EP0227623B1 - Use of alkylamine salts as viscosity regulating substance - Google Patents

Use of alkylamine salts as viscosity regulating substance Download PDF

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Publication number
EP0227623B1
EP0227623B1 EP86850427A EP86850427A EP0227623B1 EP 0227623 B1 EP0227623 B1 EP 0227623B1 EP 86850427 A EP86850427 A EP 86850427A EP 86850427 A EP86850427 A EP 86850427A EP 0227623 B1 EP0227623 B1 EP 0227623B1
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EP
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Prior art keywords
alkyl amine
use according
alkyl
mix
coating
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EP86850427A
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German (de)
French (fr)
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EP0227623A1 (en
Inventor
Sverker HÖGBERG
Rolf Sigurdsson
Viveka Svensson
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Kemira Kemi AB
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Kemira Kemi AB
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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
    • D21H19/00Coated paper; Coating material
    • D21H19/36Coatings with pigments
    • D21H19/44Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
    • D21H19/46Non-macromolecular organic compounds
    • 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
    • D21H19/00Coated paper; Coating material
    • D21H19/36Coatings with pigments
    • D21H19/38Coatings with pigments characterised by the pigments
    • D21H19/385Oxides, hydroxides or carbonates
    • 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
    • D21H19/00Coated paper; Coating material
    • D21H19/36Coatings with pigments
    • D21H19/38Coatings with pigments characterised by the pigments
    • D21H19/40Coatings with pigments characterised by the pigments siliceous, e.g. clays

