CN102465053A - Environment-friendly cutting solution - Google Patents

Environment-friendly cutting solution Download PDF

Info

Publication number
CN102465053A
CN102465053A CN2010105516352A CN201010551635A CN102465053A CN 102465053 A CN102465053 A CN 102465053A CN 2010105516352 A CN2010105516352 A CN 2010105516352A CN 201010551635 A CN201010551635 A CN 201010551635A CN 102465053 A CN102465053 A CN 102465053A
Authority
CN
China
Prior art keywords
cutting fluid
additive
ester
back flow
flow reaction
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.)
Granted
Application number
CN2010105516352A
Other languages
Chinese (zh)
Other versions
CN102465053B (en
Inventor
胡丽天
秦宝锋
冯大鹏
张永胜
曾继华
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.)
Lanzhou Institute of Chemical Physics LICP of CAS
Original Assignee
Lanzhou Institute of Chemical Physics LICP of CAS
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 Lanzhou Institute of Chemical Physics LICP of CAS filed Critical Lanzhou Institute of Chemical Physics LICP of CAS
Priority to CN 201010551635 priority Critical patent/CN102465053B/en
Publication of CN102465053A publication Critical patent/CN102465053A/en
Application granted granted Critical
Publication of CN102465053B publication Critical patent/CN102465053B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Lubricants (AREA)

Abstract

The invention discloses an environment-friendly cutting solution. The cutting solution comprises the following ingredients: polyethyleneglycol, silicone emulsion, disodium ethylene diamine tetraacetate, trolamine, additives and distilled water. The cutting solution is free from containing toxic chemicals producing unfavorable influence on the human body or the environment such as nitrite, organic phenol and the like, and has characteristics such as rust resistance, abrasion resistance and high lubrication.

