JPH0217678B2 - - Google Patents
Info
- Publication number
- JPH0217678B2 JPH0217678B2 JP63221502A JP22150288A JPH0217678B2 JP H0217678 B2 JPH0217678 B2 JP H0217678B2 JP 63221502 A JP63221502 A JP 63221502A JP 22150288 A JP22150288 A JP 22150288A JP H0217678 B2 JPH0217678 B2 JP H0217678B2
- Authority
- JP
- Japan
- Prior art keywords
- pulp
- bleached
- paper
- treatment
- bleaching
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229920001131 Pulp (paper) Polymers 0.000 claims abstract description 25
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 24
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 12
- 150000002978 peroxides Chemical class 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 239000001569 carbon dioxide Substances 0.000 claims description 8
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 claims description 8
- 239000000725 suspension Substances 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 4
- 238000004140 cleaning Methods 0.000 claims description 3
- 238000012958 reprocessing Methods 0.000 claims description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 abstract description 12
- 238000000034 method Methods 0.000 abstract description 10
- 238000006386 neutralization reaction Methods 0.000 abstract description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 abstract 1
- 238000000746 purification Methods 0.000 abstract 1
- 235000010269 sulphur dioxide Nutrition 0.000 abstract 1
- 239000004291 sulphur dioxide Substances 0.000 abstract 1
- 238000004061 bleaching Methods 0.000 description 15
- 239000000123 paper Substances 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 239000007844 bleaching agent Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- OSVXSBDYLRYLIG-UHFFFAOYSA-N dioxidochlorine(.) Chemical compound O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 239000002655 kraft paper Substances 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 238000010979 pH adjustment Methods 0.000 description 2
- 235000019795 sodium metasilicate Nutrition 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000004155 Chlorine dioxide Substances 0.000 description 1
- BPRJTLAULHNDLP-UHFFFAOYSA-N Chloropanaxydiol Chemical compound CCCCCCCC1OC1CC#CC#CC(O)C(O)CCl BPRJTLAULHNDLP-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 235000019398 chlorine dioxide Nutrition 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 238000004076 pulp bleaching Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000002087 whitening effect Effects 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Paper (AREA)
- Materials For Medical Uses (AREA)
- Diaphragms For Electromechanical Transducers (AREA)
- Ultra Sonic Daignosis Equipment (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、ストレーナー又はペーパーマシーン
を通過させる直前に、H(次亜塩素酸塩)又はP
(過酸化物)により漂白する紙パルプの製造方法
に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention provides a method for removing H (hypochlorite) or P immediately before passing through a strainer or paper machine.
The present invention relates to a method for producing paper pulp by bleaching with (peroxide).
紙パルプ産業において、そのタイプが何であつ
ても、即ち機械パルプ、化学パルプ、又は脱イン
ク紙の再処理により得たパルプであつても、パル
プの漂白はパルプからの紙の製造前に行われる。 In the pulp and paper industry, pulp bleaching is carried out before the production of paper from pulp, whatever its type, i.e. mechanical pulp, chemical pulp, or pulp obtained by reprocessing deinked paper. .
漂白工程は、一般に洗浄工程によつて分離され
ている1つ又はそれ以上の連続ステージから構成
される。これらのステージは、使用される漂白剤
により特徴づけられる。例えば、化学パルプ特に
クラフトの場合には、CEHH、CEP、CEDED、
CEDP、CEHDP、およびCEDED(P)及び
CEHD(P)、亜硫酸パルプの場合には、CEH、
HH、H及びOH、機械パルプの場合には、RP、
PP、RPRP、PRP又はP、セミケミカルパルプ
の場合には、P、HH、OHの一連のステージ列
が用いられ。 Bleaching processes generally consist of one or more successive stages separated by washing steps. These stages are characterized by the bleaching agent used. For example, for chemical pulp especially kraft, CEHH, CEP, CEDED,
CEDP, CEHDP, and CEDED(P) and
CEHD(P), CEH for sulphite pulp,
HH, H and OH, RP for mechanical pulp,
For PP, RPRP, PRP or P, semi-chemical pulps, a series of stages P, HH, OH is used.
