All-Solid-State Nd:YAG Laser Operating at 1064nm and 1319nm under 885nm Thermally Boosted Pumping

We report a high-effciency Nd：YAG laser operating at 1064 nm and 1319nm, respectively, thermally boosted pumped by an all-solid-state Q-switched Ti：sapphire laser at 885 nm. The maximum outputs of 825.4 m W and 459.4mW, at 1064nm and 1319nm respectively, are obtained in a 8-ram-thick 1.1 at.% Nd：YAG crystal with 2.1 W of incident pump power at 885nm, leading to a high slope efficiency with respect to the absorbed pump power of 68.5% and 42.0%. Comparative results obtained by the traditional pumping at 808nm are presented, showing that the slope efficiency and the threshold with respect to the absorbed pump power at 1064nm under the 885nm pumping are 12.2% higher and 7.3% lower than those of 808rim pumping. At 1319nm, the slope efficiency and the threshold with respect to the absorbed pump power under 885nm pumping are 9.9% higher and 3.5% lower than those of 808 nm pumping. The heat generation operating at 1064 nm and 1319 nm is reduced by 19.8% and 11.1%, respectively.     

Efficient Compound-Cavity Eye-Safe KTP OPO at 1.57 μm Pumped by an Electro-Optic Q-Switched Nd：YAG Laser

An efficient high-energy eye-safe optical parametric oscillator （OPO） based on a type-Ⅱ non-critically phasematched KTP crystal is demonstrated. The KTP OPO is pumped by a quasi-cw diode side-pumped electrooptic Q-switched Nd：YAG laser in a compound-cavity configuration. The maximum output energy of the signal wavelength at 1.57 μm b 66.5 m J, corresponding to an electrical-to-optical conversion efficiency of 4.47% and an optical-to-optical conversion efficiency of 12.1%. The pulse width （FWHM） is about 3.6 ns with a peak power of 18.5 MW. The output energy is insensitive to repetition rate and demonstrates good stability.     

醇改性剂对两种手性农药对映体拆分的影响

对两种手性农药马拉疏磷和粉唑醇进行了对映体的高效液相色谱手性拆分。使用纤维素-三（3,5-二甲基苯基氨基甲酸酯）手性固定相,流动相为正已烷,流动相中添加乙醇、丙醇、异丙醇、丁醇和异丁醇为改性剂,考察了各种醇含量对手性拆分的影响：实验结果显示,该固定相对两种手性农药都具有很好的分离效果。异丙醇、丁醇和异丁醇都适于作马拉疏磷对映体拆分的改性剂,而乙醇和丙醇的效果较差,对于粉唑醇,异丙醇改性剂的效果则相对较好。醇含量对拆分的影响趋势为：醇的含量减少会导致保留增强,分离效果增加。     

尿样及动物组织中甲氧苄氨嘧啶残留量的高效液相色谱-串联质谱测定法

采用微量化样品前处理技术,以固相萃取为净化方法,电喷雾正离子多反应监测方式建立了尿样及动物组织中甲氧苄氨嘧啶残留量的液相色谱-串联质谱联用测定法.检出限为0.1 ng/g,线性范围均大于3个数量级,线性方程的相关系数大于0.999,组织样品和尿样的回收率分别为89%和93%.     

微波诱导Fe2O3/Al2O3催化剂催化氧化处理水中苯酚

 以γ-Al2O3为载体,采用浸渍-焙烧法制备了Fe2O3/Al2O3催化剂,并将其应用于微波诱导催化氧化处理模拟含酚废水. X射线衍射和X射线荧光光谱测试结果表明,活性组分氧化铁在催化剂中以α-Fe2O3的形式存在,其含量为3.71%. 与载体氧化铝相比,Fe2O3/Al2O3催化剂的比表面积和平均孔径及平均孔容略有降低. 对于100 mg/L的模拟含酚废水,最佳的处理工艺条件为: 微波辐照功率400 W,辐照时间5 min,催化剂加入量60 g/L,H2O2浓度600 mg/L,体系pH＞4. 在此工艺条件下,水中苯酚的去除率达97.98%. 催化剂连续使用20次后苯酚去除率仍达96.34%. 表观反应动力学研究表明,在氧化铁催化剂存在的条件下,微波诱导H2O2产生氧化性极强的羟基自由基,整个反应过程可分为微波诱导阶段和催化氧化阶段,两个阶段的氧化过程均符合一级反应动力学规律.     

