Determination of trace concentrations of copper by FIA-FAAS after preconcentration on chelating sorbents

1989 ◽  
Vol 54 (7) ◽  
pp. 1785-1794 ◽  
Author(s):  
Vlastimil Kubáň ◽  
Josef Komárek ◽  
Zbyněk Zdráhal
Keyword(s):  
Sampling Frequency ◽  
Copper Determination ◽  
Flow Rates ◽  
Sample Injection ◽  
Injection Flow ◽  
Chelating Sorbents ◽  
Set Up ◽  
Trace Concentrations ◽  
Better Than

A FIA-FAAS apparatus containing a six-channel sorption equipment with five 3 x 26 mm microcolumns packed with Spheron Oxin 1 000, Ostsorb Oxin and Ostsorb DTTA was set up. Combined with sorption from 0.002M acetate buffer at pH 4.2 and desorption with 2M-HCl, copper can be determined at concentrations up to 100, 150 and 200 μg l-1, respectively. For sample and eluent flow rates of 5.0 and 4.0 ml min-1, respectively, and a sample injection time of 5 min, the limit of copper determination is LQ = 0.3 μg l-1, repeatability sr is better than 2% and recovery is R = 100 ± 2%. The enrichment factor is on the order of 102 and is a linear function of time (volume) of sample injection up to 5 min and of the sample injection flow rate up to 11 ml min-1 for Spheron Oxin 1 000 and Ostsorb DTTA. For times of sorption of 60 and 300 s, the sampling frequency is 70 and 35 samples/h, respectively. The parameters of the FIA-FAAS determination (acetylene-air flame) are comparable to or better than those achieved by ETA AAS. The method was applied to the determination of traces of copper in high-purity water.

Time and Latitude in South Africa

1972 ◽  
Vol 1 ◽  
pp. 27-38
Author(s):  
J. Hers
Keyword(s):  
South Africa ◽  
Cape Town ◽  
Astronomical Observations ◽  
Royal Observatory ◽  
The Republic ◽  
Astronomical Determination ◽  
Limited Accuracy ◽  
Better Than

In South Africa the modern outlook towards time may be said to have started in 1948. Both the two major observatories, The Royal Observatory in Cape Town and the Union Observatory (now known as the Republic Observatory) in Johannesburg had, of course, been involved in the astronomical determination of time almost from their inception, and the Johannesburg Observatory has been responsible for the official time of South Africa since 1908. However the pendulum clocks then in use could not be relied on to provide an accuracy better than about 1/10 second, which was of the same order as that of the astronomical observations. It is doubtful if much use was made of even this limited accuracy outside the two observatories, and although there may – occasionally have been a demand for more accurate time, it was certainly not voiced.

Respirometry for determination of the influents SS-concentration

1996 ◽  
Vol 33 (1) ◽  
pp. 311-323 ◽  
Author(s):  
A. Witteborg ◽  
A. van der Last ◽  
R. Hamming ◽  
I. Hemmers
Keyword(s):  
Experimental Design ◽  
Activated Sludge ◽  
Substrate Concentration ◽  
Full Scale ◽  
Activated Sludge Process ◽  
Respiration Rates ◽  
On Line ◽  
Large Measurement ◽  
Set Up

A method is presented for determining influent readily biodegradable substrate concentration (SS). The method is based on three different respiration rates, which can be measured with a continuous respiration meter which is operated in a cyclic way. Within the respiration meter nitrification is inhibited through the addition of ATU. Simulations were used to develop the respirometry set-up and decide upon the experimental design. The method was tested as part of a large measurement programme executed at a full-scale plant. The proposed respirometry set-up has been shown to be suitable for a semi-on-line determination of an influent SS which is fully based on the IAWQ #1 vision of the activated sludge process. The YH and the KS play a major role in the principle, and should be measured directly from the process.

