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THERMOGRAVIMET
RIC ANALYSIS
PARTH VISHNUBHAI NAYI
MSC SEM 2 (APPLIED PHYSICS)
ROLL NO. : 19
INTRODUCTION
 Thermogravimetric analysis or thermal gravimetric analysis (TGA) is a method of
thermal analysis in which the mass of a sample is measured over time as the
temperature changes.
 Thermogravimetric analysis is method of thermal analysis in which changes in
physical and chemical properties of materials are measured as function of
increasing temperature rate or as a function of time.
PRINCIPLE
 In thermo-gravimetric analysis, the sample is heated in a given environment(air,
NO2, CO2,He,Ar,etc.) at controlled rate. The change in the weight of substance is
recorded as a function of temperature or time.
 The temperature is increased at a constant rate for a known initial weight of the
substance and the changes in weights are recorded as a function of temperature at
different time interval.
 This plot of weight change against temperature is called thermo-gravimetric curve
or thermo-gram, this is the basic principle of TGA.
TGA CURVE
 TG curves are normally plotted with the mass change in percentage on y-axis and
temperature (T) or time (t) on the x-axis.
 There are two temperatures in the reaction, Ti (procedural decomposition temp.) and
Tf (final temp.) representing the lowest temperature at which the onset of a mass
change is seen and the lowest temperature at which the process has been completed
respectively.
 The reaction temperature and interval (Tf-Ti) depend on the experimental condition;
they do not have any fixed value.
Instrumentation of TGA
Fig: Instrumentation / Block Diagram of TGA
Instrumentation of TGA:
 Recording balance
 Sample holder
 Furnace
 Temperature programmer / controller
( thermocouple)
 Recorder
Recording balance
 MICROBALANCE:
 A microbalance is used record a change in mass of sample/ substance.
An ideal microbalance must possess following features:
 It should provide electronic to record the change in mass using recorder.
 It should have the capacity of auto weight
 It operating should be user friendly.
 Morden microbalances have the ability to be not affected by vibrations
 Recorder balance :
After the sample has been placed on microbalance , it is left for 10-15 min to stabilizer.
Recorder balances are of to types:
A. Deflection-type instruments and
B. Null- types instruments
A. Deflection balances
a) Beam types
b) Helical type
c) Cantilevered beam
d) Torsion wire
B. Null point balances:
It consist of sensor which detects the deviation from the null point and
restores the balance to its null points by means of restoring force.
SAMPLE HOLDER
 The sample holder to be studied is placed in sampled holder or crucible. It is
attached to weighing arm of microbalance.
 There are different types of crucibles used such as
a) Shallow pans (used for volatile substances)
b) Deep crucibles ( Industrial scale calcination)
c) Loosely covered crucibles( self generated atm. Studies )
d) Retort cups ( Boiling point studies )
 They are made up from platinum , aluminum, quartz or alumina and some other
materials like graphite , stainless steel , glass etc.
FURNACE
 The furnace should be designed in such way that is produces a linear heating
range.
 It should have a hot zone which can hold sample and crucible and its temperature
corresponds to the temperature of furnace.
 there are different combinations of microbalance and furnace available. The furnace
heating coil should be wound in such a way that there is no magnetic interaction
between coil and sample or there can apparent mass change.
TEMPERATURE
PROGRAMMER/CONTROLLER :
 Temperature measurement is done in no. of ways thermocouple is the most
common technique.
 The position of temperature measuring device relative to the sample is very
important.
 The Major Types :
 The Thermocouple is placed near the sample container and it has no contact with
the sample container. This isn’t a good arrangement where low-pressure are
employed.
 The sample is kept inside the sample holder but not in contact with it. This
arrangement is better than that of 1ST because it responds to small temperature
changes.
 The thermocouple is placed either in contact with sample or with container . This is
the best arrangement of sample temperature detection.
Temperature programmer/controller :
Thermocouple in a thermo-balance:
RECORDER
 The output from the microbalance and furnace are recorded using either chart
recorder.
 The recording system are mainly of 2-types
1. Time-base potentiometric strip chart recorder.
2. X-Y recorder.
 In some instrument , light galvanometer, photographic paper recorders or one
recorder with two or more pens are also used.
 In the X-Y recorder, we get curves having plot of weight directly against
temperatures.
 However , the percentage mass change against temperature or time would be more
useful.
FACTORS AFFECTING TGA
1. Instrumental factors:
a) Furnace Heating rate: The temperature at which the compound (or sample)
decompose depends upon the heating rate. When the heating rate is high, the
decomposition temperature is also high. A heating rate of 3.5°C per minute is
usually recommended for reliable and reproducible TGA.
b) Furnace atmosphere: The atmosphere inside the furnace surrounding the sample
has profound effect on the decomposition temperature of the sample. A pure N2
gas from a cylinder passed through the furnace which provides an insert
atmosphere.
2. Sample characteristics:
a) Weight of sample: A small weight of sample is recommended using a small
weight eliminates the existence of temperature gradient throughout the sample.
b) Particle size of the sample : The particle size of the sample should be small and
uniform . The use of large particle or crystal may result in apparent, very rapid
weight loss during heating.
APPLICATIONS OF TGA
 TGA curve gives the information regarding chemical kinetics
 The atm. Of H2O present in the clay & soil can be determined.
 Solid state reactions.
 The determined of the composition of complex mixtures.
 TGA, we can determine the purity and thermal stability of both primary and
secondary standard.
 Thermal decomposition of organic , inorganic & polymerics compound’s can be
studied.
 Mechanics of polymer can be studied.
LIMITATIONS OF TGA
 TGA is applicable to solid compound’s only.
 As thermocouple is kept very close to sample but not in contact with the sample.
Therefore, exact temp. of the sample can not be detected.
