Abstract

References

• [1] B. A. de Marco, B. S. Rechelo, E. G. Tótoli, A. C. Kogawa, and H. R. N. Salgado. (2019). “Evolution of green chemistry and its multidimensional impacts: A review”. Saudi Pharmaceutical Journal. 27 (1): 1–8. 10.1016/j.jsps.2018.07.011.

  DOI: https://doi.org/10.1016/j.jsps.2018.07.011

• [2] S. K. Singh, D. N. Rao, M. Agrawal, J. Pandey, and D. Naryan. (1991). “Air pollution tolerance index of plants”. Journal of Environmental Management. 32 (1): 45–55, 1991, doi: 10.1016/S0301-4797(05)80080-5.

  DOI: https://doi.org/10.1016/S0301-4797(05)80080-5

• [3] C. J. Li and B. M. Trost. (2008). “Green chemistry for chemical synthesis”. Proceedings of the National Academy of Sciences of the United States of America. 105 (36): 13197–13202. 10.1073/pnas.0804348105.

  DOI: https://doi.org/10.1073/pnas.0804348105

• [4] J. B. Manley, P. T. Anastas, and B. W. Cue. (2008). “Frontiers in Green Chemistry: meeting the grand challenges for sustainability in R&D and manufacturing”. Journal of Cleaner Production. 16 (6): 743–750. 10.1016/j.jclepro.2007.02.025.

  DOI: https://doi.org/10.1016/j.jclepro.2007.02.025

• [5] M. Poliakoff, J. M. Fitzpatrick, T. R. Farren, and P. T. Anastas. (2002). “Green chemistry: Science and politics of change”. Science. 297 (5582): 807–810. 10.1126/science.297.5582.807.

  DOI: https://doi.org/10.1126/science.297.5582.807

• [6] M. J. Mulvihill, E. S. Beach, J. B. Zimmerman, and P. T. Anastas. (2011). “Green chemistry and green engineering: A framework for sustainable technology development”. Annual Review of Environment and Resources. 36: 271–293. 10.1146/annurev-environ-032009-095500.

  DOI: https://doi.org/10.1146/annurev-environ-032009-095500

• [7] J. A. Linthorst. (2010). “An overview: Origins and development of green chemistry”. Foundations of Chemistry. 12 (1): 55–68. 10.1007/s10698-009-9079-4.

  DOI: https://doi.org/10.1007/s10698-009-9079-4

• [8] P. Anastas and N. Eghbali. (2020). “Green Chemistry: Principles and Practise”. Chemical Society Reviews. 29: 301–12. 10.1039/b918763b.

  DOI: https://doi.org/10.1039/B918763B

• [9] L. Giusti. (2009). “A review of waste management practices and their impact on human health”. Waste Management. 29 (8): 2227–2239. 10.1016/j.wasman.2009.03.028.

  DOI: https://doi.org/10.1016/j.wasman.2009.03.028

• [10] C. Brown, M. Milke, and E. Seville. (2011). “Disaster waste management: A review article”. Waste Management. 31 (6): 1085–1098. 10.1016/j.wasman.2011.01.027.

  DOI: https://doi.org/10.1016/j.wasman.2011.01.027

• [11] M. Tobiszewski, M. Marć, A. Gałuszka, and J. Namies̈nik. (2015). “Green chemistry metrics with special reference to green analytical chemistry”. Molecules. 20 (6): 10928–10946. 10.3390/molecules200610928.

  DOI: https://doi.org/10.3390/molecules200610928

• [12] T. Hudlicky, D. A. Frey, L. Koroniak, C. D. Claeboe, and L. E. Brammer Jr. (1999). “Toward a ‘reagent-free’ synthesis”. Green Chemistry. 1 (2): 57–59. 10.1039/a901397k.

  DOI: https://doi.org/10.1039/a901397k

• [13] B. M. Trost. (1995). “Atom Economy—A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way”. Angewandte Chemie International Edition in English. 34 (3): 259–281. 10.1002/anie.199502591.

  DOI: https://doi.org/10.1002/anie.199502591

• [14] K. van Aken, L. Strekowski, and L. Patiny. (2006). “EcoScale, a semi-quantitative tool to select an organic preparation based on economical and ecological parameters”. Beilstein Journal of Organic Chemistry. 2. 10.1186/1860-5397-2-3.

  DOI: https://doi.org/10.1186/1860-5397-2-3

• [15] R. A. Sheldon. (2007). “The E Factor: Fifteen years on”. Green Chemistry. 9 (12): 1273–1283. 10.1039/b713736m.

