JPH11247089A - Production of paper - Google Patents
Production of paperInfo
- Publication number
- JPH11247089A JPH11247089A JP5350698A JP5350698A JPH11247089A JP H11247089 A JPH11247089 A JP H11247089A JP 5350698 A JP5350698 A JP 5350698A JP 5350698 A JP5350698 A JP 5350698A JP H11247089 A JPH11247089 A JP H11247089A
- Authority
- JP
- Japan
- Prior art keywords
- pulp
- paper
- phenolic compound
- added
- cationic
- 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.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title abstract description 4
- 229920001131 Pulp (paper) Polymers 0.000 claims abstract description 34
- 125000002091 cationic group Chemical group 0.000 claims abstract description 22
- 239000000701 coagulant Substances 0.000 claims abstract description 22
- 150000002989 phenols Chemical class 0.000 claims abstract description 22
- 239000007787 solid Substances 0.000 claims abstract description 14
- 239000000945 filler Substances 0.000 claims description 16
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 15
- 229920001568 phenolic resin Polymers 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 12
- 229920000371 poly(diallyldimethylammonium chloride) polymer Polymers 0.000 claims description 9
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 6
- 230000007935 neutral effect Effects 0.000 abstract description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 2
- 239000000463 material Substances 0.000 abstract 3
- 239000000123 paper Substances 0.000 description 23
- 229920002401 polyacrylamide Polymers 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 239000005518 polymer electrolyte Substances 0.000 description 7
- 229920006317 cationic polymer Polymers 0.000 description 6
- 239000013055 pulp slurry Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 125000000129 anionic group Chemical group 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000005189 flocculation Methods 0.000 description 3
- 230000016615 flocculation Effects 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000007711 solidification Methods 0.000 description 3
- 230000008023 solidification Effects 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 230000009977 dual effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000011859 microparticle Substances 0.000 description 2
- 229920000867 polyelectrolyte Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920002488 Hemicellulose Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- NJSSICCENMLTKO-HRCBOCMUSA-N [(1r,2s,4r,5r)-3-hydroxy-4-(4-methylphenyl)sulfonyloxy-6,8-dioxabicyclo[3.2.1]octan-2-yl] 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)O[C@H]1C(O)[C@@H](OS(=O)(=O)C=2C=CC(C)=CC=2)[C@@H]2OC[C@H]1O2 NJSSICCENMLTKO-HRCBOCMUSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003657 drainage water Substances 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000010893 paper waste Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 208000016261 weight loss Diseases 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Paper (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、填料を内添する機
械パルプ及び/または脱墨パルプを含む中質紙、下級
紙、新聞紙等の中性及至アルカリ性領域での抄紙方法に
関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for making paper in a neutral or alkaline region such as medium paper, lower grade paper, newsprint and the like containing mechanical pulp and / or deinked pulp to which a filler is internally added.
【0002】[0002]
【従来の技術】木材資源の保護からパルプ使用量の節
約、及び印刷適性等の紙質の向上のため紙に填料を出来
るだけ多量に内添させることが求められている。また、
近年抄紙機の高速化が進み、紙のより効率的な生産が求
められている。即ち、抄紙機のワイヤ−上での歩留ま
り、ろ水性の改善は重要な課題である。さらに、機械パ
ルプ及び/または脱墨パルプを多量に含む中質紙、下級
紙に於いても、印刷適性などの点から填料を出来るだけ
多量に内添させることが求められている。また、従来こ
れ等中質紙、下級紙は酸性領域で抄造されて来たが、近
年中性及至アルカリ性領域で、しかも、填料を多量に内
添させることが求められている。2. Description of the Related Art It is required to add a filler as much as possible to paper in order to save wood resources, save pulp usage, and improve paper quality such as printability. Also,
In recent years, the speed of paper machines has been increased, and more efficient production of paper has been demanded. That is, the improvement of the yield and drainage on the wire of a paper machine is an important issue. Furthermore, even in the case of medium-grade paper and low-grade paper containing a large amount of mechanical pulp and / or deinked pulp, it is required to add a filler as much as possible from the viewpoint of printability. Conventionally, such medium- and low-grade papers have been made in the acidic region, but in recent years there has been a demand for the addition of a large amount of filler in the neutral or alkaline region.
