TY - JOUR
T1 - Animation of n-hexanol in supercritical water
AU - Tajima, Kiyohiko
AU - Uchida, Munehiro
AU - Minami, Kimitaka
AU - Osada, Mitsumasa
AU - Sue, Kiwamu
AU - Nonaka, Toshiyuki
AU - Hattori, Hideo
AU - Arai, Kunio
PY - 2005/12/15
Y1 - 2005/12/15
N2 - The animation of 1-n-hexanol followed by amidation was carried out in supercritical water at 380, 400, and 420 °C and water densities of 0.1, 0.3, and 0.5 g/cm3. The replacement of the hydroxyl group with the amino group was found to occur in 1-n-hexanol using ammonium acetate in supercritical water without the addition of a metal or an acid catalyst. The yield of the final product, N-n-hexylacetamide, increased by increasing the reaction temperature, water density, and the amount of ammonium acetate. The yield and the selectivity of N-n-hexylacetamide were 78.5% and 87.5%, respectively, in supercritical water at 400 °C, 0.5 g/cm3, for 10 min.
AB - The animation of 1-n-hexanol followed by amidation was carried out in supercritical water at 380, 400, and 420 °C and water densities of 0.1, 0.3, and 0.5 g/cm3. The replacement of the hydroxyl group with the amino group was found to occur in 1-n-hexanol using ammonium acetate in supercritical water without the addition of a metal or an acid catalyst. The yield of the final product, N-n-hexylacetamide, increased by increasing the reaction temperature, water density, and the amount of ammonium acetate. The yield and the selectivity of N-n-hexylacetamide were 78.5% and 87.5%, respectively, in supercritical water at 400 °C, 0.5 g/cm3, for 10 min.
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U2 - 10.1021/es051308z
DO - 10.1021/es051308z
M3 - Article
C2 - 16475358
AN - SCOPUS:29244438999
SN - 0013-936X
VL - 39
SP - 9721
EP - 9724
JO - Environmental Science & Technology
JF - Environmental Science & Technology
IS - 24
ER -