Blank Test Research Articles

Pitfalls in Photochemical and Photoelectrochemical Reduction of CO2 to Energy Products.

The photochemical and photoelectrochemical reduction of CO2 is a promising approach for converting carbon dioxide into valuable chemicals (materials) and fuels. A key issue is ensuring the accuracy of experimental results in CO2 reduction reactions (CO2RRs) because of potential sources of false positives. This paper reports the results of investigations on various factors that may contribute to erroneous attribution of reduced-carbon species, including degradation of carbon species contained in photocatalysts, residual contaminants from synthetic procedures, laboratory glassware, environmental exposure, and the operator. The importance of rigorous experimental protocols, including the use of labeled 13CO2 and blank tests, to identify true CO2 reduction products (CO2RPs) accurately is highlighted. Our experimental data (eventually complemented with or compared to literature data) underline the possible sources of errors and, whenever possible, quantify the false positives with respect to the effective conversion of CO2 in clean conditions. This paper clarifies that the incidence of false positives is higher in the preliminary phase of photo-material development when CO2RPs are in the range of a few 10s of μg gcat-1 h-1, reducing its importance when significant conversions of CO2 are performed reaching 10s of mol gcat-1 h-1. This paper suggests procedures for improving the reliability and reproducibility of CO2RR experiments, thus validating such technologies.

Amine-coated nanobubbles-assisted flotation of fine and coarse quartz

This study investigates the role of alkyl ether monoamine-coated nanobubbles (NBs) in assisting the flotation process of quartz across various particle sizes, on a bench scale. Experiments were conducted in a mini lab column utilizing a consortium of bubble sizes: D32 = 1200 μm for macrobubbles and D32 = 180–220 nm for amine-coated NBs. The study revealed that an increase in amine-coated NBs correlates well with a decrease in the air/solution’s interfacial tension caused by the ether amine at less than 68 mN m−1. True flotation recoveries with varying amine/g quartz, where the collector-frother amine may be amine-coated NBs alone or assisted by NBs generated in pure water, were compared with blank tests, in the absence of NBs. The flotation study evaluated size-to-size fractions from fine (−20 µm) to coarse (up to 150 µm) particles and their mixtures. In addition, the work extended to explore the behavior of the “super” coarse quartz from 150 µm up to 1000 µm. The results highlighted a clear dependence on the particle size, with NBs improving recoveries in all fractions, especially the difficult-to-treat ultrafine/fine and coarse quartz. Recovery results exceeded 90 % in all fractions (isolated or in mixtures) at a high rate with the amine-coated NBs. The mechanisms proposed improved flotation performance attributed to the high numerical concentrations of NBs (at least 2–3 × 1010 NBs per gram of quartz) rapidly attaching to quartz surfaces, serving as “seeds” for the adhesion of larger bubbles generated in conventional flotation cells. This interaction facilitates the formation of lightweight, cluster-like aggregates that swiftly rise to the column’s surface. Notably, larger quartz particles (+355 µm) form the bigger hydrophobic and buoyant clusters, leading to their rapid levitation and effective phase separation, with over 95 % separation efficiency. This innovative technique’s significance, outcomes, and potential scalability are thoroughly discussed, highlighting its promising applicability in diverse mineral and ore flotation systems, particularly those containing quartz and silicates.

Primary alcohol-induced coacervation in alkyl polyglucoside micellar solution for supramolecular solvent-based microextraction and chromatographic determination of phthalates in baby food

This study reports for the first time the phenomenon of supramolecular solvent formation based on alkyl polyglucoside as an amphiphile and primary alcohol as a coacervation agent. The physical properties (density, kinematic viscosity, phase diagram for ternary system) of the supramolecular solvent were investigated, and a mechanism for its formation was proposed. A green and simple microextraction procedure for preconcentration and determination of phthalates in baby foods packaged in plastic packaging was developed as proof-of-concept example. The microextraction procedure assumed separation of analytes from solid phase sample in micellar solution of decyl glucoside and in situ formation of supramolecular solvent for analytes preconcentration after addition of n-heptanol. The determination of phthalates in obtained extracts was implemented by high-performance liquid chromatography with UV–Vis detection. The limits of detection, calculated from a blank test based on 3σ, were determined to be 10 μg kg−1 for dimethyl phthalate, diethyl phthalate, di-n-butyl phthalate, and di-n-octyl phthalate. The developed procedure did not require filtration of sample suspension, and assumed the use of green and biodegradable substances for the supramolecular solvent formation across a wide pH range.