【0003】従来の一般的な抄紙工程における歩留まり
向上方法は、硫酸バンドの添加に続いて比較的高分子量
で低カチオン電荷密度のポリアクリルアミドを添加する
シングルポリマーシステムが使用されていた。近年の抄
紙機の高速化、用紙の軽量化、環境保全のための流失原
料の最少化に対応するために、比較的低分子量で高電荷
密度のポリジアリルジメチルアンモニウムクロリドの添
加に続いて比較的高分子量で低カチオンあるいは低アニ
オン電荷密度のポリアクリルアミドを添加するデュアル
ポリマーシステム、特開昭62−191598号公報や
特開平1−92498号公報に示されている様な比較的
高分子量で低カチオン電荷密度のポリアクリルアミドあ
るいはカチオン性澱粉の添加に続いて、高アニオン電荷
密度の膨潤性粘度鉱物であるベントナイトあるいはコロ
イダルシリカを添加するマイクロパーティクルシステ
ム、米国特許第4,313,790号や特表平8−504
900号公報に示されるフェノールホルムアルデヒド樹
脂の添加に続いて、ポリエチレンオキサイドあるいはポ
リエチレングリコールグラフトポリアクリルアミドを添
加するノニオン系リテンションシステムが用いられてき
た。In a conventional method for improving the yield in a general papermaking process, a single polymer system in which a polyacrylamide having a relatively high molecular weight and a low cationic charge density is added subsequent to the addition of a sulfate band has been used. Following the addition of relatively low molecular weight and high charge density polydiallyldimethylammonium chloride to respond to recent paper machine speedups, paper weight reductions, and the minimization of runaway raw materials for environmental protection. Dual polymer system in which polyacrylamide having high molecular weight and low cation or low anion charge density is added, relatively high molecular weight and low cation as disclosed in JP-A-62-191598 and JP-A-1-92498. A microparticle system in which bentonite or colloidal silica, which is a swelling viscosity mineral having a high anionic charge density, is added following addition of charge density polyacrylamide or cationic starch, US Pat. 8-504
A nonionic retention system in which polyethylene oxide or polyethylene glycol-grafted polyacrylamide is added subsequent to the addition of a phenol formaldehyde resin disclosed in Japanese Patent Publication No. 900 is used.
【0004】しかしながら、機械パルプを含む紙料にお
いては、機械パルプ由来のヘミセルロース、溶存リグニ
ン、樹脂酸、脂肪酸などの溶存性高分子が抄紙系に多量
に存在するためにアニオン性の微粒子を使用するマイク
ロパーティクルシステムは効果がない。また、デュアル
ポリマーシステムの場合は、カチオン性の凝結剤を使用
するのでシングルポリマーシステムよりもろ水性は向上
するものの、歩留まりはそれほど向上しない。ノニオン
系リテンションシステムの場合は、凝集能が高いので歩
留まりはシングルポリマーシステムよりも向上するが、
繊維自身の比表面積を減少させられないのでろ水性はシ
ングルポリマーシステムと同程度であった。However, in paper stock containing mechanical pulp, anionic fine particles are used because dissolved polymers such as hemicellulose, dissolved lignin, resin acids, and fatty acids derived from mechanical pulp are present in a large amount in the papermaking system. Microparticle systems have no effect. Further, in the case of the dual polymer system, the use of a cationic coagulant improves the freeness compared to the single polymer system, but does not significantly improve the yield. In the case of the nonionic retention system, the yield is higher than that of the single polymer system due to the high cohesion ability,
Freeness was comparable to a single polymer system because the specific surface area of the fiber itself could not be reduced.
