WO2019223051A1 - 光催化电极耦合微生物燃料电池促进焦化废水处理方法 - Google Patents
光催化电极耦合微生物燃料电池促进焦化废水处理方法 Download PDFInfo
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- fuel cell
- rgo
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- 238000004939 coking Methods 0.000 title claims abstract description 43
- 230000001699 photocatalysis Effects 0.000 title claims abstract description 37
- 230000000813 microbial effect Effects 0.000 title claims abstract description 29
- 239000000446 fuel Substances 0.000 title claims abstract description 27
- 238000000034 method Methods 0.000 title claims abstract description 12
- 238000004065 wastewater treatment Methods 0.000 title abstract description 5
- 230000001737 promoting effect Effects 0.000 title abstract 2
- 239000002351 wastewater Substances 0.000 claims abstract description 40
- 239000012528 membrane Substances 0.000 claims abstract description 14
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 13
- 229910052721 tungsten Inorganic materials 0.000 claims abstract description 11
- 239000010937 tungsten Substances 0.000 claims abstract description 11
- 239000002131 composite material Substances 0.000 claims abstract description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 5
- 230000003197 catalytic effect Effects 0.000 claims abstract description 5
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims abstract description 5
- 244000005700 microbiome Species 0.000 claims abstract description 4
- 229910001220 stainless steel Inorganic materials 0.000 claims abstract description 3
- 239000010935 stainless steel Substances 0.000 claims abstract description 3
- 210000004027 cell Anatomy 0.000 claims description 18
- 238000006243 chemical reaction Methods 0.000 claims description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 12
- 239000002957 persistent organic pollutant Substances 0.000 claims description 9
- -1 tungsten halogen Chemical class 0.000 claims description 9
- 210000000170 cell membrane Anatomy 0.000 claims description 6
- 230000000593 degrading effect Effects 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 claims description 4
- 239000008367 deionised water Substances 0.000 claims description 4
- 229910021641 deionized water Inorganic materials 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
- 238000003756 stirring Methods 0.000 claims description 4
- 238000005119 centrifugation Methods 0.000 claims description 2
- 238000010276 construction Methods 0.000 claims description 2
- 238000001816 cooling Methods 0.000 claims description 2
- 238000001035 drying Methods 0.000 claims description 2
- 238000000227 grinding Methods 0.000 claims description 2
- 229910052738 indium Inorganic materials 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000003344 environmental pollutant Substances 0.000 claims 1
- 231100000719 pollutant Toxicity 0.000 claims 1
- 229910002915 BiVO4 Inorganic materials 0.000 abstract description 4
- 150000002367 halogens Chemical class 0.000 abstract description 4
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 abstract description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 abstract 1
- 230000015556 catabolic process Effects 0.000 description 15
- 238000006731 degradation reaction Methods 0.000 description 15
- 239000003054 catalyst Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 230000008878 coupling Effects 0.000 description 5
- 238000010168 coupling process Methods 0.000 description 5
- 238000005859 coupling reaction Methods 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 239000011941 photocatalyst Substances 0.000 description 5
- 238000005273 aeration Methods 0.000 description 4
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 3
- 241000270722 Crocodylidae Species 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- RKTYLMNFRDHKIL-UHFFFAOYSA-N copper;5,10,15,20-tetraphenylporphyrin-22,24-diide Chemical compound [Cu+2].C1=CC(C(=C2C=CC([N-]2)=C(C=2C=CC=CC=2)C=2C=CC(N=2)=C(C=2C=CC=CC=2)C2=CC=C3[N-]2)C=2C=CC=CC=2)=NC1=C3C1=CC=CC=C1 RKTYLMNFRDHKIL-UHFFFAOYSA-N 0.000 description 2
- LNNWVNGFPYWNQE-GMIGKAJZSA-N desomorphine Chemical compound C1C2=CC=C(O)C3=C2[C@]24CCN(C)[C@H]1[C@@H]2CCC[C@@H]4O3 LNNWVNGFPYWNQE-GMIGKAJZSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000012028 Fenton's reagent Substances 0.000 description 1
- 101150003085 Pdcl gene Proteins 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000004134 energy conservation Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910021389 graphene Inorganic materials 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000007146 photocatalysis Methods 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000011206 ternary composite Substances 0.000 description 1
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 description 1
- 238000009279 wet oxidation reaction Methods 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F3/00—Biological treatment of water, waste water, or sewage
- C02F3/34—Biological treatment of water, waste water, or sewage characterised by the microorganisms used
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- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/02—Sulfur, selenium or tellurium; Compounds thereof
- B01J27/04—Sulfides
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- C02F1/46—Treatment of water, waste water, or sewage by electrochemical methods
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- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
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- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
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Definitions
- the invention belongs to the technical field of coking wastewater treatment and energy conservation and resource utilization, and relates to the preparation of a La-ZnIn 2 S 4 / RGO / BiVO 4 composite catalyst and a photocatalytic electrode coupled microbial fuel cell assembly, and their synergistic effects.
