Engineering Gold Nanotubes with Controlled Length and Near‐Infrared Absorption for Theranostic Applications

Important aspects in engineering gold nanoparticles for theranostic applications include the control of size, optical properties, cytotoxicity, biodistribution, and clearance. In this study, gold nanotubes with controlled length and tunable absorption in the near‐infrared (NIR) region have been exploited for applications as photothermal conversion agents and in vivo photoacoustic imaging contrast agents. A length‐controlled synthesis has been developed to fabricate gold nanotubes (NTs) with well‐defined shape (i.e., inner void and open ends), high crystallinity, and tunable NIR surface plasmon resonance. A coating of poly(sodium 4‐styrenesulfonate) (PSS) endows the nanotubes with colloidal stability and low cytotoxicity. The PSS‐coated Au NTs have the following characteristics: i) cellular uptake by colorectal cancer cells and macrophage cells, ii) photothermal ablation of cancer cells using single wavelength pulse laser irradiation, iii) excellent in vivo photoacoustic signal generation capability and accumulation at the tumor site, iv) hepatobiliary clearance within 72 h postintravenous injection. These results demonstrate that these PSS‐coated Au NTs have the ideal attributes to develop their potential as effective and safe in vivo imaging nanoprobes, photothermal conversion agents, and drug delivery vehicles. To the best of knowledge, this is the first in vitro and in vivo study of gold nanotubes.     

Interaction dynamics of a spherical particle with a suspended liquid film

Hydrodynamics of collision interactions between a particle and gas‐liquid interface such as droplet/film is of keen interest in many engineering applications. The collision interaction between a suspended liquid (water) film of thickness 3.41 ± 0.04 mm and an impacting hydrophilic particle (glass ballotini) of different diameters (1.1–3.0 mm) in low particle impact Weber number ( ) range (1.4–33) is reported. Two distinct outcomes were observed—particle retention in the film at lower Weber number and complete penetration of the film toward higher Weber number cases. A collision parameter was defined based on energy balance approach to demarcate these two interaction regimes which agreed reasonably well with the experimental outcomes. It was shown that the liquid ligament forming in the complete penetration cases breaks up purely by “dripping/end pinch‐off” mechanism and not due to capillary wave instability. An analytical model based on energy balance approach was proposed to determine the liquid mass entrainment associated with the ligament which compared well with the experimental measurements. A good correlation between the %film mass entrained and the particle Bond number ( ) was obtained which indicated a dependency of Bo^1.72. Computationally, a three‐dimensional CFD model was developed to simulate these interactions using different contact angle boundary conditions which in general showed reasonable agreement with experiment but also indicated deficiency of a constant contact angle value to depict the interaction physics in entirety. The computed force profiles from computational fluid dynamics (CFD) model suggest dominance of the pressure force over the viscous force almost by an order of magnitude in all the Weber number cases studied. © 2015 American Institute of Chemical Engineers AIChE J, 62: 295–314, 2016     

Bio-derived sodium silicate for the manufacture of alkali-activated binders: Use of bamboo leaf ash as silicate source

Alkali activated binders are a promising alternative to the use of Portland cement in the manufacture of concrete for curbing CO₂ emissions. Novel sources of silicates have been investigated in recent years for reducing cost and environmental impacts associated with the use of chemical activators. This study describes the production of solid sodium silicate (SS) activating powder from bamboo leaf ash (BLA). Bamboo leaves were calcined at 550–800°C, mixed with NaOH pellets, and heated in an oven at 300°C. The obtained silicate powder was used for activating blended fly ash/slag samples. Mechanical and microstructural properties of BLA-based samples were compared to those of samples made with commercially available chemicals. The strength of BLA-activated mortars matched the commercially-sourced activators, being 25–30 MPa at 7 days and exceeding 40 MPa at 28 days. The microstructural analysis suggested that BLA-based SS showed a lesser degree of dissolution of precursors at 7 days, but the quality of the matrix was higher than that of NaOH-activated samples. These results confirmed that the reactivity of BLA-silicate powder was similar to that of commercial SS solutions, and show the potential valorization of future biomass renewable waste in the production of low carbon, alkali-activated concretes.     

