JPH0215668B2 - - Google Patents
Info
- Publication number
- JPH0215668B2 JPH0215668B2 JP1258185A JP1258185A JPH0215668B2 JP H0215668 B2 JPH0215668 B2 JP H0215668B2 JP 1258185 A JP1258185 A JP 1258185A JP 1258185 A JP1258185 A JP 1258185A JP H0215668 B2 JPH0215668 B2 JP H0215668B2
- Authority
- JP
- Japan
- Prior art keywords
- pulp
- refining
- formula
- acid
- sodium
- 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
Links
- 238000007670 refining Methods 0.000 claims description 19
- 238000010009 beating Methods 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 7
- 229910052708 sodium Inorganic materials 0.000 claims description 7
- 239000002023 wood Substances 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 125000001174 sulfone group Chemical group 0.000 claims description 2
- 229920001131 Pulp (paper) Polymers 0.000 description 12
- 239000012752 auxiliary agent Substances 0.000 description 9
- 239000000835 fiber Substances 0.000 description 8
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 8
- 239000000123 paper Substances 0.000 description 7
- 239000011734 sodium Substances 0.000 description 6
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 239000000654 additive Substances 0.000 description 4
- 235000010265 sodium sulphite Nutrition 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- KSVSZLXDULFGDQ-UHFFFAOYSA-M sodium;4-aminobenzenesulfonate Chemical compound [Na+].NC1=CC=C(S([O-])(=O)=O)C=C1 KSVSZLXDULFGDQ-UHFFFAOYSA-M 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229960003080 taurine Drugs 0.000 description 3
- BHMLFPOTZYRDKA-IRXDYDNUSA-N (2s)-2-[(s)-(2-iodophenoxy)-phenylmethyl]morpholine Chemical compound IC1=CC=CC=C1O[C@@H](C=1C=CC=CC=1)[C@H]1OCCNC1 BHMLFPOTZYRDKA-IRXDYDNUSA-N 0.000 description 2
- VMSLCPKYRPDHLN-UHFFFAOYSA-N (R)-Humulone Chemical compound CC(C)CC(=O)C1=C(O)C(CC=C(C)C)=C(O)C(O)(CC=C(C)C)C1=O VMSLCPKYRPDHLN-UHFFFAOYSA-N 0.000 description 2
- OKAUOXITMZTUOJ-UHFFFAOYSA-N 7-aminonaphthalene-2-sulfonic acid Chemical compound C1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 OKAUOXITMZTUOJ-UHFFFAOYSA-N 0.000 description 2
- 238000004134 energy conservation Methods 0.000 description 2
- 239000011121 hardwood Substances 0.000 description 2
- 239000002655 kraft paper Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 2
- NRZRRZAVMCAKEP-UHFFFAOYSA-N naphthionic acid Chemical compound C1=CC=C2C(N)=CC=C(S(O)(=O)=O)C2=C1 NRZRRZAVMCAKEP-UHFFFAOYSA-N 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- QDWYPRSFEZRKDK-UHFFFAOYSA-M sodium;sulfamate Chemical compound [Na+].NS([O-])(=O)=O QDWYPRSFEZRKDK-UHFFFAOYSA-M 0.000 description 2
- 239000011122 softwood Substances 0.000 description 2
- 229950000244 sulfanilic acid Drugs 0.000 description 2
