Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JP5649376B2 - Defoamer for kraft pulp manufacturing process - Google Patents
[go: Go Back, main page]

JP5649376B2 - Defoamer for kraft pulp manufacturing process - Google Patents

Defoamer for kraft pulp manufacturing process Download PDF

Info

Publication number
JP5649376B2
JP5649376B2 JP2010193951A JP2010193951A JP5649376B2 JP 5649376 B2 JP5649376 B2 JP 5649376B2 JP 2010193951 A JP2010193951 A JP 2010193951A JP 2010193951 A JP2010193951 A JP 2010193951A JP 5649376 B2 JP5649376 B2 JP 5649376B2
Authority
JP
Japan
Prior art keywords
group
kraft pulp
manufacturing process
antifoaming agent
pulp manufacturing
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.)
Active
Application number
JP2010193951A
Other languages
Japanese (ja)
Other versions
JP2012052246A (en
Inventor
啓介 野田
啓介 野田
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.)
Toho Chemical Industry Co Ltd
Original Assignee
Toho Chemical Industry Co Ltd
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 Toho Chemical Industry Co Ltd filed Critical Toho Chemical Industry Co Ltd
Priority to JP2010193951A priority Critical patent/JP5649376B2/en
Publication of JP2012052246A publication Critical patent/JP2012052246A/en
Application granted granted Critical
Publication of JP5649376B2 publication Critical patent/JP5649376B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Degasification And Air Bubble Elimination (AREA)
  • Detergent Compositions (AREA)
  • Polyethers (AREA)
  • Paper (AREA)

Description

本発明はクラフトパルプ製造工程における消泡剤に関する。   The present invention relates to an antifoaming agent in a kraft pulp manufacturing process.

従来、クラフトパルプ製造工程において発泡抑制のため消泡剤が多量に使用されている。特に現在は、倉敷料削減のため保管チップの減少によるシーズニング不足により、クラフトパルプ製造工程での発泡が問題となっている。また、近年広葉樹をパルプ化する際、アカシア材を配合するケースが増加している。アカシア材はこれまで使用されてきたユーカリ材と比較し、樹脂量が多く、且つ樹脂のアルキル鎖長が長いことが知られている。このため、クラフトパルプ製造工程において高温高アルカリ条件化で樹脂が加水分解され、発泡性分である脂肪酸石鹸が多量に発生するばかりではなく、長鎖脂肪酸石鹸の影響で硬く消えづらい泡が発生する。現在、広葉樹のクラフトパルプ製造工程でアカシア材が高配合されている場合、現在使用されている消泡剤では、使用量が増加し、製造原単位の増加、更には抄造工程でピッチトラブルが多発する傾向が見られる。特にアカシア材を5%配合しただけで、消泡剤使用量、抄造工程でのピッチ発生量が倍増した工場もある。   Conventionally, a large amount of an antifoaming agent has been used to suppress foaming in the kraft pulp manufacturing process. In particular, foaming in the kraft pulp manufacturing process has become a problem due to lack of seasoning due to a decrease in storage chips in order to reduce Kurashiki materials. In recent years, cases of blending acacia wood are increasing when pulping hardwood. It is known that an acacia material has a larger amount of resin and a longer alkyl chain length than the eucalyptus material that has been used so far. For this reason, in the kraft pulp manufacturing process, the resin is hydrolyzed under high-temperature and high-alkaline conditions, and not only a large amount of fatty acid soap, which is a foaming component, is generated, but also foam that is hard and hard to disappear is generated due to the influence of long-chain fatty acid soap. . Currently, when acacia wood is highly blended in the hardwood kraft pulp manufacturing process, the amount of defoaming agent currently used increases, the production unit increases, and pitch trouble occurs frequently in the papermaking process. The tendency to do is seen. Some factories have doubled the amount of defoamer used and the amount of pitch generated in the papermaking process, especially by blending 5% acacia wood.

クラフトパルプ製造工程用消泡剤として、特許文献1ではポリオキシアルキレン化合物が使用されているが、エチレンオキサイドの含有率が高く、黒液に対する安定性や消泡試験での即効性はあるものの、2分以上での抑泡効果(持続性)に劣る。また、シリコーンを配合することにより即効性を向上させており、界面活性剤単独としての効果は劣る。
工場実機でも界面活性剤系消泡剤を使用するケースはこれまで確認されていない。
As a defoaming agent for kraft pulp manufacturing process, a polyoxyalkylene compound is used in Patent Document 1, but the content of ethylene oxide is high, and although there is an immediate effect in the stability and defoaming test against black liquor, It is inferior in the foam suppression effect (sustainability) in 2 minutes or more. Moreover, the immediate effect is improved by mix | blending silicone, and the effect as surfactant independent is inferior.
No case of using a surfactant-based antifoaming agent has been confirmed in actual factories.

