Patent Grant
9156924
The invention is directed to a method for producing highly reactive olefin polymers wherein at least 50 mol. % of the polymer chains have terminal double bonds, and a novel polymerization initiating system for accomplishing same.
The carbocationic polymerization of isobutylene (IB) is the subject of great scientific and industrial interest. The unique properties of polyisobutylene (PIB), a chemically stable fully saturated polymer make it a desirable material with applications ranging from medical devices to ashless (metal-free) dispersants/detergents suitable for use as motor oil and fuel additives. These ashless dispersants/detergents can be characterized as oil soluble surfactants with oligoamine end-groups derived from low molecular weight (number average molecular weight (
Two major industrial methods have been developed to produce low molecular weight IB homo or copolymers with olefinic end groups. The “conventional” method uses a C4 mixture and an aluminum halide based catalyst system and produces polybutenes with high tri-substituted olefinic contents. Due to the low reactivity of the tri-substituted olefinic end groups, polybutenes need to be chlorinated to react with maleic anhydride to give polybutenylsuccinic anhydride, which is subsequently reacted with oligoalkylenimines to yield polybutenylsuccinimide-type ashless dispersant/detergent. The other method employs a pure IB feed stream and a BF3 complex-based catalyst with either alcohols, or ethers in a polymerization reaction run at low temperature, which yields highly reactive PIB (HR PIB) with high exo-olefinic end-group contents. In contrast to the tri-substituted olefins of conventional polybutenes, PIB exo-olefins readily react with maleic anhydride in a thermal “ene” reaction to produce PIB succinic anhydride and subsequently polyisobutenylsuccinimide ashless dispersants. Because the final product does not contain chlorine, HR PIB is more desirable than conventional polybutenes. However, BF3 is difficult to handle and the polymer may contain fluorine. Further, as noted above, this method requires a pure IB feed steam and low temperature (e.g., −30° C.) and therefore results in a more expensive product.
The above-described commercial process for producing HR PIB has been reported by U.S. Pat. No. 5,408,018 (and DE-A 2702604) to Rath. A range of process enhancements were subsequently reported in. U.S. Pat. Nos. 6,407,186, 6,753,389, and 7,217,773 to Rath et al. and U.S. Pat. Nos. 6,846,903, 6,939,943 and 7,038,008 to Wettling et al. A modified process using a different temperature regime and a low residence time was also previously described (e.g., U.S. Pat. Nos. 6,562,913 and 6,683,138 to Baxter et al.). All of these disclosures describe polymerizations carried out with BF3 catalyst and an alcohol or ether co-catalyst. Such catalytic processes can leave residual fluorine in the polymer especially when utilized with the commonly available mixed C4 Raffinate I stream. The presence of even small amounts of fluorine cause problems in downstream functionalization reactors due to the release of HF and therefore require expensive fluorine removal post-treatment.
Many attempts have therefore been made to find other methods for producing HR PIB. For instance PIB with nearly quantitative exo-olefin end groups has been obtained by reacting tert-chloride-terminated PIB (PIB-Cl) with strong bases such as potassium tert-butoxide and alkali ethoxides in refluxing tetrahydrofuran (THF) for 20-24 h, (Kennedy, J. P.; Chang, V. S. C.; Smith, R. A.; Iván, B. Polym. Bull. 1979, 1, 575); quenching living PIB with methallyltrimethylsilane, (Nielsen, L. V.; Nielson, R. R.; Gao, B.; Kops, J.; Iván, B. Polymer 1997, 38, 2528); quenching living PIB with a hindered base (e.g., 2,5-dimethylpyrrole or 1,2,2,6,6-pentamethylpiperidine), (Simison, K. L.; Stokes, C. D.; Harrison, J. J.; Storey, R. F. Macromolecules 2006, 39, 2481); quenching living PIB with an alkoxysilane or an ether compound (Storey, R. F.; Kemp, L. L. U.S. Patent Application Publication, 2009/0318624 A1, Dec. 24, 2009); and reacting living PIB with a mono-sulfide followed by decomposition of the resulting sulfonium salt with a base (Morgan. D. L.; Stokes, C. D.; Meierhoefer, M. A.; Storey, R. F. Macromolecules 2009, 42, 2344). However, all of the above methods are expensive as they involve living cationic polymerization at low temperature in a moderately polar solvent, and employ expensive reactants.
