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Effect of concentration and ionic strength on the lower critical solution temperature of poly(N-isopropylacrylamide) investigated by small-angle X-ray scattering 小角度X射线散射研究浓度和离子强度对聚N-异丙基丙烯酰胺溶液下临界温度的影响
IF 1.2 4区 材料科学 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2021-09-16 DOI: 10.1080/1539445X.2021.1979041
Bence Fehér, I. Varga, J. S. Pedersen
ABSTRACT Thermoresponsive polymers, with special emphasis on poly(N-isopropylacrylamide) (PNIPAAM) have been the focus of several investigations due to its potential applications in many fields of physical and polymer chemistry. PNIPAAM has a “lower critical solution temperature” at 32°C. The LCST can be finely tuned by copolymerization with hydrophobic or hydrophilic comonomers, and with a change of physical chemical parameters, such as ionic strength of the solution. We investigated the effect of polymer concentration on the LCST in two different solution environment, in pure water and in 50 mM NaCl solution with small-angle X-ray scattering (SAXS) of relatively low molecular mass polymers. We showed that the radius of gyration of the pNIPAAM chains increases with the addition of NaCl to the system due to the low level of specific adsorption of chloride ions on the polymer, whilst increasing the temperature causes a shrinkage of the polymer chains. Furthermore, by increasing the temperature the attractive interaction between the individual polymer chains is enhanced which turns into aggregation at the LCST.
摘要热响应聚合物,特别是聚N-异丙基丙烯酰胺(PNIPAAM),由于其在物理和聚合物化学的许多领域中的潜在应用,一直是研究的焦点。PNIPAAM的“较低临界溶液温度”为32°C。LCST可以通过与疏水性或亲水性共聚单体共聚,并通过改变物理化学参数(如溶液的离子强度)进行微调。我们用相对低分子质量聚合物的小角度X射线散射(SAXS)研究了在纯水和50mM NaCl溶液中两种不同溶液环境中聚合物浓度对LCST的影响。我们发现,由于氯离子在聚合物上的比吸附水平较低,pNIPAAM链的回转半径随着向体系中加入NaCl而增加,同时温度的升高会导致聚合物链的收缩。此外,通过提高温度,单个聚合物链之间的吸引力相互作用增强,在LCST处转变为聚集。
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引用次数: 1
Self-assembly of multiple stimulus response copolymer by ATRP in different media 多刺激响应共聚物在不同介质中的自组装
IF 1.2 4区 材料科学 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2021-09-01 DOI: 10.1080/1539445X.2021.1945627
Xilai Zhou, Yazhen Wang, Han Xin, Shaobo Dong, Tianyu Lan, Liwu Zu, Chenglong Wang, Li Liu
ABSTRACT The novel pH and thermo-sensitive amphiphilic triblock copolymer poly(methyl methacrylate)-block-poly(N-isopropylacrylamide)-block-poly[N,N-(dimethylamino) ethyl methacrylate] (PMMA-b-PNIPAM-b-PDMAEMA) was synthesized by ATRP. We have prepared the AB amphiphilic copolymer (PMMA-b-PNIPAM) and ABC amphiphilic triblock copolymer (PMMA-b-PNIPAM-b-PDMAEMA) of expected molecular mass. It was characterized by GPC,1HNMR and FT-IR spectroscopy. The AB amphiphilic copolymer ability of temperature response and the morphology of self-assembly micelles different in toluene, THF, and DMF. ABC amphiphilic triblock copolymer self-assembled petal structure in alkaline aqueous solution, and lamellar structure in acidic aqueous solution. Moreover, the transmittance of micellar solution changes with the increase of temperature; these changes reflect the pH and thermo-sensitivity of the block copolymer. The micelles behavior and morphology of the system were studied by transmission electron microscopy (TEM) and dynamic light scattering (DLS).
