FTIR analysis of sulphide mineral surfaces before and after collection: galena

1991 ◽  
Vol 33 (1-4) ◽  
pp. 49-65 ◽  
Author(s):  
J.M. Cases ◽  
P. De Donato
2021 ◽  
Vol 21 (4) ◽  
pp. 1785-1799
Author(s):  
Péter Sipos ◽  
Viktória Kovács Kis ◽  
Réka Balázs ◽  
Adrienn Tóth ◽  
Tibor Németh

Abstract Purpose The close association of Fe-oxyhydroxides and clay minerals might influence the sorption properties of these components. We aimed to study the effect of removing the pedogenic Fe-oxyhydroxides on the sorption of Cd, Cu, Pb, and Zn by the clay mineral particles in soils with contrasting pH. Methods Competitive batch sorption experiments before and after Fe-oxyhydroxide extraction in soils were carried out together with the direct analysis of the metal sorption on individual particles of ferrihydrite, smectite, and illite/smectite by TEM. Results Ferrihydrite was a more effective metal sorbent than clay minerals, although its removal resulted in decreased sorption only for Cd, Cu, and Zn. Ferrhydrite coating blocked metals’ access for certain sorption sites on clay surfaces, which were only accessible for Pb as the most efficient competitor after removing the coating. This observation was the most remarkable for the smectite particles in the alkaline soil. Mineral surfaces sorbed higher Cu than Pb concentrations and higher Zn than Cd concentrations despite the former metals’ lower bulk sorption. Thus, organic surfaces and precipitation contributed to Pb and Cd’s retention to a greater extent than for Cu and Zn. The structural Fe of smectite also promoted the metal sorption in both soils. Conclusion Removal of iron-oxyhydroxide coatings from the soil affects metal sorption selectively. Direct study of metal sorption on individual soil particles enables us to gain a more in-depth insight into soil minerals’ role in this process.


Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3588
Author(s):  
Jiayi Chen ◽  
Yansong Liu ◽  
Jiayue Zhang ◽  
Yuanlin Ren ◽  
Xiaohui Liu

Lyocell fabrics are widely applied in textiles, however, its high flammability increases the risk of fire. Therefore, to resolve the issue, a novel biomass-based flame retardant with phosphorus and nitrogen elements was designed and synthesized by the reaction of arginine with phosphoric acid and urea. It was then grafted onto the lyocell fabric by a dip-dry-cure technique to prepare durable flame-retardant lyocell fabric (FR-lyocell). X-ray photoelectron spectroscopy (XPS) and Fourier-transform infrared spectroscopy (FTIR) analysis demonstrated that the flame retardant was successfully introduced into the lyocell sample. Thermogravimetric (TG) and Raman analyses confirmed that the modified lyocell fabric featured excellent thermal stability and significantly increased char residue. Vertical combustion results indicated that FR-lyocell before and after washing formed a complete and dense char layer. Thermogravimetric Fourier-transform infrared (TG-FTIR) analysis suggested that incombustible substances (such as H2O and CO2) were produced and played a significant fire retarding role in the gas phase. The cone calorimeter test corroborated that the peak of heat release rate (PHRR) and total heat release (THR) declined by 89.4% and 56.4%, respectively. These results indicated that the flame retardancy of the lyocell fabric was observably ameliorated.


2021 ◽  
Author(s):  
Martin Ian Daily ◽  
Mark Duncan Tarn ◽  
Thomas Francis Whale ◽  
Benjamin John Murray

Abstract. Ice-nucleating particles (INPs) are atmospheric aerosol particles that can strongly influence the radiative properties and precipitation onset in mixed-phase clouds by triggering ice formation in supercooled cloud water droplets. The ability to distinguish between INPs of mineral and biological origin in samples collected from the environment is needed to better understand their distribution and sources, but this is challenging. A common method for assessing the relative contributions of mineral and biogenic INPs in samples collected from the environment (e.g., aerosol, rainwater, soil) is to determine the ice-nucleating ability (INA) before and after heating, where heat is expected to denature proteins associated with biological ice nucleants. The key assumption is that the ice nucleation sites of biological origin are denatured by heat, while those associated with mineral surfaces remain unaffected; we test this assumption here. We exposed atmospherically relevant mineral samples to wet heat (INP suspensions warmed to above 90 °C) or dry heat (dry samples heated to 250 °C) and assessed the effects on their immersion mode INA using a droplet freezing assay. K-feldspar, thought to be the dominant mineral-based atmospheric INP type where present, was not significantly affected by wet heating, while quartz, plagioclase feldspars and Arizona test Dust (ATD) lost INA when heated in this mode. We argue that these reductions in INA in the aqueous phase result from direct alteration of the mineral particle surfaces by heat treatment rather than from biological or organic contamination. We hypothesise that degradation of active sites by dissolution of mineral surfaces is the mechanism in all cases due to the correlation between mineral INA deactivation magnitudes and their dissolution rates. Dry heating produced minor but repeatable deactivations in K-feldspar particles but was generally less likely to deactivate minerals compared to wet heating. We also heat tested proteinaceous and non-proteinaceous biogenic INP proxy materials and found that non-proteinaceous samples (cellulose and pollen) were relatively heat resistant. In contrast, the proteinaceous ice-nucleating samples were highly sensitive to wet and dry heat, as expected, although their activity remained non-negligible after heating. We conclude that, while INP heat tests have the potential to produce false positives, i.e., deactivation of a mineral INA that could be misconstrued as the presence of biogenic INPs, they are still a valid method for qualitatively detecting proteinaceous biogenic INP in ambient samples, so long as the mineral-based INA is controlled by K-feldspar.


