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At least 829 records · Page 46

Tuning Sugarcane Bagasse Biochar into a Potential Carbon Black Substitute for Polyethylene Composites

One of the most used carbonaceous materials by industry are carbon blacks, which have technological applications in polymeric composites, coatings and paints, electric and electrochemical devices. One drawback is that they are produced from fossil fuels. Although biochars are also carbonaceous materials some disadvantages like their larger particles size, high ash content and highly oxygenated surface must be overcome to enable their use as substitute of carbon blacks in composites. Sugarcane bagasse biochar was used to produce carbonaceous materials to substitute carbon blacks. Milling of biochar decreased particle size from several hundreds of micrometers to 100–500 nm and narrowed its size distribution. Chemical leaching reduced the inorganic compounds and ash content by almost 20%. Great advance was achieved when biochar was thermally annealed in alcohol vapor atmosphere which resulted in biochar-based material with very low oxygenated carbon species at particles surface and turned them hydrophobic. Almost no C–O/C=O and O–C=O peaks components were observed at the X-ray photoelectron spectroscopy spectrum. Reactive thermal annealing of the biochar based additive was a key procedure to obtain polyethylene composites (5% loading) with mechanical, thermal and colorimetric properties very close to the ones prepared with the carbon black from fossil fuels.

36 MATERIALS SCIENCE↗

Reactions in the Tuyere Zone of Ironmaking Blast Furnace

A series of slags can be formed in the lower part of the ironmaking blast furnace that play important roles in smooth furnace operation, and in determining iron quality and productivity. The final slag tapped from the BF has been investigated extensively as it can be collected directly. Unfortunately, difficulties in accessing the interiors of the blast furnace limit the full understanding of other slags such as primary and bosh slags. In this study, different types of samples directly obtained from the tuyere zone of the blast furnace have been systematically analyzed and characterized using scanning electron microscopy (SEM), electron probe X-ray microanalysis (EPMA), and X-ray fluorescence (XRF), with focus on the characteristics of slags formed in the tuyere level. The samples were identified into three groups according to their morphological, mineralogical, and chemical properties: (1) tuyere slags originating from the reactions between ash and dripping slags; (2) bosh slags in the CaO-SiO{sub 2}-Al{sub 2}O{sub 3}-MgO-FeO system, with a CaO/SiO{sub 2} weight ratio of around 1.50, and Al{sub 2}O{sub 3} and MgO concentrations close to those of final slags; and (3) coke ash that did not react with bosh slags. These findings will provide useful information on the evaluation of slags inside the blast furnace and the reactions in the tuyere zone.

36 MATERIALS SCIENCE↗

Phosphonate functionalized magnetic mesoporous silica for rare earth element recovery from citrate assisted solid waste extracts

The growing high demand of rare earth elements (REEs) has prompted extensive research on REE recovery from waste streams. This study reports the synthesis and evaluation of phosphonate-functionalized magnetic mesoporous silica (MMS-PP) for REE recovery from the acidic extracts of solid wastes. MMS-PP was synthesized using surfactant template and post-synthesis methods, and tested using simulated and real extraction solutions from citrate-assisted REE extracts from municipal solid waste incineration (MSWI) ash. The organic-inorganic hybrid MMS-PP was evaluated for La recovery from 50 mM simulated citrate extract, with the adsorption capacity of 13.5 mg/g compared to ∼2.5 mg/g for non-functionalized MMS. The MMS-PP material exhibited fast adsorption within 10 min, good La selectivity against competing Na + and Ca 2+ , moderate selectivity against Al 3+ and Fe 3+ , high recyclability over multiple adsorption-desorption cycles, and equivalent efficiency for La, Ce, Nd, and Y recovery. Furthermore, the MMS-PP material also demonstrated 70–95% REE recovery from real citrate extracts of MSWI ash, and the spent MMS-PP material can be regenerated and reused for multiple cycles. Functionalized mesoporous materials in combination with organic-ligand assisted extraction can potentially provide a green, effective, and tunable solid-liquid separation platform for REE recovery from complex solid waste streams.

