WO2000068304A1 - Preparation de particules polymeres de nanoencapsulation contenant des creux - Google Patents

Preparation de particules polymeres de nanoencapsulation contenant des creux Download PDF

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Publication number
WO2000068304A1
WO2000068304A1 PCT/FI2000/000371 FI0000371W WO0068304A1 WO 2000068304 A1 WO2000068304 A1 WO 2000068304A1 FI 0000371 W FI0000371 W FI 0000371W WO 0068304 A1 WO0068304 A1 WO 0068304A1
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core
shell
monomer
stage
particles
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PCT/FI2000/000371
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English (en)
Inventor
Valery Pavlyuchenko
Sergey Ivanchev
Olga Sorochinskaya
Mikael Skrifvars
Jukka Koskinen
Hanna Laamanen
Toivo Kärnä
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Neste Chemicals Oy
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Priority to AU42995/00A priority Critical patent/AU4299500A/en
Priority to EP00922681A priority patent/EP1098927A1/fr
Publication of WO2000068304A1 publication Critical patent/WO2000068304A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F285/00—Macromolecular compounds obtained by polymerising monomers on to preformed graft polymers

Definitions

  • the present invention relates to a process for preparing with core-shell particles containing microvoids by emulsion polymerization. More specifically, the present invention relates to a process for preparing emulsion polymers which comprise an internal layer with an alkali - swellable resin, earring out a subsequential emulsion polymerization to form a hard polymer layer outside the internal layer, swelling the internal layer with an alkali or more exact volatile base such as ammonia or amine and then drying to remove water contained in the alkali-swellable resin, thereby forming a microvoid in the center of polymer particle.
  • emulsion polymers which comprise an internal layer with an alkali - swellable resin, earring out a subsequential emulsion polymerization to form a hard polymer layer outside the internal layer, swelling the internal layer with an alkali or more exact volatile base such as ammonia or amine and then drying to remove water contained in the alkali-swellable resin, thereby forming
  • Polymer particles containing voids are useful as opacifying agents in coating applications such as paint or paper coating, particularly for high quality paper products where colour pictures are presented, such as art books, brochures, magazines etc.
  • the use of microvoid containing polymer particles reduces or removes the need for inorganic pigments, such as titanium dioxide, or extenders, without adding excessive and undesirable weight to coating.
  • Microvoid containing polymer particles have found extensive applications as white plastic pigments and they have started to replace the earlier used polymers filled uniformly in particles.
  • US 4 973 670 discloses a process for preparing polymer particles containing microvoids by a two step emulsion polymerization.
  • the first step involves introducing of an organic phase to an aqueous phase.
  • the organic phase comprises monomer which is insoluble in the aqueous phase and water insoluble hydrocarbon.
  • the monomer is polymerized to produce a low molecular weight polymer such that the polymer will phase separate from organic phase and concentrates at the surface of the introduced organic phase.
  • the second step is an additional polymerization of a crosslinking monomer with the low molecular weight polymer to produce microvoid containing particles.
  • the main drawback of the process is a necessity to remove the hydrocarbon by stripping.
  • US 5 360 827 discloses a process for preparation of polymer particles containing microvoids which are prepared by adding a base in the presence of a monomer to a latex containing copolymer particles modified carboxylic to make the pH of the latex 8 or more, and by adding monomers containing carboxyl group to make pH of the latex 7 or less and then by polymerizing these monomers.
  • This process leaves high amounts of residual monomers in the product and thus an additional steam distillation operation is required.
  • a structure of the particles prepared is rather indefinite. As a rule each particle contains several voids.
  • US 5 578 650 discloses a process for emulsification of (meth)acrylate ester in the presence of water and at least one acid that is not free radically polymerizable and an emulsifier followed by (meth)acrylic ester polymerization to produce microspheres, a majority of which have cavities that upon drying become voids. Similar to the process according to US 5 360 827 each particle contains as a rule several voids. Moreover particles are too high in size to provide good opacifying ability.
  • a number of processes for making polymer particles containing microvoids based on an application of core-shell particles as precursors of the polymer particles are known. These processes provide a preparation of polymer particles containing microvoid of more definite structure, namely a single microvoid in the center of a polymer particle. In addition said processes have suitable particle size, usually 0.1-2.0 mm. for opacifying.
