WO2007111403A1

WO2007111403A1 - Dispersant for manufacturing vinyl chloride resin and method of manufacturing vinyl chloride resin using the same

Info

Publication number: WO2007111403A1
Application number: PCT/KR2006/003311
Authority: WO
Inventors: Yi-Rac Choi; Kyung-Hyun Kim; Seong-Yong Ahn; Min-Ju Yi; Hyun-Kyou Ha
Original assignee: LG Chem Ltd
Current assignee: LG Chem Ltd
Priority date: 2006-03-29
Filing date: 2006-08-23
Publication date: 2007-10-04
Anticipated expiration: 2008-09-29
Also published as: EP1881998A1; CA2581727A1; US20070232771A1; CN101133087A; JP2008520821A; EP1881998A4; KR20070097742A; TW200736279A

Abstract

The present invention relates to a dispersant for manufacturing vinyl chloride resin and a method of manufacturing vinyl chloride resin using the same. More precisely, this invention relates to a dispersant which is prepared by RAFT, harbors a hydrophobic group and one or more hydrophilic groups not containing a hydroxy group, and has a polydispersity index of 1.1 - 2, and a method of manufacturing vinyl chloride resin using the said dispersant. The dispersant for manufacturing vinyl chloride resin of the present invention and the manufacturing method of the present invention facilitates the preparation of vinyl chloride resin characterized by even size distribution, excellent sphericity and proper particle diameter.

Description

DISPERSANT FOR MANUFACTURING VINYL CHLORIDE RESIN AND

METHOD OF MANUFACTURING VINYL CHLORIDE

RESIN USING THE SAME

[Technical Field]

The present invention relates to a dispersant for

manufacturing vinyl chloride resin and a method of

manufacturing vinyl chloride resin using the same. More

precisely, the present invention relates to a dispersant

for manufacturing vinyl chloride resin which is

characterized by even size distribution, excellent

sphericity and proper particle diameter and a method of

manufacturing vinyl chloride resin using the same.

[Background Art]

In general, a dispersant is added to the reaction

solution when manufacturing a vinyl chloride resin by

suspension polymerization, aiming at dispersing various

reactants including monomers. At this time, a dispersant

has to have properly regulated hydrophilicity/hydrophobicity and regular molecular

weight, since these dispersant characteristics

significantly affect the particle size, size distribution

and the stability of a final vinyl chloride resin product ,

A dispersant itself is a polymer. Ion

polymerization is a conventional method to produce a

polymer having a narrow molecular weight distribution but

applicable monomers are limited and reaction conditions

are very strict, making this method industrially

inapplicable.

So, another attempt has been made to prepare a

polymer with a narrow molecular weight distribution,

which is living free radical polymerization. The reaction

conditions for this method are simple compared with those

of ion polymerization, thereby increasing industrial

applicability. According to living free radical

polymerization, the molecular weight distribution can be

regulated easily owing to the quick initiation reaction,

and the chain activity is preserved during the

polymerization, which is the living property, because the reversible exchange reaction between active species and

dormant ..species is induced continuously. In addition,'

the selection of a monomer and the polymerization

conditions are not strictly limited, enabling the

synthesis of such polymers as block copolymers having

different structures .

For living free radical polymerization, various

reaction methods such as iniferter method, nitroxide

method, ATRP (atom transfer radical polymerization) and

RAFT (reversible addition-fragmentation chain transfer

polymerization) have been proposed.

According to the conventional method for

manufacturing vinyl chloride resin, a hydrophobic monomer

is polymerized first and then a dispersant with some of

the hydroxy groups (-0H) substituted to increase

hydrophilicity, or a cellulose dispersant is added

thereto. However, such dispersants exhibit a cloud point

within the polymerization temperature range, resulting in

a precipitate which will decrease the colloid stability.

As a result, the properties such as size distribution and sphericity of the final vinyl chloride resin product

decrease.

WO 97/08212 describes a polymerization method using

a dispersant having a hydrophilic group and a hydrophobic

group. However, in this method, a dispersant is simply

obtained by solution polymerization, resulting in a

dispersant with a wide molecular weight distribution.

