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Steering Mg anodic dissolution and hydrogen evolution via the interfacial double layer 通过界面双层控制Mg的阳极溶解和析氢
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-01-03 DOI: 10.1016/j.matlet.2026.140046
Jianlei Song , Lifeng Hou , Hongxia Zhang , Qixin Yan , Yinghui Wei
This study investigated the effect of sodium phosphate (Na₃PO₄) in NaCl solution on the polarization of magnesium (Mg) anode and the cathode hydrogen evolution. Na₃PO₄ demonstrates favorable sustained-release characteristics on magnesium corrosion, suppressing it in NaCl solution by reducing both hydrogen evolution rate and anodic dissolution. The established double-layer model at the Mg surface reveals the underlying inhibition/acceleration mechanisms, the dissolution rate and hydrogen evolution rate on the magnesium surface are governed by the coverage of its active sites.
研究了NaCl溶液中磷酸钠(Na₃PO₄)对镁(Mg)阳极极化和阴极析氢的影响。Na₃PO₄在NaCl溶液中表现出良好的缓释特性,通过降低析氢速率和阳极溶解来抑制镁的腐蚀。在Mg表面建立的双层模型揭示了潜在的抑制/加速机制,镁表面的溶解速率和析氢速率受其活性位点的覆盖范围的控制。
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引用次数: 0
Novel brine sludge/natural rubber composite reinforced with barium-bismuth oxide for X-ray radiation shielding in medical applications 新型卤水污泥/天然橡胶复合材料增强钡铋氧化物在x射线辐射屏蔽医疗应用
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-01-03 DOI: 10.1016/j.matlet.2026.140049
Sriparna Paul , Kamna Chaturvedi , Sarika Verma
In recent years, the development of non-toxic, lightweight, flexible and high performance X-Ray shielding material has shown a great concern amongst the researchers. The conventional flexible composites often leads to non-uniform attenuation behaviour due to the non-uniform distribution of fillers in the natural rubber matrix. In this work, efforts were made to address this limitation by fabricating a lead-free chemically bonded flexible sheets using brine sludge as a filler in a natural rubber matrix along with the curing agents to overcome the insufficient strength of the samples found in other reports. Designed with a uniform thickness of 2 mm and 5 mm, the composite materials were fabricated using a conventional two-roll milling under specific working conditions. The composites underwent thorough mixing, curing, and post-curing processes before being evaluated for their physical morphology, radiation shielding efficiency, and mechanical performance. X-ray shielding properties including linear attenuation coefficient (μ), mass attenuation coefficient (μm), and half value layer (HVL) have also been studied. It is seen that 5 mm thick composite exhibited superior shielding efficiency as compared to 2 mm thick composite and also offers 0.25 mm lead attenuation equivalent at 100 kV, aligning with International Atomic Energy Agency (IAEA) Standards and toxicity safety standards. These findings emphasize its potential for diverse medical and industrial uses as flexible radiation shielding materials in addition to their low cost, uniform attenuation throughout the matrix and contributions to a cleaner environment, with further research needed to enhance its shielding efficiency.
近年来,开发无毒、轻量、柔性、高性能的x射线屏蔽材料已成为研究人员关注的热点。由于填料在天然橡胶基体中的分布不均匀,导致传统柔性复合材料的衰减行为不均匀。在这项工作中,通过在天然橡胶基质中使用卤水污泥作为填料以及固化剂来制造无铅化学粘合柔性片,努力解决这一限制,以克服其他报告中发现的样品强度不足的问题。设计了厚度为2 mm和5 mm的复合材料,在特定的工作条件下,采用传统的双辊铣削工艺制备复合材料。复合材料经过了彻底的混合、固化和后固化过程,然后对其物理形态、辐射屏蔽效率和机械性能进行了评估。研究了线性衰减系数(μ)、质量衰减系数(μm)和半值层(HVL)等x射线屏蔽性能。与2毫米厚的复合材料相比,5毫米厚的复合材料表现出更好的屏蔽效率,并且在100千伏时也提供0.25毫米的等效铅衰减,符合国际原子能机构(IAEA)标准和毒性安全标准。这些发现强调了其作为柔性辐射屏蔽材料的多种医疗和工业用途的潜力,除了其成本低,在整个基质中均匀衰减以及对更清洁的环境做出贡献之外,还需要进一步研究以提高其屏蔽效率。
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引用次数: 0
Deformation twinning induced ultra-fine carbide precipitation in a newly developed austenitic stainless steel 新研制的奥氏体不锈钢变形孪晶析出超细碳化物
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-01-03 DOI: 10.1016/j.matlet.2026.140048
Yuefeng Jiang, Meiqiong Ou, Yaqian Yang, Min Wang, Yingche Ma
A novel austenitic stainless steel with a Ti/C ratio of 4 was recently designed for lead-cooled fast reactors. During the 450 °C long-term annealing, the 20 % cold-worked material with this specific Ti/C ratio exhibited dense precipitation within deformation twinning regions with the size predominantly below 100 nm. This unique behavior was synergistically promoted by the pre-existing twin boundaries, which provided abundant nucleation sites, and resulted in a remarkable increase in room-temperature tensile yield strength. In this paper, the cold-worked and thermally aged microstructures were characterized, and the precipitation mechanism governed by Ti/C stoichiometry and the resultant strengthening effects were discussed.
