Linjia Huang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Linjia Huang has a total of 22 co-authors. Here are the top co-authors by number of shared publications:
Huanling Li
Guangdong Acad Sci, Inst Chem Engn, Guangdong Prov Key Lab Ind Surfactant, Guangzhou 510665, Peoples R China
2 shared publications- Kangle Jia
Institute of Chemical Engineering
2 shared publications Xiaoshan Zheng
Guangdong Acad Sci, Inst Chem Engn, Guangdong Prov Key Lab Ind Surfactant, Guangzhou 510665, Peoples R China
2 shared publications- Anbo Luan
Guangdong Research Institute of Petrochemical and Fine Chemical Engineering, Guangzhou 510665, China
1 shared publication Jinlan Xin
Guangdong Acad Sci, Inst Chem Engn, Guangdong Prov Key Lab Ind Surfactant, Guangzhou 510665, Peoples R China
1 shared publicationJunjie Zhang
Guangdong Provincial Key Laboratory of Industrial Surfactant, Institute of Chemical Engineering Guangdong Academy of Sciences Guangzhou Guangdong 510000 P. R. China
1 shared publication
Latest Publications
- 1 January 2022
- Published by Shanghai Institute of Organic Chemistry in Acta Chimica Sinica
- Vol. 80 (6) , 765-771
pH-Responsive Pickering Emulsions Synergistically Stabilized by Maleopimaric Acid and Alumina Nanoparticles
- 1 January 2022
- Published by Shanghai Institute of Organic Chemistry in Acta Chimica Sinica
- Vol. 80 (6) , 765-771
pH-Responsive Pickering Emulsions Synergistically Stabilized by Maleopimaric Acid and Alumina Nanoparticles
- 17 April 2021
- Published by Wiley in Macromolecular Rapid Communications
- Vol. 42 (11) , 2100085
Electroinduced Reconfiguration of Complex Emulsions for Fabrication of Polymer Particles with Tunable Morphology
Continuous morphological control of anisotropic particles is always an important challenge in the field of materials. In this study, a new strategy for continuous fabrication of polymer particles with various morphologies induced by electricity is reported using complex emulsions as template. A synthetic electro‐responsive surfactant containing ferrocene group is used to prepare complex emulsions, which contain a polymerizable monomer as inner phase. With the increasing time of electrical stimulation on the complex emulsions, hollow, hemispherical, mushroom‐like, and spherical particles are constructed successively after photopolymerization. The Marangoni effect caused by the heterogeneity in the interfacial tension at the droplet surface is the reason for the reconfigurable morphology of the complex emulsion. The controllable complex emulsions by electricity present a versatile platform for constructing fine control of the microstructure and shape anisotropy of particles having customized shapes and functionalities, opening a new possibility for designing sophisticated architectures.
- 17 April 2021
- Published by Wiley in Macromolecular Rapid Communications
- Vol. 42 (11) , 2100085
Electroinduced Reconfiguration of Complex Emulsions for Fabrication of Polymer Particles with Tunable Morphology
Continuous morphological control of anisotropic particles is always an important challenge in the field of materials. In this study, a new strategy for continuous fabrication of polymer particles with various morphologies induced by electricity is reported using complex emulsions as template. A synthetic electro‐responsive surfactant containing ferrocene group is used to prepare complex emulsions, which contain a polymerizable monomer as inner phase. With the increasing time of electrical stimulation on the complex emulsions, hollow, hemispherical, mushroom‐like, and spherical particles are constructed successively after photopolymerization. The Marangoni effect caused by the heterogeneity in the interfacial tension at the droplet surface is the reason for the reconfigurable morphology of the complex emulsion. The controllable complex emulsions by electricity present a versatile platform for constructing fine control of the microstructure and shape anisotropy of particles having customized shapes and functionalities, opening a new possibility for designing sophisticated architectures.
- Open Access
Polypropylene Glycol-Polyoxytetramethylene Glycol Multiblock Copolymers with High Molecular Weight: Synthesis, Characterization, and Silanization
The high crystallization at room temperature and high cost of polyoxytetramethylene glycol (PTMG) have become obstacles to its application. To overcome these problems, a segment of PTMG can be incorporated into a block copolymer. In this work, polypropylene (PPO) glycol-polyoxytetramethylene (PPO-PTMG) multiblock copolymers were designed and synthesized through a chain extension between hydroxyl (OH)-terminated PPO and PTMG oligomers. The chain extenders, feed ratios of the catalyst/chain extender/OH groups, reaction temperature, and time were optimized several times to obtain a PPO-PTMG with low crystallization and high molecular weight. Multiblock copolymers with low crystallization and high average molecular weight (Mn = 1.0–1.4 × 104 Dalton) were harvested using m-phthaloyl chloride as the chain extender. The OH-terminated PPO-PTMG multiblock copolymer with high Mn and a functionality near two was further siliconized by 3-isocyanatopropyltrimethoxysilane to synthesize a novel silyl-terminated polyether. This polyether has an appropriate vulcanizing property and potential applications in sealants/adhesive fields.
Open AccessPolypropylene Glycol-Polyoxytetramethylene Glycol Multiblock Copolymers with High Molecular Weight: Synthesis, Characterization, and Silanization
The high crystallization at room temperature and high cost of polyoxytetramethylene glycol (PTMG) have become obstacles to its application. To overcome these problems, a segment of PTMG can be incorporated into a block copolymer. In this work, polypropylene (PPO) glycol-polyoxytetramethylene (PPO-PTMG) multiblock copolymers were designed and synthesized through a chain extension between hydroxyl (OH)-terminated PPO and PTMG oligomers. The chain extenders, feed ratios of the catalyst/chain extender/OH groups, reaction temperature, and time were optimized several times to obtain a PPO-PTMG with low crystallization and high molecular weight. Multiblock copolymers with low crystallization and high average molecular weight (Mn = 1.0–1.4 × 104 Dalton) were harvested using m-phthaloyl chloride as the chain extender. The OH-terminated PPO-PTMG multiblock copolymer with high Mn and a functionality near two was further siliconized by 3-isocyanatopropyltrimethoxysilane to synthesize a novel silyl-terminated polyether. This polyether has an appropriate vulcanizing property and potential applications in sealants/adhesive fields.