12 research outputs found
Synthesis, characterisation and application iron and manganeous based sorbents for arsenic removal from water
Prisusutvo arsena u podzemnim vodama, koje se primenjuju za vodosnabdevanje stanovništva je globalan problem. Različiti konvencionalni procesi se primenjuju za uklanjanje arsena iz vode, uključujući koagulaciju i flokulaciju, sorpciju, membransku filtraciju i jonsku izmenu. Uzimajući u obzir relativnu nisku cenu, jednostavnu kontrolu procesa i održavanje, visok stepen uklanjanja arsena, sorpcija se smatra jednom od najpodobnijih tehnika za uklanjanje arsena u tretmanu vode za piće. Premda su na tržištu dostupni različiti sorbenti za uklanjanje arsena, postoji potreba za iznalaženjem i razvojem novih low-cost sorbenata, a kojima bi se pak mogao obezbediti visok stepen uklanjanja oba oksidaciona oblika arsena, i As(III) i As(V). Cilj ovog rada bio je usmeren na sintezu i karakterizaciju novih sorbenata na bazi gvožđa i mangana odnosno Fe-Mn binarnog oksida, ispitivanje njihovog potencijala za uklanjanje arsena iz vode i utvrđivanje da li novosintetisani sorbenti po pitanju efikasnosti, mogu konkurisati postojećim komercijalnim i široko korišćenim sorbentima u tretmanima voda. Metodom precipitacije, sintetisani su Fe-Mn binarni oksidi sa različitim Fe:Mn molskim odnosima 1:1, 3:1, 6:1 i 9:1, dok su kombinacijom heterogene nukleacione tehnike i precipitacije, sintetisana i četiri sorbenta magnetnih svojstava (Mag, Mag-Fe, Mag-Mn, Mag-FeMn). Modifikacijom biopolimera Chitosana i GAC, sa Fe-Mn binarnim oksidom, razvijena su preostala dva materijala Chit-FeMn, odnosno GAC-FeMn. Sintetisani sorbenti su karakterisani različitim tehnikama i metodama (SEM/EDS, XRD,FTIR, BET).Fizičko-hemijskom karakterizacijom sintetisanih sorbenata ustanovljeno je da se Fe-Mn binarni oksidi i magnetni materijali, karakterišu relativno velikim specifičnim površinama (109-300 m 2 /g) i zapreminama mezopora (0,144-0,403 cm 3 /g). Velika specifična površina i razvijena mikroporozna struktura uočena je kod GAC-FeMn (996 m 2 /g; 0,394 cm 3 /g). U poređenju sa ostalim sintetisanim sorbentima, Chit-FeMn je karakterisala najmanja specifična površina i zapremina mezopora (1,99 m 2 /g; 0,014 cm 3 /g). XRD analiza Fe-Mn binarnih oksida ukazala je da je fazna struktura sintetisanih Fe-Mn binarnih oksida slična ferihidratu dok je fazna struktura magnetnih materijala ukazala na prisustvo magemita. Ispitivanja kinetike sorpcionog procesa ukazala su da je mehanizam sorpcije As(III) i As(V) na sintetisanim sorbentima sloţena kombinacija površinske hemisorpcije, koja se odvija kroz granični sloj čestica sorbenata i unutarčestične difuzije. Tome u prilog išli su i rezultati FTIR analize kojima je potvrđeno da se sorpcija arsena na sintetisanim sorbentima ostvaruje kroz interakcije hidroksilnih grupa gvožđa prisutnih na površini sorbenata i arsena. Dodatno, pokazano je da se za razliku od sorpcije As(V), sorpcija As(III) na sorbentima koji pored oksida gvožđa sadrže i okside mangana (Fe-Mn binarni oksidi, Mag-FeMn, Mag-Mn,Chit-FeMn i GAC-FeMn) odvija u dva koraka. U prvom koraku As(III) se oksiduje do As(V), dok u drugom koraku, oksidovani As(V) mehanizmom ligandne izmene formira komplekse na površini ovih sorbenata. Afiniteti sorpcije Fe-Mn binarnih oksida (na osnovu Kd vrednosti) za As(III) opadali su u nizu Fe-Mn 3:1 > Fe-Mn 1:1 > Fe-Mn 6:1 > Fe-Mn 9:1 odnosno kod As(V): Fe-Mn 6:1 > Fe-Mn 3:1 > Fe-Mn 9:1 > Fe-Mn 1:1. Kod magnetnih kompozita, najveća Kd vrednost za As(III) i As(V) ustanovljena je kod Mag-FeMn. Uopšteno, Kd vrednosti za As(III), kod magnetnih kompozita, opadale su u nizu: Mag-FeMn > Mag-Mn > Mag > Mag-Fe, Slično, afinitet sorbenata za As(V), opadao je na sledeći način: Mag-FeMn > Mag > Mag-Fe > Mag-Mn. U poređenju sa neimpregniranim, Kd vrednosti bile su daleko veće kod obloţenih materijala, Chit-FeMn i GAC-FeMn, što je ukazalo na značajan doprinos Fe-Mn binarnog oksida adsorpcionom kapacitetu neimpregniranih medija za As(III) i As(V). U odnosu na ostale ispitivane anjone, najveći uticaj na sorpciju oba oblika arsena na svim sintetisanim sorbentima uočen je kod fosfata, dok je uticaj nitrata