"> PRODUCTION OF ALPHA-CRYSTAL MODIFICATION OF 2,2',2

    公开(公告)号:JPH1059989A

    公开(公告)日:1998-03-03

    申请号:JP16003697

    申请日:1997-06-17

    Applicant: HOECHST AG

    Abstract: PROBLEM TO BE SOLVED: To obtain the α-crystal modification of a 2,2',2"-nitrilo(triethyltris(3,3',5,5'-tetra-tert-butyl-1,1'-biphenyl- 2,2'-diyl) phosphite) (NTTBP) by dissolving NTTBP in a short-chain ketone in heated condition, and cooling the solution. SOLUTION: This α-crystal modification of a 2,2',2"-nitrilo(triethyltris(3,3',5,5'- tetra-tert-butyl-1,1'-biphenyl-2,2'-diyl) phosphite) (NTTBP) of formula I is obtained by dissolving NTTBP in the formula of its melt, amorphous solid modification or β-crystal modification into a short-chain 3-7C ketone (e.g. acetone) in heated condition at 40-100 deg.C, and then cooling the solution to room temperature to crystallize the α-crystal modification of NTTBP.

    ADDITIVE MIXTURE EXHIBITING NUCLEUS-FORMING ACTION AND USED FOR SYNTHETIC RESIN MATERIAL

    公开(公告)号:JPH1036556A

    公开(公告)日:1998-02-10

    申请号:JP8964297

    申请日:1997-04-08

    Applicant: HOECHST AG

    Abstract: PROBLEM TO BE SOLVED: To obtain the subject new additive mixture capable of remarkably reducing the release of the decomposition products of dibenzylidene sorbitol or its derivative, when its mixture of a polymer is processed, by adding an amide functional compound to the dibenzylidene sorbitol or its derivative. SOLUTION: This additive mixture comprises (A) dibenzylidene sorbitol or its derivative [preferably 1,3:2,4-di(benzylidene)-D-sorbitol, etc.,] and (B) an amide functional compound (preferably bisstearoyl ethylenediamine, bislauroyl ethylenediamine, etc.,) preferably in a B:A mixing ratio of 1.5:l to 1:1.5 as basic components. When added to a polymer, the objective mixture is preferably added so that the component B is contained in a concentration of 0.1-1wt.% based on the whole amount of the polymer. The polymer to be mixed with the objective mixture includes polyolefins.

    "> PRODUCTION OF 2,2',2

    公开(公告)号:JPH1059988A

    公开(公告)日:1998-03-03

    申请号:JP16003597

    申请日:1997-06-17

    Applicant: HOECHST AG

    Abstract: PROBLEM TO BE SOLVED: To produce a 2,2',2"-nitrilo(triethytris(3,3',5,5'-tetra-tert-butyl-1,1'- biphenyl-2,2'-diyl) phosphite), which is used as a stabilizer for polymers, etc., by making a 6-chloro-tetratert-butylbenzo-dioxaphosphepine with triethanolamine and a tertiary amine react at specific mol ratios. SOLUTION: This 2,2',2"-nitrilo(triethyltris(3,3',5,5'-tetra-tert-butyl-1,1'- biphenyl-2,2'-diyl) phosphite), which is a highly effective stabilizer for polymers, is obtained by adding a 6-chloro-2,4,8,10-tetratert-butylbenzo[d, f][1,3,3]dioxaphosphepine (chlorophophite) of formula I into a solution of triethanolamine and a tertiary amine (e.g. triethylamine) at mol ratios of the chlorophosphite, tertiary amine and triethanolamine of (3.3-2.9):(3.3-2.9):1 to complete the reaction of them, and separating the product from the tertiary amine hydrochloride after the reaction.

