Classifications

• • 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
  • C08F2/00—Processes of polymerisation
  • C08F2/01—Processes of polymerisation characterised by special features of the polymerisation apparatus used
• • 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
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
  • C08G18/6283—Polymers of nitrogen containing compounds having carbon-to-carbon double bonds
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J19/0006—Controlling or regulating processes
  • B01J19/0013—Controlling the temperature of the process
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J19/18—Stationary reactors having moving elements inside
  • B01J19/1862—Stationary reactors having moving elements inside placed in series
• • 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
  • C08F2/00—Processes of polymerisation
• • 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
  • C08F8/00—Chemical modification by after-treatment
  • C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
  • C08L33/04—Homopolymers or copolymers of esters
  • C08L33/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur, or oxygen atoms in addition to the carboxy oxygen
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
  • C09D133/04—Homopolymers or copolymers of esters
  • C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
  • C09D133/08—Homopolymers or copolymers of acrylic acid esters
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J2219/00002—Chemical plants
  • B01J2219/00027—Process aspects
  • B01J2219/00029—Batch processes
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J2219/00002—Chemical plants
  • B01J2219/00027—Process aspects
  • B01J2219/0004—Processes in series
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J2219/00049—Controlling or regulating processes
  • B01J2219/00051—Controlling the temperature
  • B01J2219/00054—Controlling or regulating the heat exchange system
  • B01J2219/00056—Controlling or regulating the heat exchange system involving measured parameters
  • B01J2219/00058—Temperature measurement
  • B01J2219/00063—Temperature measurement of the reactants
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J2219/00049—Controlling or regulating processes
  • B01J2219/00051—Controlling the temperature
  • B01J2219/00054—Controlling or regulating the heat exchange system
  • B01J2219/00056—Controlling or regulating the heat exchange system involving measured parameters
  • B01J2219/00065—Pressure measurement
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J2219/00049—Controlling or regulating processes
  • B01J2219/00051—Controlling the temperature
  • B01J2219/00074—Controlling the temperature by indirect heating or cooling employing heat exchange fluids
  • B01J2219/00087—Controlling the temperature by indirect heating or cooling employing heat exchange fluids with heat exchange elements outside the reactor
  • B01J2219/00094—Jackets
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J2219/00049—Controlling or regulating processes
  • B01J2219/00051—Controlling the temperature
  • B01J2219/00121—Controlling the temperature by direct heating or cooling
  • B01J2219/00123—Controlling the temperature by direct heating or cooling adding a temperature modifying medium to the reactants
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J2219/00049—Controlling or regulating processes
  • B01J2219/00051—Controlling the temperature
  • B01J2219/00121—Controlling the temperature by direct heating or cooling
  • B01J2219/0013—Controlling the temperature by direct heating or cooling by condensation of reactants
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J2219/00049—Controlling or regulating processes
  • B01J2219/00162—Controlling or regulating processes controlling the pressure
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J2219/00049—Controlling or regulating processes
  • B01J2219/00182—Controlling or regulating processes controlling the level of reactants in the reactor vessel
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J2219/02—Apparatus characterised by their chemically-resistant properties
  • B01J2219/025—Apparatus characterised by their chemically-resistant properties characterised by the construction materials of the reactor vessel proper
  • B01J2219/0277—Metal based
  • B01J2219/0286—Steel
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers

Definitions

• Such oligomers have been found very useful in producing low VOC (volatile organic component) coating compositions typically used in automotive OEM (original equipment manufacturer) and refinish applications.
• One method of achieving low molecular weight polymers is through the use of efficient chain transfer agents, but this approach has several drawbacks. This approach incorporates the structure of the chain transfer agent into the polymer chain. This can be undesirable since that structure will have an increasing effect on the properties of the polymer as molecular weight decreases.
• the chain transfer agents commonly employed are mercaptans. These materials are expensive and have objectionable odors associated with their presence.
• Other common chain transfer agents are hypophosphites, bisulfites and alcohols.
• the present invention is directed to a process for producing a polymer comprising: conveying hybrid reactor mixtures comprising one or more hybrid reactor monomers and one or more hybrid reactor initiators to one or more hybrid reactors maintained at effective hybrid polymerization temperatures and sub-reflux polymerization gage pressures to cause polymerization of a portion of said hybrid reactor monomers into said polymer; and conveying hybrid reactor contents to one or more batch reactors maintained at effective batch polymerization temperatures and reflux polymerization pressures to cause polymerization of a remaining portion of said hybrid reactor monomers into said polymer.
• the present invention is also directed to a process for producing a graft copolymer comprising: conveying hybrid reactor mixtures comprising one or more hybrid reactor monomers and one or more hybrid reactor initiators to one or more hybrid reactors maintained at effective hybrid polymerization temperatures and sub-reflux polymerization gage pressures to cause polymerization of said hybrid monomers into macromonomers; conveying hybrid reactor contents to one or more batch reactors maintained at effective batch polymerization temperatures and reflux polymerization pressures; and conveying batch reactor mixtures comprising one or more batch reactor monomers and one or more batch reactor initiators to cause polymerization of said batch reactor monomers into a backbone of said graft copolymer having said macromonomers grafted onto said backbones.
• the present invention is further directed to a polymerization system comprising: means for conveying hybrid reactor mixtures comprising one or more hybrid reactor monomers and one or more hybrid reactor initiators to one or more hybrid reactors; means for maintaining said hybrid reactors at effective hybrid polymerization temperatures and means for maintaining said hybrid reactors at sub-reflux polymerization gage pressures to cause polymerization of a portion of said hybrid reactor monomers into a polymer; means for conveying hybrid reactor contents from said hybrid reactors to one or more batch reactors; means for conveying batch reactor mixtures comprising one or more batch initiators to one or more batch reactors; and means for maintaining said batch reactors at effective batch polymerization temperatures and means for maintaining said batch reactors at reflux polymerization pressures to cause polymerization of remaining portion of said hybrid reactor monomers into said polymer.
• Figure 1 is a schematic representation of a preferred embodiment of a polymerization system of the present invention.
• Figures, 2, 3 and 4 are schematic representation of other embodiments of the polymerization system of the present invention- Detailed Description of Preferred Embodiment
• Polymer means homopolymer, copolymer, block copolymer; graft copolymer, comb copolymer, branched copolymer, branch-upon-branch copolymer, non-aqueous polymer dispersion, microgel, star polymer, oligomer, and ladder copolymer.
• oligomer refers to polymers having a degree of polymerization of 100 or less than 100, typically ranging from about 10 to 70.
• (Meth)acrylate means acrylate and methacrylate.
• GPC weight average molecular weight means a weight average molecular weight measured by utilizing gel permeation chromatography. A high performance liquid chromatograph (HPLC) supplied by Hewlett- Packard, Palo Alto, California was used. Unless stated otherwise, the liquid phase used was tetrahydrofuran and the standard was polymethyl methacrylate or polystyrene. "Tg” (glass transition temperature) measured in °C determined by DSC (Differential Scanning Calorimetry).
• Macromonomer means repeat units (mers) of limited chain length or molecular weight, which have such terminal olefinic moieties.
• terminal olefinic moieties is meant a vinyl molecule comprising (i) carboxylic acid or amide, or (ii) an ester or unsubstituted aryl as well as a moiety selected from epoxy, hydroxy, isocyanato, amino, anhydride, amide, carboxylic acid, silyl, cyano, and halo.
• the present macromonomers have about 10 to about 800 repeat units linked to the end group. In some cases, for reasons of commercial applicability and/or ease of synthesis, macromonomers having at least 10 and up to about 300 repeat units are preferred.
• the GPC number average molecular weight of the macromonomers can vary from about 1000 to 50,000, preferably 1 ,000 to 10,000.
• Polymerization medium means a liquid phase in which polymerization of monomers initiated by initiators takes place. Typically, the monomers and initiators are solvated or dispersed in the polymerization medium before polymerization. Often, the monomer mixture is solvated in the polymerization medium, either in one or more organic solvents, aqueous medium or a polymeric component, such as a polymer solvated or dispersed in the organic solvent or aqueous medium. If the monomer and resulting polymer are soluble in the medium, homogeneous polymerization takes place.
• the polymerization medium can include one or more organic solvents, an aqueous medium, or a polymeric component.
• Suitable organic solvents include acetone, methyl amyl ketone, methyl ethyl ketone, Aromatic 100 from ExxonMobil Chemical, Houston, Texas known as an aromatic solvent blend, xylene, toluene, ethyl acetate, n-butyl acetate, t-butyl acetate, butanol, and glycol ether, such as diethylene glycol monobutyl ether.
• Typical aqueous polymerization medium can include water or an aqueous solution of water and miscible solvents, such as ethanol, methyl ethyl ketone, propanol, glycol ether, n-methylpyrrolidone or a combination thereof.
• the polymeric component can include polyester, acrylic polymer, or a mixture thereof solvated or dispersed in one or more of the aforedescribed organic solvents or aqueous medium.
• the polyester suitable for use in the present invention can have a GPC weight average molecular weight exceeding 1500, preferably in the range of from 1500 to 100,000, more preferably in the range of 2000 to 50,000, still more preferably in the range of 2000 to 8000 and most preferably in the range of from 2000 to 5000.
• the Tg of the polyester can vary in the range of from - 50°C to +100°C, preferably in the range of from -20°C to +50°C.
• a blend of the polymeric medium containing, for example, polyester, and polymer of the present invention can be produced in situ by the polymerization process of the present invention.
• concentration of the monomer mixture in the reaction mixture can range from 70 to 100 weight percent.
• concentration can range from 40 to 90 weight percent.
• the concentration can range from 10 to 70 weight percent. All the foregoing weight percentages are based on the total weight of the reaction mixture.
• FIG. 1 illustrates a polymerization system 1 of the present invention, which includes one or more hybrid reactor systems 2 connected to one or more batch reactor systems 3 to make a polymer.
• Hybrid reactors system 2 includes one or more hybrid reactors 10.
• hybrid reactor 10 is made of a chemically inert material, such as stainless steel, and is rated to operate at sub-reflux gage pressures. The size of reactor 10 is chosen to meet the desired rate of making the polymer.
• Reactor 10 is provided with a conventional temperature probe 12, such as a thermocouple, for monitoring the temperature of a hybrid reactor reaction mixture comprising one or more hybrid reactor monomers and one or more hybrid reactor initiators in reactor 10.
• Reactor 10 is also provided with a conventional pressure probe, such as a load cell positioned in the dome of reactor 10 (not shown), for monitoring the pressure inside reactor 10.
• temperature probe 12 and the pressure probe are part of means for maintaining hybrid reactors 10 at effective hybrid polymerization temperatures and means for maintaining hybrid reactors 10 at sub-reflux polymerization gage pressures, respectively to cause polymerization of a portion or all of the hybrid reactor monomers into a polymer.
• the effective hybrid polymerization temperatures depend upon the type and quantity of hybrid reactor monomers, molar ratios of various monomers, type and amount of hybrid reactor initiators, type of polymerization medium, the rate at which the hybrid reactor mixture is added to reactor 10, rate at which hybrid reactor contents are taken out of reactor 10 and the sub-reflux polymerization gage pressures being maintained within reactor 10.
• effective hybrid polymerization temperatures range from 80°C to 400°C, preferably from 120°C to 300°C, and more preferably from 140°C to 220°C when sub-reflux polymerization gage pressures range from 0.1 to 2.86 MPa (0 to 400 psig), preferably from 0.1 to 0.71 MPa (0 to 100 psig).
