首页 > 最新文献

RAN最新文献

英文 中文
Photocatalytic Activity of Er-TiO2 Nanocomposite Er-TiO2纳米复合材料的光催化活性
RAN
Pub Date : 2017-04-01 DOI: 10.11159/ICNMS17.106
E. Wyrzykowska, A. Mikołajczyk, Joanna Nadolna, T. Puzyn
Extended Abstract One of the directions in the evolution of the environmental friendly technologies is developing efficient methods of contaminant disposal. Particularly, researchers pay attention to the semiconductor-based heterogeneous photocatalysis that plays a crucial role in degradation of impurities in the presence of TiO2 nanomaterials. At present, the methods based on photodegradation are widely used during purifications of water streams and wastewater, as well as to remove volatile substances from the atmosphere. This approach uses commonly available resources of solar radiation and simultaneously does not require additional chemicals during purification, what is a huge advantage over any other conventional methods. The photocatalytic property of TiO2 is closely related with the band gap energy. When the semiconductor (TiO2) is exposure on the solar radiation, the photon hv with the energy equal or greater than the band gap of TiO2 (~3.2 eV) creates electron-hole pair – the valence electron is excited and promoted to conduction band, while the positive hole is formed on the valence band. This metastable state can be recombine and release the energy as a heat or in reaction with surrounding electron donors/acceptors (causing their degradation at the same time) or as a result of interactions with the surrounding double layer of the particle. The minimum energy to performed electron–hole pair (~3.2 eV) corresponds to the photon energy at a wavelength of λ>388 nm, what is 3-5% of solar radiation. The main drawback of application of TiO2 NPs as environmentally benign treatment technology for a variety of pollutants is that it can only be excited by ultraviolet light. Thus, an extension of its absorption wavelength range to the visible region (vis) is desirable to use the main part of solar spectrum. One of the most promising approach for extension of the spectral sensitivity is to influence electronic properties of TiO2 by some structure modifications. In this way, it is possible to get an efficient photocatalyst activated of UV, Vis and NIR radiation. Reactivity of TiO2 in visible light (λ> 400 nm) can be achieved by: (i) transition metal ions doping (e.g. Cr, Mn, Mo, Nb, V, Fe, Ru, Au), (ii) non-metals doping (e.g. N, S, B, F, I), (iii) reduced form of TiO2-x, or (iv) doping with semiconductors, which have lower band gap energy. Recently, researchers provide potentials for TiO2 photocatalysts modified lanthanides, for example holmium atom [1]. The modified titanium dioxide nanomaterial can form the basis for the new generation semiconductor. The aim of the project is to develop the TiO2-based semiconductor having photocatalytic activity under visible (λ>380 nm) and NIR (λ>780 nm) radiation. This study has demonstrated application of the plane-wave-based Vienna ab-initio simulation package (VASP) to obtain predictive knowledge on structural features of RE-TiO2 nanoparticles (RE rare earth metal) that may govern their photocatalytic activity
发展高效的污染物处理方法是环境友好技术发展的方向之一。特别是,研究人员关注了基于半导体的多相光催化,它在TiO2纳米材料存在下对杂质的降解起着至关重要的作用。目前,基于光降解的方法被广泛应用于水流和废水的净化以及大气中挥发性物质的去除。这种方法利用了常见的太阳辐射资源,同时在净化过程中不需要额外的化学物质,这是任何其他传统方法都无法比拟的巨大优势。TiO2的光催化性能与带隙能密切相关。当半导体(TiO2)暴露在太阳辐射下时,能量等于或大于TiO2带隙的光子hv (~3.2 eV)产生电子-空穴对,价电子被激发并提升到导带,而价带上形成正空穴。这种亚稳态可以重新组合并释放能量,作为热量或与周围的电子供体/受体反应(同时引起它们的降解),或作为与周围的双层粒子相互作用的结果。产生的电子-空穴对的最小能量(~3.2 eV)对应于波长为λ>388 nm的光子能量,相当于太阳辐射的3-5%。TiO2 NPs作为环境友好型处理多种污染物的技术,其主要缺点是只能由紫外光激发。因此,为了利用太阳光谱的主要部分,需要将其吸收波长范围扩展到可见区域(vis)。提高TiO2的光谱灵敏度最有希望的方法之一是通过一些结构修饰来影响TiO2的电子性质。这样,就有可能得到一种具有紫外、可见和近红外活性的高效光催化剂。TiO2在可见光(λ> 400 nm)下的反应性可以通过:(i)过渡金属离子掺杂(如Cr, Mn, Mo, Nb, V, Fe, Ru, Au), (ii)非金属掺杂(如N, S, B, F, i), (iii) TiO2-x的还原形式,或(iv)与带隙能量较低的半导体掺杂来实现。最近,研究人员提出了二氧化钛光催化剂修饰镧系元素的潜力,例如钬原子[1]。改性后的二氧化钛纳米材料可为新一代半导体材料奠定基础。该项目的目标是开发在可见光(λ>380 nm)和近红外(λ>780 nm)辐射下具有光催化活性的二氧化钛基半导体。本研究展示了基于平面波的Vienna ab-initio模拟包(VASP)的应用,以获得可能影响其光催化活性的RE- tio2纳米颗粒(RE稀土金属)结构特征的预测知识。本研究的主要目的是建立含有铒的表面修饰TiO2纳米粒子(Er-TiO2)的分子模型,用于描述表面修饰TiO2基体系的Er结构与电子性能之间的关系。了解Er对TiO2光催化活性的影响有助于未来新一代半导体的设计。
{"title":"Photocatalytic Activity of Er-TiO2 Nanocomposite","authors":"E. Wyrzykowska, A. Mikołajczyk, Joanna Nadolna, T. Puzyn","doi":"10.11159/ICNMS17.106","DOIUrl":"https://doi.org/10.11159/ICNMS17.106","url":null,"abstract":"Extended Abstract One of the directions in the evolution of the environmental friendly technologies is developing efficient methods of contaminant disposal. Particularly, researchers pay attention to the semiconductor-based heterogeneous photocatalysis that plays a crucial role in degradation of impurities in the presence of TiO2 nanomaterials. At present, the methods based on photodegradation are widely used during purifications of water streams and wastewater, as well as to remove volatile substances from the atmosphere. This approach uses commonly available resources of solar radiation and simultaneously does not require additional chemicals during purification, what is a huge advantage over any other conventional methods. The photocatalytic property of TiO2 is closely related with the band gap energy. When the semiconductor (TiO2) is exposure on the solar radiation, the photon hv with the energy equal or greater than the band gap of TiO2 (~3.2 eV) creates electron-hole pair – the valence electron is excited and promoted to conduction band, while the positive hole is formed on the valence band. This metastable state can be recombine and release the energy as a heat or in reaction with surrounding electron donors/acceptors (causing