SlideShare a Scribd company logo
5
Most read
10
Most read
14
Most read
The Solids State
General properties
Crystalline Solids
Amorphous Solids
Melting point
General properties
Solids are much denser than both gases and liquids due to
the presence of very strong intermolecular forces.
Solids are essentially incompressible (small empty spaces)
Solids have definite volume and shape (rigid, not fluid)
Solids have no
translational
motion (only
vibration)
Crystalline Solids
Crystalline solids, such as sodium chloride, and menthol,
are composed of structural units arranged in fixed
geometric patterns or lattices.
Menthol
Sodium Chloride
Crystalline Solids
Crystalline solids show definite melting points, passing
rather sharply from the solid to the liquid state.
The morphology of a crystalline form is often referred to as
its habit, where the crystal habit is defined as having the
same structure but different outward appearance.
Crystalline Solids
Types of crystalline solids
The units that constitute the crystal structure can be atoms,
molecules, or ions
.
Ionic Solid
Lattice units consist of
ions held together by
ionic bonds e.g. NaCl
Atomic Solid
Lattice units consist of
atoms held together by
covalent bonds e.g.
diamond
Molecular Solid
Lattice units consists of
molecules held together
by van der Waals forces
e.g. Solid CO2
Ionic and atomic crystals in general are hard and brittle and have high melting
points, while molecular crystals are soft and have relatively low melting points.
Crystalline Solids
Types of crystalline solids
Metallic crystals are composed of positively charged ions
in a field of freely moving electrons. The atoms are held
together by metallic bonding.
Metals are good conductors
of electricity because of
the free movement of the
electrons in the lattice.
Metals may be soft or hard
and have low or high
melting points.
Amorphous Solids
Amorphous solids may be considered as supercooled
liquids in which the molecules are arranged in a
somewhat random manner as in the liquid state.
Amorphous Crystalline
They differ from crystalline solids in that they tend to flow
when subjected to sufficient pressure over a period of
time, and they do not have definite melting points.
Amorphous Solids
The amorphous state is unstable compared to the
crystalline solid (it has higher energy than crystalline
solid).
The pharmaceutical advantages of amorphous solid is its
higher solubility and bioavailability.
Its pharmaceutical disadvantages is its low stability (over
time, amorphous solid may transform to the more stable
crystalline state).
Melting point
Heat of fusion
The temperature at which a solid passes into liquid state is
known as the melting point. It is also the freezing point
of the liquid state of that solid.
The melting point of a pure crystalline solid (or freezing
point of a liquid) is the temperature at which the pure
liquid and solid exist in equilibrium.
Normal melting or freezing point is the temperature of the
equilibrium mixture at an external pressure of 1 atm.
Unlike the boiling point, the melting point is relatively
insensitive to pressure because the solid/liquid transition
represents only a small change in volume.
Melting point
Heat of fusion
The heat (energy) absorbed when 1 g of a solid melts or the
heat liberated when it freezes is known as the latent heat
of fusion.
∆𝑻 𝑽𝒍 − 𝑽 𝒔
= 𝑻
∆𝑷 ∆𝑯 𝒇
Vl and Vs: the molar volumes (cm3/mole) of the liquid and solid,
respectively (Molar volume is computed by dividing the gram
molecular weight by the density of the compound).
ΔHf : the molar heat of fusion (the amount of heat absorbed when 1
mole of the solid changes into liquid)
ΔT: the change of melting point brought about by a pressure change
of ΔP.
Melting point
Intermolecular forces
• The heat of fusion may be considered as the heat
required to increase the interatomic or intermolecular
distances in crystals, thus allowing melting (increased
molecular motion) to occur.
• A crystal that is bound together by weak forces
generally has a low heat of fusion and a low melting
point, whereas one bound together by strong forces has
a high heat of fusion and a high melting point.
Thermal analysis
Applications
Thermal analysis has many applications in pharmaceutical
industry and quality control such as:
Melting points for organic and inorganic compounds are
often used for thermal analysis for-
Characterization and identification of compounds.
Determination of purity, polymorphism, and stability.
Investigation of drug compatibility with excipient(s).
Thermal analysis
Definition
Thermal analysis is a number of methods for observing
physical and chemical changes (e.g melting point) of a
material upon heating or cooling.
The most common types of thermal analysis are:
Differntail scanning calorimetry (DSC)
Differential thermal analysis (DTA),
Thermogravimetric analysis (TGA)
Thermomechanical analysis (TMA).
Polymorphism
• Some elements like carbon (Dimond, graphite) and
sulphur exist in more than one crystalline form which is
known as polymorphism
• Diamond is metastable (less stable) form of carbon
• Polymorphs exhibit different-
• Melting points
• Solubility
• Formation of different polymorphs depend upon
crystallization conditions (Level of supersaturation,
temperature)
Pharmaceutical significance of
polymorphs
• Nearly all long chain organic compounds exhibit polymorphism
• Eg: Triglyceride tristearin shows
• Low melting point metastable (α)
• Beta prime (β’)
• High melting point Stable beta (β)
• Theobroma (coca butter) shows 4 forms γ, α, β’ and β. For
making suppositories Theobroma should be melted at lowest
possible temperature (33C) so that stable polymorph (β MP
34.5C)) should not destroy.
• Because of difference in solubilities of polymorphs, one may be
more active therapeutically than other. E.g. Sulfameter
antimicrobial form II is more active than Form III.
• Cortisone acetate suspension … out of 5 forms only one is stable
in presence of water. During preparation of suspension stable form
should be available to avoid caking.
References
Sinko, P. J. Martin's physical pharmacy and pharmaceutical sciences:
physical chemical and biopharmaceutical principles in the
pharmaceutical sciences, Philadelphia, Lippincott Williams &
Wilkins.