• the hybrid operating pressures used in the present invention to make a polymer of a desired molecular weight range are far less than what has been tried before. As a result, the process of the present invention can be operated under safer working conditions.
• Reactor 10 is preferably provided with means for detecting the mass of the hybrid reactor contents present in reactor 10 to generate a signal to indicate that reactor 10 has been filled to a preset level.
• any suitable level sensing device can be used, such as for example, two or more pressure monitors, such as load cells 14A and 14B, can be preferably positioned in a vapor space 11 and preferably near the bottom of reactor 10, respectively.
• a pressure differential ( ⁇ P) between load cells 14 A and 14 B can be constantly monitored and a change in ⁇ P would • indicate that the preset level has been reached, at which point means for generating signal can generate a signal to start opening a controllable valve 30 to convey an excess portion of the hybrid reactor contents to batch reactor system 3.
• the means for generating signal can generate a signal to stop the flow of the hybrid reactor contents to batch reactor system 3 by closing controllable valve 30.
• the means for generating signal can also generate a signal to start replenishing of hybrid monomer mixtures, hybrid initiators and polymerization medium from means 22, 24 and 26, respectively into reactors 10 so that the preset level of volume can be maintained.
• Re.actor 10 is further provided with means 16 for heating, which typically include a heating jacket through which heat transfer medium, such as heated oil, can be passed through.
• a signal to increase or reduce the temperature of the heating medium is typically generated on the basis of preset polymerization conditions, which are dynamically controlled and monitored by temperature probe 12. It should be noted that polymerization temperatures could be profiled in accordance with a preset polymerization conditions, •
• Reactor 10 is preferably provided with a pressure relief device 18, such as a rupture disk, which can be set at a desired emergency hybrid reactor pressure.
• pressure relief device 18 opens rapidly to safely and rapidly relieve the hybrid reactor pressure by rapidly dumping the hybrid reactor contents into batch reactor system 3 or inte ⁇ a separate dump tank (not shown).
• Pressure relief device 18 is typically set at 50% of the design pressure of hybrid reactor 10.
• Reactor 10 is preferably provided with means 20 for agitating the hybrid reactor contents to provide thorough mixing of the hybrid reactor contents.
• One typical means 20 include a stirrer rotated at a desired rotation speed varied in accordance with a degree of mixing desired. Additionally, fixed baffles (not shown) may be provided on the reactor walls of reactor 10 to further improve the degree of mixing.
• Reactor 10 is provided with means 22 for conveying hybrid reactor mixtures comprising one or more hybrid reactor monomers and means 24 for conveying one or more hybrid reactor initiators to one or more hybrid reactors 10.
• means 22 and 24 include conventional means 22A and 24A for pumping the hybrid reactor monomers and the hybrid reactor initiators, respectively under pressure to reactor 10.
• Means 22 and 24 further include one or more tanks for storing monomers and initiators, which can be solvated or dispersed in a polymerization medium, described below, before they are conveyed to reactor 10.
• Reactor 10 is preferably provided with means 26 for conveying a polymerization medium to convey the polymerization medium to reactor 10.
• means 26 include conventional means 26A for pumping the polymerization medium under pressure to reactor 10.
• Means 26 further include one or more tanks for storing the polymerization medium.
• Reactor 10 is preferably provided with a condenser 28, which is preferably vertically mounted, for condensing of and retuning of any vapor phase back to reactor 10.
• Reactor 10 is operated at constant preset hybrid reactor pressures or pressures that are profiled in accordance with a preset polymerization conditions.
• One of the ways to achieve such conditions is by controlled venting of vapor space 11 through a controlled valve 29 A and pumping in inert gas at a desired pressure, such as nitrogen, argon, carbon dioxide, or a mixture thereof, through controlled valve 29 B in vapor space 11.
• the use of inert gas is preferred to prevent undesired reactions from occurring in reactor 10.
• Reactor 10 is further provided with controllable valve 30 to convey the hybrid reactor contents to batch reactor system 3 of the present invention.
• Figure 1 illustrates hybrid reactor connected to a batch reactor 32, via valve 30.
• the volume of hybrid reactor 10 is calculated on the basis of the throughput of the polymer desired. Due to high pressures and temperatures, the rate of polymerization in hybrid reactor 10 is generally higher than that taking place in batch reactor 32. As a result, generally the volume of hybrid reactor 10 is less than that of batch reactor 32 and it generally varies from 1% to 90%, preferably from 5% to 50% and more preferably from 10% to 40% of the total volume of batch reactor 32.
• Typical sizes of batch reactor 32 can range from 1 liter (0.26 gallons) to 75,700 liters (20,000 gallons).
• Hybrid reactor 10 is preferably positioned above batch reactor 32 to gravimetrically assist in conveying the hybrid reactor contents to batch reactor 32. However, it is within the purview of this invention to position hybrid reactor 10 in any advantageous position with respect to batch reactor 32, including providing pumping means to facilitate in the conveying the hybrid reactor contents from hybrid reactor 10 to batch reactor 32.
• Batch reactor 32 is made of a chemically inert material, such as stainless steel, and is rated to operate at reflux gage pressures, which is typically at atmospheric pressure- The size of reactor 32 is chosen to meet the desired rate of making the polymer as discussed above.
• Reactor 32 is provided with a conventional temperature probe 34, such as a thermocouple, for monitoring the temperature of a batch reactor reaction mixture comprising one or more batch reactor monomers and one or more batch reactor initiators in reactor 32.
• Reactor 32 is also provided with a conventional pressure probe, such as a load cell positioned in the dome of reactor 32 (not shown), for monitoring the pressure inside reactor 32.
• temperature probe 34 and the pressure probe are part of means for maintaining batch reactors 32 at effective batch polymerization temperatures and means for maintaining batch reactors 32 at reflux polymerization gage pressures, respectively to cause polymerization of a remaining portion of the hybrid reactor monomers into the polymer and to cause polymerization of batch reactor monomers into the polymer.
• the effective batch polymerization temperatures depend upon the type and quantity of hybrid reactor and batch reactor monomers, molar ratios of various monomers, type and amount of batch reactor initiators, type of polymerization medium, the rate at which the hybrid reactor content are conveyed to reactor 32, the rate at which batch reactor mixture is added to reactor 32, and the reflux polymerization gage pressures being maintained within reactor 32.
• effective batch polymerization temperatures range from 80°C to 300°C, preferably from 100°C to 250°C, and more preferably from 120°C to 200°C when reflux polymerization gage pressures range from 0.1 to 2.17 MPa (0 to 300 psig), preferably from 0.1 to 0.79 MPa (0 to 100 psig).
• Batch reactor 32 is further provided with means 36 for heating, which typically includes a heating jacket through which heat transfer medium, such as oil, can be passed through.
• a signal to increase or reduce the temperature of the heating medium is typically generated on the basis of preset polymerization conditions, which are dynamically controlled and monitored by temperature probe 34- It should be noted that polymerization temperatures could be profiled in accordance with a preset polymerization conditions.
• Reactor 32 is preferably provided with a pressure relief device 50, such as a rupture disk, which can be set at a desired emergency hybrid reactor pressure. Thus, if a severe runaway reaction condition occurs in reactor 32, which can occur very rapidly, pressure relief device 18 opens rapidly to safely and rapidly relieve the hybrid reactor pressure and dump the batch reactor contents in a dump tank (not shown).
• Reactor 32 is preferably provided with means 38 for agitating the batch reactor contents to provide thorough mixing of the batch reactor contents.
• One typical means 38 include a stirrer rotated at a- desired rotation speed varied in accordance with a degree of mixing desired. Additionally, fixed baffles (not shown) may be provided on the reactor walls of reactor 32 to further improve the degree of mixing.
• Reactor 32 is provided with means 40 for conveying batch reactor mixtures comprising one or more batch reactor monomers and means for conveying 42 one or more batch reactor initiators to one or more batch reactors 32.
• Means 40 and 42 further include one or more tanks for storing monomers and initiators, which can be solvated or dispersed in a polymerization medium, described below, before they are conveyed to reactor 32.
• Reactor 32 is preferably provided with means 44 for conveying a polymerization medium to convey the polymerization medium to reactor 32.
• Means 44 further include one or more tanks for storing the polymerization medium.
• means 40, 42 and 44 could be provided with conventional pumping means.
• Reactor 32 is preferably provided with a condenser 46, which is preferably vertically mounted, for condensing of and returning of any vapor phase back to reactor 32.