Such a dispersant with a wide molecular weight

distribution also reduces the properties, including

granularity, of the final polymer product.

Thus, it has long been the aim to produce a

dispersant with regular size distribution, excellent

sphericity and proper average particle diameter for use

in preparing vinyl chloride resin, but this has not yet

been achieved.

[Disclosure of the Invention]

It is an object of the present invention to provide

a method of manufacturing vinyl chloride resin which is

characterized by even size distribution, excellent sphericity and proper particle diameter.

It is another object of the present invention to

provide a dispersant useful for the above manufacturing

method.

The above objects of the present invention and

other additional objects can be achieved by the exemplary

embodiments of the present invention described in detail

hereinafter.

To achieve the first object, the present invention

provides a method of manufacturing vinyl chloride resin

including the step of suspension polymerization after

dispersing 100 weight part of vinyl chloride monomer;

0.01 - 1 weight part of a dispersant harboring a

hydrophobic group and one or more hydrophilic groups not

containing a hydroxy group and having a polydispersity

index of 1.1 - 2; and 0.01 - 1 weight part of an

initiator in a solvent.

The hydrophilic group is preferably one of C3 - C₇

carboxylic acid, C₂ - C₉ sulfonic acid or C₂ - Cg hydroxy

group. Particularly, the carboxylic acid is selected from a group consisting of acrylic acid, methacrylic acid,

itaconic acid and maleic* anhydride. The sulfonic acid

can be styrene sulfonic acid. The alcohol used above is

hydroxyethylacrylate, hydroxyethylmethacrylate or

ethyleneglycolmonovinylether .

The hydrophobic monomer is selected from a group

consisting of vinylacetate, ethylacetate, methylacrylate,

ethylacrylate, 2-ethylhexylacrylate, butylmethacrylate,

butylacrylate, methylmethacrylate and

glycidylmethacrylate .

It is also preferred that the molar ratio of the

hydrophilic group to hydrophobic group in the dispersant

is 5:5 - 8:2.

The method of manufacturing vinyl chloride resin of

the present invention facilitates the production of vinyl

chloride resin having regular size distribution,

excellent sphericity and proper particle diameter.

To achieve the second object of the present

invention, the present invention provides a dispersant

for manufacturing vinyl chloride resin, in which both a hydrophilic group and hydrophobic group are included, the

molar ratio of the hydrophilic group to hydrophobic group

is 5:5 - 8:2 and the hydrophilic group harbors one or

more hydrophilic groups which are not a hydroxy group but

might be C₃ - C₇ carboxylic acid, C₂ - C₉ sulfonic acid or

C₂ - C₉ hydroxy group.

The polydispersity index of the above dispersant is

preferably 1.1 - 2.

The present invention is described in detail

hereinafter .

The present invention provides a method of

manufacturing vinyl chloride resin including the step of

suspension polymerization after dispersing 100 weight

part of vinyl chloride monomer; 0.01 - 1 weight part of a

dispersant harboring a hydrophobic group and one or more

hydrophilic groups not containing a hydroxy group and

having a polydispersity index of 1.1 - 2; and 0.01 - 1

weight part of an initiator in a solvent.

As explained hereinbefore, a dispersant itself is a polymer which plays a role in dispersing various

reactants including a"monoπιer in a solvent as a droplet.

The monomer and the solvent are formed in two phases and

various reactants including a monomer are suspended in

the solvent. At this time, a dispersant including both a

hydrophilic group and a hydrophobic group reduces the

surface tension of the droplet. The present inventors

confirmed that the dispersant of the invention is very

useful for manufacturing vinyl chloride resin with

regular size distribution, excellent sphericity and

proper diameter.

The hydrophilic group of the dispersant is

preferably one of C₃ - C₇ carboxylic acid, C₂ - Cg

sulfonic acid or C₂ - C₉ hydroxy group. Particularly, the

carboxylic acid is selected from a group consisting of

acrylic acid, methacrylic acid, itaconic acid and maleic

anhydride. The sulfonic acid can be styrene sulfonic

acid. The hydroxy group can be hydroxyethylacrylate,

hydroxyethylmethacrylate or ethyleneglycolmonovinylether .