their degradation at the same time) or as a result of interactions with the surrounding double layer of the particle. The minimum energy to performed electron–hole pair (~3.2 eV) corresponds to the photon energy at a wavelength of λ>388 nm, what is 3-5% of solar radiation. The main drawback of application of TiO2 NPs as environmentally benign treatment technology for a variety of pollutants is that it can only be excited by ultraviolet light. Thus, an extension of its absorption wavelength range to the visible region (vis) is desirable to use the main part of solar spectrum. One of the most promising approach for extension of the spectral sensitivity is to influence electronic properties of TiO2 by some structure modifications. In this way, it is possible to get an efficient photocatalyst activated of UV, Vis and NIR radiation. Reactivity of TiO2 in visible light (λ> 400 nm) can be achieved by: (i) transition metal ions doping (e.g. Cr, Mn, Mo, Nb, V, Fe, Ru, Au), (ii) non-metals doping (e.g. N, S, B, F, I), (iii) reduced form of TiO2-x, or (iv) doping with semiconductors, which have lower band gap energy. Recently, researchers provide potentials for TiO2 photocatalysts modified lanthanides, for example holmium atom [1]. The modified titanium dioxide nanomaterial can form the basis for the new generation semiconductor. The aim of the project is to develop the TiO2-based semiconductor having photocatalytic activity under visible (λ>380 nm) and NIR (λ>780 nm) radiation. This study has demonstrated application of the plane-wave-based Vienna ab-initio simulation package (VASP) to obtain predictive knowledge on structural features of RE-TiO2 nanoparticles (RE rare earth metal) that may govern their photocatalytic activity","PeriodicalId":31009,"journal":{"name":"RAN","volume":"23 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88430719","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Redox Property of Cu-Fe Based Oxygen Carriers Promoted with MnO2 MnO2促进Cu-Fe基氧载体的氧化还原性能
RAN
Pub Date : 2017-04-01 DOI: 10.11159/ICNNFC17.113
Yong Han Jeong, N. Park, T. Lee, S. Ryu, Misook Kang, J. Baek, H. Ryu
Yong Han Jeong, No-Kuk Park, Tae Jin Lee, Si Ok Ryu, Misook Kang, Jeom-In Baek, Ho-Jung Ryu School of Chemical Engineering, Yeungnam University 280, Daehak-Ro, Gyeongsan, Korea madmovie0@gmail.com; nokukpark@ynu.ac.kr; soryu@ynu.ac.kr; tjlee@ynu.ac.kr School of Chemistry, Yeungnam University mskang@ynu.ac.kr Korea Electric Power Research Institute 105, Munji-Ro, Yuseong-Gu, Daejeon, Korea jibaek@kepco.co.kr Korea Institute Energy Research 152, Gajeong-Ro, Yuseong-Gu, Daejeon, Korea hjryu@kier.re.kr
韩国庆山大学路280,岭南大学化学工程学院madmovie0@gmail.com;nokukpark@ynu.ac.kr;soryu@ynu.ac.kr;tjlee@ynu.ac.kr岭南大学化学学院mskang@ynu.ac.kr韩国电力研究院105号(大田儒城区文知路)jibaek@kepco.co.kr韩国能源研究院152号(大田儒城区嘉正路)hjryu@kier.re.kr
{"title":"Redox Property of Cu-Fe Based Oxygen Carriers Promoted with MnO2","authors":"Yong Han Jeong, N. Park, T. Lee, S. Ryu, Misook Kang, J. Baek, H. Ryu","doi":"10.11159/ICNNFC17.113","DOIUrl":"https://doi.org/10.11159/ICNNFC17.113","url":null,"abstract":"Yong Han Jeong, No-Kuk Park, Tae Jin Lee, Si Ok Ryu, Misook Kang, Jeom-In Baek, Ho-Jung Ryu School of Chemical Engineering, Yeungnam University 280, Daehak-Ro, Gyeongsan, Korea madmovie0@gmail.com; nokukpark@ynu.ac.kr; soryu@ynu.ac.kr; tjlee@ynu.ac.kr School of Chemistry, Yeungnam University mskang@ynu.ac.kr Korea Electric Power Research Institute 105, Munji-Ro, Yuseong-Gu, Daejeon, Korea jibaek@kepco.co.kr Korea Institute Energy Research 152, Gajeong-Ro, Yuseong-Gu, Daejeon, Korea hjryu@kier.re.kr","PeriodicalId":31009,"journal":{"name":"RAN","volume":"4184 1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86778609","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Inorganic Ligand-Capped Colloidal Nanocrystals for Electronic Device Application 无机配体覆盖胶体纳米晶体在电子器件中的应用
RAN
Pub Date : 2017-04-01 DOI: 10.11159/icnnfc17.135
Jaeyoung Jang
Extended Abstract Colloidal nanocrystals can combine the advantages of crystalline inorganic semiconductors with the size-tunable electronic structure and inexpensive solution-based device fabrication.[1] They are of great interest due to these unique advantages for use in electronic and optoelectronic devices such as field-effect transistors (FETs), photovoltaic cells, and light-emitting diodes.[1-8] Efficient charge transport is crucial for high performance of nanocrystal-based electronic and optoelectronic devices.[2,3] Many practical implementations of nanocrystals are hindered by the poor electronic coupling in close-packed nanocrystal films, caused by the presence of bulky organic surface ligands. In this study, to address this fundamental problem, various types of inorganic surface ligands are introduced.[2,4,5] By using optimized inorganic surface ligands, nanocrystal solids are prepared exhibiting band-like charge transport, high photoconductivity and tunable doping level.[6] For example, we explore the temperature-dependent Hall effect of inorganically capped InAs nanocrystals. In addition, a solution-based “soldering” process is introduced to fabricate ultrahigh electron mobility (>300 cm 2 /Vs) nanocrystal solids using colloidal nanocrystals with molecular “solders”.[7,8] The high-mobility FETs were fabrcated by spin-coating a solution of Cd2Se3 2-capped CdSe nanocrystals, followed by thermal annealing. Finally, we expand the application of the NC soldering process to core−shell NCs consisting of a III−V InAs core and a CdSe shell with composition-matched Cd2Se3 2− molecular solders. Soldering CdSe shells forms nanoheterostructured material that combines high electron mobility and near-IR photoresponse.
