EP0413736B1 - Method of making mechanical and chemi-mechanical papermaking pulp - Google Patents

Method of making mechanical and chemi-mechanical papermaking pulp Download PDF

Info

Publication number
EP0413736B1
EP0413736B1 EP19890905472 EP89905472A EP0413736B1 EP 0413736 B1 EP0413736 B1 EP 0413736B1 EP 19890905472 EP19890905472 EP 19890905472 EP 89905472 A EP89905472 A EP 89905472A EP 0413736 B1 EP0413736 B1 EP 0413736B1
Authority
EP
European Patent Office
Prior art keywords
pulp
ton
kwh
beating
energy consumption
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.)
Expired - Lifetime
Application number
EP19890905472
Other languages
German (de)
French (fr)
Other versions
EP0413736A1 (en
Inventor
Per Ossian Engstrand
Lars-Ake Hammar
Myat Thoung Htun
Rune Lennart Pettersson
Börje Nils SVENSSON
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.)
STFI Skogsindustrins Tekniska Forskningsinstitut AB
Original Assignee
STFI Skogsindustrins Tekniska Forskningsinstitut AB
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 STFI Skogsindustrins Tekniska Forskningsinstitut AB filed Critical STFI Skogsindustrins Tekniska Forskningsinstitut AB
Priority to AT89905472T priority Critical patent/ATE94596T1/en
Publication of EP0413736A1 publication Critical patent/EP0413736A1/en
Application granted granted Critical
Publication of EP0413736B1 publication Critical patent/EP0413736B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21BFIBROUS RAW MATERIALS OR THEIR MECHANICAL TREATMENT
    • D21B1/00Fibrous raw materials or their mechanical treatment
    • D21B1/04Fibrous raw materials or their mechanical treatment by dividing raw materials into small particles, e.g. fibres
    • D21B1/12Fibrous raw materials or their mechanical treatment by dividing raw materials into small particles, e.g. fibres by wet methods, by the use of steam
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21BFIBROUS RAW MATERIALS OR THEIR MECHANICAL TREATMENT
    • D21B1/00Fibrous raw materials or their mechanical treatment
    • D21B1/04Fibrous raw materials or their mechanical treatment by dividing raw materials into small particles, e.g. fibres
    • D21B1/12Fibrous raw materials or their mechanical treatment by dividing raw materials into small particles, e.g. fibres by wet methods, by the use of steam
    • D21B1/14Disintegrating in mills
    • D21B1/16Disintegrating in mills in the presence of chemical agents

