CA2031972A1 - Procedure for the production of pulp - Google Patents
Procedure for the production of pulpInfo
- Publication number
- CA2031972A1 CA2031972A1 CA002031972A CA2031972A CA2031972A1 CA 2031972 A1 CA2031972 A1 CA 2031972A1 CA 002031972 A CA002031972 A CA 002031972A CA 2031972 A CA2031972 A CA 2031972A CA 2031972 A1 CA2031972 A1 CA 2031972A1
- Authority
- CA
- Canada
- Prior art keywords
- pulp
- oxidizing
- chemical
- lignin
- fibrous product
- 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.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 25
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 17
- 239000000126 substance Substances 0.000 claims abstract description 26
- 229920001131 Pulp (paper) Polymers 0.000 claims abstract description 22
- 239000011230 binding agent Substances 0.000 claims abstract description 19
- 108090000790 Enzymes Proteins 0.000 claims abstract description 18
- 102000004190 Enzymes Human genes 0.000 claims abstract description 18
- 230000001590 oxidative effect Effects 0.000 claims abstract description 16
- 229920005610 lignin Polymers 0.000 claims abstract description 12
- 230000002255 enzymatic effect Effects 0.000 claims abstract description 6
- OSVXSBDYLRYLIG-UHFFFAOYSA-N dioxidochlorine(.) Chemical compound O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 claims description 24
- 229920002472 Starch Polymers 0.000 claims description 14
- 235000019698 starch Nutrition 0.000 claims description 14
- 239000008107 starch Substances 0.000 claims description 14
- 239000004155 Chlorine dioxide Substances 0.000 claims description 12
- 235000019398 chlorine dioxide Nutrition 0.000 claims description 12
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 108010029541 Laccase Proteins 0.000 claims description 7
- 108010054320 Lignin peroxidase Proteins 0.000 claims description 4
- 108010059896 Manganese peroxidase Proteins 0.000 claims description 4
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims description 4
- 102000004169 proteins and genes Human genes 0.000 claims description 4
- 108090000623 proteins and genes Proteins 0.000 claims description 4
- 125000002091 cationic group Chemical group 0.000 claims description 3
- 150000002500 ions Chemical class 0.000 claims description 3
- 235000014633 carbohydrates Nutrition 0.000 claims description 2
- 150000001720 carbohydrates Chemical class 0.000 claims description 2
- 230000003647 oxidation Effects 0.000 claims description 2
- 238000007254 oxidation reaction Methods 0.000 claims description 2
- 229940088598 enzyme Drugs 0.000 claims 7
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims 1
- 102000003992 Peroxidases Human genes 0.000 claims 1
- 229910001448 ferrous ion Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 229940072417 peroxidase Drugs 0.000 claims 1
- 108040007629 peroxidase activity proteins Proteins 0.000 claims 1
- 239000000835 fiber Substances 0.000 abstract description 7
- 239000002023 wood Substances 0.000 description 12
- 238000004458 analytical method Methods 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000000123 paper Substances 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- 238000007670 refining Methods 0.000 description 4
- 239000001888 Peptone Substances 0.000 description 3
- 108010080698 Peptones Proteins 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 235000019319 peptone Nutrition 0.000 description 3
- 241000446313 Lamella Species 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 239000011111 cardboard Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 238000010297 mechanical methods and process Methods 0.000 description 2
- 239000011087 paperboard Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- IUQJDHJVPLLKFL-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)acetate;dimethylazanium Chemical compound CNC.OC(=O)COC1=CC=C(Cl)C=C1Cl IUQJDHJVPLLKFL-UHFFFAOYSA-N 0.000 description 1
- 102100031260 Acyl-coenzyme A thioesterase THEM4 Human genes 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000222356 Coriolus Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 229920002488 Hemicellulose Polymers 0.000 description 1
- 101000638510 Homo sapiens Acyl-coenzyme A thioesterase THEM4 Proteins 0.000 description 1
- 229940099408 Oxidizing agent Drugs 0.000 description 1
- 229920002522 Wood fibre Polymers 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000007767 bonding agent Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000007979 citrate buffer Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 229940070376 protein Drugs 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
- D21H11/08—Mechanical or thermomechanical pulp
-
- 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
- D21C3/00—Pulping cellulose-containing materials
- D21C3/006—Pulping cellulose-containing materials with compounds not otherwise provided for
-
- 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
- D21C5/00—Other processes for obtaining cellulose, e.g. cooking cotton linters ; Processes characterised by the choice of cellulose-containing starting materials
- D21C5/005—Treatment of cellulose-containing material with microorganisms or enzymes
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- Paper (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
( 57 ) ABSTRACT OF DISCLOSURE
The invention relates to a procedure for the production of mechanical pulp from a fibrous product. To improve the strength properties, the fibrous product is sub-jected to a chemical and/or enzymatic treatment in which a binding agent is linked with the lignin in the fibrous product. The bond between the binding agent and the fibre is created either by using oxidizing enzymes or oxidizing chemicals producing radicals.