【0005】このように上述の方法では、中性及至アル
カリ性領域に於ける機械パルプ及び/または脱墨パルプ
を多量に含む紙料に対しては、歩留まり及びろ水性の改
善は充分ではなかいために、抄紙機のワイヤ−上での脱
水工程に於いて填料の可成りの部分がワイヤ−を通過し
て了い、ワイヤ−摩耗が増大しワイヤ−ライフが短くな
ること、循環白水の負荷や排水の負荷が高くなることな
どの問題が生じる。[0005] As described above, in the above-mentioned method, the improvement of the yield and drainage is not sufficient for a paper pulp containing a large amount of mechanical pulp and / or deinked pulp in the neutral and alkaline areas. In the dewatering process on the wire of the paper machine, a substantial portion of the filler has passed through the wire, increasing wire wear and shortening the wire life, loading and draining circulating white water. This causes problems such as an increase in the load on the device.
【0006】[0006]
【発明が解決しようとする課題】中性及至アルカリ性領
域に於ける機械パルプ及び/または脱墨パルプを多量に
含む紙料では、アニオン性溶解物が多量に存在するた
め、歩留まり、ろ水性を向上させることは容易ではな
い。本発明は、この様な系に於ける歩留り及びろ水性を
同時に改善することを課題とした。In a stock containing a large amount of mechanical pulp and / or deinked pulp in the neutral to alkaline range, the yield and the drainage are improved because a large amount of anionic dissolved matter is present. It's not easy. An object of the present invention is to simultaneously improve the yield and drainage in such a system.
【0007】[0007]
【課題を解決するための手段】本発明者等は、機械パル
プ及び/または脱墨パルプを30〜100重量%含むパ
ルプと填料から成る紙料に対して、カチオン性凝結剤、
フェノール系化合物、ノニオン性凝集剤をこの順序で添
加し、かつカチオン性凝結剤とフェノール系化合物の比
率が25:75〜75:25の範囲であると、歩留まり
及びろ水性の何れもが大幅に改善されることを見出だし
た。Means for Solving the Problems The present inventors have proposed a method for preparing a pulp comprising a mechanical pulp and / or a pulp containing 30 to 100% by weight of deinked pulp and a filler, by using a cationic coagulant,
When the phenolic compound and the nonionic flocculant are added in this order, and the ratio of the cationic coagulant to the phenolic compound is in the range of 25:75 to 75:25, both the yield and the drainage are significantly increased. It was found to be improved.
【0008】[0008]
【発明の実施の形態】本発明は、機械パルプ及び/また
は脱墨パルプを全パルプ成分を基準として30〜100
重量%含むパルプと填料から成り、固形分が0.1〜
1.5重量%で、pH6〜10を有する中性及びアルカ
リ性領域の紙料に対して、カチオン性凝結剤、フェノー
ル系化合物、ノニオン系凝集剤の順序で添加し、かつカ
チオン性凝結剤とフェノール系化合物の比率が25:7
5〜75:25の範囲であることを特徴とする抄紙方法
である。BEST MODE FOR CARRYING OUT THE INVENTION The present invention relates to a method for preparing mechanical pulp and / or deinked pulp from 30 to 100 parts by weight based on the total pulp component.
It is composed of pulp containing filler by weight and filler, and has a solid content of 0.1 to
1.5 weight%, to a neutral and alkaline range stock having a pH of 6 to 10, a cationic coagulant, a phenolic compound and a nonionic coagulant are added in this order, and the cationic coagulant and phenol are added. 25: 7
A papermaking method characterized by being in the range of 5 to 75:25.
【0009】この時、カチオン性凝結剤、フェノール系
化合物の添加順序を変えた場合、歩留まりは向上する
が、ろ水性はそれほど向上しないので薬品の添加順序は
重要である。At this time, when the order of adding the cationic coagulant and the phenolic compound is changed, the yield is improved, but the drainage is not so much improved, so the order of adding the chemicals is important.
