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101.
实验研究了大模面积光子晶体光纤飞秒激光器在近零色散点展宽脉冲锁模的束缚态运转.获得了双脉冲束缚态锁模,以及脉冲间隔不相等的多脉冲束缚态锁模,实验发现束缚态的子脉冲间距具有随机性.通过建立光纤锁模激光器的数值模型,分析了激光器束缚态锁模建立的动力学过程,在一定抽运强度下,激光器存在多个稳态,或者单脉冲运转,或者子脉冲间隔不相等的束缚态运转,这取决于锁模建立阶段半导体可饱和吸收镜(SESAM)对噪声信号的随机提取.并提出了抑制束缚态的方法,模拟得出此项技术可直接获得的最大单脉冲能量为19.6 nJ,考虑到40%左右的压缩损耗,可得到压缩至76 fs的最短脉冲,单脉冲能量为11.8 nJ.数值模拟结果能很好的与实验相符合. 相似文献
102.
Xueyu Qiu Yadong Han Xiuli Zhuang Xuesi Chen Yuesheng Li Xiabin Jing 《Journal of nanoparticle research》2007,9(5):901-908
Nano-hydroxyapatite (HA)/poly(l-lactide) (PLLA) composite microspheres with relatively uniform size distribution were prepared by a solid-in-oil-in-water
(s/o/w) emusion solvent evaporation method. The encapsulation of the HA nanopaticles in microshperes was significantly improved
by grafting PLLA on the surface of the HA nanoparticles (p-HA) during emulsion process. This procedure gave a possibility
to obtain p-HA/PLLA composite microspheres with uniform morphology and the encapsulated p-HA nanoparticle loading reached
up to 40 wt% (33 wt% of pure HA) in the p-HA/PLLA composite microspheres. The microstructure of composite microspheres from
core-shell to single phase changed with the variation of p-HA to PLLA ratios. p-HA/PLLA composite microspheres with the diameter
range of 2–3 μm were obtained. The entrapment efficiency of p-HA in microspheres could high up to 90 wt% and that of HA was
only 13 wt%. Surface and bulk characterizations of the composite microspheres were performed by measurements such as wide
angle X-ray diffraction (WAXD), thermal gravimetric analysis (TGA), environmental scanning electron microscope (ESEM) and
transmission electron microscopy (TEM). 相似文献
103.
Shengkai Li Zhaotian Zhu Xinqi Cai Minghui Song Shen Wang Qing Hao Long Chen Zhuo Chen 《中国化学》2021,(6):1491-1497
Main observation and conclusion
Surface-enhanced Raman spectroscopy(SERS)-based bioanalytical technique involves the interaction of SERS-active substrate with c... 相似文献
104.
105.
Jie Song Eunji Lee Byoung‐Ki Cho 《Journal of polymer science. Part A, Polymer chemistry》2013,51(2):446-456
A well‐defined (PEO‐PS)2‐PLA miktoarm terpolymer ( 1 ) was synthesized by stepwise click reactions of individually prepared poly(ethylene oxide) (PEO), polystyrene (PS, polymerized by atom transfer radical polymerization), and polylactide (PLA, polymerized by ring‐opening polymerization) blocks. As characterized by differential scanning calorimetry and small‐angle X‐ray scattering techniques, the terpolymer self‐assembled into a hexagonal columnar structure consisting of PLA/PEO cylindrical cores surrounded by PS chains. In contrast, the ion‐doped sample ( 1‐Li+ ) with lithium concentration per ethylene oxide = 0.2 exhibited a three‐phase lamellar structure, which was attributed to the microphase separation between PEO and PLA blocks and to the conformational stabilization of the longest PLA chain. The two‐phase columnar morphology before the ion doping was used to prepare a nanoporous material. PLA chains in the cylindrical core region were hydrolyzed by sodium hydroxide, producing nanopores with a pore diameter of about 14 nm. The resulted nanoporous material sank to the bottom in water, because of water‐compatible PEO chains on the walls. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
106.
In this letter, we discuss the increase in the average cluster size by lowering the stagnation temperature of the methane (CH4) gas. The Coulomb explosion experiments are conducted to estimate the cluster size and the size distribution. The average CH4 cluster sizes Nay of 6 230 and 6 580 are acquired with the source conditions of 30 bars at 240 K and 60 bars at 296 K, respectively. Empirical estimation suggests a five-fold increase in the average size of the CH4 clusters at 240 K compared with that at room temperature under a backing pressure of 30 bars. A strong nonlinear Hagena parameter relation (Г^*∝ T0^-3.3) for the CH4 clusters is revealed. The results may be favorable for the production of large-sized clusters by using gases at low temperature and high back pressures. 相似文献
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110.
Pirita Rämänen Paavo A. Penttilä Kirsi Svedström Sirkka Liisa Maunu Ritva Serimaa 《Cellulose (London, England)》2012,19(3):901-912
Cellulose whiskers were prepared from wood- and cotton-based microcrystalline cellulose and dried by two methods: freeze-drying or air-drying. The effect of drying method on the properties and structure of the whiskers were studied. Furthermore, the influence of the source of cellulose on the nanoscale structure was investigated. Drying method was observed to slightly influence the thermal stability of cellulose whiskers, whereas the char residue varied significantly depending on the drying process performed. Small- and wide-angle X-ray scattering and solid state nuclear magnetic resonance spectroscopy were used to examine the crystallinity and nanoscale structure of the dried whiskers. It was observed that the crystal structure and crystallinity of cellulose whiskers remained during all treatments, whereas their nanoscale structure was significantly influenced by drying method, neutralization, and source of cellulose. Relationships between thermal behavior and nanoscale structure were reported and discussed. 相似文献