Systems and methods are provided for forming alkylate from a tertiary alcohol feed. Olefins for the alkylation reaction can be generated from a portion of the tertiary alcohol feed. The tertiary alcohol feed can be obtained, for example, by selective oxidation to convert a portion of an isoparaffin-containing feed into alcohol, such as conversion of isobutane to t-butyl alcohol. The alcohol can then be converted to an alkene, such as conversion of t-butyl alcohol to isobutene, in the alkylation reaction environment in the presence of a solid acid catalyst. The solid acid catalyst can then facilitate dimerization of the alkenes (e.g. isobutene) to form C.sub.8+ olefins (e.g. isooctene). A catalyst having an MWW framework is an example of a suitable solid acid catalyst.

Systems and methods are provided for forming alkylate from a tertiary alcohol feed. Olefins for the alkylation reaction can be generated from a portion of the tertiary alcohol feed. The tertiary alcohol feed can be obtained, for example, by selective oxidation to convert a portion of an isoparaffin-containing feed into alcohol, such as conversion of isobutane to t-butyl alcohol. The alcohol can then be converted to an alkene, such as conversion of t-butyl alcohol to isobutene, in the alkylation reaction environment in the presence of a solid acid catalyst. The solid acid catalyst can then facilitate dimerization of the alkenes (e.g. isobutene) to form C.sub.8+ olefins (e.g. isooctene). A catalyst having an MWW framework is an example of a suitable solid acid catalyst.

Systems and methods are provided for forming alkylate from an isoparaffin-containing feed. Olefins for the alkylation reaction can be generated from a portion of the isoparaffin-containing feed. This can be achieved, for example, by using selective oxidation to convert a portion of isoparaffins into alcohol, such as conversion of isobutane to t-butyl alcohol. The alcohol can then be converted to an alkene, such as conversion of t-butyl alcohol to isobutene, in the alkylation reaction environment in the presence of a solid acid catalyst. The solid acid catalyst can then facilitate alkylation of isoparaffin using the in-situ formed alkenes. A catalyst having an MWW framework is an example of a suitable solid acid catalyst.

Systems and methods are provided for forming alkylate from an isoparaffin-containing feed. Olefins for the alkylation reaction can be generated from a portion of the isoparaffin-containing feed. This can be achieved, for example, by using selective oxidation to convert a portion of isoparaffins into alcohol, such as conversion of isobutane to t-butyl alcohol. The alcohol can then be converted to an alkene, such as conversion of t-butyl alcohol to isobutene, in the alkylation reaction environment in the presence of a solid acid catalyst. The solid acid catalyst can then facilitate alkylation of isoparaffin using the in-situ formed alkenes. A catalyst having an MWW framework is an example of a suitable solid acid catalyst.

A peracetic acid decontamination chemical indicator including a substrate and an indicator composition disposed thereon, where the indicator composition comprises a colorant that changes color when exposed to a peracetic acid solution but does not change color when exposed to a hydrogen peroxide solution, an acidified hydrogen peroxide solution, or an acetic acid solution, and where the indicator composition does not include a transition metal salt or a halogen source, and methods of using the chemical indicator.

A peracetic acid decontamination chemical indicator including a substrate and an indicator composition disposed thereon, where the indicator composition comprises a colorant that changes color when exposed to a peracetic acid solution but does not change color when exposed to a hydrogen peroxide solution, an acidified hydrogen peroxide solution, or an acetic acid solution, and where the indicator composition does not include a transition metal salt or a halogen source, and methods of using the chemical indicator.

A process for forming a concentrated solution, including distilling in a distillation zone comprised of 10 or more theoretical distillation stages, at a pressure of no greater than 300 mm Hg and a reflux ratio (D/L) of at least 1:1, an amount of an initial solution comprised of tert-butyl hydroperoxide (TBHP) in tert-butyl alcohol (TBA) having a TBHP concentration of up to 60 wt. % and a total impurity content greater than 0.01 wt. %, for a time and under distillation conditions to form a concentrated solution comprised of TBHP in TBA; and separating an overhead distillate from the distillation zone so that the concentrated solution thereafter has a TBHP concentration greater than 60 wt. %, a TBA concentration less than 40 wt. %, a water impurity content no greater than 0.1 wt. % and a total impurity content of no greater than 1 wt. %. Related epoxidation catalyst formation and epoxidation processes are also described.

A process for forming a concentrated solution, including distilling in a distillation zone comprised of 10 or more theoretical distillation stages, at a pressure of no greater than 300 mm Hg and a reflux ratio (D/L) of at least 1:1, an amount of an initial solution comprised of tert-butyl hydroperoxide (TBHP) in tert-butyl alcohol (TBA) having a TBHP concentration of up to 60 wt. % and a total impurity content greater than 0.01 wt. %, for a time and under distillation conditions to form a concentrated solution comprised of TBHP in TBA; and separating an overhead distillate from the distillation zone so that the concentrated solution thereafter has a TBHP concentration greater than 60 wt. %, a TBA concentration less than 40 wt. %, a water impurity content no greater than 0.1 wt. % and a total impurity content of no greater than 1 wt. %. Related epoxidation catalyst formation and epoxidation processes are also described.

A process for converting light paraffins to heavier paraffinic hydrocarbon fluids is disclosed. The process involves: (1) oxidation of iso-paraffins to alkyl hydroperoxides and alcohols; (2) conversion of the alkyl hydroperoxides and alcohols to dialkyl peroxides; and (3) radical-initiated coupling of paraffins and/or iso-paraffins using the dialkyl peroxides as radical initiators, thereby forming heavier hydrocarbon products. Fractionation of the heavy hydrocarbon products can then be used to isolate fractions for use as hydrocarbon fluids.

A process for converting light paraffins to heavier paraffinic hydrocarbon fluids is disclosed. The process involves: (1) oxidation of iso-paraffins to alkyl hydroperoxides and alcohols; (2) conversion of the alkyl hydroperoxides and alcohols to dialkyl peroxides; and (3) radical-initiated coupling of paraffins and/or iso-paraffins using the dialkyl peroxides as radical initiators, thereby forming heavier hydrocarbon products. Fractionation of the heavy hydrocarbon products can then be used to isolate fractions for use as hydrocarbon fluids.