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Lithium-ion batteries (LIBs) have gained much interest in recent years because of the increasing energy demand and the relentless progression of climate change. About 30% of the manufacturing cost for LIBs is spent on cathode materials, and its level of development is lower than the negative electrode, separator diaphragm and electrolyte, therefore becoming the "controlling step". Numerous cathodic materials have been employed, LiFePO 4 being the most relevant one mainly because of its excellent performance, as well as its rated capacity (170 mA·h·g -1 ) and practical operating voltage (3.5 V vs. Li + /Li). Nevertheless, producing micro and nanoparticles with high purity levels, avoiding the formation of iron oxides, and reducing the operating cost are still some of the aspects still to be improved. In this work, we have applied two heating rates (slow and fast) to the same hydrothermal synthesis process with the main objective of obtaining, without any reducing agents, the purest possible LiFePO 4 in the shortest time and with the lowest proportion of magnetite impurities. The reagents initially used were: FeSO 4 , H 3 PO 4 , and LiOH, and a crucial phenomenon has been observed in the temperature range between 130 and 150 °C, being verified with various techniques such as XRD and SEM.

Studies on the development and evolution of anaerobic digestion (AD) pretreatments are nowadays becoming widespread, due to the outstanding benefits that these processes could entail in the management of sewage sludge. Production of sewage sludge in wastewater treatment plants (WWTPs) is becoming an extremely important environmental issue. The work presented in this paper is a continuation of our previous studies with the aim of understanding and developing the advanced thermal hydrolysis (ATH) process. ATH is a novel AD pretreatment based on a thermal hydrolysis (TH) process plus hydrogen peroxide (H2O2) addition that takes advantage of a peroxidation/direct steam injection synergistic effect. The main goal of the present research was to compare the performance of TH and ATH, conducted at a wide range of operating conditions, as pretreatments of mesophilic AD with an emphasis on methane production enhancement as a key parameter and its connection with the sludge solubilization. Results showed that both TH and ATH patently improved methane production in subsequent mesophilic BMP (biochemical methane potential) tests in comparison with BMP control tests (raw secondary sewage sludge). Besides other interesting results and discussions, a promising result was obtained since ATH, operated at temperature (115 °C), pretreatment time (5 min) and pressure (1 bar) considerably below those typically used in TH (170 °C, 30 min, 8 bar), managed to enhance the methane production in subsequent mesophilic BMP tests [biodegradability factor (fB) = cumulative CH4production/cumulative CH4production (Control) = 1.51 ± 0.01] to quite similar levels than conventional TH pretreatment [fB = 1.52 ± 0.03]., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

The aim of this work was to study in depth the behavior and optimization of a novel process, called advanced thermal hydrolysis (ATH), to determine its utility as a pretreatment (sludge solubilization) or postreatment (organic matter removal) for anaerobic digestion (AD) in the sludge line of wastewater treatment plants (WWTPs). ATH is based on a thermal hydrolysis (TH) process plus hydrogen peroxide (H(2)O(2)) addition and takes advantage of a peroxidation/direct steam injection synergistic effect. On the basis of the response surface methodology (RSM) and a modified Doehlert design, an empirical second-order polynomial model was developed for the total yield of: (a) disintegration degree [DD (%)] (solubilization), (b) filtration constant [F(c) (cm(2)/min)] (dewaterability), and (c) organic matter removal (%). The variables considered were operation time (t), temperature reached after initial heating (T), and oxidant coefficient (n = oxygen(supplied)/oxygen(stoichiometric)). As the model predicts, in the case of the ATH process with high levels of oxidant, it is possible to achieve an organic matter removal of up to 92%, but the conditions required are prohibitive on an industrial scale. ATH operated at optimal conditions (oxygen amount 30% of stoichiometric, 115 °C and 24 min) gave promising results as a pretreatment, with similar solubilization and markedly better dewaterability levels in comparison to those obtained with TH at 170 °C. The empirical validation of the model was satisfactory.

The aim of this work is to present the application of the hydrothermal oxidation in supercritical conditions, also named supercritical water oxidation (SCWO) to the treatment of two commercial cutting fluids: Biocut and Servol. Experiments were carried out in a continuous flow system at a constant pressure of 25 MPa, using pure oxygen as oxidant in excess, and different temperatures ranging from 673 to 773 K. Both semi-synthetic cutting fluids are a mixture of several compounds so the efficiency of the oxidation process was followed in terms of the reduction in chemical oxygen demand (COD) and total organic carbon (TOC). A comparison of the results obtained in the study showed that it is possible to apply successfully SCWO for both cutting fluids, obtaining more than 95% for both COD and TOC removal at 773 K. However, the results also show that different residence times are needed to obtain the same percentage of COD or TOC removal depending on the cutting fluid treated, being in all cases Servol easier to oxidize than Biocut. A kinetic model to predict COD and TOC conversion has been proposed for both cutting fluids. A two-parameter mathematical model involving two steps (a fast reaction followed by a slow reaction) was used to describe the Biocut SCWO kinetics and to calculate the kinetic constants.