WO2006036697A2 - Titanium oxide and alumina alkali metal compostions - Google Patents
Titanium oxide and alumina alkali metal compostions Download PDFInfo
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- WO2006036697A2 WO2006036697A2 PCT/US2005/033823 US2005033823W WO2006036697A2 WO 2006036697 A2 WO2006036697 A2 WO 2006036697A2 US 2005033823 W US2005033823 W US 2005033823W WO 2006036697 A2 WO2006036697 A2 WO 2006036697A2
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- porous
- metal oxide
- porous metal
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- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 title claims abstract description 83
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 title claims abstract description 74
- 229910052783 alkali metal Inorganic materials 0.000 title claims abstract description 69
- 150000001340 alkali metals Chemical class 0.000 title claims abstract description 69
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 title claims abstract description 42
- 229910052751 metal Inorganic materials 0.000 claims abstract description 188
- 239000002184 metal Substances 0.000 claims abstract description 188
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 165
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 165
- 239000000203 mixture Substances 0.000 claims abstract description 111
- 239000011734 sodium Substances 0.000 claims abstract description 90
- 238000006243 chemical reaction Methods 0.000 claims abstract description 47
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 41
- 239000000956 alloy Substances 0.000 claims abstract description 41
- 229910052708 sodium Inorganic materials 0.000 claims abstract description 38
- 239000007788 liquid Substances 0.000 claims abstract description 35
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims abstract description 32
- 238000000034 method Methods 0.000 claims abstract description 29
- 150000002739 metals Chemical class 0.000 claims abstract description 19
- 238000010438 heat treatment Methods 0.000 claims abstract description 18
- 229910052700 potassium Inorganic materials 0.000 claims abstract description 16
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000011591 potassium Substances 0.000 claims abstract description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 41
- 239000011148 porous material Substances 0.000 claims description 36
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 32
- 238000006722 reduction reaction Methods 0.000 claims description 27
- 238000002156 mixing Methods 0.000 claims description 25
- 150000002894 organic compounds Chemical class 0.000 claims description 12
- 229910052792 caesium Inorganic materials 0.000 claims description 8
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 8
- 229910052701 rubidium Inorganic materials 0.000 claims description 8
- 238000006621 Wurtz reaction Methods 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 6
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 claims description 6
- 239000003960 organic solvent Substances 0.000 claims description 5
- 238000005695 dehalogenation reaction Methods 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 4
- 230000006872 improvement Effects 0.000 claims description 4
- 229910001092 metal group alloy Inorganic materials 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 239000000463 material Substances 0.000 abstract description 99
- 239000000843 powder Substances 0.000 abstract description 27
- 238000002844 melting Methods 0.000 abstract description 26
- 230000008018 melting Effects 0.000 abstract description 22
- 238000002360 preparation method Methods 0.000 abstract description 17
- 230000009467 reduction Effects 0.000 abstract description 15
- 230000001603 reducing effect Effects 0.000 abstract description 13
- 229910000573 alkali metal alloy Inorganic materials 0.000 abstract description 11
- 239000003638 chemical reducing agent Substances 0.000 abstract description 8
- 230000009257 reactivity Effects 0.000 abstract description 8
- BITYAPCSNKJESK-UHFFFAOYSA-N potassiosodium Chemical compound [Na].[K] BITYAPCSNKJESK-UHFFFAOYSA-N 0.000 abstract description 5
- 229910000799 K alloy Inorganic materials 0.000 abstract description 4
- 238000010521 absorption reaction Methods 0.000 abstract description 4
- 239000011368 organic material Substances 0.000 abstract description 3
- 239000000126 substance Substances 0.000 abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 33
- 239000001257 hydrogen Substances 0.000 description 33
- 229910052593 corundum Inorganic materials 0.000 description 24
- 229910001845 yogo sapphire Inorganic materials 0.000 description 24
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 22
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 20
- 238000000113 differential scanning calorimetry Methods 0.000 description 20
- 239000000047 product Substances 0.000 description 16
- 239000004408 titanium dioxide Substances 0.000 description 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 9
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 8
- -1 benzylic bromides Chemical class 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 229910052744 lithium Inorganic materials 0.000 description 7
- 239000000377 silicon dioxide Substances 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 239000010457 zeolite Substances 0.000 description 7
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical group C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 6
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 6
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 6
- 229940073608 benzyl chloride Drugs 0.000 description 6
- 150000005838 radical anions Chemical class 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 230000007935 neutral effect Effects 0.000 description 5
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical class [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 description 5
- 239000000741 silica gel Substances 0.000 description 5
- 229910002027 silica gel Inorganic materials 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 238000006027 Birch reduction reaction Methods 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- 230000004913 activation Effects 0.000 description 4
- 238000001994 activation Methods 0.000 description 4
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001491 aromatic compounds Chemical class 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 238000001354 calcination Methods 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 238000005859 coupling reaction Methods 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 229910003251 Na K Inorganic materials 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- 229910010062 TiCl3 Inorganic materials 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 239000012965 benzophenone Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 229910052805 deuterium Inorganic materials 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 239000002360 explosive Substances 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 239000001307 helium Substances 0.000 description 2
- 229910052734 helium Inorganic materials 0.000 description 2
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 2
- 150000004678 hydrides Chemical class 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 229910001338 liquidmetal Inorganic materials 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- 239000012808 vapor phase Substances 0.000 description 2
- 239000011592 zinc chloride Substances 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- 108091070965 Group 1 family Proteins 0.000 description 1
- 238000010541 McMurry coupling reaction Methods 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 229910009973 Ti2O3 Inorganic materials 0.000 description 1
- 229910009815 Ti3O5 Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 238000006657 acyloin condensation reaction Methods 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910000102 alkali metal hydride Inorganic materials 0.000 description 1
- 150000008046 alkali metal hydrides Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 229910002056 binary alloy Inorganic materials 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000001925 cycloalkenes Chemical class 0.000 description 1
- 238000006298 dechlorination reaction Methods 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 125000004989 dicarbonyl group Chemical group 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 230000005496 eutectics Effects 0.000 description 1
- 150000003948 formamides Chemical class 0.000 description 1
- 229910000743 fusible alloy Inorganic materials 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 238000004845 hydriding Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910001502 inorganic halide Inorganic materials 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052987 metal hydride Inorganic materials 0.000 description 1
- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229910002058 ternary alloy Inorganic materials 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- GQUJEMVIKWQAEH-UHFFFAOYSA-N titanium(III) oxide Chemical compound O=[Ti]O[Ti]=O GQUJEMVIKWQAEH-UHFFFAOYSA-N 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G23/00—Compounds of titanium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
- B01J21/04—Alumina
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
- B01J21/063—Titanium; Oxides or hydroxides thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/02—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the alkali- or alkaline earth metals or beryllium
- B01J23/04—Alkali metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0201—Impregnation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0215—Coating
- B01J37/023—Coating using molten compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/08—Heat treatment
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
- C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
- C01B3/04—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by decomposition of inorganic compounds, e.g. ammonia
- C01B3/042—Decomposition of water
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
- C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
- C01B3/06—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of inorganic compounds containing electro-positively bound hydrogen, e.g. water, acids, bases, ammonia, with inorganic reducing agents
- C01B3/065—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of inorganic compounds containing electro-positively bound hydrogen, e.g. water, acids, bases, ammonia, with inorganic reducing agents from a hydride
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
- C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
- C01B3/06—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of inorganic compounds containing electro-positively bound hydrogen, e.g. water, acids, bases, ammonia, with inorganic reducing agents
- C01B3/08—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of inorganic compounds containing electro-positively bound hydrogen, e.g. water, acids, bases, ammonia, with inorganic reducing agents with metals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/26—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only halogen atoms as hetero-atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/23—Preparation of halogenated hydrocarbons by dehalogenation
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/86—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon
- C07C2/861—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon the non-hydrocarbon contains only halogen as hetero-atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
- C07C5/321—Catalytic processes
- C07C5/324—Catalytic processes with metals
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
- B01J35/64—Pore diameter
- B01J35/647—2-50 nm
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
- B01J35/64—Pore diameter
- B01J35/651—50-500 nm
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/0081—Preparation by melting
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/16—Pore diameter
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/02—Boron or aluminium; Oxides or hydroxides thereof
- C07C2521/04—Alumina
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/02—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the alkali- or alkaline earth metals or beryllium
- C07C2523/04—Alkali metals
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
Definitions
- the invention relates to porous metal oxide compositions made by interaction of alkali metals or alloys of these metals with porous titanium oxide or porous alumina.
- the compositions have improved handling characteristics and retain the reactivity of the neutral alkali metal or alloy.
- Alkali metals those in Group 1 of the periodic table, and alloys of alkali metals, are very reactive in their metallic, or neutral, state.
- the alkali metals and their alloys are very reactive toward air and moisture and may catch fire spontaneously when exposed to these agents.
- the neutral metal or alloy must often be stored in vacuo or under an inert liquid such as oil in order to protect it from contact with the atmosphere, which may result in oxidation or other reactions.
- sodium metal is often stored in Nujol oil which must, to avoid unwanted impurities, be removed prior to use in chemical reactions. This places severe restrictions on its shipment and use.
- Lithium Catalysts J. Phys. Chem., 61, 1957, 756-758, investigated the catalytic properties of supported alkali metal catalysts for hydrogen-deuterium exchange and ethylene hydrogenation.
- Sodium dispersed on dried alumina does not increase the activity of the alumina for hydrogen-deuterium exchange.
- hydriding the sodium-alumina greatly increases the exchange activity, the hydrided catalyst being active even at -195°C.
- Sodium- silica catalysts are much less active than the corresponding sodium-alumina catalysts.
- Supported sodium and lithium catalysts are also active for ethylene hydrogenation even below room temperature; in this case, however, hydrogen treatments have relatively minor effects on the activities.
- the supported alkali metal catalysts are much more active than the bulk hydrides of sodium and lithium for both of these reactions.
- the major role of the support is probably to increase the effective area of the alkali metal.
- the results of this study suggest that the mechanisms of activation of hydrogen and ethylene on alkali metal hydrides are similar to those previously postulated for alkaline earth metal hydrides. The activations probably occur at metal sites at metal-metal hydride interfaces.
- the results obtained with the bulk hydrides suggest that hydrogen activation takes place more readily at lithium sites than at sodium sites, and the reverse situation is likely for ethylene activation. [0008] Voltz's experiment was as follows.
- the supported sodium and lithium catalysts were prepared by dispersing the molten metal over powdered alumina or silica which had been dried by evacuation at 500 0 C for about 16 hours.
- a typical preparation sodium-alumina
- the dried alumina and sodium were placed in a high vacuum reactor equipped with a magnetic stirrer. Transfers of materials to the reactor were made in a dry box in dry nitrogen. The reactor was heated lowly under evacuation while the solids were stirred. When the sodium melted, it dispersed over the alumina powder.
- the reactor was heated to about 150 0 C and kept at this temperature (under evacuation and with stirring) for at least one-half hour.
- Na/ Al 2 O 3 can be conveniently prepared in two different ways as a homogenous grey, nonpyrophoric powder (method A: mixing/grinding of Al 2 O 3 and Na at 180-190 0 C; method B: deposition of melting Na on Al 2 O 3 suspended in boiling toluene by means of an Ultra turrax stirrer). With ⁇ 4mmol Na per g of reagent (10% metal content w/w), the available surface area of the alumina is well exploited without risking any severe overloading. [0011] Furstner's experiment was as follows.
- Method A Na sand (1Og; l-2mm) was added in portions during 30 min to predried Al 2 O 3 (10Og) with good mechanical stirring under Ar at 180-190 0 C. This afforded NaZAl 2 O 3 as a grey-black, air-sensitive but nonpyrophoric powder which can be stored for extended periods of time under Ar at RT without loss of activity. According to Furstner, this simple procedure is less appropriate for the preparation of NaZTiO 2 and Na/NaCl for reasons of insufficient mixing.
