Composition Of Reaction Mixture Research Articles

Commercial turpentine oil enriched with α-terpineol using an acid heterogeneous catalyst

The hydration of α-pinene, limonene, β-pinene, and commercial turpentine oil in the presence of strong acidic cation exchange resin Amberlyst-15 was studied. The acid catalytic hydration was performed in a batch reactor, and the effect of solvent at various temperatures and reaction times was evaluated. The main hydration product obtained from α-pinene was α-terpineol with a yield of 36 % (4 h, 70 °C, 2-propanol as solvent); however, the selected catalytic system was even more active to obtain α-terpineol when β-pinene was used as a substrate, obtaining α-terpineol yield of 38 % in 2 h of reaction. For the hydration of turpentine (70 °C, turpentine:water:2-propanol mass ratio of 1:0.5:2, 15 % w/w catalyst) the composition of reaction mixture after 4 h was 35 % w/w of α-terpineol, 8 % w/w of α-pinene, and 0.5 % w/w of β –pinene, which correspond to a final content of α-terpineol similar to the concentration obtained when α-pinene was used as a substrate (36 % w/w).

Enzymatic synthesis of prebiotic galactooligosaccharides from galactose derived from gum arabic.

A novel enzymatic process was established for galactooligosaccharides (GOS) synthesis by using plant-derived galactose as substrate, without producing any byproducts. The galactose was prepared from the acid hydrolysate of gum arabic. The yeast Kluyveromyces lactis producing β-galactosidase capable of catalyzing GOS synthesis from galactose was screened out. The synthesis conditions using the yeast cells as enzyme source were optimized by both single-factor experiment and response surface methodology, with the highest GOS yield reached 45%. The composition of reaction mixture contained only GOS and unreacted galactose, which could be easily separated by the cation exchange resin column. The structures of major GOS products were identified as Gal-β-D-(1→6)-Gal, Gal-β-D-(1→3)-Gal, and Gal-β-D-(1→6)-Gal-β-D-(1→6)-Gal by MS and NMR spectra. Moreover, the β-galactosidase-containing cells can be recycled for at least 30 batches of GOS synthesis at 35°C, with the enzyme activity remaining above 60%.

Resins with Oxygen-Containing Functional Groups Obtained from Products of Fossil Fuels Processing: A Review of Achievements

To synthesize resins with oxygen-containing functional groups the C9 fractions of hydrocarbon pyrolysis, heavy gasoline, and light coal tar fraction obtained from coal coking liquid products (CCLP) were used. Various types of initiators and industrial monomers were obtained using the above-mentioned non-target and/or by-products of organic raw materials processing: by the initiated oligomerization method (from C9 fractions) – petroleum polymer resins with functional groups; by radical cooligomerization (from CCLP) (with RPKV) – coumarone-indene resins with functional groups. The influence of the main factors controlling the synthesis process of resins with functional groups on their quantitative and qualitative characteristics was studied, including the process temperature, duration, and the reaction mixture composition. The structure of the synthesized resins was analyzed by IR spectroscopy, and the presence of epoxy, carboxyl, hydroxyl, and methacrylate functional groups was confirmed.

Oxygen Tolerance during Surface-Initiated Photo-ATRP: Tips and Tricks for Making Brushes under Environmental Conditions.

Achieving tolerance toward oxygen during surface-initiated reversible deactivation radical polymerization (SI-RDRP) holds the potential to translate the fabrication of polymer brush-coatings into upscalable and technologically relevant processes for functionalizing materials. While focusing on surface-initiated photoinduced atom transfer radical polymerization (SI-photoATRP), we demonstrate that a judicious tuning of the composition of reaction mixtures and the adjustment of the polymerization setup enable to maximize the compatibility of this grafting technique toward environmental conditions. Typically, the presence of O2 in the polymerization medium limits the attainable thickness of polymer brushes and causes the occurrence of "edge effects", i.e., areas at the substrates' edges where continuous oxygen diffusion from the surrounding environment inhibits brush growth. However, the concentrations of the Cu-based catalyst and "free" alkyl halide initiator in solution emerge as key parameters to achieve a more efficient consumption of oxygen and yield uniform and thick brushes, even for polymerization mixtures that are more exposed to air. Precise variation of reaction conditions thus allows us to identify those variables that become determinants for making the synthesis of brushes more tolerant toward oxygen, and consequently more practical and upscalable.