Definitions

  • This invention relates to a method of making mechanical and chemi-mechanical papermaking pulp by disintegrating and beating wood material in at least two steps.
  • One object of the invention is to carry out the disintegration and beating in such a manner, that the total energy consumption is substantially reduced, as will be be described in the following.
  • the beating of cellulose-containing material at low pulp concentration is a method, which has been employed since long in order to improve the paperforming properties of the fibres. This applies, however, only to fibres free of lignin or substantially free of lignin, such as fibres produced according to the sulphate or sulphite method.
  • pulps manufactured mechanically such as thermomechanical pulp (TMP) or chemi-mechanical pulp (CTMP)
  • TMP thermomechanical pulp
  • CMP chemi-mechanical pulp
  • beating at low concentration so-called post-refining, was not considered applicable other than as a method for increasing the light-scattering capacity of the pulps and for reducing slightly the fibre length and thereby improving the formation at the making of paper.
  • thermomechanical pulp with fibre-modifying chemicals Experiments have been carried out previously to treat thermomechanical pulp with fibre-modifying chemicals. It was then found, that by treating the defibered pulp with ozone prior to the refining in a two-step process the energy consumption could be lowered by up to 30%. This, however, could be achieved only at the expense of the yield.
  • the wood material in a first step is coarse-disintegrated at a concentration of above 20%.
  • the energy input here shall be at maximum 8oo kWh/ton wood material.
  • the acid groups included in the wood material thereafter shall be neutralized entirely or partially, and the material be diluted with water of a temperature corresponding to the softening temperature of the lignin.
  • the dilution water shall have an ion strength of at maximum 0.05 mole per litre.
  • the coarse-disintegrated material then shall be beaten at a concentration of 1-10% with an energy input of totally a maximum of 500 kWh/ton material.
  • the present invention is based on the idea that there is a relation between the disintegration of the wood material to fibres and the way, in which the energy pulses are transferred to the material, i.e. whether the energy pulses are transferred in liquid phase or steam phase. Attention also is to be paid to the thermal and physical state of the wood material when the energy pulses are being transferred.
  • the energy input in the first coarse-defibering step must be low.
  • the first high concentration step can be at atmospheric pressure or pressurized and be carried out by tearing (shredding), chip pressing, plug screwing (type Impressafiner or PREX) or by defibering in a refiner.
  • the final beating then takes place in one or several steps at low pulp concentration, i.e. at a concentration of 1-10%.
  • the specific edge load is sufficiently low, and that the temperature and chemical environment of the fibre suspension has been adjusted to the softening and swelling state of the wood polymers.
  • the temperature at the beating shall be at least as high as the softening temperature of the stiffest amorphous wood polymer, that the acid groups of the wood polymers substantially are ionized, and that the ion strength of the process water is sufficiently low.
  • the flow sheet according to Fig. 1 illustrates the manufacture of thermomechanical pulp for newsprint.
  • Chips from spruce were steamed in a first step and preheated.
  • the preheated chips then were disintegrated in a pressurized refiner with an energy consumption of 700 kWh/ton.
  • 3 kg NaOh were added in the beating zone of the refiner for neutralizing acid groups included in the wood material.
  • To the defibered material dilution water with a temperature of 80 o C and an ion strength of 2.0 mmole/l was added in order to obtain a pulp concentration of 3%.
  • the pulp then was beaten in five subsequent steps at a specific edge load of 0.3-0.5 ws/m and a total net energy consumption of 150 kWh/ton pulp corresponding to a gross energy consumption of 250 kWh/ton pulp to a freeness of 150 ml CSF and a mean fibre length (PML) of 1.8 mm, i.e. about equal to TMP-pulp manufactured in conventional manner with an energy consumption of 1750 kWh/ton pulp.
  • PML mean fibre length
  • the total energy consumption at the method according to the invention thus, was reduced from 1750 to 950 kWh/ton pulp.
  • TMP The manufacture of TMP according to the invention is compared in Fig. 2, 3 and 4 with TMP manufactured conventionally with single-step refining in twin-disc refiner, which is the least energy consuming TMP-process existing with the present state of art.
  • Fig. 2 shows the tensile index as a function of the electric energy consumption. It appears clearly from the Figure, that the increase in tensile index at a certain electric energy consumption is considerably greater for TMP manufactured according to the invention.
  • Fig. 3 shows the tear index as a function of the tensile index for TMP according to the invention and conventional TMP. It appears that the development of the tear index for the respective TMP is about the same, i.e. at optimation of the low concentration beating according to the invention the fibre cutting and thereby the serious decrease in tear index are substantially entirely avoided, which cutting and decrease occur usually at conventional low concentration beating of mechanical pulps.
