CN107999126A - A kind of catalyst and preparation method and purposes for synthesizing phosphoric acid extraction defoamer - Google Patents
A kind of catalyst and preparation method and purposes for synthesizing phosphoric acid extraction defoamer Download PDFInfo
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- CN107999126A CN107999126A CN201711205734.3A CN201711205734A CN107999126A CN 107999126 A CN107999126 A CN 107999126A CN 201711205734 A CN201711205734 A CN 201711205734A CN 107999126 A CN107999126 A CN 107999126A
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- China
- Prior art keywords
- catalyst
- defoamer
- phosphoric acid
- sodium
- acid extraction
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0215—Sulfur-containing compounds
- B01J31/0229—Sulfur-containing compounds also containing elements or functional groups covered by B01J31/0201 - B01J31/0214
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/02—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof
- C07C303/04—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof by substitution of hydrogen atoms by sulfo or halosulfonyl groups
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- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
Abstract
The present invention relates to a kind of catalyst and preparation method and purposes for synthesizing phosphoric acid extraction defoamer, each component mass percentage, the catalyst to be prepared according to the following steps:1) 40~50% diisooctyl maleates, 5~20% diisooctyl succinate sodium sulfonates are uniformly mixed;2) 10~15% sodium pyrosulfite is dissolved in spare in 25~35% water;3) it is 100~105 DEG C, under normal pressure in temperature, the sodium metabisulfite solution prepared in step 2) is added drop-wise in the system of step 1) in 1~4h, the reaction was continued 5~8 it is small when, products therefrom for homogeneous phase transparent liquid be synthesize phosphoric acid extraction defoamer catalyst.The catalyst of the present invention may not necessarily introduce exogenous impurity, and the post processing that can be omitted after reaction removes catalyst operation.Compared with existing catalyst, catalyst of the invention have the characteristics that excellent catalytic effect, it is easy to operate, be easily obtained, be of low cost, obtained anti-foam product purity it is high.
Description
Technical field
The present invention relates to a kind of catalyst and preparation method and purposes for synthesizing phosphoric acid extraction defoamer.
Background technology
Since this phosphoric acid extraction defoamer needs the reactant aqueous solution using succinic acid dibasic acid esters and sodium pyrosulfite, the reaction
It is two phase reaction, reaction rate is limited by phase contact area size.Generally use raises temperature and additional phase transfer catalyst
Method.Rise temperature not only easily makes ester hydrolysis, but also sulfonating agent is decomposed aggravation, therefore can cause sulfonating agent loss and sulfonation
Reaction is incomplete.Passing through the method heated under closed system, it is possible to reduce sulfur dioxide escapes and suppresses the decomposition of sulfonating agent,
But the resistance to pressure requirement to reaction unit is so added again.The method of extra catalyst often makes the final product of reaction again
In contained impurity level increase, product quality is impacted.
The content of the invention
The purpose of the invention is to overcome defect and problem existing in the prior art, and provide a kind of synthesis phosphoric acid extraction
The catalyst and preparation method and purposes of defoamer.Catalyst provided by the invention avoids introduced miscellaneous of extra catalyst
Matter so that obtained product purity is high.
The present invention is realized by following technology:
A kind of catalyst for synthesizing phosphoric acid extraction defoamer, each component mass percentage, it is characterised in that the catalysis
Agent is prepared according to the following steps:1) by 40~50% diisooctyl maleates, 5~20% succinic acid di-isooctyl sulfonic acid
Sodium is uniformly mixed;2) 10~15% sodium pyrosulfite is dissolved in spare in 25~35% water;3) temperature for 100~105 DEG C,
Under normal pressure, the sodium metabisulfite solution prepared in step 2) is added drop-wise in the system of step 1) in 1~4h, the reaction was continued 5
~8 it is small when, products therefrom for homogeneous phase transparent liquid be synthesize phosphoric acid extraction defoamer catalyst.
