Advanced Sustainable Systems最新文献_第3页

Nano-Pozzolanic Reaction Empowering Sustainable Construction with Hydrogel 纳米波唑啉反应增强水凝胶可持续建筑

IF 6.5 3区材料科学

Advanced Sustainable Systems Pub Date : 2025-04-09 DOI: 10.1002/adsu.202401037

Min Kwan Kang, Dongkeon Lee, Nam-Il Won, Yong Ha Rhie, Youngbae Han, Beomjoo Yang, Jeong-Wook Oh, Yang Ho Na

{"title":"Nano-Pozzolanic Reaction Empowering Sustainable Construction with Hydrogel","authors":"Min Kwan Kang, Dongkeon Lee, Nam-Il Won, Yong Ha Rhie, Youngbae Han, Beomjoo Yang, Jeong-Wook Oh, Yang Ho Na","doi":"10.1002/adsu.202401037","DOIUrl":"https://doi.org/10.1002/adsu.202401037","url":null,"abstract":"In the pursuit of enhancing the environmental sustainability of concrete, a fundamental construction material, traditional approaches often emphasize minimizing maintenance requirements to extend lifespan and improve durability. Departing from these conventional strategies, an innovative method aimed at augmenting thermal insulation and eco-friendliness of building structures is proposed, which involves the integration of nanoclay (NC) hydrogel to confer multifunctionality upon cement materials. Within the hydrogel matrix, NC functions as an internal cross-linking agent, establishing robust bonds with cement through a surface pozzolanic reaction. Rigorous validation of this interaction is conducted through meticulous adhesion measurements, assessments of changes in bonding energy, and simulations of shear forces. Significantly, the bonded NC hydrogel, enriched with water, demonstrates a remarkable ability to supply essential moisture for the successful settlement and growth of aquatic organisms and moss. This comprehensive study underscores the potential of NC hydrogel as an invaluable material for establishing the foundations of thriving ecosystems, presenting a promising avenue for sustainable construction practices.","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"9 6","pages":""},"PeriodicalIF":6.5,"publicationDate":"2025-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144367494","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Tuning Interfacial Charge Transfer and Exploring Morphological Insight in Biocarbon/MoSe2 Heterostructures for Enhanced Photodegradation of Organic Pollutants 调节界面电荷转移和探索生物碳/MoSe2异质结构增强有机污染物光降解的形态学见解

IF 6.5 3区材料科学

Advanced Sustainable Systems Pub Date : 2025-04-08 DOI: 10.1002/adsu.202500048

Shivam Tyagi, Srishti Agarwal, Bikash Kumar Mahapatra, Bhaskar Kaviraj

{"title":"Tuning Interfacial Charge Transfer and Exploring Morphological Insight in Biocarbon/MoSe2 Heterostructures for Enhanced Photodegradation of Organic Pollutants","authors":"Shivam Tyagi, Srishti Agarwal, Bikash Kumar Mahapatra, Bhaskar Kaviraj","doi":"10.1002/adsu.202500048","DOIUrl":"https://doi.org/10.1002/adsu.202500048","url":null,"abstract":"Surface and interface engineering has been proven to be an essential strategy for designing more advanced photocatalysts with enhanced photocatalytic activity. Activated biocarbon derived from sugarcane bagasse (SB-C) is used as a supporting substrate with Molybdenum diselenide (MoSe2) to design the heterostructure photocatalyst to improve charge separation and interface charge transfer. Compared to individual MoSe2, synthesized from different techniques, and SB-C components, the SB-C/MoSe2 heterojunctions demonstrated a significantly enhanced ability to degrade different organic pollutants (including different organic dyes, organic solvent, and heavy metal) under visible light irradiation, achieving the best rate of 97.17% under 20 min of visible light irradiation for degrading methylene blue dye (MB), and organic solvent viz. Phenol SB-C/MoSe2 takes 120 mins to degrade 94.25%. This remarkable capability is driven by efficient interfacial charge transfer, a larger electrochemical surface area of 5402.85 cm2, a lower bandgap energy of 2.38 eV, and a reduced recombination rate of electron-hole pairs. SB-C/MoSe2 has shown an excellent stability of 99.35% up to four cycles. These results suggested the potential for developing a highly effective heterostructure photocatalyst suitable for treating industrial wastewater by harnessing visible-light-driven photocatalytic activity.","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"9 6","pages":""},"PeriodicalIF":6.5,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144367269","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

3D Controlled Growth of Binder-Free Manganese Ferrite Electrodes for High-Performance Hybrid Supercapacitor Device 高性能混合超级电容器器件中无粘结剂锰铁氧体电极的三维控制生长