  • Fig. 4 shows how the light-scattering coefficient (s) develops at conventional TMP and TMP manufactured according to the invention. It appears that the s-development requires as low an electric energy input as the tensile index development, i.e. the saving of electric energy to a certain s-value is of equal size as the saving of electric energy to a certain tensile index value.
  • This example relates to the manufacture of chemi-mechanical pulp (CTMP or CMP) according to the flow sheet shown in Fig. 5.
  • CMP chemi-mechanical pulp
  • impregnation chemicals which can be sulphites, peroxide, oxygen gas, ozone and/or liquor, can take place prior to the first defibering step, after this step but prior to the final beating, after the final beating, or at combinations of these. In the flow sheet shown the impregnation is carried out prior to the first defibering step.
  • the first defibering step at high concentration is carried out in the same way as in Example 1.
  • the washing step is very essential, so that according to the invention the beating shall take place at low ion strength.
  • the washing therefore, is carried out prior to the final beating. In cases when the chemical treatment is carried out as the last process step, washing takes place even after this step.
  • the final beating takes place in the same way as according to Example 1, but process temperature and chemical environment must be adjusted to the special properties, which the wood polymers have assumed by treatment with impregnation chemicals. It is essential to pay regard to the number of sulphonic acid groups, which have been introduced by possible sulphite treatment. As an increasing amount of sulphonic acid groups reduces the softening temperature of the lignin, the temperature of the process water can be lower than at the manufacture of TMP-pulp according to Example 1. A sufficiently high temperature at the manufacture of CTMP is 40 o C. From a brightness point of view it is advantageous to use the lowest possible temperature. By sodium sulphite treatment both the sulphonic acid groups and the carboxylic acid groups ate ionized from the beginning.
  • the pulp then was beaten with a specific edge load of 0.3-0.5 Ws/m in five subsequent steps with a net energy consumption of 150 kWh/ton corresponding to a gross energy consumption of 250 kWh/ton for obtaining a pulp with a freeness of 250 ml CSF and a mean fibre length (PML) of 1.7 mm, i.e. as a conventionally manufactured CTMP-pulp produced in one step with an energy consumption of 1750 kWh/ton.
  • PML mean fibre length
  • the energy consumption was reduced from the conventional 1750 kWh/ton to 850 kWh/ton.
  • CTMP-pulp obtained compared with conventional CTMP-pulp are shown in Table 2.
  • Table 2 Conventional Invention Energy consumption,kWh/ton 1750 850 CSF ml 250 250 PML, mm - 1.7 Tensile index, kNm/kg 40 40 Tensile stiffness index - 4.6 Stretch at break, % 1.9 1.6 Tear index Nm2/kg 6.7 5.5 Density, kg/m3 420 450 S, m2/kg 43 45 ISO-brightness, % 60 60
  • tensile index is shown as a function of the energy consumption for a CTMP-pulp manufactured according to the invention and for pulp manufactured conventionally. Compared at a certain tensile index, for example 40 kNm/kg, conventional refining consumes about 1750 kWh/ton pulp while at the method according to the invention only about 850 kWh/ton are consumed.
  • the light-scattering coefficient of the CTMP-pulp manufactured according to the invention as a function of the energy consumption is shown in the diagram in Fig. 8 compared with conventionally manufactured pulp. It shows here that according to the invention the energy consumption to a certain light-scattering index is substantially lower.
  • This example relates to the manufacture of highly sulfonated CTMP or CMP, i.e pulp containing more than 4 g of bound sulphur per kg wood material.
  • Chips from spruce were impregnated with a sodium sulphite solution containing about 120 g of sodium sulphite per litre in an amount corresponding to a charge of about 12%.
  • the chips were preheated at a temperature of 140 o C for 10 minutes, whereafter they were coarse-disintegrated with an energy consumption of about 400 kWh/ton wood.
  • the defibration was carried out in a pressurized chip refiner, and the yield obtained was 93-94%.
  • the pulp was beaten in three steps at an edge load of 0.3 to 0.5 Ws/m and a net energy consumption of 100 kWh/ton corresponding to a gross energy consumption of 160 kWh/ton.
  • This embodiment is an example of how in the first step extruders can be used for coarse-disintegrating wood material. According to the example an extruder of the type Bivis was used.
  • Spruce chips were steamed in the usual manner at 100 o C for 10 minutes, whereafter they were fed into a Bivis-machine. At the defibration in the machine 2-3% sodium sulphite solution was charged so that the sulfonation degree of the material amounted to 1.5 g of sulphur per kg wood. The electric energy consumtion was about 400 kWh/ton wood when the material passed through the four compression zones of the twin-screw. After discharge, the fibre material was diluted to about 5% pulp concentration at about 70 o C, whereafter the suspension was pumped to beating in seven steps in a low concentration refiner.
  • the freeness of the pulp was about 250 ml CSF
  • the tensile index was 55 kNm/kg
  • the tear index 6 Nm2/kg at a net energy consumption of 150 kWh/ton and a gross energy consumption of 250 kWh/ton.
  • the total energy consumption for the manufacture of chemi-mechanical pulp (CTMP) to a freeness value of 250 ml CSF by the method according to the invention thus, amounts to 650 kWh/ton, which is to be compared with about 1750 kWh/ton according to the best conventional technique for obtaining the same freeness value.

