語系:
繁體中文
English
說明(常見問題)
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
Programmable Deformation of Liquid Crystal Elastomers.
紀錄類型:
書目-語言資料,手稿 : Monograph/item
正題名/作者:
Programmable Deformation of Liquid Crystal Elastomers./
作者:
Fowler, Hayden.
面頁冊數:
1 online resource (174 pages)
附註:
Source: Dissertations Abstracts International, Volume: 85-06, Section: B.
Contained By:
Dissertations Abstracts International85-06B.
標題:
Physical chemistry. -
電子資源:
click for full text (PQDT)
ISBN:
9798381163339
Programmable Deformation of Liquid Crystal Elastomers.
Fowler, Hayden.
Programmable Deformation of Liquid Crystal Elastomers.
- 1 online resource (174 pages)
Source: Dissertations Abstracts International, Volume: 85-06, Section: B.
Thesis (Ph.D.)--University of Colorado at Boulder, 2023.
Includes bibliographical references
This thesis investigates the programmable deformation of liquid crystal elastomers (LCEs) for directional electromechanical actuation and omnidirectional localized stretch. Focus is placed on developing LCEs for these functionalities through materials chemistry, processing, and properties adjustments. Through these adjustments, this work explores enhancing directional electromechanical deformation by improving the appropriate material properties (i.e., mechanical and dielectric) and enabling localization of deformation to omnidirectional stretch via processing of unaligned LCEs. The first part of this thesis primarily focuses on enhancing the magnitude, speed, and recovery of directional electromechanical deformation in LCEs. To this end, the first aim develops LCEs prepared from thiol-acrylate photopolymerizations with high Young's modulus contrast, low Young's modulus perpendicular to the alignment direction, and relatively high dielectric constant. The resulting materials accomplish uniaxial strains of up to 17.5% at 3.5 kV, demonstrating a marked improvement. Furthermore, LCEs respond and recover quickly, making them fully responsive to 1 Hz cycling frequency. The ability to align LCEs to photopatterned surfaces enables +1 azimuthal defect orientation, generating cone deformations on exposure to voltage. To further enhance deformation, the second aim prepares LCEs from thiol-ene photopolymerizations with tunable crosslinking. The first part of this aim explores the amenability of surface-enforced alignment and variation of crosslinker concentration to adjust material properties. Thiol-ene photopolymerization results in rapid network conversion, and materials are surface alignable, retaining the cybotactic nematic phase. While thermal and mechanical properties can be adjusted via crosslinking, decreasing crosslinker concentration results in the loss of Young's modulus contrast. LCEs are also explored for their thermomechanical response to investigate the role of cybotactic nematic phase behavior. In the second part of this aim, LCEs are prepared with an additional allyl ether functionalized liquid crystalline monomer while maintaining moderate crosslinker concentration. This coincidentally results in improved mechanical and dielectric properties, enhancing the directional electromechanical deformation. LCEs accomplish uniaxial strains of 28% at 4 kV and show improved speeds of deformation and recovery. As a result, residual strain accumulation over multiple cycles is significantly reduced.The second part of this thesis focuses on enabling localized deformations to omnidirectional stretch in LCEs via processing. To do this, the third and final aim prepares LCEs from thiol-acrylate photopolymerizations without macroscopic alignment (polydomain). By crosslinking in the precursor's isotropic or nematic state (referred to as isotropic and nematic genesis, respectively), the mechanical properties of LCEs are differentiated. A mask is used to pattern adjacent regions of isotropic or nematic genesis on a monolithic material, enabling patterning of mechanical properties without directionality. The resulting LCEs localize strain to the softer, isotropic genesis regions on deformation. Furthermore, the lack of directionality in the mechanical properties enables localization of omnidirectional stretch. Strain localization is predicted well by finite elements analysis simulations.
Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2024
Mode of access: World Wide Web
ISBN: 9798381163339Subjects--Topical Terms:
1148725
Physical chemistry.
Subjects--Index Terms:
Liquid crystal elastomersIndex Terms--Genre/Form:
554714
Electronic books.
Programmable Deformation of Liquid Crystal Elastomers.
LDR
:04842ntm a22004097 4500
001
1148339
005
20240924101857.5
006
m o d
007
cr bn ---uuuuu
008
250605s2023 xx obm 000 0 eng d
020
$a
9798381163339
035
$a
(MiAaPQ)AAI30812471
035
$a
AAI30812471
040
$a
MiAaPQ
$b
eng
$c
MiAaPQ
$d
NTU
100
1
$a
Fowler, Hayden.
