200KV重离子加速器及其应用

本文介绍一台采用双潘宁型多电荷重离子源的200kV重离子加速器,简述它在GaP光探测器的研制、聚合物材料和金属材料的离子注入改性等方面的研究与应用。     

氧化环己烯连续进料下二氧化碳-环氧丙烷-氧化环己烯三元共聚物的合成

由于氧化环己烯（CHO）与二氧化碳的共聚反应速度比其与环氧丙烷（PO）快,这种竞聚率的差异导致一锅法所得的二氧化碳-环氧丙烷-氧化环己烯三元共聚物的组成难以稳定控制。 为此本文在稀土三元催化剂下,采用氧化环己烯单体连续进料的方法合成了二氧化碳-环氧丙烷-氧化环己烯三元共聚物,催化效率可达575 g/(mol Zn h)。 三元共聚物的玻璃化转变温度随CHO含量升高而增大,当CHO的摩尔投料比从0.19增加到0.59时,玻璃化温度从44.3 ℃提高到70.1 ℃。 CHO连续进料合成的三元共聚物的组成与投料比基本相近,且连续进料法所合成的三元共聚物只有一个玻璃化转变温度,而普通的一锅法所得的三元共聚物通常存在两个玻璃化转变温度,因此连续进料法是制备组成稳定的二氧化碳-环氧丙烷-氧化环己烯三元共聚物的有效方法。     

顶空气相色谱法测定甲氧苄啶中的残留丙烯腈

采用顶空进样模式,以HP-624毛细管色谱柱为分离柱,二甲亚砜为溶剂,氮气作载气,FID为检测器,用气相色谱法测定甲氧苄啶中的残留丙烯腈。丙烯腈的线性范围为0．25～200．10μg,相关系数为0．9999,检出限为0.05μg,测定结果的相对标准偏差为3．4％,平均回收率为100．5％。     

Auto-deposition of 210Bi and 210Po on nickel discs and their application in the analysis of natural waters

Journal of Radioanalytical and Nuclear Chemistry - This study presents a time-efficient method of analysing 210Pb, 210Bi, and 210Po in natural waters. The optimum pH (1.00), temperature...     

An isometrical CPn-theorem

Let M^n(n\ge \mathrm{3}) be a complete Riemannian manifold with {{\displaystyle \sec ?}}_M\ge \mathrm{1}, and let {{\displaystyle M}}_i^{{{\displaystyle n}}_i}(i=\mathrm{1},\mathrm{2}) be two complete totally geodesic submanifolds in M. We prove that if n₁ + n₂ = n − 2 and if the distance \left|{{\displaystyle M}}_{\mathrm{1}}{{\displaystyle M}}_{\mathrm{2}}\right|\ge \pi /\mathrm{2}, then M_i is isometric to {\mathbb{S}}^{{{\displaystyle n}}_i}/{{\displaystyle \mathrm{?}}}_h,{\mathrm{?}\mathrm{P}}^{{{\displaystyle n}}_i/\mathrm{2}}/{{\displaystyle \mathrm{?}}}_{\mathrm{2}}, or {\mathrm{?}\mathrm{P}}^{{{\displaystyle n}}_i/\mathrm{2}}/{{\displaystyle \mathrm{?}}}_{\mathrm{2}} with the canonical metric when n_i>0, and thus, M is isometric to {\mathbb{S}}^n/{{\displaystyle \mathrm{?}}}_h,{\mathrm{?}\mathrm{P}}^{n/\mathrm{2}}, or {\mathrm{?}\mathrm{P}}^{n/\mathrm{2}}/{{\displaystyle \mathrm{?}}}_{\mathrm{2}} except possibly when n = 3 and M₁ (or M₂) \stackrel{\mathrm{i}\mathrm{s}\mathrm{o}}{{\displaystyle \cong }}{\mathbb{S}}^{\mathrm{1}}/{{\displaystyle \mathrm{?}}}_h with h\ge \mathrm{2} or n = 4 and M₁ (or M₂) \stackrel{\mathrm{i}\mathrm{s}\mathrm{o}}{{\displaystyle \cong }}\mathrm{?}{\mathrm{P}}^{\mathrm{2}}.     

Effects of ammonium citrate additive on crystal morphology of aluminum phosphate ammonium taranakite

In this communication, we demonstrated the growth of aluminum phosphate ammonium taranakite (NH₄-AlPO₄) crystals from regular hexagonal form into the disk-like form could be controlled by ammonium citrate (AMC) as the effective crystal growth modifier at 90 °C. Prepared crystals were characterized by field emission scanning electron microscopy (SEM) and X-ray diffraction (XRD). The effects of AMC's concentration on the crystal form and morphology of NH₄-AlPO₄ were studied. The results showed that the AMC's concentration is an important parameter to control the size and morphology of NH₄-AlPO₄ crystal. The formation mechanism of the special morphology of NH₄-AlPO₄ crystals was also analyzed.     

低光泽度印刷色谱色貌数据组的建立与评价

色貌预测是现代颜色科学领域的基本理论和技术。为了评价低光泽度彩色印刷色谱的色貌,以丽印胶版纸印制的彩色印刷色谱为研究对象,根据颜色科学和心理物理学相关实验,建立其色貌参数样本数据组。采用相对系数R2和差异系数CV等数理统计方法,评价这种印刷色谱中Y-M内页在三种不同的照明光源下色貌的视觉评估结果。实验数据分析表明,在D65、A和TL84三种光源中,人眼在A光源下对颜色的识别能力明显不同于D65和TL84光源;同样在这三种光源中人眼对明度和色调的评估准确度最高,彩度最差。     

Nickel-catalyzed C-H direct amination of benzoxazoles with secondary amines

In this article, a facile, efficient and practical method for Ni-catalyzed direct C-H amination of benzoxazole with secondary amines has been developed. This procedure requires Ni(OAc)(2)·4H(2)O as catalyst, TBHP as oxidant and acid as the additive. A variety of substituted benzoxazol-2-amines were synthesized in moderate to good yields.     

Synthesis and properties of reactive liquid crystal monomers and side-chain liquid crystalline polymers

Two nematic liquid crystal (LC) monomers containing double bonds in the side chain were designed and synthesised. Length of the side groups varied from 1 to 2 methylene units. The side-chain polymers were synthesised by hydrosilylation reaction. The molecular structures of the intermediates and the LC monomers were characterised by Fourier transform infrared, elemental analysis and nuclear magnetic resonance spectroscopy. The thermal phase behaviour of the monomers and polymers were investigated by differential scanning calorimetry and polar optical microscopy coupled with hot stage. The LC monomers showed only one nematic mesophase in the cooling process. And, the two polymers exhibit an enantiotroppic nematic mesophase either in the heating or in the cooling process.     

Cobalt(II)–catalyzed C8H alkoxylation of 1-naphthylamine derivatives with alcohols

An efficient protocol for cobalt (II)-catalyzed regioselective aryl C8H bond alkoxylation of 1-naphthylamine derivatives with readily available alcohols has been developed, demonstrating an efficient approach to 8-alkoxy-1-naphthylamine derivatives with good functional group tolerance. Note that the picolinamide moiety as a bidentate directing group may play a key role in this regioselective transformation.