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Crystallization, mechanical, and heat resistance performances of copolymer polypropylene modified by α nucleating agent
Polypropylene (PP) was a very practical and important thermoplastic, which was widely used in various fields due to its low cost, universal, and corrosion resistance. However, the moderate mechanical and heat resistance properties of PP limited its application in some special fields. In this paper,...
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Published in: | Polymer engineering and science 2024-11, Vol.64 (11), p.5539-5550 |
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creator | Ding, Shubing Jin, Congcong Li, Zhuo Dun, Dongxing Xue, Yu Leng, Shengmin Zhang, Yan'e Zhou, Hongfu |
description | Polypropylene (PP) was a very practical and important thermoplastic, which was widely used in various fields due to its low cost, universal, and corrosion resistance. However, the moderate mechanical and heat resistance properties of PP limited its application in some special fields. In this paper, nucleating agents NP‐657 were added to further improve its mechanical and heat resistance performances of PP (300H). Furthermore, the heterogeneous nucleation of NP‐657 reduced the crystal size and increased the crystal density of 300H. With the rise of NP‐657 content, the crystallization rate of different PP systems increased significantly, such as the t1/2 of 300H‐0.2 reduced by 31.9 min in comparison with that of 300H at 140°C. At the same time, the crystallinity of 300H‐0.05 with 0.05 wt.% NP‐657 increased by about 5.96% compared with 300H. In addition, 300H‐0.05 has the highest tensile strength (23.9 ± 0.6 MPa), flexural modulus (1273.3 ± 67.3 MPa), and the highest thermal deformation temperature (88.5 ± 7.7°C) in different PP systems. In general, this paper provided a reference for the fabrication of PP with satisfactory mechanical and heat resistance performances.
Highlights
300H‐0.05 had a maximum crystallinity of 40.8 ± 0.2% in different PP systems.
The flexural modulus of 300H‐0.05 was 434 MPa higher than that of 300H.
The tensile strength of 300H‐0.05 increased to 23.9 ± 0.6 MPa.
300H had the highest thermal deformation temperature of 88.5 ± 7.7°C.
Modification mechanism of α nucleating agent oncrystallization behaviors of PP. |
doi_str_mv | 10.1002/pen.26932 |
format | article |
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Highlights
300H‐0.05 had a maximum crystallinity of 40.8 ± 0.2% in different PP systems.
The flexural modulus of 300H‐0.05 was 434 MPa higher than that of 300H.
The tensile strength of 300H‐0.05 increased to 23.9 ± 0.6 MPa.
300H had the highest thermal deformation temperature of 88.5 ± 7.7°C.
Modification mechanism of α nucleating agent oncrystallization behaviors of PP.</description><identifier>ISSN: 0032-3888</identifier><identifier>EISSN: 1548-2634</identifier><identifier>DOI: 10.1002/pen.26932</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Copolymers ; Corrosion resistance ; Crystallinity ; Crystallization ; flexural modulus ; Heat resistance ; Modulus of rupture in bending ; nucleating agent ; Nucleation ; Polypropylene ; Tensile strength ; thermal deformation temperature ; Thermal resistance</subject><ispartof>Polymer engineering and science, 2024-11, Vol.64 (11), p.5539-5550</ispartof><rights>2024 Society of Plastics Engineers.