Non-structural applications of Ioncell® carbon fibers

Engineering cellulose-based materials has received much attention to relieve the burden of CO2 emissions and dependence on non-renewable resources. In particular, as this thesis demonstrates, cellulose pyrolysis represents a potential route to fabricate carbon fibers (CF), which can alleviate the global demand for natural graphite and synthetic carbons. Nevertheless, understanding cellulose thermal decomposition presents many knowledge gaps; filling them is necessary to tailor CF that display specific nanostructures, functionalities, and textures. The work hereafter examined the carbonization yield y1 of Ioncell® cellulose fibers. y1 is a constraint hindering the scalability of cellulose as a CF precursor. This thesis displays how experimental design can assist in modeling the influence of diammonium hydrogen phosphate (DAP), CO2 activation time, and lignin (BL) on cellulose y1. DAP and BL are factors known for increasing y1 as they inhibit forming small volatile carbon compounds during cellulose pyrolysis. However, this study showed that, when combined, the effect of DAP and BL on y1 are non-additive. Assessing the performance of Ioncell CF in non-structural applications consisted of enhancing their texture and surface chemistry. This thesis bridged gaps in carbon materials science during the CF characterization. For example, the manuscript adapts and verifies tools and methods developed by third-parties to ease the mathematical treatment of adsorption isotherms and Raman spectra. All in all, Ioncell CF had relatively high CO2 adsorptions (~2 mmol/g) at unsaturated pressure conditions. These biobased CF were microporous materials, and they may be crucial in gas separation membranes and storage systems

4to. Congreso Internacional de Ciencia, Tecnología e Innovación para la Sociedad. Memoria académica

Este volumen acoge la memoria académica de la Cuarta edición del Congreso Internacional de Ciencia, Tecnología e Innovación para la Sociedad, CITIS 2017, desarrollado entre el 29 de noviembre y el 1 de diciembre de 2017 y organizado por la Universidad Politécnica Salesiana (UPS) en su sede de Guayaquil. El Congreso ofreció un espacio para la presentación, difusión e intercambio de importantes investigaciones nacionales e internacionales ante la comunidad universitaria que se dio cita en el encuentro. El uso de herramientas tecnológicas para la gestión de los trabajos de investigación como la plataforma Open Conference Systems y la web de presentación del Congreso http://citis.blog.ups.edu.ec/, hicieron de CITIS 2017 un verdadero referente entre los congresos que se desarrollaron en el país. La preocupación de nuestra Universidad, de presentar espacios que ayuden a generar nuevos y mejores cambios en la dimensión humana y social de nuestro entorno, hace que se persiga en cada edición del evento la presentación de trabajos con calidad creciente en cuanto a su producción científica. Quienes estuvimos al frente de la organización, dejamos plasmado en estas memorias académicas el intenso y prolífico trabajo de los días de realización del Congreso Internacional de Ciencia, Tecnología e Innovación para la Sociedad al alcance de todos y todas

Interdependent factors influencing the carbon yield, structure, and CO2 adsorption capacity of lignocellulose-derived carbon fibers using multiple linear regression

| openaire: EC/H2020/715788/EU//WoCaFi Funding Information: Open Access funding provided by Aalto University. The research was supported by European Union’s Horizon 2020 research and innovation programme [715788] and the Academy of Finland (Elucidation of the structural development during cellulose carbonization for advanced carbon materials) [348354]. Publisher Copyright: © 2023, The Author(s).Cellulose has experienced a renaissance as a precursor for carbon fibers (CFs). However, cellulose possesses intrinsic challenges as precursor substrate such as typically low carbon yield. This study examines the interplay of strategies to increase the carbonization yield of (ligno-) cellulosic fibers manufactured via a coagulation process. Using Design of Experiments, this article assesses the individual and combined effects of diammonium hydrogen phosphate (DAP), lignin, and CO2 activation on the carbonization yield and properties of cellulose-based carbon fibers. Synergistic effects are identified using the response surface methodology. This paper evidences that DAP and lignin could affect cellulose pyrolysis positively in terms of carbonization yield. Nevertheless, DAP and lignin do not have an additive effect on increasing the yield. In fact, combined DAP and lignin can affect negatively the carbonization yield within a certain composition range. Further, the thermogravimetric CO2 adsorption of the respective CFs was measured, showing relatively high values (ca. 2 mmol/g) at unsaturated pressure conditions. The CFs were microporous materials with potential applications in gas separation membranes and CO2 storage systems. Peer reviewe

