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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2021 · IF 6.953

Selenium-agarose hybrid hydrogel as a recyclable natural substrate for selenium-enriched cultivation of mung bean sprouts

Lu Cao,Jian Zhu,Na Li

Selenium (Se) is an essential trace element for human beings and animals. Traditional plant Se enrichment technology suffers from selenium pollution. Herein, environmentally friendly Se-agarose (Se-Agar) hybrid hydrogels are prepared by simply mixing agar with different Se species including selenocarrageenan (SeCA), selenite and Se yeast under heating and stirring for 0.5 h without any other reagent. Such Se-Agar hybrid hydrogels with excellent biocompatibility were used as natural substrates for the cultivation of Se-enriched mung bean sprouts. Compared with Se yeast, SeCA and selenite show a better Se enrichment effect on mung bean sprouts. Furthermore, the growth indices including plant weight and plant height of mung bean sprouts were investigated with different concentrations and sources of Se. Notably, the Se-Agar hybrid hydrogels could be easily regenerated and reused for multiple cycles. The results indicated that Se-Agar hybrid hydrogels as recyclable natural substrates offer a simple, sustainable and affordable strategy for plant Se enrichment.

研究领域: 植物学 · 环境科学 · 食品科学
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Methods and Applications in Fluorescence · 2019 ·Vol. 8 ·期 1 ·015002 · IF 2.94

Novel fluorescein- and pyridine-conjugated schiff base probes for the recyclable real-time determination of Ce3+ and F−

Fanyong Yan,Yingxia Jiang,Keqing Fan,Tengchuang Ma,Liang Chen,Cong Ma

The effect of aminopyridines substituted at different positions on the fluorescence properties deserves to be studied. Since 2-aminopyridyl-based probes have been reported, the effects of 3-aminopyridine and 4-aminopyridine on the performance of fluorescein probes were discussed in here. Two Schiff base fluorescein probes FN-1, FN-2 were designed and synthesized. Among them, since the ligand shows a highly selective and sensitive response to metal charge transfer (LMCT), the fluorescence of FN-1 can be quenched by Ce3+ ions in PBS buffer. At the same time, a specific precipitation reaction between Ce3+ and F− releases the free probe to restore the fluorescence of FN-1. Therefore, FN-1 can be used for the recyclable 'ON-OFF-ON' detection of Ce3+and F−. The detection limits for Ce3+and F− are 4.48 μM and 11.58 μM in concentration range of 0–50 μM and 0–150 μM. However, due to the para position of N and amino groups on 4-aminopyridine, the spatial structure of FN-2 cannot be complexed with ions, resulting in poor selectivity. Polyvinylidene fluoride (PVDF) membrane containing FN-1 were prepared for the real-time qualitative detection of Ce3+and F− in real water samples. FN-1 exhibits high water solubility and biocompatibility and has been successfully applied to biological imaging in vascular smooth muscle cells (VSMCs).

研究领域: 分析化学 · 生物化学
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Materials · 2023 ·Vol. 16 ·期 4 ·1604 · IF 3.4

High-Strength, Degradable and Recyclable Epoxy Resin Based on Imine Bonds for Its Carbon-Fiber-Reinforced Composites

