Search

Background: Lower urinary tract symptoms (LUTS) are a complex and widespread problem among women, resulting in serious problems in both physical, mental, and social health and occupational activity. Methods: A self-administered survey questionnaire was conducted among 100 women diagnosed with LUTS via Google Forms. Among other things, the level of knowledge and self-assessment of existing knowledge about the condition among affected women and the preventive activities undertaken were assessed. Results: The respondents' level of knowledge varied widely. The average score reached was 66.67% (64.48 ± 24.63%). The study demonstrated that women under 35 years of age (U = 772.5; p = 0.005) and those with higher education (U = 615.5; p < 0.001) had significantly higher levels of knowledge. Conclusions: Women's age and education affect knowledge of incontinence prevention. The common occurrence of lower urinary tract symptoms requires the development of a system of preventive, educational and therapeutic activities. Multilevel cooperation is important to increase the effectiveness of therapy.

In recent years, biochar has emerged as a remarkable biosourced material for addressing global environmental, agricultural, biomedical, and energy challenges. However, the performances of biochar rest in part on finely tuning its surface chemical properties, intended to obtain specific functionalities. In this review, we tackle the surface treatment of biochar with silane and other coupling agents such as diazonium salts, titanates, ionic/non-ionic surfactants, as well as nitrogen-containing (macro)molecules. We summarize the recent progress achieved mostly in the last five years and correlate the nature and extent of functionalization to eye-catchy end applications of the surface-engineered biochar.

A series of new granular carbonaceous adsorbents was prepared via single-stage physical and chemical activation of walnut shells. Their suitability for removing various types of organic pollutants (represented by dyes, surfactants and water-soluble polymers) from the liquid phase was assessed. The activation of the precursor was carried out with CO2 and H3PO4 using conventional heating. Activated biocarbons were characterized in terms of chemical composition, acidic–basic nature of the surface, textural and electrokinetic properties as well as thermal stability. Depending on the type of activating agent used during the activation procedure, the obtained biocarbons differed in terms of specific surface area (from 401 to 1361 m2/g) and the type of porous structure produced (microporosity contribution in the range of 45–75%). Adsorption tests proved that the effectiveness of removing organic pollutants from the liquid phase depended to a large extent on the type of prepared adsorbent as well as the chemical nature and the molecular size of the adsorbate used. The chemically activated sample showed greater removal efficiency in relation to all tested pollutants. Its maximum adsorption capacity for methylene blue, poly(acrylic acid), poly(ethylene glycol) and Triton X-100 reached the levels of 247.1, 680.9, 38.5 and 61.8 mg/g, respectively.

Adsorption processes play a crucial role in air purification, wastewater treatment, soil remediation technologies, noble metals recovery, and long-term energy storage systems [...]

The studies aimed to test the adsorption capacity of two silica-enriched porous materials, synthetic Na-X zeolite and Mn-containing carbon composite, towards Pb(II) and Zn(II) ions in single and mixed systems and in the presence of diclofenac (DCF) and (or) poly(acrylic acid) (PAA). The synthetic zeolite was characterized by a well-developed surface area of 728 m2/g and a pore diameter of 1.73 nm, while the carbon composite exhibited 268 m2/g and 7.37 nm, respectively. Na-X was found to be more efficient than the carbon composite (75–212 mg/g) in adsorbing heavy metal ions in both single and bimetallic systems (322–333 mg/g). In turn, the C/Mn/SiO2 composite was more effective in removing Pb(II) ions from the systems that simultaneously contained DCF or PAA (480 and 476 mg/g, respectively). The Na-X zeolite demonstrated the greatest stability in all the systems studied. The highest stability was observed in the DCF + Pb(II) mixture, in contrast to the carbon composites where the stability was much lower. To evaluate the possibility of regeneration of the solids, HCl proved to be the best desorbent for heavy metal ions (efficiency of 99%). In general, both adsorbents offer promising potential for solving environmental problems.

