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JPS6354836B2 - - Google Patents
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JPS6354836B2 - - Google Patents

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Publication number
JPS6354836B2
JPS6354836B2 JP58160873A JP16087383A JPS6354836B2 JP S6354836 B2 JPS6354836 B2 JP S6354836B2 JP 58160873 A JP58160873 A JP 58160873A JP 16087383 A JP16087383 A JP 16087383A JP S6354836 B2 JPS6354836 B2 JP S6354836B2
Authority
JP
Japan
Prior art keywords
pulp
coarse
wood fiber
fiber raw
pretreatment
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
Application number
JP58160873A
Other languages
Japanese (ja)
Other versions
JPS6052691A (en
Inventor
Yoshio Kobayashi
Ryukichi Matsuo
Masashi Nishama
Satoru Nojima
Kunio Umeda
Takashi Sato
Mutsuo Yoshinaga
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
National Institute of Advanced Industrial Science and Technology AIST
Shingijutsu Kaihatsu Jigyodan
Kanadevia Corp
Original Assignee
Agency of Industrial Science and Technology
Hitachi Zosen Corp
Shingijutsu Kaihatsu Jigyodan
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Agency of Industrial Science and Technology, Hitachi Zosen Corp, Shingijutsu Kaihatsu Jigyodan filed Critical Agency of Industrial Science and Technology
Priority to JP16087383A priority Critical patent/JPS6052691A/en
Publication of JPS6052691A publication Critical patent/JPS6052691A/en
Publication of JPS6354836B2 publication Critical patent/JPS6354836B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は例えばバガス(甘蔗の搾り滓)、竹、
ケナフ等の非木材繊維原料を75〜90%の高収率で
機械パルプ化する方法に関する。 バガスの高収率パルプ化法には多くの方法が提
案されている。中でも特開昭55−62288号公報で
示されているようにバガスを少量のアルカリ性薬
品を用いて前処理した後、加圧加熱状態で収率が
75〜90%と高く、且つ強度特性がすぐれているの
で、リフアイニングしてパルプ化するいわゆるC
―TMP法が新聞紙級筆記印刷紙の主原料パルプ
を製造するのに適していると言われている。とこ
ろで非木材繊維を少量のアルカリ性薬品を用いて
リフアイニングすると生成するパルプが非常に不
均一なものが生じる傾向がある。即ち、300メツ
シユの布を通過するものからスリツト巾0.15mm
のスクリーを通過しないものまで広い範囲に亘つ
てパルプが分布する。特に、スリツト巾0.15mmを
通過しないものは一般に結束繊維といわれるもの
で、抄造時紙切れが生じたり、またこれが最終紙
製品に含まれると、印刷時に紙表面からはがれる
などの問題が生じるので、これが含まれないよう
にしなければならない。そのためにリフアイナー
でくりかえして処理する段数を増加したり、リフ
アイナーの磨砕板の目を細くすることが一般に行
なわれるが、こうすると微細な繊維の割合も異常
に増加してパルプの水性が低下し紙抄造が困難
になるという問題が生じる。なお、一般に新聞紙
の主原料となる機械パルプのフリーネスは80〜
150mlCSF(カナダ標準フリーネス)が望ましいと
いわれている。 ところで、本発明者等は、バガス、竹、ケナフ
等の非木材繊維をリフアイナーにより機械的にパ
ルプ化する実験を行つた結果、次の知見を得た。
即ち、非木材繊維原料はリフアイナーで処理する
と容易に単繊維に分離される成分(軟質成分と称
す)から、なかなか単繊維への分離されにくい成
分(硬質成分と称す)まで広い範囲に分布してい
る。この軟質成分はアルカリ性薬液の存在下で前
処理の上機械的に処理すると上記単繊維に分離さ
れるばかりでなく、繊維の損傷を受け、微細繊維
片になつてパルプのフリーネスを異常に低下させ
る。一方、硬質成分は竪く剛直で無理にリフアイ
ナーで処理すると繊維が折れて粉未が生じるだけ
で、パルプ強度は非常に弱くなる性質がある。 そこで、本発明者等は、非木材繊維原料がこの
ようなリフアイナーによる機械的処理に対し異な
る特性を持つことに着目、検討した結果、従来の
問題を解消し得る非木材繊維原料の機械パルプ化
法を発明するに至つた。 即ち、非木材繊維原料をアルカリ性薬液の存在
下にて1次前処理し、次に加圧・加熱下にてデイ
スクリフアイナーで機械的に処理してフリーネス
250〜600mlCSFの中間パルプを得、次にこの中間
パルプを結束繊維を含まない細いパルプと結束繊
維を含む粗いパルプとにしかも細いパルプと粗い
パルプとの比が70:30〜50:50になるように分離
し、次に上記粗いパルプを更にアルカリ性薬液の
存在下にて2次前処理をなし且つこのときの1次
前処理と2次前処理におけるアルカリ性薬液の割
合をNa2O基準として6:1〜1:1の範囲で調
整し、次にこの2次前処理がなされた粗いパルプ
をデイスクリフアイナーで機械的に処理した後、
上記分離された細いパルプに混合することを特徴
とする非木材繊維原料の機械パルプ化法で、かか
る方法によると、フリーネスが高く(水性の良
い)、結束繊維が少なく、且つ強度の高い仕上り
パルプが得られ、従つてパルプから紙にするとき
の抄造性が良くなると共に紙製品の印刷適性が良
くなる。更に、繊維原料に対するリフアイニング
が効果的に行なわれるので、所要リフアイニング
動力が減少する。また、アルカリ性薬液の割合を
Na2O基準として6:1〜1:1の範囲に調整し
たので、粗いパルプに対する薬品前処理の効果を
向上させることができるとともに細いパルプの強
度の低下を防止することができる。 以下、本発明の一実施例を第1図に基づき説明
する。 まず、バガス、竹、ケナフ等の非木材繊維原料
をアルカリ性薬液の存在化にて加温保持(1次前
処理)する。なお、上記アルカリ性薬液として
は、アルカリ土類金属水酸化物(Ca(OH)2)、ア
ルカリ金属水酸化物(NaOH等)、炭酸塩