The hydrophobic group of the dispersant is selected from a group consisting of vinylacetate, ethylacetate,

methylacrylate, ethylacrylate, 2-ethylhexylacrylate,

butylmethacrylate, butylacrylate, methylmethacrylate and

glycidylmethacrylate .

The carbon number of the hydrophobic group is

preferably 4 - 9 but is not always limited thereto.

It is preferred that the molar ratio of the

hydrophilic group to hydrophobic group in the dispersant

is 5:5 - 8:2. When the hydrophilic group is less than

the above ratio range, the activity as a protective

colloid on the interface of water and vinyl chloride

monomer is weakened, reducing significantly the stability

of a particle. On the contrary, when the hydrophilic

group is over the above .ratio range of 8:2, the primary

particles in vinyl chloride monomer droplets are easily

aggregated, decreasing porosity.

The dispersant herein is prepared by the following

processes; regulating the molar ratio of hydrophilic

monomers to hydrophobic monomers to 5:5 - 8:2; mixing 100

weight part of the mixture of hydrophilic monomers and hydrophobic monomers with 0.01 - 1 weight part of an

initiator and 0.-01 - 5 weight part of a chain transfer

agent; and polymerizing the reaction mixture by RAFT

(reversible addition-fragmentation chain transfer

polymerization) .

The hydrophilic monomer used for preparing the

dispersant is selected from a group consisting of C₃ - C₇

carboxylic acid, C₂ - Cg sulfonic acid and C₂ - Cg alcohol.

Particularly, the carboxylic acid is selected from a

group consisting of acrylic acid, methacrylic acid,

itaconic acid and maleic anhydride. The sulfonic acid

can be styrene sulfonic acid. The alcohol can be

hydroxyethylacrylate, hydroxyethylmethacrylate or

ethyleneglycolmonovinylether .

The hydrophobic monomer used for preparing the

dispersant can be selected from a group consisting of

vinylacetate, ethylacetate, methylacrylate,, ethylacrylate,

2-ethylhexylacrylate, butylmethacrylate, butylacrylate,

methylmethacrylate and glycidylmethacrylate .

The initiator used for preparing the dispersant is selected from a group consisting of

azobisdiisobutyronitrile (AIBN) , benzoyl peroxide (BPO) ,

methylethylketone peroxide, diacethyl peroxide, lauryl

peroxide and tertiary butyl peroxide, but is not always

limited thereto. The preferable content of the initiator

in the dispersant is 0.01 - 1 weight part for the 100

weight part of the monomer. Less than 0.01 weight part

of content of the initiator results in the decrease of

polymerization speed thus prolonging the reaction time,

so that the level of non-reacted monomers increases. On

the contrary, more than 1 weight part of the initiator

content causes the molecular weight to decrease and the

molecular weight distribution to increase.

The chain transfer agent used for preparing the

dispersant of the present invention is involved in the

regulation of the molecular weight and molecular weight

distribution of the dispersant according to the value of

the shift constant. Also, a dithioester chain transfer

agent can be used. The preferable content of the chain

transfer agent in the dispersant is 0.01 - 5 weight part for 100 weight part of the monomer. Less than 0.01

weight part of the chain transfer agent content reduces

the capability of regulating the molecular weight

distribution. On the contrary, more than 5 weight part

of the chain transfer agent content reduces the

polymerization speed.

The polymerization of the dispersant is performed

by RAFT (reversible addition-fragmentation chain transfer

polymerization) at 40 - 100°C for 4 - 48 hours. During

RAFT the active species and propagating species interact

with each other by reversible polymerization or

depolymerization mediated by the chain transfer agent to

grow continuously, suggesting a living property. Because

of the living property, it produces a polymer with a

narrow molecular weight distribution. It is also able to

produce a block copolymer or a polymer with high

molecular weight by adding a monomer.

The dispersant prepared by RAFT has a narrow

molecular weight distribution and the early ratio of

hydrophilic monomers to hydrophobic monomers is consistent with that of the final polymer.

