Instrumental neutron activation analysis of urinary calculi

Five kinds of urinary stones from 42 patients have been determined for a total of 19 elements by instrumental neutron activation analysis. Of these elements, Ca, Mg, Sr, Na, and Cl are found to be present in the core of all kinds of stones. The differences in elemental composition among the different kinds of stones as well as across the layers of stone are statistically evaluated.     

Simultaneous determination of composition of human urinary calculi by use of artificial neural networks

A new chemometric method, which uses artificial neural networks (ANN), is presented for determination of the composition of urinary calculi. The selected constituents were whewellite, weddellite, and uric acid from which approximately 40% of the urinary calculi obtained from Macedonia patients are composed. The results for the synthetic mixtures were better then those obtained by partial least squares (PLS) regression or by the principal component regression (PCR), because neural networks have better prediction capacity. The generalization abilities of the optimized neural networks were checked using the standard addition method on carefully selected real natural samples.     

Heavy metals as toxicants in big cities

Heavy Metals (HMs) can exert detrimental effects on human health and on the environment. Their ecotoxicological properties are generally well known. As regards human toxicology, new aspects should be taken into consideration—gender and age dependence. The HMs chemical risk can be estimated and in this context, city demography data help to evaluate today's ecological situation (including HMs) and to predict the dynamics of future urbanization.As regards urban atmosphere, motor vehicles (Pb) and industry (V, Ni, Cr, Cd) exert the greatest influence; water, soil, vegetation also experience menace caused by HMs. Urban environments should be protected against contamination posed by HMs: the health status of big cities is dependent on adequate and safe supply of water. Vegetation plays a helpful role in reducing HM content in the atmosphere and the soil. Awareness of the inhabitants regarding the risks posed by HMs also counts as critical factor today. Ecoeducation at the beginning of the new century can be taken into consideration.     

Heavy metals in petroleum-contaminated surface soils in Serbia

Investigation of heavy metal contamination levels as well as their association types with substrates in petroleum-contaminated surface soil was carried out using modified sequential extraction method. In that way, remobilization capacity of metal cations, both in natural conditions and in accidents, has been studied. Moreover, partitioning of heavy metals, originating from spilt oil derivative, among surface soil substrates was estimated. Extreme contamination with lead was discovered, as well as the increased concentrations of zinc and copper. Oil-derived Pb and Zn were found to be distributed between carbonates and amorphous Fe-oxides, whereas Cu was found to be dominantly associated with amorphous Fe-oxides. Appreciable amounts of these metals were also found to be incorporated into more resistant structures. In petroleum-contaminated surface soil, substrates of cadmium are carbonates, whereas nickel has the great affinity toward hydrous Mn-oxides. Cd is proven to be the most mobile metal in oil-contaminated surface soil.     

Heavy metals in river sediments — A chemometrical evaluation

First results are presented to support decisions within projects of recultivation in the Merseburg region. From two places of the river Luppe eight sediment samples were taken at four different days. The total concentrations of Cd, Cr, Cu, Fe, Mn, Ni, Pb, and Zn were determined by ICP-AES after digestion with aqua regia both in the gross samples and in four particle size fractions obtained by wet sieving. Subsequently each fraction was split into six classes by a sequential extraction to characterise the pattern of heavy metal binding form. Questions about the difference of the regions, the importance of the particle size fractions, the mobility of the metals, and the influence of the seasonal factor were tried to answer by the help of chemometrical methods. It was possible to show that the two sampling places situated only about 7 km from each other have different total metal concentrations as well as different binding form patterns. The trend of the heavy metal enrichment in the smallest particle size fraction can easily be seen in two-dimensional diagrams, but could in general not be confirmed statistically for all metals. The consideration of all four factors together (region, particle size fraction, mobilisation class, and time) shows the significant influence caused by all factors and all interactions. Multivariate covariance analysis is used to include also the influence of sampling conditions.Dedicated on the occasion of his 70th birthday to Professor Dr. Klaus Doerffel, who has spent much of his life in teaching and introducing statistical and other chemometrical techniques in Analytical Chemistry     

Heavy metals as indirect causative factors of capillaropathy

By applying systemic analysis to a set of random variables, representing blood or urine concentrations of certain enzymes, lipids and metals, three direct causative factors of capillaropathy, in its early stage, i.e. leucine amino peptidase, free erythrocyte protoporphyrin and C₃-complement, have been found. The interactions between the early stage of capillaropathy and these factors have been quantitatively described and a formula for prognosing the capillaropathy occurrence has been proposed. It has also been shown that the following heavy metals Pb, Cd, Cr, Cu, Mg, Fe and Ca, through their direct or indirect interactions with C₃-complement, exert an influence on the occurrence and intensity of capillaropathy. Since direct causative factors of a given pathology can serve as its markers, the completeness of the set of the capillaropathy markers, formed from the causative factors, and their contributions to this pathology have been evaluated. The results were obtained by examining a population of male residents chronically exposed to heavy metals (Pb, Cu) in the environment.     

