Role of the vitamin E model compound Trolox in the prevention of Cr(VI)-induced cellular damage

Given the wide industrial use of chromium (Cr) and its environmental contamination, chromium represents a risk to humans exposed to the metal. Considering that Cr(VI) is a potent oxidizing agent that increases intracellular oxidation and DNA damage, it would be worth considering the pretreatment of cells with antioxidants as a means of preventing Cr(VI)-induced toxicity. The objective of this study was to pretreat yeast cells with the water-soluble vitamin E analogue Trolox in an effort to increase cell tolerance against reactive chromium and reactive oxygen species formed during Cr(VI) reduction. Results revealed a decrease in Cr(VI)-induced cytotoxicity and mitotic gene conversions in Trolox-pretreated cells. The protective effect of Trolox in Cr(VI) induced genotoxicity was confirmed also with the prokaryotic Salmonella typhimurium SOS/umu test. Pretreatment of cells with Trolox (1) increased total Cr bioaccumulation, (2) decreased Cr(VI)-induced intracellular oxidation, (3) decreased Cr(V) persistence and (4) increased OH^? formation in yeast extracts. These findings might be useful in directing future investigations concerning the use of Trolox as a human antioxidant supplement, and in clinical applications related to Cr-induced genotoxicity in occupational and environmental situations where chromium is a problem.     

Removal of selenite using ‘waste’ Fe(III)/Cr(III) hydroxide: Adsorption kinetics and isotherms

Removal of selenite [Se (IV)] from aqueous solution on to industrial solid ‘waste’ Fe(III)/Cr(III) hydroxide as adsorbent was investigated in the present article. Maximum adsorption was found to be at pH 4.0. Pretreated Fe(III)/Cr(III) hydroxide was found to be more efficient for the removal of selenite compared to untreated adsorbent. Langmuir and Freundlich isotherms have been studied. The Langmuir adsorption capacity (Q ₀) of the pretreated and untreated adsorbents was found to be 15.63 and 6.04?mg?g^?1, respectively. The adsorption process fit into the second-order kinetics. Thermodynamic parameters show that the adsorption process is spontaneous and endothermic in the temperature range 32 to 60°C. Coexisting anions vanadate and phosphate significantly affect the adsorption of selenite for both the pretreated and untreated adsorbents. Molybdate, thiocyanate, sulphate, nitrate and chloride do not significantly affect the removal of selenite for pretreated adsorbent.     

Study of sorptive properties of trap systems for selective enrichment of volatile organic compounds from tobacco smoke samples

There is a dearth of data on the consumer product concentrations of iron, lead, and nickel for accurate comparison to be made. The levels of these elements were determined in 85 samples of six different classes of personal care products commonly used in Nigeria using atomic absorption spectrophotometry. The results of the analysis showed that the range of the mean concentrations of Fe was 0.485–1.108 ppm, Pb ND–0.163 ppm, and Ni ND-0.160 ppm. The analytical data have demonstrated that the selected consumer products are possible sources of iron, lead, and nickel exposure. Users can be exposed to these metals directly through dermal contact or inhalation. The regulations relating to cosmetic products give no limit values for heavy metals in cosmetic products, hence, it was difficult to establish if the values obtained in this study are safe or not. Prolonged use of soaps, creams, and detergent containing these elements may pose threat to human health and the environment. This could be responsible for various skin diseases such as allergic skin, follicular and pigmentary disorders, which are common among the users (exposed groups) of these products in Nigeria. A body of evidence has presented a rare example of systemic allergic dermatitis caused by topical application of a mercury-containing cosmetic to the upper lip of a 32-year-old Turkish patient.     

Trichoderma atroviride as a bioremediator of Cu pollution: An in vitro study

Isolated Trichoderma atroviride from Cu-polluted river sediment at the Serdang Industrial Area was studied under in vitro conditions to understand the mechanisms that allowed the fungi to thrive in the Cu-polluted freshwater ecosystem. From this study, adsorption was recognized as the main mechanism of Cu tolerance with 50–85% adsorption during the in vitro experiment. The uptake capacity of the isolate in liquid medium ranged from 0.8 to 11.2 mg g^?1 in the potato dextrose broth medium with increasing Cu concentrations from 25 to 300 mg L^?1. It was found that 2.7–5.0% of Cu was lost due to washing. The high percentage of Cu adsorption and the high uptake capacity of Cu by T. atroviride suggest that it is a potential bioremediator of Cu. However, further studies are needed to confirm its practical use as a bioremediating agent for Cu under field conditions.     

