CN103396867A - Synthetic cutting fluid and its preparation method - Google Patents
Synthetic cutting fluid and its preparation method Download PDFInfo
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- CN103396867A CN103396867A CN2013102554623A CN201310255462A CN103396867A CN 103396867 A CN103396867 A CN 103396867A CN 2013102554623 A CN2013102554623 A CN 2013102554623A CN 201310255462 A CN201310255462 A CN 201310255462A CN 103396867 A CN103396867 A CN 103396867A
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Abstract
The invention relates to a synthetic cutting fluid and a preparation method thereof. The synthetic cutting fluid is characterized by being made of the following raw materials by weight part: 2-3 of 2-aminoethyl heptadecenyl imidazoline, 1-2 of zinc naphthenate, 4-5 of glycerol, 1-2 of acrylonitrile, 3-4 of polyethylene glycol, 3-4 of Turkey red oil, 2-3 of ethyl acrylate, 1-2 of diphenethyl diphenol polyoxyethylene ether, 3-4 of polyglycerol fatty acid ester, 5-6 of a membrane assistant, and 240 of water. The cutting fluid provided in the invention has the advantages of long service life, environmental protection, and low cost.
Description
Technical field
The invention belongs to the cutting fluid technical field, relate to a kind of synthesis type cutting fluid and preparation method thereof.
Background technology
In mechanical processing industry, be to cut and lubricate with cooling with lubricating oil or with the kerosene apply oil basically.In the course of processing, the oil product waste is very serious, and environment and operator are caused to very large injury; And be difficult to obtain desirable finished surface.And it is slow to add the man-hour radiating rate, after processing work, and very easy upper rust.
Be badly in need of now the design oilness good, rustless property is superior, the cutting fluid that speed of cooling is fast, cleaning performance is good.
Summary of the invention
The purpose of this invention is to provide a kind of synthesis type cutting fluid and preparation method thereof.
The technical solution adopted in the present invention is:
A kind of synthesis type cutting fluid is characterized in that being made by the raw material of following weight part:
2-aminoethyl 17 alkenyl imidazoline 2-3, zinc naphthenate 1-2, glycerine 4-5, vinyl cyanide 1-2, polyoxyethylene glycol 3-4, alizarin assistant 3-4, ethyl propenoate 2-3, hexichol ethyl biphenyl phenol polyethenoxy ether 1-2, polyglycerol fatty acid ester 3-4, film auxiliary agent 5-6, water 240.
Described film auxiliary agent is made by the raw material of following weight part: ricinolic acid 3-4, aluminum nitride powder 1-2,2-amino-2-methyl-1-propyl alcohol 2-3, Silane coupling agent KH550 1-2, vinyl acetate 2-3, fatty alcohol-polyoxyethylene ether 1-2, tertbutyl peroxide 0.2-0.3, morpholine 1-2, ethylene glycol 4-5, tributyl citrate 2-3.
The preparation method is: vinyl acetate, fatty alcohol-polyoxyethylene ether, ethylene glycol, tributyl citrate, ricinolic acid, aluminum nitride powder, 2-amino-2-methyl-1-propyl alcohol are mixed, add tertbutyl peroxide, stirring reaction 2-3 hour, be heated to 130-140 ℃, add again Silane coupling agent KH550 and other remaining component, continue stirring reaction 1-2 hour and get final product.
The preparation method of described synthesis type cutting fluid, it is characterized in that comprising the following steps: glycerine, vinyl cyanide, polyoxyethylene glycol, alizarin assistant, ethyl propenoate are mixed, be heated to 90-105 ℃, stir 80-105 minute, then, add hexichol ethyl biphenyl phenol polyethenoxy ether, polyglycerol fatty acid ester, 2-aminoethyl 17 alkenyl imidazolines to continue to stir 30-40 minute, last, add other remaining component stirred 40-60 minute and get final product.
Cutting fluid of the present invention has long service life, environmental protection, advantage with low cost.The present invention can form protective membrane at workpiece surface; can deposit more than 1 year; oilness, cooling, cleaning, good antirust property; and has rust removing function; the protection cutter, in the work-ing life of prolongation cutter, processing work can not get rusty in 5 days; be conducive to workpiece and enter next procedure, in operating process, can not cause any bad impact to human body and Working environment etc.
Embodiment
A kind of synthesis type cutting fluid, by the raw material of following weight part (kilogram), made:
2-aminoethyl 17 alkenyl imidazolines 3, zinc naphthenate 2, glycerine 5, vinyl cyanide 2, polyoxyethylene glycol 3, alizarin assistant 3, ethyl propenoate 3, hexichol ethyl biphenyl phenol polyethenoxy ether 2, polyglycerol fatty acid ester 3, film auxiliary agent 5, water 240.
Described film auxiliary agent is made by the raw material of following weight part (kilogram): ricinolic acid 4, aluminum nitride powder 2,2-amino-2-methyl-1-propyl alcohol 3, Silane coupling agent KH550 1, vinyl acetate 3, fatty alcohol-polyoxyethylene ether 2, tertbutyl peroxide 0.3, morpholine 2, ethylene glycol 5, tributyl citrate 2.
