DE2257730A1 - THERMOPLASTIC COMPOSITION - Google Patents
THERMOPLASTIC COMPOSITIONInfo
- Publication number
- DE2257730A1 DE2257730A1 DE19722257730 DE2257730A DE2257730A1 DE 2257730 A1 DE2257730 A1 DE 2257730A1 DE 19722257730 DE19722257730 DE 19722257730 DE 2257730 A DE2257730 A DE 2257730A DE 2257730 A1 DE2257730 A1 DE 2257730A1
- Authority
- DE
- Germany
- Prior art keywords
- carboxylic acid
- metal salt
- acid
- free carboxylic
- free
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 229920001169 thermoplastic Polymers 0.000 title claims description 11
- 239000004416 thermosoftening plastic Substances 0.000 title claims description 11
- 239000000203 mixture Substances 0.000 title claims description 9
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 21
- 229910052751 metal Inorganic materials 0.000 claims description 18
- 239000002184 metal Substances 0.000 claims description 18
- 239000002253 acid Substances 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 15
- -1 polyethylene Polymers 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000004698 Polyethylene Substances 0.000 claims description 6
- 229920000573 polyethylene Polymers 0.000 claims description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 5
- 229920000098 polyolefin Polymers 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 238000000354 decomposition reaction Methods 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 230000015556 catabolic process Effects 0.000 description 14
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 11
- 238000006731 degradation reaction Methods 0.000 description 10
- 235000021355 Stearic acid Nutrition 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 6
- 239000008117 stearic acid Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000002843 carboxylic acid group Chemical group 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- ZVEWFTICTSQBDM-UHFFFAOYSA-N 4-methylphenol Chemical compound [CH2]C1=CC=C(O)C=C1 ZVEWFTICTSQBDM-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241000711981 Sais Species 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 235000021152 breakfast Nutrition 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical compound O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 150000002505 iron Chemical class 0.000 description 1
- XHQSLVIGPHXVAK-UHFFFAOYSA-K iron(3+);octadecanoate Chemical compound [Fe+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XHQSLVIGPHXVAK-UHFFFAOYSA-K 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- SZINCDDYCOIOJQ-UHFFFAOYSA-L manganese(2+);octadecanoate Chemical compound [Mn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O SZINCDDYCOIOJQ-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- IWDCLRJOBJJRNH-UHFFFAOYSA-N para-hydroxytoluene Natural products CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000013502 plastic waste Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005629 polypropylene homopolymer Polymers 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
PATENTANWÄLTE DR -ING. H. FlNCKEPATENT LAWYERS DR -ING. H. FlNCKE
DIPL.-ING.H BOHR lh. NOV. 1972 DIPL.-ING.H BOHR lh. NOV. 1972
MÖNCHEN 5 MOLLERSTR. 31MÖNCHEN 5 MOLLERSTR. 31
Imperial Chemical Induetries Limited, London,Imperial Chemical Induetries Limited, London,
Grossbritannien !EhermoplastiaessönGreat Britain! Ehermoplastiaessön
Die Erfindung betrifft Xhermoplastmassen.The invention relates to xhermoplastic compositions.
Die Verwendung wegirerfbarer Verpackungen, Behalter undThe use of disposable packaging, containers and
309822/11309822/11
dergleichen und das absichtliche oder versehentliche Wegwerfen dieser Gegenstände aus Kunststoff hat das Problem des Kunststoffabfalls hervorgerufen. Die Verwendung der erfindungsgemässen Kunstetoffmassen kann diese Schwierigkeiten verringern.the like and the deliberate or accidental throwing away of these plastic items has that Plastic waste problem caused. The use of the plastic compositions according to the invention can alleviate these difficulties.