The invention relates to a procedure for the production of mechanical pulp from a fibrous product. To improve the strength properties, the fibrous product is sub-jected to a chemical and/or enzymatic treatment in which a binding agent is linked with the lignin in the fibrous product. The bond between the binding agent and the fibre is created either by using oxidizing enzymes or oxidizing chemicals producing radicals.
Description
2~31~37~
PROCEDURE FOR THE PRODUCTION OF PULP
The present invention relates to a procedure for the pro-duction of mechanical pulp from a fibrous product.
The production of mechanical pulp from a fibrous product, such as whole wood, wood chi~ps, chips or refined pulp is mainly implemented by mechanical methods. The production of mechanical pulp is based on the utilization o~ friction.
Energy is transferred to thle wood in a compress-release process generating frictional heat which soften~ the wood so that individual fibres can be released.
The object of pulp production is to reduce the wood struc-ture into fibres and to process the fibres so as to make them fit for use as raw material in the manufacture of paper or cardboard. The natural function of wood fibres is exactly the opposite of this object, i.e. to form a supporting structure as strong as possible.
The fibres are bound together by an intermediate lamella which mainly consists of lignin. In the manufacture of chemical pulp, the intermediate lamella i5 dissolved using chemicals. The fibres can be separated undamaged, but besides lignin, even some of the hemicellulose in the wood is dissolved. Only about half the fibre content of the wood can be retrieved, i.e. the yield is 50 %. In mechanical methods, the lignin is softened by means of water, heat and repeated application of mechanical stress so that the fibres can be "torn" apart. The fibres are disrupted in the process, but the yield is as high as 96-98~.
Mechanical pulps are produced by separating the fibres, which are bound together in the wood, either by grinding the wood against a grinding stone or by refining wood chips in disc refiners. The former type of pulp is generally ~,~3~72 called groundwood pulp and the latter type is called refiner mechanical pulp. In the more advanced forms of the refining method, heat (TMP~ and possibly even chemicals (CTMP) are used.
The yield in the mechanical pulp production methods is high. Only a few per cent of the weight of the wood is lost. Therefore, the cost oE the wood as per ton of pulp is low. On the other hand, the energy consumption is high, and the energy costs are an important factor. Also, the vigor-ous mechanical treatment causes fibre damage, reducing the strength of the paper produced from the pulp, which is why the use of mechanical pulp is limited to certain products of a lower quality requirement level.
In earlier research it has been established that the strength properties of mechanical pulp can be influenced by the degree of refining and by mechanically adding binding agents or softwood sulphate pulp into the mechanical pulp.
Increasing the degree of refining involves the disadvan-tages of increased production costs and a low processabili-ty (anhydrou~ quality~ of the refined product. Adding sulphate pulp into mechanical pulp is generally avoided as far as possible because of the costs.
Binding agents are used to strengthen the bonds between the fibras. The strength properties of paper are largely dependent on these bonds. By far the most commonly used dry strength bonding agent is cationic starch. For wood pulps with a high content of fine fibres and fillers, the amount of starch needed is 0.5 - 2 ~. If starch is used in amounts exceeding this, the operability of the machine as well as the paper ~uality practically always decline.
Thus, the object of the present invention is to create a procedure by which the strength properties of mechanical .', 3 ~, ~ 3 ~
pulp can be improved. The invention is characterized in that the fibrous product is subjected to a chemical and/or enzymatic treatment in which a binding agent is linked with the lignin in the fibrous product. According to the inven-tion, it has been established that, by using an enzyme and/or a chemical, it is possible to add a suitable mol-ecule to the free and easily oxidizable groups of lignin.
If a binding agent is united with the fibre surface in a chemical reaction, it will improve the strength properties of the fibre. I~ necessary, the amount of binding agent used can be increased without producing adverse effects.
