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  • Fonte: Green Chemistry. Unidade: IQ

    Assuntos: QUÍMICA VERDE, ELETROANÁLISE

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      BARROS, Tayná Silva Bernardino et al. Beyond bubbles: greener flow-based electroanalysis by an air-driven carrier. Green Chemistry, v. 27, n. 37, p. 11354-11364, 2025Tradução . . Disponível em: https://dx.doi.org/10.1039/d5gc02382c. Acesso em: 03 dez. 2025.
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      Barros, T. S. B., Osorio, E. de L., Carvalho, C. T. de, Rodrigues, R., Angnes, L., & Trindade, M. A. G. (2025). Beyond bubbles: greener flow-based electroanalysis by an air-driven carrier. Green Chemistry, 27( 37), 11354-11364. doi:10.1039/d5gc02382c
    • NLM

      Barros TSB, Osorio E de L, Carvalho CT de, Rodrigues R, Angnes L, Trindade MAG. Beyond bubbles: greener flow-based electroanalysis by an air-driven carrier [Internet]. Green Chemistry. 2025 ; 27( 37): 11354-11364.[citado 2025 dez. 03 ] Available from: https://dx.doi.org/10.1039/d5gc02382c
    • Vancouver

      Barros TSB, Osorio E de L, Carvalho CT de, Rodrigues R, Angnes L, Trindade MAG. Beyond bubbles: greener flow-based electroanalysis by an air-driven carrier [Internet]. Green Chemistry. 2025 ; 27( 37): 11354-11364.[citado 2025 dez. 03 ] Available from: https://dx.doi.org/10.1039/d5gc02382c
  • Fonte: Green Chemistry. Unidade: IQSC

    Assuntos: QUÍMICA AMBIENTAL, SUSTENTABILIDADE, POLIMERIZAÇÃO, DENDÊ

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      ALARCON, Rafael Turra et al. Greener preparation of a flexible material based on macaw palm oil derivatives and CO2. Green Chemistry, v. 26, p. 3261-3270, 2024Tradução . . Disponível em: https://doi.org/10.1039/D3GC03933A. Acesso em: 03 dez. 2025.
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      Alarcon, R. T., Gaglieri, C., Bannach, G., & Cavalheiro, E. T. G. (2024). Greener preparation of a flexible material based on macaw palm oil derivatives and CO2. Green Chemistry, 26, 3261-3270. doi:10.1039/d3gc03933a
    • NLM

      Alarcon RT, Gaglieri C, Bannach G, Cavalheiro ETG. Greener preparation of a flexible material based on macaw palm oil derivatives and CO2 [Internet]. Green Chemistry. 2024 ; 26 3261-3270.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/D3GC03933A
    • Vancouver

      Alarcon RT, Gaglieri C, Bannach G, Cavalheiro ETG. Greener preparation of a flexible material based on macaw palm oil derivatives and CO2 [Internet]. Green Chemistry. 2024 ; 26 3261-3270.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/D3GC03933A
  • Fonte: Green Chemistry. Unidade: IQ

    Assuntos: COMBUSTÍVEIS, SILVICULTURA

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      LEBEDEVA, Daria et al. Sustainable aviation fuel from prehydrolysis liquors. Green Chemistry, v. 26, n. 12, p. 7258-7267, 2024Tradução . . Disponível em: https://dx.doi.org/10.1039/d4gc01257g. Acesso em: 03 dez. 2025.
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      Lebedeva, D., Schick, L. W., Cracco, D., Sangsuwan, W., Ona, G. C., Silva, D. O., et al. (2024). Sustainable aviation fuel from prehydrolysis liquors. Green Chemistry, 26( 12), 7258-7267. doi:10.1039/d4gc01257g
    • NLM

      Lebedeva D, Schick LW, Cracco D, Sangsuwan W, Ona GC, Silva DO, Marson A, Grape ES, Inge AK, Rossi LM, Subbotina E, Manzardo A, Samec JSM. Sustainable aviation fuel from prehydrolysis liquors [Internet]. Green Chemistry. 2024 ; 26( 12): 7258-7267.[citado 2025 dez. 03 ] Available from: https://dx.doi.org/10.1039/d4gc01257g
    • Vancouver