Landscapes

  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Mechanical Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Paper (AREA)

Abstract

The invention relates to a method of manufacturing mechanical and chemi-mechanical papermaking pulp with low energy input by disintegrating and beating wood material in at least two steps. According to the invention, the material is coarse-disintegrated in a first step at a concentration exceeding 20 %, acid groups in the wood material are neutralized, the material is diluted to a concentration of 1-10 % and beaten in one or several steps.

Description

  • This invention relates to a method of making mechanical and chemi-mechanical papermaking pulp by disintegrating and beating wood material in at least two steps.
  • One object of the invention is to carry out the disintegration and beating in such a manner, that the total energy consumption is substantially reduced, as will be be described in the following.
  • The beating of cellulose-containing material at low pulp concentration is a method, which has been employed since long in order to improve the paperforming properties of the fibres. This applies, however, only to fibres free of lignin or substantially free of lignin, such as fibres produced according to the sulphate or sulphite method. As regards pulps manufactured mechanically, such as thermomechanical pulp (TMP) or chemi-mechanical pulp (CTMP), beating at low concentration, so-called post-refining, was not considered applicable other than as a method for increasing the light-scattering capacity of the pulps and for reducing slightly the fibre length and thereby improving the formation at the making of paper.
  • Investigations have been carried out previously to re-beat at lower concentrations a TMP manufactured at high concentration. In Scan Forsk Rapport 409/1984, for example, works are reported concerning energy consumption at re-beating at low concentration compared with refining at high concentration. The results from this investigation show that the freeness of TMP can be lowered by 10-30 ml without essentially deteriorating the strength properties, and that an energy saving of 50-150 kWh/ton could be achieved. The total energy consumption, however, was considerable and of the magnitude 1600 to 2300 kWh/ton.
  • In Pulp and Paper Magazine of Canada, Vol. 81, No 6, June 1980, page 72-80 (N.Hartler) experiments are reported to reduce the energy consumption at the refining of chips. One proposal made here is to change the chemical environment by the addition of chemicals. By adding sodium hydroxide the energy consumption could be reduced by 30%, but the total consumption yet amounts to about 1300 kWh/ton. At these experiments, however, the yield was deteriorated slightly and the ISO-brightness considerably.
  • In Svensk Papperstidning, 1982, page R 132-139 (P.Axelson and R.Simonson) the effect of sulphite impregnation of the chips on the refining process, a.o. the energy consumption, is discussed. At a certain amount of sulphite taken-up, the energy consumption diagram showed a minimum. Totally, however, the energy consumption was on a high level of 2000 kWh/ton.
  • Experiments have been carried out previously to treat thermomechanical pulp with fibre-modifying chemicals. It was then found, that by treating the defibered pulp with ozone prior to the refining in a two-step process the energy consumption could be lowered by up to 30%. This, however, could be achieved only at the expense of the yield.
  • In WO-A-87106280 the addition of alkali is disclosed.
  • According to the present invention it has proved possible to manufacture mechanical papermaking pulp by a substantially reduced energy consumption.
  • This is achieved according to the invention, in that the wood material in a first step is coarse-disintegrated at a concentration of above 20%. The energy input here shall be at maximum 8oo kWh/ton wood material. The acid groups included in the wood material thereafter shall be neutralized entirely or partially, and the material be diluted with water of a temperature corresponding to the softening temperature of the lignin. The dilution water shall have an ion strength of at maximum 0.05 mole per litre. The coarse-disintegrated material then shall be beaten at a concentration of 1-10% with an energy input of totally a maximum of 500 kWh/ton material.
  • The present invention is based on the idea that there is a relation between the disintegration of the wood material to fibres and the way, in which the energy pulses are transferred to the material, i.e. whether the energy pulses are transferred in liquid phase or steam phase. Attention also is to be paid to the thermal and physical state of the wood material when the energy pulses are being transferred.
  • One has not been successful previously by beating at low concentration to defibre the wood package in order to reduce the energy consumption at the manufacture of mechanical pulps. The reason is, that one did not know how to avoid the clipping of the fibres and thereby the much too low tensile and tear index of the resulting mechanical pulp and at the same time to bring about improved binding properties of the pulp.
  • In order to achieve this, it is important to accurately control the temperature and chemical environment of the fibre suspension in connection with the beating.
  • For obtaining a low total energy consumption, the energy input in the first coarse-defibering step must be low. The first high concentration step can be at atmospheric pressure or pressurized and be carried out by tearing (shredding), chip pressing, plug screwing (type Impressafiner or PREX) or by defibering in a refiner.
  • The final beating then takes place in one or several steps at low pulp concentration, i.e. at a concentration of 1-10%. At this beating must be observed, that the specific edge load is sufficiently low, and that the temperature and chemical environment of the fibre suspension has been adjusted to the softening and swelling state of the wood polymers. This implies according to the invention, that the temperature at the beating shall be at least as high as the softening temperature of the stiffest amorphous wood polymer, that the acid groups of the wood polymers substantially are ionized, and that the ion strength of the process water is sufficiently low.