Activated carbons obtained via the thermochemical treatment of lemon balm and mint herbs were applied for ionic polymers adsorption, which directly affects the stability of these types of aqueous suspensions. The examined carbonaceous materials were characterized by well-developed specific surface area (approximately 1000 m2/g) and mesoporous structure. The adsorbed amounts of anionic poly(acrylic acid) and cationic polyethyleneimine from one-component solutions reached significant levels, but the efficiency of adsorption of these compounds from binary solutions slightly decreased. Moreover, the ionic polymers showed stabilizing properties towards the activated carbons suspensions. For both adsorbents, the most stable suspensions were systems containing both types of polymeric macromolecules with different ionic characters. This was due to the occurrence of electrosteric and depletion stabilization mechanisms. Furthermore, the zeta potential and size of particle aggregates were also influenced by the presence of polymers in the aqueous suspensions of activated carbons.

The adsorption mechanism of different polymers containing ionic polyamino acids monomers in the chain structure at the solid–liquid interface was investigated. Initially, the influence of molecular weight and solution pH on simple polyamino acids (poly(L-aspartic acid) and poly(L-lysine) binding was determined. Considering the obtained dependencies, the polymer adsorption layer conformation was proposed in the systems containing block copolymers (both diblock and symmetrical triblock) consisting of polypeptide as well as poly(ethylene glycol) fragments. The presented studies focused on the application of two experimental methods. The polymer adsorption was carried out using the batch method and the adsorbate concentration was determined spectrophotometrically. Then, the turbidimetric measurements were taken. The analysis of the obtained results showed that the adsorption process of block copolymers depends on two factors. Firstly, the solution pH determines both the nature of the interactions of the copolymer structural units with the solid surface and the conformation of the polypeptide chains. The second parameter influencing the adsorption layer structure is the ratio of the lengths of both blocks. Introducing a short PEG fragment into the polymer main chain may improve the polymer adsorption properties by increasing the number of interactions with the adsorbent surface.

The main objective of this study was to assess the usefulness of the low-quality brown coal, ash obtained as a result of its combustion, as well as used gear oil for the production of mineral-carbon adsorbents. The adsorbents were characterized in terms of textural parameters, acidic-basic character of the surface, mineral matter contribution to the structure, as well as their suitability for drinking water purification. Adsorption tests were carried out against two synthetic dyes—methylene blue and methyl orange. In order to understand the nature of the organic pollutants adsorption, the effect of the initial dye concentration, temperature, and pH of the system as well as the phase contact time were investigated. The obtained mineral-carbon composite and activated carbons significantly differed not only in terms of the elemental composition and chemical character of the surface (from slightly acidic to strongly alkaline), but also showed a very diverse degree of specific surface development (from 21 to 656 m2/g) and the type of porous structure generated (from micro/mesoporous to typically mesoporous). Adsorption tests showed that the efficiency of organic dye removal from aqueous solutions primarily depends on the type of the adsorbent and adsorbate applied, and, to a lesser extent, on the temperature and pH of the system. In turn, kinetic studies have shown that the sorption of dyes on such materials is consistent with a pseudo-second-order kinetics model, regardless of the type of adsorbed dye.

The main purpose of the investigations was to explore the protein adsorption on porous materials, as well as to identify the mechanisms of protein attachment without and with other common environmental contaminants, such as drugs, polymers or surfactants. This study applied the Na-X zeolite for the adsorption of bovine serum albumin (BSA) from solutions with various pH values. Electrophoretic mobility measurements and potentiometric titrations were conducted in systems containing both protein and/or PAA (poly(acrylic acid) polymer/DCF (diclofenac) drug/SDS (sodium dodecyl sulfate) surfactant to investigate the protein binding mechanisms in the complex adsorbate systems. In addition, aggregate size and stability measurements were performed in the investigated systems. Based on the research results, it was possible to conclude that the protein adsorbed most preferably on the zeolite surface at a pH value close to its isoelectric point (pI) (102.15 mg/g), and protein adsorption was the lowest in the solutions with strongly alkaline (29.61 mg/g) or acidic (77.45 mg/g) pH values. Thus, the examined zeolitic material can be considered an effective adsorbent for protein removal from an aqueous solution.

