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This study investigated the characteristics of banana peel biochar (BPB) produced from two particle sizes of banana waste at varying temperatures. The biochar yield decreased with increasing temperature and decreasing particle size. Physicochemical analysis showed the presence of amorphous carbon, fullerene, and chaolite in BPB produced at 500 °C. X-ray fluorescence(XRF) analysis showed high carbon, potassium, and chlorine percentages in BPB. BPB was found to be a promising adsorbent for copper (Cu2+) removal, with a maximum adsorption capacity of 54.9 mg/g and optimal Cu2+ concentrations for adsorption at 450 and 550 mg/L.

The present review deals with water applications in sub and supercritical conditions with a focus on supercritical water oxidation process (SCWO) as an example of high temperature and pressure technologies. It starts by presenting the advantages of water properties near and beyond the critical point and the major applications exploiting them. Then, it presents a review on SCWO from the description of the process, the reaction mechanism and kinetics to reactor design and modeling. It also presents the main problems and difficulties that delay the SCWO industrial application, and summarizes the main efforts and research to overcome them for a safe, efficient and economic process.

The transition from the use of fossil fuels to renewable and green energy is a worldwide challenge that must be seriously considered in order to ensure sustainable development and the preservation of the environment. The conversion of wet biomasses (i.e., sewage sludge) into energy through thermochemical processes in general and hydrothermal carbonization (HTC) in particular has been pointed out as an interesting and attractive approach for the energetic and agricultural valorization of the produced solid residues, named hydrochars. The success of such valorization options is highly dependent on these hydrochars’ physico-chemical and energetic properties that are influenced not only by the type of the sludge (urban or industrial) and its nature (primary, secondary, or digested) but also by the HTC parameters, especially temperature, pressure, and residence time. This editorial provides a summary of the latest studies regarding the impact of the cited above parameters on the properties of the produced hydrochars. The economic and environmental feasibility of this process for sewage sludge management is also presented.

The demand for clean energy is strongly related with many European and other global legislations and directives [...]

This paper presents an in-depth characterization of a raw industrial sludge (IS-R) and its KOH-activated biochar pyrolyzed at 750 °C (IS-KOH-B) followed by their application to remove a cationic dye from aqueous solution. Materials characterization shows that compared to the IS-R, the IS-KOH-B has improved structural, textural, and surface chemical properties. In particular, the IS-KOH-B’s BET surface area and total pore volume are about 78 and 6 times higher than those found for the IS-R, respectively. The activated biochar efficiently retained the cationic dye under wide experimental conditions. Indeed, for an initial dye concentration of 50 mg L−1, removal yields were assessed to be more than 92.5%, 93.5%, and 97.8% for a large pH range (4–10), in the presence of high contents of competing cations (3000 mg L−1 of Ca2+, Mg2+, Na+, and K+), and a low used adsorbent dose (1 g L−1), respectively. The Langmuir’s adsorption capacities were 48.5 and 65.9 mg g−1 for of IS-R and IS-KOH-B, respectively, which are higher than those reported for various adsorbents in the literature. The dye removal was found to be monolayer, spontaneous, and endothermic for both the adsorbents. Moreover, this removal process seems to be controlled by chemical reactions for IS-KOH-B whereas by both physico–chemical reactions for IS-R. This study demonstrates that the raw industrial sludge and especially its KOH-activated derived biochar could be considered as promising adsorbents for the removal of dyes from aqueous solutions.

