scholarly journals Facile Preparation Carbon-Doped TiO$lt;inf$gt;2$lt;/inf$gt; Nanotube Electrodes and Its Enhanced Photoelectrochemical Response

2015 ◽  
Vol 30 (6) ◽  
pp. 599
Author(s):  
ZHAO Peng ◽  
LI Zhong ◽  
CUI Xiao-Li
Keyword(s):  
Carbon Doped ◽  
Photoelectrochemical Response ◽  
Facile Preparation

MAGNETIC ANISOTROPY OF CARBON DOPED Nd2Fe14B

1985 ◽  
Vol 46 (C6) ◽  
pp. C6-305-C6-308 ◽  
Author(s):  
F. Bolzoni ◽  
F. Leccabue ◽  
L. Pareti ◽  
J. L. Sanchez
Keyword(s):  
Magnetic Anisotropy ◽  
Carbon Doped

Facile preparation of nanofiller-paper using mixed office paper without deinking

TAPPI Journal ◽  
2015 ◽  
Vol 14 (3) ◽  
pp. 167-174 ◽  
Author(s):  
QIANQIAN WANG ◽  
J.Y. ZHU
Keyword(s):  
Cellulose Nanofibrils ◽  
Ash Content ◽  
Raw Material ◽  
Mechanical Grinding ◽  
Microscope Imaging ◽  
Facile Preparation ◽  
Electron Microscope Imaging ◽  
Thermal Stability Of ◽  
Scanning Electron ◽  
Office Paper

Mixed office paper (MOP) pulp without deinking with an ash content of 18.1 ± 1.5% was used as raw material to produce nanofiller-paper. The MOP pulp with filler was mechanically fibrillated using a laboratory stone grinder. Scanning electron microscope imaging revealed that the ground filler particles were wrapped by cellulose nanofibrils (CNFs), which substantially improved the incorporation of filler into the CNF matrix. Sheets made of this CNF matrix were densified due to improved bonding. Specific tensile strength and modulus of the nanofiller-paper with 60-min grinding reached 48.4 kN·m/kg and 8.1 MN·m/kg, respectively, approximately 250% and 200% of the respective values of the paper made of unground MOP pulp. Mechanical grinding duration did not affect the thermal stability of the nanofiller-paper.

Thienopyrrolocarbazoles: New Building Blocks for Functional Organic Materials

2019 ◽  
Author(s):  
Dorian Bader ◽  
Johannes Fröhlich ◽  
Paul Kautny
Keyword(s):  
Building Block ◽  
Organic Materials ◽  
Building Blocks ◽  
Molecular Properties ◽  
The Family ◽  
Facile Preparation

The facile preparation of three regioisomeric thienopyrrolocarbazoles applying a convenient C-H activation approach is presented. Derived from indolo[3,2,1-<i>jk</i>]carbazole, the incorporation of thiophene into the triarylamine framework significantly impacted the molecular properties of the parent scaffold. The developed thienopyrrolocarbazoles enrich the family of triarylamine donors and constitute a novel building block for functional organic materials.

Thienopyrrolocarbazoles: New Building Blocks for Functional Organic Materials

2019 ◽  
Author(s):  
Dorian Bader ◽  
Johannes Fröhlich ◽  
Paul Kautny
Keyword(s):  
Building Block ◽  
Organic Materials ◽  
Building Blocks ◽  
Molecular Properties ◽  
The Family ◽  
Facile Preparation

The facile preparation of three regioisomeric thienopyrrolocarbazoles applying a convenient C-H activation approach is presented. Derived from indolo[3,2,1-<i>jk</i>]carbazole, the incorporation of thiophene into the triarylamine framework significantly impacted the molecular properties of the parent scaffold. The developed thienopyrrolocarbazoles enrich the family of triarylamine donors and constitute a novel building block for functional organic materials.

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