Regulations, 2005

L.N. 141 of 2005

VETERINARY SERVICES ACT, 2001

(ACT NO. XXIII OF 2001)

Methods of Analysis for the Official Control of Feeding-Stuffs

Regulations, 2005

IN exercise of the powers conferred by article 22(c) of the

Veterinary Services Act, the Minister for Rural Affairs and the

Environment, after consultation with the Minister of Health, the Elderly

and Community Care, has made the following rules>-

(1) The title to these regulations is the Methods of Analysis

for the Official Control of Feeding-Stuffs Regulations, 2005.

(2) The scope of these regulations is to implement the

provisions found under European Union Council Directive 71#250#EEC

on the methods of analysis for the official control of feeding-stuffs.

For the purpose of these regulations -

METHODS OF ANALYSIS OF THE COMPONENTS OF FEEDING STUFFS

1. GENERAL PROVISIONS ON METHODS OF ANALYSIS FOR FEEDINGSTUFFS

A. PREPARATION OF SAMPLES FOR ANALYSIS

1. PURPOSE

The procedures described below concern the preparation for analysis of final samples, sent to the control

laboratories after sampling in accordance with the provisions laid down by First Commission Directive

76/371/EEC of 1 March 1976 establishing Community methods of sampling for the official control of

feeding stuffs.

These samples must be prepared in such a way that the amounts weighed out, as provided for in the

methods of analysis, are homogeneous and representative of the final samples.

2. PRECAUTIONS TO BE TAKEN

All the necessary operations must be performed in such a way as to avoid as far as possible contamination

of the sample and changes of its composition. Grinding, mixing and sieving should be carried out as

quickly as possible with minimal exposure of the sample to the air and light. Mills and grinders likely to

appreciably heat the sample should not be used. Manual grinding is recommended for feedingstuffs which

are particularly sensitive to heat. Care should also be taken to ensure that the apparatus itself is not a source

of contamination of trace elements.

If the preparation cannot be carried out without significant changes in the moisture content of the sample,

determine the moisture content before and after preparation according to the method laid down in Part 1 of

the Annex to Second Commission Directive 71/393/EEC of 18 November 1971 establishing Community

methods of analysis for the official control of feedingstuffs, as amended by Commission Directive

73/47/EEC of 5 December 1972.

3. PROCEDURE

Mix thoroughly the final sample either mechanically or manually. Divide the sample into two equal

portions (the quartering method should be used where applicable). Keep one of the portions in a suitable

clean, dry container, fitted with an air-tight stopper, and prepare the other portion or a representative part of

it, of at least 100 g, as indicated below.

3.1. Feeding stuffs which can be ground as such

Unless otherwise specified in the methods of analysis, sieve the whole sample through a sieve

with a square mesh of 1 mm side (in accordance with recommendation ISO R565) after grinding,

if necessary. Avoid any overgrinding.

Mix the sieved sample and collect it in a suitable clean, dry container fitted with an air-tight

stopper. Mix again, immediately before weighing out the amount for analysis.

3.2. Feeding Stuffs which can be ground after drying

Unless otherwise specified in the methods of analysis, dry the sample to bring its moisture

content down to a level of 8 to 12 %, according to the preliminary drying procedure described

under point 4.3 of the method of determination of moisture mentioned in section 2 above. Then

proceed as indicated in section 3.1.

3.3. Liquid or semi-liquid feeding stuffs

Collect the sample in a suitable clean, dry container, fitted with an air-tight stopper. Mix

thoroughly immediately before weighing out the amount for analysis.

3.4. Other feeding stuffs

Samples which cannot be prepared according to one of the above procedures should be treated

by any other procedure which ensures that the amounts weighed out for the analysis are

homogeneous and representative of the final samples.

“Act” means the Veterinary Services Act, 2001<

“the Community” means the European Community as

established under the Treaty establishing the European Community<

“the Commission” means the European Commission<

“Competent Authority” means the Veterinary Services within

the territory of Malta as provided under article 2 of the Veterinary

Services Act<

“Member State” means a State which is a Member within the

European Community.

(1) The Competent Authority shall require that analyses for

official controls of feeding-stuffs within its jurisdiction as regards their

levels of hydrocyanic acid, calcium, carbonates, crude ash, ash insoluble

in HCl chlorine from chlorides, lactose, potassium, sodium, sugars and

urea, and the estimation of the urease activity of products derived from

soya be carried out using the methods set out in the Schedule to these

regulations.

(2) The general rules contained in Part 1 of the Schedule

shall apply to the methods of analysis adopted pursuant to Council

Directive 70#373#EEC.

(3) As regards undesirable substances within the meaning

of Directive 2002#32#EC of the European Parliament and of the Council

including dioxins and dioxin-like PCBs, point C(3) of Part 1 of the

Annex to this Directive shall apply.

Storage of samples

Samples must be stored at a temperature that will not alter their composition. Samples intended for the

analysis of vitamins or substances which are particularly sensitive to light should be stored in brown

glass containers.

B. PROVISIONS RELATING TO REAGENTS AND APPARATUS USED IN METHODS OF

ANALYSIS

1. Unless otherwise specified in the methods of analysis, all analytical reagents must be analytically pure

(a.p.). When determining trace elements, the purity of the reagents must be checked by a blank test.

Depending upon the results obtained, further purification of the reagents may be required.

2. Any operation involving preparation of solutions, dilution, rinsing or washing, mentioned in the

methods of analysis without indication as to the nature of the solvent or diluent employed, implies that

water must be used. As a general rule, water should be demineralized or distilled. In particular cases,

which are indicated in the methods of analysis, it must be submitted to special procedures of

purification.

3. In view of the equipment normally found in control laboratories, only those instruments and apparatus

which are special or require specific usage are referred to in the methods of analysis. They must be

clean, especially when very small amounts of substances have to be determined.

C. APPLICATION OF METHODS OF ANALYSIS AND EXPRESSION OF THE RESULTS

1. In general a single method of analysis is established for the determination of each substance in

feedingstuffs. Where several methods are given, the particular method used by the control laboratory

must be indicated on the analysis report.

2. The result given in the analysis report shall be the average value obtained from at least two

determinations, carried out on separate portions of the sample, and of satisfactory repeatability.

This result shall be expressed in the manner laid down in the method of analysis to an appropriate

number of significant figures and shall be corrected, if necessary, to the moisture content of the final

sample prior to preparation.

3. As regards undesirable substances within the meaning of Directive 2002/32/EC, including dioxins and

dioxin-like PCBs, a product intended for animal feed shall be considered as non compliant with the

established maximum content, if the analytical result is deemed to exceed the maximum content taking

into account expanded measurement uncertainty and correction for recovery. The analysed

concentration corrected for recovery and the expanded measurement uncertainty subtracted from the

analytical result is used to assess compliance. This procedure is only applicable in cases where the

method of analysis enables the estimation of measurement uncertainty and correction for recovery (eg.

Not possible in case of microscopic analysis)

The analytical result shall be reported as follows (in so far the used method of analysis enables to

estimate the measurement uncertainty and recovery rate)

(a) corrected or uncorrected for recovery, the manner of reporting and the level of recovery being

indicated;

(b) as “x +/- U”, whereby x is the analytical result and u is the expanded measurement uncertainty,

using a coverage factor of 2 which gives a level of confidence of approximately 95%.’

