Process for preparing 1,3-propanediol
    1.
    发明授权
    Process for preparing 1,3-propanediol 失效
    1,3-丙二醇制备方法

    公开(公告)号:US5463145A

    公开(公告)日:1995-10-31

    申请号:US316673

    申请日:1994-09-30

    摘要: 1,3-Propanediol is prepared in a process comprising the steps of:contacting, in an essentially non-water-miscible organic solvent, ethylene oxide with carbon monoxide and hydrogen in the presence of a catalytic amount of a non-phosphine-ligated cobalt compound and an effective amount of a lipophilic quaternary phosphonium salt promoter at a temperature within the range of about 50.degree. to about 100.degree. C. and a pressure within the range of about 500 to about 5000 psig, to produce an intermediate product mixture comprising less than 15 wt % 3-hydroxypropanal;adding an aqueous liquid to said intermediate product mixture and extracting into said aqueous liquid a major portion of the 3-hydroxypropanal at a temperature less than about 100.degree. C. to provide an aqueous phase comprising 3-hydroxypropanal in greater concentration than the concentration of 3-hydroxypropanal in the intermediate product mixture, and an organic phase comprising at least a portion of the cobalt compound and at least a portion of the lipophilic quaternary phosphonium salt;contacting the aqueous phase comprising 3-hydroxypropanal with hydrogen in the presence of a hydrogenation catalyst at a pressure of at least about 100 psig and a temperature during at least a portion of the hydrogenation step of at least 40.degree. C. to provide a hydrogenation product mixture comprising 1,3-propanediol.

    摘要翻译: 以包括以下步骤的方法制备1,3-丙二醇:在催化量的非磷化氢连接的钴存在下,在基本上与水可混溶的有机溶剂中,使环氧乙烷与一氧化碳和氢气接触 化合物和有效量的亲脂性季鏻盐助催化剂,其温度范围为约50至约100℃,压力范围为约500至约5000psig,以产生包含较少量的中间产物混合物 超过15重量%的3-羟基丙醛; 向所述中间产物混合物中加入水性液体并在低于约100℃的温度下将3-羟基丙醛的主要部分提取到所述水性液体中,以提供比3-浓度更高的浓度的3-羟基丙醛的水相 - 羟基丙醛,以及包含至少一部分钴化合物和至少一部分亲脂性季鏻盐的有机相; 在氢化催化剂的存在下,在至少约100psig的压力和在至少40℃的至少一部分氢化步骤期间的温度下使包含3-羟基丙醛的水相与氢气接触以提供氢化产物 混合物包含1,3-丙二醇。

    Cobalt-catalyzed process for preparing 1,3-propanediol using a
lipophilic dihydroxyarene promoter
    2.
    发明授权
    Cobalt-catalyzed process for preparing 1,3-propanediol using a lipophilic dihydroxyarene promoter 失效
    使用亲脂性二羟基芳烃助催化剂制备1,3-丙二醇的钴催化方法

    公开(公告)号:US5576471A

    公开(公告)日:1996-11-19

    申请号:US316669

    申请日:1994-09-30

    摘要: 1,3-Propanediol is prepared in a process which involves reacting ethylene oxide with carbon monoxide and hydrogen in an essentially non-water-miscible solvent in the presence of a non-phosphine-ligated cobalt catalyst and a lipophilic dihydroxyarene promoter to produce an intermediate product mixture containing 3-hydroxypropanal in an amount less than 15 wt %; extracting the 3-hydroxypropanal from the intermediate product mixture into an aqueous liquid at a temperature less than about 100.degree. C. and separating the aqueous phase containing 3-hydroxypropanal from the organic phase containing cobalt catalyst; hydrogenating the 3-hydroxypropanal in the aqueous phase to 1,3-propanediol; and recovering the 1,3-propanediol.The process enables the production of 1,3-propanediol in high yields and selectivity without the use of a phosphine ligand-modified cobalt catalyst.

