Zhenmin Liu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Zhenmin Liu has a total of 34 co-authors. Here are the top co-authors by number of shared publications:
- Baosheng Liu
Taiyuan University of Science and Technology
2 shared publications Bin Li
School of Chemical and Biological Engineering, Taiyuan University of Science and Technology, Taiyuan 030024, China
1 shared publication- Chuangji Gao
College of Chemistry and Biological Engineering, Taiyuan University of Science and Technology, Taiyuan 030024, China
1 shared publication - Erzhuang Zhang
College of Chemistry and Biological Engineering, Taiyuan University of Science and Technology, Taiyuan 030024, China
1 shared publication Fengrui Qiao
School of Chemical and Biological Engineering, Taiyuan University of Science and Technology, Taiyuan 030024, China
1 shared publicationHai-Qiang Lu
College of Chemical Engineering and Technology, Taiyuan University of Science and Technology, Taiyuan 030024, China
1 shared publication
Latest Publications
- 22 June 2026
- Published by Springer Nature in Journal of the Iranian Chemical Society
- Vol. 23 (7)
Calcination-induced structural modulation of Li/Mg catalysts for efficient glycerol carbonate synthesis
- 22 June 2026
- Published by Springer Nature in Journal of the Iranian Chemical Society
- Vol. 23 (7)
Calcination-induced structural modulation of Li/Mg catalysts for efficient glycerol carbonate synthesis
- 8 December 2023
- Published by American Chemical Society (ACS) in ACS Applied Nano Materials
- Vol. 6 (24) , 22865-22875
Nanoporous Metal–Organic Framework Adsorbent Constructed via Ligand Tailoring for Rare-Earth Metal Ion Recovery
- 8 December 2023
- Published by American Chemical Society (ACS) in ACS Applied Nano Materials
- Vol. 6 (24) , 22865-22875
Nanoporous Metal–Organic Framework Adsorbent Constructed via Ligand Tailoring for Rare-Earth Metal Ion Recovery
- Open Access
- 26 July 2023
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 13 (33) , 22815-22823
Mesoporous sol–gel silica supported vanadium oxide as effective catalysts in oxidative dehydrogenation of propane to propylene
Strongly-interacted [OV(OSi) 3 ] sites with mesoporous silica, triggered by a surfactant-modified sol–gel method, promotes the selective oxidative dehydrogenation of propane to propylene.
- 26 July 2023
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 13 (33) , 22815-22823
Open AccessMesoporous sol–gel silica supported vanadium oxide as effective catalysts in oxidative dehydrogenation of propane to propylene
Strongly-interacted [OV(OSi) 3 ] sites with mesoporous silica, triggered by a surfactant-modified sol–gel method, promotes the selective oxidative dehydrogenation of propane to propylene.
- 19 May 2023
- Published by Elsevier in Separation and Purification Technology
- Vol. 320, 124062
Introducing dense sulfonic acid in metal–organic framework for effective adsorption of radioactive barium ion
- 19 May 2023
- Published by Elsevier in Separation and Purification Technology
- Vol. 320, 124062
Introducing dense sulfonic acid in metal–organic framework for effective adsorption of radioactive barium ion
- Open Access
Synthesis and Performance of Double-Chain Quaternary Ammonium Salt Glucosamide Surfactants
A series of double-chain quaternary ammonium salt surfactants N-[N′[3-(gluconamide)] propyl-N′-alkyl]propyl-N,N-dimethyl-N-alkyl ammonium bromide (CnDDGPB, where n represents a hydrocarbon chain length of 8, 10, 12, 14 and 16) were successfully synthesized from D (+)-glucose δ-lactone, N,N-dimethyldipropylenetriamine, and bromoalkane using a two-step method consisting of a proamine-ester reaction and postquaternization. Their surface activity, adsorption, and aggregation behavior in aqueous solution were investigated via measurements of dynamic/static surface tension, contact angle, dynamic light scattering, and transmission electron microscopy. An analysis of their application performance in terms of wettability, emulsifying properties, toxicity, and antibacterial properties was conducted. The results show that with increasing the carbon chain length of the CnDDGPB surfactants, their critical micelle concentration (CMC) increased and the pC20 and efficiency in the interface adsorption of the target product gradually decreased. Moreover, the influence of the hydrophobic carbon chain length on the surface of polytetrafluoroethylene (PTFE) was even greater for the wetting effect, reducing the contact angle to 32° within the length range of C8–C14. The results of the contact angle change and the wettability experiments proved that C10DDGPB exhibited the best wettability. The liquid paraffin and soybean oil emulsification ability of CnDDGPB showed an upward trend followed by a downward trend with the growth of the carbon chain, with C12DDGPB exhibiting the best emulsification performance. The Dlong/Dshort ratio was far lower than 1, which indicates mixed-kinetic adsorption. The surfactants formed spherical micelles and showed a unique aggregation behavior in aqueous solution, which showed an increase–decrease–increase trend with the change in concentration. A cell toxicity and acute oral toxicity experiment showed that the CnDDGPB surfactants were less toxic than the commonly used surfactant dodecyldimethylbenzyl ammonium chloride (1227). In addition, at a concentration of 150 ppm, CnDDGPB exhibited the same bacteriostatic effect as 1227 at a concentration of 100 ppm. The results demonstrate that sugar-based amide cationic surfactants are promising as environmentally friendly disinfection products.
