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Tytuł:
Electrokinetic and flotation behavior of rutile in the presence of lead ions and aluminium ions
Autorzy:
Cheng, Hongwei
Liu, Changmiao
Guo, Zhenxu
Feng, Ansheng
Wei, Min
Lv, Zihu
Wu, Dongyin
Zhao, Dengkui
Powiązania:
https://bibliotekanauki.pl/articles/110558.pdf
Data publikacji:
2019
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
lead ions
aluminium ions
rutile
flotation
Opis:
The effects of Pb(II) ions and Al(III) ions on the electro kinetic and flotation behavior of rutile were investigated by micro-flotation tests, zeta potential measurements and solution chemistry analysis. Micro-flotation results indicate that the Pb(II) ions can effectively improve the flotation recovery of rutile while the Al(III) ions significantly inhibit the flotation of rutile. Zeta potential measurements reveal that a collector styrene phosphoric acid (SPA) can adsorb on the rutile surface after the addition of Pb(II) ions, but hardly adsorb on the rutile surface after the addition of Al(III) ions. Pb(II) ions adsorb on the rutile surface in the form of Pb(OH)+ and Pb(OH)2(s), and the latter one is the main reason that activates rutile flotation. Al(III) ions adsorb on the rutile surface mainly in the form of Al(OH)3(s), which prevent the direct interaction between the rutile and the collector, resulting in a decrease of rutile flotation recovery.
Źródło:
Physicochemical Problems of Mineral Processing; 2019, 55, 2; 458-466
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Application of instruments of nuclear physics to the calculation of theoretical dose distributions in various organs of the human body for beams used in hadrontherapy
Autorzy:
Maliszewska, W.
Sękowski, P.
Skwira-Chalot, I.
Powiązania:
https://bibliotekanauki.pl/articles/146972.pdf
Data publikacji:
2016
Wydawca:
Instytut Chemii i Techniki Jądrowej
Tematy:
carbon ions
hadrontherapy
hydrogen ions
SRIM
Xeloss
Opis:
The area of interests of nuclear physics are studies of reactions, wherein atomic nuclei of projectile collide with target nuclei. An amount of energy lost by projectile nucleus during its passing through the target is a major issue – it is important to know how charged particles interact with matter. It is possible to afford this knowledge by using theoretical programs that calculate energy loss applying the Bethe-Bloch equation. Hadrontherapy, which is a field of still growing interest, is based on the interactions of charged particles with matter. Therefore, there exists a need of creating a simple model that could be used to the calculation of dose distributions in biological matter. Two programs (SRIM, Xeloss), used to the calculation of energy loss by nuclear physicist, have been adapted to determine the dose distributions in analogues of human tissues. Results of the calculations with those programs for beams used in hadrontherapy (e.g. 1H, 12C) will be compared with experimental data available in references.
Źródło:
Nukleonika; 2016, 61, 1; 19-22
0029-5922
1508-5791
Pojawia się w:
Nukleonika
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Influence of diaphragms on measurements of ions emitted from dense magnetized plasmas
Autorzy:
Skladnik-Sadowska, E.
Sadowski, M.
Powiązania:
https://bibliotekanauki.pl/articles/146562.pdf
Data publikacji:
2001
Wydawca:
Instytut Chemii i Techniki Jądrowej
Tematy:
diagnostic of ions
energy distribution
plasma discharges
separate ions
Opis:
The paper concerns the diagnostics of ions escaping from dense magnetized plasma (DMP) discharges. Particular attention is paid to the basic problem of the separation of such ions from the investigated plasma, under the condition that this process should not disturb the velocity (and energy) distribution functions of the measured ions.
Źródło:
Nukleonika; 2001, 46, suppl. 1; 57-60
0029-5922
1508-5791
Pojawia się w:
Nukleonika
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Adsorption kinetic, equilibrium and thermodynamic investigations of Zn(II) and Ni(II) ions removal by poly(azomethinethioamide) resin with pendent chlorobenzylidine ring
Autorzy:
Kumar, P. S.
Ethiraj, H.
Venkat, A.
Deepika, N.
Nivedha, S.
Vidhyadevi, T.
Ravikumar, L.
Sivanesan, S.
Powiązania:
https://bibliotekanauki.pl/articles/780002.pdf
Data publikacji:
2015
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
adsorption
models
Ni(II) ions
poly(azomethinethioamide)
Zn(II) ions
Opis:
This paper reports the application of poly(azomethinethioamide) (PATA) resin having the pendent chlorobenzylidine ring for the removal of heavy metal ions such as Zn(II) and Ni(II) ions from the aqueous solutions by adsorption technology. Kinetic, equilibrium and thermodynamic models for Zn(II) and Ni(II) ions adsorption were applied by considering the effect of contact time, initial metal ion concentration and temperature data, respectively. The adsorption influencing parameters for the maximum removal of metal ions were optimized. Adsorption kinetic results followed the pseudo-second order kinetic model based on the correlation coefficient (R2) values and closed approach of experimental and calculated equilibrium adsorption capacity values. The removal mechanism of metal ions by PATA was explained with the Boyd kinetic model, Weber and Morris intraparticle diffusion model and Shrinking Core Model (SCM). Adsorption equilibrium results followed the Freundlich model based on the R2 values and error functions. The maximum monolayer adsorption capacity of PATA for Zn(II) and Ni(II) ions removal were found to be 105.4 mg/g and 97.3 mg/g, respectively. Thermodynamic study showed the adsorption process was feasible, spontaneous, and exothermic in nature.
Źródło:
Polish Journal of Chemical Technology; 2015, 17, 3; 100-109
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Investigation on different behavior and mechanism of Ca(II) and Fe(III) adsorption on spodumene surface
Autorzy:
Yu, F.
Wang, Y.
Wang, J.
Xie, Z.