  • US 4 427 836 discloses a process for making core-shell polymer particles containing microvoids, comprising (A) emulsion polymerization a core from a core monomer system comprised at least one ethylenically unsaturated acid monomer; (B) encapsulating said core with a hard shell by emulsion polymerization a shell monomer system in the presence of said core; (C) neutralizing with ammonia or amine so as to swell said core and form particles which, when dried, contain a single void. According to the process at least one additional shell can be polymerized subsequent to step (C).
  • the process has several disadvantages.
  • the first one is in that the stability of latex is poor, particularly at stage (A) due to polarity and hydrophilicity of highly carboxylated core and low adso ⁇ tion energy of a surfactant. That is why a lot of coagulate is formed during this stage.
  • the second disadvantage consists in that the conditions of particle swelling and their expansion are not suitable enough particularly when glass transition temperature (Tg) of a shell polymer is higher than 100°C. e.g. Tg of poly(methyl methacrylate) is 105°C. According to examples of US patent No. 4,427.836 temperature of neutralization does not exceed 95°C. The situation with the conditions of particle swelling can be improved.
  • US 4 594 363 discloses a process for making core-shell polymer particles containing voids comprising emulsion polymerizing a core from a core monomer system comprised of at least one ethylenically unsaturated monomer containing acid functionally encapsulating said core with a hard sheath by emulsion polymerizing a shell monomer system in the presence of said core and swelling at elevated temperature the resultant core-shell polymer particles with fixed or permanent base in the presence of solvent.
  • the solvent decreases Tg of the shell polymer and alleviates the swelling.
  • the main drawback of the process is a presence of organic solvent in the final polymer dispersion. Besides, the problems with the latex stability during highly carboxylated core preparation remain to be solved.
  • US 4 970 241 discloses multi-stage polymer particles containing one or more void space(s) which are produced by sequential emulsion polymerization of an essentially low-acid earlier polymer stage, encapsulation of said low-acid polymer stage with at least a final polymer stage, contacting said polymer particles with a non-polymeric carboxylic acid or anhydride to be absorbed into said low-acid polymer stage and swelling the polymer particles by contacting the particles with an aqueous base at a temperature near or above the Tg of the polymer.
  • US 5 157 084 discloses a process of making polymer particles containing microvoids also without the use of acid in the swellable polymer core.
  • a swellability of the polymer core at elevated temperature is achieved by inco ⁇ oration into the core polymer (meth)acrylate ester units which are hydrolyzable in alkaline environments.
  • the drawback of the process is too high temperature of the hydrolysis process (up to 150°C). Thus the process must be performed under pressure. Besides usually problems with latex stability arise at such severe conditions.
  • the present invention comprises a process for making core-shell polymer particles containing voids, said particles useful for opacifying. comprising (A) emulsion 0 polymerization a core from a core monomer system comprised of ethylenically unsaturated monomer containing acid functionality; (B) encapsulating said core with a hard shell by emulsion polymerizing a shell monomer system in the presence of said core, and (C) swelling at elevated temperature the resultant core-shell polymer particles with volatile base so as to produce an aqueous dispersion of particles which when dried contain a 5 microvoid which causes opacity in compositions in which they are contained, characterized in that
  • (1) core monomer system comprises from about 50.0% by weight to about 79.9% by weight, based on the total weight of the core monomer system, of (meth)acrylic ester from about 20.0% by weight to about 40% by weight, based on the total weight of the core o monomer system unsaturated carboxylic acid, from about 0.1 % by weight to about 1.0% by weight, based on the total weight of the core monomer system, and optionally from about 5% by weight to 15% weight, based on the total weight of the core monomer system of crosslinking monomer, of vinyl aromatic monomer.;
  • stage (C) carried out at the temperature higher than glass transition temperature of the 0 system of shell polymer-shell monomers added at stage (C) is followed by (D) polymerization of shell monomers charged at stage (C).
  • Stages (A) and (B) are carried out at continuous feeding of all of the components as two flows, the first one comprising the monomer mixture and the second one comprising the aqueous solution of initiator and surfactant.
  • the invention comprises latex compositions comprising core-shell polymer particles prepared by the said process and coatings which are produced with the compositions.
  • All polymerization stages of the process are carried out as semi-continuous emulsion polymerization stages.
  • Emulsion polymerization is carried out in the presence of water- soluble free radical initiators such as sodium, potassium or ammonium persulphate and anionic surfactants such as sodium dodecyl benzene sulphonate. sodium alkyl sulphonate. sodium lauryl sulphate at a temperature from 70°C to 95 °C.
