EP0214982A1 - Verfahren zum bleichen von faserpulpe zur herstellung von papier und karton - Google Patents
Verfahren zum bleichen von faserpulpe zur herstellung von papier und kartonInfo
- Publication number
- EP0214982A1 EP0214982A1 EP19850902705 EP85902705A EP0214982A1 EP 0214982 A1 EP0214982 A1 EP 0214982A1 EP 19850902705 EP19850902705 EP 19850902705 EP 85902705 A EP85902705 A EP 85902705A EP 0214982 A1 EP0214982 A1 EP 0214982A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- pulp
- suspension
- base
- bleaching
- water
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 238000004061 bleaching Methods 0.000 title claims abstract description 43
- 238000000034 method Methods 0.000 title claims abstract description 40
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 5
- 239000000835 fiber Substances 0.000 title claims description 8
- 239000000725 suspension Substances 0.000 claims abstract description 59
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 55
- 239000011087 paperboard Substances 0.000 claims abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 29
- 238000001035 drying Methods 0.000 claims description 23
- 239000000126 substance Substances 0.000 claims description 20
- 239000007844 bleaching agent Substances 0.000 claims description 12
- 239000002245 particle Substances 0.000 claims description 9
- 150000002500 ions Chemical class 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 7
- 239000000843 powder Substances 0.000 claims description 6
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical class [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 claims description 5
- 239000001095 magnesium carbonate Substances 0.000 claims description 5
- 239000002023 wood Substances 0.000 claims description 5
- 230000000694 effects Effects 0.000 claims description 4
- 235000011160 magnesium carbonates Nutrition 0.000 claims description 4
- 239000000395 magnesium oxide Substances 0.000 claims description 4
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 4
- 235000012245 magnesium oxide Nutrition 0.000 claims description 4
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 4
- 239000000123 paper Substances 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
- 241000183024 Populus tremula Species 0.000 claims description 3
- 239000007900 aqueous suspension Substances 0.000 claims description 3
- 239000011121 hardwood Substances 0.000 claims description 3
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims description 3
- 239000000347 magnesium hydroxide Substances 0.000 claims description 3
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 2
- 239000003153 chemical reaction reagent Substances 0.000 claims description 2
- 150000002681 magnesium compounds Chemical class 0.000 claims description 2
- 238000002203 pretreatment Methods 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims description 2
- 239000007864 aqueous solution Substances 0.000 claims 2
- 235000019738 Limestone Nutrition 0.000 claims 1
- 241000219000 Populus Species 0.000 claims 1
- 239000006028 limestone Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 claims 1
- 239000007858 starting material Substances 0.000 claims 1
- 230000003068 static effect Effects 0.000 claims 1
- 150000002978 peroxides Chemical class 0.000 abstract description 13
- 239000003595 mist Substances 0.000 abstract description 2
- 239000011111 cardboard Substances 0.000 abstract 1
- 238000004076 pulp bleaching Methods 0.000 abstract 1
- 239000002585 base Substances 0.000 description 35
- 239000003513 alkali Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000000354 decomposition reaction Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 241000218657 Picea Species 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- HHSPVTKDOHQBKF-UHFFFAOYSA-J calcium;magnesium;dicarbonate Chemical class [Mg+2].[Ca+2].[O-]C([O-])=O.[O-]C([O-])=O HHSPVTKDOHQBKF-UHFFFAOYSA-J 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 230000005283 ground state Effects 0.000 description 1
- 238000009897 hydrogen peroxide bleaching Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C9/00—After-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
- D21C9/10—Bleaching ; Apparatus therefor
- D21C9/16—Bleaching ; Apparatus therefor with per compounds
- D21C9/163—Bleaching ; Apparatus therefor with per compounds with peroxides
Definitions
- This invention relates to a method of bleaching fibre pulps, which are obtained mechanically, chemi-mechanic ⁇ ally, che i-thermomechanically or semi-chemically from wood, especially hardwood, and are used for the making of paper or paperboard.
- the aforementioned types of pulps are bleach ⁇ ed in most cases by using hydrogen peroxide as bleaching agent.
- the bleaching is carried out normally as follows: The pulp resulting from one of the said defibering or digesting methods preferably first is washed more or less completely, in order to remove as completely as possible soluble substances originating from the raw material or pulp or obtained at the defibration.
- the pulp then is mixed with bleaching agents, especially hydrogen peroxide, alkali and sodium silicate, whereby the bleaching is initiated, which normally is carried out at pH 8 to 9 and at appr. 6 ⁇ °C.
- bleaching agents especially hydrogen peroxide, alkali and sodium silicate
- the processed susp ⁇ ension of the pulp in water then has a concentration of about 10 to 30$ by weight.
- the bleaching requires a reaction time of some hours.
- the pulp shall not contain large amounts of water- -soluble substances, which arose or were released at the pre-treatment.