  DOI: https://doi.org/10.1039/b713736m

• [16] Y. Lie, P. Ortiz, R. Vendamme, K. Vanbroekhoven, and T. J. Farmer. (2019). “BioLogicTool: A Simple Visual Tool for Assisting in the Logical Selection of Pathways from Biomass to Products”. Industrial and Engineering Chemistry Research. 58 (35): 15945–15957. 10.1021/acs.iecr.9b00575.

  DOI: https://doi.org/10.1021/acs.iecr.9b00575

• [17] Y. S. Kurniawan, M. Anwar, and T. D. Wahyuningsih. (2017). “New lubricant from used cooking oil: Cyclic ketal of ethyl 9,10-dihydroxyoctadecanoate”. Materials Science Forum. 901: 135–141. 10.4028/www.scientific.net/MSF.901.135.

  DOI: https://doi.org/10.4028/www.scientific.net/MSF.901.135

• [18] J. Jumina, Y. Priastomo, H. R. Setiawan, Mutmainah, Y. S. Kurniawan and K. Ohto. (2020). “Simultaneous removal of lead(II), chromium(III) and copper(II) heavy metal ions through an adsorption process using C-phenylcalix[4] pyrogallolarene material”. Journal of Environmental Chemical Engineering. 8: 103971. 10.1016/j.jece.2020.103971.

  DOI: https://doi.org/10.1016/j.jece.2020.103971

• [19] L. G. C. Villegas, N. Mashhadi, M. Chen, D. Mukherjee, K. E. Taylor and N. Biswas. (2016). “A Short Review of Techniques for Phenol Removal from Wastewater”. Current Pollution Reports. 2 (3): 157–167. 10.1007/s40726-016-0035-3.

  DOI: https://doi.org/10.1007/s40726-016-0035-3

• [20] Y. S. Kurniawan, K. Anggraeni, R. Indrawati, and L. Yuliati. (2020). “Functionalization of titanium dioxide through dye sensitizing method utilizing red amaranth extract for phenol photodegradation”. IOP Conference Series: Materials Science and Engineering.

• [21] D. Ariyanti, D. Iswantini, P. Sugita, N. Nurhidayat, and Y. S. Kurniawan. (2020). “Highly Sensitive Phenol Biosensor Utilizing Selected Bacillus Biofilm Through an Electrochemical Method”. Makara Journal of Science. 24 (1). 10.7454/mss.v24i1.11726.

  DOI: https://doi.org/10.7454/mss.v24i1.11726

• [22] M. M. Khan, S. F. Adil, and A. Al-Mayouf. (2015). “Metal oxides as photocatalysts”. Journal of Saudi Chemical Society. 19 (5): 462–464. 10.1016/j.jscs.2015.04.003.

  DOI: https://doi.org/10.1016/j.jscs.2015.04.003

• [23] A. Loupy. (2017). “Solvent-Free Microwave Organic Synthesis as an Efficient Procedure for Green Chemistry”. ChemInform. 36 (10). 10.1002/chin.200510294.

  DOI: https://doi.org/10.1002/chin.200510294

• [24] M. Vian, C. Breil, L. Vernes, E. Chaabani, and F. Chemat. (2017). “Green solvents for sample preparation in analytical chemistry”. Current Opinion in Green and Sustainable Chemistry. 5: 44–48. 10.1016/j.cogsc.2017.03.010.

  DOI: https://doi.org/10.1016/j.cogsc.2017.03.010

• [25] P. J. Walsh, H. Li, and C. Anaya de Parrodi. (2007). “A Green Chemistry Approach to Asymmetric Catalysis: Solvent-Free and Highly Concentrated Reactions”. ChemInform. 38 (36). 10.1002/chin.200736264.

  DOI: https://doi.org/10.1002/chin.200736264

• [26] I. Pacheco-Fernández and V. Pino. (2019). “Green solvents in analytical chemistry”. Current Opinion in Green and Sustainable Chemistry. 18: 42–50. 10.1016/j.cogsc.2018.12.010.

  DOI: https://doi.org/10.1016/j.cogsc.2018.12.010

• [27] F. P. Byrne, S. Jin, G. Paggiola, T. H. M. Petchey, J. H. Clark, T. J. Farmer, A. J. Hunt, C. Robert McElroy, J. Sherwood. (2016). “Tools and techniques for solvent selection: green solvent selection guides”. Sustainable Chemical Processes. 4 (1). 10.1186/s40508-016-0051-z.

  DOI: https://doi.org/10.1186/s40508-016-0051-z

• [28] C. Jiménez-Gonzalez, A. D. Curzons, D. J. C. Constable, and V. L. Cunningham. (2004). “Expanding GSK’s Solvent Selection Guide - Application of life cycle assessment to enhance solvent selections”. Clean Technologies and Environmental Policy. 7 (1): 42–50. 10.1007/s10098-004-0245-z.

