Halogen recovery by K+-containing oxidizing agents in the process of halogenating unsaturated isoolefin copolymers

Abstract

A method for producing a halogenated isoolefin copolymer includes contacting an unsaturated isoolefin copolymer cement, comprising an unsaturated isoolefin copolymer dissolved in an organic solvent, with a halogenating agent and an aqueous solution of a potassium salt-based oxidizing agent under halogenation conditions to form a two-phase reaction medium comprising an organic phase and an aqueous phase, wherein the oxidizing agent is capable of converting hydrogen halide to free halogen. The method provides improved halogen recovery, is less sensitive to the presence of water, and utilizes a more stable and environmentally friendly oxidizing agent.

Description

[Technical field]

[0001] This application relates to a method for halogenating unsaturated isoolefin copolymers. [Background technology]

[0002] In the standard process for brominating butyl rubber to form bromobutyl rubber, molecular bromine (Br2) is used as the brominating agent. This process generates hydrogen bromide (HBr) as a by-product, which does not further brominate the butyl rubber polymer under normal conditions. Thus, the theoretical maximum percentage of bromine present in the reaction mixture that can be introduced into the butyl rubber polymer is 50%. However, in practice, this percentage is usually less than 45% and less than 35% in both laboratory and manufacturing plant environments.

[0003] Known methods for improving bromine utilization during the bromination of butyl rubber (WO 2020 / 124222, US 2014 / 0309362, US 3018275, US 5681901) include the application of at least 0.5 moles of a water-soluble oxidizing agent, such as an organic peracid or hydrogen peroxide, per mole of brominating agent, which reoxidizes the hydrogen bromide back to elemental bromine. The oxidizing agent may be an aqueous solution or an aqueous emulsion in an organic solvent. Because the oxidizing agent is only soluble in water, the rate of the reaction is governed by the rate at which the reactants can shuttle between the organic and aqueous phases, thus requiring longer reaction times.

[0004] Furthermore, methods utilizing hydrogen peroxide require very low concentrations of water to be present in the bromination medium, which presents significant challenges and costs commercially since water concentrations above 1 wt% dramatically reduce the benefits seen from using hydrogen peroxide in the bromination medium and may require additional equipment and energy to reduce the water content in the bromination medium from 10-20 wt% to less than 1 wt%.

[0005] In addition, some processes require post-halogenation recycling by neutralizing HBr to obtain sodium bromide (NaBr), washing the NaBr from the halogenated butyl rubber into an aqueous stream, and converting the NaBr to Br2 using Cl2 gas, for example, via a blow-out process. This ex situ recycling process is limited by the extraction efficiency of NaBr into the aqueous phase and the dilution of NaBr in the aqueous phase. Furthermore, performing such ex situ processes is cost-ineffective and energy intensive. [Prior art documents] [Patent documents]

[0006] [Patent Document 1] International Publication No. 2020 / 124222 [Patent Document 2] US Patent No. 2014 / 0309362 [Patent Document 3] U.S. Patent No. 3,018,275 [Patent Document 4] U.S. Patent No. 5,681,901 [Patent Document 5] U.S. Patent No. 5,886,106 [Non-patent literature]

[0007] [Non-Patent Document 1] Rubber Technology, 3rd ed., Maurice Morton, ed., Kluwer Academic Publishers, pp. 297-300 Summary of the Invention [Problem to be solved by the invention]

[0008] There remains a need for cost-effective and efficient methods to improve halogen utilization, especially in the halogenation of isoolefin copolymers, such as butyl rubber, in the presence of significant amounts of water. [Means for solving the problem]

[0009] In one aspect, a method for producing a halogenated isoolefin copolymer is provided, the method comprising contacting an unsaturated isoolefin copolymer cement comprising an unsaturated isoolefin copolymer dissolved in an organic solvent with a halogenating agent and an aqueous solution of a potassium salt-based oxidizing agent under halogenation conditions to form a two-phase reaction medium comprising an organic phase and an aqueous phase, the oxidizing agent being capable of converting hydrogen halide to free halogen.

[0010] The method may further include recovering the halogenated isoolefin copolymer containing at least 0.05 mol % combined halogen.

[0011] The halogenation method of the present invention advantageously provides improved halogen utilization by oxidizing hydrogen halide (HX) formed in the halogenation of unsaturated isoolefin copolymer back to molecular halogen (X2). The method is less sensitive to the presence of water in the cement, achieves better bromine recovery compared to similar methods (e.g., methods utilizing peracid or hydrogen peroxide) while providing good bromine recovery or using less oxidizing agent, and utilizes an oxidizing agent that is more stable to water and temperature and easier to handle than oxidizing agents previously used in similar methods. The method does not fundamentally affect the microstructure and molecular weight of the resulting halogenated isoolefin copolymer, and the ability to achieve comparable or better halogenation efficiency using less oxidizing agent is further beneficial in maintaining the microstructure and molecular weight of the halogenated isoolefin copolymer.

[0012] Additional features will be described or will become apparent during the course of the following detailed description. It should be understood that each feature described herein may be utilized in any combination with any one or more of the other described features, and that each feature does not necessarily depend on the presence of another feature, unless otherwise apparent to one of ordinary skill in the art.

[0013] For a clearer understanding, preferred embodiments will now be described in detail, by way of example, with reference to the accompanying drawings, in which: [Brief description of the drawings]