Heavy metals as indirect causative factors of capillaropathy

By applying systemic analysis to a set of random variables, representing blood or urine concentrations of certain enzymes, lipids and metals, three direct causative factors of capillaropathy, in its early stage, i.e. leucine amino peptidase, free erythrocyte protoporphyrin and C(3)-complement, have been found. The interactions between the early stage of capillaropathy and these factors have been quantitatively described and a formula for prognosing the capillaropathy occurrence has been proposed. It has also been shown that the following heavy metals Pb, Cd, Cr, Cu, Mg, Fe and Ca, through their direct or indirect interactions with C(3)-complement, exert an influence on the occurrence and intensity of capillaropathy. Since direct causative factors of a given pathology can serve as its markers, the completeness of the set of the capillaropathy markers, formed from the causative factors, and their contributions to this pathology have been evaluated. The results were obtained by examining a population of male residents chronically exposed to heavy metals (Pb, Cu) in the environment.     

Determination of the composition of human urinary calculi composed of whewellite, weddellite and carbonate apatite using artificial neural networks

More than half of the analyzed calculi from patients from Macedonia are composed of whewellite, weddellite and carbonate apatite (as single components or in binary or ternary mixtures). In order to develop a simple and satisfactorily reliable method for quantitative analysis of urinary calculi, the possibility was explored to employ artificial neural networks (ANNs) as a tool for such a purpose. By changing the number of input and hidden neurons, a search was made for the three-layered feed-forward ANN which would give the best performance. The root-mean-square errors (RMSE) for the test samples are: 0.035 for whewellite, 0.064 for weddellite and 0.078 for carbonate apatite. The accuracy of the method was checked using standard-addition method on real samples. The discrepancies between calculated and predicted mass fraction of constituents were in the range acceptable for use of the proposed method in clinical laboratories.     

The use of thermal analysis in determination of some urinary calculi of calcium oxalate

The human urinary calculi are mainly constituted by calcium oxalate, magnesium ammonium phosphate hexahydrate, and uric acid. The ions or molecules are easily characterized by wet chemical methods. The difficulties appear in the differentiation of the hydrates of calcium oxalate (monohydrate COM or Whewellite, and dihydrate COD or Weddelite). A high level of COD in the urinary stones leads, often, inflammation, sharp pain and blood in urine. In the worse cases, they must be extracted by surgical way. The identification of the main components of urinary calculi, the knowledge of the true number of water molecules bounded to the calcium oxalate, and the determination of each hydrate in the mixture, are the interests of this memory. The thermal analysis (simultaneous DTA-TG) was applied on thirty-three urinary calculi. The determination of the calcium oxalate hydrates was confirmed by calorimetry (DSC). This revised version was published online in July 2006 with corrections to the Cover Date.     

Heavy metals and adsorbents effects on activated sludge microorganisms

The sorption of Cu(II) and Cd(II) from synthetic solution by powdered activated carbon (PAC), biomass, rice husk (RH) and activated rice husk (ARH) were investigate under batch conditions. After activated by concentrated nitric acid for 15 hours at 60-65 degrees C, the adsorption capacity for RH was increased. The adsorbents arranged in the increasing order of adsorption capacities to the Langmuir Q degree parameter were biomass > PAC > ARH > RH. The addition of adsorbents in base mix solution had increased the specific oxygen uptake rate (SOUR) activated sludge microorganisms with and without the presence of metals. The increased of SOUR were due to the ability of PAC and RH in reducing the inhibitory effect of metals on microorganisms and provide a reaction site between activated sludge microorganisms and substrates.     