    摘要翻译: 1,3-丁二醇的制备方法是在非磷化氢连接的钴催化剂和亲脂性二羟基芳烃助催化剂存在下,使环氧乙烷与一氧化碳和氢气在基本上不与水相混溶的溶剂中进行反应,生成中间体 含有小于15重量%的3-羟基丙醛的产物混合物; 在低于约100℃的温度下将中间产物混合物中的3-羟基丙醛萃取到含水液体中,并从含钴催化剂的有机相中分离出含有3-羟基丙醛的水相; 将水相中的3-羟基丙醛氢化为1,3-丙二醇; 并回收1,3-丙二醇。 该方法能够以高产率和选择性生产1,3-丙二醇,而不需要使用膦配体改性的钴催化剂。

    Cobalt-catalyzed process for preparing 1,3-propanediol using a
lipophilic phosphine oxide promoter
    3.
    发明授权
    Cobalt-catalyzed process for preparing 1,3-propanediol using a lipophilic phosphine oxide promoter 失效
    使用亲脂性氧化膦促进剂制备1,3-丙二醇的钴催化方法

    公开(公告)号:US5563302A

    公开(公告)日:1996-10-08

    申请号:US316680

    申请日:1994-09-30

    摘要: 1,3-Propanediol is prepared in a process which involves reacting ethylene oxide with carbon monoxide and hydrogen in an essentially non-water-miscible solvent in the presence of a non-phosphine-ligated cobalt catalyst and a lipophilic phosphine oxide promoter to produce an intermediate product mixture containing 3-hydroxypropanal in an amount less than 15 wt %; extracting the 3-hydroxypropanal from the intermediate product mixture into an aqueous liquid at a temperature less than about 100.degree. C. and separating the aqueous phase containing 3-hydroxpropanal from the organic phase containing cobalt catalyst; hydrogenating the 3-hydroxypropanal in the aqueous phase to 1,3-propanediol; and recovering the 1,3-propanediol.The process enables the production of 1,3-propanediol in high yields and selectively without the use of a phosphine ligand-modified cobalt catalyst.

    摘要翻译: 在一种方法中制备1,3-丙二醇,该方法包括在非磷化氢连接的钴催化剂和亲脂性氧化膦促进剂的存在下,将环氧乙烷与一氧化碳和氢气在基本上不与水混溶的溶剂中反应,以产生 含有小于15重量%的3-羟基丙醛的中间产物混合物; 在低于约100℃的温度下将中间产物混合物中的3-羟基丙醛萃取到含水液体中,并将​​含有3-羟基丙醛的水相与含钴催化剂的有机相分离; 将水相中的3-羟基丙醛氢化为1,3-丙二醇; 并回收1,3-丙二醇。 该方法能够以高产率和选择性地制备1,3-丙二醇而不使用膦配体改性的钴催化剂。

    Process for preparing 1,3-propanediol
    4.
    发明授权
    Process for preparing 1,3-propanediol 失效
    1,3-丙二醇制备方法

    公开(公告)号:US5545767A

    公开(公告)日:1996-08-13

    申请号:US316679

    申请日:1994-09-30

    摘要: 1,3-propanediol is prepared in a process comprising the steps of:contacting ethylene oxide with carbon monoxide and hydrogen in an essentially non-water-miscible solvent in the presence of an effective amount of a non-phosphine-ligated cobalt catalyst and an effective amount of a lipophilic phenol at a temperature within the range of about 50.degree. to about 100.degree. C. and a pressure within the range of about 500 to about 5000 psig, under reaction conditions effective to produce an intermediate product mixture comprising less than about 15 wt % 3-hydroxypropanal;adding an aqueous liquid to said intermediate product mixture and extracting into said aqueous liquid at a temperature less than about 100.degree. C. a major portion of the 3-hydroxypropanal so as to provide an aqueous phase comprising 3-hydroxypropanal in greater concentration than the concentration of 3-hydroxypropanal in said intermediate product mixture and an organic phase comprising at least a portion of the cobalt catalyst or a cobalt-containing derivative thereof and at least a portion of the lipophilic phenol;contacting the aqueous phase comprising 3-hydroxypropanal with hydrogen in the presence of a hydrogenation catalyst at a pressure of at least about 100 psig and a temperature during at least a portion of the hydrogenation step of at least 40.degree. C. to provide a hydrogenation product mixture comprising 1,3-propanediol.