胶体纳米晶体可以将晶体无机半导体的优点与尺寸可调的电子结构和廉价的基于溶液的器件制造相结合。[1]由于它们在电子和光电子器件(如场效应晶体管(fet)、光伏电池和发光二极管)中的独特优势,它们引起了人们的极大兴趣。[1-8]高效率的电荷输运对于纳米晶体电子和光电子器件的高性能至关重要。[2,3]由于存在体积庞大的有机表面配体,在致密的纳米晶体薄膜中电子耦合不良,阻碍了纳米晶体的许多实际实现。在本研究中,为了解决这一基本问题,介绍了各种类型的无机表面配体。[2,4,5]通过使用优化的无机表面配体,制备出具有带状电荷输运、高光导性和可调掺杂水平的纳米晶体固体[6]。例如,我们探索了无机覆盖的InAs纳米晶体的温度依赖霍尔效应。此外,还引入了一种基于溶液的“焊接”工艺,利用胶体纳米晶体和分子“焊料”制造超高电子迁移率(>300 cm 2 /Vs)的纳米晶体固体。[7,8]采用自旋涂覆Cd2Se3 - 2包覆CdSe纳米晶溶液的方法制备高迁移率场效应管,然后进行热退火。最后,我们将NC焊接工艺的应用扩展到由III−V InAs核心和CdSe外壳组成的芯壳NC,并使用成分匹配的cd2se32 -分子焊料。焊接CdSe壳形成纳米异质结构材料,结合了高电子迁移率和近红外光响应。
{"title":"Inorganic Ligand-Capped Colloidal Nanocrystals for Electronic Device Application","authors":"Jaeyoung Jang","doi":"10.11159/icnnfc17.135","DOIUrl":"https://doi.org/10.11159/icnnfc17.135","url":null,"abstract":"Extended Abstract Colloidal nanocrystals can combine the advantages of crystalline inorganic semiconductors with the size-tunable electronic structure and inexpensive solution-based device fabrication.[1] They are of great interest due to these unique advantages for use in electronic and optoelectronic devices such as field-effect transistors (FETs), photovoltaic cells, and light-emitting diodes.[1-8] Efficient charge transport is crucial for high performance of nanocrystal-based electronic and optoelectronic devices.[2,3] Many practical implementations of nanocrystals are hindered by the poor electronic coupling in close-packed nanocrystal films, caused by the presence of bulky organic surface ligands. In this study, to address this fundamental problem, various types of inorganic surface ligands are introduced.[2,4,5] By using optimized inorganic surface ligands, nanocrystal solids are prepared exhibiting band-like charge transport, high photoconductivity and tunable doping level.[6] For example, we explore the temperature-dependent Hall effect of inorganically capped InAs nanocrystals. In addition, a solution-based “soldering” process is introduced to fabricate ultrahigh electron mobility (>300 cm 2 /Vs) nanocrystal solids using colloidal nanocrystals with molecular “solders”.[7,8] The high-mobility FETs were fabrcated by spin-coating a solution of Cd2Se3 2-capped CdSe nanocrystals, followed by thermal annealing. Finally, we expand the application of the NC soldering process to core−shell NCs consisting of a III−V InAs core and a CdSe shell with composition-matched Cd2Se3 2− molecular solders. Soldering CdSe shells forms nanoheterostructured material that combines high electron mobility and near-IR photoresponse.","PeriodicalId":31009,"journal":{"name":"RAN","volume":"1 2 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78412104","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Fabrication Process for Nanopatterns Shrinkage with Variable Sizes for Large Area 一种大面积变尺寸收缩纳米图案的制备工艺
RAN
Pub Date : 2017-04-01 DOI: 10.11159/ICNNFC17.129
S. Si, Lars Dittrich, M. Hoffmann
In this paper, a cost efficient process chain is designed to shrink periodic nanopatterns to tunable feature sizes. The feature size of the final patterns can be controlled and adjusted. 100 mm full wafers featuring square holes with 130 nm, 160 nm, 190 nm and 220 nm feature sizes are fabricated from the original wafer containing circular holes with a diameter of 350 nm. The fabrication chain involves well-known technologies such as etching and soft UV nanoimprint lithography (UV-NIL). Based on a single original master, an intermediate template is fabricated featuring an inversed pyramid pattern using soft UV-NIL and subsequent wet chemical etch. By utilizing the slope of the inversed pyramid structures, the mask on the final substrate can be opened featuring tunable dimensions. Cryogenic etching based on SF6/O2 chemistry enables the creation of the final shrunk nanopatterns with smooth and vertical profile. The fabrication cycles involve only short imprinting and etch processes coping without costly electron beam writings. Therefore, the original microand nanostructure wafer can be shrunk into nanopatterns with tunable feature sizes at a constant pitch in a cost effective manner. The generated periodic nanopatterns can be adopted to the fields of NIL templates, photonic crystals, optics, energy conversion and
在本文中,设计了一个成本效益高的工艺链来缩小周期性纳米图案到可调的特征尺寸。最终图案的特征尺寸可以控制和调整。100毫米的全晶圆片具有130 nm、160 nm、190 nm和220 nm特征尺寸的方孔,由原始晶圆片制成,圆孔直径为350 nm。制造链涉及众所周知的技术,如蚀刻和软紫外纳米压印光刻(UV- nil)。基于单个原始母版,使用软UV-NIL和随后的湿化学蚀刻制作具有倒金字塔图案的中间模板。通过利用倒金字塔结构的斜率,最终基板上的掩膜可以打开,具有可调的尺寸。基于SF6/O2化学的低温蚀刻使最终缩小的纳米图案具有光滑和垂直的轮廓。制造周期只涉及短的压印和蚀刻过程,而不需要昂贵的电子束书写。因此,原始的微纳米结构晶片可以以经济有效的方式以恒定的间距缩小成具有可调特征尺寸的纳米图案。所生成的周期性纳米图案可应用于零模板、光子晶体、光学、能量转换和光学等领域