Enhancing CO2 desorption efficiency with Non-Aqueous Catalyst-Enhanced Tri-Blend amines

The substantial energy demand of CO2-loaded solvent regeneration constitutes a significant economic challenge for the industrial applications of CO2 capture and utilization technologies. The nano-catalysts have the capability to improve CO2 desorption while reducing the energy demands for solvent regeneration. This study focuses on examining the absorption–desorption performance of non-aqueous tri-blend amines (monoethanolamine (MEA), methyl diethanol amine (MDEA), and piperazine (PZ)) utilizing different amounts of catalysts including HZSM-5, H-ferrierite (FER), and H-mordenite (MOR), γ-aluminium-oxide (Al2O3), titanium-oxide (TiO2), magnesium oxide (MgO), indium-oxide (In2O3). The incorporation of solid catalysts leads to a substantial enhancement in the desorption performance of tri-blend amines and reduced energy consumption in comparison to blank tests. Higher desorption efficiency occurred with the presence of lower catalyst amounts. The sequence of CO2 desorption heat duty performance reduction with 0.125 g catalyst, was as follows: MgO (70.9 %) > In2O3 (80.2 %) > HZSM-5 (84.1 %) > Al2O3 (84.2 %) > FER (87.1 %) > MOR (88.4 %) > TiO2 (89.7 %), relative to blank test (100 %). HZSM-5 exhibited the highest desorption factor as 4.25*10-7 mol3/kJmin while increasing the desorption rate to 2.37*10-3 mol/min. This study provides the desorption performance of non-aqueous amine blends with energy-efficient catalysts, highlighting their potential as promising materials for carbon capture and storage applications with improved energy efficiency.

CORROSION INHIBITION BEHAVIOUR OF CUSTARD APPLE LEAVES AND ACACIA CONCINNA EXTRACT ON MILD STEEL IN ACIDIC MEDIA: ADSORPTION AND THERMODYNAMIC STUDY

Custard apple leaves extract (CALE) was tested to evaluate corrosion inhibition efficiency for mild steel under acidic medium. The test metal substrate was collected over a period of 24 hr of contacting with acid to determine the corrosion inhibition efficiency (CIE) and corrosion rate (CR) using the Gravimetric analysis. The findings of the study were applied to examine the adsorption behavior and thermodynamic characteristics for CALE as a potential corrosion inhibitor in acidic environment. Mild steel exhibited the highest corrosion rate in the absence of a corrosion inhibitor in a 0.5 M sulphuric acid solution. However, the rate of corrosion was observed to decrease gradually with increase in CALE concentration (0.4–2.0 g/l). The similar trend was noted at the experimental temperature range of 298-328 K. Adsorption behavior was investigated using the Langmuir, Temkin, Freundlich, and Flory Huggins adsorption isotherm models. The Temkin adsorption isotherm model provides the best fit to the experimental data. Besides, the negative values of Gibb’s free energy of adsorption (ΔGad) reveal strong evidence for the spontaneous nature of CALE adsorption on mild steel surface. The increase in activation energy (Ea) from 35.05 kJ/mol in the blank test solution to 68.03 kJ/mol at 2.0 g/l concentration of CALE indicates the formation of a protective film of inhibitor molecules on the metal surface. Adsorption enthalpy values (∆H=31.28-73.79 kJ/mol) over the concentration range (0-2.0g/l of CALE) implies physical adsorption, whereas negative entropy values (ΔS) suggests free movement of inhibitor molecules in the bulk solution. Additionally, a synergistic effect was demonstrated in lowering the corrosion rate by combining Acacia concinna extract (ACE, 0.1-0.3 g/l) with CALE, thereby enhancing the overall corrosion inhibition efficiency. For citation: Jitendra Kisan Shinde, Ravindra Gulab Puri, Pawan Devidas Meshram, Rajkumar Shankarrao Sirsam Corrosion inhibition behaviour of Custard apple leaves and Acacia concinna extract on mild steel in acidic media: adsorption and thermodynamic study. ChemChemTech [Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol.]. 2024. V. 67. N 7. P. 119-126. DOI: 10.6060/ivkkt.20246707.7038.