Erfindungsgemess enthält eine Thermoplastmasse als Abbauhllfsitittel eine freie Carbonsäure und ein Metallsalz einer Carbonsäure, wobei das Metall eine Atomzahl von 22 bis 29 hat und wobei diese beiden Komponenten in einer solchen Menge vorhanden sind, dassAccording to the invention contains a thermoplastic material as A free carboxylic acid and a decomposition aid Metal salt of a carboxylic acid, the metal having an atomic number of 22 to 29 and both of these Components are present in such an amount that
(a) die Gesamtmenge an Metallsalz und freier Carbonsäure zwischen 0,001 und 40 Gev% der Gesamtmasse ausmacht, und dass(a) the total amount of metal salt and free carboxylic acid between 0.001 and 40% by weight of the total mass matters and that
(b) die Menge an freier Carbonsäure 10 bis 95 Gew%, vorzugsweise 50 bis 90 Gew%, bezogen auf die Gesamtmenge an Metallsalz und freier Carbonsäure beträgt.(b) the amount of free carboxylic acid 10 to 95% by weight, preferably 50 to 90% by weight, based on the Total amount of metal salt and free carboxylic acid.
Die Metalle mit Atomzahlen von 22 bis 29 sind Ti, T1 Cr, Mn, Fe, Co, Ni und Cu. Unter diesen werden die Metalle Eisen und Mangan bevorzugt.The metals with atomic numbers from 22 to 29 are Ti, T 1 Cr, Mn, Fe, Co, Ni and Cu. Among these, the metals iron and manganese are preferred.
Die beschriebenen Thermoplastmassen umfassen sowohlThe thermoplastic compositions described include both
- 3 309822/1100 - 3 309822/1100
gebrauchsfertige Hassen ale auch Eonsentrat©, d.h. hochkonzentrierte Massen, die dem reinen Polymer unter Bildung einer gebrauchsfertigen Hasse zugegeben warden können. Bei den gebrauchsfertigen Massen bötragt die Konzentration (a) meistens 0,01 bis 2%, vorzugsweise 0,1 bis 1%. Die Masse kann eine einseines Polymer oder eine Polymermischung enthalten»ready-to-use hats ale also Eonsentrat ©, i.e. highly concentrated masses that are underneath the pure polymer Formation of a ready-made hatred may be added can. In the case of the ready-to-use masses, the Concentration (a) mostly 0.01 to 2%, preferably 0.1 to 1%. The mass can be a single polymer or contain a polymer mixture »
Die freie Carbonsäure entspricht vorzugsweise aber nicht unbedingt dem verwendeten Carbonsäuremetallsalze In beiden Fällen ist die Carbonsäure vorzugsweise eine solche mit der Formel R.COOH, worin R eine Kohlenwasserstoff gruppe mit bis zu 30 Kohlenstoffatomen darstellt. In Frage kommen als Säuren insbesondere diejenigen, bei denen R ein geradkettige Kohlenwasserstoff gruppe mit 8 bis 21 Kohlenstoffatomen und mit weniger als 3 Doppelbindungen darstellt.The free carboxylic acid preferably, but not necessarily, corresponds to the carboxylic acid metal salt In used In both cases, the carboxylic acid is preferably one with the formula R.COOH, where R is a hydrocarbon represents a group with up to 30 carbon atoms. Particularly suitable acids are those in which R is a straight-chain hydrocarbon group with 8 to 21 carbon atoms and with represents less than 3 double bonds.
Das Abbauhilfsmittel nach der Erfindung eignet sich zur Beschleunigung der Abbaugeschwindigkeit von insbesondere Olefinpolymeren, Copolymeren aus Olefinen und anderen damit copolymerisierbaren Monomeren sowie Mischungen aus Olefinpolymeren und/odes? -copolymeren»The degradation aid according to the invention is suitable to accelerate the rate of degradation of, in particular, olefin polymers, copolymers of olefins and other monomers copolymerizable therewith as well as mixtures of olefin polymers and / odes? -copolymers »
Bevorzugte Olefinpolymere sind:Preferred olefin polymers are:
- 4 - . 309822/1100 - 4 -. 309822/1100
O) Homopolymere aus Äthylen, Propylen, Buten-1, 4-Methylpenten-i und Styrol;O) homopolymers of ethylene, propylene, butene-1, 4-methylpentene-i and styrene;
(2) Copolymere aus den obigen Monomeren miteinander sowie mit anderen a-Olefinen.(2) Copolymers of the above monomers with each other as well as with other α-olefins.