  • The invention is described in the following in greater detail by way of some embodiments and with reference to to the accompanying drawings, in which
    • Fig. 1 is a flow sheet of an embodiment of the method according to the invention,
    • Figs. 2-4 are diagrams of properties and energy consumption of a pulp manufactured according to Fig. 1,
    • Fig. 5 is a flow sheet of a second embodiment of the invention, and
    • Figs. 6-8 show properties and energy consumption at the method according to said second embodiment.
    EXAMPLE 1
  • The flow sheet according to Fig. 1 illustrates the manufacture of thermomechanical pulp for newsprint.
  • Chips from spruce were steamed in a first step and preheated. The preheated chips then were disintegrated in a pressurized refiner with an energy consumption of 700 kWh/ton. At this coarse-defibering 3 kg NaOh were added in the beating zone of the refiner for neutralizing acid groups included in the wood material. To the defibered material dilution water with a temperature of 80oC and an ion strength of 2.0 mmole/l was added in order to obtain a pulp concentration of 3%.
  • At this concentration the pulp then was beaten in five subsequent steps at a specific edge load of 0.3-0.5 ws/m and a total net energy consumption of 150 kWh/ton pulp corresponding to a gross energy consumption of 250 kWh/ton pulp to a freeness of 150 ml CSF and a mean fibre length (PML) of 1.8 mm, i.e. about equal to TMP-pulp manufactured in conventional manner with an energy consumption of 1750 kWh/ton pulp.
  • The total energy consumption at the method according to the invention, thus, was reduced from 1750 to 950 kWh/ton pulp.
  • The yield amounted to about 97%.
  • A comparison between the properties for a TMP-pulp manufactured conventionally and one manufactured according to the invention appears from Table 1.
  • In this connection should be mentioned, that as conventional TMP-process the refining system was used, which up till now was known as the least energy requiring one, i.e. a pressurized twin-disc refiner combined with short dwell time at the pressurized preheating.
  • When two-step processes with single-disc refining are used, in most cases more than 2000 kWh/ton are required for obtaining a pulp with 150 m/CSF. TABLE 1
    T M P
    conventioan Invention
    Energy consumption,kWh/ton 1750 950
    Freeness, ml CSF 150 150
    PML x), mm 1.9 1.9
    Shives content,Sommerville % 1.3 0.5
    Tensile index, kNm/kg 32.0 32.0
    Tensile stiffness index 3.4 3.4
    Stretch at break, % 2.0 1.9
    Tear index, Nm²/kg 6.5 5.5
    Density, kg/m³ 380 380
    S, m²/kg 58.0 58.0
    ISO-brightness, % 60 60
    x) PML = mean particle length measured according to SIFI pulp measuring system
  • The manufacture of TMP according to the invention is compared in Fig. 2, 3 and 4 with TMP manufactured conventionally with single-step refining in twin-disc refiner, which is the least energy consuming TMP-process existing with the present state of art.
  • Fig. 2 shows the tensile index as a function of the electric energy consumption. It appears clearly from the Figure, that the increase in tensile index at a certain electric energy consumption is considerably greater for TMP manufactured according to the invention.
  • Fig. 3 shows the tear index as a function of the tensile index for TMP according to the invention and conventional TMP. It appears that the development of the tear index for the respective TMP is about the same, i.e. at optimation of the low concentration beating according to the invention the fibre cutting and thereby the serious decrease in tear index are substantially entirely avoided, which cutting and decrease occur usually at conventional low concentration beating of mechanical pulps.
  • Fig. 4 shows how the light-scattering coefficient (s) develops at conventional TMP and TMP manufactured according to the invention. It appears that the s-development requires as low an electric energy input as the tensile index development, i.e. the saving of electric energy to a certain s-value is of equal size as the saving of electric energy to a certain tensile index value.
  • EXAMPLE 2
  • This example relates to the manufacture of chemi-mechanical pulp (CTMP or CMP) according to the flow sheet shown in Fig. 5.
  • The treatment with impregnation chemicals, which can be sulphites, peroxide, oxygen gas, ozone and/or liquor, can take place prior to the first defibering step, after this step but prior to the final beating, after the final beating, or at combinations of these. In the flow sheet shown the impregnation is carried out prior to the first defibering step.
  • The first defibering step at high concentration is carried out in the same way as in Example 1.
  • At the manufacture of chemi-mechanical pulp the washing step is very essential, so that according to the invention the beating shall take place at low ion strength. The washing, therefore, is carried out prior to the final beating. In cases when the chemical treatment is carried out as the last process step, washing takes place even after this step.
  • The final beating takes place in the same way as according to Example 1, but process temperature and chemical environment must be adjusted to the special properties, which the wood polymers have assumed by treatment with impregnation chemicals. It is essential to pay regard to the number of sulphonic acid groups, which have been introduced by possible sulphite treatment. As an increasing amount of sulphonic acid groups reduces the softening temperature of the lignin, the temperature of the process water can be lower than at the manufacture of TMP-pulp according to Example 1. A sufficiently high temperature at the manufacture of CTMP is 40oC. From a brightness point of view it is advantageous to use the lowest possible temperature. By sodium sulphite treatment both the sulphonic acid groups and the carboxylic acid groups ate ionized from the beginning.
  • When at the manufacture of CTMP it is chosen to modify the wood with peroxide, oxygen or ozone, certainly no sulphonic acid groups are obtained, but the content of the wood material, especially of the lignin, of carboxylic acid groups increases considerably, which implies lowering of the softening temperature of the lignin.