Water resources are increasingly degraded due to the discharge of waste generated in municipal, industrial and agricultural areas. Therefore, the search for new materials enabling the effective treatment of drinking water and sewage is currently of great interest. This paper deals with the adsorption of organic and inorganic pollutants on the surface of carbonaceous adsorbents prepared by thermochemical conversion of common pistachio nut shells. The influence of the direct physical activation with CO2 and chemical activation with H3PO4 on parameters, such as elemental composition, textural parameters, acidic–basic character of the surface as well as electrokinetic properties of the prepared carbonaceous materials was checked. The suitability of the activated biocarbons prepared as the adsorbents of iodine, methylene blue and poly(acrylic acid) from the aqueous solutions was estimated. The sample obtained via chemical activation of the precursor turned out to be much more effective in terms of all the tested pollutants adsorption. Its maximum sorption capacity toward iodine was 1059 mg/g, whereas in relation to methylene blue and poly(acrylic acid) 183.1 mg/g and 207.9 mg/g was achieved, respectively. For both carbonaceous materials, a better fit to the experimental data was achieved with a Langmuir isotherm than a Freundlich one. It has also been shown that the efficiency of organic dye, and especially anionic polymer adsorption from aqueous solutions, is significantly affected by solution pH and temperature of the adsorbate–adsorbent system.

[recenzja książki Dzieci w Anus Mundi. Największa hańba ludzkości. Nazistowskie obozy zagłady]

This paper deals with the adsorption of organic and inorganic pollutants on the surface of carbonaceous adsorbents prepared via the chemical activation of expired or broken food products—the solid residue of the “cola-type” drink as well as spoilt grains of white rice and buckwheat groats. The activation process was conducted in the microwave furnace with the use of two activating agents of different chemical nature—potassium carbonate and orthophosphoric acid. The activated carbons were characterized based on the results of elemental analysis, low-temperature nitrogen adsorption/desorption, Boehm titration, thermal analysis, and scanning electron microscopy. Additionally, the suitability of the materials prepared as the adsorbents of methylene blue and iodine from the aqueous solutions was estimated. The materials obtained via chemical activation with H3PO4 turned out to be much more effective in terms of both model pollutant adsorptions. The maximum sorption capacity toward iodine (1180 mg/g) was found for the white-rice-based activated carbon, whereas the most effective in the methylene blue removal (221.3 mg/g) was the sample obtained from the solid residue of the expired “cola-type” drink. For all carbonaceous materials, a better fit for the experimental adsorption data was obtained with the Langmuir isotherm model than the Freundlich one.

The main aim of this study was the determination of temperature influence on adsorption mechanisms of anionic poly(acrylic acid) (PAA) and cationic polyethylenimine (PEI) on the surface of activated carbons (AC) obtained via chemical activation of nettle (NE) and sage (SA) herbs. All measurements were performed at pH 3 at three temperature values, i.e., 15, 25 and 35 °C. The adsorption/desorption of these polymers from single and mixed solution of adsorbates was also investigated. The viscosity studies were additionally performed to obtain hydrodynamic radius values characterizing polymeric macromolecules conformation in the solution. These data are very important for the explanation of changes of linear dimensions of polymer chains with the rise of temperature caused by the modification of polymer–solvent interactions. Moreover, the XPS studies for the systems showing the highest adsorbed amounts in the specific temperature conditions were carried out. These were the systems containing PEI, PAA and NE–AC activated carbon at 25 °C. In such a case, the maximum adsorption capacity towards PAA macromolecules from a single solution of adsorbate reaches the value of 198.12 mg/g. Additionally, the thermodynamic parameters including the free energies of adsorption, as well as changes in free enthalpy and entropy were calculated.

