NEW JOURNAL OF CHEMISTRY
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2019
·Vol. 43
·期 20
·7770-7777
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IF 3.069
Shi-Wen Lv,Jing-Min Liu,Chun-Yang Li,Hui Ma,Zhi-Hao Wang,Ning Zhao,Shuo Wang
A novel magnetic nanocomposite named Fe3O4@UiO-66-SO3H with a core–shell structure was first synthesized via a feasible step-by-step assembly strategy, and then employed as an adsorbent to remove methylene blue (MB) from aqueous solution. The characterization by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and Fourier transform infrared (FT-IR) spectroscopy proved that the Fe3O4@UiO-66-SO3H core–shell nanocomposite was successfully prepared. And the as-synthesized Fe3O4@UiO-66-SO3H had a strong affinity towards MB and the maximum adsorption capacity was 297.3 mg g−1. The adsorption of MB could be basically completed within 15 min. The kinetic and isotherm studies indicated that adsorption data could be well fitted to the pseudo-second-order model and Langmuir model. Significantly, Fe3O4@UiO-66-SO3H could selectively adsorb MB from a mixed solution due to the charge-selectivity effect and possessed good reusability. The electrostatic interaction and the π–π interaction were assumed to play a vital role in the adsorption process. All in all, the current study provided a promising sorbent for the efficient and selective removal of MB from dye-containing wastewater.
研究领域:
材料科学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2024
·
IF 8.1
Xiaocan Zhang,Jiashu Long,Mengxin Wang,Yiran Liu,Huixiao Ma
Blending metal-organic frameworks to optimize proton transport pathways is one of the strategies to improve the proton conductivity of proton exchange membranes (PEM). In this paper, amino-sulfonic acid bifunctionalized UiO-66 (NUS) by one-pot solvothermal method is synthesized, and sulfonated poly (ether ether ketone)/NUS-X (SPEEK/NUS-X) hybrid membranes are prepared by mixing NUS into SPEEK matrix. Among them, SPEEK/NUS-1.5 has the highest proton conductivity (177.76 mS cm −1 , 70 °C, 100% RH) and maintain a 300 h conductivity stability. And its maximum power density was 423.2 mW cm −2 , exceeding pristine SPEEK by 2.20 times. Compare to the pristine SPEEK membrane, it is interesting to note the disappearance of SAXS scattering peak of SPEEK/NUS-1.5. It is speculated that this phenomenon was caused by the generation of acid-base pairs between –NH 2 and –SO 3 H, and the improved hydrogen bonding network provides more proton transport channels and immobilizes sulfonic acid groups for improved durability. The resultant proton conductivity is stable over 300 h with about 90% retention.
研究领域:
材料科学
·
化学工程
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产品关联
DOI
高影响因子
Frontiers in Chemistry
·
2022
·
IF 5.545
Zhao Kangyu,Xiang Yanping,Sun Xiaoao,Chen Linjiao,Xiao Jiafu,Liu Xianxiang
In this study, a novel sulfonic acid-modified catalyst for MOFs (UIO-66-SO3H) was synthesized using chlorosulfonic acid as a sulfonating reagent and first used as efficient heterogeneous catalysts for the one-pot conversion of fructose into biofuel 5-ethoxymethylfurfural (EMF) in a cosolvent free system. The physicochemical properties of this catalyst were characterized by Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), and powder X-ray diffraction (XRD). The characterization demonstrated that the sulfonic acid group was successfully grafted onto the MOF material and did not cause significant changes to its morphology and structure. Furthermore, the effects of catalyst acid amount, reaction temperature, reaction time, and catalyst dosage on reaction results were investigated. The results showed that the conversion of fructose was 99.7% within 1 h at 140°C, while the EMF yield reached 80.4%. This work provides a viable strategy by application of sulfonic acid-based MOFs for the efficient synthesis of potential liquid fuel EMF from renewable biomass.