Yue Jiang,Shuai Wang,Weifu Dong,Tatsuo Kaneko,Mingqing Chen,Dongjian Shi

Carbon fiber (CF) is widely used in the preparation of carbon-fiber-reinforced polymer composites (CFRP) in which it is combined with epoxy resin due to its good mechanical properties. Thermosetting bisphenol A epoxy resin, as one of the most common polymer materials, is a non-renewable resource, leading to a heavy environmental burden and resource waste. To solve the above problems and achieve high mechanical and thermal properties comparable to those of bisphenol A, herein, a high-performance, degradable and recyclable bio-based epoxy resin was developed by reacting the lignin derivative vanillin with 4-amino cyclohexanol via Schiff base. This bio-based epoxy resin showed a Young’s modulus of 2.68 GPa and tensile strength of 44 MPa, 36.8% and 15.8% higher than those of bisphenol A epoxy, respectively. Based on the reversible exchange reaction of the imine bond, the resin exhibited good degradation in an acidic environment and was recoverable by heat treatment. Moreover, the prepared epoxy resin could be used to prepare carbon fiber (CF)-reinforced composites. By washing off the epoxy resin, the carbon fiber could be completely recycled. The recovered carbon fiber was well preserved and could be used again for the preparation of composite materials to realize the complete recovery and utilization of carbon fiber. This study opens a way for the preparation of high-performance epoxy resin and the effective recycling of carbon fiber.Keywords:epoxy resin;degradable;recycled;bio-based

研究领域: 材料科学 · 环境科学
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Nanomaterials · 2023 ·Vol. 13 ·期 6 ·966 · IF 5.3

Recyclable Magnesium-Modified Biochar Beads for Efficient Removal of Phosphate from Wastewater

Biao Hu,Nina Yan,Zhiyu Zheng,Lei Xu,Hongde Xie,Jingwen Chen

Although ball milling is effective for biochar modification with metal oxides for efficient phosphate removal, the recyclability of the adsorbent as well as the precursors for modification, still need to be optimized. Herein, a magnesium-modified biochar was first prepared with the precursor of MgCl2·6H2O through the solvent-free ball milling method. After that, recyclable biochar beads were fabricated with the introduction of sodium alginate and Fe3O4.The beads were proved to have excellent adsorption performance for phosphate with a saturated capacity of 53.2 mg g−1, which is over 12 times higher than that of pristine biochar beads. Although the particle size reduction, surface area, and O-containing group increments after milling are beneficial for adsorption, the remarkable promotion in performance should mainly result from the appropriate formation of magniferous crystals on biochar, which greatly accelerates the electrostatic interactions as well as precipitation for adsorption. The beads also exhibited excellent magnetism-driven recyclability, which greatly avoids secondary contamination and broadens the application field of the adsorbent.Keywords:biochar;modification;adsorption;phosphate;sodium alginate;recyclable

CAS / MDL: 50-81-7 1317-61-9
研究领域: 环境科学 · 废水处理 · 材料科学 · 化学工程
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Journal of Environmental Chemical Engineering · 2024 · IF 7.4

Fabrication of TiO2-enriched MXene microfibers to give efficient and recyclable photocatalysts for sustainable wastewater treatment

Peng Wang,Chengming Yu,Jiale Huang,Zhudan Jiang,Xinyu Jiang,Shanglin Xiang,Dongyu Cai

Developing an efficient photocatalyst with good recyclability is vital for the sustainability and affordability of photocatalytic technology in the treatment of wastewater. This work demonstrates a facile route for realizing robust TiO 2 @Ti 3 C 2 T x fibers with exceptional photocatalytic capability and recyclability. In this route, an alkalization/de-alkalization process was developed to treat a concentrated Ti 3 C 2 T x suspension known as MXene sediment, followed by a wet spinning process. The pretreatment of Ti 3 C 2 T x suspensions promoted the expansion of the d-spacing of stacked Ti 3 C 2 T x layers in the microfibers. It was found that this was beneficial for increasing the population of TiO 2 nanoparticles grown from Ti 3 C 2 T x layers. The calcination of these fibers was systematically investigated to optimize the photocatalytic performance of TiO 2 @Ti 3 C 2 T x fibers. Thanks to the TiO 2 nanoparticles, the resulting fibrous photocatalysts not only enabled the fast degradation of RhB dyes but also exhibited excellent recoverability from water.

