Academic literature on the topic 'Absorbance interference study'
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Journal articles on the topic "Absorbance interference study"
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Ding, Tao, Lianbai Gu, and Xiang Liu. "Simultaneous determination of chlorine dioxide and hypochlorous acid in bleaching system." BioResources 6, no. 2 (2011): 1868–79. http://dx.doi.org/10.15376/biores.6.2.1868-1879.
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This study has demonstrated a rapid spectroscopic method for the determination of chlorine dioxide and hypochlorous acid concentrations in the pulp bleaching processes. It was found that chlorine dioxide and hypochlorous acid have an isosbestic wavelength of 295 nm. The soluble lignin in such a system is the main interference, but can be corrected by determining the absorbances at 295 nm, 380 nm, and 480 nm. Thus, based on the spectroscopic measurements at 295 nm (the isosbestic point wavelength for chlorine dioxide and hypochlorous acid), 380 nm (absorbance wavelength of chlorine dioxide) and 480 nm (the acid soluble lignin absorbance wavelength), the chlorine dioxide and hypochlorous acid concentrations in the bleaching process can be quantified. However, hypochlorous acid was not detected in the real bleaching effluent for its low content. The present method is simple, rapid, accurate, and has the potential for on-line monitoring of the chlorine dioxide bleaching process.
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Yudistira, Hadi Teguh, and Kiki Kananda. "The Preliminary Microwave Metamaterial Absorber Based on Ring-Shaped for Stealth Technology." IOP Conference Series: Earth and Environmental Science 1209, no. 1 (2023): 012028. http://dx.doi.org/10.1088/1755-1315/1209/1/012028.
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Abstract Controlling electromagnetic waves on the material is needed by several applications such as sensors, stealth technology, and energy harvesting. An artificial material that could control electromagnetic waves is called metamaterial. Meanwhile, a metamaterial absorber can absorb the electromagnetic wave. Two concepts can be used to explain the absorbing phenomena on metamaterial absorber: the matching impedance of the air and the part of the imaginary that is high of the index of refractive collectively or the theory of interference that is destructive. The correlation of matching air impedance with destructive interference theory has been found by Yudistira in his previous works. In this study, the preliminary research of metamaterial absorbers based on ring shape is presented. The 40 mm, 35 mm, 30 mm, and 25 mm ring-shaped widths are applied to this work. We used numerical simulation work to understand the performance of metamaterial absorbers based on ring-shaped. CST microwave studio was used for numerical simulation work. The absorbance peak results for w=20, w=17.5, w=15, and w=12.5 mm are 0.92 at 3.43 GHz, 0.95 at 3.7 GHz, 0.95 at 4.04 GHz and 0.99 at 4.47 GHz, severally. The maximum absorbance is yielded to 0.99 absorbances for 25 mm of the width of the ring-shaped.
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Monteiro-Silva, Jorge, and Martins. "Optical Sensing of Nitrogen, Phosphorus and Potassium: A Spectrophotometrical Approach Toward Smart Nutrient Deployment." Chemosensors 7, no. 4 (2019): 51. http://dx.doi.org/10.3390/chemosensors7040051.
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The feasibility of a compact, modular sensing system able to quantify the presence of nitrogen, phosphorus and potassium (NPK) in nutrient-containing fertilizer water was investigated. Direct UV-Vis spectroscopy combined with optical fibers were employed to design modular compact sensing systems able to record absorption spectra of nutrient solutions resulting from local producer samples. N, P, and K spectral interference was studied by mixtures of commercial fertilizer solutions to simulate real conditions in hydroponic productions. This study demonstrates that the use of bands for the quantification of nitrogen with linear or logarithmic regression models does not produce analytical grade calibrations. Furthermore, multivariate regression models, i.e., Partial Least Squares (PLS), which consider specimens interference, perform poorly for low absorbance nutrients. The high interference present in the spectra has proven to be solved by an innovative self-learning artificial intelligence algorithm that is able to find interference modes among a spectral database to produce consistent predictions. By correctly modeling the existing interferences, analytical grade quantification of N, P, and K has proven feasible. The results of this work open the possibility of real-time NPK monitoring in Micro-Irrigation Systems.
