CN111704684A - Method for modifying C5/C9 copolymer resin by using peracetic acid - Google Patents

Method for modifying C5/C9 copolymer resin by using peracetic acid Download PDF

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CN111704684A
CN111704684A CN202010692971.2A CN202010692971A CN111704684A CN 111704684 A CN111704684 A CN 111704684A CN 202010692971 A CN202010692971 A CN 202010692971A CN 111704684 A CN111704684 A CN 111704684A
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resin
catalyst
solvent
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copolymer resin
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CN111704684B (en
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王斌
孙向东
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Henghe Materials and Science Technology Co Ltd
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F240/00Copolymers of hydrocarbons and mineral oils, e.g. petroleum resins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F6/00Post-polymerisation treatments
    • C08F6/06Treatment of polymer solutions
    • C08F6/10Removal of volatile materials, e.g. solvents

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  • Chemical Kinetics & Catalysis (AREA)
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Abstract

The invention relates to a method for modifying C5/C9 copolymer resin by using peracetic acid, which comprises the following steps: mixing C5 and C9 fractions to obtain a polymerization raw material, carrying out catalytic polymerization to obtain a polymerization solution, carrying out alkaline washing and water elution catalysis, and carrying out steam stripping to remove a solvent to obtain a molten resin solution; and mixing and modifying the molten resin liquid and peroxyacetic acid in a double-screw stirring extruder to obtain the modified C5/C9 copolymer resin. The method has the advantages that peroxyacetic acid is added as an initiator to induce C5/C9 copolymerized petroleum resin to generate ring-opening reaction, so that the unsaturation degree of the petroleum resin product is reduced, and the odor of the resin is reduced; meanwhile, the method has the advantages of low cost, simple process and good application prospect.

