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Journal ArticleDOI

Potassium Iodide as a Chemical Actinometer for 254 nm Radiation: Use of Iodate as an Electron Scavenger

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TLDR
In this paper, a solution of 0.6 M iodide and 0.1 M iodate in 0.01 M borate buffer (pH 9.25) was used as a chemical actinometer to measure the incident fluence from a low-pressure mercury lamp that puts out more than 85% of its energy at 254 nm.
Abstract
— A solution of 0.6 M iodide and 0.1 M iodate in 0.01 M borate buffer (pH 9.25) can be used as a chemical actinometer to measure the incident fluence from a low-pressure mercury lamp that puts out more than 85% of its energy at 254 nm. The actinometric solution is optically opaque to light below 290 nm and is optically transparent to wavelengths greater than 330 nm. Hence, the solution absorbs all of the germicidal wavelengths but little if any of the ambient light normally present in the laboratory. Iodate acts as an electron scavenger and prevents the back reaction of the free electron with the iodine atom following UV excitation of KI. Irradiation results in the linear formation of triiodide, which is quantitated by measuring its absorbance at 352 nm. The quantum yield for this system is approximately 0.75 0.03 at 20.7AoC or approximately three times greater than that obtained previously using nitrous oxide as an electron scavenger. A model is proposed to account for this difference. A precise expression to account for the concentration and temperature dependence of the quantum yield is given by pH = 0.75(1 + 0.23[C - 0.577])(1 + 0.02[T - 20.7]) where C is the concentration of iodide and T is the temperature. The concentration of iodide can be obtained from the absorbance at 300 nm prior to irradiation using 1.061 MJ cm−1 as the molar extinction coefficient. This actinometric system meets the quality criteria established by the International Union of Pure and Applied Chemistry with the caveat that it is designed to measure only germicidal radiation (i.e. wavelengths less than 290 nm).

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Citations
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Standardization of Methods for Fluence (UV Dose) Determination in Bench-Scale UV Experiments

TL;DR: In this article, a detailed protocol for the determination of the fluence (UV dose) in a bench scale UV apparatus containing UV lamps emitting either monochromatic or broadband UV light was developed.
Journal ArticleDOI

DNA-modified nanocrystalline diamond thin-films as stable, biologically active substrates.

TL;DR: It is shown that nanocrystalline diamond thin-films covalently modified with DNA oligonucleotides provide an extremely stable, highly selective platform in subsequent surface hybridization processes, suggesting that diamond thin -films may be a nearly ideal substrate for integration of microelectronics with biological modification and sensing.
Journal ArticleDOI

Kinetic Study of Hydroxyl and Sulfate Radical-Mediated Oxidation of Pharmaceuticals in Wastewater Effluents

TL;DR: In this study, kinetic models were built to predict the degradation of PPCPs in both HO•- and SO4•--mediated oxidation, indicating the dominant role of HO• in the removal of P PCPs.
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Oxidative degradation of atrazine in aqueous solution by UV/H2O2/Fe2+, UV/S2O82-/Fe2+ and UV/HSO5-/Fe2+ processes: A comparative study

TL;DR: In this paper, the degradation of atrazine, a widely used endocrine disrupting, carcinogenic and persistent herbicide, was investigated by photo-Fenton-like advanced oxidation technologies.
Journal ArticleDOI

Quantum Yield of the Iodide–Iodate Chemical Actinometer: Dependence on Wavelength and Concentration¶

TL;DR: The results showed a 20% reduction in QY between 240 and 280 nm as compared with radiometry, which suggests that the QY of the ferrioxalate actinometer in this region of the spectrum needs reexamination.
References
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Journal ArticleDOI

A compilation of specific bimolecular rate constants for the reactions of hydrated electrons, hydrogen atoms and hydroxyl radicals with inorganic and organic compounds in aqueous solution

TL;DR: In this paper, a compilation of the available kinetic data on the reactivities of the primary species of radiolysis in aqueous solution is presented, covering hydrated electrons, hydrogen atoms and hydroxyl radicals.
Journal ArticleDOI

A New Sensitive Chemical Actinometer. I. Some Trials with Potassium Ferrioxalate

TL;DR: A chemical actinometer has been devised whose high sensitivity and precision depends upon the spectrophotometric determination of the photolysis products of potassium ferrioxalate with 1:10 phenanthroline as discussed by the authors.
Journal ArticleDOI

Spectrophotometric determination of hydrogen peroxide and organic hydropheroxides at low concentrations in aqueous solution

TL;DR: In this paper, five procedures are presented for the determination of hydrogen peroxide and organic hydroperoxides (including organic peroxyacids) at concentrations of 1-10 μM in aqueous soltion.
Journal ArticleDOI

Rate constant for scavenging eaq- in nitrous oxide-saturated solutions

TL;DR: In this article, the rate constant for reaction of hydrated electrons with N/sub 2/O in aqueous solutions has been determined to be (9.1 +- 0.2) x 10/sup 9/ M/sup -1/ s/sup −1/s/sup 1/1/
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