Effect of temperature on the conformation and functionality of poly(N-isopropylacrylamide) (PNIPAM)-grafted nanocellulose hydrogels.

HYPOTHESIS: Poly(N-isopropylacrylamide) [PNIPAM]-grafted cellulose nanofibers (CNFs) are new thermo-responsive hydrogels which can be used for a wide range of applications. Currently, there is no clear understanding of the precise mechanism by which CNFs and PNIPAM interact together. Here, we hypothesize that the physical crosslinking of grafted PNIPAM on CNF inhibits the free movement of individual CNF, which increases the gel strength while sustaining its thermo-responsive properties. EXPERIMENTS: The thermo-responsive behaviour of PNIPAM-grafted CNFs (PNIPAM-g-CNFs), synthesized via silver-catalyzed decarboxylative radical polymerization, and PNIPAM-blended CNFs (PNIPAM-b-CNFs) was studied. Small angle neutron scattering (SANS) combined with Ultra-SANS (USANS) revealed the nano to microscale conformation changes of these polymer hybrids as a function of temperature. The effect of temperature on the optical and viscoelastic properties of hydrogels was also investigated. FINDINGS: Grafting PNIPAM from CNFs shifted the lower critical solution temperature (LCST) from 32 °C to 36 °C. Below LCST, the PNIPAM chains in PNIPAM-g-CNF sustain an open conformation and poor interaction with CNF, and exhibit water-like behaviour. At and above LCST, the PNIPAM chains change conformation to entangle and aggregate nearby CNFs. Large voids are formed in solution between the aggregated PNIPAM-CNF walls. In comparison, PNIPAM-b-CNF sustains liquid-like behaviour below LCST. At and above LCST, the blended PNIPAM phase separates from CNF to form large aggregates which do not affect CNF network and thus PNIPAM-b-CNF demonstrates low viscosity. Understanding of temperature-dependent conformation of PNIPAM-g-CNFs engineer thermo-responsive hydrogels for biomedical and functional applications.

Modulating the chiral nematic structure of cellulose nanocrystal suspensions with electrolytes.

HYPOTHESIS: The iridescent optical properties of films made of cellulose nanocrystals (CNC) are controlled by the pitch and range of the chiral nematic structures. These are further tuned with the addition of electrolyte. EXPERIMENTS: Electrolyte type, valency and concentration were varied. The bulk CNC suspension properties were investigated by combining rheology, polarised optical photography and microscopy, while the spacing between crystals was determined using SAXS. FINDINGS: The addition of electrolyte to a CNC suspension containing chiral nematic structures first causes the nematic pitch to increase indicating the suspension has a weaker structure. Further increases in electrolyte concentration cause aggregation and complete breakdown of the chiral nematic structures. The univalent species cause larger changes to the chiral nematic structure with the onset and magnitude of structure breakdown occurring at lower ionic strengths compared with the divalent species. Cation size influences the chiral nematic structure with the order of influence being K+ > Na+ ≈ Ca2+ > Mg2+, which corresponds from the largest to smallest cation. This work demonstrates that both ion valency, concentration and species play a significant role in controlling the chiral nematic structures of CNC suspensions and will be a vital step in the development of CNC liquid crystals, optical materials and sensors.

Self-assembly of cellulose nanocrystals of different lengths.

