A low-cost green approach for synthesis of lead oxide from waste lead ash for use in new lead-acid batteries

doi:10.1016/j.cjche.2018.10.006

摘要/Abstract

摘要： This paper proposes a novel method relating to the recycling of waste lead ash originated from procedure of lead alloy production. The spent lead ash was first disposed by acetic acid leaching system, where lead ash structure wrapping impurities would be destroyed. The synthesis of lead oxide products was conducted at a lower temperature of 90℃. The effect of molar ratio of CH₃COOH to lead content of the ash on leaching efficiency was studied through the acetic acid leaching system. The results demonstrate that 84.6% of lead could be obtained in the leaching solution, while merely 0.7% of Fe blend in solution within a leaching time of 120 min. In the stage of lead oxide synthesis from leaching solution, the yield of lead oxide products could reach up to 94.4% when the molar ratio of NaOH to lead in filtrate was 2.5. This novel green method could shed light on the reuse of lead from exhausted ash with a much more convenient and environmentally friendly procedure.

关键词: Waste lead ash, Leaching, Acetic acid, Solution synthesis, Lead Oxide products

Abstract: This paper proposes a novel method relating to the recycling of waste lead ash originated from procedure of lead alloy production. The spent lead ash was first disposed by acetic acid leaching system, where lead ash structure wrapping impurities would be destroyed. The synthesis of lead oxide products was conducted at a lower temperature of 90℃. The effect of molar ratio of CH₃COOH to lead content of the ash on leaching efficiency was studied through the acetic acid leaching system. The results demonstrate that 84.6% of lead could be obtained in the leaching solution, while merely 0.7% of Fe blend in solution within a leaching time of 120 min. In the stage of lead oxide synthesis from leaching solution, the yield of lead oxide products could reach up to 94.4% when the molar ratio of NaOH to lead in filtrate was 2.5. This novel green method could shed light on the reuse of lead from exhausted ash with a much more convenient and environmentally friendly procedure.

Key words: Waste lead ash, Leaching, Acetic acid, Solution synthesis, Lead Oxide products

Wei Zhang, Gang Tang, Xiaoqin Xiang, Renyu Wang, Shuangquan Gao, Xinfeng Zhu, Qiting Zuo. A low-cost green approach for synthesis of lead oxide from waste lead ash for use in new lead-acid batteries[J]. 中国化学工程学报, 2019, 27(7): 1674-1679.