The bond between the binding agent and the fibre is created either by using oxidi~ing enzymes or oxidizing chemicals producing radicals.
The strength properties can be improved with an enzyme treatment in which mechanical pulp is treated in the pres~
ence of certain substances, e.g. carbohydrates and pro-teins, containing hydrophilic groups, with enzymes acting on lignin. Chemical bonding can be successfully achieved in mechanical pulps produced by different methods on condition that liynin or its derivatives are present in the reaction mixture.
The purpose of the oxidation treatment, either enzymatic or chemical, is to produce in the lignin of the fibre a radi-cal with which the binding agent is linked by a chemical bond so that the stren~th properties of the pulp are sub-stantially improved. The substance used for producing a radical is preferably laccase, lignin peroxidase, manganese peroxidase or an oxidizing chemical producing radicals, e.g. chlorine dioxide, ozone or hydrogen peroxide together with ferro ions. Examples of suitable enzymes are those produced by white rot fungi, e.g. the lacrase produced by the fungus Coriolus versiculum. The pulp temperature during the ezyme treatment may be in the range 10-90C, preferably 40-70C, and the pH in the range 2.0-10.0, preferably 2 ~ ?~
PROCEDURE FOR THE PRODUCTION OF PULP
The present invention relates to a procedure for the pro-duction of mechanical pulp from a fibrous product.
The production of mechanical pulp from a fibrous product, such as whole wood, wood chi~ps, chips or refined pulp is mainly implemented by mechanical methods. The production of mechanical pulp is based on the utilization o~ friction.
Energy is transferred to thle wood in a compress-release process generating frictional heat which soften~ the wood so that individual fibres can be released.
The object of pulp production is to reduce the wood struc-ture into fibres and to process the fibres so as to make them fit for use as raw material in the manufacture of paper or cardboard. The natural function of wood fibres is exactly the opposite of this object, i.e. to form a supporting structure as strong as possible.
The fibres are bound together by an intermediate lamella which mainly consists of lignin. In the manufacture of chemical pulp, the intermediate lamella i5 dissolved using chemicals. The fibres can be separated undamaged, but besides lignin, even some of the hemicellulose in the wood is dissolved. Only about half the fibre content of the wood can be retrieved, i.e. the yield is 50 %. In mechanical methods, the lignin is softened by means of water, heat and repeated application of mechanical stress so that the fibres can be "torn" apart. The fibres are disrupted in the process, but the yield is as high as 96-98~.
Mechanical pulps are produced by separating the fibres, which are bound together in the wood, either by grinding the wood against a grinding stone or by refining wood chips in disc refiners. The former type of pulp is generally ~,~3~72 called groundwood pulp and the latter type is called refiner mechanical pulp. In the more advanced forms of the refining method, heat (TMP~ and possibly even chemicals (CTMP) are used.
The yield in the mechanical pulp production methods is high. Only a few per cent of the weight of the wood is lost. Therefore, the cost oE the wood as per ton of pulp is low. On the other hand, the energy consumption is high, and the energy costs are an important factor. Also, the vigor-ous mechanical treatment causes fibre damage, reducing the strength of the paper produced from the pulp, which is why the use of mechanical pulp is limited to certain products of a lower quality requirement level.
In earlier research it has been established that the strength properties of mechanical pulp can be influenced by the degree of refining and by mechanically adding binding agents or softwood sulphate pulp into the mechanical pulp.
Increasing the degree of refining involves the disadvan-tages of increased production costs and a low processabili-ty (anhydrou~ quality~ of the refined product. Adding sulphate pulp into mechanical pulp is generally avoided as far as possible because of the costs.
Binding agents are used to strengthen the bonds between the fibras. The strength properties of paper are largely dependent on these bonds. By far the most commonly used dry strength bonding agent is cationic starch. For wood pulps with a high content of fine fibres and fillers, the amount of starch needed is 0.5 - 2 ~. If starch is used in amounts exceeding this, the operability of the machine as well as the paper ~uality practically always decline.
Thus, the object of the present invention is to create a procedure by which the strength properties of mechanical .', 3 ~, ~ 3 ~
pulp can be improved. The invention is characterized in that the fibrous product is subjected to a chemical and/or enzymatic treatment in which a binding agent is linked with the lignin in the fibrous product. According to the inven-tion, it has been established that, by using an enzyme and/or a chemical, it is possible to add a suitable mol-ecule to the free and easily oxidizable groups of lignin.