Liquid-phase microextraction approach using supramolecular solvent formed in aqueous systems based on di(2-ethylhexyl)phosphoric acid salt: Spectrophotometric determination of antipyrine in saliva

In this study, di(2-ethylhexyl)phosphoric acid salt was investigated as a double-chain anionic surfactant for supramolecular solvent formation in a liquid-phase microextraction procedure for the first time. Inorganic electrolytes (sodium salts) were shown to be coacervation agents, due to their salting-out property in solution of sodium di(2-ethylhexyl)phosphate, obtained by deprotonation of the acid. The physico-chemical properties of the newly synthesised solvents were studied. Sodium carbonate and sodium phosphate were found to be the most suitable coacervation agents, due to their alkaline nature and low viscosity of the supramolecular solvent phases they produce. The extraction ability of the novel solvent was demonstrated in liquid-phase microextraction of a colored derivative of antipyrine from saliva for further spectrophotometric determination. The extraction recovery was found to be 70 %. The proposed green sample preparation technique enabled the exclusion of traditional toxic solvents and reduction of reagent consumption. The satisfactory analytical performance of the procedure was validated with real sample analysis. The calibration graph was linear over the concentration range of 0.03 to 0.5 mmol/L. The limit of detection (3σ) and limit of quantification (10σ), calculated from blank tests, were 0.01 and 0.03 mmol/L, respectively.

Hydrogen Formation from Water with Various Reducing Metals Catalyzed by In Situ-Generated Nickel Nanoparticles

Water is a potential green source for the generation of clean elemental hydrogen without contaminants. One of the most convenient methods for hydrogen generation is based on the oxidation of different metals by water. The inspection of the catalytic activity toward hydrogen formation from water performed in this study was carried out using four different metals, namely, zinc, magnesium, iron, and manganese. The process is catalyzed by in situ-generated nickel nanoparticles. The zinc–water system was found to be the most effective and exhibited 94% conversion in 4 h. The solid phase in the latter system was characterized by PXRD and SEM techniques. Several blank tests provided a fundamental understanding of the role of each constituent within the system, and a molecular mechanism for the catalytic cycle was proposed.

Screening of 152 Veterinary Drug Residues in Animal Source Foods by LC-MS/MS, Multilaboratory Validation Study: Final Action 2020.04.

The presence of veterinary drug residues in food-producing animals and animal products is regulated through the enforcement of maximum residue limits (MRLs). To answer the need of the food sector to monitor these substances in a wide range of food commodities, stakeholders at AOAC INTERNATIONAL identified the need for a reliable confirmatory screening method. Such a qualitative approach is required for compliance checking and to support product release in manufacturing. Data were collected from five independent laboratories that applied the First Action Official Method 2020.04 to demonstrate adequate performance under reproducibility conditions. The probability of detection (POD) was calculated in blank test samples and test samples spiked at the screening target concentration (STC) level, with the objective to achieve PODs ≤10% and ≥90%, respectively. Additionally, the effectiveness of the screening method was evaluated by participating in 92 proficiency tests. Four streams were optimized to screen for 152 veterinary drug residues by LC-MS/MS in a wide variety of food commodities including milk-based ingredients and related products (e.g., milk fractions, infant formula, infant cereals, and baby foods), meat- and fish-based ingredients and related products (fresh, powdered, cooked, infant cereals, and baby foods), and other ingredients based on eggs, animal fat, and animal byproducts. The four streams covered 105 antibiotic residues, anti-inflammatory and antiparasitic agents (stream A), 23 beta-lactams (stream B), 14 aminoglycosides (stream C), and 10 tetracyclines (Stream D). The multilaboratory validation led to PODs at the STC ≥94% and PODs in the blank ≤9%. Further application of the multilaboratory validated method to 92 proficiency tests provided more than 99% satisfactory submitted results (n = 784). The interlaboratory reproducibility determined for this method met the acceptance criteria defined in AOAC Standard Method Performance Requirement (SMPR®) 2018.010. AOAC has approved the method for Final Action status.

