The Nitric Acid Method for Protein Estimation in Biological Samples

Author(s):  
Scott A. Boerner ◽  
Crescent R. Isham ◽  
Yean Kit Lee ◽  
Jennifer D. Tibodeau ◽  
Scott H. Kaufmann ◽  
...  
2003 ◽  
pp. 31-40 ◽  
Author(s):  
Scott A. Boerner ◽  
Yean Kit Lee ◽  
Scott H. Kaufmann ◽  
Keith C. Bible

1999 ◽  
Vol 267 (1) ◽  
pp. 217-221 ◽  
Author(s):  
Keith C. Bible ◽  
Scott A. Boerner ◽  
Scott H. Kaufmann

1947 ◽  
Vol 20 (1) ◽  
pp. 315-319 ◽  
Author(s):  
J. F. Morley ◽  
J. R. Scott

Abstract From the experiments described, it appears that neither the bromine method nor the nitric acid method is perfectly satisfactory, for the following reasons. (1) Neither method gives the true free sulfur in rubbers containing sulfur-bearing accelerators, as these cause positive errors of anything up to 0.2–0.3 per cent. (2) The nitric acid method does not give the true free sulfur in rubbers, without sulfur-bearing accelerators, because the result includes some of the sulfur combined with the rubber “resins” the tests do not show definitely whether this applies also to the bromine method. (3) Neither method gives the total sulfur in the acetone extract, since some of the sulfur combined with the “resins” is not included in the result; the presence of certain sulfur-bearing accelerators increases the error. The statement previously referred to (loc. cit.), that the bromine method approximates more nearly to the elementary sulfur content and the nitric acid method more nearly to the total sulfur content of the extract, appears to be a correct generalization. In most cases, however, the difference between the results obtained by the two methods would be less than 0.1 per cent. In respect of simplicity and rapidity of working, the bromine method has the advantage over the nitric acid method, and therefore in all ordinary circumstances is the one to be recommended.


1986 ◽  
Vol 32 (8) ◽  
pp. 1464-1467 ◽  
Author(s):  
Y Tamari ◽  
S Ohmori ◽  
K Hiraki

Abstract For fluorometry of selenium in human blood, hair, and liver and in leaves, we wet-ashed the samples with conventional nitric and perchloric acids, and then extracted piazselenol (complex of Se and 2,3-diaminonaphthalene) in cyclohexane. Selenium was back-extracted from the cyclohexane into nitric acid to remove the fluorometric interferences of trace amounts of organic compounds. This fluorometric method is rapid and suitable for routine analysis. We applied the method to human hair samples and compared it with the data for non-destructive neutron activation analysis of the hair.


2000 ◽  
Vol 22 (6) ◽  
pp. 993-1002 ◽  
Author(s):  
Janez Ščančar ◽  
Radmila Milačič ◽  
Ingrid Falnoga ◽  
Maja Čemažar ◽  
Peter Bukovec

1970 ◽  
Vol 53 (6) ◽  
pp. 1172-1175 ◽  
Author(s):  
M T Jeffus ◽  
J S Elkins ◽  
C T Kenner

Abstract Mercury in biological samples is determined by digestion in nitric acid, sulfuric acid, and permanganate, followed by reduction and aeration for measurement by atomic absorption at room temperature. The average recovery is 95.8% with a standard deviation of 13.3%. The standard deviation, calculated from the difference between duplicates of 23 samples, is 0.063 μg mercury, which represents 9.4% of the average value of the samples. The method is simple and requires approximately 4 hr for completion. Mercury can be confirmed by adsorption on gold foil after maximum absorbance has been obtained during aeration.


2015 ◽  
Vol 17 (3) ◽  
pp. 1884-1892 ◽  
Author(s):  
Guoqiang Zou ◽  
Wenzhou Zhong ◽  
Liqiu Mao ◽  
Qiong Xu ◽  
Jiafu Xiao ◽  
...  

A novel hollow-structured Mn/TS-1 catalyst has been reported as a non-nitric acid route for adipic acid production from oxidative cleavage of cyclohexanone.


1941 ◽  
Vol 14 (1) ◽  
pp. 241-248 ◽  
Author(s):  
J. B. Roberts

Abstract A simple, accurate method for the determination of free carbon in either raw or vulcanized rubber is presented. It has replaced the nitric acid method entirely in the laboratory of the United States Rubber Company, Detroit, Michigan. A study of the effects of interfering substances, and numerous comparisons of results by the cresol and the nitric acid methods, are given. Results by the cresol method, in the absence of interfering substances, are within 1 per cent of the calculated free carbon content. The method requires only simple apparatus readily available.


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