Hypothesis The self-assembly (SA) of cellulose nanocrystals (CNC) in suspensions is important both from the fundamental and advanced technology development perspective. CNC of different lengths self-assemble differently in suspensions by balancing attractive and repulsive interactions which depends strongly on morphology, surface chemistry and concentrations. Experiments Two different commercial CNC samples (CNC-M and CNC-C) of different lengths were dispersed in Milli-Q water at different concentrations (0.5-10 wt%). CNC-M is provided as a gel at a solid concentration of 10.3 wt% which was diluted in Milli-Q water. CNC-C is sold as a powder which was dispersed in Milli-Q water with a mixer to achieve the desired concentrations. TEM was used to determine morphology of CNC. Polarised optical microscopy is performed to get microscale visualisation of the chiral nematic self-assembly. High flux synchrotron SAXS is applied to evaluate and compare the nanoscale self-assembly mechanisms of CNC of different lengths. Findings The SA of two different types of CNC rods of similar diameter but different lengths is investigated. SAXS analysis shows the short rods in suspension form an isotropic phase (randomly oriented) at lower concentration (0-4 wt%); as concentration is increased, the rods become systematically aligned in a nematic phase. The interrod distance d varies as c-0.33 at the lower concentration, which changes to c-0.5 and even c-1 at the higher concentrations. In contrast, the long rods in suspension remain in the isotropic phase throughout the measured concentration range from 0.5 to 10 wt%. The interrod distance also follows the isotropic power law slope of c-0.33. Suspensions made of the short CNC rods show long range order and large interrod distance compared to those formed by the long rods. POM agrees with the SAXS results. A specific equilibrium between attractive and repulsive forces is required to maintain SA and ordering of the rods. DLVO calculations reveal that the long rods maintain van der Waal attractive force dominating over the electrostatic repulsion, which hinders rods alignment in an ordered manner. However, for the short rods, the weaker attractive interactions are well compensated by the repulsive force which aligns rods in an ordered assembly. This fundamental understanding of the SA of rods in suspensions facilitates the engineering of novel CNC composites of unique optical properties which enables novel applications such as in sensors and bio-diagnostics.

Tailoring the humidity response of cellulose nanocrystal-based films by specific ion effects.

HYPOTHESIS: The optical properties and humidity response of iridescent films made of cellulose nanocrystal (CNC) and polyethylene glycol (PEG) can be tailored by the incorporation of electrolytes chosen based on specific ion effects (SIE). EXPERIMENTS: A series of inorganic salts comprising five different cations and five anions based on the Hofmeister series were mixed with CNC/PEG suspensions, followed by an air-dried process into iridescent solid films. These films were tested in changing relative humidity (RH) environments from 30% to 90% and their photonic properties and mass change monitored. The underlying structures and the mechanism of their formation were quantified in terms of interparticle distance derived from small angle X-ray scattering experiment and pitch size quantified by scanning electron microscope (SEM). FINDINGS: The specific color and color range of CNC/PEG based films are controlled by a specific anion effect achieved by selection of the salt while the specific cation effect is negligible. The salting-in type anions with the same valency result in a red-shift color when films are in the dried state. The salting-in type leads to a greater color changing range during RH changes than the salting-out type. The resultant mass gain/loss trend is consistent with the color change. In contrast, cations do not show any relationships between salting-in effect and the measured properties as observed for anions. The observed SIE can be used to engineer CNC/polymer-based humidity and bio-diagnostic colorimetric indicator devices.

Thermoresponsive Poly(N-isopropylacrylamide) Grafted from Cellulose Nanofibers via Silver-Promoted Decarboxylative Radical Polymerization.

A family of thermoresponsive poly(N-isopropylacrylamide) [PNIPAM]-grafted cellulose nanofibers (CNFs) was synthesized via a novel silver-promoted decarboxylative polymerization approach. This method relies on the oxidative decarboxylation of carboxylic acid groups to initiate free radicals on the surface of CNFs. The polymerization reaction employs relatively mild reaction conditions and can be performed in a one-step, one-pot fashion. This rapid reaction forms a C─C bond between CNF and PNIPAM, along with the formation of free polymer in solution. The degree of functionalization (DF) and the amount of PNIPAM grafted can be controlled by the Ag concentration in the reaction. Similar to native bulk PNIPAM, PNIPAM-grafted CNFs (PNIPAM-g-CNFs) show remarkable thermoresponsive properties, albeit exhibiting a slight hysteresis between the heating and cooling stages. Grafting PNIPAM from CNFs changes its cloud point from about 32 to 36 °C, influenced by the hydrophilic nature of CNFs. Unlike physical blending, covalently tethering PNIPAM transforms the originally inert CNFs into thermosensitive biomaterials. The Ag concentration used does not significantly change the cloud point of PNIPAM-g-CNFs, while the cloud point slightly decreases with fiber concentration. Rheological studies demonstrated the sol-gel transition of PNIPAM-g-CNFs and revealed that the storage modulus (G') above cloud point increases with the amount of PNIPAM grafted. The novel chemistry developed paves the way for the polymerization of any vinyl monomer from the surface of CNFs and carbohydrates. This study validates a novel approach to graft PNIPAM from CNFs for the synthesis of new thermoresponsive and transparent hydrogels for a wide range of applications.

