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1. Sustainability and Adhesive Performance of Plant Oil-Based Latexes

   Iryna Bon, Vasylyna Kirianchuk ( June 2021 , Great Lakes Regional Meeting (GLRM) 2021)

   Sustainability of the adhesives prepared from fossil-based materials has become a growing concern. Thus, replacement of petroleum-based materials by ones derived from renewable resources is pursued as a sustainable strategy for reducing their carbon footprint. Biobased latexes can be widely used as waterborne adhesives if their performance and properties are competitive to those currently available in the market. This work aims to evaluate the performance of latex adhesives with higher biobased content recently developed in our group. For this purpose, plant oil-based vinyl monomers HOSBM and CMM (derived from high oleic soybean oil and camelina oil, respectively) in combination with methyl methacrylate (MMA) and butyl acrylate (BA) were copolymerized using miniemulsion to yield latexes to be tested as adhesives. The MMA (“rigid” fragment) content was kept at 55 wt%, while BA (within remaining 45 wt% of the “soft” fragments) has been gradually replaced by either CMM or HOSBM. The effect of partial substitution of the BA by CMM or HOSBM on adhesive properties was assessed using peel testing (ASTM D 1876-08) on the multiple substrates. Presence of plant oil-based fragments in latex copolymers improves adhesives peel strength on most substrates. Plant oil-based latexes with the maximum content of CMM or HOSBM (up to 45wt %) and their optimal adhesive performance were determined on various carpet and paperboard substrates. Additionally, Life Cycle Assessment (LCA) method was used as a tool to evaluate the environmental performance of the synthesized latex adhesives as well as identify the hotspots in the synthesis of these plant-derived adhesives in their early design stages. LCA of plant oil-based monomers can explain to which extent the sustainability of the biobased latex adhesives can be improved. The authors thank the NSF Industry and University Cooperative Research Center for Bioplastic and Biocomposites for financial support. Thanks to NSF CB2 (1916564) 

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2. Sustainable glucose-based block copolymers exhibit elastomeric and adhesive behavior

   https://doi.org/10.1039/c6py00700g  

   Nasiri, Mohammadreza ; Reineke, Theresa M. ( January 2016 , Polymer Chemistry)

   Herein, we present the direct modification of glucose, an abundant and inexpensive sugar molecule, to produce new sustainable and functional polymers. Glucose-6-acrylate-1,2,3,4-tetraacetate (GATA) has been synthesized and shown to provide a useful glassy component for developing an innovative family of elastomeric and adhesive materials. A series of diblock and triblock copolymers of GATA and n -butyl acrylate (n-BA) were created via Reversible Addition–Fragmentation Chain Transfer (RAFT) polymerization. Initially, poly(GATA)- b -poly(n-BA) copolymers were prepared using 4-cyano-4-[(ethylsulfanylthiocarbonyl)sulfanyl] pentanoic acid (CEP) as a chain transfer agent (CTA). These diblock copolymers demonstrated decomposition temperatures of 275 °C or greater and two glass transition temperatures ( T g ) around −45 °C and 100 °C corresponding to the PnBA and PGATA domains, respectively, as measured by differential scanning calorimetry (DSC). Triblock copolymers of GATA and n-BA, with moderate dispersities ( Đ = 1.15–1.29), were successfully synthesized when S , S -dibenzyl trithiocarbonate (DTC) was employed as the CTA. Poly(GATA)- b -poly(nBA)- b -poly(GATA) copolymers with 14–58 wt% GATA were prepared and demonstrated excellent thermomechanical properties ( T d ≥ 279 °C). Two well-separated glass transitions near the values for homopolymers of n-BA and GATA (∼−45 °C and ∼100 °C, respectively) were measured by DSC. The triblock with 14% GATA exhibited peel adhesion of 2.31 N cm −1 (when mixed with 30 wt% tackifier) that is superior to many commercial pressure sensitive adhesives (PSAs). Use of 3,5-bis(2-dodecylthiocarbonothioylthio-1oxopropoxy)benzoic acid (BTCBA) as the CTA provided a more efficient route to copolymerize GATA and n-BA. Using BTCBA, poly(GATA)- b -poly(nBA)- b -poly(GATA) triblock copolymers containing 12–25 wt% GATA, with very narrow molar mass distributions ( Đ ≤ 1.08), were prepared. The latter series of triblock copolymers showed excellent thermal stability with T d ≥ 275 °C. Only the T g for the PnBA block was observed by DSC (∼−45 °C), however, phase-separation was confirmed by small-angle X-ray scattering (SAXS) for all of these triblock copolymers. The mechanical behavior of the polymers was investigated by tensile experiments and the triblock with 25% GATA content demonstrated moderate elastomeric properties, 573 kPa stress at break and 171% elongation. This study introduces a new family of glucose-based ABA-type copolymers and demonstrates functionality of a glucose-based feedstock for developing green polymeric materials. 

