共查询到19条相似文献,搜索用时 296 毫秒
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以芦苇秸秆生物炭为基体,制备了磁性水滑石/生物炭复合材料(Fe3O4-Mg/Al-LDH/BC)。考察不同pH、Fe3O4-Mg/Al-LDH/BC投加量、初始磷浓度、吸附时间以及反应温度对Fe3O4-Mg/Al-LDH/BC吸附磷的影响。结果表明:Fe3O4-Mg/AlLDH/BC对磷的吸附符合准二级动力学模型和Freundlich模型,吸附过程是自发的吸热反应。在最佳的实验条件下(Fe3O4-Mg/Al-LDH/BC投加量为5.0g/L,磷初始质量浓度为20 mg/L,pH为6.0,温度为30℃,吸附时间为120 min),Fe3O4-Mg/AlLDH/BC对磷的去除率可达99.24%,该材料是一种新型高效的磷吸附材料。 相似文献
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利用化学沉淀法制备磁性四氧化三铁/石墨烯(Fe3O4/GE)纳米复合材料,并将其与H2O2构成非均相Fenton体系用于催化降解水中微量的17β-雌二醇(E2),研究了初始p H值,初始H2O2浓度,催化剂用量对E2降解的影响。结果表明,Fe3O4/GE纳米复合材料在无需外加光源的条件下能够有效催化降解E2。在p H 7.0,E2初始浓度为1 mg/L,初始H2O2浓度为15 mmol/L,Fe3O4/GE投加量为15 mg/L的条件下,反应8 h后可去除92.9%的E2。Fe3O4/GE具有便捷的磁分离特性和稳定的催化活性,经过7次循环使用后对E2的降解效率仍保持在91.5%左右。 相似文献
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采用水相共沉淀法制备小尺寸磁性Fe3O4纳米颗粒,以没食子酸作为还原剂和表面修饰剂,还原Ag[(NH3)2]’制备出Fe3O4/Ag磁性纳米颗粒。研究该磁性纳米颗粒对水溶液中铅离子的吸附行为,研究结果表明,pH为7.0,吸附温度30℃时可得到最好的处理效果,铅的去除率可达99.7%以上,Fe3O4/Ag颗粒吸附行为符合二级动力学模型(R2〉0.99)。该磁性纳米颗粒经过多次再生处理后,仍具有很好的吸附效果,表明Fe3O4/Ag在水处理方面拥有良好的应用前景。 相似文献
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采用共沉淀法制备了纳米Fe3O4磁性粒子。应用透射电子显微镜(TEM)、扫描电子显微镜(SEM)、X-射线衍射仪(XRD)和振动样品磁强计(VSM)等对纳米磁性粒子的粒径、结构、形貌、磁性能进行了表征,进行了磁分离沉降性能和腐殖酸吸附去除实验研究。结果表明:在未添加任何分散剂的条件下,制得的纳米Fe3O4磁性粒子主要呈球状,平均粒径约11nm,为典型的反尖晶石结构;饱和磁化强度、矫顽力和剩余磁化强度分别为73.10emu/g、159.2A/m和0.41emu/g;磁分离沉降速度为重力场的50倍;纳米Fe3O4磁性粒子对腐殖酸的吸附符合Langmuir型吸附等温线。 相似文献
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采用溶剂热法成功制备了具有新型形貌的Fe3O4/CS单分散磁性纳米绒球。选取Fe3O4/CS纳米绒球作为磁性吸附剂,研究了其脱除水中五氯酚钠(PCP-Na)的吸附性能。吸附平衡实验表明,Fe3O4/CS吸附脱除PCP-Na的吸附过程能在30 min以内迅速实现吸附平衡,且对于初始浓度为100 mg/L、初始pH为6.5的PCP-Na溶液,在25℃吸附条件下能使溶液中的PCP-Na去除率高达91.5%。吸附等温线和吸附动力学研究表明,Fe3O4/CS吸附脱除PCP-Na的吸附过程属于放热反应,遵循Langmuir吸附模型,符合Lagergren二级动力学方程。此外,在完成吸附过程后,通过一块永久磁铁即能从吸附溶剂中迅速分离出Fe3O4/CS,从而实现吸附剂的有效分离和重复利用,显示了该磁性吸附剂的优越性和用于实际废水处理的潜力。 相似文献
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《环境工程学报》2016,(5)
在模拟原沉积物弱碱性及含水率的条件下,分别研究了2种高级氧化反应体系:H_2O_2辅助加入催化剂Fe SO4或Fe2(SO4)3及Na2S2O8辅助加入催化剂Fe SO4或Ca O及热催化对污染滩涂沉积物中石油烃的去除效果及其影响因素。同时,还模拟研究了长江口潮汐作用对滩涂石油污染修复效果的影响。研究表明:H_2O_2与样品的质量投加比为0.05,FeSO4和Fe2(SO4)3与H_2O_2摩尔投加比均为0.1时,石油烃去除率分别达到48.9%和57.4%;Na2S2O8本身氧化能力较强,单一Na2S2O8与样品的质量比大于0.01时,石油烃去除率达到46%以上;而在Na2S2O8最佳投加比条件下,Fe SO4、Ca O与Na2S2O8摩尔比为0.05和0.9时,去除率分别达到60.4%和51.3%以上,同时最佳催化温度为50℃。潮汐作用对芬顿试剂氧化修复滩涂石油污染具有促进作用,而高浓度污染滩涂区域建议采用阻隔修复。 相似文献
