This document specifies a method for determination of the drainability of water from a pulp suspension in terms of the “Canadian Standard” freeness method in millilitres. In principle, this method is applicable to all kinds of pulp in aqueous suspension. NOTE Treatments of pulp suspensions which produce a large proportion of fines can induce an anomalous rise in freeness (false freeness), as a rule at values below 100 ml.

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This document specifies a basic laboratory test method for deinkability of woodfree printed paper products as a mixture under alkaline conditions by means of single stage flotation deinking and fatty acid-based collector chemistry. The woodfree printed paper product of interest is tested as a mixture containing 10 % by weight of the woodfree printed paper with the balance comprising a mixture of printed wood-containing paper.

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This document describes the thermal analysis of kraft lignin using thermogravimetric methods. Thermogravimetry can be used to determine the initial decomposition temperature(s), rate(s) of decomposition, and the temperature at maximum decomposition of various materials, including lignins at atmospheric pressure. All these temperatures are solely based on the mass loss and are not necessarily the real decomposition temperatures, because not all decompositions can generate evaporation at atmospheric pressure. Thus, these values are only for comparison purposes. This procedure is applicable to solid lignins (e.g., powdered form) isolated using different isolation techniques (e.g., acidification with hydrochloric acid, sulphuric acid, etc., and carbonation using gaseous carbon dioxide) from the spent liquor (black liquor) generated in the kraft pulping process. It does not apply to raw black liquor. Thermogravimetric measurement may be performed under different types of atmosphere, e.g., an inert atmosphere or an oxidative atmosphere.

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This document describes a method for the determination of the glass transition temperature (Tg) of kraft lignin. The procedure utilizes differential scanning calorimetry (DSC). This procedure is applicable to solid lignins (e.g., powdered form) isolated using different isolation techniques (e.g., acidification with hydrochloric acid, sulfuric acid, etc., and carbonation using gaseous carbon dioxide) from the spent liquor (black liquor) generated from the kraft pulping process. It does not apply to raw black liquor and lignin in the alkali form, (lignin that is separated from wood chips and dissolved in sodium sulfide and sodium hydroxide liquor such as that originating from black liquor).

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This document specifies a method for the determination of stickies and non-tacky polymeric contaminants present in pulp or paper sheets near-infrared measurement. This document is applicable to recycled pulps and papers. Sampling of pulp and paper as well as the preparation of handsheets are outside the scope of this document.

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This document describes the general procedure for measuring the diffuse radiance factor of all types of pulp, paper and board. More particularly, it specifies in detail the procedures to be used for calibrating the equipment, and in Annex A, the characteristics of the equipment to be used for such measurements. This document can be used to measure the diffuse radiance factors and related properties of materials containing fluorescent whitening agents, provided that the UV-content of the instrument illumination has been adjusted to give the same level of fluorescence as a fluorescent reference standard for a selected CIE illuminant, according to the International Standard describing the measurement of the property in question. Annex C describes the preparation of fluorescent reference standards.

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This document describes methods for the determination of the dry matter content of lignins by oven-drying and freeze-drying. The methods are applicable to all types of lignins isolated from kraft, organosolv, soda, and sulfite pulping processes, and to lignin obtained by enzymatic or acid hydrolysis of biomass. However, the oven-drying method is not applicable to kraft lignins in the base form, also referred to as sodium form. Both methods are applicable only to lignins in the solid form.

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This method describes procedures for the determination of inorganics content in kraft, soda, and hydrolysis lignin. The method is applicable to lignin isolated from a kraft pulping process, a soda pulping process, or lignin obtained by hydrolysis of biomass. For kraft lignin in the acid form, soda lignin, and hydrolysis lignin, the inorganics content is determined from the ash content of the sample. For kraft lignin in the base form, the inorganics content is determined from the sum of the contents of calcium, magnesium, manganese, iron, copper, sodium and potassium.

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This document provides guidelines for the laboratory refining of various pulps intended for paper production including: - Harmonization of terms and parameters for the simulation of industrial refining processes by laboratory refiners; - Treatment of pulp samples in a (semi) continuous operation in contrast to the batch operation of laboratory beating equipment such as the PFI mill; - Evaluation of fibres for papermaking, in particular chemical market pulps, under close-to-reality conditions in terms of refining intensity and refining energy consumption. This document only considers refiners operating at low stock concentration, i.e. 3 % to 5 %.