A broad disclosure of halogen-free metal catalysts based on oxides of Groups V and VI of the Periodic Table of Elements was described in U.S. Pat. No. 6,441,110 to Sigwart et al., but these catalysts were heterogeneous and gave poor monomer conversions, with only modest amounts of exo-olefins. Another catalyst system, based on metals from the 3rd to the 12th periods of the periodic system of elements with nitrile ligands and weakly coordinating anions was described in U.S. Pat. No. 7,291,758 to Bohnepoll et al. These catalysts were used only in a polar dichloromethane solution; not in an apolar, all-hydrocarbon media.
More recently it has been reported that AlCl3-OBu2 complexes in conjunction with a range of initiators or adventitious water initiate the polymerization of IB and in polar solvent (CH2Cl2/hexane 80/20 v/v) yield PIB with high exo-olefinic end groups up to 95% in a range of temperatures (−60 to −20° C.) (Vasilenko, I. V.; Frolov, A. N.; Kostjuk, S. V. Macromolecules 2010, 43(13), 5503-5507). Independently, similar results were reported with adventitious water as initiator in conjunction with AlCl3 or FeCl3 dialkyl ether complexes in CH2Cl2 at temperatures ranging from −20 to 20° C. (Lui, Q.; Wu Y.; Zhang, Y.; Yan. P. F.; Xu, R. W. Polymers 2010, 51, 5960-5969). However, due to the need for the polar solvent CH2Cl2 the commercial potential of this method is questionable. AlCl3-OBu2 has been reported to produce PIB with terminal vinylidene bonds in the absence of solvent and without added initiator, or with water as an added initiator (USPG 2011/0201772A1 of König et al.). However, none of the conventional cationic initiators such as alkyl halides, ethers, esters, alcohols and Brønsted acids were found to initiate directly the polymerization in apolar media with AlCl3. Therefore there remains a need for a robust and economic method for the preparation of highly reactive PIB or polybutene in a non-polar hydrocarbon media.
It was previously found that conventional cationic initiators used in conjunction with certain combinations of Lewis acid/Lewis base complexes initiate the polymerization of IB in hydrocarbon solvents at temperatures of −30° C. to +50° C. and provide high yields of highly reactive PIB. More specifically, it was recognized that polymerization of IB in hydrocarbon solvents at temperatures of −30° C. to +50° C. could be initiated, and provide high yields of highly reactive PIB with a catalyst-initiator system comprising a Lewis acid catalyst (MR″Yn) complexed to a Lewis base (B) in an apolar medium.
The affinity of the Lewis acid for the Lewis base was such that the Lewis acid can interact at least partially with a conventional cationic initiator (RX), enabling the formation of R+, which initiated cationic polymerization of isobutylene. The initially complexed Lewis base was capable of effecting rapid deprotonation of the growing carbocation chain to form an exo-olefin prior to isomerization of the cationic chain or diffusion of the base into free solution. If the Lewis base did not complex to the Lewis acid, at least initially, deprotonation of the growing carbocation was not sufficiently rapid relative to isomerization to give the desired high yields of exo-olefin. If the interaction of the Lewis acid and the Lewis base was so strong that it prevented interaction with a conventional initiator, polymerization was be inefficient or did not occur at all. The Lewis acid or Lewis acid-Lewis base complex had to further be capable of interacting with a conventional initiator either in the presence or absence of adventitious water. Catalysts with which monomer conversion is substantially dependent on adventitious water, even in the presence conventional initiators, as evidenced by complete loss of conversion in the presence of a proton trap (e.g., 2,6-ditert-butylpyridine or “DTBP”), were not suitable. In the above systems, suitable Lewis bases were oxygen- and/or sulfur-containing nucleophiles, such as ethers, alcohols, ketones, aldehydes and esters, and sulfur-containing nucleophiles such as thioethers and thioketones.
Although the above polymerization system was found to provide excellent yields of highly reactive PIB, further study found that the yield could be further increased by proper selection the Lewis base and the control of the ratio of Lewis acid to Lewis base used to form the complex.
Lewis acid catalysts useful in the practice of the present invention can be represented by the general formula (MR″mYn), wherein M is selected from Al, Fe, Ga, Hf, Zr and W; preferably Ga or Fe, more preferably Fe; R″ is a hydrocarbyl group, preferably a C1 to C8 hydrocarbyl group, more preferably a C1 to C8 alkyl group; m is 0 or an integer of 1 to 5, preferably 0 or 1, more preferably 0; Y is halogen (F, Cl, Br), preferably either Cl or Br, more preferably Cl, and n is an integer of 1 to 6, preferably 3 to 5; with the proviso that m+n is equal to the valency of M. As used herein, the term “hydrocarbyl” means a chemical group of a compound that contains hydrogen and carbon atoms and that is bonded to the remainder of the compound directly via a carbon atom. The group may contain one or more atoms other than carbon and hydrogen (“hetero atoms”), provided they do not affect the essentially hydrocarbyl nature of the group.
