Waste to Carbon: Influence of Structural Modification on VOC Emission Kinetics from Stored Carbonized Refuse-Derived Fuel

The torrefaction of municipal solid waste is one of the solutions related to the Waste to Carbon concept, where high-quality fuel—carbonized refuse-derived fuel (CRDF)—is produced. An identified potential problem is the emission of volatile organic compounds (VOCs) during CRDF storage. Kinetic emission parameters have not yet been determined. It was also shown that CRDF can be pelletized for energy densification and reduced volume during storage and transportation. Thus, our working hypothesis was that structural modification (via pelletization) might mitigate VOC emissions and influence emission kinetics during CRDF storage. Two scenarios of CRDF structural modification on VOC emission kinetics were tested, (i) pelletization and (ii) pelletization with 10% binder addition and compared to ground (loose) CRDF (control). VOC emissions from simulated sealed CRDF storage were measured with headspace solid-phase microextraction and gas chromatography–mass spectrometry. It was found that total VOC emissions from stored CRDF follow the first-order kinetic model for both ground and pelletized material, while individual VOC emissions may deviate from this model. Pelletization significantly decreased (63%~86%) the maximum total VOC emission potential from stored CDRF. Research on improved sustainable CRDF storage is warranted. This could involve VOC emission mechanisms and environmental-risk management

The Jerusalem Balsam–a case study of a 150-year-old sample

The Jerusalem Balsam (JB) was formulated in the pharmacy of the Saint Savior monastery in the old city of Jerusalem in 1719. According to traditional sources, JB was based on an ethanolic extract of an herbal mixture. Several variations of the formulation could be found in European Pharmacopoeias, mostly recommended as an antiseptic product [1]. During the current study, an original sample of JB prepared approximately in the year 1870, as well as four contemporary samples of different variations in composition, were analyzed by gas chromatography coupled with mass spectrometry with the aid of solid phase microextraction, as well as by the liquid injection approach. About sixty different compounds have been identified in the materials–mostly essential-oil constituents. Additionally, the LC-MS and NMR (1H, HSQC, and TOCSY) profiles have been measured for the analyzed samples. Several fingerprint compounds, specific for the herbal material were found in this way. Furthermore, JB samples were tested for cytotoxicity. Two normal (J774E.1 and NIH/3T3) and two cancer cell lines (CLBL-1 [2] and CLBL70 [3]) were used in this experiment. All tested JB samples showed no cytotoxic or were very slightly toxic to normal cell lines. Only one JB sample, the almost 150-year-old one, showed a strong cytotoxic activity but only towards cancer cell lines, with the efficiency of 80-90%

The Proof-of-Concept: The Transformation of Naphthalene and Its Derivatives into Decalin and Its Derivatives during Thermochemical Processing of Sewage Sludge

One solution for sewage sludge (SS) management is thermochemical treatment due to torrefaction and pyrolysis with biochar production. SS biochar may contain toxic volatile organic compounds (VOCs) and polyaromatic hydrocarbons (PAHs). This study aimed to determine the process temperature’s influence on the qualitative PAHs emission from SS-biochar and the transformation of PAHs contained in SS. SS was torrefied/pyrolyzed under temperatures 200–600 °C with 1 h residence time. The headspace solid-phase microextraction (SPME) combined with gas chromatography and mass spectrometry (HS-SPME-GC-MS) analytical procedure of VOCs and PAHs emission was applied. The highest abundance of numerous VOCs was found for torrefaction ranges of temperature. The increase of temperatures to the pyrolytic range decreased the presence of VOCs and PAHs in biochar. The most common VOCs emitted from thermally processed SS were acetone, 2-methylfuran, 2-butanone, 3-metylbutanal, benzene, decalin, and acetic acid. The naphthalene present in SS converted to decalin (and other decalin derivatives), which may lead to SS biochar being considered hazardous material

Correction: Łyczko, J. et al. HS-SPME Analysis of True Lavender (Lavandula angustifolia Mill.) Leaves Treated by Various Drying Methods. Molecules 2019, 24, 764

The author wishes to make the following corrections to this paper [...