{"title":"A Fabrication Process for Nanopatterns Shrinkage with Variable Sizes for Large Area","authors":"S. Si, Lars Dittrich, M. Hoffmann","doi":"10.11159/ICNNFC17.129","DOIUrl":"https://doi.org/10.11159/ICNNFC17.129","url":null,"abstract":"In this paper, a cost efficient process chain is designed to shrink periodic nanopatterns to tunable feature sizes. The feature size of the final patterns can be controlled and adjusted. 100 mm full wafers featuring square holes with 130 nm, 160 nm, 190 nm and 220 nm feature sizes are fabricated from the original wafer containing circular holes with a diameter of 350 nm. The fabrication chain involves well-known technologies such as etching and soft UV nanoimprint lithography (UV-NIL). Based on a single original master, an intermediate template is fabricated featuring an inversed pyramid pattern using soft UV-NIL and subsequent wet chemical etch. By utilizing the slope of the inversed pyramid structures, the mask on the final substrate can be opened featuring tunable dimensions. Cryogenic etching based on SF6/O2 chemistry enables the creation of the final shrunk nanopatterns with smooth and vertical profile. The fabrication cycles involve only short imprinting and etch processes coping without costly electron beam writings. Therefore, the original microand nanostructure wafer can be shrunk into nanopatterns with tunable feature sizes at a constant pitch in a cost effective manner. The generated periodic nanopatterns can be adopted to the fields of NIL templates, photonic crystals, optics, energy conversion and","PeriodicalId":31009,"journal":{"name":"RAN","volume":"42 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82147324","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Interference of Silver Nanoparticles with Tumor Necrosis Factor Action in Epithelial Cells 银纳米粒子对上皮细胞肿瘤坏死因子作用的干扰
RAN
Pub Date : 2017-04-01 DOI: 10.11159/icnb17.116
Grądzka Iwona, Sikorska Katarzyna, Brzóska Kamil
Extended Abstract Silver nanoparticles (AgNPs), due to their antibacterial properties are widely used as additives to textiles, cosmetics, food packaging, surgical instruments or wound dressings. Being present in so many consumer goods, AgNPs are able to penetrate the human body via multiple paths [1]. The formation of reactive oxygen species (ROS) is believed to be the main mechanism of AgNPs action in a cell. ROS can launch both pro-survival and death signaling pathways depending on the level of oxidative stress induced [2]. Recently, we showed that AgNPs are able to activate NF-κB signaling pathway and expression of genes related to inflammatory and stress response [3]. Similar program is activated by tumor necrosis factor (TNF) – a major pro-inflammatory cytokine [4]. Our objective was to assess the possible interference of AgNPs (20 nm, BSA coated) with cellular response to TNF in two human cell lines: A549 lung adenocarcinoma and HepG2 liver hepatocellular carcinoma. Both types of cells absorbed AgNPs added to the medium as shown cytometrically by using side-scattered light. During 24-hour incubation, the effect of TNF and AgNPs on growth retardation and the incidence of cell death was additive and HepG2 cells were more sensitive to the agents studied. Analysis of the cell cycle discovered G1 arrest after TNF and S and G2/M arrest under AgNPs influence in both cell lines, whereas the combined treatment resulted in G1 and S accumulation in A549 and G2/M accumulation in HepG2 cells. Over a longer incubation period (7-12 days), in the clonogenicity test, the effect of TNF and AgNPs on the cell survival was synergistic. The effect of the selected signaling pathways inhibitors was tested using neutral red viability 24-hour assay. Surprisingly, the use of IKK II and IKK VII the inhi pathway – led to the increase of the cell viability in both cell lines treated with TNF, AgNPs or both agents simultaneously. Apart from end cellular effects, the expression of genes involved in the anti-oxidative defense and inflammatory response was analyzed by using real-time PCR. It was shown that the expression of heme oxygenase 1 (HMOX1), the protein induced by oxidative stress, was greatly enhanced in TNF and AgNPs treated cells compared to that observed after TNF alone. Similarly, AgNPs augmented the expression of pro-inflammatory cytokines CSF3 and IL-10. On the contrary, the expression of toll-like receptors TLR3 and TLR7, important for virus pathogen recognition, was significantly hampered by the addition of AgNPs. The presented results indicate that AgNPs change the final cellular result of TNF action and disrupt the cellular homeostasis, that can contribute to the development of malignancy or autoimmune diseases at the level of the organism. Therefore, an extended study is needed to provide more information about the nature and specificity of the functional interactions between TNF and AgNPs in cells. This work was supported by the grant 2014/13/D/NZ7/002
银纳米颗粒(AgNPs)由于其抗菌性能被广泛用作纺织品、化妆品、食品包装、手术器械或伤口敷料的添加剂。AgNPs存在于许多消费品中,能够通过多种途径渗透人体[1]。活性氧(ROS)的形成被认为是AgNPs在细胞中作用的主要机制。根据氧化应激诱导的水平,ROS可以启动促生存和促死亡信号通路[2]。最近,我们发现AgNPs能够激活NF-κB信号通路以及炎症和应激反应相关基因的表达[3]。类似的程序被肿瘤坏死因子(TNF)激活,TNF是一种主要的促炎细胞因子[4]。我们的目的是评估AgNPs (20 nm, BSA包被)可能干扰两种人类细胞系:A549肺腺癌和HepG2肝细胞癌对TNF的细胞反应。两种类型的细胞都吸收了添加到培养基中的AgNPs,通过侧散射光进行细胞测量。在24小时的孵育过程中,TNF和AgNPs对HepG2细胞生长迟缓和细胞死亡发生率的影响是叠加性的,并且HepG2细胞对所研究的药物更敏感。细胞周期分析发现,在AgNPs影响下,两种细胞系在TNF、S和G2/M阻滞后均出现G1阻滞,而联合处理导致A549细胞中G1和S积累,HepG2细胞中G2/M积累。在较长的潜伏期(7-12天)中,在克隆原性试验中,TNF和AgNPs对细胞存活的影响是协同的。采用中性红活力24小时法检测所选信号通路抑制剂的作用。令人惊讶的是,IKK II和IKK VII (inhi途径)的使用导致两种细胞系同时接受TNF、AgNPs或两种药物处理的细胞活力增加。除了末端细胞效应外,我们还利用实时荧光定量PCR分析了参与抗氧化防御和炎症反应的基因的表达。结果表明,氧化应激诱导的血红素加氧酶1 (HMOX1)的表达在TNF和AgNPs处理的细胞中比单独TNF处理的细胞显著增强。同样,AgNPs增强了促炎细胞因子CSF3和IL-10的表达。相反,对病毒病原体识别重要的toll样受体TLR3和TLR7的表达受到AgNPs的显著抑制。目前的结果表明,AgNPs改变TNF作用的最终细胞结果并破坏细胞稳态,这可能在机体水平上促进恶性肿瘤或自身免疫性疾病的发展。因此,需要进一步的研究来提供更多关于细胞中TNF和AgNPs之间功能相互作用的性质和特异性的信息。本研究得到波兰国家科学中心2014/13/D/NZ7/00286项目资助。