If a binding agent is united with the fibre surface in a chemical reaction, it will improve the strength properties of the fibre. I~ necessary, the amount of binding agent used can be increased without producing adverse effects.
The bond between the binding agent and the fibre is created either by using oxidi~ing enzymes or oxidizing chemicals producing radicals.
The strength properties can be improved with an enzyme treatment in which mechanical pulp is treated in the pres~
ence of certain substances, e.g. carbohydrates and pro-teins, containing hydrophilic groups, with enzymes acting on lignin. Chemical bonding can be successfully achieved in mechanical pulps produced by different methods on condition that liynin or its derivatives are present in the reaction mixture.
The purpose of the oxidation treatment, either enzymatic or chemical, is to produce in the lignin of the fibre a radi-cal with which the binding agent is linked by a chemical bond so that the stren~th properties of the pulp are sub-stantially improved. The substance used for producing a radical is preferably laccase, lignin peroxidase, manganese peroxidase or an oxidizing chemical producing radicals, e.g. chlorine dioxide, ozone or hydrogen peroxide together with ferro ions. Examples of suitable enzymes are those produced by white rot fungi, e.g. the lacrase produced by the fungus Coriolus versiculum. The pulp temperature during the ezyme treatment may be in the range 10-90C, preferably 40-70C, and the pH in the range 2.0-10.0, preferably 2 ~ ?~
4.0-8Ø In addition, the redox potential must be relative-ly high, in enzyme treatment approx. 100-600 mV, preferably 300-500 mV, and in chemical treatment above 200 mV.
In the following, the invention is described in detail by the aid of examples of embodiments based on laboratory tests.
Example 1.
g (ahs.k) of reclaimed paper pulp made of reclaimed paper and cardboard was diluted with water until à
consistency of 2.5 %. was reached.
The mixture was heated to 40C. Next, starch (Amisol 202) in an amount of 5 % was added into the mixture, which was stirred properly. Water-diluted chlorine dioxide in a quantity of 0.5 % of the amount of pulp was added into the reaction mixture. The reaction was allowed to continue at 40C for two hours.
After this, the pulp was washed with a 20-fold amount of water, whereupon it was concentrated and analyzed.
The results reflecting the strength of the pulp are presented in Table 1.
In addition to the test described above (test 5), three reference tests (tests 1, 2 and 3) and two additional tests (tests 4 and 6) were carried out. The results of these are likewise presented in Table 1. The tests were performed as follo~s:
', :::
.
.
'~ ` ' ;""' ~D
E~ u~ o ~ ~ I~ , ~q E~
u~ o E~
Ul o Ir) ~1~ ~) O N
:-1 _ _ _ ~r E~ ~ ~ ~ o O O ~ U~
C
O ~ I`
E~ ~ o o U~ ~ ,_ o U~
~ -_ , ~ ~~ ~ ~0 E~ ~ o u~ .. .
~n ~u ~u~
E~ h a~
~ o~ r-E~ U~ o o v~ ~u ~
E~ ~
_ _ N ~
a~ 1 h o ~ a x ~ ~a -- Q~ ~ ~ O U~
~ ~ rl a~ u Q~ a -- --I q-l . .~: g"11 u~ (~1 ~ ~1 O ~ O
~I Q~ h ~ h ~ r1 p~ v O ~ ~ 0 Ul -rl ~1 ri q~ ~rl O d~ ~ VJ ~ N ,S~
dP ~) O
_ .~ ~ h t~ X C ~ O h N ~ ~ O O
~ c~ ~ C ~
: ~ - ~) O ~ :~:O ~ ~) O dP ~ O O C C:
~ ~ W r~ O
~ ~3 `, , ` ~ . , , . ~, .. .. .. .
:- : .,, ' 6 ~ r~ ~
Test 1 (reEerence): The pulp was not treated with chlorine dioxide and no starch was added to it. In other respect~
the implementation and analysis of the test corresponded to the test described abov2 (test 5).
Test 2 (reference): No chlorine dioxide treatment of the pulp wa~ performed. In other respects the implementation and analysis of the test corresponded to the test described above (test 5).
Test 3 (reference): ~o chlorine dioxide treatmen~ was performed. Starch was added to the pulp in an amount of 10 ~ of the amount of pulp.