【0010】本発明で使用するカチオン性凝結剤は、カ
チオン性を示す電解質であれば、特に限定されるもので
はないが、ポリジアリルジメチルアンモニウムクロライ
ド(pDADMAC)あるいはその誘導体、ジアリルジ
メチルアンモニウムクロライドと他のモノマーの共重合
体が最も好ましい。また、カチオン性ポリクリルアミ
ド、ポリエチレンイミン、ポリアミン等を単独またはp
DADMACと併用しても良い。このカチオン性凝結剤
は通常紙料に対して0.005〜0.5重量%で添加さ
れる。[0010] The cationic coagulant used in the present invention is not particularly limited as long as it is an electrolyte exhibiting cationic properties. However, polydiallyldimethylammonium chloride (pDADMAC) or a derivative thereof, diallyldimethylammonium chloride and others are used. Is most preferred. Further, cationic polyacrylamide, polyethyleneimine, polyamine or the like may be used alone or p
You may use together with DADMAC. The cationic coagulant is usually added at 0.005 to 0.5% by weight based on the stock.
【0011】本発明で使用されるフェノール系化合物と
してはフェノールホルムアルデヒド樹脂(PFR)が望
ましい。また、ノニオン性凝集剤としては、ポリエチレ
ンオキサイド(PEO)あるいはポリエチレングリコー
ル(PEG)がグラフト重合されているポリアクリルア
ミド(PAM)が望ましく、その分子量としては、80
0万〜1200万の範囲が望ましい。The phenolic compound used in the present invention is preferably a phenol formaldehyde resin (PFR). As the nonionic coagulant, polyacrylamide (PAM) in which polyethylene oxide (PEO) or polyethylene glycol (PEG) is graft-polymerized is desirable.
The range of 100,000 to 12,000,000 is desirable.
【0012】これらの3種の薬品は、紙料の固形分が
0.1〜1.5重量%に希釈された段階で、カチオン性
凝集剤、フェノール系化合物、ノニオン系凝集剤の順で
添加する必要がある。紙料の固形分が1.5%を超える
と十分な混合が行われず、部分的に紙料が凝集し、地合
の悪化を招く。また、紙料の固形分が0.1重量%未満
の場合は、薬品が紙に効果的に定着しないので、歩留ま
り及びろ水性は顕著には向上しない。また、3種の薬品
の添加順序を変更したり、2種以上の薬品を混合しても
所望の効果は得られない。These three chemicals are added in the order of cationic coagulant, phenolic compound and nonionic coagulant when the solid content of the stock is diluted to 0.1 to 1.5% by weight. There is a need to. When the solid content of the stock exceeds 1.5%, sufficient mixing is not performed, and the stock partially agglomerates, resulting in poor formation. On the other hand, when the solid content of the stock is less than 0.1% by weight, the chemical does not effectively fix to the paper, so that the yield and drainage are not significantly improved. Even if the order of adding the three chemicals is changed or two or more chemicals are mixed, the desired effect cannot be obtained.
【0013】本発明で使用する脱墨パルプ(DIP)と
しては、上質紙、中質紙、下級紙、新聞用紙等を原料故
紙とする通常の脱墨パルプであれは特に問題はない。機
械パルプとしては、砕木パルプ(GP)、リファイナー
パルプ砕木パルプ(RGP)、サーモメカニカルパルプ
(TMP)、ケミサーモメカニカルパルプ(CTM
P)、ケミグランドパルプ(CGP)、セミケミカルパ
ルプ(SCP)等が挙げられる。機械パルプ及び脱墨パ
ルプは全パルプ成分の30〜100重量%であることが
必要であるが、残りはクラフトパルプ(KP)、サルフ
ァイトパルプ(SP)の様な化学パルプ、或いは合成繊
維などが適時配合される。As the deinked pulp (DIP) used in the present invention, there is no particular problem as long as it is a normal deinked pulp made of high quality paper, medium quality paper, lower grade paper, newsprint and the like as waste paper. As mechanical pulp, groundwood pulp (GP), refiner pulp groundwood pulp (RGP), thermomechanical pulp (TMP), chemithermomechanical pulp (CTM)
P), chemical ground pulp (CGP), semi-chemical pulp (SCP) and the like. The mechanical pulp and the deinked pulp need to be 30 to 100% by weight of the total pulp component, but the rest is made of chemical pulp such as kraft pulp (KP) or sulfite pulp (SP) or synthetic fiber. It is blended as appropriate.
