Patent Application
20200115549
This application claims priority to and the benefit of EP Application No 18200711.2, filed Oct. 16, 2018, the contents of which are incorporated herein by reference in their entirety.
Poly(phenylene ether) is known for its excellent water resistance, dimensional stability, and inherent flame retardancy, as well as high oxygen permeability and oxygen/nitrogen selectivity. Properties such as strength, stiffness, chemical resistance, and heat resistance can be tailored by blending with various other polymers in order to meet the requirements of a wide variety of consumer products, for example, plumbing fixtures, electrical boxes, automotive parts, and insulation for wire and cable.
A commercially relevant poly(phenylene ether) is poly(2,6-dimethyl-1,4-phenylene ether), which is prepared on a large scale by the oxidative polymerization of 2,6-dimethylphenol (also known as 2,6-xylenol). For certain product applications, very high molecular weight poly(2,6 dimethyl-1,4-phenylene ether)s are needed. Not only must the average molecular weight be very high, but the sample should preferably have a small weight percent of low molecular weight polymer chains.
There is therefore a need for poly(phenylene ether)s that have but a high number average molecular weight and a reduced fraction of low molecular weight molecules. There is also a need for improved, commercially scalable, and environmentally acceptable processes for producing such poly(phenylene ether)s.
A method for preparing a poly(phenylene ether) comprises oxidatively polymerizing a poly(phenylene ether) starting material having an initial intrinsic viscosity in the presence of an organic solvent and a copper-amine catalyst to form a reaction mixture comprising a poly(phenylene ether) having a final intrinsic viscosity that is at least 50% greater than the initial intrinsic viscosity; terminating the oxidative polymerization to form a post-termination reaction mixture; combining an aqueous solution comprising a chelant with the post-termination reaction mixture to form a chelation mixture comprising an aqueous phase comprising chelated copper ion, and an organic phase comprising dissolved poly(phenylene ether); separating the aqueous phase and the organic phase; and isolating the poly(phenylene ether) from the organic phase.
A poly(phenylene ether) made by the method and an article comprising the poly(phenylene ether) are also disclosed.
The above described and other features are exemplified by the following detailed description.
The present inventors have advantageously discovered a process effective to produce poly(phenylene ether)s having a high molecular weight and high intrinsic viscosity. Accordingly, an aspect of the present disclosure is a method of preparing a poly(phenylene ether) comprising oxidatively polymerizing a poly(phenylene ether) starting material having an initial intrinsic viscosity in the presence of an organic solvent and a copper-amine catalyst to form a reaction mixture comprising a poly(phenylene ether) having a final intrinsic viscosity that is at least 50% greater than the initial intrinsic viscosity; terminating the oxidative polymerization to form a post-termination reaction mixture; combining an aqueous solution comprising a chelant with the post-termination reaction mixture to form a chelation mixture comprising an aqueous phase comprising chelated copper ion, and an organic phase comprising dissolved poly(phenylene ether); separating the aqueous phase and the organic phase; and isolating the poly(phenylene ether) from the organic phase.
Advantageously, the poly(phenylene ether) starting material comprises a poly(phenylene ether) or a phenylene ether oligomer. The poly(phenylene ether) oligomer can have an intrinsic viscosity of less than 0.2, preferably less than 0.15, more preferably 0.12 or less, more preferably 0.1 or less. Intrinsic viscosity can be determined using an Ubbelohde viscometer at 25° C. in chloroform. The final intrinsic viscosity of the poly(phenylene ether) reaction product is at least 50% greater than the intrinsic viscosity of the phenylene ether oligomer starting material. For example, the final intrinsic viscosity can be greater than 0.20, preferably 0.25 to 0.60, or 0.3 to 0.5, or 0.3 to 0.45.
In some aspects, the poly(phenylene ether) starting material is a poly(phenylene ether) having an intrinsic viscosity of 0.4 to 1.0. The poly(phenylene ether) reaction product can have a final intrinsic viscosity of greater than or equal to 0.80, preferably 0.90 to 1.5.
The poly(phenylene ether) starting material can comprise repeating structural units having the formula
wherein each occurrence of Q1 and Q2 is independently halogen, unsubstituted or substituted C1-12 hydrocarbyl provided that the hydrocarbyl group is not tertiary hydrocarbyl, C1-12 hydrocarbylthio, C1-12 hydrocarbyloxy, or C2-12 halohydrocarbyloxy wherein at least two carbon atoms separate the halogen and oxygen atoms; and each occurrence of Q2 is independently hydrogen, halogen, unsubstituted or substituted C1-12 hydrocarbyl provided that the hydrocarbyl group is not tertiary hydrocarbyl, C1-12 hydrocarbylthio, C1-12 hydrocarbyloxy, or C2-12 halohydrocarbyloxy wherein at least two carbon atoms separate the halogen and oxygen atoms.
