WO1997022749A1 - Process for treating refiner pulp - Google Patents

Process for treating refiner pulp Download PDF

Info

Publication number
WO1997022749A1
WO1997022749A1 PCT/IB1995/001140 IB9501140W WO9722749A1 WO 1997022749 A1 WO1997022749 A1 WO 1997022749A1 IB 9501140 W IB9501140 W IB 9501140W WO 9722749 A1 WO9722749 A1 WO 9722749A1
Authority
WO
WIPO (PCT)
Prior art keywords
pulp
pulps
chemical
adjust
treated
Prior art date
Application number
PCT/IB1995/001140
Other languages
French (fr)
Inventor
Michel C. Barbe
Sophie Janknecht
Lyne Proulx
Jean St-Yves
Original Assignee
Kvaerner Hymac Inc.
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 Kvaerner Hymac Inc. filed Critical Kvaerner Hymac Inc.
Priority to AU42715/96A priority Critical patent/AU4271596A/en
Priority to PCT/IB1995/001140 priority patent/WO1997022749A1/en
Publication of WO1997022749A1 publication Critical patent/WO1997022749A1/en

Links

Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21CPRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C9/00After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
    • D21C9/001Modification of pulp properties
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21BFIBROUS RAW MATERIALS OR THEIR MECHANICAL TREATMENT
    • D21B1/00Fibrous raw materials or their mechanical treatment
    • D21B1/02Pretreatment of the raw materials by chemical or physical means
    • D21B1/021Pretreatment of the raw materials by chemical or physical means by chemical means
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21CPRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C3/00Pulping cellulose-containing materials
    • D21C3/22Other features of pulping processes
    • D21C3/26Multistage processes

Abstract

Process for producing lignocellulosic pulp fibers with improved properties by treating the refiner pulp with chemicals to adjust the pH, treating it at high temperature and with chemical charges, and thereafter subject it to a refining step.

