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Gaseous and Liquid State

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    Gaseous and Liquid state

    Thus matter is classified mainly into three categories depending upon its physical state namely solid,

    liquid and gaseous states.

    Distinction between three states of matter:

    S.No Property Solid Liquid Gas

    1 Shape Definite shape Indefinite shape Indefinite shape

    2 Volume Definite Volume Definite Volume Indefinite Volume

    3 Inter particular

    Forces

    Strong Inter

    particular Forces

    Comparatiely !ea"er Inter

    particular Forces

    Inte rparticular force

    negligi#le

    $ Inter particular

    Space

    %egligi#le inter

    particular space

    Comparatiely large inter

    particular space

    Very large Inter part

    space

    & 'articular (otion 'article motion is

    restricted to i#ratory

    motion.

    'article motion is ery slo! 'article motion is e

    and also random.

    ) 'ac"ing of

    'articles

    'articles are ery

    Closely pac"ed

    'articles are loosely pac"ed 'articles are ery lo

    pac"ed

    * Compressi#ility Incompressi#le Compressi#le +ighly Compressi#le

    Density Very +igh Density -o! Density Very lo! density

    Parameters of GasesThe characteristics of gases are described in terms of following four

    parameters

    (ass

    Volume

    'ressure

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    Temperature

    1. Mass (m):

    The mass of the gas is related to the number of moles as

    n = w/M

    Where n = number of moles

    w = mass of gas in grams

    M = molecular mass of the gas

    2. Volume (V):

    Since gases occupy the entire space available to them, therefore the gas

    volume means the volume of the container in which the gas is enclosed.

    Units of Volume: Volume is generally epressed in litre (L), cm !!m

    1m" 1#litre " 1#!m" 1#$cm.

    . Pressure:

    "ressure of the gas is due to its collisions with walls of

    its container i.e. the force eerted by the gas per unit area on the walls

    of the container is e#ual to its pressure.

    "ressure is eerted by a gas due to $inetic energy of its molecules.

    %s temperature increases, the $inetic energy of molecules increases, which

    results in increase in pressure of the gas. So, pressure of any gas is

    directly proportional to its temperature.

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    Units of Pressure:

    The pressure of a gas is epressed inatm, Pa, %m&2, bar andlb'n2 (si).

    &'( mm = ) atm = )()*+. -"a= )()*+ "a= )()*+ m+

    &'( mm of 0g = ).()*+ bar = )()*.+ milli bar = )1.& lb/+n+2psi3

    . *emerature (*):

    Temperature is defined as the degree of hotness. The S4 unit of

    temperature is -elvin. o5 and o6 are the two other units used for

    measuring temperature. 7n the 5elsius scale water free8es at (95 and boils

    at )((95 where as in the -elvin scale water free8es at +&* - and boils at

    *&* -.

    + " o - 2./

    0 " ('/) o - 2

    Gas Laws:1. o3le4s Law:5

    At constant temperature, the pressure of a fixed amount

    (i.e., number of moles n) of gas varies inversely with its

    volume.

    Grahical 6eresentation of o3le4s

    Law :

    plot of P ersus /0V at constant temperature for a fi1ed mass of gas !ould #e a straight

    line passing through the origin.

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    plot of Persus Vat constant temperature for a fi1ed mass of a gas !ould #e a rectangular

    hyper#ola.

    plot of P (or V ersus PVat constant temperature for a fi1ed mass of a gas is a straight

    line parallel to the PV axis.

    2. Charles Law:-

    At constant pressure, the volume of a given mass of a gas

    is directly proportional to its absolute temperature

    or

    Grahical 6eresentation of harles4s

    Law :

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    ). 6or a definite mass of the gas a plot of Vvs T2o-3 at constant

    pressure is a straight line passing through the origin.

    +. % plot of V vs t2o53 at constant pressure is a straight line cutting

    the temperature ais at :+&* o5

    3. Combined Gas Law:-

    This la! states that at constant volume, the pressure of a given mass of a gas is directly

    proportional to its absolute temperature.

    the com#ination of 4oyle5s -a! and Charles5 -a!6

    . Gay Lussa!s Law:

    Where,

    P" Pressure of Gas

    T" 7bsolute *emerature

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    4f the pressure and temperature of a gas changes from P)! T1to P2! T2 ,

    volume remaining constant , we have

    where,

    "t= "ressure of gas at t o5

    "o = "ressure of gas at ( o5

    t = Temperature in o5.

    Grahical 6eresentation of Ga35Lussac4s Law

    ". #$o%adro Law:

    Samples of different gases which contain the same number of molecules

    (any complexity si!e shape" occupy the same #olume at the same

    temperature and pressure$.

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    4t follows from %vogadro;s hypothesis that 2when T and " are

    constant3.

    Mathematicall3

    &. 'deal Gas (quation:

    Ideal gas o#ey all the three la!s i.e. 4oyle5s, Charles5s, and ogadro7s la! strictly.

    p 8 n9T

    :here,

    where < is the constant of proportionality or universal gas constant

    The value of < was found out to be

    < = .*)1 > mol)-)

    < = (.(+) litre atm -)mol)

    < = + cal -)mol)

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    Ideal gas equation is also "no!n as equation ofstate.

