Course Of Reaction Research Articles

CALCULATION OF THERMODYNAMIC TEMPERATURES OF CHEMICAL REACTIONS OF STEPWISE MANGANESE REDUCTION PROCESS FROM ITS DIOXIDE BY CO GAS AND GASIFICATION OF SOLID CARBON BY DEGREES OF CHEMICAL AFFINITY OF SUBSTANCES TO OXYGEN

The results of a thermodynamic analysis of the course of chemical reactions of the stepwise reduction of manganese from its dioxide by CO gas and the gasification reaction of solid carbon (Bella-Boudoir) are presented. The goals of the work are to obtain eigenexpressions for calculating the numerical values of the Gibbs free energy depending on temperature using tabulated values of the standard enthalpies of formation and entropies of inorganic substances, as well as to construct graphical dependences of the Gibbs energy on temperature using formulas from literary sources and obtained expressions. Numerical values of the boundary temperatures are obtained above which the chemical reactions of the stepwise reduction of manganese from its dioxide by CO gas and the chemical reaction of gasification of solid carbon (Bella-Boudoir) can or cannot thermodynamically proceed. Considering the complete coincidence of the obtained data on the own (obtained) expressions using two (direct and indirect) methods, it is possible to consider with a significant degree of probability the numerical values of the boundary temperature for the reactions of stepwise reduction of manganese from its dioxide and gasification of solid carbon as reliable, which indicates the possibility of the reduction of Mn2O3 from MnO2, Mn3O4 from Mn2O3 and MnO from Mn3O4 by CO gas, the Bell-Boudoir reaction and the impossibility of the reduction of manganese from MnO by CO gas at the temperatures of the actual process in reduction furnaces. This also confirms that CO gas is not a manganese reducer at the last stage of stepwise reduction of MnO according to scheme (B), refuting any theories and assumptions about the possibility of reducing Mn from MnO by CO gas.

Inverse Electron Demand Diels-Alder Reaction of Pyrazines with 2,5-Norbornadiene as Acetylene Precursor

Herein, we report the reaction of pyrazines with 2,5-norbornadiene, an acetylene precursor, as a cascade of Diels-Alder reactions yielding substituted pyridines. In contrast to the known examples of intermolecular Diels-Alder type reaction of pyrazines with acetylene, which usually leads to a mixture of products, in our case the formation of a single isomer was observed. The proposed approach allows the conversion of pyrazines with different types of substitution, except those containing methyl and amino donor groups, to pyridines. In addition, highly functionalized aminonicotic esters were obtained, which can be used for the synthesis of bioactive compounds. An unusual course of the Diels-Alder reaction was found in the case of tetrasubstituted pyrazines, which cleave organic nitriles instead of HCN. Quantum-chemical modeling of possible transition states showed that this Diels-Alder reaction proceeds via cycloaddition of 2,5-norbornadiene to pyrazine with sequential elimination of HCN and cyclopentadene; the reaction pathway including initial formation of acetylene from norbornadiene and subsequent Diels-Alder reaction with the acetylene was rejected as kinetically unfavorable.

Enantioselective Synthesis of vic-Aminoalcohol Derivatives by Nickel-Catalyzed Reductive Coupling of Aldehydes with Protected Amino-pentadienoates.

A VAPOL-derived phosphoramidite ligand is uniquely effective at reverting the regiochemical course of nickel-catalyzed reactions of aldehydes with carbamate-protected 5-amino-2,4-pentadienoates as "push/pull" dienes; the ensuing carbonyl α-amino-homoallylation reaction affords anti-configured vic-aminoalcohol derivatives in good yields with high optical purity. The reductive coupling is conveniently performed with a bench-stable Ni(0) precatalyst and Et3B as the promoter.

Observation of an order change during the course of a reaction in a kinetic study of the reduction of trans-dicyanodibromoaurate(III) by octacyanotungstate(IV) in an acidic medium

AbstractThe reduction of dibromodicyanoaurate(III) ion by octacyanotungstate(IV) ions was studied under near stoichiometric conditions in an acidic medium. An order change occurred during the course of the reaction. The reaction was first order in Au(CN)2(Br)2– and second order in W(CN)84– for the first half-life, but after ca. 60% conversion became first order in both reactants. The order change is ascribed to two different AuII intermediates that form during the reaction course. A third order rate constant of k3 = 7.80 × 105 M−2 min−1 and a second order rate constant of k2 = 108 M−1 min−1 was found at [H+] = 1.633 × 10–3 M, an ionic strength of I = 0.11 M (NaBr) and at 25.0 ± 0.1 °C for the reaction. The reaction rate decreases with increasing [H+] in the reaction mixture at low pH and an experimental pKa of 1.80 ± 0.03 was found at 25.0 ± 0.1 °C for the deprotonation of HW(CN)83–. The reaction rate is independent of [Br−] and decrease with addition of W(CN)83– in the reaction mixture. Activation parameters have been obtained by a least-squares fit of the temperature data directly to the Eyring equation. Graphical abstract

Force-Assisted Orbital Crossing in Mechanochemical Oxirane Ring Opening.