High Purity Solvents for qNMR Measurement

Quantitative NMR (qNMR) has been adopted by documentary standards, including the Japanese Pharmacopoeia (JP), United States Pharmacopoeia (USP), and International Organization for Standardization (ISO), owing to its reliability and efficiency. Note that qNMR can be used for quantifying target components using the signal integration ratio of an analyte to a reference. In qNMR, a modern NMR instrument with high resolution and sensitivity is used to record reliable spectra. This instrument can detect small signals from impurities in a solvent, which may result in inaccurate signal integration in the spectrum. In this study, we investigated the influence of solvent quality on qNMR accuracy focusing on organic impurities, water content, and deuteration ratio. If signals from organic impurities and signals from the analyte overlap, the duplication of signal integration will directly affect the qNMR analytical result. To examine overlapping, we performed blank solvent tests. Additionally, a high water content and low deuteration ratio affect the detection sensitivity, thus reducing the signal-to-noise (S/N) ratio of the target. Thus, these factors must be considered to obtain accurate qNMR results.

Catalytic Pyrolysis of Naomaohu Coal Using Combined CaO and Ni/Olivine Catalysts for Simultaneously Improving the Tar and Gas Quality

Catalytic pyrolysis of low-rank coal is currently an effective method for producing high-quality tar and gas. In this study, catalytic upgrading of volatiles from Naomaohu (NMH) coal pyrolysis has been conducted in a two-stage fixed-bed reactor using combined CaO and Ni/olivine (Ni-loaded olivine) catalysts. The effect of catalyst distribution modes and catalytic temperature on the tar and gas quality has been investigated. Simulated distillation and GC-MS analysis have been used to investigate the distribution of tar components. The results indicated that the light oil fraction in tar dramatically increased due to the combination of CaO and Ni/olivine. The CaO-Ni/olivine mode is especially better compared to the layouts of the Ni/olivine-CaO mode and the mixed mode. The CaO-Ni/olivine mode ensures a higher light fraction in tar at 69.3% and a light oil fraction at 29.8% at a catalytic temperature of 450 °C, while the heavy tar fraction decreased to 30.7%. Meanwhile, the contents of benzene (heteroatomic substituents) in tar significantly increased from 2.55% to 6.45% compared with the blank test. In this scenario, CaO breaks down macromolecular compounds in tar and cleaves long-chain esters to produce aliphatic hydrocarbons. These hydrocarbons are then dehydrogenated to produce lighter aromatic hydrocarbons over the CaO surface. Subsequently, the volatiles pass through the Ni/olivine catalysis, where ether compounds are produced by means of dehydration reactions. In addition, the CaO absorbs the CO2 in the pyrolysis gas, leading to an elevation of CH4 and H2 concentration. Particularly, the concentration of H2 significantly increased from 16.2% to 30.37%, while the concentration of CO2 significantly decreased from 37.9% to 10.57%. These findings suggest that the usage of combined CaO and Ni/olivine catalysts is beneficial for improving both the tar and gas quality.

Development of a Bioaerosol Sampling Method for Airborne Pathogen Detection with Focus on SARS-CoV-2

As worldwide evidence shows that the predominant transmission route of SARS-CoV-2 and other respiratory pathogens is airborne, the need for suitable methods for the sampling of bioparticles directly from the air is more urgent than ever. The present paper describes the development of a method for the collection of biological aerosols, using a preexisting cyclonic impinger, the Coriolis μ, combined with a lysis buffer and subsequent qPCR analysis of the generated samples in lab. Four phases of method development are described: exploratory, validation, blank tests, and application. The application phase consisted of a field experiment in which the method was simultaneously applied at two daycare facilities. The method achieved a good level of accuracy and reliability in detecting different types of infectious agents in the air, with a global uncertainty of 19.6%. Furthermore, our method allows the simultaneous detection of 26 different respiratory pathogens in air samples, it is relatively simple, and the equipment is easy to use. Additionally, the time to collect a representative sample is short compared to other methods. The method does not cause significant disturbance to those present in the sampled rooms, and it is safe for operators and flexible, meaning it can be used in virtually any environment regardless of use, size, or occupancy. Further research is being developed to allow quantitative analysis of the collected samples and to test the methods’ ability to assess the viability of the microorganisms collected in the sample.

