Catalysis Science & Technology
·
2015
·Vol. 6
·期 11
·3854-3861
·
IF 5.426
Peng Wang,Huan Liu,Yong-Qi Li,Xiao-Li Zhao,Yong Lu,Ye Liu
A series of ionic phosphonium-based aminophosphines L1–L3 were prepared and fully characterized, in each of which the involved bifunctional moieties of the phosphine fragment and Lewis acidic phosphonium were linked together by stable chemical bonds and bridged by one N-atom. The molecular structure of the L2-ligated Rh-complex (Rh-L2) indicated that such bifunctionalities were well retained without incompatibility problems. Investigations on co-catalysis over L1–L3 showed that L3 exhibited the best sequential catalysis for both hydroformylation and acetalization. The phosphine fragment in L3 was responsible for hydroformylation together with the Rh-complex and the phosphonium acted as the Lewis acidic catalyst in charge of acetalization. The L3–Rh(acac)(CO)2 system also exhibited good generality to hydroformylation–acetalization of a wide range of olefins in different alcohols.
研究领域:
有机化学
·
催化化学
✓ 已验证
DOI
高影响因子
SCIENCE OF THE TOTAL ENVIRONMENT
·
2022
·
IF 10.753
Xiaoqin Nie,Yujing Zhang,Yating Jiang,Ning Pan,Chang Liu,Junling Wang,Chunyan Ma,Xue Xia,Mingxue Liu,Hongping Zhang,Xiaoan Li,Faqin Dong
The enrichment and recovery of U(VI) from low-level radioactive wastewater in the process of uranium enrichment is important for the sustainable development of nuclear energy and environmental protection. Herein, a novel amine-aminophosphonate bifunctionalized polyacrylonitrile fiber (AAP-PAN), was prepared for the extraction of U(VI) from simulated and real uranium-containing process wastewater. The AAP-PAN fiber demonstrated a maximum adsorption capacity of 313.6 mg g −1 at pH = 6.0 and 318 K in the batch experiments. During the dynamic column experiment, over 99.99% removal of U(VI) could be achieved by the fiber using multi-ion simulated solution and real wastewater with an excellent saturation adsorption capacity of 132.0 mg g −1 and 72.5 mg g −1 , respectively. It also exhibited an outstanding reusability for at least 5 cycles of adsorption process. The mechanism for U(VI) removal was studied by Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy analysis in the assist of simulation calculation. It suggested that the amine and aminophosphonate groups can easily bind uranyl ions due to U(VI) is more likely to combine with oxygen atoms of C O and P O, respectively.
研究领域:
环境科学
·
核能工程
·
材料科学
✓ 已验证
DOI
PubMed
高影响因子
HYDROMETALLURGY
·
2016
·
IF 2.29
Shengting Kuang,Zhifeng Zhang,Yanling Li,Guolong Wu,Haiqin Wei,Wuping Liao
A novel extractant, di (2-ethylhexyl) (2-((2-ethylhexyl) amino) propan-2-yl) phosphonate (DEHAPP, abbreviated as B ), was synthesized for the selective extraction of Ce(IV) in sulfate medium. The effect of contact time, the H 2 SO 4 concentration, the DEHAPP concentration and temperature on the Ce(IV) extraction were studied systematically. DEHAPP exhibits a good extraction ability towards Ce(IV) when compared with other neutral organophosphorus extractants such as Cyanex 923, Cyanex 925 and DEHEHP. The extraction equilibrium constants and thermodynamic parameters (Δ G , Δ H and Δ S ) were calculated. The extraction reaction of Ce(IV) is an endothermic process. The extracted complexes were determined to be H 2 SO 4 · B ( org ) and Ce(HSO 4 ) 2 SO 4 ·2 B ( org ) . A extraction process to selectively recover Ce(IV) from bastnaesite leaching was proposed, by which the purity of cerium product reached 99.5% with a yield of 90.7%.