Polymer mechanochemistry induces chemical reactivity by applying a directed force, which can lead to unexpected reaction mechanisms. Strained cyclic molecules are often used in force-sensitive motifs because of the strong force coupling of ring-opening reactions. In this computational study, the force dependence of the ring-opening reactions of oxirane will be investigated. Density functional theory and multireference methods were used to investigate the electronic character of both symmetry-allowed and symmetry-forbidden reactions. In the latter case, an orbital crossing occurs during the reaction course, forcing the Woodward-Hoffmann-forbidden reaction to proceed via a diradical pathway. The performance of broken-symmetry density functional theory is evaluated and compares well to high-accuracy CASPT2, MRCI, and ic-MRCC computations. Due to the high ring strain, the barrier heights of both ring-opening reactions are steeply reduced by the application of an external force. Furthermore, the use of unsaturated linkers was shown to yield a significant reduction of the barrier heights, explaining previous experimental findings. Finally, we show through analysis of the PES topology how the external force transforms characteristic points such as saddle points and bifurcations, providing insights into force-dependent mechanism changes.

From In Situ Monitoring to Better Understanding of the Suzuki‐Miyaura Cross Coupling in the Solid State

AbstractEffects of various Additives, Base, Catalyst, as well as substrates on the mechanochemically‐induced Suzuki‐Miyaura reaction have been studied. In situ Raman monitoring of the solid‐state reactions gave a detailed view of the reaction course and allowed a direct comparison of the time‐resolved product formation. The acquired knowledge allows in‐depth understanding of the reaction, especially the action of the catalyst in presence of diverse chemicals, leading to the more efficient cross coupling reactions in the solid state.

Oxoammonium-Catalyzed Ether Oxidation via Hydride Abstraction: Methodology Development and Mechanistic Investigation Using Paramagnetic Relaxation Enhancement NMR.

Hydride abstraction represents a promising yet underexplored approach in the functionalization of C-H bonds. In this work, we report the oxidation of α-C-H bonds of ethers via oxoammonium catalysis using 3-chloroperbenzoic acid (mCPBA) as the terminal chemical oxidant or by means of electrochemistry. Mechanistic studies revealed intricate equilibria and interconversion events between various catalytic intermediates in the presence of mCPBA, which alone however was incompetent to drive catalytic turnover. The addition of a small amount of strong acid HNTf2 or weakly coordinating salt NaSbF6 turned on catalytic turnover and promoted ether oxidation with excellent efficiency. NMR experiments leveraging paramagnetic relaxation enhancement effect allowed for quantification of open-shell catalytic intermediates in real time during the reaction course, which aided the identification of catalyst resting states and elucidation of reaction mechanisms.

Photochemistry with Plane-Polarized Light: Controlling Selectivity of a Photochemical Rearrangement.

Over the past 50 years, a principal approach to controlling conventional photochemical reactions has relied on imposing geometric constraints on reactant or transition state via conducting photochemistry in the organized or constraining media. Herein, we describe a fundamentally different approach to affect the course of photochemical reactions (photochemical rearrangements) by utilizing spatially selective excitation of specific electronic transitions with plane-polarized light in the reactant molecules uniformly aligned in the nematic liquid crystal phase. In particular, we focused on the Type B enone rearrangement of 4,4-diarylcyclohexenones - one of the most common photochemical rearrangements. We demonstrated that the aryl migratory aptitude in this reaction was attenuated in response to changing an angle between the polarization plane of the incident light and the alignment direction of the nematic liquid crystal, with the enhanced aryl migration achieved when the polarization plane coincided with the transition dipole moment leading to the excited state responsible for this migration. The spatially-selective initial excitation therefore was overruling the electronic factors responsible for the relative ratio of the two alternative photoproducts. The experimental findings were further supported by the results of a computational study. This work showcases a new fundamental paradigm in controlling photochemical reactivity and selectivity of photoreactions.