CO2 Photoreduction Product Selectivity with TiO2−Cu Nanocatalysts under Different Reaction Media

AbstractThis study explores photocatalytic conversion of CO2 using TiO2−Cu heterojunctions with different Cu contents and investigates influence of different reaction media on the process efficiency. The use of KOH favored liquid products, especially ethanol. An analysis of H2 production as the main competitive reaction was done. Sodium oxalate led to an increase in H2 evolution by approximately 600 μmol g‐1 compared to pure water, in the presence of CO2 in the reaction medium, but the blank test (without CO2) indicates a lower H2 yield (~136 μmol g−1), which suggests that the competitive reaction with CO2 also plays a role in H2 production. This role was related to the decrease of the initial pH from approximately 8.5 to 5.2, stabilizing at 5.5 at the end of the 6 h reaction. In an environment saturated with N2, the pH increases to 9 and stabilizes at 7.8 at the end of the process. In the presence of acetic acid, both CO and H2 production were suppressed, with a significant increase in the selectivity for methane via cleavage of the acid‘s carbon bond. The findings underscore the importance of optimizing reaction conditions to achieve higher yields of desired products in the photocatalytic conversion of CO2.

Effect of strain rate on the stress corrosion cracking of TP439 stainless steel in water vapor environment at 500 ℃

The effect of water vapor on the stress corrosion cracking (SCC) behavior of TP439 stainless steel at 500 °C was investigated using slow strain rate tensile tests at three strain rates of 2 × 10–5/s, 2 × 10–6/s, and 2 × 10–7/s. Air was selected as a comparative blank test environment for the water vapor environment. The results showed that the tensile strength of the specimens increased significantly in air when the strain rate was decreased from 2 × 10–5/s to 2 × 10–7/s, while it decreased in water vapor. Dynamic strain aging (DSA) and SCC are the main factors contributing to the difference in tensile strength of the specimens in air and water vapor. The SCC of TP439 stainless steel in water vapor at 500 °C occurs at a strain rate of 2 × 10–7/s or even lower. Based on the SCC susceptibility index and SEM observation of specimen fracture, TP439 stainless steel exhibits a slight transgranular SCC in water vapor with low SCC susceptibility.

Experimental study and analysis of the effect of detergent on the production of biogas from toilet drainage system linked to biogas digester in Ethiopia

A biogas reactor that is coupled to a Toilet drainage system collects, stores, and treats excreta through the anaerobic digestion process. According to the data collected, cleaning agents directly get into the drainage system in most households. In this experimental study, the effect of detergent on the production of biogas from a toilet-connected reactor was analyzed. Three predominantly used household cleaning agents with anionic and ionic surfactants were considered and sample mixtures were prepared for 1:1:1 ratio. The experiment has been carried out in a 5-liter plastic bottle as a biogas reactor. The relationships between generated gas and its chemical compositions at various detergent concentrations (blank test, 80 ppm, 160 ppm, 320 ppm 400 ppm 800 ppm, and 1200 ppm) have been investigated using a Gas Chromatography Mass Spectrometry (GCMS) system and analyzed. The risk of Hydrogen sulfide production on human health has also been assessed at different Concentrations of Detergent (CoDe). The results demonstrate that during the early phases (blank test to 80 ppm) of CoDe addition, methane production increases from 62.5% to 63.8% but subsequently decreases by 6% as CoDe increases from 160 ppm to 320 ppm followed by adrastic reduction subsequently. This results in a reduction of methane production by 23% and a higher formation of gases like N2, HCl, NaC12H25SO4, C20H37NaO7S, and others. Therefore, the addition of cleaning agents above 320 ppm into a biogas reactor not only causes substandard biogas production but also has a risk to human health and the environment as a result of the higher production of hydrogen sulfide.

Numerical modeling for shearing of unidirectional carbon fiber reinforced plastic laminates by means of near-net-shape blanking

Structural components made of carbon fiber reinforced plastics (CFRP) exhibit a high degree of lightweight suitability. In order to fulfill geometric and functional requirements, a finishing process step of outer and inner contours is necessary. Near-net-shape blanking processes show potential for economical finishing of CFRP structural components. For the knowledge-based design of a near-net-shape blanking process comparable to fine blanking an understanding of the separation mechanisms during shearing of CFRP laminates is required. Therefore, this paper deals with the development of a finite element (FE) process model for near-net-shape blanking of unidirectional (UD) CFRP laminates with different fiber volume fraction and fiber orientation. Material modeling of the UD CFRP laminates was carried out by means of experimental characterization based on tensile, compression and shear tests. The formulation of the material model was implemented using a VUMAT user subroutine. The application of the blank holder and counter force was realized using a kinematic model based on a VUAMP user subroutine. A validation based on experimental near-net-shape blanking tests will be conducted in the next step.

