EP2270281A1 - Process for dyeing pulp - Google Patents

Process for dyeing pulp Download PDF

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Publication number
EP2270281A1
EP2270281A1 EP09163790A EP09163790A EP2270281A1 EP 2270281 A1 EP2270281 A1 EP 2270281A1 EP 09163790 A EP09163790 A EP 09163790A EP 09163790 A EP09163790 A EP 09163790A EP 2270281 A1 EP2270281 A1 EP 2270281A1
Authority
EP
European Patent Office
Prior art keywords
pulp
weight
basic
fluorescent whitening
whitening agent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP09163790A
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German (de)
French (fr)
Inventor
Klaus-Günter Strumpf
Inge Spitzlay
Helmut-Martin Meier
Martina Niemuth
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kemira Germany GmbH
Original Assignee
Kemira Germany GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kemira Germany GmbH filed Critical Kemira Germany GmbH
Priority to EP09163790A priority Critical patent/EP2270281A1/en
Priority to PCT/EP2010/059070 priority patent/WO2010149773A1/en
Publication of EP2270281A1 publication Critical patent/EP2270281A1/en
Withdrawn legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
    • D21H21/28Colorants ; Pigments or opacifying agents
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
    • D21H21/30Luminescent or fluorescent substances, e.g. for optical bleaching