Definitions

  • the present invention relates to the use of acid addition salts of alkyl amines for regulating the viscosity of paper coating mixes when blending such mixes.
  • the object of the present invention is to enable the interchange of coating mixes in continuous paper coating processes without substantial change in the viscosity of said mixes at the transition from one mix to the other and/or the mixing of the mixes one with the other.
  • Paper is coated by applying an extremely thin layer of coating mix to a paper web.
  • the purpose of the coating is to improve the properties of the paper, particularly with regard to uniformity of surface, and its ability to accept inks, lacquers etc. from the printing press.
  • Such mixes today comprise finely ground kaolin, dispersant, and water, or chalk, dispersant, water.
  • Mixes have also been proposed, and prepared that comprises calcium sulphate dihydrate (gypsum), dispersant and water. It has also been found, however, that when switching from a gypsum mix to a kaolin mix the viscosity of the combined mixes is much higher than that of a single mix, which renders the system inoperable.
  • DE-A1-1 696 193 discloses the use of polyvinylalcohol as a binding agent in satin white-based coating mixtures, whereby an amine, alkali or ammoniumsalt of a polycarboxylic acid is used as an impart useable viscosity to the formulation.
  • the polycarboxylic acids used are particularly those being of high molecular weight, such as sodium polyacrylate, sodium polyvinyl sulphonate, and sodium carboxy methyl cellulose.
  • EP-A2-0 004 062 discloses aqueous dispersions of polymers, particularly on the basis of vinylpolymers, whereby salts of primary, secondary and tertiary aliphatic amines are used as dispersing agents.
  • the acid addition salt is prepared by reaction with sulphuric acid, phosphoric acid, hydrochloric acid, nitric acid, perchloric acid, aliphatic, alicyclic, aromatic and heterocyclic carboxylic and sulphonic acids.
  • such salts are hydrochlorides, sulphate, hydrogen sulphate, phosphate, hydrogen phosphate, nitrate, formiate, acetate, propionate, succinate, glycolate, gluconate, heptonate, lactate, tartrate, citrate, oxalate, ascorbate, maleate, hydroxy maleate, bensoate, p-amino bensoate, p-hydroxy bensoate, salicylate, p-amino salicylate, picrate, diethylene triamine pentaacetate (DTPA), ethylene diamine tetraacetate (EDTA), nitrilo triacetate (NTA), hydroxy ethyl imino diacetate, bis(hydroxyethyl)gluconate.
  • DTPA diethylene triamine pentaacetate
  • EDTA ethylene diamine tetraacetate
  • NTA nitrilo triacetate
  • the alkyl amines used in the group preferably comprise primary alkyl amines, such as methyl amine, ethyl amine, propyl amine, 1-methyl ethyl amine, butyl amine, 1-methyl propyl amine, 2-methyl propyl amine, pentyl amine, 3-methyl butyl amine, 2-methyl butyl amine, 1-ethyl propyl amine, 1-methyl butyl amine, 1,1-dimethyl ethyl amine, 1,1-dimethyl propyl amine, although they may also comprise secondary, tertiary and quarternary alkyl amines, such as dimethyl amine, diethyl amine, triethyl amine, tetramethyl amine.
  • primary alkyl amines such as methyl amine, ethyl amine, propyl amine, 1-methyl ethyl amine, butyl amine, 1-methyl propyl amine, 2-methyl propy
  • the product is prepared by mixing a solution of an alkyl amine with a solution of an acid which will react to form the intended acid addition salt. It is irrelevant in this respect whether one solution is added to the other, or vice versa.
  • the respective solutions may have the form of a concentrate or a solvent solution of the compound concerned.
  • the ratio of amine to acid is from 1 to 4, depending upon the degree of substitution desired.
  • the reaction between alkyl amine and acid takes place instantaneously, whereafter the product can be filtered off (when the reaction takes place in a non-dissolving solvent) or can be used direct, in solution.
  • a further gypsum based mix was prepared from 100 parts dry gypsum, 1.5 parts CMC, 9 parts latex DOW 685, NaOH to pH 8.5 and water, there being obtained a mix with DS 64.4%, viscosity 950 cps.
  • Various amines according to the aforegoing were added to 400 g of the kaolin mix thus prepared, in the quantities set forth in Table 1, whereafter 30.1 g of the gypsum mix were added and the viscosity of the resultant mixture was measured. The viscosity was also measured after adding the amine.
  • the results obtained when adding the gypsum based mix are set forth in the right column of Table 1 below.
  • the present invention has also been tested on a semi-industrial scale in an apparatus having a volume of 25 litres.
  • the apparatus comprised a machine tank having a volumetric filling capacity of 15 litres, a filter, and a buffer tank provided with an outlet leading to the machine tank and to the "coating station", i.e. the apparatus simulated the coating of a paper web by taking out 1 litre of mix per minute.
  • the volume circulated was 7 litres and the flow rate 10 litres per minute.
  • the system was filled with a mix 1. Whereafter the mix was pumped around the system, and "coating commenced".
  • Table 2 The results set forth in Table 2 were obtained when testing a conventional kaolin coating mix (mix 2), 100 parts of kaolin, 0.35 parts Dispex R N40, -'1.2 parts of CMC FFS, and 9 parts of latex DOW 685, DS 56-59%, pH 8.5-9, and a gypsum-based coating mix (mix 1) comprising 100 parts of dry gypsum dihydrate, 1.5 parts of CMC, and 9 parts of DOW 685, DS 60-65%, pH 8.5-9, without further addition of a compound according to the present invention.
  • a conventional kaolin coating mix (mix 2), 100 parts of kaolin, 0.35 parts Dispex R N40, -'1.2 parts of CMC FFS, and 9 parts of latex DOW 685, DS 56-59%, pH 8.5-9
  • a gypsum-based coating mix (mix 1) comprising 100 parts of dry gypsum dihydrate, 1.5 parts of CMC, and 9 parts of DOW 685, DS 60
  • Table 3 discloses the results obtained when adding to mix 1 (the gypsum mix) 0.4 parts of propyl amine phosphate, calculated as amine.
  • kaolin-based mix By kaolin-based mix is meant-here and in the aforegoing, a mix in which the pigment fraction contains more than 50% kaolin. Kaolin mixes that contain 60% kaolin and 40% gypsum are thus known in the art.
  • chalk-based mixes is meant a mix that contains more than 50% chalk
  • gypsum-based mixes is meant a mix that contains more than 50% gypsum.
  • the pigment fraction need not be totally based on one pigment.
  • DS means dry substance
  • Dow Latex is a polymer, whereby Dow Latex 685 is a carboxylated styrene-butadiene
  • DISPEX R N40 is a sodium salt of polycarboxylic acid
  • CMC is carboxymethyl cellulose, where CMC FF5 has an extra low viscosity level determined to 35-55 mPa - s at 25°C and a concentration of 4% dry matter.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Paper (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Radiation-Therapy Devices (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Paints Or Removers (AREA)

Abstract

The present invention relates to novel compounds in the form of alkyl amine acid addition salts, which compounds have the ability to regulate the viscosity of coating mixes when mixing together mixes of mutually different basic compositions. The invention also relates to the use of such alkyl amine acid addition salts for controlling the viscosity of a combined mixture of such coating mixes.