  • In the eaxmple according to Fig. 5 chips from spruce were steamed and impregnated with a sodium sulphite solution in an amount corresponding to a 2% charge, whereafter they were preheated at a temperature of 130oC for 3 minutes. The material was then coarse-disintegrated with an energy consumption of about 600 kWh/ton in a pressurized chip refiner at high concentration (about 35%). The resulting yield amounted to about 96%. The coarse-defibered material obtained was diluted to about 3% and latency treated at 80oC for 20-30 minutes. The pulp was pressed to a concentration of 45-50% and again diluted to 3% at a temperature of 70oC. At this concentration the pulp then was beaten with a specific edge load of 0.3-0.5 Ws/m in five subsequent steps with a net energy consumption of 150 kWh/ton corresponding to a gross energy consumption of 250 kWh/ton for obtaining a pulp with a freeness of 250 ml CSF and a mean fibre length (PML) of 1.7 mm, i.e. as a conventionally manufactured CTMP-pulp produced in one step with an energy consumption of 1750 kWh/ton.
  • By the method according to the invention, thus, the energy consumption was reduced from the conventional 1750 kWh/ton to 850 kWh/ton.
  • The properties of the CTMP-pulp obtained compared with conventional CTMP-pulp are shown in Table 2. TABLE 2
    Conventional Invention
    Energy consumption,kWh/ton 1750 850
    CSF ml 250 250
    PML, mm - 1.7
    Tensile index, kNm/kg 40 40
    Tensile stiffness index - 4.6
    Stretch at break, % 1.9 1.6
    Tear index Nm²/kg 6.7 5.5
    Density, kg/m³ 420 450
    S, m²/kg 43 45
    ISO-brightness, % 60 60
  • The manufacture of CTMP according to the invention is compared in Figs. 6,7 and 8 with manufacture according to conventional technique.
  • In Fig. 6 the tensile index is shown as a function of the energy consumption for a CTMP-pulp manufactured according to the invention and for pulp manufactured conventionally. Compared at a certain tensile index, for example 40 kNm/kg, conventional refining consumes about 1750 kWh/ton pulp while at the method according to the invention only about 850 kWh/ton are consumed.
  • At a comparison of the method according to the invention with conventional method in a relationship with the tear index as a function of the tensile index, it appears that the relationships are similar, i.e. one avoids the fibre cutting, which is usual at low concentration beating and which gives rise to a substantially reduced tear index. This appears from the diagram in Fig. 7.
  • The light-scattering coefficient of the CTMP-pulp manufactured according to the invention as a function of the energy consumption is shown in the diagram in Fig. 8 compared with conventionally manufactured pulp. It shows here that according to the invention the energy consumption to a certain light-scattering index is substantially lower.
  • EXAMPLE 3
  • This example relates to the manufacture of highly sulfonated CTMP or CMP, i.e pulp containing more than 4 g of bound sulphur per kg wood material.
  • Chips from spruce were impregnated with a sodium sulphite solution containing about 120 g of sodium sulphite per litre in an amount corresponding to a charge of about 12%. The chips were preheated at a temperature of 140oC for 10 minutes, whereafter they were coarse-disintegrated with an energy consumption of about 400 kWh/ton wood. The defibration was carried out in a pressurized chip refiner, and the yield obtained was 93-94%. After a latency treatment at 60oC for 20-30 minutes at a pulp concentration of 3%, the pulp was beaten in three steps at an edge load of 0.3 to 0.5 Ws/m and a net energy consumption of 100 kWh/ton corresponding to a gross energy consumption of 160 kWh/ton.
  • The properties of the resulting pulp were determined, and in the following Table 3 the values obtained are stated in comparison with a CTMP manufactured in a conventional way in a one-step process with an energy input of 1500 kWh/ton. TABLE 3
    Conventional Invention
    Energy consumption, kWh/ton 1500 560
    CSF, ml 400 400
    PML, mm 1.9 1.9
    Tensile index, kNm/kg 65 65
    Stretch at break, % 2.0 1.8
    Tear index, Nm²/kg 8.0 8.0
    Density, kg/m³ 440 450
    S, m²/kg 34 36
    ISO-brightness, % 59 59
  • EXAMAPLE 4
  • This embodiment is an example of how in the first step extruders can be used for coarse-disintegrating wood material. According to the example an extruder of the type Bivis was used.
  • Spruce chips were steamed in the usual manner at 100oC for 10 minutes, whereafter they were fed into a Bivis-machine. At the defibration in the machine 2-3% sodium sulphite solution was charged so that the sulfonation degree of the material amounted to 1.5 g of sulphur per kg wood. The electric energy consumtion was about 400 kWh/ton wood when the material passed through the four compression zones of the twin-screw. After discharge, the fibre material was diluted to about 5% pulp concentration at about 70oC, whereafter the suspension was pumped to beating in seven steps in a low concentration refiner. After the fifth beating step, the freeness of the pulp was about 250 ml CSF, the tensile index was 55 kNm/kg, and the tear index 6 Nm²/kg at a net energy consumption of 150 kWh/ton and a gross energy consumption of 250 kWh/ton.
  • The total energy consumption for the manufacture of chemi-mechanical pulp (CTMP) to a freeness value of 250 ml CSF by the method according to the invention, thus, amounts to 650 kWh/ton, which is to be compared with about 1750 kWh/ton according to the best conventional technique for obtaining the same freeness value.
  • By beating in seven low concentration steps according to the invention, a freeness value of 50 ml CSF can be obtained, and the resulting CTMP-pulp is suitable for use in magazine and LWC-paper. The total energy consumption yet can be kept below about 850 kWh/ton. Pulp of this lastmentioned type cannot be manufactured with conventional technique,because then a sufficiently good smoothness cannot be achieved.
  • The invention is not restricted to the embodiments described, but can be varied within the scope of the invention idea.