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This document specifies a method for the determination of the conductivity of aqueous extracts of paper, board or pulp, these extracts having been prepared by a hot or cold method.
The method is applicable to all kinds of paper, board and pulps, except for papers used for electrical purposes. For high purity papers used for electrical purposes, see method given in EN 60554‑2.

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  • Standard
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This document specifies a method for the determination of the pH-value defined by the electrolytes extractable by hot water from a sample of paper, board or pulp.
This document is applicable to all kinds of paper, board and pulp.
As the quantity of extractable ionic material approaches zero, as in the case of highly purified pulps, the precision of the method becomes poor because of the difficulties encountered in making pH measurements on water containing little electrolytic material.
Since the extraction in this document is performed with distilled or deionised water, the pH-value measured can sometimes be different (e.g. fully bleached pulp) from the pH-value measured under mill process conditions in which various types of process waters, such as chemically treated river water containing electrolytes, are used. In such cases, ISO 29681 can be used instead, as it is specifically applicable to bleached pulps from virgin fibres and to pulp samples having a low ionic strength for which the pH value gives more realistic results related to mill conditions than those obtained with this document. For cellulosic papers used for electrical purposes, the method used can be that given in IEC 60554-2[5].

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This document specifies a method for the determination of the pH-value defined by the electrolytes extractable by cold water from a sample of paper, board or pulp.
This document is applicable to all types of paper, board and pulp.
As the quantity of extractable ionic material approaches zero, as in the case of highly purified pulps, the precision of the method becomes poor because of the difficulties encountered in making pH measurements on water containing little electrolytic material.
Since the extraction in this document is performed with distilled or deionised water, the pH-value measured can sometimes be different (e.g. for fully bleached pulp) from the pH-value measured under mill process conditions, in which various types of process waters, such as chemically treated river water containing electrolytes, are used. In such cases, ISO 29681 can be used instead, as it is specifically applicable to bleached pulps from virgin fibres and to pulp samples having a low ionic strength for which the pH value gives more realistic results related to mill conditions than those obtained with this document.
For cellulosic papers used for electrical purposes, the method used can be that given in IEC 60554‑2[5].

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This document specifies the standard atmospheres for conditioning and testing pulp, paper and board, the conditioning procedure and the procedures for measuring the temperature and relative humidity.

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This document specifies a method for determining the bacteria, yeast and mould population on the surface of paper and paperboard. The enumeration relates to specific media. This document is applicable to all kinds of paper and paperboard, to dry market pulp in sheet form and to packaging material.

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This document specifies an apparatus and the procedures for the laboratory wet disintegration of mechanical pulps that exhibit latency except when brightness is measured. This apparatus and procedure can be used for preparation of the test portion in other International Standards dealing with pulps.
This document is applicable to all kind of mechanical pulps (i.e. mechanical, semi-chemical and chemi-mechanical pulps) exhibiting latency.

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This document specifies a potentiometric titration procedure for the determination of total, active and effective alkali in white and green liquors obtained and used in the kraft or sulphate pulping process. This document is not applicable for the analysis of liquors such as oxidized white liquors which contain significant amounts of polysulphides. The method given in this document is not intended for the determination of particular ionic species, such as sulphides or carbonates.

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This document describes a procedure for the determination of sulphide, i.e. the hydrosulphide ion concentration, in white, oxidized white and green liquors, as well as in black liquor having a dry matter content up to 40 %. The determination also includes the sulphide part of any polysulphide present in the solution.

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This document describes a procedure for determining the content of residual alkali in Kraft black liquors having a dry matter content up to 40 %. The method is based on a potentiometric titration with hydrochloric acid and is intended for black liquor samples with an initial pH ≥ 11,0. The lower limit of determination is 0,1 g/l of eq. NaOH.

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This document specifies an apparatus and the procedures for the laboratory wet disintegration of mechanical pulps that exhibit latency except when brightness is measured. This apparatus and procedure can be used for preparation of the test portion in other International Standards dealing with pulps.
This document is applicable to all kind of mechanical pulps (i.e. mechanical, semi-chemical and chemi-mechanical pulps) exhibiting latency.

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This document specifies an apparatus and the procedures for the laboratory wet disintegration of mechanical pulps that exhibit latency except when brightness is measured. This apparatus and procedure can be used for preparation of the test portion in other International Standards dealing with pulps. This document is applicable to all kind of mechanical pulps (i.e. mechanical, semi-chemical and chemi-mechanical pulps) exhibiting latency.