一种Ti/C比为4的新型奥氏体不锈钢最近被设计用于铅冷快堆。在450°C长期退火过程中,具有此特定Ti/C比的20%冷加工材料在变形孪晶区出现了密集的析出,且尺寸主要小于100 nm。这种独特的行为是由先前存在的孪晶界协同促进的,它提供了丰富的成核位点,并导致室温拉伸屈服强度的显著提高。本文对冷加工和热时效的显微组织进行了表征,并讨论了Ti/C化学计量学控制的析出机理和由此产生的强化效果。
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引用次数: 0
Delamination of selenium by wet media milling 湿介质铣削硒的分层
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-01-02 DOI: 10.1016/j.matlet.2025.140042
Z. Lukáčová Bujňáková , O. Shpotyuk , M. Baláž , J. Briančin , K. Hreus , L. Storozhuk , E. Dutková
The successful delamination of bulk selenium (Se) into a 2D-structured selenene was first achieved through a two-step mechanochemical processing. In the first step, the powdered bulk Se was co-milled in a planetary mill with sodium chloride NaCl acting as a solid solvent, essentially reducing the crystallite sizes (from 36 nm to 26 nm) and microstrain of trigonal Se. This NaCl-assisted pre-milling is necessary for further successful delamination of nanostructured Se. In the second step, the delamination of pre-milled Se was carried out using wet media milling in a polyvinylpyrrolidone solution. As a result, sheets of 2D-structured Se, composed of one or several layers with a 183-times increased specific surface area compared to the starting samples (from 0.06 m2/g to 11 m2/g), were fabricated. The sample characteristics were evaluated using X-ray diffraction analysis, scanning and transmission microscopy, and specific surface area measurements.
通过两步机械化学处理,成功地将大块硒(Se)分层成二维结构的硒烯。在第一步中,以氯化钠NaCl作为固体溶剂,在行星磨机中共磨块状Se粉末,从根本上减少了三角形Se的晶粒尺寸(从36 nm降至26 nm)和微应变。这种nacl辅助的预磨对于进一步成功地分层纳米结构硒是必要的。第二步,采用湿介质在聚乙烯吡咯烷酮溶液中对预磨好的Se进行分层。结果,制备出了由一层或多层组成的二维结构硒片,比表面积比开始样品(从0.06 m2/g增加到11 m2/g)增加了183倍。使用x射线衍射分析、扫描和透射显微镜以及比表面积测量来评估样品的特性。
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引用次数: 0
Grain refinement and ferrite-selective texturing in duplex stainless steel 2205 induced by severe shot peening 双相不锈钢2205剧烈喷丸强化引起的晶粒细化和铁素体选择性织构
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-01-02 DOI: 10.1016/j.matlet.2026.140043
Yee Ng, Tzee Luai Meng, Xian Yi Tan, Coryl J.J. Lee, Chee Kiang Ivan Tan, Dennis C.C. Tan, Hongfei Liu
Severe shot peening (SSP) was applied to DSS2205 duplex stainless steel at an intensity of 0.635 mmA with coverages of 100–1500 %. Crystallographic evolution was characterized by X-ray diffraction and electron backscatter diffraction. Both phases exhibited near-surface grain refinement, with more pronounced refinement in austenite, while no austenite-to-martensite transformation was detected. In contrast to austenite, ferrite developed strong texture through rotation of the [111] axis towards the surface normal. These structural modifications were confined to a ∼ 200 μm layer, increased with coverage, and saturated at ∼1000 %. Differences between phases are attributed to distinct plastic deformation mechanisms.
