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Summary Thermodynamics

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Pharmacy - physical pharmacy 1st semester Bullet points, key notes, images and diagrams

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  • June 6, 2023
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Physical Pharmacy

Lecture 1 Thermodynamics

Temperature Scale

 Kelvin (K) is used as an absolute temperature scale independent of the substance used
for reference
 Derived from ideal gas at a low pressure
 0K= no molecular motion
 Heat is the process of transferring energy as a result of temperature difference
 Temperature determines which way energy flows- from high to low

Ideal Gases

 Obeys the relation PV=nRT
 They don’t interact and occupy no volume

Partial Pressures

 Pj=ΣPA
 PA=XAP
 XA=nA/Σni
 Partial pressures of a mixture added together equal the total pressure of gases

Types of System

 Adiabatic= no heat transfer q=0
 Diathermal=heat transfer
 Isothermal= constant T
 Open system= energy and matter exchanged with the surroundings
 Closed system= energy exchanged but not matter with the surroundings
 Isolated system= energy and matter isn’t exchanged with the surroundings

Conservation of Energy

 U=total energy of a system
 Energy lost by the system=Energy gained by the surroundings (vice versa)
 Closed system U=ΔU=q+w
 Isolated ΔU=0 as q and w are constant
 Work is the process of moving against an opposing force and the energy transfer is
uniform
 ΔV=Vf-Vi
 When w=0 it’s free expansion
 When the pressure outside the system is slightly lower than the internal pressure-
maximum work takes place

Calorimetry

 qv=CΔT
 Burn known mass of substance to get known energy so ΔT=C
 Differential scanning calorimeter (DSC)
 DSC compares to reference sample but they’re heated the same so the energy change is
measured

State Functions

 State function- dependant on the physical state of the substance
 Path function- dependant on how the substance changed to a physical state (q and w)

, Lecture 2 Enthalpy

Enthalpy

 H=U+PV where P is constant
 Measures enthalpy changes- exothermic and endothermic (making bonds and breaking
bonds/ releasing energy and taking in energy)
 Measured at standard states and conditions 298K and 1 bar

Enthalpy Change of Formation

 Is the standard reaction enthalpy for the formation of a compound from its elements
under standard states and conditions
 Elements enthalpy=0

Enthalpy Change of Combustion

 Is the standard reaction enthalpy for complete oxidation of an organic compound to if
only C, H and O present and N2

Hess’s Law

 Any chemical reaction that is independent of path and any intermediate reactions may
occur. Its initial reactants and final products which determine either ΔH or ΔU
 The standard enthalpies of an overall reaction is the sum of the standard enthalpies of
the individual reactions into which a reaction may be divided.

Heat Capacity

 C=q/ΔT
 C is the measure of temperature change in a body produced by an increment of heat
 Either carried out at a constant volume or pressure
 Extensive property (2kg has 2x the heat capacity of 1kg)

Lecture 3 Entropy

Entropy

 The entropy of an isolated system increases in the course of a spontaneous change
 Degrees of disorder is related to the transfer of energy as heat
 Heat causes a change in orderliness whereas work has no effect
 At high temperatures a small increase in temperature has a very small effect on entropy
 Entropy change= products-reactants

Entropy at 0K

 Third law- a pure, perfect crystal at 0K has zero entropy


Lecture 4 Gibbs Free Energy

Free Energy

 At a constant temperature and pressure
 ΔG<0 it’s spontaneous
 Only changes in ΔG can be measured
 Gibbs energy of formation- ΔrGm=ΔG products-ΔG reactants
 ΔrGm of elements=0

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