Powiązania:
https://bibliotekanauki.pl/articles/110230.pdf
Data publikacji:
2014
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
spodumene surface
calcium ions
iron ions
adsorption mechanism
DFT calculation
Opis:
Behavior and mechanism of Ca2+ and Fe3+ adsorption on spodumene surface were investigated by micro flotation tests, zeta potential measurements, and density functional theory (DFT) calculation methods. The micro flotation tests showed that Ca2+ and Fe3+ activated the flotation of spodumene remarkably. However, the effect of Fe3+ was more significant than that of Ca2+. Additionally, Fe3+ significantly changed the zeta potential of spodumene while Ca2+ showed a little change. Meanwhile, the calculated adsorption energy of Fe3+ on spodumene surface was much greater than that of Ca2+ indicating that Fe3+ is more apt to be adsorbed on spodumene surface than Ca2+. The value of bond population in Ca-O illustrated that the bond of Ca-O consists of partial covalent proportion and some ionic component. On the contrary, the bond of Fe-O showed a relatively strong covalent property. The partial density of states (PDOS) of free Ca/Fe and the reacted O atom on spodumene (110) surface before and after the adsorption showed that Fe 3d orbital and O 2p orbital formed hybridization. The density of states (DOS) near the Fermi level of spodumene surface after adsorption with Fe3+ was much stronger than that with Ca2+.
Źródło:
Physicochemical Problems of Mineral Processing; 2014, 50, 2; 535-550
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Study of process water effect on the activation of sphalerite during differential flotation of Pb-Cu-Zn
Autorzy:
Gutiérrez Pérez, Victor Hugo
Olvera Vázquez, Seydy Lizbeth
Santos Madrid, Rocio
Regino Piña, Rafael
Cruz Ramírez, Alejandro
Rivera Salinas, Jorge Enrique
Alaniz Hernández, Daniel Israel
Powiązania:
https://bibliotekanauki.pl/articles/2146897.pdf
Data publikacji:
2022
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
sphalerite activation
process water
differential flotation
copper ions
lead ions
Opis:
This work was aimed to analyze the effect of concentration of Cu.2+ and Pb.2+ ions in flotation process water with sphalerite activation, the analysis was performed at Cozamin Mining flotation circuit. This analysis demonstrated that (i) it was possible to determine the relationship between Sodium Cyanide and Ammonium Bisulfite used as depressants and Cu.2+ and Pb.2+ contents in the process water. (ii) It also proved the relationship between lead and iron content in the head with the Pb.2+ ions in process water. According to the data gathered and analysis performed, (iii) it was also determined that it was possible to reuse process water as long as the use of Ammonium Bisulfite was reduced and recommended replacing the use of Sodium Cyanide with Zinc Sulfate (ZnSO4) as a depressant of Sphalerite. Additionally, the concentration of Cu.2+ and Pb.2+ ions in the water should be controlled in a range of 10 to 20 ppm and 0.10 to 0.20 ppm, respectively.
Źródło:
Physicochemical Problems of Mineral Processing; 2022, 58, 3; art. no. 146906
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
On the nature of silver ions in complex media
Autorzy:
Loza, K.
Diendorf, J.
Sengstock, C.
Koller, M.
Epple, M.
Powiązania:
https://bibliotekanauki.pl/articles/286036.pdf
Data publikacji:
2014
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
silver ions
biocides
biomaterials
Opis:
Antimicrobial biocides are commonly used to present the growth of bacteria on surfaces and within materials. They are typically added in small quantities to many applications to prevent bacterial growth on the treated object. Silver is increasingly used in many applications due to the aim to replace organic chemical agents by inorganic additives. Examples of applications are bacteriostatic water filters for household use or swimming pool algaecides and numerous devices, ranging from consumer commodities like mobile phones, refrigerators, and clothes to medical devices like catheters, implant surfaces, and plasters. To meet the diversity of application types, many different forms of silver compounds have been developed to serve this market. In particular, there is little information on the types of transformations that silver nanoparticles will undoubtedly undergo in real, complex environments during long-term aging, and the impact of these transformations on their distribution in the environment, bioavailability, and toxicity potential. The biocidal action results from the interaction of silver ions with bacteria. The most potent compounds for a high silver release are soluble silver salts like silver nitrate or silver acetate. These are fully water soluble with a high silver ion release rate. Therefore they are often used as control in cell experiments to elucidate the biological effect of silver nanoparticles. However, in the case of free silver nanoparticles the interactions can be more complex and catalytic reactions on the particle surface which depend on the size and shape of the nanoparticles can render the system very complex. If AgNO3 is used as control, it is tacitly assumed, that the free silver ion concentration is the same as that in the added AgNO3. This obviously cannot be true because of the presence of a whole set of proteins, biomolecules and inorganic ions like Cl- and H2PO4- in the biological medium. These will react with the silver ions in one or the other way. We report on experiments on the behaviour of silver ions in biologically relevant concentrations in different media, from physiological salt solution over phosphate-buffered saline solution to cell culture media. For dissolution and immersion experiments PVP-coated silver nanoparticles were synthesized by reduction with glucose in the presence of PVP. The final silver concentration in all dispersions was determined by atomic absorption spectroscopy. The dissolution of silver nanoparticles was followed in long-term experiments out of a dialysis tube which was permeable only for silver ions. In case of immersion experiments, the nanoparticles and all precipitates were isolated by ultracentrifugation, redispersed in pure water and again subjected to ultracentrifugation. The particles were analyzed by scanning electron microscopy, energy-dispersive X-ray spectroscopy and X-ray powder diffraction. The dissolution requires the presence of dissolved oxygen. If no oxygen is present, only a very small fraction of silver is dissolved, possibly by traces of oxygen in the experimental setup. An oxidizing agent like H2O2 clearly enhances the dissolution. The presence of NaCl, either in pure form or as PBS, strongly slows down the dissolution, probably due to silver chloride formation. Cysteine has a clearly inhibiting effect with almost no dissolution of the silver nanoparticles whereas glucose has a decelerating effect but leads to a similar final dissolved fraction. This suggests that cysteine adsorbs onto the silver nanoparticle surface with its thiol group and prevents the oxidation. In contrast, glucose slows down the dissolution, but clearly did not prevent the oxidation on a longer time scale. We have extended the studies by mixing silver nanoparticle dispersions with different media of increasingly biological nature. The solutions/dispersions were stirred for equilibration and then subjected to ultracentrifugation. All precipitates and nanoparticles were isolated by this way and then analyzed. The results show that both initially present silver ions and released silver ions are mainly precipitated as AgCl if chloride is present. Only in the absence of chloride, glucose is able to reduce Ag+ to Ag0. The initially present silver nanoparticles were recovered in all cases. Silver phosphate was not observed in any case, probably due to the moderate pH (around 7) at which phosphate is mostly protonated to hydrogen phosphate and dihydrogen phosphate. We can conclude that released silver ions precipitate mostly as AgCl in biological media, and that most cell culture studies where silver ions are used as control are in fact studying the effect of colloidal silver chloride on the cells. To prove this assumption, human mesenchymal stem cells (hMSC) were cultured in the presence of silver chloride nanoparticles (diameter 120 nm), and the viability of the cells was analyzed by fluorescence microscopy. In general, we clearly observed that pure silver nanoparticles have lower toxicity to hMSC compared to silver chloride nanoparticles with a comparable total silver dose. Silver acetate in the biological medium had a comparable toxicity to hMSC compared to silver chloride nanoparticles with the same total silver dose.
