Water quality - Determination of total organic carbon (TOC), dissolved organic carbon (DOC), total bound nitrogen (TNb) and dissolved bound nitrogen (DNb) after high temperature catalytic oxidative combustion (ISO 20236:2018)

This International Standard specifies a method for the determination of total organic carbon (TOC), dissolved organic carbon (DOC), and for the determination of dissolved and particular bound nitrogen (TNb) in the form of free ammonia, ammonium, nitrite, nitrate and organic compounds capable of conversion to nitrogen oxides under the oxidative conditions described. The procedure is carried out instrumentally.
NOTE 1 Generally the method can be applied for the determination of total carbon (TC) and total inorganic carbon (TIC) (see Annex A in the Outline).
The method is applicable for water (e.g. drinking water, raw water, ground water, surface water, sea water or waste water) containing suspended material of ≤ 100 μm of particle size (convention). Reduce particles of > 100 μm of size to pieces of particle size of ≤ 100 μm before injection. The method allows a determination of TOC/DOC ≥ 1 mg/l C and TNb ≥ 1 mg/l N.
NOTE 2 The determination of carbon concentrations > 0,3 mg/l to 1 mg/l is only applicable in special cases, for example drinking water, measured by highly sensitive instruments. Cyanide, cyanate and particles of elemental carbon (soot), when present in the sample, can be determined together with the organic carbon. Volatile or purgeable organic carbon (VOC, POC) is not determined by this method. Dissolved nitrogen gas is not determined by this method. Generally, the working range is restricted by instrument dependant conditions (e.g. injection volume). Higher concentrations may be determined after appropriate dilution.

Wasserbeschaffenheit - Bestimmung des gesamten organischen Kohlenstoffs (TOC), des gelösten organischen Kohlenstoffs (DOC), des gebundenen Stickstoffs (TNb) und des gelösten gebundenen Stickstoffs (DNb) nach katalytischer oxidativer Hochtemperaturverbrennung (ISO 20236:2018)

Dieses Dokument legt ein Verfahren zur Bestimmung des gesamten organischen Kohlenstoffs (TOC), und des gelösten organischen Kohlenstoffs (DOC) fest sowie des gesamten gebundenen Stickstoffs (TNb) und des gelösten gebundenen Stickstoffs (DNb), der in Form von freiem Ammoniak, Ammonium, Nitrit, Nitrat vorliegt oder in organischen Verbindungen, die unter den beschriebenen Bedingungen in Stickstoffoxide umgewandelt werden können. Das Verfahren wird instrumentell durchgeführt.
ANMERKUNG   Grundsätzlich kann das Verfahren für die Bestimmung des Gesamtkohlenstoffs (TC) und des gesamten anorganischen Kohlenstoffs (TIC) angewendet werden (siehe Anhang A).
Das Verfahren ist anwendbar für Wasserproben (z. B. Trinkwasser, Rohwasser, Grundwasser, Oberflächen¬wasser, Meerwasser, Abwasser, Sickerwässer).
Das Verfahren erlaubt die Bestimmung von TOC und DOC ≥ 1 mg/l und von TNb und DNb ≥ 1 mg/l. Nach oben ist der Arbeitsbereich durch geräteabhängige Bedingungen (z. B. Injektionsvolumen) begrenzt. Höhere Konzentrationen können nach entsprechender Verdünnung der Probe bestimmt werden.
Bei Proben, die flüchtige organische Verbindungen enthalten (z. B. Industrieabwasser), wird das Differenzverfahren angewandt (siehe Anhang A).
Cyanid, Cyanat und Partikel aus elementarem Kohlenstoff (Ruß) können, falls in der Probe vorhanden, zusammen mit dem organischen Kohlenstoff erfasst werden.
Das Verfahren eignet sich nicht für die Bestimmung von bei den Bedingungen des Verfahrens flüchtigem oder austreibbarem organischem Kohlenstoff.
Gelöster, gasförmiger Stickstoff (N2) wird nicht erfasst.

Qualité de l'eau - Dosage du carbone organique total (COT), carbone organique (COD), azote lié total (TNb) et azote lié dissous (DNb) après combustion oxidatif catalytique à haute temperature (ISO 20236:2018)

Le présent document spécifie une méthode de dosage du carbone organique total (COT), du carbone organique dissous (COD), de l'azote lié total (TNb) et de l'azote lié dissous (DNb) sous la forme d'ammoniac libre, ammonium, nitrites, nitrates et composés organiques pouvant être convertis en oxydes d'azote dans les conditions décrites. La procédure est réalisée au moyen d'instruments.
NOTE            Généralement, cette méthode peut s'appliquer au dosage du carbone total (CT) et du carbone inorganique total (CIT), voir Annexe A.
Cette méthode s'applique aux échantillons d'eau (par exemple, eau destinée à la consommation humaine, eau brute, eau souterraine, eau de surface, eau de mer, eaux usées, lixiviats).
Cette méthode permet le dosage du COT et COD ≥ 1 mg/l et du TNb et DNb ≥ 1 mg/l. Le domaine d'analyse supérieur est restreint par les conditions liées aux instruments (par exemple, volume d'injection). Des concentrations supérieures peuvent être dosées après dilution adéquate de l'échantillon.
Pour les échantillons contenant des composés organiques volatils (par exemple, eaux résiduaires industrielles), la méthode par différence est utilisée, voir Annexe A.
Les cyanures, les cyanates et les particules de carbone élémentaire (suie), s'ils sont présents dans l'échantillon, peuvent être dosés avec le carbone organique.
Cette méthode ne convient pas au dosage du carbone organique volatil ou purgeable dans les conditions décrites par la présente méthode.
L'azote gazeux dissous (N2) n'est pas dosé.