</rights><rights>2024 Society of Plastics Engineers</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1872-ab7e593092f071bfd4e5b1e6f0b69abe0c579a6d82a0697aafa0562fd1fad0a33</cites><orcidid>0000-0002-9154-1798</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Ding, Shubing</creatorcontrib><creatorcontrib>Jin, Congcong</creatorcontrib><creatorcontrib>Li, Zhuo</creatorcontrib><creatorcontrib>Dun, Dongxing</creatorcontrib><creatorcontrib>Xue, Yu</creatorcontrib><creatorcontrib>Leng, Shengmin</creatorcontrib><creatorcontrib>Zhang, Yan'e</creatorcontrib><creatorcontrib>Zhou, Hongfu</creatorcontrib><title>Crystallization, mechanical, and heat resistance performances of copolymer polypropylene modified by α nucleating agent</title><title>Polymer engineering and science</title><description>Polypropylene (PP) was a very practical and important thermoplastic, which was widely used in various fields due to its low cost, universal, and corrosion resistance. However, the moderate mechanical and heat resistance properties of PP limited its application in some special fields. In this paper, nucleating agents NP‐657 were added to further improve its mechanical and heat resistance performances of PP (300H). Furthermore, the heterogeneous nucleation of NP‐657 reduced the crystal size and increased the crystal density of 300H. With the rise of NP‐657 content, the crystallization rate of different PP systems increased significantly, such as the t1/2 of 300H‐0.2 reduced by 31.9 min in comparison with that of 300H at 140°C. At the same time, the crystallinity of 300H‐0.05 with 0.05 wt.% NP‐657 increased by about 5.96% compared with 300H. In addition, 300H‐0.05 has the highest tensile strength (23.9 ± 0.6 MPa), flexural modulus (1273.3 ± 67.3 MPa), and the highest thermal deformation temperature (88.5 ± 7.7°C) in different PP systems. In general, this paper provided a reference for the fabrication of PP with satisfactory mechanical and heat resistance performances.
Highlights
300H‐0.05 had a maximum crystallinity of 40.8 ± 0.2% in different PP systems.
The flexural modulus of 300H‐0.05 was 434 MPa higher than that of 300H.
The tensile strength of 300H‐0.05 increased to 23.9 ± 0.6 MPa.
300H had the highest thermal deformation temperature of 88.5 ± 7.7°C.
Modification mechanism of α nucleating agent oncrystallization behaviors of PP.</description><subject>Copolymers</subject><subject>Corrosion resistance</subject><subject>Crystallinity</subject><subject>Crystallization</subject><subject>flexural modulus</subject><subject>Heat resistance</subject><subject>Modulus of rupture in bending</subject><subject>nucleating agent</subject><subject>Nucleation</subject><subject>Polypropylene</subject><subject>Tensile strength</subject><subject>thermal deformation temperature</subject><subject>Thermal resistance</subject><issn>0032-3888</issn><issn>1548-2634</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp1kMtOwzAQRS0EEqWw4A8ssUJqWj_yXKKqPKQKWMA6miTj1lViBzsVhL_iR_gmUsKW1Z3FmTujQ8glZ3POmFi0aOYizqQ4IhMehWkgYhkekwljUgQyTdNTcub9jg2sjLIJ-Vi63ndQ1_oTOm3NjDZYbsHoEuoZBVPRLUJHHXo9YKZE2qJT1jWH2VOraGlbW_cNOnrI1tm2r9EgbWyllcaKFj39_qJmX9ZDkzYbChs03Tk5UVB7vPjLKXm9Xb0s74P1093D8mYdlDxNRABFglEmWSYUS3ihqhCjgmOsWBFnUCAroySDuEoFsDhLABSwKBaq4goqBlJOydXYO3z2tkff5Tu7d2Y4mUsuIslCPuiakuuRKp313qHKW6cbcH3OWX4Qmw9i81-xA7sY2XddY_8_mD-vHseNHxizfek</recordid><startdate>202411</startdate><enddate>202411</enddate><creator>Ding, Shubing</creator><creator>Jin, Congcong</creator><creator>Li, Zhuo</creator><creator>Dun, Dongxing</creator><creator>Xue, Yu</creator><creator>Leng, Shengmin</creator><creator>Zhang, Yan'e</creator><creator>Zhou, Hongfu</creator><general>John Wiley & Sons, Inc</general><general>Blackwell Publishing Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope><orcidid>https://orcid.org/0000-0002-9154-1798</orcidid></search><sort><creationdate>202411</creationdate><title>Crystallization, mechanical, and heat resistance performances of copolymer polypropylene modified by α nucleating agent</title><author>Ding, Shubing ; Jin, Congcong ; Li, Zhuo ; Dun, Dongxing ; Xue, Yu ; Leng, Shengmin ; Zhang, Yan'e ; Zhou, Hongfu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1872-ab7e593092f071bfd4e5b1e6f0b69abe0c579a6d82a0697aafa0562fd1fad0a33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Copolymers</topic><topic>Corrosion resistance</topic><topic>Crystallinity</topic><topic>Crystallization</topic><topic>flexural modulus</topic><topic>Heat resistance</topic><topic>Modulus of rupture in bending</topic><topic>nucleating agent</topic><topic>Nucleation</topic><topic>Polypropylene</topic><topic>Tensile strength</topic><topic>thermal deformation temperature</topic><topic>Thermal resistance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ding, Shubing</creatorcontrib><creatorcontrib>Jin, Congcong</creatorcontrib><creatorcontrib>Li, Zhuo</creatorcontrib><creatorcontrib>Dun, Dongxing</creatorcontrib><creatorcontrib>Xue, Yu</creatorcontrib><creatorcontrib>Leng, Shengmin</creatorcontrib><creatorcontrib>Zhang, Yan'e</creatorcontrib><creatorcontrib>Zhou, Hongfu</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Polymer engineering and science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ding, Shubing</au><au>Jin, Congcong</au><au>Li, Zhuo</au><au>Dun, Dongxing</au><au>Xue, Yu</au><au>Leng, Shengmin</au><au>Zhang, Yan'e</au><au>Zhou, Hongfu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Crystallization, mechanical, and heat resistance performances of copolymer polypropylene modified by α nucleating agent</atitle><jtitle>Polymer engineering and science</jtitle><date>2024-11</date><risdate>2024</risdate><volume>64</volume><issue>11</issue><spage>5539</spage><epage>5550</epage><pages>5539-5550</pages><issn>0032-3888</issn><eissn>1548-2634</eissn><abstract>Polypropylene (PP) was a very practical and important thermoplastic, which was widely used in various fields due to its low cost, universal, and corrosion resistance. However, the moderate mechanical and heat resistance properties of PP limited its application in some special fields. In this paper, nucleating agents NP‐657 were added to further improve its mechanical and heat resistance performances of PP (300H). Furthermore, the heterogeneous nucleation of NP‐657 reduced the crystal size and increased the crystal density of 300H. With the rise of NP‐657 content, the crystallization rate of different PP systems increased significantly, such as the t1/2 of 300H‐0.2 reduced by 31.9 min in comparison with that of 300H at 140°C. At the same time, the crystallinity of 300H‐0.05 with 0.05 wt.% NP‐657 increased by about 5.96% compared with 300H. In addition, 300H‐0.05 has the highest tensile strength (23.9 ± 0.6 MPa), flexural modulus (1273.3 ± 67.3 MPa), and the highest thermal deformation temperature (88.5 ± 7.7°C) in different PP systems. In general, this paper provided a reference for the fabrication of PP with satisfactory mechanical and heat resistance performances.
Highlights
300H‐0.05 had a maximum crystallinity of 40.8 ± 0.2% in different PP systems.
The flexural modulus of 300H‐0.05 was 434 MPa higher than that of 300H.
The tensile strength of 300H‐0.05 increased to 23.9 ± 0.6 MPa.
300H had the highest thermal deformation temperature of 88.5 ± 7.7°C.
Modification mechanism of α nucleating agent oncrystallization behaviors of PP.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><doi>10.1002/pen.26932</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-9154-1798</orcidid></addata></record> |
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subjects | Copolymers Corrosion resistance Crystallinity Crystallization flexural modulus Heat resistance Modulus of rupture in bending nucleating agent Nucleation Polypropylene Tensile strength thermal deformation temperature Thermal resistance |
title | Crystallization, mechanical, and heat resistance performances of copolymer polypropylene modified by α nucleating agent |
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