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1Glossarysolublea.可溶的insolublea.不溶的solubilityn.溶解度soluten.溶質(zhì)dissolublea.可溶解的dissolutionn.溶解dissociatev.離解dissociationn.離解作用ioniccompounds
n.離子型化合物electrolyte電解質(zhì)precipitaten.沉淀homogeneousa.均相的,均勻的heterogeneousa.異相的,不均勻的heterogeneousequilibria異相平衡theSolubility-ProductConstant溶度積常數(shù)reactionquotient
反應(yīng)商2PbCl2
LeadchlorideAgClSilverchlorideAgBrSilverbromideAg2CrO4
SilverchromateAg2SSilversulfideAgNO3silvernitrate
CaSO4CalciumsulfateBaSO4BariumsulfateHClhydrochloricacidH2SO4sulphuricacidHNO3Nitricacidgramlitermolemolarmolarsolubility3Chapter5EquilibriaofSlightlySolubleIonicCompounds
Aimstosolvetwoissues:ThecharacteristicsoftheequilibriumTheshiftoftheequilibrium4AgNO3(aq)+NaCl(aq)=AgCl(s)+NaNO3(aq)5
SlightlySolubleThereisnostandardruleforthesolubilityvalue.InsolublemeansS<0.1g/100gH2O,AgCl,AgBr,AgI,BaSO4
Slightlysoluble:S=0.1~1g/100gH2O,PbCl2CaSO4,Hg2SO4etc.
SolublemeansS>1g/100gH2OIonicCompounds
arestrongelectrolyteswhichdissociatecompletelyinaqueoussolution.
61TheCharacteristicsofEquilibriaofSlightlySolubleIonicCompounds1-1.TheCharacteristics:heterogeneousequilibriaBaSO4(s)
Ba2+(aq)+SO42-(aq)Makingtheassumptionofcompletedissociation,wecanstatethatforslightlysolubleioniccompounds,equilibriumexistsbetweensolidsoluteanddissolvedions.7
1-2.
TheSolubility-ProductConstant----Ksp(溶度積常數(shù))BaSO4(s)
Ba2+(aq)+SO42-(aq)teSSKsp=[Ba2+][SO42-]=S2GenerallyAmBn
mAn++nBm-temSnSKsp=[An+]m[Bm-]n
=[mS]m[nS]n
=mmnnSm+n81-3.ComparisonofKspandS(molarsolubility)
Table1.KspandSofsomeIonicCompoundsCompositionpatternMolecularFormulaKsp
S(mol/L)ABAgCl1.8
10-10
1.3
10-5
ABAgBr5.0
10-13
7.1
10-7
A2BAg2CrO42.0
10-12
7.9
10-5
A2BAg2S6.7
10-502.6
10-17
Formoleculeswiththesamepattern,thehigheritsKsp,thehigheritsS.Formoleculeswithdifferentpatterns,higherKspdoesn’tmeanhigherS.9Thesolubility-productKspandthemolarsolubilityS,bothexpressthesolubleabilityofacompound.Asformoleculeswiththesamepattern,thehigheritsKsp,thehigheritsS.Butformoleculeswithdifferentpatterns,higherKspdoesn’tmeanhigherS.AnotherpointisthattheKspisafunctionofthetemperature,ithasnothingtodowithions’concentrations,whileSchangeswiththeions’concentrations.10Example1:CalculatesolubilityofAgCl.Ksp=1.8
10-10(a)
In1Lwater.(b)
In0.01MHCl(c)In0.01MKNO3.
Solution:(a)AgCl(s)
Ag++Cl-teSSKsp=S2
S=
Ksp=1.3
10-5M11Example1:CalculatesolubilityofAgCl.Ksp=1.8
10-10(a)
In1Lwater.S=1.3
10-5mol/L(b)
In0.01mol/LHCl.(c)In0.01mol/LKNO3.