Description

PROCESS FOR TREATING REFINER PULP
FIELD CF THE INVENTION
The present invention relates to a process for producing lignocellulosic pulp in accordance with the preamble to the attached Claim 1.
BACKGROUND OF THE INVENTION
The pulp and paper industry uses many processes to produce pulp from lignocellulosic materials such as softwoods, hardwoods or annual plants. These are used for the manufacture of several paper grades such as newsprint, speciality papers (LWC, SC, ... ) and fine papers (Art, MFC, ... ).
Chemical pulps used in fine papers are prepared by cooking the wood chips at elevated temperatures and pressures with various chemical agents such as Na2S and NaOH at high pH (Kraft
pulping) and Na2SO3/NaHSO3 for sulfite/bisulfite pulping at neutral pH. In these processes, the purpose of the chemical agents is to degrade and dissolve the lignin and the
hemicellulose material in wood to leave pure cellulose fibers in the 40-45% yield level. Following this process, chemical fibers are bleached to high levels such as 85-90% ISO-brightness. The fibers are flexible and high strength papers can be produced from them. Chemical pulps are therefore also used in producing newsprint and speciality papers to provide dry strength to the sheet to ensure good runability in the press room. There are several problems associated with chemical pulping, however, with decreasing forest resources for
instance, the resulting low yield from the process implies that a substantial amount of trees must be harvested. Furthermore, chemical pulping processes require high levels of fresh water and toxic chlorinated by-products (dioxin and AOX) are found in the effluent. Odour emissions are also noteworthy. Sulfur emissions contribute to acid rain, which is responsible for forest deterioration and depletion of the soil.
Mechanical pulps of inferior strengtn are also used in the manufacture of newsprint and speciality papers because of their high light scattering coefficient or opacity as well as high oil absorbancy which is required for ink acceptance during printing. In the production of these pulps, mechanical means are used For instance, grindstones are used to defiber logs in the stone groundwood process (SG). Disc refiners are also used to defiber wood chips into pulp. Wood chips can be refined without any specific treatment such as in refiner mechanical pulping (RMP). The wood chips can also be thermally treated at temperatures oetween 100 to 130°C prior to being refined such as in the thermomechanical process (TMP). In these processes, approximately five percent of the wood substance that is water soluble is lost for a net yield of approximately 95%. The strength of the resulting pulps is directly related to the degree of mechanical energy applied to the fibers in the form of shear stresses in the refining zone. The energy transferred to fibers is used to increase their flexibility. The internal cell wall dislocation or fibrillation resulting from bending and torsional stresses imposed onto fibers in the refining zone enhances their flexibility, bat often this increased
flexibility is obtained with reduction in fiber length. It is generally recognized that there are three problems in the manufacture of refiner mechanical pulp. One is the reduced strength of the paper formed from the pulp because the fibers are chopped and abraded. The second is the high electrical demand of the refiner or high specific refining energy The third is the low brightness of the pulp produced.
Mechanical pulps lack the desirable strength properties to replace, in whole or in part, low-yield chemical pulps, e.g kraft or sulphite pulps, in linerboard, newsprint, tissue, printing grades and coated-base grade of paper Consequently, it has been an aim of the art to improve the physical and optical properties of mechanical pulps, so that such improved pulps would be used to replace low-yield chemical pulps. The major problem has been the significant quantity of electrical energy to comminute the wood chips into a useable pulp.
Impregnating wood chips with chemicals such as sulfite has been used to improve the strength and optical properties of refiner mechanical pulps. For instance, U.S. Patent 3,446,699 issued May 27, 1965 to Asplund et al. provides a method for producing mechanical and chemimechanical or semi-chemical pulps from lignoceilulose-containing material, in order to provide
improved quality of the fibers with improved defloration.
U.S. Patent 3,558,428 issued Jan. 25, 1971 to Asplund et al. provided a method for manufacturing chemimechanical pulps involving heating and defibrating the same in an atmosphere of vapour at elevated temperature and under corresponding pressure of the impregnated chips to provide a more rapid and effective impregnation. In this chemi-thermomechanical pulping processes (CTMP) in which the yield range is between 88-92%, the wood chips are treated with relatively small amounts of sulfite and bisulfite which modifies the lignin by sulfonating it
sufficiently to produce a marked change in its physical and chemical properties which give rise to brightness and strength improvement. However, the lignin is not made completely soluble in water or in the cooking liquor so that relatively high yields are obtained. Chemical impregnation of chips also results in lower debris but usually increases the long fiber content and reduces the scattering coefficient. Increases in energy requirement of 15-25% are observed to reach a given drainage or CSF level.
Falling midway between the chemical and mechanical processes are the semi-chemical and chemi-mechanical pulping processes (CMP). The yield range of the resulting pulps is between 60-85% so that good pulp properties are achieved at low refining energy by cooking the wood chips (or other cellulosic material) under severe conditions. Typical temperatures are in the 16024C°C range with high chemical charges to degrade a great deal of the lignin and hemicellulose. Cooking times range between one to four hours. As an example, U. S. Patent 4,115,758 issued Sept. 26, 1978 to M.J. Ford provided a process for producing high-yield chemimechanical pulps from woody lignoceiiulose material by treatment with an aqueous solution of a mixture of sulfite and bisulfite, to provide a pulp which can be readily defibered by customary mechanical means. The resulting pulp has different characteristics depending on the yield and refining energy applied as demonstrated by M. Barbe et al., Journal of Pulp and Paper Science, 12(5): J141-146 (September 1986).
An alternate approach to improve the quality of mechanical pulps has been to treat the refiner pulp fibers. Two processes are currently used commercially. In the first process,
described by A. Barnet et al. , Pulp and Paper Canada 81, T255-T260 (1980), TMP pulp fibers are being treated at 160°C for 45- 60 minutes in a reactor with sodium sulfite charges of 12-14% at pH of 9.8. The yield obtained is in the range of 65 - 88 % . The ref ining energy to a given freeness is reduced while the
strength properties are improved. The high chemical charges, low yield and therefore high effluent loads combined with the high cost for a reactor of appreciable size, as well as the dewatering or washing equipment required, offsets the benefits achieved. Therefore, this process alternative has not received wide commercial acceptance in the industry. In the second process, described by M. Barbe et al., World Pulp and Paper Technology 1991, Frank Roberts, editor, Sterling Publications International Limited, London (1991), CTMP pulp fibers are being treated at medium consistency (12%) and at 60°C for 120 minutes with an alkaline peroxide liquor at pH of 10-11.
The yield obtained with this process is in the range of 80-85%. Savings in refining energy to reach a given freeness are obtained. The drawbacks of this latter process are similar to those of the first process alternative. The low yield, high effluent loads and chemical charges combined with the high costs for bleaching towers with two hours retention time, with their discharge mechanisms as well as the cost for the
dewatering or washing equipment required, offsets the benefits achieved. Therefore, this process alternative has not received wide commercial acceptance in the industry.
The low brightness of mechanical pulps is clearly a major problem which has limited their use in different paper grades Several processes are currently employed in the pulp and paper industry to bleach mechanical or chemithermomechanical pulps. One process uses a reducing agent such as dithionite or sodium and zinc hydrosulfite (Y) to brighten or bleach the pulps. With this bleaching chemical moderate gains of 4 to 10 points are obtained. Maximum brightness levels of 68 to 70% ISO can be reached with the addition of approximately 1% to 1.25% on o.d. pulp of sodium hydrosulfite. The process is usually carried out in an aqueous phase at 3 to 5% consistency, a pH of 4.5 to 6.0, a temperature of about 60°C and a retention time of up to one hour. The use of a chelating or sequestering agent such as sodium tripolyphosphate (STPP) to remove naturally occurring trace metals is recommended. Peroxide (P) is also employed for bleaching. The process is carried cut in a single tower or in two bleaching towers. In both cases, the bleaching is done at a pulp consistency of 15 to 35%, moderate temperatures of 50 to 70°C, and retention times of two to three hours for each stage. Stabilizers such as sodium silicate and magnesium sulfate are added to the bleach liquor to prevent peroxide decomposition. Sodium hydroxide is also used to maintain an alkaline pH of 9.5 to 11 so as to increase the concentration of the perhydroxyl ion OOH which is believed to be the active bleaching agent.
