Relevant bibliographies by topics / Carbon dioxide

Contents

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

Academic literature on the topic 'Carbon dioxide'

Author: Grafiati
Published: 4 June 2021
Last updated: 30 November 2024

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Journal articles on the topic "Carbon dioxide"

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Zolotareva, O. K. "BIOCATALYTIC CARBON DIOXIDE CAPTURE PROMOTED BY CARBONIC ANHYDRASE." Biotechnologia Acta 16, no. 5 (October 31, 2023): 5–21. http://dx.doi.org/10.15407/biotech16.05.005.

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The rapid and steady increase in the concentration of CO2, the most abundant greenhouse gas in the atmosphere, leads to extreme weather and climate events. Due to the burning of fossil fuels (oil, coal and natural gas), the concentration of CO2 in the air has been increasing in recent decades by more than 2 ppm per year, and in the last year alone - by 3.29 ppm. To prevent the "worst" scenarios of climate change, immediate and significant reductions in CO2 emissions through carbon management are needed. Aim. Analysis of the current state of research and prospects for the use of carbonic anhydrase in environmental decarbonization programs. Results. Carbonic anhydrase (CA) is an enzyme that accelerates the exchange of CO2 and HCO3 in solution by a factor of 104 to 106. To date, 7 types of CAs have been identified in different organisms. CA is required to provide a rapid supply of CO2 and HCO3 for various metabolic pathways in the body, explaining its multiple independent origins during evolution. Enzymes isolated from bacteria and mammalian tissues have been tested in CO2 sequestration projects using carbonic anhydrase (CA). The most studied is one of the isoforms of human KAz - hCAII - the most active natural enzyme. Its drawbacks have been instability over time, high sensitivity to temperature, low tolerance to contaminants such as sulphur compounds and the impossibility of reuse. Molecular modelling and enzyme immobilisation methods were used to overcome these limitations. Immobilisation was shown to provide greater thermal and storage stability and increased reusability. Conclusions. Capturing carbon dioxide using carbonic anhydrase (CA) is one of the most cost-effective methods to mitigate global warming, the development of which requires significant efforts to improve the stability and thermal stability of CAs.
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Pimpare, Dr Meena M. "Correlation between End-Tidal Carbon Dioxide Pressure and Arterial Carbon Dioxide Partial Pressure in Patients Undergoing Craniotomy." Journal of Medical Science And clinical Research 05, no. 03 (March 7, 2017): 18525–33. http://dx.doi.org/10.18535/jmscr/v5i3.43.

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NAKAGAWA, Kameichiro. "Compacting Carbon Dioxide : Carbon Dioxide Geological Storage." Journal of the Society of Mechanical Engineers 113, no. 1099 (2010): 412–13. http://dx.doi.org/10.1299/jsmemag.113.1099_412.

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S, Damdinsuren, and Ariuntuya N. "Changes in the Concentration of Carbon Dioxide in the Air." Физик сэтгүүл 23, no. 455 (March 15, 2022): 1–4. http://dx.doi.org/10.22353/physics.v23i455.758.

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We are measuring the diurnal and seasonal changes in the concentration of carbon dioxidein the air of different natural zones of Mongolia from 2009. The carbon dioxide in airdecreased in the daytime and increased in the nighttime during the vegetation period. Thechanges in the concentration of carbon dioxide in the air were high in vegetation period, insteppe and in rainy summer. It was concluded and confirmed that the changes in theconcentration of carbon dioxide in the air controlled by the balance between thephotosynthetic uptake and respiratory emission of carbon dioxide.
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&NA;. "Carbon dioxide." Reactions Weekly &NA;, no. 1386 (January 2012): 14. http://dx.doi.org/10.2165/00128415-201213860-00046.

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&NA;. "Carbon dioxide." Reactions Weekly &NA;, no. 1311 (July 2010): 18. http://dx.doi.org/10.2165/00128415-201013110-00061.

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&NA;. "Carbon dioxide." Reactions Weekly &NA;, no. 1342 (March 2011): 11. http://dx.doi.org/10.2165/00128415-201113420-00036.