漂白プロセスを実施している公知刊行物とし
て、例えば米国特許第3806404号、殴州特許第
187477号がある。 Publications implementing the bleaching process include, for example, U.S. Pat. No. 3,806,404;
There is number 187477.
漂白工程の最後には、通常、SO2によるパルプ
の処理が行われ、それはパルプのストレイニング
および/又はペーパーマシーンへの通過前に行わ
れる。一般に溶液中での二酸化硫黄による処理
は、次のような目的及び効果を有する。即ち、そ
れらがD処理(二酸化塩素)、H処理(次亜塩素
酸塩)、又はP処理(過酸化物)の残渣であると
にかかわらず、漂白ステージの残渣又は化学的残
渣を破壊すること、白さを減少させ、白さの逆の
プロセスを促進する金属カチオン(鉄、マンガン
又は銅)を除去ること、アルカリ性はパルプ及び
紙を黒くする有害な効果を有するので、パルプを
酸性化すること、である。従つて、この最後の点
が基本的である。 The end of the bleaching process is usually a treatment of the pulp with SO 2 before it is strained and/or passed to a paper machine. Generally, treatment with sulfur dioxide in a solution has the following objectives and effects. i.e., destroying the residues or chemical residues of the bleaching stage, whether they are residues of the D treatment (chlorine dioxide), the H treatment (hypochlorite), or the P treatment (peroxide). , removing metal cations (iron, manganese or copper) which reduce whiteness and promote the opposite process of whitening, acidifying the pulp as alkalinity has the detrimental effect of blackening the pulp and paper. That is. This last point is therefore fundamental.
この多くの“SO2効果”は、“加酸漂白
(souring)”として知られている。 This many " SO2 effects" are known as "souring."
ClO2は腐蝕性であり、毒性があり、その存在
は処理の残りと両立しない(洗浄機の腐蝕)の
で、残渣の破壊はD処理(ClO2)の場合に必要
である。 Destruction of the residue is necessary in the case of D treatment (ClO 2 ), since ClO 2 is corrosive and toxic and its presence is incompatible with the rest of the treatment (washer corrosion).
しかし、一方、H又はP処理の場合には、残渣
は有害ではないことが見出だされた。それらは漂
白剤として作用し続け、かつ穏やかな殺生物作用
を有するので、それらの存在は好ましい効果を有
する。 However, on the other hand, it has been found that in case of H or P treatment, the residue is not harmful. Their presence has a favorable effect, since they continue to act as bleaching agents and have a mild biocidal effect.
本発明者は、最終のH又はPステージ又は単一
のH又はPステージを採用する漂白処理の場合
に、SO2の使用は必要ではなく、パルプはSO2に
よつてではなくCO2によつて中和することが出来
ることを見出だした。 The inventors have discovered that in the case of bleaching processes employing a final H or P stage or a single H or P stage, the use of SO 2 is not necessary and the pulp is depleted by CO 2 rather than by SO 2 . We have discovered that it is possible to neutralize the
従つて、本発明によると、漂白されたパルプを
ストレーナー及び/又はペーパーマシーンを通過
させる直前に、次亜塩素酸塩又は過酸化物により
漂白する紙パルプの製造方法であつて、前記漂白
されたパルプは漂白処理の直後に基本的に二酸化
炭素により処理されることを特徴とする紙パルプ
の製造方法が提供される。 Therefore, according to the present invention, there is provided a method for producing paper pulp, which comprises bleaching the bleached pulp with hypochlorite or peroxide immediately before passing it through a strainer and/or a paper machine, comprising: A method for producing paper pulp is provided, characterized in that the pulp is treated with carbon dioxide essentially immediately after the bleaching treatment.
本発明のプロセスは、最後の又は単一のステー
ジがH又はPタイプであれば、パルプが機械パル
プ又は化学パルプ又は脱インク紙の再生により得
たパルプのいずれであつても、及び漂白工程のど
こにおいても、多段タイプ又は単一タイプのいず
れであつても用いることが出来る。 The process of the present invention is suitable for the bleaching step, whether the pulp is mechanical pulp or chemical pulp or pulp obtained by recycling deinked paper, provided that the last or single stage is H or P type. Either multistage or single type can be used everywhere.
