Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J3/00—Processes of treating or compounding macromolecular substances
  • C08J3/20—Compounding polymers with additives, e.g. colouring
  • C08J3/203—Solid polymers with solid and/or liquid additives
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
  • C08L91/06—Waxes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2201/00—Foams characterised by the foaming process
  • C08J2201/02—Foams characterised by the foaming process characterised by mechanical pre- or post-treatments
  • C08J2201/024—Preparation or use of a blowing agent concentrate, i.e. masterbatch in a foamable composition
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2391/00—Characterised by the use of oils, fats or waxes; Derivatives thereof
  • C08J2391/06—Waxes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2423/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2491/00—Characterised by the use of oils, fats or waxes; Derivatives thereof
  • C08J2491/06—Waxes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L2205/00—Polymer mixtures characterised by other features
  • C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group

Definitions

• Temperature-sensitive active ingredient compositions for density reduction in plastics are Temperature-sensitive active ingredient compositions for density reduction in plastics.
• the present invention relates to highly loaded, temperature-sensitive drug compositions containing propellants which result in density reduction in plastics.
• blowing agent masterbatches foamed.
• the blowing agent masterbatches produced in the extrusion process have blowing agent contents in the range from 10 to 75% by weight and often contain, in addition to a polymeric support, a high proportion of polyolefinic waxes, which promote the incorporation process of the agents into the plastic matrix and the most even distribution possible of the blowing agents to care.
• the propellants should be distributed optimally, the formation of the finest possible cell structure is required, the carrier should be optimally compatible with the polymer and, above all, premature foaming in the processing machine should be prevented.
• a cold mix consisting of a suitable polymer support, such as polyethylene, polypropylene or ethylene vinyl acetate copolymer or similar polymers and additionally dispersing aids, such as waxes,
• Fatty acid derivatives, stearates, etc. may be used.
• the disadvantage of these polymer blends is that the critical melt temperature of the blowing agent is easily exceeded by the polymeric fraction and thus the Decomposition temperature of the blowing agent is reached or exceeded.
• the compatibility with different polymers is very limited.
• JP 10212372 describes the production of an expandable masterbatch which consists of a tack-free polymer which is produced by a catalyst.
• the catalyst used may be a group 4 catalyst.
• the proportion of expandable microsphere products used was 30%.
• Blowing agent concentrates based on polymers whose melting point is above 149 ° C.
• the object of the present invention was to be able to load propellant-containing active ingredient compositions for polymer processing with a very high proportion of different blowing agents, so that the production of foamed plastomers and elastomers can be accomplished economically and ecologically advantageous with a uniform drug composition or preparation and so products of high quality supplies.
• a polymeric support should be largely eliminated, which are on the one hand preparations with a significantly higher active substance content possible and on the other these in significantly more different polymers, with different chemical composition than before, can be used because less compatibility problems due to the high load available.
• the wax carrier should also allow easier incorporation and dispersion into the polymers, resulting in a finer cell structure or a more uniform molecular or molecular weight distribution.
• This object is achieved according to the invention by incorporating the blowing agent components into a metallocene wax or a mixture of metallocene wax with Ziegler wax or a wax polymer mixture.
• the main constituent of the wax carrier is a metallocene wax.
• Metallocene waxes or metallocene polyolefin waxes are by definition waxes prepared in the presence of metallocenes as a catalyst. The composition thus prepared is compounded by extrusion into the active ingredient composition of the invention.
• the present invention thus provides an active substance composition or preparation of the type mentioned at the outset comprising i) one or more finely divided blowing agents, ii) one or more metallocene polyolefin waxes, iii) optionally one or more waxes selected from polar and nonpolar non-metallocene waxes.
• the wax content contains at least 50% by weight of polypropylene metallocene wax, based on the weight of the wax fraction.
• the active compound composition according to the invention thus has a particularly high propellant and filler content, has very good compatibility with the starting polymers and largely excludes negative effects on the mechanical properties in the end product.
• the metallocene waxes have a melt viscosity, measured at a temperature of 170 ° C., in the range from 40 to 80,000 mPa ⁇ s, preferably from 45 to 35,000 mPa ⁇ s, particularly preferably from 50 to 10,000 mPa ⁇ s.
• All waxy components of the active ingredient composition melt in the temperature range between 80 and 170 0 C.