Unexpected Course of Reaction Between (1E,3E)-1,4-Dinitro-1,3-butadiene and N-Methyl Azomethine Ylide-A Comprehensive Experimental and Quantum-Chemical Study.

In recent times, interest in the chemistry of conjugated nitrodienes is still significantly increasing. In particular, the application of these compounds as building blocks to obtain heterocycles is a popular object of research. Therefore, in continuation of our research devoted to the topic of conjugated nitrodienes, experimental and quantum-chemical studies of a cycloaddition reaction between (1E,3E)-1,4-dinitro-1,3-butadiene and N-methyl azomethine ylide have been investigated. The computational results present that the tested reaction is realized through a pdr-type polar mechanism. In turn, the experimental study shows that in a course of this cycloaddition, only one reaction product in the form of 1-methyl-3-(trans-2-nitrovinyl)-Δ3-pyrroline is created. The constitution of this compound has been confirmed via spectroscopic methods. Finally, ADME analysis indicated that the synthesized Δ3-pyrroline exhibits biological potential, and it is a good drug candidate according to Lipinski, Veber and Egan rules. Nevertheless, PASS simulation showed that the compound exhibits weak antimicrobial, inhibitory and antagonist properties. Preliminary in silico research shows that although the obtained Δ3-pyrroline is not a good candidate for a drug, the presence of a nitrovinyl moiety in its structure indicates that the compound is an initial basis for further modifications.

Effect of Nucleophile Deprotonation on SuFEx: Synthesis of Sulfonamides

In a quest for efficient SuFEx-type transformations we studied reactions of amines with 4-fluorobenzenesulfonyl fluoride. The substrate may react by fluoride substitution at the aromatic ring (SNAr) and at the sulfonyl group (SuFEx). Analysis of the reaction course revealed that deprotonation of N-nucleophile controls the reaction course: neutral amines in DMF attack at the aromatic ring, whereas amine anions, generated in equilibrium with LiHMDS in toluene, favor sulfonyl substitution. Using the base-promoted conditions we synthesized a set of substituted sulfonamides in high yields.

Sustainable C-H Methylation Employing Dimethyl Carbonate.

The use of CO2 and CO2-derived chemicals offers society sustainable and biocompatible chemistry for a variety of applications, ranging from materials to medicines. In this context, dimethyl carbonate (DMC) stands out owing to its low toxicity, high biodegradability, tunable reactivity, and sustainable production. Further, the ability of DMC to act as an ambient electrophile at varied temperatures and reaction conditions in order to produce methoxycarbonylated (via BAC2) and methylated products (via BAL2) is very promising. While the methylation of hetero-H (N-, O-, and S-methylation) with DMC is established and well-reviewed, the C-H methylation reaction with DMC is limited, and there is no specific literature detailing the C-methylation reaction using DMC, creating new opportunities as well as challenges in the same domain. In this context, the present perspective focuses on the new breakthroughs, recent advances, and trends in C-H methylation reactions employing DMC. A critical analysis of the mechanistic course of reactions under each category was undertaken. We believe this timely perspective will offer an in-depth analysis of existing literature with critical remarks, which will certainly inspire fellow researchers across disciplines to understand and pursue cutting-edge research in the area of C-H methylation (alkylation) using DMC and related organic carbonates.

Features of the microbiome of burial soils

Introduction. On the territory of the Russian Federation, as well as worldwide, a large amount of space is allocated for burials. The soils found in the burial areas have their own characteristics. In the scientific literature there is a few works devoted to the problem of hygienic assessment of cemeteries from the point of view of their impact on the environment, as well as on the population living next to necrosols or working on them. Depending on the chemical and biological effects, the microbial composition of the soil changes. This process is influenced by many factors, including humidity, the initial content of organic and mineral substances, level of acidity, structure of the soil and peculiarities of the course of intra-soil gas-phase reactions. The key participants in the decomposition of organic material are bacteria and fungi, the diversity and dynamics of which directly depend on the degree of soil contamination with pollutants. The purpose of this study was to analyze the microbiota of cemetery soil in its various layers. Materials and methods. The cemeteries of Moscow (NikoloKhovanskoye, Nikolo-Arkhangelskoye, Perepechenskoye), Moscow (Mytishchenskoye, Domodedovo), Tula (Municipal Cemetery No. 1 of the Municipal State Enterprise of the Municipal Formation of the City of Tula Combine of Specialized Services), Kursk (old city cemetery Kurchatov), Krasnoyarsk (Zheleznogorsk) regions and Altai (Yarovoye) Krais were selected as research objects for assessing the microbiome of soils. Results. The most common bacterial pathogens were found to be Enterococcus spp. (81%), Bacillus spp. (75%) and E. coli (45.1%). Mushrooms of Penicillium spp.. were isolated from 61% of the samples. The revealed microbiota profiles of the samples of the studied cemetery soils reflect the microbial composition of humans, which allows substantiating the main methods and algorithm for identifying decomposition processes depending on the time frame of burials. Limitations. The limitation of the study is due to the risk of contact with cemetery soil was not assessed, since not all genera of isolated microorganisms could be identified by their biochemical properties. Conclusion. Studies conducted in cemetery areas have shown how diverse the soil microbiome is in burial sites and varies depending on the depth of sampling. The microbiota profiles of cemetery soil samples identified during the study reflect the lifetime microbial composition of the human body, which makes it possible to substantiate approaches to identifying decomposition processes depending on the time frame of burials.