Description

Method for modifying C5/C9 copolymer resin by using peracetic acid
Technical Field
The invention belongs to the field of petroleum resin, and particularly relates to a method for modifying C5/C9 copolymer resin by using peracetic acid.
Background
Petroleum resins are thermoplastic resins produced by polymerizing a C5 fraction and a C9 fraction among ethylene cracking byproducts, and are generally classified into: aliphatic hydrocarbon resins (C5), aliphatic hydrocarbon-aromatic hydrocarbon resins (C5/C9), aromatic hydrocarbon resins (C9) and dicyclopentadiene resins (DCPD). Wherein, because the raw materials in the C5/C9 copolymer resin contain naphthalene, dicyclopentadiene, methylcyclopentadiene dimer and the like, more double bonds and aromatic hydrocarbon groups are still remained in the molecule after the copolymer resin is polymerized into the resin, so that the copolymer resin has the defects of large smell, poor thermal stability and the like, and the further application of the copolymer resin is limited.
Disclosure of Invention
The technical problem to be solved by the invention is to provide a method for modifying C5/C9 copolymerized resin by using peracetic acid (PAA), wherein the method induces C5/C9 copolymerized petroleum resin to generate ring-opening reaction by adding PAA as an initiator, so that the unsaturation degree of the resin is reduced, and further the smell of the resin is reduced.
The invention provides a method for modifying C5/C9 copolymer resin by using peracetic acid, which comprises the following steps:
(1) uniformly mixing the C5 and C9 fractions according to the mass ratio of 1 (0.1-9.0) to obtain a polymerization raw material; adding a solvent into a reactor with stirring in advance, then uniformly dropwise adding the polymerization raw materials and the catalyst respectively, wherein the feeding time is 1.0-2.0 h, the reaction temperature is-10-30 ℃, and then carrying out heat preservation reaction at 20-50 ℃ for 0.5-2.0 h to obtain a polymerization solution;
(2) adding excessive sodium hydroxide solution into the polymerization solution at 35-70 ℃, carrying out alkali washing to remove the catalyst, washing with clear water to neutrality, and then carrying out steam stripping to remove unreacted raw materials and solvent at 220-250 ℃ and under 105-130 kPa to obtain molten resin solution;
(3) and stirring and mixing the molten resin liquid and peroxyacetic acid at 80-150 ℃ for 3-30 min in a double-screw stirring extruder to obtain the modified C5/C9 copolymer resin.
The solvent in the step (1) is one or more of cyclohexane, methylcyclohexane, toluene, xylene, petroleum ether, mineral oil and white oil, and the addition amount of the solvent is 30-50 wt% of the total mass of the materials.
The catalyst in the step (1) is Freidel-Crafts catalyst, and the addition amount of the catalyst is 0.2-2 wt% of the total mass of the materials.
The Freidel-Crafts catalyst is one of gaseous boron trifluoride, a boron trifluoride complex, anhydrous ferric trichloride and anhydrous aluminum trichloride.
The medium selected for stripping in the step (2) is one or more of methane, ethane and propane.
The addition amount of the peroxyacetic acid in the step (3) is 0.5-5.0 wt% of the mass of the molten resin liquid.
The softening point of the modified C5/C9 copolymer resin obtained in the step (3) is 90-130 ℃, the odor score is less than or equal to 3.0, and the content of VOCs is less than or equal to 1.5 wt%.
Advantageous effects
(1) The method has the advantages that peroxyacetic acid is added as an initiator to induce C5/C9 copolymerized petroleum resin to generate ring-opening reaction, so that the unsaturation degree of the petroleum resin product is reduced, and the odor of the resin is reduced; meanwhile, the method has low cost, simple process and good application prospect;
(2) the invention preferably adopts methane as a stripping medium, improves the effect of removing resin solvent and oligomer, reduces resin VOCs, and further reduces resin odor.
Detailed Description
The invention will be further illustrated with reference to the following specific examples. It should be understood that these examples are for illustrative purposes only and are not intended to limit the scope of the present invention. Further, it should be understood that various changes or modifications of the present invention may be made by those skilled in the art after reading the teaching of the present invention, and such equivalents may fall within the scope of the present invention as defined in the appended claims.
Cracking C5 fraction composition main compound composition
Components Content (a) of Components Content (a) of
1-butene + isobutene 0.49 2-methyl-2-butene 1.74
1, 3-butadiene 1.22 Trans-1, 3-pentadiene 20.02
N-butane 0.03 Cyclopentadiene 10.78
Trans-butene-2 0.19 Cyclopentene 14.92
Cis-buten-2 0.23 Cyclopentane 3.39
2-methyl-butane 2.16 2, 3-dimethylbutane 0.76
1, 2-butadiene 0.07 2-methylpentane 0.19
3-methyl-1-butene 0.85 2-methyl-1-pentene 0.27
Isoprene (I)Alkane (I) and its preparation method 1.64 N-hexane 0.87
1, 4-pentadienes 2.71 Methylcyclopentane 0.79
2-butyne 0.94 Benzene and its derivatives 0.76
1-pentene 6.13 Dicyclopentadiene 6.11
2-methyl-butene-1 4.27 Heavy fraction 2.50
N-pentane 4.52 Unknown substance 2.43
Isoprene (I) 4.34
Trans-2-pentene 2.85
Ethylene byproduct C9 fraction main compound composition
Serial number Name of Compound Content (a) of Serial number Name of Compound Content (a) of
1 Cyclopentadiene 0.75 17 Diethyl-1, 3-xylene 1.54
2 1-methylcyclopentadiene 0.87 18 Bicyclo [2, 2 ]]Oct-2-ene 4.62
3 Spiro [2, 4 ]]-hepta-4, 6-diene 0.20 19 4-ethylene-1, 2-xylene 1.99
4 Ethylbenzene production 0.13 20 1-ethylene-2, 3-xylene 0.43
5 Para-xylene 0.82 21 1, 2, 4, 5-tetramethylbenzene 1.00
6 Ortho-and meta-xylene 3.29 22 1-ethylene-2, 4-xylene 1.06
7 Cyclopropyl benzene 7.28 23 2, 4-Dimethylstyrene 0.97
8 Propyl benzene 0.68 24 4-vinyl-1, 2-xylene 0.31
9 1-methyl-2-toluene 4.56 25 2-ethylene-1, 4-xylene 0.20