研究领域: 材料科学 · 环境科学
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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

High-performance easy-degradable and recyclable thermosetting polyurethanes via dynamic cross-linking and abundant hydrogen bonding for foam sensor applications

Hongrui Liang,Yifen Xu,Jing Song,Yongxi Cui,Yubo Chen,Yu Cao,Qinglong An,Lixian Yin,Tongan Bu,Zhi Wang

Developing degradable and recyclable thermosetting polyurethanes represents a significant step toward environmental protection and resource conservation. However, achieving these properties often compromises mechanical performance and thermal stability. To address this challenge, we developed a high-performance degradable and recyclable thermosetting polyurethane (IP-AD-BA1) by integrating dynamic cross-linkers with abundant hydrogen bonding. First, a polyurethane prepolymer was synthesized using adipic dihydrazide (AD), a chain extender enriched with hydrogen bond donors and acceptors, to generate abundant hydrogen bonding within the polyurethane structure. This prepolymer was then cross-linked to form IP-AD-BA1 using boric acid as the dynamic cross-linker. Comparisons with other polyurethanes of the same type reveal that IP-AD-BA1 exhibits excellent comprehensive performance. This includes outstanding mechanical properties (tensile strength of 51.1 MPa and toughness of 152.1 MJ m −3 ), as well as thermal stability (5% weight loss temperature of 322.5 °C). Moreover, IP-AD-BA1 offers rapid recyclability under mild conditions (110 °C, 15 MPa) while maintaining its mechanical and thermal properties after recycling. It can also be degraded in ethanol, enabling recovery as a linear polyurethane oligomer. Finally, we utilized IP-AD-BA1 to fabricate recyclable foam sensors capable of effectively detecting strain and stress, thereby broadening the potential applications of thermosetting polyurethanes.

研究领域: 材料科学 · 环境科学
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Journal of Environmental Sciences · 2017 · IF 2.865

Alkynyl carbon materials as novel and efficient sorbents for the adsorption of mercury(II) from wastewater

Yingjie Li,Wenfeng Li,Qingnan Liu,Hong Meng,Yingzhou Lu,Chunxi Li

For the first time, a series of alkynyl carbon materials (ACMs) were prepared via the mechanochemical reaction of CaC 2 with six polyhalogenated precursors, namely CCl 4 , C 2 Cl 6 , C 2 Cl 4 , C 6 Cl 6 , C 6 Br 6 , and C 14 H 4 Br 10 (ACM-1, ACM-2, ACM-3, ACM-4, ACM-5, and ACM-6, respectively) and used for the adsorptive removal of mercury from aqueous solutions. Based on preliminary investigations, the adsorption of mercury on ACM-5 was studied in depth. Specifically, the effect of pH on mercury adsorptivity , adsorption kinetics, thermodynamics, isotherms, and recyclability was studied. The adsorptivity of mercury on ACMs was found to be closely related to the hydrocarbon precursor, specific surface area of sorbent , and the alkynyl content. ACM-5 showed the best performance and is among the best raw carbonaceous sorbents reported so far, with a Langmuir saturated adsorption capacity of 191.9   mg   g −   1 . The promising mercury adsorption performance mainly arises from the strong Lewis soft acid–soft base interactions between the alkynyl groups and mercury ions. The adsorption isotherms could be satisfactorily correlated with the Langmuir equation. The results show that the ACMs can be used as efficient sorbents for the removal of mercury and may also be useful for the adsorption of other heavy metals.

CAS / MDL: 84852-53-9 87-82-1
研究领域: 环境科学 · 材料科学
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2025 · IF 8.5

Cellulose-enhanced MoS2 bifunctional hydrogel for efficient methylene blue degradation, human body sensing, and recyclability

