scholarly journals The Effect of Temperature and Time of the Hydrothermal Treatment in the SBA-15 Synthesis Process on the Structure and Textural Properties and the Ability to Reduce the Evolution of Tars in Tobacco Smoking

Catalysts ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 272
Author(s):  
Nerea Juárez-Serrano ◽  
Javier Asensio ◽  
Isabel Martínez-Castellanos ◽  
Maribel Beltrán ◽  
Antonio Marcilla
Keyword(s):  
Hydrothermal Treatment ◽  
Amorphous Materials ◽  
Marked Effect ◽  
Textural Properties ◽  
Effect Of Temperature ◽  
Synthesis Process ◽  
X Ray Diffraction ◽  
Santa Barbara ◽  
X Ray ◽  
Tar Reduction

Different SBA-15 (SBA, Santa Barbara Amorphous) materials were synthetized at different temperature and time during of the hydrothermal treatment. The obtained SBA-15 were characterized by N2 adsorption isotherms, scanning electron microscopy (SEM), X-ray diffraction (DRX), and density in order to establish the influence of these variables on their properties. Mixtures of the obtained catalysts with 3R4F tobacco were prepared and smoked under the ISO 3308 conditions. Temperature of the hydrothermal treatment slightly affects the tars that evolved in the smoking process of the corresponding catalyst tobacco mixtures. Contrarily, the time of the hydrothermal treatment has a marked effect on the reductions of toxic compounds in the smoke. Developed porosity has a positive correlation with the observed tar reduction, whereas the apparent density has a negative correlation with the reduction in toxicity. Moreover, the removal of the supernatant liquors during the hydrothermal treatment does not strongly modify the properties of the materials and may represent an interesting simplification of the process.

scholarly journals Reduction of the toxicity of tobacco smoke with catalytic materials: Study of the influence of SBA-15 synthesis variables, time and temperatura of the hydrothermal treatment.

2020 ◽  
Author(s):  
Nerea Juárez-Serrano ◽  
Antonio Marcilla
Keyword(s):  
Hydrothermal Treatment ◽  
Tobacco Smoke ◽  
Tobacco Smoking ◽  
Material Properties ◽  
Textural Properties ◽  
Effect Of Temperature ◽  
Synthesis Process ◽  
Special Issue ◽  
Catalytic Materials ◽  
Engineering Department

This article is associated with the MDPI "Catalysts" journal, which belongs to a Special Issue "SBA-15 and Catalysis", "The Effect of Temperature and Time of the Hydrothermal Treatment in the SBA-15 Synthesis Process on the Structure and Textural Properties and the Ability to Reduce the Evolution of Tars in Tobacco Smoking" and the authors Juárez-Serrano, N.a; Asensio, J.ª; Martínez-Castellanos, I.ª; Beltrán, M.I.ª; and Marcilla A.*a aChemical Engineering Department. University of Alicante. Apartado 99, 03690, Alicante, Spain. *Corresponding author: [email protected]      SBA-15 synthetized at different values of time and temperature of the hydrothermal treatment were mixture with tobacco in order to determine the capacity of reduction of toxic and carcirogenic compounds on tobacco smoke. The effect of temperature is not significative but time presents a remarked effect. And a parameter not frequently studied, the aparent density, has been shown the most relevant relation with the results on smoking experimentos. Finally, the effect of reduce the supernatant liquor also has been studied and the results have shown that the material properties remain practically unchanged.

Effect of Temperature on Fe3O4 Magnetic Nanoparticles Prepared by Coprecipitation Method

2014 ◽  
Vol 900 ◽  
pp. 172-176 ◽  
Author(s):  
Ji Mei Niu ◽  
Zhi Gang Zheng
Keyword(s):  
Magnetic Nanoparticles ◽  
Coprecipitation Method ◽  
Effect Of Temperature ◽  
Vibrating Sample Magnetometer ◽  
X Ray Diffraction ◽  
X Ray ◽  
Magnetic Carriers ◽  
Average Grain Size ◽  
Or Gene ◽  
Block Temperature

The Fe3O4 magnetic nanoparticles obtained by the aqueous coprecipitation method are characterized systematically using scanning electron microscope, X-ray diffraction and vibrating sample magnetometer. These magnetic nanoparticles are spheric, dispersive, and have average grain size of 50 nm. The size and magnetic properties of Fe3O4 nanoparticles can be tuned by the reaction temperature. All samples exhibit high saturation magnetization (Ms=53.4 emu·g-1) and superparamagnetic behavior with a block temperature (TB) of 215K. These properties make such Fe3O4 magnetic nanoparticles worthy candidates for the magnetic carriers of targeted-drug or gene therapy in future.

