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Abstract

The issue of mercury emission and the need to take action in this direction was noticed in 2013 via the Minamata Convention. Therefore, more and more often, work and new law regulations are commencing to reduce this chemical compound from the environment. The paper presents the problem of removing mercury from waste gases due to new BREF/BAT restrictions, in which the problem of the need to look for new, more efficient solutions to remove this pollution was also indicated. Attention is paid to the problem of the occurrence of mercury in the exhaust gases in the elemental form and the need to carry out laboratory tests. A prototype installation for the sorption of elemental mercury in a pure gas stream on solid sorbents is presented. The installation was built as part of the LIDER project, financed by the National Center for Research and Development in a project entitled: “The Application of Waste Materials From the Energy Sector to Capture Mercury Gaseous Forms from Flue Gas”. The installation is used for tests in laboratory conditions in which the carrier gas of elemental mercury is argon. The first tests on the zeolite sorbent were made on the described apparatus. The tested material was synthetic zeolite X obtained as a result of a two-stage reaction of synthesis of fly ash type C with sodium hydroxide. Due to an increase, the chemical affinity of the tested material in relation to mercury, the obtained zeolite material was activated with silver ions (Ag+) by an ion exchange using silver nitrate (AgNO3). The first test was specified for a period of time of about 240 minutes. During this time, the breakthrough of the tested zeolite material was not recorded, and therefore it can be concluded that the tested material may be promising in the development of new solutions for capturing mercury in the energy sector. The results presented in this paper may be of interest to the energy sector due to the solution of several environmental aspects. The first of them is mercury sorption tests for the development of new exhaust gases treatment technologies. On the other hand, the second aspect raises the possibility of presenting a new direction for the management and utilization of combustion by-products such as fly ash.

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Authors and Affiliations

Piotr Kunecki
Dorota Czarna-Juszkiewicz
Rafał Panek
Magdalena Wdowin
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Abstract

Obowiązująca dyrektywa IED, a co za tym idzie bardzo rygorystyczne wymagania względem rtęci (Hg) stawiane przez BAT/BREF, zmuszają polską energetykę do poszukiwania nowych wydajnych technologii oczyszczania spalin z gazowych jej form. Obecnie żadne z metod pierwotnych ani wtórych usuwania związków Hg w kraju nie jest w stanie sprostać tym restrykcjom. Wymagań tych nie spełniają nawet powszechnie stosowane metody z wykorzystaniem węgla aktywnego modyfikowanego bromem lub jodem czy też nowoczesne metody stosowane w innych krajach wykorzystujące moduły polimerowe. Związane jest to z dużym zanieczyszczeniem rtęcią paliw kopalnych stosowanych w krajowej energetyce. Dlatego też w ramach projektu pt. „Hybrydowe układy adsorpcyjne do redukcji emisji rtęci z zastosowaniem wysokoefektywnych komponentów polimerowych”, akronim HYBREM, podjęte zostały próby zbudowania innowacyjnej linii technologicznej łączącej kilka technik oczyszczania spalin ze szkodliwych związków rtęci. Do budowy instalacji pilotażowej wykorzystano technologie bazujące na modułach polimerowych oraz iniekcji różnych sorbentów stałych. Zaletą budowanej instalacji będzie jej mobilność, przez co może być testowana na różnych obiektach energetycznych. Otrzymane wyniki oczyszczania spalin przy użyciu zaprojektowanej instalacji pilotażowej pozwolą określić czy zbudowany prototyp jest efektywny w każdych warunkach dla polskich elektrowni opalanych węglem. Wiedza na ten temat pozwoli efektywnie rozwinąć technologie przemysłowe pod kątem oczyszczania spalin z rtęci spełniając jednocześnie wymagania stawiane przez konkluzje BAT/BREF.
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Authors and Affiliations

Magdalena Wdowin
Robert Żmuda
Wojciech Adamczyk
Łukasz Lelek
Sergiusz Mandrela
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Abstract

