Relevant bibliographies by topics / Organosol

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Organosol'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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Journal articles on the topic "Organosol"

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Mohd Hirmizi, N. H., M. Abu Bakar, W. L. Tan, N. H. H. Abu Bakar, J. Ismail, and C. H. See. "Electrical and Thermal Behavior of Copper-Epoxy Nanocomposites Prepared via Aqueous to Organic Phase Transfer Technique." Journal of Nanomaterials 2012 (2012): 1–11. http://dx.doi.org/10.1155/2012/219073.

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The preparation, electrical, and thermal behaviors of copper-epoxy nanocomposites are described. Cetyltrimethylammonium bromide- (CTAB-) stabilized copper (Cu) particles were synthesized via phase transfer technique. Isopropanol (IPA), sodium borohydride (NaBH4), and toluene solution of diglycidyl ether of bisphenol A (DGEBA) were used as transferring, reducing agent, and the organic phase, respectively. The UV-Vis absorbance spectra of all the sols prepared indicate that the presence of Cu particles with the particles transfer efficiency is ≥97%. The amount, size, and size distribution of particles in the organosol were dependent on the content of organic solute in the organosol. The composites were obtained upon drying the organosols and these were then subjected to further studies on the curing, thermal, and electrical characteristic. The presence of Cu fillers does not significantly affect the completeness of the composite curing process and only slightly reduce the thermal stability of the composites that is >300°C. The highest conductivity value of the composites obtained is3.06×10-2 S cm-1.
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Curtis, Andrew C., Daniel G. Duff, Peter P. Edwards, David A. Jefferson, Brian F. G. Johnson, Angus I. Kirkland, and Andrew S. Wallace. "A Morphology-Selective Copper Organosol." Angewandte Chemie International Edition in English 27, no. 11 (November 1988): 1530–33. http://dx.doi.org/10.1002/anie.198815301.

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Curtis, Andrew C., Daniel G. Duff, Peter P. Edwards, David A. Jefferson, Brian F. G. Johnson, Angus I. Kirkland, and Andrew S. Wallace. "Ein Kupfer-Organosol mit wohldefinierter Morphologie." Angewandte Chemie 100, no. 11 (November 1988): 1588–90. http://dx.doi.org/10.1002/ange.19881001122.

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Ede, Sivasankara Rao, S. Anantharaj, U. Nithiyanantham, and Subrata Kundu. "DNA-encapsulated chain and wire-like β-MnO2 organosol for oxidative polymerization of pyrrole to polypyrrole." Physical Chemistry Chemical Physics 17, no. 7 (2015): 5474–84. http://dx.doi.org/10.1039/c4cp04236k.

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Anantharaj, S., U. Nithiyanantham, Sivasankara Rao Ede, E. Ayyappan, and Subrata Kundu. "π-stacking intercalation and reductant assisted stabilization of osmium organosol for catalysis and SERS applications." RSC Advances 5, no. 16 (2015): 11850–60. http://dx.doi.org/10.1039/c4ra15521a.

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Size-selective, mono-dispersed osmium organosol have been synthesized in toluene which is stabilized by π-stacking intercalation and electrostatic interactions for application in catalysis and SERS studies.
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Xiaochun, Wu, Wang Rongyao, Zou Bingsuo, Wang Li, Liu Shaomei, Xu Jiren, and Huang Wei. "Optical properties of nanometer-sized CdO organosol." Journal of Materials Research 13, no. 3 (March 1998): 604–9. http://dx.doi.org/10.1557/jmr.1998.0077.

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In this paper, nanometer-sized CdO organosol was prepared by using microemulsion methods. Its electronic structure and optical properties are characterized through UV-visible light absorption, photoluminescence, and Z-scan techniques. Some newfeatures were observed. Fluorescence and nonlinear optical responses are mainly related to surface trapped states.
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Mchedlov-Petrossyan, Nikolay O., Nika N. Kamneva, Younis T. M. Al-Shuuchi, Andriy I. Marynin, Olexii S. Zozulia, Alexander P. Kryshtal, Vladimir K. Klochkov, and Sergey V. Shekhovtsov. "Towards better understanding of C60organosols." Physical Chemistry Chemical Physics 18, no. 4 (2016): 2517–26. http://dx.doi.org/10.1039/c5cp06806a.