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&NA;. "Carbon dioxide." Reactions Weekly &NA;, no. 1347 (April 2011): 15–16. http://dx.doi.org/10.2165/00128415-201113470-00044.

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Benarie, Michel. "Carbon dioxide." Science of The Total Environment 41, no. 2 (February 1985): 199–201. http://dx.doi.org/10.1016/0048-9697(85)90193-7.

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Günel, Gökçe. "What Is Carbon Dioxide? When Is Carbon Dioxide?" PoLAR: Political and Legal Anthropology Review 39, no. 1 (May 2016): 33–45. http://dx.doi.org/10.1111/plar.12129.

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Dissertations / Theses on the topic "Carbon dioxide"

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Ferrufino, Gretta Larisa Aurora Arce [UNESP]. "Uma modelagem de sequestro e armazenamento de dióxido de carbono atmosférico." Universidade Estadual Paulista (UNESP), 2008. http://hdl.handle.net/11449/99319.

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
O dióxido de carbono (CO2) é um importante gás de efeito estufa. No entanto, um aumento gradual ameaça substancialmente o clima. Um dos principais desafios do planejamento ambiental é identificar um modelo que vincule todos os fatores do ciclo de carbono, ou seja, oceano – ecossistema terrestre – emissão antropogênica – atmosfera. Princípios básicos de Termodinâmica podem ser aplicados em uma modelagem estatística com bases em séries históricas para obter concentrações de CO2 na atmosfera, possibilitando a construção de cenários para uma melhor tomada de decisões. Por este motivo, foi desenvolvido no trabalho um modelo que interliga todos os fatores do ciclo de carbono, focalizando em quatro zonas térmicas ou climáticas (Boreal, Temperada, Tropical, Polar), para cálculos de armazenamento de CO2 atmosférico. Os resultados mostram que no ano 2100 se atingirá uma concentração de CO2 quatro vezes maior do que antes do período pré-industrial. A zona temperada emite quase a metade de dióxido de carbono à atmosfera na atualidade; para o ano 2100, essa emissão aumentará a quinze vezes mais que a zona tropical. A China será responsável em uma proporção de vinte quatro a onze com relação aos Estados Unidos. A estabilização das concentrações de CO2 na atmosfera será obtida quando as emissões de dióxido de carbono antropogênico tiverem uma diminuição de mais do que trinta e quatro por cento para o ano 2100 na zona temperada.
Carbon dioxide (CO2) is the most important greenhouse gas. A gradual increase on its atmospheric concentration threatens significantly the climate. One of the main challenges of environment planning is to identify a model that connects all factors that determine the carbon cycle, that is, ocean – terrestrial ecosystem – anthropogenic emissions – atmosphere. Basic thermodynamic principles can be applied in a statistical modeling with historic time series to obtain atmospheric CO2 concentration, creating the possibility of construction of scenarios that will help decision making. A model that links all carbon cycle factors was developed in this dissertation work, focusing in four thermal of climatic zones (Boreal, Temperate, Tropical, and Polar) for calculations of atmospheric CO2 storage. Results show that in 2100, the atmospheric CO2 concentration will reach a value four times higher than that of the pre-industrial period. The temperate zone already emits almost half of the carbon dioxide to the atmosphere; by 2100, this emission will increase 15 times more than that corresponding to the tropical zone. China will be responsible for emissions in a proportion of 24 to 11 in comparison to that of the United States. Stabilization of CO2 concentrations in the atmosphere will be obtained when the anthropogenic carbon dioxide emissions attain a decrease of at least 34% in 2100 in the temperate zone.
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Ferrufino, Gretta Larisa Aurora Arce. "Uma modelagem de sequestro e armazenamento de dióxido de carbono atmosférico /." Guaratinguetá : [s.n.], 2009. http://hdl.handle.net/11449/99319.