- HSO 3 - degrades and treats coking wastewater
- HSO 3 - helps to increase the degradation rate of coking wastewater and promotes the treatment of coking wastewater.
- Coking wastewater is mainly produced by the coal industry and the petroleum industry. It is a kind of industrial organic wastewater that is difficult to treat during coking and gas distillation and purification at a high temperature of 960-1000 degrees Celsius. Its composition is very complex and sulfurized. Substances, cyanides, high concentrations of ammonia nitrogen and a large number of heterocyclic polycyclic aromatic hydrocarbon compounds that are difficult to biodegrade. Different treatment methods (physical and chemical methods, biochemical treatment methods, photocatalytic oxidation technology, Fenton reagent method, catalytic wet oxidation technology, etc.) have their own limitations while being able to exert degradation. At present, reports of using La-ZnIn 2 S 4 / RGO / BiVO 4 ternary composite catalysts to degrade coking wastewater in photocatalytic microbial fuel cells have not appeared.
- La-ZnIn 2 S 4 / RGO / BiVO 4 was introduced into the photocatalytic microbial fuel cell reactor to achieve the purpose of degradation.
- La-ZnIn 2 S 4 / RGO / BiVO 4 is used as a catalyst to combine photocatalytic technology with microbial fuel cell technology, which has largely degraded the content of organic pollutants in coking wastewater, and has been used in coking wastewater treatment. There is significant significance in the process.
- RGO reduced graphene oxide
- BiVO4 bismuth vanadate
- the monoclinic scheelite phase has a narrow band gap energy (2.4 eV), and can be used for both ultraviolet and visible light. Produces a response and shows good photocatalytic activity.
- BiVO4 in order to improve the charge separation efficiency and regulate the interaction between BiVO4 and substrate, various metal salts (for example, AgNO3, Cu (NO 3 ) 2 , Ni (NO 3 ) 2 , RuCl 3 , PdCl 2 etc.) Supporting BiVO4 as a cocatalyst can improve its photocatalytic efficiency.
- the RGO electron mediator can be easily extended to semiconductor-based composite photocatalytic systems.
- BiVO 4 treated with RGO shows unique activity in both photocatalytic oxidation of water and degradation of organic pollutants.
- ABXCY type semiconductor ternary sulfide ZnIn 2 S 4 has been widely used in the degradation of dye wastewater, photocatalytic decomposition of water to produce hydrogen, etc. due to its narrow band gap, strong photocatalytic performance, large specific surface area, and good adsorption performance. Widely praised. Heterostructures formed by coupling different catalysts can effectively improve charge separation, and coupling photocatalysis in different absorption wavelength ranges can increase its wavelength absorption range, thereby improving photocatalytic efficiency.
- This application uses La-ZnIn 2 S 4 / RGO / BiVO 4 as an experimental catalyst. It is hoped that this catalyst can effectively degrade the coking wastewater to achieve the effect of adsorbing and degrading organic pollutants in the coking wastewater.