  • Semicontinuous polymerizations are carried out at continuous feeding of the components. This approach has a number of advantages.
  • a constant feeding of an initiator provides high rate of polymerization so that "monomer starvation" conditions are realized and a kinetic steric barrier is arisen. It means correct core-shell mo ⁇ hology is formed without any phase inversion even if hard hydrophobic shell is formed onto hydrophilic core.
  • a constant feeding of a surfactant allows to carry out polymerization onto seed particles only, i.e. without formation of new particles. It's very important particularly for stage (B) because formation of new particles at this stage means the occurrence of the particles free of carboxylated core which are not able to swell in the presence of base at stage (C).
  • a constant feeding of all of the components reduces a coagulate formation during the polymerization.
  • the core polymer is the product of aqueous emulsion copolymerization of (meth)acrylic ester, unsaturated carboxylic acid, cross-linking monomer and optionally vinyl aromatic monomer.
  • Suitable (meth)acrylic esters include methyl methacrylate, ethyl methacrylate, butyl(meth)acrylate, 2-ethylhexyl (meth)acrylate.
  • Suitable unsaturated carboxylic acids include acrylic acid and methacrylic acid, which are preferred, and itaconic acid, maleic acid or anhydride and monomethyl maleate or monomethyl itaconate.
  • the cross-linking monomer is meant to include monomers conventionally known in the art as useful for preparation of crosslinked polymers. Examples of such monomers typically include di- and trifunctional monomers having two or three unsaturated bonds such as divinyl benzene. ethylene glycol diacrylate. ethylene glycol dimethacrylate.
  • the acid-containing core polymer may be obtained also by a process involving a stage of seed latex preparation.
  • the seed latex is prepared by emulsion copolymerization of 96.0- 99.5 weight parts, preferably 97.0-98.5 weight parts of (meth)acrylic esters with 0.5-4.0 weight parts, preferably 1.5-3.0 weight parts of unsaturated carboxylic acid as a batch process.
  • the amounts of components at seed step are as follows: 100 weight parts of distilled water, 1.0-4.0 weight parts, preferably 2.0-3.0 weight parts of monomers, 0.04-0.5 weight parts, preferably 0.1-0.3 weight parts of initiator and 0.001-0.040 weight parts, preferably 0.005-0.015 weight parts of anionic surfactant.
  • the seed particles may have an average size in the range of 70 to 100 nm diameter.
  • Said ratios of the components provide a stable core polymer latex preparation with low content of coagulate (less than 3.5 wt-%).
  • Average particle size depending on the selected ratio of the components is in the range of 140 to 320 nm. More preferable average particle size is from 200 nm to 220 nm.
  • the core polymer latex is unsaturated one with a surfactant due to surface tension is in the range of 39 to 50 mN/m. Hence a correct choice of the surfactant concentration at stage (B) excludes'a formation of new particles.
  • the present inventors have found that incorporation of vinyl aromatic monomer units into the core polymer provides the preparation of core polymer latex completely free of coagulate.
  • a subsequent stage of emulsion polymerization is effected to form a shell polymer on the acid core polymer particles. This may be performed in the same reaction vessel in which the formation of the core was accomplished or the reaction medium containing the dispersed core particles may be transferred to another reaction container.
  • the shell monomer system comprises vinyl aromatic monomer and/or (meth)acrylic esters.
  • the shell monomer system may or may not contain a small amount of acid component (no more than 3.0%) by the weight of the total amount of the shell monomers).
  • the shell monomer system may or may not contain a crosslinking monomer.
  • Stage (B) may or may not comprise two or more steps with various monomer compositions.
  • 0.3-4.0 weight parts based on 100 weight parts of the shell monomers preferably 0.8-2.0 weight parts of initiator and 0.1-1.5 weight parts based on 100 weight parts of the shell monomers, preferably 0.4-0.8 weight parts of surfactant are used. These amounts and feeding of components provide high rate of polymerization (monomer starvation conditions) and permit to avoid the occurrence of new particles.
  • the diameter of core-shell particles is in the range from 250 to 800 nm.
  • the weight ratio of core polymer to shell polymer is from 1 :4 to 1 :40. preferably from 1 :6 to 1 :20.
  • Tg stage (C) Swelling of the core-shell particles at stage (C) with volatile base are to be carried out at a temperature higher compared to Tg of shell polymer. Under such kind of conditions only one may expect an adequate swelling and expansion of the particles. As a rule Tg of the hard shell polymer is above 100°C. That is why even an application of elevated temperatures (85-95°C) at stage (C) is not enough.