REE recovery↗

Discovering the feasibility of using the radiation forces for recovering rare earth elements from coal power plant by-products

The feasibility of using laser separation for rare earth recovery from coal ashes was explored. To do so, laser-induced motion and travel distances of some rare earth and rare earth oxides (Lu2O3, Yb2O3, HfO2, Dy2O3, Ta2O5, Tm, Lu, Ho, TeO2, La2O3, Ho, TiO2, Fe2O3 Y2O3, GeO2, Sc2O3) and mineral compounds (MgO, CaO, Al2O3, SiO2, KCl) that are commonly found is coal ashes were numerically investigated. The investigations were carried out for particles in quiescent air, (T = 300 K, μ = 18.46 x 10-6 N-s/m2 , ρ = 1.177 kg/m3 ) exposing to a CW laser beam of 6 mm in diameter and it was focused by a 500 mm focal length lens. The results showed that the separation distances between these elements varied from few micrometers to several millimeters and it became widened as the laser power increased. The important result presented here is that all rare earth oxides were separated and concentrated in a small area located near the beam waist while all other mineral compounds traveled further and concentrated in a small area far from the beam waist.

36 MATERIALS SCIENCE↗

Changes in feedstock quality in willow chip piles created in winter from a commercial scale harvest

Storage and handling are important facets of biomass logistics because there are associated costs and biomass properties can change significantly as material proceeds through the supply chain. Thus, this aspect of biomass supply systems requires continued study. Shrub willow chips were harvested, and used to create six piles that each contained between 10 and 22 Mg (fresh biomass). Material was monitored for several months in temporary storage to assess changes in biomass quality (moisture, ash and energy content). Internal pile temperatures increased due to biological activity and conditions within a pile quickly differentiated based on location (shell, core, top, and side). Mean moisture content increased from 42 to 47% (mass fraction) between harvest and delivery of the chips, but ranged between 37 and over 60% over the next three months depending on pile location with the shell generally drier than the core. Mean ash content increased 1 to 2% points (mass fraction) between harvesting, reloading and delivery to the trial location, but became more variable during storage. Higher heating values (HHV) were stable between 18.6 and 19.0 MJ kg –1 over the six months, but lower heating values (LHV) ranged between 8.6 and 11.7 MJ kg –1 and mirrored changes in moisture content. There was minimal change in chip quality over two months, but quality became more variable over longer time periods. In conclusion, this period could be extended, and negative effects on chip quality could be mitigated, by improving storage methods, blending different types of chips, or employing pretreatments.

09 BIOMASS FUELS↗

Chloride diffusivity, chloride threshold, and corrosion initiation in reinforced alkali-activated mortars: Role of calcium, alkali, and silicate content

The aim of this study is to investigate systematically the chloride diffusivity and chloride threshold of a wide range of calcium-rich and fly ash-dominated alkali-activated samples in light of their compositional differences. To this end, the effects of various fly ash (FA)-to-slag ratios, of alkali concentrations and of silicate content in the activator were investigated. The electrochemical aspects of the passive samples were also assessed. Results show the prominent role of calcium in the matrix to reduce the chloride diffusivity. While higher alkali concentration increased the porosity and chloride diffusivities in general, lower modulus ratios provided considerably better performance in the FA-dominated samples. Chloride threshold values range between 0.19 (wt% binder mass) for calcium-rich mortars fabricated at low levels of alkalinities and 0.69 for FA-dominated mortars fabricated with highly alkaline activators. Half-cell potential and polarization resistance of alkali-activated samples were in general lower than their Portland cement counterparts.

36 MATERIALS SCIENCE↗

Water vapor sorption isotherms, pore structure, and moisture transport characteristics of alkali-activated and Portland cement-based binders

Moisture transport plays a key role in determining the different durability-related features of cementitious materials. In this paper, moisture sorption in a range of low-calcium (geopolymer-type) and calcium-rich alkali-activated binders are studied and compared with that of Portland cement-based binders. Through the analysis of water vapor sorption isotherms (WVSI) and mercury intrusion porosimetry (MIP) test results, two vastly different pore structures were observed. Fly ash-based geopolymer-type binders showed a very porous structure where a large volume of mesopores coexisted with a significant volume of macropores. Alkali-activated slag binders, however, had a very fine pore structure, with a relative lack of large macropores. The different pore structure of fly ash-based and slag-based binders led to amplification of pore blocking and cavitation in blended systems by the addition of slag. Analysis of the sorption kinetics showed the prominent effect of the presence of calcium in the matrix to reduce the permeability.