Crystal Structure of Caryolan-1-ol Synthase, a Sesquiterpene Synthase Catalyzing an Initial Anti-Markovnikov Cyclization Reaction.

In a continuing effort to understand reaction mechanisms of terpene synthases catalyzing initial anti-Markovnikov cyclization reactions, we solved the X-ray crystal structure of (+)-caryolan-1-ol synthase (CS) from Streptomyces griseus, with and without an inactive analog of the farnesyl diphosphate (FPP) substrate, 2-fluorofarnesyl diphosphate (2FFPP), bound in the active site of the enzyme. The CS-2FFPP structure was solved to 2.65 Å resolution and showed the ligand in an elongated orientation, incapable of undergoing the initial cyclization event to form a C1-C11 bond. Intriguingly, the apo CS structure (2.2 Å) also had electron density in the active site, in this case, well fit by a curled-up tetraethylene glycol molecule recruited, presumably, from the crystallization medium. The density was also well fit by a molecule of farnesene suggesting that the structure may mimic an intermediate along the reaction coordinate. The curled-up conformation of tetraethylene glycol was accompanied by dramatic rotation of some active-site residues in comparison to the 2FFPP-structure. Most notably, W56 and F183 undergo 90° rotations between the 2FFPP complex and apoenzyme structures, suggesting that these residues provide interactions that help curl the tetraethylene glycol molecule in the active site, and by extension perhaps also a derivative of the FPP substrate in the normal course of the cyclization reaction. In support of this proposal, the CS W56L and F183A variants were observed to be severely restricted in their ability to catalyze C1-C11 cyclization of the FPP substrate and instead produced predominantly acyclic terpene products dominated by farnesol, β-farnesene, and nerolidol.

Evaluation of the reactivity of co-combustion of wheat straw and waste rubber thermolysis char

The co-combustion of wheat straw (WS) and waste rubber thermolysis char (WRTC) was examined with the perspective of utilizing WRTC as a high-calorific value fuel addition to agricultural biomass. The study investigated the effect of different proportions of WS-WRTC blends (10/15/25/49 wt% WRTC) and a maximum of 4 wt% binders, including potato starch and calcium oxide, on the reactivity of co-combustion and the distribution of products during the process. Thermogravimetric analysis with Fourier Transform Infrared Spectroscopy (TGA-FTIR) analyses was employed at a temperature range of 25–1000 °C with a heating rate of 10 °C/min. The kinetics of co-combustion were analyzed using the Fraser-Suzuki (FS) deconvolution method and a model-based kinetic modeling. The results indicate that a 10% addition of WRTC char reduces the intensity and rate of combustion and prolongs the combustion time. It was observed that the optimal addition to the blend is 25% WRCT, and it resulting in a reduction in activation energy and combustion indexes. However, it remains with no significant impact on process stability and efficiency. Kinetics of the decomposition of the WRTC25 mixture modeled by the deconvolution method indicates a 5-step reaction course, which is a combination of the characteristic combustion stages of both fuels. The main denoted functional group observed in the FTIR absorption spectra were C=O, C-O, O-H, and C-H related to the release of CO2, CO, H2O, CH4, aromatic compounds, and hydrocarbons.

