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LabModuleReport

Experiment1

Eep.Prefermentweek1:2012/10/26

Prefermentweek2:2012/11/2

Labparter:

Manager:

RulongWu

SoftwareTechnician:

JeanHirshfeld

Chemist:

SaraFurgeson

MethodsandMaterials

Part1:SynthesizingSodiumFerrate

Tobeginwith,20mLofcommercialbleachwaspouredintoa50mLbeaker,whichinturnwasplacedwithamagneticstirringrodonastirplate.Then10gofNaOHpelletswereaddedtothebeakerandthestirplateturnedonandthesolutionstartedtomix.Thenusingapipette,0.50mLof0.30MFeClwasaddedtodissolvedNaOHsolution.Themixturewasstirredfor10minutesandcooleddownfor5minutes.

Asuctionfiltrationapparatuswasassembledandthesolutionwasfilteredsothatonlytheconcentratedsolutionofsodiumferrateremained.

Thevolumeofthesolutionwasthenmeasuredusingagraduatedcylinderandthesolutionpouredintoavialforlateruse.

Part2:CalculatethePercentYieldofFerrate

TheSpectraVisspectrometerwascalibratedusingDIwaterinfullspectrummode.TheDIwaterwasremovedthoroughlyusingaplasticpipetteandthesodiumferratewasputinitsplace.Theabsorbanceofthesodiumferrateat510nmwasrecorded;however,sincethevaluerecordeddidnotmeettherequirements,thesolutionwasdiluteduntilthevalueoftheabsorbancerecordedat510nmwasbeneath1.5.Whenthatlevelwasreached,anothersampleofthesolutionwastestedat510nmandanothervaluefortheabsorbancewasrecorded.

Theremainderofthesolutionwasplacedinanotherbeakerinpreparationforthenextphaseoftheexperiment.

TheconcentrationofferrateintheoriginalsolutionwascalculatedusingBeer’sLaw.

Thetwovaluesforconcentrationwereusedbytakingtheaverageofthetwotogettheexperimentalyieldoftheferrate.

Thisvalueoftheexperimentalyieldwascomparedtothetheoreticalyieldthatwascalculatedatthebeginningoftheexperiment.

Part3:PerformingtheReactionbetweenFerrateandDIatrizoic

equationforthereaction,foreverymoleofFeCl3used,onemoleofsodiumferrate(Na2FeO4)wouldbeproduced.

2FeCl3+3NaClO+10NaOH→2Na2FeO4+9NaCl+5H2O

Thereactionused0.50mLof0.30MFeCl3,andthefinalamountofferratesolutionwas19mL.Thetheroreticalyieldwascalculatedtobe0.00769M.

0.50mL*0.30mol/LFeCl3*1L/1000mL=0.00015mol

0.00015mol/19mL*1000mL/L=0.00789mol/L=0.00789M

Staringwith2.6mLofsolution,10mLofwaterwasaddedtodiluteit.It’sabsorbanceat510nmwas1.455,givingitaconcentrationof0.001265M.Anothersamplehadanabsorbanceof1.192at510nmandaconcentrationof0.001037M.UsingtheformulaV1C1=V2C2theoriginalconcentrationsofthesolutionswerecalculatedtobe0.00613Mand0.00502M.Theaveragebetweenthemwas0.00558M.Thiswasdividedbythetheoreticalyieldof0.00789Mgivinga70.7percentyield.

Calculatingconcentrationsofsamples

V1C1=V2C2

2.6mL*C1=12.6mL*0.001265M

C1=0.00613M

2.6mL*C1=12.6mL*0.001037M

C1=0.00502M

Averageoftwoconcentrations

(0.00613M+0.00502M)/2=0.00558M

Calculatingthepercentyield

(0.00558M/0.00789M)*100%=70.7%

Thereactionbetweenthosesolutionsof00558MferratewastimedasitreactedwithDTZA.Theabsorbancewasmeasuredasthetimedpassedtocalculatehowfastthereactionwastakingplaceandhowfasttheconcentrationwaschanging.Thenthisexperimentwasrepeatedatdifferenttemperaturestoseeifloweringthetemperaturewouldslowdownthereaction.Thetemperaturestestedwere1,4.8,12,and16degreesCelsius.AlltheratesofreactionweretakenfromFigures3through7andcompiledintoTable8andFigure8forcomparison.

Trial1:

Time(s)

ABS@510nm

FerrateConc.(M)

0

0.631

0.000548696

30

0.656

0.000570435

60

0.674

0.000586087

90

0.622

0.000540870

120

0.605

0.000526087

150

0.583

0.000506957

180

0.560

0.000486957

210

0.552

0.000480000

240

0.542

0.000471304

270

0.542

0.000471304

300

0.542

0.000471304

Table1:Thistableshowsthedifferencesinabsorbanceat510nmandconcentrationasthetimechangesforthefirsttrialofthereactionbetweenferrateandDTZA.

Figure1:ThisshowsthefirsttrialoftimedreactionbetweenferrateandDTZAandtherelatedequation.

Trial2:

Time(s)

ABS@510nm

FerrateConc.(M)

0

0.589

0.000512174

30

0.578

0.000502609

60

0.579

0.000503478

90

0.579

0.000503478

120

0.582

0.000506087

150

0.578

0.000502609

180

0.578

0.000502609

210

0.569

0.000494783

240

0.562

0.000488696

270

0.558

0.000485217

300

0.556

0.000483478

Table2:Thistableshowsthedifferencesinabsorbanceat510nmandconcentrationasthetimechangesforthesecondtrialofthereactionbetweenferrateandDTZA.