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Levitt, Stephen R. "Spectrophotometric Measurement of Lithium in Human Saliva Using the Chromogenic Reagent Thorin." Acta Chimica Slovenica 70, no. 3 (2023): 430–39. http://dx.doi.org/10.17344/acsi.2023.8121.
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The feasibility of using the chromogenic dye Thorin to spectrophotometrically measure lithium concentration in human saliva was explored. Absorbance wavelength maximum of the Li-Thorin complex was found to be 480 nm. Absorbance at 480 nm was obtained for saliva calibration standards containing 0.00–5.29 mEq/L of lithium. A least-squares fit produced a regression equation y = 0.128x + 1.449, R = 0.997. This was used to predict lithium concentrations in both artificially prepared lithium/saliva test solutions and in hospitalized patients treated with lithium. Results agree well with atomic absorption spectroscopy. Using a reagent blank with an equivalent amount of saliva as the test samples eliminated protein and electrolyte absorbance interference. This study supports the continued exploration of this method as a non-invasive point-of-care testing approach for monitoring saliva lithium in bipolar disorder.
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Jhanwar, Bharat, Bhupendra Singh, Geetanjali Saini, and Surajpal Verma. "METHOD DEVELOPMENT AND VALIDATION FOR SIMULTANEOUS ESTIMATION OF LEVOSULPIRIDE AND RABEPRAZOLE SODIUM: A NEW ANALYTICAL Q-ABSORBANCE RATIO APPROACH." Asian Journal of Pharmaceutical and Clinical Research 10, no. 16 (2017): 22. http://dx.doi.org/10.22159/ajpcr.2017.v10s4.21331.
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Objective: The aim of the study was to develop a precise, accurate, and rapid ultraviolet spectrophotometric method for simultaneous estimation of levosulpiride (LEVO) and rabeprazole sodium (RBS) in the binary mixture and to validate the method as per ICH guidelines.Method: Estimation of LEVO and RBS was performed by Q-absorbance method. Analysis was performed using the ratio of absorbance at two selected wavelengths, one at iso-absorptive point and other is the absorbance maxima of any one of the components. Single scan spectrum and the overlain spectrum conclude that absorbance maxima of LEVO and RBS are 228 and 291.8 nm, respectively, with a coinciding iso-absorptive point at 255 nm. Method uses a ratio of absorbance for assay at 255 and the second wavelength is 291.8 nm, λmax for RBS. It is also applicable at 228 nm, as the second wavelength.Results: Linearity of LEVO and RBS was found to be 25-125 and 4-36 μg/ml, respectively. The accuracy of the LEVO and RBS was found 99.26% and 99.51%, respectively and Sandell’s sensitivity ranged between 0.0238 and 0.594 μg/cm2. Assay of LEVO (75 mg) and RBS (20 mg) in capsule dosage form was found 99.5% and 98.69% w/w, respectively.Conclusions: The developed method for the estimation of LEVO and RBS in binary mixture were found to be simple, accurate, robust, and reproducible. No interference of excipients and the degraded product was found during the estimation. Therefore, the method can be successfully applied for routine quality control analysis.RBS) in the binary mixture and to validate the method as per ICH guidelines.Method: Estimation of LEVO and RBS was performed by Q-absorbance method. Analysis was performed using the ratio of absorbance at two selected wavelengths, one at iso-absorptive point and other is the absorbance maxima of any one of the components. Single scan spectrum and the overlain spectrum conclude that absorbance maxima of LEVO and RBS are 228 and 291.8 nm respectively with a coinciding iso-absorptive point at 255 nm. Method uses ratio of absorbance for assay at 255 and the second wavelength is 291.8 nm, λmax for RBS. It is also applicable at 228 nm, as the second wavelength.Results: Linearity of LEVO and RBS were found to be 25-125and 4-36 μg/ml respectively. Accuracy of the LEVO and RBS was found 99.26 and 99.51% respectively and Sandell’s sensitivity ranged between 0.0238 and 0.594 𝜇g/cm2. Assay of LEVO (75 mg) and RBS (20 mg) in capsule dosage form was found 99.5 and 98.69% w/w respectively.Conclusions: The developed method for the estimation of LEVO and RBS in binary mixture were found to be simple, accurate, robust and reproducible. No interference of excipients and the degraded product were found during the estimation. Therefore the method can be successfully applied for routine quality control analysis.