In some aspects, the poly(phenylene ether) starting material comprises a homopolymer or copolymer comprising repeating units derived from 2,6-dimethylphenol, 2,3,6-trimethylphenol, and combinations thereof. Preferably, the poly(phenylene ether) starting material comprises at least one phenolic end group per molecule. In some aspects, the poly(phenylene ether) comprises an average of less than 2.0 phenolic end groups. In some aspects, the poly(phenylene ether) comprises an average of 1.8 to less than 2.0 phenolic end groups per molecule.
Preferably, the oxidative polymerization of the poly(phenylene ether) starting material is conducted in the absence of a phenolic monomer. Stated another way, a phenolic monomer is excluded from the reaction mixture. In some aspects, the presence of any phenolic monomers is limited to less than 1000 ppm, or less than 500 ppm, or less than 250 ppm, or less than 100 ppm, or less than 50 ppm, based on the total weight of the poly(phenylene ether) starting material.
The oxidative polymerization is conducted in the presence of an organic solvent. Suitable organic solvents can include alcohols, ketones, aliphatic and aromatic hydrocarbons, chlorohydrocarbons, nitrohydrocarbons, ethers, esters, amides, mixed ether-esters, sulfoxides, and the like, provided they do not interfere with or enter into the oxidation reaction. High molecular weight poly(phenylene ethers) can greatly increase the viscosity of the reaction mixture. Therefore, it is sometimes desirable to use a solvent system that will cause them to precipitate while permitting the lower molecular weight polymers to remain in solution until they form the higher molecular weight polymers. The organic solvent can comprise, for example, toluene, benzene, chlorobenzene, ortho-dichlorobenzene, nitrobenzene, trichloroethylene, ethylene dichloride, dichloromethane, chloroform, or a combination thereof. Preferred solvents include aromatic hydrocarbons. In some aspects, the organic solvent comprises toluene, benzene, chlorobenzene, or a combination thereof, preferably toluene.
The poly(phenylene ether) starting material can be present in the oxidative polymerization reaction mixture in an amount of 3 to 10 weight percent, based on the total weight of the poly(phenylene ether) starting material and the solvent.
The oxidative polymerization is further conducted in the presence of a copper-amine catalyst. The copper source for the copper amine catalyst can comprise a salt of cupric or cuprous ion, including halides, oxides, and carbonates. Alternatively, copper can be provided in the form of a pre-formed salt of an alkylene diamine ligand. Preferred copper salts include cuprous halides, cupric halides, and their combinations. Especially preferred are cuprous bromides, cupric bromides, and combinations thereof.
A preferred copper-amine catalyst comprises a secondary alkylene diamine ligand. Suitable secondary alkylene diamine ligands are described in U.S. Pat. No. 4,028,341 to Hay and are represented by the formula
Rb—NH—Ra—NH—Rc
wherein Ra is a substituted or unsubstituted divalent residue wherein two or three aliphatic carbon atoms form the closest link between the two diamine nitrogen atoms; and Rb and Rc are each independently isopropyl or a substituted or unsubstituted C4-8 tertiary alkyl group. Examples of Ra include ethylene, 1,2-propylene, 1,3-propylene, 1,2-butylene, 1,3-butylene, 2,3-butylene, the various pentylene isomers having from two to three carbon atoms separating the two free valances, phenylethylene, tolylethylene, 2-phenyl-1,2-propylene, cyclohexylethylene, 1,2-cyclohexylene, 1,3-cyclohexylene, 1,2-cyclopropylene, 1,2-cyclobutylene, 1,2-cyclopentylene, and the like. Preferably, Ra is ethylene. Examples of Rb and Rc can include isopropyl, t-butyl, 2-methyl-but-2-yl, 2-methyl-pent-2-yl, 3-methyl-pent-3-yl, 2,3-dimethyl-buty-2-yl, 2,3-dimethylpent-2-yl, 2,4-dimethyl-pent-2-yl, 1-methylcyclopentyl, 1-methylcyclohexyl and the like. A highly preferred example of Rb and Rc is t-butyl. An exemplary secondary alkylene diamine ligand is N,N′-di-t-butylethylenediamine (DBEDA). Suitable molar ratios of copper to secondary alkylene diamine are from 1:1 to 1:5, preferably 1:1 to 1:3, more preferably 1:1.5 to 1:2.