Modulating the chiral nanoarchitecture of cellulose nanocrystals through interaction with salts and polymer.

HYPOTHESIS: The conditions to allow self-assembly of cellulose nanocrystal (CNC) suspensions into chiral nematic structures are based on aspect ratio, surface charge density and a balance between repulsive and attractive forces between CNC particles. EXPERIMENTS: Three types of systems were characterized in suspensions and subsequently in their solid dried films: 1) neat water dialyzed CNC, 2) CNC combined with polyethylene glycol(PEG) (CNC/PEG), and 3) CNC with added salt (CNC/Salt). All suspensions were characterized by polarized optical microscope (POM) and small angle X-ray scattering (SAXS), while the resultant dried films were analyzed by reflectance spectrometer, scanning electron microscope (SEM) and SAXS. FINDINGS: The presence of chiral nematic (CN*) structures was not observed in dialyzed aqueous suspensions of CNC during water evaporation. By introducing salts or a non-adsorbing polymer, chirality was apparent in both suspensions and films. The interaxial angle between CNC rods increased when the suspensions of CNC/PEG and CNC/salt were dried to solid films. The angle was found to be dependent on both species of ions and ionic strength, while the inter-particle distance was only related to the salt concentration, as explained in terms of interaction energies. The CNC suspensions/film chirality can be modulated by controlling the colloidal forces.

Moulding of micropatterned nanocellulose films and their application in fluid handling.

HYPOTHESIS: Well-controlled micropatterned nanocellulose films are able to be fabricated via spray coating onto a micropatterned impermeable moulded surface. The micropattern size is able control the directionality of wicking fluid flow. EXPERIMENTS: Using photolithography and etching techniques, silicon moulds with channel widths of 5-500 µm and depths of 6, 12 and 18 µm were fabricated. Micropatterned nanocellulose sheets were formed by spray coating nanofibre suspensions onto the moulds. We also investigate the effect the dimensions of these micropatterned nanocellulose films have on wicking fluids. FINDINGS: Micropatterns were imparted on the surface of nanocellulose films which resulted in three well-defined regimes of conformation with the moulds: full, partial and no conformation. These regimes were driven by the aspect ratio (channel depth/width) of the moulds. Achieved channel widths and depths were compared to those possible with other micropattern fabrication techniques. The directionality of the wicking water droplets can be controlled with the micropatterned channel. Channels within the full conformation regime resulted in increased directionality of fluid flow compared with those not within this regime. This research demonstrates the industrially scalable process of spray coating has potential to serve as the foundation for a new generation of paper-based microfluidic devices.

Modulating transparency and colour of cellulose nanocrystal composite films by varying polymer molecular weight.

