sni 01-0003-1987

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    SNI INDONESIAN NATIONAL STANDARDsNI 01 - 0003 - 1987uDC. 665 - 353 - 4

    PALM KERNEL OIL

    INDONESIAN STANDARDIZATION COUNCIL

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    t.2.3.4.-5.

    CONTENTS

    ScopeDescription ..............Classification ..........

    I

    Quality Requirements .........Sampling5.1. In Drums5.2. In BulkMethods of Test6.1 Determination Free Fatty Acid........6.2 Determination of Impurities content6.3 Determination of Moisture contentLabellingPacking

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    III222J

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    sNr 01 - 0003 - 1987

    PALM KERNEL OIL

    I. SCOPEThis standard specifles the description, classiflcation, quality requirements,rnethods of sarnpling, rnethods of test, label requirements and methods clfpacking tor Perlnr Kernel Oil.2. DESCRIPTION

    Palm Kernel Oii shall be the white-yellowish oil obtained by extraction fromthe fruit kernel of Elaeis guineensis Jacq.3. CLASSIFICATION

    Palrr-r Kernel Oil shall be classified into one grade.4. QUALITY REQUIREMENTS

    TabelQuality Requirements Specification

    No Type of test unit Requirementsl

    2.)

    Free Fatty Acid (as lauric acid),(weight/weight)I rnpurities content (weight/weight)Moistr-rre content (weight/weight)

    7o

    7oo/o

    max.5.0max. 0.05max. 0.45

    5. SAMPLING5.1. In Drums

    The sample shall be taken at random from the square root of the number ofdrums in a consignment with a maximum of 30 drums per consignment. Thesample shall be taken lrom each drum with sampling tube with valve of 125cm in length and a diameter of + 2 cm.

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    sNr 01 - 0003 - 1987

    The orifice of the pipe can be closed or opened by a long stemmed plug. Byimmersing this pipe into the drum, the oil shall be sampled from the upper layerclown to the bortom layer. Samples shall be taken at four cliagonally tppo.itecorners and the four samples are then mixed together and from this mixture Ikg shall be taken fbr analysis.5.2. In Bulk

    Tl-re sarnple shall be taken as a systematic sampling using the specificeqr'ripments as much as I kg of sample from the outflow tap of the pipe throughwhich the oil flows from the land tank to the ship.The sampling oificial shall be a person with experience or training andernployecl by i,r leg;il body.

    6. METHODS OF TEST6.1 Determination of Free Fatty Acid6.t.I Principle

    Dissolution of a test portion in a rnixed solvent, foilowed by titration of thel'r'ee f.atty acicls present with ethanolic soh,rtion o1'potassiurn hydroxide.6.1.2 Reagents6.1 .2.1 Ethan ol 95o/o (v/v)6.1.2.2 NaOH 0.I N, Stiindard volumetric solution6.1-2.3 Phenolphthalein Indicator solution l7o rn957o (vlv) alcohol6. I ..3 Appa.,ttrs6.1.3. I Erlenmeyer flask 250 ml6.1.3.2 Water Bath6. 1.3.3 Buretre6. 1.3.4 Measuring glass

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    6.1.46.t.4.1(t.1.4.2

    6.1.4.3

    6.2.26.2.2.16.2.2.2

    sf{t 01 - 1987

    Test Procedureweigh to the nearest 10 mg about 2 - 50 g of the sample into a flaskHeat to boiling 50 ml of the ethanol in a second flask. while thetempelature of the ethanol is still 70 C neutralize with the KOH 0. I Nsolution, using 0.5 ml of phenolphthaleinAdd the solution tiom the second flask into the test portion in the firstflask and heat to the boiling point and titrate to the end point with the KOH0. lN solution.6.1.5 Expression of results

    Express the results as a percentage by mass of lauric acid using the formula:2.00 T NLauric acid =

    Where :T is the volume (mi) of NaOH used for the titration.N is the normality of NaOHW is the mass (g) of the sample.

    6.2 Determination of Impurities Content6.2.1 Principle

    Treatment of a test portion with an excess of n-hexane or light petroleum,then flltration of the solution obtained. Washing of the filter and residue with

    w

    the same solvent, drying at 103 +2oC. and weighing.Reagents

    Petroleum ether orless than 1 n-Hexane. boiling range 400C to 600C,bromine valueCarbon disulphide, fieshly distilled before use

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    6.2.36.2.3.16.2.3 .2(t.2.3.36.?.3.46.2.3.56.2.16.2.4.16.2.1.26.2.4.36.2.4.4

    sNI 01 - 0003 - 1987Apparatus

    Analytical BalanceF'ilter paper Whatman No. 41Gooch crucible and fiber glass, silica crucibleOvenContinues extraction apparatus

    Test Procedureweigh about 5 g of sarnple to the-nearest 0.1 g into a flask.Melt the test portion, add 250 ml of petroleum ether, close the flash withthe ground glass stopper and shake. Ailow to stand overnight.Decant the solution carefully through an ashless filter paper and dry inthe oven at a temperature of 103 + 2 C.Remove trom the oven, close the vessel with its lid, allow to cool in thedesiccator and weigh to the nearest 0.001 g.

    PrincipleHeating a test portion at 103t2'C and cletermining the loss in mass

    6.2.5 Expression of resr.rltsThe organic impr,rrities content expressed as a percentage by mass, nsing thelbrmula :

    100(M, _ Mr) XWhere :

    M,,M,, is the mass (g) of the rest portionMr is the mass (g) of the vessel with its lid and filter paper or ofthe filter crucibleM, is the mass (g) of the vessel with its lid and filter pelper,containing the dry residue or of the fllter crucible and dryresidue.

    6.3 f)etermination of Moisture Content6.3. I

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    6.3.2(t.3 .2.l6.3.2.26.3.2.3

    6.3.36.3.3.16.3.3.26.3 3.36.3.3.4

    6.3.3.5

    sNr 01 - 0003 - 1987

    ApparatusMetal dish, flatbottomedwith a diameterof 80 rnmto 90 mmanda depthof 40 mm to 50 mmOven, capable of being maintained at temperature of I 03 + 2 CDesicator, containing an efficient desiccant such as phosphorus pentox-ide, silica gel or activated alumina.

    Test ProcedureWeigh in a tared dish about 10 g of sample to the nearest l0 mg.Heat the dish containing the test portion for t hour in the oven, maintainedat a temperature of 103 + 2 C.Remove the dish, allow it to cool in the desiccator and weigh.Repeat the heating and weighing of the test portion under the samecondition r-rntil the difference in mass between two succesive weighingdoes not exceed 2 ^9.Record the mass of the portion and residue on the work sheet

    6.3.4 Expression of resultsThe result shall be expressed as a percentage by mass, using the formula :

    (Mo - Mr)100

    MrWhere:M,, is the mass of theMr is the mass of the test portion (g)residue (g)

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    7. LABELLINGFor each shipment. on the outer surf-ace of each clrum withshall be written :

    sNI 01 - 0003 _ 1981

    non f-ading paint

    8. PACKINGPalm Kernel oil shall be presented as a liquid, in bulk or packed in a clean anddry drLrm, with a capacity of 200 litres wlth a head space of 5 - I0 percent.Drums for Palm Kernel oil should be made of a material iron sheet plate withtin or galvanized iron sheets or iron sheet coated on the inside with a layerwhich does not aff-ect the palm Kernel Oil.

    Produce in InclonesiaName of company/ExporterName of commodityCode ol'ProdLrctionNet weighrCountry of destinationOther important deciarations

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