Kakovost vode - Določevanje celotnega organskega ogljika (TOC), raztopljenega organskega ogljika (DOC), celotnega vezanega dušika (TNb) in raztopljenega vezanega dušika (DNb) po katalitskem sežigu pri visoki temperaturi (ISO 20236:2018)

Ta mednarodni standard določa metodo za določevanje celotnega organskega ogljika (TOC), raztopljenega organskega ogljika (DOC) ter za določevanje raztopljenega in posebno vezanega dušika (TNb) v obliki prostega amoniaka, amoniaka, nitrita, nitrata in organskih spojin, ki se lahko pod opisanimi oksidativnimi pogoji pretvorijo v dušikove okside. Postopek se izvaja instrumentalno.
OPOMBA 1: Metodo je v splošnem mogoče uporabiti za določevanje skupnega ogljika (TC) in skupnega anorganskega ogljika (TIC) (glej dodatek A v pregledu).
Metoda se uporablja za vodo (npr. pitno vodo, neobdelano vodo, podtalnico, površinsko vodo, morsko vodo ali odpadno vodo), ki vsebuje suspendiran material z velikostjo delcev ≤ 100 μm (dogovor). Pred vbrizgavanjem zmanjšajte delce velikosti > 100 μm na delce velikosti ≤ 100 μm. Metoda omogoča določevanje celotnega organskega ogljika in raztopljenega organskega ogljika ≥ 1 mg/l C ter raztopljenega in posebno vezanega dušika ≥ 1 mg/l N.
OPOMBA 2: Določitev koncentracij ogljika > 0,3 mg/l do 1 mg/l se uporablja samo v posebnih primerih (npr. pitna voda) pri merjenju z visoko občutljivi instrumenti. Cianid, cianat in delce elementarnega ogljika (saje), kadar so prisotni v vzorcu, je mogoče določiti skupaj z organskim ogljikom. Hlapni ali izprani organski ogljik (VOC, POC) ni določen s to metodo. Raztopljeni dušikov plin ni določen s to metodo. Na splošno je delovno območje omejeno s pogoji, ki so odvisni od instrumentov (npr. vbrizgana količina). Višje koncentracije se lahko določijo po ustreznem redčenju.

General Information

Status
Published
Public Enquiry End Date
01-Oct-2021
Publication Date
12-Dec-2021
Technical Committee
Current Stage
6060 - National Implementation/Publication (Adopted Project)
Start Date
08-Dec-2021
Due Date
12-Feb-2022
Completion Date
13-Dec-2021

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Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 20236:2022
01-januar-2022
Nadomešča:
SIST EN 12260:2003
Kakovost vode - Določevanje celotnega organskega ogljika (TOC), raztopljenega
organskega ogljika (DOC), celotnega vezanega dušika (TNb) in raztopljenega
vezanega dušika (DNb) po katalitskem sežigu pri visoki temperaturi (ISO
20236:2018)
Water quality - Determination of total organic carbon (TOC), dissolved organic carbon
(DOC), total bound nitrogen (TNb) and dissolved bound nitrogen (DNb) after high
temperature catalytic oxidative combustion (ISO 20236:2018)
Wasserbeschaffenheit - Bestimmung des gesamten organischen Kohlenstoffs (TOC),
des gelösten organischen Kohlenstoffs (DOC), des gebundenen Stickstoffs (TNb) und
des gelösten gebundenen Stickstoffs (DNb) nach katalytischer oxidativer
Hochtemperaturverbrennung (ISO 20236:2018)
Qualité de l'eau - Dosage du carbone organique total (COT), carbone organique (COD),
azote lié total (TNb) et azote lié dissous (DNb) après combustion oxidatif catalytique à
haute temperature (ISO 20236:2018)
Ta slovenski standard je istoveten z: EN ISO 20236:2021
ICS:
13.060.50 Preiskava vode na kemične Examination of water for
snovi chemical substances
SIST EN ISO 20236:2022 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 20236:2022

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SIST EN ISO 20236:2022


EN ISO 20236
EUROPEAN STANDARD

NORME EUROPÉENNE

November 2021
EUROPÄISCHE NORM
ICS 13.060.50 Supersedes EN 12260:2003
English Version

Water quality - Determination of total organic carbon
(TOC), dissolved organic carbon (DOC), total bound
nitrogen (TNb) and dissolved bound nitrogen (DNb) after
high temperature catalytic oxidative combustion (ISO
20236:2018)
Qualité de l'eau - Dosage du carbone organique total Wasserbeschaffenheit - Bestimmung des gesamten
(COT), carbone organique (COD), azote lié total (TNb) organischen Kohlenstoffs (TOC), des gelösten
et azote lié dissous (DNb) après combustion oxidatif organischen Kohlenstoffs (DOC), des gebundenen
catalytique à haute temperature (ISO 20236:2018) Stickstoffs (TNb) und des gelösten gebundenen
Stickstoffs (DNb) nach katalytischer oxidativer
Hochtemperaturverbrennung (ISO 20236:2018)
This European Standard was approved by CEN on 15 November 2021.

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. Up-to-date lists and bibliographical references
concerning such national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN
member.

This European Standard exists 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, Turkey and
United Kingdom.





EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION

EUROPÄISCHES KOMITEE FÜR NORMUNG

CEN-CENELEC Management Centre: Rue de la Science 23, B-1040 Brussels
© 2021 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 20236:2021 E
worldwide for CEN national Members.

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SIST EN ISO 20236:2022
EN ISO 20236:2021 (E)
Contents Page
European foreword . 3
Endorsement notice . 3

2

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SIST EN ISO 20236:2022
EN ISO 20236:2021 (E)
European foreword
The text of ISO 20236:2018 has been prepared by Technical Committee ISO/TC 147 "Water quality” of
the International Organization for Standardization (ISO) and has been taken over as EN ISO 20236:2021
by Technical Committee CEN/TC 230 “Water analysis” the secretariat of which is held by DIN.
This European Standard shall be given the status of a national standard, either by publication of an
identical text or by endorsement, at the latest by May 2022, and conflicting national standards shall be
withdrawn at the latest by May 2022.
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CEN shall not be held responsible for identifying any or all such patent rights.
This document supersedes EN 12260:2003.
Any feedback and questions on this document should be directed to the users’ national standards body.
A complete listing of these bodies can be found on the CEN website.
According to the CEN-CENELEC Internal Regulations, the national standards organizations of the
following countries are bound to implement this European Standard: 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, Turkey and the
United Kingdom.
Endorsement notice
The text of ISO 20236:2018 has been approved by CEN as EN ISO 20236:2021 without any modification.


