激光尘埃粒子计数器微型光学传感器的研究

研制成功便携式激光尘埃粒子计数器的核心部件——微型光学传感器。该传感器采用直角散射光收集形式。以高功率半导体激光器作为光源，同时采用高性能的PIN型光电二极管作为光电探测器。散射光收集系统为单一大数值孔径的球面反射镜，其对粒子散射光的收集角范围从20°到160°。粒子散射光信号是脉冲信号，其频谱成份主要在高频段，所以在PIN型光电二极管后用一个带通式前置放大器来消除外界的低频噪声．根据米氏散射理论计算了该光学传感器的光散射响应特性，并用聚苯乙烯标准粒子实测了该光学传感器的性能。结果表明，该系统具有高的信噪

Direct detection of Yersinia pestis from the infected animal specimens by a fiber optic biosensor

The FOB-3, anew type fiber optic biosensor, is designed to rapidly detect a variety of biological agents or analytes with better stability, sensitivity and specificity. In order to detect Y. Pestis, a sandwich immunoassay was developed by using the purified antibody against antigen FI immobilized on polystyrene probes as the capture antibody and the monoclonal antibody-Cy5 conjugate as the detector. After a series of optimization for the stability, sensitivity and specificity of the FOB-3, 50-1000 ng/ml of antigen FI and 6 x 10(1)-6 x 10(7) CFU/ml Y. pestis could be detected constantly in about 20 min, and Y pestis could be detected specifically from Y. pseudotuberculosis, Y. enterocolitica, B. anthracis and E. coli. Then, 39 blind samples, including 27 tissues of mice infected with Y pestis and 12 tissues of healthy mice as negative control, were detected with the FOB-3. 92.6% infected tissues were identified from the tissues of healthy mice and the tissues containing more than 100 CFU/ml bacteria could be detected by the biosensor. The results demonstrated the feasibility of the FOB-3 as an effective method to detect Y. pestis rapidly and directly from the infected animal specimens with the advantage of portability, simple-operation as well as high sensitivity and specificity. (c) 2006 Elsevier B.V. All rights reserved.

Ultrahigh-resolution fiber-optic image guides derived from microstructured polymer optical fiber preforms

Ultrahigh-resolution fiber-optic image guides-fused image fiber, faceplate, and taper-were fabricated by using microstructured polymer optical fiber (MPOF) preforms composed of two polymers: polymethylmethacrylate and polystyrene. The pixel diameter in the resultant MPOF-based image guides was as small as 3 mu m. The imaging capabilities of these types of fiber-optic elements were demonstrated. (C) 2009 Optical Society of America

Preparation and optical property of a novel hydrophobic anti-reflection coating for KDP crystal

A novel inorganic-organic hybrid hydrophobic anti-reflection silica film used for laser crystal was obtained by sol-gel process. The film consisted of silica sols mixed with a small amount of polymethyl methacrylate (PMMA) or polystyrene (PS). The optical transparency, hydrophobic property and surface morphology of the film were characterized by UV-VIS-NIR spectrophotometer; contact angle instrument and Scanning Electron Microscopy (SEM), respectively. The results showed that the anti-reflection coating had good hydrophobility and optical transparency from 400 nm to 1200 nm. The contact angle reached to 130-140 degrees. SEM images indicated the hydrophobic films modified with PMMA or PS had compact structure compared to the pure silica sol film. (C) 2008 Elsevier B.V. All rights reserved.

聚苯乙烯薄膜溶胀/沉淀过程中的微观结构演化

本论文以聚苯乙烯薄膜为研究对象,研究应用溶剂/非溶剂连续处理而改变聚苯乙烯薄膜结构的方法。首先采用旋转涂膜法制备聚苯乙烯薄膜，利用谱学椭圆偏振仪、同步辐射掠入射超小角X射线散射与X射线反射方法来联合测定薄膜性质，进行了以下实验： 一． 离线实验：聚苯乙烯的四氢呋喃溶液在经亲水性预处理的硅片基底上旋转涂膜，退火后，聚苯乙烯薄膜连续浸入其溶剂N,N-二甲基甲酰胺与非溶剂乙醇，经过溶胀和沉淀过程，彻底改变了原来薄膜的表面结构，原子力显微镜和掠入射小角X射线散射在薄膜表面实验结果清晰显示，薄膜表面形成了不同尺度的聚苯乙烯聚集体，。结果表明同步辐射掠入射小角X射线散射是一种新颖，简单易行的观察薄膜表面结构的强有力的手段。溶剂/非溶剂处理聚苯乙烯表面的方法简便易行，是一种非常有潜力的改善聚苯乙烯表面结构的方法。 二． 在线实验：根据离线实验结果，自行设计制造了一个椭圆偏振仪样品池，用椭圆偏振仪上在线跟踪气态溶剂/非溶剂处理聚苯乙烯薄膜，努力追踪溶剂/非溶剂处理聚苯乙烯薄膜过程中，薄膜结构的动态变化规律。结果显示，气态溶剂/非溶剂处理薄膜表面的结果与用液态溶剂/非溶剂处理的结果不同，处理后的薄膜表面性质没有明显改变，而且加入非溶剂后椭偏参数随时间的一级指数衰减与膜厚成线性关系。原因可能是样品池内为混合气体，非溶剂蒸汽压不够，不足以引起聚苯乙烯分子链的沉淀，溶胀的薄膜又回复原态。