Die bevorzugten Olefincopolymere bestehen aus solchen, die mindestens 50 Gew% Äthylen, Propylen, Buten-1, 4-Methylpenten-t und/oder Styrol zusammen mit mindestens einem der folgenden Comonomeren einpolymerisiert enthalten:The preferred olefin copolymers consist of those which contain at least 50% by weight of ethylene, propylene, butene-1, 4-methylpentene-t and / or styrene together with at least contain one of the following comonomers in copolymerized form:
Die bevorzugten Olefin-Copolymere unfassen auch die Ionomere, die durch Neutralisierung oder teilweise Neutralisierung der Carbonsäuregruppen derjenigen Copolymere, die Carbonsauregruppen enthalten, hergestellt werden.The preferred olefin copolymers also include those Ionomers obtained by neutralizing or partially neutralizing the carboxylic acid groups of those Copolymers containing carboxylic acid groups are prepared.
309822/1100309822/1100
Copolymere, die mindestens 50 Gew% Äthylen einpolymerisiert enthalten, sind besonders zweckmässig.Copolymers in which at least 50% by weight of ethylene are polymerized are particularly useful.
Ausser dem Polymer und dem Abbauhilfsmittel kann eine Hasse nach der Erfindung auch andere für Thermoplast« massen übliche Zusatzstoffe enthalten. Bei Polyolefinen können die Hassen z.B. Antiblockingmittel, Gleitmittel, Stabilisatoren zur Stabilisierung der Hasse bei deren Verarbeitung sowie Stabilisatoren ott Stabilisierung der Hasse im Gebrauch (d.h. nach der Verarbeitung) enthalten.In addition to the polymer and the decomposition aid, one hater according to the invention can also use others for thermoplastic « contain a lot of common additives. With polyolefins Can the haters e.g. antiblocking agents, lubricants, stabilizers to stabilize the haters at theirs Processing and stabilizers ott stabilization the hate included in use (i.e. after processing).
Die Erfindung betrifft Verpackungsmaterialien, Bindfäden und Behälter (auch Behälterdeckel) aus der definitionsgemässen Kunststoffmasse. Als Behälter kommen z.B. Beutel, Säcke, Schachtelf Kartons* Flaschen, Parfümbeutel, Tassen und Patronenhülsen in Frage.The invention relates to packaging materials, string and containers (including container lids) made from the plastic compound as defined. Possible containers are, for example, bags, sacks, boxes for cardboard boxes, bottles, perfume bags, cups and cartridge cases.
Auch betrifft die Erfindung einen Verkaufsgegenstand, der in einem Material aus einer Kunststoffmasse nach der Erfindung verpackt ist.The invention also relates to an object of sale which is packaged in a material made of a plastic compound according to the invention.
Im folgenden werden mehrere Hassen nach der Erfindung beispielsweise näher beschrieben. Xn allen Beispielen wurden pulverförmiges £isen(III)st©arat und ein® pulverförmige Carbonsäure oder ein® flussige CarbonsäureIn the following, several hats according to the invention are described in more detail, for example. In all examples, pulverulent isene (III) stearate and a pulverulent carboxylic acid or a liquid carboxylic acid were used
- 6 309822/1100 - 6 309822/1100
gelost in einem Alkohol (in einigen Fällen auch ein Antioxydans) mit Polyäthylen gemahlen. Nach Herstellung der Mischung wurde 10 Minuten weiter gemahlen, um ein Walzenfell herzustellen. Das Valzenfell wurde bei einer geeigneten Temperatur zwischen Folien,aus Polyethylenterephthalat unter Bildung eines 125 pm dicken zusammenhängenden Films gepresst. Yon diesem Film wurden Proben mit den Abmessungen 1 χ 5 cm abgeschnitten und in der FS/BL-Früfung geprüft.dissolved in an alcohol (in some cases also an antioxidant) ground with polyethylene. After the mixture was prepared, milling was continued for 10 minutes to produce a milled sheet. The Valzenfell was pressed between sheets of polyethylene terephthalate at a suitable temperature to form a continuous film 125 μm thick. Samples measuring 1 × 5 cm were cut from this film and tested in the FS / BL test.
