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JPH0423036B2 - - Google Patents
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JPH0423036B2 - - Google Patents

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Publication number
JPH0423036B2
JPH0423036B2 JP26585987A JP26585987A JPH0423036B2 JP H0423036 B2 JPH0423036 B2 JP H0423036B2 JP 26585987 A JP26585987 A JP 26585987A JP 26585987 A JP26585987 A JP 26585987A JP H0423036 B2 JPH0423036 B2 JP H0423036B2
Authority
JP
Japan
Prior art keywords
deinking
group
pulp
ink
carbon atoms
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 - Lifetime
Application number
JP26585987A
Other languages
Japanese (ja)
Other versions
JPH01111086A (en
Inventor
Yoshitaka Myauchi
Koji Hamaguchi
Hideaki Urushibata
Masaaki Iwahashi
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP62265859A priority Critical patent/JPH01111086A/en
Publication of JPH01111086A publication Critical patent/JPH01111086A/en
Publication of JPH0423036B2 publication Critical patent/JPH0423036B2/ja
Granted legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/64Paper recycling

Landscapes

  • Paper (AREA)

Description

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

〔産業上の利用分野〕 本発明は新聞、雑誌等の古紙再生時に用いられ
る脱墨剤に関する。更に詳しくは新聞、雑誌等を
フロテーシヨン法で脱墨処理するに際し、高白色
度のそしてオフセツトインキに由来する残インキ
数の少ない脱墨パルプ、特に未剥離インキ数の少
ない脱墨パルプを得るための古紙再生用脱墨剤に
関する。 〔従来の技術及び問題点〕 新聞、雑誌等の再生利用は古くから行われて来
ているが、特に最近はその重要性を増して来てお
り、更に脱墨パルプの用途も高度利用への要請が
高まつてきている。一方、最近の古紙は印刷技
術、印刷方式の変化、印刷インキ成分の変化、軽
量化等、脱墨という観点から見れば一層険しい状
況となりつつあり、より以上脱墨を促進させるた
め装置にも改良が加えられて来ている。 古紙からインキその他の不純物を分離除去する
ため従来から用いられて来た薬剤としては苛性ソ
ーダ、珪酸ソーダ、リン酸ソーダ等のアルカリ
剤、過酸化水素、次亜硫酸塩、次亜塩素酸塩等の
漂白剤、DTPA、EDTA等の金属イオン封鎖剤
等があり、これらの薬剤と共に脱墨剤としてアル
キルベンゼンスルホン酸塩、高級アルコール硫酸
エステル塩、α−オレフインスルホン酸塩、ジア
ルキルスルホサクシネート等の陰イオン活性剤、
高級アルコール、アルキルフエノールのEO付加
物、EO・PO付加物及びアルカノールアマイド類
等の非イオン活性剤が単体又は2種以上配合され
て使用されて来た。しかしこれらの脱墨剤ではフ
ロテーシヨン処理におけるインキ分離除去能が小
さく、その為優れたインキ凝集能を有する脱墨剤
の開発が要望されて来た。 また、古紙からインキを完全に分離離脱するこ
とが難しく、特に最近の様に脱墨パルプの用途拡
大、配合比率の増大に伴つて古紙から離脱してい
ないインキ、即ち未剥離インキの存在が問題にな
りつつあり、更にインキ離脱性に優れた脱墨剤の
開発が要望されてきている。 〔問題点を解決するための手段〕 そこで、本発明者等は古紙からのインキ離脱力
に優れ、更にフロテーシヨン処理工程においては
離脱インキを気泡に吸着させパルプ繊維から分離
除去し、高白色度且つ低残インキ数の脱墨パル
プ、特に低未剥離インキの脱墨パルプを得ること
ができる脱墨剤を開発すべく鋭意研究した結果、
本発明を完成した。 即ち本発明は、 (a) 一般式(1)で表される化合物 R1COO−(AO)−oR2 ……(1) (式(1)中、R1は置換基としてOH基を有してい
てもよい炭素数7〜21のアルキル基又はアルケ
ニル基、R2はH又は炭素数1〜22のアルキル
基、アルケニル基ないしはアシルを表し、AO
は炭素数2〜4のオキシアルキレン基を表し、
nは全体の分子量が2000以下となる数である。) 及び (b) 天然油脂と多価アルコールとアルキレンオキ
シドとの反応生成物 を重量比で(a)/(b)=70/30〜5/95の割合で混合
してなる古紙再生用脱墨剤を提供するものであ
る。 本発明に係る一般式(1)で表される化合物は臨界
的であつて、これに類似する化合物であつても一
般式(1)の化合物に該当しないものは本発明の顕著
な効果は得られない。従つて、一般式(1)で示され
る官能基の限定、数値は極めて重要である。例え
ば、R1COO−基に代え、R1O−基(R1は一般式
(1)の条件と同じ)からなる化合物では、フロテー
シヨン時のインキ捕集性、インキ離脱性に劣る。 オキシアルキレン基を構成するアルキレンオキ
シドとしては、エチレンオキシド、プロピレンオ
キシド、ブチレンオキシド等が挙げられ、2種以
上のアルキレンオキシドを付加しても良い。2種
以上のアルキレンオキシドの付加は、ランダム付
加、もしくはブロツク付加することによつて行う
ことができるが、ランダム付加又はエチレンオキ
シドとエチレンオキシドを除くアルキレンオキシ
ドのブロツク付加が好ましい。 R2はH又は炭素数1〜22のアルキル基、アル
ケニル基ないしはアシル基であるが、H、メチル
基、又は炭素数8〜22のアシル基が好ましい。 また、全分子量が2000以下となることが重要
で、2000を越えるとフロテーシヨン時のインキ捕
集性、発泡性に劣り、高品質の再生パルプが得ら
れない。 次に(b)反応生成物について説明する。 本発明に用いられる天然油脂としては、ヤシ
油、パーム油、オリーブ油、大豆油、菜種油、ア
マニ油等の植物油、豚脂、牛脂、骨油等の動物
油、魚油及びこれらの硬化油、半硬化油、更には
これらの油脂の精製工程で得られる回収油等が挙
げられる。 また多価アルコールとしては、エチレングリコ
ール、プロピレングリコール、トリメチレングリ
コール、ブチレングリコール、グリセリン、トリ
メチロールプロパン、トリメチロールエタン、
1,2,4−ブタントリオール、1,2,6−ヘ
キサントリオール、1,1,1−トリメチロール
ヘキサノール、ペンタエリスリトール、テトラメ
チロールシクロヘキサノール、ジグリセリン等が
挙げられる。 アルキレンオキシドとしては、エチレンオキシ
ド、プロピレンオキシド、ブチレンオキシド等が
挙げられる。アルキレンオキシドの付加は、混合
して付加する(ランダム付加)か、もしくは順次
付加(ブロツク付加)することによつて行うこと
ができるが、ランダム付加又はエチレンオキシド
とエチレンオキシドを除くアルキレンオキシドの
ブロツク付加が好ましい。 天然油脂と多価アルコールの混合割合はモル比
で1:0.1〜1:3、好ましくは1:0.3〜1:2
である。 アルキレンオキシドは天然油脂と多価アルコー
ルの和1モルに対して5モル以上、特に20〜100
モルを使用するのが好ましい。5モル未満である
と古紙からのインキ離脱性、フロテーシヨン処理
時の発泡性が低下する。 天然油脂と多価アルコールとアルキレンオキシ
ドとの反応は、通常は上記の割合で混合した天然
油脂と多価アルコールとの混合物にアルキレンオ
キシドを吹き込み、アルキレンオキシドの付加反
応と共に天然油脂、多価アルコール間のエステル
