GB/T 20378-2006 PDF English
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Native starch -- Determination of starch content -- Ewers polarimetric method
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GB/T 20378-2006: Native starch -- Determination of starch content -- Ewers polarimetric method---This is an excerpt. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.), auto-downloaded/delivered in 9 seconds, can be purchased online: https://www.ChineseStandard.net/PDF.aspx/GBT20378-2006
GB
NATIONAL STANDARD OF THE
PEOPLE’S REPUBLIC OF CHINA
ICS 67.180.20
X 11
GB/T 20378-2006 / ISO 10520:1997
Native Starch – Determination of Starch Content – Ewers
Polarimetric Method
(ISO 10520:1997, IDT)
ISSUED ON: MARCH 14, 2006
IMPLEMENTED ON: OCTOBER 01, 2006
Issued by: General Administration of Quality Supervision, Inspection and
Quarantine;
Standardization Administration of the People’s Republic of China.
Table of Contents
Foreword ... 3
1 Scope ... 4
2 Normative References ... 4
3 Principle ... 4
4 Reagents ... 5
5 Apparatus ... 5
6 Processing of Sample ... 6
7 Procedure ... 6
8 Expression of Results ... 7
9 Precision ... 8
10 Test Report ... 9
Annex A (Informative) Ewers Method - Collaborative Study 1990 ... 10
Bibliography ... 11
Native Starch – Determination of Starch Content – Ewers
Polarimetric Method
1 Scope
This Standard specifies a polarimetric method for the determination of the starch content of
native starch.
This Standard is not applicable to the determination of starch content in native starch, modified
starch and pregelatinized (cold water soluble) starch with high amylose content.
2 Normative References
The provisions in following documents become the provisions of this Standard through
reference in this Standard. For dated references, the subsequent amendments (excluding
corrigendum) or revisions do not apply to this Standard, however, parties who reach an
agreement based on this Standard are encouraged to study if the latest versions of these
documents are applicable. For undated references, the latest edition of the referenced document
applies.
ISO 1666 Starch – Determination of Moisture Content – Oven-Drying Method
GB/T 6682 Water for Analytical Laboratory Use - Specification and Test Methods
3 Principle
The method includes two intermediate determination steps.
3.1 A portion of the sample is hydrolysed with dilute hydrochloric acid and the optical rotation
measured polarimetrically after clarification and filtration.
3.2 A second portion of the sample is treated with 40 % (V/V) ethanol to extract soluble sugars
and polysaccharides of lower molecular mass. The filtrate is then subjected to the procedure
given in 3.1. The difference between the measurements 3.1 and 3.2, multiplied by a factor, gives
the starch content of the sample.
NOTE: Key parameters of the method are the time and temperature of the hydrolysis, and the correct use
and calibration of the polarimeter. Consequently, the method includes constant agitation in the water bath,
which should be of a size appropriate to ensure rapid temperature rise and steady temperature conditions.
4 Reagents
Use only reagents of recognized analytical grade, unless otherwise specified, and water
complying with grade 2 in accordance with GB/T 6682.
4.1 Dilute hydrochloric acid (HCl) solution
c(HCI) = 7.7 mol/L, dilute 63.7 mL of hydrochloric acid (ρ20 = 1.19 g/mL) with water up to
100mL.
4.2 Dilute hydrochloric acid (HCl) solution
c(HCI) = 0.309 mol/L, dilute 25.6 mL of hydrochloric acid (ρ20 = 1.19 g/ml) with water up to
1000mL.
NOTE: The concentration should be verified using sodium hydroxide solution [c(NaOH) = 0.1 mol/L]
and Methyl red as indicator: 10 mL HCI should consume 30.94 mL of 0.1 mol/L NaOH.
4.3 Dilute ethanol solution
40 % (V/V) (ρ20 = 0.948 g/ml).
4.4 Carrez solution I
Dissolve 10.6 g of potassium hexacyanoferrate (II) trihydrate [K4[Fe(CN)6]•3H2O] in water.
Dilute to 100 mL with water.
4.5 Carrez solution II
Dissolve 21.9 g of zinc acetate dihydrate [Zn(CH3COO)2•2H2O] and 3 g of glacial acetic acid
in water. Dilute to 100 mL with water.
5 Apparatus
5.1 Volumetric flasks, of capacity 100mL.
5.2 Boiling water bath equipped with a vibrator or a magnetic stirrer.
5.3 Polarimeter, adjusted to a wavelength of 589.3 nm, with 200 mm tubes.
5.4 Analytical balance, capable of weighing to the nearest 0.001 g.
6 Processing of Sample
If the particle size of the laboratory sample exceeds 0.5 mm, grind the sample to pass a sieve
with 0.5 mm apertures. Homogenize the sample thus prepared.
7 Procedure
Carry out weighing to the nearest 0.001 g (see 5.4).
7.1 Determination of optical rotation of a total portion
7.1.1 Weigh 2.5 g ± 0.05 g (m1) of the test sample and transfer it to a volumetric flask (5.1).
Add 25 mL of the dilute hydrochloric acid (4.2) and agitate to distribute the test sample evenly.
Add a further 25 mL of the dilute hydrochloric acid (4.2).
7.1.2 Immerse the flask in the boiling water bath and shake continuously or immerse the flask
in the boiling water bath equipped with a magnetic stirrer and stir at minimum speed.
7.1.3 Leave the flask for 15 min ± 5 s in the boiling water bath and stop shaking or stirring
shortly before removing it. Immediately add 30 mL of cold water and cool rapidly under
flowing water to 20 °C ± 2 °C.
7.1.4 Add 5 mL of the Carrez solution I (4.4) and shake for 1 min.
7.1.5 Add 5 mL of the Carrez solution II (4.5) and shake for 1 min.
7.1.6 Dilute to the mark with water. Homogenize and filter the solution through a suitable filter
funnel and paper. If the filtrate is not perfectly clear, repeat the operations with 10 mL of each
of the Carrez solutions.
7.1.7 Measure the optical rotation (α1) of the solution in a 200mm tube with the polarimeter
(5.3).
7.2 Determination of optical rotation of substances soluble in 40 % (V/V) ethanol
7.2.1 Weigh 5 g ± 0.1 g (m2) of the sample and transfer to a 100 mL volumetric flask (5.1). Add
about 80 mL of the ethanol solution (4.3). Leave the flask to stand for 1 h at room temperature;
shake vigorously six times during the hour to ensure thorough mixing of the test sample with
the ethanol. Dilute to 100 mL with ethanol (4.3), homogenize and filter.
7.2.2 Pipette 50 mL of the filtrate (equivalent to 2.5 g of the test portion) into a volumetric flask
(5.1). Add 2.1 mL of the dilute hydrochloric acid (4.1) and shake vigorously. Fit a reflux
condenser to the flask and immerse the flask in a boiling water bath. Remove the flask from the
boiling water bath after 15 min ± 5 s. Cool to 20 °C ± 2 °C.
......
Source: Above contents are excerpted from the full-copy PDF -- translated/reviewed by: www.ChineseStandard.net / Wayne Zheng et al.
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