研究领域:
化学工程
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催化科学
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可再生能源
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产品关联
DOI
PubMed
高影响因子
FUEL
·
2024
·
IF 6.7
Wenli Zhang,Yijie Zhou,Zhenzhen Wu,Cheng Pan,Qunpeng Cheng,Guozhi Fan
A porous sulfonic acid-functionalized zirconium-based metal–organic framework possessing both Lewis acid and Brønsted acid sites (UiO-66-SO 3 H) was synthesized and tested for the selective conversion of furfural (FUR) to isopropyl levulinate (IPL) through one-pot cascade reaction. UiO-66-SO 3 H exhibited excellent catalytic performance, and the conversion of FUR as well as the yield and selectivity of IPL reached 96.4 %, 86.0 %, and 89.2 %, respectively. UiO-66-SO 3 H could be simply recovered and reused, but the catalytic performance was significantly decreased. The FUR conversion and IPL yield dropped to 73.8 % and 65.1 %, respectively, after 1 cycle, and the reason for the decrease in the catalyst activity were also investigated. It was found that the decrease was mainly caused by the loss of some −SO 3 H groups, and the cyclic performance of UiO-66-SO 3 H could be restored by supplementing a small amount of BDC-SO 3 Na. A plausible mechanism for the selective synthesis of IPL from FUR was proposed, wherein both Lewis acid and Brønsted acid sites played important roles. This work provides guidance for the selective conversion of FUR into IPL, and the high-valued utilization of biomass and its derivatives.
研究领域:
化学工程
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催化科学
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可再生资源利用
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产品关联
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE
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2023
·Vol. 58
·期 7
·3134-3146
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IF 4.5
Luo Qizhao,Li Jingjing,Yun Panfeng,Qian Libing,Zhang Jinshuai,He Chunqing,Hu Xuejiao,Jiang Haifeng
Desalination through reverse osmosis (RO) membrane is one of the most popular ways. However, conventional RO membranes meet a trade-off between salt rejection and water flux which limit their comprehensive performance. In this work, sulfonated zirconium (IV)-carboxylate metal–organic framework (MOF) material UiO-66-SO 3 H was successfully synthesized, and thin-film nanocomposite (TFN) with UiO-66-SO 3 H-incorporated polyamide (PA) layer was fabricated. Angstrom-sized UiO-66-X ion transport channels with different functional groups in TFN membranes change the membrane morphology and chemistry and accelerate the penetration of water molecules while maintaining the high ion screening effect. As a result, compared to the pristine TFC membrane, the optimized TFN-UiO-66-SO 3 H membrane exhibited an increase in water molecules permeability to 347% and still maintained a salt rejection with ~ 94.7% under 2000 ppm NaCl solution with reverse osmosis (RO) mode, leading to a great improvement of intrinsic separation properties. The improved performance was owing to the size exclusion effect and hydrophilic nature of UiO-66-SO 3 H particles. What is more, the additional water migration channels through the incorporated UiO-66-SO 3 H nanoparticles lead to a boosting water permeation and show optimized performance for desalination. Graphical abstract
研究领域:
材料科学
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环境工程
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膜技术
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产品关联
DOI
高影响因子
LANGMUIR
·
2025
·
IF 3.9
Heng Li,Chengzhong Zhang,Yuhang Jiang,Wenwu Ni,Mingshuo Li,Jing Wang
Widespread dye contamination poses a serious threat to humans and aquatic environments. Metal–organic frameworks (MOFs) with abundant reactive groups and high specific surfaces are candidates for the adsorption of dyes. In this study, good growth of UiO-66-SO3H crystals on the surface of nylon-6 fibers was achieved based on the idea of in situ growth. UiO-66-SO3H with a sulfonic acid group was successfully introduced into nylon-6 electrostatic spinning fiber, and the UiO-66-SO3H@nylon-6 membrane with high specific surface area and a three-dimensional mesh structure was obtained, which effectively solved the problems of clogging of the equipment, difficulty in being separated and recovered from the water, the possible secondary pollution of the water environment caused by the powder form of the MOF material, etc. The UiO-66-SO3H@nylon-6 membrane has a good adsorption capacity for rhodamine B (RhB), and the experimental data are consistent with the pseudo-second-order kinetic model and Langmuir model, which shows that the adsorption is a spontaneous heat absorption process. Pore-filling, hydrogen bonding, π–π interactions, and electrostatic attraction induced by –SO3H are the adsorption mechanisms of RhB on this adsorbent. In conclusion, the UiO-66-SO3H@nylon-6 membrane is an adsorbent capable of rapid adsorption of RhB and can be easily separated from water for recovery, regeneration, and utilization. This study may provide ideas for the application of MOFs in the field of pollutant removal.