  • Tg stage (C) is performed in the presence of a monomer or monomer mixture. To prevent polymerization of the monomers charged at stage (C) a radical inhibitor is added simultaneously. When the swelling of the particles is completed an additional amount of initiator is charged into the reaction system and added monomers are polymerized.
  • the final polymer dispersion does not contain any organic low molecular weight admixtures.
  • US 4 594 363 indicates that the swelling can be carried out in the presence of the shell monomer system.
  • the swelling of the particles is not effective enough when the radical inhibitor is absent due to monomers added at stage (C) are polymerized quickly at elevated temperature.
  • the monomers at stage (C) can be added before, after, or with the addition of the ⁇ olatile base.
  • a nonionic surfactant is added before the swelling to prevent a partial coagulation of the polymer dispersion.
  • the shell monomer system is applied at stage (C) as a component Tg reducing.
  • other monomers compatible with core-shell polymer can be used, e.g. crosslinking monomers to increase Tg and hardness of the final product.
  • Suitable amounts of the monomers added at stage (C) are about 1 -40 parts by weight, based on 100 parts by weight core-shell polymer, preferably 5-15 parts by weight.
  • K.Adachi et al. in their study published in J. Polymer Sci., Polymer Phys.Ed., v.13. No. 1 1.
  • p. 2155-2171 (1975) show that addition from 5 to 10 weight parts of low molecular weight organic solvent per 100 weight parts of polystyrene reduces Tg up to 60-80°C.
  • Suitable radical inhibitors are well-known effective acceptors of free radicals such as benzoquinone, hydroquinone. nitrobenzene, trinitrobenzene, stable radicals such as diphenylpicryl hydrozyl, nitroxy radicals etc.
  • the amount of the radical inhibitor depending on the amounts of the monomers added at stage (C) is in the range from 0.01 to 0.40 parts by weight, based on 100 parts by weight core-shell polymer, preferably 0.05-0.15 parts by weight.
  • Nonionic surfactant such as ethoxylated aliphatic alcohol or alkyl phenol depending on the amounts of the monomers added at stage (C) is used in amounts of 0.02 to 1.2 parts by weight, based on 100 parts by weight core-shell polymer, preferably 0.1-0.5 parts by weight.
  • Volatile bases such as ammonia or volatile organic bases, such as trimethyl amine, triethyl amine or diethyl ethanol amine are used as suitable swelling agents in amounts of 1.0-1.5 equivalents per 1 equivalent of carboxy-groups inco ⁇ orated into the core-shell polymer. Due to elevated temperature (85-95°C) at the swelling procedure the stage (C) is carried out in the closed reactor under a small pressure (no more than 0.5 kg/cm2) in order to prevent a volatile base loss because non-controlled loss of the volatile base deteriorates the process reproducibility. When the swelling procedure is completed an additional amount of initiator (0.5-1.0 parts by weight, based on 100 parts by weight monomers added at stage (C) is charged to polymerize said monomers (stage D).
  • initiator 0.5-1.0 parts by weight, based on 100 parts by weight monomers added at stage (C) is charged to polymerize said monomers (stage D).
  • An optional stage (E) comprises preparation of an additional shell with elevated Tg or vice versa with reduced Tg to prepare film forming polymer dispersion.
  • vinyl aromatic monomers and/or (meth)acrylic esters are used.
  • Crosslinking monomers may or may not be used.
  • the conditions of stage (E) are practically the same as those at stage (B).
  • the resulting polymer dispersions obtained according to the present invention depending on the ratios of the components and the reaction conditions have the following properties: - solids 25-40 wt-%
  • the multistage core-shell polymer dispersions of the present invention are useful for aqueous coating compositions as opacifying agents either as a supplement to, or replacement of, pigmentary matter and/or extenders therefore.
  • the aqueous dispersions of the core-shell polymer may be added directly to the waterborn coating compositions.
  • the gloss of the coatings prepared on the basis of said coating compositions can be controlled by the composition of the core polymer. It turns out when the core polymer contains vinyl aromatic monomer units the coatings prepared are glossy. When the core polymer is free of vinyl aromatic units the coatings prepared are nonglossy or mat.
  • the opacifying ability of the core-shell polymer particles containing voids obtained according to the present invention is defined as a contrast ratio of the coatings prepared with a film forming polymer dispersion and said core-shell polymer particles.
