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Solvent Extraction of Copper Enhanced by Mixing Cavities in Micromixer 微混合器混合腔强化铜的溶剂萃取
IF 0.7 4区 工程技术 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2021-01-01 DOI: 10.15261/SERDJ.28.37
A. Sheik, A. Kulkarni, K. Sanjay
A Y micromixer with a macroscopic mixing cavity at the inlet junction was developed. The effects of the mixing cavity on the improvement of extraction of copper by LIX 84I were investigated. The investigated parameters and their ranges were: overall flow rate: 10 – 200 mL/min; microchannel size: 0.5 – 1 mm and mixing cavity diameter: 5 – 20 mm. Extraction efficiency, volumetric mass transfer coefficient, kinetics and pressure drop were investigated. The extraction efficiency and the volumetric mass transfer coefficient in the cavity micromixer were significantly higher than the Y micromixer. The volumetric mass transfer coefficient ranged between 1 – 93 s -1 , and the pressure drop between 50 – 500 kPa. The residence time required in the micromixers was two orders of magnitude lesser than that of an agitated batch reactor.
研制了一种入口连接处带有宏观混合腔的Y型微混合器。研究了混合腔对LIX 84I萃取铜性能的影响。研究的参数范围为:总流速:10 ~ 200 mL/min;微通道尺寸:0.5 - 1毫米,混合腔直径:5 - 20毫米。考察了萃取效率、体积传质系数、动力学和压降。腔型微混合器的萃取效率和体积传质系数均显著高于Y型微混合器。体积传质系数在1 ~ 93 s -1之间,压降在50 ~ 500 kPa之间。在微混合器中所需的停留时间比搅拌间歇式反应器短两个数量级。
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引用次数: 0
Complexation Studies of Eu(III) by a Novel Soft N and Hard O Donor Combined Ligand Including N,N,N',N'-Tetrakis(2-pyridylmethyl)-1,3-diaminopropane-2-amide Structure: UV-vis Titration, X-ray Crystallography, EXAFS Spectroscopy Analysis 新型软氮硬氧配体(N,N,N′,N′-四akis(2-吡啶基甲基)-1,3-二氨基丙烷-2-酰胺)与Eu(III)的络合研究:紫外-可见滴定、x射线晶体学、EXAFS光谱分析
IF 0.7 4区 工程技术 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2021-01-01 DOI: 10.15261/SERDJ.28.69
Hao Wu, M. Nakase, Yusuke Inaba, M. Harigai, Tohru Kobayashi, T. Yaita, K. Takeshita, Seong Yun Kim
A novel soft N and hard O donor combined ligand including N,N,N’,N’ -tetrakis(2-pyridylmethyl)-1,3-diaminopropane-2-amide structure (TPTNA) was successfully synthesized. Its structure and complexation of Eu 3+ in solid state and methanol solution respectively were investigated by X-ray crystallography, UV-vis titration and EXAFS spectroscopy. As a result, the chemical stoichiometry of Eu 3+ complex with TPTNA was determined to be 1 : 1 by X-ray crystallography. It was found that one amide unit, two pyridine groups from TPTNA coordinated with one Eu 3+ . However, the Eu-O and Eu-N bond lengths obtained from theoretical fitting of the EXAFS data were consistent with the results from X-ray crystallography studies, reflecting retention of the structure in methanol solution.
成功合成了一种新型的N,N,N ',N ' -四akis(2-吡啶基甲基)-1,3-二氨基丙烷-2-酰胺结构(TPTNA)的软O和硬O给体组合配体。采用x射线晶体学、紫外-可见滴定法和EXAFS光谱法分别研究了其在固态和甲醇溶液中的结构和与Eu 3+的络合作用。通过x射线晶体学分析,确定了铕3+配合物与TPTNA的化学化学计量比为1:1。发现TPTNA的1个酰胺单元、2个吡啶基团与1个Eu 3+配位。然而,从EXAFS数据的理论拟合中得到的Eu-O和Eu-N键长与x射线晶体学研究的结果一致,反映了甲醇溶液中结构的保留。
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引用次数: 0
Selective Separation of Trivalent Europium(III) from Americium(III) using N,N′Dimethyl-N,N′-di-2-phenylethyl-diglycol Amide (MPEDGA) Extractant in Ionic Liquid 离子液体中N,N '二甲基-N,N ' -二-2-苯基乙基二甘醇酰胺(MPEDGA)萃取剂选择性分离三价铕(III)和镅(III
IF 0.7 4区 工程技术 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2021-01-01 DOI: 10.15261/SERDJ.28.49
Seongyun Kim, Tadayuki Takahashi, Hao Wu
A diglycolamide based N , N ′ -Dimethyl- N , N ′ -di-2-phenylethyl-diglycol amide (MPEDGA) extractant was synthesized and dissolved into 1-butyl-3-methylimidazolium nonafluorobutanesulfonate ([C 4 mim][NfO]) to prepare the extraction phase. Its separation performance of Am-241 with Eu-152 in nitric acid solution was investigated. The extraction kinetics were fast and could reach equilibrium within 15 min. When [HNO 3 ] = 0.1 M, the maximum SF Eu-152/ Am-241 was obtained as 124. Moreover, with increase in the concentration of HNO 3 , the extraction ability decreased gradually, and SF Eu-152/ Am-241 decreased as 3 when [HNO 3 ] reached 4 M. Back extraction was successfully completed by using 1 M guanidine carbonate with 0.5 M ethylenediaminetetraacetic acid (EDTA) or 1 M guanidine carbonate with 0.5 M diethylenetriaminepentaacetic acid (DTPA), respectively. Slope analysis revealed a 1:3 complex was formed. Effect of temperature further clarified the extraction process was exothermic.
