JP2850124B2 - Paper manufacturing method - Google Patents
Paper manufacturing methodInfo
- Publication number
- JP2850124B2 JP2850124B2 JP63031974A JP3197488A JP2850124B2 JP 2850124 B2 JP2850124 B2 JP 2850124B2 JP 63031974 A JP63031974 A JP 63031974A JP 3197488 A JP3197488 A JP 3197488A JP 2850124 B2 JP2850124 B2 JP 2850124B2
- Authority
- JP
- Japan
- Prior art keywords
- paper
- steam
- sizing agent
- sizing
- press
- 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 - Fee Related
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 238000004513 sizing Methods 0.000 claims description 34
- 239000003795 chemical substances by application Substances 0.000 claims description 24
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 11
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 claims description 11
- -1 ketene dimer compound Chemical class 0.000 claims description 11
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 claims description 11
- 150000003972 cyclic carboxylic anhydrides Chemical class 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 150000002430 hydrocarbons Chemical group 0.000 claims description 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 239000000123 paper Substances 0.000 description 55
- 238000001035 drying Methods 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 229920006395 saturated elastomer Polymers 0.000 description 8
- 239000013055 pulp slurry Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- WASQWSOJHCZDFK-UHFFFAOYSA-N diketene Chemical compound C=C1CC(=O)O1 WASQWSOJHCZDFK-UHFFFAOYSA-N 0.000 description 6
- 229920001131 Pulp (paper) Polymers 0.000 description 4
- 238000003825 pressing Methods 0.000 description 4
- 239000002023 wood Substances 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 229920006319 cationized starch Polymers 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000010893 paper waste Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 239000013054 paper strength agent Substances 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 229920006163 vinyl copolymer Polymers 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 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
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229940099112 cornstarch Drugs 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- NXLOLUFNDSBYTP-UHFFFAOYSA-N retene Chemical compound C1=CC=C2C3=CC=C(C(C)C)C=C3C=CC2=C1C NXLOLUFNDSBYTP-UHFFFAOYSA-N 0.000 description 1
- 102200150779 rs200154873 Human genes 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
Landscapes
- Paper (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明はサイズ剤を用いてサイズされた紙の製造方法
に関する。The present invention relates to a method for producing paper sized using a sizing agent.
紙は親水性のセルロース繊維素からできているため、
水、その他の流体をよく吸う性質を持っている。そのた
め水性インク等で筆記したり、印刷する場合、これのに
じみ止め、或いはインキ止めが必須であり、このための
サイジングが必要になる。周知のようにサイジングは紙
が液体を吸収する性質を押さえる、いわゆるサイズ性も
しくは耐水性を付与する他撥水性、防水性を紙に付与す
ることができる。このサイジングに用いるサイズ剤とし
ては従来よりロジン系サイズ剤が多用されているが、近
年酸性紙の劣化の問題もあって中性紙がクローズアップ
され、例えばケテンダイマー系水性分散液等の中性サイ
ズ剤が脚光を浴びてきた。Because paper is made of hydrophilic cellulose fiber,
It has the property of absorbing water and other fluids well. Therefore, when writing or printing with water-based ink or the like, it is essential to stop bleeding or stopping the ink, and sizing for this is required. As is well known, sizing suppresses the property of paper to absorb liquids, so-called sizing or water resistance, as well as water repellency and waterproofness. Rosin-based sizing agents have been frequently used as sizing agents for this sizing.However, recently, neutral paper has been brought up due to the problem of deterioration of acidic paper. Sizing agents are in the limelight.