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Highly stable Fe-Pd bimetallic nanoparticles were prepared with 0.2% (w/w) of sodium carboxylmethylcellulose (CMC) as a stabilizer. The effectiveness of the stabilized Fe-Pd nanoparticles was studied for degradation of two chlorinated pesticides (lindane and atrazine) under aerobic and anaerobic conditions. Batch kinetic tests showed that under anaerobic condition the nanoparticles can serve as strong electron donors and completely reduce 1 mgl(-1) of lindane at an iron dose of 0.5 gl(-1) or 1mg l(-1) of atrazine with 0.05 gl(-1) iron with a trace amount (0.05-0.8% of Fe) of Pd as a catalyst. In contrast, under aerobic condition, the nanoparticles can facilitate Fenton-like reactions, which lead to oxidation of 65% of lindane under otherwise identical conditions. Under aerobic condition, the presence of CMC reduced the level of hydroxyl radicals generated from the nanoparticels by nearly 50%, and thus, inhibited the oxidation of the contaminants. While the particle stabilization greatly enhanced the anaerobic degradation, it did not appear to be beneficial under aerobic condition. The degradation rate was progressively enhanced as the Pd content increased from 0.05% to 0.8% of Fe, and the catalytic effect of Pd was more significant under anaerobic condition. Under anaerobic condition, lindane is degraded via dihaloelimination and dehydrohalogenation, whereas atrazine is by reductive dechlorination followed by subsequent reductive dealkylation. Under aerobic condition, reactive oxygen species and hydroxyl radicals from the iron nanoparticles are responsible for oxidizing the pesticides. Lindane is oxidized via dechlorination/dehydrohalogenation, whereas atrazine is destroyed through dealkylation of the alkylamino side chain. 相似文献
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1-2-7-三氨基-8-羟基-3-6-萘二磺酸(TAHNDS)作为偶氮染料的脱色产物很难被常规的厌氧-好氧染料废水处理工艺所去除。研究了未经驯化的活性污泥对TAHNDS的缺氧转化效果。结果表明,只有在特定的缺氧条件下(ORP在-50~-150 mV之间),TAHNDS才能被活性污泥所降解转化。当浓度在10~80 mg/L范围内,TAHNDS可在72 h内转化93%以上。加入100 mg/L的硝酸盐和0.64 mmol/L的氧化还原介体蒽醌-2-磺酸钠(AQS)可将40 mg/L的TAHNDS的转化时间从84 h缩短到36 h。光谱及HPLC-MS分析表明,TAHNDS在缺氧条件下主要是通过脱氨基和脱磺酸作用生成已知可好氧生物降解的3,5-二氨基-4-羟基萘-2-磺酸。因此,缺氧处理有望作为预处理工艺促进废水中TAHNDS的完全降解。 相似文献
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1—2-7-三氨基-8-羟基-3—6-萘二磺酸(TAHNDS)作为偶氮染料的脱色产物很难被常规的厌氧-好氧染料废水处理工艺所去除。研究了未经驯化的活性污泥对TAHNDS的缺氧转化效果。结果表明,只有在特定的缺氧条件下(ORP在-50~-150mV之间),TAHNDS才能被活性污泥所降解转化。当浓度在10—80mg/L范围内,TAHNDS可在72h内转化93%以上。加入100mg/L的硝酸盐和0.64mmol/L的氧化还原介体蒽醌-2-磺酸钠(AQS)可将40mg/L的TAHNDS的转化时间从84h缩短到36h。光谱及HPLC—MS分析表明,TAHNDS在缺氧条件下主要是通过脱氨基和脱磺酸作用生成已知可好氧生物降解的3,5-二氨基4-羟基萘-2-磺酸。因此,缺氧处理有望作为预处理工艺促进废水中TAHNDS的完全降解。 相似文献
