Characterization of Bismuth Vanadate Nanopowder Prepared by Microwave Method

2016 ◽  
Vol 872 ◽  
pp. 253-257 ◽  
Author(s):  
Pusit Pookmanee ◽  
Prakasit Intaphong ◽  
Jitrephan Phanmalee ◽  
Wiyong Kangwansupamonkon ◽  
Sukon Phanichphant
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Bismuth Vanadate ◽  
Microwave Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ammonium Vanadate ◽  
Scanning Electron

Bismuth vanadate (Bi2VO5.5) nanopowder was prepared by microwave method at 500 Watt for 2, 4 and 6 min. Bismuth nitrate pentahydrate (Bi (NO3)3•5H2O) and ammonium vanadate (NH4VO3) were used as the starting precursors with mole ratio of 2:1. The phase of Bi2VO5.5 nanopowder was characterized by X-ray diffraction (XRD). The morphology of Bi2VO5.5 nanopowder was investigated by scanning electron microscopy (SEM). The chemical composition of Bi2VO5.5 nanopowder was determined by energy dispersive X-ray spectroscopy (EDXS). The functional groups of Bi2VO5.5 nanopowder was identified by fourier transform infrared spectroscopy (FTIR).

Synthesis and Characterization of NiO Doped SnO2 Nano-Flowers

2013 ◽  
Vol 575-576 ◽  
pp. 58-60
Author(s):  
Wei Ping Tang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectrum ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Hydrothermal Route ◽  
X Ray ◽  
Scanning Electron

In this present work, a new method for preparing NiO doped SnO2 nanoflowers by hydrothermal route is suggested. The composition and microstructure of samples were characterized by field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD) and Fourier transform infrared spectrum (FTIR). Moreover, a possible formation mechanism was discussed.

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.

Intercalation of Tb(III) into magadiite and characterization of Tb-intercalated magadiites

Clay Minerals ◽  
2016 ◽  
Vol 51 (4) ◽  
pp. 697-706 ◽  
Author(s):  
Yufeng Chen ◽  
Bao Yao ◽  
Yan Zou ◽  
Yudong Yan
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Ion Exchange ◽  
Basal Spacing ◽  
X Ray Diffraction ◽  
X Ray ◽  
Differential Thermogravimetry ◽  
Scanning Electron

AbstractThe intercalation of Tb(III) into layered magadiite is achieved by three-step ion exchanges with H+/Na+, TBA+ (tetra-n-butylammonium ions)/H+ and Tb(EDTA)3+/TBA+. Various techniques, including powder X-ray diffraction (XRD), scanning electron microscopy equipped with energy dispersive X-ray (SEM-EDX), thermogravimetric and differential thermogravimetry (TG-DTG), Fourier transform infrared (FTIR) spectroscopy, and photoluminescent spectroscopy (PL), were employed to characterize the Tb-intercalated magadiites. The XRD results revealed that the basal spacing of the Tb-intercalated magadiites was obviously larger than that of the Na-magadiite, confirming the intercalation. The IR spectra showed no bands attributable to EDTA in the Tb-intercalated magadiites, indicating that the EDTA has broken away from Tb(III)-ETDA complexes during ion exchange. Moreover, the basal spacing of Tb-intercalated magadiite tends to increase slightly with the increase in water content in the Tb-intercalated magadiite. The PL spectra show weak emissions, attributed to 5D4-7FJ (J = 3, 4, 5, 6) transitions of Tb3+.

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.

Preliminary Preparation and Characterization Studies of Cellulose from Merbau (Intsia bijuga)

2012 ◽  
Vol 620 ◽  
pp. 314-319
Author(s):  
Nur Amira Mamat Razali ◽  
Fauziah Abdul Aziz ◽  
Saadah Abdul Rahman
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Alkaline Treatment ◽  
Raw Material ◽  
X Ray Diffraction ◽  
X Ray ◽  
Preliminary Preparation ◽  
Characterization Studies ◽  
Scanning Electron

Hardwood is wood from angiosperm trees. The characteristic of hardwood include flowers, endosperm within seeds and the production of fruits that contain the seeds. This paper aims to discuss the preparation and characterization of cellulose obtained from hardwood. The hardwood Merbau (Intsia bijuga) was chosen as raw material in this study. Alkaline treatment and delignification methods were used for the preparation of cellulose. Acid hydrolysis was employed to produce cellulose nanocrystal (CNC). The treated and untreated samples were characterized using x-ray diffraction (XRD) and field emission scanning electron microscopy (FE-SEM). The final product, from both trated and untreated samples were then compared.

Hydrothermal Synthesis and Characterization of BiFeO3 Polyhedral Crystallites

2012 ◽  
Vol 174-177 ◽  
pp. 508-511
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Yu Jiang Wang ◽  
Xiao Feng Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

BiFeO3 polyhedrons had been successfully synthesized via a hydrothermal method. The as-prepared products were characterized by power X-ray diffraction (XRD) pattern, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The possible mechanisms for the formation of BiFeO3 polyhedrons were discussed. Though comparison experiments, it was found that the kind of precursor played a key role on the morphology control of BiFeO3 crystals.

Characterization of a coating for radioprotection, by X-ray diffraction, scanning electron microscopy, and dispersive energy spectroscopy

2022 ◽  
Vol 321 ◽  
pp. 126326
Author(s):  
Gladis Aparecida Galindo Reisemberger de Souza ◽  
Ramón Sigifredo Cortés Paredes ◽  
Frieda Saicla Barros ◽  
Gustavo Bavaresco Sucharski ◽  
Sebastião Ribeiro Junior ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

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.

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.

Sign in / Sign up

Export Citation Format

Share Document