$3
1474285
245
1 0
$a
Programmable Deformation of Liquid Crystal Elastomers.
264
0
$c
2023
300
$a
1 online resource (174 pages)
336
$a
text
$b
txt
$2
rdacontent
337
$a
computer
$b
c
$2
rdamedia
338
$a
online resource
$b
cr
$2
rdacarrier
500
$a
Source: Dissertations Abstracts International, Volume: 85-06, Section: B.
500
$a
Advisor: White, Timothy J.
502
$a
Thesis (Ph.D.)--University of Colorado at Boulder, 2023.
504
$a
Includes bibliographical references
520
$a
This thesis investigates the programmable deformation of liquid crystal elastomers (LCEs) for directional electromechanical actuation and omnidirectional localized stretch. Focus is placed on developing LCEs for these functionalities through materials chemistry, processing, and properties adjustments. Through these adjustments, this work explores enhancing directional electromechanical deformation by improving the appropriate material properties (i.e., mechanical and dielectric) and enabling localization of deformation to omnidirectional stretch via processing of unaligned LCEs. The first part of this thesis primarily focuses on enhancing the magnitude, speed, and recovery of directional electromechanical deformation in LCEs. To this end, the first aim develops LCEs prepared from thiol-acrylate photopolymerizations with high Young's modulus contrast, low Young's modulus perpendicular to the alignment direction, and relatively high dielectric constant. The resulting materials accomplish uniaxial strains of up to 17.5% at 3.5 kV, demonstrating a marked improvement. Furthermore, LCEs respond and recover quickly, making them fully responsive to 1 Hz cycling frequency. The ability to align LCEs to photopatterned surfaces enables +1 azimuthal defect orientation, generating cone deformations on exposure to voltage. To further enhance deformation, the second aim prepares LCEs from thiol-ene photopolymerizations with tunable crosslinking. The first part of this aim explores the amenability of surface-enforced alignment and variation of crosslinker concentration to adjust material properties. Thiol-ene photopolymerization results in rapid network conversion, and materials are surface alignable, retaining the cybotactic nematic phase. While thermal and mechanical properties can be adjusted via crosslinking, decreasing crosslinker concentration results in the loss of Young's modulus contrast. LCEs are also explored for their thermomechanical response to investigate the role of cybotactic nematic phase behavior. In the second part of this aim, LCEs are prepared with an additional allyl ether functionalized liquid crystalline monomer while maintaining moderate crosslinker concentration. This coincidentally results in improved mechanical and dielectric properties, enhancing the directional electromechanical deformation. LCEs accomplish uniaxial strains of 28% at 4 kV and show improved speeds of deformation and recovery. As a result, residual strain accumulation over multiple cycles is significantly reduced.The second part of this thesis focuses on enabling localized deformations to omnidirectional stretch in LCEs via processing. To do this, the third and final aim prepares LCEs from thiol-acrylate photopolymerizations without macroscopic alignment (polydomain). By crosslinking in the precursor's isotropic or nematic state (referred to as isotropic and nematic genesis, respectively), the mechanical properties of LCEs are differentiated. A mask is used to pattern adjacent regions of isotropic or nematic genesis on a monolithic material, enabling patterning of mechanical properties without directionality. The resulting LCEs localize strain to the softer, isotropic genesis regions on deformation. Furthermore, the lack of directionality in the mechanical properties enables localization of omnidirectional stretch. Strain localization is predicted well by finite elements analysis simulations.
533
$a
Electronic reproduction.
$b
Ann Arbor, Mich. :
$c
ProQuest,
$d
2024
538
$a
Mode of access: World Wide Web
650
4
$a
Physical chemistry.
$3
1148725
650
4
$a
Analytical chemistry.
$3
1182118
650
4
$a
Materials science.
$3
557839
650
4
$a
Chemical engineering.
$3
555952
653
$a
Liquid crystal elastomers
653
$a
Deformation
653
$a
Electromechanical actuation
653
$a
Strain localization
653
$a
Dielectric properties
655
7
$a
Electronic books.
$2
local
$3
554714
690
$a
0542
690
$a
0794
690
$a
0486
690
$a
0494
710
2
$a
University of Colorado at Boulder.
$b
Chemical and Biological Engineering.
$3
1241260
710
2
$a
ProQuest Information and Learning Co.
$3
1178819
773
0
$t
Dissertations Abstracts International
$g
85-06B.
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=30812471
$z
click for full text (PQDT)
筆 0 讀者評論
多媒體
評論
新增評論
分享你的心得
Export
取書館別
處理中
...
變更密碼[密碼必須為2種組合(英文和數字)及長度為10碼以上]
登入