(Na2CO3)、亜硫酸塩(Na2SO3)等の単独又は
混合物が使用される。特に、NaOHとNa2SO3
の混合物を使用すると、強度が高く且つ白色度も
良いパルプが得られる。この場合、Na2OとSO2
との重量比が4:1〜1:1の範囲でしかも
Na2Oが非木材繊維原料の絶乾重量当り1〜5%
の範囲であることが望ましい。また、上記加温保
持は、次のリフアイニング工程と同じ蒸気加圧下
に行なうのが望ましい。次に、上記1次前処理さ
れた非木材繊維原料を加圧・加熱下にてデイスク
リフアイナーで機械的に処理してフリーネス250
〜600mlCSF(望ましくは300〜500mlCSF)の中間
パルプを得る。上記加圧・加熱は大気圧以上の圧
力を有する蒸気により行なわれ、その圧力範囲は
0.2〜3Kg/cm2(ゲージ圧)が望ましく、また温
度範囲は105〜140℃ご望ましい。なお、上記中間
パルプのフリーネスは250mlCSFより小さくなる
と、過度にリフアイニングされて300メツシユを
通過する微細繊維の割合が増加し、またフリーネ
スが600mlより大きくなると結束繊維の割合が増
加する。次に、上記中間パルプを、結束繊維を実
質的に含まない細いパイプと結束繊維を多く含む
粗いパルプとに分離する。上記分離はパルプ濃度
1〜2%の水溶液中でロータリスクリーン等を用
いて1段又は2段にて行なわれる。なお、細いパ
ルプと粗いパルプとの比は70:30〜50:50の範囲
内にあるのが望しい。この比より大きいと細いパ
ルプ中に結束繊維が許容量(通常1%以下といわ
れている)以上含まれる恐れがあり、またこの比
より小さいと粗いパルプの中にこれ以上のリフア
イニングの必要のない良好な繊維が多く含まれる
ことになる。次に、上記粗いパルプだけを再びア
ルカリ性薬液の存在下にて加温保持(2次前処
理)を行なう。なお、この場合、50〜100℃の大
気圧下で行なうのが良いが、100℃以上の加圧下
でもよい。場合によつては、1次前処理工程に粗
いパルプを戻すようにしてもよい。処理時間は通
常2〜60分である。また、上記2次前処理工程に
て使用されるアルカリ性薬液は1次前処理にて使
用されるアルカリ性薬液と同じものが用いられ、
また1次前処理及び2次前処理にて使用されるア
ルカリ性薬液の使用合計量は、もとの非木材繊維
に対し、Na2Oの量が1.5〜5%の範囲となるよう
にするのが望ましい。Na2Oの量が少ないと、硬
質成分が粉末化してパルプ強度が不足し、リフア
イニング動力が上昇する。またNa2Oの量が多す
ぎると、軟質成分が過度にリフアイニングされた
り、アルカリによる溶出が大きくなつて収率が低
下し、パルプの白色度、不透明が低下する。な
お、1次前処理と2次前処理とにおけるアルカリ
性薬液の使用割合は6:1〜1:1の範囲になる
のが望ましい。この比より大きいと粗いパルプに
対する薬品前処理の効果が少なくなり、またこの
比より小さいと細いパルプの強度が著しく低くな
り不都合となる。次に、2次前処理された粗いパ
ルプを、再び大気圧型デイスクリフアイナーで、
1段又は2段処理を行なう。なお、リフアイニン
グはパルプ濃度が10〜30%の範囲で行なうのが望
ましい。また、リフアイニング後のパルプは場合
によつては上記分離工程に戻すようにしてもよ
い。そして、分離工程で得られた細いパルプと、
上記リフアイニング工程で得られたパルプとを混
合し、また必要に応じて除塵や漂白を行なつて新
聞紙等の原料パルプを得る。 以上の方法によると、フリーネスが高く(水
性の良い)、結束繊維が少なく、且つ強度の高い
仕上りパルプが得られ、従つてパルプから紙にす
るときの抄造性が良くなると共に紙製品の印刷適
性が良くなる。更に、繊維原料に対するリフアイ
ニングが効果的に行なわれるので、所要のリフア
イニング動力が減少する。 次に、具体例について説明する。 Γ 具体例1 インドパシア産脱ピカバガス(さとうきびのし
ぼりかすからピス分を除去したもの)にアルカリ
性亜硫酸ナトリウムを脱ピスバガス絶乾重量基準
でNa2Oとして3.4%、SC2として1.2%を添加し、
スチームによつて予め120℃で4分間加熱処理し
てからデイスク径610mmの加圧型デイスクリフア
イナー120℃に維持した状態で1段のリフアイニ
ング処理を行つた。リフアイニング後のパルプの
フリーネスは350mlCSFであつた。次に、これを
水で希釈し、1.1%濃度のパルプ液にして2.2mmの
目穴をもつロータリスクリーンに供給し、スクリ
ーンを通過する細いパルプと通過しない粗いパル
プとに分離した。細いパルプと粗いパルプの比は
55:45であつた。この内粗いパルプにアルカリ性
亜硫酸ナトリウムをもとの脱ピスバガス絶乾重量
基準でNa2Oとして0.7%、SO2として0.3%添加
し、パルプ濃度5%、温度80℃で30分間保持して
前処理を行ない、その後パルプ濃度が20%になる
まで脱液してからデイスク径610mmの大気圧型デ
イスクリフアイナーに供給し、リフアイニング処
理を行つた。このリフアイニング処理パルプと細
いパルプとを合計したものはもとの脱ピスバガス
に対し83%の収率であつた。パルプ化テスト結果
は表―1に示す。 本発明の方法によるパルプ(試料No.5)と従来
法によるパルプ(試料No.6)を比較すると本発明
の本法によるパルプはフリーネスが高く結束繊維
含量が少なく、強度特性にすぐれている。また、
本発明の方法はリフアイニング動力は少ない。な
お、従来法によるパルプ(試料No.6)はNa2Oと
して4.1%、SO2として1.5%を用いて前処理した
後、加圧リフアイニングを行ない、そして分離す
ることなく引き続き大気圧リフアイニングを行な
つたものである。 Γ 具体例2 タイ国産脱ピスバガスにアルカリ性亜硫酸ナト
リウムを脱ピスバガス絶乾重量基準でNa2Oとし
て2.6%、SO2として0.8%を添加しスチームによ
つて、予め125℃で5分間加熱処理してからデイ
スク径610mmの加圧型デイスクリフアイナーで125
℃に維持した状態で1段のリフアイニング処理を
行つた。得られたパルプのフリーネスは470ml
CSFで結束繊維含量は10.2%であつた。リフアイ
ニング動力はもとのバガスに対してトン当り
900KWHであつた。次にこのリフアイニングパ
ルプを水で希釈し1%濃度のパルプ濃度にして
1.8mmの目穴をもつロータリスクリーンに供給し、
スクリーンを通過する細いパルプと通過しないパ
ルプとに分離した。細いパルプと粗いパルプの比
は60:40であつた。次にこの粗いパルプにアルカ
リ性亜硫酸ナトリウムをもとの脱ピスバガス絶乾
重量基準でNa2Oとして1%、SO2として0.3%添
加し、二軸式ミキサー内に供給しスチームで加温
しながらパルプ濃度15%、温度90℃で5分間撹拌
処理してからデイスク径610mmの大気圧型デイス
クリフアイナーに供給しリフアイニング処理を行
つた。このリフアイニング処理パルプと前記細い
パルプを合計したものはもとの脱ピスバガスに対
し86%の収率であつた。比較のため、上記粗いパ
ルプの上記アルカリ性添加前処理工程を省略して
リフアイニングを行つた。これらのパルプ化結果
を表―2に示す。 本発明の方法による粗いパルプを前処理後再度
リフアイニングしたパルプ(試料No.10)は結束繊
維が少なく、強度も高いが、比較例に示す前処理
なしで粗いパルプを再度リフアイニングしたパル
プ(試料No.11)はパルプの強度、特に裂断長で示
される引張り強度が著しく低い欠点を有する。
The present invention can be applied to, for example, bagasse (cane dregs), bamboo,