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This document specifies the general procedure for fibre furnish analysis of paper, board and pulps. It is applicable to all kinds of pulps and to most papers and boards, including those containing more than one kind of fibre, taking into account different pulping processes. This method is less suitable for heavily impregnated or highly coloured papers and boards, which cannot be dispersed or decoloured without affecting the structure or the staining reactions of the fibres.

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This document specifies the standard atmospheres for conditioning and testing pulp, paper and board, the conditioning procedure and the procedures for measuring the temperature and relative humidity.

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This document describes the determination of the residue (ash content) on ignition of paper, board, pulps and cellulose nanomaterials at 525 °C. It is applicable to all types of paper, board, pulp and cellulose nanomaterial samples.
This document provides measurement procedures to obtain a measurement precision of 0,01 % or better for residue (ash content) on ignition at 525 °C.
Determination of residue (ash content) on ignition at 900 °C of paper, board, pulps and cellulose nanomaterials is described in ISO 2144.
In the context of this document, the term "cellulose nanomaterial" refers specifically to cellulose nano-object (see 3.2 to 3.4). Owing to their nanoscale dimensions, these cellulose nano-objects can have intrinsic properties, behaviours or functionalities that are distinct from those associated with paper, board and pulps.

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This document specifies two procedures for the preparation of laboratory sheets prior to measuring optical properties. One is the preparation of pads in a Büchner funnel using a filter paper or a wire screen and the other one is the preparation of laboratory sheets in a standard sheet former (conventional or Rapid Köthen). This document is applicable to all wood pulps and to most other types of pulp. It is not applicable to pulps with very long fibres, such as those made from unshortened cotton, flax and similar materials, unless they are reduced to a suitable fibre length (about 2 mm) before performing the methods. It is not applicable to recycled pulps (see ISO 21993). It is not applicable to opacity measurements or to the determination of light scattering and absorption coefficients.

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SIGNIFICANCE AND USE
5.1 Moisture analysis (along with purity) is used to calculate the amount of active polymer in the material and must be considered when determining the amount of sodium carboxymethylcellulose to use in various formulations.
SCOPE
1.1 These test methods cover the testing of sodium carboxymethylcellulose.  
1.2 The test procedures appear in the following order:    
Sections  
Moisture  
4 – 9  
Degree of Etherification:  
Test Method A—Acid Wash  
10 – 17  
Test Method B—Nonaqueous Titration  
10, 12, 18 – 23  
Viscosity  
24 – 29  
Purity  
30 – 37  
Sodium Glycolate  
38 – 46  
Sodium Chloride  
47 – 54  
Density  
55 – 61  
1.3 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. For specific hazard statements, see 15.1 and 20.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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This document specifies the standard atmospheres for conditioning and testing pulp, paper and board, the conditioning procedure and the procedures for measuring the temperature and relative humidity.

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This document specifies an oven-drying method for the determination of the dry matter content in paper, board, pulp and cellulosic nanomaterials in solid form, which all can be produced from virgin and /or recycled materials.
It is also applicable to the determination of the dry matter content of paper and board for recycling.
The procedure is applicable to paper, board, and pulp and cellulosic nanomaterials which do not contain any appreciable quantities of materials other than water that are volatile at the temperature of 105 °C ± 2 °C. It is used, for example, in the case of pulp, paper, and board and cellulosic nanomaterial samples taken for chemical and physical tests in the laboratory, when a concurrent determination of dry matter content is required.
This method is not applicable to the determination of the dry matter content of slush pulp or to the determination of the saleable mass of pulp lots.
NOTE 1    ISO 638-2[1] specifies an oven-drying method for the determination of the dry matter content of suspensions of cellulosic nanomaterials, ISO 287[2] specifies the determination of the moisture content of a lot of paper and board; ISO 4119[3] specifies the determination of stock concentration of pulps; the ISO 801 series[4] specifies the determination of the saleable mass in lots.
NOTE 2    This document determines the total dry matter content of the sample, including any dissolved solids. If only the cellulosic material content free of dissolved solids is desired, dissolved solids are removed prior to measuring the dry matter content, e.g. by washing or dialysis, taking care to retain all cellulosic material; in cases where the sample is filterable without loss of cellulosic solids, ISO 4119[3] can be used to determine the stock consistency (content of cellulosic material in solid form).

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This document specifies the standard atmospheres for conditioning and testing pulp, paper and board, the conditioning procedure and the procedures for measuring the temperature and relative humidity.

