CN1317061C - Chelated surfacant - Google Patents
Chelated surfacant Download PDFInfo
- Publication number
- CN1317061C CN1317061C CNB200510016660XA CN200510016660A CN1317061C CN 1317061 C CN1317061 C CN 1317061C CN B200510016660X A CNB200510016660X A CN B200510016660XA CN 200510016660 A CN200510016660 A CN 200510016660A CN 1317061 C CN1317061 C CN 1317061C
- Authority
- CN
- China
- Prior art keywords
- surface active
- active agent
- chelating
- strong
- surfactant
- 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 - Fee Related
Links
Abstract
The present invention relates to a chelating surface active agent which belongs to the technical field of fine chemical industry. The chemical structural formula of the chelating surface active agent is the right formula, wherein X2=O, R2=H, X1=O or N, and R1=an aliphatic radical; X1=O, R1=H, X2=O or N, and R2=an aliphatic radical. The surface active agent simultaneously has strong surface activity and strong chelating capability; when the surface active agent is matched with other surface active agents, the salt resistance and the hard water resistance of a mixing system can be obviously enhanced.
Description
Technical field:
The invention belongs to the fine chemical technology field, relate to a kind of surfactant.
Background technology:
Chelate surfactant, claim chelate surfactant again, wherein studying more is EDTA derivative class surfactant, but its production technology more complicated, use the cyanide of severe toxicity in most production processes again, and the degradability of EDTA itself is being under suspicion recently again.
Summary of the invention:
The technical problem to be solved in the present invention is to disclose a kind of degradable chelate surfactant.
Chelate surfactant provided by the invention is reacted in the presence of catalyst by imino-diacetic butanedioic acid and fatty alcohol or fatty amine and obtains.
Iminobisuccinate derivative class surfactant structure general formula of the present invention is:
X wherein
2=O, R
2=H, X
1=O or N, R
1=aliphatic group;
Perhaps X wherein
1=O, R
1=H, X
2=O or N, R
2=aliphatic group.The aliphatic group carbon atom quantity can be 1 to 30 carbon.
The degradable chelate surfactant that the present invention produces is realized by following steps:
Imino-diacetic butanedioic acid and fatty alcohol or fatty amine can directly react in the presence of catalyst, and this reaction is a reversible reaction, by constantly distilling out or carry out the water that reaction generates, molecular balance are moved to the direction that generates product, improve product yield.This catalyst for reaction is the strong acid compound, adopts sulfuric acid, sulfonic acid etc. usually, and recent development trend is to adopt zeolite molecular sieve, heteropoly acid, solid super-strong acid or strong-acid ion exchange resin, and relevant monograph is more.
Iminobisuccinate derivative class surfactant provided by the invention is a kind of novel surfactant, and chelate surfactant has very strong surface-active and sequestering power simultaneously; During with other surfactant compatibilities, can obviously improve the salt tolerance and the anti-hard water of mixed system; Be suitable for preparing without phosphorus, hyperconcetration heavy-dirty liquid-detergent; Under acid condition, can reduce the corrosion rate of steel, under alkali condition, can make the steel surface passivation and play a protective role, therefore have broad application prospects.And production equipment is simple, and condition control is easy, and technological process is short.
The specific embodiment:
1, synthetic imino-diacetic butanedioic acid single lauryl alcohol ester
Adopt a whole set of Soxhlet extraction element as reaction unit.600 milliliters of dry imino-diacetic butanedioic acid 24.9 grams (0.1 mole), laruyl alcohol 18.6 grams (0.1 mole), 0.5 milliliter in sulfuric acid and solvent dimethyl formamides are housed in the flask.Restrain with filter paper barreled anhydrous magnesium sulfate 100 in the extractor, with the water of taking out of in the absorption reaction system.Agitating heating back flow reaction 15 hours stops.Mixture in the flask is carried out decompression distillation, reclaim most of solvent, about 480 milliliters of dimethyl formamides, residue cooling is poured in 1 liter the cold water, generates precipitation, the agitator treating sediment filters collecting precipitation, and sediment is poured in 1 liter 0.01 mole the sodium bicarbonate solution, agitator treating, filter, wash sediment again with water, sediment is dry under vacuum, 40-50 ℃ condition, obtain product, yield 76%.
2, synthetic imino-diacetic mono succinate acyl lauryl amine
Method of operating is the same, but replaces laruyl alcohol, product yield 79% with 18.5 gram (0.1 mole) lauryl amines.