[0014] [Figure 1] 1 is a graph of active oxygen (wt%) in potassium peroxymonosulfate samples as a function of time (min) in an aqueous solution of potassium peroxymonosulfate (0.1 g / mL) at 45° C. [Diagram 2] FIG. 1 is a graph of functional group Br (mol%) versus reaction time (min) for the bromination of a butyl rubber cement containing 20 wt. % butyl rubber (IIR) and 5 wt. % added water at 45° C. in the absence of oxidant and phase transfer catalyst (triangles); in the presence of 6.4 g potassium peroxymonosulfate oxidant (diamonds); and in the presence of 6.4 g potassium peroxymonosulfate oxidant with 120 mg Lutensol™ TO5 phase transfer catalyst (squares). [Diagram 3] FIG. 2 is a portion of a 1H NMR spectrum in CDCl3 for brominated butyl rubber produced in CDCl3 in the presence of potassium peroxymonosulfate. [Figure 4A] FIG. 1 is a graph of functional group Br (mol%) versus reaction time (min) for the bromination of a butyl rubber cement containing 20 wt. % butyl rubber (IIR), 6.4 g potassium peroxymonosulfate oxidizer, and 240 mg Lutensol™ TO5 phase transfer catalyst at 45° C. with 5 wt. % water added (diamonds) and 15 wt. % water added (squares). [Figure 4B] FIG. 1 is a graph of bromine atom efficiency (BAE) (%) versus added water concentration (wt%) for the bromination of butyl rubber cement containing 20 wt% butyl rubber (IIR), 3.2 potassium peroxymonosulfate oxidizer, and 240 mg Lutensol™ TO5 phase transfer catalyst at 45° C. Samples were taken after 5 minutes (diamonds) and 60 minutes (squares). [Figure 5A]FIG. 1 is a graph of functional group Br (mol%) versus reaction time (min) for the bromination of butyl rubber cement containing 20 wt. % butyl rubber (IIR), 5 wt. % added water at 45° C. with no oxidant and 240 mg Lutensol™ TO5 phase transfer catalyst (diamonds); with 3.2 g potassium peroxymonosulfate oxidant and 240 mg Lutensol™ TO5 phase transfer catalyst (squares); and with 6.4 g potassium peroxymonosulfate oxidant and 240 mg Lutensol™ TO5 phase transfer catalyst (triangles). [Figure 5B] % butyl rubber (IIR), 10 wt. % added water at 45° C.; [Figure 5C] % butyl rubber (IIR), 15 wt. % added water at 45° C.; with no oxidant and 240 mg Lutensol™ TO5 phase transfer catalyst (squares); with 1.6 g potassium peroxymonosulfate oxidant and 240 mg Lutensol™ TO5 phase transfer catalyst (x); with 3.2 g potassium peroxymonosulfate oxidant and 240 mg Lutensol™ TO5 phase transfer catalyst (diamonds); with 6.4 g potassium peroxymonosulfate oxidant and 240 mg Lutensol™ TO5 phase transfer catalyst (triangles). [Figure 6] FIG. 1 is a graph of BAE vs. butyl rubber (IIR) concentration (wt%) for the bromination of butyl rubber cement containing 20 wt.% butyl rubber (IIR), 10-25 wt.% added water at 45° C. at 5 minutes (circles) and 60 minutes (x) using 3.2 g potassium peroxymonosulfate oxidant and 240 mg Lutensol™ TO5 phase transfer catalyst. [Figure 7] 1 is a graph of functional group Br (mol%) versus reaction time (min) for the bromination of a butyl rubber cement containing 20 wt% butyl rubber (IIR) and 5 wt% added water, 6.4 g potassium peroxymonosulfate oxidant and 120 mg Lutensol™ TO5 phase transfer catalyst at 45° C. (diamonds) compared to a control bromination without oxidant (triangles), showing the effect of adding the oxidant as a solid to the cement after the water and phase transfer catalyst have been added but before bromination has begun. [Figure 8] FIG. 1 is a graph of functional group Br (mol%) versus reaction time (min) for the bromination of butyl rubber cement containing 20 wt. % butyl rubber (IIR), 10 wt. % added water, 3.2 g potassium peroxymonosulfate oxidant, and 240 mg Lutensol™ TO5 phase transfer catalyst for processes conducted at 23° C. (squares), 35° C. (triangles), and 45° C. (diamonds). [Figure 9] % butyl rubber (IIR), 5 wt. % added water at 45° C. in the presence of 1.74 g potassium bromate (triangles) and in the presence of 1.74 g potassium bromate and 240 mg Lutensol™ TO5 (circles). [Figure 10]% butyl rubber (IIR), 10 wt. % added water at 45° C. in the presence of 6.5 mL sodium hypochlorite (squares) and in the presence of 6.5 mL sodium hypochlorite and 240 mg Lutensol™ TO5 (x). DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0015] The process involves polymerizing at least one isoolefin monomer and at least one copolymerizable unsaturated monomer in an organic diluent to produce a halogenatable isoolefin copolymer in an organic medium. The polymerization is carried out in a polymerization reactor. Suitable polymerization reactors include flow-through polymerization reactors, plug flow reactors, moving belt or drum reactors, and the like. The process preferably involves a slurry polymerization of the monomers.

[0016] The halogenatable isoolefin copolymer preferably comprises repeat units derived from at least one isoolefin monomer and at least one copolymerizable unsaturated monomer, and optionally repeat units derived from one or more further copolymerizable monomers. The halogenatable isoolefin copolymer preferably comprises an unsaturated isoolefin copolymer.

[0017] Suitable isoolefin monomers include hydrocarbon monomers having 4 to 16 carbon atoms. In one embodiment, the isoolefin monomer has 4 to 7 carbon atoms. Examples of suitable isoolefins include isobutene (isobutylene), 2-methyl-1-butene, 3-methyl-1-butene, 2-methyl-2-butene, 4-methyl-1-pentene, 4-methyl-1-pentene, and mixtures thereof. A preferred isoolefin monomer is isobutene (isobutylene).

[0018] Suitable copolymerizable unsaturated monomers include multiolefins, p-methylstyrene, β-pinene, or mixtures thereof. Multiolefin monomers include hydrocarbon monomers having 4 to 14 carbon atoms. In some embodiments, the multiolefin monomer is a conjugated diene. Examples of suitable conjugated diene monomers include isoprene, butadiene, 2-methylbutadiene, 2,4-dimethylbutadiene, piperylene, 3-methyl-1,3-pentadiene, 2,4-hexadiene, 2-neopentylbutadiene, 2-methyl-1,5-hexadiene, 2,5-dimethyl-2,4-hexadiene, 2-methyl-1,4-pentadiene, 4-butyl-1,3-pentadiene, 2,3-dimethyl-1,3-pentadiene, 2,3-dibutyl-1,3-pentadiene, 2-ethyl-1,3-pentadiene, 2-ethyl-1,3-butadiene, 2-methyl-1,6-heptadiene, cyclopentadiene, methylcyclopentadiene, cyclohexadiene, 1-vinyl-cyclohexadiene, and mixtures thereof.

[0019] The halogenatable isoolefin copolymer may optionally include one or more additional copolymerizable monomers. Suitable additional copolymerizable monomers include, for example, styrenic monomers such as alkyl-substituted vinyl aromatic comonomers, including, but not limited to, C1-C4 alkyl-substituted styrenes. Specific examples of additional copolymerizable monomers include, for example, α-methylstyrene, p-methylstyrene, chlorostyrene, cyclopentadiene, and methylcyclopentadiene. Indene and other styrene derivatives may also be used. In one embodiment, the halogenatable isoolefin copolymer may include a random copolymer of isobutylene, isoprene, and p-methylstyrene.

[0020] In one embodiment, the halogenatable isoolefin copolymer may be formed by copolymerization of a monomer mixture. Preferably, the monomer mixture comprises about 80-99.9 mol% of at least one isoolefin monomer and about 0.1-20 mol% of at least one copolymerizable unsaturated monomer, based on the monomers in the monomer mixture. More preferably, the monomer mixture comprises about 90-99.9 mol% of at least one isoolefin monomer and about 0.1-10 mol% of at least one copolymerizable unsaturated monomer. In one embodiment, the monomer mixture comprises about 92.5-97.5 mol% of at least one isoolefin monomer and about 2.5-7.5 mol% of at least one copolymerizable unsaturated monomer. In another embodiment, the monomer mixture comprises about 97.4-95 mol% of at least one isoolefin monomer and about 2.6-5 mol% of at least one copolymerizable unsaturated monomer.

[0021] When the monomer mixture comprises a further copolymerizable monomer together with the isoolefin and / or the copolymerizable unsaturated monomer, the further copolymerizable monomer preferably replaces a portion of the copolymerizable unsaturated monomer. When a multiolefin monomer is used, the monomer mixture may also comprise 0.01% to 1% by weight of at least one multiolefin crosslinking agent, and when the multiolefin crosslinking agent is present, the amount of the multiolefin monomer is reduced accordingly.