It relates to a method for mechanically pulping non-wood fiber raw materials such as kenaf with a high yield of 75-90%. Many methods have been proposed for high-yield pulping of bagasse. Among them, as shown in JP-A-55-62288, bagasse is pretreated with a small amount of alkaline chemicals and then heated under pressure to improve the yield.
It has a high strength of 75 to 90% and has excellent strength properties, so it is suitable for so-called C, which is refined into pulp by refining.
-The TMP method is said to be suitable for producing pulp, the main raw material for newsprint-grade writing and printing paper. However, when non-wood fibers are refined using a small amount of alkaline chemicals, the resulting pulp tends to be very non-uniform. In other words, the slit width is 0.15 mm from the one that passes through 300 mesh cloth.
Pulp is distributed over a wide range including those that do not pass through the screen. In particular, fibers that do not pass through a slit width of 0.15 mm are generally called binding fibers, which can cause paper breakage during papermaking, and if they are included in the final paper product, they can cause problems such as peeling off from the paper surface during printing. Must not be included. To this end, it is common practice to increase the number of stages of repeated processing in the refiner or to make the grinding plates of the refiner narrower, but this will abnormally increase the proportion of fine fibers and reduce the water content of the pulp. A problem arises in that paper manufacturing becomes difficult. Generally, the freeness of mechanical pulp, which is the main raw material for newspaper, is 80~
It is said that 150ml CSF (Canadian Standard Freeness) is desirable. By the way, the present inventors conducted an experiment in which non-wood fibers such as bagasse, bamboo, and kenaf were mechanically pulped using a refiner, and as a result, the following findings were obtained.
In other words, non-wood fiber raw materials are distributed over a wide range, from components that are easily separated into single fibers when treated with a refiner (referred to as soft components) to components that are difficult to separate into single fibers (referred to as hard components). There is. When this soft component is pretreated and mechanically treated in the presence of an alkaline chemical solution, it not only separates into the above-mentioned single fibers, but also damages the fibers and becomes fine fiber pieces, which abnormally reduces the freeness of the pulp. . On the other hand, hard components are vertical and rigid, and if they are forcibly treated with a refiner, the fibers will break and crumble will occur, resulting in a very weak pulp strength. Therefore, the present inventors focused on the fact that non-wood fiber raw materials have different characteristics when compared to the mechanical processing by such a refiner, and as a result of their studies, they found that mechanical pulping of non-wood fiber raw materials could solve the conventional problems. He came to invent a law. That is, the non-wood fiber raw material is first pretreated in the presence of an alkaline chemical solution, and then mechanically treated with a disc ironer under pressure and heat to achieve freeness.