Thermal gelation of cellulose based suspensions

Funding Information: Open Access funding provided by Aalto University. J. K. acknowledges funding from Academy of Finland (308235). M. J. A., A. P. and J. K. acknowledge support from FinnCERES flagship (151830423), Business Finland (211835) and Future Makers (Älyä Vaahtoihin) programs. Publisher Copyright: © 2023, The Author(s).A more sustainable future calls for bio-based alternatives to replace plastic foams for various applications, such as packaging, insulation and cushioning. Some bio-based foams emerging in scientific publications are fabricated using liquid foam templating and methyl cellulose as well as fibers as main constituents. Scaling up of the production, however, requires a comprehensive understanding of the rheology of the foam during the shaping and drying processes. In this article, we report rheological studies of cellulose based systems in the context of thermal gelation. In more precise terms, we study how the presence of cellulose fibers and other additive materials influences the thermal gelation properties of methyl cellulose. We observe that the rheological properties, while heavily dependent on the material composition, are reasonably adjustable by appropriate material choices. The fibers are seen to decrease the temperature required for methyl cellulose to undergo a viscoelastic transition which is useful in the solid foam fabrication process. We anticipate that in the present application, the fibers increase the stability of the desired structure during the drying stage of the foam.Peer reviewe

Reinvestigating the concurring reactions in early-stage cellulose pyrolysis by solution state NMR spectroscopy

Low temperature pre-treatments increase the char yield during cellulose carbonization. Although this effect is mostly understood on a kinetic basis, the formed chemical structures leave room for scrutiny. In ongoing ambitions to enhance the char yield of bioderived precursors, the thereby occurring chemistry was reinvestigated. A set of isothermal heating protocols ranging from 150° to 250°C was applied to man-made Ioncell® cellulose fibers and to Avicel® PH-101 microcrystalline cellulose. The prepared cellulosic samples were examined by solution state NMR using a tetra-n-butyl phosphonium acetate ([P4444][OAc]): DMSO-d6 (1:4 wt%) electrolyte as dissolving medium. Complementary, IR spectroscopy, size-exclusion chromatography (SEC) and thermogravimetric analysis coupled with mass spectroscopy (TGA-MS) measurements were performed. The NMR spectra evidenced the formation of levoglucosan end capped moieties as being the first and major occurring reaction during low temperature pre-treatments. In contrast to other mechanistic proposals, no signs for carbonyl or alkene functionalities were discernible in the cellulosic material soluble in the NMR electrolyte, even after treatment at 250 °C for several hours. Thermal cross-linking was observed in SEC already at temperatures not known to significantly influence the overall char yield. In the solution state analytics only partial solubility was observed, owing to the formation of a reluctant fraction previously described as “thermostable condensed phase”. This resulted in analytical blind spots and led to discrepancies between NMR results and FTIR spectra in which carbonyl and alkene vibrations were clearly discernible. Those discrepancies might also imply the co-existence of different fractions in the early stages of cellulose pyrolysis.</p

Predicting effect of fibers on thermal gelation of methylcellulose using Bayesian optimization

Understanding of the viscoelastic behavior of a polymer is a prerequisite for its thermomechanical processing beyond laboratory scale. Utilizing rheological characterization is a powerful tool to comprehend the complex nature and time-dependent properties of macromolecular materials. Nevertheless, it consumes time as rheometry involves iterating experiments under several conditions to visualize the non-linear behavior of materials under varying conditions. The work hereunder examines the rheology of cellulosic aqueous suspensions prepared using cellulose fibers as the dispersed phase (Refcell and Storacell) and methylcellulose (MC) as the polymeric matrix. Interfacial phenomena between MC and cellulose fibers arise in particle laden systems with supramolecular structures formed by non-covalent interactions. Therefore, this study elucidates the rheological evolution of these interactions as a function of temperature and fiber concentration. This study displays how researchers may reduce the number of rheological experiments and save time utilizing a novel method based on a Bayesian optimization with Gaussian processes.Peer reviewe

