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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2023 · IF 8.2

Preparation of polyamidoamine dendrimer-functionalized chitosan beads for the removal of Ag(I), Cu(II), and Pb(II)

Xiaoqi Liu,Yanyun Zhang,Yan Liu,Ting'an Zhang

Chitosan bead grafted by third-generation dendrimers (CB-G3) with a diameter of 1.40 mm was synthesized to investigate their performance in recovering Ag(I), Cu(II), and Pb(II) ions in aqueous media. The prepared adsorbents were characterized by XRD, FT-IR, elemental analysis, TGA , and SEM, and the effects of pH, contact time, concentration, and temperature were examined. The results showed that the adsorbents were successfully fabricated. The optimum pH value was 5, and the increased generation number contributed to adsorption capacity improvement, indicating that electrostatic interactions between amine groups and metal ions are the governing mechanism of adsorption by the CB-G3. The kinetics, isotherms, and thermodynamics of Ag(I), Cu(II), and Pb(II) adsorption onto the CB-G3 were investigated. The adsorption processes can be described using pseudo-second-order kinetic and Langmuir models. The maximum monolayer adsorption capacities were 105.62, 88.82, and 97.87 mg·g −1 for Ag(I), Cu(II), and Pb(II) at 30 °C within 210 min, respectively. Electrostatic interactions and hydrogen bonds are the main mechanisms between metal ions and N atoms. Therefore, the CB-G3 is a promising candidate for Ag(I), Cu(II), and Pb(II) adsorption owing to its splendid ability in easy separation, good adsorptivity, and reusability for efficiently adsorbing Ag(I), Cu(II), and Pb(II) ions.

CAS / MDL: 2530-83-8
研究领域: 环境科学 · 材料科学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2017 · IF 2.714

In situ synthesis of AgNPs@Ag(I)-AMTD metal-organic gel composite and its catalytic properties

Yong Cheng,Feifei Sun,Qichun Feng,Qiang Zhao,Yinghua Zhou

In this study, we describe the successful fabrication of silver nanoparticles (AgNPs) within Ag(I)-AMTD metal-organic gel matrix. The resulting composite (AgNPs@Ag(I)-AMTD) was characterized by 1 H NMR, IR, SPR, SEM, TEM, EDX, XPS, and XRD. This material exhibited a remarkable and durable activity for the catalytic reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) and other nitroarenes by NaBH 4 in aqueous solution. This method affords a facile means of embedding the active silver nanoparticles within the metal-organic gel matrix and offers the necessary stability of the resulting silver nanostructure for catalytic transformation.

研究领域: 材料科学 · 催化化学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2021 · IF 7.312

Synthesis of novel sulfydryl-functionalized chelating adsorbent and its application for selective adsorption of Ag(I) under high acid

Xiao-Han Pan,Ling-Xiao Fu,Huan Wang,Yi Xue,Jian-Hua Zu

A novel sulfydryl-functionalized adsorbent PP-g-GMA@MEA for recovery of Ag(I) was synthesized by γ-ray induced simultaneous grafting of glycidyl methacrylate (GMA) onto polypropylene (PP) non-woven fabric, followed by ring-opening processes with mercaptoethylamine (MEA). The obtained adsorbents before and after adsorption of Ag(I) were fully characterized by SEM, EDS, FT-IR spectra, XRD and XPS. Batch adsorption experiments were carried out to evaluate adsorption abilities of the adsorbents under high acidity. The adsorption kinetics of Ag(I) were well fitted with pseudo-second-order kinetics model. The maximum adsorption capacity calculated by the Langmuir isotherm model was 262.51 mg/g at 25 °C. EDS, XRD and XPS analyses confirmed the mechanism of adsorption under high acidity was chelating reaction between -SH and Ag(I) and ion exchange adsorption towards [Ag(NO 3 ) 2 ] −1 . Through competitive adsorption tests, the PP-g-GMA@MEA was found remarkably selective towards Ag(I) when it coexisted with Cu(II), Co(II), Ni(II) and Cr(III) in high acidity medium. Therefore, the developed PP-g-GMA@MEA composite would be a promising adsorbent for Ag(I) recovery from industrial effluents.