对DSS2205双相不锈钢进行了强度为0.635 mmA的强力喷丸强化处理(SSP),喷丸强度为100 - 1500%。用x射线衍射和电子背散射衍射对晶体演化进行了表征。两相均表现出近表面晶粒细化,其中奥氏体细化更为明显,而未见奥氏体向马氏体转变。与奥氏体相反,铁素体通过向表面法向旋转[111]轴而形成了强大的织构。这些结构修饰被限制在~ 200 μm的层内,随着覆盖范围的增加而增加,并在~ 1000%饱和。不同相之间的差异归因于不同的塑性变形机制。
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引用次数: 0
Achieving high strength and ductility in rapidly solidified Al-Mg-Li alloy via heat treatment 通过热处理实现快速凝固Al-Mg-Li合金的高强度和高延展性
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-01-02 DOI: 10.1016/j.matlet.2026.140044
Quanbo Kuang , Richu Wang , Juangang Zhao
The microstructure evolution and mechanical properties of a rapidly solidified Al-Mg-Li alloy under different aging conditions were investigated. The results showed that Al3Li is the primary precipitated phases in the alloy after aging treatment. Higher aging temperature and dislocations induced by pre-deformation accelerated the coarsening of Al3Li. An outstanding yield strength of 418 ± 5 MPa, ultimate tensile strength of 546 ± 7 MPa, and elongation of 12.8 ± 0.5 % were obtained in the pre-deformation aging alloy. The increased strength is attributed to the homogeneous distribution of fine Al3Li phase combined with dislocation strengthening.
研究了Al-Mg-Li快速凝固合金在不同时效条件下的组织演变和力学性能。结果表明:时效处理后合金中主要析出相为Al3Li;较高的时效温度和预变形引起的位错加速了Al3Li的粗化。预变形时效合金的屈服强度为418±5 MPa,极限抗拉强度为546±7 MPa,伸长率为12.8±0.5%。强度的提高主要是由于Al3Li相的均匀分布和位错强化。
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引用次数: 0
Hierarchical urchin-shaped TiO2@C-Si@C nanocomposite: Facile synthesis and structural design toward lithium-ion battery anodes 层叠海胆形状TiO2@C-Si@C纳米复合材料:锂离子电池阳极的简易合成和结构设计
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-01-02 DOI: 10.1016/j.matlet.2025.140032
Van Hau Tran , Tien Dung Cao , Thi Huyen Nguyen , Van Trinh Pham , Van Chuc Nguyen , Thi Thanh Cao , Hung Thang Bui , Thi Nam Pham , Hoang Tung Nguyen , Duy Long Pham , Thanh Tung Nguyen , Dai Lam Tran , Ngoc Minh Phan , Van Hao Nguyen , Van Tu Nguyen
In this study, we report on novel anode material based on hierarchical urchin-shaped TiO2@C-Si@C (u-TSC) nanocomposite. To form the nanocomposite, urchin-shaped TiO2 was first prepared through a hydrothermal process and then used as a framework for decorating sodium deoxycholate (SDC)-assisted silicon nanoparticles (SiNPs), followed by thermal annealing at 800C in argon gas. The obtained results showed a good distribution of SiNPs on the TiO2 nanoneedles. The u-TSC nanocomposite anode showed an initial discharge/charge capacity of 715/354 mAhg−1 at a current density of 100 mAg−1 and retained discharge capacity of 458 mAhg−1 after 100 cycles, which was attributed to the synergistic effects of TiO2 framework, conductive carbon layer, and SiNPs. These findings open a promising strategy for the development of high-performance anode materials based on TiO2 and Si for lithium-ion batteries (LIBs).