Die Proben wurden mit UV-Strahlen von einer Kombination aus gleichen Anzahlen von 20-Watt-Fluoreszenzsonnenlampen und 20-Watt-Schwarzlampen bestrahlt. Die Proben kreisten um die Lampen in einem Anstand Ton 10 cm von den Lampen, um eine gleichmässige Bestrahlung zu erreichen. Die Proben wurden täglich untersucht und auf Bissbildung beim Biegen geprüft. Die Zeit bis zu einem positiven Ergebnis bei dieser Prüfung zeigt die Wirksamkeit des Abbauhilfsmittels an, wobei eine kürzere Zeit ein wirksameres Abbauhilfsmittel andeutet.The samples were exposed to UV rays from a combination of equal numbers of 20 watt fluorescent sun lamps and 20 watt black lamps irradiated. The samples circled around the lamps in a propriety Sound 10 cm from the lamps in order to achieve even irradiation. The rehearsals were daily examined and checked for bite formation when bending. The time to a positive result with this one Testing indicates the effectiveness of the breakdown aid, with a shorter time being a more effective breakdown aid indicates.
In der Tabelle 1 sind die Versprödungszeiten bei derTable 1 shows the embrittlement times for
- 7 -309822/1100- 7 -309822/1100
FS/BL-Prüfung an Proben aus Hochdruckpolyäthylen nit den angegebenen Mengen an EiBen(XII)stearat (Metallsalz) und freier Stearinsäure in Tagen angegeben· In der Tabelle sind ausserdem die Ergebnisse beim Prüfen von Proben, die zusätzlich 0,02 Gew% BHT (eine übliche Bezeichnung für das Antioxydans 2,6-Di-tert. -butyl-4»methylphenol) enthalten, angegeben.FS / BL test on samples made of high pressure polyethylene nit the specified amounts of egg (XII) stearate (metal salt) and free stearic acid in days The table also shows the results for Testing samples that additionally contain 0.02% by weight BHT (a common name for the antioxidant 2,6-di-tert. -butyl-4 »methylphenol) are given.
Gew%Free acid
Weight%
Saure imAcid im
Gesamttotal
abbaudegradation
mittelmiddle
0,02 Gew%
BHTwith
0.02 wt%
BHT
hilfsmittel
6ev%Total degradation
tools
6ev%
BHTwithout
BHT
Gew%!
Weight%
0,0080.008
Der Kbntrollversuch (d.h. an Hochdruckpolyäthjlen ohne Zusätze) ergab eine Versprödungszeit von 23 Tagen.The control test (i.e. on high-pressure polyethylene without additives) showed an embrittlement time of 23 days.
In der Tabelle 2 sind entsprechende Ergebnisse Niederdruckpolyäthylen mit den angegebenen Hengen an Eisen(III)stearat (Hetallsalz) und freier Stearinsäure aufgeführt. Table 2 shows the corresponding results of low-pressure polyethylene with the specified amounts of iron (III) stearate (metal salt) and free stearic acid.
... 8 309822/1100 ... 8 309822/1100
hilfsmittel Säure imauxiliary acid im
- ' Geeemtn. >- 'Geeemtn. >
Die vier Ergebnisse bei 0,2* Gesamtabbauhilsmittel zeigen, dass sowohl die Saure als auch das SaIs als Abbauhilfsmittel wirksam sind, dass die beiden zusammen aber eine erhöhte Wirkung haben»The four results at 0.2 * total breakdown aid show that both the acid and the SaIs are effective as breakdown agents that the two together but have an increased effect »
In der Tabelle 3 sind die Ergebniese aufgeführt, die bei der Zugabe verschiedener anderer Säuren zum gleichen Grundgemisch erhalten werden. In allen Fällen enthält das Gemisch:Table 3 shows the results that when various other acids are added to the same basic mixture. In all In some cases the mixture contains:
. 9 -309822/1100. 9 -309822/1100
0,08 Gew% £isen(IIX)stearat 0,02 Gew# Stearinsäure0.08 wt% isene (IIX) stearate 0.02 wt # stearic acid
0,1 Gew% andere Säure (wie angegeben) (d.h. 0,2 Gew% Gesamtabbauhilfsmittel und freie Säure bezogen auf das Gessmtaibbauhilfsmittel)0.1 wt% other acid (as indicated) (i.e. 0.2 wt% total degradation aid and free acid based on the bulk building aid)
enthaltend1 double bond
containing
enthaltend2 double bonds
containing
Der Tabelle 3 ist wohl zu entnehmen, dass die A^t des Radikals B in den Sauren der Formel E. COOH, worin E ein lohlenwaeserstoffreäikal darstallt 9 die Abbau-» geschwindigkeit nicht wesentlich beeinflusst«From Table 3 it can be seen that the A ^ t of the radical B in the acids of the formula E. COOH, in which E is a hydrogen free radical 9 "does not significantly influence" the rate of degradation.
