Rui Li
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Rui Li has a total of 10 co-authors. Here are the top co-authors by number of shared publications:
- Jingjie Han
School of Chemical Engineering Qingdao University of Science and Technology Qingdao China
3 shared publications Xinru Zhang
School of Chemical Engineering, Qingdao University of Science and Technology Qingdao Shandong China
3 shared publicationsYanbing Hou
School of Chemical Engineering, Qingdao University of Science and Technology Qingdao Shandong China
3 shared publicationsAo Guo
Institute of Management and Humanities, Jingjiang College Jiangsu University Zhenjiang China
1 shared publicationRui Wang
School of Chemical Engineering Qingdao University of Science and Technology Qingdao China
1 shared publicationShixin Dong
School of Chemical Engineering, Qingdao University of Science and Technology Qingdao Shandong China
1 shared publication
Latest Publications
- 24 July 2026
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 143 (39) , e71252
Effect of Double Bridging of Epoxidized Natural Rubber on the Interface Compatibility of Starch Nanoparticles/Natural Rubber Latex Composites
To address the issues of significant polarity mismatch and weak interfacial bonding between polar starch nanoparticles (SNPs) and nonpolar natural rubber latex (NRL), epoxidized natural rubber (ENR) was introduced as an interfacial modifier in this work, aiming to optimize the interfacial interactions and comprehensive properties of SNPs/NRL composites. Mechanistic analysis revealed that ENR exerted a unique “bridging” effect: the epoxy groups on its molecular chains formed hydrogen‐bonded physical interactions with the hydroxyl groups on the surface of SNPs, while the carbon–carbon double bonds participated in the co‐vulcanization reaction of the NRL matrix, thereby constructing a dense interfacial cross‐linking network. This dual effect effectively inhibited the agglomeration of SNPs and significantly reduced the interfacial defects within the composites. The experimental results demonstrated that the optimal modification effect was achieved at an ENR loading of 5 phr. Compared with the neat control sample without ENR addition, the tensile strength of the composite was increased by 40.56%, the wet abrasion loss was reduced by 61.58%, the cross‐linking density reached the peak value, and the microscopic morphology of the composite exhibited a high degree of uniformity and densification. This work provides a theoretical basis for the interfacial design of high‐performance NRL‐based composites.
- 24 July 2026
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 143 (39) , e71252
Effect of Double Bridging of Epoxidized Natural Rubber on the Interface Compatibility of Starch Nanoparticles/Natural Rubber Latex Composites
To address the issues of significant polarity mismatch and weak interfacial bonding between polar starch nanoparticles (SNPs) and nonpolar natural rubber latex (NRL), epoxidized natural rubber (ENR) was introduced as an interfacial modifier in this work, aiming to optimize the interfacial interactions and comprehensive properties of SNPs/NRL composites. Mechanistic analysis revealed that ENR exerted a unique “bridging” effect: the epoxy groups on its molecular chains formed hydrogen‐bonded physical interactions with the hydroxyl groups on the surface of SNPs, while the carbon–carbon double bonds participated in the co‐vulcanization reaction of the NRL matrix, thereby constructing a dense interfacial cross‐linking network. This dual effect effectively inhibited the agglomeration of SNPs and significantly reduced the interfacial defects within the composites. The experimental results demonstrated that the optimal modification effect was achieved at an ENR loading of 5 phr. Compared with the neat control sample without ENR addition, the tensile strength of the composite was increased by 40.56%, the wet abrasion loss was reduced by 61.58%, the cross‐linking density reached the peak value, and the microscopic morphology of the composite exhibited a high degree of uniformity and densification. This work provides a theoretical basis for the interfacial design of high‐performance NRL‐based composites.
- 21 January 2025
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 142 (15)
A Type of Low‐Temperature Resistant Material Based on Ethylene Propylene Monomer/Polypropylene Thermoplastic Vulcanizates Compatibilized by Polyisobutylene
Thermoplastic vulcanized rubber (TPV) result in intermaterial incompatibility due to the thermodynamic incompatibility of the components that make up their soft and hard segments, which results in significant low‐temperature brittleness and poor mechanical properties of the material. And the low‐temperature properties of thermoplastic elastomers, especially based on ethylene propylene monomer/polypropylene (EPDM/PP) thermoplastic elastomers, and the corresponding mechanism of action have not been elucidated. The balance between low temperature performance and mechanical properties is a real challenge for TPV. In this paper, polyisobutylene (PIB1300) was introduced into the interstices of the molecular chain as an adhesive plasticizer to enhance the interfacial adhesion between PP and EPDM. The torque change showed that the presence of PIB1300 increased the interfacial interaction between PP and EPDM. The contact angle test and the calculation of the compatibilizer's position of action further confirmed that PIB1300 could be used as an effective compatibilizer to improve the compatibility of the material. When the amount of PIB1300 was 3 phr, EPDM/PP with both mechanical properties and compatibility, low temperature resistance, low temperature elasticity, and low temperature brittleness was finally determined, and the tensile strength of the material was 12.34 MPa, which was by 109.86%.
