Complexometric titration is a type of titration based on complex formation between the analyte and titrant. Complexometric titrations are useful for determining mixtures of metal ions in solution using an indicator with a marked color change to detect the endpoint. Complexometric titration can also be used to determine water hardness and is widely used in the medical industry due to its ability to work with microliter sample sizes. Common applications of complexometric titration include determining calcium content in cheese and phytic acid content. Acid-base and redox titrations are also important titration methods that have various applications in pharmaceuticals, biodiesel production, and determining vitamin C content in fruit juices among others.
Titration - principle, working and applicationSaloni Shroff
A brief introduction to the titration technique used to know the concentration of unknown solutions. different types, indicators used and its application in foods and nutrition is also described.
Titration - principle, working and applicationSaloni Shroff
A brief introduction to the titration technique used to know the concentration of unknown solutions. different types, indicators used and its application in foods and nutrition is also described.
THIS PRESENTATION IS FOR THE STUDENTS STUDYING IN SENIOR CLASSES .IT WILL HELP THE CHILD TO RECALL THE CONTENT IN SHORT TIME IT WILL HELP TO BUILD THE STRONG AND CLEAR CONCEPT KNOWLEDGE.
Titration is the slow addition of one solution of a known concentration (called a titrant) to a known volume of another solution of unknown concentration until the reaction reaches neutralization, which is often indicated by a color change.
THIS PRESENTATION IS FOR THE STUDENTS STUDYING IN SENIOR CLASSES .IT WILL HELP THE CHILD TO RECALL THE CONTENT IN SHORT TIME IT WILL HELP TO BUILD THE STRONG AND CLEAR CONCEPT KNOWLEDGE.
Titration is the slow addition of one solution of a known concentration (called a titrant) to a known volume of another solution of unknown concentration until the reaction reaches neutralization, which is often indicated by a color change.
Gram-positive spherical/ovoid cocci arranged in long chains; commonly in pairs
•Non-spore-forming, nonmotile
•Can form capsules and slime layers
•Facultative anaerobes,Capnophilic
•Catalase Negative
•Most parasitic forms are fastidious and require enriched media
•Small, non pigmented colonies
•Sensitive to drying, heat, and disinfectants
Analysis BOD is an important parameter in identifying the extend of pollution in a water body. This presentation explains the various methods of BOD analysis as per the APHA manual
intravenous fluid and electrolytes are important topics in medical science. potassium is one of the vital electrolytes of the human body. this presentation has a discussion on several iv fluids and potassium balance and also how to manage the potassium imbalance.
ANAMOLOUS SECONDARY GROWTH IN DICOT ROOTS.pptxRASHMI M G
Abnormal or anomalous secondary growth in plants. It defines secondary growth as an increase in plant girth due to vascular cambium or cork cambium. Anomalous secondary growth does not follow the normal pattern of a single vascular cambium producing xylem internally and phloem externally.
BREEDING METHODS FOR DISEASE RESISTANCE.pptxRASHMI M G
Plant breeding for disease resistance is a strategy to reduce crop losses caused by disease. Plants have an innate immune system that allows them to recognize pathogens and provide resistance. However, breeding for long-lasting resistance often involves combining multiple resistance genes
Phenomics assisted breeding in crop improvementIshaGoswami9
As the population is increasing and will reach about 9 billion upto 2050. Also due to climate change, it is difficult to meet the food requirement of such a large population. Facing the challenges presented by resource shortages, climate
change, and increasing global population, crop yield and quality need to be improved in a sustainable way over the coming decades. Genetic improvement by breeding is the best way to increase crop productivity. With the rapid progression of functional
genomics, an increasing number of crop genomes have been sequenced and dozens of genes influencing key agronomic traits have been identified. However, current genome sequence information has not been adequately exploited for understanding
the complex characteristics of multiple gene, owing to a lack of crop phenotypic data. Efficient, automatic, and accurate technologies and platforms that can capture phenotypic data that can
be linked to genomics information for crop improvement at all growth stages have become as important as genotyping. Thus,
high-throughput phenotyping has become the major bottleneck restricting crop breeding. Plant phenomics has been defined as the high-throughput, accurate acquisition and analysis of multi-dimensional phenotypes
during crop growing stages at the organism level, including the cell, tissue, organ, individual plant, plot, and field levels. With the rapid development of novel sensors, imaging technology,
and analysis methods, numerous infrastructure platforms have been developed for phenotyping.