Źródło:
Engineering of Biomaterials; 2014, 17, no. 128-129; 80
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Biosorption Capacity of Activated Sludge Sand Bed for Removal of Copper from Treated Wastewater
Autorzy:
Trybułowski, Łukasz
Rogowska, Weronika
Zakrzewski, Jakub
Powiązania:
https://bibliotekanauki.pl/articles/2027810.pdf
Data publikacji:
2022
Wydawca:
Polskie Towarzystwo Inżynierii Ekologicznej
Tematy:
copper ions
biosorption
wastewater
Opis:
In this paper, the biosorption capacity of activated sludge sand bed was investigated for copper removal from wastewater. A sand bed consisting of three layers was used for the study: (1) filter gravel with a diameter of 2 to 3 mm, (2) a biological part inoculated with 200 ml of flocculent activated sludge with a dry weight of 5 kg/$m^3$, (3) filter sand with a grain diameter of about 3 mm. The filter was fed with model wastewater prepared with sodium acetate, potassium nitrate, ammonium chloride, and potassium dihydrogen phosphate I and II basic. The source of Cu ions in the wastewater was $CuSO_4$. The model wastewater used in this study was collected every 24 hours. The experiment was terminated when the concentration of Cu in the treated wastewater sample was equal to that in the treated wastewater. Such a phenomenon was indicative of the depletion of the sorption capacity of the tested bed, which was observed after 26 days. The concentration of copper in raw and effluent from the bed was studied using atomic absorption spectroscopy (ASA) in samples mineralized in nitric acid ($HNO_3$) with the addition of perhydrol ($H_2O_2$). Two equilibrium models, Langmuir and Freudlich, were analyzed to study the absorption isotherms.
Źródło:
Journal of Ecological Engineering; 2022, 23, 2; 61-69
2299-8993
Pojawia się w:
Journal of Ecological Engineering
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
A Superconducting Cyclotron as a primary accelerator for exotic beam facilities
Autorzy:
Maggiore, M.
Rifuggiato, D.
Calabretta, L.
Powiązania:
https://bibliotekanauki.pl/articles/146203.pdf
Data publikacji:
2003
Wydawca:
Instytut Chemii i Techniki Jądrowej
Tematy:
cyclotron
ions
medical
superconducting
Opis:
A four sector compact superconducting cyclotron for light ion beams with a maximum energy of 250 MeV/amu has been studied. This cyclotron is mainly designed to accelerate H2 + ions to be extracted by stripping. Ions like C, O or Ne can also be accelerated and extracted by stripping. Extraction by stripping allows to overcome many problems, especially if a certain beam intensity is requested. The preliminary design model of the magnet circuit has been accomplished with the 3D electromagnetic code OPERA [4]. The design of the main coils and of the cryostat has been investigated, too. The features of beam dynamics of this cyclotron, including extraction trajectories, will be presented. Several fields of application have been envisaged for this cyclotron, namely nuclear physics, therapy treatment, interdisciplinary research and radioisotope production using low or medium intensity beams.
Źródło:
Nukleonika; 2003, 48,suppl.2; 165-167
0029-5922
1508-5791
Pojawia się w:
Nukleonika
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Various ionic substitutions in hydroxyapatites - physicochemical studies
Autorzy:
Kolmas, J.
Laskus, A.
Szurkowska, K.
Pajor, K.
Pajchel, Ł.
Powiązania:
https://bibliotekanauki.pl/articles/285828.pdf
Data publikacji:
2018
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
hydroxyapatite
ions
physicochemical analysis
Źródło:
Engineering of Biomaterials; 2018, 21, 148; 45
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Environmentally and Economically Feasibility Manufacturing Process of Potassium Nitrate for Small Scale Industries: A Review
Autorzy:
Joshi, C. S.
Shukla, M. R.
Patel, K.
Joshi, J. S.
Sahu, O.
Powiązania:
https://bibliotekanauki.pl/articles/411997.pdf
Data publikacji:
2015
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
Chemical
discharge
ions
Salts
Waste
Opis:
Potassium Nitrate (PN) is of the basic need of chemical industry. With increase of demand in different production section of fertilizer, pharmaceutical, explosive, food industry etc, potassium nitrate the production becoming non economical to industry. The operating conditions and parameters are the main factors, which responsible for maximised the profits. The main aim of this study is to compared the production potassium nitrate in profitable as well as environmentally suitability way. From the literature different manufacturing process has been summarized for concluding this study.
