JPS6121513B2 - - Google Patents

Info

Publication number
JPS6121513B2
JPS6121513B2 JP10711879A JP10711879A JPS6121513B2 JP S6121513 B2 JPS6121513 B2 JP S6121513B2 JP 10711879 A JP10711879 A JP 10711879A JP 10711879 A JP10711879 A JP 10711879A JP S6121513 B2 JPS6121513 B2 JP S6121513B2
Authority
JP
Japan
Prior art keywords
present
addition
properties
rust prevention
grinding
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
Application number
JP10711879A
Other languages
Japanese (ja)
Other versions
JPS5632593A (en
Inventor
Tomoo Kainuma
Ryoji Kaneda
Takashi Tokue
Yoshinori Hayakawa
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 KAGAKU KOGYO KK
Original Assignee
TOHO KAGAKU KOGYO KK
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 KAGAKU KOGYO KK filed Critical TOHO KAGAKU KOGYO KK
Priority to JP10711879A priority Critical patent/JPS5632593A/en
Publication of JPS5632593A publication Critical patent/JPS5632593A/en
Publication of JPS6121513B2 publication Critical patent/JPS6121513B2/ja
Granted legal-status Critical Current

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  • Lubricants (AREA)

Description

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

本発明は鉄鋼、機械工業等の金属加工における
研削作業に使用する研削剤に関するもので下記一
般式 〔但し、R1,R2,R3は水素原子もしくは炭素
数3〜4のアルキル基(但しR1,R2,R3が同時
に水素原子であることはない。)nは1及び2の
整数、XはNa,K1等の金属原子NH4基及びアミ
ン中和N−アンモニウム基を示す。〕 にて表わされるアルキルフエノキシアルキレンカ
ルボン酸塩(以下本発明の化合物という)を含有
することを特徴とする新規で優れた研削剤に関す
るものである。 一般に研削剤として要求される性能としては、
潤滑作用により発熱したものを冷却し、仕上面の
精度を高め、砥石の目つぶれや目こぼれを防止
し、砥石寿命を延長し、更に金属に対する研削
性、加工金属の防錆性及び防腐性を向上すると共
に使用液の消泡性等が良好で非鉄金属への影響が
なく、廃液処理が良好である等々の条件が要求さ
れる。 従来、研削剤としては亜硝酸塩が主に使用され
ている。亜硝酸塩は、研削性、防錆性、消泡性
等々については良好であるが最近の発表によると
発生したニトロソアミンによる発癌性の問題や廃
液処理が困難という欠点がある。また亜硝酸塩に
代つて縮合リン酸塩、ホウ酸塩、合成脂肪酸等が
使用されているが、これらも防錆性、防腐性、消
泡性及び臭気等の問題があり、研削業界から上記
の如き要請に対して、充分満足されるものではな
かつた。 本発明者等は研削剤として上述の条件を満す化
合物について研究の結果本発明の化合物を見い出
し、本発明に至つたものである。本発明の研究の
過程で硅酸塩、縮合リン酸塩、ホウ酸塩等の無機
化合物及びリン酸エステル塩、多塩基酸塩、植物
油脂系脂肪酸塩、合成脂肪酸塩等の有機化合物に
ついて研削剤としての性能(防錆性、消泡性)を
評価したが、殆んどのものが防錆性が弱く、また
泡立ち易く、使用に耐えるものがなかつた。ただ
合成カルボン酸系統中、本発明において用いる化
合物、アルキルフエノキシアルキレンカルボン酸
塩が研削性、防錆性、消泡性に優れ研削剤として
使用可能であることがわかつた。本発明は、これ
らの知見に基づいて完成されたものであり、アル
キルフエノキシアルキレンカルボン酸塩を含有す
ることを特徴とする研削剤である。本発明の主化
合物は通常アルキルフエノールのフエノラートに
モノハロゲンアルキレンカルボン酸塩を反応させ
るなどの公知の方法によつて容易に得ることが出
来る。 用いるアルキルフエノールとしては、プロピル
フエノール、イソプロピルフエノール、ジイソプ
ロピルフエノール、トリプロピルフエノール、ブ
チルフエノール、ジブチルフエノール等々があ
る。 本発明の目的からは、炭素数4のブチルフエノ
ールが最も好ましくアルキル基の炭素数が大きく
なるに従い発泡が大きくなり且つ研削性も低下す
る。 モノハロゲンアルキレンカルボン酸塩として使
用出来るものは、モノクロロ酢酸、モノクロロプ
ロピオン酸、モノプロム酢酸等があるが、本発明
の目的と経済性からモノクロロ酢酸を用いること
が好ましい。 一般式における塩の生成に用いる化合物として
は苛性ソーダ、苛性カリ及び水酸化リチウム等の
水溶液及びアンモニア水等の無機のアルカリがあ
るが、その他アミン付加塩があり、それらのもの
として、炭素数6以下のアルカノールアミン、炭
素数4以下のアルキル基を有するアルキルアミン
及びそのアルキルアルカノールアミン、環状アミ
ン、ポリアルキレンポリアミン等がある。経済的
には、苛性ソーダ、苛性カリ、アルカノールアミ
ンを用いるのが好ましい。 本発明の主体は研削剤としてアルキルフエノキ
シアルキレンカルボン酸塩を用いることにあるが
迸ばれたアミン付加塩を用いることにより一層効
果が向上することがある。 本発明に用いる化合物は通常0.1〜20%濃度の
効果を発揮するが、更に好ましい濃度は0.3〜1.0
%の範囲である。本発明の化合物の濃度が0.1%
以下になると防錆性が低下し、20%以上になると
研削性、消泡性等の性能が低下する傾向にあり好
ましくない。 本発明の研削剤に種々の加工に適合した性能を
持たせるために、界面活性剤と防腐剤等を適量添
加し調整できることは云うまでもない。 以下、従来使用されている亜硝酸塩、P−ター
シヤリーブチル安息香酸塩と本発明の化合物を用
いた場合との効果の比較実施例を挙げ、本発明を
具体的に説明しその性能が優れていることを示
す。 実施例 1
The present invention relates to an abrasive used for grinding work in metal processing in steel, machinery, etc. [However, R 1 , R 2 , and R 3 are hydrogen atoms or alkyl groups having 3 to 4 carbon atoms (However, R 1 , R 2 , and R 3 are never hydrogen atoms at the same time.) n is 1 and 2. The integer X represents a metal atom NH 4 group such as Na or K 1 and an amine-neutralized N-ammonium group. ] The present invention relates to a novel and excellent abrasive characterized by containing an alkylphenoxyalkylene carboxylic acid salt represented by (hereinafter referred to as the compound of the present invention). The performance generally required for an abrasive is as follows:
The lubrication action cools the heat generated, improves the precision of the finished surface, prevents the grinding wheel from becoming crushed or spilled, extends the life of the grinding wheel, and further improves the grindability of metals and the rust prevention and corrosion resistance of processed metals. Conditions are required, such as improved defoaming properties of the liquid used, no impact on non-ferrous metals, and good waste liquid treatment. Conventionally, nitrites have been mainly used as abrasives. Nitrite has good properties in terms of grindability, rust prevention, antifoaming properties, etc., but according to recent publications, it has drawbacks such as carcinogenicity due to generated nitrosamines and difficulty in waste liquid treatment. In addition, condensed phosphates, borates, synthetic fatty acids, etc. are used in place of nitrites, but these also have problems such as rust prevention, antiseptic properties, antifoaming properties, and odor, and the grinding industry Such requests were not fully satisfied. The present inventors have discovered the compound of the present invention as a result of research into compounds that meet the above-mentioned conditions as abrasives, and have arrived at the present invention. In the course of the research of the present invention, inorganic compounds such as silicates, condensed phosphates, and borates, and organic compounds such as phosphate ester salts, polybasic acid salts, vegetable oil-based fatty acid salts, and synthetic fatty acid salts were used as abrasives. We evaluated their performance (rust prevention and antifoaming properties), but most of them had poor rust prevention and foamed easily, so none were usable. However, among the synthetic carboxylic acid series, the compound used in the present invention, the alkylphenoxyalkylene carboxylate, has been found to have excellent grinding properties, rust prevention properties, and antifoaming properties and can be used as an abrasive. The present invention was completed based on these findings, and is a grinding agent characterized by containing an alkylphenoxyalkylene carboxylate. The main compound of the present invention can be easily obtained by a known method such as reacting a phenolate of an alkylphenol with a monohalogen alkylene carboxylate. Examples of the alkylphenol used include propylphenol, isopropylphenol, diisopropylphenol, tripropylphenol, butylphenol, dibutylphenol, and the like. For the purposes of the present invention, butylphenol having 4 carbon atoms is most preferred, as the larger the number of carbon atoms in the alkyl group, the greater the foaming and the lower the grindability. Examples of monohalogen alkylene carboxylic acid salts that can be used include monochloroacetic acid, monochloropropionic acid, and monopromoacetic acid, but it is preferable to use monochloroacetic acid from the viewpoint of the purpose of the present invention and economic efficiency. Compounds used to generate salts in the general formula include aqueous solutions such as caustic soda, caustic potash, and lithium hydroxide, and inorganic alkalis such as aqueous ammonia, but there are also amine addition salts. Examples include alkanolamines, alkylamines having an alkyl group having 4 or less carbon atoms, alkylalkanolamines thereof, cyclic amines, polyalkylene polyamines, and the like. From an economic standpoint, it is preferable to use caustic soda, caustic potash, or alkanolamine. Although the main feature of the present invention is to use an alkylphenoxyalkylene carboxylate as an abrasive, the effect may be further improved by using a sputtered amine addition salt. The compound used in the present invention usually exhibits an effect at a concentration of 0.1 to 20%, but a more preferable concentration is 0.3 to 1.0%.
% range. The concentration of the compound of the invention is 0.1%
If it is less than 20%, the rust prevention property will decrease, and if it is more than 20%, performance such as grindability and antifoaming property will tend to decrease, which is not preferable. It goes without saying that in order to give the abrasive of the present invention properties suitable for various processing, suitable amounts of surfactants, preservatives, etc. can be added and adjusted. Hereinafter, the present invention will be specifically explained by comparing the effects of conventionally used nitrite, P-tert-butylbenzoate, and the compound of the present invention, and its performance will be demonstrated. Indicates that there is a Example 1

【表】 上記試料の各混合割合は50%ずつとして調整し
た。 実施例 2
[Table] The mixing ratio of each of the above samples was adjusted to 50%. Example 2

【表】 測定条件; 研削盤 円筒研削盤 砥 石 WA60K 回転数 1500r.p.m 被削剤 SCR22 切り込み 1.5μ/rev.【table】 Measurement condition; Grinding machine Cylindrical grinding machine Whetstone WA60K Rotation speed 1500r.p.m Work material SCR22 Depth of cut 1.5μ/rev.

【表】 条 件; 研削盤 ロール研削盤 砥 石 ダイヤモンド砥石 被削材 S45C 切り込み 5/1000mm 実施例 3【table】 Condition; Grinding machine Roll grinding machine Whetstone Diamond whetstone Work material S45C Depth of cut 5/1000mm Example 3

【表】 以下実施例4〜7における比較例、実施例に用
いた化合物は、それぞれ50%づつ配合調整したも
のである。 実施例 4
[Table] The compounds used in the comparative examples and examples in Examples 4 to 7 below were adjusted by 50% each. Example 4

【表】 円筒容器に試料液2採取し、流量10/min
の循環量で液面より62cmの高さから流下させ循環
させる。その時の泡高を測定した。 実施例 5
[Table] Collect 2 sample solutions in a cylindrical container, flow rate 10/min
It is circulated by flowing it down from a height of 62cm above the liquid level with a circulation rate of . The foam height at that time was measured. Example 5

【表】 実施例 6【table】 Example 6

【表】 予じめ滅菌した綿付き三角フラスコに試料液を
滅菌水7/1000に希釈した液を50ml作成する。これ
に菌液を1ml添加し、35〜37℃で次のインターバ
ルで菌の測定を行つた。
[Table] Prepare 50 ml of the sample solution diluted with 7/1000 sterile water in a pre-sterilized Erlenmeyer flask with cotton. 1 ml of bacterial solution was added to this, and the bacteria were measured at 35-37°C at the following intervals.

【表】 添 測添 測添 添 測添 添 測
加 定加 定加 加 定加 加 定
尚菌液はブイヨン培地にソルブルタイプの腐敗
液を白金線で添加し35〜37℃で24時間培養した。
(菌数109〜10の菌数を使用) A;生菌数(個/ml)102以下 B 〃 102〜103 C 〃 103〜104 D 〃 104〜105 E 〃 105以上 実施例 7
[Table] Addition Measurement Addition Measurement Addition Addition Measurement Addition Measurement Addition Addition Addition Addition Addition Addition Addition Addition Measurement Addition Measurement Addition Measurement Addition Measurement Addition Addition Addition Addition Addition For the bacterial solution, add soluble type rotting liquid to the bouillon medium using a platinum wire and culture at 35 to 37℃ for 24 hours. did.
(Use a bacterial count of 10 9 to 10 ) A; Number of viable bacteria (cells/ml) 10 2 or less B 10 2 to 10 3 C 10 3 to 10 4 D 10 4 to 10 5 E 10 5 or more examples 7

【表】 塩化第二鉄でPHを4以下にし、石灰を中和(PH
7〜8)し、高分子凝集剤でブロツクを形成させ
た後ろ過する。ろ液をJIS K−0102,−13,−16に
準じて測定した。
[Table] Lower the pH to 4 or less with ferric chloride and neutralize lime (PH
7-8), form a block with a polymer flocculant, and then filter. The filtrate was measured according to JIS K-0102, -13, -16.

Claims (1)

【特許請求の範囲】 1 下記一般式 〔但しR1,R2,R3は水素原子もしくは炭素数
3〜4のアルキル基(但しR1,R2,R3が同時に
水素原子である事はない。)nは1及び2の整
数、XはNa,K,NH4基、アミン中和N−アン
モニウム基を示す〕で表されるアルキルフエノキ
シアルキレンカルボン酸塩を含有する事を特徴と
する水溶性研削剤。
[Claims] 1. The following general formula [However, R 1 , R 2 , and R 3 are hydrogen atoms or alkyl groups having 3 to 4 carbon atoms (However, R 1 , R 2 , and R 3 are never hydrogen atoms at the same time.) n is an integer of 1 and 2. , X represents Na, K, NH 4 group, or amine-neutralized N-ammonium group.
JP10711879A 1979-08-24 1979-08-24 Grinding agent Granted JPS5632593A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10711879A JPS5632593A (en) 1979-08-24 1979-08-24 Grinding agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10711879A JPS5632593A (en) 1979-08-24 1979-08-24 Grinding agent

Publications (2)

Publication Number Publication Date
JPS5632593A JPS5632593A (en) 1981-04-02
JPS6121513B2 true JPS6121513B2 (en) 1986-05-27

Family

ID=14450930

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10711879A Granted JPS5632593A (en) 1979-08-24 1979-08-24 Grinding agent

Country Status (1)

Country Link
JP (1) JPS5632593A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63117099A (en) * 1986-11-05 1988-05-21 Idemitsu Kosan Co Ltd Additive for emulsion-type lubricant
JPS63117096A (en) * 1986-11-05 1988-05-21 Idemitsu Kosan Co Ltd Water-soluble additive

Also Published As

Publication number Publication date
JPS5632593A (en) 1981-04-02

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