The molecular weight distribution of the dispersant

can be explained by the polydispersity index. The

polydispersity index is obtained by dividing the weight

average molecular weight of a polymer by the number mean

molecular weight. The wider the molecular weight

distribution, the higher the polydispersity index goes.

The narrower the molecular weight distribution, the

^• closer the polydispersity index is to 1.. It is

preferable that the polydispersity index of the

dispersant of the invention be 1.1 - 2. A dispersant

with a polydispersity index less than 1.1 is difficult to

manufacture and a dispersant with a polydispersity index

higher than 2 is not fully functional for preparing vinyl

chloride resin.

The preferable content of the dispersant is 0.001 -

1 weight part for 100 weight part of vinyl chloride

monomer. When the content of the dispersant is less than

0.01 weight part, the activity as a protective colloid on

the interface of water and vinyl chloride decreases, causing a problem of over-sized particles. When the

content ^'of the dispersant is more than 1 weight part, the

average diameter is smaller and the content of non-

reacted molecules is higher.

Any conventional initiator available for radical

polymerization can be used for manufacturing vinyl

chloride resin, which is exemplified by AIBN, BPO,

methylethylketone peroxide, diacethyl peroxide, lauryl

peroxide and tertiary butyl peroxide, but is not always

limited thereto. The preferable content of the initiator

is 0.01 - 1 weight part for 100 weight part of vinyl

chloride monomer. When the content of the initiator is

less than 0.01 weight part, polymerization speed is

reduced, making reaction time longer, and the content of

non-reacted molecules is higher. When the content of the

initiator is more than 1 weight part, the excessive

initiator reduces thermo-stability and alters the color

of the final resin product.

A solvent is used herein to disperse reactants

rather than to dissolve them, and water can be used as a solvent but is not always limited thereto. Any liquid

that is able to form two phases with a monomer to make a

suspension can be utilized, for example de-ionized water,

etc.

Suspension polymerization is preferably used for

the polymerization of vinyl chloride resin. According to

this method, impurities such as oxygen, etc, are

eliminated from the reactor and a solvent, an initiator

and a dispersant are added together and then vinyl

chloride monomer is added thereto. The reaction

temperature is raised. When it reaches a desired level,

the temperature is maintained at the level and reaction

is induced with stirring at regular speed to disperse the

droplet properly.

Upon completion of the reaction, remaining non-

reacted vinyl chloride is recovered. The resin product

in the reactor is dried to give vinyl chloride resin.

The suspension polymerization above is one

exemplary embodiment of the present invention, however

this does not limit the spirit and scope of the present invention .

[Brief Description of the Drawings]

The above and other objects, features and

advantages of the present invention will become apparent

from the following description of preferred embodiments

given in conjunction with the accompanying drawings, in

which:

Fig. 1 is a photograph illustrating the particles

of vinyl chloride resin prepared by the manufacturing

method of the present invention in Example 3.

Fig. 2 is a photograph illustrating the particles

of vinyl chloride resin prepared by the manufacturing

method of the present invention in Example 4.

Fig. 3 is a photograph illustrating the particles

of vinyl chloride resin prepared by the manufacturing

method of the present invention in Comparative Example 1.

[Best Modes for Carrying out the Invention]

Practical and presently preferred embodiments of the present invention are illustrated as shown in the

following examples .

However, it will be appreciated that those skilled

in the art, on consideration of this disclosure, may make

modifications and improvements within the spirit and

scope of the present invention.

The physical properties of the vinyl chloride resin

have been evaluated as follows.

Polydispersity index

GPC (gel permeation chromatography) was performed

with the prepared dispersant to evaluate the weight

average molecular weight and the number mean molecular

weight. After determining the ratio of the two, the

polydispersity index was calculated. For GPC of the

present invention, Waters HPLC (Waters) was used.