交換反応を生起させる方法がとられるが、順序を
変えてまず多価アルコールにアルキレンオキシド
を反応させておき、それと天然油脂を反応させる
という方法をとつても、同じ脱墨性能を有する物
が得られる。 付加反応は特に限定されるものではなく、一般
に行われている活性水素を有する化合物へのアル
キレンオキシド付加反応の条件下で行うことがで
きる。例えば、上記モル比で仕込んだ天然油脂と
多価アルコールとの混合物に触媒量のアルカリ性
物質を加え、これに約100〜200℃、1〜3Kg/cm2
でアルキレンオキシドを数時間反応させることに
よつてなし得る。 本発明の脱墨剤において、(a)、(b)の成分の配合
比は、重量比で(a)/(b)=70/30〜5/95の範囲で
あり、好ましくは60〜40〜30/70である。この範
囲を外れるとインキ凝集性、フロテーシヨン時の
発泡性のバランスが崩れるため、高白色度、低残
インキ数のパルプを得ることができない。即ち、
(a)/(b)=70/30より大きくなるとフロテーシヨン
で高泡性となり、パルプの流出が大きく、しかも
インキ凝集性に劣る。また、(a)/(b)=5/95より
小さくなるとフロテーシヨンで低泡性となり、凝
集インキを効率よく系外へ除去することができ
ず、高品質の脱墨パルプを得ることができない。
その結果、上記範囲外では未剥離インキが多量存
在し、低品質の脱墨パルプしか得られない。 本発明の脱墨剤は、古紙離解工程、熟成タワー
工程の何れか、又は両工程へ分割添加しても良い
が、古紙離解工程へ添加した場合が最も効果を発
揮する。 添加量は原料古紙に対して0.2〜1.0重量%が好
ましい。また、本発明の脱墨剤は従来一般に用い
られている公知の脱墨剤と併用することも可能で
ある。 〔実施例及び発明の効果〕 以下、実施例により本発明を具体的に説明する
が、本発明はこれら実施例に限定されるものでは
ない。 実施例 1 まず、表−1に示す組成で本発明の(b)成分(試
料1〜7)を調製した。次いで、市中回収新聞古
紙を2×5cmに細断後、その一定量を卓上離解機
に入れ、その中に水及び苛性ソーダ(対原料)
1.0%(重量基準、以下同じ)、硅酸ソーダ(対原
料)3.0%、30%過酸化水素水(対原料)3.0%、
表−2に示す各種の脱墨剤(対原料)0.4%を加
え、パルプ濃度5%、55℃、20分離解した後、50
℃にて60分間熟成した。その後水を加えてパルプ
濃度を1.0%に稀釈し、CaCl2(対原料)1.0%を添
加し、30℃にて10分間フロテーシヨン処理を施し
た。フロテーシヨン後のパルプスラリーを6%濃
度まで濃縮後、水を加えて1%濃度に稀釈し、
TAPPIシートマシンにてパルプシートを作製し
た。得られたパルプシートを測色色差計にて白色
度を測定し、画像解析装置(×126倍)にて残イ
ンキ数及び未剥離インキ数を測定した。結果を併
せて表−2に示す。
[Industrial Application Field] The present invention relates to a deinking agent used when recycling used paper such as newspapers and magazines. More specifically, when deinking newspapers, magazines, etc. by the flotation method, in order to obtain deinked pulp with high whiteness and a small number of residual inks derived from offset ink, especially deinked pulp with a small number of unpeeled inks. This invention relates to a deinking agent for recycling used paper. [Prior art and problems] Recycling of newspapers, magazines, etc. has been carried out for a long time, but recently it has become especially important, and the use of deinked pulp is also becoming more advanced. Demand is increasing. On the other hand, in recent years, the situation with waste paper has become even more difficult from the perspective of deinking due to changes in printing technology, printing methods, changes in printing ink components, weight reduction, etc., and improvements have also been made to equipment to further promote deinking. are being added. Chemicals traditionally used to separate and remove ink and other impurities from waste paper include alkaline agents such as caustic soda, sodium silicate, and sodium phosphate, and bleaching agents such as hydrogen peroxide, hyposulfite, and hypochlorite. There are metal ion sequestering agents such as DTPA and EDTA, and along with these agents, anionic active agents such as alkylbenzene sulfonates, higher alcohol sulfate ester salts, α-olefin sulfonates, and dialkyl sulfosuccinates are used as deinking agents. agent,
Nonionic surfactants such as higher alcohols, EO adducts of alkylphenols, EO/PO adducts, and alkanolamides have been used singly or in combination of two or more. However, these deinking agents have a low ability to separate and remove ink during flotation treatment, and therefore there has been a demand for the development of a deinking agent that has excellent ink coagulation ability. In addition, it is difficult to completely separate ink from waste paper, and as the use of deinked pulp has expanded and the blending ratio has increased recently, the presence of ink that has not separated from waste paper, that is, unreleased ink, has become a problem. There is a growing demand for the development of deinking agents with even better ink release properties. [Means for Solving the Problems] Therefore, the present inventors have developed a paper that has excellent ink removal power from waste paper, and furthermore, in the flotation process, the released ink is adsorbed to air bubbles and separated and removed from the pulp fibers, resulting in high whiteness and As a result of intensive research to develop a deinking agent that can obtain deinked pulp with a low number of residual inks, especially a deinked pulp with a low number of unreleased inks,