ESR spectroscopy in liquid food and beverages.pptxPRIYANKA PATEL
With increasing population, people need to rely on packaged food stuffs. Packaging of food materials requires the preservation of food. There are various methods for the treatment of food to preserve them and irradiation treatment of food is one of them. It is the most common and the most harmless method for the food preservation as it does not alter the necessary micronutrients of food materials. Although irradiated food doesn’t cause any harm to the human health but still the quality assessment of food is required to provide consumers with necessary information about the food. ESR spectroscopy is the most sophisticated way to investigate the quality of the food and the free radicals induced during the processing of the food. ESR spin trapping technique is useful for the detection of highly unstable radicals in the food. The antioxidant capability of liquid food and beverages in mainly performed by spin trapping technique.
The use of Nauplii and metanauplii artemia in aquaculture (brine shrimp).pptxMAGOTI ERNEST
Although Artemia has been known to man for centuries, its use as a food for the culture of larval organisms apparently began only in the 1930s, when several investigators found that it made an excellent food for newly hatched fish larvae (Litvinenko et al., 2023). As aquaculture developed in the 1960s and ‘70s, the use of Artemia also became more widespread, due both to its convenience and to its nutritional value for larval organisms (Arenas-Pardo et al., 2024). The fact that Artemia dormant cysts can be stored for long periods in cans, and then used as an off-the-shelf food requiring only 24 h of incubation makes them the most convenient, least labor-intensive, live food available for aquaculture (Sorgeloos & Roubach, 2021). The nutritional value of Artemia, especially for marine organisms, is not constant, but varies both geographically and temporally. During the last decade, however, both the causes of Artemia nutritional variability and methods to improve poorquality Artemia have been identified (Loufi et al., 2024).
Brine shrimp (Artemia spp.) are used in marine aquaculture worldwide. Annually, more than 2,000 metric tons of dry cysts are used for cultivation of fish, crustacean, and shellfish larva. Brine shrimp are important to aquaculture because newly hatched brine shrimp nauplii (larvae) provide a food source for many fish fry (Mozanzadeh et al., 2021). Culture and harvesting of brine shrimp eggs represents another aspect of the aquaculture industry. Nauplii and metanauplii of Artemia, commonly known as brine shrimp, play a crucial role in aquaculture due to their nutritional value and suitability as live feed for many aquatic species, particularly in larval stages (Sorgeloos & Roubach, 2021).
Travis Hills' Endeavors in Minnesota: Fostering Environmental and Economic Pr...Travis Hills MN
Travis Hills of Minnesota developed a method to convert waste into high-value dry fertilizer, significantly enriching soil quality. By providing farmers with a valuable resource derived from waste, Travis Hills helps enhance farm profitability while promoting environmental stewardship. Travis Hills' sustainable practices lead to cost savings and increased revenue for farmers by improving resource efficiency and reducing waste.
Nucleophilic Addition of carbonyl compounds.pptxSSR02
Nucleophilic addition is the most important reaction of carbonyls. Not just aldehydes and ketones, but also carboxylic acid derivatives in general.
Carbonyls undergo addition reactions with a large range of nucleophiles.
Comparing the relative basicity of the nucleophile and the product is extremely helpful in determining how reversible the addition reaction is. Reactions with Grignards and hydrides are irreversible. Reactions with weak bases like halides and carboxylates generally don’t happen.
Electronic effects (inductive effects, electron donation) have a large impact on reactivity.
Large groups adjacent to the carbonyl will slow the rate of reaction.
Neutral nucleophiles can also add to carbonyls, although their additions are generally slower and more reversible. Acid catalysis is sometimes employed to increase the rate of addition.
Remote Sensing and Computational, Evolutionary, Supercomputing, and Intellige...University of Maribor
Slides from talk:
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Inter-Society Networking Panel GRSS/MTT-S/CIS Panel Session: Promoting Connection and Cooperation
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hematic appreciation test is a psychological assessment tool used to measure an individual's appreciation and understanding of specific themes or topics. This test helps to evaluate an individual's ability to connect different ideas and concepts within a given theme, as well as their overall comprehension and interpretation skills. The results of the test can provide valuable insights into an individual's cognitive abilities, creativity, and critical thinking skills
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Monitor common gases, weather parameters, particulates.
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What are greenhouse gasses how they affect the earth and its environment what is the future of the environment and earth how the weather and the climate effects.
