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Advanced Science · 2025 · IF 14.1

Construction of a Biomimetic Tubular Scaffold Inspired by Sea Sponge Structure: Sponge-Like Framework and Cell Guidance

Si Meng,Nihuan Wu,Jie Fang,Yidan Yu,Xin Tang,Yihan Wang,Xiaokang Deng,Cheng Qi,Tiantian Kong,Tengda Ding,Zhou Liu

Engineering hollow fibers with precise surface microstructures is challenging; yet, essential for guiding cells alignment and ensuring proper vascular tissue function. Inspired by Euplectella sponges, a novel strategy to engineer biomimetic hollow fibers with spiral surface microstructures is developed. Using oxidized bacterial cellulose, bacterial cellulose, and polydopamine, a “brick-and-mortar” scaffold is created through precise shear control during microfluidic coaxial spinning. The scaffold mimics natural extracellular matrices, providing mechanical stability and supporting cell growth. In vitro studies show successful co-culture of endothelial cells (ECs) and smooth muscle cells (SMCs), with SMCs aligning along spiral surface microstructures and ECs forming a confluent inner layer. In vivo implantation confirms biocompatibility, biodegradability, and low immunogenicity. This Euplectella -inspired scaffold presents a promising approach for vascular tissue engineering and regenerative medicine.

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Nano Research · 2024 · IF 9.5

Coupled Cu doping and Z-scheme heterojunction for synergistically enhanced tetracycline photodegradation

Shen Huidong,Yang Chunming,Hong Song,Hao Leiduan,Xu Liang,Robertson Alex W.,Sun Zhenyu

Semiconductor-based photocatalysis by utilizing solar energy for sustainable organic pollutant elimination has been a promising tactic to alleviate environmental issues. Nevertheless, the development of robust and efficient photocatalysts to degrade organic pollutants still faces major challenges because of insufficient charge separation. Here we design and fabricate a heterojunction consisting of copper, carbon-modified TiO 2 , and sulfur-doped g-C 3 N 4 nanosheets (i.e., S-C 3 N 4 /Cu/C-TiO 2 ). The heterostructure affords a remarkable synergistic photocatalysis for tetracycline hydrochloride degradation, achieving an 82.6% removal efficiency within 30 min under visible light irradiation, about 15.4 and 7.3 times higher than that of S-C 3 N 4 and C-TiO 2 , respectively. The superior performance is attributed to the synergy between Cu doping and the Z-scheme heterojunction, which not only enhances the interfacial electric field effect, facilitating charge separation, but also boosts the redox capability. The charge carrier transfer between Cu/C-TiO 2 and S-C 3 N 4 follows a Z-scheme, as verified by trapping experiments, electron spin-resonance spectroscopy, and density functional theory calculations. Furthermore, the tetracycline hydrochloride degradation pathways are enunciated by liquid chromatograph mass spectrometry analysis. This work provides an effective approach for constructing high-performance photocatalysts that have potential in environmental remediation.

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ENVIRONMENTAL POLLUTION · 2024 · IF 7.6

Coupled effects of Fenton-like systems with different concentrations of H2O2/Biochar on diethyl phthalate removal: Dominant role of environmental persistent free radicals (EPFRs)

Jiawen Zhang,Shanjian Liu,Fupeng Huang,Dongmei Bi,Jie Song,Santao Chou

To investigate the impact of different H 2 O 2 concentrations on the Fenton-like systems of H 2 O 2 /biochar, this study examined the mechanism of the physical structure and environmental persistent free radicals (EPFRs) of biochar during diethyl phthalate (DEP) removal by the Fenton-like system. The peak-splitting method was utilized to differentiate EPFRs types in cotton stalk biochar produced at different temperatures. High-temperature environments promote π-electron delocalization, which facilitates phenyl π free radicals and σ-π oxygen-containing free radicals. By analyzing relationships between the removal rate K 1 and removal constant K obs of DEP with the structural properties of biochar, it was discovered that EPFRs concentrations in biochar had a significant positive correlation with K 1 (r = 0.92) and K obs (r = 0.97). Different H 2 O 2 concentrations added to the biochar removal system resulted in varied DEP removal efficiency. Among them, CS 500 , CS 550 , and CS 600 exhibited superior DEP removal efficiency when H 2 O 2 concentration was 5 mM.