Eine Prüfung des Abbaue von Hanganstearat als AbbauhilfsmittelAn examination of the degradation of hangan stearate as a degradation aid
309822/11309822/11
Bei einem Gehalt von 0,6 Gew% Manganstearat und 1 Gew% Stearinsäure (d.h. einem Gehalt von 1,6 GeiM% Gesamt* abbauhilfsmittel, wovon 62% aus Säure bestanden) betrug die Lebensdauer 2 Tage nach dem FS/KL-iest. Ohne Saure betrug die Lebensdauer 9 Tage. Bei Verwendung des Manganetearats wurde das Polyäthylen weniger gefärbt als bei Verwendung des Eisensalzes.With a content of 0.6 wt% manganese stearate and 1 wt% Stearic acid (i.e. a content of 1.6% total * degradation aids, of which 62% consisted of acid) the service life 2 days after the FS / KL-iest. Without acid the lifespan was 9 days. When using the Manganetearats made the polyethylene less colored than when using the iron salt.
Die den Abbau fördende Wirkung der synergistischen Kombination aus 0,08 Gew% £isen(III)stearat und 0,02 Gew% Stearinsäure ist der Tabelle 4 zu entnehmen, in der die Ergebnisse der obigen Prüfung an einer Reihe von Thermoplasten angegeben sind.The degradation-promoting effect of the synergistic Combination of 0.08% by weight isen (III) stearate and 0.02% by weight of stearic acid can be found in Table 4, in which the results of the above test on a number of thermoplastics are given.
Thermoplast Lebensdauer in Tagen.Thermoplastic lifetime in days.
mit Abbau- ohne Abbaumittel mittelwith dismantling agent without dismantling agent
7,5% Vinylacetat/Ithylen ♦ Polypropylenhomopolymer ·* SOHLYU®A 1555 ♦·· 7.5% vinyl acetate / ethylene ♦ Polypropylene homopolymer · * SOHLYU®A 1555 ♦ ··
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309822/1100309822/1100
Schmelsindex.2,0. Dichte 0,926 g/cm^. Der film wurde auf eine Starke von 125 μια gepresst»Schmelsindex 2.0. Density 0.926 g / cm ^. The film was pressed to a thickness of 125 μια »
*♦ Das Polypropylen wurde mit 0,1 % 0,1 % 2,6-Di-tert. ->butyl»4-methylphenol ©tabilieiert und su eine Schlauchfolie mit einer Starke von 20 \m bei 2200C geblasen.* ♦ The polypropylene was 0.1 % 0.1% 2,6-di-tert. -> butyl "4-methyl phenol © tabilieiert and below a tubular film with a strong 20 \ m blown at 220 0 C.