Definitions

  • the present invention relates to a process for dyeing pulp and a paper obtained by this process.
  • cationic dyes for dyeing paper.
  • the cationic dyes used are usually di- or triarylmethine dyes, which are also known as triaryl methane dyes or triaryl carbenium ions, oxazine dyes, thiazine dyes, acridine, xanthene, or thioxanthene dyes, rhodamine dyes, azo dyes having basic groups, such as C.I. Basic Brown 1, styryl dyes, such as Basic Yellow 90, as described in P. Rys, H. Zollinger, Fundamentals of the Chemistry and Application of Dyes, Wiley Interscience, London, 1972 . Commonly used dyes are further described in Klaus Hunger (Editor), Industrial Dyes, Wiley-VCH, Weinheim, 2003 .
  • US-A- 4 374 643 describes colour salts or complexes consisting of an optical brightener component having an anionic group and a colour component having a basic group capable of forming a salt with the anionic group. These salts are hardly or not soluble in water, and can be used for colouring various fibrous articles.
  • the abovementioned cationic dyes exhibit a large affinity to wood-containing, unbleached paper fibres. Therefore, they are used for dyeing wood-containing papers, e.g. packaging, kraft, sleeve, and envelope papers.
  • wood-containing papers e.g. packaging, kraft, sleeve, and envelope papers.
  • bleached, wood-free pulp exhibits insufficient dyeing behaviour with respect to cationic dyes ( Klaus Hunger (Editor), Industrial Dyes, Wiley-VCH, Weinheim, 2003, page 460 ).
  • FWA fluorescent whitening agent
  • the present invention relates to a process for dyeing pulp comprising bleached pulp, comprising adding at least one cationic dye to the pulp, and then adding at least one fluorescent whitening agent to the pulp, followed by forming the paper sheet. Further, the invention relates to a paper obtainable by the process according to the invention. Preferred embodiments of the invention are described in the description hereinafter, the examples and the dependent claims.
  • the pulp that can be used in the process of the invention is any pulp or pulp suspension which comprises bleached pulp or is at least partially bleached pulp.
  • the pulp can be produced from softwood or pine wood, hardwood, grasses, used or waste paper, or exotic fibres, such as hemp, jute, cotton, palms, agave, sisal, or coconut, according to conventional processes, e.g. as described in M. J. Kocurek, Pulp and Paper Manufacture, Vol. 1, Joint textbook Committee of the Paper Industry; Tappi CPPA 1983 .
  • the cellulose is obtained by removing the lignin components during pulping and other interfering substances during bleaching.
  • a pulp can be produced by reacting or cooking wood chips with an alkaline cooking liquid at elevated temperature.
  • the cooking liquor may be a kraft, soda, alkali, sulfite or polysulfide cooking liquor, or a modification thereof, for example an anthraquinone modified cooking liquor.
  • Known processes are e.g. the sulfate or sulfite processes, or bleaching processes, such as described e.g. in J. S. Gratzl, Chemischemaschinen der Zellstoffbleiche mit Sauerstoff, Wasserstoffperoxid und Ozon, Das Textil 46, V1-V8(1992), Nr. 10A .
  • Lignin which is a component of the wood used, is dissolved by the cooking liquor.
  • the character of the pulp produced is dependent on the amount of lignin removal from the wood used, and thus depends on the residual lignin content of the final pulp.
  • the Kappa number represents a measure for the residual lignin content of a pulp.
  • the Kappa number can be determined by the standard test method ISO 302:2004 Pulps - Determination of Kappa number. Higher Kappa numbers indicate higher residual lignin contents.
  • Pulps suitable in the process of the invention are pulps which contain at least 10 % by weight of bleached pulp based on 100 % by weight of the pulp used. Depending on how far the effects of the invention should be obtained, it is also possible to work with lower amounts of bleached pulp.
