Addition Of Alkali Research Articles

Photo-responsive Pickering emulsions triggered by in-situ pH modulation using a photoacid generator

HypothesisPickering emulsions that respond to changes in pH by the addition of acid or alkali have been extensively studied, but the development of photo-responsive Pickering emulsions has been more challenging. This study attempts to demonstrate a novel approach to achieve photo-responsiveness in Pickering emulsions by incorporating a photoacid generator (PAG) into the oil phase. Upon UV irradiation, the PAG is expected to release protons (H+), which can then regulate the pH of the emulsion system and control its stability. ExperimentsAmphiphilic colloidal particles obtained by modifying silica particles with poly (2-(dimethylamino)ethyl methacrylate) (SiO2-PDMAEMA) are used to stabilize the Pickering emulsions. The protonation and deprotonation of the SiO2-PDMAEMA particles at different pH values allow for the tuning of emulsion stability. By introducing the PAG into the stable Pickering emulsion system and applying UV irradiation to trigger the in-situ release of H+, the pH of the emulsion is systematically decreased, and the corresponding changes in emulsion stability are investigated. FindingsThe results show that UV irradiation alone cannot induce emulsion instability. However, when PAG is added to the oil phase, the Pickering emulsions exhibit a significant decrease in pH under UV irradiation, ultimately leading to emulsion destabilization and phase separation. At a UV intensity of 20 mW/cm2 for 2 min, the H+ release from the PAG significantly lower the emulsion’s pH, causing the SiO2-PDMAEMA particles to detach from the oil–water interface and resulting in emulsion instability. Higher concentrations of SiO2-PDMAEMA particles in the emulsion require more PAG to induce instability, as confirm by confocal laser scanning microscopy (CLSM) image. This study presents a versatile approach to develop photo-responsive Pickering emulsions which can have potential applications in areas such as drug delivery, cosmetics, and responsive materials.

Sulfide and Fe-Ti-P liquid immiscibility in the Ni-Cu-Co ovoid deposit of the Voisey’s Bay complex, Labrador, Canada

AbstractIn the Voisey’s Bay complex, sulfide-matrix breccias developed through the percolation of dense sulfide melt, leading to the displacement of the silicate melt within partially molten silicate-matrix breccias. In these sulfide matrix-breccias, hydrous silicate rims are commonly present at the interface between the sulfide matrix and the silicate framework. Multiple lines of evidence support a magmatic origin of these hornblende-biotite rims, which was largely coeval with the emplacement of the sulfide melt in the magmatic breccias. The formation of the hornblende-biotite rims required the addition of alkalis and water that could not have entirely been sourced from either the sulfide melt or the silicate framework. Through the integration of compositional maps with major and trace element analyses of the main accessory minerals, we propose that the critical components required for the development of the hydrous silicate rims in sulfide-matrix breccias originated from an immiscible Fe-Ti-P melt. Distinct textural and compositional features of apatite, hercynite, ilmenite and magnetite support the presence of small amounts of Fe-Ti-P melt in the sulfide melt. This Fe-Ti-P melt likely formed through melt immiscibility in the early stages of the development of the Voisey’s Bay complex, and was transported in the magma conduits together with the sulfide melt.

Effect of salt and alkali on the viscoelastic behavior of noodle dough sheet with different wheat starch granule sizes

The underlying mechanisms of salt and alkali on the viscoelastic behaviors of noodle dough sheets with varied B/A-type starch ratios were investigated from water state, protein polymerization and conformation, and microstructure. The viscoelastic behaviors of dough sheets increased with increasing B/A-type starch ratio, regardless of the presence of salt and alkali, indicating the addition of salt and alkali did not change the effect law of starch granule size on dough viscoelasticity. The viscoelastic moduli of dough decreased in the presence of salt and alkali, and the effect was more obvious as the ratio of B/A-type starch decreased, which was mainly determined by the interactions of protein-protein, protein-starch, and starch-starch in dough systems. In the low ratio of B/A-type starch dough sheets, NaCl enhanced the non-covalent interactions and β-sheet structure, while alkali promoted the covalent cross-linking of protein. In the high ratio B/A-type starch dough samples, the big starch surface area provided by a high phase volume of starch granules led to the domination of starch-starch interactions over the protein phase, thus determining the viscoelastic behavior of dough. SEM images showed that NaCl caused the gluten to form a fibrous structure, while alkali induced a membrane-like and more closed structure. NaCl and alkali showed different influences on water distribution, molecular conformation, and network structure of dough sheets with varied B/A-type starch ratios and thus contributed to the different viscoelastic behaviors.