Claims (4)

  1. A method of manufacturing mechanical and chemi-mechanical papermaking pulp with low energy input by disintegrating and beating wood material in at least two steps, characterized in that the material is coarse-disintegrated in the first step at a concentration above 20% with an energy input of at maximum 800 kWh/ton wood material, £hat acid groups existing in the wood polymers are neutralized entirely or partially by the addition of NaOH in an amount of at maximum 9 kg/ton, that the material is diluted by water with a temperature corresponding to the softening temperature of the lignin, i.e. 40-95oC, and with an ion strength of at maximum 0.05 mole per litre, and that the material then is beaten in one or several steps at a concentration of 1-10% with an energy input of totally at maximum 500 kWh/ton material.
  2. A method as defined in claim 1, characterized in that at least 25% of the total energy input is supplied at the beating.
  3. A method as defined in claim 1, characterized in that the coarse-disintegrated material after the first step is washed in order to reduce the ion strength.
  4. A method as defined in any one of the preceding claims, characterized in that the energy input in each beating step amounts to 50-150 kWh/ton pulp.
EP19890905472 1988-05-06 1989-04-05 Method of making mechanical and chemi-mechanical papermaking pulp Expired - Lifetime EP0413736B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT89905472T ATE94596T1 (en) 1988-05-06 1989-04-05 PROCESS FOR PRODUCTION OF MECHANICAL OR CHEMICAL-MECHANICAL PAPER PULP.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE8801731 1988-05-06
SE8801731A SE461103B (en) 1988-05-06 1988-05-06 PREPARATION OF MECHANICAL AND CHEMICAL MECHANICS IN TWO STEPS

Publications (2)

Publication Number Publication Date
EP0413736A1 EP0413736A1 (en) 1991-02-27
EP0413736B1 true EP0413736B1 (en) 1993-09-15

Family

ID=20372264

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19890905472 Expired - Lifetime EP0413736B1 (en) 1988-05-06 1989-04-05 Method of making mechanical and chemi-mechanical papermaking pulp

Country Status (7)

Country Link
EP (1) EP0413736B1 (en)
JP (1) JPH03504256A (en)
CA (1) CA1320067C (en)
DE (1) DE68909231T2 (en)
FI (1) FI91787C (en)
SE (1) SE461103B (en)
WO (1) WO1989010998A1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE9002039D0 (en) * 1990-06-07 1990-06-07 Svenska Traeforskningsinst SAVE TO PREPARE
US5853534A (en) * 1992-12-30 1998-12-29 Sunds Defibrator Industries Ab Method of producing pulp with high yield using a two-stage refining system operating at different temperatures
US6899791B2 (en) 1997-08-08 2005-05-31 Andritz Inc. Method of pretreating lignocellulose fiber-containing material in a pulp refining process
US8734611B2 (en) * 2008-03-12 2014-05-27 Andritz Inc. Medium consistency refining method of pulp and system
SE540961C2 (en) * 2016-05-23 2019-01-29 Holmen Ab Method of providing a paper fibre composition by combining chemical and mechanical pulping

