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Ionic adaptive network: A sustainable route to replace synthetic rubbers with natural polymers for high-temperature applications
IF 8.6 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2025-01-07 DOI: 10.1016/j.susmat.2025.e01243
Subhradeep Mandal , Osvalds Verners , Eric Euchler , Arpita Kundu , Cordelia Zimmerer , Ricardo Bernhardt , Toshio Tada , Gert Heinrich , Sven Wießner , Amit Das
Natural rubber (NR) is a biopolymer consisting of cis-1,4-isoprene units extracted from the sap of rubber trees, mainly Hevea Brasiliensis. This rubber is widely used in the automotive and other industries due to its performance and elasticity. However, synthetic rubber has largely replaced natural rubber in many applications because of the poor heat resistance of natural rubber. On the other hand, non-recyclable sulfur-based synthetic rubber composites pose a major environmental issue from the viewpoint of sustainability. In this report, a flexible (non-directional) crosslinking network based on ionic bonds in modified natural rubber (epoxy-modified NR) using dicarboxylic acid and dimethylimidazole (DMI) is presented, which eliminates the disadvantages of natural rubber and outperforms synthetic rubber without compromising its mechanical performance. Accelerated aging, temperature scanning stress relaxation, compression set, and temperature-dependent FT-IR analyses confirm the high thermal stability of ionically crosslinked natural elastomer. The ionic crosslinked rubber shows a significant improvement in initial degradation temperature (196 °C) compared to thermally stable synthetic elastomers, such as NBR (acrylonitrile butadiene rubber), CR (polychloroprene rubber), and peroxide-cured EPDM (ethylene propylene diene monomer). Unlike sulfur-cured elastomers, the ionically crosslinked natural rubber exhibits superior cut growth resistance and self-repairing capabilities, as demonstrated by X-ray microtomography. These findings, along with the natural origin of the developed crosslinked elastomers, can reduce environmental damage and the carbon footprint associated with sulfur-cured and petroleum-based synthetic rubber products.
{"title":"Ionic adaptive network: A sustainable route to replace synthetic rubbers with natural polymers for high-temperature applications","authors":"Subhradeep Mandal ,&nbsp;Osvalds Verners ,&nbsp;Eric Euchler ,&nbsp;Arpita Kundu ,&nbsp;Cordelia Zimmerer ,&nbsp;Ricardo Bernhardt ,&nbsp;Toshio Tada ,&nbsp;Gert Heinrich ,&nbsp;Sven Wießner ,&nbsp;Amit Das","doi":"10.1016/j.susmat.2025.e01243","DOIUrl":"10.1016/j.susmat.2025.e01243","url":null,"abstract":"<div><div>Natural rubber (NR) is a biopolymer consisting of cis-1,4-isoprene units extracted from the sap of rubber trees, mainly <em>Hevea Brasiliensis</em>. This rubber is widely used in the automotive and other industries due to its performance and elasticity. However, synthetic rubber has largely replaced natural rubber in many applications because of the poor heat resistance of natural rubber. On the other hand, non-recyclable sulfur-based synthetic rubber composites pose a major environmental issue from the viewpoint of sustainability. In this report, a flexible (non-directional) crosslinking network based on ionic bonds in modified natural rubber (epoxy-modified NR) using dicarboxylic acid and dimethylimidazole (DMI) is presented, which eliminates the disadvantages of natural rubber and outperforms synthetic rubber without compromising its mechanical performance. Accelerated aging, temperature scanning stress relaxation, compression set, and temperature-dependent FT-IR analyses confirm the high thermal stability of ionically crosslinked natural elastomer. The ionic crosslinked rubber shows a significant improvement in initial degradation temperature (196 °C) compared to thermally stable synthetic elastomers, such as NBR (acrylonitrile butadiene rubber), CR (polychloroprene rubber), and peroxide-cured EPDM (ethylene propylene diene monomer). Unlike sulfur-cured elastomers, the ionically crosslinked natural rubber exhibits superior cut growth resistance and self-repairing capabilities, as demonstrated by X-ray microtomography. These findings, along with the natural origin of the developed crosslinked elastomers, can reduce environmental damage and the carbon footprint associated with sulfur-cured and petroleum-based synthetic rubber products.</div></div>","PeriodicalId":22097,"journal":{"name":"Sustainable Materials and Technologies","volume":"43 ","pages":"Article e01243"},"PeriodicalIF":8.6,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143137430","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Biomass waste-assisted upcycling consumed poly(ethylene terephthalate) into functional nanocarbon composites for high-efficiency adsorption
IF 8.6 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2025-01-06 DOI: 10.1016/j.susmat.2025.e01241
Xing Zhou , Dexiang Li , Lan Yang , Yuying Shao , Xuyang Li , Rubai Luo , Yang Li , Yangyang Lin
Converting waste plastics into high-value carbon materials is one of the most promising solutions for upcycling the waste resources and significant environmental concern. Herein, we have enhanced the carbonization yield through a designed one-step strategy involving the pre-mixing of KOH with consumed polyethylene terephthalate (PET). It was further applied to the co‑carbonization of consumed PET with woody biomass waste to produce functional carbon materials. The carbon materials exhibit remarkable adsorption capabilities, achieving up to 529.3 mg/g for methylene blue and 368.5 mg/g for methyl orange, as well as significant adsorption capacity of 3.03 mmol/g for CO2, which are much higher than many reported adsorbents. This work proposes a facile method for upcycling consumed PET and woody biomass waste, presenting a significant strategy for achieving high-valuable potential application.
