Type of adsorption- Pharmaeutical Physical ChemistrySanchit Dhankhar
Adsorption
Adsorption versus absorption, Desorption
Types of adsorption: Physisorption and Chemisorption
Factors affecting adsorption
Adsorption isotherms: Freundlich and Langmuir
Gibbs adsorption isotherm
Bet equation and its use in surface area determination
Applications
ADSORPTION
Adsorption is the process in which matter is extracted from one phase and concentrated at the surface of a second phase. (Interface accumulation). This is a surface phenomenon as opposed to absorption where matter changes solution phase, e.g. gas transfer. This is demonstrated in the following schematic.
Type of adsorption- Pharmaeutical Physical ChemistrySanchit Dhankhar
Adsorption
Adsorption versus absorption, Desorption
Types of adsorption: Physisorption and Chemisorption
Factors affecting adsorption
Adsorption isotherms: Freundlich and Langmuir
Gibbs adsorption isotherm
Bet equation and its use in surface area determination
Applications
ADSORPTION
Adsorption is the process in which matter is extracted from one phase and concentrated at the surface of a second phase. (Interface accumulation). This is a surface phenomenon as opposed to absorption where matter changes solution phase, e.g. gas transfer. This is demonstrated in the following schematic.
Adsorption is the adhesion of molecules of gas, liquid, or dissolved solids to a surface. This process creates a film of the adsorbate (the molecules or atoms being accumulated) on the surface of the adsorbent. It differs from absorption, in which a fluid permeates or is dissolved by a liquid or solid.
Adsorption, types of adsorption, physisorption, chemisorption, mechanism of adsorption, Difference between adsorption and absorption, Factors affecting adsorption, applications of adsorption-
Gas masks
Adsorption indicators
Chromatographic separation
Removal of coloring matter
Heterogeneous catalysis
Controlling humidity
Curing diseases
Froth flotation process
Production of high vacuum
Purification,
adsorption equilibrium, adsorption isotherms, Langmuir isotherm- assumptions, Langmuir equation, limitations of Langmuir isotherm, equation, Freundlich isotherm- Assumptions of Freundlich Isotherm,Limitations of Freundlich Isotherm,Differences between Freundlich and Langmuir adsorption isotherms, BET isotherm-Drawbacks of BET adsorption theory, Types of BET adsorption isotherms, Differences between Langmuir and BET adsorption isotherm, Applications of BET isotherm, Why is Langmuir surface area always higher than BET surface area?
Temkin isotherm, D-R isotherms, Drawbacks of D-R Isotherm, Drawbacks of Temkin Isotherm, Uses of D-R isotherms, applications of adsorption isotherms -Spontaneity,
Exothermicity,
Percentage removal of adsorbate,
Langmuir parameters- maximum adsorbent uptake and affinity between adsorbent and adsorbate,Freundlich parameters- adsorption capacity of adsobents.
BET isotherms- specific surface area, pore size distribution curves
D-R parameters- adsorption mechanism
Temkin parameters- adsorbent-adsobate interactions
BET Surface Area Analysis of Nanoparticles.pptxNiveenIbrahim3
The BET theory was developed by Stephen Brunauer, Paul Emmett, and Edward Teller in 1938. The first letter of each publisher’s surname was taken to name this theory. The BET theory was an extension
of the Langmuir theory, developed by Irving Langmuir.
The specific surface area of a powder is determined by the physical adsorption of a gas on the solid's surface and by the calculating the amount of adsorbate gas corresponding to a monomolecular layer on the surface. The physical adsorption result from relatively weak van der Waals forces between the adsorbate gas molecules and the adsorbent surface area of the test powder. Usually, the determination is performed at the temperature of liquid nitrogen. Typically the amount of gas adsorbed is measured by a volumetric or continuous flow procedure.
Adsorption is the adhesion of molecules of gas, liquid, or dissolved solids to a surface. This process creates a film of the adsorbate (the molecules or atoms being accumulated) on the surface of the adsorbent. It differs from absorption, in which a fluid permeates or is dissolved by a liquid or solid.