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Resumo: O dióxido de carbono (CO2) é um importante gás de efeito estufa. No entanto, um aumento gradual ameaça substancialmente o clima. Um dos principais desafios do planejamento ambiental é identificar um modelo que vincule todos os fatores do ciclo de carbono, ou seja, oceano - ecossistema terrestre - emissão antropogênica - atmosfera. Princípios básicos de Termodinâmica podem ser aplicados em uma modelagem estatística com bases em séries históricas para obter concentrações de CO2 na atmosfera, possibilitando a construção de cenários para uma melhor tomada de decisões. Por este motivo, foi desenvolvido no trabalho um modelo que interliga todos os fatores do ciclo de carbono, focalizando em quatro zonas térmicas ou climáticas (Boreal, Temperada, Tropical, Polar), para cálculos de armazenamento de CO2 atmosférico. Os resultados mostram que no ano 2100 se atingirá uma concentração de CO2 quatro vezes maior do que antes do período pré-industrial. A zona temperada emite quase a metade de dióxido de carbono à atmosfera na atualidade; para o ano 2100, essa emissão aumentará a quinze vezes mais que a zona tropical. A China será responsável em uma proporção de vinte quatro a onze com relação aos Estados Unidos. A estabilização das concentrações de CO2 na atmosfera será obtida quando as emissões de dióxido de carbono antropogênico tiverem uma diminuição de mais do que trinta e quatro por cento para o ano 2100 na zona temperada.
Abstract: Carbon dioxide (CO2) is the most important greenhouse gas. A gradual increase on its atmospheric concentration threatens significantly the climate. One of the main challenges of environment planning is to identify a model that connects all factors that determine the carbon cycle, that is, ocean - terrestrial ecosystem - anthropogenic emissions - atmosphere. Basic thermodynamic principles can be applied in a statistical modeling with historic time series to obtain atmospheric CO2 concentration, creating the possibility of construction of scenarios that will help decision making. A model that links all carbon cycle factors was developed in this dissertation work, focusing in four thermal of climatic zones (Boreal, Temperate, Tropical, and Polar) for calculations of atmospheric CO2 storage. Results show that in 2100, the atmospheric CO2 concentration will reach a value four times higher than that of the pre-industrial period. The temperate zone already emits almost half of the carbon dioxide to the atmosphere; by 2100, this emission will increase 15 times more than that corresponding to the tropical zone. China will be responsible for emissions in a proportion of 24 to 11 in comparison to that of the United States. Stabilization of CO2 concentrations in the atmosphere will be obtained when the anthropogenic carbon dioxide emissions attain a decrease of at least 34% in 2100 in the temperate zone.
Orientador: João Andrade de Carvalho Junior
Coorientador: Luiz Fernando Costa Nascimento
Banca: José Antonio Perrella Balestieri
Banca: Maria Paulete Pereira Martins Jorge
Mestre
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Jankhah, Sepideh. "Reformage de l'éthanol au dioxyde de carbone Ethanol reforming with carbon dioxide /." [S.l. : s.n.], 2007.

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Sirokman, Gergely. "(N-heterocyclic-carbene)Copper(I)-catalyzed carbon-carbon bond formation using carbon dioxide." Thesis, Massachusetts Institute of Technology, 2007. http://hdl.handle.net/1721.1/39584.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2007.
Vita.
Includes bibliographical references.
This thesis presents work towards the development of a new catalytic C-C bond forming reaction. Alkynes and olefins insert into [(IPr)CuH]2 (IPr = N,N-bis-(2,6-diisopropylphenyl)-1,3-imidazol-2-ylidene) to give copper vinyl and copper alkyl complexes. These copper complexes insert CO2 into the Cu-C bond to form copper acrylate and copper carboxylate complexes. Acrylic and carboxylic acids can be isolated by hydrolysis. A catalytic cycle based on (IPr)copper(I) was developed. Alkynes undergo reductive carboxylation to give acrylic acids in moderate yields. Unexpected interactions between several components of the catalytic system led to a number of side reaction, most importantly between [(IPr)CuH]2 and the product silyl acrylate. The use of silylcarbonate salts to desylilate the product enhanced yield. In addition, silylcarbonates can also serve as a source of CO2.
by Gergely Sirokman.
Ph.D.
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Carney, Kevin. "Supercritical Carbon Dioxide Extraction." DigitalCommons@CalPoly, 2017. https://digitalcommons.calpoly.edu/theses/1755.

