CN1065654A - A kind of method of producing dihydroxyphenyl propane - Google Patents
A kind of method of producing dihydroxyphenyl propane Download PDFInfo
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- CN1065654A CN1065654A CN 91106075 CN91106075A CN1065654A CN 1065654 A CN1065654 A CN 1065654A CN 91106075 CN91106075 CN 91106075 CN 91106075 A CN91106075 A CN 91106075A CN 1065654 A CN1065654 A CN 1065654A
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- dihydroxyphenyl propane
- phenol
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- aromatic hydrocarbon
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Abstract
A kind of phenol and acetone of adopting is the method that raw material is produced dihydroxyphenyl propane, it is to be main catalyzer with nascent state hydrogenchloride and sulfuric acid, thioglycolate salt or Thiovanic acid and aluminium dihydrogen tripolyphosphate are cocatalyst, in aromatic hydrocarbon solvent, make phenol condensation with acetone become dihydroxyphenyl propane.It and existing method compare, and it is simple to have technology, and flow process is short, and equipment is few, characteristics such as construction investment province.The dihydroxyphenyl propane quality is good, meets the service requirements of polycarbonate production.
Description
The present invention relates to a kind of is the productive method of chemical engineering that raw material is produced dihydroxyphenyl propane with phenol, acetone.
Dihydroxyphenyl propane, two [4-the hydroxy phenyl]-propane of formal name used at school 2.2-are produced dihydroxyphenyl propane because of using the catalyzer difference, divide sulfuric acid process, hydrogen chloride and ion-exchange-resin process.Sulfuric acid process is primary method, and its technology is simple, and flow process is short, and equipment is few, is easy to industrialization, but its quality product is low, does not reach the service requirements of polycarbonate.Generally believe abroad at present that advanced method is the hydrogen chloride of U.S.'s Hooke (Hoo-Ker) company.It is with acetone and excessive phenol, mol ratio 1: 6, makees catalyzer with gas chlorination hydrogen, carries out under 50-60 ℃ condensation reaction 8-9 hour.Reaction is produced thing through stripping tower, steams water, and the mixture of hydrogenchloride and part phenol separates this mixture decant, and water steams hydrogenchloride, returns condensation and recycles, remaining sour water discharging; Organic phase is returned again into stripping tower.Bottoms from stripping tower is emitted at first steams phenol through steaming the phenol tower, and phenol also returns condensation, and bottoms steams the low isomer that boils earlier again through two rectifying tower; Under high vacuum, steam dihydroxyphenyl propane again, under pressure, make the dihydroxyphenyl propane and the benzene dissolving that steam, and crystallization in benzene, separate, obtain refining dihydroxyphenyl propane after the drying.Residue behind low boil isomer and the refinement mother liquor steaming benzene is by product, accounts for the 10-20% of dihydroxyphenyl propane.The Hooke corportate law, the quality height of dihydroxyphenyl propane meet the service requirements that polycarbonate is produced, but its technical process is long, and whole production system is under the corrosive nature of hydrogenchloride, and high to the material requirement of tower, still, machine, pump and pipeline, equipment life is short.Particularly under high vacuum (residual voltage 0.5-2mmHg), dihydroxyphenyl propane be vaporized before decomposition temperature steam, equipment performance is proposed higher requirement, operation control more complicated, construction investment is big.
The objective of the invention is to make primary sulfuric acid process dihydroxyphenyl propane technology to be improved, under the prerequisite that keeps characteristics such as its flow process is short, equipment is few, technology is simple, produce the high quality dihydroxyphenyl propane that meets polycarbonate production service requirements.
The object of the present invention is achieved like this: adopt the hydrogenchloride and the sulfuric acid of nascent state to make main catalyzer, thioglycolate salt or Thiovanic acid and tripolyphosphate two aluminium are done cocatalyst, in aromatic hydrocarbon solvent, make phenol condensation with acetone generate dihydroxyphenyl propane.The employed nascent state hydrogenchloride of condensation is by the generation that interacts in condensation reaction of sulfuric acid and Repone K or sodium-chlor.The dihydroxyphenyl propane that condensation generates obtains the finished product dihydroxyphenyl propane through washing, crystallization.Finish the solvent aromatic hydrocarbon of telling after the condensation reaction,, make it remove the dihydroxyphenyl propane isomer and obtain regeneration with sodium hydroxide solution washing.