Description

Environmental Protection Cutting Fluid
Technical field
The present invention relates to a kind of environmental type cutting fluid.
Background technology
Metal cutting processing is the most common, most widely used a kind of in the metal processing.Cutting fluid is the important supplementary material of metal cutting processing.The purpose of using metal working fluid is exactly the friction that reduces between cutting force and cutter and the workpiece; The heat of in time taking away generation in the cutting zone reduces tool wear to reduce cutting temperature, improves tool life; Thereby enhance productivity; Improve workpiece surface roughness, guarantee the workpiece working accuracy, reach economic optimum.Therefore, using cutting fluid is to improve processing quality and the important measures that cut down finished cost.
Cutting fluid has cooling, lubricated, cleaning and antirust four kinds of major functions.In recent years, because the improving constantly of cutting technology, the continuing to bring out of advanced cutting machine, the development of cutter and workpiece material has promoted the update of cutting fluid kind, also requires cutting fluid to have following function: 1. erosion resistance.2. anti-putridness.3. water quality flexibility.4. paint flexibility.5. stable.6. security and the hypotoxicity 8. defoaming that 7. has no irritating odor.9. emission treatment is easy.10. liquid waste disposal is easy.Especially environment in recent years protection and human health become the focus of whole society's concern day by day, and cutting fluid can pollute and damage environment and human body, so the use of cutting fluid and liquid waste disposal have received the restriction of environmental regulation increasingly stringent.Traditional aspects such as oil base cutting fluid rust-preventing characteristic, stability, cooling property and environmental protection obviously lag behind the development of modern Machining Technology for Cutting, begin the water-base cutting fluid development to nuisanceless or low public hazards.
In developed country, microemulsion generally uses, and is studying Environmental Protection Cutting Fluid energetically.Domestic also good to performance, that the life-span is long synthetic cutting fluid, microemulsion transition from emulsion.At present, the key content of cutting fluid research both at home and abroad comprises: the development of high-performance cutting fluid, the feed liquid method that prolongs cutting fluid work-ing life and the research of minimizing discharging of waste liquid amount, more effective and more economical method for treating waste liquid research etc.And be the important directions of cutting fluid research to ecotope and the human health spinoff is little, processing characteristics is superior cutting fluid.The emphasis of research and development is at present: MO is replaced by biological degradation good vegetables oil and synthetic ester gradually; The oil base cutting fluid is replaced by water-base cutting fluid gradually; Exploitation excellent property and harmless and additive environmentally safe.
Summary of the invention
The object of the present invention is to provide a kind of Environmental Protection Cutting Fluid.
A kind of Environmental Protection Cutting Fluid is characterized in that this cutting fluid prepares through following method:
Synthesizing of A additive: get the mixing in 1: 1 in molar ratio of fatty ester and Hydrazine Hydrate 80 and be dissolved in the ethanol, back flow reaction 12~48 hours is cooled to below 20 ℃, and suction filtration with absolute ethanol washing, suction filtration, gets white solid; White solid and anhydride compound were dissolved in chloroform or the ETHYLE ACETATE back flow reaction 0.5~3 hour in 1: 1 in molar ratio; Add trolamine again in 1: 1 in molar ratio~1: 3, continued back flow reaction 0.5~2 hour, boil off solvent, obtain additive;
The preparation of B cutting fluid: the weight percentage of each component of cutting fluid is polyoxyethylene glycol 5~15%, silicone emulsion 0.25~1.0%, EDTA Disodium 0.1~1.0%, trolamine 1~10%, additive 1~10%, distilled water surplus; Regulate pH value to 7.5~9 with alkaline matter and process Environmental Protection Cutting Fluid.
Synthetic additive of the present invention is faint yellow solid or viscous liquid to reddish-brown, and is water-soluble.It is a kind of tensio-active agent, has wear-resistant simultaneously and characteristics high lubricity.
In the building-up process of additive, fatty ester is fatty acid methyl ester, ethyl ester, positive butyl ester or other the fatty ester that contains 6~18 carbon atoms that contains 6~18 carbon atoms.
In the building-up process of additive, anhydride compound is Succinic anhydried or MALEIC ANHYDRIDE or Citric anhydride.
Described molecular weight polyethylene glycol is 400~2000, and polyoxyethylene glycol can make that each component is dispersed in the water better in the cutting fluid, strengthens the lubricity of cutting fluid simultaneously.
Described EDTA Disodium can form the water soluble complex of stabilizer pole with metals ion.
Described trolamine is a kind of water miscible rust-preventive agent, and effectively the protective money metal surface is prevented oxidation.
