The aeromagnetic mineralogy of igneous rocks

1979 ◽  
Vol 16 (6) ◽  
pp. 1281-1293 ◽  
Author(s):  
Stephen E. Haggerty

Magnetic minerals in igneous rocks are dominated by phases in the system FeO–Fe2O3–TiO2 and the system Fe–Ni–S. Complex solid solutions within both systems yield divergent magnetic signatures, which are dependent on primary mineralogy, on deuteric cooling, and on post-depositional alteration of the host rock. Intrinsic parameters such as temperature, oxygen fugacity, and sulfur fugacity, have effective buffering capacities, which influence the ratios Fe2+:Fe3+; (Fe2+ + Fe3+):Ti; Fe:S; and (Fe + Ni):S. These ratios are highly sensitive to environmental conditions and correlate with magnetic property measurements. In addition, bulk chemistry plays a major role, and for igneous rocks a striking pattern emerges in which oxygen fugacity is related to SiO2 (i.e., from basic to acid suites) regardless of total pressure. Acidic suites (granites and rhyolites) are more highly oxidized than basic suites (gabbros and basalts); hence. ulvöspinel (Fe2TiO4)-rich and ilmenite (FeTiO3)-rich constituents are characteristic of the latter, whereas magnetite (Fe3O4)-rich and hematite (αFe2O3)-rich components are typical of the former as primary precipitated oxides. Deep-seated equilibration results in exsolution and in low-intensity states of oxidation, and this is in contrast to extrusive suites in which intense states of high temperature oxidation are prevalent. Olivine decomposition in extrusive rocks, and the formation of magnetite solid-solution members in plagioclase and pyroxene in plutonic rocks, yield single domain particles, which in some instances are the dominant magnetic carriers. Sulfide minerals are rare in continental extrusive suites, are more abundant in oceanic basalts and in hypabyssal minor intrusives, and peak in plutonic environments.Within the context of deep crustal magnetic anomalies, and in the determination of Curie isotherms, it is proposed that the primary and secondary mineralogy of plutonic ultramafic rocks be carefully re-evaluated based on current models of serpentinization. Metallic iron and metal alloys of Fe–Ni–Co–Cu are widely recognized in these rock types, and because these minerals have elevated Curie temperatures (620–1100 °C) the depth detection limits of aeromagnetic anomalies need not be constrained by the accepted value of 580 °C, the Curie temperature of magnetite.

2018 ◽  
Vol 21 (7) ◽  
pp. 462-467
Author(s):  
Babak Sadeghi

Aim and Objective: Ultrafine Ag/ZnO nanotetrapods (AZNTP) have been prepared successfully using silver (I)–bis (oxalato) zinc complex and 1, 3-diaminopropane (DAP) with a phase separation system, and have been injected into a diethyl/water solution. Materials and Methods: This crystal structure and lattice constant of the AZNTP obtained were investigated by means of a SEM, XRD, TEM and UV-vis spectrum. Results: The results of the present study demonstrated the growth and characterization AZNTP for humidity sensing and DAP plays a key role in the determination of particle morphology. AZNTP films with 23 nm in arm diameter have shown highly sensitive, quick response sensor material that works at room temperature.


2019 ◽  
Vol 15 (5) ◽  
pp. 505-510
Author(s):  
Yanjuan Zheng ◽  
Qiushi Peng ◽  
Rui Dong ◽  
Tingyu Chen ◽  
Yi Bao ◽  
...  

Introduction: A rapid, and accurate Ultra Performance Liquid Chromatography (UPLC) method was developed to simultaneously analyze Methocarbamol, Paracetamol and the related substances Materials and Methods: Waters ACQUITY UPLC® BEH Phenyl C18 column was used in conjunction with UV detection at 225nm. Gradient elution with 0.05M, pH 6 phosphate buffer and acetonitrile flow at 0.3mL /min rate were used to separate the substances. The retention times for 4-Aminopheno, Paracetamol, Guaifenesin, Methocarbamol, and 4-Chloroacetanilide were 1.319 minute, 2.224 minute, 4.467 minute, 4.769 minute and 5.433 minute respectively. The concentration was linear in the range of 2-100 µg/ml for Methocarbamol, and 1-100 µg/mL for Paracetamol. The percentage recoveries were between 99.28±1.23% to 100.57±0.99% for Methocarbamol, and between 99.08±1.23% to 101.23±1.39% for Paracetamol. Results and Discussion: The validated optimal protocol is robust and accurate for simultaneous analysis of Methocarbamol, Paracetamol and the related substances, applicable for bulk powder as well as pharmaceutical formulation. Conclusion: In this paper, a highly sensitive, accurate, and precise UPLC method with UV-Vis detection was developed and validated for quality control of MET and PAR in bulk as well as in pharmaceutical preparations.


Author(s):  
Lin He ◽  
Peixia Li ◽  
Kai Li ◽  
Tao Lin ◽  
Jin Luo ◽  
...  

A new cross double point discharge (CrossPD) microplasma was designed as an excitation source to construct a miniaturized optical emission spectrometer with hydride generation (HG) for sample introduction. The CrossPD...


2020 ◽  
Vol 18 (1) ◽  
pp. 303-313 ◽  
Author(s):  
Aamir Rasheed ◽  
Tahseen Ghous ◽  
Sumaira Mumtaz ◽  
Muhammad Nadeem Zafar ◽  
Kalsoom Akhter ◽  
...  

AbstractIn the present work, a novel continuous flow system (CFS) is developed for the preconcentration and determination of Cr (VI) using Pseudomonas aeruginosa static biomass immobilized onto an effective and low-cost solid support of powdered eggshells. A mini glass column packed with the immobilized biosorbent is incorporated in a CFS for the preconcentration and determination of Cr (VI) from aqueous solutions. The method is based on preconcentration, washing and elution steps followed by colorimetric detection with 1,5-diphenyl carbazide in sulphuric acid. The effects of several variables such as pH, retention time, flow rate, eluent concentration and loaded volume are studied. Under optimal conditions, the CFS method has a linear range between 10 and 100 μg L-1 and a detection limit of 6.25 μg L-1 for the determination of Cr (VI). The sampling frequency is 10 samples per hour with a preconcentration time of 5 mins. Furthermore, after washing with a 0.1 M buffer (pH 3.0), the activity of the biosorbent is regenerated and remained comparable for more than 200 cycles. Scanning electron microscopy reveals a successful immobilization of biomass on eggshells powder and precipitation of Cr (VI) on the bacterial cell surface. The proposed method proves highly sensitive and could be suitable for the determination of Cr (VI) at an ultra-trace level.


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