Soil improvers and growing media - Sampling

This document specifies methods for sampling of soil improvers and growing media for subsequent determination of quality and quantity. It outlines the principles to be taken into consideration when taking the sample and ensuring an adequate quantity is available for testing.
This document applies to material in solid form (including pre-shaped growing media) and liquid form.
This document is intended to be used by manufacturers, buyers and enforcement agencies in verifying claims made for these materials. It is not intended that it should necessarily be used for the purpose of manufacturing control.
The requirements of this document can differ from the national legal requirements for the declaration of the material concerned.

Bodenverbesserungsmittel und Kultursubstrate - Probenahme

Dieses Dokument legt Verfahren für die Probenahme von Bodenverbesserungsmitteln und Kultursubstraten für die anschließende Bestimmung von Qualität und Menge fest. Es führt Regeln auf, die bei der Probenahme zu beachten sind und stellt sicher, dass eine ausreichende Menge für die Untersuchung zur Verfügung steht.
Dieses Dokument gilt für Material in fester Form (einschließlich vorgeformter Kultursubstrate) und in flüssiger Form.
Dieses Dokument ist für Hersteller, Käufer und Vollzugsbehörden für den Nachweis von Anforderungen an diese Materialien vorgesehen. Das festgelegte Verfahren sollte nicht für Kontrollzwecke beim Hersteller verbindlich vorgeschrieben werden.
Die Anforderungen dieses Dokuments können von den nationalen gesetzlichen Vorgaben bezüglich der Deklaration der erwähnten Materialien abweichen.

Amendements du sol et supports de culture - Échantillonnage

Le présent document spécifie des méthodes d’échantillonnage des amendements du sol et des supports de culture qui permettent d’évaluer ultérieurement la qualité et la quantité de ceux-ci. Il indique les principes à prendre en considération pour prélever l’échantillon et pour s’assurer qu’une quantité convenable pour l’essai a été prélevée.
Le présent document s’applique aux matériaux se présentant sous forme solide (y compris les supports de culture préformés) et sous forme liquide.
Le présent document est destiné à être utilisé par les fabricants, les acheteurs et les organismes de contrôle chargés de vérifier les allégations à propos de ces matériaux. Il n’est pas prévu qu’il doive nécessairement être utilisé à des fins de contrôle de fabrication.
Les exigences du présent document peuvent diverger par rapport aux législations nationales en ce qui concerne la déclaration des matériaux concernés.

Izboljševalci tal in rastni substrati - Vzorčenje

General Information

Status
Not Published
Publication Date
13-Sep-2023
Current Stage
4060 - Closure of enquiry - Enquiry
Start Date
06-Apr-2023
Due Date
18-Jan-2022
Completion Date
06-Apr-2023

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SLOVENSKI STANDARD
oSIST prEN 12579:2023
01-januar-2023
Izboljševalci tal in rastni substrati - Vzorčenje
Soil improvers and growing media - Sampling
Bodenverbesserungsmittel und Kultursubstrate - Probenahme
Amendements organiques et supports de culture - Echantillonnage
Ta slovenski standard je istoveten z: prEN 12579
ICS:
65.080 Gnojila Fertilizers
oSIST prEN 12579:2023 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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oSIST prEN 12579:2023

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oSIST prEN 12579:2023


DRAFT
EUROPEAN STANDARD
prEN 12579
NORME EUROPÉENNE

EUROPÄISCHE NORM

January 2023
ICS 65.080 Will supersede EN 12579:2013
English Version

Soil improvers and growing media - Sampling
Amendements organiques et supports de culture - Bodenverbesserungsmittel und Kultursubstrate -
Echantillonnage Probenahme
This draft European Standard is submitted to CEN members for enquiry. It has been drawn up by the Technical Committee
CEN/TC 223.

If this draft becomes a European Standard, CEN members are bound to comply with the CEN/CENELEC Internal Regulations
which stipulate the conditions for giving this European Standard the status of a national standard without any alteration.