しかしながらサイジングに於て多くのサイズ剤は多量
に使用し過ぎると紙や装置の汚れを生じ、少な過ぎると
サイズ効果が十分でないため、できる限り少量の使用で
所定のサイズ効果が得られるような有効な使用方法の開
発が望まれている。また中性サイズ剤として有用なケテ
ンダイマー系水性分散液の場合、紙匹形成後、ドライヤ
ーパートを通過した直後ではまだそのサイズレベルが低
いのが一般で、時間の経過と共に上昇してくるという傾
向がある。そのため、抄紙工程での作業性が低下し、品
質管理上の問題も発生しがちとなる。However, in sizing, if a large amount of sizing agent is used in a large amount, paper and equipment will be stained.If the amount is too small, the sizing effect will not be sufficient. It is desired to develop a new usage method. In addition, in the case of a ketene dimer-based aqueous dispersion useful as a neutral sizing agent, the size level is generally still low immediately after passing through the dryer part after forming the paper web, and tends to increase over time. There is. Therefore, the workability in the paper making process is reduced, and problems in quality control tend to occur.
又、抄紙工程中でサイズプレスを施す場合にも、サイ
ズプレス前のサイズ度が不十分なため、サイズプレス溶
液の吸液量が増大し、そのためサイズプレスした後の湿
紙の強度低下をきたし、紙きれ等のトラブルが発生する
他、サイズプレス後のドライヤーバートでの乾燥がうま
くいかないという問題点を生じる。In addition, when a size press is performed during the papermaking process, the degree of sizing before the size press is insufficient, so that the amount of liquid absorbed by the size press solution increases, and therefore the strength of the wet paper after the size press is reduced. In addition to problems such as paper breakage and the like, there is a problem that drying in a dryer bar after size pressing is not successful.
そこでそのような問題点を解決するため、ケテンダイ
マー系水性分散液に種々のカオチン性樹脂と併用する試
みがなされているが、(例えば特開昭48−48702号、特
開昭55−137296号、特開昭56−101998号等)まだ満足の
いく結果は得られていない。In order to solve such a problem, attempts have been made to use a ketene dimer-based aqueous dispersion in combination with various kinds of cationic resins (for example, JP-A-48-48702, JP-A-55-137296). And JP-A-56-101998) have not yet obtained satisfactory results.
本発明はかかる状況に鑑み上記問題点を解決した、今
迄にないサイズ度の立上りをよくしたサイズ効果の優れ
た紙を製造する方法を確立することを目的とするもので
ある。SUMMARY OF THE INVENTION The present invention has been made in view of the above circumstances, and has as its object to solve the above problems and to establish a method for producing paper having an unprecedented sizing degree and excellent sizing effect.
本発明者は上記目的を達成するため検討を重ねた結
果、種々の添加物を用いるという従来の方法とは全く異
なった、プレスパートでプレスされた後、とりわけドラ
イヤーパートで乾燥された後の紙を、サイズプレスより
前の場所でスチームに曝すという簡便で経済的な方法に
より、該目的を達成できることを見出し本発明に到達し
た。The present inventor has repeatedly studied to achieve the above object, and as a result, completely different from the conventional method of using various additives, paper after being pressed in a press part, especially after being dried in a dryer part. Was found to be able to achieve the object by a simple and economical method of exposing to a steam before the size press.
すなわち本発明は、サイズ剤を用いてサイズされた紙
を製造するに際して、プレスパートでプレスされた後の
場所であってサイズプレスより前の場所で紙をスチーム
に曝すことを特徴とする紙の製造方法を提供するもので
ある。That is, the present invention provides a method for producing paper sized using a sizing agent, wherein the paper is exposed to steam at a place after being pressed by a press part and before a size press. It is intended to provide a manufacturing method.
以下本発明を詳細に説明する。 Hereinafter, the present invention will be described in detail.
本発明で使用されるサイズ剤はケテンダイマー系化合
物、置換環状ジカルボン酸無水物、ロジン系サイズ剤、
アルケニルコハク酸塩等から選ばれた1種以上のサイズ
剤等であり、特に一般式(I)のケテンダイマー系化合
物が好ましい。The sizing agent used in the present invention is a ketene dimer compound, a substituted cyclic dicarboxylic anhydride, a rosin sizing agent,
It is one or more sizing agents selected from alkenyl succinates and the like, and a ketene dimer compound of the general formula (I) is particularly preferable.