参考文献

[1] M. López-Abelairas, M. García-Torreiro, T. Lú-Chau, J.M. Lema, A. Steinbüchel, Comparison of several methods for the separation of poly(3-hydroxybutyrate) from Cupriavidus necator H16 cultures, Biochem. Eng. J. 93(2015) 250-259.
[2] J. Chen, L. Zhang, J. Chen, G. Chen, Biosynthesis and characterization of polyhydroxyalkanoate copolyesters in Ralstonia eutropha PHB-4 harboring a low-substrate-specificity PHA synthase PhaC2 Ps from Pseudomonas stutzeri 13171, Chin. J. Chem. Eng. 15(3) (2007) 391-396.
[3] Y. Wang, J. Yin, G.Q. Chen, Polyhydroxyalkanoates, challenges and opportunities, Curr. Opin. Biotechnol. 30(30) (2014) 59-65.
[4] M.S. Le, Z. Manfred, E. Thomas, T.M. Linda, Q. Ren, Production of mediumchain-length polyhydroxyalkanoates by sequential feeding of xylose and octanoic acid in engineered Pseudomonas putida KT2440, BMC Biotechnol. 12(1) (2012) 53-64.
[5] B.C. Saha, Hemicellulose bioconversion, J. Ind. Microbiol. Biotechnol. 30(5) (2003) 279-291.
[6] N. Poomipuk, A. Reungsang, P. Plangklang, Poly-b-hydroxyalkanoates production from cassava starch hydrolysate by Cupriavidus sp. KKU38, Int. J. Biol. Macromol. 65(2014) 51-64.
[7] H.S. Kim, Y.H. Oh, Y.A. Jang, K.H. Kang, Y. David, J.H. Yu, B.K. Song, J.I. Choi, Y.K. Chang, J.C. Joo, Recombinant Ralstonia eutropha engineered to utilize xylose and its use for the production of poly(3-hydroxybutyrate) from sunflower stalk hydrolysate solution, Microb. Cell Factories 15(1) (2016) 95-107.
[8] D. Queirós, S. Rossetti, L.S. Serafim, PHA production by mixed cultures:A way to valorize wastes from pulp industry, Bioresour. Technol. 157(4) (2014) 197-205.
[9] L. Huang, L. Chang, Y. Liu, X. Jia, The composition analysis and preliminary cultivation optimization of a PHA-producing microbial consortium with xylose as a sole carbon source, Waste Manag. 52(2016) 77-85.
[10] V.S.R.K. Ganduri, S. Ghosh, P.R. Patnaik, Mixing control as a device to increase PHB production in batch fermentations with co-cultures of Lactobacillus delbrueckii and Ralstonia eutropha, Process Biochem. 40(1) (2005) 257-264.
[11] F. Cerrone, S.K. Choudhari, R. Davis, D. Cysneiros, V. O'Flaherty, G. Duane, E. Casey, M.W. Guzik, S.T. Kenny, R.P. Babu, Medium chain length polyhydroxyalkanoate (mcl-PHA) production from volatile fatty acids derived from the anaerobic digestion of grass, Appl. Microbiol. Biotechnol. 98(2) (2014) 611-620.
[12] A. Elain, F.M. Le, Y.M. Corre, G.A. Le, T.V. Le, J.L. Audic, S. Bruzaud, Rapid and qualitative fluorescence-based method for the assessment of PHA production in marine bacteria during batch culture, World J. Microbiol. Biotechnol. 31(10) (2015) 1555-1563.
[13] D.K. Kang, C.R. Lee, S.H. Lee, J.H. Bae, Y.K. Park, Y.H. Rhee, B.H. Sung, J.H. Sohn, Production of polyhydroxyalkanoates from sludge palm oil using Pseudomonas putida S12, J. Microbiol. Biotechnol. 27(5) (2017) 990-994.
[14] R. Davis, R. Kataria, F. Cerrone, T. Woods, S. Kenny, A. O'Donovan, M. Guzik, H. Shaikh, G. Duane, V.K. Gupta, Conversion of grass biomass into fermentable sugars and its utilization for medium chain length polyhydroxyalkanoate (mcl-PHA) production by Pseudomonas strains, Bioresour. Technol. 150(4) (2013) 202-209.
[15] J. Mozejko, A. Wilke, G. Przybyłek, S. Ciesielski, Mcl-PHAs produced by Pseudomonas sp. Gl01 using fed-batch cultivation with waste rapeseed oil as carbon source, J. Microbiol. Biotechnol. 22(3) (2012) 371-377.