ADAPTATION OF NAVAL PENTATHLON ATHLETES TO PHYSICAL TRAINING

Rationally planned training leads to adaptation and progress, and irrational planning leads to disruption of the course of adaptation reactions and overwork. For a rational periodization it is very important to identify training concepts based on detailed analysis of fatigue development mechanisms. Proper planning and execution of training will result in an increase in effort capacity. Adaptation, viewed from a biological point of view, is a complex defense mechanism against the demands caused by environmental changes. This requires an adequate response of the organism to environmental conditions in order to survive under the new conditions. For sports training, adaptation refers to the set of transformations that the athlete's body undergoes in training, in order to develop a superior state of bio-psycho-motor balance, materialized in the easy execution of a task. Research objectives: Initial evaluation of subjects; Development of the training program; Evaluation of the level of adaptation to physical effort obtained from specific naval pentathlon training; Development of a training planning model, allowing the improvement of physical effort capacity by means specific to the naval pentathlon. Methods: The research carried out started from the premise that the appropriate use of training means specific to the naval pentathlon can lead to an improvement of the effort capacity of military students, which fully satisfies their performance needs in fulfilling combat missions arising from the graduate's model. At a preliminary stage of the research, by applying general physical training tests, we obtained an initial assessment of the research subjects. These data were a benchmark in developing the training program and setting effort parameters. The training plan thus designed contains training sessions specific to naval pentathlon trials, adapted to the normal conditions of the naval academy training process. Results: The comparative analysis of the results, based on mathematical-statistical and graphical methods, reveals significant increases in performance recorded in the final testing stage. The dynamics of the results demonstrates a significant evolution of the results of the experimental group carried out during the training program, carried out according to the designed model. This confirms to us the effectiveness of applying the training program. The statistical results confirm a very good evolution of the results for the general motor tests and for the Ruffier test. Conclusions: Regular exercise is a particularly important stimulus for adaptation. Sports training, by its specific means, aims to increase the level of performance. In order to achieve this objective, it is necessary to apply a well-defined programme in great detail. Effective training requires constant variability in programming. In addition, in order to maximize the positive transfer of training, the means used in the training lesson should be as close as possible to the characteristics of the effort. Because of this, there is a permanent conflict in training programming, between diversity and specificity. This conflict can only be successfully managed through professional intervention on the part of the coach and involvement of the athlete according to training requirements.

Two targets, one strike: Efficient recovery of lithium and simultaneous removal of impurities from spent LFP batteries via ferric ions assisted air oxidation method

Recycling of spent lithium-ion batteries (LIBs) has become urgently imperative to address global environmental issues and achieve sustainable development of new energy industries. Prioritizing lithium and aluminum leaching is an ideal path for recovering lithium efficiently from spent LFP and preparing high-purity battery-grade FePO4. Here, a novel ferric ions-assisted air oxidation method was proposed for the simultaneous leaching of Li and Al. Fe3+ was ingeniously introduced playing two roles: acting as a catalyst for air oxidation and leaching aluminum. 98.8% Li and 95.2% Al are selectively leached under optimal conditions. The thermodynamic analysis indicated that the displacement reaction between Al and Fe3+ dominates the leaching of Al. Furthermore, Cl− can promote the leaching of Al by forming a stable complex [AlCl4]− with Al3+. The reaction course and mechanism were clarified by various characterizations, which indicate that the successful selective leaching of lithium does not destroy the original structure of LFP and the presence of carbon coatings. A cycling process was proposed for enriching the Li+ concentration and reusing Fe3+, and then Li2CO3 with a purity of 99wt.% was successfully prepared. This method demonstrates excellent economic efficiency and environmental friendliness, thus providing a sustainable and low-carbon recycling route for the spent LFP industry.

Large Molecular Rotation in Crystal Changes the Course of a Topochemical Diels-Alder Reaction from a Predicted Polymerization to an Unexpected Intramolecular Cyclization.

A designed anthracene-based monomer for topochemical Diels-Alder cycloaddition polymerization crystallized with head-to-tail arrangement of molecules, as revealed by single-crystal X-ray diffraction (SCXRD) analysis. The diene and dienophile units of adjacent monomer molecules are aligned at an average distance of 4.6 Å, suggesting a favorable crystalline arrangement for their intermolecular Diels-Alder cycloaddition reaction to form a linear polymer. Surprisingly, heating the monomer crystals at a temperature above 125 °C resulted in the formation of intramolecular Diels-Alder cycloadduct, which could be characterized by various spectroscopy and SCXRD analysis. Various time-dependent studies such as NMR, PXRD, and DSC, studies established that the reaction followed topochemical pathway. Schmidt's topochemical postulates are generally used to predict the topochemical reactivity and product, by analyzing the crystal structure of the reactant. Though the crystal arrangement predicted polymerization, upon heating, the molecule avoided this pathway by undergoing a large rotation to form an intramolecular cycloadduct. Theoretical calculations supported the feasibility of the rotation, exploiting the flexibility of the molecule and voids present. These findings caution that the reliance on Schmidt's criteria for topochemical reactions may sometimes be misleading, especially in heat-induced reactions.