- the invention designs a La-ZnIn 2 S 4 / RGO / BiVO 4 photocatalytic microbial fuel cell assembly, and successfully constructs a photocatalytic electrode coupled microbial fuel cell system.
- the system can not only be used as an electrode, but also have photocatalytic effect and conductivity.
- the overall efficiency of coking wastewater treatment is greatly improved, the energy consumption is lower, and the concentration of organic pollutants in coking wastewater is greatly reduced.
- the system can theoretically degrade coking wastewater, expand the application of supported photocatalysts, and provide some ideas when treating other wastewater.
- the method for photocatalytic electrode coupled with microbial fuel cell to degrade coking wastewater is as follows:
- Photocatalytic electrode coupled microbial fuel cell catalytic treatment system construction The system is divided into two chambers by a proton exchange membrane. One chamber contains microorganisms, and a carbon rod is inserted as a cathode. The other chamber contains coking containing NaHSO 3 Wastewater, the photocatalytic electrode prepared in step (2) is coupled with the microbial fuel cell membrane module as an anode, and a tungsten halogen lamp is placed and connected by a wire to form a circuit. The tungsten halogen lamp irradiates the photocatalytic electrode coupled with the microbial fuel cell membrane module vertically.
- the system integrates the photocatalytic membrane electrode and the microbial fuel cell power generation performance and coupling synergy to adsorb and degrade organic pollutants in coking wastewater; the organic pollutants difficult to degrade in coking wastewater can be effectively adsorbed And degradation, the photocatalyst and microorganisms in the system can well ensure that it does not lose its activity and can continue to generate electricity.
- Figure 1 is a comparison of the effect of degrading coking wastewater under the condition of a photocatalytic electrode and a microbial fuel cell coupling system, with the same concentration of NaHSO 3 and La-ZnIn 2 S 4 / RGO / BiVO 4 catalysts with different RGO contents,
- the abscissa is time (h), and the ordinate is TOC degradation efficiency (%) of coking wastewater.
- Fig. 2 is a comparison diagram of the effect of degrading coking wastewater under the condition of adding the same concentration of NaHSO 3 and Na 2 SO 4 to the anode coking wastewater under the action of a photocatalytic electrode and a microbial fuel cell coupling system.
- the abscissa is time (h)
- the ordinate is (%) the TOC degradation efficiency of coking wastewater.
- Example 1 Different RGO Content of catalyst for degradation of coking wastewater The following are the reasons for this:
- both the membrane module and the halogen lamp are placed in the system, and a carbon rod is placed in the microbial anode separated by a proton exchange membrane, and the photocatalyst is contacted
- the coking wastewater containing NaHSO3 in the system is a photocathode.
- the crocodile clip is connected to the upper part of the membrane.
- the tungsten halogen lamp is placed in the reaction device. The tungsten halogen lamp power is turned off before the reaction.
- Example 2 Degradation of coking wastewater by a system containing NaHSO 3 and Na 2 SO 4 with the same concentration
- both the membrane module and the halogen lamp are placed in the system, and a carbon rod is placed in the microbial anode separated by a proton exchange membrane.
- a carbon rod is placed in the microbial anode separated by a proton exchange membrane.
- One is light.
- the coking wastewater containing NaHSO 3 in the catalyst contact system is a photocathode (the other is the coking wastewater containing Na 2 SO 4 in a photocatalyst contact system is a photocathode, other conditions are the same).
