SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Xiaoxia Ye,Zhihong Zheng,Jinwei Zhu,Jie Chen,Jianfei Zhou,Bi Shi
Adsorptive removal of mercury ion from wastewater has become a hot topic due to the toxicity and persistence; acquiring adsorbent materials with high-capacity, rapid-kinetic, super-selective while low-cost features are highly demanded. Herein, based on the full functionality of collagen fiber (CF) from the leather waste, we proposed an innovative synthetic approach through exploiting amino-functionalized ZIF-7 (ZIF-7-NH 2 ) as functional groups to facilely in-situ incorporate with CF, affording low-cost but effective adsorbent materials of CF/ZIF-7-NH 2 composite maximizing both functions of CF and ZIF-7-NH 2 in the Hg(II) capture. Remarkably, it exhibits an ultra-high capacity as high as 909.09 mg g - 1 , fast kinetics that could remove 99.01 % of 200 mg·L -1 within 20 min, and significant selectivity of S Hg/M ( K d Hg / K d M ) as large as 522–1017 over Mg 2+ , K + , Ca 2+ , Cd 2+ , and Mn 2+ . We understand such an impressive adsorption is contributed by the synergistic action between functional groups including on the CF and ZIF-7-NH 2 . This study offers an effective method for removing heavy metal ions, achieving efficient removal of Hg(II) ions for pollution control, and promoting the reuse of waste CF to reduce waste accumulation in various aspects.
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JOURNAL OF APPLIED POLYMER SCIENCE
·
2024
·
IF 2.7
Wei Zhao,Hongjing Liu,Chengpeng Zhang,Yuyang Cao,Yuying Xu,Xueli Liu,Zhen Lu
Metal–organic frame UiO-66-NH 2 was modified by 3-glycidyl ether oxypropyl trimethoxysilane (KH560), and KH560-UiO-66-NH 2 was synthetized and added to Pebax to prepare KH560-UiO-66-NH 2 /Pebax mixed matrix membranes (MMMs). The epoxy group of KH560 had an amine-epoxidation reaction with the NH 2 in UiO-66-NH 2 , which prevented UiO-66-NH 2 from agglutinating in the MMMs. In addition, the N H bond and OH bond of KH560-UiO-66-NH 2 could theoretically form hydrogen bonds with CO and N H bonds in the main chain of polymerization, respectively, so as to improve the interfacial compatibility between fillers and polymers. The structure and properties of the filler particles and MMMs were evaluated by Fourier transform infrared spectrometer, x-ray diffraction, scanning electron microscopy, and thermogravimetric analyzer. The results showed that the filler particles were successfully synthesized, and had good crystallinity, uniform size distribution, and good thermal stability. The inorganic and organic interfaces of MMMs had no obvious interface defects. The obtained KH560-UiO-66-NH 2 /Pebax MMMs showed CO 2 permeability of 111.52 Barre and CO 2 /N 2 selectivity of 92.16, which were 85.65% and 88.73% higher than that of pristine membranes, respectively. The gas separation performance of MMMs was significantly improved, exceeding the upper bound of 2008 Robeson.
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Energy Technology
·
2025
·
IF 3.6
Ming Yan,Haoyu Chen,Yu Zhu,Yuxiao Deng,Zhuanlong Yan,Ziyi Lu,Yanlin Chen
In this study, NH 2 –SiO 2 @Ti 3 C 2 T x core–shell microspheres with different Ti 3 C 2 T x contents are prepared by coating Ti 3 C 2 T x nanosheets on the surfaces of SiO 2 microspheres using an electrostatic self-assembly method. The structures, elemental compositions, and microscopic morphologies of NH 2 –SiO 2 @Ti 3 C 2 T x microspheres are investigated by X-Ray diffraction, Fourier-transform infrared spectroscopy, field-emission scanning electron microscopy, and X-Ray photoelectron spectroscopy. The results show that Ti 3 C 2 T x nanosheets are uniformly coated on the surfaces of the SiO 2 microspheres, and the surfaces of the SiO 2 microspheres are modified by NH 2 . The maximum specific surface area of NH 2 –SiO 2 @Ti 3 C 2 T x composite doped with 15 wt% Ti 3 C 2 T x is 29.937 m 2 g −1 , with an average pore size of 0.11848 cm 3 g −1 . The electrochemical performance test results show that after 100 cycles at a C rate of 0.2C, the specific capacity of the NH 2 –SiO 2 @Ti 3 C 2 T x anode material increases by 270.1% compared to that of SiO 2 , reaching 142.5 mAh g −1 . Compared with SiO 2 , the NH 2 –SiO 2 @Ti 3 C 2 T x materials have higher electrical conductivities and Li ion diffusion rates, thereby improving their rate performances, and the discharge specific capacities and cycling stability are superior to those of the SiO 2 anode material.