- the bleaching shall be carried out at a high concen ⁇ tration of the pulp in water.
- the bleaching shall be carried out with a high per ⁇ oxide concentration.
- the bleaching shall be carried out in two steps. First a normal bleaching operation is carried out where- after the residual chemicals and the soluble substances resulting at the bleaching are removed by a washing. In a second step bleaching is then carried out with new chemicals.
- the present invention proposes a new bleaching method, which renders it possible to entirely eliminate the afore ⁇ said disadvantages.
- a suspens ⁇ ion of hydrogen peroxide is produced in air or water vapour, i.e. a suspension of a liquid as disperse phase in a gas as continuous phase, which means in principle it is a mist.
- air is preferred as continuous phase, because it is thereby possible to keep the temperature of the suspension very low until immediately before its mixing with the pulp suspension.
- hydrogen peroxide can be brought into direct contact with the pulp, without causing the per ⁇ oxide in the first place to meet too high a base concen ⁇ tration (too high a pH value) and to be decomposed there ⁇ by. A greater proportion of the hydrogen peroxide is then available for bleaching the pulp.
- the hydrogen peroxide can be combined in very high concentration with dry pulps and, consequently, this bleaching results in high, improved brightness degrees.
- the base is added in the form of a suspension to the dried pulp.
- the suspension of the base preferably is produced separately, so that peroxide and base do not meet unnecessarily early.
- a pref ⁇ erable step further is, not to mix the suspensions of peroxide and bases with each other in air or water vapour, before they are added to the pulp suspension.
- An improved contact and a more uniform absorption of the hydrogen peroxide by the pulp can be obtained by electro ⁇ statically charging the hydrogen peroxide suspension prior to i.ts admixture to the pulp.
- the charge must be suitable with respect to attraction to the particles of the pulp.
- the same step can be taken for admixing the base suspension, the particles of which are to be charged so that they have a charge opposed to the pulp particles containing hydrogen peroxide.
- an alkali hydroxide is used as base, in order to obtain the pH most favourable for the bleaching.
- a strong base at the high necessary concentrat ⁇ ions would cause a rapid premature decomposition of the hydrogen peroxide.
- a carbonate, or still better a bicarb ⁇ onate, of an alkali metal, especially sodium or ammonium is used. This step can be improved still more by using a difficultly soluble or a slowly soluble substance.
- difficultly soluble basic substances such are to be used which have a solubility lower than 0,015 g/100 g water at 20°C.
- Such difficultly soluble substances can be regarded to be especially magnesium hydroxide, magnesium oxide or basic magnesium carbonate.
- Magnesium carbonates and calcium-magnesium carbonates.- (dolomites) also can be used, but then the type to be used must be selected accurately, because the natural minerals in this combination often dissolve too slowly even in finest ground state.
- the natural calcium carbonates normally are too slowly soluble for being usable at this method.
- some qualities of chalk can be used which have a relatively very rapid dissolving rate.
- other bases can be used which have a higher solub ⁇ ility, for example up to 0,1 g/100 g water at 20°C. These bases, however, should dissolve relatively slowly, as a matter of fact so slowly, that when 1 g of the subst ⁇ ance is intensely stirred in 100 g of water at 8 ⁇ °C during two minutes the pH value of the suspension does not exceed the value of 9,5, especially 9,0.
- magnesium hydroxide basic magnesiu carbonates, magnesium oxide, magnesium carbonates or chalk with quick-soluble properties are suitable bases.
- two or more of the aforementioned bases can be combined with each other.
- a pH value of between 7,5 and 9,0, preferably a pH value between 7,8 and 8,5 is achieved.
- the present invention is based on the supply ' of hydrogen peroxide as suspension in air or water vapour to the suspension of the pulp dried and suspended in air or water vapour. This does not imply that also the base must be added entirely or partially after the drying of the pulp.
- the base on the contrary, can be added entire ⁇ ly or partially to the aqueous suspension of the pulp prior to its final dewatering and drying.
- the base in order to facilitate the redefibration at the papermaking it is advantageous to add part of the base necessary for bleaching prior to the drying of the pulp.
- basic substance enters also into the inner zones of the subsequently forming fibre aggregates.
- the pH is increased, the re- redefibration is facilitated, and the hydrogen peroxide, which subsequently by diffusion as liquid or gas enters into the interior of the aggregates, can even there have a bleaching effect due to the higher pH value.
- the suspensions of the reagents especially those of the hydrogen peroxide, after the drying of the pulp are added to its suspension in air or water vapour, whereby a rapid and uniform mixing with the pulp takes place.
- the pulp suspension in the place where other substances are added flows with high turbulence. This is achieved in that the pulp suspension is passed at high speed through a pipe. During the flow through this pipe, at least the peroxide suspension is admixed.
