Lactone radical transformed methyl mercaptan-adsorbed activated carbon into graphene oxide modified activated carbon.

Activated carbon was a widely-used adsorbent. However, it was usually classified as a hazardous waste after saturation adsorption for one pollution. For the first time, this article reported a regeneration method for the activated carbon saturated with methyl mercaptan. The regenerated carbon was partially transformed into graphene-oxide fragment with a thickness of 0.9-1.0 nm after a hydrothermal treatment at 180 °C. Electron paramagnetic resonance revealed that lactone group was transformed into lactone radical under the hydrothermal condition. The spins were increased from 4.54E+17-1.24E+18. The formed radical effectively reacted with the adsorbed methyl mercaptan and re-distributed the amorphous activated carbon to form lamellar graphene oxide. As a result, the spins were decreased from 1.24E+18-8.73E+17. At the same time, the amount of lactone group was decreased from 0.71 to 0.42 mmol/g. The regenerated activated carbon thus regained ability to adsorb methyl mercaptan. The main result of this paper puts forward a simple and low-cost method to obtain graphene oxide modified activated carbon from the regeneration of hazardous waste carbon. This conclusion makes contribution to the development of "zero-waste" conception.

Fixation stability of glass matrix co-existent with crystal phases for heavy metals formed by high-temperature vitrification.

Vitrification is an effective solidification method for heavy metal-containing wastes. However, most investigations focused on the formation of glass matrix. Seldom report discussed the influence of co-existing crystals on heavy metal stabilizations. In this work, Ca-Al-Si phase was formed in the glass matrix by adjusting the composition of feeding ingredient and melting temperature. As a result, when molar ratio of CaO/(SiO2+Al2O3) was lower than 0.97 and reaction temperature was bigger than 1300 °C, small-size Ca-Al-Si phase (Ca2Al2SiO7 and CaAl2Si2O8) was homogeneously distributed in vitreous matrix. At the same time, Cr, Zn, and Pb leaching concentrations were the lowest, far lower than the leaching standard values. According to theoretical calculations, Zn and Pb replaced Ca atom; Cr replaced Al atom in Ca-Al-Si phase under thermal conditions. These replacements resulted in the fixation and stabilization of heavy metals. When the CaO/(SiO2+Al2O3) molar ratio was bigger than 1.00, neither glass nor Ca-Al-Si was formed. Similarly, when the melting temperature was decreased, Ca-Al-Si phase formed a bigger size. Both these went against the stabilization, resulting in high leaching concentrations of heavy metals. The main of this work will help the development of high-temperature melting for the treatment of hazardous wastes.

[Adsorption of a dye by sludges and the roles of extracellular polymeric substances].

This paper investigated the adsorption of a dye, acid turquoise blue A, by four kinds of sludges including activated sludge, anaerobic sludge, dried activated sludge, and dried anaerobic sludge, respectively. The roles of extracellular polymeric substances (EPS) including the soluble EPS (SEPS) and bound EPS (BEPS) for the biosorption of activated sludge and anaerobic sludge were further studied. Results show that the relation between four kinds of sludge adsorption amount and remained concentration of the dye fitted well both Freundlich model (R2: 0.921-0.995) and Langmuir model (R2: 0.958-0.993), but not quite fitted BET model (R2: 0.07-0.863). The adsorption capability of dried anaerobic sludge ranked the highest, and dried activated sludge was the lowest. According to Langmuir isotherm, the maximum adsorption amount of dried anaerobic, anaerobic, activated, and dried activated sludge was 104 mg/g, 86 mg/g, 65 mg/g, 20 mg/g, respectively. The amount of the dye found in EPS for both activated sludge and anaerobic sludge were over 50%, illustrating that EPS adsorption was predominant in adsorption of the dye by sludge. The amount of adsorbed dye by BEPS was greater than that by SEPS for anaerobic sludge, but for activated sludge the result was quite opposite. The amount of adsorbed dye by unit mass SEPS was much higher than the corresponding values of BEPS for both sludges. The average amount of adsorbed dye by unit mass SEPS was 52 times of the corresponding value of BEPS for activated sludge, and 10 times for anaerobic sludge. The relation between adsorption amount of dye by BEPS from anaerobic sludge and remained concentration of the dye in mixed liquor was best fitted to Langmuir model (R2: 0.9986).