Thermomechanical modeling of the shearing process during fine blanking of quenched and tempered steel

In order to develop an alloy design for fine blanking of deformation mechanism-based sheet metal materials such as high manganese steel, knowledge of the temperature during the shearing process is required. Thermomechanical modeling of shear zone temperature requires consideration of contact heat transfer, which depends on stress state as well as temperature. This paper deals with a methodology for calibrating the contact heat transfer coefficient during fine blanking using indirect temperature measurements. For this purpose, a thermomechanically coupled finite element (FE) model was designed considering thermoviscoplasticity, temperature-dependent physical and thermophysical parameters as well as a steady-state calibrated contact heat transfer coefficient. Experimental fine blanking tests were carried out to validate the model using force, die roll and thermography measurements based on varied blanking velocities. The thermomechanically coupled FE modeling showed a sufficiently accurate correspondence regarding the experimentally determined blanking force, die roll as well as sheared surface temperature. Thermographically determined sheared surface temperatures allowed calibration of locally different contact heat transfer coefficients as a simplified approach under steady-state conditions.

Structure optimization of heterogeneous compound eye camera for improving the detection performance

To achieve fast location, precise tracking and accurate identification over a large field of view (FOV), we have proposed a heterogeneous compound eye camera (HeCECam), which consists of a heterogeneous compound eye array, an optical relay system and a CMOS detector. However, the current HeCECam can hardly acquire high-precision 3D information of the targets to realize these applications. To solve this challenge, we propose a scheme on optimizing the structure of the HeCECam to improving the detection performance, including the optimization of the distribution uniformity of the sub-eyes with the proposed “Three-direction center-of-gravity subdivision (TGS)” and the enhancement of the compatibility between heterogeneous compound eyes and the optical relay system with the proposed compensation method for tilt. The TGS significantly reduces the distribution unevenness of sub-eyes down to 117% from the previous 152%, and provides symmetry to the heterogeneous compound eye array. The tilt compensation effectively addresses previous imaging defects, such as distortion of sub-images, increased stray light, and support structures being imaged, and it improves the imaging clarity of the system, especially in external FOV. Based on two proposed methods, we re-design and fabricate the heterogeneous compound eye array to obtain a high-performance prototype. To verify the imaging capacities of the optimized HeCECam, a series of comparison experiments are performed, including blank scene imaging, FOV tests, resolution verification and real-world scene imaging. The results show that the previous imaging defects have been well eliminated, and the optimized prototype has stronger resolving power and wider FOV. This allow the HeCECam to perform better in subsequent practical applications, such as wide-area surveillance, forewarning, and navigation.

Evaluating the Potential of Biodegradable Carbohydrates and the Aqueous Extract of Potato Pulp to Inhibit Calcium Carbonate Scale in Petroleum Production

Summary Scale is a significant operational concern in petroleum production that is commonly addressed by using chemical inhibitors. However, commercial inhibitors can potentially be pollutants depending on their composition and method of disposal. Consequently, evaluating the potential of biodegradable molecules to inhibit scale has gained attention. This study evaluates the effect of a series of carbohydrates (i.e., glucose, fructose, sucrose, maltose, maltodextrin, and soluble starch) and the aqueous extract of potato pulp on calcium carbonate precipitation and scale formation. Precipitation tests were conducted by combining aqueous solutions of sodium bicarbonate (3000 mg L−1) and calcium chloride (4000 mg L−1) in the presence of each carbohydrate, the aqueous extract of potato pulp, or a commercial inhibitor (1000 mg L−1). The precipitation was monitored through RGB (red, green, and blue) image analysis and pH measurements. The induction time in the presence of glucose, fructose, maltose, and sucrose is two to three times longer than in the blank test (in the absence of an inhibitor). This effect is slightly more pronounced in the presence of maltodextrin and soluble starch (approximately four times longer). However, the drop in pH and the mass of solids recovered is similar for all the carbohydrates tested (~0.5 mg and 120 mg, respectively), suggesting that carbohydrates slightly influence the precipitation kinetics but do not affect the precipitation equilibrium. Scanning electron microscopy (SEM) and X-ray powder diffraction (XRD) analysis reveals that calcium carbonate precipitates as calcite and vaterite in the blank test. In the presence of glucose, fructose, maltose, and maltodextrin, calcium carbonate exclusively precipitates as calcite. However, in the presence of sucrose and soluble starch, calcium carbonate precipitates as both calcite and vaterite. Interestingly, a more prominent amount of vaterite was observed in the presence of soluble starch. All carbohydrates decrease the crystallite size of calcite, while sucrose and soluble starch increase the crystallite size of vaterite. The crystalline phases were also identified by Raman spectroscopy, ruling out the presence of any amorphous calcium carbonate phase. The inhibitory effect of soluble starch and the aqueous extract of potato pulp on calcium carbonate scale formation was evaluated in a dynamic scale loop (DSL) system. Soluble starch slightly delays scale formation even at high concentrations (1000 mg L−1). Conversely, the aqueous extract of potato pulp demonstrates enhanced performance by delaying scale formation by approximately 20 minutes for a 1-psi increase in the pressure of the tube and by more than 40 minutes for a 4-psi increase. As a result, it exhibited an impact on the kinetics of solid deposition. This agrees with the precipitation test in the presence of the potato extract (PE), which increases the induction time (from 2 minutes to 32 minutes), decreases the mass of solids (from 116 mg to 35 mg), and forms more distorted and smaller particles of calcite. These findings suggest a promising approach for the development of green scale inhibitors utilizing aqueous extracts of starchy foods or even starchy foods waste water.