聚苯乙烯-聚丁二烯嵌段共聚物反转相行为的研究

本论文以聚苯乙烯（PS）一聚丁二烯（PB）三嵌段和二嵌段共聚物体系为研究对象，利用聚合物的软有序化，控制聚合物分子链的取向和聚集条件，系统地考察了嵌段共聚物在由溶液成膜的过程中动力学效应和墒效应对其相结构和相转变行为的影响。并探讨了不同相结构和其力学性能之间的构效关系。设计了聚苯乙烯（PS）一聚丁二烯（PB）（PS≈30wt％）／非选择性溶剂体系，通过改变溶剂的挥发速率，控制了嵌段共聚物薄膜相结构形成的动力学过程。在快速挥发的条件下，在嵌段共聚物中观察到了特殊的反转相结构，即共聚物中含量多的组分（PB）形成了分散相，而当溶剂挥发很慢的条件下，得到的是热力学较稳定的正常相的结构。对不同分子量的一系列嵌段共聚物的研究表明，反转相的形成和分子量相关，与聚合物的链段数目无关，只有在低于临界分子量 （Mw=70-100 KDa）的嵌段共聚物中，成膜过程的动力学过程才影响嵌段共聚物薄膜的最终相态，即形成反转相。这种依赖于分子量的相转变行为，揭示了分子链运动速度与环境变化速率的匹配对嵌段共聚物薄膜有序相结构形成的重要作用，即动力学效应对聚合物软有序化的重要作用。利用冷冻干燥的方法，进一步研究了嵌段共聚物在极慢的溶剂挥发下，由溶液膜变成固体膜的过程中，随着溶液浓度的增加，不同聚合物分子链在溶液中自组织形成有序结构的过程。结果表明反转相是由稀溶液向亚浓溶液转变的过程中形成的。通过选取具有代表性的不同亲和性的溶剂：苯和环己烷及其混合溶剂，研究了溶剂对不同链段亲和性的差异对反转相形成的影响。由聚合物一溶剂相互作用参数判断，苯是体系的良溶剂，环己烷是体系的。溶剂，而苯对PS链段有较好的亲和性，与之相反环己烷对PB链段有较好的亲和性，通过对聚苯乙烯（PS）一聚丁二烯印B）二嵌段共聚物在苯和环己烷极其混合溶剂中的相转变行为的研究发现，随着溶剂对含量少的PS链段亲和性的降低，反转相不再出现。这是由于苯与PS．链段、环己烷与PB链段有更好的亲和性，嵌段共聚物在稀溶液中，在耗尽吸引的（depletion attraction）作用下，与溶剂亲和性弱的链段，在溶液中优先发生聚集，而有序聚集后导致的混合熵的损失会被更多的因有序聚集后小分子自由体积增加引起的平移嫡的增量所补偿，因此导致了嫡驱动的软有序化。最后，通过原子力显微镜纳米压印法，分别对反转相和正常相结构的纳米力学性能进行了对比研究，讨论了不同相结构间模量的差异，结果表明软段（PB）形成分散相结构时薄膜的模量总是小于硬段（PS）形成分散相结构时薄膜的模量，这主要是由嵌段共聚物不同组分的相对含量及形成的相的结构决定的。

Behavior of Pentacene Initial Nucleation on Various Dielectrics and Its Effect on Carrier Transport in Organic Field-Effect Transistor