特開平11−276806号公報JP-A-11-276806

本発明が解決しようとする課題は、広葉樹パルプ製造時、アカシア材が配合されたクラフトパルプ製造工程での発泡トラブルを回避でき、更には黒液中の脂肪酸、樹脂酸やリグニン等の有機物の凝集物発生量を抑制できる消泡剤に関するものである。   The problem to be solved by the present invention is that during hardwood pulp production, it is possible to avoid foaming troubles in the kraft pulp production process in which acacia materials are blended, and further aggregation of fatty acids in black liquor, organic acids such as resin acids and lignin The present invention relates to an antifoaming agent capable of suppressing the amount of generated matter.

本発明者らは、前記課題を解決するために鋭意検討を重ねた結果、特定のアルキレンオキサイド付加物からなる消泡剤が上記課題を解決できることを見出し、本発明を完成するに至った。すなわち本発明は、下記一般式(1)で表される、グリフィンのHLBが1〜6のアルキレンオキサイド付加物を含有するクラフトパルプ製造工程用消泡剤に関するものである。

O(AO)H (1)

(式中、Rは炭素数8〜22のアルキル基、アルケニル基、または炭素数6〜30のアリール基を示し、AOは炭素数2〜4のアルキレンオキシ基、nは1〜100の整数を示す。)
As a result of intensive studies in order to solve the above problems, the present inventors have found that an antifoaming agent comprising a specific alkylene oxide adduct can solve the above problems, and have completed the present invention. That is, this invention relates to the antifoamer for kraft pulp manufacturing processes containing the alkylene oxide adduct whose HLB of griffin is 1-6 represented by following General formula (1).

R 1 O (AO) n H (1)

(In the formula, R 1 represents an alkyl group having 8 to 22 carbon atoms, an alkenyl group, or an aryl group having 6 to 30 carbon atoms, AO represents an alkyleneoxy group having 2 to 4 carbon atoms, and n represents an integer of 1 to 100. Is shown.)

本発明により、クラフトパルプ製造工程で優れた消泡効果を発揮する消泡剤を提供できる。また、本発明の消泡剤は、黒液中の脂肪酸、樹脂酸やリグニン等の有機物の凝集物発生量を抑制することが可能となる。   The present invention can provide an antifoaming agent that exhibits an excellent antifoaming effect in the kraft pulp manufacturing process. In addition, the antifoaming agent of the present invention can suppress the amount of aggregates of organic substances such as fatty acids, resin acids and lignin in the black liquor.

以下に、本発明のクラフトパルプ製造工程用消泡剤について詳述する。
前記一般式(1)において、Rは炭素数8〜22のアルキル基、アルケニル基、または炭素数6〜30のアリール基であるが、好ましくは炭素数14〜18のアルキル基またはアルケニル基である。炭素数8〜22のアルキル基、アルケニル基は直鎖、分岐のいずれであってもよく、また環状構造を有するものであってもよい。
Below, the antifoamer for kraft pulp manufacturing process of this invention is explained in full detail.
In the general formula (1), R 1 is an alkyl group having 8 to 22 carbon atoms, an alkenyl group, or an aryl group having 6 to 30 carbon atoms, preferably an alkyl group or alkenyl group having 14 to 18 carbon atoms. is there. The alkyl group and alkenyl group having 8 to 22 carbon atoms may be linear or branched, and may have a cyclic structure.