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The C60colloidal species in acetonitrile are negatively charged owing to formation of anion-radicals. Electrolytes coagulate the organosol, and multi-charged cations cause the re-charging of the particles.
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Ganguly, Mainak, Anjali Pal, and Tarasankar Pal. "Purification of Gold Organosol by Solid Reagent." Journal of Physical Chemistry C 116, no. 16 (April 17, 2012): 9265–73. http://dx.doi.org/10.1021/jp2121356.

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Ichiba, Sumio, and Toshio Sakamoto. "Mössbauer Emission Spectra of119mSn in Tin Organosol." Bulletin of the Chemical Society of Japan 58, no. 4 (April 1985): 1323–24. http://dx.doi.org/10.1246/bcsj.58.1323.

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Li, Yanping, Huangzhong Yu, Xinxin Huang, Zuping Wu, and Mingdong Chen. "A simple synthesis method to prepare a molybdenum oxide hole-transporting layer for efficient polymer solar cells." RSC Advances 7, no. 13 (2017): 7890–900. http://dx.doi.org/10.1039/c7ra00303j.

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We report a simple synthetic method to prepare amorphous molybdenum oxide (p-MoO3) using a favorably stable peroxomolybdic acid organosol as the precursor solution prepared by an ultrasonic reaction for the first time.
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Dissertations / Theses on the topic "Organosol"

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Silva, Pedro Henrique Fernandes. "Fracionamento da biomassa lignocelulósica pelo processo organosolv." reponame:Repositório Institucional da UnB, 2017. http://repositorio.unb.br/handle/10482/23561.

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Dissertação (mestrado)—Universidade de Brasília, Instituto de Química, Programa de Pós-Graduação em Tecnologias Química e Biológica, 2017.
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A biomassa tem ganhado destaque como matéria-prima renovável para obtenção de produtos químicos e energia, frente a uma competitiva indústria baseada em fontes fósseis. No Brasil, a biomassa florestal é largamente cultivada, seja na construção civil e fabricação de móveis, ou na produção de energia e na produção do papel. O eucalipto é a biomassa florestal de maior relevância em termos de cultivo no Brasil (38,1 m³/ha/ano no ano de 2015) e no mundo. Nas últimas décadas, têm-se buscado a desconstrução da biomassa lignocelulósica, como a madeira, em seus polímeros constituintes, a celulose, a hemicelulose e a lignina, de forma que cada uma possa ser processada de forma a gerar produtos de maior valor agregado. Neste contexto temos o processo organosolv, que é um pré-tratamento da biomassa lignocelulósica com a mistura de solventes orgânicos e água em elevadas temperaturas. Além de fracionar a biomassa, é possível se obter a partir do processo organosolv, componentes com elevado grau de pureza e mais reativos para futuras aplicações. O presente trabalho teve como objetivo estudar o efeito da temperatura (avaliada entre 180 °C e 220 °C) e relação etanol/água (avaliada entre 30% e 70% v/v) no processo organosolv aplicados a amostras de Eucalyptus grandis, sendo observado quanto de cada um dos polímeros foi removido da amostra sólida inicial. Os experimentos foram realizados segundo um planejamento experimental fatorial 22 com ponto central, com triplicata em todos os pontos. Como resultado foi obtido que o melhor ponto foi na condição experimental E(50,200) (relativo a 50% etanol e 200 °C), com 80,36% de lignina extraída e 91,35% de rendimento da celulose.
Biomass has gained prominence as a renewable raw material for obtaining chemicals and energy, in front of a competitive industry based on fossil sources. In Brazil, forest biomass is widely cultivated, whether in the construction and manufacturing of furniture, or in energy production and paper production. Eucalyptus is the most important forest biomass in terms of cultivation in Brazil (38.1 m³ / ha / year in 2015) and in the world. In the last decades, we have sought to deconstruct lignocellulosic biomass, such as wood, in its constituent polymers, cellulose, hemicellulose and lignin, so that each can be processed in order to generate products with higher benefit. In this context, we have the organosolv process, which is a pretreatment of the lignocellulosic biomass with the mixture of organic solvents and water at high temperatures. In addition to fractionating biomass, it is possible to obtainm from the organosolv process, components with high purity and more reactive for future applications. The objective of this work was to study the effect of temperature (evaluated between 180 °C and 220 °C) and ethanol / water ratio (evaluated between 30% and 70% v/v) in the organosolv process applied to samples of Eucalyptus grandis, being observed how much of each of the polymers was removed from the initial solid sample. The experiments were performed according to a factorial 22 experimental design with center point, with triplicate at all points. As a result it was obtained that the best point was in the experimental condition E(50,200) (relative to 50% ethanol and 200 °C), with 80.36% lignin extracted and 91.35% cellulose yield.
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Yawalata, Dominggus. "Catalytic selectivity in alcohol organosolv pulping of spruce wood." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/NQ61209.pdf.