The Proof-of-Concept: The Transformation of Naphthalene and Its Derivatives into Decalin and Its Derivatives during Thermochemical Processing of Sewage Sludge

One solution for sewage sludge (SS) management is thermochemical treatment due to torrefaction and pyrolysis with biochar production. SS biochar may contain toxic volatile organic compounds (VOCs) and polyaromatic hydrocarbons (PAHs). This study aimed to determine the process temperature’s influence on the qualitative PAHs emission from SS-biochar and the transformation of PAHs contained in SS. SS was torrefied/pyrolyzed under temperatures 200–600 °C with 1 h residence time. The headspace solid-phase microextraction (SPME) combined with gas chromatography and mass spectrometry (HS-SPME-GC-MS) analytical procedure of VOCs and PAHs emission was applied. The highest abundance of numerous VOCs was found for torrefaction ranges of temperature. The increase of temperatures to the pyrolytic range decreased the presence of VOCs and PAHs in biochar. The most common VOCs emitted from thermally processed SS were acetone, 2-methylfuran, 2-butanone, 3-metylbutanal, benzene, decalin, and acetic acid. The naphthalene present in SS converted to decalin (and other decalin derivatives), which may lead to SS biochar being considered hazardous material.This article is published as Łyczko, Jacek, Jacek A. Koziel, Chumki Banik, and Andrzej Białowiec. "The Proof-of-Concept: The Transformation of Naphthalene and Its Derivatives into Decalin and Its Derivatives during Thermochemical Processing of Sewage Sludge." Energies 14, no. 20 (2021): 6479. DOI: 10.3390/en14206479. Copyright 2021 by the authors. Attribution 4.0 International (CC BY 4.0). Posted with permission

Effect of Filtrated Osmotic Solution Based on Concentrated Chokeberry Juice and Mint Extract on the Drying Kinetics, Energy Consumption and Physicochemical Properties of Dried Apples

Background: Filtration of osmotic solution affects selective penetration during osmotic dehydration (OD), and after drying is finished, this can influence the chemical composition of the material, which is also modified by OD. Methods: Osmotic dehydration was carried out in filtrated and non-filtrated concentrated chokeberry juice with the addition of mint infusion. Then, this underwent convective drying, vacuum-microwave drying and combined convective pre-drying, followed by vacuum-microwave finishing drying. Drying kinetics were presented and mathematical models were selected. The specific energy consumption for each drying method was calculated and the energy efficiency was determined. Results and Discussion: The study revealed that filtration of osmotic solution did not have significant effect on drying kinetics; however, it affected selective penetration during OD. The highest specific energy consumption was obtained for the samples treated by convective drying (CD) (around 170 kJ·g−1 fresh weight (fw)) and the lowest for the samples treated by vacuum-microwave drying (VMD) (around 30 kJ·g−1 fw), which is due to the differences in the time of drying and when these methods are applied. Conclusions: Filtration of the osmotic solution can be used to obtain the desired material after drying and the VMD method is the most appropriate considering both phenolic acid content and the energy aspect of drying

Enantioselective Lactonization of 3,3,6-Trimethyl-4(E)-heptenoic Acid Esters

Studies on the use of lactonization in the asymmetric synthesis of 6,6-dimethyl-4-isopropyl-3-oxabicyclo[3.1.0]hexan-2-one were described. An asymmetrically induced lactonization reaction was performed on 3,3,6-trimethyl-4(E)-heptenoic acid esters (1) and enantiomerically pure alcohols such as (−)-menthol (a), (+)-menthol (b), (−)-borneol (c), (+)-isomenthol (d), (−)-isopinocampheol (e), and (S)-(−)-1-(2-bornylphenyl)-1-ethanol (f). The enantiomerically pure alcohols that were used as ancillary chiral substances were characterized by markedly different values of induction power; menthol (a, b), borneol (c), and phenetyl alcohol (f) performed better in asymmetric δ-lactonization, whereas isomenthol (d) and isopinocampheol (e) tended to favor asymmetric γ-lactonization

The Proof-of-the-Concept of Application of Pelletization for Mitigation of Volatile Organic Compounds Emissions from Carbonized Refuse-Derived Fuel

Waste can be effectively reused through the production of carbonized refuse-derived fuel (CRDF) that enables further energy recovery. Developing cleaner production of CRDF requires consideration of practical issues of storage and handling. Thus, it needs to be ensured that CRDF does not pose an excessive risk to humans and the ecosystem. Very few studies indicate a wide variety of volatile organic compounds (VOCs) are present in CRDF, some of which are toxic. During handling, storage, transportation, and use of VOC-rich CRDF, workers and end-users could be exposed to emissions that could pose a health and safety hazard. Our recent study shows that CRDF densification via pelletization can increase the efficiency of storage and transportation. Thus, the following research question was identified: can pelletization mitigate VOCs emissions from CRDF during storage? Preliminary research aiming at the determination of the influence of CRDF pelletization on VOCs emission during storage was completed to address this question. The VOCs emissions from two types of CRDF: ground (loose, torrefied refuse-derived fuel (RDF)) and pelletized, were measured. Pelletization reduced the VOCs emissions potential during the four-day storage by ~86%, in comparison with ground CRDF. Mitigation of VOCs emissions from densified CRDF is feasible, and research is warranted to understand the influence of structural modification on VOCs emission kinetics, and possibilities of scaling up this solution into the practice of cleaner storage and transportation of CRDF