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
3. C o m p l e x o m e t r i c t i t r a t i o n i s a t y p e o f t i t r a t i o n b a s e d
o n c o m p l e x f o r m a t i o n b e t w e e n t h e a n a l y t e a n d t i t r a n t
4. • Complexometric titrations are particularly for
determination of mixture of different metal ions
in solution. An indicator with a marked color
change is usually used to detect the end point of
titration.
• Complexometric titration is an efficient method
for determining the level of hardness of water.
Caused by accumulation of mineral ions.
• Complexometric is widely used in the medical
industry because of the microliter size sample
involved.
• The method is efficient in research related to
the biological cell.
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5. Complexometric Determination
of Calcium in Cheese
• 2 t o 3 g o f c h e e s e a r e a c h e d ,
d i s s o l v e d i n d i l u t e a c i d , a n d a d d e d
c a l c i u m c h l o r i d e i s b a c k t i t r a t e d
w i t h E D T A u s i n g h y d r o x y n a p h t h o l
b l u e a s i n d i c a t o r .
• S a m p l e s r e m a i n f r e e o f t u r b i d i t y ,
a n d t h e t i t r a t i o n e n d p o i n t i s
r e c o g n i z e d e a s i l y .
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I m p o r t a n c e
I n t e r e s t i n t h e c a l c i u m c o n t e n t o f
c h e e s e , h a s h e i g h t e n e d r e c e n t l y , n o t
o n l y d u e t o t h e n u t r i t i o n a l s i g n i f i c a n c e
o f c a l c i u m b u t a l s o t o i t s r e l a t i o n s h i p
w i t h c h e e s e q u a l i t y
6. P R O C E D U R E
c h e e s e s a m p l e s ( 2
t o 3 g ) w e r e
w e i g h e d w i t h a n
a n a l y t i c a l b a l a n c e .
Samples were dried overnight
at 100°C and ashed at 600°C.
After cooling, the ash was
wetted with 1 to 2 ml distilled
water followed by .5 ml
concentrated sulfuric acid.
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7. P R O C E D U R E
A small amount of additional distilled water
was added, if necessary, to disperse the ash,
and the slurry was transferred quantitatively
to a 250-ml flask.
The crucible was rinsed repeatedly with
distilled water until volume in the flask was
about 50 ml. If the mixture remained turbid
the flask was shaken mechanically for several
minutes until a clear solution was obtained.
Sufficient EDTA, usually 15 to 20 ml
measured from a burette, was added to the
flask to titrate approximately all calcium in
the sample.
The solution was stirred
magnetically and 8 ml sodium
hydroxide followed by about
100 mg indicator were added,
yielding a blue solution if all
calcium was titrated or red-
purple solution if titration
was incomplete.
In the latter
case, additional
EDTA was added
until color was
blue. Calcium
content was
calculated by
calculations.
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8. D e t e r m i n a t i o n o f P h y t i c
A c i d b y C o m p l e x o m e t r i c
T i t r a t i o n o f E x c e s s o f
I r o n ( l l )
• Phytine, phytate and myo-inositol
hexaphosphate are synonymous terms
for an organic phosphate, defined by
most workers as the calcium -
magnesium salt of myo-
inositolhexaphosphoric acid or phytic
acid.
Importance
• Phytic acid (I) and its sodium salts
occur in plant seeds and organic
soils, in which they constitute an
important phosphorus reserve. They
abound in cereals with a centripetal
location so its determination is
important.
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9. R e a g e n t s
• P h y t i c a c i d s t o c k s o l u t i o n ,
0 . 0 1 0 M .
• H y d r o c h l o r i c a c i d , 0 . 4 M a n d
2 % .
• I r o n ( I I ) s o l u t i o n i n 0 . 6 %
• S u l p h o s a l i c y l i c a c i d s o l u t i o n ,
2 0 % . i n d i c a t o r
• G l y c i n e .
• E D T A d i s o d i u m s a l t s o l u t i o n ,
0 . 0 1 M .
• S o d i u m s a l i c y l a t e s o l u t i o n , 1 0 % .
• S o d i u m s u l p h a t e s o l u t i o n , 5 % .
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10. P R O C E D U R E
Place 20.0 ml of phytic acid solution, containing
20.0ml hydrochloric acid, 20.0 ml iron(II) solution
and 20.0 ml sulphosalicylic acid solution in a 100-ml
test-tube.