36 MATERIALS SCIENCE↗

Assessment the leaching characteristics and long-term leaching behavior of some radionuclides from synthesized zeolite cement matrix

Highlights: • Synthesis and characterization of zeolite cement synthesized from fly ash • Leaching tests were used to assess the release rate of {sup 85}Sr and {sup 60}Co radionuclides. • Simple mathematical models were used to detect leaching mechanisms. • Long-term leaching behavior of {sup 85}Sr and {sup 60}Co from cementitious matrix was assessed. The development of cementitious materials remains a vital goal to produce valuable products with good mechanical, physical and chemical properties suitable for the safe disposal of concentrated radionuclides resulted from the treatment of contaminated solutions. In this paper, zeolite cement with good properties was laboratory synthesized from industrial by-products fly ash and characterized using various characterization techniques. The leaching characteristics of strontium and cobalt radionuclides from the synthesized zeolite cement were scrutinized conforming with the standard leaching methodology of International Atomic Energy Authority (IAEA). A mechanical strength assessment was executed to characterize the extent of immobilization process of the solidified matrices. The cumulative leaching fraction (φ) of the two studied radionuclides was found to be less than 5% in all examined conditions, which implies the applicability of the IAEA-recommended methodology for estimating the diffusion coefficient. The experimental leaching data were regressed nonlinearly to various mathematical kinetic models to assess the controlling leaching mechanism and to determine the leaching parameters. The regression results indicated that strontium ({sup 85}Sr) and cobalt ({sup 60}Co) leaching resulted from two succeeding mechanisms: as first order kinetic reaction, and then diffusion. The calculated values of leachability indices signify that the performance of each of the studied matrices is within an acceptable range. A simplified mathematical model, rooted in the first order reaction and diffusion mechanisms, was simulated to predict the radionuclides leaching rates from zeolite cement matrices. By comparing the synthesized zeolite cement with other cementitious materials, it can be concluded that the synthesized material can be classified as an efficient material suitable to immobilize {sup 85}Sr and {sup 60}Co from radioactive wastes. The acquired findings demonstrated that the studied immobilized waste matrices have acceptable mechanical effectiveness.

36 MATERIALS SCIENCE↗

Assessment of lignite upgrade and hydrogen evolution via electrolysis

Lignite, considered as the lowest-rank coal, accounts for 45% of the total coal resources worldwide, and its low carbon and high ash contents limit its large-scale application. In order to upgrade lignite effectively, a modified coal electrolytic cell (MCEC) was designed, built, and then evaluated for lignite upgrade and hydrogen production through electrolysis, and the operating conditions were optimized. The results show that the performance of the MCEC outperformed the previous coal electrolytic cell (CEC). The operating temperature and iron concentration significantly impact the average current density per milligram of catalyst (ACDMC). The content of dry fixed carbon and heating value increased by 20.9% (wt%) and 8.15%, respectively, in electrolyzed lignite compared with raw lignite. Besides, 71.5% ash and 39.6% mercury were removed from raw lignite after electrolysis, which is the first report. The Faradaic efficiency (FE) for hydrogen evolution reached 99% using MCEC. In addition, the analysis of spectroscopy methods (SEM, EDX, FTIR, and XRD) revealed that the lignite particles were cracked; the oxygen-containing functional groups increased; the minerals of quartz and hematite formed on the surface of lignite particles after electrolysis. Furthermore, the facts indicate that electrolysis of lignite is a competitive approach for lignite upgrade and hydrogen production.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Speciation, behaviour, and fate of mercury under oxy-fuel combustion conditions

The work presented here reports the first study in which the speciation, behaviour and fate of mercury (Hg) have been evaluated under oxy-fuel combustion at the largest oxy-Pulverised Coal Combustion (oxy-PCC) demonstration plant to date during routine operating conditions and partial exhaust flue gas re-circulation to the boiler. The effect of the CO{sub 2}-rich flue gas re-circulation on Hg has also been evaluated. Results reveal that oxy-PCC operational conditions play a significant role on Hg partitioning and fate because of the continuous CO{sub 2}-rich flue gas re-circulations to the boiler. Mercury escapes from the cyclone in a gaseous form as Hg{sup 2+} (68%) and it is the prevalent form in the CO{sub 2}-rich exhaust flue gas (99%) with lower proportions of Hg{sup 0} (1.3%). The overall retention rate for gaseous Hg is around 12%; Hg{sup 0} is more prone to be retained (95%) while Hg{sup 2+} shows a negative efficiency capture for the whole installation. The negative Hg{sup 2+} capture efficiencies are due to the continuous CO{sub 2}-rich exhaust flue gas recirculation to the boiler with enhanced Hg contents. Calculations revealed that 44 mg of Hg were re-circulated to the boiler as a result of 2183 re-circulations of CO{sub 2}-rich flue gas. Especial attention must be paid to the role of the CO{sub 2}-rich exhaust flue gas re-circulation to the boiler on the Hg enrichment in Fly Ashes (FAs). - Highlights: • The fate of gaseous Hg has been evaluated under oxy-fuel combustion. • The Hg oxidation process is enhanced in CO{sub 2}-rich flue gas recirculation. • Hg{sup 2+} is the prevalent gas species in the CO{sub 2}-rich exhaust flue gas. • Hg{sup 2+}{sub (g)} shows a negative efficiency capture for the whole installation. • Especial attention must be paid to the Hg enrichment in Fly Ashes.

