Christopher W Macosko

Dr. Christopher W Macosko


Research Focus & Metrics

Academic Career Length

38Years (1989-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 February 2017 in Science
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JEJames M. Eagan
James M. Eagan
JXJun Xu
Jun Xu
RGRocco DI GIROLAMO
Rocco DI GIROLAMO
CTChristopher M. Thurber
Christopher M. Thurber
CMChristopher W Macosko
Christopher W Macosko
GCGeoffrey W. Coates
Geoffrey W. Coates
How to make opposites compatible: Polyethylene (PE) and isotactic polypropylene ( i PP) are the two most widely used commodity plastics and thus make up a large fraction of the waste stream. However, the two plastics will not mix together, which limits options for dealing with mixed waste and decreases the value of recycled products. Eagan et al. report the synthesis of multiblock copolymers of i PP and PE by using a selective polymer initiator (see the Perspective by Creton). The high-molecular-weig ht blocks could be used to reinforce the interface between i PP and PE and allow blending of the two polymers. Science , this issue p. 814 ; see also p. 797

6 December 2014 in Advanced Functional Materials
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YPYong Tae Park
Yong Tae Park
YQYuqiang Qian
Yuqiang Qian
CCClement Matthew Chan
Clement Matthew Chan
TSTaewon Suh
Taewon Suh
MNMehrdad Ghasemi Nejhad
Mehrdad Ghasemi Nejhad
ASAndreas Stein
Andreas Stein

1 October 2012 in Journal of Pharmaceutical Sciences
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JHJing Han
Jing Han
ZZZhengxi Zhu
Zhengxi Zhu
HQHaitao Qian
Haitao Qian
AWAdam R. Wohl
Adam R. Wohl
CBCharles J. Beaman
Charles J. Beaman
CMChristopher W Macosko
Christopher W Macosko

31 January 2022 in JACS Au
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Journal Article
Open access
JSJeffrey L. Self
Jeffrey L. Self
AZAristotle J. Zervoudakis
Aristotle J. Zervoudakis
XPXiayu Peng
Xiayu Peng
WLWilliam R. Lenart
William R. Lenart
CMChristopher W Macosko
Christopher W Macosko
CEChristopher J. Ellison
Christopher J. Ellison
Properly addressing the global issue of unsustainable plastic waste generation and accumulation will require a confluence of technological breakthroughs on various fronts. Mechanical recycling of plastic waste into polymer blends is one method expected to contribute to a solution. Due to phase separation of individual components, mechanical recycling of mixed polymer waste streams generally results in an unsuitable material with substantially reduced performance. However, when an appropriately designed compatibilizer is used, the recycled blend can have competitive properties to virgin materials. In its current state, polymer blend compatibilization is usually not cost-effective compared to traditional waste management, but further technical development and optimization will be essential for driving future cost competitiveness. Historically, effective compatibilizers have been diblock copolymers or in situ generated graft copolymers, but recent progress shows there is great potential for multiblock copolymer compatibilizers. In this perspective, we lay out recent advances in synthesis and understanding for two types of multiblock copolymers currently being developed as blend compatibilizers: linear and graft. Importantly, studies of appropriately designed copolymers have shown them to efficiently compatibilize model binary blends at concentrations as low as ∼0.2 wt %. These investigations pave the way for studies on more complex (ternary or higher) mixed waste streams that will require novel compatibilizer architectures. Given the progress outlined here, we believe that multiblock copolymers offer a practical and promising solution to help close the loop on plastic waste. While a complete discussion of the implementation of this technology would entail infrastructural, policy, and social developments, they are outside the scope of this perspective which instead focuses on material design considerations and the technical advancements of block copolymer compatibilizers.

1 November 2005 in Journal of Macromolecular Science, Part B
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Closed access
TWTomy Widya
Tomy Widya
CMChristopher W Macosko
Christopher W Macosko
Montmorillonite‐based organoclay was incorporated into rigid polyurethane foams. Clay was dispersed first in the isocyanate component ultrasonically. The dispersion was investigated using small angle X‐ray scattering and rheology. It was found that using toluene as common solvent enhanced dispersion significantly. The addition of 1 wt% clay resulted in reduced cell size from 0.40 to 0.28 mm and increased cell number density on 300‐index foams. Gas chromatography showed that diffusion of blowing agent out of the closed cells of the foam decreased by more than 82% with clay loading. The reduction in permeability is caused by the combined effect of smaller cell size and dispersed nanoclay acting as diffusion barrier. At 1% clay no mechanical strength improvements were observed. Higher levels of clay loading caused significant viscosity increase and a yield stress that made mixing the reactive components difficult.

22 May 2002 in Journal of Polymer Science Part A: Polymer Chemistry
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QLQi‐Wei Lu
Qi‐Wei Lu
THThomas R. Hoye
Thomas R. Hoye
CMChristopher W Macosko
Christopher W Macosko