首页 > 最新文献

RSC sustainability最新文献

英文 中文
Salinity resistance and wind-enhanced evaporation of biomass-derived foam for sustainable solar desalination 耐盐性和风力增强的生物质衍生泡沫可持续太阳能脱盐
IF 4.9 Pub Date : 2025-11-11 DOI: 10.1039/D5SU00720H
Wei Wang, Xi Huan, Jingnan Wang, Siyuan Kang, Yuheng Li, Ziyu Tian, Yining Li, Xue Wang and Jiang Fan

Solar-driven interfacial water evaporation is a promising sustainable desalination strategy, but most research has been predominantly focused on material innovation and evaporation rate enhancement, while little attention has been paid to the impact of convective airflow on salt resistance and energy efficiency. Herein, a novel biomass-derived porous evaporator based on carbonized wild rice root (CWRR) with interconnected microchannels was fabricated. The obtained CWRR-based evaporator exhibited remarkable salt tolerance, with a stable evaporation rate of 1.12 kg m−2 h−1 in 10 wt% NaCl solution over 6 h at efficiencies reaching 82.1%. The addition of convective airflow further enhanced the evaporation performance in 3.5 wt% NaCl at 2 m s−1 wind speed to yield a sustained evaporation rate of 2.19 kg m−2 h−1 over 6 h at efficiencies reaching 94.3%, highlighting remarkable energy utilization. Further analysis of the data revealed that moderate airflows could optimize vapor diffusion while improving salt deposition, and excessive wind velocities could disrupt the evaporation balance state, thereby accumulating salt and declining efficiency. Overall, solar desalination can be optimized by combining environmental airflow control with sustainable biomass materials as a promising novel strategy for future advanced desalination devices.

太阳能驱动界面水蒸发是一种很有前途的可持续海水淡化策略,但大多数研究主要集中在材料创新和蒸发速率的提高上,而对流气流对盐阻力和能量效率的影响很少被关注。在此基础上,制备了一种基于碳化野生稻根(CWRR)的新型生物质多孔蒸发器,该蒸发器具有相互连接的微通道。所获得的cwrr蒸发器具有显著的耐盐性,在10 wt% NaCl溶液中稳定的蒸发速率为1.12 kg m−2 h−1,效率达到82.1%。在3.5 wt% NaCl条件下,在2 m s−1风速下,对流气流的加入进一步提高了蒸发性能,在6 h内的持续蒸发速率为2.19 kg m−2 h−1,效率达到94.3%,突出了显著的能量利用率。进一步分析表明,适度的气流可以优化水汽扩散,促进盐沉积,过大的风速会破坏蒸发平衡状态,导致盐积累,效率下降。总的来说,太阳能海水淡化可以通过将环境气流控制与可持续生物质材料相结合来优化,这是未来先进海水淡化装置的一种有前景的新策略。
{"title":"Salinity resistance and wind-enhanced evaporation of biomass-derived foam for sustainable solar desalination","authors":"Wei Wang, Xi Huan, Jingnan Wang, Siyuan Kang, Yuheng Li, Ziyu Tian, Yining Li, Xue Wang and Jiang Fan","doi":"10.1039/D5SU00720H","DOIUrl":"https://doi.org/10.1039/D5SU00720H","url":null,"abstract":"<p >Solar-driven interfacial water evaporation is a promising sustainable desalination strategy, but most research has been predominantly focused on material innovation and evaporation rate enhancement, while little attention has been paid to the impact of convective airflow on salt resistance and energy efficiency. Herein, a novel biomass-derived porous evaporator based on carbonized wild rice root (CWRR) with interconnected microchannels was fabricated. The obtained CWRR-based evaporator exhibited remarkable salt tolerance, with a stable evaporation rate of 1.12 kg m<small><sup>−2</sup></small> h<small><sup>−1</sup></small> in 10 wt% NaCl solution over 6 h at efficiencies reaching 82.1%. The addition of convective airflow further enhanced the evaporation performance in 3.5 wt% NaCl at 2 m s<small><sup>−1</sup></small> wind speed to yield a sustained evaporation rate of 2.19 kg m<small><sup>−2</sup></small> h<small><sup>−1</sup></small> over 6 h at efficiencies reaching 94.3%, highlighting remarkable energy utilization. Further analysis of the data revealed that moderate airflows could optimize vapor diffusion while improving salt deposition, and excessive wind velocities could disrupt the evaporation balance state, thereby accumulating salt and declining efficiency. Overall, solar desalination can be optimized by combining environmental airflow control with sustainable biomass materials as a promising novel strategy for future advanced desalination devices.</p>","PeriodicalId":74745,"journal":{"name":"RSC sustainability","volume":" 12","pages":" 5641-5652"},"PeriodicalIF":4.9,"publicationDate":"2025-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/su/d5su00720h?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145600783","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Innovative recycling strategies for non-recycled plastics: advancing the circular economy for a sustainable future 非再生塑料的创新回收战略:推进循环经济,实现可持续发展的未来
IF 4.9 Pub Date : 2025-11-04 DOI: 10.1039/D5SU00421G
Rajesh Kumar Srivastava, Prakash Kumar Sarangi, Akhilesh Kumar Singh, Ashna Parveen, Uttam Kumar Sahoo, Vinod V. T. Padil, Kasim Sakran Abass, Khurmatbek Jumaniyozov, Choo Wou Onn and Tonni Agustiono Kurniawan