合成了一种基于二乙醇酰胺的N, N ' -二甲基- N, N ' -二-2-苯基乙基二甘醇酰胺(MPEDGA)萃取剂,并将其溶解于1-丁基-3-甲基咪唑非氟丁磺酸盐([c4mim][NfO])中制备萃取相。研究了其在硝酸溶液中Am-241与Eu-152的分离性能。萃取动力学快速,可在15 min内达到平衡。当[hno3] = 0.1 M时,eu152 / Am-241的最大SF为124。随着hno3浓度的增加,萃取能力逐渐降低,当[hno3]浓度达到4 M时,SF Eu-152/ Am-241降低为3,分别用1 M碳酸胍与0.5 M乙二胺四乙酸(EDTA)或1 M碳酸胍与0.5 M二乙三胺五乙酸(DTPA)完成反萃取。坡度分析显示形成了1:3的络合物。温度的影响进一步明确了提取过程是放热的。
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引用次数: 0
Recovery of Neodymium from Waste Permanent Magnets by Hydrometallurgy Using Hollow Fibre Supported Liquid Membranes 湿法冶金中空纤维支撑液膜法回收废永磁体中的钕
IF 0.7 4区 工程技术 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2020-01-01 DOI: 10.15261/serdj.27.69
A. Ni’am, Yi-Hsien Liu, Ya-Fen Wang, Shyh-Wei Chen, G. Chang, S. You
Achmad Chusnun NI’AM1,2, Yi-Hsien LIU1, Ya-Fen WANG1,3, Shyh-Wei CHEN1,4, Gen-Mu CHANG1 and Sheng-Jie YOU1,3* 1 Department of Environmental Engineering, Chung Yuan Christian University, 200 Chung Pei Road, ChungLi 320, Taiwan; 2 Department of Civil Engineering, Chung Yuan Christian University, 200 Chung Pei Road, Chung-Li 320, Taiwan; 3Research and Development Center for Membrane Technology, Chung Yuan Christian University, 493 Xinzhong N. Road, Chung-Li 320 Taiwan; 4 Environmental Protection Administration, Executive Yuan, Taipei 100, Taiwan (Received September 28, 2019; Accepted October 21, 2019)
Achmad Chusnun NI 'AM1,2,刘义贤1,王亚芬1,3,陈世伟1,4,常根木1,游胜杰1,3* 1中原基督教大学环境工程系,台湾中立市中培路200号;2中原基督教大学土木工程系,忠里忠培路200号,台湾忠里320;3中原基督教大学膜技术研究与开发中心,台湾中黎市新中北路493号;4行政院环境保护署,台北市100(2019年9月28日收稿;接受2019年10月21日)
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引用次数: 9
Effect of Diglycolamide Ligands Structure on Extraction Performance of Heavy Rare Earth Ions 二乙醇酰胺配体结构对重稀土离子萃取性能的影响
IF 0.7 4区 工程技术 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2020-01-01 DOI: 10.15261/serdj.27.81
Huihui Du, Xiujing Peng, Yu Cui, Guoxin Sun
The properties of four different extractants, TODGA ( N,N,N',N' -tetraoctyl-diglycolamide), T2EHDGA ( N,N,N',N' -tetraisooctyl-diglycolamide), DPDODGA ( N,N' -dipropyl- N,N' -dioctyl-diglycolamide) and DIPDODGA ( N,N' -diisopropyl- N,N' -dioctyl-diglycolamide), to extract heavy rare earth metal ions in hydrochloric acid were studied to understand the relationship between the chemical structure of the extractant and the extraction properties of rare earth metal ions. The extraction order of heavy rare earths in n -octane: n -octanol = 9:1 diluent was as follows: DIPDODGA > DPDODGA > TODGA > T2EHDGA. Alkyl chain shows great influence on extraction ability and the extractants with short chain can effectively extract heavy rare earth ions even at a concentration of less than 1.0 mol/L. The extraction mechanism was proposed with the results of slope methods, IR (Infrared) spectrometer and DFT (Density Functional Theory) theoretical study. T2EHDGA forms binuclear and the other three extractants form mononuclear extracted species with heavy rare earth ions.