Open AccessSynthesis and Performance of Double-Chain Quaternary Ammonium Salt Glucosamide Surfactants
A series of double-chain quaternary ammonium salt surfactants N-[N′[3-(gluconamide)] propyl-N′-alkyl]propyl-N,N-dimethyl-N-alkyl ammonium bromide (CnDDGPB, where n represents a hydrocarbon chain length of 8, 10, 12, 14 and 16) were successfully synthesized from D (+)-glucose δ-lactone, N,N-dimethyldipropylenetriamine, and bromoalkane using a two-step method consisting of a proamine-ester reaction and postquaternization. Their surface activity, adsorption, and aggregation behavior in aqueous solution were investigated via measurements of dynamic/static surface tension, contact angle, dynamic light scattering, and transmission electron microscopy. An analysis of their application performance in terms of wettability, emulsifying properties, toxicity, and antibacterial properties was conducted. The results show that with increasing the carbon chain length of the CnDDGPB surfactants, their critical micelle concentration (CMC) increased and the pC20 and efficiency in the interface adsorption of the target product gradually decreased. Moreover, the influence of the hydrophobic carbon chain length on the surface of polytetrafluoroethylene (PTFE) was even greater for the wetting effect, reducing the contact angle to 32° within the length range of C8–C14. The results of the contact angle change and the wettability experiments proved that C10DDGPB exhibited the best wettability. The liquid paraffin and soybean oil emulsification ability of CnDDGPB showed an upward trend followed by a downward trend with the growth of the carbon chain, with C12DDGPB exhibiting the best emulsification performance. The Dlong/Dshort ratio was far lower than 1, which indicates mixed-kinetic adsorption. The surfactants formed spherical micelles and showed a unique aggregation behavior in aqueous solution, which showed an increase–decrease–increase trend with the change in concentration. A cell toxicity and acute oral toxicity experiment showed that the CnDDGPB surfactants were less toxic than the commonly used surfactant dodecyldimethylbenzyl ammonium chloride (1227). In addition, at a concentration of 150 ppm, CnDDGPB exhibited the same bacteriostatic effect as 1227 at a concentration of 100 ppm. The results demonstrate that sugar-based amide cationic surfactants are promising as environmentally friendly disinfection products.
- Open Access
- 31 January 2022
- Published by American Chemical Society (ACS) in ACS Omega
- Vol. 7 (6) , 5032-5038
Catalytic Performance of Li/Mg Composites for the Synthesis of Glycerol Carbonate from Glycerol and Dimethyl Carbonate
A series of Li/Mg composites were synthesized by the coprecipitation method using magnesium and lithium nitrates, and then used for the synthesis of glycerol carbonate (GC) from glycerol and dimethyl carbonate (DMC). The experimental results indicated that Li/Mg composites were prospective catalysts for GC synthesis. 92.05% glycerol conversion and 90.61% GC yield were obtained after reacting at 80 °C for 2 h in the presence of Li/Mg composites. The structure and properties of Li/Mg composites were characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Brunauer–Emmett–Teller (BET), and CO2–temperature-programmed desorption (TPD) techniques. It was inferred that the basic strength and basicity of Li/Mg composites were improved with increase in Li content. It was concluded that Li2CO3 was the main reactive species. A too-strong basic strength of Li/Mg composites could facilitate the glycerol conversion but impair GC selectivity.
- 31 January 2022
- Published by American Chemical Society (ACS) in ACS Omega
- Vol. 7 (6) , 5032-5038
Open AccessCatalytic Performance of Li/Mg Composites for the Synthesis of Glycerol Carbonate from Glycerol and Dimethyl Carbonate
A series of Li/Mg composites were synthesized by the coprecipitation method using magnesium and lithium nitrates, and then used for the synthesis of glycerol carbonate (GC) from glycerol and dimethyl carbonate (DMC). The experimental results indicated that Li/Mg composites were prospective catalysts for GC synthesis. 92.05% glycerol conversion and 90.61% GC yield were obtained after reacting at 80 °C for 2 h in the presence of Li/Mg composites. The structure and properties of Li/Mg composites were characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Brunauer–Emmett–Teller (BET), and CO2–temperature-programmed desorption (TPD) techniques. It was inferred that the basic strength and basicity of Li/Mg composites were improved with increase in Li content. It was concluded that Li2CO3 was the main reactive species. A too-strong basic strength of Li/Mg composites could facilitate the glycerol conversion but impair GC selectivity.