The preferred copper-amine catalyst comprising a secondary alkylene diamine ligand can further comprise a secondary monoamine. Suitable secondary monoamine ligands are described in commonly assigned U.S. Pat. No. 4,092,294 to Bennett et al. and represented by the formula
Rd—NH—Re
wherein Rd and Re are each independently substituted or unsubstituted C1-12 alkyl groups, and preferably substituted or unsubstituted C3-6 alkyl groups. Examples of the secondary monoamine include di-n-propylamine, di-isopropylamine, di-n-butylamine, di-sec-butylamine, di-t-butylamine, N-isopropyl-t-butylamine, N-sec-butyl-t-butylamine, di-n-pentylamine, bis(1,1-dimethylpropyl)amine, and the like. A highly preferred secondary monoamine is di-n-butylamine (DBA). A suitable molar ratio of copper to secondary monoamine is from 1:1 to 1:10, preferably 1:3 to 1:8, and more preferably 1:4 to 1:7.
The preferred copper-amine catalyst comprising a secondary alkylene diamine ligand can further comprise a tertiary monoamine. Suitable tertiary monoamine ligands are described in the abovementioned Hay U.S. Pat. No. 4,028,341 and Bennett U.S. Pat. No. 4,092,294 patents and include heterocyclic amines and certain trialkyl amines characterized by having the amine nitrogen attached to at least two groups which have a small cross-sectional area. In the case of trialkylamines, it is preferred that at least two of the alkyl groups be methyl with the third being a primary C1-8 alkyl group or a secondary C3-8 alkyl group. It is especially preferred that the third substituent have no more than four carbon atoms. A highly preferred tertiary amine is dimethylbutylamine (DMBA). A suitable molar ratio of copper to tertiary amine is less than 1:20, preferably less than 1:15, preferably 1:1 to less than 1:15, more preferably 1:1 to 1:12.
A suitable molar ratio of copper-amine catalyst (measured as moles of metal) to poly(phenylene ether) oligomer starting material is 1:50 to 1:400, preferably 1:100 to 1:200, more preferably 1:100 to 1:180.
The reaction conducted in the presence of a copper-amine catalyst can optionally be conducted in the presence of bromide ion. It has already been mentioned that bromide ion can be supplied as a cuprous bromide or cupric bromide salt. Bromide ion can also be supplied by addition of a 4-bromophenol, such as 2,6-dimethyl-4-bromophenol. Additional bromide ion can be supplied in the form of hydrobromic acid, an alkali metal bromide, or an alkaline earth metal bromide. Sodium bromide and hydrobromic acid are highly preferred bromide sources. A suitable ratio of bromide ion to copper ion is 2 to 20, preferably 3 to 20, more preferably 4 to 7.
In some aspects, each of the above described components of the copper-amine catalyst are added to the oxidative polymerization reaction at the same time.
The oxidative polymerization can optionally further be conducted in the presence of one or more additional components, including a lower alkanol or glycol, a small amount of water, or a phase transfer agent. It is generally not necessary to remove reaction byproduct water during the course of the reaction. In some aspects, a phase transfer agent is present. Suitable phase transfer agents can include, for example, a quaternary ammonium compound, a quaternary phosphonium compound, a tertiary sulfonium compound, or a combination thereof. Preferably, the phase transfer agent can be of the formula (R3)4QX, wherein each R3 is the same or different, and is a C1-10 alkyl; Q is a nitrogen or phosphorus atom; and X is a halogen atom or a C1-8 alkoxy or C6-18 aryloxy. Exemplary phase transfer catalysts include (CH3(CH2)3)4NX, (CH3(CH2)3)4PX, (CH3(CH2)5)4NX, (CH3(CH2)6)4NX, (CH3(CH2)4)4NX, CH3(CH3(CH2)3)3NX, and CH3(CH3(CH2)2)3NX, wherein X is Cl−, Br−, a C1-8 alkoxy or a C6-18 aryloxy. An effective amount of a phase transfer agent can be 0.1 to 10 wt %, or 0.5 to 2 wt %, each based on the weight of the reaction mixture. In a specific aspect, a phase transfer agent is present and comprises N,N,N′N′-didecyldimethyl ammonium chloride.
The oxidative polymerization can be conducted at a temperature of 20 to 70° C., preferably 30 to 60° C., more preferably 45 to 55° C. Depending on the precise reaction conditions chosen, the total polymerization reaction time—that is, the time elapsed between initiating oxidative polymerization and terminating oxidative polymerization—can vary, but it is typically 120 to 250 minutes, specifically 145 to 210 minutes.
