短直链淀粉纳米颗粒涂层制备超亲水淀粉膜

采用蜡质玉米淀粉为原料,经普鲁兰酶脱支处理,制备短直链淀粉。将短直链淀粉糊化后的溶液,通过膜材浸泡的方式,使淀粉膜表面形成短直链淀粉涂层,再通过4℃的老化处理,制备超亲水淀粉膜。对超亲水淀粉膜的表面形貌、结晶结构、红外光谱及亲水性进行了研究。结果表明,短直链淀粉在淀粉膜表面自组装成了纳米颗粒结构,增加了膜材表面的粗糙度,改善了淀粉膜的亲水性能。当短直链淀粉溶液质量浓度为0.010 g/mL时,可获得水接触角接近于0°的超亲水淀粉膜。

High temperature frictional wear behaviors of nano-particle reinforced NiCoCrAlY cladded coatings

The NiCoCrAlY coatings strengthened by three nano-particles with the same addition were prepared on a Ni-base super alloy using laser cladding technique. The dry frictional wear behaviors of the coatings at 500 ℃ in static air were investigated. The comparison was made with the coating without nano-particles. The results show that the wear mechanism of the NiCoCrAlY coatings with nano-particles, like the coating without nano-particles, is the delamination wear due to the strong plastic deformation and oxidative wear. However, the frictional coefficient of the coatings increases and presents the decrease trend with the increase of sliding distance after adding nano-particles. Moreover, the wear rate of the coatings with nano-particles is only 34.0%-64.5% of the coating without nano-particles. Among the three nano-particles, the improvement of nano-SiC on the high temperature wear resistance of the coating is the most significant.

基于三维微结构的微流控芯片

微流控领域自二十世纪末诞生以来,凭借其高效率、低消耗的技术优势,在生命科学、化学合成和环境监测等领域显示出了巨大的应用前景。为了改良微流控芯片的进一步作用,使得优势更加明显,对微流控芯片沟道内表面进行改造,在沟道的内表面构筑一些纳米结构。该文研究的主要内容是在有抗腐蚀涂层的情况下,玻璃刻蚀液对玻璃在不同的时间下所刻蚀出的三维结构的区别,即纳米结构的尺寸差异。不同尺寸的纳米结构对细胞的富集能力不同,找出最适合的三维结构并制作出微流控芯片。结果表明在有纳米结构修饰比没有纳米结构修饰的微流控芯片对细胞富集效率高。

CeO2/Zn NANOCOMPOSITE COATING BY ELECTRODEPOSITION

The nanocomposite coating is obtained by electrochemical deposition of the zinc plating solution with ceria nanoparticles (mean diameter 30 nm). The effect of ceria nanoparticles on the electrodeposited zinc coating is stu died by weight loss test, inductively copuled plasma quantometer (ICP), scanning electron microscopy (SEM) and X ray diffraction (XRD), respectively. It is found that under the same electrodeposition conditions, the corrosion resistance of the nanocomposite coating increases obviously while that of the micron composite coating only improves slightly; The ceria content of the nanocomposite coating is more than that of the micron composite coating. Ceria nanoparticles modify the surface morphology and crystal structure of the zinc matrix in correlation with the increase of corrosion resistance.

Fabrication of Poly（y-glutamic acid）-coated Fe3O4 Magnetic Nanoparticles and Their Application in Heavy Metal Removal

In this study, poly（y-glutamic acid）-coated Fe3O4 magnetic nanoparticles （y-PGA/Fe304 MNPs） were successfully fabricated using the co-precipitation method. Fe3O4 MNPs were also prepared for comparison. The av erage size and specific surface area results reveal that 7-PGA/Fe304 MNPs （52.4 nm, 88.41 m2.g-1） have smaller particle size and larger specific surface area_ than Fe3O4 MNPs （62.0 nm, 76.83 mLg-1）. The y-PGA/Fe3O4 MNPs