在这项研究中,我们报道了基于层叠海胆形状TiO2@C-Si@C (u-TSC)纳米复合材料的新型阳极材料。为了形成纳米复合材料,首先通过水热法制备海胆形状的TiO2,然后将其作为修饰脱氧胆酸钠(SDC)辅助硅纳米粒子(SiNPs)的框架,然后在800℃氩气中进行热退火。结果表明,SiNPs在TiO2纳米针尖上分布良好。在电流密度为100 mAg−1时,u-TSC纳米复合阳极的初始放电/充电容量为715/354 mAhg−1,循环100次后仍保持458 mAhg−1的放电容量,这是TiO2框架、导电碳层和sinp的协同作用的结果。这些发现为开发基于TiO2和Si的高性能锂离子电池负极材料开辟了一条有希望的策略。
{"title":"Hierarchical urchin-shaped TiO2@C-Si@C nanocomposite: Facile synthesis and structural design toward lithium-ion battery anodes","authors":"Van Hau Tran ,&nbsp;Tien Dung Cao ,&nbsp;Thi Huyen Nguyen ,&nbsp;Van Trinh Pham ,&nbsp;Van Chuc Nguyen ,&nbsp;Thi Thanh Cao ,&nbsp;Hung Thang Bui ,&nbsp;Thi Nam Pham ,&nbsp;Hoang Tung Nguyen ,&nbsp;Duy Long Pham ,&nbsp;Thanh Tung Nguyen ,&nbsp;Dai Lam Tran ,&nbsp;Ngoc Minh Phan ,&nbsp;Van Hao Nguyen ,&nbsp;Van Tu Nguyen","doi":"10.1016/j.matlet.2025.140032","DOIUrl":"10.1016/j.matlet.2025.140032","url":null,"abstract":"<div><div>In this study, we report on novel anode material based on hierarchical urchin-shaped TiO<sub>2</sub>@C-Si@C (u-TSC) nanocomposite. To form the nanocomposite, urchin-shaped TiO<sub>2</sub> was first prepared through a hydrothermal process and then used as a framework for decorating sodium deoxycholate (SDC)-assisted silicon nanoparticles (SiNPs), followed by thermal annealing at 800C in argon gas. The obtained results showed a good distribution of SiNPs on the TiO<sub>2</sub> nanoneedles. The u-TSC nanocomposite anode showed an initial discharge/charge capacity of 715/354 mAhg<sup>−1</sup> at a current density of 100 mAg<sup>−1</sup> and retained discharge capacity of 458 mAhg<sup>−1</sup> after 100 cycles, which was attributed to the synergistic effects of TiO<sub>2</sub> framework, conductive carbon layer, and SiNPs. These findings open a promising strategy for the development of high-performance anode materials based on TiO<sub>2</sub> and Si for lithium-ion batteries (LIBs).</div></div>","PeriodicalId":384,"journal":{"name":"Materials Letters","volume":"407 ","pages":"Article 140032"},"PeriodicalIF":2.7,"publicationDate":"2026-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145922577","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Photoelectrically tunable CZTS-based memristors for bio-synaptic plasticity emulation 生物突触可塑性仿真的光电可调czts记忆电阻器
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-01-02 DOI: 10.1016/j.matlet.2026.140045
Siyuan Li, Fengxia Yang, Hao Sun, Xiaofei Dong, Yan Li
Photo-tunable synaptic memristors are crucial for breaking the von Neumann bottleneck and advancing neuromorphic computing; however, there are still challenges, and further in-depth exploration is needed. In this study, Cu2ZnSnS4 (CZTS) is employed as the resistive switching material to fabricate synaptic memristors with an Al/CZTS/FTO architecture. Their resistive switching performance and emulation of biological synaptic plasticity under photoelectric stimulation are systematically investigated. Experimental results demonstrate that the device exhibits stable bipolar resistive switching behavior, with its On/Off ratio tunable by adjusting the thickness of the CZTS switching layer. Mechanistic analysis reveals that the resistive switching originates from the formation and rupture of conductive filaments mediated by Cu+ migration. Moreover, under light and electrical pulse stimulation, the device well emulates key biological synaptic behaviors, including long-term potentiation (LTP), long-term depression (LTD), and brain-inspired “learning-forgetting-consolidation” behavior. These findings hold significant implications for the development of computing systems that regulate neuromorphic functions through the coupling of photoelectric signals.