【0014】本発明で使用される填料としては、紙の内
添用填料として通常使用される重質炭酸カルシウム、軽
質炭酸カルシウム、タルク、クレー、カオリン、二酸化
チタン、合成シリカ、水酸化アルミニウム等の無機物、
ポリスチレン樹脂、尿素ホルムアルデヒド樹脂等の合成
高分子微粒子が例示され、これ等を2種以上組合わせて
用いてもよい。填料の添加量は全紙料の1〜30重量%
が望ましい。また、必要に応じて、紙力増強剤、サイズ
剤、染料、蛍光増白剤、消泡剤、ピッチコントロール
剤、スライムコントロール剤等を紙料に添加することも
可能である。The filler used in the present invention includes heavy calcium carbonate, light calcium carbonate, talc, clay, kaolin, titanium dioxide, synthetic silica, aluminum hydroxide and the like which are usually used as fillers for internal addition to paper. Inorganic matter,
Synthetic polymer fine particles such as polystyrene resin and urea-formaldehyde resin are exemplified, and these may be used in combination of two or more. The amount of filler added is 1 to 30% by weight of the total stock
Is desirable. If necessary, a paper strength enhancer, a sizing agent, a dye, a fluorescent whitening agent, an antifoaming agent, a pitch control agent, a slime control agent and the like can be added to the stock.
【0015】[0015]
【作用】ろ水性はパルプスラリーの比表面積が減少すれ
ばする程、向上することがTappi Enginee
ring Conference 1996で報告され
ている。一般的に、抄紙系のイオン強度を上昇させた
り、高分子電解質を添加すれば、パルプスラリー中に懸
濁・分散している個体表面の電気二重層の圧縮がおこ
り、個体粒子間のファンデルワールス力がクーロン力の
反発による力を上回るために、個体粒子の凝結や起こ
り、比表面積が減少する。更に、高分子量の凝結剤を添
加すれば、架橋凝集が起こり更にパルプスラリーの比表
面積は減少する。つまり、パルプスラリーの強い凝集を
引き起こせば起すほど、パルプスラリーの比表面積が減
少し、高いろ水性を得られる。本発明では、パルプスラ
リーにカチオン性高分子電解質を添加することにより、
カチオン性高分子電解質が固体粒子表面に吸着し固体粒
子の凝結が起こる。その後、フェノール系化合物の添加
により、フェノール系化合物は一般的な中性及びアルカ
リ抄紙のpHであるpH7〜9では部分的にフェノール
性水酸基が解離しているのでアニオン性を帯びており、
先に添加したカチオン性高分子電解質が固体表面に吸着
した部位に強固に吸着する。その後、ノニオン系凝集剤
を添加すると、パルプサスペンションの固体表面に強固
に吸着したフェノール系化合物とノニオン系凝集剤がフ
ェノール性水酸基とエチレングリコールモノマーユニッ
トのエーテル部と水素結合により架橋凝集を起こし強い
凝集を引き起こし、結果としてろ水性が向上する。According to the Tappi Engineer, the drainage water improves as the specific surface area of the pulp slurry decreases.
