碳纳米纤维吸附储氢性能分析

文中综合碳纳米纤维微观结构的表征结果以及氢吸脱附等温线的实验测量结果,对碳纳米纤维的吸附储氢性能进行了综合分析,分析发现:比表面积和中孔容积均与氢吸附量成线性关系;微孔容积对材料吸附性能影响较大,微孔容积与氢吸附量成抛物线关系;氢在常温左右以及77K下的吸附等温线呈现超临界气体的吸附特征,氢在273K和353K下的吸脱附等温线也基本重合,呈现的是物理吸附的特征。实验结果还说明:常温左右,甚至是77K下,碳纳米纤维均不适合于氢的吸附储存。     

Band-rejection filter based on a Bragg fiber with a defect layer

<正>A novel band-rejection filter based on a Bragg fiber with a defect layer is proposed.A defect layer is introduced in the periodic high/low index layers in the cladding of the Bragg fiber,which results in large confinement loss for some resonant wavelengths inside the band gap range of the Bragg fiber.A segment of the Bragg fiber with a defect layer can be used as a band-rejection filter,whose characteristics are mainly determined by the structure of the Bragg fiber.The simulation results show that the bandwidth of such a band-rejection filter is dependent on the number of the periodic high/low index layers in both sides of the defect layer in the cladding of the Bragg fiber.     

Theoretical Study on a Cluster-Seven-Core Photonic Crystal Fiber with High Nonlinearity and High-Power Endurance

We present a novel cluster-seven-core photonic crystal fiber which possesses high nonlinearity and supports the high-power pumping. Its nonlinearity coefficient and effective mode area are calculated by the full vector multipole method. Compared with the single core PCF, the cluster-seven-core photonic crystal fiber can support high-power beam transmitting in the core, and simultaneously has high nonlinearity. This kind of photonic crystal fiber can be applied to the photoelectron-device field.     

对电泳液中颜料粒子运动性能的研究

详细介绍了胶体悬浮液作为一种显示用电泳液时的电学性能,分析了电泳颗粒的运动特征;针对目前有些文献中提到的介电泳现象以及利用介电泳现象制成的无源矩阵驱动方式,从理论角度进行了分析。指出介电泳现象在理论上确实存在,但是绝大多数的电泳液在显示时介电泳现象都很微弱,很难实现廉价、大面积的无源矩阵驱动;最后以一种电泳液为例测试了其反射谱,从实验角度验证了此结论, 并给出了最佳的驱动参数。     

Subwavelength-resolution direct writing using submicron-diameter fibers

<正>A novel direct writing technique using submicron-diameter fibers is presented.This technique adopts contact mode in the process of writing,and submicron lines with different widths have been obtained. Experimental results demonstrate that the resolution of this technique can be smaller than the exposure wavelength of 442 nm,and 380-nm-wide line is achieved.In addition,the distribution of light fields in the photoresist layer is analyzed by finite-difference time-domain method.     

聚丙烯纤维加固土融沉特性的离散元数值模拟研究

针对掺入纤维对土体冻融特性的影响进行离散元数值模拟,首先自研了过程感知融化固结系统,基于融沉试验,提出了微观参数折减法模拟融化过程,分析了纤维掺量、纤维长度、土样高度的影响规律。结果表明：离散元方法可对融沉过程进行较为有效的模拟,并可得到最优纤维掺量,对于模拟工况,最优纤维掺量为0.1%;从融化压缩模量看,纤维长度与掺量为敏感影响因素,土样高度为次要因素;掺入纤维对土体强度与融沉特性的提升效果具有一致性。     