Furthermore, pulps are normally pretreated at low consistency with organic chelating agents such as sodium diethylenetriamine penta-acetate (DTPA) to remove trace metals. All of the above bleaching processes involve the addition of high chemical charges and high costs in order to achieve the desired brightness levels. However, these permit to extend the use of the mechanical or chemimechanical pulps in a wide range of paper products. High capital costs in equipment are
required.
It is well known that the physical properties of wood pulps are strongly influenced by the flexibility of the individual fibers. In the papermaking process, the fibers are brought into close contact with each other by surface tension forces in the water removal process or during the pressing stages of the process Flexible fibers therefore lead to better bonding and improved strength. Natural wood fibers are inflexible due to the presence of large amounts (20-30% by weight) of lignin and crystalline cellulose (30-40% by weight). All of the prior art indicate that fiber flexibility has been improved in
conventional mechanical pulping by applying mechanical energy to the fibers and in chemical or semichemical or chemi-mechanical pulping processes by removing part, or nearly all, of the lignin or in some other cases by modifying its chemical nature with sulfonation in addition to the mechanical energy. However, in mechanical pulping the increased fiber flexioility and sheet strength is limited as the increase in flexibility is done with cell wall dislocations that reduce fiber strength and fiber length. In chemimechanical pulping, or with the existing pulp fiber treatment process, the increased fiber flexibility and sheet strength is obtained by reducing the yield of the pulp.
It is therefore an object of the present invention to provide a process which permits the treatment of lignocellulosic
materials so as to render the fibers flexible and conformable with low refining energy while improving the strength and brightness of the resulting pulp in addition to maintaining the materials yield for the production of pulp from weed chips and other lignocellulosic materials. In addition to the savings obtained with low refining energy, saving can also be obtained in capital cost requirements and in bleaching chemicals when the treated pulps are bleached to high levels with the current state of the art bleaching technology. Conversely, high brightness levels can be reached at a given bleaching chemical charge, therefore permitting to improve the quality of mechanical pulps to extend their use in the production of high quality paper grades in replacement of chemical fibers.
This object is obtained by the following process of the type described in the preamble to Claim 1 which is characterized by the following steps: a) mixing the lignocellulosic material with a puffer or chemical solution in a high shear mixer-reactor so as to adjust the pH of the pulp, while maintaining the pulp at high consistency, b) submitting the pulp to high temperature for times and chemical charges sufficient to reduce the long range crystalline structure of the cellulose component of wood, and c) subsequent by subjecting the lignocellulosic pulp fibers to refining to produce a pulp with the desired end- product properties.
The present invention will be explained in more detail with reference to the drawings of which:
Fig. 1 shows the energy reductions obtained when pulps are treated in accordance with the present invention as a function of the final pH of the pulp, Fig 2 shows the energy reductions obtained as a function of the total ionic content or yield,
Fig 3 shows the energy reduction/increase to be expected upon changes or variation in the sulfonate content of the fibers obtained with the present state of the art CTMP or CMP
technology,
Figs 4 and 5 are process flow diagrams illustrating the various steps of a continuous operation in which pulps are treated according to the present invention.
While the invention is not limited to any theory, it is believed that the process provides the savings in refining energy and improved properties by reducing the long range crystallinity of cellulose and by the chemical degradation of the lignin, hemicellulose and cellulose components of wood. Figure 1, showing energy reductions obtained following the treatment of the pulps according to the present invention, as a function of the final pH of the pulp, as well as Figure 2 showing energy reductions obtained as a function of the total ionic content or yield, indicate that savings can be obtained at low ionic content or high yield with treatments at low pH as well as at high total ionic content and high pH. Under low pH and ionic content conditions, it is believed that changes in the long range crystallinity of the crystalline structure of the cellulose prevails to give the savings in refining energy. The chemicals or buffers used inhibit the acid hydrolysis of the polysaccharides and therefore preserves fiber strength. At high pH or high ionic content, the chemical degradation of the lignin, hemicellulose and cellulose may prevail in addition to the changes in the crystalline structure of cellulose. Figure 3 shows the energy reduction/increase to be expected upon changes or variations in the sulfonate content of the fibers obtained with the present state of the art CTMP or CMP technology Figure 4 describes an application of the process by which a refined pulp obtained directly at the outlet of a refiner (1) is blown in a high shear mixer (2) in which a buffer or a chemical solution is added to adjust the pH of the pulp. The conditions for the treatment temperature or pressure as well as the desired retention time and chemical charge in the high shear mixer (2) are to be selected according to the initial pulp pH, wood species and desired benefits in either strength, optical or refining energy reduction to be sought.
Subsequently, the treated pulp is mechanically defiberized in a second refiner (3) which blows the pulp to a pressurized or atmospheric cyclone (4).
Figure 5 describes an application of the process by which a refiner pulp obtained at the discharge of a dewatering device such as a screw press (5), is fed with a pulp plug screw (6) into the high shear mixer (7). Buffers or a chemical solution is added to adjust the pH of the pulp while the treatment temperature or pressure as well as the desired retention time and chemical charge is set to achieve the desired benefits.
Subsequently, the treated pulp is mechanically defibered in a refiner (8) and blown into a pressurized or atmospheric cyclone (9).
THE FOLLOWING EXAMPLES ARE GIVEN TO ILLUSTRATE MORE CLEARLY VARIOUS EMBODIMENTS OF THE INVENTION.
Example 1
In this example, as well as in subsequent examples, the
following experimental procedure was used for the treatment of pulps. The different chemical agents were mixed with a refined pulp in a commercial high shear mixer, treated in a digester and subsequently refined on a 30 cm single disc refiner. The control pulps coded CB3N were only thermally treated in the digester prior to refining. The control pulps coded C-6N were simply refined in the single disc refiner without thermal treatment.
This example is intended to illustrate that when pulp fibers are treated in the presence of acids or bases to adjust the pH, as described for aspects of this invention, refining energy is reduced appreciably while the strength properties are improved.
Table 1 gives the quality of pulps treated compared to the treated pulp without buffers or chemicals (coded C3-3N) and the untreated pulp (coded C-6N).
The pulps coded C-6N give the properties of a pulp as produced by the current state of the art. The pulp coded CB-3N gives the properties of a pulp submitted to a thermal treatment without the addition of a buffer. The pulps coded A1-4N, A2-4N and 3-4N give the properties of a pulp submitted to a thermal treatment with the addition of NaOH or H2SO4, to adjust the pH as per the precept of this invention. It can be observed that reduction of refining energy of 25 to 64% are obtained compared to the untreated pulp. Higher energy reductions are obtained at high and low pH adjustment. It is preferable to treat the pulp at high pH levels to obtain high strength properties such as tensile index and breaking length. However, the tear index remains low. The pH adjustment allows the optimization of different pulp quality under conditions in order to obtain high yield pulps. Table 2 shows the effect of conventional peroxide bleaching on the pulp and paper properties for the pulps
treated with H2SO4 and the pulp treated without buffers or chemicals. The pulps treated at low pH show higher brightness level compared to the pulp treated without buffers or chemicals at a given chemical charge and higher brightness level is also reached following a peroxide bleaching stage. Therefore, reductions in peroxide consumption are expected to be reached at a given brightness level when the pulps are treated at low pH with buffers, compared to pulps treated without buffers or chemicals.
