Green synthesis of Mangifera indica silver nanoparticles and its analysis using Fourier transform infrared and scanning electron microscopy

2017 ◽  
pp. 1 ◽  
Author(s):  
Bharathi V ◽  
Jannathul Firdous ◽  
Noorzaid Muhamad ◽  
Resni Mona
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Silver Nanoparticles ◽  
Fourier Transform ◽  
Green Synthesis ◽  
Mangifera Indica ◽  
Fourier Transform Infrared ◽  
Its Analysis ◽  
Scanning Electron

PENINGKATAN LAJU DISOLUSI ACYCLOVIR DENGAN METODE SISTEM DISPERSI PADAT MENGGUNAKAN POLOXAMER 188

2016 ◽  
Vol 5 (1) ◽  
pp. 6
Author(s):  
Budi Setiawan ◽  
Erizal Zaini ◽  
Salman Umar
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Differential Thermal Analysis ◽  
Fourier Transform Infrared ◽  
X Ray Diffraction ◽  
Poloxamer 188 ◽  
X Ray ◽  
Scanning Electron

Sebuah penelitian tentang sistem dispersi padat dari asiklovir dengan poloxamer 188 telah dilakukan formulasi dengan pencampuran secara fisika dengan rasio 1 : 1, 1 : 3, 1 : 5 dan dispersi padat 1 : 1, 1 : 3, 1 : 5 dan penggilingan 1:1 sebagai pembanding. Dispersi padat dibuat menggunakan metode pencairan (fusi), yang digabung dengan poloxamer 188 pada hotplate kemudian asiklovir dimasukkan ke dalam hasil poloxamer 188 lalu di kocok hingga membentuk masa homogen. Semua formula yang terbentuk termasuk asiklovir poloxamer 188 murni dianalisis karakterisasinya dengan Differential Thermal Analysis (DTA), X-ray Diffraction, Scanning Electron Microscopy (SEM), dan Fourier Transform Infrared (FTIR), kemudian pengambilan dilakukan  (penentuan kadar) mengunakan spektrofotometer UV pada panjang gelombang 257,08 nm dan uji laju disolusi dengan aquadest bebas CO2 menggunakan metode dayung. Hasil pengambilan  (penentuan kadar) menunjukkan bahwa semua formula memenuhi persyaratan farmakope Amerika edisi 30 dan farmakope Indonesia edisi 4 yaitu 95-110%. Sedangkan hasil uji laju disolusi untuk campuran fisik 1: 1, dan dispersi padat 1: 1, dan penggilingan 1: 1 menunjukkan peningkatan yang nyata dibandingkan asiklovir murni. Hal ini juga dapat dilihat dari hasil perhitungan statistik  menggunakan analisis varian satu arah  SPSS 17.

Effect of Dibenzyl Disulfide Corrosion on Accelerated Thermal Aging Crosslinked Polyethylene Cable Materials with Copper Core and Insulation Layer

2020 ◽  
Vol 15 (11) ◽  
pp. 1406-1411
Author(s):  
Yi-Fan Cheng ◽  
Ling-Na Xu ◽  
Tian-En Chen ◽  
Guo-Zhen Jiang ◽  
Jia-Bin Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Thermal Aging ◽  
Fourier Transform Infrared ◽  
Element Distribution ◽  
Insulation Layer ◽  
Xlpe Cable ◽  
Scanning Electron ◽  
Accelerated Thermal Aging

Crosslinked polyethylene (XLPE) cable has been widely used and studied with its specific failure mechanism. Among them, although thermal aging of XLPE insulation materials has been widely studied, the effect of accelerated thermal aging on the sulfur corrosion of XLPE cable has not been studied much. For further understand the mechanism of sulfur corrosion, the accelerated thermal aging method was taken with 200 mg/kg DBDS based on the distinguish of temperature. The macro and micro analysis contrast test before and after corrosion were also taken to investigate the morphology difference, the element distribution, the influence of thermal aging and DBDS addition the corrosion of copper core, and the assessment of insulation layer was also carried out by Fourier transform infrared spectra and spectroscopy, scanning electron microscopy to distinguish the microstructure and composition. Under the accelerated thermal aging experiment with DBDS, both copper core and insulation layer of sample No. 1 exhibit the most serious corrosion and aging condition. On the surface of the copper core, the DBDS-Cu complexes decompose to produce Cu2S and the temperature has a direct effect on this reaction. The insulation layer of sample No. 1 showed the most severe aging situation, with characteristic peaks of carbonyl appearing at 1720 cm-1 in the Fourier transform infrared tests and more defects, holes and cracks found in spectroscopy, scanning electron microscopy images.