The present invention is owing to adopt nascent state hydrogenchloride and the effect of vitriolic dual catalytic, strengthened the main reaction process of condensation, suppressed the generation of by product, thereby the yield height of producing, good product quality, can produce the dihydroxyphenyl propane that meets polycarbonate production service requirements, this is that existing sulfuric acid process is not accomplished.Because technology of the present invention compares with the hydrogen chloride that generally adopts, it is short to have flow process, and equipment is few, and corrosion is light, and advantages such as construction investment province are so very easily apply.
Below the invention will be further described.
1, condensation
The main catalyzer of condensation reaction is sulfuric acid and nascent state hydrogenchloride, and nascent state hydrogenchloride is by sulfuric acid and Repone K or sodium-chlor, the generation that interacts in condensation reaction.Cocatalyst is thioglycolate salt or Thiovanic acid and aluminium dihydrogen tripolyphosphate, and aromatic hydrocarbon solvent is a benzene, toluene, dimethylbenzene and chlorobenzene.
With phenol and acetone according to 1: the amount of the mol ratio of 0.25-0.8 joins in the condensation reaction jar, and according to phenol and sulfuric acid with 1: the amount of 0.8-2.0 mol ratio adds sulfuric acid, according to sulfuric acid and Repone K or sodium-chlor with 1: the amount of 0.2-0.9 mol ratio adds Repone K or sodium-chlor, 0.5-5% according to the phenol input amount adds thioglycolate salt or Thiovanic acid and aluminium dihydrogen tripolyphosphate, 1-3 according to the phenol input amount doubly drops into aromatic hydrocarbon, under 15-70 ℃ of temperature stirring reaction 2-12 hour.Its reaction process is:
After reaction finishes, add the water of 2-5 times of resultant dihydroxyphenyl propane, under 80-110 ℃, dilute washing, washing time 0.5-2 hour.Dihydroxyphenyl propane enters the aromatic hydrocarbon organic phase, and sulfuric acid, hydrochloric acid, sal enixum, Repone K etc. are soluble in the aqueous phase.Two are separated, and lower floor is a water, tell as by-product, can adopt to form and put legal system and get vitriolate of tartar, ammonium chloride.The upper strata is an organic phase, and cooling and stirring to 15 ℃ separates out crude bisphenol, extracts aromatic hydrocarbon solvent then out, sends to alkali cleaning regeneration.
2, crystallization
With the crude bisphenol in the condensation jar, by the 4-10 of its weight extraordinarily entry wash, wash temperature 50-120 ℃, churning time 0.1-2.5 hour.After washing finished, dihydroxyphenyl propane was just separated out with the sedimentation from water layer of fusion paste liquid in water, then this fusion paste liquid is put into the aromatic hydrocarbon solvent of crystallization reaction jar, dissolving, cooling, crystal refining.10-40 ℃ of crystallisation by cooling temperature, time 0.1-10 hour.Isolate the dihydroxyphenyl propane of aromatic hydrocarbon mother liquor, after 100 ℃ of dryings, be finished product.Washing water are the recyclable processing of phenolic wastewater in the condensation reaction jar.
3, alkali cleaning regeneration
The solvent aromatic hydrocarbon that condensation is told is put in the alkali cleaning retort, and press the contained total phenol of solvent aromatic hydrocarbon and sodium hydroxide: the amount of 1.0-1.5 mol ratio with 1, dropping into concentration is the sodium hydroxide solution of 5-42%, under 10-80 ℃ of temperature, stirred 0.1-4 hour, and removed the dihydroxyphenyl propane isomer and make aromatic hydrocarbon solvent regeneration.After alkali cleaning finishes, leave standstill two phase stratification, the upper strata is an organic phase, and promptly the aromatic hydrocarbon after the regeneration recycles again.Lower floor is a water, and promptly the sodium salt of dihydroxyphenyl propane isomer is done the by-product processing and utilization after telling.