{"title":"Biomass waste-assisted upcycling consumed poly(ethylene terephthalate) into functional nanocarbon composites for high-efficiency adsorption","authors":"Xing Zhou ,&nbsp;Dexiang Li ,&nbsp;Lan Yang ,&nbsp;Yuying Shao ,&nbsp;Xuyang Li ,&nbsp;Rubai Luo ,&nbsp;Yang Li ,&nbsp;Yangyang Lin","doi":"10.1016/j.susmat.2025.e01241","DOIUrl":"10.1016/j.susmat.2025.e01241","url":null,"abstract":"<div><div>Converting waste plastics into high-value carbon materials is one of the most promising solutions for upcycling the waste resources and significant environmental concern. Herein, we have enhanced the carbonization yield through a designed one-step strategy involving the pre-mixing of KOH with consumed polyethylene terephthalate (PET). It was further applied to the co‑carbonization of consumed PET with woody biomass waste to produce functional carbon materials. The carbon materials exhibit remarkable adsorption capabilities, achieving up to 529.3 mg/g for methylene blue and 368.5 mg/g for methyl orange, as well as significant adsorption capacity of 3.03 mmol/g for CO<sub>2</sub>, which are much higher than many reported adsorbents. This work proposes a facile method for upcycling consumed PET and woody biomass waste, presenting a significant strategy for achieving high-valuable potential application.</div></div>","PeriodicalId":22097,"journal":{"name":"Sustainable Materials and Technologies","volume":"43 ","pages":"Article e01241"},"PeriodicalIF":8.6,"publicationDate":"2025-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143137468","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Triphenylamine-porphyrin conjugates as antenna modular systems towards the detection of 1-hexanol through surface photovoltage under UV and visible light illumination using the scanning Kelvin probe
IF 8.6 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2025-01-06 DOI: 10.1016/j.susmat.2025.e01239
Prasanth Palanisamy , Mageshwari Anandan , Sheethal Sasi , Arbacheena Bora , Rence P Reji , Sarath Kumar Chedharla Balaji , Yoshiyuki Kawazoe , Gurusamy Raman , Surya Velappa Jayaraman , Yuvaraj Sivalingam , Venkatramaiah Nutalapati
Two modular porphyrin systems containing triphenylamine (TPA) unit at meso position of freebase porphyrin (H2TPAP) and its metalation with Zn(II) as ZnTPAP is developed to ascertain the role of antenna effect on the photo induced energy transfer process. H2TPAP and ZnTPAP exhibited a significant electronic overlap between peripheral TPA and porphyrin π-system to demonstrate its strong donor behaviour in solid-state thin films. Porphyrin ensembles change their surface photovoltages towards recognition of various VOCs (like ethanol, acetone, 1-hexanol, triethylamine, nonanal, and acetonitrile) as observed through photophysical and excited-state gas-phase interaction studies using Scanning Kelvin Probe (SKP). The chemical sensitivity towards the surface potential is monitored under dark, UV and visible light illuminations. Both H2TPAP and ZnTPAP exhibited to show different behaviour with high selectivity towards 1-hexanol vapours. Under UV light illumination at 365 nm, ZnTPAP exhibited a rapid response (99 %) within 1 s and good recovery (54 %) within 96 s. Under visible light (QTH), the response and recovery decreased due to sequential photo-induced energy and electron transfer processes. Further, density functional theory results confirm that both H2TPAP and ZnTPAP show more affinity towards alcohol vapours compared to other VOCs. Molecular interactions including donor-donor and hydrogen bonding interactions in tandem contribute to the intriguing response to 1-hexanol and enhance the photo response of ZnTPAP over H2TPAP.
