排序方式: 共有198条查询结果,搜索用时 171 毫秒
121.
采用溶剂热法制备了UiO-66和UiO-66/氧化石墨烯复合材料;以水中四氯化碳为处理对象,研究了吸附时间、污染物浓度及温度等因素对吸附过程的影响,并对吸附过程进行动力学和热力学模拟探讨。结果表明,当四氯化碳浓度为10 mg·L-1、30 ℃时,吸附反应在6 h达到平衡,四氯化碳的去除率为87.5%。UiO-66/氧化石墨烯材料对四氯化碳的吸附过程符合拟二级动力学模型。热力学结果显示ΔG0、ΔS>0,由此判断吸附过程是自发、吸热和熵增加的过程。UiO-66/氧化石墨烯材料中比表面积、表面分散力和晶体缺陷的增加使其对四氯化碳具有更好的吸附性能。 相似文献
122.
采用水热法制备了以氧化还原石墨烯(rGO)为载体的锰钴水滑石(LDH),即MnCo-LDH/rGO复合材料并研究其氧还原性能.在Mn/Co物质的量比为1:3的条件下,MnCo-LDH和MnCo-LDH/rGO的形貌和催化性能最为突出.与MnCo-LDH相比,MnCo-LDH/rGO在Na2SO4溶液中的氧化还原峰更加明显(-0.425V),且峰电流更大,达到0.749mA/cm2.将MnCo-LDH/rGO作为阴极,在120min内持续提供30mA/cm2的电流可使浓度为20mg/L的罗丹明B染料(RhB)降解98.6%,具备良好的降解性能.旋转圆盘(RDE)及自由基淬灭实验结果显示,反应中转移电子数为2,且主要自由基为·OH. 相似文献
123.
为了提高Ti/PbO2电极的稳定性与催化氧化能力,将化学还原氧化石墨烯(RGO)以共沉积的方法修饰于β-PbO2层.通过扫描电镜(SEM),X射线衍射仪(XRD),循环伏安法(CV),电化学交流阻抗(EIS),产羟基自由基(·OH)能力,强化寿命等测试方法对电极性能进行表征,并以酸性红G(ARG)为目标降解物,评估PbO2-RGO电极的催化效果.结果表明,电极经RGO改性后晶型仍为β-PbO2,析氧过电位由1.60V升至1.83V,膜阻抗由144 Ω/cm2降至16.2 Ω/cm2,强化寿命提升了43.6%.通过ARG降解实验表明,改性后的PbO2-RGO电极催化性能均有所提高,其中PbO2-RGO(0.05)电极具有最优的催化能力,120min内对ARG的脱色率可达到98.5%,同时对COD的去除率可达76.89%. 相似文献
124.
氧化石墨烯强化厌氧氨氧化菌的脱氮性能 总被引:1,自引:0,他引:1
采用氧化石墨烯(GO)增强厌氧氨氧化菌的脱氮性能.通过批次试验观察GO对厌氧氨氧化菌的影响,结果表明:当GO浓度为0.15g/L时,厌氧氨氧化菌脱氮性能最好,总氮去除率比无GO的空白组提高18.6%;当GO剂量达到0.2g/L时,厌氧氨氧化菌活性受到抑制,总氮去除率比空白组降低了26.0%.通过对照实验研究GO对厌氧氨氧化菌脱氮性能的长期影响,结果表明:添加GO的R2反应器在每个基质浓度阶段的平均总氮去除率分别为85.3%,83.2%,81.1%,80.8%,均高于未添加GO的R1反应器.对R2反应器周期内脱氮性能进行动力学分析发现,修正的Boltzmann模型和修正的Gompertz模型比修正的Logistic模型更适合描述GO作用下周期内基质去除特性,并且通过模型得到了周期内任意t时刻下的出水总氮浓度和总氮去除率预测公式. 相似文献
125.
以嗜热四膜虫(Tetrahymena thermophila)作为受试生物,考察了纳米材料氧化石墨烯(GO)对其细胞生长率、乙酰胆碱酯酶(AchE)和氧化应激酶活性、生物膜损伤及细胞凋亡的影响,以探究GO的毒性效应.结果表明,GO浓度高于32mg/L时显著抑制嗜热四膜虫的细胞增殖(P<0.05),细胞存活率低于50%;在0~64mg/L实验范围内,随GO暴露浓度增加,细胞内活性氧自由基(ROS)和超氧化物歧化酶(SOD)水平呈先升后降的趋势,AchE活性受抑;GO抑制位于线粒体内膜的琥珀酸脱氢酶(SDH)活性,促进细胞质中乳酸脱氢酶(LDH)的释放;64mg/L GO导致四膜虫细胞出现明显凋亡现象.以上结果显示,中低浓度GO(0~8mg/L)暴露下,氧化应激机制对细胞毒性起主要贡献作用;高浓度GO(32和64mg/L)作用下,四膜虫凋亡现象的产生可能是GO抑制其生长作用导致的. 相似文献
126.