Multifunctional polymeric stationary phases with enhanced hydrophilicity grafted with polyethyleneimine and polyglycidol

Two methods for increasing the degree of hydrophilization and screening of the sorbent matrix based on a copolymer of styrene and divinylbenzene grafted with polyethyleneimine quaternized with glycidol are proposed. The first method involves the polymerization of glycidol in the functional layer by varying the pH of the reaction medium, and the second method involves modifying the matrix by oxidizing the double bonds on its surface to obtain anchor epoxy groups. It was demonstrated that in the first method, the optimal approach is the twofold addition of glycidol before and after the addition of alkali, as in this case, the first addition of glycidol is consumed for the quaternization of polyamine, and the second for polymerization in ion-exchange centers. The new method of matrix modification, combined with the developed method of creating hydrophilic layers, significantly reduced the retention of oxyhalides, haloacetic acids, and polarizable anions in ion chromatography with suppressed background conductivity and amino acids in hydrophilic chromatography up to the point of changing the elution order. The obtained stationary phases are suitable for the simultaneous determination of standard inorganic anions, oxyhalides, and anions of haloacetic or alkylphosphonic acids in ion chromatography, as well as for the separation of amino acids, sugars, and vitamins in hydrophilic chromatography.

Impact of Nano-SiO2 on the Compressive Strength of Geopolymer-Solidified Expansive Soil

Expansive soil is widely distributed and often needs to be improved for engineering and construction needs. Using blast furnace slag and fly ash as precursors and NaOH as an alkali activator, a geopolymer was prepared to solidify expansive soil, and the effect of nano-SiO2 on the compressive strength and water stability of the geopolymer-solidified expansive soil was further studied. The effects of alkali addition ratio, nano-SiO2 addition ratio, and curing agent addition ratio on the unconfined compressive strength and water stability of the cured soil were studied through unconfined compressive strength tests, and the curing mechanism was analyzed by electron microscopy scanning. The experimental results showed that the unconfined compressive strength and water stability of geopolymer-stabilized soil first increased and then decreased with an increase in alkali activator dosage. The optimal dosage of alkali activator was found to be 12.5%. Furthermore, it was found that adding nano-SiO2 can further enhance the strength and water stability of solidified soil. When the content of nano-SiO2 was 3%, the unconfined compressive strength was increased by 15%. With an increase in the content of nano-SiO2 doped polymer (GFNS), the unconfined compressive strength and water stability of the solidified soil showed a trend of first increasing and then decreasing, reaching a peak at a content of 20%. The cementitious materials, such as hydrated calcium silicate and hydrated calcium silicate aluminate, generated by the reaction between nano-SiO2 and geopolymer played a role in bonding and filling in the solidified soil. Under the joint action of the two, the structural arrangement between the solidified soil particles became more compact, which improved the strength of the solidified soil.

Impact of curing conditions on the mechanical properties and micro characteristics of alkali-activated material synthesized from industrial waste soda residue

