CHEMICAL ENGINEERING JOURNAL
·
2020
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IF 10.652
Lifeng Chen,Jie Zhang,Xianwen He,Manqing Liu,Qiuyang Wei,Xinpeng Wang,Yuezhou Wei
The measurement of 210 Pb is significant in environmental studies. Lead separation in HCl solution is a vital procedure but suffers from poor efficiency with high labor and time costs. To overcome this problem, a novel anion exchange resin was synthesized and characterized by different techniques followed by studies on the adsorption behaviors towards lead in HCl solution. The results suggest that SiPS-N(CH 3 ) 3 Cl was successfully prepared with small particle size, low water swelling rate, and large specific surface area. The maximum anion exchange capacity resulted from quaternary amine groups was determined to be 1.0 mmol (Cl − )/g. The adsorption activities reached equilibrium within 5 min under selected conditions offering extremely fast adsorption kinetics. The synergistic adsorption mechanism and the competition from co-existing chloride anions were found to be responsible for the lead adsorption performance of SiPS-N(CH 3 ) 3 Cl. Column experiments showed that the feeding volume of lead and HCl had impact on the chemical yield regardless of the co-existence of high concentrations of FeCl 3 (90 mM) and a high flow speed (4.0 mL/min). Based on these results, a separation process integrating SiPS-N(CH 3 ) 3 Cl and the matched parameters was finally developed and tested. Our work greatly raised the lead separation efficiency in HCl solutions with implications for measuring 210 Pb in environmental samples.
研究领域:
环境科学
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化学
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产品关联
DOI
高影响因子
RSC Advances
·
2017
·Vol. 7
·期 24
·14330-14336
·
IF 3.108
Minghao Li,Wenzhi Li,Yijuan Lu,Hasan Jameel,Hou-min Chang,Longlong Ma
Biomass derived 5-hydroxymethylfurfural (HMF) is regarded as an important platform molecule for the synthesis of value-added chemicals and fuels, but the high production cost has always been a bottleneck for the industrial scale use of HMF. Different mineral acids (HCl and H2SO4) being used as the catalyst and different salts being used as the reaction promoter were evaluated. It was found that HCl, in combination with NaCl, in a water/γ-valerolactone system showed high selectivity and impressive efficiency for the synthesis of HMF from glucose. The optimal conditions to obtain the best HMF yield (62.45%) were 0.2 M HCl and 0.1 M NaCl at 140 °C with a residence time of 60 minutes. An 18.22% molar yield of LA was obtained as a by-product. The effect of different anions was also investigated, and it was determined that not only the hydrogen ions, but also the nature of the acid and the type of salt played a joint role in improving the HMF yield. In addition, a possible synthesis pathway was proposed for large scale production of HMF.
研究领域:
生物化学
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可再生资源与环境科学
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DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2023
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IF 8.6
Jianwei Zhang,Ronghao Liu,Xiaoxia Liu,Jun Li,Ruihui Wu,Yanzhao Yang
Rhodium, as a rare precious metal, has always been a challenge for the chemical industry to efficiently recover rhodium by extraction due to the complex existing situation in hydrochloric acid medium. Herein, a strongly hydrophobic DABCO-based ionic liquid (IL) [C 8 DABCO][NTf 2 ] was designed and synthesized to construct a solvent-free extraction system of Rh(III) from high-concentration hydrochloric acid medium. At first, the effects of some important parameters on Rh(III) extraction were studied, such as equilibrium time, IL dosage, hydrochloric acid concentration, and initial Rh(III) concentration, the results showed that 81.54% Rh(III) can be extracted under the optimum extraction conditions. Based on the experimental run results, a quadratic model equation was established by using the response surface method (RSM), which can be used to calculate the amount that [C 8 DABCO][NTf 2 ] will be offered at various HCl concentrations during the actual extraction of Rh(III). Then, using Job's method, the Ultraviolet visible spectroscopy (UV–vis), Fourier transform infrared spectroscopy (FT-IR), Energy-dispersive X-ray spectroscopy (EDS), and Electrostatic potential (ESP) prove that the extraction mechanism is an anion exchange mechanism. Finally, in the mixed solution of multi-metals, the extraction efficiency of [C 8 DABCO][NTf 2 ] for Rh(III) is not disturbed, and the extraction efficiency for other metals is less than 1%. And the single-stage stripping efficiency of Rh(III) was up to 88% through HCl stripping, which solved the problem of difficult stripping of Rh(III) solution and realized the recycling of IL. The study provides a reliable and efficient way for recovering Rh(III) from high-concentrations HCl solutions.