Junzheng Chen,Xikun Zhang,Xue Lv,Shurui Yi,Di Fang

In this study, the dispersion behavior of MoS₂ in ionic liquids (ILs) with varying alkyl chain lengths was the primary focus of investigation, followed by the design of a novel PAM/SMA/CMC/PDA@MoS 2 hydrogel. By optimizing the concentrations of CMC and PDA@MoS 2 , a bifunctional hydrogel with both sensing and catalytic functions was successfully developed. Mechanical tests revealed that the PAM/SMA/CMC 0.06 /0.09PDA@MoS 2 hydrogel exhibited exceptional mechanical properties, with stress (505.24 kPa), strain (2333.34 %), elastic modulus (20.17 kPa), and toughness (3990.97 kJ/m 3 ). Furthermore, the hydrogel demonstrated superior sensing performance, characterized by high sensitivity (GF = 7.67) and a rapid response time (148 ms) across a wide strain range. These properties enable precise monitoring of physiological movements, coupled with long-term cyclic stability, positioning it as a versatile material for sensors and electrodes. Subsequently, in situ stabilized silver nanoparticles (Ag NPs) were used as a template for the catalytic degradation of methylene blue (MB) using discarded human motion monitoring hydrogels. The degradation followed first-order kinetics (k = 0.54 min −1 at 25 °C) with 85 % efficiency sustained over 10 cycles, demonstrating significant stability and recyclability. This strategy integrates sensor recycling with Ag NPs based dye degradation, addressing environmental concerns and highlighting its potential in sustainable applications.

研究领域: 材料科学 · 环境科学 · 生物医学工程
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POLYMER · 2025 · IF 4.5

Spider silk-inspired tough and recyclable polyurethane with supercold tolerance

Bowen Tan,Liming Tao,Shoubing Chen,Zenghui Yang,Qihua Wang,Lihe Guo,Zhangzhang Tang,Rui Yang,Qian Dou,Xinrui Zhang,Yuqi Li,Tingmei Wang

Developing polyurethane that can withstand ultra-low temperatures is key to expanding its applications in low-temperature environments. Spider silk demonstrates high toughness in low-temperature environments due to its hierarchical hydrogen bonds network. Inspired by spider silk, a polyurethane elastomer (SPU-DTP x ) with exceptional strength, superior toughness, low-temperature resistance, and recyclability were synthesized. The dense hydrogen bonds in the urethane bonds lead to curled and entangled molecular chains at low temperature. SPU-DTP 0.8 achieves a maximum tensile strength of 86.71 MPa, maximum elongation at break reaching 226.93 % at −90 °C, with toughness of SPU-DTP 0.8 of 109.98 MJ m −3 , only 37.27 % lower than that at 20 °C. Utilizing hydrogen bonds and molecular chain migration, SPU-DTP 0.8 demonstrates excellent recyclability, maintaining key mechanical properties after reprocessing. This elastomer could endure extreme supercold temperatures and offer considerable promise for creating elastic devices, flexible spacecraft, and soft robots designed for use in extremely low-temperature environments like outer space or polar areas.

CAS / MDL: 25190-06-1
研究领域: 材料科学 · 生物仿生学
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COMPOSITES PART B-ENGINEERING · 2018 · IF 4.92

Preparation of chitin fastening Ag@AgCl composite film with decontamination properties by one step coagulation method

Chunwang Yi,Jingkai Liu,Deqian Meng,Jing Lv,Xiaomin Zhang,You shu,Shengpei Su,Jin Zhu

A chitin-fastening Ag@AgCl composite film with decontamination properties was successfully prepared by one-step coagulation method of the chitin- LiCl/Dimethyl Acetamide (DMAc) solution with AgNO 3 . In this process, AgCl was formed in a chitin solution with the addition of AgNO 3 solution, and with the help of excess Cl − a solution of AgCl was formed. AgCl nanocrystals embedded on the surface of chitin were obtained after the solution was put into coagulation bath . The AgCl nano-crystals embedded on the surface of chitin film could be partly transformed into the Ag@AgCl by appropriate visible-light irradiation in the air. In order to explore the morphology and the formation mechanism of the composites, the well-prepared films were characterized by scanning electron microscopy (SEM), X-ray powder diffraction (XRD), Fourier transformation infrared spectroscopy (FTIR), X-ray photo-electron spectroscopy (XPS), thermogravimetric analysis (TGA), ultraviolet spectro-photometry and UV–visible absorption spectrum . The decontamination ability and recyclability of composite film was evaluated by the degradation rate of methyl orange (MO) in recycling process. By comparison, the Ag@AgCl fastened in chitin matrix was more stable than fastened by cellulose matrix. Its photo-degradation efficiency could be still retained up to 95% after 5-cycle testing. Meanwhile, the composite film could be also kept excellent mechanical properties. This work provided a simple pathway to construct the functional chitin film which could be applied as a kind of stable recycling decontamination materials.