TGA

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TGA

  • 1. THERMOGRAVIMET RIC ANALYSIS PARTH VISHNUBHAI NAYI MSC SEM 2 (APPLIED PHYSICS) ROLL NO. : 19
  • 2. INTRODUCTION  Thermogravimetric analysis or thermal gravimetric analysis (TGA) is a method of thermal analysis in which the mass of a sample is measured over time as the temperature changes.  Thermogravimetric analysis is method of thermal analysis in which changes in physical and chemical properties of materials are measured as function of increasing temperature rate or as a function of time.
  • 3. PRINCIPLE  In thermo-gravimetric analysis, the sample is heated in a given environment(air, NO2, CO2,He,Ar,etc.) at controlled rate. The change in the weight of substance is recorded as a function of temperature or time.  The temperature is increased at a constant rate for a known initial weight of the substance and the changes in weights are recorded as a function of temperature at different time interval.  This plot of weight change against temperature is called thermo-gravimetric curve or thermo-gram, this is the basic principle of TGA.
  • 4.
  • 5. TGA CURVE  TG curves are normally plotted with the mass change in percentage on y-axis and temperature (T) or time (t) on the x-axis.  There are two temperatures in the reaction, Ti (procedural decomposition temp.) and Tf (final temp.) representing the lowest temperature at which the onset of a mass change is seen and the lowest temperature at which the process has been completed respectively.  The reaction temperature and interval (Tf-Ti) depend on the experimental condition; they do not have any fixed value.
  • 6.
  • 7. Instrumentation of TGA Fig: Instrumentation / Block Diagram of TGA
  • 8. Instrumentation of TGA:  Recording balance  Sample holder  Furnace  Temperature programmer / controller ( thermocouple)  Recorder
  • 9. Recording balance  MICROBALANCE:  A microbalance is used record a change in mass of sample/ substance. An ideal microbalance must possess following features:  It should provide electronic to record the change in mass using recorder.  It should have the capacity of auto weight  It operating should be user friendly.  Morden microbalances have the ability to be not affected by vibrations
  • 10.  Recorder balance : After the sample has been placed on microbalance , it is left for 10-15 min to stabilizer. Recorder balances are of to types: A. Deflection-type instruments and B. Null- types instruments
  • 11. A. Deflection balances a) Beam types b) Helical type c) Cantilevered beam d) Torsion wire
  • 12. B. Null point balances: It consist of sensor which detects the deviation from the null point and restores the balance to its null points by means of restoring force.
  • 13. SAMPLE HOLDER  The sample holder to be studied is placed in sampled holder or crucible. It is attached to weighing arm of microbalance.  There are different types of crucibles used such as a) Shallow pans (used for volatile substances) b) Deep crucibles ( Industrial scale calcination) c) Loosely covered crucibles( self generated atm. Studies ) d) Retort cups ( Boiling point studies )  They are made up from platinum , aluminum, quartz or alumina and some other materials like graphite , stainless steel , glass etc.
  • 14.
  • 15. FURNACE  The furnace should be designed in such way that is produces a linear heating range.  It should have a hot zone which can hold sample and crucible and its temperature corresponds to the temperature of furnace.  there are different combinations of microbalance and furnace available. The furnace heating coil should be wound in such a way that there is no magnetic interaction between coil and sample or there can apparent mass change.
  • 16. TEMPERATURE PROGRAMMER/CONTROLLER :  Temperature measurement is done in no. of ways thermocouple is the most common technique.  The position of temperature measuring device relative to the sample is very important.
  • 17.  The Major Types :  The Thermocouple is placed near the sample container and it has no contact with the sample container. This isn’t a good arrangement where low-pressure are employed.  The sample is kept inside the sample holder but not in contact with it. This arrangement is better than that of 1ST because it responds to small temperature changes.  The thermocouple is placed either in contact with sample or with container . This is the best arrangement of sample temperature detection.
  • 19. RECORDER  The output from the microbalance and furnace are recorded using either chart recorder.  The recording system are mainly of 2-types 1. Time-base potentiometric strip chart recorder. 2. X-Y recorder.  In some instrument , light galvanometer, photographic paper recorders or one recorder with two or more pens are also used.  In the X-Y recorder, we get curves having plot of weight directly against temperatures.  However , the percentage mass change against temperature or time would be more useful.
  • 20. FACTORS AFFECTING TGA 1. Instrumental factors: a) Furnace Heating rate: The temperature at which the compound (or sample) decompose depends upon the heating rate. When the heating rate is high, the decomposition temperature is also high. A heating rate of 3.5°C per minute is usually recommended for reliable and reproducible TGA. b) Furnace atmosphere: The atmosphere inside the furnace surrounding the sample has profound effect on the decomposition temperature of the sample. A pure N2 gas from a cylinder passed through the furnace which provides an insert atmosphere.
  • 21. 2. Sample characteristics: a) Weight of sample: A small weight of sample is recommended using a small weight eliminates the existence of temperature gradient throughout the sample. b) Particle size of the sample : The particle size of the sample should be small and uniform . The use of large particle or crystal may result in apparent, very rapid weight loss during heating.
  • 22. APPLICATIONS OF TGA  TGA curve gives the information regarding chemical kinetics  The atm. Of H2O present in the clay & soil can be determined.  Solid state reactions.  The determined of the composition of complex mixtures.  TGA, we can determine the purity and thermal stability of both primary and secondary standard.  Thermal decomposition of organic , inorganic & polymerics compound’s can be studied.  Mechanics of polymer can be studied.
  • 23. LIMITATIONS OF TGA  TGA is applicable to solid compound’s only.  As thermocouple is kept very close to sample but not in contact with the sample. Therefore, exact temp. of the sample can not be detected.