研究领域:
化学工程
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材料科学
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产品关联
DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
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2022
·Vol. 46
·期 41
·19824-19833
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IF 3.925
Xiaoxia Liu,Yang Wu,Yangyang Wang,Huiying Wei,Jinxin Guo,Yanzhao Yang
Liquid–liquid extraction technology based on ionic liquids (ILs) is an efficient and environmentally friendly method to recover Au(III). This work aims to separate Au(III) from hydrochloric acid media using a novel IL [DBA-Pyr][NTf2], which is a pyrrolidinium-based IL functionalized with amide groups. Firstly, experiments have been carried out under optimal conditions, including the concentration, acidity and temperature. It turns out that low concentrations of hydrochloric acid help in Au(III) extraction, while the increase of chloride ion concentrations has an adverse effect. Then, through Job's method, extraction complexes with a molar ratio of [DBA-Pyr][NTf2]-to-Au(III) of 1 : 1 were determined. And, the anion exchange extraction mechanism was confirmed by FT-IR, UV-Vis, and 13C NMR spectroscopies and an electrostatic potential energy (ESP). Under the optimal extraction conditions, it has excellent selectivity to Au(III) compared to both base metal ions and platinum group metals (PGMs). Furthermore, Au(III) could also be recovered from the IL phase using an aqueous solution of thiourea in 95.6% with high selectivity. After 4 cycle experiments, an extraction efficiency of more than 90% is still maintained. The results show that [DBA-Pyr][NTf2] has potential application prospects in Au(III) recovery from hydrochloric acid media.
研究领域:
化学工程
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环境科学
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DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
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2024
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IF 13.3
Yangzhen Jin,Yebin Zhou,Pengze Zhang,Yi Liu,Chunshan Lu,Xiaonian Li
The catalytic alkaline dehydrochlorination process, characterized by high atom economy, stands as a prevalent method in the synthesis of valuable alkene halides. Nonetheless, the efficacy of ionic liquids (ILs) as catalysts for dehydrochlorination is hindered by challenges such as swift deactivation attributed to decomposition and reduced selectivity without clear causative factors. This investigation employs a systematic approach, integrating Density Functional Theory (DFT) simulations with experimental methodologies, to delve into the mechanisms of IL-catalyzed dehydrochlorination, aiming to elucidate both stabilization strategies and catalytic pathways. The examination of thermal decomposition rates is rooted in a meticulous assessment of the energy barriers associated with decomposition and dissociation processes. The active role of free Cl − is established, albeit its acidification by HCl, which results in diminished catalytic activity. To counteract this acidifying influence, a novel active site denoted as [Cl-KCl] − is conceptually devised to mitigate such effects. Through the strategic implementation of cationic fixation, the IL-KCl combination catalyst is synthesized and empirically confirmed to demonstrate augmented acid resistance while upholding a consistent reaction selectivity of approximately 85 %. This contrasts starkly with the declining catalytic selectivity observed with IL in isolation, plummeting from 85% to 65%. Consequently, the IL-KCl combination catalyst emerges as a promising option for alkali catalyzed dehydrochlorination, offering enhanced stability and sustained high selectivity throughout the catalytic process.