Plastic waste presents a critical environmental challenge, with reports of global production surpassing 390 million tons annually and an effective recycling rate of less than 10%. This study investigates advanced recycling methodologies aimed at mitigating plastic waste and promoting a circular economy. Mechanical, chemical, and emerging advanced recycling technologies are evaluated based on efficiency, scalability, and environmental impact. Mechanical recycling achieves material recovery rates up to 60%, accompanied by a 30% reduction in greenhouse gas emissions compared to virgin plastic production; however, polymer contamination and degradation restrict its long-term effectiveness. Chemical recycling processes, including microwave-assisted pyrolysis and enzymatic plastic depolymerization, demonstrate recovery efficiencies exceeding 90%, producing high-quality feedstocks suitable for industrial reuse. Life-cycle assessments reveal that chemical recycling can reduce environmental footprints by approximately 45% relative to conventional disposal practices. Advanced recycling technologies, such as enzymatic and catalytic hydrocracking, blockchain-enabled plastic waste tracking, and bioplastic waste valorization conversion, exhibit conversion efficiencies ranging from 85 to 95%, though scalability remains limited by economic and technological constraints. Integration with digital innovations, such as AI-enabled waste sorting and blockchain-based supply chain transparency, enhances material recovery rates by up to 20%. Policy instruments, notably extended producer responsibility (EPR) schemes and consumer engagement initiatives, further reinforce recycling outcomes. Case studies from Europe and Asia demonstrate landfill diversion rates reaching 75%, underscoring the effectiveness of integrated approaches. The analysis highlights the urgent necessity for multifaceted recycling strategies to curb the escalating plastic waste crisis and facilitate a transition toward a sustainable circular economy. Through the strategic application of technological advancements and policy interventions, it is feasible to achieve a 50% reduction in global plastic waste by 2030, thereby contributing significantly to environmental protection and resource conservation, while mitigating climate change impacts.

据报道,全球塑料垃圾年产量超过3.9亿吨,有效回收率不到10%,这对环境构成了严峻挑战。本研究探讨了旨在减少塑料废物和促进循环经济的先进回收方法。机械、化学和新兴的先进回收技术基于效率、可扩展性和环境影响进行评估。机械回收实现材料回收率高达60%,与原始塑料生产相比,温室气体排放量减少30%;然而,聚合物污染和降解限制了其长期有效性。化学回收过程,包括微波辅助热解和酶促塑料解聚,显示回收效率超过90%,生产出适合工业再利用的高质量原料。生命周期评估显示,与传统处置做法相比,化学品回收可以减少约45%的环境足迹。先进的回收技术,如酶和催化加氢裂化、区块链支持的塑料废物跟踪和生物塑料废物增值转化,其转化效率从85%到95%不等,但可扩展性仍然受到经济和技术限制的限制。与数字创新相结合,如人工智能支持的废物分类和基于区块链的供应链透明度,可将材料回收率提高高达20%。政策工具,特别是扩大生产者责任(EPR)计划和消费者参与倡议,进一步加强了回收成果。欧洲和亚洲的个案研究显示,堆填区的分流率达75%,突显综合方法的成效。该分析强调,迫切需要采取多方面的回收战略,以遏制不断升级的塑料废物危机,并促进向可持续循环经济的过渡。通过战略性地应用技术进步和政策干预,到2030年实现全球塑料垃圾减少50%的目标是可行的,从而为环境保护和资源节约做出重大贡献,同时缓解气候变化的影响。
{"title":"Innovative recycling strategies for non-recycled plastics: advancing the circular economy for a sustainable future","authors":"Rajesh Kumar Srivastava, Prakash Kumar Sarangi, Akhilesh Kumar Singh, Ashna Parveen, Uttam Kumar Sahoo, Vinod V. T. Padil, Kasim Sakran Abass, Khurmatbek Jumaniyozov, Choo Wou Onn and Tonni Agustiono Kurniawan","doi":"10.1039/D5SU00421G","DOIUrl":"https://doi.org/10.1039/D5SU00421G","url":null,"abstract":"<p >Plastic waste presents a critical environmental challenge, with reports of global production surpassing 390 million tons annually and an effective recycling rate of less than 10%. This study investigates advanced recycling methodologies aimed at mitigating plastic waste and promoting a circular economy. Mechanical, chemical, and emerging advanced recycling technologies are evaluated based on efficiency, scalability, and environmental impact. Mechanical recycling achieves material recovery rates up to 60%, accompanied by a 30% reduction in greenhouse gas emissions compared to virgin plastic production; however, polymer contamination and degradation restrict its long-term effectiveness. Chemical recycling processes, including microwave-assisted pyrolysis and enzymatic plastic depolymerization, demonstrate recovery efficiencies exceeding 90%, producing high-quality feedstocks suitable for industrial reuse. Life-cycle assessments reveal that chemical recycling can reduce environmental footprints by approximately 45% relative to conventional disposal practices. Advanced recycling technologies, such as enzymatic and catalytic hydrocracking, blockchain-enabled plastic waste tracking, and bioplastic waste valorization conversion, exhibit conversion efficiencies ranging from 85 to 95%, though scalability remains limited by economic and technological constraints. Integration with digital innovations, such as AI-enabled waste sorting and blockchain-based supply chain transparency, enhances material recovery rates by up to 20%. Policy instruments, notably extended producer responsibility (EPR) schemes and consumer engagement initiatives, further reinforce recycling outcomes. Case studies from Europe and Asia demonstrate landfill diversion rates reaching 75%, underscoring the effectiveness of integrated approaches. The analysis highlights the urgent necessity for multifaceted recycling strategies to curb the escalating plastic waste crisis and facilitate a transition toward a sustainable circular economy. Through the strategic application of technological advancements and policy interventions, it is feasible to achieve a 50% reduction in global plastic waste by 2030, thereby contributing significantly to environmental protection and resource conservation, while mitigating climate change impacts.</p>","PeriodicalId":74745,"journal":{"name":"RSC sustainability","volume":" 12","pages":" 5433-5458"},"PeriodicalIF":4.9,"publicationDate":"2025-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/su/d5su00421g?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145600829","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Environmental assessment of natural and fourth-generation synthetic refrigerant blends for sustainable cooling in India 印度用于可持续冷却的天然和第四代合成制冷剂混合物的环境评估
IF 4.9 Pub Date : 2025-11-01 DOI: 10.1039/D5SU00597C
Sandhiya Lakshmanan, Ranjana Aggarwal, Vikas Kumar Maurya, Sauvik Hossain S. K. and Kriti Tyagi

