Patent Application
20230272200
The present invention relates to a polymer composition comprising a polypropylene, an ethylene based elastomer, a grafted polypropylene and glass fiber. The present invention further relates to a process for the preparation of said polymer composition and to an article comprising the said polymer composition, the present invention further relates to the use of the polymer composition in an article.
Antenna housings are used in antenna stations to provide protection on antennas from the environment. Therefore, it is desirable that the antenna housings are made of polymer compositions with sufficient stiffness and high low temperature impact resistance to withstand extreme weathers, e.g. gale or hail. Another common requirement on the polymer compositions to be used in antenna housing is excellent flowability as the pieces of antenna housing are usually large and prepared by injection molding where excellent flowability is crucial to have the polymer composition fully filled the mold during the injection molding process. Measurement methods of flowability are known in the art, e.g. melt flow index (MFI) measurement and spiral flow measurement. In the context of the present invention, excellent flowability refers to excellent result in spiral flow measurement because spiral flow measurement represents better the flowability than MFI measurement under the injection molding condition.
Antenna housings based polymer compositions comprising polypropylene are known in the art, for instance:
EP 1852938 B1 discloses an antenna housing comprising an electromagnetic window portion through which electromagnetic signals are passed in use, wherein a layer of a wall of the electromagnetic window is formed from self reinforced polypropylene.
US 20170190884 A1 discloses a resin composition for a radar cover. The resin composition includes carbon nanotubes and a polymer resin. The resin composition does not interfere with the transmission of signals from a radar while protecting the radar from the surroundings.
There is still a need to provide a polymer composition with excellent spiral flow performance and falling weight impact resistance at low temperature.
This need is satisfied in the present invention by a polymer composition comprising a polypropylene, an ethylene based elastomer, a grafted polypropylene and glass fiber, wherein the polypropylene has a melt flow index (MFI) in the range from 17 to 68 dg/min as measured according to ISO1133-1:2011 at 230° C./2.16 kg, wherein the amount of the ethylene based elastomer is in the range from 15.5 to 28.3 wt% based on the total amount of the polymer composition, wherein the MFI of the ethylene based elastomer is in the range of 0.8 to 36 dg/min as measured according to ISO1133-1:2011 at 190° C./2.16 kg wherein amount of grafted polypropylene is in the range from 1.2 to 2.9 wt% based on the total amount of the polymer composition.
The inventors of the present invention surprisingly found that the composition according to the invention has excellent spiral flow performance and falling weight impact resistance at low temperature.
The polypropylene according to the invention is preferably a heterophasic propylene copolymer, wherein the heterophasic propylene copolymer may be prepared in one or more reactors, by polymerization of propylene in the presence of a catalyst and optionally subsequent polymerization of an ethylene-α-olefin mixture.
The polypropylene according to present invention can be produced using any conventional technique known to the skilled person, for example multistage process polymerization, such as bulk polymerization, gas phase polymerization, slurry polymerization, solution polymerization or any combinations thereof. Any conventional catalyst systems, for example, Ziegler-Natta or metallocene may be used. Such techniques and catalysts are described, for example, in WO06/010414; Polypropylene and other Polyolefins, by Ser van der Ven, Studies in Polymer Science 7, Elsevier 1990; WO06/010414, US4399054 and US4472524. Preferably, the polypropylene is made using Ziegler-Natta catalyst.
Preferably the polypropylene according to the invention comprises a propylene-based matrix and a dispersed ethylene-α-olefin copolymer.
Preferably the amount of the propylene-based matrix is from 60 to 99 wt%, for example from 65 to 95 wt%, for example from 70 to 90 wt%, for example from 75 to 85 wt%, for example from 72 to 87 wt% based on the total amount of the polypropylene.
Preferably the amount of the dispersed ethylene-α-olefin copolymer is from 40 to 1 wt%, for example from 35 to 5 wt%, for example from 30 to 10 wt%, for example from 28 to 13 wt%, based on the total amount of the polypropylene.
The total amount of the propylene-based matrix and the dispersed ethylene-α-olefin copolymer is preferably 100 wt%. The amount ratio between the propylene-based matrix and the dispersed ethylene-α-olefin copolymer is preferably in the range from 95:5 to 65:35, preferably from 90:10 to 70:30, preferably from 87:13 to 72:28.
The amounts of the propylene-based matrix and the dispersed ethylene-α-olefin copolymer may be determined by NMR, as well known in the art.