[0022] The unsaturated isoolefin copolymer may be prepared by any suitable method, some of which are known in the art. For example, the polymerization of the monomers may be carried out in a diluent in the presence of an initiator system (e.g., a Lewis acid catalyst and a proton source) capable of initiating the polymerization process. Proton sources suitable in the present invention include any compound that will generate protons when added to a Lewis acid or a composition containing a Lewis acid. Protons can result from the reaction of a Lewis acid with a proton source to generate protons and corresponding by-products. Such reactions may be preferred in the event that the reaction of the proton source with the protonated additive is faster compared to its reaction with the monomer. Proton-generating reactants include, for example, water, alcohols, phenols, thiols, carboxylic acids, and the like, or any mixture thereof. Water, alcohols, phenols, or any mixture thereof are preferred. The most preferred proton source is water. The preferred ratio of Lewis acid to proton source is 5:1 to 100:1 by weight, or 5:1 to 50:1 by weight. The initiator system, including the catalyst and the proton source, is preferably present in the reaction mixture in an amount of 0.02 to 0.1 wt %, based on the total weight of the reaction mixture.

[0023] Alkyl aluminum halide catalysts are a particularly preferred class of Lewis acids for catalyzing the solution polymerization reaction according to the present invention. Examples of alkyl aluminum halide catalysts include methyl aluminum dibromide, methyl aluminum dichloride, ethyl aluminum dibromide, ethyl aluminum dichloride, butyl aluminum dibromide, butyl aluminum dichloride, dimethyl aluminum bromide, dimethyl aluminum chloride, diethyl aluminum bromide, diethyl aluminum chloride, dibutyl aluminum bromide, dibutyl aluminum chloride, methyl aluminum sesquibromide, methyl aluminum sesquichloride, ethyl aluminum sesquibromide, ethyl aluminum sesquichloride, and any mixtures thereof. Preferred are diethyl aluminum chloride (EtAlCl or DEAC), ethyl aluminum sesquichloride (Et 1.5AlCl 1.5 or EASC), ethylaluminum dichloride (EtAlCl2 or EADC), diethylaluminum bromide (Et2AlBr or DEAB), ethylaluminum sesquibromide (Et 1.5 AlBr 1.5 or EASB), and ethylaluminum dibromide (EtAlBr2 or EADB), and any mixtures thereof. In a particularly preferred initiator system, the catalyst comprises ethylaluminum sesquichloride, preferably produced by mixing equimolar amounts of diethylaluminum chloride and ethylaluminum dichloride, preferably in a diluent. The diluent is preferably the same as that used to carry out the copolymerization reaction.

[0024] The diluent may include an organic diluent. Suitable organic diluents may include, for example, alkanes, chloroalkanes, cycloalkanes, aromatics, hydrofluorocarbons (HFCs), or any mixture thereof. Chloroalkanes may include, for example, methyl chloride, dichloromethane, or a mixture thereof. Methyl chloride is particularly preferred. Alkanes and cycloalkanes may include, for example, isopentane, cyclopentane, 2,2-dimethylbutane, 2,3-dimethylbutane, 2-methylpentane, 3-methylpentane, n-hexane, methylcyclopentane, 2,2-dimethylpentane, or any mixture thereof. The alkanes and cycloalkanes are preferably C6 solvents, including n-hexane, or hexane isomers, such as 2-methylpentane or 3-methylpentane, or mixtures of n-hexane and such isomers, and cyclohexane. The monomers are generally cationic polymerized in the diluent at temperatures ranging from −120° C. to +20° C., preferably from −100° C. to −50° C., more preferably from −95° C. to −65° C. The temperature is preferably about −80° C. or less.

[0025] In the case where the diluent comprises a cycloalkane (e.g., methyl chloride) in a slurry polymerization process, the diluent and any residual monomers can be removed from the unsaturated isoolefin copolymer by flash separation using steam. Removal of the diluent and residual monomers in such a "wet" process leaves the polymer containing a large amount of water. The polymer is dissolved in an organic solvent to obtain a polymer cement having a large amount of water content, for example, 1 wt% or more, or 1.5 wt% or more, based on the total weight of the cement. In some embodiments, the water content of the cement can be 0-30 wt%, or 0-25 wt%, or 1-30 wt%, or 1.5-15 wt%, or 2-30 wt%, or 2-20 wt%, or 2-15 wt%, or 5-20 wt%, or 5-15 wt%, or 5-10 wt%, or 10-15 wt%, based on the total weight of the cement.

[0026] In the case of a slurry or solution polymerization process, where the diluent comprises a chloroalkane (e.g., methyl chloride) or an alkane (e.g., hexane), the diluent and any residual monomers can be removed from the unsaturated isoolefin copolymer by flash separation using a heated organic solvent in which the unsaturated isoolefin copolymer is soluble, or by simple distillation. When simple distillation is used, a portion of the organic diluent may remain as an organic solvent in the cement. Removal of the diluent and residual monomers in such a "dry" process results in a polymer cement containing less water, for example less than 1 wt. % or even 0 wt. % water based on the total weight of the cement.

[0027] To form the halogenated isoolefin copolymer, the unsaturated isoolefin copolymer may be subjected to a halogenation process using a halogenating agent under halogenation conditions.Halogenation can be carried out by modifying processes known to those skilled in the art (e.g., the procedures described in Rubber Technology, 3rd Edition, edited by Maurice Morton, Kluwer Academic Publishers, pp. 297-300, or U.S. Patent No. 5,886,106, issued March 23, 1999, the contents of both of which are incorporated herein by reference) and modifying the process as described herein.

[0028] To improve the efficiency of the halogenation, the halogenation process is modified by contacting the unsaturated isoolefin copolymer cement dissolved in an organic solvent with a halogenating agent and an aqueous solution of a potassium salt-based oxidizing agent. A two-phase reaction medium is formed, including an organic phase and an aqueous phase. The oxidizing agent in-situ oxidizes the halides produced in the halogenation process back to molecular halogens, improving the halogen atom efficiency of the halogenation process.

[0029] Halogenating agents useful for halogenating the unsaturated isoolefin copolymer may include molecular chlorine (Cl2) or molecular bromine (Br2), and / or organic or inorganic halide precursors, such as dibromodimethylhydantoin, trichloroisocyanuric acid (TCIA), n-bromosuccinimide, sodium bromide, hydrogen bromide, and the like. Preferably, the halogenating agent includes chlorine (Cl2) or bromine (Br2), more preferably bromine. Preferably, the halogenation includes bromination. The amount of halogenating agent added is controlled to achieve a final halogen content of at least 0.05 mol%, preferably 0.05-2.5 mol% in the halogenated isoolefin copolymer. The amount of halogenating agent used has a linear relationship with the final halogen content (i.e., the amount of functional halogen) on the halogenated isoolefin copolymer. A larger amount of halogenating agent results in a larger amount of functional halogen in the halogenated isoolefin copolymer.

[0030] The halogenation is carried out in a reaction medium comprising an organic solvent, preferably an aliphatic solvent, preferably an alkane, more preferably hexane or pentane.

[0031] The halogenation can be carried out for a length of time that achieves the desired level of halogenation. The length of time is preferably 60 minutes or less. Significant halogenation of the unsaturated isoolefin copolymer can be achieved in 20 minutes or less, or 10 minutes or less, or even 5 minutes or less. Preferably, the halogenation is carried out in as little as 1 minute. Preferably, the halogenation time is from 1 to 60 minutes, or from 1 to 20 minutes, or from 1 to 10 minutes, or from 1 to 5 minutes.