{"title":"Triphenylamine-porphyrin conjugates as antenna modular systems towards the detection of 1-hexanol through surface photovoltage under UV and visible light illumination using the scanning Kelvin probe","authors":"Prasanth Palanisamy ,&nbsp;Mageshwari Anandan ,&nbsp;Sheethal Sasi ,&nbsp;Arbacheena Bora ,&nbsp;Rence P Reji ,&nbsp;Sarath Kumar Chedharla Balaji ,&nbsp;Yoshiyuki Kawazoe ,&nbsp;Gurusamy Raman ,&nbsp;Surya Velappa Jayaraman ,&nbsp;Yuvaraj Sivalingam ,&nbsp;Venkatramaiah Nutalapati","doi":"10.1016/j.susmat.2025.e01239","DOIUrl":"10.1016/j.susmat.2025.e01239","url":null,"abstract":"<div><div>Two modular porphyrin systems containing triphenylamine (TPA) unit at <em>meso</em> position of freebase porphyrin (H<sub>2</sub>TPAP) and its metalation with Zn(II) as ZnTPAP is developed to ascertain the role of antenna effect on the photo induced energy transfer process. H<sub>2</sub>TPAP and ZnTPAP exhibited a significant electronic overlap between peripheral TPA and porphyrin π-system to demonstrate its strong donor behaviour in solid-state thin films. Porphyrin ensembles change their surface photovoltages towards recognition of various VOCs (like ethanol, acetone, 1-hexanol, triethylamine, nonanal, and acetonitrile) as observed through photophysical and excited-state gas-phase interaction studies using Scanning Kelvin Probe (SKP). The chemical sensitivity towards the surface potential is monitored under dark, UV and visible light illuminations. Both H<sub>2</sub>TPAP and ZnTPAP exhibited to show different behaviour with high selectivity towards 1-hexanol vapours. Under UV light illumination at 365 nm, ZnTPAP exhibited a rapid response (99 %) within 1 s and good recovery (54 %) within 96 s. Under visible light (QTH), the response and recovery decreased due to sequential photo-induced energy and electron transfer processes. Further, density functional theory results confirm that both H<sub>2</sub>TPAP and ZnTPAP show more affinity towards alcohol vapours compared to other VOCs. Molecular interactions including donor-donor and hydrogen bonding interactions in tandem contribute to the intriguing response to 1-hexanol and enhance the photo response of ZnTPAP over H<sub>2</sub>TPAP.</div></div>","PeriodicalId":22097,"journal":{"name":"Sustainable Materials and Technologies","volume":"43 ","pages":"Article e01239"},"PeriodicalIF":8.6,"publicationDate":"2025-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143137471","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A highly stable co-doping induced phase structural transformation Sr-free oxygen electrode for reversible solid oxide cells
IF 8.6 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2025-01-06 DOI: 10.1016/j.susmat.2025.e01240
Xu Han , Qi Shao , Xiuyang Qian , Zhengpeng Chen , Yuan Gao , Xuemei Ou , Kun Zheng , Zhe Lv , Yihan Ling
(La,Sr)MnO3+δ (LSM)-based perovskite oxides have attracted great attention as oxygen electrodes for reversible solid oxide cells (RSOCs) owing to excellent comprehensive properties. Herein, we reported a Sr-free LaMn0.6Co0.2Cu0.2O3-δ (LMCC622) oxide without the side effects of Sr-containing oxygen electrodes and then characterized the electrochemical performance. The coupling of multiple Mn-site transition metal cations in LaMnO3+δ can result in the phase transition from the hexagonal perovskite to the orthorhombic perovskite. The increased thermal reduction of Mn ions in operation temperature releases large amounts of lattice oxygen, dramatically enhancing the catalytic activity of the oxygen electrode. Prepared anode-supported single cells with LMCC622 oxygen electrode exhibited high electrochemical performance (851.12 mW cm−2 at 800 °C), which is higher than that of La0.8Sr0.2MnO3-δ oxygen electrode (682.18 mW cm−2 at 800 °C). The further composite Gd0.1Ce0.9O1.95 (GDC) to LMCC622-GDC as oxygen electrode achieves excellent performance (1211.10 mW cm−2 at 800 °C) and stable cyclable operation of over 100 h in fuel cell and electrolysis cell mode.