  • Preferred pulps contain at least 20 % by weight of bleached pulp, based on 100 % by weight of the pulp.
  • the pulp used consists of bleached pulp or is a wood-free pulp.
  • wood-free as employed in the paper making art and as used herein means pulps which are free or essentially free of lignin, and in particular pulps which have a lignin content of less than 1 % by weight. If a pulp is bleached, it is necessarily also wood-free.
  • Pulps suitable in the process of the invention are pulps containing 0.1 to 50 % by weight, preferably 0.5 to 40 % by weight, in particular 1 to 10 % by weight of fibers, based on 100 % by weight of the pulp.
  • pulps suitable in the process of the invention are pulps having Kappa numbers up to 160, preferably in the range of 135 to 0, more preferably 100 to 0, most preferably 50 to 0.
  • Cationic dyes which can be used in the process of the invention are the cationic dyes as known from the prior art and as described above.
  • cationic dye means, in line with the common understanding in the art, that the dye is derived from dye bases. Cationic dyes form positively charged ions (cations) by dissociation in water. The term “cationic dye” does not refer to the pH reaction of these dyes.
  • Suitable cationic dyes are the following cationic dyes, which are described according to the Color Index: Basic Blue 3, Basic Blue 26, Basic Blue 41, Basic Blue 54, Basic Blue 64, Basic Blue 100, Basic Blue 140, Basic Blue 159, Basic Blue 163, Basic Green 1, Basic Green 4, Basic Orange 1, Basic Orange 2, Basic Orange 21, Basic Orange 60, Basic Orange 64, Basic Orange 160, Basic Red 1, Basic Red 12, Basic Red 14, Basic Red 18, Basic Red 29, Basic Red 46, Basic Red 49, Basic Red 51, Basic Red 108, Basic Red 111, Basic Violet 1, Basic Violet 3, Basic Violet 4, Basic Violet 10, Basic Violet 14, Basic Violet 16, Basic Violet 49, Basic Yellow 1, Basic Yellow 11, Basic Yellow 13, Basic Yellow 15, Basic Yellow 21, Basic Yellow 28, Basic Yellow 29, Basic Yellow 40, Basic Yellow 51, Basic Yellow 70, Basic Yellow 94, Basic Yellow 96, Basic Brown 1, Basic Brown 22, and Basic Brown 23.
  • Preferred cationic dyes are Basic Blue 159, Basic Blue 26, Basic Red 12, Basic Violet 16, Basic Red 49, Basic Violet 1, and Basic Yellow 90. The following cationic dyes which are indicated by their formulas are also preferred.
  • Suitable amounts of cationic dye are within a range of 0.01 to 20 % by weight based on 100 % by weight of the pulp used.
  • the cationic dye is used in an amount of 0.01 to 1 % by weight or in an amount of 0.05 to 10 % by weight, preferably 0.1 to 1 % by weight, more preferred 0.2 to 0.5 % by weight, based on 100 % by weight of the pulp.
  • One or more cationic dyes can be used as a cationic dye.
  • the fluorescent whitening agents that can be used in the process of the invention are known fluorescent whitening agents and are subject to no limitations. Suitable fluorescent whitening agents are described in e.g. Klaus Hunger (Editor), Industrial Dyes, Wiley-VCH, Weinheim, 2003, Chapter 7.2, pages 590-610 . In particular, fluorescent whitening agents having sulfonic acid residues are suitable.
  • sulfonic acid groups-containing distyrylbenzenes distyrylbiphenyls, divinylstilbenes, triazinylaminostilbenes, stilbenyl-2H-triazoles, stilbenyl-2H-naphtho[1,2-d]triazoles, bis(1,2,3-triazol-2-yl)stilbenes, benzoxazoles, stilbenylbenzoxazoles, bis-benzoxazoles, bis(benzo[b]furan-2-yl)biphenyls, benzimidazoles, 1,3-diphenyl-2-pyrazolines, coumarins, und naphthalimides.
  • the fluorescent whitening agent is a derivative of 4,4'-diaminostilbene-2,2'-disulfonic acid, in particular a 1,3,5-triazinyl derivative of 4,4'-diaminostilbene-2,2'-disulfonic acid or salts thereof.
  • disodium salt of 4,4'-bis[(4-anilino-6-diethanolamino-1,3,5-triazine-2-yl)amino]-stilbene-2,2'-disulfonic acid the tetrasodium and hexasodium salt of 4,4'-bis[(4-p-sulfoanilino-6-diethanolamino-1,3,5-triazine-2-yl)amino]-stilbene-2,2'-disulfonic acid