Alkali-activated materials (AAM) are considered a type of green cementitious material because they are produced without the grinding and calcining required for cement production, significantly reducing carbon emissions. However, their production typically involves the use of commercial alkalis, which are often corrosive, irritating, and expensive. As an industrial waste from sodium carbonate production, soda residue (SR) has a large reserve and is challenging to dewater and utilize, making its disposal a widespread technical challenge. In this paper, considering the alkaline nature and high salt content of SR, a soda residue activated granulated blast-furnace slag cementitious material (SAG) was synthesized directly using undried and unground SR slurry as the alkali activator, with a mass ratio of SR to granulated blast-furnace slag (GBFS) of 30:70. The effects of ambient temperature (AT) curing, water curing, various heat curing temperatures (45°C, 60°C, 75°C, and 90°C), and different heat curing durations (6 h, 12 h, 18 h, and 24 h) on the properties of SAG were investigated. Specifically, the effect of curing conditions on the mechanical properties of SAG was analyzed through unconfined compressive strength (UCS) testing of mortar specimens. The impact of curing conditions on the phase composition and changes in SAG was characterized using XRD, TG, and FTIR, while the effect on the microstructure of SAG was characterized using SEM. The results showed that SAG achieved the highest UCS (3 d/56 d: 28.1 MPa/36.7 MPa) when subjected to heat curing at 75°C for 12 h. The UCS increased significantly by 3022 % and 321 %, respectively, compared to those under AT sealed curing. This was attributed to the fact that SAG under heat curing produced more C-(A)-S-H gels and hydrocalumite crystals, optimizing pore structure and resulting in a denser microstructure. However, exceeding the threshold temperature of 75°C led to an excessively rapid hydration reaction that adversely affected the further dissolution of GBFS and the uniform distribution of hydration products, thereby diminishing the positive effects of heat curing on UCS. In addition, excessively prolonging the heat curing time exacerbated the development of microcracks within the SAG, leading to a deterioration of UCS over age. In this paper, a novel AAM was synthesized using undried and unground industrial waste without the addition of commercial alkali, and the impact of curing conditions on their properties was studied. This broadens the range of applications for SAG, fills a gap in research on the impact of curing conditions on AAM without commercial alkali, and provides a theoretical basis for the low-carbon utilization of industrial waste.

Continuous production of pure formic acid solution from CO2 hydrogenation at room temperature via amine-functionalized PdMn nano-alloy

CO2 hydrogenation into formic acid is of great significance to mitigate CO2 emission. However, conventional routes typically require the addition of unrecyclable bases to shift the reaction equilibrium by the formation of formate, which leads to complex subsequent separation and difficulty in continuous production of pure formic acid solution. Here we report a secondary amine-modified PdMn nanocatalyst for the continuous production of pure formic acid solution in fixed-bed reactors via CO2 hydrogenation. By optimizing fine structure of PdMn nano-alloy, the optimal TOF of up to 26.5 h−1 is obtained under mild reaction conditions (25 ℃, 3.0 MPa). This is one of the highest levels reported for a heterogeneous catalyst without alkali additives under similar conditions. The characterization shows that the two-component alloying effect of PdMn and the synergistic effect between PdMn NPs and secondary amine group (NH) are the key to obtaining superior reactivity. These findings in this work may pave an avenue for conversion of CO2 in a more environmentally friendly way.

Impact of exposure conditions on alkali-silica reaction in alkali-activated material systems

The influence of different testing methods on alkali-silica reaction (ASR) behavior is a result of the difference in the effect of exposure conditions on it. This study investigated the impact of temperature and the addition of alkali on ASR behavior in an alkali-activated material (AAM) system and compared it with an ordinary Portland cement (OPC) system. The results showed that the ASR in the AAM system was more independent of the exposure conditions than that in the OPC system because of its inherently high alkalinity and dense microstructure. More ASR products with higher Na:Si ratios were evident in the alkali-activated slag (AAS) mortars than in the OPC mortars. The accelerated test conditions developed for OPC systems could be applied to AAM systems. However, owing to the difference in the acceleration effect, comparing the ASR-induced expansion in OPC and AAM systems using the accelerated test method was misleading to some extent. This study contributes to the understanding of the ASR in AAM systems and is of considerable importance for the industrial application of AAMs.

Accelerated carbonation of non-plastic soils mixed with hydrated lime: index properties influencing binder formation rate and mechanical improvement

Chemical stabilization—the mixing of additives like cement, lime, or fly-ash with soil to improve its mechanical properties—conventionally relies on hydration reactions to generate a binder. Accelerated soil carbonation is a nascent alternative method, whereby carbon dioxide is intentionally introduced in soil mixed with alkali additives to generate a carbonate binder and sequester carbon dioxide. Non-plastic sand and silt specimens mixed with hydrated lime were carbonated for varying amounts of time at different water contents and densities to evaluate the index properties influencing the rate of carbonation and degree of mechanical improvement. It was demonstrated that volumetric air and water contents primarily govern the rate of binder formation and that mechanical properties are influenced by the carbonate binder content and density. Under optimum conditions, soil specimens could be fully carbonated within 3 to 24 hours and unconfined compressive strengths as great as 3 to 4 MPa were achieved. The degree of strength improvement is comparable to cement-stabilized materials with similar dependence on soil type, density, and binder content. If techniques are developed that enable carbonation at scale, the sequestration of carbon dioxide would offset emissions associated with production of chemical additives used for chemical stabilization.