摘要采用ATRP法合成了新型pH和热敏两亲性三嵌段共聚物聚(甲基丙烯酸甲酯)-嵌段聚(N-异丙基丙烯酰胺)-嵌段聚[N,N-(二甲氨基)甲基丙烯酸乙酯](PMMA-b-PNIPAM-b-PDMAEMA)。我们制备了预期分子质量的AB两亲共聚物(PMMA-b-PNIPAM)和ABC两亲三嵌段共聚物(PMMA-b-PNIPAM-b- pdmaema)。用GPC、1HNMR和FT-IR对其进行了表征。AB两亲共聚物在甲苯、四氢呋喃和DMF中的温度响应能力和自组装胶束形态不同。ABC两亲性三嵌段共聚物在碱性水溶液中自组装花瓣结构,在酸性水溶液中自组装片层结构。胶束溶液的透过率随温度的升高而变化;这些变化反映了嵌段共聚物的pH值和热敏性。利用透射电子显微镜(TEM)和动态光散射(DLS)研究了体系的胶束行为和形貌。
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引用次数: 2
Facile synthesis and high volumetric capacitance of holey graphene film for supercapacitor electrodes with optimizing preparation conditions 优化制备条件,实现超级电容器电极用多孔石墨烯薄膜的简易合成和高体积电容
IF 1.2 4区 材料科学 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2021-08-13 DOI: 10.1080/1539445X.2021.1928703
Benshuo Zhu, Hua Li, Yujie Chen, Hezhou Liu
ABSTRACT For miniaturized portable energy storage devices with limited space, electrode materials are needed to be developed in the direction of reducing the occupied volume without compromising high specific capacitance and stable cycling ability. Herein, a facile strategy was developed to fabricate a free-standing binder-free holey graphene film as a supercapacitor electrode. In this material mechanism, holey structure in graphene sheets provides abundant ion transport channels and accelerates ion diffusion efficiency, which could guarantee that this film performs a high packing density without compromising electrochemical performance. After being properly optimized on the amount of H2O2 added and the mechanical pressure while preparing, this electrode film could consequently perform a high volumetric capacitance of 406 F cm−3 and excellent cycle stability with a packing density of 1.34 g cm−3. Therefore, this kind of densely packed electrode film with excellent electrochemical performance is of great significance for the development of miniaturized portable energy storage devices.
摘要:对于空间有限的小型便携式储能设备,需要在不影响高比电容和稳定循环能力的情况下,朝着减少占用体积的方向发展电极材料。在此,开发了一种简单的策略来制备作为超级电容器电极的无粘合剂的独立多孔石墨烯膜。在这种材料机制中,石墨烯片中的多孔结构提供了丰富的离子传输通道,并加速了离子扩散效率,这可以保证该膜在不影响电化学性能的情况下具有高堆积密度。在对H2O2的添加量和制备时的机械压力进行适当优化后,该电极膜可以实现406 F cm−3的高体积电容和1.34 g cm−3填充密度的优异循环稳定性。因此,这种具有优异电化学性能的致密电极膜对开发小型化便携式储能装置具有重要意义。
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引用次数: 2
Biomolecules of Similar Charge Polarity Form Hybrid Gel 具有相似电荷极性的生物分子形成杂化凝胶
IF 1.2 4区 材料科学 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2021-08-13 DOI: 10.1080/1539445X.2021.1964527
P. Pandey, V. Aswal, J. Kohlbrecher, H. Bohidar
ABSTRACT We report intermolecular gelation of deoxyribonucleic acid (DNA) and folic acid (FA, 1% (w/v) and DNA, 0.1–0.5% (w/v)) in Dimethyl Sulfoxide (DMSO)-water solution despite both having similar net charge. Zeta potential ζ of the biopolymers was, ζDNA = −58 and ζFA = −18 mV, therefore, formation of a self-organized hybrid network structure to assign sufficient rigidity to the gel must happen in the environment of electrostatic repulsion persisting between the inter and intra polymer segments. Regardless, a stable supramolecular hydrogel was formed at room temperature of 25° C with the DNA–FA complex displaying a zeta potential of ζcomplex = −21 mV. The gel strength (low frequency storage modulus, G 0) was tunable from ≈ 500 to 50 Pa, and gelation temperature T gel from 70 to 60° C, decreasing with DNA content. These soft gels were systematically characterized over several decades of time (dynamic light scattering), and length scales (small angle neutron scattering), rheology and scanning electron microscopy to obtain a deeper understanding of the self-assembly of the DNA in the FA-dominant solution. These gels formed of same polarity biopolymers, and in a milieu of strong electrostatic repulsion, make these belong to a special class of soft matter not well studied in the past.
