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排序方式: 共有383条查询结果,搜索用时 31 毫秒
1.
采用水热法成功制备了磁性有序介孔碳(Fe-OMC),用于吸附水中双酚A (BPA).采用高倍投射电镜、X射线衍射仪、傅里叶红外光谱仪、比表面积分析仪和振动样品磁强计对Fe-OMC进行表征.结果表明,该吸附剂具备较大的比表面积、独特的有序介孔孔道结构、丰富的含氧官能团以及较强的超顺磁性.Fe-OMC能够高效地吸附去除水中的BPA,平衡吸附量可达72.62mg/g,经过外加磁场分离回收后依旧具备较好的吸附性能.随着BPA浓度从1mg/L提高到20mg/L,其平衡吸附量由8.33mg/g增至91.78mg/g.随着pH值的升高呈现出先降低后升高再降低的趋势,最高吸附量出现在pH=8(75.34mg/g).Fe-OMC对BPA的吸附过程可用准二级吸附动力学模型和Langmuir吸附等温模型进行描述.计算的热力学参数表明,Fe-OMC对BPA的吸附过程是自发进行的放热过程. 相似文献
2.
为解决反冲洗铁锰泥粉末吸附剂(BSPA)使用后难以泥水分离问题,将除铁锰水厂生物滤池产生的反冲洗泥制成颗粒吸附剂(GA)和磁性粉末吸附剂(MPA),并对BSPA、GA和MPA的除砷性能进行了比较,通过SEM、TED、XRD、BET、FTIR等技术对3种材料进行了表征,寻找3种吸附剂之间除砷性能差异的根源.结果表明,BSPA、GA和MPA对As (V)的最大吸附容量分别为40.980,5.048,8.694mg/g,改性后的吸附材料GA和MPA对砷的吸附能力下降.BSPA是一种以纤铁矿为主的无定形结构混合物,并混有针铁矿和结晶度差的水铁矿,GA的XRD图谱中出现石英晶体和少量赤铁矿晶体的衍射峰,而MPA的主要成分为结晶程度较高的磁赤铁矿.3种材料中均存在有利于吸附的含羟基官能团.BSPA、MPA和GA的比表面积分别为253.150,238.660,43.803m2/g.物相改变且结晶程度增加、表面羟基减少和比表面积降低是导致GA和MPA的砷吸附容量比BSPA低的主要因素. 相似文献
3.
Effects of the surface chemistry of macroreticular adsorbents on the adsorption of 1-naphthol/1-naphthylamine mixtures from water 总被引:1,自引:0,他引:1
ZHANG Wei-ming CHEN Jin-long CHEN Qun HE Min-yang PAN Bing-cai ZHANG Quan-xing 《环境科学学报(英文版)》2005,17(5):782-785
The adsorption behaviors of 1-naphthol, 1-naphthylamine and l-naphthol/l-naphthylamine mixtures in water over two macroreticular adsorbents were investigated in single or binary batch systems at 293 K, 303 K and 313 K respectively. All the adsorption isotherms in the studied systems can be adequately fitted by Langmuir model. In the case of aminated macroreticular adsorbent NDA103, 1-naphthol is adsorbed to a larger extent than 1-naphthylamine; while, the opposite trend is found for nonpolar macroreticular adsorbent NDA100. It is noteworthy that at higher temperature(303 K and 313 K), the total uptake amounts of 1-naphthol and 1-naphthylamine in all binary-component systems are obvious larger than the pure uptake amounts in single-component systems, which is presumably due to the cooperative effect primarily arisen from the hydrogen-bonding interaction between the loaded 1-naphthol and 1-naphthylamine molecules. The simultaneous adsorption systems were confirmed to be helpful to the selective adsorption towards 1-naphthol according to the larger selective index. 相似文献
4.
AT-SS复合颗粒吸附剂的制备和除铅性能研究 总被引:6,自引:0,他引:6
通过颗粒吸附剂在含铅溶液中的振荡实验.研究了凹凸棒石粘土(AT)和钢渣(CS)、水泥(SN)、石英砂(SS)制得的多种复合颗粒吸附剂的除铅性能及制备条件.确定出最佳颗粒吸附剂为AT-SS,混合比为5:1,700℃下焙烧120min.对铅的静态吸附容量高达500mg/g以上,动态吸附容量为60mg/g.在1.5ml/min的流速下,穿透时间为20h,洗脱回收率为48.3%.当Pb进样量为200mg/L时,AT-SS吸附剂在236倍床体积之内,流出液浓度低于排放标准. 相似文献
5.