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Bianchi, Maria Lucia. "Polpação de palha de milho, utilizando-se diferentes processos organosolv." [s.n.], 1995. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249491.

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Orientador: Ulf F. Schuchardt
Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Quimica
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Muurinen, E. (Esa). "Organosolv pulping:a review and distillation study related to peroxyacid pulping." Doctoral thesis, University of Oulu, 2000. http://urn.fi/urn:isbn:9514256611.

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Abstract More than 900 papers related to organosolv pulping have been reviewed in this thesis. From the information included in those papers it can be concluded that organosolv pulping processes are still in a developing stage and are not yet ready to seriously threat the position of the kraft process as the main pulp manufacturing process in the world. Distillation seems to be the main alternative as the process for recovering the solvent in organosolv pulping. A good reason for this is that using simple distillation no potentially harmful components are introduced to the process. The effect of feed composition on the operation of a separation sequence in an organosolv process using aqueous formic and acetic acids and corresponding peroxyacids was studied. When simple distillation was used as the separation method the effect was found to be significant. The no ideal nature of the formic acid-acetic acid-water mixture, which separation was studied, makes the ternary composition space to divide into four distillation regions. Which region the feed is located in, obviously determines the economy of the distillation sequence. Shortcut calculation methods cannot be recommended to be used for designing a distillation sequence for the ternary mixture studied, but they give useful information for the comparison of such sequences. They were used to choose a limited number of alternatives for studies with rigorous calculation methods. Minimum work of separation can also be used to make a satisfying estimate for the relative easiness of separation of the formic acid-acetic acid-water mixture. Thermal integration using pinch technology was also tested and found very useful for decreasing the thermal energy consumption of distillation processes. Thermodynamic efficiencies for separating the formic acid-acetic acid-water mixture by simple distillation were estimated. They were found to be lower than the average value for distillation presented in literature.
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Maza, Lisa Jésus. "Résines vertes à base de lignine organosolve." Thesis, Pau, 2017. http://www.theses.fr/2017PAUU3039.