3

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SIST EN ISO 20236:2022

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SIST EN ISO 20236:2022
INTERNATIONAL ISO
STANDARD 20236
First edition
2018-09
Water quality — Determination of
total organic carbon (TOC), dissolved
organic carbon (DOC), total bound
nitrogen (TN ) and dissolved bound
b
nitrogen (DN ) after high temperature
b
catalytic oxidative combustion
Qualité de l'eau — Dosage du carbone organique total (COT),
carbone organique (COD), azote lié total (TN ) et azote lié dissous
b
(DN ) après combustion oxidatif catalytique à haute temperature
b
Reference number
ISO 20236:2018(E)
©
ISO 2018

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SIST EN ISO 20236:2022
ISO 20236:2018(E)

COPYRIGHT PROTECTED DOCUMENT
© ISO 2018
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address
below or ISO’s member body in the country of the requester.
ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Fax: +41 22 749 09 47
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
ii © ISO 2018 – All rights reserved

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SIST EN ISO 20236:2022
ISO 20236:2018(E)

Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 1
4 Principle . 2
5 Interferences . 3
5.1 General . 3
5.2 TOC or DOC . . 3
5.3 TN or DN . 4
b b
6 Reagents . 4
7 Apparatus . 6
8 Quality requirements for the analytical system . 8
8.1 System check . 8
8.2 Recovery and variation of replicate determinations for particle processing control
for TOC and TN .8
b
9 Sampling and sample preparation . 8
10 Procedure. 9
10.1 General . 9
10.2 Calibration . 9
10.3 Validity check of the calibration function . 9
10.4 Measurement . 9
10.4.1 General. 9
10.4.2 Determination .10
11 Evaluation .11
12 Expression of results .11
13 Test report .11
Annex A (normative) Determination of TOC and TIC applying the difference method .12
Annex B (informative) Performance data for TOC or DOC and TN or DN .15
b b
Annex C (informative) Alternative detection techniques for TN and DN .17
b b
Bibliography .18
© ISO 2018 – All rights reserved iii

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SIST EN ISO 20236:2022
ISO 20236:2018(E)

Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards
bodies (ISO member bodies). The work of preparing International Standards is normally carried out
through ISO technical committees. Each member body interested in a subject for which a technical
committee has been established has the right to be represented on that committee. International
organizations, governmental and non-governmental, in liaison with ISO, also take part in the work.
ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of
electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are
described in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the
different types of ISO documents should be noted. This document was drafted in accordance with the
editorial rules of the ISO/IEC Directives, Part 2 (see www .iso .org/directives).
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. ISO shall not be held responsible for identifying any or all such patent rights. Details of
any patent rights identified during the development of the document will be in the Introduction and/or
on the ISO list of patent declarations received (see www .iso .org/patents).
Any trade name used in this document is information given for the convenience of users and does not
constitute an endorsement.
For an explanation of the voluntary nature of standards, the meaning of ISO specific terms and
expressions related to conformity assessment, as well as information about ISO’s adherence to the
World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT) see www .iso
.org/iso/foreword .html.
This document was prepared by Technical Committee ISO/TC 147, Water quality, Subcommittee SC 2,
Physical, chemical and biochemical methods.
Any feedback or questions on this document should be directed to the user’s national standards body. A
complete listing of these bodies can be found at www .iso .org/members .html.
iv © ISO 2018 – All rights reserved

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SIST EN ISO 20236:2022
ISO 20236:2018(E)

Introduction
Total organic carbon (TOC), dissolved organic carbon (DOC), total bound nitrogen (TN ) and dissolved
b
bound nitrogen (DN ) are an analytical convention, the respective result of which is a parameter used
b
for water quality control purposes. These parameters represent the sum of organically bound carbon
as well as the sum of inorganic and organic nitrogen (but not nitrogen gas), which can be dissolved in
water or bonded to dissolved or suspended matter under specified conditions and, if the sample is not
filtered, includes that associated with suspended matter. It does not give information on the nature of
the substances.
Details of an interlaboratory trial on the performance data for TOC or DOC and TN or DN are given in
b b
Annex B.
© ISO 2018 – All rights reserved v

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SIST EN ISO 20236:2022

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SIST EN ISO 20236:2022
INTERNATIONAL STANDARD ISO 20236:2018(E)
Water quality — Determination of total organic carbon
(TOC), dissolved organic carbon (DOC), total bound
nitrogen (TN ) and dissolved bound nitrogen (DN ) after
b b
high temperature catalytic oxidative combustion
WARNING — Persons using this document should be familiar with normal laboratory practice.
This document does not purport to address all of the safety problems, if any, associated with its
use. It is the responsibility of the user to establish appropriate safety and health practices.
IMPORTANT — It is absolutely essential that tests conducted in accordance with this document
be carried out by suitably qualified staff.
1 Scope
This document specifies a method for the determination of total organic carbon (TOC), dissolved
organic carbon (DOC), total bound nitrogen (TN ) and dissolved bound nitrogen (DN ) in the form of
b b
free ammonia, ammonium, nitrite, nitrate and organic compounds capable of conversion to nitrogen
oxides under the conditions described. The procedure is carried out instrumentally.
NOTE Generally the method can be applied for the determination of total carbon (TC) and total inorganic
carbon (TIC), see Annex A.
The method is applicable to water samples (e.g. drinking water, raw water, ground water, surface water,
sea water, waste water, leachates).
The method allows a determination of TOC and DOC ≥ 1 mg/l and TN and DN ≥ 1 mg/l. The upper
b b
working range is restricted by instrument-dependent conditions (e.g. injection volume). Higher
concentrations can be determined after appropriate dilution of the sample.
For samples containing volatile organic compounds (e.g. industrial waste water), the difference method
is used, see Annex A.
Cyanide, cyanate and particles of elemental carbon (soot), when present in the sample, can be
determined together with the organic carbon.
The method is not appropriate for the determination of volatile, or purgeable, organic carbon under the
conditions described by this method.
Dissolved nitrogen gas (N ) is not determined.
2
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.
ISO 8466-1, Water quality — Calibration and evaluation of analytical methods and estimation of
performance characteristics — Part 1: Statistical evaluation of the linear calibration function
3 Terms and definitions
For the purposes of this document, the following terms and definitions apply.
© ISO 2018 – All rights reserved 1

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SIST EN ISO 20236:2022
ISO 20236:2018(E)