Obtain an intermediate pulp of 250 to 600 ml CSF, and then divide this intermediate pulp into a fine pulp that does not contain binding fibers and a coarse pulp that contains binding fibers, and the ratio of the fine pulp to the coarse pulp is 70:30 to 50:50. Then, the coarse pulp is further subjected to a second pretreatment in the presence of an alkaline chemical solution, and the ratio of the alkaline chemical solution in the first pretreatment and the second pretreatment is 6 on the basis of Na 2 O. : Adjusted in the range of 1 to 1:1, and then the coarse pulp subjected to this secondary pretreatment was mechanically treated with a disk-cliff eyeliner.
A method of mechanically pulping a non-wood fiber raw material, which is characterized by mixing it with the separated thin pulp described above. According to this method, a finished pulp with high freeness (good aqueous property), low binding fibers, and high strength can be obtained. is obtained, thus improving the paper-making properties when making paper from pulp and improving the printability of paper products. Furthermore, since the fiber raw material is effectively refined, the required refining power is reduced. In addition, the proportion of alkaline chemical solution
Since the ratio is adjusted to a range of 6:1 to 1:1 based on Na 2 O, it is possible to improve the effect of chemical pretreatment on coarse pulp and prevent a decrease in the strength of fine pulp. An embodiment of the present invention will be described below with reference to FIG. First, non-wood fiber raw materials such as bagasse, bamboo, and kenaf are heated and maintained in the presence of an alkaline chemical solution (primary pretreatment). The alkaline chemicals mentioned above include alkaline earth metal hydroxides (Ca(OH) 2 ), alkali metal hydroxides (NaOH, etc.), carbonates (Na 2 CO 3 ), and sulfites (Na 2 SO 3 ). etc. may be used alone or in combination. In particular, when a mixture of NaOH and Na 2 SO 3 is used, a pulp with high strength and good whiteness can be obtained. In this case Na2O and SO2
and the weight ratio is in the range of 4:1 to 1:1 and
Na 2 O is 1-5% per bone dry weight of non-wood fiber raw material
It is desirable that it be within the range of . Further, it is desirable that the heating and holding is performed under the same steam pressure as the next refining step. Next, the non-wood fiber raw material that has undergone the first pretreatment is mechanically treated with a discreet eyeliner under pressure and heat to achieve a freeness of 250%.
Obtain an intermediate pulp of ~600 ml CSF (preferably 300-500 ml CSF). The above pressurization and heating are performed using steam with a pressure higher than atmospheric pressure, and the pressure range is
The desired temperature range is 0.2 to 3 Kg/cm 2 (gauge pressure) and the desired temperature range is 105 to 140°C. Note that when the freeness of the intermediate pulp becomes less than 250 ml CSF, the proportion of fine fibers that are excessively refined and pass through the 300 mesh increases, and when the freeness exceeds 600 ml, the proportion of bound fibers increases. Next, the intermediate pulp is separated into a thin pipe that does not substantially contain bound fibers and a coarse pulp that contains a large amount of bound fibers. The above separation is carried out in one or two stages using a rotary screen or the like in an aqueous solution having a pulp concentration of 1 to 2%. Note that the ratio of fine pulp to coarse pulp is preferably within the range of 70:30 to 50:50. If the ratio is larger