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STAR Protocols
·
2023
·
IF 0
Shuchao Jiang,Jikai Sun,Guoqing Ren,Weiqiao Deng
Summary CO 2 capture and utilization into liquid fuels and high-added-value chemicals has been regarded as an attractive strategy to mitigate excessive carbon emissions. Here, we present a protocol to capture and convert CO 2 into pure formic acid (HCOOH) solution and solid fertilizer (NH 4 H 2 PO 4 ). We describe steps for synthesis of an IRMOF3-derived carbon-supported PdAu heterogeneous catalyst (PdAu/CN-NH 2 ), which can efficiently catalyze (NH 4 ) 2 CO 3 -captured CO 2 into formate under ambient conditions. For complete details on the use and execution of this protocol, please refer to Jiang et al. (2023). 1
研究领域:
环境科学
·
化学工程
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DOI
PubMed
MICROCHIMICA ACTA
·
2019
·Vol. 186
·期 11
·1-8
·
IF 5.479
Guo Lan,Liu Yuan,Qu Fengli,Liu Zhe,Kong Rongmei,Chen Guang,Fan Wenjing,Xia Lian
A luminescent metal organic framework (LMOF) of type UiO-66-NH 2 was chosen for specific and sensitive detection of trace levels of hypochlorite. Hypochlorite causes the quenching of the blue fluorescence of nano-UiO-66-NH 2 (with excitation/emission maxima at 325/430 nm), and this finding forms the basis for a fluorometric assay for hypochlorite. The method overcomes disadvantages of conventional redox-probes which are interfered by oxidants with oxidation capability stronger than that of hypochlorite. Compared with other fluorescent probes for sensing hypochlorite, UiO-66-NH 2 has a comparable detection limit of 0.3 μmol L −1 and a broad linearity relationship in the range of 1–8 μmol L −1 . The probe was successfully applied to the detection of hypochlorite in complex water samples and living Hela cells.
Schematic representation of hypochlorite induced quenching of the blue fluorescence of nano-UiO-66-NH 2 (with excitation/emission maxima at 325/430 nm) through energy transfer. It overcomes disadvantages of conventional redox-probes which are interfered by oxidants with oxidation capability stronger than that of hypochlorite.
研究领域:
分析化学
·
材料科学
·
生物医学
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DOI
高影响因子
MICROCHIMICA ACTA
·
2021
·Vol. 188
·期 6
·1-11
·
IF 5.833
Ma Mingxuan,Zhang Jian,Li Peipei,Du Yingxiang,Gan Jie,Yang Jiangxia,Zhang Liu
Metal-organic framework (UiO-66-NH 2 )-incorporated organic polymer monolith was prepared by thermal polymerization. By virtue of the superior physical and chemical properties, the UiO-66-NH 2 -modified organic monolith was then functionalized by chiral selector cellulase via the condensation reaction between the primary amino groups and aldehyde groups. The synthesized materials were characterized by Fourier transform infrared spectroscopy, high-resolution transmission electron microscopy, scanning electron microscopy, X-ray photoelectron spectrometry, thermogravimetric analysis, and nitrogen sorption isotherm. The cellulase@poly(glycidyl methacrylate-UiO-66-NH 2 -ethylene glycol dimethacrylate) (cellulase@poly(GMA-UiO-66-NH 2 -EDMA)) monolith was applied to enantiomerically separate the basic racemic forms of metoprolol, atenolol, esmolol, bisoprolol, and propranolol. In contrast to the cellulase@poly(GMA-co-EDMA) monolith without UiO-66-NH 2 , the cellulase@poly(GMA-UiO-66-NH 2 -EDMA) monolith reveals significantly improved enantiodiscrimination performance for metoprolol (Rs: 0 → 1.67), atenolol (Rs: 0 → 1.50), esmolol (Rs: 0 → 1.52), bisoprolol (Rs: 0 → 0.36), and propranolol (Rs: 0 → 0.44). The immobilization pH of cellulase, buffer pH, UiO-66-NH 2 concentration, and the proportion of organic modifier were evaluated in detail with enantiomerically separating chiral molecules. The intra-day, inter-day, column-to-column, and inter-batch precision have been discussed, the result was preferable, and the relative standard deviation (RSD) of separation parameters was <4.3%. Graphical abstract
Schematic representation of the preparation of a UiO-66-NH 2 -modified organic polymer monolith for enantioseparating five racemic β-blockers. UiO-66-NH 2 was synthesized and converted into a monolith as the stationary phase. Then, the modified monolith containing cellulase as the chiral selector was applied in a capillary electrochromatography system for enantioseparating chiral drugs.