2. DETERMINATION OF HYDROCYANIC ACID

1. PURPOSE AND SCOPE

This method makes it possible to determine the level of hydrocyanic acid, free and combined in the

form of glycosides, in feeding-stuffs and in particular in products derived from flax seed, manioc flour

and certain species of beans.

2. PRINCIPLE

The sample is suspended in water. The hydrocyanic acid is released by the action of enzymes,

entrained by steam distillation and collected in a specific volume of acidified silver nitrate solution.

The silver cyanide is separated by filtration and the excess silver nitrate is titrated with a solution of

ammonium thiocyanate.

3. REAGENTS

3.1. A suspension of sweet almonds: crush twenty blanched sweet almonds in 100 ml of water at 37

to 40 ºC. Check that there is no hydrocyanic acid in 10 ml of the suspension using sodium

picrote paper or by carrying out a blank test as described in the last paragraph of 5.

3.2. 10% solution (w/v) of sodium acetate, neutral to phenolphthalein.

3.3. Anti-foaming emulsion (e.g. silicone).

3.4. Nitric acid, d: 1·40.

3.5. Silver nitrate solution: 0·02 N.

3.6. Ammonium thiocyanate solution: 0·02 N.

3.7. Saturated solution of ammonium ferric sulphate.

3.8. Ammonia, d: 0·958.

4. APPARATUS

4.1. Oven with thermostat set at 38 ºC.

4.2. Apparatus for distillation by entrainment in steam fitted with a condenser with a curved

extension piece.

4.3. 1000 ml flat-bottomed flasks with ground-glass stoppers.

4.4. Oil bath.

4.5. Burette graduated in 1/20 ml.

PROCEDURE

Weigh 20 g of the sample to the nearest 5 mg, place in 1 litre flat-bottomed flask and add 50 ml of

water and 10 ml of sweet almond suspension (3.1.). Stopper the flask and transfer to the oven for

sixteen hours at 38 ºC. Next, cool to room temperature and add 80 ml of water, 10 ml of sodium

acetate solution (3.2) and a drop of anti-foaming emulsion (3.3).

Connect the flask to the steam distillation apparatus and place in an oil bath which has first been

brought to a temperature slightly above 100 ºC. Distil 200 to 300 ml of liquid by passing a powerful

current of steam through the flask and gently heating the oil-bath. Collect the distillate in an

Erlenmeyer flask protected from the light and containing exactly 50 ml of silver nitrate solution 0·02 N

(3.5) and 1 ml of nitric acid (3.4). Make sure that the condenser's extension piece is immersed in the

silver nitrate solution.

Transfer the contents of the Erlenmeyer flask to a 500 ml volumetric flask, make up to volume with

water, stir and filter. Remove 250 ml of the filtrate, add approximately 1 ml solution of ammonium

ferric sulphate (3.7) and back-titrate the excess silver nitrate with the solution of ammonium

thiocyanate 0·02 N (3.6) taken from the burette graduated in 1/20 ml.

A blank test may, if required, be carried out by applying the same procedure to 10 ml of sweet almond

suspension (3.1), omitting the sample to be analysed.

CALCULATION OF RESULTS

If the blank test indicates that silver nitrate solution 0.02 N has been consumed, subtract the value of

this from the volume consumed by the distillate of the sample. 1 ml of AgNO 3 0·02 N corresponds to

0·54 mg of HCN. Express the result as a percentage of the sample.

OBSERVATIONS

If the sample contains a large quantity of sulphides (e.g. beans), a black precipitate of silver sulphide is

formed which is filtered together with the silver cyanide deposit. The formation of this precipitate

causes a loss of silver nitrate solution 0·02 N, the volume of which must be subtracted from the

volume used to calculate the HCN content. To do this, proceed as follows

Treat the deposit left on the filter with 50 ml of ammonia (3.8) in order to dissolve the silver cyanide.

Wash the residue in dilute ammonia and then determine its silver content. Convert the value obtained

into ml of silver nitrate solution 0·02 N.

The sample's HCN content may also be determined by titrating the acidified ammoniacal filtrate with

nitric acid.

3. DETERMINATION OF CALCIUM

1. PURPOSE AND SCOPE

The method makes it possible to determine the total calcium content of feeding-stuffs.

2. PRINCIPLE

The calcium is ashed, the ash treated with hydrochloric acid and the calcium precipitated as calcium

oxalate. Dissolve the precipitate in sulphuric acid and titrate the oxalic acid which forms with a

solution of potassium permangante.

3. REAGENTS

3.6. Hydrochloric acid A.R., d: 1·14

3.2. Nitric acid A.R., d: 1·40

3.3. Sulphuric acid A.R., d: 1·13

3.4. Ammonia A.R., d: 0·98

3.5. Cold saturated solution of ammonium oxalate A.R.

3.6. 30% solution (w/v) of citric acid A.R.

3.7. 5% solution (w/v) of ammonium chloride A.R.

3.8. 0·04% solution (w/v) of bromo-cresol green

3.9. Solution of potassium permanganate 0·1 N

4. APPARATUS

4.1. Electric muffle-furnace with air circulation and thermostat.

4.2. Platinum, silica or porcelain crucibles for ashing.

4.3. Glass filter crucibles of G4 porosity.

5. PROCEDURE

Weigh approximately 5 g of the sample (or more if necessary) to the nearest mg, calcine at 550 ºC and

transfer the ash to a 250 ml beaker.

Add 40 ml of hydrochloric acid (3.1), 60 ml of water and a few drops of nitric acid (3.2). Bring to the

boil and keep at boiling point for thirty minutes. Cool and transfer the solution to a 250 ml volumetric

flask. Rinse, bring the volume up to the mark with water, homogenise and filter.

Using a pipette, remove to a 250 ml beaker an aliquot amount containing 10 to 40 mg of calcium

according to the assumed calcium content. Add 1 ml of citric acid solution (3.6) and 5 ml of

ammonium chloride solution (3.7).

Make the volume up to approximately 100 ml with water. Bring to the boil, add eight to ten drops of

bromo-cresol green solution (3.8) and 30 ml of a warm solution of ammonium oxalate (3.5). If a

precipitate forms, dissolve it by adding a few drops of hydrochloric acid (3.1).

Neutralise very slowly with ammonia (3.4), stirring continuously until a pH reading of 4.4 to 4.6 is

obtained (i.e. when the indicator changes colour).

Place the beaker in a boiling water bath and keep there for thirty minutes to allow the precipitate

which has formed to settle. Remove the beaker from the water bath. Leave it to stand for an hour and

filter through a G 4 filter crucible.

Wash the beaker and the crucible with water until the excess ammonium oxalate is completely

removed (the absence of chloride in the washing water indicates that they have been sufficiently

washed).

Dissolve the precipitate on the filter in 50 ml of warm sulphuric acid (3.3). Rinse the crucible with

warm water and make the filtrate up to approximately 100 ml. Bring the temperature up to 70—80 ºC

and titrate drop by drop with a solution of potassium permanganate (3.9) until a pink colour is

obtained which lasts for one minute.

6. CALCULATION OF RESULTS

1 ml of potassium permanganate 0·1 N corresponds to 2·004 mg of calcium. Express the result

obtained as a percentage of the sample.

7. OBSERVATIONS

7.1. For very low contents of calcium proceed as follows: filter the calcium oxalate precipitate

through an ash-free filter paper. After washing, dry the filter and ash at 550 ºC in a platinum

crucible. Redissolve the residue in a few drops of sulphuric acid (3.3), evaporate until dry,

calcine again at 550 ºC and weigh. If W is the weight of the calcium sulphate obtained, the

calcium content of the aliquot amount taken as a sample = W × 0·2944.