IF 6.5 3区材料科学

Advanced Sustainable Systems Pub Date : 2025-04-08 DOI: 10.1002/adsu.202500067

Rushiraj P. Bhosale, Sambhaji S. Kumbhar, Shraddha B. Bhosale, Amar M. Patil, Seong C. Jun, Dhanashri S. Gaikwad, Umakant M. Patil, Chandrakant D. Lokhande, Vinayak S. Jamadade

{"title":"3D Controlled Growth of Binder-Free Manganese Ferrite Electrodes for High-Performance Hybrid Supercapacitor Device","authors":"Rushiraj P. Bhosale, Sambhaji S. Kumbhar, Shraddha B. Bhosale, Amar M. Patil, Seong C. Jun, Dhanashri S. Gaikwad, Umakant M. Patil, Chandrakant D. Lokhande, Vinayak S. Jamadade","doi":"10.1002/adsu.202500067","DOIUrl":"https://doi.org/10.1002/adsu.202500067","url":null,"abstract":"The remarkable electrochemical features and promise for improved performance of binder-free manganese ferrite have attracted a lot of research interest in hybrid energy storage devices. The fine-tuning of preparative parameters has a significant impact on energy-storing performance, with deposition time appearing as a crucial parameter in enhancing their electrochemical properties. This work offers a simple and scalable method for the preparation of manganese ferrite with varying deposition times using chemical bath deposition (CBD). Varying deposition time results in a transformation from the manganese ferrite hydrate (MnFe2O4.H2O) to manganese ferrite (MnFe2O4) cubic structure and alteration in morphology from tetrahedral crystals to octahedral-like in MnFe2O4 series thin films (C-MFO). The MnFe2O4 electrode with an optimal deposition time of 7 h (C-MFO3) sample, featuring a cube-like morphology, achieves a maximum specific capacitance (Cs) of 491.2 F g−1 at 1.5 A g−1, maintaining 81.1% retention. Furthermore, the constructed hybrid supercapacitor device (HSD) exhibits a high Cs of 73.3 F g−1, along with a specific energy (SE) of 36.7 Wh kg−1 at a specific power (SP) of 1.7 kW kg−1. This work introduces a scalable method for producing binder-free manganese ferrite electrodes, suitable for use as cathodes in hybrid energy storage devices for practical applications.","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"9 6","pages":""},"PeriodicalIF":6.5,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144367272","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Human Energy Harvesting – A Flexible Bionic Composite MTEG-TENG Based on the Shared Substrate with Characteristic Doping 人体能量收集——基于共享衬底和特征掺杂的柔性仿生复合材料MTEG-TENG

IF 6.5 3区材料科学

Advanced Sustainable Systems Pub Date : 2025-04-08 DOI: 10.1002/adsu.202500116

Changxin Liu, Tong Shao, Zhenyao Ma, Yuncong Wang, Kailin Lei, Zhijie Hao, Zheng Sui

{"title":"Human Energy Harvesting – A Flexible Bionic Composite MTEG-TENG Based on the Shared Substrate with Characteristic Doping","authors":"Changxin Liu, Tong Shao, Zhenyao Ma, Yuncong Wang, Kailin Lei, Zhijie Hao, Zheng Sui","doi":"10.1002/adsu.202500116","DOIUrl":"https://doi.org/10.1002/adsu.202500116","url":null,"abstract":"Traditional wearable devices for underwater exploration face significant energy supply challenges, impacting mission efficiency and safety. To address this, the study introduces an innovative composite energy harvesting method that integrates a flexible micro thermoelectric generator and a triboelectric nanogenerator (MTEG-TENG) within a shared substrate architecture. This study also develops a theoretical model of energy harvesting based on human thermal and kinetic energy. A prototype is created, featuring a flexible bionic seagrass-like TENG (BS-TENG) and a flexible bionic leaf-like MTEG (BL-MTEG), integrated with an energy management unit. A method for preparing Bi2Te3-based thermoelectric materials through characteristic doping is proposed, enhancing the thermoelectric conversion performance. Through the implementation of an innovative thermal interface optimization scheme, the BL-MTEG unit achieves a 30% increase in output performance. In the experimental setup involving a temperature gradient of 20k, swing angular speed of 0.5π rad s−1, and a swing angle of 60°, the prototype successfully powers 51 LEDs and enables the information transmission of the Bluetooth module after processing through the energy harvesting circuit. This performance not only validates the effectiveness of the thermal interface design strategy but also provides a new approach for developing self-powered technology for underwater wearable devices.","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"9 6","pages":""},"PeriodicalIF":6.5,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144367453","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Nb, O Co-Doped Argyrodite Electrolytes with Enhanced Moisture and Lithium Stability for All-Solid-State Lithium Batteries 全固态锂电池中具有增强水分和锂稳定性的Nb， O共掺杂银镁石电解质

