The aim of this critical review is to provide a broad but digestible overview of mechanochemical synthesis, i.e. reactions conducted by grinding solid reactants together with no or minimal solvent. Although mechanochemistry has historically been a sideline approach to synthesis it may soon move into the mainstream because it is increasingly apparent that it can be practical, and even advantageous, and because of the opportunities it provides for developing more sustainable methods. Concentrating on recent advances, this article covers industrial aspects, inorganic materials, organic synthesis, cocrystallisation, pharmaceutical aspects, metal complexes (including metal–organic frameworks), supramolecular aspects and characterization methods. The historical development, mechanistic aspects, limitations and opportunities are also discussed (314 references).

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Mechanochemistry: opportunities for new and cleaner synthesis

Phase change materials for thermal energy storage

https://www.umsl.edu/~chickosj/JSCPUBS/dsccal.pdf

Reference materials for calorimetry and differential thermal analysis

Ionic Liquids-Based Extraction: A Promising Strategy for theAdvanced Nuclear Fuel Cycle Xiaoqi Sun, Huimin Luo, and Sheng Dai* Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States Energy and Transportation Science Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States Department of Chemistry, University of Tennessee, Knoxville, Tennessee 37916, United States State Key Laboratory of Rare Earth Resource Utilization, Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, P. R. China

Ionic Liquids-Based Extraction: A Promising Strategy for the Advanced Nuclear Fuel Cycle

Microencapsulation of phase change materials (PCMs) is an effective way of enhancing their thermal conductivity and preventing possible interaction with the surrounding and leakage during the melting process, where there is no complete overview of the several methods and techniques for microencapsulation of different kinds of PCMs that leads to microcapsules with different morphology, structure, and thermal properties. In this paper, microencapsulation methods are perused and classified into three categories, i.e. physical, physic-chemical, and chemical methods. It summarizes the techniques used for microencapsulation of PCMs and hence provides a useful tool for the researchers working in this area. Among all the microencapsulation methods, the most common methods described in the literature for the production of microencapsulated phase change materials (MEPCMs) are interfacial polymerization, suspension polymerization, coacervation, emulsion polymerization, and spray drying.

A review of microencapsulation methods of phase change materials (PCMs) as a thermal energy storage (TES) medium

Polyaniline/rare earth oxide composites (PANI/La2O3 and PANI/Sm2O3) were synthesized by in situ polymerization at the presence of sulfosalicylic acid (as dopant). The composites obtained were characterized by Fourier transform infrared spectra (FTIR), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The thermal stability of the composites was investigated by thermogravimetry (TG) and derivative thermogravimetry (DTG). The electrochemical performance of the composites was investigated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The results of FTIR, XRD, SEM, CV, and EIS show that the structure of composite has changed greatly when rare earth oxide content is >0.7 g (PANI/La2O3[w/w(92.7/7.3)] and PANI/Sm2O3[w/w(96.2/3.8)]) and the PANI in the composite has transformed into pernigraniline base (non-conducting state) from emeraldine base (conducting state). TG-DTG analysis indicates that the thermal stability of composite was higher than pure PANI, which is attributed to the interaction between PANI and rare earth oxide.

Thermal stability of several polyaniline/rare earth oxide composites

The decomposition kinetics of the pure polyaniline (PANI), PANI/CeO2 composites, and PANI/Dy2O3 composites were investigated using thermogravimetry (TG) technique under air atmosphere. Two isoconversional methods and multiple linear regression method were used for the evaluation of kinetic parameters from the TG data of different heating rates. The estimation of activation energy values shows that the addition of CeO2 significantly enhances the thermal stability of PANI matrix, while the presence of Dy2O3 slightly reduces the thermal stability of the final composites. The kinetic analysis results show that the kinetic model for the decomposition process for PANI is D3 and for the two kinds of composites is F1–D1.

A kinetic analysis of thermal decomposition of polyaniline and its composites with rare earth oxides

Two chelated orthoborate ionic liquids (ILs), 1-butyl-3-methylimidazolium bis(oxalato)borate ([Bmim][BOB]) and 1-hexyl-3-methylimidazolium bis(oxalato)borate ([Hmim][BOB]), were prepared and characterized. Their thermodynamic properties were studied using adiabatic calorimetry and differential scanning calorimetry (DSC). The thermodynamic properties of the two ILs were evaluated and compared with each other, and then with those of other [Bmim] type ILs. The results clearly indicate that for a given cation (or anion) and at a certain temperature, the more atoms in the anion (or cation), the higher the heat capacity; the higher glass-transition temperatures of [BOB] type ILs than others are mainly caused by the higher symmetry of the orthoborate anion structure. It is suggested that a high content of strong electronegative atoms and C(n) or C(nv) (n = 1,2,3,…,∞) point group symmetry in the anion are favorable for the design and synthesis of room temperature ILs with a wide liquid range.

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Low-temperature heat capacities of 1-alkyl-3-methylimidazolium bis(oxalato)borate ionic liquids and the influence of anion structural characteristics on thermodynamic properties.

Zhi-Cheng Tan

Papers

Thermal stability of several polyaniline/rare earth oxide composites

A kinetic analysis of thermal decomposition of polyaniline and its composites with rare earth oxides

Low-temperature heat capacities of 1-alkyl-3-methylimidazolium bis(oxalato)borate ionic liquids and the influence of anion structural characteristics on thermodynamic properties.

A novel gelling method for stabilization of phase change material Na2HPO4·12H2O with sodium alginate grafted sodium acrylate

Thermochemical study on the properties of polyimide BPADA- m-PDA