Purification process for aromatic acids
    31.
    发明授权
    Purification process for aromatic acids 失效
    芳香酸的净化过程

    公开(公告)号:US3847977A

    公开(公告)日:1974-11-12

    申请号:US26380972

    申请日:1972-06-19

    Inventor: NORTON R

    CPC classification number: C07C51/48

    Abstract: 1. A PROCESS FOR PURIFICATION OF AN AROMATIC ACID CONTAINING COLOR AND NITROGEN IMPURITIES SELECTED FROM HE GROUP OF POLY ACIDS OF THE BENZENES SERIES AND MONO- AND POLY ACIDS OF THE NAPHTHALENES SERIES AND OBTAINED BY THE HYDROLYSIS OF NITRILES, WHICH COMPRISES EXTRACTING SAID IMPURE ACID WITH A THREE PHASE HETEROGENEOUS SYSTEM CONSISTING ESSENTIALLY OF AN AQUEOUS SOLUTION OF ACETIC ACID, A LIQUID AROMATIC HYDROCARBON HAVING FROM SIX TO NINE CARBON ATOMS, AND AROMATIC ACID; THE AQUEOUS ACETIC ACID SOLUTION CONTAINING FROM ABOUT 40% TO ABOUT 65% BY WEIGHT OF WATER, THE WEIGHT RATIO OF AQUEOUS EXTRACTANT SOLUTION TO AROMATIC HYDROCARBON BEING FROM ABOUT 3:75:1 TO ABOUT 20:1, FROM ABOUT 15% TO ABOUT 90% BY WEIGHT OF THE AROMATIC ACID BEING IN THE SOLID PHASE, AND SAID EXTRACTION BEING MADE TO OCCUR IN A CLOSED SYSTEM AT A TEMPERATURE OF BETWEEN ABOUT 200* AND ABOUT 250* C.

    Method of preparing thermoset polymer coated-wax impregnated cellulosic stock
    32.
    发明授权
    Method of preparing thermoset polymer coated-wax impregnated cellulosic stock 失效
    制备热固性聚合物涂覆波纹胶体的方法

    公开(公告)号:US3844829A

    公开(公告)日:1974-10-29

    申请号:US32526573

    申请日:1973-01-22

    Inventor: BLACK E

    Abstract: Porous cellulosic stock can be coated with a thermoset polymer while being impregnated with a wax by this invention. A dispersion of solid particles of the precursor of a thermoset polymer in molten wax is applied to cellulosic stock at a temperature below the conversion temperature of the precursor. This treated cellulosic stock is then heated to a temperature above the conversion temperature of the precursor and subjected to pressure. The resulting laminated product is polymer coatedwax impregnated cellulosic stock. The solid precursor used must be substantially insoluble in the molten wax at a temperature below the conversion temperature of the precursor and must be convertible below a temperature which would degrade the stock. This product has utility as a packaging material comprising a high water vapor barrier coupled with a tough, scuff-resistant, non-blocking surface.

    Abstract translation: 多孔纤维素原料可以用热固性聚合物涂覆,同时通过本发明用蜡浸渍。 将熔融蜡中的热固性聚合物的前体的固体颗粒的分散体在低于前体的转化温度的温度下施加到纤维素原料上。 然后将经处理的纤维素原料加热到高于前体转化温度的温度,并承受压力。 所得层压产品是聚合物涂覆的蜡浸渍的纤维素原料。 所使用的固体前体必须在低于前体转化温度的温度下基本上不溶于熔融蜡中,并且必须在低于使得原料降解的温度下转化。 该产品具有作为包装材料的实用性,该包装材料包括与坚韧,抗磨损,无阻塞的表面相结合的高水蒸汽屏障。

    Ammoxidation process
    33.
    发明授权
    Ammoxidation process 失效
    氧化工艺

    公开(公告)号:US3839398A

    公开(公告)日:1974-10-01

    申请号:US31030672

    申请日:1972-11-29

    Inventor: LETO J POTTS J SHANG J

    CPC classification number: C07C253/28 C07C255/51 C07C255/52

    Abstract: 1. IN THE PROCESS OF CARRYING OUT AMMOXIDATIONREACTIONS IN A MOVING BED REACTOR USING V2O4 AS CATALYST AND WITHOUT ADDED OXYGEN, THE IMPROVEMENT WHICH COMPRISES: (A) SEPARATING SPENT CATALYST CONSISTING ESSENTIALLY OF V2O3 FROM AMMOXIDATION PRODUCTS AND UNCREATED STARTING MATERIALS, (B) OXIDIZING A PORTION OFF SAID V2O3 TO V2O5, (C) MIXING SAID V2O5 WITH REMAINING V2O3, (D) HEATING SAID MIXTURE TO A TEMPERATURE BETWEEN ABOUT 350* AND 500* C. WHEREBY V2O4 IS FORMED, AND (E) FEEDING SAID V2O4 TO SAID AMMOXIDATION PROCESS FOR USE AS CATALYST.