i hlorida, u svim slučajevima bio bez značaja. Uticaj ispitivanih anjona na sorpciju As(III) i As(V) na Fe-Mn binarnim oksidima, magnetnim materijalima, Chit-FeMn kao i na sorpciju As(V) na GAC-FeMn, opadao je u nizu: fosfati > silikati > karbonati > sulfati > nitrati > hloridi. Slično, uticaj ispitivanih anjona na sorpciju As(III) na GAC-FeMn je opadao na sledeći način: fosfati > silikati > sulfati > karbonati > nitrati > hloridi.Primenom smeše NaCl-NaOH-NaOCl odnosno primenom 0,1 M i 0,5 M rastvora NaOH, ustanovljeno je da se sintetisani sorbenti mogu jednostavno i efikasno regenerisati i višestruko primeniti, što je od izuzetnog značaja sa ekološkog i ekonomskog aspekta. Najmanje smanjenje sorpcionog kapaciteta i za As(III) i za As(V), nakon pet ciklusa sorpcije -desorpcije, ustanovljeno je kod binarnog oksida sa Fe:Mn molskim odnosom 3:1 i Mag-FeMn. Na osnovu rezultata prikazanih u ovom radu, može se zaključiti da sintetisani sorbenti, Fe-Mn binarni oksidi i magnetni kompoziti, posebno Mag-FeMn, mogu biti efikasna i ekonomična alternativa skupim komercijalnim sorbentima i drugim sofisticiranim tehnologijama. Visok oksidacioni i sorpcioni kapacitet ovih materijala, koji obezbeđuje istovremeno uklanjanje oba oksidaciona oblika arsena daje veliku prednost ovim sorbentima i čini ih veoma atraktivnim i obećavajućim u tretmanu voda. Dodatni benefit magnetnih sorbenata, pre svega Mag-FeMn, ogleda se u njegovoj jednostavnoj separaciji iz vodenog medijuma i recirkulaciji u sistemu. Glavne prednosti sintetisanih Chit-FeMn i GAC-FeMn, ogledaju se u mogućnosti njihove primene kao efikasne filtracione ispune.The presence of inorganic arsenic in groundwater used for drinking water supply is a global problem. Different techniques such as oxidation, coagulation, adsorption, ion exchange, and membrane filtration have been developed and applied for arsenic removal from aqueous media. Among these technologies, adsorption is regarded as one of the most promising approaches to remove arsenic from water because of its high efficiency, low cost, simplicity of operation. Although many sorbents for arsenic removal are available on the market, there is still a need to identify and develop new lowcost sorbents which are highly effective in removing both oxidation states of arsenic, As(III) and As(V). This dissertation therefore presents the synthesis and characterization of ten new iron and manganese based sorbents specifically developed for effective As removal. The Fe- Mn binary oxides were prepared with Fe:Mn molar ratios of 1:1, 3:1,6:1 and 9:1, while four heterogeneous magnetic composites (Mag, Mag-Fe,Mag-Mn, Mag-FeMn) were synthesized by combining the heterogeneous nucleation technique with precipitation. The remaining two materials, Chit-FeMn and GAC-FeMn, were created by modifying the Chitosan and GAC biopolymers with Fe-Mn binary oxide (Chit-FeMn and GAC-FeMn).Multiple techniques were applied to determine the physical and chemical characteristics of the resulting sorbents (including SEM/EDS, XRD, FTIR and BET analyses). In order to establish which sorbents show the greatest promise for application during drinking water treatment, the sorption capacity of the sorbents, theAs(III) and As(V) sorption mechanisms, and the impact of various factors relevant to arsenic sorption, including the regeneration potential and the reuse potential of the sorbents, were all investigated in batch experiments. During the physical characterisation, the Fe-Mn binary oxides and magnetic materials were found to have relatively large specific surface areas (109-300 m 2 /g) and mesopore volumes (0.144-0.403 cm 3 /g). A large specific surface area and microporous structure was observed for GAC-FeMn (996 m 2 /g; 0.394 cm 3 /g). In comparison with the other synthesized sorbents, Chit-FeMn has the smallest specific surface area and pore volume (1.99 m 2 /g; 0.014 cm 3 /g). XRD analyses of the Fe-Mn binary oxides indicated that the phase structure of the synthesized Fe-Mn binary oxides was similar to ferrihydrate, while the phase structure of the magnetic materials showed a good agreement with the XRD diffractogram of maghemite. Investigations