CN103450272A - Phosphorus-modified phenolic resin and preparation method thereof - Google Patents

Phosphorus-modified phenolic resin and preparation method thereof Download PDF

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Publication number
CN103450272A
CN103450272A CN2013103190319A CN201310319031A CN103450272A CN 103450272 A CN103450272 A CN 103450272A CN 2013103190319 A CN2013103190319 A CN 2013103190319A CN 201310319031 A CN201310319031 A CN 201310319031A CN 103450272 A CN103450272 A CN 103450272A
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modified phenolic
phosphorus
reaction
butylphenol
tert
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关炽昌
刘涛
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GUANGXI TENGXIAN TONGXUAN LIXIN CHEMICAL Co Ltd
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GUANGXI TENGXIAN TONGXUAN LIXIN CHEMICAL Co Ltd
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Publication of CN103450272A publication Critical patent/CN103450272A/en
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Abstract

The invention discloses a phosphorus-modified phenolic resin material with a new chemical structural formula and a preparation method thereof. The method comprises the following steps: polycondensing paratert-butyl phenol and formaldehyde under the action of a catalyst to obtain a phenol aldehyde condensation intermediate; and reacting the intermediate with monobasic alcohols and organic phosphorus heterocyclic compounds at a preset temperature for preset time under catalytic conditions to prepare the phosphorus-modified phenolic resin. The method solves the problem of complete dependency on the phosphorus-modified phenolic resin imported from abroad in the past, and enhances the heat resistance, binding strength, peel strength, favorable space size, excellent electric properties, mechanical strength and other physicochemical performance indexes of the original phosphorus-modified phenolic resin, so that the phosphorus-modified phenolic resin has better application properties when being applied to the field of electronic chemicals.

