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請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/85339
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor羅世強(Shyh-Chyang Luo)
dc.contributor.authorYu-Zhen Yangen
dc.contributor.author陽玉振zh_TW
dc.date.accessioned2023-03-19T22:58:44Z-
dc.date.copyright2022-08-05
dc.date.issued2022
dc.date.submitted2022-07-26
dc.identifier.citation[1] L. Jiang and J. Zhang, “7 - biodegradable and biobased polymers,” in Applied Plastics Engineering Handbook (Second Edition) (M. Kutz, ed.), Plastics Design Library, pp. 127–143, William Andrew Publishing, second ed., 2017. [2] M. V. Guettler, M. K. Jain, and D. Rumler, “Method for making succinic acid, bacterial variants for use in the process, and methods for obtaining variants,” Nov. 12 1996. US Patent 5,573,931. [3] M. V. Guettler, M. K. Jain, and B. K. Soni, “Process for making succinic acid, microorganisms for use in the process and methods of obtaining the microorganisms,” Apr. 2 1996. US Patent 5,504,004. [4] P. Lee, S. Lee, S. Hong, and H. Chang, “Isolation and characterization of a new succinic acid-producing bacterium, Mannheimia succiniciproducens MBEL55E, from bovine rumen,” Applied Microbiology and Biotechnology, vol. 58, no. 5, pp. 663–668, 2002. [5] H. Ryu, K. Kang, and J. Yun, “Bioconversion of fumarate to succinate using glycerol as a carbon source,” in Twentieth Symposium on Biotechnology for Fuels and Chemicals, pp. 511–520, Springer, 1999. [6] H. Ryu and Y. Wee, “Characterization of bioconversion of fumarate to succinate by alginate immobilized Enterococcus faecalis RKY1,” in Twenty-Second Symposium on Biotechnology for Fuels and Chemicals, pp. 525–535, Springer, 2001. [7] Y. Wee, J. Yun, K. Kang, and H. Ryu, “Continuous production of succinic acid by a fumarate-reducing bacterium immobilized in a hollow-fiber bioreactor,” in Biotechnology for Fuels and Chemicals, pp. 1093–1104, Springer, 2002. [8] G. Vemuri, M. Eiteman, and E. Altman, “Succinate production in dual-phase Escherichia coli fermentations depends on the time of transition from aerobic to anaerobic conditions,” Journal of Industrial Microbiology and Biotechnology, vol. 28, no. 6, pp. 325–332, 2002. [9] L. Agarwal, J. Isar, G. Meghwanshi, and R. Saxena, “A cost effective fermentative production of succinic acid from cane molasses and corn steep liquor by Escherichia coli,” Journal of Applied Microbiology, vol. 100, no. 6, pp. 1348–1354, 2006. [10] P. Lee, S. Lee, S. Hong, and H. Chang, “Batch and continuous cultures of Mannheimia succiniciproducens MBEL55E for the production of succinic acid from whey and corn steep liquor,” Bioprocess and Biosystems Engineering, vol. 26, no. 1, pp. 63–67, 2003. [11] P. Lee, W. Lee, S. Lee, and H. Chang, “Succinic acid production with reduced by-product formation in the fermentation of Anaerobiospirillum succiniciproducens using glycerol as a carbon source,” Biotechnology and Bioengineering, vol. 72, no. 1, pp. 41–48, 2001. [12] S. S. Yazdani and R. Gonzalez, “Anaerobic fermentation of glycerol: a path to economic viability for the biofuels industry,” Current Opinion in Biotechnology, vol. 18, no. 3, pp. 213–219, 2007. [13] N. S. Samuelov, R. Datta, M. K. Jain, and J. G. Zeikus, “Whey fermentation by Anaerobiospirillum succiniciproducens for production of a succinate-based animal feed additive,” Applied and Environmental Microbiology, vol. 65, no. 5, pp. 2260– 2263, 1999. [14] C. Wan, Y. Li, A. Shahbazi, and S. Xiu, “Succinic acid production from cheese whey using Actinobacillus succinogenes 130 Z,” in