CN111732733A - Polyethyleneimine and polyether double-modified polyamide dendrimer compound and preparation method and application thereof - Google Patents

Polyethyleneimine and polyether double-modified polyamide dendrimer compound and preparation method and application thereof Download PDF

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CN111732733A
CN111732733A CN202010691739.7A CN202010691739A CN111732733A CN 111732733 A CN111732733 A CN 111732733A CN 202010691739 A CN202010691739 A CN 202010691739A CN 111732733 A CN111732733 A CN 111732733A
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polyether
dendrimer compound
acid
modified polyamide
ethyleneimine
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CN111732733B (en
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冉峰
王炳帅
王娟娟
王淼
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LIAONING KELONG FINE CHEMICAL CO Ltd
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LIAONING KELONG FINE CHEMICAL CO Ltd
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G81/00Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/46Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/06Paper forming aids
    • D21H21/10Retention agents or drainage improvers

Abstract

The invention discloses an ethylene imine and polyether double-modified polyamide dendrimer compound and a preparation method and application thereof. The dendrimer compound is prepared from aliphatic polyamide, ethylene imine and allyl polyether through Michael addition reaction. According to the prepared ethyleneimine and polyether double-modified polyamide dendrimer compound, the ethyleneimine and polyether groups are introduced into the main chain and the side chain of the polyamide, so that the characteristics of the polyamide are retained, and the anchoring property of the ethyleneimine and the hydrophilicity of the polyether are improved. The polyamide dendrimers obtained by the method can be used as retention aids for papermaking.

