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EC number: 266-019-3 | CAS number: 65996-85-2 The reaction product obtained by neutralizing coal tar oil alkaline extract with an acidic solution, such as aqueous sulfuric acid, or gaseous carbon dioxide, to obtain the free acids. Composed primarily of tar acids such as phenol, cresols, and xylenols.
- 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
Endpoint summary
Administrative data
Description of key information
Additional information
Biodegradation
Several biodegradation tests were performed under various conditions as well as following or according to standard methods.
Water - screening tests
Aerobic degradation was investigated in waste water, freshwater, seawater and anaerobic degradation was investigated with inoculum created from activated sludge.
Following concentrations were applied:
waste water, activated sludge - MITI I test: 100 mg/L
fresh water - BOD test: 3 - 10 mg/L
salt water - BOD test: 3 - 10 mg/L
anaerobic degradation - 1 - 5 mM
In all aerobic tests degradation rates > 70 % was achieved within in short period (< 10 d). In the anaerobic test 100 % biodegradation was achieved up to a concentration of 4 mM.
Out of the available tests only two standardised tests for ready biodegradability are available. In these MITI-I-tests, levels of degradation amounting to between 60 and 70 % (after 4 days) and to 85 % (after 14 days) were determined (Urano & Kato, 1986; MITI, 1992). With these results phenol can be classified as readily biodegradable. The results from the other available tests also points toward ready biodegradability. However, on account of the ubiquitous occurrence of phenol, adaptation is to be assumed in the case of all of the inocula. Since this also applies to WWTPs, a degradation rate constant of k = 1 h-1can be used for them.
Due to the high degradation rates within a period of < 10 days phenol is ready biodegradable in waste water, freshwater, sea water, and at anaerobic conditions with inoculum created from activated sludge.
Degradation by adapted microorganisms
In various degradation studies employing adapted microbial inocula (e.g. activated sludge from industrial wwtp) removal rates in the range of 98.5-100 % were demonstrated (BUA, 1997).
Water - simulation tests
In estuarine water samples the half-lives for the mineralisation of phenol were 7 days (k = 0.095/d) in summer and 73 days (k = 0.01/d) in winter, in the presence of sunlight. The authors could show however, that biodegradation was the primary removal process for phenol in both winter and summer. Calculating the arithmetic mean of the rate constants of 0.095/dand 0.01/d result in an average rate constant of 0.05/d, equivalent to a DT50 of 14 days. This value is in good agreement with the default rate constant of 0.047/d (DT50 15 days) proposed in the TGD for readily biodegradable substances.
Sediment
Simulation testing on degradation in sediment need not be conducted since the substance is readily biodegradable and direct and indirect exposure of sediment is unlikely.
However, as in the EU RAR (2006) in Section 3.1.2.1.1. the calculation of kbio sediment according to TGD using an experimental value for kbio soil of 0.1/d (DT50 soil 7 d) result in a rate constant for sediment of 0.01/d, equivalent to a DT50 of 69 days.
Biodegradation of phenol in sediment under anaerobic conditions was shown by several authors (supporting study of Horowitz et al., 1982). However, a longer adaptation phase than under aerobic conditions and therefore a slower degradation of phenol was found.
Soil
A rate constant for biodegradation of phenol in soils of ksoil = 0.1/d can be derived. from the available investigation of Haider et al. (1981) which corresponds to a DT50 of 7 days.
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