研究领域:
分析化学
·
药物化学
·
生物技术
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DOI
PubMed
高影响因子
ADSORPTION SCIENCE & TECHNOLOGY
·
2016
·
IF 0.633
Jing-Hua Yang,Xiao-Mao Zhou,Yu-Ping Zhang,Jun Chen,Hai-Weng Ma
In this paper, a novel polymerized fiber doped with metal–organic frameworks (UIO-66(Zr)-NH2) was developed in a capillary by microwave irradiation. The fiber was successfully prepared using 4-vinyl pyridine as the monomer and ethylene glycol dimethacrylate as the cross-linker to reinforce its durability. The resultant fiber was applied to extract sulfonylurea herbicides from environmental soil and water samples before analysis with high-performance liquid chromatography. The optimization of different parameters affecting solid-phase microextraction procedure was carried out. Under the optimum experimental conditions, the extraction capability of the hybrid fiber was two times greater than that of the polymer fiber without UIO-66(Zr)-NH2.The proposed hybrid fiber extraction method exhibited low detection limits (0.19–1.79 µg/l), good precision (<12.0%), and wide linear range (10–700 µg/l). Satisfactory recoveries of sulfonylurea herbicides were obtained with spiked soil and water samples in the range of 75.7–94.2 and 82.2–95.3%, respectively.
研究领域:
分析化学
·
环境科学
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DOI
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CHEMICAL ENGINEERING JOURNAL
·
2020
·
IF 10.652
Feng Zhao,Weixia Yang,Yong Han,Xueli Luo,Wenzhi Tang,Tianli Yue,Zhonghong Li
The transformation of metal-organic frameworks (MOFs) to metal-organic gels (MOGs) is an attractive but challenging issue because they are generally regarded as the opposite, with the former being hard and the latter soft. Herein, a straightforward strategy was developed to synthesize amorphous Zr-MOG-12 by gelatinization of UiO-66-NH 2 (i.e. Zr-MOF) via a facile standing time-controlled crystallization method. The precursor ZrCl 4 obtains oxide and hydroxide bridges after standing at room temperature, which promotes the formation of [Zr 6 O 4 (OH) 4 ] 12+ clusters and induces rapid and excessive nucleation rate, and further leads to the coordination perturbation of UiO-66-NH 2 nanoparticles to achieve Zr-MOG-12. The as-prepared Zr-MOG-12 integrates the more hierarchical porous structure of gel-based soft materials and the amorphous structure of lower-coordinated active sites, which exhibits superb adsorption capacity for Pb(II) with excellent selectivity and reusability, indicating that Zr-MOG-12 is more promising to removal Pb(II) in practical water treatment . In addition, the transformation of amorphous Zr-MOG-12 to highly crystaline Zr-MOF’ has been achieved by the solvothermal reorganization using glacial acetic acid as the crystallization promoter. The novel methods proposed in this study successfully link crystalline MOF with amorphous MOG, providing new opportunities for facile preparation and transformation of MOFs and MOGs.
研究领域:
材料科学
·
环境科学
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JOURNAL OF HAZARDOUS MATERIALS
·
2019
·
IF 7.65
Peng Liao,Binrui Li,Lin Xie,Xiaoao Bai,Han Qiao,Qianqian Li,Biwei Yang,Chongxuan Liu
Engineered nanoparticles-mediated contaminant transport has been recognized as a significant process governing the mobility of metals and radionuclides in groundwater. Engineered silicate nanoparticles (ESNPs) are attractive materials for the sequestration or extraction of Cr(VI) and other metals and radionuclides from groundwater. While great efforts have been devoted toward the application of these materials for Cr(VI) sequestration, the underlying interface adsorption mechanism is not thoroughly elucidated. This study investigates the immobilization mechanisms of Cr(VI) on a representative ESNPs, NH 2 -MCM-41, over a range of water chemistry conditions. By combining batch adsorption experiments with an array of complementary characterizations, we provided spectroscopic and microscopic evidence that the electrostatic interactions between the positively charged NH 2 -MCM-41 surface derived from amino functionality and the negatively charged Cr(VI) species was the dominant mechanism responsible for Cr(VI) immobilization. In addition, the weak hydrogen bonding interactions may also contribute to adsorption to a degree. Furthermore, thermodynamic studies suggested a favorable, spontaneous, and exothermic adsorption process. Site energy analysis illustrated that the distribution of energy binding sites on NH 2 -MCM-41 is Cr(VI) loading dependent. The new insights provided here can advance understanding of the transport of Cr(VI) associated NH 2 -MCM-41 that benefits the application of ESNPs-based technologies for metals immobilization in groundwater.
