JPH09503028A - Chlorine-free bleaching of chemical pulp including two-step treatment with chelating agents - Google Patents

Chlorine-free bleaching of chemical pulp including two-step treatment with chelating agents

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Publication number
JPH09503028A
JPH09503028A JP7509711A JP50971195A JPH09503028A JP H09503028 A JPH09503028 A JP H09503028A JP 7509711 A JP7509711 A JP 7509711A JP 50971195 A JP50971195 A JP 50971195A JP H09503028 A JPH09503028 A JP H09503028A
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JP
Japan
Prior art keywords
pulp
bleaching
ozone
peroxide
chlorine
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.)
Pending
Application number
JP7509711A
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Japanese (ja)
Inventor
ダール,モルテン
ノルデーン,シヨルベイゲ
Original Assignee
シユンドス・デフイブラトール・インダストリーズ・アクテイエボラーグ
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Application filed by シユンドス・デフイブラトール・インダストリーズ・アクテイエボラーグ filed Critical シユンドス・デフイブラトール・インダストリーズ・アクテイエボラーグ
Publication of JPH09503028A publication Critical patent/JPH09503028A/en
Pending legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21CPRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C9/00After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
    • D21C9/10Bleaching ; Apparatus therefor
    • D21C9/1026Other features in bleaching processes
    • D21C9/1042Use of chelating agents
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21CPRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C9/00After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
    • D21C9/10Bleaching ; Apparatus therefor
    • D21C9/147Bleaching ; Apparatus therefor with oxygen or its allotropic modifications
    • D21C9/153Bleaching ; Apparatus therefor with oxygen or its allotropic modifications with ozone
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21CPRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C9/00After-treatment of cellulose pulp, e.g. of wood pulp, or cotton linters ; Treatment of dilute or dewatered pulp or process improvement taking place after obtaining the raw cellulosic material and not provided for elsewhere
    • D21C9/10Bleaching ; Apparatus therefor
    • D21C9/16Bleaching ; Apparatus therefor with per compounds
    • D21C9/163Bleaching ; Apparatus therefor with per compounds with peroxides

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  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Paper (AREA)

Abstract

(57)【要約】 パルプをキレート化剤で処理し、オゾン及び過酸化物で漂白する、化学パルプ形態のリグノセルロース含有繊維材料の塩素漂白剤を用いない漂白法であって、オゾン漂白した直後に、第2段階キレート化段階で、1〜10%のパルプ濃度で、1〜30分間、20〜90℃の温度及び1.5〜5のpH値でパルプをキレート化剤で処理し、このようにして処理したパルプを過酸化物漂白する前に8〜40%の濃度まで洗浄、脱水する。 (57) [Summary] A chlorine bleach-free bleaching method of lignocellulose-containing fiber material in the form of chemical pulp, which comprises bleaching pulp with a chelating agent and bleaching with ozone and peroxide, immediately after ozone bleaching. In the second stage chelation stage, the pulp is treated with a chelating agent at a pulp concentration of 1-10% for 1-30 minutes at a temperature of 20-90 ° C. and a pH value of 1.5-5. The pulp thus treated is washed and dewatered to a concentration of 8-40% before peroxide bleaching.