  • hexasodium salt of 4,4'-bis[(4-(2,5-disulfoanilino)-6-diethanolamino-1,3,5-triazine-2-yl)amino]-stilbene-2,2'-disulfonic acid the disodium salt of 4,4'-bis[(4-anilino-6-diethanolamino-1,3,5-triazine-2-yl)amino]
  • Suitable amounts of fluorescent whitening agent are within a range of 0.001 to 10 % by weight based on 100 % by weight of the pulp.
  • the fluorescent whitening agent is used in an amount of 0.01 to 5 % by weight, preferably 0.1 to 1 % by weight, more preferably 0.2 to 0.4 % by weight, based on 100 % by weight of the pulp.
  • fluorescent whitening agent one or more fluorescent whitening agents can be used.
  • the process of the invention is carried out by adding the cationic dye to the pulp, and then adding the fluorescent whitening agent.
  • the cationic dye and/or fluorescent whitening agent are suitably added by mixing or agitating. If the fluorescent whitening agent is added to the pulp with the added cationic dye too fast, a precipitate of fluorescent whitening agent and cationic dye is formed. Therefore, according to the invention the fluorescent whitening agent is suitably added to the pulp with the added cationic dye at a time at which no such precipitate is formed. This is usually after an agitation time in which the cationic dye has been sufficiently distributed in the pulp, and this depends on the agitation performance.
  • the fluorescent whitening agent is added some seconds or minutes, e.g. 30 seconds, or 1, 2, 3, 5, 10, 15 or 20 minutes, after the cationic dye has been added. In particular, the fluorescent whitening agent is added 5 to 10 minutes after the cationic dye addition. After that the paper sheet is formed.
  • the dye and/or fluorescent whitening agent can be added to the pulp in the paper machine in the pulper, in the mixing vat, in the stuff chest, before the headbox, or in the size press.
  • the process of the invention can be carried out continuously, discontinuously (batch), or a combination of both by split dyeing. In the discontinuous process the dyeing is usually carried out batch wise in the pulper or the mixing vat. In the continuous process the dyeing is usually carried out by adding the dye and fluorescent whitening agent to the pulp stream.
  • the dye and fluorescent whitening agent can be added in the thick matter area and/or thin (dilute) matter area. It is further possible to dye both in the pulp and on the surface.
  • Surface dyeing or dipping can be carried out by using coating colours and e.g. a size press. It is possible to use coating colors with dye and fluorescent whitening agent. Further, it is possible to soak the base paper with dyeing solution and fluorescent whitening agent in a dipping tank, or to carry out a dyeing application in the plane using suitable printing procedures.
  • the present invention surprisingly overcomes the problem that bleached wood-free pulp is insufficiently dyed by cationic dyes.
  • a fluorescent whitening agent is added in an amount as indicated in the Tables below (the amount refers to % by weight based on 100 % by weight of the pulp). After 20 to 30 seconds the sheet is formed.
  • the fluorescent whitening agent used is BLANKOPHOR DS, which contains the disodium salt of 4,4'-bis[(4-anilino-6-diethanolamino-1,3,5-triazine-2-yl)amino]-stilbene-2,2'-disulfonic acid.
  • MESITOL P which is a commercial polycondensate of naphthalene sulfonic acid and formaldehyde
  • MESITOL NBS which is a commercial polycondensate of phenol sulfonic acid, 4,4'-dihydroxydiphenyl sulfone and formaldehyde
  • Both fixing agents are present as sodium salts.
  • the % data hereinafter refer to percent by weight.
  • the colour measurements are carried out with the CIELab system according to DIN 6174.
  • the samples of the invention with fluorescent whitening agent exhibit higher ⁇ C values.
  • the colour is more brilliant, compared to the comparative samples with the anionic fixing agents MESITOL, which result in less brilliant colourings.
  • dyeing bleached wood-free pulp with cationic dyes results in brilliant dyeing when using fluorescent whitening agents.