Claims (2)
1, a kind of chelate surfactant is characterized in that having following chemical structural formula:
X wherein
2=O, R
2=H, X
1=O or N, R
1=aliphatic group;
Perhaps X wherein
1=O, R
1=H, X
2=O or N, R
2=aliphatic group.
2, chelate surfactant according to claim 1 is characterized in that: the aliphatic group carbon atom quantity is 1 to 30 carbon.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB200510016660XA CN1317061C (en) | 2005-03-30 | 2005-03-30 | Chelated surfacant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB200510016660XA CN1317061C (en) | 2005-03-30 | 2005-03-30 | Chelated surfacant |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1698942A CN1698942A (en) | 2005-11-23 |
CN1317061C true CN1317061C (en) | 2007-05-23 |
Family
ID=35475291
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB200510016660XA Expired - Fee Related CN1317061C (en) | 2005-03-30 | 2005-03-30 | Chelated surfacant |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1317061C (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9445640B2 (en) | 2012-02-20 | 2016-09-20 | Nike, Inc. | Article of footwear incorporating a knitted component with a tongue |
US9510636B2 (en) | 2012-02-20 | 2016-12-06 | Nike, Inc. | Article of footwear incorporating a knitted component with an integral knit tongue |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108940601B (en) * | 2017-05-24 | 2022-03-18 | 中蓝连海设计研究院有限公司 | Application and use method of aminodisuccinic acid or iminodisuccinic acid salt |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1059930A (en) * | 1990-08-17 | 1992-04-01 | 普罗格特-甘布尔公司 | Detergent composition |
-
2005
- 2005-03-30 CN CNB200510016660XA patent/CN1317061C/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1059930A (en) * | 1990-08-17 | 1992-04-01 | 普罗格特-甘布尔公司 | Detergent composition |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9445640B2 (en) | 2012-02-20 | 2016-09-20 | Nike, Inc. | Article of footwear incorporating a knitted component with a tongue |
US9474320B2 (en) | 2012-02-20 | 2016-10-25 | Nike, Inc. | Article of footwear incorporating a knitted component with a tongue |
US9510636B2 (en) | 2012-02-20 | 2016-12-06 | Nike, Inc. | Article of footwear incorporating a knitted component with an integral knit tongue |
Also Published As
Publication number | Publication date |
---|---|
CN1698942A (en) | 2005-11-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1312811A (en) | Bleach catalysts and formulations containing them | |
CN1033226C (en) | Preparation of alkoxyalkanoic acids | |
CN101531954B (en) | Green general-purpose cleaning agent | |
CN103601657B (en) | CLT acid factory effluent stoste prepares method and the compound product of high efficiency water reducing agent monomer | |
CN1317061C (en) | Chelated surfacant | |
CN106008266B (en) | Green preparation method of hydroximic acid rare earth flotation reagent | |
CN100588646C (en) | Industrial preparation method for 3-amino-2, 2-dimethyl propionamide | |
DE2248708B2 (en) | Detergent | |
CN101497564A (en) | Method for synthesizing aliphatic alcohol polyethenoxy ether carboxylate | |
CN101157053A (en) | Catalyst and use thereof new type solid catalyst as well as its preparing method and usage | |
CN1733687A (en) | A (methyl) higher aliphatic acrylate preparation method | |
CN109232178B (en) | Novel method for preparing high-purity hydroxytyrosol | |
EP0396999B1 (en) | 2-Methyl- and 2-hydroxymethyl-serin-N,N-diacetic acids and their derivatives | |
CN102251249B (en) | High-efficiency corrosion-retarding detergent for cobalt-base alloy | |
CN105218544B (en) | A kind of synthetic method of Eliquis intermediate | |
CN102382034A (en) | Synthetic method of N-amino-3-azabicyclo[3,3,0]octane hydrochloride | |
CN103788010B (en) | Febuxostat intermediate and preparation method thereof | |
JP2013529237A (en) | Tris (2-hydroxyphenyl) methane derivative and production and use thereof | |
JP2015501323A (en) | Vinyl monomers with chelating functionality | |
CN104387238A (en) | Preparation method of branched alkyl phenol | |
CN101613337A (en) | The preparation method of salicyl fluorone | |
CN103183621B (en) | Calix[4]arene derivative, non-phosphorus scale inhibition, dispersion and corrosion inhibition agent, preparation method and application | |
CN1569796A (en) | Clean production process of soap | |
JPH11158130A (en) | Production of aminopolycarboxylic acid | |
KR20020023132A (en) | Process for producing poly(meth)acrylates having reduced matal content |
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 | ||
C17 | Cessation of patent right | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20070523 |