The invention has been completed. That is, the present invention provides (a) a compound represented by general formula (1) R 1 COO−(AO)− o R 2 ...(1) (in formula (1), R 1 is an OH group as a substituent) R2 represents H or an alkyl group, alkenyl group or acyl having 1 to 22 carbon atoms, and AO
represents an oxyalkylene group having 2 to 4 carbon atoms,
n is a number such that the overall molecular weight is 2000 or less. ) and (b) Deinking for used paper recycling, which is made by mixing the reaction products of natural oils and fats, polyhydric alcohols, and alkylene oxides in a weight ratio of (a)/(b) = 70/30 to 5/95. It is intended to provide an agent for The compound represented by the general formula (1) according to the present invention is critical, and even if it is a similar compound, it cannot obtain the remarkable effects of the present invention. I can't do it. Therefore, the limitations and numerical values of the functional groups represented by general formula (1) are extremely important. For example, instead of R 1 COO- group, R 1 O- group (R 1 is a general formula
The same conditions as in (1)) are inferior in ink collection and ink release properties during flotation. Examples of the alkylene oxide constituting the oxyalkylene group include ethylene oxide, propylene oxide, butylene oxide, etc., and two or more types of alkylene oxides may be added. The addition of two or more alkylene oxides can be carried out by random addition or block addition, but random addition or block addition of ethylene oxide and alkylene oxides other than ethylene oxide is preferred. R2 is H or an alkyl group, alkenyl group, or acyl group having 1 to 22 carbon atoms, and preferably H, a methyl group, or an acyl group having 8 to 22 carbon atoms. Furthermore, it is important that the total molecular weight is 2000 or less; if it exceeds 2000, the ink collection and foaming properties during flotation will be poor, making it impossible to obtain high-quality recycled pulp. Next, (b) reaction products will be explained. Natural oils and fats used in the present invention include vegetable oils such as coconut oil, palm oil, olive oil, soybean oil, rapeseed oil, and linseed oil, animal oils such as lard, beef tallow, and bone oil, fish oils, and hydrogenated and semi-hardened oils thereof. Further examples include recovered oils obtained in the refining process of these oils and fats. Polyhydric alcohols include ethylene glycol, propylene glycol, trimethylene glycol, butylene glycol, glycerin, trimethylolpropane, trimethylolethane,
Examples include 1,2,4-butanetriol, 1,2,6-hexanetriol, 1,1,1-trimethylolhexanol, pentaerythritol, tetramethylolcyclohexanol, diglycerin, and the like. Examples of the alkylene oxide include ethylene oxide, propylene oxide, butylene oxide, and the like. The addition of alkylene oxides can be carried out by mixing (random addition) or sequential addition (block addition), but random addition or block addition of ethylene oxide and alkylene oxides other than ethylene oxide is preferred. . The mixing ratio of natural oil and fat and polyhydric alcohol is 1:0.1 to 1:3 in molar ratio, preferably 1:0.3 to 1:2.
It is. Alkylene oxide is 5 mol or more, especially 20 to 100, per 1 mol of the sum of natural oil and fat and polyhydric alcohol.
