Qiaohong Zhang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Qiaohong Zhang has a total of 52 co-authors. Here are the top co-authors by number of shared publications:
- Chen Chen
State Key Laboratory Base of Novel Functional Materials and Preparation Science, School of Materials Science & Chemical Engineering, Ningbo University, Ningbo, China
4 shared publications Chen Chen
3 shared publicationsDezhong Xie
2 shared publicationsFengkuan Ma
2 shared publicationsGuoying Weng
State Key Laboratory Base of Novel Functional Materials and Preparation Science, School of Materials Science & Chemical Engineering, Ningbo University, Ningbo, China
2 shared publicationsHuibin Wang
2 shared publications
Latest Publications
- 1 January 2026
- Published by Shanghai Institute of Organic Chemistry in Acta Chimica Sinica
- Vol. 84 (4) , 471
Catalytic Decomposition of Alkyl Hydroperoxides with Ferrous Salt under the Visible Light at Ambient Temperature
- 1 January 2026
- Published by Shanghai Institute of Organic Chemistry in Acta Chimica Sinica
- Vol. 84 (4) , 471
Catalytic Decomposition of Alkyl Hydroperoxides with Ferrous Salt under the Visible Light at Ambient Temperature
- 9 November 2023
- Published by American Chemical Society (ACS) in ACS Applied Nano Materials
- Vol. 6 (22) , 21123-21132
Ultradeep Removal of Acetaldehyde from Ethanol through Catalytic Hydrogenation with Highly Dispersed Ag Nanoparticles Supported on Phenyl-Modified SiO2
- 9 November 2023
- Published by American Chemical Society (ACS) in ACS Applied Nano Materials
- Vol. 6 (22) , 21123-21132
Ultradeep Removal of Acetaldehyde from Ethanol through Catalytic Hydrogenation with Highly Dispersed Ag Nanoparticles Supported on Phenyl-Modified SiO2
- 28 August 2023
- Published by Elsevier in Molecular Catalysis
- Vol. 549
Catalytic oxidation of hydrocarbon with the organic metal-free system of N-hydroxyphthalimide/tert‑butyl nitrite at room temperature
- 28 August 2023
- Published by Elsevier in Molecular Catalysis
- Vol. 549
Catalytic oxidation of hydrocarbon with the organic metal-free system of N-hydroxyphthalimide/tert‑butyl nitrite at room temperature
- 26 September 2022
- Published by Elsevier in Applied Surface Science
- Vol. 607, 154942
NH2-SiO2-C3H7 with abundant surface groups exposure as the efficient catalyst for the Aldol condensation reaction
- 26 September 2022
- Published by Elsevier in Applied Surface Science
- Vol. 607, 154942
NH2-SiO2-C3H7 with abundant surface groups exposure as the efficient catalyst for the Aldol condensation reaction
- 1 November 2021
- Published by Elsevier in International Journal of Hydrogen Energy
- Vol. 46 (79) , 39251-39261
A 3D flower-like WC with large capacitance as efficient co-catalyst in photocatalytic H2 evolution
- 1 November 2021
- Published by Elsevier in International Journal of Hydrogen Energy
- Vol. 46 (79) , 39251-39261
A 3D flower-like WC with large capacitance as efficient co-catalyst in photocatalytic H2 evolution
- 5 October 2021
- Published by Wiley in Advanced Functional Materials
- Vol. 32 (2) , 2106828
Synthesis of Amphiphilic Silica with High Exposure of Surface Groups and Its Utilization in Efficient Removal of Organic Dyes from Aqueous Solution
Amphiphilic silica is synthesized with the simultaneous introduction of two kinds of polar and weakly polar organic groups on its surface using a one‐step reverse‐phase microemulsion method. The obtained materials present as nanospheres with a size of ≈100 nm. A high percentage (≈80%) of silicon species can be exposed and the amount of surface SiOH increased by above 50% with the introduction of organic groups. Plenty of groups, including polar groups (3‐aminopropyl and hydroxyl) and weakly polar group (n‐propyl) coexisting on the surface, enable the material to show amphiphilicity. This amphiphilic material can show an excellent property for the removal of various organic dyes from the aqueous solution, and the maximum adsorption capacity of Congo Red, Acid Blue 25, Reactive Blue 19, and Reactive Black 5 can reach 2453.1, 1157.7, 964.6, and 916.9 mg g−1, respectively. Good reusability is also realized for the present amphiphilic material, which can be reused for at least three times. The reported work provides a successful example to prove that the surface hydrophilicity and lipophilicity can be simultaneously improved just through a simple introduction of certain organic groups, and then realize efficient removal of dyes from the polluted water.
- 5 October 2021
- Published by Wiley in Advanced Functional Materials
- Vol. 32 (2) , 2106828
Synthesis of Amphiphilic Silica with High Exposure of Surface Groups and Its Utilization in Efficient Removal of Organic Dyes from Aqueous Solution
Amphiphilic silica is synthesized with the simultaneous introduction of two kinds of polar and weakly polar organic groups on its surface using a one‐step reverse‐phase microemulsion method. The obtained materials present as nanospheres with a size of ≈100 nm. A high percentage (≈80%) of silicon species can be exposed and the amount of surface SiOH increased by above 50% with the introduction of organic groups. Plenty of groups, including polar groups (3‐aminopropyl and hydroxyl) and weakly polar group (n‐propyl) coexisting on the surface, enable the material to show amphiphilicity. This amphiphilic material can show an excellent property for the removal of various organic dyes from the aqueous solution, and the maximum adsorption capacity of Congo Red, Acid Blue 25, Reactive Blue 19, and Reactive Black 5 can reach 2453.1, 1157.7, 964.6, and 916.9 mg g−1, respectively. Good reusability is also realized for the present amphiphilic material, which can be reused for at least three times. The reported work provides a successful example to prove that the surface hydrophilicity and lipophilicity can be simultaneously improved just through a simple introduction of certain organic groups, and then realize efficient removal of dyes from the polluted water.
- 1 October 2021
- Published by Elsevier in Journal of Chromatography A
- Vol. 1655, 462505
Graphene functionalized with structurally complementary amino acids for sensitive recognition of N-linked glycopeptides
- 1 October 2021
- Published by Elsevier in Journal of Chromatography A
- Vol. 1655, 462505
Graphene functionalized with structurally complementary amino acids for sensitive recognition of N-linked glycopeptides