into As sorption process kinetics have shown that the sorption mechanism for both As(III) and As(V) on the synthesized sorbents is a combination of surface hemisorption, which takes place through the boundary layer of sorbent particles, and intracellular diffusion. The FTIR analyses confirmed that arsenic sorption was accomplished through the interactions of the hydroxyl groups of iron present on the surface of the sorbents and arsenic. In contrast to the sorption of As(V), it was also shown that As(III) sorption onto sorbents containing manganese oxides (Fe-Mn binary oxides, Mag-FeMn, Mag-Mn, Chit-FeMn and GAC -FeMn) takes place in two steps. In the first step As(III) is oxidized to As(V), while in the second step, the oxidized As(V) forms complexes on the surface of the sorbents via ligand exchange. The Fe-Mn binary oxide sorption capacities (expressed as Kd values) for As(III) followed the trend Fe-Mn 3:1 > Fe-Mn 1:1 > Fe-Mn 6:1 > Fe-Mn 9:1, whereas the As(V) trend was Fe-Mn 6:1 > Fe-Mn 3:1 > Fe-Mn 9:1 > Fe-Mn 1:1. In the magnetic composites, the largest Kd value for As(III) and As(V) was obtained for Mag-FeMn. Generally, the Kd values for As(III) in the magnetic composites decreased in the series: Mag-FeMn > Mag-Mn > Mag > Mag-Fe. Similarly, the affinity of the sorbents for As(V) was as follows: Mag-FeMn > Mag > Mag-Fe > Mag- Mn. In comparison to the nonimpregnated materials, the Kd values were much higher for the boated materials, Chit-FeMn and GAC-FeMn, demonstrating the significant advantage Fe-Mn binary oxides provide in increasing As(III) and As(V) adsorption capacities. One of the most problematic limiting factors in applying adsorption technologies during drinking water treatment is the presence of other water constituents which interfere with the adsorption process. Investigations into the inhibitory effect of competive anions on the adsorption of both forms of arsenic revealed that phosphates were the worst offenders in terms ofreducing the arsenic removal efficacy of sorbents investigated. From the largest to the smallest negative influence of the anions investigated, for As(III) and As(V) adsorption on Fe-Mn binary oxides, magnetic materials and Chit-FeMn, as well as As(V) adsorption on GAC-FeMn, the order was: phosphates > silicates > carbonates > sulfates > nitrates > chlorides, with the presence of the latter two anions proving almost irrelevant to the As adsorption process. Similarly, the negative influence of anions on As(III) sorption on GAC-FeMn was: phosphates > silicates > sulphates > carbonates > nitrates > chlorides. Another issue with applying adsorption in real treatment conditions is the need to regularly regenerate and/or replace the spent sorbent. In this work, a simple and efficient process for sorbent rfegeneration is demonstrated. This regeneration process can be applied to the sorbents investigated multiple times, and uses an NaCl-NaOH-NaOCl mixture, or 0.1 M and 0.5 M NaOH solutions. This finding is of great importance from an ecological and economic point of view. The minimum reduction in the sorption capacity for both As(III) and As(V), after five sorption-regeneration cycles, was found in the binary oxide with a 3:1 Fe:Mn molar ratio and Mag-FeMn. Arsenic sorption behaviour was also investigated using real groundwater samples, with the results demonstrating the great potential of 3:1 Fe-Mn binary oxide and Mag- FeMn. However, Chit-FeMn and GAC-FeMn were less effective at adsorbing As from the groundwater samples.Based on the results presented in this dissertation, it can be concluded that the synthesized sorbents, especially the Fe-Mn binary oxides and magnetic composites, and Mag-FeMn in particular, can be efficient and economical alternatives to expensive commercial sorbents and other sophisticated As removal technologies. The high oxidation and sorption capacity of these materials, which ensure the simultaneous removal of arsenic with both oxidation states, is a large advantage for these sorbents and makes them very attractive and promising for application in drinking water treatment. An additional benefit of the magnetic sorbents, primarily Mag-FeMn, is the ease with which they may be separated from the aqueous medium, allowing for simple recirculation within a system. Similarly, the main advantages of the synthesized Chit- FeMn and GAC-FeMn are reflected in their application as effective filtration media