Źródło:
International Letters of Chemistry, Physics and Astronomy; 2015, 41; 88-99
2299-3843
Pojawia się w:
International Letters of Chemistry, Physics and Astronomy
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Application of polymer inclusion membranes doped with 1-hexyl-4-methylimidazole for pertraction of zinc(II) and other transition metal ions
Autorzy:
Ulewicz, M.
Radzyminska-Lenarcik, E.
Powiązania:
https://bibliotekanauki.pl/articles/110567.pdf
Data publikacji:
2015
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
polymer inclusion membrane
PIM
metal ions separation
zinc(II)
transition metal ions
imidazole derivatives
Opis:
Transport of Zn(II) from unary aqueous chloride solutions and from solutions which contain mixtures of Cd(II), Co(II) and Ni(II) ions in source phases (cMe = 0.001 mol/dm3, pH = 6.0) across polymer inclusion membranes (PIMs) doped with 1-hexyl-4-methylimidazole as ion carrier was studied. The use of 1-hexyl-4-methylimidazole enables the separation of 98.5% Zn(II) from a unary solution and 96.9% from a quaternary solution of Zn(II)-Cd(II)-Co(II)-Ni(II) after running the process for 24 hours. Using that ion carrier, the metals are transported in the following order: Zn(II) > Cd(II) > Ni(II) > Co(II), and the selectivity coefficients of Zn(II)/Cd(II), Zn(II)/Ni(II), and Zn(II)/Co(II) are 12.9, 23.4 and 40.8, respectively. Findings of atomic force microscopy (AFM) examinations as well as thermograms of a polymer inclusion membrane containing 1-hexyl-4-methylimidazole are also presented. A membrane with 1.0 mol/dm3 of carrier has a porosity of 15.8%, and roughness of 6.6 nm. The membranes remain thermally stable at temperatures up to 200oC. The findings were compared with earlier-reported results for 1-hexylimidazole.
Źródło:
Physicochemical Problems of Mineral Processing; 2015, 51, 2; 447-460
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Germanate glasses co-doped with Ce3+/Ln3+ (Ln = Pr, Tb, Dy) for white light emitting diodes
Autorzy:
Górny, Agata
Sołtys, Marta
Pisarska, Joanna
Pisarski, Wojciech A.
Powiązania:
https://bibliotekanauki.pl/articles/173993.pdf
Data publikacji:
2019
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
glasses
rare earth ions
white luminescence
Opis:
Glasses doped with lanthanides ions may be good white light emitters due to their interesting physical and spectroscopic properties. In this paper, the optical spectroscopy of rare earths doped glasses with a special emphasis on application as white LED were presented. The luminescent glass materials containing Ln3+ (Ln = Pr, Tb, Dy) and Ce3+ ions were obtained. The glasses samples were prepared by a traditional melt-quenching technique. The optical properties of glasses containing various concentrations of rare earth ions were analyzed. It was observed that luminescence bands corresponding to characteristic transitions of Ln3+ and cerium ions are present on spectra measured under direct excitation of Ce3+. Therefore, it indicates that the energy transfer process between Ce3+ /Pr3+, Ce3+ /Tb3+, Ce3+ / Dy3+ ions in glasses occurs. Some parameters such as correlated color temperature (CCT) and chromaticity coordinates (CIE) that characterize white LEDs were analyzed and discussed in detail.
Źródło:
Optica Applicata; 2019, 49, 3; 383-391
0078-5466
1899-7015
Pojawia się w:
Optica Applicata
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Analiza struktury chemicznej hydroksyapatytu wzbogaconego jonami Mn 2+ wygrzewanego w wysokiej temperaturze
Structural characterization of thermally processed hydroxyapatite enriched in Mn2+ ions
Autorzy:
Kolmas, J.
Jabłoński, M.
Ślósarczyk, A.
Kołodziejski, W.
Powiązania:
https://bibliotekanauki.pl/articles/286145.pdf
Data publikacji:
2014
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
hydroksyapatyty
biokompatybilność
apatyt
hydroxyapatite
biocompatibility
ions
Opis:
Syntetyczne hydroksyapatyty (HAs), ze względu na wysoką biokompatybilność z ludzkimi tkankami zmineralizowanymi, są szeroko stosowane jako biomateriały w ortopedii oraz stomatologii. Struktura hydroksyapatytu Ca10(PO4)6(OH)2 pozwala na szereg jonowych podstawień, które mogą zachodzić zarówno w pozycji kationów wapnia jak i ortofosforanów oraz strukturalnych grup hydroksylowych. Wprowadzenie dodatkowych jonów do struktury hydroksyapatytu może wpływać na jego właściwości biologiczne i fizykochemiczne. Mangan jest śladowym pierwiastkiem wchodzącym w skład biologicznego apatytu (mineralnego składnika kości oraz zębów). Odgrywa on kluczową rolę w powstawaniu matrycy organicznej. Dodatkowo indukuje integryny, grupę receptorów umożliwiających adhezję komórek. Ostatnio przeprowadzone badania potwierdziły, że hydroksyapatyt wzbogacony jonami manganu Mn2+ wykazuje łatwiejszą osteointegrację niż czysty hydroksyapatyt, dlatego też może być z powodzeniem stosowany jako pokrycie implantów metalicznych. W powyższej pracy wykorzystano standardową metodę mokrą do syntezy hydroksyapatytów zawierających niewielkie ilości jonów Mn2+. Otrzymane próbki wygrzewano następnie w dwóch różnych temperaturach: 800 oraz 1250°C. Głównym celem tej pracy było zbadanie wpływu procesu termicznego na strukturę chemiczną hydroksyapatytuwzbogaconego jonami manganowymi. Do badań fizykochemicznych wykorzystano: proszkową dyfraktometrię rentgenowską (PXRD), mikroskopię elektronową (SEM oraz TEM), spektroskopię w podczerwieni (FT-IR) oraz spektroskopię magnetycznego rezonansu jądrowego w ciele stałym (ssNMR). Wprowadzenie jonów Mn2+ do struktury hydroksyapatytu zostało potwierdzone dzięki zastosowaniu metod PXRD oraz ssNMR. Wykazano także, że obecność manganu ułatwia termiczny rozkład hydroksyapatytu do oksyhydroksyapatytu. Próbki wygrzewane w wyższej temperaturze (1250°) okazały się niehomogeniczne. Zawierały, oprócz fazy hydroksyapatytu, dodatkowe fazy krystaliczne: oksyhydroksyapatyt, oksyapatyt, dziewięciotlenek dwufosforu i czterowapnia (TTCP) oraz α-ortofosforan wapnia (αTCP). Użyte metody fizykochemiczne pozwoliły stwierdzić, że w próbkach kalcynowanych (wygrzewanych w temperaturze 800°C) jony manganowe zajmują przede wszystkim pozycje wapnia Ca(I) w komórce elementarnej hydroksyapatytu. Podczas wygrzewania w wyższej temperaturze dochodzi do częściowego przemieszczenia jonów manganu w pozycje Ca(II).