Preference is given to using moles. If the amount is less than 5 moles, the ink release property from waste paper and the foaming property during flotation treatment will be reduced. The reaction between natural fats, polyhydric alcohols, and alkylene oxides is usually carried out by blowing alkylene oxide into a mixture of natural fats, polyhydric alcohols, and natural oils mixed in the above proportions, and reacting with the addition reaction of the alkylene oxides between the natural fats and polyhydric alcohols. However, even if you change the order and first react the alkylene oxide with the polyhydric alcohol, and then react it with the natural oil, you will not be able to obtain a product that has the same deinking performance. is obtained. The addition reaction is not particularly limited, and can be carried out under the conditions of a commonly used alkylene oxide addition reaction to a compound having active hydrogen. For example, a catalytic amount of an alkaline substance is added to a mixture of natural oils and fats and polyhydric alcohol prepared in the above molar ratio, and the mixture is heated at about 100 to 200°C and 1 to 3 kg/cm 2 .
This can be achieved by reacting an alkylene oxide for several hours. In the deinking agent of the present invention, the blending ratio of components (a) and (b) is in a weight ratio of (a)/(b) = 70/30 to 5/95, preferably 60 to 40. ~30/70. If it is outside this range, the balance between ink cohesiveness and foamability during flotation will be disrupted, making it impossible to obtain pulp with high whiteness and a low number of remaining inks. That is,
If (a)/(b) is greater than 70/30, flotation results in high foaming, pulp outflow is large, and ink cohesion is poor. Furthermore, when (a)/(b) is smaller than 5/95, the flotation results in low foaming, making it impossible to efficiently remove aggregated ink from the system, making it impossible to obtain high-quality deinked pulp.
As a result, outside the above range, a large amount of unpeeled ink is present and only low-quality deinked pulp can be obtained. The deinking agent of the present invention may be added separately to either the waste paper disintegration process, the aging tower process, or both processes, but it is most effective when added to the waste paper disintegration process. The amount added is preferably 0.2 to 1.0% by weight based on the raw waste paper. Further, the deinking agent of the present invention can also be used in combination with known deinking agents that have been commonly used. [Examples and Effects of the Invention] Hereinafter, the present invention will be specifically explained with reference to Examples, but the present invention is not limited to these Examples. Example 1 First, component (b) of the present invention (samples 1 to 7) was prepared with the composition shown in Table 1. Next, after shredding the recycled newspapers into 2 x 5 cm pieces, put a certain amount of them into a tabletop disintegrator, and add water and caustic soda (to the raw material).
1.0% (by weight, same below), sodium silicate (based on raw materials) 3.0%, 30% hydrogen peroxide solution (based on raw materials) 3.0%,
Add 0.4% of various deinking agents (based on raw materials) shown in Table 2, and dissolve at 55℃ for 20 minutes at a pulp concentration of 5%.
Aged for 60 minutes at ℃. Thereafter, water was added to dilute the pulp to 1.0%, 1.0% CaCl 2 (based on raw materials) was added, and a flotation treatment was performed at 30° C. for 10 minutes. After the pulp slurry after flotation was concentrated to a concentration of 6%, water was added to dilute it to a concentration of 1%.
A pulp sheet was produced using a TAPPI sheet machine. The whiteness of the obtained pulp sheet was measured using a colorimeter, and the number of remaining inks and the number of unpeeled inks was measured using an image analyzer (×126 magnification). The results are also shown in Table-2.