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The objective of this thesis is to explore the properties of supercritical carbon dioxide (CO2). In addition, the feasibility of building a small-scale low cost system will be explained. A supercritical fluid is a fluid which exhibits properties between liquid and gas with liquid like densities and viscosities similar to a gas. Since the discovery of supercritical fluids in 1822, the use of supercritical fluids, specifically supercritical CO2, has grown in popularity. The application of supercritical CO2 has continued to grow in industrial applications since the 1970’s. Supercritical CO2’s has many beneficial properties as a “green” solvent. Supercritical CO2 as a solvent is able to be implemented in a wide range of applications from aerospace, microchip manufacturing, food production, biomedical, pharmaceutical, dry-cleaning, and many more. This thesis project included designing, building and testing a supercritical CO2 extraction apparatus that examines the use of supercritical CO2 as a solvent in the extraction process of decaffeinating coffee. Due to the fact that supercritical CO2 requires high pressure operating conditions, the apparatus design is important not only for function but also for safety. In the description portion of this paper, design considerations related to each component’s function and their specific roles in the overall system are clearly stated. Furthermore, the build process is outlined along with the overall step-by-step operation of the apparatus. Different methods of data measurements are taken while the system is running, in order to interpret the apparatus’ overall functionality. Through the exploration of this experimental data, the results were compared between different operating parameters. In order to determine the feasibility of the supercritical apparatus, the devise was tested by applying the supercritical CO2 as a solvent for the extraction of caffeine from coffee beans. Analysis of the analytical data recorded from experimental testing confirms that the apparatus produced supercritical CO2. After testing specific operating conditions, it is proven that the supercritical CO2 is able to function as a “green” solvent in this small-scale system. The experimental results from these analytical runs are compared with theoretical maximums in order to determine the efficiency of the devise. Lastly, the paper presents an overview including lessons learned from the design process and from the information gathered. Data from experimental testing is interpreted and the system design is reevaluated with suggestions for future improvements.
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Ferrufino, Gretta Larisa Aurora Arce [UNESP]. "Análise de propostas de sequestro mineral de carbono para usinas termoelétricas no Brasil." Universidade Estadual Paulista (UNESP), 2012. http://hdl.handle.net/11449/106453.

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Acordos internacionais sobre o aquecimento global têm identificado a urgente necessidade por uma tecnologia que capture e sequestre carbono em grande escala para reduzir as emissões de dióxido de carbono (CO2) antrópico. O sequestro e captura do CO2 por carbonatação mineral (CCSM) é uma tecnologia que tem potencial para reduzir bilhões de toneladas de CO2 por ano. O principal foco deste trabalho foi avaliar o efeito ambiental do requerimento energético relacionada à produção de carbonatos utilizando os minerais silicatos, com a finalidade de sequestrar emissões de CO2 provenientes de usinas termelétricas no Brasil. Esta pesquisa foi realizada mediante o uso do LCA - Life Cycle Assessment (NBR 14040) identificando quatro subsistemas (processos de mineração, transporte do mineral, usina termelétrica e processos de carbonatação mineral) na produção de carbonatos. Consideraram-se dois processos de carbonatação mineral: mediante o ácido clorídrico (HCl) e sais de amônia (NH4HSO4) integrados a dois tipos de usinas termelétricas (carvão e gás natural), adotando quatro cenários nos quais foram avaliados o requerimento energético, emissões de CO2 e os custos envolvidos de cada um deles, as quais utilizaram a matéria prima com maior potencial de carbonatação (mineral silicato). O presente estudo foi estruturado visando responder os seguintes assuntos: (a) O melhor mineral silicato como matéria prima para processo de carbonatação mineral, (b) A quantidade de matéria prima para a sequestro de 1 tonelada de CO2, (c) O requerimento energético do processo de carbonatação mineral para sequestrar 1 tonelada de CO2, (d) A quantidade de CO2 evitada derivada da produção de carbonatos e (e) Comparação do resultado do LCA dos processos de carbonatação mineral considerados no estudo. Os resultados amostram...
International concerns over global warming have identified the urgent need for a technology to capture and sequester carbon in large-scale to reduce anthropic carbon dioxide (CO2) emissions. Carbon dioxide capture and sequestration by mineral carbonation (CCSM) is a technology that can potentially reduce billions of tonnes of CO2 per year. The main focus of this work was to evaluate the environmental effects of energy usage related to carbonate production using mineral silicates in order to sequester CO2 emissions from Brazilian power plants. This investigation was realized using a LCA - Life Cycle Assessment (ISO14040) identified 4 subsystems (mining process, mineral transport, power plant and mineral carbonation process) on carbonate production. Two mineral carbonation processes are considered: using chloride acid (HCl) and ammonium salts (NH4HSO4) applied to two types of power plants (coal and natural gas) with the best feedstock (mineral silicate) supporting four scenarios which evaluate energy requirement, CO2 emissions and costs. This work addresses the following import issues: a) the best mineral silicate used as feedstock for mineral carbonation process, b) the amount of this mineral silicate for sequestration 1 ton CO2, c) the energy requirements of mineral carbonate process to sequester 1 ton of CO2, d) the amount of CO2 avoided derived from carbonate production and e) comparison of LCA results of the two mineral carbonation process. The LCA results shows that the best feedstock to sequester CO2 emissions from power plants in Brazil is serpentinito located in Goiâs state, the mineral carbonation process using ammonium salts is a feasible option for the less energy requirement (0,75 kW/kgCO2SEQ). The amount of CO2 avoided was 0,578 tCO2AVOIDED/tCO2SEQ, this avoided CO2 emissions can be traded as carbon... (Complete abstract click electronic access below)
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Ferrufino, Gretta Larisa Aurora Arce. "Análise de propostas de sequestro mineral de carbono para usinas termoelétricas no Brasil /." Guaratinguetá, 2013. http://hdl.handle.net/11449/106453.