ケテンダイマー系化合物は式(I) (ただし、式中R1,R2は炭素数8〜30の炭化水素基を表
わす)で示されるケテンダイマーを保護コロイド機能を
有する澱粉、特にカチオン化澱粉又はカチオン性もしく
は両性ビニル系共重合物を用いて必要により界面活性剤
の存在下水性連続相に分散せしめて得た水性分散液とし
て使用される。なお、これにサイズ発現を促進するカチ
オン性樹脂を添加して用いてもよい。The ketene dimer compound has the formula (I) (Wherein R 1 and R 2 represent a hydrocarbon group having 8 to 30 carbon atoms). A ketene dimer represented by the following formula: is a starch having a protective colloid function, particularly a cationized starch or a cationic or amphoteric vinyl copolymer. And used as an aqueous dispersion obtained by dispersing in an aqueous continuous phase in the presence of a surfactant as necessary. It should be noted that a cationic resin which promotes the size expression may be added to this.
置換環状ジカルボン酸無水物は特公昭53−28526号、
特開昭58−45731号、特開昭61−34298号に例示されてい
るような炭素数8〜30のαオレフィンを触媒の存在下で
加熱せしめて得られる異性化オレフィンに無水マレイン
酸を付加反応せしめたもので、使用直前にカチオン化澱
粉、イオン性ビニル共重合体、又は乳化剤により乳化し
て用いられる。Substituted cyclic dicarboxylic anhydride is JP-B-53-28526,
Addition of maleic anhydride to an isomerized olefin obtained by heating an α-olefin having 8 to 30 carbon atoms in the presence of a catalyst as exemplified in JP-A-58-45731 and JP-A-61-34298. It is reacted and used just before use by emulsifying with cationized starch, ionic vinyl copolymer or emulsifier.
ロジン系サイズ剤としてはガムロジン、ウッドロジン
もしくはトール油ロジン又はこれらをホルムアルデヒド
で加熱処理したロジン変性物を(無水)マレイン酸、フ
マル酸、アクリル酸、イタコン酸、シトラコン酸等の
α,β−不飽和酸と反応せしめた後、アルカリで中和し
た溶液型ロジンサイズ剤、或いは特開昭47−20402号、
特開昭53−133259号、特開昭52−77206号、特開昭61−1
08796号等に例示された乳化剤及び必要により溶剤を用
いて乳化したエマルジョン型サイズ剤を用いることがで
きる。アルケニルコハク酸塩はプロピレン、イソブチレ
ン、ブチレン等のオレフィンの2〜6量体に無水マレイ
ン酸を付加したものをアルカリ中で中和したものが用い
られる。As a rosin-based sizing agent, gum rosin, wood rosin or tall oil rosin or a rosin modified product obtained by heat-treating these with formaldehyde (anhydrous) is α, β-unsaturated with maleic acid, fumaric acid, acrylic acid, itaconic acid, citraconic acid, etc. After reacting with an acid, a solution-type rosin sizing agent neutralized with an alkali, or JP-A-47-20402,
JP-A-53-133259, JP-A-52-77206, JP-A-61-1
Emulsifying agents exemplified in 08796 and the like and, if necessary, an emulsion-type sizing agent emulsified using a solvent can be used. As the alkenyl succinate, a product obtained by adding maleic anhydride to a dimer to hexamer of olefin such as propylene, isobutylene or butylene and neutralizing the same with an alkali is used.
本発明の紙の製造方法には公知の製紙方法が適用され
る。すなわち、上記したサイズ剤を通常使用されている
填料、染料、定着剤、紙力剤等の他の添加物とともにパ
ルプスラリー中に撹拌混合する。この紙料はスクリーン
を通して抄紙工程に送られる。A known papermaking method is applied to the paper production method of the present invention. That is, the above-mentioned sizing agent is stirred and mixed into a pulp slurry together with other commonly used additives such as a filler, a dye, a fixing agent, and a paper strength agent. This stock is sent through a screen to the papermaking process.