The main objective of this study was to prepare a series of biochars and activated biocarbons via conventional pyrolysis as well as chemical or physical activation of solid residue after solvent extraction of wild growing plant (popular weed)–mugwort. The influence of the variant of the thermochemical treatment of the precursor on such parameters as elemental composition, textural parameters, acidic-basic character of the surface as well as adsorption abilities of the prepared carbonaceous materials was checked. Moreover, the suitability of the biochars prepared as renewable fuels was also investigated. It has been shown that the products obtained from the mugwort stems differ in many respects from the analogous materials obtained from mugwort leaves. The products were micro/mesoporous materials with surface area reaching 974.4 m2/g and total pore volume–1.190 cm3/g. Surface characterization showed that chemical activation with H3PO4 results in the acidic character of the adsorbents surface, whereas products of pyrolysis and especially physical activation show strongly alkaline surface properties. All the adsorbents were used for methylene blue and iodine adsorption from the aquatic environment. To understand the nature of the sorption process, the Langmuir, Freundlich and Temkin isotherm models were employed. The Langmuir model best described the experimental results, and the maximum sorption capacity calculated for this model reached 164.14 mg of methylene blue per gram of adsorbent. In case of iodine removal, the maximum capacity reached 948.00 mg/g. The research carried out for the biochars prepared via conventional pyrolysis showed that the value of their heat of combustion varies in the range from 21.74 to 30.27 MJ/kg, so they can be applied as the renewable fuels.

Nettle and the sage herbs were used to obtain carbonaceous adsorbents. For the biochar preparation the precursors were dried and subjected to conventional pyrolysis. Activated carbons were obtained during precursor impregnation with phosphoric(V) acid and multistep pyrolysis. The textural parameters and acidic-basic properties of the obtained adsorbents were studied. The activated carbons prepared from the above herbs were characterized by the largely developed specific surface area. The obtained carbonaceous adsorbents were used for polymer removal from aqueous solution. Poly(acrylic acid) (PAA) and polyethylenimine (PEI) were chosen, due to their frequent presence in wastewater resulting from their extensive usage in many industrial fields. The influence of polymers on the electrokinetic properties of activated carbon were considered. PAA adsorption caused a decrease in the zeta potential and the surface charge density, whereas PEI increased these values. The activated carbons and biochars were used as polymer adsorbents from their single and binary solutions. Both polymers showed the greatest adsorption at pH 3. Poly (acrylic acid) had no significant effect on the polyethylenimine adsorbed amount, whereas PEI presence decreased the amount of PAA adsorption. Both polymers could be successfully desorbed from the activated carbons and biochar surfaces. The presented studies are innovatory and greatly required for the development of new environment protection procedures.

This paper deals with the adsorption of heavy metal ions on the surface of carbonaceous materials obtained via the chemical activation of biomass. Waste plum stones, pine sawdust and horsetail herb were used as the precursors of carbonaceous adsorbents. The effect of the precursor type and preparation procedure on the physicochemical properties of activated biocarbons and their sorption abilities towards Pb(II) and Cu(II) ions have been checked. The obtained micro-mesoporous activated biocarbons were characterized by determination of elemental composition and ash content, the number of surface functional groups and pH of water extracts as well as textural study based on low temperature nitrogen adsorption/desorption and scanning electron microscopy. Additionally, the electrokinetic studies including solid surface charge density and zeta potential determination were performed. Moreover, the adsorption data modelling (equilibrium and kinetics), XPS results analysis and comparison of parameters characterizing electrical double layer formed at the solid-liquid interface enabled the specification of the mechanism of heavy metals binding with the activated biocarbons surface. The maximum adsorption capacity towards copper and lead ions (177.5 and 178.1 mg/g, respectively) was found for plum stone-based activated biocarbon. For all carbonaceous materials, better fit to the experimental data was achieved with a Langmuir isotherm than a Freundlich one. In turn, a better fit of the kinetics data was obtained using the pseudo-second order model.

