A REVIEW OF SOME COMMONLY USED PARAMETERS FOR THE DETERMINATION OF OIL POLLUTION

1977 ◽  
Vol 1977 (1) ◽  
pp. 487-491
Author(s):  
Michael Gruenfeld and ◽  
Uwe Frank

ABSTRACT A state-of-the-art review is provided describing specific parameters of petroleum oils that are used by various investigators to demonstrate the presence of oil pollution in water, sediments, and biological tissues. Several representative publications are discussed with regard to the techniques used for distinguishing between petroleum hydrocarbons and organics that are of recent biological origin. The techniques include chromatographic procedures using alumina and silica gel for separating hydrocarbons from other organics, followed by instrumental methods such as gas chromatography, fluorescence spectroscopy, ultraviolet absorption spectroscopy, et al. The various oil parameters that are used to demonstrate the presence of petroleum oils are discussed, and the most effective ones are recommended. In addition, a recent study is also described in which several of the parameters were used to demonstrate the presence of oil pollution in sediments from a mangrove swamp in Puerto Rico.

2021 ◽  
Vol 11 (12) ◽  
pp. 5493
Author(s):  
Andrzej Gawor ◽  
Andrii Tupys ◽  
Anna Ruszczyńska ◽  
Ewa Bulska

Nowadays growing attention is paid to the control of fluorine content in samples of biological origin as it is present in the form of various biologically active organic compounds. Due to the chemically-rich matrix of biological tissues, the determination of fluorine becomes a very difficult task. Furthermore, a required complex sample preparation procedure makes the determination of the low contents of F by ion chromatography UV-Vis or ion-selective electrodes not possible. High-resolution continuum source graphite furnace molecular absorption spectrometry (HR-CS GF MAS) seems to be the best option for this purpose due to its high robustness to matrix interferences, especially in the presence of carefully selected modifiers. In this work the possibility of quantitative F determination in water and animal tissues was examined by measuring the molecular absorption of gallium monofluoride (GaF) at 211.248 nm with the use of a commercially available HR-CS GF MAS system. Experimental conditions for the sensitive and precise determination of fluorine were optimized, including the time/temperature program as well as addition of gallium and modifier mixture in combined mode. Under these conditions the fluoride present in the sample was stabilized up to 600 °C, and the optimum vaporization temperature for GaF was 1540 °C. Palladium and zirconium deposited onto the graphite surface served as solid modifiers; sodium acetate and ruthenium modifiers were added directly to the sample. The limit of detection and the characteristic mass of the method were 0.43 μg/L and 8.7 pg, respectively. The proposed procedure was validated by the use of certified reference materials (CRMs) of lake water and animal tissue; the acceptable recovery was obtained, proving that it can be applied for samples with a similar matrix.


2019 ◽  
Vol 96 (10) ◽  
pp. 929-933 ◽  
Author(s):  
Nikolay V. Rusakov ◽  
M. A. Vodyanova ◽  
N. Yu. Starodubova ◽  
L. G. Donerian

The relevance of the normalization of petroleum hydrocarbons in soil is due, inter alia, to their ubiquity. Negative impacts on soil cover, atmospheric air, surface and groundwaters, ecological systems and public health are noted at all stages of development of oil fields - from drilling to industrial processing, liquidation of equipment and delivery to the consumer. In addition, various technologies for the destruction of oil contamination (re-cultivation, sanitation, etc.) are actively being developed, but they are not widely used, because there is no norm for a safe level of their content for humans and environmental objects. The article deals with problems of hygienic regulation of petroleum hydrocarbons in the soil. Methods are presented for the quantitative determination of oil and oil products in soil, as well as conceptual issues in the system for estimating oil as a soil pollutant. The subordinate legislation, taking into account the lists of pollutants, in respect of which state regulation measures in the field of environmental protection are applied, are sanctified. Toxic oxygen-containing products are shown to be formed asa result of the transformation of the hydrocarbon component of the component composition of the oil. Threshold concentrations of the safe content of petroleum hydrocarbons in the soil in a vegetation experiment (500 mg/kg), water migration - 10,000 mg/kg and a total of 21,000 mg/kg were determined. Priority directions of research on the establishment of a safe level of oil hydrocarbon contamination in the soil according to the airborne migration index of harmfulness, as well as the quantitative determination of petroleum hydrocarbons in agricultural plants are indicated.


2021 ◽  
Vol 9 (9) ◽  
pp. 1003
Author(s):  
Efsevia Fragkou ◽  
Eleftheria Antoniou ◽  
Ioannis Daliakopoulos ◽  
Thrassyvoulos Manios ◽  
Marianna Theodorakopoulou ◽  
...  

Oil pollution has been a worldwide concern especially in environments where treatment is quite difficult to apply. Marine polluted sediments, in particular, constitute one of the most recalcitrant environments for bioremediation and are often the final repository of petroleum contaminants, as a result of runoff and deposition. Aerobic hydrocarbon degraders present in the sediments are tackling the pollution under oxygen-limited or oxygen-depleted conditions. Research has focused on new ways to enhance bioremediation under anoxic conditions, however aerobic bioremediation is faster, and hence more effort should be made to sustain oxygen concentration levels. In this review, the different bioremediation techniques used for the decontamination of marine sediments are briefly discussed, and focus is primarily given to the different oxygenation methods used for enhancing aerobic bioremediation and the aeration methods that are suitable for in situ application, as well as state of the art technologies that make in situ aeration an appealing approach. Based on the technologies analyzed, suggestions are made for sediment bioremediation techniques in different marine environments.