Adsorption, types of adsorption, physisorption, chemisorption, mechanism of adsorption, Difference between adsorption and absorption, Factors affecting adsorption, applications of adsorption-
Gas masks
Adsorption indicators
Chromatographic separation
Removal of coloring matter
Heterogeneous catalysis
Controlling humidity
Curing diseases
Froth flotation process
Production of high vacuum
Purification,
adsorption equilibrium, adsorption isotherms, Langmuir isotherm- assumptions, Langmuir equation, limitations of Langmuir isotherm, equation, Freundlich isotherm- Assumptions of Freundlich Isotherm,Limitations of Freundlich Isotherm,Differences between Freundlich and Langmuir adsorption isotherms, BET isotherm-Drawbacks of BET adsorption theory, Types of BET adsorption isotherms, Differences between Langmuir and BET adsorption isotherm, Applications of BET isotherm, Why is Langmuir surface area always higher than BET surface area?
Temkin isotherm, D-R isotherms, Drawbacks of D-R Isotherm, Drawbacks of Temkin Isotherm, Uses of D-R isotherms, applications of adsorption isotherms -Spontaneity,
Exothermicity,
Percentage removal of adsorbate,
Langmuir parameters- maximum adsorbent uptake and affinity between adsorbent and adsorbate,Freundlich parameters- adsorption capacity of adsobents.
BET isotherms- specific surface area, pore size distribution curves
D-R parameters- adsorption mechanism
Temkin parameters- adsorbent-adsobate interactions
BET Surface Area Analysis of Nanoparticles.pptxNiveenIbrahim3
The BET theory was developed by Stephen Brunauer, Paul Emmett, and Edward Teller in 1938. The first letter of each publisher’s surname was taken to name this theory. The BET theory was an extension
of the Langmuir theory, developed by Irving Langmuir.
The specific surface area of a powder is determined by the physical adsorption of a gas on the solid's surface and by the calculating the amount of adsorbate gas corresponding to a monomolecular layer on the surface. The physical adsorption result from relatively weak van der Waals forces between the adsorbate gas molecules and the adsorbent surface area of the test powder. Usually, the determination is performed at the temperature of liquid nitrogen. Typically the amount of gas adsorbed is measured by a volumetric or continuous flow procedure.
A Method For Evaluating the Sorption Capacity of The SorbentsIJMERJOURNAL
ABSTRACT: A new method for evaluating the sorption capacity of the sorbents is offered. The proposed model is based on the adsorption data of the sorbent depending on the sorption duration in static mode. The new model allows to quickly and easily evaluate the duration of sorbent saturation. The formula of this relationship is determined by means of plotting of sorbent saturation curve on the base of experimental data, and using of Exel Trendline program. After the appropriate calculations and plotting q from time the sorption capacity of the sorbent is estimated. The model, as a primary parameter, includes time. The experimental data were obtained on the base of peat-containing sorbent for sorption of copper and cobalt. Sorption processes were evaluated by ICP-MS.
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Climate Impact of Software Testing at Nordic Testing DaysKari Kakkonen
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Climate impact / sustainability of software testing discussed on the talk. ICT and testing must carry their part of global responsibility to help with the climat warming. We can minimize the carbon footprint but we can also have a carbon handprint, a positive impact on the climate. Quality characteristics can be added with sustainability, and then measured continuously. Test environments can be used less, and in smaller scale and on demand. Test techniques can be used in optimizing or minimizing number of tests. Test automation can be used to speed up testing.
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Isotherms
1. Isotherms
Adsorption is usually described through isotherms, that is, the amount of adsorbate on the
adsorbent as a function of its pressure (if gas) or concentration (if liquid) at constant
temperature. The quantity adsorbed is nearly always normalized by the mass of the
adsorbent to allow comparison of different materials.
