JOURNAL OF MOLECULAR LIQUIDS
·
2022
·
IF 6.633
Hongjun Zang,Yimo Feng,Jing Lou,Kai Wang,Changchun Wu,Zhipeng Liu,Xi Zhu
Ionic liquids have shown good catalytic performance and been widely used in the biomass conversion process due to their unique properties, including environmental friendship, low toxicity, and simple preparation. In this work, a series of novel piperidinium-based ionic liquids were synthesized under mild conditions via a simple protonation reaction or nucleophilic substitution reaction. Among them, 4,4′-(propane-1,3-diyl)bis(1-(carboxymethyl)piperidin-1-ium) chloride ([PDCMPi]Cl) displayed the best catalytic performance. The highest yield (42.81 %) of 3A5AF from NAG was obtained after reacting in N-methyl-pyrrolidone (NMP) in the presence of piperidinium-based ionic liquids at 180 °C for 20 min under normal atmospheric conditions. Additionally, ionic liquid [PDCMPi]Cl showed good catalytic activity in six repeated catalytic runs. Meanwhile, a possible reaction pathway was also proposed on the basis of the results of NMR spectra.
研究领域:
催化化学
·
绿色化学
·
生物质能源
·
有机合成
·
离子液体化学
✓ 已验证
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2022
·
IF 5.518
Lei Sun,Meng Yang,Hao Guo,Tingting Zhang,Ning Wu,Mingyue Wang,Fan Yang,Junye Zhang,Wu Yang
Herein, covalent organic framework (COF) and covalent triazine framework (CTF) have been successfully combined for electrochemical sensing via carboxylated multi-walled carbon nanotubes (COOH-MWCNTs). The COF was synthesized from 1,3,5-tris-(4-formylphenyl) benzene (TFPB) and benzidine (BD), named TFPB-BD-COF. Meanwhile, CTF was synthesized by 1, 4-dicyanobenzene (DCB), then chemically activated with KOH at 700 °C to obtained chemically activated porous product, caCTF-1–700. A novel electrochemical sensor based on TFPB-BD-COF/caCTF-1–700/COOH-MWCNT composite was constructed for simultaneous detection of acetaminophen (ACOP) and 4-aminophenol (4-AP). The electrochemical behaviors of the ACOP and 4-AP on the TFPB-BD-COF/caCTF-1–700/COOH-MWCNT electrode were explored via differential pulse voltammetry (DPV) and cyclic voltammetry (CV). The fabricated TFPB-BD-COF/caCTF-1–700/COOH-MWCNT composite modified glassy carbon electrode (GCE) possessed outstanding electrocatalytic performance for the electro-oxidation of acetaminophen (ACOP) and 4- aminophenol (4-AP). Under optimal conditions, the linear ranges were 0.6–150 μM for ACOP and 4-AP, respectively, with the low detection limits of 0.053 μM and 0.075 μM, respectively. In addition, it also showed excellent selectivity, repeatability, reproducibility and stability. The proposed modified electrode was applied for the determination of ACOP and 4-AP in acetaminophen tablet and Yellow river water and obtained satisfactory recovery between 96.31~103.96% and 97.2~101.6%, respectively.
研究领域:
分析化学
·
电化学
·
生物传感器
·
药物分析
·
环境监测
·
材料科学
·
纳米技术
✓ 已验证
DOI
高影响因子
Science China-Materials
·
2021
·Vol. 65
·期 5
·1285-1293
·
IF 8.273
Zheng Mang,Li Qi,Liu Mingyang,Liu Jianan,Zhao Chen,Xiao Xudong,Wang Hongli,Zhou Jing,Zhang Liping,Jiang Baojiang
As an n-type semiconductor, In 2 O 3 is considered a promising photocatalyst for producing amino acids using biomass derivatives as precursors. However, similar to other intrinsic semiconductors, In 2 O 3 suffers from poor charge dynamics. Herein, we show the synthesis of Mo-doped In 2 O 3 (Mo-In 2 O 3 ) with a porous rod-shaped structure through a one-step solvothermal reaction followed by calcination. Under visible-light irradiation, Mo-In 2 O 3 achieves a high conversion rate of 81% for the reaction that transforms lactic acid into alanine with a selectivity of 91%. Spectroscopic techniques and density functional theory calculations reveal that Mo doping introduces defect states slightly below the conduction band of In 2 O 3 , which improves the separation of photogenerated electron-hole pairs. In addition, Mo atoms on the surface form extra adsorption and reaction centers that greatly enhance the reaction rate. This work provides insights into the development of transition metal-doped semiconductor photocatalysts to produce amino acids.