Hydrothermal Treatment of Coprecipitated YSZ Powders

2010 ◽  
Vol 660-661 ◽  
pp. 983-988 ◽  
Author(s):  
Alexander Rodrigo Arakaki ◽  
Walter Kenji Yoshito ◽  
Valter Ussui ◽  
Dolores Ribeiro Ricci Lazar
Keyword(s):  
Surface Area ◽  
Hydrothermal Treatment ◽  
Gas Adsorption ◽  
X Ray Diffraction ◽  
Electronic Microscopy ◽  
Immersion Method ◽  
Cubic Symmetry ◽  
X Ray ◽  
Granulometric Analysis ◽  
Symmetry Surface

Zirconia stabilized with 8.5 mol% yttria (YSZ) were synthesized by coprecipitation and resulting gels were hydrothermallly treated at 200°C and 220 PSI for 4, 8 and 16 hours. Products were oven dried at 70°C for 24 hours, isostatically pressed as pellets and sintered at 1500 °C for 1 hour. Powders were characterized for surface area with N2 gas adsorption, X-ray diffraction, laser diffraction granulometric analysis and scanning and transmission electronic microscopy. Density of ceramics was measured by an immersion method based on the Archimedes principle. Results showed that powders dried at 70°C are amorphous and after treatment has tetragonal/cubic symmetry. Surface area of powders presented a significant reduction after hydrothermal treatment. Ceramics prepared from hydrothermally treated powders have higher green density but sintered pellets are less dense when compared to that made with powders calcined at 800°C for 1 hour due to the agglomerate state of powders. Solvothermal treatment is a promising procedure to enhance density.

Morphology and Crystallographic Characterization of Nickel Nanowires—Influence of Magnetic Field and Current Density During Synthesis

2014 ◽  
Vol 5 (2) ◽  
Author(s):  
Mahendran Samykano ◽  
Ram Mohan ◽  
Shyam Aravamudhan
Keyword(s):  
Magnetic Field ◽  
Current Density ◽  
Quality Data ◽  
Synthesis Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nickel Nanowires ◽  
Helium Ion ◽  
Sem Imaging

This paper presents results and discussion from a comprehensive morphological and crystallographic characterization of nickel nanowires synthesized by template-based electrodeposition method. In particular, the influence of magnetic and electric field (current density) conditions during the synthesis of nickel nanowires was studied. The structure and morphology of the synthesized nanowires were studied using Helium ion microscopy (HIM) and scanning electron microscopy (SEM) methods. The HIM provided higher quality data and resolution compared to conventional SEM imaging. The crystallographic properties of the grown nanowires were also studied using X-ray diffraction (XRD). The results clearly indicated that the morphological and crystallographic properties of synthesized nickel nanowires were strongly influenced by the applied magnetic field and current density intensity during the synthesis process.

scholarly journals PREPARATION OF NICKEL NANOWIRES AND EFFECTS OF SYNTHESIS CONDITIONS ON THEIR MORPHOLOGY

2019 ◽  
Vol 57 (3A) ◽  
pp. 21
Author(s):  
Minh Truong Xuan Nguyen ◽  
Thu Thi Minh Bui ◽  
Cuc Thi Le ◽  
Linh Huu Nguyen ◽  
Y Ngoc Pham ◽  
...  
Keyword(s):  
Synthesis Process ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray ◽  
Synthesis Conditions ◽  
Nickel Nanowires ◽  
Transmission Electron ◽  
Experimental Parameters ◽  
Polyol Medium ◽  
Nickel Nanostructures

Nickel nanostructures prepared by various methods have received considerable attentions due to their numerous applications. In this study, one-dimensional nickel nanowires (NiNWs) were synthesized by the reduction of nickel (II) chloride in polyol medium. Poly (vinylpyrrolidone) (PVP) served as the surfactant and hydrazine hydrate was used as the reductant. The effects of different experimental parameters, i.e. concentration of Ni2+, volume of N2H4, concentration of PVP and reaction temperature on the formation and morphology of NiNWs were studied. The structure, composition and surface morphology of the materials were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The results showed that the morphology as well as the diameter of NiNWs could be effectively controlled by adjusting parameters of the synthesis process.

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.

Evolution of Crystalline Phase and Morphology of the Products Formed during the Hydrothermal Synthesis of Y2O3 Powders

2011 ◽  
Vol 189-193 ◽  
pp. 1275-1279
Author(s):  
Ying Wang ◽  
Gao Yang Zhao ◽  
Li Yuan
Keyword(s):  
Electron Microscopy ◽  
Hydrothermal Treatment ◽  
Crystalline Phase ◽  
Hydrothermal Reaction ◽  
Yttrium Nitrate ◽  
Temperature Reaction ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
X Ray ◽  
Transmission Electron

The crystalline phase and morphology of the products formed during the synthesis of yttrium oxide via the hydrothermal treatment yttrium nitrate were characterized by X-ray diffraction, transmission electron microscopy and scanning electron microscopy. Products with high OH/NO3ratios are formed with the increasing of hydrothermal treatment. The crystalline phases are evolved from Y2(OH)5.14(NO3)0.86•H2O toY4O(OH)9(NO3) and finally Y(OH)3. The hydrothermal reaction conditions play an important role in the synthesis of the microstructures. Results show the particle size and final morphology of samples could be controlled by reaction temperature, reaction time, and OH-concentration. Sheets, hexagonal and needle-like Y2O3powders are obtained with the hydrothermal treatment of yittrium nitrate at 180 oC to 200oC for 2-8 hours at pH 9-13.

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