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Synthesis and crystallization of blo...

Myers, Sasha B.

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Synthesis and crystallization of block copolymers containing perfectly linear polyethylene.

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	Synthesis and crystallization of block copolymers containing perfectly linear polyethylene./
作者:	Myers, Sasha B.
面頁冊數:	288 p.
附註:	Source: Dissertation Abstracts International, Volume: 69-01, Section: B, page: 0493.
Contained By:	Dissertation Abstracts International69-01B.
標題:	Chemistry, Polymer. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3299840
ISBN:	9780549446903

Synthesis and crystallization of block copolymers containing perfectly linear polyethylene.
Myers, Sasha B.

Synthesis and crystallization of block copolymers containing perfectly linear polyethylene. - 288 p.

Source: Dissertation Abstracts International, Volume: 69-01, Section: B, page: 0493.

Thesis (Ph.D.)--Princeton University, 2008.

Triblocks with LPE endblocks and a rubbery midblock were evaluated as thermoplastic elastomers. Although they showed low tensile strengths, they exhibited high extensibility and good structural recovery from deformation.

ISBN: 9780549446903Subjects--Topical Terms:

1018428
Chemistry, Polymer.

Synthesis and crystallization of block copolymers containing perfectly linear polyethylene.
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100 1 $a Myers, Sasha B. $3 1279870
245 1 0 $a Synthesis and crystallization of block copolymers containing perfectly linear polyethylene.
300 $a 288 p.
500 $a Source: Dissertation Abstracts International, Volume: 69-01, Section: B, page: 0493.
502 $a Thesis (Ph.D.)--Princeton University, 2008.
520 $a Triblocks with LPE endblocks and a rubbery midblock were evaluated as thermoplastic elastomers. Although they showed low tensile strengths, they exhibited high extensibility and good structural recovery from deformation.
520 $a Crystalline block copolymers self-assemble on the nanoscale into a variety of morphologies dependent on block length and type. This thesis describes the synthesis and morphological characterization of several classes of crystalline block copolymers, all containing a linear polyethylene (LPE) block. Defect-free LPE forms thicker, higher-melting crystals with a higher degree of crystallinity compared to its branched counterparts.
520 $a Our synthesis method for LPE involves the ring-opening metathesis polymerization (ROMP) of cyclopentene followed by hydrogenation. We describe the implementation of a Ru-based initiator for ROMP of cyclopentene to produce well-defined polymers (polydispersity<1.2) over a wide range of molecular weight (5-60 kg/mol).
520 $a A new block copolymer synthesis technique was developed by combining Mo-initiated ROMP with anionic polymerization. The ROMP reaction is terminated to yield a styrene-like endgroup, which is subsequently lithiated to act as a macroinitiator from which the anionically-polymerizable block is grown. We employed this method to produce polycyclopentene-polystyrene (PCP-PS) diblocks which became LPE-polyvinylcyclohexane (PVCH) diblocks upon catalytic hydrogenation.
520 $a A series of LPE-PVCH diblocks was used to investigate the crystallization behavior of LPE in confined environments. Because the glass transition temperature of PVCH is higher than the crystallization temperature of LPE, the melt morphology is vitrified upon cooling, confining crystallization within or around the glassy microdomains. Confinement within spherical or cylindrical microdomains directly limits LPE's degree of crystallinity and crystal thickness. Lamellar morphologies impose lesser limitations, because the crystal stems lie parallel to the microdomain interface. Crystals confined within or between cylinders, or within lamellae, show pronounced orientation of their b-axes parallel to the long direction of the microdomain. Confinement can also exert a pronounced influence on the crystallization kinetics.
520 $a Crystalline-crystalline block copolymers of LPE and hydrogenated polynorbornene (hPN), another highly crystalline polymer, were synthesized by ROMP followed by hydrogenation. The block molecular weights determine which block crystallizes first and sets the spherulitic superstructure, within which the second block subsequently crystallizes.
590 $a School code: 0181.
650 4 $a Chemistry, Polymer. $3 1018428
650 4 $a Engineering, Chemical. $3 1018531
650 4 $a Engineering, Materials Science. $3 1017759
690 $a 0495
690 $a 0542
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710 2 $a Princeton University. $3 645579
773 0 $t Dissertation Abstracts International $g 69-01B.
790 $a 0181
791 $a Ph.D.
792 $a 2008
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