Liu Fuqiang Xia Mingfang Fei Zhenghao Chen Jinlong Li Aimin 《Frontiers of Environmental Science & Engineering in China》2007,1(1):73-78
Both bottle-point and column-feeding experiments involving different solutes and sorbents were carried out to investigate
the adsorption selectivity and separation performance of salicylic acid and 5-sulfosalicylic acid. Their adsorption isotherms
onto such hypercrosslinked polymeric adsorbents as NDA-100 and NDA-99 could be well described by the Freundlich equations
whose characteristics describe extrathermic and favorable adsorption processes. The adsorption towards NDA-100 mainly depended
on the π-π interaction, while that towards NDA-99 was extremely influenced by the static-electric interaction. Additionally,
the adsorptive capacity of salicylic acid on NDA-99 decreased while it increased on NDA-100 with the presence of 5-sulfosalicylic
acid in the adsorptive environment as the competitive component. Comparatively, the adsorption capacity of 5-sulfosalicylic
acid decreased on both resins with salicylic acid as the competitive component. In fact, the difference in the interaction
between adsorbent and adsorbate resulted in the straight antagonism on the effective adsorption sites on the adsorbent. In
conclusion, the adsorption selectivity of salicylic acid onto NDA-100 was obviously larger than that onto NDA-99 with the
existence of 5-sulfosalicylic acid in the adsorptive environment. A satisfactory separation and recovery of tested solutes
in aqueous phase could be foreseeably achieved by the sequencing adsorption technique involving NDA-100 as well as NDA-99.
Translated from Environmental Pollution & Control, 2005, 27(8): 570–574 [译自: 环境污染与防治] 相似文献
6.
CMK-3 and C-FDU-15 samples were synthesized using hard-templating and evaporationinduced self-assembly(EISA) methods,respectively.The pore structures of CMK-3 and CFDU-15 as well as commercial activated carbon were characterized by means of X-ray diffraction,field emission scanning electron microscopy,transmission electron microscopy,and N_2 adsorption–desorption.Adsorption of NO was investigated by means of thermogravimetric analysis,temperature-programmed desorption of NO + O_2,and in situ diffuse reflectance Fourier transform infrared spectroscopy.The results show that the CMK-3 and C-FDU-15 materials possessed ordered and uniform structures.The coadsorption capacity of NO and O_2 decreased in the sequence CMK-3(88.6 mg/g) C-FDU-15(71.7 mg/g) AC(25.3 mg/g).There were two main adsorption species on CMK-3 and CFDU-15:nitrite and nitrate.Nitrite is converted to nitrate easily.However,the adsorption species were more complex on AC,with nitrite being the main species.Moreover,CMK-3 and C-FDU-15 exhibit excellent regeneration efficiency compared with AC.The excellent NO adsorption performance of CMK-3 and C-FDU-15 was associated with their ordered mesoporous structures and high surface areas.The research provides more options for NO adsorption in the future. 相似文献
7.
天然水体中有机物检测方法的选择与优化 总被引:2,自引:0,他引:2
本文选取并优化了一种准确、易行、适合于天然水样中微量有机物的分析技术.天然水样品中有机物通过混合大孔径吸附树脂XAD-2与XAD-7(4:1,V/V)富集并用二氯甲烷洗脱.所有富集的有机物样品中均加入衍生化试剂N,O-双(三甲基硅基)三氟乙酰胺(缩写为BSTFA)硅烷化,最后采用气相色谱-质谱联用仪分析.为了实验的简便,我们的样品为模拟水样(4L添加定量5β-胆烷(挪威Chiron公司)的去离子水). 相似文献
8.
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10.
磷酸微波活化多孔生物质炭对亚甲基蓝的吸附特性 总被引:1,自引:0,他引:1
以甘蔗渣为原料,采用微波辅助H3PO4活化法制备富含含氧酸官能团的中孔生物质炭。通过扫描电子显微镜SEM、傅立叶变换红外光谱FT-IR等技术对生物质炭物理化学性质进行表征,并通过静态实验法,探讨炭样对亚甲基蓝的吸附行为及热力学性质。结果表明,H3PO4活化制备蔗渣生物质炭的适宜条件为浸渍比1:1,烘干时间10h,活化功率900W,活化时间22min,在此条件下制得的生物质炭得率为39.2%,碘值为817mg/g,亚甲基蓝值为229mg/g,为国家一级品标准的1.7倍。红外光谱分析表明,炭样表面以羟基、羰基、羧基等酸性官能团为主。静态吸附实验表明,Freundlich方程与Redlich—Peterson方程能较好地描述等温吸附行为,表现为优惠吸附。热力学研究表明,吸附吉布斯自由能(△G0)〈0,说明吸附反应是自发过程,而吸附标准焓变(△H0)〉70KJ/mol,表明亚甲基蓝在制备炭样上的吸附是吸热反应,升温有利于吸附,且化学反应在吸附过程中发挥了重要作用。 相似文献