S
S.K. Mehta
Researcher at Panjab University, Chandigarh
Publications - 146
Citations - 2711
S.K. Mehta is an academic researcher from Panjab University, Chandigarh. The author has contributed to research in topics: Nanoparticle & Molar volume. The author has an hindex of 26, co-authored 144 publications receiving 2187 citations.
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Tungsten oxide (WO3) nanoparticles as scaffold for the fabrication of hydrazine chemical sensor
TL;DR: In this paper, the fabrication and characterization of hydrazine amperometric sensor based on tungsten oxide (WO3) nanoparticles was reported, which exhibited a good sensitivity of 0.18,471μA/μM/cm2 and detection limit of 144.73μM.
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Photocatalytic degradation of the antibiotic levofloxacin using highly crystalline TiO2 nanoparticles
TL;DR: In this paper, the photocatalytic degradation of levofloxacin (LEVO), a widely used antibiotic drug, using highly crystalline TiO2 nanoparticles was reported.
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Synthesis of CeO2–ZnO nanoellipsoids as potential scaffold for the efficient detection of 4-nitrophenol
Kulvinder Singh,Ahmed Ibrahim,Ahmad Umar,Arun Kumar,Ganga Ram Chaudhary,Sukhjinder Singh,S.K. Mehta +6 more
TL;DR: In this paper, a well-crystalline CeO 2 -ZnO composite nanoellipsoids (NEs) were synthesized by facile hydrothermal process at low-temperature and characterized in detail in terms of their morphological, structural, optical and compositional properties.
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Fabrication of novel carbon quantum dots modified bismuth oxide (α-Bi2O3/C-dots): Material properties and catalytic applications
TL;DR: The synthesized photocatalyst showed superior visible-light driven photocatalytic activity for the degradation of indigo carmine dye and exhibited 79% degradation of antibiotic drug levofloxacin within 120 min, under optimized conditions of pH, catalyst dose and initial dye concentration.
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Formulation of Tyloxapol niosomes for encapsulation, stabilization and dissolution of anti-tubercular drugs
S.K. Mehta,Neha Jindal +1 more
TL;DR: In vitro dissolution studies at physiological conditions have been undertaken to compare the release behavior of drugs from the prepared niosomes and comparison of regression coefficients of different kinetic models reveal that INH release follows Fickian diffusion mechanism whereas RIF and PZA, a non-Fickian release mechanism.