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Lactometer Use in Milk Quality Testing

This document discusses milk testing and quality control. It provides an overview of why quality control is important at various stages of milk production and processing from the farm to marketing. Key points covered include: - Quality control ensures milk and milk products meet standards for composition, purity and microorganism levels. It is important for producers, processors, consumers and public health. - Common techniques for quality control testing discussed are milk sampling, preservation of samples, labeling, and basic tests like organoleptic and clot on boiling. - Quality control is important at the farm, milk collection centers, dairy factories during processing and marketing of products. Maintaining quality ensures fair prices and protects public health.

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Ranjan Pal
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100% found this document useful (2 votes)
2K views11 pages

Lactometer Use in Milk Quality Testing

This document discusses milk testing and quality control. It provides an overview of why quality control is important at various stages of milk production and processing from the farm to marketing. Key points covered include: - Quality control ensures milk and milk products meet standards for composition, purity and microorganism levels. It is important for producers, processors, consumers and public health. - Common techniques for quality control testing discussed are milk sampling, preservation of samples, labeling, and basic tests like organoleptic and clot on boiling. - Quality control is important at the farm, milk collection centers, dairy factories during processing and marketing of products. Maintaining quality ensures fair prices and protects public health.

Uploaded by

Ranjan Pal
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

8/11/2016

TABLEOFCONTENTSi

BacktoFactsforFarmers

MilktestingandQualityControl

MilkProcessingGuideSeries
Volume2
Publishedby:
FAO/TCP/KEN/6611Project
TrainingProgrammeforSmallScaleDairySectorandDairyTrainingInstituteNaivasha
TABLEOFCONTENTS
[Link]*
[Link]*
2.1WHATISMILKQUALITYCONTROL?*
2.2WHYHAVEMILKQUALITYCONTROL?*
2.3QUALITYCONTROLINTHEMILKMARKETINGCHAININKENYA*
2.4TECHNIQUESUSEDINMILKTESTINGANDQUALITYCONTROL*
2.4.1Milksampling*
2.4.2Samplingmilkforbacteriologicaltesting*
2.4.3Preservationofsample*
[Link]*
2.4.5Commontestingofmilk.*
[Link]*
[Link]

Milktestingandqualitycontrolisanessentialcomponentofanymilkprocessingindustrywhethersmall,
mediumorlargescale.Milkbeingmadeupof87%waterispronetoadulterationbyunscrupulousmiddlemen
[Link],itshighnutritivevaluemakesitanidealmediumfortherapid
multiplicationofbacteria,[Link]
knowthat,inorderforanyprocessortomakegooddairyproducts,goodqualityrawmaterialsareessential.A
milkprocessororhandlerwillonlybeassuredofthequalityofrawmilkifcertainbasicqualitytestsarecarried
outatvariousstagesoftransportationofmilkfromtheproducertotheprocessorandfinallytotheconsumer.
[Link]
easilyavailabletotheemergingsmallscaletomediumscaleprocessorsinKenya.
[Link]

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Forthesereasons,theTrainingProgrammefortheSmallScaleDairySectorunderproject
GOK/FAO/TCP/KEN/6611,hasassembledthisguideonMilkTestingandQualityControlsothatitmaybeused
[Link]
[Link]
plantswithbiggerlaboratoriesmoretestsaretobefoundinthebibliographyattheendofthisbooklet.
[Link]
2.1WHATISMILKQUALITYCONTROL?
Milkqualitycontrolistheuseofapprovedteststoensuretheapplicationofapprovedpractices,standardsand
[Link]
acceptedstandardsforCHEMICALCOMPOSITIONANDPURITYASWELLASLEVELSOFDIFFERENT
MICROORGANISMS.
2.2WHYHAVEMILKQUALITYCONTROL?
TestingmilkandmilkproductsforqualityandmonitoringthatMILKPRODUCTS,PROCESSORSand
[Link]
whywehavetohaveaqualitycontrolsystemforthedairyindustryinKenya.
Thereasonsare:
i)TotheMilkProducer.
Themilkproducerexpectsafairpriceinaccordancewiththequalityofmilkshe/heproduces.
ii)TheMilkProcessor.
Themilkprocessorwhopaystheproducermustassurehimself/herselfthatthemilkreceivedforprocessingis
ofnormalcompositionandissuitableforprocessingintovariousdairyproducts.
iii)TheConsumer.
Theconsumerexpectstopayafairpriceformilkandmilkproductsofacceptabletoexcellentquality.
iv)ThePublicandGovernmentAgencies.
Thesehavetoensurethatthehealthandnutritionalstatusofthepeopleisprotectedfromconsumptionof
contaminatedandsubstandardfoodstuffsandthatpricespaidarefairtothemilkproducers,themilkprocessor
andthefinalconsumer.
Alltheaboveisonlypossiblethroughinstitutionofaworkablequalitytestingandassurancesystemconforms
tonationalorinternationallyacceptablestandards.
2.3QUALITYCONTROLINTHEMILKMARKETINGCHAININKENYA
i)Atthefarm
[Link]
practicesofmilkproductionandhandlingandobservationoflaiddownregulationsregarding,useofveterinary
drugsonlactatinganimals,regulationsagainstadulterationsofmilketc.
ii)AtMilkcollectionCentres
Allmilkfromdifferentfarmersorbulkedmilkfromvariouscollectingcentresmustbecheckedfor
wholesomeness,bacteriological,andchemicalquality.
iii)AttheDairyFactories
Milkfromindividualfarmersorbulkedmilkfromvariouscollectingcentres
iv)WithintheDairyFactory
Oncethedairyfactorhasacceptedthefarmermilkithastheresponsibilityofensuringthatthemilkishandled
[Link]
conformtospecifiedstandardsastotheadequacyofeffectofprocessesappliedandthekeepingqualityof
[Link]