Now be described in detail technical process of the present invention in conjunction with the embodiments
Embodiment one
With 190 kilograms of 99% phenol, 65.1 fens jin of 98% acetone, 240 fens jin of 98% industrial sulphuric acid, 112.9 kilograms in 95% Repone K, 94 kilograms of toluene, 2.8 kilograms of barium thioglycolate and aluminium dihydrogen tripolyphosphates get 197.5 kilograms of dihydroxyphenyl propanes through condensation, washing, crystallization, yield 86.5%, the main technique condition of this example is:
(1), condensation
Mol ratio, phenol: acetone=1: 0.5-0.6
Sulfuric acid: Repone K=1: 0.55-0.65
Phenol: sulfuric acid=1: 1.1-1.3
Weight ratio, phenol: toluene=1: 2.4-2.6
Phenol: barium thioglycolate and aluminium dihydrogen tripolyphosphate=
1∶0.01-0.02
Temperature of reaction: 45-55 ℃
Churning time: 4-8 hour
(2) dilution washing
Dilute wash temperature: 90-100 ℃
Dilution washing time: 2 hours
(3), crystallization
Water washing temperature: 70-100 ℃
The water washing time: 2 hours
In toluene crystallization cooling temperature: 10-20 ℃
Crystallization time in toluene: 3 hours
(4), regeneration
Naoh concentration: 10-30%
Mol ratio: total phenol: sodium hydroxide=1: 1.2-1.4
Alkali cleaning temperature: 40-70 ℃
Churning time: 2 hours
Embodiment two
With 95 kilograms of 99% phenol, 29.6 kilograms in 98% acetone, 110 kilograms of 98% industrial sulphuric acids, 39.6 kilograms in 95% Repone K, 43.2 kilograms of dimethylbenzene, 1.9 kilograms of Thiovanic acid and aluminium dihydrogen tripolyphosphates get 97.6 kilograms of dihydroxyphenyl propanes through condensation, washing, crystallization, yield 85.5%, the main technique condition of this example is:
(1), condensation
Mol ratio, phenol: acetone=1: 0.45-0.55
Sulfuric acid: Repone K=1: 0.4-0.5
Phenol: sulfuric acid=1: 1.0-1.2
Weight ratio, phenol: dimethylbenzene=1: 2.2-2.4
Phenol: Thiovanic acid and aluminium dihydrogen tripolyphosphate=
1∶0.01-0.03
Temperature of reaction: 40-45 ℃
Churning time: 4-8 hour
(2), dilution washing
Dilute wash temperature: 90-110 ℃
Dilution washing time: 2 hours
(3), crystallization
Water washing temperature: 90-110 ℃
The water washing time: 1.5 hours
In dimethylbenzene crystallization cooling temperature: 10-20 ℃
Crystallization time in dimethylbenzene: 2 hours
(4), regeneration
Naoh concentration: 15-25%
Mol ratio: total phenol: sodium hydroxide=1: 1.2-1.4
Alkali cleaning temperature: 50-70 ℃
Churning time: 1.5 hours
Embodiment three
With 142.4 kilograms of 99% phenol, 53.3 kilograms in 98% acetone, 202.5 kilograms of 98% industrial sulphuric acids, 67.2 kilograms in 97% sodium-chlor, 51.8 kilograms of chlorinated benzene, 2.6 kilograms of Thioglycolic acid sodium salt and aluminium dihydrogen tripolyphosphates get 151.9 kilograms of dihydroxyphenyl propanes through condensation, washing, crystallization, yield 88.7%, the main technique condition of this example is:
(1), condensation
Mol ratio, phenol: acetone=1: 0.55-0.65
Sulfuric acid: Repone K=1: 0.5-0.6
Phenol: sulfuric acid=1: 1.3-1.4
Weight ratio, phenol: toluene=1: 2.4-2.5
Phenol: Thioglycolic acid sodium salt and aluminium dihydrogen tripolyphosphate=
1∶0.015-0.025
Temperature of reaction: 45-50 ℃
Churning time: 4-8 hour
(2), dilution washing
Dilute wash temperature: 90-105 ℃
Dilution washing time: 2 hours
(3), crystallization
Water washing temperature: 90-105 ℃
The water washing time: 1.5 hours
In chlorinated benzene crystallization cooling temperature: 10-20 ℃
Crystallization time in chlorinated benzene: 2 hours
(4), regeneration
Naoh concentration: 15-25%
Mol ratio, total phenol: sodium hydroxide=1: 1.2-1.4
Alkali cleaning temperature: 50-70 ℃
Churning time: 1.5 hours
Example one, two, three products quality index
Quality project quality index
Fusing point 155-157 ℃
Colourity≤130(dissolves method)
Phenol content≤0.1%
Iron level≤3PPM
Moisture content≤0.1%
The appearance white crystalline powder is transparent inorganic tool impurity liquid after 180 ℃ of fusions
Claims (6)
1, a kind of phenol, acetone of adopting is the method that raw material is produced dihydroxyphenyl propane, it is characterized in that adopting the hydrogenchloride of nascent state and sulfuric acid to make main catalyzer, thioglycolate salt or Thiovanic acid and tripolyphosphate two aluminium are done cocatalyst, in aromatic hydrocarbon solvent, make phenol condensation with acetone generate dihydroxyphenyl propane, the employed nascent state hydrogenchloride of condensation, by the generation that interacts in condensation reaction of sulfuric acid and Repone K or sodium-chlor, the dihydroxyphenyl propane that condensation generates obtains the finished product dihydroxyphenyl propane through washing, crystallization.
