Cyclic Poly(phthalaldehyde): Thermoforming a Bulk Transient Material

被引:42
作者
Feinberg, Adam M. [1 ,2 ]
Hernandez, Hector Lopez [1 ,3 ]
Plantz, Christopher L. [1 ,4 ]
Mejia, Edgar B. [1 ,3 ]
Sottos, Nancy R. [1 ,4 ]
White, Scott R. [1 ,5 ]
Moore, Jeffrey S. [1 ,2 ,4 ]
机构
[1] Univ Illinois, Beckman Inst Adv Sci & Technol, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Mech Sci & Engn, Urbana, IL 61801 USA
[4] Univ Illinois, Dept Mat Sci & Engn, Urbana, IL 61801 USA
[5] Univ Illinois, Dept Aerosp Engn, Urbana, IL 61801 USA
关键词
POSITIVE RESIST SYSTEMS; CHEMICAL AMPLIFICATION; AROMATIC-ALDEHYDES; PHTHALALDEHYDE; CYCLOPOLYMERIZATION; POLYMERIZATION; DEGRADATION; MECHANISM;
D O I
10.1021/acsmacrolett.7b00769
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Cyclic poly(phthalaldehyde) (cPPA) is a metastable and stimuli responsive polymer that undergoes rapid solid state depolymerization and has been utilized as a packaging and encapsulating material for transient applications. However, the early onset thermal depolymerization of cPPA severely hinders the fabrication and processing of plastic parts. Herein, the thermally triggered depolymerization of cPPA was investigated and tailored to enable thermal processing and molding of cPPA at moderate temperatures below the thermal depolymerization temperature. Stabilization of cPPA at elevated temperature was accomplished by removal of the latent Lewis acid catalyst BF3 and by addition of radical inhibitors and a Lewis base. Addition of a plasticizer to the stabilized cPPA enabled the fabrication of a monolithic solid polymer via hot press molding. Importantly, it is shown that the thermally processed cPPA retains its stimuli responsive depolymerization capability and will enable future work in the fabrication of bulk plastic parts that depolymerize and disintegrate on demand.
引用
收藏
页码:47 / 52
页数:6
相关论文
共 23 条
[1]   POLYMERIZATION OF AROMATIC ALDEHYDES .3. CYCLOPOLYMERIZATION OF PHTHALALDEHYDE AND STRUCTURE OF POLYMER [J].
ASO, C ;
TAGAMI, S .
MACROMOLECULES, 1969, 2 (04) :414-&
[2]   POLYMERIZATION OF AROMATIC ALDEHYDES .2. CATIONIC CYCLOPOLYMERIZATION OF PHTHALALDEHYDE [J].
ASO, C ;
TAGAMI, S ;
KUNITAKE, T .
JOURNAL OF POLYMER SCIENCE PART A-1-POLYMER CHEMISTRY, 1969, 7 (2PA1) :497-&
[3]  
Diesendruck CE, 2014, NAT CHEM, V6, P624, DOI [10.1038/nchem.1938, 10.1038/NCHEM.1938]
[4]   Reproducible and Scalable Synthesis of End-Cap-Functionalized Depolymerizable Poly(phthalaldehydes) [J].
DiLauro, Anthony M. ;
Robbins, Jessica S. ;
Phillips, Scott T. .
MACROMOLECULES, 2013, 46 (08) :2963-2968
[5]  
Geschke D., 1997, Z F R PHYS CHEMIE, DOI DOI 10.1524/ZPCH.1997.199.PART_1.128
[6]   Phototriggerable, Fully Transient Electronics: Component and Device Fabrication [J].
Gourdin, Gerald ;
Phillips, Oluwadamilola ;
Schwartz, Jared M. ;
Engler, Anthony ;
Kohl, Paul .
2017 IEEE 67TH ELECTRONIC COMPONENTS AND TECHNOLOGY CONFERENCE (ECTC 2017), 2017, :190-196
[7]  
HERNANDEZ H, UNPUB
[8]   Triggered Transience of Metastable Poly(phthalaldehyde) for Transient Electronics [J].
Hernandez, Hector Lopez ;
Kang, Seung-Kyun ;
Lee, Olivia P. ;
Hwang, Suk-Won ;
Kaitz, Joshua A. ;
Inci, Bora ;
Park, Chan Woo ;
Chung, Sangjin ;
Sottos, Nancy R. ;
Moore, Jeffrey S. ;
Rogers, John A. ;
White, Scott R. .
ADVANCED MATERIALS, 2014, 26 (45) :7637-7642
[9]   HIGHLY SENSITIVE THERMALLY DEVELOPABLE POSITIVE RESIST SYSTEMS [J].
ITO, H ;
UEDA, M ;
SCHWALM, R .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY B, 1988, 6 (06) :2259-2263
[10]   CHEMICAL AMPLIFICATION IN THE DESIGN OF DRY DEVELOPING RESIST MATERIALS [J].
ITO, H ;
WILLSON, CG .
POLYMER ENGINEERING AND SCIENCE, 1983, 23 (18) :1012-1018