Synthetic hydroxyapatites (HAs), due to their high compatibility with human mineralized tissues are widely used in implant materials for orthopaedic and dental applications. Hydroxyapatite structure Ca10(PO4)6(OH)2 is tolerant to several ionic substitutions. They can occur in HA for calcium cations, for orthophosphates and structural hydroxyl ions. The incorporation of additional ions into the apatite crystals may change their biological or physicochemical properties. Manganese appears in biological apatite (bone and teeth) and plays a key role in the development of organic matrix. It also induces integrins, receptors mediating cellular interactions with extracellular matrix and cell surface ligands. Manganese-doped HA exhibits better osseointegration than pure HA, thus it may be used as a coating of metallic implants. In this paper, hydroxyapatites enriched in small amounts of manganese ions Mn2+ were synthesized by standard wet method. The obtained samples were heated at two different temperatures: 800 and 1250ºC. The main aim of this study was to determine the influence of thermal processing of hydroxyapatite enriched in Mn2+ ions on its chemical structure. For profound physicochemical studies powder X-ray diffractometry (PXRD), electron microscopy (SEM and TEM), infrared spectroscopy (FT-IR) and solid-state nuclear magnetic resonance (ssNMR) were applied. The incorporation of manganese ions was confirmed using PXRD and ssNMR methods. It was found that the presence of manganese facilitates hydroxyapatite dehydration and decomposition to oxyhydroxyapatite. The samples heated at 1250ºC are not homogenous and contain, apart from hydroxyapatite other crystalline phases: oxyhydroxyapatite, oxyapatite, tetracalcium phosphate (TTCP) and α-tricalcium phosphate (αTCP). In the calcined sample (heated at 800ºC), manganese ions preferentially occupy the Ca(I) position in the hydroxyapatite crystallographic unit cell. During heat treatment at the higher temperature, some Mn2+ ions move to the Ca(II) position.
Źródło:
Engineering of Biomaterials; 2014, 17, no. 128-129; 10-11
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Reduction of chromium(VI) ions from aqueous solutions by using the solvent impregnated resin
Autorzy:
Wójcik, G.
Hubicki, Z.
Powiązania:
https://bibliotekanauki.pl/articles/115625.pdf
Data publikacji:
2011
Wydawca:
Fundacja na Rzecz Młodych Naukowców
Tematy:
sorption of chromium(VI) ions
reduction
Opis:
The solvent impregnated resins enables effective recovery of microquantities of chromium(VI) ions from wastewaters. The solvent impregnated resin (SIR) Amberlite XAD 7 HP as polymer matrix has been prepared by the wet-impregnation technique. Aliquat 336 was employed as the extractant and acetone as the solvents for impregnation. Sorption of chromium(VI) was investigated in the batch process . Sorption of chromium(VI) was studied in the pH range from 1.5 to 7. It was stated that sorption of chromium(VI) ions depends on acidity of solution. The values of recovery factors of chromium(VI) are higher at low pH than in neutral solution. The speciation of chromium was investigated in the studied pH range. Reduction of chromium(VI) to chromium(III) under acidic conditions was observed. Chromium was determined by using the spectrophotometric and atomic absorption spectroscopy methods. Both methods permit to observe changing of valence of chromium(III) and (VI) oxidation states. The prepared SIR is a new sorbent used for recovery of chromium ions from wastewaters.
Źródło:
Challenges of Modern Technology; 2011, 2, 3; 41-43
2082-2863
2353-4419
Pojawia się w:
Challenges of Modern Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Production of negative hydrogen ions using a low-pressure reflex discharge source
Autorzy:
Toader, E.
Powiązania:
https://bibliotekanauki.pl/articles/147442.pdf
Data publikacji:
2006
Wydawca:
Instytut Chemii i Techniki Jądrowej
Tematy:
magnetized plasma
negative ions
plasma sources
Opis:
In this paper we analyze the possibility to use the reflex discharge plasma as a volume source of negative hydrogen ions. The basic internal parameters like the temperature Te and the density ne of the electrons, the density ni of the positive hydrogen ions, the density n- of the negative hydrogen ions, and the negative ion fraction n-/ne are measured and discussed. The operating conditions are optimized within the pressure range 0.1-10 Pa, the discharge power 20-140 watt, and the magnetic field 0-150 gauss. The experiment shows that the enhanced magnetic ionization is the most effective within the pressure range from 0.7 to 4.0 Pa. When p ť 1 Pa the cold electron temperature Te is 0.77 eV, the cold electron density ne is 4.2 ´ 10 18 m-3 and the negative ion density n- is as high as 0.8 x 10 17 m-3. The negative ion fraction n-/ne increases from 1.4% for p = 0.1 Pa to almost 2.2% within the pressure range 1-4 Pa. The positive ion density scales with the power, while the negative ion density and the negative ion fraction seems to saturate at higher power levels.
