太阳光泵浦激光器侧面泵浦效率的提高

太阳光泵浦激光器直接利用太阳光作为泵浦源,实现了太阳光能量到激光能量的直接转化。设计了分腔水冷型金属锥形泵浦腔,以直径8 mm,长115 mm的Nd:YAG晶体棒作为激光工作物质,用有效面积1.03 m2菲涅尔透镜会聚太阳光,实验获得了23.7 W的稳定激光输出,斜效率为7.87%。通过对比实验,改进后的分腔水冷型太阳光泵浦激光器较原有锥形腔激光器有55.92%的激光输出功率提升。分别从侧面泵浦光在冷却水中的吸收损耗以及其耦合效率等方面对新型腔体结构进行了分析,证实了分腔水冷型腔体结构对侧面泵浦效率的提高,并提出了陶瓷漫反射材质的分腔水冷型激光腔的设计。     

Catalytic effect of water,water dimer,water trimer,HCOOH, H2SO4, CH3CH2COOH and HN(NO2)2 on the isomerisation of HN(NO2)2 to O2NNN(O)OH: a mechanism study

In this article, the isomerisation mechanisms of HN(NO₂)₂ to O₂NNN(O)OH without and with catalyst X (X = H₂O, (H₂O)₂, (H₂O)₃, HCOOH, H₂SO₄, CH₃CH₂COOH and HN(NO₂)₂) have been investigated theoretically at the CBS-QB3 level of theory. Our results show that the catalyst X (X = H₂O, (H₂O)₂, (H₂O)₃, HCOOH, H₂SO₄ and CH₃CH₂COOH) shows different positive catalytic effects on reducing the apparent activation energy of the isomerisation reaction processes. Such different catalytic effects are mainly related to the number of hydrogen bonds and the size of the ring structure in X (X = H₂O, (H₂O)₂ and (H₂O)₃)-assisted transition states, as well as different values of pK_a for H₂SO₄, HCOOH and CH₃CH₂COOH. Very interesting is also the fact that H₂SO₄-assisted reaction is the most favourable for the hydrogen transfer from HN(NO₂)₂ to O₂NNN(O)OH, due to the smallest pK_a (?3.0) value of H₂SO₄ than H₂O, HCOOH, H₂SO₄ and CH₃CH₂COOH, and also because of the largest ∠X???H???Y (the angle between the hydrogen bond donor and acceptor) involved in H₂SO₄-assisted transition state. Compared to the self-catalysis of the isomerisation mechanisms of HN(NO₂)₂ to O₂NNN(O)OH, the apparent activation energy of H₂SO₄-assisted channel also reduces by 9.6 kcal?mol^?1, indicating that H₂SO₄ can affect the isomerisation of HN(NO₂)₂ to O₂NNN(O)OH, most obvious among all the catalysts H₂O, (H₂O)₂, (H₂O)₃, HCOOH, H₂SO₄, CH₃CH₂COOH and HN(NO₂)₂.     

158A?GeV/c?Pb+Pb碰撞中J/ψ是反常压低吗?

用含有领头粒子能量衰减、J/ψ先驱体在弦色场中离解和物理J/ψ的强子吸收等三种机制的强子和弦级联模型,JPCIAE,计算了200AGeV/c的PA和AB轻的弹核)反应以及Pb+Pb反应中J/ψ压低因子,取得与NA38及NA50数据全面地较好符合; 从而对Pb+Pb反应中J/ψ是反常压低的说法提出质疑.     

金纳米星诊疗剂的光热特性及其在光热治疗和光学相干层析成像中的应用研究

为了开发一种优异的用于光热治疗和光学相干层析成像的金纳米星诊疗剂,对金纳米星的制备、光热特性以及光热治疗和光学相干层析成像中的应用进行研究.利用尖端结构增强金纳米材料的局域表面等离子体共振特性,通过种子介导法制备了多枝化的金纳米星,多尖端的结构使其具有明显的光热效果,并探究了其作为光热治疗的诊疗剂和光学相干层析成像造影...     

黄河河道冰水情定点连续自动检测及数据分析

根据黄河中上游流域冰水情监测以及预防凌汛灾害的需求,设计了一种适合黄河河道的冰水情自动测报系统.该系统由基于空气、冰与水电阻特性差异的冰层厚度传感器、DS18B20的温度梯度传感器以及智能处理仪构成.采用该系统在内蒙托克托县黄河河道进行了黄河封冻期河道冰层厚度连续监测试验,获取了大量的现场实测数据,对采样数据进行分析,提出了判别冰层厚度的平均滤波算法,实现了对冰层生消变化全过程的自动监测.     

Phase behavior and interfacial properties of diblock copolymer-homopolymer ternary mixtures: Influence of volume fraction of copolymers and interaction energy

We use a Monte Carlo method to study the phase and interfacial behaviors of A-b-B diblocks in a blend of homopolymers, A and B, which are confined between two asymmetric hard and impenetrable walls. Our results show that, when the interaction strength is weak, the block copolymersare uniformly distributed in the ternary mixtures under considered concentrations. Under strong interaction strength, distribution region of the block copolymers changes from a single smooth interface to a curved interface or multi-layer interface in the ternary mixtures. Furthermore, our findings show that with increasing volume fraction of A-b-B diblock copolymer(фC), copolymer profiles broaden while фC≥ 0.4, a lamellar phase is formed and by further increasing фC, more thinner layers are observed. Moreover, the results show that, with the increase of фC, the phase interface first gradually transforms from plane to a curved surface rather than micelle or lamellar phase while with the increase of the interaction between A and B segments(ε_(AB)), the copolymer chains not only get stretched in the direction perpendicular to the interface, but also are oriented. The simulations also revealthat the difference between symmetric and asymmetric copolymers is negligible in statistics if the lengths of two blocksare comparable.     

物理实验中温度测量的改进与应用

本分析了物理实验中玻璃温度计进行测温所存在的问题,根据半导体温度传感器工作原理设计并制作了一种新型的电子测温仪,该仪器具有精度高、响应快、读数方便以及便于二次开发等优点。     

Facile RAFT precipitation polymerization for the microwave-assisted synthesis of well-defined, double hydrophilic block copolymers and nanostructured hydrogels

Water-soluble macromolecular chain transfer agents (Macro-CTAs) were developed for the microwave-assisted precipitation polymerization of N-isopropylacrylamide. Two types of Macro-CTAs, amphiphilic (Macro-CTA1) and hydrophilic (Macro-CTA2), were investigated regarding their activity for the facile formation of nanoparticles and double hydrophilic block copolymers by RAFT processes. While both Macro-CTAs functioned as steric stabilization agents, the variation in their surface activity afforded different levels of control over the resulting nanoparticles in the presence of cross-linkers. The cross-linked nanoparticles produced using the amphiphilic Macro-CTA1 were less uniform than those produced using the fully hydrophilic Macro-CTA2. The nanoparticles spontaneously formed core-shell structures with surface functionalities derived from those of the Macro-CTAs. In the absence of cross-linkers, both types of Macro-CTAs showed excellent control over the RAFT precipitation polymerization process with well-defined, double hydrophilic block copolymers being obtained. The power of combining microwave irradiation with RAFT procedures was evident in the high efficiency and high solids content of the polymerization systems. In addition, the "living" nature of the nanoparticles allowed for further copolymerization leading to multiresponsive nanostructured hydrogels containing surface functional groups, which were used for surface bioconjugation.