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Les résines phénoliques, sont entre autres utilisées dans l’industrie du bois pour la fabrication de panneaux de particules ou de contreplaqués, après des étapes d'encollage, d'imprégnation et/ou de pressage à chaud. Elles sont principalement obtenues par polymérisation par étapes (polycondensation) à partir de formaldéhyde et de phénol. Ces deux matières premières de base sont actuellement des produits issus de la pétrochimie.Ce travail de thèse Cifre, en partenariat avec la société Rolkem, spécialisée dans la conception et la fabrication de résines phénoliques de type résol, a pour objectif la réduction de l’utilisation de matières pétrochimiques via la substitution du phénol par une bioressource telle que la lignine. Cette dernière a une structure phénolique et une similarité structurelle avec le réseau des résines phénoliques, elle est abondante dans la nature et disponible. Pour atteindre l’industrialisation de ces nouvelles résines biosourcées, une étude sur la compréhension des mécanismes réactionnels qui gouvernent le procédé a été menée avant d’optimiser le protocole permettant l’incorporation de la lignine dans les résines.Il a été possible de remplacer jusqu’à 50%m du phénol par de la lignine organosolve et de réduire la concentration initiale en formaldéhyde. En utilisant une lignine Kraft il a été possible de remplacer jusqu’à 75%m du phénol et de réduire jusqu’à 30%m du formaldéhyde utilisé, par rapport aux résines classiques de référence, tout en respectant le cahier des charges imposé par Rolkem. Ces résultats ont été possibles grâce à des suivis cinétiques des procédés et des études de réactivité de la lignine. Grâce à ces travaux de thèse, le transfert d’échelle des résines biosourcées du laboratoire au pilote industriel a été possible, tout en respectant les contraintes industrielles telles que la productivité, la qualité, la sécurité et l’environnement. De plus, les essais industriels de collage de contreplaqués réalisés sont conformes aux prérequis.En complément des objectifs fixés par le projet, et de manière plus académique, la réactivité de la lignine vis-à-vis du formaldéhyde a été étudiée en chauffage conventionnel et sous irradiation microonde. Cette étude complémentaire permet de corréler la réactivité lignine-formaldéhyde et mode de chauffage et d’atteindre spécifiquement des produits issus de réactions d’addition ou de condensation
Phenolic resins, may be used in the wood industry for the manufacture of particle boards or plywood, after gluing, impregnation and/or hot-pressing steps. They are mainly obtained by step polymerization (polycondensation) from formaldehyde and phenol. These two raw materials are currently petrochemicals.This thesis work, supported by Rolkem, a company specialized in the design and manufacture of resol type phenolic resins, aims to reduce the use of non-biobased materials by replacing phenol with lignin exhibiting a phenolic structure and a structural similarity with the network of phenolic resins. Lignin is abundant in the environment and easily available. To achieve the industrialization of these new biobased resins, a study on the understanding of the reaction mechanisms has been carried out to favor the incorporation of lignin within the resins. It has been possible to replace up to 50wt.% of the phenol with organosolve lignin and to reduce the initial concentration of formaldehyde at the same time. 75wt.% substitution has been achieved using a Kraft lignin by reducing up to 30wt.% of the formaldehyde concentration as compared to conventional resins. The new biobased resins respect the Rolkem specifications. Thanks to this work results, the scale transfer of biobased resins from the laboratory scale to the industrial pilot was possible, while respecting industrial constraints such as productivity, quality, safety and environment. In addition, the industrial plywood bonding tests were in accordance with the prerequisite.In addition to the above objectives the reactivity of BiolignineTM with formaldehyde has been studied under conventional heating and microwave irradiation. This complementary study allows the correlation of the lignine-formaldehyde reactivity and the heating modes to specifically reach products resulting from addition or condensation reactions
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Muurinen, Esa. "Organosolv pulping a review and distillation study related to peroxyacid pulping /." OuLu : Oulun yliopisto, 2000. http://catalog.hathitrust.org/api/volumes/oclc/47152371.html.

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Tan, Xin. "Effect of Organosolv Lignin and Extractable Lignin on Enzymatic Hydrolysis of Lignocelluloses." University of Cincinnati / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1613752000022518.

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Chao, Hsiu-Yi. "Luminescent organogold(I) complexes with electron rich bulky phosphine ligands : synthesis and spectroscopic studies /." Hong Kong : University of Hong Kong, 2001. http://sunzi.lib.hku.hk/hkuto/record.jsp?23242309.

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Hess, Fiona Millicent. "Halo- and organogold(I) complexes as potential metallomesogens." Master's thesis, University of Cape Town, 1999. http://hdl.handle.net/11427/9757.

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There is currently much interest in how the properties of liquid crystals may be altered by metal atoms. Gold(I) complexes of the type RAuL have recently been shown to exhibit interesting liquid crystal behaviour. As molecular structure and intermolecular forces play a major role in liquid crystal chemistry, changing the nature of the R and L groups result in changes mesomorphic properties. The aim of the project was to synthesise RAuL complexes with stilbazole ligands and to investigate how different R groups influence the liquid crystal properties. ClAu(n-OST) complexes, n-OST = trans-4,4'-alkoxystilbazole with n = number of carbon atoms in the alkoxy chain, were synthesised from ClAu(tht) and n-OST. They were found to exhibit smectic A mesophases, melting between 135-153 °C and decomposing at the clearing point at 168-180 °C. The transition temperatures decreased as the chain length of the n-OST ligand increased.
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Schwiderski, Martin [Verfasser], Herbert [Akademischer Betreuer] Vogel, and Andrea [Akademischer Betreuer] Kruse. "Aluminiumchlorid katalysierter Organosolv-Aufschluss von Lignocellulosen / Martin Schwiderski ; Herbert Vogel, Andrea Kruse." Darmstadt : Universitäts- und Landesbibliothek Darmstadt, 2017. http://d-nb.info/1131254201/34.

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Books on the topic "Organosol"

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Ariztegui, Aurelio Sagaseta. Organos de Navarra. [Pamplona]: Gobierno De Navarra, Departamento De Educacion Y Cultura, Institucion Principe De Viana, 1985.