- the flow rate in the pipe should be at least 50 m/sec, preferably at least 150 m/sec.
- the suspension of the base can be introduced in the same pipe, or it can be added lateron to the pulp suspension, for example together with the cooling and transport air for the pulp suspension.
- the concentration of the pulp in suspension in the place where the peroxide suspension is added requires to be taken into regard. In a pulp suspension too concentrated, fibre flocculations or loose aggregates will form, which render a homogenous admixing of the peroxide difficult. According to the invention, it is advantageous when the pulp suspension contains at maximum 15 kg of dry pulp per cubic meter, preferably at maximum 8 kg/m and especially advantageously at maximum 5 kg/m .
- the invention can be applied with special advantage to pulps, which were obtained with a high yield of 80 to 95% from wood, calculated on dry matter. These pulp types normally often can be redefibred only with difficulty, after they have been dried, pressed and stored.
- the method according to the invention can also be the last step in a multi-step bleaching process.
- the steps preceding the bleaching according to the invention can be conventional bleaching processes in aqueous phase. By means of such bleaching methods comprising two or more steps a much stronger bleaching can be obtained,
- the wood chips was heated to 90°C, pressed and introd ⁇ uced into an alkaline sodium sulphite solution.
- the impregnation solution had a temperature of about 50°C.
- the chips was cooked for about 30 minutes with steam at atmospheric pressure. Thereafter it was defibred in two steps. The resulting pulp was washed in order to remove solved constituents. The pulp was then conventionally bleached, with 2% hydrog ⁇ en peroxide, 0,1$ complexing agent (DDPA), 3% sodium silicate and about 1% sodium hydroxide. The pulp was then at low concentration (about 1% ) cleaned of splint ⁇ ers and dewatered to a concentration of 5% » After a partial washing the pulp was dewatered to about 9% con ⁇ centration. At this point the method according to the invention commences. The 9% pulp suspension was intens ⁇ ively mixed with 1% finely ground chalk, calculated on the dry weight of the pulp.
- DDPA complexing agent
- the pulp suspension was thereafter transferred to cooling and drying air, the amount of which was about four times the weight of the pulp. In this cooling air about 0,8% by weight of magnesium oxide was suspended. This cooling and transporting air was then separated from the pulp in a cyclone. The pulp was pressed to bales and wrapped up.
- the pulp bleached according to the invention could after storage also be redefibrated more easily, compared with normally bleached pulp.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Paper (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH2384/84 | 1984-05-15 | ||
| CH238484 | 1984-05-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0214982A1 true EP0214982A1 (de) | 1987-03-25 |
Family
ID=4232515
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP19850902705 Withdrawn EP0214982A1 (de) | 1984-05-15 | 1985-05-15 | Verfahren zum bleichen von faserpulpe zur herstellung von papier und karton |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP0214982A1 (de) |
| AU (1) | AU4404285A (de) |
| WO (1) | WO1985005386A1 (de) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4400954B4 (de) * | 1994-01-14 | 2007-03-01 | Stefan Kürzeder | Verfahren zur Helligkeitssteigerung bei der Bleiche von Holzstoffen mit Wasserstoffperoxid |
| DE10211292A1 (de) | 2002-03-14 | 2003-09-25 | Basf Ag | Verfahren zur Herstellung von gefälltem Calciumcarbonat mit hohem Weißgrad |
| ES2806475T3 (es) * | 2016-04-15 | 2021-02-17 | Marinko MIKULIC | Un proceso continuo para la producción de pulpa de celulosa |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2492047A (en) * | 1946-03-30 | 1949-12-20 | Du Pont | Bleaching wood pulp |
| DE1546282A1 (de) * | 1965-10-16 | 1969-10-02 | Agricola Ind Per La Cellulosa | Verfahren und Anlage zum Bleichen von Zellulose |
| BE681488A (de) * | 1965-10-25 | 1966-10-31 | ||
| SE333498B (de) * | 1967-11-09 | 1971-03-15 | Sunds Ab | |
| SE324285B (de) * | 1968-11-22 | 1970-05-25 | T Norin | |
| SE362910B (de) * | 1972-06-13 | 1973-12-27 | Defibrator Ab |
-
1985
- 1985-05-15 WO PCT/SE1985/000206 patent/WO1985005386A1/en not_active Ceased
- 1985-05-15 AU AU44042/85A patent/AU4404285A/en not_active Abandoned
- 1985-05-15 EP EP19850902705 patent/EP0214982A1/de not_active Withdrawn
Non-Patent Citations (1)
| Title |
|---|
| See references of WO8505386A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| AU4404285A (en) | 1985-12-13 |
| WO1985005386A1 (en) | 1985-12-05 |
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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 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT DE FR GB SE |
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| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
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| 18D | Application deemed to be withdrawn |
Effective date: 19870120 |