[0032] The halogenation can be carried out at any suitable temperature, preferably up to about 90°C. In some embodiments, the temperature may be up to about 80°C. In other embodiments, the temperature may be up to about 65°C. The increased halogenation efficiency at low temperatures is more pronounced at higher concentrations of unsaturated isoolefin copolymer in the reaction medium. Temperatures in the range of 0-70°C, or 0-50°C, or 0-45°C, or 15-45°C, or 20-45°C, or 40-45°C, or 30-70°C, or 20-60°C, or 23-54°C, or 23-45°C, or 10-35°C, or 20-30°C are preferred. In one embodiment, the unsaturated isoolefin copolymer is cooled before contacting the solution of the unsaturated isoolefin copolymer cement with an aqueous solution of a halogenating agent and an oxidizing agent.

[0033] The unsaturated isoolefin copolymer is preferably present in the reaction medium in an amount of 1 to 60 wt%, based on the total weight of the reaction medium. More preferably, the unsaturated isoolefin copolymer is present in an amount of 5 to 50 wt%, even more preferably 5 to 40 wt%, still more preferably 10 to 33 wt%, even more preferably 10 to 30 wt%, for example 20 wt%, based on the total weight of the reaction medium.

[0034] The aqueous phase is formed from an aqueous solution of the oxidizing agent, water from the halogenation reaction, and additional water contained in the unsaturated isoolefin polymer cement. The aqueous solution of the oxidizing agent together with the water from the halogenation reaction typically constitutes less than 1 wt. % of the reaction medium, for example 0.03 to 0.3 wt. %, based on the total weight of the reaction medium.

[0035] The reaction medium may contain 0-20 wt% additional water based on the total weight of the reaction medium, which is attributable to the water contained in the unsaturated isoolefin polymer cement depending on the process used to prepare the polymer cement. The additional water is water derived from the unsaturated isoolefin polymer cement and does not include water used to prepare the aqueous solution of the oxidizing agent or water resulting from the halogenation reaction. An advantage of the method of the present invention is that the reaction medium may contain a significant amount of additional water, for example, 1-20 wt% additional water based on the total weight of the reaction medium. In some embodiments, the additional water may constitute 1.5-15 wt%, or 2-20 wt%, or 2-15 wt%, or 5-20 wt%, or 5-15 wt%, or 5-10 wt% of the reaction medium based on the total weight of the reaction medium. Even so, in some embodiments, the reaction medium may contain a small amount of additional water, for example, less than 1 wt% additional water based on the total weight of the reaction medium, or even 0 wt% additional water.

[0036] The potassium salt-based oxidizer preferably comprises a salt of potassium cation and one or more peroxy anions, which have the ability to act as an oxidizer for halide ions (e.g., chloride or bromide ions, especially bromide ions). Although mixed salts with one or more other cations (e.g., sodium, lithium, etc.) can be used, salts with only potassium cations are preferred. In some embodiments, the potassium salt-based oxidizer comprises KHSO5, K2S2O8, KClO, KBrO, KBrO3, KIO3, KClO3, KClO4, KIO4, compounds that produce the above potassium salt-based oxidizers, or mixtures thereof. Preferably, the potassium salt-based oxidizer comprises KHSO5, or compounds that produce KHSO5. Potassium peroxymonosulfate is particularly preferred. Potassium peroxymonosulfate produces KHSO5 as an effective oxidizer species.

[0037] Potassium peroxymonosulfate (KHSO5·0.5KHSO4·0.5K2SO4) is a commercially available water-soluble potassium triple salt. Potassium peroxymonosulfate is a white, crystalline, stable solid that is easy to handle, non-toxic, odorless, stable, and inexpensive. Aqueous solutions of potassium peroxymonosulfate have a pH of 2 and are stable at 45°C for at least 1 hour, but decompose when the pH exceeds 3. Potassium peroxymonosulfate produces only KHSO4 as an oxidation by-product. Table 1 compares the properties of potassium peroxymonosulfate with other known oxidizing agents. The standard oxidation potential of potassium peroxymonosulfate is 1.85 V, which is close to that of H2O2 and peracetic acid, indicating that potassium peroxymonosulfate can oxidize halides to halogens. Potassium peroxymonosulfate has a higher temperature of decomposition compared to H2O2 and peracetic acid, which allows for easier storage and transportation and a longer shelf life. Potassium peroxymonosulfate is a solid, which allows for easier handling and maintenance of the desired stoichiometry. Potassium peroxymonosulfate produces its only by-product, KHSO4, which is easily washed away in the neutralization process. Potassium peroxymonosulfate is odorless and therefore will not impart any odor to the finished product.

[0038] [Table 1]

[0039] A phase transfer catalyst is preferably used since the potassium salt-based oxidizing agent is substantially insoluble in organic solvents. The phase transfer catalyst preferably complexes potassium ions to facilitate the transfer of the oxidizing agent into the organic phase while emulsifying the aqueous phase in the organic phase to increase the surface area contact between the organic and aqueous phases. The use of a phase transfer catalyst with a potassium salt-based oxidizing agent improves the recovery efficiency of bromine beyond that reported in prior art methods. The phase transfer catalyst preferably provides a host-guest interaction with potassium ions, where the potassium ions are complexed to multiple complexing sites on the phase transfer catalyst molecule. The complexing sites may include atoms (e.g., O, N, S) that have one or more lone pairs of electrons available for complexing with potassium ions. Preferably, the phase transfer catalyst molecule contains 5 or more complexing sites, more preferably 6 or more complexing sites, and even more preferably 7 or more complexing sites. If the phase transfer molecule is large enough and has a sufficiently large number of complexing sites, one phase transfer molecule can complex with more than one potassium ion. The phase transfer molecule may be acyclic or cyclic, or may contain both acyclic and cyclic moieties. The acyclic molecule or moieties may be linear or branched. The phase transfer molecule is preferably a non-ionic surfactant. The phase transfer catalyst preferably comprises a plurality of ethylene oxide units, preferably 3 to 20 ethylene oxide units. The phase transfer catalyst preferably comprises at least one hydrocarbon chain. Preferably, the phase transfer catalyst comprises a plurality of oxygen atoms to which the potassium ions are complexed. The phase transfer catalyst preferably comprises a polyalkylene oxide ether, such as polyethylene glycol. To enhance solubility in the organic phase, the polyalkylene oxide ether is preferably alkylated.

[0040] In some embodiments, the phase transfer catalyst comprises a Lutensol™ series compound, a Tween™ series compound, Triton™ X-100, polyglycerol polyricinoleate, Poloxamer™ 407, Poloxamer™, Polidocanol™, pentaethylene glycol monododecyl ether, PEG-10 sunflower glyceride, octaethylene glycol monododecyl ether, NP-40, Nonoxynol™-9, Isoceteth™-20, Cetomacrogol™ 1000, or a mixture thereof.

[0041] The oxidant and phase transfer catalyst are preferably present in the aqueous solution in a molar ratio ranging from 1:3 to 100:1, or from 1:3 to 75:1. The oxidant and phase transfer catalyst are preferably present in the aqueous solution in a molar ratio of 1:1, especially when there are sufficient complexation sites on the phase transfer molecule to accommodate only one potassium ion.

[0042] The oxidizing agent and phase transfer catalyst are preferably premixed in the aqueous solution prior to introducing the aqueous solution into the cement reaction medium, although under some circumstances it is possible to introduce the oxidizing agent and phase transfer catalyst separately to the cement-containing reaction medium, preferably by adding the phase transfer catalyst first, followed by the oxidizing agent. The oxidizing agent and phase transfer catalyst are preferably added to the reaction medium prior to introducing the halogenating agent.