Biotechnology for Fuels and Chemicals, pp. 111–119, Springer, 2007. [15] Y. Liu, P. Zheng, Z. Sun, Y. Ni, J. Dong, and L. Zhu, “Economical succinic acid production from cane molasses by Actinobacillus succinogenes,” Bioresource Technology, vol. 99, no. 6, pp. 1736–1742, 2008. [16] D. Kim, S. Yim, P. Lee, W. Lee, S. Lee, and H. Chang, “Batch and continuous fermentation of succinic acid from wood hydrolysate by Mannheimia succiniciproducens MBEL55E,” Enzyme and Microbial Technology, vol. 35, no. 6- 7, pp. 648–653, 2004. [17] P. Lee, S. Lee, S. Hong, H. Chang, and S. Park, “Biological conversion of wood hydrolysate to succinic acid by Anaerobiospirillum succiniciproducens,” Biotechnology Letters, vol. 25, no. 2, pp. 111–114, 2003. [18] C. Du, S. C. Lin, A. Koutinas, R. Wang, and C. Webb, “Succinic acid production from wheat using a biorefining strategy,” Applied Microbiology and Biotechnology, vol. 76, no. 6, pp. 1263–1270, 2007. [19] “Bioplastics market data.” Retrieved April 20, 2022, from https://www.european-bioplastics.org/market/. [20] Y. Li, Z. Wang, and T. He, “Morphological control of polymer spherulites via manipulating radial lamellar organization upon evaporative crystallization: a mini review,” Crystals, vol. 7, no. 4, 2017. [21] A. Keller, “The spherulitic structure of crystalline polymers. Part I. Investigations with the polarizing microscope,” Journal of Polymer Science, vol. 17, no. 84, pp. 291–308, 1955. [22] Z. Gan, H. Abe, H. Kurokawa, and Y. Doi, “Solid-state microstructures, thermal properties, and crystallization of biodegradable poly(butylene succinate)(PBS) and its copolyesters,” Biomacromolecules, vol. 2, no. 2, pp. 605–613, 2001. [23] J. Xu and B. Guo, “Microbial succinic acid, its polymer poly(butylene succinate), and applications,” in Plastics from Bacteria, pp. 347–388, Springer, 2010. [24] Y. Ichikawa, H. Kondo, Y. Igarashi, K. Noguchi, K. Okuyama, and J. Washiyama, “Crystal structures of α and β forms of poly(tetramethylene succinate),” Polymer, vol. 41, no. 12, pp. 4719–4727, 2000. [25] K. Cho, J. Lee, and K. Kwon, “Hydrolytic degradation behavior of poly(butylene succinate)s with different crystalline morphologies,” Journal of Applied Polymer Science, vol. 79, no. 6, pp. 1025–1033, 2001. [26] T. Fujimaki, “Processability and properties of aliphatic polyesters,`BIONOLLE' , synthesized by polycondensation reaction,” Polymer Degradation and Stability, vol. 59, no. 1-3, pp. 209–214, 1998. [27] K. Kasuya, K. Takagi, S. Ishiwatari, Y. Yoshida, and Y. Doi, “Biodegradabilities of various aliphatic polyesters in natural waters,” Polymer Degradation and Stability, vol. 59, no. 1-3, pp. 327–332, 1998. [28] N. Ishii, Y. Inoue, T. Tagaya, H. Mitomo, D. Nagai, and K. Kasuya, “Isolation and characterization of poly(butylene succinate)-degrading fungi,” Polymer Degradation and Stability, vol. 93, no. 5, pp. 883–888, 2008. [29] H. Maeda, Y. Yamagata, K. Abe, F. Hasegawa, M. Machida, R. Ishioka, K. Gomi, and T. Nakajima, “Purification and characterization of a biodegradable plastic-degrading enzyme from Aspergillus oryzae,” Applied Microbiology and Biotechnology, vol. 67, no. 6, pp. 778–788, 2005. [30] K. Thirunavukarasu, S. Purushothaman, J. Sridevi, M. Aarthy, M. K. Gowthaman, T. Nakajima-Kambe, and N. R. Kamini, “Degradation of poly(butylene succinate) and poly(butylene succinate-co-butylene adipate) by a lipase from yeast Cryptococcus sp. grown on agro-industrial residues,” International Biodeterioration & Biodegradation, vol. 110, pp. 99–107, 2016. [31] Z. Bai, Y. Liu, T. Su, and Z. Wang, “Effect