The method further comprises terminating the oxidative polymerization to form a post-termination reaction mixture. The reaction is terminated when the flow of oxygen to the reaction vessel is stopped. Residual oxygen in the reaction vessel headspace is removed by flushing with an oxygen-free gas, such as nitrogen.
After the polymerization reaction is terminated, the copper ion of the polymerization catalyst is separated from the reaction mixture. This is accomplished by combining a chelant with the post-termination reaction mixture to form a chelation mixture. The chelant comprises an alkali metal salt of an aminopolycarboxylic acid, preferably an alkali metal salt of an aminoacetic acid, more preferably an alkali metal salt of nitrilotriacetic acid, ethylene diamine tetraacetic acid, or a combination thereof, even more preferably a sodium salt of nitrilotriacetic, a sodium salt of ethylene diamine tetraacetic acid, or a combination thereof. In a specific aspect, the chelant comprises an alkali metal salt of nitrilotriacetic acid. In some aspects, the chelant is a sodium or potassium salt of nitrilotriacetic acid, specifically trisodium nitrilotriacetate. After agitation of the chelation mixture, that mixture comprises an aqueous phase comprising chelated copper ion and an organic phase comprising the dissolved poly(phenylene ether). The chelation mixture can exclude the dihydric phenol required by U.S. Pat. No. 4,110,311 to Cooper et al., the aromatic amine required by U.S. Pat. No. 4,116,939 to Cooper et al., and the mild reducing agents of U.S. Pat. No. 4,110,311 to Cooper et al., which include sulfur dioxide, sulfurous acid, sodium bisulfite, sodium thionite, tin(II) chloride, iron (II) sulfate, chromium (II) sulfate, titanium (III) chloride, hydroxylamines, and salts thereof, phosphates, glucose, and mixtures thereof. The chelation mixture is maintained at a temperature of 40 to 55° C., specifically 45 to 50° C., for 5 to 100 minutes, specifically 10 to 60 minutes, more specifically 15 to 30 minutes. This combination of temperature and time is effective for copper sequestration while also minimizing molecular weight degradation of the poly(phenylene ether). The chelation step includes (and concludes with) separating the aqueous phase and the organic phase of the chelation mixture. This separation step is conducted at a temperature of 40 to 55° C., specifically 45 to 50° C. The time interval of 5 to 100 minutes for maintaining the chelation mixture at 40-55° C. is measured from the time at which the post-termination reaction mixture is first combined with chelant to the time at which separation of the aqueous and organic phases is complete.
The method further comprises isolating the poly(phenylene ether) from the organic phase. Isolation can be by, for example, precipitation of the poly(phenylene ether) which can be induced by appropriate selection of reaction solvent described above, or by the addition of an anti-solvent to the reaction mixture. Suitable anti-solvents include lower alkanols having one to about ten carbon atoms, acetone, and hexane. The preferred anti-solvent is methanol. The anti-solvent can be employed at a range of concentrations relative to the organic solvent, with the optimum concentration depending on the identities of the organic solvent and anti-solvent, as well as the concentration and intrinsic viscosity of the poly(phenylene ether) product. It has been discovered that when the organic solvent is toluene and the anti-solvent is methanol, a toluene:methanol weight ratio of 50:50 to 80:20 is suitable, with ratios of 60:40 to 70:30 being preferred, and 63:37 to 67:33 being more preferred. These preferred and more preferred ratios are useful for producing a desirable powder morphology for the isolated poly(phenylene ether) resin, without generating either stringy powder or excessive powder fines.
The method can optionally comprise pre-concentrating the reaction mixture prior to addition of the anti-solvent. Although it is not possible to pre-concentrate to as great a degree as for lower intrinsic viscosity poly(phenylene ether)s, pre-concentrations of, for example, 15 weight percent poly(phenylene ether) are possible. Any suitable method for pre-concentration can be employed. For example, the preconcentration can be carried out by preheating the solution above its atmospheric boiling point at a pressure modestly elevated above one atmosphere (so that no boiling takes place in the heat exchanger) followed by flashing the solution to a lower pressure and temperature, whereby vaporization of a substantial part of the toluene takes place and the required heat of vaporization is supplied by the heat transferred in the heat exchanger as sensible heat of the solution.