Climate change is a critical global concern, driven in part by the continuous increase in greenhouse gas (GHG) emissions. The refrigeration and air conditioning industries significantly contribute to these emissions through the use of hydrofluorocarbons (HFCs), which are potent GHGs. This study evaluates the environmental impacts of natural and fourth-generation synthetic refrigerants to support the development of a sustainable cooling action plan for India. Focusing on low global warming potential (GWP) refrigerant blends, the study investigates the atmospheric oxidation pathways of HFOs—R1234yf, R1234ze(Z), R1234ze(E), and R1243yf—alongside propane, identifying a 90 : 10 propane–R1234yf blend as a promising alternative to R32 in residential split air conditioners up to 7 kW. Thermodynamic analysis reveals that this blend achieves a 15% improvement in both volumetric cooling capacity and coefficient of performance compared with R32 while significantly lowering GWP to the level of R1234yf. Environmental and economic assessments show that the blend emits approximately 5.1 tCO2e annually, which is 22 times lesser than R32, and offers cost benefits due to its reduced capital and environmental expenditures. The total environmental impact metric for the simulated blend indicates that CO2-equivalent emissions can be reduced up to 96% when R32 is replaced with the R1234yf + propane blend. Based on these findings, this study proposes key policy imperatives for accelerating the adoption of natural refrigerants in India, in alignment with the Kigali Amendment's HFC phasedown schedule.

气候变化是一个重要的全球问题,部分原因是温室气体(GHG)排放的持续增加。制冷和空调行业通过使用强效温室气体氢氟碳化合物(HFCs),大大增加了这些排放。本研究评估了天然和第四代合成制冷剂对环境的影响,以支持印度可持续制冷行动计划的制定。该研究着眼于低全球变暖潜能值(GWP)制冷剂混合物,研究了HFOs-R1234yf, R1234ze(Z), R1234ze(E)和r1243yf -以及丙烷的大气氧化途径,确定了90:10丙烷- r1234yf混合物是最大7 kW住宅分体式空调中R32的有前途的替代品。热力学分析表明,与R32相比,该混合物在体积冷却能力和性能系数方面都提高了15%,同时显著降低了GWP至R1234yf的水平。环境和经济评估表明,该混合燃料每年排放约5.1亿吨二氧化碳当量,比R32少22倍,并且由于其减少的资本和环境支出而具有成本效益。模拟混合物的总环境影响指标表明,当R32被R1234yf +丙烷混合物取代时,二氧化碳当量排放量可减少96%。基于这些发现,本研究根据《基加利修正案》的氢氟碳化物淘汰时间表,提出了在印度加速采用天然制冷剂的关键政策要求。
{"title":"Environmental assessment of natural and fourth-generation synthetic refrigerant blends for sustainable cooling in India","authors":"Sandhiya Lakshmanan, Ranjana Aggarwal, Vikas Kumar Maurya, Sauvik Hossain S. K. and Kriti Tyagi","doi":"10.1039/D5SU00597C","DOIUrl":"https://doi.org/10.1039/D5SU00597C","url":null,"abstract":"<p >Climate change is a critical global concern, driven in part by the continuous increase in greenhouse gas (GHG) emissions. The refrigeration and air conditioning industries significantly contribute to these emissions through the use of hydrofluorocarbons (HFCs), which are potent GHGs. This study evaluates the environmental impacts of natural and fourth-generation synthetic refrigerants to support the development of a sustainable cooling action plan for India. Focusing on low global warming potential (GWP) refrigerant blends, the study investigates the atmospheric oxidation pathways of HFOs—R1234yf, R1234ze(<em>Z</em>), R1234ze(<em>E</em>), and R1243yf—alongside propane, identifying a 90 : 10 propane–R1234yf blend as a promising alternative to R32 in residential split air conditioners up to 7 kW. Thermodynamic analysis reveals that this blend achieves a 15% improvement in both volumetric cooling capacity and coefficient of performance compared with R32 while significantly lowering GWP to the level of R1234yf. Environmental and economic assessments show that the blend emits approximately 5.1 tCO<small><sub>2</sub></small>e annually, which is 22 times lesser than R32, and offers cost benefits due to its reduced capital and environmental expenditures. The total environmental impact metric for the simulated blend indicates that CO<small><sub>2</sub></small>-equivalent emissions can be reduced up to 96% when R32 is replaced with the R1234yf + propane blend. Based on these findings, this study proposes key policy imperatives for accelerating the adoption of natural refrigerants in India, in alignment with the Kigali Amendment's HFC phasedown schedule.</p>","PeriodicalId":74745,"journal":{"name":"RSC sustainability","volume":" 12","pages":" 5665-5678"},"PeriodicalIF":4.9,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/su/d5su00597c?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145600785","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Assessing the environmental footprint of electrochromic windows: a comparative LCA with AI-based forecasting 评估电致变色窗的环境足迹:与人工智能预测相比较的LCA
IF 4.9 Pub Date : 2025-10-27 DOI: 10.1039/D5SU00638D
Mohsen Rabbani, Olivia Tahti, Sabinus Essel Arthur, Macy A. Hopping, Christopher J. Barile, Mohd Hassan Karim, Ario Fahimi and Ehsan Vahidi

