in complete loss of activity while polyacrylamide-embedded cross-linked urease aggregates were enzymatically active. The optimum temperature for urease was 60 °C (soluble and cross-linked aggregate form) and 70 °C (polyacrylamide-embedded cross-linked aggregate). The optimal pH for urease was 7.0 (soluble and cross-linked aggregate form) and 5.0 (polyacrylamide-embedded cross-linked aggregate). In the other words, immobilization in the form of cross-linked aggregate and entrapment in polyacrylamide matrix could be resulted in the stabilization of urease over a wider pH range. Urease cross-linked aggregate showed improved stability at 60 °C, and its half-life increased about two times. Operational stability of cross-linked urease aggregate was also noticeably improved upon entrapment in polyacrylamide gel. In conclusion, entrapment of carrier-free cross-linked urease aggregate in a polyacrylamide matrix could result in a great improvement in both the storage and operational stabilities of urease. 相似文献
12.
Enhancement of atrazine degradation by crude and immobilized enzymes in two agricultural soils 总被引：1，自引：0，他引：1
Tingting Ma Lusheng Zhu Jinhua Wang Jun Wang Hui Xie Jun Su Qingming Zhang Bo Shao 《Environmental Earth Sciences》2011,64(3):861-867
Contamination of soil, groundwater and surface water by atrazine is a worldwide concern. Arthrobacter sp. HB-5 is a high-efficiency atrazine degradation strain isolated by our laboratory. Crude enzyme extracted from HB-5 and immobilized
enzyme made from crude enzyme on sodium alginate were introduced to atrazine-polluted soils to evaluate the degrading ability
for practical use and to calculate the kinetics of atrazine degradation. Atrazine was applied at 10 mg/kg of soil. Brown soil
or cinnamon soil samples with crude or immobilized enzyme were incubated at 25°C. Samples were collected every 24 h from 0
to 144 h to extract the residual atrazine and analyzed using gas chromatography. Results showed, at 144 h, that only about
10% of the initially applied amount of atrazine was left in the two soils, except in the control soil samples without crude
or immobilized enzyme. Before 48 h of incubation, crude enzyme removed atrazine faster than the immobilized enzyme in each
soil sample. However, after 120 h, degradation of atrazine reached a similar level with either treatment. Atrazine seemed
to be removed more easily from cinnamon soil than from brown soil, and both crude and immobilized enzyme could be used. However,
the immobilized enzyme is preferred for its stability. 相似文献
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M. Sogani N. Mathur P. Bhatnagar P. Sharma 《International Journal of Environmental Science and Technology》2012,9(1):119-127
Amidase hydrolases/acyltransferases are of considerable industrial interest due to potential applications in the production of useful hydroxamic acids. The test strain, capable of acetamide degradation, was isolated by an enrichment technique with acetamide as sole source of nitrogen. Based on morphology, physiological tests and biochemical tests, this isolate was identified as Bacillus sp. and on the basis of 16S Ribosomal ribonucleic acid sequence, a phylogenetic tree was drawn and was identified as Bacillus megaterium. Resting cells containing active acyltransferase enzyme were prepared and immobilized in the gel beads of sodium alginate, agar, polyacrylamide and polyvinyl alcohol?Calginate. The beads were tested for acyltransferase using Iron (III) chloride reagents at 55°C and were found to be affected by substrate concentration, type of buffer, buffer pH and reaction temperature. These factors were optimized using sodium alginate immobilized beads. This study proved useful in understanding the technique of immobilization of acyltransferase enzyme, its operational stability and its importance in the synthesis of hydroxamic acid. 相似文献
14.