This draft European Standard was established by CEN in three official versions (English, French, German). A version in any other
language made by translation under the responsibility of a CEN member into its own language and notified to the CEN-CENELEC
Management Centre has the same status as the official versions.

CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia,
Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway,
Poland, Portugal, Republic of North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Türkiye and
United Kingdom.

Recipients of this draft are invited to submit, with their comments, notification of any relevant patent rights of which they are
aware and to provide supporting documentation.

Warning : This document is not a European Standard. It is distributed for review and comments. It is subject to change without
notice and shall not be referred to as a European Standard.


EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION

EUROPÄISCHES KOMITEE FÜR NORMUNG

CEN-CENELEC Management Centre: Rue de la Science 23, B-1040 Brussels
© 2023 CEN All rights of exploitation in any form and by any means reserved Ref. No. prEN 12579:2023 E
worldwide for CEN national Members.

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Contents Page
European foreword . 5
Introduction . 6
1 Scope . 7
2 Normative references . 7
3 Terms and definitions . 7
4 Requirements . 9
4.1 General . 9
4.2 General requirements for sample taken for microbiological testing . 9
4.3 General requirements for liquid materials . 9
4.4 Moisture content . 9
5 Apparatus . 10
6 Procedure for solid materials . 10
6.1 General . 10
6.2 Location and time of sampling . 11
6.3 Sampling constraints . 11
6.3.1 Limitations on the sampled portion. 11
6.3.2 Number of final samples . 11
6.4 Sampling . 11
6.4.1 Number of sampling points . 11
6.4.2 Distribution of sampling points . 12
6.4.3 Volume of samples . 12
6.4.4 Incremental samples . 12
6.4.5 Microbiological testing . 13
6.5 Final sample . 14
7 Procedure for liquid materials . 14
7.1 General . 14
7.2 Sampling at source . 14
7.3 Homogeneous liquids . 14
7.4 Heterogeneous liquids . 14
7.5 Sampled portion consisting of two or more containers . 15
7.6 Solutions or suspensions in storage vessels of capacity less than 1 000 l . 15
8 Packing and labelling of the final samples. 16
8.1 General . 16
8.2 Labelling . 16
9 Sampling report . 16
10 Dispatch of samples . 17
Annex A (informative) Final sample size required . 18
Annex B (informative) Examples of apparatus for sampling liquid materials . 19
Annex C (informative) Methods of mixing for liquid materials . 30
C.1 General . 30
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C.2 Small containers . 30
C.2.1 Hand shaking . 30
C.2.2 Rocking . 30
C.3 Drums and casks (up to about 1,8 m deep) . 30
C.3.1 Rocking in a see-saw fashion . 30
C.3.2 Rolling to and from . 30
C.3.3 Mechanically driven drum shaker or roller . 30
C.3.4 Mechanical mixing . 30
C.3.5 Hand mixing . 32
C.3.6 Compressed gas . 33
C.4 Shallow tanks . 33
C.5 Deep tanks . 34
C.5.1 General . 34
C.5.2 Pumped circulation . 34
C.5.3 Compressed gas . 34
C.6 Precautions for sampling multi-phase liquids, including slurries . 34
C.7 Precautions for sampling liquids with significant vapour pressure . 35
C.7.1 Introduction. 35
C.7.2 General precautions . 35
C.7.3 Gases liquefied by pressure at ambient temperatures . 35
C.8 Precautions against static electricity . 35
C.8.1 Warning statement . 35
C.8.2 Generation of static electricity. 35
C.8.3 Discharge of static electricity . 36
Annex D (informative) Schematic overview from the sampling procedure . 37
Annex E (informative) Procedure for sampling bulk material . 39
E.1 Procedure for sampling bulk material: Step 1 . 39
E.2 Procedure for sampling bulk material: Step 2 . 39
E.3 Procedure for sampling bulk material: Step 3 . 39
E.4 Procedure for sampling bulk material: Step 4 . 40
E.5 Procedure for sampling bulk material: Step 5 . 40
E.6 Procedure for sampling bulk material: Step 6 . 40
Annex F (informative) Procedure for sampling packaged material . 41
F.1 Procedure for sampling packaged material. Step 1 . 41
F.2 Procedure for sampling packaged material. Step 2 . 41
F.3 Procedure for sampling packaged material. Step 3 . 41
F.4 Procedure for sampling packaged material. Step 4 . 41
3