More Related Content

PDF
PDF
States of matter and properties of matter
PPTX
State of matter and properties of matter (Part-7)(Solid-crystalline, Amorpho...
PPTX
Clinical trials its types and designs
PPT
Crystal Growth_Introduction
PPT
Chemical properties
PPT
Solid state chemistry
States of matter and properties of matter
State of matter and properties of matter (Part-7)(Solid-crystalline, Amorpho...
Clinical trials its types and designs
Crystal Growth_Introduction
Chemical properties
Solid state chemistry

What's hot (20)

DOCX
Amorphous and crystalline solids by www.topcoaching.com
PPTX
Solubility of drugs
PPT
Solubilization
PPTX
Solid-Crystalline, Amorphous & Polymorphism
PPT
Solubility
PPT
Polymers and their properties
PPTX
Materials of pharmaceutical plant construction- Pharmaceutical Engineering
PPTX
Micelle and Critical Micelle Concentration
PPTX
Properties of polymers
PPTX
Polymers
PPTX
Fractional Distillation
PPTX
AMORPHOUS and CRYSTALLINE SOLIDS.pptx
PPTX
Polymorphism and crystallisation : The mysterious phenomenon
PPTX
Recrystallization
PDF
Pharmaceutical Engineering: Size reduction
PPTX
UNIT OPERATIONS : PHARMACEUTICAL ENGINEERING ON BASICS AND APPLICATION
PDF
Pharmaceutical Engineering: Crystallization
PPTX
State of matter and properties of matter (Part-6)(Relative humidity, Liquid ...
Amorphous and crystalline solids by www.topcoaching.com
Solubility of drugs
Solubilization
Solid-Crystalline, Amorphous & Polymorphism
Solubility
Polymers and their properties
Materials of pharmaceutical plant construction- Pharmaceutical Engineering
Micelle and Critical Micelle Concentration
Properties of polymers
Polymers
Fractional Distillation
AMORPHOUS and CRYSTALLINE SOLIDS.pptx
Polymorphism and crystallisation : The mysterious phenomenon
Recrystallization
Pharmaceutical Engineering: Size reduction
UNIT OPERATIONS : PHARMACEUTICAL ENGINEERING ON BASICS AND APPLICATION
Pharmaceutical Engineering: Crystallization
State of matter and properties of matter (Part-6)(Relative humidity, Liquid ...
Ad