Teratom jajnika u rutinskom bioptičkom materijalu u petogodišnjem razdoblju
Teratomas are tumors derived from germ cells, most frequently arising in the gonads. The aim of this study was to determine the number of ovarian teratomas diagnosed in the routine biopsy material at Ljudevit Jurak Clinical Department of Pathology, Sestre milosrdnice University Hospital Center during a 5-year period, as well as their clinical, gross and microscopic characteristics. Teratomas accounted for 48.6% (n=166) of primary ovarian tumors. The patient mean age
was 34.74±12.37 years. Difference in the incidence of teratoma between the left and right ovary was not significant; bilateral teratoma was found in 13 patients. Teratomas were detected by ultrasonography in 115 (69.27%) cases and the rest were found during surgery performed for other indications. Most teratomas (n=161; 96.9%) were mature and cystic (dermoid cysts). Mature and solid teratomas were diagnosed in 5 (3.01%), ovarian struma in 2 (1.8%) cases and strumal carcinoid in 1 (1.2%) case. Mature cystic teratomas contained sebaceous material in 123 (76.8%) cases, and a total of 16 teeth were found; 157 (94.5%) teratomas measured <10 cm in largest diameter. Microscopically, mature cystic teratomas most frequently contained ectodermal (skin with appendages, mature glia and nerve ganglia) and mesodermal (fibrous, fat tissue, cartilage and bone) tissues. Frequently found tissues of endodermal origin were respiratory and intestinal epithelia. Small foci of thyroid tissue were found in 20 (12%) teratomas. Chronic granulomatous foreign body reaction in the wall of mature cystic teratomas was found in 11 (6.8%) tumors.Teratomi su tumori podrijetla zametnih stanica koji se najčešće razvijaju u gonadama. Cilj rada bio je utvrditi koliko je dijagnoza teratoma jajnika postavljeno na rutinskom bioptičkom materijalu Kliničkoga zavoda za patologiju „Ljudevit Jurak“ Kliničkoga bolničkog centra „Sestre milosrdnice“ u Zagrebu u petogodišnjem razdoblju, kao i koje su bile njihove kliničke, makroskopske i mikroskopske osobine. U analiziranom razdoblju teratomi su sačinjavali 166 (44,86%) primarnih tumora jajnika. Srednja dob bolesnica s teratomom jajnika bila je 35±12,37 godina. Nije pronađena statistički značajna razlika u učestalosti teratoma lijevog i desnog jajnika, a u 13 (7,8%) bolesnica teratom je bio obostran. Teratom je u 115 (69.3%) slučajeva otkriven ultrazvukom, u 21 (12,6%) je ultrazvukom postavljena dijagnoza nespecifi ciranog cističnog tumora, a u 16 (9,6%) slučajeva teratom je otkriven prilikom operacijskog zahvata učinjenog iz nekog drugog razloga. U 160 (96,4%) slučajeva
radilo se o zrelim cističnim teratomima (dermoidnim cistama), od kojih je 123 (76,8%) bilo ispunjeno lojem i u kojima je pronađeno sveukupno 16 zuba. U 157 (94,6%) slučajeva najveći promjer teratoma iznosio je do 10 cm. Mikroskopski, zreli cistični teratomi najčešće su sadržavali tkiva ektodermalnog i mezodermalnog podrijetla i to u 154 (96,3%) slučaja kožu s kožnim adneksima, odnosno u 148 (92,54%) slučaja vezivo. Od drugih ektodermalnih tkiva po učestalosti su slijedili zrela glija i živčani gangliji, a od mezodermalnih tkiva zrelo masno tkivo, hrskavica i kost. Od tkiva endodermalnog podrijetla najčešće je pronađen respiracijski i crijevni epitel. Manja žarišta tkiva štitnjače pronađena su u 19 (12%) cističnih teratoma. U 11 (7%) cističnih teratoma u stijenci su pronađena žarišta kronične upale tipa stranog tijela. Solidne građe bilo je 5 (3%) teratoma, od čega u 3 (2%) slučaja struma jajnika, a u 2 (1%) slučaja strumalni karcinoid
Arsenic Removal from Water by Green Synthesized Magnetic Nanoparticles