scholarly journals Kesetimbangan Adsorpsi Zat Warna Methyl Violet Oleh Karbon Aktif Berbasis Limbah Daun Nanas (Ananas comosus L)

METANA ◽  
2018 ◽  
Vol 14 (2) ◽  
pp. 31
Author(s):  
Lanjar Lanjar ◽  
Fatma Indah Riayanti ◽  
Widi Astuti
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Surface Area ◽  
Methyl Violet ◽  
Fourier Transform Infrared ◽  
Ananas Comosus ◽  
Ftir Spectrometer ◽  
Model Isotherm ◽  
Scanning Electron

Industri tekstil semakin berkembang seiring dengan pertumbuhan penduduk di Indonesia. Selain memberikan manfaat, industri tekstil  memberikan dampak negatif bagi lingkungan akibat penggunaan zat warna sintetis, salah satunya yaitu methyl violet. Apabila limbah tersebut dibuang ke perairan akan menyebabkan rusaknya ekologi lingkungan dan ancaman bagi kesehatan manusia, karena sebagian besar zat warna bersifat sukar terurai (non-bidegradable) dan karsinogenik (Brono, 2010). Salah satu metode yang terbukti efektif untuk menghilangkan zat warna adalah adsorpsi menggunakan karbon aktif. Pada penelitian ini karbon aktif dibuat dari limbah daun nanas dengan aktivator ZnCl2 dan pemanasan gelombang mikro. Selanjutnya, karbon aktif tersebut dikarakteriasi morfologi permukaan menggunakan Scanning Electron Microscopy (SEM), luas permukaan menggunakan Surface Area Analyzer, dan analisis gugus fungsi menggunakan Fourier Transform Infrared (FTIR) spectrometer, dan digunakan untuk menjerap methyl violet di larutan. Hasil penelitian menunjukkan bahwa karbon aktif dari limbah daun nanas yang teraktivasi ZnCl2 menghasilkan pori yang lebih besar dibandingkan dengan karbon tanpa aktivasi serta memiliki gugus fungsi yang dapat menjerap methyl violet. Kondisi optimum untuk adsorpsi adalah pH 5, waktu kontak 90 menit, dan konsentrasi awal 500 mg/L. Model kesetimbangan yang sesuai yaitu menggunakan model isotherm freundlich.

scholarly journals Influence of Hydroxyapatite Nanospheres in Dentin Adhesive on the Dentin Bond Integrity and Degree of Conversion: A Scanning Electron Microscopy (SEM), Raman, Fourier Transform-Infrared (FTIR), and Microtensile Study

Polymers ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 2948
Author(s):  
Rana S Al-Hamdan ◽  
Basil Almutairi ◽  
Hiba F Kattan ◽  
Noura A. Alsuwailem ◽  
Imran Farooq ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Fourier Transform Infrared ◽  
Study Groups ◽  
Degree Of Conversion ◽  
Hybrid Layer ◽  
X Ray ◽  
And Control ◽  
Scanning Electron

An experimental adhesive incorporated with different nano-hydroxyapatite (n-HA) particle concentrations was synthesized and analyzed for dentin interaction, micro-tensile bond strength (μTBS), and degree of conversion (DC). n-HA powder (5 wt % and 10 wt %) were added in adhesive to yield three groups; gp-1: control experimental adhesive (CEA, 0 wt % HA), gp-2: 5 wt % n-HA (HAA-5%), and gp-3: 10 wt % n-HA (HAA-10%). The morphology of n-HA spheres was evaluated using Scanning Electron Microscopy (SEM). Their interaction in the adhesives was identified with SEM, Energy-Dispersive X-ray (EDX), and Micro-Raman spectroscopy. Teeth were sectioned, divided in study groups, and assessed for μTBS and failure mode. Employing Fourier Transform-Infrared (FTIR) spectroscopy, the DC of the adhesives was assessed. EDX mapping revealed the occurrence of oxygen, calcium, and phosphorus in the HAA-5% and HAA-10% groups. HAA-5% had the greatest μTBS values followed by HAA-10%. The presence of apatite was shown by FTIR spectra and Micro-Raman demonstrated phosphate and carbonate groups for n-HA spheres. The highest DC was observed for the CEA group followed by HAA-5%. n-HA spheres exhibited dentin interaction and formed a hybrid layer with resin tags. HAA-5% demonstrated superior μTBS compared with HAA-10% and control adhesive. The DC for HAA-5% was comparable to control adhesive.

