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1.
臭氧-超声联用处理聚乙烯醇废水   总被引：2，自引：0，他引：2  
本研究采用臭氧-超声（O3/US）联用技术处理聚乙烯醇（PVA）废水,分别考察了PVA初始质量浓度、初始pH、臭氧通入速率、超声功率、超声频率及反应时间对PVA和COD去除效率的影响,并在此基础上通过正交实验确定了降解PVA和COD的最佳实验条件。研究结果表明,超声频率对去除率有显著影响,PVA初始质量浓度对去除效率的影响较大,反应时间、超声功率、臭氧通入速率和初始pH的影响相对较小。通过影响实验和正交实验确定的最佳降解条件为:PVA初始质量浓度100 mg/L、初始pH=9、臭氧通入速率4 g/h、超声功率320 W、超声频率40 kHz、反应时间20 min,此时COD和PVA的去除效率分别为86.4%和99.3%。超声对臭氧降解聚乙烯醇废水具有明显的协同作用,在最佳条件下,臭氧-超声联用技术比单独臭氧技术对PVA的去除率增加了5.1%,对COD去除率增加了19.4%。  相似文献   

2.
为了进一步研究氮掺杂碳材料活化过硫酸盐降解4-氯苯酚的方法,首先以廉价易得的废弃工业糖浆作为碳源,以氨水作为氮源,利用溶胶-凝胶法合成了3种氮掺杂碳材料（NC-700,NC-800和NC-900）,并利用扫描电子显微镜（SEM）、X射线衍射（XRD）、拉曼光谱（Raman）、X射线光电子能谱（XPS）等技术对氮掺杂碳材料进行表征分析;然后考察了NC-800投加量、过硫酸盐（PDS）投加量和初始pH等因素对4-氯苯酚去除率的影响,并进行了电子自旋共振（ESR）和自由基淬灭实验。结果表明：3种材料均可有效活化PDS降解4-氯苯酚,其中NC-800活化PDS去除4-氯苯酚效率最高;当NC-800投加量为100 mg/L、PDS投加量为5 mmol/L时,反应30 min后,50 mg/L的4-氯苯酚的总去除率达99.10%;初始pH对4-氯苯酚去除率无明显影响;NC-800活化过硫酸盐降解4-氯苯酚遵循非自由基途径,单线态氧为降解4-氯苯酚的活性物质。循环使用实验证明NC-800具有一定的稳定性,4次循环使用后,4-氯苯酚去除率仍可达到73.80%。  相似文献   

3.
为探讨花岗岩母质红壤吸附水中砷(Ⅴ)的效果和机理, 采用静态吸附实验, 研究溶液砷初始浓度、反应时间、温度、pH值等因素对红壤吸附水中砷的影响.当溶液砷初始浓度小于5.0 mg/L时, 红壤对砷的去除率均大于97%;随着砷初始浓度增大, 去除率逐渐降低; 反应初期(0~120 min), 红壤对砷的去除率迅速增大至95.0%左右.此后, 去除率缓慢增大, 直到720 min后, 去除率达到97.0%左右, 并趋于稳定; 在砷初始浓度一定时, 红壤对砷的吸附量随着温度的升高逐渐增加, 但增加幅度较小; 红壤对砷的去除率随着体系pH值的增大呈减小趋势; 正交试验表明, 在砷初始浓度为5.0 mg·L-1、反应时间为120 min、pH为5.0及反应温度为40℃的组合下, 红壤对砷的去除率最大.   相似文献   

4.
常影  姜宁  雷抗  孙艳丰  周睿 《世界地质》2014,33(3):702-707
零价铁和硝基苯反应后生成二价铁和苯胺,而苯胺也是地下水污染物。硫酸根自由基具有强氧化性,可以降解苯胺。而二价铁可以活化过硫酸盐产生硫酸根自由基,进而去除苯胺。本文研究了二价铁浓度、过硫酸盐浓度、苯胺初始浓度、体系初始pH、反应温度等因素对二价铁活化过硫酸盐去除水中苯胺处理效率的影响。结果表明:1)Fe2+活化过硫酸盐生成SO-4·能快速并有效氧化降解苯胺,对于目标浓度为1 000 mg/L的苯胺而言,Fe2+浓度为3.3 mmol/L,Na2S2O8浓度为4.4 mmol/L时,对苯胺有较佳降解效果,苯胺的降解率为86.33%。2体系对较低浓度的苯胺降解效果较好,当污染物初始浓度由1 000 mg/L降低到500 mg/L和100 mg/L时,苯胺降解率由86.33%升高为90.27%和97.16%。3初始pH对苯胺的降解率影响较大,中性条件下(pH=7左右)降解率较好,高初始pH(pH=9,11)和低初始pH条件(pH=3,5)下均低于中性条件下苯胺的降解效率。4体系的温度变化对降解率影响不明显。  相似文献   

