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SBIR Phase I: Versatile Biobased Plastics from Omega-hydroxylated fatty acids

SBIR Phase I: Versatile Biobased Plastics from Omega-hydroxylated fatty acids
SBIR 第一阶段:由 Omega 羟基化脂肪酸制成的多功能生物基塑料
批准号:
1141949
负责人:
Jiali Cai
金额:
$15.0万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-01-01 至 2012-06-30

项目摘要

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中文摘要
翻译
这个小企业创新研究第一阶段项目将创建一个含有omega-羟基脂肪酸(omega-HOFAs)重复单元的生物塑料家族,以填补商用生物塑料的空白。首先,阐明omega-HOFA链长对相应聚合物(P[omega-HOFA])材料性能的影响。然后,将研究反应共混方法,以产生既利用聚乳酸(PLA)强度又利用P(ω - hofa)延展性的生物塑料。将改变共混工艺参数(如时间、温度、催化剂和催化剂浓度)以调整P(ω - hofa)/PLA的酯交换反应,这将导致“微调”。相相容性及共混物物理力学性能的优化。我们预计,相对于PLA, P(omega-HOFA)/PLA共混物将显著提高水解稳定性、抗冲击性和抗翘曲性。将建立反应器配置和相应工艺变量的要求,作为P(omega-HOFA)合成和反应性混合的功能尺度。进一步测定P(ω - hofas)和P(ω - hofas)/PLA的可堆肥性。第一阶段研究计划的成功完成将导致对材料热学和物理机械性能的全面分析,这是确定商业应用所需的,并进一步吸引战略工业合作伙伴。该项目的更广泛的影响/商业潜力是开发新的生物基材料,满足消费者不断变化的需求,同时提供比现有产品更高的性价比。目前许多生物塑料都存在固有的问题,限制了它们的市场渗透。与该计划特别相关的是PLA,由于其脆性行为,不充分的蒸气传输性能,水解不稳定性和低冲击强度,阻碍了其潜在的使用。我们的omega- hofa为塑料行业提供了一种通用的、易于再生的基础材料,通过均聚、共聚和共混,可用于生产各种具有理想物理和机械性能的生物塑料。对P(omega-HOFAs)与PLA共混物的初步研究表明,PLA的许多缺陷,如其脆性行为,都被消除了,而共混物的强度相对于P(omega-HOFAs)有了重要的提高。这项工作将侧重于获得这些共混材料的物理力学性能的基本信息,因为酯交换的程度是通过反应共混来控制的。此外,还将了解混合如何影响两种组分的生物降解性。这项工作的结果将是可再生的可生物降解塑料,其性能优于石油衍生的竞争对手,并减少我们对石油化工生产的依赖。
英文摘要
This Small Business Innovation Research Phase I project will create a family of bioplastics containing omega-hydroxyfatty acid (omega-HOFAs) repeat units to fill a gap in commercially available bioplastics. First, the effects of omega-HOFA chain length on corresponding polymer (P[omega-HOFA]) material properties will be elucidated. Then, reactive blending methods will be studied to generate bioplastics that exploit both polylactic acid (PLA) strength and P(omega-HOFA) ductility. Blend process parameters (e.g. time, temperature, catalyst, and catalyst concentration) will be varied to adjust P(omega-HOFA)/PLA transesterification which will result in ?fine-tuning? of phase compatibility and optimization of blend physical-mechanical properties. We anticipate that, relative to PLA, P(omega-HOFA)/PLA blends will have significantly improved hydrolytic stability, impact resistance, and warp resistance. Requirements will be established for reactor configuration and corresponding process variables as a function scale for both P(omega-HOFA) synthesis and reactive blending. Furthermore, the compostability of P(omega-HOFAs) and P(omega-HOFAs)/PLA will be determined. Successful completion of the proposed Phase I research program will result in a thorough analysis of material thermal and physico-mechanical properties needed for identification of commercial applications and to further engage strategic industrial partners. The broader impact/commercial potential of this project is to develop new biobased materials that meet evolving needs of consumers while providing cost-performance advantages over existing products. Many current bioplastics have inherent problems that limit their market penetration. Of particular relevance to this program is PLA that is hindered in its potential use due to its brittle behavior, inadequate vapor transmission properties, hydrolytic instability, and low impact strength. Our omega-HOFAs provide a versatile readily renewable building block to the plastics industry that through homopolymerization, copolymerization and blending can be used to produce a wide-range of bioplastics with desired physical and mechanical properties. Preliminary work on blends of P(omega-HOFAs) with PLA show that many deficiencies of PLA, such as its brittle behavior, are eliminated while blends show important improvements in strength relative to P(omega-HOFAs). This work will focus on gaining fundamental information on the physical-mechanical properties of these blend materials as the degree of transesterification is manipulated by reactive blending. Furthermore, an understanding will be gained on how blending effects the biodegradability of both components. The outcome of this work will be renewable biodegradable plastics that out-perform their petroleum derived competitors and decrease our dependency on petroleum for chemical production.
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