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APPLIED CATALYSIS B-ENVIRONMENTAL · 2024 · IF 20.2

Developing carbon nitride with tailored defect structure for exceptional nonradical activation of peroxymonosulfate

Pei Yang,An Shen,Ziqi Zhu,Ling Wang,Kai Yang,Hongqi Dai,Haijiao Xie,Minzhi Chen,Xiaoyan Zhou

The nonradical activation of peroxymonosulfate (PMS) over nonmetallic catalyst remains a significant scientific challenge. Herein, we proposed a facile stepwise calcination approach to prepare fragmented carbon nitride (CN) with three coordinate nitrogen (N3 C ) vacancies (VCN). The defective structure comprising vacant and disintegrated nanosheet synergistically conferred VCN abundant unpaired electrons, providing an exceptional catalytic behavior to evolve nonradical pathway in PMS activation. This featured system allowed generating nonradical reactive species with 100 % selectivity, namely, a major singlet oxygenation and a spot of VCN/PMS complex-triggered oxidation, which enabled a high effectiveness in the degradation of Acid Orange 7 (almost 100 % removal efficiency within 20 min). Impressively, the VCN was also featured with excellent environment serviceability, long-term operational performance, and desirable non-photocatalytic efficiency in the PMS-mediated nonradical oxidation. Overall, this study offers a facile strategy for tailoring CN architecture to achieve PMS nonradical activation and contributes to an efficient strategy for wastewater remediation.

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FOOD HYDROCOLLOIDS · 2024 · IF 11

Double-layer films based on konjac gum and hydroxypropyl methyl cellulose loaded with thyme essential oil Pickering emulsion: Preparation, characterization, and application

Yingmeng Hou,Yuanda Sun,Shiyu Jia,Wentao Su,Shasha Cheng,Mingqian Tan,Haitao Wang

Due to the challenges posed by petroleum-based plastics in terms of degradation and their contribution to environmental pollution, researchers have focused on natural biodegradable packaging materials. Herein, a biodegradable, unidirectional released, bilayer active film based on Konjac gum/hydroxypropyl methylcellulose (KGM/HPMC) were developed. Specifically, Pickering nano-emulsion was formed via ultrasonic self-assembly of Thyme essential oil (TEO) and a suspension of oxidized chitin nanocrystals. The dual-network form by KGM/HPMC effectively incorporated the TEO droplets in Pickering nano-emulsion through intermolecular hydrogen bonding, demonstrating good solubility between the TEO droplets and film matrix. The mechanical properties of the active film are greatly improved due to the protective effect provided by the outer layer in the double-layer active emulsion film design. Furthermore, the double-layer active film enables a unidirectional release of essential oils, thereby enhancing the efficiency of essential oil utilization. In addition, the double-layer active film has beneficial properties, including antioxidation, antibacterial effects, ultraviolet radiation protection, and biodegradability compared to cling film. This film was employed for the preservation of salmon, and the findings indicated that the bilayer active film, formulated with 15% Pickering emulsion content, notably retarded the escalation of total volatile basic nitrogen (TVB-N) and pH levels in salmon. Furthermore, it successfully reduced the proportion of dominant bacteria (specifically Pseudomonas ) in salmon samples. The double-layer active film developed in this study demonstrates the potential for extending the shelf life of aquatic products.

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Frontiers in Chemistry · 2024 · IF 3.8

Dual-network fiber-hydrogel membrane for osmotic energy harvesting

Cao Licheng,Wu Huiqing

Osmotic energy harvesting was a promising way to alleviate energy crisis with reverse electrodialysis (RED) membrane-based technology. Charged hydrogel combined with other materials was an effective strategy to overcome problems, including restricted functional groups and complicated fabrication, but the effect of the respective charges of the two materials combined on the membrane properties has rarely been studied in depth. Herein, a new method was proposed that charged hydrogel was equipped with charged filter paper to form dual network fiber-hydrogel membrane for osmotic energy harvesting, which had excellent ion selectivity (beyond 0.9 under high concentration gradient), high ion transference number and energy conversion efficiency (beyond 32.5% under wide range concentration gradient), good property of osmotic energy conversion (∼4.84 W/m2 under 50-fold KCl and ∼6.75 W/m2 under simulated sea water and river water). Moreover, the power density was attributed to the surface-space charge synergistic effect from large amounts overlapping of electric double layer (EDL), so that the transmembrane ion transport was enhanced. It might be a valid mode to extensively develop the osmotic energy harvesting.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2024 · IF 5.8

Dual activation of peroxymonosulfate with FeS2@Co3O4-C catalyst and visible light for the efficient degradation of tetracycline