Źródło:
Nukleonika; 2006, 51, 1; 29-35
0029-5922
1508-5791
Pojawia się w:
Nukleonika
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Supramolecular complexes of cobalt(II), manganese(II) and cadmium(II) with bis(terpyridine) ligand as novel luminescent materials
Autorzy:
Wałęsa-Chorab, M.
Gorczyński, A.
Marcinkowski, D.
Hnatejko, Z.
Patroniak, V.
Powiązania:
https://bibliotekanauki.pl/articles/779935.pdf
Data publikacji:
2013
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
luminescence
supramolecular complexes
transition metal ions
Opis:
Self-assembly of N6-donor bis(terpyridine) ligand L with transition metal ions: Co(II), Mn(II) and Cd(II) leads to a formation of three kinds of supramolecular complexes. In the electronic absorption and emission spectra of supramolecular complexes additional bands were observed what was ascribed to the coordination of ligand molecules to metal ions. Luminescence properties of these complexes strongly depend on the kind of metal ions and counter ions. The effective blue luminescence was observed in the case of Mn(II) and Cd(II) complexes in which all N-donor atoms of ligand molecules coordinate with the metal center.
Źródło:
Polish Journal of Chemical Technology; 2013, 15, 3; 91-95
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Metody usuwania jonów kadmu i ołowiu z roztworów wodnych
Methods of cadmium and lead ions removal from aqueous solutions
Autorzy:
Kasprzyk, P.
Sanak-Rydlewska, S.
Powiązania:
https://bibliotekanauki.pl/articles/394659.pdf
Data publikacji:
2016
Wydawca:
Polska Akademia Nauk. Instytut Gospodarki Surowcami Mineralnymi i Energią PAN
Tematy:
wymiana jonowa
jony kadmu
jony ołowiu
Purolite C160
ion exchange process
cadmium ions
lead ions
Opis:
W pracy zostaną przedstawione metody eliminacji jonów kadmu i ołowiu z roztworów wodnych. Wśród nich wymiana jonowa staje się coraz popularniejszą metodą usuwania zanieczyszczeń ze ścieków przemysłowych. Za tą metodą przemawiają: prostota procesu, niska energochłonność oraz możliwość selektywnego rozdziału zanieczyszczeń. Wymieniacz jonowy używany w procesie można wielokrotnie stosować, bowiem można go poddawać regeneracji. Stosowanie kolumn jonowymiennych umożliwia także budowę modułową linii technologicznej oczyszczania ścieków oraz szybką wymianę modułów według potrzeb technologicznych i składu ścieków. Wymianę jonową można rozpatrywać jako proces membranowy, gdzie membraną jest powierzchnia ziarna – będąca selektywnie przepuszczalną dla wymienianych jonów. W artykule przedstawiono badania laboratoryjne dotyczące wpływu wybranych parametrów procesu na wydajność wymiany jonowej dla jonów kadmu i ołowiu. Pierwiastki te według polskiego prawodawstwa uznane są za substancje szczególnie szkodliwe i mają działanie kancero- i mutagenne. Najwyższa koncentracja tych pierwiastków występuje na terenach uprzemysłowionych oraz na terenach miejskich. Mogą one pochodzić z przemysłu metalurgicznego, produkcji baterii i akumulatorów, ze spalania paliw kopalnych lub produkcji tworzyw sztucznych. Emisja kadmu i ołowiu do środowiska wodnego odbywa się poprzez odprowadzanie wód kopalnianych czy ścieków z przemysłu hydrometalurgicznego lub z galwanizerni. Badania własne wskazują, że eliminacja jonów Pb i Cd najkorzystniej zachodzi w roztworach o pH około 4 i utrzymuje się na wysokim poziomie w zakresie kwaśnego środowiska. Jonit Purolite C-160 umożliwia osiągnięcie współczynnika wydzielania (X) około 99% dla kadmu – tabela 1, natomiast współczynnik ten dla jonów ołowiu nie przekracza 97% – tabela 2.
This article presents the methods of cadmium and lead ions removal from aqueous solutions. The ion exchange method is becoming a more and more popular method of removing impurities from wastewater. The main advantages of this method are: process simplicity, low energy consumption and the possibility of the selective separation of pollutants. The ion exchanger used in the process could be regenerated, therefore, it could be used repeatedly. The use of ion-exchange columns also allows for the modular construction of the process line and the rapid replacement of modules according to the technological needs and composition of the wastewater. Ion exchange can be seen as a membrane process in which the grain surface acts as a membrane – which is selectively permeable to the exchanged ions. The article presents laboratory studies on the influence of the ion exchange process parameters on the efficiency of cadmium and lead ion exchange. These elements are suspected of carcinogenicity and teratogenicity, and according to Polish Legislation, are considered to be harmful substances. The highest concentration of these elements occurs in industrialized areas and in urban areas. They may come from the hydrometallurgical industry, the production of batteries and accumulators from the burning of fossil fuels and the production of plastics. The emission of cadmium and lead into the aquatic environment is done through the discharge the mine water and wastewater from the hydrometallurgical industry and from electroplating. Experiments show that the elimination of Pb and Cd ions preferably occurs in aqueous solutions with a pH around 4. Ion exchange resin Purolite C-160 allows a removal coefficient (X) in the range of about 99% for cadmium to be achieved – Table 5.1, while the same coefficient for lead ions does not exceed 97% – Table 5.2.
Źródło:
Zeszyty Naukowe Instytutu Gospodarki Surowcami Mineralnymi i Energią PAN; 2016, 94; 205-215
2080-0819
Pojawia się w:
Zeszyty Naukowe Instytutu Gospodarki Surowcami Mineralnymi i Energią PAN
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Generation of ·OH initiated by interaction of Fe2+ and Cu+ with dioxygen; comparison with the Fenton chemistry.
