scholarly journals The effect of CaCO3 addition on the crystallization behavior of ZnO crystal glaze fired at different gloss firing and crystallization temperatures

2010 ◽  
Vol 42 (3) ◽  
pp. 345-355 ◽  
Author(s):  
A.R. Jamaludin ◽  
S.R. Kasim ◽  
Z.A. Ahmad
Keyword(s):  
Electron Microscope ◽  
Crystallization Temperature ◽  
Crystallization Behavior ◽  
Isothermal Holding ◽  
Sem Analysis ◽  
Ceramic Product ◽  
X Ray ◽  
Glazed Ceramic ◽  
Zno Crystal ◽  
Scanning Electron

A glazed ceramic product with crystalline structure gives an artistic effect. In this study, the effects of calcium carbonate (CaCO3) addition into glaze batches on the crystallization behavior of crystal glaze were studied. Samples were fired at different gloss firing temperatures ranging from 1000-1200?C with 1060?C crystallization temperature. Xray diffraction (XRD) and energy dispersive X-ray spectrometer (EDX) analysis of the phases identified these crystals as willemite (Zn2SiO4) in the form of spherulites. Scanning electron microscope (SEM) analysis indicated that willemite crystals are in the acicular needle like shape. XRD result showed that the intensities of crystal peaks decreased with the addition of CaCO3 up to 3.0 wt%. However, there was no willemite crystals formation as the amount of CaCO3 raised to 5.0 wt%. Besides that, the results also indicated that willemite growth occurs during isothermal holding at crystallization temperature instead of during cooling from gloss firing temperature.

The Effect of CaCO3 Addition on Physical Properties of ZnO-Based Crystal Glaze

2012 ◽  
Vol 620 ◽  
pp. 12-16 ◽  
Author(s):  
Abdul Rashid Jamaludin ◽  
Shah Rizal Kasim ◽  
Zainal Arifin Ahmad
Keyword(s):  
Electron Microscope ◽  
Calcium Carbonate ◽  
Scanning Electron Microscope ◽  
Physical Properties ◽  
Crystallization Temperature ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

The effects of calcium carbonate (CaCO3) addition on the physical properties of ZnO-based crystal glaze batches were investigated. Samples were fired at different gloss firing temperatures ranging from 1180-1220°C with 3 hours soaking at 1060°C crystallization temperature. X-ray diffraction (XRD) analysis identifiedthe crystal phase occurred as willemite (Zn2SiO4) and the scanning electron microscope (SEM) analysis indicated that willemite crystals are in the acicular needle like shape that formed spherulite. The intensities of willemite peaks decreased with CaCO3 addition and completely vanished at 5.0 wt% CaCO3. Varied formation of spherulites developed of the surface of crystal glaze as the flows of the glaze stretched further as the amount of CaCO3 increased.

scholarly journals Characterization of Fe Doped AC/TiO2

2019 ◽  
Vol 8 (12S) ◽  
pp. 1146-1147
Keyword(s):  
Activated Carbon ◽  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
Anatase Phase ◽  
Sol Gel ◽  
Sem Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

Abstract: The photocatalytic composite Fe doped AC/TiO2 has been prepared by sol-gel method. The prepared Fe doped AC/TiO2 composite were characterized by scanning electron microscope (SEM) and X-ray diffraction (XRD).The SEM analysis showed that Fe and TiO2 were attached to the Activated Carbon surfaces. The X-Ray Diffraction data showed that Fe doped AC/TiO2 composite mostly contained anatase phase.

scholarly journals Improvement of Physical Properties of Viscose Using Nano GeO2 as Doping Material

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Hamed Daneshian ◽  
Shahnaz Nayebzadeh ◽  
Abolfazl Davodiroknabadi
Keyword(s):  
Thermal Properties ◽  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
Crystallization Temperature ◽  
Germanium Dioxide ◽  
Elemental Mapping ◽  
X Ray ◽  
As Doping ◽  
Mapping Analysis ◽  
Scanning Electron

Abstract The properties of viscose\TiO2 and viscose\TiO2\germanium dioxide (GeO2) are investigated and compared. The elemental mapping analysis using a field emission scanning electron microscope (FESEM) shows the excellent distribution of nanomaterials, while the energy dispersive X-ray (EDX) confirms its existence. The 500 s cycle of rubbing test indicates that the abrasion resistance of treated samples improves significantly. In addition, the doping of nano GeO2 enhances the strength of the treated samples. Furthermore, the thermal behavior of the treated samples, characterized by differential scanning calorimeter (DSC), results in a higher crystallization temperature and doping GeO2 increases the thermal properties of viscose in comparison with nano TiO2. The study of ultraviolet blocking indicates that doping GeO2 can improve the transmission of ultraviolet even from TiO2.