ISO and IEC maintain terminological databases for use in standardization at the following addresses:
— ISO Online browsing platform: available at https: //www .iso .org ./obp
— IEC Electropedia: available at https: //www .electropedia .org/
3.1
total carbon
TC
sum of organically and inorganically bound carbon present in water, including elemental carbon
3.2
total inorganic carbon
TIC
sum of inorganic carbon present in water sample measured under the conditions of this method
Note 1 to entry: TIC is measured as CO originating only from carbonates, hydrogen carbonates and dissolved
2
carbon dioxide.
3.3
total organic carbon
TOC
sum of organically bound carbon present in water, bonded to dissolved or suspended matter, including
cyanate, thiocyanate and elemental carbon measured under the conditions of this method
Note 1 to entry: Volatile organic carbon cannot be guaranteed to be determined by the method.
Note 2 to entry: Generally, TOC includes organic compounds in water that cannot be purged under the conditions
of this method, also known as non-purgeable organic carbon (NPOC).
3.4
dissolved organic carbon
DOC
sum of organically bound carbon present in water originating from compounds passing through a
membrane filter of 0,45 µm pore size, including cyanate and thiocyanate measured under the conditions
of this method
3.5
total bound nitrogen
TN
b
sum of organically bound and inorganically bound nitrogen present in water or suspended matter
measured under the conditions of this method
3.6
dissolved bound nitrogen
DN
b
sum of organically and inorganically bound nitrogen present in water originating from compounds
passing through a 0,45 µm membrane filter measured under the conditions of this method
4 Principle
Thermal catalytic combustion of the sample containing organic carbon, and inorganic and organic
nitrogen in an oxygen-containing atmosphere at ≥ 680 °C for TOC or DOC and ≥ 720 °C for TN or DN
b b
determinations.
The TOC or DOC determination is carried out in accordance with the direct measurement method.
2 © ISO 2018 – All rights reserved

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SIST EN ISO 20236:2022
ISO 20236:2018(E)

Prior to combustion, remove inorganic carbon by acidification and purging with a carrier gas (6.7).
NOTE Platinum and cerium(IV), for example, can be used as catalyst material for combustion. The catalyst
serves to accelerate the oxidation process of carbon containing water constituents in excess of oxygen to
produce the required carbon dioxide gas for the detection process. Depending on combustion temperature
and temperatures in the combustion zone, different catalysts can be used, e.g. metals or metal oxides for
temperatures > 680 °C or sintered Alumina for temperatures around 1 200 °C, according to verifications of
different suppliers.
Oxidation of organic carbon (TOC, DOC) with oxygen or synthetic air to carbon dioxide. Detection by
means of infrared spectrometry (IR). Combustion of inorganic and organic nitrogen with oxygen or
synthetic air and conversion to nitric oxide.
Reaction with ozone giving electronically excited nitrogen oxides. Detection by means of
chemiluminescence (CLD) (see Annex C for alternative detection).
This document can be applied for the determination of TOC or DOC and TN or DN separately or for
b b
simultaneous TOC or DOC and TN or DN determinations, for example connecting the IR detector with
b b
a CLD in series.
Quality control is necessary to check the validity of the calibration function (see 10.3). Replicate
determinations can be necessary. The method of standard addition can be required if matrix
interferences are expected (see 5.3 and 10.4.2.1).
5 Interferences
5.1 General
Interferences with the determination of TOC or DOC and TN or DN can arise from memory effects.
b b
Replicate injections are necessary (see 10.4.1).
Detergents, oils and fats can influence the surface tension of the sample, causing erroneous data. A
dilution of the sample can reduce such risk.
Samples with extreme pH values, highly buffered samples and samples with high salt contents can
cause interference. Seek advice from the manufacturer to solve these interferences.
Suspended material can lead to a loss of quality of the analytical result. If a homogenized sample
containing suspended material produces results obtained from replicate measurements that deviate by
more than 10 %, an accurate TOC or TN result cannot be obtained on the sample.
b
5.2 TOC or DOC
Inorganic carbon (e.g. CO or ions of carbonic acid) present in the sample interferes with the
2
determination of TOC or DOC. Inorganic carbon is removed by acidification and purging with a gas
that is free from CO and organic compounds prior to the TOC or DOC determination (see 10.4.2.2 and
2
10.4.2.3).
NOTE 1 Alternatively, the differential method determining the TC and TIC separately can be applied
(see Annex A). The TOC can be calculated by subtracting TIC from the TC. This calculation leads to correct results
only as long as carbon monoxide, cyanide, cyanate and thiocyanate are present with negligible concentrations.
NOTE 2 Purgeable organic carbon substances, such as benzene, toluene, cyclohexane and chloroform,
can partly escape upon stripping (see 10.4.2.2 and 10.4.2.3). In the presence of these substances, the TOC
concentration can be determined separately, for example by applying the differential method (see Annex A).
© ISO 2018 – All rights reserved 3

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SIST EN ISO 20236:2022
ISO 20236:2018(E)