Catalytic Performances of Co/TiO2 Catalysts in the Oxidative Dehydrogenation of Ethane to Ethylene: Effect of CoTiO3 and Co2TiO4 Phase Formation

Co/TiO2 catalysts with different cobalt loadings (3.8, 7.5 and 15 wt%) were prepared by impregnation method of Co(NO3)2 6H2O over titania. Samples containing Co(NO3)2·6H2O and TiO2 in stoichiometric proportions in order to obtain CoTiO3 and Co2 TiO4 phases were also synthesized. The effect of the calcination treatment at two different temperatures, 550 and 1150 °C, was investigated. Characterizations by several techniques, such as XRD, UV–vis–NIR, DRS, Raman and XPS, were carried out. XRD showed the coexistence of three phases: CoTiO3; Co2TiO4 and Co3O4 after calcination at 550 °C, while calcination at high temperature (1150 °C) led to single-phase systems (CoTiO3 or Co2TiO4). Diffuse reflection and XPS spectroscopy showed that divalent cobalt occupies octahedral sites in the ilmenite phase, and both tetrahedral and octahedral sites in the spinel phase. The catalytic performances of the prepared catalysts were evaluated in the oxidative dehydrogenation reaction (ODH) of ethane to ethylene, as a function of the Co content for Co/TiO2 catalysts and as a function of the calcination temperatures for the CoTiO3 and Co2TiO4 phases. Co(7.5)/TiO2 was the most active, although the conversion of ethane decreased in the first 150 min of the reaction, reaching values comparable to those of Co2TiO4 and CoTiO3; however, Co(7.5)/TiO2 was confirmed as having the best selectivity to ethylene in comparison with the bulk phases, CoTiO3 and Co2TiO4. The influence of the reaction mixture composition, specifically the presence of water, at different percentages, was investigated. There is a decrease in the overall ethane conversion and an increase in the ethylene selectivity when the percentage of water increases. This behavior can likely be attributed to an increase in the surface concentration of hydroxyl species (OH), resulting in heightened surface acidity.

Physicochemical, structural, and adsorption characteristics of DMSPS-co-DVB nanopolymers.

The aim of this work is the synthesis and characterization of the series of S,S'-thiodi-4,1-phenylene bis(thio-methacrylate)-co-divinylbenzene (DMSPS-co-DVB) nanomaterials. The series of new nanopolymers including three mixed systems with different ratios of DMSPS and DVB components, DMSPS-co-DVB = 1:1, DMSPS-co-DVB = 1:2, and DMSPS-co-DVB = 1:3, was synthesized in the polymerization reaction. The research task is to investigate the influence of the reaction mixture composition on morphological, textural, and structural properties of final nanosystems including size, shape, and agglomeration effect. The advanced biphasic nanomaterials enriched with thiol groups were successfully synthesized as potential sorbents for binding organic substances, heavy metals, or biomolecules. To determine the impact of the DMSPS monomer on the final properties of DMSPS-co-DVB nanocomposites, several techniques were applied to reveal the nano-dimensional structure (SAXS), texture (low-temperature nitrogen sorption), general morphology (SEM), acid-base properties (potentiometric titration), and surface chemistry and phase bonding effectiveness (FTIR/ATR spectroscopy). Finally, kinetic studies of aniline sorption on polymeric materials were performed.

Nano and mesosized selenium and its synthesis using the ascorbic acid route

Elemental selenium particles have undergone extensive research in recent years. They are interesting for their catalytic, antimicrobial, and many other properties which make them potentially useful in various applications. Despite the widespread research, there are still some information blank spots in the preparation of these nano- and mesosized objects by using a simple reduction reaction between sodium selenite and ascorbic acid without any stabilizing agents which could unpleasantly affect their natural characteristics. This work aimed to prepare these particles and characterize them in the dependence on the reaction mixture composition and pH. Firstly, the reaction system was monitored, in detail, by UV–VIS spectroscopy and a possible deviation in the detection of individual spectral peaks was detected. Furthermore, it is observable that the reaction becomes faster when lowering pH of the reaction mixture. The prepared particles were well-purified and characterized by X-ray powder diffraction, scanning electron, and transmission electron microscopy, where their morphology was observed. The size distribution of the particles was measured by dynamic light scattering and was ranging between 65 and 159 nm. Finally, the dependence of the sample forms on storage time was monitored. It has been shown that the individual objects maintain their primary structure and form, when stored in water, on contrary, dried particles undertook a significant structure and color-change, while forming crystalline polymorphs of gray selenium.