• Reactor 32 is operated at reflux pressures.
• One of the ways to achieve such conditions is by controlled venting of vapor space 33 by pumping in the aforedescribed inert gas into vapor space 33. The use of inert gas under a desired pressure is preferred to prevent undesired reactions from occurring in reactor 33.
• the contents of the batch reactor are conveyed via a controllable valve 48 into a holding tank for further processing such as making a composition, such as a coating composition suitable for use in automotive OEM or refinish applications.
• the present invention is preferably directed to a single hybrid reactor 10 connected to a single batch reactor 32. Additionally, all the monomers to be polymerized are preferably conveyed to hybrid reactor 10, batch reactor 32 being used to complete the polymerization of any remaining unpolymerized hybrid reactor monomers present in the hybrid reactor contents by preferably using the same or similar type of hybrid reactor initiator as a batch reactor initiator.
• the polymerization medium is preferably conveyed to hybrid reactor 10 before the hybrid reactor mixture is conveyed and the polymerization medium is preferably conveyed to batch reactor 32 after the hybrid reactor contents conveyed to batch reactor 32.
• the polymerization medium is preferably brought to effective hybrid polymerization temperatures and sub-reflux polymerization gage pressures before the hybrid reactor mixture is conveyed.
• the polymerization medium is preferably brought to effective batch polymerization temperatures and reflux polymerization gage pressures once the hybrid reactor contents are conveyed to batch reactor 32.
• Figure 2 illustrates another embodiment of the polymerization system of the present invention. Unless otherwise noted, all the components not referenced will be similar to those illustrated in Figure 1 and described earlier.
• the polymerization system of Figure 2 includes: means for conveying first hybrid reactor mixtures comprising one or more first hybrid reactor monomers and one or more first hybrid reactor initiators to a first hybrid reactor 10A; means for maintaining first hybrid reactor 10A at effective first hybrid polymerization temperature and means for maintaining first hybrid reactor 10A at first sub-reflux polymerization gage pressure to cause polymerization of a portion of said first hybrid reactor monomers into a polymer; means for conveying second hybrid reactor mixtures comprising one or more second hybrid reactor monomers and one or more second hybrid reactor initiators to a second hybrid reactor 10B; means for maintaining second hybrid reactor 10B at effective second hybrid polymerization temperature and means for maintaining second hybrid reactor 10B at second sub-reflux polymerization gage pressure to cause polymerization of another portion of said first hybrid reactor monomers and a portion of said second hybrid reactor monomers into said polymer; means for conveying first hybrid reactor contents from first hybrid reactor 10A to a batch reactor 32A; means for conveying second hybrid reactor contents from second hybrid reactor 10B to batch reactor 32A
• Figure 3 illustrates another embodiment of the polymerization system of the present invention. Unless otherwise noted, all the components not referenced will be similar to those illustrated in Figure 1 and described earlier.
• the polymerization system of Figure 3 includes: means for conveying hybrid reactor mixtures comprising one or more hybrid reactor monomers and one or more hybrid reactor initiators to a hybrid reactor 10C; means for maintaining hybrid reactor 10C at effective hybrid polymerization temperature and means for maintaining hybrid reactor 10C at sub-reflux polymerization gage pressure to cause polymerization of a portion of said hybrid reactor monomers into a polymer; means for conveying portions of hybrid reactor contents from hybrid reactor 10C to a first batch reactor 32B and a second batch reactor 32C; means for conveying first batch reactor mixture comprising one or more batch initiators to first batch reactor 32B; means for conveying second batch reactor mixture comprising one or more batch initiators to second batch reactor 32C; means for maintaining first batch reactor 32B at effective first batch polymerization temperature and means for maintaining first batch reactor 32B at reflux polymerization pressure to cause polymerization
• FIG 4 illustrates still another embodiment of the polymerization system of the present invention. Unless otherwise noted, all the components not referenced will be similar to those illustrated in Figure 1 and described earlier.
• the polymerization system of Figure 3 includes: means for conveying first hybrid reactor mixtures comprising one or more first hybrid reactor monomers and one or more first hybrid reactor initiators to a first hybrid reactor 10D; means for maintaining first hybrid reactor 10D at effective first hybrid polymerization temperature and means for maintaining said first hybrid reactor at first sub-reflux polymerization gage pressure to cause polymerization of a portion of said first hybrid reactor monomers into a polymer; means for conveying first hybrid reactor contents from first hybrid reactor 10D to a second hybrid reactor 10E; means for conveying second hybrid reactor mixtures comprising one or more second hybrid reactor monomers and one or more second hybrid reactor initiators to second hybrid reactor 10E; means for maintaining second hybrid reactor 10E at effective second hybrid polymerization temperature and means for maintaining second hybrid reactor 10E at second sub-reflux polymerization gage pressure to cause polymerization of another portion
• the polymerization systems of Figures 1 , 2, 3 and 4 can be used to make polymers in the form of a homopolymer, copolymer, block polymer, graft or comb copolymer, branched polymer, branch-upon-branch polymer, non-aqueous polymer dispersion, star polymer, and ladder polymer.
• the present invention is also directed to a process for producing a polymer comprising the following steps: I.
• hybrid reactor mixtures comprising one or more hybrid reactor monomers and one or more hybrid reactor initiators, respectively to one or more hybrid reactors 10A maintained at effective hybrid polymerization temperatures and sub- reflux polymerization gage pressures to cause polymerization of a portion of said hybrid reactor monomers into said polymer.
• the portion of the hybrid monomers polymerized in hybrid reactors 10 ranges from 30 weight percent to 99 weight percent, preferably from 50 weight percent to 90 weight percent and preferably from 60 weight percent to 85 weight percent, all percentages based on the total amount of hybrid monomers conveyed to hybrid reactors 10.
• the hybrid reactor mixture can contain a polymerization medium described earlier.
• effective polymerization temperatures are maintained by monitoring the temperature of the contents of the hybrid reactor 10A by hybrid reactor temperature probe 12 and then increasing or lowering the heat provided means 16 for heating in accordance with a preset polymerization temperature.
• the polymerization medium is preferably conveyed to hybrid reactors 10 before the hybrid reactor mixtures are conveyed to hybrid reactor 10.
• an excess portion of the hybrid reactor contents can be conveyed to batch reactors 32 once hybrid reactors 10 are filled to preset levels.
• the maintenance of the present levels in hybrid reactor 10 can be achieved by utilizing the following process steps: detecting the mass reactor contents present in hybrid reactors 10 and generating signal to open controllable valve 30 to convey of an excess portion of the hybrid reactor contents to batch reactor system 3.
• the portion of the hybrid reactor monomers polymerized in hybrid reactors 10 ranges from 30 weight percent to 99 weight percent, preferably ranges from 50 weight percent to 90 weight percent and more preferably ranges from 60 weight percent to 85 weight percent, all based on the total amount of hybrid reactor monomers conveyed to hybrid reactors 10.
• hybrid/batch reactor combination of the present invention By utilizing hybrid/batch reactor combination of the present invention, for the same throughput of the polymer produced, one can reduce the time of polymerization typically by an hour to two hours, since the time required to heat a single conventional larger size batch reactor to polymerization temperatures would be longer than a smaller size hybrid reactor 10. If desired, a solution of the hybrid reactor initiators in the polymerization medium is conveyed to hybrid reactors 10.
• Typical monomers suitable for use in the hybrid reactor mixture or batch reactor mixtures include one or more of the following: One or more acrylate monomers having alkyl carbon atoms in the range of from 1 to 18, preferably in the range of from 1 to 12.
• suitable acrylate monomers include methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate, butyl (meth)acrylate, 2- ethylhexyl (meth)acrylate, isobutyl (meth)acrylate, isobomyl (meth)acrylate, benzyl (meth)acrylate, and phenyl (meth)acrylate.
• One or more functional acrylic monomers such as glycidyl meth)acrylate, 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, 3-hydroxypropyl (meth)acrylate, hydroxybutyl meth)acrylate, diethylaminoethyl (meth)acrylate, triethyleneglycol (meth)acrylate, diethylaminoethyl (meth)acrylate, and triethyleneglycol (meth)acrylate.
• One or more acid monomers such as (meth)acrylic acid, itaconic acid, vinyl benzoic acid, alphamethylvinyl benzoic acid, and p-vinyl benzene sulfonic acid.
• Nitrile monomers such as (meth)acrylonitrile.
