A Mid-IR 14.1W ZnGeP2 Optical Parametric Oscillator Pumped by a Tm,Ho:GdVO4 Laser

We report a high power and high efficiency double resonant ZnGeP2 （ZGP） optical parametric oscillator （OPO） pumped by a Tm,Ho：GdVO4 laser. We employ a Tm,Ho：GdVO4 laser as the pump source operated at 2.049 μm with M^2 = 1.1. The ZGP OPO can generate a total combined output power of 14.1 W at 3.80μm signal and 4.45 μm idler under pumping power of 28. 7 W. The slope efficiency reaches 61.8%, and M^2 = 3.6 for OPO output is obtained.     

“技术增加值”评价原理与方法

提出了"技术增加值"的概念,认为公司价值不仅包括"经济增加值",还应包括"技术增加值".在系统地比较了"经济增加值"与"技术增加值"两个概念和形成过程的基础上,给出了技术增加值的评价模型、评价方法和评价步骤,最后通过两个应用示例予以说明.提出应用"技术增加值"指标,更加客观反映企业的全面价值和业绩.     

TiO2掺杂ZnO-Bi2O3-Co2O3-MnCO3系低压压敏陶瓷的微结构和电性能研究

采用固相反应法制备了TiO2掺杂的ZnO-Bi2O3-Co2O3-MnCO3系低压压敏陶瓷.采用X射线衍射、扫描电镜、压敏电阻直流参数仪、阻抗分析仪等研究了掺杂量对陶瓷的微结构、压敏性能和阻抗等影响.结果表明:掺杂1.0mol;TiO2时综合电性能最好,压敏电压梯度为21.6 V/ mm,漏电流密度为0.02 μA/ mm2,非线性系数为33;掺杂最大于1.0 mol;时,压敏电压梯度降低的同时也使非线性系数降低,漏电流密度增大;Cole-Cole形式的复阻抗谱图表明掺杂1.0 mol;TiO2的晶界电阻最大,晶界电阻对ZnO-Bi2O3-Co2O3-MnCO3-TiO2系低压压敏陶瓷电阻的贡献最为明显.     

NiY分子筛选择性吸附脱硫性能及作用机理

用液相离子交换法制备了NiY分子筛,并用XRD、TEM、ICP、N2吸附和吡啶吸附原位红外技术等表征手段对其进行了表征. 利用固定床、气相色谱-硫发光检测器（GC-SCD）及傅里叶红外光谱（FT-IR）等方法系统研究了NiY分子筛对噻吩、2-甲基噻吩、3-甲基噻吩、四氢噻吩、苯并噻吩、二苯并噻吩、4-甲基二苯并噻吩、4,6-二甲基二苯并噻吩8种有机硫化物的选择性吸附脱硫性能和吸附机理. 结果表明,NiY分子筛对硫化物的穿透吸附硫容量顺序为四氢噻吩﹥苯并噻吩≈二苯并噻吩≈4,6-二甲基二苯并噻吩﹥4-甲基二苯并噻吩﹥2-甲基噻吩≈3-甲基噻吩﹥噻吩,说明有机硫化物的空间位阻效应不是其在NiY分子筛上吸附的决定因素. 红外结果表明,不同硫化物与NiY分子筛的作用机理并不相同,但主要以硫原子与金属离子配位作用（S-M作用）为主. 噻吩及其烷基取代物在NiY吸附剂上表面酸性作用下发生催化反应,噻吩环的共轭体系遭到破坏形成硫化物大分子或聚合物,导致分子筛孔道的堵塞,严重影响吸附剂的吸附脱硫能力. NiY的选择性吸附脱硫性能是硫化物与吸附中心的作用模式及吸附剂表面酸性综合作用的结果.     