This work examines in silico the dominant geochemical processes that control inorganic nutrients (Ca, Mg, Na, K) availability in irrigated agricultural soil amended with potassium-enriched biochar (from olive mill wastes) at mass doses of 0.5%, 1%, 2% and 10%. The geochemical modelling step was supported by analytical measurements regarding the physicochemical characteristics of the irrigation water, the agricultural soil and the biochar. Two geochemical approaches, namely equilibrium exchange (E.E.) and kinetic exchange (K.E.) models were applied and compared to assess nutrient release with an emphasis on potassium availability. Equilibrium exchange perspective assumed that nutrient release is controlled by ion-exchange reactions onto the biochar surface, whilst kinetic exchange perspective assumed the contribution of both ion-exchange and dissolution of salts. Results indicated that for the E.E. model, the soluble amount of potassium is readily available for transport within the pores of the porous media, and therefore is leached from the column within only 10 days. For the K.E. model that assumes a kinetically controlled release of potassium due to interactions occurring at the solid-solution interface, the assessed retention times were more realistic and significantly higher (up to 100 days). Concerning the applied doses of biochar, for a 2% biochar fraction mixed with soil, for example, the available K for plants doubled compared with the available K in the soil without biochar. In any case, the use of numerical modeling was proven helpful for a quick assessment of biochar performance in soil, by avoiding time-consuming and laborious experimental set-ups. Validation of the models by experimental data will further establish the proposed mechanisms.

Terrorism is a crucial danger to the world, especially the Middle East. As Jordan is amidst countries with armed conflicts, its natural resources (in particularly, water resources) are vulnerable to terrorist attacks. In this paper, possible biological and chemical weapons that can be used as intimidation, along with their threats, vulnerabilities, and inactivation methods, concerning water treatment processes in the municipality of Irbid, are studied. Irbid is the second largest city in terms of population in Jordan, after the capital city of Amman, and it is the nearest governorate to Syria borders that is considered a war zone. After conducting risk assessment that takes into consideration criticality, threats, and vulnerability, it appears that only one of the eight units, which is the Makhraba pumping station, along with the Bushra water tank, were identified as medium risk. The other units have treatment processes and proper precautions that are able to inactivate or prevent any possible contamination. A response plan should be set by developing a telemetry system with specific sensors that can detect any sudden and unacceptable threats to the water quality and that has the ability to shut down the concerned units automatically.

Since buildings are one of the major contributors to global warming, efforts should be intensified to make them more energy-efficient, particularly existing buildings. This research intends to analyze the energy savings from a suggested retrofitting program using energy simulation for typical existing residential buildings. For the assessment of the energy retrofitting program using computer simulation, the most commonly utilized residential building types were selected. The energy consumption of those selected residential buildings was assessed, and a baseline for evaluating energy retrofitting was established. Three levels of retrofitting programs were implemented. These levels were ordered by cost, with the first level being the least costly and the third level is the most expensive. The simulation models were created for two different types of buildings in three different climatic zones in Palestine. The findings suggest that water heating, space heating, space cooling, and electric lighting are the highest energy consumers in ordinary houses. Level one measures resulted in a 19–24 percent decrease in energy consumption due to reduced heating and cooling loads. The use of a combination of levels one and two resulted in a decrease of energy consumption for heating, cooling, and lighting by 50–57%. The use of the three levels resulted in a decrease of 71–80% in total energy usage for heating, cooling, lighting, water heating, and air conditioning.

This Special Issue includes investigations related to wastewater treatment, recovery, and reuse [...]

Lignite, as an available and low-cost material, was tested for cadmium (Cd) and copper (Cu) removal from aqueous solutions under various static experimental conditions. Experimental results showed that the removal efficiency of both metals was improved by increasing their initial concentrations, adsorbent dosage and aqueous pH values. The adsorption kinetic was very rapid for Cd since about 78% of the totally adsorbed amounts were removed after a contact time of only 1 min. For Cd and Cu, the kinetic and isothermal data were well fitted with pseudo-second order and Freundlich models, respectively, which suggests that Cd/Cu removal by lignite occurs heterogeneously on multilayers surfaces. The maximum Langmuir’s adsorption capacities of Cd and Cu were assessed to 38.0 and 21.4 mg g−1 and are relatively important compared to some other lignites and raw natural materials. Results of proximate, scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDS), Fourier transform infrared spectroscopy (FTIR) and X-Ray diffraction (XRD) showed that the removal of these metals occurs most likely through a combination of cation exchange and complexation with specific functional groups. The relatively high adsorption capacity of the used lignite promotes its future use as a low cost material for Cd and Cu removal from effluents, and possibly for other heavy metals or groups of pollutants.