Magnetite nanoparticles were synthesized by a simple and ecofriendly method using onion peel (MNp-OP) and corn silk extract (MNp-CS), in order to develop new low-cost adsorbents for arsenic removal from groundwater. As a point of comparison, magnetite nanoparticles were also synthesized with a conventional chemical process (MNp-CO). The antioxidant potential of onion peel and corn silk extracts was determined using ferric reducing antioxidant power (FRAP) and free radical (DPPH) scavenging assays, including the total phenolics, flavonoids and tannins contents. The synthesized magnetite nanoparticles were characterised using different techniques (Scanning electron microscope/Energy dispersive spectroscopy (SEM/EDS), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR) and Brunauer-Emmett-Teller (BET) surface area analyzer). The adsorption capacity of MNp-OP and MNp-CS and the arsenic removal mechanism of these novel adsorbents was investigated through kinetic and equilibrium experiments and their corresponding mathematical models. Characterisation of MNp-OP and MNp-CS shows high BET specific surface areas of 243 m2/g and 261 m2/g, respectively. XRD and FTIR analysis confirmed the formation and presence of magnetite nanoparticles. The arsenic adsorption mechanism on MNp-OP, MNp-CS and MNp-CO involves chemisorption, intraparticle and external diffusion. Maximal adsorption capacities of MNp-OP, MNp-CS and MNp-CO were 1.86, 2.79, and 1.30 mg/g respectively. The green synthesis applied using onion peel and corn silk extracts was cost effective and environmentally friendly, and results in adsorbents with a high capacity for arsenic and magnetic properties, making them a very promising alternative approach in the treatment of arsenic contaminated groundwater
Sorption Behavior of Organic Pollutants on Biodegradable and Nondegradable Microplastics: pH Effects
Microplastics (MPs), chlorinated phenols (CPs), polycyclic aromatic hydrocarbons (PAHs) and halogenated benzenes (HBs) are pollutants that are widely present in freshwater systems. As alternatives to conventional plastics, bioplastics are receiving a lot of attention, but there are limited data on their impact on pollutant behavior. This work therefore investigated the impact of pH on the sorption of CPs, PAHs and HBs, as some of the toxic and highly persistent pollutants, on seven different plastics using kinetic and isotherm studies. The pH of the water matrix impacted the adsorption behavior of CPs on all selected MPs, with the highest degree of adsorption occurring at pH 7 for the majority of the selected CPs. The highest adsorption affinity of CPs on the MPs, at pH 7, was obtained for 4-chlorophenol and 2,4-dichlorophenol on powdered polyethylene standard (qt = 221 μg/g), while the lowest was obtained for the adsorption of pentachlorophenol on polyethylene terephthalate (qt = 25 μg/g). On the other hand, the pH value of the water matrix did not affect the adsorption of halogenated benzenes and PAHs on MPs. The pseudo-second-order rate model fit the adsorption kinetics data of all experiments. The results obtained for the adsorption of CPs on MPs indicated a lower sorption affinity of CPs with MPs at pH 4 and pH 10 compared to pH 7. The Langmuir isotherm, at pH 7, implied that 4-chlorophenol’s adsorption affinity was not significantly influenced by the type of MPs. On the other hand, at pH 7, the adsorption of 2,4-dichlorophenol, 2,4,6-trichlorophenol and pentachlorophenol varied greatly, with powdered MP types showing the highest affinity for CP adsorption. Furthermore, the obtained adsorption isotherm results imply that electrostatic attraction, hydrogen bonds, π-π interactions and van der Waals interactions, are an integral part of adsorption mechanisms of the CPs on the MPs
Impact of Microplastics on the Fate and Behaviour of Arsenic in the Environment and Their Significance for Drinking Water Supply