光可调谐突触记忆电阻器对于打破冯·诺伊曼瓶颈和推进神经形态计算至关重要;但仍存在挑战,需要进一步深入探索。本研究采用Cu2ZnSnS4 (CZTS)作为阻性开关材料,制作Al/CZTS/FTO结构的突触忆阻器。系统地研究了它们的电阻开关性能和光电刺激下生物突触可塑性的模拟。实验结果表明,该器件表现出稳定的双极电阻开关行为,其开关比可通过调节CZTS开关层的厚度来调节。机理分析表明,电阻开关源于Cu+迁移介导导电丝的形成和断裂。此外,在光脉冲和电脉冲刺激下,该装置可以很好地模拟关键的生物突触行为,包括长期增强(LTP)、长期抑制(LTD)和大脑激发的“学习-遗忘-巩固”行为。这些发现对于通过光电信号耦合来调节神经形态功能的计算系统的发展具有重要意义。
{"title":"Photoelectrically tunable CZTS-based memristors for bio-synaptic plasticity emulation","authors":"Siyuan Li,&nbsp;Fengxia Yang,&nbsp;Hao Sun,&nbsp;Xiaofei Dong,&nbsp;Yan Li","doi":"10.1016/j.matlet.2026.140045","DOIUrl":"10.1016/j.matlet.2026.140045","url":null,"abstract":"<div><div>Photo-tunable synaptic memristors are crucial for breaking the von Neumann bottleneck and advancing neuromorphic computing; however, there are still challenges, and further in-depth exploration is needed. In this study, Cu<sub>2</sub>ZnSnS<sub>4</sub> (CZTS) is employed as the resistive switching material to fabricate synaptic memristors with an Al/CZTS/FTO architecture. Their resistive switching performance and emulation of biological synaptic plasticity under photoelectric stimulation are systematically investigated. Experimental results demonstrate that the device exhibits stable bipolar resistive switching behavior, with its On/Off ratio tunable by adjusting the thickness of the CZTS switching layer. Mechanistic analysis reveals that the resistive switching originates from the formation and rupture of conductive filaments mediated by Cu<sup>+</sup> migration. Moreover, under light and electrical pulse stimulation, the device well emulates key biological synaptic behaviors, including long-term potentiation (LTP), long-term depression (LTD), and brain-inspired “learning-forgetting-consolidation” behavior. These findings hold significant implications for the development of computing systems that regulate neuromorphic functions through the coupling of photoelectric signals.</div></div>","PeriodicalId":384,"journal":{"name":"Materials Letters","volume":"407 ","pages":"Article 140045"},"PeriodicalIF":2.7,"publicationDate":"2026-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145922490","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Two-step synthesis of porous SnO2 nanowall film via chemical bath deposition and post-oxidation 化学浴沉积-后氧化两步法制备多孔SnO2纳米膜
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-01-01 DOI: 10.1016/j.matlet.2025.140029
Lingsheng Chen, Yajie Zhang, Xin Jin
In recent years, with the rise of research on solar cells, tin oxide (SnO2) has been increasingly widely used as an electron transporting layer material (ETL). However, the conventional planar SnO2 films prepared by existing spin-coating processes suffer from non-negligible low carrier transport efficiency due to their limited contact area with the photoactive layer. To address this issue, here we propose for the first time a two-step strategy based on chemical bath deposition (CBD) to prepare high-quality porous SnO2 nanowall film, which is experimentally demonstrated to possess an open channel structure with excellent filling capability. The key advantage of our strategy lies in its capability to dramatically increase the interfacial contact area between the ETL and the photoactive layer. This enhanced interface provides a viable route to optimize carrier transport and thus boost solar cell efficiency.
近年来,随着太阳能电池研究的兴起,氧化锡(SnO2)作为电子传输层材料(ETL)得到了越来越广泛的应用。然而,现有的旋转镀膜工艺制备的传统平面SnO2薄膜由于与光活性层的接触面积有限,导致载流子输运效率低,不可忽略。为了解决这一问题,本文首次提出了一种基于化学浴沉积(CBD)的两步策略来制备高质量的多孔SnO2纳米壁膜,实验证明该膜具有开放通道结构和优异的填充能力。我们的策略的关键优势在于它能够显着增加ETL和光活性层之间的界面接触面积。这种增强的界面为优化载流子传输提供了可行的途径,从而提高了太阳能电池的效率。
{"title":"Two-step synthesis of porous SnO2 nanowall film via chemical bath deposition and post-oxidation","authors":"Lingsheng Chen,&nbsp;Yajie Zhang,&nbsp;Xin Jin","doi":"10.1016/j.matlet.2025.140029","DOIUrl":"10.1016/j.matlet.2025.140029","url":null,"abstract":"<div><div>In recent years, with the rise of research on solar cells, tin oxide (SnO<sub>2</sub>) has been increasingly widely used as an electron transporting layer material (ETL). However, the conventional planar SnO<sub>2</sub> films prepared by existing spin-coating processes suffer from non-negligible low carrier transport efficiency due to their limited contact area with the photoactive layer. To address this issue, here we propose for the first time a two-step strategy based on chemical bath deposition (CBD) to prepare high-quality porous SnO<sub>2</sub> nanowall film, which is experimentally demonstrated to possess an open channel structure with excellent filling capability. The key advantage of our strategy lies in its capability to dramatically increase the interfacial contact area between the ETL and the photoactive layer. This enhanced interface provides a viable route to optimize carrier transport and thus boost solar cell efficiency.