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Orientador: João Andrade de Carvalho
Banca: Jose Antonio Perella Balestieri
Banca: Maria Angelica Martins Costa
Banca: Turíbio Gomes Soares Neto
Banca: Christian Jeremi Coronado Rodriguez
Resumo: Acordos internacionais sobre o aquecimento global têm identificado a urgente necessidade por uma tecnologia que capture e sequestre carbono em grande escala para reduzir as emissões de dióxido de carbono (CO2) antrópico. O sequestro e captura do CO2 por carbonatação mineral (CCSM) é uma tecnologia que tem potencial para reduzir bilhões de toneladas de CO2 por ano. O principal foco deste trabalho foi avaliar o efeito ambiental do requerimento energético relacionada à produção de carbonatos utilizando os minerais silicatos, com a finalidade de sequestrar emissões de CO2 provenientes de usinas termelétricas no Brasil. Esta pesquisa foi realizada mediante o uso do LCA - Life Cycle Assessment (NBR 14040) identificando quatro subsistemas (processos de mineração, transporte do mineral, usina termelétrica e processos de carbonatação mineral) na produção de carbonatos. Consideraram-se dois processos de carbonatação mineral: mediante o ácido clorídrico (HCl) e sais de amônia (NH4HSO4) integrados a dois tipos de usinas termelétricas (carvão e gás natural), adotando quatro cenários nos quais foram avaliados o requerimento energético, emissões de CO2 e os custos envolvidos de cada um deles, as quais utilizaram a matéria prima com maior potencial de carbonatação (mineral silicato). O presente estudo foi estruturado visando responder os seguintes assuntos: (a) O melhor mineral silicato como matéria prima para processo de carbonatação mineral, (b) A quantidade de matéria prima para a sequestro de 1 tonelada de CO2, (c) O requerimento energético do processo de carbonatação mineral para sequestrar 1 tonelada de CO2, (d) A quantidade de CO2 evitada derivada da produção de carbonatos e (e) Comparação do resultado do LCA dos processos de carbonatação mineral considerados no estudo. Os resultados amostram... (Resumo completo, clicar acesso eletrônico abaixo)
Abstract: International concerns over global warming have identified the urgent need for a technology to capture and sequester carbon in large-scale to reduce anthropic carbon dioxide (CO2) emissions. Carbon dioxide capture and sequestration by mineral carbonation (CCSM) is a technology that can potentially reduce billions of tonnes of CO2 per year. The main focus of this work was to evaluate the environmental effects of energy usage related to carbonate production using mineral silicates in order to sequester CO2 emissions from Brazilian power plants. This investigation was realized using a LCA - Life Cycle Assessment (ISO14040) identified 4 subsystems (mining process, mineral transport, power plant and mineral carbonation process) on carbonate production. Two mineral carbonation processes are considered: using chloride acid (HCl) and ammonium salts (NH4HSO4) applied to two types of power plants (coal and natural gas) with the best feedstock (mineral silicate) supporting four scenarios which evaluate energy requirement, CO2 emissions and costs. This work addresses the following import issues: a) the best mineral silicate used as feedstock for mineral carbonation process, b) the amount of this mineral silicate for sequestration 1 ton CO2, c) the energy requirements of mineral carbonate process to sequester 1 ton of CO2, d) the amount of CO2 avoided derived from carbonate production and e) comparison of LCA results of the two mineral carbonation process. The LCA results shows that the best feedstock to sequester CO2 emissions from power plants in Brazil is serpentinito located in Goiâs state, the mineral carbonation process using ammonium salts is a feasible option for the less energy requirement (0,75 kW/kgCO2SEQ). The amount of CO2 avoided was 0,578 tCO2AVOIDED/tCO2SEQ, this avoided CO2 emissions can be traded as carbon... (Complete abstract click electronic access below)
Doutor
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Marszewska, Jowita E. "Development of microporosity in carbons for carbon dioxide adsorption." Kent State University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=kent1492043634249216.