      Lebedeva D, Schick LW, Cracco D, Sangsuwan W, Ona GC, Silva DO, Marson A, Grape ES, Inge AK, Rossi LM, Subbotina E, Manzardo A, Samec JSM. Sustainable aviation fuel from prehydrolysis liquors [Internet]. Green Chemistry. 2024 ; 26( 12): 7258-7267.[citado 2025 dez. 03 ] Available from: https://dx.doi.org/10.1039/d4gc01257g
  • Fonte: Green Chemistry. Unidade: IQ

    Assuntos: DESENVOLVIMENTO SUSTENTÁVEL, ELETROQUÍMICA

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      CRAPNELL, Robert D et al. Utilising bio-based plasticiser castor oil and recycled PLA for the production of conductive additive manufacturing feedstock and detection of bisphenol A. Green Chemistry, v. 25, p. 5591-5600, 2023Tradução . . Disponível em: https://doi.org/10.1039/d3gc01700a. Acesso em: 03 dez. 2025.
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      Crapnell, R. D., Arantes, I. V. S., Whittingham, M. J., Sigley, E., Kalinke, C., Janegitz, B. C., et al. (2023). Utilising bio-based plasticiser castor oil and recycled PLA for the production of conductive additive manufacturing feedstock and detection of bisphenol A. Green Chemistry, 25, 5591-5600. doi:10.1039/d3gc01700a
    • NLM

      Crapnell RD, Arantes IVS, Whittingham MJ, Sigley E, Kalinke C, Janegitz BC, Bonacin JA, Paixão TRLC da, Banks CE. Utilising bio-based plasticiser castor oil and recycled PLA for the production of conductive additive manufacturing feedstock and detection of bisphenol A [Internet]. Green Chemistry. 2023 ; 25 5591-5600.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/d3gc01700a
    • Vancouver

      Crapnell RD, Arantes IVS, Whittingham MJ, Sigley E, Kalinke C, Janegitz BC, Bonacin JA, Paixão TRLC da, Banks CE. Utilising bio-based plasticiser castor oil and recycled PLA for the production of conductive additive manufacturing feedstock and detection of bisphenol A [Internet]. Green Chemistry. 2023 ; 25 5591-5600.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/d3gc01700a
  • Fonte: Green Chemistry. Unidade: FCF

    Assuntos: LÍQUIDOS IÔNICOS, SOLVENTE

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      MUSSAGY, Cassamo U et al. Ionic liquids or eutectic solvents? Identifying the best solvents for the extraction of astaxanthin and β-carotene from Phaffia rhodozyma yeast and preparation of biodegradable films. Green Chemistry, v. 24, p. 118–123, 2022Tradução . . Disponível em: https://doi.org/10.1039/d1gc03521e. Acesso em: 03 dez. 2025.
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      Mussagy, C. U., Ebinuma, V. de C. S., Herculano, R. D., Coutinho, J. A. P., Pereira, J. F. B., & Pessoa Junior, A. (2022). Ionic liquids or eutectic solvents? Identifying the best solvents for the extraction of astaxanthin and β-carotene from Phaffia rhodozyma yeast and preparation of biodegradable films. Green Chemistry, 24, 118–123. doi:10.1039/d1gc03521e
    • NLM

      Mussagy CU, Ebinuma V de CS, Herculano RD, Coutinho JAP, Pereira JFB, Pessoa Junior A. Ionic liquids or eutectic solvents? Identifying the best solvents for the extraction of astaxanthin and β-carotene from Phaffia rhodozyma yeast and preparation of biodegradable films [Internet]. Green Chemistry. 2022 ; 24 118–123.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/d1gc03521e
    • Vancouver

      Mussagy CU, Ebinuma V de CS, Herculano RD, Coutinho JAP, Pereira JFB, Pessoa Junior A. Ionic liquids or eutectic solvents? Identifying the best solvents for the extraction of astaxanthin and β-carotene from Phaffia rhodozyma yeast and preparation of biodegradable films [Internet]. Green Chemistry. 2022 ; 24 118–123.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/d1gc03521e
  • Fonte: Green Chemistry. Unidade: IQ