- Method B To a vigorously stirred suspension of predried Al 2 O 3 (10Og) in boiling Toluene (35OmL) was added Na sand (1Og) over a period of 20 min. Stirring and reflux were continued for another 15 min, the mixture was cooled to RT, filtered under Ar, washed with pentane (ca. 30OmL in several portions) and dried in vacuo. For the preparation of NaZTiO 2 , a larger volume of toluene ( ⁇ 800mL) was required to achieve good agitation. Id. [0014] In addition, U.S. Patent Application Serial No. 10/995,327 filed November 24,
- silica gel compositions made by interaction of alkali metals or alloys of these metals with silica gel, and is hereby incorporated by reference.
- the invention relates to a Group 1 metal/porous metal oxide composition
- a Group 1 metal/porous metal oxide composition comprising the product of mixing a liquid Group 1 metal or alloy with a porous metal oxide selected from porous titanium oxide and porous alumina in an inert atmosphere under isothermal conditions near ambient temperatures sufficient to absorb the liquid Group 1 metal or alloy into the porous metal oxide pores.
- the Group 1 metal/porous metal oxide composition produced reacts with dry O 2 . This material is referred to as "Stage 0" material.
- the invention also relates to a Group 1 metal/porous metal oxide composition
- a Group 1 metal/porous metal oxide composition comprising the product of mixing a Group 1 metal or alloy with porous metal oxide selected from porous titanium oxide and porous alumina under exothermic conditions that may be above ambient temperatures sufficient to absorb the Group 1 metal or alloy into the porous metal oxide pores.
- the Group 1 metal/porous metal oxide composition produced does not react with dry O 2 . This material is referred to as "Stage I" material.
- the invention also relates to a Group 1 metal/porous metal oxide composition
- a Group 1 metal/porous metal oxide composition comprising the product of mixing a liquid Group 1 metal or alloy with porous metal oxide under conditions sufficient to absorb the liquid Group 1 metal or alloy into the porous metal oxide pores and heating the resulting mixture to a temperature of about 150 0 C or higher.
- the Group 1 metal/porous metal oxide composition produced does not react with dry O 2 .
- the invention further relates to a method for producing hydrogen gas comprising the step of contacting any of the Group 1 metal/porous metal oxide compositions described herein with water.
- the invention relates to a reduction reaction of an organic compound in the presence of an alkali metal, the improvement comprising conducting the reaction in the presence of any of the Group 1 metal/porous metal oxide compositions described herein.
- the reduction reactions may include, for example, dehalogenation reactions and Wurtz reactions.
- the invention relates to a method of drying an organic solvent comprising the step of contacting an organic solvent with porous alumina for a sufficient time to remove water from the solvent.
- the contacting step may be done by batch or through a column.
- Figure 1 shows a Differential Scanning Calorimetry (DSC) trace for a mixture of 2.9 mg of Na metal with 8.0 mg of porous Al 2 O 3 .
- Figure 2 shows a Differential Scanning Calorimetry (DSC) trace for a mixture of 3.0 mg of Na metal with 8.2 mg of porous TiO 2 .
- Figure 3 shows a Differential Scanning Calorimetry (DSC) trace for a 14.9 mg sample of Stage 0, 25 wt% Na 2 K-TiO 2 .
- Figure 4 shows a Differential Scanning Calorimetry (DSC) trace for a 6.0 mg sample of Stage I, 25 wt% Na 2 K-TiO 2 that had been heated to 150 0 C overnight.
- Figure 5 shows a Differential Scanning Calorimetry (DSC) trace for an 11.7 mg sample of Stage 0, 25 wt% Na 2 K-Al 2 O 3 , wherein the inset shows the melting endotherm of Na 2 K absorbed in the pores of the Al 2 O 3 .
- Figure 6 shows a Differential Scanning Calorimetry (DSC) trace for a 44.7 mg sample of Stage I, 21 wt% Na 2 K-Al 2 O 3 .
- Figure 7 shows the 1 H NMR spectrum of the product of reduction of benzyl chloride with Stage I, 25 wt% Na 2 K-Al 2 O 3 , wherein the major product is bibenzyl and no benzyl chloride was detected in the product.
- DETAILED DESCRIPTION OF THE INVENTION [0028] Group 1 Metals: Alkali Metals and Alkali Metal Alloys
- Alkali metals are those metals in the Group 1 family of the periodic table.
- the terms "Group 1 metal” or “Group 1 metals” are used here to describe alkali metals and alloys of alkali metals which may be used in the porous metal oxide compositions of the invention.
- Those alkali metals include sodium (Na), potassium (K), rubidium (Rb), and cesium, (Cs).
- sodium and potassium are preferred for use in the porous metal oxide compositions of the invention, with sodium being particularly preferred.
- Alkali metal alloys may also be used in the porous metal oxide compositions of the invention.
- the alkali metal alloy is preferably an alloy of two or more alkali metals, for example sodium-potassium (e.g. NaK or Na 2 K) alloys, which are particularly preferred.
- Other preferred alkali metal alloys are those containing, potassium, cesium, and rubidium with each other and particularly alloys of these elements with sodium.
- the alkali metal alloys are within the "Group 1 metal" definition as used in the specification and claims. [0031]
- the Group 1 metal is typically mixed with the porous metal oxide, porous titanium oxide or porous alumina.
- the viscosity of the liquid Group 1 metal should be at least low enough to be absorbed into the pores of the porous titanium oxide or porous alumina.
- One method to accomplish this is heating the alkali metal in an inert atmosphere prior to mixing it with the porous metal oxide.
- the Group 1 metal may be mixed as a solid with the porous metal oxide and the mixture heated to melt the alkali metal.
- Another method to introduce Group 1 metals into porous metal oxide is from the vapor phase as was done with zeolites.
- zeolites See A. S. Ichimura, J. L. Dye, M. A. Camblor and L. A. Villaescusa, J. Am. Chem. Soc, 124, 1170-1171 (2002) and D. P.Wernette, A. S. Ichimura, S. A. Urbin and J. L. Dye, Chem. Mater. 15, 1441-1448, (2003).).
- a Group 1 metal can be deposited onto the porous metal oxide from a metal- ammonia solution. (See M. Makesya and K. Grala, Syn. Lett. 1997, pp.
- the metal-ammonia solution can be used to avoid agglomeration of the metal in upon mixing with the porous metal oxide and to prepare an intimate mixture of the metal with the porous metal oxide.
- the metal-ammonia solution method of mixing Group 1 metals with porous metal oxide was accompanied by considerable decomposition of the metal-ammonia solution to form amides.
- simply allowing the liquid Group 1 metal to contact the porous metal oxide avoids the time- consuming vapor deposition or metal-ammonia routes.
- the Group 1 metal have a melting point within about 15°C of room temperature (approximately 25 0 C).
- cesium and rubidium have melting points of 28.5°C and 38.5°C, respectively.
- alloys of the two or more alkali metals are, and preferably are, liquid at or near room temperature.
- a preferred low-melting alloy is that between sodium and potassium (NaK) at various molar ratios of Na to K between 0.5 and 3.0, more preferably with a 2:1 molar ratio, i.e. Na 2 K.
- the porous metal oxide powders used in this invention are porous titanium oxides and porous alumina. Any porous titanium oxide may be used, including TiO, TiO 2 , Ti 2 O 3 , and Ti 3 O 5 . Given their porous natures, these porous metal oxides can take up large amounts of absorbed material. Unlike prior adsorption of alkali metals onto titanium oxide or alumina powders, the compositions of the invention absorb the alkali metals into the pores of porous titanium oxides and porous alumina. Porous titanium oxides and porous alumina are difference that the more familiar non-porous forms such as colloidal titanium oxides and colloidal alumina.
- Porous titanium oxides may be purchased from Sachtleben Chemie, and porous alumina may be purchased from Almatis AC.
- the porous metal oxides used in the porous metal oxide compositions of the invention preferably have pore sizes ranging from 50 A to 1000 A. More preferably, the pore size may range from 100 to 300 A. Even more preferably, the average diameter of the pores of the porous metal oxide will be approximately 150 A.
- porous metal oxides when purchased, are free-flowing powders, they typically contain large amounts of gaseous material, such as water and air. These are preferably removed prior to mixing the porous titanium oxide or porous alumina with an alkali metal or alloy to form compositions of the invention.
- the porous metal oxide may be de-gassed using methods known in the art. For example, to remove the gaseous material the porous metal oxide may be heated under vacuum in an evacuable flask, first with a hot air dryer and then with a torch. Such heating achieves temperatures of approximately 300° C.
- porous metal oxide 600 0 C or hotter (900 0 C) in air (calcination).
- the porous metal oxide is typically cooled to room temperature before preparing a Group 1 metal/porous metal oxide composition of the invention.
- the invention relates to Group 1 metal/porous metal oxide compositions comprising a porous metal oxide selected from porous titanium oxide and porous alumina and an alkali metal or an alkali metal alloy.
- the compositions of the inventions that utilize titanium oxide or porous alumina are described as Stages 0 and I materials. These materials differ in their preparation and chemical reactivity. Stage I may be prepared directly using the methods described below from an earlier preparation of Stage 0 material.
- Stage 0 materials may, for example, be prepared using liquid alloys of Na and K which are rapidly absorbed by porous titanium oxide or porous alumina under isothermal conditions, preferably at or just above room temperature, to form loose black powders that retain much of the reducing ability of the parent metals. It is believed the Stage 0 materials have small clusters of neutral Group 1 metal absorbed in the porous metal oxide pores. The Stage 0 materials are pyrophoric but less explosive in air compared to their parent Group 1 metal. Stage I materials may be prepared by heating Stage 0 materials at 150 0 C overnight. Stage I material is a loose black powder that is stable in dry air. Further heating above 200 0 C causes an exothermic reaction to produce another stage or stages.
- Preferred Group 1 metal/porous metal oxide compositions of the invention are those containing sodium, potassium, or sodium-potassium alloys with sodium and sodium-potassium alloys being most preferred.
- the Group 1 metal/ porous metal oxide compositions of the invention comprise porous metal oxide selected from porous titanium oxide and porous alumina with absorbed Group 1 metal.
- the amount of Group 1 metal loading is dependent upon the pore size and pore density of the actual porous metal oxide used.
- the Group 1 metal may be present in the compositions of the invention up to about 30 % by weight.
- the amount of metal ranges from 25 % to 30 % by weight. In the Stage I materials of the invention, loadings above about 30 % by weight result in some free metal remaining in the porous metal oxide pores or on the surface.
- the Stage 0 and Stage I metal/porous metal oxide compositions of the invention react rapidly with water to produce gaseous hydrogen.
- the yield is nearly quantitative, typically about 90-95%.
- the yield was lower.
- About 10% of the added metal did not evolve hydrogen when water was added.
- the Group 1 metal/porous metal oxide compositions of the invention whose preparation and properties are described below, show promise as easily shipped and handled sources of clean hydrogen and as powerful reducing agents for a variety of reactions of organic compounds. Table I below summarizes the preparation processes and uses of Stage 0 and I materials.
- the porous metal oxide is initially heated to approximately 600 0 C or higher in air to remove water, de-gas the porous metal oxide, and minimize defect sites. Other methods known in the art to dry, de-gas and/or passivate the porous metal oxide may also be used.
- the Stage 0 material of the invention apparently contains low-melting Group
- Stage 0 material can be viewed as nanoscale alkali metal or alkali metal alloy particles absorbed in the open pores and channels within the porous metal oxide.
- the Stage 0 material of the invention is a Group 1 metal/porous metal oxide composition comprising the product of mixing a liquid Group 1 metal or a liquid Group 1 metal alloy, such as Na 2 K, with porous titanium oxide or porous alumina under isothermal conditions sufficient to absorb the liquid Group 1 metal or liquid Group 1 metal alloy into the porous metal oxide pores.
- Preferred Group 1 metals for Stage 0 materials include a low-melting Group 1 metal such as cesium or a NaK alloy.
