光纤加速度传感器研究进展

光纤加速度传感器与传统加速度传感器相比，不但能抗电磁干扰，而且体小、质轻、动态范围宽、精度高、能在恶劣环境下工作，因此受到各先进国家军事与商业领域的极大重视，各种实用的光纤加速度传感器不断涌现。主要有光强调制型和相位调制型两大类。光强调制式有反射式、透射式和偏振式等等。相位调制式有Ｍａｃｈ－Ｚｅｎｄｅｒ干涉仪、Ｍｉｃｈｅｌｓｏｎ干涉仪和Ｆａｂｒｙ－Ｐｅｒｏｔ干涉仪。有一维的，也有二维的；有与水听器组合在一起的，也有与光纤陀螺仪组合的光纤加速度传感器。最小的已经做到２．５ｃｍ长，直径仅０．２５ｍｍ；测量精度已能达到１μｇ；共振频率可达到１０ｋＨｚ。为了克服温度不稳定性对测量精度的影响，人们采用了３×３耦合器解调法，双光路法，由单臂式改成推挽式等。一旦关键技术得以克服，光纤加速度传感器将会在惯性导航和其它领域发挥更重要的作用。本文将分别介绍目前各种类型光纤加速度传感器的结构、特点、走向实用化存在的问题。     

用超磁致伸缩调谐光纤光栅的光分/插复用器

提出并研究了一种新型多信道切换的全光分/插复用器,它主要由光纤Bragg光栅(FBG)和一对光环行器组成.采用了一种高效的超磁致伸缩材料(GMM)使FBG产生有效的Bragg波长偏移.用控制电流来调控FBG的应变和Bragg波长偏移.用4只相同的FBG与波长叠加技术相结合,可建立能提供15种不同下路信道方式的OADM.     

Fiber Optical Bragg Grating Refractometer

We have demonstrated an evanescent field refractive indexfiber sensor comprising a 42-mm Bragg grating in an etched fiber together with a tunable Distributed Bragg Reflector (DBR) laser. Characterization of different aqueous sucrose solutions resulted in a resolution of roughly 10 mM sucrose. The sensor in the presented form has a theoretical sensitivity of higher than 10 5 refractive index unit (riu) in a refractive index region close to the cladding index of the fiber. However, the technique allows for an even higher sensitivity than 10 6 riu with a proper signal processing scheme.     

Chemical Reactions in the Manufacture of Waveguides for Long Distance Optical Data Transmission

One of the modern high technologies which has advanced enormously in the last few years is glass fiber technology. This is used in the manufacture of glass fibers for lighting purposes and for the optical transfer of analog and digital data with a high transfer density. The technical demands made on the glass fibers required for data transfer, the optical waveguides, are extremely high and are already fulfilled to a large extent by industry. At present about four million kilometers of fiber, worth ca. 800 million DM are produced worldwide (10% in the Federal Republic of Germany). Numerous chemical processes take place during the manufacture of optical waveguides. However, in contrast both to the high and constantly growing demands on the quality and to the increasing production volume of such fibers, little is in fact known about the reactions involved. The present article will attempt to develop a picture of the multifarious reactions occurring in the course of this technical process on the basis of literature data and our own studies.     

Novel fiber-optic biosensor based on immobilized glutathione S-transferase and sol–gel entrapped bromcresol green for the determination of atrazine

The aim of this work was to investigate, for the first time, the potential of the enzyme glutathione S-transferase I (isoenzyme GST-I) for uses in analytical chemistry. A novel fiber-optic biosensor for the detection and determination of the triazine herbicide atrazine was developed based on maize GST-I expressed in E. coli. The sensing bioactive material was a three-layer mini-sandwich. The enzyme was immobilized on the outer layer that consisted of a hydrophilic polyvinylidenefluoride membrane. This membrane was supported on an inner glass disk by means of an intermediate binder sol–gel layer that incorporated bromcresol green (BCG). The biosensor operated in a static mode at 25 °C and the rate of the enzymatic reaction, using atrazine as a substrate, served as an analytical signal. A calibration curve was obtained for atrazine, with analytically useful concentration range 2.52–125 μM. The sensor detection limit was 0.84 μM. The reproducibility of atrazine sensing was in the order of ±3–5%. The method was successfully applied to the determination of this herbicide in real water samples, without sample preparation steps. Atrazine recovery ranged between 85 and 110%. No interference from other pesticides, such as alachlor and carbaryl was observed in the absence of atrazine. The immobilized enzyme retained about 75% of its original activity after 1 month use. Simply unscrewing the terminal holding ring of the probe and placing a new bioactive sandwich could easily replace a deteriorated mini-sandwich.     