[0043] The concentration of oxidizing agent present in the reaction medium is preferably at least 0.06 moles of oxidizing agent per mole of halogenating agent, or at least 0.1 moles of oxidizing agent per mole of halogenating agent. The concentration of oxidizing agent present in the reaction medium is preferably 0.2 to 5 moles of oxidizing agent per mole of halogenating agent, more preferably 0.25 to 4 moles, even more preferably 0.5 to 3 moles. The desired concentration of oxidizing agent is a function of the desired halogenation time. At a halogenation time of 5 minutes, 0.5 to 2 moles of oxidizing agent per mole of halogenating agent, for example 2 moles, are preferred. A lower concentration of oxidizing agent can be compensated for by a longer halogenation time. Adjustment of the stirring speed of the reaction medium can result in an improvement of the efficiency of the halogenation.

[0044] In the process of the present invention, all or a portion of the halogenating agent may comprise hydrogen halide (HX) added to the aqueous phase, which may act as a source of halogenating agent since HX is converted to molecular halogen (X2) by the oxidizing agent in the aqueous phase. EXAMPLES

[0045] Scheme 1 shows an example of a method for producing a halogenated isoolefin copolymer. As shown in Scheme 1, using Br2 as the halogenating agent, KHSO5 as an effective oxidizing agent, and Lutensol™ TO5 as the phase transfer catalyst, the oxygen atoms, which are complexing sites on the phase transfer catalyst, form ion-dipole interactions with the potassium ions of KHSO5. In addition, HSO5 - Hydrogen-bonding interactions are formed between the oxidant and both the oxygen and hydroxyl hydrogen atoms of the phase transfer catalyst. Thus, the phase transfer catalyst can extract the oxidant from the aqueous phase and oxidize the HBr produced in the organic phase back to Br2. In addition, bromide ions that migrate to the aqueous phase can be oxidized by the oxidant to reform Br2 and preferentially migrate back to the organic phase. Thus, the efficiency of bromine utilization in the bromination reaction can be increased.

[0046] [ka]

[0047] Materials and Methods Isobutylene-isoprene polymer (IIR) and epoxidized soybean oil (ESBO) were obtained from ARLANXEO (based in Sarnia, Ontario, Canada). The remaining materials were used as received: potassium peroxymonosulfate (Oxone™ with >4 wt% active oxygen, Sigma-Aldrich), potassium bromate (Sigma-Aldrich), sodium hypochlorite (10-15% available chlorine), Lutensol™ TO3 (BASF), Lutensol™ TO5 (BASF), Lutensol™ TO8 (BASF), Tween™ 20 (Taiko), hexane (VWR), isopentane (Sigma-Aldrich), sodium hydroxide (VWR), 99.99% bromine (Sigma Aldrich), 30 wt% hydrogen peroxide (Sigma-Aldrich), 32 wt% peracetic acid solution (Sigma-Aldrich), calcium stearate (Alfa Aesar), and Irganox™-1010 (BASF).

[0048] Bromination Reaction 250 g of isobutylene-isoprene copolymer (butyl rubber, IIR) was cut into small pieces and added to a 5 L jacketed reactor equipped with an overhead stirrer and pre-charged with "X" mL of hexane or isopentane. The stirring speed was set at 150 rpm while the substrate pieces were added to the reactor. The solution was stirred for 24 hours to completely dissolve the butyl rubber. After the isobutylene-isoprene copolymer was completely dissolved, "Y" mL of water was added to the reactor by pipette to obtain a butyl rubber cement. In examples where an oxidizing agent was used for bromine recovery, the oxidizing agent was first dissolved in "Z" mL of water, and the resulting aqueous solution was then added to the reactor. In examples where both a phase transfer catalyst and an oxidizing agent were used, the phase transfer catalyst and oxidizing agent were first dissolved in "Z" mL of water, and the resulting aqueous solution was then added to the reactor. The amounts of oxidizing agent and phase transfer catalyst are given in the examples. The values ​​of X, Y, and Z are selected to obtain a butyl rubber cement having the water content in the examples below.

[0049] The reactor was heated by setting a circulating bath connected to the jacketed reactor at the desired temperature and the butyl rubber cement was stirred at 350 rpm for 30 minutes at the desired temperature shown in the examples. Bromine (Br2) (2.15 mL, 6.71 g, 0.042 mol) was then added via syringe and the reaction was stirred for 1 hour.

[0050] Over the course of 1 hour, at 5, 20, 40, and 60 minutes, 10 mL samples of the reaction medium were extracted by pipette and added to a vial containing 10 mL of 2.5 M NaOH, and the vial was immediately vigorously stirred to quench residual bromine, HBr, and oxidant. The halogenated polymer samples in vials were then collected by precipitating the polymer solution in ethanol and drying the precipitate under vacuum at 60° C. for 48 hours.

[0051] After 1 hour, a predetermined amount of 2.5M NaOH solution was added to the remaining reaction medium to quench the reaction. An additional 250 mL of water was added to aid mixing. The mixture was continued to stir at 350 rpm for 5 minutes. An additional 1 L of water was added and stirred at 350 rpm for an additional 5 minutes. The stirring was reduced to 150 rpm and stirred for an additional 5 minutes. The reactor stirring was stopped and the aqueous phase was drained through the bottom drain valve. The brominated isobutylene-isoprene copolymer cement was washed with additional water until the pH was 7 to remove residual inorganic salts. A solution of polymer stabilizer in hexane (4.52 g calcium stearate, 0.125 g Irganox™-1010, and 3.25 g ESBO) was added to the reactor and the cement was stirred for 5 minutes. The cement was drained and steam coagulated using low pressure steam for approximately 1 hour. Small pieces of brominated polymer sample were cut from the final product and dried overnight in a vacuum oven at 60°C.

[0052] 1 The microstructure and bromine content of the dried samples were analyzed using 1 H-NMR spectroscopy.

[0053] Bromine Utilization Calculation Bromine utilization in a bromination process can be measured using the Bromine Atom Efficiency (BAE), which is given by the following equation:

[0054]

number

[0055] The Br atoms on the polymer are 1 The Br atoms derived from the bromine added to the reaction are calculated by the volume of bromine used in the reaction. From the formula, it is clear that ideal conditions result in 50% BAE, with 50% of the Br being in the waste HBr. Thus, the theoretical maximum percentage of bromine present in the reaction mixture that can be introduced into the butyl rubber polymer is 50%. However, in practice, the BAE is usually less than 45%, for example 30-45%, or 35-45%.

[0056] In some past methods (e.g., US Pat. No. 3,018,275 and US Pat. No. 5,681,901), bromine utilization is measured using a molecule of molecular bromine added to the reaction, resulting in a numerical result that is twice the BAE since there are two bromine atoms per molecule of molecular bromine. Additionally, these past methods use X-ray diffraction to estimate the amount of Br bound to the Br polymer. However, this method also measures NaBr that is trapped within the polymer matrix resulting from the neutralization process. The trapped NaBr does not necessarily measure the amount of Br chemically bound to the polymer, and generally gives a bromine utilization efficiency number that is higher than the actual efficiency.