Example 2
This example illustrates the effect of pH of treatment upon adjustment with CO2 and calcium hydroxide (Ca(OH)2) .
Table 3 gives the quality of pulps treated compared to the treated pulp without buffers or chemicals (coded C3-3N) and the untreated pulp (coded C-6N).
The pulps coded C-6N give the properties of a pulp produced by the current state of the art. The pulp coded C3-3N gives the properties of a pulp submitted to a thermal treatment without the addition of a buffer. The pulps coded H2-5N and H3-6N give the properties of a pulp submitted to a thermal treatment with the addition of CO2 and CO2/Ca(OH)2, to adjust the pH as per the precept of this invention. It can be observed that refining energy reductions of 13 to 28% are obtained compared to the untreated pulps while maintaining a high yield. The strength properties of the treated pulps are lower compared to the untreated pulps. However, with the heat treatment, reductions in energy consumption are obtained with the use of CO2 or
CO2/Ca(OH)2 together with improved strength properties and brightness of the pulps. In addition to the above benefits, the combined use of the CO2 or CO2/Ca(OH)2 give rise to the
formation of CaCO3 which is used as a filter in the pulp and paper industry to confer high opacity to paper.
Example 3
This example illustrates the effect of sodium sulfite (Na2SO3) liquor used to control the pH of the heat treatment. In this example, pulps were heat treated with H2SO4 and NaOH in
combination with the Na2SO3 to control the pH. Table 4 gives the quality of pulps treated compared to the treated pulp without buffers or chemicals (coded C3-3N) and the untreated pulp (coded C-6N) .
The pulps coded C-6N give the properties of a pulp produced by the current state of the art. The pulp coded C3-3N gives the properties of a pulp submitted to a thermal treatment without the addition of a buffer. The pulps coded D1-3N, D2-7N, and D3- 7N give the properties of a pulp submitted to a thermal
treatment with the addition of Na2SO3 and H2SO4 or NaOH, to adjust the pH as per the precept of this invention.
It can be observed that refining energy reductions of 30 to 45% are obtained compared to the untreated pulps. The maximum energy reductions are obtained at low and high pH. It is preferable to treat the pulp at high pH to reach high strength properties such as tensile index or breaking length. However, the tear index is lower compared to untreated pulps. The pH adjustment allows the optimization of different pulp quality under different conditions while the high yield of the pulps is maintained. Table 5 shows the effect of conventional peroxide bleaching en the pulp and paper properties for the pulps treated with Na2SO2 at low pH and the pulp treated without buffers or chemicals. The pulps treated at low pH show higher brightness level compared to the pulp treated without buffers or chemicals. Higher brightness level is also reached following a peroxide bleaching stage. Therefore, reductions in peroxide consumption are also to be expected to reach a given brightness level when the pulps are treated with Na2SO3 at low pH compared to pulp treated without buffers or chemicals.
Example 4
This example illustrates the effect of reducing agents such as sodium hydrosulfite (Na2S2O4), sodium borohydride (NaBH4) and formamidine sulfinic acid (FAS) to control the pH of the pulp during heat treatment.
Table 6 gives the quality of pulps treated compared to the treated pulp without buffers or chemicals (coded C3-3N) and the untreated pulp (coded C-6N).
The pulps coded C-6N give the properties of a pulp produced by the current state of the art. The pulp coded CB-3N gives the properties of a pulp submitted to a thermal treatment without the addition of a buffer. The pulps coded C-1-5N, G2-4N, G3-5N, and H1-5N give the properties of a pulp submitted to a thermal treatment with the addition of Na2S2O4 and NaBH4 or FAS, to adjust the pH as per the precept of this invention.
It can be observed that refining energy reductions of 30 to 35% are obtained compared to the untreated pulps while maintaining a high yield. The strength properties of the treated pulps are lower compared to the untreated pulps. However, as a heat treatment reduces the energy consumption, it is shown that the addition of reducing agents may also improve the strength properties of the pulps. Under acidic conditions, the
brightness of the pulps is also improved compared to treated pulps without puffers or chemicals. Table 7 snows the effect of conventional peroxide bleaching en the pulp and paper
properties for the pulps treated with NaBH4 at high pH and the pulp treated without buffers or chemicals. The pulps treated at high pH show similar brigntness level compared to the pulp treated without buffers or chemicals. However, higher
brightness levels (approximately 10 points) are reached
following a peroxide bleaching stage. The pulps treated with a reducing agent have a better brightness response to peroxide bleaching compared to pulp treated with heat only. Therefore, reductions in peroxide are also expected to reach a given brightness level when the pulps are treated with a reducing agent at high pH compared to pulps treated without buffers or chemicals.
Example 5
This example illustrates the effect of oxidizing agents such as peroxide (H2O2), oxygen (O2) and a mixture of peroxide and oxygen. In this example, the pH of the pulps were adjusted with NaOH used with the H2O2 solution.
Table 8 gives the quality of pulps treated compared to the treated pulp without buffers or chemicals (coded CB-3N; and the untreated pulp (coded C-6N).
The pulps coded C-6N give the properties of a pulp produced by the current state of the art. The pulp coded C3-3N gives the properties of a pulp submitted to a thermal treatment without the addition of a puffer. The pulps coded D1-5N, F2-4N, and F3-4N give the properties of a pulp submitted to a thermal treatment with the addition of oxidizing agent and NaOH.
It can be observed that refining energy reductions of 11 to 27% are obtained compared to the untreated pulps The maximum energy reductions are obtained at high pH. It is preferable to treat the pulp at high pH levels to obtain high strength properties such as tensile index and breaking length. The pH adjustment allows the optimization of different pulp quality under conditions while high yield pulps are produced. In order to reduce the refining energy and to improve the strength properties as well as the brightness of the pulps, it is preferable to combine the thermal treatment with the addition of oxidizing agents. However, the tear index remains lower.
Table 9 shows the effect of conventional peroxide bleaching on the pulp and paper properties for the pulps treated with
oxidizing agents and the pulp treated without buffers or
chemicals. The pulps treated with oxidizing agents show higher brightness level compared to the pulp treated without puffers or chemicals. Higher brightness levels are also reached following a peroxide bleaching stage. Therefore, reductions in peroxide are also expected at a given brightness level when the pulps are treated with a reducing agent compared to the pulps treated without buffers or chemicals.
Example 5
This example illustrates the effect of oxidizing agents such as peracids made from a mixture of peroxymonosulfuric acid or Caro's acid (H2SO5) and peracetic acid (CH3CO3H). In this example, pulps were treated with adjustment of the pH with NaOH in combination with the mixture of H2SO5:CH3CO3H.
Table 10 gives the quality of pulps treated compared to the treated pulp without buffers or chemicals (coded C3-3N) and the untreated pulp (coded C-6N) .
The pulps coded C-6N give the properties of a pulp produced by the current state of the art. The pulp coded C3-3N gives the properties of a pulp submitted to a thermal treatment without the addition of a buffer. The pulps coded I1-4N, I2-3N, and I3-4N give the properties of a pulp submitted to a thermal treatment with the addition of oxidizing such as a mixture of H2SO5, NaOH, and NaOH to adjust the pH as per the precept of this invention.
It can be observed that refining energy reductions of
approximately 20% are obtained compared to the untreated pulps. To obtain full benefits in energy reduction, in addition to strength and optical properties, it is preferable to combine the heat treatment with the addition of oxidizing agents such as a mixture of Caro's acid and peracetic acid under acidic conditions. Table 11 shows the effect of conventional peroxide bleaching en the pulp and paper properties for the pulps treated with oxidizing agents and the pulp treated without buffers or chemicals. The pulps treated show lower brightness level compared to the pulp treated without buffers or chemicals but higher brightness level is reached following a peroxide bleaching stage. Therefore, reductions in peroxide are also expected at a given brightness level when the pulps are treated with peracid agents compared to the pulps treated without buffers and chemicals. The pH adjustment allows the
optimization of different pulp quality under selected
conditions while retaining their yield pulps.
Figure imgf000019_0001
Figure imgf000020_0001
Figure imgf000021_0001
Figure imgf000022_0001
Figure imgf000023_0001
Figure imgf000024_0001
Figure imgf000025_0001
Figure imgf000026_0001
Figure imgf000027_0001
Figure imgf000028_0001

