148 research outputs found
The Response Rate of The SERS Intensity When A Potential Step is Applied
SErS谱峰强度对电位阶跃的响应速率顾仁敖,吴芸,乔专虹,姚建林(苏州大学化学系苏州215006)田中群,李五湖(厦门大学化学系厦门361005)THErESPOnSErATEOfTHESErSInTEnSITyWHEnAPOTEnTIAlSTEPI...Abstract Time-resolved surFace-enhanced Raman spectroscopy(TRSERS)has been combined with the potential step method to study thiourea and ClO coadsorbed at Ag electrodes.When a potential is applied, the response rate of the SERS intensity depends on the potential being stepped the stepping direc-tion, the concentration of TU and the diFFerent SERS band
The Dependence of The SERS Intensities Rate on The Potential
SErS谱峰强度比与电位的关系顾仁敖,吴芸,乔专虹,姚建林(苏州大学化学系215006)田中群,李五湖(厦门大学化学系361005)THEdEPEndEnCEOfTHESErSInTEnSITIESrATEOnTHEPOTEnTIAl¥gurEnAO...Abstract Time-resolved surFace-enhanced Raman spectroscopy ( TRSERS)has been combined with the potental step inethod to study thiourea and ClO coadsorbed at Ag electrodes.When the potential changed, iF the ratio of two SERS bands intensities were stable, the two bands must have some common properties.The two bands at 932cm--(-1) and 1094cm--(-1) have similar properties
Raman and AFM Characterization of Au and Cu Nanorod and Nanowire Arrays
通过电化学氧化法制备具有不同孔径氧化铝模板 ,利用交流电镀的方法在模板中沉积金属 ,再用酸溶解模板可以得到相应尺度的金属纳米线或纳米棒的阵列 .本文利用原子力显微镜和表面增强拉曼技术分别表征了金和铜两种金属纳米线阵列 .研究结果表明 ,作为探针分子的硫氰(SCN )在金属纳米线上的碳氮三键的振动频率随纳米线直径的增大而蓝移 .这一现象可能是因为尺寸效应对纳米线的费米能级造成影响 ,使不同直径的金属纳米线电子结构存在微小的差别 .Recently metal nanowires (nanorods) have aroused tremendous interest because of their novel properties and potential applications in wide fields [1] . Many two?dimensional nanowire arrays of semiconductors and metals with different diameter and length have been made by using template synthesis method. To characterize the novel optical, electronic and magnetic properties of these materials, UV?Vis and fluorescence spectroscopies are two of the most wildly used methods [2, 3] . Raman spectroscopy has, however, only been applied to the characterizing of semiconductor nanowires and carbon nanotubes [4,5] . Important and meaningful information can be obtained in these cases, as some forbidden Raman modes in the bulk materials become Raman active [4, 5] . Raman spectroscopy is apparently not suitable to study metal nanowires since it can only detect the mechanical vibration bands located in the extremely low frequency region. Consequently, an alternative way has to be established to study the metal nano?wires (?rods) with Raman spectroscopy. In the present work, we have taken the probe molecule strategy and used surface?enhanced Raman spectroscopy (SERS) to characterize metal nanorods (nanowires). It is well known that for a molecule which interacts strongly with a surface, its vibrational band frequency and shape are very sensitive to the electronic property, the chemical