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Diss Factsheets
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EC number: 208-590-3 | CAS number: 534-16-7
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Particle size distribution (Granulometry)
Administrative data
Link to relevant study record(s)
- Endpoint:
- particle size distribution (granulometry)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 15 November 2007
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
- Remarks:
- Company data. Laser diffraction measurements of one representative commercial sample. Non-GLP
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 110 (Particle Size Distribution / Fibre Length and Diameter Distributions)
- Deviations:
- yes
- Remarks:
- Please refer to the assessment of reliability indicated above.
- Principles of method if other than guideline:
- No guideline specified, but comparable to OECD 110. A laser diffraction analysis has been carried out using the instrument Malvern Mastersizer 2000.
- GLP compliance:
- no
- Type of method:
- Laser scattering/diffraction
- Type of distribution:
- volumetric distribution
- Percentile:
- D10
- Mean:
- ca. 2.5 µm
- St. dev.:
- 0
- Percentile:
- D50
- Mean:
- ca. 7.5 µm
- St. dev.:
- 0
- Percentile:
- D90
- Mean:
- ca. 25.5 µm
- St. dev.:
- 0
- Conclusions:
- The particle size distribution of a typical commercial sample of silver carbonate is characterised by the following parameters: D10= ca. 2.5µm, D50=ca. 7.5 µm and D90 = ca. 25.5µm.
- Endpoint:
- particle size distribution (granulometry)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- test procedure in accordance with national standard methods
- Remarks:
- Test procedure in accordance with national standards DIN 55992-1:2006 ("Determination of a parameter for the dust formation of pigments and extenders - Part 1: Rotation method"), modified Heubach method
- Qualifier:
- according to guideline
- Guideline:
- other: DIN 55992-1:2006 (Determination of a parameter for the dust formation of pigments and extenders – Part 1: Rotation method)
- Deviations:
- yes
- Remarks:
- Please refer to rationale for reliability mentioned above.
- Principles of method if other than guideline:
- The Heubach dust meter is modified in a way that a seven stage cascade impactor is connected to the system. This involves an additional air fed of 20 L/min via the coarse dust separator needed to supply the cascade impactor with 40 L/min air current as specified in the manufacturer’s specifications.
The calculation report: (Klipsch, 2011)
The Multiple-Path Particle Dosimetry Model (MPPD, v2.0; CIIT, 2006) was used to predict this fractional deposition behaviour for workers.
The model algorithms calculate the deposition (and clearance) of mono-disperse and polydisperse aerosols in the respiratory tract for particles ranging from ultra-fine (0.01 microns) to coarse (20 microns) sizes. Within each airway, deposition is calculated using theoretically derived efficiencies for deposition by diffusion, sedimentation and impaction within the airway or airway bifurcation. Filtration of aerosols by the head is determined using empirical efficiency functions (for further information see "attached background material"). - GLP compliance:
- no
- Type of method:
- cascade impaction
- Type of distribution:
- volumetric distribution
- Percentile:
- other: MMAD 1 and GSD 1
- Mean:
- 0.52 µm
- St. dev.:
- 1.1
- Percentile:
- other: MMAD 2 and GSD 2
- Mean:
- 25.91 µm
- St. dev.:
- 2.93
- Remarks on result:
- not determinable
- Conclusions:
- Total Dustiness (airborne fraction): 59.45 mg/g (experimental results, DMT Report).
Mass median aerodynamic diameters (bi-modal distribution) of airborne fraction: MMAD1 = 0.52µm (1%) , MMAD2 = 25.91 µm (99%) (distribution fitted to Cascade impactor data, percentage in parentheses indicates weighting factor).
Geometric standard deviation of MMAD: GSD1 = 1.10, GSD 2 = 2.93.
Fractional deposition in human respiratory tract (MPPD model, based on calculated MMAD):
Head (ET): 49.31%
Tracheobronchial (TB): 0.48%
Pulmonary (PU): 0.73%
Referenceopen allclose all
Dustiness (airborne fraction): total: 59.45 mg/g.
In the original study report by DMT, a calculation of the mass median diameter was not conducted. Since the deposited fractions were provided for each of the cascade impactor stages, it was possible to fit a bi-modal lognormal distribution to the data by standard non-linear regression procedure. As a result, the MMAD and GSD are calculable and reported: p1: 1%, MMAD1 = 0.52 µm, GSD1 = 1.10 / p2: 99%, MMAD 2 = 25.91 µm, GSD2 = 2.93
As the cascade impactor already takes aerodynamic characteristics of the particles into account, the reported mass median diameter can be interpreted as the mass medianaerodynamicdiameter.
This figure and the corresponding GSD were used as distribution parameters for the MPPD model enabling an estimation of deposited dust fractions in the human respiratory tract: These fractions were estimated as follows:
Head (ET): 49.31%
Tracheobronchial (TB): 0.48%
Pulmonary (PU): 0.73%
Description of key information
The particle size distribution of a representative commercial sample of silver(I)carbonate is characterised by the following parameters (mass/volume-based distribution): D10 = ca. 2.5 µm, D50 = ca. 7.5 µm, D90 = ca. 25.5 µm.
In a laboratory test for dustiness (rotating drum), simulating conditions of physical agitation of the material, approx. 60 mg/g (i.e. ca. 6% of the mass of the material) became airborne. The mass median diameter (MMAD) of the airborne material was determined at ca. 26 µm. Using a multiple path particle dosimetry model (MPPD), the fractional deposition of inhaled material in the human lung was estimated as follows: head-region: 49.31%, tracheobronchial-region: 0.48%, pulmonary-region: 0.73%. The balance to 100%, i.e. 49.48% of airborne material are considered not to be inhalable.
Additional information
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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