  • the contrast ratio is determined by photometric method 4 to 5 glass plates are coated with a coating composition (film forming latex of styrene-n-butyl acrylate-methacrylic acid 37:58:5 wt-% + said core-shell polymer dispersion).
  • the process is carried out in 250 ml flask equipped with stirrer. reflux condenser, inlet for nitrogen and necks for feeding components.
  • the feed is fulfilled with syringe pumps.
  • MMA Methyl methacrylate
  • BA n-Butyl acrylate
  • SDBS Sodium dodecylbenzene sulphonate
  • This step is carried out as a batch process. 45.0 g of distilled water is charged into the flask and heated up to 82°C with stirring and nitrogen flow. Then SDBS solution is charged. In 5 min. PP solution and monomer mixture 1 are added. The process period (after the monomer mixture charge) is 1 hour. Average particle size of seed particles is 90 nm.
  • Seed latex prepared at step 1 Monomer mixture 2 (composition is varied, see table 1 ) 33.00 g SDBS (20.8% aqueous solution), amount varied, see table 1 PP 0.166 g Distilled water 96.00 g
  • Step 2 starts straight away after completing step 1.
  • the monomer mixture 2 and aqueous phase are simultaneously fed into the seed latex within 3 hours. Then the process continues for another 20 min. followed by cooling, discharging and filtering of the latex prepared.
  • the properties of the latexes prepared depending on the monomer mixture 2 composition and SDBS amount are listed in table 1.
  • EGDM is ethylene glycol dimethacrylate, MMA methyl methacrylate.
  • Table 1 illustrates that styrene inco ⁇ oration into the monomer mixture 2 almost completely eliminates the coagulate formation.
  • the Shell is Polystyrene.
  • Latex of the core polymer prepared according to one of the embodiments of example 1 is Latex of Latex of the core polymer prepared according to one of the embodiments of example 1
  • Aqueous phase for feed PP 0.73 g
  • Latex of core-shell polymer and distilled water are charged into the flask.
  • the flask content is heated in the nitrogen flow up to 85°C, then aqueous solution of PP is added followed by feeding styrene and aqueous phase via syringe pumps. Feeding is carried out for 130 min. 0
  • Core-shell polymer latex prepared at stage B Ammonia aqueous solution (cone. 10.4% wt.) 4.76 g ST 9.39 g 2,2,6.6 - tetramethyl-4-oxo-pyperidin-oxyl-l (TEMPO) 0.177 g Disponil APE 257* aqueous solution (cone. 18.1% wt.) 5.32 g
  • Stage D Polymerization of styrene added at stage C.
  • aqueous latex blend of the following composition was prepared (weight parts): core-shell particles containing voids 3.0 film forming polymer 7.0 water 23.3
  • This latex blend was used for coatings preparation and evaluation of opacifying ability (R) and gloss.
  • Table 2 illustrates that excluding both monomer and inhibitor at neutralization stage deteriorates opacifying ability of core-shell particles containing voids significantly (examples 2C. 2D and 2E).
  • Table 2 illustrates that excluding both monomer and inhibitor at neutralization stage deteriorates opacifying ability of core-shell particles containing voids significantly (examples 2C. 2D and 2E).
  • Besides a composition of the core polymer is a very important factor providing a gloss control of the coatings prepared.
  • the core polymer contains ST units the coatings are glossy (example 2A and 2C).
  • the core polymer is free of ST units the coatings are mat (examples 2B, 2D and 2E).
  • the Shell is MMA-MAA Copolymer.
  • Example 2 Generally the procedure of Example 2 is used to prepare core-shell particles. However a recipe is distinguished and benzoquinone is used instead of TEMPO.
  • Stage B MMA-MAA copolymer shell preparation.
  • Latex of the core polymer prepared according to example 1 A 24.89 g MMA 24.28 g MAA 0 49 g PP 0.19 g Distilled water 128.0 g
  • Aqueous phase for feed :
  • a feeding of MMA and aqueous phase is carried out for 102 min.
  • Stage C Neutralization and swelling of the core-shell particles.
  • Ammonia aqueous solution (cone. 12.4% wt.) 3.2 g
  • Disponil APE 257 aqueous solution (cone. 18.1%) wt.) 3.32 g
  • Stage D Polymerization of MMA and MAA added at stage C.
  • the final diluted latex was examined with an electron microscope. A single void can be observed inside of each particle.
  • the procedure of the coating preparation is the same as in example 2.
