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227934-46-5

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227934-46-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 227934-46-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,7,9,3 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 227934-46:
(8*2)+(7*2)+(6*7)+(5*9)+(4*3)+(3*4)+(2*4)+(1*6)=155
155 % 10 = 5
So 227934-46-5 is a valid CAS Registry Number.

227934-46-5Relevant academic research and scientific papers

Kinetics of thermal decomposition of polyfunctional substituted azido-1,2,4-triazoles

Kruglyakova,Stepanov

, (2012)

Abstract-The structural and kinetics regularities and the mechanism of the limiting step of thermal decomposition of the polyfunctional substituted 1,2,4-triazoles in the melt and in solutions of inert solvents were established. The activation parameters

Effects of Pd particle size and ceria loading on NO reduction with CO

Holles, Joseph H.,Davis, Robert J.,Murray, Thomas M.,Howe, James M.

, p. 193 - 206 (2000)

There has been significant interest in using Pd-only catalysts for automobile three-way exhaust gas conversion. Three-way converters are designed to reduce emissions of CO, NOx, and uncombusted hydrocarbons. These catalysts often contain noble metals, e.g., Pd, Pt, and Rh, with a ceria promoter supported on alumina. In view of this, the kinetics of the NO + CO reaction at 433-573 K were studied over supported palladium with and without ceria promotion. For the ceria promoted samples, the interface between ceria and palladium was changed by varying particle size and the quantity of ceria postdeposited on the Pd particles. The Pd particle size affected activity and apparent reaction orders. For the unpromoted catalyst, the Pd particle size of ~ 4-5 nm average dia had a lower turnover frequency than 1-nm size particles, indicating structure sensitivity of the NO + CO reaction. However, the ceria-promoted samples displayed a maximum in catalytic activity for 2-nm palladium. This maximum in reaction rate indicated a balance between the Pd/ceria interface that promotes NO dissociation and the Pd metal surface that catalyzes product formation. TPD results on adsorbed NO were consistent with this interpretation.

Improved low temperature NH3-SCR performance of FeMnTiOx mixed oxide with CTAB-assisted synthesis

Wu, Shiguo,Yao, Xiaojiang,Zhang, Lei,Cao, Yuan,Zou, Weixin,Li, Lulu,Ma, Kaili,Tang, Changjin,Gao, Fei,Dong, Lin

supporting information, p. 3470 - 3473 (2015/03/30)

FeMnTiOx mixed oxide is prepared by the CTAB-assisted co-precipitation method, and the transformation of anatase into rutile is inhibited by CTAB to some extent. The catalyst obtained in the present work shows nearly 100% NO conversion at 100-350 °C, more than 80% N2 selectivity at 75-200 °C, and excellent H2O durability for the selective catalytic reduction of NO by NH3 with a space velocity of 30000 mL g-1 h-1. This journal is

Mechanism of thermal decomposition of d-metals nitrates hydrates

Malecki,Gajerski,Labus,Prochowska-Klisch,Wojciechowski

, p. 17 - 23 (2008/10/08)

A series of six nitrates(V) hydrates of 4d-metals as well as mercury and cadmium thermal decomposition was examined by DTA, TG and EGA techniques. It was found that thermal decomposition of d-metals nitrate(V) hydrates proceeds in three stages: partial dehydration, oxo-nitrates and hydroxide nitrates formation and metal oxides formation. General chemical equations for all decomposition stages were proposed. It was found that dehydration of hydrated salts is accompanied by partial decomposition of nitrate(V) groups.

Kinetics and Mechanism of the Oxidation of Hydroxylamine by Iodine

Rabai, Gyula,Beck, Mihaly T.

, p. 573 - 576 (2007/10/02)

Tha rate law for the iodine oxidation of hydroxylamine in acidic aqueous solution has been determined and a plausible mechanism is suggested.The reactivity of unprotonated hydroxylamine is much higher than that of the protonated form.The reaction is autoinhibitory: the rate is inversely poportional to the first and second power of the iodide concentration due to two pre-equilibra.

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