    Assuntos: RESINAS, COMPOSTOS ORGÂNICOS, CATALISADORES

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      DIAS, Kevin de Aquino e PEREIRA JÚNIOR, Marcus Vinícius e ANDRADE, Leandro Helgueira. Benzoic acid resin (BAR): a heterogeneous redox organocatalyst for continuous flow synthesis of benzoquinones from β-O-4 lignin models. Green Chemistry, v. 23, p. 2308-2316 : + Supplementary materials ( S1-S32), 2021Tradução . . Disponível em: https://doi.org/10.1039/d0gc04231e. Acesso em: 03 dez. 2025.
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      Dias, K. de A., Pereira Júnior, M. V., & Andrade, L. H. (2021). Benzoic acid resin (BAR): a heterogeneous redox organocatalyst for continuous flow synthesis of benzoquinones from β-O-4 lignin models. Green Chemistry, 23, 2308-2316 : + Supplementary materials ( S1-S32). doi:10.1039/d0gc04231e
    • NLM

      Dias K de A, Pereira Júnior MV, Andrade LH. Benzoic acid resin (BAR): a heterogeneous redox organocatalyst for continuous flow synthesis of benzoquinones from β-O-4 lignin models [Internet]. Green Chemistry. 2021 ; 23 2308-2316 : + Supplementary materials ( S1-S32).[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/d0gc04231e
    • Vancouver

      Dias K de A, Pereira Júnior MV, Andrade LH. Benzoic acid resin (BAR): a heterogeneous redox organocatalyst for continuous flow synthesis of benzoquinones from β-O-4 lignin models [Internet]. Green Chemistry. 2021 ; 23 2308-2316 : + Supplementary materials ( S1-S32).[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/d0gc04231e
  • Fonte: Green Chemistry. Unidade: FCF

    Assuntos: ECOSSISTEMAS OCEÂNICOS, ECOSSISTEMAS AQUÁTICOS, QUÍMICA VERDE, SUSTENTABILIDADE

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      VERÍSSIMO, Nathalia Vieira et al. From green to blue economy: marine biorefineries for a sustainable ocean-based economy. Green Chemistry, v. 23, p. 9377–9400, 2021Tradução . . Disponível em: https://doi.org/10.1039/d1gc03191k. Acesso em: 03 dez. 2025.
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      Veríssimo, N. V., Mussagy, C. U., Oshiro, A. A., Mendonça, C. M. N., Ebinuma, V. de C. S., Pessoa Junior, A., et al. (2021). From green to blue economy: marine biorefineries for a sustainable ocean-based economy. Green Chemistry, 23, 9377–9400. doi:10.1039/d1gc03191k
    • NLM

      Veríssimo NV, Mussagy CU, Oshiro AA, Mendonça CMN, Ebinuma V de CS, Pessoa Junior A, Oliveira RP de S, Pereira JFB. From green to blue economy: marine biorefineries for a sustainable ocean-based economy [Internet]. Green Chemistry. 2021 ; 23 9377–9400.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/d1gc03191k
    • Vancouver

      Veríssimo NV, Mussagy CU, Oshiro AA, Mendonça CMN, Ebinuma V de CS, Pessoa Junior A, Oliveira RP de S, Pereira JFB. From green to blue economy: marine biorefineries for a sustainable ocean-based economy [Internet]. Green Chemistry. 2021 ; 23 9377–9400.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/d1gc03191k
  • Fonte: Green Chemistry. Unidade: IQ

    Assuntos: CATALISADORES, OURO, OXIDAÇÃO, BIOMASSA

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      FERRAZ, Camila Palombo et al. Enhancing the activity of gold supported catalysts by oxide coating: towards efficient oxidations. Green Chemistry, v. 23, p. 8453–8457, 2021Tradução . . Disponível em: https://doi.org/10.1039/d1gc02889h. Acesso em: 03 dez. 2025.
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      Ferraz, C. P., Jaén, S. N., Rossi, L. M., Dumeignil, F., Ghazzal, M. N., & Wojcieszak, R. (2021). Enhancing the activity of gold supported catalysts by oxide coating: towards efficient oxidations. Green Chemistry, 23, 8453–8457. doi:10.1039/d1gc02889h
    • NLM

      Ferraz CP, Jaén SN, Rossi LM, Dumeignil F, Ghazzal MN, Wojcieszak R. Enhancing the activity of gold supported catalysts by oxide coating: towards efficient oxidations [Internet]. Green Chemistry. 2021 ; 23 8453–8457.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/d1gc02889h
    • Vancouver

      Ferraz CP, Jaén SN, Rossi LM, Dumeignil F, Ghazzal MN, Wojcieszak R. Enhancing the activity of gold supported catalysts by oxide coating: towards efficient oxidations [Internet]. Green Chemistry. 2021 ; 23 8453–8457.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/d1gc02889h
  • Fonte: Green Chemistry. Unidade: FCF