    Gasoline containing a methyl phenol and an ether
    34.
    发明授权
    Gasoline containing a methyl phenol and an ether 失效
    含有甲基酚和醚的汽油

    公开(公告)号:US3836342A

    公开(公告)日:1974-09-17

    申请号:US26585072

    申请日:1972-06-23

    CPC classification number: C10L1/18 C10L1/023 C10L1/1832 C10L1/1852

    Abstract: A useful fuel for an internal combustion engine comprises a hydrocarbon base stock of gasoline boiling range, a methylsubstituted phenol and an ether containing a branched alkyl group and boiling below 460*F., said phenol and said ether each being present in amount (e.g., 0.1-15 wt. %) sufficient to increase the Research octane number (RON). The invention also includes a gasoline blending system. For example, preferred compositions can be made by blending 89 RON gasoline containing 5 vol. % p-cresol with 97 RON gasoline containing 5% methyl methoxy propane. Beneficial synergism is noted in such blends for RON blending values.

    Abstract translation: 用于内燃机的有用燃料包括汽油沸程的烃基料,甲基取代的苯酚和含有支链烷基并沸点低于460°F的醚,所述苯酚和所述醚各自以 例如0.1-15重量%)足以增加研究辛烷值(RON)。 本发明还包括汽油混合系统。 例如,优选的组合物可以通过混合含有5体积% %对甲酚与含有5%甲基甲氧基丙烷的97RON汽油。 在这种RON混合值的混合物中注意到有益的协同作用。

    Dehydrocyclization of hydrocarbons
    35.
    发明授权
    Dehydrocyclization of hydrocarbons 失效
    烃的脱氢化

    公开(公告)号:US3832414A

    公开(公告)日:1974-08-27

    申请号:US31420772

    申请日:1972-12-11

    Inventor: OISHI M

    CPC classification number: B01J29/12 C07C5/417

    Abstract: Process of dehydrocyclizing C6-C10 hydrocarbons having at least a C6 backbone using a Li, Na or K zeolite X or Y impregnated or ion exchanged with 0.1 to 1.2 weight percent Pt and impregnated or ion exchanged with 0.01 to 1.0 weight percent Cd at from 500 to 560 and preferably 510* to 555*C. using a partial pressure of hydrogen of from 10 to 300 p.s.i. and preferably 40 to 200 p.s.i. to form benzene and alkylbenzene.

    Abstract translation: 使用Li,Na或K沸石X或Y进行脱氢环化C6-C10烃的工艺,该溶剂用0.1至1.2%(重量)的Pt进行浸渍或离子交换,并以0.01至1.0%(重量) 至560℃,优选510℃至555℃,使用10至300psi的氢分压 优选为40〜200p.s.i。 形成苯和烷基苯。

    Chlorination of hydrocarbons
    36.
    发明授权
    Chlorination of hydrocarbons 失效
    碳氢化合物的氯化

    公开(公告)号:US3819732A

    公开(公告)日:1974-06-25

    申请号:US85998269

    申请日:1969-09-22

    CPC classification number: C07C17/152

    Abstract: COMPOUNDS CONTAINING HYDROGEN BONDED TO CARBON ARE CHLORINATED IN VAPOR PHASE WHEN INTRODUCED AT AN INTERMEDIATE LEVEL INTO A REACTOR MAINTAINED AT A TEMPEATURE IN THE RANGE OF 315-500*C. AND CONTAINING A BED OF FERROUS CHLORIDE WHICH BY INTERACTION WITH HCL AND OXYGEN IS USED TO PRODUCE FERRIC CHLORIDE VAPOR WHICH IS CONTACTED WITH THE C-H CONTAINING COMPOUND TO PRODUCE HCL, A C-CL GROUP, AND SOLID FECL2 WHICH FALLS TO THE BED. WHEN THE BED OF FERROUS CHLORIDE GRADUALLY CONVERTS TO OXYGENATED IRON COMPOUND, THE BED CAN BE PERIODICALLY REGENERATED BY INCREASING THE PROPORTION OF HCL:O2 AND CONTINUING TO OPERATE AT THE HIGH HCL:O2 MOLAR PROPORTION UNTIL SUBSTANTIALLY ALL OF THE OXYGENATED IRON COMPOUND HAS BEEN CONVERTED TO IRON CHLORIDE.