Test 4: The pulp was treated with chlorine dio~ide, hut no starch was added. In other respects the implementation and analysis of the test correspond~d to the test described above (test 5). The procedure represented by this test belongs to the sphere of the present invention.
Test 6: The pulp was treated with chlorine dioxide after a starch addition of 10 % of the amount of pulp. In other respects the implementation and analysis of the test corresponded to the test described above (test 5). The procedure represented by this test belongs to the sphere of the present invention.
'.
Example 2.
Unbleached TMP pulp was washed with ion-exchanged water and centrifugalized. The pulp was buffered with a Na citrate buffer, diluted to a consistency of 2.5 % and heated to 40 C. Starch (oxidized, medium cationic) was added to the pulp in an amount of 5 %, and the pulp was stirr~d proper-ly. Laccase (activity 630 U/ml) diluted with water was added to the mixture in an amount of 0.1 % of the amount of mixture, and the pulp was stirred carefully. The enzymatic : , .
.
' .
.
reaction was allowed to continue for two hours at a tem-perature of 40 C. The pulp was stirred periodically during this time. At the end of the reaction the pulp was washed.
After the washing, the enzyme activity was destroyed by a 10-minute heat treatment at S0-85 C. Finally, the pulp was concentrated, centrifugalized and homogenized.
100 g sheets 1SCAN-67) were produced from the pulps, and the sheets were tumble dried. The paper technical proper-ties of the sheets were determined in accordance with the SCAN standards.
The results reflecting the strength of the pulp are presented in Tabl~ 2.
In addition to the test described above (test 2), a refer-ence test (test 1) and two additional tests (tests 3 and 4) were carried out. The results of these are likewise pre-sented in Table 1. The tests were performed as follows:
Test 1 (reference): The pulp was not subjected to an enzyme treatment and no starch was added to it. As for the washing of the pulp and the analyses, the test corresponded to that described above (test 2).
Test 3: The pulp was subjected to an enzyme treatment after peptone, instead of starch, in an amount of 5 % of the amount of pulp had been added into the reaction solution.
In all other respects, the treatment corresponded to that described above (test 2). The procedure represented by this test belongs to the sphere of the present invention.
Test 4: Instead of an enzyme treatment, the pulp was sllbjected to an oxidizing chlorine dioxide treatment. The amount of chlorine dioxide used was 0.1 % of the amount of pulp. In all other respects, the treatment corresponded to ....... .
~ ` . .
:. . '' ' ,-: ' ;
' , c~ 2 that described above (test 2). The proc-edure represented by this test belongs to the sphere of the present invention.
It is obvious from the results that the strength can be increased in the same way regardless of whether the oxidiz-ing agent is chlorine dioxide or laccase. The results also indicate that, besides starch, peptone, too, can be used together with an oxidizing treatment to increase the strength of the pulp.
It can be seen from the results that the mere addition of starch as a binding agent increased the strength as ex-pected, but the increase in strength was clearly larger in the cases where the pulp had been subjected to an oxidizing treatment as provided by the invention.
It is obvious to a person skilled in the art that the invention is not restricted to the embodiment example described above, but that it may instead be varied within the scope of the followirlg claims.
(reference) Laccase % of pulp _ 0.1 0.1 C102 ~ of pulp _ ~ 0.1 Starch % of pulp _ 5 _ 5 Peptone ~ of pulp _ _ 5 Freeness CSF (ml) 40 39 30 45 Tensile index Nm/g 44.6 55.0 53.3 54.0 Increase in strength (~) 23.3 19.521.1 _ ., . " . " .. ~ . .. . . .. .. .
, ' :, :
In the following, the invention is described in detail by the aid of examples of embodiments based on laboratory tests.
Example 1.
g (ahs.k) of reclaimed paper pulp made of reclaimed paper and cardboard was diluted with water until à
consistency of 2.5 %. was reached.
The mixture was heated to 40C. Next, starch (Amisol 202) in an amount of 5 % was added into the mixture, which was stirred properly. Water-diluted chlorine dioxide in a quantity of 0.5 % of the amount of pulp was added into the reaction mixture. The reaction was allowed to continue at 40C for two hours.
After this, the pulp was washed with a 20-fold amount of water, whereupon it was concentrated and analyzed.
The results reflecting the strength of the pulp are presented in Table 1.
In addition to the test described above (test 5), three reference tests (tests 1, 2 and 3) and two additional tests (tests 4 and 6) were carried out. The results of these are likewise presented in Table 1. The tests were performed as follo~s:
', :::
.