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[Link]
[Link].
v)Duringmarketingofprocessedproducts
PublicHealthauthoritiesareemployedbylawtocheckthequalityoffoodstuffssoldforpublicconsumption
[Link]
doneinordertoprotecttheinterestofthemilkconsumingpublic.
2.4TECHNIQUESUSEDINMILKTESTINGANDQUALITYCONTROL
2.4.1Milksampling
[Link]
tanksshouldbethoroughlymixedtodispersethemilkfatbeforeamilksampleistakenforanychemicalcontrol
[Link]
dippersmeusedinsamplingmilkfrommilkcans.
2.4.2Samplingmilkforbacteriologicaltesting
[Link]
autoclaveorpressurecookerforatleast15mmat120Cbeforehandinordernottocontaminatethesample.
Onthespotsterilisationmaybeemployedusing70%Alcoholswabandflamingorscalinginhotsteamor
boilingwaterfor1minute.

Fig.1:Equipmentusedfortakingmilksamples
2.4.3Preservationofsample
Milksamplesforchemicaltests.
MilksamplesforbutterfattestingmaybepreservedwithchemicalslikePotassiumdichromate(1Tabletorml
14%solutioninalitresamplebottleisadequate.)Milksamplesthathavebeenkeptcoolingarefrigeratoror
iceboxmustfirstbewarmedinwaterbathat40C,cooledto20C,mixedandasamplethentakenfor
butterfatdetermination.OtherpreservativechemicalsincludeSodiumazidattherateof0.08%andBronopol(2
bromo2nitro1,3propanediol)usedattherateof0.02%.
Ifthelaboratorycannotstartworkonasampleimmediatelyaftersampling,thesamplemustbecooledtonear
[Link]
milkcoolingcentre,iceboxeswithicepecksareuseful.
[Link]
Samplesmustbeclearlylabelledwithnameoffarmerorcodenumberandrecordsofdates,andplaces
[Link]
producersshouldseetheirmilkbeingtested,andtherecordsshouldbemadeavailabletothemiftheyso
require.
2.4.5Commontestingofmilk.
2.4.5.1Organoleptictests
[Link]
isrequired,butthemilkgradermusthavegoodsenseofsight,[Link]
obtainedinstantly,[Link]
mustbesubjectedtoothermoresensitiveandobjectivetests.
Procedure:
[Link]

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Openacanofmilk.
Immediatelysmellthemilk.
Observetheappearanceofthemilk.
Ifstillunabletomakeaclearjudgement,tastethemilk,[Link]
bucketprovidedforthatpurposeorintoadrainbasin,flushwithwater.
Lookatthecanlidandthemilkcantocheckcleanliness.
Judgement:
Abnormalsmellandtastemaybecausedby:
Atmospherictaint([Link]/cowyodour).
Physiologicaltaints(hormonalimbalance,cowsinlatelactationspontaneousrancidity).
Bacterialtaints.
Chemicaltaintsordiscolouring.
Advancedacidification(pH<6.4).
2.4.5.2ClotonBoiling(C.O.B)Test
[Link](pH<5.8)orabnormalmilk([Link]
ormastitismilk).Ifamilksamplefailsinthetest,themilkmustcontainmanyacidorrennetproducing
[Link]
standtheheattreatmentinmilkprocessingandmustthereforeberejected.
Procedure:
Boilasmallamountofmilkinaspoon,[Link],coagulationor
precipitation,[Link],when
theacidityisbelow0.200.26%Lacticacid.

