Topic
Calibration curve
About: Calibration curve is a research topic. Over the lifetime, 6552 publications have been published within this topic receiving 95128 citations.
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TL;DR: In this paper, the effect of the sample matrix on lead emission intensity was studied by means of collinear double pulse (DP)-laser induced breakdown spectroscopy (LIBS).
43 citations
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TL;DR: Current instrumentation is capable of measuring the highest dissolved gas concentration observed in end-member hydrothermal fluids, and the calibration curves relating band height ratios to gas concentration are linear and valid for a range of temperatures, pressures, and salinities.
Abstract: Laboratory experiments have been performed using laser Raman spectroscopy to analyze carbon dioxide (CO2) and methane (CH4) dissolved in water and seawater. Dissolved CO2 is characterized by bands at ∼1275 and 1382 Δcm−1. Dissolved CH4 is characterized by a dominant band at ∼2911 Δcm−1. The laboratory instrumentation used for this work is equivalent to the sea-going Raman instrument, DORISS (Deep Ocean Raman In Situ Spectrometer). Limits of quantification and calibration curves were determined for each species. The limits of quantification are ∼10 mM for CO2 and ∼4 mM for CH4. A ratio technique is used to obtain quantitative information from Raman spectra: the gas bands are referenced to the O–H stretching band of water. The calibration curves relating band height ratios to gas concentration are linear and valid for a range of temperatures, pressures, and salinities. Current instrumentation is capable of measuring the highest dissolved gas concentration observed in end-member hydrothermal fluids. Further development work is needed to improve sensitivity and optimize operational configurations.
43 citations
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TL;DR: In this paper, a procedure for the determination of morphine in non-aqueous, water immiscible, process streams by sequential injection analysis is presented, based upon the chemiluminescence reaction of morphine with acidic potassium permanganate in the presence of sodium polyphosphate, which was carried out in a heterogeneous reaction environment.
Abstract: A procedure for the determination of morphine in non-aqueous, water immiscible, process streams by sequential injection analysis is presented. Detection was based upon the chemiluminescence reaction of morphine with acidic potassium permanganate in the presence of sodium polyphosphate, which was carried out in a heterogeneous reaction environment. The calibration graph (range 0.005–0.12% m/v) was non-linear, with a polynomial equation of best fit of y = –384x2 + 139x – 4.84 (R2 = 0.9990), where y represents the singal (mV) and x represents the morphine concentration (% m/v), and was analytically useful over the range 0.01–0.1% m/v. Precision (as measured by relative standard deviation) was 6.0% for 10 replicate analyses of a non-aqueous morphine standard (0.075% m/v).Methyltriphenylphosphonium permanganate was investigated as an alternative chemiluminescent reagent and was found to deliver a similar analytical performance to potassium permanganate. Sequential injection analysis coupled with chemiluminescence detection afforded results for the determination of morphine in non-aqueous process samples which were in good agreement with those obtained using a standard liquid chromatographic method, with an analytical throughput in excess of 120 h–1.
42 citations
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TL;DR: The proposed technique allows a rapid, simple, sensitive and selective analysis of trace mercury(II) in water samples by monitoring the color change of a microfluidic Paper-based Analytical Device.
42 citations
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TL;DR: An on-line automated flow injection system with microwave-assisted sample digestion for the electrothermal atomic absorption spectrometric determination of bismuth in biological materials is described.
42 citations