5.3 TN or DN
b b
High loads of dissolved or total organic carbon (DOC or TOC) can lead to poor recovery of TN or DN .
b b
Suspected problems can be identified by determining nitrogen before and after suitable dilution, or by
using standard addition techniques.
Not all organic nitrogen compounds are quantitatively converted to nitrogen oxide by the combustion
procedure described, and consequently to nitrogen dioxide by the reaction with ozone. Poor recoveries
can occur with compounds containing either double- or triple-bonded nitrogen atoms. The use of
a calibration function calculated in accordance with 10.2 and applying a nitrogen mixed standard
solution II (6.9.3.4) can result in a negative TN bias for ammonium-N determinations (e.g. ammonium
b
sulfate solution) and a positive bias for nitrate-N determinations (e.g. potassium nitrate solution).
6 Reagents
Use reagents of pro analysis grade, if available.
Dry all solid reagents for at least 1 h at (105 ± 5) °C. Store the dried solid in a desiccator before weighing.
NOTE It is not necessary to dry cellulose before usage.
Prepare alternative concentrations and volumes of solutions as described hereafter, if necessary.
Alternatively, use commercially available stock solutions of the required concentration.
When applying the simultaneous determination of TN and TOC, an appropriate mixture of the
b
1 000 mg/l TOC and TN stock solutions (6.8.2 and 6.9.3.3) for the preparation of standard and
b
calibration solutions can be used.
6.1 Water.
The contents of carbon and bound nitrogen in water used for the preparation of samples and solutions
shall be sufficiently low to be negligible in comparison with the lowest TOC and TN concentration to
b
be determined.
6.2 Sulfuric acid, ρ = 1,84 g/ml.
6.3 Hydrochloric acid, ω(HCl) = 32 %.
6.4 Nicotinic acid, C H NO , > 99,5 %.
6 5 2
6.5 TOC and TN stock solution for system check.
b
Place 8,793 g of nicotinic acid (6.4) in a 1 000 ml volumetric flask. Dissolve and dilute to volume with
water (6.1).
The solution contains 5 147 mg/l of carbon and 1 000 mg/l of nitrogen.
The solution is stable for six months if stored at (3 ± 2) °C.
6.6 Blank solution.
Fill a 100 ml volumetric flask with water (6.1).
6.7 Gases or synthetic air, free from impurities with influence of the determinant (e.g. carbon dioxide,
organic carbon, nitrogen compounds).
Use gases in accordance with the manufacturer’s specifications, for example oxygen, 99,7 % volume
fraction.
4 © ISO 2018 – All rights reserved

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SIST EN ISO 20236:2022
ISO 20236:2018(E)

6.8 Reagents for the TOC or DOC determination.
6.8.1 Potassium hydrogen phthalate, C H KO .
8 5 4
6.8.2 Potassium hydrogen phthalate stock solution, ρ(C) = 1 000 mg/l.
Place 2,125 g of potassium hydrogen phthalate (6.8.1) in a 1 000 ml volumetric flask. Dissolve and dilute
to volume with water (6.1).
The solution is stable for six months if stored at (3 ± 2) °C.
6.8.3 Potassium hydrogen phthalate standard solution, ρ(C) = 100 mg/l.
Pipette 100 ml of the potassium hydrogen phthalate stock standard solution (6.8.2) into a 1 000 ml
volumetric flask and dilute to volume with water (6.1).
The solution is stable for one month if stored at (3 ± 2) °C.
6.8.4 TOC and DOC calibration solutions.
Depending on the TOC or DOC concentration expected in the sample, use the potassium hydrogen
phthalate standard solution (6.8.3) to prepare five to ten calibration solutions distributed over the
expected working range as evenly as possible.
For example, proceed as follows for the range 1,0 mg/l C to 10 mg/l C.
Pipette the following volumes into a series of 100 ml volumetric flasks: 1,0 ml, 2,0 ml, 3,0 ml, 4,0 ml,
5,0 ml, 6,0 ml, 7,0 ml, 8,0 ml, 9,0 ml or 10,0 ml of the potassium hydrogen phthalate standard solution
(6.8.3) and dilute to volume with water (6.1).
The concentrations of carbon in these calibration solutions are: 1 mg/l, 2 mg/l, 3 mg/l, 4 mg/l, 5 mg/l,
6 mg/l, 7 mg/l, 8 mg/l, 9 mg/l or 10 mg/l, respectively.
Prepare the calibration solutions on the day of use.
6.8.5 Hydrochloric acid TIC stripping solution, c(HCl) = e.g. 3 mol/l.
6.8.6 Cellulose, (C H O ) , microcrystalline, of partic
...

SLOVENSKI STANDARD
oSIST prEN ISO 20236:2021
01-september-2021
Kakovost vode - Določevanje celotnega organskega ogljika (TOC), raztopljenega
organskega ogljika (DOC), celotnega vezanega dušika (TNb) in raztopljenega
vezanega dušika (DNb) po katalitskem sežigu pri visoki temperaturi (ISO
20236:2018)
Water quality - Determination of total organic carbon (TOC), dissolved organic carbon
(DOC), total bound nitrogen (TNb) and dissolved bound nitrogen (DNb) after high
temperature catalytic oxidative combustion (ISO 20236:2018)
Wasserbeschaffenheit - Bestimmung des gesamten organischen Kohlenstoffs (TOC),
des gelösten organischen Kohlenstoffs (DOC), des gebundenen Stickstoffs (TNb) und
des gelösten gebundenen Stickstoffs (DNb) nach katalytischer oxidativer
Hochtemperaturverbrennung (ISO 20236:2018)
Qualité de l'eau - Dosage du carbone organique total (COT), carbone organique (COD),
azote lié total (TNb) et azote lié dissous (DNb) après combustion oxidatif catalytique à
haute temperature (ISO 20236:2018)
Ta slovenski standard je istoveten z: prEN ISO 20236
ICS:
13.060.50 Preiskava vode na kemične Examination of water for
snovi chemical substances
oSIST prEN ISO 20236:2021 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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oSIST prEN ISO 20236:2021

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oSIST prEN ISO 20236:2021
INTERNATIONAL ISO
STANDARD 20236
First edition
2018-09
Water quality — Determination of
total organic carbon (TOC), dissolved
organic carbon (DOC), total bound
nitrogen (TN ) and dissolved bound
b
nitrogen (DN ) after high temperature
b
catalytic oxidative combustion
Qualité de l'eau — Dosage du carbone organique total (COT),
carbone organique (COD), azote lié total (TN ) et azote lié dissous
b
(DN ) après combustion oxidatif catalytique à haute temperature
b
Reference number
ISO 20236:2018(E)
©
ISO 2018

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oSIST prEN ISO 20236:2021
ISO 20236:2018(E)

COPYRIGHT PROTECTED DOCUMENT
© ISO 2018
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address
below or ISO’s member body in the country of the requester.
ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Fax: +41 22 749 09 47
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
ii © ISO 2018 – All rights reserved

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oSIST prEN ISO 20236:2021
ISO 20236:2018(E)

Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 1
4 Principle . 2
5 Interferences . 3
5.1 General . 3
5.2 TOC or DOC . . 3
5.3 TN or DN . 4
b b
6 Reagents . 4
7 Apparatus . 6
8 Quality requirements for the analytical system . 8
8.1 System check . 8
8.2 Recovery and variation of replicate determinations for particle processing control
for TOC and TN .8
b
9 Sampling and sample preparation . 8
10 Procedure. 9
10.1 General . 9
10.2 Calibration . 9
10.3 Validity check of the calibration function . 9
10.4 Measurement . 9
10.4.1 General. 9
10.4.2 Determination .10
11 Evaluation .11
12 Expression of results .11
13 Test report .11
Annex A (normative) Determination of TOC and TIC applying the difference method .12
Annex B (informative) Performance data for TOC or DOC and TN or DN .15
b b
Annex C (informative) Alternative detection techniques for TN and DN .17
b b
Bibliography .18
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Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards
bodies (ISO member bodies). The work of preparing International Standards is normally carried out
through ISO technical committees. Each member body interested in a subject for which a technical
committee has been established has the right to be represented on that committee. International
organizations, governmental and non-governmental, in liaison with ISO, also take part in the work.
ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of
electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are
described in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the
different types of ISO documents should be noted. This document was drafted in accordance with the
editorial rules of the ISO/IEC Directives, Part 2 (see www .iso .org/directives).
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. ISO shall not be held responsible for identifying any or all such patent rights. Details of
any patent rights identified during the development of the document will be in the Introduction and/or
on the ISO list of patent declarations received (see www .iso .org/patents).
Any trade name used in this document is information given for the convenience of users and does not
constitute an endorsement.
For an explanation of the voluntary nature of standards, the meaning of ISO specific terms and
expressions related to conformity assessment, as well as information about ISO’s adherence to the
World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT) see www .iso
.org/iso/foreword .html.
This document was prepared by Technical Committee ISO/TC 147, Water quality, Subcommittee SC 2,
Physical, chemical and biochemical methods.
Any feedback or questions on this document should be directed to the user’s national standards body. A
complete listing of these bodies can be found at www .iso .org/members .html.
iv © ISO 2018 – All rights reserved

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oSIST prEN ISO 20236:2021
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Introduction
Total organic carbon (TOC), dissolved organic carbon (DOC), total bound nitrogen (TN ) and dissolved
b
bound nitrogen (DN ) are an analytical convention, the respective result of which is a parameter used
b
for water quality control purposes. These parameters represent the sum of organically bound carbon
as well as the sum of inorganic and organic nitrogen (but not nitrogen gas), which can be dissolved in
water or bonded to dissolved or suspended matter under specified conditions and, if the sample is not
filtered, includes that associated with suspended matter. It does not give information on the nature of
the substances.
Details of an interlaboratory trial on the performance data for TOC or DOC and TN or DN are given in
b b
Annex B.
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oSIST prEN ISO 20236:2021
INTERNATIONAL STANDARD ISO 20236:2018(E)
Water quality — Determination of total organic carbon
(TOC), dissolved organic carbon (DOC), total bound
nitrogen (TN ) and dissolved bound nitrogen (DN ) after
b b
high temperature catalytic oxidative combustion
WARNING — Persons using this document should be familiar with normal laboratory practice.
This document does not purport to address all of the safety problems, if any, associated with its
use. It is the responsibility of the user to establish appropriate safety and health practices.
IMPORTANT — It is absolutely essential that tests conducted in accordance with this document
be carried out by suitably qualified staff.
1 Scope
This document specifies a method for the determination of total organic carbon (TOC), dissolved
organic carbon (DOC), total bound nitrogen (TN ) and dissolved bound nitrogen (DN ) in the form of
b b
free ammonia, ammonium, nitrite, nitrate and organic compounds capable of conversion to nitrogen
oxides under the conditions described. The procedure is carried out instrumentally.
NOTE Generally the method can be applied for the determination of total carbon (TC) and total inorganic
carbon (TIC), see Annex A.
The method is applicable to water samples (e.g. drinking water, raw water, ground water, surface water,
sea water, waste water, leachates).
The method allows a determination of TOC and DOC ≥ 1 mg/l and TN and DN ≥ 1 mg/l. The upper
b b
working range is restricted by instrument-dependent conditions (e.g. injection volume). Higher
concentrations can be determined after appropriate dilution of the sample.
For samples containing volatile organic compounds (e.g. industrial waste water), the difference method
is used, see Annex A.
Cyanide, cyanate and particles of elemental carbon (soot), when present in the sample, can be
determined together with the organic carbon.
The method is not appropriate for the determination of volatile, or purgeable, organic carbon under the
conditions described by this method.
Dissolved nitrogen gas (N ) is not determined.
2
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.
ISO 8466-1, Water quality — Calibration and evaluation of analytical methods and estimation of
performance characteristics — Part 1: Statistical evaluation of the linear calibration function
3 Terms and definitions
For the purposes of this document, the following terms and definitions apply.
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ISO 20236:2018(E)

ISO and IEC maintain terminological databases for use in standardization at the following addresses:
— ISO Online browsing platform: available at https: //www .iso .org ./obp
— IEC Electropedia: available at https: //www .electropedia .org/
3.1
total carbon
TC
sum of organically and inorganically bound carbon present in water, including elemental carbon
3.2
total inorganic carbon
TIC
sum of inorganic carbon present in water sample measured under the conditions of this method
Note 1 to entry: TIC is measured as CO originating only from carbonates, hydrogen carbonates and dissolved
2
carbon dioxide.
3.3
total organic carbon
TOC
sum of organically bound carbon present in water, bonded to dissolved or suspended matter, including
cyanate, thiocyanate and elemental carbon measured under the conditions of this method
Note 1 to entry: Volatile organic carbon cannot be guaranteed to be determined by the method.
Note 2 to entry: Generally, TOC includes organic compounds in water that cannot be purged under the conditions
of this method, also known as non-purgeable organic carbon (NPOC).
3.4
dissolved organic carbon
DOC
sum of organically bound carbon present in water originating from compounds passing through a
membrane filter of 0,45 µm pore size, including cyanate and thiocyanate measured under the conditions
of this method
3.5
total bound nitrogen
TN
b
sum of organically bound and inorganically bound nitrogen present in water or suspended matter
measured under the conditions of this method
3.6
dissolved bound nitrogen
DN
b
sum of organically and inorganically bound nitrogen present in water originating from compounds
passing through a 0,45 µm membrane filter measured under the conditions of this method
4 Principle
Thermal catalytic combustion of the sample containing organic carbon, and inorganic and organic
nitrogen in an oxygen-containing atmosphere at ≥ 680 °C for TOC or DOC and ≥ 720 °C for TN or DN
b b
determinations.
The TOC or DOC determination is carried out in accordance with the direct measurement method.
2 © ISO 2018 – All rights reserved