研究领域:
化学工程
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催化科学
✓ 已验证
产品关联
DOI
高影响因子
HYDROMETALLURGY
·
2024
·
IF 4.8
Ronghao Liu,Jun Li,Xiaoxia Liu,Xiaolu Yin,Yanzhao Yang
The effective and environmentally friendly recovery of gold from secondary resources has recently received increased attention. Hydrophobic deep eutectic solvent (HDES) composed of N , N -di-butylacetamide and 1-decanoic acid was used to construct the liquid-liquid extraction system to extract Au(III) from HCl medium. At first, DSC, TGA, FT-IR, and 1 H NMR were used to describe the evidence of internal hydrogen bond interaction. The above evidence was verified in the molecular dynamics study of HDES. Then, a series of optimization experiments were carried out to investigate the extraction behaviors of HDES. Based on the results of optimization experiments, response surface method was used to explore the best experimental conditions and the results showed that HDES extracted 99% Au(III) under 0.56 mol/L HCl, 2.19 mol/L NaCl, and 5.83 mmol/L Au(III), and the maximum loading reached 77.0 mg/g. Further studies on the kinetics and thermodynamics of the extraction were used to propose an ion association mechanism. In addition, using 0.1 mol/L thiourea as the stripping agent, HDES displayed outstanding Au(III) selectivity and maintained the extraction efficiency in tests which involved 5-cycles. Overall, this study provides a green and efficient Au(III) recovery strategy for secondary resources.
研究领域:
化学工程
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环境科学
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产品关联
DOI
高影响因子
PROCESS SAFETY AND ENVIRONMENTAL PROTECTION
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2024
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IF 6.9
Qiang Wang,Chun-guang Song,Hai-qing Hao,Meng Wang,Zong-yu Feng,Yong-qi Zhang,Xiang-xin Xue,Xiao-wei Huang
Wastewater recycling is the desired goal of the rare earth separation plants for current ecological requirements and economic benefit. The MgCl 2 wastewater generated during rare earth extraction and separation process was treated by spray pyrolysis for the first time to achieve full recycling. The kinetic of spray pyrolysis process and the mechanism affecting the activity of MgO powder were investigated. The results showed that the rate determining step of MgCl 2 solution spray pyrolysis was transformed from a chemical reaction control to a diffusion process control after the temperature exceeded 1073 K. The MgO powder prepared by spray pyrolysis was rough and porous, the embedding of Cl made MgO grains severely distorted, producing more defects. Meanwhile, polycrystalline basic magnesium chloride likewise had more defects. These two points resulted a higher density of defects of MgO powders, and causing higher activity. Moreover, at a temperature of 1173 K, MgCl 2 concentration of 300 g/L and N 2 flow rate of 40 L/min, the thermal decomposition rate of MgCl 2 reached 99.54%, the alkalinity of the powder reached 0.045 mol/g, and the iodine absorption value reached 102.72 mg I 2 /g MgO. Meanwhile, the high purity hydrochloric acid with a concentration of 6.70 mol/L was obtained.
研究领域:
环境科学
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材料科学
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化学工程
✓ 已验证
产品关联
DOI
高影响因子
ACS Applied Materials & Interfaces
·
2025
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IF 8.2
Wenqing Liang,Shengqiang Ren,Xia Hao,Cong Chen,Chao Ding,Jingquan Zhang,Shuyu Zhang,Dewei Zhao
Low-dimensional lead-free perovskite single crystals (SCs) have exhibited great potential in high-energy ionizing radiation detections owing to their outstanding sensitivity and charge transport properties. However, the preparation of chlorine-based SCs is more challenging due to their low solubility in organic solvents and acidic solutions. In this work, we report a universal growth strategy of hydrochloric acid-assisted temperature lowering for low-dimensional layered perovskite CsMnCl3·2H2O SCs. Compared with SCs prepared by solution evaporation crystallization, centimeter-sized SCs were achieved with ultrahigh crystal quality, showing a very small full width at half-maximum of 0.02° at the plane (002). Our layered perovskite CsMnCl3 2H2O X-ray detector shows unique anisotropic X-ray detecting performance at parallel and perpendicular to the (002) crystal plane. An ultralow detection limit of 9.3 nGyair s–1 has been obtained, which is significantly lower than the 5.5 μGyair s–1 required for regular medical diagnostics. Furthermore, the device shows enhanced stability with a slight degradation of 8% after storage in air ambient for 6 months. Our work suggests a promising approach to fabricate high-quality SCs for sensitive and stable X-ray detection applications.
