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1. 发明专利

DE1814541C3 未知
公开(公告)号：DE1814541C3
公开(公告)日：1981-02-26
申请号：DE1814541
申请日：1968-12-13
申请人： EXXON RESEARCH AND ENGINEERING CO., LINDEN, N.J. (V.ST.A.)
发明人： JONES, TERREL M., MORRIS PLAINS, N.J. (V.ST.A.)
IPC分类号： B63B3/20 , B63B5/14 , B63B5/20 , B63B25/16

2. 发明专利

DE2411672B2 未知
公开(公告)号：DE2411672B2
公开(公告)日：1981-02-05
申请号：DE2411672
申请日：1974-03-12
申请人： EXXON RESEARCH AND ENGINEERING CO., LINDEN, N.J. (V.ST.A.)
发明人： LYON, RICHARD K., FANWOOD, N.J. (V.ST.A.)
IPC分类号： B01D53/56 , C01B21/02 , F23C99/00 , F23J15/00 , B01D53/34
摘要： 1465856 NO reduction EXXON RESEARCH & ENG CO 27 Feb 1974 [16 March 1973] 8861/74 Heading C1A NO in combustion gas is chemically reduced by contacting with 0À4-10 moles of NH 3 per mole NO in the presence of oxygen and of a substance which is gaseous and readily oxidized below 1600 F., the contacting being performed at 1300-2000 F. NH 3 may be provided by a precursor, such as a solution of NH 3 , ammonium formate, oxalate or carbonate, and the reducing material may be H 2 , a paraffin, olefine or aromatic hydrocarbon, sulphonated hydrocarbons, CO, and organic hydrocarbons containing O or N.

3. 发明专利

DE1919492C3 未知
公开(公告)号：DE1919492C3
公开(公告)日：1980-10-02
申请号：DE1919492
申请日：1969-04-17
申请人： EXXON RESEARCH AND ENGINEERING CO., LINDEN, N.J. (V.ST.A.)
发明人： CLARKE, JAMES S., CRANFORD, N.J. (V.ST.A.) , KARCHER, GUIDO G., OXSHOTT, SURREY (VER. KOENIGREICH)
IPC分类号： F17C3/02 , F17C13/00 , F17C3/04

5. 发明专利

DE2120126B2 未知
公开(公告)号：DE2120126B2
公开(公告)日：1980-09-18
申请号：DE2120126
申请日：1971-04-24
申请人： EXXON RESEARCH AND ENGINEERING CO., LINDEN, N.J. (V.ST.A.)
发明人： GUERRE, ROBERT P., DOVER , RULAND, ROSS R., HOPATCONG
IPC分类号： F23C7/00 , F23D11/36
摘要： 1341253 Vortex burners ESSO RESEARCH & ENG CO 19 April 1971 [6 July 1970] 26452/71 Heading F4T A vortex-type burner for the combustion of oil or gas fuel from a gun 37 with air from an inlet and plenum chamber in the burner casing 12 comprises a swirl chamber in a casing 22 for receiving a predetermined fraction of the air inlet flow and setting up a vortex with the injected fuel, and annular refractory tiles 42 and 45 shaped so as to define a uniform annular air gap 39 between them and a second such gap 40 between the tile 45 and a support plate 49, the remainder of the inlet air being directed through these gaps 39 and 40 to shape and contain the flame without the use of a combustion chamber and to aid combustion by creating turbulences to recirculate hot gases to the combustion zone. The inlet air may be preheated or ambient and its speed of flow through gaps 39 and 40 can be changed by adjusting the gap widths by means of bolts, which air flowing in the gaps must comprise at least half of the inlet air. In a modification of this construction the upper surface 51 of tile 45 and the support plate 49 slope inwardly so that gap 40 is inclined to the horizontal. In an alternative embodiment only one air gap is provided which is formed between parallel surfaces of two annular tiles. The burner casing is lined with block insulation and a pilot system may be incorporated. The burner is described as being mounted on a furnace floor 11 or wall.

6. 发明专利

DE2161321B2 未知
公开(公告)号：DE2161321B2
公开(公告)日：1980-08-07
申请号：DE2161321
申请日：1971-12-10
申请人： EXXON RESEARCH AND ENGINEERING CO., LINDEN, N.J. (V.ST.A.)
发明人： CRAWFORD, HARRY MILES, PORT MURRAY, N.J. (V.ST.A.)
IPC分类号： G01N27/00 , G01N33/18 , G01N29/02