Electrochemical Recovery of N and P from Municipal Wastewater

Phosphorus, P, is a vital element of paramount importance for both humans and for the Environment. Wastewater contains often relatively high concentrations of P which can be recovered as crystalline struvite (MgNH4PO4·6H2O, MAP). This option is quite attractive in assisting sustainable development because struvite can be used as a slow-release fertilizer. Domestic wastewater is usually high in P and nitrogen, N, but relatively poor in magnesium, Mg. It is necessary to develop low-cost solutions for the enrichment of wastewater with Mg. In the present work, sacrificial magnesium anodes were used, which dissolve upon anodic polarization, releasing sufficient magnesium for the selective precipitation of MAP. The application of constant current between two electrodes of which the anode is a low-cost magnesium cylindrical rod (4 cm2 exposed surface area) and the other a platinum cathode electrode, both immersed in ammonium phosphate solutions, without adjustment of the solution pH, was investigated. Constant current density over the range 10–100 A·m−2, between the Mg- Pt electrodes immersed in solutions of ammonium hydrogen phosphate of exactly known initial concentration, was applied using a potentiostat. In the presence of sodium chloride solutions, on the magnesium anode and in the bulk solution, Mg(OH)2 (brucite) formed because of the passivation of the Mg electrode. In dilute ammonium hydrogen phosphate solutions, the magnesium anode dissolution resulted in struvite precipitation, even at a low applied current (10 mA). Struvite crystals with an average size of 20 μm were precipitated. The behavior of the cell for the electrolyte solutions used was Faradaic as long as the surface coverage of the anode was relatively low. The anodic dissolution of Mg resulted in high pH values (pH 11) eliminating the need for alkali addition.

Accelerated surface carbonation of non-plastic silt mixed with hydrated lime

Chemical stabilization via hydration reactions with cement or lime is a universally applied method to improve the mechanical properties of shallow soils. Accelerated soil carbonation is a nascent approach intended to bypass this reaction. Carbon dioxide gas is deliberately introduced at high concentrations to react with the alkali additives and precipitate a carbonate binder that permanently sequesters carbon dioxide in the process. A large soil box experiment was performed to examine the efficacy of an accelerated surface carbonation approach, which has the potential to be applied over large areas. High concentrations of carbon dioxide gas were introduced at grade beneath a seal to facilitate vertical penetration into lime-mixed silt. The real-time progression of accelerated soil carbonation was captured with a gas flowmeter and a distributed array of embedded thermocouples and bender elements for the first time. Post-carbonation measurements of binder content and California Bearing Ratio (CBR) verified the degree of carbonation and associated mechanical improvement. Synthesis of real-time monitoring data and post-carbonation measurements indicate carbonation progressed top-down 150 to 200 mm below grade within 5 h, resulting in a substantial increase in strength and stiffness. Potential challenges and benefits associated with adoption of accelerated surface carbonation are discussed.

CO2 Fixation to Prebiotic Intermediates over Heterogeneous Catalysts.

