Search

The interaction of metal oxide nanoparticles with plants has not been extensively studied. An attempt has been made to examine the potential variation in peanut plant leaves due to the application of Fe 2 O 3 nanoparticle by pre-sowing technique and to compare with its bulk counterpart. Fe 2 O 3 nanoparticle was synthesized by chemical route and characterized using X-ray diffraction, atomic force and scanning electron microscopy. The Fe 2 O 3 nanoparticle and its bulk counterpart are applied to the peanut seeds by pre-soaking method at two different concentrations: 500 and 4000 ppm. A total of three replicates were chosen for each morphological and physiological measurement (at an average of three plants per replica). The Fourier transform infrared spectral analysis shows the most prominent peaks at 2923 and 1636 cm −1 , and other peaks vary due to Fe 2 O 3 stress, which was confirmed by the calculated mean ratio of the peak intensities for various frequency regions. All leaf samples show considerable increase in glycoprotein, with 500 ppm bulk and 4000 ppm nano-Fe 2 O 3 samples exhibiting a maximum increase of 73.86% and 71.45%, respectively. The total amide I and II protein content of leaf sample soaked in 500 ppm bulk Fe 2 O 3 suspension decreased to a greater extent compared with other leaf samples. The leaf samples soaked in 500 ppm concentration of both bulk and nano-Fe 2 O 3 suspension exhibited lower lipid content with total band area of 76.97 ± 0.832 and 76.31 ± 0.468, respectively. The cumulative percentage of explained variance in secondary structure of protein of all leaf samples is 83.888% in which factor 1 accounts for 51.870% and factor 2 accounts for 32.018% of the total data variance. The principal component (PC) loadings plot for the spectral range 1600–1700 cm −1 clearly shows that the PC1 factor might establish the maximum variation of the secondary structure of protein in leaf samples. [ABSTRACT FROM AUTHOR]

Multi-component CaF 2 −ZnO–Bi 2 O 3 −P 2 O 5 glasses doped with different concentrations of CoO (ranging from 0 to 1.0 mol %) were crystallized by heat treatment. These samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), EDS and differential thermal analysis (DTA) techniques. The XRD patterns have indicated the presence of various phases viz., Ca 3 (PO 4 ) 2 , Bi 3 PO 7 , CaZn 2 (PO 4 ) 2 , Bi(PO 4 ), Zn 3 (PO 4 ) 2 , ZnCo(P 2 O 7 ), CaCoP 2 O 7 , ZnCo 2 O 4 , CoF 2 , Co 3 O 4 and CoF 3 . Conventional spectroscopic studies such as optical absorption, FTIR and Raman were also carried out on these glass ceramic samples. The analysis of these results has indicated that cobalt ions exist in both Co 2+ and Co 3+ states in the glass ceramic network. These studies have further revealed that the rigidity of the glass ceramic network decreases up to 0.6 mol% of CoO. Beyond this concentration the insulating strength of the prepared samples is found to increase. [ABSTRACT FROM AUTHOR]

Nickel ferrite NiFeO nanoparticles (NPs) were successfully synthesized by using nickel nitrate, ferric nitrate, citric acid, and ethyl cellulose as a surfactant by a simple sol-gel-assisted combustion method (SACM) and microwave-assisted combustion method (MACM). Structural, morphological, optical, and magnetic properties of the obtained powder were characterized by powder X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), photoluminescence (PL) spectroscopy, and vibrating sample magnetometry (VSM). XRD results show that the resultant powder was pure crystalline with cubic structure. The average crystalline size was found to be 18.8 and 10.2 nm synthesized by SACM and MACM, respectively. FT-IR spectra indicate the type of bonds between Ni-O and Fe-O (metal and oxygen). SEM images show that the morphology of the powder consists of well-defined structure. VSM results showed a ferromagnetic behavior of the sample. Antimicrobial activity of NiFeO nanoparticles was performed. Both sample 1 (SACM) and sample 2 (MACM) show good inhibition in the zone 100 μg/ml. While comparing, sample 2 shows high inhibition than sample 1. [ABSTRACT FROM AUTHOR]