    Preparation of 2-pyrrolidinone
    37.
    发明授权
    Preparation of 2-pyrrolidinone 失效
    2-吡咯烷酮的制备

    公开(公告)号:US3812149A

    公开(公告)日:1974-05-21

    申请号:US27412072

    申请日:1972-07-21

    Inventor: HOLLSTEIN E

    CPC classification number: C07D207/26

    Abstract: A PROCESS FOR PREPARING 2-PYRROLIDIONE WHICH COMPRISES REACTING SUCCINIC ACID OR ITS PRECURSOR, HYDROGEN, AND AMMONIA IN AN AQUEOUS SYSTEM AT A MOLE RATIO OF AMMONIA TO ACID OF ABOUT 1.1:1 TO ABOUT 1.7:1, AT A TEMPERATURE OF FROM ABOUT 250* C. TO ABOUT 275* C., AT A PRESSURE OF FROM ABOUT 1500 TO 2000 P.S.I.G., FOR A TIME OF ABOUT 3 TO ABOUT 6 HOURS, AND IN THE PRESENCE OF A RHODIUM CATALYST.

    Conversion of isobutane to isobutene
    38.
    发明授权
    Conversion of isobutane to isobutene 失效
    ISOBUTANE转换为ISOBUTENE

    公开(公告)号:US3787516A

    公开(公告)日:1974-01-22

    申请号:US3787516D

    申请日:1972-09-28

    Inventor: BEAN R

    CPC classification number: C07C5/46 C07C11/09

    Abstract: ISOBUTANE IS DEHYDROGENATED TO PRODUCE ISOBUTENE BY ESTABLISHING IN A FIRST O ZONE A DEHYDROGENATING AGENT CONSISTING ESSENTIALLY OF SULFUR AT 700-1000*C. AND THEN DIRECTLY CONTACTING SAME NON-CATALYTICALLY IN A SECOND ZONE AT 500-630*C. WITH ISOBUTANE. ESTABLISHMENT OF THE DEHYDROGENATING AGENT CAN BE DONE EITHER BY CATALYTICALLY REACTING SO2 AND H2S AT 700-1000*C. OR BY HEATING SULFUR TO 700-1000*C.

    Preparation of 2,7-dimethylnaphthalene
    40.
    发明授权
    Preparation of 2,7-dimethylnaphthalene 失效
    制备2,7-二甲基苯乙烯

    公开(公告)号:US3775500A

    公开(公告)日:1973-11-27

    申请号:US3775500D

    申请日:1972-08-09

    Inventor: THOMPSON S

    CPC classification number: C07C15/24 Y10S585/926

    Abstract: A MULTISTEP PROCESS IS DISCLOSED WHEREIN 5-P-TOLYLPENTENE-2 IS CONVERTED TO 1,7-DIMETHYLTETRALIN IN THE PRESENCE OF A SOLID ACIDIC CARALYST AT 200-450*C. AND PREFERABLY ALSO RECYCLED HYDROGEN, VAPORS FROM THIS CONVERSION ARE REACTED BY CONTACT AT 300-500*C. IN A HYDROGEN ATMOSPHERE WITH A SOLID DEHYDROGENATION CATALYST, PREFERABLY PLATINUM ON NON-ACIDIC ALUMINA, TO FORM 1,7-DIMETHYLNAPHTHALENE AND HYDROGEN, VAPORS FROM THE DEHYDROGENATION REACTION ARE CONTACTED WITH 275-500*C. WITH A SOLID ACIDIC ISOMERIZATION CATALYST TO FORM 2,7-DIMETHYLNAPHTHALENE IN ADMIXTURE WITH 1,7-DIMETHYLNAPHTHALENE, 2,7DIMETHYLNAPHTHALENE IS RECOVERED FROM THE ISOMERIZATION PRODUCT, E.G. BY CRYSTALLIZATION, AND PART OF THE GENERATED HYDROGEN IS RECYCLED IN THE SYSTEM. THE PROCESS CAN BE VARIED IN SEVERAL WAYS, INCLUDING THE UTILIZATION OF A LIQUID ACIDIC CATALYST IN EITHER THE FIRST STEP OR THE ISOMERIZATION STEP.

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