Direct aromatic-ring amination by aqueous ammonia with a platinum loaded titanium oxide photocatalyst

2010 ◽  
Vol 46 (46) ◽  
pp. 8854 ◽  
Author(s):  
Hayato Yuzawa ◽  
Hisao Yoshida
Keyword(s):  
Titanium Oxide ◽  
Aromatic Ring ◽  
Aqueous Ammonia

scholarly journals Anti-Markovnikov Hydroamination of Alkenes with Aqueous Ammonia by Metal-Loaded Titanium Oxide Photocatalyst

2020 ◽  
Vol 142 (29) ◽  
pp. 12708-12714 ◽  
Author(s):  
Soyeong Park ◽  
Jaeyoung Jeong ◽  
Ken-ichi Fujita ◽  
Akira Yamamoto ◽  
Hisao Yoshida
Keyword(s):  
Titanium Oxide ◽  
Aqueous Ammonia

Synthesis of oxygen-deficient blue titanium oxide by discharge plasma generated in aqueous ammonia solution

2019 ◽  
Vol 489 ◽  
pp. 255-261
Author(s):  
Yoshiteru Mizukoshi ◽  
Megumi Ohwada ◽  
Satoshi Seino ◽  
Hiroshi Horibe ◽  
Yoshimi Nishimura ◽  
...  
Keyword(s):  
Titanium Oxide ◽  
Discharge Plasma ◽  
Aqueous Ammonia ◽  
Ammonia Solution ◽  
Aqueous Ammonia Solution

Reaction Mechanism of Aromatic Ring Hydroxylation by Water over Platinum-Loaded Titanium Oxide Photocatalyst

2012 ◽  
Vol 116 (48) ◽  
pp. 25376-25387 ◽  
Author(s):  
Hayato Yuzawa ◽  
Masanori Aoki ◽  
Kazuko Otake ◽  
Tadashi Hattori ◽  
Hideaki Itoh ◽  
...  
Keyword(s):  
Reaction Mechanism ◽  
Titanium Oxide ◽  
Aromatic Ring ◽  
Ring Hydroxylation

CONJUGATED OESTROGENS. I

1963 ◽  
Vol 43 (3) ◽  
pp. 345-360 ◽  
Author(s):  
Stanley Kushinsky ◽  
Jane (Wu) Tang
Keyword(s):  
Molecular Weight ◽  
Formic Acid ◽  
Ethyl Acetate ◽  
High Molecular Weight ◽  
Secondary Amine ◽  
Aqueous Ammonia ◽  
Organic Solution ◽  
Extraneous Material

ABSTRACT A convenient and mild procedure is described in this paper whereby free and conjugated oestrogens may be extracted from urine. The extracts containing approximately 90 per cent of the oestrogens are devoid of most of the extraneous material and may be reduced in volume to less than 1/15 of that of the urine. The procedure consists of the following steps: (1) a 10 per cent (v/v) solution of a high molecular weight secondary amine (Amberlite LA-2, Rohm and Haas) in ethyl acetate is washed with formic acid and water, (2) the oestrogens in urine (acidified to pH 2 or 3 with H2SO4) are extracted with the LA-2 solution, (3) the oestrogen fraction is back-extracted from the organic solution with dilute aqueous ammonia.

Electron Holographic Nano-Characterization of Gold Catalyst at Interface

2002 ◽  
Vol 727 ◽  
Author(s):  
S. Ichikawa ◽  
T. Akita ◽  
M. Okumura ◽  
M. Haruta ◽  
K. Tanaka
Keyword(s):  
Contact Angle ◽  
Titanium Oxide ◽  
Gold Catalyst ◽  
Three Dimensional ◽  
High Resolution Electron Microscopy ◽  
Electron Holography ◽  
Gold Particles ◽  
Oxide Support ◽  
The Mean ◽  
A Charge

AbstractThe catalytic properties of nanostructured gold catalyst are known to depend on the size of the gold particles and to be activated when the size decreases to a few nanometers. We investigated the size dependence of the three-dimensional nanostructure on the mean inner potential of gold catalysts supported on titanium oxide using electron holography and high-resolution electron microscopy (HREM). The contact angle of the gold particles on the titanium oxide tended to be over 90° for gold particles with a size of over 5 nm, and below 90° for a size of below 2 nm. This decreasing change in the contact angle (morphology) acts to increase the perimeter and hence the area of the interface between the gold and titanium oxide support, which is considered to be an active site for CO oxidation. The mean inner potential of the gold particles also changed as their size decreased. The value of the inner potential of gold, which is approximately 25 V in bulk state, rose to over 40 V when the size of the gold particles was less than 2 nm. This phenomenon indicates the existence of a charge transfer at the interface between gold and titanium oxide. The 3-D structure change and the inner potential change should be attributed to the specific electronic structure at the interface, owing to both the “nano size effect” and the “hetero-interface effect.”

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