environment and the morphology of the surface. Hence Raman spectroscopy has long been used to analyze the atomic structures and the electronic properties of the surface indirectly through assessing carefully the spectral changes of the adsorbate known as a probe molecule. On that account, it is of great interest to diagnose the electronic structures of the metal nanorods with the vibrational spectrum of a probe molecule. We have examined the changes in the electronic properties of the nanorods through analyzing the spectral changes of the probe molecule. For this purpose a typical SERS molecule of SCN - was employed. The nanorod arrays of Au and Cu with different diameter from about 15 nm to 130 nm were fabricated electrochemically by means of the anodic aluminum oxide (AAO) templates. To partially expose metal nanowires with various lengths, the AAO template was chemically etched off to a certain extent by an aqueous solution of phosphoric acid or sodium hydroxide as shown in Fig. 1. After the template was etched off, the nanowires can be characterized by TEM, see Fig. 2. The tapping mode AFM image was obtained on a scanning probe microscope (Nanoscope IIIa). SERS measurements were performed on a confocal microprobe Raman system (LabRam I).作者联系地址:厦门大学固体表面物理化学国家重点实验室!化学系福建厦门361005,厦门大学固体表面物理化学国家重点实验室!化学系福建厦门361005,南京师范大学化学系!江苏南京,210097,厦门大学固体表面物理化学国家重点实验室!化学系福建厦门361005,厦门大学固体表面物理化学国家重点实验室!Author's Address: State Key Lab.for Phys.Chem.of Solid Surf.,Xiamen Univ.,Xiamen 361005, China; 1 Dept. of Chem., Nanjing Norm
浅层流态化
随着流化床结构及局部性能研究的深入,流化床已不再被看作浑然一体了。研究发现,分布板附近的区域(分布板区)以及浓相床层以上的区域(稀相区)与床层主体(鼓泡区)有许多不同。特别是分布板区越来越受到研究者的重视。这不仅因为分布板是影响流化床均匀性和稳定性的重要构件,又是气泡的发源地,它的结构决定了气泡的
铁鳞流态化氢还原的数学模拟——固相加工鼓泡床模型
本文基于气泡理论,提出了 B 类物料固相加工的流化床模型。结合已经获得的粗粒铁鳞氢还原的反应速度方程,对φ0.6米的中试装置进行了数学模拟,计算预测和实验结果相当一致。本文还采用了一些简单流化床模型对两套热试装置进行了计算预测。结果表明,对于较小的反应器,几个模型的预测结果比较接近,且与实测结果比较吻合;随着反应器尺寸的扩大,一些简单模型的计算结果偏离实验值,而本文所提模型能够适应反应器的放大
彩色石英砂生产新工艺的研究
本文系统地介绍了彩色石英砂生产新工艺的研究过程。结果表明,采用新型稀相辐射加热反应炉和独特着色剂配方的新工艺。具有流程简单,设备投资少;加热速度快,能耗低,可连续生产;产品质量好,成本低等特点,较好地解决了旧工艺存在的一系列问题
煤炭拔头提取液体燃料新工艺
随着经济的发展,国内对优质液体燃料的需求日趋增加,预计今后供需矛盾将更为突出。中国能源资源的特点是油少煤多,若对较年轻的煤种采用快速热解和快速冷凝的拔头工艺,并与循环流化床锅炉相结合,可望获得较高的油品收率,同时实现煤的洁净燃烧。而研究和开发一种新型的热解反应器是实现新工艺工业化的关键课题
秸秆分层多级转化液体燃料新工艺的研究进展
目前,秸秆主要作为性质单一组分的纤维素原料而采用生物转化法或快速热解法加以利用。生物转化法主要利用纤维素,而利用木质素和半纤维素较困难;快速热解生物质又使部分组分低值利用,而且得到的生物油品质低。为解决单一的生物或热转化方式存在的问题,提出秸秆分层多级转化液体燃料的新构思,即以秸秆“组分分离、分级定向转化”为核心,将生物转化和热转化有机结合多级转化生产燃料酒精与生物油。研究结果表明,秸秆经过汽爆处理后,采用高浓度发酵 分离乙醇耦合系统,可降低纤维素酶用量,提高了纤维素酶解效率,而且简化操作过程,使蒸馏前乙醇浓度达到6 0 %以上。发酵乙醇剩余物再经热解后,不但热解温度较原秸秆明显降低,而且所得生物油品质有了明显改观
液—固脉动床基本流体力学特性的研究
本文在内径为φ47mm 的有机玻璃床中,进行了有净流动的液—固脉动床流动性实验。研究了频率为1~5Hz,振幅为0.27~1.0cm,正弦脉动对液—固脉动床基本流体力学特性的影响。实验结果表明:引入脉动之后,同经典流化床相比,最小流化速度减小,最小流化压降降低,固定床段的压降发生了非常复杂的变化。实验中定义了一个完全流化速度,用于描述床层引入脉动之后的流化状态。实验还发现在液—固床中也存在共振现象。并利用简单的活塞模型进行了计算
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