The ubiquitous presence of microplastics (MPs) is a topic of great concern. Not only do MPs themselves represent potential toxicants for human health, they are never found alone in the environment and interact with and adsorb a variety of toxicologically significant pollutants. This review summarises recent work on interactions between MPs and heavy metals in the environment, with a special focus on arsenic, one of the most widespread and problematic water contaminants. Evidence for the adsorption of arsenic onto MP surfaces is given and the recent research into the consequences of this phenomenon for freshwater, marine, and soil environments presented. Finally, the lack of research into the significance of interactions between arsenic and MPs during drinking water treatment is highlighted. The performance of arsenic removal technologies is governed by a multitude of different factors, and with MPs detected in water sources all over the world, data on how these MPs impact the removal of arsenic and, indeed, other major water contaminants are urgently needed
Photocatalytic Degradation of Magenta Effluent Using Magnetite Doped TiO2 in Solar Parabolic Trough Concentrator
Due to population growth and industrial development consumption of non-renewable energy sources, and consequently pollution, has increased. In order to reduce energy utilisation and preserve the environment, developed and developing countries are increasingly trying to find solutions based on renewable energy sources. Cost-effective wastewater treatment methods using solar energy would significantly ensure effective water source utilisation, thereby contributing towards sustainable development goals. In this paper, special emphasis is given to the use of solar energy as the driving force of the process, as well as the use of highly active magnetic TiO2-based catalysts. Therefore, in this study, we investigated the possibility of photocatalytic degradation of aqueous magenta graphic dye using titanium dioxide as a catalyst and DSD model in order to achieve the best process optimisation. TiO2 was successfully coated with magnetic nanoparticles by one step process and characterized using different techniques (BET, SEM/EDS, FTIR, XRD). Based on DSD statistical method optimal reaction conditions were pH = 6.5; dye concentration 100 mg/L; TiO2–Fe3O4 0.6 g/L, at which the highest degree of magenta dye decolourisation was achieved (85%). Application of solar energy coupled with magnetic TiO2 catalyst which could be recovered and reused makes this approach a promising alternative in green wastewater treatment
Photocatalytic Degradation of Magenta Effluent Using Magnetite Doped TiO<sub>2</sub> in Solar Parabolic Trough Concentrator
Due to population growth and industrial development consumption of non-renewable energy sources, and consequently pollution, has increased. In order to reduce energy utilisation and preserve the environment, developed and developing countries are increasingly trying to find solutions based on renewable energy sources. Cost-effective wastewater treatment methods using solar energy would significantly ensure effective water source utilisation, thereby contributing towards sustainable development goals. In this paper, special emphasis is given to the use of solar energy as the driving force of the process, as well as the use of highly active magnetic TiO2-based catalysts. Therefore, in this study, we investigated the possibility of photocatalytic degradation of aqueous magenta graphic dye using titanium dioxide as a catalyst and DSD model in order to achieve the best process optimisation. TiO2 was successfully coated with magnetic nanoparticles by one step process and characterized using different techniques (BET, SEM/EDS, FTIR, XRD). Based on DSD statistical method optimal reaction conditions were pH = 6.5; dye concentration 100 mg/L; TiO2–Fe3O4 0.6 g/L, at which the highest degree of magenta dye decolourisation was achieved (85%). Application of solar energy coupled with magnetic TiO2 catalyst which could be recovered and reused makes this approach a promising alternative in green wastewater treatment
Changing body structure components and motor skills in military high school students within one year
Background/Aim. Proper growth and development of adolescents in the
morphological, functional and psychosocial aspects is the imperative of the
educational process. The aim of this study was to determine the status and
changes in the indicators of morphological characteristics, motor skills and
lifestyle habits among the students of the Military High School in Belgrade.
