碘化物升华分离-电感耦合等离子体光谱法测定土壤和沉积物中砷、锑、铋、镉、锡

将土壤或水系沉积物样品与固体NH4I按1:0·25的比例在双球玻璃管中混匀后在苯灯喷焰上加热,使样品中的As,Sb,Bi,Cd和Sn转变为碘化物升华逸出而与基体分离,挥发物用盐酸溶解后用电感耦合等离子体光谱法(ICP-AES)测定。实验探讨了NH4I的用量、挥发和溶解条件,光谱测定条件,内标选择,测定谱线选择及背景和谱线干扰校正。用土壤和水系沉积物国家一级标准物质验证了方法的准确性和精密度,测定结果与标准值吻合。方法快速简便,结果可靠,检出限为0·01～0·35μg·g-1,适用于地球化学勘探大批量土壤和沉积物样品中As,Sb,Bi,Cd和Sn的测定。     

Application of Inductively Coupled Plasma-Atomic Emission Spectrometry/Mass Spectrometry to Phase Analysis of Gold in Gold Ores

Inductively coupled plasma-atomic emission spectrometry/mass spectrometry (ICP-AES/MS) is a potentially powerful tool in chemical phase analysis of gold in batch mode, especially applicable to the low-grade gold ores with gold content of far below detection limit of the other methods, but it has not been used in gold phase analysis of gold ores. In this work, three types of typical gold deposits (altered rock type, quartz vein type, and microscopic disseminated type) and national standard reference materials of gold ores were used to establish and validate a method for gold phase analysis of gold ores using ICP-AES/MS. The optimum conditions of phase analysis were determined, including the sample granularity and preparation procedures, separation absorbent, pretreatment procedures of various phases of gold and optimized instrument parameters. Evaluation of the optimized method showed that this method had acceptable precision (RSD: 1.1%–10.6%) and accuracy (relative error, RE: 0.5%–6.3%), and the detection results of gold in ores were comparable with those obtained using the hydroquinone volumetric method-extraction flame atomic absorption spectrometry (VOL-AAS) and graphite furnace atomic absorption spectrometry (GFAAS) methods. The sum content of gold of the 4 phases (free gold, F_Au; linked gold, L_Au; sulphide-bearing gold, S_Au; and other mineral-bearing gold, A_Au) conformed to the total gold content and was consistent with the results of rock-mineral identification. The proposed method had a low detection limit (0.30 ng g^–1) and wide linear range (5.0 ng mL^–1–20.00 μg mL^–1). It is a simple, rapid, and efficient method for gold phase analysis in batch form.     

Preparation and Characterization of Room-temperature Ferromagnetic Ni-doped TiO2 Nanobelts

Ni-doped anatase TiO₂ nanobelts (NBs) with different Ni²⁺ contents were simply prepared by combining ion-exchange with hydrothermal treatment. They were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR), and magnetic measurement techniques. The results showed that Ni²⁺ cations doped into the TiO₂ lattice and no metallic nickel clusters or nanoparticles could be found. The magnetic results demonstrated that the prepared Ni-doped TiO₂ samples had complex magnetic mechanism including room-temperature ferromagnetic and paramagnetic behaviors, and with the increase of Ni²⁺ content, the magnetization also increased under the same applied field owing to uniform distribution of Ni²⁺ ions in TiO₂ nanobelts.     

毛细管区带电泳技术快速分离检测爆炸残留物中的无机离子

利用间接紫外毛细管区带电泳方法完成了对爆炸残留物中7种无机离子(K+,NH+4,NO-2,NO-3,SO2-4,ClO-3,ClO-4)的分离检测。阳离子测定采用的缓冲体系为10 mmol/L吡啶（pH 4.5）-3 mmol/L冠醚,K+和NH+4在2.6 min内达到基线分离,检出限分别为0.25 mg/L和0.10 mg/L(S/N=3)。阴离子测定采用的缓冲体系为40 mmol/L硼酸-1.8 mmol/L重铬酸钾-2 mmol/L硼酸钠（pH 8.6）,氢氧化四甲铵为电渗流改性剂,5种阴离子在4.6 min内达到基线分离,检出限为0.10～1.85 mg/L。该方法已成功地应用于实际爆炸物样品种类的判定分析,取得了很好的结果。     