    Assuntos: QUÍMICA VERDE, BIODISPONIBILIDADE

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      SANTOS, João Henrique Picado Madalena et al. Continuous separation of cytochrome-c PEGylated conjugates by fast centrifugal partition chromatography. Green Chemistry, v. 21, n. 20, p. 5501-5506, 2019Tradução . . Disponível em: https://doi.org/10.1039/c9gc01063g. Acesso em: 03 dez. 2025.
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      Santos, J. H. P. M., Ferreira, A. M., Almeida, M. R., Quinteiro, P. S. G. N., Dias, A. C. R. V., Coutinho, J. A. P., et al. (2019). Continuous separation of cytochrome-c PEGylated conjugates by fast centrifugal partition chromatography. Green Chemistry, 21( 20), 5501-5506. doi:10.1039/c9gc01063g
    • NLM

      Santos JHPM, Ferreira AM, Almeida MR, Quinteiro PSGN, Dias ACRV, Coutinho JAP, Freire MG, Rangel-Yagui C de O, Ventura SPM. Continuous separation of cytochrome-c PEGylated conjugates by fast centrifugal partition chromatography [Internet]. Green Chemistry. 2019 ; 21( 20): 5501-5506.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c9gc01063g
    • Vancouver

      Santos JHPM, Ferreira AM, Almeida MR, Quinteiro PSGN, Dias ACRV, Coutinho JAP, Freire MG, Rangel-Yagui C de O, Ventura SPM. Continuous separation of cytochrome-c PEGylated conjugates by fast centrifugal partition chromatography [Internet]. Green Chemistry. 2019 ; 21( 20): 5501-5506.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c9gc01063g
  • Fonte: Green Chemistry. Unidade: IFSC

    Assuntos: SUSTENTABILIDADE, IMPACTOS AMBIENTAIS, HERBICIDAS, AGRICULTURA

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      CARVALHO JUNIOR, Paulo S. et al. Highly water soluble agrichemicals by using engineered organic salts for reducing adverse environmental impacts. Green Chemistry, v. 21, n. 23, p. 6419-6429, 2019Tradução . . Disponível em: https://doi.org/10.1039/c9gc02439e. Acesso em: 03 dez. 2025.
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      Carvalho Junior, P. S., Guimarães, G. G. F., Diniz, L. F., Ellena, J., & Oliveira, C. R. (2019). Highly water soluble agrichemicals by using engineered organic salts for reducing adverse environmental impacts. Green Chemistry, 21( 23), 6419-6429. doi:10.1039/c9gc02439e
    • NLM

      Carvalho Junior PS, Guimarães GGF, Diniz LF, Ellena J, Oliveira CR. Highly water soluble agrichemicals by using engineered organic salts for reducing adverse environmental impacts [Internet]. Green Chemistry. 2019 ; 21( 23): 6419-6429.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c9gc02439e
    • Vancouver

      Carvalho Junior PS, Guimarães GGF, Diniz LF, Ellena J, Oliveira CR. Highly water soluble agrichemicals by using engineered organic salts for reducing adverse environmental impacts [Internet]. Green Chemistry. 2019 ; 21( 23): 6419-6429.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c9gc02439e
  • Fonte: Green Chemistry. Unidade: FZEA

    Assuntos: DIGESTÃO ANAERÓBIA, CARVÃO ATIVADO, OZÔNIO

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      SI, Buchun et al. Anaerobic conversion of the hydrothermal liquefaction aqueous phase: fate of organics and intensification with granule activated carbon/ozone pretreatment. Green Chemistry, v. 21, n. 6, p. 1305-1318, 2019Tradução . . Disponível em: https://doi.org/10.1039/C8GC02907E. Acesso em: 03 dez. 2025.
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      Si, B., Yang, L., Zhou, X., Watson, J., Tommaso, G., Chen, W. -T., et al. (2019). Anaerobic conversion of the hydrothermal liquefaction aqueous phase: fate of organics and intensification with granule activated carbon/ozone pretreatment. Green Chemistry, 21( 6), 1305-1318. doi:10.1039/C8GC02907E
    • NLM