Description

Polyethyleneimine and polyether double-modified polyamide dendrimer compound and preparation method and application thereof
Technical Field
The invention belongs to the field of chemical synthesis, and particularly relates to a preparation method of an ethyleneimine and polyether double-modified polyamide dendrimer compound, in particular to an additive suitable for papermaking raw materials, such as a retention aid used in the papermaking industry.
Background
The polyamide dendrimer can be used as a retention aid in the papermaking industry because the polyamide dendrimer has a branch structure and can absorb fillers such as calcium carbonate. However, polyamide is hydrophobic, requires emulsification when used, and causes secondary pollution to pulp.
Disclosure of Invention
The invention aims to provide a preparation method of an ethylene imine and polyether double-modified polyamide dendrimer compound. According to the polyethyleneimine and polyether double-modified polyamide dendrimer compound prepared by the method, the polyethyleneimine and polyether groups are introduced into the polyamide structure, so that the polyamide dendrimer has hydrophilicity, and emulsification is not required during use.
In order to realize the purpose of the invention, the technical scheme adopted by the invention is as follows: an ethylene imine and polyether dual-modified polyamide dendrimer compound is prepared from aliphatic polyamide, ethylene imine and allyl polyether through Michael addition reaction in aqueous solution.
Further, the aliphatic polyamide is prepared from dihexyltriamine and a dicarboxylic acid through a polycondensation reaction.
Further, in the above-mentioned ethyleneimine and polyether double-modified polyamide dendrimer compound, the dibasic organic carboxylic acid is maleic acid, adipic acid, glutaric acid, malonic acid or sebacic acid.
Furthermore, in the above-mentioned polyimide and polyether double-modified polyamide dendrimer compound, the organic dicarboxylic acid is adipic acid.
Further, the above-mentioned ethyleneimine and polyether double-modified polyamide dendrimer compound, the allyl polyether has a structural formula shown in (I):
R-A-(EO)n-A-R (I)
wherein R is allyl or vinyl, A is-OCH2-or-CH2-EO is ethylene oxide units and n is 1-20.
Furthermore, in the above-mentioned polyimide and polyether double-modified polyamide dendrimer compound, R is vinyl, n is 8-14, and the allyl polyether has a structural formula shown in (ii);
Figure BDA0002589626030000011
a preparation method of an ethylene imine and polyether double-modified polyamide dendrimer compound comprises the following steps: adding aliphatic polyamide, distilled water and a catalyst into a reaction kettle in sequence, starting stirring, heating a reaction system to 80-90 ℃, dropwise adding an ethylene imine aqueous solution into the reaction system by using a constant flow pump, controlling the dropwise adding time to be 3-4 hours, preserving heat at 80-90 ℃ for 2 hours after the dropwise adding is finished, cooling the reaction system to 50-60 ℃, dropwise adding allyl polyether into the reaction system by using the constant flow pump, preserving heat at 50-60 ℃ for 30-40 minutes after the dropwise adding is finished, and cooling to obtain a target product.
Further, in the above preparation method, the catalyst is concentrated sulfuric acid, concentrated hydrochloric acid or acetic acid.
Further, in the above preparation method, the catalyst is concentrated sulfuric acid.
Further, in the above production method, the amount of the ethyleneimine added is 5 to 20 times the number of moles of the amine groups in the aliphatic polyamide.
Further, in the above production method, the amount of ethyleneimine added is 5 to 10 times the molar number of amine groups in the aliphatic polyamide
The invention relates to an application of an ethylene imine and polyether dual-modified polyamide dendrimer compound as a retention aid in the paper industry.
The invention has the beneficial effects that: according to the prepared ethylene imine and polyether dual-modified polyamide, the ethylene imine and polyether units are introduced into the main chain and the branched chain of the polyamide while the characteristics of the polyamide are kept, so that the polyamide has a dendritic structure and has the anchoring property of the ethylene imine, the polyether is introduced into the polyamide, the molecular weight of the polyamide can be further improved, the polyamide has the hydrophilicity of the polyether, and the hydrophobicity of the polyamide is improved. The prepared polyethyleneimine and polyether dual-modified polyamide dendrimer has both a hydrophobic group and a hydrophilic group, has anchoring property and high reactivity, and can be used as a retention aid in the paper industry. The method has simple preparation process and is easy to master.
Detailed Description
A preparation method of an ethylene imine and polyether double-modified polyamide dendrimer compound comprises the following steps: adding aliphatic polyamide, distilled water and a catalyst into a reaction kettle in sequence, starting stirring, heating a reaction system to 80-90 ℃, dropwise adding an ethylene imine aqueous solution into the reaction system by using a constant flow pump, controlling the dropwise adding time to be 3-4 hours, preserving heat at 80-90 ℃ for 2 hours after the dropwise adding is finished, cooling the reaction system to 50-60 ℃, dropwise adding allyl polyether into the reaction system by using the constant flow pump, preserving heat at 50-60 ℃ for 30-40 minutes after the dropwise adding is finished, and cooling to obtain a target product.
In the preparation method, the aliphatic polyamide is prepared by condensation polymerization of dihexyltriamine and a dibasic organic carboxylic acid, and the molar mass of the aliphatic polyamide is Mw (5000-. The dibasic organic carboxylic acid is maleic acid, adipic acid, glutaric acid, malonic acid or sebacic acid. Preferably, the dibasic organic carboxylic acid is adipic acid.
In the above preparation method, the addition amount of the ethylene imine is 5 to 20 times of the mole number of the amine groups in the aliphatic polyamide. Preferably, the molar addition amount of the ethylene imine is 5 to 10 times the molar number of the amine groups in the aliphatic polyamide.
In the preparation method, the catalyst is concentrated sulfuric acid, concentrated hydrochloric acid or acetic acid. Preferably, the catalyst is concentrated sulfuric acid.