Description

Phosphorus modified phenolic resins and preparation method thereof
Technical field
The invention belongs to phosphorus modified epoxy field, be specifically related to a kind of phosphorus modified phenolic resins and preparation method thereof.
Background technology
At present, domestic phosphorus modified resin system also only is confined at the phosphorus modified epoxy resin system, is mainly used in and take the electronic seal plastic coating as main field of coating.In recent years along with the service requirements of field of coating, the continuous lifting of application performance, physics to the phosphorus modified epoxy resin curing agent, chemistry application performance parameter request is also had higher requirement thereupon, general phosphorus modified epoxy can not meet the application requiring of this electronics application high-end field, answer the special requirement in market, the U.S. in 20 record at the beginning of, some international large chemical company starts to need to explore by organic phosphates heterogeneous ring compound class as luxuriant and rich with fragrance as phosphorus for satisfying the market, annular phosphate class raw material is applied in dihydroxyphenyl propane and modified formaldehyde resin, through several years, with the combination of application, explore, produce phosphorus modified bisphenol A urea formaldehyde in research and development in recent years, and it is successfully applied to the halogen-free flame-resistant electronic field.So far, along with the raising day by day of China's field of coating application demand, in the high-end field of this application, just rely on the import of this type of phosphorus modified phenolic resins fully, seriously limited the development of China's field of coating, and expensive, and each performance also has much room for improvement.
Summary of the invention
The invention provides a kind of new phosphorus modified phenolic resins material and preparation method thereof, solved the problem that in the past relies on external import phosphorus modified phenolic resins fully.
In order to solve the problems of the technologies described above, the technical solution adopted in the present invention is:
The molecular structural formula of phosphorus modified phenolic resins of the present invention is:
Figure DEST_PATH_362316DEST_PATH_IMAGE001
In formula ,-R1 representative-C 3h 7,-C 4h 9,-C 5h 11; N value 0-3 ,-R2-representative
Figure 2013103190319100002DEST_PATH_DEST_PATH_IMAGE002
;
The preparation method of above-mentioned phosphorus modified phenolic resins comprises the following steps:
A, p-tert-butylphenol, formaldehyde and water are added in reaction vessel, with the catalyst reaction, obtain the phenol formaldehyde condensation body, temperature of reaction is 50 ℃~100 ℃, and the reaction times is 1~5 hour; The mol ratio of described p-tert-butylphenol and described formaldehyde is 1:2~3, the mass percent that described catalyzer accounts for the total mass of described formaldehyde and described p-tert-butylphenol is 1%~5%, and the mass percent that described water accounts for the total mass of described formaldehyde and described p-tert-butylphenol is 10%~15%;
B, introduce monohydroxy-alcohol, making catalyzer with aluminium sesquioxide and sulfuric acid, to carry out take monolateral end-blocking be the etherification reaction of leading, and temperature of reaction is 80 ℃~120 ℃, and the reaction times is 4~6 hours; The mol ratio of described p-tert-butylphenol and described monohydroxy-alcohol is 1:2~5, the mass percent that described aluminium sesquioxide accounts for the total mass of described p-tert-butylphenol is 0.5%~1.5%, and the mass percent that described sulfuric acid accounts for the total mass of described p-tert-butylphenol is 0.1%~0.8%;
C, introducing 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide carry out graft reaction and obtain this phosphorus modified phenolic resins, and temperature of reaction is 100 ℃~160 ℃, 9~11 hours reaction times; The mol ratio of described 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide and described p-tert-butylphenol is 0.8~1.5:1;
Described catalyzer is a kind of in an acidic catalyst, basic catalyst;
Described an acidic catalyst is a kind of of tosic acid, hydrochloric acid, sulfuric acid, phosphoric acid, oxalic acid;
Described basic catalyst is a kind of of sodium hydroxide, potassium hydroxide, calcium hydroxide, triethylamine, ammoniacal liquor;
Described monohydroxy-alcohol is a kind of of butanols, propyl alcohol, amylalcohol.
Owing to adopting technique scheme, the present invention has following beneficial effect:
1, the invention solves the problem that in the past relies on external import phosphorus modified phenolic resins fully, promoted the physical and chemical performance indexs such as heat-resisting, the bonding and stripping strength of original phosphorus modified epoxy thing, good bulk and excellent electrical property and physical strength, the coating performance that makes this phosphorus modified phenolic resins be applied to the electronic chemical product field is better.
2, optimize the working condition of traditional pure phenolic resin, adopted solvent-free reaction pattern, environmental contamination reduction.
3, take p-tert-butylphenol first prepares resol as matrix, and then by the organic phosphates heterogeneous ring compound as 9, mix-10-phospho hetero phenanthrene-10-oxide compound of 10-dihydro-9-oxy and monohydroxy-alcohol carry out the even end-blocking of methylol under the catalytic condition of setting, form the phosphorus modified phenolic resins of serial different physical and chemical performances, its adhesiveproperties, thermally-stabilised, ageing-resistant, machinability, electric property, film forming stability can etc. better in the single phosphorus modified bisphenol A urea formaldehyde product of import.
4, can, according to the electronics coating process requirement of different manufacturers, by the proportioning of adjusting raw material phenol, the kind of alcohol etc., make the epoxy hardener phosphorus modified phenolic resin fat prod that more adapts to different service requirementss.
Embodiment
Table 1, table 2 are reaction raw materials component and the reaction conditions in embodiment 1~embodiment 10, and wherein the phenol described in embodiment 1~embodiment 10 is p-tert-butylphenol.
According to following preparation steps, prepared by reaction raw materials component and reaction conditions that associative list 1, table 2 provide:
A, get phenol, formaldehyde and water respectively and join in four-hole boiling flask and mix, then add catalyst mix even, four-hole boiling flask is put into to the electric mantle heating and carry out condensation reaction and obtain the phenol formaldehyde condensation body, after cooling, it is emitted, minute remove residual moisture;
In B, phenol formaldehyde condensation body add-back four-hole bottle that steps A is obtained, add monohydroxy-alcohol to mix, then add aluminium sesquioxide and sulfuric acid to make catalyzer, insulation reflux dewatering reaction after heating up, carry out take monolateral end-blocking as main etherification reaction to the phenol formaldehyde condensation body;
C, in step B, add 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, insulation dehydration graft reaction after heating up, the remaining methylol end-blocking grafting by the other side of phenol formaldehyde condensation body, obtain this phosphorus modified phenolic resins.
According to table 1, table 2 and above-mentioned preparation process, the chemical structural formula that embodiment 1~embodiment 10 obtains this phosphorus modified phenolic resins is evenly:
Figure DEST_PATH_645530DEST_PATH_IMAGE001
In formula ,-R1 representative-C 3h 7,-C 4h 9,-C 5h 11; N value 0-3 ,-R2-representative .
Phosphorus modified phenolic resins of the present invention can add ether solvent, adjusts flowing property, viscosity, solid content and the film forming speed of material, so that pack, use and construct.
Table 1
Figure 2013103190319100002DEST_PATH_IMAGE001
Table 2
Figure 2013103190319100002DEST_PATH_IMAGE002
Table 3, table 4 are Performance Detection that the solidifying agent that obtains after phosphorus modified phenolic resins of the present invention adds redix carries out, and with the Performance Ratio of external two company's products, result is as follows:
Table 3
Figure 2013103190319100002DEST_PATH_IMAGE003
Table 4
Figure 2013103190319100002DEST_PATH_IMAGE004