ring Conference 1996. In general, if the ionic strength of a papermaking system is increased or a polymer electrolyte is added, the electric double layer on the surface of the solid suspended and dispersed in the pulp slurry will be compressed, and the van der Since the Waals force exceeds the force due to the repulsion of the Coulomb force, solidification and solidification of solid particles occur, and the specific surface area decreases. Further, when a high molecular weight coagulant is added, cross-linking and aggregation occur, and the specific surface area of the pulp slurry further decreases. In other words, the more agglomerated the pulp slurry is, the more the specific surface area of the pulp slurry is reduced, and a higher drainage is obtained. In the present invention, by adding a cationic polymer electrolyte to the pulp slurry,
The cationic polyelectrolyte is adsorbed on the surface of the solid particles, and solidification of the solid particles occurs. Thereafter, by addition of the phenolic compound, the phenolic compound is anionic since the phenolic hydroxyl group is partially dissociated at pH 7 to 9, which is a general neutral and alkaline papermaking pH,
The previously added cationic polymer electrolyte is strongly adsorbed to the site adsorbed on the solid surface. Thereafter, when a nonionic flocculant is added, the phenolic compound and the nonionic flocculant strongly adsorbed on the solid surface of the pulp suspension cause cross-linking and flocculation due to hydrogen bonding with the phenolic hydroxyl group and the ether portion of the ethylene glycol monomer unit, resulting in strong flocculation And consequently the freeness is improved.
【0016】カチオン性高分子電解質の添加に引き続
き、フェノール系化合物を添加する時に、フェノール系
化合物が過剰に存在すると、固体表面に吸着したカチオ
ン性高分子電解質の多くに吸着することにより、電気二
重層の圧縮が期待したほど起こらないために、凝結の程
度が弱く、ろ水性は向上しない。逆に、フェノール系化
合物の添加量がカチオン性高分子電解質の添加量よりも
比較的低い場合には、フェノール系化合物のほとんどの
フェノール性水酸基がカチオン性高分子電解質のカチオ
ン部位に吸着してしまい、その後に添加されるノニオン
系凝集剤と水素結合を形成できないので、凝集の程度が
減少し、その結果としてろ水性が向上しないものと考え
られ、カチオン性高分子電解質とフェノール系化合物に
は適切な添加比率が存在するものと考えられる。When the phenolic compound is excessively added when the phenolic compound is added subsequent to the addition of the cationic polymer electrolyte, the phenolic compound is adsorbed on a large amount of the cationic polymer electrolyte adsorbed on the solid surface, and the electric power is reduced. Since the compression of the overlay does not occur as expected, the degree of coagulation is weak and the freeness does not improve. Conversely, if the addition amount of the phenolic compound is relatively lower than the addition amount of the cationic polymer electrolyte, most of the phenolic hydroxyl groups of the phenolic compound will be adsorbed to the cation site of the cationic polymer electrolyte. Since it cannot form hydrogen bonds with the nonionic flocculant added afterwards, it is thought that the degree of flocculation is reduced and consequently the freeness is not improved, which is suitable for cationic polyelectrolytes and phenolic compounds. It is considered that there is a large addition ratio.
【0017】[0017]
【実施例】[実施例1]填料及び微細繊維の歩留まりの
測定は、ダイナミックドレネージジャー(DDJ)を使
用し TAPPI T261pm−79に従って行っ
た。DDJテスト時の撹拌速度は1,000rpmで、
200メッシュのワイヤーを使用して行った。紙料はD
IPが60%、晒TMPが20%、晒GPが10%、N
BKPが10%、填料としてPCCがパルプに対して1
0%配合されている0.5%のものを使用した。この紙
料をDDJに加え、15秒撹拌後に、硫酸バンドを絶乾
紙料に対して0.5%濃度で添加して15秒撹拌し、p
DAMAC(商品名:Alcofix、アライドコロイ
ド社製)とPFR(住友精化株式会社製)の合計添加量
が0.25% 〜0.2%で、しかも、pDADMAC
/PFR比が1:1になるように、まず、pDADMA
Cを添加して15秒撹拌し、その後PFRを添加し、最
後にPEO(PEO−27、住友精化株式会社製)を
0.015%添加して15秒撹拌し、1分間ろ水した。
このろ液の固形分濃度を測定し、填料及び微細繊維の歩
留まりを計算した。EXAMPLES [Example 1] The measurement of the yield of fillers and fine fibers was performed according to TAPPI T261 pm-79 using a dynamic drainage jar (DDJ). The stirring speed at the time of the DDJ test was 1,000 rpm,
This was performed using a 200 mesh wire. The stock is D
60% IP, 20% bleached TMP, 10% bleached GP, N
BKP is 10%, PCC as filler is 1 to pulp
0.5% of 0% was used. This stock was added to DDJ, and after stirring for 15 seconds, a sulfuric acid band was added at a concentration of 0.5% to the absolutely dry stock and stirred for 15 seconds.