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Bagga, Rajinder S. "Biological sequestration of carbon dioxide." Ohio : Ohio University, 2000. http://www.ohiolink.edu/etd/view.cgi?ohiou1171386594.

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Sawalha, Samer. "Carbon Dioxide in Supermarket Refrigeration." Doctoral thesis, Stockholm : Energiteknik, Energy Technology, Kungliga Tekniska högskolan, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4753.

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Books on the topic "Carbon dioxide"

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Gopalan, Aravamudan S., Chien M. Wai, and Hollie K. Jacobs, eds. Supercritical Carbon Dioxide. Washington, DC: American Chemical Society, 2003. http://dx.doi.org/10.1021/bk-2003-0860.

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Robert, Marc, Cyrille Costentin, and Kim Daasbjerg, eds. Carbon Dioxide Electrochemistry. Cambridge: Royal Society of Chemistry, 2020. http://dx.doi.org/10.1039/9781788015844.

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Centi, Gabriele, and Siglinda Perathoner, eds. Green Carbon Dioxide. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118831922.

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Stan, Cornel. Energy versus Carbon Dioxide. Berlin, Heidelberg: Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-64162-0.

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Hashimoto, Koji. Global Carbon Dioxide Recycling. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-8584-1.

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Lu, Xiao-Bing, ed. Carbon Dioxide and Organometallics. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-22078-9.

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Aresta, Michele, and Angela Dibenedetto. The Carbon Dioxide Revolution. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-59061-1.

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Balaban, Murat O., and Giovanna Ferrentino, eds. Dense Phase Carbon Dioxide. Oxford, UK: Wiley-Blackwell, 2012. http://dx.doi.org/10.1002/9781118243350.

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Balaban, Murat O., and Giovanna Ferrentino. Dense phase carbon dioxide. Hoboken, N.J: Wiley-Blackwell, 2012.

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Schütze, Michael, Bernd Isecke, and Roman Bender. Corrosion protection against carbon dioxide. Frankfurt: DECHEMA, 2011.

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Book chapters on the topic "Carbon dioxide"

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Bährle-Rapp, Marina. "Carbon Dioxide." In Springer Lexikon Kosmetik und Körperpflege, 90. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1661.

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McCollom, Thomas. "Carbon Dioxide." In Encyclopedia of Astrobiology, 239–40. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_1737.

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Gooch, Jan W. "Carbon Dioxide." In Encyclopedic Dictionary of Polymers, 116. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1927.

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Price, Debra J. "Carbon Dioxide." In Hamilton & Hardy's Industrial Toxicology, 305–8. Hoboken, New Jersey: John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781118834015.ch42.