ConspectusThe study of the origin of life requires a multifaceted approach to understanding where and how life arose on Earth. One of the most compelling hypotheses is the chemosynthetic origin of life at hydrothermal vents, as this condition has been considered viable for early forms of life. The continuous production of H2 and heat by serpentinization generates reductive conditions at hydrothermal vents, in which CO2 can be used to build large biomolecules. Although this involves surface catalysis and an autocatalytic process, in which solid minerals act as catalysts in the conversion of CO2 to metabolically important organic molecules, the systematic investigation of heterogeneous catalysis to comprehend prebiotic chemistry at hydrothermal vents has not been undertaken.In this Account, we discuss geochemical CO2 fixation to metabolic intermediates by synthetic minerals at hydrothermal vents from the perspective of heterogeneous catalysis. Ni and Fe are the most abundant transition metals at hydrothermal vents and occur in the active site of the enzymes carbon monoxide dehydrogenases/acetyl coenzyme A synthases (CODH/ACS). Synthetic free-standing NiFe alloy nanoparticles can convert CO2 to acetyl coenzyme A pathway intermediates such as formate, acetate, and pyruvate. The same alloy can further convert pyruvate to citramalate, which is essential in the biological citramalate pathway. Thermal treatment of Ni3Fe nanoparticles under NH3, which can occur in hydrothermal vents, results in Ni3FeN/Ni3Fe heterostructures. This catalyst has been demonstrated to produce prebiotic formamide and acetamide from CO2 and H2O using Ni3FeN/Ni3Fe as both substrate and catalyst. In the process of serpentinization, Co can be reduced in the vicinity of olivine, a Mg-Fe silicate mineral. This produces CoFe and CoFe2 with serpentine in nature, representing SiO2-supported CoFe alloys. In mimicking these natural minerals, synthetic SiO2-supported CoFe alloys demonstrate the same liquid products as NiFe alloys, namely, formate, acetate, and pyruvate under mild hydrothermal vent conditions. In contrast to the NiFe system, hydrocarbons up to C6 were detected in the gas phase, which is also present in hydrothermal vents. The addition of alkali and alkaline-earth metals to the catalysts results in enhanced formate concentration, playing a promotional role in CO2 reduction. Finally, Co was loaded onto ordered mesoporous SiO2 after modification with cations to simulate the minerals found in hydrothermal vents. These catalysts were then investigated under diminished H2O concentration, revealing the conversion of CO2 to CO, CH4, methanol, and acetate. Notably, the selectivity to metabolically relevant methanol was enhanced in the presence of cations that could generate and stabilize the methoxy intermediate. Calculation using the machine learning approach revealed the possibility of predicting the selectivity of CO2 fixation when modifying mesoporous SiO2 supports with heterocations. Our research demonstrates that minerals at hydrothermal vents can convert CO2 into metabolites under a variety of prebiotic conditions, potentially paving the way for modern biological CO2 fixation processes.

High-performance biodegradable poly(vinyl alcohol)/starch composites via alkaline-regulated crystalline engineering

The increasing demand for environmentally-friendly products has led to a growing focus on the development of high-performance biodegradable materials. However, achieving a balance between mechanical strength, water resistance, and biodegradability remains a challenge. Herein, the successful preparation of exceptional biodegradable poly(vinyl alcohol) (PVA)/starch (ST) composites using alkaline-regulated crystalline engineering is reported. The findings demonstrate that the alkali promotes ST gelatinization while inhibiting its recrystallization, resulting in improved compatibility and good dispersion in the PVA matrix. In contrast, the alkali enhances the crystallization of PVA, thereby improving the composites' water resistance. The composites exhibit outstanding mechanical properties, with a strain at break of approximately 400 % and a toughness of 54 MJ/m3, surpassing most reported works. Even in high humidity and water environments, the composites maintain their mechanical strength, with a strength of 13 MPa after soaking in water for 1 d, significantly higher than films without the addition of alkali. Moreover, the composites exhibit excellent biodegradability, with a degradation rate exceeding 40 % after a 60-d natural soil burial test. The flame retardancy is also greatly enhanced, with a limiting oxygen index (LOI) of 30 %. This study offers a promising avenue for the development of high-performance biodegradable materials such as dip-coating fabric, fire retardant coating, and industrial packaging.

Experimental investigation and thermomechanical performance evaluation of supercritical water oxidation of n‐dodecane/tributyl phosphate

AbstractBACKGROUNDNuclear energy has brought immense benefits while also generating a large amount of wastewater that urgently needs to be processed. Supercritical water oxidation (SCWO) technology serves as an efficient method for wastewater treatment. In this study, a SCWO experiment was carried out with organic solvent of 30% tributyl phosphate (TBP) and 70% n‐dodecane. This study investigated the operating parameters and the effects of enhanced oxidation techniques on chemical oxygen demand (COD) removal efficiency. An organic solvent SCWO process was developed, and its energy and exergy efficiencies were assessed using Aspen Plus.RESULTSThe COD removal was about 96.18% at the experimental parameters of 500 °C, 10 min, 25 MPa, oxidation coefficient of 1.5 and material concentration of 4 wt%. COD removal increased by 3.09% with the addition of CeO2. Finally, the overall energy and exergy efficiencies of the SCWO system were found to be 58.8% and 9.1% respectively by Aspen Plus.CONCLUSIONIt was found that the reaction temperature had the greatest effect on the COD removal rate compared with other reaction parameters. The decomposition of organic solvents can be divided into two stages, fast and slow, and the addition of alkali and catalyst can effectively promote the decomposition of waste organic solvents. The experiments showed that SCWO is feasible for the treatment of n‐dodecane/TBP. © 2024 Society of Chemical Industry (SCI).