Cutting fluid of the present invention does not contain noxious chemicals such as the nitrite that human body or environment are had a negative impact, organic phenol, has the characteristics of antirust, wear-resistant and high lubricity.
Embodiment
For a better understanding of the present invention, describe through embodiment.
Embodiment 1
In the 500mL flask with three necks,round bottom of reflux condensing tube and TM is housed, add 220g n butyl oleate, 21g 85% Hydrazine Hydrate 80 and 250mL ethanol, refluxed 48 hours, be cooled to suction filtration below 20 ℃, with absolute ethanol washing, suction filtration, get white solid.
In the 250mL flask with three necks,round bottom of reflux condensing tube and TM is housed, 30g oleoyl hydrazine, 10g Succinic anhydried and 50mL ETHYLE ACETATE, reflux was reacted 1 hour.Add trolamine 30g, continued back flow reaction 1 hour, boil off solvent ethyl acetate, get faint yellow solid.
With polyoxyethylene glycol 8g, silicone emulsion 0.5g, EDTA Disodium 0.5g, trolamine 5g and appeal synthetic additive 3g are dissolved in an amount of zero(ppm) water, and using aqueous sodium hydroxide solution to regulate the pH value again is 8, obtains the cutting fluid that total amount is 100g.
Embodiment 2
In the 500mL flask with three necks,round bottom of reflux condensing tube and TM is housed, add 220g n butyl oleate, 21g 85% Hydrazine Hydrate 80 and 250mL ethanol, refluxed 48 hours, be cooled to suction filtration below 20 ℃, with absolute ethanol washing, suction filtration, get white solid.
In the 250mL flask with three necks,round bottom of reflux condensing tube and TM is housed, 30g oleoyl hydrazine, 10g MALEIC ANHYDRIDE and 50mL ETHYLE ACETATE, reflux was reacted 1 hour.Add trolamine 30g, continued back flow reaction 1 hour, boil off solvent ethyl acetate, get faint yellow solid.
With polyoxyethylene glycol 12g, silicone emulsion 0.6g, EDTA Disodium 0.6g, trolamine 6g and above-mentioned synthetic additive 4g are dissolved in an amount of zero(ppm) water, and using aqueous sodium hydroxide solution to regulate the pH value again is 9, obtains the cutting fluid that total amount is 100g.
Embodiment 3
In the 500mL flask with three necks,round bottom of reflux condensing tube and TM is housed, add 150g Laurate ethyl, 21g 85% Hydrazine Hydrate 80 and 250mL ethanol, refluxed 24 hours, be cooled to suction filtration below 20 ℃, with absolute ethanol washing, suction filtration, get the white plates crystal.
In the 250mL flask with three necks,round bottom of reflux condensing tube and TM is housed, 21.4g LAURIC ACID 99 MIN hydrazides, 10g MALEIC ANHYDRIDE and 50mL ETHYLE ACETATE, reflux was reacted 1 hour.Add trolamine 30g, continued back flow reaction 1 hour, boil off solvent ethyl acetate, get faint yellow solid.
With polyoxyethylene glycol 10g, silicone emulsion 0.4g, EDTA Disodium 0.5g, trolamine 7g and above-mentioned synthetic additive 4g are dissolved in an amount of zero(ppm) water, and using aqueous sodium hydroxide solution to regulate the pH value again is 7.5, obtains the cutting fluid that total amount is 100g.
Embodiment 4
In the 500mL flask with three necks,round bottom of reflux condensing tube and TM is housed, add 150g Laurate ethyl, 21g 85% Hydrazine Hydrate 80 and 250mL ethanol, refluxed 24 hours, be cooled to suction filtration below 20 ℃, with absolute ethanol washing, suction filtration, get the white plates crystal.
In the 250mL flask with three necks,round bottom of reflux condensing tube and TM is housed, 21.4g LAURIC ACID 99 MIN hydrazides, 10g Succinic anhydried and 50mL ETHYLE ACETATE, reflux was reacted 1 hour.Add trolamine 30g, continued back flow reaction 1 hour, boil off solvent ethyl acetate, get faint yellow solid.
With polyoxyethylene glycol 7g, silicone emulsion 0.5g, EDTA Disodium 0.7g, trolamine 10g and above-mentioned synthetic additive 4g are dissolved in an amount of zero(ppm) water, and using aqueous sodium hydroxide solution to regulate the pH value again is 8, obtains the cutting fluid that total amount is 100g.
Embodiment 5
In the 500mL flask with three necks,round bottom of reflux condensing tube and TM is housed, add 150g Laurate ethyl, 21g 85% Hydrazine Hydrate 80 and 250mL ethanol, refluxed 24 hours, be cooled to suction filtration below 20 ℃, with absolute ethanol washing, suction filtration, get the white plates crystal.
In the 250mL flask with three necks,round bottom of reflux condensing tube and TM is housed, 21.4g LAURIC ACID 99 MIN hydrazides, 17.4g Citric anhydride and 50mL ETHYLE ACETATE, reflux was reacted 1 hour.Add trolamine 60g, continued back flow reaction 1 hour, boil off solvent ethyl acetate, get faint yellow solid.
With polyoxyethylene glycol 12g, silicone emulsion 0.4g, EDTA Disodium 0.7g, trolamine 10g and appeal synthetic additive 5g are dissolved in an amount of zero(ppm) water, and using aqueous sodium hydroxide solution to regulate the pH value again is 8, obtains the cutting fluid that total amount is 100g.
The performance comparison experiment: the cutting fluid of embodiment 1 preparation and the cutting ability of zero(ppm) water have been carried out contrast test, and the result sees table 1
The performance of fully synthetic cutting fluid relatively