IF 6.5 3区材料科学

Advanced Sustainable Systems Pub Date : 2025-04-08 DOI: 10.1002/adsu.202500041

Jinghui Chen, Jing Zhang, Panlei Cao, Haichuan Yu, Ni Zhang, Xiayin Yao

{"title":"Nb, O Co-Doped Argyrodite Electrolytes with Enhanced Moisture and Lithium Stability for All-Solid-State Lithium Batteries","authors":"Jinghui Chen, Jing Zhang, Panlei Cao, Haichuan Yu, Ni Zhang, Xiayin Yao","doi":"10.1002/adsu.202500041","DOIUrl":"https://doi.org/10.1002/adsu.202500041","url":null,"abstract":"Argyrodite electrolytes with high ionic conductivity and excellent processability have garnered significant attention in the field of all-solid-state lithium batteries. However, their limited air stability and poor lithium compatibility impede the practical application in all-solid-state lithium batteries. Herein, a series of Li6P1−xNbxS5−2.5xO2.5xCl (x = 0, 0.025, 0.05, 0.075, and 0.1) solid electrolytes are synthesized by co-doping Nb and O in Li6PS5Cl electrolyte, showing simultaneously enhanced ionic conductivity, air stability, and interfacial compatibility with lithium. Benefitting from the substitution of P5+ with a larger radius Nb5+, the powder cold-pressed ionic conductivity of Li6P0.95Nb0.05S4.875O0.125Cl electrolyte reaches up to 4.19 mS cm−1 at room temperature. Moreover, the amount of H2S released by Li6P0.95Nb0.05S4.875O0.125Cl electrolyte is only half of the original electrolyte under a moist atmosphere with 30% relative humidity for 30 min, demonstrating improved moisture stability. Meanwhile, due to the formation of ionic conductor Li3OCl between the Li6P0.95Nb0.05S4.875O0.125Cl electrolyte and lithium, a critical current density (CCD) of 1.55 mA cm−2 and excellent cycling stability of 3600 h at a current density of 0.2 mA cm−2 can be realized. The resultant LiCoO2/Li6P0.95Nb0.05S4.875O0.125Cl/Li batteries exhibit prominent capacity and cycling stability, with a capacity of 85.9 mAh g−1 and 83.5% capacity retention after 1000 cycles at 1C.","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"9 6","pages":""},"PeriodicalIF":6.5,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144367270","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Tin Phosphide Hollow Nanospheres Enveloped by MXene as a Conversion-Type Anode Enabling Rapid and Stable Ion Storage in Diverse Energy Storage Systems 由MXene包裹的磷化锡空心纳米球作为转换型阳极，可在多种储能系统中实现快速稳定的离子存储

IF 6.5 3区材料科学

Advanced Sustainable Systems Pub Date : 2025-04-07 DOI: 10.1002/adsu.202500087

Qunbo Hui, Wufeng Fan, Xiaohong Xia, Hongbo Liu

{"title":"Tin Phosphide Hollow Nanospheres Enveloped by MXene as a Conversion-Type Anode Enabling Rapid and Stable Ion Storage in Diverse Energy Storage Systems","authors":"Qunbo Hui, Wufeng Fan, Xiaohong Xia, Hongbo Liu","doi":"10.1002/adsu.202500087","DOIUrl":"https://doi.org/10.1002/adsu.202500087","url":null,"abstract":"The design of a single anode material compatible with both Li⁺ and Na⁺ storage represents a critical advancement in the development of advanced lithium-ion (LIBs) and sodium-ion batteries (SIBs), particularly from a cost-effectiveness perspective. Tin phosphide, a conversion-type anode material, presents an energy storage mechanism without specific constraints on ion size or alloy properties and can provide high capacity with respect to Li and Na ions, making it an ideal candidate for dual applications in both LIBs and SIBs. However, its large volumetric expansion during the conversion reaction and low electronic conductivity lead to rapid capacity degradation. Herein, a coated hollow Sn4P3 sphere structure is designed, wherein Sn4P3 hollow nanospheres (Sn4P3HNs) are tightly encapsulated by MXene nanosheets. The hollow nanosphere structure provides space for inward volumetric expansion, while the MXene coating prevents outward expansion and enhances conductivity, endowing the composite with excellent cyclic stability and rate capabilities. For lithium-ion storage and sodium-ion storage, it exhibits excellent capacity retention of 92.75% and 95% at 1 A g−1 after 1200 and 1500 cycles, respectively. The remarkable electrochemical properties demonstrated in this study indicate that this composite is a highly competitive anode option for simultaneous application in lithium-ion and sodium-ion batteries.","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"9 6","pages":""},"PeriodicalIF":6.5,"publicationDate":"2025-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144367212","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Facile Functionalization of Separator with an Amino Acid to Boost Li–S Battery Performance 氨基酸对隔膜的简单功能化以提高锂- s电池性能

