Analysis of Urinary Stones Collected from Some Patients with X-Ray Diffraction, Fourier Transform Infrared Spectroscopy, and Scanning Electron Microscopy

2019 ◽  
Vol 85 (6) ◽  
pp. 1050-1057
Author(s):  
M. Serkan Yalçın ◽  
Mesut Tek
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Fourier Transform Infrared Spectroscopy ◽  
Fourier Transform Infrared ◽  
Urinary Stones ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

scholarly journals The Characteristics of Padamarang Magnesite under Calcination and Hydrothermal Treatment

2019 ◽  
Vol 29 (2) ◽  
Author(s):  
Mutia Dewi Yuniati ◽  
Feronika Cinthya Mawarni Putri Wawuru ◽  
Anggoro Tri Mursito ◽  
Iwan Setiawan ◽  
Lediyantje Lintjewas
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Fourier Transform Infrared Spectroscopy ◽  
Hydrothermal Treatment ◽  
Energy Dispersive ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

Magnesite (MgCO3) is the main source for production of magnesium and its compound. In Indonesia, magnesite is quite rare and can be only found in limited amount in Padamarang Island, Southeast Sulawesi Provence. Thus the properties of magnesite and the reactivity degree of the obtained product are of technological importance. The aim of this work was to analyze the characteristics of Padamarang magnesite under calcination and hydrothermal treatment processes. The processes were carried out at various temperatures with range of 150-900°C for 30 minutes. The solids were characterized with respect to their chemical and physical properties by using scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX), Fourier-transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). SEM image indicates that magnesite was formed from thin and flat hexagon sheets. The FTIR and XRD analysis disclose that MgO formed at temperature above 300°C, where as the magnesite sample also lost its mass around 50%. These results demonstrate that Padamarang magnesite decomposes to magnesium oxide and carbon dioxide at high temperature.Magnesit (MgCO3) merupakan sumber utama untuk produksi magnesium dan senyawa-senyawanya. Di Indonesia, magnesit cukup jarang dan hanya dapat ditemukan dalam jumlah yang terbatas di Pulau Padamarang, Propinsi Sulawesi Tenggara. Oleh karena itu sifat magnesit dan derajat reaktivitas dari produk-produk magnesit penting untuk diketahui. Penelitian ini bertujuan untuk menganalisis karakteristik magnesit Padamarang dengan perlakuan kalsinasi dan hidrothermal.  Proses dilakukan pada temperatur yang bervariasi dari 150-900°C selama 30 menit. Sifat kimia dan fisika dari magnesit dikarakterisasi dengan menggunakan scanning electron microscopy dengan energy-dispersive X-ray spectroscopy (SEM-EDX), Fourier-transform infrared spectroscopy (FTIR), dan X-ray diffraction (XRD). Gambar dari analisis SEM menunjukkan bahwa magnesit terbentuk dari lembaran-lembaran heksagonal yang tipis dan datar. Hasil analisis dengan FTIR dan XRD menunjukkan bahwa MgO terbentuk pada temperatur diatas 300°C, dimana sampel magnesit juga kehilangan massanya sekitar 50% pada suhu tersebut. Hal ini menunjukkan bahwa Magnesit Padamarang terdekomposisi menjadi magnesium oksida dan karbon dioksida pada temperatur tinggi.

Preparation and Characterization of Lizardite

2014 ◽  
Vol 556-562 ◽  
pp. 109-112
Author(s):  
Shu Min Zheng ◽  
Kai Ming Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Fourier Transform Infrared Spectroscopy ◽  
Hydrothermal Reaction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

Lizardite were synthesized by hydrothermal reaction in an Fe3+doped solution/environment using nanometer SiO2and MgO as precursors. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), fourier transform infrared spectroscopy (FTIR). The results show that: the synthetic samples are lizardite with a thickness ranging from 60 nm to 200 nm in the temperature range 200°C~230°C.

scholarly journals Highly ordered polyaniline as an efficient dye remover

2017 ◽  
Vol 36 (1-2) ◽  
pp. 429-440 ◽  
Author(s):  
Pinki Chakraborty ◽  
Aman Kothari ◽  
Rajamani Nagarajan
Keyword(s):  
Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Diffraction Pattern ◽  
Fourier Transform Infrared Spectroscopy ◽  
Room Temperature ◽  
Fourier Transform Infrared ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