研究领域: 环境科学 · 材料科学
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PROGRESS IN ORGANIC COATINGS · 2025 · IF 7.3

Slippery organogel coating based on Ag(I)-imine coordination bonding for enhanced self-healing, antifouling and anticorrosion properties

Yuan Jing,Fandi Meng,Fuhui Wang,Li Liu

Slippery liquid-infused porous surface (SLIPS) has garnered significant attention in marine anticorrosion and antifouling applications due to their slippery attributes. Nevertheless, it remains challenging to fulfill the protection requirements by relying exclusively on the barrier and anti-adhesion mechanisms of surface lubricating layer. In this work, a dual-functional slippery organogel coating was meticulously synthesized by introducing Ag(Ӏ)-imine coordination bonds into organosilicon networks, thereby endowing the coating with self-healing and antibacterial properties. A surface scratch with a width of 50 μm can be effectively repaired within 6 h at 60 °C, and the repair efficiency exceeds 85 %. In addition, the coating exhibits a dual antibacterial mechanism, which functions through both sterilization via the release of Ag + and antiadhesion due to its slippery properties. Following a 7-day cocultivation period with PAO1 bacteria, the coating retained 100 % bactericidal activity and 99.8 % resistance to bacterial adhesion. Moreover, the antialgal efficacy of the AP-TA 0.2 -Ag 1 @Oil coating against Chlorella and P. tricornutum increased by 99.9 % and 99.7 %, respectively. Furthermore, the combination of Ag(Ӏ)-imine coordination bonds and silicone oil effectively preserves the corrosion resistance of the coating. The EIS results demonstrated that the | Z | 0.01 Hz value of the slippery organogel coating was maintained at 1.07 × 10 7  Ω·cm 2 after immersion in 3.5 wt% NaCl solution for 14 days, suggesting excellent anticorrosion performance of the coating. This study provides a novel perspective for the development of marine protective coatings that possess antifouling, self-healing, and anticorrosive properties.

CAS / MDL: 63148-62-9
研究领域: 材料科学 · 海洋防护 · 高分子化学 · 表面工程 · 腐蚀科学 · 生物材料
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JOURNAL OF ALLOYS AND COMPOUNDS · 2018 · IF 3.779

Constructing excellent electromagnetic wave absorber with dielectric-dielectric media based on 3D reduced graphene and Ag(I)-Schiff base coordination compounds

Yanfang Xu,Jinhuan Li,Huanmin Ji,Xuexue Zou,Jiaojiao Zhang,Yi Yan

The dielectric-dielectric composite (SRGA) for electromagnetic absorber was fabricated via integrating Ag(I)-Schiff base coordination compounds (SSBCC) with three-dimensional reduced graphene aerogel (3D-rGA) powders. SRGA showed excellent electromagnetic wave absorption properties in terms of reflection loss, absorption band width and absorber thickness. Specially, when the mass ratio of SSBC to 3D-rGA powders was 1:3 (SRGA-25), the maximum value of reflection loss at 2 mm was up to −63.82 dB and the effective frequency bandwidth of 6.28 GHz (10.16–16.44 GHz) at 2.5 mm can be obtained. The mechanism investigation of electromagnetic wave absorption for SRGA showed that the enhanced electromagnetic wave absorption was ascribed to enhanced polarization loss derived from good 3D-conductive-network units of 3D-rGA, abundant interfaces caused by the media heterostructure due to the introduction of SSBCC and the good impedance matching condition. And 3D-rGA based materials might be put into practical application only in powder state due to the very low strength of the buck state. Therefore, the investigation on SRGA in our contribution is considered to be an actual performance evaluation of the materials based on three-dimensional graphene for microwave attenuation. This work also provided a method for fabricating excellent graphene-based electromagnetic wave absorbers by simply mixing a suitable dielectric lossy material, e.g. SSBCC.

研究领域: 材料科学 · 电磁学 · 纳米技术
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MICROCHIMICA ACTA · 2018 ·Vol. 185 ·期 11 ·1-10 · IF 5.705

Green emitting N,S-co-doped carbon dots for sensitive fluorometric determination of Fe(III) and Ag(I) ions, and as a solvatochromic probe

Zhu Xiang,Wang Jianying,Zhu Yuhua,Jiang Honghao,Tan Di,Xu Ziqiang,Mei Tao,Li Jinhua,Xue Longjian,Wang Xianbao

N,S-co-doped carbon dots (N,S-CDs) were synthesized via a single-step solvothermal process by using sodium lignosulfonate and p-phenylenediamine as carbon/nitrogen/sulfur sources. The N,S-CDs have an average diameter of 2.02 ± 1 nm and display green fluorescence, with excitation/emission peak wavelengths at 380/540 nm for optimal fluorescence. Fluorescence is excitation wavelength-dependent and stable in aqueous salt solutions. The fluorescence of the N,S-CDs is selectively quenched by Fe(III) and Ag(I) ions. These ions can be quantified by fluorometry with a limit of detection of 1.7 μM for Fe(III) ions and 11.6 μM for Ag(I) ions. The N,S-CDs also undergo solvatochromism in that emission is green in water solution but blue in polar organic solvents such as ethanol or N,N-dimethylformamide. The color of fluorescence gradually shifts from green to blue when continuously increasing the fraction of organic solvent in water. N,S-co-doped carbon dots (N,S-CDs) are synthesized by using sodium lignosulfonate and p-phenylenediamine as C/N/S sources. The N,S-CDs can sensitively detect Fe(III) and Ag(I) ions based on fluorometry, and can be used as a solvatochromic probe.

