Patent classifications
C07C2/86
Diamondoid fuels
A diamondoid fuel comprising a cage structure including 10, 14, 18, or 22 carbons. The diamondoid fuel also includes one of one to four cyclopropyl groups bonded to the cage structure or two to four functional groups bonded to the cage structure where the functional groups are an alkyl group, an allyl group, a cyclopropyl group, or combinations thereof. Additionally, at least one functional group is an allyl group and at least one functional group is a cyclopropyl group.
Diamondoid fuels
A diamondoid fuel comprising a cage structure including 10, 14, 18, or 22 carbons. The diamondoid fuel also includes one of one to four cyclopropyl groups bonded to the cage structure or two to four functional groups bonded to the cage structure where the functional groups are an alkyl group, an allyl group, a cyclopropyl group, or combinations thereof. Additionally, at least one functional group is an allyl group and at least one functional group is a cyclopropyl group.
Process and catalyst to convert methanol and toluene to styrene
The invention provides methods, catalysts and systems for producing styrene from DME and toluene. Zeolite catalysts comprising potassium, rubidium or cesium and containing at least 0.1 wt % B are described. Methods of making the catalysts are also described.
METHOD FOR FORMING CARBON-CARBON BOND
A method for forming a carbon-carbon bond, wherein a reaction is performed by filling a platinum group metal-supported catalyst into a filling container, and passing a raw material liquid through the platinum group metal-supported catalyst in a continuous circulation manner, and wherein the platinum group metal-supported catalyst is a platinum group metal-supported catalyst in which nanoparticles of a platinum group metal with an average particle diameter of 1 to 100 nm are supported on a non-particulate organic porous ion exchanger formed of a continuous framework phase and a continuous pore phase.
Processes and Systems for Converting Benzene and/or Toluene via Methylation
This disclosure provides an improved process for converting benzene/toluene via methylation with methanol/dimethyl ether for producing, e.g., p-xylene, comprising separating and recycling dimethyl ether from the methylation reaction product mixture effluent to the methylation reactor. High selectivity toward p-xylene, among others, can be achieved.
Processes for Converting Benzene and/or Toluene Via Methylation
This disclosure provides improved processes for converting benzene/toluene via methylation with methanol/dimethyl ether for producing, e.g., p-xylene. In an embodiment, a process comprises contacting a methylation agent feed with an aromatic hydrocarbon feed in the presence of a methylation catalyst in a methylation reactor at increased pressure. Reduced methylation catalyst deactivation can be achieved with increased pressure in the methylation reactor.
MONO-SUBSTITUTED CYCLOPENTADIENES AND METAL CYCLOPENTADIENYL COMPLEXES AND SYNTHESIS METHODS THEREOF
A metal cyclopentadienyl complex has the formula:
##STR00001##
wherein m≥0; M is a Group I, II or III main group metal, alkali or transition metal; C.sub.5H.sub.4 represents a Cp ring where two hydrogens are substituted by M and R(F).sub.m; R(F).sub.m is connected to any one of the carbon atoms of the Cp and selected from a hydrocarbyl, fluorohydrocarbyl, silyl group [SiR′.sub.3], or amino group [—NR.sup.1R.sup.2]. The metal cyclopentadienyl complexes include Li(C.sub.5H.sub.4-2-C.sub.5H.sub.11) (CAS No: 2413046-23-6), K(C.sub.5H.sub.4-2-C.sub.5H.sub.11), Na(C.sub.5H.sub.4-2-C.sub.5H.sub.11), K(C.sub.5H.sub.4-1-F—C.sub.4H.sub.10), K(C.sub.5H.sub.4-1,1,1-3F—C.sub.4H.sub.6), Li(C.sub.5H.sub.4-2-C.sub.4H.sub.9), or In(C.sub.5H.sub.4-2-C.sub.5H.sub.11) (CAS No.: 2364634-67-1).