than this, there is a risk that the fine pulp may contain more than the permissible amount of cohesive fibers (usually said to be less than 1%), and if the ratio is smaller than this, the coarse pulp may not require further refining. It will contain a lot of good fiber. Next, only the coarse pulp is heated and held again in the presence of an alkaline chemical solution (secondary pretreatment). In this case, it is preferable to carry out the reaction under atmospheric pressure of 50 to 100°C, but it may also be carried out under pressure of 100°C or higher. In some cases, coarse pulp may be returned to the primary pretreatment step. Processing time is usually 2 to 60 minutes. In addition, the alkaline chemical solution used in the second pretreatment step is the same as the alkaline chemical solution used in the first pretreatment step,
In addition, the total amount of alkaline chemicals used in the primary pretreatment and secondary pretreatment should be such that the amount of Na 2 O is in the range of 1.5 to 5% based on the original non-wood fiber. is desirable. If the amount of Na 2 O is small, the hard components will be powdered, the pulp strength will be insufficient, and the refining power will increase. In addition, if the amount of Na 2 O is too large, the soft components may be excessively refined, the elution by alkali will increase, the yield will decrease, and the whiteness and opacity of the pulp will decrease. Note that the ratio of the alkaline chemicals used in the primary pretreatment and the secondary pretreatment is preferably in the range of 6:1 to 1:1. If the ratio is larger than this, the effect of chemical pretreatment on coarse pulp will be reduced, and if the ratio is smaller than this ratio, the strength of fine pulp will be significantly lowered, which is disadvantageous. Next, the coarse pulp that has been subjected to the secondary pretreatment is again passed through an atmospheric pressure type disk clarifier.
Perform one-stage or two-stage processing. Note that refining is desirably carried out at a pulp concentration of 10 to 30%. Further, the pulp after refining may be returned to the above-mentioned separation step as the case may be. Then, the thin pulp obtained in the separation process,
The pulp obtained in the above-mentioned refining process is mixed, and if necessary, dust removal and bleaching are performed to obtain raw material pulp for newspapers and the like. According to the above method, a finished pulp with high freeness (good aqueous property), low binding fibers, and high strength can be obtained, which improves the formability when making paper from pulp and improves the printability of paper products. gets better. Furthermore, since the fiber raw material is effectively refined, the required refining power is reduced. Next, a specific example will be explained. Γ Specific example 1 Alkaline sodium sulfite is added to depissed picabagasse produced in Indopasia (from which the pis content has been removed from sugarcane residue), and 3.4% as Na 2 O and 1.2% as SC 2 are added based on the absolute dry weight of depissed bagasse.
After heat treatment with steam at 120° C. for 4 minutes, one-stage refining treatment was carried out using a pressurized disk stiffener with a disk diameter of 610 mm and maintained at 120° C. The freeness of the pulp after refining was 350 ml CSF. Next, this was diluted with water to make a pulp liquid with a concentration of 1.1%, and was supplied to a rotary screen with 2.2 mm holes to separate fine pulp that passed through the screen and coarse pulp that did not. The ratio of fine pulp to coarse pulp is
