In situ generated cellulose nanoparticles to enhance the hydrophobicity of paper

Handsheets with in situ generated cellulose nanoparticles were made from oxidized pulp fibers prepared by 2,2,6,6-tetramethylpiperidinyl-1-oxyl-mediated oxidation of kraft fiber with sodium hypochlorite and sodium bromide. The oxidized pulp fibers were blended prior to handsheet formation for short times (1–3 min). From gravimetric analysis of the supernatant, yield of cellulose nanoparticles generated from this blending process were up to 9.5 dry wt%. Scanning electron microscopy showed that the handsheets fabricated in a wetlay process had increased smoothness with increased blending time. A significant decrease in water vapor transmission rate for the sheets supported the hypothesis that cellulose nanoparticles fill the empty spaces between pulp fibers throughout the handsheet affording a more dense structure. Oxidation significantly enhanced the tensile index of the handsheets and this value was further improved by blending for 2 min. The handsheets were treated with a solution of octadecylamine (ODA) modifying the surface chemistry of the paper. Irreversibly adsorbed ODA on the oxidized cellulose surfaces after extensive extraction was confirmed by Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. Sessile drop contact angle tests for modified handsheets illustrated its enhanced hydrophobicity with contact angles over 90°. Overall the study developed a novel route to make paper with enhanced functionality without the need to separately deposit nanocellulose onto the paper surface.     

An electrochemical immunosensor based on covalent immobilization of okadaic acid onto screen printed carbon electrode via diazotization-coupling reaction

In this work, an electrochemical method based on the diazonium-coupling reaction mechanism for the immobilization of okadaic acid (OA) on screen printed carbon electrode was developed. At first, 4-carboxyphenyl film was grafted by electrochemical reduction of 4-carboxyphenyl diazonium salt, followed by terminal carboxylic group activation by N-hydroxysuccinimide (NHS), N-(3-dimethylaminopropyle)-N′-ethyle-carbodiimide hydrochloride (EDC). Hexamethyldiamine was then covalently bound by one of its terminal amine group to the activated carboxylic group. The carboxyl group of okadaic acid was activated by EDC/NHS and then conjugated to the second terminal amine group on other side of the hexamethyldiamine through amide bond formation. After immobilization of OA, an indirect competitive immunoassay format was employed to detect OA. The immunosensor obtained using this novel approach allowed detection limit of 1.44 ng/L of OA, and was also validated with certified reference mussel samples.     

Thielavin B methyl ester: a cytotoxic benzoate trimer from an unidentified fungus (MSX 55526) from the Order Sordariales

As part of our ongoing investigation of filamentous fungi for anticancer leads, an active fungal extract was identified from the Mycosynthetix library (MSX 55526; from the Order Sordariales). Bioactivity-directed fractionation yielded the known ergosterol peroxide (2) and 5α,8α-epidioxyergosta-6,9(11),22-trien-3β-ol (3), and a new benzoate trimer, termed thielavin B methyl ester (1). The structure elucidation of 1 was facilitated by the use of HRMS coupled to an APPI (atmospheric pressure photoionization) source. Compound 1 proved to be moderately active against a panel of three cancer cell lines.     

Thermal optimization of 1.55 μm OP-VECSEL with hybrid metal–metamorphic mirror for single-mode high power operation

We report on the thermal design and the characterization of InP-based 1.55 μm wavelength large diameter (～100 μm) optically pumped vertical external cavity surface emitting lasers (OP-VECSELs). The device is thermally optimized for high power ( > 70 mW) room-temperature (RT) continuous-wave (CW) single-mode operation. Efficient bottom heat dissipation in the 1/2-VCSEL chip is obtained thanks to the use of a hybrid metal– metamorphic GaAs/AlAs mirror integrated to the InP-based active region, and to subsequent soldering on a SiC substrate. A single-mode output power of 77mW is obtained under CW-RT laser operation, limited by the pump power. Moreover thermal simulations and characterizations of the 1/2-VCSEL chip show that even higher power could be obtained at higher pumping levels, using a CVD diamond substrate.     

A Rapid Quenched‐Flow Device for the Characterisation of the Nascent Polymerisation of Ethylene under Industrial Conditions

Summary: A quenched‐flow reactor is introduced as an effective means for the production of polyolefin particles with precisely controlled reaction times as low as 40 ms. The use of off‐line scanning electron microscopy and induced‐coupled plasma yields experimental data on the development of the kinetics and morphology of nascent structures during the polymerisation of ethylene on a heterogeneous TiCl₄ MgCl₂ Ziegler–Natta catalyst. Initial ex situ observations revealed the development of specific morphologies very early during the reaction (e.g., cracks in platelike surfaces, fines, extrudates, etc.) that can potentially lead to fines, and the kinetic analysis showed extremely high reaction rates at very short times.

Scanning electron micrograph of a network of fibrils formed by the deformation of the surface of a particle due to the generation of internal forces.