Shake gently and seal the tube with a rubber cork
through which passes a narrow 30-cm long glass
tube, to prevent evaporation.
Place the tube in a boiling water-bath for 15 min,
then allow it to cool or cool it with tap water.
If a white precipitate forms, make sure that it has all
settled; in many instances naturally occurring samples
contain no phytic acid.
Taking care not to shake the tube, pipette exactly
20.0 ml from the supernatant liquid into a flask and
add distilled water to about 200ml. Heat to about 70
“C and, titrate with 0.010 M EDTA solution until the
intense red - maroon colour changes to clear yellow.
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11. An acid-base titration is
an experimental procedure
used to determined the
unknown concentration of
an acid or base by
precisely neutralizing it
with an acid or base of
known concentration.
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12. A P P L I C AT I O N S
Acid-base
titrations, i.e. the
neutralization
reaction between
acids and bases,
are very
frequently
performed in the
pharmaceutical
industry
acid-base
titrations are
often used for
Purity analysis
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15. Acid-base titration of Ibuprofen in
tablets
• Ibuprofen is an organic compound (its chemical name
is (RS)-2-[4-(2-methylpropyl)phenyl]propionic acid)
widely used as nonsteroidal anti-inflammatory drug
applied in fever, arthritis, and as pain reliever.
• Numerous drugs contain this compound, the most
popular are Ibum, Ibufen, Ibumax, Ibuprofen,
Ibuprom, MIG, Nurofen, Modafen etc.
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16. P R O C E D U R E
•Pour ca. 50 mL of glycerol and ca. 50
mL of hot water to flask and heat it to
ca. 60⁰C (the liquid is hot but does not
burn).
•Add 2-3 drops of Phenolphthalein and
add slowly, drop by drop, your titrant
NaOH solution, stirring the content
vigorously until rose color appears. Add
titrant solution to the burette up to
initial mark or note the actual level of
it.
•Place the tablet in the flask, crush it
with your glass stirring rod. Add
additional 1-2 drops of indicator and
titrate the content until red color
appears.
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17. Determination of CaCO3 in toothpaste
Acid base Titration
• Toothpaste is a daily-life
product, which is used
essentially to clean our
teeth
• Its major ingredients are
silica, calcium carbonate
and fluorine
• One of the most essential
substances is Calcium
Carbonate
7/8/2020
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18. B a c k T i t r a t i o n M e t h o d
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19. P R O C E D U R E
Taking sample Mixing HCl and toothpaste Adding indicatorHeating solution on hot pane
Titrate with 0.10 M NaOH until the color of the solution starting to change reaching the end point, check final pH and volume
of NaOH left in burette.
Checking initial pH
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20. R E D O X T I T R A T I O N
• A redox titration is based on a redox reaction between the analyte
and titrant.
• It may involve the use of a redox indicator and/or a
potentiometer.
• Oxidation-reduction titrations (redox) are used for checking the
purity of raw materials, fillers and preservatives.
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21. D e t e r m i n a t i o n o f A s c o r b i c
A c i d i n C o m m e r c i a l F r u i t
J u i c e s b y R e d o x T i t r a t i o n
• A number of commercial juices
of different brands are
available in the markets.
These juices are consumed
daily by all classes of
population all over the world.
• Ascorbic acid (AA) contents is
determined by a procedure
based on iodometric titration
where dark blue complex
forms in the presence of
starch at the end point
Ascorbic acid (AA)
also known as
vitamin C can be
obtained from fruits
or vegetables and
multi-vitamin
supplements
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22. I O D O M E T R I C
T I T R A T I O N
• In this method, iodine reacts
with ascorbic acid to produce
dehydroascorbic acid which is
a colorless product.
• Iodine also reacts with starch
to produce a dark blue
product
• In presence of both ascorbic
acid and starch, the iodine
preferably reacts with the
Vitamin C instead of the
starch. Therefore, when
iodine is added in the
presence of both substances,
the ascorbic acid reacts and
the products are colorless.
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23. P R O C E D U R E
• Preparing iodine solution
• Preparing starch indicator solution
• Preparing of drink sample
• Standardization of the iodine solution
with the Ascorbic Acid standard
solution
Titration
• Aliquot of the sample solution
prepared above transferred into a
conical flask, 2 ml of oxalic acid,
about 150 mL of distilled water and 1
mL of starch indicator solution.