It was 55:45. Pretreatment was carried out by adding alkaline sodium sulfite to the coarse pulp and adding 0.7% as Na 2 O and 0.3% as SO 2 based on the original depissed bagasse bone dry weight, and holding the pulp at a pulp concentration of 5% and a temperature of 80°C for 30 minutes. After that, the pulp was deliquified until the pulp concentration reached 20%, and then fed to an atmospheric pressure type disc refining machine with a disc diameter of 610 mm to perform a refining process. The total yield of this refined pulp and fine pulp was 83% of the original depissed bagasse. The pulping test results are shown in Table-1. Comparing the pulp produced by the method of the present invention (Sample No. 5) and the pulp produced by the conventional method (Sample No. 6), the pulp produced by the method of the present invention has high freeness, low binding fiber content, and excellent strength properties. Also,
The method of the present invention requires less refining power. The pulp produced by the conventional method (sample No. 6) was pretreated with 4.1% Na 2 O and 1.5% SO 2 and then subjected to pressure refining, followed by atmospheric pressure refining without separation. It is something that has become familiar. Γ Specific example 2 Alkaline sodium sulfite was added to depissed bagasse produced in Thailand with 2.6% Na 2 O and 0.8% SO 2 based on the bone dry weight of the depissed bagasse, and heat treated with steam at 125°C for 5 minutes. 125 with a pressurized disk cliff eyeliner with a disk diameter of 610 mm.
A one-stage refining process was performed while maintaining the temperature at °C. The freeness of the obtained pulp is 470ml
The bound fiber content in CSF was 10.2%. Refining power per ton of original bagasse
It was 900KWH. Next, dilute this refined pulp with water to a pulp concentration of 1%.
Supplied to a rotary screen with 1.8mm eye holes,
The pulp was separated into a thin pulp that passed through the screen and a pulp that did not. The ratio of fine pulp to coarse pulp was 60:40. Next, alkaline sodium sulfite was added to this coarse pulp, based on the bone-dry weight of the original depissed bagasse, 1% as Na 2 O and 0.3% as SO 2 was added, and the mixture was fed into a twin-screw mixer and heated with steam to form the pulp. The mixture was stirred for 5 minutes at a concentration of 15% and a temperature of 90°C, and then fed to an atmospheric pressure disc refining machine with a disc diameter of 610 mm for refining. The total yield of this refined pulp and the thin pulp was 86% based on the original depissed bagasse. For comparison, the coarse pulp was subjected to refining without the alkaline addition pretreatment step. Table 2 shows these pulping results. The pulp (Sample No. 10) obtained by re-refining coarse pulp by the method of the present invention after pre-treatment has fewer bundled fibers and high strength, but the pulp obtained by re-refining coarse pulp without pre-treatment as shown in the comparative example (Sample No. .11) has the disadvantage that the strength of the pulp, especially the tensile strength indicated by the breaking length, is extremely low.