• Preferred active ingredient compositions according to the invention contain from 5 to 90% by weight, preferably from 25 to 85% by weight, of an organic or inorganic propellant and from 7 to 80% by weight, preferably from 7.5 to
• the preparation according to the invention also contains fillers or additives in an amount of from 0 to 30% by weight, based on the total weight of the composition.
• the waxes prepared as catalyst in the presence of metallocene are preferably copolymer waxes of propylene and 0.1 to 50% of ethylene and / or 0.1 to 50% of at least one branched or unbranched 1-alkene having 4 to 20 C atoms with a dropping point ( Ring / ball) between 80 and 170 0 C.
• metallocene waxes prepared in the presence of metallocene as a catalyst are largely or completely amorphous and may additionally be polar modified as needed.
• at least 80 wt%, preferably at least 90 wt%, particularly preferably at least 95 wt%, especially at least 99 wt%, are largely for the purposes of the invention.
• non-metallocene polyolefin waxes on the one hand, ethylene vinyl acetate in particular waxes having a dropping point between 90 and 12O 0 C, a vinyl acetate content of 1 to 30% and a viscosity of 50 to 3,000 mPa-s, preferably from 50 to 1 500 mPa-s , measured at a temperature of 140 0 C, as well as nonpolar, but also polar non-metallocene waxes having a dropping point in the range of 90 to 12O 0 C and a viscosity of less than 30,000 mPa-s, preferably less than 15,000 mPa-s, measured at a temperature of 140 0 C, suitable.
• Suitable non-metallocene polyolefin waxes are homopolymers of ethylene or higher 1-olefins having 3 to 10 carbon atoms or copolymers thereof with one another.
• the polyolefin waxes preferably have a weight-average molar mass M w of between 1000 and 20 000 g / mol and a number-average molar mass M n of between 500 and 15 000 g / mol.
• Metallocene compounds of the formula I are used for the preparation of the metallocene polyolefin waxes used according to the invention.
• This formula also includes compounds of the formula Ia, the formula Ib and the formula Ic
• M 1 is a Group IVb, Vb or VIb metal of the Periodic Table, for example, titanium, zirconium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten, preferably titanium, zirconium, hafnium.
• R 1 and R 2 are identical or different and denote a hydrogen atom, a C 1 -C 10 -O , preferably C 1 -C 5 -alkyl group, in particular methyl, a C 1 -C 10 -, preferably C 1 -C 8 -alkoxy group, a C 6 -C 5 10 , preferably C 6 -C 8 -aryl, a Ce-C 1O -, preferably C 3 -C 8 -aryloxy, a C 2 -C 10, preferably C 2 -C 4 -alkenyl, a C 7 -C 40 -, preferably C 7 -C 0 arylalkyl group, a C 7 -C 4O -, preferably C 7 -C 2 alkylaryl group, a C 8 -C 40 -, preferably C 8 -C 12 -arylalkenyl group or a halogen, preferably chlorine atom.
• R 3 and R 4 are identical or different and denote a mononuclear or polynuclear hydrocarbon radical which can form a sandwich structure with the central atom M 1 .
• R 3 and R 4 are preferably cyclopentadienyl, indenyl, tetrahydroindenyl, benzoindenyl or fluorenyl, it being possible for the basic units to carry additional substituents or to bridge them with one another.
• one of the radicals R 3 and R 4 may be a substituted nitrogen atom, wherein R 24 has the meaning of R 17 and is preferably methyl, tert-butyl or cyclohexyl.
• R 5 , R 6 , R 7 , R 8 , R 9 and R 10 are identical or different and denote a hydrogen atom, a halogen atom, preferably a fluorine, chlorine or bromine atom, a Ci-C 10 -, preferably Ci-C 4 alkyl group, a C 6 -C 0 -, preferably Cs-C 8 -aryl group, a C1-C10, preferably Ci-C 3 alkoxy group, a -NR 1 V, -SR 16 -, -OSiR 1 V, -SiR 1 V or -PR 16 2 radical in which R 15 is a Ci-Ci 0 -, preferably Ci-C 3 alkyl group or Ce-Ci 0 , preferably C 6 -C 8 -aryl group or in the case Si or P also containing radicals is a halogen atom, preferably chlorine atom or two adjacent radicals R 5 , R 6 , R 7 , R 8 , R
• R is 13 CR19, O
• R 17, R 18 and R 19 are identical or different and are a hydrogen atom, a halogen atom, preferably a fluorine, chlorine or bromine atom, a Ci-C 30 -, preferably Ci-C 4 -Alkyk especially methyl group, a Ci- Ci 0 -Fluoralkyl, preferably CF 3 group, a C ⁇ -Cio-Fluoraryl-, preferably pentafluorophenyl, a C 6 -Ci 0 -, preferably Ce-C ⁇ -aryl group, a C 1 -C 0 -, preferably Ci-C 4 alkoxy, in particular methoxy group, a C2-C 10, preferably C 2 -C 4 alkenyl
• M 2 is silicon, germanium or tin, preferably silicon and germanium.