研究领域:
化学工程
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2023
·
IF 8.6
Enas A. Imam,Ahmed I Hashem,Ahmad A. Tolba,Mohammad G. Mahfouz,Ibrahim El-Tantawy El-Sayed,Hamada B. Hawash,Rana R. Neiber,Hamed I. Mira,Ahmed A. Galhoum,Eric Guibal
Two aminophosphonate matrices (mono-aminophopshonate, MAP, and bi-aminophosphonate, BAP) are synthesized, varying the molar proportions of three precursors (thiocarbazide, p-phthalaldehyde, and triphenylphosphite). Nano-composites (CuO-MAP and CuO-BAP) are successfully elaborated by impregnation of the matrices with copper sulfate solution before processing to in situ precipitation of copper in alkaline solution (simultaneous partial Cu reduction). The sorbents are characterized using: TEM, XRD, elemental analysis, SEM-EDX, BET, titration (pH PZC ), XPS and FTIR analyses. Uranium sorption properties are compared for the different sorbents through the study of pH effect (optimum close to 4.5), the uptake kinetics (equilibrium reached in 60 min) and sorption isotherms. Uptake kinetics are finely fitted by the pseudo-second order rate equation (and the resistance to intraparticle diffusion). The sorption isotherms are modeled by the Langmuir equation with maximum sorption capacity (mmol U g −1 ) decreasing according to CuO-BAP(1.15) ≫ CuO-MAP(0.80) > BAP(0.74) ≫ MAP(0.50). The enhanced textural properties and the increase in the density of sorption sites (probably completed by a better steric arrangement for improved reactivity) may explain this ranking. The sorption is endothermic: sorption capacity and affinity coefficient increase with temperature. Uranium is readily desorbed from loaded-sorbents (efficiency > 98 %) using either HCl (0.2 M) solution or acidified urea (0.25 M) solution (pH 2.5) for aminophosphonate matrices and nano-composites, respectively. The type of sorbent does not affect the stability at recycling: at the sixth cycle, the loss in sorption and desorption performances varies by 6.2–7 % and 4.2–4.9 %, respectively. CuO-BAP sorbent shows high potential for uranium recovery from complex acid ore leachate. The broad spectrum of bound metals does not allow producing a pure yellow cake after ammonia precipitation of eluate (containing up to 15–22 % impurities).
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 Saudi Chemical Society
·
2022
·
IF 4.712
Tao Chen,Ning Sun,Yuan Zhao,Jie Gao,Guowen Hu,Xiaobing Han,Yayang Tian,Linfeng Chen,Guobao Huang,Bing Li
A new aminophosphonic acid chelating resin was successfully prepared via electron beam irradiation grafting combined with chemical modification and used for the efficient removal of La(III). Firstly, glycidyl methacrylate (GMA) was grafted to polystyrene microspheres (PS) via electron beam co-radiation to obtain PS-PGMA microspheres, then followed by the amination with diethylenetriamine (DETA) to formed PS-PGMA-DETA (PGD) microspheres through nucleophilic substitution between amino and epoxy group, and finally PS-PGMA-DETA-PA (PGDP) microspheres was obtained by phosphorylation with phosphorous acid (PA). The obtained chelating resin absorbent was characterized by Fourier-transform infrared (FT-IR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), which demonstrated that the millimetric aminophosphonic acid chelating resin were successfully prepared with well-defined morphology and enhanced thermal stability. The X-ray photoelectron spectroscopy (XPS) characterization results confirmed a possible adsorption mechanism, which is mainly based on the chelation and coordination of N and O in PDGP with La(III) in the solution. A series of parameters were taken into account in the adsorption experiment, such as absorbed dose, GMA concentration, dosage of PGDP, pH, contact time, temperature, and the initial concentrations of La(III). The maximum adsorption capacity obtained from the research can be achieved 288.69 mg/g at 298.15 K, pH = 6. The kinetic sorption for for La(III) fitted the type 1 pseudo-second-order (R 2 = 0.9981), which revealed that the La(III) are chemisorbed on the surface of the PGDP. It was concluded that the La(III) adsorption conformed to the Freundlich equation, indicating a multilayer adsorption process. Thermodynamic data indicated that the La(III) uptake process was a spontaneous and endothermic. In addition, this research provided a new irradiation grafting method for rare earth ions removal.
