Silver selenide modification of polyamide fabric

Formation of a silver selenide layer on silicone coated polyamide cloth was investigated. Fabric samples were selenized in potassium selenotrithionate (K₂SeS₂O₆) solution then treated with AgNO₃ solution. Formation of a silver selenide particle layer on the surface was confirmed by a change in appearance, X-ray diffraction, and EDX analysis. XRD revealed two phases: orthorhombic naumannite (Ag₂Se) and monoclinic selenium (Se₈). SEM showed that the fabric macrostructure and the multifilament yarn microstructure was preserved. The silver selenide particles ranged from 100 nm to more than 20 µm.      

Series of fuzzy sets

Series of fuzzy sets with weakly closed, weakly compact or compact α-levels are considered. The basic space is Banach space. The subject of this paper is investigation of infinite addition of fuzzy sets and condition when the sum of α-levels is equal to the α-level of the sum. The results in this paper complement and complete some previous results proved by the same authors in Stojaković and Stojaković [Addition and series of fuzzy sets, Fuzzy Sets and Systems 83 (1996) 341–346] for the series with compact α-levels.     

Determination of multiple pharmaceutical classes in surface and ground waters by liquid chromatography–ion trap–tandem mass spectrometry

This paper describes development, optimization and application of analytical method for determination and reliable confirmation of nineteen pharmaceuticals from different therapeutic classes (antibiotics—β-lactams, cephalosporines, sulfonamides, macrolides and tetracyclines; benzodiazepines; antiepileptics and analgoantipyretics) in surface and ground waters at ng l⁻¹ levels. Water samples were prepared using solid-phase extraction and extracts were analyzed by liquid chromatography–ion trap–tandem mass spectrometry with electrospray ionization in both positive and negative ionization mode. The efficiency of ten different SPE cartridges to extract diverse compounds from water was tested. The pH-value of the water sample, the volume of elution solvent and the sample volume were optimized. Matrix effect, especially pronounced for cephalexin and metamizole, was eliminated using matrix-matched standards. It was determined that extraction should be performed at pH ∼ 7.5, i.e. without pH adjustment, and at pH 3, depending on the analyte. Azithromycin, doxycycline and acetylsalicylic acid must be extracted in acidic environment, whereas extraction of paracetamol, ampicillin, erythromycin and metamizole should be performed without pH adjustment. Repeatability of the method was generally lower than 20%. The estimated limits of detection were in the range from 0.15 to 12.46 ng l⁻¹. The method was applied to 26 water samples for monitoring of selected drug residues. Results revealed the presence of carbamazepine (80% of water samples), azithromycin (23%), as well as trimethoprim and paracetamol (both 15%). The most striking was the false positive signal of diclofenac in every analyzed water sample. Confirmation of the positive results was performed by repeated injection of the positive sample extracts using confirmatory method with additional transitions.     

Selective Detection of Dopamine Using Glassy Carbon Electrode Modified by a Combined Electropolymerized Permselective Film of Polytyramine and Polypyrrole‐1‐propionic Acid

A sensitive and selective electrochemical method for the determination of dopamine using a combined electropolymerized permselective film of polytyramine and polypyrrole‐1‐propionic acid on a glassy carbon (GC) electrode was developed. The formation of a “layer‐by‐layer” film has allowed for selective detection of dopamine in the presence of 3,4‐dihydroxyphenylalanine (L‐DOPA), DOPAC, ascorbic acid, uric acid, epinephrine and norepinephrine. The modified electrodes exhibited a detection limit of 100 nM with linearity ranging from 5×10^?6 to 5×10^?5 M. No cleaning step was required during the course of repeated measurement.     

Supersolid phase induced by correlated hopping in spin-1/2 frustrated quantum magnets

We show that correlated hopping of triplets, which is often the dominant source of kinetic energy in dimer-based frustrated quantum magnets, produces a remarkably strong tendency to form supersolid phases in a magnetic field. These phases are characterized by simultaneous modulation and ordering of the longitudinal and transverse magnetization, respectively. Using quantum Monte Carlo and a semiclassical approach for an effective hard-core boson model with nearest-neighbor repulsion on a square lattice, we prove, in particular, that a supersolid phase can exist even if the repulsion is not strong enough to stabilize an insulating phase at half-filling. Experimental implications for frustrated quantum antiferromagnets in a magnetic field at zero and finite temperature are discussed.     

