NZ261328A - Production of chemi-thermomechanical pulp (ctmp) in which wood chips are first dipped in chemical reagents and are then mechanically defiberised using pressurised steam, the pulp then being refined; oxygen being added to the chips and/or raw pulp - Google Patents
Production of chemi-thermomechanical pulp (ctmp) in which wood chips are first dipped in chemical reagents and are then mechanically defiberised using pressurised steam, the pulp then being refined; oxygen being added to the chips and/or raw pulpInfo
- Publication number
- NZ261328A NZ261328A NZ261328A NZ26132894A NZ261328A NZ 261328 A NZ261328 A NZ 261328A NZ 261328 A NZ261328 A NZ 261328A NZ 26132894 A NZ26132894 A NZ 26132894A NZ 261328 A NZ261328 A NZ 261328A
- Authority
- NZ
- New Zealand
- Prior art keywords
- pulp
- oxygen
- process according
- chips
- ctmp
- Prior art date
Links
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21B—FIBROUS RAW MATERIALS OR THEIR MECHANICAL TREATMENT
- D21B1/00—Fibrous raw materials or their mechanical treatment
- D21B1/02—Pretreatment of the raw materials by chemical or physical means
- D21B1/021—Pretreatment of the raw materials by chemical or physical means by chemical means
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21B—FIBROUS RAW MATERIALS OR THEIR MECHANICAL TREATMENT
- D21B1/00—Fibrous raw materials or their mechanical treatment
- D21B1/04—Fibrous raw materials or their mechanical treatment by dividing raw materials into small particles, e.g. fibres
- D21B1/12—Fibrous raw materials or their mechanical treatment by dividing raw materials into small particles, e.g. fibres by wet methods, by the use of steam
- D21B1/14—Disintegrating in mills
- D21B1/16—Disintegrating in mills in the presence of chemical agents
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Paper (AREA)
Description
New Zealand Paient Spedficaiion for Paient Number £61 3£8 New Zealand No. 2 61328 International No. PCT/FR94/00138 TO BE ENTERED AFTER ACCEPTANCE AND PUBLICATION Priority dates; ^ \ ^ International fifing date: "J J *2) ;Classification: \Pc(o\ D2\&1) l(o ;Publication date: 2 In other words, the invention consists, during one of the two refining stages, primary or secondary, or even during these two phases, in introducing oxygen into the reaction medium. Preferably, oxygen is introduced during the 3 Sefibering stage, which is to say during primary refining while the reaction material is under a steam atmosphere under pressure, then the secondary refininc, is effected in known manner, particularly at atmospheric pressure.
The addition of oxygen into the reaction medium is known in the production of chemical pulps. The invention contemplates however introducing this oxygen into the production of CTMP pulps, at a precise point, namely during one of the refining phases and, preferably, during primary refining, and solely during this stage.
As a surprising result, the introduction of oxygen at the precise stage of defibering or primary re. tiling, in the absence of substantial air, into the chips already impregnated with chemical products, increases the synergetic effect of these products and permits on the one hand improving brightness and on the other hand and above all saving appreciably the energy necessary for defibering, while achieving a reduction in the weight of chemical reagents, during the bleaching phases of the ultimate pulps.
As is known, in the process for the production of CTMP, one begins generally with wood in the form of chips. Evergreen trees can be used as well as deciduous trees. These chips are then heated, particularly with steam, to permit homogenizing the humidity and temperature, and driving off air. In practice, this heating stage is effected in known manner at a temperature below 200°C, preferably between 110 and 160 °C. 4 Once heated, these chips are subjected to chemical impregnation, particularly by immersion or impregnation, with lignocellulosic reagents adapted to modify the lignin. In known manner, recourse is had to chemical reagents, particularly reducing agents, such as sodium sulfite, (Na2S03) , sodium bisulfite (Na2HS03) or sodium dithionite (NA2S204) . These compounds can be used alone or in combination with soda or sodium carbonate. As chemical reagents can also be mentioned oxidizing agents, such as hydrogen peroxide, preferably in alkaline medium, or percarbonates. This impregnation takes place also in known manner with saturated steam under pressure, at a temperature comprised between 8 0 and 140°C, preferably about 120°C. The CTMP's thus obtained are then washed, then classified to eliminate residual chemical reagents as well as the large particles of lignocellulosic material.