      Si B, Yang L, Zhou X, Watson J, Tommaso G, Chen W-T, Liao Q, Duan N, Liu Z, Zhang Y. Anaerobic conversion of the hydrothermal liquefaction aqueous phase: fate of organics and intensification with granule activated carbon/ozone pretreatment [Internet]. Green Chemistry. 2019 ; 21( 6): 1305-1318.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/C8GC02907E
    • Vancouver

      Si B, Yang L, Zhou X, Watson J, Tommaso G, Chen W-T, Liao Q, Duan N, Liu Z, Zhang Y. Anaerobic conversion of the hydrothermal liquefaction aqueous phase: fate of organics and intensification with granule activated carbon/ozone pretreatment [Internet]. Green Chemistry. 2019 ; 21( 6): 1305-1318.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/C8GC02907E
  • Fonte: Green Chemistry. Unidade: IQSC

    Assuntos: QUÍMICA VERDE, BIOMASSA

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      SANTOS, Camila et al. Synthesis of long-chain polyols from the Claisen condensation of γ-valerolactone. Green Chemistry, v. 21, p. 6441-6450, 2019Tradução . . Disponível em: https://doi.org/10.1039/c9gc03343b. Acesso em: 03 dez. 2025.
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      Santos, C., Soares, C. C. dos S. P., Vieira, A. S., & Burtoloso, A. C. B. (2019). Synthesis of long-chain polyols from the Claisen condensation of γ-valerolactone. Green Chemistry, 21, 6441-6450. doi:10.1039/c9gc03343b
    • NLM

      Santos C, Soares CC dos SP, Vieira AS, Burtoloso ACB. Synthesis of long-chain polyols from the Claisen condensation of γ-valerolactone [Internet]. Green Chemistry. 2019 ; 21 6441-6450.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c9gc03343b
    • Vancouver

      Santos C, Soares CC dos SP, Vieira AS, Burtoloso ACB. Synthesis of long-chain polyols from the Claisen condensation of γ-valerolactone [Internet]. Green Chemistry. 2019 ; 21 6441-6450.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c9gc03343b
  • Fonte: Green Chemistry. Unidades: FCF, IQ

    Assuntos: PROTEÍNAS, QUÍMICA VERDE

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      SANTOS, João Henrique Picado Madalena et al. An integrated process combining the reaction and purification of PEGylated proteins. Green Chemistry, v. 21, n. 23, p. 6407-6418, 2019Tradução . . Disponível em: https://doi.org/10.1039/c9gc01459d. Acesso em: 03 dez. 2025.
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      Santos, J. H. P. M., Mendonça, C. M. N., Silva, A. R. P. da, Oliveira, R. P. de S., Pessoa Junior, A., Coutinho, J. M. da C. e A. P., et al. (2019). An integrated process combining the reaction and purification of PEGylated proteins. Green Chemistry, 21( 23), 6407-6418. doi:10.1039/c9gc01459d
    • NLM

      Santos JHPM, Mendonça CMN, Silva ARP da, Oliveira RP de S, Pessoa Junior A, Coutinho JM da C e AP, Ventura SPM, Rangel-Yagui C de O. An integrated process combining the reaction and purification of PEGylated proteins [Internet]. Green Chemistry. 2019 ; 21( 23): 6407-6418.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c9gc01459d
    • Vancouver

      Santos JHPM, Mendonça CMN, Silva ARP da, Oliveira RP de S, Pessoa Junior A, Coutinho JM da C e AP, Ventura SPM, Rangel-Yagui C de O. An integrated process combining the reaction and purification of PEGylated proteins [Internet]. Green Chemistry. 2019 ; 21( 23): 6407-6418.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c9gc01459d
  • Fonte: Green Chemistry. Unidade: IQSC

    Assuntos: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      GALLO, Rafael D. C e BURTOLOSO, Antonio Carlos Bender. Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds. Green Chemistry, v. 20, p. 4547-4556, 2018Tradução . . Disponível em: https://doi.org/10.1039/C8GC02574F. Acesso em: 03 dez. 2025.
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      Gallo, R. D. C., & Burtoloso, A. C. B. (2018). Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds. Green Chemistry, 20, 4547-4556. doi:10.1039/C8GC02574F
    • NLM

      Gallo RDC, Burtoloso ACB. Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds [Internet]. Green Chemistry. 2018 ;20 4547-4556.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/C8GC02574F
    • Vancouver

      Gallo RDC, Burtoloso ACB. Silica-supported HClO4 promotes catalytic solvent- and metal-free O-H insertion reactions with diazo compounds [Internet]. Green Chemistry. 2018 ;20 4547-4556.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/C8GC02574F
  • Fonte: Green Chemistry. Unidade: FCF

