Comparison of the activities of C2N and BCNO towards Congo red degradation

An n-type organic carbon nitride semiconductor, C2N, was synthesized by the pyrolysis of uric acid, and its properties were investigated by scanning electron and transmission electron microscopies, X-ray powder diffraction, and vibrational, UV-visible and X-ray photoelectron spectroscopies. This novel material, composed of crystalline flakes, featured a broad absorption centered at 700¿nm, possibly due to charge transfer, and a 2.49¿eV band gap. Its catalytic performance was assessed for the treatment of effluents with the diazo dye Congo red, comparing it with that of boron carbon nitrogen oxide, BCNO. Both wide band gap semiconductors exhibited decolorizing activity in the dark, although the mechanisms were different and were not photocatalytic: BCNO was more effective towards the adsorption-coordination due to the presence of B-O, while C2N was effective towards the adsorption and the advancement of the oxidation reaction. Their kinetic constants (0.19 and 0.02 min-1 for BCNO and C2N, respectively) were comparable to those of intermetallic compounds studied for azo dyes degradation in dark conditions. In view of the high color removal efficiency (97% after 20¿min) and good reusability of BCNO, this study suggests a potential application of this catalyst for wastewater treatment, alone or in combination with C2N

Visible Light Responsive Strontium Carbonate Catalyst Derived from Solvothermal Synthesis

A single crystalline phase of strontium carbonate (SrCO3) was successfully obtained from solvothermal treatments of hydrated strontium hydroxide in ethanol (EtOH) at 100 °C for 2 h, using specific Sr:EtOH mole ratios of 1:18 or 1:23. Other solvothermal treatment times (0.5, 1.0 and 3 h), temperatures (80 and 150 °C) and different Sr:EtOH mole ratios (1:13 and 1:27) led to formation of mixed phases of Sr-containing products, SrCO3 and Sr(OH)2 xH2O. The obtained products (denoted as 1:18 SrCO3 and 1:23 SrCO3), containing a single phase of SrCO3, were further characterized in comparison with commercial SrCO3, and each SrCO3 material was employed as a photocatalyst for the degradation of methylene blue (MB) in water under visible light irradiation. Only the 1:23 SrCO3 sample is visible light responsive (Eg = 2.62 eV), possibly due to the presence of ethanol in the structure, as detected by thermogravimetric analysis. On the other hand, the band gap of 1:18 SrCO3 and commercial SrCO3 are 4.63 and 3.25 eV, respectively, and both samples are UV responsive. The highest decolourisation efficiency of MB solutions was achieved using the 1:23 SrCO3 catalyst, likely due to its narrow bandgap. The variation in colour removal results in the dark and under visible light irradiation, with radical scavenging tests, suggests that the high decolourisation efficiency was mainly due to a generated hydroxyl-radical-related reaction pathway. Possible degradation products from MB oxidation under visible light illumination in the presence of SrCO3 are aromatic sulfonic acids, dimethylamine and phenol, as implied by MS direct injection measurements. Key findings from this work could give more insight into alternative synthesis routes to tailor the bandgap of SrCO3 materials and possible further development of cocatalysts and composites for environmental applications

Modified Starch-Based Adhesives: A Review

Consumer trends towards environmentally friendly products are driving plastics industries to investigate more benign alternatives to petroleum-based polymers. In the case of adhesives, one possibility to achieve sustainable production is to use non-toxic, low-cost starches as biodegradable raw materials for adhesive production. While native starch contains only hydroxyl groups and has limited scope, chemically modified starch shows superior water resistance properties for adhesive applications. Esterified starches, starches with ester substituents, can be feasibly produced and utilized to prepare bio-based adhesives with improved water resistance. Syntheses of esterified starch materials can involve esterification, transesterification, alkylation, acetylation, succinylation, or enzymatic reactions. The main focus of this review is on the production of esterified starches and their utilization in adhesive applications (for paper, plywood, wood composites, fiberboard, and particleboard). The latter part of this review discusses other processes (etherification, crosslinking, grafting, oxidation, or utilizing biobased coupling agents) to prepare modified starches that can be further applied in adhesive production. Further discussion on the characteristics of modified starch materials and required processing methods for adhesive production is also included

Insight into the Molecular Weight of Hydrophobic Starch Laurate-Based Adhesives for Paper

