Quantitative determination of nitrogen content in plant tissue by a colorimetric method

1999 ◽  
Vol 30 (13-14) ◽  
pp. 1997-2005 ◽  
Author(s):  
Bibiana Bilbao ◽  
Diego Giraldo ◽  
Patricio Hevia
2018 ◽  
Vol 10 (1) ◽  
pp. 76-83 ◽  
Author(s):  
Xue Jiao ◽  
Wanyi Liu ◽  
Di Wu ◽  
Wenhao Liu ◽  
Hongjie Song

Ultra-small nanoparticles of Mo-doped ceria (Mo/CeO2 NPs) possess enhanced peroxidase-like catalytic activity and these enzyme mimics are used here for the successful quantitative determination of blood glucose via a colorimetric method.


2017 ◽  
Vol 9 (21) ◽  
pp. 3151-3158 ◽  
Author(s):  
Thangarasu Sasikumar ◽  
Malaichamy Ilanchelian

In this work, we have developed a simple, rapid, sensitive and selective colorimetric method for the quantitative determination of hypochlorite (ClO−) ions by using triangular silver nanoprisms (AgNPRs) as a colorimetric probe.


1968 ◽  
Vol 51 (3) ◽  
pp. 540-543
Author(s):  
John Wiskerchen

Abstract A colorimetric method for the quantitative determination of sodium lauryl sulfate in liquid, frozen, and powdered egg white was studied by eight collaborators. Determinations were made on flake and powdered egg white at levels of 0.05, 0.1, and 0.2% (w/w) and on liquid egg white at levels of 0.006, 0.0125, and 0.0250% (w/w) sodium lauryl sulfate. The egg white is dissolved in water, and the protein is precipitated with ethanol and removed by filtration. An aliquot of the filtrate is evaporated to dryness, and the residue is dissolved in water and acidified with sulfuric acid. The sodium lauryl sulfate is complexed with Azure A, extracted into chloroform, and determined spectrophotometrically at 637 mμ. A blank determination is made on another aliquot of the filtrate by complexing the sodium lauryl sulfate with benzethonium chloride. This is a stable colorless complex. Average recoveries in the collaborative study were 98—102% with a mean deviation of 2.8—5.4%. It is recommended that the method be adopted as official, first action.


1968 ◽  
Vol 109 (1) ◽  
pp. 13-18 ◽  
Author(s):  
D. E. S. Stewart-Tull

A colorimetric method is described whereby the direct quantitative determination of glucosamine, galactosamine and muramic acid can be achieved without previous treatment of the cell-wall hydrolysate, for example by column chromatography. Molar ratios of hexosamines in cell-wall preparations, from a number of bacterial species, determined by this method were found to be in general agreement with previously published results.


1966 ◽  
Vol 17 (3) ◽  
pp. 513-520 ◽  
Author(s):  
Guido G. Guidotti ◽  
Angelo F. Borghetti ◽  
Lodovico Loreti

1979 ◽  
Vol 15 (1) ◽  
pp. 67-73 ◽  
Author(s):  
Christopher S. Frings ◽  
Joseph M. Saloom

1977 ◽  
Vol 23 (5) ◽  
pp. 811-812 ◽  
Author(s):  
H Yatzidis

Abstract Total urinary protein is rapidly precipitated at room temperature by tannic acid. The tannic acid/protein precipitate, dissolved in aqueous triethanolamine/ferric chloride solution, gives a purple-violet color of high absorptivity. Absorbance at 510 nm is linearly related to concentration from 0.05 to 1.50 A for a protein content of 0.05 to 1.50 g/liter, and less than 5 mg/liter can be detected. The CV and analytical recovery ranged from 0.5 to 1.8% and 98 to 103%, respectively. Nonprotein urinary constituents do not interfere.


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