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Spain. Organos constitucionales: Legislación electoral. Madrid: La Ley, 1992.

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Khan, Tasneem A. Chemistry of organogold (I) & (III) complexes. Manchester: UMIST, 1997.

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Paszner, Laszlo. Innovations for hardwood utilization: Catalysed organosolv pulping and saccharification. Edmonton: Forestry Canada, 1988.

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José Santos de la Iglesia Ugarte. Los organos en La Rioja. [La Rioja, Spain]: Gobierno de La Rioja, Consejeria de Cultura, Deportes y Juventud, 1991.

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Izcovich, Sara Gampel de. Enseñanza media: Organos colegiados de gobierno. Buenos Aires: Fundación Arturo Illia para la Democracia y la Paz, 1988.

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Parra, Gustavo Delgado. Organos históricos de Oaxaca: Estudio y catalogación. México, D.F: CONACULTA-INAH, 1999.

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Paredes, José Sánchez. Catálogo de los organos judiciales de España. 2nd ed. Lorca: J. Sánchez Paredes, 1992.

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Gafo, Javier, and Diego Gracia. Trasplantes de organos: Problemas tecnicos, eticos y legales. Madrid: Fundación Humanismo y Democracía, 1996.

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Gemert, Hans van. Organos históricos del Perú =: Historic organs of Peru. Hillbrow, Sudáfrica: H. van Gemert, 1990.

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Book chapters on the topic "Organosol"

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Gooch, Jan W. "Organosol." In Encyclopedic Dictionary of Polymers, 506. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_8245.

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Brosse, Nicolas, Mohd Hazwan Hussin, and Afidah Abdul Rahim. "Organosolv Processes." In Advances in Biochemical Engineering/Biotechnology, 153–76. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/10_2016_61.

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Krause, Norbert. "Organogold Chemistry." In Organometallics in Synthesis, 429–540. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118651421.ch4.

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Cook, Phillip M., and Terry Sellers. "Organosolv Lignin-Modified Phenolic Resins." In ACS Symposium Series, 324–33. Washington, DC: American Chemical Society, 1989. http://dx.doi.org/10.1021/bk-1989-0397.ch024.

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Pye, E. Kendall, and Michael Rushton. "Organosolv Biorefining: Creating Higher Value from Biomass." In Catalytic Process Development for Renewable Materials, 239–63. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527656639.ch9.

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Gonçalves, Adilson R., and Ulf Schuchardt. "Oxidation of Organosolv Lignins in Acetic Acid." In Twentieth Symposium on Biotechnology for Fuels and Chemicals, 127–32. Totowa, NJ: Humana Press, 1999. http://dx.doi.org/10.1007/978-1-4612-1604-9_12.

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Xu, Chunbao, Baoqiang Liao, and Wei Shi. "Organosolv Pretreatment of Pine Sawdust for Bio-ethanol Production." In Pretreatment Techniques for Biofuels and Biorefineries, 435–57. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-32735-3_19.

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Ruzene, Denise S., Adilson R. Gonçalves, José A. Teixeira, and Maria T. Pessoa de Amorim. "Carboxymethylcellulose Obtained by Ethanol/Water Organosolv Process Under Acid Conditions." In Applied Biochemistry and Biotecnology, 573–82. Totowa, NJ: Humana Press, 2007. http://dx.doi.org/10.1007/978-1-60327-181-3_47.

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Pan, Xuejun. "Organosolv Biorefining Platform for Producing Chemicals, Fuels, and Materials from Lignocellulose." In The Role of Green Chemistry in Biomass Processing and Conversion, 241–62. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118449400.ch7.

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Hergert, H. L., G. C. Goyal, and J. H. Lora. "Limiting Molecular Weight of Lignin from Autocatalyzed Organosolv Pulping of Hardwood." In ACS Symposium Series, 265–77. Washington, DC: American Chemical Society, 1999. http://dx.doi.org/10.1021/bk-2000-0742.ch012.

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Conference papers on the topic "Organosol"

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Wu, Xiaochun, Rongyao Wang, Li Wang, Shaomei Liu, and Bingsuo Zou. "Optical nonlinearity of nanometer-sized CdO organosol using Z-scan measurement." In Photonics China '96, edited by Ratnakar R. Neurgaonkar, Tsutomu Shimura, and Peixian Ye. SPIE, 1996. http://dx.doi.org/10.1117/12.253236.