The propylene-based matrix may consists of a propylene homopolymer and/or a propylene- α-olefin copolymer consisting of at least 70 wt% of propylene and up to 30 wt% of ethylene and/or an α-olefin having 4 to 10 carbon atoms, for example a propylene- α-olefin copolymer consisting of at least 80 wt% of propylene and up to 20 wt% of ethylene and/or an α-olefin having 4 to 10 carbon atoms, for example consisting of at least 90 wt% of propylene and up to 10 wt% of ethylene and/or an α-olefin having 4 to 10 carbon atoms, based on the total amount of the propylene-based matrix.
The α-olefin in the propylene- α-olefin copolymer may be selected from the group ethylene and α-olefins having 4-10 carbon atoms, for example 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexen, 1-heptene, 1-octene and mixtures thereof, preferably the α-olefin in the propylene- α-olefin copolymer is ethylene.
Preferably, the propylene-based matrix is a propylene homopolymer.
The propylene-based matrix is preferably semi-crystalline, that is it is not 100% amorphous, nor is it 100% crystalline. For example, the propylene-based matrix is at least 40% crystalline, for example at least 50%, for example at least 60% crystalline and/or for example at most 80% crystalline, for example at most 70% crystalline. For example, the propylene-based matrix has a crystallinity of 60 to 70%. For purpose of the invention, the degree of crystallinity of the propylene-based matrix is measured using differential scanning calorimetry (DSC) according to ISO11357-1 and ISO11357-3 of 1997, using a scan rate of 10° C./min, a sample of 5 mg and the second heating curve using as a theoretical standard for a 100% crystalline material 207.1 J/g.
The amount of ethylene in the ethylene-α-olefin copolymer is preferably in the range from 20 to 80 wt% based on the ethylene-α-olefin copolymer, more preferably, the amount of ethylene in the ethylene-α-olefin copolymer is from 30 to 70 wt%, more preferably from 40 to 65 wt%, more preferably from 50 to 65 wt%, even more preferably from 55 to 65 wt%.
Preferably, the α-olefin in the ethylene-α-olefin copolymer is propylene.
The MFI of the polypropylene is in the range from 17 to 68 dg/min, preferably in the range from 23 to 59 dg/min, more preferably in the range from 32 to 47 dg/min as measured according to ISO1133 (2.16 kg/230° C.).
The amount of the polypropylene is preferably in the range from 26 to 76 wt%, preferably in the range from 33 to 62 wt%, more preferably in the range from 39 to 53 wt% based on the total amount of the polymer composition.
In general, glass fiber is a glassy cylindrical substance where its length is significantly longer than the diameter of its cross section. It is known that adding glass fibers is able to improve the mechanical performance (e.g. strength and stiffness) of polymeric resin. The level of performance improvement depends heavily on the properties of the glass fibers, e.g. diameter, length and surface property of the glass fiber.
For the purpose of the present invention, the diameter of the glass fibers is preferably in the range from 5 to 50 microns, preferable from 10 to 30 microns, more preferable from 15 to 25 microns.
It is also know that long glass fiber (length from 0.5 to 50 mm) is able to provide superior property improvement than short glass fiber (length shorter than 0.5 mm) to the composition. The length of glass fibers in the present invention depends heavily on the process used to prepare the said composition. Preferably the glass fiber in the polymer composition according to the invention are long glass fibers.
In the present invention, the amount of glass fibers is preferably in the range from 16 to 42 wt%, preferably in the range from 25 to 34 wt% based on the total amount of the polymer composition.
The polymer composition in the present invention further comprises an ethylene based elastomer.
The ethylene based elastomer is preferably selected from a group consisting of ethylene-butene copolymer, ethylene-hexene copolymer, ethylene-octene copolymer and mixtures thereof, preferably the polyolefin based elastomer is an ethylene-octene copolymer.
Preferably the density of the ethylene based elastomer is preferably in the range from 0.845 to 0.883 g/cm3, preferably in the range from 0.848 to 0.865 g/cm3, more preferably in the range from 0.853 to 0.860 g/cm3 as measured according to ASTM D792-13.
The MFI of the ethylene based elastomer is in the range from 0.8 to 36 dg/min, preferably in the range from 0.9 to 23 dg/min, more preferably in the range from 0.9 to 13 dg/min, even more preferably in the range from 0.9 to 4.8 dg/minas measured according to ISO1133-1:2011 at 190° C./2.16 kg.
The shore A hardness of the ethylene based elastomer is preferably in the range from 35 to 90, preferably in the range from 42 to 69, more preferably in the range from 47 to 60, most preferably in the range from 50 to 57 as measured according to ASTM D2240-15, 1 s..