    Assuntos: PROTEÍNAS, EXTRAÇÃO DE LÍQUIDOS

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      SANTOS, João Henrique Picado Madalena et al. Multistep purification of cytochrome c PEGylated forms using polymer-based aqueous biphasic systems. Green Chemistry, v. 19, p. 5800-5808, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7gc02600e. Acesso em: 03 dez. 2025.
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      Santos, J. H. P. M., Carretero, G. P. B., Coutinho, J. A. P., Rangel-Yagui, C. de O., & Ventura, S. P. M. (2017). Multistep purification of cytochrome c PEGylated forms using polymer-based aqueous biphasic systems. Green Chemistry, 19, 5800-5808. doi:10.1039/c7gc02600e
    • NLM

      Santos JHPM, Carretero GPB, Coutinho JAP, Rangel-Yagui C de O, Ventura SPM. Multistep purification of cytochrome c PEGylated forms using polymer-based aqueous biphasic systems [Internet]. Green Chemistry. 2017 ; 19 5800-5808.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c7gc02600e
    • Vancouver

      Santos JHPM, Carretero GPB, Coutinho JAP, Rangel-Yagui C de O, Ventura SPM. Multistep purification of cytochrome c PEGylated forms using polymer-based aqueous biphasic systems [Internet]. Green Chemistry. 2017 ; 19 5800-5808.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c7gc02600e
  • Fonte: Green Chemistry. Unidade: IQ

    Assunto: NANOTECNOLOGIA

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      TOMA, Henrique Eisi. Magnetic nanohydrometallurgy: a nanotechnological approach to elemental sustainability. Green Chemistry, v. 17, n. 4, p. 2027-2041, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5gc00066a. Acesso em: 03 dez. 2025.
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      Toma, H. E. (2015). Magnetic nanohydrometallurgy: a nanotechnological approach to elemental sustainability. Green Chemistry, 17( 4), 2027-2041. doi:10.1039/c5gc00066a
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      Toma HE. Magnetic nanohydrometallurgy: a nanotechnological approach to elemental sustainability [Internet]. Green Chemistry. 2015 ; 17( 4): 2027-2041.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c5gc00066a
    • Vancouver

      Toma HE. Magnetic nanohydrometallurgy: a nanotechnological approach to elemental sustainability [Internet]. Green Chemistry. 2015 ; 17( 4): 2027-2041.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c5gc00066a
  • Fonte: Green Chemistry. Unidade: IQ

    Assuntos: NANOPARTÍCULAS, NANOTECNOLOGIA

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      ROSSI, Liane Marcia et al. Magnetic nanomaterials in catalysis: advanced catalysts for magnetic separation and beyond. Green Chemistry, v. 16, n. 6, p. 2906-2933, 2014Tradução . . Disponível em: https://doi.org/10.1039/c4gc00164h. Acesso em: 03 dez. 2025.
    • APA

      Rossi, L. M., Costa, N. de J. da S., Silva, F. P. da, & Wojcieszak, R. (2014). Magnetic nanomaterials in catalysis: advanced catalysts for magnetic separation and beyond. Green Chemistry, 16( 6), 2906-2933. doi:10.1039/c4gc00164h
    • NLM

      Rossi LM, Costa N de J da S, Silva FP da, Wojcieszak R. Magnetic nanomaterials in catalysis: advanced catalysts for magnetic separation and beyond [Internet]. Green Chemistry. 2014 ; 16( 6): 2906-2933.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c4gc00164h
    • Vancouver

      Rossi LM, Costa N de J da S, Silva FP da, Wojcieszak R. Magnetic nanomaterials in catalysis: advanced catalysts for magnetic separation and beyond [Internet]. Green Chemistry. 2014 ; 16( 6): 2906-2933.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c4gc00164h
  • Fonte: Green Chemistry. Unidade: ESALQ

    Assuntos: CELULOSE, FERMENTAÇÃO, HIDRÓLISE, INIBIDORES QUÍMICOS, LIGNINA, MEMBRANAS DE SEPARAÇÃO, POLÍMEROS (QUÍMICA ORGÂNICA), QUÍMICA VERDE, SACCHAROMYCES