In the above preparation method, the allyl polyether has a structural formula shown in (I):
R-A-(EO)n-A-R(I)
wherein R is allyl or vinyl, A is-OCH2-or-CH2-EO is ethylene oxide units and n is 1-20.
Preferably, R is vinyl, n is 8-14, and the allyl polyether has the formula shown in (ii):
Figure BDA0002589626030000031
example 1
Polyethyleneimine and polyether double-modified polyamide dendrimer compound-A1
The preparation method comprises the following steps
1. Preparation of aliphatic Polyamide having branched Structure-PA 1
Adding dihexyltriamine and deionized water into a reaction kettle according to the molar ratio of adipic acid to dihexyltriamine to deionized water of 1:1.1:3, wherein nitrogen protection is needed in the reaction process, adding adipic acid into the reaction kettle for 6 times at intervals of 30min every time, controlling the temperature of the reaction kettle not to exceed 70 ℃ in the process of adding adipic acid, and cooling by using circulating water if the temperature exceeds 70 ℃. And after the feeding is finished, heating for dehydration, controlling the reaction temperature at 170-140 ℃ for reaction for 8h, preserving the heat for 2h after the dehydration is finished, then cooling the reaction kettle to 130-140 ℃, slowly adding a certain amount of deionized water into the reaction kettle, uniformly stirring, discharging to obtain an aliphatic polyamide aqueous solution with the solid content of 60%, and recording as PA 1.
Mw was 8000 by GPC (reverse osmosis gel chromatography).
2. The structural formula of the polyether compound is as follows
Figure BDA0002589626030000032
Where n is 9 and Mw is 500, and is recorded as KLPG 5.
3. Preparation of ethyleneimine and polyether double-modified polyamide dendrimer compound
Adding 800g (amino content is 0.2mol) PA1, 160g distilled water and 10g concentrated sulfuric acid into a reaction kettle in sequence, starting stirring, heating the reaction system to 80-90 ℃, dropwise adding 160g of 50 wt% ethylene imine aqueous solution (ethylene imine content is 2mol) into the reaction system by using a constant flow pump, controlling the dropwise adding time to be 3-4 hours, and keeping the temperature at 80-90 ℃ for 2 hours after the dropwise adding is finished. And then cooling the reaction system to 50-60 ℃, dropwise adding 565g of 50 wt% KLPG5 aqueous solution into the reaction system by using a constant flow pump, preserving the temperature at 50-60 ℃ for 30 minutes after dropwise adding, cooling and discharging to obtain the polyethyleneimine and polyether double-modified polyamide dendrimer compound, which is marked as A1.
(II) detection
The weight average molecular weight (Mw) of the obtained product, namely the ethyleneimine and polyether double modified polyamide dendrimer compound A1 is 20000g/moL through GPC (reverse osmosis gel chromatography).
Example 2
Polyethyleneimine and polyether double-modified polyamide dendrimer compound-A2
The preparation method comprises the following steps:
1. preparation of aliphatic Polyamide having branched Structure-PA 1
The preparation method is the same as that of example 1
2. The structural formula of the polyether compound is as follows
Figure BDA0002589626030000041
Where n is 14 and Mw is 700, which is recorded as KLPG 7.
3. Preparation of ethyleneimine and polyether double-modified polyamide dendrimer compound
Adding 800g (amino content is 0.2mol) PA1, 160g distilled water and 10g concentrated sulfuric acid into a reaction kettle in sequence, starting stirring, heating the reaction system to 80-90 ℃, dropwise adding 160g of 50 wt% ethylene imine aqueous solution (ethylene imine content is 2mol) into the reaction system by using a constant flow pump, controlling the dropwise adding time to be 3-4 hours, and keeping the temperature at 80-90 ℃ for 2 hours after the dropwise adding is finished. And then cooling the reaction system to 50-60 ℃, dropwise adding 565g of 50 wt% KLPG7 aqueous solution into the reaction system by using a constant flow pump, preserving the temperature at 50-60 ℃ for 30 minutes after dropwise adding, cooling and discharging to obtain the polyethyleneimine and polyether double-modified polyamide dendrimer compound, which is marked as A2.
(II) detection
The weight average molecular weight (Mw) of the obtained product, namely the ethylene imine and polyether double modified polyamide dendrimer compound A2, is 40000g/moL according to GPC (reverse osmosis gel chromatography).
Example 3
Polyethyleneimine and polyether double-modified polyamide dendrimer compound-A3
The preparation method comprises the following steps:
1. preparation of aliphatic Polyamide having branched Structure-PA 1
The preparation method is the same as that of example 1
2. The structural formula of the polyether compound is as follows
Figure BDA0002589626030000042
Where n is 14 and Mw is 700, which is recorded as KLPG 7.
(III) preparing the ethyleneimine and polyether double-modified polyamide dendrimer compound
Adding 800g (amino content is 0.2mol) PA1, 160g distilled water and 10g concentrated sulfuric acid into a reaction kettle in sequence, starting stirring, heating the reaction system to 80-90 ℃, dropwise adding 160g of 50 wt% ethylene imine aqueous solution (ethylene imine content is 2mol) into the reaction system by using a constant flow pump, controlling the dropwise adding time to be 3-4 hours, and keeping the temperature at 80-90 ℃ for 2 hours after the dropwise adding is finished. And then cooling the reaction system to 50-60 ℃, dropwise adding 1130g of 50 wt% KLPG7 aqueous solution into the reaction system by using a constant flow pump, preserving the temperature at 50-60 ℃ for 30 minutes after dropwise adding, cooling and discharging to obtain the ethyleneimine and polyether double-modified polyamide dendrimer compound, which is recorded as A3.
(II) detection
The weight average molecular weight (Mw) of the obtained product, namely the ethylene imine and polyether double modified polyamide dendrimer compound A3, is 50000g/moL through GPC (reverse osmosis gel chromatography).
Example 4
The retention rates of the ethyleneimine and polyether double modified polyamide dendrimer compound A1-A3 prepared in examples 1-3 were measured by a dynamic drainage meter, and the results are shown in Table 1.
TABLE 1
Polymers of the examples Retention (%)
A1 88%
A2 91%
A3 90.5%
As can be seen from Table 1, the retention rate of the prepared ethyleneimine and polyether dual-modified polyamide dendrimer compound is 88-91%, and the compound can be used as an additive of papermaking raw materials, in particular as a retention aid in the papermaking industry.