碳点/海藻酸复合荧光纤维的制备及应用

以超支化聚乙烯亚胺和柠檬酸为原料,采用水热合成法制备了荧光碳点,探究了碳点的荧光性能和对四环素和Fe³⁺的传感特性。通过PEI表面氨基修饰,在EDC/NHS催化作用下通过羧胺缩合接枝到海藻酸纤维表面,得到了具有蓝色荧光的碳点/海藻酸复合荧光纤维。通过扫描电镜、共聚焦荧光显微镜和万能拉伸仪表征了纤维的微观形貌、荧光特性和机械性能,探究了纤维的荧光稳定性和传感性能。     

微乳液静电纺丝制备多孔Nb4N5纤维及其电化学性能

以五氯化锯为原料,液体石蜡为分相剂,采用微乳液静电纺丝技术制备前驱体纤维,再经氨气还原氮化得到多孔氮化锯纤维.利用XRD、SEM、BET等进行物相及微观结构表征,结果表明合成的纤维为四方Nb4N5晶相,纤维连续,直径为260 nm,由于液体石蜡分相以及助纺剂PVP的分解作用,在纤维上形成较多孔道结构,其BET比表面积为125m2/g,孔径为2～5nm范围内的孔结构比例较高,同时在5～10 nm 范围也存在较多的孔道结构,平均孔径为7.3 nm.采用CV、GCD及EIS等测试其电化学性能发现,氮化锯纤维的储能主要受电极表面电荷传递过程控制的,外表面比电容贡献高,这得益于分布在纤维中的孔结构,其可为离子传输提供通道,并为电化学反应提供空间.当电流密度为5mA/g时,比电容为151 F/g,能量密度为7.73 Wh/kg时,功率密度为3.03 W/kg,其经2000次循环后其比电容保持在95;以上.     

纤维素溶剂研究进展

概述了纤维素溶剂的重要研究进展,主要包括N-甲基吗啉-N-氧化物(NMMO)在85℃以上高温可破坏纤维素分子间氢键,导致溶解;氯化锂/二甲基乙酰胺(LiCl/DMAc)在100℃以上可溶解纤维素;1-丁基-3-甲基咪唑盐酸盐([BMIM]Cl)和1-烯丙基-3-甲基咪唑盐酸盐([AMIM]Cl)离子液体,含强氢键受体Cl-离子,通过它们与纤维素羟基作用而引起溶解.氨基甲酸酯体系则是通过尿素与纤维素在100℃以上反应转变为纤维素氨基甲酸酯,然后再溶解于NaOH水溶液中;氢氧化钠/水体系,只能溶解结晶度和聚合度较低的纤维素;NaOH/尿素、NaOH/硫脲和LiOH/尿素水溶液体系,它们预冷至-5~-12℃后可迅速溶解纤维素.主要是通过低温产生小分子和大分子间新的氢键网络结构,导致纤维素分子内和分子间氢键的破坏而溶解,同时尿素或者硫脲作为包合物客体阻止纤维素分子自聚集使纤维素溶液较稳定.低温溶解技术不仅突破了加热溶解的传统方法,而且可推进化学"绿色化"进程.共引用参考文献50篇.     

Formation of Ultrafine Apatite Fibers by Sol-gel/Electrospinning

Ultrafine apatite fibers were prepared by electrospinning of sol-gel precursor/poly（ vinyl pyrrolidone） （PVP） solutions followed by subsequent calcination. The as-electrospun and calcinated fibers were observed under a scanning electron microscope and an optical polarizing microscope. Results show that the morphology and the diameter of as-electrospun fibers strongly depend on the viscosity and the surface tension of sol-gel precursor/PVP solutions. After calcination, the smooth as-electrospun fibers shrink and the fiber diameter decreases because of the removal of the polymer. The chemical evolution upon the transformation of the precursor from a gel to the final apatite fibers was investigated by thermogravimetric-differenfial thermal analysis, X-ray diffraction, and Fourier transform infrared spectroscopy. It is thus suggested that the crystalline structure of the calcined fibers is largely influenced by the calcination temperature. After being calcined at 600 ℃, the apatite fibers with a diameter of about 280 nm containing β-tricalcium phosphate were obtained.