  DOI: https://doi.org/10.1007/s10098-004-0245-z

• [29] A. Duereh, Y. Sato, R. L. Smith, and H. Inomata. (2017). “Methodology for replacing dipolar aprotic solvents used in API processing with safe hydrogen-bond donor and acceptor solvent-pair mixtures”. Organic Process Research and Development. 21 (1): 114–124. 10.1021/acs.oprd.6b00401.

  DOI: https://doi.org/10.1021/acs.oprd.6b00401

• [30] R. Schlögl. (2016). “Sustainable Energy Systems: The Strategic Role of Chemical Energy Conversion”. Topics in Catalysis. 59 (8): 772–786. 10.1007/s11244-016-0551-9.

  DOI: https://doi.org/10.1007/s11244-016-0551-9

• [31] J. Jumina, H. R. Setiawan, S. Triono, Y. S. Kurniawan, Y. Priastomo. (2020). “C -Arylcalix[4]pyrogallolarene Sulfonic Acid: A Novel and Efficient Organocatalyst Material for Biodiesel Production”. Bulletin of the Chemical Society of Japan. 93 (2): 252–259. 10.1246/bcsj.20190275.

  DOI: https://doi.org/10.1246/bcsj.20190275

• [32] G. J. Hutchings. (2007). “A golden future for green chemistry”. Catalysis Today. 122 (3): 196–200. 10.1016/j.cattod.2007.01.018.

  DOI: https://doi.org/10.1016/j.cattod.2007.01.018

• [33] P. A. Deyris and C. Grison. (2018). “Nature, ecology and chemistry: An unusual combination for a new green catalysis, ecocatalysis”. Current Opinion in Green and Sustainable Chemistry. 10: 6–10. 10.1016/j.cogsc.2018.02.002.

  DOI: https://doi.org/10.1016/j.cogsc.2018.02.002

• [34] G. Chatel. (2018). “How sonochemistry contributes to green chemistry?”. Ultrasonics Sonochemistry. 40: 117–122. 10.1016/j.ultsonch.2017.03.029.

  DOI: https://doi.org/10.1016/j.ultsonch.2017.03.029

• [35] Díaz-Ortiz, P. Prieto, and A. de la Hoz. (2019). “A Critical Overview on the Effect of Microwave Irradiation in Organic Synthesis”. Chemical Record. 19 (1): 85–97. 10.1002/tcr.201800059.

  DOI: https://doi.org/10.1002/tcr.201800059

• [36] F. Mavandadi and Å. Pilotti. (2006). “The impact of microwave-assisted organic synthesis in drug discovery”. Drug Discovery Today. 11 (3): 165–174. 10.1016/S1359-6446(05)03695-0.

  DOI: https://doi.org/10.1016/S1359-6446(05)03695-0

• [37] M. Oelgemöller and N. Hoffmann. (2016). “Studies in organic and physical photochemistry-an interdisciplinary approach”. Organic and Biomolecular Chemistry. 14 (31): 7392–7442. 10.1039/c6ob00842a.

  DOI: https://doi.org/10.1039/C6OB00842A

• [38] H. Trommsdorff. (1834). “Ueber Santonin”. Annalen der Pharmacie. 11 (2): 190–207. 10.1002/jlac.18340110207.

  DOI: https://doi.org/10.1002/jlac.18340110207

• [39] J. M. Herrmann, C. Duchamp, M. Karkmaz, B. T. Hoai, H. Lachheb, E. Puzenat, C. Guillard. (2007). “Environmental green chemistry as defined by photocatalysis,” Journal of Hazardous Materials. 146 (3): 624–629. 10.1016/j.jhazmat.2007.04.095.

  DOI: https://doi.org/10.1016/j.jhazmat.2007.04.095

• [40] Y. S. Kurniawan, A. C. Imawan, S. R. Rao, K. Ohto, W. Iwasaki, M. Miyazaki and J. Jumina. (2019). “Microfluidics era in chemistry field: A review”. Journal of the Indonesian Chemical Society. 2 (1): 7-23. 10.34311/jics.2019.02.1.7.

  DOI: https://doi.org/10.34311/jics.2019.02.1.7

• [41] Y.S. Kurniawan, R. R. Sathuluri, and K. Ohto. (2020). “Droplet microfluidic device for rapid and efficient metal separation using host-guest chemistry”. In Advances in Microfluidic Technologies for Energy and Environmental Applications. IntechOpen. 10.5772/intechopen.89846.

  DOI: https://doi.org/10.5772/intechopen.89846

• [42] J. I. Yoshida, H. Kim, and A. Nagaki. (2011). “Green and sustainable chemical synthesis using flow microreactors”. ChemSusChem. 4 (3): 331–340. 10.1002/cssc.201000271.