    "> Verfahren zur Herstellung der Alpha-Kristall-Modifikation des 2,2',2
    4.
    发明公开
    Verfahren zur Herstellung der Alpha-Kristall-Modifikation des 2,2',2"-Nitrilo-¬triethyl-tris(3,3',5,5'-tetra-tert.-butyl-1,1'biphenyl-2,2'-diyl)phosphits 失效
    Verfahren zur Herstellung der Alpha-Kristall-Modifikation des 2,2',2“ - 三 - 三乙基 - 三(3,3',5,5'-四叔丁基-1,1'-联苯-2, 2'-二基)次磷盐

    公开(公告)号:EP0814085A1

    公开(公告)日:1997-12-29

    申请号:EP97109379

    申请日:1997-06-10

    Applicant: HOECHST AG

    CPC classification number: C07F9/65746

    Abstract: Die vorliegende Erfindung bezieht sich auf ein Verfahren zur Herstellung der α-Kristall-Modifikation des 2,2',2''-Nitrilo[triethyl-tris(3,3',5,5'-tetra-tert.-butyl-1,1'-biphenyl-2,2'-diyl)phosphits] (abgekürzt NTTBP) der Formel worin man das NTTBP in Form seiner Schmelze, seiner amorphen Festphasenmodifikation oder seiner β-Kristall-Modifikation in kurzkettigen Ketonen mit 3 bis 7 C-Atomen wie Methylethylketon oder insbesondere Aceton in der Wärme bei 40 bis 100°C löst und anschließend durch Abkühlen auf Raumtemperatur zur Kristallisation bringt.

    Abstract translation: 制备式(I)化合物的α-晶体改性的方法包括以其熔体形式溶解(I),或者将无定形固相改性或β-晶态改性溶解在3- 7C短链酮(II)在40-100℃下,然后通过冷却至室温结晶。

    6.
    发明专利
    未知

    公开(公告)号:DE59207976D1

    公开(公告)日:1997-03-13

    申请号:DE59207976

    申请日:1992-07-24

    Applicant: HOECHST AG

    Abstract: Aryl diarylphosphinites of the formula (I) … … where n = 1 or 2, and in which R and R , independently of one another, are, as monovalent radicals, phenyl or naphthyl, each of which may carry from 1 to 5 substituents, the substituents being identical or different and being nonaromatic hydrocarbon radicals, alkoxy radicals, alkylthio radicals or dialkylamino radicals, each having 1 to 8 carbon atoms, aryl or aryloxy, each having 6 to 10 carbon atoms, or halogen having an atomic number of 9 to 35, and R as a divalent radical, is phenylene or biphenylene which is unsubstituted or substituted by up to 4 nonaromatic hydrocarbon radicals having 1 to 8 carbon atoms, or is naphthylene which is unsubstituted or substituted by 1 to 4 nonaromatic hydrocarbon radicals having 1 to 8 carbon atoms as substituents, and R , R and R , independently of one another, are hydrogen or branched or unbranched hydrocarbon radicals having 1 to 8 carbon atoms. … The invention furthermore relates to a process for the preparation of the compounds of the formula (I) and to the use thereof for the stabilisation of plastics, in particular plastics obtained by polymerisation.

    9.
    发明专利
    未知

    公开(公告)号:DE59008284D1

    公开(公告)日:1995-03-02

    申请号:DE59008284

    申请日:1990-07-07

    Applicant: HOECHST AG

    Abstract: In polyphenylene ethers, in particular polyphenylene sulphide, the addition of a small amount of an organophosphorus compound of the formula II, III or IV retards crystallisation and reduces the crystallisation temperature in the melt.

    10.
    发明专利
    未知

    公开(公告)号:DE3940572A1

    公开(公告)日:1991-06-20

    申请号:DE3940572

    申请日:1989-12-08

    Applicant: HOECHST AG

    Abstract: By dividing the known condensation of acetoacetic acid diol esters with phenols into two process steps, a reduction in the cost of the entire process can be achieved. Methyl acetoacetate is first condensed with a phenol and the methyl 3,3-bis(4-hydroxyalkylphenyl)butanoate formed is reacted with the desired diol in the presence of a transesterification catalyst. In this way only one acetoacetic ester is necessary for various final products. The final products are useful stabilizers for plastics, in particular polyolefins.

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