of hydroxyl monomers on the enzymatic degradation of poly(ethylene succinate), poly(butylene succinate), and poly(hexylene succinate),” Polymers, vol. 10, no. 1, p. 90, 2018. [32] C. Phithakrotchanakoon, R. Daduang, A. Thamchaipenet, T. Wangkam, T. Srikhirin, L. Eurwilaichitr, and V. Champreda, “Heterologous expression of polyhydroxyalkanoate depolymerase from Thermobifida sp. in Pichia pastoris and catalytic analysis by surface plasmon resonance,” Applied Microbiology and Biotechnology, vol. 82, no. 1, pp. 131–140, 2009. [33] D. Meyerhofer, “Characteristics of resist films produced by spinning,” Journal of Applied Physics, vol. 49, no. 7, pp. 3993–3997, 1978. [34] S. Middleman and A. K. Hochberg, Process Engineering: Analysis in Semiconductor Device Fabrication. Mcgraw-Hill College, 1993. [35] D. W. Schubert and T. Dunkel, “Spin coating from a molecular point of view: its concentration regimes, influence of molar mass and distribution,” Materials Research Innovations, vol. 7, no. 5, pp. 314–321, 2003. [36] M. Tyona, “A theoritical study on spin coating technique,” Advances in materials Research, vol. 2, no. 4, p. 195, 2013. [37] A. G. Emslie, F. T. Bonner, and L. G. Peck, “Flow of a viscous liquid on a rotating disk,” Journal of Applied Physics, vol. 29, no. 5, pp. 858–862, 1958. [38] W. Daughton and F. Givens, “An investigation of the thickness variation of spun-on thin films commonly associated with the semiconductor industry,” Journal of The Electrochemical Society, vol. 129, no. 1, p. 173, 1982. [39] Y. Mouhamad, P. Mokarian-Tabari, N. Clarke, R. Jones, and M. Geoghegan, “Dynamics of polymer film formation during spin coating,” Journal of Applied Physics, vol. 116, no. 12, p. 123513, 2014. [40] C. M. Hansen, “The three dimensional solubility parameter,” Danish Technical: Copenhagen, vol. 14, 1967. [41] Y. Liu, J. Zhao, Z. Li, C. Mu, W. Ma, H. Hu, K. Jiang, H. Lin, H. Ade, and H. Yan, “Aggregation and morphology control enables multiple cases of high-efficiency polymer solar cells,” Nature Communications, vol. 5, no. 1, pp. 1–8, 2014. [42] R. G. Larson and T. J. Rehg, “Spin coating,” in Liquid Film Coating, pp. 709–734, Springer, 1997. [43] T. Sekitani, U. Zschieschang, H. Klauk, and T. Someya,“ Flexible organic transistors and circuits with extreme bending stability,” Nature Materials, vol. 9, no. 12, pp. 1015–1022, 2010. [44] Y. Hong, P. Chen, J. Wang, M. Lee, S. Horng, and H. Meng, “Simultaneous enhancement in both large-area coatability and photovoltaic performance of inverted organic solar cells with co-solvent,” Solar Energy Materials and Solar Cells, vol. 120, pp. 197–203, 2014. [45] H. Zhang, K. Darabi, N. Y. Nia, A. Krishna, P. Ahlawat, B. Guo, M. H. S. Almalki, T. Su, D. Ren, V. Bolnykh, et al., “A universal co-solvent dilution strategy enables facile and cost-effective fabrication of perovskite photovoltaics,” Nature Communications, vol. 13, no. 1, pp. 1–12, 2022. [46] P. Hong, S. W. Harun, C. Yi, K. K. Jayapalan, and H. Ahmad, “Dynamic dispersing technique for pr coating process in planar lightwave circuit fabrication,” Microwave and Optical Technology Letters, vol. 49, no. 8, pp. 1993–1995, 2007. [47] Y. Ma, P. Vashishtha, K. Chen, E. L. Peach, D. Ohayon, J. M. Hodgkiss, and J. E. Halpert, “Controlled growth of CH3NH3PbI3 using a dynamically dispensed spin- coating method: Improving efficiency with a reproducible PbI2 Blocking Layer,” ChemSusChem, vol. 10, no. 12, pp. 2677–2684, 2017. [48] Z. Welchel, L. A. DeSilva, and T. Banadara, “Properties of tris(8-hydroxyquinoline) aluminum thin films