Synthetic dyes or colorants are key chemicals for various industries producing textiles, food, cosmetics, pharmaceutics, printer inks, leather, and plastics. Nowadays, the textile industry is the major consumer of dyes. The mass of synthetic colorants used by this industry is estimated at the level of 1 ÷ 3 × 10⁵ tons, in comparison with the total annual consumption of around 7 × 10⁵ tons worldwide. Synthetic dyes are relatively easy to detect but difficult to eliminate from wastewater and surface water ecosystems because of their aromatic chemical structure. It should be highlighted that the relatively high stability of synthetic dyes leads to health and ecological concerns due to their toxic, mutagenic, and carcinogenic nature. Currently, removal of such chemicals from wastewater involves various techniques, including flocculation/coagulation, precipitation, photocatalytic degradation, biological oxidation, ion exchange, adsorption, and membrane filtration. In this review, a number of classical and modern technologies for synthetic dye removal from industry-originated wastewater were summarized and discussed. There is an increasing interest in the application of waste organic materials (e.g., compounds extracted from orange bagasse, fungus biosorbent, or green algal biomasses) as effective, low-cost, and ecologically friendly sorbents. Moreover, a number of dye removal processes are based on newly discovered carbon nanomaterials (carbon nanotubes and graphene as well as their derivatives).

In the latest literature search, the technology based on graphite oxide (GO) nanomaterials exhibits a great potential in many aspects of wastewater treatment involving adsorption, photocatalysis, disinfection and membrane process. In this study experimental data involving the carbon element in different forms such as active carbon (AC), graphite and graphene oxide (GO) applied as the active reagents in wastewater treatment are summarized and discussed. The first step was to characterize the aforementioned carbon materials and nanoparticles using various complementary techniques. These include optical microscopy, scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), Raman spectrophotometry and zeta potential measurements. The second issue was to design the relatively simple experiment enabling us to observe the physicochemical and biological effects of carbon nanoparticles in the presence of sewage water and/or active sludge. Obtained experimental data have been inspected using univariate and multivariate (principal component analysis, PCA) approaches confirming the complex interaction of GO nanoparticles with microorganisms that are present in activated sludge. This experiment enabled the collection of an initial data set to design different large scale investigations focusing on active nanoparticles affecting wastewater purification. PCA calculations clearly revealed that GO strongly affects the wastewater technological processes investigated. It is hoped that the described results will allow the design of smart environmental protection systems in the future.

The observed increase in the diversity and level of pollutant content in the water environment forces the development of more effective technologies for their removal. Using nanomaterials in water and wastewater treatment offers numerous opportunities to remove organic and inorganic contaminants that are hardly removable in conventional processes. In this group, carbon-based nanomaterials, mainly carbon nanotubes (CNTs), graphene (Gr), and graphene oxide (GO), are very popular. This review aims to present the directions and diversity of applications of carbon-based nanomaterials (CNMs) in water and wastewater technology, as well as the challenges and environmental dangers that new solutions entail. Authors also present the results of the research on the changes in properties of GO produced in the laboratory as water suspension and a freeze-dried product over time. The results confirm the significant influence of the form of graphene oxide and its storage time on the structural properties, hydrophilicity, and stability of GO. Therefore, they should be considered when selecting an adsorbent or reaction catalyst in environmental applications for developing new greener and sustainable methods of treatment and purification, which use fewer reagents and release safer products.

The main goal of this review is to summarize practical approaches concerning the application of microfluidic systems for the analysis of various biomarkers and pollutants, as well as microbes, in water and wastewater matrixes. This problem involves multidisciplinary expertise combining research knowledge from various areas, including wet chemistry, biochemistry, physical chemistry, molecular biology, genetics, signal processing, microelectronics material science, and separation science. It has been documented that fairly primitive but fast and inexpensive screening methods involving paper-based analytical devices (PADs) and micro total analytical systems (μTAS) can be considered as serious alternatives to their more advanced counterparts such as GC, HPLC, and capillary electrophoresis coupled to various sophisticated detectors (e.g., multiwavelength spectrophotometers such as UV-Vis/DAD and mass spectrometers). The main advantage of PAD- and μTAS-driven technology is that such sensing devices may work under on-site and real-time conditions and measure a number of physical parameters and chemical factors simultaneously. Moreover, hybrid miniaturized analytical systems may combine sensing and data acquisition modules with common mobile phones and electronic devices working with global positioning systems and communicating through the Internet.