Claims

1. A process by which lignocellulosic pulp fibers are produced at low specific refining energy and high yield, characterized by the following steps: (i) mixing the lignocellulosic pulp fibers with a buffer or chemicals to adjust the pH of the pulp while maintaining the pulp at high consistency,
(ii) submitting the pulp to high temperature for times and chemical charges sufficient to reduce the long range crystalline structure of the cellulose component of wood, and
(iii) subsequently subjecting the lignocellulosic pulp fibers to refining to produce a pulp with the desired end- produce properties.
2. A process of claims 1, characterized in that said pulp fibers are lignocellulosic pulp fibers obtained after impregnation of wood chips in a single or multistage impregnation with water, sulfite, bisulfite, peroxide solution, sodium borohydriae and sodium borohydride-caustic-sulfite liquor followed by refining.
3. The process of claim 1, characterized in that said
lignocellulosic material is a washed pulp or pretreated pulp with metal complexing agents to remove metal ions prior to the treatment.
4. The process of claim 1, characterized in that said
lignocellulosic pulp fibers are whole pulps from main line refining lines or are long fibers or rejects obtained from screening and cleaning stages.
5. The process of one of the preceding claims, characterized in that the chemical or buffer used to adjust the pH is an acid such as HCℓ, H2SO4 and H2CO3.
6. The process of one of claims 1-4, characterized in that the chemical or buffer used to adjust the pH is a base such as NaOH, Ca(OH)2 and Na2CO3.
7. The process of one of claims 1-4, characterized in that the buffer or chemical used is a mixture of Ca(OH2) and CO2 (g) or H2CO3.
8 The process of one of the preceding claims, characterized in that the chemicals used are oxidizing agents to adjust the pH below 7 which is, for instance, a mixture of oxygen (O2) and peroxide (H2O2), a mixture of ozone (O3) and peroxide (H2O2) and peracids (H2SO4-H2O2, CH3COOH-H2O2).
9. The process of one of the preceding claims, characterized in that the chemical used to adjust the pH above 7 is an oxidizing agent which is, for instance, peroxide (H2O2).
10. The process of one of the preceding claims, characterized in that the chemical used to adjust the pH above 7 is a
reducing agent such as sodium sulfite (Na2SO3), sodium
borohydride (NaBH4) and formamidine sulfuric acid (FAS).
11. The process of one of the preceding claims, characterized in that the chemical used to adjust the pH below 7 is, for instance, a reducing agent such as bisulfite (MHSO3) or acid sulfite (H2SO3 - MHSO3) (where M = Base = 1/2Ca+2, 1/2 mg+2, Na+, NH4 +) and dithonite or sodium hydrosulfite (Na2S2O4).
12. The process of one of the preceding claims, characterized by the subsequent steps of screening, cleaning, dewatering and brightening or bleaching sequences to upgrade further the brightness of the pulps.
PCT/IB1995/001140 1995-12-19 1995-12-19 Process for treating refiner pulp WO1997022749A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
AU42715/96A AU4271596A (en) 1995-12-19 1995-12-19 Process for treating refiner pulp
PCT/IB1995/001140 WO1997022749A1 (en) 1995-12-19 1995-12-19 Process for treating refiner pulp