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Hay, William W. "Carbon Dioxide." In Experimenting on a Small Planet, 474–504. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-27404-1_21.

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McCollom, Thomas. "Carbon Dioxide." In Encyclopedia of Astrobiology, 365–66. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_1737.

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Hay, William W. "Carbon Dioxide." In Experimenting on a Small Planet, 620–71. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-28560-8_20.

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Bauman, Yoram, and Grady Klein. "Carbon Dioxide." In The Cartoon Introduction to Climate Change, 39–50. Washington, DC: Island Press/Center for Resource Economics, 2014. http://dx.doi.org/10.5822/978-1-61091-570-0_4.

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Hess-Kosa, Kathleen. "Carbon Dioxide." In Indoor Air Quality, 177–84. Third edition. | Boca Raton : CRC Press/Taylor & Francis, 2019.: CRC Press, 2018. http://dx.doi.org/10.1201/9781315098180-10.

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Willey, Neil. "Carbon Dioxide." In Environmental Plant Physiology, 51–76. New York, NY : Garland Science, 2016.: Garland Science, 2018. http://dx.doi.org/10.1201/9781317206231-3.

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Conference papers on the topic "Carbon dioxide"

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De Figueiredo, Mark, Lisa Bacanskas, and Michael Kolian. "Greenhouse Gas Reporting for Geologic Sequestration of Carbon Dioxide." In Carbon Management Technology Conference. Carbon Management Technology Conference, 2012. http://dx.doi.org/10.7122/151426-ms.

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Lau, Hon Chung, Chaobin Zhao, and Samuel W. Lau. "Coalbed Methane Recovery By Injection of Hot Carbon Dioxide." In Carbon Management Technology Conference. Carbon Management Technology Conference, 2017. http://dx.doi.org/10.7122/485492-ms.

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Wang, Shuoshi, Mohannad Kadhum, Qingwang Yuan, Bor-Jier Shiau, and Jeffrey H. Harwell. "Carbon Dioxide in Situ Generation for Enhanced Oil Recovery." In Carbon Management Technology Conference. Carbon Management Technology Conference, 2017. http://dx.doi.org/10.7122/486365-ms.

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Coelho, Raphael, Maria Barrufet, and Berna Hascakir. "Effect of Impurities in Carbon Dioxide Stream on Phase Behavior for Geological Storage of Carbon Dioxide in Low API Gravity Oil Reservoirs." In Carbon Management Technology Conference. Carbon Management Technology Conference, 2015. http://dx.doi.org/10.7122/439524-ms.

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Ibrahim, Ahmed Abdullah. "Carbon Dioxide and Carbon Monoxide Level Detector." In 2018 21st International Conference of Computer and Information Technology (ICCIT). IEEE, 2018. http://dx.doi.org/10.1109/iccitechn.2018.8631933.

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Wattana, P., A. Thivasasith, W. Nunthakitgoson, C. Rodaum, and C. Wattanakit. "Carbon Dioxide Conversion To Advanced Carbon Nanotubes." In ADIPEC. SPE, 2024. http://dx.doi.org/10.2118/222792-ms.