【表】【table】

【表】 オキシドである。
[Table] Oxide.

【表】 〓 〓はランダム付加を意味する。
実施例 2 市中回収新聞古紙を2×5cmに細断後、その一
定量を卓上離解機に入れ、その中に水及び苛性ソ
ーダ(対原料)1.0%、硅酸ソーダ3号(対原料)
0.5%、表−3に示す各種の脱墨剤(対原料)0.4
%を加え、パルプ濃度5%、45℃、20分離解後、
パルプ濃度を18%になる様に脱水し、その中に苛
性ソーダ(対原料)1.5%、硅酸ソーダ3号(対
原料)2.5%、30%過酸化水素水(対原料)3.0%
を加えて混合した後、55℃、90分間、パルプ濃度
15%で熟成処理を行つた。その後パルプ濃度4%
になる様に水を加え卓上離解機で5分間離解処理
を施し、更に水を加えてパルプ濃度を1.0%に稀
釈し、CaCl2(対原料)1.0%を添加し、30℃にて
10分間フロテーシヨン処理を行つた。フロテーシ
ヨン後のパルプスラリーを6%濃度まで濃縮後、
水を加えて1%濃度に稀釈し、TAPPIシートマ
シンにてパルプシートを作製した。得られたパル
プシートを測色色差計にて白色度を測定し、画像
解析装置(×126倍)にて残インキ数及び未剥離
インキ数を測定した。結果を併せて表−3に示
す。
[Table] 〓 〓 means random addition.
Example 2 After shredding municipally collected newspaper waste into 2 x 5 cm pieces, put a certain amount of it into a tabletop disintegrator, and add water, caustic soda (based on raw materials) 1.0%, and sodium silicate No. 3 (based on raw materials).
0.5%, various deinking agents shown in Table 3 (based on raw materials) 0.4
%, pulp concentration 5%, 45℃, 20 separations,
Dehydrate the pulp to a concentration of 18%, and add 1.5% caustic soda (based on the raw material), 2.5% sodium silicate No. 3 (based on the raw material), and 3.0% hydrogen peroxide solution (based on the raw material).
After adding and mixing, 55℃, 90 minutes, pulp density
Aging treatment was performed at 15%. Then pulp concentration 4%
Add water and disintegrate for 5 minutes using a tabletop disintegrator, add water to dilute the pulp to 1.0%, add 1.0% CaCl 2 (based on raw materials), and store at 30℃.
Flotation treatment was performed for 10 minutes. After concentrating the pulp slurry after flotation to a concentration of 6%,
The mixture was diluted with water to a concentration of 1%, and a pulp sheet was produced using a TAPPI sheet machine. The whiteness of the obtained pulp sheet was measured using a colorimeter, and the number of remaining inks and the number of unpeeled inks was measured using an image analyzer (×126 magnification). The results are also shown in Table 3.