CuO Microspheres Synthesized via the Easy Hydrothermal Method

2012 ◽  
Vol 159 ◽  
pp. 84-87
Author(s):  
Xiao Ming Fu
Keyword(s):  
Electron Microscope ◽  
Reaction Time ◽  
Scanning Electron Microscope ◽  
Hydrothermal Method ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Cuo Microspheres ◽  
Scanning Electron

CuO microspheres are successfully synthesized with CuCl2 as copper source and Na2CO3 as auxiliary salt at 240 °C for 24 h via the easy hydrothermal method. The phase and the morphologies of the samples have been characterized and analyzed by XRD (X-ray diffraction) and SEM (Scanning electron microscope), respectively. XRD analysis shows that the phase of as obtained samples is CuO. SEM analysis confirms that the increase of the reaction time, the reaction temperature and the auxiliary salt is propitious to synthesize CuO microspheres.

Synthesis of CuO Flower-Nanostructure via the Hydrothermal Method

2013 ◽  
Vol 873 ◽  
pp. 131-134
Author(s):  
Xiao Ming Fu ◽  
Jie Ren
Keyword(s):  
Electron Microscope ◽  
Reaction Time ◽  
Scanning Electron Microscope ◽  
Hydrothermal Method ◽  
Reaction Temperature ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

CuO flower-nanostructures are successfully synthesized with CuCl2 as copper source and Na2CO3 as auxiliary salt at 180 °C for 24 h via the simple hydrothermal method. The phase and the morphologies of the samples have been characterized and analyzed by XRD (X-ray diffraction) and SEM (Scanning electron microscope), respectively. XRD analysis shows that the phase of as obtained samples is CuO. SEM analysis confirms that the increase of the reaction temperature is propitious to synthesize CuO flower-nanostructures while the increase of the reaction time is not in favor of their synthesis. The influence of the increase of the auxiliary salt on the morphology of CuO flower-nanostructures is not remarkable. The mechanism of the formation of CuO flower-nanostructure is discussed.

The Influence of the Hydrothermal Temperature on the Morphologies of β-Ni(OH)2 Nanospheres and Nanoflakes

2012 ◽  
Vol 159 ◽  
pp. 376-379 ◽  
Author(s):  
Xiao Ming Fu
Keyword(s):  
Electron Microscope ◽  
High Temperature ◽  
Scanning Electron Microscope ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
X Ray Diffraction ◽  
Hydrothermal Temperature ◽  
X Ray ◽  
Low Reaction Temperature ◽  
Scanning Electron

β-Ni(OH)2 nanospheres and nanoflakes have been successfully synthesized with nickel nitrate as nickel source and stronger ammonia water as precipitant via the hydrothermal method. The phase and the morphologies of the samples have been characterized and analyzed by XRD (X-ray diffraction) and SEM (Scanning electron microscope), respectively. XRD analysis shows that the phase of the samples is β-Ni(OH)2. SEM analysis confirms that the low reaction temperature is propitious to the synthesis of β-Ni(OH)2 nanospheres. However, The high temperature is in favor of the synthesis of β-Ni(OH)2 nanosflakes.

Synthesis of Perovskite Brown Pigments

2011 ◽  
Vol 695 ◽  
pp. 303-306
Author(s):  
In Don Joo ◽  
Kyong Sop Han ◽  
Byung Ha Lee
Keyword(s):  
Particle Size ◽  
Electron Microscope ◽  
Sem Analysis ◽  
Heating Condition ◽  
X Ray Diffraction ◽  
Soaking Time ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Cie Lab ◽  
Scanning Electron

This study aims to synthesize Cr doped Perovskite brown pigments. The pigment were synthesized by doping Cr2O3(0.01 ~ 0.05mole) for TiO2(0.993 ~ 0.963 mole) at 1150 ~ 1350°C. The samples were characterized by X-ray diffraction (XRD), Raman Spectrometer, Scanning Electron Microscope(SEM) and the UV/Vis spectroscopy. The optimum composition was CaCr0.03Ti0.978O3and heating condition was 1300°C for 3h of soaking time. The doped Cr ion for Perovskite was observed to be Cr(Ⅲ) and Cr(Ⅳ). The brown color was mixed with violet doped by Cr4+(3A2 → 3T2) and Blueish-Green doped by Cr3+(4A2g → 4F1g). The results of SEM analysis showed the Perovskite structure and the particle size was approximately 2µm. The color in Frit 6060 glaze adding 10wt% pigment was Redish Brown, and CIE Lab parameters were L*= 41.53, a*=13.27 and b*=9.94 .