{"title":"A highly stable co-doping induced phase structural transformation Sr-free oxygen electrode for reversible solid oxide cells","authors":"Xu Han ,&nbsp;Qi Shao ,&nbsp;Xiuyang Qian ,&nbsp;Zhengpeng Chen ,&nbsp;Yuan Gao ,&nbsp;Xuemei Ou ,&nbsp;Kun Zheng ,&nbsp;Zhe Lv ,&nbsp;Yihan Ling","doi":"10.1016/j.susmat.2025.e01240","DOIUrl":"10.1016/j.susmat.2025.e01240","url":null,"abstract":"<div><div>(La,Sr)MnO<sub>3+δ</sub> (LSM)-based perovskite oxides have attracted great attention as oxygen electrodes for reversible solid oxide cells (RSOCs) owing to excellent comprehensive properties. Herein, we reported a Sr-free LaMn<sub>0.6</sub>Co<sub>0.2</sub>Cu<sub>0.2</sub>O<sub>3-δ</sub> (LMCC622) oxide without the side effects of Sr-containing oxygen electrodes and then characterized the electrochemical performance. The coupling of multiple Mn-site transition metal cations in LaMnO<sub>3+δ</sub> can result in the phase transition from the hexagonal perovskite to the orthorhombic perovskite. The increased thermal reduction of Mn ions in operation temperature releases large amounts of lattice oxygen, dramatically enhancing the catalytic activity of the oxygen electrode. Prepared anode-supported single cells with LMCC622 oxygen electrode exhibited high electrochemical performance (851.12 mW cm<sup>−2</sup> at 800 °C), which is higher than that of La<sub>0.8</sub>Sr<sub>0.2</sub>MnO<sub>3-δ</sub> oxygen electrode (682.18 mW cm<sup>−2</sup> at 800 °C). The further composite Gd<sub>0.1</sub>Ce<sub>0.9</sub>O<sub>1.95</sub> (GDC) to LMCC622-GDC as oxygen electrode achieves excellent performance (1211.10 mW cm<sup>−2</sup> at 800 °C) and stable cyclable operation of over 100 h in fuel cell and electrolysis cell mode.</div></div>","PeriodicalId":22097,"journal":{"name":"Sustainable Materials and Technologies","volume":"43 ","pages":"Article e01240"},"PeriodicalIF":8.6,"publicationDate":"2025-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143137469","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Interchangeable films made from cellulose acetate and different types of carbon nanotubes with humidity sensing capabilities
IF 8.6 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2025-01-04 DOI: 10.1016/j.susmat.2025.e01237
Madalina Elena Bistriceanu , Andreea Laura Chibac-Scutaru , Florin Tudorache , Sufeng Zhang , Sergiu Coseri
This study presents a novel manufacturing technique for cellulose-based/multi-walled carbon nanotube film (CMF), which produces high-performance, flexible humidity sensors with fast reaction sensing in response to the growing need for wearable technology and environmental monitoring. The technique allows for the production of several kinds of sensors by varying the substrates on which the carbon nanotubes are attached. Because of its exceptional intrinsic qualities as well as its ability to produce films, cellulose acetate was chosen as a support for the implementation of this assembly. Furthermore, we have a great deal of structural flexibility with cellulose acetate since it is easily transformed into cellulose and then into carboxyl cellulose by TEMPO-mediated oxidation. Thus, depending on the chemical structure of each type of substrate, this structural diversity will produce sensors with varying sensitivity and functionality. Furthermore, the range of the examined samples has been further extended by the addition of amino groups to the nanotubes by chemical functionalization. The cellulose-based/CNT films exhibit a response time of only 100 s and demonstrate high reversibility, with sample recovery times exceeding 150 s. Considering these promising results, a wide range of application areas, including wearable technology, environmental tracking, and artificial skin, hold great potential for this straightforward manufacturing technique.
{"title":"Interchangeable films made from cellulose acetate and different types of carbon nanotubes with humidity sensing capabilities","authors":"Madalina Elena Bistriceanu ,&nbsp;Andreea Laura Chibac-Scutaru ,&nbsp;Florin Tudorache ,&nbsp;Sufeng Zhang ,&nbsp;Sergiu Coseri","doi":"10.1016/j.susmat.2025.e01237","DOIUrl":"10.1016/j.susmat.2025.e01237","url":null,"abstract":"<div><div>This study presents a novel manufacturing technique for cellulose-based/multi-walled carbon nanotube film (CMF), which produces high-performance, flexible humidity sensors with fast reaction sensing in response to the growing need for wearable technology and environmental monitoring. The technique allows for the production of several kinds of sensors by varying the substrates on which the carbon nanotubes are attached. Because of its exceptional intrinsic qualities as well as its ability to produce films, cellulose acetate was chosen as a support for the implementation of this assembly. Furthermore, we have a great deal of structural flexibility with cellulose acetate since it is easily transformed into cellulose and then into carboxyl cellulose by TEMPO-mediated oxidation. Thus, depending on the chemical structure of each type of substrate, this structural diversity will produce sensors with varying sensitivity and functionality. Furthermore, the range of the examined samples has been further extended by the addition of amino groups to the nanotubes by chemical functionalization. The cellulose-based/CNT films exhibit a response time of only 100 s and demonstrate high reversibility, with sample recovery times exceeding 150 s. Considering these promising results, a wide range of application areas, including wearable technology, environmental tracking, and artificial skin, hold great potential for this straightforward manufacturing technique.</div></div>","PeriodicalId":22097,"journal":{"name":"Sustainable Materials and Technologies","volume":"43 ","pages":"Article e01237"},"PeriodicalIF":8.6,"publicationDate":"2025-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143137428","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Significantly enhanced electrocaloric performance in lead-free BaTiO3 ceramics by introducing high-entropy component
IF 8.6 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2025-01-03 DOI: 10.1016/j.susmat.2025.e01235
Yingzhi Meng , Zhaojie Wang , Silin Tang , Xiang Niu , Yuleng Jiang , Xu Li , Hongfang Zhang , Dingyuan Wang , Yisong Bai , Biaolin Peng , Xue Chen , Sheng-Guo Lu , Qingqing Ke , Laijun Liu
Achieving high-performance electrocaloric (ECE) cooling technology to replace traditional compressor refrigeration can significantly alleviate environmental pollution. However, attaining both a large ECE and an ultra-wide working temperature range near ambient temperature remains challenging. Herein, we report a high-entropy strategy for obtaining high-performance ECE by constructing a binary system of (1-x)Ba0.9Ca0.1TiO3-xBaTa0.2Nb0.2Sc0.2In0.2Hf0.2O3. The ECE properties are significantly enhanced by the outstanding ferroelectric properties of the introduced high-entropy component (BaTa0.2Nb0.2Sc0.2In0.2Hf0.2O3). Our results demonstrate a large ECE of ΔTmax = 1.77 K and an ultra-wide working temperature range of 114 K (ΔT > 85 % ΔTmax) near room temperature in the x = 0.1 components. This approach can be applied broadly and greatly expands the range of candidate materials with high-performance ECE in lead-free systems.
