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The interactions of metal ions with fulvic acids were investigated from the point of view of the thermodynamic aspects of complexation as well as the size and charge of the formed complexes. Thermodynamic aspects were studied by means of isothermal titration calorimetry. Particle size distribution was determined by the method of dynamic light scattering and charge by the measurement of zeta potential. Complexation resulted in changes in particle size and charge. The particle size distribution was trimodal for fulvic acids and bimodal for fulvic complexes with calcium and magnesium, while copper–fulvic complexes had only one size fraction. The compensation of the negative charge of carboxylic and phenolic functional groups by positively charged metal ions resulted in an increase in zeta potential which became closer to zero in the case of copper–fulvic complexes. However, all metal–humic complexes behaved as colloidally unstable, which resulted in visually observable sedimentation. Calorimetric measurements provided positive values for changes in enthalpy, which indicated endothermic processes. In contrast, quantum chemical calculations as well as experiments with model compounds provided negative values indicating exothermic processes. Changes in Gibbs energy were determined as negative and changes in entropy as positive., Interakce fulvinových kyselin s kovovými ionty jsou sledovány pomocí titrační kalorimetrie, která poskytla základní fyzikálně chemické charakteristiky. Doplněna byla stanovením distribuce velikosti částic a zeta potenciálu.

In recent years, nanoparticles have emerged as an important player in a broad range of applications, especially thanks to recent advances in their synthesis. The silver and copper nanoparticles are often used due to their antibacterial and fungicidal activities, and this article presents the results of the nanoparticle synthesis using electrical glow discharge generated directly in a volume of their salt solutions. Therefore, there is no influence of air (i.e. reactive nitrogen species) as it is usual in other commonly used approaches. Nanoparticles were prepared under various experimental conditions, and they were characterized by ultraviolet/visible spectrometry, dynamic light scattering, X-ray photoelectron spectroscopy, and high-resolution scanning electron microscopy. Particles were produced without any surfactant or stabilizing agent, and some of them showed higher resistance against agglomeration during their short-term (days) storage. The nanoparticle formation mechanism was confirmed by the fast camera imaging. Thus, the developed approach can be applied for simple environmentally friendly nanoparticle production for various applications., IV posledních letech je pozorován prudký nárůst aplikací nanočástic, a to zejména díky progresu v jejich přípravě. Stříbrné a měděné nanočástice jsou často užívány pro svou antimikrobiální a antimykotickou aktivitu. Článek prezentuje syntézu těchto annočástic pomocí plazmatu generovaného přímo ve vodném roztoku anorganických solí, tedy bez přístupu vzduchu. Proces přípravy probíhal za různých podmínek. K charakterizaci nanočástic bylo využito UVS-VIS spektrometrie, dynamického rozptylu světla, rentgenovské fotoelektronové spektormetrie avysoce rozlišující skenovací elektronové mikroskopie. Částice byly připravovány bez použití surfaktantů nebo jiných stabilizačních činidel, a některé z nich nevykazovaly po řadu dní aglomerační tendence. Mechanismus vzniku nanočástic byl potvrzen s využitím snímání vysokorychlostní kamerou. Použitý přístup představuje efektivní a přírodě přátelský postup přípravy kovových nanočástic.

Biochar represents a stable form of carbon-rich organic material produced by the pyrolysis of various biomass residues. It has the potential to stabilize organic carbon in the soil and improve soil fertility, water retention, and enhance plant growth. Despite its potential, there is limited information on the mutual relation of biochar texture with its physicochemical characteristics, morphology, and the content of organic matter. For these reasons, we studied three biochar samples with potential use in agriculture as soil supplements (NovoCarbo, Sonnenerde, Bi-ouhel.cz). Our experimental approach performed on the individual sieved fraction of studied biochars (<0.5; 0.5–2.0; 2.0–4.0 and >4.0 mm) confirmed the importance of a selection of optimal source biomass material as the content of lignin, cellulose, and hemicellulose, together with the conditions of pyrolysis (temperature of pyrolysis), play a crucial role in the managing of the properties of produced biochar. Agronomically more stable biochars containing a higher con-tent of organic matter and organic carbon, with alkaline pH response and well-developed aro-matic porous structure, could be produced from lignin-based biomass residues at higher pyroly-sis temperatures, which is an important finding taking into account the possible utilization of biochar in soils as a soil conditioner.

