Facile synthesis of direct sunlight-driven anatase TiO2 nanoparticles by in situ modification with trifluoroacetic acid

2012 ◽  
Vol 14 (10) ◽  
Author(s):  
Xiangfu Meng ◽  
Lin Qi ◽  
Zhichang Xiao ◽  
Shuyan Gong ◽  
Qingli Wei ◽  
...  
CrystEngComm ◽  
2015 ◽  
Vol 17 (36) ◽  
pp. 6868-6877 ◽  
Author(s):  
Jian-Li Mi ◽  
Kirsten M. Ø. Jensen ◽  
Christoffer Tyrsted ◽  
Martin Bremholm ◽  
Bo B. Iversen

The in situ PDF method provides detailed information about the formation and growth mechanisms of TiO2 anatase nanoparticles under hydrothermal conditions.


2020 ◽  
Vol 2 (4) ◽  
Author(s):  
G. Nagaraj ◽  
D. Brundha ◽  
C. Chandraleka ◽  
M. Arulpriya ◽  
V. Kowsalya ◽  
...  

2018 ◽  
Vol 33 (10) ◽  
pp. 1136
Author(s):  
JIANG Feng ◽  
YU Yun ◽  
FENG Ai-Hu ◽  
YU Yang ◽  
MI Le ◽  
...  

1992 ◽  
Vol 45 (8) ◽  
pp. 1225 ◽  
Author(s):  
G Tong ◽  
JW Perich ◽  
RB Johns

The improved synthesis of Boc -L-Abu(PO3Me2)-OH from Boc-Asp-Obut in 42% overall yield is described. This derivative was prepared in seven steps and involved initial sodium borohydride reduction of the isobutoxycarbonyl mixed anhydride of BOC-Asp-OBut and subsequent 2,2,6,6- tetramethylpiperidine-1-oxyl-catalysed sodium hypochlorite oxidation of the alcohol. The resultant aldehyde was phosphonylated by reflux with dimethyl trimethylsilyl phosphite and the trimethylsilyl group was then cleaved in situ by aqueous hydrolysis. The 4-hydroxy 4-dimethylphosphono derivative was converted into the Abu(PO3Me2) residue by reaction with thiocarbonyldiimidazole followed by radical deoxygenation of the thiocarbonylimidazolide with tributyltin hydride. The Boc and t-butyl groups were cleaved from BOC-Abu(PO3Me2)-OBut with trifluoroacetic acid and the Boc group was reintroduced to CF3CO2H.H-Abu(PO2Me2)-OH by using di-t-butyl dicarbonate to give Boc -Abu(PO3Me2)-OH as a clear oil. The optical purity of the Abu(PO3Me2) residue was established to be greater than 99.5% of the L-isomer by h.p.1.c. analysis of its L- Leu dipeptide. The protected derivative Boc-Abu(PO3Me2)-OH was used in the Boc mode of peptide synthesis for the preparation of Boc-Glu (OBz1)-Abu(PO3Me2)-Leu-OBzl in high yield, 40% CF3CO2H/CH2Cl2 being used for cleavage of the Boc group from intermediate peptides. The tripeptide was deprotected to CF3CO2H.H-Glu-Abu(P)- Leu -OH by a two-step procedure which involved initial hydrogenolytic cleavage of the benzyl groups in 50% CF3CO2H/CH3CO2H followed by cleavage of the methyl phosphate groups with either (A) 30% bromotrimethylsilane in acetonitrile, or (B) 1 M bromotrimethylsilane /l M thioanisole in trifluoroacetic acid; complete cleavage of the methyl groups was effected after 40 min and 12 h, respectively. In addition, the dipeptide Boc-Leu-Abu (P03Me2)- OBut was prepared from Boc-Abu(PO3Me2)-OBut in high yield and was readily deprotected by acidolytic cleavage of the t-butyl groups with trifluoroacetic acid followed by silylitic cleavage of the methyl phosphonate groups with 30% bromotrimethylsilane in acetonitrile, CF3CO2H.H-Leu-Abu(P)-OH being obtained in high yield.


2019 ◽  
Vol 75 (a2) ◽  
pp. e643-e643
Author(s):  
Frederik Søndergaard-Pedersen ◽  
Nils Lau Nyborg Broge ◽  
Jinlong Yu ◽  
Aref Mamakhel ◽  
Jonas Beyer ◽  
...  

Nanoscale ◽  
2013 ◽  
Vol 5 (6) ◽  
pp. 2372 ◽  
Author(s):  
Jakob Rostgaard Eltzholtz ◽  
Christoffer Tyrsted ◽  
Kirsten Marie Ørnsbjerg Jensen ◽  
Martin Bremholm ◽  
Mogens Christensen ◽  
...  

2020 ◽  
Vol 35 (2) ◽  
pp. 221-228
Author(s):  
S.-B. Chen ◽  
T.-X. Li ◽  
S.-H. Wan ◽  
X. Huang ◽  
S.-W. Cai ◽  
...  

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 272
Author(s):  
Ayman M. Atta ◽  
Mohamed H. El-Newehy ◽  
Meera Moydeen Abdulhameed ◽  
Mohamed H. Wahby ◽  
Ahmed I. Hashem

The enhancement of both thermal and mechanical properties of epoxy materials using nanomaterials becomes a target in coating of the steel to protect it from aggressive environmental conditions for a long time, with reducing the cost. In this respect, the adhesion properties of the epoxy with the steel surfaces, and its proper superhyrophobicity to repel the seawater humidity, can be optimized via addition of green nanoparticles (NPs). In-situ modification of silver (Ag) and calcium carbonate (CaCO3) NPs with oleic acid (OA) was carried out during the formation of Ag−OA and CaCO3−OA, respectively. The epoxide oleic acid (EOA) was also used as capping for Ca−O3 NPs by in-situ method and epoxidation of Ag−OA NPs, too. The morphology, thermal stability, and the diameters of NPs, as well as their dispersion in organic solvent, were investigated. The effects of the prepared NPs on the exothermic curing of the epoxy resins in the presence of polyamines, flexibility or rigidity of epoxy coatings, wettability, and coatings durability in aggressive seawater environment were studied. The obtained results confirmed that the proper superhyrophobicity, coating adhesion, and thermal stability of the epoxy were improved after exposure to salt spray fog for 2000 h at 36 °C.


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