• Styrene and one or more styrenic monomers such alpha methyl styrene, diethylamino styrene, diethylamino alphamethylstyrene, and para- methylstyrene.
• One or more amides such as methacrylamide, N-tert-butyl methacrylamide, N-n-butyl methacrylamide, N-methylol methacrylamide, N-ethylol methacrylamide, N-tert-butyl acrylamide, N-n-butyl acrylamide, N-methylol acrylamide, and N-ethylol acrylamide.
• silyl monomers such as trimethoxysilylpropyl (meth)acrylate, triethoxysilylpropyl (meth)acrylate, tributoxysilylpropyl (meth)acrylate, dimethoxymethylsilylpropyl (meth)acrylate, diethoxymethylsilylpropyl (meth)acrylate, dibutoxymethylsilylpropyl (meth)acrylate, diisopropoxymethylsilylpropyl (meth)acrylate, dimethoxysilylpropyl (meth)acrylate, diethoxysilylpropyl (meth)acrylate, dibutoxysilylpropyl (meth)acrylate, and diisopropoxysilylpropyl (meth)acrylate.
• silyl monomers such as trimethoxysilylpropyl (meth)acrylate, triethoxysilylpropyl (meth)acrylate, tributoxysilylpropyl (meth)
• One or more vinyl monomers such as vinyl silane, vinyl acetate, vinyl butyrate, vinyl chloride, vinyl fluoride, and vinyl bromide.
• Typical initiators suitable for use in the hybrid reactor mixture or batch reactor mixtures include one or more of any source of radicals or any of the known class of polymerization initiators, provided the initiator has the requisite solubility in the solvent or monomer mixture chosen and has an appropriate half-life at the temperature of polymerization.
• the initiators may be redox initiators, thermal initiators, photochemical initiators, or a combination thereof.
• the thermal initiators are preferred, particularly, azo initiators, peroxide initiators, and persulfate initiators.
• the initiator has a half-life of from about 1 minute to about 1 hour at the temperature of polymerization.
• suitable initiators include ammonium persulfate, azocumene; 2,2'-azobis(isobutyronitrile) (Vazo ® 64 thermal initiator supplied by Du Pont Company, Wilmington, Delaware); 4,4'-azobis(4-cyanovaleric acid) (Vazo ® 52 thermal initiator supplied by Du Pont Company, Wilmington, Delaware) and 2-(t-butylazo)-2- cyanopropane, benzoyl peroxide, t-butyl peroxyacetate, di-tertiary-butyl • peroxide, t-buyl peroxypivalate.
• Additional azo and peroxide initiators include 2,2'-azobis(isobutyronitrile), 2,2'-azobis(2-methylbutanenitrile), dimethyl 2,2'-azobis(methyl isobutyrate), 4,4'-azobis(4-cyanopentanoic acid), 4,4'-azobis(4-cyanopentan-1-ol), 1 ,1'- azobis(cyclohexanecarbonitrile), 2-(t-butylazo)-2-cyanopropane, 2,2'- azobis[2-methyl-N-(1 , 1 )-bis(hydoxymethyl)-2-hydroxyethyl] propionamide, 2,2'-azobis[2-methyl-N-hydroxyethyI)]-propionamide, 2,2'-azobis(N,N'- dimethyleneisobutyramidine) dihydrochloride, 2,2'-azobis(2- amidinopropane) dihydrochloride, 2,2'-azobis(N,N'- dim
• non-azo initiators having the requisite solubility and appropriate half-life may also be used. Typical quantities of initiator used ranges from 0.1. weight percent to 10 weight percent based on total weight of monomers in the reaction mixture.
• the process of the present invention can be readily run in a safe working manner by conveying a portion or all of the hybrid reactors contents from hybrid reactors 10 to batch reactors 32, if the pressures in hybrid reactors 10 exceed above a preset unsafe hybrid reactor pressures, described earlier.
• the process further includes rinsing hybrid reactors 10 with a chaser portion of the polymerization medium after all of the hybrid reactor . contents had been conveyed to batch reactors 32; and then conveying the chaser portion to batch reactors 32.
• the process of the present invention produces a polymer, particularly acrylic polymer polymerized from one or a combination of (meth)acrylic monomers, acrylonitriles, acrylamides, styrenic monomers, and vinyl silane.
• the acrylic polymer can have a GPC weight average molecular weight exceeding 5000, preferably in the range of from 5000 to 20,000, more preferably in the range of 6000 to 20,000, and most preferably in the range of from 8000 to 12,000.
• the Tg of the acrylic polymer varies in the range of from 0°C to 100°C, preferably in the range of from 30°C to 80°C.
• the polymer made by the process of the present invention is suited for use in coating compositions, such as OEM and refinish coating compositions used in automotive applications.
• the process of the present invention can be also used for producing a graft copolymer.
• Such a process includes the following steps: I. Conveying hybrid reactor mixtures comprising one or more hybrid reactor monomers and one or more hybrid reactor initiators to one or more hybrid reactors 10 maintained at effective hybrid polymerization temperatures and sub-reflux polymerization gage pressures to cause polymerization of said hybrid monomers into macromonomers. II. Conveying hybrid reactor contents to one or more batch reactors 32 maintained at effective batch polymerization temperatures and reflux polymerization pressures. III.
• Conveying batch reactor mixtures comprising one or more batch reactor monomers and one or more batch reactor initiators to cause polymerization of said batch reactor monomers into a backbone of said graft copolymer having said macromonomers grafted onto said backbones.
• the foregoing graft copolymer process includes conveying on or more chain transfer catalysts to provide said macromonomers with an unsaturated terminal group.
• the chain transfer agent can be any compound, which contains CO +2 .
• Cobalt chelates are preferred, especially those described in U.S. Pat. No. 4,680,352 to Janowicz and Melby and U.S. Pat. No. 4,722,984 to Janowicz. Most preferred are pentacyanocobaltate (II) diaquabis(borondi fiuorodi methylglyoximato)cobal tate (II) and diaquabis(borondifluorodiphenylglyoximato)cobaltate.
• the chain transfer agent is generally used at concentration of about 5 to 150 weight parts per million based on the total weight of the monomer mixture.
• the hybrid reactor contents and the batch reactor mixtures are preferably conveyed simultaneously to batch reactors 32 or the hybrid reactor contents are preferably conveyed to batch reactors 32 after the conveying of a portion or all of the batch reactor monomers to batch reactors 10.
• a portion or all of the batch reactor initiators is preferably conveyed simultaneously with the batch reactor monomers or with the hybrid reactor contents to batch reactors 32.
• the foregoing graft copolymer process preferably includes conveying the polymerization medium to hybrid reactors 10, batch reactors 32; or to both before conveying the hybrid reaction mixtures to hybrid reactors 10.
• the foregoing graft copolymer process preferably includes conveying the polymerization medium to hybrid reactors 10 before conveying the hybrid reaction mixtures to hybrid reactors 10.
• the foregoing graft copolymer process preferably includes conveying the polymerization medium to batch reactors 32 before conveying the hybrid reactor contents to batch reactors 32.
• the foregoing graft copolymer process preferably includes conveying the polymerization medium to batch reactors 32 before conveying the batch reactor mixtures to batch reactors 32.
• the foregoing graft copolymer process preferably includes conveying the polymerization medium to batch reactors 10 before conveying the batch reactor mixtures and the hybrid reactors contents to batch reactors 10.
• a solution of the hybrid reactor initiators in a portion of the polymerization medium could be conveyed to hybrid reactors 10.
• a solution of the batch reactor initiators in a portion of the polymerization medium could be conveyed to batch reactors 32.
• a solution of the hybrid reactor initiators in a portion of the polymerization medium can be conveyed to hybrid reactors 10; and a solution of the batch reactor initiators in another portion of the polymerization medium can be conveyed to batch reactors 32.
• the foregoing process could be also used for producing block copolymers.
• the process of the present invention can be also used for producing a polymer blend.
• Such a process includes: conveying the hybrid reactor mixtures comprising one or more hybrid reactor monomers and one or more hybrid reactor initiators to one or more hybrid reactors 10 maintained at effective hybrid polymerization temperatures and sub-reflux polymerization gage pressures to cause polymerization of the hybrid monomers into a hybrid reactor polymer; conveying hybrid reactor contents to one or more batch reactors 32 maintained at effective batch polymerization temperatures and reflux pressures; and conveying batch reactor mixtures comprising one or more batch reactor monomers and one or more batch reactor initiators to cause polymerization of the batch reactor monomers into a batch reactor polymer to form the polymer blend of the hybrid reactor polymer and the batch reactor polymer.
• the polymers made according to the present invention have wide utility, especially for use as binders in coating compositions (particularly high performance coatings used in automotive finishes and industrial maintenance coating compositions), inks, adhesives, and sealants, or basically wherever one skilled in the art would use polymeric material.
• Such final products or compositions can have advantageous structural characteristics and properties associated with the use of the present polymers.
• the graft copolymers, comb copolymers, oligomers, block copolymers prepared according to the present invention can be used to improve coating properties, such as, for example improved VOC (by lowering the content of volatile organic compounds), better crosslink density, better pot life, better environmental resistance, faster cure, and improved hardness.