2019 ◽  
Vol 15 (2) ◽  
pp. 121-129
Author(s):  
Zhi Rao ◽  
Bo-xia Li ◽  
Yong-Wen Jin ◽  
Wen-Kou ◽  
Yan-rong Ma ◽  
...  

Background: Imatinib (IM) is a chemotherapy medication metabolized by CYP3A4 to Ndesmethyl imatinib (NDI), which shows similar pharmacologic activity to the parent drug. Although methods for determination of IM and/or NDI have been developed extensively, only few observations have been addressed to simultaneously determine IM and NDI in biological tissues such as liver, kidney, heart, brain and bone marrow. Methods: A validated LC-MS/MS method was developed for the quantitative determination of imatinib (IM) and N-desmethyl imatinib (NDI) from rat plasma, bone marrow, brain, heart, liver and kidney. The plasma samples were prepared by protein precipitation, and then the separation of the analytes was achieved using an Agilent Zorbax Eclipse Plus C18 column (4.6 × 100 mm, 3.5 µm) with gradient elution running water (A) and methanol (B). Mass spectrometric detection was achieved by a triplequadrupole mass spectrometer equipped with an electrospray source interface in positive ionization mode. Results: This method was used to investigate the pharmacokinetics and the tissue distributions in rats following oral administration of 25 mg/kg of IM. The pharmacokinetic profiles suggested that IM and NDI are disappeared faster in rats than human, and the tissue distribution results showed that IM and NDI had good tissue penetration and distribution, except for the brain. This is the first report about the large penetrations of IM and NDI in rat bone marrow. Conclusion: The method demonstrated good sensitivity, accuracy, precision and recovery in assays of IM and NDI in rats. The described assay was successfully applied for the evaluation of pharmacokinetics and distribution in the brain, heart, liver, kidney and bone marrow of IM and NDI after a single oral administration of IM to rats.


Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 560
Author(s):  
Alexandra Carvalho ◽  
Mariana C. F. Costa ◽  
Valeria S. Marangoni ◽  
Pei Rou Ng ◽  
Thi Le Hang Nguyen ◽  
...  

We show that the degree of oxidation of graphene oxide (GO) can be obtained by using a combination of state-of-the-art ab initio computational modeling and X-ray photoemission spectroscopy (XPS). We show that the shift of the XPS C1s peak relative to pristine graphene, ΔEC1s, can be described with high accuracy by ΔEC1s=A(cO−cl)2+E0, where c0 is the oxygen concentration, A=52.3 eV, cl=0.122, and E0=1.22 eV. Our results demonstrate a precise determination of the oxygen content of GO samples.


2021 ◽  
Vol 22 (12) ◽  
pp. 6283
Author(s):  
Jérémy Lamarche ◽  
Luisa Ronga ◽  
Joanna Szpunar ◽  
Ryszard Lobinski

Selenoprotein P (SELENOP) is an emerging marker of the nutritional status of selenium and of various diseases, however, its chemical characteristics still need to be investigated and methods for its accurate quantitation improved. SELENOP is unique among selenoproteins, as it contains multiple genetically encoded SeCys residues, whereas all the other characterized selenoproteins contain just one. SELENOP occurs in the form of multiple isoforms, truncated species and post-translationally modified variants which are relatively poorly characterized. The accurate quantification of SELENOP is contingent on the availability of specific primary standards and reference methods. Before recombinant SELENOP becomes available to be used as a primary standard, careful investigation of the characteristics of the SELENOP measured by electrospray MS and strict control of the recoveries at the various steps of the analytical procedures are strongly recommended. This review critically discusses the state-of-the-art of analytical approaches to the characterization and quantification of SELENOP. While immunoassays remain the standard for the determination of human and animal health status, because of their speed and simplicity, mass spectrometry techniques offer many attractive and complementary features that are highlighted and critically evaluated.


Materials ◽  
2021 ◽  
Vol 14 (8) ◽  
pp. 1972
Author(s):  
Agnieszka Gierej ◽  
Thomas Geernaert ◽  
Sandra Van Vlierberghe ◽  
Peter Dubruel ◽  
Hugo Thienpont ◽  
...  

The limited penetration depth of visible light in biological tissues has encouraged researchers to develop novel implantable light-guiding devices. Optical fibers and waveguides that are made from biocompatible and biodegradable materials offer a straightforward but effective approach to overcome this issue. In the last decade, various optically transparent biomaterials, as well as different fabrication techniques, have been investigated for this purpose, and in view of obtaining fully fledged optical fibers. This article reviews the state-of-the-art in the development of biocompatible and biodegradable optical fibers. Whilst several reviews that focus on the chemical properties of the biomaterials from which these optical waveguides can be made have been published, a systematic review about the actual optical fibers made from these materials and the different fabrication processes is not available yet. This prompted us to investigate the essential properties of these biomaterials, in view of fabricating optical fibers, and in particular to look into the issues related to fabrication techniques, and also to discuss the challenges in the use and operation of these optical fibers. We close our review with a summary and an outline of the applications that may benefit from these novel optical waveguides.


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