- ZMCHBSMFKQYNKA-UHFFFAOYSA-N 2-aminobenzenesulfonic acid Chemical compound NC1=CC=CC=C1S(O)(=O)=O ZMCHBSMFKQYNKA-UHFFFAOYSA-N 0.000 description 1
- FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
- ZAJAQTYSTDTMCU-UHFFFAOYSA-N 3-aminobenzenesulfonic acid Chemical compound NC1=CC=CC(S(O)(=O)=O)=C1 ZAJAQTYSTDTMCU-UHFFFAOYSA-N 0.000 description 1
- GEHMBYLTCISYNY-UHFFFAOYSA-N Ammonium sulfamate Chemical compound [NH4+].NS([O-])(=O)=O GEHMBYLTCISYNY-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- BPHHNXJPFPEJOF-UHFFFAOYSA-J chembl296966 Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]S(=O)(=O)C1=CC(S([O-])(=O)=O)=C(N)C2=C(O)C(N=NC3=CC=C(C=C3OC)C=3C=C(C(=CC=3)N=NC=3C(=C4C(N)=C(C=C(C4=CC=3)S([O-])(=O)=O)S([O-])(=O)=O)O)OC)=CC=C21 BPHHNXJPFPEJOF-UHFFFAOYSA-J 0.000 description 1
- 230000001010 compromised effect Effects 0.000 description 1
- IQFVPQOLBLOTPF-HKXUKFGYSA-L congo red Chemical compound [Na+].[Na+].C1=CC=CC2=C(N)C(/N=N/C3=CC=C(C=C3)C3=CC=C(C=C3)/N=N/C3=C(C4=CC=CC=C4C(=C3)S([O-])(=O)=O)N)=CC(S([O-])(=O)=O)=C21 IQFVPQOLBLOTPF-HKXUKFGYSA-L 0.000 description 1
- 239000000982 direct dye Substances 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- BTAAXEFROUUDIL-UHFFFAOYSA-M potassium;sulfamate Chemical compound [K+].NS([O-])(=O)=O BTAAXEFROUUDIL-UHFFFAOYSA-M 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- QPILZZVXGUNELN-UHFFFAOYSA-M sodium;4-amino-5-hydroxynaphthalene-2,7-disulfonate;hydron Chemical compound [Na+].OS(=O)(=O)C1=CC(O)=C2C(N)=CC(S([O-])(=O)=O)=CC2=C1 QPILZZVXGUNELN-UHFFFAOYSA-M 0.000 description 1
- UOOVFPYJUPSROO-UHFFFAOYSA-M sodium;naphthalene-1-sulfinate Chemical compound [Na+].C1=CC=C2C(S(=O)[O-])=CC=CC2=C1 UOOVFPYJUPSROO-UHFFFAOYSA-M 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000003351 stiffener Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Paper (AREA)
Description
本発明は高歩留パルプを製造する際、あるいは
パルプを叩解する際に、解繊又は叩解の電力消費
を節減する方法に関するものである。
近年リフアイナー砕木パルプ(RGP)、サーモ
メカニカルパルプ(TMP)、ケミグラウンドパル
プ(CGP)、セミケミカルパルプ(SCP)など高
歩留パルプは、新聞用紙、雑誌用紙、下級印刷用
紙の主原料として重要な地位を占めている。
RGPは、針葉樹チツプをデイスクリフアイナー
にかけてその摩砕力で解繊してパルプをつくる。
TMPは、同じく加圧下で(場合によつては、
亜硫酸ソーダーや亜硫酸水素ナトリウムによるチ
ツプの前処理を伴つた)デイスクリフアイナーで
解繊してつくる。CGPやSCPは、広葉樹チツプ
を亜硫酸ナトリウムや水酸化ナトリウムで組織を
軟化した後デイスクリフアイナーで繊維化してつ
くるパルプである。これらパルプは、木材チツプ
から単繊維への解繊はデイスクリフアイナーによ
る機械的作用で行なわれる。
このための電力消費量は、化学パルプを製造す
る場合に、200〜300KWH/tonであるのに対し、
高歩留パルプを製造する場合は、RGP1500〜
1800KWH/ton、TMP2000〜2200KWH/ton、
CGP1100〜1200KWH/ton、SCP600〜
800KWH/tonと極めて高く省エネルギーの点か
らこの電力節減が大きな問題になつている。
一方化学パルプは、未晒及び晒クラフトパルプ
を中心にほとんどの場合リフアイナーにより機械
処理を行つた上で抄紙する。この叩解により繊維
は、水和膨潤が進み抄紙に際し繊維同志の結合が
進行し優れた特性の紙となるため、叩解は欠くこ
とができない工程であり、ここでも、紙の種類に
より異なるが、電力消費は200〜4000KWH/ton
に及ぶ。
従来これらの電力消費を減らす方法として種種
の方法が考えられており、たとえばコンゴーレツ
ドやシカゴブルー6Bの様な直接染料をパルプに