• the coating composition can be made conventionally by mixing the polymer of the present invention with conventional composition additives, such as, pigments, metallic flakes, hollow glass beads, UV absorbers, stabilizers, rheology control agents, flow agents, reinforcing fibers, toughening agents and fillers.
• additives such as, pigments, metallic flakes, hollow glass beads, UV absorbers, stabilizers, rheology control agents, flow agents, reinforcing fibers, toughening agents and fillers.
• additional additives will, of course, depend upon the intended use of the coating composition. Fillers, pigments, and other additives that would adversely affect the clarity of the cured coating are typically not included if the composition is intended as a clear coating.
• the present invention is also suitable for producing microgels, which are macromolecules that possess a very high molecular weight and yet a low viscosity similar to linear or branched polymers of relatively low " molecular weight.
• Microgels are an intermediate structure between conventional linear or branched polymers such as polyethylene or polycarbonate and networks such as vulcanized natural rubber.
• the dimensions of microgels are comparable with high molecular weight linear polymers but their internal structure resembles a network.
• the properties of microgels make them particularly useful in a wide range of applications such as in additives, in advanced material formulations for foams or fibers, in coating compositions, binders and redispersible polymers.
• Microgels can also be used to improve the ease of processing and to improve the structural strength and dimensional stability of the final products.
• a further potential use for microgels is as additives for high impact polymers.
• Microgels embedded in a matrix of conventional linear polymer can act to stabilize the whole structure by distributing mechanical tension.
• Microgels are also useful in biological systems and as pharmaceutical carriers.
• Examples Comparative Copolymer 1 To a 2-liter flask fitted with an agitator, water condenser, thermocouple, nitrogen inlet, heating mantle, and addition pumps and ports was added 305.3 g. of xylene supplied by ExxonMobil, Houston, Texas, which was agitated and heated to reflux temperature (137°C to 142°C). A monomer mixture comprising of 106.1 g of styrene (Styrene from BP Amoco, Texas City, Texas), 141.4 g.
• methyl methacrylate (MMA from Lucite International, Inc. Cordova, Tennessee), 318.3 g. iso-butyl methacrylate (I-205 from Lucite International, Inc. Cordova, Tennessee), 141.4 g. hydroxyethyl methacrylate (Rorcryl ® 400 from Rohm and Haas Company, Philadelphia, PA) and 10.4g of xylene supplied by ExxonMobil, Houston, Texas was then added to the flask via the addition pumps and ports simultaneously with an initiator mixture comprising 17.0 g. t-butyl peracetate (Luperox ® 7M75 initiator from Atofina, Philadelphia,
• the amount of the initiator solution used was 3.0 weight percent based on the total weight of the monomer mixture.
• the resulting polymer solution has weight solids of 60% and viscosity of 14,400 cps.
• the number average molecular weight of the resulting hydroxy functional acrylic copolymer was 5,000 and weight average molecular weight was 11 ,000, as determined by gel permeation chromatography (polystyrene standard).
• Copolymer 1 To 1 -liter hybrid reactor 10 fitted with heating jacket 16, stirrer 20, feed lines from means 22 for conveying hybrid reactor monomers, means 24 for conveying hybrid reactor initiator, and means 26 for conveying polymerization medium, an initial polymerization medium charge of 355.0 g.
• MMA methyl methacrylate
• I-205 iso-butyl methacrylate
• 88.2 g. of xylene supplied by ExxonMobil, Houston, Texas as solvent was added to reactor 10 over a period of 240 minutes in such a way that the level in the reactor 10 was held constant at 0.55 liters and an excess portion of the hybrid reactor contents was fed to an attached 12-liter batch reactor 32 fitted with heating jacket 36, stirrer 38, water cooled condenser with nitrogen purge 46 and a feed line from means 44 for conveying batch reactor initiator.
• a hybrid initiator mixture of 27.7g of tert- butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 24 and 1063.4g of xylene supplied by ExxonMobil, Houston, Texas from means 26 was added over a period of 240 minutes to reactor 10 under sub-reflux at 54.7 psia (0.38 MPa).
• a polymerization temperature of 190°C was maintained in reactor 10 over the entire reaction time. After completion of the feeds to reactor 10, it was drained over 25 minutes into reactor 32. Once transfer from reactor 10 to reactor 32 began, reactor 32 was heated to reflux at 140°C.
• a batch initiator mixture of 0.9 g. of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 42 and 18.2 g. of xylene supplied by ExxonMobil, Houston, Texas from means 44 were added all at once to reactor 32.
• another batch initiator mixture of 8-3 g. of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 42 and 171.2 g. of xylene supplied by ExxonMobil, Houston, Texas from means 44 were fed to reactor 32 over 230 minutes.
• the resulting copolymer @ 60.5 % solids had a GPC Mn of 5512 and GPC Mw of 10997 using a polystyrene standard.
• Copolymer 1 to Comparative Copolymer that for producing a polymer having substantially similar molecular weights, the process of the present invention utilizes just about half the amount of initiator (1.6% versus 3.0%).
• Copolymer 2 To 1 -liter hybrid reactor 10 fitted with heating jacket 16, stirrer 20, feed lines from means 22 for conveying hybrid reactor monomers, means 24 for conveying hybrid reactor initiator, and means 26 for conveying polymerization medium, an initial polymerization medium charge of 348.6g of 2-heptanone (methyl amyl ketone from Eastman Chemical, Kingsport, Tennessee) was added from means 26. The polymerization medium was heated to 190°C under sub-reflux at 54.7 psia (0.38 MPa) in reactor 10. A hybrid monomer mixture of 1138.2g of hydroxy ethyl methacrylate (Rorcryl ® 400 from Rohm and Haas Co., Philadelphia, Pennsylvania), 1938.
• Rorcryl ® 400 hydroxy ethyl methacrylate
• Og of isobornyl acrylate (SR-506 isobornyl acrylate from Sartomer Resin, Channelview, Texas) and 82.
• Og of 2-heptanone (methyl amyl ketone from Eastman Chemical, Kingsport, Tennessee) 462.4g as solvent was added to reactor 10 over a period of 280 minutes in such a way that the level in the reactor 10 was held constant at 0.55 liters and an excess portion of the hybrid reactor contents was fed to an attached 12-liter batch reactor 32 fitted with heating jacket 36, stirrer 38, water cooled condenser with nitrogen purge 46 and a feed line from means 44 for conveying batch reactor initiator.
• a hybrid initiator mixture of 92.3g of tert- butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 24 and 1045.9g of 2-heptanone (methyl amyl ketone from Eastman Chemical, Kingsport, Tennessee) from means 26 was added over a period of 280 minutes to reactor 10 under sub-reflux at 54.7 psia (0.38 MPa) in reactor 10. Polymerization temperature of 190°C was maintained in reactor 10 over the entire reaction time. After completion of the feeds to reactor 10, it was drained over 25 minutes into reactor 32. Once transfer from reactor 10 to reactor 32 began, reactor 32 was heated to reflux at 157°C.
• a batch initiator mixture of 9.2g of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 42 and 38.9g of 2- heptanone (methyl amyl ketone from Eastman Chemical, Kingsport, Tennessee) from means 44 were added all at once to reactor 32.
• another batch initiator mixture of 83.1 g of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 42 and 350.7g of 2-heptanone (methyl amyl ketone from Eastman Chemical, Kingsport, Tennessee) from means 44 were fed to reactor 32 over 270 minutes.
• the amount of the initiator solution used was 6.0 weight percent based on the total weight of the monomer mixture.
• the reactor 32 was held at reflux for 1 hour and cooled to 80°C and the batch filled out.
• the resulting copolymer @ 60.5 % solids had a GPC Mn of 1704 and GPC Mw of 3380 using a polystyrene standard.
• Copolymer 3 To 1 -liter hybrid reactor 10 fitted with heating jacket 16, stirrer 20, feed lines from means 22 for conveying hybrid reactor monomers, means 24 for conveying hybrid reactor initiator, and means 26 for conveying polymerization medium, an initial polymerization medium charge of 268-4g of xylene supplied by ExxonMobil, Houston, Texas was added from means 26.
• the polymerization medium was heated to 190°C under sub-reflux at 54.7 psia (0.38 MPa) in reactor 10.
• a hybrid monomer mixture of 2489.9g of isobutyl methacrylate (IBMA from Lucite International, Inc., Cordova, Tennessee), 1067.1g of hydroxy ethyl acrylate (Rocryl ® 420 HEA from Rohm and Haas, Philadelphia, Pennsylvania) and 33.3g of xylene supplied by ExxonMobil, Houston, Texas as solvent was added to reactor 10 over a period of 240 minutes in such a way that the level in the reactor 10 was held constant at 0.55 liters and an excess portion of the hybrid reactor contents was fed to an attached 12-liter batch reactor 32 fitted with heating jacket 36, stirrer 38, water cooled condenser with nitrogen purge 46 and a feed line from means 44 for conveying batch reactor initiator.
• a hybrid initiator mixture of 14.5g of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 24 and 803.4g of xylene supplied by ExxonMobil, Houston, Texas from means 26 was added over a period of 240 minutes to reactor 10 under sub-reflux at 54.7 psia (0.38 MPa) in reactor 10. Polymerization temperature of 190°C was maintained in reactor 10 over the entire reaction time. After completion of the feeds to reactor 10, it was drained over 25 minutes into reactor 32. Once transfer from reactor 10 to reactor 32 began, reactor 32 was heated to reflux at 140°C.