The Lewis base (B) is dihydrocarbyl ether, wherein each hydrocarbyl group is independently selected from C1 to C8 hydrocarbyl. The hydrocarbyl groups of the above Lewis bases are preferably alkyl groups. The hydrocarbyl groups of the ether may be branched, straight chained or cyclic. Where the hydrocarbyl groups of the ether are branched or straight chained, the hydrocarbyl groups are preferably alkyl groups, more preferably C1 to C4 alkyl. One or each of the hydrocarbyl groups of the dihydrocarbyl ether Lewis base is substituted with an electron-withdrawing group, particularly a halogen atom, preferably chlorine.
An “initiator” is defined as a compound that can initiate polymerization, in the presence or absence of adventitious water and in the presence of a proton trap. The initiator of the present invention (RX) comprises a hydrocarbyl R group wherein the carbon linking group R to X is tertiary, benzylic or allylic, which hydrocarbyl group can form a stable carbocation (e.g., t-butyl+), and an X group, which is a halogen.
The polymerization medium must be a substantially or completely apolar medium, such as a mixture of hexanes or saturated and unsaturated C4 hydrocarbons.
In the polymerization process of the present invention, the feedstock may be pure isobutylene or a mixed C4 hydrocarbyl feedstock containing isobutylene, such as a C4 cut resulting from the thermal or catalytic cracking operation of, for example, naphtha. Thus, suitable feedstocks will typically contain at least 10%, and up to 100% isobutylene, by mass, based on the total mass of the feed. In addition to isobutylene, conventional C4 cuts suitable for use as feedstocks that are of industrial importance typically will contain between about 5% and about 50% butene-1, between about 2% and about 40% butene-2, between about 2% and about 60% iso-butane, between about 2% and about 20% n-butane, and up to about 0.5% butadiene, all percentages being by mass, based on the total feed mass. Feedstocks containing isobutylene may also contain other non-C4 polymerizable olefin monomers in minor amounts, e.g., typically less than 25%, preferably less than about 10%, and most preferably less than 5%, such as propadiene, propylene and C5 olefins. The C4 cut may be purified by conventional means to remove water, polar impurities and dienes.
The term “polybutene”, as employed herein is intended to include not only homopolymers of isobutylene, but also copolymers of isobutylene and one or more other C4 polymerizable monomers of conventional C4 cuts as well as non-C4 ethylenically unsaturated olefin monomers containing 5 carbon atoms, provided such copolymers contain typically at least 50 mass %, preferably at least 65 mass %, and most preferably at least 80 mass % isobutylene units, based on the polymer number average molecular weight (
The Lewis acid and Lewis base can be complexed by, for example, dissolving the Lewis acid in a solvent (e.g., dichloromethane or 1,2-dichloroethane) to form a solution and then adding the Lewis base to the solution, while the solution is stirred. The complex may be added to the polymerization medium with the solvent; alternatively, the solvent may be removed prior to the addition of the complex to the polymerization medium.
The molar ratio of Lewis acid to Lewis base in the complex will typically be maintained within a range of from about 1:0.5 to about 1:2, preferably from about 1:0.7 to about 1:1.5, more preferably from about 1:0.9 to about 1:1.4, such as from about 1:1 to about 1:1.3.
The amount of the Lewis acid-Lewis base complex employed in the process of the present invention can be controlled, in conjunction with the concentration of initiator and monomer, reaction time and temperature, to achieve the target
The initiator will typically be employed in an amount sufficient to contact the butene monomer in a liquid phase reaction mixture at a concentration of millimoles of initiator per liter of medium, and independent from the amount of Lewis acid-Lewis base complex, of from about 1 mM to about 200 mM, preferably from about 5 mM to about 100 mM, and more preferably from about 10 mM to about 50 mM, such as from about 10 mM to about 30 mM.
The polymerization reaction can be conducted batch-wise, semi-continuously, or continuously. On an industrial scale, the polymerization reaction is preferably conducted continuously. Conventional reactors, such as tubular reactors, tube-bundle reactors or loop reactors, or tube or tube-bundle reactors with continuous circulation of the reaction material, may be used.