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3. Zwitterionic copolymer additive architecture affects membrane performance: fouling resistance and surface rearrangement in saline solutions

   https://doi.org/10.1039/C8TA11553B  

   Kaner, Papatya ; Dudchenko, Alexander V. ; Mauter, Meagan S. ; Asatekin, Ayse ( February 2019 , Journal of Materials Chemistry A)

   Membrane separations are simple to operate, scalable, versatile, and energy efficient, but their broader use is curtailed by fouling or performance decline due to feed component depositing on the membrane surface. Surface functionalization with groups such as zwitterions can mitigate the adsorption of organic compounds, thus limiting fouling. This can be achieved by using surface-segregating copolymer additives during membrane manufacture, but there is a need for better understanding of how the polymer structure and architecture affect the effectiveness of these additives in improving membrane performance. In this study, we aim to explore the impact of the architecture of zwitterionic copolymer additives for polyvinylidene fluoride (PVDF)-based membranes in fouling mitigation and ionic strength response. We prepared membranes from blends of PVDF with zwitterionic (ZI) copolymers with two different architectures, random and comb-shaped. As the random copolymer, we used poly(methyl methacrylate- random- sulfobetaine-2-vinyl pyridine) (PMMA- r -SB2VP) synthesized by free radical polymerization. The comb-shaped copolymer was synthesized by grafting SB2VP side-chains from a PVDF backbone by controlled radical polymerization. Membranes were fabricated from PVDF-copolymer blends containing up to 5 wt% ZI copolymer. Compared to the additive-free PVDF membrane, water permeance increased five-fold with 5 wt% addition of either copolymer. The comb copolymer additive led to better resistance to fouling by a saline oil-in-water emulsion and to simulated protein adsorption in Atomic Force Microscopy (AFM) force measurements. The additive architecture had a significant influence on how membranes respond to changes in feed salinity, which is known to affect intra- and inter-molecular interactions in zwitterionic polymers. The random copolymer containing membrane showed a small and mostly reversible decrease in its permeance with salinity. In contrast, the comb copolymer-containing membrane underwent a conformational reorganization in saline solutions that leads to an irreversible permeance decrease, increased zwitterionic group content on the membrane surface, and smoother surface topography. The higher mobility of the zwitterionic groups in the comb-shaped architecture facilitates reorganization of the zwitterionic side-chains in response to ionic strength. Overall, this study establishes a new approach for developing highly fouling resistant membranes and defines how the architecture of a zwitterionic copolymer additive impacts the ionic strength response and fouling resistance of the membrane. 

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4. Electrically Accelerated Self‐Healable Polyionic Liquid Copolymers

   https://doi.org/10.1002/smll.202201952  

   Liu, Qianhui ; Wang, Siyang ; Zhao, Zeyu ; Tong, Jianhua ; Urban, Marek W. ( May 2022 , Small)

   Electrically accelerated self‐healable poly(ionic liquids) copolymers that exhibit resistor‐capacitor (RC) circuit properties are developed. At low alternating current (AC) frequencies these materials behave as a resistor (R), whereas at higher frequencies as a capacitor (C). These properties are attributed to a combination of dipolar and electrostatic interactions in (1‐[(2‐methacryloyloxy)ethyl]‐3‐butylimidazolium bis(trifluoromethyl‐sulfonyl)imide) copolymerized with methyl methacrylate (MMA) monomers to form p(MEBIm‐TSFI/MMA)] copolymers. When the monomer molar ratio (MEBIm‐TSFI:MMA) is 40/60, these copolymers are capable of undergoing multiple damage‐repair cycles and self‐healing is accelerated by the application of alternating 1.0–4.0 V electric field (EF). Self‐healing in the absence of EFs is facilitated by van der Waals (vdW) interactions, but the application of AC EF induces back and forth movement of charges against the opposing force that result in dithering of electrostatic dipoles giving rise to interchain physical crosslinks. Electrostatic inter‐ and intrachain interactions facilitated by copolymerization of ionic liquid monomers with typically dielectric acrylic‐based monomers result in enhanced cohesive energy densities that accelerate the recovery of vdW forces facilitating self‐healing. Incorporating ionic liquids into commodity polymers offers promising uses as green conducting solid polyelectrolytes in self‐healable energy storage, energy‐harvesting devices, and many other applications.

    

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5. Allyl Sulfides in Garlic Oil Initiate the Formation of Renewable Adhesives

   https://doi.org/10.1039/D3PY00390F  

   Sayer, Kyler B. ; Miller, Veronica L. ; Merrill, Zackery ; Davis, Anthony E. ; Jenkins, Courtney L. ( January 2023 , Polymer Chemistry)

   The development of inverse vulcanization has provided a simple method to create sulfur-based materials. The low cost, ease of synthesis, and variety of applications has led to a rapid expansion of the field. These polysulfides can be synthesized with a wide range of sulfur contents (20-90% S) depending on the desired properties. Garlic essential oil (GEO) has a high sulfur content, which offers the opportunity to replace sulfur, a petroleum byproduct, with a renewable monomer to make materials with moderate sulfur contents. Using a one-pot, solvent-free synthesis, comparable to inverse vulcanization, GEO can be polymerized to create renewable adhesives at temperatures as low as 120 °C with reaction times decreasing at higher temperatures. Here we have explored the composition of garlic oil from a variety of commercial suppliers by NMR. Through simple 1H NMR analysis, the major sulfur-containing compounds of GEO can be identified and differentiated by sulfur rank. These data were used to select garlic oils with varied compositions to examine the impact on the poly(GEO) properties using solubility, gel permeation chromatography, differential scanning calorimetry, and thermogravimetric analysis as well as adhesive performance. GEO was then subjected to different reaction times and temperatures and the degree of polymerization was monitored by 1H NMR. The polysulfides were then evaluated as adhesives at different extents of polymerization to better understand how the reaction conditions impact adhesive performance. The failure mode and mechanical properties of the polymers were analyzed using measurements of maximum adhesion strength and work of adhesion. This study has provided a better understanding of polymers formed from GEO, providing a viable route to developing renewable, S-based materials. 

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