{"title":"Interference of Silver Nanoparticles with Tumor Necrosis Factor Action in Epithelial Cells","authors":"Grądzka Iwona, Sikorska Katarzyna, Brzóska Kamil","doi":"10.11159/icnb17.116","DOIUrl":"https://doi.org/10.11159/icnb17.116","url":null,"abstract":"Extended Abstract Silver nanoparticles (AgNPs), due to their antibacterial properties are widely used as additives to textiles, cosmetics, food packaging, surgical instruments or wound dressings. Being present in so many consumer goods, AgNPs are able to penetrate the human body via multiple paths [1]. The formation of reactive oxygen species (ROS) is believed to be the main mechanism of AgNPs action in a cell. ROS can launch both pro-survival and death signaling pathways depending on the level of oxidative stress induced [2]. Recently, we showed that AgNPs are able to activate NF-κB signaling pathway and expression of genes related to inflammatory and stress response [3]. Similar program is activated by tumor necrosis factor (TNF) – a major pro-inflammatory cytokine [4]. Our objective was to assess the possible interference of AgNPs (20 nm, BSA coated) with cellular response to TNF in two human cell lines: A549 lung adenocarcinoma and HepG2 liver hepatocellular carcinoma. Both types of cells absorbed AgNPs added to the medium as shown cytometrically by using side-scattered light. During 24-hour incubation, the effect of TNF and AgNPs on growth retardation and the incidence of cell death was additive and HepG2 cells were more sensitive to the agents studied. Analysis of the cell cycle discovered G1 arrest after TNF and S and G2/M arrest under AgNPs influence in both cell lines, whereas the combined treatment resulted in G1 and S accumulation in A549 and G2/M accumulation in HepG2 cells. Over a longer incubation period (7-12 days), in the clonogenicity test, the effect of TNF and AgNPs on the cell survival was synergistic. The effect of the selected signaling pathways inhibitors was tested using neutral red viability 24-hour assay. Surprisingly, the use of IKK II and IKK VII the inhi pathway – led to the increase of the cell viability in both cell lines treated with TNF, AgNPs or both agents simultaneously. Apart from end cellular effects, the expression of genes involved in the anti-oxidative defense and inflammatory response was analyzed by using real-time PCR. It was shown that the expression of heme oxygenase 1 (HMOX1), the protein induced by oxidative stress, was greatly enhanced in TNF and AgNPs treated cells compared to that observed after TNF alone. Similarly, AgNPs augmented the expression of pro-inflammatory cytokines CSF3 and IL-10. On the contrary, the expression of toll-like receptors TLR3 and TLR7, important for virus pathogen recognition, was significantly hampered by the addition of AgNPs. The presented results indicate that AgNPs change the final cellular result of TNF action and disrupt the cellular homeostasis, that can contribute to the development of malignancy or autoimmune diseases at the level of the organism. Therefore, an extended study is needed to provide more information about the nature and specificity of the functional interactions between TNF and AgNPs in cells. This work was supported by the grant 2014/13/D/NZ7/002","PeriodicalId":31009,"journal":{"name":"RAN","volume":"167 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80516638","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mechanical Cell Disruption Using Hierarchical Micro-Nano Structures on Nanoporous Alumina Filter 纳米多孔氧化铝过滤器上分层微纳结构的机械细胞破坏
RAN
Pub Date : 2017-04-01 DOI: 10.11159/ICNNFC17.111
Yong Hun Lee, E. Han, Y. Park, B. Kim, Y. Seo
Extended Abstract Cell disruption is essential process in molecular biology and biomedical engineering for investigation of DNA, RNA, virus and protein in cell. Generally, there are some methods for cell disruption or cell lysis such as chemical, electrical and mechanical method. [1, 2] Chemical cell lysis is method that dissolve cell envelope and nucleus using cell lysis buffer and lysate from this process contains lysis buffer which couldn’t know the composition. Electrical and mechanical cell disruption methods required external equipment and shows low cell disruption efficiency. Especially, mechanical cell disruption is easy and quick method and studied using microstructures for increment of cell disruption efficiency. [3, 4] However, most of microstructures such as microchannel or microblade has critical dimension around 3μm and cell could through-out by deformation of its body. [5, 6] In this study, we presents the mechanical cell disruption using hierarchical micro-nano structures on nanoporous alumina filter. Hierarchical micro-nano structures on nanoporous alumina filter was fabricated aluminium wet etching process and multi-step anodic aluminium oxidation process. Pure aluminium sheet (5N, 1mm thickness) was mechanical and electro-polished for mirror-like surface. Next, aluminium sheet was dipped in aluminium etchant of CuCl2 base for fabrication of micro-structures. During