7.2. If the sample consists solely of mineral substances, dissolve in hydrochloric acid without ashing

it first. In the case of products such as calcium-aluminium phosphate which are difficult to

dissolve in acid, melt as follows by an alkaline process before dissolving: mix the sample to be

analysed thoroughly in a platinum crucible with a mixture five times its weight, consisting of

equal amounts of potassium carbonate and sodium carbonate. Heat carefully until the mixture is

completely melted. Cool, and dissolve in hydrochloric acid.

7.3. If the magnesium content of the sample is high, precipitate the calcium oxalate a second time.

4. DETERMINATION OF CARBONATES

1. PURPOSE AND SCOPE

This method makes it possible to determine the amount of carbonates, conventionally expressed as

calcium carbonate, in most feeding-stuffs.

However in certain cases (for example, with iron carbonate) a special method must be used.

2. PRINCIPLE

The carbonates are decomposed in hydrochloric acid; the carbon dioxide released is collected in a

graduated tube, and its volume compared with that released under the same conditions by a known

quantity of calcium carbonate A.R.

3. REAGENTS

3.1. Hydrochloric acid, d: 1·10.

3.2. Calcium carbonate, A.R.

3.3. Sulphuric acid, approximately 0·1 N, coloured with methyl red.

4. APPARATUS

Scheibler-Dietrich apparatus (see diagram) or equivalent apparatus.

5. PROCEDURE

According to the sample's carbonate content, weigh a portion of the sample as shown below

0·5 g

for products containing from 50 to 100 % of carbonates, expressed as calcium carbonate;

1 g

for products containing from 40 to 50% of carbonates, expressed as calcium carbonate;

2 to 3 g

for other products.

Place the portion of the sample in the special flask (4) of the apparatus, fitted with a small tube of

unbreakable material containing 10 ml of hydrochloric acid (3.1), and connect the flask to the

apparatus. Turn the three-way cock (5) so that the tube (1) connects with the outside. Using the mobile

tube (2), which is filled with coloured sulphuric acid (3.3) and connected to the graduated tube (1),

bring the level of the liquid up to the zero mark. Turn the cock (5) in order to connect up tubes (1) and

(3) and check that the level is at zero.

Run the hydrochloric acid (3.1) slowly over the portion of the sample, tilting the flask (4). Make the

pressure equal by lowering the tube (2). Shake the flask (4) until the release of carbon dioxide has

stopped completely.

Restore pressure by bringing the liquid back to the same level in tubes (1) and (2). After a few minutes,

when the volume of gas has become constant, take the reading.

Carry out a control test in the same conditions on 0·5 g of calcium carbonate (3.2).

6. CALCULATION OF RESULTS

The content in grammes of carbonates, expressed as calcium carbonate, as a percentage of the sample,

is calculated by using the formula

V x 100

T x 2W

where

V = ml of CO 2 released by the portion of the sample.

T = ml of CO 2 released by 0·5 g of CaCO 3 A.R.

W = weight, in grammes, of the portion of the sample.

7. OBSERVATIONS

7.1. When the portion of the sample weighs more than 2 g, first place 15 ml of distilled water in the

flask (4) and mix before beginning the test. Use the same volume of water for the control test.

7.2. If the apparatus used has a different volume from that of the Scheibler- Dietrich apparatus, the

portions taken from the sample and from the control substance and the calculation of the results

must be adapted accordingly.

5. DETERMINATION OF CRUDE ASH

1. PURPOSE AND SCOPE

This method makes it possible to determine the crude ash content of feedingstuffs.

2. PRINCIPLE

The sample is ashed at 550 ºC; the residue is weighed.

3. REAGENTS

20% solution (w/v) of ammonium nitrate.

4. APPARATUS

4.1. Hot-plate.

4.2. Electric muffle-furnace with thermostat.

4.3. Crucibles for ashing made of platinum or an alloy of platinum and gold (10% Pt, 90 Au), either

rectangular (60 × 40 × 25 mm) or circular (diameter: 60 to 75 mm, height: 20 to 25 mm).

5. PROCEDURE

Weigh out to the nearest mg approximately 5 g of the sample (2·5 in the case of products which have a

tendency to swell) and place in a crucible for ashing which has first been calcined and tared. Place the

crucible on the hot-plate and heat gradually until the substance carbonises. Put the crucible into the

muffle-furnace set at 550 ºC ± 5 ºC. Keep at this temperature until white, light grey or reddish ash is

obtained which appears to be free from carbonaceous particles. Place the crucible in a desiccator, leave

to cool and weigh immediately.

6. CALCULATION OF RESULTS

Calculate the weight of the residue by deducting the tare.

Express the result as a percentage of the sample.

7. OBSERVATIONS

7.1. The ash of substances which are difficult to ash must be subjected to an initial ashing of at least

three hours, cooled and then a few drops of 20% solution of ammonium nitrate added to it

(carefully, to avoid dispersal of the ash or the formation of lumps). Continue calcining after

drying in the oven. Repeat the operation as necessary until ashing is complete.

7.2. In the case of substances resistant to the treatment described under 7.1, proceed as follows: after

ashing for three hours, place the ash in warm water and filter through a small, ash-free filter. Ash

the filter and its contents in the original crucible. Place the filtrate in the cooled crucible,

evaporate until dry, ash and weigh.

7.3. In the case of oils and fats, weigh accurately a sample of approximately 25 g in a suitably sized

crucible. Carbonise by setting light to the substance with a strip of ash-free filter paper. After

combustion, moisten with as little water as possible. Dry and ash as described under 5.

6. DETERMINATION OF ASH WHICH IS INSOLUBLE IN HYDROCHOLORIC ACID

1. PURPOSE AND SCOPE

This method makes it possible to determine the level in feeding-stuffs of mineral substances which are

insoluble in hydrochloric acid. Two methods can be used, depending on the nature of the sample.

1.1. Method A: applicable to straight organic feeding-stuffs and to most compound feeding-stuffs;

1.2. Method B: applicable to mineral compounds and mixtures and to compound feeding-stuffs

whose content in substances insoluble in hydrochloric acid, as determined by Method A, is

greater than 1 %.

2. PRINCIPLE

2.1. Method A: the sample is ashed, the ash boiled in hydrochloric acid and the insoluble residue

filtered and weighed.

2.2. Method B: the sample is treated with hydrochloric acid. The solution is filtered, the residue ashed

and the ash thus obtained treated in accordance with Method A.

3. REAGENTS

3.1. Hydrochloric acid 3 N.

3.2. 20% solution (w/v) of trichloroacetic acid.

3.3. 1% solution (w/v) of trichloroacetic acid.

4. APPARATUS

4.1. Hot plate.

4.2. Electric muffle-furnace with thermostat.

4.3. Crucibles for ashing made of platinum or an alloy of platinum and gold (10% Pt, 90% Au), either

rectangular (60 × 40 × 25 mm) or circular (diameter 60 to 75 mm, height: 20 to 25 mm).

5. PROCEDURE

5.1. Method A

Ash the sample using the method described for the determination of crude ash. Ash obtained

from that analysis may also be used. Place the ash in a 250 to 400 ml beaker using 75 ml of

hydrochloric acid 3 N (3.1). Bring slowly to the boil and boil gently for fifteen minutes. Filter

the warm solution through an ash-free filter paper and wash the residue with warm water until

the acid reaction is no longer visible. Dry the filter containing the residue and ash in a tared

crucible at a temperature of not less than 550 ºC and not more than 700 ºC. Cool in a desiccator

and weigh.