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Abstract
一种光催化电极耦合微生物燃料电池促进焦化废水处理方法,其利用La-ZnIn 2S 4/RGO/BiVO 4和硅溶胶在不锈钢网上固定涂覆的方法形成导电催化复合膜电极,并将膜电极作为阳极,在阳极室内的焦化废水中加入HSO 3
-,阴极室的微生物中插入碳棒,用导线连接,构成电路回路,施加卤钨灯作为光源,作用于催化电极上,构成光催化电极耦合微生物燃料电池处理焦化废水系统。
Description
本发明属于焦化废水处理与节能资源化技术领域,涉及La-ZnIn
2S
4/RGO/BiVO
4复合催化剂及光催化电极耦合微生物燃料电池组件的制备,及其协同作用,并在反应过程中加入HSO
3
- 降解处理焦化废水,HSO
3
-有助于提高焦化废水降解率,为处理焦化废水起到促进作用。
焦化废水主要是由煤工业和石油工业产生的,它是炼焦、煤气在960-1000摄氏度高温干馏、净化过程中,产生的一种较难处理的工业有机废水,其组成成分非常复杂,有硫化物、氰化物、高浓度的氨氮及大量难以生物降解的杂环多环芳香烃化合物等有毒有害物质。不同的处理方法(物理化学法,生化处理法,光催化氧化技术,Fenton试剂法,催化湿式氧化技术等),在能够发挥降解作用的同时都存在着各自的局限性。目前,将La-ZnIn
2S
4/RGO/BiVO
4三元复合催化剂运用到光催化型微生物燃料电池中降解焦化废水的报道还未出现。
为了提高焦化废水降解效果,实验前期将光催化技术和微生物燃料电池相结合,将催化剂La-ZnIn
2S
4/RGO/BiVO
4引入光催化型微生物燃料电池反应器中,以达到降解的目的。目前,以La-ZnIn
2S
4/RGO/BiVO
4作为催化剂,将光催化技术与微生物燃料电池二者技术相结合,很大程度上降解了焦化废水中的有机污染物含量,在焦化废水处理工艺中有重要意义。
目前,用于穿梭光产生电荷的固态电子介体中已被证明有前景的主要有两种材料,贵金属和还原的氧化石墨烯(RGO)。片状RGO材料在特定的层状结构,化学稳定性,提供了优于贵金属的形态多样性和较低的制备成本。
另外,钒酸铋( BiVO
4 ) 因其带隙窄,波长响应范围宽,已被证明是一种具有很好应用前景的光催化剂。BiVO4主要有单斜白钨矿,四方锆石和四方钨白矿3种晶型,其中单斜白钨矿相由于具有较窄的带隙能( 2.4 eV) ,对紫外光和可见光都能产生响应,表现出较好的光催化活性。在以前的研究中,为了提高电荷分离效率和调节BiVO4和底物相互作用,各种金属盐( 例如,AgNO3,Cu(NO
3 )
2,Ni(NO
3 )
2,RuCl
3,PdCl
2等) 作为助催化剂负载在 BiVO4表面可以改善它的光催化效率。而RGO电子介体可以很容易地扩展到基于半导体的复合光催化系统中,用RGO处理的BiVO
4不论在光催氧化分解水还是在有机污染物的降解方面都表现出独特的活性。
而属于 ABXCY 型半导体三元硫化物ZnIn
2S
4,因带隙较窄、光催化性能强、比表面积大、吸附性能好等优点,在降解染料废水、光催化分解水制氢等方面受到了广泛好评。通过耦合不同催化剂形成的异质结构可有效提高电荷分离,将不同吸收波长范围的光催化进行耦合可以增大其波长吸收范围,从而提高光催化效率。
本申请以La-ZnIn
2S
4/RGO/BiVO
4作为实验催化剂,希望以此催化剂能够有效降解焦化废水,以达到吸附和降解焦化废水中有机污染物的效果。
本发明设计了La-ZnIn
2S
4/RGO/BiVO
4光催化型微生物燃料电池组件,成功构建了光催化电极耦合微生物燃料电池系统。该系统不仅可以用作电极,还兼具光催化效果以及导电作用, 整体处理焦化废水的效率大大提高,能耗较低,焦化废水中有机污染物浓度大大降低。该系统理论上可降解焦化废水,扩展了负载型光催化剂的应用,以及在处理其他废水时提供了一些思路。