The polymerization reaction is conducted in the liquid phase to induce linear or chain-type polymerization, as opposed to ring or branch formation. Thus, if a feed is used that is gaseous under ambient temperature, it is preferred to control the reaction pressure and/or dissolve the feed in an inert solvent or liquid diluent, in order to maintain the feed in the liquid phase. Typical C4 cuts comprising the feed are liquid under pressure and do not require a solvent or diluent. Typical diluents suitable for use with the process include C3 to C6 alkanes, such as propane, butane, pentane, isobutane and the like.
The Lewis acid-Lewis base complex is typically introduced into the reactor as a liquid partially or completely dissolved in a solvent, or as a solid. Polymerization is preferably conducted at a pressure sufficient to maintain the C4 feed in a liquid state at the reaction temperature, or at higher pressures. The initiator may be introduced to the monomer feed or the reaction mixture in liquid form together with the Lewis acid-Lewis base complex or, preferably, is introduced to the monomer feed or the reaction mixture in liquid form by a line separate from the Lewis acid-Lewis base complex addition line.
The liquid phase reaction mixture temperature is controlled by conventional means to be typically from about −30° C. to about +50° C., preferably from about −10° C. to about +30° C., more preferably from 0° C. to about +20° C., such as from 0° C. to about +10° C.
The residence time of the butene to be polymerized may be from about 5 seconds to several hours, but will typically be from about 1 to about 300 minutes, such as 2 to about 120 minutes, preferably from about 5 to about 60 minutes.
In order to insure even distribution of the catalyst within the reactor, turbulent flow of the reactor contents can be generated by mixing, or with suitable baffles, such as baffle plates or oscillating baffles, or by dimensioning the reactor tube cross sections so that a suitable flow velocity is established.
The process of the present invention is typically conducted in a manner achieving an isobutylene conversion in the range of from about 20% up to about 100%, preferably from about 50% to about 100%, and more preferably from about 70% to about 100%. The combined use of temperature control and catalyst feed rate permits formation of polybutenes having a
Once the target molecular weight of the polymer is achieved, the polymer product can be discharged from the reactor and passed into a medium that deactivates the polymerization catalyst and terminates the polymerization. Suitable deactivation media include water, amines, alcohols and caustics. The polyisobutylene product can then be separated by distilling off the remaining C4 hydrocarbons and low molecular weight oligomers. Preferably residual amounts of catalyst are removed, usually by washing with water or caustic.
This invention will be further understood by reference to the following examples, which are not intended, and should not be construed as listing all possible embodiments within the scope of the invention.
Polymerizations were carried out under a dry nitrogen atmosphere in an MBraun 150-M glove box (Innovative Technology Inc., Newburyport, Mass.) Isobutene (IB) was condensed and distributed to the polymerization reactors, screw top culture tubes (75 ml) at −30° C. Polymerizations were conducted in hexanes co-initiated with the appropriate FeCl3 concentration with a monomer concentration of 1M, at 0° C. After a predetermined time, polymerization was terminated by addition of 0.2 mL methanol. The polymer was recovered and purified by re-precipitation from NH4OH solution. Conversions were determined by gravimetric analysis.
Preparation of Lewis Acid (LA/Ether Complexes)
FeCl3.dialkyl ether complexes were prepared at room temperature just before the polymerization of IB. In a glovebox DCM was added to FeCl3, which had been previously weighed and sealed in a 20 mL screw-cap vial with a Teflon seal. Next, an equimolar amount of the appropriate ether was added drop-wise via a syringe to the sealed vial containing the Lewis acid while stirring to form a 1.0 M Lewis acid/ether complex solution.
Characterization
Number average molecular weight (
Nuclear Magnetic Resonance
Proton nuclear magnetic resonance (1H NMR) spectra were recorded on a Bruker 500 MHz spectrometer using CDCl3 as solvent (Cambridge Isotope Laboratory, Inc.). The polyisobutene (PIB) end group content was determined by 1H NMR as previously reported (see Kumar, R.; Dimitrov, P.; Bartelson, K. J.; Faust, R., Macromolecules 2012, 45, 8598-8603).
Results
While not wishing to be bound by any specific theory, it is suggested that one possible polymerization scheme for the polymerization of IB with FeCl3 is as shown below:
Since steric and electronic effects impact the rate of ionization and chain transfer (β-proton abstraction followed by proton transfer to IB), polymerization rate, molecular weight and exo-olefin are all affected by the selection of the R and R′ groups of ROR′. Further, steric and electronic effects may also affect the equilibrium constant of the Lewis acid with the ether.