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Abstract The conversion of CO2 into valuable substances is a topic of great interest for decarbonization. Among them, the CO2 conversion to advanced materials such as carbon nanotubes (CNTs) has emerged as promising CO2 utilization. In this work, we have successfully developed catalysts and process to convert CO2 to CNTs. We developed catalysts by loading active transition metals on to hierarchical zeolite for CNT synthesis using CO2 as raw material. The synthesis of CNTs from CO2 over the developed catalysts was carried out via a chemical vapor deposition (CVD) process. The quantity and quality of the resulting carbon nanotubes were determined using thermogravimetric analysis (TGA), scanning electron microscope (SEM), transmission electron microscopy (TEM), and Raman spectroscopy. The synthesized CNTs were also evaluated for their current response using cyclic voltammetry (V vs. Ag/AgCl) method. By optimizing metal type, metal loading, zeolite topologies and pore structures (hierarchically porous or conventionally microporous), we successfully converted CO2 to CNTs over the metal-loaded hierarchical zeolite catalysts. The CNTs produced using the 25wt.% Fe on hierarchical FAU zeolite provided the most promising result with a high CNTs yield of 15.4%, an average CNTs diameter size of 23.1 nm, and ID/IG ratio of 0.56 indicating high quality CNTs. The synthesized CNTs were tested and exhibited higher current response compared to commercial CNTs. This enhanced performance highlights the significant contribution of the small diameter and superior quality of our synthesized pure CNT. Transition metals play a crucial role as catalysts in the decomposition of CO2 during the CNTs synthesis. Moreover, well-distribution of metal nanoparticles on the hierarchical zeolite contributes to enhanced catalytic activity, consequently resulting in more favorable CNTs synthesis outcomes. This work demonstrates conversion of CO2 towards highly conductive CNTs-based materials, which have many potential applications including energy storages, sensors, electronic circuits, etc.
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Hovorka, Susan. "Monitoring CO2 EOR Projects To Document Storage Permanence." In ACI’s 4th Carbon Dioxide Utilization Conference San Antonio, TX February 2015. US DOE, 2015. http://dx.doi.org/10.2172/1749868.

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Tsui, K. H. "Room temperature carbon dioxide lasers." In International Conference on Optoelectronic Science and Engineering '90. SPIE, 1990. http://dx.doi.org/10.1117/12.2294749.

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Blunt, M., R. Qi, and T. LaForce. "Design of carbon dioxide storage." In BHS 3rd International Conference. British Hydrological Society, 2010. http://dx.doi.org/10.7558/bhs.2010.ic43.

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Kucerovsky. "Computer controlled carbon dioxide laser." In Proceedings of Canadian Conference on Electrical and Computer Engineering CCECE-94. IEEE, 1994. http://dx.doi.org/10.1109/ccece.1994.405765.

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Reports on the topic "Carbon dioxide"

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Skone, Timothy J. Carbon Dioxide Dehydration. Office of Scientific and Technical Information (OSTI), November 2012. http://dx.doi.org/10.2172/1509004.

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Martin, Olga. Carbon Dioxide Decomposition. Office of Scientific and Technical Information (OSTI), October 2012. http://dx.doi.org/10.2172/1054236.

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Trabalka, J. Atmospheric carbon dioxide and the global carbon cycle. Office of Scientific and Technical Information (OSTI), December 1985. http://dx.doi.org/10.2172/6048470.

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Kennel, Elliot, and Robert Statnik. Carbon Dioxide Utilization for Plasma Nanosynthesis of Carbon. Office of Scientific and Technical Information (OSTI), April 2020. http://dx.doi.org/10.2172/1615509.

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Gerth, Wayne A. Chamber Carbon Dioxide and Ventilation. Fort Belvoir, VA: Defense Technical Information Center, November 2004. http://dx.doi.org/10.21236/ada442939.

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Wagonner, R. C. Carbon Dioxide for pH Control. Office of Scientific and Technical Information (OSTI), August 2001. http://dx.doi.org/10.2172/785010.

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K.A.M. Gasem, Jr R.L. Robinson, and L.R. Radovic. SEQUESTERING CARBON DIOXIDE IN COALBEDS. Office of Scientific and Technical Information (OSTI), June 2001. http://dx.doi.org/10.2172/812557.

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K.A.M. Gasem, Jr R.L. Robinson, and L.R. Radovic. SEQUESTERING CARBON DIOXIDE IN COALBEDS. Office of Scientific and Technical Information (OSTI), June 2001. http://dx.doi.org/10.2172/812558.

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K.A.M. Gasem, Jr R.L. Robinson, and L.R. Radovic. SEQUESTERING CARBON DIOXIDE IN COALBEDS. Office of Scientific and Technical Information (OSTI), December 2001. http://dx.doi.org/10.2172/812559.

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K.A.M. Gasem, Jr R.L. Robinson, and L.R. Radovic. SEQUESTERING CARBON DIOXIDE IN COALBEDS. Office of Scientific and Technical Information (OSTI), March 2003. http://dx.doi.org/10.2172/812560.

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