5.2. Method B

Weigh 5 g of the sample to the nearest mg and place in a 250 to 400 ml beaker. Add 25 ml of

water and 25 ml of hydrochloric acid 3 N (3.1) successively, mix and wait for effervescence to

cease. Add a further 50 ml of hydrochloric acid 3 N (3.1). Wait for any release of gas to cease

then place the beaker in a boiling water bath and keep it there for thirty minutes or longer, if

necessary, in order to hydrolyse thoroughly any starch which may be present.

Filter while warm through an ash-free filter and wash the filter in 50 ml of warm water (see

observation 7). Place the filter containing the residue in a crucible for ashing, dry and ash at a

temperature of not less than 550 ºC and not more than 700 ºC. Place the ash in a 250 to 400 ml

beaker using 75 ml of hydrochloric acid 3 N (3.1); continue as described in the second

subparagraph of 5.1.

6. CALCULATION OF RESULTS

Calculate the weight of the residue by deducting the tare. Express the result as a percentage of the

sample.

7. OBSERVATION

If filtration proves difficult recommence the analysis, replacing the 50 ml of hydrochloric acid 3 N

(3.1) by 50 ml of 20% trichloroacetic acid (3.2) and washing the filter in a warm solution of 1%

trichloroacetic acid (3.3).

7. DETERMINATION OF CHLORINE FROM CHLORIDES

1. PURPOSE AND SCOPE

This method makes it possible to determine the amount of chlorine in chlorides which are soluble in

water, conventionally expressed as sodium chloride. It is applicable to all feeding-stuffs.

2. PRINCIPLE

The chlorides are dissolved in water. If the product contains organic matter it is clarified. The solution

is slightly acidified with nitric acid and the chlorides precipitated in the form of silver chloride by

means of a solution of silver nitrate. The excess silver nitrate is titrated with a solution of ammonium

thiocyanate, by Volhard's method.

3. REAGENTS

3.1. Solution of ammonium thiocyanate 0.1 N.

3.2. Solution of silver nitrate 0.1 N.

3.3. Saturated solution of ammonium ferric sulphate.

3.4. Nitric acid, d: 1.38.

3.5. Diethyl ether A.R.

3.6. Acetone A.R.

3.7. Carrez I solution: dissolve in water 21.9 g of zinc acetate, Zn (CH 3 COO) 2 · 2H 2 O and 3 g of

glacial acetic acid. Make up to 100 ml with water.

3.8. Carrez II solution: dissolve in water 10·6 g of potassium ferrocynaide K 4 Fe (CN) 6 · 3H 2 O. Make

up to 100 ml with water.

3.9. Active carbon A.R., free from chlorides and not absorbing them.

4. APPARATUS

Mixer (tumbler): approximately 35 to 40 rpm.

5. PROCEDURE

5.1. Preparation of the solution

According to the nature of the sample, prepare a solution as shown under 5.1.1, 5.1.2 or 5.1.3.

At the same time carry out a blank test omitting the sample to be analysed.

5.1.1. Samples free from organic matter

Weigh to the nearest mg a sample of not more than 10 g and containing not more than 3 g

of chlorine in the form of chlorides. Place with 400 ml of water in a 500 ml volumetric

flask at approximately 20 ºC. Mix for thirty minutes in the tumbler, bring up to volume,

homogenise and filter.

5.1.2. Samples containing organic matter, excluding the products listed under 5.1.3.

Weigh approximately 5 g of the sample to the nearest mg and place with1 g of active

carbon in a 500 ml volumetric flask. Add 400 ml of water at approximately 20 ºC and 5

ml of Carrez solution I (3.7), stir then add 5 ml of Carrez solution II (3.8). Mix for thirty

minutes in the tumbler, bring up to volume, homogenise and filter.

5.1.3. Cooked feeding-stuffs, flax cakes and flour, products rich in flax flour and other products

rich in mucilage or in colloidal substances (for example, dextrinated starch)

Prepare the solution as described under 5.1.2 but do not filter. Decant (if

necessary centrifuge), remove 100 ml of the supernatant liquid and transfer to a 200 ml

measuring flask. Mix with acetone (3.6) and bring up to volume with this solvent,

homogenise and filter.

5.2. Titration

Using a pipette, transfer to an Erlenmayer flask from 25 ml to 100 ml of the filtrate (according to

the assumed chlorine content) obtained as described under 5.1.1, 5.1.2 or 5.1.3. The aliquot

portion must not contain more than 150 mg of chlorine (C l). Dilute if necessary to not less than

50 ml with water, add 5 ml of nitric acid (3.4.), 20 ml of saturated solution of ammonium ferric

sulphate (3.3) and two drops of ammonium thiocyanate solution (3.1) transferred by means of a

burette filled up to the zero mark. Using a burette, transfer the silver nitrate solution (3.2) in such

a way that an excess of 5 ml is obtained. Add 5 ml of diethyl ether (3.5) and shake hard to

coagulate the precipitate.

Titrate the excess silver nitrate with the ammonium thiocyanate solution (3.1) until the reddish-

brown tint has lasted for one minute.

6. CALCULATION OF RESULTS

The amount of chlorine (w), expressed as sodium chloride, present in the volume of filtrate taken for

titration is calculated by using the following formula

W = 5·845 (V 1 - V 2 ) mg

where: V 1 = ml of silver nitrate solution C·1 N added

V 2 = ml of ammonium thiocyanate solution 0·1 N used for titration.

If the blank test indicates that silver nitrate solution 0·1 N has been consumed deduct this value from

the volume (V 1 - V 2 ).

7. OBSERVATIONS

7.1. Titration may also be carried out by potentiometry;

7.2. In the case of products which are very rich in oils and fats, first de-fat with diethyl ether or light

petroleum;

7.3. In the case of fish-meal, titration may be carried out by Mohr's method.

DETERMINATION OF LACTOSE

1. PURPOSE AND SCOPE

This method makes it possible to determine the level of lactose in feedingstuffs containing more than

0·5% of lactose.

2. PRINCIPLE

The sugars are dissolved in water. The solution is subjected to fermentation by the yeast

Saccharomyces cerevisiae which leaves the lactose intact. After clarification and filtration the lactose

content of the filtrate is determined by the Luff-Schoorl method.

3. REAGENTS

3.1. Suspension of Saccharomyces cerevisiae: suspend 25 g of fresh yeast in 100 ml of water. The

suspension will keep for a maximum period of one week in a refrigerator.

3.2. Carrez solution I: dissolve in water 21·9 g of zinc acetate Zn (CH 3 COO) 2 · 2H 2 O and 3 g of

glacial acetic acid. Make up to 100 ml with water.

3.3. Carrez solution II: dissolve in water 10·6 g of potassium ferrocyanide K 4 Fe (CN) 6 · 3H 2 O. Make

up to 100 ml with water.

3.4. Luff-Schoorl reagent

Stirring carefully, pour the citric acid solution (3.4.2) into the sodium carbonate solution (3.4.2).

Add the copper sulphate solution (3.4.1) and make up to 1 litre with water. Leave to settle

overnight and filter. Check the normality of the reagent thus obtained (Cu 0·1 N; Na 2 CO 3 2N).