研究领域:
环境科学
·
纳米技术
·
污染治理
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PubMed
高影响因子
RSC Advances
·
2016
·Vol. 6
·期 57
·51591-51597
·
IF 3.289
Dongdong Lu,Fangyuan Gai,Zhen-An Qiao,Xue Wang,Tao Wang,Yunling Liu,Qisheng Huo
This work demonstrated that a series of ultrabright fluorescent silica nanoparticles have been synthesized and designed via the reverse microemulsion method to encapsulate (2,2′-bipyridine)2-(5-aminophenanthroline) Ru bis(hexafluorophosphate) (Rubpy-phen). Transmission electron microscopy (TEM), scanning electron microscopy (SEM), dynamic light scattering (DLS), inductively coupled plasma (ICP) and fluorescence spectra were used to study the morphology and properties of the nanoparticles. By introducing ethanol into the reaction system, the obtained uniform fluorescent nanoparticles showed monodispersity and controllable size. With an increase of nanoparticle size (from 50–180 nm), the relative brightness of the nanoparticles was greatly improved from 534 to 86 972 by comparison with free dye molecules. Due to the protection of the silica matrix, the fluorescence of high concentration dye-doped silica nanoparticles (Rubpy-phen NPs) is not quenched, which results in higher fluorescence intensity and relative brightness. Moreover, the silica matrix can also protect Rubpy-phen from leakage. Due to the high brightness and biocompatibility, Rubpy-phen NPs have potential applications in the biological field.
研究领域:
材料科学
·
生物学
·
纳米医学
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高影响因子
INORGANIC CHEMISTRY COMMUNICATIONS
·
2026
·
IF 5.9
Miao Miao,Xue-Rui Dong,Mei-Lin Chen,Tong-Tong Xu,Zhe Lin,Qiao Gao
Quercetin (Qu), a naturally occurring flavonoid, is critically involved in sustaining human physiological health. Therefore, it is imperative to rationally design a proficient electrochemical sensor capable of sensing Qu. Herein, a ternary nanocomposite composed of Keggin-type polyoxometalate (PMo 12 ), carbon nanotubes (CNTs), and zirconium-based MOF (UiO-66-NH 2 ) was successfully fabricated to develop a sensitive electrochemical sensor for Qu determination. Benefiting from the synergistic integration of diverse components, the high conductivity of CNTs, good electrocatalytic performance of PMo 12 , and favorable adsorption capacity of UiO-66-NH 2 jointly facilitated the adsorption and electron transfer process of Qu at the electrode interface. The constructed sensor showed a broad linear detection range of 10–160 μM, high detection sensitivity reaching 0.226 μA·μM −1 , and a detection limit as low as 0.486 μM (S/N = 3) at the optimized working conditions. Besides, the developed sensor exhibited outstanding selectivity, stability, reproducibility, and repeatability. By determining the Qu content in Flos Sophorae Immaturus samples, we further confirmed the actual application capability of the constructed sensor. Satisfactory recoveries of 97.01%–101.08% were obtained, which strongly validated the reliability and accuracy of the proposed electrode for practical Qu analysis.
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INORGANIC CHEMISTRY
·
2026
·
IF 4.7
Hangwei Jia,Yaqi Jin,Junwei Feng,Bailin Chen,Feng Yu,Xueling Hou
Guanidine units have garnered significant attention in the study of ultraviolet (UV) nonlinear optical (NLO) materials due to their excellent microscopic optical properties, making them ideal systems for developing novel optical devices. A novel guanidinium-templated UV NLO crystal, [C(NH2)3]SbCl4 (GSC), was successfully synthesized via an aqueous solution method. GSC crystallizes in the orthorhombic chiral space group P212121, featuring a seesaw shaped [SbCl4]− anion. Remarkably, GSC exhibits a moderate second harmonic generation (SHG) response of 1.1 × KDP at 1064 nm and a large refractive index difference of 0.2 at 546 nm. This NLO effect originates from the synergistic interaction between the [C(NH2)3]+ unit and the stereochemically active [SbCl4]− unit. This work provides a candidate for the guanidine family of NLO materials.
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