液相色谱-串联质谱联用法测定蜂蜜及水产品中硝基呋喃类抗生素代谢物残留量

采用微量化样品前处理技术,以邻硝基苯甲醛为衍生剂,电喷雾正离子多反应监测方式建立了蜂蜜及水产品中四种硝基呋喃类抗生素代谢物残留量同时测定的液相色谱-串联质谱联用法。方法的检出限为0.02～0.3 ng/g,线性范围均>10~2,线性方程的相关系数>0.997,回收率为79.0％～95.6％。     

反相高效液相色谱法同时测定化妆品中的9种糖皮质激素

建立了化妆品中9种糖皮质激素的反相高效液相(RP-HPLC)测定方法.采用酸化甲醇振荡提取,HLB固相萃取小柱净化,HPLC分离测定.在定量范围内均呈良好的线性关系(r≥0.999);回收率为85.0%～99.5%,相对标准偏差小于5.8%,检出限(LOD) (S/N≥3)为1.0 ng,定量限(LOQ) (S/N≥10)为2.0 ng.该法可用于化妆品中泼尼松龙、氢化可的松、可的松、甲基强的松龙、地塞米松、氟米松、倍氯米松、曲安奈德和氟轻松的检测.     

PPLN晶体差频测量飞秒激光脉冲的载波包络相移

在飞秒激光频率梳系统中，通常采用自参考技术测量飞秒激光脉冲的载波包络相移，但该技术需要采用光子晶体光纤进行光谱扩展从而增加了系统的不稳定性，这种技术已经制约了高稳定度的飞秒激光频率梳的发展.采用PPLN晶体差频法测量了宽谱钛宝石振荡器输出的7fs激光脉冲的载波包络频移，得到了大于30dB的拍频信号，为研制无光纤的新一代高稳定度光学频率梳奠定了基础.     

一种基于加速度计和天文的卫星自主导航新方法

直接敏感地平是一种典型自主天文导航方法,该方法简单可靠,易于实现,但是由于常用卫星轨道动力学J2模型精度有限,地球敏感器精度较低,因此导航精度不高。加速度计是测量运载体线加速度的常用惯性导航设备,当航天器在轨运行时,星载加速度计能够测量航天器所受发散力。结合上述两种方法的特点,提出一种将加速度计和天文相结合的自主天文导航新方法。在常用卫星轨道动力学模型基础上,引入大气阻力和太阳光压系数模型作为自主导航系统状态方程的一部分,并建立近地空间环境下星载加速度计的测量模型,将其与直接敏感地平均作为导航系统观测方程。设计基于信息融合的自主导航滤波方法,通过对多种导航模式进行数值仿真及结果分析,结果表明所设计方法提高了系统定位精度62.8%和速度精度63.9%,增强了系统可靠性。     

Electronic structure of PCBM

We have studied the electronic structure of [6,6]-phenyl-C₆₁-butyric-acid-methyl-ester (PCBM) using synchrotron radiation photoelectron spectroscopy (PES) measurements and first-principles calculations. The PES spectrum of the entire occupied valence band is reported, which exhibits abundant spectral features from the Fermi level to ～24 eV binding energy. All the spectral features are broadened as compared with the cases of C₆₀. The reasons for the broadening are analysed by comparing the experimental data with the calculated energy levels and density of states. Special attention is paid to the analysis of the C₆₀ highest occupied molecular orbital (HOMO)-1 derived states, which can play a crucial role in the bonding at the interfaces of PCBM/polymer blenders or PCBM/electrodes. Besides the well-known energy level splitting of the C₆₀ backbone caused by the lowered symmetry, C 2p states from the side chain mix or hybridize with the molecular orbitals of parent C₆₀. The contribution of the O 2p states can substantially modify the PES spectrum.