An important advantage of the method described herein is that it produces an isolated poly(phenylene ether) having a number average molecular weight of at least 15,000 grams per mole, or at least 18.00 grams per mole. In some aspects, the number average molecular weight is 18,000 to 100,000 grams per mole, or 18,000 to 60,000 grams per mole, or 30,000 to 60,000 grams per mole. In some aspects, the isolated poly(phenylene ether) can have a weight average molecular weight of at least 75,000 grams per mole, or at least 100,000 grams per mole, or 75,000 to 400,000 grams per mole, or 75,000 to 200,000 grams per mole. Number and weight average molecular weight can be determined by gel permeation chromatography in chloroform relative to polystyrene standards, as described in the working examples below.
A poly(phenylene ether) prepared according to the above described method represents another aspect of the present disclosure. The poly(phenylene ether) can comprise repeating structural units having the formula
wherein Q1 and Q2 are as defined above. The hydrocarbyl residue can also contain one or more carbonyl groups, amino groups, hydroxyl groups, or the like, or it can contain heteroatoms within the backbone of the hydrocarbyl residue. As one example, Q1 can be a di-n-butylaminomethyl group formed by reaction of a terminal 3,5-dimethyl-1,4-phenyl group with the di-n-butylamine component of an oxidative polymerization catalyst.
The poly(phenylene ether) can comprise molecules having aminoalkyl-containing end group(s), typically located in a position ortho to the hydroxy group. Also frequently present are tetramethyldiphenoquinone (TMDQ) end groups, typically obtained from 2,6-dimethylphenol-containing reaction mixtures in which tetramethyldiphenoquinone by-product is present. In some aspects, the poly(phenylene ether) is substantially free of the quinone end groups. For example, the poly(phenylene ether) can include less than 1% of quinone end groups. The poly(phenylene ether) can be in the form of a homopolymer, a copolymer, a graft copolymer, an ionomer, or a block copolymer, as well as combinations thereof.
In a specific aspects, the poly(phenylene ether) is a poly(2,6-dimethyl-1,4-phenylene ether).
Compositions and articles comprising the poly(phenylene ether) made by the above method represent another aspect of the present disclosure. For example, the poly(phenylene ether) made by the method described herein can be useful for forming a thermoplastic composition which can optionally comprises at least one of a thermoplastic polymer different from the poly(phenylene ether) and an additive composition comprising one or more additives. The one or more additives can be selected to achieve a desired property, with the proviso that the additive(s) are also selected so as to not significantly adversely affect a desired property of the thermoplastic composition. The additive composition or individual additives can be mixed at a suitable time during the mixing of the components for forming the composition. The additive can be soluble or non-soluble in poly(phenylene ether). The additive composition can include an impact modifier, flow modifier, filler (e.g., a particulate polytetrafluoroethylene (PTFE), glass, carbon, mineral, or metal), reinforcing agent (e.g., glass fibers), antioxidant, heat stabilizer, light stabilizer, ultraviolet (UV) light stabilizer, UV absorbing additive, plasticizer, lubricant, release agent (such as a mold release agent), antistatic agent, anti-fog agent, antimicrobial agent, colorant (e.g, a dye or pigment), surface effect additive, radiation stabilizer, flame retardant, anti-drip agent (e.g., a PTFE-encapsulated styrene-acrylonitrile copolymer (TSAN)), or a combination thereof. For example, a combination of a heat stabilizer, mold release agent, and ultraviolet light stabilizer can be used. In general, the additives are used in the amounts generally known to be effective. For example, the total amount of the additive composition (other than any impact modifier, filler, or reinforcing agent) can be 0.001 to 10.0 wt %, or 0.01 to 5 wt %, each based on the total weight of the polymer in the composition.
The poly(phenylene ether) or a composition comprising the poly(phenylene ether) can be formed into articles by shaping, extruding, or molding. Articles can be molded from the composition by methods including, for example, injection molding, injection compression molding, gas assist injection molding, rotary molding, blow molding, compression molding, and the like. In some aspects, articles can be formed by injection molding.
This disclosure is further illustrated by the following examples, which are non-limiting.
Materials used for the following examples are provided in Table 1.
Tests were conducted using a laboratory scale jacketed glass reactor with a bottom drain valve, an overhead agitator, a condenser, a dip tube for oxygen bubbling, and thermocouples. Nitrogen was present overhead.
The chemical structure and composition of the oligomers were determined by proton nuclear magnetic resonance (1H NMR) analysis. All 1H NMR spectra were acquired on a Varian Mercury Plus 400 instrument operating at an observe frequency of 400.14 MHz.
