Hydrothermal carbonization (HTC) is a useful method to convert wet biomass to value-added products. Fruit waste generated in juice industries is a huge source of moist feedstock for such conversion to produce hydrochar. This paper deals with four types of fruit wastes as feedstocks for HTC; namely, rotten apple (RA), apple chip pomace (ACP), apple juice pomace (AJP), and grape pomace (GP). The operating conditions for HTC processing were 190 °C, 225 °C, and 260 °C for 15 min. For all samples, higher heating value and fixed carbon increased, while volatile matter and oxygen content decreased after HTC. Except for ACP, the ash content of all samples increased after 225 °C. For RA, AJP, and GP, the possible explanation for increased ash content above 225 °C is that the hydrochar increases in porosity after 230 °C. It was observed that an increase in HTC temperature resulted in an increase in the mass yield for RA and GP, which is in contrast with increasing HTC temperature for lignocellul... [more]

This article presents gas hydrate experimental measurements for mixtures containing methane (CH₄), carbon dioxide (CO₂) and nitrogen (N₂) with the aim to better understand the impact of water (H₂O) on the phase equilibrium. Some of these phase equilibrium experiments were carried out with a very high water-to-gas ratio that shifts the gas hydrate dissociation points to higher pressures. This is due to the significantly different solubilities of the different guest molecules in liquid H₂O. A second experiment focused on CH₄-CO₂ exchange between the hydrate and the vapor phases at moderate pressures. The results show a high retention of CO₂ in the gas hydrate phase with small pressure variations within the first hours. However, for our system containing 10.2 g of H₂O full conversion of the CH₄ hydrate grains to CO₂ hydrate is estimated to require 40 days. This delay is attributed to the shrinking core effect, where initially an outer layer of CO₂-rich hydrate is formed that effectively s... [more]

A considerable proportion (about 64%) of biomass energy is produced from woody biomass (wood and its wastes). However, waste wood (WW) is very often contaminated with metal(loid) elements at concentrations leading to toxicity emissions and damages to facilities during thermal conversion. Therefore, procedures for preventing and/or alleviating the negative impacts of these elements require further development, particularly by providing informative and supportive information regarding the phase transformations of the metal(loid)s during thermal conversion processes. Although it is well known that phase transformation depends on different factors such as elements’ vaporization characteristics, operational conditions, and process configuration; however, the influences of reaction atmosphere composition in terms of interactions and interferences are rarely addressed. In response, since Cu, Cr, and As (CCA-elements) are the most regulated elements in woody biomass, this paper aims to explore... [more]

Combustion tests and gaseous emissions of olive mill solid wastes pellets (olive pomace (OP), and olive pits (OPi)) were carried out in an updraft counter-current fixed bed reactor. Along the combustion chamber axis and under a constant primary air flow rate, the bed temperatures and the mass loss rate were measured as functions of time. Moreover, the gas mixture components such as O₂, organic carbon (Corg), CO, CO₂, H₂O, H₂, SO₂, and NOx (NO + NO₂) were analyzed and measured. The reaction front positions were determined as well as the ignition rate and the reaction front velocity. We have found that the exhaust gases are emitted in acceptable concentrations compared to the combustion of standard wood pellets reported in the literature (EN 303-5). It is shown that the bed temperature increased from the ambient value to a maximum value ranging from 750 to 1000 °C as previously reported in the literature. The results demonstrate the promise of using olive mill solid waste pellets as an a... [more]

We wish to correct Table 5 of the published paper in Processes [1].[...]

This paper presents an experimental study of the self-initiation reaction of n-butyl acrylate (n-BA) in free-radical polymerization. For the first time, the frequency factor and activation energy of the monomer self-initiation reaction are estimated from measurements of n-BA conversion in free-radical homo-polymerization initiated only by the monomer. The estimation was carried out using a macroscopic mechanistic mathematical model of the reactor. In addition to already-known reactions that contribute to the polymerization, the model considers a n-BA self-initiation reaction mechanism that is based on our previous electronic-level first-principles theoretical study of the self-initiation reaction. Reaction rate equations are derived using the method of moments. The reaction-rate parameter estimates obtained from conversion measurements agree well with estimates obtained via our purely-theoretical quantum chemical calculations.