This investigation assesses electrochromic windows as a novel green alternative to traditional double-pane windows through a life cycle assessment, which analyzes and compares both types of windows. The life cycle assessment was conducted using the impact categories of TRACI 2.1 in the SimaPro 9.1 application, with ecoinvent, and 1 m2 of each window type as the functional unit for the comparisons. The manufacturing of EC windows yielded a total CO2 generation of 49.6 kg CO2, and the manufacturing of double-pane windows resulted in 76.05 kg CO2. In the manufacturing of electrochromic glass windows, the float glass production process contributed 9.79 kg of CO2 at that stage of fabrication. From the sensitivity analysis, it was determined that using 10% less electricity during electrochromic window production can lower carbon emissions for electrochromic windows by 1.51 kg CO2. These life cycle assessment impact results were later used for advanced AI-predictive modeling using Python's scientific ecosystem, including PyTorch for neural network implementation, scikit-learn for data preprocessing and metric calculation, and custom-built hierarchical architectures to develop both Artificial Neural Network and Adaptive Neuro-Fuzzy Inference System models. Considering that 200 m2 of double-pane windows were replaced by electrochromic windows, the embodied impact of electrochromic window production would be offset by the operational impact of 30.1 t CO2 in 10.5 months. Since the lifespans of both window types are similar, electrochromic windows are promising green alternatives to double-pane windows.

本研究通过生命周期评估来评估电致变色窗作为传统双层窗的一种新型绿色替代品,并对两种类型的窗户进行了分析和比较。使用SimaPro 9.1应用程序中的TRACI 2.1影响类别进行生命周期评估,使用ecoinvent,每种窗口类型的1 m2作为比较的功能单元。制造EC窗产生的二氧化碳总量为49.6 kg,制造双层玻璃窗产生的二氧化碳总量为76.05 kg。在电致变色玻璃窗的制造过程中,浮法玻璃生产过程在制造阶段贡献了9.79千克的二氧化碳。通过敏感性分析,确定在电致变色窗生产过程中减少10%的电力,可使电致变色窗的碳排放量降低1.51 kg CO2。这些生命周期评估影响结果后来被用于使用Python的科学生态系统进行高级人工智能预测建模,包括用于神经网络实现的PyTorch,用于数据预处理和度量计算的scikit-learn,以及用于开发人工神经网络和自适应神经模糊推理系统模型的定制分层架构。考虑到200平方米的双层玻璃窗被电致变色窗所取代,电致变色窗生产的具体影响将被10.5个月的30.1吨二氧化碳的运营影响所抵消。由于两种窗户的寿命相似,电致变色窗户是有希望的绿色替代品,可以替代双层玻璃窗户。
{"title":"Assessing the environmental footprint of electrochromic windows: a comparative LCA with AI-based forecasting","authors":"Mohsen Rabbani, Olivia Tahti, Sabinus Essel Arthur, Macy A. Hopping, Christopher J. Barile, Mohd Hassan Karim, Ario Fahimi and Ehsan Vahidi","doi":"10.1039/D5SU00638D","DOIUrl":"https://doi.org/10.1039/D5SU00638D","url":null,"abstract":"<p >This investigation assesses electrochromic windows as a novel green alternative to traditional double-pane windows through a life cycle assessment, which analyzes and compares both types of windows. The life cycle assessment was conducted using the impact categories of TRACI 2.1 in the SimaPro 9.1 application, with ecoinvent, and 1 m<small><sup>2</sup></small> of each window type as the functional unit for the comparisons. The manufacturing of EC windows yielded a total CO<small><sub>2</sub></small> generation of 49.6 kg CO<small><sub>2</sub></small>, and the manufacturing of double-pane windows resulted in 76.05 kg CO<small><sub>2</sub></small>. In the manufacturing of electrochromic glass windows, the float glass production process contributed 9.79 kg of CO<small><sub>2</sub></small> at that stage of fabrication. From the sensitivity analysis, it was determined that using 10% less electricity during electrochromic window production can lower carbon emissions for electrochromic windows by 1.51 kg CO<small><sub>2</sub></small>. These life cycle assessment impact results were later used for advanced AI-predictive modeling using Python's scientific ecosystem, including PyTorch for neural network implementation, scikit-learn for data preprocessing and metric calculation, and custom-built hierarchical architectures to develop both Artificial Neural Network and Adaptive Neuro-Fuzzy Inference System models. Considering that 200 m<small><sup>2</sup></small> of double-pane windows were replaced by electrochromic windows, the embodied impact of electrochromic window production would be offset by the operational impact of 30.1 t CO<small><sub>2</sub></small> in 10.5 months. Since the lifespans of both window types are similar, electrochromic windows are promising green alternatives to double-pane windows.</p>","PeriodicalId":74745,"journal":{"name":"RSC sustainability","volume":" 12","pages":" 5653-5664"},"PeriodicalIF":4.9,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/su/d5su00638d?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145600784","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sustainable chemistry without borders: Highlights from an inaugural conference held at St Andrews in June 2025 无国界的可持续化学:2025年6月在圣安德鲁斯举行的首届会议的亮点
IF 4.9 Pub Date : 2025-10-24 DOI: 10.1039/D5SU90060C
Amit Kumar and David J. Cole-Hamilton