The solution's pH should be approximately 9·4.

3.4.1. Copper sulphate solution: dissolve 25 g of copper sulphate A.R. Cu SO 4 5H 2 O, free from

iron, in 100 ml of water.

3.4.2. Citric acid solution: dissolve 50 g of citric acid A.R. C 6 H 8 O 7 · H 2 O in 50 ml of water.

3.4.3. Sodium carbonate solution: dissolve 143·8 g of anhydrous sodium carbonate A.R. in

approximately 300 ml of warm water. Leave to cool.

3.5. Granulated pumice stone boiled in hydrochloric acid, washed in water and dried.

3.6. 30% solution (w/v) of sodium iodide.

3.7. Sulphuric acid 6 N.

3.8. Solution of sodium thiosulphate 0·1 N.

3.9. Starch solution: add a mixture of 5 g of soluble starch in 30 ml of water to 1 litre of boiling

water. Boil for three minutes, leave to cool, and if necessary add 10 mg of mercuric iodide as a

preservative.

4. APPARATUS

Water bath with thermostat set at 38-40 ºC.

5. PROCEDURE

Weigh 1 g of the sample to the nearest mg and place this portion of the sample in a 100 ml volumetric

flask. Add 25 to 30 ml of water. Place the flask in a boiling water bath for thirty minutes and then cool

to approximately 35 ºC. Add 5 ml of yeast suspension (3·1) and homogenise. Leave the flask to stand

for two hours in a water bath, at a temperature of 38- 40 ºC. Cool to approximately 20 ºC.

Add 2·5 ml of Carrez solution I (3.2) and stir for thirty seconds, then add 2·5 ml of Carrez solution II

(3.3) and again stir for thirty seconds. Make up to 100 ml with water, mix and filter. Using a pipette,

remove an amount of filtrate which does not exceed 25 ml and which preferably contains from 40 to

80 mg of lactose and transfer it to a 300 ml Erlenmeyer flask. If necessary, make up to 25 ml with

water.

Carry out a blank test in the same way with 5 ml of yeast suspension (3.1).

Determine the lactose content according to Luff-Schoorl, as follows: add exactly 25 ml of Luff-

Schoorl reagent (3.4) and two granules of pumice stone (3.5). Stir by hand-while heating over a free

flame of medium height and bring the liquid to the boil in approximately two minutes. Place the

Erlenmeyer immediately on an asbestos-coated wire gauze with a hole approximately 6 cm in diameter

under which a flame has been lit. The flame shall be regulated in such a way that only the base of the

Erlenmeyer is heated. Fit a reflux condenser to the Erlenmeyer flask. Boil for exactly ten minutes.

Cool immediately in cold water and after approximately five minutes titrate as follows

Add 10 ml of potassium iodide solution (3.6) and immediately afterwards (carefully, because of the

risk of abundant foaming) add 25 ml of sulphuric acid 6 N (3.7). Titrate with sodium thiosulphate

solution 0·1 N (3.8) until a dull yellow colour appears, add the starch indicator (3.9) and complete

titration.

Carry out the same titration on an accurately measured mixture of 25 ml of Luff-Schoorl reagent (3.4)

and 25 ml of water, after adding 10 ml of potassium iodide solution (3.6) and 25 ml of sulphuric acid 6

N (3.7) without boiling.

6. CALCULATION OF RESULTS

Using the attached table, establish the amount of lactose in mg which corresponds to the difference

between the results of the two titrations, expressed in ml of sodium thiosulphate 0·1 N.

Express the result as parts of anhydrous lactose as a percentage of the sample.

7. OBSERVATION

For products containing more than 40% of fermentable sugar, use more than 5 ml of yeast suspension

(3.1).

Table of values for 25 ml of Luff-Schoorl reagent

ml of Na 2 S 2 O 3 0·1 N, two minutes' heating, ten minutes' boiling

Na 2 S 2 O 3 0·1

Glucose, fructose invert

Lactose

Maltose

Na 2 S 2 O 3

N

sugars

G 12 H 22 O 11

C 12 H 22 O 11

0·1 N

ml

mg

difference

mg

difference

mg

difference

ml

2.4

2.4

3.6

3.7

3.9

3.9

4.8

2.4

7.3

3.7

7.8

3.9

7.2

2.5

11. 0 3.7 11.7 3.9 9.7 2.5

14. 7 3.7

15. 6 4.0 12.2 2.5

18. 4 3.7

19. 6 3.9 14.7 2.5

22. 1 3.7

23. 5 4.0 17.2 2.6

25. 8 3.7

27. 5 4.0 19.8 2.6

29. 5 3.7

31. 5 4.0 22.4 2.6

33. 2 3.8

35. 5 4.0 25.0 2.6

37. 0 3.8

39. 5 4.0 25.0 2.4 37.0 3.8 39.5 4.0 30.3 2.7

44. 6 3.8

47. 5 4.1 33.0 2.7

48. 4 3.8

51. 6 4.1 35.7 2.8

52. 2 3.8

55. 7 4.1 38.5 2.8

56. 0 3.9

59. 8 4.1 41.3 2.9 59.9 3.9

63. 9 4.1 44.2 2.9 63.8 3.9

68. 0 4.2 47.1 2.9 67.7 4.0

72. 2 4.3 50.0 3.0 71.7 4.0

76. 5 4.4 53.0 3.0 75.7 4.1

80. 9 4.5 56.0 3.1 79.8 4.1

85. 4 4.6 59.1 3.1 83.9 4.1

90. 0 4.6 62.2 88.0

6

10. DETERMINATION OF POTASSIUM

1. PURPOSE AND SCOPE

This method makes it possible to determine the level of potassium in feeding-stuffs.

2. PRINCIPLE

The sample is ashed and the ash dissolved in hydrochloric acid. The potassium content of the solution

is determined by flame photometry in the presence of caesium chloride and aluminium nitrate. The

addition of these substances largely eliminates interference from disturbing elements.

3. REAGENTS

3.1. Hydrochloric acid A.R., d: 1.12.

3.2. Caesium chloride A.R.

3.3. Aluminium nitrate Al (NO 3 ) 3 · 9 H 2 O, general purpose reagent.

3.4. Potassium chloride A.R., anhydrous.

3.5. Loading agent: dissolve in water 50 g of caesium chloride (3.2) and 250 g of aluminium nitrate

(3.3), make up to 1 litre with water and homogenise. Store in plastic bottles.

3.6. Standard solution of potassium: dissolve in water 1·907 g of potassium chloride (3.4), add 5 ml

of hydrochloric acid (3.1), make up to 1 litre with water and homogenise. Store in plastic bottles.

1 ml of this solution contains 1·00 mg of potassium

4. APPARATUS

4.1. Platinum, silica or porcelain crucibles for ashing, provided if necessary with lids.

4.2. Electric muffle-furnace with thermostat.

4.3. Flame photometer.

5. PROCEDURE

5.1. Analysis of sample

As a general rule, weigh out 10 g of the sample to the nearest 10 mg, place in a crucible and ash

at 450 ºC for three hours. After cooling transfer the ash quantitatively to a 500 ml graduated

flask, using 250 to 300 ml of water and then 50 ml of hydrochloric acid (3.1). When all release

of carbon dioxide has ceased, heat the solution and keep at a temperature of about 90 ºC for two

hours, stirring occasionally. After cooling to room temperature, make up to the mark with water,

shake and filter. Transfer to a 100 ml graduated flask an aliquot part of the filtrate containing a

maximum of 1·0 mg of potassium, add 10·0 ml of loading agent (3.5), make up to the mark with

water and homogenise. In the case of higher levels of potassium dilute the solution to be

analysed in suitable proportions before adding the loading agent.