.
'~ ` ' ;""' ~D
E~ u~ o ~ ~ I~ , ~q E~
u~ o E~
Ul o Ir) ~1~ ~) O N
:-1 _ _ _ ~r E~ ~ ~ ~ o O O ~ U~
C
O ~ I`
E~ ~ o o U~ ~ ,_ o U~
~ -_ , ~ ~~ ~ ~0 E~ ~ o u~ .. .
~n ~u ~u~
E~ h a~
~ o~ r-E~ U~ o o v~ ~u ~
E~ ~
_ _ N ~
a~ 1 h o ~ a x ~ ~a -- Q~ ~ ~ O U~
~ ~ rl a~ u Q~ a -- --I q-l . .~: g"11 u~ (~1 ~ ~1 O ~ O
~I Q~ h ~ h ~ r1 p~ v O ~ ~ 0 Ul -rl ~1 ri q~ ~rl O d~ ~ VJ ~ N ,S~
dP ~) O
_ .~ ~ h t~ X C ~ O h N ~ ~ O O
~ c~ ~ C ~
: ~ - ~) O ~ :~:O ~ ~) O dP ~ O O C C:
~ ~ W r~ O
~ ~3 `, , ` ~ . , , . ~, .. .. .. .
:- : .,, ' 6 ~ r~ ~
Test 1 (reEerence): The pulp was not treated with chlorine dioxide and no starch was added to it. In other respect~
the implementation and analysis of the test corresponded to the test described abov2 (test 5).
Test 2 (reference): No chlorine dioxide treatment of the pulp wa~ performed. In other respects the implementation and analysis of the test corresponded to the test described above (test 5).
Test 3 (reference): ~o chlorine dioxide treatmen~ was performed. Starch was added to the pulp in an amount of 10 ~ of the amount of pulp.
Test 4: The pulp was treated with chlorine dio~ide, hut no starch was added. In other respects the implementation and analysis of the test correspond~d to the test described above (test 5). The procedure represented by this test belongs to the sphere of the present invention.
Test 6: The pulp was treated with chlorine dioxide after a starch addition of 10 % of the amount of pulp. In other respects the implementation and analysis of the test corresponded to the test described above (test 5). The procedure represented by this test belongs to the sphere of the present invention.
'.
Example 2.
Unbleached TMP pulp was washed with ion-exchanged water and centrifugalized. The pulp was buffered with a Na citrate buffer, diluted to a consistency of 2.5 % and heated to 40 C. Starch (oxidized, medium cationic) was added to the pulp in an amount of 5 %, and the pulp was stirr~d proper-ly. Laccase (activity 630 U/ml) diluted with water was added to the mixture in an amount of 0.1 % of the amount of mixture, and the pulp was stirred carefully. The enzymatic : , .
.
' .
.
reaction was allowed to continue for two hours at a tem-perature of 40 C. The pulp was stirred periodically during this time. At the end of the reaction the pulp was washed.
After the washing, the enzyme activity was destroyed by a 10-minute heat treatment at S0-85 C. Finally, the pulp was concentrated, centrifugalized and homogenized.
100 g sheets 1SCAN-67) were produced from the pulps, and the sheets were tumble dried. The paper technical proper-ties of the sheets were determined in accordance with the SCAN standards.
The results reflecting the strength of the pulp are presented in Tabl~ 2.
In addition to the test described above (test 2), a refer-ence test (test 1) and two additional tests (tests 3 and 4) were carried out. The results of these are likewise pre-sented in Table 1. The tests were performed as follows:
Test 1 (reference): The pulp was not subjected to an enzyme treatment and no starch was added to it. As for the washing of the pulp and the analyses, the test corresponded to that described above (test 2).
Test 3: The pulp was subjected to an enzyme treatment after peptone, instead of starch, in an amount of 5 % of the amount of pulp had been added into the reaction solution.
In all other respects, the treatment corresponded to that described above (test 2). The procedure represented by this test belongs to the sphere of the present invention.
Test 4: Instead of an enzyme treatment, the pulp was sllbjected to an oxidizing chlorine dioxide treatment. The amount of chlorine dioxide used was 0.1 % of the amount of pulp. In all other respects, the treatment corresponded to ....... .
~ ` . .
:. . '' ' ,-: ' ;
' , c~ 2 that described above (test 2). The proc-edure represented by this test belongs to the sphere of the present invention.