The use of CaO-based adsorbents has a high potential to capture CO2 from various systems due to its high reactivity with CO2, high capacity, and low cost of naturally derived CaO. The application of CaO-based sorbents to remove carbon dioxide is based on a reversible reaction between CaO and CO2. However, multiple carbonation/calcination cycles lead to a rapid reduction in the sorption capacity of natural CaO, and therefore efforts are made to reduce this disadvantage by doping, regenerating, or producing synthetic CaO with stable sorption properties. In this review, the synthesis methods used to obtain CaO-based sorbents were collected, and the latest research on improving their sorption properties was presented. The most commonly used models to describe the CO2 sorption kinetics on CaO-based sorbents were also introduced. The methods of sorbent regeneration and their effectiveness were summarized. In the last part of this review, the current state of advancement of work on the larger scale, possible problems, and opportunities during scale-up of the calcium looping process were presented. Concluding (i) the presented methods of adsorbent synthesis allow for the production of doped CaO adsorbents on a laboratory scale, characterized by high CO2 capture efficiency and good cyclic stability, (ii) the most commonly used in practice models describing CO2 chemisorption are empirical models and the shrinking core model, (iii) the use of sorbent regeneration allows for a significant improvement in sorption capacity, (iv) the scale-up of both the production of new CaO adsorbents and the CO2 capture technology with their use requires further development.
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Authors and Affiliations

Donata Konopacka-Łyskawa
1
ORCID: ORCID
Natalia Czaplicka
1
Andrzej Szefer
2

  1. Gdansk University of Technology, Faculty of Chemistry, Department of Process Engineering and Chemical Technology, ul. Narutowicza 11/12, 80-233 Gdansk, Poland
  2. FLUOR S.A., ul. Prymasa Stefana Wyszynskiego 11, 44-100 Gliwice, Poland
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Abstract

The paper contains the investigations of physical and chemical parameters of calcareous wastes as residuals in the soda production process. The possibility of using these wastes as a sorbent for dry and wet desulfurization of combustion gases from power stations is the main aim of presented data. The reactivity properties of that sorbent for dry method of desulfurization were obtained by AP test, while for wet method by ABB Flaki. On the basis of the obtained results high level of suitability of calcareous waste for wet dcsulfurization method was established (reactivity SRm* = 0.85), for dry desulfurization method suitability of the sorbent is limited by its high consumption up to 5 kg/kgSO2.
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Authors and Affiliations

Stanisław Słupek
Andrzej Buczek
Andrzej Sadowski
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Abstract

In the 21st century the way to increase the efficiency of new sources of energy is directly related with extended exploration of renewable energy. This modern tendency ensures the fuel economy needs to be realized with nature protection. The increasing of new power sources efficiency (cogeneration, trigeneration systems, fuel cells, photovoltaic systems) can be performed by application of solid sorption heat pumps, regrigerators, heat and cold accumulators, heat transformers, natural gas and hydrogen storage systems and efficient heat exchangers.

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Authors and Affiliations

L. Vasiliev
O. Filatova
A. Tsitovich
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Abstract

The process of sorption of chromium(III) ions with a stationary sorbent layer of bentonite clays was investigated. The main advantages of using bentonites in water purification technologies are described: powerful geological reserves, cheap process of rock extraction, easy preparation for transportation and use, possibility of using waste sorbents in other technol-ogies that is why there is no need in costly regeneration. The influence of various factors (process duration, an adsorbent layer) on the degree of wastewater purification from chromium ions, the effect of pumping speed on the dynamic capacity of the sorbent was studied and the effective volume was determined. The adsorption efficacy increases with the increase of the adsorbent layer, what can be explained by the development of the active sorption surface. As the initial concentration of chromium ions increases, the time of appearance of the first traces of the contaminant at the exit of the column increases, as well as the total time to channeling. The results of the studies indicate a higher adsorption capacity of modified bentonite with respect to Cr3+ ions compared to its natural formula. The cleaning efficacy of the solution with a concentration of chromium ions of 0.5 g∙dm–3 is increased by 5% when using 15 g of modified bentonite and 6,5% in the case one uses 20 g compared to the natural form.
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Authors and Affiliations

Christina Soloviy
1
ORCID: ORCID
Myroslav Malovanyy
1
ORCID: ORCID
Olga Palamarchuk
2
ORCID: ORCID
Iryna Trach
3
ORCID: ORCID
Halyna Petruk
4
ORCID: ORCID
Halyna Sakalova
4
ORCID: ORCID
Tamara Vasylinych
4
ORCID: ORCID
Nataliya Vronska
1
ORCID: ORCID

  1. Lviv Polytechnic National University, Viacheslav Chornovil Institute of Sustainable Development, Department of Ecology and Sustainable Environmental Management, Lviv, Ukraine
  2. Vinnytsia Mykhajlo Kotsiubynskyi State Pedagogical University, Educational and Scientific Institute of Pedagogy, Psychology, Department of Psychology and Social Work, Vinnitsa, Ukraine
  3. Vinnytsia National Technical University, Institute for Environmental Safety and Environmental Monitoring, Department of Ecology and Environmental Safety, Vinnitsa, Ukraine
  4. Vinnytsia Mykhajlo Kotsiubynskyi State Pedagogical University, Faculty of Natural and Geography, Department of Chemistry, Vinnitsa, Ukraine
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Abstract