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/IB1995/001140 WO1997022749A1 (en) 1995-12-19 1995-12-19 Process for treating refiner pulp

Publications (1)

Publication Number Publication Date
WO1997022749A1 true WO1997022749A1 (en) 1997-06-26

Family

ID=11004392

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB1995/001140 WO1997022749A1 (en) 1995-12-19 1995-12-19 Process for treating refiner pulp

Country Status (2)

Country Link
AU (1) AU4271596A (en)
WO (1) WO1997022749A1 (en)

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0824160A1 (en) * 1996-08-14 1998-02-18 Giesecke & Devrient GmbH Process for the manufacture of paper making pulp
WO1999054544A1 (en) * 1998-04-17 1999-10-28 Alberta Research Council Inc. Method of producing lignocellulosic pulp from non-woody species
WO2000077301A1 (en) * 1999-06-15 2000-12-21 Kemira Chemicals Oy Method to improve the opacity of mechanical pulp by using aliphatic peroxyacids and use of peroxyacids to improve opacity
WO2005045129A1 (en) * 2003-10-15 2005-05-19 Voith Paper Patent Gmbh Method for adjusting the ph and machine for preparing a fiber web
WO2007064287A1 (en) * 2005-12-02 2007-06-07 Akzo Nobel N.V. Process of producing high-yield pulp
WO2008132228A1 (en) * 2007-04-30 2008-11-06 Linde Aktiengesellschaft A method for reducing the energy consumption at the refining of a pulp suspension in a papermaking process and use of sodium bicarbonate in papermaking
WO2008135631A1 (en) * 2007-05-04 2008-11-13 Kemira Oyj Method for preparing dithionite
WO2009003770A1 (en) * 2007-07-03 2009-01-08 Linde Aktiengesellschaft Process for making paper and use of an acid/base treatment in papermaking
WO2010104725A1 (en) 2009-03-09 2010-09-16 Nalco Company Method and chemical composition to improve efficiency of mechanical pulp
EP2443280A1 (en) * 2009-06-15 2012-04-25 Arkema, Inc. Alkaline peroxide treatment of rejects in an integrated neutral-alkaline paper mill
US8262850B2 (en) * 2003-09-23 2012-09-11 International Paper Company Chemical activation and refining of southern pine kraft fibers
US8268122B2 (en) 2005-12-02 2012-09-18 Akzo Nobel N.V. Process of producing high-yield pulp
US20140124150A1 (en) * 2012-11-02 2014-05-08 Andritz Inc. Method for production of micro fibrillated cellulose
EP2924166A1 (en) * 2014-03-25 2015-09-30 Basf Se Method for the manufacture of bleached wood fibre
US9511167B2 (en) 2009-05-28 2016-12-06 Gp Cellulose Gmbh Modified cellulose from chemical kraft fiber and methods of making and using the same
US9512561B2 (en) 2009-05-28 2016-12-06 Gp Cellulose Gmbh Modified cellulose from chemical kraft fiber and methods of making and using the same
US9512237B2 (en) 2009-05-28 2016-12-06 Gp Cellulose Gmbh Method for inhibiting the growth of microbes with a modified cellulose fiber
US9512563B2 (en) 2009-05-28 2016-12-06 Gp Cellulose Gmbh Surface treated modified cellulose from chemical kraft fiber and methods of making and using same
US9932709B2 (en) 2013-03-15 2018-04-03 Ecolab Usa Inc. Processes and compositions for brightness improvement in paper production
US9951470B2 (en) 2013-03-15 2018-04-24 Gp Cellulose Gmbh Low viscosity kraft fiber having an enhanced carboxyl content and methods of making and using the same
US10138598B2 (en) 2013-03-14 2018-11-27 Gp Cellulose Gmbh Method of making a highly functional, low viscosity kraft fiber using an acidic bleaching sequence and a fiber made by the process
CN110468611A (en) * 2019-08-14 2019-11-19 岳阳林纸股份有限公司 A kind of PRC-APMP pulping process of Eucalyptus urophylla
US10865519B2 (en) 2016-11-16 2020-12-15 Gp Cellulose Gmbh Modified cellulose from chemical fiber and methods of making and using the same
US10907304B2 (en) 2005-05-02 2021-02-02 International Paper Company Ligno cellulosic materials and the products made therefrom
US11332886B2 (en) 2017-03-21 2022-05-17 International Paper Company Odor control pulp composition

