WO2005100453A1 - Verfahren zur kontinuierlichen herstellung von siilicon emulsionen - Google Patents
Verfahren zur kontinuierlichen herstellung von siilicon emulsionen Download PDFInfo
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- WO2005100453A1 WO2005100453A1 PCT/EP2005/003960 EP2005003960W WO2005100453A1 WO 2005100453 A1 WO2005100453 A1 WO 2005100453A1 EP 2005003960 W EP2005003960 W EP 2005003960W WO 2005100453 A1 WO2005100453 A1 WO 2005100453A1
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- emulsifier
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/06—Preparatory processes
- C08G77/08—Preparatory processes characterised by the catalysts used
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2383/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
- C08J2383/04—Polysiloxanes
Definitions
- the invention relates to a process for the continuous production of aqueous silicone emulsions, wherein the
- Silicone emulsions are commercially available as milky white macro emulsions in the form of w / o or o / w emulsions and as opaque to transparent micro emulsions. They are mixtures of at least one water-insoluble silicone oil, resin or elastomer, at least one emulsifier and water. To prepare the emulsion, these components are made using e.g. Heat and cold, mechanical shear, by means of tight
- Columns can be generated in mixers, mixed together and dispersed.
- the silicone component of the emulsion can be prepared in an upstream reaction outside the emulsifying unit and then dispersed in the emulsifying unit. Or the silicone component of the emulsion can be produced in the emulsifying unit itself (in-situ production). It is characteristic of the in-situ production that a chemical reaction takes place shortly before, during or shortly after the emulsion production.
- Typical reactions for the in-situ production or polymerization of the silicone component are all reactions used in silicone chemistry that lead to chain extension or equilibration, such as polymerization, condensation or polyaddition reactions.
- the silicone is typically first mixed with at least one emulsifier and a small amount of water and subjected to high shear, for example in a rotor-stator mixer with narrow gaps. This typically results in a w / o emulsion with a very high viscosity, which is referred to as the so-called “rigid phase”. The viscosity of this rigid phase is very strongly dependent on the shear. This rigid phase is then slowly diluted with water to the inversion point The w / o becomes an o / w emulsion
- the formation of the rigid phase and the type of dilution with water to the desired final concentration of the emulsion determine the quality of the emulsion.
- the quality of the emulsion is understood to mean, in particular, the particle size, the distribution of the particle size, the storage stability and the tolerance of the emulsion to heating and / or cooling, shocks, changes in the pH value, changes in the salt content, etc.
- 17S 5 806 975 describes an apparatus and the method for emulsifying riochviscose silicones in an extruder-like device.
- US Pat. No. 5,563,189 claims the two-stage, continuous emulsion preparation, an emulsion with a high solids content being produced in the first stage, which is then diluted to the desired final concentration in a second shear device with additional water.
- EP 874 017 claims a method for producing silicone-in-water emulsions, at least one polysiloxane, another siloxane which reacts with the former by means of chain extension, and a metal catalyst therefor, and an emulsifier and water are continuously mixed and emulsified.
- WO 02/42360 describes the continuous production of emulsions by means of one or more shearing mixers, the siloxane, the emulsifier and the water being fed to the mixer through a line to form a rigid phase, and the pressure at the egg outlet of the mixer being kept constant at 20% becomes.
- the invention relates to a process for the continuous production of aqueous emulsions
- the pressure and the temperature after the high-shear mixers determine the quality of the emulsions of organosilicon compounds and that the quality of the emulsions produced can be significantly improved by the regulation.
- the regulation leads to microemulsions to clearer products with small particle sizes. Macro emulsions achieve significantly smaller particle sizes and improved storage and dilution stabilities. With the temperature control it is possible to control the particle sizes. This effect is supported by the pressure control.
- the pressure and temperature are regulated to a target value for the respective products.
- the pressure is preferably regulated by maintaining the pressure after the second high-shear mixer and by the speed or geometry of the high-shear mixer.
