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It is a textbook knowledge that protein photoluminescence stems from the three aromatic amino acid residues of tryptophan(Trp), tyrosine (Tyr), and phenylalanine (Phe), with predominant contributions from Trp. Recently, inspired by the intrinsic emission of nonaromatic amino acids and poly(amino acids) in concentrated solutions and solids, we revisited protein light emission using bovine serum albumin (BSA) as a model. BSA is virtually nonemissive in dilute solutions (≤0.1 mg mL-1 ), but highly luminescent upon concentration or aggregation, showing unique concentration-enhanced emission and aggregation-induced emission (AIE) characteristics. Notably, apart from well-documented UV luminescence, bright blue emission is clearly observed. Furthermore, persistent room-temperature phosphorescence (p-RTP) is achieved even in the amorphous solids under ambient conditions. This visible emission can be rationalized by the clustering-triggered emission (CTE) mechanism. These findings not only provide an in-depth understanding of the emissive properties of proteins, but also hold strong implications for further elucidating the basis of tissue autofluorescence.

The phase behavior of biomolecules containing persistent molecular entities is generally limited due to their characteristic size that exceeds the intermolecular force field. Consequently, favorable properties normally associated with the liquid phase of a substance, such as fluidity or processability, are not relevant for the processing of biomolecules, thus hindering the optimal processing of biomolecules. The implied problem that arises is how to convert folded biomolecules to display a richer phase behavior. To alleviate this dilemma, a generic approach to liquefied polysaccharides-based polymers is proposed, resulting in a polysaccharide fluid with a tunable condensed state structure (solid-gel-liquid). Polysaccharide biobased fluids materials transcend the limits of the physical state of the biobased material itself and can even create completely new properties (different processing methods as well as functions) in a variety of polymeric structures. Considering the solvent incompatible high and low-temperature applications, this method will have a great influence on the design of nanostructures of biomolecular derivatives and is expected to transform biomass materials such as polysaccharide biopolymers from traditional use to resource use, ultimately leading to the efficient use of biomass materials and their sustainability.

Self-reinforcement gel-like halloysite nanotube (g-HNT) hybrids with various viscoelastic behaviors were fabricated by firstly treating with various concentrations of sodium hydroxide (NaOH) solution and then grafting tertiary amine and ion-exchange reacting with sulfonate anions. The morphology, composition, thermal stability and rheological behavior of the g-HNT hybrids were systematically characterized and analyzed using various methods. It is found that the viscoelasticity of g-HNT hybrids can be easily regulated by using different NaOH solution-treated HNTs as inorganic core and temperatures. In addition, the g-HNT hybrids treated with medium concentration of NaOH (0.06 mol L−1) have the lowest viscosity and highest level of dispersion compared with those treated with other concentrations of NaOH solution. Due to the amphiphilic nature of g-HNT hybrids and their lower viscosity than HNT powder, as novel hybrid fillers, they were utilized to prepare polystyrene composites by direct melt blending for achieving simultaneous reinforcement and plasticization effects. Besides the above mentioned advantages, the thermal conductivity of polystyrene composites is also surprisingly improved by reducing the interfacial mismatch between the filler and polymer matrix. The solvent-free and self-reinforcement hybrids provide a convenient and green path for fabricating high-performance polymer composites. © 2017 Society of Chemical Industry

Achieving persistent room-temperature phosphorescence (p-RTP), particularly those of tunable full-colors, from pure organic amorphous polymers is attractive but challenging. Particularly, those with tunable multicolor p-RTP in response to excitation wavelength and time are highly important but both fundamentally and technically underexplored. Here, a facile and general strategy toward color-tunable p-RTP from blue to orange-red based on amidation grafting of luminophores onto sodium alginate (SA) chains, resulting in amorphous polymers with distinct p-RTP and even impressively excitation-dependent and time-dependent afterglows is reported. p-RTP is associated with the unique semi-rigidified SA chains, effective hydrogen bonding network, and oxygen barrier properties of SA, whereas excitation-dependent and time-dependent afterglows should stem from the formation of diversified p-RTP emissive species with comparable but different lifetimes. These results outline a rational strategy toward amorphous smart luminophores with colorful, excitation-dependent, and time-dependent p-RTP, excellent solution processability, and film-forming ability for versatile applications.