本发明的技术方案:
光催化电极耦合微生物燃料电池降解焦化废水的方法,步骤如下:
(1)制备La-ZnIn
2S
4/RGO/BiVO
4系列复合物:将 Bi(NO
3)
3·5H
2O溶于14wt% HNO
3中,搅拌,然后向其中加入CTAB溶液,控制CTAB与Bi(NO3)3·5H2O的质量比为1:15;再添加GO,搅拌,得到混合液A液;
将NH
4VO
3溶于2mo/l NaOH溶液中,逐滴加入到A液,控制NH
4VO
3与A液中Bi(NO
3)
3·5H
2O的摩尔比为1:1;用2mol/l NaOH溶液调节pH=6,搅拌;于200℃温度条件下反应2h,冷却,得到混合物;洗涤,离心,烘干,研磨,获得x RGO/BiVO
4,碾磨成粉,即为xRGO/BiVO
4;其中,x为RGO/BiVO
4中RGO与BiVO
4的质量比不大于1.5% ;
将Zn(NO
3)
3·6H
2O、In(NO
3)
3·5H
2O以及过量的TAA溶于去离子水中,再加入La(NO
3)
3和RGO/BiVO
4,加入去离子水,搅拌;于80℃温度条件下反应6h,冷却,得到混合物;经离心,烘干,研磨,获得y La-ZnIn
2S
4/RGO/BiVO
4,碾磨成粉,即为yLa-ZnIn
2S
4/xRGO/BiVO
4;其中,La-ZnIn
2S
4与RGO/BiVO
4的质量比为1:5,y为La与ZnIn
2S
4的质量比0.01;
(2)光催化电极耦合微生物燃料电池膜组件制备:向步骤(1)制备得到的yLa-ZnIn
2S
4/xRGO/BiVO
4系列复合物中添加硅溶胶,yLa-ZnIn
2S
4/xRGO/BiVO
4系列复合物与硅溶胶的比例为1g:1ul,超声均匀,将其涂抹于不锈钢网片上,干燥;
(3)光催化电极耦合微生物燃料电池催化处理系统构建:系统通过质子交换膜分为两室,一室中放有微生物,碳棒插入其中,作为阴极;另一室中为含有NaHSO
3的焦化废水,步骤(2)制备得到的光催化电极耦合微生物燃料电池膜组件作为阳极,并放置卤钨灯,通过导线连接,形成电路,卤钨灯垂直照射光催化电极耦合微生物燃料电池膜组件。
本发明的有益效果:该系统集成了光催化膜电极和微生物燃料电池产电性能以及耦合协同作用,吸附和降解焦化废水中的有机污染物;对焦化废水中难降解的有机污染物能够有效吸附和降解,该系统中的光催化剂和微生物能够很好地保证其不失去活性,并且能够持续产电。
图1是光催化电极与微生物燃料电池耦合系统作用下,加入相同浓度的NaHSO
3,不同RGO含量的La-ZnIn
2S
4/RGO/BiVO
4催化剂条件下,降解焦化废水的效果对比题,图中,横坐标为时间(h),纵坐标为焦化废水的TOC降解效率(%)。
图2 是光催化电极与微生物燃料电池耦合系统作用下,阳极焦化废水中分别加入相同浓度的NaHSO
3和Na
2SO
4处理条件下,降解焦化废水效果对比图。图中,横坐标为时间(h),纵坐标为焦化废水TOC降解效率的(%)。
以下结合技术方案和附图详细叙述本发明的具体实施方式。
实施例一:不同
RGO
含量的催化剂降解焦化废水
在光催化膜电极耦合微生物燃料电池的双室长方体反应器系统中,将膜组件和卤钨灯均放入系统中,用碳棒放入用质子交换膜隔开的微生物阳极中,光催化剂接触系统中的含有NaHSO3的焦化废水为光电阴极,阴极室底部有曝气头持续曝气,用鳄鱼夹连接膜上方,将卤钨灯放入反应装置中,反应前关闭卤钨灯电源,先进行0.5h的暗反应后,再打开卤钨灯电源,光反应4h,反应开始后,前2.5小时每隔0.5h用移液枪进行取样,后两小时每隔1.0h取样,反应共进行4.5h,用TOC/TN检测仪检测样品中TOC含量,并计算焦化废水中有机污染物的降解效果。