- the Stage 0 Group 1 metal/porous metal oxide composition of this invention reacts with dry O 2 , which differentiates it from Stage I materials. Since Stage 0 material is reactive with dry air, it should be handled in vacuo, in an oxygen-free atmosphere, and preferably in an inert atmosphere, such as under nitrogen or an inert gas. While the Stage 0 material will ignite spontaneously in air, it can be stored in a closed container, e.g. a screw-top vial.
- a Group 1 liquid metal or alloy is mixed with porous titanium oxide or porous alumina in an inert atmosphere under isothermal conditions, preferably at room temperature or slightly above, for a time sufficient to permit the alkali metal or alloy to be absorbed into the silica.
- the mixing must be done in an inert atmosphere such as within a glove box or glove bag.
- a liquid Group 1 metal such as Na 2 K, may be poured over a bed of porous metal oxide at room temperature. The mixture is agitated, preferably stirred or shaken, to achieve good mixing.
- the liquid Group 1 metal is preferably absorbed into the porous metal oxide without any significant heat of reaction or appreciable release of heat.
- the alkali metal is preferably added slowly to avoid any exothermicity due to alkali metal absorption into the pores of the porous metal oxide.
- the absorption of the liquid Group 1 metal to form Stage 0 material preferably occurs within 15°C of room temperature (25°C). In the typical process, so little heat is evolved that the sample does not become noticeably warm but converts to a product which is a free-flowing amorphous black powder, in which the individual particles have a shiny surface.
- the mixture is agitated for a time sufficient to allow the alkali metal or alloy to be absorbed or "soaked up" into the pores of the porous titanium oxide or porous alumina.
- the time of mixing generally depends upon the batch size of material being prepared and may range from several minutes to several hours. This mixing time holds true for the preparation of any Group 1 metal/porous metal oxide composition of the invention.
- Stage 0 material When preparing Stage 0 material, any heat generated by the reaction or put into the reaction should be controlled or dissipated. A significant temperature increase during the preparation should be avoided.
- the Stage 0 material is formed at ambient temperature, e.g. near room temperature (25°C). Heating much above this temperature generally leads to the formation of Stage I material.
- the temperature may be controlled by spreading the porous metal oxide (for example, on a metal tray), stirring the porous metal oxide, or by cooling the reaction vessel.
- the reaction temperature should, however, be maintained such that the Group 1 metal remains liquid so that it may be absorbed by the porous titanium oxide or porous alumina.
- Stage 0 material might slowly convert to Stage I material over time when kept at room temperature, although further conversion to higher stage material does not occur without heating as discussed below.
- the Stage 0 material is a shiny black powder that reacts exothermically with water.
- a DSC of the Stage 0 material made with alumina shows the presence of the alkali metal in its neutral state within the porous metal oxide. This endothermic melting signal was not observed with Stage 0 Group 1 metal/porous titanium oxide. While the exact composition of the Stage 0 material is not currently known, the melting point of metals within the Stage 0 material is lower than the melting point of the most common Group 1 alloys, such as Na 2 K, thus indicating that small particles of the Group 1 alloys are within the pores of the porous metal oxide.
- the Stage 0 materials are the most reactive members of the Group 1 metal/porous metal oxide compositions of the invention. Since the addition of a low-melting alkali metal or alloy to porous titanium oxide or porous alumina produces a Stage 0 material without significant heat evolution, the Stage 0 material retains most of the reducing ability of the alkali metal. Because of their reactivity toward air and moisture they must be handled with care and not allowed to come in contact with large amounts of air and moisture. In spite of these restrictions, the Stage 0 materials have utility in highly reducing chromatography applications.
- the porosity of packed columns of the Group 1 metal/porous metal oxide compositions of the invention provide a reducing environment that cannot be met with the parent metals or alloys. This, as discussed below, permits the Stage 0 material to be used to produce hydrogen from water and as a reducing agent reacting with a number of reducible organic materials in a manner similar to that of the pure alkali metals.
- the Stage I material of the invention is a Group 1 metal/porous metal oxide composition comprising the product of heating the Stage 0 material or mixing a solid Group 1 metal with porous titanium oxide or porous alumina and heating the mixture above the melting temperature of the metal in order to absorb the Group 1 metal into the porous metal oxide pores.
- the Stage I Group 1 metal/porous metal oxide composition produced does not react with dry O 2 .
- the alkali metal or alloy has been converted to a form that loses the properties of the bulk metal, such as melting.
- the Stage I material of the invention may be formed by mixing the liquid
- Group 1 metal at or just above its melting point with porous titanium oxide or porous alumina under an inert atmosphere to allow the Group 1 metal to be absorbed into the pores of the porous metal oxide.
- the Group 1 metal may also be mixed with the porous metal oxide using one of the alternative methods discussed above, such as adding the Group 1 metal as a vapor. The mixture is then maintained at or slightly above the melting point of the Group 1 metal (i.e., approximately 70 0 C to 150 0 C) and agitated for between several minutes to several hours. Generally speaking, higher reaction temperatures convert the material in shorter times.
- the reaction to form Stage I materials is mildly exothermic, and, on a large scale, the process would be preferably done by adding the liquid metal or alloy to the porous metal oxide with continual mixing, in such a way as to remove heat as it is produced.
- the reaction appears to form an alkali metal - porous metal oxide lattice.
- the exothermic nature of the reaction differentiates Stage I material from Stage 0 material. Heating above the exotherm can convert Stage I material to higher stage materials, depending upon the temperature.
- Stage I materials When low-melting Group 1 metals are added to calcined and outgassed porous metal oxide in a closed environment such as an Erlenmeyer flask, the system often becomes warm because of exothermic reactions between the alkali metal and the porous metal oxide or its defect sites. This can result in the formation of mixtures of Stages 0 and I.
- the simplest and most direct preparation of Stage I materials is to heat Stage 0 samples overnight under an inert atmosphere at temperatures of 150 0 C. Other times and temperatures may work also, but care should be taken to avoid overheating, which can lead to the formation of higher stage materials. To insure a homogeneous product, provision should be made for agitation during the heating process.
- the Stage I material is an amorphous, black powder that does not immediately react with dry air, but reacts exothermically with water.
- a DSC of the Stage I material shows little or no Group 1 metal remaining within the porous metal oxide.
- the difference between Stages I and 0 is that the former can be handled in dry air and even quickly transferred in ordinary laboratory air without catching fire or degrading rapidly.
- Stage I material in contrast to Stage 0 material, which reacts which dry O 2 ) is unchanged and produces the same amount of hydrogen gas upon reaction with liquid water as do fresh samples.
- Stage I material has many uses in reactive chemistry as an active reducing agent, and for hydrogen production. [0057] Thermal Behavior
- Group 1 metals react exothermically with the porous metal oxide compositions of the invention.
- the dashed line is a repeat scan that shows no major thermal peaks. In figure 1, the solid line represents the first scan, and the dashed line represents a repeat scan.
- FIG. 2 shows a Differential Scanning Calorimetry (DSC) trace for a similar mixture of 8.2 mg of porous titanium dioxide (TiO 2 ) and 3.0 mg of Na metal in the DSC pan.
- Figure 3 shows a Differential Scanning Calorimetry (DSC) trace for a 14.9 mg sample of Stage 0, 25 wt% Na 2 K-TiO 2 prepared according to the procedure discussed in Example 2. Note the absence of a melting endotherm and the substantial exotherms as reaction between the metal and the TiO 2 occurs.
- Figure 4 shows a Differential Scanning Calorimetry (DSC) trace for a 6.0 mg sample of Stage I, 25 wt% Na 2 K-TiO 2 that had been heated to 150 0 C overnight, as discussed in Example 2.
- Figure 5 shows a Differential Scanning Calorimetry (DSC) trace for an 11.7 mg sample of Stage 0, 25 wt% Na 2 K-Al 2 O 3 prepared according to the procedure discussed in Example 1.
- the inset shows the melting endotherm of Na 2 K absorbed in the pores of the Al 2 O 3 . Broad exotherms are also evident from 50 - 250 0 C.
- Figure 6 shows a Differential Scanning Calorimetry (DSC) trace for a 44.7 mg sample of Stage I, 21 wt% Na 2 K-Al 2 O 3 prepared according to the procedure discussed in Example 3.
- Figure 7 shows a 1 H NMR spectrum of the product of reduction (with Stage I, 25 wt% Na 2 K-Al 2 O 3 ) of benzyl chloride in d-8 tetrahydrofuran (THF) prepared according to the procedure discussed in Example 5.
- the major product is bibenzyl.
- the aromatic region is on the left and the aliphatic region is on the right.
- the major peak of bibenzyl is at 2.86 ppm.
- the small peaks to the left are from THF and the small peak at 2.27 ppm is from the minor product, toluene.
- All Group 1 metal/porous metal oxide compositions of the invention react with water exothermically to produce hydrogen.
- the compositions of the invention retain the reactivity of the Group 1 metal.
- Stage 0 material can be handled briefly in dry air, but it reacts slowly with oxygen and rapidly with moisture.
- Stage I of the Group 1 metal/porous metal oxide compositions are unreactive towards dry oxygen.
- the porous alumina yields recyclable alumina. Accordingly, the porous alumina yields an effective way to dry solvents by contacting the solvent with the porous alumina, thereby removing any water without consuming the porous alumina. This drying may be implemented either through a column or by a batch process.
- Stage I Group 1 metal/porous metal oxide compositions of the invention are relatively innocuous and not violently reactive, they do have a strong base present and form alkali metal hydroxides upon reaction with water.
- the alumina based materials of the invention form a solid white reaction product that can be recycled merely by washing with water and re-calcining at 600 0 C as shown in Example 6.
- the titanium oxide based materials of the invention form a black solid upon reaction with water.
- Each stage of the Group 1 metal/porous metal oxide composition of the invention may be used as a reducing agent reacting with a number of reducible organic materials in the same manner known for alkali metals and their alloys.
- the Group 1 metal/porous metal oxide compositions may be used to reduce aromatic compounds to their radical anions as is common in the so-called Birch reductions, commonly carried out with alkali metal - ammonia solutions.
- Birch reduction is a general method of reduction of aromatic compounds by alkali metals in liquid ammonia. The theoretical and preparative aspects of the Birch reduction have been discussed in several reviews. ⁇ See, G. W. Watt, Chem. Rev., 46, 317 (1950); A. J.
- the Group 1 metal/porous metal oxide compositions of the invention readily form aromatic radical anions with both naphthalene and anthracene in tetrahydrofuran (THF) solutions. Thus, they could be substituted for the sodium in Birch reductions.
- Example 4 shows a reduction reaction that uses a Group 1 metal/porous metal oxide composition of the invention.
- the Wurtz reaction is the coupling of two organic radicals (R) by treating two moles of the organic halides (RX) with two moles of sodium:
- Use of the Group 1 metal/porous metal oxide compositions of the invention allow alkali metal reactions such as those described above to be carried out under safer conditions due to the safer handling of the compositions over the corresponding alkali metal or alloy. Use of the compositions also generally gives higher yields than the corresponding reaction with just the Group 1 metal.
- Stage I material such as a Stage I Na 2 K/porous metal oxide composition
- Stage I material is very easy to prepare and retains much of the reducing ability of the parent Group 1 metal, it is likely to find use as a powerful and convenient reducing agent.
- Small glass columns filled with the Stage I powder are able to reduce a variety of organic compounds when they are dissolved in tetrahydrofuran (THF) and passed through the column.
- batch reactions can be carried out simply by stirring THF solutions of the organic compounds with the Stage I material. For example, as is shown below, benzophenone (1) is reduced to the radical anion (ketyl); and benzyl chloride (2) undergoes Wurtz reduction to form bibenzyl (3).
- Stage I materials can reduce naphthalene to the radical anion and can convert benzyl chloride (2) to bibenzyl (3).
- the reduction of the representative compounds discussed above indicate that the Group 1 metal/porous metal oxide compositions of the invention can reduce aromatic compounds to the radical anions or dianions and completely dechlorinate aromatic chlorides. This material might therefore be able to destroy PCB 's by dechlorination.