Abstract

The invention relates to a process for dyeing pulp comprising bleached pulp comprising adding a cationic dye to the pulp, and then adding a fluorescent whitening agent, followed by forming the paper sheet. Further, the invention relates to a paper obtained by this process.

Description

  • The present invention relates to a process for dyeing pulp and a paper obtained by this process.
  • It is known in the art to use cationic dyes for dyeing paper. The cationic dyes used are usually di- or triarylmethine dyes, which are also known as triaryl methane dyes or triaryl carbenium ions, oxazine dyes, thiazine dyes, acridine, xanthene, or thioxanthene dyes, rhodamine dyes, azo dyes having basic groups, such as C.I. Basic Brown 1, styryl dyes, such as Basic Yellow 90, as described in P. Rys, H. Zollinger, Fundamentals of the Chemistry and Application of Dyes, Wiley Interscience, London, 1972. Commonly used dyes are further described in Klaus Hunger (Editor), Industrial Dyes, Wiley-VCH, Weinheim, 2003.
  • US-A- 4 374 643 describes colour salts or complexes consisting of an optical brightener component having an anionic group and a colour component having a basic group capable of forming a salt with the anionic group. These salts are hardly or not soluble in water, and can be used for colouring various fibrous articles.
  • The abovementioned cationic dyes exhibit a large affinity to wood-containing, unbleached paper fibres. Therefore, they are used for dyeing wood-containing papers, e.g. packaging, kraft, sleeve, and envelope papers. On the other hand, it is also known that bleached, wood-free pulp exhibits insufficient dyeing behaviour with respect to cationic dyes (Klaus Hunger (Editor), Industrial Dyes, Wiley-VCH, Weinheim, 2003, page 460).
  • Surprisingly, it has been found that this problem can be overcome by using a fluorescent whitening agent (FWA).
  • Accordingly, the present invention relates to a process for dyeing pulp comprising bleached pulp, comprising adding at least one cationic dye to the pulp, and then adding at least one fluorescent whitening agent to the pulp, followed by forming the paper sheet. Further, the invention relates to a paper obtainable by the process according to the invention. Preferred embodiments of the invention are described in the description hereinafter, the examples and the dependent claims.
  • The pulp that can be used in the process of the invention is any pulp or pulp suspension which comprises bleached pulp or is at least partially bleached pulp. The pulp can be produced from softwood or pine wood, hardwood, grasses, used or waste paper, or exotic fibres, such as hemp, jute, cotton, palms, agave, sisal, or coconut, according to conventional processes, e.g. as described in M. J. Kocurek, Pulp and Paper Manufacture, Vol. 1, Joint textbook Committee of the Paper Industry; Tappi CPPA 1983. In the production of wood-free pulp the cellulose is obtained by removing the lignin components during pulping and other interfering substances during bleaching. A pulp can be produced by reacting or cooking wood chips with an alkaline cooking liquid at elevated temperature. The cooking liquor may be a kraft, soda, alkali, sulfite or polysulfide cooking liquor, or a modification thereof, for example an anthraquinone modified cooking liquor. Known processes are e.g. the sulfate or sulfite processes, or bleaching processes, such as described e.g. in J. S. Gratzl, Chemische Grundlagen der Zellstoffbleiche mit Sauerstoff, Wasserstoffperoxid und Ozon, Das Papier 46, V1-V8(1992), Nr. 10A. Lignin, which is a component of the wood used, is dissolved by the cooking liquor. The character of the pulp produced is dependent on the amount of lignin removal from the wood used, and thus depends on the residual lignin content of the final pulp. The Kappa number represents a measure for the residual lignin content of a pulp. The Kappa number can be determined by the standard test method ISO 302:2004 Pulps - Determination of Kappa number. Higher Kappa numbers indicate higher residual lignin contents.
  • Pulps suitable in the process of the invention are pulps which contain at least 10 % by weight of bleached pulp based on 100 % by weight of the pulp used. Depending on how far the effects of the invention should be obtained, it is also possible to work with lower amounts of bleached pulp. Preferred pulps contain at least 20 % by weight of bleached pulp, based on 100 % by weight of the pulp. In particular, there is used a pulp containing 50 to 100 % by weight, preferably 90 to 100 % by weight, more preferably 95 to 100 % by weight, of bleached pulp, based on 100 % by weight of the pulp used. In a preferred embodiment, the pulp used consists of bleached pulp or is a wood-free pulp. The term "wood-free" as employed in the paper making art and as used herein means pulps which are free or essentially free of lignin, and in particular pulps which have a lignin content of less than 1 % by weight. If a pulp is bleached, it is necessarily also wood-free.