Intrinsic viscosity (IV) of the oligomers was examined using an Ubbelohde capillary type viscometer and stop watch. Different concentrations of oligomers were prepared in chloroform and measurements were done at 25° C. in a thermostatted water bath. The flow time data was used to calculate the intrinsic viscosity by extrapolating the reduced viscosity to zero concentration.
Weight average molecular weights were determined by gel permeation chromatography (GPC) in chloroform relative to polystyrene standards.
A bubbling polymerization reactor was loaded with 318.06 grams of toluene, 23.94 grams PPE-1, 0.2394 grams DBA, 3.1806 grams DMBA, 1.2607 grams of a diamine mixture of 30 wt % DBEDA, 7.5 wt % DDAC and the balance toluene, and the contents were stirred under nitrogen atmosphere. A mixture of 1.7671 grams HBr and 0.1402 grams Cu2O was added. The temperature was ramped to 35° C. and oxygen flow was started to the reactor. The temperature was raised to 48° C. at 30 minutes and oxygen flow was maintained for 120 minutes, at which point the oxygen flow was stopped and the bubbling reactor contents were immediately transferred to a vessel containing 5.0376 grams NTA (20%) and 13.0699 g water. The solution was stirred at 60° C. for 2 hours and then it was left to decant. The decanted light phase was precipitated in methanol, filtered, reslurried in methanol and filtered again. The final dry powder was obtained after drying in a vacuum oven at 110° C. Results are shown in Table 2.
A bubbling polymerization reactor was loaded with 237.5 grams of toluene, 12.5 grams PPE-2, 0.1645 grams DBA, 2.3703 grams DMBA, 0.089 grams of a diamine mixture of 30 wt % DBEDA, 7.5 wt % DDAC and the balance toluene, and the contents were stirred under nitrogen atmosphere. A mixture of 0.134 grams HBr and 0.0112 grams Cu2O was added. The temperature was ramped to 35° C. and oxygen flow was started to the reactor. The temperature was raised to 48° C. at 30 minutes. The same amount of HBr and Cu2O was added at 45 minutes and 100 minutes. Oxygen flow was maintained for 240 minutes, at which point the oxygen flow was stopped and the bubbling reactor contents were immediately transferred to a vessel containing 5.0 grams NTA (20%) and 13.0 grams water. The solution was stirred at 60° C. for 2 hours and then it was left to decant. The decanted light phase was precipitated in methanol, filtered, reslurried in methanol and filtered again. The final dry powder was obtained after drying in a vacuum oven at 110° C. Results are shown in Table 3.
A bubbling polymerization reactor was loaded with 310 grams of toluene, 24 grams PPE-3, 0.24 grams DBA, 3.1881 grams DMBA, 1.2628 grams of a diamine mix consisting of 30 wt % DBEDA, 7.5 wt % DDAC and the balance toluene, and the contents were stirred under nitrogen atmosphere. A mixture of 1.7787 grams HBr and 0.1405 grams Cu2O was added. The temperature was ramped to 35° C. and oxygen flow was started to the reactor. The temperature was raised to 48° C. at 30 minutes and oxygen flow was maintained for 120 minutes, at which point the oxygen flow was stopped and the bubbling reactor contents were immediately transferred to a vessel containing 5.0 grams NTA (20%) and 13.0 grams water. The solution was stirred at 60° C. for 2 hours and then it was left to decant. The decanted light phase was precipitated in methanol, filtered, reslurried in methanol and filtered again. The final dry powder was obtained after drying in a vacuum oven at 110° C. Results are shown in Table 4.
This disclosure further encompasses the following aspects.
Aspect 1: A method for preparing a poly(phenylene ether), the method comprising: oxidatively polymerizing a poly(phenylene ether) starting material having an initial intrinsic viscosity in the presence of an organic solvent and a copper-amine catalyst to form a reaction mixture comprising a poly(phenylene ether) having a final intrinsic viscosity that is at least 50% greater than the initial intrinsic viscosity; terminating the oxidative polymerization to form a post-termination reaction mixture; combining an aqueous solution comprising a chelant with the post-termination reaction mixture to form a chelation mixture comprising an aqueous phase comprising chelated copper ion, and an organic phase comprising dissolved poly(phenylene ether); separating the aqueous phase and the organic phase; and isolating the poly(phenylene ether) from the organic phase.
Aspect 2: The method of aspect 1, wherein the poly(phenylene ether) starting material comprises a poly(phenylene ether) oligomer having an initial intrinsic viscosity of less than 0.2, preferably 0.15 or less, more preferably 0.12 or less, more preferably 0.1 or less and the poly(phenylene ether) has a final intrinsic viscosity of greater than 0.20, preferably 0.25 to 0.60, or 0.3 to 0.5, or 0.3 to 0.45.
