紫外/臭氧复合杀灭水中细菌性能研究

为开发一种高效灭菌方法,研究了UV/O3的复合灭菌性能,对紫外辐射、臭氧和羟基自由基等在体系中的各自作用进行探讨,同时考察pH值、温度等对灭菌效果的影响.结果表明,UV/O3较单独紫外或臭氧灭菌时效果有所提高,在初始臭氧质量浓度为5.02mg·L-1,液面紫外辐射强度为6.5mW·cm-2,灭菌时间1.5～9.0s时,UV/O3对细菌总数灭菌率达3.6～6.4,单独紫外时为1.8～4.7,单独臭氧时仅为1.6～3.0.羟基自由基的产生是复合灭菌效果增加的主要原因.随紫外辐射强度和臭氧投加量的增加,复合灭菌作用得到提高.pH值在5.5～8.5变化时,UV/O3灭菌效果随原水pH值的增加略有提高.温度由10℃上升到27℃时,灭菌效果稍有下降.由此可见,UV/O3是一种高效可行的水体灭菌技术。     

微波辐射提取桔皮中橙皮苷的研究

以乙醇溶液为提取溶剂,采用微波辐射提取桔皮中的橙皮苷,考察了溶剂浓度、微波功率、微波辐射时间、液料比等因素对橙皮苷提取量的影响.正交试验优化显示：溶剂体积浓度55%、微波提取功率400 W、辐射时间70 s和液料之比15∶1（质量比）时,橙皮苷的提取率为41.05%,比无微波辐射提取提高了14.21%.     

Physical properties of electron beam irradiated poly(vinyl butyral) composites with carbamate,imidazole, and tetrazolium dye

Films of poly(vinyl butyral) composites with triphenyl tetrazolium chloride dye (TTC) and the antioxidant nickel dibutyl dithiocarbamate (NBC) or 2‐mercaptobenzimidazole (MBI) were prepared by the solution casting method using butyl alcohol as a solvent. The effect of various doses of electron beam irradiation (50–200 kGy) on color response, thermal, and mechanical properties were investigated. The color measurements showed that the films of the different composites possessed a high sensitivity to electron beam irradiation, in which the nearly colorless films were changed to deep red color, which can be easily detected by visual observations. In addition, the change in color depends on irradiation dose and the contents of the TTC dye. Moreover, the presence of the antioxidants NBC or MBI has no effect on the development of color. However, PVB/TTC and PVB/TTC/MBI composites showed high regular change in color as a function of irradiation dose. The thermogravimetric analysis used to study the thermal stability indicated that PVB/TTC composites either before or after electron beam irradiation are thermally more stable than neat PVB polymer. The presence of the antioxidants NBC or MBI offered protection to PVB/TTC composites against decomposition or oxidative degradation resulted from irradiation. Blending unirradiated PVB with TTC dye, mixture of TTC and NBC, and mixture of TTC and MBI reduced the tensile strength by 4, 20, and 17% upon blending, respectively. However, the reduction in tensile strength of the entire composite films (～7% based on the initial value) upon exposure to a dose of 50 kGy is acceptable for practical applications. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 4358–4365, 2006     

Microstructure evolution in Si+ ion irradiated and annealed Ti3SiC2 MAX phase

Ti₃SiC₂ samples were irradiated by a 6-MeV Si⁺ ion to a fluence of 2 $\times$ 10¹⁶ Si⁺ ions/cm² at 300°C followed by annealing at 900°C for 5 h. A transmission electron microscope was used to characterize microstructural evolution. The phase of Ti₃SiC₂ transformed from the hexagonal close-packed (HCP) to a face-centered cubic structure after irradiation. Hexagonal screw dislocation networks were identified at the deepest position of the irradiated area, which are the products of dislocations reactions. After annealing, the irradiated region has reverted to the original HCP structure. High-density cavities and stacking faults were formed along the basal planes. In addition, ripplocations have been observed in the irradiated region in the Ti₃SiC₂ sample after annealing. Our insights into the formation processes and corresponding mechanisms of these defect structures might be helpful in the material design of advanced irradiation tolerance materials.     

