电子自旋共振年代计时(III)——关于鹿牙和牛牙化石的研究

采用电子自旋共振年代计时方法测定了贵州桐梓马鞍山的鹿牙化石及河北迁安爪村牛牙化石的年龄,它们分别为(1.5±0.2)×10~4a和(3.7±0.5)×10~4a。在研究作为ESR信号来源的顺磁缺陷中心的性质时,还应用了正电子湮没技术。     

浅谈城市道路沥青路面下封层的作用及施工工艺

从沥青路面下封层的主要作用及原理出发，阐述了城市道路沥青路面设置下封层的必要性及常用的施工工艺。     

图书史研究中需要注意的几个问题

从图书馆学的角度出发,对中国图书史研究过程中需要注意的几个问题,如旋风装新旧说之争、造纸术和雕版印刷术的发明时间等予以了分析和探讨,最后提出了自己的倾向性的观点。     

The stopped-flow technique in analytical chemistry

A critical survey of the stopped-flow technique is presented. The instrumentation typically used and the scope of its analytical applications are discussed. The stare-of-the-art of this technique and its wide possibilities in routine analyses are also considered.     

Living radical emulsion polymerization using the nanoprecipitation technique: An extension to atom transfer radical polymerization

Living radical polymerizations of styrene were performed under emulsion atom transfer radical polymerization conditions with latexes prepared by a nanoprecipitation technique recently developed for the stable free‐radical polymerization process. Latexes were prepared by the precipitation of a solution of low‐molecular‐weight polystyrene in acetone into a solution of a surfactant in water. The resulting particles were swollen with styrene and then heated. The effects of various surfactants and hydrophobic ligands, the reaction temperature, and the ligand/copper(I) bromide ratio were studied. The best results were obtained with the nonionic surfactant Brij 98 in combination with the hydrophobic ligand N,N‐bis(2‐pyridylmethyl)octadecylamine and a ligand/copper(I) bromide ratio of 1.5 at a reaction temperature of 85–90 °C. Under these conditions, latexes with good colloidal stability with average particle diameters of 200 nm were obtained. The molecular weight distributions of the polystyrenes were narrow, although the experimental molecular weights were slightly larger than the theoretical ones because not all the macroinitiator appeared to reinitiate. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4027–4038, 2006     

A bidirectional hybrid DWDM-PON employing optical injection locking technique and data comparators

A bidirectional hybrid dense-wavelength-division-multiplexing (DWDM)-passive optical network (PON) employing optical injection locking technique on vertical-cavity surface-emitting lasers (VCSELs) and data comparator, as well as optical injection locking technique on distributed feedback laser diodes (DFB LDs) and amplitude/phase compensator is proposed and demonstrated. Improved performances of bit error rate (BER) and carrier-to-noise ratio/composite second order/composite triple beat (CNR/CSO/CTB) were observed in our proposed bidirectional hybrid DWDM-PON. Bidirectional transmission in bidirectional hybrid DWDM-PON architecture is a very attractive option, the capacity of the optical network can be expanded relatively easily by bidirectional transmission technology.     

海洋气象观测技术研发进展

 海洋覆盖地球70%以上的面积,由于没有陆地上布设气象观测站网的便利性,使得海上气象观测资料严重不足,难以支撑对海上和来自海上高影响天气过程的深入研究以及预报准确性的提高。为了加强海上气象观测能力的建设,本文对气象海洋卫星、大气探测飞机、岛屿气象站、海上浮漂和岸基雷达等观测平台及技术进行了综述,并对未来基于无人驾驶平台的智能海洋气象探测技术进行展望。     

Influence of aliphatic spacer group on adsorption mechanisms of phosphonate derivatives of l-phenylalanine: Surface-enhanced Raman, Raman, and infrared studies