  • Pulps suitable in the process of the invention are pulps containing 0.1 to 50 % by weight, preferably 0.5 to 40 % by weight, in particular 1 to 10 % by weight of fibers, based on 100 % by weight of the pulp. In terms of the Kappa number, pulps suitable in the process of the invention are pulps having Kappa numbers up to 160, preferably in the range of 135 to 0, more preferably 100 to 0, most preferably 50 to 0.
  • Cationic dyes which can be used in the process of the invention are the cationic dyes as known from the prior art and as described above. In the present invention, "cationic dye" means, in line with the common understanding in the art, that the dye is derived from dye bases. Cationic dyes form positively charged ions (cations) by dissociation in water. The term "cationic dye" does not refer to the pH reaction of these dyes.
  • Suitable cationic dyes are the following cationic dyes, which are described according to the Color Index: Basic Blue 3, Basic Blue 26, Basic Blue 41, Basic Blue 54, Basic Blue 64, Basic Blue 100, Basic Blue 140, Basic Blue 159, Basic Blue 163, Basic Green 1, Basic Green 4, Basic Orange 1, Basic Orange 2, Basic Orange 21, Basic Orange 60, Basic Orange 64, Basic Orange 160, Basic Red 1, Basic Red 12, Basic Red 14, Basic Red 18, Basic Red 29, Basic Red 46, Basic Red 49, Basic Red 51, Basic Red 108, Basic Red 111, Basic Violet 1, Basic Violet 3, Basic Violet 4, Basic Violet 10, Basic Violet 14, Basic Violet 16, Basic Violet 49, Basic Yellow 1, Basic Yellow 11, Basic Yellow 13, Basic Yellow 15, Basic Yellow 21, Basic Yellow 28, Basic Yellow 29, Basic Yellow 40, Basic Yellow 51, Basic Yellow 70, Basic Yellow 94, Basic Yellow 96, Basic Brown 1, Basic Brown 22, and Basic Brown 23. Preferred cationic dyes are Basic Blue 159, Basic Blue 26, Basic Red 12, Basic Violet 16, Basic Red 49, Basic Violet 1, and Basic Yellow 90. The following cationic dyes which are indicated by their formulas are also preferred.
  • Basic Blue 159
  • Figure imgb0001
  • Basic Violet 1
  • Figure imgb0002
  • Basic Red 49
  • Figure imgb0003
  • Basic Yellow 90
  • Figure imgb0004
  • Basic Red 12
  • Figure imgb0005
  • Basic Violet 16
  • Figure imgb0006
  • Basic Green 1
  • Figure imgb0007
  • Basic Violet 3
  • Figure imgb0008
  • Basic Violet 4
  • Figure imgb0009
  • Basic Orange 2
  • Figure imgb0010
  • Basic Orange 21
  • Figure imgb0011
  • Basic Red 1
  • Figure imgb0012
  • Basic Red 46
  • Figure imgb0013
  • Basic Red 111
  • Figure imgb0014
  • Basic Yellow 11
  • Figure imgb0015
  • Basic Yellow 15
  • Figure imgb0016
  • Basic Yellow 21
  • Figure imgb0017
  • Basic Yellow 51
  • Figure imgb0018
  • Suitable amounts of cationic dye are within a range of 0.01 to 20 % by weight based on 100 % by weight of the pulp used. In a preferred embodiment of the invention, the cationic dye is used in an amount of 0.01 to 1 % by weight or in an amount of 0.05 to 10 % by weight, preferably 0.1 to 1 % by weight, more preferred 0.2 to 0.5 % by weight, based on 100 % by weight of the pulp. One or more cationic dyes can be used as a cationic dye.
  • The fluorescent whitening agents that can be used in the process of the invention are known fluorescent whitening agents and are subject to no limitations. Suitable fluorescent whitening agents are described in e.g. Klaus Hunger (Editor), Industrial Dyes, Wiley-VCH, Weinheim, 2003, Chapter 7.2, pages 590-610. In particular, fluorescent whitening agents having sulfonic acid residues are suitable. Preferably, there are used sulfonic acid groups-containing distyrylbenzenes, distyrylbiphenyls, divinylstilbenes, triazinylaminostilbenes, stilbenyl-2H-triazoles, stilbenyl-2H-naphtho[1,2-d]triazoles, bis(1,2,3-triazol-2-yl)stilbenes, benzoxazoles, stilbenylbenzoxazoles, bis-benzoxazoles, bis(benzo[b]furan-2-yl)biphenyls, benzimidazoles, 1,3-diphenyl-2-pyrazolines, coumarins, und naphthalimides.
  • Most preferably, the fluorescent whitening agent is a derivative of 4,4'-diaminostilbene-2,2'-disulfonic acid, in particular a 1,3,5-triazinyl derivative of 4,4'-diaminostilbene-2,2'-disulfonic acid or salts thereof. Most preferred are the disodium salt of 4,4'-bis[(4-anilino-6-diethanolamino-1,3,5-triazine-2-yl)amino]-stilbene-2,2'-disulfonic acid, the tetrasodium and hexasodium salt of 4,4'-bis[(4-p-sulfoanilino-6-diethanolamino-1,3,5-triazine-2-yl)amino]-stilbene-2,2'-disulfonic acid, and the hexasodium salt of 4,4'-bis[(4-(2,5-disulfoanilino)-6-diethanolamino-1,3,5-triazine-2-yl)amino]-stilbene-2,2'-disulfonic acid.
  • Suitable amounts of fluorescent whitening agent are within a range of 0.001 to 10 % by weight based on 100 % by weight of the pulp. In a preferred embodiment of the invention, the fluorescent whitening agent is used in an amount of 0.01 to 5 % by weight, preferably 0.1 to 1 % by weight, more preferably 0.2 to 0.4 % by weight, based on 100 % by weight of the pulp. As fluorescent whitening agent one or more fluorescent whitening agents can be used.