HYPOTHESIS: Cellulose nanocrystals (CNC) can produce photonic composite films that selectively reflect light based on their periodic cholesteric structure. The hypothesis of this research is that by incorporating water-soluble polymer, photonic properties of CNC composite film can be designed by manipulating the polymer molecular weight. EXPERIMENTAL: Flexible free-standing composite films of five different poly (ethylene glycol) (PEG) molecular weights were prepared via air drying under a controlled environment, and characterised by reflectance UV-vis spectrometer, atomic force microscopy (AFM) and scanning electron microscopy (SEM). Films with each molecular weight were investigated over a concentration range. FINDINGS: The colour and transmission haze of the composite films was modified by varying both the PEG molecular weight and concentration. Depending on the molecular weight, the films were able to reflect light from the UV region (242 nm) across the visible spectrum to the near-infrared region (832 nm). Different trends in variation of the reflected light based on the molecular weight was found with increasing PEG concentration and was explained by weak depletion interactions occurring between CNC and PEG, which was reduced with increasing PEG molecular weight.

Grafting Nature-Inspired and Bio-Based Phenolic Esters onto Cellulose Nanocrystals Gives Biomaterials with Photostable Anti-UV Properties.

Invited for this month's cover is the international collaborative work from the Bioresource Processing Research Institute of Australia (BioPRIA)-Monash University and URD Agro-Biotechnologies Industrielles (ABI)-AgroParisTech. The cover image shows how the grafting of Nature-inspired and bio-based phenolic esters on cellulose nanocrystals through click-chemistry provides materials with highly photostable UV-blocking properties. Cover art by David Mendoza. The Full Paper itself is available at 10.1002/cssc.202002017.

An energy efficient production of high moisture barrier nanocellulose/carboxymethyl cellulose films via spray-deposition technique.

Nanocellulose (NC) films are considered as a prospective alternative to non-sustainable packaging materials, however, their higher embodied energy and limited moisture barrier properties are regarded as a huge constraint regarding their commercialization. This study aims to produce films with relatively low environmental impact and improved barrier performance. For this purpose, carboxymethyl cellulose (CMC) and NC were combined, and this resulted in multidimensional advantages. The mass production of films could be achieved in only 2 h (requiring at least 24 h under ambient conditions) when dried in an oven at 75 °C with enhanced mechanical properties and without compromising their dimensional stability. The moisture barrier properties of the NC/CMC films were improved up to 92 % compared with the NC films alone and the results achieved are comparable with packaging materials such as polyethylene terephthalate (PET), polycarbonates (PC) etc. Finally, the NC/CMC (1:1) films have low environmental impact compared with PET films.

Grafting Nature-Inspired and Bio-Based Phenolic Esters onto Cellulose Nanocrystals Gives Biomaterials with Photostable Anti-UV Properties.

New nature-inspired and plant-derived p-hydroxycinnamate esters and p-hydroxycinnamate diesters provide excellent protection against UV radiation when incorporated into a matrix. Herein, an efficient and sustainable pathway is reported to graft these phenolic compounds onto cellulose nanocrystals (CNCs) via click-type copper-catalyzed azide/alkyne cycloaddition (CuAAC) reaction. The successful grafting of the phenolic esters on CNC surface was evidenced by a range of chemical analyses, and the degrees of substitution (DS) of the CNC were found to depend on the structure of the phenolic ester grafted. Moreover, aqueous suspensions of the phenolic ester-grafted CNCs not only strongly absorb in both the UVA and UVB regions, but they also exhibit average to very high photostability. Their wide spectrum UV-absorbing properties and their stability upon exposure to UV are highly influenced by the structure of the phenolic ester, particularly by the extra ester group in p-hydroxycinnamate diesters. These findings demonstrate that cellulose nanocrystals decorated with such plant-derived and nature-inspired phenolic esters are promising sustainable nanomaterials for anti-UV applications.

Controlling the transparency and rheology of nanocellulose gels with the extent of carboxylation.