Description

【発明の詳細な説明】 キレート化剤で2段階処理することを含む化学パルプの無塩素漂白 本発明は、化学パルプ形態のリグノセルロース含有材料の塩素漂白剤を用いな い漂白に関する。より特定的には、本発明は、パルプをオゾン漂白し、次いで過 酸化物漂白することに関する。 パルプのオゾン漂白をより選択的に行うために、先ず、パルプを、キレート化 剤、例えば、DTPA又はEDTAで処理する。それによって、金属イオンがパ ルプから溶解し、オゾン漂白の前に脱水して該イオンを除去する。 オゾン漂白したパルプは、一部が繊維に吸収され、一部が周囲の液体に溶解し た金属を依然として含んでいる。これらの金属は、次の段階で過酸化物漂白し得 るように除去しなければならない。 慣用法によれば、キレート化剤による処理は、1〜10%のパルプ濃度で、1 〜60分間、20〜70℃の温度、2〜5のpH値で行う。その後で、パルプを 脱水し、オゾンで漂白する。オゾン漂白の後、パルプを洗浄、脱水し、その後、 過酸化物漂白を行う。あるいは、洗浄、脱水した 後でキレート化剤による追加処理を行う。このキレート化剤による処理は、通常 、60〜90℃で30〜120分間行う。その後で、過酸化物漂白の前に、パル プを再び洗浄、脱水する。 上記公知法の最初のものでは満足すべきISO白色度は得られず、別の方法は 、プロセスを複雑化し、より高価にする追加段階を必要とする。 方法が比較的簡易であり且つパルプの高ISO白色度が得られる本発明により 、これらの問題が排除される。 本発明の特徴は、添付請求の範囲から明らかである。 本発明を添付図面を参照して以下に詳細に説明する。 図1は、本発明の方法の流れ図である。 図2は、それぞれ公知方法及び本発明方法の場合の過酸化物充填量の関数とし ての白色度を示す図である。 図1の流れ図によれば、先ず、化学パルプをEDTA又はDTPAで処理する ために、第1のキレート化段階10に供給する。パルプ濃度は1〜10%でなけ ればならず、処理は、1〜60分間、好ましくは5〜30分間行う。温度は、2 0〜70℃、好ましくは20〜40℃、pH値は2〜5でなければならない。 第1キレート化段階10の後、溶解した金属イオンを除去するために、パルプ を洗浄し、例えば洗浄プレス11中で脱水する。パルプを該プレスからオゾン漂 白用のオゾン段階12に送る。オゾン段階12の直後に、パルプを1〜10%濃 度に希釈し、第2キレート化段階13に供給する。該段階で、1〜30分間、好 ましくは5〜20分間、20〜90℃、好ましくは40〜80℃の温度、1.5 〜5のpH値でパルプをキレート化剤、好ましくはDTPA又はEDTAで処理 する。充填するDTPA又はEDTAの量は、パルプ1トン当たり0.5kgま でが好ましい。 この第2キレート化段階13の後、第2洗浄段階14で、8〜40%の濃度に なるまで洗浄及び脱水を行い、その後、パルプを過酸化物漂白用の過酸化物段階 15に送る。 この方法により、パルプは83%ISOを超える白色度まで漂白し得る。 図2に、オゾンと過酸化物段階の間の種々の処理で充填された過酸化物の関数 としての白色度が示されている。 曲線1は、オゾン漂白したパルプを1回洗浄、脱水した後、過酸化物漂白する 慣用法に関する。 曲線2は、公知方法で洗浄、脱水、キレート化剤で処理 し、過酸化物漂白の前に再び洗浄、脱水した、オゾン漂白したパルプの過酸化物 漂白に関する。 曲線3は、本発明による方法に関する。 図2から、本発明の漂白(曲線3)により、曲線1の慣用漂白より著しく良好 な結果が得られることが明らかである。さらに、本発明の漂白法は、極めて簡易 であるにも拘わらず、実質的に曲線3の漂白結果に相当する結果が得られること も明らかである。ミル環境で実施された実験でも、最後の2種の方法(曲線2及 び3)の差は非常に小さいものであることが証明されている。 本発明が、示されている実施態様には限定されず、本発明の概念の範囲内であ れば変更が可能であることは勿論である。Detailed Description of the Invention Chlorine-free bleaching of chemical pulp including two-step treatment with chelating agents   The present invention does not use chlorine bleach for lignocellulose-containing materials in the form of chemical pulp. About bleaching. More specifically, the present invention ozone bleaches pulp and then Regarding oxide bleaching.   In order to make ozone bleaching of pulp more selective, first, pulp is chelated. Treat with an agent such as DTPA or EDTA. As a result, metal ions are Dissolve from the loop and dehydrate to remove the ions prior to ozone bleaching.   Ozone bleached pulp is partially absorbed by the fibers and partially dissolved in the surrounding liquid. Still contains metal. These metals can be peroxide bleached in the next step Must be removed.   According to conventional practice, treatment with a chelating agent at a pulp concentration of 1-10% -60 minutes at a temperature of 20-70 ° C and a pH value of 2-5. After that, the pulp Dehydrate and bleach with ozone. After ozone bleaching, the pulp is washed and dehydrated, then Perform peroxide bleaching. Alternatively, washed and dehydrated Later, additional treatment with a chelating agent is performed. Treatment with this chelating agent is usually , 60 to 90 ° C. for 30 to 120 minutes. Then, before the peroxide bleaching, Wash and dehydrate the pump again.   