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Lawal, Babatunde AS, and Finian K. Odoala. "Interference in drug assay by phytochemicals: An experience with colorimetric assay of amlodipine in physiological fluids." Tropical Journal of Pharmaceutical Research 22, no. 11 (2024): 2327–32. http://dx.doi.org/10.4314/tjpr.v22i11.12.
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Purpose: To investigate the potential interactions between methanol extract of Aframomum melegueta seeds (AMSE) and amlodipine (AML).
 Methods: Amlodipine concentrations 2.5, 5.0, 7.5, 10, 12.5 and 15 µg/mL were assayed in vitro with or without AMSE using potassium ferricyanide/FeCl3 (FeCl3/K4(Fe(CN)6)) method. The resulting solution was wavelength-scanned in the range 380 – 950 nm and absorbance read at 393.1, 455.6 and 774.8 nm.
 Results: Aframomum melegueta seeds (AMSE), when present in biological fluids and solutions of AML, interfered significantly with FeCl3/K4(Fe(CN))6. The highest interference occurred at 774.8 nm, and 50 µg/mL AMSE gave as much as 1.5 absolute unit increase in absorbance of 2.5 µg/mL when compared to its absence. Spectral scan of the sample revealed two additional peaks at 393.1 and 455.6 nm with only 0.07 and 0.16 nm unit increases in the presence of AMSE. Concentration–absorbance relationship at these two wavelengths satisfied Beer-Lambert’s law. Beyond 15 µg/mL AML at 774.8 nm, Beer-Lambert’s law was not followed.
 Conclusion: This study highlights the potential interactions between components of the methanol extract of Aframomum melegueta seeds on assay methods of AML. Furthermore, reliable concentration measurements have been made at 393.1 or 455.6 nm. This should be kept in mind when carrying out drug measurements in populations where concurrent use of herbal remedies is highly probable.
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Pons, Joan Farré, Alba Alumá, Felipe Antoja, Carmen Biosca, María-Jesús Alsina, and Román Galimany. "Evaluation of the Dacos 3.0 analyser." Journal of Automatic Chemistry 12, no. 4 (1990): 153–62. http://dx.doi.org/10.1155/s1463924690000207.
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The selective multitest Coulter Dacos 3.0 analyser was evaluated according to the guidelines of the Comisión de Instrumentación de la Sociedad Española de Química Clínica and of the European Committee for Clinical Laboratory Standards.The evaluation was performed in four steps: examination of the analytical units; evaluation of routine working; study of interferences; and assessment of practicability.The evaluation included a photometric study. The inaccuracy is acceptable for 340 nm and 420 nm, and the imprecision at absorbances from 0.05 to 2.00 ranged from 0.06 to 0.28% at 340 nm and from 0.06 to 0.08% at 420 nm. The linearity showed some dispersion at low absorbance for PNP at 420 nm and the drift was negligible.The imprecision of the pipette delivery system, the temperature control system and the washing system were satisfactory.In routine work conditions, seven analytical methods were studied: glucose, creatinine, iron, total protein, AST, ALP and calcium. Within-run imprecision ranged, at low concentrations, from 0.9% (CV) for glucose, to 7.6% (CV) for iron; at medium concentrations, from 0.7% (CV) for total protein to 5.2% (CV) to creatinine; and at high concentrations, it ranged from 0.6% (CV) for glucose to 3.9% (CV) for ALP.Between-run imprecision at low concentrations ranged from 1.4% (CV) for glucose to 15.1% (CV) for iron; at medium concentrations it ranged from 1.2% (CV) for protein to 6.7% (CV) for iron; and at high concentrations the range is from l.2for AST to 5.7% (CV) for iron.No contamination was found in the sample carry-over study. Some contamination was found in the reagent carry-over study (total protein due to iron and calcium reagents). Relative inaccuracy is good for all the constituents assayed. Only LDH (high and low levels) and urate (low level) showed weak and negative interference caused by turbidity, and γ-GT (high level) and amylase, bilirubin and ALP (two levels) showed a negative interference caused by haemolysis.