TEMPO and periodate are combined in a one-shot reaction to oxidise cellulose and produce nanocellulose gels with a wide range of degree of substitution (DS). Highly-oxidised cellulose nanofibres with a high charge of -80 mV were produced. The strong electrical repulsion between TEMPO-periodate oxidised nanofibres (TPOF) results in the formation of well-separated nanofibres with a diameter of 2-4 nm, albeit depolymerised due to high oxidation. TPOF produces highly-transparent gels due to smaller aspect ratio and high surface charge. These properties induce a reduced viscosity and moduli of the gels by decreasing fibre entanglement. TPOF gels are more stable at basic pH and high ionic strength than TEMPO-oxidised gels due to their higher surface charge. Freeze-dried TPOF gels also exhibit remarkable water holding capacity due to enhanced immobilisation of water molecules. The excellent optical properties of the highly transparent gel for red blood cells analysis open new possibilities in diagnostics application.

Reversible pH Responsive Bovine Serum Albumin Hydrogel Sponge Nanolayer.

A pH dependent reversible sponge like behavior of a bovine serum albumin (BSA) nanolayer adsorbed at the gold-saline interface is revealed by quartz crystal microbalance with dissipation (QCM-D), atomic force microscope (AFM) and contact angle measurements. During the saline rinsing cycles, the BSA layer adsorbs water molecules at pH 7.0 and releases them at pH 4.5. The phenomenon remains constant and reproducible upon multiple rinsing cycles. The BSA layer thickness also increases upon rinsing with saline at pH 7.0 and reverses back to its original thickness at pH 4.5. Varying ionic strength with water further desorbs more water molecules from the BSA layer, which decreases its mass and thickness. However, upon both pH and ionic strength changes, all the BSA molecules remain adsorbed irreversibly at the gold interface and only the sorption of water molecules occurs. The study aims at engineering high efficiency pH-responsive biodiagnostics and drug delivery systems.

One-shot TEMPO-periodate oxidation of native cellulose.

TEMPO/NaClO/NaBr and sodium periodate were combined in a one-shot reaction to oxidise cellulose from bleached pulp. Oxidation of cellulose forms two fractions: a highly-carboxylated water-insoluble (up to 1.9 mmol COO-/g, DS = 0.39) and a water-soluble fraction (up to 4 mmol COO-/g, DS = 1.1). Results show that these regioselective oxidants work in synergy to produce fully-oxidised 2,3,6-tricarboxycellulose. Increasing the periodate concentration results in fibrillation and extensive depolymerisation of the pulp cellulose as more residual aldehyde groups participate in the depolymerisation process. X-ray diffraction (XRD) reveals that the addition of periodate increases cellulose crystallinity, retains crystal size but slightly alters the XRD pattern. The degree of substitution (DS), which governs the solubility of carboxylated cellulose, can be controlled by varying the periodate concentration. Combining TEMPO/NaBr/NaClO with sodium periodate simultaneously in a one-shot reaction produces low-cost cellulose with controlled level of carboxylation and unique properties.

Direct AFM force measurements between air bubbles in aqueous monodisperse sodium poly(styrene sulfonate) solutions.

Structural forces play an important role in the rheology, processing and stability of colloidal systems and complex fluids, with polyelectrolytes representing a key class of structuring colloids. Here, we explore the interactions between soft colloids, in the form of air bubbles, in solutions of monodisperse sodium poly(styrene sulfonate) as a model polyelectrolyte. It is found that by self-consistently modelling the force oscillations due to structuring of the polymer chains along with deformation of the bubbles, it is possible to precisely predict the interaction potential between approaching bubbles. In line with polyelectrolyte scaling theory, two distinct regimes of behaviour are seen, corresponding to dilute and semi-dilute polymer solutions. It is also seen that by blending monodisperse systems to give a bidisperse sample, the interaction forces between soft colloids can be controlled with a high degree of precision. At increasing bubble collision velocity, it is revealed that hydrodynamic flow overwhelms oscillatory structural interactions, showing the important disparity between equilibrium behaviour and dynamic interactions.

Direct AFM force measurements between air bubbles in aqueous polydisperse sodium poly(styrene sulfonate) solutions: effect of collision speed, polyelectrolyte concentration and molar mass.

