Provided is a method of producing a porous molded body, the method including: the step of obtaining a molded body by molding a raw material that contains from 1 part by mass to 100 parts by mass of a bicarbonate compound (A) represented by AHCO.sub.3 (wherein, A represents Na or K) and from 0 parts by mass to 99 parts by mass of a compound (B) represented by B.sub.nX (wherein, B represents Na or K; X represents CO.sub.3, SO.sub.4, SiO.sub.3, F, Cl, or Br; and n represents an integer of 1 or 2 as determined by the valence of X) (provided that a total amount of (A) and (B) is 100 parts by mass); and the step of obtaining a porous molded body by performing a heat treatment of the molded body in a temperature range of from 100° C. to 500° C. and an atmosphere that contains water vapor in an amount of from 1.0 g/m.sup.3 to 750,000 g/m.sup.3 and thereby thermally decomposing not less than 90% by mass of the bicarbonate compound (A).

Catalysts for producing a branched aliphatic alkene are described. The catalyst can include a catalytic alkali metal or alkali metal composite on a mixed metal oxide support that includes a Column 1 metal and at least one of a Column 3 metal, a Column 4 metal or a lanthanide. The catalyst can have less than 50 wt. % of a metal carbonate. Methods of producing branched aliphatic alkenes by contacting the catalyst of the present invention with an aliphatic alpha olefin are also described.

Catalysts for producing a branched aliphatic alkene are described. The catalyst can include a catalytic alkali metal or alkali metal composite on a mixed metal oxide support that includes a Column 1 metal and at least one of a Column 3 metal, a Column 4 metal or a lanthanide. The catalyst can have less than 50 wt. % of a metal carbonate. Methods of producing branched aliphatic alkenes by contacting the catalyst of the present invention with an aliphatic alpha olefin are also described.

Provided is a method of producing a porous molded body, the method including: the step of obtaining a molded body by molding a raw material that contains from 1 part by mass to 100 parts by mass of a bicarbonate compound (A) represented by AHCO.sub.3 (wherein, A represents Na or K) and from 0 parts by mass to 99 parts by mass of a compound (B) represented by B.sub.nX (wherein, B represents Na or K; X represents CO.sub.3, SO.sub.4, SiO.sub.3, F, Cl, or Br; and n represents an integer of 1 or 2 as determined by the valence of X) (provided that a total amount of (A) and (B) is 100 parts by mass); and the step of obtaining a porous molded body by performing a heat treatment of the molded body in a temperature range of from 100 C. to 500 C. and an atmosphere that contains water vapor in an amount of from 1.0 g/m.sup.3 to 750,000 g/m.sup.3 and thereby thermally decomposing not less than 90% by mass of the bicarbonate compound (A).

A porous formed body (Y) including a porous formed body (X) that satisfies the following (x-1) to (x-3), and an alkali metal carbonate or an alkali metal bicarbonate, in which a content of the alkali metal carbonate or the alkali metal bicarbonate is in a range of from 1 part by mass to 230 parts by mass, with respect to 100 parts by mass of the porous formed body (X), and a production method thereof, an -olefin dimerization catalyst and a production method thereof, and a method of producing an -olefin dimer:

requirement (x-1): a volume of pores with a pore diameter in a range of from 0.01 m to 100 m is from 0.10 mL/g to 1.00 mL/g;

requirement (x-2): a median pore diameter of pores with a pore diameter in a range of from 0.01 m to 100 m is from more than 0.01 m to 10.0 m; and

requirement (x-3): a crushing strength is from 0.7 kgf to 15.0 kgf.

A novel metal organic framework, EMM-33, is described having the structure of UiO-67 and comprising bisphosphonate linking ligands. EMM-33 has acid activity and is useful as a catalyst in olefin isomerization. Also disclosed is a process of making metal organic frameworks, such as EMM-33, by heterogeneous ligand exchange, in which linking ligands having a first bonding functionality in a host metal organic framework are exchanged with linking ligands having a second different bonding functionality in the framework.

A novel metal organic framework, EMM-33, is described having the structure of UiO-67 and comprising bisphosphonate linking ligands. EMM-33 has acid activity and is useful as a catalyst in olefin isomerization. Also disclosed is a process of making metal organic frameworks, such as EMM-33, by heterogeneous ligand exchange, in which linking ligands having a first bonding functionality in a host metal organic framework are exchanged with linking ligands having a second different bonding functionality in the framework.

A method for purifying 1-hexene is disclosed. The method can include contacting a first stream containing 1-hexene and 2-ethyl-1-butene with an isomerization catalyst containing an comprising an alumina, silica-alumina, a zeolite, or an ion exchange resin, or any combinations thereof, under conditions sufficient to selectively isomerize at least a portion of 2-ethyl-1-butene into 3-methyl-2-pentene and form a second stream containing 1-hexene and 3-methyl-2-pentene, and separating the second stream into a third stream containing 1-hexene and a fourth stream containing 3-methyl-2-pentene.

A method for purifying 1-hexene is disclosed. The method can include contacting a first stream containing 1-hexene and 2-ethyl-1-butene with an isomerization catalyst containing an comprising an alumina, silica-alumina, a zeolite, or an ion exchange resin, or any combinations thereof, under conditions sufficient to selectively isomerize at least a portion of 2-ethyl-1-butene into 3-methyl-2-pentene and form a second stream containing 1-hexene and 3-methyl-2-pentene, and separating the second stream into a third stream containing 1-hexene and a fourth stream containing 3-methyl-2-pentene.

Provided is a formed body containing at least one carbonate compound (A1) selected from Na.sub.2CO.sub.3 or K.sub.2CO.sub.3, the formed body having a volume of pores with a pore diameter of from 0.05 m to 10 m of from 0.10 mL/g to 0.30 mL/g and a crushing strength of from 1.8 kgf to 10.0 kgf.