It is just pungent for 30~70% diisooctyl succinate sodium sulfonates or succinic acid two that the catalyst contains mass fraction
Ester sodium sulfonate.
A kind of preparation method for the catalyst for synthesizing phosphoric acid extraction defoamer, each component mass percentage, its feature exist
Carried out according to the following steps:1) 40~50% diisooctyl maleates, 5~20% diisooctyl succinate sodium sulfonates are mixed
Close uniform;2) 10~15% sodium pyrosulfite is dissolved in spare in 25~35% water;3) it is 100~105 DEG C, normal pressure in temperature
Under, the sodium metabisulfite solution prepared in step 2) is added drop-wise in the system of step 1) in 1~4h, it is 5~8 small that the reaction was continued
When, products therefrom as synthesizes the catalyst of phosphoric acid extraction defoamer for the liquid of homogeneous phase transparent.
The aqueous solution that the catalyst of above-mentioned synthesis phosphoric acid extraction defoamer is used for succinic acid dibasic acid esters and sodium pyrosulfite is anti-
Ying Zhong, additive amount account for the 5~20% of succinic acid dibasic acid esters and sodium pyrosulfite total amount.
Catalyst provided by the invention has the features such as Catalysis Rate is fast, is easily obtained, of low cost, and will not introduce
Exogenous impurity, the catalyst not only reduced after reaction remove link, reduce production cost, and high-purity can be made
Phosphoric acid extraction anti-foam product.
Embodiment
With reference to embodiment, the invention will be further described.
Embodiment 1
1) it is 8.1kg diisooctyl maleates, 0.8kg diisooctyl succinate sodium sulfonates is spare after mixing;
2) 2.1kg sodium pyrosulfites are dissolved in 5.2kg water, it is spare after stirring and dissolving;
3) it is 105 DEG C, under normal pressure in temperature, sodium metabisulfite solution made from step 2) is added drop-wise to step 1) in 1h
In system in, after being added dropwise, continue insulation reaction 5 it is small when, institute product for homogeneous phase transparent liquid be synthesis phosphoric acid
Extract the catalyst of defoamer.
Embodiment 2
1) the diisooctyl succinate sodium sulfonate solution of 3810kg diisooctyl maleates, 1865kg are uniformly mixed
It is spare afterwards;
2) 950kg sodium pyrosulfites are dissolved in 2785kg fresh waters, it is spare after stirring and dissolving;
3) it is 103 DEG C, under normal pressure in temperature, the body 1) solution of sodium pyrosulfite made from 2) is added drop-wise in 3h in
In system, after being added dropwise, continue insulation reaction 7 it is small when, institute product for homogeneous phase transparent liquid be synthesis phosphoric acid extraction disappear
The catalyst of infusion.
Embodiment 3
1) the diisooctyl succinate sodium sulfonate solution of 45kg diisooctyl maleates, 15kg are uniformly mixed standby
With;
2) 15kg sodium pyrosulfites are dissolved in 25kg fresh waters, it is spare after stirring and dissolving;
3) it is 100 DEG C, under normal pressure in temperature, the body 1) solution of sodium pyrosulfite made from 2) is added drop-wise in 4h in
In system, after being added dropwise, continue insulation reaction 8 it is small when, institute product for homogeneous phase transparent liquid be synthesis phosphoric acid extraction disappear
The catalyst of infusion.
Comparative example 1
1) 8.1kg diisooctyl maleates are added spare in reaction system;
2) 2.1kg sodium pyrosulfites are dissolved in 5.2kg water, it is spare after stirring and dissolving;
3) it is 105 DEG C, under normal pressure in temperature, sodium metabisulfite solution made from step 2) is added drop-wise to step 1) in 1h
In system in, after being added dropwise, continue insulation reaction 8 it is small when, reaction system is still oil/water two-phase system, i.e., all reactions
Thing cannot be reacted.