Description

    Technical field
  • The present invention relates to the use of acid addition salts of alkyl amines for regulating the viscosity of paper coating mixes when blending such mixes.
  • The object of the present invention is to enable the interchange of coating mixes in continuous paper coating processes without substantial change in the viscosity of said mixes at the transition from one mix to the other and/or the mixing of the mixes one with the other.
  • Background of the invention
  • Paper is coated by applying an extremely thin layer of coating mix to a paper web. The purpose of the coating is to improve the properties of the paper, particularly with regard to uniformity of surface, and its ability to accept inks, lacquers etc. from the printing press. Such mixes today comprise finely ground kaolin, dispersant, and water, or chalk, dispersant, water. Mixes have also been proposed, and prepared that comprises calcium sulphate dihydrate (gypsum), dispersant and water. It has also been found, however, that when switching from a gypsum mix to a kaolin mix the viscosity of the combined mixes is much higher than that of a single mix, which renders the system inoperable.
  • Due to the complexity of paper machines it is not convenient to stop production in order to clean the coating equipment. It is also necessary, however, to be able to switch from one type of mix to another without stopping production in order to satisfy demands for paper with different coatings.
  • Various systems have been tested, inter alia with variation of the dispersant, although without success.
  • DE-A1-1 696 193 discloses the use of polyvinylalcohol as a binding agent in satin white-based coating mixtures, whereby an amine, alkali or ammoniumsalt of a polycarboxylic acid is used as an impart useable viscosity to the formulation. The polycarboxylic acids used are particularly those being of high molecular weight, such as sodium polyacrylate, sodium polyvinyl sulphonate, and sodium carboxy methyl cellulose.
  • EP-A2-0 004 062 discloses aqueous dispersions of polymers, particularly on the basis of vinylpolymers, whereby salts of primary, secondary and tertiary aliphatic amines are used as dispersing agents.
  • Summary of the invention
  • It has now surprisingly been found possible to solve this problem in a simple and efficient manner by means of the present invention which to this end proposes the use of compounds which comprise an acid addition salt of an alkyl amine having 1-5 carbon atoms in the alkyl chain, preferably 2-4 carbon atoms and still more preferably 3-4 carbon atoms.
  • Part of the alkyl amine is present as an acid addition salt. The acid addition salt is prepared by reaction with sulphuric acid, phosphoric acid, hydrochloric acid, nitric acid, perchloric acid, aliphatic, alicyclic, aromatic and heterocyclic carboxylic and sulphonic acids. In this regard, such salts are hydrochlorides, sulphate, hydrogen sulphate, phosphate, hydrogen phosphate, nitrate, formiate, acetate, propionate, succinate, glycolate, gluconate, heptonate, lactate, tartrate, citrate, oxalate, ascorbate, maleate, hydroxy maleate, bensoate, p-amino bensoate, p-hydroxy bensoate, salicylate, p-amino salicylate, picrate, diethylene triamine pentaacetate (DTPA), ethylene diamine tetraacetate (EDTA), nitrilo triacetate (NTA), hydroxy ethyl imino diacetate, bis(hydroxyethyl)gluconate.
  • Further characteristics are set forth in the following claims.
  • The alkyl amines used in the group preferably comprise primary alkyl amines, such as methyl amine, ethyl amine, propyl amine, 1-methyl ethyl amine, butyl amine, 1-methyl propyl amine, 2-methyl propyl amine, pentyl amine, 3-methyl butyl amine, 2-methyl butyl amine, 1-ethyl propyl amine, 1-methyl butyl amine, 1,1-dimethyl ethyl amine, 1,1-dimethyl propyl amine, although they may also comprise secondary, tertiary and quarternary alkyl amines, such as dimethyl amine, diethyl amine, triethyl amine, tetramethyl amine.
  • The product is prepared by mixing a solution of an alkyl amine with a solution of an acid which will react to form the intended acid addition salt. It is irrelevant in this respect whether one solution is added to the other, or vice versa.
  • The respective solutions may have the form of a concentrate or a solvent solution of the compound concerned.
  • The ratio of amine to acid is from 1 to 4, depending upon the degree of substitution desired.
  • In the process of adding one solution to the other, care is taken to ensure that the alkyl amine does not boil, by a suitable control of temperature.
  • The reaction between alkyl amine and acid takes place instantaneously, whereafter the product can be filtered off (when the reaction takes place in a non-dissolving solvent) or can be used direct, in solution.
  • Example 1
