Temperature measurement of a single ion in a Penning trap

The present work is concerned with the association of a temperature to a single ion stored in a Penning ion trap. Several methods are described which allow to determine the temperature by measurements of the ions cyclotron and axial trapping frequencies. Recent results of a measurement on a hydrogen-like carbon ion ¹²C^{5 +} by use of mode coupling are presented and possible further applications are discussed.Received: 8 July 2004, Published online: 6 December 2004PACS: 07.20.-n. Thermal instruments and apparatus - 07.20.Dt. Thermometers - 42.50.Lc Quantum fluctuations - 42.50.Vk Mechanical effects of light on ions     

The anomalous magnetic moment of the electron in hydrogenlike ions

The precise determination of the anomalous magnetic moment of the electron bound in hydrogen-like ions allows for a stringent test of quantum electrodynamics (QED)in the presence of strong electric fields. g-factor measurements on the electron bound in hydrogen-like ions ¹²C⁵⁺ and ¹⁶O⁷⁺, using single ions confined in a Penning trap, have yielded values in agreement with theory on the ppb level. If the QED calculations are considered correct, the results can in turn be used for a determination of fundamental constants like the electron mass m_e, the fine structure constant α or nuclear parameters. We report about presentdevelopments towards g-factor measurements also in medium-heavy and heavy highly-charged ions.     

A Possible New Value for the Electron Mass from g-Factor Measurements on Hydrogen-Like Ions

The mass of the electron in atomic units (m _e) represents the largest error contribution in an experiment to determine the g-factor of the electron bound in hydrogen-like carbon. Recent progress in the calculation reduces the uncertainty of the theoretical value to such a low value that m _e can be determined from a comparison of experimental and theoretical g-factors. The present preliminary value of the electron mass agrees with the accepted value but reduces the uncertainty by about a factor 2. This revised version was published online in July 2006 with corrections to the Cover Date.     

Mössbauer analysis of coal coke samples from Samacá, Boyacá, Colombia

Three samples of coke produced from coal from a mine in the municipality of Samacá, department of Boyacá, Colombia, were studied essentially with Mössbauer spectroscopy. The samples were treated with NaOH 5 mol L^???1 in order to increase the proportion of iron oxides, by selectively dissolving silicate minerals and any remaining gibbsite, before the physical analysis. Room temperature Mössbauer data revealed that all samples do contain major proportions (>50 % of the relative subspectral area) of hematite along with (super) paramagnetic species as iron-bearing chemical compounds. The superparamagnetic contribution may be due to very fine grains of iron oxides, including nanometric hematite.     

FC-空间中新的连续选择定理及其对广义模糊约束多目标对策的应用

建立了非紧FC-空间中新的连续选择定理,作为应用,获得了非紧FC-空间中广义模糊约束多目标对策的弱Pareto平衡存在定理.我们的结论统一、改进和推广了一些近期文献的已知结果.     

g factor of hydrogenlike ²⁸Si¹³⁺

We determined the experimental value of the g factor of the electron bound in hydrogenlike 2?Si13? by using a single ion confined in a cylindrical Penning trap. From the ratio of the ion's cyclotron frequency and the induced spin flip frequency, we obtain g = 1.995 348 958 7(5)(3)(8). It is in excellent agreement with the state-of-the-art theoretical value of 1.995 348 958 0(17), which includes QED contributions up to the two-loop level of the order of (Zα)2 and (Zα)? and represents a stringent test of bound-state quantum electrodynamics calculations.     

Towards minimization of chlorinated solvents consume in Fourier transform infrared spectroscopy determination of Propamocarb in pesticide formulations

A method has been developed for Fourier transform infrared (FTIR) spectroscopy determination of Propamocarb in emulsifiable pesticide concentrate formulations. Five microliter sample was directly injected without any pretreatment in a CHCl3 stream at 2 mL min(-1) into a closed system and the FTIR spectra of sample and standard solutions were obtained using a nominal resolution of 4 cm(-1) from 4000 to 900 cm(-1) spectral region and accumulating 2 scans per spectrum. Propamocarb determination was based on the measurement of flow injection analysis (FIA) recording height established from FTIR peak area measurements from 1713 to 1703 cm(-1) corrected using a baseline defined at 2000 cm(-1). The concentration of Propamocarb in samples was calculated by interpolation in an external calibration line obtained from several injections of 2 microL of a 47% (w/v) standard solution into the CHCl3 closed system. This procedure provided a limit of detection of 0.8% (w/v) in the original sample, a sensitivity of 0.3190 absorbance units mL mg(-1) for a path length of 0.11 mm and a relative standard deviation of 0.2% for five independent measurements at 0.74 mg mL(-1) concentration level. The maximum sampling frequency of the whole procedure was 34 h(-1) and the waste generation was reduced to only 2 mL of CHCl3 solution per sample and additional 2 mL for the whole calibration line.     