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3597310A (en) * 1966-04-25 1971-08-03 Kokusaku Pulp Ind Co Ltd Method of producing high yield pulp by disc refining at ph of 12 to 14
EP0030778A1 (en) * 1979-12-17 1981-06-24 Q.N.S. Paper Company Limited Process for the formation of refiner pulp
WO1987003022A1 (en) * 1985-11-06 1987-05-21 Sunds Defibrator Aktiebolag Method of making mechanical pulp
WO1992020855A1 (en) * 1991-05-24 1992-11-26 Sunds Defibrator Industries Aktiebolag A method for the manufacture of chemithermomechanical pulp

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3597310A (en) * 1966-04-25 1971-08-03 Kokusaku Pulp Ind Co Ltd Method of producing high yield pulp by disc refining at ph of 12 to 14
EP0030778A1 (en) * 1979-12-17 1981-06-24 Q.N.S. Paper Company Limited Process for the formation of refiner pulp
WO1987003022A1 (en) * 1985-11-06 1987-05-21 Sunds Defibrator Aktiebolag Method of making mechanical pulp
WO1992020855A1 (en) * 1991-05-24 1992-11-26 Sunds Defibrator Industries Aktiebolag A method for the manufacture of chemithermomechanical pulp

Cited By (52)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0824160A1 (en) * 1996-08-14 1998-02-18 Giesecke & Devrient GmbH Process for the manufacture of paper making pulp
WO1999054544A1 (en) * 1998-04-17 1999-10-28 Alberta Research Council Inc. Method of producing lignocellulosic pulp from non-woody species
US6258207B1 (en) 1998-04-17 2001-07-10 Alberta Research Council Inc. Alkaline peroxide mechanical pulping of non-woody species
WO2000077301A1 (en) * 1999-06-15 2000-12-21 Kemira Chemicals Oy Method to improve the opacity of mechanical pulp by using aliphatic peroxyacids and use of peroxyacids to improve opacity
US8262850B2 (en) * 2003-09-23 2012-09-11 International Paper Company Chemical activation and refining of southern pine kraft fibers
WO2005045129A1 (en) * 2003-10-15 2005-05-19 Voith Paper Patent Gmbh Method for adjusting the ph and machine for preparing a fiber web
US10907304B2 (en) 2005-05-02 2021-02-02 International Paper Company Ligno cellulosic materials and the products made therefrom
JP2009529609A (en) * 2005-12-02 2009-08-20 アクゾ ノーベル ナムローゼ フェンノートシャップ Method for producing high yield pulp
US8268122B2 (en) 2005-12-02 2012-09-18 Akzo Nobel N.V. Process of producing high-yield pulp
NO339754B1 (en) * 2005-12-02 2017-01-30 Akzo Nobel Nv Process for producing high yield mass
AU2006321020B2 (en) * 2005-12-02 2011-02-10 Akzo Nobel Chemicals International B.V. Process of producing high-yield pulp
WO2007064287A1 (en) * 2005-12-02 2007-06-07 Akzo Nobel N.V. Process of producing high-yield pulp
WO2008132228A1 (en) * 2007-04-30 2008-11-06 Linde Aktiengesellschaft A method for reducing the energy consumption at the refining of a pulp suspension in a papermaking process and use of sodium bicarbonate in papermaking
US7993622B2 (en) 2007-05-04 2011-08-09 Kemira Oyj Method for preparing dithionite
WO2008135631A1 (en) * 2007-05-04 2008-11-13 Kemira Oyj Method for preparing dithionite
WO2009003770A1 (en) * 2007-07-03 2009-01-08 Linde Aktiengesellschaft Process for making paper and use of an acid/base treatment in papermaking
WO2010104725A1 (en) 2009-03-09 2010-09-16 Nalco Company Method and chemical composition to improve efficiency of mechanical pulp
US9512562B2 (en) 2009-05-28 2016-12-06 Gp Cellulose Gmbh Modified cellulose from chemical kraft fiber and methods of making and using the same
US10731293B2 (en) 2009-05-28 2020-08-04 Gp Cellulose Gmbh Modified cellulose from chemical kraft fiber and methods of making and using the same
USRE49570E1 (en) 2009-05-28 2023-07-04 Gp Cellulose Gmbh Modified cellulose from chemical kraft fiber and methods of making and using the same
US11111628B2 (en) 2009-05-28 2021-09-07 Gp Cellulose Gmbh Modified cellulose from chemical kraft fiber and methods of making and using the same
US10106927B2 (en) 2009-05-28 2018-10-23 Gp Cellulose Gmbh Modified cellulose from chemical kraft fiber and methods of making and using the same
US9970158B2 (en) 2009-05-28 2018-05-15 Gp Cellulose Gmbh Modified cellulose from chemical kraft fiber and methods of making and using the same
US9511167B2 (en) 2009-05-28 2016-12-06 Gp Cellulose Gmbh Modified cellulose from chemical kraft fiber and methods of making and using the same
US9512561B2 (en) 2009-05-28 2016-12-06 Gp Cellulose Gmbh Modified cellulose from chemical kraft fiber and methods of making and using the same
US9512237B2 (en) 2009-05-28 2016-12-06 Gp Cellulose Gmbh Method for inhibiting the growth of microbes with a modified cellulose fiber
US9926666B2 (en) 2009-05-28 2018-03-27 Gp Cellulose Gmbh Modified cellulose from chemical kraft fiber and methods of making and using the same
US9512563B2 (en) 2009-05-28 2016-12-06 Gp Cellulose Gmbh Surface treated modified cellulose from chemical kraft fiber and methods of making and using same
US9909257B2 (en) 2009-05-28 2018-03-06 Gp Cellulose Gmbh Modified cellulose from chemical kraft fiber and methods of making and using the same
US9777432B2 (en) 2009-05-28 2017-10-03 Gp Cellulose Gmbh Modified cellulose from chemical kraft fiber and methods of making and using the same
EP2443280A4 (en) * 2009-06-15 2014-08-13 Arkema Inc Alkaline peroxide treatment of rejects in an integrated neutral-alkaline paper mill
EP2443280A1 (en) * 2009-06-15 2012-04-25 Arkema, Inc. Alkaline peroxide treatment of rejects in an integrated neutral-alkaline paper mill
US8906198B2 (en) * 2012-11-02 2014-12-09 Andritz Inc. Method for production of micro fibrillated cellulose
US20150090412A1 (en) * 2012-11-02 2015-04-02 Andritz Inc. Process for production of micro fibrillated cellulose
US20140124150A1 (en) * 2012-11-02 2014-05-08 Andritz Inc. Method for production of micro fibrillated cellulose
US10138598B2 (en) 2013-03-14 2018-11-27 Gp Cellulose Gmbh Method of making a highly functional, low viscosity kraft fiber using an acidic bleaching sequence and a fiber made by the process
US9932709B2 (en) 2013-03-15 2018-04-03 Ecolab Usa Inc. Processes and compositions for brightness improvement in paper production
US9951470B2 (en) 2013-03-15 2018-04-24 Gp Cellulose Gmbh Low viscosity kraft fiber having an enhanced carboxyl content and methods of making and using the same
US10174455B2 (en) 2013-03-15 2019-01-08 Gp Cellulose Gmbh Low viscosity kraft fiber having an enhanced carboxyl content and methods of making and using the same
US10294614B2 (en) 2013-03-15 2019-05-21 Gp Cellulose Gmbh Low viscosity kraft fiber having an enhanced carboxyl content and methods of making and using the same
US10753043B2 (en) 2013-03-15 2020-08-25 Gp Cellulose Gmbh Low viscosity kraft fiber having an enhanced carboxyl content and methods of making and using the same
US10550516B2 (en) 2013-03-15 2020-02-04 Gp Cellulose Gmbh Low viscosity kraft fiber having an enhanced carboxyl content and methods of making and using the same
AU2015238642B2 (en) * 2014-03-25 2018-07-12 Basf Se Method for producing bleached wood fibre material
WO2015144455A1 (en) * 2014-03-25 2015-10-01 Basf Se Method for producing bleached wood fibre material
US11015290B2 (en) 2014-03-25 2021-05-25 Basf Se Method for producing bleached wood fibre material
EP2924166A1 (en) * 2014-03-25 2015-09-30 Basf Se Method for the manufacture of bleached wood fibre
CN106103842A (en) * 2014-03-25 2016-11-09 巴斯夫欧洲公司 The method producing bleaching wood fiber material
US11725338B2 (en) 2014-03-25 2023-08-15 Basf Se Method for producing bleached wood fibre material
US10865519B2 (en) 2016-11-16 2020-12-15 Gp Cellulose Gmbh Modified cellulose from chemical fiber and methods of making and using the same
US11332886B2 (en) 2017-03-21 2022-05-17 International Paper Company Odor control pulp composition
US11613849B2 (en) 2017-03-21 2023-03-28 International Paper Company Odor control pulp composition
CN110468611A (en) * 2019-08-14 2019-11-19 岳阳林纸股份有限公司 A kind of PRC-APMP pulping process of Eucalyptus urophylla