The worldwide production of colored products and intermediates is increasing year on year. The consequence of this is an increase in the number of liquid effluents containing toxic dyes entering the aquatic environment. Therefore, it is extremely important to dispose of them. One of the techniques for the elimination of environmentally harmful dyes is adsorption. The main purpose of this study was to explore the possibility of using a carbon and silica (C/SiO2)-based composite for the removal of the azo dye C.I. Basic Red 46 (BR46). The adsorption capacity of C/SiO2 was found to be temperature dependent and increased from 41.90 mg/g to 176.10 mg/g with a temperature rise from 293 K to 333 K in accordance with the endothermic process. The Langmuir isotherm model seems to be the better one for the description of experimental data rather than Freundlich or Dubinin–Radushkevich. The free energy (ΔGo) confirmed the spontaneous nature of BR46 adsorption by C/SiO2. Kinetic parameters revealed that BR46 uptake followed the pseudo-second-order equation; however, the external diffusion plays a significant role. Surfactants of cationic, anionic and non-ionic type influenced BR46 retention by C/SiO2. The electrokinetic results (solid surface charge density and zeta potential) indicated that the adsorption of cationic dye and surfactant influences the structure of the electrical double layer formed at the solid–liquid interface.

Considering the growing needs of environmental remediation, new effective solutions should be sought. Therefore, the adsorbed amounts of heavy metal ions, such as lead(II) and zinc(II), on the surface of high-carbon fly ash (HiC FA), zeolite-–carbon composite (Na-P1(C)) and pure zeolite (Na-P1), were investigated. The applied solids were characterized using the following techniques: XRD, SEM-EDS, TEM, porosimetry, SLS, electrophoresis and potentiometric titration. The heavy metal concentration in the probes was determined by applying ICP-OES spectroscopy. Adsorption/desorption and electrokinetic measurements were performed in the systems containing one or two adsorbates. The obtained results indicated that Pb(II) ions are adsorbed in larger amounts on the investigated solid surface due to the molecular sieving effect. The largest adsorption capacity relative to lead(II) ions was observed for pure Na-P1 zeolite (407 mg/g). The simultaneous presence of Pb(II) + Zn(II) mixed adsorbates minimally affects the amount of adsorbed Pb(II) ions and causes a significant decrease of Zn(II) ion adsorption (in comparison with analogous systems containing single adsorbates). It was also shown that all solids can be efficiently regenerated using hydrochloric acid. Thus, the selected pure zeolite can be successfully applied in soil remediation or other purifying technologies as an effective Pb(II) adsorbent.

Treatment of wastewaters containing hazardous substances such as dyes from the textile, paper, plastic and food industries is of great importance. Efficient technique for the removal of highly toxic organic dyes is adsorption. In this paper, adsorptive properties of the carbon-silica composite (C/SiO2) were evaluated for the cationic dyes C.I. Basic Blue 3 (BB3) and C.I. Basic Yellow 2 (BY2). The sorption capacities were determined as a function of temperature (924.6–1295.9 mg/g for BB3 and 716.3-733.2 mg/g for BY2 at 20–60 °C) using the batch method, and the Langmuir, Freundlich and Temkin isotherm models were applied for the equilibrium data evaluation using linear and non-linear regression. The rate of dye adsorption from the 100 mg/L solution was very fast, after 5 min. of phase contact time 98% of BB3 and 86% of BY2 was removed by C/SiO2. Presence of the anionic (SDS), cationic (CTAB) and non-ionic (Triton X-100) surfactants in the amount of 0.25 g/L caused decrease in BB3 and BY2 uptake. The electrokinetic studies, including determination of the solid surface charge density and zeta potential of the composite suspensions in single and mixed adsorbate systems, were also performed. It was shown that presence of adsorption layers changes the structure of the electrical double layer formed on the solid surface, based on the evidence of changes in ionic composition of both surface layer and the slipping plane area. The greatest differences between suspension with and without adsorbates was obtained in the mixed dye + SDS systems; the main reason for this is the formation of dye-surfactant complexes in the solution and their adsorption at the interface.