    摘要翻译: 以包括以下步骤的方法制备1,3-丙二醇:在有效量的非磷化氢连接的钴催化剂存在下,将环氧乙烷与一氧化碳和氢气在基本上不与水相混溶的溶剂中接触, 在约50℃至约100℃的温度范围内的有效量的亲油性苯酚和在约500至约5000psig范围内的压力,在有效产生包含小于约 15重量%3-羟基丙醛; 向所述中间产物混合物中加入水性液体并在小于约100℃的温度下将3-羟基丙醛的主要部分萃取到所述水性液体中,以提供包含比浓度更高的浓度的3-羟基丙醛的水相 所述中间产物混合物中的3-羟基丙醛和包含至少一部分钴催化剂或其含钴衍生物和至少一部分亲脂性酚的有机相; 在氢化催化剂的存在下,在至少约100psig的压力和在至少40℃的至少一部分氢化步骤期间的温度下使包含3-羟基丙醛的水相与氢气接触以提供氢化产物 混合物包含1,3-丙二醇。

    Cobalt-catalyzed process for preparing 1,3-propanediol using a
lipophilic quaternary arsonium salt promoter
    5.
    发明授权
    Cobalt-catalyzed process for preparing 1,3-propanediol using a lipophilic quaternary arsonium salt promoter 失效
    使用亲脂性季铵盐助催化剂制备1,3-丙二醇的钴催化方法

    公开(公告)号:US5545765A

    公开(公告)日:1996-08-13

    申请号:US316661

    申请日:1994-09-30

    摘要: 1,3-Propanediol is prepared in a process which involves reacting ethylene oxide with carbon monoxide and hydrogen in an essentially non-water-miscible solvent in the presence of a non-phosphine-ligated cobalt catalyst and a lipophilic quaternary arsonium salt promoter to produce an intermediate product mixture containing 3-hydroxypropanal in an amount less than 15 wt %; extracting the 3-hydroxypropanal from the intermediate product mixture into an aqueous liquid at a temperature less than about 100.degree. C. and separating the aqueous phase containing 3-hydroxypropanal from the organic phase containing cobalt catalyst; hydrogenating the 3-hydroxypropanal in the aqueous phase to 1,3-propanediol; and recovering the 1,3-propanediol.The process enables the production of 1,3-propanediol in high yields and selectivity without the use of a phosphine ligand-modified cobalt catalyst.

    摘要翻译: 在一种方法中制备1,3-丙二醇,该方法包括在非磷化氢连接的钴催化剂和亲脂性季铵盐助催化剂的存在下,使环氧乙烷与一氧化碳和氢气在基本上不与水相混溶的溶剂中反应,生成 含有小于15重量%的3-羟基丙醛的中间产物混合物; 在低于约100℃的温度下将中间产物混合物中的3-羟基丙醛萃取到含水液体中,并从含钴催化剂的有机相中分离出含有3-羟基丙醛的水相; 将水相中的3-羟基丙醛氢化为1,3-丙二醇; 并回收1,3-丙二醇。 该方法能够以高产率和选择性生产1,3-丙二醇,而不需要使用膦配体改性的钴催化剂。

    Process for preparing 1,3-propanediol
    6.
    发明授权
    Process for preparing 1,3-propanediol 失效
    1,3-丙二醇制备方法