10 Trimethylbenzene 2.68 26 1, 3-dimethyl-5-toluene 0.30
11 α -Methylstyrene 2.71 27 2-methylindene 3.26
12 1-vinyl-3-toluene 13.15 28 1-methyl-1-hydroindene 2.31
13 Dicyclopentadiene 11.08 29 Naphthalene 5.37
14 Indene 7.29 30 Dodecane 0.53
15 Tetraethyl-1, 2-xylene 1.52 31 2-methylnaphthalene 0.44
16 1-methyl-2-propylbenzene 0.32
Petroleum resin odor test method:
with reference to the german automobile industry association standard VDA 270(1992EN) requirements for odor emission of automotive interior parts, the odor test method and evaluation rating of petroleum resin are specified as follows:
putting 1.0 +/-0.05 g of resin into a 250mL closed container, baking at the temperature of 80 +/-2 ℃ for 2h +/-2 min, cooling to room temperature, and performing odor evaluation on 3 testers respectively. The evaluation grade is 1-6 grades, the minimum evaluation unit is 0.5, and the final test result is obtained by 3 scoring and averaging.
The specific criteria are as follows:
Figure BDA0002589925020000031
example 1
Uniformly mixing C5 and C9 fractions according to the mass ratio of 1:7 to obtain a polymerization raw material, firstly putting dimethylbenzene accounting for 45% of the total mass of the raw material as a solvent in a reactor with a stirrer, then uniformly dropwise adding the polymerization raw material and a boron trifluoride diethyl etherate catalyst accounting for 1.0% of the total mass of the raw material respectively, wherein the feeding time is 1.0h, the reaction temperature is 0 ℃ when dropwise adding, and then carrying out heat preservation reaction at 25 ℃ for 1.0h to obtain a polymerization solution. The resin liquid is washed by excessive 10 percent sodium hydroxide solution at 65 ℃ to remove a catalyst, then washed by clean water to be neutral, and stripped by taking methane as a medium at 230 ℃ and 115kPa to remove unreacted raw materials and solvent, so as to obtain the molten resin liquid with the softening point of 103.2 ℃, the color number of 4.7#, the odor score of 5.5 and the VOCs content of 6.85 percent.
And stirring and mixing the molten resin liquid and 0.8 wt% of PAA for 5min at 95 ℃ in a double-screw stirring extruder to obtain the modified C5/C9 copolymer resin with the softening point of 107.2 ℃, the color number of 4.9#, the odor score of 2.5 and the VOCs content of 3.50%.
Examples 2 to 6
Examples 2 to 6 are resin properties comparisons obtained under different modification conditions using the molten resin prepared by the method of example 1 and having a softening point of 103.2 ℃, a color number of 4.7#, an odor score of 5.5, and a VOCs content of 6.85%.
Figure BDA0002589925020000041
From the above examples, it is understood that when the amount of PAA used is increased and the reaction time is prolonged, the softening point and the weight average molecular weight Mw of the modified copolymer resin can be significantly increased, but the color number of the resin is easily deteriorated. An increase in the reaction temperature is advantageous for reducing the odor of the resin and the content of VOCs, but at the same time leads to a deepening of the color number of the resin and an increase in the weight-average molecular weight Mw.
The liquid of the C5/C9 copolymer resin before modification has heavy smell, and the modified resin still has no irritant smell.
Example 7
Uniformly mixing C5 and C9 fractions according to the mass ratio of 1: 0.1 to obtain a polymerization raw material, firstly putting dimethylbenzene accounting for 40% of the total mass of the materials as a solvent in a reactor with a stirrer, then uniformly dropwise adding the polymerization raw material and a boron trifluoride diethyl etherate catalyst accounting for 1.0% of the total mass of the materials respectively, wherein the feeding time is 1.0h, the reaction temperature is 0 ℃ during dropwise adding, and then carrying out heat preservation reaction at 25 ℃ for 1.0h to obtain a polymerization liquid. The resin liquid is washed by excessive 10 percent sodium hydroxide solution at 65 ℃ to remove a catalyst, then washed by clean water to be neutral, and stripped by taking methane as a medium at 230 ℃ and 115kPa to remove unreacted raw materials and solvent, so as to obtain the molten resin liquid with the softening point of 98.7 ℃, the color number of 3.3#, the odor score of 3.7 and the VOCs content of 3.56%.
In a double-screw stirring extruder, the molten resin liquid and 1.5 percent of PAA are stirred and mixed for 5min at 125 ℃ to obtain the modified C5/C9 copolymer resin with the softening point of 102.2 ℃, the color number of 3.5#, the odor score of 1.5 and the VOCs content of 1.89 percent.
Example 8
Uniformly mixing C5 and C9 fractions according to the mass ratio of 1: 1 to obtain a polymerization raw material, firstly putting dimethylbenzene accounting for 40 percent of the total mass of the raw material as a solvent in a reactor with a stirrer, then uniformly dropwise adding the polymerization raw material and a boron trifluoride diethyl etherate catalyst accounting for 0.8 percent of the total mass of the raw material respectively, wherein the feeding time is 1.0h, the reaction temperature is 0 ℃ when dropwise adding, and then carrying out heat preservation reaction at 35 ℃ for 2.0h to obtain a polymerization solution. The resin liquid is washed by excessive 10 percent sodium hydroxide solution at 65 ℃ to remove a catalyst, then washed by clean water to be neutral, and stripped by taking ethane as a medium at 250 ℃ and under the pressure of 105kPa to remove unreacted raw materials and solvent, so as to obtain the molten resin liquid with the softening point of 101.0 ℃, the color number of 4.0#, the odor score of 4.5 and the VOCs content of 2.26%.
In a double-screw stirring extruder, the molten resin liquid and 1.0% PAA are stirred and mixed for 10min at 120 ℃ to obtain the modified C5/C9 copolymer resin with the softening point of 104.4 ℃, the color number of 4.5#, the odor score of 2.0 and the VOCs content of 1.50%.