• a batch initiator mixture of 1.9g of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 42 and 12.0g of xylene supplied by ExxonMobil, Houston, Texas from me /ans 44 were added all at once to reactor 32.
• another batch initiator mixture of 17.5g of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 42 and 108.4g of xylene supplied by ExxonMobil, Houston, Texas from means 44 were fed to reactor 32 over 220 minutes.
• the Tg of the copolymer was -16.5°C, using dynamic scanning calorimetry.
• Copolymer 4 To 1 -liter hybrid reactor 10 fitted with heating jacket 16, stirrer 20, feed lines from means 22 for conveying hybrid reactor monomers, means 24 for conveying hybrid reactor initiator, and means 26 for conveying polymerization medium, an initial polymerization medium charge of 268.4g of xylene supplied by ExxonMobil, Houston, Texas was added from means * 26. The polymerization medium was heated to 190°C under sub-reflux at 54.7 psia (0.38 MPa) in reactor 10.
• IBMA isobutyl methacrylate
• 1067.1g hydroxy eth
• a hybrid initiator mixture of 14.5g of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 24 and 803.4g of xylene supplied by ExxonMobil, Houston, Texas from means 26 was added over a period of 240 minutes to reactor 10 under sub-reflux at 54.7 psia (0.38 MPa) in reactor 10. Polymerization temperature of 190°C was maintained in reactor 10 over the entire reaction time. After completion of the feeds to reactor 10, it was drained over 25 minutes into reactor 32. Once transfer from reactor 10 to reactor 32 began, reactor 32 was heated to reflux at 140°C.
• a batch initiator mixture of 1.9g of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 42 and 12.0g of xylene supplied by ExxonMobil, Houston, Texas from means 44 were added all at once to reactor 32.
• another batch initiator mixture of 17.5g of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 42 and 108.4g of xylene supplied by ExxonMobil, Houston, Texas from means 44 were fed to reactor 32 over 220 minutes.
• the polymerization medium was heated to 175°C under sub-reflux at 54.7 psia (0.38 MPa) in reactor 10.
• a hybrid monomer mixture of 2489.8g of isobornyl methacrylate (AGEFLEX ® IBOMA from CIBA Specialty Chemicals, High Point, North Carolina), 1067.1g of hydroxy ethyl acrylate (Rocryl ® 420 HEA from Rohm and Haas, Philadelphia, Pennsylvania) and 33.3g of xylene supplied by ExxonMobil, Houston, Texas as solvent was added to reactor 10 over a period of 240 minutes in such a way that the level in the reactor 10 was held constant at 0.55 liters and an excess portion of the hybrid reactor contents was fed to an attached 12-liter batch reactor 32 fitted with heating jacket 36, stirrer 38, water cooled condenser with nitrogen purge 46 and a feed line from means 44 for conveying batch reactor initiator.
• a hybrid initiator mixture of 14.5g of tert- butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 24 and 803.4g of xylene supplied by ExxonMobil, Houston, Texas from means 26 was added over a period of 240 minutes to reactor 10 under sub-reflux at 54.7 psia (0.38 MPa) in reactor 10. Polymerization temperature of 190°C was maintained in reactor 10 over the entire reaction time. After completion of the feeds to reactor 10, it was drained over 25 minutes into reactor 32. Once transfer from reactor 10 to reactor 32 began, reactor 32 was heated to reflux at 140°C.
• a batch initiator mixture of 1.9g of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 42 and 12.0g of xylene supplied by ExxonMobil, Houston, Texas from means 44 were added all at once to reactor 32.
• another batch initiator mixture of 17.5g of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina,
• the resulting copolymer @ 65.6 weight percent solids had a GPC Mn of 1935 and GPC Mw of 2656 using a polystyrene standard.
• the Tg of the copolymer was 38.6°C, using dynamic scanning calorimetry.
• Copolymer 6 To 1 -liter hybrid reactor 10 fitted with heating jacket 16, stirrer 20, feed lines from means 22 for conveying hybrid reactor monomers, means 24 for conveying hybrid reactor initiator, and means 26 for conveying polymerization medium, an initial polymerization medium charge of 268.4g of xylene supplied by ExxonMobil, Houston, Texas was added from means 26.
• the polymerization medium was heated to 175°C under sub-reflux at 54.7 psia (0.38 MPa) in reactor 10.
• a hybrid monomer mixture of 2489.8g of methyl methacrylate (MMA from Lucite International, Inc., Cordova, Tennessee), 1067.1g of hydroxy ethyl acrylate (Rocryl ® 420 HEA from Rohm and Haas, Philadelphia, Pennsylvania) and 33.3g of xylene supplied by ExxonMobil, Houston, Texas as solvent was added to reactor 10 over a period of 240 minutes in such a way that the level in the reactor 10 was held constant at 0.55 liters and an excess portion of the hybrid reactor contents was fed to an attached 12-liter batch reactor 32 fitted with heating jacket 36, stirrer 38, water cooled condenser with nitrogen purge 46 and a feed line from means 44 for conveying batch reactor initiator.
• a hybrid initiator mixture of 14.5g of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 24 and 803.4g of xylene supplied by ExxonMobil, Houston, Texas from means 26 was added over a period of 240 minutes to reactor 10 under sub-reflux at 54.7 psia (0.38 MPa) in reactor 10. Polymerization temperature of 175°C was maintained in reactor 10 over the entire reaction time. After completion of the feeds to reactor 10, it was drained over 25 minutes into reactor 32. Once transfer from reactor 10 to reactor 32 began, reactor 32 was heated to reflux at 140°C.
• another batch initiator mixture of 17.5g of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 42 and 108.4g of xylene supplied by ExxonMobil, Houston, Texas from means 44 were fed to reactor 32 over 220 minutes.
• the polymerization medium was heated to 175°C under sub-reflux at 65.5 psia (0.45 MPa) in reactor 10.
• MMA methyl methacrylate
• hydroxy ethyl acrylate hydroxy ethyl acrylate
• xylene supplied by ExxonMobil Houston, Texas
• reactor 32 After completion of the feeds to reactor 10, it was drained over 25 minutes into reactor 32. Once transfer from reactor 10 to reactor 32 began, reactor 32 was heated to reflux at 140°C. Thirty-four minutes thereafter, a batch initiator mixture of 1.9g of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 42 and 12. Og of xylene supplied by ExxonMobil, Houston, Texas from means 44 were added all at once to reactor 32. Directly thereafter, another batch initiator mixture of 17.5g of tert-butyl peroxyacetate (Luperox ® 7M75 initiator from Atofina,
• the resulting copolymer @ 64.7 weight percent solids had a GPC Mn of 2683 and GPC Mw of 3386 using a polystyrene standard.
• the Tg of the copolymer was 27.1°C, using dynamic scanning calorimetry.
• Macromonomer 1 To a 1 -liter hybrid reactor 10 fitted with heating jacket 16, stirrer 20, feed lines from means 22 for conveying hybrid reactor monomers, means 24 for conveying hybrid reactor initiator, and means 26 for conveying polymerization medium, an initial polymerization medium charge of 355.
• a hybrid initiator mixture of 27.7g of 2,2'-azobis(2-methyl- butanenitrile) (Vazo ® 67 from DuPont, Bell, West Virginia) from means 24 and 1063.4g of ethyl acetate from means 26 is added over a period of 240 minutes to reactor 10 under sub-reflux at 184.2 psia (1.27 Mpa). Polymerization temperature of 175°C is maintained in reactor 10 over the entire reaction time. After completion of the feeds to reactor 10, it is drained over 25 minutes into reactor 32. Once transfer from reactor 10 to reactor 32 began, reactor 32 is heated to reflux at 77°C.
• Og of ethyl acetate as solvent is added to reactor 10 over a period of 240 minutes in such a way that the level in the reactor 10 is held constant at 0.55 liters and an excess portion of the hybrid reactor contents is fed to an attached 12-liter batch reactor 32 fitted with heating jacket 36, stirrer 38, water cooled condenser with nitrogen purge 46 and a feed line from means 44 for conveying batch reactor initiator. Simultaneously, a hybrid initiator mixture of 26.
• a batch initiator mixture of 1.3g of tert-butyl peroxypivalate (Luperox ® 11 M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 42 and 41.4g of ethyl acetate from means 44 is added all at once to reactor 32.
• another batch initiator mixture of 11.7g of tert-butyl peroxypivalate (Luperox ® 11 M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 42 and 372.2g of ethyl acetate from means 44 is fed to reactor 32 over 235 minutes. Simultaneously, 659.
• n-butyl acrylate (n-butyl acrylate from Rohm and Haas, Philadelphia, Pennsylvania) from means 40 is fed to reactor 32 over 235 minutes.
• still another batch initiator mixture of 12.3g of tert-butyl peroxypivalate (Luperox ® 11 M75 initiator from Atofina, Philadelphia, Pennsylvania) from means 42 and 103.4g of ethyl acetate from means 44 is fed over half an hour to reactor 32.
• the amount of the initiator solution used is 2.0 weight percent based on the total weight of the monomer mixture.
• the reactor 32 is held at reflux for 1 hour and cooled to 80°C.
• the resulting graft copolymer is @ 50.0% solids.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Engineering & Computer Science (AREA)
• Life Sciences & Earth Sciences (AREA)
• General Chemical & Material Sciences (AREA)
• Materials Engineering (AREA)
• Wood Science & Technology (AREA)
• Paints Or Removers (AREA)
• Polymerisation Methods In General (AREA)
• Application Of Or Painting With Fluid Materials (AREA)
• Polyethers (AREA)
• Graft Or Block Polymers (AREA)

