Preparation and spectral analysis of gold nanoparticles using magnetron sputtering and thermal annealing

Gold(Au) nanoparticles were prepared on Au-fi lm-coated K9 glass and silicon substrates by direct current(DC) magnetron sputtering and thermal annealing treatment. The effects of substrate material, annealing temperature, and time on morphologies of Au nanoparticles were investigated, and the formation mechanism of Au nanoparticles was discussed. The experimental results indicate that silicon substrate is more suitable for the formation of Au nanoparticles. On a silicon substrate, Au nanoparticles formed with good spherical shapes at temperature over 700 ℃. It was also found by spectral analysis that the fi eld enhancement factor of the island-shaped Au particles was smaller than that of the granular Au particles; the better the spherical shape as well as the smaller the size and spacing of Au particles, the higher the light absorption rate; the absorption peak had a red shift with increasing particle size and spacing.     

PLD preparation of GeS6 amorphous film and investigation on its photo-induced darkening phenomenon

GeS6 chalcogenide amorphous fi lm was deposited on glass substrate via PLD（pulsed laser deposition） technique. The performance and structure of the fi lm was characterized by XRD（X-ray diffraction）, SEM（Scanning Electron Microscopy）, EDS（Energy Dispersive Spectroscopy）, optical transmission spectra, and Raman spectra, etc. The GeS6 amorphous fi lm was irradiated by 532 nm linearly polarized light, and its photoinduced darkening was investigated. The results showed that the GeS6 chalcogenide amorphous fi lm was smooth and compact with uniform thickness and combined with the substrate fi rmly, and its chemical composition was in consistency with the bulky target. When laser energy was fi xed, the transparence of the fi lm declined with the increase of the laser irradiation time. Obvious photo-induced darkening and relaxation phenomenon of the fi lm after laser irradiation were observed in this investigation.     

Effect of Mg-film thickness on the formation of semiconductor Mg2Si films prepared by resistive thermal evaporation method

Mg fi lms of various thicknesses were deposited on Si(111) substrates at room temperature by resistive thermal evaporation method, and then the Mg/Si samples were annealed at 40 ℃ for 4 h. The effects of Mg fi lm thickness on the formation and structure of Mg2Si fi lms were investigated. The results showed that the crystallization quality of Mg2Si fi lms was strongly infl uenced by the thickness of Mg fi lm. The XRD peak intensity of Mg2Si(220) gradually increased initially and then decreased with increasing Mg fi lm thickness. The XRD peak intensity of Mg2Si(220) reached its maximum when the Mg fi lm of 380 nm was used. The thickness of the Mg2Si fi lm annealed at 400 ℃ for 4 h was approximately 3 times of the Mg fi lm.     

Preparation and properties of PMMA modified silica aerogels from diatomite

Diatomite was used as raw material to prepare sodium silicate with a modulus of 3.1 by alkalidissolution method and the resulted sodium silicate solution was employed as a precursor. Methyl methacrylate monomers were introduced in wet gels through solution-immersion, and upon heating at 70 ℃, the mesoporous surfaces throughout the skeletal framework were coated with the polymer layer. PMMA modified silica aerogels were successfully synthesized via ambient pressure drying. The properties were investigated by FTIR, NMR, TGA, nitrogen adsorption-desorption, FESEM and nano-indentation, etc. Results indicate that with the increasing of PMMA incorporated into silica aerogels, the bulk density and the BET surface area increase, the porosity decreases. Through the observation of FESEM, it is found that the interconnecting pores and the big pores add, the pore size distribution expands from 5-17 to 28-150 nm. By comparison, the PMMA modified silica aerogels achieve a 52-fold increase in hardness and a 10-fold increase in modulus.     

高效除硅性能的改性膨润土制备工艺优化

以钠基膨润土为原料,通过添加铝盐为改性剂,制备出了一种新型高效绿液除硅剂,其硅吸附效率最高可达90%左右.并以竹浆绿液的硅吸附率和pH变化为标准,研究了该种改性膨润土的制备工艺.其最佳工艺条件为:钠基膨润土与铝盐的质量比为1∶4;添加顺序先将钠基膨润土与水混合,再加入铝盐,加水量为66mL/1g钠基膨润土;搅拌时间为2h,搅拌速率为1 200r/min;反应温度为室温,静置分离12h,105℃干燥,研磨,过200目筛.     

纳豆芽孢杆菌菌剂的制备工艺

采用单因素及正交试验对纳豆芽孢杆菌发酵培养基、pH、温度、发酵时间等条件进行了考察,利用喷雾干燥法制备菌剂,考察了β-环糊精、蔗糖、可溶性淀粉及脱脂奶粉作为保护剂对菌剂制备的影响,并研究了储藏时间及条件对菌剂发酵活力的影响.研究结果表明:纳豆芽孢杆菌发酵培养基为黄豆浸汁培养基:黄豆以5倍水体积浸泡8~14h,121℃~126℃,0.1~0.15MPa处理1h,滤除黄豆,取豆水,加入5%的葡萄糖和0.02%的K2HPO4,调节pH至7.0;最优发酵工艺:初始pH7.0,37℃发酵10h;喷雾干燥最佳保护剂为5%脱脂奶粉;菌剂4℃冷藏180d以内不影响发酵活力.上述工艺下所制得的纳豆芽孢杆菌菌剂活菌数为6.5×108 CFU/g,发酵生产纳豆激酶性能良好.发酵生产纳豆激酶酶活为2 000~2 200IU/g.本研究为纳豆芽孢杆菌菌剂制备提供了一条较为合理的工艺路线.     