Ethylene based elastomers which are suitable for use in the current invention are commercially available for example under the trademark EXACT™ available from Exxon Chemical Company of Houston, Texas or under the trademark ENGAGE™ polymers, a line of metallocene catalyzed plastomers available from Dow Chemical Company of Midland, Michigan or under the trademark TAFMER™ available from MITSUI Chemicals Group of Minato Tokyo or under the trademark Fortify™ and Cohere™ from SABIC.
The ethylene based elastomers may be prepared using methods known in the art, for example by using a single site catalyst, i.e., a catalyst the transition metal components of which is an organometallic compound and at least one ligand of which has a cyclopentadienyl anion structure through which such ligand bondingly coordinates to the transition metal cation. This type of catalyst is also known as “metallocene” catalyst. Metallocene catalysts are for example described in U.S. Pat. Nos. 5,017,714 and 5,324,820. The elastomer s may also be prepared using traditional types of heterogeneous multi-sited Ziegler-Natta catalysts.
Preferably, the amount of ethylene incorporated into the polyolefin based elastomer is at least 40 wt%. More preferably, the amount of ethylene incorporated into the polyolefin based elastomer is at least 42 wt%, for example at least 44 wt%. The amount of ethylene incorporated into the polyolefin based elastomer may typically be at most 95 wt%, for example at most 85 wt%, for example at most 75 wt%, for example at most 65 wt%, for example at most 60 wt%, for example at most 58 wt%.
The amount of the ethylene based elastomer is in the range from 15.5 to 28.3 wt%, more preferably in the range from 18.2 to 23.6 wt% based on the total amount of the polymer composition.
When at least part of the hydrogen atoms on the main chain of a polypropylene are substituted by a functional group, the polypropylene becomes a grafted polypropylene.
The grafted polypropylene in the present application is preferably a maleic anhydride grafted polypropylene. Preferably the grafted polypropylene comprises from 0.1 to 3.0 wt.% of maleic anhydride functionalities based on the total amount of the grafted polypropylene.
Maleic anhydride grafted polypropylenes are known in the art and for example available from ExxonMobil under the trade name Exxelor™ PO1015 and Exxelor™ PO1020.
It is preferred that the grafted polypropylene is (semi) crystalline.
The MFI of the grafted polypropylene is preferably in the range from 150 to 600 dg/min, more preferably in the range from 290 to 460 dg/min as measured according to ISO1133-1:2011 at 230° C./2.16 kg.
The amount of the grafted polypropylene is in the range from 1.2 to 2.9 wt% based on the total amount of the polymer composition. The inventor of the present application surprisingly found this amount of grafted polypropylene leads to improved falling weight resistance at low temperature.
The polymer composition may contain the usual additives, for instance nucleating agents and clarifiers, stabilizers, release agents, peroxides, plasticizers, anti-oxidants, lubricants, antistatics, cross linking agents, scratch resistance agents, flame retardants, blowing agents, acid scavengers, recycling additives, anti-microbials, anti-fogging additives, slip additives, antiblocking additives, polymer processing aids and the like. Such additives are well known in the art. The skilled person will know how to choose the type and amount of additives such that they do not detrimentally influence the aimed properties.
The present invention further relates to a process for the preparation of the polymer composition.
The polymer composition according to the invention can be prepared by a process known in the art for the preparation of a fiber reinforced composition, for instance: a pultrusion process, a wire-coating process as described in EP 0921919 B1 and EP 0994978 B1, or compounding. The polymer composition prepared in such process is in pellet form.
The present invention further relates to an antenna housing comprising the polymer composition according to the invention, the amount of the polymer composition is at least 95 wt%, preferably at least 98 wt%, more preferably 100 wt% of the total amount of the antenna housing.
The present invention further relates to a process for the preparation of an antenna housing comprising the following sequential steps:
The present invention further relates to the use of the polymer composition according to the invention in an antenna housing.
Heterophasic propylene copolymer 1 (HECO 1) used for the preparation of samples is commercially available from Sinopec. HECO 1 has an MFI of 35 dg/min as measured according to ISO1133-1:2011 at 230° C./2.16 kg. HECO 1 consist of a propylene homopolymer as matrix and an ethylene-propylene copolymer as dispersed phase, the amount of the dispersed phase in HECO 1 is 16 wt% based on the total amount of HECO 1, the amount of moieties derived from ethylene is 8 wt% based on the total amount of HECO 1.