Production of polyhydroxyalkanoates (PHA), microbial biopolyesters, employing extremophilic microorganisms is a very promising concept relying on robustness of such organisms against microbial contamination, which provides numerous economic and technological benefits. In this work, we took advantage of the natural susceptibility of halophilic and thermophilic PHA producers to hypotonic lysis and we developed a simple and robust approach enabling effective isolation of PHA materials from microbial cells. The method is based on the exposition of microbial cells to hypotonic conditions induced by the diluted solution of sodium dodecyl sulfate (SDS) at elevated temperatures. Such conditions lead to disruption of the cells and release of PHA granules. Moreover, SDS, apart from its cell-disruptive function, also solubilizes hydrophobic components, which would otherwise contaminate PHA materials. The purity of obtained materials, as well as the yields of recovery, reach high values (values of purity higher than 99 wt.%, yields close to 1). Furthermore, we also focused on the removal of SDS from wastewater. The simple, inexpensive, and safe technique is based on the precipitation of SDS in the presence of KCl. The precipitate can be simply removed by decantation or centrifugation. Moreover, there is also the possibility to regenerate the SDS, which would substantially improve the economic feasibility of the process.

Films prepared from poly(3-hydroxybutyrate-co-4-hydroxybutyrate) copolymers produced by Aneurinibacillus sp. H1 using an automatic film applicator were homogeneous and had a defined thickness, which allowed a detailed study of physicochemical properties. Their properties were compared with those of a poly (3-hydroxybutyrate) homopolymer film prepared by the same procedure, which proved to be significantly more crystalline by DSC and XRD. Structural differences between samples had a major impact on their properties. With increasing 4-hydroxybutyrate content, the ductility and release rate of the model hydrophilic active ingredient increased significantly. Other observed properties, such as the release of the hydrophobic active substance, the contact angle with water and ethylene glycol, or the surface morphology and roughness, were also affected by the composition. The identified properties predetermine these copolymers for wide use in areas such as biomedicine or smart biodegradable packaging for food or cosmetics. The big advantage is the possibility of fine-tuning properties simply by changing the fermentation conditions.

A novel model of biodegradable PHA copolymer films preparation was applied to evaluate the biodegradability of various PHA copolymers and to discuss its biomedical applicability. In this study, we illustrate the potential biomaterial degradation rate affectability by manipulation of monomer composition via controlling the biosynthetic strategies. Within the experimental investigation, we have prepared two different copolymers of 3-hydroxybutyrate and 4-hydroxybutyrate-P(3HB-co-36 mol.% 4HB) and P(3HB-co-66 mol.% 4HB), by cultivating the thermophilic bacterial strain Aneurinibacillus sp. H1 and further investigated its degradability in simulated body fluids (SBFs). Both copolymers revealed faster weight reduction in synthetic gastric juice (SGJ) and artificial colonic fluid (ACF) than simple homopolymer P3HB. In addition, degradation mechanisms differed across tested polymers, according to SEM micrographs. While incubated in SGJ, samples were fragmented due to fast hydrolysis sourcing from substantially low pH, which suggest abiotic degradation as the major degradation mechanism. On the contrary, ACF incubation indicated obvious enzymatic hydrolysis. Further, no cytotoxicity of the waste fluids was observed on CaCO-2 cell line. Based on these results in combination with high production flexibility, we suggest P(3HB-co-4HB) copolymers produced by Aneurinibacillus sp. H1 as being very auspicious polymers for intestinal in vivo treatments.