Thermal behavior of Sr-form of gordaite

Cation-exchanged Sr-form of gordaite was successfully obtained from Ca-form of gordaite by an ion-exchange reaction. Data of XRD, SEM-EDS and DTA-TG-MS were used to characterize the Sr-form. Thermal decomposition of Sr-gordaite was studied for the first time in regards of thermal events and mass loss during volatile releasing. It was found similarity with Sr-gordaite and Ca-gordaite in terms of processes, type, and amount of volatiles released, but also some differences were found concerning the temperature correspondence of the volatiles evolving and the type of thermal decomposition products. The influence of the exchangeable cations (Na, Ca, or Sr) on the dehydration of the interlayer in the gordaite type structure were also established.

[NiEn3](MoO4)0.5(WO4)0.5 Co-Crystals as Single-Source Precursors for Ternary Refractory Ni–Mo–W Alloys

The co-crystallisation of [NiEn3](NO3)2 (En = ethylenediamine) with Na2MoO4 and Na2WO4 from a water solution results in the formation of [NiEn3](MoO4)0.5(WO4)0.5 co-crystals. According to the X-ray diffraction analysis of eight single crystals, the parameters of the hexagonal unit cell (space group P–31c, Z = 2) vary in the following intervals: a = 9.2332(3)–9.2566(6); c = 9.9512(12)–9.9753(7) Å with the Mo/W ratio changing from 0.513(3)/0.487(3) to 0.078(4)/0.895(9). The thermal decomposition of [NiEn3](MoO4)0.5(WO4)0.5 individual crystals obtained by co-crystallisation was performed in He and H2 atmospheres. The ex situ X-ray study of thermal decomposition products shows the formation of nanocrystalline refractory alloys and carbide composites containing ternary Ni–Mo–W phases. The formation of carbon–nitride phases at certain stages of heating up to 1000 °C were shown.

Odor Recognition of Thermal Decomposition Products of Electric Cables Using Odor Sensing Arrays

An odor sensing system with chemosensitive resistors was used to identify the gases generated from overheated cables to prevent fire. Three different electric cables for a distribution cabinet were used. The cables had an insulation layer made of polyvinyl chloride (PVC) or cross-linked polyethylene (XLPE). The heat resistance of the cables was tested by differential thermal and thermogravimetric analyses. The thermal decomposition products of the cables were investigated by gas chromatography-mass spectrometry (GC-MS). For the odor sensing system, two types of 16-channel array were used to detect the generated gases. One contains high-polarity GC stationary phase materials and the other contains GC stationary phase materials of high to low polarity. The system could distinguish among three cable samples at 270 °C with an accuracy of about 75% through both arrays trained with machine learning. Furthermore, the system could achieve a recall rate of 90% and a precision rate of 70% when the abnormal temperature was set above the cables’ allowable conductor temperature at 130 °C. The odor sensing system could effectively detect the abnormal heating of the cables before the occurrence of fire. Therefore, it is helpful for fire prediction and detection systems in factories and substations.

Structural and Thermal Investigations of Co(II) and Ni(II) Coordination Polymers Based on biphenyl-4,4′-dioxydiacetate Linker

Two coordination polymers, [Co(µ4-L)(H2O)2]n (1) and [Ni(µ-L)(H2O)4]n (2), were solvothermally assembled from the corresponding metal(II) chlorides and biphenyl-4,4-dioxydiacetic acid (H2L) as a flexible dicarboxylate linker. The cobalt(II) compound 1 featured a layer-pillared 3D metal-organic network with a cds topology, while the nickel(II) derivative 2 represented a linear chain 1D coordination polymer with a 2C1 topology. The µ4− and µ-L2− linkers exhibited different denticity and coordination modes in the synthesized compounds, thus contributing to their structural diversity. The dimensionality of 1 and 2 had an influence on their thermal stability and decomposition processes, which were investigated in detail by TG-DSC and TG-FTIR methods. Thermal decomposition products of coordination polymers were also analyzed by PXRD, confirming the formation of Co3O4/CoO and NiO as final materials. The obtained compounds broaden a family of coordination polymers assembled from flexible dicarboxylate linkers.

Sintering of Mg and its Alloys under Hydrogen Atmospheres

Ongoing investigations have highlighted that MIM of Mg shows high potential for mass production of small lightweight components as well as of degradable implants with complex geometry. However, prior research activities have shown that Mg reacts sensitively to atmosphere impurities like oxygen and specific thermal decomposition products of the used backbone polymers. Polyethylene based polymers reveal a negative influence on sintering of Mg while polypropylene based polymers behave uncritically. This work is highlighting that when hydrogen instead of argon atmosphere is used during sintering, the negative influence caused by carbon residuals at the particle boundaries can be prevented. Mg-0.9Ca elongation increased with a slight decrease in UTS revealing a strengthening effect of the carbon residuals at the particle boundaries. For pure Mg UTS could be increased from 7 MPa up to 80 MPa with elongation of 6% showing the positive effect of hydrogen on the sintering of Mg.

Magnetic sorption materials for recovery of organic anions from aqueous solutions

Layered double hydroxides (LDHs) belong to the class of two-dimensional anionic clays with a layered structure similar to brucite. The combination of sorption and magnetic properties of layered materials is promising. In this work, magnetic materials based on LDHs (MLDHs) were synthesized and their sorption and magnetic properties were studied. The synthesis of LDHs was carried out by a co-precipitation method followed by calcination. Intercalated Mg, Fe(III)-, Mg, Fe(III), Al-and Mg, Al-LDHs were prepared using LDHs by rehydration in solutions of iron(III) citrate (Cit) or oxalate (Ox) followed by the calcination at 400°C for 2-4 h. LDHs and their thermal decomposition products were characterized by FTIR spectroscopy, laser and X-ray diffraction and thermogravimetry. The sorption experiment was carried out under static conditions using glutamic acid (Glu) as a model organic compound. The maximum sorption capacity of Mg, Fe(III)-LDH and Mg, Al-FeCit-LDH calcined at 400°C was 6.6 and 8.8 mg/g Glu, respectively. The sorption kinetics of intercalated and calcined Mg, Al-and Mg, Fe(III), Al-LDH and calcined at 500º C Mg, Fe(III)-LDH was described by the pseudo-second order model. The magnetic properties of the LDHs and thermal decomposition products were retained after the adsorption of glutamic acid, making it possible to easily separate these MLDHs from the solution by magnetic field.