- the powerful reducing properties of the Group 1 metal/ porous metal oxide compositions of the invention also permit the use of chromatographic columns packed with this material for the reduction of organic and inorganic compounds that are now reduced by Na-K or alkali metal-ammonia solutions.
- a major use for both stages of reduced porous metal oxide compositions of the invention is in the fuel storage potential and the formation of hydrogen gas needed for mobile fuel cells.
- large stocks of the reduced porous metal oxide powder might be kept on conveyor trays within a holding tank. Addition to water would liberate pure hydrogen gas plus water vapor.
- Both stages of reduced porous alumina produce near quantitative amounts of the hydrogen that would have been produced from the alkali metal used. The hydrogen could then be used to power mobile fuel cells.
- stocks of the Group 1 metal/porous metal oxide compositions might be kept on conveyer trays within a holding tank. Water is then introduced and the mixing with the water would liberate hydrogen which can then be extracted and compressed or pressurized. The compressed hydrogen would be used to fill mobile fuel cells.
- the spent powder, at this stage is now just porous metal oxide that could be reactivated with new Group 1 metal or used for other purposes.
- Example 1 Exemplary porous metal oxides. Porous TiO 2 (Anatase) from
- Example 2 One significant feature of the Group 1 metal/porous metal oxide compositions of the invention is their ability to produce pure hydrogen gas upon addition to water.
- the "reducing power" of the Group 1 metal/porous metal oxide compositions was determined by adding water to an evacuated sample and collecting hydrogen with a modified Toeppler pump. The reducing power is defined as the weight percent of alkali metal or alloy used that would produce the same amount of hydrogen. This was verified by collecting the hydrogen produced from a known mass of material upon reaction with out-gassed water. The hydrogen was collected in a calibrated pipette using a modified Toeppler pump (mercury filled). Such analyses were run on every sample of reduced porous metal oxide, regardless of the stage of the material.
- the amount of hydrogen produced was generally within 90 - 95% of the amount that would have been produced by the metal(s) alone.
- the amount of hydrogen was reduced by an amount equivalent to about 10% metal.
- a Stage 0 sample that was prepared with 25 wt% Na 2 K yielded hydrogen equivalent to only 13 wt% metal and another sample with 12 wt% metal yielded hydrogen equivalent to only 3 wt% Na 2 K, as shown in Figure 3.
- a sample of Stage I Na-TiO 2 made with 25 wt% Na yielded hydrogen equivalent to only 16 wt% metal.
- Example 3 The preparation of Stage I material can be performed by continuous heating of Stage 0 materials to 150 0 C or by using the higher melting alkali metals, such as sodium and potassium.
- Outgassed and calcined porous alumina 14.0 g was weighed out and, together with 6.0 g of Na metal, was introduced into a Parr Stainless steel reactor equipped with a Teflon gasket seal.
- the combination of porous metal oxide and Na was heated while rotating the reactor end-over-end at 60 rpm, first to 105 0 C for 1 hr, then overnight at 155 0 C.
- the powder was loose, black and free flowing.
- Similar processes to convert Stage 0 Na 2 K-Al 2 O 3 , Na 2 K-TiO 2 and Na-TiO 2 to Stage I materials were also carried out. For example, a DSC of 21 wt% material is shown in Figure 6.
- Example 4 All of the alkali metal-porous metal oxide powders, whether
- Stage 0 or Stage I are able to reduce naphthalene and anthracene to the corresponding radical anions
- the reduction was observed by the formation of an intense green or blue color of the solutions, respectively.
- These radical anions are stable enough to persist in solution for many hours.
- This reaction can be performed using several reaction setups, such as a batch reaction, or a chromatographic column loaded with the reducing material of the invention.
- the reaction with anthracene may be illustrated as is shown below.
- Example 5 One of the earliest reactions of alkali metals with organic compounds is the Wurtz reaction in which de-halogenation of a chlorocarbon results in coupling to form a new carbon-carbon bond. When used with a bulk alkali metal and the neat chlorocarbon however, the reaction can be dangerously explosive. As is shown below, this coupling reaction was carried out with benzyl chloride dissolved in THF by reduction with both Stage I Na 2 K-TiO 2 and Stage I Na 2 K-Al 2 O 3 (-25 wt% Na 2 K). The former was done by passage though a small column made from a Pasteur pipet and filled with the reducing material and the latter was done in a batch reaction. The only product detected by 1 H NMR was bibenzyl (See Figure 7)
- Example 6 To check the ability to recycle Stage I Na 2 K-Al 2 O 3 , about 7.5 g of this material was reacted with water, resulting in the formation of copious amounts of a white residue. This was washed five times (with centrifugation each time) and dried. The dried powder was then calcined at 600 0 C and brought into the helium-filled glove box. The recovered sample weighed 5.0 g and was combined drop-wise with 1.86 g of Na 2 K to form a loose black powder with a nominal metal concentration of 27.3 wt%. Hydrogen collection from this re-constituted Na 2 K-Al 2 O 3 yielded hydrogen equivalent to 20.8 wt % metal.
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Abstract
The invention relates to Group 1 metal/porous metal oxide compositions comprising porous metal oxide selected from porous titanium oxide and porous alumina and an alkali metal or an alkali metal alloy. The compositions of the inventions are described as Stage 0 and I materials. These materials differ in their preparation and chemical reactivity. Each successive stage may be prepared directly using the methods described below or from an earlier stage material. Stage 0 materials may, for example, be prepared using liquid alloys of Na and K which are rapidly absorbed by porous metal oxide under isothermal conditions, preferably at or just above room temperature, to form loose black powders that retain much of the reducing ability of the parent metals. When the low melting Group 1 metals are absorbed into the porous metal oxide at about 150°C, an exothermic reaction produces Stage I material, loose black powders that are stable in dry air. Further heating forms higher stage materials of unknown composition. It is believed that Stage I higher materials represent reductions of the porous metal oxide after absorption of the Group 1 metal. Preferred Group 1 metal/porous metal oxide compositions of the invention are those containing sodium, potassium, or sodium-potassium alloys with sodium and sodium-potassium alloys being most preferred. Each stage of the Group 1 metal/porous metal oxide composition of the invention may be used as a reducing agent reacting with a number of reducible organic materials in the same manner known for alkali metals and their alloys.
Description
TITANIUM OXIDE AND ALUMINA ALKALI METAL COMPOSITIONS
FIELD OF THE INVENTION
[0001] The invention relates to porous metal oxide compositions made by interaction of alkali metals or alloys of these metals with porous titanium oxide or porous alumina. The compositions have improved handling characteristics and retain the reactivity of the neutral alkali metal or alloy.
BACKGROUND OF THE INVENTION
[0002] Alkali metals, those in Group 1 of the periodic table, and alloys of alkali metals, are very reactive in their metallic, or neutral, state. The alkali metals and their alloys are very reactive toward air and moisture and may catch fire spontaneously when exposed to these agents. To avoid the inherent hazards associated with their activity, the neutral metal or alloy must often be stored in vacuo or under an inert liquid such as oil in order to protect it from contact with the atmosphere, which may result in oxidation or other reactions. For example, sodium metal is often stored in Nujol oil which must, to avoid unwanted impurities, be removed prior to use in chemical reactions. This places severe restrictions on its shipment and use.
[0003] The combination of alkali metals with silica zeolites, such as ZSM-5, has been extensively studied in many laboratories. For example, it was recently shown that pure silica zeolites can absorb up to 12 mole percent cesium from the vapor phase and comparable amounts of the other alkali metals (except lithium). Prior research with alkali metal encapsulation in all-silica zeolites revealed that such a combination reacts exothermically with water to produce hydrogen quantitatively. (See, for example, "Toward Inorganic Electrides", A. S. Ichimura, J. L. Dye, M. A. Camblor and L. A. Villaescusa, J. Am. Chem. Soc, 124, 1170-1171 (2002) and "Inorganic Electrides Formed by Alkali Metal Addition to Pure Silica Zeolites", D. P.Wernette, A. S. Ichimura, S. A. Urbin and J. L. Dye, Chem. Mater. 15, 1441-1448, (2003). The concentration of sodium absorbed by the zeolite compositions, however, was too low to be practical. In addition, the reaction was relatively slow with slow sodium diffusion within the limited zeolite pore size. [0004] The use of potassium metal dispersed on silica as a reagent in organic synthesis has been reported by Levy et al, Angew. Chem. Int. Ed. Engl. 20 (1981) p. 1033. Potassium metal was dispersed onto silica gel (CAS Registry No. 7631-86-9: actually colloidal silica, which has no internal surface area) producing an amorphous material. The
reactivity of the material was demonstrated with water and benzophenone, as shown below. See also, Russel, et al., Organometallics 2002, 21, 4113-4128, Scheme 3. [0005] It has been reported to disperse sodium on titanium dioxide (TiO2) to readily reduce zinc chloride leading to a highly active zinc powder which inserts into secondary alklyl and benzylic bromides under mild conditions, producing the corresponding zinc reagents in high yield. (See Heinz Stadtmuller, Bjorn Greve, Klaus Lennick, Abdelatif Chair, and Paul Knochel, "Preparation of Secondary Alkyl and Benzylic Zinc Bromides Using Activated Zinc Metal Deposited on Titanium Dioxide" Syntheis, 1995, 69-72.). According to Stadtmuller, it was observed that residual water content in the support has a detrimental effect. For this reason, solid supports like barium, tin, or alumina, as well as silica, could not be used. Commercial TiO2 is almost water free and constitutes the best support for this purpose. Thus the addition of sodium (ca. 8g/100g TiO2) to TiO2 (dried at 1500C for 2 hrs) at 1500C, produces a homogenous, gray powder after 15 min. This powder is not pyrophoric but its exposure to air and moisture results in a slow decomposition (2-3min). Na ™2(.50-c,2/,,o , Na t ΉO^ zπeyo-cismiimmF) ) Zn , Ti0^
[0006] Stadtmuller' s experiment was as follows. A 3-necked 100 mL flask equipped with Ar inlet, a glass stopper, and a septum cap was charged with TiO2 (18g, 380mmol) and heated for 2 hr at 1500C under vacuum (0.1 mmHg). The glass stopper was replaced with a mechanical stirrer, the reaction flask was flushed with Ar and Na (1.5Og, 65mmol) was added at once. Alternatively, the Na could be added at 25°C to the dry TiO2. The reaction mixture was vigorously stirred at 1500C for 15 min and cooled to 00C leading to a gray homogenous powder. A solution of dry ZnCl2 (4.57g, 35.5mmol) in THF (2OmL) was added with stirring. After 15 min., the activated Zn on TiO2 was ready to use.
[0007] Sterling E. Voltz, in "The Catalytic Properties of Supported Sodium and
Lithium Catalysts" J. Phys. Chem., 61, 1957, 756-758, investigated the catalytic properties of supported alkali metal catalysts for hydrogen-deuterium exchange and ethylene hydrogenation. Sodium dispersed on dried alumina does not increase the activity of the alumina for hydrogen-deuterium exchange. However, hydriding the sodium-alumina greatly increases the exchange activity, the hydrided catalyst being active even at -195°C. Sodium- silica catalysts are much less active than the corresponding sodium-alumina catalysts. Supported sodium and lithium catalysts are also active for ethylene hydrogenation even below room temperature; in this case, however, hydrogen treatments have relatively minor effects on the activities. The supported alkali metal catalysts are much more active than the
bulk hydrides of sodium and lithium for both of these reactions. The major role of the support is probably to increase the effective area of the alkali metal. The results of this study suggest that the mechanisms of activation of hydrogen and ethylene on alkali metal hydrides are similar to those previously postulated for alkaline earth metal hydrides. The activations probably occur at metal sites at metal-metal hydride interfaces. The results obtained with the bulk hydrides suggest that hydrogen activation takes place more readily at lithium sites than at sodium sites, and the reverse situation is likely for ethylene activation. [0008] Voltz's experiment was as follows. The supported sodium and lithium catalysts were prepared by dispersing the molten metal over powdered alumina or silica which had been dried by evacuation at 5000C for about 16 hours. In a typical preparation (sodium-alumina) the dried alumina and sodium were placed in a high vacuum reactor equipped with a magnetic stirrer. Transfers of materials to the reactor were made in a dry box in dry nitrogen. The reactor was heated lowly under evacuation while the solids were stirred. When the sodium melted, it dispersed over the alumina powder. The reactor was heated to about 1500C and kept at this temperature (under evacuation and with stirring) for at least one-half hour. Small amounts of gaseous products were given off in some preparations when the molten alkali metal dispersed over the powder. In the preparation of lithium- alumina catalysts, the reactor was heated to about 2800C because of the higher melting point of lithium (186°C).