  • 33.6 kg of citric monohydrate were dissolved in 30 I of water. 36 I (25.9 kg) of n-propyl amine were then added carefully to the solution, while stirring and cooling the system. The temperature was maintained beneath 45°C. The resultant product, (n-propylamine)3-citrate remained in solution in the water phase.
  • The following systems were.prepared in a similar manner:
  • Figure imgb0001
  • A series of experiments was conducted on the basis of the above substances, in which there was prepared a first kaolin mix comprising 100 parts of dry kaolin, 50 parts of water, 0.35 parts of 100%-DispexR and NaOH. The pH of the mix was 8.5. A suspension was then prepared over a period of one hour, by adding to the mix 9 parts of DOW 685,1.2 parts of CMC (carboxy methyl cellulose) and water to a viscosity of about 1500 cps, dry solids (DS) content 55­58%. Peripheral data concerning different starting kaolin mixes is given in Table 1 below, left column.
  • A further gypsum based mix was prepared from 100 parts dry gypsum, 1.5 parts CMC, 9 parts latex DOW 685, NaOH to pH 8.5 and water, there being obtained a mix with DS 64.4%, viscosity 950 cps. Various amines according to the aforegoing were added to 400 g of the kaolin mix thus prepared, in the quantities set forth in Table 1, whereafter 30.1 g of the gypsum mix were added and the viscosity of the resultant mixture was measured. The viscosity was also measured after adding the amine. The results obtained when adding the gypsum based mix are set forth in the right column of Table 1 below.
    Figure imgb0002
  • The present invention has also been tested on a semi-industrial scale in an apparatus having a volume of 25 litres. The apparatus comprised a machine tank having a volumetric filling capacity of 15 litres, a filter, and a buffer tank provided with an outlet leading to the machine tank and to the "coating station", i.e. the apparatus simulated the coating of a paper web by taking out 1 litre of mix per minute. The volume circulated was 7 litres and the flow rate 10 litres per minute. The system was filled with a mix 1. Whereafter the mix was pumped around the system, and "coating commenced". Subsequent to emptying the machine tank, by consecutive simulated "coating" procedures, such that about 10 litres of mix 1 remained, the system was refilled with mix 2, this mix being intended to replace mix 1 without interrupting circulation and while continuing the "coating" process. Samples were taken from the combined mixture of mixes 1 and 2 at 30 second intervals, in order to determine the viscosity, pH, and in some cases also DS and the ratio of mix 1 to mix 2 in the combined coating mixture.
  • The results set forth in Table 2 were obtained when testing a conventional kaolin coating mix (mix 2), 100 parts of kaolin, 0.35 parts DispexR N40, -'1.2 parts of CMC FFS, and 9 parts of latex DOW 685, DS 56-59%, pH 8.5-9, and a gypsum-based coating mix (mix 1) comprising 100 parts of dry gypsum dihydrate, 1.5 parts of CMC, and 9 parts of DOW 685, DS 60-65%, pH 8.5-9, without further addition of a compound according to the present invention.
    Figure imgb0003
  • Table 3 below discloses the results obtained when adding to mix 1 (the gypsum mix) 0.4 parts of propyl amine phosphate, calculated as amine.
    Figure imgb0004
  • In a further test, mix 1 and mix 2 were mixed together in different proportions, while carefully stirring the system for one minute. The viscosity of the combined mixture was determined in accordance with the Brookfield technique (30 s 100 rpm). In this test, a study was made of a mixture between a gypsum-based mix according to the above (mix 1) and a kaolin mix (mix 2) with a synthetic thickener, DS 55% and Viscosity mPas. The results are given in Tables 4 and 5 below.
    Figure imgb0005
  • It is evident from the above that the viscosity of the coating mixture is stabilized very effectively when an alkyl amine acid addition salt according to the aforesaid is used.
  • It has been found that when using the alkyl amine acid addition salt, an acceptable result is achieved even when only a part of the alkyl amine exists in the form of such an acid addition salt.
  • A satisfactory result can also be obtained by adding each of the salt components, i.e. alkyl amine and acid, separately, to the coating mix.
  • By kaolin-based mix is meant-here and in the aforegoing, a mix in which the pigment fraction contains more than 50% kaolin. Kaolin mixes that contain 60% kaolin and 40% gypsum are thus known in the art.
  • By chalk-based mixes is meant a mix that contains more than 50% chalk, while by gypsum-based mixes is meant a mix that contains more than 50% gypsum. Thus the pigment fraction need not be totally based on one pigment.
  • In the above the abbreviation DS means dry substance; Dow Latex is a polymer, whereby Dow Latex 685 is a carboxylated styrene-butadiene; DISPEXR N40 is a sodium salt of polycarboxylic acid; CMC is carboxymethyl cellulose, where CMC FF5 has an extra low viscosity level determined to 35-55 mPa - s at 25°C and a concentration of 4% dry matter.