X-ray micro tomography in the scanning electron microscope

1978 ◽  
Vol 36 (1) ◽  
pp. 106-107 ◽  
Author(s):  
W. Brünger
Keyword(s):  
Electron Beam ◽  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
Target Surface ◽  
The Body ◽  
X Rays ◽  
Cross Sectional ◽  
X Ray ◽  
Micro Tomography ◽  
Scanning Electron

Reconstructive tomography is a new technique in diagnostic radiology for imaging cross-sectional planes of the human body /1/. A collimated beam of X-rays is scanned through a thin slice of the body and the transmitted intensity is recorded by a detector giving a linear shadow graph or projection (see fig. 1). Many of these projections at different angles are used to reconstruct the body-layer, usually with the aid of a computer. The picture element size of present tomographic scanners is approximately 1.1 mm2.Micro tomography can be realized using the very fine X-ray source generated by the focused electron beam of a scanning electron microscope (see fig. 2). The translation of the X-ray source is done by a line scan of the electron beam on a polished target surface /2/. Projections at different angles are produced by rotating the object.During the registration of a single scan the electron beam is deflected in one direction only, while both deflections are operating in the display tube.

PHAX-SCAN: Functional integration of a Scanning Electron Microscope and an energy-dispersive x-ray analyser

1989 ◽  
Vol 47 ◽  
pp. 56-57
Author(s):  
Marc H. Peeters ◽  
Max T. Otten
Keyword(s):  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
High Speed ◽  
High Performance ◽  
Functional Integration ◽  
Energy Dispersive ◽  
X Rays ◽  
X Ray ◽  
High Speed Analysis ◽  
Scanning Electron

Over the past decades, the combination of energy-dispersive analysis of X-rays and scanning electron microscopy has proved to be a powerful tool for fast and reliable elemental characterization of a large variety of specimens. The technique has evolved rapidly from a purely qualitative characterization method to a reliable quantitative way of analysis. In the last 5 years, an increasing need for automation is observed, whereby energy-dispersive analysers control the beam and stage movement of the scanning electron microscope in order to collect digital X-ray images and perform unattended point analysis over multiple locations.The Philips High-speed Analysis of X-rays system (PHAX-Scan) makes use of the high performance dual-processor structure of the EDAX PV9900 analyser and the databus structure of the Philips series 500 scanning electron microscope to provide a highly automated, user-friendly and extremely fast microanalysis system. The software that runs on the hardware described above was specifically designed to provide the ultimate attainable speed on the system.

PENGGUNAAN TiO2 PARTIKEL NANO HASIL SINTESIS BERBASIS AIR MENGGUNAKAN METODA SOL-GEL PADA BAHAN KAPAS SEBAGAI APLIKASI UNTUK TEKSTIL ANTI UV

Arena Tekstil ◽  
2013 ◽  
Vol 28 (1) ◽  
Author(s):  
Maya Komalasari ◽  
Bambang Sunendar
Keyword(s):  
Fourier Transform ◽  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
Sol Gel ◽  
Crosslinking Agent ◽  
X Ray Diffraction ◽  
Nano Tio2 ◽  
X Ray ◽  
Infra Red ◽  
Scanning Electron

Partikel nano TiO2 berbasis air dengan pH basa telah berhasil disintesis dengan menggunakan metode sol-gel dan diimobilisasi pada kain kapas dengan menggunakan kitosan sebagai zat pengikat silang. Sintesis dilakukan  dengan prekursor TiCl4 pada konsentrasi 0,3 M, 0,5 M dan 1 M, dan menggunakan templat kanji dengan proses kalsinasi pada suhu 500˚C selama 2 jam. Partikel nano TiO2 diaplikasikan ke kain kapas dengan metoda pad-dry-cure dan menggunakan kitosan sebagai crosslinking agent. Berdasarkan hasil Scanning Electron Microscope (SEM),diketahui bahwa morfologi partikel TiO2 berbentuk spherical dengan ukuran nano (kurang dari 100 nm). Karakterisasi X-Ray Diffraction (XRD) menunjukkan adanya tiga tipe struktur kristal utama, yaitu (100), (101) dan (102) dengan fasa kristal yang terbentuk adalah anatase dan rutile. Pada karakterisasi menggunakan SEM terhadap serbuk dari TiO2 yang telah diaplikasikan ke permukaan kain kapas, terlihat adanya imobilisasi partikel nano TiO2 melalui ikatan hidrogen silang dengan kitosan pada kain kapas. Hasil analisa tersebut kemudian dikonfirmasi dengan FTIR (Fourier Transform Infra Red) yang hasilnya memperlihatkan puncak serapan pada bilangan gelombang 3495 cm-1, 2546 cm-1, dan 511 cm-1,  yang masing-masing diasumsikan sebagai adanya vibrasi gugus fungsi O-H, N-H dan Ti-O-Ti. Hasil SEM menunjukkan pula bahwa kristal nano yang terbentuk diantaranya adalah fasa rutile , yang berdasarkan literatur terbukti dapatberfungsi sebagai anti UV.

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