Lingbin Lu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Lingbin Lu has a total of 80 co-authors. Here are the top co-authors by number of shared publications:
Yang Cao
State Key Laboratory of Marine Resource Utilization in South China Sea, College of Materials and Chemical Engineering, Hainan University, Haikou, Hainan, China
10 shared publicationsChenxi Niu
Special Glass Key Lab of Hainan Province (Hainan University), School of Materials Science and Engineering, Hainan University, Haikou 570228, China
6 shared publicationsQian Fu
Special Glass Key Lab of Hainan Province (Hainan University), School of Materials Science and Engineering, Hainan University, Haikou 570228, China
6 shared publicationsYouhui Chen
Special Glass Key Lab of Hainan Province (Hainan University), School of Materials Science and Engineering, Hainan University, Haikou 570228, China
6 shared publicationsAng Li
Key Laboratory of Advanced Materials of Tropical Island Resources (Hainan University)
5 shared publicationsLin Shao
Key Laboratory of Advanced Materials of Tropical Island Resources (Hainan University), Ministry of Education, Haikou, 570228, China; State Key Laboratory of Marine Resource Utilization in South China Sea (Hainan University), Haikou, 570228, China; Special Glass Key Lab of Hainan Province, Haikou, 570228, China; College of Materials and Chemical Engineering, Hainan University, Haikou, 570228, China
5 shared publications
Latest Publications
- Open Access
Molecularly Engineered Aza-Crown Ether Functionalized Sodium Alginate Aerogels for Highly Selective and Sustainable Cu2+ Removal
Developing sustainable and molecularly selective adsorbents for heavy-metal removal remains a critical challenge in water purification. Herein, we report a green molecular-engineering approach for fabricating aza-crown ether functionalized sodium alginate aerogels (ACSA) capable of highly selective Cu2+ capture. The aerogels were synthesized via saccharide-ring oxidation, Cu2+-templated self-assembly, and reductive amination, enabling the covalent integration of aza-crown ether motifs within a hierarchically porous biopolymer matrix. Structural analyses (FTIR, 13C NMR, XPS, SEM, TGA) confirmed the in situ formation of macrocyclic N/O coordination sites. Owing to their interconnected porosity and chemically stable framework, ACSA exhibited rapid sorption kinetics following a pseudo-second-order model (R2 = 0.999) and a Langmuir maximum adsorption capacity of 150.82 mg·g−1. The material displayed remarkable Cu2+ selectivity over Zn2+, Cd2+, and Ni2+, arising from the precise alignment between Cu2+ ionic radius (0.73 Å) and crown-cavity dimensions, synergistic N/O chelation, and Jahn-Teller stabilization. Over four regeneration cycles, ACSA retained more than 80% of its original adsorption capacity, confirming excellent durability and reusability. This saccharide-ring modification strategy eliminates crown-ether leaching and weak anchoring, offering a scalable and environmentally benign route to bio-based adsorbents that combine molecular recognition with structural stability for efficient Cu2+ remediation and beyond.
Open AccessMolecularly Engineered Aza-Crown Ether Functionalized Sodium Alginate Aerogels for Highly Selective and Sustainable Cu2+ Removal
Developing sustainable and molecularly selective adsorbents for heavy-metal removal remains a critical challenge in water purification. Herein, we report a green molecular-engineering approach for fabricating aza-crown ether functionalized sodium alginate aerogels (ACSA) capable of highly selective Cu2+ capture. The aerogels were synthesized via saccharide-ring oxidation, Cu2+-templated self-assembly, and reductive amination, enabling the covalent integration of aza-crown ether motifs within a hierarchically porous biopolymer matrix. Structural analyses (FTIR, 13C NMR, XPS, SEM, TGA) confirmed the in situ formation of macrocyclic N/O coordination sites. Owing to their interconnected porosity and chemically stable framework, ACSA exhibited rapid sorption kinetics following a pseudo-second-order model (R2 = 0.999) and a Langmuir maximum adsorption capacity of 150.82 mg·g−1. The material displayed remarkable Cu2+ selectivity over Zn2+, Cd2+, and Ni2+, arising from the precise alignment between Cu2+ ionic radius (0.73 Å) and crown-cavity dimensions, synergistic N/O chelation, and Jahn-Teller stabilization. Over four regeneration cycles, ACSA retained more than 80% of its original adsorption capacity, confirming excellent durability and reusability. This saccharide-ring modification strategy eliminates crown-ether leaching and weak anchoring, offering a scalable and environmentally benign route to bio-based adsorbents that combine molecular recognition with structural stability for efficient Cu2+ remediation and beyond.