Adsorption and movement of carbaryl in soils: A verification of cosolvent theory and comparison of batch equilibrium and soil thin layer chromatography results

Batch equilibrium and soil thin layer chromatography (TLC) techniques were used to investigate the influence of different volume fractions of organic cosolvents (acetone and methanol) on the adsorption and movement of carbaryl in four different types of Indian soils. L-shaped isotherms were obtained for both the cosolvent–water mixtures at all f _s values and were in close agreement with the Freundlich equation. Higher adsorption was observed on F.R.I. soil (FSL) followed by Alampur soil (ASL), Kalai soil (KL), and Bhoran soil (BSL) at all f _s values for both the cosolvent systems as was anticipated from the K and K _D values. The K and K _D values also confirmed that carbaryl adsorption was higher in methanol–water mixture than acetone–water mixture and decreased with increasing f _s values. The frontal R _f values obtained from soil TLC studies were inversely proportional to the K and K _D values for both the cosolvent systems. The higher K and K _D values and lower R _f values in methanol–water mixtures relative to acetone–water mixtures for all the soils indicated that acetone had a greater potential for ground water contamination compared to methanol. The adsorption data were used to evaluate the cosolvent theory for describing adsorption of carbaryl in acetone–water and methanol–water mixtures. The aqueous phase partition coefficients, K _DW (mol g^?1), normalized with respect to f _oc for carbaryl was evaluated by extrapolating f _s → 0.     

Development and application of cross-linked polyethylenimine for trace metal and metalloid removal from mining and industrial wastewaters

Pollution of water bodies by trace metals is an established problem and several studies have been conducted to deal with it. South Africa is amongst those countries whose water systems are most affected as a result of intensive mining activities. This research was dedicated to the development of an insoluble chelating polymer for use as an adsorbent for abstraction of metal ions from mining and industrial wastewaters. Polyethylenimine (PEI), well known for its metal chelating potential, was cross-linked by epichlorohydrin (ECH) in order to convert it into a water-insoluble form for direct use as an adsorbent. The binding affinity of the cross-linked polyethylenimine (CPEI) to heavy metal ions was assessed as well as its ability to be regenerated for re-use. CPEI exhibited good complexation ability to metal ions with high affinity to Cr and most divalent metal ions. The observed order of complexation was: Cr?>?Zn>?Fe?>?Ni?>?Mn?>?Pb. On the other hand, it showed very poor ability to bind oxo-anions such as SeO₃ ^2? and AsO₂ ^? which has been attributed to the unavailability of suitable functional groups to interact with these ions.     

Effects of β-cyclodextrin on adsorption and desorption of carbofuran in soils of divergent texture

Laboratory studies were conducted to determine the adsorption/desorption equilibrium of carbofuran between four divergently textured soils and distilled water and an aqueous solution of 0.01?mol?L^?1 β-cyclodextrin using a batch equilibrium technique. The determined adsorption isotherms for silt loam soils were of L-shaped, for sandy loam soil S-shaped, in agreement with a Freundlich isotherm. In the presence of β-cyclodextrin, the adsorption of carbofuran to the four soils was lower than with distilled water. Positive hysteresis was observed in all soils with distilled water, negative hysteresis when using a solution of β-cyclodextrin as desorbent. The results indicate the potential use of β-cyclodextrin for remediation of pesticide-contaminated soils.     

Application of Zr(IV) tungstate for removal of metal ions from aqueous solutions

A heteropolyacid Zr(IV) tungstate-based cation exchanger has been synthesized. An amorphous sample, prepared at pH 1.2 and having a Na⁺ ion exchange capacity of 0.92?meq?g^?1, was selected for further studies. Its physicochemical properties were determined using Fourier transform infrared spectrometer, X-ray diffraction, thermogravimetric, and scanning electron studies. To understand the cation exchange behavior of the material, distribution coefficients (K _d) for metal ions in various solvent systems were determined. Some important binary separations of metal ions, namely Mg²⁺–Bi³⁺, Cd²⁺–Bi³⁺, Fe³⁺–Bi³⁺, Th⁴⁺–Bi³⁺, and Fe³⁺–Zn²⁺, were achieved on such columns. The practical utility of these separations was demonstrated by separating Fe³⁺ and Zn²⁺ ions quantitatively in commercial pharmaceutical formulation. The cation exchanger has been successfully applied also for the treatment of industrial wastewater and a synthetic mixture. All the results suggests that Zr(IV) tungstate has excellent potential for the removal of metals from aqueous systems using packed columns of this material.     

Removal of Mo(VI) from aqueous solutions using sulfuric acid-modified cinder: kinetic and thermodynamic studies

Removal of Mo(VI) from aqueous solutions was investigated using cinder modified by sulfuric acid. Various parameters such as pH, agitation time, Mo(VI) concentration, and temperature have been studied. The maximum adsorption of Mo(VI) occurred at pH between 4.0 and 6.0. Kinetic studies showed that the adsorption generally obeyed a pseudo second-order model. The activation energy was 31.4?kJ?mol^?1, indicating that the adsorption process was governed mainly by interactions of physical nature. Furthermore, application of Langmuir and Freundlich isotherm models to the adsorption equilibrium data showed that the adsorption behavior obeyed the Langmuir model. The adsorption capacity was found to be 10.8?g Mo(VI)?kg^?1 adsorbent. Finally, thermodynamic parameters such as ΔH ⁰, ΔS ⁰, and ΔG ⁰ were also evaluated, which showed that the adsorption of Mo(VI) on the treated cinder was endothermic, entropy increasing, and spontaneous. In conclusion, the sulfuric acid-modified cinder was shown to be an inexpensive, effective, and simple adsorbent for the removal of Mo(VI) from water.