This report provides a brief synopsis of the inaugural International Conference on Sustainable Chemistry for Net Zero (ICSC-NZ), held at the University of St Andrews in June 2025.

本报告简要介绍了于2025年6月在圣安德鲁斯大学举行的首届国际零排放可持续化学会议(ICSC-NZ)。
{"title":"Sustainable chemistry without borders: Highlights from an inaugural conference held at St Andrews in June 2025","authors":"Amit Kumar and David J. Cole-Hamilton","doi":"10.1039/D5SU90060C","DOIUrl":"https://doi.org/10.1039/D5SU90060C","url":null,"abstract":"<p >This report provides a brief synopsis of the inaugural International Conference on Sustainable Chemistry for Net Zero (ICSC-NZ), held at the University of St Andrews in June 2025.</p>","PeriodicalId":74745,"journal":{"name":"RSC sustainability","volume":" 12","pages":" 5408-5409"},"PeriodicalIF":4.9,"publicationDate":"2025-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/su/d5su90060c?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145600735","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Electrocatalysis for energy conversion reactions 能量转换反应的电催化
IF 4.9 Pub Date : 2025-10-22 DOI: 10.1039/D5SU90061A
Zhenyu Sun

A graphical abstract is available for this content

此内容的图形摘要可用
{"title":"Electrocatalysis for energy conversion reactions","authors":"Zhenyu Sun","doi":"10.1039/D5SU90061A","DOIUrl":"https://doi.org/10.1039/D5SU90061A","url":null,"abstract":"<p >A graphical abstract is available for this content</p>","PeriodicalId":74745,"journal":{"name":"RSC sustainability","volume":" 12","pages":" 5406-5407"},"PeriodicalIF":4.9,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/su/d5su90061a?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145600827","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Green synthesis of jarosite nanoparticles for photocatalytic degradation of Rhodamine B under simulated sunlight radiation 模拟太阳辐射下绿色合成光催化降解罗丹明B的黄铁矾纳米颗粒
IF 4.9 Pub Date : 2025-10-21 DOI: 10.1039/D5SU00731C
Hui Wen Neo, Eslam M. Hamed, Fun Man Fung and Sam F. Y. Li

Green synthesis of efficient photocatalysts using agricultural waste is a promising approach toward sustainable wastewater treatment. In this work, magnetite (Fe3O4) and jarosite (KFe3(SO4)2(OH)6) nanoparticles were synthesized using banana peel extract as a natural reducing/stabilizing agent and potassium source under microwave-assisted conditions. The structural, optical, and magnetic properties of the nanoparticles were systematically characterized. Photocatalytic performance was evaluated for Rhodamine B (RhB) degradation under simulated sunlight irradiation, and reaction kinetics were analyzed using pseudo-first-order models. Jarosite exhibited a rate constant (k) of 0.0198 min−1, approximately double that of magnetite (k = 0.0098 min−1), achieving >99% RhB removal within 30 minutes. Mechanistic studies, including scavenger tests and photoluminescence analysis, confirmed the dominant role of ˙OH radicals and efficient charge separation in jarosite. The catalyst retained >94% activity over five cycles, and total organic carbon (TOC) removal reached 92%, indicating effective mineralization. This study demonstrates a low-cost, scalable, and environmentally friendly route for synthesizing iron-based photocatalysts, aligning with the UN Sustainable Development Goals (SDGs) for clean water and responsible consumption.