加えて叩解する方法(Centola;製紙用繊維の基
礎と実際)や、カルボキシメチルセルロースやカ
ルボキシメチルでん粉を加えてリフアイニングす
る方法(特開昭56−61092号)が知られている。
しかしながら前者は薬品価格が高くパルプが赤や
青に染色されるため、実用化されることなく実験
室的な興味に終つている。また後者は添加時に泡
が発生し、そのまゝでは実操業に適用しにくい場
合がある。
本発明者らは高歩留パルプの解繊又は化学パル
プの叩解の際の電力消費をよりいつそう低減させ
ることを目的に研究を進めた結果、上記解繊又は
叩解の時に、何ら設備を変更することなくごく少
量添加することによつて更に効果的に目的を達す
ることの出来るリフアイニング助剤を見出し、本
発明をなすに至つた。
すなわち本発明は、木材チツプから高歩留パル
プを製造するために機械的解繊をする際、又はパ
ルプを叩解する際に、リフアイニング助剤として
同一分子内にスルホン基とアミノ基を有する下記
の一般式で示される化合物又はアミノリグノスル
ホン酸を添加し、その後機械的な解繊又は叩解を
行なうことを特徴とする木材チツプ又はパルプの
リフアイニング方法に関するものである。
一般式 H2N(−X)−oSO3Y
但しXはCH2、
The present invention relates to a method for reducing power consumption during defibration or beating when producing high-yield pulp or beating pulp. In recent years, high-yield pulps such as refined groundwood pulp (RGP), thermomechanical pulp (TMP), chemical ground pulp (CGP), and semi-chemical pulp (SCP) have become important as main raw materials for newsprint, magazine paper, and lower-grade printing paper. occupies a position.
RGP creates pulp by defibrating softwood chips using a disc grinder and using the grinding force of the grinding force. TMP is also under pressure (in some cases,
It is made by defibrating the chips with a discliff eyener (which involves pre-treatment of the chips with sodium sulfite or sodium hydrogen sulfite). CGP and SCP are pulps made by softening the tissue of hardwood chips with sodium sulfite or sodium hydroxide, and then turning them into fibers with discliner. These pulps are defibrated from wood chips into single fibers by the mechanical action of a disk stiffener. The power consumption for this is 200 to 300 KWH/ton when manufacturing chemical pulp, but
When producing high yield pulp, RGP1500~
1800KWH/ton, TMP2000~2200KWH/ton,
CGP1100~1200KWH/ton, SCP600~
The power consumption is extremely high at 800KWH/ton, and from the point of view of energy conservation, this power saving has become a major issue. On the other hand, chemical pulp, mainly unbleached and bleached kraft pulp, is processed mechanically using a refiner in most cases before being made into paper. Beating is an indispensable process because the fibers undergo hydration and swelling and bonding between fibers progresses during paper making, resulting in paper with excellent properties. Consumption is 200-4000KWH/ton
It extends to. Conventionally, various methods have been considered to reduce these power consumptions, such as adding direct dyes such as Congo Red and Chicago Blue 6B to the pulp and beating it (Centola; Fundamentals and Practice of Paper Manufacturing Fibers); A method of refining by adding carboxymethyl cellulose or carboxymethyl starch (Japanese Unexamined Patent Publication No. 1983-61092) is known.