Complex formation between FeCL3 and the ethers shown below was studied in 1.0 M CH2Cl2 solutions at room temperature using ATR FT-IR spectroscopy. Previous studies of the complex formation of FeCl3 and diisopropyl ether (ether 1) by ATR FT-IR indicated that only a 1:1 complex is formed, as evidenced by the presence of free ether when excess amounts of ether are added relative to FeCl3 (see Liu, Q.; Wu, Y.; Yan, P.; Zhang, Y; Xu, R., Macromolecules 2011, 44, 1866-1875; see also Kumar, R.; Dimitrov, P.; Bartelson, K. J.; Emert, J.; Faust, R., Macromolecules 2012, 45, 8598-8603).
Consistent with the previously reported results discussed supra, the 1:1 complex of FeCl3 with diisopropyl ether (ether 1) did not show any un-dissolved FeCl3, which is indicative of complete complexation. The 1:1 complex of FeCl3 and (2-chloroethyl) ethyl ether (ether 2) did not show un-dissolved FeCl3, while the corresponding complex of FeCl3 and bis-(2-chloroethyl)ether (ether 3) did. Upon increasing the ratio of FeCl3:ether 3 to 1:1.13, un-dissolved FeCl3 could no longer be visually detected in the complex solution. The 1:1 complex of FeCl3.ether 4 showed some un-dissolved FeCl3 and was similar in appearance to the 1:1 complex of FeCl3 and ether 3. The shifting of the ether IR signature to lower wavelengths is consistent with a complexation event; complexation causes the lengthening of the C—O bond of the ether, which causes the observed wavelength shift.
The above observations can all be interpreted in terms of different complexation equilibria with different ethers. Complexes that do not show un-dissolved FeCl3 at 1:1 FeCl3 to ether oxygen stoichiometry i.e., ethers 1 and 2, clearly have an equilibrium constant that favors complexation. Conversely, complexes that do show un-dissolved FeCl3; complexes with ethers 3 and 4 have lower complex equilibrium constants. In the cases of ethers 4 and 4, the lower equilibrium constant of complexation can be attributed to electronic effects, as the presence of the two electron withdrawing chlorine atoms significantly decreases the electron density of the ether oxygen.
Solubility studies were conducted on the ethers 1, 2, 3 and 4 using a simple centrifuge experiment simulating polymerization conditions. A complex was prepared as a 1.0 M solution in dichloromethane (DCM) in a 30 mL centrifuge tube. The centrifuge was then set to the appropriate temperature (0° C.) and an appropriate amount of hexane was added to the centrifuge tube such that the complex concentration was 0.2 M. The centrifuge tube was allowed to equilibrate to the appropriate temperature in the centrifuge before it was spun at 3750 rpm for 10 minutes. Upon completion, an aliquot of the centrifuged solution was transferred to a round bottom flask, the solvent and excess ether (if any still remained) was removed, and the residue was weighed. From this data, the amount of complex dissolved in the entire solution was calculated (see Table 1).
aBased on ATR FT-IR studies in DCM.
bBased on solubility studies in hexanes
The 1:1 complexes of FeCl3 with chlorinated ethers 2 and 3 showed decreased solubility compared to ether 1. The lower concentration of 1:1 FeCl3.ether 3 complex can also be attributed to incomplete complex formation due to the reduced electron density on the oxygen of this particular ether. This phenomenon was more pronounced in the case of the 1:1 FeCl3.ether 4 complex, with which the concentration of the complex in the reaction system was only 0.00044 M.
The above solubility data were then correlated with the results from polymerizations using the various complexes (Table 2).
n
n
cGravimetric conversion.
dDetermined by 1H NMR spectroscopy.
e[PIB] = [IB] × 56.11 × (conv./
fAll values averaged from multiple runs.
When the polymerization was coinitiated with FeCl3 complexes prepared with ether 2 or 3, which possess an electron withdrawing chlorine atom(s), increased conversion (>60%), but slightly lower exo-olefin content (≈60%) was obtained, as compared to those obtained with FeCl3.ether 1 (entries 6 and 7 vs. entry 5). The higher conversion was obtained despite the lower soluble complex concentration when using ethers 2 and 2 in solution as compared to ether 1. Similarly, the 1:1 complex of FeCl3.ether 4 provided higher monomer conversion (but with lower exo-olefin content), even though the concentration of soluble complex was extremely low (entry 8). These results contrast with the absence of polymerization reported previously with diethyl ether (see Kumar, R.; Dimitrov, P.; Bartelson, K. J.; Emert, J.; Faust, R., Macromolecules 2012, 45, 8598-8603).
