Flame synthesis of calcium carbonate nanoparticles
Literature Information
Matthias Huber, Wendelin J. Stark, Stefan Loher, Marek Maciejewski, Frank Krumeich, Alfons Baiker
Calcium carbonate nanoparticles of 20–50 nm size were obtained from a flame spray process where combustion of specific calcium-containing precursors results in amorphous or crystalline calcium carbonate particles depending on the spray flow conditions.
Recommended Journals
Related Literature
Sandwich-type Na6B7− and Na8B7+ clusters: charge-transfer complexes, four-fold π/σ aromaticity, and dynamic fluxionality
Lin-Yan Feng, Hua-Jin Zhai
DOI: 10.1039/C9CP03611C
Elucidating the structure and dynamics of CO ad-layers on MgO surfaces
Jefferson Maul, Giuseppe Spoto, Lorenzo Mino, Alessandro Erba
DOI: 10.1039/C9CP05418A
Polypyrrole derivatives for optoelectronic applications: a DFT study on the influence of side groups
Alex Pifer Coleone, Leonardo Gois Lascane
DOI: 10.1039/C9CP02638J
Replica exchange MD simulations of two-dimensional water in graphene nanocapillaries: rhombic versus square structures, proton ordering, and phase transitions
Shujuan Li, Burkhard Schmidt
DOI: 10.1039/C9CP00849G
Mechanism and theory of d-glucopyranose homogeneous acid catalysis in the aqueous solution phase
Karla Dussan
DOI: 10.1039/C8CP07224H
Multiscale landscape of molecular mechanism of SIRT1 activation by STACs
Fei Liu, Na Yang
DOI: 10.1039/C9CP04931B
Enhanced anisotropic electrical conductivity of perturbed monolayer β12-borophene
Nguyen N. Hieu, Bui Dinh Hoi
DOI: 10.1039/C9CP05597E
Comment on “Penicillin’s catalytic mechanism revealed by inelastic neutrons and quantum chemical theory” by Z. Mucsi, G. A. Chass, P. Ábrányi-Balogh, B. Jójárt, D.-C. Fang, A. J. Ramirez-Cuesta, B. Viskolczc and I. G. Csizmadia, Phys. Chem. Chem. Phys., 2013, 15, 20447
DOI: 10.1039/C8CP02413H
Theoretical investigation of the valence states in Au via the Au–F compounds under high pressure
Guangtao Liu, Linyan Wang, Xue Yong, Guoying Gao, Hanyu Liu
DOI: 10.1039/C9CP02409C
About the origin of the large Stokes shift in aminoalkyl substituted heptamethine cyanine dyes
Cristina Sissa, Anna Painelli, Francesca Terenziani, Massimo Trotta, Roberta Ragni
DOI: 10.1039/C9CP05473A
You might also like
What precautions should be taken when handling 4-Methyl-6-(trifluoromethyl)quinoline (CAS: 40716-16-3)?
When handling 4-Methyl-6-(trifluoromethyl)quinoline (CAS: 40716-16-3), safety go...
What is 4-(3,5-Difluorophenyl)aniline (CAS: 405058-00-6)?
4-(3,5-Difluorophenyl)aniline is an aromatic organic compound with the CAS numbe...
How is 5-{[4-(Trifluoromethyl)phenyl]sulfanyl}-1,2,3-thiadiazole-4-carboxylic acid (CAS: 338982-07-3) typically synthesized?
5-{[4-(Trifluoromethyl)phenyl]sulfanyl}-1,2,3-thiadiazole-4-carboxylic acid can ...
What is the market or research trend for 4-Benzylaniline hydrochloride (CAS: 6317-57-3)?
The market for 4-Benzylaniline hydrochloride (CAS: 6317-57-3) is steadily growin...
Is [3-(Diethylsulfamoyl)phenyl]boronic acid (CAS: 871329-58-7) safe?
[3-(Diethylsulfamoyl)phenyl]boronic acid is generally considered safe when handl...
What are the main uses of 3-Bromo-2,5-dimethoxyaniline (CAS: 115929-62-9)?
3-Bromo-2,5-dimethoxyaniline is mainly used in the pharmaceutical and chemical i...
What regulatory guidelines apply to N-Methyl-1-(5-methyl-1H-indol-3-yl)methanamine (CAS: 915922-67-7)?
N-Methyl-1-(5-methyl-1H-indol-3-yl)methanamine (CAS: 915922-67-7) is subject to ...
What industries use Carbamic acid, N-[(5S)-5,6-diamino-6-oxohexyl]-, 1,1-dimethylethyl ester (CAS: 24828-96-4)?
This compound is primarily used in the pharmaceutical industry for the synthesis...
How should 2-Methyl-2-propanyl [(1S,3R)-3-aminocyclohexyl]carbamate (CAS: 1298101-47-9) be stored?
2-Methyl-2-propanyl [(1S,3R)-3-aminocyclohexyl]carbamate (CAS: 1298101-47-9) sho...
What industries use Ethyl 2-bromo-4,4,4-trifluorobutanoate (CAS: 367-33-9)?
Ethyl 2-bromo-4,4,4-trifluorobutanoate (CAS: 367-33-9) is utilized in the pharma...
Source Journal
Chemical Communications

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry













![2,4-Dichloro-6-isopropyl-5H-pyrrolo[3,4-d]pyrimidin-7(6H)-one structure 2,4-Dichloro-6-isopropyl-5H-pyrrolo[3,4-d]pyrimidin-7(6H)-one structure](https://static.chemtradehub.com/structs/107/1079649-94-7-ad4a.webp)