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F.5 Procedure for sampling packaged material. Step 5. 42
F.6 Procedure for sampling packaged material. Step 6. 42
Bibliography. 43

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prEN 12579:2022 (E)
European foreword
This document (prEN 12579:2022) has been prepared by Technical Committee CEN/TC 223 “Soil
improvers and growing media”, the secretariat of which is held by NEN.
This document is currently submitted to the CEN Enquiry.
This document will supersede EN 12579:2013.
In comparison with the previous edition EN 12579:2013, the following technical modifications have been
made:
— requirements for liquid materials are added to the scope and the sampling procedure;
— requirements for sampling for microbiological testing have been added;
— addition of the following annexes: Annex B (informative) with examples of apparatus for sampling
liquid materials, Annex C (informative) with methods of mixing for liquid materials, Annex D
(informative) with a schematic overview from the sampling procedure, Annex E (informative) about
the procedure for sampling bulk material, and Annex F (informative) about the procedure for
sampling packaged material.
This document has been prepared under a Standardization Request given to CEN by the European
Commission and the European Free Trade Association.

5

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Introduction
Soil improvers and growing media are very difficult to sample because of the variety of materials used
and the inhomogeneous materials involved. When packed some of them are also by their nature and the
packaging and palletisation process subject to pressure which results in various degrees of compression
which need to be counteracted prior to sampling.
The task is further complicated by the variety of sampling equipment that can be used, the quantity to be
represented by the sample and the degree of precision required bearing in mind the cost of testing.
This document gives a sampling method to overcome these difficulties. A suitably competent person
should undertake this sampling.

6

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1 Scope
This document specifies methods for sampling of soil improvers and growing media for subsequent
determination of quality and quantity. It outlines the principles to be taken into consideration when
taking the sample and ensuring an adequate quantity is available for testing.
This document applies to material in solid form (including pre-shaped growing media) and liquid form.
This document is intended to be used by manufacturers, buyers and enforcement agencies in verifying
claims made for these materials. It is not intended that it should necessarily be used for the purpose of
manufacturing control.
The requirements of this document can differ from the national legal requirements for the declaration of
the material concerned.
2 Normative references
The following documents are referred to in the text in such a way that some or all of their content
constitutes requirements of this document. For dated references, only the edition cited applies. For
undated references, the latest edition of the referenced document (including any amendments) applies.
1
EN 13040:— , Soil improvers and growing media — Sample preparation for chemical and physical tests,
determination of dry matter content, moisture content and laboratory compacted bulk density
3 Terms and definitions
For the purposes of this document, the terms and definitions given in CEN/TS 17732:2022 and the
following apply.
3.1
batch
lot
quantity of goods manufactured by the same process under the same conditions, at the same time, and
labelled in the same manner and assumed to have the same characteristics to be sampled using a
particular sampling plan
3.2
consignment
quantity of goods dispatched or received at one time and covered by a particular contract or shipping
document
Note 1 to entry: A consignment may be composed of a part of a batch (lot) or one or more batches (lots) of the same
material or different materials.
3.3
sampled portion
maximum quantity of material from the same batch from which one representative combined sample or
segment samples (for microbiological testing) are taken
3.4
sampling point
defined place from which the incremental sample is taken
3.5
incremental sample
quantity of material taken from one sampling point
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3.6
combined sample
combination of all incremental samples taken from one sampled portion
Note 1 to entry: Combined sample is referred to as aggregate sample in EN 1482-1:2007.
3.7
final sample