54 ENVIRONMENTAL SCIENCES↗

Pre-combustion mercury removal with co-production of hydrogen via coal electrolysis

Here, pre-combustion mercury removal via coal electrolysis was performed and investigated on a bench-scale coal electrolytic cell (CEC) systemically, and factorial design was used to determine the effect of different operating conditions (coal particle size, operating temperature, operating cell voltage, and flow rate of slurry) on the percentage of mercury removal, percentage of ash removal, and dry heating value change. The results showed that the operating cell voltage, as well as the interaction between operating cell voltage and coal particle size, are significant factors in the percentage of mercury removal. There is no significant factor in the percentage of ash removal and the dry heating value change, but the coal could be purified while keeping the dry heating value almost constant after electrolysis. A co-product of hydrogen could be produced during coal electrolysis with 50% lower energy consumption compared with water electrolysis. Meanwhile, a mechanism for mercury removal in coal was proposed. The facts indicate that coal electrolysis is a promising method for pre-combustion mercury removal.

54 ENVIRONMENTAL SCIENCES↗

Synthesis and characterization of negative thermal expansion HfW{sub 2-x}V{sub x}O{sub 8-x/2} solid solutions

Cubic HfW{sub 2-x}V{sub x}O{sub 8-x/2} (c-HfW{sub 2-x}V{sub x}O{sub 8-x/2}) solid solutions, where x is up to 0.34, were synthesized using a process of acidic steam hydrothermal (ASH)-thermal dehydrating precursors. The process is studied detailedly. The results reveal tetragonal HfW{sub 2-x}V{sub x}O{sub 7-x/2}(OH){sub 2}(H{sub 2}O){sub 2} precursors are synthesized after ASH treatment and they produce orthorhombic HfW{sub 2-x}V{sub x}O{sub 8-x/2} in dehydrating. Then c-HfW{sub 2-x}V{sub x}O{sub 8-x/2} are obtained at higher temperature. The crystal structures of c-HfW{sub 2-x}V{sub x}O{sub 8-x/2} are characterized as {alpha}-HfW{sub 2}O{sub 8} and {beta}-HfW{sub 2}O{sub 8} structure for 0{<=}x{<=}0.30 and x=0.34, respectively. All the c-HfW{sub 2-x}V{sub x}O{sub 8-x/2} show excellent negative thermal expansion property. The relationships between the properties, such as ordered degree parameter, crystal lattice parameter, phase transition temperature and linear average thermal expansion coefficient, and the V content are also discussed. - Graphical abstract: Novel c-HfW{sub 2-x}V{sub x}O{sub 8-x/2} solid solutions were synthesized and all of them still show excellent negative thermal expansion property. Highlights: Black-Right-Pointing-Pointer Novel cubic HfW{sub 2-x}V{sub x}O{sub 8-x/2} solid solutions and their precursors were synthesized. Black-Right-Pointing-Pointer Cubic HfW{sub 2-x}V{sub x}O{sub 8-x/2} solid solutions show excellent negative thermal expansion. Black-Right-Pointing-Pointer The relationship between the properties of the samples and the V content is revealed. Black-Right-Pointing-Pointer x up to 0.34, a rare large solid solubility in aliovalent substitution.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Effect of sewage sludge content on gas quality and solid residues produced by cogasification in an updraft gasifier