Autorzy:
Urbański, Norbert
Beręsewicz, Andrzej
Powiązania:
https://bibliotekanauki.pl/articles/1044216.pdf
Data publikacji:
2000
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
superoxide dismutase
autoxidation
catalase
free radical
Fenton reaction
hydroxyl radical
iron ions
copper ions
desferrioxamine
Opis:
Iron and copper toxicity has been presumed to involve the formation of hydroxyl radical (·OH) from H2O2 in the Fenton reaction. The aim of this study was to verify that Fe2+-O2 and Cu+-O2 chemistry is capable of generating ·OH in the quasi physiological environment of Krebs-Henseleit buffer (KH), and to compare the ability of the Fe2+-O2 system and of the Fenton system (Fe2+ + H2O2) to produce ·OH. The addition of Fe2+ and Cu+ (0-20 μM) to KH resulted in a concentration-dependent increase in ·OH formation, as measured by the salicylate method. While Fe3+ and Cu2+ (0-20 μM) did not result in ·OH formation, these ions mediated significant ·OH production in the presence of a number of reducing agents. The ·OH yield from the reaction mediated by Fe2+ was increased by exogenous Fe3+ and Cu2+ and was prevented by the deoxygenation of the buffer and reduced by superoxide dismutase, catalase, and desferrioxamine. Addition of 1 μM, 5 μM or 10 μM Fe2+ to a range of H2O2 concentrations (the Fenton system) resulted in a H2O2-concentration-dependent rise in ·OH formation. For each Fe2+ concentration tested, the ·OH yield doubled when the ratio [H2O2]:[Fe2+] was raised from zero to one. In conclusion: (i) Fe2+-O2 and Cu+-O2 chemistry is capable of promoting ·OH generation in the environment of oxygenated KH, in the absence of pre-existing superoxide and/or H2O2, and possibly through a mechanism initiated by the metal autoxidation; (ii) The process is enhanced by contaminating Fe3+ and Cu2+; (iii) In the presence of reducing agents also Fe3+ and Cu2+ promote the ·OH formation; (iv) Depending on the actual [H2O2]:[Fe2+] ratio, the efficiency of the Fe2+-O2 chemistry to generate ·OH is greater than or, at best, equal to that of the Fe2+-driven Fenton reaction.
Źródło:
Acta Biochimica Polonica; 2000, 47, 4; 951-962
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Bioaccumulation of uranium from waste water using different strains of Saccharomyces cerevisiae
Autorzy:
Tykva, R.
Novák, J.
Podracká, E.
Popa, K.
Powiązania:
https://bibliotekanauki.pl/articles/148088.pdf
Data publikacji:
2009
Wydawca:
Instytut Chemii i Techniki Jądrowej
Tematy:
bioaccumulation
uranium
Saccharomyces cerevisiae
competitive ions
Opis:
Five different strains of Saccharomyces cerevisiae were tested for their abilities to accumulate uranium from waste water containing competitive ions. Samples of water passing out from a previous uranium mill were used. The strains tested possess different abilities to accumulate uranium. The kinetics of bioaccumulation, the leaching degree, the influence of cell density and their origin were investigated. Under the applied experimental conditions, more than a half of the total activity (uranium and the decay products) could be accumulated after 60 min contact time of 1 mL S. cerevisiae suspension and 5 mL of water. The other cations present in solution effectively competed for the uranium accumulation. 226Ra and its decay products were completely retained using all tested strains.
Źródło:
Nukleonika; 2009, 54, 2; 143-148
0029-5922
1508-5791
Pojawia się w:
Nukleonika
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Electron capture negative ion mass spectra of some freon derivatives
Autorzy:
Asfandiarov, N.
Pshenichnyuk, S.
Fal’ko, V.
Wnorowska, J.
Wnorowski, K.
Szamrej-Foryś, I.
Powiązania:
https://bibliotekanauki.pl/articles/148517.pdf
Data publikacji:
2003
Wydawca:
Instytut Chemii i Techniki Jądrowej
Tematy:
negative ions
electron capture
freon derivatives
Opis:
The temperature dependence of dissociative attachment has been investigated in the temperature range 350-575 K for two freon derivatives 1,1,1-C2H3F2Cl and C2F5Cl using Electron Capture Negative Ion Mass Spectra (ECNI MS). The temperature dependence for 1,1,1-C2H3F2Cl is similar to that observed in the case of CF3Cl reported by Illenberger et al. In contrast, C2F5Cl exhibits quite a different spectrum and its temperature behavior. It has been suggested that sigma*C-Cl delocalization onto two empty orbital leads to Cl- ion formation in two different resonance states.
Źródło:
Nukleonika; 2003, 48, 2; 83-88
0029-5922
1508-5791
Pojawia się w:
Nukleonika
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Determination of the effective diffusivity of cadmium(II) in calcium alginate beads
Autorzy:
Kwiatkowska-Marks, S.
Wójcik, M.
Kopiński, L.
Powiązania:
https://bibliotekanauki.pl/articles/347047.pdf
Data publikacji:
2011
Wydawca:
Politechnika Bydgoska im. Jana i Jędrzeja Śniadeckich. Wydział Technologii i Inżynierii Chemicznej
Tematy:
cadmium ions
alginate beads
effective diffusivity
Opis:
Effective diffusivity (De) of cadmium compounds was calculated in the beads. The study was carried out using two methods: a shrinking core model (SCM) method and a newly developed method named conductometric. It turned out to be a simple and effective method for the calculation of effective diffusivity of Cd(II) in alginate sorbents. The De values obtained by the two methods depended on the alginate content in the beads. However, SCM, in contrast to the conductometric method, gave De values increasing with increasing alginate levels in the beads and lower than the molecular diffusivity of Cd(II), this being inconsistent with the mechanism of diffusion in porous carriers. Hence, the conductometric method can be considered as one giving more reliable results, compared with the SCM method. Moreover, diffusion retardation coefficients for the alginate beads were calculated. Enhanced content of the biopolymer in the beads caused retardation of Cd(II) diffusion in the beads due to the decreasing calculated retardation coefficients with the increasing alginate contents in the beads.