fabricated by spin coating from static and dynamic dispense methods,” Optical Materials, vol. 108, p. 110447, 2020. [49] P. Sobolewski, N. S. Murthy, J. Kohn, and M. El Fray, “Adsorption of fibrinogen and fibronectin on elastomeric poly(butylene succinate) copolyesters,” Langmuir, vol. 35, no. 26, pp. 8850–8859, 2019. [50] H. Hsieh, N. Wu, T. Chuang, W. Lee, J. Chen, and W. Chen, “Eco-friendly polyfluorene/poly(butylene succinate) blends and their electronic device application on biodegradable substrates,” ACS Applied Polymer Materials, vol. 2, no. 6, pp. 2469–2476, 2020. [51] G. Z. Papageorgiou and D. N. Bikiaris, “Crystallization and melting behavior of three biodegradable poly(alkylene succinates). a comparative study,” Polymer, vol. 46, no. 26, pp. 12081–12092, 2005. [52] U. W. Gedde and M. S. Hedenqvist, Fundamental Polymer Science. Springer, second ed., 2019. [53] F. W. Billmeyer, Textbook of Polymer Science. John Wiley & Sons, 1984. [54] J. D. Hoffman and R. L. Miller, “Kinetic of crystallization from the melt and chain folding in polyethylene fractions revisited: theory and experiment,” Polymer, vol. 38, no. 13, pp. 3151–3212, 1997. [55] U. W. Gedde, Polymer Physics. Chapman & Hall, London, 1995. [56] D. Sadler and G. Gilmer, “A model for chain folding in polymer crystals: rough growth faces are consistent with the observed growth rates,” Polymer, vol. 25, no. 10, pp. 1446–1452, 1984. [57] P. Basu, Biomass Gasification, Pyrolysis and Torrefaction: Practical Design & Theory. Academic Press, 2018. [58] A. Newman and G. Zografi, “Commentary: considerations in the measurement of glass transition temperatures of pharmaceutical amorphous solids,” Aaps Pharmscitech, vol. 21, no. 1, pp. 1–13, 2020. [59] D. G. Papageorgiou, E. Zhuravlev, G. Z. Papageorgiou, D. Bikiaris, K. Chrissafis, and C. Schick, “Kinetics of nucleation and crystallization in poly(butylene succinate) nanocomposites,” Polymer, vol. 55, no. 26, pp. 6725–6734, 2014. [60] M. L. Di Lorenzo, A. Longo, and R. Androsch, “Polyamide 11/poly(butylene succinate) bio-based polymer blends,” Materials, vol. 12, no. 17, p. 2833, 2019. [61] H. Marand, J. Xu, and S. Srinivas, “Determination of the equilibrium melting temperature of polymer crystals: linear and nonlinear Hoffman-Weeks extrapolations,” Macromolecules, vol. 31, no. 23, pp. 8219–8229, 1998. [62] X. Wang, J. Zhou, and L. Li, “Multiple melting behavior of poly(butylene succinate),” European Polymer Journal, vol. 43, no. 8, pp. 3163–3170, 2007. [63] T. Miyata and T. Masuko, “Crystallization behaviour of poly(tetramethylene succinate),” Polymer, vol. 39, no. 6-7, pp. 1399–1404, 1998. [64] S. Chen, C. Ma, and G. Zhang, “Biodegradable polymers for marine antibiofouling: Poly(ε-caprolactone)/poly(butylene succinate) blend as controlled release system of organic antifoulant,” Polymer, vol. 90, pp. 215–221, 2016. [65] F. Lin, D. Wang, and J. Lai, “Asymmetric tpx membranes with high gas flux, ”Journal of Membrane Science, vol. 110, no. 1, pp. 25–36, 1996. [66] Č. Stropnik, V. Musil, and M. Brumen, “Polymeric membrane formation by wet-phase separation; turbidity and shrinkage phenomena as evidence for the elementary processes,” Polymer, vol. 41, no. 26, pp. 9227–9237, 2000. [67] P. Dayal, J. Liu, S. Kumar, and T. Kyu, “Experimental and theoretical investigations of porous structure formation in electrospun fibers,” Macromolecules, vol. 40, no. 21, pp. 7689–7694, 2007. [68] 邱昱維, “濕式靜電紡絲製備聚乳酸纖維型態之研究,” Master’s thesis, National Taiwan University, 2018. [69] S. Khatsee, D. Daranarong, W. Punyodom, and