Xiyu Wang,Ying Lu,Gunel Imanova,Sridhar Komarneni,Jianfeng Ma

Antibiotics have garnered global attention as a pressing concern due to their wide spread discharge to the environment and resulting significant threats to both human health and the environment. The Sulfate Radical-based Advanced Oxidation Processes (SR-AOPs) technique has already been verified as an effective process for pollutant degradation. Herein, FeS 2 @Co 3 O 4 -C composites, utilizing ZIF-67-derived Co 3 O 4 -C as the substrate material, were fabricated using a single-step solvothermal technique for the degradation of tetracycline (TC) by activated peroxymonosulfate (PMS) in combination with visible light irradiation. In the FeS 2 @Co 3 O 4 -C/PMS/Vis system, the FeS 2 @Co 3 O 4 -C showed better activation performance than the single chemical activation system or photocatalytic system, with 97.2 % TC removed in 20 min. The FeS 2 @Co 3 O 4 -C composite material was thoroughly investigated employing X-ray diffraction (XRD) for analyzing its crystal structure, transmission electron microscopy (TEM) for detailed structural insights, scanning electron microscopy (SEM) for morphological examination, and X-ray photoelectron spectroscopy (XPS) for the elemental valence states. The quenching experiments, along with EPR test, revealed that the primary active oxygen species consisted of 1 O 2 , O 2 ·- , and h + . The results presented here suggest the impressive stability and recyclability of FeS 2 @Co 3 O 4 -C making it a potential candidate as an efficient catalyst for initiating the activation of PMS in degrading persistent organic pollutants present in water.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2024 · IF 7.7

Enhanced sorption and fluorescent detection of bisphenol A by using sodium alginate/cellulose nanofibrils/ZIF-8 composite hydrogel

Jiayu Ouyang,Xuefeng Zhang,Xinmiao Qi,Caichao Wang,Yao Yuan,Xiangjing Xie,Jianzheng Qiao,Xin Guo,Yiqiang Wu

To address the issue of bisphenol A (BPA) contamination in wastewater, a novel hydrogel, sodium alginate/cellulose nanofibrils/ZIF-8 composite hydrogel (SCZC), was synthesized for efficient BPA removal. The SCZC exhibited an exceptional adsorption capacity of 1696 mg/g, aligning well with both Langmuir and pseudo-second-order models. Furthermore, it exhibited remarkable regeneration properties, maintaining 89.1 % of its adsorption capacity even after undergoing five adsorption-desorption cycles. The synthesized SCZC also acted as a fluorescent sensor for detecting BPA, employing dynamic quenching and offering linear detection ranges of 10–100 mg/L and 0.2–1.0 μg/L, with a low detection limit of 0.06 μg/L. Analysis of adsorption and detection mechanisms revealed that SCZC's exceptional performance could be attributed to the three-dimensional (3D) porous structure formed by sodium alginate and cellulose nanofibrils. Economic analysis indicated that SCZC, in comparison to commercially activated carbon, was relatively inexpensive. This study introduces a novel approach for designing and preparing a sodium alginate-based hydrogel incorporating metal-organic frameworks, offering simultaneous BPA detection and removal capabilities.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2024 · IF 7.7

Collagen/functionalized cellulose nanofibril composite aerogels with pH-responsive characteristics for drug delivery system

Chengfei Yue,Changkun Ding,Min Hu,Ruquan Zhang,Bowen Cheng

In this work, carboxylated and amination modified cellulose nanofibrils (CNFs) were fabricated via the TEMPO catalytic oxidation system and diethylenetriamine, and collagen composite aerogels were fabricated through a simple self-assembly pretreatment and directional freeze-drying technology. Morphology analysis showed that the collagen composite aerogels had distinct layered-oriented double network structures after the self-assembly pretreatment. The intermolecular interactions between the collagen fibrils and functionalized CNFs (fCNFs) on the structures and properties of the composite aerogels were also examined through various characterization techniques. Water contact angle tests demonstrated the pH-responsive characteristics of the collagen/fCNF composite aerogels. Using 5-fluorouracil as the model drug, the pH-response mechanism was revealed. These results indicated that the collagen/fCNF composite aerogels exhibited excellent pH-responsive drug release capacities. Therefore, these pH-responsive collagen composite aerogels might have potential applications in industrial production in the biomedical, drug delivery, and tissue engineering fields.