研究领域:
材料科学
·
光催化
·
半导体材料
·
生物基化学品
·
分子催化
·
纳米材料
✓ 已验证
DOI
高影响因子
CHINESE JOURNAL OF CATALYSIS
·
2015
·Vol. 36
·期 2
·204-208
·
IF 1.964
Zhongkui Zhao,Renzhi Li,Yu Li,Guiru Wang
A clean and highly efficient catalytic aerobic reductive ring-cleavage of 3–methylanthra[1,2- c ]isoxazole-6,11-dione to 1-amino-2-acetylanthraquinone was performed using simple organic amines as organocatalysts and water as a green reaction medium. This method provides a new clean transformation of isoxazole-containing compounds to the corresponding ortho -amino ketones . The catalytic performance of various organic amines was carefully screened, and simple organic primary amines were found to be promising practical catalysts with outstanding catalytic performance. Isopropylamine as the organocatalyst gave 97.2% conversion of 3–methylanthra[1,2- c ]isoxazole-6,11-dione, with 97.2% selectivity to 1-amino-2–acetylanthraquinone, in the presence of oxygen only, using 1 equiv. of hydrazine hydrate at room temperature for 3 h. A possible mechanism is also proposed.
研究领域:
有机化学
·
催化化学
·
绿色化学
·
药物化学
·
合成方法学
✓ 已验证
DOI
高影响因子
JOURNAL OF CHEMICAL AND ENGINEERING DATA
·
2018
·
IF 2.196
Li Zhang,Fangxiang Song,Yonggui Wu,Liang Cheng,Jin Qian,Shuai Wang,Qianlin Chen,Yan Li
In this study, the as-prepared spherical mesoporous silica was modified by amino and cyano groups via grafting, and the amino and carboxyl functionalized adsorption materials (MSS@NH2@COOH) were obtained after cyano group hydrolysis. The introduction of amino and carboxyl groups increases the surface active sites of the materials. The materials were characterized by SEM, TEM, XRD, N2 adsorption/desorption, XPS, etc. BET analysis revealed the amino and carboxyl functionalized mesoporous silica maintained their mesostructure nature and its specific surface area was 113 m2·g–1. TG-DTA and FT-IR confirmed effective grafting on the surface of mesoporous silica with functionalized groups. The simulated wastewater of Ni(II) was carried out to test the adsorption properties of the materials, and several influential factors (pH, initial nickel ion concentration, adsorbent dose) were discussed. The saturated adsorption capacity increased clearly from 46.55 mg·g–1 of MSS to 125.57 mg·g–1 of MSS@NH2@COOH. Even recycling three times, the removal rate of Ni(II) ions using MSS@NH2@COOH as an adsorbent could still be over 75%. Adsorption isotherms, kinetics, and thermodynamics of adsorption were taken to clarify the adsorption process. This newly developed adsorbent material does exhibit good reusable performance and effective removal of the heavy metal ions of Ni(II).
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
Journal of Energy Chemistry
·
2022
·
IF 13.599
Jiang Wang,Gangtie Lei,Teng He,Hujun Cao,Ping Chen
One of the major obstacles to the application of potassium-ion batteries in large-scale energy storage is the lack of safe and effective electrolytes. KNH 2 , a new potassium-ion solid electrolyte has been developed in this study. Its ionic conductivity reaches 4.84 × 10 −5 S cm −1 at 150 °C and can reach 3.56 × 10 −4 S cm −1 after mechanochemical treatment. The result from electron paramagnetic resonance (EPR) measurement shows that the increment of ionic conductivity is dependent on the concentration of nitrogen defects in the KNH 2 electrolyte. To the best of our knowledge, this is the first report that adopts inorganic amide as an electrolyte for potassium-ion battery and initiates the search for a new amide-based solid electrolyte for an all-solid-state potassium-ion battery.