The article comprises synthesis of magnetically susceptible carbon sorbents based on bio raw materials – beet pulp. The synthesis was performed by one- and two-step methodology using FeCl3 as an activating agent. X-ray diffraction methods showed an increase in the distance between graphene layers to 3.7 Å in biocarbon synthesized by a two-step tech-nique and a slight decrease in inter-graphene distance to 3.55 Å for biocarbon synthesized by an one-step technique. In both magnetically susceptible samples, the Fe3O4 magnetite phase was identified. Biocarbon synthesized by a two-step technique is characterized by a microporous structure in which a significant volume fraction (about 35%) is made by pores of 2.2 and 5 nm radius. In the sample after a one-step synthesis, a significant increase in the fraction of pores with radii from 5 to 30 nm and a decrease in the proportion of pores with radii greater than 30 nm can be detected. Based on the analysis of low-angle X-ray scattering data, it is established that carbon without magnetic activation has the smallest specific area of 212 m2∙сm–3, carbon after one-stage synthesis has a slightly larger area of 280 m2∙сm–3, and after two-stage synthesis has the largest specific surface area in 480 m2∙сm–3. The adsorption isotherms of blue methylene have been studied. Biocarbon ob-tained by two-step synthesis has been shown to have significantly better adsorption properties than other synthesized bio-carbons. Isotherms have been analysed based on the Langmuir model.

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Authors and Affiliations

Christina Soloviy
ORCID: ORCID
Myroslav Malovanyy
ORCID: ORCID
Ihor Bordun
ORCID: ORCID
Fedir Ivashchyshyn
ORCID: ORCID
Anatoliy Borysiuk
Yuriy Kulyk
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Abstract

CaO sorbent dissolved in chloride molten salts was investigated to identify its CO2 capture property. Various molten salt systems with different melting points (CaCl2, LiCl, LiCl-CaCl2, and LiCl-KCl) were used to control the operation temperature from 450 to 850ºC in order to determine the effect of the operation temperature on the chemical reaction between CaO and CO2. The CaO sorbent showed the best performance at 550ºC in the LiCl-CaCl2 molten salt (conversion ratio of 85.25%). This temperature is lower than typical operation temperature of the solid-state CaO sorbent (~700ºC).

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Authors and Affiliations

Sung-Wook Kim
Min Ku Jeon
Kirak Lee
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Abstract

Immunoaffinity chromatography (IAC) is a fundamental isolation and purification tool which is incorporated in a substantial range of therapeutic and diagnostic applications. This study has reappraised the usefulness of immunoaffinity chromatography for the purification of polyclonal antibodies. Protein A based IAC is a convenient and reliable method for purification of IgG, from hyperimmunesera (HIS) raised in experimental animals such as rabbits, guinea pigs and mice to be utilized in pharmaceutics and diagnostics. The 146S fraction of Foot and Mouth Disease virus (FMDV) TCID50=10 5.6 was cultured on a baby hamster kidney cell line 21 (BHK-21), concentrated using salt precipitation method using PEG 6000, purified by size exclusion chromatography (SEC) using Sepharose-30 at 254nm absorbance. Purification of 146S FMDV was analyzed using 12% SDS-PAGE which provided two bands of light and heavy chains. The alum-based vaccine, consisting of ≥10μg of 146S FMDV, was applied in 10 male rabbits and 10 male guinea pigs and two animals of each group were taken as a negative control. The titer of serum was calculated using virus neutralization test. A Protein-A kit (Thermo scientific- 44667, 0528.2) was used to purify HIS raised against 146S FMDV and validated using 12% SDS PAGE in reducing condition. The data demonstrate that protein-A affinity chromatography is an efficient tool for the purification of antibodies from hyper-immune sera raised against 146S FMDV and can be used for the production of diagnostic kits e.g. Enzyme linked immuno-sorbent assay (ELISA) and radioimmunoassay.
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Authors and Affiliations

A. Munir
1
A.A. Anjum
1
I. Altaf
2
A.R. Awan
3

  1. Institute of Microbiology, Faculty of Veterinary Sciences, University of Veterinary and Animal Sciences, Outfall road, Lahore, Pakistan
  2. Quality Operations Laboratory, Faculty of Veterinary Sciences, University of Veterinary and Animal Sciences, Outfall road, Lahore, Pakistan
  3. Department of Biochemistry and Biotechnology, Faculty of Veterinary Sciences, University of Veterinary and Animal Sciences, Outfall road, Lahore, Pakistan

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