Analysis of combustion characteristics of wood stack and absolute ethanol in fire extinguishing experiment

For the purpose of researching the rules of combustion heat release, ammonium phosphate dry powder extinguishing agent and water-based fire extinguishing agent were utilized before and after the class A fire common wood stack ignition fuel and class B fire anhydrous ethanol ignition fuel fire extinguishing. For wood stack fire, 0.5A wood stack was used for blank combustion test, and the pan fire ignition method for the same type and scale of wood stack fire extinguishing experiment. For absolute ethanol fire, fire suppression was studied using a 13B scale. The change characteristics of the combustion field before and after action of the dry powder extinguishing agent and water system extinguishing agent were measured by thermocouple, heat flow meter and digital camera. The findings of the experiment demonstrated that in the combustion experiment of wood stack, the temperature of 0.5A wood stack of the blank group could reach 800 °C, and the temperature reduction rate of free combustion was 2.62 °C/s. It took an average of 36.5s and 2.25 kg of ammonium phosphate dry powder to put out the fire，and the temperature reduction rate was 4.18 °C/s. The average amount of water-based extinguishing agent used to extinguish a fire was 1.21 kg, yet the average time to do so was just 12.5 s, and the average rate of temperature drop was 10.14 °C/s. In the experiment where an ethanol pool fire was being burned, the typical amount of water-based fire extinguishing chemical used was 3.44 kg, and the typical extinguishing time was 18 s, the maximum temperature drop rate could reach 35.6 °C/s in the initial stage of fire extinguishing, despite the fact that the dry powder fire extinguisher containing ammonium phosphate was used, the fire was not properly controlled.

A Green Approach to Obtaining Glycerol Carbonate by Urea Glycerolysis Using Carbon-Supported Metal Oxide Catalysts.

The results of sustainable and selective synthesis of glycerol carbonate (GC) from urea and glycerol under ambient pressure using carbon-fiber-supported metal oxide catalysts are reported. Carbon fibers (CF) were prepared via a catalytic chemical vapor deposition method (CCVD) using Ni as a catalyst and liquefied petroleum gas (LPG) as a cheap carbon source. Supported metal oxide catalysts were obtained by an incipient wetness impregnation technique using Zn, Ba, Cr, and Mg nitrates. Finally, the samples were pyrolyzed and oxidized in an air flow. The obtained catalysts (10%MexOy/CFox) were tested in the reaction of urea glycerolysis at 140 °C for 6 h under atmospheric pressure, using an equimolar ratio of reagents and an inert gas flow for NH3 removal. Under the applied conditions, all of the prepared catalysts increased the glycerol conversion and glycerol carbonate yield compared to the blank test, and the best catalytic performance was shown by the CFox-supported ZnO and MgO systems. Screening of the reaction conditions was carried out by applying ZnO/CFox as a catalyst and considering the effect of reaction temperature, molar ratio of reagents, and the mode of the inert gas flow through the reactor on the catalytic process. Finally, a maximum yield of GC of about 40%, together with a selectivity to glycerol carbonate of ~100%, was obtained within 6 h of reaction at 140 °C using a glycerol-to-urea molar ratio of 1:1 while flowing Ar through the reaction mixture. Furthermore, a positive heterogeneous catalytic effect of the CFox support on the process was noticed.