- the high shear mixers have a different delivery rate depending on the speed, which affects the pressure in the downstream line.
- the temperature is preferably regulated by the temperature of the
- Suitable high-shear mixers are, for example, rotor-stator mixers, high-speed stirrers / dissolvers, colloid mills, microchannels, membranes, high-pressure homogenizers and jet nozzles, in particular rotor-stator mixers.
- the pressures and temperatures after the mixers vary depending on the product and its viscosity.
- the pressures are preferably 1 to 10 bar.
- the temperatures are preferably 5 ° C to 100 ° C.
- the pressure and the temperature are preferably highest in or behind the first high-shear mixer which produces the highly viscous phase.
- At least 50, preferably at least 70% by weight of the organosilicon compound (A) is preferably mixed in the first high-shear mixer.
- the first high shear mixers are preferably admixed with at least 60, preferably at least 80% by weight of the emulsifier (B).
- Organosilicon compound (A), emulsifier (B) and water (C) e.g. supplied with continuously demanding pumps such as centrifugal pumps, gear pumps, rotary lobe pumps or rotary spindle pumps.
- pumps such as centrifugal pumps, gear pumps, rotary lobe pumps or rotary spindle pumps.
- emulsifier (B) and water (C) e.g. supplied with continuously demanding pumps such as centrifugal pumps, gear pumps, rotary lobe pumps or rotary spindle pumps.
- Another high shear mixer can be arranged in front of the first high shear mixer.
- further mixers preferably one or two mixers, can dilute the emulsion and make it ready.
- organosilicon compound (A), emulsifier (B) and water (C) can be added to the first or second high-shear mixer or incorporated in other mixers.
- Additives (Z) are preferably incorporated in the second high-shear mixer or in further mixers. It is also possible to add mixtures of (A), (B) and (C) and other additives (Z) to the first high-shear mixer, e.g. be premixed in a storage tank.
- the mixer can also be used to produce a pre-emulsion, solution or mixture of, for example, not completely water-soluble emulsifiers or thickeners with water.
- all silanes and organopolysiloxanes can be used as organosilicon compounds (A) and their mixtures, solutions or dispersions. Examples are linear organopolysiloxanes and silicone resins. Silicone resins are products that not only contain mono- and difunctional silicon units but also contain tri- and tetrafunctional silicon units.
- the emulsions prepared according to the invention have an organosilicon compound (A) content of at least 1% to 98%, preferably 5% to 90%, particularly preferably 9 to 80%.
- the particle sizes vary from 1 nm to 1000 ⁇ m, preferably from 5 nm to 300 ⁇ m, particularly preferably 10 nm to 200 ⁇ m.
- the pH values can vary from 1 to 14, preferably 2 to 10, particularly preferably 3 to 9.
- Organosilicon compound (A) is preferably liquid at 25 ° C. and preferably has viscosities of 0.5 to 500,000 mPa ⁇ s, in particular 2 to 80,000 mPa ⁇ s.
- organosilicon compounds are organosilicon compounds, the units of the general formula I. included, where
- R is a hydrogen atom or a monovalent, divalent or trivalent hydrocarbon radical having 1 to 200 carbon atoms, which can be substituted by halogen, amine, ammonium, mercapto, acrylate or maleimide groups
- X is a chlorine atom
- a radical of the formula -0 ⁇ with protons and / or organic or inorganic ionic substances may be present, a radical of the general formula -OR 1 or a radical of the general formula II - (R 2 ) h - [OCH 2 CH 2 ] e [0C 3 H 6 ] f [0C 4 H a ) 4 ]
- R 1 is a hydrogen atom or a hydrocarbon radical having 1 to 200 carbon atoms, which can be interrupted by one or more identical or different heteroatoms selected from 0, - S, N and P
- R 2 is a divalent hydrocarbon radical having 1 to 200 carbon atoms, which is represented by one or more groups of the formulas
- R 4 is a bivalent, trivalent or tetravalent hydrocarbon radical having 1 to 200 carbon atoms per radical, which is represented by one or more groups of the formulas -C (O) -, -C (0) 0-, - C (0) NR 5 , -NR 5 -, -N + HR S -, -N + R 5 R 5 -, -0-, -S-, - (HO) P (O) - or - (NaO) P (O) - interrupted and / or can be substituted by F, Cl or Br, where R s is a hydrogen atom or a hydrocarbon radical having 1 to 200 carbon atoms per radical, which is represented by one or more groups of the formulas -C (O) -, -C (O) 0 -, -C (0) NR 5 -, - NR 5 -, -N ⁇ R 5 -, -N + R 5 R 5 -, -0- or -S- interrupted and
- x an integer from 1-20
- y the values 0 or 1, z depending on the value of R 4 the values 1, 2 or 3, h the values 0 or 1, m an integer from 1-20
- a, b and c each represents the values 0, 1, 2, 3 or 4 and the sum a + b + c less than or equal to 4 and e, f and g each represent an integer from 0-200, with the proviso that the sum e + f + g> 1.