研究领域: 分析化学 · 材料科学 · 环境科学
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TETRAHEDRON · 2019 · IF 2.379

Synergistic Ag(I)/nBu4NBr-catalyzed fixation of CO2 to β-oxopropyl carbonates via propargylic alcohols and monohydric alcohols

Jingyuan Li,Qingwen Song,Hengxuan Zhang,Ping Liu,Kan Zhang,Junwen Wang,Dengsong Zhang

Chemical fixation of carbon dioxide under mild reaction conditions e.g. atmospheric pressure and low temperature depends upon the ability of catalyst. Herein, a synergistic catalytic scheme of silver sulfadiazine/ n Bu 4 NBr was described for the three-component reaction of propargylic alcohols, CO 2 , and monohydric alcohols. This catalytic system was demonstrated effectively to provide β-oxopropyl carbonates in excellent yields (up to 99% yield with 5 mol% catalyst). The method tolerated a wide scope of propargylic alcohols and monohydric alcohols under atmospheric CO 2 pressure and solvent-free conditions. The excellent catalytic performance was attributed to the synergistic catalysis confirmed by the careful experiments.

研究领域: 催化 · 有机化学 · 绿色化学
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ACS Applied Materials & Interfaces · 2021 · IF 9.229

Anchoring Ag(I) into Nitro-Functionalized Metal–Organic Frameworks: Effectively Catalyzing Cycloaddition of CO2 with Propargylic Alcohols under Mild Conditions

Jian Zhao,Zhuo-Hao Jiao,Sheng-Li Hou,Yue Ma,Bin Zhao

Carboxylative cyclization of propargylic alcohols with CO2 is significant in synthetic chemistry, but harsh conditions are often needed according to reported results. Herein, a new stable nitro-functionalized metal–organic framework (MOF) of {[Co3(L)2(bpy)4(H2O)2]·DMF·H2O·bpy}n (1) was fabricated through the solvothermal reaction, which exhibited excellent stability in acid and basic solutions. Owing to the porous structure, unsaturated metal sites, and uncoordinated 4,4′-bpy ligands, 1 can serve as an excellent platform for catalytic applications. Hence, Ag(I) ions were incorporated in 1 through a postsynthetic method, and the as-synthesized Ag-1 catalyst with low metal loading (0.64 mol %) displayed excellent catalytic performance in the chemical fixation of CO2 with alkynols under room temperature and atmospheric pressure. The results of 1H NMR analyses further confirmed that Ag-1 can efficiently activate hydroxyl groups and promote the reaction. Moreover, the turnover frequency (TOF) of the Ag-1 catalyst can reach 262 h–1 in a short period of time, which is a high TOF value among the state-of-the-art MOF-based catalysts for catalyzing cycloaddition of CO2 with propargylic alcohols.

研究领域: 化学 · 材料科学 · 催化领域
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2017 · IF 2.536

Ultrasensitive detection of Ag(I) based on the conformational switching of a multifunctional aptamer probe induced by silver(I)

Yu-Feng Zhu,Yong-Sheng Wang,Bin Zhou,Yan-Qin Huang,Xue-Jiao Li,Si-Han Chen,Xiao-Feng Wang,Xian Tang

We for the first time confirmed that the low concentrations of Ag(I) could induce a silver specific aptamer probe (SAP) from a random coil sequence form to G-quadruplex structure. Thereby, a novel highly sensitive fluorescence strategy for silver(I) assay was established. The designed multifunctional SAP could act as a recognition element for Ag(I) and a signal reporter. The use of such a SAP can ultrasensitively and selectively detect Ag(I), giving a detection limit down to 0.64   nM. This is much lower than those reported by related literatures. This strategy has been applied successfully for the detection of Ag(I) in real samples, further proving its reliability. Taken together, the designed SAP is not only a useful recognition and signal probe for silver, but also gives a platform to study the interaction of monovalent cations with DNA .