前記一般式(1)において、AOは炭素数2〜4のアルキレンオキシ基を表し、具体的にはエチレンオキシ基、プロピレンオキシ基およびブチレンオキシ基が挙げられる。nはアルキレンオキシ基の繰り返し数を表し、1〜100の整数であるが、20〜50の範囲が好ましい。nが2以上の場合繰り返し単位中にはエチレンオキシ基が必ず1以上存在することを必須とし、プロピレンオキシ基やブチレンオキシ基を有する場合にはそれらのいずれか一種のみを有していてもよいし双方有していてもよい。2種以上のアルキレンオキシ基を有する場合はランダム状に付加していてもブロック状に付加していてもよい。   In the general formula (1), AO represents an alkyleneoxy group having 2 to 4 carbon atoms, and specific examples include an ethyleneoxy group, a propyleneoxy group, and a butyleneoxy group. n represents the repeating number of the alkyleneoxy group, and is an integer of 1 to 100, but a range of 20 to 50 is preferable. When n is 2 or more, it is essential that at least one ethyleneoxy group is present in the repeating unit, and when it has a propyleneoxy group or a butyleneoxy group, it may have only one of them. And you may have both. When it has two or more types of alkyleneoxy groups, they may be added randomly or in a block form.

本発明に係るアルキレンオキサイド付加物は、一価アルコールや一価フェノールにアルキレンオキサイドを付加することにより合成することができる。一価アルコールとしては、オクチルアルコール、デシルアルコール、ラウリルアルコール、トリデシルアルコール、ミリスチルアルコール、パルミチルアルコール、ステアリルアルコール、オレイルアルコール、ベヘニルアルコール、アルキルシクロヘキサノール等の炭素数8〜22の直鎖、分岐又は環状アルコール等が挙げられる。一価フェノールとしては、モノ・ジ・トリスチレン化フェノール、モノ・ジ・トリベンジルフェノール、オクチルフェノール、ノニルフェノール、ジノニルフェノールやカシューナッツ由来のアルケニルフェノール(カルダノール)が挙げられる。これらは1種または2種以上を用いることができる。   The alkylene oxide adduct according to the present invention can be synthesized by adding alkylene oxide to a monohydric alcohol or monohydric phenol. Examples of monohydric alcohols include octyl alcohol, decyl alcohol, lauryl alcohol, tridecyl alcohol, myristyl alcohol, palmityl alcohol, stearyl alcohol, oleyl alcohol, behenyl alcohol, alkylcyclohexanol, etc. A cyclic alcohol etc. are mentioned. Examples of the monohydric phenol include mono-di-tristyrenated phenol, mono-di-tribenzylphenol, octylphenol, nonylphenol, dinonylphenol, and cashew nut-derived alkenylphenol (cardanol). These can use 1 type (s) or 2 or more types.

本発明に係るアルキレンオキサイド付加物はエチレンオキシ基を親水基、プロピレンオキシ基並びにブチレンオキシ基を疎水基とした場合、グリフィンのHLBで1〜6となるようにアルキレンオキシ基を調整することが望ましく、更に好ましくは2〜5であることが望ましい。HLBが6を超えると黒液中の有機物の分散効果は高まるが、消泡効果が無くなり、逆に発泡の要因となる。また、HLBが1を下回ると、消泡剤自体が凝集してしまい、消泡効果が全く得られなくなる。   In the alkylene oxide adduct according to the present invention, when the ethyleneoxy group is a hydrophilic group, the propyleneoxy group and the butyleneoxy group are hydrophobic groups, it is desirable to adjust the alkyleneoxy group so that the HLB of Griffin is 1 to 6. More preferably, it is 2-5. If the HLB exceeds 6, the dispersion effect of the organic matter in the black liquor is enhanced, but the defoaming effect is lost, and conversely, it causes foaming. On the other hand, if the HLB is less than 1, the antifoaming agent itself aggregates and no defoaming effect can be obtained.

アルキレンオキシ基の付加形態により、消泡効果の発現時期を調整することができる。例えば、一価アルコールや一価フェノール等にエチレンオキサイドを付加した後にプロピレンオキサイドを付加した場合、持続性(抑泡効果)が得られ、逆にプロピレンオキサイドを付加した後にエチレンオキサイドを付加した場合は即効性(破泡効果)が得られる。一方ランダムに付加した場合は、即効性と持続性両方を併せ持つ消泡剤が得られる。   The expression time of the defoaming effect can be adjusted by the addition form of the alkyleneoxy group. For example, when propylene oxide is added after adding ethylene oxide to monohydric alcohol, monohydric phenol, etc., sustainability (foam suppression effect) is obtained, and conversely when ethylene oxide is added after adding propylene oxide Immediate effect (bubble breaking effect) is obtained. On the other hand, when added randomly, an antifoaming agent having both immediate effect and sustainability can be obtained.