The total addition amount of DAMAC (trade name: Alcofix, manufactured by Allied Colloids) and PFR (manufactured by Sumitomo Seika Co., Ltd.) is 0.25% to 0.2%.
First, pDADMA so that the / PFR ratio becomes 1: 1.
C was added and stirred for 15 seconds, and then PFR was added. Finally, 0.015% of PEO (PEO-27, manufactured by Sumitomo Seika Co., Ltd.) was added, stirred for 15 seconds, and filtered for 1 minute.
The solids concentration of this filtrate was measured, and the yield of filler and fine fibers was calculated.
【0018】ろ水度の測定には、填料及び微細繊維の歩
留まりの測定で使用した紙料を600mlを取り出し
1,000mlに希釈し、パルプ濃度を0.3%にし
て、ファイン歩留まりの測定と同様に1,000rpm
で撹拌し15秒撹拌後に、硫酸バンドを絶乾紙料に対し
て0.5%濃度で添加して15秒撹拌し、pDAMAC
とPFRの合計添加量が0.25% 〜0.2%で、し
かも、pDADMACとPFRの比率が50:50にな
るように、まず、pDADMACを添加して15秒攪拌
し、その後PFRを添加し、最後にPEOを0.015
%添加して15秒撹拌した後、T227 om−85に
従ってパルプのろ水度を測定した。To measure the freeness, 600 ml of the stock used in the measurement of the filler and fine fiber yield was taken out, diluted to 1,000 ml, the pulp concentration was set to 0.3%, and the fine yield was measured. Similarly, 1,000 rpm
After stirring for 15 seconds, a sulfuric acid band was added at a concentration of 0.5% with respect to the absolutely dry paper stock, followed by stirring for 15 seconds, and pDAMAC.
First, pDADMAC is added and stirred for 15 seconds so that the total added amount of PDADMAC and PFR is 0.25% to 0.2% and the ratio of pDADMAC to PFR is 50:50, and then PFR is added. And finally add PEO to 0.015
% And stirred for 15 seconds, and the freeness of the pulp was measured according to T227 om-85.
【0019】[実施例2]実施例1と同様の条件で、p
DADMACとPFRの比率を75:25で行った。[Embodiment 2] Under the same conditions as in Embodiment 1, p
The ratio of DADMAC to PFR was 75:25.
【0020】[実施例3]実施例1と同様の条件で、p
DADMACとPFRの比率を25:75で行った。[Embodiment 3] Under the same conditions as in Embodiment 1, p
The ratio of DADMAC to PFR was 25:75.
【0021】[比較例1]実施例1と同様の条件で、p
DADMACとPFRの比率を100:0で行った。Comparative Example 1 Under the same conditions as in Example 1, p
The ratio between DADMAC and PFR was 100: 0.
【0022】[比較例2]実施例1と同様の条件で、p
DADMACとPFRの比率を0:100で行った。Comparative Example 2 Under the same conditions as in Example 1, p
The ratio of DADMAC to PFR was 0: 100.
【0023】[比較例3]実施例1と同様の条件で、P
FRとpDADMACの添加順序を逆にして行った。Comparative Example 3 Under the same conditions as in Example 1, P
The order of addition of FR and pDADMAC was reversed.