These pulps treated according to the process of the invention can eventually be bleached for example with hydrogen peroxide in alkaline material in one or several stages in the presence of soda and/or sodium hydrosulfite and complexing and stabilizing agents to achieve a high degree of brightness.
Preferably, in practice: - the oxygen is pure industrial oxygen, at a pressure greater than the pressure which prevails in the defibrator, and preferably at a pressure less than 10 bars, preferably at a pressure of 2 to 5 bars, and more generally about 3 bars; - the oxygen is introduced into the aperture of the defibrator, which is to say just upstream of the point at which the screw which provides the chips enters the stator; - the quantity of oxygen introduced is comprised between 1 to 5%, preferably between 1.5 and 2.5% by weight of the pulp (expressed as dry material).
In a surprising manner, the CTMP's treated in this way, have good physical and optical characteristics as well as improved brightness (from 2 to 5 points according to the base material used and the chemical reagents employed during impregnation. Moreover, the consumption of hydrogen peroxide during the ultimate bleaching stage of the pulp is, in a surprising manner, reduced by about 15%. Finally, the incorporation of oxygen at this stage of defibering, gives rise to a reduction of the consumption of energy necessary to drive the disks of defibrator, of the order of 10 to 25%, which translates to an appreciable gain because on an industrial scale, the electrical consumption of such a defibrator is frequently of the order of 10 to 15 kwh/ton. Finally, the pulp output is improved, which translates into a decrease of pollutants and the fibers have a better surface condition.
The manner in which the invention can be carried out and the advantages which follow from it, will become apparent from the examples of embodiment which follow with respect to the accompanying drawings. 2,u32& Figure 1 is a schematic view in cross section of a conventional so-called defibrator or primary refiner, for the production of CTMP's.
Figures 2-5 show the variation of different properties of the pulps treated according to the invention.
In the examples/ the following characteristics are measured: - length of rupture LR in meters (m) - index of resistance: IR Bursting x tearing - brightness Bl of the raw pulp in ISO % - pulp output (R in %) according to the standard NF Q03-002 according to standards NF Q03-053 NF Q03-011 according to the standard NF Q03-039 ratio of the weight of the dry pulp to the weight of the dry wood in % Unless otherwise indicated, these weight percentages are expressed relative to the dry pulp.
Example 1: Evergreen wood chips (epicea) are preheated to 110°C for 20 seconds, then heated while impregnating it with a solution of sodium sulfite of 100 g/1 to 125°C for ten minutes. These chips are then defibered in a disk defibrator under a relative pressure of 1.7 bar commonly used for the production of CTMP's shown in Figure 1. This defibrator comprises essentially a first body l heated if desired, in 7 2U3ZS which is introduced the chips 2 which advance under the influence of a rotating screw 3, to enter the inlet 4 of the defibrator itself 5, comprising a fixed stator 6 and a rotor 7 fixed to a shaft 8 coupled to a motor 10. The defibered pulp P leaves by the opening (11).
This pulp P is then washed and refined to a draining index of 100 ml CSF (standard CPPA - CI: 62 or SCAN-C21:65).
The characteristics of the obtained pulp are as follows: - LR: 4190 - IR: 48.8 - Bl: 58.8 - R : 92.8 Example 2: The defibrator of Figure 1 is modified by including a tubing (12) disposed adjacent the inlet 4, closed by a valve 13 connected to a source 14 of oxygen under pressure. The pulp treated with a quantity of oxygen of about 2.5% relative to the pulp and under a pressure of 5 bars, has the following characteristics: - LR: 3900 (as against 4190) - IR: 47.3 (as against 48.8) - Bl: 59.7 (as against 58.8) - R : 93.7 (as against 92.8).