  DOI: https://doi.org/10.1002/cssc.201000271

• [43] J. I. Yoshida, H. Kim, and A. Nagaki. (2017). “‘Impossible’ Chemistries Based on Flow and Micro”. Journal of Flow Chemistry. 7 (3): 60–64. 10.1556/1846.2017.00017.

  DOI: https://doi.org/10.1556/1846.2017.00017

• [44] H. Kim, A. Nagaki, and J. I. Yoshida. (2011). “A flow-microreactor approach to protecting-group-free synthesis using organolithium compounds”. Nature Communications. 2 (1). 10.1038/ncomms1264.

  DOI: https://doi.org/10.1038/ncomms1264

• [45] A. C. Imawan, Y. S. Kurniawan, M. F. Lukman, Jumina, Triyono, and D. Siswanta. (2018). “Synthesis and kinetic study of the urea controlled release composite material: Sodium lignosulfonate from isolation of wood sawdust-sodium Alginate-Tapioca”. Indonesian Journal of Chemistry. 18 (1): 108–115. 10.22146/ijc.26597.

  DOI: https://doi.org/10.22146/ijc.26597

• [46] J. Jumina, Y. Yasodhara, S. Triono, Y. S. Kurniawan, Y. Priastomo, H. M. Chawla, and N. Kumar. (2021). “Preparation and evaluation of α-cellulose based new heterogenous catalyst for production of biodiesel”. Journal of Applied Polymer Science. 138 (2): 49658. 10.1002/app.49658.

  DOI: https://doi.org/10.1002/app.49658

• [47] J. Yan, X. Pan, Z. Wang, Z. Lu, Y. Wang, L. Liu, J. Zhang, C. Ho, M. R. Bockstaller, K. Matyjaszewski. (2017). “A Fatty Acid-Inspired Tetherable Initiator for Surface-Initiated Atom Transfer Radical Polymerization”. Chemistry of Materials. 29 (11): 4963–4969. 10.1021/acs.chemmater.7b01338.

  DOI: https://doi.org/10.1021/acs.chemmater.7b01338

• [48] R. A. Sheldon. (2016). “Green chemistry, catalysis and valorization of waste biomass”. Journal of Molecular Catalysis A: Chemical. 422: 3–12. 10.1016/j.molcata.2016.01.013.

  DOI: https://doi.org/10.1016/j.molcata.2016.01.013

• [49] F. J. Lozano, R. Lozano, P. Freire, C. Jiménez-Gonzalez, T. Sakao, M. G. Ortiz, A. Trianni, A. Carpenter, T. Viveros. (2018). “New perspectives for green and sustainable chemistry and engineering: Approaches from sustainable resource and energy use, management, and transformation”. Journal of Cleaner Production. 172: 227–232. 10.1016/j.jclepro.2017.10.145.

  DOI: https://doi.org/10.1016/j.jclepro.2017.10.145

• [50] T. D. Wahyuningsih and Y. S. Kurniawan. (2017). “Green synthesis of some novel dioxolane compounds from Indonesian essential oils as potential biogreases”. AIP Conference Proceedings. 1823. 10.1063/1.4978154.

  DOI: https://doi.org/10.1063/1.4978154

• [51] Y. S. Kurniawan, Y. Ramanda, K. Thomas, Hendra, and T. D. Wahyuningsih. (2017). “Synthesis of 1,4-dioxaspiro[4.4] and 1,4-dioxaspiro[4.5] novel compounds from oleic acid as potential biolubricant”. Indonesian Journal of Chemistry. 17 (2): 301–308. 10.22146/ijc.24891.

  DOI: https://doi.org/10.22146/ijc.24891

• [52] T. D. Wahyuningsih and Y.S. Kurniawan. (2020). “Synthesis of dioxo-dioxane and dioxo-dioxepane ethyl oleate derivatives as bio-lubricant base stocks”. Indonesian Journal of Chemistry. 20 (3): 504-509. 10.22146/ijc.42317.

  DOI: https://doi.org/10.22146/ijc.42317
• [53] T. D. Wahyuningsih, Y. S. Kurniawan, S. Amalia, T. A. K. Wardhani, and C. E. S. Muriningsih. (2019). “Diethanolamide derivatives as a potential enhanced oil recovery agent from indonesian castor oil and used frying oil: Isolation, synthesis, and evaluation as nonionic biosurfactants”. Rasayan Journal of Chemistry. 12 (2): 741–748. 10.31788/RJC.2019.1225140. DOI: https://doi.org/10.31788/RJC.2019.1225140

Paper information