Abstract:
High Capacity solid state cyanocobaltate complexes represented by the chemical formula:[(A).sub.a (R.sub.4 N).sub.b ].sup.z+.sub.x/z [Co(CN).sub.n ].sup.x- .multidot.pSwhere:A is alkali metal atom, alkaline earth metal atom, Zn, Cd or Hg atom;a is any number from 0 to 2.5each R is independently C.sub.1 -C.sub.1O substituted or unsubstituted alkyl, aryl or aralkyl; or a long chain hydrocarbon polymerb is any number from greater than zero to 3z is 1, 2 or 3;n is any number from 3 to 5;x is n-2;p is any number from greater than zero to 6; andS is a ligand which is capable of coordinating with [(A).sub.a (R.sub.4 N).sub.b 9 .sup.z+, Co or both.are capable of chemically binding oxygen to form novel oxygen adducts, thereby selectively removing oxygen from an oxygen-containing fluid stream. The bound oxygen may be recovered from the complexes by increasing the temperature or by reducing the partial pressure of O.sub.2 above the adduct.
Abstract translation:由[化学式为[(A)a(R4N)b] z + x / z [Co(CN)n] x-xpS表示的高容量固态氰钴酸盐络合物,其中:A为碱金属原子,碱土金属原子, Zn,Cd或Hg原子; a为0至2.5的任何数,每个R独立地为C 1 -C 10取代或未取代的烷基,芳基或芳烷基; 或长链烃聚合物b是大于0至3的任何数为1,2或3; n是从3到5的任何数字; x是n-2; p是从大于零到6的任何数字; 并且S是能够与[(A)a(R 4 N)b 9 z +,Co或两者配位的配体。 能够化学结合氧以形成新的氧加合物,从而从含氧流体物流中选择性地除去氧。 可以通过增加温度或通过降低加合物上方的O 2分压来从络合物中回收结合的氧。
Abstract:
Hydrogen is stored at cryogenic temperatures by adsorption on porous carbon having a nitrogen BET apparent surface area above about 1500 m.sup.2 /g. Hydrogen can be adsorbed and desorbed in the context of a cryopump, having as the pumping element a panel, having large particles of pressed porous carbon thereon.
Abstract:
A novel process is described for the homogeneous hydrogenation of nitriles to primary amines utilizing anionic Group VIII metal hydride compositions as catalysts which contain phosphorus, arsenic or antimony organoligands. Use of these anionic catalysts allows the high yield hydrogenation of nitriles to primary amines to be conducted under mild conditions of temperature and pressure with high selectivity and eliminates the need for the presence of ammonia to suppress the formation of significant amounts of secondary and tertiary amines.
Abstract:
A novel process is described for the homogeneous hydrogenation of carboxylic acid esters to primary alcohols utilizing anionic Group VIII metal hydride compositions as catalysts which contain phosphorus, arsenic or antimony organoligands. Use of these anionic catalysts allows the process to be conducted in solution under mild conditions of temperature and pressure with high selectivity and eliminates the disadvantages of utilizing heterogeneous catalysts. A process is also described for decarbonylating formate esters utilizing said compositions as catalysts.
Abstract:
An improved process is described for the homogeneous hydrogenation of polycyclic aromatic hydrocarbons utilizing anionic Group VIII metal hydride compositions as catalysts which contain phosphorus, arsenic or antimony organoligands. Use of these anionic catalysts allows the process to be conducted under mild conditions of temperature and pressure with high selectivity for the production of partially hydrogenated derivatives of polycyclic aromatic hydrocarbons such as 1,2,3,4-tetrahydronaphthalene, and eliminates the need for the presence of base or carbon monoxide atmosphere in the process.
Abstract:
Complexes of the titanium cyclopentadienyl compound ##STR1## and nitrogen, having the probable structure: ##STR2## where the symbol N.apprxeq.N represents a bonding state intermediate between the azo-N=N- bond and the hydrazine =N-N= bond; such complex having the simple dimeric form as indicated by molecular weight determination on this form dissolved in tetrahydrofuran, and having a polymeric form wherein a nitrogen atom of one molecule of the dimeric form is coordinated by a dative link with a Ti atom of another molecule of the dimeric form, as suggested by low solubility of this polymeric form in 1,2-dimethoxyethane and breakdown of this form to the dimeric form by action of tetrahydrofuran.Another related complex is a black solid nitrogen-containing reaction product of the above titanium cyclopentadienyl compound in dry state with nitrogen at about 60 atmospheres pressure, having an infrared spectrum typical of a metallocene compound with no N-N or Ti-N vibration absorption bands.The nitrogen in these complexes is reactive, e.g. with reducing agents such as potassium naphthalene, to afford ammonia. Moreover, the complexes are catalytically active for hydrocarbon conversions such as conversion of ethylene to ethane, butane, 1-butene and 1,3-butadiene.
Abstract:
A process is provided for selectively separating oxygen from an oxygen-containing fluid stream by bringing said fluid stream into contact with a high capacity solid state cyanocobaltate complex in a non-aluminosilicate environment represented by the chemical formula:A.sub.x/z.sup.z+ [Co(CN).sub.n ].sup.x- .multidot.pSwhere:A is an alkali, alkaline earth, transition, or Group 12 metal atom;z is 1, 2 or 3;n is any number from 3 to 5;x is n-2;p is any number from greater than zero to 6; andS is a ligand which is capable of coordinating with A.sup.z+, Co or both.These complexes chemically bind oxygen to form novel oxygen adducts, thereby selectively removing oxygen from the fluid stream. The bound oxygen may be recovered by increasing the temperature or by reducing the partial pressure of O.sub.2 above the adduct.
Abstract:
A process is disclosed for making a highly fluorinated aromatic compound by contacting a perfluorocycloalkane, such as perfluorodecahydronaphthalene, with a complex of a metal from Groups IA and IIA of the Periodic Table and an organic electron acceptor. The reaction is carried out in an organic solvent and under reducing conditions which are relatively moderate. Best results are obtained using a perfluorocycloalkane having 2-4 condensed rings and a complex of either sodium or lithium and benzophenone thereby making a perfluorinated condensed ring aromatic compound such as perfluoronaphthalene or perfluorophenanthrene.
Abstract:
The present invention is a process for reversibly absorbing acid gases, such as CO.sub.2, H.sub.2 S, SO.sub.2, HCN and the like from gas mixtures. The gas mixture containing one or more of these acid gases is contacted with a hydrated salt of the compositionA.sub.x.sup.m+ B.sub.y.sup.n-.rH.sub.2 Owherein A.sup.m+ is a cation, B.sup.n- is the conjugate base of a weak acid having a pKa corresponding to an ionization constant of the acid greater than 3 as measured in dilute aqueous solution, m and n are independently integers from 1-4, x and y are integers such that the ratio of x to y provides a neutral salt and r is any number greater than zero up to the maximum number of moles of water which can be bound to the salt. The salt hydrate reversibly absorbs the acid gas from the gas mixture.
Abstract:
The present invention is a process for separating ammonia from mixtures of other gases or from aqueous streams. The ammonia-containing mixture is contacted with a membrane containing, as the active component, a salt having the structural formula: NR.sub.4.sup.+ X.sup.-, wherein each R is independently H or a straight chain or branched alkyl group and X.sup.- is an organic or inorganic anion. The membrane is useful for the selective permeation of ammonia from mixtures of gases containing ammonia, nitrogen and hydrogen.