将壳聚糖(CTS)、氧化石墨烯(GO)、3-巯基丙基三甲氧基硅烷(MPTMS)交联制得巯基改性壳聚糖-氧化石墨复合材料(SFCG).采用傅里叶变换红外光谱仪、扫描电子显微镜、元素分析仪对改性前后和吸附前后的材料进行表征.研究吸附剂投加量、温度、时间、初始浓度对吸附效果的影响.实验结果表明,SFCG与CTS相比结构发生很大变化,呈现薄层状结构,表面有褶皱.SFCG能够在短时间内选择性高效吸附Ag(I),最大吸附量为578.41 mg·g-1.通过吸附等温线、吸附动力学、吸附热力学的研究发现,其吸附等温线符合Langumir吸附模型,为单层吸附;吸附过程符合准二级动力学模型,以化学吸附为主,同时吸附过程是自发的、放热的.另外,银是一种贵金属,因此,SFCG将在废水处理和回收贵金属等方面均表现出良好的应用前景. 相似文献
127.
Penghua Wang 《环境科学学报(英文版)》2017,29(6):202-213
Ag–AgBr/TiO_2 supported on reduced graphene oxide(Ag–AgBr/TiO_2/RGO) with different mass ratios of grapheme oxide(GO) to TiO_2 were synthesized via a facile solvothermal-photo reduction method. Compared to the single-, two-and three-component nanocomposites,the four-component nanocomposite, Ag–AgBr/TiO_2/RGO-1 with mass ratio of GO to TiO_2at 1%, exhibited a much higher photocatalytic activity for the degradation of penicillin G(PG)under white light-emitting diode(LED-W) irradiation. The PG degradation efficiency increased with the increase of mass ratio of GO to TiO_2 from 0.2% to 1%, then it decreased with the increase of mass ratio of GO to TiO_2 from 1% to 5%. The zeta potentials of RGO-nanocomposites became more negative with the presence of humic acid(HA) due to the negatively charged HA adsorption, resulting in the shift of points of zero charge to lower values of pH. The aggregations of nanocomposites were more significant due to the bridging effect of HA. Furthermore, the aggregated particle sizes were larger for RGO-nanocomposites compared to other nanoparticles, due to the bindings of the carboxylic and phenolic functional groups in HA with the oxygen-containing functional groups in the RGO-nanocomposites.The microfiltration(MF) membrane was effective for the nanocomposites separation. In the continuous flow through submerged membrane photoreactor(sMPR) system, backwashing operation could efficiently reduce membrane fouling and recover TiO_2, and thus indirectly facilitate the PG removal. 相似文献
128.
电化学高级氧化技术是处理有机染料废水的有效技术方法之一,但其应用受传统贵金属电极成本高、易毒化失活等缺陷的限制.本研究采用廉价易得的石墨粉材料,制备氧化石墨烯(GO)催化剂,用于活性黑5(RBk5)染料废水的电催化氧化降解研究.利用透射电子显微镜、X射线光电子能谱、红外光谱、拉曼光谱、循环伏安法和电化学阻抗谱分析材料的结构特性及电化学性能.结果显示,氧化石墨烯具有较高的电子迁移速率,良好的亲水性和电催化活性.不同的RBk5浓度、外加电流、电解质、初始pH值等条件对RBk5的降解效率也有一定程度的影响.其中,电解质因素对材料性能影响最为显著.在RBk5浓度为10mg/L、外加电流为20mA、反应时间为35min、电解质为NaCl的条件下,电催化降解效率可以达到100%. 相似文献
129.
130.
Tian-Feng Li Chen Shen Hua-Xia Zhang Xi-Qing Wang Jiao Jiao Wei Wang 《International Journal of Green Energy》2019,16(3):228-235
In the present work, a novel cellulose-based porous heterogeneous solid acid catalyst encapsulation of ferriferous oxide (Fe3O4) and sulfonated graphene (GO-SO3H) into cellulose to form composite porous microspheres catalyst (GO-SO3H/CM@Fe3O4) was synthesized and evaluated for biodiesel production from Pistacia chinensis seed oil. The SEM, EDS and FTIR analysis revealed that the catalyst GO-SO3H/CM@Fe3O4 owned stronger active sites and GO-SO3H dispersed well in porous surface and inside of cellulose support. Under the optimum conditions, microwave-assisted transesterification process was carried out with the best catalyst amount, i.e. 5 wt% GO-SO3H/CM@Fe3O4 (weight ratio of GO-SO3H/cellulose), and conversion yield reached 94%. The prepared catalyst could be easily separated from reaction solution by extra magnetic field and reclaimed at least five runs. 相似文献