Salt-assisted thermal desorption of mercury from contaminated dredging sludge.

In this study, we tested a new procedure for the decontamination of mercury-polluted dredging sludge (Marano-Grado Lagoon, northeastern Italy) based on cationic exchange associated with thermal desorption at a low temperature. Four mercury-polluted sludge slurries were treated using thermal desorption at 393 K for 2h. Three different salts, NaCl (sodium chloride), (CH(3))(4)NCl (tetramethylammonium chloride) and (C(4)H(9))(4)NCl (tetrabutylammonium chloride) were used as exchangers. The selected salts have a monovalent cationic part that progressively increases in molecular weight. The results show that the association of cationic exchange with thermal treatment leads to a significant improvement in the removal of mercury from the contaminated material at a low temperature compared to samples that were not treated with salt. The highest levels of decontamination were attained were obtained when the slurries, which had mercury pollution ranging from 20 to 200 ppm, were treated with a 15% solution of (C(4)H(9))(4)NCl. The efficiency of the removal at 393 K (from 24% up to 60%) depended on the nature of the sample. When the samples were treated at a similar temperature without the salt, no remediation of mercury was detected. Our results show that the thermal decontamination temperature can be significantly lowered by this remediation approach, which is the first example based on cationic exchange of the pollutant with an appropriate salt.

Bench-scale tests on ultrasound-assisted acid washing and thermal desorption of mercury from dredging sludge and other solid matrices.

A series of ultrasonic assisted acid washing and thermal desorption tests were performed on sludge and other solid matrices with the aim to assay these removal technologies and to determine if the application of low frequency ultrasound was effective to enhance mercury removal. Unpolluted dredging sludge, 820 K calcinated dredging sludge, silica and alumina were characterized, polluted with a known concentration of mercury and treated both by acid washing and thermal desorption with and without low frequency ultrasound application. The acid washing was carried out by a 4% HNO(3) acid solution and the thermal desorption was performed in a 370-620K range. X-ray semi-quantitative analysis of dredging sludge before and after acid washing and granulometric curves of the matrices after the ultrasonic treatment were considered in order to evidence chemical or physical changes during these treatments. Total residual mercury measurements were carried out before and after sonication. Results showed not measurable acid washing extraction from polluted dredging sludge, a little (3%) extraction from 820K heat-treated sludge and a significant (10-20%) extraction from alumina and silica within 120 min of treatment. The ultrasound application gave generally poor improvement of the mercury removal. On the contrary thermal desorption of mercury was somewhat effective for alumina, silica and heat-treated dredging sludge samples in which mercury removal was 30-40% at 370 K and 90-99% at 570 K. Likewise ultrasound application did not improve desorption. Instead, the thermal treatment of dredging sludge had a negligible amount of mercury desorption at 370 K but it reached 95% at 570 K. The application of ultrasound improved the thermal extraction of 25% in the 470-520 K range of temperature.