- organosilicon compounds can optionally contain units of the general formulas (V) and (VI), O (4. I - k _ 1) / 2 R i X k Si-A i -SiX lc R : l 0 ⁇ 4 . i . k . 1) / 2 (V),
- a a has a trivalent hydrocarbon radical 1 to 200 carbon atoms means the radicals of the formulas " - C (O) -, -C (0) 0-, -C (0) NR 5 , -NR 5 -, -N + HR 5 -, -N + R 5 R 5 -, -0-, -S-, - N- or -N + R 5 - interrupted and / or substituted with F, Cl or Br,
- a 1 represents a divalent radical R 2 , i and kj each mean the values 0, 1, 2 or 3, with the proviso i + k ⁇ 3 and
- R and X have the meanings given above.
- hydrocarbon radicals R, R 1 , R 2 , R 3 , R 4 , R s , A 1 and A 2 listed above can be saturated, unsaturated, linear, cyclic, aromatic or non-aromatic.
- hydrocarbon radicals R are alkyl radicals, such as methyl, ethyl, n-propyl, iso-propyl, 1-n-butyl, 2-n-butyl
- Hexyl radicals such as the n-hexyl radical
- Heptyl residues such as the n-heptyl residue
- Octyl residues such as the n-
- Octyl radical and iso-octyl radicals such as the 2, 2, 4-trimethylpentyl radical
- Nonyl radicals such as the n-nonyl radical Decyl radicals, such as the n-decyl radical
- Dodecyl radicals such as the n-dodecyl radical
- Octadecyl radicals such as the n-octadecyl radical
- Cycloalkyl radicals such as the cyclopentyl, cyclohexyl, cycloheptyl radical and methylcyclohexyl radicals
- Aryl radicals such as the phenyl, ISjaphthyl, anthryl and phenanthryl radical
- Alkaryl residues such as o-, m-, p-tolyl residues
- aralkyl radicals such as the benzyl radical, the ⁇ -
- the hydrogen atom or the methyl, ethyl, octyl and phenyl radical are preferred, and the hydrogen atom or the methyl and ethyl radical are particularly preferred.
- halogenated radicals R are haloalkyl radicals, such as the 3,3,3-rifluoro-n-propyl radical, the 2 " , 2, 2, 2 ', 2', 2'-hexafluoro-isopropyl radical, the heptafluoroisopropyl radical and halogenaryl radicals, such as the o-, m- and p-chlorophenyl.
- radical R 1 examples are the examples given for radical R equal to alkyl radicals as well as the methoxyethyl and ethoxyethyl radical, the radical R 1 preferably being alkyl radicals having 1 to 50 carbon atoms which can be interrupted by oxygen atoms, particularly preferably methyl - and deals with the ethyl radical.
- Alkali and alkaline earth metal ions, ammonium and phosphonium ions and mono- or trivalent metal ions are preferred.
- Alkali ions particularly preferably Na + and K + .
- radicals X are the methoxy or ethoxy radical and the general formula (II), such as
- radicals R 2 are linear or branched, substituted or unsubstituted hydrocarbon radicals with preferably 2 to 10 carbon atoms, where saturated or unsaturated alkylene radicals are preferred and the ethylene or propylene radical are particularly preferred.
- radicals R 3 are the examples and radicals of the formula —C (0) R 1 or —Si (R 1 ) 3 , given for R equal to the alkyl radical or aryl radical, the methyl, ethyl, propyl and butyl and trialkylsilyl - and -C (0) -alkyl radical are preferred and the methyl, butyl -, —C (0) -CH 3 and the trimethylsilyl radical are particularly preferred.
- R 4 is preferably a radical of the formula - (CH 2 ) 3 -
- R 4 are - (CH 2 ) 3 - and - (CH 2 ) 3 -NH- (CH 2 ) 2 -.
- R s are the alkyl and aryl radicals listed above for R and radicals of the formulas -C (0) -CH 3
- the hydrogen atom and the examples given for R are preferred, and the hydrogen atom and alkyl radicals are particularly preferred.
- Examples of A 1 are linear or branched, divalent alkyl radicals having preferably 2 to 20 carbon atoms, or radicals of the formulas - (CH 2 ) 3 -NH- (CH 2 ) 3 -, - (CH 2 ) 3 -NR 5 - (CH 2 ) 3 - - (CH 2 ) 3 - (CH 2 -CH 2 0) f - (CH 2 ) 3 - -0- (CH 2 -CH 2 0) f -
- Example of A 2 is N [(CH 2 ) 3 -]
- Organosilicon compounds (A) can also be formed from raw products during the process.
- organosilicon compounds (A) are linear trimethylsilyl or hydroxydiethylsilyl terminals
- Oils with a viscosity of 50 mPas Oils with a viscosity of 50 mPas
- resinous organosilicon compounds (A) are methyl ethoxy resins, e.g. of the formula
- organosilicon compound (A) itself acts as an emulsifier, then organosilicon compound (A) and emulsifier can
- the component (B) of the emulsions is preferably commercially available and well-studied emulsifiers, such as, for example, sorbitan esters of fatty acids having 10 to 22 carbon atoms; Polyoxyethylene sorbitan esters of fatty acids with 10 to 22 carbon atoms and up to 35 percent ethylene oxide; Polyoxyethylene sorbitol esters of fatty acids with 10 to 22 carbon atoms, • Polyoxyethylene derivatives of phenols with 6 to 20 carbon atoms on the aromatic and up to 95 percent
- ethylene oxide Fatty amino and amido betaines having 10 to 22 carbon atoms; Polyoxyethylene condensates of fatty acids or fatty alcohols with 8 to 22 carbon atoms with up to 95 Percent ethylene oxide content; ionic emulsifiers, such as alkylarylsulfonates having 6 to 20 carbon atoms in the alkyl group; Fatty acid soaps with 8 to 22 carbon atoms; Fatty sulfates having 8 to 22 carbon atoms; Alkylene sulfonates having 10 to 22 carbon atoms; Alkali metal salts of dialkyl sulfosuccinates; Fatty amine oxides having 10 to 22 carbon atoms; Fatty imidazolines having 6 to 20 carbon atoms; Fatty amido sulfobetaines having 10 to 22 carbon atoms; quaternary emulsifiers, such as fatty ammonium compounds having 10 to 22 carbon atoms; Fat morpholine oxides with 10 to 22 carbon atoms
- Organosilicon compounds (A) which have units of the general formula I in which X is a radical of the general formula II and c is at least 1.
- the counterions in the case of anionic emulsifiers can be alkali metals, ammonia or substituted amines such as trimethanolamine or triethanolamine. Usually ammonium, sodium and potassium ions are preferred.
- the counter ion is a halide, sulfate or methyl sulfate. Chlorides are the mostly industrially available compounds.
- the above-mentioned fat structures usually represent the lipophilic half of the emulsifiers.
- a common fat group is an alkyl group of natural or synthetic origin. Known unsaturated groups are the oleyl, linoleyl, Decenyl, hexadecenyl and dodecenyl residues. Al alkyl groups can be cyclic, linear or branched. Other possible emulsifiers are sorbitol mon ⁇ laurate ethylene oxide condensates; Sorbitol monomyristate ethylene oxide condensates; Sorbitolmonostearat-
- Ethylene oxide condensates Dodecylphenol ethylene oxide condensates; Myristylphenol-ethylene oxide condensates; Octylpt ⁇ enyl ethylene oxide condensates; Stearylphenol ethylene oxide condensates; Lauryl alcohol ethylene oxide condensates; Stearyl alcohol ethylene oxide condensates; decyl amino; Cocoamidsulfobetain; Olylamidobetain; Cocoi idazolin; Cocosulfoimidazolin; Cetylimidazolin; l-hydroxyethyl-2-heptadecen; yl-imidazoline; n-cocomorpholine oxide; Decyldimeth; ylaminoxid; '' Cocoamidodimethylamine oxide; Sorbitan tristearate with condensed ethylene oxide groups; Sorbitan trioleate with condensed
- Ethylene oxide groups Sodium or potassium dodecyl sulfate; Sodium or potassium stearyl sulfate; Sodium or potassium dodecylbenzenesulfonate; Sodium or potassium stearyl sulfonate; Triethanolan ⁇ insalz des Dodecylsulfates; trimethyldodecylammonium;
- Trimethylstearylammonium methosulfate Sodium laurate; Sodium or potassium myristate.
- inorganic solids can also be used as emulsifiers (B).
- B emulsifiers
- the nonionic emulsifiers are preferred.
- the component (B) can from an o. g. Emulsifiers or from a mixture of two or more o. g. Emulsifiers exist, it can be in pure form or as solutions of one or more Emulsifiers can be used in water or organic solvents.
- Emulsifiers (B) are used in amounts of preferably 0.1 to 60% by weight, particularly preferably 1 to 30% by weight, in each case based on the total weight of organosilicon compounds. (A) used.
- additives such as silanes, acids, alkalis, biocides, thickeners, silicas and water-soluble polysiloxians, can be added in addition to water and emulsifiers.
- silanes examples include vinyltris (methoxyethoxy) silane, tetraethoxysilane, anhydrolyzed tetraethoxysilane, methyltriethoxysilane, anhydrolyzed methyltriethoxysilane, aminoethylaminopropyltrimethoxysilane, aminoethylaminopropyl (methyl) dimethoxysilane.
- Lines A, B, C, D feed at least one emulsifier (B) or a solution of an emulsifier (B) and optionally water (C), optionally one or more organosilicon compounds (A) and additives (Z) into line 1 dosed continuously.
- a static mixing element can optionally be installed in the feed line 1 in order to improve the mixing of the components upstream of the first high-shear mixer 2. After the first mixer 2, a rigid phase is generated. After mixer 2 are one
- the predetermined temperature and the predetermined pressure in line 5 are controlled by the pressure control valve 22 and Speed of the high shear mixer 2 set.
- the temperature is regulated by the temperature of the raw materials, which are tempered according to the specifications, and by the speed of the mixer.
- One or more emulsifiers (B), one or more, can again be fed continuously into the feed line 5
- Organosilicon compounds (A), water (C) and additives (Z) are added.
- the mixture or solid phase can also be transferred into the second high-shear mixer 6 without metering.
- the temperature after mixer 6 is measured by the temperature sensor 7 and with the temperature de x
- Raw materials and the speed of the mixer 6 regulated.
- the pressure downstream of the mixer 6 is measured by the pressure sensor 8 and regulated with the pressure holding valve 22 and the speed of the mixer 6.
- one or more emulsifiers (B), one or more organosilicon compounds (A), water (C) and additives (Z) can be metered in again.