<Example 1> Preparation of a dispersant by RAFT

polymerization

To a 3-neck flask were added 20 mL of methylmethacrylate, 0.027 g of the initiator N, N-

azobisisobutyronitrile (AIBN) and 0.021 g of benzyl

dithiobenzoate, then 50 ml of benzene was added thereto

as a solvent. Reaction was induced at 60^°C for 4 hours

in the presence of nitrogen. Upon completion of the

reaction, the pressure was reduced and monomers and the

solvent were evaporated.

The prepared polymethylmethacrylate was dissolved

in 20 mL of dimethylformamide, to which 5 mL of acrylic

acid and 0.015 g of AIBN were added, followed by reaction

at 60 "C for 4 hours. Then, the solvent was evaporated to

give a dispersant in the form of a block copolymer. The

polydispersity index of the dispersant was 1.25.

<Example 2> Preparation of a dispersant by RAFT

polymerization

To a 3-neck flask were added 20 mL of

butylmethacrylate, 0.027 g of the initiator N, N-

azobisisobutyronitrile (AIBN) and 0.021 g of benzyl

dithiobenzoate, then 50 ml of benzene was added thereto as a solvent. Reaction was induced at 60^°C for 4 hours

in the presence of nitrogen. Upon completion of the

reaction, the pressure was reduced and monomers and the

solvent were evaporated.

The prepared polymethylmethacrylate was dissolved

in 20 mL of dimethylformamide, to which 5 mL of acrylic

acid and 0.015 g of AIBN were added, followed by reaction

at 60 °C for 4 hours. Then, the solvent was evaporated to

give a dispersant in the form of a block copolymer. The

polydispersity index of the dispersant was 1.88.

<Example 3> Preparation of vinyl chloride resin

using the dispersant prepared in Example 1

To a 1000 liter reactor were added 130 weight part

of de-ionized water, 0.06 weight part of the dispersant

prepared in Example 1 and 0.06 weight part of the

initiator bis (2-ethylhexyl) peroxydicarbonate for 100

weight part of vinyl chloride monomer together at the

same time, followed by stirring in a vacuum. After

adding vinyl chloride monomers, the reaction temperature was raised to 58 ^°C , followed by polymerization. When the

pressure of the reactor reached 7 kg/cm², the reactor was

cooled down and non-reacted vinyl chloride monomers were

recovered. The included water was eliminated and the

product was dried.

<Example 4> Preparation of vinyl chloride resin

using the dispersant prepared in Example 2

To a 1000 liter reactor were added 130 weight part

of de-ionized water, 0.06 weight part of the dispersant

prepared in Example 2 and 0.06 weight part of the

initiator bis (2-ethylhexyl)peroxydicarbonate for 100

weight part of vinyl chloride monomer together at the

same time, followed by stirring in a vacuum. After

adding vinyl chloride monomers, the reaction temperature

was raised to 58 °C, followed by polymerization. When the

pressure of the reactor reached 7 kg/cm², the reactor was

cooled down and non-reacted vinyl chloride monomers were

recovered. The included water was eliminated and the

product was dried. <Comparative Example 1> Preparation of vinyl

chloride resin using partially saponified vinyl acetate

resin

To a 1000 liter reactor were added 130 weight part

of de-ionized water, 0.06 weight part of a cellulose

dispersant and 0.06 weight part of the initiator bis (2-

ethylhexyl) peroxydicarbonate for 100 weight part of vinyl

chloride monomer together at .the same time, followed by

stirring in a vacuum. After adding vinyl chloride

monomers, the reaction temperature was raised to 58 "C,

followed by polymerization. When the pressure of the

reactor reached 7 kg/cm², the reactor was cooled down and

non-reacted vinyl chloride monomers were recovered. The

included water was eliminated and the product was dried.

The vinyl chloride polymers prepared in Examples 3

and 4 and Comparative Example 1 were tested to determine

the average diameter of particles and size distribution

by using mastersizer (Malvern) . The results are shown in

Table 1. The vinyl chloride polymers prepared in Examples 3 and 4 and Comparative Example 1 were

photographed, as shown in Figures 1, 2 and 3.