Also Published As

Publication number Publication date
AU4271596A (en) 1997-07-14

Similar Documents

Publication Publication Date Title
WO1997022749A1 (en) Process for treating refiner pulp
EP1095184B1 (en) Method of producing lignocellulosic pulp from non-woody species
US4798651A (en) Process for preparing pulp for paper making
US4431479A (en) Process for improving and retaining pulp properties
US20160024713A1 (en) Chemical activation and refining of southern pine kraft fibers
US6267841B1 (en) Low energy thermomechanical pulping process using an enzyme treatment between refining zones
EP1552052B1 (en) A method of producing mechanical pulp and the mechanical pulp thus produced
US4502918A (en) Two-stage chemical treatment of mechanical wood pulp with sodium sulfite
CA2634202C (en) Wood-based lignocellulosic fibrous material
EP0501059A1 (en) Steam explosion pulping process for papermaking
CA1112813A (en) Method for extracting ozone-treated fibrous materials
US5529663A (en) Delignification of lignocellulosic materials with peroxymonophosphoric acid
US3919041A (en) Multi-stage chlorine dioxide delignification of wood pulp
CA1173604A (en) Production of chemimechanical pulp
US6752904B2 (en) Process for removal of lignin from lignocellulosic material
CA1147909A (en) Method for delignifying and/or bleaching cellulose pulp
CA1320067C (en) Method of making mechanical and chemi-mechanical papermaking pulp
EP0096460B1 (en) Process for improving and retaining pulp properties
US4978426A (en) Production of high strength linerboard with oxygen and alkali
CA1170487A (en) Process for improving and retaining pulp properties
CA1309562C (en) Chemimechanical pulping process employing sodium carbonate and sodium sulphite
CA2399772A1 (en) Pulping process
CA1177607A (en) Chemical treatment of mechanical wood pulp
JPS6247999B2 (en)
EP0311356A1 (en) Process for bleaching mechanical pulp

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AU BR CA FI KR NO NZ SE US

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
122 Ep: pct application non-entry in european phase