This paper aims at investigating the production of high quality briquettes from olive mill solid waste (OMSW) mixed with corn starch as a binder for energy production. For this purpose, different mass percentages of OMSW and binder were considered; 100%-0%, 90%-10%, 85%-15%, and 70%-30%, respectively. The briquetting process of the raw mixtures was carried out based on high pressures. Physico-chemical and mechanical characterizations were performed in order to select the best conditions for the briquettes production. It was observed that during the densification process, the optimal applied pressure increases notably the unit density, the bulk density, and the compressive strength. Mechanical characterization shows that the prepared sample with 15% of corn starch shows the best mechanical properties. Moreover, the corn starch binder affects quietly the high heating value (HHV) which increases from 16.36 MJ/Kg for the 100%-0% sample to 16.92 MJ/Kg for the 85%-15% sample. In addition, the kinetic study shows that the binder agent does not affect negatively the thermal degradation of the briquettes. Finally, the briquettes characterization shows that the studied samples with particles size less than 100 μm and blended with 15% of corn starch binder are promising biofuels either for household or industrial plants use.

Raw poultry manure (RPM) and its derived biochars at temperatures of 400 (B400) and 600 °C (B600) were physico-chemically characterized, and their ability to release nutrients was assessed under static conditions. The experimental results showed that RPM pyrolysis operation significantly affects its morphology, surface charges, and area, as well as its functional groups contents, which in turn influences its nutrient release ability. The batch experiments indicated that nutrient release from the RPM as well as biochars attains a pseudo-equilibrium state after a contact time of about 48 h. RPM pyrolysis increased phosphorus stability in residual biochars and, in contrast, transformed potassium to a more leachable form. For instance, at this contact time, P- and K-released amounts passed from 5.1 and 25.6 mg g−1 for RPM to only 3.8 and more than 43.3 mg g−1 for B400, respectively. On the other hand, six successive leaching batch experiments with a duration of 48 h each showed that P and K release from the produced biochars was a very slow process since negligible amounts continued to be released even after a total duration of 12 days. All these results suggest that RPM-derived biochars have specific physico-chemical characteristics allowing them to be used in agriculture as low-cost and slow-release fertilizers.

Transition metal hexacyanoferrate/microporous activated carbon composites were obtained using a simple successive impregnation approach. The effect of metal type (nickel, indium, or copper), and the carbon oxidation on the composite characteristics (porosity, metal structure, and particle size), as well as on the removal efficiency of cesium from aqueous solution was investigated. Successful formation of the desired metal hexacyanoferrate phase was achieved and the size of the metallic nanoparticles and their dispersion in the carbon network was found to depend on the metal type, with the indium and nickel-based materials exhibiting the smallest particle size distribution (< 10 nm). Adsorption tests performed under batch conditions demonstrate that the copper hexacyanoferrate/activated carbon composite present the highest cesium removal capacity from aqueous solution (74.7 mg·g−1) among the three studied metal-based nanocomposites. The carbon oxidation treatment leads to the increase in the number of functional groups to the detriment of the porosity but allows for an improvement in the Cs adsorption capacity. This indicates that the Cs adsorption process is governed by the carbon surface chemistry and not its porosity. Moreover, combining oxidized carbon support with copper hexacyanoferrate induces the highest cesium adsorption capacity (101.5 mg·g−1). This could be related to synergistic effects through two absorption mechanisms, i.e., a cation exchange mechanism of Cs with the metallic hexacyanoferrate phase and Cs adsorption via carbon oxygen surface groups, as demonstrated using X-ray photoelectron spectroscopy (XPS) analyses.