{"title":"Significantly enhanced electrocaloric performance in lead-free BaTiO3 ceramics by introducing high-entropy component","authors":"Yingzhi Meng ,&nbsp;Zhaojie Wang ,&nbsp;Silin Tang ,&nbsp;Xiang Niu ,&nbsp;Yuleng Jiang ,&nbsp;Xu Li ,&nbsp;Hongfang Zhang ,&nbsp;Dingyuan Wang ,&nbsp;Yisong Bai ,&nbsp;Biaolin Peng ,&nbsp;Xue Chen ,&nbsp;Sheng-Guo Lu ,&nbsp;Qingqing Ke ,&nbsp;Laijun Liu","doi":"10.1016/j.susmat.2025.e01235","DOIUrl":"10.1016/j.susmat.2025.e01235","url":null,"abstract":"<div><div>Achieving high-performance electrocaloric (ECE) cooling technology to replace traditional compressor refrigeration can significantly alleviate environmental pollution. However, attaining both a large ECE and an ultra-wide working temperature range near ambient temperature remains challenging. Herein, we report a high-entropy strategy for obtaining high-performance ECE by constructing a binary system of (1-<em>x</em>)Ba<sub>0.9</sub>Ca<sub>0.1</sub>TiO<sub>3</sub>-<em>x</em>BaTa<sub>0.2</sub>Nb<sub>0.2</sub>Sc<sub>0.2</sub>In<sub>0.2</sub>Hf<sub>0.2</sub>O<sub>3</sub>. The ECE properties are significantly enhanced by the outstanding ferroelectric properties of the introduced high-entropy component (BaTa<sub>0.2</sub>Nb<sub>0.2</sub>Sc<sub>0.2</sub>In<sub>0.2</sub>Hf<sub>0.2</sub>O<sub>3</sub>). Our results demonstrate a large ECE of Δ<em>T</em><sub>max</sub> = 1.77 K and an ultra-wide working temperature range of 114 K (Δ<em>T</em> &gt; 85 % Δ<em>T</em><sub>max</sub>) near room temperature in the <em>x</em> = 0.1 components. This approach can be applied broadly and greatly expands the range of candidate materials with high-performance ECE in lead-free systems.</div></div>","PeriodicalId":22097,"journal":{"name":"Sustainable Materials and Technologies","volume":"43 ","pages":"Article e01235"},"PeriodicalIF":8.6,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143137467","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nitrogen-doped biochar loaded Cu2O/Cu7S4 to activate H2O2 for degradation of ibuprofen: Influencing factors and degradation mechanism
IF 8.6 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2025-01-03 DOI: 10.1016/j.susmat.2025.e01233
Kaihong Cao, Guangrong Liu, Jinli Zhai, Fangyue Chen, Zhihe Yang, Xin Jin, Bangheng Jin, Zilin Huang, Zekun Xu, Long Tong, Mingrui Cao, Qiang Huang
In this work, walnut green husks were pyrolyzed to biochar in the presence of copper ammonium sulfate to fabricate N-doped biochar-loaded Cu2O and Cu7S4 (Cu2O/Cu7S4/BC). This approach simultaneously achieved heteroatom doping and loading copper oxide and polysulfide on biochar through one-pot pyrolysis. Cu2O/Cu7S4/BC can activate H2O2 to degrade ibuprofen in water with 100 % removal and 46 % mineralization. This study optimized the dosage of reactants and investigated the effects of water background factors on the degradation efficiency of ibuprofen. It is found that a weakly alkaline (pH 7–9) favors the removal of ibuprofen and, HCO3 slightly inhibited the reaction efficiency while high concentrations of Cl can enhance the degradation. The effect of humic acid is related to its concentration in the solution. The degradation of ibuprofen is mainly attributed to the hydroxy radical 1O2. The efficient Cu(I)/Cu(II) redox cycle ensured the continuous production of these reactive oxygen species. The sulfur anions and pyridinic-N on the catalyst surface mediate the electron transfer during catalysis, accelerating the Cu(I)/Cu(II) cycle. At least 15 intermediate products were detected in the reaction residue, five of which were assessed to have higher toxicity to aquatic organisms than IBP. This work provides a method using biomass wastes to manufacture value-added materials for removing emerging organic pollutants and helps understand the mechanism of Cu/BC-based catalysts for the H2O2 activation.