    公开(公告)号:US5463144A

    公开(公告)日:1995-10-31

    申请号:US316671

    申请日:1994-09-30

    摘要: 1,3-propanediol is prepared in a process comprising the steps of:contacting ethylene oxide with carbon monoxide and hydrogen in an essentially non-water-miscible solvent in the presence of an effective amount of a non-phosphine-ligated cobalt catalyst and an effective amount of a lipophilic quaternary ammonium salt at a temperature within the range of about 50.degree. to about 100.degree. C. and a, pressure within the range of about 500 to about 5000 psig, under reaction conditions effective to produce an intermediate product mixture comprising less than 15 wt % 3-hydroxypropanal;adding an aqueous liquid to said intermediate product mixture and extracting into said aqueous liquid at a temperature less than about 100.degree. C. a major portion of the 3-hydroxypropanal so as to provide an aqueous phase comprising 3-hydroxypropanal in greater concentration than the-concentration of 3-hydroxypropanal in said intermediate product mixture and an organic phase comprising at least a portion of the cobalt catalyst or a cobalt-containing derivative thereof and at least a portion of the lipophilic quaternary ammonium salt;contacting the aqueous phase comprising 3-hydroxypropanal with hydrogen in, the presence of a hydrogenation catalyst at a pressure of at least about 100 psig and a temperature during at least a portion of the hydrogenation step of at least 40.degree. C. to provide a hydrogenation product mixture comprising 1,3-propanediol.

    摘要翻译: 以包括以下步骤的方法制备1,3-丙二醇:在有效量的非磷化氢连接的钴催化剂存在下,将环氧乙烷与一氧化碳和氢气在基本上不与水相混溶的溶剂中接触, 在有效量的亲油性季铵盐的温度范围为约50至约100℃,和a,压力范围为约500至约5000psig,在有效产生中间产物混合物的反应条件下,包括 小于15重量%的3-羟基丙醛; 向所述中间产物混合物中加入水性液体,并在低于约100℃的温度下将3-羟基丙醛的主要部分萃取到所述含水液体中,以提供包含比所述中间产物混合物更高浓度的3-羟基丙醛的水相, 所述中间产物混合物中的3-羟基丙醛的浓度和包含至少一部分钴催化剂或其含钴衍生物和至少一部分亲脂性季铵盐的有机相; 在氢化催化剂存在下,在至少约100psig的压力和在至少40℃的至少一部分氢化步骤期间的温度下使包含3-羟基丙醛的水相与氢接触以提供氢化 产物混合物包含1,3-丙二醇。

    Process for preparing 1,3-propanediol
    7.
    发明授权
    Process for preparing 1,3-propanediol 失效
    1,3-丙二醇制备方法

    公开(公告)号:US5463146A

    公开(公告)日:1995-10-31

    申请号:US316677

    申请日:1994-09-30

    摘要: 1,3-propanediol is prepared in a process comprising the steps of:(a) contacting ethylene oxide with carbon monoxide and hydrogen in an essentially non-water-miscible solvent in the presence of an effective amount of a non-phosphine-ligated cobalt catalyst and an effective amount of a lipophilic arsine at a temperature within the range of about 50 to about 100.degree. C. and a pressure within the range of about 500 to about 5000 psig, under reaction conditions effective to produce an intermediate product mixture comprising less than about 15 wt % 3-hydroxypropanal;(b) adding an aqueous liquid to said intermediate product mixture and extracting into said aqueous liquid at a temperature less than about 100.degree. C. a major portion of the 3-hydroxypropanal so as to provide an aqueous phase comprising 3-hydroxypropanal in greater concentration than the concentration of 3-hydroxypropanal in said intermediate product mixture and an organic phase comprising at least a portion of the cobalt catalyst or a cobalt-containing derivative thereof and at least a portion of the lipophilic arsine;(c) separating the aqueous phase from the organic phase;(d) contacting the aqueous phase comprising 3-hydroxypropanal with hydrogen in the presence of a hydrogenation catalyst at a pressure of at least about 100 psig and a temperature during at least a portion of the hydrogenation step of at least 40.degree. C. to provide a hydrogenation product mixture comprising 1,3-propanediol;(e) recovering 1,3-propanediol from said hydrogenation product mixture; and(f) returning at least a portion of the organic phase comprising cobalt compound and lipophilic arsine to the process of step (a).The process enables the production of 1,3-propanediol in high yields and selectivity without the use of a phosphine-ligated cobalt catalyst.