Instead of using finite petroleum-based resources and harmful additives, starch can be used as a biodegradable, low-cost, and non-toxic ingredient for green adhesives. This work employs K3PO4 catalyzed transesterifications of cassava starch and methyl laurate at varying reaction times (1–10 h), resulting in the enhanced hydrophobicity of starch laurates. At longer reaction times, starch laurates having higher degrees of substitution (DS) were obtained. While starch laurates are the major products of transesterification, relatively low-molecular-weight byproducts (1%) were detected and could be hydrolyzed starches based on gel permeation chromatography results. Contact angle measurements confirmed the relatively high hydrophobicity of the modified starches compared with that of native starch. The modified starches were then employed to prepare water-based adhesives on paper (without any additional additives). Notably, the shear strength of the esterified starch adhesives appears to be independent of the DS of esterified samples, hence the transesterification reaction times. Additionally, the shear strength of water-based adhesives (0.67–0.73 MPa) for bonding to paper substrates is superior to that of two other commercially available glues by a factor of 10 to 80 percent

Identification of Active Species in Photodegradation of Aqueous Imidacloprid over g-C₃N₄/TiO₂ Nanocomposites

In this work, g-C3N4/TiO2 composites were fabricated through a hydrothermal method for the efficient photocatalytic degradation of imidacloprid (IMI) pesticide. The composites were fabricated at varying loading of sonochemically exfoliated g-C3N4 (denoted as CNS). Complementary characterization results indicate that the heterojunction between the CNS and TiO2 formed. Among the composites, the 0.5CNS/TiO2 material gave the highest photocatalytic activity (93% IMI removal efficiency) under UV-Vis light irradiation, which was 2.2 times over the pristine g-C3N4. The high photocatalytic activity of the g-C3N4/TiO2 composites could be ascribed to the band gap energy reduction and suppression of photo-induced charge carrier recombination on both TiO2 and CNS surfaces. In addition, it was found that the active species involved in the photodegradation process are OH• and holes, and a possible mechanism was proposed. The g-C3N4/TiO2 photocatalysts exhibited stable photocatalytic performance after regeneration, which shows that g-C3N4/TiO2 is a promising material for the photodegradation of imidacloprid pesticide in wastewater

Synergistic effects between acidity and the crystalline phases of thermally activated layered Zn hydroxide nitrate on the methanolysis of acidic soybean oils

Layered hydroxyl salts (LHS) is a promising catalyst in the field of methanolysis (transesterification and esterification reactions) of oil feedstocks. The catalytic activity of the catalyst can be enhanced with heat treatment. The present study investigated the relationship between thermal stability of the layered Zn hydroxide nitrate (ZHN), their acid-base properties, and the catalytic conversion of oil feedstocks to methyl ester. The solid, predominantly acidic catalyst was prepared at various temperatures (70–170 °C) and tested for the acidic/basic properties using the Hammett indicators and titration method followed by functional group analysis using FTIR, crystallization using X-ray diffraction, and surface morphology using SEM. The combination of various characterization techniques gave an insight into the changes in the phases of the layered Zn hydroxide nitrate catalysts upon thermal treatment. Major phase changes occurred at temperatures somewhat above 80, and 140 °C. The catalysts were extensively studied to understand the underlying effects on the FAME yields obtained from catalytic conversion of oleic acid spiked soy bean oil (a model of an acidic oil feedstock) into methyl esters. The results of the optimization reactions reaffirmed the effect of the phase changes when the highest FAME yield was observed from two activated samples namely, Zn5_80 and Zn5_140. The optimized reactions condition of catalytic conversion of SO containing 10% OA at 5 °C/min heating rate, 3 wt % catalyst concentration, 30:1 methanol to oil molar ratio, reaction time of 100 °C for 2 h gave 92% FAME yield when Zn5_140 was used as the catalyst. The detected of the single phase of Zn5(OH)8(NO3)2 in Zn5_80, Zn5(OH)8(NO3)2 and ZnO in Zn5_140 (2-phase system), including Zn5(OH)8(NO3)2, Zn3(OH)4(NO3)2, and ZnO in Zn5_170 (3-phase system), suggested all three phases contributes to the high catalytic activity in methanolysis of the acidic oils. Both Zn5_140 and Zn5_170 gave a comparably high FAME yields based on statistical analyses. This study ascertained the synergistic effects of the high acidity (>0.4 mmol/g) and the dominant active phases of the thermally treated layered Zn hydroxide nitrate on the high catalytic activity that favours esterification of acidic oil feedstocks