{"title":"Nitrogen-doped biochar loaded Cu2O/Cu7S4 to activate H2O2 for degradation of ibuprofen: Influencing factors and degradation mechanism","authors":"Kaihong Cao,&nbsp;Guangrong Liu,&nbsp;Jinli Zhai,&nbsp;Fangyue Chen,&nbsp;Zhihe Yang,&nbsp;Xin Jin,&nbsp;Bangheng Jin,&nbsp;Zilin Huang,&nbsp;Zekun Xu,&nbsp;Long Tong,&nbsp;Mingrui Cao,&nbsp;Qiang Huang","doi":"10.1016/j.susmat.2025.e01233","DOIUrl":"10.1016/j.susmat.2025.e01233","url":null,"abstract":"<div><div>In this work, walnut green husks were pyrolyzed to biochar in the presence of copper ammonium sulfate to fabricate N-doped biochar-loaded Cu<sub>2</sub>O and Cu<sub>7</sub>S<sub>4</sub> (Cu<sub>2</sub>O/Cu<sub>7</sub>S<sub>4</sub>/BC). This approach simultaneously achieved heteroatom doping and loading copper oxide and polysulfide on biochar through one-pot pyrolysis. Cu<sub>2</sub>O/Cu<sub>7</sub>S<sub>4</sub>/BC can activate H<sub>2</sub>O<sub>2</sub> to degrade ibuprofen in water with 100 % removal and 46 % mineralization. This study optimized the dosage of reactants and investigated the effects of water background factors on the degradation efficiency of ibuprofen. It is found that a weakly alkaline (pH 7–9) favors the removal of ibuprofen and, HCO<sub>3</sub><sup>−</sup> slightly inhibited the reaction efficiency while high concentrations of Cl<sup>−</sup> can enhance the degradation. The effect of humic acid is related to its concentration in the solution. The degradation of ibuprofen is mainly attributed to the hydroxy radical <sup>1</sup>O<sub>2</sub>. The efficient Cu(I)/Cu(II) redox cycle ensured the continuous production of these reactive oxygen species. The sulfur anions and pyridinic-N on the catalyst surface mediate the electron transfer during catalysis, accelerating the Cu(I)/Cu(II) cycle. At least 15 intermediate products were detected in the reaction residue, five of which were assessed to have higher toxicity to aquatic organisms than IBP. This work provides a method using biomass wastes to manufacture value-added materials for removing emerging organic pollutants and helps understand the mechanism of Cu/BC-based catalysts for the H<sub>2</sub>O<sub>2</sub> activation.</div></div>","PeriodicalId":22097,"journal":{"name":"Sustainable Materials and Technologies","volume":"43 ","pages":"Article e01233"},"PeriodicalIF":8.6,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143138154","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Characterization of physicochemical properties and techno-economic analysis of cellulose nanocrystals derived from pilot production of sweet potato residue
IF 8.6 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2025-01-02 DOI: 10.1016/j.susmat.2024.e01232
Shunshun Zhu , Hongnan Sun , Taihua Mu , Aurore Richel
Cellulose nanocrystals (CNCs) have attracted great interest because of the unique structural characteristics and physical and chemical properties, but their high cost limited the application. The purpose of this study was to achieve the pilot-scale production of cellulose and CNCs by using sweet potato residue (SPR) as the main raw material. Meanwhile, based on the process of preparing CNCs from commercial acid hydrolyzed wood, a systematic economic benefit comparison was conducted on the production of CNCs from SPR. The results showed that the degree of polymerization of the cellulose produced was 475. CNCs was produced from SPR cellulose, and the CNCs had a rod-like structure, with the diameter and length ranging from 15.10 to 30.90 nm and 80.80–259.90 nm respectively. CNCs was a type I cellulose structure with high crystallinity, and the introduction of the amine characteristic peak (1665 cm−1) proved the successful production of CNCs. The maximum thermal degradation temperature of CNCs was 347.88 °C, and the zeta potential was −40.07 mV, which made it suitable for use as a reinforcing material in environmental protection bio-composites. The total capital investment to produce commercial CNCs was $227.74 million, while the total capital investment for CNCs from SPR was $203.34 million. Compared with commercial CNCs, the trial production of CNCs was more financially profitable and its net present value was higher. The use of SPR had both economic and environmental benefits, reducing the use of fossil fuels. These results are helpful in guiding the high-value utilization of other agricultural by-products and the further development of CNCs composites.