Freundlich
The first mathematical fit to an isotherm was published by Freundlich and Küster (1894)
and is a purely empirical formula for gaseous adsorbates,
where x is the quantity adsorbed, m is the mass of the adsorbent, P is the pressure of
adsorbate and k and n are empirical constants for each adsorbent-adsorbate pair at a
given temperature. The function has an asymptotic maximum as pressure increases
without bound. As the temperature increases, the constants k and n change to reflect the
empirical observation that the quantity adsorbed rises more slowly and higher pressures
are required to saturate the surface.
Langmuir
In 1916, Irving Langmuir published a new model isotherm for gases adsorbed to solids,
which retained his name. It is a semi-empirical isotherm derived from a proposed kinetic
mechanism. It is based on four assumptions:
1. The surface of the adsorbent is uniform, that is, all the adsorption sites are
equivalent.
2. Adsorbed molecules do not interact.
3. All adsorption occurs through the same mechanism.
4. At the maximum adsorption, only a monolayer is formed: molecules of adsorbate
do not deposit on other, already adsorbed, molecules of adsorbate, only on the
free surface of the adsorbent.
These four assumptions are seldom all true: there are always imperfections on the
surface, adsorbed molecules are not necessarily inert, and the mechanism is clearly not
the same for the very first molecules to adsorb to a surface as for the last. The fourth
condition is the most troublesome, as frequently more molecules will adsorb to the
monolayer; this problem is addressed by the BET isotherm for relatively flat (non-
microporous) surfaces. The Langmuir isotherm is nonetheless the first choice for most
models of adsorption, and has many applications in surface kinetics (usually called
Langmuir-Hinshelwood kinetics) and thermodynamics.
2. Langmuir suggested that adsorption takes place through this mechanism:
, where A is a gas molecule and S is an adsorption site. The direct and
inverse rate constants are k and k-1. If we define surface coverage, θ, as the fraction of the
adsorption sites occupied, in the equilibrium we have
or
Where P is the partial pressure of the gas or the molar concentration of the solution. For
very low pressures and for high pressures
θ is difficult to measure experimentally; usually, the adsorbate is a gas and the quantity
adsorbed is given in moles, grams, or gas volumes at standard temperature and pressure
(STP) per gram of adsorbent. If we call vmon the STP volume of adsorbate required to
form a monolayer on the adsorbent (per gram of adsorbent), and we obtain an
expression for a straight line:
Through its slope and y-intercept we can obtain vmon and K, which are constants for each
adsorbent/adsorbate pair at a given temperature. vmon is related to the number of
adsorption sites through the ideal gas law. If we assume that the number of sites is just
the whole area of the solid divided into the cross section of the adsorbate molecules, we
can easily calculate the surface area of the adsorbent. The surface area of an adsorbent
depends on its structure; the more pores it has, the greater the area, which has a big
influence on reactions on surfaces.
If more than one gas adsorbs on the surface, we define θE as the fraction of empty sites
and we have
and
3. where i is each one of the gases that adsorb.
BET
Often molecules do form multilayers, that is, some are adsorbed on already adsorbed
molecules and the Langmuir isotherm is not valid. In 1938 Stephen Brunauer, Paul
Emmett, and Edward Teller developed a model isotherm that takes that possibility into
account. Their theory is called BET theory, after the initials in their last names. They
modified Langmuir's mechanism as follows:
A(g) + S ⇌ AS
A(g) + AS ⇌ A2S
A(g) + A2S ⇌ A3S and so on
Langmuir isotherm (red) and BET isotherm (green)
The derivation of the formula is more complicated than Langmuir's (see links for
complete derivation). We obtain:
x is the pressure divided by the vapor pressure for the adsorbate at that temperature
(usually denoted P / P0
), v is the STP volume of adsorbed adsorbate, vmon is the STP
volume of the amount of adsorbate required to form a monolayer and c is the equilibrium
constant K we used in Langmuir isotherm multiplied by the vapor pressure of the
adsorbate. The key assumption used in deriving the BET equation that the successive
heats of adsorption for all layers except the first are equal to the heat of condensation of
the adsorbate.
