A new method for the determination of ammoniacal nitrogen in soils

1924 ◽  
Vol 14 (4) ◽  
pp. 548-554 ◽  
Author(s):  
W. McLean ◽  
G. W. Robinson
Keyword(s):  
Sodium Chloride ◽  
New Method ◽  
Ammoniacal Nitrogen ◽  
Cent Solution ◽  
Base Exchange ◽  
Exchangeable Bases ◽  
Cent Sodium ◽  
Leaching Solution ◽  
Ammonium Compounds

A method for the determination of ammoniacal nitrogen in soils is described. It is an extension of the Hissink method for exchangeable bases to ammonium present in the soil. The working details are similar to the Hissink method, except that the leaching process is entirely carried out in the cold. The ammonia is distilled off with magnesium oxide.Using normal sodium chloride as a leaching solution and collecting half a litre of leachings for distillation with magnesia, results were obtained which showed excellent agreement with those by the aeration method. Similar results were obtained using 250 c.c. of 15 per cent, sodium chloride solution, but the results are on an average about 1·6 per cent, lower. With high proportions of ammoniacal nitrogen a second half litre of normal sodium chloride leachings should be taken, or half a litre of 15 per cent, solution used.The leaching method is economical of apparatus and water supply. It is therefore suitable for small laboratories with limited resources. It is fairly rapid: six estimations can be completed in a day.The close agreement of the new method with the aeration method suggests that the amount of ammoniacal nitrogen in the soil at any given time is not an arbitrary quantity depending on conditions of estimation, but a definite amount. It is improbable that any ammonium compounds exist in the soil apart from those which take part in base exchange.

An investigation of the method of Page and Williams for the determination of the saturation capacity of soils

1928 ◽  
Vol 18 (2) ◽  
pp. 257-265 ◽  
Author(s):  
P. E. Turner
Keyword(s):  
Calcium Carbonate ◽  
Calcium Ions ◽  
Exchange Reactions ◽  
Short Account ◽  
Exchangeable Bases ◽  
Reaction Proceeds ◽  
Leaching Solution ◽  
Saturation Capacity ◽  
The Difference

1. The value of the knowledge of the saturation capacity of a soil as an aid in its characterisation and classification is briefly stated.2. A short account is given of the more important methods in use for determination of saturation capacity.3. The theory underlying the method of Page and Williams, and the possible defects of the method are discussed.4. The results of an investigation of this method lead to the following conclusions:(a) Leaching the mixture of soil and calcium carbonate to 2 litres is in sufficient to displace from the soil all its exchangeable bases.(b) In view of this, it is recommended that 3 litres or more of filtrate be obtained, or preferably, the amount of soil employed be reduced to 10 grm.(c) The leaching solution remains in contact with the soil mixture for a period adequate for the normal sodium chloride solution to be saturated with calcium carbonate.(d) The difference in the amount of calcium, derived by solution from the carbonate, in the first and second litres of filtrate, is sufficiently small to be neglected.(e) The tardiness with which the reaction proceeds to completion is probably due to the difficulty experienced in displacing the final amounts of adsorbed ions, rather than to the presence of calcium ions in the leaching solution.(f) The incompleteness of the reaction renders the method of Hissink inaccurate for the calculation of the saturation capacity.(g) The variation in the character of the colloidal material of soils i s to some extent reflected in the value of the ratio of the calcium passing into solution through exchange reactions in the second litre, to that dissolved in this manner by the total volume of filtrate.

A new method for the determination of nitrates

1960 ◽  
Vol 23 ◽  
pp. 227-232 ◽  
Author(s):  
P WEST ◽  
G LYLES
Keyword(s):  
New Method

A New Method for the Determination of Plasma Activators of Fibrinolysis

1977 ◽  
Vol 37 (02) ◽  
pp. 210-215 ◽  
Author(s):  
R Margalit ◽  
E Gidron ◽  
Y Shalitin
Keyword(s):  
New Method ◽  
Effective Activator

SummaryThe term “effective activator” of plasminogen is proposed, to denote the resultant of activator-antiactivator interaction, and a method for the determination of the level of these activators is described. By adding axcess plasminogen to the euglobulin fraction of plasma the influence of the level of endogenous plasminogen and of the antiplasmin is eliminated. It is shown that the level of fibrinogen has very little bearing on the results. An effective activator unit is defined as equal to 1 CTA unit of urokinase activity on a fibrinogen-plasminogen substrate.

The Plasmin Inhibitors of Plasma

1964 ◽  
Vol 12 (01) ◽  
pp. 119-125 ◽  
Author(s):  
Y Shamash ◽  
A Rimon
Keyword(s):  
Human Plasma ◽  
New Method ◽  
Normal Amount ◽  
Caseinolytic Activity ◽  
Before And After ◽  
Plasmin Inhibitors

SummaryA new method for the assay of plasmin inhibitors in human plasma is described. The method consists of determination of the caseinolytic activity of a standard plasmin solution before and after incubation with the inhibitor, with lysine added to the mixture as a stabilizer of plasmin. Using this method, it was found that plasma contains enough inhibitors to inactivate 30 caseinolytic units of plasmin, or 10 times the normal amount of plasminogen in human plasma.