利用农业废弃物绿色合成高效光催化剂是一种很有前途的可持续废水处理方法。在微波辅助条件下,以香蕉皮提取物为天然还原/稳定剂和钾源合成了磁铁矿(Fe3O4)和黄铁矾(KFe3(SO4)2(OH)6)纳米颗粒。系统地表征了纳米颗粒的结构、光学和磁性能。在模拟日光照射下评价了光催化降解罗丹明B (Rhodamine B, RhB)的性能,并利用拟一阶模型分析了反应动力学。黄钾铁矾的速率常数(k)为0.0198 min−1,大约是磁铁矿(k = 0.0098 min−1)的两倍,在30分钟内实现了99%的RhB去除率。清除剂试验和光致发光分析等机理研究证实了黄铁矾中˙OH自由基和有效电荷分离的主导作用。催化剂在5个循环中保持了94%的活性,总有机碳(TOC)去除率达到92%,表明矿化有效。这项研究展示了一种低成本、可扩展、环保的合成铁基光催化剂的途径,符合联合国可持续发展目标(sdg)关于清洁水和负责任消费的目标。
{"title":"Green synthesis of jarosite nanoparticles for photocatalytic degradation of Rhodamine B under simulated sunlight radiation","authors":"Hui Wen Neo, Eslam M. Hamed, Fun Man Fung and Sam F. Y. Li","doi":"10.1039/D5SU00731C","DOIUrl":"https://doi.org/10.1039/D5SU00731C","url":null,"abstract":"<p >Green synthesis of efficient photocatalysts using agricultural waste is a promising approach toward sustainable wastewater treatment. In this work, magnetite (Fe<small><sub>3</sub></small>O<small><sub>4</sub></small>) and jarosite (KFe<small><sub>3</sub></small>(SO<small><sub>4</sub></small>)<small><sub>2</sub></small>(OH)<small><sub>6</sub></small>) nanoparticles were synthesized using banana peel extract as a natural reducing/stabilizing agent and potassium source under microwave-assisted conditions. The structural, optical, and magnetic properties of the nanoparticles were systematically characterized. Photocatalytic performance was evaluated for Rhodamine B (RhB) degradation under simulated sunlight irradiation, and reaction kinetics were analyzed using pseudo-first-order models. Jarosite exhibited a rate constant (<em>k</em>) of 0.0198 min<small><sup>−1</sup></small>, approximately double that of magnetite (<em>k</em> = 0.0098 min<small><sup>−1</sup></small>), achieving &gt;99% RhB removal within 30 minutes. Mechanistic studies, including scavenger tests and photoluminescence analysis, confirmed the dominant role of ˙OH radicals and efficient charge separation in jarosite. The catalyst retained &gt;94% activity over five cycles, and total organic carbon (TOC) removal reached 92%, indicating effective mineralization. This study demonstrates a low-cost, scalable, and environmentally friendly route for synthesizing iron-based photocatalysts, aligning with the UN Sustainable Development Goals (SDGs) for clean water and responsible consumption.</p>","PeriodicalId":74745,"journal":{"name":"RSC sustainability","volume":" 12","pages":" 5518-5526"},"PeriodicalIF":4.9,"publicationDate":"2025-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/su/d5su00731c?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145600759","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Low-capacitance pulsed discharge enables heat- and solvent-free delamination of lithium-ion battery cathodes 低电容脉冲放电使锂离子电池阴极的热和无溶剂分层
IF 4.9 Pub Date : 2025-10-21 DOI: 10.1039/D5SU00304K
Chiharu Tokoro, Moe Nakahara, Takatoshi Kurihara, Akiko Kubota, Mauricio Córdova-Udaeta, Asako Narita and Yutaro Takaya

Recovering cathode-active materials (CAMs) from end-of-life lithium-ion batteries without added heat or chemicals is pivotal for low-impact, closed-loop manufacturing. We show that circuit capacitance dictates whether a single electrical pulse yields clean, solvent-free delamination or destructive pulverization. Commercial Li(Ni0.33Mn0.33Co0.33)O2 coated on aluminum foil was exposed to 375–475 J discharges from 6.4 μF (low-C) and 400 μF (high-C) capacitor banks. The low-C circuit squeezed the stored energy into sub-200 μs current spikes (≈15 kA) that heated the CAM/Al interface from ambient to ≈500 K within 100 μs, generating transient stresses of tens of MPa before the foil was severed. A 425 J pulse cleanly lifted the entire coating (99.9 wt% CAMs), leaving only 0.3 wt% residual aluminum, and X-ray diffraction confirmed that the layered oxide structure remained intact. Conversely, the high-C circuit stretched the same energy over > 500 μs, diverting the current into the plasma and fragmenting both the foil and coating. The delamination plateaued near 90 wt%, and at 475 J, aluminum contamination surged nine-fold. One-dimensional transient heat-rise analysis corroborated that temporal energy concentration—enabled by low capacitance—triggers the instantaneous interfacial heating required for clean separation, whereas energy dispersion channels power into fragmentation. This heat- and solvent-free pre-treatment supplies battery-grade layered oxides ready for direct cathode recycling, eliminating the furnaces, acids, and wastewater typical of pyro- or hydrometallurgical routes.