aluminium etching process, micro-structures were formed by chipping off a grain boundary of aluminium. Multi-step anodic aluminium oxidation process was carried out for fabrication of nano-structures and filter body. Aluminium that formed micro-structures on surface was anodized twice in 0.3M phosphoric acid aqueous solution of -5°C under 180V. Formed nanoporous alumina structure was expanded by wet etching process for forming of spike-like nanostructure shape in 0.1M phosphoric acid aqueous solution of 35°C. 3 rd anodic aluminium oxidation process was carried out for fabrication of filter body under same condition mentioned above for 40hours. Finally, aluminium was removed and barrier layer of nanoporous alumina was opened by wet etching process. For mechanical cell disruption, NIH3T3 fibroblast cells (1 ×10 6 cells/ml) in PBS (phosphate buffered saline) were injected through hierarchical micro-nano structures on nanoporous alumina filter which assembled with commercial filter holder by air pressure (5bar). Cell disruption efficiency was evaluated by quantification of DNA and protein in lysate. Concentration of DNA and protein were quantified using DNA isolation kit (DNeasy, Quiagen) and Bradford assay, respectively. According to results, 5.1 ± 1.3 μg/ml of DNA and 46 ± 11 μg/ml of protein were detected from lysate. In cell disruption process using hierarchical micro-nano structure on nanoporous alumina filter, cell envelope and nucleus were teared by micro-structures and un-teared nucleus by micro-structure was disrupted by nano-structures. This results shows cell
细胞破坏是分子生物学和生物医学工程中研究细胞内DNA、RNA、病毒和蛋白质的重要过程。一般来说,细胞破坏或细胞裂解的方法有化学法、电法和机械法。[1,2]化学细胞裂解是用细胞裂解缓冲液溶解细胞包膜和细胞核的方法,裂解液中含有不知道其成分的裂解缓冲液。电气和机械的细胞破坏方法需要外部设备,并且细胞破坏效率低。特别是机械破坏细胞是一种简单快捷的方法,利用微结构提高细胞破坏效率。[3,4]然而,微通道或微叶片等微结构的临界尺寸大多在3μm左右,细胞可以通过其本体变形而穿出。[5,6]在这项研究中,我们提出了在纳米多孔氧化铝过滤器上使用分层微纳结构的机械细胞破坏。采用湿法蚀刻工艺和多步阳极铝氧化工艺在纳米多孔氧化铝过滤器上制备了分层微纳结构。纯铝板(5N, 1mm厚度)经机械和电抛光,表面呈镜面状。然后,将铝板浸入CuCl2基铝蚀刻剂中制备微结构。在铝蚀刻过程中,通过切掉铝的晶界形成微观结构。采用多步阳极铝氧化法制备了纳米结构和过滤体。在-5℃的0.3M磷酸水溶液中,180V下阳极氧化两次,铝表面形成微观结构。在35℃的0.1M磷酸水溶液中,采用湿法刻蚀法对形成的纳米孔氧化铝结构进行膨胀,形成尖刺状纳米结构形状。在相同条件下,进行第三次阳极铝氧化工艺制作过滤体,工艺时间为40h。最后,采用湿法刻蚀法去除铝,打开纳米多孔氧化铝阻挡层。为了对细胞进行机械破坏,将NIH3T3成纤维细胞(1 ×10 6个细胞/ml)在PBS(磷酸盐缓冲盐水)中通过分层微纳结构注射到纳米孔氧化铝过滤器上,该过滤器在空气压力(5bar)下与商用过滤器支架组装。通过定量分析裂解液中的DNA和蛋白质来评估细胞破坏效率。分别用DNA分离试剂盒(DNeasy, Quiagen)和Bradford法测定DNA和蛋白质的浓度。结果显示,裂解液中DNA含量为5.1±1.3 μg/ml,蛋白质含量为46±11 μg/ml。在纳米多孔氧化铝过滤器上采用分层微纳结构破坏细胞的过程中,微结构撕裂细胞包膜和细胞核,微结构破坏未撕裂的细胞核。结果表明,与理论值相比,细胞包膜破坏率为32%,细胞核破坏率为92%。[7,8]本研究得到教育部基础科学研究计划项目(NRF- 2014r1a1a2057692)和先锋研究中心项目(NRF-20120009575)的资助。
{"title":"Mechanical Cell Disruption Using Hierarchical Micro-Nano Structures on Nanoporous Alumina Filter","authors":"Yong Hun Lee, E. Han, Y. Park, B. Kim, Y. Seo","doi":"10.11159/ICNNFC17.111","DOIUrl":"https://doi.org/10.11159/ICNNFC17.111","url":null,"abstract":"Extended Abstract Cell disruption is essential process in molecular biology and biomedical engineering for investigation of DNA, RNA, virus and protein in cell. Generally, there are some methods for cell disruption or cell lysis such as chemical, electrical and mechanical method. [1, 2] Chemical cell lysis is method that dissolve cell envelope and nucleus using cell lysis buffer and lysate from this process contains lysis buffer which couldn’t know the composition. Electrical and mechanical cell disruption methods required external equipment and shows low cell disruption efficiency. Especially, mechanical cell disruption is easy and quick method and studied using microstructures for increment of cell disruption efficiency. [3, 4] However, most of microstructures such as microchannel or microblade has critical dimension around 3μm and cell could through-out by deformation of its body. [5, 6] In this study, we presents the mechanical cell disruption using hierarchical micro-nano structures on nanoporous alumina filter. Hierarchical micro-nano structures on nanoporous alumina filter was fabricated aluminium wet etching process and multi-step anodic aluminium oxidation process. Pure aluminium sheet (5N, 1mm thickness) was mechanical and electro-polished for mirror-like surface. Next, aluminium sheet was dipped in aluminium etchant of CuCl2 base for fabrication of micro-structures. During aluminium etching process, micro-structures were formed by chipping off a grain boundary of aluminium. Multi-step anodic aluminium oxidation process was carried out for fabrication of nano-structures and filter body. Aluminium that formed micro-structures on surface was anodized twice in 0.3M phosphoric acid aqueous solution of -5°C under 180V. Formed nanoporous alumina structure was expanded by wet etching process for forming of spike-like nanostructure shape in 0.1M phosphoric acid aqueous solution of 35°C. 3 rd anodic aluminium oxidation process was carried out for fabrication of filter body under same condition mentioned above for 40hours. Finally, aluminium was removed and barrier layer of nanoporous alumina was opened by wet etching process. For mechanical cell disruption, NIH3T3 fibroblast cells (1 ×10 6 cells/ml) in PBS (phosphate buffered saline) were injected through hierarchical micro-nano structures on nanoporous alumina filter