Abstract:Microcrystals of diaquocobalt(II) oxalate have been synthesized by the coprecipitation reaction of aqueous solutions of Cobalt (II) bromide and oxalic acid. Chemical analysis and thermal experiments revealed that there is only one phase present. X-ray powder diffraction studies show that this compound is orthorhombic with space group Cccm. Molar susceptibility versus temperature measurements show the existence of an antiferromagnetic ordering, however, the hysteresis measured in magnetization measurements as a… Show more
“…To better elucidate the thermal behaviour of the complexes, a graph of the weight difference for consecutive rows against the temperature was plotted (Figure 7). The thermograms of four of the complexes (MC 2 O 4 ⋅ H 2 O, where M = Fe 2+ , Co 2+ , Ni 2+ , and Zn 2+ ) show two well defined steps of weight loss in agreement with reports in literature [24,28,31]. The first weight loss for FeC 2 O 4 ⋅ H 2 O (20.9%) occurs in the range 170-218 ∘ C. This is attributed to the elimination of two molecules of water of crystallization according to the theoretical value (19.69%).…”
Section: X-ray Diffractionsupporting
confidence: 89%
“…The XRD spectra of the cobalt complexes synthesised at different temperatures are shown in Figure 4. The observed XRD patterns are similar to that of the standard prepared from commercial oxalic acid as well as to those reported in the literature [20,24]. This indicates that cobalt oxalate dihydrate was obtained at the different synthesis temperatures.…”
Section: X-ray Diffractionsupporting
confidence: 87%
“…The two bands at 1359 and 1314 cm −1 are those of C-O symmetric stretching mode. The difference between ] as (COO) and ] sym (COO) stretching frequencies is 255 cm −1 indicating a bidentate or a terminal monodentate coordination mode of the oxalate ligand in the complexes[24]. The bands at 822 cm −1 is attributed to the bending vibration of O-C-O and the band at 745 cm −1 (absent in the spectrum of the Cu complex) is attributed to H-O-H rocking.…”
A green, simple, and environmentally benign synthetic approach has been utilised to obtain some bivalent metal oxalates from Averrhoa carambola juice extract, without any purification or special treatment of the juice. The main acid components (oxalic acid and ascorbic acid) of the juice were identified by HPLC technique. The effect of temperature on the purity of the product has been investigated. The as-synthesized metal oxalates were thermally decomposed at low temperatures to their respective metal oxide nanoparticles. The metal oxalates and their respective thermal decomposition products were characterized by Fourier Transform Infrared spectroscopy, X-ray diffraction analysis, and thermogravimetry.
“…To better elucidate the thermal behaviour of the complexes, a graph of the weight difference for consecutive rows against the temperature was plotted (Figure 7). The thermograms of four of the complexes (MC 2 O 4 ⋅ H 2 O, where M = Fe 2+ , Co 2+ , Ni 2+ , and Zn 2+ ) show two well defined steps of weight loss in agreement with reports in literature [24,28,31]. The first weight loss for FeC 2 O 4 ⋅ H 2 O (20.9%) occurs in the range 170-218 ∘ C. This is attributed to the elimination of two molecules of water of crystallization according to the theoretical value (19.69%).…”
Section: X-ray Diffractionsupporting
confidence: 89%
“…The XRD spectra of the cobalt complexes synthesised at different temperatures are shown in Figure 4. The observed XRD patterns are similar to that of the standard prepared from commercial oxalic acid as well as to those reported in the literature [20,24]. This indicates that cobalt oxalate dihydrate was obtained at the different synthesis temperatures.…”
Section: X-ray Diffractionsupporting
confidence: 87%
“…The two bands at 1359 and 1314 cm −1 are those of C-O symmetric stretching mode. The difference between ] as (COO) and ] sym (COO) stretching frequencies is 255 cm −1 indicating a bidentate or a terminal monodentate coordination mode of the oxalate ligand in the complexes[24]. The bands at 822 cm −1 is attributed to the bending vibration of O-C-O and the band at 745 cm −1 (absent in the spectrum of the Cu complex) is attributed to H-O-H rocking.…”
A green, simple, and environmentally benign synthetic approach has been utilised to obtain some bivalent metal oxalates from Averrhoa carambola juice extract, without any purification or special treatment of the juice. The main acid components (oxalic acid and ascorbic acid) of the juice were identified by HPLC technique. The effect of temperature on the purity of the product has been investigated. The as-synthesized metal oxalates were thermally decomposed at low temperatures to their respective metal oxide nanoparticles. The metal oxalates and their respective thermal decomposition products were characterized by Fourier Transform Infrared spectroscopy, X-ray diffraction analysis, and thermogravimetry.
“…The % extraction values calculated using the ICP-OES analysis results of the solutions taken from the reactor at the end of the 3 hours experiment period are given in Table 3. When Table 3 [29]. The EDS analysis of the solid material includes the peaks of cobalt and oxygen.…”
In this study, roasted spent Co-Mo/Al2O3 hydrodesulfurization (HDS) catalyst was dissolved in oxalic acid (H2C2O4) solution and optimum conditions were determined for obtaining cobalt oxalate dihydrate (CoC2O4∙2H2O). The thermal decomposition behavior of the obtained CoC2O4∙2H2O was investigated by TG/DTG-DTA analysis. The characterization of CoC2O4∙2H2O was carried out by XRD, FT-IR and SEM-EDS analytical techniques. Optimum conditions for the production of CoC2O4∙2H2O were determined as 25 oC temperature, 0.25 M H2C2O4 concentration, 1/20 g mL-1 solid/liquid ratio and 300 rpm stirring speed. CoC2O4∙2H2O was obtained with a reaction yield of 90.9 %. TG/DTG-DTA analysis carried out in dry air atmosphere showed that CoC2O4∙2H2O decomposed in two steps. In the first step that occurs between 118-196 oC temperatures, CoC2O4∙2H2O is dehydrated. In the second step, which occurs between 248-279 oC temperatures, it was determined that metallic cobalt was formed first, and then metallic cobalt was oxidized and converted into Co3O4 compound because it was performed in the air atmosphere.
“…This uncompensated antiferromagnetism produces weak ferromagnetism (WF). Recently, investigations in the quasi-onedimensional magnetic compound β − CoC 2 O 4 · 2H 2 O [6] revealed that the intra and interchain magnetic interactions tilt the spins, distorting the antiferromagnetic order and producing the WF.…”
Microcrystals of orthorhombic nickel (II) oxalate dihydrate were synthesized through a precipitation reaction of aqueous solutions of nickel chloride and oxalic acid. Magnetic susceptibility exhibits a sharp peak at 3.3 K and a broad rounded maximum near 43 K. We associated the lower maximum with a metamagnetic transition that occurs when the magnetic field is about ≥3.5 T. The maximum at 43 K is typical of 1D antiferromagnets, whereas weak ferromagnetism behavior was observed in the range of 3.3–43 K.
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