5.
为实现水环境中微囊藻毒素的高性能检测,利用农业废弃物合成了具导电性能的生物炭颗粒,并将其作为导电材料构建了对微囊藻毒素-LR具电化学免疫检测性能的生物模板电极。实验结果表明：该电极具有很好的电催化性能,在电解液中,能够在短时间（5 min）内有效识别微囊藻毒素-LR的存在;利用差分脉冲伏安法检测发现在0.0~5.0 nmol/L的检测范围内毒素浓度与响应电流值呈线性递减关系,且最低检测浓度为0.2 nmol/L。该电极对各类不相关分子及离子具有抗干扰能力,表明了该方法可应用于对微囊藻毒素-LR污染的快速、特异性检测。  相似文献   

6.
2011年我国实施了新的生活饮用水卫生标准,卫生指标扩展至106项,并配套了相关的检测方法,其中微囊藻毒素、莠去津采用液相色谱紫外检测器的检测方法;丙烯酰胺、灭草松、2,4-D采用气相色谱-电子捕获检测器的检测方法;呋喃丹、草甘膦采用液相色谱荧光检测器的检测方法。这些检测方法均有前处理程序繁琐、工作量大、可操作性差的缺点,在实际工作中应用较为困难。本文采用超高效液相色谱-串联质谱技术（UPLC-MS/MS）,建立了水样过0.22 μm滤膜,直接进样测定自来水、地下水及地表水中8种有机污染物（草甘膦、呋喃丹、灭草松、莠去津、2,4-滴、丙烯酰胺、微囊藻毒素-RR和微囊藻毒素-LR）的分析方法。8种化合物在各自的线性范围内线性关系良好,相关系数均不低于0.993,定量下限为0.07~5 μg/L,低、中、高三个加标水平的回收率为94.2%~103.7%,相对标准偏差为1.1%~7.8%。本文建立的方法操作简便,可以实现在6 min内一次性分析8种目标化合物,与国家标准方法相比,显著提高了分析效率;与文献报道的均是单一类化合物检测方法相比,本检测方法具有相似的灵敏度和检测限,但是目标化合物覆盖更全面,分析时间更短。  相似文献   

7.
以Pt为阳极,以Ti纳米管为基底修饰一薄层Pd和Cu构成的多金属纳米电极为阴极,搭建电化学反应器进行去除硝酸盐氮(NO3- N)研究,观察了在不同电流密度、初始浓度和pH值条件下该多金属纳米电极对NO3- N去除率的影响。结果表明,在电流密度为30 mA/cm2,添加050 g/L的 Na2SO4作为支持电解质的条件下,电解90 min后Cu Pd TiO2多金属纳米电极对硝酸盐的去除率可达81%,而相同条件下金属Ti做阴极时对硝酸盐的去除率仅为245%。溶液pH值的改变对 NO3- N的去除效果几乎没有影响;随着电流密度的增高,NO3- N的去除效率也随之提高;而随着溶液初始浓度的升高,NO3- N的去除率反而略有下降。  相似文献   

8.
高岭土吸附剂去除含锰废水中锰离子的实验研究   总被引：13，自引：2，他引：11  
高岭土吸附剂处理含锰废水中锰离子的实验表明:高岭土的最佳粒度为0.177 mm,pH值控制在7.5～ 8.5间,常温搅拌30 min,吸附剂与水量比为12 g∶1 L,对锰离子质量浓度为100 mg/L的废水的处理效果最好,使锰离子质量浓度由100 mg/L降至0.1 mg/L,锰离子的去除率超过90%,达到GB8978-1996工业废水排放的一级标准.高岭土对锰离子吸附的等温吸附曲线符合Freundlich模型,其吸附机理主要是吸附作用和沉淀作用.  相似文献   