このように、本発明は、通常漂白処理のみを行
なう熱機械パルプ(TMP)又は化学―熱機械パ
ルプ(CTMP)に適用される。 Thus, the invention applies to thermomechanical pulps (TMP) or chemical-thermomechanical pulps (CTMP), which are normally subjected to only bleaching treatment.
このH又はPステージの後に、パルプは通常洗
浄され、懸濁液の形で処理される。 After this H or P stage, the pulp is usually washed and processed in suspension form.
本発明に従い、二酸化炭素が最後の又は単一の
ステージの洗浄液に導入される。それはまた、最
後の又は単一の漂白ステージからの発生の際に懸
濁液に導入さてもよい。 According to the invention, carbon dioxide is introduced into the last or single stage cleaning fluid. It may also be introduced into the suspension during development from the last or single bleaching stage.
二酸化炭素は、ガス状又は液状又は溶液中に溶
解した形で、例えば懸濁液の洗浄又は稀釈水に導
入することが出来る。 Carbon dioxide can be introduced in gaseous or liquid form or dissolved in solution, for example in the suspension wash or dilution water.
本発明による中和処理の後、パルプは通常の手
順で処理される。即ち、例えば貯蔵され、又は直
接ペーパーマシーンに導入され、又は精製され
る。 After the neutralization treatment according to the invention, the pulp is processed in the usual manner. That is, for example, it can be stored or introduced directly into a paper machine or purified.
パルプを中和する目的を満足するという事実に
加え、本発明による二酸化炭素の使用は、有害な
アルカリ条件を避け、(実施例により明かなよう
に)SO2によるよりも優れている満足すべき漂白
結果を与え、かつ次の利点を有する。 In addition to the fact that it satisfies the purpose of neutralizing the pulp, the use of carbon dioxide according to the invention avoids harmful alkaline conditions and (as evidenced by the examples) satisfactorily outperforms that with SO2 . gives bleaching results and has the following advantages:
―酸性化は制御が簡単であり、CO2は弱酸であ
り、CO2によるよりも危険が少ない。- Acidification is easy to control and CO2 is a weak acid, making it less dangerous than with CO2 .
―酸の使用による腐蝕及び洗浄液の汚染は存在し
ない。- There is no corrosion and contamination of cleaning fluids due to the use of acids.
―P又はHステージの残渣は破壊されず、穏やか
な殺生物性を示すので、例えば貯蔵の際に生
じ、パルプを黒くする微生物の生育が避けられ
る。- The P or H stage residues are not destroyed and have mild biocidal properties, thus avoiding the growth of microorganisms which occur, for example, during storage and which darken the pulp.
―注入操作は簡単である。-The injection operation is easy.
―破壊されない漂白処理残渣を再使用することが
出来る。- Indestructible bleaching residue can be reused.
本発明の他の特徴及び利点は、以下の実施例に
より明かであろう。なお、以下の実施例は、パル
プのPH及び白色度を調節するための二酸化炭素の
種々の非制限的使用を示している。 Other features and advantages of the invention will become apparent from the following examples. It should be noted that the following examples demonstrate various non-limiting uses of carbon dioxide to adjust the PH and brightness of pulp.
実施例 1
熱機械パルプがPRP漂白工程で処理された。
第2のP処理の後、70.65%ISOの白色度が得ら
れた。第2のP処理は、パルプ重量に基づき、2
%H2O2、1.5%NaOH、1.0%Na2SiO3、および
0.05%MgSO4を含む溶液でパルプを処理するこ
とからなる。この場合、パルプ濃度は10%、温度
は65%、保持時間は2時間であつた。Example 1 Thermomechanical pulp was treated with a PRP bleaching process.
After the second P treatment, a whiteness of 70.65% ISO was obtained. The second P treatment is based on pulp weight,
% H2O2 , 1.5%NaOH, 1.0% Na2SiO3 , and
It consists of treating the pulp with a solution containing 0.05% MgSO4 . In this case, the pulp concentration was 10%, the temperature was 65%, and the holding time was 2 hours.
最終PHは8.3であり、残留する過酸化物は、乾
燥パルプの1.3%であつた。 The final PH was 8.3 and the residual peroxide was 1.3% of the dry pulp.