Determination of specific interfacial areas in swirled two-phase flow

1983 ◽  
Vol 48 (3) ◽  
pp. 842-853
Author(s):  
Kurt Winkler ◽  
František Kaštánek ◽  
Jan Kratochvíl
Keyword(s):  
Interfacial Area ◽  
Liquid Volume ◽  
Upward Flow ◽  
Two Phase ◽  
Flow Rates ◽  
Mist Flow ◽  
Interfacial Areas ◽  
Correlation Parameters ◽  
Flow Components

Specific gas-liquid interfacial area in flow tubes 70 mm in diameter of the length 725 and 1 450 mm resp. containing various swirl bodies were measured for concurrent upward flow in the ranges of average gas (air) velocities 11 to 35 ms-1 and liquid flow rates 13 to 80 m3 m-2 h-1 using the method of CO2 absorption into NaOH solutions. Two different flow regimes were observed: slug flow swirled annular-mist flow. In the latter case the determination was carried out separately for the film and spray flow components, respectively. The obtained specific areas range between 500 to 20 000 m3 m-2. Correlation parameters are energy dissipation criteria, related to the geometrical reactor volume and to the static liquid volume in the reactor.

Laser optoacoustic detection of trace concentration levels of ethylene, vinylchloride, and styrene in the atmosphere

1989 ◽  
Vol 54 (10) ◽  
pp. 2667-2673 ◽  
Author(s):  
Vojtěch Steiner ◽  
Pavel Engst ◽  
Zdeněk Zelinger ◽  
Milan Horák
Keyword(s):  
Detection Limit ◽  
Emission Line ◽  
Laser Line ◽  
Laser Source ◽  
Trace Concentration ◽  
Selective Determination ◽  
Hygienic Standard ◽  
Trace Concentrations ◽  
Concentration Levels

The optoacoustic analyzer with a tunable CO2 laser source employed in the present work permits a selective determination of ethylene in trace concentrations higher than 5 ppb (=detection limit for the 10P(14) emission line of the CO2 laser, ν = 949.5 cm-1) and of vinylchloride higher than 42 ppb (= detection limit for the 10P(22) CO2 laser line, ν= 942.4 cm-1). this method covers for both compounds the concentration range corresponding to the hygienic standard. It can be also used for the determination of styrene vapour with concentrations higher than 1.5 ppm.

Extra-Column Effects in Determination of Rate Parameters by the Chromatographic Method

1996 ◽  
Vol 61 (6) ◽  
pp. 844-855 ◽  
Author(s):  
Olga Šolcová ◽  
Petr Schneider
Keyword(s):  
Chromatographic Method ◽  
Dynamic Method ◽  
Axial Dispersion ◽  
Transport Parameters ◽  
Porous Particles ◽  
Loop Detector ◽  
Single Pellet ◽  
Set Up ◽  
Extra Column Effects

It was shown that the sampling loop, detector and connecting elements in the chromatographic set-up for determination of transport parameters by the dynamic method significantly influence the response peaks from columns packed with porous or nonporous particles. A method, based on the use of convolution theorem, was developed which can take these effects into account. The applicability of this method was demonstrated on the case of axial dispersion in a single-pellet-string column (SPSR) packed with nonporous particles. It is possible to handle also responses from columns packed with porous particles by a similar procedure.

scholarly journals Measuring the quartic Higgs self-coupling at a multi-TeV muon collider

2020 ◽  
Vol 2020 (9) ◽  
Author(s):  
M. Chiesa ◽  
F. Maltoni ◽  
L. Mantani ◽  
B. Mele ◽  
F. Piccinini ◽  
...  
Keyword(s):  
Higgs Boson ◽  
Center Of Mass ◽  
Mass Energy ◽  
Simple Analysis ◽  
Proton Proton ◽  
Coupling Interaction ◽  
Center Of Mass Energy ◽  
Muon Collider ◽  
Better Than