Characterization of the Solution Properties of Sodium Dodecylsulphate Containing Alkaline–Surfactant–Polymer Flooding Media

Alkaline–surfactant–polymer (ASP) flooding by means of which alkali additives, surfactant and polymer are inserted as the same slug is one of the most favourable worldwide focuses of Chemical Enhanced Oil Recovery (cEOR) research and field trials, due to the individual synergy of the three chemical components. To develop efficient oil recovery chemicals, it is essential to fully understand the mechanism behind ASP flooding. Nonetheless, there are hardly any studies reporting a systematic characterization of the ASP process. Thus, the present paper focuses on modelling this process in a laboratory by the use of an anionic surfactant—sodium dodecyl sulphate (SDS) in alkaline–polymer media—which is composed of a commercial water-soluble polymer (Flopaam AN125SH®, SNF Floerger, Andrézieux-Bouthéon, France) and alkali compounds (NaOH and Na2CO3). The samples were characterized using rheometry, dynamic light scattering (DLS), infrared spectroscopy (IR) and measurement of inferfacial tension (IFT) between the samples and rapeseed oil. In accordance with the experimental results, surprisingly lower IFT values were recorded between the alkaline–polymer solutions and rapeseed oil than the samples which contained SDS. Increasing polymer and sodium chloride concentration caused a decrease (from 0.591 mN/m to 0.0486 mN/m) in IFT between the surfactant containing samples and rapeseed oil. The IR measurements confirmed that the surfactant was not detected in the oil phase in the absence of NaOH and Na2CO3. The effects of SDS on the viscosity of the mixtures were also investigated, as viscosity is a considerably important parameter in processes using polymers.

Extraction of rare earth Eu from waste blue phosphor strengthened by microwave alkali roasting

Spent phosphor is an important secondary resource for extracting rare earth elements. Microwave absorption properties and enhanced extraction of Eu from blue phosphor by microwave alkali roasting were studied. Dielectric properties of alkali roasting system were measured by resonator perturbation method. Dielectric constant increases linearly from 250 °C until it reaches a peak at 400 °C. The dielectric loss reaches a higher value at 400–550 °C, due to the strong microwave absorption properties of molten alkali and roasted products. Effects of roasting temperature, roasting time and alkali addition amount on Eu leaching were investigated. The phosphor was completely decomposed into Eu2O3, BaCO3 and MgO at 400 °C. The alkaline decomposition process of phosphor is more consistent with diffusion control model with Eα being 28.9 kJ/mol. Effects of the main leaching conditions on Eu leaching were investigated. The leaching kinetic of Eu was in line with diffusion control model with Eα being 5.74 kJ/mol. The leaching rules of rare earths in the mixed phosphor were studied. The results showed that the presence of red and green phosphor affected the recovery of blue phosphor. The optimum process parameters of rare earth recovery in single blue phosphor and mixed phosphor were obtained, and the recovery of Eu were 97.81% and 94.80%, respectively. Microwave alkali roasting promoted the dissociation of phosphor and leaching of rare earths. The results can provide reference for the efficient and selective recovery of rare earths in phosphors.

Investigation of hydrothermal depolymerization of lignite under different conditions by 13C NMR spectroscopy

Efficient depolymerization of lignite under mild conditions is the key to realizing its low carbon conversion and high value utilization. This study focuses on three Chinese lignites: Xilinguole lignite (XL), Xiaolongtan lignite (XLT), and Zhaotong lignite (ZT), investigating the inherent structures effect on their depolymerization processes when subjected to alkali depolymerization (AD) and oxidation depolymerization (OD) under hydrothermal condition. The parent lignites and their depolymerized products were characterized by solid 13C NMR, FTIR, TGA, and elemental analysis. It was found that both AD and OD effectively broke down the macromolecular structure of lignite into humic acid (HA) and small molecular products including water-soluble components, with the highest depolymerization activity observed for ZT followed by XLT and XL, regardless of the method used. Notably, by AD at 80 oC, 91.4 % of ZT was depolymerized, producing 69.4 % of HA as the major product, while higher temperatures were required to efficiently depolymerize XLT and XL by either AD or OD. More than 80% of XLT and XL can be converted by AD at 200 oC, yielding 54.8 % and 52.9 % of HA, respectively. OD at 140 oC resulted in a 57.7 % conversion of XL and an HA yield of 50.2 %. Characterization of the products demonstrated that alkali addition significantly promotes lignite depolymerization by breaking oxygen-containing linkages such as ether and ester bonds, with ether bond hydrolysis occurring predominantly at high temperatures. High-temperature AD of lignite is dominated by the cleavage of oxygen-containing linkages, whereas OD at lower temperatures mainly depolymerizes lignite through oxy-cracking of C−C and C−O weak linkages, reducing carboxyl decomposition to achieve higher HA yields. These findings offer a new perspective on the low-carbon utilization of lignite.

