Abstract: This disclosure relates to naphthalene-1,8-dicarboxylate ester compounds, lubricating oil base stocks comprising naphthalene-1,8-dicarboxylate ester compounds, lubricating oil compositions comprising such base stocks, and method of making such base stocks. The lubricating oil base stocks comprising naphthalene-1,8-dicarboxylate ester compounds exhibit desirable lubricating properties such as polarity.

Abstract: Methods are provided for converting lignin-containing biomass into compounds that are more readily processed to form fuel and/or chemical products. The methods can allow for removal of at least a portion of the oxygen in lignin, either during or after depolymerization of lignin to single ring aromatic compounds, while optionally reducing or minimizing aromatic saturation performed on the aromatic compounds. The methods can include use of quench solvent to control reactions within the product stream from a pyrolysis process and/or use of a solvent to assist with hydroprocessing of lignin, lignin-containing biomass, or a pyrolysis oil.

Abstract: A diester of a fused ring compound of the formula (I): wherein the R1 to R6 substituents are H or ester moieties having C1 to C20 alkyl chains, but when both fused rings are aromatic and R3 and R4 are ester moieties, the alkyl chains are not C5 or C8, and polymer compositions containing the fused ring compound.

Abstract: Provided are compounds and processes of making and using such compounds of the formula: Wherein R=C4 to C15 linear or branched alkyls wherein R is a linear or branched alkyl residue of a C4 to C15 alcohol. Such compounds provide advantageous properties when used as plasticizers in polymer compositions.

Abstract: This invention relates to a continuous homogeneous solution phase polymerization process comprising contacting, in an evaporative reactor system at a temperature of 50° C. or more and a pressure of 100 kPa or more, a catalyst system, optionally, a hydrocarbon diluent, optionally, scavenger, and one or more monomer(s) to form a homogeneous polymerization medium, where the polymer product is dissolved in the reaction medium at 10 wt % or more (based upon the weight of the polymer present in the effluent at the exit of the reactor) and the catalyst system is dissolved in the reaction medium, and where the catalyst system comprises an activator and a coordination catalyst precursor compound and where all or part of the polymerization medium is evaporated during the polymerization.

Abstract: Disclosed herein is a process for producing phenol. The process includes oxidizing at least a portion of a feed comprising cyclohexylbenzene to produce an oxidation composition comprising cyclohexyl-1-phenyl-1-hydroperoxide. The oxidation composition may then be cleaved in the presence of an acid catalyst to produce a cleavage reaction mixture comprising the acid catalyst, phenol and cyclohexanone. At least a portion of the cleavage reaction mixture may be neutralized with a basic material to form a treated cleavage reaction mixture. In various embodiments, the treated cleavage reaction mixture contains no greater than 50 wppm of the acid catalyst or no greater than 50 wppm of the basic material.

Abstract: Methods are provided for producing lubricant base stocks from deasphalted oils formed by sequential deasphalting. The deasphalted oil can be exposed a first deasphalting process using a first solvent that can provide a lower severity of deasphalting and a second deasphalting process using a second solvent that can provide a higher severity of deasphalting. This can result in formation of at least a deasphalted oil and a resin fraction. The resin fraction can represent a fraction that traditionally would have been included as part of a deasphalter rock fraction.

Abstract: A system for making cyclohexylbenzene starting from benzene and hydrogen includes a first benzene preparation column, a hydroalkylation reactor, a dehydrogenation reactor, a second distillation column for cyclohexylbenzene separation, a third distillation column for cyclohexylbenzene purification, a transalkylation reactor, and a fourth distillation column for separating cyclohexylbenzene from transalkylation effluent. All components are integrated to achieve a high-purity cyclohexylbenzene product produced with a high yield and high overall energy efficiency.

Abstract: In a process for producing phenol, a cleavage feed comprising cyclohexylbenzene hydroperoxide is supplied to a cleavage reaction zone and a cleavage reaction mixture comprising the cleavage feed is contacted in the cleavage reaction zone with a solid acid catalyst under conditions effective to produce a cleavage effluent comprising phenol and cyclohexanone. The cleavage effluent is then divided into at least a cleavage product and a cleavage recycle and the cleavage recycle and a polar solvent is supplied to the cleavage reaction zone to produce the cleavage reaction mixture with the cleavage feed. Preferably, the polar solvent is combined with the cleavage recycle before being charged into the cleavage reaction zone.

Abstract: This invention relates to a continuous homogeneous solution phase polymerization process comprising contacting, in an evaporative reactor system at a temperature of 50° C. or more and a pressure of 100 kPa or more, a catalyst system, optionally, a hydrocarbon diluent, optionally, scavenger, and one or more monomer(s) to form a homogeneous polymerization medium, where the polymer product is dissolved in the reaction medium at 10 wt % or more (based upon the weight of the polymer present in the effluent at the exit of the reactor) and the catalyst system is dissolved in the reaction medium, and where the catalyst system comprises an activator and a coordination catalyst precursor compound and where all or part of the polymerization medium is evaporated during the polymerization.

Abstract: Disclosed herein are methods and apparatus for deactivating a catalyst composition in an reaction product stream. One such method and apparatus contact the catalyst composition with a catalyst-deactivating composition and a diluent in a vapor phase of a product-receiving vessel, wherein the boiling point of the diluent is at least 5.0° C. greater than the boiling point of the catalyst-deactivating composition. Also disclosed are oligomerization systems for producing oligomers.