Antifungal Activity of Water-Based Adhesives Derived from Pineapple Stem Flour with Apple Cider Vinegar as an Additive

As a byproduct of bromelain extraction procedures, pineapple stem flour is underutilized. Since water glues derived from gelatinization typically have poor mold resistance, this study aims to produce flour-based value-added products, such as mold-resistant water-based adhesives. To address this issue, this study explored the use of apple cider vinegar (ACV) as a low-cost, non-toxic, commercially available antifungal agent to improve the mold resistance of adhesives. Furthermore, laurate flour was produced via a transesterification of the flour and methyl laurate using a K2CO3 catalyst. Both the unmodified flour and the functionalized flour were employed to prepare water-based adhesives. For both flour systems, adding ACV at concentrations of at least 2.0% v/v enhanced the mold resistance of the adhesives and completely inhibited the development of A. niger mycelia for up to 90 days of storage. The adhesives made from the transesterified flour exhibited a higher shear strength for the paper bonding (ca. 8%) than the unmodified ones. Additionally, the ACV additive had no negative effects on the shear strengths of the water-based adhesives. All of the flour-based adhesives developed in this study had a higher shear strength for paper substrates than two locally available commercial water glues

Magnetically Recoverable Biomass-Derived Carbon-Aerogel Supported ZnO (ZnO/MNC) Composites for the Photodegradation of Methylene Blue

Hydrothermally assisted magnetic ZnO/Carbon nanocomposites were prepared using the selective biowaste of pomelo orange. Initially, the carbon aerogel (CA) was prepared hydrothermally followed by a freeze-drying method. Furthermore, the iron oxide nanoparticles were deposited onto the surface of carbon using the co-precipitation method and we obtained magnetic carbon nanocomposite, i.e., Fe3O4/C (MNC). Moreover, the ZnO photocatalysts were incorporated onto the surface of MNC composites using a hydrothermal process, and we obtained ZnO/MNC composites. The ZnO/MNC (55%), ZnO/MNC (65%) and ZnO/MNC (75%) composites were prepared by a similar experimental method in order to change the weight ratio of ZnO NPs. Using a similar synthetic procedure, the standard ZnO and Fe3O4 nanoparticles were prepared without the addition of CA. The experimental results were derived from several analytical techniques, such as: X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman and diffuse reflectance spectroscopy (DRS-UV). The synthesized carbon, ZnO, Fe3O4, ZnO/MNC (55%), ZnO/MNC (65%) and ZnO/MNC (75%) composites were examined through the photocatalytic degradation of methylene blue (MB) under visible-light irradiation (VLI). The obtained results revealed that the composites were more active than carbon, ZnO and Fe3O4. In particular, the ZnO/MNC (75%) composites showed more activity than the rest of the composites. Furthermore, the recycling abilities of the prepared ZnO/MNC (75%) composites were examined through the degradation of MB under identical conditions and the activity remained constant up to the fifth cycle. The synthetic procedure and practical applications proposed here can be used in chemical industries, biomedical fields and energy applications

Fabrication of Hydrotalcite-like Copper Hydroxyl Salts as a Photocatalyst and Adsorbent for Hexavalent Chromium Removal

Cu-HyS-urea and Cu-HyS-NaOH, which are hydrotalcite-like copper hydroxyl salts, were prepared by two different methods, urea hydrolysis and precipitation, respectively. Both synthesis methods provided the successful formation of a copper hydroxyl salt, Cu2(OH)3NO3. From XRD and UV-DRS results, the product from the urea hydrolysis methods (Cu-HyS-urea) displayed higher crystallinity, small bandgap energy (Eg), and high light absorption ability because of some intercalated carbonate anions. For the Cr(VI) removal test, the Cu-HyS-NaOH showed superior adsorption of Cr(VI) than Cu-HyS-urea due to a higher specific surface area, confirmed by BET analysis. However, the Cu-HyS-urea presented higher photocatalytic Cr(VI) reduction under light irradiation than Cu-HyS-NaOH, owing to narrow Eg, less recombination, and a high transfer of the photogenerated charge carriers, proven by the results from photoluminescence, photocurrent density, and electrochemical impedance spectroscopy. Thus, this work provides a new function of the hydrotalcite-like copper hydroxyl salts (Cu-HyS-urea and Cu-HyS-NaOH) that can be utilized not only for adsorption of Cr(VI) but also as photocatalysts for Cr(VI) reduction under light irradiation