我们报道了脱氧核糖核酸(DNA)和叶酸(FA, 1% (w/v)和DNA, 0.1-0.5% (w/v))在二甲基亚砜(DMSO)水溶液中的分子间凝胶化,尽管两者具有相似的净电荷。生物聚合物的ζ电位ζ为,ζ dna =−58,ζ fa =−18 mV,因此,自组织杂化网络结构的形成必须发生在聚合物段间和段内持续存在静电排斥的环境中,以赋予凝胶足够的刚性。无论如何,在室温25℃下形成了稳定的超分子水凝胶,DNA-FA络合物的ζ电位为ζ络合物=−21 mV。凝胶强度(低频存储模量g0)可调范围为≈500 ~ 50 Pa,凝胶温度T可调范围为70 ~ 60℃,凝胶强度随DNA含量的增加而降低。这些软凝胶在几十年的时间(动态光散射)、长度尺度(小角中子散射)、流变学和扫描电镜下进行了系统的表征,以更深入地了解DNA在fa优势溶液中的自组装。这些凝胶是由相同极性的生物聚合物形成的,并且在强静电排斥的环境中,使它们属于一类特殊的软物质,过去没有得到很好的研究。
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引用次数: 0
The ensemble of immobilized superparamagnetic nanoparticles: the role of the spatial distribution in the sample 固定化超顺磁性纳米粒子系综:在样品中空间分布的作用
IF 1.2 4区 材料科学 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2021-08-08 DOI: 10.1080/1539445X.2021.1957933
A. Solovyova, S. Sokolsky, E. Elfimova
ABSTRACT In this work, static, thermodynamic and magnetic properties of interacting superparamagnetic nanoparticles have been studied using theory and computer simulation. Two types of particles’ distributions in the sample have been considered: (a) at the nodes of the simple cubic lattice and (b) by the random way. It was assumed that the directions of the easy axes for all particles were parallel to each other and directed at an angle to the external magnetic field. The theoretical approach is based on the expanding of the Helmholtz free energy into the classical virial series up to the second virial coefficient. The analytical expressions of the Helmholtz free energy for both textures allow us to obtain theoretical predictions for the static magnetization and the isochoric heat capacity. These characteristics turned out in a good agreement with the Monte-Carlo simulation data in the broad range of considered system parameters. In a zero and moderate external magnetic fields, the new theory allows to describe the numerical calculations much more efficient than the ideal approximations, for which the interparticle dipole-dipole interactions were neglected.
本文运用理论和计算机模拟的方法,研究了相互作用的超顺磁性纳米颗粒的静态、热力学和磁学性质。考虑了两种类型的粒子在样品中的分布:(a)在简单立方晶格的节点处和(b)通过随机方式。假设所有粒子的易轴方向彼此平行,并与外部磁场成一定角度。理论方法是基于将亥姆霍兹自由能扩展到经典维里级数,直到第二维里系数。两种纹理的亥姆霍兹自由能的解析表达式使我们能够获得静态磁化和等容热容的理论预测。在所考虑的系统参数的大范围内,这些特性与蒙特卡罗模拟数据非常一致。在零和中等外部磁场中,新理论可以比理想近似更有效地描述数值计算,而理想近似忽略了粒子间偶极-偶极相互作用。
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引用次数: 1
Hydroxyapatite incorporated bacterial cellulose hydrogels as a cost-effective 3D cell culture platform 羟基磷灰石结合细菌纤维素水凝胶作为一个具有成本效益的3D细胞培养平台
IF 1.2 4区 材料科学 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2021-07-05 DOI: 10.1080/1539445X.2021.1944208
S. S. Athukorala, Chathudina J. Liyanage, A. Jayasundera
ABSTRACT For cell and tissue physiology research, drug discovery, and growing replacement tissues for regenerative medicine, accurate and cost-efficient in vitro techniques are increasingly demanded. The conventional model for in vitro cell culture is the two-dimensional (2D) culture. Yet, cells have been found to be more native when they are grown in 3D conditions. We present here the development and evaluation of biological properties of bacterial cellulose/hydroxyapatite (BC/HA) nanocomposite hydrogel as a potential 3D cell-culture platform. The synthesized composites were characterized using Scanning Electron Microscopy (SEM), Atomic Force Microscopy (AFM), Swelling measurements and Celltiter 96® Aqueous One Solution Cell Proliferation Assay (MTS) using mouse fibroblast cell line (L – 929). The arrangement of composites shown in SEM and AFM images closely resembles the native extracellular matrices (ECM) showing the potential to act as a viable substrate for cell culture. The composites exhibited high swelling ratio (5.31–5.81), indicating enhanced moisture absorption and potential for nutrient exchange. The in vitro biocompatibility results indicated significantly high percentage cell proliferation (85.20%-88.30%). These findings indicate that the BC/HA composites are potential candidates for 3D cell-culture applications.