(b)
AgCl(s)
Ag++Cl-teSS+0.01
0.01Ksp=0.01S
S=1.8
10-8mol/L
(c)
I=0.01mol/L,lgf=-0.509
z+z-
If=0.89AgCl(s)
Ag++Cl-te0.89S0.89SKsp=(0.89S)2,S=1.46
10-5mol/L
12Example1:CalculatesolubilityofAgCl.Ksp=1.8
10-10(a)
In1Lwater.S=1.3
10-5mol/L(b)
In0.01mol/LHCl.S=1.8
10-8mol/L(c)In0.01mol/LKNO3.S=1.46
10-5mol/L
CommonIonEffectThepresenceofacommoniondecreasesthesolubilityofaslightlysolubleioniccompound.ASaltEffectisanincreaseinsolubilitycausedbythepresenceionsthatarenotcommonions.13142.
Theshiftoftheequilibrium----Predictingtheformation/dissolutionofaprecipitateQvs.KspT----Since
Hissmall;KspchangesslightlywithT;C152-1.TheLawofSolubility-Product
G=
G
+RTlnQsp=-RTlnKsp+RTlnQsp
Qsp----ion-product,whoseexpressionisidenticaltothesolubility-productexpression.
G<0,Qsp>Ksp
,netforwardreactionwilltakeplace(precipitateformsuntilsolutionissaturated).
G=0,Qsp=Ksp
,nonetchangewilltakeplace,systemisatequilibrium(solutionissaturated).
G>0,Qsp<Ksp
,netreversereactionwilltakeplace(solutionisunsaturatedandnoprecipitateforms).162-2
DissolutionofaPrecipitateTherearethreemethods:Toformweakacids/basesEg.CaCO3(s)+2H+=Ca2++CO2+H2O
ToformcomplexEg.AgCl(s)+2NH3·H2O=Ag(NH3)2++Cl-
Tocarryoutanoxidation-reductionreaction
CuS(s)+4H++2NO3-=Cu2++2NO2↑+S+2H2O17Example2:P401eg.10-15Twoormoretypesofionicequilibriaexistsimultaneously----
simultaneousequilibria
182-3.PredictingwhetheraprecipitatewillformSolution:[Ca2+]=0.30
0.100/(0.100+0.200)=0.10M[F-]=0.060
0.200/0.300=0.040MQ=[Ca2+][F-]2=0.10
0.0402=1.6
10-4>Ksp(CaF2)
CaF2willprecipitate.Example3:Acommonlaboratorymethodforpreparingaprecipitateistomixsolutionsofthecomponentions.Doesaprecipitateformwhen0.100Lof0.30MCa(NO3)2ismixedwith0.200Lof0.060MNaF?Ksp(CaF2)=3.2
10-1119SomepracticalapplicationsofsolubilityequilibriaThestandardforanionprecipitatecompletely:
c<1.0
10-6
mol/L(Quantitative)c<1.0
10-5
mol/L(Qualitative)SeparatingIonsbySelectivePrecipitate
202-4.ApplicationsofIonicEquilibriatoChemicalAnalysisSeparatingIonsbySelectivePrecipitate
21Example4:Asolutionconsistsof0.2MMgCl2and0.10MCuCl2.
Howwouldyouseparatethemetalionsastheirhydroxides?KspMg(OH)2=6.3
10-10,Ksp
Cu(OH)2=2.2
10-20.Solution:Whencopperionisfullyprecipitated,the[OH-]is:[OH-]2=Ksp
Cu(OH)2/[Cu2+]=2.2
10-20/1.0
10-6=2.2
10-14[OH-]=1.5
10-7MAtthismoment,theQofMg(OH)2is:Q=[Mg2+][OH-]2=0.2
(1.5
10-7)2=4.5
10-15
<KspMg(OH)2=6.3
10-10Thatistosay,virtuallyalltheCu2+ionwouldbeprecipitated,whiletheMg2+ionwillnotprecipitate(remaininsolution).
222.5Theconversionoftheprecipitate
Example5:BaCO3(s)+CrO42-
BaCrO4(s)+CO32-
Solution:K=[CO32-]/[CrO42-]=Ksp
BaCO3/KspBaCrO
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