The table below is given as a guide for a sample of about 10 g.

Assumed potassium content of

Dilution factor

Aliquot part in ml of the solution

the sample (% K)

up to 0·1

—

0·1 to 0·5

—

0·5 to 1·0

—

1·0 to 5·0

1: 10

5·0 to 10·0

1: 10

10·0 to 20·0

1: 20

Measure by flame photometry at a wavelength of 768 nm. Calculate the result by means of a

calibration curve.

5.2. Calibration curve

Place exactly 10 ml of the standard solution (3.6) in a 250 ml graduated flask, make up to the

mark with water and homogenise. Place in 100 ml graduated flasks exactly 5, 10, 15, 20 and 25

ml of this solution, corresponding respectively to amounts of potassium of 0·2, 0·4, 0·6, 0·8 and

1·0 mg. Complete the series with a blank flask containing no standard solution. Add 10 ml of

loading agent (3.5) to each flask, make up to the mark with water and homogenise. Carry out the

measurements as indicated in 5.1. The calibration curve is generally linear up to a potassium

concentration of 1 mg in 100 ml of solution.

6. CALCULATION OF RESULTS

Express the result as a percentage of the sample.

7. OBSERVATIONS

It is not always necessary to add loading agent (3.5) in order to eliminate the interference of disturbing

elements.

11. DETERMINATION OF SODIUM

1. PURPOSE AND SCOPE

This method makes it possible to determine the level of sodium in feedings stuffs.

2. PRINCIPLE

The sample is ashed and the ash dissolved in hydrochloric acid. The sodium content of the solution is

determined by flame photometry in the presence of caesium chloride and aluminium nitrate. The

addition of these substances largely eliminates interference from disturbing elements.

3. REAGENTS

3.1. Hydrochloric acid A.R., d: 1.12.

3.2. Caesium chloride A.R.

3.3. Aluminium nitrate Al (NO 3 ) 3 · 9 H 2 O, general purpose reagent

3.4. Sodium chloride A.R., anhydrous.

3.5. Loading agent: dissolve in water 50 g of caesium chloride (3.2) and 250 g of aluminium nitrate

(3.3), make up to 1 litre with water and homogenise. Store in plastic bottles.

3.6. Standard solution of sodium: dissolve in water 2·542 g of sodium chloride (3.4), add 5 ml of

hydrochloric acid (3.1), make up to 1 litre with water and homogenise Store in plastic bottles, 1

ml of this solution contains 1·00 mg of sodium.

4. APPARATUS

4.1. Platinum, silica or porcelain crucibles for ashing, provided if necessary with lids.

4.2. Electric muffle-furnace with thermostat.

4.3. Flame photometer.

5. PROCEDURE

5.1. Analysis of sample

As a general rule, weigh out 10 g of the sample to the nearest 10 mg, place in a crucible (4.2) and

ash at 450 ºC for three hours. Avoid overheating (ignition). After cooling transfer the ash

quantitatively to a 500 ml graduated flask, using 250 to 300 ml of water and then 50 ml of

hydrochloric acid (3.1). When all release of carbon dioxide has ceased, heat the solution and

keep at a temperature of about 90 ºC for two hours, stirring occasionally. After cooling to room

temperature, make up to the mark with water, shake and filter. Transfer to a 100 ml graduated

flask an aliquot part of the filtrate containing a maximum of 1·0 mg of sodium, add 10·0 ml of

loading agent (3.5), make up to the mark with water and homogenise. In the case of higher levels

of sodium, dilute the solution to be analysed in suitable proportions before adding the loading

agent.

The table below is given as a guide for a sample of about 10 g.

Assumed sodium content of the

Dilution factor

Aliquot part in ml of the solution

sample (% K)

up to 0·1

—

0·1 to 0·5

—

0·5 to 1·0

—

1·0 to 5·0

1: 10

5·0 to 10·0

1: 10

10·0 to 20·0

1: 20

Measure by flame photometry at a wavelength of 589 nm. Calculate the result by means of a

calibration curve.

5.2. Calibration curve

Place exactly 10 ml of the standard solution (3.6) in a 250 ml graduated flask, make up to the

mark with water and homogenise. Place in 100 ml graduated flasks exactly 5, 10, 15, 20 and 25

ml of this solution, corresponding respectively to amounts of sodium of 0·2, 0·4, 0·6, 0·8 and 1·0

mg. Complete the series with a blank flask containing no standard solution. Add 10 ml of

loading agent (3.5) to each flask, make up to the mark with water and homogenise. Carry out the

measurements as indicated in 5.1. The calibration curve is generally linear up to a sodium

concentration of 1 mg in 100 ml of solution.

6. CALCULATION OF RESULTS

Express the result as a percentage of the sample.

7. Observations

7.1. For products containing more than 4% of sodium, it is preferable to ash the substance for two

hours in a crucible with a lid. After cooling, add water, bring the ash into suspension by means of

a platinum wire, dry and ash again for two hours in the crucible with a lid.

7.2. If the sample consists solely of mineral substances, dissolve without prior ashing.

12. DETERMINATION OF SUGAR

1. PURPOSE AND SCOPE

This method makes it possible to determine the amount of reducing sugars and total sugars after

inversion, expressed as glucose or where appropriate as sucrose, converting by the factor 0·95. It is

applicable to compound feeding-stuffs. Special methods are provided for other feeding-stuffs. Where

necessary, lactose should be measured separately and taken into account when calculating the results.

2. PRINCIPLE

The sugars are extracted in dilute ethanol; the solution is clarified with Carrez solutions I and II. After

eliminating the ethanol, the quantities before and after inversion are determined by the Luff-Schoorl

method.

3. REAGENTS

3.1. 40% ethanol (v/v) d: 0·948 at 20 ºC, neutralised to phenolphthalein.

3.2. Carrez solution I: dissolve in water 21·9 g of zinc acetate Zn (CH 3 COO) 2 · 2H 2 O and 3 g of

glacial acetic acid. Make up to 100 ml with water.

3.3. Carrez solution II: dissolve in water 10·6 g of potassium ferrocyanide K 4 Fe (CN) 6 · 3H 2 O. Make

up to 100 ml with water.

3.4. 0·1% solution (w/v) of methyl orange.

3.5. Hydrochloric acid 4 N.

3.6. Hydrochloric acid 0·1 N.

3.7. Sodium hydroxide solution 0·1 N.

3.8. Luff-Schoorl reagent

Stirring carefully, pour the citric acid solution (3.8.2) into the sodium carbonate solution (3.8.3).

Add the copper sulphate solution (3.8.1) and make up to 1 litre with water. Leave to settle

overnight and filter. Check the normality of the reagent thus obtained (Cu 0·1 N; Na 2 CO 3 2 N).

The solution's pH should be approximately 9·4.

3.8.1. Copper sulphate solution: dissolve 25 g of copper sulphate A.R., Cu SO 4 · 5H 2 O, free

from iron, in 100 ml of water.

3.8.2. Citric acid solution: dissolve 50 g of citric acid A.R., C 6 H 8 O 7 H 2 O in 50 ml of water.

3.8.3. Sodium carbonate solution: dissolve 143·8 g of anhydrous sodium carbonate A.R. in

approximately 300 ml of warm water. Leave to cool.