Biodegradation of low‐density polyethylene/thermoplastic starch foams before and after electron beam irradiation

Foamy low‐density polyethylene/plasticized starch (LDPE/PLST) blends at different compositions were produced in the presence of azodicarbonamide (ACA) compound as foaming agent. The LDPE/PLST blends before and after electron beam irradiation were investigated in terms of mechanical properties, bulk density, and structure morphology. Moreover, the biodegradability of these materials was evaluated by the soil burial test for 2 months, in which the buried sheets were also examined by scanning electron microscopy (SEM). The results showed that the increase of PLST content from 24 to 30% was accompanied by a decrease in the yield and break stresses of 10 and 20% for the unirradiated blends without the foaming agent, respectively. Further decrease in these mechanical parameters was observed after the foaming process. The bulk density, void fraction, cell size measurements as well as the examination by SEM illustrate clearly the cell growth of the foam structure. The soil burial test and SEM micrographs indicate the growth of microorganisms overall the blend sheets and that the blend was completely damaged after two months of burying. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Photocatalytic behavior of TiO_2 and ZnO prepared with different methods under ultraviolet and visible light irradiation

IntroductionIn recent years photocatalytic oxidation hasreceived considerable attention as an alternativeremediation technology since the method offers anumber of advantages over conventionaltechnologies [1,2] Elimination o…     

微波辐射下NKC-9树脂催化合成1-萘乙酸甲酯

以NKC-9阳离子交换树脂为催化剂,在微波条件下用1-萘乙酸和甲醇合成1-萘乙酸甲酯.最佳合成条件为:醇酸摩尔比为14:1,催化剂为1-萘乙酸的80%,微波辐射时间为15分钟,微波功率为600瓦,产率为80.48%.     

Annealing effects on the structure and hardness of helium-irradiated Cr2AlC thin films

Cr₂AlC MAX phase thin films prepared by radio-frequency magnetron sputtering were irradiated at room temperature by 100 keV helium ions to a fluence of 1 × 10¹⁷ ions cm⁻². The effects of thermal annealing on the structural and mechanical properties of the helium-irradiated Cr₂AlC films as well as the helium release were investigated by grazing-incidence X-ray diffraction (GIXRD), Raman spectroscopy, and scanning electron microscope (SEM) in combination with nano-indentation and elastic recoil detection (ERD) analysis. The irradiation-induced structural damage in the Cr₂AlC is significantly recovered by thermal annealing at temperatures around 600℃, attributed to high defect diffusivity. After annealing to 750℃, the hardness of irradiated films recovered almost completely, which is ascribes to both defect recombination and reformation of damaged chemical bonds. Substantial helium release occurring at this annealing temperature is closely related to the damage recovery due to helium irradiation.     

Transmission electron microscopy study of extended defect evolution and amorphization in SiC under Si ion irradiation

The damage induced in 3C-SiC epilayers on a silicon wafer by 2.3-MeV Si ion irradiation for fluences of 10¹⁴, 10¹⁵, and 10¹⁶ cm⁻², was studied by conventional and high-resolution transmission electron microscopy (TEM/HRTEM). The evolution of extended defects and lattice disorder is followed in both the 3C-SiC film and Si substrate as a function of ion fluence, with reference to previous FTIR spectroscopy data. The likelihood of athermal unfaulting of native stacking faults by point defect migration to the native stacking faults is discussed in relation to damage recovery. Threshold energy densities and irradiation doses for dislocation loop formation and amorphous phase transformation are deduced from the damage depth profile by nuclear collisions. The role of electronic excitations on the damage recovery at high fluence is also addressed for both SiC and Si.     

Radiation crosslinking of linear polyethyleneimine-based nanoparticles grafted to poly(glycidyl methacrylate) via trimethylolpropane triacrylate as potential electronic packaging material

Linear polyethyleneimine (L-PEI)-based nanoparticles were synthesized via hydrolysis of poly-2-methyl-2-oxazoline (PMeOx), which was prepared by cationic ring-opening polymerization of the oxazoline five-membered ring. Herein, a kinetic study of the ring-opening polymerization reaction is discussed. The nuclear magnetic resonance spectrum of PMeOx verified the presence of repeating units and terminal groups in the polymer's structure. Molar ratios of PEI and PMeOx were characterized using size exclusion chromatography with low-polydispersity polymer chains as the controlled polymerization reaction. PEI and PMeOx exhibited narrow particle size distribution with hydrodynamic radii of 89 and 67 nm, respectively, as determined via dynamic light scattering analysis. In addition, atomic forces and scanning electron microscopy were used to investigate the topography of the PEI thin films. Poly(glycidyl methacrylate) P(GMA) was grafted onto a PEI chain in the presence of trimethylolpropane triacrylate (TMPTA) as the crosslinking agent to synthesize the P(GMA–PEI–TMPTA) tripolymer via free radical polymerization using gamma irradiation. The thermal characterization of the P(GMA–PEI–TMPTA) tripolymer was conducted using thermogravimetric analysis and differential scanning calorimeter. Generally, the thermal stability of the P(GMA–PEI–TMPTA) tripolymer was improved at low-glycidyl methacrylate concentrations. The prepared tripolymer could be used as effective packaging materials for electronics industries.