Phase‐shifting differential interference contrast microscope with Savart shear prism and rotatable analyser

A novel differential interference contrast microscope (DICM) is proposed in this research. It is constituted by inserting a Savart shear prism between the objective and sample of a polarising microscope having a rotatable analyser as the phase‐shifter, and it is with the ability to enhance image contrast using the principle of shearing interferometry. This letter is to introduce the configuration, interpret the interference patterns and present the experimental setup of the DICM. In addition, this letter is to display the experimental results from the uses of the setup; the results demonstrate the validity and ability of the DICM.     

An Investigation of Starch/Surfactant Interactions Using Viscosimetry and Differential Scanning Calorimetry

Viscosity measurements at 60°C and differential scanning calorimetry were used to investigate the behaviour of starch/surfactant mixtures. Preparation temperature proved to dramatically modify the rheological effects observed with wheat starch and the amylose-complexing emulsifiers but was a less important variable with the more hydrophilic detergent species examined. The latter also caused quite large viscosity enhancements with waxy maize starch, effects not observed, or expected, with the emulsifiers. When 0.2-M sodium chloride was present, however, the derergents were found to behave like the emulsifiers. To account for these differences it is suggested that the detergent species are able to complex with amylopectin molecules as well as with amylose, unlike the emulsifiers which, as previously thought, only seem to complex with amylose. Calorimetry experiments did not give direct evidence, in terms of observable transitions, for the occurence of amylopectin/surfactant complexes with any of the examined surfactants. Analysis of the enthalpies associated with the several transitions observed however did provide substantial support for the suggested hypothesis.     

The Effect of Solutes on the Gelatinization Temperature Range of Potato Starch

The gelatinization behaviour of potato starch in an excess of water or solutions of sugars, other organic hydroxy compounds, or various inorganic salts was studied. The distribution of water and solutes between the external phase and the starch granules was measured by refractometry and a dye exclusion technique. When the limited water uptake of native starch granules is taken into account, the cooperative nature of gelatinization and the effect of water content on gelatinization behaviour can be explained solely on the basis of the Flory theory of polymer melting. Following the same argument, the effect of many solutes can be approximately described by the derived relationship between initial gelatinization temperature, water activity of the system and volume fraction of water in the granules.     

Diffusion of water into a photopolymer film

Sorption of water vapor into thin films of a crosslinked dimethacrylate UV-cured polymer was measured by means of a quartz crystal microbalance apparatus. The diffusion coefficient and solubility were obtained. An upper limit to the water vapor diffusion coefficient, namely, the diffusion coefficient for liquid water in intimate contact with the sample, was measured for reference purposes by both gravimetric and infrared spectral techniques. A water uptake value for thick films was obtained gravimetrically as a reference for the thin film value. Measurement of the diffusion coefficient allows the determination of the length of time that the photopolymer could act as an effective water vapor barrier.     

Phase equilibria studies in the CaO–SiO2–Al2O3–MgO system with CaO/SiO2 ratio of 0.9

Phase equilibria and liquidus temperatures in the CaO–SiO₂–Al₂O₃–MgO system at a CaO/SiO₂ weight ratio of 0.9 in the liquid phase have been experimentally determined employing high-temperature equilibration and quenching technique followed by electron probe X-ray microanalysis. Isotherms at 1573, 1623, 1673, and 1773 K were determined and the primary phase fields of wollastonite, melilite, olivine, periclase, spinel, and corundum have been located. Compositions of the olivine and melilite solid solutions were analyzed and discussed. Comparisons between the newly constructed diagram, existing data, and FactSage predicted phase diagrams were performed and differences were discussed. The present study will be useful for guidance of industrial practices and further development of thermodynamic modeling.