抄紙工程(抄紙機)は通常ワイヤーパート、プレスパ
ート、ドライパートの3つの部門からできている。すな
わちワイヤーパートで紙層を形成し、プレスパートで搾
水され、ドライヤーパートで乾燥される。本発明ではプ
レスパートでプレスされた後、特にその後のドライパー
トで乾燥された紙をスチームに曝すことが最も重要であ
る。The paper making process (paper machine) is usually made up of three divisions: a wire part, a press part, and a dry part. That is, a paper layer is formed in the wire part, water is squeezed in the press part, and dried in the dryer part. In the present invention, it is most important that the paper that has been pressed in the press part and then dried in the subsequent dry part is exposed to steam.
なお、必要によりいったん乾燥した紙はサイズプレ
ス、ゲートロールコーター、ビルブレートコータ、キャ
レンダー等で表面処理され、再度乾燥される。Once dried, the paper is subjected to a surface treatment with a size press, a gate roll coater, a bill coater, a calender or the like, and then dried again.
本発明で使用するスチームは飽和蒸気あるいは加熱蒸
気のいずれでもよいが飽和蒸気が適している。またゲー
ジ圧としては0.1〜6Kg/cm2の蒸気圧を持つ飽和蒸気を利
用することができる。紙がスチームに曝される時間は特
に制限されないが、紙が受けるスチーム重量は乾燥紙1
重量部当り0.002〜0.4重量部が適している。The steam used in the present invention may be either saturated steam or heated steam, but saturated steam is suitable. As the gauge pressure, saturated steam having a steam pressure of 0.1 to 6 kg / cm 2 can be used. The time for which the paper is exposed to steam is not particularly limited, but the weight of steam received by the paper is 1 dry paper.
0.002 to 0.4 parts by weight per part by weight is suitable.
又、本発明で紙をスチームに曝す方法は特に制限され
ないが、プレスパート直前、プレスパートで水分プロフ
ァイルの調節及び/或いはプレスによる搾水性を向上さ
せるために用いられているスチームボックス(例えばデ
ブロナイザー;デブロンハーキュレス社製)が有効に使
用できる。Further, the method of exposing the paper to steam in the present invention is not particularly limited, but a steam box (for example, a debronizer; used for adjusting the moisture profile and / or improving water squeezing by the press immediately before the press part). Debron Hercules) can be used effectively.
紙をスチームに曝す場所は紙匹水分率が低いほうがよ
く、プレスパート後で且つドライヤーパート前か、ドラ
イヤーパート、或いはドライヤーパート後がよい。これ
らの中でドライヤーパート後が好ましい。ケテンダイマ
ー系化合物をサイズ剤として用い、サイズ発現が遅くサ
イズプレス溶液の吸液量が必要以上に増大している場合
は、ドライヤーパート後で且つサイズプレス前で紙をス
チームに曝すことが最も適している。The place where the paper is exposed to steam is preferably such that the moisture content of the paper is low, and it is better after the press part and before the dryer part, the dryer part, or after the dryer part. Of these, after the dryer part is preferred. If a ketene dimer compound is used as a sizing agent and the size development is slow and the absorption of the size press solution is unnecessarily increased, it is best to expose the paper to steam after the dryer part and before the size press. ing.
本発明で用いるパルプ原料としてはクラフトパルプ或
いはサルファイトパルプ等の晒あるいは未晒化学パル
プ、砕木パルプ、機械パルプ或いはサーモメカニカルパ
ルプ等の晒或いは未晒高収率パルプ、新聞古紙、雑誌古
紙、段ボール古紙、或いは脱墨古紙等の古紙パルプのい
ずれも使用することができる。Pulp raw materials used in the present invention include bleached or unbleached high-yield pulp such as bleached or unbleached chemical pulp, groundwood pulp, mechanical pulp, or thermomechanical pulp, such as kraft pulp or sulfite pulp, used paper, used paper for magazines, and corrugated cardboard. Either waste paper or waste paper pulp such as deinked waste paper can be used.
填料、染料、乾燥紙力向上剤、湿潤紙力向上剤、歩留
り向上剤などの添加物も必要に応じ使用することができ
る。Additives such as fillers, dyes, dry paper strength improvers, wet paper strength improvers, retention aids and the like can be used as needed.