IF 6.5 3区材料科学

Advanced Sustainable Systems Pub Date : 2025-04-03 DOI: 10.1002/adsu.202500076

Lulu Ren, Ying Guo, Justin Zhong, Chunhua Ying, Jin Liu, Wei-Hong Zhong

{"title":"Facile Functionalization of Separator with an Amino Acid to Boost Li–S Battery Performance","authors":"Lulu Ren, Ying Guo, Justin Zhong, Chunhua Ying, Jin Liu, Wei-Hong Zhong","doi":"10.1002/adsu.202500076","DOIUrl":"https://doi.org/10.1002/adsu.202500076","url":null,"abstract":"Lithium-sulfur (Li–S) batteries are hindered by issues such as the polysulfide shuttle effect and Li dendrite formation, which leads to capacity degradation. To address these issues, a bio-strategy involving the functionalization of a commercial separator with an amino acid-polymer system, leucine-polyacrylic acid (Leu-PAA), is reported here. A simple soaking method is used in preparing the separator with the Leu-PAA, which is effective and viable for practical application. The Leu-PAA soaked separator exhibits improved wettability and thermal stability, as well as enhanced polysulfide trapping and regulated lithium ion flux. As a result, Li–S cell using the separator with Leu-PAA achieves an initial capacity of 599.9 mAh g−1 at 0.5 A g−1 and retains 53.5% of capacity after 500 cycles. The enhanced properties are attributed to the synergistic effects of Leu and PAA, which suppress the shuttle effect and ensure uniform ion transport, resulting in improved electrochemical performance. This work provides a promising, bio-inspired solution for improving the performance and cycle life of Li–S batteries.","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"9 6","pages":""},"PeriodicalIF":6.5,"publicationDate":"2025-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/adsu.202500076","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144367267","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

0.09 wt.% Ru Enables Robust Bifunctional Water Splitting on Co-N4 Sites 0.09 wt.% Ru能在Co-N4位点上实现稳健的双功能水分解

IF 6.5 3区材料科学

Advanced Sustainable Systems Pub Date : 2025-04-03 DOI: 10.1002/adsu.202500111

Shiyi Li, Chen Liang, Keyu Wang, Linfeng Lei, Linzhou Zhuang, Zhi Xu

{"title":"0.09 wt.% Ru Enables Robust Bifunctional Water Splitting on Co-N4 Sites","authors":"Shiyi Li, Chen Liang, Keyu Wang, Linfeng Lei, Linzhou Zhuang, Zhi Xu","doi":"10.1002/adsu.202500111","DOIUrl":"https://doi.org/10.1002/adsu.202500111","url":null,"abstract":"The development of high-performance bifunctional electrocatalysts for the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is crucial for efficient and cost-effective water splitting in sustainable hydrogen production. A significant challenge in this area is engineering active sites that maintain robust stability and high activity under the varying electrochemical conditions encountered in both alkaline and acidic media. This study presents Co80Ru1-NCNFs, an advanced bifunctional electrocatalyst that showcases a self-supported carbon nanofiber membrane with uniformly dispersed Ru-modified Co-N4 active sites, excelling in both OER and HER. The trace incorporation of Ru (0.09 wt%) significantly enhances catalytic activity and stability through synergistic Co/Ru interactions. Co80Ru1-NCNFs demonstrate promising OER performance in 1.0 m KOH, along with remarkable HER activity in both alkaline and acidic conditions. Density functional theory (DFT) calculations reveal that Ru incorporation optimizes the adsorption energies of reaction intermediates on the Co-N4 active sites, thereby improving reaction kinetics. This work provides critical insights for the design and development of efficient and stable bifunctional electrocatalysts for sustainable energy conversion.","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"9 6","pages":""},"PeriodicalIF":6.5,"publicationDate":"2025-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144367266","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Metal-Free Carbon Catalysts Derived From Industrial Lignin for Efficient Alcohols Oxidation 工业木质素制备的高效醇氧化无金属碳催化剂

