The excessive uptake of nitrite is perilous and detrimental for human health that prone to cancer disease. Herein, described the synthesis of SiO/AlO/C material through the sol-gel procedure followed by grafting with 3-n propylpyridinium silsesquioxane chloride organic ligand for enhancing electrochemical activity. H-NMR, C NMR, and Si studies were performed for confirmation of surface functionalization through the grafting technique. The surface morphology was evaluated through SEM and TEM techniques. The material showed an irregular and flakes-like structure that exhibited more compactness and conglomerate structure with no segregation in phase was observed after grafting. The elemental composition was confirmed from EDX analysis. The electrochemical measurements were performed with cyclic voltammetry, electrochemical impedance spectroscopy (EIS), and chronoamperometry. The prepared hybrid inorganic-organic composite Si/C/Al/SiPyCl was applied for the modification of the glassy carbon (GC) electrode and assessed as a sensor for nitrite determination. The sensor showed the low limit of detection (0.01 μM), low limit of quantification (0.08 μM), wide linear response range (0.2-280 μM), and high sensitivity (410 μA·μM). It gave a quick response time of <1 s in the presence of 70 μM nitrite. The fabricated sensor showed high sensitivity, chemical stability, and insignificant interference from co-existing species present in sausage meat and food industry discharges. The repeatability of the sensor was evaluated as 2.5 % R.S.D.; for n = 10 at 50 μM nitrite.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.foodchem.2021.130970 | DOI Listing |
Food Chem
February 2022
Interdisciplinary Research Centre in Biomedical Materials (IRCBM), COMSATS University Islamabad, Lahore Campus, Defence Road, Off Raiwind Road Lahore, 54000, Pakistan. Electronic address:
The excessive uptake of nitrite is perilous and detrimental for human health that prone to cancer disease. Herein, described the synthesis of SiO/AlO/C material through the sol-gel procedure followed by grafting with 3-n propylpyridinium silsesquioxane chloride organic ligand for enhancing electrochemical activity. H-NMR, C NMR, and Si studies were performed for confirmation of surface functionalization through the grafting technique.
View Article and Find Full Text PDFJ Nanosci Nanotechnol
April 2011
Department de Química, Universidade Estadual de Ponta Grossa, 84030-900, Ponta Grossa - PR, Brazil.
Nanostructured films comprising a 3-n-propylpyridinium silsesquioxane polymer (designated as SiPy+Cl-) and copper (II) tetrasulfophthalocyanine (CuTsPc) were produced using the Layer-by-Layer technique (LbL). To our knowledge this is the first report on the use of silsesquioxane derivative polymers as building blocks for nanostructured thin films fabrication. Deposition of the multilayers were monitored by UV-Vis spectroscopy revealing the linear increment in the absorbance of the Q-band from CuTsPc at 617 nm with the number of SiPy+Cl-/CuTsPc or CuTsPc/SiPy+Cl-bilayers.
View Article and Find Full Text PDFJ Colloid Interface Sci
June 2007
Instituto de Quimica, Universidade Estadual de Campinas, C. Postal 6154, 13084-862 Campinas, SP, Brazil.
The quantitative description of cooperativity effects at binding of low-molecular reagents with active reactive centers of hybrid materials requires the elaboration of convenient and reliable meaningful models and calculation procedures. The model of fixed polydentate centers was analyzed as a prospective tool for simulation of adsorption equilibria. The model was shown to be flexible and adaptive.
View Article and Find Full Text PDFJ Colloid Interface Sci
July 2004
Instituto de Química, Unicamp, C.P. 6154, 13084-971 Campinas, Saõ Paulo, Brazil.
Porous Al2O3 presenting a specific surface area of SBET = 105 m2 g(-1) was coated with 3-N-propylpyridinium chloride silsesquioxane polymer. The ion exchange capacity of this polymer grafted onto an Al2O3 surface, resulting in a material designated as AlSiPy(+)Cl-, was 1.09 mmol g(-1).
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!