[16] Y. Luo, J. Xiao, Y. Wang, J. Xu, S. Xie, J. Xu, Streptomyces indicus sp. nov., an actinomycete isolated from deep-sea sediment, Int. J. Syst. Evol. Microbiol. 61(11) (2011) 2712-2716.
[17] C. Gao, Q. Qi, C. Madzak, C.S. Lin, Exploring medium-chain-length polyhydroxyalkanoates production in the engineered yeast Yarrowia lipolytica, J. Ind. Microbiol. Biotechnol. 42(9) (2015) 1255-1262.
[18] L. Finkler, Y.P. Ginoris, C.L. Luna, T.L. Alves, J.C. Pinto, M.A.Z. Coelho, Morphological characterization of Cupriavidus necator DSM 545 flocs through image analysis, World J. Microbiol. Biotechnol. 23(6) (2007) 801-808.
[19] H.W. Ryu, K.U. Cho, E.G. Lee, Y.K. Chang, Recovery of poly(3-ydroxybutyrate) from coagulated Ralstonia eutropha using a chemical digestion method, Biotechnol. Prog. 16(4) (2010) 676-679.
[20] H.W. Ryu, K.S. Cho, Y.K. Chang, H.N. Chang, Cell separation from high cell density broths of Alcaligenes eutrophus by using a coagulant, Biotechnol. Tech. 10(12) (1996) 899-904.
[21] I. Lupescu, M.C. Eremia, G.V. Savoiu, M. Spiridon, D. Panaitescu, C. Nicolae, M.G. Vladu, A. Stefaniu, Comparative studies on isolation of medium-chain-length Polyhydroxyalkanoates produced by Pseudomonas spp. strains, Rev. Chim. 67(10) (2016) 1957-1962.
[22] X.M. Liu, G.P. Sheng, J. Wang, H.Q. Yu, Quantifying the surface characteristics and flocculability of Ralstonia eutropha, Appl. Microbiol. Biotechnol. 79(2) (2008) 187-194.
[23] G. Abu-Elreesh, S. Zaki, S. Farag, M.F. Elkady, D. Abd-El-Haleem, Exobiopolymer from polyhydroxyalkanoate-producing transgenic yeast, Afr. J. Biotechnol. 10(34) (2013) 6558-6563.
[24] K. Goossens, R. Willaert, Flocculation protein structure and cell-cell adhesion mechanism in Saccharomyces cerevisiae, Biotechnol. Lett. 32(11) (2010) 1571-1585.
[25] F. Bidard, M. Bony, B. Blondin, S. Dequin, P. Barre, The Saccharomyces cerevisiae FLO1 flocculation gene encodes for a cell surface protein, Yeast 11(9) (1995) 809-822.
[26] M.C. Bester, D. Jacobson, F.F. Bauer, Many Saccharomyces cerevisiae cell wall protein encoding genes are coregulated by Mss11, but cellular adhesion phenotypes appear only Flo protein dependent, G32(1) (2012) 131-141.
[27] O. Kobayashi, H. Yoshimoto, H. Sone, Analysis of the genes activated by the FLO8 gene in Saccharomyces cerevisiae, Curr. Genet. 36(5) (1999) 256-261.
[28] J.D. Romano, R. Kolter, Pseudomonas-Saccharomyces interactions:Influence of fungal metabolism on bacterial physiology and survival, J. Bacteriol. 187(3) (2005) 940-948.
[29] T. Yuan, Y. Guo, J. Dong, T. Li, T. Zhou, K. Sun, M. Zhang, Q. Wu, Z. Xie, Y. Cai, Construction, characterization and application of a genome-wide promoter library in Saccharomyces cerevisiae, Front. Chem. Sci. Eng. 11(1) (2017) 107-116.
[30] P. Kahar, E.I. Riyanti, H. Otsuka, H. Matsumoto, C. Kihira, C. Ogino, A. Kondo, Challenges of non-flocculating Saccharomyces cerevisiae haploid strain against inhibitory chemical complex for ethanol production, Bioresour. Technol. 245((2017) 1436-1446.
[31] K. Ulaganathan, S. Goud, M. Reddy, U. Kayalvili, Genome engineering for breaking barriers in lignocellulosic bioethanol production, Renew. Sust. Energ. Rev. 74(2017) 1080-1107.
[32] D. Gonzálezramos, A.R.G.D. Vries, S.S. Grijseels, M.C. Berkum, S. Swinnen, M. Broek, E. Nevoigt, J.M.G. Daran, J.T. Pronk, A.J.A. Maris, A new laboratory evolution approach to select for constitutive acetic acid tolerance in Saccharomyces cerevisiae and identification of causal mutations, Biotechnol. Biofuels 9(1) (2016) 173-190.