Moreover, it is noted that the consumption of energy of the motor 10 is reduced by about a quarter, namely by about 250 kwh/ton. 8 ^U3ZS Example 3: In known manner, the two pulps of Examples l and 2 are bleached with 3% hydrogen peroxide, 3% soda, 3% sodium silicate, 0.3% DTPA (diethylene triamine penta-acetic acid), and 0.1% of magnesium sulfite. This bleaching is effected at a pulp concentration of 16% for three hours at 70°C.
With the pulp of Example 1, there is obtained a brightness of 75.5 and with the pulp of Example 2, a brightness of 77.0.
The gain of brightness observed in Example 2, is increased by a final stage of bleaching with hydrogen peroxide. Thus, to achieve the same brightness of 7 5.5 with the pulp of Example 1 treated with hydrogen peroxide, but with a pulp treated with oxygen according to Example 2, there is a saving of 8.7% of hydrogen peroxide, which amounts to a substantial saving.
Example 4: Example 1 is repeated with poplar chips by impregnating the chips in a mixture of sodium dithionite at 64.2 g/1 and soda of 20 g/1. The CTMP obtained has the following characteristics: - LR: 4460 - IR: 27.2 - Bl: 60.4 2. U 3 2-8 Example 5: Example 4 is repeated by including oxygen under pressure, according to Example 2 above. There are obtained the following characteristics: - LR: 4260 (as against 4460) - IR: 29.7 (as against 27.2) - Bl: 62 (as against 60.4) - R : 91.5 (as against 90.4).
The process according to the invention therefore permits improving the brightness by two points, increasing the output by one point and effecting a reduction of energy consumption for defibering, of about 15%.
After bleaching with hydrogen peroxide, under the same conditions as in Examples 3 and 4, there is observed a brightness of: - without oxygen: 79.4 - with oxygen: 80.0.
For the same brightness, the saving of hydrogen Example 6: Example 1 is repeated, but replacing the 100 g/1 of sodium sulfite by 82 g/1 of sodium bisulfite. There are obtained the following results: peroxide would be of the order of 3%.
Bl LR IR R Without Qxvaen 4500 35-9 54.2 91.7 With Qxvaen 4380 35.3 59. 0 92.2 / Ua l3 Zh It will thus be seen that there is an increase of brightness of 5 points with increased output of 0.5 point and a reduction of energy consumption during defibering in the presence of oxygen of 18%.
After bleaching, in a single step with 3% peroxide, the brightness improves from 75.6 to 78.0, namely a saving of hydrogen peroxide of 12%.
Example 7: There is introduced into the inlet of the defibrator 4, not only oxygen, but also a solution of hydrogen peroxide comprising 3% of peroxide and 2% of sodium carbonate, 2% of sodium silicate and 0.2% of DTPA. The reaction is allowed to proceed for about 30 minutes after defibering. There is obtained an increase of brightness of 0.5 point, an increase of output of one point and a noticeable improvement of the length of rupture LR (3800 as against 3130) and of the ♦ bursting index IR (32.7 as against 31.4).
There is moreover noted a reduction in the energy consumption of 20%.
After bleaching in a hydrogen peroxide step, there is observed an improvement of brightness of 1.6 point by incorporation of oxygen, which translates for the same level of brightness, into a saving of 10.7% of hydrogen peroxide.
Example 8: Example 7 is repeated, by impregnating however the epicea chips with a solution comprising: 11 -LU32& - hydrogen peroxide: 2% relative to the dry chips - sodium carbonate: 2% relative to the dry chips instead of 2% of sodium carbonate - sodium silicate: 2% relative to the dry chips - DTPA: 0.2% relative to the dry chips.
There are obtained the following characteristics: Without Oxygen With Qxvaen LR 3630 3530 IR 33.9 34.1 Bl 58.8 59.9 R 95.1 95.5 There is therefore observed a gain of brightness of one point, an output improved by 0.5 point, for identical pulp properties.