研究领域:
材料科学
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辐射探测技术
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产品关联
DOI
PubMed
高影响因子
ChemCatChem
·
2022
·Vol. 14
·期 21
·e202200785
·
IF 5.497
Xianliang Qiao,Xinyu Liu,Yang Yang,Zhenhua Mao,Tianhe Li,Lele Gao,Chaoyue Zhao,Qingxin Guan,Wei Li
Graphical Acetylene hydrochlorination : Dicarbonyl ligands enhanced the dispersion of Au species, suppressed the reduction of Au cations, and reduced the formation of carbon deposits during catalytic acetylene hydrochlorination. Carbon-supported Au (Au/AC) has been proven to be one of the most promising catalysts in the field of acetylene hydrochlorination. However, the catalytic performance of conventional Au/AC catalyst is usually limited due to the unsatisfactory dispersion of active Au cation on the surface of the support, carbon deposition, and inevitable reduction to inactive Au nanoparticles. Herein, Au catalysts with highly dispersed Au cation were developed using the complexation of dicarbonyl ligand N-chlorosuccinimide (NCS) and N-methylsuccinimide (NMS). The obtained Au−NMS/AC and Au−NCS/AC catalysts with 0.1 wt.% Au loading possessed acetylene conversion of 98 % and 88 % at 180 °C and GHSV (C 2 H 2 ) of 160 h −1 , which were clearly better than that of pristine Au/AC. The characterization results showed that coordination between Au cation and ligands enhanced the dispersion of Au species, suppressed the reduction of Au cation, and reduced the formation of carbon deposits. Density functional theory (DFT) calculations suggest that Au−NMS/AC and Au−NCS/AC catalysts follow a HCl-preferred concerted addition reaction mechanism with lower reaction energy barrier. This favors the high activity and nuclearity stability of the Au center. This study provides great potential for the use of dicarbonyl ligands on Au-based catalysts in acetylene hydrochlorination.
研究领域:
催化化学
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材料科学
✓ 已验证
产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2021
·
IF 7.312
Ping Lv,Ronghao Liu,Yangyang Wang,Xiaoxia Liu,Yang Wu,Wenfeng Xue,Yanzhao Yang
In this study, a novel gemini-type benzimidazole ionic liquid [C 6 BIM 2 ][NTf 2 ] 2 was synthesized for efficient extract gold(III) from hydrochloric acid medium. Firstly, a series of parameters (e.g., vibrating time, the extractant concentration, acidity and salinity) were optimized and obtained the optimal extraction condition. Under this condition, the extraction efficiency can reach 98.42%, along with the distribution ratio of 186.87. Through the response surface methodology (RSM) model optimization, the amount of [C 6 BIM 2 ][NTf 2 ] 2 corresponding to different HCl concentration was determined for gold(III) extraction during actual operation. Then, verified the anion exchange mechanism with the aid of Job’s method, UV–vis, FT-IR and 13 C NMR. Thermodynamic parameters were calculated and implied that the extraction reaction was an exothermic and spontaneous process. Furthermore, organic phase loaded with gold(III) was easy to be completely stripped by CS(NH 2 ) 2 / HCl solution and its extraction ability was kept constant after 5 cycles extraction experiments. Meanwhile, [C 6 BIM 2 ][NTf 2 ] 2 has a superb ability to select gold(III) in the multi-metal solution. In general, [C 6 BIM 2 ][NTf 2 ] 2 showed distinguished selectivity and extraction ability for gold(III) from secondary resources, which was claimed to be a promising new style extractant.