Rapid and Effective Way to Synthesize Highly Crystalline Nanosized SAPO-34 Particles.

SAPO-34 nanocrystals with sizes of 50-150 nm were obtained via steam-assisted crystallization (SAC) for 5 h at 200 °C from two types of aluminum precursors-aluminum isopropoxide and boehmite. A reaction mixture composition with a small amount of organic template tetraehylammonium hydroxide (TEAOH) was used with the molar ratio TEAOH/Al2O3 = 1/1. The alumina precursor type and duration of the SAC (5 and 24 h) on the crystal size, texture, and acid properties were investigated. The SAPO-34 nanocrystals that we obtained possess a large micropore volume of 0.22-0.24 cm3/g and a specific surface area of 651-695 m2/g. When the crystallization was prolonged for up to 24 h, a SAPO-18 structure appeared, but the micropore and mesopore volumes changed insignificantly. Using boehmite as the aluminum precursor led to higher mesoporosity of the material but a little bit lower acidity when compared with the samples prepared from aluminum isopropoxide. In addition, the method proposed was used for preparing a SAPO-34-coated aluminum adsorber heat exchanger. Thus, the synthesis method proposed is affordable and effective to prepare SAPO-34 highly crystalline nanoparticles, with no need for post-synthetic procedures as the mother liquor separation from nanocrystals.

Effect of the Composition of Reaction Mixture on Characteristics of Compact Titanium Diboride-Containing Materials Obtained by Self-Propagating High-Temperature Synthesis

Effect of the Composition of Reaction Mixture on Characteristics of Compact Titanium Diboride-Containing Materials Obtained by Self-Propagating High-Temperature Synthesis

Formation of geopolymeric materials properties depending on the molar modules of SiO2/Al2O3 and SiO2/Na2O

The construction sector is responsible for around 37% of global emissions of the carbon dioxide to the atmosphere. Therefore, reducing gas emissions, in this construction sector, is particularly important ,given the progressing climate change. For this reason, limiting its emissions and limiting the emission of other greenhouse gases in this sector, is of particular importance in view of the progress of climate change. It is important that new construction products have less impact on the environment during their entire life cycle, and their production has been decoupled from the use of primary energy. In this work, selected properties of geopolymeric materials were examined. Geopolymers are inorganic aluminosilicate polymers with an amorphous microstructure, which may be an alternative in certain applications, for products based on Portland cement. Here, the properties of geopolymer mortars, i.e. porosity, microstructure and mechanical strength, were compared. The influence of the composition of reaction mixture on these properties, defined by the appropriate SiO2/Al2O3 and SiO2/Na2O molar ratios, was also defined. The results show that increasing the content of SiO2 in relation to Al2O3 in the composition of the reaction mixture, reduces porosity. Thus, leading to a more compact microstructure and higher mechanical strength. A similar effect occurs when a higher NaOH solution concentration is used, in comparison to the sodium silicate [Na2SiO3] solution.

Deposition of Gadolinia-Doped Zirconia Layers Using Metalorganic Compounds at Low Temperatures.

This paper shows the results of an investigation on the synthesis of non-porous and nanocrystalline ZrO2-Gd2O3 layers by metalorganic chemical vapor deposition (MOCVD) with the use of Zr(tmhd)4 (tetrakis(2,2,6,6-tetramethyl-3,5-heptanedionato)zirconium(IV)) and Gd(tmhd)3 (tris(2,2,6,6-tetramethyl-3,5-heptanedionato)gadolinium(III)). Argon and air were used as carrier gases. The molar content of Gd(tmhd)3 in the gas reaction mixture was as follows: 10% and 20%. The layers were synthesized on tubular substrates made of quartz glass at the temperatures of 550–700 °C. Synthesis conditions were established using the Grx/Rex2 expression (Gr is the Grashof number; Re is the Reynolds number; x is the distance from the gas inflow point). The value of this criterion was below 0.01. ZrO2-Gd2O3 layers synthesized at 600–700 °C were crystalline. When the molar content of Gd(tmhd)3 in the gas reaction mixture was 10 mol.%, a relationship between the chemical composition of the gas reaction mixture and that of the deposited layer could be observed. The synthesized layers underwent scanning electron microscopy, as well as X-ray analysis. The transparency of coated and uncoated glass was tested using UV–Vis spectroscopy. Their chemical composition was examined with the use of an EDS analyzer.