Źródło:
Ars Separatoria Acta; 2011, 8; 11-23
1731-6340
Pojawia się w:
Ars Separatoria Acta
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Effect of divalent metal ions on annexin-mediated aggregation of asolectin liposomes.
Autorzy:
Mel'gunov, Vladimir
Akimova, Elena
Krasavchenko, Kirill
Powiązania:
https://bibliotekanauki.pl/articles/1044309.pdf
Data publikacji:
2000
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
aggregation
liposome
annexin
divalent metal ions
Opis:
Annexins belong to a family of Ca2+- and phospholipid-binding proteins that can mediate the aggregation of granules and vesicles in the presence of Ca2+. We have studied the effects of different divalent metal ions on annexin-mediated aggregation of liposomes using annexins isolated from rabbit liver and large unilamellar vesicles prepared from soybean asolectin II-S. In the course of these studies, we have found that annexin-mediated aggregation of liposomes can be driven by various earth and transition metal ions other than Ca2+. The ability of metal ions to induce annexin-mediated aggregation decreases in the order: Cd2+>Ba2+, Sr2+>Ca2+>>Mn2+>Ni2+>>Co2+. Annexin-mediated aggregation of vesicles is more selective to metal ions than the binding of annexins to membranes. We speculate that not every type of divalent metal ion can induce conformational change sufficient to promote the interaction of annexins either with two opposing membranes or with opposing protein molecules. Relative concentration ratios of metal ions in the intimate environment may be crucial for the functioning of annexins within specialized tissues and after treatment with toxic metal ions.
Źródło:
Acta Biochimica Polonica; 2000, 47, 3; 675-683
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Non-destructive viscometric studies of enzymic milk coagulation III. The effect of pH, temperature and Ca-ions concentration on the secondary phase of milk coagulation
Nie niszczące badania wiskozymetryczne enzymatycznego procesu krzepnięcia mleka III. Wpływ stężenia jonów wapniowych, pH i temperatury na wtórną fazę enzymatycznego krzepnięcia mleka
Autorzy:
Bachman, S.
Klimczak, B.
Gasyna, Z.
Powiązania:
https://bibliotekanauki.pl/articles/1398347.pdf
Data publikacji:
1980
Wydawca:
Instytut Rozrodu Zwierząt i Badań Żywności Polskiej Akademii Nauk w Olsztynie
Tematy:
milk coagulation
immobilized rennin
Ca-ions
Opis:
It was observed that within the pH range between 5.57 and 6.37 the time of development of the secondary phase of the rennet milk coagulation is independent from temperatures between 25° and 35°C. Increased concentration of Ca-ions between 0.66 and 1.1 mg CaCl₂ /ml milk accelerates the formation of the secondary phase.
Kontynuując wcześniej prowadzone prace na temat enzymatycznego procesu krzepnięcia mleka [l, 2] w tej części przedstawiono badania wpływu pH oraz stężenia jonów wapniowych we współdziałaniu z temperaturą na wtórną fazę enzymatycznego krzepnięcia mleka. Do badań zastosowano unieruchomioną renninę. Stwierdzono, że dla wartości pH od 5,57 do 6,37 czas wystąpienia fazy wtórnej jest niezależny od temperatury w zakresie 25-35°C. W miarę zwiększenia wartości pH następował spadek szybkości zmiany lepkości mleka w okresie wtórnej fazy. Wyznaczono zależność stałej szybkości zmian lepkości od stężenia jonów wodorowych: k = k'(H+)0,5. Określono zależność odwrotności czasu wystąpienia fazy wtórnej od stężenia jonów wapniowych w granicach 0,66-1,1 mg CaCl₂ /ml mleka dla temperatur w zakresie 25-35°C. Stwierdzono przyspieszenie wystąpienia fazy wtórnej w miarę wzrostu stężenia jonów wapniowych w mleku.
Źródło:
Acta Alimentaria Polonica; 1980, 06, 3; 135-143
0137-1495
Pojawia się w:
Acta Alimentaria Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The mechanical aspect of titanium ion release after posterior instrumentation for early onset scoliosis
Autorzy:
Danielewicz, Anna
Fatyga, Marek
Wójciak-Kosior, Magdalena
Sawicki, Jan
Różańska-Boczula, Monika
Sowa, Ireneusz
Latalski, Michał
Powiązania:
https://bibliotekanauki.pl/articles/109528.pdf
Data publikacji:
2019
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
scoliosis
metal ions
implant
titanium
mineralization
Opis:
Surgical treatment of early onset scoliosis (EOS) is connected with the risk of early and late complications. The aim of the study is to assess influence of the rod fracture on the titanium ion release (TIR) in traditional growing rods instrumentation for EOS.56 patients treated surgically due to EOS were divided into three groups: 1) a control-patients newly operated due to scoliosis, patients treated with the traditional growing rod (TGR) and TGR who had rod fracture (FGR) and required a surgical revision. Titanium quantification in blood sample, skin fragment (CT –clean tissue) andmacrosco-pically contaminated tissue located near the implant (DT –dirty tissue) was performed using high-resolution emission spectrometry with excitation in inductively coupled plasma.The mean serum titanium level in control, TGR, and FGR groups were 1.93 ± 0.8, 5.61 ± 0.23, and 4.43 ± 0.1 μg/dm3, respectively. The mean CT titanium level in control, TGR, and FGR groups were 0.0045 ± 0.001, 0.0035 ± 0.001and 0.0065 ± 6.8 mg/g, respectively. The mean DT titanium level in TGR and FGR groups was 0.59 ± 0.02, and 1.022 ± 0.03 mg/g, respectively.Implant leadsto the TIR into tissues and blood. Increasing the number of anchors increases the titanium content inthe CT TGR group. Mechanical damage to the implant has no significant effect on the increase of TIR
Źródło:
Physicochemical Problems of Mineral Processing; 2019, 55, 6; 1442-1449
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Wyświetlanie 1-25 z 250

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