  • the properties of the polymer dispersions and the coatings are listed in table 3.
  • Table 3 illustrates that elimination of inhibitor (example 3B) deteriorates opacifying ability.
  • the coatings are mat due to the core nolymer used (example 1A) does not contain ST units.
  • Example 3 Generally the procedure of Example 3 is used. However a recipe is distinguished.
  • Latex of the core polymer prepared according to example 1 A 26.36 g Monomer mixture 1 : MMA 10.39 g ST 8.41 g
  • Aqueous phase for feed PP 0.276 g
  • a feeding of the monomer mixture 1 and aqueous phase is carried out for 108 min.
  • Step 2 starts straight away after the completion of step 1.
  • Latex prepared at step 1 of the following monomer mixture 2 MMA 1.28 g
  • Aqueous phase for feed PP 0.187 g
  • a feeding of the monomer mixture 2 and aqueous phase is carried out for 73 min.
  • Stage C Neutralization and swelling of the core-shell particles.
  • Ammonia aqueous solution (cone. 12.4% wt.) 3.15 g
  • Stage D Polymerization of monomer mixture 2 added at stage C. Neutralized latex at stage C AP 0.19 g Distilled water 10.0 g
  • the final diluted latex was examined with an electron microscope. A single void can be observed inside of each particle.
  • the procedure of the coating preparation is the same as in example 2.
  • the properties of the polymer dispersions and the coatings are listed in table 4.
  • Table 4 illustrates that elimination of inhibitor (example 4B) deteriorates opacifying 0 ability.
  • the coatings are mat due to the core polymer used (example 1A) does not contain ST units.
  • Latex prepared according to example 4A 132.0 g o ST 23.17 g
  • the properties of the polymer dispersion and the coatings are as follows: Solids 35.0% wt.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
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  • Graft Or Block Polymers (AREA)

Abstract

L'invention concerne un procédé de production de particules polymères de nanoencapsulation contenant des creux consistant à polymériser en émulsion un noyau à partir d'un système noyau monomère constitué d'au moins un monomère insaturé à fonction acide éventuellement en présence de graines de latex, puis à encapsuler ce noyau avec une capsule dure par polymérisation en émulsion d'un système paroi monomère contenant au moins un ester vinylique aromatique et/ou carboxylique insaturé en présence de ce noyau et finalement à faire gonfler à une température élevée les particules polymères de nanoencapsulation obtenues avec une base volatile, les parois monomères, un inhibiteur de radical et un tensioactif non ionique. Les parois monomères chargées à l'étape de gonflement sont ensuite polymérisées pour obtenir une dispersion aqueuse de particules qui, une fois séchées, présentent des microcreux entraînant l'opacité des compositions. Les particules de nanoencapsulation ainsi obtenues sont utilisées dans les revêtements opaques et brillants.
PCT/FI2000/000371 1999-05-07 2000-04-28 Preparation de particules polymeres de nanoencapsulation contenant des creux WO2000068304A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
AU42995/00A AU4299500A (en) 1999-05-07 2000-04-28 Preparation of core-shell polymer particles containing voids
EP00922681A EP1098927A1 (fr) 1999-05-07 2000-04-28 Preparation de particules polymeres de nanoencapsulation contenant des creux

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FI991051A FI991051A (fi) 1999-05-07 1999-05-07 Huokosia sisältävien polymeerihiukkasten valmistamismenetelmä
FI991051 1999-05-07

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WO2007006766A1 (fr) * 2005-07-14 2007-01-18 Basf Aktiengesellschaft Procede de fabrication de polymerisats d'emulsion
EP1754730A1 (fr) 2005-08-19 2007-02-21 Rohm and Haas Company Dispersion aqueuse de particules polymériques.