Applications Claiming Priority (3)

Publications (2)

Family

ID=33568011

Family Applications (2)

Family Applications Before (1)

Country Status (8)

Families Citing this family (9)

Citations (6)

Family Cites Families (13)

• 2004
  • 2004-07-01 KR KR1020057025289A patent/KR20060038405A/ko not_active Application Discontinuation
  • 2004-07-01 AU AU2004253971A patent/AU2004253971A1/en not_active Abandoned
  • 2004-07-01 WO PCT/US2004/021685 patent/WO2005003243A2/en active Application Filing
  • 2004-07-01 JP JP2006518857A patent/JP2007527451A/ja active Pending
  • 2004-07-01 JP JP2006518858A patent/JP2007523962A/ja active Pending
  • 2004-07-01 MX MXPA05013523A patent/MXPA05013523A/es unknown
  • 2004-07-01 EP EP04756709A patent/EP1639048B1/en not_active Revoked
  • 2004-07-01 BR BRPI0411680-1A patent/BRPI0411680A/pt not_active IP Right Cessation
  • 2004-07-01 MX MXPA05013541A patent/MXPA05013541A/es unknown
  • 2004-07-01 WO PCT/US2004/021684 patent/WO2005003185A1/en active Application Filing
  • 2004-07-01 CA CA002527084A patent/CA2527084A1/en not_active Abandoned
  • 2004-07-01 KR KR1020057025385A patent/KR20060027829A/ko not_active Application Discontinuation
  • 2004-07-01 AU AU2004254267A patent/AU2004254267A1/en not_active Abandoned
  • 2004-07-01 BR BRPI0411635-6A patent/BRPI0411635A/pt not_active Application Discontinuation
  • 2004-07-01 CA CA002526696A patent/CA2526696A1/en not_active Abandoned
  • 2004-07-01 EP EP04777656A patent/EP1639019A4/en not_active Withdrawn

Patent Citations (6)

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events