- 21 January 2025
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 142 (15)
A Type of Low‐Temperature Resistant Material Based on Ethylene Propylene Monomer/Polypropylene Thermoplastic Vulcanizates Compatibilized by Polyisobutylene
Thermoplastic vulcanized rubber (TPV) result in intermaterial incompatibility due to the thermodynamic incompatibility of the components that make up their soft and hard segments, which results in significant low‐temperature brittleness and poor mechanical properties of the material. And the low‐temperature properties of thermoplastic elastomers, especially based on ethylene propylene monomer/polypropylene (EPDM/PP) thermoplastic elastomers, and the corresponding mechanism of action have not been elucidated. The balance between low temperature performance and mechanical properties is a real challenge for TPV. In this paper, polyisobutylene (PIB1300) was introduced into the interstices of the molecular chain as an adhesive plasticizer to enhance the interfacial adhesion between PP and EPDM. The torque change showed that the presence of PIB1300 increased the interfacial interaction between PP and EPDM. The contact angle test and the calculation of the compatibilizer's position of action further confirmed that PIB1300 could be used as an effective compatibilizer to improve the compatibility of the material. When the amount of PIB1300 was 3 phr, EPDM/PP with both mechanical properties and compatibility, low temperature resistance, low temperature elasticity, and low temperature brittleness was finally determined, and the tensile strength of the material was 12.34 MPa, which was by 109.86%.
- 19 January 2025
- Published by Wiley in Polymer Engineering & Science
- Vol. 65 (3) , 1327-1339
Effect of ligand bond structure on self‐healing properties of XNBR / CuCl 2 at different temperatures
Metal coordination bonds can be coordinated to specific functional groups in polymers. This special coordination can give the material excellent self‐healing and mechanical properties. Nitrile rubber (XNBR)/CuCl 2 composites were prepared by solid‐state blending. By changing the coordination reaction temperature, different coordination bonds were formed between the nitrile rubber and copper ions. The starting temperature of the coordination reaction was determined to be 100°C by observing the changes in the coordination reaction curve. With the increase of temperature from 100°C to 190°C, the copper ions' oxidation state was raised to 3, while part of C ≡ N was transformed to C=N at high temperature. Quantitative analysis revealed that the linear coordination [Cu 2+ –N L ] was predominantly triple‐coordinated, and the curved coordination [Cu 3+ –N B ] was coordinated in the form of ionic clusters. In addition to this, the formation of linear coordination bonds was easier and more reversible based on the calculation of the apparent activation energy of the coordination reaction. Macroscopically, the mechanical properties and self‐repairing ability of XNBR/CuCl 2 ‐10‐100°C were higher than those of XNBR/CuCl 2 ‐10‐190°C. The design of cross‐linked XNBR with good mechanical properties and recycling performance was of great significance in protecting the environment and realizing sustainable development. Highlights: XNBR/CuCl 2 ‐10‐100°C composites mainly form linear coordination [Cu 2+ –3N L ]. XNBR/CuCl 2 ‐10‐190°C composites form bending coordination [Cu 3+ –NB]. [Cu 3+ –N B ] is stronger than [Cu 2+ –N L ] but less reversible.
- 19 January 2025
- Published by Wiley in Polymer Engineering & Science
- Vol. 65 (3) , 1327-1339
Effect of ligand bond structure on self‐healing properties of XNBR / CuCl 2 at different temperatures
Metal coordination bonds can be coordinated to specific functional groups in polymers. This special coordination can give the material excellent self‐healing and mechanical properties. Nitrile rubber (XNBR)/CuCl 2 composites were prepared by solid‐state blending. By changing the coordination reaction temperature, different coordination bonds were formed between the nitrile rubber and copper ions. The starting temperature of the coordination reaction was determined to be 100°C by observing the changes in the coordination reaction curve. With the increase of temperature from 100°C to 190°C, the copper ions' oxidation state was raised to 3, while part of C ≡ N was transformed to C=N at high temperature. Quantitative analysis revealed that the linear coordination [Cu 2+ –N L ] was predominantly triple‐coordinated, and the curved coordination [Cu 3+ –N B ] was coordinated in the form of ionic clusters. In addition to this, the formation of linear coordination bonds was easier and more reversible based on the calculation of the apparent activation energy of the coordination reaction. Macroscopically, the mechanical properties and self‐repairing ability of XNBR/CuCl 2 ‐10‐100°C were higher than those of XNBR/CuCl 2 ‐10‐190°C. The design of cross‐linked XNBR with good mechanical properties and recycling performance was of great significance in protecting the environment and realizing sustainable development. Highlights: XNBR/CuCl 2 ‐10‐100°C composites mainly form linear coordination [Cu 2+ –3N L ]. XNBR/CuCl 2 ‐10‐190°C composites form bending coordination [Cu 3+ –NB]. [Cu 3+ –N B ] is stronger than [Cu 2+ –N L ] but less reversible.