• R 11 and R 12 are the same or different and have the meaning given for R 17 , m and n are the same or different and are zero, 1 or 2, preferably zero or 1, where m plus n is zero, 1 or 2, preferably zero or 1.
• R 14 and R 15 have the meaning of R 17 and R 18 .
• (Indenyl) zirconium Bis (methylcyclopentadienyl) zirconium dichloride, bis (n-butylcyclopentadienyl) zirconium dichloride, bis (octadecylcyclopentadienyl) zirconium dichloride, bis (pentamethylcyclopentadienyl) zirconium dichloride, bis (trimethylsilylcyclopentadienyl) zirconium dichloride, Biscyclopentadienylzirkoniumdibenzyl, Biscyclopentadienylzirkoniumdimethyl, Bistetrahydroindenylzirkoniumdichlorid, dimethylsilyl- ⁇ -fluorenylcyclopentadienylzirkoniumdichlorid, dimethylsilyl-bis-1- (2,3 > 5-trimethylcyclopentadienyl) zirconium dichloride l Dimethylsilyl-
• Suitable cocatalysts for metallocenes of the formula I are organoaluminum compounds, in particular aluminoxanes or else aluminum-free systems such as R 20 x NH 4 - ⁇ BR 21 4, R 20 x PH 4 - x BR 21 4, R 20 3 CBR 21 4 or BR 2 V
• x is a number from 1 to 4
• the radicals R 20 are identical or different, preferably identical, and are C 1 -C 10 -alkyl or C 3 -C 8 -aryl or two radicals R 20 together with the atom connecting them a ring
• the radicals R 21 are the same or different, preferably the same, and are C 6 -C 18 -aryl which may be substituted by alkyl, haloalkyl or fluorine.
• R 20 is ethyl, propyl, butyl or phenyl and R 21 is phenyl, pentafluorophenyl, 3,5-bis-trifluoromethylphenyl, mesityl, xylyl or ToIyI.
• organoaluminum compound e.g. Triethylaluminum, tributylaluminum and others and mixtures suitable.
• supported single-center catalysts can also be used. Preference is given to catalyst systems in which the residual contents of support material and cocatalyst do not exceed a concentration of 100 ppm in the product.
• melt viscosities were determined according to DIN 53019 with a rotary viscometer, the dropping points according to DIN 51801/2, the softening points ring / ball according to DIN EN 1427.
• the drop point determination is carried out with a drop point device according to Ubbelohde according to DIN 51801/2, the softening point ring / ball according to DIN EN 1427.
• compositions according to the invention may additionally contain fillers such as silicates, silicic acids, zeolites, such as
• adjuvants such as antistatic agents, stearates, antioxidants, slip agents and / or Suspension stabilizers, colorants, flame retardants, antiblocking agents, potash and alkaline earth oxides.
• blowing agents examples include azodicarbonamides, nitroso compounds, hydrazides and citric acid as well as citric acid derivatives, salts and esters, sodium bicarbonate or mixtures thereof.
• modified azodicarbonamides which are azodicarbonamides in combination with kickers, such as ZnO, zinc stearate, or Bietsalzen.
• kickers such as ZnO, zinc stearate, or Bietsalzen.
• kickers such as ZnO, zinc stearate, or Bietsalzen.
• organic substances such as acids and bases are also possible.
• Other exothermic blowing agents would be 4,4'-oxybis
• blowing agents are low-boiling liquids such as isopentane or isooctane, and filled with gases or low-boiling liquids microspheres with polymeric shell.
• the required proportion of metallocene waxes depends on the additive-matrix exchange reaction, on the surface structure of the blowing agent, on the surface structure of the finished article, on the desired cell structure, on the starting temperature (degassing temperature) of the blowing agent used and on the desired final product input quantity.