The first of the above known methods does not give a satisfactory ISO whiteness, the other method is , Requires additional steps that complicate the process and make it more expensive.   According to the present invention, the method is relatively simple and the high ISO whiteness of pulp is obtained. , These problems are eliminated.   Features of the invention will be apparent from the appended claims.   The present invention will be described in detail below with reference to the accompanying drawings.   FIG. 1 is a flow chart of the method of the present invention.   FIG. 2 is a function of peroxide loading for the known method and the method of the present invention, respectively. It is a figure which shows the whiteness of all.   According to the flow chart of FIG. 1, first the chemical pulp is treated with EDTA or DTPA. In order to do so, feed to the first chelation stage 10. Pulp concentration should be 1-10% No treatment is necessary, and the treatment is carried out for 1 to 60 minutes, preferably 5 to 30 minutes. The temperature is 2 It should be between 0 and 70 ° C, preferably between 20 and 40 ° C and the pH value should be between 2 and 5.   After the first chelation step 10, pulp is removed to remove dissolved metal ions. Are washed and dehydrated, for example in a washing press 11. Pulp from the press is ozone-dried. Send to the ozone stage 12 for white. Immediately after the ozone stage 12, the pulp is concentrated by 1-10%. Dilute once and feed to the second chelation stage 13. At this stage, 1 to 30 minutes The temperature is preferably 20 to 90 ° C, preferably 40 to 80 ° C for 5 to 20 minutes, 1.5 Treat pulp with a chelating agent, preferably DTPA or EDTA, at a pH value of ~ 5 I do. The amount of DTPA or EDTA to be filled is 0.5 kg per ton of pulp. Is preferred.   After this second chelation step 13, in a second washing step 14, a concentration of 8-40% is obtained. Washed and dehydrated until complete, and then the pulp is treated with a peroxide stage for peroxide bleaching. Send to 15.   By this method the pulp can be bleached to a whiteness above 83% ISO.   Figure 2 shows the function of peroxide loaded with various treatments between ozone and peroxide stages. As whiteness is shown.   Curve 1 is ozone bleached pulp washed once, dehydrated and then peroxide bleached Regarding idiomatic usage.   Curve 2 is washed, dehydrated and treated with chelating agents by known methods Ozone bleached pulp peroxide, which had been washed and dehydrated again prior to peroxide bleaching Regarding bleaching.   Curve 3 relates to the method according to the invention.   From FIG. 2 it is seen that the bleaching of the invention (curve 3) is significantly better than the conventional bleaching of curve 1. It is clear that various results are obtained. Furthermore, the bleaching method of the present invention is extremely simple. That the result is substantially equivalent to the bleaching result of curve 3 Is also clear. In the experiment conducted in the mill environment, the last two methods (curve 2 and It has been proved that the difference between 3 and 3) is very small.   The invention is not limited to the embodiments shown, which are within the scope of the inventive concept. Of course, it can be changed.