Aspect 3: The method of aspect 1, wherein the poly(phenylene ether) starting material comprises a poly(phenylene ether) having an initial intrinsic viscosity of 0.4 to 1.0, and the poly(phenylene ether) has a final intrinsic viscosity of greater than or equal to 0.80, preferably 0.90 to 1.5.
Aspect 4: The method of any one of aspects 1 to 3, wherein the oxidative polymerization is conducted in the absence of a phenolic monomer.
Aspect 5: The method of any one of aspects 1 to 4, wherein the organic solvent comprises toluene, benzene, chlorobenzene, or a combination thereof.
Aspect 6: The method of any of aspects 1 to 5, wherein the copper-amine catalyst comprises a copper ion and a hindered secondary amine, preferably wherein the hindered secondary amine has the formula RbHN—Ra—NHRc, wherein Ra is C2-4 alkylene or C3-7cycloalkylene and Rb and Rc are isopropyl or C4-8 tertiary alkyl wherein only the α-carbon atom has no hydrogens, there being at least two and no more than three carbon atoms separating the two nitrogen atoms, more preferably wherein the hindered secondary amine is di-tert-butylethylenediamine.
Aspect 7: The method of aspect 6, wherein the oxidative polymerization is further in the presence of a secondary monoamine, a tertiary monoamine, or a combination thereof, preferably wherein the secondary monoamine comprises di-n-butylamine and the tertiary monoamine comprises N,N-dimethylbutylamine.
Aspect 8: The method of any of aspects 1 to 7, wherein the oxidative polymerization is further in the presence of a bromide ion.
Aspect 9: The method of any of aspects 1 to 8, wherein the oxidative polymerization is further in the presence of a phase transfer agent, preferably wherein the phase transfer agent comprises a quaternary ammonium compound, a quaternary phosphonium compound, a tertiary sulfonium compound, or a combination thereof, more preferably wherein the phase transfer agent comprises N,N,N′N′-didecyldimethyl ammonium chloride.
Aspect 10: The method of any of aspects 1 to 9, wherein the chelant comprises an alkali metal salt of an aminopolycarboxylic acid, preferably an alkali metal salt of an aminoacetic acid, more preferably an alkali metal salt of nitrilotriacetic acid, ethylene diamine tetraacetic acid, or a combination thereof, even more preferably a sodium salt of nitrilotriacetic, a sodium salt of ethylene diamine tetraacetic acid, or a combination thereof.
Aspect 11: The method of any of aspects 1 to 10, wherein the oxidative polymerization is at a temperature of 20 to 70° C., preferably 30 to 60° C., more preferably 45 to 55° C.
Aspect 12: The method of any of aspects 1 to 11, wherein the poly(phenylene ether) starting material is present in an amount of 3 to 10 weight percent, based on the total weight of the poly(phenylene ether) starting material and the solvent.
Aspect 13: A poly(phenylene ether) made by the method of any of aspects 1 to 12.
Aspect 14: An article comprising the poly(phenylene ether) of aspect 13.
The compositions, methods, and articles can alternatively comprise, consist of, or consist essentially of, any appropriate materials, steps, or components herein disclosed. The compositions, methods, and articles can additionally, or alternatively, be formulated so as to be devoid, or substantially free, of any materials (or species), steps, or components, that are otherwise not necessary to the achievement of the function or objectives of the compositions, methods, and articles.
All ranges disclosed herein are inclusive of the endpoints, and the endpoints are independently combinable with each other. “Combinations” is inclusive of blends, mixtures, alloys, reaction products, and the like. The terms “first,” “second,” and the like, do not denote any order, quantity, or importance, but rather are used to distinguish one element from another. The terms “a” and “an” and “the” do not denote a limitation of quantity, and are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. “Or” means “and/or” unless clearly stated otherwise. Reference throughout the specification to “some aspects,” “an aspect,” and so forth, means that a particular element described in connection with the aspect is included in at least one aspect described herein, and may or may not be present in other aspects. The term “combination thereof” as used herein includes one or more of the listed elements, and is open, allowing the presence of one or more like elements not named. In addition, it is to be understood that the described elements may be combined in any suitable manner in the various aspects.
Unless specified to the contrary herein, all test standards are the most recent standard in effect as of the filing date of this application, or, if priority is claimed, the filing date of the earliest priority application in which the test standard appears.
