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  • 类似技术
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    • 专利摘要:
    1519529 Photo-degradable polymer compositions SOC CHIMIQUE DES CHARBONNAGES 15 April 1976 [17 April 1975] 15686/76 Heading C3K Polymers of ethylene and styrene are rendered photo-degradable by the incorporation therein of a salt of iron (II) with a carboxylic acid which has an alkyl group containing at least 6 carbon atoms and having an alkyl chain which has at position 2, 3, 4 or 5 relative to the carboxylic group at position 1, a second carboxylic, sulphonic acid, alcohol or amide group. Compounds exemplified are the iron salts of dodecylsuccinic acid, O-palmitoyl-l-ascorbic acid, O- palmitoyl gluconic acid, N-palmitoyl diiminoacetic acid, N-palmitoyl glutamic acid, monostearyl succinic acid and monolaurylethanolamido sulphosuccinic acid. The compositions may also contain sulphur.
    公开号:SU764613A3
    申请号:SU762351804
    申请日:1976-04-16
    公开日:1980-09-15
    发明作者:Нику Женевьев
    申请人:Сосьете Шимик Де Шарбоннаж (Фирма)；
    IPC主号:
    专利说明:

    This invention relates to a degradable polymer composition comprising at least a polymer and a ferrous salt. The known polymer composition, including polyethylene or ethylene / vinyl acetate copolymer, includes salts or complexes as additives to polymers for the preparation of photodegradable RZ polymer compositions. However, the known additives are not effective enough. The object of the invention is the acceleration of destruction. The goal is achieved by the fact that a polymer: a composition containing polyethylene or a copolymer of ethylene with vinyl acetate and a photodestructive additive contains, as a last resort, a ferrous iron salt selected from the group including iron (II) dodecyl succinate, iron (II), iron 6.0-palmitoyl ascorbate iron (N ), Iron (II) 1,0-palmitoylgluconate, iron N-palmitoyldiiminoacetate (I and iron (II) monostearyl sulfosuccinate, with the following ratio of components, parts by weight, polyethylene or ethylene-vinyl acetate copolymer 100, organic salt dvuhvale 0.001-0.02. Polymer compositions used according to the invention may contain other known additives, such as antioxidants, plasticizers. Salts of ferrous iron, used according to the invention, are well-known products. when the corresponding acid is protected against air, freshly prepared ferrous carbonate or by double decomposition in air of an acid salt (e.g., potassium salt) with iron alum. Acids, if necessary, can be obtained by exposing the acid chloride to the hydroxy acid or hydroxy acid in the pyridine medium. All of these ferrous salts have particularly interesting properties as additives according to the invention. They are compatible with polymers and are easily dispersed in polymers due to the long alkyl chain they contain.
    They do not possess thermodestructive action in c. polymer ratio. This property is probably due to the presence of an eamestite in V. position 2, 3, 4, or 5, which has a complexing action for iron (II). This substituent is also responsible for the stability, during storage, of the used additives, as well as the appearance of the rancid Odor, caused by lime additives, such as iron (III) salts. :
    They are little toxic or non-toxic. which makes it possible to use the compositions according to the invention in food applications for plastics. They are not capable of being extracted with water. -; ;; -:,,; , -. ,,
     According to the invention, photochemical degradation of the polymer is regulated by adjusting the amount of the added additive. Ops make it possible to conclude that the photochemical degradation of polymers is enhanced under the influence of the additive until the optimum value depends on the molar absorption coefficient of the additive and the thickness of the irradiated object (product), the increase in destructibility is clearly reduced : is.
    The addition of sulfur (in the form of sulfur or polysulfide) in the compositions according to the invention simultaneously with dvuhvatkantny iron allows you to lengthen n; the original photodegradation of polymeric compositions.