However, the former method has high chemical costs and the pulp is dyed red or blue, so it has never been put to practical use and remains a laboratory interest. In addition, the latter generates bubbles when added, so it may be difficult to apply it to actual operations as it is. The present inventors conducted research with the aim of further reducing power consumption during defibration of high-yield pulp or beating of chemical pulp, and as a result, they made no changes to the equipment during the defibration or beating of chemical pulp. The present inventors have discovered a refining aid that can more effectively achieve the objective by adding a very small amount of the refining aid without adding any additives, and have accomplished the present invention. That is, the present invention uses the following refining aid having a sulfone group and an amino group in the same molecule when mechanically defibrating or beating pulp to produce high-yield pulp from wood chips. The present invention relates to a method for refining wood chips or pulp, which comprises adding a compound represented by the general formula or aminolignosulfonic acid, followed by mechanical defibration or beating. General formula H 2 N(-X)- o SO 3 Y where X is CH 2 ,
【式】【formula】
【式】
のいずれかを表わし、YはH、Na、K、NH4の
いずれかを表わす。又nは0〜2を表わす。
本発明の高歩留パルプとは、パルプ製造の際に
機械的に解繊する必要のあるパルプを言い、
RGP、TMP、CGP、SCPなどがあげられる。
又、本発明において叩解の際にリフアイニング
助剤が加えられるパルプとは、主としてクラフト
パルプ、サルフアイトパルプ、ソーダパルプをは
じめとする化学パルプを言うが、SCP等の高歩留
パルプであつても抄紙前に更に叩解を必要とする
場合には、本発明において「叩解の際にリフアイ
ニング助剤が加えられるパルプ」に含まれること
はもちろんである。
本発明に用いられるリフアイニング助剤として
は上記した一般式の化合物およびアミノリグノス
ルホン酸があげられるが、中でも好ましいものと
してはスルフアミン酸、タウリン、スルフアニル
酸、o−又はm−アミノベンゼンスルホン酸、ア
ミノリグノスルホン酸、ナフチオン酸、δ酸
([Formula] represents any one of the following, and Y represents any one of H, Na, K, and NH 4 . Further, n represents 0 to 2. The high-yield pulp of the present invention refers to pulp that needs to be mechanically defibrated during pulp production,
Examples include RGP, TMP, CGP, and SCP. In addition, in the present invention, the pulp to which a refining aid is added during beating mainly refers to chemical pulps such as kraft pulp, sulfite pulp, and soda pulp, but even high-yield pulps such as SCP can be used. If further beating is required before papermaking, it is of course included in the "pulp to which a refining aid is added during beating" in the present invention. Examples of the refining aid used in the present invention include compounds of the above general formula and aminolignosulfonic acid, but among them, sulfamic acid, taurine, sulfanilic acid, o- or m-aminobenzenesulfonic acid, and aminolignosulfonic acid are preferred. Lignosulfonic acid, naphthionic acid, delta acid (
【式】)、α酸 ([Formula]), alpha acid (
【式】)、 H酸(【formula】), H acid (
【式】)及びそれ
らのNa、K、NH4塩があげられる。
これらのリフアイニング助剤は単独で用いるこ
とも出来るし、また二種以上を混合して用いるこ
とももちろん可能である。リフアイニング助剤の
添加量はチツプ又はパルプの絶乾重量当り0.03〜
1%、好ましくは0.05〜0.5%である。
リフアイニング助剤の添加場所は本発明の目的
を達成することが出来るところであれば良く特に
制限されないが、RGPでは、チツプと共にリフ
アイナー入口に、TMPでは、チツプとともにプ
レヒーテイングチユーブ又は1次リフアイナー入
口に、CGPやSCPでは、薬品によるチユーブの
前処理装置に、又はリフアイナーの入口に添加さ
れるのが好ましい。化学パルプの叩解には、リフ
アイナーに入る前にパルプと助剤を均一に混合で
きる場所に加えるのが望ましい。
以上のように本発明は少量のリフアイニング助
剤を加えるのみで設備的には何ら変更を必要とせ
ずにリフアイナーの電力消費量を大巾に低減させ
ることが出来るものであり、又同一の電力を用い
た場合にはパルプの生産量や処理量を大巾に増や
すことが可能となるものである。いずれの場合に
もパルプの品質はいささかもそこなわれることは
ない。従つて本発明は紙パルプ工業にとつて特に
省エネルギーという点できわめて重要なものであ
る。
実施例 1
針葉樹チツプ600gを水とともに濃度15%でデ
イスクリフアイナーでフリーネス130mlにリフア
イニングした。この時助剤としてスルフアミン酸
ナトリウム、スルフアミン酸カリウム、スルフア
ニル酸ナトリウムを各0.3%(対絶乾チツプ重量)
デイスクリフアイナー入口に添加した。又比較の
ため無添加のものについて試験した。
各々についてリフアイニング電力、パルプ歩
留、パルプの結束繊維量を求め60g/m2に手抄し
て裂断長、引裂強度を求めた。
結果を第1表に示す。[Formula]) and their Na, K, NH 4 salts. These refining aids can be used alone or in combination of two or more. The amount of refining aid added is 0.03 to 0.03 per bone dry weight of chips or pulp.