研究领域:
材料科学
·
电化学
·
能源存储
·
固态离子学
·
无机化学
✓ 已验证
DOI
高影响因子
APPLIED ORGANOMETALLIC CHEMISTRY
·
2019
·Vol. 33
·期 9
·e5082
·
IF 3.259
Dongmei He,Li Zeng,Guiqing Zhang,Qinggang Li,Wenjuan Guan,Zuoying Cao,Shengxi Wu
A new compound, α-aminophosphonate derivative containing pyridine ring (PPDE), was designed and synthesized as an extractant for the separation of nickel from metal impurities. Over 94.5% of Ni (II) extraction from sulfuric acid solution was achieved by using PPDE with an equilibrium pH of 4.02. Meanwhile, high separation coefficients of 23.8 for Ni to Co, 84.9 for Ni to Mn, 254.1 for Ni to Ca and 696.7 for Ni to Mg, respectively, were obtained. It was noted that PPDE exhibited an excellent regenerability, and the extraction of Ni with the recycled organic phase ranged from 92.5% to 93.9% during six circulations. The extracted nickel complex was determined as [Ni (PPDE) 2 (DNNSA − ) 2 (H 2 O) 4 ], which was supported by the data obtained from Fourier transform-infrared, UV–Vis and electrospray ionization-mass spectrometry spectra.
研究领域:
无机化学
·
湿法冶金
·
分离科学
·
配位化学
·
环境化学
·
资源回收
✓ 已验证
DOI
高影响因子
JOURNAL OF RARE EARTHS
·
2017
·Vol. 36
·期 3
·304-310
·
IF 2.429
Shengting Kuang,Zhifeng Zhang,Yanling Li,Haiqin Wei,Wuping Liao
The extraction and separation of heavy rare earths (REs) using newly synthesized α-aminophosphonic acid extractant 2-ethylhexyl-3-(2-ethylhexylamino)pentan-3-yl phosphonic acid (HEHAPP, H A ) in n-heptane were investigated from chloride medium. The extraction stoichiometries of lanthanum , gadolinium , yttrium and lutetium are determined to be RE A 3 by the slope analysis method. The favorable separation factors of adjacent heavy REs(Ⅲ), i.e. β Y/Ho , β Er/Y , β Tm/Er , β Yb/Tm and β Lu/Yb , are determined to be 1.87, 1.36, 3.21, 3.22 and 1.93, respectively, when extracted from a binary system at proper condition. The loading capacities of H A for Ho, Er, Yb and Lu increase in the order Ho < Er < Yb < Lu with the values being 0.201, 0.205, 0.216 and 0.229 mol/L, respectively. So H A would be a potential extractant for the separation of heavy REs(Ⅲ). Among inorganic acids such as H 2 SO 4 , HNO 3 and HCl, HCl is tested to be the most effective stripping agent.
研究领域:
湿法冶金
·
稀土化学
·
分离科学与技术
·
无机化学
·
萃取化学
✓ 已验证
DOI
高影响因子
BIOINORGANIC CHEMISTRY AND APPLICATIONS
·
2016
·Vol. 2016
·期 1
·3585781
·
IF 1.488
Xincun Zhang,Fan Yue,Hui Li,Yan Huang,Yi Zhang,Hongmei Wen,Jide Wang
We systematically investigated the reversibility, time lapse, and oxygenation-deoxygenation properties of 15 natural α -amino acid–Co(II) complexes through UV-vis spectrophotometer, polarographic oxygen electrode, and DFT calculations, respectively, to explore the relationship between the coordinating structure and reversible oxygenation of α -amino acid–Co(II) complexes. Results revealed that the α -amino acid structure plays a key role in the reversible oxygenation properties of these complexes. The specific configuration of the α -amino acid group affects the electron of Co(II) transfer to the π ⁎ orbit of O 2 ; this phenomenon also favors the reversible formation and dissociation of Co–O 2 bond when O 2 coordinates with Co(II) complexes. Therefore, the co-coordination of amino and carboxyl groups is a determinant of Co complexes to absorb O 2 reversibly. The group adjacent to the α -amino acid unit evidently influences the dioxygen affinity and antioxidation ability of the complexes. The presence of amino (or imino) and hydroxy groups adjacent to the α -amino acid group increases the oxygenation-deoxygenation rate and the number of reversible cycles. Our findings demonstrate a new mechanism to develop reversible oxygenation complexes and to reveal the oxygenation of oxygen carriers.