After bleaching with hydrogen peroxide, the brightness Bl increases from 75.5 for a process without oxygen to 77.5 in a process with oxygen, which, for a level of brightness of 75.5, permits a saving of 11.4% of hydrogen peroxide.
Example 9: Example 6 is repeated, using variable quantities of oxygen; the bleaching with peroxide is however not repeated.
The results obtained are shown in Figures 2-5, in which on the abscissa there is shown the quantity of oxygen introduced as a weight percent and on the respective ordi-nates: - in Figure 2, brightness Bl, 12 - in Figure 3, defibering energy in kwh/ton, - in Figure 4, the index of resistance Ir, - in Figure 5, the length of rupture LR in meters.
The brightness increases with the percentage of oxygen introduced. Beyond 2.5% oxygen, the gain of brightness stabilizes, but the surplus oxygen has a beneficial influence on the energy consumption in the defibering stage (the values correspond to the energy consumed by a primary refiner 3 0 cm in diameter). The rupture length and the index of resistance decrease linearly with the oxygen load. The rupture length decreases more quickly than the index of resistance.
As already said, the process according to the invention which consists in introducing selectively oxygen under pressure during mechanical defibering under an atmosphere of steam under pressure, has numerous advantages relative to the production processes for CTMP's known until now. There could be cited: - the fact that it is not necessary to modify the existing installations; - a gain of brightness Bl which can be as much as 5 points; - an appreciable energy saving for defibering or primary refining of the order of 10 to 2 5% according to the nature of the chemical reagents and of the wood chips used; - an appreciable reduction of the weight of chemical reagents, particularly of hydrogen peroxide in the final stages of treatment. 13
Claims (9)
1. Process for the production of chemi-thermomechanical pulps CTMP, which consists: first, in immersing wood chips in chemical reagents; - then mechanically defibering these chips (primary refining) under an atmosphere of steam under pressure, so as to obtain a raw pulp; and finally, refining said raw pulp (secondary refining), to obtain the CTMP, characterized in that during at least one of the two refining stages, oxygen is introduced into the reaction medium comprising said chips or said raw pulp.
2. Process according to claim 1, characterized in that the oxygen is introduced during the primary refining stage (mechanical defibering).
3. Process according to claim 1 or 2, characterized in that the oxygen is introduced at a pressure between 2 and 5 bars.
4. Process according to any one of claims 1 to 3, characterized in that the oxygen is introduced into the inlet of the defibrator. 14 261328
5. Process according to any one of claims 1 to 4, characterized in that the quantity of oxygen introduced is comprised between 1 and 5% by weight relative to the pulp (expressed as dry material).
6. Process according to any one of claims 1 to 5, characterized in that the chemical reagents are reducing agents alone or in mixture with soda or sodium carbonate. that the reducing agent is sodium sulfite, sodium bisulfite or sodium dithionite. characterized in that the chemical reagents are oxidizing agents. that the oxidizing agent is hydrogen peroxide or a percarbonate. 10. Process according to claim 9, characterized in that the hydrogen peroxide is used in an alkaline medium. 11. Process according to any one of claims 1 to 10, characterized in that after secondary refining, the CTMP is bleached. 12. Process for the production of chemi-thermomechanical pulps according to any one of claims 1 to 11, substantially as herein described.