[0009] Morevoer, Alois Furstner and Gunter Seidel, in " 'High-Surface Sodium' as a
Reducing Agent for TiCl3" Synthesis, 1995, 63-68., disclosed that sodium deposited on inorganic supports such as Al2O3, TiO2, and NaCl ('high-surface sodium') is a cheap, readily prepared, nonpyrophoric reducing agent for TiCl3. The low-valent Ti thus obtained, after only 1 hr. reduction time, is well suited for McMurry coupling reactions, particularly of aromatic carbonyl compounds. It exhibits a previously unrivalled template effect for the cyclization of dicarbonyl compounds to (macrocyclic) cycloalkenes and is suitable for the reduction of N-acyl-2-aminobenzophenone derivatives to 2,3-disubstituted indoles. [0010] In this regard, Na/ Al2O3 can be conveniently prepared in two different ways as a homogenous grey, nonpyrophoric powder (method A: mixing/grinding of Al2O3 and Na at 180-1900C; method B: deposition of melting Na on Al2O3 suspended in boiling toluene by means of an Ultra turrax stirrer). With ~4mmol Na per g of reagent (10% metal content w/w), the available surface area of the alumina is well exploited without risking any severe overloading.
[0011] Furstner's experiment was as follows.
[0012] Method A: Na sand (1Og; l-2mm) was added in portions during 30 min to predried Al2O3 (10Og) with good mechanical stirring under Ar at 180-1900C. This afforded NaZAl2O3 as a grey-black, air-sensitive but nonpyrophoric powder which can be stored for extended periods of time under Ar at RT without loss of activity. According to Furstner, this simple procedure is less appropriate for the preparation of NaZTiO2 and Na/NaCl for reasons of insufficient mixing.
[0013] Method B: To a vigorously stirred suspension of predried Al2O3 (10Og) in boiling Toluene (35OmL) was added Na sand (1Og) over a period of 20 min. Stirring and reflux were continued for another 15 min, the mixture was cooled to RT, filtered under Ar, washed with pentane (ca. 30OmL in several portions) and dried in vacuo. For the preparation of NaZTiO2, a larger volume of toluene (~800mL) was required to achieve good agitation. Id. [0014] In addition, U.S. Patent Application Serial No. 10/995,327 filed November 24,
2004 and entitled "SILICA GEL COMPOSITIONS CONTAINING ALKALI METALS AND ALKALI METAL ALLOYS" describes silica gel compositions made by interaction of alkali metals or alloys of these metals with silica gel, and is hereby incorporated by reference. [0015] A need exists, therefore, to have alkali metals and their alloys available in a form that may be easily handled without a significant loss in metal reactivity. This invention answers that need.
SUMMARY OF THE INVENTION
[0016] The invention relates to a Group 1 metal/porous metal oxide composition comprising the product of mixing a liquid Group 1 metal or alloy with a porous metal oxide selected from porous titanium oxide and porous alumina in an inert atmosphere under isothermal conditions near ambient temperatures sufficient to absorb the liquid Group 1 metal or alloy into the porous metal oxide pores. The Group 1 metal/porous metal oxide composition produced reacts with dry O2. This material is referred to as "Stage 0" material. [0017] The invention also relates to a Group 1 metal/porous metal oxide composition comprising the product of mixing a Group 1 metal or alloy with porous metal oxide selected from porous titanium oxide and porous alumina under exothermic conditions that may be above ambient temperatures sufficient to absorb the Group 1 metal or alloy into the porous metal oxide pores. The Group 1 metal/porous metal oxide composition produced does not react with dry O2. This material is referred to as "Stage I" material.
[0018] The invention also relates to a Group 1 metal/porous metal oxide composition comprising the product of mixing a liquid Group 1 metal or alloy with porous metal oxide under conditions sufficient to absorb the liquid Group 1 metal or alloy into the porous metal oxide pores and heating the resulting mixture to a temperature of about 150 0C or higher. The Group 1 metal/porous metal oxide composition produced does not react with dry O2. [0019] The invention further relates to a method for producing hydrogen gas comprising the step of contacting any of the Group 1 metal/porous metal oxide compositions described herein with water. Also, the invention relates to a reduction reaction of an organic compound in the presence of an alkali metal, the improvement comprising conducting the reaction in the presence of any of the Group 1 metal/porous metal oxide compositions described herein. The reduction reactions may include, for example, dehalogenation reactions and Wurtz reactions.
[0020] In addition, the invention relates to a method of drying an organic solvent comprising the step of contacting an organic solvent with porous alumina for a sufficient time to remove water from the solvent. The contacting step may be done by batch or through a column.
BRIEF DESCRIPTION OF THE DRAWINGS
[0021] Figure 1 shows a Differential Scanning Calorimetry (DSC) trace for a mixture of 2.9 mg of Na metal with 8.0 mg of porous Al2O3.
[0022] Figure 2 shows a Differential Scanning Calorimetry (DSC) trace for a mixture of 3.0 mg of Na metal with 8.2 mg of porous TiO2.
[0023] Figure 3 shows a Differential Scanning Calorimetry (DSC) trace for a 14.9 mg sample of Stage 0, 25 wt% Na2K-TiO2.
[0024] Figure 4 shows a Differential Scanning Calorimetry (DSC) trace for a 6.0 mg sample of Stage I, 25 wt% Na2K-TiO2 that had been heated to 150 0C overnight. [0025] Figure 5 shows a Differential Scanning Calorimetry (DSC) trace for an 11.7 mg sample of Stage 0, 25 wt% Na2K-Al2O3, wherein the inset shows the melting endotherm of Na2K absorbed in the pores of the Al2O3.
[0026] Figure 6 shows a Differential Scanning Calorimetry (DSC) trace for a 44.7 mg sample of Stage I, 21 wt% Na2K-Al2O3.
[0027] Figure 7 shows the 1H NMR spectrum of the product of reduction of benzyl chloride with Stage I, 25 wt% Na2K-Al2O3, wherein the major product is bibenzyl and no benzyl chloride was detected in the product.
DETAILED DESCRIPTION OF THE INVENTION [0028] Group 1 Metals: Alkali Metals and Alkali Metal Alloys
[0029] Alkali metals are those metals in the Group 1 family of the periodic table. The terms "Group 1 metal" or "Group 1 metals" are used here to describe alkali metals and alloys of alkali metals which may be used in the porous metal oxide compositions of the invention. Those alkali metals include sodium (Na), potassium (K), rubidium (Rb), and cesium, (Cs). Of these alkali metals, sodium and potassium are preferred for use in the porous metal oxide compositions of the invention, with sodium being particularly preferred. [0030] Alkali metal alloys may also be used in the porous metal oxide compositions of the invention. The alkali metal alloy is preferably an alloy of two or more alkali metals, for example sodium-potassium (e.g. NaK or Na2K) alloys, which are particularly preferred. Other preferred alkali metal alloys are those containing, potassium, cesium, and rubidium with each other and particularly alloys of these elements with sodium. The alkali metal alloys are within the "Group 1 metal" definition as used in the specification and claims. [0031] In preparing the Group 1 metal/porous metal oxide compositions of the invention, the Group 1 metal is typically mixed with the porous metal oxide, porous titanium oxide or porous alumina. The viscosity of the liquid Group 1 metal should be at least low enough to be absorbed into the pores of the porous titanium oxide or porous alumina. One method to accomplish this is heating the alkali metal in an inert atmosphere prior to mixing it with the porous metal oxide. Alternatively, depending on the stage of material to be prepared, the Group 1 metal may be mixed as a solid with the porous metal oxide and the mixture heated to melt the alkali metal.
[0032] Another method to introduce Group 1 metals into porous metal oxide is from the vapor phase as was done with zeolites. (See A. S. Ichimura, J. L. Dye, M. A. Camblor and L. A. Villaescusa, J. Am. Chem. Soc, 124, 1170-1171 (2002) and D. P.Wernette, A. S. Ichimura, S. A. Urbin and J. L. Dye, Chem. Mater. 15, 1441-1448, (2003).). In another method, a Group 1 metal can be deposited onto the porous metal oxide from a metal- ammonia solution. (See M. Makesya and K. Grala, Syn. Lett. 1997, pp. 267-268, "Convenient Preparation of 'High Surface Sodium' in Liquid Ammonia: Use in Acyloin Reaction."). The metal-ammonia solution can be used to avoid agglomeration of the metal in upon mixing with the porous metal oxide and to prepare an intimate mixture of the metal with the porous metal oxide. However, in practice the metal-ammonia solution method of mixing Group 1 metals with porous metal oxide was accompanied by considerable decomposition of
the metal-ammonia solution to form amides. However, as preferred for the invention, simply allowing the liquid Group 1 metal to contact the porous metal oxide avoids the time- consuming vapor deposition or metal-ammonia routes.
[0033] As discussed below, for at least Stage 0 material, it is generally preferred that the Group 1 metal have a melting point within about 15°C of room temperature (approximately 250C). For example cesium and rubidium have melting points of 28.5°C and 38.5°C, respectively. Typically alloys of the two or more alkali metals are, and preferably are, liquid at or near room temperature. A preferred low-melting alloy is that between sodium and potassium (NaK) at various molar ratios of Na to K between 0.5 and 3.0, more preferably with a 2:1 molar ratio, i.e. Na2K. All Na-K alloys with mole ratios between 0.5 and 2.5 begin melting at a eutectic melting temperature of -12.6°C. Melting is complete at 25°C for mole ratios of about 0.12 and 3.1. Other binary alloys of the alkali metals, such as Cs with Rb, K, or Na and Rb with Na or K also melt below, or only slightly above room temperature and would therefore be appropriate to use for this purpose. Ternary alloys, made from three of these four alkali metals, or an alloy of all four would also melt at low enough temperatures to form a Group 1 metal/porous metal oxide composition of the invention. [0034] Porous Metal Oxides
[0035] The porous metal oxide powders used in this invention are porous titanium oxides and porous alumina. Any porous titanium oxide may be used, including TiO, TiO2, Ti2O3, and Ti3O5. Given their porous natures, these porous metal oxides can take up large amounts of absorbed material. Unlike prior adsorption of alkali metals onto titanium oxide or alumina powders, the compositions of the invention absorb the alkali metals into the pores of porous titanium oxides and porous alumina. Porous titanium oxides and porous alumina are difference that the more familiar non-porous forms such as colloidal titanium oxides and colloidal alumina. Porous titanium oxides may be purchased from Sachtleben Chemie, and porous alumina may be purchased from Almatis AC. [0036] The porous metal oxides used in the porous metal oxide compositions of the invention preferably have pore sizes ranging from 50 A to 1000 A. More preferably, the pore size may range from 100 to 300 A. Even more preferably, the average diameter of the pores of the porous metal oxide will be approximately 150 A.
[0037] Although porous metal oxides, when purchased, are free-flowing powders, they typically contain large amounts of gaseous material, such as water and air. These are preferably removed prior to mixing the porous titanium oxide or porous alumina with an alkali metal or alloy to form compositions of the invention. The porous metal oxide may be
de-gassed using methods known in the art. For example, to remove the gaseous material the porous metal oxide may be heated under vacuum in an evacuable flask, first with a hot air dryer and then with a torch. Such heating achieves temperatures of approximately 300° C. It is also possible, and is actually preferred, to remove the gases more easily and to passivate active sites by heating the porous metal oxide to 6000C or hotter (9000C) in air (calcination). The porous metal oxide is typically cooled to room temperature before preparing a Group 1 metal/porous metal oxide composition of the invention.