ASSESSMENT AND APPLICATION OF MOLECULAR MARKERS IN BREEDING FOR THE RESISTANCE OF TOMATO (SOLANUM LYCOPERSICUM L.) TO LATE BLIGHT (PHYTOPHTHORA INFESTANS)

In order to use marker-assisted selection (MAS) methods in the development of hybrids and tomato varieties resistant to late blight, the efficiency of molecular markers to the alleles resistant to Phytophthora infestans known in the literature was assessed. High efficiency in the identification of homozygous and heterozygous forms using CAPS dTG63 (Hinf1) and SCAR NCLB-9-6678 markers to Ph2 and Ph3 alleles was established respectively. DNA extraction techniques, reaction mixture compositions, as well as amplification and visualization result modes were adapted. The
 presence of the Ph3 allele in F1-standard Adapt and Alamina hybrids, and F1 Azart, Agenchik, Dzivosny, and Black Brilliant hybrids included in the Register of Varieties of the Republic of Belarus, as well as in the breeding lines of the collections possessed by the Institute of Genetics and Cytology, NAS of Belarus, and the Belarusian State Agricultural Academy was demonstrated.

FEATURES OF IN SITU FORMATION OF MIXTURES OF LINEAR POLYMERS

This article is devoted to the analysis of the results of the investigation of the process of forming mixtures of linear polymers formed simultaneously in situ according to different mechanisms. The first mechanism is polyaddition, the second mechanism is radical polymerization. This is one of the possible ways to obtain multicomponent polymer systems. The kinetics of chemical reactions of the formation of components and the phase separation which accompanies these reactions were studied for mixtures of poly(methyl methacrylate) (PMMA) with two polyurethanes (PU) of different chemical nature of both flexible and rigid blocks. PU-1 was synthesized from macrodiisocyanate based on oligo(tetramethylene glycol) with molecular mass 1000 g·mol–1 and hexamethylene diisocyanate taken in the molar ratio 1 : 2 using diethylene glycol as a chain extender. PU-2 was synthesized from macrodiisocyanate based on olygo(propylene glycol) with molecular mass 1000 g·mol–1 and toluylene diisocyanate taken in the molar ratio 1 : 2 using butanediol as a chain extender. The mixture of polystyrene (PS) with PU-2 was studied too. It is established that regardless of the chemical nature of the components, the process of in situ mixture formation is subject to general laws. In particular, the change in the chemical nature of the component formed by the mechanism of polyaddition (mixtures PMMA/PU-1 and PMMA/PU-2) or of the component formed by radical polymerization (mixtures PMMA/PU-2 and PS/PU-2) does not affect the nature of the dependence of the conversion degree of components and the fraction of formed polymers at the beginning of the phase separation on the composition of the initial reaction mixtures. Only the absolute values of these parameters change due to different reactivity and different thermodynamic compatibility of the mixed components.

Comparative Performance of PETase as a Function of Reaction Conditions, Substrate Properties, and Product Accumulation.

There is keen interest to develop new technologies to recycle the plastic poly(ethylene terephthalate) (PET). To this end, the use of PET-hydrolyzing enzymes has shown promise for PET deconstruction to its monomers, terephthalate (TPA) and ethylene glycol (EG). Here, the Ideonella sakaiensis PETase wild-type enzyme was compared to a previously reported improved variant (W159H/S238F). The thermostability of each enzyme was compared and a 1.45 Å resolution structure of the mutant was described, highlighting changes in the substrate binding cleft compared to the wild-type enzyme. Subsequently, the performance of the wild-type and variant enzyme was compared as a function of temperature, substrate morphology, and reaction mixture composition. These studies showed that reaction temperature had the strongest influence on performance between the two enzymes. It was also shown that both enzymes achieved higher levels of PET conversion for substrates with moderate crystallinity relative to amorphous substrates. Finally, the impact of product accumulation on reaction progress was assessed for the hydrolysis of both PET and bis(2-hydroxyethyl) terephthalate (BHET). Each enzyme displayed different inhibition profiles to mono(2-hydroxyethyl) terephthalate (MHET) and TPA, while both were sensitive to inhibition by EG. Overall, this study highlights the importance of reaction conditions, substrate selection, and product accumulation for catalytic performance of PET-hydrolyzing enzymes, which have implications for enzyme screening in the development of enzyme-based polyester recycling.