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US8013081B2 (en) 2005-10-27 2011-09-06 Valspar Sourcing, Inc. Method for preparing polymer particles
EP2554609A2 (fr) 2011-08-05 2013-02-06 Rohm and Haas Company Composition de revêtement aqueux pour améliorer la résistance aux taches liquides
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US9303182B2 (en) 2012-06-05 2016-04-05 Dow Global Technologies Llc Aqueous coating composition with improved stability
WO2016172832A1 (fr) 2015-04-28 2016-11-03 Dow Global Technologies Llc Composition de peinture à faible lustre avec opacité efficace
US9546267B2 (en) 2012-09-17 2017-01-17 Rohm And Haas Company Multi-stage polymer as a grinding additive and a method of producing the same
WO2017012033A1 (fr) 2015-07-21 2017-01-26 Rohm And Haas Company Composition de revêtement aqueuse
CN106519125A (zh) * 2016-11-10 2017-03-22 无锡市明盛强力风机有限公司 一种核壳空心乳液的制备方法
CN106543373A (zh) * 2016-11-10 2017-03-29 无锡市明盛强力风机有限公司 一种软硬双层壳空心乳液的制备方法
WO2017100993A1 (fr) 2015-12-15 2017-06-22 Dow Global Technologies Llc Polymère à phases multiples utilisable en tant qu'additif de broyage et son procédé de production
US9816002B2 (en) 2012-10-12 2017-11-14 Dow Global Technologies Llc Aqueous coating composition with improved viscosity stability
WO2018040060A1 (fr) 2016-09-02 2018-03-08 Dow Global Technologies Llc Composition de revêtement présentant une résistance hydrophobe élevée et une résistance hydrophile élevée
US10550279B2 (en) 2014-06-30 2020-02-04 Dow Global Technologies Llc Antimicrobial coating composition with improved yellowing resistance
US11802173B2 (en) 2015-08-04 2023-10-31 Arkema Inc. Voided latex particles containing functionalized outer shells

Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4594363A (en) * 1985-01-11 1986-06-10 Rohm And Haas Company Production of core-sheath polymer particles containing voids, resulting product and use
US4970241A (en) * 1988-05-20 1990-11-13 Rohm And Haas Company Multi-stage opacifying polymer particles containing non-polymeric acid absorbed therein
US4973670A (en) * 1988-08-12 1990-11-27 The Dow Chemical Company Method for preparing hollow latexes
EP0404184A2 (fr) * 1989-06-23 1990-12-27 Nippon Zeon Co., Ltd. Procédé de préparation de particules polymères contenant des microcavités
EP0451940A2 (fr) * 1990-03-30 1991-10-16 Tioxide Group Limited Préparation de particules de polymère
US5157084A (en) * 1990-10-12 1992-10-20 The Dow Chemical Company Process of making hollow polymer latex particles
WO1994004603A1 (fr) * 1992-08-19 1994-03-03 The Dow Chemical Company Particules creuses de latex polymere
US5360827A (en) * 1992-03-31 1994-11-01 Nippon Zeon Co., Ltd. Process for preparation of latex of hollow polymer
WO1995011265A1 (fr) * 1993-10-20 1995-04-27 Lucky Ltd. Procede pour preparer des polymeres en emulsion presentant une structure creuse
US5639805A (en) * 1991-12-13 1997-06-17 Korea Chemical Co., Ltd. Process for preparing core-shell emulsion polymer particles and resulting product containing such particles
WO1998039372A1 (fr) * 1997-03-05 1998-09-11 Neste Chemicals Oy Procede de preparation d'un latex comprenant des particules polymeres creuses
WO1998055522A1 (fr) * 1997-06-05 1998-12-10 Neste Chemicals Oy Procede de preparation de copolymeres pour revetements polymeres antistatiques
EP0959176A1 (fr) * 1998-05-18 1999-11-24 Rohm And Haas Company Particules sphériques pigmentaires organiques pour papier ou pour le couchage du papier

Patent Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4594363A (en) * 1985-01-11 1986-06-10 Rohm And Haas Company Production of core-sheath polymer particles containing voids, resulting product and use
US4970241A (en) * 1988-05-20 1990-11-13 Rohm And Haas Company Multi-stage opacifying polymer particles containing non-polymeric acid absorbed therein
US4973670A (en) * 1988-08-12 1990-11-27 The Dow Chemical Company Method for preparing hollow latexes
EP0404184A2 (fr) * 1989-06-23 1990-12-27 Nippon Zeon Co., Ltd. Procédé de préparation de particules polymères contenant des microcavités
EP0451940A2 (fr) * 1990-03-30 1991-10-16 Tioxide Group Limited Préparation de particules de polymère