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FOOD CHEMISTRY · 2024 · IF 8.5

Defective UiO-66/cellulose nanocomposite aerogel for the adsorption of heterocyclic aromatic amines

Qiyue Zhao,Hong-Man Hou,Gong-Liang Zhang,Hongshun Hao,Bei-wei Zhu,Jingran Bi

Heterocyclic aromatic amines (HAAs), arising as chemical derivatives during the high-temperature culinary treatment of proteinaceous comestibles, exhibit notable carcinogenic potential. In this paper, a composite aerogel (AG D-UiO-66 ) with high-capacity and fast adsorption of HAAs was made with anchoring defective UiO-66 (D-UiO-66) mediated by lauric acid on the backbone of cellulose nanofibers (CNF). AG D-UiO-66 with hierarchical porosity reduced the mass transfer efficiency for the adsorption of HAAs and achieved high adsorption amount (0.84–1.05 μmol/g) and fast adsorption (15 min). The isothermal adsorption model demonstrated that AG D-UiO-66 belonged to a multilayer adsorption mechanism for HAAs. Furthermore, AG D-UiO-66 was successfully used to adsorb 12 HAAs in different food (roasted beef, roasted pork, roasted salmon and marinade) with high recoveries of 94.65%–104.43%. The intrinsic potential of AG D-UiO-66 demonstrated that it could be widely applicable to the adsorption of HAAs in foods.

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MINERALS ENGINEERING · 2024 · IF 4.9

Degradation of thiosulfate ions in sodium aluminate solution photocatalyzed by Co-TiO2@ZIF-8

Jingyi Hao,Binchuan Li,Jing Dai,Daxue Fu,Yongfeng Chang,Jianshe Chen,Na Xu,Kuiren Liu,Qing Han

The strongly alkaline sodium aluminate solution generated from high-sulfur bauxites during their refinement through the Bayer process contains sulfur, mainly in the form of thiosulfate (S 2 O 3 2− ) ions, which affects the quality of the target product (alumina). Consequently, the large-scale use of high-sulfur bauxites is severely limited, and methods of desulfurizing sodium aluminate solutions are urgently needed. To address this need, we herein prepared metal–organic framework (ZIF-8)-supported Co-doped TiO 2 (Co-TiO 2 @ZIF-8) using a sol–gel method and low-temperature calcination under N 2 and examined the ability of this composite to photocatalyze the oxidative degradation of thiosulfate ions in sodium aluminate solutions. Co-TiO 2 @ZIF-8 retained the large specific surface area and rich porosity of ZIF-8, which reduced the agglomeration of TiO 2 particles on the surface. The loading of Co-TiO 2 endowed Co-TiO 2 @ZIF-8 with a mesoporous structure and thus increased its adsorption capacity. Compared with ZIF-8, Co-TiO 2 @ZIF-8 featured new functional groups, and the formation of Zn–C and N–Ti–O bonds confirmed the successful integration of Co-TiO 2 with the ZIF-8 carrier. Consequently, the thiosulfate removal rates by Co-TiO 2 @ZIF-8 were 42 % and 26 % higher than those observed for the blank sample and pure TiO 2 (light source = xenon arc lamp, oxidant = O 3 , reaction time = 60 min), respectively. This high performance is primarily due to Co doping, which enhanced the efficiency of visible light utilization, and the photogenerated electron–hole pairs on the photocatalyst surface and hydroxyl radicals formed by the interaction of holes with the solution-phase OH − ions.

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Nature Communications · 2024 ·Vol. 15 ·期 1 ·1-13 · IF 14.7

Cellulose nanofiber-mediated manifold dynamic synergy enabling adhesive and photo-detachable hydrogel for self-powered E-skin

Zhang Lei,Chen Lu,Wang Siheng,Wang Shanshan,Wang Dan,Yu Le,Xu Xu,Liu He,Chen Chaoji

Self-powered skin attachable and detachable electronics are under intense development to enable the internet of everything and everyone in new and useful ways. Existing on-demand separation strategies rely on complicated pretreatments and physical properties of the adherends, achieving detachable-on-demand in a facile, rapid, and universal way remains challenging. To overcome this challenge, an ingenious cellulose nanofiber-mediated manifold dynamic synergy strategy is developed to construct a supramolecular hydrogel with both reversible tough adhesion and easy photodetachment. The cellulose nanofiber-reinforced network and the coordination between Fe ions and polymer chains endow the dynamic reconfiguration of supramolecular networks and the adhesion behavior of the hydrogel. This strategy enables the simple and rapid fabrication of strong yet reversible hydrogels with tunable toughness ((Value max -Value min )/Value max of up to 86%), on-demand adhesion energy ((Value max -Value min )/Value max of up to 93%), and stable conductivity up to 12 mS cm −1 . We further extend this strategy to fabricate different cellulose nanofiber/Fe 3+ -based hydrogels from various biomacromolecules and petroleum polymers, and shed light on exploration of fundamental dynamic supramolecular network reconfiguration. Simultaneously, we prepare an adhesive-detachable triboelectric nanogenerator as a human-machine interface for a self-powered wireless monitoring system based on this strategy, which can acquire the real-time, self-powered monitoring, and wireless whole-body movement signal, opening up possibilities for diversifying potential applications in electronic skins and intelligent devices.

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