Strength and Compressibility Characteristics of An Expansive Soil with addition of GGBS and Alkali Activated Slag

Abstract: The phenomenal development in civil engineering infrastructure in developing countries like India, soil stabilization has emerged as à key problem in the engineering industry. Engineers have been attempting to enhance the engineering properties of low-quality soil due to their negative impact on project performance. With increasing awareness of environmental issues, there has been a remarkable shift towards green and sustainable technologies. Reuse of waste materials have been advocated for quite a while to improve the properties of poor soils open up to new avenue and double advantage of waste management. In the project investigation an attempt to evacuate the Plasticity characteristics, Strength characteristics and Compressibility characteristics were conducted on selected soil as per Indian Standards using GGBS and Alkali Activated Solution (AAS) with different percentages and curing for 0,3,7,14, and 28 days to analyze the variation of engineering properties. From the results combination of (GGBS + AAS) proved to increase of strength and reduce compressibility characteristics. The combination of GGBS + AAS is cost effective, non-destructive, low energy demanding and ecofriendly than GGBS to the selected expansive soil.

Efficient targeted acquisition 2,5-furandicarboxylic acid derived from 5-hydroxymethylfurfural over novel copper and vanadium oxide-functionalized catalysts

2,5-Furandicarboxylic acid (FDCA), which is recognized as a valuable alternative to petroleum-derived terephthalic acid and produce more bio-based polymers, has attracted considerable attention in recent years. Herein, a series of nitrogen-containing polymer nanosheets bearing Cu2+ and VO2+ (Cu2+-VO2+/PDVTA) were designed and displayed superior catalytic performance in the selective oxidation of 5-hydroxymethylfurfural (HMF) to FDCA. The catalyst was characterized by FT-IR, SEM, XPS, TG, UV–Vis DRS, PL, and ICP-AES analysis techniques. The effects of various reaction parameters, including the tert-butyl hydroperoxide dosage, temperature, and solvents on the HMF oxidation were systematically investigated, and the results were discussed in details. The Cu2+-VO2+/PDVTA catalyst achieved 100% conversion of HMF with 98.6% selectivity toward FDCA without the requirement for any basic additives under mild conditions (90 °C, 10 h), as well as has a good reusability. Coupling of the active sites of Cu2+ and VO2+ provide a synergistic effect for FDCA production. This study may provide a novel method for the development of efficient non-precious metal catalyst without addition of alkali additives, benefiting the valorization of furan-based compounds into high-valued chemicals in industrial processes.

Effects of acidification by traditional Jiaozi starter and neutralization with alkali (Na2CO3) on whole wheat dough properties.

Whole wheat steamed bread has been recommended for its potential nutritional benefits to human health. Given the positive role of both organic acid and alkali in improving dough development and product quality, the present study investigated the effects of neutralization by addition of alkali (Na2CO3) after dough acidification with traditional Jiaozi starter on the properties of whole wheat dough. The population of yeast and lactic acid bacteria and the acidification level of the dough increased significantly after fermentation with Jiaozi. Incorporation of alkali greatly improved the leavening capacity of the remixed dough and the quality of steamed bread. Jiaozi fermentation and alkali addition changed the water distribution patterns (T2) and affected the secondary structures of gluten protein, starch crystallinity and pasting properties. The storage modulus (G') of the dough increased significantly with the alkali addition, which could be attributed to the promoted cross-linking of the gluten structure and the altered hydration state of the macromolecules. The results of the present study indicate that a combination of Jiaozi fermentation and alkali addition could improve the technological properties of whole wheat dough and the quality of steamed bread. The results will help us to further explore the potential application of moderate acidification and alkali addition in the production of leavened whole wheat products. © 2024 Society of Chemical Industry.