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Jiang, Fengcheng, Yao Qiu, Mingshi Wang, et al. "Interference and Elimination of Fe3+ During Spectrophotometric Testing of Typical Pollutants in Coking Wastewater." International Journal of Natural Resources and Environmental Studies 2, no. 2 (2024): 63–69. http://dx.doi.org/10.62051/ijnres.v2n2.07.
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As typical pollutants in coking wastewater, pyridine, indole, quinoline, and phenol have the advantages of rapidity and accuracy when determined in aqueous solution using UV spectrophotometry, but the presence of other substances in the water can interfere with the results. In this study, the spectrophotometric detection of pyridine, indole, quinoline, and phenol in coking wastewater was interfered with by Fe3+. To minimize this interference, hydroxylamine hydrochloride (HA) was selected as a masking agent to eliminate the interference of Fe3+ on the detection. The results indicated that spectrophotometric determination was significantly affected by Fe3+, and the level of interference increased with the concentration of Fe3+. HA can effectively reduce the absorbance of Fe3+ in the wavelength range of 250-350 nm. It exhibits a strong masking effect on the determination of Fe3+ in indole and phenol solutions, but it hampers the detection of pyridine and quinoline. HA has a better elimination effect on the interference of different concentrations of Fe3+, which can make the relative error of the determination results of indole and phenol less than 5% and 10%, respectively.
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Andraos, Charlene, Il Je Yu, and Mary Gulumian. "Interference: A Much-Neglected Aspect in High-Throughput Screening of Nanoparticles." International Journal of Toxicology 39, no. 5 (2020): 397–421. http://dx.doi.org/10.1177/1091581820938335.
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Despite several studies addressing nanoparticle (NP) interference with conventional toxicity assay systems, it appears that researchers still rely heavily on these assays, particularly for high-throughput screening (HTS) applications in order to generate “big” data for predictive toxicity approaches. Moreover, researchers often overlook investigating the different types of interference mechanisms as the type is evidently dependent on the type of assay system implemented. The approaches implemented in the literature appear to be not adequate as it often addresses only one type of interference mechanism with the exclusion of others. For example, interference of NPs that have entered cells would require intracellular assessment of their interference with fluorescent dyes, which has so far been neglected. The present study investigated the mechanisms of interference of gold NPs and silver NPs in assay systems implemented in HTS including optical interference as well as adsorption or catalysis. The conventional assays selected cover all optical read-out systems, that is, absorbance (XTT toxicity assay), fluorescence (CytoTox-ONE Homogeneous membrane integrity assay), and luminescence (CellTiter Glo luminescent assay). Furthermore, this study demonstrated NP quenching of fluorescent dyes also used in HTS (2′,7′-dichlorofluorescein, propidium iodide, and 5,5′,6,6′-tetrachloro-1,1′,3,3′-tetraethyl-benzamidazolocarbocyanin iodide). To conclude, NP interference is, as such, not a novel concept, however, ignoring this aspect in HTS may jeopardize attempts in predictive toxicology. It should be mandatory to report the assessment of all mechanisms of interference within HTS, as well as to confirm results with label-free methodologies to ensure reliable big data generation for predictive toxicology.
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Saputro, Sulistyo, Ngatidjo Hadipranoto, and Agus Kuncaka. "Study on the Interference of Iron, Aluminium and Silicon on the Atomic Absorption Spectrometric Determination of Mangan in Laterite Mineral." Indonesian Journal of Chemistry 1, no. 2 (2010): 98–104. http://dx.doi.org/10.22146/ijc.21950.