    摘要翻译: 以包括以下步骤的方法制备1,3-丙二醇:(a)在有效量的非磷化氢连接的钴的存在下,将环氧乙烷与一氧化碳和氢气在基本上不与水相混溶的溶剂中接触 催化剂和有效量的亲油胂在约50至约100℃的温度和约500至约5000psig范围内的压力下,在有效产生包含较少的中间产物混合物的反应条件下 比约15重量%的3-羟基丙醛; (b)向所述中间产物混合物中加入含水液体并在低于约100℃的温度下将3-羟基丙醛的主要部分萃取到所述水性液体中,以提供含有更高浓度的3-羟基丙醛的水相 所述中间产物混合物中的3-羟基丙醛的浓度和包含至少一部分钴催化剂或其含钴衍生物和至少一部分亲脂性胂的有机相; (c)将水相与有机相分离; (d)在氢化催化剂的存在下,在至少约100psig的压力和至少一部分氢化步骤的至少40℃的温度下使包含3-羟基丙醛的水相与氢气接触,以提供 包含1,3-丙二醇的氢化产物混合物; (e)从所述氢化产物混合物回收1,3-丙二醇; 和(f)将包含钴化合物和亲脂性胂的至少一部分有机相返回到步骤(a)的方法。 该方法能够以高产率和选择性生产1,3-丙二醇,而不需要使用磷化氢连接的钴催化剂。

    Cobalt-catalyzed process for preparing 1,3-propanediol using a
lipophilic tertiary amine promoter
    8.
    发明授权
    Cobalt-catalyzed process for preparing 1,3-propanediol using a lipophilic tertiary amine promoter 失效
    使用亲脂性叔胺助催化剂制备1,3-丙二醇的钴催化方法

    公开(公告)号:US5585528A

    公开(公告)日:1996-12-17

    申请号:US316660

    申请日:1994-09-30

    摘要: 1,3-Propanediol is prepared in a process which involves reacting ethylene oxide with carbon monoxide and hydrogen in an essentially non-water-miscible solvent in the presence of a non-phosphine-ligated cobalt catalyst and a lipophilic tertiary amine promoter to produce an intermediate product mixture containing 3-hydroxypropanal in an amount less than 15 wt %; extracting the 3-hydroxypropanal from the intermediate product mixture into an aqueous liquid at a temperature less than about 100.degree. C. and separating the aqueous phase containing 3-hydroxypropanal from the organic phase containing cobalt catalyst; hydrogenating the 3-hydroxypropanal in the aqueous phase to 1,3-propanediol; and recovering the 1,3-propanediol.The process enables the production of 1,3-propanediol in high yield and selectivity without the use of a phosphine ligand-modified cobalt catalyst.

    摘要翻译: 在一种方法中制备1,3-丙二醇,该方法包括在非磷化氢连接的钴催化剂和亲脂性叔胺促进剂的存在下,将环氧乙烷与一氧化碳和氢气在基本上不与水相混溶的溶剂中反应,以产生 含有小于15重量%的3-羟基丙醛的中间产物混合物; 在低于约100℃的温度下将中间产物混合物中的3-羟基丙醛萃取到含水液体中,并从含钴催化剂的有机相中分离出含有3-羟基丙醛的水相; 将水相中的3-羟基丙醛氢化为1,3-丙二醇; 并回收1,3-丙二醇。 该方法能够以高产率和选择性生产1,3-丙二醇,而不需要使用膦配位体改性的钴催化剂。

    Process for recycling mixed polymer containing polyethylene terephthalate
    9.
    发明授权
    Process for recycling mixed polymer containing polyethylene terephthalate 失效
    回收含聚对苯二甲酸乙二醇酯的混合聚合物的方法