又、サイズプレス、ゲートロールコーター、ビルブレ
ートコーター、キャレンダー等で澱粉、ポリビニルアル
コール、染料、コーティングカラー、表面サイズ剤、防
滑剤等を必要に応じ塗布することもできる。Further, starch, polyvinyl alcohol, dye, coating color, surface sizing agent, anti-slip agent and the like can be applied as required by a size press, gate roll coater, bill coater, calender or the like.
以下、本発明を実施例を挙げて具体的に説明するが本
発明はこれら実施例にのみ限定されるものではない。な
お、以下の実施例及び比較例中において%とあるのは特
に断りのない限り、固型分重量%を意味し、また填料、
薬品の添加量は、絶乾パルプ重量に対する固型分重量%
で示した。Hereinafter, the present invention will be described specifically with reference to examples, but the present invention is not limited to these examples. In the following Examples and Comparative Examples, “%” means solid content% by weight, unless otherwise specified.
The amount of chemicals added is the solid content% by weight based on the absolutely dry pulp weight.
Indicated by
実施例1 2.4%濃度のパルプスラリー[BKP L/N=8/2,カナディ
アン・スタンダード・フリーネス380ml]に重質炭酸カ
ルシウム(エスカロン1500,三共精粉社製)20%を添加
し、2分間撹拌後、カチオン化澱粉(ケートF,王子コー
ンスターチ社製)0.75%、硫酸バン±0.5%を順次添加
し更に2分間撹拌した。次いでパルプスラリー濃度を0.
24%に希釈後、ケテンダイマー系サイズ剤(ハーコンW,
デイック・ハーキュレス社製)0.1%、歩留り向上剤
(ハイレテン104,ディック・ハーキュレス社製)0.02%
を添加し、1分間撹拌した後、ノーブル・アンド・ウッ
ド社製手抄き装置にて坪量70g/m2の湿紙を得た。なお抄
紙pHは8.0であった。この湿紙を水分率59.0%になるま
でプレスした後、ドラムドライヤーで80℃,70秒間乾燥
した。乾燥直後、水分率4.0%の紙を得た。次いで乾燥
直後の紙にゲージ圧0.5Kg/cm2の飽和スチームを1秒間
吹きかけた。紙の水分率変化より、紙が受けたスチーム
重量は紙の絶乾重量当り0.003と計算された。Example 1 20% of heavy calcium carbonate (Escalon 1500, manufactured by Sankyo Seiko Co., Ltd.) was added to 2.4% pulp slurry [BKP L / N = 8/2, Canadian Standard Freeness 380 ml] and stirred for 2 minutes. Thereafter, 0.75% of cationized starch (Kate F, manufactured by Oji Cornstarch Co., Ltd.) and bansulfate ± 0.5% were sequentially added, and the mixture was further stirred for 2 minutes. Next, the pulp slurry concentration was reduced to 0.
After dilution to 24%, a ketene dimer sizing agent (Harcon W,
Dic Hercules) 0.1%, Yield improver (High Reten 104, Dick Hercules) 0.02%
After stirring for 1 minute, a wet paper having a basis weight of 70 g / m 2 was obtained with a hand-making apparatus manufactured by Noble & Wood. The papermaking pH was 8.0. The wet paper was pressed to a moisture content of 59.0%, and then dried at 80 ° C. for 70 seconds with a drum dryer. Immediately after drying, paper having a water content of 4.0% was obtained. Next, saturated steam having a gauge pressure of 0.5 kg / cm 2 was sprayed on the paper immediately after drying for 1 second. From the change in the moisture content of the paper, the steam weight received by the paper was calculated to be 0.003 per absolute dry weight of the paper.
スチームを吹きかけた直後及び7日後のステキヒトサ
イズ度を測定し、その結果を表1に示した。Immediately after and 7 days after spraying steam, the degree of Stekigt sizing was measured, and the results are shown in Table 1.
