Matches in SemOpenAlex for { <https://semopenalex.org/work/W4386836139> ?p ?o ?g. }
Showing items 1 to 74 of
74
with 100 items per page.
- W4386836139 abstract "Purpose In this study, solid formaldehyde, benzoguanamine and butanol were used to synthesize butylated benzo-amino resin by one-step-two-stage method. Design/methodology/approach This research first examined the influence of solid formaldehyde content on the hydroxymethylation phase. Subsequently, the effects of butanol content, etherification time and hydrochloric acid content on the formation of benzo-amino resin during the etherification stage were studied in detail. In addition, the reaction process was further analyzed through interval sampling withdrawing during the hydroxymethylation and etherification stages. Finally, the synthesized benzo-amino resins were used in the production of high solid content polyester and acrylic coatings and the properties of that were also evaluated. Findings Based on the experimental findings, the authors have successfully determined the optimal process conditions for the one-step-two-stage method in this study. The hydroxymethylation stage demonstrated the most favorable outcomes at a reaction temperature of 60°C and a pH of 8.5. Similarly, for the etherification stage, the optimal conditions were achieved at a temperature of 45°C and a pH of 4.5. Furthermore, the investigation revealed that a ratio of benzoguanamine to solid formaldehyde to n-butanol, specifically at 1:5.2:15, produced the best results. The performance of the resulting etherified benzo-amino resin was thoroughly evaluated in high solid content coatings, and it exhibited promising characteristics. Notably, there was a significant enhancement in the water resistance, solvent resistance and glossiness of canned iron printing varnish coatings. Originality/value Amino resin, a versatile chemical compound widely used in various industries, presents challenges in terms of sustainability and operational efficiency when synthesized using conventional methods, primarily relying on a 37% formaldehyde solution. To address these challenges, the authors propose a novel approach in this study that combines the advantages of the solid formaldehyde with a two-stage catalytic one-step synthesis process. The primary objective of this research is to minimize the environmental impact associated with amino resin synthesis, optimize resource utilization and enhance the economic feasibility for its industrial implementation. By adopting this alternative approach, the authors aim to contribute toward a more sustainable and efficient production of amino resin." @default.
- W4386836139 created "2023-09-19" @default.
- W4386836139 creator A5000749198 @default.
- W4386836139 creator A5005348559 @default.
- W4386836139 creator A5038442604 @default.
- W4386836139 creator A5041351237 @default.
- W4386836139 creator A5081288331 @default.
- W4386836139 creator A5088973373 @default.
- W4386836139 date "2023-09-19" @default.
- W4386836139 modified "2023-09-26" @default.
- W4386836139 title "Synthesis of butylated benzo-amino resin by solid formaldehyde one-step-two-stage method and its application in high solid content coatings" @default.
- W4386836139 cites W1965485919 @default.
- W4386836139 cites W1982196237 @default.
- W4386836139 cites W2021720746 @default.
- W4386836139 cites W2034964025 @default.
- W4386836139 cites W2080471837 @default.
- W4386836139 cites W2080972505 @default.
- W4386836139 cites W2145008285 @default.
- W4386836139 cites W2749243691 @default.
- W4386836139 cites W3018052687 @default.
- W4386836139 cites W3081696446 @default.
- W4386836139 cites W3091907531 @default.
- W4386836139 cites W3153338944 @default.
- W4386836139 cites W4229490129 @default.
- W4386836139 cites W4281818786 @default.
- W4386836139 cites W4313595919 @default.
- W4386836139 cites W4323073143 @default.
- W4386836139 doi "https://doi.org/10.1108/prt-05-2023-0043" @default.
- W4386836139 hasPublicationYear "2023" @default.
- W4386836139 type Work @default.
- W4386836139 citedByCount "0" @default.
- W4386836139 crossrefType "journal-article" @default.
- W4386836139 hasAuthorship W4386836139A5000749198 @default.
- W4386836139 hasAuthorship W4386836139A5005348559 @default.
- W4386836139 hasAuthorship W4386836139A5038442604 @default.
- W4386836139 hasAuthorship W4386836139A5041351237 @default.
- W4386836139 hasAuthorship W4386836139A5081288331 @default.
- W4386836139 hasAuthorship W4386836139A5088973373 @default.
- W4386836139 hasConcept C127413603 @default.
- W4386836139 hasConcept C178790620 @default.
- W4386836139 hasConcept C185592680 @default.
- W4386836139 hasConcept C192562407 @default.
- W4386836139 hasConcept C2775930285 @default.
- W4386836139 hasConcept C2777436746 @default.
- W4386836139 hasConcept C2780471494 @default.
- W4386836139 hasConcept C2781448156 @default.
- W4386836139 hasConcept C28667232 @default.
- W4386836139 hasConcept C42360764 @default.
- W4386836139 hasConceptScore W4386836139C127413603 @default.
- W4386836139 hasConceptScore W4386836139C178790620 @default.
- W4386836139 hasConceptScore W4386836139C185592680 @default.
- W4386836139 hasConceptScore W4386836139C192562407 @default.
- W4386836139 hasConceptScore W4386836139C2775930285 @default.
- W4386836139 hasConceptScore W4386836139C2777436746 @default.
- W4386836139 hasConceptScore W4386836139C2780471494 @default.
- W4386836139 hasConceptScore W4386836139C2781448156 @default.
- W4386836139 hasConceptScore W4386836139C28667232 @default.
- W4386836139 hasConceptScore W4386836139C42360764 @default.
- W4386836139 hasLocation W43868361391 @default.
- W4386836139 hasOpenAccess W4386836139 @default.
- W4386836139 hasPrimaryLocation W43868361391 @default.
- W4386836139 hasRelatedWork W1986117761 @default.
- W4386836139 hasRelatedWork W1986974960 @default.
- W4386836139 hasRelatedWork W2024053618 @default.
- W4386836139 hasRelatedWork W2043757586 @default.
- W4386836139 hasRelatedWork W2056492924 @default.
- W4386836139 hasRelatedWork W2084701745 @default.
- W4386836139 hasRelatedWork W2500742033 @default.
- W4386836139 hasRelatedWork W2604662488 @default.
- W4386836139 hasRelatedWork W2748952813 @default.
- W4386836139 hasRelatedWork W2899084033 @default.
- W4386836139 isParatext "false" @default.
- W4386836139 isRetracted "false" @default.
- W4386836139 workType "article" @default.