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Prior to combustion, remove inorganic carbon by acidification and purging with a carrier gas (6.7).
NOTE Platinum and cerium(IV), for example, can be used as catalyst material for combustion. The catalyst
serves to accelerate the oxidation process of carbon containing water constituents in excess of oxygen to
produce the required carbon dioxide gas for the detection process. Depending on combustion temperature
and temperatures in the combustion zone, different catalysts can be used, e.g. metals or metal oxides for
temperatures > 680 °C or sintered Alumina for temperatures around 1 200 °C, according to verifications of
different suppliers.
Oxidation of organic carbon (TOC, DOC) with oxygen or synthetic air to carbon dioxide. Detection by
means of infrared spectrometry (IR). Combustion of inorganic and organic nitrogen with oxygen or
synthetic air and conversion to nitric oxide.
Reaction with ozone giving electronically excited nitrogen oxides. Detection by means of
chemiluminescence (CLD) (see Annex C for alternative detection).
This document can be applied for the determination of TOC or DOC and TN or DN separately or for
b b
simultaneous TOC or DOC and TN or DN determinations, for example connecting the IR detector with
b b
a CLD in series.
Quality control is necessary to check the validity of the calibration function (see 10.3). Replicate
determinations can be necessary. The method of standard addition can be required if matrix
interferences are expected (see 5.3 and 10.4.2.1).
5 Interferences
5.1 General
Interferences with the determination of TOC or DOC and TN or DN can arise from memory effects.
b b
Replicate injections are necessary (see 10.4.1).
Detergents, oils and fats can influence the surface tension of the sample, causing erroneous data. A
dilution of the sample can reduce such risk.
Samples with extreme pH values, highly buffered samples and samples with high salt contents can
cause interference. Seek advice from the manufacturer to solve these interferences.
Suspended material can lead to a loss of quality of the analytical result. If a homogenized sample
containing suspended material produces results obtained from replicate measurements that deviate by
more than 10 %, an accurate TOC or TN result cannot be obtained on the sample.
b
5.2 TOC or DOC
Inorganic carbon (e.g. CO or ions of carbonic acid) present in the sample interferes with the
2
determination of TOC or DOC. Inorganic carbon is removed by acidification and purging with a gas
that is free from CO and organic compounds prior to the TOC or DOC determination (see 10.4.2.2 and
2
10.4.2.3).
NOTE 1 Alternatively, the differential method determining the TC and TIC separately can be applied
(see Annex A). The TOC can be calculated by subtracting TIC from the TC. This calculation leads to correct results
only as long as carbon monoxide, cyanide, cyanate and thiocyanate are present with negligible concentrations.
NOTE 2 Purgeable organic carbon substances, such as benzene, toluene, cyclohexane and chloroform,
can partly escape upon stripping (see 10.4.2.2 and 10.4.2.3). In the presence of these substances, the TOC
concentration can be determined separately, for example by applying the differential method (see Annex A).
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5.3 TN or DN
b b
High loads of dissolved or total organic carbon (DOC or TOC) can lead to poor recovery of TN or DN .
b b
Suspected problems can be identified by determining nitrogen before and after suitable dilution, or by
using standard addition techniques.
Not all organic nitrogen compounds are quantitatively converted to nitrogen oxide by the combustion
procedure described, and consequently to nitrogen dioxide by the reaction with ozone. Poor recoveries
can occur with compounds containing either double- or triple-bonded nitrogen atoms. The use of
a calibration function calculated in accordance with 10.2 and applying a nitrogen mixed standard
solution II (6.9.3.4) can result in a negative TN bias for ammonium-N determinations (e.g. ammonium
b
sulfate solution) and a positive bias for nitrate-N determinations (e.g. potassium nitrate solution).
6 Reagents
Use reagents of pro analysis grade, if available.
Dry all solid reagents for at least 1 h at (105 ± 5) °C. Store the dried solid in a desiccator before weighing.
NOTE It is not necessary to dry cellulose before usage.
Prepare alternative concentrations and volumes of solutions as described hereafter, if necessary.
Alternatively, use commercially available stock solutions of the required concentration.
When applying the simultaneous determination of TN and TOC, an appropriate mixture of the
b
1 000 mg/l TOC and TN stock solutions (6.8.2 and 6.9.3.3) for the preparation of standard and
b
calibration solutions can be used.
6.1 Water.
The contents of carbon and bound nitrogen in water used for the preparation of samples and solutions
shall be sufficiently low to be negligible in comparison with the lowest TOC and TN concentration to
b
be determined.
6.2 Sulfuric acid, ρ = 1,84 g/ml.
6.3 Hydrochloric acid, ω(HCl) = 32 %.
6.4 Nicotinic acid, C H NO , > 99,5 %.
6 5 2
6.5 TOC and TN stock solution for system check.
b
Place 8,793 g of nicotinic acid (6.4) in a 1 000 ml volumetric flask. Dissolve and dilute to volume with
water (6.1).
The solution contains 5 147 mg/l of carbon and 1 000 mg/l of nitrogen.
The solution is stable for six months if stored at (3 ± 2) °C.
6.6 Blank solution.
Fill a 100 ml volumetric flask with water (6.1).
6.7 Gases or synthetic air, free from impurities with influence of the determinant (e.g. carbon dioxide,
organic carbon, nitrogen compounds).
Use gases in accordance with the manufacturer’s specifications, for example oxygen, 99,7 % volume
fraction.
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6.8 Reagents for the TOC or DOC determination.
6.8.1 Potassium hydrogen phthalate, C H KO .
8 5 4
6.8.2 Potassium hydrogen phthalate stock solution, ρ(C) = 1 000 mg/l.
Place 2,125 g of potassium hydrogen phthalate (6.8.1) in a 1 000 ml volumetric flask. Dissolve and dilute
to volume with water (6.1).
The solution is stable for six months if stored at (3 ± 2) °C.
6.8.3 Potassium hydrogen phthalate standard solution, ρ(C) = 100 mg/l.
Pipette 100 ml of the potassium hydrogen phthalate stock standard solution (6.8.2) into a 1 000 ml
volumetric flask and dilute to volume with water (6.1).
The solution is stable for one month if stored at (3 ± 2) °C.
6.8.4 TOC and DOC calibration solutions.
Depending on the TOC or DOC concentration expected in the sample, use the potassium hydrogen
phthalate standard solution (6.8.3) to prepare five to ten calibration solutions distributed over the
expected working range as evenly as possible.
For example, proceed as follows for the range 1,0 mg/l C to 10 mg/l C.
Pipette the following volumes into a series of 100 ml volumetric flasks: 1,0 ml, 2,0 ml, 3,0 ml, 4,0 ml,
5,0 ml, 6,0 ml, 7,0 ml, 8,0 ml, 9,0 ml or 10,0 ml of the potassium hydrogen phthalate standard solution
(6.8.3) and dilute to volume with water (6.1).
The concentrations of carbon in these calibration solutions are: 1 mg/l, 2 mg/l, 3 mg/l, 4 mg/l, 5 mg/l,
6 mg/l, 7 mg/l, 8 mg/l, 9 mg/l or 10 mg/l, respectively.
Prepare the calibration solutions on the day of use.
6.8.5 Hydrochloric acid TIC stripping solution, c(HCl) = e.g. 3 mol/l.
6.8.6 Cellulose, (C H O ) , microcrystalline, of particle size ranging from 0,02 mm to 0,1 mm.
6 10 5 n
6.8.6.1 Cellulose test suspension for particle processing control, ρ(C) = 100 mg/l.
Place 225 mg of cellulose (6.8.6) in a 1 000 ml volumetric flask, moist with water (6.1), and dilute to
volume with water (6.1).
The mixture is stable for one month if stored at (3 ± 2) °C.
Homogenize the suspension with a magnetic stirrer until the suspension is homogeneous before use.
Ultrasonic treatment should not be used because it reduces the particle size.
6.9 Reagents for the TN and DN determination.
b b
6.9.1 Ammonium sulfate, (NH ) SO .
4 2 4
6.9.2 Potassium nitrate, KNO .
3
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6.9.3 Nitrogen stock standard solutions.
6.9.3.1 Ammonium sulfate stock solution, ρ(N) = 1 000 mg/l.
Place 4,717 g of ammonium sulfate (6.9.1) in a 1 000 ml volumetric flask. Dissolve in 500 ml of water
(6.1) and dilute to volume with water (6.1).
The solution is stable for six months if stored at (3 ± 2) °C.
6.9.3.2 Potassium nitrate stock solution, ρ(N) = 1 000 mg/l.
Place 7,219 g of potassium nitrate (6.9.2) in a 1 000 ml volumetric flask. Dissolve and dilute to volume
with water (6.1).
The solution is stable for six months if stored at (3 ± 2) °C.
6.9.3.3 Nitrogen mixed standard solution I, ρ(N) = 1 000 mg/l.
Mix equal volumes of the solutions 6.9.3.1 and 6.9.3.2 to produce a nitrogen mixed standard solution.
The solution is stable for one month if stored at (3 ± 2) °C.
6.9.3.4 Nitrogen standard solution II, ρ(N) = 100 mg/l.
Pipette 100 ml of nitrogen mixed standard solution I (6.9.3.3) into a 1 000 ml volumetric flask, and
dilute to volume with water (6.1).
The solution is stable for one month if stored at (3 ± 2) °C.
6.9.4 TN and DN calibration solutions.
b b
Depending on the nitrogen concentration expected in the sample, use the nitrogen standard solution II
(6.9.3.4) to prepare five to ten calibration solutions distributed over the expected working range as
evenly as possible.
For example, proceed as follows for the range 1,0 mg/l to 10 mg/l N.
Pipette the following volumes into a series of 100 ml volumetric flasks: 1,0 ml, 2,0 ml, 3,0 ml, 4,0 ml,
5,0 ml, 6,0 ml, 7,0 ml, 8,0 ml, 9,0 ml or 10,0 ml of the nitrogen mixed standard solution II (6.9.3.4) and
dilute to volume with water (6.1).
The concentrations of nitrogen in these calibration solutions are: 1 mg/l, 2 mg/l, 3 mg/l, 4 mg/l, 5 mg/l,
6 mg/l, 7 mg/l, 8 mg/l, 9 mg/l or 10 mg/l, respectively.
Prepare the calibration solutions on the day of use.
7 Apparatus
The usual laboratory apparatus and, in particular, the following.
7.1 Homogenization and particle size reducing device, for the homogenization of dispersed matter,
for example a suitable ultrasonic apparatus or a rotor-stator homogenizer (see Clause 9), if needed.
NOTE An ultrasonic device is suitable for the homogenization of samples, but it is not suitable for the
homogenization of the cellulose test suspension (6.8.6.1) for particle processing control.
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ISO 20236:2018(E)