Claims (4)

1. Environmental Protection Cutting Fluid is characterized in that this cutting fluid prepares through following method:
Synthesizing of A additive: get the mixing in 1: 1 in molar ratio of fatty ester and Hydrazine Hydrate 80 and be dissolved in the ethanol, back flow reaction 12~48 hours is cooled to below 20 ℃, and suction filtration with absolute ethanol washing, suction filtration, gets white solid; White solid and anhydride compound were dissolved in chloroform or the ETHYLE ACETATE back flow reaction 0.5~3 hour in 1: 1 in molar ratio; Add trolamine again in 1: 1 in molar ratio~1: 3, continued back flow reaction 0.5~2 hour, boil off solvent, obtain additive;
The preparation of B cutting fluid: the weight percentage of each component of cutting fluid is polyoxyethylene glycol 5~15%, silicone emulsion 0.25~1.0%, EDTA Disodium 0.1~1.0%, trolamine 1~10%, additive 1~10%, distilled water surplus; Regulate pH value to 7.5~9 with alkaline matter and process Environmental Protection Cutting Fluid.
2. cutting fluid as claimed in claim 1 is characterized in that fatty ester is fatty acid methyl ester, ethyl ester, positive butyl ester or other the fatty ester that contains 6~18 carbon atoms that contains 6~18 carbon atoms.
3. cutting fluid as claimed in claim 1 is characterized in that anhydride compound is Succinic anhydried or MALEIC ANHYDRIDE or Citric anhydride.
4. cutting fluid as claimed in claim 1 is characterized in that molecular weight polyethylene glycol is 400~2000.
CN 201010551635 2010-11-16 2010-11-16 Environment-friendly cutting solution Active CN102465053B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 201010551635 CN102465053B (en) 2010-11-16 2010-11-16 Environment-friendly cutting solution

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 201010551635 CN102465053B (en) 2010-11-16 2010-11-16 Environment-friendly cutting solution

Publications (2)

Publication Number Publication Date
CN102465053A true CN102465053A (en) 2012-05-23
CN102465053B CN102465053B (en) 2013-10-16

Family

ID=46069180

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 201010551635 Active CN102465053B (en) 2010-11-16 2010-11-16 Environment-friendly cutting solution

Country Status (1)

Country Link
CN (1) CN102465053B (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102839043A (en) * 2012-10-09 2012-12-26 天津利纳斯化工有限公司 Cutting fluid complexing agent and preparation method thereof
CN104263477A (en) * 2014-09-25 2015-01-07 无锡康柏斯机械科技有限公司 Emulsified metal cutting fluid and preparation method thereof
CN104946371A (en) * 2015-05-26 2015-09-30 安徽不二越精工轴承有限公司 Environment-friendly cutting fluid
CN106995743A (en) * 2017-04-29 2017-08-01 无锡赛晶太阳能有限公司 A kind of silicon wafer cutting fluid
CN111747864A (en) * 2020-07-27 2020-10-09 中国科学院兰州化学物理研究所 Preparation method of water-based cutting fluid additive with good solubility

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1046752A (en) * 1989-08-24 1990-11-07 黄龙安 The method of a kind of processing multiple-effect type synthetic cutting fluid (DS-8901 type synthetic cutting fluid)
KR20060104572A (en) * 2005-03-31 2006-10-09 주식회사 비아이티범우연구소 Aqueous cutting oil composite
CN101161797A (en) * 2007-09-28 2008-04-16 北京东兴润滑剂有限公司 Water-soluble discharging medium compound for electrospark wire-electrode cutting
CN101265434A (en) * 2008-04-23 2008-09-17 常州市夏雷化学有限公司 Water-soluble cutting liquid for super-fine honing