[Link]
[Link].TheAlcoholTest
[Link]/orrennetare
[Link](colostrummilk)andsalt
concentrates(mastitis)resultsinapositivetest.
Procedure:
Thetestisdonebymixingequalamountsofmilkand68%ofethanolsolutioninasmallbottleortesttube.(68
%Ethanolsolutionispreparedfrom68mls96%(absolute)alcoholand28mlsdistilledwater).Ifthetestedmilk
isofgoodquality,therewillbenocoagulation,clottingorprecipitation,butitisnecessarytolookforsmall
lumps.Thefirstclottingduetoaciddevelopmentcanfirstbeseenat0.210.23%[Link]
2mlsmilkismixedwith2mls68%alcohol.

[Link]
[Link]

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[Link].TheAlcoholAlizarintest
[Link]
[Link]
madeorbepreparedbyadding0.4grammesalizarinpowderto1litreof61%alcoholsolution.
RESULTSOFTHETEST
Parameter

Normalmilk

SlightlyacidMilk

Acidmilk

AlkalineMilk

PH

6.66.7

6.46.6

6.3orlower

6.8orhigher

Colour

Redbrown

Yellowishbrown

Yellowish

Lilac

Appearanceof
milk

Nocoagulationno
lumps

Nocoagulation

Coagulation*

Nocoagulation**

Note:
*=Sourmilklooksyellowishwithsmalllumpsorcompletelycoagulated.
**=[Link],indicatemastitismilk.
2.4.5.5Aciditytest
[Link]
[Link],thepercentageof
[Link]"naturalacidity"whichisduetothenatural
abilitytoresistpHchanges.Thenaturalacidityofmilkis0.160.18%.Figureshigherthanthissignifies
developedacidityduetotheactionofbacteriaonmilksugar.
Apparatus:
Aporcelaindishorsmallconicalflask
10mlpipette,graduated
1mlpipette
ABurette,0.1mlgraduations
Aglassrodforstirringthemilkinthedish
APhenophtaleinindicatorsolution,0.5%in50%Alcohol
NSodiumhydroxidesolution.

[Link]
Procedure:
9mlofthemilkmeasuredintotheporcelaindish/conicalflask,1mlPhenopthaleinisaddedandthenslowly
fromtheburret,0.1NSodiumhydroxideundercontinuousmixing,untilafaintpinkcolourappears.
ThenumberofmlsofSodiumhydroxidesolutiondividedby10expressesthepercentageoflacticacid.
2.4.5.6Resazurintest.
[Link]
[Link]
[Link]

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solutioncanlaterbeusedtotestthemicrobialactivityinagivenmilksample.
Resazurincanbecarriedoutas:

i.10mintest.
ii. 1hrtest.
iii.3hrtest.
The10minResazurintestisusefulandrapid,screeningtestusedatthemilkplatform.
The1hrtestand3hrtestsprovidemoreaccurateinformationaboutthemilkquality,butafterafairylongtime.
Theyareusuallycarriedoutinthelaboratory.
Apparatusandreagents:
Resazurintablets
Testtubeswith10mlsmark
1mlpipetteordispenserforResazurinsolution.
Waterbaththermostaticallycontrolled
LovibondcomparatorwithResazurindisc4/9

[Link]
Procedure:
[Link]
solutionmustnotbeexposedtosunlight,anditshouldnotbeusedformorethaneighthoursbecauseitlosses
strength.
Mixthemilkandwithasanitizeddipperput10mlsmilkintoasteriletesttube.
AddonemlofResazurinsolution,stopperwithasterilestopper,mixgentlythedyeintothemilkandmarkthe
tubebeforetheincubationinawaterbath,placethetesttubeinaLovibondcomparatorwithResazurindiskand
compareitcolourimetricallywithatesttubecontaining10mlmilkofthesamesample,butwithoutthedye
(Blank).
READINGSANDRESULTS(10MINUTERESAZURINTEST)
ResazurindiscNo.

Colour

Gradeofmilk

Action

Blue

Excellent

Accept

Lightblue

[Link]

Accept

Purple

Good

Accept

Purplepink

Fair

Separate

Lightpink

Poor

Separate

Pink

Bad

Reject

white

Verybad

Reject

2.4.5.7TheGerberButterfattest
Thefatcontentofmilkandcreamisthemostimportantsinglefactorindeterminingthepricetobepaidformilk
suppliedbyfarmersinmanycountries.