2020 ◽  
Vol 11 (SPL4) ◽  
pp. 1251-1259
Author(s):  
Madhavan R ◽  
Muthukumar N J ◽  
Savariraj Sagayam C ◽  
Rajalakshmi P ◽  
Brindha P

In Siddha system Arsenics are called as Paasaanam (toxins). Veeram is one of the paasaanam, its chemical formula is Hg2Cl2 (Calomel). Internally arsenic based medicines are used for rheumatoid arthritis, generalized body pain, syphilis, epilepsy and cancer.Various organic agents are used to purify the veeram such as milk, tender coconut, bitter guard and lemon juice. In this study raw veeram and products obtained after purification were analyzed using FTIR Spectroscopy with a view to understand the need and mechanism of this purification processes. FTIR analysis was carried out before and after purification. Efforts were made to study various chemical changes veeram undergoes during this process. FTIR of the raw Veeram and its processed samples were recorded between 4000-400cm-1. In the study raw drug showed only nine functional groups in the region between 3789.36cm-1 and 468.75cm-1. Bitter gourd treated veeram peaks  were observed in the region between 3526.99 and 476.62cm-1 and a total of 13-peaks were obtained.  Milk treated veeram showed peaks in the region between 3851.10 and 470.39cm-1 and total of 16- peaks were obtained. This method indicated presence of large number of functional groups. Lemon juice treated veeram showed peaks in between 3839.33 and 471.99cm-1  total of 15-peaks were obtained. Tender coconut veeram peaks were observed in between 3877.84 and 477.33cm-1  and total of 15-peaks were obtained. From this data number of functional groups increased in purified samples which indicated that the toxic veeram is not only detoxified but also interacted with functional groups of purifying agents there by therapeutic potency is enhanced.


1997 ◽  
Vol 51 (1-4) ◽  
pp. 1-14 ◽  
Author(s):  
D.J. Vaughan ◽  
U. Becker ◽  
K. Wright

Author(s):  
Salaudeen Abdulwasiu Olawale ◽  
Abdulrahman Wosilat Funke ◽  
Aliyu Haruna Dede ◽  
Yakubu Hajara

Thermodynamic and mass balance studies of Pb(II) and Cu(II) biosorption from aqueous solution using chicken feathers (CF) were carried out. Thermodynamic parameters such as standard free energy (ΔG0), enthalpy (ΔH0) and entropy (ΔS0) changes were calculated from the data obtained to predict the nature of adsorption by chicken feathers (CF). From the results, entropy changes were positive indicating an increase in disorderliness in the adsorption of Pb(II) and Cu(II) onto the chicken feathers (CF). The negative values of Gibbs free energy and positive values of enthalpy indicated that the adsorption process by CF was spontaneous and endothermic. Data obtained also showed that the percentage Cu(II) and Pb(II) released by CF after digestion at 25 mg/l were higher than those released at 100 mg/l. Finally, FTIR analysis confirmed the presence of carboxyl, hydroxyl, amino and sulphur containing functional groups on CF, with no substantial variation in the spectra obtained before and after adsorption indicating a possible re use of CF.


1997 ◽  
Vol 51 (1-4) ◽  
pp. 163-170 ◽  
Author(s):  
K. Laajalehto ◽  
I. Kartio ◽  
E. Suoninen

2011 ◽  
Vol 396-398 ◽  
pp. 2388-2393 ◽  
Author(s):  
Hong Mei Deng ◽  
Yong Heng Cheng ◽  
Xiang Yang Chang ◽  
Jian Gong ◽  
Cui Qin Wu ◽  
...  

Cedar sawdust (Cedrus deodara), an agricultural by-product abundant in China, was used as an adsorbent for the removal of Cu(II) from aqueous solutions. The extent of adsorption was investigated as a function of pH, contact time, adsorbate concentration and reaction temperature. The Cu(II) removal was pH-dependent, reaching a maximum at pH 5. The adsorption process followed pseudo-second-order kinetics and equilibrium was reached at 60 min. The rate constantly increased with the increase of temperature, indicating the endothermic nature of adsorption. The equilibrium adsorption capacity of Cu(II) determined from the Langmuir equation was 64.52 mg/g at 25°C. The equilibrium data fitted very well to the Freundlich isotherm model as compared to the Langmuir isotherm. The negative ΔGo values at various temperatures confirm that the adsorption processes are spontaneous. Attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) analysis of cedar sawdust, before and after adsorption of Cu(II), suggested that the main mechanisms involved in the removal of Cu(II) might be the ionic exchange and complexation.


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