Highlights: Black-Right-Pointing-Pointer Cogasification of sewage sludge with wood pellets in updraft gasifier was analysed. Black-Right-Pointing-Pointer The effects of sewage sludge content on the gasification process were examined. Black-Right-Pointing-Pointer Sewage sludge addition up to 30 wt.% reduces moderately the process performance. Black-Right-Pointing-Pointer At high sewage sludge content slagging and clinker formation occurred. Black-Right-Pointing-Pointer Solid residues produced resulted acceptable at landfills for non-hazardous waste. - Abstract: In the present work, the gasification with air of dehydrated sewage sludge (SS) with 20 wt.% moisture mixed with conventional woody biomass was investigated using a pilot fixed-bed updraft gasifier. Attention was focused on the effect of the SS content on the gasification performance and on the environmental impact of the process. The results showed that it is possible to co-gasify SS with wood pellets (WPs) in updraft fixed-bed gasification installations. However, at high content of sewage sludge the gasification process can become instable because of the very high ash content and low ash fusion temperatures of SS. At an equivalent ratio of 0.25, compared with wood pellets gasification, the addition of sewage sludge led to a reduction of gas yield in favor of an increase of condensate production with consequent cold gas efficiency decrease. Low concentrations of dioxins/furans and PAHs were measured in the gas produced by SS gasification, well below the limiting values for the exhaust gaseous emissions. NH{sub 3}, HCl and HF contents were very low because most of these compounds were retained in the wet scrubber systems. On the other hand, high H{sub 2}S levels were measured due to high sulfur content of SS. Heavy metals supplied with the feedstocks were mostly retained in gasification solid residues. The leachability tests performed according to European regulations showed that metals leachability was within the limits for landfilling inert residues. On the other hand, sulfate and chloride releases were found to comply with the limits for non-hazardous residues.

54 ENVIRONMENTAL SCIENCES↗

Towards a coherent European approach for taxation of combustible waste

Highlights: • Current European waste taxes do not constitute a level playing field. • Integrating waste incineration in EU ETS avoids regional tax competition. • A differentiated incineration tax is a second-best instrument for NO{sub x} emissions. • A tax on landfilled incineration residues stimulates ash treatment. - Abstract: Although intra-European trade of combustible waste has grown strongly in the last decade, incineration and landfill taxes remain disparate within Europe. The paper proposes a more coherent taxation approach for Europe that is based on the principle of Pigovian taxation, i.e. the internalization of environmental damage costs. The approach aims to create a level playing field between European regions while reinforcing incentives for sustainable management of combustible waste. Three important policy recommendations emerge. First, integrating waste incineration into the European Emissions Trading System for greenhouse gases (EU ETS) reduces the risk of tax competition between regions. Second, because taxation of every single air pollutant from waste incineration is cumbersome, a differentiated waste incineration tax based on NO{sub x} emissions can serve as a second-best instrument. Finally, in order to strengthen incentives for ash treatment, a landfill tax should apply for landfilled incineration residues. An example illustrates the coherence of the policy recommendations for incineration technologies with diverse environmental effects.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

Decreased PCDD/F formation when co-firing a waste fuel and biomass in a CFB boiler by addition of sulphates or municipal sewage sludge

Highlights: • Two strategies to reduce PCDD/F formation when co-firing solid recovered fuel (SRF) and biomass. • They were co-combustion with municipal sewage sludge (MSS) and addition of ammonium sulphate. • PCDD/Fs were significantly reduced for a biomass rich in chlorine when adding ammonium sulphate. • MSS had a suppressing effect on PCDD/F formation during co-combustion with SRF. • A link is presented between gaseous alkali chlorides, chlorine in deposits and PCDD/F formation. - Abstract: Polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) are formed during waste incineration and in waste-to-energy boilers. Incomplete combustion, too short residence times at low combustion temperatures (<700 °C), incineration of electronic waste and plastic waste containing chlorine are all factors influencing the formation of PCDD/Fs in boilers. The impact of chlorine and catalysing metals (such as copper and iron) in the fuel on PCDD/F formation was studied in a 12 MW{sub th} circulating fluidised bed (CFB) boiler. The PCDD/F concentrations in the raw gas after the convection pass of the boiler and in the fly ashes were compared. The fuel types were a so-called clean biomass with low content of chlorine, biomass with enhanced content of chlorine from supply of PVC, and solid recovered fuel (SRF) which is a waste fuel containing higher concentrations of both chlorine, and catalysing metals. The PCDD/F formation increased for the biomass with enhanced chlorine content and it was significantly reduced in the raw gas as well as in the fly ashes by injection of ammonium sulphate. A link, the alkali chloride track, is demonstrated between the level of alkali chlorides in the gas phase, the chlorine content in the deposits in the convection pass and finally the PCDD/F formation. The formation of PCDD/Fs was also significantly reduced during co-combustion of SRF with municipal sewage sludge (MSS) compared to when SRF was fired without MSS as additional fuel.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Tar-free fuel gas production from high temperature pyrolysis of sewage sludge