A mono-substituted cyclopentadiene has the formula:
##STR00002##
wherein m≥0; C.sub.5H.sub.5 represents the Cp ring where one hydrogen is substituted R(F).sub.m; R(F).sub.m is connected to any one of the carbon atoms of the Cp and selected from a hydrocarbyl, fluorohydrocarbyl, silyl group [SiR′.sub.3], or amino group [—NR.sup.1R.sup.2]. The mono-substituted cyclopentadienes include C.sub.5H.sub.5-1-F—C.sub.4H.sub.10, C.sub.5H.sub.5-2-C.sub.5H.sub.11, C.sub.5H.sub.5-2-C.sub.4H.sub.9, or C.sub.5H.sub.5-1,1,1-3F—C.sub.4H.sub.6.
MONO-SUBSTITUTED CYCLOPENTADIENES AND METAL CYCLOPENTADIENYL COMPLEXES AND SYNTHESIS METHODS THEREOF
A metal cyclopentadienyl complex has the formula:
##STR00001##
wherein m≥0; M is a Group I, II or III main group metal, alkali or transition metal; C.sub.5H.sub.4 represents a Cp ring where two hydrogens are substituted by M and R(F).sub.m; R(F).sub.m is connected to any one of the carbon atoms of the Cp and selected from a hydrocarbyl, fluorohydrocarbyl, silyl group [SiR′.sub.3], or amino group [—NR.sup.1R.sup.2]. The metal cyclopentadienyl complexes include Li(C.sub.5H.sub.4-2-C.sub.5H.sub.11) (CAS No: 2413046-23-6), K(C.sub.5H.sub.4-2-C.sub.5H.sub.11), Na(C.sub.5H.sub.4-2-C.sub.5H.sub.11), K(C.sub.5H.sub.4-1-F—C.sub.4H.sub.10), K(C.sub.5H.sub.4-1,1,1-3F—C.sub.4H.sub.6), Li(C.sub.5H.sub.4-2-C.sub.4H.sub.9), or In(C.sub.5H.sub.4-2-C.sub.5H.sub.11) (CAS No.: 2364634-67-1).
A mono-substituted cyclopentadiene has the formula:
##STR00002##
wherein m≥0; C.sub.5H.sub.5 represents the Cp ring where one hydrogen is substituted R(F).sub.m; R(F).sub.m is connected to any one of the carbon atoms of the Cp and selected from a hydrocarbyl, fluorohydrocarbyl, silyl group [SiR′.sub.3], or amino group [—NR.sup.1R.sup.2]. The mono-substituted cyclopentadienes include C.sub.5H.sub.5-1-F—C.sub.4H.sub.10, C.sub.5H.sub.5-2-C.sub.5H.sub.11, C.sub.5H.sub.5-2-C.sub.4H.sub.9, or C.sub.5H.sub.5-1,1,1-3F—C.sub.4H.sub.6.
Device and method for preparing para-xylene and co-producing light olefins from methanol and/or dimethyl ether and toluene
Disclosed are a fast fluidized bed reactor, device and method for preparing para-xylene and co-producing light olefins from methanol and/or dimethyl ether and toluene, with the reactor, device and method being capable of solving or improving the problem of competition between an alkylation reaction and an MTO reaction during the process of producing the para-xylene and co-producing light olefins from toluene and methanol, thus achieving a synergistic effect between the MTO reaction and the alkylation reaction. By controlling the mass transfer and reaction, the competition between the alkylation reaction and the MTO reaction is coordinated and optimized to achieve a synergistic effect, thereby increasing the conversion rate of toluene, the yield of para-xylene and the selectivity of the light olefins. The fast fluidized bed reactor comprises a first reactor feed distributor and a plurality of second reactor feed distributors, the first reactor feed distributor and the plurality of second reactor feed distributors are sequentially arranged along the gas flow direction in a reaction zone of the fast fluidized bed reactor.
Processes for Converting Benzene and/or Toluene Via Methylation
This disclosure provides improved processes for converting benzene/toluene via methylation with methanol/dimethyl ether for producing, e.g., p-xylene. In an embodiment, a process utilizes a methylation catalyst system comprising a molecular sieve catalyst and an auxiliary catalyst. The auxiliary catalyst comprises a metal element selected from Group 2, Group 3, the lanthanide series, the actinide series, and mixtures and combinations thereof. The auxiliary catalyst may comprise the oxide of the metal element. Deactivation of the molecular sieve catalyst can be reduced with the inclusion of the auxiliary catalyst in the methylation catalyst system.