パルプは濃度27%とされ、次の二つのサンプル
に分割された。 The pulp had a consistency of 27% and was divided into two samples:
1 第1のサンプルにはSO2液が加えられ、PH
5.5、濃度10%とされた。1 SO2 solution was added to the first sample, and the pH
5.5, the concentration was set at 10%.
パルプ中に残留過酸化物は無かつた。このサ
ンプルにより製造されたものは80.05%ISOの
白色度を有していた。 There was no residual peroxide in the pulp. This sample produced had a whiteness of 80.05% ISO.
2 濃度10%の懸濁液が得られ、PHを5.7に調節
するように、第2のサンプル及び水にCO2が溶
解された。2 CO 2 was dissolved in the second sample and water to obtain a 10% concentration suspension and adjust the PH to 5.7.
残留過酸化物は変化しなかつた。白色度が決
定され、81.17%ISOであつた。 Residual peroxide remained unchanged. The brightness was determined and was 81.17% ISO.
この実施例により、過酸化物処理後のCO2によ
るPHの調整は、SO2によるPHの調整に比べ、改善
されていることがわかる。 This example shows that PH adjustment using CO 2 after peroxide treatment is improved compared to PH adjustment using SO 2 .
実施例 2
無漂白の熱機械パルプ(白度:57.43%ISO)
を、2%H2O2、2.0%NaOH、2.0%Na2SiO3、お
よび0.05%MgSO4、および0.2%DTPA(ナトリウ
ムジエチレントリミンペンタアセテート)含む溶
液でパルプを処理した。Example 2 Unbleached thermomechanical pulp (whiteness: 57.43% ISO)
The pulp was treated with a solution containing 2% H2O2 , 2.0% NaOH, 2.0 % Na2SiO3 , and 0.05% MgSO4 , and 0.2% DTPA (sodium diethylenetrimine pentaacetate).
この場合、パルプ濃度は10%、温度は85%、保
持時間は30分であつた。 In this case, the pulp concentration was 10%, the temperature was 85%, and the holding time was 30 minutes.
最終PHは8.1であり、残留する過酸化物は、乾
燥パルプの0.61%であつた。 The final PH was 8.1 and the residual peroxide was 0.61% of the dry pulp.
濃度10%の漂白パルプは、次の二つのサンプル
に分割された。 The bleached pulp with a concentration of 10% was divided into two samples:
1 第1のサンプルにはSO2液が加えられ、PH
5.4とされた。1. SO2 solution was added to the first sample, and the pH
It was set as 5.4.
SO2の注入後には残留過酸化物は無かつた。
パルプは排出され、このサンプルにより製造さ
れたものは72.14%ISOの白色度を有していた。 There was no residual peroxide after the SO 2 injection.
The pulp was discharged and produced by this sample had a brightness of 72.14% ISO.
2 PHを5.6となるまで、第2のサンプルにCO2
が注入された。2 Add CO 2 to the second sample until the pH is 5.6.
was injected.
残留過酸化物は0.58%であつた。白色度が決
定され、74.24%ISOであつた。 Residual peroxide was 0.58%. The brightness was determined and was 74.24% ISO.
残留過酸化物は懸濁液から抽出され、更に漂
白されるため回収された。 Residual peroxide was extracted from the suspension and collected for further bleaching.
CO2によるPHの調整後の白色度は、SO2によ
るPHの調整後の白色度に比べ、改善されてい
た。 The whiteness after adjusting the PH with CO 2 was improved compared to the whiteness after adjusting the PH with SO 2 .
実施例 3
樹脂のベースを有する化学クラフトパルプが
CDEODP工程で漂白された。Example 3 Chemical kraft pulp with resin base
Bleached with CDEODP process.
ステージPの後、PHは9.9であり、パルプは、
次の二つのサンプルに分割された。 After stage P, the PH is 9.9 and the pulp is
It was divided into two samples:
1 第1のサンプルはSO2により処理されPH6.0
とされた。懸濁液が排出され、製造されたもの
は86.50%ISOの白色度を有していた。105℃で
の1時間のエージングの後、白色度は83.24%
ISOであつた。1 The first sample was treated with SO 2 and the pH was 6.0.