The Langmuir isotherm is usually better for chemisorption and the BET isotherm works
better for physisorption for non-microporous surfaces.
Kisliuk
4. Two adsorbate nitrogen molecules adsorbing onto a
tungsten adsorbent from the precursor state around
an island of previously adsorbed adsobate (left) and
via random adsorption (right)
In other instances, molecular interactions between
gas molecules previously adsorbed on a solid surface form significant interactions with
gas molecules in the gaseous phase. Hence, adsorption of gas molecules to the surface is
more likely to occur around gas molecules that are already present on the solid surface,
rendering the Langmuir adsorption isotherm ineffective for the purposes of modelling.
This effect was studied in a system where nitrogen was the adsorbate and tungsten was
the adsorbent by Paul Kisliuk (b. 1922-d. 2008) in 1957. To compensate for the increased
probability of adsorption occurring around molecules present on the substrate surface,
Kisliuk developed the precursor state theory, whereby molecules would enter a precursor
state at the interface between the solid adsorbent and adsorbate in the gaseous phase.
From here, adsorbate molecules would either adsorb to the adsorbent or desorb into the
gaseous phase. The probability of adsorption occurring from the precursor state is
dependent on the adsorbate’s proximity to other adsorbate molecules that have already
been adsorbed. If the adsorbate molecule in the precursor state is in close proximity to an
adsorbate molecule which has already formed on the surface, it has a sticking probability
reflected by the size of the SE constant and will either be adsorbed from the precursor
state at a rate of kEC or will desorb into the gaseous phase at a rate of kES. If an adsorbate
molecule enters the precursor state at a location that is remote from any other previously
adsorbed adsorbate molecules, the sticking probability is reflected by the size of the SD
constant.
These factors were included as part of a single constant termed a "sticking coefficient,"
kE, described below:
As SD is dictated by factors that are taken into account by the Langmuir model, SD can be
assumed to be the adsorption rate constant. However, the rate constant for the Kisliuk
model (R’) is different to that of the Langmuir model, as R’ is used to represent the
impact of diffusion on monolayer formation and is proportional to the square root of the
system’s diffusion coefficient. The Kisliuk adsorption isotherm is written as follows,
where Θ(t) is fractional coverage of the adsorbent with adsorbate, and t is immersion time:
Solving for Θ(t) yields:
5. Henderson-Kisliuk
The Henderson-Kisliuk adsorption equation
prediction of normalised impedance as a function of
adsorption time, where the first peak corresponds to
the formation of an adsorbent surface that is saturated
with MPA in its "lying down" structure. The curve
then tends to an impedance value that is
representative of an adsorbent saturated with
"standing up" structure.
This adsorption isotherm was developed for use with the new field of Self Assembling
Monolayer (SAM) adsorption. SAM molecules adsorb to the surface of an adsorbent until
the surface becomes saturated with the SAM molecules' hydrocarbon chains lying flat
against the adsorbate. This is termed "lying down" structure (1st structure). Further
adsorption then occurs, causing the hydrocarbon chains to be displaced by thiol groups
present on the newly adsorbed SAM molecules. When this adsorption step takes place,
electrostatic forces between the newly adsorbed SAM molecules and the ones previously
adsorbed, causes a new structure to form, where all of the SAM molecules are occupying
a "standing up" orientation (2nd structure). As further adsorption takes place, the entire
adsorbent becomes saturated with SAM in a standing up orientation, and no further
adsorption takes place.
The SAM adsorbate is usually present in a liquid phase and the adsorbent is normally a
solid. Hence, intermolecular interactions are significant and the Kisliuk adsorption
isotherm applies. The sequential evolution of "lying down" and "standing up"
mercaptopropionic acid (MPA) SAM structures on a gold adsorbent, from a liquid MPA-
ethanol adsorbate phase, was studied by Andrew P. Henderson (b. 1982) et al. in 2009.