実施例2〜5 飽和スチームの吹きかける時間を10秒、60秒、180
秒、360秒間と変化させた以外は実施例1と同じ操作を
行った。紙が受けたスチーム重量及びサイズ度測定結果
を表1に示した。なお、実施例4は参考のため表4,7に
も示した。Examples 2 to 5 Saturated steam was sprayed for 10 seconds, 60 seconds, and 180 seconds.
The same operation as in Example 1 was performed except that the time was changed to seconds and 360 seconds. Table 1 shows the measurement results of the steam weight and sizing degree received by the paper. Example 4 is also shown in Tables 4 and 7 for reference.
比較例1 実施例1と同じ操作を行ったが、乾燥直後の紙にはス
チームを吹きかけなかった。その結果を表1,3,4,7に示
した。Comparative Example 1 The same operation as in Example 1 was performed, but steam was not sprayed on the paper immediately after drying. The results are shown in Tables 1, 3, 4, and 7.
実施例6〜9 ケテンダイマー系サイズ剤としてハーコン40C,(ディ
ック・ハーキュレス社製)0.15%を使用した以外は実施
例1〜4と同じ操作を行った。その結果を表2に示し
た。 Examples 6 to 9 The same operation as in Examples 1 to 4 was performed except that Harcon 40C, 0.15% (manufactured by Dick Hercules) was used as a ketene dimer sizing agent. The results are shown in Table 2.
比較例2 実施例6と同じ操作を行ったが、乾燥直後の紙にはス
チームを吹きかけなかった。その結果を表2に示した。Comparative Example 2 The same operation as in Example 6 was performed, but no steam was sprayed on the paper immediately after drying. The results are shown in Table 2.
実施例10〜12 ゲージ圧0.1,0.5,3.0Kg/cm2の飽和スチームを120秒間
吹きかけた以外は実施例1と同じ操作を行った。その結
果を表3に示した。 Examples 10 to 12 The same operation as in Example 1 was performed except that saturated steam having a gauge pressure of 0.1, 0.5, and 3.0 kg / cm 2 was sprayed for 120 seconds. Table 3 shows the results.
実施例13 スチームを吹きかける場所をプレス後で且つドライヤ
ーで乾燥する前とした以外は実施例4と同じ操作を行っ
た。その結果を表4に示した。 Example 13 The same operation as in Example 4 was performed, except that the place where steam was sprayed was after pressing and before drying with a dryer. Table 4 shows the results.
比較例3 スチームを吹きかける場所を、プレスをかける前の水
分率88.5%の湿紙とする以外は実施例1と同じ操作を行
った。その結果を表4に示した。Comparative Example 3 The same operation as in Example 1 was performed except that the place where steam was sprayed was wet paper having a moisture content of 88.5% before pressing. Table 4 shows the results.
実施例14,15 2.4%濃度のパルプスラリ[段ボール古紙、カナディ
アン・スタンダード・フリーネス480ml]に両性ポリア
クリルアミド系紙力増強剤(エピノックスDS510,ディッ
ク・ハーキュレス社製)0.4%を添加し、2分間撹拌し
た。 Examples 14, 15 0.4% of amphoteric polyacrylamide-based paper strength enhancer (Epinox DS510, manufactured by Dick Hercules) was added to 2.4% pulp slurry [recycled corrugated paper, Canadian Standard Freeness 480 ml], and the mixture was stirred for 2 minutes. .
次いでパルプスラリーを0.33%に希釈後、ケテンダイ
マー系サイズ剤(ハーコンW0.1%又はハーコン40℃0.15
%)を添加し、1分間撹拌した後、ノーブル・アンド・
ウッド社製手抄き紙装置にて、坪量80g/m2の湿紙を得
た。なお抄紙pHは7.0であった。この湿紙をプレス後ド
ラムドライヤーで110℃,60秒間乾燥した。乾燥後直ち
に、紙にゲージ圧0.5Kg/cm2の飽和スチームを60秒間吹
きかけた。その結果を表5に示した。Then, after diluting the pulp slurry to 0.33%, a ketene dimer sizing agent (Harcon W 0.1% or Harcon 40 ° C 0.15%)
%) And stirred for 1 minute, followed by Noble &
A wet paper having a basis weight of 80 g / m 2 was obtained using a hand-made paper machine manufactured by Wood Corporation. The papermaking pH was 7.0. This wet paper was dried with a drum dryer at 110 ° C. for 60 seconds after pressing. Immediately after drying, the paper was sprayed with saturated steam having a gauge pressure of 0.5 kg / cm 2 for 60 seconds. Table 5 shows the results.