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Interference of iron, aluminum and silicon on the determination of mangan in laterite mineral by atomic absorption spectrometry has been investigated. Dissolution of laterite mineral into solution have been carried out by wet method destruction using combination of 7 mL of aquaregia, 7.5 mL of concentrated perchloric acid and 9 mL of fluoride acid 48% In sealed teflon flask heated at temperature of about 110 °C for 3 hours to determine the content of Mn element in laterite mineral directly. Interference of these three metals were carried out by evaluating the differences of Mn absorbance at wavelength 279.50 nm and slit width 0.2 nm between the solutions containing mangan only and those containing the some amount of mangan together with the interfering elements at those concentration range in laterite mineral. The result showed that both iron at concentration of 100 ppm until 500 ppm and aluminum at concentration at 3 ppm until 15 ppm caused significant and non-linear interference on the determination of Mn 2 ppm. Interference of iron was effectively eliminated by releasing action of aluminum. The signal depression reductional decrease due to 234 ppm of silicon on the determination of Mn 2 ppm can be eliminated by adding 2.30 mL of CaCl2 0.2% (m/v) into these solution. The content of Mn in the laterite mineral after and before adding of CaCl2 into solution were 2407.04 ± 59.26 μg g-1 and 2311.76 ± 23.61 μg g-1, respectively. This result was significantly different at confidence level 95% as shown by the value of tcalculated=4.91 that was higher than ttable=4.30.
Book chapters on the topic "Absorbance interference study"
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Jordan, Robert B. "Experimental Methods." In Reaction Mechanisms of Inorganic and Organometallic Systems. Oxford University Press, 2007. http://dx.doi.org/10.1093/oso/9780195301007.003.0012.
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A kinetic study generally proceeds after the reactants, products and stoichiometry of the reaction have been satisfactorily characterized. The more one knows about the chemistry of the reaction, the better the conclusions that one can draw from a kinetic study. The discussion here describes techniques often used in inorganic studies, emphasizes their time range and general area of applicability and gives some examples of their use. Further details can be found in other sources. Any experimental kinetic method must somehow monitor change of concentration with time. Many studies are done under pseudo-first-order conditions, and then one must monitor the deficient reactant or product(s) because the other species undergo small changes in concentration. The kinetic method(s) of choice often will be dictated by the time scale of the reaction. The detection method(s) will be determined by the spectroscopic properties of the species to be monitored. The efficient use of materials can be a significant factor in the choice of method because a kinetic study generally involves a number of runs at different concentrations and temperatures, and conservation of difficult to prepare or expensive reagents may be a critical factor. The detection method should be as species specific as possible, and ideally one would like to measure both reactant disappearance and product formation. The method must not be subject to interference from other reactants and should be applicable under a wide range of concentration conditions so that the rate law can be fully explored. Often there is a practical trade-off between specificity, sensitivity and reaction time. For example, NMR is quite specific but rather slow and has relatively low sensitivity, unless the system allows time for signal accumulation. Spectrophotometry in the UV and visible range often has good sensitivity and speed, but the specificity may be poor because absorbance bands are broad and intermediates may have chromophoric properties similar to those of the reactant and/or product. Vibrational Spectrophotometry can be better if the IR bands are sharp, as in the case of metal carbonyls, but the solvent must be chosen to provide an appropriate spectral window.
Conference papers on the topic "Absorbance interference study"
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Mahmoud, Mohamed, Ahmed Alsalman, and Hassan Almalki. "Novel Sample Pretreatment to Determine Iron Counts in Sour Glycol Streams by Spectrophotometer." In International Petroleum Technology Conference. IPTC, 2021. http://dx.doi.org/10.2523/iptc-21372-ms.
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Abstract Determination of Iron Content in Triethylene glycol (TEG) samples is a very important indicator in measuring the system corrosion rate in oil and gas facilities. This study employed the application of an alternative/easy and reliable test method, which involved the use of a spectrophotometer for quantification of Iron concentration in tri ethylene glycol samples, that are used in sour gas dehydration units, rather than the sophisticated technique of Inductively Coupled Plasma Optical Emission Spectroscopy, ICP-OES. The main challenge was how to eliminate/minimize the significant interference from the carryover condensate hydrocarbons, BTEX, H2S and amine additives, which cause either precipitation with spectrophotometer reagents or turbid samples. The sample pretreatment process included: 1 - Sample digestion with dilution to eliminate the dissolved acid gases and the dissolved BTEX from the sample in acidic medium; 2 - pH adjustment from 9 – 10.5 to eliminate the amine additives interference with spectrophotometer reagents and 3 – Application of standard addition technique with certified reference material for iron with dilution, to reach the spectrophotometer detection limit and give intense color with more UV absorbance. The method was validated against ICP-OES and the results variance were within 10% acceptance criteria.