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1046752A (en) * 1989-08-24 1990-11-07 黄龙安 The method of a kind of processing multiple-effect type synthetic cutting fluid (DS-8901 type synthetic cutting fluid)
KR20060104572A (en) * 2005-03-31 2006-10-09 주식회사 비아이티범우연구소 Aqueous cutting oil composite
CN101161797A (en) * 2007-09-28 2008-04-16 北京东兴润滑剂有限公司 Water-soluble discharging medium compound for electrospark wire-electrode cutting
CN101265434A (en) * 2008-04-23 2008-09-17 常州市夏雷化学有限公司 Water-soluble cutting liquid for super-fine honing

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102839043A (en) * 2012-10-09 2012-12-26 天津利纳斯化工有限公司 Cutting fluid complexing agent and preparation method thereof
CN104263477A (en) * 2014-09-25 2015-01-07 无锡康柏斯机械科技有限公司 Emulsified metal cutting fluid and preparation method thereof
CN104946371A (en) * 2015-05-26 2015-09-30 安徽不二越精工轴承有限公司 Environment-friendly cutting fluid
CN106995743A (en) * 2017-04-29 2017-08-01 无锡赛晶太阳能有限公司 A kind of silicon wafer cutting fluid
CN111747864A (en) * 2020-07-27 2020-10-09 中国科学院兰州化学物理研究所 Preparation method of water-based cutting fluid additive with good solubility

Also Published As

Publication number Publication date
CN102465053B (en) 2013-10-16

Similar Documents

Publication Publication Date Title
CN104498164B (en) A kind of environmentally-friendly water-based magnesium alloy cutting fluid of anticorrosive Anti- tarnishing
CN101323813A (en) Multiple-effect type water-based synthesized cutting solution and preparation thereof
CN100485018C (en) Rust-proof cutting fluid
CN105482888A (en) Complete synthesis cutting fluid capable of meeting machining requirements of multiple materials
CN102311864B (en) Cutting fluid special for NC machine tools
CN102465053B (en) Environment-friendly cutting solution
CN102703196B (en) Environment-friendly water-based metal cutting fluid
CN104277902A (en) Heavy-load metal machining total synthesis cutting fluid as well as preparation method and application thereof
CN104164283A (en) Microemulsion metal cutting fluid
CN105176656A (en) Environment-friendly semisynthetic cutting fluid for titanium alloys as well as preparation method and application of cutting fluid
CN1746281A (en) Environmental-protective water-base synthesized cutting fluid
CN102559352A (en) Self-emulsified total synthesis cutting solution
CN108048197B (en) Fully-synthetic cutting fluid suitable for aluminum alloy processing and preparation method thereof
CN104479833A (en) High-efficiency safe environment-friendly all-synthetic cutting fluid and preparation method thereof
CN105524688A (en) Extreme pressure cutting oil used for achieving performance stability in metal processing and preparation method thereof
CN107541328B (en) Emission-free recyclable water-based cutting fluid and preparation method thereof
CN106635369A (en) Fully synthetic cutting fluid and production method thereof
CN108003994A (en) A kind of environment-friendly type extreme pressure cutting oil and its preparation method and application
CN105296131A (en) Chlorine-sulfur-phosphor-less high-extreme pressure fully synthetic cutting fluid and preparation method thereof
CN104593129A (en) Total-synthesis water-base metal cutting fluid and preparation method
CN102899154A (en) Fully synthetic cutting solution
CN105695050A (en) Metal cutting fluid
CN104312705B (en) A kind of environment-friendlycutting cutting fluid and preparation method thereof
CN102746932B (en) A kind of preparation method of environment protection water-based metal working fluid
CN107253945A (en) BTA imidazolidine derivatives and its preparation method and application

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant