Classifications

• • 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
  • C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
  • C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
  • C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
  • C08G69/14—Lactams
  • C08G69/16—Preparatory processes
  • C08G69/18—Anionic polymerisation
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
  • B29C64/00—Additive manufacturing, i.e. manufacturing of three-dimensional [3D] objects by additive deposition, additive agglomeration or additive layering, e.g. by 3D printing, stereolithography or selective laser sintering
  • B29C64/10—Processes of additive manufacturing
  • B29C64/141—Processes of additive manufacturing using only solid materials
  • B29C64/153—Processes of additive manufacturing using only solid materials using layers of powder being selectively joined, e.g. by selective laser sintering or melting
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
  • B29C67/00—Shaping techniques not covered by groups B29C39/00 - B29C65/00, B29C70/00 or B29C73/00
  • B29C67/02—Moulding by agglomerating
  • B29C67/04—Sintering
• • 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
  • C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
  • C08G69/44—Polyester-amides
• • 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
  • C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
  • C08G69/46—Post-polymerisation treatment
• • 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
  • C08J3/12—Powdering or granulating
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
  • C08L77/02—Polyamides derived from omega-amino carboxylic acids or from lactams thereof
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
  • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
  • B29K2077/00—Use of PA, i.e. polyamides, e.g. polyesteramides or derivatives thereof, as moulding material

Definitions

• Porous powder particles of polyamide, copolyamide or copolyesteramide are spherical or quasi-spherical particles, with a mean diameter of less than 100 ⁇ m, preferably less than 50 ⁇ m.
• These particles having a controlled specific surface area (SSA) are a major asset in applications such as: composite materials, transfer papers, coating of substrates, especially metal (coil-coating), ink and paint compositions solid or liquid, the agglomeration of polyamide powders by compression with or without metal particles or by sintering or melting caused by radiation such as for example a laser beam (laser sintering), infrared radiation or UV radiation ( UV curing), cosmetic and / or pharmaceutical formulations.
• laser beam laser sintering
• UV radiation UV curing
• Patent EP0192515 describes the anionic polymerization of a lactam in a reactor stirred in a solvent in the presence of a catalyst, an activator, an N, N'-alkylenebisamide and optionally an organic or inorganic filler. .
• the size of the grains can be compensated by varying different process parameters such as the reaction temperature, the catalyst content, the activator injection rate, the stirring speed and the filler content.
• the particles of polyamide powders on the market show that for a mean diameter which is increasing, the SSA decreases as shown in Table A above.
• particles of polyamide, copolyamide or copolyesteramide powder which, for the same average diameter, are available in the widest range of apparent surface area (SSA) possible with SSA, preferably the highest possible or for the same SSA, are available in a range of the largest average diameter with a mean diameter, preferably as low as possible.
• SSA apparent surface area
• the Applicant has now found a solution to this technical problem and shows below that to obtain particles of polyamide, copolyamide or copolyesteramide narrow particle size distribution, average diameter less than 100 microns, preferably less than 50 microns, preferably less than 30 ⁇ m, even more advantageously less than 20 ⁇ m and SSA less than 50 m2 / g, advantageously less than 40 m2 / g, still more advantageously less than 30 m2 / g, the anionic polymerization in solution in a solvent of the monomer or monomers, generators of said polymer, is carried out in the presence of a catalyst, an activator, at least one amide, one of which is always a N, N'-alkylene bis amide and a mineral or organic filler, the amount of N
• the N'-alkylenebisamide added in the medium is determined as a function of the Apparent Surface Specificity (SSA) and / or the average particle diameter desired.
• SSA Apparent Surface Specificity
• Seeding is when the thickness of the polymer layer of the final seeded particle is greater than the radius of the feed whose density is at most 4.5 cm3 / g. And conversely, we speak of coating, when the thickness of the polymer layer of the final coated particle is less than the radius of the charge whose density is at most 4.5 cm3 / g.
• Fig.1 is a photograph of the powder according to the invention obtained in Ex.1
• Fig.2 is a photograph of the powder according to the invention obtained in Ex.2.
• the subject of the invention is a process for producing a polymer powder chosen from a polyamide, a copolyamide or an anionic polymerization copolyesteramide in solution in a solvent, characterized in that the said polymerization of the monomer (s) generating said polymer is carried out. in the presence:
• At least one amide chosen from N, N'-alkylenebisamide, and
• SSA specific surface area
• the process for manufacturing a polymer powder chosen from a polyamide, a copolyamide or an anionic polymerization copolyesteramide in solution in a solvent is characterized in that said polymerization of the monomer (s) generating said polymer is performed in the presence:
• At least one amide chosen from N, N'-alkylenebisamide, and
• SSA apparent surface area
• the method is characterized in that as the amount of amide increases, the SSA increases.
• the method is characterized in that as the amount of amide increases, the average diameter decreases.
• the process is characterized in that the monomer (s) generating the polymer is or are chosen from lactams such as lauryllactam, caprolactam, oenantholactam, capryllactam or their mixtures, preferably , lauryllactam alone, caprolactam alone or their mixture.
• lactams such as lauryllactam, caprolactam, oenantholactam, capryllactam or their mixtures, preferably , lauryllactam alone, caprolactam alone or their mixture.
• the process is characterized in that the monomers generating the polymer are a mixture comprising in mole%, the total being 100%: 1-98% of a lactam selected from lauryllactam, caprolactam, oenantholactam and capryllactam;
• lactam different from the first one selected from lauryllactam, caprolactam, oenantholactam and capryllactam;
• a lactone selected from caprolactone, valerolactone and butyrolactone; advantageously 30-46% caprolactam, 30-46% lauryllactam and 8-40% caprolactone.
• the process is characterized in that the catalyst is selected from sodium hydride, potassium hydride, sodium, methylate and sodium ethoxide.
• the process is characterized in that the activator is chosen from lactams-N-carboxyanilides, (mono) isocyanates, polyisocyanates, carbodiimides, cyanamides, acyllactams and acylcarbamates, triazines, ureas, N-substituted imides, esters and phosphorus trichloride.
• the activator is chosen from lactams-N-carboxyanilides, (mono) isocyanates, polyisocyanates, carbodiimides, cyanamides, acyllactams and acylcarbamates, triazines, ureas, N-substituted imides, esters and phosphorus trichloride.
• the activator is selected from lactams-N-carboxyanilides, (mono) isocyanates, polyisocyanates, carbodiimides, cyanamides, acyllactams and acylcarbamates, triazines, ureas, N-substituted imides, esters and trichloride. phosphorus.
• the process is characterized in that the N, N'-alkylenebisamide is chosen from N, N'-ethylene bis-stearamide (EBS) and N, N'-ethylene bis-oleamide (EBO ).
• EBS N, N'-ethylene bis-stearamide
• EBO N, N'-ethylene bis-oleamide
• the process is characterized in that the inorganic filler is chosen from silicas, aluminosilicates, aluminum oxides or alumina, titanium dioxides and BN.
• the process is characterized in that the organic filler is chosen from homo or copolyamide polyamide powders, preferably PA12, PA1 1, PA6, PA6-12, PA 6.12, PA 6.6, PA8, PA4. , polystyrenes, polyurethanes, poly (methyl) methacrylates (PMMA), polyacrylates, polyesters, silicones, polyethylenes, polytetrafluoroethylene.
• the process is characterized in that the particle distribution is narrower than that of the particles obtained by the process defined above. According to one embodiment, the process is characterized in that the particles of powders obtained have a mean diameter ⁇ 30 microns, advantageously ⁇ 20 microns.
• the method is characterized in that the SSA ⁇ 40 m 2 / g, advantageously ⁇ 30 m 2 / g.
• the invention also relates to polymer powder particles chosen from a polyamide, a copolyamide or a copolyesteramide obtained according to the process defined above.
• the particles are characterized in that the organic filler is an Orgasol®.
• the invention also relates to a composition of the preceding particles, characterized in that it further comprises at least one compound selected from carbon nanotubes, metal particles, pigments, dyes, antioxidants, anti-UV , plasticizers and carbon black.
• the invention furthermore relates to the use of the powder particles obtained according to the process described above, the particles previously described or the composition defined above for producing composite materials, transfer papers, substrate coatings, especially coatings.
• metal coatings coatings
• solid or liquid compositions of inks or paints solid or liquid compositions of inks or paints
• cosmetic compositions and / or pharmaceutical compositions according to one embodiment, for producing articles by agglomeration of said powder alone or in composition by compression or sintering or melting caused by radiation such as a laser beam (laser sintering), infrared radiation or UV radiation (UV curing).
• a substantially constant diameter means that for the same process, the average diameter of the particles obtained from one batch to another may vary within a diameter range of plus or minus 20% relative to the average of the average diameters of the different batches. For example, for batches whose average average diameter is 10 .mu.m, the range of variation is between 8 and 12 .mu.m.
• a substantially constant SSA means that for the same process, the average SSA of the particles obtained from one batch to the next can vary within a range of SSA of plus or minus 25% compared to the mean of the average SSA of the different batches. For example, for batches whose SSA average is 4 m 2 / g, the range of variation is between 3 and 5 m 2 / g.
• the polymerizable monomer (s) used in the invention is or are chosen from lactams such as, for example, lauryllactam, caprolactam, oenantholactam, capryllactam or their mixtures.
• lactams such as, for example, lauryllactam, caprolactam, oenantholactam, capryllactam or their mixtures.
• lauryllactam alone, caprolactam alone or their mixture is used.
• lactam selected from lauryllactam, caprolactam, oenantholactam and capryllactam;
• lactam different from the first one selected from lauryllactam, caprolactam, oenantholactam and capryllactam;
• caprolactam, lauryllactam and caprolactone are advantageously used in the following proportions (mol%): 30-46%, 30-46% and 8-40% (the total being 100% ).
• the method is applicable to lactams and mixtures thereof rather than mixtures of several lactams and a lactone.
• the solvent used dissolves the monomer (s) but not the polymer particles that form during the polymerization.
• the solvent are given in patent EP192515.
• the solvent is a paraffinic hydrocarbon fraction whose boiling range at atmospheric pressure is between 120 and 170 ° C, preferably between 140 and 170 ° C.
• the solvent may be supersaturated to monomer (s) at the initiation temperature, i.e. at the temperature at which the polymerization begins.
• Various means make it possible to supersaturate the solvent with monomer (s).
• One of these means can consist in saturating the solvent with monomer (s) at a temperature higher than that initiation, then lowering the temperature to the initiation temperature.
• Another means may consist in substantially saturating the solvent with monomer (s) at the initiation temperature, then adding, always at this temperature, a primary amide preferably containing from 12 to 22 carbon atoms, for example oleamide, N-stearamide, erucamide, isostearamide or a N 1 N'-alkylenebisamide examples of which are given below.
• the reaction medium contains the monomer (s) dissolved in the solvent at a concentration remote from the supersaturation at the initiation temperature.
• a catalyst selected from the usual catalysts of the anionic polymerization of lactams is used. This is a base strong enough to lead to a lactamate after reaction with the lactam or the mixture of lactams.
• a combination of several catalysts is possible.
• the amount of catalyst (s) introduced can generally vary between 0.5 and 3 moles per 100 moles of monomer (s).
• the activator is also added whose role is to provoke and / or accelerate the polymerization.
• the activator is chosen from lactams-N-carboxyanilides, (mono) isocyanates, polyisocyanates, carbodiimides, cyanamides, acyllactams and acylcarbamates, triazines, ureas, N-substituted imides, esters and trichloride. of phosphorus. It may also be a mixture of several activators.
• the activator may also optionally be formed in situ, for example, by reacting an alkyl isocyanate with the lactam to give an acyl lactam.
• the catalyst / activator molar ratio is between 0.2 and 2, preferably between 0.8 and 1.2.
• At least one amide, one of which is always an N, N'-alkylenebisamide, is also added as indicated in EP192515.
• the amount of N, N'-alkylenebisamide (s) introduced is generally of the order of 0.001 to 4 moles, preferably 0.075 to 2 moles per 100 moles of monomer (s).
• N, N'-alkylenebis amides particularly recommended mention may be made of N, N'-alkylene bis amides of fatty acids and better still:
• EBS and / or EBO are used.
• a primary amide preferably containing from 12 to 22 carbon atoms. It may be chosen from: oleamide, N-stearamide, isosteramide and erucamide.
• the inorganic filler its density is at most 4.5 cm3 / g and it is chosen from silicas, ainosinicates, aluminum oxides or alumina, titanium dioxides, BN (for example Very BN ⁇ Saint Gobain). IE may also be a mixture of these mineral fillers.
• a mixture of mineral fillers mentioned above there may be found as examples a mixture of different silicas, a mixture of a silica and an alumina, or a mixture of a silica and a carbon dioxide. titanium.
• the organic filler its density is at most 4.5 cm3 / g and it is a homo or copolyamide polyamide powder, preferably of PA12, PA1 1, PA6, PA6 / 12, PA 6.12, PA 6.6, PA8, PA4 (for example Arkema's Orgasol® powders, Degussa's Vestosint® powders, etc.), polystyrenes, polyurethanes, poly (methyl) methacrylates (PMMA), polyesters, silicones , polyethylenes, polytetrafluoroethylene.
• the amount of inorganic or organic fillers and the diameter of said fillers make it possible to orient in the desired direction (small particles or large particles) the size of the final particles obtained at the end of the polymerization.
• fillers pigments, dyes, carbon black, carbon nanotubes, etc.
• additives antioxidants, anti-UV, plasticizers, etc.
• the anionic polymerization is conducted continuously or preferably batchwise.
• the solvent is introduced, then simultaneously or successively the monomer (s), optionally an N, N'-alkylenebisamide, the filler, the catalyst and the activator. It is recommended to first introduce the solvent and the monomer (s) and then remove water, for example using azeotropic distillation, then add the catalyst once the medium comprising the least possible molecule of water.
• the charge can be introduced for example after the introduction of the monomer (s). It may be advantageous to prevent the caking or the loss of control of the polymerization from introducing the activator not all at once at a time t, but at one time over a longer or shorter period of time at a time. constant speed or with a speed gradient, either in stages with different speeds for each step.
• the reaction is carried out at atmospheric pressure or under a slightly higher pressure (partial pressure of the hot solvent) and at a temperature of between 20 ° C. and the boiling point of the solvent.
• the initiation and polymerization temperature of the lactams is in general between 70 and 150 ° C, preferably between 80 and 130 ° C.
• the weight ratio [organic or inorganic filler / monomer (s) introduced into the reaction medium] expressed in% is between 0.001% and 65%, preferably between 0.005% and 45% and even more preferably between 0% and 0%. , 01 and 30%, and advantageously between 0.05 and 20%.
• the powders according to the invention can be used in the context of the method of manufacturing objects by melting caused by a laser beam (laser sintering), IR radiation or UV radiation.
• laser sintering laser sintering
• IR radiation IR radiation
• UV radiation UV radiation.
• the laser sintering technique is described in patent application EP1571173 of the applicant.
• the analysis of the powders obtained in the Examples and Comparative below is carried out using a Coulter LS230 granulometer. It makes it possible to obtain the particle size distribution of the powders from which one can determine:> the average diameter. > The width of the distribution or the standard deviation of the distribution.
• the particle size distribution of the powders according to the invention is determined according to the usual techniques using a Coulter LS230 granulometer from Beckman-Coulter. From the particle size distribution, it is possible to determine the volume average diameter with the logarithmic calculation method version 2.1 1 a. of the software, as well as the standard deviation that measures the narrowing of the distribution or the width of the distribution around the mean diameter. It is one of the advantages of the method described here that to obtain a narrow distribution (low standard deviation) with respect to the average diameter. This standard deviation is calculated using the logarithmic statistical calculation method, version 2.1 1a. of the software.
• the apparent specific surface area of the particles was measured by BET method (ten points) with SA3100 from BECKMANN-COULTER.
• the BET method (BRUNAUER-EMMET-TELLER) is a method well known to those skilled in the art. It is described in particular in "The Journal of the 30 American Chemical Society", vol.60, page 309, February 1938 and corresponds to the international standard ISO 5794/1 (Appendix D).
• the specific surface area measured according to the BET method corresponds to the total surface area, that is to say it includes the surface formed by the pores.
• the BET technique involves absorbing a monomolecular layer of gas molecules on the surface. The gas used is nitrogen.
• 2210 ml of solvent are introduced into the reactor maintained under nitrogen, followed successively by 719 g of dry lauryllactam, 21.5 g of EBS, 0.45 g of N-stearamide and 13.8 g of finely divided AEROSIL® R972 silica. After stirring at 350 rpm, the mixture is gradually heated to 110 ° C., and then 265 ml of solvent are distilled off under vacuum so as to azeotrope traces of water which may be present.
• the anionic catalyst 1.44 g of sodium hydride at 60% purity in oil, is rapidly introduced under nitrogen, and stirring is increased at 650 rpm, under nitrogen at 110 ° C for 30 minutes.
• the temperature is brought to 95 ° C. and, thanks to a small dosing pump, a continuous injection into the reaction medium of the activator is carried out.
• the temperature is maintained at 95 ° C. for the first 300 minutes, then is raised to 120 ° C. in 30 minutes and maintained at 120 ° C. for a further 2 hours after the end of introduction of the isocyanate.
• the particle size is between 1 and 20 ⁇ m, the average particle diameter is 6 ⁇ m without agglomerate and the SSA is 20.7 m 2 / g.
• Example 1 is repeated, but 14.5 g of EBS is used. The polymerization completed, the reactor is almost clean. The particle size is between 1 and 20 microns, the average particle diameter is 6.3 microns without agglomerate and the SSA is 7.1 m 2 / g.
• Example 3 Comparing Example 1 and Example 2, it is found that the decrease in the amount of EBS causes a significant drop in the SSA for a comparable particle size.
• 2800 ml of solvent are introduced into the reactor maintained under nitrogen, followed successively by 899 g of dry lauryllactam, 27.7 g of EBS, 0.45 g of N-stearamide and 3.6 g of finely divided AEROSIL® R972 silica. After stirring at 350 rpm, the mixture is gradually heated to 110 ° C. and then 290 ml of solvent are distilled off under vacuum in order to azeotrope traces of water which may be present.
• the anionic catalyst 1.44 g of sodium hydride at 60% purity in oil, is rapidly introduced under nitrogen, and the stirring is increased to 720 r / min. nitrogen at 110 ° C for 30 minutes. Then, the temperature is brought to 99.7 ° C. and, thanks to a small metering pump, a continuous injection is made into the reaction medium of the chosen activator, namely stearyl isocyanate (55.7 g filled to 237 ° C.). , 7 g with solvent), according to the following program:
• the polymerization is then complete, the reactor is almost clean.
• the particle size is between 2 and 25 ⁇ m, the average particle diameter is 10.0 ⁇ m and the SSA 12.2 m 2 / g without agglomerate.
• the same conditions are used as in Example 3, but no N-stearamide is added.
• the polyamide powder 12 obtained has the following characteristics:
• the anionic catalyst 9 g of sodium hydride at 60% purity in oil
• the stirring is increased to 720 rpm under nitrogen at room temperature. 1 10 ° C for 30 minutes.
• the temperature is brought to 81 ° C. and, thanks to a small metering pump, a continuous injection is made into the reaction medium of the chosen activator, namely stearyl isocyanate (32.9 g filled to 323.9 ° C.). g with solvent), according to the following program:
• the temperature is maintained at 81 ° C. for the first 300 minutes, then is raised to 110 ° C. in 60 minutes and maintained at 110 ° C. for a further 3 hours after the end of introduction of the isocyanate.
• the polymerization is then complete, the reactor is almost clean.
• the particle size is between 2 and 25 microns, the average particle diameter is 1.17 microns and the SSA is 28.8 m 2 / g without agglomerate.
• Example 5 is repeated, but only 7.2 g of EBS is used. The polymerization completed, the reactor is almost clean. The particle size is between 2 and 25 ⁇ m, the average particle diameter is 13.7 ⁇ m and the SSA is 15.9 m 2 / g without agglomerate.
• the anionic catalyst 7.2 g of sodium hydride at 60% purity in oil, are rapidly introduced under nitrogen and the stirring is increased to 720 r / min under nitrogen at 110 ° C for 30 minutes.
• the temperature is brought to 96 ° C. and, thanks to a small dosing pump, a continuous injection into the reaction medium of the chosen activator, namely stearyl isocyanate (32.9 g filled to 314 g with solvent), according to the following schedule:
• the temperature is maintained at 96 ° C. for the first 360 minutes, then is raised to 110 ° C. in 60 minutes and maintained at 110 ° C. for a further 2 hours after the end of introduction of the isocyanate.
• Example 7 is repeated, but 24.7 g of EBS is used. The polymerization completed, the reactor is almost clean. The particle size is between 1 and 20 microns, the average particle diameter is 1 1, 4 microns without agglomerates and the SSA is 13.2 m 2 / g.
• Example 9
• Example 7 is repeated, but 30.9 g of EBS is used. The polymerization completed, the reactor is almost clean. The particle size is between 1 and 20 microns, the average particle diameter is 11.4 microns without agglomerate and the SSA is 15 m 2 / g.