It was said that The suspension was discharged and the product produced had a whiteness of 86.50% ISO. After 1 hour aging at 105℃, whiteness is 83.24%
It was ISO.
2 PHが6.3に調節されるまで、第2のサンプル
がCO2により処理された。2 A second sample was treated with CO2 until the PH was adjusted to 6.3.
排出後、製造されたものは87.16%ISOの白
色度を有していた。 After discharge, the produced had a whiteness of 87.16% ISO.
105℃での1時間のエージングの後、白色度
は83.24%ISOであつた。 After aging at 105° C. for 1 hour, the whiteness was 83.24% ISO.
この実施例により、CO2によるPHの調整は、
SO2によるPHの調整に比べ、より優れた白色度を
有することがわかる。更に、白色度の逆転は、
CO2を用いた場合よりも少なかつた。 According to this example, the adjustment of PH by CO2 is
It can be seen that the whiteness is superior to that obtained by adjusting the pH using SO 2 . Furthermore, the reversal of whiteness is
It was less than when CO 2 was used.
Claims (1)
ペーパーマシーンを通過させる直前に、次亜塩素
酸塩又は過酸化物により漂白する紙パルプの製造
方法において、前記漂白されたパルプは漂白処理
の直後に基本的に二酸化炭素により処理されるこ
とを特徴とする紙パルプの製造方法。 2 前記二酸化炭素は、ガス状又は液状の形で洗
浄液中に導入される請求項1に記載の紙パルプの
製造方法。 3 前記二酸化炭素は、ガス状又は液状の形で漂
白された懸濁液中に導入される請求項1に記載の
紙パルプの製造方法。 4 前記漂白されたパルプは、機械パルプ、熱機
械パルプ、化学−熱機械パルプ、化学パルプ、又
は脱インク紙の再処理により得たパルプである請
求項1〜3のうちのいずれか1項に記載の紙パル
プの製造方法。[Claims] 1. A method for producing paper pulp in which the bleached pulp is bleached with hypochlorite or peroxide immediately before passing through a strainer and/or a paper machine, wherein the bleached pulp is bleached. A method for producing paper pulp, characterized in that it is essentially treated with carbon dioxide immediately after the treatment. 2. The method for producing paper pulp according to claim 1, wherein the carbon dioxide is introduced into the cleaning liquid in a gaseous or liquid form. 3. A method for producing paper pulp according to claim 1, wherein the carbon dioxide is introduced into the bleached suspension in gaseous or liquid form. 4. The bleached pulp is mechanical pulp, thermomechanical pulp, chemical-thermomechanical pulp, chemical pulp, or pulp obtained by reprocessing deinked paper. The method for producing the paper pulp described.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8712451 | 1987-09-08 | ||
FR8712451A FR2620144B1 (en) | 1987-09-08 | 1987-09-08 | PROCESS FOR THE MANUFACTURE OF BLEACHED PAPER PULP INCLUDING TREATMENT WITH CARBONIC ACID AFTER BLEACHING |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01207492A JPH01207492A (en) | 1989-08-21 |
JPH0217678B2 true JPH0217678B2 (en) | 1990-04-23 |
Family
ID=9354710
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63221502A Granted JPH01207492A (en) | 1987-09-08 | 1988-09-06 | Production of paper pulp |
Country Status (18)
Country | Link |
---|---|
EP (1) | EP0307295B1 (en) |
JP (1) | JPH01207492A (en) |
KR (1) | KR890005346A (en) |
CN (1) | CN1013131B (en) |
AT (1) | ATE62287T1 (en) |
AU (1) | AU608054B2 (en) |
BR (1) | BR8804619A (en) |
DE (1) | DE3862265D1 (en) |
ES (1) | ES2021857B3 (en) |
FI (1) | FI884123A (en) |
FR (1) | FR2620144B1 (en) |
GR (1) | GR3001730T3 (en) |
MA (1) | MA21393A1 (en) |
NO (1) | NO883968L (en) |
NZ (1) | NZ226060A (en) |
OA (1) | OA08949A (en) |
PT (1) | PT88435B (en) |