研究领域:
材料科学
·
环境科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2024
·
IF 7.4
Ibrahim El-Tantawy El-Sayed,Xingmei Lu,Jiayu Xin,Azza A. Al-Ghamdi,Enas A. Imam,Hamada B. Hawash,Ahmed A. Galhoum,S. Wageh
Two α-aminophosphonate anlages (methyl- and phenyl-derivatives, MeAP and PhAP, respectively) were synthesized via an in-situ reaction. Moreover, their corresponding sand nanocomposites, MeAPNC and PhAPNC, respectively, were prepared using an eco-friendly, inexpensive and facile solid-state synthetic route. These materials were extensively characterized by CHNSP/O, XRD, FTIR, SEM-EDX, TEM, and PZC. Lanthanum sorption characteristics were investigated and compared through the study of pH dependence (optimal pH: 4.5), equilibration time (achieved at 120 and 90 min for α-APs and nanocomposites, respectively), and sorption isotherms. The Sips isotherm and pseudo-second-order (PSORE) kinetics were the optimal models for fitting the experimental data. Sorption isotherms showed that methyl-derivatives (≈1.29–1.359 mmol/g) were more effective than their corresponding phenyl-derivatives (≈0.941–0.986 mmol/g) due to steric hindrance, acid-base differences, and inductive effects. Sorbents showed appreciated stability with just a 4.5–10.5 % loss in performance over six reuse cycles using HCl (0.2 M). Notably, sand incorporation slightly increased capacity with half-organic-portion in composites, as well as enhanced kinetics and regeneration efficiency. La(III) sorption is spontaneous, exothermic, and increases randomness across all sorbents. Finally, the prepared sorbents have proven effective sorption for Nd(III) beside La(III) with high selectivity from acidic complex monazite liquor.
研究领域:
材料科学
·
环境科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
Polymer Chemistry
·
2013
·Vol. 5
·期 6
·1857-1862
·
IF 5.231
Yaling Zhang,Yuan Zhao,Bin Yang,Chongyu Zhu,Yen Wei,Lei Tao
A multicomponent reaction (MCR) has been carried out on the platform of controlled radical polymerization (CRP) to construct a ‘one pot’ MCR-CRP system for the facile preparation of well-defined functional polymers. In the current work, a novel ‘one pot’ system has been built through a combination of the Kabachnik–Fields (KF) reaction and reversible addition fragmentation chain transfer (RAFT) polymerization. Compared to a traditional stepwise method and polymer post-polymerization modification, this novel ‘one pot’ system exhibited distinct advantages to much more facilely and efficiently prepared well-defined poly(aminophosphonate)s (polyAPPs). A series of unique polyAPPs have also been successfully prepared through this KF–RAFT system, suggesting this novel method is a general and versatile approach to prepare well-defined organophosphorous polymers.
