Biosynthesis of Iron and Cobalt Nanoparticles Using Garlic (Allium cativum) Extract and their Some Applications

2021 ◽  
Vol 882 ◽  
pp. 165-170
Author(s):  
Wisam J. Aziz ◽  
Marwa Abdul Muhsien Hassan ◽  
Mohammed Jwad Khadam
Keyword(s):  
Pathogenic Bacteria ◽  
Chemical Method ◽  
Cobalt Nanoparticles ◽  
Nano Particles ◽  
Cubic Phase ◽  
Oxidizing Agent ◽  
X Ray Diffraction ◽  
X Ray ◽  
E Coli ◽  
Jcpds Card

It has been employed nano particles using garlic (Allium cativum) extract at conditions (pH=12, concentration = 0.1 M, temperature = 90 °C, time =3 hr. and Oxidizing agent (hydrozoan). X-Ray diffraction of Co NPs using Allium cativum with polycrystalline as compared to specification (JCPDS Card no. 030-0443) and the structure is cubic phase and showed nothing at any article than to extract used as search (chemical) method with the outfit that successful chemical picas distinct and no trace of moisture dust concentrations are enlargement were appropriate for the sample. XRD of Fe NPs using Allium cativum is polycrystalline depend on (JCPDS Card no. 052-0513) with peaks (111, 200, 220) and 2θ(42.7, 49.7, 73.1). FESEM pictures of cobalt and Iron nano particles. The nano particles morphology demonstrates irregular, cubic and hexagonal pattern of different sizes which are agglomerated. Other findings with larger magnifications show that all these pictures have soft surfaces. Co NPs / Fe NPs / c-Si n-type (100) structure has a better performance against Co NPs/Si n-type (100) and Fe NPs /Si n-type (100) structures, such that the output of solar cells efficiencies are 6.31, 7.03 and 7.8 % respectively. Cobalt and iron nanostructures produced naturally used to have anti bacterial behavior against pathogenic bacteria such as B-cereus and E-coli with (37, 39) mm, respectively.

Green Biosynthesis of Iron Oxide Nanoparticles and Testing Their Inhibitory Efficacy Against Some Pathogens

2021 ◽  
Vol 18 (4) ◽  
pp. 119-123
Author(s):  
Doaa Kaduim ◽  
Zaid Mahmoud ◽  
Falah Mousa
Keyword(s):  
Iron Oxide ◽  
Beta Vulgaris ◽  
Inhibition Zone ◽  
Nano Particles ◽  
X Ray Diffraction ◽  
X Ray ◽  
E Coli ◽  
Size Of Particles ◽  
Xrd Patterns ◽  
Antibacterial And Antifungal

The biosynthesis of iron oxide (Fe2O3, also known as haematite) nano particles (NPs) using Hydra helix and Beta vulgaris aqueous extracts were adduced, respectively, where the extracts act as a stabiliser and reductant reagent. The crystal structure and size of particles were investigated using X-ray diffraction (XRD), while the morphology was examined using field emission scanning electron microscopy (FESEM), XRD patterns showed the synthesised nanoparticles with well-crystallised structure from Beta vulgaris extract with size 12 nm, while the results by using Hydra helix showed many peaks back to Goethite phase with 16 nm. The antibacterial and antifungal activity were examined using Staphylococcus (showed inhibition zone diameter 23 mm, 16 mm using Hydra helix and Beta vulgaris, respectively), E. coli (showed no inhibition) and Candida fungi (showed inhibition zone 16 mm, 11 mm using Hydra helix and Beta vulgaris, respectively).

One-Step Synthesis of BaCO3 Nano-Particles via Mechano-Chemical Method

2012 ◽  
Vol 622-623 ◽  
pp. 985-989
Author(s):  
H. Akbari Moayyer ◽  
A. Ataie ◽  
Amin Nozari ◽  
Saeed Jafari
Keyword(s):  
Chemical Method ◽  
Milling Time ◽  
Barium Carbonate ◽  
Phase Evolution ◽  
Nano Particles ◽  
X Ray Diffraction ◽  
Chemical Route ◽  
X Ray ◽  
One Step ◽  
Scanning Electron

Barium carbonate (BaCO3) nano-particles were synthesized from the mixture of Ba(OH)2.8H2O and Na2CO3 by mechano-chemical route without any subsequent heat treatment of the as-milled powders. Effects of milling time and addition of process control agents (PCA) on the phase composition and morphology of products have been investigated. The samples were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). XRD results show that BaCO3 nano-particles were synthesized only after 10 minutes of mechanical milling and phase evolution was not taken place by further milling. SEM results indicated that pencil-like and globular-like were two major morphologies of the particles. Addition of stearic acid as a PCA resulted in homogenized globular-like nano-particles with a mean particle size of 54 nm.