It is obvious from the results that the strength can be increased in the same way regardless of whether the oxidiz-ing agent is chlorine dioxide or laccase. The results also indicate that, besides starch, peptone, too, can be used together with an oxidizing treatment to increase the strength of the pulp.
It can be seen from the results that the mere addition of starch as a binding agent increased the strength as ex-pected, but the increase in strength was clearly larger in the cases where the pulp had been subjected to an oxidizing treatment as provided by the invention.
It is obvious to a person skilled in the art that the invention is not restricted to the embodiment example described above, but that it may instead be varied within the scope of the followirlg claims.
(reference) Laccase % of pulp _ 0.1 0.1 C102 ~ of pulp _ ~ 0.1 Starch % of pulp _ 5 _ 5 Peptone ~ of pulp _ _ 5 Freeness CSF (ml) 40 39 30 45 Tensile index Nm/g 44.6 55.0 53.3 54.0 Increase in strength (~) 23.3 19.521.1 _ ., . " . " .. ~ . .. . . .. .. .
, ' :, :
Claims (15)
1. Procedure for the production of mechanical pulp from a fibrous product, c h a r a c t e r i z e d in that the fibrous product is subjected to a chemical and/or enzymatic treatment in which a binding agent is linked with the lignin in the fibrous product.
2. Procedure according to claim 1, c h a r a c t e r -i z e d in that, during the chemical and/or enzymatic treatment of the fibrous product, radicals are produced in the lignin in the fibrous product, the binding agents being linked with the radicals by chemical bonds.
3. Procedure according to claim 1 or 2, c h a r a c t e r -i z e d in that the binding agent is a hydrophilic substance, preferably a hydrocarbonate and/or a protein.
4. Procedure according to any one of the preceding claims, c h a r a c t e r i z e d in that the substance used for producing a radical is an oxidizing enzyme and/or an oxidizing chemical producing radicals, preferably laccase, lignin peroxidase, manganese peroxidase, hydrogen peroxide together with ferro ions, chlorine dioxide or ozone, used either by themselves or in mixtures.
5. Procedure according to any one of the preceding claims, c h a r a c t e r i z e d in that the enzyme treatment is performed within a temperature range of 10-90°C, preferably 40-70°C, and at a pH of 2.0-10.0, preferably 4.0 8Ø
6. Use of enzymes and/or chemicals acting on lignin, together with binding agents, to increase the strength properties of pulp in the manufacture of mechanical pulp.
7. Use of an enzyme and/or chemical according to claim 6 to improve the strength properties in the manufacture of mechanical pulp when oxidizing enzymes and/or oxidizing chemicals producing radicals are used.
8. Use of a binding agent according to claim 6 to improve the strength properties in the manufacture of mechanical pulp, the binding agents used being preferably hydrocarbonates and/or proteins.
9. Use of laccase, lignin peroxidase, manganese per-oxidase, hydrogen peroxidase together with ferro ions, chlorine dioxide, ozone or mixtures of these according to claim 6 to improve the strength properties in the manufacture of mechanical pulp .
10. A process for the production of mechanical pulp from a fibrous product that contains lignin characterized in that the fibrous product is reacted with a binding agent in the presence of an oxidizing chemical or an oxidizing enzyme.
11. A process according to claim 10 wherein the binding agent is a hydrophilic carbohydrate or a protein.
12. A process according to claim 11 wherein the binding agent is cationic starch.
13. A process according to any one of claims 10, 11 and 12 wherein the oxidation is carried out with an oxidizing chemical that forms free radicals.
14. A process according to claim 13 wherein the oxidizing chemical is hydrogen peroxide together with ferrous ions, chlorine dioxide or ozone or a mixture thereof.
