Author(s):  
Pratibha L. Gai ◽  
M. A. Saltzberg ◽  
L.G. Hanna ◽  
S.C. Winchester

Silica based ceramics are some of the most fundamental in crystal chemistry. The cristobalite form of silica has two modifications, α (low temperature, tetragonal form) and β (high temperature, cubic form). This paper describes our structural studies of unusual chemically stabilized cristobalite (CSC) material, a room temperature silica-based ceramic containing small amounts of dopants, prepared by a wet chemical route. It displays many of the structural charatcteristics of the high temperature β-cristobalite (∼270°C), but does not undergo phase inversion to α-cristobalite upon cooling. The Structure of α-cristobalite is well established, but that of β is not yet fully understood.Compositions with varying Ca/Al ratio and substitutions in cristobalite were prepared in the series, CaO:Al2O3:SiO2 : 3-x: x : 40, with x= 0-3. For CSC, a clear sol was prepared from Du Pont colloidal silica, Ludox AS-40®, aluminium nitrate nonahydrate, and calcium nitrate hexahydrate in proportions to form a final composition 1:2:40 composition.


2013 ◽  
Vol 770 ◽  
pp. 68-71 ◽  
Author(s):  
Supphadate Sujinnapram ◽  
Uraiphorn Termsuk ◽  
Atcharawan Charoentam ◽  
Sutthipoj Sutthana

The nanocrystalline ZnO powders were synthesized by a direct thermal decomposition using zinc nitrate hexahydrate as starting materials. The precursor was characterized by TG-DTA to determine the thermal decomposition and crystallization temperature which was found to be at 325 oC. The precursors were calcined at different temperatures of 400, 500, and 600°C for 4 h. The structure of the prepared samples was studied by XRD, confirming the formation of wurtzite structure. The synthesized powders exhibited the UV absorption below 400 nm (3.10 eV) with a well defined absorption peak at around 285 nm (4.35 eV). The estimated direct bandgaps were obtained to be 3.19, 3.16, and 3.14 eV for the ZnO samples thermally decomposed at 400, 500, and 600°C, respectively.


Author(s):  
Gage P. Ashton ◽  
Edward L. Charsley ◽  
Lindsay P. Harding ◽  
Gareth M. B. Parkes

AbstractA simultaneous DSC–thermomicroscopy system (DSC450 Linkam Scientific) was applied to the study of phase transitions in rubidium nitrate and silver iodide, the oxidation of polyethylene, the thermal degradation of polylactic acid and magnesium nitrate hexahydrate, and the reversible transitions in thermochromic inks. The results demonstrated the benefits of obtaining simultaneous optical data, both images and light intensity measurements, with DSC, particularly in the interpretation of complex processes and the detection of events with small changes in enthalpy.


2010 ◽  
Vol 658 ◽  
pp. 29-32 ◽  
Author(s):  
Kanit Soongprasit ◽  
Duangdao Aht-Ong ◽  
Viboon Sricharoenchaikul ◽  
Duangduen Atong

. La1-xCexCoO3 (x=0, 0.2, and 0.4) perovskite-type mixed oxides using polyvinyl alcohol (PVA) as complexing agent at two molar ratio of metal ion to PVA (1:1 and 1:2) were successfully prepared by sol-gel process. The precursor included lanthanum (II) nitrate hexahydrate, cerium (II) nitrate hexahydrate, and cobalt (II) nitrate hexahydrate where polyvinyl alcohol was added as complexing agent. The suitable condition of Cerium (Ce) substitution and PVA molar ratio were established for further application in hydrocarbon conversion to high value added products. TGA thermogram of as-prepared precursor showed that PVA absolutely decomposed at temperature higher than 500°C. XRD patterns of calcined catalyst showed both LaCoO3 rhombohedral and CeO2 cubic structures that confirmed the formation of mixed crystal structure. Nevertheless, Co3O4 slightly appeared with low peak intensity which came from the oxidation reaction of as-prepared catalyst during calcinations. XRD showed that PVA did not effect to crystal structure of synthesized catalyst. Higher PVA content added in the precursor cause the reduction of crystal growth of catalyst in calcinations step. In contrast, morphology of catalyst is directly related with PVA content such that the spongy and sheet-like structure were formed with increasing PVA content which prevented the agglomeration of particles. The results showed that PVA content play an important role in morphology of perovskite-type mixed oxide catalysts but did not affected to their crystal structures.


2011 ◽  
Vol 312-315 ◽  
pp. 1044-1048
Author(s):  
Salina Muhamad ◽  
Abu Bakar Suriani ◽  
Mohamad Zainizan Sahdan ◽  
Anuar Ahmad ◽  
Yosri M. Siran ◽  
...  

In this paper, the study of supergrowth VACNTs after being immersed in zinc oxide solution were presented. Vertically aligned carbon nanotubes (VACNTs) were first deposited on silicon with the orientation of [1 0 0] before being immersed in an aqueous solution of zinc nitrate hexahydrate and hexamethylenetetramine. Physical changes have been observed by scanning electron microscopy, SEM in the VACNTs, where the significant expansion of length of up to almost 0.8 mm was achieved after the immersion of 4.5 hr. The supergrowth of VACNTs was observed and analyzed by energy dispersive x-ray spectroscopy, EDX to substantiate the incorporation of CNTs and ZnO of the sample. Raman spectroscopy and x-ray diffraction, XRD were used to inspect the crystal orientation to support our findings.


Author(s):  
Hanh

In this work, ZnO nanorods (NRs) were successfully grown on printed circuit board substrates (PCBs) by utilizing a one-step, seedless, low-cost hydrothermal method. It was shown that by implementing a galvanic cell structure in an aqueous solution of 80 mM of zinc nitrate hexahydrate and hexamethylenetetramine, ZnO NRs can directly grow on the PCBs substrate without the assistance of a seed layer. The effect of hydrothermal time on the surface morphologies, and the crystallinity of the as-grown ZnO nanorods (NRs) was also investigated. The as-grown ZnO NRs also exhibited a significant enhancement in vertical growth and their crystallinity with 5 hour growth.


2018 ◽  
Vol 2018 ◽  
pp. 1-9 ◽  
Author(s):  
D. A. R. Souza ◽  
M. Gusatti ◽  
R. Z. Ternus ◽  
M. A. Fiori ◽  
H. G. Riella

A practical and economical method was developed for the production of an antibacterial cotton fabric using zinc oxide nanostructures without the use of surface modifying agents. In this process, zinc nitrate hexahydrate and potassium hydroxide were used as starting materials and the reaction was performed at 50°C. The in situ growth of ZnO nanostructures on cotton fabric occurred in a single-stage process, and it started when the fabric samples were dipped for 1 min in the solution containing all the starting materials. The treated and untreated fabric samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), and EDS. The cotton fabrics coated with ZnO nanostructures presented an antibacterial efficiency towards Pseudomonas aeruginosa, a gram-negative bacteria, and Staphylococcus aureus (S. aureus), a gram-positive bacteria.


Sign in / Sign up

Export Citation Format

Share Document