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This document specifies the relevant International Standards used for the determination of physical properties of laboratory sheets made of all types of pulps.
It is applicable to laboratory sheets prepared in accordance with ISO 5269‑1, ISO 5269‑2 or ISO 5269‑3.

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This document specifies an oven-drying method for the determination of the dry matter content in suspensions of cellulosic nanomaterials. The procedure is applicable to cellulosic nanomaterial suspensions which do not contain any appreciable quantities of materials other than water that are volatile at the temperature of 105 °C ± 2 °C. It is used, for example, in the case of cellulosic nanomaterial suspensions samples taken for chemical and physical tests in the laboratory, when a concurrent determination of dry matter content is required.
NOTE      This document determines the total dry matter content of the sample, including any dissolved solids. If only the cellulosic material content free of dissolved solids is desired, dissolved solids are removed prior to measuring the dry matter content, e.g. by washing or dialysis, taking care to retain all cellulosic material.

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This document specifies the relevant International Standards used for the determination of physical properties of laboratory sheets made of all types of pulps.
It is applicable to laboratory sheets prepared in accordance with ISO 5269‑1, ISO 5269‑2 or ISO 5269‑3.

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This document specifies the relevant International Standards used for the determination of physical properties of laboratory sheets made of all types of pulps. It is applicable to laboratory sheets prepared in accordance with ISO 5269‑1, ISO 5269‑2 or ISO 5269‑3.

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This document specifies a method of obtaining, for test purposes, a gross sample representative of a certain lot of pulp. This document applies to all kinds of pulp delivered in bales or rolls. It is intended for use when sampling for all kinds of testing purposes except for the determination of saleable mass, in which case other International Standards apply such as ISO 801-1 and ISO 801-2.
If, however, the pulp is to be tested for saleable mass in addition to other properties, the gross sample obtained according to the appropriate International Standard for sampling saleable mass can also be used for the other pulp property tests.

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This document describes a method for the determination of lignin content in kraft, soda, and hydrolysis lignin. The method is applicable to lignin isolated from a kraft pulping process, a soda pulping process, or lignin obtained by hydrolysis of biomass.

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SIGNIFICANCE AND USE
5.1 This test method is suitable for use as a rapid control test for pulp manufacture or for careful determination of the viscometric molecular weight of purified cotton or wood derived pulps.  
5.2 This test method is applicable over a very large range of cellulose molecular weights because seven sample sizes are defined. (Sample weights are reduced as cellulose molecular weight increases.)  
5.3 Cotton and high molecular weight pulps may be difficult to dissolve. (Warning—This test method is only valid if the sample dissolves completely without gels.)
SCOPE
1.1 This test method describes the procedure for estimating the molecular weight of cellulose by determining the viscosity of cuprammonium (CuAm) solutions of cellulosic materials, such as wood pulp, cotton, and cotton linters. This test method is suitable for rapid, routine testing of large numbers of samples with high accuracy and precision. This test method updates and extends the procedure reported by the American Chemical Society (ACS).2  
1.2 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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This document describes a method for the determination of carbohydrate composition in kraft lignin, soda lignin and biorefinery lignin. The method is applicable to lignin isolated from a kraft pulping process, a soda pulping process, or lignin obtained by hydrolysis of biomass.

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This document specifies an oven-drying method for the determination of the dry matter content in paper, board, pulp and cellulosic nanomaterials in solid form, which all can be produced from virgin and /or recycled materials.
It is also applicable to the determination of the dry matter content of paper and board for recycling.
The procedure is applicable to paper, board, and pulp and cellulosic nanomaterials which do not contain any appreciable quantities of materials other than water that are volatile at the temperature of 105 °C ± 2 °C. It is used, for example, in the case of pulp, paper, and board and cellulosic nanomaterial samples taken for chemical and physical tests in the laboratory, when a concurrent determination of dry matter content is required.
This method is not applicable to the determination of the dry matter content of slush pulp or to the determination of the saleable mass of pulp lots.
NOTE 1    ISO 638-2[1] specifies an oven-drying method for the determination of the dry matter content of suspensions of cellulosic nanomaterials, ISO 287[2] specifies the determination of the moisture content of a lot of paper and board; ISO 4119[3] specifies the determination of stock concentration of pulps; the ISO 801 series[4] specifies the determination of the saleable mass in lots.
NOTE 2    This document determines the total dry matter content of the sample, including any dissolved solids. If only the cellulosic material content free of dissolved solids is desired, dissolved solids are removed prior to measuring the dry matter content, e.g. by washing or dialysis, taking care to retain all cellulosic material; in cases where the sample is filterable without loss of cellulosic solids, ISO 4119[3] can be used to determine the stock consistency (content of cellulosic material in solid form).