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引用次数: 0
Green synthesis of a ZnO/ZnS-decorated magnetic porous carbon hybrid for enhanced rhodamine B adsorption and photodegradation: A combined DFT and experimental study
IF 8.6 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2024-12-31 DOI: 10.1016/j.susmat.2024.e01231
Mobin Safarzadeh Khosrowshahi , Shiva Abdolhosein Hariri , Mohammad Rahimi , Hosein Banna Motejadded Emrooz , Farzaneh Shemirani
An important and sought-after goal in wastewater treatment is to develop photocatalysts that can effectively eliminate emerging contaminants while remaining environmentally sustainable. Semiconductor-based photocatalysis presents a promising solution for wastewater purification, offering advantages such as safety, efficiency, and cost-effectiveness. This study employs a green self-activation method to synthesize a hybrid magnetic porous carbon composite, decorated with Fe3O4, ZnO, and ZnS (PZZF), aimed at the degradation of Rhodamine B. A variety of characterization techniques were employed in this study, including XRD, nitrogen adsorption-desorption analysis, FESEM, FTIR, HRTEM, Zeta potential, Raman spectroscopy, contact angle measurements, DRS, Mott-Schottky analysis, and VSM. HRTEM confirmed the successful formation of heterojunction structures with the desired chemical compositions. The specific surface area of the synthesized material was measured to be 313 m2.g−1, and the saturation magnetization was found to be 13.51 emu.g−1. The investigation of PZZF's photocatalytic activity against Rhodamine B highlights its enhanced efficiency, particularly under UV/H2O2 treatment, leading to complete degradation of the dye within 60 min. Several factors affecting the degradation process were explored, including pH, catalyst dosage, H2O2 concentration, and scavenger studies, providing comprehensive insight into the optimal conditions for maximum photocatalytic performance. The results from the radical trapping experiments demonstrated that hydroxyl radicals played a critical role in the degradation of Rhodamine B. Additionally, the total organic carbon (TOC) analysis showed that more than 96 % of the carbon in the RhB solution was effectively mineralized into CO2 after 90 min of UV irradiation. DFT calculation results were aligned with experimental findings to validate theoretical predictions and enhance the overall understanding of the adsorption process. Ultimately, the UMAP technique was employed to visualize RhB adsorption and degradation by clustering and screening various configurations of the photocatalyst. These findings confirm the strong potential of the PZZF photocatalyst for effective dye degradation, highlighting its promising application in environmental remediation.
{"title":"Green synthesis of a ZnO/ZnS-decorated magnetic porous carbon hybrid for enhanced rhodamine B adsorption and photodegradation: A combined DFT and experimental study","authors":"Mobin Safarzadeh Khosrowshahi ,&nbsp;Shiva Abdolhosein Hariri ,&nbsp;Mohammad Rahimi ,&nbsp;Hosein Banna Motejadded Emrooz ,&nbsp;Farzaneh Shemirani","doi":"10.1016/j.susmat.2024.e01231","DOIUrl":"10.1016/j.susmat.2024.e01231","url":null,"abstract":"<div><div>An important and sought-after goal in wastewater treatment is to develop photocatalysts that can effectively eliminate emerging contaminants while remaining environmentally sustainable. Semiconductor-based photocatalysis presents a promising solution for wastewater purification, offering advantages such as safety, efficiency, and cost-effectiveness. This study employs a green self-activation method to synthesize a hybrid magnetic porous carbon composite, decorated with Fe<sub>3</sub>O<sub>4</sub>, ZnO, and ZnS (PZZF), aimed at the degradation of Rhodamine B. A variety of characterization techniques were employed in this study, including XRD, nitrogen adsorption-desorption analysis, FESEM, FTIR, HRTEM, Zeta potential, Raman spectroscopy, contact angle measurements, DRS, Mott-Schottky analysis, and VSM. HRTEM confirmed the successful formation of heterojunction structures with the desired chemical compositions. The specific surface area of the synthesized material was measured to be 313 m<sup>2</sup>.g<sup>−1</sup>, and the saturation magnetization was found to be 13.51 emu.g<sup>−1</sup>. The investigation of PZZF's photocatalytic activity against Rhodamine B highlights its enhanced efficiency, particularly under UV/H<sub>2</sub>O<sub>2</sub> treatment, leading to complete degradation of the dye within 60 min. Several factors affecting the degradation process were explored, including pH, catalyst dosage, H<sub>2</sub>O<sub>2</sub> concentration, and scavenger studies, providing comprehensive insight into the optimal conditions for maximum photocatalytic performance. The results from the radical trapping experiments demonstrated that hydroxyl radicals played a critical role in the degradation of Rhodamine B. Additionally, the total organic carbon (TOC) analysis showed that more than 96 % of the carbon in the RhB solution was effectively mineralized into CO<sub>2</sub> after 90 min of UV irradiation. DFT calculation results were aligned with experimental findings to validate theoretical predictions and enhance the overall understanding of the adsorption process. Ultimately, the UMAP technique was employed to visualize RhB adsorption and degradation by clustering and screening various configurations of the photocatalyst. These findings confirm the strong potential of the PZZF photocatalyst for effective dye degradation, highlighting its promising application in environmental remediation.