[0057] Stability of potassium peroxymonosulfate The temperature stability of potassium peroxymonosulfate in aqueous solution was determined to evaluate its suitability as an oxidizing agent to recover bromine in the bromination of butyl rubber.

[0058] 10 mL of 0.1 mg / L potassium peroxymonosulfate solution in water was placed in a water bath preheated to 45° C. At various time intervals, 1.0 mL of 0.1 g / mL potassium peroxymonosulfate solution in water was added to a tared 250 mL Erlenmeyer flask and the mass of the solution was recorded. The solution was then titrated against a standard 0.1 N sodium thiosulfate solution. The titration procedure was based on the Oxone™ data sheet as described below:

[0059] 75 mL of deionized water, 10 mL of 20% (v / v) sulfuric acid, and 10 mL of 25% (w / w) potassium iodide solution were added to a 250 mL Erlenmeyer flask containing 1.0 mL of 0.1 mg / mL aqueous potassium peroxymonosulfate solution. The sample was immediately titrated with 0.1 N sodium thiosulfate solution to a light yellow color. Then, 3 mL of starch indicator solution was added, and the solution turned deep blue. The titration was continued to a colorless endpoint lasting at least 30 seconds. The active oxygen content was calculated according to the following formula:

[0060]

number

[0061] where mLthio is the volume of the sodium thiosulfate solution and Nthio is the normality of the sodium thiosulfate solution.

[0062] The results are shown in Figure 1, which shows that the active oxygen is 5 wt%, consistent with the technical data sheet from the supplier, and that there is no change in the active oxygen within 1 hour. Thus, potassium peroxymonosulfate is stable over the time of the butyl rubber bromination process at a temperature of 45°C.

[0063] Example 1 Example 1: Effect of potassium peroxymonosulfate on the bromination of IIR The bromination reaction was carried out as described above, where the amount of butyl rubber (IIR) was 20 wt% based on the total mass of the reaction medium, and the amount of water added was 5 wt% based on the total mass of the reaction medium. The unsaturation of the IIR was 1.78 mol%.

[0064] Process P1 was a control, in which no oxidant was added and therefore no bromine recovery was attempted. Process P2 utilized 6.4 g of potassium peroxymonosulfate as the oxidant to recycle bromine, achieving a molar ratio of oxidant:Br2 of 1:2, with 0.5 equivalents of oxidant per bromine molecule. Process P3 utilized 6.4 g of potassium peroxymonosulfate as the oxidant and 120 mg of Lutensol™ TO5 as the phase transfer catalyst (PTC). Lutensol™ TO5 is an isotridecyl alcohol polyoxyethylene ether, which is a derivative of polyethylene glycol (PEG). Table 2 shows the results for samples extracted from the reaction medium at the 60 minute time mark for each of the processes P1, P2 and P3.

[0065] As can be seen in Table 2, comparing P1 and P2, when only 0.5 equivalents of potassium peroxymonosulfate were used as the oxidant, the functional Br increased from 0.61 mol% to 0.72 mol% at the 60 minute mark, indicating that bromine recycling is occurring in the presence of potassium peroxymonosulfate oxidant. However, the inclusion of the phase transfer catalyst Lutensol™ TO5 further increased the functional Br to 0.85% (P3), which is an 18% improvement over potassium peroxymonosulfate alone.

[0066] [Table 2]

[0067] The functional group Br was determined as a function of reaction time by analyzing samples for each of processes P1, P2, and P3 taken at the 5, 20, 40, and 60 minute time marks. Figure 2 shows that the functional group Br does not increase with time in the control process (P1, triangles), while the functional group Br increases in both processes P2 (diamonds) and P3 (squares), which use potassium peroxymonosulfate oxidant. The greatest increase in functional group Br with time occurs when the oxidant is complexed with a phase transfer catalyst (P3, squares).

[0068] P2 60 minute mark of brominated butyl rubber 1 The H NMR spectrum was analyzed to see whether the microstructure was the same as that of the P1 brominated butyl rubber sample. As can be seen in Figure 3, the appearance of resonance signals at 5.4 ppm, 5.02 ppm, and 4.34 ppm in the butyl rubber of process P2 suggests the formation of brominated butyl rubber. The integral ratio of a:b:c is 1:1:1, which is also consistent with the chemical structure of P1 brominated butyl rubber. It is known that when potassium peroxymonosulfate is used to epoxidize olefins, a chemical shift of 2.7 ppm is obtained. This peak is the same as that of the P2 sample. 1 H NMR spectrum, indicating that no epoxidized butyl rubber impurity was produced.

[0069] Example 2 Example 2: Water sensitivity of potassium peroxymonosulfate in the bromination of IIR To determine the water sensitivity of potassium peroxymonosulfate oxidant, bromination processes P4 and P5 were carried out as described above except for the changes in conditions shown in Table 3. The IIR unsaturation was 1.78 mol%. At the 60 minute time mark of each process, samples of P4 and P5 were extracted from the reaction medium. As can be seen in Table 3 and Figure 4A, when 240 mg of Lutensol™ TO5 phase transfer catalyst (PTC) was used (sample P4), the functional Br increased to 0.92 mol% compared to 0.85 mol% when 120 mg of Lutensol™ TO5 was used (sample P3 in Table 2). The use of a larger amount of Lutensol™ TO5 also accelerated the bromination and bromine recovery, as the functional bromine level reached a plateau after 20 minutes (see Figure 4A), unlike P3, which required 1 hour for the functional Br to plateau (see Figure 2). It is clear from Table 3 and FIG. 4A that the ability of potassium peroxymonosulfate to recycle bromine is not significantly affected by differences in the amount of water added to the butyl rubber bromination process.

[0070] [Table 3]

[0071] In another experiment, the concentration of added water in the butyl rubber cement was varied from 0 wt% to 25 wt% to realize five different bromination reactions containing 20 wt% IIR, 3.2 g potassium peroxymonosulfate oxidant, 240 mg Lutensol™ TO5 phase transfer catalyst, and 0.042 moles Br2, and the brominations were carried out at 45°C for a period of 60 minutes. Samples were taken at the 5 minute (P6) and 60 minute (P7) marks to determine the bromine atom efficiency (%) of each sample. As can be seen in Figure 4B, the BAE increases slightly between 0 wt% and 10 wt% water added, then gradually decreases back to the same BAE as the 0 wt% water sample. Overall, the ability of potassium peroxymonosulfate to recycle bromine is not significantly affected by the difference in the amount of water added to the butyl rubber bromination process.

[0072] Example 3 Example 3: Effect of amount and type of phase transfer catalyst in the bromination of IIR The effect of the amount of Lutensol™ TO5 on the bromination of IIR was first tested, as shown by bromination processes P8-P10 in Table 4A. The unsaturation of IIR was 1.78 mol%. At the 60 minute mark, increasing Lutensol™ TO5 from 60 mg to 240 mg increased the BAE (P8, P9). Further increasing Lutensol™ TO5 to 480 mg (P10) results in a slight decrease in BAE, but still exceeds process P2, which used twice the oxidant but added no Lutensol™ TO5. Thus, the BAE peaks when 240 mg of Lutensol™ TO5 is used.