    公开(公告)号:US5554657A

    公开(公告)日:1996-09-10

    申请号:US436078

    申请日:1995-05-08

    摘要: The invention described herein provides a process for recycling a mixed polymer recycle stream containing polyester polymers, particularly polyethylene terephthalate (PET) typically in the form of carbonated soft drink or other containers. This novel process includes the steps of: (1) contacting the mixed polymer recycle stream with a solvent which selectively dissolves the PET. (2) separating the selective solvent containing PET from the residual mixed polymer, (3) cooling the selective solvent to precipitate the PET, and (4) removing the selective solvent from the precipitated PET. It is preferable that the mixed polymer recycle stream be prepared for recycling by conventional steps, such as water washing. In a preferred embodiment, the mixed polymer recycle stream is chemically washed subsequent to water washing and prior to contact with the selective solvent. The PET recovered is preferably combined with "virgin" PET and further processed to increase its molecular weight.

    摘要翻译: 本文描述的本发明提供了一种用于再循环含有聚酯聚合物,特别是通常为碳酸软饮料或其它容器形式的聚对苯二甲酸乙二醇酯(PET)的混合聚合物再循环料流的方法。 该新方法包括以下步骤:(1)使混合的聚合物再循环流与选择性溶解PET的溶剂接触。 (2)从残留混合聚合物中分离含有选择性溶剂的PET,(3)冷却选择性溶剂使PET沉淀,(4)从析出的PET中除去选择性溶剂。 优选混合聚合物再循环流通过常规步骤如水洗来制备用于再循环。 在优选的实施方案中,混合聚合物再循环料流在水洗后和与选择性溶剂接触之前进行化学洗涤。 回收的PET优选与“原始”PET组合并进一步加工以增加其分子量。

    Cobalt-catalyzed process for preparing 1,3-propanediol using a
lipophilic bidentate phosphine promotor
    10.
    发明授权
    Cobalt-catalyzed process for preparing 1,3-propanediol using a lipophilic bidentate phosphine promotor 失效
    使用亲脂性二齿膦促进剂制备1,3-丙二醇的钴催化方法

    公开(公告)号:US5545766A

    公开(公告)日:1996-08-13

    申请号:US316668

    申请日:1994-09-30

    摘要: 1,3-Propanediol is prepared in a process which involves reacting ethylene oxide with carbon monoxide and hydrogen in an essentially non-water-miscible solvent in the presence of a non-phosphine-ligated cobalt catalyst and a lipophilic bidentate phosphine promoter to produce an intermediate product mixture containing 3-hydroxypropanal in an amount less than 15 wt%; extracting the 3-hydroxypropanal from the intermediate product mixture into an aqueous liquid at a temperature less than about 100.degree. C. and separating the aqueous phase containing 3-hydroxypropanal from the organic phase containing cobalt catalyst; hydrogenating the 3-hydroxypropanal in the aqueous phase to 1,3-propanediol; and recovering the 1,3-propanediol.The process enables the production of 1,3-propanediol in high yield and selectivity without the use of a phosphine ligand-modified cobalt catalyst.

    摘要翻译: 在一种方法中制备1,3-丙二醇,该方法包括在非磷化氢连接的钴催化剂和亲脂性二齿膦催化剂的存在下,将环氧乙烷与一氧化碳和氢气在基本上不与水相混溶的溶剂中反应,以产生 含有小于15重量%的3-羟基丙醛的中间产物混合物; 在低于约100℃的温度下将中间产物混合物中的3-羟基丙醛萃取到含水液体中,并从含钴催化剂的有机相中分离出含有3-羟基丙醛的水相; 将水相中的3-羟基丙醛氢化为1,3-丙二醇; 并回收1,3-丙二醇。 该方法能够以高产率和选择性生产1,3-丙二醇,而不需要使用膦配位体改性的钴催化剂。