Show/Hide Menu
Hide/Show Apps
anonymousUser
Logout
Türkçe
Türkçe
Search
Search
Login
Login
OpenMETU
OpenMETU
About
About
Açık Bilim Politikası
Açık Bilim Politikası
Frequently Asked Questions
Frequently Asked Questions
Browse
Browse
By Issue Date
By Issue Date
Authors
Authors
Titles
Titles
Subjects
Subjects
Communities & Collections
Communities & Collections
Synthesis and characterization of hydrothermally grown potassium titanate nanowires
Date
2015-06-01
Author
KAPUSUZ, Derya
Kalay, Yunus Eren
Park, Jongee
Öztürk, Abdullah
Metadata
Show full item record
This work is licensed under a
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
.
Item Usage Stats
1
views
0
downloads
Potassium titanate (KT) nanowires were synthesized by a one-step hydrothermal reaction between TiO2 and aqueous KOH solution. The effects of KOH concentration and reaction time on hydrothermal formation and KT nanowire growth were investigated. The nanowire growth mechanism was elucidated using a combined study of powder X-ray diffraction, and scanning and transmission electron microscopy. The results revealed that hydrothermal growth was initiated by the formation of amorphous-like Ti-O-K sheets in anatase. Increasing hydrothermal reaction time caused the transformation of anatase to Ti-O-K sheets, from which potassium hexa-titanate (K2Ti6O13) nuclei formed and grew to establish one-dimensional morphology through preferential growth along the b-axis. It was revealed that the hydrothermal reactions followed a quite different mechanism than the well-known calcination route. Potassium tetra-titanate (K2Ti4O9) crystals formed in the amorphous region using the hexa-titanate phase as a nucleation site for heterogeneous crystallization. Increasing the KOH concentration in the solution accelerated the hydrothermal reaction rate.
Subject Keywords
Potassium titanate
,
Hydrothermal
,
High-resolution transmittance electron microscopy (HRTEM)
URI
https://hdl.handle.net/11511/55948
Journal
JOURNAL OF CERAMIC PROCESSING RESEARCH
Collections
Department of Metallurgical and Materials Engineering, Article