Hongyun Hu

Emission characteristics of nitrogen- and sulfur-containing odorous compounds during different sewage sludge chemical conditioning processes

Chemical conditioners are often used to enhance sewage sludge dewaterability through altering sludge properties and flocs structure, both affect odorous compounds emissions not only during sludge conditioning but also in subsequent sludge disposal. This study was to investigate emission characteristics of ammonia (NH(3)), sulfur dioxide (SO(2)), hydrogen sulfide (H(2)S) and carbonyl sulfide (COS) generated from sewage sludge conditioned by three representative conditioners, i.e., organic polymers, iron salts and skeleton builders, F-S (Fentons reagent and skeleton builders) composite conditioner. The results demonstrate that polyacrylamide (PAM) has an insignificant effect on emission characteristics of nitrogen- and sulfur-containing odorous compounds, because the properties, sulfur and nitrogen speciations are similar in PAM-conditioned sludge and raw sludge (RS). Significant increases of SO(2) and H(2)S emissions in the H(2)SO(4) conditioning process were observed due to the accelerated decomposition of sulfur-containing amino acids in acidic environment. Fenton peroxidation facilitates the formation of COS. CaO can reduce sulfur-containing gases emission via generation of calcium sulfate. However, under strong alkaline conditions, free ammonia or protonated amine in sludge can be easily converted to volatile ammonia, resulting in a significant release of NH(3).

Comparison of CaO’s effect on the fate of heavy metals during thermal treatment of two typical types of MSWI fly ashes in China

Both grate and fluidized bed incinerators are widely used for MSW incineration in China. CaO addition for removing hazardous emissions from MSWI flue gas changes the characteristics of fly ash and affects the thermal behavior of heavy metals when the ash is reheated. In the present work, two types of MSWI fly ashes, sampled from both grate and fluidized bed incinerators respectively, were thermal treated at 1023-1323 K and the fate of heavy metals was observed. The results show that both of the fly ashes were rich in Ca and Ca-compounds were the main alkaline matter which strongly affected the leaching behavior of heavy metals. Ca was mostly in the forms of Ca(OH)2 and CaCO3 in the fly ash from grate incinerator in which nascent fly ash particles were covered by Ca-compounds. In contrast, the content of Ca was lower in the fly ash from fluidized bed incinerator and Ca was mostly in the form of CaSO4. Chemical reactions among Ca-compounds caused particle agglomeration in thermal treated fly ash from grate incinerator, restraining the heavy metals volatilization. In thermal treated fly ash from fluidized bed incinerator, Ca was converted into aluminosilicates especially at 1323 K which enhanced heavy metals immobilization, decreasing their volatile fractions as well as leaching concentrations. Particle agglomeration hardly affected the leaching behavior of heavy metals. However, it suppressed the leachable-CaCrO4 formation and lowered Cr leaching concentration.

CO2 co-gasification of lower sulphur petroleum coke and sugar cane bagasse via TG–FTIR analysis technique

This study investigates the non-isothermal mechanism and kinetic behaviour of gasification of a lower sulphur petroleum coke, sugar cane bagasse and blends under carbon dioxide atmosphere conditions using the thermogravimetric analyser (TGA). The gas products were measured online with coupled Fourier transform infrared spectroscopy (FTIR). The achieved results explored that the sugar cane bagasse and blend gasification happened in two steps: at (<500 °C) the volatiles are released, and at (>700 °C) char gasification occurred, whereas the lower sulphur petroleum coke presented only one char gasification stage at (>800 °C). Significant interactions were observed in the whole process. Some solid-state mechanisms were studied by the Coats-Redfern method in order to observe the mechanisms responsible for the gasification of samples. The results show that the chemical first order reaction is the best responsible mechanism for whole process. The main released gases are CO2, CO, CH4, HCOOH, C6H5OH and CH3COOH.

The fate of sulfur during rapid pyrolysis of scrap tires

The fate of sulfur during rapid pyrolysis of scrap tires at temperatures from 673 to 1073K was investigated. Sulfur was predominant in the forms of thiophenic and inorganic sulfides in raw scrap tires. In the pyrolysis process, sulfur in organic forms was unstable and decomposed, leading to the sulfur release into tar and gases. At 673 and 773K, a considerable amount of sulfur was distributed in tar. Temperature increasing from 773 to 973K promoted tar decomposition and facilitated sulfur release into gases. At 1073K, the interactions between volatiles and char stimulated the formation of high-molecular-weight sulfur-containing compounds. After pyrolysis, almost half of the total content of sulfur in raw scrap tires still remained in the char and was mostly in the form of sulfides. Moreover, at temperatures higher than 873K, part of sulfur in the char was immobilized in the sulfates. In the pyrolysis gases, H2S was the main sulfur-containing gas. Increasing temperature stimulated the decomposition of organic polymers in scrap tires and more H2S was formed. Besides H2S, other sulfur-containing gases such as CH3SH, COS and SO2 were produced during the rapid pyrolysis of scrap tires.