representative part of the combined sample taken from the sampled portion obtained, where necessary,
by a process of reduction
3.8
laboratory sample
representative part of the final sample prepared for testing or for microbiological testing the segment
samples
3.9
segment
part of the sampled portion from which a segment sample is taken for microbiological testing
3.10
segment sample
combination of all incremental samples taken from one segment for microbiological testing and is to be
used as a laboratory sample
Note 1 to entry: There will be five segment samples taken from each sampled portion for Fertilising Product
Regulation (FPR) purposes.
3.11
bulk material
material that is not packaged
3.12
package
container and materials contained therein which are delivered and where the packaging remains with
the material after delivery
Note 1 to entry: A package may be a container of loose-filled sack typically up to 100 l, a compressed block or bale
3
and even a ‘big bale’, typically of 4 m . Also plugs in trays are considered to be a package.
3.13
solid form
form characterised by structural rigidity and resistance to changes of shape or volume and in which the
atoms are tightly bound to each other, either in a regular geometric lattice (crystalline solids) or in an
irregular manner (an amorphous solid)
Note 1 to entry: Either in a regular geometric lattice (crystalline solids) or in an irregular manner (an amorphous
solid).
3.14
liquid form
suspension or solution
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4 Requirements
4.1 General
Any final sample collected shall be considered to be representative of the whole of the material of the
sampled portion.
Special care shall be taken to ensure that all sampling apparatus is clean, dry, and made from material
which will not contaminate the sample. It shall be adapted to the batch size, the aggregate state and the
particle size and nature of the substances. Sampling shall be in such a manner as to preserve the quantity
and quality aspects for which the sample will be tested.
4.2 General requirements for sample taken for microbiological testing
Sampling equipment shall be either unused or have been subject to a sterilization process before use. To
avoid cross contamination, a fresh set of unused or sterilized equipment or other appropriate steps shall
be used to obtain each individual segment sample.
When using new, unopened plastic bags, the bags do not need sterilization.
Contact with human skin or liquids shall be prevented in case of sampling for human pathogens.
Take segment samples of at least 1 l or 200 g (the material will have the moisture content as received)
and deliver them to the laboratory as quickly as possible. The number of samples to be tested depends
on the relevant regulation or quality assurance standard to be followed.
In order to prevent propagation or inactivation of contained microbes during transport to the laboratory
and subsequent storage, keep the sample at 5 °C ± 3 °C but never permitted to freeze.
Samples (i.e. composts and digestates) are liable to ferment and can contain pathogenic microorganisms.
It is essential to keep them away from any food or drink.
When transporting and handling samples, it is essential that national and international regulations
relating to bio-hazardous samples are followed.
4.3 General requirements for liquid materials
For safety reasons manual sampling is not recommended for liquid materials containing free ammonia.
Solutions, slurries and suspensions may be sampled manually provided the material is homogenized (see
Annex B for methods of mixing and associated precautions).
There is a risk that portions of multiphase liquids, sampled through narrow tubes or apertures, might not
be truly representative. Consequently, it is important to ensure that the internal dimensions of the
sampling devices are sufficiently large, i.e. in the region of 50 mm, to avoid this problem.
4.4 Moisture content
The moisture content shall subsequently be determined for solid material using the method specified in
1
EN 13040:— .
NOTE Material which has become excessively wet and which cannot be easily broken down into a flowable
material will not be suitable for the determination of quantity and cannot give a representative analytical result.
However, because of the diverse nature and bulk density of these materials, it is not possible to quantify what is
excessive. Examples are mushroom casing or blocking media that have become excessively moist, or material that
has become excessively wet in storage.