Similar to Solid state (20)

PDF
1-2-PhysicalState of Matter.pdf
PPTX
State of matter (Physical Pharmacy)
PPTX
PPT_PDF_pp _UNIT_2baa_somapoMATTER .pptx
PPTX
States of matter
PPTX
Pp unit 2
PPTX
Unit 3 PPT.pptx
PPT
Heat treatmet of metal alloys
PPT
Ch 1 Matter in Our Surroundings Slide show 3.ppt
PPT
2. PPT DOWNLOADED.ppt
PPTX
Chapter 2 chemical engineering.pptxvihihigigicugu
PPTX
States of Matter Unit-2 (Physical Pharmaceutics-1)
PPT
States and Changes (Matter)
PPTX
Matter & its composition
PPT
states_of_matter.ppt
PPT
Ppp8 Glassy State And Glass Transition Temperature
PPTX
General Chemistry.pptx
PPT
Preformulation -1.- Industrial Pharmacyppt
PPTX
States of matter.pptx
PPTX
Unit-III Phase diagram & Iron Carbon Diagram.pptx
PPTX
STATES OF MATTER
1-2-PhysicalState of Matter.pdf
State of matter (Physical Pharmacy)
PPT_PDF_pp _UNIT_2baa_somapoMATTER .pptx
States of matter
Pp unit 2
Unit 3 PPT.pptx
Heat treatmet of metal alloys
Ch 1 Matter in Our Surroundings Slide show 3.ppt
2. PPT DOWNLOADED.ppt
Chapter 2 chemical engineering.pptxvihihigigicugu
States of Matter Unit-2 (Physical Pharmaceutics-1)
States and Changes (Matter)
Matter & its composition
states_of_matter.ppt
Ppp8 Glassy State And Glass Transition Temperature
General Chemistry.pptx
Preformulation -1.- Industrial Pharmacyppt
States of matter.pptx
Unit-III Phase diagram & Iron Carbon Diagram.pptx
STATES OF MATTER
Ad

More from Mirza Salman Baig (20)

PDF
Suspension sb pci
PDF
F.y.b. pharm syllbus
PDF
Interfacial Phenomenon SB
PDF
Buffer: Applications and capacity SB
PDF
Sorensen's pH scale SB
PDF
Cosmetics SB 2020
PDF
Suppositories SB 2020
PDF
Semisolids sb 2020
PDF
States of Matter SB
PDF
Biphasic systems suspension sb
PDF
Large scale manufacture of suspension emulsion sb
PDF
Introduction biphasic system suspension emulsion
PDF
Solubility of drugs
PDF
Dissolution v2
PDF
Diffusion v2
PDF
Accelerated stability testing v2
PDF
Chemical kinetics v2
PDF
Buffer and Buffer capacity
PDF
Buffer and Buffer capacity
PDF
Interfacial Phenomena
Suspension sb pci
F.y.b. pharm syllbus
Interfacial Phenomenon SB
Buffer: Applications and capacity SB
Sorensen's pH scale SB
Cosmetics SB 2020
Suppositories SB 2020
Semisolids sb 2020
States of Matter SB
Biphasic systems suspension sb
Large scale manufacture of suspension emulsion sb
Introduction biphasic system suspension emulsion
Solubility of drugs
Dissolution v2
Diffusion v2
Accelerated stability testing v2
Chemical kinetics v2
Buffer and Buffer capacity
Buffer and Buffer capacity
Interfacial Phenomena

Recently uploaded (20)