[0038] Porous Metal Oxide Compositions Containing Alkali Metal and Alkali Metal
Alloys
[0039] The ability to utilize alkali metals or their equivalents in a convenient form continues to be a need in the chemical industry and for the hydrogen production community. Answering that need, the invention relates to Group 1 metal/porous metal oxide compositions comprising a porous metal oxide selected from porous titanium oxide and porous alumina and an alkali metal or an alkali metal alloy. The compositions of the inventions that utilize titanium oxide or porous alumina are described as Stages 0 and I materials. These materials differ in their preparation and chemical reactivity. Stage I may be prepared directly using the methods described below from an earlier preparation of Stage 0 material. Stage 0 materials may, for example, be prepared using liquid alloys of Na and K which are rapidly absorbed by porous titanium oxide or porous alumina under isothermal conditions, preferably at or just above room temperature, to form loose black powders that retain much of the reducing ability of the parent metals. It is believed the Stage 0 materials have small clusters of neutral Group 1 metal absorbed in the porous metal oxide pores. The Stage 0 materials are pyrophoric but less explosive in air compared to their parent Group 1 metal. Stage I materials may be prepared by heating Stage 0 materials at 1500C overnight. Stage I material is a loose black powder that is stable in dry air. Further heating above 200 0C causes an exothermic reaction to produce another stage or stages. It is believed that Stage I and the materials formed at higher temperatures represent reductions of the porous metal oxide after absorption of the Group 1 metal. Preferred Group 1 metal/porous metal oxide compositions of the invention are those containing sodium, potassium, or sodium-potassium alloys with sodium and sodium-potassium alloys being most preferred.
[0040] As described below, a number of samples of this material with Na2K, at various loads and mass ratios, were tested by Differential Scanning Calorimetry (DSC). The heat absorbed upon melting Na2K in the porous metal oxide pores at -25 - 0 0C was used to determine the amount of encapsulated metal that remained as metal in the porous metal
oxide. This was followed by broad exothermic peaks between 5°C and 450 0C. Upon cooling and reheating the same sample, no appreciable thermal peaks were observed. This shows that the heat treatment causes encapsulated metal in the pores to react with porous metal oxide to produce new materials, although the boundaries are not sharp. This conversion does not appreciably change the hydrogen producing abilities of the material.
[0041] The Group 1 metal/ porous metal oxide compositions of the invention comprise porous metal oxide selected from porous titanium oxide and porous alumina with absorbed Group 1 metal. The amount of Group 1 metal loading is dependent upon the pore size and pore density of the actual porous metal oxide used. Typically, the Group 1 metal may be present in the compositions of the invention up to about 30 % by weight. Preferably, the amount of metal ranges from 25 % to 30 % by weight. In the Stage I materials of the invention, loadings above about 30 % by weight result in some free metal remaining in the porous metal oxide pores or on the surface.
[0042] The Stage 0 and Stage I metal/porous metal oxide compositions of the invention react rapidly with water to produce gaseous hydrogen. In the case of Stage I metal/porous alumina the yield is nearly quantitative, typically about 90-95%. However in the case of Stage 0 and Stage I metal/porous titanium oxide, the yield was lower. About 10% of the added metal did not evolve hydrogen when water was added. Apparently the metal reacted with the porous titanium oxide to produce a product that did not react with water to produce hydrogen. The Group 1 metal/porous metal oxide compositions of the invention, whose preparation and properties are described below, show promise as easily shipped and handled sources of clean hydrogen and as powerful reducing agents for a variety of reactions of organic compounds. Table I below summarizes the preparation processes and uses of Stage 0 and I materials.
Table I Summary of Stages 0 and I
[0043] As discussed above, to prepare all of the Group 1 metal/porous metal oxide compositions of the invention, it is preferred to de-gas and passivate the porous titanium oxide or porous alumina prior to mixing it with the Group 1 metal. Typically, in preparing the materials of the invention, the porous metal oxide is initially heated to approximately 6000C or higher in air to remove water, de-gas the porous metal oxide, and minimize defect sites. Other methods known in the art to dry, de-gas and/or passivate the porous metal oxide may also be used. [0044] Stage 0 Material
[0045] The Stage 0 material of the invention apparently contains low-melting Group
1 metals absorbed into the pores of porous metal oxide without reaction (except for the partial reaction with porous titanium oxide described above). Thus, Stage 0 material can be viewed as nanoscale alkali metal or alkali metal alloy particles absorbed in the open pores and channels within the porous metal oxide. The Stage 0 material of the invention is a Group 1 metal/porous metal oxide composition comprising the product of mixing a liquid Group 1 metal or a liquid Group 1 metal alloy, such as Na2K, with porous titanium oxide or porous alumina under isothermal conditions sufficient to absorb the liquid Group 1 metal or liquid
Group 1 metal alloy into the porous metal oxide pores. Preferred Group 1 metals for Stage 0 materials include a low-melting Group 1 metal such as cesium or a NaK alloy. The Stage 0 Group 1 metal/porous metal oxide composition of this invention reacts with dry O2, which differentiates it from Stage I materials. Since Stage 0 material is reactive with dry air, it should be handled in vacuo, in an oxygen-free atmosphere, and preferably in an inert atmosphere, such as under nitrogen or an inert gas. While the Stage 0 material will ignite spontaneously in air, it can be stored in a closed container, e.g. a screw-top vial. [0046] To form Stage 0 materials, a Group 1 liquid metal or alloy is mixed with porous titanium oxide or porous alumina in an inert atmosphere under isothermal conditions, preferably at room temperature or slightly above, for a time sufficient to permit the alkali metal or alloy to be absorbed into the silica. The mixing must be done in an inert atmosphere such as within a glove box or glove bag. During formation of a preferred Stage 0 material, a liquid Group 1 metal, such as Na2K, may be poured over a bed of porous metal oxide at room temperature. The mixture is agitated, preferably stirred or shaken, to achieve good mixing. The liquid Group 1 metal is preferably absorbed into the porous metal oxide without any significant heat of reaction or appreciable release of heat. At larger scales, the alkali metal is preferably added slowly to avoid any exothermicity due to alkali metal absorption into the pores of the porous metal oxide.
[0047] Depending upon the Group 1 metal used, the absorption of the liquid Group 1 metal to form Stage 0 material preferably occurs within 15°C of room temperature (25°C). In the typical process, so little heat is evolved that the sample does not become noticeably warm but converts to a product which is a free-flowing amorphous black powder, in which the individual particles have a shiny surface. The mixture is agitated for a time sufficient to allow the alkali metal or alloy to be absorbed or "soaked up" into the pores of the porous titanium oxide or porous alumina. The time of mixing generally depends upon the batch size of material being prepared and may range from several minutes to several hours. This mixing time holds true for the preparation of any Group 1 metal/porous metal oxide composition of the invention.
[0048] When preparing Stage 0 material, any heat generated by the reaction or put into the reaction should be controlled or dissipated. A significant temperature increase during the preparation should be avoided. In a preferred embodiment, the Stage 0 material is formed at ambient temperature, e.g. near room temperature (25°C). Heating much above this temperature generally leads to the formation of Stage I material. The temperature may be controlled by spreading the porous metal oxide (for example, on a metal tray), stirring the
porous metal oxide, or by cooling the reaction vessel. The reaction temperature should, however, be maintained such that the Group 1 metal remains liquid so that it may be absorbed by the porous titanium oxide or porous alumina. It should also be noted that Stage 0 material might slowly convert to Stage I material over time when kept at room temperature, although further conversion to higher stage material does not occur without heating as discussed below.
[0049] The Stage 0 material is a shiny black powder that reacts exothermically with water. A DSC of the Stage 0 material made with alumina shows the presence of the alkali metal in its neutral state within the porous metal oxide. This endothermic melting signal was not observed with Stage 0 Group 1 metal/porous titanium oxide. While the exact composition of the Stage 0 material is not currently known, the melting point of metals within the Stage 0 material is lower than the melting point of the most common Group 1 alloys, such as Na2K, thus indicating that small particles of the Group 1 alloys are within the pores of the porous metal oxide.
[0050] The Stage 0 materials are the most reactive members of the Group 1 metal/porous metal oxide compositions of the invention. Since the addition of a low-melting alkali metal or alloy to porous titanium oxide or porous alumina produces a Stage 0 material without significant heat evolution, the Stage 0 material retains most of the reducing ability of the alkali metal. Because of their reactivity toward air and moisture they must be handled with care and not allowed to come in contact with large amounts of air and moisture. In spite of these restrictions, the Stage 0 materials have utility in highly reducing chromatography applications. The porosity of packed columns of the Group 1 metal/porous metal oxide compositions of the invention provide a reducing environment that cannot be met with the parent metals or alloys. This, as discussed below, permits the Stage 0 material to be used to produce hydrogen from water and as a reducing agent reacting with a number of reducible organic materials in a manner similar to that of the pure alkali metals. [0051] Stage I Material
[0052] The Stage I material of the invention is a Group 1 metal/porous metal oxide composition comprising the product of heating the Stage 0 material or mixing a solid Group 1 metal with porous titanium oxide or porous alumina and heating the mixture above the melting temperature of the metal in order to absorb the Group 1 metal into the porous metal oxide pores. The Stage I Group 1 metal/porous metal oxide composition produced does not react with dry O2. In the Stage I material it appears that the alkali metal or alloy has been converted to a form that loses the properties of the bulk metal, such as melting.
[0053] The Stage I material of the invention may be formed by mixing the liquid
Group 1 metal, at or just above its melting point with porous titanium oxide or porous alumina under an inert atmosphere to allow the Group 1 metal to be absorbed into the pores of the porous metal oxide. The Group 1 metal may also be mixed with the porous metal oxide using one of the alternative methods discussed above, such as adding the Group 1 metal as a vapor. The mixture is then maintained at or slightly above the melting point of the Group 1 metal (i.e., approximately 700C to 1500C) and agitated for between several minutes to several hours. Generally speaking, higher reaction temperatures convert the material in shorter times. The reaction to form Stage I materials is mildly exothermic, and, on a large scale, the process would be preferably done by adding the liquid metal or alloy to the porous metal oxide with continual mixing, in such a way as to remove heat as it is produced. The reaction appears to form an alkali metal - porous metal oxide lattice. The exothermic nature of the reaction differentiates Stage I material from Stage 0 material. Heating above the exotherm can convert Stage I material to higher stage materials, depending upon the temperature.
[0054] When low-melting Group 1 metals are added to calcined and outgassed porous metal oxide in a closed environment such as an Erlenmeyer flask, the system often becomes warm because of exothermic reactions between the alkali metal and the porous metal oxide or its defect sites. This can result in the formation of mixtures of Stages 0 and I. The simplest and most direct preparation of Stage I materials is to heat Stage 0 samples overnight under an inert atmosphere at temperatures of 150 0C. Other times and temperatures may work also, but care should be taken to avoid overheating, which can lead to the formation of higher stage materials. To insure a homogeneous product, provision should be made for agitation during the heating process.
[0055] The Stage I material is an amorphous, black powder that does not immediately react with dry air, but reacts exothermically with water. A DSC of the Stage I material shows little or no Group 1 metal remaining within the porous metal oxide. The difference between Stages I and 0 is that the former can be handled in dry air and even quickly transferred in ordinary laboratory air without catching fire or degrading rapidly. When kept under an atmosphere of dry oxygen for hours to days, Stage I material (in contrast to Stage 0 material, which reacts which dry O2) is unchanged and produces the same amount of hydrogen gas upon reaction with liquid water as do fresh samples.
[0056] Stage I material has many uses in reactive chemistry as an active reducing agent, and for hydrogen production.