Combined effects of Fenton peroxidation and CaO conditioning on sewage sludge thermal drying

Joint application of Fentons reagent and CaO can dramatically enhance sludge dewaterability, thus are also likely to affect subsequent thermal drying process. This study investigated the synergistic effects of the two conditioners on the thermal drying behavior of sewage sludge and the emission characteristics of main sulfur-/nitrogen-containing gases. According to the results, Fenton peroxidation combined with CaO conditioning efficiently promoted sludge heat transfer, reduced the amounts of both free and bound water, and created porous structure in solids to provide evaporation channels, thus producing significant positive effects on sludge drying performance. In this case, the required time for drying was shortened to one-third. Additionally, joint usage of Fentons reagent and CaO did not increase the losses of organic matter during sludge drying process. Meanwhile, they facilitated the formation of sulfate and sulfonic acid/sulfone, leading to sulfur retention in dried sludge. Both of Fenton peroxidation and CaO conditioning promoted the oxidation, decomposition, and/or dissolution of protein and inorganic nitrogen in sludge pre-treatment. As a consequence, the emissions of sulfurous and nitrogenous gases from dewatered sludge drying were greatly suppressed. These indicate that combining Fenton peroxidation with CaO conditioning is a promising strategy to improve drying efficiency of sewage sludge and to control sulfur and nitrogen contaminants during sludge thermal drying process.

Correlations between hydrochar properties and chemical constitution of orange peel waste during hydrothermal carbonization

For efficient hydrothermal treatment of biomass, this study aims to figure out the correlations between complex chemical constitution of orange peel (OraPeel) as typical bio-waste and the physicochemical structure of its derived hydrochar, which could be utilized to adjust hydrochar properties for specific applications (e.g., adsorbent, fuel) by regulating respective proportions of each component in bio-waste. Cellulose, hemicellulose and lignin were used as the control variables of feedstocks composition in this work. After hydrothermal process, lignin added feedstock produced more hydrochar, which contained rougher surface with nearly doubled BET areas and more benzene rings. Hemicellulose-aided hydrochar possessed higher density of carbonaceous microspheres and richer hydroxyl. This char was simultaneously covered by more esters or lactones with more aromatic oxygen-containing groups inside. Similar to hemicellulose, cellulose improved the formation of diverse oxygenous groups but reduced the size of microspheres on hydrochar.

Further Insight into the Formation and Oxidation of CaCr2O4 during Solid Fuel Combustion

The control of toxic chromate (Cr6+) formation is still a significant challenge in solid fuel combustion. In particular, the mechanism of chromium transformation from Cr3+ to chromate or other unoxidized forms remains unclear. The present study confirms the formation of a significant unoxidized Cr-containing compound CaCr2O4(Cr3+) during solid fuel combustion. Experiments were conducted, for the first time, to clarify the mechanism of CaCr2O4 oxidation, which is quite different from Cr2O3 oxidation. The findings demonstrate that CaCr2O4 was formed at temperatures above 1200 K, through rapid decomposition of CaCrO4 or slow and direct interaction between CaO and Cr2O3. Compared to Cr2O3, CaCr2O4 could be oxidized at lower temperatures under the influence of free CaO. In the absence of free CaO, the oxidation of CaCr2O4 was minimal; however, in the presence of CaSO4, calcium in the form of CaCr2O4 participated in the oxidation of CaCr2O4. Thus, chromium in the form of CaCr2O4 was more likely to be oxidized when CaCr2O4-containing fly ash was reheated. Fortunately, CaCr2O4 showed slight basicity on the surface, allowing it to react with acidic gases. Accordingly, measures were proposed to suppress the oxidation of CaCr2O4 by stimulating the reactions between CaCr2O4 and acidic substances, like SO2 and Si/Al-compounds. These compounds competed with chromium at high temperatures to react with calcium in the fly ash and in CaCr2O4. As a result, the unoxidized chromium was transformed into highly stable Cr2O3 or Ca3Cr2 (SiO4)3.