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
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2024
·
IF 5.9
Chenxi Lu,Bingqing Hu,Liangzhi Li,Xin Ju,Lishi Yan
5-hydroxymethylfurfural (5-HMF) is a key platform chemical that can be applied to generate varied value-added products. Herein, the sulfonated zirconium/tin Mixed-Metal metal–organic frameworks (MOFs), Sn/UiO-66-SO 3 H catalysts were employed for catalytic conversion of biomass-derived carbohydrates (glucose, sucrose, maltose, starch, and cellulose) to 5-HMF in green deep eutectic solvents (DESs)-water based biphasic system. The Sn/UiO-66-SO 3 H catalysts were prepared by infiltrating Sn 4+ into the UiO-66-SO 3 H via post-synthesis modification. The synthesized catalysts were characterized by PXRD, SEM, FTIR, N 2 adsorption–desorption analysis, XPS, ICP-OES, NH 3 -TPD and Py-FTIR. The synergistic effect of Zr 4+ and Sn 4+ increased the total acidity and pore size of MOFs, thus promoting the catalytic performance of MOFs towards carbohydrates conversion to 5-HMF. The 24-Sn/UiO-66-SO 3 H with impregnation of Sn 4+ for 24 h presented desired catalytic ability, which resulted in 81.5 % and 41.7 % 5-HMF yields from glucose and cellulose in DES betaine-malic acid–water/MIBK biphasic system, respectively. Moreover, the five-recycling test for 24-Sn/UiO-66-SO 3 H demonstrated excellent reusability of the prepared catalyst. This study offered a novel sulfonated Mixed-Metal strategy on MOFs in DES betaine-malic acid–water based biphasic system for the production of 5-HMF from biomass-derived carbohydrates.
研究领域:
催化
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绿色化学
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材料科学
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生物质转化
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化工工程
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产品关联
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2022
·Vol. 57
·期 4
·2909-2923
·
IF 4.682
Zeng Sen,Hou Yaqi,Zhou Yaming,Zhou Xi,Ye Shefang,Wang Miao,Ren Lei
Protein-bound uremic toxins (PBUTs) are difficult to remove through dialytic procedures, and the accumulation of PBUTs is always associated with adverse symptoms in end-stage kidney disease. Hemoperfusions and novel membranes have been developed for the removal of PBUTs, but still suffer from low efficiency. Herein, we investigated the adsorption performance of three zirconium metal–organic frameworks (Zr-MOFs: UiO-66, UiO-66-SO 3 H, and UiO-66-(COOH) 2 ) for two typical PBUTs (indoxyl sulfate, IS; hippuric acid, HA). We found that Zr-MOFs could adsorb PBUTs efficiently with a capacity of as high as 49.5 mg g −1 for IS and 38.3 mg g −1 for HA, respectively, due to the van der Waals interactions, Coulomb interactions, and π – π interactions. Density functional theory simulations demonstrated that H-bonding on basis of the –SO 3 H and –COOH groups could endow MOFs with better absorptivity. Further, to expand to practical hemodialysis applications, we incorporated Zr-MOFs into a polylactide (PLA) matrix to fabricate MOFs-based mixed matrix membranes (MMMs). The MMMs showed excellent in vitro biocompatibility and high water flux up to 260 L m −2 h −1 . Under static conditions, the MMMs could remove HA and IS with a percentage of 75 and 78% in 4 h, respectively, whereas PLA membrane removed 12% of HA and 13% of IS. Under dynamic conditions, MMMs could remove 57% of IS and 54% of HA in 30 min; by contrast, PLA membrane only removed 2.9% of IS and 2.2% of HA. These MOFs-based MMMs with exceptional absorptivity, high water flux, and good biocompatibility might show great prospects in the foreground for the application of safe and efficient blood purification.
研究领域:
材料科学
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生物医学工程
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肾病学
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产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）