Claims (11)

1. The use of an acid addition salt of an alkyl amine having 1 to 5 carbon atoms in the alkyl chain for regulating the viscosity of paper coating mixes when blending together different kinds of such mixes, whereby the acid addition salt is a hydrochloride, hydrogen sulphate, hydrogen phosphate, sulphate, phosphate, nitrate, formiate, acetate, propionate, succinate, glycolate, heptonate, lactate, tartrate, citrate, oxalate, ascorbate, maleate, hydroxy maleate, bensoate, p-aminobensoate, p-hydroxy bensoate, salicylate, p-aminosalicylate, picrate, diethylene triamine pentaacetate, ethylene diamine tetraacetate, nitrilo triacetate, hydroxy ethyleneiminodiacetate, and bis-(hydroxyethyl)gluconate.
2. The use according to claim 1, wherein the compound is added in an amount corresponding to 0.05 to 2% by weight of the weight of the ingoing prepared coating mixture.
3. The use according to claim 1, wherein the coating mixtures consist respectively of a kaolin-based and a calcium sulphate-based coating mix.
4. The use according to claim 1, wherein the coating mixes consist respectively of a chalk-based and a calcium sulphate-based coating mix.
5. The use according to claim 1, wherein the coating mixes consist respectively of a kaolin-based and a chalk-based coating mix.
6. The use according to claims 1-5, wherein the alkyl amine has 2 to 4 carbon atoms in the alkyl chain.
7. The use according to claim 6, wherein the alkyl amine has 3 to 4 carbon atoms in the alkyl chain.
8. The use according to claims 1-5, wherein the alkyl amine is a primary alkyl amine.
9. The use according to claims 1-5, wherein the alkyl amine is a secondary alkyl amine.
10. The use according to claims 1-5, wherein the alkyl amine is a tertiary alkyl amine having 1 to 3 carbon atoms in the alkyl groups.
11. The use according to claim 1, wherein the alkyl amine is a quaternary alkyl amine having 1 to 2 C in the alkyl groups.
EP86850427A 1985-12-09 1986-12-08 Use of alkylamine salts as viscosity regulating substance Expired - Lifetime EP0227623B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT86850427T ATE55107T1 (en) 1985-12-09 1986-12-08 USE OF ALKYLAMINE SALTS AS VISCOSITY REGULATOR.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE8505811 1985-12-09
SE8505811A SE451470B (en) 1985-12-09 1985-12-09 APPLICATION OF AN ACID ADDITION SALT OF AN ALKYLAMINE FOR REGULATING THE VISCOSITY OF PAPER COATING METHODS

Publications (2)

Publication Number Publication Date
EP0227623A1 EP0227623A1 (en) 1987-07-01
EP0227623B1 true EP0227623B1 (en) 1990-08-01

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EP86850427A Expired - Lifetime EP0227623B1 (en) 1985-12-09 1986-12-08 Use of alkylamine salts as viscosity regulating substance

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AT (1) ATE55107T1 (en)
DE (1) DE3673144D1 (en)
ES (1) ES2016568B3 (en)
FI (1) FI864771A7 (en)
SE (1) SE451470B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8252143B2 (en) 2004-06-22 2012-08-28 Akzo Nobel N.V. Filler for paper making process

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL1778916T3 (en) * 2004-06-22 2016-10-31 Filler for paper making process

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1150561A (en) * 1965-07-14 1969-04-30 Kurashiki Rayon Kk Coating Compositions for High Grade Paper
DE1696193B2 (en) * 1966-04-07 1974-07-04 Farbwerke Hoechst Ag, Vormals Meister Lucius & Bruening, 6000 Frankfurt Satin white coating slips with good viscosity stability
DE2810348A1 (en) * 1978-03-10 1979-09-20 Hoechst Ag AQUEOUS PLASTIC DISPERSION BASED ON VINYL POLYMERS

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, vol. 25, no. 1, Jan 1931; A.NYSSENS: " The identification of aliphatic amines", pp. 69-70 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8252143B2 (en) 2004-06-22 2012-08-28 Akzo Nobel N.V. Filler for paper making process
US8828188B2 (en) 2004-06-22 2014-09-09 Akzo Nobel N.V. Filler for paper making process
US9657441B2 (en) 2004-06-22 2017-05-23 Akzo Nobel N.V. Filler for paper making process

Also Published As

Publication number Publication date
ATE55107T1 (en) 1990-08-15
FI864771A0 (en) 1986-11-24
SE8505811D0 (en) 1985-12-09
FI864771L (en) 1987-06-10
SE451470B (en) 1987-10-12
EP0227623A1 (en) 1987-07-01
ES2016568B3 (en) 1990-11-16
DE3673144D1 (en) 1990-09-06
FI864771A7 (en) 1987-06-10
SE8505811L (en) 1987-06-10

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