Cellulose foams as scalable templates for phase change materials

Funding Information: M. Alava and J. Koivisto acknowledge support from FinnCERES flagship [ 151830423 ] and Business Finland [ 211835 ]. M. Alava, T. Mäkinen and I. Y. Miranda-Valdez acknowledge support from Business Finland [ 211909 ]. M. R. Yazdani acknowledges financial support from the Academy of Finland [ 343192 ]. I. Y. Miranda-Valdez acknowledges financial support from the Finnish Ministry of Education and Culture via its Finland Fellowship scholarship program. The funding sources had no role in any activity related to this manuscript. Publisher Copyright: © 2023 The Author(s)Cellulose foams produced by wet-templating fibers and surfactants offer an unlimited creative space for the design of green functional materials with a wide range of energy-related applications. Aiming to reduce plastic pollution, cellulose foams promise to replace plastic foams after tailoring physical functionalities into their structures. Here, this work demonstrates that cellulose foams made of methylcellulose and cellulose fibers can exhibit a solid–liquid phase change functionality by adding a phase change material (PCM) during the foam-forming process. The resulting foam composites, termed cellulose phase change foams (PCFs), exhibit a tenth of cellulose's density (134.7 kg m−3) yet a high Young's modulus (0.42MPa). They are also dimensionally stable over a wide range of temperatures while absorbing up to 108 kJ kg−1 as latent heat when the PCM confined to the foam experiences a solid-to-liquid transition at ∼60 °C, and releasing 108 kJ kg−1 as latent heat when changing from liquid to solid at ∼40 °C. Such phase change transition opens up broad applications for the PCFs as thermal insulators. For example, by further tuning the transition temperature, the PCFs can exploit their phase change and reduce the heat flow rate through their radial direction at specified temperatures. This article showcases the versatility of the foam-forming process of cellulose to accommodate physical functionalities in materials with complex architectures. Furthermore, thanks to the advances in cellulose foam-forming, such foams are recyclable, industrially scalable, and can be exploited as heat storage materials.Peer reviewe

Viscoelastic phenomena in methylcellulose aqueous systems:Application of fractional calculus

Fractional calculus models can potentially describe the viscoelastic phenomena in soft solids. Nevertheless, their successful application is limited. This paper explored the potential of using fractional calculus models to describe the viscoelastic properties of soft solids, focusing on methylcellulose aqueous systems. Methylcellulose is an important food additive, and it is known for its complex rheological behaviors, including thermogelation, which still puzzle rheologists. Through dynamic mechanical analysis and fractional rheology, we demonstrated that fractional calculus described the frequency- and temperature-dependent rheology of methylcellulose. This paper also showcased how including one springpot could potentially replace numerous spring-dashpot arrangements. Our findings using fractional calculus suggested that the thermogelation of methylcellulose involves the cooperative mobility of polymer chains and can be described as a process analogous to the glass transition in polymers. This study highlighted the power of combining fractional calculus and rheology to understand complex viscoelastic phenomena in soft solids.</p

Viscoelastic phenomena in methylcellulose aqueous systems:Application of fractional calculus

Fractional calculus models can potentially describe the viscoelastic phenomena in soft solids. Nevertheless, their successful application is limited. This paper explored the potential of using fractional calculus models to describe the viscoelastic properties of soft solids, focusing on methylcellulose aqueous systems. Methylcellulose is an important food additive, and it is known for its complex rheological behaviors, including thermogelation, which still puzzle rheologists. Through dynamic mechanical analysis and fractional rheology, we demonstrated that fractional calculus described the frequency- and temperature-dependent rheology of methylcellulose. This paper also showcased how including one springpot could potentially replace numerous spring-dashpot arrangements. Our findings using fractional calculus suggested that the thermogelation of methylcellulose involves the cooperative mobility of polymer chains and can be described as a process analogous to the glass transition in polymers. This study highlighted the power of combining fractional calculus and rheology to understand complex viscoelastic phenomena in soft solids.</p