1
Under preparation. Stage at the time of publication: EN 10340:20xx.
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5 Apparatus
The sampling apparatus shall be clean, dry and made from materials which will not affect the
characteristics of the material to be sampled.
The special properties of liquid materials, including vapour pressure and stratification shall be taken into
account when choosing sampling apparatus.
5.1 Shovel, scoop or other sampling device so long as it preserves the characteristic of the material,
and is sterilizable for microbiological samples. Drills with a diameter of at least 3 times of the maximum
particle size may be used.
The release of material in a large batch of bulk material may be done by a wheel loader.
5.2 Apparatus for sample division, comprising any suitable equipment for combining and reducing
the samples which preserve the characteristic of the material.
5.3 Manual sampling devices for liquids, a weighted bottle or other vessel, capable of being lowered
into the material, sealed with a device to enable it to be opened at any specific depth.
A variant of this provides for gradual filling of the sample bottle as it is lowered from the surface of the
liquid to the base of its container. Typical devices are illustrated in Annex B within Figures B.1, B.2, B.3,
B.4 and B.5.
5.4 Sample valve on the storage vessel (illustrated in Annex B, Figure B.6).
5.5 Sample valve on a loading line out of the storage vessel (illustrated in Annex B, Figure B.7).
5.6 Sample valve on an external line through which material in storage is circulated (illustrated
in Annex B, Figure B.8).
5.7 Sample containers for the samples to be collected.
EXAMPLE Plastic bucket, plastic tub or plastic barrels in sufficient size.
5.8 Packing containers, air- and water-tight and with sufficient capacity.
5.9 Sterilizing device, to sterilize sampling devices where necessary.
6 Procedure for solid materials
6.1 General
In Annex D, Figure D.1, a schematic overview is given where the testing is carried out in one location from
the sampling procedure and the related handling of the sample at the laboratory. The individual steps are
explained in more detail in Clause 6 and Clause 7. The general scheme is applicable to liquid and solid
materials, either in bulk or in packed form. This scheme is not appropriate when a portion of a sample is
left at the sampling location. The sampling procedure depends on the laboratory determination to be
performed on the final sample.
Equal representative samples of one sampled portion can only be obtained by sample division of the
combined sample. This may be the case if different transportation and packaging requirements are
necessary for the analysis of different characteristics, or when chemical determinations on the sample
are carried out by multiple laboratories. Sample division cannot be performed on samples that are
collected for microbiological testing or bulk density. The minimal required volume of the final sample is
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given in Annex A. The stepwise process for sampling from bulk material and from packaged material is
illustrated in Annex E and Annex F respectively.
6.2 Location and time of sampling
From the sampled portion, calculate the number of incremental samples to be taken (see 6.4.1). The
sampling points shall be designated at random, this will ensure that they are taken throughout the
sampled portion.
Sampling of a sampled portion may be undertaken during loading and discharge.
Whenever possible, sampling from the bulk material shall be carried out from a moving stream of
material, the whole width of the stream being sampled.
6.3 Sampling constraints
6.3.1 Limitations on the sampled portion
If the consignment does not appear, either visually or from labelling, to be from the same batch (lot) or
consists of different materials then the materials shall be sampled separately.
NOTE Production coding can help in identifying the batch.
3
A sampled portion shall not be more than 5 000 m (bulk) or 10 000 packages (packaged material) of the
same material from the same consignment. If at all possible, packages which are damaged or adversely
affected by the environment shall not be selected as these may not give representative results (see also
NOTE to 4.4).
When sampling packages for quantity determination, each incremental sample shall be treated as a final
sample which shall be:
— either the individual package if it exceeds 30 l for material with particle size no greater than 60 mm;
— or the individual package if it exceeds 70 l for material with particle size greater than 60 mm;
— or sufficient packages to give a content of at least 30 l for material no greater than 60 mm, or 70 l for
material greater than 60 mm.
6.3.2 Number of final samples
Except for quantity determination and microbiological testing, and unless otherwise agreed with the
parties concerned, at least three
...

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