15. A process according to any one of claims 10, 11 and 12 wherein the oxidizing enzyme is laccase, lignin peroxidase, manganese peroxidase, hydrogen peroxide or a mixture thereof.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FI895930 | 1989-12-12 | ||
| FI895930A FI85389C (en) | 1989-12-12 | 1989-12-12 | FOERFARANDE FOER TILLVERKNING AV MASSA. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2031972A1 true CA2031972A1 (en) | 1991-06-13 |
Family
ID=8529501
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002031972A Abandoned CA2031972A1 (en) | 1989-12-12 | 1990-12-11 | Procedure for the production of pulp |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0433258A1 (en) |
| JP (1) | JPH03260188A (en) |
| CA (1) | CA2031972A1 (en) |
| FI (1) | FI85389C (en) |
| NO (1) | NO174167C (en) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2082185C (en) * | 1991-11-26 | 2004-01-20 | Alexander R. Pokora | Protease catalyzed treatments of lignocellulose materials |
| DK64092D0 (en) * | 1992-05-18 | 1992-05-18 | Novo Nordisk As | |
| US5480801A (en) * | 1993-09-17 | 1996-01-02 | Novo Nordisk A/S | Purified PH neutral Rhizoctonia laccases and nucleic acids encoding same |
| PT772717E (en) * | 1994-07-26 | 2001-11-30 | Novozymes As | PROCESS FOR PREPARING A PRODUCT BASED ON LIGNOCELLULOSE AND PRODUCT OBTAINED THROUGH THIS PROCESS |
| BR9611393A (en) * | 1995-11-08 | 1999-07-13 | Novo Nordisk As | Lignocellulose-based products and process for the manufacture thereof |
| PT879318E (en) | 1996-02-08 | 2002-07-31 | Novozymes As | A PROCESS FOR INCREASING THE NEGATIVE CHARGE OF A LIGNOCELLULOSIC MATERIAL AND A MODIFIED LIGNOCELLULOSIC MATERIAL WITH AN INCREASED LOAD DENSITY |
| CN1281818C (en) * | 1999-11-19 | 2006-10-25 | 巴科曼实验室国际公司 | Paper making processes using enzyme and polymer compositions |
| US6939437B1 (en) | 1999-11-19 | 2005-09-06 | Buckman Laboratories International, Inc. | Paper making processes using enzyme and polymer combinations |
| EP1264037A2 (en) * | 2000-02-09 | 2002-12-11 | Akzo Nobel N.V. | Pulping process |
| FI20012375A0 (en) * | 2001-12-03 | 2001-12-03 | Dynea Chemicals Oy | Process for making pressed layer structures |
| FI20031904A7 (en) * | 2003-12-23 | 2005-06-24 | Kemira Oyj | Method for modifying a lignocellulosic product |
| US8317975B2 (en) | 2004-04-20 | 2012-11-27 | The Research Foundation Of The State University Of New York | Product and processes from an integrated forest biorefinery |
| CN101171386B (en) | 2005-05-04 | 2011-11-16 | 诺维信北美公司 | Chlorine dioxide treatment compositions and methods |
| DE102008020642A1 (en) * | 2008-04-24 | 2009-10-29 | Kronotec Ag | Process for the production of wood-based materials and wood-based materials |
| WO2021191097A1 (en) | 2020-03-26 | 2021-09-30 | Metgen Oy | Method for making moisture-resistant paper |
| CN117733977A (en) * | 2024-01-11 | 2024-03-22 | 河北犇昂新材料有限公司 | Modifier for efficiently softening and fluffing wood |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ216726A (en) * | 1985-07-15 | 1990-08-28 | Repligen Corp | Use of lignin-degrading enzymes from phanerochaete chrysosporium for treatment of wood pulp and e1 effluent |
| DE3636208A1 (en) * | 1986-10-24 | 1988-05-05 | Call Hans Peter | METHOD FOR DELIGNIFYING AND WHICH BLEACHING LIGNICELLULOSE-CONTAINING OR LIGNINAL MATERIAL OR LIGNIN BY ENZYMATIC TREATMENT |
-
1989
- 1989-12-12 FI FI895930A patent/FI85389C/en active IP Right Grant
-
1990
- 1990-12-11 NO NO905352A patent/NO174167C/en unknown
- 1990-12-11 CA CA002031972A patent/CA2031972A1/en not_active Abandoned
- 1990-12-11 EP EP90850402A patent/EP0433258A1/en not_active Withdrawn
- 1990-12-12 JP JP2415715A patent/JPH03260188A/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| NO905352L (en) | 1991-06-13 |
| NO905352D0 (en) | 1990-12-11 |
| NO174167C (en) | 1994-03-23 |
| FI895930A0 (en) | 1989-12-12 |
| EP0433258A1 (en) | 1991-06-19 |
| NO174167B (en) | 1993-12-13 |
| FI895930L (en) | 1991-06-13 |
| FI85389B (en) | 1991-12-31 |
| FI85389C (en) | 1992-04-10 |
| JPH03260188A (en) | 1991-11-20 |
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