Water shortage is a very concerning issue in the Mediterranean region, menacing the viability of the agriculture sector and in some countries, population wellbeing. At the same time, liquid effluent volumes generated from agro-food industries in general and olive oil industry in particular, are quite huge. Thus, the main aim of this work is to suggest a sustainable solution for the management of olive mill wastewaters (OMWW) with possible reuse in irrigation. This work is a part of a series of papers valorizing all the outputs of a three-phase system of oil mills. It deals with recovery, by condensation, of water from both OMWW and OMWW-impregnated biomasses (sawdust and wood chips), during a convective drying operation (air velocity: 1 m/s and air temperature: 50 °C). The experimental results showed that the water yield recovery reaches about 95%. The condensate waters have low electrical conductivity and salinities but also acidic pH values and slightly high chemical oxygen demand (COD) values. However, they could be returned suitable for reuse in agriculture after additional low-cost treatment.

This paper is part of a sustainable development approach, the aim being to develop a thermochemical energy recovery path while reducing the amount of tomato waste issued from agro-industrial units. The thermal process may contribute to an environmentally friendly management and help tomato processing industries creating new economic profitable circuits in an increasingly competitive context. The adopted approach was to follow the operating conditions needed for a complete thermal degradation through a thermal and kinetic analyses. The results of the tomato waste characterization confirmed their suitability to a thermochemical processing with high volatiles and fixed carbon and interesting high heating values comparable to sawdust biomass. We were able to isolate of the decomposition domains and extract kinetic parameters. Three kinetic models were applied; Flynn⁻Wall⁻Ozawa (FWO) simulated the best the combustion process. Calculated curves were validated by the first order (n = 1) model except for the slow heating rate of 5 °C/min which was fitted by the contracted cylinder model. The conclusions of this paper could help in optimizing the combustion process in order to achieve high energy recovery from tomato residues. Obtained kinetic data would help in the design of combustion reactors.

Natural gas reserves have been recently found offshore of Cyprus. Hence, a new energy sector is under development, creating potential for raised welfare for the small insular EU member. Several social and economic benefits could be achieved from the resources’ exploitation. However, natural gas is a non-renewable energy source, connected with the major environmental issues of fossil fuels. The research goal of this work was to evaluate the sustainability of the new hydrocarbons sector. This was attained using a set of indicators, developed from the combination of PESTEL (Political, Economic, Technical, Social, Environmental, Legal) and SWOT (Strengths, Weaknesses, Opportunities, Threats) analyses. These were quantified using the Analytical Hierarchy Process (AHP) weighting method. They were pairwise compared and evaluated, resulting to a size for each one. The judgements of four evaluators, representing diverse interested parties, were used. The strengths and opportunities of the sector were found to be more than the weaknesses and threats. The relevant indicators quantification demonstrates also that the value of the positives is higher than the negatives. Therefore, if the first are enhanced and the latter are mitigated, there is sustainability potential. The sectors environmental issues are evaluated as the most important, followed by the economic. The other takes lower but comparatively significant values, and must be handled accordingly. These results lead to useful conclusions and could be exploited for decision-making and policies formulation.

The present paper aims to develop a low cost, efficient, and environmentally-friendly process to purify (industrial) waters contaminated by copper by the use of oil mill wastes, through kinetic, thermodynamic, and equilibrium investigations. To do so, the raw adsorbent was characterized using different analytical techniques including X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy. Then, the interaction between copper and olive residues were examined during batch adsorption tests at various operating parameters, such as pH, initial concentration, contact time, and particle size. Kinetic data were best fitted with Broeurs-Sotolongo kinetic model. Additionally, it was found that film and intraparticle diffusion steps controlled simultaneously the mass transfer of copper onto olive mill solid waste. Among the eight tested models, Broeurs-Sotolongo isotherm suited the most the sorption, with regards to the function errors analysis. It was deduced that the adsorption of copper does not involve chemical bonds with high energy which allows easier regeneration steps and higher number of biosorbent regeneration cycles without any need for applying high temperature in the desorption reaction systems. The adsorption capacity (18.93 mg/g) calculated on the basis of this model was close to the experimental value (18.4 mg/g) but more interestingly it brought up that 50% of the generated amounts of olive wastes in Tunisia could eliminate 1.84 kTons of copper from industrial waters.