    Compositions according to the invention are prepared by mixing, when heated, a polymer with the above or above additives to obtain a homogeneous mixture; To accomplish this operation, you can use the well-known Methods for obtaining homogeneous mixtures based on plastics. . Measures 1-7. The polymer compositions according to the invention are prepared by thoroughly mixing with heating a polyethylene with a bulk weight of 0.92 and a melting index of 1.9 with various additives with bivalent iron and various known cases with different amounts of sulfur, l
    The resulting Composi and Sho are then transformed into a film with a thickness of 500 μm and the substrates are irradiated for a different time in an apparatus for accelerated aging under the action of UV-shielded ATLAS 600 type. . . ..
    Effect of add Estimate; The film obtained, the film, allows you to determine the loss (%) of the length during the decree of the A1H Sample relative to the sample before irradiation. . g ..:
    R e zultat predstv avleny V t abl. one.
    Comparative experiments are carried out in order to emphasize the specific effect of supplements according to
    invention compared with the action of previously known additives.
    For evidence of the effect of an alkyl chain having more than 6 atoms, carbon, 0.01 parts by weight of polyethylene was used to implement examples 1-7. iron salts (I) in the form of gluconate or succinate, the resulting products are irradiated and loss (%) elongation at break of the sample is measured. When irradiated for 213 h with the addition of iron (II) glycrate, the loss was 13%.
     When irradiated for 196 hours with the addition of iron (II) succinate, the loss was 10%.
    In order to show the effect of iron valence in the additive, similar experiments were carried out using 0.01 parts by weight as an additive. iron (III) salts in the form of glycerol phosphate, sodium ferritcitrate or sodium ferritartrate, respectively. After irradiation of the obtained products for 200 hours, the elongation losses at break were 16, 2 and 3%, respectively.
    The resistance to thermal oxidation of polyethylene containing additives according to the invention is very good. This property can be shown by studying the measurement depending on the duration of the calendering at the sample, the melting index of polyethylene from the initial melting index of about 2. Table 2 shows the results obtained:
    for a control sample of polyethylene,
    1 - for the same polyethylene, to which 0.01 parts by weight was added. iron salts in the form of iron (II) dodecyl succinate,
    2-. for the same polyethylene, to which is added 0.01 weight.h. iron salts in the form of 1,0-palmitoyl ascorbate iron (I),
    3- for the same polyethylene to which is added
    0.01 weight.h. iron salts in the form of iron (II) dodecyl succinate and 0.01; weight parts. sulfur,
    4- for the same polyethylene to which is added
    0.01 weight.h. salt-in. in shape. 1.0-palonyl iron sorbate (I () and 0.01 parts by weight of sulfur.
    5- For this: the same polyethylene and to which 0.01-, weight.h. iron (III) salts in the form of tristearate. . V
    Procedures 8 and 9. Repeat aging tests as described in examples 1-7, using ethylene-ninyl acetate copolymer as a polymer substance, containing 6.5% vinylacetate and indexes opal and i, 5. This copolymer does not contain an antioxidant.
    The results obtained are presented in Table 3. .
    PRI me d 10. To show different in the mechanism of action of the Product according to the invention (Example 2A or 2F) and the product of a previously known form (0.01 parts by weight of iron salt (IM) in the form of tripalmitate
    and 0.01 weight.h. sulfur), depending on the duration of exposure to UV rays, the loss of elongation at break, the percentage of oxygen and the weight content of substances extracted by the LBHL in molded plates with a thickness of 500 µm Of polyethylene with a melting index of 2 containing additives. The results are presented in table 4.
    ten
    ; t a b l and c a t
    1A Iron Dodecyl Succinate (M)
    1B Same
    1C
    1D
    2A 1,0-Palmitoyl Iscorbate Iron {I O
    2B Same
    2C
    0.01
    0.01
    0.01
    0.01
    0.01
    0.02
    0.001
    764613
    Continuation of table 1
    table 2
    ascorbate gel of the invention Polymer composition containing polyethylene or ethylene-vinyl acetate copolymer and photo-destructing additive, characterized in that, in order to accelerate the degradation, it contains as a destructive additive an organic salt of bivalent iron selected from the group, selected from the group, which is in the range of the organic salt of the iron, selected from the group, selected from the group, is selected from the group of organic iron salt selected from the group that is in the range of the destructive addition of an organic salt of bivalent iron, selected from the group that is active in the destructiveness of the additive, selected from the group that is active in the organic salt of , 6.0-pshmitamoilascorbate iron (II), 1,0-palmitoylgluconate
    T a b l and c a
    iron (II), N-palmitoyl diiminoacetate iron (II) and monostearyl iron sulfosuccinate (M), in the following ratio of components, parts by weight: polyethylene or copolymer
    40 ethylene with vinyl acetate 100, organic ferrous salt 0.001-0.02.