研究了TODGA (N,N,N′,N′-四辛基-二乙醇酰胺)、T2EHDGA (N,N,N′,N′-四异辛基-二乙醇酰胺)、DPDODGA (N,N′-二丙基- N,N′-二辛基-二乙醇酰胺)和DIPDODGA (N,N′-二异丙基- N,N′-二辛基-二乙醇酰胺)四种不同萃取剂在盐酸中萃取重稀土金属离子的性能,了解萃取剂的化学结构与稀土金属离子萃取性能的关系。在正辛烷:正辛醇= 9:1的稀释液中,重稀土的萃取顺序为:dipdga > DPDODGA > TODGA > T2EHDGA。烷基链对萃取能力影响较大,短链萃取剂即使在浓度小于1.0 mol/L时也能有效萃取重稀土离子。利用斜率法、红外光谱法和密度泛函理论对其萃取机理进行了分析。T2EHDGA与重稀土离子形成双核萃取物,其余三种萃取物形成单核萃取物。
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引用次数: 5
Application of Ionic Liquids in Solvent Extraction of Platinum Group Metals 离子液体在溶剂萃取铂族金属中的应用
IF 0.7 4区 工程技术 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2020-01-01 DOI: 10.15261/serdj.27.1
M. L. Firmansyah, Wataru Yoshida, Takafumi Hanada, M. Goto
Mochamad L. FIRMANSYAH1,2, Wataru YOSHIDA2, Takafumi HANADA2 and Masahiro GOTO2,3 * 1Department of Chemistry, Faculty of Science and Technology, Airlangga University, Jl. Dr. Ir. H. Soekarno, Surabaya 60115, Indonesia; 2Department of Applied Chemistry, Graduate School of Engineering; 3Center for Future Chemistry, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan (Received October 23, 2019; Accepted December 9, 2019)
Mochamad L. firmansyah 1,2, Wataru yoshida a2, Takafumi HANADA2, Masahiro goto 2,3 * 1日本国立大学化学与技术学院化学系,吉林大学,Jl。红外博士。苏加诺,泗水60115,印度尼西亚;2工程研究生院应用化学系;3九州大学未来化学研究中心,日本福冈西区元冈744号,819-0395(收于2019年10月23日;接受2019年12月9日)
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引用次数: 11
Analysis of the Partitioning Behavior of Horseradish Peroxidase to Phospholipid and Surfactant Membranes 辣根过氧化物酶对磷脂和表面活性剂膜的分配行为分析
IF 0.7 4区 工程技术 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2020-01-01 DOI: 10.15261/serdj.27.113
Saki Fukuma, T. Shimanouchi, K. Yasuhara, Y. Kimura
The partitioning behavior of horseradish peroxidase (HRP) to phospholipid- and surfactant vesicles has been analyzed. Peripheral binding of the zwitterionic phospholipid vesicle membranes is proposed with insertion into the membrane interior of negatively charged surfactant vesicles, resulting from non-electrostatic interaction. The insertion of HRP is interpreted by considering the interaction between headgroups of phospholipid and between headgroups of surfactant.