  • The process of the invention is carried out by adding the cationic dye to the pulp, and then adding the fluorescent whitening agent. The cationic dye and/or fluorescent whitening agent are suitably added by mixing or agitating. If the fluorescent whitening agent is added to the pulp with the added cationic dye too fast, a precipitate of fluorescent whitening agent and cationic dye is formed. Therefore, according to the invention the fluorescent whitening agent is suitably added to the pulp with the added cationic dye at a time at which no such precipitate is formed. This is usually after an agitation time in which the cationic dye has been sufficiently distributed in the pulp, and this depends on the agitation performance. Preferably, the fluorescent whitening agent is added some seconds or minutes, e.g. 30 seconds, or 1, 2, 3, 5, 10, 15 or 20 minutes, after the cationic dye has been added. In particular, the fluorescent whitening agent is added 5 to 10 minutes after the cationic dye addition. After that the paper sheet is formed.
  • It is preferred to add the cationic dye and/or fluorescent whitening agent by using a metering pump. The dye and/or fluorescent whitening agent can be added to the pulp in the paper machine in the pulper, in the mixing vat, in the stuff chest, before the headbox, or in the size press. The process of the invention can be carried out continuously, discontinuously (batch), or a combination of both by split dyeing. In the discontinuous process the dyeing is usually carried out batch wise in the pulper or the mixing vat. In the continuous process the dyeing is usually carried out by adding the dye and fluorescent whitening agent to the pulp stream. The dye and fluorescent whitening agent can be added in the thick matter area and/or thin (dilute) matter area. It is further possible to dye both in the pulp and on the surface. Surface dyeing or dipping can be carried out by using coating colours and e.g. a size press. It is possible to use coating colors with dye and fluorescent whitening agent. Further, it is possible to soak the base paper with dyeing solution and fluorescent whitening agent in a dipping tank, or to carry out a dyeing application in the plane using suitable printing procedures.
  • As shown by the following examples, the present invention surprisingly overcomes the problem that bleached wood-free pulp is insufficiently dyed by cationic dyes.
  • The following examples illustrate the invention without restricting its scope.
  • EXAMPLES
  • About 0.2 % by weight (based on 100 % by weight of pulp) of cationic dye is added to a bleached wood-free pulp containing about 2.5 % by weight of fibers, the remainder being mainly water. After an agitation period of 5 to 10 minutes a fluorescent whitening agent is added in an amount as indicated in the Tables below (the amount refers to % by weight based on 100 % by weight of the pulp). After 20 to 30 seconds the sheet is formed. The fluorescent whitening agent used is BLANKOPHOR DS, which contains the disodium salt of 4,4'-bis[(4-anilino-6-diethanolamino-1,3,5-triazine-2-yl)amino]-stilbene-2,2'-disulfonic acid.
  • COMPARATIVE EXAMPLES
  • In the comparative examples the anionic fixing agents MESITOL P, which is a commercial polycondensate of naphthalene sulfonic acid and formaldehyde, and MESITOL NBS, which is a commercial polycondensate of phenol sulfonic acid, 4,4'-dihydroxydiphenyl sulfone and formaldehyde, are used instead of the fluorescent whitening agent. Both fixing agents are present as sodium salts.
  • The % data hereinafter refer to percent by weight. The colour measurements are carried out with the CIELab system according to DIN 6174.
  • The following data have been measured:
    Sample L A B C
    ASTRA Blue B (Basic Blue 159) 81,88 -6,69 -14,59 16,05
    Addition of ΔL Δa Δb ΔC
    0,3% BLANKOPHOR DS -7,34 0,87 -15,13 14,24
    0,3% MESITOL NBS* -6,20 1,95 -7,20 6,25
    0,3% MESITOL P* 2,01 1,00 2,38 -2,58
    Sample L A B C
    ASTRA Brill. Red 4BC (Basic Red 49) 80,22 47,50 -12,04 49,00
    Addition of ΔL Δa Δb ΔC
    0,3% BLANKOPHOR DS -1,00 3,27 -11,76 7,07
    0,3% MESITOL NBS* -2,50 -11,64 -3,24 -10,02
    0,3% MESITOL P* 1,99 -7,24 1,33 -7,34
    Sample L A B C
    ASTRA Blue 6RL (Basic Violet 1) 62,93 16,61 -38,34 41,78
    Addition of ΔL Δa Δb ΔC
    0,3% BLANKOPHOR DS -1,90 3,92 -6,64 7,66
    0,3% MESITOL NBS* -6,09 5,68 -3,36 5,50
    0,3% MESITOL P* 9,39 -7,53 10,87 -12,85
    Sample L A B C
    ASTRA Yellow 4GN (Basic Yellow 90) 95,88 -6,90 19,51 20,69
    Addition of ΔL Δa Δb ΔC
    0,3% BLANKOPHOR DS 0,27 -3,39 7,97 8,65
    0,3% MESITOL NBS* -1,08 -1,87 14,21 4,15
    0,3% MESITOL P* -0,16 -0,24 2,67 2,61
    * Comparative sample
  • The higher ΔC is the more brilliant is the colour. The samples of the invention with fluorescent whitening agent exhibit higher ΔC values. Thus, in these samples the colour is more brilliant, compared to the comparative samples with the anionic fixing agents MESITOL, which result in less brilliant colourings.
  • Accordingly, dyeing bleached wood-free pulp with cationic dyes results in brilliant dyeing when using fluorescent whitening agents.