Landscapes

• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Optics & Photonics (AREA)
• Physics & Mathematics (AREA)
• Materials Engineering (AREA)
• Mechanical Engineering (AREA)
• Manufacturing & Machinery (AREA)
• Polyamides (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Cosmetics (AREA)
• Medicinal Preparation (AREA)
• Paints Or Removers (AREA)
• Inks, Pencil-Leads, Or Crayons (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=38198356

Family Applications (1)

Country Status (11)

Families Citing this family (24)

Family Cites Families (9)

• 2006
  • 2006-12-28 FR FR0656024A patent/FR2910900B1/fr active Active
• 2007
  • 2007-12-20 CN CN200780048787.7A patent/CN101578319B/zh active Active
  • 2007-12-20 US US12/521,082 patent/US20100113661A1/en not_active Abandoned
  • 2007-12-20 EP EP07871995A patent/EP2125932A2/fr not_active Withdrawn
  • 2007-12-20 BR BRPI0720716-6A2A patent/BRPI0720716A2/pt not_active IP Right Cessation
  • 2007-12-20 AU AU2007344279A patent/AU2007344279A1/en not_active Abandoned
  • 2007-12-20 MX MX2009007035A patent/MX2009007035A/es unknown
  • 2007-12-20 WO PCT/FR2007/052584 patent/WO2008087335A2/fr active Application Filing
  • 2007-12-20 JP JP2009543507A patent/JP5394254B2/ja active Active
  • 2007-12-20 KR KR1020097013254A patent/KR101487034B1/ko active IP Right Grant
  • 2007-12-20 RU RU2009128969/04A patent/RU2009128969A/ru not_active Application Discontinuation

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events