X. J. Gao X. J. Fan X. P. Chen Z. Q. Ge 《International Journal of Environmental Science and Technology》2018,15(10):2203-2212
The emergence of antibiotics residues in pharmaceutical industrial wastewater has been a significant environment problem. However, current methods of treating antibiotic-polluted wastewater are inefficient, of high cost and time-consuming. In this study, highly effective enzymatic Fe3O4 magnetic nanoparticles were developed, which is extremely simple and can degrade antibiotics in a fast manner at a low cost. β-Lactamase, a representative enzyme for β-lactam antibiotic degradation, was covalently immobilized on the surface of magnetic nanoparticles modified with amino groups by a simple cross-linking process. The immobilized β-lactamase displayed a wider pH and temperature range for penicillin G degradation than the free enzyme. Meanwhile, the thermostability and storage stability of the immobilized β-lactamase were improved. Fifty milligrams magnetic nanoparticles immobilized with β-lactamase can thoroughly degrade 100 mL penicillin G (5–50 mg L?1) within 5 min. Even if the β-lactamase immobilized on the nanoparticles was reused 35 times in the 5 mg L?1 penicillin G solution, it still kept more than 95% degradation efficiency. These suggest that magnetic nanoparticles immobilized with β-lactamase have a sufficient capacity for degrading antibiotics in wastewater and will serve as a practical and economical solution to antibiotic pollution in pharmaceutical industrial wastewater treatment. 相似文献
15.
Hong-Yan Zeng Xiao-Li Cao Long-Bin Xiong Xi-Ling Cai Li-Qun Huang Cun-Ying Zhang Yu-Qin Li 《Environmental Earth Sciences》2014,71(3):1339-1348
Phenol biodegradation in an aerobic batch reactor was investigated using mixed two co-aggregating strains (Flavobacterium sp. and Acetobacter sp.). Response surface methodology by the Box–Behnken model was used to evaluate the optimal cell growth and phenol degradation conditions. The optimum temperature, pH value and inoculum size were found to be 33 °C, 6.06 and 13 %, respectively. In the conditions, phenol degradation rate and biomass were predicted to be 96.97 % and 410.78 mg/L within the range examined, respectively. Less toxic acetaldehyde, ethanol and acetic ether were identified as main intermediate products from the degraded samples using GC–MS. Substrate inhibition was calculated from experimental biomass growth and phenol degradation parameters using the Haldane equation. Kinetic parameters derived from nonlinear regression with correlation factors (R 2) were 0.9682 for phenol degradation and 0.9594 for biomass growth, respectively. The phenol concentration to avoid substrate inhibition was 278.17 mg/L. 相似文献
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针对我国东北某石油烃污染场地地下水中的萘污染,筛选出了Acinetobacter和Pseudomonas菌属的高效萘降解菌群。该菌群对萘的耐受性较高,且具有良好的乳化性,能够自动调节细胞表面疏水性和自聚集性。不同pH值、萘初始浓度、温度和菌接种量对萘降解效率的影响研究表明:最适菌群生长的pH范围为7.08.0;萘降解效率和速率在1.005.00 mg/L范围内与其初始浓度成正比;在1030 ℃温度范围内均表现出较高的萘降解效率。在此基础上,利用Guass、GuassAmp、LogNomal、Poisson和Pulse数学模型对萘的降解过程进行拟合,其降解速率更符合GuassAmp模型。通过将降解动力学模型中的常数与影响因素相关联,推导出了拟合度较高的多因素影响下的萘降解动力学方程。 相似文献
18.
为了考察铁锰氧化物对酚类污染物的氧化降解能力,采用天然以及合成的铁锰氧化物对苯酚的氧化降解进行对比实验研究。土壤中铁锰氧化物样品分别为天然针铁矿及氧化锰,合成铁锰氧化物样品分别为合成针铁矿及软锰矿。结果表明：苯酚与铁锰氧化物发生氧化还原作用时,还可能与土壤中杂质发生吸附等作用;铁锰氧化物还原反应强度随着反应介质pH值的升高而迅速下降;可用零级反应动力学方程拟合铁氧化物还原溶解反应,针铁矿溶解反应的强度与介质的pH值呈负相关关系;天然针铁矿对酚类污染物的氧化降解能力明显高于合成针铁矿,pH值对天然针铁矿溶解反应影响较大;可用一级指数衰减方程拟合锰氧化物还原溶解反应,锰氧化物溶解反应的强度与介质的pH值呈指数衰减关系;pH值对软锰矿还原溶解反应的影响大于对土壤中氧化锰的影响,pH值越小,影响越显著;对比pH值对铁和锰还原作用的影响发现,在pH=6.5时,锰氧化物仍有较强的氧化性能。 相似文献