</div></div>","PeriodicalId":22097,"journal":{"name":"Sustainable Materials and Technologies","volume":"43 ","pages":"Article e01231"},"PeriodicalIF":8.6,"publicationDate":"2024-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143137378","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sustainable high-density polyethylene/ferronickel slag composites for material extrusion additive manufacturing: Engineering, morphological, rheological, thermal, and chemical aspects
IF 8.6 2区 工程技术 Q1 ENERGY & FUELS Pub Date : 2024-12-30 DOI: 10.1016/j.susmat.2024.e01227
Markos Petousis , Dimitrios Kalderis , Nikolaos Michailidis , Vassilis Papadakis , Nikolaos Mountakis , Apostolos Argyros , Mariza Spiridaki , Constantine David , Dimitrios Sagris , Nectarios Vidakis
The increasing production of solid waste and the lack of valorization options for some of them pose a constant environmental threat. Ferronickel slag (FNS) is a solid waste derived from the smelting of ferronickel alloys and has a low utilization rate worldwide. In this study, FNS was used as an additive for high-density polyethylene (HDPE) thermoplastics. Six composites were produced, with FNS contents ranging from 2.0 to 14 wt%. The HDPE/FNS filaments were extruded and employed to manufacture 3D-printed parts using the material extrusion process. The filament and specimen samples were tested for their rheological, thermal, mechanical, and structural properties. The tensile, flexural, microhardness and Charpy impact mechanical properties of the composites were investigated. Scanning electron microscopy and energy-dispersive X-ray spectroscopy were performed. The highest mechanical performance was observed for HDPE/10.0 wt% FNS, in relation to the unfilled HDPE thermoplastic. All the mechanical properties were improved by more than 20 % at this loading. Such composites increase the mechanical response of HDPE thermoplastics in 3D printing and provide novel valorization routes for industrial waste, thus contributing to the circular economy and sustainability of the process.
{"title":"Sustainable high-density polyethylene/ferronickel slag composites for material extrusion additive manufacturing: Engineering, morphological, rheological, thermal, and chemical aspects","authors":"Markos Petousis ,&nbsp;Dimitrios Kalderis ,&nbsp;Nikolaos Michailidis ,&nbsp;Vassilis Papadakis ,&nbsp;Nikolaos Mountakis ,&nbsp;Apostolos Argyros ,&nbsp;Mariza Spiridaki ,&nbsp;Constantine David ,&nbsp;Dimitrios Sagris ,&nbsp;Nectarios Vidakis","doi":"10.1016/j.susmat.2024.e01227","DOIUrl":"10.1016/j.susmat.2024.e01227","url":null,"abstract":"<div><div>The increasing production of solid waste and the lack of valorization options for some of them pose a constant environmental threat. Ferronickel slag (FNS) is a solid waste derived from the smelting of ferronickel alloys and has a low utilization rate worldwide. In this study, FNS was used as an additive for high-density polyethylene (HDPE) thermoplastics. Six composites were produced, with FNS contents ranging from 2.0 to 14 wt%. The HDPE/FNS filaments were extruded and employed to manufacture 3D-printed parts using the material extrusion process. The filament and specimen samples were tested for their rheological, thermal, mechanical, and structural properties. The tensile, flexural, microhardness and Charpy impact mechanical properties of the composites were investigated. Scanning electron microscopy and energy-dispersive X-ray spectroscopy were performed. The highest mechanical performance was observed for HDPE/10.0 wt% FNS, in relation to the unfilled HDPE thermoplastic. All the mechanical properties were improved by more than 20 % at this loading. Such composites increase the mechanical response of HDPE thermoplastics in 3D printing and provide novel valorization routes for industrial waste, thus contributing to the circular economy and sustainability of the process.</div></div>","PeriodicalId":22097,"journal":{"name":"Sustainable Materials and Technologies","volume":"43 ","pages":"Article e01227"},"PeriodicalIF":8.6,"publicationDate":"2024-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143137374","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Sustainable Materials and Technologies
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