IF 6.5 3区材料科学

Advanced Sustainable Systems Pub Date : 2025-04-01 DOI: 10.1002/adsu.202500191

Yuhan Wang, Anzheng Zhang, Shuhao Chen, Zhaorui Hua, Jie Jiang, Long Cheng, Jing Luo, Huidong Liu, Juan Meng, Hengfei Qin

{"title":"Metal-Free Carbon Catalysts Derived From Industrial Lignin for Efficient Alcohols Oxidation","authors":"Yuhan Wang, Anzheng Zhang, Shuhao Chen, Zhaorui Hua, Jie Jiang, Long Cheng, Jing Luo, Huidong Liu, Juan Meng, Hengfei Qin","doi":"10.1002/adsu.202500191","DOIUrl":"https://doi.org/10.1002/adsu.202500191","url":null,"abstract":"A comprehensive understanding of the electronic structure of catalytic active centers and their nearby environments is essential for clarifying the link structure and activity. This understanding can facilitate the design and development of novel metal-free carbon-based materials with desirable catalytic properties from industrial lignin waste. In this research, phosphorus (P) or nitrogen (N) atoms are incorporated into sulfur (S)-doped porous carbon using a highly effective collosol doping carbonization method, which alters the electronic configuration of the active sites and enhances catalytic performance. The P and S co-doped porous carbon (SPC) demonstrates remarkable effectiveness in the oxidation of benzyl alcohol (BA), reaching a high conversion rate of 96.6% within 2 h and benzaldehyde (BAD) yield of 92.5%, along with a turnover frequency (TOF) value of 8.6 × 10−3 mol·g−1·h−1. It also exhibits strong catalytic selectivity for other functionalized alcohols. Density functional theory calculations (DFT) indicate that the incorporation of P or N atom into S-doped porous carbon increases the electron density at the Fermi level and modifies Mulliken charge distributions at the active sites, enhancing cooperative electron regulation and catalytic activity, particularly in the P and S co-doping structures. These findings offer guidance for the design of advanced metal-free carbon catalysts.","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"9 6","pages":""},"PeriodicalIF":6.5,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144367139","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Hydrochar-Based Wood Bio-Adhesives from Sewage Sludge: The Role of Sodium Periodate Oxidation 污水污泥中烃基木质生物胶粘剂：高碘酸钠氧化的作用

IF 6.5 3区材料科学

Advanced Sustainable Systems Pub Date : 2025-04-01 DOI: 10.1002/adsu.202500137

Rui Dou, Fan Gao, Wen-Xue Jiang, Ping Chen, Yong-Xing Chen, Li-Jian Leng, Zhi-Xiang Xu

{"title":"Hydrochar-Based Wood Bio-Adhesives from Sewage Sludge: The Role of Sodium Periodate Oxidation","authors":"Rui Dou, Fan Gao, Wen-Xue Jiang, Ping Chen, Yong-Xing Chen, Li-Jian Leng, Zhi-Xiang Xu","doi":"10.1002/adsu.202500137","DOIUrl":"https://doi.org/10.1002/adsu.202500137","url":null,"abstract":"The development of technologies for replacing formaldehyde-based adhesives and disposing of sewage sludge (SS) are two standing issues of high interest to the academy and industry. This study reports the production of formaldehyde-free wood bio-adhesive using hydrochar from hydrothermal carbonization of SS aided by sodium periodate (NaIO4) oxidation. The performance of the bio-adhesives can meet the requirements of the Chinese National Standard GB/T 9846-2015 (≥0.7 MPa). The aldehyde group forms after NaIO4 treatment of sewage sludge hydrochar, which should benefit adhesion performance. However, the oxidation process also breaks some polysaccharides' carbon chains, disrupting the extracellular polymeric substances (EPS) structure in hydrochar and forming small molecular compounds. As a result, the wet shear strength value of bio-adhesive decreases, but the water resistance increases. Nevertheless, the interaction between active functional groups (e.g., between the aldehyde and amine groups) in bio-adhesives during hot-pressing treatment promotes adhesion performance. In addition, after doping polyethyleneimine, the cross-linked network in bio-adhesives can be further enhanced, improving the wet shear strength and water resistance. Hence, introducing active functional groups is the key step to bio-adhesives, proving NaIO4 oxidation as a novel and practical approach to valorize sewage sludge for producing formaldehyde-free adhesives.","PeriodicalId":7294,"journal":{"name":"Advanced Sustainable Systems","volume":"9 6","pages":""},"PeriodicalIF":6.5,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144367140","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0