    ). *altons law o+ partial pressures:

    The total pressure of mi1ture of non;reactie gases at constant temperature and pressure is equal to

    the sum of the indiidual partial pressures of the gases.

    ptotal 8 p/

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    The aerage "inetic energy of the particles of a gas is directly proportional to the a#solute

    temperature.

    'ressure of the gas is due to the collision #et!een gas molecules and !alls of the container.

    *he +inetic 8uation

    Velocities of 9as molecules

    #$era%e ,elo!ity

    %verage velocity =

    oot ean Square ,elo!ity:-

    Mawell proposed the term Drmsas the s#uare root of means of s#uare of all

    such velocities.

    also

    ost probable $elo!ity:-

    4t is the velocity which is possessed by maimum no. of molecules.

    6urthermore

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    +inetic 8ner93 of Gas

    %s per $inetic e#uation

    6or ) mole m E n = Molecular Mass 2M3

    %lso

    Where $ is the Folt8mann constant 2$ = < / 3

    Graham4s Law of Diffusion'8ffusion:

    /. *i++usion:a#ility of a gas to spread and occupy the !hole aaila#le olume irrespectie of other gases

    present in the container

    2. (++usion:process #y !hich a gas escapes from one cham#er of a essel through a small opening or

    an orifice

    r ) / Gd

    where r is the rate of diffusion and d is the density of the gas.

    ow, if there are two gases % and F having r )and r+as their rates of diffusion

    and d)and d+their densities respectively. Then

    r) )

    and

    r+

    or

    ,

    The rate of diffusion @r of a gas at constant temperature is directly preoperational to its pressure

    De;iation from i!eal 9as beha;ior:

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    0or ideal %as1

    Compressi#ility factor i.e. A 8 'V0n9T 8/

    For non;Ideal gas, A B/

    Thus for non;ideal gas,A can #e / or /

    hen 4 /, it is a negatie deiation. It sho!s that the gas is more compressi#le than e1pected

    from ideal #ehaiour.

    hen 5 /, it is a positie deiation. It sho!s that the gas is less compressi#le than e1pected from

    ideal #ehaiour.

    /. Causes o+ de$iation +rom ideal beha$iour:

    The olume occupied #y gas molecules is negligi#ly small as compared to the olume occupied #y

    the gas.

    The forces of attraction #et!een gas molecules are negligi#le.

    2. ,an der waals (quation:

    :here,

    a and # are an der !aals

    constants.

    t lo! pressures6

    'V 8 9T > a0V

    or

    'V 9TThis accounts for the dip in 'V s '

    isotherm at lo! pressure

    #t +airly hi%h pressures

    a0V2 may #e neglected in comparison !ith '. The Vander :aals equation #ecomes

    'V 8 9T < '#

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    or

    'V 9T

    This accounts for the rising parts of the 'V s ' isotherm at high pressures

    6oyles 7emperature 87b9 :-temperature at !hich real gas o#eys the gas la!s oer a !ide range of

    pressure.

    T#8 a 0 9# 8 /02 T/

    Liuefaction of 9ases:

    Criti!al temperature 87!9:- temperature at !hich a gas liquefies. Tc8 a 0 2*9#

    Criti!al ,olume: 8,!9 :-olume of one mole of a gas at critical temperature.Vc8 3#

    Criti!al pressure 8p!9:-pressure of gas at its critical temperature. 'c8 a02*#2

    olar heat !apa!ity o+ ideal %ases:-the amount of heat required to raise the temperature of /

    mole of a gas trough /EC.

    5":5V= < !

    "oissonHs ratio 2I3 = 5"/5V

    6or monatomic gas 5p= cal and 5v=* cal

    I = /* = ).'&

    6or diatomic gas 5p= & cal and 5v= cal

    I =&/ = ).1

    6or polyatomic gas 5p= cal and 5v= cal

    I = /' = ).**

    %lso 5p= 5pm,

    Where, 5pand 5vare specific heat and m, is molecular weight.

    Liui!

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    Surface tension @ 8 :or" done 0 Change in area

    Gnits6 CGS:dcm;/

    S': %m;/

    The surface of the liquid tends to contract to the smallest possi#le

    area for a gien olume of the liquid i.e. spherical shape.Surface Tension of liquid decreases !ith increase of temperature

    and #ecomes Hero at its critical temperature.

    Sur+a!e 7ension in e$eryday li+e:

    Cleansing action of soap and detergents.

    fficacy of tooth pastes, mouth !ashes and nasal Jellies.

    ,is!osity:

    It is the force of friction !hich one part of the liquid offers to another part of the liquid.

    Coefficient of iscosity6 is the force per unit area required to maintain unit difference of elocity

    #et!een t!o parallel layers in the liquid one unit apart.

    Gnits6CGS:dscm;/

    S.': %sm;/

    Viscosity of liquid decreases !ith increase in temperature.


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