研究了辣根过氧化物酶(HRP)对磷脂囊泡和表面活性剂囊泡的分配行为。两性离子磷脂囊泡膜的外周结合是通过插入带负电荷的表面活性剂囊泡的膜内部,这是由非静电相互作用引起的。HRP的插入可以通过磷脂头基之间和表面活性剂头基之间的相互作用来解释。
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引用次数: 2
Removal of Radionuclide Uranium from South China’s Ion-adsorption Rare Earth Leach Liquor Using Solvent Extraction with Naphthenic Acid 环烷酸溶剂萃取法去除华南离子吸附稀土浸出液中的放射性核素铀
IF 0.7 4区 工程技术 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2020-01-01 DOI: 10.15261/serdj.27.39
Zhang Kuifang, Yuping Zeng, Liu Zhiqiang, Cao Hongyang, Zhu Wei, Guo Qiusong
Kuifang ZHANG 1,3,4, Yuping ZENG 2, Zhiqiang LIU 1,3,4*, Hongyang CAO 1,3,4, Wei ZHU 1,3,4 and Qiusong GUO 1,3,4 1Guangdong Research Institute of Rare Metals, Guangzhou 510650, China; 2Department of Radiology, Guangzhou Universal Medical Imaging Diagnostic Center, Guangzhou 510080, China; 3Guangdong Province Key Laboratory of Rare Earth Development and Application, Guangzhou 510650, China; 4State Key Laboratory of Separation and Comprehensive Utilization of Rare Metals, Guangzhou 510650, China (Received January 23, 2019; Accepted April 22, 2019)
张奎芳1,3,4,曾玉平2,刘志强1,3,4*,曹红阳1,3,4,朱伟1,3,4,郭秋松1,3,4 1广东省稀有金属研究院,广东广州510650;2广州市综合医学影像诊断中心放射科,广州510080;3广东省稀土开发与应用重点实验室,广州510650;4稀有金属分离与综合利用国家重点实验室,广东广州510650(收稿日期:2019年1月23日;接受2019年4月22日)
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引用次数: 3
Preliminary Study on Separation of Dy and Nd by Multi-Step Extraction Using TDdDGA TDdDGA多步萃取分离Dy和Nd的初步研究
IF 0.7 4区 工程技术 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2020-01-01 DOI: 10.15261/serdj.27.63
Y. Sasaki, Y. Ban, Keisuke Morita, M. Matsumiya, Ryoma Ono, H. Shiroishi
Mutual separation technique of Dy and Nd in Nd magnets is studied. Dy is more valuable than Nd, and therefore, Dy should be isolated and reused. Lanthanide elements can be extracted thoroughly by using diglycolamide (DGA) extractants, and we use this reagent to recover and isolate Dy. N,N,N’,N’ -Tetradodecyl-DGA (TDdDGA) has a relatively high separation factor (SF) between Dy and Nd (SF: over 10) in the HNO 3 extraction system, so multi-step extraction using TDdDGA is applied to mutually separate them. In the present study, by using the condition, four extraction steps, organic phase: 0.1 M TDdDGA in n -dodecane, aqueous phase: 0.3 M HNO 3 , 92 % Dy can be recovered with 0.7 % co-extraction of Nd.
研究了钕磁体中镝和钕的相互分离技术。Dy比Nd更有价值,因此,Dy应该被分离和重用。二甘醇酰胺(DGA)萃取剂可以彻底地提取镧系元素,我们使用该试剂回收分离了Dy,N,N ',N ' -十四烷基DGA (TDdDGA)在hno3萃取体系中Dy和Nd的分离因子(SF)较高(SF: > 10),因此采用TDdDGA多步萃取将两者相互分离。本研究采用四步萃取条件,即有机相:0.1 M TDdDGA在正十二烷中,水相:0.3 M hno3,共萃取0.7% Nd,可回收92%的Dy。
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引用次数: 5
Effects of Water Molecules on Metal Complexes of Hydroxyoxime and Carboxylic Acid Extractants 水分子对羟基肟和羧酸萃取剂金属配合物的影响
IF 0.7 4区 工程技术 Q4 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2020-01-01 DOI: 10.15261/serdj.27.25
Y. Nishihara, S. Yoshio
Water molecules around the cobalt(II) (Co) and manganese(II) (Mn) complexes of the hydroxyoxime extractant, LIX63 and/or of the carboxylic acid extractant, Versatic acid 10 (VA10), in cyclohexane solvent were investigated using molecular dynamics calculations with simulated annealing. For the complexes of VA10, water molecules were coordinated to the metal ions, and VA10 molecules were found around the complexes. For the complexes of LIX63, a few water molecules were located at ~ 0.4 nm from the metal ions, in addition to the LIX63 molecules were also coordinated to the metal ions. Our trajectory analysis indicates that the water molecules at ~ 0.4 nm are hydrogen-bonded to LIX63 or other water molecules, suggesting that the hydrogen bonding contributes to the stabilization of the metal complex.
采用模拟退火的分子动力学方法研究了环己烷溶剂中羟基肟萃取剂LIX63和羧酸萃取剂Versatic acid 10 (VA10)的钴(II) (Co)和锰(II) (Mn)配合物周围的水分子。对于VA10配合物,水分子与金属离子配位,在配合物周围发现VA10分子。在LIX63配合物中,除了LIX63分子与金属离子配位外,还有少量水分子位于距离金属离子~ 0.4 nm处。我们的轨迹分析表明,~ 0.4 nm处的水分子与LIX63或其他水分子形成了氢键,表明氢键有助于金属配合物的稳定。
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引用次数: 0
期刊
Solvent Extraction Research and Development, Japan
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