9.
已知在无氧条件下天然矿物菱铁矿能成功水解微囊藻毒素-LR(MC-LR),然而实际应用过程中难以避免水中溶解氧(O2)的存在,因此有必要深入研究不同溶氧量(DOC)条件下菱铁矿对MC-LR降解的影响。本文通过在无氧和有氧条件下菱铁矿对MC-LR的降解实验,发现在有氧条件下(溶氧量1.62～21.87 mg/L), MC-LR的降解速率均比无氧条件(k0=0.030 16 mg·L-1·h-1)高且其降解速率随O2含量增加而依次增加,当O2加入量为1.0 mL(溶氧量21.87 mg/L)时,菱铁矿对MC-LR降解速率最大(0.083 34 mg·L-1·h-1),为无氧条件下的2.76倍。通过外加腐殖酸(humic acid, HA)和自由基进行捕获实验,发现FeCO3能直接活化O2产生超氧自由基(·O~-2),以实现对MC-LR的氧化,但外加HA抑...  相似文献   

10.
以亚甲基蓝溶液为模型污染物,在超声波芬顿法协同作用下对亚甲基蓝染料废水的降解作用进行了研究,考察了反应时间、H2O2用量、溶液pH值、Fe^2＋的浓度等因素对亚甲基蓝溶液降解的影响。结果表明,超声波单独降解亚甲基蓝溶液脱色效果不明显,超声波协同H2O2降解亚甲基蓝,加入30%H2O26mL,脱色率约45.80%;溶液pH2.80,Fe^2＋浓度为30mmol/L时,超声波芬顿法协同降解甲基蓝180min,脱色率达92.70%。试验证明,超声波芬顿法是一种降解亚甲基蓝的有效方法。  相似文献   

11.
纳米铁去除饮用水中As(Ⅲ)和As(Ⅴ)   总被引：3，自引：1，他引：2  
黄园英  秦臻  刘菲 《岩矿测试》2009,28(6):529-534
在好氧水体中,As(Ⅲ)比As(Ⅴ)更易迁移,而且在水处理过程中去除效率更低。在实验室合成制得BET比表面积为49.16 m2/g,直径范围为20~40 nm的纳米铁。通过批试验考察纳米铁对As(Ⅲ)和As(Ⅴ)去除能力及其反应动力学情况。结果表明,在pH为7,温度20℃时纳米铁能够快速地去除As(Ⅲ)和As(Ⅴ),在60 m in内,0.25 g纳米铁对起始浓度为968.6μg/L As(Ⅲ)和828.9μg/L As(Ⅴ)的去除率大于99.5%。反应遵循准一级反应动力学方程,标准化后的As(Ⅲ)和As(Ⅴ)比表面积速率常数kSA分别为1.30 mL/(m2.m in)和1.64 mL/(m2.m in)。由实验结果可知,具有高反应活性的纳米铁是用于含砷饮用水处理非常有效的吸附材料。  相似文献   

12.
The main objective of this study is to investigate the possibility of powdered eggshell used as an adsorbent material for removal of humic acid from peat water. The influences of contact time, dose of eggshells, pH, and temperature were the factors considered in the removal processes of humic acid from peat water. In addition, adsorption isotherms of humic acid onto the powdered eggshell were also evaluated with the Langmuir and Freundlich approximations. Our results showed that the equilibrium of the process was eventually established after 60 min of the contact time, and also found that using 5 g of the powdered eggshell nearly 95 % of humic acid has been successfully removed from the peat water. The removal of humic acid gave better result when it was conducted at low pH, and it was almost unaffected the temperatures variation. The data was well fitted to Freundlich isotherm with the correlation coefficient of not <0.999, and could uptake the humic acid about 126.58 mg/g at pH 4.01, estimated from the Langmuir model. The kinetic experimental data proportionally correlated with the pseudo-second-order kinetic model with a rate constant in the range of 0.016–0.112 g mg?1 min?1, while intra-particle-diffusion were the main rate determining step in the humic acid removal process. The powdered eggshell investigated in this study, thus, exhibited as a high potential adsorbent for the removal of humic acid from peat water.  相似文献   