• the present invention also relates to a method for producing the inventive composition by combining the individual components and subsequent homogenization in the extruder or kneader.
• the premixing of the individual components is preferred in the preparation of the composition and can be carried out in a suitable mixing apparatus.
• other additives can be added later via a side dosing in solid or liquid form
• the raw materials used can be in various forms.
• the waxes, as well as the other additives and additives can eg as Granules, dandruff, powder or ultrafine powder may be included in the mixture, while the blowing agents may also be present in liquid form.
• All components can be mixed cold and added via the main feed of an extruder or the waxy / polymeric formulation portions are fed through the main feeder of the extruder, the powdered or liquid propellants are introduced into the machine via respective side feeders. Subsequently, a melt mixture can be carried out in a suitable extruder or in kneaders. This is followed by granulation, grinding or spraying.
• a cold mixture consists of suitable polymer supports, such as polyethylene, polypropylene or ethylene vinyl acetate.
• suitable polymer supports such as polyethylene, polypropylene or ethylene vinyl acetate.
• the disadvantage of such polymer blends is the often limited compatibility of individual components, which can lead to a separation of polymer and the additives such as the blowing agents.
• the heat energy can be introduced via friction, via separate heating of the mixing trough or in both ways.
• the composition on the extruder it is preferable to work with a screw assembly which is tailored to the high active ingredient content.
• the temperature profile is preferably lower than indicated in the prior art.
• Strand granulation is advantageously used for the production of the compositions according to the invention, but underwater granulation or hot blasting can also be used.
• the inventive compositions lead to a reduction in density in partially synthetic or synthetic polymers and are therefore used in particular for the production of foamed plastics or plastic articles.
• polymers can be foamed with the inventive product.
• examples include: polyolefins and copolymers of PE, polyvinyl chloride (PVC) as rigid PVC or as plasticized PVC, ethylene-vinyl acetate copolymers (EVA), polystyrene (PS), styrene-acrylonitrile copolymers (SAN), acrylonitrile Butadiene-styrene copolymers (ABS), polyethylene-ethylene glycol terephthalate (PET), poly-butylene glycol terephthalate (PBT) and their copolyesters, polycarbonate (PC), rubber, butyl rubber, bitumen and blends such as PC / ABS (acrylonitrile-styrene Acrylate terpolymer), PC / PBT or PC / ASA and PMMA (polymethyl methacrylate), as well as thermoplastic polyurethane
• the plastic mixtures can then be further processed to the desired end products.
• a metallocene wax or a metallocene wax mixture prepared from the metallocene PP waxes, polar or nonpolar non-metallocene PE waxes and copolymers of the
• polyolefins a) -d) used according to the invention and listed in Table 1 were obtained by copolymerization of propylene with ethylene with the
• Metallocene catalyst Dimethylsilylbisindenylzirkoniumdichlorid according to the method specified in EP-A-O 384 264 (general instructions Examples 1 to 16). The different softening points and viscosities were adjusted by varying the ethylene input and the polymerization temperature.
• the application is carried out in fine-grained state (sprayed or ground), but granular form is also possible (with separate addition of the individual components to the machine).
• compositions according to the invention were prepared as described below: As a mixture for the extrusion:
• Cooling mixture to 20 - 30 0 C.
• Mixture had an average grain size of less than 1 mm.
• the active compound compositions according to Preparation Examples 1 to 4 were cold-adjusted and used in a co-rotating twin-screw with a low temperature image in different polymers to reduce their density. As a result, a homogeneous foam structure was observed, while at the same time no adverse effect on the mechanical properties of the polymers by the use of the preparations was found.

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• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
• Processes Of Treating Macromolecular Substances (AREA)

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• 2006
  • 2006-09-30 DE DE102006046566A patent/DE102006046566A1/de not_active Withdrawn
• 2007
  • 2007-09-26 JP JP2009529598A patent/JP5412284B2/ja not_active Expired - Fee Related
  • 2007-09-26 WO PCT/EP2007/008366 patent/WO2008037445A1/de not_active Ceased
  • 2007-09-26 ES ES07818450.4T patent/ES2534768T3/es active Active
  • 2007-09-26 US US12/443,398 patent/US8158690B2/en active Active
  • 2007-09-26 HU HUE07818450A patent/HUE025431T2/en unknown
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