【表】【table】

【表】 ところで、具体例1において、1段目の加圧型
デイスクリフアイナーのプレート間隔を調節し、
リフアイニング動力を変えることにより各種フリ
ーネスの中間パルプを得た。次にロータリスクリ
ーンの入口濃度を調節して、この中間パルプを細
いパルプと粗いパルプとに55:45の比をほぼ維持
しながら分離した。中間パルプのフリーネスと細
いパルプのフリーネスおよび細いパルプ中の結束
繊維含量の関係を求めた。結果を第2図のグラフ
に示す。 リフアイニングを過度に行い中間パルプのフリ
ーネスを250mlCSF以下に低下させると細いパル
プのフリーネスは異常に低下し、一方リフアイニ
ングが不十分で中間パルプのフリーネスが600ml
CSFより高いと細いパルプ中の結束繊維含量が異
常に増加する不具合が生じた。 また、具体例2において、中間パルプの分離工
程で、ロータリースクリーンの目穴径を変えて分
離される細いパルプと粗いパルプの比を変えた。
粗いパルプのフリーネス及び細いパルプ中の結束
繊維含量を測定した結果を第3図のグラフに示
す。 細いパルプと粗いパルプの比が70:30より大き
いと細いパルプ中の結束繊維の割合が異常に増大
し不具合である。一方比が50:50より小さいと粗
いパルプのフリーネスが低下し粗いパルプ中にこ
れ以上リフアイニングの必要のない良好な繊維の
割合が増加すると判断された。
[Table] By the way, in Specific Example 1, the plate spacing of the first stage pressurized disc lift eyeer was adjusted,
By changing the refining power, intermediate pulps with various freenesses were obtained. The inlet concentration of the rotary screen was then adjusted to separate this intermediate pulp into fine and coarse pulps, maintaining approximately a 55:45 ratio. The relationship between the freeness of the intermediate pulp, the freeness of the fine pulp, and the content of bound fibers in the fine pulp was determined. The results are shown in the graph of FIG. If the reflining is performed excessively and the freeness of the intermediate pulp is reduced to below 250ml CSF, the freeness of the thin pulp will be abnormally reduced, while if the reflining is insufficient, the freeness of the intermediate pulp will be reduced to 600ml.
When the content was higher than CSF, a problem occurred in which the content of bound fibers in the thin pulp increased abnormally. Further, in Specific Example 2, in the intermediate pulp separation step, the ratio of fine pulp to coarse pulp to be separated was changed by changing the hole diameter of the rotary screen.
The results of measuring the freeness of the coarse pulp and the content of bound fibers in the fine pulp are shown in the graph of FIG. If the ratio of fine pulp to coarse pulp is greater than 70:30, the proportion of bound fibers in the fine pulp will abnormally increase, which is a problem. On the other hand, it was determined that when the ratio is smaller than 50:50, the freeness of the coarse pulp decreases and the proportion of good fibers that do not require further refining increases in the coarse pulp.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の一実施例の工程図、第2図は
中間パルプフリーネスに対する細いパルプフリー
ネス及び細いパルプ中の結束繊維含量を示すグラ
フ、第3図は細いパルプと粗いパルプとの比に対
する粗いパルプのフリーネス及び細いパルプ中の
結束繊維含量を示すグラフである。
Fig. 1 is a process diagram of an embodiment of the present invention, Fig. 2 is a graph showing fine pulp freeness relative to intermediate pulp freeness and binding fiber content in the fine pulp, and Fig. 3 is a graph showing the ratio of fine pulp to coarse pulp. 1 is a graph showing the freeness of coarse pulp and the bound fiber content in fine pulp.