The effect of the stoichiometry of FeCl3/ether stoichiometry and FeCl3.ether complex concentration are shown in Tables 3 and 4, respectively.
n
n
cGravimetric conversion.
dDetermined by 1H NMR spectroscopy.
e[PIB] = [IB] × 56.11 × (conv./
fAll values averaged from multiple runs.
The polymerization conversion was found to decrease in the presence of excess ether 1 (entry 11), but remain essentially unchanged in the presence of excess FeCl3 (entry 9). In contrast, with both FeCl3.ether 2 and FeCl3.ether 3 complexes, there was no significant change in conversion or exo-olefin content in the studied range of FeCl3:ether ratios. (entries 12 through 21). This can be attributed to the presence of the electron withdrawing chlorine atoms on ethers 2 and 3.
n
n
cGravimetric conversion.
dDetermined by 1H NMR spectroscopy.
e[PIB] = [IB] × 56.11 × (conv./
fAll values averaged from multiple runs.
Decreasing the concentration of the complex did not have a significant effect on the outcome of the polymerization, although a slight decrease in conversion and slight increase in exo-olefin content was observed (entries 22 to 27). These results attest to the robustness of the catalyst/initiation system.
A comparison of the kinetics of IB polymerization initiated by t-BuCl/FeCl3.ether in hexanes at 0° C. is shown, in graphical form, in
The impact of the proton trap 2,6-ditert.-butylpyridine (DTBP) on the polymerization of IB initiated by 2-chloro-2,4,4-trimethylpentane (TMPCl) or t-BuCl and coinitiated by FeCl3.ether complexes is shown in Table 5.
n
n
36f
cGravimetric conversion.
dDetermined by 1H NMR spectroscopy.
e[PIB] = [IB] × 56.11 × (conv./Mn,NMR).
fAll values averaged from multiple runs.
It was previously found that in the absence of initiator and DTBP, the use of the FeCl3.ether 1 system resulted in ≈29% IB conversion (see Kumar, R.; Dimitrov, P.; Bartelson, K. J.; Emert, J.; Faust, R., Macromolecules 2012, 45, 8598-8603). In contrast, in the absence of initiator and DTBP, the use of the 1:1 FeCl3.ether 2 complex and the 1:1.35 FeCl3.ether 3 complex resulted in 56% and 86% conversion, respectively (entries 32 and 37). The substantially higher rates of polymerization for both ethers 2 and 3, compared to ether 1, and the higher rate of polymerization for ether 3 compared to ether 2 can be explained by the fact that the nucleophilicity of these ethers increases in the order ether 3<ether 2<ether 1. Thus, the ether is more easily displaced from the complex in the case of ether 3, which allows for the faster ionization of t-BuCl.
In the presence of DTBP at 0.005 M, 5% and 36% conversion was reached at 20 minutes (entries 33 and 38). At 0.01M DTBP, polymerization was absent in the case of ether 2, however 24% conversion was still obtained with ether 3 (entries 34 and 39). It is noted that the ether moiety was not observed in the 1H NMR spectrum of the product, and thus, ether 3 is not an initiator.
The molecular weights were generally high with ether 3 as opposed to ether 2 due to the fact that ether 3 is less basic than ether 2 and thus, there is a decrease in proton abstraction from the growing chain end, which consequentially leads to a polymer with a higher molecular weight. The addition of t-BuCl increases conversion and, furthermore, PIB with an exo-olefin content of ≈60 to 70% was obtained (entries 35 and 40). Conversions, molecular weights and exo-olefin contents were similar for both t-BuCl and TMPCl (entry 35 vs. 42 and entry 40 vs. 44).
While certain representative embodiments and details have been provided to illustrate the invention, it will be apparent to the skilled artisan that various product and process changes from those disclosed herein may be made without departing from the scope of the present invention. The appended claims define the scope of the invention
All cited patents, test procedures, priority documents, and other cited documents are fully incorporated by reference to the extent that such material is consistent with this specification and for all jurisdictions in which such incorporation by reference is permitted.
Certain features of the present invention are described in terms of a set of numerical upper limits and a set of numerical lower limits. This specification discloses all ranges formed by any combination of these limits. It is to be understood that the upper limits and lower limits, as well as range and ratio limits set forth herein may be independently combined, and that all combinations of these limits are within the scope of the invention unless otherwise indicated.
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| Number | Date | Country | |
|---|---|---|---|
| 20140275453 A1 | Sep 2014 | US |