Polyaniline was synthesized by the chemical oxidative polymerization procedure at room temperature employing hydrogen peroxide (H2O2) as oxidant and ferrous chloride (FeCl2·2H2O) and vanadyl sulphate (VOSO4·H2O) as co-catalysts, respectively. The obtained polymers were characterized by high resolution powder X-ray diffraction, Fourier transform infrared spectroscopy, Raman, UV–Visible, photoluminescence spectroscopy, thermogravimetric Field Emission Scanning Electron Microscopy (FESEM) and Transmission Electron Microscopy (TEM) techniques. Ordered arrangement indicative of semi-crystalline nature of polyaniline was evidenced from the presence of intense reflection at d = 13.72 Å in the powder X-ray diffraction pattern followed by two lesser intense peaks at 4.61 and 3.47 Å. Fourier transform infrared spectroscopy and Raman spectroscopic results indicated the polyaniline to be emeraldine salt form. Fibrous morphology was observed in scanning electron microscope images. Nearly 93% of Methyl Orange dye was adsorbed in 30 min by the ordered polyaniline at room temperature. No significant difference in the crystallinity and/or ordering was noticed in the powder X-ray diffraction pattern after dye adsorption. The correlation between the ordered structure of polyaniline and its higher adsorption property derived in the current study has the potential to fabricate devices consisting polyaniline to detect dye molecules.

Research of Rough Structure of Superhydrophobic Film

2011 ◽  
Vol 287-290 ◽  
pp. 253-256
Author(s):  
Zhan Shen Zheng ◽  
Rui Jiao Li ◽  
Pei Qi Yan ◽  
Rong Yang ◽  
Peng Li
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Fourier Transform Infrared Spectroscopy ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Different Temperatures ◽  
Scanning Electron

Superhydrophobic film was fabricated mainly by ethyl silicate (TEOS) and ethanol (EtOH) using sol-gel method. SiO2 gel and samples coated with SiO2 sol were calcined at different temperatures, and their morphology and composition were studied using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). The results indicate that increasing calcining temperature appropriately improved the bond of nanoparticles of film successfully. Furthermore, there were only amorphous SiO2 and hydroxyl existing in the calcined film which would be benefit for the further modification.

Preparation of PVA/ Sm(NO3)3-Sm2O3 Composites Nanofibers by Electrospinning Technique

2010 ◽  
Vol 71 ◽  
pp. 22-27 ◽  
Author(s):  
Patrizia Frontera ◽  
Concetta Busacca ◽  
Vincenza Modafferi ◽  
Pierluigi Antonucci ◽  
Massimiliano Lo Faro
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Thermogravimetric Analysis ◽  
Fourier Transform Infrared Spectroscopy ◽  
X Ray Diffraction ◽  
Electrospinning Technique ◽  
X Ray ◽  
Scanning Electron

. In this work PVA/Sm2O3 composite fibers and Sm2O3 fibers (PVA and Sm(NO3)3 were used as precursors) were prepared by using electrospinning technique. The fibers obtained were characterized by scanning electron microscopy, X-ray diffraction, thermogravimetric analysis and Fourier transform infrared spectroscopy.

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.

Preparation of Borosilicate Xerogel and Research on its Mineralization

2012 ◽  
Vol 476-478 ◽  
pp. 2059-2062
Author(s):  
Chen Wang ◽  
Ya Dong Li ◽  
Gu Qiao Ding
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Ph Value ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Compositional Changes ◽  
Scanning Electron

Tributyl borate was first adopted for the introduction of boron in the preparation of bioactive borosilicate xerogel by sol-gel method. The xerogel reacted continuously in 0.25M K2HPO4 solution with a starting pH value of 7.0 at 37 °C for 1day. The structural, morphologies and compositional changes resulting from the conversion were characterized using X-ray diffraction, scanning electron microscopy and Fourier transform infrared spectroscopy. The results indicated that speed of formation of HA was cut way back on the time with the addition of boron and the induction period for the HA nucleation on the surface of the borosilicate xerogel was short than 1 days. The conversion mechanism of the borosilicate xerogels to hydroxyapaptite was also discussed.

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