Claims (1)

【特許請求の範囲】 1.パルプをキレート化剤で処理し、オゾン及び過酸化物で漂白する、化学パル プ形態のリグノセルロース含有繊維材料の塩素漂白剤を用いない漂白法であって 、オゾン漂白した直後に、第2段階キレート化段階で、1〜10%のパルプ濃度 で、1〜30分間、20〜90℃の温度及び1.5〜5のpH値でパルプをキレ ート化剤で処理し、このようにして処理したパルプを過酸化物漂白する前に8〜 40%の濃度まで洗浄、脱水することを特徴とする方法。 2.第2キレート化段階のキレート化剤として、DTPA又はEDTAを用い、 該キレート化剤をパルプ1トン当たり0.5kgまでの量で添加することを特徴 とする請求項1に記載の方法。 3.漂白を83%ISOを超える白色度まで実施することを特徴とする請求項1 又は2に記載の方法。[Claims] 1. Chemical pulp treated with pulp chelating agent and bleaching with ozone and peroxide A bleaching method for chlorine-free bleaching of lignocellulosic fiber materials in the form of Immediately after ozone bleaching, in the second stage chelation stage, 1-10% pulp concentration At a temperature of 20 to 90 ° C. and a pH value of 1.5 to 5 for 1 to 30 minutes. The pulp treated with a oxidising agent and treated in this way is A method comprising washing and dehydrating to a concentration of 40%. 2. Using DTPA or EDTA as the chelating agent in the second chelation step, Characterized in that the chelating agent is added in an amount of up to 0.5 kg per ton of pulp The method according to claim 1, wherein 3. Bleaching is performed to a whiteness of more than 83% ISO. Or the method of 2.
JP7509711A 1993-09-21 1994-08-22 Chlorine-free bleaching of chemical pulp including two-step treatment with chelating agents Pending JPH09503028A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
SE9303066A SE501836C2 (en) 1993-09-21 1993-09-21 Bleaching of chemical pulp whereby the pulp is treated with complexing agents before and after an ozone step
SE9303066-6 1993-09-21
PCT/SE1994/000758 WO1995008666A1 (en) 1993-09-21 1994-08-22 Chlorine-free bleaching of chemical pulp involving a two stage treatment with chelating agent

Publications (1)

Publication Number Publication Date
JPH09503028A true JPH09503028A (en) 1997-03-25

Family

ID=20391160

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7509711A Pending JPH09503028A (en) 1993-09-21 1994-08-22 Chlorine-free bleaching of chemical pulp including two-step treatment with chelating agents

Country Status (9)

Country Link
EP (1) EP0720675A1 (en)
JP (1) JPH09503028A (en)
AU (1) AU7792394A (en)
BR (1) BR9407555A (en)
CA (1) CA2168445A1 (en)
FI (1) FI961279A (en)
NO (1) NO961139L (en)
SE (1) SE501836C2 (en)
WO (1) WO1995008666A1 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE504803C2 (en) * 1995-08-24 1997-04-28 Sunds Defibrator Ind Ab Treatment of pulp with complexing agents in at least two mixing steps without intermediate washing
SE508239C2 (en) * 1997-01-03 1998-09-21 Sunds Defibrator Ind Ab Treatment of pulp with complexing agents in at least one mixing step, without the use of the bleaching tower
CN102587186B (en) * 2012-03-20 2015-03-11 昆明理工大学 Method for bleaching dendrocalamus giganteus chemical pulp
RU2634586C1 (en) * 2016-08-01 2017-10-31 федеральное государственное бюджетное образовательное учреждение высшего образования "Пермский национальный исследовательский политехнический университет" Method of bleaching hardwood sulphate cellulose

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR9205490A (en) * 1991-01-03 1994-04-05 Union Camp Patent Holding Processes for the manufacture of bleached pulp having a final GE britho of at least about 75 and for the delignification and bleaching of a lignocellulosic pulp
SE468355B (en) * 1991-04-30 1992-12-21 Eka Nobel Ab CHEMISTRY OF CHEMICAL MASS THROUGH TREATMENT WITH COMPLEX PICTURES AND OZONE

Also Published As

Publication number Publication date
SE9303066D0 (en) 1993-09-21
AU7792394A (en) 1995-04-10
EP0720675A1 (en) 1996-07-10
BR9407555A (en) 1996-12-31
FI961279A0 (en) 1996-03-20
WO1995008666A1 (en) 1995-03-30
SE9303066L (en) 1995-03-22
NO961139D0 (en) 1996-03-20
SE501836C2 (en) 1995-05-22
FI961279A (en) 1996-03-20
NO961139L (en) 1996-03-20
CA2168445A1 (en) 1995-03-30

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