A strategy towards efficient mechanochromic luminogens with high contrast is developed. The twisted propeller-like conformations and effective intermolecular interactions not only endow the luminogens with AIE characteristics and high efficiency in the crystalline state, but also render them to undergo conformational planarization and disruption in intermolecular interactions upon mechanical stimuli, resulting in remarkable changes in emission wavelength and efficiency.

The influences of styrene–butadiene–styrene (SBS) copolymer compatibilizer and compounding process on the electrical conduction and thermal stabilities of carbon black (CB)-filled immiscible polypropylene (PP)/polystyrene (PS) (1/1) blends were investigated. The immiscible CB/PP/PS composite with CB homogeneously located in the PS phase exhibited the highest resistivity and the fastest variation amplitudes of electrical resistivity (ρ) and rheological parameters upon annealing. An optimal content of 5 vol% SBS could significantly lower ρ of the composites by partially trapping CB particles in the PP/PS interfacial region and by reducing the phase size. The compatibilizer markedly slowed down the variation amplitudes of ρ and rheological parameters and the phase coalescence of the composites submitted to thermal annealing. The (SBS/CB)/PP/PS composite with CB located at the PP/PS interface and in the PP phase prepared by blending a (SBS/CB) masterbatch with PP and PS exhibited lower ρ and better thermal stability in comparison with the CB/SBS/PP/PS composite with CB mainly within the PS phase and partially at the PP/PS interface prepared by direct blending. Spreading and wetting coefficients were used to explain the CB distribution and the phase morphology of the composites. © 2012 Society of Chemical Industry

Shell-crosslinked core–shell nanoparticles (SCCSNs) were prepared via miniemulsion polymerization of styrene in the presence of silane-modified inorganic silica. The polystyrene (PS) shell of 58.6% in weight fraction was crosslinked using divinylbenzene. SCCSNs were spherical with a diameter distribution from 32 to 98 nm determined by dynamic light scattering. Dynamic rheology of SCCSNs suspended in PS/toluene solution was compared with that of suspensions of naked silica. The critical strain for onset of rheological nonlinearity was independent of SCCSN concentration above a concentration threshold, which differs from the silica suspensions. Linear dynamic rheological investigation revealed that SCCSN suspensions with a PS volume fraction of 20% were fluid-like at low particle concentrations while suspensions containing 4.2 vol% SCCSNs formed a gel-like structure. On the contrary, the silica suspensions with 20.0 vol% PS underwent a fluid-to-solid-like transition with increasing silica concentration. Reasons for the different rheological behaviors of the naked silica and SCCSN suspensions are discussed. Copyright © 2012 Society of Chemical Industry

The electrical and rheological behaviors of carbon black (CB)-filled immiscible polypropylene (PP)/polystyrene (PS) blends were investigated. The compounding sequence influences the phase morphology of the ternary CB/PP/PS composites and the distribution of CB aggregates. Simultaneous measurements of resistance and dynamic modulus were carried out to monitor the phase coalescence of the ternary composites and CB migration and agglomeration in the PS phase during annealing at temperatures above the melting point of PP. The variation of resistivity is mainly attributed to CB agglomeration in the PS phase and the interfacial region, while the variation of dynamic modulus is regarded as the superimposition of the phase coalescence and CB agglomeration in the PS phase. The ternary composites with the majority of CB particles distributed in the interfacial region show the lowest conductive percolation threshold and the most stable resistivity–temperature performance during heating–cooling cycles. Copyright © 2011 Society of Chemical Industry