Heavy metals in selected soils of the semi-arid region of Nigeria

Eight soil profiles developed on crystalline basement complex rocks in the semi-arid region of Nigeria were analyzed for total contents of cesium (Cs), chromium (Cr), cobalt (Co), hafnium (Hf), iron (Fe), lanthanum (La), lutetium (Lu), scandium (Sc), thorium (Th), uranium (U) and ytterbium (Yb). The contents range from 50.3–95.4 Cs, 16.1–58.1 Cr, 0.6–9.0 Co, 9.0–34.8 g g^–1 Hf, 0.31–3.69% Fe, 17.2–60.7 La, 60.4–90.6 Lu, 2.6–12.6 Sc, 8.3–21.5 Th, 4.7–9.2 U and 3.6–92 g g^–1, Yb. Their corresponding means were 68.4, 35.1, 4.0, 19.9 g g^–1, 1.70%, 37.1, 79.4, 6.5, 14.7, 6.7 and 5.0 g g^–1. In general, total Cs, Co, Fe, La, U and Yb increased with further increase with depth. On the other hand, Lu, Sc and Th showed no distinct vertical distribution within the profiles. All eleven elements were correlated with the amounts of clay present in the soils, the correlation being stronger for Cs, Th, Yb, Cr and Lu.     

Heavy metals adsorption by novel EDTA-modified chitosan-silica hybrid materials

Ionic liquid based microemulsions were characterized by absorption solvatochromic shifts, (1)H NMR and kinetic measurements in order to investigate the properties of the ionic liquid within the restricted geometry provided by microemulsions and the interactions of the ionic liquid with the interface. Experimental results show a significant difference between the interfaces of normal water and the new ionic liquid microemulsions. Absorption solvatochromic shift experiments and kinetic studies on the aminolysis of 4-nitrophenyl laurate by n-decylamine show that the polarity at the interface of the ionic liquid in oil microemulsions (IL/O) is higher than at the interface of water in oil microemulsions (W/O) despite the fact that the polarity of [bmim][BF(4)(-)] is lower than the polarity of water. (1)H NMR experiments showed that an increase in the ionic liquid content of the microemulsion led to an increase in the interaction between [bmim][BF(4)(-)] and TX-100. The reason for the higher polarity of the microemulsions with the ionic liquid can be explained in terms of the incorporation of higher levels of the ionic liquid at the interface of the microemulsions, as compared to water in the traditional systems.     

Heavy metals and color retention by a synthesized inorganic membrane

In this study, a new type of a double-layer ceramic membrane was used for the filtration of wastewater. The synthesized membrane consists of a macroporous substrate (with pore size of about 0.1 μm) prepared following the colloid filtration technique and a thin film functional layer (with pore size of about 10 nm) carried out according to the sol–gel preparation method.The ceramic membranes were tested for the removal of cadmium, zinc, Methylene Blue and Malachite Green from water under a pressure of 5 bar and a treatment time of 2 h. Liquid filtration and flow tests through these membranes resulted in a rejection rate of 100% for Methylene Blue and Malachite Green. This paper also presents the ability of the tubular membrane prepared to separate heavy metals (cadmium and zinc) from their synthetic aqueous solutions. The influence of the applied pressure, feed solute concentration, feed pH on the rejection of cadmium and zinc ions was studied. Retention rates of cadmium and zinc ions of 100% were observed for an initial feed concentration of 10⁻⁴ mol/L.     

Thermogravimetric analysis of human renal calculi sampled in nineteenth century patients

TG and DTG curves of human renal calculi of patients living in the nineteenth century in the South of Italy are reported and compared with those of presentday patients. Marked differences in calculi composition are found in the two different historical periods, that are hypothetically discussed in terms of different diets and of alimentary customs of countries of the considered patients.Work supported by Consiglio Nazionale delle Ricerche (CNR) of Italy.     

Heavy metals in lake water: a review on occurrence and analytical determination

Many lakes especially in Asia are source of livelihood for the surrounding communities. With increased urbanisation and industrialisation, however, these lakes are threatened with emerging environmental contaminants, including heavy metals. Some heavy metals are harmful to human health and the environment. This review aims to describe the different sampling, sample preparation and pretreatment, and instrumental methods of analysis for heavy metals in lake water. Filtration and acid digestion are common sample treatment methods used prior to analytical determination. Atomic absorption spectroscopy and inductively-coupled plasma – mass spectrometry (ICP-MS) are typical analytical techniques but nowadays ICP-MS is frequently used. This review also describes the sources and extent of heavy metals contamination in different lakes. Although some lakes still have natural levels of heavy metals in the water, many have elevated concentrations due to anthropogenic sources, such as vehicular, household, agricultural, industrial and mining activities.