Pure Substance o.uk c . e l A substance that has a fixed chemical composition a s e t o N throughout is called a pure substance, e.g.: H2O, 5 m 5 o r f f o w 4 e e N2, COr2evi g a P P A pure substance does not have to be of a single chemical element or compound A mixture of chemical elements/compounds also qualifies as a pure substance as long as the mixture is homogeneous, e.g. Air However, a mixture of oil and water is oil not a pure substance - oil is not homogeneous/soluble in water, forming water two chemically dissimilar regions Phases Of Pure Substances o.uk c . e l a s e t o having a distinct molecular N A phase is identified as 5 m 5 o r f f is 6homogeneous o arrangement that throughout and w e i e separated the others by easily identifiable Pag Prev from boundary surfaces. Eg: Two phases of water in iced water Three principal phases: solid, liquid and gas A substance may have several phases within a principal phase, each with a different molecular structure. For eg: Helium has two liquid phases; Iron has three solid phases. PROCESS 4-5 k u . o le.c a s e t o N 5 m 5 o f r f o 0 w 1 e i e v g e r a P P Tsat Properties of water in the superheated region listed in Superheated Tables v2=vf v4=vg k u . o le.c a s e t o N 5 m 5 o f r f o 4 w 1 e i e v g e r a P P Rajah 5 • Above critical temperature and pressure no significant process of phase change occurs. • The volume continues to increase and only one phase that similar to vapour phase exists. Quality and saturated region k .u o c . e l exists in two phases (liquid a s During vaporization, a substance e ot N 5 and vapour) that consists of af mixture of saturated liquid and m 5 o r f The 2ratio o of vapor to the total mass of 2 w saturated vapour. e i e v g e r a P mixture is quality.P x x=0 mvapour mtotal mvapour mliquid mvapour mg m f mg (or 0%) for saturated liquid and x=1 (or 100%) for saturated vapour, so the range for quality is 0 x 1. Quality has significance for saturated mixtures only. It has no meaning in the compressed liquid or superheated vapor regions. The properties of the saturated liquid are the same whether it exists alone or in a mixture with saturated vapor. During the vaporization process, only the amount of saturated liquid changes, not its properties. Similarly to a saturated vapor. Example of compressed liquid table k u . o le.c a s e t o N 5 m 5 o f r f o 8 w 2 e e The formatre ofvi g a P P Table 1–7 is similar to the superheated vapor tables, except the saturated data represent the saturated liquid properties Tsat Example 2.1 k u . o le.c a s e t o this table Using Property Tables, complete for H2O: N 5 om 3 of 5 r f w 3 e i e v g e PrP (MPa) Pva(m3/kg) T (oC) Phase and Quality (a) 1.725 (b) 0.85 (c) 15 (d) (e) (f) (g) 0.227 400 0.001124 0.75 180 0.221 0.3879 0.25 100 0.095 150 The Compressibility Factor, Z k u . co . e l a s e t From the Generalized Compressibility Chart, o N 5 m 5 o f r fobservation o can be made : the following 3 w 4 e i e v g e r a P P pressures (P << 1), gases 1.) At very low R behave as an Ideal Gas regardless of Temperature. 2.) At high temperatures (TR > 2), Ideal Gas behaviour can be assumed with good accuracy regardless of Pressure except when PR>>1. 3.) The deviation of a gas from Ideal Gas behaviour is greatest in the vicinity of the Critical Point. INTERNAL ENERGY, ENTHALPY AND SPECIFIC k u . o HEATS OF SOLIDS AND LIQUIDS e.c l a s e t o N 5 A substance whose specific fvolume (or density) is constant m 5 o r f substance o - the specific volumes of solids 5 w incompressible 5 e i e v g e r a P P and liquids essentially remain constant during a process. The constant-volume and constant-pressure specific heats are identical for incompressible substances: CV CP C kJ kg.K Specific heat values for several common liquids and solids are given in Table A–3. The specific heats of incompressible substances depend on T only. Thus, internal energy of the incompressible substances: du CdT u Cave T2 T1 integratio n Enthalpy?? ???
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