Curable composition for use in a high temperature lithography-based photopolymerization process and method of producing crosslinked polymers therefrom
US-2024325117-A1 · Oct 3, 2024 · US
US10138335B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10138335-B2 |
| Application number | US-201515525711-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 17, 2015 |
| Priority date | Nov 19, 2014 |
| Publication date | Nov 27, 2018 |
| Grant date | Nov 27, 2018 |
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Injection molded article for healthcare applications based on propylene homopolymer having a melt flow rate in the range of 40 to 120 g/10 min, a pentad isotacticity of more than 92.5%, and meso sequence length of 91.0 to 160.
Opening claim text (preview).
What is claimed is: 1. Injection molded article comprising a propylene homopolymer having (a) a melt flow rate MFR 2 (230° C./2.16 kg) measured according to ISO 1133 in the range of 40 to 120 g/10 min; (b) a pentad isotacticity (mmmm) of more than 92.5% determined by 13 C-NMR; and (c) a meso sequence length (MSL4) of 91.0 to 160; MSL4 is calculated by formula (1) MSL 4 = 2 * [ mmmm ] [ mmmr ] + 4 ( 1 ) wherein “[mmmm]” is % of mmmm pentads “[mmmr]” is % of mmmr pentads, determined by 13 C-NMR spectroscopy. 2. Injection molded article according to claim 1 , wherein the propylene homopolymer has a meso sequence length (MSL2) of equal to or more than 65.0; MSL2 is calculated by formula (2) MSL 2 = 2 * [ mm ] [ mr ] + 2 ( 2 ) wherein “[mm]” are % of mm triads, “[mr]” are % of mr triads, determined by 13 C-NMR spectroscopy. 3. Injection molded article according to claim 1 , wherein the propylene homopolymer has (a) a triad syndiotacticity (rr) of not more than 2.5% as determined by 13 C-NMR spectroscopy; and/or (b) a pentad isotacticity (mmmm) of more than 92.5 to 97.3% as determined by 13 C-NMR spectroscopy. 4. Injection molded article according to claim 1 , wherein the propylene homopolymer has 2,1 erythro regio-defects of equal to or below0.4 mol.-% determined by 13 C-NMR spectroscopy. 5. Injection molded article according to claim 1 , wherein the propylene homopolymer has a xylene cold soluble content (XCS) determined according ISO 16152 (25° C.) of below 4.0 wt.-%. 6. Injection molded article according to claim 1 , wherein the propylene homopolymer has a melting temperature of at least 158° C. 7. Injection molded article according to claim 1 , wherein the propylene homopolymer has a crystallization temperature of equal to or below 122° C. 8. Injection molded article according to claim 1 , wherein the propylene homopolymer is not visbroken. 9. Injection molded article according to claim 1 , wherein the propylene homopolymer has a flexural modulus measured at 23° C. according to ISO 178 of at least 1,350 MPa. 10. Injection molded article according to claim 1 , wherein the propylene homopolymer has a clarity measured according to ASTM D 1003/92 on injection molded specimen of 1 mm thickness of at least 55%. 11. Injection molded article according to claim 1 , wherein the injection molded article is a healthcare article. 12. Injection molded article according to claim 1 wherein the injection molded article is selected from the group consisting of syringes, pipette tips, and PCR equipment. 13. Injection molded article according to claim 1 , wherein the injection molded article has in its largest dimension a length of not more than 150 mm. 14. Injection molded article according to claim 1 , wherein the injection molded article has in its largest dimension a length of not more than 130 mm. 15. Injection molded article according to claim 1 , wherein the injection molded article comprises at least 75 wt.-%, based on the total weight of the injection molded article, of a propylene homopolymer having (a) a melt flow rate MFR 2 (230° C./2.16 kg) measured according to ISO 1133 in the range of 40 to 120 g/10min; (b) a pentad isotacticity (mmmm) of more than 92.5% determined by 13 C-NMR; and (c) a meso sequence length (MSL4) of 91.0 to 160; MSL4 is calculated by formula (1) MSL 4 = 2 * [ mmmm ] [ mmmr ] + 4 ( 1 ) wherein “[mmmm]” is % of mmmm pentads “[mmmr]” is % of mmmr pentads, determined by 13 C-NMR spectroscopy. 16. Process for producing an injection molded article of claim 1 , wherein the propylene homopolymer is injection molded, wherein further said propylene homopolymer has been obtained by polymerizing propylene in the presence of (a) a Ziegler-Natta catalyst (ZN-C) comprising compounds (TC) of a transition metal of Group 4 to 6 of IUPAC, a Group 2 metal compound (MC) and an internal donor (ID), wherein said internal donor (ID) is a non-phthalic compound; (b) a co-catalyst (Co), and (c) an external donor (ED). 17. Process according to claim 16 , wherein (a) the internal donor (ID) is selected from optionally substituted malonates, maleates, succinates, glutarates, cyclohexene-1,2-dicarboxylates, benzoates and derivatives and/or mixtures thereof; (b) the molar-ratio of co-catalyst (Co) to external donor (ED) [Co/ED] is 5 to 45.
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Manufacture of articles or shaped materials containing macromolecular substances (manufacture of semi-permeable membranes B01D67/00 - B01D71/00) · CPC title
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