Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/6876
Title: An optical fibre reflectance sensor for p-aminophenol determination based on tetrahydroxycalix[4]arene as sensing reagent
Authors: Filik, H.
Aksu, D.
Apak, R.
Şener, İzzet
Kiliç, E.
Keywords: Optical fibre
p-Aminophenol
Reflectance sensor
Tetrahydroxycalix[4]arene
Body fluids
Chemical oxygen demand
Effluents
Fibers
Nitrogen compounds
Optical fibers
Optical materials
Phenols
Reflection
Semiconductor switches
Statistics
Wastewater
Wastewater treatment
Acetylsalicylic acids
Amberlite xad
Amino-phenols
Analyte
Before and after
Common ions
Complex samples
Concentration levels
Concentration ranges
Life-times
Limit of detections
Linear calibration curves
Optic sensors
Optical sensing
Optical-
Oxidation products
Pharmaceutical wastewaters
Reflectance measurements
Reflectance spectrometries
Relative standard deviations
Response times
Sensor responses
Standard deviations
Sensors
Abstract: A fibre-optic sensor for p-aminophenol (PAP) based on the use of 25,26,27,28-tetrahydroxycalix[4]arene (CAL4) immobilised onto Amberlite XAD-16 and reflectance spectrometry has been developed. The sensor is based on the reaction of PAP with CAL4 in presence of an oxidant to produce an indophenol dye. The reflectance measurements were carried out at a wavelength of 620 nm since it yielded the largest divergence different in reflectance spectra before and after reaction with the analyte. A highly linear calibration curve (r2 = 0.992) was observed in the PAP concentration range of 0.5-35 ppm (linear within 0.5-5.5 ppm) with a calculated limit of detection (LOD), defined as the lowest concentration level of analyte that the proposed method can detect to be statistically different from an analytical blank (i.e., yielding an analytical response greater than three times the standard deviation of a blank), of 0.109 ppm. The sensor response from different probes (n = 5) gave an RSD of 1.8% at 10.9 ppm PAP concentration. The response time of the optical one-shot sensor was 5 min for a stirred solution. The intra- and inter-assay variability (as relative standard deviation: RSD) was approximately 2 and 4%, respectively. The lifetime of the blank sensor (CAL4 adsorbed onto XAD-16) was at the order of weeks-months when protected from light, while of the analyte sensor (XAD-16 + CAL4, to which the oxidation product of PAP is coupled) was at the order of days when protected from air and light. Using the optical sensing probe, PAP in urine, pharmaceutical and pharmaceutical wastewater was determined. Although aminophenols showed serious interference, the method was not affected from common ions and from various important drug active constituents present in urine and pharmaceutical effluents such as acetaminophen, acetylsalicylic acid, sorbitol, and caffeine. The proposed technique was tested by replicate analysis of several complex samples with spiked PAP, with recoveries ranging between 97 and 102%. © 2008 Elsevier B.V. All rights reserved.
URI: https://hdl.handle.net/11499/6876
https://doi.org/10.1016/j.snb.2008.11.011
ISSN: 0925-4005
Appears in Collections:Fen-Edebiyat Fakültesi Koleksiyonu
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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