Abstract: In a process for producing phenol, benzene is reacted with a source of hydrogen containing methane in the presence of a hydroalkylation catalyst under conditions effective to produce a hydroalkylation reaction effluent comprising cyclohexylbenzene, benzene, hydrogen, and methane. A first stream comprising hydrogen, methane, and benzene is removed from the hydroalkylation reaction effluent and the first stream is washed with a second stream containing cyclohexylbenzene to produce a benzene-depleted hydrogen stream containing hydrogen and methane and a wash stream containing cyclohexylbenzene and benzene.

Abstract: In a process for producing cyclohexylbenzene, hydrogen and benzene are introduced to a first hydroalkylation reaction zone which contains a hydroalkylation catalyst and which is operated under at least partly liquid phase conditions sufficient to effect hydroalkylation of benzene to produce a mixed liquid/vapor phase effluent comprising cyclohexylbenzene and unreacted benzene, wherein at least a portion of the unreacted benzene is in the vapor phase. At least a portion of the effluent is cooled to condense a liquid phase stream containing at least some of the cyclohexylbenzene in the effluent portion and leave a residual stream containing at least some of the unreacted benzene and cyclohexylbenzene. At least a portion of the liquid stream is recycled to the first hydroalkylation reaction zone or to contact the mixed phase effluent exiting the first hydroalkylation reaction zone. Other methods of cooling the reaction effluent are disclosed.

Abstract: In a process for producing cyclohexylbenzene, benzene is contacted with hydrogen in the presence of a hydroalkylation catalyst under hydroalkylation conditions effective to form a first effluent stream comprising cyclohexylbenzene, cyclohexane, and benzene. At least a portion of the cyclohexane from the first effluent stream is then contacted with hydrogen in the presence of a dehydrogenation catalyst under dehydrogenation conditions effective to convert at least some of the cyclohexane into benzene contained in a second effluent stream. At least some of the hydrogen is supplied to the process so as to contact the dehydrogenation zone (e.g., the dehydrogenation catalyst) before contacting the hydroalkylation catalyst.

Abstract: In a process for producing cyclohexylbenzene, benzene is contacted with hydrogen under hydroalkylation conditions effective to form a first effluent stream comprising cyclohexylbenzene, cyclohexane, methylcyclopentane, and unreacted benzene. At least a portion of the first effluent stream is contacted with a dehydrogenation catalyst under dehydrogenation conditions to convert at least a portion of the cyclohexane to benzene thereby forming a second effluent stream. The amount of methylcyclopentane in the second effluent stream is different by no more than 65% of the total amount of the portion of the first effluent stream, said amounts being on a weight basis. A methylcyclopentane-containing stream is removed from either the first or the second effluent stream and at least a portion of the second effluent stream containing benzene is recycled to the hydroalkylation step.

Abstract: Disclosed herein are processes for producing phenol. The processes include oxidizing cyclohexylbenzene to produce an oxidation composition comprising cyclohexyl-1-phenyl-1-hydroperoxide. The cyclohexyl-1-phenyl-1-hydroperoxide in the oxidation composition may undergo a cleavage reaction to produce a cleavage reaction mixture comprising phenol, cyclohexanone and at least one contaminant. The cleavage reaction mixture may be contacted with a basic material to convert at least a portion of the contaminant to a converted contaminant, thereby producing a modified reaction mixture.

Abstract: Methods are provided for converting lignin-containing biomass into compounds that are more readily processed to form fuel and/or chemical products. The methods can allow for removal of at least a portion of the oxygen in lignin, either during or after depolymerization of lignin to single ring aromatic compounds, while optionally reducing or minimizing aromatic saturation performed on the aromatic compounds. The methods can include use of quench solvent to control reactions within the product stream from a pyrolysis process and/or use of a solvent to assist with hydroprocessing of lignin, lignin-containing biomass, or a pyrolysis oil.

Abstract: This invention relates to a dimethylterephthalate production process comprising reacting substituted furan with ethylene under cycloaddition reaction conditions and in the presence of a cycloaddition catalyst to produce a bicyclic ether, dehydrating the bicyclic ether to produce a substituted phenyl, dissolving said substituted phenyl in methanol, and oxidizing and esterifying the substituted phenyl in the presence of an oxidative esterification catalyst to form dimethylterephthalate. Importantly, the process does not include oxidizing the substituted phenyl to form terephthalic acid.

Abstract: A system for producing high-purity phenol and/or cyclohexanone from cyclohexylbenzene oxidation includes a cyclohexylbenzene feed hydrogenation reactor, a bubble column oxidation reactor, a cyclohexylbenzene hydroperoxide concentrator, a cleavage reactor, and a separation and purification sub-system. The components and the integrated system are designed such that high-purity phenol and/or cyclohexanone can be produced at high energy efficiency.

Abstract: A cyclohexane dehydrogenation process comprising a step of providing, as a benzene-containing stream, a vapor phase in equilibrium with a liquid phase at a condensation separation system; supplying benzene, hydrogen, and cyclohexane into a dehydrogenation reactor where at least part of the benzene supplied is from the benzene-containing stream. The use of a condensation separation system enables the control of the partial pressure of benzene in the material fed into the dehydrogenation reactor by controlling the temperature of the vapor phase, and hence the control of hydrogen to benzene molar ratio in the dehydrogenation reactor. The process results in a long life of the dehydrogenation catalyst due to reduced coking.