A silver-based metal-organic framework（Ag-MOFs）, [Ag2（H3 ddcba）（dpp）2]（1）（H5 ddcba = 3,5-（di（2’,5’-dicarboxylphenyl）benozoic acid, dpp = 1,3-di（4-pyridyl）propane）, was successfully constructed via hyd...A silver-based metal-organic framework（Ag-MOFs）, [Ag2（H3 ddcba）（dpp）2]（1）（H5 ddcba = 3,5-（di（2’,5’-dicarboxylphenyl）benozoic acid, dpp = 1,3-di（4-pyridyl）propane）, was successfully constructed via hydrothermal assembly of a pentacaboxylate ligand, a N-donor ligand and Ag（I） ions, which possesses a pcu topology and exhibits excellent catalytic properties in aqueous solution for the degradation of onitrophenol（2-NP）, m-nitrophenol（3-NP） and p-nitrophenol（4-NP）. Related kinetics of such catalytic reactions, photoluminescent and thermal stability of compound 1 were also investigated.展开更多
Devising a desirable adsorbent for efficiently selective capture of Ag(Ⅰ) from wastewater has attracted much attention but faced with huge challenges. Herein, a novel linear o-phenanthroline-based polymer L-PRL was p...Devising a desirable adsorbent for efficiently selective capture of Ag(Ⅰ) from wastewater has attracted much attention but faced with huge challenges. Herein, a novel linear o-phenanthroline-based polymer L-PRL was prepared via chemical oxidative polymerization for the adsorption of Ag(Ⅰ). The maximum adsorption capacity for Ag(Ⅰ) by L-PRL is 325.8 mg/g at pH 0. In addition, L-PRL owes ascendant selectivity for Ag(Ⅰ) from aqueous solutions containing various interfering metal ions of Pb(Ⅱ), Co(Ⅱ), Ni(Ⅱ), Cd(Ⅱ)and Fe(Ⅲ). Multiple characterizations of FT-IR and XPS uncover that the N groups on L-PRL act as adsorption sites to coordinate with Ag(Ⅰ). Density functional theory(DFT) calculations further evidence the mechanism that L-PRL is provided with the admirable adsorptivity and selectivity for Ag(Ⅰ). It is mainly attributed to the most stable complexes of L-PRL with Ag(Ⅰ), which possesses shortest Ag-N bond length compared with other heavy metal ions. Furthermore, 93.5% of initial adsorption capacity is reserved after four continuous regeneration cycles, indicating that L-PRL is equipped with superior recyclability and durability, and L-PRL is capable of removing Ag(Ⅰ) in low-concentration actual Ag(Ⅰ)-containing wastewater completely. This study shed light on the rational design of polymer adsorbents and in-depth insight into selective removal of aqueous Ag(Ⅰ).展开更多
A novel chelating resin (PETU) with thiourea groups in its main chain was synthesized by the reaction of O,O'-butane-1,4-diyl dicarbonisothiocyanatidate and triethylene tetraamine. The adsorption of Ag(I) on PETU ...A novel chelating resin (PETU) with thiourea groups in its main chain was synthesized by the reaction of O,O'-butane-1,4-diyl dicarbonisothiocyanatidate and triethylene tetraamine. The adsorption of Ag(I) on PETU was investigated by batch tests. The results showed that adsorption data fitted Boyd's diffusion equation of liquid film and the adsorption was controlled by liquid film diffusion. Under the temperatures between 15～60 ℃, the adsorption capacity decreased with the increase of temperature, and increased with the increase of initial concentration of Ag(I). The experimental data fitted Langmuir and Freundlich equations, and the correlation coefficients for Langmuir equation were between 0.9965～0.9998, and those for Freundlich equation were between 0.8211～0.9810, and increased with the adsorption temperature. △H, △G and △S calculated by thermodynamic formulae were all negative, which meant that the adsorption process was exothermic and spontaneous, and the entropy decreased during the process. XPS results showed that N, S and O atoms were the electron donors to coordinate with Ag.展开更多
基金financial support from the National Science Foundation of China (Nos. 216731272, 2137312, 21671119, 51572152 and 51502155)
文摘A silver-based metal-organic framework（Ag-MOFs）, [Ag2（H3 ddcba）（dpp）2]（1）（H5 ddcba = 3,5-（di（2’,5’-dicarboxylphenyl）benozoic acid, dpp = 1,3-di（4-pyridyl）propane）, was successfully constructed via hydrothermal assembly of a pentacaboxylate ligand, a N-donor ligand and Ag（I） ions, which possesses a pcu topology and exhibits excellent catalytic properties in aqueous solution for the degradation of onitrophenol（2-NP）, m-nitrophenol（3-NP） and p-nitrophenol（4-NP）. Related kinetics of such catalytic reactions, photoluminescent and thermal stability of compound 1 were also investigated.
基金financially supported by the National Science Fund for Distinguished Young Scholars(No.52125002)the National Science Foundation of China(No.52100043)+1 种基金the National Key Research and Development Program of China(No.2019YFC1907900)the National Science Foundation of Jiangxi Province(No.20202BABL213037)。
文摘Devising a desirable adsorbent for efficiently selective capture of Ag(Ⅰ) from wastewater has attracted much attention but faced with huge challenges. Herein, a novel linear o-phenanthroline-based polymer L-PRL was prepared via chemical oxidative polymerization for the adsorption of Ag(Ⅰ). The maximum adsorption capacity for Ag(Ⅰ) by L-PRL is 325.8 mg/g at pH 0. In addition, L-PRL owes ascendant selectivity for Ag(Ⅰ) from aqueous solutions containing various interfering metal ions of Pb(Ⅱ), Co(Ⅱ), Ni(Ⅱ), Cd(Ⅱ)and Fe(Ⅲ). Multiple characterizations of FT-IR and XPS uncover that the N groups on L-PRL act as adsorption sites to coordinate with Ag(Ⅰ). Density functional theory(DFT) calculations further evidence the mechanism that L-PRL is provided with the admirable adsorptivity and selectivity for Ag(Ⅰ). It is mainly attributed to the most stable complexes of L-PRL with Ag(Ⅰ), which possesses shortest Ag-N bond length compared with other heavy metal ions. Furthermore, 93.5% of initial adsorption capacity is reserved after four continuous regeneration cycles, indicating that L-PRL is equipped with superior recyclability and durability, and L-PRL is capable of removing Ag(Ⅰ) in low-concentration actual Ag(Ⅰ)-containing wastewater completely. This study shed light on the rational design of polymer adsorbents and in-depth insight into selective removal of aqueous Ag(Ⅰ).
基金Supported by National Natural Science Foundation of China (No. 20476105)
文摘A novel chelating resin (PETU) with thiourea groups in its main chain was synthesized by the reaction of O,O'-butane-1,4-diyl dicarbonisothiocyanatidate and triethylene tetraamine. The adsorption of Ag(I) on PETU was investigated by batch tests. The results showed that adsorption data fitted Boyd's diffusion equation of liquid film and the adsorption was controlled by liquid film diffusion. Under the temperatures between 15～60 ℃, the adsorption capacity decreased with the increase of temperature, and increased with the increase of initial concentration of Ag(I). The experimental data fitted Langmuir and Freundlich equations, and the correlation coefficients for Langmuir equation were between 0.9965～0.9998, and those for Freundlich equation were between 0.8211～0.9810, and increased with the adsorption temperature. △H, △G and △S calculated by thermodynamic formulae were all negative, which meant that the adsorption process was exothermic and spontaneous, and the entropy decreased during the process. XPS results showed that N, S and O atoms were the electron donors to coordinate with Ag.