比較例4,5 実施例14,15と同じ操作を行ったが、乾燥直後の紙に
はスチームを吹きかけなかった。その結果を表5に示し
た。Comparative Examples 4 and 5 The same operation as in Examples 14 and 15 was performed, but steam was not sprayed on the paper immediately after drying. Table 5 shows the results.
実施例16,17 パルプとしてNUKP,カナディアン・スタンダード・フ
リーネス490mlを使用した以外は実施例14,15と同じ操作
を行い、結果を表6に示した。 Examples 16 and 17 The same operations as in Examples 14 and 15 were carried out except that NUKP, Canadian Standard Freeness 490 ml was used as the pulp. The results are shown in Table 6.
比較例6,7 実施例16,17と同じ操作を行ったが、乾燥直後の紙に
はスチームを吹きかけなかった。その結果を表6に示し
た。Comparative Examples 6 and 7 The same operations as in Examples 16 and 17 were performed, but steam was not sprayed on the paper immediately after drying. Table 6 shows the results.
実施例18 サイズ剤として置換環状ジカルボン酸無水物(サイズ
A−20,ディック・ハーキュレス社製)0.1%を使用した
以外は実施例4と同じ操作を行った。その結果を表7に
示した。Example 18 The same operation as in Example 4 was performed except that 0.1% of substituted cyclic dicarboxylic anhydride (size A-20, manufactured by Dick Hercules) was used as a sizing agent. Table 7 shows the results.
比較例8 実施例18と同じ操作を行ったが、乾燥直後の紙にはス
チームを吹きかけなかった。その結果を表7に示した。Comparative Example 8 The same operation as in Example 18 was performed, but no steam was sprayed on the paper immediately after drying. Table 7 shows the results.
実施例19,20,21 2.4%濃度のパルプスラリー[BKP L/N=8/2,カナディ
アン・スタンダードフリーネス380ml]に溶液ロジンサ
イズ剤(PFP,ディック・ハーキュレス社製)0.5%また
はエマルジョン型ロジンサイズ剤(ニューフォー100,デ
ィック・ハーキュレス社製)0.5%、またはアルケニル
コハク酸塩(NSP,ミサワセラミックケミカル社製)0.5
%を添加し、次いで硫酸バン±2.0%添加し、2分間撹
拌した。次いでパルプスラリーを0.24%に希釈後、ポリ
アクリルアミド系紙力剤(エピノックスRS631,デイック
・ハーキュレス社製)を0.05%添加し、1分間撹拌した
後、ノーブル・アンド・ウッド手抄き装置にて坪量65g/
m2の湿紙を得た。なお抄紙pHは4.5であった。この湿紙
をプレス後、ドラムドライヤーで100℃,50秒間乾燥し
た。乾燥後直ちに紙にゲージ圧0.5Kg/cm2の飽和スチー
ムを60秒間吹きかけた。その結果を表8に示した。 Examples 19, 20, 21 0.5% solution rosin size (PFP, manufactured by Dick Hercules) or emulsion type rosin size in 2.4% pulp slurry [BKP L / N = 8/2, Canadian Standard Freeness 380 ml] 0.5% (Newfour 100, manufactured by Dick Hercules) or 0.5 alkenyl succinate (NSP, manufactured by Misawa Ceramic Chemicals)
%, Followed by sulphate ± 2.0% and stirred for 2 minutes. Next, after diluting the pulp slurry to 0.24%, a polyacrylamide-based paper strength agent (Epinox RS631, manufactured by Dick Hercules) was added at 0.05%, and the mixture was stirred for 1 minute, and then ground with a Noble & Wood hand-making apparatus. 65g /
m 2 wet paper was obtained. The papermaking pH was 4.5. After the wet paper was pressed, it was dried at 100 ° C. for 50 seconds with a drum dryer. Immediately after drying, the paper was sprayed with saturated steam having a gauge pressure of 0.5 kg / cm 2 for 60 seconds. Table 8 shows the results.