Ribosome Structural Organization

1974 ◽  
Vol 32 ◽  
pp. 332-333
Author(s):  
James A. Lake
Keyword(s):  
Ribosomal Proteins ◽  
Structural Organization ◽  
Three Dimensional ◽  
Small Subunit ◽  
Structural Studies ◽  
X Ray Diffraction ◽  
Specific Antibodies ◽  
X Ray ◽  
E Coli ◽  
Complete Sequences

The understanding of ribosome structure has advanced considerably in the last several years. Biochemists have characterized the constituent proteins and rRNA's of ribosomes. Complete sequences have been determined for some ribosomal proteins and specific antibodies have been prepared against all E. coli small subunit proteins. In addition, a number of naturally occuring systems of three dimensional ribosome crystals which are suitable for structural studies have been observed in eukaryotes. Although the crystals are, in general, too small for X-ray diffraction, their size is ideal for electron microscopy.

RNA polymerase: Preparation and structural analysis of helical polymers

1984 ◽  
Vol 42 ◽  
pp. 152-153
Author(s):  
E. Loren Buhle ◽  
Pamela Rew ◽  
Ueli Aebi
Keyword(s):  
Structural Analysis ◽  
Rna Polymerase ◽  
Molecular Level ◽  
X Ray Diffraction ◽  
Helical Polymers ◽  
X Ray ◽  
E Coli ◽  
The Past ◽  
Ordered Arrays ◽  
Low Ionic Strength

While DNA-dependent RNA polymerase represents one of the key enzymes involved in transcription and ultimately in gene expression in procaryotic and eucaryotic cells, little progress has been made towards elucidation of its 3-D structure at the molecular level over the past few years. This is mainly because to date no 3-D crystals suitable for X-ray diffraction analysis have been obtained with this rather large (MW ~500 kd) multi-subunit (α2ββ'ζ). As an alternative, we have been trying to form ordered arrays of RNA polymerase from E. coli suitable for structural analysis in the electron microscope combined with image processing. Here we report about helical polymers induced from holoenzyme (α2ββ'ζ) at low ionic strength with 5-7 mM MnCl2 (see Fig. 1a). The presence of the ζ-subunit (MW 86 kd) is required to form these polymers, since the core enzyme (α2ββ') does fail to assemble into such structures under these conditions.

A New Polyethylene Corrosion Protecting Coating with Ion Selectivity

2011 ◽  
Vol 314-316 ◽  
pp. 273-278
Author(s):  
Yu Hua Dong ◽  
Ke Ren ◽  
Qiong Zhou
Keyword(s):  
Ion Selectivity ◽  
Nano Particles ◽  
Ammonium Bromide ◽  
Linear Low Density Polyethylene ◽  
X Ray Diffraction ◽  
Sulfosalicylic Acid ◽  
X Ray ◽  
Chemically Modified ◽  
Before And After ◽  
Industrial Standards

Linear low density polyethylene (LLDPE) was chemically modified with grafting maleic anhydride (MAH) monomer on its backbone by melting blending. Nano-particles SiO2 was modified by cationic surfactant hexadecyl trimethyl ammonium bromide (CTAB) and anionic surfactant sulfosalicylic acid (SSA) and added to PE coating respectively. Measurement of membrane potential showed that the coating containing modified SiO2 nano-particles had characteristic of ion selectivity. The properties of the different coatings were investigated according to relative industrial standards. Experimental results indicated that PE coating with ion selectivity had better performances, such as adhesion strength, cathodic disbonding and anti-corrosion, than those of coating without ion selectivity. Crystal structure of the coatings before and after alkali corrosion was characterized by Fourier transform infrared spectra (FTIR) and X-ray diffraction (XRD). Structure of the coating without ion selectivity was damaged by NaOH alkali solution, causing mechanical properties being decreased. And the structure of the ion selective coatings was not affected.

scholarly journals Transport and Dielectric Properties of Mechanosynthesized La2/3Cu3Ti4O12 Ceramics

Crystals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 313
Author(s):  
Mohamad M. Ahmad ◽  
Hicham Mahfoz Kotb ◽  
Celin Joseph ◽  
Shalendra Kumar ◽  
Adil Alshoaibi
Keyword(s):  
Dielectric Constant ◽  
Sintering Temperature ◽  
Cubic Phase ◽  
X Ray Diffraction ◽  
Boundary Conductivity ◽  
X Ray ◽  
Giant Dielectric ◽  
Mechanochemical Milling ◽  
Giant Dielectric Constant ◽  
Lower Temperature

La2/3Cu3Ti4O12 (LCTO) powder has been synthesized by the mechanochemical milling technique. The pelletized powder was conventionally sintered for 10 h at a temperature range of 975–1025 °C, which is a lower temperature process compared to the standard solid-state reaction. X-ray diffraction analysis revealed a cubic phase for the current LCTO ceramics. The grain size of the sintered ceramics was found to increase from 1.5 ± 0.5 to 2.3 ± 0.5 μm with an increase in sintering temperature from 975 to 1025 °C. The impedance results show that the grain conductivity is more than three orders of magnitude larger than the grain boundary conductivity for LCTO ceramics. All the samples showed a giant dielectric constant (1.7 × 103–3.4 × 103) and dielectric loss (0.09–0.17) at 300 K and 10 kHz. The giant dielectric constant of the current samples was attributed to the effect of internal barrier layer capacitances due to their electrically inhomogeneous structure.