Highlights: • High temperature pyrolysis of sewage sludge was efficient for producing tar-free fuel gas. • Complete tar removal and volatile matter release were at elevated temperature of 1300 °C. • Sewage sludge was converted to residual solid with high ash content. • 72.60% of energy conversion efficiency for gas production in high temperature pyrolysis. • Investment and costing for tar cleaning were reduced. - Abstract: Pyrolysis of sewage sludge was studied in a free-fall reactor at 1000–1400 °C. The results showed that the volatile matter in the sludge could be completely released to gaseous product at 1300 °C. The high temperature was in favor of H{sub 2} and CO in the produced gas. However, the low heating value (LHV) of the gas decreased from 15.68 MJ/N m{sup 3} to 9.10 MJ/N m{sup 3} with temperature increasing from 1000 °C to 1400 °C. The obtained residual solid was characterized by high ash content. The energy balance indicated that the most heating value in the sludge was in the gaseous product.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Lab-scale pyrolysis of the Automotive Shredder Residue light fraction and characterization of tar and solid products

Highlights: • Car fluff was pyrolysed at various temperatures. • Condensable gases (tar) and solid residue obtained were characterized. • Char had low HHV, high metal content and low PAH concentration. • Tar had high HHV and can be used as an alternative fuel. • Toxicity of tar changes with temperature, the greatest contribution is from PCDFs. - Abstract: The general aim of this study is the recovery of Automotive Shredder Residue (ASR). The ASR light fraction, or car fluff, that was collected at an Italian shredding plant was pyrolysed at various temperatures (500–800 °C) in a lab-scale reactor. The condensable gases (tar) and solid residue yields increased with decreasing temperature, and these products were characterized to suggest a potential use to reclaim them. The higher heating value (HHV) of tar was 34–37 MJ/kg, which is comparable with those of fossil fuels. Furthermore, the ash content was low (0.06–4.98%). Thus, tar can be used as an alternative fuel. With this prospect, the concentrations of polychlorinated dibenzodioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) in tar were determined. The toxicity of tar changes with temperature (1–5 ng I-TEQ/g), and the PCDFs significantly contribute to tar toxicity, which was 75–100% with a maximum of 99.6% at 700 °C. Regarding the characterization of the solid residue, the low HHV (2.4–3.3 MJ/kg) does not make it suitable for energy recovery. Regarding material recovery, we considered its use as a filler in construction materials or a secondary source for metals. It shows a high metal concentration (280,000–395,000 mg/kg), which is similar at different pyrolysis temperatures. At 500 °C, polycyclic aromatic hydrocarbons (PAHs) were not detected in the solid residue, whereas the maximum total PAH concentration (19.41 ng/g, 700 °C) was lower than that in fly ash from MSWI. In conclusion, 500 °C is a suitable pyrolysis temperature to obtain valuable tar and solid residue.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

Optimization and characterization of hydrochar produced from microwave hydrothermal carbonization of fish waste

Highlights: • Microwave hydrothermal carbonization (MHTC) converts fish waste to hydrochar. • MHTC of fish waste at ∼200 °C for ∼119 min produces maximal hydrochar yield (∼34%). • Based on MHTC conditions, hydrochar has ∼25–57% atomic carbon, and ∼20–28% ash. • Microsphere-rich hydrochar has energy value that ranges from 19 to 24.5 MJ/kg. • MHTC can convert pure non-lignocellulosic fish waste to good quality hydrochar. - Abstract: Fish processing results in large amounts of solid and liquid wastes that are unsustainably dumped into oceans and landfills. Alternative sustainable technologies that completely utilize seafood wastes are needed. Hydrothermal carbonization (HTC) that converts moisture-rich biomass into hydrochar is mostly employed for pure lignocellulosic biowaste. However, the suitability of HTC for pure non-lignocellulosic waste is unknown. Here, for the first time, a response surface design guided optimization of microwave hydrothermal carbonization (MHTC) process parameters, holding temperature (150–210 °C) and time (90–120 min), showed that a temperature of approximately 200 °C and a time of approximately 119 min yielded maximal hydrochar (∼34%). The atomic carbon and ash content, and calorific value of hydrochar were approximately 25–57%, 20–28%, and 19–24.5 MJ/kg respectively, depending on the MHTC operating conditions. Taken together, these results confirm that MHTC produces hydrochar from fish waste of quality comparable to one produced from certain lignocellulosic, sewage and municipal wastes. Therefore, this strategy presents an exciting alternative technology that can be used either independently or in combination with other valorization techniques to completely utilize fish wastes irrespective of their quality.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