Analysis of the Morphology and Structure of Carbon Deposit Formed on the Surface of Ni3Al Foils as a Result of Thermocatalytic Decomposition of Ethanol.

This article presents the results of investigations of the morphology and structure of carbon deposit formed as a result of ethanol decomposition at 500 °C, 600 °C, and 700 °C without water vapour and with water vapour (0.35 and 1.1% by volume). scanning electron microscopy (SEM) and scanning transmission electron microscopy (STEM) observations as well as energy dispersive X-ray spectrometry (EDS), X-ray diffraction (XRD), and Raman spectroscopic analyses allowed for a comprehensive characterization of the morphology and structure of cylindrical carbon nanostructures present on the surface of the Ni3Al catalyst. Depending on the reaction mixture composition (i.e., water vapour content) and decomposition temperature, various carbon nanotubes/carbon nanofibres (CNTs/CNFs) were observed: multiwalled carbon nanotubes, herringbone-type multiwall carbon nanotubes, cylindrical carbon nanofibers, platelet carbon nanofibers, and helical carbon nanotubes/nanofibres. The discussed carbon nanostructures exhibited nickel nanoparticles at the ends and in the middle part of the carbon nanostructures as catalytically active centres for efficient ethanol decomposition.

Novel modes of synchronization in star networks of coupled chemical oscillators.

Photochemically coupled micro-oscillators are studied experimentally and computationally in star networks to investigate the modes and mechanisms of synchronization. The micro-oscillators are catalyst-loaded beads that are placed in catalyst-free Belousov-Zhabotinsky (BZ) solutions. The properties of the photochemical coupling between the oscillators are determined by the composition of the BZ reaction mixtures, and both excitatory coupling and inhibitory coupling are studied. Synchronization of peripheral oscillators coupled through a hub oscillator is exhibited at coupling strengths leading to novel modes of synchronization of the hub with the peripheral oscillators. A theoretical analysis provides insights into the mechanism of the synchronization. The heterogeneous peripheral oscillators have different phase velocities that give rise to a phase divergence; however, the perturbation from the hub acts to realign the phases by delaying the faster oscillators more than the slower oscillators.

POWER RATE LAW BASED CHEMICAL KINETICS AND THERMODYNAMIC MODELING OF AFRICAN PEAR SEED OIL CONSECUTIVE IRREVERSIBLE BASE METHANOLYSIS FOR BIODIESEL PRODUCTION

Currently the major challenge of biodiesel application as a replacement to petrodiesel is its industrial production sustainability.Consequently, the successful scale-up of laboratory results in transesterification requires so much information obtained through chemical kinetics.This paper presents the kinetics and thermodynamic study of alkali-homogeneous irreversible methanolysis of seed oil derived from African pear. The transesterification process was carried out from 0-100 minutes at temperature range of 55-65°C. The reaction mixture compositions were ascertained using gas chromatography- flame ionization detector (GC-FID) technique. Rate constants of the triglyceride (Tg), diglycerides (Dg) and monoglycerides(Mg) hydrolysis were in the range of 0.0140- 0.07810 wt%/min and increased with increase in temperature. The rate of reaction was found to increase with increase in temperature. Activation energies were found to be 6.14, 20.01 and 28.5kcal/mol at 55, 60 and 65oC respectively. Tg hydrolysis to Dg was observed asthe rate determining step while the reaction agreed with second order principles. A biodiesel yield of 93.02% was obtained with cloud point of 10°C , flash point of 125°C , pour point of 4°C , calorific value of 34.4MJ/kg, and cetane number of 54.90 which satisfy EN14214 and ASTM D 6751 standards. Results presented in this report would serve as idealized conditions for industrial scale up of biodiesel production from African pear seed oil. Keywords:Kinetics; methanolysis; rate constants; activation energy; African pear seed oil; biodiesel