3.9. Sodium thiosulphate solution 0·1 N

3.10. Starch solution: add a mixture of 5 g of soluble starch in 30 ml of water to 1 litre of boiling

water. Boil for three minutes, leave to cool and if necessary add 10 mg of mercuric iodide as a

preservative.

3.11. Sulphuric acid 6 N.

3.12. 30% solution (w/v) of potassium iodide.

3.13. Granulated pumice stone boiled in hydrochloric acid, washed in water and dried.

3.14. 3-methylbutan-l-ol.

4. APPARATUS

Mixer (tumbler): approximately 35 to 40 rpm.

5. PROCEDURE

5.1. Extraction of sample

Weigh 2.5 g of the sample to the nearest mg and place in a 250 ml volumetric flask. Add 200 ml

of ethanol (3.1) and mix in the tumbler for one hour. Add 5 ml of Carrez solution I (3.2) and stir

for one minute. Add 5 ml of Carrez solution II (3.3) and again stir for one minute. Make up to

volume with ethanol (3.1), homogenise and filter. Remove 200 ml of the filtrate and evaporate to

approximately half volume in order to eliminate most of the ethanol. Transfer the evaporation

residue quantitatively to a 200 ml volumetric flask using warm water, cool, bring up to volume

with water, homogenise and filter if necessary. This solution will be used to determine the

amount of reducing sugars and, after inversion, of total sugars.

5.2. Determination of reducing sugars

Using a pipette, remove not more than 25 ml of the solution containing less than 60 mg of

reducing sugars expressed as glucose. If necessary, make up to 25 ml with distilled water and

determine the content of reducing sugars by the Luff-Schoorl method. The result is expressed as

the percentage content of glucose in the sample.

5.3. Determination of total sugars after inversion

Using a pipette take 50 ml of the solution and transfer to a 100 ml volumetric flask. Add a few

drops of methyl orange solution (3.4) then, carefully and stirring continuously, add hydrochloric

acid 4 N (3.5) until the liquid turns a definite red. Add 15 ml of hydrochloric acid 0·1 N (3.6),

immerse the flask in a fast boiling water bath and keep there for thirty minutes. Cool rapidly to

approximately 20 ºC and add 15 ml of sodium hydroxide solution 0·1 N (3.7). Make up to 100

ml with water and homogenise. Remove not more than 25 ml containing less than 60 mg of

reducing sugars expressed as glucose. If necessary, make up to 25 ml with distilled water and

determine the content of reducing sugars by the Luff-Schoorl method. The result is expressed as

the percentage of glucose or, where appropriate, sucrose, by multiplying by the factor 0·95.

5.4. Titration by the Luff-Schoorl method

Using a pipette, take 25 ml of Luff-Schoorl reagent (3.8) and transfer to a 300 ml Erlenmeyer

flask; add exactly 25 ml of the clarified sugar solution. Add 2 granules of pumice stone (3.13),

heat, stirring by hand, over a free flame of medium height and bring the liquid to the boil in

approximately two minutes. Place the Erlenmeyer immediately on an asbestos-coated wire gauze

with a hole approximately 6 cm in diameter under which a flame has been lit. The flame shall be

regulated in such a way that only the base of the Erlenmeyer is heated. Fit a reflux condenser to

the Erlenmeyer flask, Boil for exactly ten minutes. Cool immediately in cold water and after

approximately five minutes titrate as follows

Add 10 ml of potassium iodide solution (3.12) and immediately afterwards (carefully, because of

the risk of abundant foaming), add 25 ml of sulphuric acid 6 N (3.11). Titrate with sodium

thiosulphate solution 0·1 N (3.9) until a dull yellow colour appears, add the starch indicator

(3.10) and complete titration.

Carry out the same titration on an accurately measured mixture of 25 ml of Luff-Schoorl reagent

(3.8) and 25 ml of water, after adding 10 ml of potassium iodide solution (3.12) and 25 ml of

sulphuric acid 6 N (3.11) without boiling.

6. CALCULATION OF RESULTS

Using the table establish the amount of glucose in mg which corresponds to the difference between the

values of the two titrations, expressed in mg of sodium thiosulphate 0·1 N.

Express the result as a percentage of the sample.

7. SPECIAL PROCEDURES

7.1. In the case of feeding-stuffs which are rich in molasses and other feeding-stuffs which are not

particularly homogeneous, weigh out 20 g and place with 500 ml of water in a 1 litre volumetric

flask. Mix for one hour in the tumbler. Clarify using Carrez 1 (3.2) and II (3.3) reagents as

described under 5.1, this time however using four times the quantities of each reagent. Bring up

to volume with 80% ethanol (v/v).

Homogenise and filter. Eliminate the ethanol as described under 5.1. If there is no dextrinised

starch, bring up to volume with distilled water.

7.2. In the case of molasses and straight feeding-stuffs which are rich in sugar and almost starch-free

(carobs, dried beetroot cossettes etc.), weigh out 5 g, place in a 250 ml volumetric flask, add 200

ml of distilled water and mix in the tumbler for one hour, or more if necessary. Clarify using

Carrez I (3.2) and II (3.3) reagents as described under 5.1. Bring up to volume with cold water,

homogenise and filter. In order to determine the amount of total sugars, continue as described

under 5.3.

8. OBSERVATIONS

8.1. In order to prevent foaming it is advisable to add (irrespective of the volume) approximately 1

ml of 3-methylbutan-l-ol (3.14) before boiling with Luff-Schoorl reagent.

8.2. The difference between the content of total sugars after inversion, expressed as glucose, and the

content of reducing sugars, expressed as glucose, multiplied by 0·95, gives the percentage

content of sucrose.

8.3. In order to determine the content of reducing sugars, excluding lactose, two methods may be

adopted

8.3.1. for an approximate calculation, multiply by 0·675 the lactose content established by a

different method of analysis and subtract the result obtained from the content of reducing

sugars.

8.3.2. For an accurate calculation of reducing sugars, excluding lactose, the same sample must

be used for the two final determinations. One of the analyses is carried out on part of the

solution obtained under 5.1, the other on part of the solution obtained during the

determination of lactose by the method laid down for that purpose (after fermenting the

other types of sugar and clarifying).

In both cases the amount of sugar present is determined by the Luff-Schoorl method and

calculated in mg of glucose. One of the values is subtracted from the other and the difference is

expressed as a percentage of the sample.

Example

The two volumes taken correspond, for each determination, to a sample of 250 mg.

In the first case 17 ml of sodium thiosulphate solution 0·1 N corresponding to 44·2 mg of glucose

is consumed; in the second, 11 ml, corresponding to 27·6 mg of glucose.

The difference is 16·6 mg of glucose.

