Design, commissioning and start-up of a new hydrothermal liquefaction continuous pilot unit

Hydrothermal liquefaction (HTL) has been demonstrated to be an effective emerging technology for the conversion of various biomass slurries into valuable biofuels and bioproducts precursors. Many studies have been carried out in batch laboratory-scale apparatus, an effective technique to understand the conversion process applied on several wet materials, from algae to organic wastes and lignocellulosic streams. On the other hand, some examples of continuous system have been implemented and tested worldwide as first step for the industrial scale-up of the technology. This work focuses on the development from the design to the start-up and commissioning of a new continuous HTL unit, established in RE-CORD laboratories. The plant is capable of converting 1-2 kg/hof slurry at about 10 wt.% of biomass to water ratio. The hydrothermal conversion unit comprises a high−pressure slurry feeder, an indirectly heated plug flow reactor, a cooling system, a pressure let-down system and liquid-gas separator. The reactor can reach and keep the converting material at 350 °C at a pressure of 220 bar for a residence time of 5 to 24 min. The solid content can be filtered in-line or separated at the end of the process depending on the physical characteristics of the suspended solid residues. Two different depressurizing system have been designed and implemented in parallel for the continuous discharge of the liquid products, widening the operability of the system to a larger selection of feedstock. The plant commissioning allowed to assess the process analysis in term of heating, pressurizing and reaction control. Flow rate, temperature and pressure profiles along the reaction and cooling zones have been acquired by a National Instrument data acquisition system. The software for data acquisition and for the control of the heaters and the depressurizing system was internally developed with NI LabVieW

Hydrothermal depolymerization of biorefinery lignin-rich streams: Influence of reaction conditions and catalytic additives on the organic monomers yields in biocrude and aqueous phase

Hydrothermal depolymerization of lignin-rich streams (LRS) from lignocellulosic ethanol was successfully carried out in a lab-scale batch reactors unit. A partial depolymerization into oligomers and monomers was achieved using subcritical water as reaction medium. The influence of temperature (300–350–370 °C) and time (5–10 minutes) was investigated to identify the optimal condition on the monomers yields in the lighter biocrude (BC1) and aqueous phase (AP) fractions, focusing on specific phenolic classes as well as carboxylic acids and alcohols. The effect of base catalyzed reactions (2–4 wt. % of KOH) was compared to the control tests as well as to acid-catalyzed reactions obtained with a biphasic medium of supercritical carbon dioxide (sCO2) and subcritical water. KOH addition resulted in enhanced overall depolymerization without showing a strong influence on the phenolic generation, whereas sCO2 demonstrated higher phenolic selectivity even though no effect was observed on the overall products mass yields. In conclusion, a comparison between two different biocrude collection procedures was carried out in order to understand how the selected chemical extraction mode influences the distribution of compounds between BC1 and AP

Lab-scale pyrolysis and hydrothermal carbonization of biomass digestate: Characterization of solid products

The aim of the present study is to investigate the production of biochar from anaerobic digestion (AD) digestate. Re-Cord selected digestate from real and representative (regarding the scale and the process technology) anaerobic digestion plant. Please click on the file below for full content of the abstract

Conceptual design and techno-economic assessment of coupled hydrothermal liquefaction and aqueous phase reforming of lignocellulosic residues

Hydrothermal liquefaction is a promising technology for producing renewable advanced biofuels. However, some weaknesses could undermine its large-scale application, such as the significant carbon loss in the aqueous phase (AP) and the necessity of biocrude upgrading. In order to deal with these challenges, in this work the techno-economic feasibility of coupling hydrothermal liquefaction (HTL) with aqueous phase reforming (APR) was evaluated. APR is a catalytic process able to convert water-dissolved oxygenates into a hydrogen-rich gas that can be used for biocrude upgrading. Two cases were proposed, based on different lignocellulosic feedstocks: corn stover (CS) and lignin-rich stream (LRS) from cellulosic ethanol production. HTL-APR plants operating with the same mass flow (3.6 t/h) at 10 wt% solid loading were herein evaluated, resulting in an input size of 20 MW (LRS) and 16.5 MW (CS). Based on experimental and literature data, the mass and energy balances were per- formed; subsequently, the main equipment was designed; finally, the capital and operating costs were evaluated. The analysis showed that the minimum selling prices for the biofuel (0% internal rate of return) were 1.23 (LRS) and 1.27 €/kg (CS). The heat exchangers accounted for most of the fixed capital investment, while electricity and feedstock had the highest impact on the operating costs. The implementation of APR was particularly profitable with CS, as it produced 107% of the hydrogen required for biocrude upgrading. In this case, APR was able to significantly reduce the H2 production cost (1.5 €/kg) making it a competitive technology compared to con- ventional electrolysis