1%, preferably 0.05-0.5%. The location of adding the refining aid is not particularly limited as long as it can achieve the purpose of the present invention, but in RGP, it is added at the refiner inlet together with the chips, and in TMP, it is added at the preheating tube or primary refiner entrance together with the chips. , CGP and SCP, it is preferably added to the pretreatment device of the tube with chemicals or at the inlet of the refiner. For refining chemical pulp, it is desirable to add the pulp and auxiliary agents at a location where they can be uniformly mixed before entering the refiner. As described above, the present invention can greatly reduce the power consumption of the refiner by adding a small amount of refining auxiliary agent without requiring any changes to the equipment. If used, it will be possible to greatly increase the amount of pulp produced and processed. In either case, the quality of the pulp is not compromised in the slightest. Therefore, the present invention is of great importance to the pulp and paper industry, especially from the point of view of energy conservation. Example 1 600 g of coniferous wood chips were refined to 130 ml of freeness with water and descliff eyeliner at a concentration of 15%. At this time, sodium sulfamate, potassium sulfamate, and sodium sulfanilate were added as auxiliary agents at 0.3% each (based on absolute dry chip weight).
Added to the diskcliff einer inlet. For comparison, a sample without additives was also tested. For each, the refining power, pulp yield, and amount of bundled fibers of the pulp were determined, and the pulp was hand-papered to 60 g/m 2 to determine the tear length and tear strength. The results are shown in Table 1.
【表】
実施例 2
針葉樹チツプ600gを4オートクレーブに詰
め、これに亜硫酸ナトリウム2%及び助剤を添加
し液比4で120℃、10分間処理した。助剤として
はスルフアミン酸、スルフアニル酸、タウリン、
ナフチオン酸を各0.2%添加した。又比較のため
無添加のものについて試験した。
前処理の終つたチツプは、デイスクリフアイナ
ーでフリーネス100mlに解繊した。この時のリフ
アイニング電力を求め、又得られたパルプの歩
留、結束繊維量、裂断長を求めた。
結果を第2表に示す。[Table] Example 2 600 g of softwood chips were packed into a 4 autoclave, 2% sodium sulfite and auxiliary agents were added thereto, and the mixture was treated at 120°C for 10 minutes at a liquid ratio of 4. Auxiliary agents include sulfamic acid, sulfanilic acid, taurine,
Naphthionic acid was added at 0.2% each. For comparison, a sample without additives was also tested. After the pretreatment, the chips were defibrated to 100 ml of freeness using a disk-cliffing iner. The refining power at this time was determined, and the yield of the obtained pulp, amount of bundled fibers, and tearing length were determined. The results are shown in Table 2.