Claims (7)

1. A method of modifying a C5/C9 copolymer resin with peroxyacetic acid, comprising:
(1) uniformly mixing the C5 and C9 fractions according to the mass ratio of 1 (0.1-9.0) to obtain a polymerization raw material; adding a solvent into a reactor with stirring in advance, then uniformly dropwise adding the polymerization raw materials and the catalyst respectively, wherein the feeding time is 1.0-2.0 h, the reaction temperature is-10-30 ℃, and then carrying out heat preservation reaction at 20-50 ℃ for 0.5-2.0 h to obtain a polymerization solution;
(2) adding excessive sodium hydroxide solution into the polymerization solution at 35-70 ℃, carrying out alkali washing to remove the catalyst, washing with clear water to neutrality, and then carrying out steam stripping to remove unreacted raw materials and solvent at 220-250 ℃ and under 105-130 kPa to obtain molten resin solution;
(3) and stirring and mixing the molten resin liquid and peroxyacetic acid at 80-150 ℃ for 3-30 min in a double-screw stirring extruder to obtain the modified C5/C9 copolymer resin.
2. The method of claim 1, wherein: the solvent in the step (1) is one or more of cyclohexane, methylcyclohexane, toluene, xylene, petroleum ether, mineral oil and white oil, and the addition amount of the solvent is 30-50 wt% of the total mass of the materials.
3. The method of claim 1, wherein: the catalyst in the step (1) is Freidel-Crafts catalyst, and the addition amount of the catalyst is 0.2-2 wt% of the total mass of the materials.
4. The method of claim 3, wherein: the Freidel-Crafts catalyst is one of gaseous boron trifluoride, a boron trifluoride complex, anhydrous ferric trichloride and anhydrous aluminum trichloride.
5. The method of claim 1, wherein: the medium selected for stripping in the step (2) is one or more of methane, ethane and propane.
6. The method of claim 1, wherein: the addition amount of the peroxyacetic acid in the step (3) is 0.5-5.0 wt% of the mass of the molten resin liquid.
7. The method of claim 1, wherein: the softening point of the modified C5/C9 copolymer resin obtained in the step (3) is 90-130 ℃, the odor score is less than or equal to 3.0, and the content of VOCs is less than or equal to 1.5 wt%.
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112851858A (en) * 2021-01-13 2021-05-28 淄博鲁华泓锦新材料股份有限公司 C5 petroleum resin takes off system of urging

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CN103772610A (en) * 2012-10-24 2014-05-07 中国石油化工股份有限公司 Oxidation decolouring refining method of C5 / C9 petroleum resin
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US20200010595A1 (en) * 2017-03-08 2020-01-09 Exxonmobil Chemical Patents Inc. Polar Functionalized Hydrocarbon Resin Via Post-Reactor Modification

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112851858A (en) * 2021-01-13 2021-05-28 淄博鲁华泓锦新材料股份有限公司 C5 petroleum resin takes off system of urging
CN112851858B (en) * 2021-01-13 2022-09-16 淄博鲁华泓锦新材料集团股份有限公司 C5 petroleum resin takes off system of urging

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