The preparation method is: vinyl acetate, fatty alcohol-polyoxyethylene ether, ethylene glycol, tributyl citrate, ricinolic acid, aluminum nitride powder, 2-amino-2-methyl-1-propyl alcohol are mixed, add tertbutyl peroxide, stirring reaction 2-3 hour, be heated to 130-140 ℃, add again Silane coupling agent KH550 and other remaining component, continue stirring reaction 1-2 hour and get final product.
The preparation method of synthesis type cutting fluid, comprise the following steps: glycerine, vinyl cyanide, polyoxyethylene glycol, alizarin assistant, ethyl propenoate are mixed, be heated to 90-105 ℃, stir 80-105 minute, then, add hexichol ethyl biphenyl phenol polyethenoxy ether, polyglycerol fatty acid ester, 2-aminoethyl 17 alkenyl imidazolines to continue to stir 30-40 minute, last, add other remaining component stirred 40-60 minute and get final product.
Utilizing the present invention to carry out steel disc rust prevention test (55 ± 2 ℃) soaks entirely: 30 with the corrosion-free phenomenon of going up to the sky.
Claims (2)
1. synthesis type cutting fluid is characterized in that being made by the raw material of following weight part:
2-aminoethyl 17 alkenyl imidazoline 2-3, zinc naphthenate 1-2, glycerine 4-5, vinyl cyanide 1-2, polyoxyethylene glycol 3-4, alizarin assistant 3-4, ethyl propenoate 2-3, hexichol ethyl biphenyl phenol polyethenoxy ether 1-2, polyglycerol fatty acid ester 3-4, film auxiliary agent 5-6, water 240;
Described film auxiliary agent is made by the raw material of following weight part: ricinolic acid 3-4, aluminum nitride powder 1-2,2-amino-2-methyl-1-propyl alcohol 2-3, Silane coupling agent KH550 1-2, vinyl acetate 2-3, fatty alcohol-polyoxyethylene ether 1-2, tertbutyl peroxide 0.2-0.3, morpholine 1-2, ethylene glycol 4-5, tributyl citrate 2-3;
The preparation method is: vinyl acetate, fatty alcohol-polyoxyethylene ether, ethylene glycol, tributyl citrate, ricinolic acid, aluminum nitride powder, 2-amino-2-methyl-1-propyl alcohol are mixed, add tertbutyl peroxide, stirring reaction 2-3 hour, be heated to 130-140 ℃, add again Silane coupling agent KH550 and other remaining component, continue stirring reaction 1-2 hour and get final product.
2. the preparation method of synthesis type cutting fluid according to claim 1 is characterized in that comprising the following steps:
Glycerine, vinyl cyanide, polyoxyethylene glycol, alizarin assistant, ethyl propenoate are mixed, be heated to 90-105 ℃, stir 80-105 minute, then, add hexichol ethyl biphenyl phenol polyethenoxy ether, polyglycerol fatty acid ester, 2-aminoethyl 17 alkenyl imidazolines to continue to stir 30-40 minute, finally, add other remaining component stirred 40-60 minute and get final product.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2013102554623A CN103396867A (en) | 2013-06-25 | 2013-06-25 | Synthetic cutting fluid and its preparation method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
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| CN2013102554623A CN103396867A (en) | 2013-06-25 | 2013-06-25 | Synthetic cutting fluid and its preparation method |
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| CN103396867A true CN103396867A (en) | 2013-11-20 |
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| CN2013102554623A Pending CN103396867A (en) | 2013-06-25 | 2013-06-25 | Synthetic cutting fluid and its preparation method |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103981007A (en) * | 2014-04-21 | 2014-08-13 | 苏州捷德瑞精密机械有限公司 | Antirust transparent cutting fluid and preparation method thereof |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002053882A (en) * | 2000-08-04 | 2002-02-19 | Samitto Corporation:Kk | Slurry composition for cutting brittle material and method for cutting using the same |
| CN101531946A (en) * | 2009-04-22 | 2009-09-16 | 上海应用技术学院 | Metal cutting solution of green semi-synthesis double-base oil and preparation method thereof |
| WO2012166615A1 (en) * | 2011-05-27 | 2012-12-06 | Howard University | Hybrid nanolubricant |
-
2013
- 2013-06-25 CN CN2013102554623A patent/CN103396867A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002053882A (en) * | 2000-08-04 | 2002-02-19 | Samitto Corporation:Kk | Slurry composition for cutting brittle material and method for cutting using the same |
| CN101531946A (en) * | 2009-04-22 | 2009-09-16 | 上海应用技术学院 | Metal cutting solution of green semi-synthesis double-base oil and preparation method thereof |
| WO2012166615A1 (en) * | 2011-05-27 | 2012-12-06 | Howard University | Hybrid nanolubricant |
Non-Patent Citations (1)
| Title |
|---|
| 周雍鑫，周俊: "《金属加工液使用指南》", 31 May 2000, 中国石化出版社，机械工业出版社 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103981007A (en) * | 2014-04-21 | 2014-08-13 | 苏州捷德瑞精密机械有限公司 | Antirust transparent cutting fluid and preparation method thereof |
| CN103981007B (en) * | 2014-04-21 | 2016-07-06 | 苏州捷德瑞精密机械有限公司 | A kind of anti-rust transparent cutting liquid and preparation method thereof |
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Application publication date: 20131120 |
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