[Table 1]

As shown in Table 1, the average diameter of vinyl

chloride resin particles manufactured by using the

dispersant of the present invention prepared by RAFT was

a little smaller than that of the vinyl chloride resin of

Comparative Example 1. From the result, it was presumed

that the resins of Examples 3 and 4 might have better

plasticity than the resin of Comparative Example 1.

The size distributions of the resins of Examples 3

and 4 were respectively 0.63 and 0.59, which are narrower

than the size distribution of the resin of Comparative

Example 1 (0.82), suggesting that the resins of Examples

3 and 4 have more regular distributions .

The size distributions of the resins of Figs. 1 and

2 were observed to be very even, compared with that of Fig . 3 .

[industrial Applicability)

The dispersant for manufacturing vinyl chloride

resin of the present invention and the method of

manufacturing vinyl chloride resin using the dispersant

of the present invention enables the preparation of vinyl

chloride resin with even size distribution, excellent

sphericity and proper particle diameter.

Those skilled in the art will appreciate that the

conceptions and specific embodiments disclosed in the

foregoing description may be readily utilized as a basis

for modifying or designing other embodiments for carrying

out the same purposes as the present invention. Those

skilled in the art will also appreciate that such

equivalent embodiments do not depart from the spirit and

scope of the invention as set forth in the appended

claims .

Claims

[CLAIMS]

[Claim 1]

A method of manufacturing vinyl chloride resin

including the step of suspension polymerization in which

100 weight part of vinyl chloride monomer; 0.01 - 1

weight part of a dispersant having a hydrophobic group

and one or more hydrophilic groups not containing a

hydroxy group, with a polydispersity index of 1.1 - 2;

and 0.01 - 1 weight part of an initiator are dispersed in

a solvent .

[Claim 2]

The method of manufacturing vinyl chloride resin

according to claim 1, wherein the hydrophilic group is C₃

- C₇ carboxylic acid or C₂ - C₉ sulfonic acid.

[Claim 3]

The method of manufacturing vinyl chloride resin

according to claim 2, wherein the carboxylic acid is

selected from a group consisting of acrylic acid, methacrylic acid, itaconic acid and maleic anhydride.

[Claim 4]

The method of manufacturing vinyl chloride resin

according to claim 2, wherein the sulfonic acid is

styrene sulfonic acid.

[Claim 5]

The method of manufacturing vinyl chloride resin

according to claim 1, wherein the hydrophobic monomer

harboring a hydrophobic group is selected from a group

consisting of vinylacetate, ethylacetate, methylacrylate,

ethylacrylate, 2-ethylhexylacrylate, butylmethacrylate,

butylacrylate, methylmethacrylate and

glycidylmethacrylate.

[Claim β]

The method of manufacturing vinyl chloride resin

according to claim 1, wherein the molar ratio of the

hydrophilic group to the hydrophobic group in the dispersant is 5:5 - 8:2.

[Claim 7]

The method of manufacturing vinyl chloride resin

according to claim I₁ wherein the dispersant is prepared

by RAFT (reversible addition-fragmentation chain transfer

polymerization) with 100 weight part of the monomer

mixture of the hydrophilic monomers and hydrophobic

monomers wherein the molar ratio of the hydrophilic group

to the hydrophobic group is 5:5 - 8:2, 0.01 - 1 weight

part of an initiator and 0.01 - 5 weight part of a chain

transfer agent.

[Claim 8]

The method of manufacturing vinyl chloride resin

according to claim 7, wherein the chain transfer agent is

a dithioester.

[Claim 9]

The method of manufacturing vinyl chloride resin according to claim 7, wherein the polymerization of the

dispersant is performed at 40 - 100^°C.

[Claim lθ]

A dispersant for manufacturing vinyl chloride resin,

wherein a hydrophilic group and a hydrophobic group are

included at the molar ratio of 5:5 - 8:2, and the

hydrophilic group contains one or more hydrophilic groups

but not a hydroxy group and is either C₃ - C₇ carboxylic

acid or C₂ - C₉ sulfonic acid.

[Claim 11]

The dispersant for manufacturing vinyl chloride

resin according to claim 10, wherein the polydispersity

index of the dispersant for manufacturing vinyl chloride

resin is 1.1 - 2.