图1中,0.5%RGO降解效果最佳,为82.02% 。
实施例二:含有相同浓度的NaHSO
3 和Na
2 SO
4 的体系降解焦化废水
在光催化膜电极耦合微生物燃料电池的双室长方体反应器系统中,将膜组件和卤钨灯均放入系统中,用碳棒放入用质子交换膜隔开的微生物阳极中,一个是光催化剂接触系统中的含有NaHSO
3的焦化废水为光电阴极(另一个是光催化剂接触系统中的含有Na
2SO
4的焦化废水为光电阴极,其他条件相同)阴极室底部有曝气头持续曝气,用鳄鱼夹连接膜上方,将卤钨灯放入反应装置中,反应前关闭卤钨灯电源,先进行0.5h的暗反应后,再打开卤钨灯电源,光反应4h,反应开始后,前2.5小时每隔0.5h用移液枪进行取样,后两小时每隔1.0h取样,反应共进行4.5h,用TOC/TN检测仪检测样品中TOC含量,并计算焦化废水中有机污染物的降解效果。
图2中,含有NaHSO
3的焦化废水和含有Na
2SO
4的焦化废水进行对比,发现含有NaHSO
3的焦化废水光催化膜电极耦合微生物燃料电池的系统中降解焦化废水的效率(82%)远远优于含有Na
2SO
4的焦化废水的降解效率(15%)。
Claims (2)
- 一种光催化电极耦合微生物燃料电池降解焦化废水的方法,其特征在于,步骤如下:(1)制备La-ZnIn 2S 4/RGO/BiVO 4系列复合物:将 Bi(NO 3) 3·5H 2O溶于14wt% HNO 3中,搅拌,然后向其中加入CTAB溶液,控制CTAB与Bi(NO3)3·5H2O的质量比为1:15;再添加GO,搅拌,得到混合液A液;将NH 4VO 3溶于2mo/l NaOH溶液中,逐滴加入到A液,控制NH 4VO 3与A液中Bi(NO 3) 3·5H 2O的摩尔比为1:1;用2mol/l NaOH溶液调节pH=6,搅拌;于200℃温度条件下反应2h,冷却,得到混合物;洗涤,离心,烘干,研磨,获得x RGO/BiVO 4,碾磨成粉,即为xRGO/BiVO 4;其中,x为RGO/BiVO 4中RGO与BiVO 4的质量比不大于1.5% ;将Zn(NO 3) 3·6H 2O、In(NO 3) 3·5H 2O以及过量的TAA溶于去离子水中,再加入La(NO 3) 3和RGO/BiVO 4,加入去离子水,搅拌;于80℃温度条件下反应6h,冷却,得到混合物;经离心,烘干,研磨,获得y La-ZnIn 2S 4/RGO/BiVO 4,碾磨成粉,即为yLa-ZnIn 2S 4/xRGO/BiVO 4;其中,La-ZnIn 2S 4与RGO/BiVO 4的质量比为1:5,y为La与ZnIn 2S 4的质量比0.01;(2)光催化电极耦合微生物燃料电池膜组件制备:向步骤(1)制备得到的yLa-ZnIn 2S 4/xRGO/BiVO 4系列复合物中添加硅溶胶,yLa-ZnIn 2S 4/xRGO/BiVO 4系列复合物与硅溶胶的比例为1g:1ul,超声均匀,将其涂抹于不锈钢网片上,干燥;(3)光催化电极耦合微生物燃料电池催化处理系统构建:系统通过质子交换膜分为两室,一室中放有微生物,碳棒插入其中,作为阴极;另一室中为含有NaHSO 3的焦化废水,步骤(2)制备得到的光催化电极耦合微生物燃料电池膜组件作为阳极,并放置卤钨灯,通过导线连接,形成电路,卤钨灯垂直照射光催化电极耦合微生物燃料电池膜组件。
- 根据权利要求1所述的光催化电极耦合微生物燃料电池降解焦化废水的方法,其特征在于,所述的污染物为焦化废水中的有机污染物。
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CN108793422B (zh) | 2019-09-27 |
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