比較例9,10,11 実施例19,20,21と同じ走査を起ったが、乾燥直後の紙
にはスチームを吹きかけなかった。その結果を表8に示
した。Comparative Examples 9, 10, and 11 The same scanning as in Examples 19, 20, and 21 was performed, but no steam was sprayed on the paper immediately after drying. Table 8 shows the results.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭55−137293(JP,A) 特開 昭62−177277(JP,A) 特開 昭62−223388(JP,A) 特開 昭58−36296(JP,A) 特公 昭45−40682(JP,B1) (58)調査した分野(Int.Cl.6,DB名) D21H 17/00 - 17/74 D21F 7/00 - 11/00──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-55-137293 (JP, A) JP-A-62-177277 (JP, A) JP-A-62-223388 (JP, A) JP-A-58-1983 36296 (JP, A) JP 45-40682 (JP, B1) (58) Fields investigated (Int. Cl. 6 , DB name) D21H 17/00-17/74 D21F 7/00-11/00
Claims (3)
ボン酸無水物、ロジン系サイズ剤及びアルケニルコハク
酸塩から選ばれた1種以上のサイズ剤を用いてサイズさ
れた紙を製造するに際して、プレスパートでプレスされ
た後の場所であってサイズプレスより前の場所で紙をス
チームに曝すことを特徴とする紙の製造方法。A press part for producing paper sized using at least one sizing agent selected from a ketene dimer compound, a substituted cyclic dicarboxylic anhydride, a rosin sizing agent and an alkenyl succinate. Exposing the paper to steam at a location after being pressed in step (1) and before the size press.
が、ドライヤーパートで乾燥された後の場所であってサ
イズプレスより前の場所であることを特徴とする請求項
1記載の紙の製造方法。2. The paper according to claim 1, wherein the place after the paper is pressed in the press part is a place after the paper is dried in the dryer part and before the size press. Production method.
テンダイマー系化合物であることを特徴とする請求項1
記載の紙の製造方法。 (ただし、式(I)中R1及びR2はそれぞれ炭素数8〜30
の炭化水素基を表わす)。3. The sizing agent is a ketene dimer compound represented by the following general formula (I).
The method for producing the paper as described above. (However, R 1 and R 2 in the formula (I) each have 8 to 30 carbon atoms.
Represents a hydrocarbon group).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63031974A JP2850124B2 (en) | 1988-02-16 | 1988-02-16 | Paper manufacturing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63031974A JP2850124B2 (en) | 1988-02-16 | 1988-02-16 | Paper manufacturing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01207495A JPH01207495A (en) | 1989-08-21 |
| JP2850124B2 true JP2850124B2 (en) | 1999-01-27 |
Family
ID=12345922
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63031974A Expired - Fee Related JP2850124B2 (en) | 1988-02-16 | 1988-02-16 | Paper manufacturing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2850124B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4743657B2 (en) * | 2005-07-29 | 2011-08-10 | 荒川化学工業株式会社 | Paper sizing and printing paper |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55137293A (en) * | 1979-04-05 | 1980-10-25 | Tadao Imagawa | Sheet dehydrating method in paper making machine |
| JPS62177277A (en) * | 1986-01-28 | 1987-08-04 | デブロン−ヘラクレス インコ−ポレ−テツド | Supply of steam to perforated web |
| US4685221A (en) * | 1986-02-28 | 1987-08-11 | Thermo Electron - Web Systems, Inc. | Steam-shower apparatus and method of using same |
-
1988
- 1988-02-16 JP JP63031974A patent/JP2850124B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH01207495A (en) | 1989-08-21 |
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