Henderson et al. used electrochemical impedance spectroscopy to quantify adsorption
and witnessed that the 1st structure had different impedance properties to the 2nd
structure and that both structures evolved sequentially. This allowed four rules to be
expressed:
• That the amount of adsorbate on the adsorbent surface was equal to the sum of the
adsorbate occupying 1st structure and 2nd structure.
• The rate of 1st structure formation is dependent on the availability of potential
adsorption sites and intermolecular interactions.
• The amount of 1st structure is depleted as 2nd structure is formed.
6. • The rate of second structure formation is dictated by the amount of adsorbate
occupying 1st structure and intermolecular interactions at immersion time, t.
From these statements, Henderson et al. used separate terms to describe rate of fractional
adsorption for 1st structure [Θ1(t)] and 2nd structure [Θ2(t)] as a function of immersion time
(t). Both of these terms were dictated by the Kisliuk adsorption isotherm, where variables
with a subscript of 1 relate to 1st structure formation and a subscript of 2 relates to 2nd
structure formation.
These terms were combined in the Henderson adsorption isotherm, which determines the
total normalised impedance detection signal strength caused by the adsorbate monolayer
(z(t)) as a function of Θ1(t), Θ2(t), φ1 and φ2. Values of φ are weighting constants, which are
normalized signal values that would result from an adsorbent covered entirely with either
1st structure or 2nd structure. This isotherm equation is shown below:
Although the Henderson-Kisliuk adsorption isotherm was originally applied to SAM
adsorption, Henderson et al. hypothesised that this adsorption isotherm is potentially
applicable to many other cases of adsorption and that Θ1(t) and Θ2(t) can be calculated
using other adsorption isotherms, in place of the Kisliuk model (such as the Langmuir
adsorption isotherm equation).
Adsorption enthalpy
Adsorption constants are equilibrium constants, therefore they obey van 't Hoff's
equation:
As can be seen in the formula, the variation of K must be isosteric, that is, at constant
coverage. If we start from the BET isotherm and assume that the entropy change is the
same for liquefaction and adsorption we obtain ΔHads = ΔHliq − RTlnc, that is to say,
adsorption is more exothermic than liquefaction.
7. • The rate of second structure formation is dictated by the amount of adsorbate
occupying 1st structure and intermolecular interactions at immersion time, t.
From these statements, Henderson et al. used separate terms to describe rate of fractional
adsorption for 1st structure [Θ1(t)] and 2nd structure [Θ2(t)] as a function of immersion time
(t). Both of these terms were dictated by the Kisliuk adsorption isotherm, where variables
with a subscript of 1 relate to 1st structure formation and a subscript of 2 relates to 2nd
structure formation.
These terms were combined in the Henderson adsorption isotherm, which determines the
total normalised impedance detection signal strength caused by the adsorbate monolayer
(z(t)) as a function of Θ1(t), Θ2(t), φ1 and φ2. Values of φ are weighting constants, which are
normalized signal values that would result from an adsorbent covered entirely with either
1st structure or 2nd structure. This isotherm equation is shown below:
Although the Henderson-Kisliuk adsorption isotherm was originally applied to SAM
adsorption, Henderson et al. hypothesised that this adsorption isotherm is potentially
applicable to many other cases of adsorption and that Θ1(t) and Θ2(t) can be calculated
using other adsorption isotherms, in place of the Kisliuk model (such as the Langmuir
adsorption isotherm equation).
Adsorption enthalpy
Adsorption constants are equilibrium constants, therefore they obey van 't Hoff's
equation:
As can be seen in the formula, the variation of K must be isosteric, that is, at constant
coverage. If we start from the BET isotherm and assume that the entropy change is the
same for liquefaction and adsorption we obtain ΔHads = ΔHliq − RTlnc, that is to say,
adsorption is more exothermic than liquefaction.