7.2 High temperature combustion system, see Figure 1, conforming to the quality requirements
given in Clause 8.
When measuring water samples containing particulate material, the instrument shall be capable of
injecting the particulate material.
NOTE Users applying a system for the simultaneous determination of TOC and TN can check for particle
b
procession using the TOC cellulose test suspension (6.8.6.1). No recommendation can be given for a suitable TN
b
test suspension.
In general, it shall consist of the following components.
7.2.1 Sample injection device, for automated or manual operation.
The use of an autosampler shall include a device to keep heterogeneous samples in a homogenous state
(e.g. magnetic stirrer) before injection.
7.2.2 Reaction vessel
Oven, heatable to at least to 680 °C for TOC or DOC and to 720 °C for TN or DN determinations.
b b
7.2.3 Detector.
7.2.3.1 IR detector for TOC or DOC.
7.2.3.2 Chemiluminescence detector (CLD) for TN or DN .
b b
NOTE See Annex C for alternative detectors.
7.2.4 Recording device, e.g. PC with software for data acquisition and evaluation.
Figure 1 — Examples for high temperature combustion system configurations with detectors
for the determination of A: TOC or DOC, B: DN or TN and C: TOC or DOC and DN and TN
b b b b
© ISO 2018 – All rights reserved 7

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8 Quality requirements for the analyt
...

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