US5157084A (en) * 1990-10-12 1992-10-20 The Dow Chemical Company Process of making hollow polymer latex particles
US5639805A (en) * 1991-12-13 1997-06-17 Korea Chemical Co., Ltd. Process for preparing core-shell emulsion polymer particles and resulting product containing such particles
US5360827A (en) * 1992-03-31 1994-11-01 Nippon Zeon Co., Ltd. Process for preparation of latex of hollow polymer
WO1994004603A1 (fr) * 1992-08-19 1994-03-03 The Dow Chemical Company Particules creuses de latex polymere
WO1995011265A1 (fr) * 1993-10-20 1995-04-27 Lucky Ltd. Procede pour preparer des polymeres en emulsion presentant une structure creuse
WO1998039372A1 (fr) * 1997-03-05 1998-09-11 Neste Chemicals Oy Procede de preparation d'un latex comprenant des particules polymeres creuses
WO1998055522A1 (fr) * 1997-06-05 1998-12-10 Neste Chemicals Oy Procede de preparation de copolymeres pour revetements polymeres antistatiques
EP0959176A1 (fr) * 1998-05-18 1999-11-24 Rohm And Haas Company Particules sphériques pigmentaires organiques pour papier ou pour le couchage du papier

Cited By (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6673451B2 (en) 2000-10-12 2004-01-06 Rohn And Haas Company Process for forming an aqueous polymeric dispersion
EP1197503A3 (fr) * 2000-10-12 2003-05-21 Rohm And Haas Company Procédé de préparation de dispersions aqueuses de polymères
EP1710278A1 (fr) * 2004-01-26 2006-10-11 JSR Corporation Composition liquide contenant des particules creuses, son procede de production, et article optique
EP1710278A4 (fr) * 2004-01-26 2011-08-24 Jsr Corp Composition liquide contenant des particules creuses, son procede de production, et article optique
WO2005118732A1 (fr) * 2004-05-28 2005-12-15 Ecolab Inc. Finition pour sol, contenant un agent eclaircissant
CN1965043B (zh) * 2004-05-28 2013-04-10 埃科莱布有限公司 具有增亮剂的地面刷油
CN101223202B (zh) * 2005-07-14 2011-05-11 巴斯福股份公司 生产乳液聚合物的方法
WO2007006766A1 (fr) * 2005-07-14 2007-01-18 Basf Aktiengesellschaft Procede de fabrication de polymerisats d'emulsion
AU2006268625B2 (en) * 2005-07-14 2011-06-02 Basf Aktiengesellschaft Method for producing emulsion polymers
US7943704B2 (en) 2005-07-14 2011-05-17 Basf Aktiengesellschaft Method for producing emulsion polymers
KR100811519B1 (ko) 2005-08-19 2008-03-07 롬 앤드 하아스 컴패니 중합 입자의 수성 분산물
US8227542B2 (en) 2005-08-19 2012-07-24 Rohm And Haas Company Aqueous dispersion of polymeric particles
US7629414B2 (en) 2005-08-19 2009-12-08 Rohm And Haas Company Aqueous dispersion of polymeric particles
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AU2006203398B2 (en) * 2005-08-19 2011-09-29 Rohm And Haas Company Aqueous dispersion of polymeric particles
US8013081B2 (en) 2005-10-27 2011-09-06 Valspar Sourcing, Inc. Method for preparing polymer particles
US7645815B2 (en) 2007-01-16 2010-01-12 Rohm And Haas Company Fast-drying aqueous compositions with hollow particle binders and traffic paints made therewith
EP2072542A1 (fr) * 2007-12-20 2009-06-24 Rohm and Haas Company Polymère du type coeur-enveloppe et son utilisation dans les solutions organiques
US9102775B2 (en) 2007-12-20 2015-08-11 Rohm And Haas Company Core-shell polymers suitable for use in organic media
RU2506290C2 (ru) * 2007-12-20 2014-02-10 Ром Энд Хаас Компани Полимеры типа сердцевина/оболочка, приемлемые для применения в органических средах
AU2008252045B2 (en) * 2007-12-20 2013-06-20 Rohm And Haas Company Core-shell polymers suitable for use in organic media
EP2143742A1 (fr) * 2008-07-08 2010-01-13 Rohm and Haas Company Particules polymériques du type coeur-enveloppe.
US8445559B2 (en) 2008-07-08 2013-05-21 Rohm And Haas Company Core-shell polymeric particles
US20130210979A1 (en) * 2010-06-10 2013-08-15 Mitsubishi Rayon Co., Ltd Production method of acrylic polymer, acrylic polymer obtained by this production method and plastisol composition using the same
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EP2581392A1 (fr) * 2010-06-10 2013-04-17 Mitsubishi Rayon Co., Ltd. Procédé de production de polymère acrylique, polymère acrylique obtenu par le procédé, et composition de plastisol utilisant celui-ci
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