本発明の消泡剤に含有される式(1)で表されるアルキレンオキサイド付加物はどのような方法で製造されたものであってもよい。通常は、水酸基に塩基性触媒下アルキレンオキサイドを付加する方法で得ることができる。   The alkylene oxide adduct represented by the formula (1) contained in the antifoaming agent of the present invention may be produced by any method. Usually, it can obtain by the method of adding an alkylene oxide to a hydroxyl group under a basic catalyst.

本発明の消泡剤は製品化の際に水、界面活性剤系乳化剤、水溶性有機溶剤等を配合し、使用してもなんら問題はない。   The antifoaming agent of the present invention has no problem even if it is mixed with water, a surfactant-based emulsifier, a water-soluble organic solvent and the like when it is commercialized.

本発明の消泡剤を使用することにより、広葉樹のクラフトパルプ製造工程で優れた効果を発揮するが、特にアカシア材が5%以上配合された場合に特筆すべき消泡効果が得られる。   By using the antifoaming agent of the present invention, an excellent effect is exhibited in the manufacturing process of hardwood kraft pulp. However, particularly when 5% or more of acacia wood is blended, a defoaming effect to be noted is obtained.

本発明の消泡剤の添加場所は特に限定されないが、クラフトパルプ製造工程において、ブロータンク、ヤンソンスクリーン、精選スクリーン、洗浄機、濾液タンク、若しくは各工程に設置されているポンプのサクション口で添加することが望ましい。本発明の消泡剤の添加量は、工程の発泡状態に左右されるが、通常パルプに対し1〜100ppm、好ましくは2〜50ppmである。また、クラフトパルプ製造工程には他薬剤として、蒸解助剤、ピッチコントロール剤、洗浄剤等が添加されていてもよい。また、鉱物油系消泡剤やシリコーン系消泡剤を補助的に使用しても問題ない。   The place of addition of the antifoaming agent of the present invention is not particularly limited, but in the kraft pulp manufacturing process, it is added at the suction port of a blow tank, Jansson screen, a selective screen, a washing machine, a filtrate tank, or a pump installed in each process. It is desirable to do. Although the addition amount of the antifoamer of this invention is influenced by the foaming state of a process, it is 1-100 ppm normally with respect to a pulp, Preferably it is 2-50 ppm. Moreover, a cooking aid, a pitch control agent, a cleaning agent, etc. may be added to the kraft pulp manufacturing process as other chemicals. Further, there is no problem even if a mineral oil-based antifoaming agent or a silicone-based antifoaming agent is used as an auxiliary.

以下、本発明の実施例を示すが、本発明はこの実施例に限定されるものではない。   Examples of the present invention will be described below, but the present invention is not limited to these examples.

製造例1
温度計、撹拌装置を備えたSUS製オートクレーブにステアリルアルコール81g(0.3モル)、96%苛性カリ1.5gを仕込み、窒素雰囲気下で155±5℃を保ちながらエチレンオキサイド66g(1.5モル)を徐々に導入した後、1時間熟成した。その後、135℃に冷却し、同温度を保ちながらプロピレンオキサイド435g(7.5モル)を徐々に導入した。同温度で3時間熟成した後、酢酸1.7gで触媒の苛性カリを中和した。
本反応により水酸基価29mgKOH/gの参考例の消泡剤No.1の化合物を得た。
Production Example 1
A SUS autoclave equipped with a thermometer and a stirrer was charged with 81 g (0.3 mol) of stearyl alcohol and 1.5 g of 96% caustic potash, and 66 g (1.5 mol) of ethylene oxide while maintaining 155 ± 5 ° C. in a nitrogen atmosphere. ) Was gradually introduced, followed by aging for 1 hour. Thereafter, the mixture was cooled to 135 ° C., and 435 g (7.5 mol) of propylene oxide was gradually introduced while maintaining the same temperature. After aging for 3 hours at the same temperature, the caustic potash of the catalyst was neutralized with 1.7 g of acetic acid.
With this reaction, the antifoaming agent No. 1 in the reference example having a hydroxyl value of 29 mgKOH / g was used. 1 compound was obtained.

以下同様の方法で表1に示す本発明の消泡剤No.4〜6,10〜12,16〜26と、参考例の消泡剤No.2,3,7〜9,13〜15を得た。
表1中のアルキレンオキサイド付加物の−(ハイフン)はブロック付加を、/(スラッシュ)はランダム付加を示す。
In the same manner, the antifoaming agent No. 1 of the present invention shown in Table 1 is used . 4 to 6, 10 to 12, 16 to 26, and antifoam No. 2, 3, 7-9 , 13-15 were obtained.
In Table 1,-(hyphen) in the alkylene oxide adduct indicates block addition, and / (slash) indicates random addition.