从报废的锂离子电池中回收阴极活性材料(CAMs),而不增加热量或化学物质,对于低影响、闭环制造至关重要。我们表明,电路电容决定了单个电脉冲是产生干净的、无溶剂的分层还是破坏性的粉碎。在6.4 μF(低c)和400 μF(高c)电容组中,对涂覆在铝箔上的商用Li(Ni0.33Mn0.33Co0.33)O2进行375 ~ 475 J放电。低碳电路将储存的能量压缩成低于200 μs的电流尖峰(≈15 kA),在100 μs内将CAM/Al界面从室温加热到≈500 K,在箔被切断之前产生数十MPa的瞬态应力。425 J脉冲清除了整个涂层(99.9 wt% CAMs),只留下0.3 wt%残余铝,x射线衍射证实层状氧化物结构保持完整。相反,高c电路将相同的能量拉伸超过500 μs,将电流转移到等离子体中并使箔和涂层破碎。分层稳定在90%左右,在475 J时,铝污染激增了9倍。一维瞬态热升分析证实,由低电容实现的时间能量集中触发了清洁分离所需的瞬时界面加热,而能量分散则将能量输送到碎片中。这种无热和无溶剂的预处理提供了电池级的层状氧化物,为直接阴极回收做好了准备,消除了典型的热法或湿法冶金路线的熔炉、酸和废水。
{"title":"Low-capacitance pulsed discharge enables heat- and solvent-free delamination of lithium-ion battery cathodes","authors":"Chiharu Tokoro, Moe Nakahara, Takatoshi Kurihara, Akiko Kubota, Mauricio Córdova-Udaeta, Asako Narita and Yutaro Takaya","doi":"10.1039/D5SU00304K","DOIUrl":"https://doi.org/10.1039/D5SU00304K","url":null,"abstract":"<p >Recovering cathode-active materials (CAMs) from end-of-life lithium-ion batteries without added heat or chemicals is pivotal for low-impact, closed-loop manufacturing. We show that circuit capacitance dictates whether a single electrical pulse yields clean, solvent-free delamination or destructive pulverization. Commercial Li(Ni<small><sub>0</sub></small>.<small><sub>33</sub></small>Mn<small><sub>0</sub></small>.<small><sub>33</sub></small>Co<small><sub>0</sub></small>.<small><sub>33</sub></small>)O<small><sub>2</sub></small> coated on aluminum foil was exposed to 375–475 J discharges from 6.4 μF (low-C) and 400 μF (high-C) capacitor banks. The low-C circuit squeezed the stored energy into sub-200 μs current spikes (≈15 kA) that heated the CAM/Al interface from ambient to ≈500 K within 100 μs, generating transient stresses of tens of MPa before the foil was severed. A 425 J pulse cleanly lifted the entire coating (99.9 wt% CAMs), leaving only 0.3 wt% residual aluminum, and X-ray diffraction confirmed that the layered oxide structure remained intact. Conversely, the high-C circuit stretched the same energy over &gt; 500 μs, diverting the current into the plasma and fragmenting both the foil and coating. The delamination plateaued near 90 wt%, and at 475 J, aluminum contamination surged nine-fold. One-dimensional transient heat-rise analysis corroborated that temporal energy concentration—enabled by low capacitance—triggers the instantaneous interfacial heating required for clean separation, whereas energy dispersion channels power into fragmentation. This heat- and solvent-free pre-treatment supplies battery-grade layered oxides ready for direct cathode recycling, eliminating the furnaces, acids, and wastewater typical of pyro- or hydrometallurgical routes.</p>","PeriodicalId":74745,"journal":{"name":"RSC sustainability","volume":" 12","pages":" 5571-5579"},"PeriodicalIF":4.9,"publicationDate":"2025-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/su/d5su00304k?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145600762","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pyrolysis of orange peel waste to pyrofuels and pyrochar: optimization and techno-economic insights for industrial scale-up 橘皮废弃物热解制焦燃料和焦炭:工业规模的优化和技术经济见解
IF 4.9 Pub Date : 2025-10-16 DOI: 10.1039/D5SU00575B
Uma Sankar Behera, Sourav Poddar and Hun-Soo Byun

Biomass presents a sustainable alternative to fossil fuels; however, it faces limitations such as high moisture content, low bulk density, and poor grindability. This study investigates the pyrolysis of waste orange peels to produce pyro-char, pyro-oil, and pyro-gas, a process that has been rarely reported in the literature. The effects of pyrolysis temperature, feedstock mass, and heating rate on the yield of these pyro-products were systematically investigated. The biomass was characterized using proximate analysis and thermogravimetric analysis (TGA), while the pyro-products were analyzed for their higher heating value (HHV), lower heating value (LHV), morphology and elemental composition via scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX), and chemical composition using gas chromatography mass spectrometry (GC-MS). Critical parameters influencing the pyrolysis outcomes were identified: feedstock mass (1–3 kg), temperature (573–1173 K), and heating rate (10–30 K min−1). Under optimal conditions of 2 kg feedstock mass, 873 K temperature, and a heating rate of 20 K min−1, the theoretical yields were 26.52 wt% pyro-char, 22.76 wt% pyro-oil, and 50.72 wt% pyro-gas, with an overall process desirability of approximately 0.7. Experimental yields showed slight deviations, resulting in 28.12 wt% pyro-char, 22.89 wt% pyro-oil, and 48.99 wt% pyro-gas, all within a ±5.7% margin of the theoretical values. The estimated payback period for the initial investment is 1.3 years at a 10% discount rate, which is considerably shorter than the previously reported 6-year period for pyro-gas and pyro-oil production. Scale-up to larger plants is expected to further reduce this duration. This study bridges the gap in comprehensive techno-economic analyses of industrial-scale waste orange peel pyrolysis by producing pyro-char, pyro-oil, and pyro-gas, a three-product yield not previously reported. It offers a sustainable approach to valorizing orange peel waste into high-value products, aligning with Industry 5.0 principles and the United Nations 2030 Sustainable Development Goals.