which assembled with commercial filter holder by air pressure (5bar). Cell disruption efficiency was evaluated by quantification of DNA and protein in lysate. Concentration of DNA and protein were quantified using DNA isolation kit (DNeasy, Quiagen) and Bradford assay, respectively. According to results, 5.1 ± 1.3 μg/ml of DNA and 46 ± 11 μg/ml of protein were detected from lysate. In cell disruption process using hierarchical micro-nano structure on nanoporous alumina filter, cell envelope and nucleus were teared by micro-structures and un-teared nucleus by micro-structure was disrupted by nano-structures. This results shows cell ","PeriodicalId":31009,"journal":{"name":"RAN","volume":"17 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80585860","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cu(II)-Imprinted Nanoparticles for Real Time Detection of Cu(II) Ions Cu(II)-印迹纳米粒子用于Cu(II)离子的实时检测
RAN
Pub Date : 2017-04-01 DOI: 10.11159/ICNEI17.106
M. Andaç, Nihan Aydoğan, Monireh Bakhshpour, A. Denizli
{"title":"Cu(II)-Imprinted Nanoparticles for Real Time Detection of Cu(II) Ions","authors":"M. Andaç, Nihan Aydoğan, Monireh Bakhshpour, A. Denizli","doi":"10.11159/ICNEI17.106","DOIUrl":"https://doi.org/10.11159/ICNEI17.106","url":null,"abstract":"","PeriodicalId":31009,"journal":{"name":"RAN","volume":"26 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73374612","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Theoretical-Experimental Comparison of CdSe Quantum Dot Optical Properties CdSe量子点光学特性的理论与实验比较
RAN
Pub Date : 2017-04-01 DOI: 10.11159/ICNMS17.105
I. Oliva, Sandra Alvarenga, C. Rudamas
In this work, we have studied the optical properties of CdSe quantum dots (QDs) with different sizes. Using the SIESTA code and the Kramers-Kronig relations, we have computed the imaginary part of the dielectric constant and the density of states (DOS). The absorption spectra are compared to experimental results from samples fabricated using the thermal decomposition method and a good agreement was obtained. The experimental band edge absorption could be associated to a specific optical transition in our QDs. A well defined second absorption band has been observed in our theoretical results. The energy maximum of these bands follow the expected quantum size effect. However, we do not observed the increase of the energy difference between them, reported by other authors. The reducing of absorption band intensity when the quantum dot size increases, has been seen. Preliminary density of states calculations, also reported in this work, allowed the association of Cdor Se-character to the energy states in our samples.
在这项工作中,我们研究了不同尺寸的CdSe量子点的光学性质。利用SIESTA代码和Kramers-Kronig关系,我们计算了介电常数的虚部和态密度(DOS)。将吸收光谱与热分解法制备样品的实验结果进行了比较,结果吻合较好。实验带边吸收可能与量子点中的特定光学跃迁有关。在我们的理论结果中观察到一个明确的第二吸收带。这些能带的能量最大值遵循预期的量子尺寸效应。然而,我们没有观察到它们之间能量差的增加,其他作者报道过。随着量子点尺寸的增大,吸收带强度减小。初步的态密度计算,也在这项工作中报道,允许我们的样品中的Cdor - se特征与能态的关联。
{"title":"A Theoretical-Experimental Comparison of CdSe Quantum Dot Optical Properties","authors":"I. Oliva, Sandra Alvarenga, C. Rudamas","doi":"10.11159/ICNMS17.105","DOIUrl":"https://doi.org/10.11159/ICNMS17.105","url":null,"abstract":"In this work, we have studied the optical properties of CdSe quantum dots (QDs) with different sizes. Using the SIESTA code and the Kramers-Kronig relations, we have computed the imaginary part of the dielectric constant and the density of states (DOS). The absorption spectra are compared to experimental results from samples fabricated using the thermal decomposition method and a good agreement was obtained. The experimental band edge absorption could be associated to a specific optical transition in our QDs. A well defined second absorption band has been observed in our theoretical results. The energy maximum of these bands follow the expected quantum size effect. However, we do not observed the increase of the energy difference between them, reported by other authors. The reducing of absorption band intensity when the quantum dot size increases, has been seen. Preliminary density of states calculations, also reported in this work, allowed the association of Cdor Se-character to the energy states in our samples.","PeriodicalId":31009,"journal":{"name":"RAN","volume":"120 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72537383","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Growth of ZnO Nanorod Film on Glass Substrate by Nitric Acid Assisted Aqueous Solution Deposition 硝酸辅助水溶液沉积法在玻璃基板上生长ZnO纳米棒薄膜
RAN
Pub Date : 2017-04-01 DOI: 10.11159/ICNNFC17.121
Ming-kwei Lee, Mu Wang, Hao Wang, Chang-Chin Tsai, Cheng-Yu Kung, Chiamin Yang, Huan-Chi Lung
In this paper, the growth of ZnO nanorod film transformed from ZnO nanorod array on glass substrate was investigated. ZnO seed layer was first prepared on substrate by RF sputtering. Zinc nitrate and hexamethylenetetramine were used as precursors for the growth of ZnO nanorod array on glass substrate at 50 o C. The aqueous solution was assisted with the incorporation of nitric acid to increase the growth rate and the grain size of ZnO nanorod. With the growth time, ZnO nanorod film is gradually transformed from ZnO nanorod array.