研究领域:
化学工程
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材料科学
✓ 已验证
DOI
高影响因子
POLYMER DEGRADATION AND STABILITY
·
2014
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IF 2.633
Guoan Chen,Liqiang Gu,Youwei Yao
A Zn-containing complex ([ZnL 2 ]· x H 2 O, x ≈ 4, abbreviated as ZnL 2 ; HL = 1,3-dihydroxy-2-hydroxymethyl-2-(salicylidimino)propane) was synthesized and used as a thermal stabilizer . Through discoloration and dehydrochlorination tests at 180 °C, ZnL 2 was proved to be a co-stabilizer of long-term thermal stability for poly(vinyl chloride) (PVC): compared with the PVC samples stabilized using typical metallic soap stabilizers with the mass ratio of calcium stearate (CaSt 2 ) to zinc stearate (ZnSt 2 ) ranging from 1.5/0 to 0/1.5, whose induction time ( t i ), stability time ( t s ) respectively ranged from 9 to 54 min, from 12 to 56 min, the PVC samples stabilized using combinations with the mass ratio of CaSt 2 to ZnL 2 from 1.5/0 to 0/1.5 showed apparent thermal stability with t i , t s ranging from 44 to 85 min, from 49 to 88 min. PVC sample (PVC resin = 50.0 g, ZnL 2 = 1.5 g, pentaerythritol = 0.3 g, dioctyl phthalate = 2.5 g) displayed a significant long-term thermal stability with t i of 102 min, t s of 105 min, and totally-turning-black time of 170 min.
研究领域:
材料科学
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化学工程
✓ 已验证
DOI
高影响因子
POLYMER DEGRADATION AND STABILITY
·
2018
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IF 3.193
Bozhen Wu,Yating Wang,Si Chen,Muyan Wang,Meng Ma,Yanqin Shi,Xu Wang
A novel kind of poly(vinyl chloride) (PVC) thermal stabilizer , zinc dehydroacetate (ZnL 2 ), was designed and synthesized using zinc acetate and dehydroacetic acid (DA) as raw materials, which had a unique "zinc burning" inhibition synergistic effect with calcium stearate (CaSt 2 ) that was 8 times greater than that of the CaSt 2 /ZnSt 2 combination reference stabilizer . The structure and stability of ZnL 2 were confirmed by Fourier-transform infrared, elemental analysis , and thermogravimetric analysis . The stability distinction of ZnL 2 and ZnSt 2 , and the stable effect of the two systems after being combined with CaSt 2 , were investigated by the Congo red test, solution acidity test, and discoloration test. The results showed that in the Congo red test the stability time of ZnL 2 was 8.9 min, which was 1.3 times that of ZnSt 2 , and the stability time of ZnL 2 /CaSt 2 was 13 min, which was 1.4 times that of a traditional Ca/Zn stabilizer. Furthermore, the stability time of ZnL 2 was 36 min in the solution acidity test, which was 2 times higher than that of ZnSt 2 , and the stability time was increased to 196 min after combining it with CaSt 2 , which was 8 times greater than that of the Ca/Zn stabilizer. Moreover, the dehydrochlorination rate of PVC stabilized with ZnL 2 was slower than with other stabilizers. The system with ZnL 2 /CaSt 2 could effectively delay “zinc burning” because of the excellent synergistic effect in the thermal aging test, with a stability time as long as 140 min. At the same time, the mechanism of PVC stabilization by ZnL 2 was studied in two simple experiments, and the stabilization mechanism of ZnL 2 in PVC degradation was speculated on.
研究领域:
材料科学
·
化学工程
✓ 已验证
DOI
高影响因子