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2,6-xylidine

Known as: 2,6-dimethylaniline 
 
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
Oxidation of 2,6-dimethylaniline by electro-Fenton process in acidic solution at pH 2 was investigated. The effects of pH, Fe(2… Expand
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Highly Cited
2009
Highly Cited
2009
2,6-Dimethylaniline degradation by Fenton process has been studied in depth for the purpose of learning more about the reactions… Expand
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Highly Cited
2009
Highly Cited
2009
A new approach for promoting ferric reduction efficiency using a different electrochemical cell and the photoelectro-Fenton… Expand
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Highly Cited
2007
Highly Cited
2007
In the determination of bromate and iodate, any free bromide and iodide present was quantitatively removed by anion exchange with… Expand
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Highly Cited
2005
Highly Cited
2005
Many fungi (particularly the white rot) are well suited for treatment of a broad range of textile dye effluents due to the… Expand
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Highly Cited
2001
Highly Cited
2001
The addition of an N–H bond across a carbon–carbon double or triple bond is potentially one of the most direct and efficient… Expand
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Highly Cited
2001
Highly Cited
2001
We studied the concentration of 10 primary aromatic amines (AA), which are classified as suspected carcinogens, in indoor and… Expand
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Highly Cited
1998
Highly Cited
1998
A solid-phase microextraction (SPME) protocol was developed for the quantitative analysis of monocyclic aromatic amines from… Expand
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Highly Cited
1997
Highly Cited
1997
The reaction of dimethyl carbonate (DMC) with different primary aromatic amines has been investigated under batch conditions… Expand
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Highly Cited
1993
Highly Cited
1993
A very sensitive mass-spectrometry method has been developed for the analysis of aromatic amines in tobacco smoke and in indoor… Expand
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