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通过采用ACE装置与烟气NOx分析仪器联用的实验室评价方法,可在更接近实际催化裂化反应-再生过程的条件下,评价助剂对再生烟气中NOx的催化转化性能,同时还可考察助剂的加入对催化裂化产品分布的影响。采用该方法对几种降NOx助剂的性能进行了评价,结果表明,在催化剂体系中含有Pt基CO助燃剂的情况下,加入4%的RDNO;助剂后,烟气NOx降低幅度约30%~40%,且催化裂化产品分布基本不受影响。 相似文献
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纳米Fe_3O_4磁性粒子的制备及吸附性能研究 总被引:1,自引:1,他引:0
采用共沉淀法制备了纳米Fe3O4磁性粒子。应用透射电子显微镜(TEM)、扫描电子显微镜(SEM)、X-射线衍射仪(XRD)和振动样品磁强计(VSM)等对纳米磁性粒子的粒径、结构、形貌、磁性能进行了表征,进行了磁分离沉降性能和腐殖酸吸附去除实验研究。结果表明:在未添加任何分散剂的条件下,制得的纳米Fe3O4磁性粒子主要呈球状,平均粒径约11 nm,为典型的反尖晶石结构;饱和磁化强度、矫顽力和剩余磁化强度分别为73.10 emu/g、159.2 A/m和0.41 emu/g;磁分离沉降速度为重力场的50倍;纳米Fe3O4磁性粒子对腐殖酸的吸附符合Langmuir型吸附等温线。 相似文献
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G. Mamba X. Y. Mbianda A. K. Mishra 《Environmental science and pollution research international》2014,21(8):5597-5609
Gadolinium oxide nanoparticles of diameters <5 nm were uniformly decorated on the surfaces of multiwalled carbon nanotubes which were subsequently used as templates to fabricate gadolinium oxide nanoparticle-decorated multiwalled carbon nanotube/titania nanocomposites. The prepared nanocomposites were evaluated for the photocatalytic degradation of methylene blue under simulated solar light irradiation. Higher photocatalytic activity was observed for the gadolinium oxide-decorated multiwalled carbon nanotube-based nanocomposites compared to the neat multiwalled carbon nanotube/titania nanocomposite and commercial titania. This improvement in photocatalytic activity was ascribed to the gadolinium oxide nanoparticles supported at the interface of the carbon nanotubes and titania resulting in efficient electron transfer between the two components of the composite. Total organic carbon (TOC) analysis revealed a higher degree of complete mineralisation of methylene blue (80.0 % TOC removal) which minimise the possible formation of toxic by-products. The photocatalyst could be re-used for five times, reaching a maximum degradation efficiency of 85.9 % after the five cycles. The proposed photocatalytic degradation mechanism is outlined herein. 相似文献
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Kanniah Paulkumar Balakrishnan Subburathinam Subramanian Elaiya Raja Sudalaimani Dinesh Kumar Radhamani Jila Sivasubramaniam Sudhakar 《Environmental science and pollution research international》2023,30(10):25239-25255
Environmental Science and Pollution Research - Recently, the production of silver nanoparticles and their commercial products has generated increased concern and caused a hazardous impact on the... 相似文献