7. Process according to claim 6, characterized in
8. Process according to any one of claims 1 to 5
9. Process according to claim 8, characterized in P obtained by the practice of the process CTte of claims 1 to 12. 15
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9301404A FR2701274B1 (en) | 1993-02-09 | 1993-02-09 | Process for the manufacture of bleached chemical thermal mechanical pulp (CTMP). |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NZ261328A true NZ261328A (en) | 1996-10-28 |
Family
ID=9443868
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ261328A NZ261328A (en) | 1993-02-09 | 1994-02-07 | Production of chemi-thermomechanical pulp (ctmp) in which wood chips are first dipped in chemical reagents and are then mechanically defiberised using pressurised steam, the pulp then being refined; oxygen being added to the chips and/or raw pulp |
Country Status (9)
| Country | Link |
|---|---|
| JP (1) | JPH07505930A (en) |
| BR (1) | BR9404036A (en) |
| CA (1) | CA2117799A1 (en) |
| DE (1) | DE4490578T1 (en) |
| FI (1) | FI944696A7 (en) |
| FR (1) | FR2701274B1 (en) |
| NZ (1) | NZ261328A (en) |
| SE (1) | SE9403227L (en) |
| WO (1) | WO1994018382A1 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2322020A1 (en) | 1998-02-18 | 1999-08-26 | Gmd - Forschungszentrum Informationstechnik Gmbh | Camera tracking system for a virtual television or video studio |
| CA2399772A1 (en) * | 2000-02-09 | 2001-08-16 | Akzo Nobel N.V. | Pulping process |
| FI122243B (en) * | 2009-03-17 | 2011-10-31 | Metso Paper Inc | Process and system for refining wood shavings or pulp fibers |
| CN105625074A (en) * | 2016-02-24 | 2016-06-01 | 张民贵 | Process for preparing pulp from hemp stems |
| WO2021110188A1 (en) * | 2019-12-03 | 2021-06-10 | Klingele Papierwerke Gmbh & Co. Kg | Method and device for producing fibrous material with a feed system and a helical screw system |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1277371A (en) * | 1960-10-19 | 1961-12-01 | Papeteries De Clairefontaine | Process and apparatus for the manufacture of pulp from sawmill waste |
| US4288288A (en) * | 1979-06-15 | 1981-09-08 | Weyerhaeuser Company | Apparatus for mixing chemicals into pulp at a refiner inlet |
| SE7905990L (en) * | 1979-07-10 | 1981-01-11 | Aga Ab | PROCEDURES FOR PREPARING PAPER Pulp |
| ZA837927B (en) * | 1983-05-23 | 1985-01-30 | Process Evaluation Devel | Thermomechanical digestion process using bleachants |
| SE454186C (en) * | 1985-03-13 | 1989-09-25 | Eka Nobel Ab | SET FOR PREPARATION OF CHEMICAL MECHANICAL |
| SE456430B (en) * | 1985-11-06 | 1988-10-03 | Sunds Defibrator | SET FOR MAKING MECHANICAL MASS |
-
1993
- 1993-02-09 FR FR9301404A patent/FR2701274B1/en not_active Expired - Fee Related
-
1994
- 1994-02-07 DE DE4490578T patent/DE4490578T1/en not_active Withdrawn
- 1994-02-07 CA CA002117799A patent/CA2117799A1/en not_active Abandoned
- 1994-02-07 FI FI944696A patent/FI944696A7/en unknown
- 1994-02-07 BR BR9404036A patent/BR9404036A/en not_active Application Discontinuation
- 1994-02-07 JP JP6517725A patent/JPH07505930A/en active Pending
- 1994-02-07 WO PCT/FR1994/000138 patent/WO1994018382A1/en not_active Ceased
- 1994-02-07 NZ NZ261328A patent/NZ261328A/en unknown
- 1994-09-26 SE SE9403227A patent/SE9403227L/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| BR9404036A (en) | 1999-06-01 |
| SE9403227D0 (en) | 1994-09-26 |
| JPH07505930A (en) | 1995-06-29 |
| DE4490578T1 (en) | 1995-04-13 |
| FI944696L (en) | 1994-11-22 |
| WO1994018382A1 (en) | 1994-08-18 |
| CA2117799A1 (en) | 1994-08-18 |
| FR2701274B1 (en) | 1995-03-31 |
| FR2701274A1 (en) | 1994-08-12 |
| FI944696A0 (en) | 1994-10-07 |
| FI944696A7 (en) | 1994-11-22 |
| SE9403227L (en) | 1994-09-26 |
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