[Link]

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Also,inordertocalculatethecorrectamountoffeedrationforhighyieldingdairycows,itisimportanttoknow
[Link]
inthemilkofindividualanimalsmustbeknowninmanybreedingprogrammes.
Butterfattestsarealsodoneonmilkandmilkproductsinordertomakeaccurateadjustmentsofthebutterfat
percentageinstandardisedmilkandmilkproducts.

[Link]
ApparatusforDFtest:
Gerberbutyrameters,06%or08%BF
Rubberstoppersforbutyrometers
10.94or11mlpipettesformilk
10mlspippetesordispensersforGerberAcid
1mlspippetesordispensersforAmylalcohol
standsforbutyrometers
GerberwaterbathReagents:
Gerbersulphuricacid,(1.82g/cc)
Amylalcohol
Treatmentofsamples.
[Link]
40C,mixedgentlyandcooledto20Cbeforethetesting.
Procedure:
[Link]
theneckofthebutyrometer.
Nextadd1mlofAmylalcohol,insertstopperandshakethebutyrometercarefullyuntilthecurddissolvesand
nowhiteparticlescanbeseen.Placethebutyrometerinthewaterbathat65Candkeepitthereuntilasetis
[Link](scale)pointingtowards
thecentreofthecentrifuge.
Spinfor5min.atll00rpm.
Removethebutyrometersfromthecentrifuge.
[Link].
(Note:Whentransferringthebutyrometersfromthecentrifugeintothewaterbathmakesurethatthe
butyrometersareallthetimeheldwiththeNECKPOINTINGUP).
Thefatcolumnshouldbereadfromthelowestpointofthemeniscusoftheinterfaceoftheacidfattothe0
markofthescaleandreadthebutterfatpercentage.
Thebutyrometersshouldbeemptiedintoaspecialcontainerfortheverycorrosiveliquidofacidmilk,andthe
butyrometersshouldbewashedinwarmwateranddriedbeforethenextuse.
APPEARANCEOFTHETEST
Thecolourofthefatcolumnshouldbestrawyellow.
[Link]

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Theendsofthefatcolumnshouldbeclearlyandsharplydefined.
Thefatcolumnshouldbefreefromspecksandsediment.
Thewaterjustbelowthefatcolumnshouldbeperfectlyclear.
Thefatshouldbewithinthegraduation.
PROBLEMSINTESTRESULTS
Curdytests:
Toolightlycolouredorcurdyfatcolumncanbedueto:
Temperatureatmilkoracidorbothtoolow.
Acidtooweak.
Insufficientacid.
Milkandacidnotmixedthoroughly.
Charredtests:
Darkenedfatcolumncontainingblackspeckatthebaseisdueto:
Temperatureofmilkacidmixturetoohigh.
Acidtoostrong.
Milkandacidmixedtooslowly.
Toomuchacidused.
Aciddroppedthroughthemilk.
2.4.5.8TheLactometertest
Additionofwatertomilkcanbeabigproblemwherewehaveunfaithfulfarmworkers,milktransportersand
[Link]
thereforeassurehimself/herselfthatthemilkhe/shepurchasesiswholesomeandhasnotbeenadulterated.
[Link]
committed,[Link]
[Link],it
enablesthemilkprocessortocalculatethemilktotalsolids(%TS)andsolidsnotfat(SNF).Innormalmilk
SNFshouldnotbebelow8.5%accordingtoKenyaStandards(KBSNo05l0:1976).
Procedure:
Mixthemilksamplegentlyandpouritgentlyintoameasuringcylinder(300500).LettheLactometersink
[Link](L)[Link]
temperatureofthemilkisdifferentfromthecalibrationtemperature(Calibrationtemperaturemaybe=200C)of
thelactometer,calculatethetemperaturecorrection.ForeachCabovethecalibrationtemperatureadd0.2L
foreachCbelowcalibrationtemperaturesubtract0.2Lfromtherecordedlactometerreading.
EXAMPLE:Calibrationtemperatureoflactometer20C.