- the product can then be passed in line 24 to the mixer 13 via an optionally available valve 9 and an optionally available line 10 or further fed to the high-shear mixer 18 in line 24 via an optionally available valve 17.
- 13 raw materials can be dosed in front of the mixer.
- the temperatures and pressures downstream of mixer 13 and mixer 18 are detected by the temperature controllers 14 and 19 and the pressure sensors 15 and 20, as described above, and are regulated as described previously. If the route of the product via line 10 is not used, premixes or premulsions can be produced in the mixer in the manner described and fed to the product in front of mixer 18.
- the temperature and pressure control is analog. After mixer 18, further emulsifiers (B),
- Organosilicon compounds (A), water (C), additives (Z) are added. Furthermore, there is the possibility of further adding the emulsion with water after the pressure-maintaining valve 22 dilute before filling the finished product into a tank or sales container.
- Example 1 Preparation of a clear emulsion of an amino functional polysiloxane.
- Mixer 2 (4000 rpm) is mixed with 16.25% amino-functional silicone oil (Wacker® Finish WR 1300) at a temperature of 40 ° C (the temperature is regulated to + 2 K) ⁇ 1.60% isotridecyl alcohol ethoxylate with an average of 8 EO (Arlypon ® IT 8), 4.14% isotridecyl alcohol ethoxylate with an average of 5 EO (Lutensol® TO 5), 0.2% acetic acid (80%) and 3.93% deionized water (temperature 12 ° C, the temperature is increased to + 2 K regulated).
- the pressure control valve 22 is set to 4.5 bar.
- the product produced shows a significantly larger particle size of 42 nm and a turbidity of 23 ppm.
- Example 2 Preparation of a polyvinyl alcohol stabilized silicone resin emulsion
- Mixer 2 (4000 RPM) is 35.3% polyvinyl alcohol solution (10%) (25 ° C, the temperature is kept constant at + 2 K) and 48.4% of a mixture of silicone resin (80 mol% T units 20 Mol% D units, 20 ° C) with one. OH terminated polydimethylsiloxane with a viscosity of 30 mPas and 4.7% deionized water (12 ° C). This mixture is fed to mixer 6 and sheared again in mixer 6 (3000 rpm). After mixer 6, 11.36% deionized water (12 ° C) and 0.24% preservative (Roci a® 523) was added and the mixture was fed to mixer 18 (3000 rpm). The pressure control valve 22 is set to 2 bar.
- the temperature after mixer 2 increases to about 45 ° C. and accordingly. Temperature after mixer 6 and 22 to 46 ° C.
- the product obtained shows a clear deposition of silicone resin after 2 weeks of storage at room temperature.
- Mixer 2 (4000 rpm) is mixed with 34.88% of an OH-functional polydimethylsiloxane (15 ° C.) with a viscosity of about 30 mPas and 3.7% of an isotridecyl alcohol ethoxylate with 10 EO units (80% solution in water) and 4. 5% deionized water and 3% dodecylbenzenesulfonic acid.
- This mixture is fed to mixer 6 (3000 rpm) and worked through there again.
- the mixture is fed to mixer 18 and 40.43% demineralized water and 0.08% preservative (Kathon® LXE) are metered in before mixer 18 (3000 rpm).
- the pressure control valve 22 is set to 3 bar.
- This mixture is then stored in a container for an average residence time of 7.5 hours. An acid-catalyzed condensation of the polydimethylsiloxane takes place there. After 7.5 hours, 2.1% triethanohamine (80%) and 11.27% deionized water are added. This neutralizes the acid and ends the reaction.
- polydimethylsiloxane is operated at 25 ° C, an emulsion results which has a comparable particle size (154 nm) but only an oil viscosity of 60,000 mPas which is too low.
Abstract
Description
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Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/599,869 US20070203263A1 (en) | 2004-04-15 | 2005-04-14 | Process For The Continuous Preparation Of Silicone Emulsions |
CN2005800111516A CN1942509B (zh) | 2004-04-15 | 2005-04-14 | 连续制备聚硅氧烷乳液的方法 |
DE502005000987T DE502005000987D1 (de) | 2004-04-15 | 2005-04-14 | Verfahren zur kontinuierlichen herstellung von siilicon emulsionen |
JP2007507761A JP5154219B2 (ja) | 2004-04-15 | 2005-04-14 | シリコーンエマルジョンを連続的に製造する方法 |
EP05733302A EP1735370B1 (de) | 2004-04-15 | 2005-04-14 | Verfahren zur kontinuierlichen herstellung von siilicon emulsionen |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102004018283A DE102004018283A1 (de) | 2004-04-15 | 2004-04-15 | Verfahren zur kontinuierlichen Herstellung von Silicon Emulsionen |
DE102004018283.3 | 2004-04-15 |
Publications (1)
Publication Number | Publication Date |
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WO2005100453A1 true WO2005100453A1 (de) | 2005-10-27 |
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Application Number | Title | Priority Date | Filing Date |
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PCT/EP2005/003960 WO2005100453A1 (de) | 2004-04-15 | 2005-04-14 | Verfahren zur kontinuierlichen herstellung von siilicon emulsionen |
Country Status (7)
Country | Link |
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US (1) | US20070203263A1 (de) |
EP (1) | EP1735370B1 (de) |
JP (1) | JP5154219B2 (de) |
KR (1) | KR100782441B1 (de) |
CN (1) | CN1942509B (de) |
DE (2) | DE102004018283A1 (de) |
WO (1) | WO2005100453A1 (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8304023B2 (en) | 2006-11-08 | 2012-11-06 | Wacker Chemie Ag | Treatment of fiberfill fibers with aqueous dispersions of organopolysiloxanes |
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JP2013539485A (ja) * | 2010-08-03 | 2013-10-24 | ダウ コーニング コーポレーション | シリコーンゴムエマルション |
CN102961987A (zh) * | 2012-12-18 | 2013-03-13 | 江南大学 | 具有预混合的连续化高粘硅油乳化工艺及其设备 |
CN103665395B (zh) * | 2013-12-04 | 2016-01-20 | 济南开发区星火科学技术研究院 | 一种硅油的制备方法 |
CA2956081C (en) | 2014-08-27 | 2021-03-16 | The Procter & Gamble Company | Detergent composition comprising a cationic polymer |
JP6400837B2 (ja) | 2014-08-27 | 2018-10-03 | ザ プロクター アンド ギャンブル カンパニー | 布地の処理方法 |
US9951297B2 (en) | 2014-08-27 | 2018-04-24 | The Procter & Gamble Company | Detergent composition compromising a cationic polymer containing a vinyl formamide nonionic structural unit |
WO2016032992A1 (en) | 2014-08-27 | 2016-03-03 | The Procter & Gamble Company | Detergent composition comprising a cationic polymer |
JP6430632B2 (ja) | 2014-09-25 | 2018-11-28 | ザ プロクター アンド ギャンブル カンパニー | ポリエーテルアミンを含有する布地ケア組成物 |
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- 2005-04-14 JP JP2007507761A patent/JP5154219B2/ja active Active
- 2005-04-14 DE DE502005000987T patent/DE502005000987D1/de active Active
- 2005-04-14 US US10/599,869 patent/US20070203263A1/en not_active Abandoned
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Also Published As
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DE102004018283A1 (de) | 2005-11-03 |
CN1942509A (zh) | 2007-04-04 |
JP5154219B2 (ja) | 2013-02-27 |
CN1942509B (zh) | 2010-07-14 |
JP2007532736A (ja) | 2007-11-15 |
US20070203263A1 (en) | 2007-08-30 |
EP1735370A1 (de) | 2006-12-27 |
KR100782441B1 (ko) | 2007-12-05 |
KR20060129464A (ko) | 2006-12-15 |
EP1735370B1 (de) | 2007-07-04 |
DE502005000987D1 (de) | 2007-08-16 |
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