Biocidal activity of curcumin and cationic polymer possessing composites

2020 ◽  
Vol 35 (4-5) ◽  
pp. 389-398
Author(s):  
Tarık Eren ◽  
Gülay Baysal ◽  
Faik Doğan
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Curcuma Longa ◽  
Antibacterial Properties ◽  
Fourier Transform Infrared ◽  
Diffusion Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

There is a growing interest in new type of biocidal compounds with antibacterial properties against bacteria. In this study, new antibacterial synthetic materials bearing curcumin and cationic polymers were synthesized. In the synthesis stage, the methacrylate functional cationic monomer was synthesized via the Michael addition route by using 3-acryloxy-2-hydroxypropyl methacrylate and 3-amino pyridine to obtain Monomer 1. Monomer 1 was further quaternized with hexyl bromide to obtain a cationic methacrylate functional monomer. Free-radical polymerization of Monomer 1 and methyl acrylate was conducted in the presence of azobisisobutyronitrile under dimethylformamide solvent. The composite formulation was conducted by using turmeric extract Curcuma longa (curcumin), hydroxyapatite, montmorillonite, and silver nitrate. The materials were analyzed by using the methods of X-ray diffraction, nuclear magnetic resonance, Fourier transform infrared spectroscopy, and scanning electron microscopy. The biocidal activities against the bacteria Escherichia coli, Listeria monocytogenes, Salmonella, and Staphylococcus aureus were analyzed using agar well diffusion method. From the Fourier transform infrared, X-ray diffraction, and scanning electron microscopy analysis results of the synthesized nanocomposites, it is seen that they form strong connections with the components added to the composites and form an exfoliated structure. According to the antibacterial analysis results, the nanocomposites obtained have showed a strong antibacterial resistance against E.coli, L.monocytogenes, Salmonella, and S. aureus bacteria, and the high inhibition zone areas were obtained.

Ethylenediamine Processed Cu2SnS3 Nano Particles via Mild Solution Route

2016 ◽  
Vol 19 (1) ◽  
pp. 001-005 ◽  
Author(s):  
Paul Nesamony Prathiba Jeya Helan ◽  
Kannusamy Mohanraj ◽  
Sethuramachandran Thanikaikarasan ◽  
Thaiyan Mahalingam ◽  
Ganesan Sivakumar ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Fourier Transform Infrared ◽  
Nano Particles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Electron Microscopy Analysis ◽  
Microscopy Techniques ◽  
Scanning Electron

Copper tin sulphide nanoparticles have been prepared by solution growth technique at various ethylenediamine concentrations. Prepared samples have been characterized using x-ray diffraction, fourier transform infrared, Raman and scanning electron microscopy techniques. x-ray diffraction results revealed that the prepared samples are nanocrystalline in nature with tetragonal structure. Fourier transform infrared spectroscopy analysis results showed the presence of Cu-O, Sn-O and Sn-S vibrations in the wavenumber range between 450 and 620 cm-1. Vibrational symmetry of prepared samples have been analyzed using Raman spectroscopy. Scanning electron microscopy analysis indicated the formation of flower like nanocrystals for samples prepared at various Ethylenediamine concentrations.

Regeneration of the Brewing Spent Diatomite

2014 ◽  
Vol 998-999 ◽  
pp. 1425-1428 ◽  
Author(s):  
Wen Ya Mei ◽  
Teng Hong Hui
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Surface Area ◽  
Fourier Transform Infrared ◽  
X Ray Diffraction ◽  
X Ray ◽  
Remarkable Increase ◽  
Efficient Adsorbent ◽  
Scanning Electron

Brewing spent diatomite (BSDT), a beer industrial by-product, was regenerated with calcination. The characteristics of regenerated BSDT were detected by X-ray diffraction, X-ray fluorescence, Fourier-transform infrared, and scanning electron microscopy. The results showed that the mineralization of the surface adsorbate and the remarkable increase in the Si-OH decreased the pHpzc value from 7.6 to 5.2 and increased the surface area from 36 m2/g to 52 m2/g after calcination at 800 °C. The results show that the regenerated BSTD could be employed as an efficient adsorbent for the recycling of BSDT.

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