Pure zeolite (Na-X) and a zeolite–carbon composite (Na-X(C)) were investigated as adsorbents of heavy metals—Pb2+ and Zn2+ from an aqueous solution. These materials were synthesized from fly ash—a waste from conventional hard coal combustion. Both solids were characterized using XRD, SEM-EDS, nitrogen adsorption/desorption, particle size and elemental composition analyses. The adsorption study was performed at pH 5 in the systems containing one or two adsorbates simultaneously. The obtained results showed that the pure zeolite was characterized by a more developed surface area (728 m2/g) than its carbon composite (272 m2/g), and the mean pore diameters were equal to 1.73 and 2.56 nm, respectively. The pure Na-X zeolite showed better adsorption properties towards heavy metals than its Na-X(C) composite, and Zn2+ adsorbed amounts were significantly higher than the Pb2+ ones (the highest experimental adsorption levels were: for Zn2+—656 and 600 mg/g, and for Pb2+—575 and 314 mg/g, on the Na-X and Na-X(C) surfaces, respectively). The zinc ions are exchanged with the cations inside the zeolite materials structure more effectively than lead ions with a considerably larger size. In the mixed systems, the competition between both heavy metals for access to the active sites on the adsorbent surface leads to the noticeable reduction in their adsorbed amounts. Moreover, the hydrochloric acid was a better desorbing agent for both heavy metals, especially Pb2+ one (desorption reached 78%), than sodium base (maximal desorption 25%).

The adsorption and electrokinetic properties, as well as the stability of the mixed oxide suspensions in the absence and presence of poly(vinyl alcohol) – PVA were studied. Two alumina-silica-titania (AST) oxides were used: AST50 (TiO2 : 50 %, SiO2 : 28 %, Al2O3 : 22 %) and AST71 (TiO2 : 71 %, SiO2 : 8 %, Al2O3 : 21 %). All measurements were carried out in the pH range 3 – 9 as a function of the polymer molecular weight (72 000 and 100 000 Da) and degree of PVA hydrolysis (86 % and 98 %). The obtained results indicated that the PVA adsorption strongly depends on the solution pH – for AST50 it decreases and for AST71 increases with the pH rise. This is caused by various PVA chains conformation on the solid surfaces with different structures. The adsorption of poly(vinyl alcohol) influences on the stability of the mixed oxides suspension. The greatest effects were observed in the presence of PVA 100 000 at pH 3 for AST50 suspension and at pH 9 for AST71 system. In these cases, polymer addition leads to significant improvement of stability conditions of examined systems.DOI: http://dx.doi.org/10.5755/j01.ms.22.2.7778

In this paper adsorptive removal of hazardous dye C.I. Reactive Black 5 from aqueous solutions was investigated using the mixed silica–alumina oxides including of 4% SiO 2 and 96% Al 2 O 3 as well as 97% SiO 2 and 3% Al 2 O 3 . The kinetic studies revealed that with the increasing initial dye concentration from 10 to 30 mg/l and contact time from 1 to 240 min, the sorption capacities ( q t ) increased and the equilibrium was observed after 240 min. Sorption of C.I. Reactive Black 5 on 4% SiO 2 and 96% Al 2 O 3 and 97% SiO 2 and 3% Al 2 O 3 takes place through the pseudo-second-order mechanism rather than the pseudo-first-order one. The experimental data were fitted using the Langmuir and Freundlich isotherm models. The effect of the auxiliaries such as anionic surfactant (sodium dodecyl sulphate) and sodium chloride on C.I. Reactive Black 5 removal was investigated in the 10 mg/l C.I. Reactive Black 5–0.1–1 g/l sodium dodecyl sulphate or 5–20 g/l NaCl systems. The potentiometric titrations indicated that the presence of C.I. Reactive Black 5 changed the surface charge density of silica–alumina mixed oxides, especially in the case of 4% SiO 2 and 96% Al 2 O 3 system.