This Special Issue of Energies contains the successful invited submissions [...]

The aim of the present work is to study the effect of different activation methods for the production of a biomass-based activated carbon on the CO 2 and CH 4 adsorption. The influence of the activation method on the adsorption uptake was studied using three activated carbons obtained by different activation methods (H 3 PO 4 chemical activation and H 2 O and CO 2 physical activation) of olive stones. Methane and carbon dioxide pure gas adsorption experiments were carried out at two working temperatures (303.15 and 323.15 K). The influence of the activation method on the adsorption uptake was studied in terms of both textural properties and surface chemistry. For the three adsorbents, the CO 2 adsorption was more important than that of CH 4 . The chemically-activated carbon presented a higher specific surface area and micropore volume, which led to a higher adsorption capacity of both CO 2 and CH 4 . For methane adsorption, the presence of mesopores facilitated the diffusion of the gas molecules into the micropores. In the case of carbon dioxide adsorption, the presence of more oxygen groups on the water vapor-activated carbon enhanced its adsorption capacity.

A study was conducted to investigate the parameter that has influence on steam gasification kinetics between the biomass type and char preparation. Thermogravimetric analysis (TGA) was carried out on steam gasification of seven biomass samples as well as chars from three of these samples. Chars were prepared using three different sets of low heating rate (LHR) pyrolysis conditions including temperature and biomass bed geometry. It was shown by a characteristic time analysis that these pyrolysis conditions were not associated with a chemical regime in a large amount of devices. However, it has been shown experimentally that conditions used to prepare the char had a much lower influence on steam gasification kinetics than the biomass type.

The textural properties and surface chemistry of different activated carbons, prepared by the chemical activation of olive stones, have been investigated in order to gain insight on the NO2 adsorption mechanism. The parent chemical activated carbon was prepared by the impregnation of olive stones in phosphoric acid followed by thermal carbonization. Then, the textural properties and surface chemistry were modified by chemical treatments including nitric acid, sodium hydroxide and/or a thermal treatment at 900 °C. The main properties of the parent and modified activated carbons were analyzed by N2-adsorption, scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR) techniques, in order to enlighten the modifications issued from the chemical and thermal treatments. The NO2 adsorption capacities of the different activated carbons were measured in fixed bed experiments under 500 ppmv NO2 concentrations at room temperature. Temperature programmed desorption (TPD) was applied after adsorption tests in order to quantify the amount of the physisorbed and chemisorbed NO2. The obtained results showed that the development of microporosity, the presence of oxygen-free sites, and the presence of basic surface groups are key factors for the efficient adsorption of NO2.

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Phenolic resin and waste cotton fiber were investigated as green precursors for the successful synthesis using a soft template approach of a composite carbon with carbon nanofibers embedded in a porous carbon network with ordered and periodically pore structure. The optimal composite carbon (PhR/NC-1), exhibited a specific surface area of 394 m2∙g−1 with the existence of both microporosity and mesoporosity. PhR/NC-1 carbon was evaluated as an adsorbent of Alizarin Red S (ARS) dye in batch solution. Various operating conditions were examined and the maximum adsorption capacity of 104 mg∙g−1 was achieved under the following conditions, i.e., T = 25 °C, pH = 3, contact time = 1440 min. The adsorption and desorption heat was assessed by flow micro-calorimetry (FMC), and the presence of both exothermic and endothermic peaks with different intensity was evidenced, meaning a partially reversible nature of ARS adsorption. A pseudo-second-order model proved to be the most suitable kinetic model to describe the ARS adsorption according to the linear regression factor. In addition, the best isotherm equilibrium has been achieved with a Freundlich model. The results show that the eco-friendly composite carbon derived from green phenolic resin mixed with waste cotton fibers improves the removal of ARS dye from textile effluents.