13.
The objective of this study was to explore the extent of 2,4,6-trinitrotoluene synthetic solution and red water mineralization by comparing conventional direct ozonation and multi-stage ozonation-biological treatment process. The alkaline hydrolysis was used for remediation 2, 4, 6-trinitrotoluene and red water at pH = 10.9. Nevertheless, the hydroxyl radicals would be generated by ozone decomposition with ozone dose of 0.177 g/L. The samples were subjected to chemical oxygen demand and total organic carbon analysis to monitor pollutants removal. The rate of 2, 4, 6-trinitrotoluene and red water pollutants degradation were quantified using high performance liquid chromatography. 2, 4, 6-trinitrotoluene synthetic solution resulted 55.5 % chemical oxygen demand removal by 3 h direct ozonation. Following direct ozonation the biological treatment twenty four hours chemical oxygen demand reached 98.9 % and 98.7 % removal using humic acid and river water 1 % ( v/v) inoculation singly and respectively. Conventional direct ozonation showed non significant change in total organic carbon degradation. While on using multi-stage ozone-biological treatment process where humic acid and/or river water were used as inoculums singly and respectively, total organic carbon fulfilled 73 % and 98.3 % removal. The process was one hour direct ozonation and followed by three days multi-stage ozone-biological treatment. In multi-stage ozone-biological treatment process, ozonation was effective to decompose total organic carbon and to produce biodegradable dissolved organic carbon easily removed by ozone oxidation up to 98.3 % in 2,4,6-trinitrotoluene synthetic solution. Pollutants removal achieved 99 % in authentic red water effluent using river inoculation 1 % (v/v) in 5 days. Nuclear Magnetic Resonance and Fourier Transformation Infra Red methods were performed to confirm types of pollutants content in red water.  相似文献   

14.
Insolubilized humic acid (IHA) was prepared in the laboratory by heating approach. Through the comparison between the endothermic peaks, optimal heating temperature was determined to be 330°C. The modified IHA then was characterized by TG-DTA, SEM, FTIR, element analysis, and nitrogen adsorption–desorption isotherms. The removal efficiency of p-nitrophenol from the aqueous solution by adsorption onto solid IHA surfaces was shown to be a function of pH, reaction temperature, and p-nitrophenol concentration. Adsorption equilibrium data satisfactorily fitted the Langmuir adsorption isotherm. Under a certain concentration range, the removal rate of p-nitrophenol at pH 3.5 could reach 24, 29, and 35 mg/g at a temperature of 25, 35, and 45±0.1°C. The results suggest that IHA could play a role as a potential efficient absorbent to remove organic contaminants, e.g., utilized to purify water contaminated by organic compounds.  相似文献   

15.
The mechanisms and reaction pathway of UV photo-assisted Fenton-like degradation of progesterone in water and wastewater were investigated. The reaction followed the pseudo-first-order kinetics for both the dark Fenton-like and UV photo-Fenton-like processes. The reaction kinetics of the UV photo-assisted process improved with the presence of humic acid (HA) in wastewater, due to the formation of Fe(III)-HA complexes which enhanced Fe(II) production by a ligand-to-metal charge transfer. The UV photo-assisted process reduced the amount of ferric required to completely degrade progesterone by 60 % and lowered the activation energy to 42 kJ/mol compared to 104 kJ/mol for the dark Fenton-like process. Complete degradation of progesterone was achieved through a multi-step process involving several intermediate compounds.  相似文献   

16.
Chlorate is one of the disinfection byproducts that are formed when chlorine/chlorine dioxide is used as a primary disinfectant. This study investigated the removal of chlorate by photochemical degradation using an advanced reduction process, which is a treatment method that combines a reducing agent with an activating method to generate reducing radicals. The effectiveness of combinations of reducing agents and three UV light sources having a peak output at 254, 365, and 312 nm were evaluated for chlorate removal. Dithionite irradiated by broad-band UVB lamp having the peak energy at 312 nm showed the highest chlorate removal. In pursuit of finding the optimum advanced reduction process conditions, the environmental process variables including pH, reducing agent dose, and light intensity were investigated. Dithionite/UV-B advanced reduction process was effective in weakly acidic conditions (pH < 5), and chlorate removal occurred in two steps. The first was an initial rapid decrease in chlorate concentration that occurred before initiating UV irradiation and was attributed to reaction with dithionite decomposition products. The second step was a slow decrease during UV irradiation that is caused by radicals produced by photolysis of the products of dithionite decomposition. The major product of chlorate destruction was chloride, with negligible amounts of chlorite produced.  相似文献   