[33] H.S. Kim, N.R. Kim, W. Kim, W. Choi, Insertion of transposon in the vicinity of SSK2 confers enhanced tolerance to furfural in Saccharomyces cerevisiae, Appl. Microbiol. Biotechnol. 95(2) (2012) 531-540.
[34] G. Du, J. Yu, Metabolic analysis on fatty acid utilization by Pseudomonas oleovorans:mcl-Poly(3-hydroxyalkanoates) synthesis versus b-oxidation, Process Biochem. 38(3) (2002) 325-332.
[35] J.J. Bozzola, L.D. Russell, Electron Microscopy:Principles and Techniques for Biologists, Jones and Bartlett, 1999.
[36] P. Thonart, M. Custinne, M. Paquot, Zeta potential of yeast cells:Application in cell immobilization, Enzyme Microb. Technol. 4(3) (1982) 191-194.
[37] W.Y. Lu, T. Zhang, D.Y. Zhang, C.H. Li, J.P. Wen, L.X. Du, A novel bioflocculant produced by Enterobacter aerogenes and its use in defecating the trona suspension, Biochem. Eng. J. 27(1) (2006) 1-7.
[38] H. Ito, Y. Fukuda, K. Murata, A. Kimura, Transformation of intact yeast cells treated with alkali cations, J. Agric. Chem. Soc. Jpn. 48(2) (1983) 341-347.
[39] S. Taguchi, M. Yamada, K.I. Matsumoto, K. Tajima, Y. Satoh, M. Munekata, K. Ohno, K. Kohda, T. Shimamura, H. Kambe, A microbial factory for lactate-based polyesters using a lactate-polymerizing enzyme, Proc. Natl. Acad. Sci. U.S.A. 105(45) (2008) 17323-17327.
[40] A. Hokamura, I. Wakida, Y. Miyahara, T. Tsuge, H. Shiratsuchi, K. Tanaka, H. Matsusaki, Biosynthesis of poly(3-hydroxybutyrate-co-3-hydroxyalkanoates) by recombinant Escherichia coli from glucose, J. Biosci. Bioeng. 120(3) (2015) 305-310.
[41] X.X. Wei, F. Liu, J. Jian, R.Y. Wang, G.Q. Chen, Production of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) by recombinant Pseudomonas stutzeri 1317 from unrelated carbon sources, Chin. J. Chem. Eng. 21(9) (2013) 1057-1061.
[42] Z. Zheng, Q. Gong, G.Q. Chen, A novel method for production of 3-hydroxydecanoic acid by recombinant Escherichia coli and Pseudomonas putida, Chin. J. Chem. Eng. 12(4) (2004) 550-555.
[43] Y. Wang, H. Wu, X. Jiang, G.Q. Chen, Engineering Escherichia coli for enhanced production of poly(3-hydroxybutyrate-co-4-hydroxybutyrate) in larger cellular space, Metab. Eng. 25(2014) 183-193.
[44] S. Ohji, A. Yamazoe, A. Hosoyama, K. Tsuchikane, T. Ezaki, N. Fujita, The complete genome sequence of Pseudomonas putida NBRC 14164 confirms high intraspecies variation, Genome Announc. 2(1) (2014) e00029-14.
[45] G.Q. Chen, X.R. Jiang, Y. Guo, Synthetic biology of microbes synthesizing polyhydroxyalkanoates (PHA), Synth. Syst. Biotechnol. 1(4) (2016) 236-242.
[46] J. Zhou, Q. Ma, H. Yi, L. Wang, H. Song, Y.J. Yuan, Metabolome profiling reveals metabolic cooperation between Bacillus megaterium and Ketogulonicigenium vulgare during induced swarm motility, Appl. Environ. Microbiol. 77(19) (2011) 7023-7030.
[47] J. Du, W. Bai, H. Song, Y.J. Yuan, Combinational expression of sorbose/sorbosone dehydrogenases and cofactor pyrroloquinoline quinone increases 2-keto-l-gulonic acid production in Ketogulonigenium vulgareBacillus cereus consortium, Metab. Eng. 19(2013) 50-56.
[48] A. Prindle, P. Samayoa, I. Razinkov, T. Danino, L.S. Tsimring, J. Hasty, Sensing array of radically coupled genetic biopixels, Nature 481(7379) (2012) 39-44.
[49] A.A. Eddy, A.D. Rudin, Part of the yeast surface apparently involved in flocculation, J. Inst. Brew. 64(1) (1958) 19-21.
[50] B.L. Miki, N.H. Poon, A.P. James, V.L. Seligy, Possible mechanism for flocculation interactions governed by gene FLO1 in Saccharomyces cerevisiae, J. Bacteriol. 150(2) (1982) 878-889.