Claims (4)
1. a kind of catalyst for synthesizing phosphoric acid extraction defoamer, each component mass percentage, by being characterized in that the catalysis
Agent is prepared according to the following steps:1) by 40~50% diisooctyl maleates, 5~20% succinic acid di-isooctyl sulfonic acid
Sodium is uniformly mixed;2) 10~15% sodium pyrosulfite is dissolved in spare in 25~35% water;3) temperature for 100~105 DEG C,
Under normal pressure, the sodium metabisulfite solution prepared in step 2) is added drop-wise in the system of step 1) in 1~4h, the reaction was continued 5
~8 it is small when, products therefrom for homogeneous phase transparent liquid be synthesize phosphoric acid extraction defoamer catalyst.
A kind of 2. catalyst for synthesizing phosphoric acid extraction defoamer according to claim 1, it is characterised in that:The catalysis
It is 30~70% diisooctyl succinate sodium sulfonates or succinic acid di-n-octyl sodium sulfonate that agent, which contains mass fraction,.
3. a kind of preparation method for the catalyst for synthesizing phosphoric acid extraction defoamer, each component quality hundred described in a kind of claim 1
Fraction meter, it is characterised in that carry out according to the following steps:1) by 40~50% diisooctyl maleates, 5~20% succinic acid
Di-isooctyl sodium sulfonate is uniformly mixed;2) 10~15% sodium pyrosulfite is dissolved in spare in 25~35% water;3) in temperature
For under 100~105 DEG C, normal pressure, the sodium metabisulfite solution prepared in step 2) to be added drop-wise to the system of step 1) in 1~4h
In, the reaction was continued 5~8 it is small when, products therefrom for homogeneous phase transparent liquid be synthesize phosphoric acid extraction defoamer catalyst.
A kind of 4. purposes of catalyst for synthesizing phosphoric acid extraction defoamer according to claim 1 or 2, it is characterised in that:
Catalyst prepared by claim 1 or 2 is used in the reactant aqueous solution of succinic acid dibasic acid esters and sodium pyrosulfite, and additive amount accounts for fourth
The 5~20% of two acid diesters and sodium pyrosulfite total amount.
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101284806A (en) * | 2008-06-06 | 2008-10-15 | 江苏省海安石油化工厂 | Clean production process for sodium diethylhexyl sulfosuccinate |
CN101696224A (en) * | 2009-11-02 | 2010-04-21 | 甘肃省化工研究院 | Method for synthesizing di(isooctyl) phosphate |
CN102391158A (en) * | 2011-08-04 | 2012-03-28 | 浙江合诚化学有限公司 | Preparation method of isooctanol polyoxypropylene ether sodium sulfosuccinate diester |
CN102599326A (en) * | 2012-03-23 | 2012-07-25 | 山东省农业科学院农产品研究所 | Backward extraction method for reversed micellar extraction of soybean protein |
CN104829503A (en) * | 2015-05-27 | 2015-08-12 | 北京康远制药有限公司 | Method for preparing high-purity docusate sodium |
-
2017
- 2017-11-27 CN CN201711205734.3A patent/CN107999126A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101284806A (en) * | 2008-06-06 | 2008-10-15 | 江苏省海安石油化工厂 | Clean production process for sodium diethylhexyl sulfosuccinate |
CN101696224A (en) * | 2009-11-02 | 2010-04-21 | 甘肃省化工研究院 | Method for synthesizing di(isooctyl) phosphate |
CN102391158A (en) * | 2011-08-04 | 2012-03-28 | 浙江合诚化学有限公司 | Preparation method of isooctanol polyoxypropylene ether sodium sulfosuccinate diester |
CN102599326A (en) * | 2012-03-23 | 2012-07-25 | 山东省农业科学院农产品研究所 | Backward extraction method for reversed micellar extraction of soybean protein |
CN104829503A (en) * | 2015-05-27 | 2015-08-12 | 北京康远制药有限公司 | Method for preparing high-purity docusate sodium |
Non-Patent Citations (1)
Title |
---|
张万忠 等: "琥珀酸二异辛酯磺酸钠制备的影响因素研", 《化学试剂》 * |
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