Interactions between colliding air bubbles in aqueous solutions of polydisperse sodium poly(styrene sulfonate) (NaPSS) using direct force measurements were studied. The forces measured with deformable interfaces were shown to be more sensitive to the presence of the polyelectrolytes when compared to similar measurements using rigid interfaces. The experimental factors that were examined were NaPSS concentration, bubble collision velocity and polyelectrolyte molar mass. These measurements were then compared with an analytical model based on polyelectrolyte scaling theory in order to explain the effects of concentration and bubble deformation on the interaction between bubbles. Typically structural forces from the presence of monodisperse polyelectrolyte between interacting surfaces may be expected, however, it was found that the polydispersity in molar mass resulted in the structural forces to be smoothed and only a depletion interaction was able to be measured between interacting bubbles. It was found that an increase in number density of NaPSS molecules resulted in an increase in the magnitude of the depletion interaction. Conversely this interaction was overwhelmed by an increase in the fluid flow in the system at higher bubble collision velocities. Polymer molar mass dispersity plays a significant role in the interactions present between the bubbles and has implications that also affect the polyelectrolyte overlap concentration of the solution. Further understanding of these implications can be expected to play a role in the improvement in operations in such fields as water treatment and mineral processing where polyelectrolytes are used extensively.

Bubble coalescence during acoustic cavitation in aqueous electrolyte solutions.

Bubble coalescence behavior in aqueous electrolyte (MgSO(4), NaCl, KCl, HCl, H(2)SO(4)) solutions exposed to an ultrasound field (213 kHz) has been examined. The extent of coalescence was found to be dependent on electrolyte type and concentration, and could be directly linked to the amount of solubilized gas (He, Ar, air) in solution for the conditions used. No evidence of specific ion effects in acoustic bubble coalescence was found. The results have been compared with several previous coalescence studies on bubbles in aqueous electrolyte and aliphatic alcohol solutions in the absence of an ultrasound field. It is concluded that the impedance of bubble coalescence by electrolytes observed in a number of studies is the result of dynamic processes involving several key steps. First, ions (or more likely, ion-pairs) are required to adsorb at the gas/solution interface, a process that takes longer than 0.5 ms and probably fractions of a second. At a sufficient interfacial loading (estimated to be less than 1-2% monolayer coverage) of the adsorbed species, the hydrodynamic boundary condition at the bubble/solution interface switches from tangentially mobile (with zero shear stress) to tangentially immobile, commensurate with that of a solid-liquid interface. This condition is the result of spatially nonuniform coverage of the surface by solute molecules and the ensuing generation of surface tension gradients. This change reduces the film drainage rate between interacting bubbles, thereby reducing the relative rate of bubble coalescence. We have identified this point of immobilization of tangential interfacial fluid flow with the "critical transition concentration" that has been widely observed for electrolytes and nonelectrolytes. We also present arguments to support the speculation that in aqueous electrolyte solutions the adsorbed surface species responsible for the immobilization of the interface is an ion-pair complex.

Synthesis and fluorescence characterization of MEHPPV oligomers.

Trimer, tetramer, and pentamer oligomers based on the polymer backbone structure of poly[2-methoxy-5-(2'-ethylhexyloxy)-1,4-phenylenevinylene] (MEHPPV) have been synthesized by Horner-Wadsworth-Emmons reactions. The fluorescence spectra, emission quantum yields, and lifetimes of the oligomers have been characterized in dilute chloroform solutions. The oligomers exhibit a sequential increase in absorption and emission wavelength maxima and a decrease in fluorescence lifetime as the π conjugation length is increased. The shortening in excited state lifetime is shown to be due to an increase in the rates of both radiative and nonradiative processes. The absence of a mirror-image relationship for the absorption and fluorescence spectra of the oligomers is attributed to the photoexcitation of a range of torsional configurations followed by relaxation to a more planar arrangement that then emits.