</div></div>","PeriodicalId":384,"journal":{"name":"Materials Letters","volume":"407 ","pages":"Article 140029"},"PeriodicalIF":2.7,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145882914","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
A single-step, solvent-free synthesis of di-2-ethylhexyl oxalate plasticizer as an alternative to toxic phthalate plasticizers for PVC gel-based soft robots 单步、无溶剂合成草酸二乙基己酯增塑剂,作为PVC凝胶型软机器人中邻苯二甲酸酯增塑剂的替代品
IF 2.7 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-12-31 DOI: 10.1016/j.matlet.2025.140034
Gouri Tudu , Ganesh Pattan-Siddappa , Seok-Han Lee, Sang-Youn Kim
Phthalate plasticizers are the most commonly employed to plasticize PVC, however they are recognized to be hazardous to both the environment and human health. In order to develop an environmentally friendly plasticizer for PVC gels, we synthesized a non-phthalate plasticizer di-2-ethylhexyl oxalate (DEHO) and demonstrated its efficient plasticizing properties against PVC, followed by a structural and mechanical analysis. Furthermore, the properties were compared to commercially available PVC plasticizers. The observed percent transmittance (% T) of PVC-DEHO was 87 %, which was higher than PVC-DBP (57 %), PVC-ATBC (81 %), and comparable to PVC-DBA (89 %). Interestingly, PVC gel prepared with DEHO plasticizer has a higher percentage strain (∼250) than the gel prepared with commercially available ATBC plasticizer (∼182). Further, a bending actuator fabricated with PVC-DEHO exhibited bending angle of 10° and 20°, at input voltage of 0.5 kV and 1 kV respectively. The experimental results indicate that DEHO can successfully act as a plasticizer for PVC.
邻苯二甲酸酯增塑剂是最常用的PVC增塑剂,但它们被认为对环境和人体健康都有害。为了开发一种环保型PVC凝胶增塑剂,我们合成了一种非邻苯二甲酸酯类增塑剂二-2-乙基己基草酸酯(DEHO),并对其进行了结构和力学分析,证明了其对PVC的高效增塑剂。此外,还将其性能与市售的PVC增塑剂进行了比较。观察到PVC-DEHO的透光率(% T)为87%,高于PVC-DBP(57%)、PVC-ATBC(81%),与PVC-DBA(89%)相当。有趣的是,用DEHO增塑剂制备的PVC凝胶比用市售的ATBC增塑剂(~ 182)制备的凝胶具有更高的应变百分比(~ 250)。此外,在0.5 kV和1 kV输入电压下,用PVC-DEHO制成的弯曲致动器弯曲角度分别为10°和20°。实验结果表明,DEHO可以成功地作为PVC的增塑剂。
{"title":"A single-step, solvent-free synthesis of di-2-ethylhexyl oxalate plasticizer as an alternative to toxic phthalate plasticizers for PVC gel-based soft robots","authors":"Gouri Tudu ,&nbsp;Ganesh Pattan-Siddappa ,&nbsp;Seok-Han Lee,&nbsp;Sang-Youn Kim","doi":"10.1016/j.matlet.2025.140034","DOIUrl":"10.1016/j.matlet.2025.140034","url":null,"abstract":"<div><div>Phthalate plasticizers are the most commonly employed to plasticize PVC, however they are recognized to be hazardous to both the environment and human health. In order to develop an environmentally friendly plasticizer for PVC gels, we synthesized a non-phthalate plasticizer di-2-ethylhexyl oxalate (DEHO) and demonstrated its efficient plasticizing properties against PVC, followed by a structural and mechanical analysis. Furthermore, the properties were compared to commercially available PVC plasticizers. The observed percent transmittance (% T) of PVC-DEHO was 87 %, which was higher than PVC-DBP (57 %), PVC-ATBC (81 %), and comparable to PVC-DBA (89 %). Interestingly, PVC gel prepared with DEHO plasticizer has a higher percentage strain (∼250) than the gel prepared with commercially available ATBC plasticizer (∼182). Further, a bending actuator fabricated with PVC-DEHO exhibited bending angle of 10° and 20°, at input voltage of 0.5 kV and 1 kV respectively. The experimental results indicate that DEHO can successfully act as a plasticizer for PVC.</div></div>","PeriodicalId":384,"journal":{"name":"Materials Letters","volume":"407 ","pages":"Article 140034"},"PeriodicalIF":2.7,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145922572","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
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