Heterophasic propylene copolymer 2 (HECO 2) used for the preparation of samples is commercially available from SABIC. HECO 2 has an MFI of 70 dg/min as measured according to ISO1133-1:2011 at 230° C./2.16 kg. HECO1 consist of a propylene homopolymer as matrix and an ethylene-propylene copolymer as dispersed phase, the amount of the dispersed phase in HECO 2 is 17.2 wt% based on the total amount of HECO 2, the amount of moieties derived from ethylene is 7.8 wt% based on the total amount of HECO 2.
Exxelor PO1020 (PO1020) is a maleic anhydride grafted polypropylene commercially available from ExxonMobil. It has a MFI of 430 dg/min as measured according to ISO1133-1:2011 at 230° C./2.16 kg
Several ethylene based elastomer were used in the example, there commercial names, supplier and properties can be found in the table below.
The stabilizers used in the examples is 3.1 wt%. The impregnating agent used in the examples is the same as the one used in WO2009/080281A1, the amount of the impregnating agent is 2.65 wt%. The amounts of additives and the impregnating agent are based on the total amount of the composition.
The glass fibres used were standard Type 30 roving SE4220, supplied by 3B as a roving package, have filament diameter of 19 microns and contain aminosilane-containing sizing composition.
In a first step, HECO was melt-mixed with POE, stabilizers to prepare a thermoplastic resin in pellet form.
In a second step, polymer compositions were prepared by wire-coating process as described in the examples of WO2009/080281A1 using the thermoplastic resin obtained in the first step, glass fibers and impregnating agent. The compositional detail of the polymer compositions is given in Table 2.
In a third step, the pellets of the polymer compositions were injection molded into plaques. The dimensions of the plaques are suitable for the measurements.
Spiral flow: Sprial flow measurements were carried out on a FANUC UH1000, the pellets obtained in the second step of the process were injected with an injection speed of 30 mm/s into a spiral shaped mould and the injection process ended when the pressure of the injection reached 700 kgf/cm2. After the melt cooled down, it was taken out from the mold and its length was measured. The spiral shaped mold’s channel has a rectangular shape cross section with height of 2 mm and width of 15 mm.
Plaques used in this measurement are with dimensions: 830*400*3 mm.
The falling weight impact test was performed on a customized machine. The customized machine comprises two parts: A weight release mechanism and a plaque support.
The weight release mechanism is able to release a metallic ball with 500 gram weight and 50 mm diameter from 2 or 1.3 m height with 0 initial velocity as a free falling object to create falling weight impact on the test plaque.
The plaque support has a square shape with one space in the centre, the outside dimension of the support is 830*400 mm and inside dimension of the dimension is 810*380 mm. The horizontal geometric centre of the outer square superposes with that of the inner square. A plaque was placed horizontally on the plaque support, the horizontal geometric centre of the plaque superposed with that of the support.
The weight release mechanism and the plaque support are positioned in a way that the falling weight impact is created perpendicularly on the plaque surface. The horizontal geometric centre of the plaque superposes with that of the impact point.
The plaque was conditioned in a freezer at -40° C. for at least 4 hours before installation on the plaque support. The whole falling impact operation is completed within 30 secs starting from taking the plaque out of the freezer.
After the falling impact, the plaque was checked visually whether a crack is present on its surface. 5 plaques were tested for each formulation and a non-crack (pass) percentage was calculated.
According to Table 2 IE1 and EX1, a POE amount of higher than 15.5 wt% leads to a clear higher pass rate of falling weight impact test. Comparing IE2 and EX4, a HECO having an MFI in the range of 17 to 68 dg/min as measured according to ISO1133-1:2011 at 230° C./2.16 kg leads to a higher pass rate of falling weigh impact test. The comparison between IE2, EX2 and EX3 shows that POE1 having a MFI in the range from 0.8 to 36 dg/min as measured according to ISO1133-1:2011 at 190° C./2.16 kg leads to improved spiral flow and falling weight impact resistance at low temperature. The comparison between IE2 and EX5 shows that PO1020 in an amount is in the range from 1.2 to 2.9 wt% leads to improved falling weight impact resistance at low temperature.
| Number | Date | Country | Kind |
|---|---|---|---|
| PCT/CN2020/098921 | Jun 2020 | WO | international |
| 20198829.2 | Sep 2020 | EP | regional |
This application is a National Stage application of PCT/EP2021/067668, filed Jun. 28, 2021, which claims the benefit of European Application No. 20198829.2, filed Sep. 28, 2020, and PCT Application PCT/CN2020/098921, filed Jun. 29, 2020, all of which are incorporated by reference in their entirety herein.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2021/067668 | 6/28/2021 | WO |