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      GREER, Douglas R et al. Fermentation of hydrolysate detoxified by pervaporation through block copolymer membranes. Green Chemistry, v. 16, p. 4206-4213, 2014Tradução . . Disponível em: https://doi.org/10.1039/c4gc00756e. Acesso em: 03 dez. 2025.
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      Greer, D. R., Basso, T. P., Ibanez, A. B., Bauer, S., Skerker, J. M., Ozcam, A. E., et al. (2014). Fermentation of hydrolysate detoxified by pervaporation through block copolymer membranes. Green Chemistry, 16, 4206-4213. doi:10.1039/c4gc00756e
    • NLM

      Greer DR, Basso TP, Ibanez AB, Bauer S, Skerker JM, Ozcam AE, Leon D, Shin C, Arkin AP, Balsara NP. Fermentation of hydrolysate detoxified by pervaporation through block copolymer membranes [Internet]. Green Chemistry. 2014 ; 16 4206-4213.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c4gc00756e
    • Vancouver

      Greer DR, Basso TP, Ibanez AB, Bauer S, Skerker JM, Ozcam AE, Leon D, Shin C, Arkin AP, Balsara NP. Fermentation of hydrolysate detoxified by pervaporation through block copolymer membranes [Internet]. Green Chemistry. 2014 ; 16 4206-4213.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c4gc00756e
  • Fonte: Green Chemistry. Unidade: IQ

    Assuntos: HIDROGENAÇÃO, QUÍMICA INORGÂNICA

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      UBERMAN, Paula M et al. A recoverable Pd nanocatalyst for selective semi-hydrogenation of alkynes: hydrogenation of benzyl-propargylamines as a challenging model. Green Chemistry, v. 16, p. 4566-4574, 2014Tradução . . Disponível em: https://doi.org/10.1039/c4gc00669k. Acesso em: 03 dez. 2025.
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      Uberman, P. M., Costa, N. J. S., Philippot, K., Carmona, R. C., Santos, A. A. dos, & Rossi, L. M. (2014). A recoverable Pd nanocatalyst for selective semi-hydrogenation of alkynes: hydrogenation of benzyl-propargylamines as a challenging model. Green Chemistry, 16, 4566-4574. doi:10.1039/c4gc00669k
    • NLM

      Uberman PM, Costa NJS, Philippot K, Carmona RC, Santos AA dos, Rossi LM. A recoverable Pd nanocatalyst for selective semi-hydrogenation of alkynes: hydrogenation of benzyl-propargylamines as a challenging model [Internet]. Green Chemistry. 2014 ; 16 4566-4574.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c4gc00669k
    • Vancouver

      Uberman PM, Costa NJS, Philippot K, Carmona RC, Santos AA dos, Rossi LM. A recoverable Pd nanocatalyst for selective semi-hydrogenation of alkynes: hydrogenation of benzyl-propargylamines as a challenging model [Internet]. Green Chemistry. 2014 ; 16 4566-4574.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c4gc00669k
  • Fonte: Green Chemistry. Unidade: EESC

    Assuntos: POLÍMEROS (MATERIAIS), POLIMERIZAÇÃO

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      GANDINI, Alessandro e LACERDA, Talita Martins e CARVALHO, Antonio Jose Felix. A straightforward double coupling of furan moieties onto epoxidized triglycerides: synthesis of monomers based on two renewable resources. Green Chemistry, v. 15, p. 1514-1519, 2013Tradução . . Disponível em: https://doi.org/10.1039/c3gc40358k. Acesso em: 03 dez. 2025.
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      Gandini, A., Lacerda, T. M., & Carvalho, A. J. F. (2013). A straightforward double coupling of furan moieties onto epoxidized triglycerides: synthesis of monomers based on two renewable resources. Green Chemistry, 15, 1514-1519. doi:10.1039/c3gc40358k
    • NLM

      Gandini A, Lacerda TM, Carvalho AJF. A straightforward double coupling of furan moieties onto epoxidized triglycerides: synthesis of monomers based on two renewable resources [Internet]. Green Chemistry. 2013 ; 15 1514-1519.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c3gc40358k
    • Vancouver

      Gandini A, Lacerda TM, Carvalho AJF. A straightforward double coupling of furan moieties onto epoxidized triglycerides: synthesis of monomers based on two renewable resources [Internet]. Green Chemistry. 2013 ; 15 1514-1519.[citado 2025 dez. 03 ] Available from: https://doi.org/10.1039/c3gc40358k

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