Claims (10)

  1. A process for dyeing pulp comprising bleached pulp, comprising adding at least one cationic dye to the pulp, and then adding at least one fluorescent whitening agent to the pulp, followed by forming the paper sheet.
  2. The process of claim 1, wherein a pulp containing at least 20 % by weight, preferably 50 to 100 % by weight, in particular 90 to 100 % by weight, of bleached pulp based on 100 % by weight of the pulp is used.
  3. The process of claim 1 or 2, wherein a wood-free pulp is used.
  4. The process of claim 1 or 2, wherein a pulp containing 0.1 to 50 % by weight, preferably 1 to 10 % by weight, of fibers based on 100 % by weight of the pulp is used.
  5. The process of claim 1 or 2, wherein a pulp having a Kappa number up to 160, in particular a Kappa number in the range of 100 to 0, is used.
  6. The process of any of the preceding claims, wherein the cationic dye is added in an amount of 0.01 to 20 % by weight, preferably 0.01 to 1 % by weight, based on 100 % by weight of the pulp.
  7. The process of any of the preceding claims, wherein the cationic dye is selected from Basic Blue 26, Basic Blue 159, Basic Red 12, Basic Red 49, Basic Violet 1, Basic Violet 16, and Basic Yellow 90.
  8. The process of any of the preceding claims, wherein the fluorescent whitening agent is added in an amount of 0.001 to 10 % by weight, preferably 0.1 to 1 % by weight, based on 100 % by weight of the pulp.
  9. The process of any of the preceding claims, wherein the fluorescent whitening agent is derived from 4,4'-diaminostilbene-2,2'-disulfonic acid, in particular wherein the whitening fluorescent agent is a 1,3,5-triazinyl derivative of 4,4'-diaminostilbene-2,2'-disulfonic acid.
  10. Paper obtainable by a process according to any of the preceding claims.
EP09163790A 2009-06-25 2009-06-25 Process for dyeing pulp Withdrawn EP2270281A1 (en)

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EP09163790A EP2270281A1 (en) 2009-06-25 2009-06-25 Process for dyeing pulp
PCT/EP2010/059070 WO2010149773A1 (en) 2009-06-25 2010-06-25 Process for dyeing pulp

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4198197A1 (en) * 2021-12-20 2023-06-21 Mondi AG Method for producing a multi-layer packaging paper or board

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106280544B (en) * 2015-05-29 2017-11-17 上海汇友精密化学品有限公司 A kind of cationic black dyes composition
CN112903105A (en) * 2021-01-15 2021-06-04 金发科技股份有限公司 Method for measuring color fluorescence intensity and fluorescence color of material

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3742012A (en) * 1972-01-13 1973-06-26 Du Pont Quaternary styryl dyestuffs
US4374643A (en) 1980-07-22 1983-02-22 Showa Kagaku Kogyo Co., Ltd Color salts of basic dyes with acidic optical brighteners of stilbene type
US4540523A (en) * 1977-04-01 1985-09-10 Bayer Aktiengesellschaft Phenylalkylamino-styryl dyestuffs
EP0899373A1 (en) * 1997-08-28 1999-03-03 Ciba SC Holding AG Method of whitening lignin-containing pulp during manufacture
WO2007104128A1 (en) * 2006-03-13 2007-09-20 Fp Innovations Near-neutral chlorine dioxide bleaching of pulp

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3742012A (en) * 1972-01-13 1973-06-26 Du Pont Quaternary styryl dyestuffs
US4540523A (en) * 1977-04-01 1985-09-10 Bayer Aktiengesellschaft Phenylalkylamino-styryl dyestuffs
US4374643A (en) 1980-07-22 1983-02-22 Showa Kagaku Kogyo Co., Ltd Color salts of basic dyes with acidic optical brighteners of stilbene type
EP0899373A1 (en) * 1997-08-28 1999-03-03 Ciba SC Holding AG Method of whitening lignin-containing pulp during manufacture
WO2007104128A1 (en) * 2006-03-13 2007-09-20 Fp Innovations Near-neutral chlorine dioxide bleaching of pulp

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
"Industrial Dyes", 2003, WILEY-VCH
"Industrial Dyes", 2003, WILEY-VCH, pages: 460
"Industrial Dyes", 2003, WILEY-VCH, pages: 590 - 610
J. S. GRATZL: "Chemische Grundlagen der Zellstoffbleiche mit Sau- erstofj; Wasserstoffperoxid und Ozon", DAS PAPIER, vol. 46, no. 10A, 1992, pages VL - V8
M. J. KOCUREK: "Joint textbook Committee of the Paper Industry", vol. 1, 1983, TAPPI CPPA, article "Pulp and Paper Manufacture"
P. RYS; H. ZOLLINGER: "Fundamentals of the Chemistry and Application of Dyes", 1972, WILEY INTERSCIENCE

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4198197A1 (en) * 2021-12-20 2023-06-21 Mondi AG Method for producing a multi-layer packaging paper or board

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