Claims (10)

1. The polyimide and polyether double-modified polyamide dendrimer compound is characterized by being prepared from aliphatic polyamide, ethylene imine and allyl polyether through a Michael addition reaction in an aqueous solution.
2. The ethyleneimine and polyether double modified polyamide dendrimer compound as claimed in claim 1, wherein the aliphatic polyamide is prepared by polycondensation of diethylenetriamine and a dicarboxylic acid.
3. The compound of claim 2, wherein the organic dicarboxylic acid is maleic acid, adipic acid, glutaric acid, malonic acid, or sebacic acid.
4. The ethyleneimine and polyether double modified polyamide dendrimer compound of claim 3, wherein the organic dicarboxylic acid is adipic acid.
5. The ethyleneimine and polyether double modified polyamide dendrimer compound of claim 1, wherein the allyl polyether has a structural formula shown in formula (I):
R-A-(EO)n-A-R (I)
wherein R is allyl or vinyl, A is-OCH2-or-CH2-EO is ethylene oxide units and n is 1-20.
6. The ethyleneimine and polyether double modified polyamide dendrimer compound as claimed in claim 5, wherein R is vinyl, n is 8-14, and the allyl polyether has a structural formula shown as (II);
Figure FDA0002589626020000011
7. a preparation method of an ethylene imine and polyether double-modified polyamide dendrimer compound is characterized by comprising the following steps: adding aliphatic polyamide, distilled water and a catalyst into a reaction kettle in sequence, starting stirring, heating a reaction system to 80-90 ℃, dropwise adding an ethylene imine aqueous solution into the reaction system by using a constant flow pump, controlling the dropwise adding time to be 3-4 hours, preserving heat at 80-90 ℃ for 2 hours after the dropwise adding is finished, cooling the reaction system to 50-60 ℃, dropwise adding allyl polyether into the reaction system by using the constant flow pump, preserving heat at 50-60 ℃ for 30-40 minutes after the dropwise adding is finished, and cooling to obtain a target product.
8. The method according to claim 7, wherein the catalyst is concentrated sulfuric acid, concentrated hydrochloric acid, or acetic acid.
9. The process according to claim 7, wherein the amount of the ethyleneimine added is 5 to 20 times the number of moles of the amine groups in the aliphatic polyamide.
10. Use of an ethyleneimine and polyether double modified polyamide dendrimer compound according to any one of claims 1 to 6 as a retention aid in the paper industry.
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Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4144123A (en) * 1974-07-19 1979-03-13 Basf Aktiengesellschaft Incorporating a crosslinked polyamidoamine condensation product into paper-making pulp
CN1353625A (en) * 1999-05-10 2002-06-12 巴斯福股份公司 Method for fractionation of water soluble or dispersible polymers containing amino groups with broad molar mass distribution
CN101472966A (en) * 2006-05-18 2009-07-01 赫尔克里士公司 Michael addition adducts as additives for paper and papermaking
CN101492900A (en) * 2009-01-12 2009-07-29 山东轻工业学院 Retention aid and filtering aid of cation dendroid macromolecule for papermaking, preparation and uses thereof
CN103127525A (en) * 2013-02-27 2013-06-05 万礼 Tree-like polymer nanometer drug delivery carrier targeting doxorubicin and its preparation method
CN105735048A (en) * 2015-12-15 2016-07-06 广东省造纸研究所 High-permeability paper material and production process thereof
CN106543447A (en) * 2016-10-23 2017-03-29 中海油天津化工研究设计院有限公司 A kind of preparation method of hyper-branched type high water-content crude oil demulsifier
CN111100292A (en) * 2020-01-06 2020-05-05 辽宁科隆精细化工股份有限公司 Preparation method of high molecular weight branched polyethyleneimine

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4144123A (en) * 1974-07-19 1979-03-13 Basf Aktiengesellschaft Incorporating a crosslinked polyamidoamine condensation product into paper-making pulp
CN1353625A (en) * 1999-05-10 2002-06-12 巴斯福股份公司 Method for fractionation of water soluble or dispersible polymers containing amino groups with broad molar mass distribution
CN101472966A (en) * 2006-05-18 2009-07-01 赫尔克里士公司 Michael addition adducts as additives for paper and papermaking
CN101492900A (en) * 2009-01-12 2009-07-29 山东轻工业学院 Retention aid and filtering aid of cation dendroid macromolecule for papermaking, preparation and uses thereof
CN103127525A (en) * 2013-02-27 2013-06-05 万礼 Tree-like polymer nanometer drug delivery carrier targeting doxorubicin and its preparation method
CN105735048A (en) * 2015-12-15 2016-07-06 广东省造纸研究所 High-permeability paper material and production process thereof
CN106543447A (en) * 2016-10-23 2017-03-29 中海油天津化工研究设计院有限公司 A kind of preparation method of hyper-branched type high water-content crude oil demulsifier
CN111100292A (en) * 2020-01-06 2020-05-05 辽宁科隆精细化工股份有限公司 Preparation method of high molecular weight branched polyethyleneimine

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