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This document specifies an oven-drying method for the determination of the dry matter content in suspensions of cellulosic nanomaterials. The procedure is applicable to cellulosic nanomaterial suspensions which do not contain any appreciable quantities of materials other than water that are volatile at the temperature of 105 °C ± 2 °C. It is used, for example, in the case of cellulosic nanomaterial suspensions samples taken for chemical and physical tests in the laboratory, when a concurrent determination of dry matter content is required.
NOTE      This document determines the total dry matter content of the sample, including any dissolved solids. If only the cellulosic material content free of dissolved solids is desired, dissolved solids are removed prior to measuring the dry matter content, e.g. by washing or dialysis, taking care to retain all cellulosic material.

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This document specifies a method for determining the total number of colony-forming units of yeast and mould in dry market pulp, paper and paperboard after disintegration. The enumeration relates to specific media.

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This document specifies an oven-drying method for the determination of the dry matter content in paper, board, pulp and cellulosic nanomaterials in solid form, which all can be produced from virgin and /or recycled materials. It is also applicable to the determination of the dry matter content of paper and board for recycling. The procedure is applicable to paper, board, and pulp and cellulosic nanomaterials which do not contain any appreciable quantities of materials other than water that are volatile at the temperature of 105 °C ± 2 °C. It is used, for example, in the case of pulp, paper, and board and cellulosic nanomaterial samples taken for chemical and physical tests in the laboratory, when a concurrent determination of dry matter content is required. This method is not applicable to the determination of the dry matter content of slush pulp or to the determination of the saleable mass of pulp lots. NOTE 1 ISO 638-2[1] specifies an oven-drying method for the determination of the dry matter content of suspensions of cellulosic nanomaterials, ISO 287[2] specifies the determination of the moisture content of a lot of paper and board; ISO 4119[3] specifies the determination of stock concentration of pulps; the ISO 801 series[4] specifies the determination of the saleable mass in lots. NOTE 2 This document determines the total dry matter content of the sample, including any dissolved solids. If only the cellulosic material content free of dissolved solids is desired, dissolved solids are removed prior to measuring the dry matter content, e.g. by washing or dialysis, taking care to retain all cellulosic material; in cases where the sample is filterable without loss of cellulosic solids, ISO 4119[3] can be used to determine the stock consistency (content of cellulosic material in solid form).

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This document specifies an oven-drying method for the determination of the dry matter content in suspensions of cellulosic nanomaterials. The procedure is applicable to cellulosic nanomaterial suspensions which do not contain any appreciable quantities of materials other than water that are volatile at the temperature of 105 °C ± 2 °C. It is used, for example, in the case of cellulosic nanomaterial suspensions samples taken for chemical and physical tests in the laboratory, when a concurrent determination of dry matter content is required. NOTE This document determines the total dry matter content of the sample, including any dissolved solids. If only the cellulosic material content free of dissolved solids is desired, dissolved solids are removed prior to measuring the dry matter content, e.g. by washing or dialysis, taking care to retain all cellulosic material.

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This document specifies a method of obtaining, for test purposes, a gross sample representative of a certain lot of pulp. This document applies to all kinds of pulp delivered in bales or rolls. It is intended for use when sampling for all kinds of testing purposes except for the determination of saleable mass, in which case other International Standards apply such as ISO 801-1 and ISO 801-2.
If, however, the pulp is to be tested for saleable mass in addition to other properties, the gross sample obtained according to the appropriate International Standard for sampling saleable mass can also be used for the other pulp property tests.

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This document presents guidelines for a methodology for the estimation of the uncertainty of methods for testing lignins and kraft liquors, pulps, paper, board, cellulosic nanomaterials, as well as products thereof containing any portion of recycled material or material intended for recycling.

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This document specifies a method of obtaining, for test purposes, a gross sample representative of a certain lot of pulp. This document applies to all kinds of pulp delivered in bales or rolls. It is intended for use when sampling for all kinds of testing purposes except for the determination of saleable mass, in which case other International Standards apply such as ISO 801-1 and ISO 801-2. If, however, the pulp is to be tested for saleable mass in addition to other properties, the gross sample obtained according to the appropriate International Standard for sampling saleable mass can also be used for the other pulp property tests.