PPTX
Institutional Correction lecture only . . .
PPTX
Pharmacology of Heart Failure /Pharmacotherapy of CHF
PDF
3rd Neelam Sanjeevareddy Memorial Lecture.pdf
PDF
Pre independence Education in Inndia.pdf
PDF
Abdominal Access Techniques with Prof. Dr. R K Mishra
PDF
Supply Chain Operations Speaking Notes -ICLT Program
PDF
O7-L3 Supply Chain Operations - ICLT Program
PDF
ANTIBIOTICS.pptx.pdf………………… xxxxxxxxxxxxx
PDF
Module 4: Burden of Disease Tutorial Slides S2 2025
PDF
Origin of periodic table-Mendeleev’s Periodic-Modern Periodic table
PDF
Business Ethics Teaching Materials for college
PDF
O5-L3 Freight Transport Ops (International) V1.pdf
PPTX
Cell Structure & Organelles in detailed.
PDF
Saundersa Comprehensive Review for the NCLEX-RN Examination.pdf
PDF
Mark Klimek Lecture Notes_240423 revision books _173037.pdf
PPTX
Final Presentation General Medicine 03-08-2024.pptx
PPTX
IMMUNITY IMMUNITY refers to protection against infection, and the immune syst...
PDF
STATICS OF THE RIGID BODIES Hibbelers.pdf
PDF
TR - Agricultural Crops Production NC III.pdf
PPTX
BOWEL ELIMINATION FACTORS AFFECTING AND TYPES
Institutional Correction lecture only . . .
Pharmacology of Heart Failure /Pharmacotherapy of CHF
3rd Neelam Sanjeevareddy Memorial Lecture.pdf
Pre independence Education in Inndia.pdf
Abdominal Access Techniques with Prof. Dr. R K Mishra
Supply Chain Operations Speaking Notes -ICLT Program
O7-L3 Supply Chain Operations - ICLT Program
ANTIBIOTICS.pptx.pdf………………… xxxxxxxxxxxxx
Module 4: Burden of Disease Tutorial Slides S2 2025
Origin of periodic table-Mendeleev’s Periodic-Modern Periodic table
Business Ethics Teaching Materials for college
O5-L3 Freight Transport Ops (International) V1.pdf
Cell Structure & Organelles in detailed.
Saundersa Comprehensive Review for the NCLEX-RN Examination.pdf
Mark Klimek Lecture Notes_240423 revision books _173037.pdf
Final Presentation General Medicine 03-08-2024.pptx
IMMUNITY IMMUNITY refers to protection against infection, and the immune syst...
STATICS OF THE RIGID BODIES Hibbelers.pdf
TR - Agricultural Crops Production NC III.pdf
BOWEL ELIMINATION FACTORS AFFECTING AND TYPES