对于细胞和组织生理学研究、药物发现和再生医学中生长的替代组织,越来越需要精确和经济高效的体外技术。体外细胞培养的传统模型是二维(2D)培养。然而,已经发现细胞在3D条件下生长时更加原生。我们在此介绍了细菌纤维素/羟基磷灰石(BC/HA)纳米复合水凝胶作为潜在的三维细胞培养平台的生物学特性的开发和评估。采用扫描电镜(SEM)、原子力显微镜(AFM)、肿胀测量和Celltiter 96®水溶液细胞增殖试验(MTS)对合成的复合材料进行了表征,实验采用小鼠成纤维细胞系(L - 929)。SEM和AFM图像显示的复合材料的排列与天然细胞外基质(ECM)非常相似,显示出作为细胞培养可行底物的潜力。复合材料具有较高的溶胀率(5.31-5.81),表明复合材料具有较强的吸湿性和养分交换潜力。体外生物相容性结果显示细胞增殖率显著提高(85.20% ~ 88.30%)。这些发现表明,BC/HA复合材料是3D细胞培养应用的潜在候选者。
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引用次数: 3
Structure and dynamics in active matter systems 活性物质系统的结构与动力学
IF 1.2 4区 材料科学 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2021-07-03 DOI: 10.1080/1539445X.2021.1938609
S. Das
Active matter systems are made of self-propelling particles and make ideal ground for studies of out-ofequilibrium phenomena. The self-propulsion is fueled by continuous drawing of energy from the environment at the single-particle scale. Examples of such systems are common, covering a wide range of lengths, from molecular level biological systems to large societies of animals. It is, however, not necessary that the constituents should only be living objects. These systems often exhibit fascinating patterns and dynamics. Understanding such collective phenomena is of importance from fundamental as well as practical points of view. Despite conceptual difficulties, [4–7] e.g., with respect to the definition of temperature, significant advancement has been made at the theoretical level. In the domain of nonequilibrium statistical mechanics, there exist simple models that are helpful in capturing interesting experimental facts. A primary interest in the area of active matter is in the understanding of fundamental aspects of nonequilibrium-phase transitions. Studies along this direction are motivated by observations of structures and dynamics in assemblies like a colony of bacteria or a flock of birds, [1,27] resembling those concerning phase transitions in passive matter systems. Model dynamical systems having Vicsek-like simple velocity alignment rules or possessing active Brownian particles (ABP) as constituents have been useful in realizing many of the observed structural and dynamical features spanning wide scales of length and time. In the passive case anomalous behavior of various thermodynamic and transport properties, [28,38,42,44] upon approach of the state point toward the criticality, have been quantified experimentally and are captured by combinations of analytical theories and computer simulations. A major drive in this area has been in the understanding of universality in the exponents of power-law singularities. Analogous questions have been asked in the context of kinetics of phase transitions as well. In this area, following quench of a homogeneous system, inside the coexistence region, as the new equilibrium is approached, investigations have focused on learning universality in the evolution dynamics. There the primary interest has been in the exponent for the power-law time dependence of average size of domains that are