Membrane filtration is an important industrial purification process used to access clean and potable water. The fabrication of the membranes used in these purification applications often involves expensive and energy-intensive processes that have a large negative impact on the environment. Sustainable alternatives with a high water flux and strong rejection performance are needed to purify water. The focus of this work is to investigate the use of polymer-grafted cellulose nanocrystals (CNCs) in membrane applications. The impact of the polymer grafting density and polymer conformation was investigated and it is shown that by increasing the grafting density of PEG such that it adopts a semidilute polymer brush conformation, the water flux through the membranes could be increased from 3.5 to 2900 L h–1 m–2 for CNC membranes without and with grafted PEG, respectively. These membranes also exhibited rejection performances with molecular weight cutoffs between 62 and 100 kDa for all polymer-grafted samples, consistent with the ultrafiltration regime. Thus, the design of these one-component composite materials can enhance the water permeability of ultrafiltration membranes while maintaining effective selectivity.
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The effect of polymer grafting on the mechanical properties of PEG ‐grafted cellulose nanocrystals in poly(lactic acid)
Poly(lactic acid) (PLA) is a commercially available bio‐based polymer that is a potential alternative to many commodity petrochemical‐based polymers. However, PLA's thermomechanical properties limit its use in many applications. Incorporating polymer‐grafted cellulose nanocrystals (CNCs) is one potential route to improving these mechanical properties. One key challenge in using these polymer‐grafted nanoparticles is to understand which variables associated with polymer grafting are most important for improving composite properties. In this work, poly(ethylene glycol)‐grafted CNCs are used to study the effects of polymer grafting density and molecular weight on the properties of PLA composites. All CNC nanofillers are found to reinforce PLA above the glass transition temperature, but non‐grafted CNCs and CNCs grafted with short PEG chains (<2 kg mol−1) are found to cause significant embrittlement, generally resulting in less than 3% elongation‐at‐break. By grafting higher molecular weight PEG (10 kg mol−1) onto the CNCs at a grafting density where the polymer chains are predicted to be in the semi‐dilute polymer brush conformation (~0.1 chains nm−2), embrittlement can be avoided.
more » « less- NSF-PAR ID:
- 10385817
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Journal of Polymer Science
- Volume:
- 60
- Issue:
- 24
- ISSN:
- 2642-4150
- Page Range / eLocation ID:
- p. 3318-3330
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Basic Protocol 1 : Tuning viscoelasticity by varying alginate molecular weightBasic Protocol 2 : Tuning viscoelasticity with ionic versus covalent crosslinkingBasic Protocol 3 : Tuning viscoelasticity by adding PEG spacers to alginate chainsSupport Protocol 1 : Testing mechanical properties of alginate hydrogelsSupport Protocol 2 : Conjugating cell‐adhesion peptide RGD to alginate -
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Abstract A versatile synthetic platform is reported that affords high molecular weight graft copolymers containing polydimethylsiloxane (PDMS) backbones and vinyl‐based polymer side chains with excellent control over molecular weight and grafting density. The synthetic approach leverages thiol‐ene click chemistry to attach an atom‐transfer radical polymerization (ATRP) initiator to a variety of commercially available poly(dimethylsiloxane‐
co ‐methylvinylsiloxane) backbones (PDMS‐co ‐PVMS), followed by controlled radical polymerization with a wide scope of vinyl monomers. Selective degradation of the siloxane backbone with tetrabutylammonium fluoride confirmed the controlled nature of side‐chain growth via ATRP, yielding targeted side‐chain lengths for copolymers containing up to 50% grafting density and overall molecular weights in excess of 1 MDa. In addition, by using a mixture of thiols, grafting density and functionality can be further controlled by tuning initiator loading along the backbone. For example, solid‐state fluorescence of the graft copolymers was achieved by incorporating a thiol‐containing fluorophore along the siloxane backbone during the thiol‐ene click reaction. This simple synthetic platform provides facile control over the properties of a wide variety of grafted copolymers containing flexible PDMS backbones and vinyl polymer side chains. -
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Abstract This study demonstrates that protein adsorption on end‐grafted, zwitterionic poly(sulfobetaine) (pSBMA) thin films depends on the grafting density, molecular weight, and ionic strength. Zwitterionic polymers exhibit ultralow nonspecific fouling (protein adsorption) and excellent biocompatibility. This picture contrasts with a recent report that soluble pSBMA chains bind proteins and alter the protein folding stability. To address this apparent contradiction, the dependence of protein adsorption on the chain grafting parameters is investigated: namely, the grafting density, molecular weight, and ionic strength. Studies compared the adsorption of phosphoglycerate kinase and positively charged lysozyme versus the scaled grafting parameter
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