    Sources of information taken into account in the examination
    45 Patent of France 2199757, cl. From 08 27/00, published in 1974.
    权利要求:
    Claims (1)
    [1]
    The invention contains a polymer composition containing polyethylene or a copolymer of ethylene with vinyl acetate and a photodestructive additive, characterized in that, in order to accelerate the destruction, it contains an organic divalent iron salt selected from the group comprising iron (II) dodecylsuccinate, as a destructive additive, 6, Iron (II) O-palmitoyl ascorbate, 1, Iron (I) O-palmitoyl gluconate, Iron (II) N-palmitoyldiiminoacetate and iron (II) monostearyl • sulfosuccinate, in the following ratio, parts by weight: polyethylene and whether a copolymer of 40 ethylene with vinyl acetate 100, an organic salt of ferrous iron 0.001-0.02.
    类似技术:
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    同族专利:
    公开号 | 公开日
    NL7604109A|1976-10-19|
    CA1072803A|1980-03-04|
    EG12747A|1979-09-30|
    HU174388B|1979-12-28|
    IT1070334B|1985-03-29|
    FR2307840A1|1976-11-12|
    US4028480A|1977-06-07|
    DK171376A|1976-10-18|
    JPS5946267B2|1984-11-12|
    IE42678L|1976-10-17|
    BG27912A3|1980-01-15|
    DE2616257A1|1976-10-28|
    IE42678B1|1980-09-24|
    FR2307840B1|1977-09-23|
    LU74781A1|1977-01-12|
    GR58452B|1977-10-10|
    BE840883A|1976-08-16|
    GB1519529A|1978-08-02|
    JPS51133342A|1976-11-19|
    BR7602328A|1976-10-12|
    引用文献:
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    GB1356107A|1970-07-22|1974-06-12|Scott G|Polymer compositions|
    GB1342622A|1971-02-19|1974-01-03|Ici Ltd|Plastics composition|
    US3830764A|1972-07-06|1974-08-20|Princeton Polymer Lab|Degradable hydrocarbon polymers|
    FR2199757A5|1972-09-20|1974-04-12|Ethylene Plastique Sa|US4520155A|1984-04-23|1985-05-28|The Lubrizol Corporation|Dye-receptive polyolefins and polyolefin fibers|
    DE3844179A1|1988-12-29|1990-07-05|Hoechst Ag|DEGRADABLE POLYMER BLOCKS|
    JP3128787B2|1990-04-10|2001-01-29|凸版印刷株式会社|Polyolefin resin sheet having oxygen barrier properties and oxygen barrier container|
    US5518730A|1992-06-03|1996-05-21|Fuisz Technologies Ltd.|Biodegradable controlled release flash flow melt-spun delivery system|
    NO324368B1|2003-04-23|2007-10-01|Normors As|Process for preparing additive for thermoplastics and such prepared additive as well as thermoplastics containing such additive.|
    US8343710B1|2005-03-11|2013-01-01|The Regents Of The University Of Colorado, A Body Corporate|Photodegradable groups for tunable polymeric materials|
    US9180196B2|2005-03-11|2015-11-10|The Regents Of The University Of Colorado, A Body Corporate|Photodegradable groups for tunable polymeric materials|
    CN104311956B|2014-10-14|2016-07-13|蚌埠天成包装材料有限公司|A kind of hygroscopic film material for citric acid agglomeration resistance packaging|
    CN108250562B|2016-12-29|2021-02-02|武汉金发科技有限公司|Low-odor low-emission polypropylene composite material and preparation method thereof|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    FR7512000A|FR2307840B1|1975-04-17|1975-04-17|
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