研究领域: 材料科学 · 环境科学 · 生物化学
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CHEMOSPHERE · 2020 · IF 5.778

E. coli@UiO-67 composites as a recyclable adsorbent for bisphenol A removal

Yuqiang Xiang,Huaduo Yan,Bingjie Zheng,Aroosha Faheem,Wenli Chen,Yonggang Hu

E. coli @UiO-67 composites were obtained using an effective and simple self-assembly method. The composites showed unique properties as a remarkable and recyclable adsorbent for the efficient removal of bisphenol A (BPA) from water with a high adsorption capacity (402.930 mg g −1 ). The increase in pore size is a key factor why E. coli @UiO-67 composites maintained high capacity. The reason might be due to that the composites with large pore sizes and defects could effectively improve mass transport and active molecular metal sites. The adsorption of BPA is a chemisorption process due to the Zr–OH groups in UiO-67 exhibit affinity toward BPA molecules, π–π interaction, and electrostatic attraction. The adsorption efficiency remained at 82.5% after 15 cycles without any remarkable changes in the PXRD patterns of E. coli @UiO-67. Moreover, the use of microorganism-loading MOFs could reduce the cost to at least 50% and minimize secondary pollution through nanoscale MOFs usage reduction. The developed composites have advantages, including low-cost, high adsorption capacity, easy to be separated and regenerated from aqueous solution, a large number of cycles, short adsorption equilibrium time, and stability, showing excellent application prospects. The presented strategy would be a potentially promising way to produce novel MOFs-based adsorbents with high-performance to control environmental pollution from wastewater.

CAS / MDL: 787-70-2 10026-11-6
研究领域: 环境科学 · 材料科学 · 生物工程
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JOURNAL OF MATERIALS SCIENCE · 2019 ·Vol. 55 ·期 4 ·1854-1864 · IF 3.442

Triazine-based covalent organic polycalix[4]arenes for highly efficient and reversible iodine capture in water

Zhang Zhizhong,Li Liang,An Duo,Li Hanxue,Zhang Xinghua

Novel triazine-based covalent organic polycalix[4]arenes, CalCOPs, were synthesized via the copolymerization of calix[4]arene derivatives and 2,4,6-trichloro-1,3,5-triazine (TCT) or 2,4-dichloro-1,3,5-triazine (DCT). The resulting CalCOPs have permanent pores that can be regulated by the variation of the alkyl chain lengths of the calixarene backbones and the reaction sites. With the alkyl chain length at the low rim in calixarene units increasing from ethyl to butyl during the reaction, the Brunauer–Emmett–Teller surface areas decrease with surface areas of 280, 31.5, 18.4 and 1.6 m 2  g −1 obtained for CalCOP1, CalCOP2, CalCOP3 and CalCOP4, respectively. Among these CalCOPs, CalCOP1 shows ultrahigh absorption for iodine capture in a water solution with an uptake of up to 232 wt%. Furthermore, the adsorption and release efficiency of iodine were obtained by using the UV–Vis spectroscopy. In addition, these polymers can be recycled at least five times while maintaining high removal capacity, suggesting that CalCOPs are ideal absorbent materials for reversible iodine capture in the mitigation of environmental issues.

研究领域: 材料科学 · 环境科学
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