On-line gel permeation chromatography-attenuated total reflectance-Fourier transform infrared determination of lecithin and soybean oil in dietary supplements

Gel permeation chromatography (GPC) with attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectrometry detection has been proposed for the simultaneous determination of lecithin and soybean oil in dietary supplements. The method involves the extraction of analytes with dichloromethane in an ultrasound water bath and the injection of 2 ml of centrifuged and filtered extracts into the system integrated by two Envirogel GPC columns (19 mm x150 mm, 19 mm x 300 mm) coupled on-line. Dichloromethane was used as mobile phase. A method has been developed to select the most appropriated wavenumber to be used for the determination of each considered compound from the calculation of a factor which maximizes the analyte signal minimizing the interferent contributions, being selected the detection wavenumbers of 1034 and 1138 cm(-1) for lecithin and soybean oil, respectively in the first order derivative ATR-FTIR spectra. The method provides limits of detection of 2 and 4 mg ml(-1) for lecithin and soybean oil and repeatability values, measured as relative standard deviation, of 2.5% and 3.4% being extended the linear range till 100 mg ml(-1) for lecithin and up to 50 mg ml(-1) for soybean oil. Accurate results were found for 10 synthetic samples and 7 commercial dietary supplement preparations.     

Univariate method for background correction in liquid chromatography-Fourier transform infrared spectrometry

An univariate method is proposed for background correction in on-line gradient liquid chromatography-Fourier transform infrared (LC-FTIR) spectrometry using acetonitrile:water as mobile phase components. The method is based on the calculation of the ratio of absorbances (AR) at two characteristic wavenumbers for each spectrum. This parameter is subsequently used to locate the most appropriated eluent spectrum within a reference spectra matrix (RSM) to be subtracted from each spectrum included in the sample chromatogram. To correct minor changes in eluent spectra intensity during the elution of analytes, a correction factor (Kf), defined as the ratio of the absorbance of the sample and the selected eluent spectrum at a defined wavenumber was determined. The performance of the procedure was evaluated by correcting an on-line gradient LC-FTIR injection of a mixture of two pesticides (Atrazine and Diuron). Using the AR of the absorbance at 2248.6 and 2256.3 cm(-1) and a Kf at 2248.6 cm(-1), the correlation factors between FTIR spectra extracted at the peak apex from the LC-FTIR chromatogram and those obtained from pure pesticide standards were 0.975 and 0.94 for Atrazine and Diuron, respectively.     

Phytochemical characterisation of Phlomis linearis Boiss. & Bal and screening for anticholinesterase,antiamylase, antimicrobial,and cytotoxic properties

In the present work, essential oil and fatty acids and extracts obtained from aerial parts of Phlomis linearis Boiss. & Bal. were investigated for chemical composition and biological activities. The phytochemical analyses were conducted with gas chromatography-mass spectrometry/flame ionisation detector (GC-MS/FID) and liquid chromatography-mass spectromtetry (LC-MS/MS) techniques. The extracts and essential oil were studied for α-amylase and acetylcholinesterase activities with two different spectrophotometric methods. Antimicrobial activities of the extracts were investigated by microdilution. The extracts were evaluated in vitro for cytotoxic effects against cancer and normal cell lines by MTT assay. The essential oil (EO) contained α-pinene (12.5%) and β-caryophyllene (10.7%) as main compounds. Palmitic (26.5%) and nonadecanoic acids (26.6%) were determined as fatty acids. Phytochemical analysis of the extracts found phenolic acids, phlinosides, verbascoside, and flavonoids. The extracts and essential oil demonstrated poor α-amylase inhibitory activity. The best acetylcholinesterase inhibitory activity was obtained for diethly ether extract of P. linearis (67.2 ± 3.4%) at 10 mg /mL concentration. Ethyl acetate extract found to be effective against Staphlococcus aureus at a minimum inhibitory concentration (MIC) of 156.26 µg/mL. Diethyl ether extract of P. linearis was active on A549 cell lines with an IC₅₀ = 316 ± 4.16 µg/mL when compared with cisplatin IC₅₀ = 24.43 ± 0.14 µg/mL. To the best of our knowledge, the present work is the first comprehensive report on anti-acetylcholinesterase, anti-α-amylase, and antimicrobial activities, as well as cytotoxic effects of P. linearis.