either rich or poor in constituents of a specific type. Among other interests in this sub-branch two important ones are in understanding scaling properties associated with pattern and aging in the coarsening systems. Both critical and coarsening phenomena are of importance in the active matter context as well and have been receiving attention. In critical phenomena there exist debates on universality. Unlike for the passive systems here the universality may be weak and different types of transport, e.g., presence or absence of hydrodynamic interactions, [40,45] may change critical properties that will remain unaltere
活性物质系统是由自推进粒子组成的,为研究非平衡现象提供了理想的基础。这种自我推进是通过不断地从单粒子尺度的环境中汲取能量来提供燃料的。这种系统的例子很常见,覆盖范围很广,从分子水平的生物系统到大型动物社会。然而,这些成分不一定只能是有生命的物体。这些系统经常表现出迷人的模式和动态。从基础和实践的角度来看,理解这种集体现象都很重要。尽管存在概念上的困难[4-7],例如,关于温度的定义,在理论层面上已经取得了重大进展。在非平衡统计力学领域,存在一些简单的模型,有助于捕捉有趣的实验事实。在活性物质领域的主要兴趣在于理解非平衡相变的基本方面。沿着这一方向的研究是由对细菌群体或鸟群等群体的结构和动力学观察所激发的,[1,27]类似于对被动物质系统相变的研究。具有类似维塞克的简单速度对准规则或具有活性布朗粒子(ABP)作为组成部分的模型动力系统在实现许多已观察到的跨越大尺度长度和时间的结构和动力学特征方面是有用的。在被动情况下,各种热力学和输运性质的异常行为,[28,38,42,44]在接近临界状态点时,已经通过实验量化,并通过分析理论和计算机模拟的结合来捕获。这个领域的一个主要推动力是对幂律奇点指数的普适性的理解。在相变动力学中也提出了类似的问题。在这一领域,随着同质系统的猝灭,在共存区域内,随着新的平衡的接近,研究的重点是学习进化动力学中的普遍性。在那里,主要的兴趣是指数的幂律时间依赖于域的平均大小,这些域在特定类型的成分中要么丰富,要么贫乏。在这个分支的其他兴趣中,两个重要的是理解与粗化系统中模式和老化相关的尺度特性。临界现象和粗化现象在活性物质环境中也很重要,并一直受到人们的关注。在批判现象中存在着关于普遍性的争论。与被动系统不同的是,这里的普遍性可能很弱,不同类型的输运,例如存在或不存在流体动力相互作用[40,45],可能会改变被动情况下保持不变的关键性质。这类系统中的粗化现象直到最近才开始得到系统的关注。除了与相变有关的方面之外,重要的是要了解在不同环境条件下,甚至在相图的正常区域,在稳态情况下的结构和动力学特性。这个特刊包含理论文章,通过利用最先进的分析和计算技术,解决属于这两个类别的问题。除了具有基本性质外,其中一些贡献具有很强的实际重要性。Binder和Virnau的“透视”文章对相变和普适性进行了很好的讨论。这些作者介绍了关键现象,以及动力学的相变,从现代
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引用次数: 0
Effect of Poiseuille flow on the dynamics of active vesicle 泊泽维尔流对活性囊泡动力学的影响
IF 1.2 4区 材料科学 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2021-06-30 DOI: 10.1080/1539445X.2021.1937222
Prabha Chuphal, S. Sahoo, S. Thakur
ABSTRACT The influence of an external flow on the dynamics of active deformable particles demands a detailed understanding of the involved mechanism due to their prominent applications in medical and industrial fields. In this regard, we have investigated the effect of an external Poiseuille flow on the motion of an active deformable vesicle using a hybrid coarse-grained computational method. The activity of the vesicle is maintained through the concentration gradient of the solvent across its surface. Such a deformable active object, when exposed to the Poiseuille flow, exhibits a range of dynamical modes, which are greatly influenced by the size of the vesicle. For smaller external flow strength, we have observed the competition between propulsion force and external flow for various vesicle sizes. An interesting tank-treading motion is found for stronger flow strength in the case of a large vesicle. With appropriate physical quantification, we have explained that the key factors affecting the translational and rotational motions of the vesicle are its surface fluidity and its resistance to the external flow.