研究领域:
高分子化学
·
材料科学
✓ 已验证
DOI
高影响因子
RSC Advances
·
2025
·Vol. 15
·期 7
·5042-5059
·
IF 4.6
Irfan Ijaz,Aysha Bukhari,Ammara Nazir,Ezaz Gilani,Hina Zain,Attia Shaheen,Mohammed Rafi Shaik,Mujeeb Khan,Jilani P. Shaik
The simultaneous removal of antibiotics and heavy metal ions is of utmost importance because of their hazardous effects on the environment and humans. For the adsorption of sulfamethoxazole (SMX) and neodymium (Nd3+) in mono- and binary contaminant systems (SMX–Nd3+ and Nd3+–SMX), a novel composite was designed using sulfated fucan (FuS), MXenes, and α-aminophosphonates (AMPs) in this study. As far as we know, the concurrent adsorption of SMX and Nd3+ employing materials made of MXenes, FuS, and AMPs with this specific structure has not yet been reported. At 318 K, the FuS@MXene@AMP adsorbent demonstrated excellent adsorption capacities of 448.91 and 255.78 mg g−1 for SMX and Nd3+, respectively. The pseudo-first-order (PSO) kinetic model was the most appropriate for depicting the adsorption of SMX and Nd3+ among all the tested kinetic models. The adsorption of SMX and Nd3+ is better described by the Langmuir isotherm model with a higher value of adsorption capacity and R2. The simultaneous presence of Nd3+ and SMX promoted mutual sorption between the antibiotic and metal ions in the binary systems. The results of FTIR and XPS studies indicated that the removal mechanisms were primarily due to hydrogen bonding, complexation, electrostatic interaction, and π–π interaction.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2022
·
IF 16.744
Rana R. Neiber,Ahmed A. Galhoum,Ibrahim El-Tantawy El Sayed,Eric Guibal,Jiayu Xin,Xingmei Lu
A one-pot synthesis procedure is designed for preparing two α-aminophosphonate-based-sorbents (DA and TA sorbents). The reaction takes place between amine precursors (two different aliphatic amines with different chain lengths and amino group content; i.e., ethylenediamine (DA) or diethylenetriamine (TA), respectively) and both salicylaldehyde and diphenyl phosphite. Ionic liquid may be used under controlled conditions as an alternative to TiCl 4 catalyst. These materials are first characterized by SEM-EDX, AFM, BET, XRD, FTIR, 1 H-, 13 C-, and 31 P NMR, XPS, TGA, elemental analysis (CHNP), and titration (PZC). Combined with the study of pH effect on Pb(II) sorption, FTIR and XPS analyses are used for exploring the mechanisms involved in metal binding. In a second step, the sorption properties are compared for Pb(II) recovery at pH ≈5. Maximum sorption is influenced by the length of the chain: DA (0.694 mmol Pb g −1 ) > TA (0.494 mmol Pb g −1 ). The sorption isotherms are modelled by the Sips equation for DA (and the Langmuir Dual Site equation) and by the Langmuir equation for TA. Thermodynamic parameters (ΔG°, ΔH° and ΔS°) indicate the spontaneous, endothermic nature and randomness increases during the sorption process. The uptake kinetics (equilibrium reached ≈120 min) is almost equally fitted by the pseudo-first-order rate equation and the pseudo-second-order rate equation. The sorbents show selective Pb(II) sorption against heavy base metals in multi-component solutions. QSAR tools (quantitative activity structure–activity relationships) are used for evaluating the correlation between their intrinsic metal characteristics and their affinities for sorbents. The sorbents are efficiently recycled for at least 5 cycles using 0.2 M HCl as the eluent (loss in sorption and desorption performances ≈10-14% at the fifth cycle, compared with the first cycle).