Surface-enhanced Raman scattering system of sample molecules in silver-modified silver film

Surface-enhanced Raman scattering (SERS) spectrum of very good quality of "silver nano-particles/sample molecules/silver film" system was reported by nesting the sample molecules to the gap of silver nano-particles and silver film, indicating that "silver nano-particles/sample molecules/silver film" is a highly SERS-active system. Not only was the number of the vibrational modes increased, but also were the frequencies of Raman bands up and down shifted. It is difficult to separate the contributions of the electromagnetic and chemical mechanisms to the great enhancement of the Raman signal. The shift by 5-30cm(-1) of the SERS bands and the change in their relative intensity compared with the ordinary Raman spectrum indicate the chemisorption of the sample molecules on the silver-modified silver surface. Furthermore, the silver nano-particles modified on the rough silver film surface play an important role in magnifying the surface local electric field near the silver surface through resonant surface plasmon excitation. From the rich information, obtained from high-quality SERS of PHBA in ternary system, we inferred that PHBA molecules in ternary system adsorb onto the metal surfaces through carboxyl at a perpendicular orientation.     

Adsorption orientations and interactions of methyl orange on negatively and positively charged colloidal silver particles

Both positively and negatively charged colloidal silver particles were prepared from chemical deoxidized methods. Then UV-visible absorption, fluorescence, and surface-enhanced Raman scattering of methyl orange adsorbed onto surfaces of these two kinds of particles were observed and compared with each other. The results indicate that dye molecules may adsorb onto these two kinds of silver surface in differing adsorption orientations with different interactions, which caused the different phenomena.     

Simple method for electrochemical preparation of silver dendrites used as active and stable SERS substrate

This paper reports that a new SERS-active silver film on the surfaces of a series of electric material has been prepared by an electrochemical technique in an aqueous solution of AgNO(3). With scanning electron microscopy, the morphology of the silver film is a treelike structure. By SERS measurements, the film of silver dendrites is shown to be an excellent substrate, demonstrating significant enhancement effect, spatial uniformity and good stability. As the fabrication process of this substrate is very simple and inexpensive, it is proposed that this method may be used in large-scale preparation of substrates that have been widely applied in Raman analysis.     

A Representation of the Lorentz Spin Group and Its Application

For an integer m ≥ 4, we define a set of 2[m/2] × 2[m/2] matrices γj （m）, （j = 0, 1,..., m - 1） which satisfy γj （m）γk （m） ＋γk （m）γj （m） = 2ηjk （m）I[m/2], where （ηjk （m）） 0≤j,k≤m-1 is a diagonal matrix, the first diagonal element of which is 1 and the others are -1, I[m/2] is a 2[m/1] × 2[m/2] identity matrix with [m/2] being the integer part of m/2. For m = 4 and 5, the representation （m） of the Lorentz Spin group is known. For m≥ 6, we prove that （i） when m = 2n, （n ≥ 3）, （m） is the group generated by the set of matrices {T｜T=1/√ξ（（I＋k） 0 ＋ 0 I-K） （ U 0 0 U）, （ii） when m = 2n ＋ 1 （n≥ 3）, （m） is generated by the set of matrices {T｜T=1/√ξ（I -k^- k I）U,U∈ （m-1）,ξ=1-m-2 ∑k,j=0 ηkja^k a^j〉0, K=i[m-3 ∑j=0 a^j γj（m-2）＋a^（m-2） In],K^-=i[m-3∑j=0 a^j γj（m-2）-a^（m-2） In]}     

Second Order Correction of Relativistic Optical Potential

The imaginary part of the off-energy shell optical potential of a nucleon in nuclear matter, where the polarization and correlation contribution of the exchanges of the σ and ω mesons are taken into account, is derived in the framework of the relativistic meson-nucleon field theory. The second order correction of the real part of the optical potential is calculated in terms of the dispersion relation and the effective mass of a nucleon in the nuclear medium is also investigated in this paper.     

第四类超Cartan域的Bergman核函数

显式给出了第四类超Cartan域的Bergman核函数及其全纯自同构群．