Unless defined otherwise, technical and scientific terms used herein have the same meaning as is commonly understood by one of skill in the art to which this application belongs. All cited patents, patent applications, and other references are incorporated herein by reference in their entirety. However, if a term in the present application contradicts or conflicts with a term in the incorporated reference, the term from the present application takes precedence over the conflicting term from the incorporated reference.
Compounds are described using standard nomenclature. For example, any position not substituted by any indicated group is understood to have its valency filled by a bond as indicated, or a hydrogen atom. A dash (“-”) that is not between two letters or symbols is used to indicate a point of attachment for a substituent. For example, —CHO is attached through carbon of the carbonyl group.
As used herein, the term “hydrocarbyl,” whether used by itself, or as a prefix, suffix, or fragment of another term, refers to a residue that contains only carbon and hydrogen. The residue can be aliphatic or aromatic, straight-chain, cyclic, bicyclic, branched, saturated, or unsaturated. It can also contain combinations of aliphatic, aromatic, straight chain, cyclic, bicyclic, branched, saturated, and unsaturated hydrocarbon moieties. However, when the hydrocarbyl residue is described as substituted, it may, optionally, contain heteroatoms over and above the carbon and hydrogen members of the substituent residue. Thus, when specifically described as substituted, the hydrocarbyl residue can also contain one or more carbonyl groups, amino groups, hydroxyl groups, or the like, or it can contain heteroatoms within the backbone of the hydrocarbyl residue. The term “alkyl” means a branched or straight chain, unsaturated aliphatic hydrocarbon group, e.g., methyl, ethyl, n-propyl, i-propyl, n-butyl, s-butyl, t-butyl, n-pentyl, s-pentyl, and n- and s-hexyl. “Alkenyl” means a straight or branched chain, monovalent hydrocarbon group having at least one carbon-carbon double bond (e.g., ethenyl (—HC═CH2)). “Alkoxy” means an alkyl group that is linked via an oxygen (i.e., alkyl-O—), for example methoxy, ethoxy, and sec-butyloxy groups. “Alkylene” means a straight or branched chain, saturated, divalent aliphatic hydrocarbon group (e.g., methylene (—CH2—) or, propylene (—(CH2)3—)). “Cycloalkylene” means a divalent cyclic alkylene group, —CnH2n-x, wherein x is the number of hydrogens replaced by cyclization(s). “Cycloalkenyl” means a monovalent group having one or more rings and one or more carbon-carbon double bonds in the ring, wherein all ring members are carbon (e.g., cyclopentyl and cyclohexyl). “Aryl” means an aromatic hydrocarbon group containing the specified number of carbon atoms, such as phenyl, tropone, indanyl, or naphthyl. “Arylene” means a divalent aryl group. “Alkylarylene” means an arylene group substituted with an alkyl group. “Arylalkylene” means an alkylene group substituted with an aryl group (e.g., benzyl). The prefix “halo” means a group or compound including one more of a fluoro, chloro, bromo, or iodo substituent. A combination of different halo groups (e.g., bromo and fluoro), or only chloro groups can be present. The prefix “hetero” means that the compound or group includes at least one ring member that is a heteroatom (e.g., 1, 2, or 3 heteroatom(s)), wherein the heteroatom(s) is each independently N, O, S, Si, or P. “Substituted” means that the compound or group is substituted with at least one (e.g., 1, 2, 3, or 4) substituents that can each independently be a C1-9 alkoxy, a C1-9 haloalkoxy, a nitro (—NO2), a cyano (—CN), a C1-6 alkyl sulfonyl (—S(═O)2-alkyl), a C6-12 aryl sulfonyl (—S(═O)2-aryl), a thiol (—SH), a thiocyano (—SCN), a tosyl (CH3C6H4SO2—), a C3-12 cycloalkyl, a C2-12 alkenyl, a C5-12 cycloalkenyl, a C6-12 aryl, a C7-13 arylalkylene, a C4-12 heterocycloalkyl, and a C3-12 heteroaryl instead of hydrogen, provided that the substituted atom's normal valence is not exceeded. The number of carbon atoms indicated in a group is exclusive of any substituents. For example —CH2CH2CN is a C2 alkyl group substituted with a nitrile.
While particular aspects have been described, alternatives, modifications, variations, improvements, and substantial equivalents that are or may be presently unforeseen may arise to applicants or others skilled in the art. Accordingly, the appended claims as filed and as they may be amended are intended to embrace all such alternatives, modifications variations, improvements, and substantial equivalents.
| Number | Date | Country | Kind |
|---|---|---|---|
| 18200711.2 | Oct 2018 | EP | regional |