Energy Band Gap Studies of CdS Nanomaterials

2008 ◽  
Vol 3 ◽  
pp. 97-102 ◽  
Author(s):  
Dinu Patidar ◽  
K.S. Rathore ◽  
N.S. Saxena ◽  
Kananbala Sharma ◽  
T.P. Sharma
Keyword(s):  
Optical Absorption ◽  
Band Gap ◽  
Energy Band ◽  
Chemical Method ◽  
Optical Absorption Spectroscopy ◽  
Cds Nanoparticles ◽  
X Ray Diffraction ◽  
Energy Band Gap ◽  
X Ray ◽  
Simple Chemical

The CdS nanoparticles of different sizes are synthesized by a simple chemical method. Here, CdS nanoparticles are grown through the reaction of solution of different concentration of CdCl2 with H2S. X-ray diffraction pattern confirms nano nature of CdS and has been used to determine the size of particle. Optical absorption spectroscopy is used to measure the energy band gap of these nanomaterials by using Tauc relation. Energy band gap ranging between 3.12 eV to 2.47 eV have been obtained for the samples containing the nanoparticles in the range of 2.3 to 6.0 nm size. A correlation between the band gap and size of the nanoparticles is also established.

Stacking Faults in a High Nitrogen Face-Centered-Cubic Phase Formed on Nitrogen-Modified Austenitic Stainless Steel

2008 ◽  
Vol 373-374 ◽  
pp. 318-321
Author(s):  
J. Liang ◽  
M.K. Lei
Keyword(s):  
Stainless Steel ◽  
Plasma Source ◽  
Peak Shift ◽  
Cubic Phase ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
High Nitrogen ◽  
X Ray ◽  
Peak Asymmetry ◽  
Face Centered

Effects of stacking faults in a high nitrogen face-centered-cubic phase (γΝ) formed on plasma source ion nitrided 1Cr18Ni9Ti (18-8 type) austenitic stainless steel on peak shift and peak asymmetry of x-ray diffraction were investigated based on Warren’s theory and Wagner’s method, respectively. The peak shift from peak position of the γΝ phase is ascribed to the deformation faults density α, while the peak asymmetry of the γΝ phase is characterized by deviation of the center of gravity of a peak from the peak maximum (Δ C.G.) due to the twin faults density β. The calculated peak positions of x-ray diffraction patterns are consistent with that measured for plasma source ion nitrided 1Cr18Ni9Ti stainless steel.

scholarly journals Characterization of ferrite nanoparticles for preparation of biocomposites

2017 ◽  
Vol 8 ◽  
pp. 1257-1265 ◽  
Author(s):  
Urszula Klekotka ◽  
Magdalena Rogowska ◽  
Dariusz Satuła ◽  
Beata Kalska-Szostko
Keyword(s):  
Chemical Method ◽  
Ferrite Nanoparticles ◽  
Chemical Activity ◽  
Nominal Composition ◽  
X Ray Diffraction ◽  
Wet Chemical Method ◽  
X Ray ◽  
Transmission Electron ◽  
Wet Chemical

Ferrite nanoparticles with nominal composition Me0.5Fe2.5O4 (Me = Co, Fe, Ni or Mn) have been successfully prepared by the wet chemical method. The obtained particles have a mean diameter of 11–16 ± 2 nm and were modified to improve their magnetic properties and chemical activity. The surface of the pristine nanoparticles was functionalized afterwards with –COOH and –NH2 groups to obtain a bioactive layer. To achieve our goal, two different modification approaches were realized. In the first one, glutaraldehyde was attached to the nanoparticles as a linker. In the second one, direct bonding of such nanoparticles with a bioparticle was studied. In subsequent steps, the nanoparticles were immobilized with enzymes such as albumin, glucose oxidase, lipase and trypsin as a test bioparticles. The characterization of the nanoparticles was acheived by transmission electron microscopy, X-ray diffraction, energy dispersive X-ray and Mössbauer spectroscopy. The effect of the obtained biocomposites was monitored by Fourier transform infrared spectroscopy. The obtained results show that in some cases the use of glutaraldehyde was crucial (albumin).

A Study on the Growth of Cubic GaN Films Using an AlGaAs Buffer Layer Grown on GaAs (100) by Plasma-Assisted Molecular Beam Epitaxy

2000 ◽  
Vol 639 ◽  
Author(s):  
Ryuhei Kimura ◽  
Kiyoshi Takahashi ◽  
H. T. Grahn
Keyword(s):  
Molecular Beam Epitaxy ◽  
Buffer Layer ◽  
Molecular Beam ◽  
High Energy ◽  
Rf Plasma ◽  
Cubic Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Cubic Gan

ABSTRACTAn investigation of the growth mechanism for RF-plasma assisted molecular beam epitaxy of cubic GaN films using a nitrided AlGaAs buffer layer was carried out by in-situ reflection high energy electron diffraction (RHEED) and high resolution X-ray diffraction (HRXRD). It was found that hexagonal GaN nuclei grow on (1, 1, 1) facets during nitridation of the AlGaAs buffer layer, but a highly pure, cubic-phase GaN epilayer was grown on the nitrided AlGaAs buffer layer.

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