Olive Mill Wastewater (OMWW) treatment is considered to be one of the main challenges that Mediterranean countries face. Although several procedures and technologies are mentioned in the literature, these techniques have several disadvantages or have been limited to laboratory pilot validation without posterior industrial projection. Recently, an advanced environmental friendly strategy for the recovery of OMWW was established involving the impregnation of OMWW on dry biomasses, drying of these impregnated samples, and finally green fuels and biochar production. This established strategy revealed that the drying step is crucial for the success of the entire recovery process. Hence, two impregnated samples were prepared through OMWW impregnation on sawdust (IS) and olive mill solid waste (ISW). The drying kinetics of OMWW and impregnated samples (IS and ISW) were examined in a convective dryer (air velocity range from 0.7–1.3 m/s and the temperature from 40–60 °C). The experimental results indicated that the drying of the impregnated samples occurred twice as fast as for the OMWW sample. Such behavior was attributed to the remaining thin layer of oil on the OMWW surface Furthermore, the Henderson and Pabis model showed the suitable fit of the drying curves with a determination coefficient R2 above 0.97. The drying rates were extracted from the mathematical models and the drying process was analyzed. The coefficient of effective diffusivity varied between 2.8 and 11.7 × 10−10 m2/s. In addition, the activation energy values ranged between 28.7 and 44.9 kJ/mol. These values were in the same range as those obtained during the drying of other agrifood byproducts. The final results could be very helpful to engineers aiming to improve and optimize the OMWW drying process.

The treatment of NOx from automotive gas exhaust has been widely studied, however the presence of low concentrations of NOx in confined areas is still under investigation. As an example, the concentration of NO2 can approximate 0.15 ppmv inside vehicles when people are driving on highways. This interior pollution becomes an environmental problem and a health problem. In the present work, the abatement of NO2 immission is studied at room temperature. Three activated carbons (ACs) prepared by physical (CO2 or H2O) or chemical activation (H3PO4) are tested as adsorbents. The novelty of this work consists in studying the adsorption of NO2 at low concentrations that approach real life immission concentrations and is experimentally realizable. The ACs present different structural and textural properties as well as functional surface groups, which induce different affinities with NO2. The AC prepared using water vapor activation presents the best adsorption capacity, which may originate from a more basic surface. The presence of a mesoporosity may also influence the diffusion of NO2 inside the carbon matrix. The high reduction activity of the AC prepared from H3PO4 activation is explained by the important concentration of acidic groups on its surface.

Solid char is a product of biomass pyrolysis. It contains a high proportion of carbon, and lower contents of H, O and minerals. This char can have different valorization pathways such as combustion for heat and power, gasification for Syngas production, activation for adsorption applications, or use as a soil amendment. The optimal recovery pathway of the char depends highly on its physical and chemical characteristics. In this study, different chars were prepared from beech wood particles under various pyrolysis operating conditions in an entrained flow reactor (500–1400 °C). Their structural, morphological, surface chemistry properties, as well as their chemical compositions, were determined using different analytical techniques, including elementary analysis, Scanning Electronic Microscopy (SEM) coupled with an energy dispersive X-ray spectrometer (EDX), Fourier Transform Infra-Red spectroscopy (FTIR), and Raman Spectroscopy. The biomass char reactivity was evaluated in air using thermogravimetric analysis (TGA). The yield, chemical composition, surface chemistry, structure, morphology and reactivity of the chars were highly affected by the pyrolysis temperature. In addition, some of these properties related to the char structure and chemical composition were found to be correlated to the char reactivity.