[Link]
Sample

Milktemperature

Lactometer
reading

Correction

Truereading

No.1

17C

30.6L

0.6L

30.0L

No.2

20C

30.0L

Nil

30.0L

[Link]

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No.3

23C

29.4L

+0.6L

30.0L

Forthecalculations,uselactometerdegrees,andfortheconversiontodensitywrite1.0infrontofthetrue
lactometerreading,i.e.1.030g/[Link]
[Link]
[Link]
cowsoftenhavelactometerreadingoutsidetherangeofaveragemilk,whilesamplesofmilkfromherdsshould
havereadingsheartheaveragemilk,butwrongfeeding,[Link]
milktohavespecificgravityof1.0261.032g/[Link]
thereadingisconsistentlylowerthanexpectedandthemilksupplierdisputesanywrongdoingarrangetotakea
genuinesamplefromthesupplier([Link]).
2.4.5.9FreezingPointDetermination
[Link]
adulterationofmilkwithwaterwillcauseadetectableelevationofthefreezingpointofmilkfromitsnormal
[Link],itisusedtodetectwhether
milkisofnormalcompositionandadulterated.

[Link].
2.4.5.10Inhibitortest.
Milkcollectedfromproducersmaycontaindrugsand/[Link]
amountsinmilkmayinhibitthegrowthoflacticacidbacteriausedinthemanufactureoffermentedmilksuchas
Mala,cheeseandYoghurt,besidesbeingahealthhazard.
Principleofthemethod:Thesuspectedmilksampleissubjectedtoafermentationtestwithstartercultureand
theaciditycheckedafterthree(3)[Link]
acidityofasimilarlytreatedsamplewhichisfreefromanyinhibitorysubstances.
Materials:
testtubes
Starterculture
lmlpipette
waterbath
materialfordeterminationoftitratableacidity(Fig.9)

[Link]
Procedure:
Threetesttubesarefilledwithl0mlofsampletobetestedandthreetesttubesfilledwithnormalmilk.
Alltubesareheatedto900Cbyputtingtheminboilingwaterfor35minutes.
[Link]

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Aftercoolingtooptimumtemperatureofthestarterculture(30,37,or42C),1mlofstartercultureisaddedto
eachtesttube,mixedandincubatedfor3hours.
Aftereachhour,onetesttubeisfromthetestsampleandthecontrolsampleisdetermined.
Assessmentofresults:
Ifacidproductioninsuspectedsampleisthesameasthenormalsample,thenthesuspectsampledoesnot
containanyinhibitorysubstances
Ifacidproductionassuspectsampleislessthaninthenormalmilksample,then,thesuspectsamplecontains
antibioticsorotherinhibitorysubstances.
[Link]
Whenmilkispasteurisedat63Cfor30mininbatchpasteuriseror72Cfor15secondsinheatexchanger,
continuousflowpasteurisers,ALLPATHOGENICBACTERIAAREDESTROYED,therebyrenderingmilksafe
[Link],andwhichmightaffectitsflavour,
aredestroyed.
Inordertodeterminewhetherornotmilkhasbeenadequatelypasteurised,oneoftheenzymesnormally
presentinmilkphosphatase,[Link]
[Link],itmeansthepasteurisation
processwasinadequateandthemilkmaynotbesafeforhumanconsumptionandwillhaveashortshelflife.
Testtubes
5mlspipettes
1mlpipettes
l00mlvolumetricflask
500mlvolumetricflask
waterbathat37C
Note:Allglasswaremustberinsed,cleaned,rinsedinchromicacidsolutionandboiledinwaterfor30min.
Reagent:
Buffersolution:
Ismixedby0.75ganhydroussodiumcarbonateandl.75gSodiumbicarbonatein500mldistilledwater.
Buffersubstratesolution:
Place0.l5gofdisodiumparanitrophenylphosphate(thesubstrate)intoaclean100mlmeasuringcylinder.
Addthebuffersolutiontomaketo100mlmark.
[Link]
[Link].
Procedure:
Pipette5mlsbuffersubstratesolutionintoatesttube,stopperandwarmthesolutioninthewaterbathat37C.
Addtothetesttube1mlofthemilktobetested,[Link]
[Link]
[Link],removethetubesandmixthemthoroughly.
PlaceonesampleagainsttheblankinaLovibondcomparator"ALLPURPOSES"[Link]
rotatethediscuntilthecolourofthetestsampleismatchedandreadthediscnumber.
Interpretation:
DiscReadingafter2hrsincubationat37C

Remarks

010

Properlypasteurised

1018

Slightlyunderpasteurised

[Link]

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1842

UNDERPASTEURISED

>42

NOTPASTEURISED

REFERENCES:
ILCAManualNo.4,[Link].
[Link].9002,[Link],
Brussels,Belgium.
Marshall,[Link]
HealthAssociation.

[Link]

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For these reasons, 
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manufactured produc
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Open a can of milk.
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29.4 ºL
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After cooling to o

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