纤维素纳米晶体薄膜的制备与表征

讨论了两种新型纤维素纳米晶体(Cellulose nanocrystal,CNC)薄膜的制备方法:浸没法和旋涂法,并利用红外反射吸收光谱(Infrared reflection absorption spectroscopy,IRRAS)和原子力显微镜(Atomic force microscopy,AFM)对其进行表征。AFM高度图显示两种工艺制备的CNC薄膜均由棒状的CNC纳米颗粒交错叠加而成。实验结果显示,旋涂法制备的薄膜更加光滑,粗糙度RMS约为2.7 nm。由于带电颗粒间斥力的存在,浸没法制备的CNC膜厚度最大约为15 nm,而旋涂法可以得到更厚的CNC薄膜,其厚度可达50 nm以上。研究CNC悬浮液浓度与旋涂法CNC膜厚之间的关系后发现,可以通过改变CNC溶液的浓度对薄膜厚度进行控制。IRRAS结果也证实随着CNC悬浮液浓度的增加,旋涂薄膜的厚度随之增加。     

Nanocomposite structures of polypyrrole derivatives and poly (acrylonitrile‐co‐itaconic acid) produced by in situ polymerization as carbon nanofiber precursor

This study aimed to produce nanoparticles of poly (acrylonitrile‐co‐itaconic acid) (P (AN‐co‐IA)) containing conjugated polymers of pyrrole, N‐Methylpyrrole, 2,5‐dimethylpyrrole, and 1‐(Triisopropylsilyl)pyrrole which were synthesized by emulsion polymerization. Nanocomposite structures of P (AN‐co‐IA)/polypyrrole and polymer of pyrrole derivatives were produced via in situ polymerization, and the nanoparticle formation were followed by morphologic and ultraviolet‐visible (UV‐Vis) spectroscopic methods. Characterizations were made by Fourier transform infrared‐attenuated total reflectance (FTIR‐ATR) and Raman spectroscopy. Atomic force microscopy (AFM) was used for investigating the surface characteristics of the nanoparticles. Characterization results revealed that nanoparticles containing conjugated polymers had rougher surface than P (AN‐co‐IA) nanoparticles. It was also observed that the nanoparticles were well‐distributed although having some agglomerates. Moreover, depending on the type of monomer of conjugated polymer, the shape and size of the produced nanoparticles differed by conjunction with their polymerization rate. These findings can be used as a startup information for production of carbon nanofibers (CNFs) with desired properties after oxidation and carbonization, and as a high‐performance and cost‐effective flame and heat‐resistant material (oxidized copolymers of polyacrylonitrile nanofiber).     

Cooperativity of Catechols and Amines in High‐Performance Dry/Wet Adhesives

The outstanding adhesive performance of mussel byssal threads has inspired materials scientists over the past few decades. Exploiting the amino‐catechol synergy, polymeric pressure‐sensitive adhesives (PSAs) have now been synthesized by copolymerizing traditional PSA monomers, butyl acrylate and acrylic acid, with mussel‐inspired lysine‐ and aromatic‐rich monomers. The consequences of decoupling amino and catechol moieties from each other were compared (that is, incorporated as separate monomers) against a monomer architecture in which the catechol and amine were coupled together in a fixed orientation in the monomer side chain. Adhesion assays were used to probe performance at the molecular, microscopic, and macroscopic levels by a combination of AFM‐assisted force spectroscopy, peel and static shear adhesion. Coupling of catechols and amines in the same monomer side chain produced optimal cooperative effects in improving the macroscopic adhesion performance.     

Unlocking the Hidden Potential of Cosmetics Waste for Building Sustainable Green Pavements in the Future: A Case Study of Discarded Lipsticks

This investigation is dedicated to unlocking the hidden potential of discarded cosmetics towards building green sustainable road pavements in the future. It is particularly aiming at exploring waste lipstick (WLS) as a high-quality functional additive for advanced asphalt mix technologies. To fuel this novel innovation, the effect of various WLS doses (e.g., 5, 10, and 15 wt.%) on the performance of base AP-5 asphalt cement was studied in detail. A wide array of cutting-edge analytical lab techniques was employed to inspect in-depth the physicochemical, microstructural, thermo-morphological, and rheological properties of resultant admixtures including: elemental analysis, Fourier transform-infrared spectroscopy (FT-IR), X-ray diffraction (XRD), thin-layer chromatography-flame ionization detection (TLC-FID), scanning electron microscopy (SEM), atomic force microscopy (AFM), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), needle penetration, ring and ball softening point, Brookfield viscometer, ductility, and dynamic shear rheometer (DSR) tests. Unlike the unstable response of asphaltenes, the additive/artificial aging treatments increased the fraction of resins the most, and decreased that of aromatics; however, asphaltenes did not impair the saturates portion, according to Iatroscan research. FT-IR scan divulged that the WLS-asphalt interaction was physical rather than chemical. XRD diagnosis not only revealed an obvious correlation between the asphaltenes content and the fresh-binder crystallinity but also revealed the presence of fillers in the WLS, which may generate outstanding technical qualities to bituminous mixes. According to AFM/SEM analyses, the stepwise incorporation of WLS grew the magnitude of the “bee-shaped” microstructures and extended the roughness rate of unaged/aged binders. The prolonged consumption of the high thermal-stable additive caused a remarkable drop in the onset degradation and glass transition temperature of mixtures, thus enhancing their workability and low-temperature performance, according to TGA/DTGA/DSC data. The DSR and empirical rheological experiments demonstrated that the WLS could effectively lower the manufacturing and compaction temperatures of asphalt mixes and impart them with valuable anti-aging/fatigue-cracking assets. In a nutshell, the use of waste lipstick as an asphalt modifier is viable and cost-effective and could attenuate the pollution arisen from the beauty sector, while improving the performance of hot/warm asphalt mixes (HAM/WAM) and extending the service life of roadways.     

