Solid-phase spectrophotometric and visual test-methods of fluoride and oxalate determination are proposed. The methods are based on the competitive reactions of ZrOCl2 with methylthymol blue immobilized on silica gel and fluoride or oxalate in solution. Absorbance of the solid-phase reagent at 590 nm decreases with the growth of fluoride and oxalate contents in solution. The developed methods demonstrate high selectivity. The interference of Bi(III) and SO4(2-), PO4(3-) is eliminated by the addition of 0.01 mol L(-1) solution of ascorbic acid and 0.01 mol L(-1) of BaCl2, respectively. To eliminate the fluoride interference with oxalate determination 1x10(-3) mol L(-1) solution of Ca(NO3)2 at pH 1.5 was added. The anions of the organic acids were destructed prior to F- determination by ultrasonic exposition (44 kHz, intensity of < or = 10 W cm(-2) for 3 min). The proposed methods were applied to the analysis of mineral water, toothpaste and biological fluids.
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http://dx.doi.org/10.1016/j.aca.2007.06.029 | DOI Listing |
Int J Legal Med
December 2024
Division of Forensic Medicine and Toxicology, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Anzio Road, Cape Town, South Africa.
Adverse drug reactions and fatalities can result from therapeutic drug use due to genetic deficiencies in drug-metabolizing enzymes. In cases where ancillary testing may not reveal a clear cause of death, molecular autopsies can be valuable. However, forensic mortuaries do not retain DNA samples in all cases, which hinders subsequent genetic testing if it is later deemed necessary.
View Article and Find Full Text PDFRapid Commun Mass Spectrom
February 2025
Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Canada.
Alkali metals have been used to degrade SF in liquid ammonia. The products include metal fluorides. In this study, we reacted K and Ag with SF in a triple quadrupole mass spectrometer.
View Article and Find Full Text PDFNature
November 2024
Hefei National Research Center for Physical Sciences at the Microscale, Department of Chemistry, University of Science and Technology of China, Hefei, China.
Polyfluoroalkyl and perfluoroalkyl substances (PFASs) are found in many everyday consumer products, often because of their high thermal and chemical stabilities, as well as their hydrophobic and oleophobic properties. However, the inert carbon-fluorine (C-F) bonds that give PFASs their properties also provide resistance to decomposition through defluorination, leading to long-term persistence in the environment, as well as in the human body, raising substantial safety and health concerns. Despite recent advances in non-incineration approaches for the destruction of functionalized PFASs, processes for the recycling of perfluorocarbons (PFCs) as well as polymeric PFASs such as polytetrafluoroethylene (PTFE) are limited to methods that use either elevated temperatures or strong reducing reagents.
View Article and Find Full Text PDFBMC Oral Health
November 2024
Ege University Faculty of Dentistry Department of Prosthodontics, İzmir, Turkey.
Background: The purpose of the study is to evaluate the effect of 7 different desensitizing agents on the shear bond strength (SBS) of zirconia restorations to dentin with a self-adhesive resin cement and determine the failure modes.
Methods: Eighty molars' occlusal surfaces were ground to expose dentin and were randomly divided into 8 groups (n = 10): 1. Gluma (HEMA/Glutaraldehyde) 2.
Nature
November 2024
University of Oxford, Chemistry Research Laboratory, Oxford, UK.
The dangerous chemical hydrogen fluoride sits at the apex of the fluorochemical industry, but the substantial hazards linked to its production under harsh conditions (above 300 degrees Celsius) and transport are typically contracted to specialists. All fluorochemicals for applications, including refrigeration, electric transportation, agrochemicals and pharmaceuticals, are prepared from fluorspar (CaF) through a procedure that generates highly dangerous hydrogen fluoride. Here we report a mild method to obtain fluorochemicals directly from fluorspar, bypassing the necessity to manufacture hydrogen fluoride.
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