Preparation and characterization of PEGDE crosslinked silk fibroin film

To obtain water-insoluble silk fibroin(SF) materials, polyethylene glycol diglycidyl ether(PEG-DE) was selected as a crosslinking agent to prepare SF films(blends). The reaction conditions were optimized for the crosslinking of the SF molecules. The hot water stability of the blends was measured using BCA protein assay and gravimetric analysis. The molecular conformation and crystalline structure of the blends were analyzed by FTIR and XRD, respectively. When the mass ratio of SF:PEG-DE was 1.0:0.8, the hot water loss rate of the SF blends was minimized. PEG-DE could induce SF molecules to form β-sheets during the gel reaction process, resulting in improved crystallinity and hot water dissolved resistance of the blend films. In order to demonstrate the cytotoxicity of the chemical reagents used to crosslink SF, L929 cells were seeded on the blend film(SF:PEG-DE = 1:1) and cultured for 3 days. Cells of L929 readily adhered and spread in the fusiform on the blend film resulting in high cell viability. The extracted liquid from the SF porous film did not inhibit cell proliferation, as estimated by the MTT assay.     

我校获得四项2015年度上海市自然科学基金项目资助

<正>日前,经上海市科委组织专家网上评审、见面会考评等评选程序,我校有四位老师获得该项目资助。获得资助的分别为工学部关杰老师的"废弃液晶与PVC塑料协同氯化热解气化机理与制备高纯铟材料的研究"、孙志国老师的"腐植酸盐和电石渣固存工业废气中CO2的耦合机制研究"、薛建新老师的"无限状态并发进程的等价关系验证问题研究"和杨丹丹老师的"新型高储能密度介电材料制备及其结构与性能的关联研究"。项目期为三年,资助力度为10万元/项。     

Surface resistivity of carbonaceous fiber/PTFE antistatic coatings

Abstract： PAN （Polyacrylonitrile）-based carbonaceous fibers were prepared at the heat treatment temperature （HTT） range of 650 to 900 ℃. The relationships among HTT, carbon content and volume resistivity of the carbonaceous fibers were investigated. The carbonaceous fibers/PTFE （Polytetrafluoroethylene） antistatic coatings were prepared by the spraying technology and the effects of carbonaceous fibers and pigments on surface resistivity of the coatings were systematically discussed. Micrographs provide insight into the antistatic mechanism of the coating. The results show that carbon content of the carbonaceous fibers increases from 68.8% to 74.8% （mass fraction） and the volume resistivity decreases drastically from 1.94× 10^-3 to 8.27× 10 ^-2.cm. The surface resistivity of the antistatic coating is adjustable between 10^5 and 10^8Ω2 to fit the different antistatic materials. Static is dissipated by a conductive network of short fibers and the tunneling effect between the neighboring fibers and conductive pigments. Conductive pigments make the conductive network more perfect and improve the antistatic ability, but insulating pigments acting as barriers for the formation of conductive channel increases the surface resistivity of the coatings. The influence of pigments on the surface resistivity drops gradually with the decrease of the carbonaceous fibers volume resistivity.     

×Synergistic action of non-solvent induced phase separation in preparation of poly（vinyl butyral） hollow fiber membrane via thermally induced phase separation

A systematic study of air gap distance effects on the structure and properties of poly（vinyl butyral） hollow fiber membrane via thermally induced phase separation （TIPS） has been carried out. The results show that the hollow fiber membrane prepared at air gap zero has no skin layer; the pore size near the outer surface is larger than that near the inner surface; and the special pore channel-like structure near the outer surface is formed, which is quite different with the typical sponge-like structure caused by TIPS and the finger-like structure caused by non-solvent induced phase separation （NIPS）, because of the synergistic action of non-solvent induced phase separation at air gap zero. The pore size gradually decreases from outer surface layer to the intermediate layer, but increases gradually from intermediate layer to the inner surface layer. With the increase of air gap distance, the pore size near the outer surface gets smaller and a dense skin layer is formed, and the pore size gradually increases from the outer surface layer to the inner surface layer. Water permeability of the hollow fiber membrane decreases with air gap distance, the water permeability decreases sharply from 45.50× 10^-7 to 4.52× 10^-7 m^3/（m^2-s.kPa） as air gap increases from 0 to 10 mm at take-up speed of 0.236 m/s, further decreases from 4.52×10^-7 to 1.00×10 ^-8m^3/（m^2.s·kPa） as the air gap increases from 10 to 40 mm. Both the breaking strength and the elongation increase with the increase of air gap distance. The breaking strength increases from 2.25 MPa to 4.19 MPa and the elongation increases from 33.9% to 132.6% as air gap increases from 0 mm to 40 mm at take-up speed 0.236 m/s.