AFM关于压电陶瓷非线性效应的图像校正

在很多情况下,AFM图像的几何形貌都与实物存在差异的。本文主要针对压电陶瓷非线性引起的图像的失真,通过实验用标准DVD光盘对图像加以校正。希望用校正以后的软件,能尽可能获得样品的真实信息。     

聚(二甲基硅氧烷-co-甲氧基十二烷基硅氧烷)在棉纤维及其他模型表面的膜形貌及定向排列方式

用场发射扫描电镜(FESEM)、原子力显微镜(AFM)、光电子能谱(XPS)等仪器研究了棉纤维以及再生纤维素表面聚(二甲基硅氧烷-co-甲氧基十二烷基硅氧烷)(DDPS)的膜形貌及其定向排列方式.结果发现,在天然棉纤维以及再生纤维素模型表面,DDPS均能形成宏观上平滑、而微观形态学实则非均一的疏水性硅膜,表明DDPS的定向排列成膜方式为疏水性硅甲基、硅十二烷基朝外伸向空气,硅氧偶极键指向基质界面.     

X7R型MLCC流延瓷膜显微结构的AFM研究

片式电容是由电介质陶瓷薄膜和内电极相互重叠而成的多层独石结构,又称多层陶瓷电容器(mul-tilayer ceram ic capacitors,简称MLCC)。具有体积小、内部电感低、绝缘电阻高及漏电流小、介质损耗低、价廉等优点,被广泛应用于各种电子整机中的振荡、耦合、滤波和旁路电路,尤其是高     

多孔氧化铝薄膜的纳米结构和光谱特性研究

利用阳极氧化的方法制备出几种表面结构和尺度不同的多孔氧化铝薄膜,用原子力显微镜扫描获得了这些薄膜表面的纳米结构图像,并采用光谱仪测定了它们的反射光谱。实验表明,平均孔径为26和39 nm的多孔氧化铝薄膜表面具有独特的反射光谱,在500至1 000 nm波长范围内呈周期性地密集峰—谷分布,峰—谷的密集度或数量取决于薄膜表面纳米结构的尺度。讨论了纳米结构尺度与反射光谱之间的相互关系,并给出了适当的解释。     

NANOMECHANICAL MAPPING OF CARBON BLACK REINFORCED NATURAL RUBBER BY ATOMIC FORCE MICROSCOPY

Atomic force microscopy （AFM） has the advantage of obtaining mechanical properties as well as topographic information at the same time. By analyzing force-distance curves measured over two-dimensional area using Hertzian contact mechanics, Young＇s modulus mapping was obtained with nanometer-scale resolution. Furthermore, the sample deformation by the force exerted was also estimated from the force-distance curve analyses. We could thus reconstruct a real topographic image by incorporating apparent topographic image with deformation image. We applied this method to carbon black reinforced natural rubber to obtain Young＇s modulus distribution image together with reconstructed real topographic image. Then we were able to recognize three regions; rubber matrix, carbon black （or bound rubber） and intermediate regions. Though the existence of these regions had been investigated by pulsed nuclear magnetic resonance, this paper would be the first to report on the quantitative evaluation of the interfacial region in real space.     

金纳米粒子在氨基表面上的组装-pH值的影响

用原子力显微镜（AFM）和表面增强喇曼光谱（SERS）研究了pH值对金纳米粒子在Au／巯基苯胺自组装膜表面上组装效果的影响．AFM结果表明，金纳米粒子在表面上的覆盖度随pH值表现出规律性的变化，巯基苯胺自组装膜的SERS强度随pH值的变化也有类似的趋势．在磁性环境下，氨基未质子化，金粒子难以组装上，而在酸性条件下，氨基质子化带正电，金粒子与基底容易结合．我们认为金纳米粒子和氨基之间的作用属于静电力，pH值同时影响膜表面氨基的质子化程度和金纳米粒子表面的带电量．