【表】
実施例 3
広葉樹チツプ700gを4オートクレーブに詰
め、これに亜硫酸ナトリウム10%、炭酸ナトリウ
ム1%助剤0.1%(何れも対絶乾チツプ重量)添
加し液比3で、170℃、15分間処理した。前処理
の終つたチツプはその後デイスクリフアイナーで
フリーネス300mlに解繊した。
助剤としてはスルフアミン酸ナトリウム、スル
フアニル酸ナトリウム、アミノリグノスルホン酸
ナトリウム、δ酸ナトリウム、H酸ナトリウム、
α酸ナトリウムを用いた。又比較のため助剤無添
加で同様の試験を行つた。
各々のリフアイニング電力、歩留、結束繊維
量、裂断長を第3表に示す。[Table] Example 3 700g of hardwood chips were packed into 4 autoclaves, and 10% sodium sulfite, 1% sodium carbonate, and 0.1% auxiliary agent (all relative to absolute dry chip weight) were added at a liquid ratio of 3, at 170°C, 15°C. Processed for minutes. After the pretreatment, the chips were defibrated to 300 ml of freeness using a disk-cliffing iner. As auxiliary agents, sodium sulfamate, sodium sulfanilate, sodium aminolignosulfonate, sodium δ acid, sodium hydrate,
Sodium alpha acid was used. For comparison, a similar test was conducted without adding any auxiliary agent. Table 3 shows the refining power, yield, binding fiber amount, and tearing length for each.
【表】
実施例 4
NBKP30%、LBKP70%からなるパルプを絶
乾で30g相当とり助剤0.2%添加して濃度10%で
PFIミルによりフリーネス200mlまで叩解した。
助剤としてスルフアミン酸アンモニウム、タウ
リン、スルフアニル酸ナトリウム、アミノリグノ
スルホン酸ナトリウム、及びナフチオン酸ナトリ
ウムを用いた。又、比較のため助剤無添加のもの
について試験した。
この時のPFIミルの回転数及び得られたパルプ
の裂断長、引裂強さを求めた。
この結果を第4表に示す。[Table] Example 4 The equivalent of 30g of pulp consisting of 30% NBKP and 70% LBKP was taken in absolute dry condition and 0.2% of auxiliary agent was added to make the pulp 10%.
It was beaten to a freeness of 200ml using a PFI mill. Ammonium sulfamate, taurine, sodium sulfanilate, sodium aminolignosulfonate, and sodium naphthionate were used as auxiliaries. In addition, for comparison, a test was conducted with no additives added. At this time, the rotation speed of the PFI mill, the tear length and tear strength of the obtained pulp were determined. The results are shown in Table 4.
【表】
る。
[Table]
Claims (1)
に機械的解繊をする際、又はパルプを叩解する際
に、リフアイニング助剤として同一分子内にスル
ホン基とアミノ基を有する下記の一般式で示され
る化合物又はアミノリグノスルホン酸を添加し、
その後機械的な解繊又は叩解を行なうことを特徴
とする木材チツプ又はパルプのリフアイニング方
法。 一般式 H2N(−X)−oSO3Y 但しXはCH2、【式】 【式】 【式】のいずれかを表わし、 YはH、Na、K、NH4のいずれかを表わす。
又、nは0〜2を表わす。[Claims] 1. A refining aid having a sulfone group and an amino group in the same molecule, used as a refining aid during mechanical defibration to produce high-yield pulp from wood chips or when pulp is beaten. Adding a compound represented by the following general formula or aminolignosulfonic acid,
A method for refining wood chips or pulp, which comprises subsequently mechanically defibrating or beating the wood chips or pulp. General formula H 2 N (-X) - o SO 3 Y where X represents CH 2 , [Formula] [Formula] [Formula], and Y represents either H, Na, K, or NH 4 .
Further, n represents 0 to 2.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1258185A JPS61174492A (en) | 1985-01-28 | 1985-01-28 | Refining of wood chip or pulp |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1258185A JPS61174492A (en) | 1985-01-28 | 1985-01-28 | Refining of wood chip or pulp |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61174492A JPS61174492A (en) | 1986-08-06 |
| JPH0215668B2 true JPH0215668B2 (en) | 1990-04-12 |
Family
ID=11809319
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1258185A Granted JPS61174492A (en) | 1985-01-28 | 1985-01-28 | Refining of wood chip or pulp |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61174492A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0437900U (en) * | 1990-07-23 | 1992-03-31 |
-
1985
- 1985-01-28 JP JP1258185A patent/JPS61174492A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0437900U (en) * | 1990-07-23 | 1992-03-31 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61174492A (en) | 1986-08-06 |
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