2, the method for producing dihydroxyphenyl propane according to claim 1, it is characterized in that the mol ratio of sulfuric acid and Repone K or sodium-chlor is 1 in condensation reaction: 0.2-0.9, occurrence temperature is 15-70 ℃.
3, the method for producing dihydroxyphenyl propane according to claim 1 and 2, the mol ratio that it is characterized in that phenol and acetone is 1: 0.25-0.8, phenol and vitriolic mol ratio are 1: 0.8-2.0, the input amount of thioglycolate salt or Thiovanic acid and aluminium dihydrogen tripolyphosphate is the 0.5-5% of phenol weight, the input amount of aromatic hydrocarbon is 1-3 a times of phenol weight, setting-up point is 15-70 ℃, and churning time is 2-12 hour.
4, the method for producing dihydroxyphenyl propane according to claim 1 is characterized in that making the dihydroxyphenyl propane of telling after the condensation to dissolve into paste liquid in water, dissolves temperature 50-120 ℃, churning time 0.1-2.5 hour.
5, the method for producing dihydroxyphenyl propane according to claim 1 is characterized in that the dihydroxyphenyl propane paste liquid that dissolves dissolves, crystallisation by cooling refining in aromatic hydrocarbon, the crystallisation by cooling temperature is 10-40 ℃, and crystallization time is 0.1-10 hour.
6, the method for producing dihydroxyphenyl propane according to claim 1, it is characterized in that reacting the solvent aromatic hydrocarbon of telling after finishing, the washing of employing sodium hydroxide solution, make it remove the dihydroxyphenyl propane isomer and regenerate, concentration of sodium hydroxide solution is 5-42%, the alkali cleaning temperature is 10-80 ℃, and the wash agitation time is 0.1-4 hour.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 91106075 CN1024541C (en) | 1991-04-09 | 1991-04-09 | Preparing method for bisphenol A |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 91106075 CN1024541C (en) | 1991-04-09 | 1991-04-09 | Preparing method for bisphenol A |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1065654A true CN1065654A (en) | 1992-10-28 |
| CN1024541C CN1024541C (en) | 1994-05-18 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 91106075 Expired - Fee Related CN1024541C (en) | 1991-04-09 | 1991-04-09 | Preparing method for bisphenol A |
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| Country | Link |
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| CN (1) | CN1024541C (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101100416B (en) * | 2006-07-03 | 2011-02-16 | 中国科学院上海药物研究所 | Small molecule inhibitor for preventing Alzheimer's disease Abeta polypeptide from fiberizing and its preparation method, pharmaceutical composition and application |
| CN111902387A (en) * | 2017-11-10 | 2020-11-06 | Ddp特种电子材料美国公司 | Catalytic process |
-
1991
- 1991-04-09 CN CN 91106075 patent/CN1024541C/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101100416B (en) * | 2006-07-03 | 2011-02-16 | 中国科学院上海药物研究所 | Small molecule inhibitor for preventing Alzheimer's disease Abeta polypeptide from fiberizing and its preparation method, pharmaceutical composition and application |
| CN111902387A (en) * | 2017-11-10 | 2020-11-06 | Ddp特种电子材料美国公司 | Catalytic process |
| CN111902387B (en) * | 2017-11-10 | 2023-09-05 | Ddp特种电子材料美国有限责任公司 | Catalytic process |
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| Publication number | Publication date |
|---|---|
| CN1024541C (en) | 1994-05-18 |
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