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE409476B (en) * 1978-02-17 1979-08-20 Sca Development Ab KIT FOR REFINING LIGNOCELLULOSE-MATERIAL
JPS564791A (en) * 1979-06-18 1981-01-19 Kogyo Gijutsuin Bleaching of mechanical pulp
CA1246374A (en) * 1983-10-24 1988-12-13 Steve Rowland Two stage high consistency refiner
SE456826B (en) * 1986-04-18 1988-11-07 Svenska Traeforskningsinst SET TO REDUCE ENERGY CONSUMPTION BY REFINING CELLULOSALLY MATERIAL

Also Published As

Publication number Publication date
FI91787C (en) 1994-08-10
CA1320067C (en) 1993-07-13
SE8801731L (en) 1989-11-07
WO1989010998A1 (en) 1989-11-16
DE68909231D1 (en) 1993-10-21
JPH03504256A (en) 1991-09-19
SE461103B (en) 1990-01-08
FI91787B (en) 1994-04-29
EP0413736A1 (en) 1991-02-27
SE8801731D0 (en) 1988-05-06
DE68909231T2 (en) 1994-04-28
FI905482A0 (en) 1990-11-05

Similar Documents

Publication Publication Date Title
Lindstrom Chemical factors affecting the behaviour of fibres-during papermaking
US4798651A (en) Process for preparing pulp for paper making
JP2915576B2 (en) CTMP process
EP2625330B1 (en) Method for producing a high-freeness pulp
US4756799A (en) Method of manufacturing bleached chemimechanical and semichemical fibre pulp by means of a one-stage impregnation process
US4486267A (en) Chemithermomechanical pulping process employing separate alkali and sulfite treatments
US4869783A (en) High-yield chemical pulping
EP1552052B1 (en) A method of producing mechanical pulp and the mechanical pulp thus produced
US5338405A (en) Production of fiber pulp by impregnating the lignocellulosic material with an aqueous alcoholic SO2 solution prior to defibration
US4900399A (en) Method of manufacturing bleached chemi-mechanical and semichemical fibre pulp by a two-stage impregnation process
US9139955B2 (en) Method of processing chemical pulp
EP0501059A1 (en) Steam explosion pulping process for papermaking
US5007985A (en) Method of reducing the energy consumption at the refining of cellulose containing material
US2169473A (en) Method of producing cellulose pulp
EP0413736B1 (en) Method of making mechanical and chemi-mechanical papermaking pulp
US3829357A (en) Oxidative manufacture of pulp with chlorine dioxide
WO2004050983A1 (en) Method and system for treatment of wood chips
US3192102A (en) Pulping process
US3013931A (en) Printing paper and process of making the same
EP0030778B1 (en) Process for the formation of refiner pulp
Howard The effects of recycling on pulp quality
AU671159B2 (en) Improved bleaching of high consistency lignocellulosic pulp
JP2003027385A (en) Method for producing mechanical pulp
Petit-Conil¹ et al. High-yield pulps: an interesting concept for producing lignocellulosic fibers
US4836892A (en) Pulp blends for linerboards

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19901008

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH DE FR GB IT LI LU NL SE

17Q First examination report despatched

Effective date: 19921127

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE CH DE FR GB IT LI LU NL SE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Effective date: 19930915

Ref country code: LI

Effective date: 19930915

Ref country code: NL

Effective date: 19930915

Ref country code: BE

Effective date: 19930915

Ref country code: CH

Effective date: 19930915

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRE;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.SCRIBED TIME-LIMIT

Effective date: 19930915

REF Corresponds to:

Ref document number: 94596

Country of ref document: AT

Date of ref document: 19931015

Kind code of ref document: T

REF Corresponds to:

Ref document number: 68909231

Country of ref document: DE

Date of ref document: 19931021

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

ET Fr: translation filed
NLV1 Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Effective date: 19940405

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19940430

REG Reference to a national code

Ref country code: FR

Ref legal event code: TP

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 19940405

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 19970326

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 19970328

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: AT

Payment date: 19970421

Year of fee payment: 9

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19980405

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: THE PATENT HAS BEEN ANNULLED BY A DECISION OF A NATIONAL AUTHORITY

Effective date: 19980430

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19990202

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST