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
Links
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 description 10
- 238000005259 measurement Methods 0.000 description 9
- -1 ferrous metals Chemical class 0.000 description 7
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 7
- 230000002265 prevention Effects 0.000 description 7
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000003254 anti-foaming effect Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 239000003082 abrasive agent Substances 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 150000007942 carboxylates Chemical class 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 2
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000001642 boronic acid derivatives Chemical class 0.000 description 2
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 150000002826 nitrites Chemical class 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 235000011118 potassium hydroxide Nutrition 0.000 description 2
- 239000012488 sample solution Substances 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- GAWAYYRQGQZKCR-REOHCLBHSA-N (S)-2-chloropropanoic acid Chemical compound C[C@H](Cl)C(O)=O GAWAYYRQGQZKCR-REOHCLBHSA-N 0.000 description 1
- TZIPJVAKPHGVFU-UHFFFAOYSA-N 2,3,4-tripropylphenol Chemical compound CCCC1=CC=C(O)C(CCC)=C1CCC TZIPJVAKPHGVFU-UHFFFAOYSA-N 0.000 description 1
- NSENZNPLAVRFMJ-UHFFFAOYSA-N 2,3-dibutylphenol Chemical compound CCCCC1=CC=CC(O)=C1CCCC NSENZNPLAVRFMJ-UHFFFAOYSA-N 0.000 description 1
- CRBJBYGJVIBWIY-UHFFFAOYSA-N 2-isopropylphenol Chemical compound CC(C)C1=CC=CC=C1O CRBJBYGJVIBWIY-UHFFFAOYSA-N 0.000 description 1
- LCHYEKKJCUJAKN-UHFFFAOYSA-N 2-propylphenol Chemical compound CCCC1=CC=CC=C1O LCHYEKKJCUJAKN-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 101100008049 Caenorhabditis elegans cut-5 gene Proteins 0.000 description 1
- 206010007269 Carcinogenicity Diseases 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001734 carboxylic acid salts Chemical class 0.000 description 1
- 230000007670 carcinogenicity Effects 0.000 description 1
- 231100000260 carcinogenicity Toxicity 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000004005 nitrosamines Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 1
- 229940031826 phenolate Drugs 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- OLBCVFGFOZPWHH-UHFFFAOYSA-N propofol Chemical compound CC(C)C1=CC=CC(C(C)C)=C1O OLBCVFGFOZPWHH-UHFFFAOYSA-N 0.000 description 1
- 102200082816 rs34868397 Human genes 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000008223 sterile water Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Lubricants (AREA)
Description
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)
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.
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)
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 |
-
1979
- 1979-08-24 JP JP10711879A patent/JPS5632593A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5632593A (en) | 1981-04-02 |
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