ZA (1) | ZA886622B (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9206415D0 (en) * | 1992-03-24 | 1992-05-06 | Albright & Wilson | Stabilisation of bleach liquors |
US5639347A (en) * | 1993-03-24 | 1997-06-17 | Ahlstrom Machinery Inc. | Method of controlling of metals in a bleach plant, using oxidation |
US5509999A (en) * | 1993-03-24 | 1996-04-23 | Kamyr, Inc. | Treatment of bleach plant effluents |
FI110533B (en) * | 2000-05-04 | 2003-02-14 | Aga Ab | Method for controlling microbial growth |
WO2011113119A1 (en) * | 2010-03-19 | 2011-09-22 | Fibria Celulose S/A | Process for the treatment of cellulose pulps, cellulose pulp thus obtained and use of biopolymer for treating cellulose pulps |
CN104032611B (en) * | 2014-06-23 | 2016-04-20 | 广西大学 | A kind of dioxde pulp bleaching process |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1993265A (en) * | 1933-02-28 | 1935-03-05 | Merrimac Chemical Co Inc | Manufacture of paper embodying alkaline earth metal carbonate fillers |
FI52876C (en) * | 1974-09-03 | 1978-10-17 | Ahlstroem Oy | OVERFLOWER FOR CELLULOSE FRAON ALKALIKOK |
-
1987
- 1987-09-08 FR FR8712451A patent/FR2620144B1/en not_active Expired
-
1988
- 1988-09-05 DE DE8888402223T patent/DE3862265D1/en not_active Expired - Fee Related
- 1988-09-05 AT AT88402223T patent/ATE62287T1/en active
- 1988-09-05 EP EP88402223A patent/EP0307295B1/en not_active Expired - Lifetime
- 1988-09-05 ES ES88402223T patent/ES2021857B3/en not_active Expired - Lifetime
- 1988-09-06 JP JP63221502A patent/JPH01207492A/en active Granted
- 1988-09-06 ZA ZA886622A patent/ZA886622B/en unknown
- 1988-09-06 PT PT88435A patent/PT88435B/en not_active IP Right Cessation
- 1988-09-06 NZ NZ226060A patent/NZ226060A/en unknown
- 1988-09-07 KR KR1019880011536A patent/KR890005346A/en not_active Application Discontinuation
- 1988-09-07 NO NO88883968A patent/NO883968L/en unknown
- 1988-09-07 MA MA21615A patent/MA21393A1/en unknown
- 1988-09-07 AU AU21960/88A patent/AU608054B2/en not_active Ceased
- 1988-09-07 FI FI884123A patent/FI884123A/en not_active IP Right Cessation
- 1988-09-08 CN CN88106618A patent/CN1013131B/en not_active Expired
- 1988-09-08 BR BR8804619A patent/BR8804619A/en unknown
- 1988-09-08 OA OA59425A patent/OA08949A/en unknown
-
1991
- 1991-04-04 GR GR90401231T patent/GR3001730T3/en unknown
Also Published As
Publication number | Publication date |
---|---|
ZA886622B (en) | 1991-05-29 |
NO883968D0 (en) | 1988-09-07 |
BR8804619A (en) | 1989-04-18 |
AU2196088A (en) | 1989-03-09 |
FI884123A0 (en) | 1988-09-07 |
FI884123A (en) | 1989-03-09 |
NZ226060A (en) | 1991-02-26 |
DE3862265D1 (en) | 1991-05-08 |
EP0307295A1 (en) | 1989-03-15 |
NO883968L (en) | 1989-03-09 |
MA21393A1 (en) | 1989-07-01 |
KR890005346A (en) | 1989-05-13 |
ES2021857B3 (en) | 1991-11-16 |
OA08949A (en) | 1990-11-30 |
ATE62287T1 (en) | 1991-04-15 |
CN1013131B (en) | 1991-07-10 |
GR3001730T3 (en) | 1992-11-23 |
PT88435B (en) | 1992-10-30 |
EP0307295B1 (en) | 1991-04-03 |
FR2620144B1 (en) | 1989-12-08 |
JPH01207492A (en) | 1989-08-21 |
PT88435A (en) | 1989-07-31 |
FR2620144A1 (en) | 1989-03-10 |
CN1033664A (en) | 1989-07-05 |
AU608054B2 (en) | 1991-03-21 |
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