AGGLUTINATION INHIBITION REACTIONS FOR THE DETERMINATION OF GONADOTROPHINS

1969 ◽  
Vol 62 (1_Suppl) ◽  
pp. S95-S112 ◽  
Author(s):  
A. H. W. M. Schuurs
Keyword(s):  
Immune System ◽  
Quantitative Determination ◽  
Haemagglutination Inhibition ◽  
Latex Agglutination ◽  
Literature Survey ◽  
New Method ◽  
Test Fluid ◽  
Main Application ◽  
Test Systems

ABSTRACT Various techniques for sensitising erythrocytes and latex particles with gonadotrophins, particularly with HCG, are described. The haemagglutination inhibition reactions are generally interpreted by means of »erythrocyte settling patterns«. By a new method of evaluating these patterns a relatively precise quantitative determination is possible. Latex agglutination inhibition reactions on slides are particularly suitable as rapid qualitative tests. In cases where the maximum attainable sensitivity of the agglutination inhibition tests is insufficient, e. g. for determining LH concentrations in urine, the hormone in the test fluid has to be concentrated or extracted. An alternative method is a modified haemagglutination inhibition test for large volumes which is applicable to unconcentrated urine. Due to non-specific inhibitions the above-mentioned tests cannot be applied to unprocessed serum. Agglutination inhibition tests with HCG are already well advanced, pregnancy diagnosis being their main application. Now that highly purified HCG is available, a satisfactory specificity for these tests can be attained. If the immune system for HCG is used for estimating LH, it has to meet additional specificity requirements. Furthermore, the measure of cross-reaction and the choice of standard merit special attention. Finally, a literature survey is given of test systems in which LH and FSH were used as antigens.

Determination of quaternary ammonium compounds in food products by the method of ultra-performance liquid chromatography/high resolution mass-spectrometry

2020 ◽  
Vol 86 (8) ◽  
pp. 23-31
Author(s):  
V. G. Amelin ◽  
D. S. Bolshakov
Keyword(s):  
Mass Spectrometry ◽  
High Resolution ◽  
Quaternary Ammonium ◽  
High Resolution Mass Spectrometry ◽  
Food Products ◽  
Quaternary Ammonium Compounds ◽  
High Resolution Mass ◽  
Ammonium Compounds ◽  
Resolution Mass

The goal of the study is developing a methodology for determination of the residual amounts of quaternary ammonium compounds (QAC) in food products by UHPLC/high-resolution mass spectrometry after water-acetonitrile extraction of the determined components from the analyzed samples. The identification and determination of QAC was carried out on an «UltiMate 3000» ultra-high-performance liquid chromatograph (Thermo Scientific, USA) equipped with a «maXis 4G» high-resolution quadrupole-time-of-flight mass spectrometric detector and an ion spray «ionBooster» source (Bruker Daltonics, Germany). Samples of milk, cheese (upper cortical layer), dumplings, pork, chicken skin and ground beef were used as working samples. Optimal conditions are specified for chromatographic separation of the mixture of five QAC, two of them being a mixture of homologues with a linear structure (including isomeric forms). The identification of QAC is carried out by the retention time, exact mass of the ions, and coincidence of the mSigma isotopic distribution. The limits for QAC detection are 0.1 – 0.5 ng/ml, the determination limits are 1 ng/ml for aqueous standard solutions. The determinable content of QAC in food products ranges within 1 – 100 ng/g. The results of analysis revealed the residual amount of QAC present in all samples, which confirms data of numerous sources of information about active use of QAC-based disinfectants in the meat and dairy industry. The correctness of the obtained results is verified by introduction of the additives in food products at a level of 10 ng/g for each QAC. The relative standard deviation of the analysis results does not exceed 0.18. The duration of the analysis is 30 – 40 min.

Development of a New Method for Determination of the Oil Content from Microalgae Lipid Fraction

2017 ◽  
Vol 68 (4) ◽  
pp. 671-674
Author(s):  
Ana Maria Galan ◽  
Ioan Calinescu ◽  
Elena Radu ◽  
Elena Emilia Oprescu ◽  
Gabriel Vasilievici ◽  
...  
Keyword(s):  
Sunflower Oil ◽  
Oil Content ◽  
Lipid Fraction ◽  
New Method ◽  
Ms Analysis ◽  
Qualitative Determination ◽  
Tga Analysis

The purpose of this study was to develop a method for rapid quantitative and qualitative determination of the oil from microalgae lipid fraction obtained from Nannochloris sp biomass. The lipid fraction was first refluxed with 4% KOH in MeOH (60, 90, 120 min), followed by reaction with 20% BF3 in MeOH, using different times of reflux (90,120, 150 min) for each time of reflux with 4% KOH in MeOH. The FAME samples were analyzed by GC-MS analysis. 120 min reflux with 4% KOH in MeOH, 90 min with 20% BF3 in MeOH and a ratio lipid fraction: 4% KOH in MeOH: 20% BF3 in MeOH=1:20:27, were required to obtain the higher percent of oil in the microalgae lipid fraction. The relevance of the method developed was proved by TGA analysis and by transesterification of a sunflower oil sample in the same conditions.

METHOD FOR ESTIMATING ERRORS IN MEASURING INSTRUMENTS BY THE SPACE CATALOGUE ORBITS

2018 ◽  
pp. 76-84
Author(s):  
K. V. Sorokin ◽  
E. A. Sunarchina
Keyword(s):  
Dynamic Model ◽  
New Method ◽  
Measuring Instruments ◽  
Measuring Instrument ◽  
Software Complex

Improvement of orbits precision is one of the most important tasks of space surveillance catalogue maintenance. The solution of this problem is directly related to an adequate consideration of the errors of the coordinate information from the measuring instruments. The article consideresd a new method for estimating the precision of measuring instruments on the catalog orbits. To carry out such analysis, in PJSC «VIMPEL» special technological program was created. Main results of a study of radar errors with orbits of space surveillance catalogue was presented. Also, the results were compared with data of measuring instrument's calibration software complex. This software complex provides determination of satellite's position with errors less than 10 m. A new dynamic model of measuring instrument errors is proposed.

Sign in / Sign up

Export Citation Format

Share Document