研究领域:
化学工程
·
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
Arabian Journal of Chemistry
·
2023
·
IF 6
Zhujuan Li,Shuliang Chen,Futing Zi,Xianzhi Hu,Yunlong Chen
A fast and efficient Au (I) recovery adsorption method from an actual leaching solution of Cu 2+ -en-S 2 O 3 2- is presented. Aminophosphonic acid derivatized polyacrylonitrile fibers (PAN-NP), prepared with triethylenetetramine and phosphoric acid by chemical grafting, were used as the adsorbent. The adsorbent was well characterized by FT-IR, SEM, TGA and XPS. The effects of contact time, pH, temperature, and Au (Ⅰ) concentration were also investigated. PAN-NP can rapidly capture Au(S 2 O 3 ) 2 3– (20 min) and has a maximum adsorption capacity of 14.68 kg/t. Compared with -SH modified, PAN-NP has better stability and without oxidized. The adsorption process was described based on the Langmuir isothermal model ( R 2 > 0.99). Thermodynamic parameters indicated that the adsorption of Au(S 2 O 3 ) 2 3– on PAN-NP was exothermic ( ΔH θ = −9.906 kJ/mol) and adsorption mechanism involved a collective effect resulting the anion exchange of Au(S 2 O 3 ) 2 3– with –RNH 3 + H 2 PO 3 - , electrostatic attraction between –RNH 3 + and Au(S 2 O 3 ) 2 3– and complexation of P = O with Au (Ⅰ). Besides, PAN-NP-Au can be effectively eluted by sodium sulfite. Importantly, in the Cu 2+ -en-S 2 O 3 2- actual leaching solution, the PAN-NP can efficiently recover Au (I) with an adsorption percentage of up to 97 % at a the solidliquid ratio of 1:50, thereby affording a satisfactory application result. This is a meaningful method for recovering Au (Ⅰ) from thiosulfate solution.
研究领域:
材料科学
·
环境工程
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Jie Zhou,Xuyi Zhang,Bicheng Deng,Yabin Huang,Xiaojuan Liu,Shunyan Ning,Shengting Kuang,Wuping Liao
High-purity heavy rare earths (HREs) are important for promoting the development of cutting-edge materials, but their efficient separation and purification still face significant challenges. Here, a silica/polymer-based β-aminophosphonic acid resin (HEHAEP/SiO 2 -P) was prepared by vacuum impregnation for the separation of HREs from chloride media. At pH = 2.0, the separation factors ( SF ) for Er/Ho, Tm/Er, Yb/Tm and Lu/Yb were 2.35, 3.62, 3.14 and 1.23, respectively, surpassing those of some other reported impregnating resins. The maximum adsorption capacity of HEHAEP/SiO 2 -P for Ho, Er, Tm, Yb and Lu were 33.5, 34.6, 37.0, 38.3 and 43.2 mg/g, respectively. The adsorption process was characterized as homogeneous monolayer chemisorption, driven by entropy in a spontaneous endothermic reaction. Complete desorption of the adsorbed HREs was achieved using 4.0 mol/L HNO 3 . Employing our strategy, as exemplified by Tm, high-purity Tm 2 O 3 (99.997 %) was obtained by HEHAEP/SiO 2 -P resin in the column chromatography separation system. FT-IR and XPS analysis demonstrated that both P-OH and P O groups participated in the coordination reaction during the HREs adsorption.
研究领域:
材料科学
·
化学工程
✓ 已验证
DOI
高影响因子
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
·
2016
·
IF 2.857
Guoping Zhang,Gefei Hao,Jianke Pan,Jian Zhang,Deyu Hu,Baoan Song
The asymmetric synthesis of enantiomerically pure α-aminophosphonates with high and bioselective activities is a challenge. Here, we report that both enantiomers of α-aminophosphonates bearing the N-benzothiazole moiety can be prepared in high yields (up to 99%) and excellent enantioselectivities (up to 99% ee) by using chiral thiourea organocatalysts. Evaluation of the antiviral activities of our reaction products against cucumber mosaic virus (CMV) led to promising hits with high and selective biological activities, wherein (R)-enantiomers exhibit higher biological activities than the corresponding (S)-enantiomers. Especially, compound (R)-3b with excellent anti-CMV activity (curative activity, 72.3%; protection activity, 56.9%; and inactivation activity, 96.9%) at 500 μg/mL emerged as a potential inhibitor of the plant virus. The difference in the selective bioactivity could be affected by the combination mode of the three-dimensional space between the enantiomers of α-aminophosphonate and cucumber mosaic virus coat protein (CMV-CP) via florescence spectroscopy and molecular docking.
研究领域:
有机化学
·
生物化学
·
植物病理学
✓ 已验证
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）