Bio-Based Bisbenzoxazines with Flame Retardant Linker

This work explores the strategy of incorporating a highly substituted reactive flame retardant into a benzoxazine moiety. For this purpose, a DOPO-based flame retardant received a chain extension via reaction with ethylene carbonate. It was then reacted with phloretic acid to obtain a diphenol end-capped molecule, and further reacted with furfurylamine and paraformaldehyde to obtain a benzoxazine monomer via a Mannich-like ring closure reaction. This four-step synthesis yielded a partly bio-based halogen-free flame retardant benzoxazine monomer (DOPO-PA-fa). The successful synthesis was proven via NMR, IR and MS analysis. The polymerization behavior was monitored by DSC and rheological analysis both showing the polymerization starts at 200 °C to yield pDOPO-PA-fa. pDOPO-PA-fa has a significant thermal stability with a residual mass of 30% at 800 °C under ambient atmosphere. Furthermore, it reached a V-0 rating against small flames and an OI of 35%. Blended with other benzoxazines, it significantly improves their thermal stability and fire resistance. It emphasizes its potential as flame retardant agent.

Fabricating Na/In/C Composite Anode with Natrophilic Na–In Alloy Enables Superior Na Ion Deposition in the EC/PC Electrolyte

In conventional ethylene carbonate (EC)/propylene carbonate (PC) electrolyte, sodium metal reacts spontaneously and deleteriously with solvent molecules. This significantly limits the practical feasibility of high-voltage sodium metal batteries based on Na metal chemistry. Herein, we present a sodium metal alloy strategy via introducing NaIn and Na2In phases in a Na/In/C composite, aiming at boosting Na ion deposition stability in the common EC/PC electrolyte. Symmetric cells with Na/In/C electrodes achieve an impressive long-term cycling capability at 1 mA cm−2 (> 870 h) and 5 mA cm−2 (> 560 h), respectively, with a capacity of 1 mAh cm−2. In situ optical microscopy clearly unravels a stable Na ion dynamic deposition process on the Na/In/C composite electrode surface, attributing to a dendrite-free and smooth morphology. Furthermore, theoretical simulations reveal intrinsic mechanism for the reversible Na ion deposition behavior with the composite Na/In/C electrode. Upon pairing with a high-voltage NaVPOF cathode, Na/In/C anode illustrates a better suitability in SMBs. This work promises an alternative alloying strategy for enhancing Na metal interfacial stability in the common EC/PC electrolyte for their future applications.

Flash C-H Chlorination of Ethylene Carbonate Using a New Photoflow Setup

We report flash C-H chlorination of ethylene carbonate, which gives chloroethylene carbonate, a precursor to ethylene carbonate. A novel photoflow setup designed for a gas-liquid biphasic reaction turned out to be useful for the direct use of chlorine gas in flow. The setup employed sloped channels so as to make the liquid phase thinner, ensuring high surface to volume ratio. When ethylene carbonate was introduced to the reactor, the residence time was measured to be 15 or 30 sec, depending on the slope of the reactor to be 15 or 5 °C, respectively. Such short time exposition sufficed the photo C-H chlorination. The partial irradiation of the flow channels sufficed for the C-H chlorination, which is consistent with the requirement of photoirradiation for the purpose of radical initiation. We also found that the contaminated water negatively influenced the performance of C-H chlorination. The 100% selectivity for single chlorination required the low conversion of ethylene carbonate such as 9%, which was controlled by limited introduction of chlorine gas. At a higher conversion of ethylene carbonate such as 63%, the selectivity for mono-chlorinated ethylene carbonate over di-chlorinated ethylene carbonate was 86%. We found that the contaminated water negatively influenced the performance of the C-H chlorination.

Study FTIR and AC Conductivity of Nanocomposite Electrolytes

In the present work polymer electrolytes were formulated using the solvent casting technique. Under special conditions, the electrolyte content was of fixed ratio of polyvinylpyrolidone (PVP): polyacrylonitrile (PAN) (25:75), ethylene carbonate (EC) and propylene carbonate (PC) (1:1) with 10% of potassium iodide (KI) and iodine I2 = 10% by weight of KI. The conductivity was increased with the addition of ZnO nanoparticles. It is also increased with the temperature increase within the range (293 to 343 K). The conductivity reaches maximum value of about (0.0296 S.cm-1) with (0.25 g) ZnO. The results of FTIR for blend electrolytes indicated a significant degree of interaction between the polymer blend (PVP and PAN) and the KI salt. From the electrolyte observations of the nanocomposites, the broad peak became narrower after adding the ZnO nanoparticle to the KI salt. The dielectric reaction decreased with the increase of the frequency at room temperature. The high dielectric permittivity of the polymer at lower frequencies can be attributed to the dipoles having sufficient time to get aligned with the electric field, resulting in higher polarization.