外部流动对活性可变形颗粒动力学的影响,由于其在医疗和工业领域的突出应用,需要详细了解所涉及的机制。在这方面,我们使用混合粗粒度计算方法研究了外部泊泽维尔流对活动可变形囊泡运动的影响。囊泡的活性是通过溶剂在其表面的浓度梯度来维持的。这种可变形的活动物体,当暴露于泊泽维尔流时,表现出一系列动力学模式,这些模式受囊泡大小的极大影响。对于较小的外流强度,我们观察到不同囊泡大小的推进力和外流之间的竞争。在大泡的情况下,发现了一个有趣的槽踏运动,以增强流动强度。通过适当的物理量化,我们解释了影响囊泡平移和旋转运动的关键因素是其表面流动性和对外部流动的阻力。
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引用次数: 3
Synthesis of carboxymethyl Xanthan/ double-walled carbon nanotube hybrid hydrogel nanocomposite for transdermal release of drug 羧甲基黄原胶/双壁碳纳米管杂化水凝胶纳米复合材料的合成
IF 1.2 4区 材料科学 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2021-06-25 DOI: 10.1080/1539445X.2021.1943682
Maroua Stasaid, K. Boutemak, Lahcene Ibtissem, E. Flahaut, Amel Hadj-Ziane- Zafour
ABSTRACT The inclusion of double-walled carbon nanotubes in carboxymethyl xanthan-based hydrogels was developed in order to improve both mechanical and drug release (diclofenac) properties of these nanocomposites for potential application in the biomedical field. The synthesis of carboxymethyl xanthan was carried out by an esterification reaction between xanthan gum and monochloroacetic acid, and the grafting was confirmed by FTIR analysis. The obtained carboxymethyl derivatives exhibited higher hydrophilicity degrees of substitution compared to the native xanthan gum. The nanocomposites prepared using either raw or modified xanthan gum were characterized in terms of physical properties, and we evidenced both an increase in viscoelasticity by one order of magnitude and an improved distribution of the nanotubes within the hydrogel matrix in the case of the carboxymethyl xanthan. The trapping efficiency of diclofenac was improved by the addition of the nanotubes, reaching up to 74 wt %. While the nanotubes also allowed a slower release of the molecule. An in-vitro study was carried out to ensure that the CNTs grafted onto the modified CMX were not released during the diffusion of the active ingredient.
摘要在羧甲基黄原胶基水凝胶中加入双壁碳纳米管,以改善这些纳米复合材料的机械性能和药物释放(双氯芬酸)性能,从而在生物医学领域具有潜在的应用前景。通过黄原胶与一氯乙酸的酯化反应合成了羧甲基黄原胶,并通过FTIR分析证实了接枝反应。与天然黄原胶相比,所获得的羧甲基衍生物表现出更高的亲水取代度。使用生的或改性的黄原胶制备的纳米复合材料在物理性能方面进行了表征,我们证明了在羧甲基黄原胶的情况下,粘弹性增加了一个数量级,纳米管在水凝胶基质中的分布也得到了改善。纳米管的加入提高了双氯芬酸的捕获效率,最高可达74wt%。同时纳米管也允许分子的缓慢释放。进行了一项体外研究,以确保接枝到改性CMX上的CNT在活性成分的扩散过程中不会释放。
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引用次数: 3
Formation and tribological properties of octacosanoic acid monomolecular Langmuir–Blodgett films 二十烷酸单分子Langmuir–Blodgett薄膜的形成及其摩擦学性能
IF 1.2 4区 材料科学 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2021-06-13 DOI: 10.1080/1539445X.2021.1933034
V. Akulova, A. Salamianski, I. Chishankov, V. Agabekov
ABSTRACT Tribological properties of monomolecular Langmuir–Blodgett (LB) films of octacosanoic acid (OCA) fabricated on silicon substrates by horizontal precipitation (HP) method are studied. The wear resistance of OCA coatings was studied and compared with the stability of both octadecanoic acid (OA) and octadecyltrichlorosilane (OTS) monolayers. It was found that OCA films increase the wear stability of silicon surfaces by 7.5 and 27 times as compared to OA and OTS monolayers, and reduce the coefficient of friction of an initial surface from 0.25 to 0.07. Monomolecular OCA films can be used for the protection of silicon micro-electro-mechanical systems from wear and friction.
研究了用水平沉淀法(HP)在硅衬底上制备的八碳酸(OCA)单分子Langmuir-Blodgett (LB)薄膜的摩擦学性能。研究了OCA涂层的耐磨性,并与十八烷酸(OA)单层膜和十八烷基三氯硅烷(OTS)单层膜的稳定性进行了比较。结果表明,OCA薄膜使硅表面的磨损稳定性比OA单层和OTS单层提高了7.5倍和27倍,并使初始表面的摩擦系数从0.25降低到0.07。单分子OCA薄膜可用于保护硅微机电系统免受磨损和摩擦。
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引用次数: 0
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Soft Materials
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