In this presentation I have mentioned whatever the possible relevant content is required for this method
Citation Is done at the end of slide.
Content is up to date & true to my belief.
Thanks & Best Regards.
Anurag Pandey
B.Pharm (FACULTY OF PHARMACY, INVERTIS UNIVERSITY)
M.Pharm (INSTITUTE OF PHARMACY, NIRMA UNIVERSITY)
Email :- anurag.dmk05@gmail.com
Total Nitrogen Determination - Traditional and Modern MethodsKasun Prabhashwara
This slideshow contains a short overview of importance of total nitrogen determination, traditional Kjeldahl method, its improvements and Dumas method of total nitrogen determination.
In this presentation I have mentioned whatever the possible relevant content is required for this method
Citation Is done at the end of slide.
Content is up to date & true to my belief.
Thanks & Best Regards.
Anurag Pandey
B.Pharm (FACULTY OF PHARMACY, INVERTIS UNIVERSITY)
M.Pharm (INSTITUTE OF PHARMACY, NIRMA UNIVERSITY)
Email :- anurag.dmk05@gmail.com
Total Nitrogen Determination - Traditional and Modern MethodsKasun Prabhashwara
This slideshow contains a short overview of importance of total nitrogen determination, traditional Kjeldahl method, its improvements and Dumas method of total nitrogen determination.
In this slide contains Determination of Acid value, Saponification value and Ester value.
Presented by: P.NARESH (Department of pharmaceutical analysis).RIPER, anantapur
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Presented by: K. SANDHYA RANI (Department of pharmaceutical analysis).RIPER, anantapur
In this slide contains Determination of Acid value, Saponification value and Ester value.
Presented by: P.NARESH (Department of pharmaceutical analysis).RIPER, anantapur
In this slide contains definition and determination of Iodine value, Rancidity, Peroxide value.
Presented by: K. SANDHYA RANI (Department of pharmaceutical analysis).RIPER, anantapur
Preparation, reactions, Acidity, effect of substituents on acidity, structure and uses of carboxylic acid and identification tests for carboxylic acid, amide and ester
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In this book, we use conservation of energy techniques on a fluid element to derive the Modified Bernoulli equation of flow with viscous or friction effects. We derive the general equation of flow/ velocity and then from this we derive the Pouiselle flow equation, the transition flow equation and the turbulent flow equation. In the situations where there are no viscous effects , the equation reduces to the Bernoulli equation. From experimental results, we are able to include other terms in the Bernoulli equation. We also look at cases where pressure gradients exist. We use the Modified Bernoulli equation to derive equations of flow rate for pipes of different cross sectional areas connected together. We also extend our techniques of energy conservation to a sphere falling in a viscous medium under the effect of gravity. We demonstrate Stokes equation of terminal velocity and turbulent flow equation. We look at a way of calculating the time taken for a body to fall in a viscous medium. We also look at the general equation of terminal velocity.
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Inspired by David Donoho's vision, this talk aims to revisit the three crucial pillars of frictionless reproducibility (data sharing, code sharing, and competitive challenges) with the perspective of deep software variability.
Our observation is that multiple layers — hardware, operating systems, third-party libraries, software versions, input data, compile-time options, and parameters — are subject to variability that exacerbates frictions but is also essential for achieving robust, generalizable results and fostering innovation. I will first review the literature, providing evidence of how the complex variability interactions across these layers affect qualitative and quantitative software properties, thereby complicating the reproduction and replication of scientific studies in various fields.
I will then present some software engineering and AI techniques that can support the strategic exploration of variability spaces. These include the use of abstractions and models (e.g., feature models), sampling strategies (e.g., uniform, random), cost-effective measurements (e.g., incremental build of software configurations), and dimensionality reduction methods (e.g., transfer learning, feature selection, software debloating).
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Exposé invité Journées Nationales du GDR GPL 2024
2. HISTORY OF KJELDAHL METHOD
IN THE YEAR OF 1883, MARCH 7TH JOHAN GUSTAV
CHRISTOFFER THORSAGER KJELDAHL , A DANISH CHEMIST
DEVELOPED THIS METHOD.
OBJECTIVE
“ QUALITATIVE DETERMINATION OF ORGANIC AS WELL
AS INORGANIC NITROGEN (N2) IN THE SUBSTANCES .”
PG 2
5. THE PROCEDURE INVOLVES THREE MAJOR STEPS
DIGESTION: For decomposition of nitrogen sample utilizing a concentrated acid
solution(H2SO4) a catalyst(CuSO4) and K2SO4 for boiling point increasing agent. As
a result Ammonium Sulphate produce.
Nitrogenous Compound + H2SO4 +CuSO4 + K2SO4 =
(NH4)2SO4 + H2O + CO2 + Other by-products
DISTILLATION: Adding excess base to the acid digestion mixture to convert NH4+
to NH3, followed by boiling and condensation of the NH3 gas in a receiving solution.
(NH4)2SO4 + 2NaOH = 2NH3 ↑ + Na2SO4 + 2H2O
TITRATION: To quantify the amount of ammonia in the receiving solution.
pg 5
6. TITRATION
Reaction with Boric Acid (H3BO3): [Direct titration]
If Boric Acid is receiving solution then the Ammonia produce in
distillation is react with H3BO3 and produce AMMONIUM BORATE
(NH4+H2BO3-), it can directly titrated against standard acid by using
METHYL RED as an indicator.
NH3 + H3BO3 = NH4+H2BO3-
ADVANTAGES:
1) Prevent loss of ammonia by volatilization,
2) No need to back titration, too weak acid to interfere further titration. Pg 6
7. TITRATION
Reaction with Hydrochloric Acid (HCl): [Back titration]
The ammonia is captured by a, carefully measured excess of a
standardized acid solution in the receiving flask. The excess of acid
in the receiving solution keeps the pH low, and the indicator does not
change color.
NH3 + HCl (in excess) = NH4+Cl- + HCl (left back)
The excess acid solution is exactly neutralized by a carefully
measured standardized alkaline base solution such as sodium hydroxide. A
color change is produced at the end point of the titration.
HCl + NaOH = NaCl + H2O
V ml of X (N) NaOH = V ml of X (N) HCl = V ml of X (N) NH3
pg 7
8. AdvantagesANDDisadvantages
ADVANTAGES
• It is a standard method of determining nitrogen content on protein in food sample.
• It can measured the total nitrogen in soil sample.
DISADVANTAGES
• It does not give a measure of the true protein, since all nitrogen in food is not in the form of protein.
• Different proteins need different correction factors because they have different amino acid sequence .
• The use of concentrated sulphuric acid at high temperatures make some kind of hazards, as does the use of
some of the possible catalyst.
• Kjeldahl method is not applicable to compounds containing nitrogen in nitro and azo
groups and nitrogen present in rings (e.g. pyridine , quinoline, isoquinoline) as nitrogen of these compounds
does not convert to ammonium sulfate under the conditions of this method.
• This is a time consuming method.
Editor's Notes
This is the question that your experiment answers
List all of the steps used in completing your experiment.
Remember to number your steps.
Establish hypothesis before you begin the experiment. This should be your best educated guess based on your research.