醋酸十二铵的吸附和SiO2悬浮液的稳定性

（1）测定了醋酸十二烷基铵（DAA）在CAB－O－SIL上的吸附，其等温线属双平台或LS型[1－3，5]；（2）NaCl的存在使DAA的吸附增加．但不影响其低浓度下第一平台的吸附量；HCl的存在则在全浓度范围内抑制了DAA的吸附，（3）测定了CAB－O－SIL颗粒在上述各溶液中的悬浮液的稳定性；（4）根据表面形成小胶团的吸附理论（即二步模型产）[2，3，5，]，并借助电导跟踪溶液中发生的变化，满意地解释了吸附和聚沉的实验结果．     

交联聚乙烯基吡咯烷酮的合成及其性能研究

以乙烯基吡咯烷酮（NVP）为单体，二乙烯基苯为交联剂，AIBN为引发剂，采用悬浮聚合法合成了性能稳定的交联聚乙烯基吡咯烷酮（PVPP），研究了聚合温度，引发剂用量，交联剂用量和反应气氛等因素对产率，溶胀性能和吸附性能的影响，并用红外光谱和扫描电镜等对产物的结构、性能和表面形貌进行了表征。     

Synthesis and characterization of hybrid borosiloxane gels as precursors for Si–B–O–C fibers

The sol–gel method has been used for the synthesis of borosilicate gels from mixtures of methyltriethoxysilane (MTES) and dimethyldiethoxysilane (DMDES) and boric acid. The use of boric acid, B(OH)₃ allows the hydrolysis and condensation of hybrid silicon alkoxides without further addition of water or catalyst. The use of difunctional silicon units, –(CH₃)₂SiO– promote the formation, during the sol–gel process, of linear oligomers which facilitate fiber drawing before gelation. Gel characterization performed by FT-IR, XRD, TG-DTA and DCS analysis indicates the formation of a mixed network with incorporation of the boron units via =B-O-Si≡ bridges. The formation of borosiloxane bonds seems favored by the presence of DMDES. SiBOC glasses were obtained after pyrolysis of the borosilicate gels in argon atmosphere at 1000 °C. TG-DTA study indicates that the ceramic yield decreases by increasing the amount of DMDES. Gel fibers were successfully prepared from convenient partially-aged solutions by hand drawing. Pyrolysis of the obtained gel fibers under argon atmosphere at 1000 °C open the possibility to produce SiBOC homogeneous glass fibers with diameter as low as 10 μm.     

由聚苯胺粒子组成的电流变液的研究

由经碱处理的掺杂态聚苯胺（ＰＡｎ）制得高介电常数的半导体ＰＡｎ粒子，将其悬浮于电绝缘油可组成电流变液，讨论了电流变（ＥＲ）液的静态屈服应力（τ＿ｓ），电流密度等性能与ＰＡｎ的介电常数（ε＿ｐ），导电率（σ），体积分数和应用电场强度的关系。对导电率相同的ＰＡｎ粒子，用氨水处理的ＰＡｎ粒子ε＿ｐ较用ＮａＯＨ液处理的高，前者在σ足够低如σ≤１．０×１０￣（－７）／ｃｍ时，ＥＲ液的τ＿ｓ随偶极系数的平方（β￣２）的增大而呈现非线性增加；后者ＥＲ液的τ＿ｓ随β￣２的增大出现一最大值．结果表明：由聚苯胺粒子可组成高电流变活性的无水ＥＲ液．     

Crystallization behavior and biodegradation of poly(3-hydroxybutyrate) and poly(ethylene glycol) multiblock copolymers

Block copolymerization by using isocyanates is an effective method for incorporating PHB and PEG because it can prepare copolymers with good properties, such as toughness, strength, and so on. In this study, we adopted soil suspension system to estimate the biodegradability of a series of PHB/PEG multiblock copolymers with different compositions and block lengths. In the degradation process, the changes in weight loss, molecular weight, and tensile strength were periodically measured to determine the biodegradability, and the surface morphology was also observed by SEM. In contrast to pure PHB, the weight loss of the copolymer was relatively lower. On the other hand, the tensile strength and molecular weight experienced apparent decrease, and for BHG1000-3-1, they reached 46.7% and 77.7% of the initial value, respectively. SEM observation showed that the surface was covered with numerous erosion pits. All these indicate that the degradation indeed took place and long-chain molecules have been hydrolyzed into shorter ones. The crystallization behavior was also investigated by DSC and WAXD. The results showed that both the segments, PEG and PHB, can form crystalline phases at lower PHB contents ranging from 29% to 44%, and when PHB component was more than 60%, only PHB phase can crystallize.