生物质是化石燃料的可持续替代品;然而,它面临着水分含量高、堆积密度低、可磨性差等限制。本研究研究了废桔皮热解生成焦炭、焦油和焦气的过程,这一过程在文献中很少报道。研究了热解温度、原料质量和升温速率对热解产物收率的影响。采用近似分析(proximate analysis)和热重分析(TGA)对生物质进行了表征,通过扫描电子显微镜(SEM-EDX)和气相色谱-质谱(GC-MS)对热解产物的高热值(HHV)和低热值(LHV)进行了形貌和元素组成分析。确定了影响热解结果的关键参数:原料质量(1 - 3 kg)、温度(573-1173 K)和升温速率(10-30 K min−1)。在2kg原料质量、873 K温度和20 K min−1加热速率的最佳条件下,理论产率为26.52 wt%焦炭、22.76 wt%焦油和50.72 wt%焦气,总体工艺理想度约为0.7。实验产率显示出轻微的偏差,导致28.12 wt%的焦,22.89 wt%的焦油和48.99 wt%的焦气,都在理论值的±5.7%范围内。初始投资的预计投资回收期为1.3年,折扣率为10%,这比之前报道的6年的火气和火油生产周期短得多。规模扩大到更大的工厂预计将进一步缩短这一持续时间。这项研究填补了工业规模废橙皮热解生产焦炭、焦油和焦气的综合技术经济分析的空白,这三种产物的产量以前没有报道过。它提供了一种可持续的方法,将橙皮废物转化为高价值产品,符合工业5.0原则和联合国2030年可持续发展目标。
{"title":"Pyrolysis of orange peel waste to pyrofuels and pyrochar: optimization and techno-economic insights for industrial scale-up","authors":"Uma Sankar Behera, Sourav Poddar and Hun-Soo Byun","doi":"10.1039/D5SU00575B","DOIUrl":"https://doi.org/10.1039/D5SU00575B","url":null,"abstract":"<p >Biomass presents a sustainable alternative to fossil fuels; however, it faces limitations such as high moisture content, low bulk density, and poor grindability. This study investigates the pyrolysis of waste orange peels to produce pyro-char, pyro-oil, and pyro-gas, a process that has been rarely reported in the literature. The effects of pyrolysis temperature, feedstock mass, and heating rate on the yield of these pyro-products were systematically investigated. The biomass was characterized using proximate analysis and thermogravimetric analysis (TGA), while the pyro-products were analyzed for their higher heating value (HHV), lower heating value (LHV), morphology and elemental composition <em>via</em> scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX), and chemical composition using gas chromatography mass spectrometry (GC-MS). Critical parameters influencing the pyrolysis outcomes were identified: feedstock mass (1–3 kg), temperature (573–1173 K), and heating rate (10–30 K min<small><sup>−1</sup></small>). Under optimal conditions of 2 kg feedstock mass, 873 K temperature, and a heating rate of 20 K min<small><sup>−1</sup></small>, the theoretical yields were 26.52 wt% pyro-char, 22.76 wt% pyro-oil, and 50.72 wt% pyro-gas, with an overall process desirability of approximately 0.7. Experimental yields showed slight deviations, resulting in 28.12 wt% pyro-char, 22.89 wt% pyro-oil, and 48.99 wt% pyro-gas, all within a ±5.7% margin of the theoretical values. The estimated payback period for the initial investment is 1.3 years at a 10% discount rate, which is considerably shorter than the previously reported 6-year period for pyro-gas and pyro-oil production. Scale-up to larger plants is expected to further reduce this duration. This study bridges the gap in comprehensive techno-economic analyses of industrial-scale waste orange peel pyrolysis by producing pyro-char, pyro-oil, and pyro-gas, a three-product yield not previously reported. It offers a sustainable approach to valorizing orange peel waste into high-value products, aligning with Industry 5.0 principles and the United Nations 2030 Sustainable Development Goals.</p>","PeriodicalId":74745,"journal":{"name":"RSC sustainability","volume":" 12","pages":" 5527-5555"},"PeriodicalIF":4.9,"publicationDate":"2025-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/su/d5su00575b?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145600760","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sustainably transforming waste into valuable products with the chemical sciences 利用化学科学可持续地将废物转化为有价值的产品
IF 4.9 Pub Date : 2025-10-15 DOI: 10.1039/D5SU90055G
Stephen A. Matlin, Federico Rosei, Philippe Lambin and Lei Jin

A graphical abstract is available for this content

此内容的图形摘要可用
{"title":"Sustainably transforming waste into valuable products with the chemical sciences","authors":"Stephen A. Matlin, Federico Rosei, Philippe Lambin and Lei Jin","doi":"10.1039/D5SU90055G","DOIUrl":"https://doi.org/10.1039/D5SU90055G","url":null,"abstract":"<p >A graphical abstract is available for this content</p>","PeriodicalId":74745,"journal":{"name":"RSC sustainability","volume":" 11","pages":" 4852-4855"},"PeriodicalIF":4.9,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/su/d5su90055g?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145384681","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
RSC sustainability
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1