- 3 June 2025
- Published by Elsevier in International Journal of Biological Macromolecules
- Vol. 317 (Pt 2) , 144942
A synergistic flexibility management strategy for self-healing carboxymethyl cellulose hydrogel with strain responsiveness based on p-phenylenediamine
- 3 June 2025
- Published by Elsevier in International Journal of Biological Macromolecules
- Vol. 317 (Pt 2) , 144942
A synergistic flexibility management strategy for self-healing carboxymethyl cellulose hydrogel with strain responsiveness based on p-phenylenediamine
- 16 April 2025
- Published by Elsevier in International Journal of Biological Macromolecules
- Vol. 310 (Pt 1) , 143257
Eco-friendly alginate-urea-fluroxypyr hydrogel for sustainable agriculture: A comprehensive approach to integrated fertilizer delivery and weed control
- 16 April 2025
- Published by Elsevier in International Journal of Biological Macromolecules
- Vol. 310 (Pt 1) , 143257
Eco-friendly alginate-urea-fluroxypyr hydrogel for sustainable agriculture: A comprehensive approach to integrated fertilizer delivery and weed control
- 21 September 2024
- Published by Elsevier in International Journal of Biological Macromolecules
- Vol. 280 (Pt 2) , 135883
Liquid crystal phase behavior of oxalated cellulose nanocrystal and optical films with controllable structural color induced by centripetal force
- 21 September 2024
- Published by Elsevier in International Journal of Biological Macromolecules
- Vol. 280 (Pt 2) , 135883
Liquid crystal phase behavior of oxalated cellulose nanocrystal and optical films with controllable structural color induced by centripetal force
- 30 January 2024
- Published by Elsevier in International Journal of Biological Macromolecules
- Vol. 261, 129865
Construction of strain responsive Ti-containing carboxymethyl cellulose hydrogel with transitional coordination precursor
- 30 January 2024
- Published by Elsevier in International Journal of Biological Macromolecules
- Vol. 261, 129865
Construction of strain responsive Ti-containing carboxymethyl cellulose hydrogel with transitional coordination precursor
- 12 December 2023
- Published by Elsevier in Carbohydrate Polymers
- Vol. 327, 121676
An eco-friendly versatile superabsorbent hydrogel based on sodium alginate and urea for soil improvement with a synchronous chemical loading strategy
- 12 December 2023
- Published by Elsevier in Carbohydrate Polymers
- Vol. 327, 121676
An eco-friendly versatile superabsorbent hydrogel based on sodium alginate and urea for soil improvement with a synchronous chemical loading strategy
- 23 February 2023
- Published by American Chemical Society (ACS) in Chemistry of Materials
- Vol. 35 (5) , 1991-2005
Dual-Mechanism-Driven Environmental-Friendly Fast Self-Healing Ionic Hydrogels with Excellent Sensitivity to Strain Responsiveness
- 23 February 2023
- Published by American Chemical Society (ACS) in Chemistry of Materials
- Vol. 35 (5) , 1991-2005
Dual-Mechanism-Driven Environmental-Friendly Fast Self-Healing Ionic Hydrogels with Excellent Sensitivity to Strain Responsiveness
- Open Access
Advances in Asymmetric Wettable Janus Materials for Oil–Water Separation
The frequent occurrence of crude oil spills and the indiscriminate discharge of oily wastewater have caused serious environmental pollution. The existing separation methods have some defects and are not suitable for complex oil–water emulsions. Therefore, the efficient separation of complex oil–water emulsions has been of great interest to researchers. Asymmetric wettable Janus materials, which can efficiently separate complex oil–water emulsions, have attracted widespread attention. This comprehensive review systematically summarizes the research progress of asymmetric wettable Janus materials for oil–water separation in the last decade, and introduces, in detail, the preparation methods of them. Specifically, the latest research results of two-dimensional Janus materials, three-dimensional Janus materials, smart responsive Janus materials, and environmentally friendly Janus materials for oil–water separation are elaborated. Finally, ongoing challenges and outlook for the future research of asymmetric wettable Janus materials are presented.
Open AccessAdvances in Asymmetric Wettable Janus Materials for Oil–Water Separation
The frequent occurrence of crude oil spills and the indiscriminate discharge of oily wastewater have caused serious environmental pollution. The existing separation methods have some defects and are not suitable for complex oil–water emulsions. Therefore, the efficient separation of complex oil–water emulsions has been of great interest to researchers. Asymmetric wettable Janus materials, which can efficiently separate complex oil–water emulsions, have attracted widespread attention. This comprehensive review systematically summarizes the research progress of asymmetric wettable Janus materials for oil–water separation in the last decade, and introduces, in detail, the preparation methods of them. Specifically, the latest research results of two-dimensional Janus materials, three-dimensional Janus materials, smart responsive Janus materials, and environmentally friendly Janus materials for oil–water separation are elaborated. Finally, ongoing challenges and outlook for the future research of asymmetric wettable Janus materials are presented.