【0024】[0024]
【表1】 [Table 1]
【0025】表1より、械パルプ及び脱墨パルプを主体
とする、中性及至アルカリ性の紙料に対して、カチオン
性凝結剤、フェノール系化合物、ノニオン性凝集剤をこ
の順序で添加し、かつカチオン性凝結剤とフェノール系
化合物の比率が25:75〜75:25の範囲であれ
ば、歩留まり及びろ水性は向上する。According to Table 1, a cationic coagulant, a phenolic compound and a nonionic coagulant are added in this order to neutral or alkaline paper stock mainly composed of mechanical pulp and deinked pulp, and When the ratio of the cationic coagulant to the phenolic compound is in the range of 25:75 to 75:25, the yield and drainage are improved.
【0026】[0026]
【発明の効果】本発明の抄紙方法により、歩留まり及び
ろ水性の何れもが大幅に改善される。According to the papermaking method of the present invention, both the retention and drainage are greatly improved.
Claims (4)
パルプ成分を基準として30〜100重量%含むパルプ
と填料を主成分とし、固形分が0.1〜1.5重量%
で、pH6〜10を有する紙料に対して、カチオン性凝
結剤、フェノール系化合物、ノニオン性凝集剤をこの順
序で添加し、かつカチオン性凝結剤とフェノール系化合
物の比率が25:75〜75:25の範囲であることを
特徴とする抄紙方法。1. A pulp containing mechanical pulp and / or deinked pulp in an amount of 30 to 100% by weight based on all pulp components and a filler as a main component, and a solid content of 0.1 to 1.5% by weight.
The cationic coagulant, the phenolic compound and the nonionic coagulant are added in this order to the stock having a pH of 6 to 10, and the ratio of the cationic coagulant to the phenolic compound is 25:75 to 75. : A papermaking method characterized by being in the range of 25.
ルアンモニウムクロリドであることを特徴とする請求項
1に記載の抄紙方法。2. The papermaking method according to claim 1, wherein the cationic coagulant is polydiallyldimethylammonium chloride.
アルデヒド樹脂(PFR)であることを特徴とする請求
項1又は2に記載の抄紙方法。3. The papermaking method according to claim 1, wherein the phenolic compound is a phenol formaldehyde resin (PFR).
イドであることを特徴とする請求項1、2又は3に記載
の抄紙方法。4. The papermaking method according to claim 1, wherein the nonionic flocculant is polyethylene oxide.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP05350698A JP3942723B2 (en) | 1998-03-05 | 1998-03-05 | Paper making method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP05350698A JP3942723B2 (en) | 1998-03-05 | 1998-03-05 | Paper making method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH11247089A true JPH11247089A (en) | 1999-09-14 |
| JP3942723B2 JP3942723B2 (en) | 2007-07-11 |
Family
ID=12944719
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP05350698A Expired - Fee Related JP3942723B2 (en) | 1998-03-05 | 1998-03-05 | Paper making method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3942723B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011094284A (en) * | 2009-09-30 | 2011-05-12 | Nippon Paper Industries Co Ltd | Method for producing paper |
| CN115652683A (en) * | 2022-11-21 | 2023-01-31 | 江苏富淼科技股份有限公司 | Papermaking method and papermaking system |
-
1998
- 1998-03-05 JP JP05350698A patent/JP3942723B2/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011094284A (en) * | 2009-09-30 | 2011-05-12 | Nippon Paper Industries Co Ltd | Method for producing paper |
| CN115652683A (en) * | 2022-11-21 | 2023-01-31 | 江苏富淼科技股份有限公司 | Papermaking method and papermaking system |
| CN115652683B (en) * | 2022-11-21 | 2024-05-10 | 江苏富淼科技股份有限公司 | Papermaking method and papermaking system |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3942723B2 (en) | 2007-07-11 |
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