The nature of phosphonopeptides containing N-terminal l-phenylalanine (l-Phe), namely l-Phe-dl-NH-CH(CH(CH₃)₂)-PO₃H₂ (A), l-Phe-l-NH-CH(CH₃)-PO₃H₂ (B), and l-Phe-dl-NH-CH(CH₂CH₂COOH)-PO₃H₂ (C) (Fig. 1 presents molecular structure of these molecules), adsorbed on electrochemically roughened and colloidal silver surfaces has been explored by surface-enhanced Raman spectroscopy (SERS). To reveal adsorption mechanism of these species on the basis of their SERS spectra at first Fourier-transform Raman (FT-RS) and absorption infrared (FT-IR) spectra of non-adsorbed molecules were measured. Examination of enhancement, frequency shifts, and changes in relative intensities of SERS bands due to adsorption and surface roughens variation reveals that the tilted compounds adsorb on the electrochemically roughened silver substrate in similar way, while they behave differently on the colloidal silver surface. A stronger enhancement of in-plane ring vibrations of the l-Phe ring, i.e., ν₃ and ν_18b (B₂), over these of the A₂ symmetry in all SERS spectra on the electrochemically roughened silver substrate suggests that the ring interacts with this surface adopting slightly deflect orientation from the perpendicular one. Also, enhancement of PO and -CH₂-/-CH₃ fragments vibrations points out that they are involved in adsorption process on this substrate. This conclusion was drawn on the basis of the enhancement of 1274-1279 and 1138-1152 (ν(PO)), 1393-1400 (δ(CH) + ρ_b(CNH₂) + ν(C-C_O) + δ(CH₃)), ∼1455 (δ(CCH₃/CCH₂) + ρ_b(CH₃/CH₂), and 1505-1512 cm⁻¹ (δ(CH₂) + Phe(ν_19a)) bands. Although a relative intensity ratio of these bands in the presented SERS spectra is different. On the other hand, on the colloidal silver nanoparticles, the aromatic ring of all molecules is lying flat or takes almost parallel orientation to this surface. Besides, A interacts also via P-terminal group (568, 765, 827, 1040, and 1150 cm⁻¹), whereas B mainly through NH₂-C-(CO)-CNH-(712 and 1255 cm⁻¹). In the case of C, it adsorbs on the silver colloidal surface mainly through the aromatic ring of l-Phe, while other fragments of the molecule are in close proximity to this surface as comes off the weak enhancement of bands due to the aliphatic vibrations.     

Adsorption mechanism of physiologically active l-phenylalanine phosphonodipeptide analogues: Comparison of colloidal silver and macroscopic silver substrates

Here we present SERS spectra of several l-phenylalanine (Phe) phosphonodipeptides, i.e., l-Phe-l-Ala-PO₃H₂ (MD1), l-Phe-l-Val-PO₃H₂ (MD2), l-Phe-β-Ala-CH(OH)-PO₃H₂ (MD3), l-Phe-l-Ala-CH(OH)-PO₃H₂ (MD4), l-Ala-(3,4-dimethoxy)-l-Phe-PO₃H₂ (MD5), and l-Ala-(3,4-dimethoxy)-(des-CH₂)-l-Phe-PO₃H₂ (MD6), immobilized on electrochemically roughened silver electrodes. These spectra are analyzed by theoretical calculations using density functional theory (DFT) at the B3LYP level with 6-31++G∗∗ basis set. In addition, these spectra are compared with SERS spectra of these species adsorbed on a colloidal silver surface. We showed that on the macroscopic silver substrate, the Phe aromatic ring of MD3 and MD4 is oriented vertically, while for MD1 it almost “stands up” on this surface. In the other three cases, the Phe ring adopts a tilted orientation in regard to the substrate. We also find that the phosphonate , methyl/methane, or dimethoxy groups of MD1, MD2, MD3, MD5, and MD6 are involved in the interaction of these phosphonodipeptides with the electrochemically roughened surface. This phenomenon is clearly seen for -CH₂-/-CH₃/-OCH₃ moieties as well as for the group that adsorbs on the macroscopic silver substrates mainly via the PO fragment. We also showed that MD4 binds to the macroscopic silver substrate through the hydroxyl, amine, and phosphonate groups, while the methylene/methane moieties are remote from this surface. We found that studied phosphonodipeptides often adsorb differently on the macroscopic silver substrate and on the colloidal silver nanoparticles. For example, MD1 adopts an almost vertical orientation on the electrochemically roughened silver substrate and is tilted or close to flat on the silver nanoparticles.