The influence of metal oxide type on the adsorption affinity of anionic polyacrylamide for the solid surface was studied. There were selected three metal oxides: chromium(III) oxide, zirconium(IV) oxide and aluminium(III) oxide. The adsorption behaviour of high-molecular weight polymer containing 30% of carboxyl groups was determined based on the results of spectrophotometric, electrokinetic and turbidimetric measurements. The anionic polymer exhibits the greatest adsorption on the surface of chromium(III) oxide whereas PAM affinity for the aluminium(III) oxide is the lowest. The polymer presence has a pronounced impact on the electrokinetic properties of examined suspensions manifesting in changes in pH pzc and pH iep values of PAM-containing systems compared to those without polyacrylamide. The anionic PAM addition at pH 6 has the greatest effect on the stability of metal oxide aqueous suspensions.

In this study, a comparison of the properties of homocysteine and homocystine adsorption at mercury/chlorate(VII) interface was done. The adsorption of homocysteine and homocystine is in fact the adsorption of mercury(II) cysteine thiolate and mercury(I) cysteine thiolate. The differences in the capacity curves result probably from the formation of mercurous thiolate at the mercury surface. It seems that the changes in E z and γ z values accompanying the change in the amino acid protonation in the basic electrolyte solution, confirm the altered arrangement of the cysteine mercury thiolates on the electrode surface.

Intracellular Toll-like receptor 3 (TLR3) recognizes viral double-stranded RNA (dsRNA) and activates antiviral immune responses through the production of type I interferons (IFNs) and inflammatory cytokines. This receptor binds to dsRNA molecules produced during human cytomegalovirus (HCMV) replication. TLR7 senses viral single-stranded RNA (ssRNA) in endosomes, and it can interact with endogenous RNAs. We determined the genotype distribution of single-nucleotide polymorphisms (SNPs) within the TLR3 and TLR7 genes in children with HCMV infection and the relationship between TLR polymorphisms and viral infection. We genotyped 59 children with symptomatic HCMV infection and 78 healthy individuals for SNPs in the TLR3 (rs3775290, c.1377C>T, F459F; rs3775291, c.1234C>T, L412F; rs3775296, c.-7C>A) and TLR7 (rs179008, c.32A>T, Q11L; rs5741880, c.3+1716G>T) genes. SNP genotyping was performed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and capillary electrophoresis. The HCMV DNA load was quantified by real-time PCR. We found an increased frequency of the heterozygous genotype TLR3 L412F in children with HCMV infection compared with uninfected cases. In individuals with a mutation present in at least one allele of the L412F SNP, an increased risk of HCMV disease was found, and this result remained highly significant after Bonferroni's correction for multiple testing (Pc < 0.001). The heterozygous genotype of this SNP was associated with the increased risk of HCMV disease in an adjusted model that included the HCMV DNA copy number in whole blood and urine (P < 0.001 and P = 0.008, respectively). Moreover, those with a heterozygous genotype of rs3775296 showed an increased relative risk of HCMV infection (P = 0.042), but this association did not reach statistical significance after correction for multiple testing. In contrast, the rs3775290 SNP of TLR3 and TLR7 SNPs were not related to viral infection. A moderate linkage disequilibrium (LD) was observed between the SNPs rs3775291 and rs3775296 (r2 = 0.514). We suggest that the L412F polymorphism in the TLR3 gene could be a genetic risk factor for the development of HCMV disease.

The phenomena of stabilization and flocculation through the addition of polymer is widely used in many branches of industry, e.g., agriculture. Due to the high strength of intermolecular bonding, the polymers are used as an additive to control the process of soil erosion. Flocculants strengthen the soil cohesion, which limits the transport of sediments and thus the process of soil structure degradation. Also, the presence of polymers affects the increase of water infiltration into the soil and dissolved substances, including toxic compounds. Therefore, the presence of soil flocculants may influence the occurrence of heavy metal accumulation. The aim of the study was to investigate the influence of the presence of cationic polyacrylamide on lead(II) ion adsorption onto the surface of montmorillonite. The effect of cationic group content in the polymeric macromolecules, the addition order of individual adsorbates, and the lead(II) ion concentration were also determined.