Jean-Martin Charcot’s role in the 19th century study of music aphasia

Jean-Martin Charcot (1825–93) was a well-known French neurologist. Although he is widely recognized for his discovery of several neurological disorders and his research into aphasia, Charcot’s ideas about how the brain processes music are less well known. Charcot discussed the music abilities of several patients in the context of his ‘Friday Lessons’ on aphasia, which took place at the Salpêtrière Hospital in Paris in 1883–84. In his most comprehensive discussion about music, Charcot described a professional trombone player who developed difficulty copying music notation and playing his instrument, thereby identifying a new isolated syndrome of music agraphia without aphasia. Because the description of this case was published only in Italian by one of his students, Domenico Miliotti, there has been considerable confusion and under-acknowledgement of Charcot’s ideas about music and the brain. In this paper, we describe Charcot’s ideas regarding music and place them within the historical context of the growing interest in the neurological underpinnings of music abilities that took place in the 1880s

Music, neurology, and psychology in the nineteenth century

This chapter examines connections between research in music, neurology, and psychology during the late-nineteenth century. Researchers in all three disciplines investigated how music is processed by the brain. Psychologists and comparative musicologists, such as Carl Stumpf, thought in terms of multiple levels of sensory processing and mental representation. Early thinking about music processing can be linked to the start of Gestalt psychology. Neurologists such as August Knoblauch also discussed multiple levels of music processing, basing speculation on ideas about language processing. Knoblauch and others attempted to localize music function in the brain. Other neurologists, such as John Hughlings Jackson, discussed a dissociation between music as an emotional system and language as an intellectual system. Richard Wallaschek seems to have been the only one from the late-nineteenth century to synthesize ideas from musicology, psychology, and neurology. He used ideas from psychology to explain music processing and audience reactions and also used case studies from neurology to support arguments about the nature of music. Understanding the history of this research sheds light on the development of all three disciplines—musicology, neurology, and psychology.https://digitalcommons.chapman.edu/music_books/1000/thumbnail.jp

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TCC (graduação) - Universidade Federal de Santa Catarina. Centro de Comunicação e Expressão. Jornalismo.Investigar o uso de animais nas aulas práticas de medicin

Platinum-Group Minerals in Chromitites of the Niquelândia Layered Intrusion (Central Goias, Brazil): Their Magmatic Origin and Low-Temperature Reworking during Serpentinization and Lateritic Weathering

A variety of platinum-group-minerals (PGM) have been found to occur associated with the chromitite and dunite layers in the Niquelândia igneous complex. Two genetically distinct populations of PGM have been identified corresponding to phases crystallized at high temperatures (primary), and others formed or modified during post-magmatic serpentinization and lateritic weathering (secondary). Primary PGM have been found in moderately serpentinized chromitite and dunite, usually included in fresh chromite grains or partially oxidized interstitial sulfides. Due to topographically controlled lateritic weathering, the silicate rocks are totally transformed to a smectite-kaolinite-garnierite-amorphous silica assemblage, while the chromite is changed into a massive aggregate of a spinel phase having low-Mg and a low Fe3+/Fe2+ ratio, intimately associated with Ti-minerals, amorphous Fe-hydroxides, goethite, hematite and magnetite. The PGM in part survive alteration, and in part are corroded as a result of deep chemical weathering. Laurite is altered to Ru-oxides or re-crystallizes together with secondary Mg-ilmenite. Other PGM, especially the Pt-Fe alloys, re-precipitate within the altered chromite together with kaolinite and Fe-hydroxides. Textural evidence suggests that re-deposition of secondary PGM took place during chromite alteration, controlled by variation of the redox conditions on a microscopic scale