本文研究了由ZnO纳米棒阵列在玻璃衬底上转化成ZnO纳米棒薄膜的生长。采用射频溅射法制备了ZnO种子层。以硝酸锌和六亚甲基四胺为前驱体,在50℃条件下在玻璃基板上生长ZnO纳米棒阵列,并在硝酸的辅助下提高ZnO纳米棒的生长速度和晶粒尺寸。随着生长时间的延长,ZnO纳米棒阵列逐渐转变为ZnO纳米棒薄膜。
{"title":"Growth of ZnO Nanorod Film on Glass Substrate by Nitric Acid Assisted Aqueous Solution Deposition","authors":"Ming-kwei Lee, Mu Wang, Hao Wang, Chang-Chin Tsai, Cheng-Yu Kung, Chiamin Yang, Huan-Chi Lung","doi":"10.11159/ICNNFC17.121","DOIUrl":"https://doi.org/10.11159/ICNNFC17.121","url":null,"abstract":"In this paper, the growth of ZnO nanorod film transformed from ZnO nanorod array on glass substrate was investigated. ZnO seed layer was first prepared on substrate by RF sputtering. Zinc nitrate and hexamethylenetetramine were used as precursors for the growth of ZnO nanorod array on glass substrate at 50 o C. The aqueous solution was assisted with the incorporation of nitric acid to increase the growth rate and the grain size of ZnO nanorod. With the growth time, ZnO nanorod film is gradually transformed from ZnO nanorod array.","PeriodicalId":31009,"journal":{"name":"RAN","volume":"38 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90192658","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Polyamide Nanofiber Composites for Organic Pollutant Removal and Chemical Warfare Protection 聚酰胺纳米纤维复合材料的有机污染物去除和化学战防护
RAN
Pub Date : 2017-04-01 DOI: 10.11159/ICNEI17.109
Junho Chung, Daeyeon Won, Junhyung Lee, Changkyun Kim, S. Kwak
Extended Abstract Polymer nanofiber composites for the treatment of hazardous compounds are of considerable scientific and technological interest. In this study, polyamide nanofiber for organic pollutant removal and chemical warfare protection is discussed. The effect of position of functional materials in nanofiber matrix on the photocatalytic activity was studied by comparing the Ag-TiO2-decorated nylon nanofiber composite (AT-sur-NF) and Ag-TiO2-embedded nylon nanofiber composite (AT-in-NF) [1]. We find that AT-sur-NF shows better photocatalytic activity compared to the photocatalytic activity of AT-in-NF. Based on these results, nylon and meta-aramid nanofibers decorated by various functional nanomaterials were fabricated. The electrospun meta-aramid nanofiber composites exhibit poor chemical stability because of the salt molecules remaining between meta-aramid chains [2]. The chemical stability of meta-aramid nanofiber composites were improved by removing salt molecules during washing and additional thermal treatment. The polyamide nanofiber composites were stacked to enhance mechanical properties and resistivity to chemical warfare agents (CWAs). By controlling the stacking of polyamide nanofiber composites, thickness, weight density, and cool/warm feeling are optimized. In addition, the assemblies exhibit enough resistivity to CWAs while still maintain water vapor transmission to allow evaporation of sweat on the skin. Further study on the thermal properties and microstructure of nylon nanofibers reveals that the chains rigidity and thermal stability increase with decreasing diameter of nylon nanofibers.
高分子纳米纤维复合材料处理有害化合物具有重要的科学和技术意义。本文探讨了聚酰胺纳米纤维在有机污染物去除和化学战防护方面的应用。通过对比ag - tio2装饰尼龙纳米纤维复合材料(AT-sur-NF)和ag - tio2包埋尼龙纳米纤维复合材料(AT-in-NF)[1],研究了功能材料在纳米纤维基体中的位置对光催化活性的影响。我们发现AT-sur-NF比AT-in-NF具有更好的光催化活性。在此基础上,制备了不同功能纳米材料修饰的尼龙和间芳纶纳米纤维。静电纺间芳纶纳米纤维复合材料的化学稳定性较差,主要是由于盐分子残留在间芳纶链[2]之间。通过去除洗涤过程中的盐分子和额外的热处理,提高了间芳纶纳米纤维复合材料的化学稳定性。通过对聚酰胺纳米纤维复合材料的叠层处理,提高了复合材料的力学性能和抗化学战剂的电阻率。通过控制聚酰胺纳米纤维复合材料的堆叠,优化了材料的厚度、重量密度和冷暖感觉。此外,该组件对cwa具有足够的电阻率,同时仍然保持水蒸气传输,使皮肤上的汗水蒸发。对尼龙纳米纤维的热性能和微观结构的进一步研究表明,随着尼龙纳米纤维直径的减小,链的刚度和热稳定性增加。
{"title":"Polyamide Nanofiber Composites for Organic Pollutant Removal and Chemical Warfare Protection","authors":"Junho Chung, Daeyeon Won, Junhyung Lee, Changkyun Kim, S. Kwak","doi":"10.11159/ICNEI17.109","DOIUrl":"https://doi.org/10.11159/ICNEI17.109","url":null,"abstract":"Extended Abstract Polymer nanofiber composites for the treatment of hazardous compounds are of considerable scientific and technological interest. In this study, polyamide nanofiber for organic pollutant removal and chemical warfare protection is discussed. The effect of position of functional materials in nanofiber matrix on the photocatalytic activity was studied by comparing the Ag-TiO2-decorated nylon nanofiber composite (AT-sur-NF) and Ag-TiO2-embedded nylon nanofiber composite (AT-in-NF) [1]. We find that AT-sur-NF shows better photocatalytic activity compared to the photocatalytic activity of AT-in-NF. Based on these results, nylon and meta-aramid nanofibers decorated by various functional nanomaterials were fabricated. The electrospun meta-aramid nanofiber composites exhibit poor chemical stability because of the salt molecules remaining between meta-aramid chains [2]. The chemical stability of meta-aramid nanofiber composites were improved by removing salt molecules during washing and additional thermal treatment. The polyamide nanofiber composites were stacked to enhance mechanical properties and resistivity to chemical warfare agents (CWAs). By controlling the stacking of polyamide nanofiber composites, thickness, weight density, and cool/warm feeling are optimized. In addition, the assemblies exhibit enough resistivity to CWAs while still maintain water vapor transmission to allow evaporation of sweat on the skin. Further study on the thermal properties and microstructure of nylon nanofibers reveals that the chains rigidity and thermal stability increase with decreasing diameter of nylon nanofibers.","PeriodicalId":31009,"journal":{"name":"RAN","volume":"89 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89921339","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
RAN
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:481959085
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