Figure2:ThisshowsthesecondtrialoftimedreactionbetweenferrateandDTZAandtherelatedequation.

Reactionsat1DegreeCelsius

Time(s)

ABS@510nm

FerrateConc.(M)

0

0.828

0.000720000

30

0.830

0.000721739

60

0.837

0.000727826

90

0.729

0.000633913

120

0.719

0.000625217

150

0.655

0.000569565

180

0.633

0.000550435

210

0.658

0.000572174

240

0.667

0.000580000

270

0.630

0.000547826

300

0.643

0.000559130

Table3:ThisshowsthesamereactionwhentheferrateandDZTAstartedat1degreeCelsius.Asthereactiontakesplace,absorbanceandconcentrationchangewithtime.

Figure3:Thisshowstherelationshipbetweenthetimeandtheconcentrationwhenthereactionstartedat1degreeCelsius.

Reactionsat4DegreesCelsius

Time(s)

ABS@510nm

FerrateConc.(M)

0

0.867

0.000753913

30

0.868

0.000754783

60

0.861

0.000748696

90

0.868

0.000754783

120

0.845

0.000734783

150

0.835

0.000726087

180

0.837

0.000727826

210

0.834

0.000725217

240

0.844

0.000733913

270

0.832

0.000723478

300

0.827

0.00071913

Table4:ThisshowsthesamereactionwhentheferrateandDZTAstartedat4degreesCelsius.Asthereactiontakesplace,absorbanceandconcentrationchangewithtime.

Figure4:Thisshowstherelationshipbetweenthetimeandtheconcentrationwhenthereactionstartedat4degreesCelsius.

Reactionsat8DegreesCelsius

Time(s)

ABS@510nm

FerrateConc.(M)

0

0.939

0.000816522

30

0.81

0.000704348

60

0.805

0.0007

90

0.809

0.000703478

120

0.816

0.000709565

150

0.793

0.000689565

180

0.822

0.000714783

210

0.812

0.000706087

240

0.806

0.00070087

270

0.816

0.000709565

300

0.793

0.000689565

Table5:ThisshowsthesamereactionwhentheferrateandDZTAstartedat8degreesCelsius.Asthereactiontakesplace,absorbanceandconcentrationchangewithtime.

Figure5:Thisshowstherelationshipbetweenthetimeandtheconcentrationwhenthereactionstartedat8degreesCelsius.

Reactionsat12DegreesCelsius

Time(s)

ABS@510nm

FerrateConc.(M)

0

0.647

0.000562609

30

0.635

0.000552174

60

0.91

0.000791304

90

0.847

0.000736522

120

0.817

0.000710435

150

0.839

0.000729565

180

0.802

0.000697391

210

0.807

0.000701739

240

0.776

0.000674783

270

0.78

0.000678261

300

0.803

0.000698261

Table6:ThisshowsthesamereactionwhentheferrateandDZTAstartedat12degreesCelsius.Asthereactiontakesplace,absorbanceandconcentrationchangewithtime.

Figure6:Thisshowstherelationshipbetweenthetimeandtheconcentrationwhenthereactionstartedat12degreesCelsius.Theconcentrationat0and30secondswaslowerthanallofthefollowingreadings.Therewasprobablysomeerror,sothesetwotimeswereignored.

Reactionsat16DegreesCelsius

Time(s)

ABS@510nm

FerrateConc.(M)

0

0.745

0.000647826

30

0.725

0.000630435

60

0.723

0.000628696

90

0.701

0.000609565

120

0.695

0.000604348

150

0.684

0.000594783

180

0.681

0.000592174

210

0.677

0.000588696

240

0.675

0.000586957

270

0.667

0.00058

300

0.667

0.00058

Table7:ThisshowsthesamereactionwhentheferrateandDZTAstartedat16degreesCelsius.Asthereactiontakesplace,absorbanceandconcentrationchangewithtime.

Figure7:Thisshowstherelationshipbetweenthetimeandtheconcentrationwhenthereactionstartedat16degreesCelsius.

Temperature(oC)

Rate(R2)

1

0.796

4

0.797

8

0.265

12

0.681

16

0.913

Table8:Thisshowsthefinalreactionratestakenfromtheequationsinthepreviousfigures.

Figure8:Thisgraphshowsthefinalrelationshipsbetweentherateofreactionandinitialtemperatureofthesolution.

Discussion:

Thehypothesissuggestedanevolutionofthetimethereactionwouldtakeinfunctionofadecreasingtemperature.

Toachievethedecreaseofthetemperatureforthesolution,asmallplasticbowlwasfilledwithcrushedice.Eachtime,thedilutedferratesolutionandtheDTZAwereproppedintheicebowlandcooledtothedesiredtemperatures(e.g16,12,8,4,1degreesCelsius)

TheSpectraVisspectrometerwascalibratedonfullspectrummodewithacuvettefilledwithDIwater.Theferratesolutionproducedinpart1ofthemainexperimentwasthenputinthespectrometerandameasureoftheabsorbanceat510nmwasdoneandwasshowntobesuperiorto1.5.Thesolutionwasthendilutedandstoredforallfuturetests.

ThedilutedferratesolutionandtheDTZAwerethenmixedandputinthespectrometerwheretheabsorbancevalueswererecordedevery30secondsduring5minutes.Thecuvettewasthencleanedandtheprocessredonewithanothertemperatureuntilallthetemperatureslistedearlierwasrecorded.

Thisconcludedtheexperimentthatwassupposedtotestourhypothesis.

LimitationandImprovement:

Butr

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