Development and Testing of a Method for Detecting Lujo Virus RNA by Reverse Transcription and Real Time Polymerase Chain Reaction

The aim of the study was to develop and assess the efficacy of a method for Lujo virus RNA detection in clinical and biological samples using one-step real-time RT-PCR.Materials and methods. In order to select the conservative regions of the genome, we utilized the available in GenBank database Lujo virus sequences (https://www.ncbi. nlm.nih.gov/genbank) aligned in BioEdit 7.2.5 software package ( (IbisBiosciences, USA). To conduct one-round RTPCR, reverse transcriptase and TaqF-polimerase were used. Recombinant Escherichia coli strain, XL1-Blue, containing pGEM-T plasmid with inserted synthetically-generated fragment of the virus genome, was produced to make positive control sample (PCS). Constructed recombinant plasmids were used for creating RNA-containing PCS with protective protein shell of MS2-phage. Determination of specificity of the developed method was performed with the help of control panel of RNA and DNA of 23 viral strains related to 10 families; the sensitivity – the panel of biological samples artificially contaminated with PCS. Further testing was carried out at the premises of laboratory of the Russian-Guinean Center for Epidemiology and Prevention of Infectious Diseases (Kindia, Republic of Guinea) on 265 blood sera from practically healthy persons, 110 blood sera of cattle, 83 suspensions of ticks, and 165 suspensions of organs of small mammals collected in the territory of Guinea.Results and discussion. Two conservative polymerase gene fragments have been chosen as targets for Lujo virus RNA detection using RT-PCR. The combination of primers and probes has been experimentally selected, optimum composition of reaction mixture for PCR and mode of RT-PCR set-up established, as well as control samples C+, internal control, positive control sample developed. Sensitivity of the proposed method is 5·103 GE /ml, specificity – 100 %.

Study on the Synthesis of Chabazite Zeolites via Interzeolite Conversion of Faujasites.

The interzeolite conversion of faujasite (FAU-type) zeolites to chabazite (CHA-type) zeolite in the presence of N,N,N-trimethyladamantammonium and N,N,N-dimethylethylcyclohexylammonium cations was investigated over a large compositional range by carefully controlling the reaction mixture compositions. Highly crystalline CHA zeolites were also obtained by the transformation of several zeolite types including EMT, LTL, LEV, RTH, and MFI frameworks. The formation of CHA zeolite from FAU zeolite precursors was substantially faster than that from zeolite L with a similar composition. High-silica CHA zeolites were also produced successfully using a mixture of TMAda with a number of less expensive organic structure-directing agents. The CHA zeolite materials have been synthesized with high crystallinity and with a Si/Al ratio ranging from 5 to 140. Our data support the importance of structural similarity between the zeolite precursors, nucleation/crystallization processes, and the zeolite product in the interzeolite conversion compared to conventional amorphous aluminosilicate gels. Our synthetic methods could be used to prepare other 8-membered ring zeolites such as AEI and AFX frameworks, potential candidates for selective catalytic reduction of NOx, light olefin production, and CO2 abatement.

Studies on Preparation, Characterization and Application of Porous Functionalized Glycidyl Methacrylate-Based Microspheres.

A one-step swelling and polymerization technique was used in the synthesis of porous glycidyl methacrylate (GMA) and ethylene glycol dimethacrylate (EGDMA) monodisperse polymeric microspheres. The polystyrene (PS) seed obtained in the dispersion polymerization was used as a shape template. The presence of epoxide rings in the chemical structure of microspheres enables their post-polymerization chemical modifications involving: the Diels-Alder reaction with sodium cyclopentadienide and maleic anhydride, the reaction with 4,4′-(bismaleimido)diphenylmethane, and the thiol-Michael reaction with methacryloyl chloride and 2-mercaptopropionic acid. Changing the reaction mixture composition—the amounts of crosslinking monomer and PS seed as well as the type and concentration of porogen porous microspheres of different porous structures were obtained. Their porous structures were characterized in the dry and swollen states. The copolymers obtained from the equimolar monomers mixture modified in the above way were applied as the column packing materials and tested in the reverse-phase HPLC (High-Performance Liquid Chromatography). A few factors influencing morphology and porous structure of microspheres were studied.