PS-b-P (DMS-stat-VMS)嵌段聚合物的制备及性能

采用活性阴离子聚合方法,以仲丁基锂为引发剂,以苯乙烯、六甲基环三硅氧烷（D3）和2,4,6-三乙烯基-2,4,6-三甲基环三硅氧烷（V3）为反应单体,分步聚合制备了聚苯乙烯-b-聚（二甲基硅氧烷-stat-乙烯基甲基硅氧烷）[PS-b-P（DMS-stat-VMS）]嵌段聚合物.采用傅里叶变换红外光谱、氢核磁共振谱及凝胶渗透色谱对共聚物的化学结构、分子量及分子量分布进行了表征,并通过扫描电子显微镜、原子力显微镜及接触角等测试方法研究了共聚物各链段组分对共聚物形貌及表面亲疏水/油性的影响.结果表明,所制备的共聚物分子量分布较窄,由于各组分性能的差异而呈现出微相分离结构,同时该共聚物保留了PS-b-PDMS原有的表面性质,为设计结构多样性及性能优异的聚硅氧烷共聚物提供了新思路.     

Passively Q-Switched Tm,Ho：YVO4 Laser with Cr：ZnS Saturable Absorber at 2 μm

A stable diode-pumped passively Q-switched Tm,Ho：YVO4 laser with Cr：ZnS saturable absorber is reported. The shortest pulse duration of -500 ns with the central wavelength of 2041 nm is obtained at the pump power of 7.4 W, corresponding to the pulse energy of 3.5 μd at repetition rate of 65 kHz.     

A Diode-Pumped 1617 nm Single Longitudinal Mode Er：YAG Laser with Intra-Cavity Etalons

We demonstrate the continuous wave p-polarized single longitudinal mode （SLM） operation of an Er：YAG laser at 1617.6nm pumped by a diode-laser with three inserted Fabry-Perot （FP） etalons at room temperature. The Brewster angle inserted FP is applied to obtain the p-polarized laser. For free running, the maximum output power is 570 m W with a pump power of 12.5 W. An incident pump power of 12.5 W is used to generate the maximum p-polarized single longitudinal mode output power of 78.5 m W, corresponding to a slope efficiency of 1.6% and an optical-to-optical efficiency of 0.61%. The beam quality M2 is measured to be 1.15 at the highest SLM output power. This stable polarized SLM oscillation is encouraging due to its application for an injection-locked system used as a master laser.     

Predicting the growth of new links by new preferential attachment similarity indices

By revisiting the preferential attachment (PA) mechanism for generating a classical scale-free network, we propose a class of novel preferential attachment similarity indices for predicting future links in evolving networks. Extensive experiments on 14 real-life networks show that these new indices can provide more accurate prediction than the traditional one. Due to the improved prediction accuracy and low computational complexity, these proposed preferential attachment indices can be helpful for providing both instructions for mining unknown links and new insights to understand the underlying mechanisms that drive the network evolution.     

紫外光引发剂907及其反应中间体的气相色谱测定

建立了光引发剂907合成工艺控制中反应原料、中间体及产物的气相色谱分析方法。采用SE-54石英毛细管柱,程序升温进行分离,氢火焰离子化检测器(FID)进行检测。结果表明,原料苯甲硫醚,反应中间体807A、807B、907C和产物907线性范围分别为0.2～14.0μg/mL、0.4～20.0μg/mL、0.5～22.0μg/mL和0.6～19.0μg/mL,线性相关系数R均大于0.999,相对标准偏差小于2.5%,回收率为93.6%～106.8%。产物结构通过红外光谱进行表征。该方法线性关系、准确度和精密度良好,适用于光引发剂907合成工艺的快速监控及产品定量分析。     

Theoretical Studies on the Proton Transfer Mechanism in Four-water Hydrated Glycine Complexes

The mp2/6-31++g**//b3lyp/6-31++g** method has been employed to study the proton transfer mechanism in 4H2O-glycine complexes(4W-G).Compared with bare glycine the four-water hydrated neutral glycine complexes(4W-GN) can turn into the corresponding zwitterionic glycine(4W-GZ) through proton transfer.The most stable conformation of 4W-GZ has a "double water-chain" structure and is more stable than its corresponding precursor 4W-GN by 0.97 KJ/mol though it is less stable than the most stable 4W-GN by 7.80 KJ/mol.It is a spontaneous reaction to form the most stable conformation of 4W-GZ,and the potential barrier is only 1.97 KJ/mol,so the probability of this reaction is very high and the most stable 4W-GZ may be detected in experiment or in the early stage of experiment.