Claims (1)

【特許請求の範囲】 1 非木材繊維原料をアルカリ性薬液の存在下に
て1次前処理し、次に加圧・加熱下にてデイスク
リフアイナーで機械的に処理してフリーネス250
〜600mlCSFの中間パルプを得、次にこの中間パ
ルプを結束繊維を含まない細いパルプと結束繊維
を含む粗いパルプとにしかも細いパルプと粗いパ
ルプとの比が70:30〜50:50になるように分離
し、次に上記粗いパルプを更にアルカリ性薬液の
存在下にて2次前処理をなし且つこのときの1次
前処理と2次前処理におけるアルカリ性薬液の割
合をNa2O基準として6:1〜1:1の範囲で調
整し、次にこの2次前処理がなされた粗いパルプ
をデイスクリフアイナーで機械的に処理した後、
上記分離された細いパルプに混合することを特徴
とする非木材繊維原料の機械パルプ化法。 2 アルカリ性薬液としてNaOHとNa2SO3の混
合物使用すると共に、Na2OとSO2との重量比が
4:1〜1:1の範囲でしかもNa2Oが非木材繊
維原料の絶乾重量当り1〜5%の範囲であること
を特徴とする特許請求の範囲第1項記載の非木材
繊維原料の機械パルプ化法。 3 粗いパルプを1次前処理工程に戻すことを特
徴とする特許請求の範囲第1項記載の非木材繊維
原料の機械パルプ化法。 4 粗いパルプをリフアイニングした後、再び分
離工程に戻すことを特徴とする特許請求の範囲第
1項記載の非木材繊維原料の機械パルプ化法。
[Scope of Claims] 1. A non-wood fiber raw material is first pretreated in the presence of an alkaline chemical solution, and then mechanically treated with a Discliff Eyener under pressure and heat to achieve a freeness of 250%.
Obtain ~600ml CSF of intermediate pulp, and then divide this intermediate pulp into a fine pulp that does not contain binding fibers and a coarse pulp that contains binding fibers, and the ratio of fine pulp to coarse pulp is 70:30 to 50:50. Next, the coarse pulp is further subjected to a second pretreatment in the presence of an alkaline chemical solution, and the ratio of the alkaline chemical solution in the first pretreatment and the second pretreatment is 6: After adjusting the ratio in the range of 1 to 1:1, and then mechanically treating this secondary pretreated coarse pulp with a disk stiffener,
A method for mechanically pulping a non-wood fiber raw material, which method comprises mixing the above-mentioned separated fine pulp. 2 A mixture of NaOH and Na 2 SO 3 is used as the alkaline chemical solution, and the weight ratio of Na 2 O and SO 2 is in the range of 4:1 to 1:1, and Na 2 O is less than the absolute dry weight of the non-wood fiber raw material. A method for mechanically pulping a non-wood fiber raw material according to claim 1, characterized in that the pulping amount is in the range of 1 to 5%. 3. A method for mechanical pulping of non-wood fiber raw materials according to claim 1, characterized in that the coarse pulp is returned to the first pretreatment step. 4. The method for mechanically pulping a non-wood fiber raw material according to claim 1, characterized in that after the coarse pulp is refined, it is returned to the separation step.
JP16087383A 1983-08-31 1983-08-31 Mechanical pulping method for non-wood fiber raw materials Granted JPS6052691A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16087383A JPS6052691A (en) 1983-08-31 1983-08-31 Mechanical pulping method for non-wood fiber raw materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16087383A JPS6052691A (en) 1983-08-31 1983-08-31 Mechanical pulping method for non-wood fiber raw materials

Publications (2)

Publication Number Publication Date
JPS6052691A JPS6052691A (en) 1985-03-25
JPS6354836B2 true JPS6354836B2 (en) 1988-10-31

Family

ID=15724211

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16087383A Granted JPS6052691A (en) 1983-08-31 1983-08-31 Mechanical pulping method for non-wood fiber raw materials

Country Status (1)

Country Link
JP (1) JPS6052691A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5562288A (en) * 1978-10-25 1980-05-10 Kogyo Gijutsuin Pulping of fiber material other than wood

Also Published As

Publication number Publication date
JPS6052691A (en) 1985-03-25

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