The main goal of this experimental work is screening of different natural and synthetic nanomaterials and biopolymers that may improve elimination of stable micropollutants from water phase. In this work, as a target chemical acting as the micropollutant molecule, the Brilliant Blue (BB) dye was selected. We tested different active matrices dispersed in water phase including activated carbon (AC), lyophilized graphene oxide (GO), β-cyclodextrin (CD), raw dandelion pappus (DP), microcrystalline cellulose(MC), and raw pine pollen (PP), as well as two types of Egyptian Blue mineral pigments (EB1 and EB2). Graphene oxide and Egyptian Blue nanomaterials were synthesized in our laboratory. We investigated potential application of such nanoparticles and biopolymer conglomerates as additives that may tune the activated sludge (AS) microorganisms or duckweed water plant (DW) and increase efficiency of micropollutants removal from wastewater. Studied nanomaterials/biopolymers were used in two different experimental modes involving real activated sludge microorganisms (24 h experiment) as well as duckweed plant (16 day experiment). Quantitative data of BB were obtained using microfluidic type device based on micro-TLC plate. This approach enabled direct determination of target component without sample pre-treatment like pre-concentration or pre-purification. Within single analytical run calibration line, retention standard spots (methyl red) and multiple samples were analyzed simultaneously. Due to the multivariate nature of these experiments, quantitative data were explored with chemometric tools including AHC (agglomerative hierarchical clustering), PCA (principal component analysis), and FA (factor analysis). Experimental data and multivariate calculations revealed that BB is strongly resistant on biodegradation, however, inclusion complexes formation with β-cyclodextrinmay induce degradation of this dye in the presence of duckweed. It is hoped that results of our experimental work can be used for designing of future experiments for fast screening of different additives and improvement of technological processes, focusing on purification of sewage and water from micropollutants.

We report the results of experimental work focusing on host-guest supramolecular complex creation between macrocyclic compound (β-cyclodextrin) and 1-acenaphthenol enantiomers (racemic mixture) in liquid phase composed of 35% acetonitrile in water (v/v) at different temperatures ranging from 0 to 90 °C. Experimental setup involved several analytical protocols based on classical non-forced flow planar chromatography (RP-18 TLC plates), micro-TLC (RP-18 W HPTLC plates), column chromatography (HPLC with C-18 and C-30 stationary phases), as well as UV-Vis spectrophotometry and optical microscopy. It has been found that under various planar chromatographic conditions (stationary plates type, chamber shape and volume, development mode, and saturation) non-typical retention properties (extremely high retention) of 1-acenaphthenol at subambient temperatures can be observed. To our knowledge, reported experimental results are in opposition to currently described retention models based on column chromatographic investigation of host-guest complexes (where in case of strong interaction of given analyte with macrocyclic mobile phases additive, which itself is non strongly retarded by stationary phase—close to the retention of dead volume marker, the retention of target compounds is shortened at low temperatures). To explain this TLC phenomenon that may have in our opinion a number of practical applications, especially for selective high throughput separation involving microchromatographic and/or microfluidic devices as well fractionation and extraction protocols (using, e.g., bar extraction systems), several experiments were conducted focusing on (i) acenaphthenol chromatography under different instrumental conditions, (ii) cyclodextrin retention measured as analyte or mobile phase additive, (iii) plate development time under different mobile phases and temperature settings, (iv) various column chromatographic conditions including C-30 and two C-18 stationary phases, (v) UV-Vis spectrophotometry, and (vi) microscopy inspection of precipitated CD-acenaphthenol crystals. Analysis of collected data has revealed that the most probable reasons for TLC retention behavior of 1-acenaphthenol under β-cyclodextrin additive conditions can be associated with (i) solubility changes of created host-guest complex, (ii) kinetics of solid complex precipitation, and (iii) differences in analysis time between planar and column chromatography. Because precipitation phenomenon may have a massive impact on analytes quantification involving macrocycles as the mobile phase additives, our previously reported data concerning a number of low-molecular compounds (mainly steroids and non steroidal endocrine disrupting chemicals) using HPLC methodology based on binary mobile phases without and with β-cyclodextrin and its hydroxypropyl derivative were re-examined and results discussed. Considering these data and the whole data set reported presently, the enhanced model of chromatographic retention driven by host-guest interaction was proposed.