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KOBETS, A., and T. VOROBYOVA. "ELECTROLESS NICKEL PLATING ON SILICATE GLASS SENSITIZED WITH Sn(II) CONTAINING ORGANOSOL." In Proceedings of International Conference Nanomeeting – 2011. WORLD SCIENTIFIC, 2011. http://dx.doi.org/10.1142/9789814343909_0088.

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Pals, Matiss, Liga Lauberte, Alexandr Arshanitsa, Laima Vevere, Vilhelmine Jurkjane, and Galina Telysheva. "Organosolv delignification of residual plantation willow bark after extractive removal." In Research for Rural Development 2020. Latvia University of Life Sciences and Technologies, 2020. http://dx.doi.org/10.22616/rrd.26.2020.011.

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Plantation willows are commonly grown plants which are widely used for energetic purposes that does not correspond completely to its potential. To fully integrate this resource into biorefinery scheme, it is necessary to study optimal conditions of willow bark processing, aimed for separation of bark components, their comprehensive characterization and profitable practical application. Extraction of secondary metabolites is well known approach for bark processing. But the separation of the main cell wall components including lignin from the residual biomass is less studied. In this work plantation residual willow bark after extractives separation by two different solvents (acetone and ethanolwater) was used as a feedstock for Organosolv delignification. Effect of temperature and catalyst used on the yield and properties of lignin isolated from residual bark by ethanol-water treatment was studied. It was possible to obtain pure lignin with high yields (up to 41%) that has the potential to be used for bio-plastic producing. Insoluble residue after delignification was carbohydrate rich (up to 80%) feedstock allowing its practical use for bioethanol producing.
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Pham, Q., N. Brosse, C. Frochot, and B. Jamart-Grégoire. "Self-Organization of Gelator Molecules Inside an Organogel." In 3rd France-Russia Seminar. Les Ulis, France: EDP Sciences, 2007. http://dx.doi.org/10.1051/names2007030.

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Sidiras, Dimitrios, Ioanna Salapa, and Dorothea Politi. "Organosolv Modified Wheat Straw as Adsorbent for Basic Dyes in Water Bodies." In The 2nd World Congress on Mechanical, Chemical, and Material Engineering. Avestia Publishing, 2016. http://dx.doi.org/10.11159/iccpe16.106.

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Al Afif, Rafat, Martin Wendland, Lutz Christian Krapf, Thomas Amon, and Christoph Pfeifer. "Organosolv Plus Supercritival Carbon Dioxide Pre-Treatment of Cotton Stalks for Methane Production." In 10TH International Conference on Sustainable Energy and Environmental Protection. University of Maribor Press, 2017. http://dx.doi.org/10.18690/978-961-286-048-6.3.

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Wei-Kit, Danny Chin, Steven Lim, Pang Yean-Ling, and Wong Kam-Huei. "Application of Organosolv Pretreatment on Pennisetum Purpureum for Lignin Removal and Cellulose Recovery." In ICBBE 2017: 2017 4th International Conference on Biomedical and Bioinformatics Engineering. New York, NY, USA: ACM, 2017. http://dx.doi.org/10.1145/3168776.3168781.

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Barrera Arellano, Daniel, and Juliana Annes Erbolato. "SISTEMAS ORGANOGEL-AMIDO E SUAS EMULSÕES: CARACTERÍSTICAS REOLÓGICAS E ESTABILIDADE." In XXIII Congresso de Iniciação Científica da Unicamp. Campinas - SP, Brazil: Galoá, 2015. http://dx.doi.org/10.19146/pibic-2015-37445.

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"Cement-Based Composites Reinforced with Nanofibrillated Cellulose from Bamboo Organossolv Pulp." In Non-Conventional Materials and Technologies. Materials Research Forum LLC, 2018. http://dx.doi.org/10.21741/9781945291838-12.

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Permatasari, Puspita Rahayu, Imam Prasetyo, and Teguh Ariyanto. "Synthesis of nanoporous carbon from mangosteen peel lignin extracted by using organosolv and soda processes." In THE 11TH REGIONAL CONFERENCE ON CHEMICAL ENGINEERING (RCChE 2018). Author(s), 2019. http://dx.doi.org/10.1063/1.5095029.

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