【表】【table】

Claims (1)

【特許請求の範囲】 1 (a) 一般式(1)で表される化合物 R1COO−(AO)−oR2 ……(1) (式(1)中、R1は置換基としてOH基を有してい
てもよい炭素数7〜21のアルキル基又はアルケ
ニル基、R2はH又は炭素数1〜22のアルキル
基、アルケニル基ないしはアシルを表し、AO
は炭素数2〜4のオキシアルキレン基を表し、
nは全体の分子量が2000以下となる数である。) 及び (b) 天然油脂と多価アルコールとアルキレンオキ
シドとの反応生成物 を重量比で(a)/(b)=70/30〜5/95の割合で混合
してなる古紙再生用脱墨剤。 2 反応生成物が天然油脂と多価アルコールの和
1モルに対して5モル以上のアルキレンオキシド
を付加して得られたものである特許請求の範囲第
1項記載の古紙再生用脱墨剤。 3 天然油脂と多価アルコールとの混合割合が、
モル比で1:0.1〜1:3である特許請求の範囲
第1項記載の古紙再生用脱墨剤。
[Claims] 1 (a) Compound represented by general formula (1) R 1 COO−(AO)− o R 2 ...(1) (In formula (1), R 1 is OH as a substituent) an alkyl group or alkenyl group having 7 to 21 carbon atoms which may have a group, R2 represents H or an alkyl group having 1 to 22 carbon atoms, alkenyl group or acyl, AO
represents an oxyalkylene group having 2 to 4 carbon atoms,
n is a number such that the overall molecular weight is 2000 or less. ) and (b) Deinking for used paper recycling, which is made by mixing the reaction products of natural oils and fats, polyhydric alcohols, and alkylene oxides in a weight ratio of (a)/(b) = 70/30 to 5/95. agent. 2. The deinking agent for waste paper recycling according to claim 1, wherein the reaction product is obtained by adding 5 moles or more of alkylene oxide to 1 mole of the sum of natural oil and fat and polyhydric alcohol. 3 The mixing ratio of natural oil and fat and polyhydric alcohol is
The deinking agent for waste paper recycling according to claim 1, which has a molar ratio of 1:0.1 to 1:3.
JP62265859A 1987-10-21 1987-10-21 Deinking agent for regenerating old paper Granted JPH01111086A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62265859A JPH01111086A (en) 1987-10-21 1987-10-21 Deinking agent for regenerating old paper

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62265859A JPH01111086A (en) 1987-10-21 1987-10-21 Deinking agent for regenerating old paper

Publications (2)

Publication Number Publication Date
JPH01111086A JPH01111086A (en) 1989-04-27
JPH0423036B2 true JPH0423036B2 (en) 1992-04-21

Family

ID=17423076

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62265859A Granted JPH01111086A (en) 1987-10-21 1987-10-21 Deinking agent for regenerating old paper

Country Status (1)

Country Link
JP (1) JPH01111086A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR920702877A (en) * 1990-10-24 1992-10-28 도끼와 후미가즈 Deodorant
KR940007870B1 (en) * 1990-10-24 1994-08-26 가오오 가부시끼가이샤 Deodorant
US5281358A (en) * 1990-10-24 1994-01-25 Kao Corporation Deinking agent

Also Published As

Publication number Publication date
JPH01111086A (en) 1989-04-27

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