Characterization of self-assembled nano-phase silane-based particle coating

Self-assembled nano-phase silane-based particle coating was prepared through sol-gel technique.Tetramethoxysilane and 3-glycidoxypropyltrimethoxysilane were used as precursors for the self-assembled sol-gel coatings.The silane colloidal particle size was analyzed by laser particle size measurement.The results indicate that the particle size is in nano-scale and the diameter of particles deceases with increasing dilution times.Gel permeation chromatography proves that the relative molecular mass of macromolecule in a referenced sol solution is 1220-1240 amu.A simulation model was proposed to study the siloxane structure.Fourier transform infrared spectra of solution and film prove the disappearing of epoxy bond.The results of solid-state 13C and 29Si nuclear magnetic resonance experiments indicate the formation of Si-O-Si network.Potentiodynamic analysis shows that the self-assembled coating has excellent corrosion resistance.Salt fog tests prove that 2-methyl piperidine as inhibitor significantly improves the corrosion resistance of the self-assembled coating.

In-situ characterization of metal nanoparticles and their organic coatings using laser-vaporization aerosol mass spectrometry

The development of methods to produce nanoparticles with unique properties via the aerosol route is progressing rapidly. Typical characterization techniques extract particles from the synthesis process for subsequent offiine analysis, which may alter the particle characteristics. In this work, we use laser-vaporization aerosol mass spectrometry （LV-AMS） with 70-eV electron ionization for real-time, in-situ nanoparticle characterization. The particle characteristics are examined for various aerosol synthesis methods, degrees of sintering, and for controlled condensation of organic material to simulate surface coating/functionalization. The LV-AMS is used to characterize several types of metal nanoparticles （Ag, Au, Pd, PdAg, Fe, Ni, and Cu）. The degree of oxidation of the Fe and Ni nanoparticles is found to increase with increased sintering temperature, while the surface organic-impurity content of the metal particles decreases with increased sintering temperature. For aggregate metal particles, the organic-impurity content is found to be similar to that of a monolayer. By comparing different equivalent-diameter measurements, we demonstrate that the LV-AMS can be used in tandem with a differential mobility analyzer to determine the compactness of synthesized metal particles, both during sintering and during material addition for surface functionalization. Further, materials supplied to the particle production line downstream of the particle generators are found to reach the generators as contaminants. The capacity for such in-situ observations is important, as it facilitates rapid response to undesired behavior within the particle production process. This study demonstrates the utility of real-time, in-situ aerosol mass spectrometric measurements to characterize metal nanoparticles obtained directly from the synthesis process line, including their chemical composition, shape, and contamination, providing the potential for effective optimization of process operating parameters.

Organic coating of 1-2-nm-size silicon nanoparticles： Effect on particle properties

Photoluminescent silicon nanoparticles 1-2 nm in size were synthesized by a wet chemical procedure and derivatized with propylamine （NH2SiNP）. Surface NH2 groups were used as linkers for additional poly（ethylene glycol） （PEG） and folic acid （Fo） attachment （PEG-NHSiNP and Fo-NHSiNP, respectively） to enable efficient targeting of the particles to tumors and inflammatory sites. The particles were characterized by transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, ζ potential, dynamic light scattering, and time-resolved anisotropy. The photophysical properties and photosensitizing capacity of the particles and their interaction with proteins was dependent on the nature of the attached molecules. While PEG attachment did not alter the photophysical behavior of NH2SiNP, the attachment of Fo diminished particle photoluminescence. Particles retained the capacity for 1O2 generation; however, efficient 1O2 quenching by the attached surface groups may be a drawback when using these particles as 1O2photosensitizers. In addition, Fo attachment provided particles with the capacity to generate the superoxide anion radical （O2-）. The particles were able to bind tryptophan residues of bovine serum albumin （BSA） within quenching distances. NH2SiNP and PEG-NHSLNP ground state complexes with BSA showed binding constants of （3.1 ± 0.3） × 10^4 and （1.3 ±0.4） × 10^3 M-1, respectively. The lower value observed for PEG-NHSiNP complexes indicates that surface PEGylation leads to a reduction in protein adsorption, which is required to prevent opsonization. An increase in particle luminescence upon BSA binding was attributed to the hydrophobic environment generated by the protein. NH2SiNP-BSA complexes were also capable of resonance energy transfer.