The influence of dielectric surface energy on the initial nucleation and the growth of pentacene films as well as the electrical properties of the pentacene-based field-effect transistors are investigated. We have examined a range of organic and inorganic dielectrics with different surface energies, such as polycarbonate/SiO2, polystyrene/SiO2, and PMMA/SiO2 bi-layered dielectrics and also the bare SiO2 dielectric. Atomic force microscopy measurements of sub-monolayer and thick pentacene films indicated that the growth of pentacene film was in Stranski-Kranstanow growth mode on all the dielectrics. However, the initial nucleation density and the size of the first-layered pentacene islands deposited on different dielectrics are drastically influenced by the dielectric surface energy. With the increasing of the surface energy, the nucleation density increased and thus the average size of pentacene islands for the first mono-layer deposition decreased. The performance of fabricated pentacene-based thin film transistors was found to be highly related to nucleation density and the island size of deposited Pentacene film, and it had no relationship to the final particle size of the thick pentacene film. The field effect mobility of the thin film transistor could be achieved as high as 1.38 cm(2)/Vs with on/off ratio over 3 x 10(7) on the PS/SiO2 where the lowest surface energy existed among all the dielectrics. For comparison, the values of mobility and on/off ratio were 0.42 cm(2)/Vs and 1 x 10(6) for thin film transistor deposited directly on bare SiO2 having the highest surface energy.

Total-internal-reflection fluorescence microscopy with W-shaped axicon mirrors

A scheme based on a W-shaped axicon mirror device for total-internal-reflection fluorescence microscopy (TIRFM) is presented. This approach combines the advantages of higher efficiency compared with traditional TIRFM, adjustable illumination area, and simple switching between wide-field and TIRF imaging modes. TIRF images obtained with this approach are free of shadow artifacts and of interference fringes. Example micrographs of fluorescently labeled polystyrene beads, of Convallaria majalis tissue, and of Propidium-iodide-labeled Chinese hamster ovary cells are shown, and the capabilities of the scheme are discussed. (C) 2010 Optical Society of America

Wettability designing by ZnO periodical surface textures

A facile and effective aqueous chemical synthesis approach towards well control of periodical ZnO textures in large-scale areas is reported, by which considerable adjusting of surface wettability can be realized. With the assistance of polystyrene spheres monolayer template and morphology control agent, we succeeded in preparing a series of ordered ZnO microbowls with different sag height. It was found that the contact angle could be well adjusted by changing geometry of microbowl. Such novel, ordered arrays are expected to exploit the great potentiality in waterproof or self-cleaning micro/nanodevices, and even microfluidic devices. (C) 2010 Elsevier Inc. All rights reserved.

Fracture of colloidal single-crystal films fabricated by controlled vertical drying deposition

Controlled vertical drying deposition method was used to make high-quality single crystal close-packed colloidal films formed of different radii polystyrene latex spheres on glass substrates coming from a low concentration water suspension (0.1% volume fraction). Regardless of the spheres radii the film thickness was about 6.3 microns. However, cracks destroyed the crystalline film structure during the colloidal film growth. The effect of particle radius (85-215 nm range) on film cracking was systematically studied using in situ optical fracture monitoring. Primary parallel cracks run along the vertical growth direction, later followed by secondary branched cracks in-between the primary cracks due to residual water evaporation. Quantitative theoretical relationship between the cracks spacing and particles radius was derived and shows good agreement with experimental observations. Normalized cracks spacing is related to a reciprocal ratio of the dimensionless particle radius.

Applications of Heavy Ion Irradiation in Photonic Crystal Research

Photonic crystals (PC) have received extensive attention for the photonic band gap (PBG). The polystyrene (PS) particles bottom-up approach is a productive method for photonic crystal manufacture, this kind of photonic crystals having an unique PBG that depends on the particle's shape, sizes and defects. Heavy ion irradiation is a very useful method to induce defects in PC and change the shapes of the particles to tune the PBG. MeV heavy ion irradiation leads to an anisotropic deformation of the particles from spherical to ellipsoidal, the aspect ratio of which can be precisely controlled by using the ion energy and flux. Sub-micrometer PS particles were deposited on a Cu substrate and were irradiated at 230 K by using heavy ion energy and fluence in the range from 2 to 10 MeV and 1 x 10(14) cm(-2) to 1 x 10(15) cm(-2); respectively.

