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Diss Factsheets

Physical & Chemical properties

Nanomaterial crystalline phase

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Administrative data

Endpoint:
nanomaterial crystalline phase
Remarks:
NC7000 XRD
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
accepted calculation method

Data source

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
- Principle of test: X-Ray difffraction
- Short description of test conditions: The diffractogram was acquired in θ/2θ mode using the Cu Kα radiation (λ = 1,5406 nm).
The angular range scan ranged from 10° to 60°, with an angular step of 0.016° and an acquisition time of 1 s.
- Parameters analysed / observed:
GLP compliance:
no
Type of method:
x-ray diffraction (XRD)
Details on methods and data evaluation:
The diffraction pattern of the powder was recorded. No additional modification was performed on the recorded diagram.
Sampling:
Preparation of test samples and references (including the use of energy and dispersants):
The CNT sample was first grinded into a very fine powder using a mortar and pestle, then it was dispersed in a uniform layer on an amorphous silica plate using pure ethanol.
After complete drying the sample was positioned in the goniometer of the apparatus.

Test material

Constituent 1
Chemical structure
Reference substance name:
carbon
EC Number:
936-414-1
Molecular formula:
C
IUPAC Name:
carbon
Test material form:
solid: nanoform, no surface treatment
Details on test material:
- State of aggregation: entangled nanotubes, as described in Section 4.28.1
- Particle size distribution: entangled nanotubes, as described in Section 1.2, 1.4. and 4.28.1.
- Mass median aerodynamic diameter (MMAD): As the product tends to agglomerate this depends on the testing conditions. See Section 4.
- Geometric standard deviation (GSD): Depends on the testing conditions. See Section 4.
- Shape of particles:nanotubes, aspect ratio of ~163:1
- Surface area of particles: 250 - 300 m²/g (BET)
- Crystal structure: graphite.
- Coating: None
- Surface properties: No functionalization intended.
- Density: May vary depending on the batch number. Available information is reported in the Confidential details on test material for each study.
- Moisture content: Not determined. May vary depending on the batch number.
- Residual solvent: Not applicable.
- Activation: Not applicable.
- Stabilisation: Not applicable.
- Other: Not applicable.

Data gathering

Instruments:
The diffraction pattern of the powder was recorded on a D8 ADVANCE apparatus (BRUKER) equipped with a Vantec detector.

Results and discussion

Crystalline phase
Key result
Common name:
graphite
Crystallographic composition:

The multi-walled carbon nanotubes present graphite like structure, identified by X-ray diffraction. Typical X-ray diffraction spectra are presented hereafter. They clearly show the presence of interlayer spacing similar to those of graphite (two main rays at 2θ= about 25 and about 44) as well as rays corresponding to the hexagonal arrangements.

Applicant's summary and conclusion

Conclusions:
The multi-walled carbon nanotubes present graphite like structure, identified by X-ray diffraction. Typical X-ray diffraction spectra clearly show the presence of interlayer spacing similar to those of graphite (two main rays at 2θ = about 25 and about 44) as well as rays corresponding to the hexagonal arrangements.
Executive summary:

The multi-walled carbon nanotubes present graphite like structure identified by X-ray diffraction.