[0057] Thermal Behavior
[0058] Group 1 metals react exothermically with the porous metal oxide compositions of the invention. The Differential Scanning Calorimetry (DSC) trace shown in Figure 1 for a mixture of 2.9 mg of solid sodium metal and 8.0 of porous alumina (Al2O3) in the DSC pan has a sodium melting endotherm at 98 0C (ΔH = 89 J/g Na) followed at 280 - 380 °C by a multiple exotherm with ΔH = - 235 kJ per mole of Na. This is so large that it must represent a chemical reaction between Na and Al2O3. The dashed line is a repeat scan that shows no major thermal peaks. In figure 1, the solid line represents the first scan, and the dashed line represents a repeat scan.
[0059] Figure 2 shows a Differential Scanning Calorimetry (DSC) trace for a similar mixture of 8.2 mg of porous titanium dioxide (TiO2) and 3.0 mg of Na metal in the DSC pan. The DSC trace shows the Na melting endotherm at 98 0C (ΔH = 107 J/g Na) followed at 330 0C by an exotherm with ΔH = - 43.2 kJ per mole of Na (ΔH = -1.88 kJ/g Na). Thus, we presume that the exothermic peaks observed with various Group 1 metal/porous metal oxide compositions in the DSC traces shown in Figures 3-6 represent similar reduction reactions. [0060] For example, Figure 3 shows a Differential Scanning Calorimetry (DSC) trace for a 14.9 mg sample of Stage 0, 25 wt% Na2K-TiO2 prepared according to the procedure discussed in Example 2. Note the absence of a melting endotherm and the substantial exotherms as reaction between the metal and the TiO2 occurs. Figure 4 shows a Differential Scanning Calorimetry (DSC) trace for a 6.0 mg sample of Stage I, 25 wt% Na2K-TiO2 that had been heated to 150 0C overnight, as discussed in Example 2. Figure 5 shows a Differential Scanning Calorimetry (DSC) trace for an 11.7 mg sample of Stage 0, 25 wt% Na2K-Al2O3 prepared according to the procedure discussed in Example 1. The inset shows the melting endotherm of Na2K absorbed in the pores of the Al2O3. Broad exotherms are also evident from 50 - 250 0C. Figure 6 shows a Differential Scanning Calorimetry (DSC) trace for a 44.7 mg sample of Stage I, 21 wt% Na2K-Al2O3 prepared according to the procedure discussed in Example 3. Finally, Figure 7 shows a 1H NMR spectrum of the product of reduction (with Stage I, 25 wt% Na2K-Al2O3) of benzyl chloride in d-8 tetrahydrofuran (THF) prepared according to the procedure discussed in Example 5. The major product is bibenzyl. The aromatic region is on the left and the aliphatic region is on the right. The major peak of bibenzyl is at 2.86 ppm. The small peaks to the left are from THF and the small peak at 2.27 ppm is from the minor product, toluene.
[0061] Reaction Chemistry of the Group 1 Metal/Porous Metal Oxide Compositions
[0062] All Group 1 metal/porous metal oxide compositions of the invention react with water exothermically to produce hydrogen. Thus, advantageously, the compositions of the invention retain the reactivity of the Group 1 metal. Stage 0 material can be handled briefly in dry air, but it reacts slowly with oxygen and rapidly with moisture. By contrast, Stage I of the Group 1 metal/porous metal oxide compositions are unreactive towards dry oxygen. As shown in Example 7, the porous alumina yields recyclable alumina. Accordingly, the porous alumina yields an effective way to dry solvents by contacting the solvent with the porous alumina, thereby removing any water without consuming the porous alumina. This drying may be implemented either through a column or by a batch process. [0063] Although the Stage I Group 1 metal/porous metal oxide compositions of the invention are relatively innocuous and not violently reactive, they do have a strong base present and form alkali metal hydroxides upon reaction with water. In contrast to the reaction products of silica gel-based materials that are completely soluble, the alumina based materials of the invention form a solid white reaction product that can be recycled merely by washing with water and re-calcining at 600 0C as shown in Example 6. The titanium oxide based materials of the invention form a black solid upon reaction with water. [0064] Each stage of the Group 1 metal/porous metal oxide composition of the invention may be used as a reducing agent reacting with a number of reducible organic materials in the same manner known for alkali metals and their alloys. For example, the Group 1 metal/porous metal oxide compositions may be used to reduce aromatic compounds to their radical anions as is common in the so-called Birch reductions, commonly carried out with alkali metal - ammonia solutions. A Birch reduction is a general method of reduction of aromatic compounds by alkali metals in liquid ammonia. The theoretical and preparative aspects of the Birch reduction have been discussed in several reviews. {See, G. W. Watt, Chem. Rev., 46, 317 (1950); A. J. Birch, Quart .Rev. (London), 4, 69 (1950); A. J. Birch and H. F. Smith, Quart. Rev. (London), 12, 17 (1958); and C. D. Gutsche and H. H. Peter, Org. Syntheses, Coll. Vol. 4, 887 (1963).). The Group 1 metal/porous metal oxide compositions of the invention readily form aromatic radical anions with both naphthalene and anthracene in tetrahydrofuran (THF) solutions. Thus, they could be substituted for the sodium in Birch reductions. Example 4 shows a reduction reaction that uses a Group 1 metal/porous metal oxide composition of the invention.
[0065] Similarly, violent reductions such as the Wurtz reduction of halogenated organic compounds such as PCB 's might be carried out under controlled conditions. The
Wurtz reaction is the coupling of two organic radicals (R) by treating two moles of the organic halides (RX) with two moles of sodium:
2 RX + 2 Na → R-R + 2 NaX
{See A. Wurtz, Ann. CUm. Phys. [3] 44, 275 (1855); Ann. 96, 364 (1855).; J. L. Wardell, Comp. Organometal. Chem. 1, 52 (1982); W. E. Lindsell, ibid. 193; B. J. Wakefield, ibid. 7, 45; D. C. Billington, Comp. Org. Syn. 3, 413-423 (1991).). The Group 1 metal/porous metal oxide compositions of the invention can be readily substituted for the sodium in a Wurtz reaction or other such dehalogentation reaction. Compositions of the invention have also been used to dehalogenate inorganic halides. Example 5 shows a Wurtz reduction using a Group 1 metal/porous metal oxide composition of the invention.
[0066] Use of the Group 1 metal/porous metal oxide compositions of the invention allow alkali metal reactions such as those described above to be carried out under safer conditions due to the safer handling of the compositions over the corresponding alkali metal or alloy. Use of the compositions also generally gives higher yields than the corresponding reaction with just the Group 1 metal.
[0067] Because Stage I material (such as a Stage I Na2K/porous metal oxide composition) is very easy to prepare and retains much of the reducing ability of the parent Group 1 metal, it is likely to find use as a powerful and convenient reducing agent. Small glass columns filled with the Stage I powder are able to reduce a variety of organic compounds when they are dissolved in tetrahydrofuran (THF) and passed through the column. Alternatively, batch reactions can be carried out simply by stirring THF solutions of the organic compounds with the Stage I material. For example, as is shown below, benzophenone (1) is reduced to the radical anion (ketyl); and benzyl chloride (2) undergoes Wurtz reduction to form bibenzyl (3).
[0068] Numerous other reactions of Stage I materials are possible and likely. For example, they can reduce naphthalene to the radical anion and can convert benzyl chloride (2) to bibenzyl (3). The reduction of the representative compounds discussed above indicate that the Group 1 metal/porous metal oxide compositions of the invention can reduce aromatic
compounds to the radical anions or dianions and completely dechlorinate aromatic chlorides. This material might therefore be able to destroy PCB 's by dechlorination. The powerful reducing properties of the Group 1 metal/ porous metal oxide compositions of the invention also permit the use of chromatographic columns packed with this material for the reduction of organic and inorganic compounds that are now reduced by Na-K or alkali metal-ammonia solutions.
[0069] A major use for both stages of reduced porous metal oxide compositions of the invention is in the fuel storage potential and the formation of hydrogen gas needed for mobile fuel cells. For example, large stocks of the reduced porous metal oxide powder might be kept on conveyor trays within a holding tank. Addition to water would liberate pure hydrogen gas plus water vapor. Both stages of reduced porous alumina produce near quantitative amounts of the hydrogen that would have been produced from the alkali metal used. The hydrogen could then be used to power mobile fuel cells. For example, stocks of the Group 1 metal/porous metal oxide compositions might be kept on conveyer trays within a holding tank. Water is then introduced and the mixing with the water would liberate hydrogen which can then be extracted and compressed or pressurized. The compressed hydrogen would be used to fill mobile fuel cells. The spent powder, at this stage is now just porous metal oxide that could be reactivated with new Group 1 metal or used for other purposes. [0070] Examples
[0071] Example 1: Exemplary porous metal oxides. Porous TiO2 (Anatase) from
Sachtleben Chemie, (29.5 nm diameter pores, or 295 A) and activated porous alumina (358 m2/g) from Almatis AC were calcined in air at 600 °C and then cooled to room temperature. To these powders in a helium-filled glove box was added liquid Na2K dropwise onto the porous oxide in a stainless steel tray. The liquid alloy was quickly absorbed into the porous metal oxides. As long as the overall concentration of metal did not exceed 30 wt%, the white powder turned to dark black in color and the mixture became a uniform loose powder. This provided samples of Stage 0 material, as shown in Figure 5.
[0072] Example 2: One significant feature of the Group 1 metal/porous metal oxide compositions of the invention is their ability to produce pure hydrogen gas upon addition to water. The "reducing power" of the Group 1 metal/porous metal oxide compositions was determined by adding water to an evacuated sample and collecting hydrogen with a modified Toeppler pump. The reducing power is defined as the weight percent of alkali metal or alloy used that would produce the same amount of hydrogen. This was verified by collecting the hydrogen produced from a known mass of material upon reaction with out-gassed water. The
hydrogen was collected in a calibrated pipette using a modified Toeppler pump (mercury filled). Such analyses were run on every sample of reduced porous metal oxide, regardless of the stage of the material. For example, if a 30 wt% sample of NaK in Stage I porous metal oxide produced the same amount of hydrogen as would be produced by that amount of NaK alone, the reducing power would be 30%. The total amount of alkali metal hydroxide formed was then determined by the addition of HCl and back-titration with sodium hydroxide. The difference between the total alkali metal percentage as obtained from the titration and the reducing power is presumably a measure of the concentration of OH groups and other sources of hydrogen present on the porous metal oxide. Alkali metals can react with such groups during sample preparation to release hydrogen. This reaction is presumably the origin of the detectable amounts of gas formed during the mixing of the metal or alloy with the porous metal oxide. Except for the addition to porous TiO2, the amount of hydrogen produced was generally within 90 - 95% of the amount that would have been produced by the metal(s) alone. When Na2K-TiO2 or Na-TiO2 was used, the amount of hydrogen was reduced by an amount equivalent to about 10% metal. For example, a Stage 0 sample that was prepared with 25 wt% Na2K yielded hydrogen equivalent to only 13 wt% metal and another sample with 12 wt% metal yielded hydrogen equivalent to only 3 wt% Na2K, as shown in Figure 3. A sample of Stage I Na-TiO2 made with 25 wt% Na yielded hydrogen equivalent to only 16 wt% metal. By contrast, a sample of Stage I Na2K-Al2O3 with 30 wt% metal yielded hydrogen equivalent to 27 wt% metal. Even after exposure to dry air for two hours, the hydrogen yield corresponded to 23 wt % metal, indicating some reaction with air, but only moderate reactivity.