Methods. The study included 217 students aged 15 to 18 years (from the first
to the fourth grade). The two measurements performed at the intervals of one
year were used to determine: the body structure by means of 10 variables and
motor skills by 4 variables, while life habits were determined by 25
variables. Results. The differences in the indicators of morphological
characteristics were recorded in all the groups, being the highest in the
first year of schooling. During the period of growing up, a reduction of
fatty component in percentage values was found, as well as an increase of
muscle mass. The progressive growth of motor skills in the first, second and
the third grade was recorded in the manifestation of power, and endurance
improved only in the first year. In terms of dietary habits, there was no
difference among the groups. Conclusion. The obtained results indicate proper
morphological and motor development and the formation of lifestyle habits.
The data obtained will serve as a basis for health and functional prevention
and upgrading in terms of improvement of the process of military education.
[Projekat Ministarstva nauke Republike Srbije, br. III47015
Comparing the Adsorption Performance of Multiwalled Carbon Nanotubes Oxidized by Varying Degrees for Removal of Low Levels of Copper, Nickel and Chromium(VI) from Aqueous Solutions
Functionalized multiwalled carbon nanotubes (MWCNTs) have drawn wide attention in recent years as novel materials for the removal of heavy metals from the aquatic media. This paper investigates the effect that the functionalization (oxidation) process duration time (3 h or 6 h) has on the ability of MWCNTs to treat water contaminated with low levels of Cu(II), Ni(II) and Cr(VI) (initial concentrations 0.5–5 mg L−1) and elucidates the adsorption mechanisms involved. Adsorbent characterization showed that the molar ratio of C and O in these materials was slightly lower for the oxMWCNT6h, due to the higher degree of oxidation, but the specific surface areas and mesopore volumes of these materials were very similar, suggesting that prolonging the functionalization duration had an insignificant effect on the physical characteristics of oxidized multiwalled carbon nanotubes (oxMWCNTs). Increasing the pH of the solutions from pH 2 to pH 8 had a large positive impact on the removal of Cu(II) and Ni(II) by oxMWCNT, but reduced the adsorption of Cr(VI). However, the ionic strength of the solutions had far less pronounced effects. Coupled with the results of fitting the kinetics data to the Elowich and Weber–Morris models, we conclude that adsorption of Cu(II) and Ni(II) is largely driven by electrostatic interactions and surface complexation at the interface of the adsorbate/adsorbent system, whereas the slower adsorption of Cr(VI) on the oxMWCNTs investigated is controlled by an additional chemisorption step where Cr(VI) is reduced to Cr(III). Both oxMWCNT3h and oxMWCNT6h have high adsorption affinities for the heavy metals investigated, with adsorption capacities (expressed by the Freundlich coefficient KF) ranging from 1.24 to 13.2 (mg g−1)/(mg l−1)n, highlighting the great potential such adsorbents have in the removal of heavy metals from aqueous solutions