17.
周帆  朱健  张鹏  袁松虎 《地球科学》2017,42(6):1039-1044
羟自由基(·OH)是自然环境中氧化活性最强的物种,对物质转化具有重要影响.前期研究发现地下水接触O2可产生·OH,其中Fe2+氧化起主导作用,但地下水化学组成对Fe2+氧化产生·OH的影响尚不清楚.通过室内模拟实验,探究了地下水中常见组分(Ca2+、Mg2+、腐殖酸(HA)和磷酸根)对Fe2+氧化产生·OH的影响.结果表明,pH 6.5时0.357 mM Fe2+在5 h内氧化完全,产生约1.8 μM的·OH;Ca2+(1~6 mM)、Mg2+(1~4 mM)对Fe2+氧化和·OH产生无明显影响;HA(10~30 mg/L)促进Fe2+氧化和·OH产生,促进效果随pH降低而增强;磷酸根(0.01~0.03 mM)抑制Fe2+氧化,对·OH产生的影响为先抑制后促进.   相似文献   

18.
Humic substances exposed to solar light play the role of photosensitizers in aquatic photochemical processes, generating free radicals during UV and visible light irradiation. During irradiation, high molecular weight structures are destroyed and low molecular weight constituents are formed. Alterations of the humic acids metal binding capacity due to their photochemical alterations occur. The present work reports controlled laboratory experimental results on the binding of copper by a certified purified peat humic acid (PPHA) before and after irradiation in a laboratory scale photoreactor. A reference curve of copper binding by photochemically unaltered humic acid was experimentally determined as a function of solution pH by potentiometric titrations. The experimental data series correspond to a pH range from 3 to 8.5, necessary for the simultaneous consideration of complexation and metal species solubility contribution in the obtained results. From the experimental results, it was apparent that copper is strongly bound by humic acid even at the acidic range of pH where the percentage of copper bound reached 60 and 95% at pH values of 3.5 and 5.5, respectively. During 12 and 20 days of irradiation experiments, humic acid photoalteration was experimentally monitored by a size exclusion chromatography system (HPLC-SEC). From the potentiometric titrations of the irradiated humic acid solutions by a copper selective electrode, it was apparent that the copper binding capacity of photoaltered humic acid solutions was significantly reduced for pH values up to 6.  相似文献   

19.
Chemically enhanced wastewater treatment is attracting substantial interest among the currently employed chemical unit processes in wastewater treatment. Coagulation-flocculation has received considerable attention for yielding high pollutant removal, especially color removal. This investigation presents a novel formulation of coagulation-flocculation for color removal from industrial wastewater and illustrates its efficiency, with aid of measurement of solid sludge content, suspended solid content, percentage of solid recovery, UV absorption in wastewater effluent from two automotive factories. The results show that the novel formulation can remove color content from wastewater efficiently. The treated wastewater had UV absorption close to distillated water and color was removed up to 96% by flocculation / coagulation treatment.  相似文献   

20.
Lipids, fulvic acid, humic acid and kerogen were isolated from a lacustrine sediment in which the organic matter is probably derived predominantly from phytoplankton (Lake Haruna, Japan). An alkaline KMnO4 oxidation study of the organic matter showed that distributions of polymethylene chain lengths in the lipids, humic acid and kerogen fractions are almost the same. The polymethylene chains in the sediment are dominant in the kerogen, lipids and humic acid, their relative abundance estimated by the oxidation being: kerogen (42% of the total amounts of polymethylene chains estimated) > lipids (38%) > humic acid (19%) > fulvic acid (1%). It was concluded that algal lipids may have been incorporated into the kerogen and humic acid fractions after the death of the algae and during, after, their deposition.  相似文献   

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