Toll-like receptor 9 (TLR9) recognizes non-methylated viral CpG-containing DNA and serves as a pattern recognition receptor that signals the presence of human cytomegalovirus (HCMV). Here, we present the genotype distribution of single-nucleotide polymorphisms (SNPs) of the TLR9 gene in infants and the relationship between TLR9 polymorphisms and HCMV infection. Four polymorphisms (-1237T/C, rs5743836; -1486T/C, rs187084; 1174G/A, rs352139; and 2848C/T, rs352140) in the TLR9 gene were genotyped in 72 infants with symptomatic HCMV infection and 70 healthy individuals. SNP genotyping was performed by using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Digested fragments were separated and identified by capillary electrophoresis. The HCMV DNA copy number was measured by a quantitative real-time PCR assay. We found an increased frequency of heterozygous genotypes TLR9 -1486T/C and 2848C/T in infants with HCMV infection compared with uninfected cases. Heterozygous variants of these two SNPs increased the risk of HCMV disease in children (P = 0.044 and P = 0.029, respectively). In infants with a mutation present in at least one allele of -1486T/C and 2848C/T SNPs, a trend towards increased risk of cytomegaly was confirmed after Bonferroni's correction for multiple testing (Pc = 0.063). The rs352139 GG genotype showed a significantly reduced relative risk for HCMV infection (Pc = 0.006). In contrast, the -1237T/C SNP was not related to viral infection. We found no evidence for linkage disequilibrium with the four examined TLR9 SNPs. The findings suggest that the TLR9 -1486T/C and 2848C/T polymorphisms could be a genetic risk factor for the development of HCMV disease.

The effects of type and content of polymer functional groups on the adsorption mechanism on the chromium (III) oxide surface were studied. Both synthetic [poly(acrylic acid) (PAA), anionic polyacrylamide (PAM), poly(aspartic acid) (ASP), block co-polymer of ASP with poly(ethylene glycol) (ASP-b-PEG)] and natural [bovine serum albumin, ovalbumin, human serum albumin, bacterial polysaccharide (exopolysaccharide EPS)] polymers were applied. For this purpose, adsorption, surface charge, zeta potential and stability measurements were carried out. The largest adsorption was found for the ASP-b-PEG (synthetic polymer) and EPS (natural polymer). The most effective destabilizers for Cr 2 O 3 removal from the aqueous suspension were PAA 240,000 and ASP 6800.

In this study, we compared the adsorption of methionine, cysteine and cystine at the mercury/chlorate (VII) interface. Changes in the surface tension with the potential of the zero charge γ z and relative surface excess Γ' of methionine, cysteine and cystine as a function of their concentration indicate that the adsorption of the studied amino acids increases in the order of methionine > cystine > cysteine. For all the systems examined, linear dependences ln[×(1–Θ)/Θ = f(Θ)] (Frumkin isotherm) and ln (Γ/c) = f(Γ') (virial isotherm) were obtained. Changes in the adsorption parameters as a function of the supporting electrolyte concentration indicate the competitive adsorption of amino acids and ClO 4 − ions and electrostatic interactions between the water dipoles and adsorbates in the double layer.

The main subject of this paper is to introduce the most significant values of business-to-business relationship marketing. The attention is particularly paid to mutual value creation, long-term co-operation, loyalty and customer retention due to the most fundamental buyer-seller rela-tionships based on trust. Moreover, the relationship marketing, business-to-business co-operation in the context of basic marketing relationships are described. The relationship marketing, regard-ing to Gummesson’s definition, is seen in the context of relationships, networks and interaction. This approach underlines the meaning of relationship management, which aims at creation, de-velopment, and maintenance of network in which the company succeeds. Moreover, there is a strong need for interaction between buyers and sellers due to produce and sell the goods and ser-vices with impact on direct, personal communication. The relationship marketing is the value it-self in the process of interaction between parties involved, as it provides the rule of equity be-tween co-operating companies of more winning and less loosing situations. This paper highlights the value of co-operation, however does not exclude competition. Co-operation and competition are treated inseparably in business. There is also a concern for activity and taking responsibility by parties involved described as well as the importance of relationship and service values instead of bureaucratic-legal values stressed. Customers need to be in focus, respected, treated individually as they are the purpose of value creation in the business-to-business relationship marketing.