7. 发明专利

DE2066059B1 未知
公开(公告)号：DE2066059B1
公开(公告)日：1980-05-14
申请号：DE2066059
申请日：1970-01-29
申请人： EXXON RESEARCH AND ENGINEERING CO., LINDEN, N.J. (V.ST.A.)
发明人： PATTON, TAD L., BAYTOWN, TEX. (V.ST.A.)
IPC分类号： C08G18/00 , C08G18/02 , C08G18/30 , C08G18/38 , C08G73/00 , C08G73/06 , C07C121/417 , C07C120/00
摘要： 1298521 1,3 - Imidazolidine - 1,3 - diyl - ring- containing polymers ESSO RESEARCH & ENG CO 19 Jan 1970 [3 Feb 1969 (2)] 2437/70 Heading C3R A polymer has a structure of alternating organic moieties (R) and 1,3-imidazolidine-1,3- diyl rings predominantly or both rings randomly or alternately distributed. The polymer is soluble in dipolar aprotic solvents. The moieties (R) may be aliphatic, alicyclic, and/or aromatic, or derivatives thereof containing functional groups which do not reach with an isocyanate group; such groups may be, e.g. alkyl, aryl, halogen, sulphoxy, sulphonyl, alkoxy, aryloxy, oxo, ester, alkylthio or nitro; but not carboxylic acid, phenol or amine. Moieties (R) may be all the same, or there may be 2 or more different (R), which may be randomly or alternately distributed. (R) may be one or more of the following, or a divalent group formed therefrom: diphenylmethane; diphenyl ether; tetramethylene, hexamethylene, dodecamethylene, or 2,2,4-trimethylhexamethylene, or dipropylether; m- or p-phenylene, biphenylene, 1,5-naphthalene, isophorone, 1,4-cyclohexane, toluene, durene, 4,41-diphenylmethane, 3,3 1 -dimethyl-4,4 1 -biphenylene, 4,4 1 - diphenyl-isopropylidene, m- or p-xylylene, 4,4 1 - methylenebis - (cyclohexyl), cyclohexylphenyl, or benzyl; diphenyl sulphone, diphenyl ether, dimethoxybiphenylene; tetrafluorophenylene; octafluorobiphenyl. The polymer is made by a reaction, initiated by an added CN- catalyst between: (a) HCN and diisocyanate(s); (b) dicyanoformamide(s) and diisocyanate(s); or (c) by polymerization of cyanofonnamidyl isocyanate(s). The catalyst may be NaCN. The dicyanoformamide(s) for (b), and the cyanoformamidyl isocyanate(s) for (c), may each be prepared by reacting diisocyanate(s) and HCN. The solvent is preferably a dipolar aprotic solvent, e.g. dimethyl formamide, dimethylacetamide, dimethyl sulphoxide, or N-methylpyrrolidone. It must be anhydrous. In all processes, the reaction may be initiated at 0-60 C. The temperature may be regulated to 140 C. After the polymerization reaction has subsided, a tertiary amine may be added which catalyses the ring-closure of cyanoformylurea groups to imidazolidine ring. Examples are triethylamine, trimethylamine, N- methyl morpholine, N-methyl piperidine, or triethylene triamine; or N,N-dialkylanilines, pyridine, picoline or lutidine. There may be 0À0005-0À05 molar equiv. of amine based on isocyanate groups. The solution temperature is preferably 20-90 C. Precipitation of the polymer. Before the polymer is pptd., an active solvent may be added, e.g. alcohol or primary or secondary amine, to eliminate the isocyanate groups, to prevent cross-linking with the heterocyclic imino groups. The polymer is then pptd. by pouring into either a non-reactive solvent, e.g. benzene, toluene or acetone, or into a reactive solvent which reacts with the terminal isocyanate groups, e.g. an alkanol, primary or secondary amine, H 2 O, or NH 4 OH. Use.-Films, fibres, foams, moulded objects, laminates or electrical insulators. Films may be made by forming under heat and pressure, or by casting from solution, e.g. in dimethyl formamide.

8. 发明专利

DE2530810C3 未知
公开(公告)号：DE2530810C3
公开(公告)日：1980-01-10
申请号：DE2530810
申请日：1975-07-10
申请人： EXXON RESEARCH AND ENGINEERING CO., LINDEN, N.J. (V.ST.A.)
发明人： LUNDBERG, ROBERT D., SOMERVILLE , MAKOWSKI, HENRY S., SCOTCH PLAINS , WESTERMAN, LOWELL, BAYTOWN, TEX.
IPC分类号： C08K5/00 , C08K5/04 , C08K5/05 , C08L7/00 , C08L21/00 , C08L23/00 , C08L25/00 , C08L101/00
摘要： Ionically crosslinked polymers are plasticized by blending the ionic compositions with a plasticizer which is normally liquid and non-volatile, the plasticizer compounds having a solubility parameter of at least 9.0. The plasticizers are preferential plasticizers for their ionic domains and do not ordinarily plasticize the polymeric backbone.

9. 发明专利

DE2027812B2 未知
公开(公告)号：DE2027812B2
公开(公告)日：1980-01-03
申请号：DE2027812
申请日：1970-06-05
申请人： EXXON RESEARCH AND ENGINEERING CO., LINDEN, N.J. (V.ST.A.)
发明人： MARSH, JOHN FREDERICK, OLD MARSTON, OXFORD (VER. KOENIGREICH)
IPC分类号： C07C309/28 , C07F5/02 , C10L1/30 , C10M169/00 , C11D1/00 , C07F5/04

10. 发明专利

DE1542105C3 未知
公开(公告)号：DE1542105C3
公开(公告)日：1979-11-15
申请号：DEE0029645
申请日：1965-07-06
申请人： EXXON RESEARCH AND ENGINEERING CO., LINDEN, N.J. (V.ST.A.)
发明人： BATZOLD, JOHN S., WESTFIELD, N.J. (V.ST.A.)
IPC分类号： B01J23/00 , B01J23/90 , B01J37/00 , H01M4/86 , H01M4/90 , H01M4/92 , H01M4/88
摘要： A finely divided catalyst is prepared by contacting a support with a salt solution of the catalytic metal, reducing the metal ions and subsequently removing the support. The resultant catalyst may be in the form of metal, e.g. Pt, Ru, Rh, Pd, Ir, Os, Re, Cr, V, Ti, Al, Mg, W, Mo, Au, Ag, Pb and Ce and alloys thereof, or metal oxide. The support material may be silica gel or alumina (removable by treatment with a strong alkali), calcium carbonate (removable by treatment with acid), ammonium oxalate or ammonium carbonate (removable by heating to 700 DEG F. or, in the case of ammonium carbonate, by immersion in hot water). The catalyst may be improved by co-reducing the desired catalytic material with a less noble compound; after removal of the support, the less noble component is removed by anodization or dissolution in acid.

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