Figure 0005649376
Figure 0005649376

上記消泡剤との比較を行うために表2に示される消泡剤を試験に供した。   In order to make a comparison with the antifoaming agent, the antifoaming agents shown in Table 2 were used for the test.

Figure 0005649376
Figure 0005649376

性能評価試験(循環試験)
図1のような装置を用い、黒液に対する消泡効果を確認した。
Performance evaluation test (circulation test)
Using an apparatus as shown in FIG. 1, the defoaming effect on the black liquor was confirmed.

試験方法
図1の循環試験機に黒液1Lを加え80℃に調整後、水流ポンプで黒液を循環させ、泡高さ150mmに達した時点で消泡剤(10ppm)を添加する(流量10L/分)。消泡剤添加後、30秒後、1分後、5分後並びに10分後の泡高さ(mm)を測定した。
Test method 1L of black liquor was added to the circulation tester in Fig. 1 and adjusted to 80 ° C. Then, the black liquor was circulated with a water pump and defoaming agent (10ppm) was added when the foam height reached 150mm (flow rate 10L) / Min). After the addition of the antifoaming agent, the foam height (mm) after 30 seconds, 1 minute, 5 minutes and 10 minutes was measured.

性能評価試験1(広葉樹黒液;アカシア材7%配合)
製紙会社より広葉樹蒸解抽出液を入手(黒液濃度20%)。本抽出液をイオン交換水で5%に希釈し、評価用発泡液とした。
Performance evaluation test 1 (hardwood black liquor; 7% acacia wood)
Obtain hardwood digestion extract from paper company (black liquor concentration 20%). This extract was diluted to 5% with ion-exchanged water to obtain a foaming solution for evaluation.

性能評価試験2(広葉樹黒液;アカシア材50%配合)
製紙会社より広葉樹蒸解抽出液を入手(黒液濃度22%)。本抽出液をイオン交換水で5%に希釈し、評価用発泡液とした。
Performance evaluation test 2 (Hardwood black liquor; 50% acacia mix)
Obtain hardwood digestion extract from paper company (black liquor concentration 22%). This extract was diluted to 5% with ion-exchanged water to obtain a foaming solution for evaluation.

性能評価試験3(消泡剤の黒液に対する分散性)
300mlガラス製ビーカーに80℃に調整した性能評価試験1及び2で使用した黒液を200ml採り、消泡剤を加え1時間撹拌する。その後、100メッシュナイロン布で濾過。凝集物を濾別し、80℃の温水300mlで洗浄、乾燥後、重量を測定し、下記式に従って凝集率を算出した。
Performance evaluation test 3 (dispersibility of antifoaming agent in black liquor)
200 ml of black liquor used in performance evaluation tests 1 and 2 adjusted to 80 ° C. in a 300 ml glass beaker is added, and an antifoaming agent is added and stirred for 1 hour. Then, filter with 100 mesh nylon cloth. The aggregate was separated by filtration, washed with 300 ml of warm water at 80 ° C., dried, weighed, and the aggregation rate was calculated according to the following formula.

Figure 0005649376
Figure 0005649376

Figure 0005649376
Figure 0005649376

Figure 0005649376
Figure 0005649376

Figure 0005649376
Figure 0005649376

消泡効果の試験に供される循環試験機を示す図である。It is a figure which shows the circulation test machine with which the test of a defoaming effect is provided.

1 ガラス製シリンダ
2 流路
3 水流ポンプ
4 コック(廃液時開放)
5 流路
6 バット
7 加温器(IHヒーター)
8 水流ポンプ
1 Glass cylinder 2 Flow path 3 Water pump 4 Cock (Open when waste liquid)
5 Channel 6 Butt 7 Heater (IH heater)
8 Water pump

Claims (1)

下記一般式(1)で表される、エチレンオキシ基を親水基、プロピレンオキシ基並びにブチレンオキシ基を疎水基とした場合のグリフィンのHLBが3.64.7のアルキレンオキサイド付加物を含有するアカシア材が配合されたクラフトパルプ製造工程用消泡剤。
O(AO)H (1)
(式中、Rは炭素数8〜22のアルキル基、アルケニル基、または炭素数6〜30のアリール基を示し、AOは炭素数2〜4のアルキレンオキシ基、nは3050の整数を示す。)
Contains an alkylene oxide adduct represented by the following general formula (1) having an HLB of 3.6 to 4.7 when Griffin has a hydrophilic group, a propyleneoxy group, and a butyleneoxy group as a hydrophobic group. A defoamer for kraft pulp manufacturing process that contains Acacia wood .
R 1 O (AO) n H (1)
(In the formula, R 1 represents an alkyl group having 8 to 22 carbon atoms, an alkenyl group, or an aryl group having 6 to 30 carbon atoms, AO represents an alkyleneoxy group having 2 to 4 carbon atoms, and n represents an integer of 30 to 50 . Is shown.)
JP2010193951A 2010-08-31 2010-08-31 Defoamer for kraft pulp manufacturing process Active JP5649376B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2010193951A JP5649376B2 (en) 2010-08-31 2010-08-31 Defoamer for kraft pulp manufacturing process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2010193951A JP5649376B2 (en) 2010-08-31 2010-08-31 Defoamer for kraft pulp manufacturing process

Publications (2)

Publication Number Publication Date
JP2012052246A JP2012052246A (en) 2012-03-15
JP5649376B2 true JP5649376B2 (en) 2015-01-07

Family

ID=45905872

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010193951A Active JP5649376B2 (en) 2010-08-31 2010-08-31 Defoamer for kraft pulp manufacturing process

Country Status (1)

Country Link
JP (1) JP5649376B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6627040B2 (en) * 2014-06-27 2020-01-08 サンノプコ株式会社 Defoamer
CN107537185B (en) * 2017-08-18 2021-01-15 佳化化学(茂名)有限公司 Self-emulsifying defoaming agent and preparation method thereof
WO2022138870A1 (en) * 2020-12-24 2022-06-30 大王製紙株式会社 Pulp sheet for fluff pulp
CN119034274B (en) * 2024-09-25 2025-11-28 亚太森博(山东)浆纸有限公司 Oil-based defoamer for pulping black liquor, and manufacturing method and application thereof

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58149399A (en) * 1982-02-25 1983-09-05 三菱油化株式会社 Defoaming of papermaking pulp stock liquid or papermaking waste liquor
JPH11199291A (en) * 1998-01-14 1999-07-27 Sannopuko Kk Defoaming agent, building material board and its production
JP5519203B2 (en) * 2009-07-21 2014-06-11 ライオン株式会社 Manufacturing method of kraft pulp

Also Published As

Publication number Publication date
JP2012052246A (en) 2012-03-15

Similar Documents

Publication Publication Date Title
CN101939481B (en) Detergent for kraft pulp and process for producing kraft pulp with the same
US7619043B2 (en) Anti-foam compositions
KR101437427B1 (en) Antifoam compositions
EP3764821B1 (en) Foam control
JP5649376B2 (en) Defoamer for kraft pulp manufacturing process
US9631320B2 (en) Anti-foaming agent and pulp production method
CN110960892A (en) Efficient water-based paint defoaming agent and preparation method thereof
CN1430691A (en) Foam control composition and method for controlling foam in aqueous systems
CN107537185A (en) A kind of self-emulsifying type defoamer and preparation method thereof
US8563640B2 (en) Method for deaerating liquids
JP5519203B2 (en) Manufacturing method of kraft pulp
CN111031809A (en) Foam Control in Food
JP3945278B2 (en) Antifoam composition
CN113797595A (en) A kind of silicone emulsion defoamer and preparation method thereof
JP3668792B2 (en) Defoamer for kraft pulp manufacturing process
JP2001020191A (en) Antifoaming agent for pulp manufacturing process and pulp manufacturing method
JP4562159B2 (en) How to dehydrate lime mud
SE456252B (en) METHOD TO REDUCE THE QUANTITY OF FOAM CREATED IN A PROCESS OF WASHING TYPE FOR DEVICATION OF SECOND FIBER
JP2023552954A (en) Foam control agent for paper and pulp
KR100298138B1 (en) Foam inhibitor composition
KR100790434B1 (en) Antifoam Composition
JP2009185399A (en) Method for inhibiting foaming of unbleached washing filtrate

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20130410

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20140115

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20140121

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20140320

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20140326

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20140422

Free format text: JAPANESE INTERMEDIATE CODE: A821

Effective date: 20140422

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20141111

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20141111

R150 Certificate of patent or registration of utility model

Ref document number: 5649376

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250