P. Worajittiphon, “Electrospinning polymer blend of PLA and PBAT: Electrospinnability–solubility map and effect of polymer solution parameters toward application as antibiotic-carrier mats,” Journal of Applied Polymer Science, vol. 135, no. 28, p. 46486, 2018. [70] Z. Qiu and W. Yang, “Crystallization kinetics and morphology of poly(butylene succinate)/poly(vinyl phenol) blend,” Polymer, vol. 47, no. 18, pp. 6429–6437, 2006. [71] H. Keith, F. Padden Jr, and R. Vadimsky, “Further studies of intercrystalline links in polyethylene,” Journal of Applied Physics, vol. 37, no. 11, pp. 4027–4034, 1966. [72] B. Kasatkin, V. Grinyuk, and A. Gaidarenko, “Spherulite boundaries and certain aspects of interspherulitic fracture,” Polymer Mechanics, vol. 5, no. 3, pp. 327–332, 1969. [73] H. Teng, Y. Shi, and X. Jin, “Inter-spherulite boundary structure in bulk-crystallized polyethylenes directly observed by atomic force microscopy,” Polymer Journal, vol. 35, no. 5, pp. 436–439, 2003. [74] M. L. Di Lorenzo and M. C. Righetti, “Crystallization-induced formation of rigid amorphous fraction,” Polymer Crystallization, vol. 1, no. 2, p. e10023, 2018.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/85339-
dc.description.abstract聚丁二酸丁二醇酯自1990年晚期開始被學者廣泛研究及討論,為生物可分解高分子。因其可在自然環境下分解成水及二氧化碳,並且越來越多研究提出聚丁二酸丁二醇酯可以完全從生物基原料合成。在當今各國越來越重視環保議題的潮流下,聚丁二酸丁二醇酯市占率在未來五年內預估可以達十五倍的成長。 至今我們可以從文獻找到很多關於聚丁二酸丁二醇酯的降解研究。然而,少有研究針對聚丁二酸丁二醇酯在微結構下的降解機制。從球晶中心和球晶邊界開始降解是目前被大家所接受的觀點。因為觀察降解型態屬於動態的實驗手法,資訊取得的難易度會大大影響實驗的流暢度。 本研究以偏光顯微鏡及原子力顯微鏡作為檢測工具,設計出合適的降解觀察手法。我們將聚丁二酸丁二醇酯製作成薄膜,目的是要降低空間維度易於觀察。然而,根據文獻及實作經驗,顯示出聚丁二酸丁二醇酯相當容易結晶,可長單層球晶的聚丁二酸丁二醇酯不易製作。因此,在實驗前半部分,我們探討了聚丁二酸丁二醇酯的熱性質。並且結合等溫結晶的實驗,我們模擬了聚丁二酸丁二醇酯在各個結晶溫度的球晶成長速率,也預測出低溫區的結晶成長情形。 我們使用旋轉塗佈法製作薄膜。過程中發現溶劑的選用、溶液的濃度和給料的時間點,都會影響薄膜最終的品質。經過調整,我們認為溶劑選用1,1,2,2-四氯乙烷,給料的時間點選擇轉速穩定後再進行,得到的薄膜品質會最好。此外, 2% 的溶液濃度可以製作出能用偏光顯微鏡解析到的厚度,也能順利長出平整的單層球晶薄膜。 從偏光顯微鏡的分析結果,可發現聚丁二酸丁二醇酯薄膜隨著溶液越偏鹼性,則越容易發生降解。原子力顯微鏡也呈現出類似的趨勢。不過,在整個降解實驗,我們並沒有觀察到從球晶中心開始降解的現象。溶液先破壞球晶邊界的連接伸直晶體鏈,再沿著邊界快速破壞薄膜。我們所使用的基板是親水性的玻璃,且聚丁二酸丁二醇酯具有疏水性,因此浸泡在水溶液的環境下會加速破裂的發生。zh_TW
dc.description.abstractPolybutylene succinate(PBS), which has been widely studied and discussed since the late 1990s, was a biodegradable polymer. It can be decomposed into H2O and CO2 in the natural environment, and more and more studies suggest that PBS can be synthesized entirely from bio-based materials. With the increasing emphasis on environmental issues worldwide, the market share of PBS is expected to grow 15 times in the next five years. We can find many studies on the degradation of PBS today. However, the degradation mechanism of microstructure is less studied. The degradation from the center and boundary of the spherulites is widely accepted. Because the degradation morphology is a dynamic observation experiment, the way of obtaining information affects the experimental efficiency. In this study, we used polarized optical microscopy(POM) and atomic force microscopy(AFM) as detection tools and successfully designed a suitable degradation technique. We fabricated PBS thin films to reduce the dimensionality for observation. However, according to literature and our experience, the single-layer spherulite of PBS was hard to manufacture because PBS crystallized quickly. Therefore, we first investigated the thermal properties of PBS. In addition, we simulated the growth rate of spherulites at various crystallization temperatures in combination with isothermal crystallization experiments, and also predicted the crystallization growth in the low-temperature zone. We fabricated our films using spin coating and found that the choice of solvent, the solution's concentration, and the dispensing timing influenced the film's final quality. After optimization, we concluded that the best film was made by dynamic dispense spin coating with 1,1,2,2-tetrachloroethane. In addition, the concentration of 2% PBS could produce a flat film with single-layer spherulites, which could be measured using POM. From the degradation results of POM, we found that the PBS degradability increased with a higher pH value. A similar trend was observed using AFM. However, we did not observe the degradation from the center of the spherulites. The damage started at the spherulite boundary, and then expanded rapidly along the boundary. The glass substrate was hydrophilic and PBS was hydrophobic. Hence the immersion in the aqueous solution would accelerate the rupture rate.en
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dc.description.tableofcontents國立臺灣大學碩士學位論文口試委員會審定書 i 國立臺灣大學學位論文學術倫理暨原創性比對聲明書 ii 致謝 iv 摘要 v Abstract vii Contents ix List of Figures xi List of Tables xiv Chapter 1 Introduction and Literature Reviews 1 1.1 Introduction of biodegradable polymers and poly(butylene succinate) (PBS) 1 1.2 Crystalline structure of PBS 6 1.3 Degradation studies of PBS 10 1.4 Literature reviews on polymer film processes 15 1.4.1 A complete introduction to the spin-coating methodology 15 1.4.2 Polymer crystallization theory 18 Chapter 2 Experiments 25 2.1 Materials 25 2.2 Instruments 27 2.3 Methods 28 2.3.1 PBS purification 28 2.3.2 DSC dynamic heating scan 28 2.3.3 DSC isothermal crystallization analysis 29 2.3.4 Preparation of PBS solutions 29 2.3.5 Glass substrate cleaning 30 2.3.6 Preparation of PBS film by spin-coating 30 2.3.7 Observation on a polarized optical microscope 31 2.3.8 Configuration of alkaline solution 31 2.3.9 Observation on atomic force microscope 32 Chapter 3 Results and Discussions 33 3.1 Characterization of PBS films made by spin-coating methods 33 3.1.1 Thermal property analysis of PBS 34 3.1.2 Film formation by optimized spin-coating technology 39 3.1.3 Growth rates of PBS films with an annealing process 44 3.2 Morphological studies of PBS film degradation 51 3.2.1 Polarized optical microscopy 52 3.2.2 Atomic force microscopy 64 Chapter 4 Conclusions 67 Chapter 5 Future works 69 References 70
dc.language.isoen
dc.subject降解zh_TW
dc.subject旋轉塗佈法zh_TW
dc.subject生物可分解高分子zh_TW
dc.subject球晶zh_TW
dc.subject薄膜zh_TW
dc.subject聚丁二酸丁二醇酯zh_TW
dc.subject結晶動力學zh_TW
dc.subject形態學zh_TW
dc.subjectbiodegradation polymeren
dc.subjectcrystallization kineticsen
dc.subjectmorphologyen
dc.subjectdegradationen
dc.subjectspheruliteen
dc.subjectthin filmen
dc.subjectDynamic dispense spin coatingen
dc.subjectpoly(butylene succinate)en
dc.title旋轉塗佈法製備聚丁二酸丁二醇酯薄膜之結晶型態與降解研究zh_TW
dc.titleMorphology and Degradation Studies on Thin Films of Poly(butylene succinate) with Spin-coating Techniqueen
dc.typeThesis
dc.date.schoolyear110-2
dc.description.degree碩士
dc.contributor.author-orcid0000-0002-1103-4420
dc.contributor.oralexamcommittee童世煌(Shih-Huang Tung),曾勝茂(Sheng-mao Tseng)
dc.subject.keyword旋轉塗佈法,生物可分解高分子,聚丁二酸丁二醇酯,薄膜,球晶,降解,形態學,結晶動力學,zh_TW
dc.subject.keywordDynamic dispense spin coating,biodegradation polymer,poly(butylene succinate),thin film,spherulite,degradation,morphology,crystallization kinetics,en
dc.relation.page80
dc.identifier.doi10.6342/NTU202201604
dc.rights.note同意授權(限校園內公開)
dc.date.accepted2022-07-26
dc.contributor.author-college工學院zh_TW
dc.contributor.author-dept材料科學與工程學研究所zh_TW
dc.date.embargo-lift2022-08-05-
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