Abstract Measuring the shape of the Higgs boson potential is of paramount importance, and will be a challenging task at current as well as future colliders. While the expectations for the measurement of the trilinear Higgs self-coupling are rather promising, an accurate measurement of the quartic self-coupling interaction is presently considered extremely challenging even at a future 100 TeV proton-proton collider. In this work we explore the sensitivity that a muon collider with a center of mass energy in the multi-TeV range and luminosities of the order of 1035cm−2s−1, as presently under discussion, might provide, thanks to a rather large three Higgs-boson production and to a limited background. By performing a first and simple analysis, we find a clear indication that a muon collider could provide a determination of the quartic Higgs self-coupling that is significantly better than what is currently considered attainable at other future colliders.

scholarly journals Comparison of different models to calculate the viscosity of biogas and biomethane in order to accurately measure flow rates for conformity assessment

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Karine Arrhenius ◽  
Oliver Büker
Keyword(s):  
Binary Mixtures ◽  
Flow Rate ◽  
Correction Method ◽  
Gas Mixtures ◽  
Conformity Assessment ◽  
Flow Rates ◽  
Unknown Composition

AbstractThe study presents an optimised method to correct flow rates measured with a LFE flowmeter pre-set on methane while used for gas mixtures of unknown composition at the time of the measurement. The method requires the correction of the flow rate using a factor based on the viscosity of the gas mixtures once the composition is accurately known. The method has several different possible applications inclusive for the sampling of biogas and biomethane onto sorbent tubes for conformity assessment for the determination of siloxanes, terpenes and VOC in general. Five models for the calculation of the viscosity of the gas mixtures were compared and the models were used for ten binary mixtures and four multi-component mixtures. The results of the evaluation of the different models showed that the correction method using the viscosity of the mixtures calculated with the model of Reichenberg and Carr showed the smallest biases for binary mixtures. For multi-component mixtures, the best results were obtained when using the models of Lucas and Carr.

scholarly journals Performance of the SoLid reactor neutrino detector

2019 ◽  
Vol 219 ◽  
pp. 08003
Author(s):  
Maja Verstraeten
Keyword(s):  
Quality Control ◽  
Energy Resolution ◽  
Neutrino Detector ◽  
Channel Response ◽  
In Situ Calibration ◽  
Reactor Neutrino ◽  
Li Isotope ◽  
Better Than

The SoLid Collaboration is currently operating a 1.6 ton neutrino detector near the Belgian BR2 reactor. Its main goal is the observation of the oscillation of electron antineutrinos to previously undetected flavour states. The highly segmented SoLid detector employs a compound scintillation technology based on PVT scintillator in combination with LiF-ZnS(Ag) screens containing the 6Li isotope. The experiment has demonstrated a channel-to-channel response that can be controlled to the level of a few percent, an energy resolution of better than 14% at 1 MeV, and a determination of the interaction vertex with a precision of 5 cm. This contribution highlights the major outcomes of the R&D program, the quality control during component manufacture and integration, the current performance and stability of the full-scale system, as well as the in-situ calibration of the detector with various radioactive sources.

scholarly journals An evaluation of the Kemtek 1000 sample processor

1988 ◽  
Vol 10 (1) ◽  
pp. 37-42 ◽  
Author(s):  
M. J. Wheeler ◽  
Linzi Waiters
Keyword(s):  
Probe System ◽  
Carry Over ◽  
Set Up ◽  
Accuracy Speed ◽  
Better Than ◽  
The Way

The Kemtek 1000 Sample Processor has been evaluated for precision, accuracy, speed and reliability. Precision was better than 1.0% at all volumes tested and accuracy within ±5%. A l00-tube assay could be set up within 15 min when patient specimens plus two reagents were sampled using a two probe system. Carry-over could be reduced to <0.01% by using a sufficient number of wash steps, the latter being related to the assay requirements. Evidence was found for adsorption of protein to the probe tubing but inaccuracies due to this could be reduced by introducing wash steps between samples. Problems over 12 months have been minor and quickly resolved. The authors were pleased with the way the processor performed and their staffhave confidence in leaving it to set up their assays.

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