Solid state

  • 1. The Solids State General properties Crystalline Solids Amorphous Solids Melting point
  • 2. General properties Solids are much denser than both gases and liquids due to the presence of very strong intermolecular forces. Solids are essentially incompressible (small empty spaces) Solids have definite volume and shape (rigid, not fluid) Solids have no translational motion (only vibration)
  • 3. Crystalline Solids Crystalline solids, such as sodium chloride, and menthol, are composed of structural units arranged in fixed geometric patterns or lattices. Menthol Sodium Chloride
  • 4. Crystalline Solids Crystalline solids show definite melting points, passing rather sharply from the solid to the liquid state. The morphology of a crystalline form is often referred to as its habit, where the crystal habit is defined as having the same structure but different outward appearance.
  • 5. Crystalline Solids Types of crystalline solids The units that constitute the crystal structure can be atoms, molecules, or ions . Ionic Solid Lattice units consist of ions held together by ionic bonds e.g. NaCl Atomic Solid Lattice units consist of atoms held together by covalent bonds e.g. diamond Molecular Solid Lattice units consists of molecules held together by van der Waals forces e.g. Solid CO2 Ionic and atomic crystals in general are hard and brittle and have high melting points, while molecular crystals are soft and have relatively low melting points.
  • 6. Crystalline Solids Types of crystalline solids Metallic crystals are composed of positively charged ions in a field of freely moving electrons. The atoms are held together by metallic bonding. Metals are good conductors of electricity because of the free movement of the electrons in the lattice. Metals may be soft or hard and have low or high melting points.
  • 7. Amorphous Solids Amorphous solids may be considered as supercooled liquids in which the molecules are arranged in a somewhat random manner as in the liquid state. Amorphous Crystalline They differ from crystalline solids in that they tend to flow when subjected to sufficient pressure over a period of time, and they do not have definite melting points.
  • 8. Amorphous Solids The amorphous state is unstable compared to the crystalline solid (it has higher energy than crystalline solid). The pharmaceutical advantages of amorphous solid is its higher solubility and bioavailability. Its pharmaceutical disadvantages is its low stability (over time, amorphous solid may transform to the more stable crystalline state).
  • 9. Melting point Heat of fusion The temperature at which a solid passes into liquid state is known as the melting point. It is also the freezing point of the liquid state of that solid. The melting point of a pure crystalline solid (or freezing point of a liquid) is the temperature at which the pure liquid and solid exist in equilibrium. Normal melting or freezing point is the temperature of the equilibrium mixture at an external pressure of 1 atm. Unlike the boiling point, the melting point is relatively insensitive to pressure because the solid/liquid transition represents only a small change in volume.
  • 10. Melting point Heat of fusion The heat (energy) absorbed when 1 g of a solid melts or the heat liberated when it freezes is known as the latent heat of fusion. ∆𝑻 𝑽𝒍 − 𝑽 𝒔 = 𝑻 ∆𝑷 ∆𝑯 𝒇 Vl and Vs: the molar volumes (cm3/mole) of the liquid and solid, respectively (Molar volume is computed by dividing the gram molecular weight by the density of the compound). ΔHf : the molar heat of fusion (the amount of heat absorbed when 1 mole of the solid changes into liquid) ΔT: the change of melting point brought about by a pressure change of ΔP.
  • 11. Melting point Intermolecular forces • The heat of fusion may be considered as the heat required to increase the interatomic or intermolecular distances in crystals, thus allowing melting (increased molecular motion) to occur. • A crystal that is bound together by weak forces generally has a low heat of fusion and a low melting point, whereas one bound together by strong forces has a high heat of fusion and a high melting point.
  • 12. Thermal analysis Applications Thermal analysis has many applications in pharmaceutical industry and quality control such as: Melting points for organic and inorganic compounds are often used for thermal analysis for- Characterization and identification of compounds. Determination of purity, polymorphism, and stability. Investigation of drug compatibility with excipient(s).
  • 13. Thermal analysis Definition Thermal analysis is a number of methods for observing physical and chemical changes (e.g melting point) of a material upon heating or cooling. The most common types of thermal analysis are: Differntail scanning calorimetry (DSC) Differential thermal analysis (DTA), Thermogravimetric analysis (TGA) Thermomechanical analysis (TMA).
  • 14. Polymorphism • Some elements like carbon (Dimond, graphite) and sulphur exist in more than one crystalline form which is known as polymorphism • Diamond is metastable (less stable) form of carbon • Polymorphs exhibit different- • Melting points • Solubility • Formation of different polymorphs depend upon crystallization conditions (Level of supersaturation, temperature)
  • 15. Pharmaceutical significance of polymorphs • Nearly all long chain organic compounds exhibit polymorphism • Eg: Triglyceride tristearin shows • Low melting point metastable (α) • Beta prime (β’) • High melting point Stable beta (β) • Theobroma (coca butter) shows 4 forms γ, α, β’ and β. For making suppositories Theobroma should be melted at lowest possible temperature (33C) so that stable polymorph (β MP 34.5C)) should not destroy. • Because of difference in solubilities of polymorphs, one may be more active therapeutically than other. E.g. Sulfameter antimicrobial form II is more active than Form III. • Cortisone acetate suspension … out of 5 forms only one is stable in presence of water. During preparation of suspension stable form should be available to avoid caking.
  • 16. References Sinko, P. J. Martin's physical pharmacy and pharmaceutical sciences: physical chemical and biopharmaceutical principles in the pharmaceutical sciences, Philadelphia, Lippincott Williams & Wilkins.