Quadrupolar phases of the s=1 bilinear-biquadratic Heisenberg model on the triangular lattice

Using mean-field theory, exact diagonalizations, and SU(3) flavor theory, we have precisely mapped out the phase diagram of the S = 1 bilinear-biquadratic Heisenberg model on the triangular lattice in a magnetic field, with emphasis on the quadrupolar phases and their excitations. In particular, we show that ferroquadrupolar order can coexist with short-range helical magnetic order, and that the antiferroquadrupolar phase is characterized by a remarkable 2/3 magnetization plateau, in which one site per triangle retains quadrupolar order while the other two are polarized along the field. Implications for actual S=1 magnets are discussed.     

Spontaneous plaquette formation in the SU(4) spin-orbital ladder

The low-energy properties of the SU(4) spin-orbital model on a two-leg ladder are studied by a variety of analytical and numerical techniques. As in the case of SU(2) models, there is a singlet-multiplet gap in the spectrum, but the ground state is twofold degenerate. An interpretation in terms of SU(4)-singlet plaquettes is proposed. The implications for general two-dimensional lattices are outlined.     

Speciation of aluminium in tea infusions by use of SEC and FPLC with ICP–OES and ES–MS–MS detection

Speciation of Al in tea infusions was studied by size exclusion chromatography (SEC) and anion-exchange fast protein liquid chromatography (FPLC). Fractions were collected throughout the chromatographic separations and Al was determined “off line” by inductively coupled plasma optical emission spectroscopy (ICP–OES). Black, green, and red tea samples were investigated. The total concentration of Al in tea infusions was determined by ICP–OES and ranged between 0.5 and 4 mg dm⁻³. The pH of tea infusions ranged between 5.3 and 5.5. Data from SEC–ICP–OES analysis indicated that 10–35% of total Al in tea infusions was eluted at a retention volume corresponding to a molecular mass of approximately 3800 Da. The remaining Al was adsorbed on the column resin. The same tea infusions were also analysed by anion-exchange FPLC–ICP–OES. It was found experimentally that the same percentage of total Al as from the SEC column was eluted at a retention volume that corresponded to negatively charged Al-citrate. The remaining Al was adsorbed on the column resin. Identification of Al-binding ligands eluting under the chromatographic peak was performed by electrospray ionisation tandem mass spectrometry (ES–MS–MS) analysis. It was proven that ionic Al species in tea infusions (10–35% of the total Al) corresponded to negatively charged Al-citrate. The remaining species that was adsorbed on the SEC or FPLC columns was most probably bound to phenolic compounds. Speciation of Al in tea with milk or lemon was also studied. Results for tea with milk indicated that Al-citrate was not transformed and that approximately 60% of total Al was transformed into high-molecular-mass Al species. This fraction was subjected to sodium dodecyl sulfonate polyacryl gel electrophoresis (SDS–PAGE). The results indicated that Al was occluded by milk proteins (mostly caseins). When citric acid was added to tea infusions the percentage of negatively charged Al-citrate remained either the same or increased to 40% of total Al.     

The chemical speciation of aluminium in human serum

Chemical speciation of aluminium in the low molecular mass (LMM) and high molecular mass (HMM) fractions of human serum is discussed. A critical review of the literature on different analytical procedures described for the speciation of aluminium in human serum samples is presented here. The methodologies, the experimental and instrumental requirements and the ability of the reported analytical procedures for identification of HMM and LMM aluminium species in human serum are examined in detail. Non-chromatographic separations coupled to electrothermal atomic absorption spectrometry for aluminium detection are compared with chromatographic techniques (size exclusion chromatography, anion exchange chromatography and fast protein liquid chromatography) coupled to ETAAS or inductively coupled plasma mass spectrometry (ICP-MS) detection for Al-HMM species investigations. Studies and techniques reported for Al-LMM compounds are also summarised, both for healthy volunteers and dialysis patients. On the basis of the knowledge obtained from the application of the developed analytical procedures to real serum analysis, it has been demonstrated that most of Al in human serum is bound to Al-transferrin, while the LMM-Al fraction (10-20% of total Al) mainly contains Al-citrate, Al-phosphate and ternary Al-citrate-phosphate complexes.