Polymerization of six-membered propylene oxalate

Ring-opening polymerization (ROP) of the six-membered cyclic propylene oxalate was studied for the first time. The reaction proceeded with a high limiting conversion of about 96 % at 100 °C in the presence of tin(II) octoate. Linear macromolecules, Mw of 20–30 × 103, Ð ∼ 2, represented 86 % of the product, 4 % came from the equilibrium concentration of monomer, while the rest 10 % were cyclic oligomers consisting of 3–10 repeat units. ROP was accompanied by partial (about 30 %) conversion of the catalyst into the insoluble tin(II) oxalate in the course of polymer cross-linking reaction. The kinetics of polymerization obeyed first-order law, indicating typical for ROP constant number of active centers during the process. Polymerization without catalyst was 2000 times slower and also resulted in formation of polymer with Ð ∼ 2. Addition of benzyl alcohol to the polymerization mixture resulted in its inclusion into linear macromolecules and a decrease in their molecular weight. The results point to the possibility of synthesizing propylene oxalate block copolymers using macroinitiators with hydroxyl end groups.

Control Circuits for Potentiostatic/Galvanostatic Polarization and Simultaneous Chemical Sensing by a Light-Addressable Potentiometric Sensor.

A light-addressable potentiometric sensor (LAPS) is a semiconductor-based sensor platform for sensing and imaging of various chemical species. Being a potentiometric sensor, no faradaic current flows through its sensing surface, and no electrochemical reaction takes place in the course of LAPS measurement. In this study, a four-electrode system is proposed, in which a LAPS is combined with the conventional three-electrode electrochemical system. A LAPS is included as the fourth electrode for potentiometric sensing and imaging of the target analyte in the course of an electrochemical reaction taking place on the surface of the working electrode. The integrated system will be useful for analyzing dynamic processes, where both the electrochemical process on the electrode surface and the ion distribution in the solution need to be simultaneously investigated. Different grounding modes of control circuits that can simultaneously conduct potentiostatic/galvanostatic polarization and LAPS measurement are designed, and their functionalities are tested. The interference between polarization and LAPS measurement will also be discussed.

Hybrid Cellulosic Substrates Impregnated with Meta-PBI-Stabilized Carbon Nanotubes/Plant Extract-Synthesized Zinc Oxide-Antibacterial and Photocatalytic Dye Degradation Study.

Novel fibrous cellulosic substrates impregnated with meta-polybenzimidazole (PBI)-stabilized carbon nanotubes/zinc oxide with different weight content of ZnO and with the use of dimethylacetamide as dispersant media. The pristine ZnO nanoparticle powder was prepared by plant extract-mediated synthesis using Vaccinium vitis-idaea L. The green synthesized ZnO possesses an average crystallite size of 15 nm. The formation of agglomerates from ZnO NPs with size 250 nm-350 nm in the m-PBI@CNTs/ZnO was determined. The prepared materials were investigated by PXRD analysis, XPS, SEM, EDS, AFM, and TEM in order to establish the phase and surface composition, structure, and morphology of the hybrids. The potential of the synthesized hybrid composites to degrade methylene blue (MB) dye as a model contaminant in aqueous solutions under UV illumination was studied. The photocatalytic results show that in the course of the photocatalytic reaction, the m-PBI@CNTs/ZnO 1:3 photocatalyst leads to the highest degree of degradation of the methylene blue dye (67%) in comparison with the other two studied m-PBI@CNTs/ZnO 1:1 and 1:2 composites (48% and 41%). The antibacterial activity of ZnO nanoparticles and the hybrid CNT materials was evaluated by the RMDA and the dynamic contact method, respectively. The profound antibacterial effect of the m-PBI@CNTs/ZnO hybrids was monitored for 120 h of exposition in dark and UV illumination regimes. The photocatalytic property of ZnO nanoparticles significantly shortens the time for bactericidal action of the composites in both regimes. The m-PBI@CNTs/ZnO 1:2 combination achieved complete elimination of 5.105 CFU/mL E. coli cells after 10 min of UV irradiation.