The content of reducing sugars (excluding lactose), calculated as glucose, is therefore

4 x 16 x 6

= 6.64%

Table of values for 25 ml of Luff Schoorl reagent

Na 2 S 2 O 3

Glucose, fructose invert

Lactose

Maltose

Na 2 S 2 O 3

0·1 N

sugars

G 12 H 22 O 11

C 12 H 22 O 11

0·1 N

mg

difference

mg

difference

mg

difference

ml

2.4

2.4

3.6

3.7

3.9

3.9

4.8

2.4

7.3

3.7

7.8

3.9

7.2

2.5

11.0

3.7

11.7

3.9

9.7

2.5

14.7

3.7

15.6

4.0

12.2

2.5

18.4

3.7

19.6

3.9

14.7

2.5

22.1

3.7

23.5

4.0

17.2

2.6

25.8

3.7

27.5

4.0

19.8

2.6

29.5

3.7

31.5

4.0

22.4

2.6

33.2

3.8

35.5

4.0

25.0

2.6

37.0

3.8

39.5

4.0

27.6

2.7

40.8

3.8

43.5

4.0

30.3

2.7

44.6

3.8

47.5

4.1

33.0

2.7

48.4

3.8

51.6

4.1

35.7

2.8

52.2

3.8

55.7

4.1

38.5

2.8

56.0

3.9

59.8

4.1

41.3

2.9

59.9

3.9

63.9

4.1

44.2

2.9

63.8

3.9

68.0

4.2

47.1

2.9

67.7

4.0

72.2

4.3

50.0

3.0

71.7

4.0

76.5

4.4

53.0

3.0

75.7

4.1

80.9

4.5

56.0

3.1

79.8

4.1

85.4

4.6

59.1

3.1

83.9

4.1

90.0

4.6

62.2

88.0

94.6

14. DETERMINATION OF UREA

1. PURPOSE AND SCOPE

This method makes it possible to determine the level of urea in feedingstuffs.

2. PRINCIPLE

The sample is suspended in water with a clarifying agent. The suspension is filtered. The urea content

of the filtrate is determined after the addition of 4-dimethylaminobenzaldehyde (4-DMAB) by

measuring the optical density at a wavelength of 420 nm,

3. REAGENTS

3.1. Solution of 4-dimethylaminobenzaldehyde: dissolve 1·6 g of 4-DMAB A.R. in 100 ml of 96%

ethanol and add 10 ml of hydrochloric acid A.R. (d: 1·19). This reagent keeps for a maximum

period of two weeks.

3.2. Carrez solution I: dissolve in water 21·9 g of zinc acetate Zn (CH 3 COO) 2 · 2H 2 O and 3 g of

glacial acetic acid. Make up to 100 ml with water.

3.3. Carrez solution II: dissolve in water. 10·6 g of potassium ferrocyanide, K 4 Fe (CN) 6 · 3H 2 O.

Make up to 100 ml with water.

3.4. Active carbon A.R. which does not absorb urea (to be checked).

3.5. 0·1% solution (w/v) of urea A.R.

4. APPARATUS

4.1. Mixer (tumbler): approximately 35 to 40 rpm.

4.2. Test tubes: 160 × 16 mm with ground-glass stoppers.

4.3. A spectrophotometer.

5. PROCEDURE

5.1. Analysis of sample

Weigh out 2 g of the sample to the nearest mg and place with 1 g of active carbon (3.4) in a 500

ml volumetric flask. Add 400 ml of water and 5 ml of Carrez solutions I (3.2) and II (3.3). Mix

for thirty minutes in the tumbler. Make up to volume with water, shake and filter.

Remove 5 ml of the transparent colourless filtrates, place in test tubes with ground-glass

stoppers, add 5 ml of 4-DMAB solution (3.1) and mix. Place the tubes in a hot-water bath at 20

ºC. After fifteen minutes measure the optical density of the sample solution with the

spectrophotometer at 420 nm. Compare with the blank test solution of the reagents.

5.2. Calibration Curve

Remove volumes of 1, 2, 4, 5 and 10 ml of the urea solution (3.5), place in 100 ml volumetric

flasks and make up the volume with water. Remove 5 ml from each solution, add 5 ml of 4-

DMAB solution (3.1) to each of them, homogenise and measure the optical density as shown

above in comparison with a control solution containing 5 ml of 4-DMAB and 5 ml of water free

from urea. Plot the calibration curve.

6. CALCULATION OF RESULTS

Determine the amount of urea in the sample using the calibration curve.

Express the result as a percentage of the sample.

7. OBSERVATIONS

7.1. In the case of contents of urea exceeding 3%, reduce the sample to 1 g or dilute the original

solution so that there are not more than 50 mg of urea in 500 ml.

7.2. In the case of low contents of urea, increase the sample as long as the filtrate remains transparent

and colourless.

7.3. If the sample contains simple nitrogenous compounds such as amino acids, the optical density

should be measured at 435 nm.

16. ESTIMATION OF THE UREASE ACTIVITY OF PRODUCTS DERIVED FROM SOYA

1. PURPOSE AND SCOPE

This test makes it possible estimate the urease activity of products derived from soya and to show

whether these products have been cooked for a sufficient length of time.

2. PRINCIPLE

Urease activity is estimated by the amount of ammoniacal nitrogen liberated per 1 g of product per

minute at 30 ºC from a solution of urea.

3. REAGENTS

3.1. Hydrochloric acid 0·1 N

3.2. Solution of sodium hydroxide 0·1 N.

3.3. 3.3. Loading agent of phosphate 0·05 M, containing, per 1000 ml, 4·45 g of disodium phosphate

(Na 2 HPO 4 · 2H 2 O) and 3·40 g of monopotassium phosphate (KH 2 PO 4 ).

3.4. Freshly-prepared urea loading agent containing 30·0 g of urea per 1000 ml of loading agent

(3.3); pH 6·9-7·0.

4. APPARATUS

4.1. Potentiometric titration apparatus or high sensitivity pH-meter (0·02 pH) with magnetic stirrer.

4.2. Water bath fitted with thermostat set at 30 ºC exactly.

4.3. Test-tubes with ground-glass stoppers, 150 × 18 mm.

5. PROCEDURE

Crush about 10 g of the sample (for example in a coffee mill) so that it passes through a sieve with a

mesh of 0·2 mm. Weigh out 0·2 g of the crushed sample to the nearest mg, place in a test tube with a

ground-glass stopper and add 10 ml of urea loading agent (3.4). Stopper immediately and shake

vigorously. Place the tube in a water bath set at 30 ºC exactly and keep there for exactly thirty minutes.

Immediately add 10 ml of 0·1 N hydrochloric acid (3.1), cool rapidly to 20 ºC and transfer the contents

of the tube quantitatively to a titration vessel, rinsing twice with 5 ml of water. Using a glass electrode

(4.1) titrate immediately and rapidly to pH 4·7 with the 0·1 N sodium hydroxide solution (3.2) by

electrometry.

Carry out a blank test as follows

Quickly place a sample of 0·2 g weighed to the nearest mg in a test tube with a ground-glass stopper,

add 10 ml of 0·1 N hydrochloric acid (3.1) and then 10 ml of urea loading agent (3.4). Cool the tube

immediately in ice-water and leave there for thirty minutes. Under the conditions indicated above,

transfer the contents of the tube to the titration vessel using the 0·1 N sodium hydroxide solution (3.2)

up to pH 4·7.

6. CALCULATION

The urease activity is calculated by using the formula

mg N

.4 (b – a)

AT 30 ˚C =

g min

30 . E

where

a = ml of 0·1N sodium hydroxide solution consumed by the sample,

b = ml of 0·1N sodium hydroxide solution consumed in the blank test,

E = weight of sample in g.

7. OBSERVATION

7.1. This method is suitable for a urease activity of up to 1 mg of N/g/min at 30 ºC. For more active

products, the size of the sample can be reduced to 50 mg.

7.2. Products containing more than 10% of crude fatty substance must first be defatted cold.

Mitbug[ fl-Istamperija tal-Gvern — Printed at the Government Printing Press