*** Ein teilweise neutralisiertes Copolymer aus Äthylen und Methacrylsäure, das zu einer Folie mit einer Starke von 125 \m gepresst wurde«*** A partially neutralized copolymer of ethylene and methacrylic acid that has been pressed into a film having a strength of 125 \ m '
- 12 309822/1100- 12 309822/1100
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5456671A GB1401418A (en) | 1971-11-24 | 1971-11-24 | Plastics composition |
Publications (1)
Publication Number | Publication Date |
---|---|
DE2257730A1 true DE2257730A1 (en) | 1973-05-30 |
Family
ID=10471438
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19722257730 Ceased DE2257730A1 (en) | 1971-11-24 | 1972-11-24 | THERMOPLASTIC COMPOSITION |
Country Status (9)
Country | Link |
---|---|
JP (1) | JPS568053B2 (en) |
AU (1) | AU473461B2 (en) |
BE (1) | BE791912A (en) |
CA (1) | CA1090498A (en) |
DE (1) | DE2257730A1 (en) |
FR (1) | FR2160945B1 (en) |
GB (1) | GB1401418A (en) |
NL (1) | NL7215159A (en) |
SE (1) | SE396084B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2455732A1 (en) * | 1973-11-28 | 1975-06-05 | Coloroll Ltd | BIODEGRADABLE MASS |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5136783B2 (en) * | 1972-03-29 | 1976-10-12 | ||
IT1178605B (en) * | 1984-10-31 | 1987-09-09 | Fiocchi Munizioni Spa | HUNTING, SHOOTING AND SIMILAR COMPONENTS IN PHOTODEGRADABLE SYNTHETIC PLASTIC MATERIAL |
WO1986005871A1 (en) * | 1985-03-27 | 1986-10-09 | Scientific Cartridge Developments Limited | Shotgun cartridge |
US4780319A (en) * | 1985-07-08 | 1988-10-25 | Merck & Co., Inc. | Organic acids as catalysts for the erosion of polymers |
GB8712009D0 (en) * | 1987-05-21 | 1987-06-24 | Folk Drive Eng Ltd | Degradable plastics |
BE1002431A4 (en) * | 1987-07-07 | 1991-02-05 | Lilaran & Sons Uk Ltd B | In the air biodegradable ethylene polymers. |
GB9108555D0 (en) * | 1991-04-22 | 1991-06-05 | Kent Cartridge Mfg | Improvements in cartridge cases |
FR2741627B1 (en) * | 1995-11-27 | 1997-12-19 | Poudres & Explosifs Ste Nale | FULLY BIODEGRADABLE COMPOSITIONS USEFUL FOR MAKING HUNTING AND SHOOTING CARTRIDGES |
FR2754265B1 (en) * | 1996-10-04 | 1998-12-18 | France Cheddite | COLORED PHOTODEGRADABLE PLASTIC MATERIAL, PIECE SUCH AS SOCKET, PAD AND PROJECTILE, OBTAINED FROM SUCH MATERIAL |
NO324368B1 (en) * | 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. |
GB2464285A (en) * | 2008-10-08 | 2010-04-14 | Wells Plastics Ltd | Transition metal additives for enhancing polymer degradation |
-
0
- BE BE791912D patent/BE791912A/en unknown
-
1971
- 1971-11-24 GB GB5456671A patent/GB1401418A/en not_active Expired
-
1972
- 1972-11-07 AU AU48615/72A patent/AU473461B2/en not_active Expired
- 1972-11-09 NL NL7215159A patent/NL7215159A/xx not_active Application Discontinuation
- 1972-11-22 FR FR7241436A patent/FR2160945B1/fr not_active Expired
- 1972-11-23 CA CA157,334A patent/CA1090498A/en not_active Expired
- 1972-11-23 SE SE1527272A patent/SE396084B/en unknown
- 1972-11-24 JP JP11725372A patent/JPS568053B2/ja not_active Expired
- 1972-11-24 DE DE19722257730 patent/DE2257730A1/en not_active Ceased
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2455732A1 (en) * | 1973-11-28 | 1975-06-05 | Coloroll Ltd | BIODEGRADABLE MASS |
Also Published As
Publication number | Publication date |
---|---|
FR2160945A1 (en) | 1973-07-06 |
JPS568053B2 (en) | 1981-02-21 |
SE396084B (en) | 1977-09-05 |
NL7215159A (en) | 1973-05-28 |
FR2160945B1 (en) | 1978-01-06 |
CA1090498A (en) | 1980-11-25 |
GB1401418A (en) | 1975-07-16 |
AU4861572A (en) | 1974-05-09 |
AU473461B2 (en) | 1976-06-24 |
JPS4864130A (en) | 1973-09-05 |
BE791912A (en) | 1973-05-24 |
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