[0073] [Table 4]

[0074] Lutensol™ products have the general formula: RO(CH2CH2O) n H, where R is iso-C 13 H 27where n is 3, 5, 6, 6.5, 7, 8, 10, 12, 15, or 20, and n defines the degree of ethoxylation. In Lutensol™ TO3, n is 3. In Lutensol™ TO5, n is 5. In Lutensol™ TO8, n is 8. The structures of the Lutensol™ series compounds are as follows:

[0075] [ka]

[0076] In addition to Lutensol™ TO5, Lutensol™ TO8 and Lutensol™ TO3 were also tried for bromination (P12 and P13 in Table 4B). The results of the experiment at the 60 minute mark are compared with P11, which used Lutensol™ TO5 (P11 is the same experiment as P5). The number of ethylene glycol units in 240 mg of Lutensol™ TO5, 209 mg of Lutensol™ TO8, and 316.3 mg of Lutensol™ TO3 is the same. As shown in Table 4B, the BAE remains unchanged when using Lutensol™ TO8 and Lutensol™ TO3 compared to Lutensol™ TO5. It has been reported that the minimum number of ethylene glycol units to achieve good complexation with potassium ions is 7. However, shorter ethylene glycol chains improve the partitioning of the phase transfer catalyst in the organic phase due to their lower water solubility, which may explain the bromination results when Lutensol™ TO3 is used.

[0077] [Table 5]

[0078] Tween™ 20, also known as PEG(20) sorbitan monolaurate or polysorbate 20, is a non-ionic molecule based on polyethylene glycol. The structures of the Tween™ series compounds are as follows, where w+x+y+z is 20 for Tween™ 20 and 80 for Tween™ 80:

[0079] [ka]

[0080] In the 1 hour reaction, bromination in the presence of Tween™ 20 (P15) suggests that there is a slight improvement in bromine recovery when Tween™ 20 is used instead of Lutensol™ TO5 (P15).

[0081] [Table 6]

[0082] Example 4 Example 4: Effect of the amount of potassium peroxymonosulfate on the bromination of IIR To determine the effect of the amount of potassium peroxymonosulfate oxidant, three sets of brominations are performed: brominations using 20 wt % IIR and 5 wt % water (Table 5A, FIG. 5A), brominations using 20 wt % IIR and 10 wt % water (Table 5B, FIG. 5B), and brominations using 20 wt % IIR and 15 wt % water (Table 5C, FIG. 5C).

[0083] As can be seen in FIG. 5A, compared to P16 where no oxidant was added, P17 and P18 (P18 is the same experiment as P4) show an increase in functional Br and BAE, indicating that bromine recovery occurred. In addition, by reducing the amount of potassium peroxymonosulfate by half, functional Br is not significantly reduced (compare P17 (squares) and P18 (triangles)). Furthermore, only 0.25 equivalents of potassium peroxymonosulfate (i.e., 1:4 molar ratio) are required compared to Br2 to obtain 0.9 mol% functional Br (see P17 (squares)), which compares favorably with the use of peracetic acid (PAA), which requires 0.5 equivalents (1:2 molar ratio) to obtain 0.9 mol% functional Br.

[0084] [Table 7]

[0085] A second set of bromination processes P19, P20, P21, P22 and P23 using 10 wt% were carried out as above, except for the changes in conditions shown in Table 5B. Process P19 is a control process in which no oxidizing agent was used. As can be seen in FIG. 5B, increasing the amount of potassium peroxymonosulfate generally increases the functionality Br. As with the first set of experiments, reducing the amount of potassium peroxymonosulfate by half does not reduce the functionality Br significantly (compare P21 (triangles) and P22 (x)). Furthermore, only 0.25 equivalents of potassium peroxymonosulfate compared to Br2 (i.e., a 1:4 molar ratio) is required to obtain 0.9 mol% functionality Br (see P21 (triangles)).

[0086] [Table 8]

[0087] A third set of bromination processes P24, P25, P26 and P27 using 15 wt% were carried out as above except for the change in conditions shown in Table 5C (P26 is the same experiment as P14). Process P24 is a control process where no oxidizing agent was used. As can be seen in FIG. 5C and Table 5C, increasing the amount of potassium peroxymonosulfate generally increases the functionality Br and BAE. Furthermore, only 0.25 equivalents of potassium peroxymonosulfate compared to Br2 (i.e., 1:4 molar ratio) is required to obtain 0.86 mol% functionality Br (see P26 (diamond)). By comparing the BAE of P17 (46.2%), the BAE of P21 (49.3%) and the BAE of P26 (45.6%), it is clear that the bromine recovery does not decrease when the water concentration increases from 5 wt% to 15 wt%, indicating that the bromine recovery is not affected by the water concentration in the cement, which is consistent with the results of Example 2.

[0088] [Table 9]

[0089] Example 5 Example 5: Effect of cement concentration on the bromination of IIR Butyl rubber cements were obtained from slurry polymerization of isobutene and isoprene in methyl chloride according to known methods to obtain cements with 10 wt% water content and 10-33 wt% butyl rubber (IIR) content. These cements were brominated at 45°C following the procedure described above using 3.2 g potassium peroxymonosulfate and 240 mg Lutensol™ TO5. Figure 6 shows that the bromination efficiency peaks when the IIR concentration is approximately 20 wt%. This result is consistent with the bromination results when peracid is used as the oxidizing agent.

[0090] Process P28: 5 min bromination, cement concentrations 10 wt%, 15 wt%, 20 wt% and 25 wt%, 10 wt% water, 3.2 g potassium peroxymonosulfate, 240 mg Lutensol™ TO5.

[0091] Process P29: 60 min bromination, cement concentrations 10 wt%, 15 wt%, 20 wt% and 25 wt%, 10 wt% water, 3.2 g potassium peroxymonosulfate, 240 mg Lutensol™ TO5.

[0092] Example 6 Example 6: Effect of the formation of oxidant / PTC complexes in the bromination of IIR To determine whether pre-forming the oxidant / phase transfer catalyst complex is important in bromine recovery, bromination process P30 was conducted according to the conditions shown in Table 6, and the bromination process was compared to a control bromination (P1) in which no oxidant or phase transfer catalyst was present. The IIR was 1.78 mol% unsaturation. Process P30 was undertaken as described above, except for the following sequence of steps:

[0093] Process P30: 1) Prepare IIR cement; 2) Dissolve Lutensol™ TO5 in water; 3) Add Lutensol™ TO5 aqueous solution to cement; 4) Stir for 30 minutes and bring to 45° C.; 5) Add solid potassium peroxymonosulfate to cement; 6) Add bromine to cement.

[0094] In practice, the potassium peroxymonosulfate is added to the cement as a solid rather than as part of an aqueous solution, thereby not allowing it much time to complex with the Lutensol™ TO5 before initiating bromination.

[0095] As can be seen in Figure 7, when potassium peroxymonosulfate is added to the cement as a solid (diamonds), the functionality Br is 0.70 mol%, which is less efficient than when potassium peroxymonosulfate is added to the cement as part of an aqueous solution along with a phase transfer catalyst (see Table 2 and P3 in Figure 2). Therefore, in order to maintain higher levels of bromine recovery, it is important to preform the oxidant / PTC complex before addition to the cement.

[0096] [Table 10]

[0097] Example 7 Example 7: Effect of temperature on the bromination of IIR To determine the effect of reaction temperature, bromination processes P31, P32, and P33 (P33 is the same run as P21) were run as described above except for the changes in conditions shown in Table 7. The IIR unsaturation was 1.78 mol%.