• Samples were titrated with 0.005 molL
−1 iodine solution. The endpoint of
the titration was identified as the first
distinct trace of a dark blue-black
color due to the formation of starch-
iodine complex.
Iodine solution changes rapidly because
Iodine is a halogen gas that evaporates
quickly. Therefore, iodine solutions need
to be standardized all the time during the
experimental procedure. Ascorbic acid is
also susceptible to oxidation by
atmospheric oxygen over time. For this
reason, the sample was prepared
immediately before the titrations. In
addition to this, a small amount of oxalic
acid (2 mL) was added to standard
ascorbic acid solution in order to
minimize the probability of oxidation of
ascorbic acid.
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24. S o d i u m S u l f a t e o f C o s m e t i c s ( R e d o x
t i t r a t i o n B Y A u t o m a t i c P o t e n t i o m e t r i c
T i t r a t o r )
Importance
Sodium sulfate is a
substance being
harmless to human
contained in hot
spring and believed to
smooth the skin. It is
used as auxiliary agent
in powder shampoo. It
helps to absorb dirt
and stains with
surface active agent.
Lead sulfate
precipitates are
formed when Sodium
sulfate contained in
cosmetics is titrated
with lead ion solution
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25. Redox titration By Automatic
Potentiometric Titrator
With Potassium ferricyan
-ferrocyanide indicator
is added, as Sulfate ion
decreases, Fe(II)ion
changes to Fe(III)ion also
changing electrode
potential.
Depending on composition,
some cosmetics may not
show a sharp inflexion,
however, EP can be
determined by setting an
appropriate rate of change
(RC) for detection.
At the endpoint of sulfate ion
precipitation, only Fe (III) ion
remains with a sharp potential
inflexion, which is detected by the
platinum electrode, and thus
concentration of Sodium sulfate is
obtained from titration volume.
• Reagent
Titrant : Lead nitrate
Solvent : Ethanol
Indicator: Potassium
Ferricyan-ferrocyanide
Hydrochloric acid
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26. P R O C E D U R E
Preparation of sample in
a beaker, and adding of
HCl and Ethanol.
Adding Potassium ferricyan
-ferrocyanide test
solution.
Titration with Lead nitrate
up to the endpoint to
obtain Sodium sulfate.
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27. The Determination of
Hypochlorite in Bleach
An aqueous solution
of sodium
hypochlorite (NaOCl)
is a clear, slightly
yellow liquid, and is
commonly known as
bleach.
Aside from its
uses as a
bleaching agent,
sodium
hypochlorite
solutions are also
used as sterilizing
agents and in
water treatment.
Industrial uses
include agriculture,
food, paper
production, and
textiles. Sodium
hypochlorite is also
added to waste
water to reduce
odors.
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28. P R O C E D U R E
sodium hypochlorite,
hydrochloric acid,
iodide ion, and
starch are combined
to form a starch–
triiodide blue
complex that has a
concentration that is
proportional to the
amount of sodium
hypochlorite in the
solution.
the starch-
triiodide product
is titrated by
sodium
thiosulfate to
form a colorless
solution of
iodide,
dithionate, and
uncomplexed
starch
The hypochlorite acts as
a limiting reagent,
determining how much
triiodide is produced. We
can then titrate the
triiodide-starch complex
with the thiosulfate to
determine the
concentration of the
complex formed. This
can then be used to
calculate the initial
concentration of
hypochlorite.
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29. 7/8/2020
29REFERENCES
Ismail, M., Ali, S., & Hussain, M. (2014). Quantitative determination of ascorbic acid in commercial fruit juices by redox
titration. Int. J. Pharm. Qual. Assur., 5, 22-25.
Kindstedt, P. S., & Kosikowski, F. V. (1985). Improved complexometric determination of calcium in cheese. Journal of
Dairy Science, 68(4), 806-809.ChemBuddy. (2009). Back Titration [Online]. Available:
http://www.titrations.info/backtitration
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Muang, Chonburi 20000, Lot no. 10-1-5513295
R. Garcia-Villanova, R. J. Garcia-Villanova and C. Ruiz de Lope Department of Chemical Analysis, Food Science and
Toxicology, Faculty of Pharmacy, University of Granada, Granada, Spain
Shui-Ping Yang* and Ruei-Ying Tsai Department of Chemistry, National Changhua University of Education, Changhua
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