研究领域: 分析化学 · 生物化学 · 纳米技术
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RSC Advances · 2016 ·Vol. 6 ·期 73 ·69370-69380 · IF 3.289

Uptake of Fe(III), Ag(I), Ni(II) and Cu(II) by salicylic acid-type chelating resin prepared via surface-initiated atom transfer radical polymerization

Juncai Zhang,Youning Chen

With chloromethylated polystyrene resin being the base material, a new type of salicylic acid-type chelating resin with high capacity was prepared by grafting glycidyl methacrylate (GMA) on the surface of the resin via surface-initiated atom transfer radical polymerization and followed by the derivatization with 5-aminosalicylic acid. Fourier-transform infrared spectrometry and X-ray photoelectron spectroscopy were used to characterize the surface composition of the resin. It was found that the grafting degree of GMA increased linearly with the extension of ATRP time and GMA concentration. The maximum adsorption capacities of the resin were up to 4.23 mmol g−1 for Fe(III), 4.02 mmol g−1 for Ag(I), 2.36 mmol g−1 for Ni(II) and 1.75 mmol g−1 for Cu(II) at pH 4.0, respectively. The adsorption kinetics of the four metal ions conform to the model of pseudo second-order kinetics, and adsorption equilibria were better characterized by the Langmuir equation. Thermodynamic parameters were calculated to understand the nature of the adsorption process. The resin possesses excellent desorption rate and reusability. All these results indicate that the resin could be potentially applied to the efficient removal of heavy metal ions from waste water.

CAS / MDL: 89-57-6 106-91-2
研究领域: 环境科学 · 材料科学
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AICHE JOURNAL · 2016 ·Vol. 62 ·期 5 ·1740-1746 · IF 2.98

Efficient adsorptive desulfurization by task-specific porous organic polymers

Tian Jin,Shuhao An,Xuejing Yang,Jun Hu,Hualin Wang,Honglai Liu,Ziqi Tian,De-en Jiang,Nada Mehio,Xiang Zhu

A task-specific mesoporous organic polymer (TSPOP) with unique features like good porosity and rich aromatic phenyl groups was facilely made and utilized as a promising adsorptive desulfurization absorbent for the first time. The material exhibits an efficient saturated adsorption of dibenzothiophene (DBT), as high as 111.1 mg g −1 . In addition, the intrinsic mesoporous skeleton of TSPOP gave rise to a facile incorporation of uniform Ag(I) species inside the network which facilitated the uptake of organosulfur compounds. A significantly higher saturated DBT adsorption for Ag(I)-loaded TSPOP reaches 203.7 mg g −1 via a multiple-site interaction. A detailed model study based on the density functional calculation provides a deeper understanding of the origin of this high activity. In addition to the π–π stacking between DBT and phenyl rings, there exists an additional π-complexation adsorption with Ag(I) ions, thus, significantly improving the DBT capture performance. © 2016 American Institute of Chemical Engineers AIChE J , 62: 1740–1746, 2016

CAS / MDL: 110-02-1
研究领域: 化学工程 · 材料科学
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MATERIALS CHEMISTRY AND PHYSICS · 2023 · IF 4.6

3D magnetic MXene as promising adsorbent materials for Ag(I) removal

Wenjuan Zhang,Yuheng Li,Yaxian Wang,Youliang Wang,Miao Kou,Xiangyue Yang,Qianqian Chu,Kun Zhao

An efficient route is proposed to synthesize a novel three-dimensional (3D) magnetic MXene aerogel (3D MXene/Fe 3 O 4 ). 3D MXene were synthesized by self-assembly of 2D MXene Ti 3 C 2 T x using ethylenediamine (EDA) as crosslinking inducer, then Fe 3 O 4 was in situ coprecipitation onto 3D MXene. 3D MXene/Fe 3 O 4 was applied as an adsorbent for Ag(I) removal from aqueous solutions. 3D MXene/Fe 3 O 4 exhibits a cross-linked 3D porous network with magnetic Fe 3 O 4 nanoparticles uniformly dispersed on its surface and edges. The maximum adsorption capacity of 3D MXene/Fe 3 O 4 for Ag(I) was 2385 mg g −1 . The kinetics and isothermal process during adsorption were described accurately by the pseudo-second-order model and the Freundlich isotherm model, and the adsorption process was driven by chemisorption and multilayer adsorption, where the diffusion mechanism involved surface diffusion and intraparticle diffusion. Furthermore, the 3D MXene/Fe 3 O 4 are recyclable, retaining 71% of the initial removal rate after 5 adsorption/desorption cycles.

CAS / MDL: 7789-24-4
研究领域: 环境科学 · 材料科学
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