[0073] Example 3: The preparation of Stage I material can be performed by continuous heating of Stage 0 materials to 150 0C or by using the higher melting alkali metals, such as sodium and potassium. Outgassed and calcined porous alumina 14.0 g, was weighed out and, together with 6.0 g of Na metal, was introduced into a Parr Stainless steel reactor equipped with a Teflon gasket seal. The combination of porous metal oxide and Na was heated while rotating the reactor end-over-end at 60 rpm, first to 105 0C for 1 hr, then overnight at 155 0C. The powder was loose, black and free flowing. Similar processes to convert Stage 0 Na2K-Al2O3, Na2K-TiO2 and Na-TiO2 to Stage I materials were also carried out. For example, a DSC of 21 wt% material is shown in Figure 6.
[0074] Example 4. All of the alkali metal-porous metal oxide powders, whether
Stage 0 or Stage I, are able to reduce naphthalene and anthracene to the corresponding radical anions The reduction was observed by the formation of an intense green or blue color of the
solutions, respectively. These radical anions are stable enough to persist in solution for many hours. This reaction can be performed using several reaction setups, such as a batch reaction, or a chromatographic column loaded with the reducing material of the invention. The reaction with anthracene may be illustrated as is shown below.
[0075] Example 5: One of the earliest reactions of alkali metals with organic compounds is the Wurtz reaction in which de-halogenation of a chlorocarbon results in coupling to form a new carbon-carbon bond. When used with a bulk alkali metal and the neat chlorocarbon however, the reaction can be dangerously explosive. As is shown below, this coupling reaction was carried out with benzyl chloride dissolved in THF by reduction with both Stage I Na2K-TiO2 and Stage I Na2K-Al2O3 (-25 wt% Na2K). The former was done by passage though a small column made from a Pasteur pipet and filled with the reducing material and the latter was done in a batch reaction. The only product detected by 1H NMR was bibenzyl (See Figure 7)
[0076] Example 6. To check the ability to recycle Stage I Na2K-Al2O3, about 7.5 g of this material was reacted with water, resulting in the formation of copious amounts of a white residue. This was washed five times (with centrifugation each time) and dried. The dried powder was then calcined at 600 0C and brought into the helium-filled glove box. The recovered sample weighed 5.0 g and was combined drop-wise with 1.86 g of Na2K to form a loose black powder with a nominal metal concentration of 27.3 wt%. Hydrogen collection from this re-constituted Na2K-Al2O3 yielded hydrogen equivalent to 20.8 wt % metal. Although the recovery procedure does not give 100% of the starting material, these results show that Stage I Na2K-Al2O3 can be recycled by washing and calcinations. Thus, the same sample of Al2O3 could be re-used simply by washing, heat treatment, and re-introduction of alkali metals.
Claims
1. A Group 1 metal/porous metal oxide composition comprising the product of: mixing a liquid Group 1 metal with porous metal oxide selected from porous titanium oxide and porous alumina in an inert atmosphere under isothermal conditions sufficient to absorb the liquid Group 1 metal into the porous metal oxide pores, wherein the Group 1 metal/porous metal oxide composition produced reacts with dry O2.
2. The Group 1 metal/porous metal oxide composition of claim 1 wherein said porous metal oxide has 50 to 1,000 A diameter pores.
3. The Group 1 metal/porous metal oxide composition of claim 1 wherein the Group 1 metal is selected from the group consisting sodium, potassium, rubidium, cesium, and an alloy of two or more Group 1 metals.
4. The Group 1 metal/porous metal oxide composition of claim 1 wherein the mixing of the liquid Group 1 metal and the porous metal oxide selected from porous titanium oxide and porous alumina occurs at ambient temperature.
5. A Group 1 metal/porous metal oxide composition comprising the product of mixing a liquid Group 1 metal with porous metal oxide selected from porous titanium oxide and porous alumina under exothermic conditions sufficient to absorb the liquid Group 1 metal or liquid Group 1 metal alloy into the porous metal oxide pores, wherein the Group 1 metal/porous metal oxide composition produced does not react with dry O2.
6. The Group 1 metal/porous metal oxide composition of claim 5 wherein the pores of said porous metal oxide have an average pore size of approximately 50 to 1,000 A.
7. The Group 1 metal/porous metal oxide composition of claim 5 wherein the Group 1 metal is selected from the group consisting of sodium, potassium, rubidium, cesium, an alloy of two or more Group 1 metals.
8. The Group 1 metal/porous metal oxide composition of claim 5 wherein the Group 1 metal is present in an amount up to 30% by weight.
9. A Group 1 metal/porous metal oxide composition comprising the product of: mixing a liquid Group 1 metal with porous metal oxide selected from porous titanium oxide and porous alumina under exothermic conditions sufficient to absorb the liquid Group 1 metal into the porous metal oxide pores and heating the resulting mixture to a temperature of at least 1500C, wherein the Group 1 metal/porous metal oxide composition produced does not react with dry O2.
10. The Group 1 metal/porous metal oxide composition of claim 9 wherein the pores of said porous metal oxide have an average pore size of approximately 50 to 1,000 A.
11. The Group 1 metal/porous metal oxide composition of claim 9 wherein the Group 1 metal is selected from the group consisting of sodium, potassium, rubidium, cesium, and an alloy of two or more Group 1 metals.
12. The Group 1 metal/porous metal oxide composition of claim 9 wherein the Group 1 metal is present in an amount up to about 30% by weight.
13. A method of preparing a Stage 0 Group 1 metal/porous metal oxide composition comprising the step of contacting a liquid Group 1 metal with porous metal oxide selected from porous titanium oxide and porous alumina under isothermal conditions an inert atmosphere or under a vacuum to absorb the Group 1 metal into the pores of the porous metal oxide.
14. A method of preparing a Stage 0 Group 1 metal/porous metal oxide composition of claim 13 wherein the liquid Group 1 metal is contacted with the porous metal oxide selected from porous titanium oxide and porous alumina at ambient temperature.
15. A method of preparing a Stage I Group 1 metal/porous metal oxide composition comprising the step of: heating the Stage 0 Group 1 metal/porous metal oxide composition of claim 13 to 1500C for a time and under conditions to convert Stage 0 Group 1 metal/porous metal oxide composition to a Stage I Group 1 metal/porous metal oxide composition.
16. A method of preparing a Stage I Group 1 metal/porous metal oxide composition comprising the step of mixing a liquid Group 1 metal with porous metal oxide selected from porous titanium oxide and porous alumina under exothermic conditions sufficient to absorb the liquid Group 1 metal or liquid Group 1 metal alloy into the porous metal oxide pores.
17. A method for producing hydrogen gas comprising the step of contacting a Group 1 metal/ porous metal oxide composition of claim 1 with water.
18. A method for producing hydrogen gas comprising the step of contacting a Group 1 metal/porous metal oxide composition of claim 5 with water.
19. A method for producing hydrogen gas comprising the step of contacting a Group 1 metal/porous metal oxide composition of claim 9 with water.
20. A reduction reaction of an organic compound in the presence of an alkali metal, the improvement comprising conducting the reaction in the presence of a Group 1 metal/porous metal oxide composition of claim 1.
21. A reduction reaction of an organic compound in the presence of an alkali metal, the improvement comprising conducting the reaction in the presence of a Group 1 metal/porous metal oxide composition of claim 5.
22. A reduction reaction of an organic compound in the presence of an alkali metal, the improvement comprising conducting the reaction in the presence of a Group 1 metal/porous metal oxide composition of claim 9.
23. A reduction reaction of an organic compound in the presence of an alkali metal of claim 20, wherein the reduction reaction is a dehalogenation reaction or a Wurtz reaction.
24. A reduction reaction of an organic compound in the presence of an alkali metal of claim 21, wherein the reduction reaction is a dehalogenation reaction or a Wurtz reaction.
25. A reduction reaction of an organic compound in the presence of an alkali metal of claim 22, wherein the reduction reaction is a dehalogenation reaction or a Wurtz reaction.
26. A method of drying an organic solvent comprising the step of contacting an organic solvent with porous alumina for a sufficient time to remove water from the solvent.
27. A method of drying an organic solvent of claim 26, wherein the contacting step is done by batch or through a column.
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| EP05800331A EP1807199A4 (en) | 2004-09-22 | 2005-09-22 | Titanium oxide and alumina alkali metal compositions |
| AU2005289819A AU2005289819A1 (en) | 2004-09-22 | 2005-09-22 | Titanium oxide and alumina alkali metal compostions |
| CA2580930A CA2580930C (en) | 2004-09-22 | 2005-09-22 | Titanium oxide and alumina alkali metal compositions |
| JP2007533609A JP5048503B2 (en) | 2004-09-22 | 2005-09-22 | Titanium oxide and alumina alkali metal composition |
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| DE102009008144A1 (en) | 2009-02-09 | 2010-08-19 | Nano-X Gmbh | Process for the preparation of alkali and alkaline earth alloys and use of the alkali and alkaline earth alloys |
| JP2010540558A (en) * | 2007-09-28 | 2010-12-24 | シグナ・ケミストリー・インコーポレイテッド | Use of alkali metal-silica gel (M-SG) materials in the drying and purification of solvents and monomers for their use in anionic polymerization |
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| CN101573179A (en) * | 2006-09-08 | 2009-11-04 | 西格纳化学有限责任公司 | Lithium-porous metal oxide compositions and lithium reagent-porous metal compositions |
| EP2970337A4 (en) * | 2013-03-15 | 2016-11-16 | Signa Chemistry Inc | Treatment of alkali silica gel and alkali porous metal oxide compositions |
| EP3120405B1 (en) | 2014-03-19 | 2019-11-20 | Intelligent Energy Ltd | Flexible fuel cell power system |
| EP3590947B1 (en) | 2017-02-28 | 2021-08-18 | Kyushu University, National University Corporation | Method for producing transition metal-isocyanide complex |
| US20200001285A1 (en) | 2017-02-28 | 2020-01-02 | Kyushu University, National University Corporation | Catalyst for hydrosilylation reaction, hydrogenation reaction, and hydrosilane reduction reaction |
| JP2020138922A (en) * | 2019-02-27 | 2020-09-03 | 株式会社神鋼環境ソリューション | Method of preparing dehydration solvent |
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- 2005-09-22 EP EP05800331A patent/EP1807199A4/en not_active Ceased
- 2005-09-22 US US11/232,077 patent/US7259128B2/en active Active
- 2005-09-22 CA CA2580930A patent/CA2580930C/en not_active Expired - Fee Related
- 2005-09-22 JP JP2007533609A patent/JP5048503B2/en not_active Expired - Fee Related
- 2005-09-22 CA CA2799535A patent/CA2799535C/en not_active Expired - Fee Related
- 2005-09-22 WO PCT/US2005/033823 patent/WO2006036697A2/en active Application Filing
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2007
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010540558A (en) * | 2007-09-28 | 2010-12-24 | シグナ・ケミストリー・インコーポレイテッド | Use of alkali metal-silica gel (M-SG) materials in the drying and purification of solvents and monomers for their use in anionic polymerization |
| DE102009008144A1 (en) | 2009-02-09 | 2010-08-19 | Nano-X Gmbh | Process for the preparation of alkali and alkaline earth alloys and use of the alkali and alkaline earth alloys |
| US9249480B2 (en) | 2009-02-09 | 2016-02-02 | Nano-X Gmbh | Method for producing alkali and alkaline earth alloys and use of the alkali and alkaline earth alloys |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2006036697A3 (en) | 2006-05-04 |
| US20090266771A1 (en) | 2009-10-29 |
| EP1807199A4 (en) | 2010-11-10 |
| US20060073968A1 (en) | 2006-04-06 |
| JP2008513347A (en) | 2008-05-01 |
| CA2580930C (en) | 2013-07-09 |
| AU2005289819A1 (en) | 2006-04-06 |
| US7820061B2 (en) | 2010-10-26 |
| EP1807199A2 (en) | 2007-07-18 |
| US7560606B2 (en) | 2009-07-14 |
| CA2799535C (en) | 2016-08-02 |
| US7259128B2 (en) | 2007-08-21 |
| JP5048503B2 (en) | 2012-10-17 |
| US20080063596A1 (en) | 2008-03-13 |
| CA2580930A1 (en) | 2006-04-06 |
| CA2799535A1 (en) | 2006-04-06 |
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