[0098] As can be seen in FIG. 8, reaction temperatures of 23° C. (P31, squares), 35° C. (P32, triangles), and 45° C. (P33, diamonds) result in essentially the same bromine recovery, with the functionality Br still significantly exceeding the control without the use of oxidant.

[0099] [Table 11]

[0100] Example 8 Example 8: Comparison of bromination in hexane and isopentane To investigate the effect of the solvent on bromine recovery, two brominations P34 and P35 were carried out in isopentane with water concentrations of 5 wt% and 15 wt%, respectively. Table 8 shows the results for samples extracted from the reaction medium at the 60 minute time mark for each process of P34 and P35. Due to the low boiling point of isopentane, the two brominations were carried out at 23°C. Although slightly less efficient compared to hexane (P31 and P34), both P34 and P35 showed improved BAE when compared to the control runs without added oxidant (P1, P16, and P24).

[0101] [Table 12]

[0102] Example 9 Example 9: Comparison with peracid and hydrogen peroxide To compare the bromine recovery efficiency using potassium peroxymonosulfate (PPMS) with that of peracetic acid (PAA) and hydrogen peroxide (HO), bromination processes P36, P37 and P38 were carried out as described above except for the changes in conditions shown in Table 9. The IIR unsaturation was 1.78 mol%.

[0103] It is apparent from Table 9 that hydrogen peroxide is not nearly as efficient at recovering bromine as potassium peroxymonosulfate in the presence of added water, even when hydrogen peroxide is used in a molar amount more than four times greater than the molar amount of potassium peroxymonosulfate. It is further apparent from Table 9 that peracetic acid must be used in a molar amount twice that of potassium peroxymonosulfate to achieve the same bromine recovery efficiency as potassium peroxymonosulfate.

[0104] [Table 13]

[0105] Example 10 Example 10: + Other oxidizing agents containing In addition to potassium peroxymonosulfate, another K + Potassium bromate KBrOs was investigated as an oxidizing agent. Bromination processes P39 and P40 were carried out as described above except for the changes in conditions shown in Table 10. The IIR unsaturation was 1.78 mol%. Table 10 shows the results for samples extracted from the reaction medium at the 60 minute time mark for each of the P39 and P40 processes. It is clear from Table 10 and Figure 9 that the addition of Lutensol™ TO5 improved bromine recovery compared to using KBrO3 alone. Although KBrO3 provides high bromine recovery efficiency, KBrO3 is much more difficult to handle than potassium peroxymonosulfate. Therefore, potassium peroxymonosulfate is the preferred KBrOs. + It is considered an oxidizing agent.

[0106] [Table 14]

[0107] Example 11 Example 11: Effect of other metal salts as oxidizing agents To determine the effect of sodium salt-based oxidants on bromine recovery in the presence of a phase transfer catalyst, bromination processes P41 and P42 were carried out as described above except for the changes in conditions shown in Table 11. In P42, Lutensol™ TO5 was mixed with 6.5 mL of NaClO and stirred for 5 minutes before the NaClO solution was added to the reaction medium. Bromine was added to the reaction medium immediately after the addition of the NaClO solution. The unsaturation of the IIR was 1.78 mol%.

[0108] As can be seen in Figure 10, the addition of NaClO oxidant alone (P41, squares) and the addition of NaClO oxidant with 240 mg of Lutensol™ TO5 phase transfer catalyst (P42, crosses) result in very similar bromine recovery efficiencies. Thus, the addition of Lutensol™ TO5 does not improve bromine recovery when NaClO is used as the oxidant. Furthermore, although NaClO results in a relatively high bromine recovery efficiency, NaClO is much more difficult to handle than potassium salt-based oxidants and is therefore less desirable.

[0109] [Table 15]

[0110] Upon review of the description, novel features will become apparent to those skilled in the art. However, it should be understood that the claims should not be limited by the embodiments, but should be given the broadest interpretation consistent with the claims and the language of the specification as a whole.

Claims

1. The method includes contacting an unsaturated isoolefin copolymer cement comprising an unsaturated isoolefin copolymer dissolved in an organic solvent with a halogenating agent and an aqueous solution of a potassium salt-based oxidizing agent under halogenating conditions to form a two-phase reaction medium comprising an organic phase and an aqueous phase, wherein the oxidizing agent is capable of converting hydrogen halide to free halogen; A method for producing a halogenated isoolefin copolymer, wherein the oxidizing agent comprises KHSO5, K2S2O8, KBrO, KIO3, KClO3, KClO4, KIO4, compounds which generate the potassium salt-based oxidizing agents listed above, or mixtures thereof.

2. The method of claim 1 , wherein the oxidizing agent comprises potassium peroxymonosulfate.

3. The oxidizing agent is KHSO 5 2. The method of claim 1, comprising:

4. 4. The method according to claim 1, wherein the cement has a water content of 1 wt. % or more, based on the total mass of the cement.

5. 5. The method of claim 4, wherein the water content of the cement is 1.5 wt% or more.

6. The method of claim 4, wherein the water content of the cement is 1-30 wt%.

7. The method of claim 4, wherein the water content of the cement is between 2 and 20 wt%.

8. 8. The method of claim 1, wherein the aqueous solution further comprises a phase transfer catalyst.

9. 9. The method of claim 8, wherein the phase transfer catalyst comprises a molecule having at least seven oxygen atoms available to form a complex with potassium ions.

10. 10. The method of claim 8 or 9, wherein the phase transfer catalyst comprises a polyalkylene oxide ether.

11. The method of claim 8, wherein the phase transfer catalyst comprises a non-ionic surfactant having at least one hydrocarbon chain and from 3 to 20 ethylene oxide units.

12. 12. The process according to any one of claims 8 to 11, wherein the oxidant and phase transfer catalyst are present in the aqueous solution in a molar ratio ranging from 1:3 to 100:

1.

13. 12. The process according to any one of claims 8 to 11, wherein the oxidant and phase transfer catalyst are present in an aqueous solution in a molar ratio of 1:

1.

14. 14. The method of any one of claims 1 to 13, wherein the unsaturated isoolefin copolymer cement is produced by polymerizing at least one isoolefin monomer and at least one copolymerizable unsaturated monomer in an organic diluent and removing the organic diluent and residual monomer by steam flash separation.

15. 15. The method of claim 14, wherein the at least one isoolefin monomer is isobutene and the at least one copolymerizable unsaturated monomer is isoprene, p-methylstyrene or β-pinene.

16. 15. The method of claim 14, wherein the at least one isoolefin monomer is isobutene, the at least one copolymerizable unsaturated monomer is isoprene, and the unsaturated isoolefin copolymer further comprises one or more additional copolymerizable monomers selected from the group consisting of α-methylstyrene, p-methylstyrene, chlorostyrene, cyclopentadiene, methylcyclopentadiene, and indene.

17. 17. The method of any one of claims 14 to 16, wherein the organic diluent comprises methyl chloride.

18. 18. The method of any one of claims 1 to 17, wherein the halogenating agent is Br2.

19. 19. The process of any one of claims 1 to 18, wherein the unsaturated isoolefin copolymer is present in the reaction medium in an amount of 10 to 33 wt %, based on the total weight of the reaction medium.

20. 20. The method of any one of claims 1 to 19, wherein the contacting of the unsaturated isoolefin copolymer cement with the halogenating agent is carried out at a temperature in the range of 20 to 60°C for 1 to 60 minutes.

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