DIGESTION PROCEDURES FOR SIMULTANEOUS AUTOMATED DETERMINATION OF NH4, P, K, CA AND MG IN PLANT MATERIAL

1976 ◽  
Vol 56 (4) ◽  
pp. 425-432 ◽  
Author(s):  
WM. VAN LIEROP

The efficacy of several digestion procedures for mineralizing organic matter from plant tissue was compared, and a rapid and precise method suitable for automated determination of NH4, P, K, Ca and Mg in a single digest was selected. A wet-digestion technique using hydrogen peroxide and perchloric acid as oxidative agents in a sulphuric acid medium was deemed the most advantageous among the tested procedures. Appropriate manifolds were designed to determine the sought plant constituents, present in the digests, by automated instruments. Although, recovered ammonium seemed more accurate and precise with the conventional Kjeldahl procedures, mean recovered ammonium was not significantly higher than the suggested method, when the latter was corrected for oxidized ammonium. Further, significantly larger quantities of K, Ca and Mg were recovered compared to the dry-ashing method, though the differences were small. The suggested procedure was verified with a plant-tissue standard and fortified samples. Further, it has been used to digest and analyze over 7,000 plant tissue samples and a number of manure samples without any problems. Two operators can weigh, digest and analyze 100 samples in an average working day without difficulty. An additional operator can, however, quicken the pace and double the number of daily samples.

1985 ◽  
Vol 68 (3) ◽  
pp. 499-505 ◽  
Author(s):  
Robert A Isaac ◽  
William C Johnson

Abstract Fourteen laboratories participated in a collaborative study of 6 homogeneous plant tissue samples to determine the elements P, K, Ca, Mg, Mn, Fe, Al, B, Cu, Zn, and Na by plasma emission spectroscopy. Samples were dry ashed using AOAC method 3.007(a) (13th Ed.). An NBS citrus leaf standard was prepared and a portion of the resulting solution was sent to each collaborator to evaluate sample preparation errors independent of instrument error. Coefficients of variation were better than those obtained in an earlier collaborative study on multielement analysis by spark emission spectroscopy. The plasma emission method has been adopted official first action for determination of P, K, Ca, Mg, Mn, B, Cu, and Zn in plant tissues.


1969 ◽  
Vol 52 (5) ◽  
pp. 930-932
Author(s):  
Joseph L Morrison ◽  
Glenn M George

Abstract A method is described for the determination of arsenic in poultry tissue, which is sensitive to levels of less than 0.1 ppm. Tissue samples are dry-ashed in the presence of magnesium oxide and magnesium nitrate and the arsenic is determined colorimetrically with silver diethyldithiocarbamate. Arsenic content in the tissue is determined from standard curves prepared for each tissue; this technique corrects for losses during the ashing step.


1992 ◽  
Vol 23 (17-20) ◽  
pp. 2383-2397 ◽  
Author(s):  
G. S. Banuelos ◽  
G. Cardon ◽  
T. Pflaum ◽  
S. Akohoue

1975 ◽  
Vol 58 (3) ◽  
pp. 436-440 ◽  
Author(s):  
Robert A Isaac ◽  
William C Johnson

Abstract Seven laboratories participated in a collaborative study of wet ashing of plant material with a nitric-perchloric acid mixture and dry ashing at 500°C in order to determine the elements calcium, copper, iron, magnesium, manganese, potassium, and zinc by atomic absorption spectrophotometry. Five different homogeneous leaf tissue samples were analyzed and a synthetic standard solution containing all of the elements studied was included to evaluate sample preparation errors independent of instrument errors. The results indicated that plant tissue preparation by either wet or dry ashing gave similar elemental composition results for the tissues analyzed. The wet and dry ashing techniques have been adopted as official first action.


1992 ◽  
Vol 15 (10) ◽  
pp. 2085-2108 ◽  
Author(s):  
J. Benton Jones ◽  
Arthur Wallace

1973 ◽  
Vol 56 (4) ◽  
pp. 793-797 ◽  
Author(s):  
Glenn M George ◽  
Larry J Frahm ◽  
J Patrick McDonnell

Abstract The method described for the determination of total arsenic in animal tissue is sensitive to levels of 0.1 ppm. Tissue samples are dry-ashed in the presence of magnesium oxide and magnesium nitrate and the arsenic is determined colorimetrically with silver diethyldithiocarbamate. The arsenic content in the tissue is determined from standard curves prepared for each tissue, thereby correcting for losses during the ashing step. The average recovery for 8 collaborators was 98.8% for poultry tissue and 103.4% for swine tissue with an average overall coefficient of variation of 8.31% for the entire study. This method has been adopted as official first action.


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