研究领域:
无机生物化学
·
金属蛋白化学
·
分子生物学
·
配位化学
·
氧化还原生物学
✓ 已验证
DOI
高影响因子
FUEL
·
2022
·
IF 8.035
Yongtao Zhang,Fulin Chen,Yan He,Fei Wang
CO 2 sequestration based on hydrate technology is considered to be the most promising long-term CO 2 sequestration technology. In this study, a method of using initial stirring to activate CO 2 hydrate formation process was proposed in the aim of saving energy and avoiding the problem of stirring shaft stuck, where the stirring only played a role in activating hydrate formation process. Two amino acids, l -Methionine and d -leucine, were chosen as promoters for improving the formation kinetics of CO 2 hydrates, and l -Methionine presents better than d -leucine. When the concentration of l -methionine solution is equal to or greater than 4 mmol/L, even with the initial stirring of 10 rpm within 8 min, T 90 can be shortened to close to or less than 40 min with a high gas consumption of more than 7.3 mmol gas/mL water, where the promoting effect is similar to the condition of continuous stirring of about 100 min, indicating that about 90 % of the energy consumed for mechanical stirring can be saved. Moreover, an interesting phenomenon was observed that CO 2 hydrates firstly nucleated inside the l -methionine solution, and a large number of small hydrate floccules rapidly formed and filled the entire solution under the action of magnetic stirring, which proved the instantaneous excitation effect of stirring on hydrate formation. This work contributes to rethinking the promoting roles of stirring and promoters in CO 2 hydrate formation.
研究领域:
环境科学
·
能源化学
·
物理化学
·
气体水合物
·
碳捕集与封存
✓ 已验证
DOI
高影响因子
Journal of Materials Chemistry A
·
2020
·Vol. 9
·期 7
·3985-3994
·
IF 11.301
Ruidi Wang,Bei-Bei Xu,Jiachen Wang,Xue Lu Wang,Ye-Feng Yao
The relationship between the structural characteristics and photocatalytic reaction mechanisms of graphitic carbon nitride (g-C3N4) still remains unclarified at the molecular level, which severely hinders the further development of this field. The present study addresses this issue by employing an innovative strategy to investigate the relationship between the H-containing structures of g-C3N4 and its water splitting properties. The exchangeable and unexchangeable protons of the H-containing groups of g-C3N4 were differentiated by selective deuteration, providing a way to distinguish the hydrophilic and relatively non-hydrophilic H-containing groups of g-C3N4. A combination of advanced solid-state NMR approaches reveals that amino group defects (CN2(NHx)) on the C–N skeleton of the photocatalyst likely serve as hydrophilic active sites for facilitating the photocatalytic hydrogen evolution reaction. Accordingly, the newly synthesized g-C3N4 sample having a high concentration of CN2(NHx) by design demonstrates an enhanced H2 yield by a factor of 17 compared to that of pure g-C3N4.
研究领域:
材料化学
·
光催化
·
固体核磁共振
·
表面科学
·
能源材料
✓ 已验证
DOI
高影响因子
POLYMER
·
2018
·
IF 3.483
Dongxue Yang,Lingfeng Li,Binling Chen,Shuxian Shi,Jun Nie,Guiping Ma
In order to improve the removal ability of chitosan (CS) to heavy metal ions , in this study, rich amino-functionalized CS electrospun membranes have been prepared. During the efficient synthesis, poly (glycidyl methacrylate) (PGMA) and polyethylenimine (PEI) were sequentially grafted on the surface of CS electrospun membrane. The success of introduction of amino-group on the CS were confirmed by X-ray diffractometer (XRD), attenuated total reflection-fourier transform infrared (ATR-FTIR), and X-ray photoelectron spectroscopy (XPS). The ability of remove heavy metal ions (Cr(VI), Cu(II) and Co(II)) of the as-prepared membrane (CS-PGMA-PEI) was investigated. The adsorption equilibrium of the heavy metal ion solutions was rapidly established in 60 min. Adsorption kinetics analysis reveals that the adsorption process of CS-PGMA-PEI electrospun membrane was dominated by a Pseudo-second-order model. Its adsorption isotherm can be described by the Langmuir model. The maximum adsorption capacities calculated by Langmuir model were 138.96, 69.27 and 68.31 mg g −1 for Cr(VI), Cu(II) and Co(II), respectively. The adsorption ability of CS-PGMA-PEI electrospun membrane toward metal ions was found in an order of Cr(VI) > Cu(II) > Co(II). CS-PGMA-PEI membrane also exhibited a good reproducibility and stability. Our study may provide a way to synthesize membranes for water purification .
研究领域:
材料科学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）