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This document specifies a method for the determination of the pH-value defined by the electrolytes extractable by cold water from a sample of paper, board or pulp. This document is applicable to all types of paper, board and pulp. As the quantity of extractable ionic material approaches zero, as in the case of highly purified pulps, the precision of the method becomes poor because of the difficulties encountered in making pH measurements on water containing little electrolytic material. Since the extraction in this document is performed with distilled or deionised water, the pH-value measured can sometimes be different (e.g. for fully bleached pulp) from the pH-value measured under mill process conditions, in which various types of process waters, such as chemically treated river water containing electrolytes, are used. In such cases, ISO 29681 can be used instead, as it is specifically applicable to bleached pulps from virgin fibres and to pulp samples having a low ionic strength for which the pH value gives more realistic results related to mill conditions than those obtained with this document. For cellulosic papers used for electrical purposes, the method used can be that given in IEC 60554‑2[5].

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This document specifies a method for the determination of the pH-value defined by the electrolytes extractable by hot water from a sample of paper, board or pulp. This document is applicable to all kinds of paper, board and pulp. As the quantity of extractable ionic material approaches zero, as in the case of highly purified pulps, the precision of the method becomes poor because of the difficulties encountered in making pH measurements on water containing little electrolytic material. Since the extraction in this document is performed with distilled or deionised water, the pH-value measured can sometimes be different (e.g. fully bleached pulp) from the pH-value measured under mill process conditions in which various types of process waters, such as chemically treated river water containing electrolytes, are used. In such cases, ISO 29681 can be used instead, as it is specifically applicable to bleached pulps from virgin fibres and to pulp samples having a low ionic strength for which the pH value gives more realistic results related to mill conditions than those obtained with this document. For cellulosic papers used for electrical purposes, the method used can be that given in IEC 60554-2[5].

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This document specifies a method for the determination of the conductivity of aqueous extracts of paper, board or pulp, these extracts having been prepared by a hot or cold method. The method is applicable to all kinds of paper, board and pulps, except for papers used for electrical purposes. For high purity papers used for electrical purposes, see method given in EN 60554‑2.

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This document specifies an analytical test method for the determination of anthraquinone (see Table 1) in water and 95 % ethanol extracts of pulp, paper and board materials and articles intended to come into contact with foodstuffs using a gas chromatograph coupled to a mass spectrometer (GC-MS). Moreover, acetone extracts of modified polyphenylene oxide (MPPO) that, according to EN 14338, can be used as a simulant to assess the possible transfer/migration of substances from paper and board into dry, non-fatty foodstuffs can be analysed with the method presented here.
This method can be applied to determine anthraquinone in concentrations ranging from 2 μg/l to 40 μg/l in the water and solvent extracts, corresponding to 0,05 mg/kg to 1 mg/kg pulp, paper and board or, respectively, 0,1 μg/dm2 to 2 μg/dm2 in the case of migration tests with MPPO. The measurement range can be lowered by enriching anthraquinone from the water and solvent extracts.

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SIGNIFICANCE AND USE
4.1 Manganese in pulp acts as a catalyst in oxidizing cellulose.  
4.2 Iron in pulp can cause yellowness in rayon fibers and influence cellulose acetate plastics color. Iron also causes problems in photographic and blueprint papers.  
4.3 Copper in pulp can act as a retardant in oxidizing cellulose and can affect viscose ripening. Copper interferes with the dye level of rayon fibers and influences cellulose acetate plastics color.  
4.4 Calcium in pulps can cause problems in processing into acetate, rayon, cellophane, etc. Calcium can create undesirable deposits in viscose spinning and film casting operation. Calcium can influence viscosity control during cellulose acetate manufacture.
SCOPE
1.1 This test method covers the determination of the iron, copper, manganese, and calcium content of cellulose pulp from wood or cotton.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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SIGNIFICANCE AND USE
5.1 The results of this test are used for calculating the total solids in the sample; and, by common usage, all materials volatile at this test temperature are designated as moisture.  
5.2 Moisture analysis (along with sulfated ash) is a measure of the amount of active polymer in the material and must be considered when determining the amount of hydroxyethyl cellulose to use in various formulations.
SCOPE
1.1 These test methods cover the testing of hydroxyethylcellulose.  
1.2 The test procedures appear in the following order:    
Sections  
Moisture  
4 – 9  
Ash  
10 – 17  
Viscosity  
18 – 23    
Density  
24 – 30  
1.3 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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