Claims (2)

1. a phosphorus modified phenolic resins is characterized in that comprising following chemical structure:
Figure 2013103190319100001DEST_PATH_DEST_PATH_IMAGE001
In formula ,-R1 representative-C 3h 7,-C 4h 9,-C 5h 11; N value 0-3 ,-R2-representative .
2. the preparation method of a phosphorus modified phenolic resins is characterized in that:
The chemical structural formula of described phosphorus modified phenolic resins is:
In formula ,-R1 representative-C 3h 7,-C 4h 9,-C 5h 11; N value 0-3 ,-R2-representative
Figure DEST_PATH_803991DEST_PATH_IMAGE002
;
The preparation of described phosphorus modified phenolic resins comprises the steps:
A, p-tert-butylphenol, formaldehyde and water are added in reaction vessel, with the catalyst reaction, obtain the phenol formaldehyde condensation body, temperature of reaction is 50 ℃~100 ℃, and the reaction times is 1~5 hour; The mol ratio of described p-tert-butylphenol and described formaldehyde is 1:2~3, the mass percent that described catalyzer accounts for the total mass of described formaldehyde and described p-tert-butylphenol is 1%~5%, and the mass percent that described water accounts for the total mass of described formaldehyde and described p-tert-butylphenol is 10%~15%;
B, introduce monohydroxy-alcohol, making catalyzer with aluminium sesquioxide and sulfuric acid, to carry out take monolateral end-blocking be the etherification reaction of leading, and temperature of reaction is 80 ℃~120 ℃, and the reaction times is 4~6 hours; The mol ratio of described p-tert-butylphenol and described monohydroxy-alcohol is 1:2~5, the mass percent that described aluminium sesquioxide accounts for the total mass of described p-tert-butylphenol is 0.5%~1.5%, and the mass percent that described sulfuric acid accounts for the total mass of described p-tert-butylphenol is 0.1%~0.8%;
C, introducing 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide carry out graft reaction and obtain this phosphorus modified phenolic resins, and temperature of reaction is 100 ℃~160 ℃, 9~11 hours reaction times; The mol ratio of described 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide and described p-tert-butylphenol is 0.8~1.5:1;
Described catalyzer is a kind of in an acidic catalyst, basic catalyst;
Described an acidic catalyst is a kind of of tosic acid, hydrochloric acid, sulfuric acid, phosphoric acid, oxalic acid;
Described basic catalyst is a kind of of sodium hydroxide, potassium hydroxide, calcium hydroxide, triethylamine, ammoniacal liquor;
Described monohydroxy-alcohol is a kind of of butanols, propyl alcohol, amylalcohol.
CN2013103190319A 2013-07-27 2013-07-27 Phosphorus-modified phenolic resin and preparation method thereof Pending CN103450272A (en)

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Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102378802A (en) * 2009-04-01 2012-03-14 韩国埃迪碧化学株式会社 Organic phosphorus-based flame retardant and process for producing the same
CN103172812A (en) * 2013-03-15 2013-06-26 山东圣泉化工股份有限公司 Preparation method of phosphorous-containing phenol formaldehyde resin and resin prepared

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102378802A (en) * 2009-04-01 2012-03-14 韩国埃迪碧化学株式会社 Organic phosphorus-based flame retardant and process for producing the same
CN103172812A (en) * 2013-03-15 2013-06-26 山东圣泉化工股份有限公司 Preparation method of phosphorous-containing phenol formaldehyde resin and resin prepared

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Application publication date: 20131218