流体力学半径对估算胶体微球聚集速率常数的影响

胶体粒子聚集速率常数实验值远低于理论值一直是被普遍关注的问题.聚集速率常数的理论推导是基于粒子的几何半径来考虑的,但决定粒子扩散速率及聚集速率的应该是粒子的流体力学半径(大于几何半径),因而它是使聚集速率常数实验值低于理论值的因素之一.影响流体力学半径的因素很多,其中,带电粒子在溶液中因表面存在双电层,会明显增大流体力学半径,造成聚集速率减慢.而双电层的厚度又随溶液中离子强度的不同而改变.本工作在聚集速率的公式中引入了修正因子,即几何半径与其流体力学半径之比,以修正由于用几何半径代替流体力学半径带来的误差.其中几何半径和流体力学半径可以分别用扫描电镜(SEM)和动态光散射(DLS)来测定.以两种粒径的聚苯乙烯带电微球为例,考察了在不同离子强度下,该误差的大小.结果发现,对于半径为30 nm的微球,用流体力学半径计算的慢聚集速率常数比理论值偏低约8%.该误差随离子强度增加而减少.对于快聚集情况,流体力学半径对聚集速率基本没有影响.

Applications of Heavy Ion Irradiation in Photonic Crystal Research

Photonic crystals (PC) have received extensive attention for the photonic band gap (PBG). The polystyrene (PS) particles bottom-up approach is a productive method for photonic crystal manufacture, this kind of photonic crystals having an unique PBG that depends on the particle's shape, sizes and defects. Heavy ion irradiation is a very useful method to induce defects in PC and change the shapes of the particles to tune the PBG. MeV heavy ion irradiation leads to an anisotropic deformation of the particles from spherical to ellipsoidal, the aspect ratio of which can be precisely controlled by using the ion energy and flux. Sub-micrometer PS particles were deposited on a Cu substrate and were irradiated at 230 K by using heavy ion energy and fluence in the range from 2 to 10 MeV and 1 x 10(14) cm(-2) to 1 x 10(15) cm(-2); respectively.

快重离子在聚苯乙烯中的辐照效应研究

本工作用兰州重离子加速器提供的2.1GeV的Kr离子分别在空气和真空条件下辐照了多层堆叠的聚苯乙烯薄膜样品，辐照剂量在5 * 10~(10)到3 * 10~(12)ions/cm~2之间，辐照温度在室温附近。辐照后对样品分别进行了傅立叶变换红外光谱和紫外可见光谱的测量，由此研究了快重离子辐照聚苯乙烯产生的物理和化学改性。实验结果表明，聚苯乙烯经Kr离子辐照后发生了降解，包括苯环在内的大部分官能团遭到破坏，相应特征峰的吸光度随辐照剂量和能损的增加而减小。与此同时，辐照还在1650-1750cm~(-1)之间和3300cm~(-1)处产生了新的吸收峰，其分别对应于C=O双键的分子振动和C≡C-H的C-H伸缩振动，表明辐照在聚苯乙烯中产生了炔基。实验发现产生炔基需要离子有足够高的电子能损值，在聚苯乙烯中该能损阈值约为1.0keV/nm。在材料经辐照发生降解的同时，样品的光吸收边界逐渐红移，并伴有透光率的下降。详细的测量显示，在紫外可见区材料吸光度的增加随剂量近似呈线性关系，随能损呈约二次方的指数关系。通过对2.1GeV的Kr离子和1.4GeV的Ar离子辐照结果的比较还发现，快重离子辐照产生的物理化学改性不仅与离子的能损有关，还与离子的速度有关。在同一能损条件下，速度越小，产生的效应就越大。文中用径向能量沉积密度和有效化学反应半径对上述结果进行分析讨论。

A strategy for synthesis of ion-bonded amphiphilic miktoarm star copolymers via supramolecular macro-RAFT agent

Amphiphilic supramolecular miktoarm star copolymers linked by ionic bonds with controlled molecular weight and low polydispersity have been successfully synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization using an ion-bonded macromolecular RAFT agent (macro-RAFT agent). Firstly, a new tetrafunctional initiator, dimethyl 4,6-bis(bromomethyl)-isophthalate, was synthesized and used as an initiator for atom transfer radical polymerization (ATRP) of styrene to form polystyrene (PSt) containing two ester groups at the middle of polymer chain. Then, the ester groups were converted into tertiary amino groups and the ion-bonded supramolecular macro-RAFT agent was obtained through the interaction between the tertiary amino group and 2-dodecylsulfanylthiocarbonylsulfanyl-2-methyl propionic acid (DMP). Finally, ion-bonded amphiphilic miktoarm star copolymer, (PSt)(2)-poly(N-isopropyl-acrylamide)(2), was prepared by RAFT polymerization of N-isopropylacrylamide (NIPAM) in the presence of the supramolecular macro-RAFT agent. The polymerization kinetics was investigated and the molecular weight and the architecture of the resulting star polymers were characterized by means of H-1-NMR, FTIR, and GPC techniques. (c) 2008 Wiley Periodicals, Inc.