Clay minerals surfaces potentially play a role in prebiotic synthesis through adsorption of organic monomers that give rise to highly concentrated systems; facilitate condensation and polymerization reactions, protection of early biomolecules from hydrolysis and photolysis, and surface-templating for specific adsorption and synthesis of organic molecules. This review presents processes of clay formation using saponite as a model clay mineral, since it has been shown to catalyze organic reactions, is easy to synthesize in large and pure form, and has tunable properties. In particular, a method involving urea is presented as a reasonable analog of natural processes. The method involves a two-step process: (1) formation of the precursor aluminosilicate gel and (2) hydrolysis of a divalent metal (Mg, Ni, Co, and Zn) by the slow release of ammonia from urea decomposition. The aluminosilicate gels in the first step forms a 4-fold-coordinated Al similar to what is found in nature such as in volcanic glass. The use of urea, a compound figuring in many prebiotic model reactions, circumvents the formation of undesirable brucite, Mg(OH), in the final product, by slowly releasing ammonia thereby controlling the hydrolysis of magnesium. In addition, the substitution of B and Ga for Si and Al in saponite is also described. The saponite products from this urea-assisted synthesis were tested as catalysts for several organic reactions, including Friedel-Crafts alkylation, cracking, and isomerization reactions.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555627PMC
http://dx.doi.org/10.3390/life10090168DOI Listing

Publication Analysis

Top Keywords

urea-assisted synthesis
8
organic reactions
8
reactions
5
synthesis characterization
4
saponite
4
characterization saponite
4
saponite octahedral
4
octahedral tetrahedral
4
tetrahedral metals
4
metals review
4

Similar Publications

The urgent need to address escalating environmental pollution and energy management challenges has underscored the importance of developing efficient, cost-effective, and multifunctional electrocatalysts. To address these issues, we developed an eco-friendly, cost-effective, and multifunctional electrocatalyst a solvothermal synthesis approach. Due to the merits of the ideal synthesis procedure, the FeCoHS@NF electrocatalyst exhibited multifunctional activities, like OER, HER, OWS, UOR, OUS, and overall alkaline seawater splitting, with required potentials of 1.

View Article and Find Full Text PDF

Pyrazole-Mediated On-Surface Synthesis of Nickel/Nickel Oxide Hybrids for Efficient Urea-Assisted Hydrogen Production.

Nano Lett

January 2025

Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials and Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), Fudan University, Shanghai 200438, China.

Creating densely functionalized supported materials without aggregation has been one of the ultimate goals for heterogeneous catalysts. Direct conversion of readily available bulk materials into highly dispersed supported materials could be highly beneficial for real applications. In this work, we invented an on-surface synthetic strategy for generating highly loaded and well-dispersed nickel nanoparticles on nickel oxide supports (Ni/NiO).

View Article and Find Full Text PDF

Tailoring C-defect O-doping and n-π* transition awakened porous ultra-thin carbon nitride for efficient peroxymonosulfate activation: Performances and mechanism insight.

J Environ Sci (China)

June 2025

Key Laboratory of Preparation and Application of Environmental Friendly Materials, Ministry of Education, Jilin Normal University, Changchun 130103, China; College of Chemistry, Jilin Normal University, Siping 136000, China.

Integrating photocatalysis technology with peroxymonosulfate oxidation possesses huge potential for degrading stubborn pollutant. Herein, a porous ultra-thin carbon nitride with C-defect O-doping and advanced n-π* transition was customized by one-pot thermal-induced polymerization of molten urea assisted with paraformaldehyde. Via visible-light coupling peroxymonosulfate activation, the DCN-100 can completely photodegrade 2,4-dichlorophenol, and rate constant is 136.

View Article and Find Full Text PDF

Iron nitrides with the merits of high theoretical capacities, cost-effectiveness, and good electronic/ionic conductivity have been recognized as attractive anode candidates for lithium-ion batteries (LIBs). Carbon compositing, pore engineering, and nanostructure construction have proved to be effective strategies to prepare high-performance metal nitride anodes for LIBs. Herein, we synthesized a series of FeN-embedded and N-doped carbon nanorods (FeN@NCNR) with a hierarchical porous system and controllable topography by metal-catalyzed graphitization-nitridization of the Fe(III)-triazole framework (Fe-MOF) and thermal evaporation of the triblock copolymer F127 template assembled in Fe-MOF via hydrogen bonding interaction, followed by the air oxidation and urea-assisted ammonolysis processes.

View Article and Find Full Text PDF

Fabrication of Ternary Titanium Dioxide/Polypyrrole/Phosphorene Nanocomposite for Supercapacitor Electrode Applications.

Molecules

May 2024

Department of Materials Science and Engineering, Soongsil University 369, Sangdo-ro, Dongjak-gu, Seoul 06978, Republic of Korea.

In this paper, we report a titanium dioxide/polypyrrole/phosphorene (TiO/PPy/phosphorene) nanocomposite as an active material for supercapacitor electrodes. Black phosphorus (BP) was fabricated by ball milling to induce a phase transition from red phosphorus, and urea-functionalized phosphorene (urea-FP) was obtained by urea-assisted ball milling of BP, followed by sonication. TiO/PPy/phosphorene nanocomposites can be prepared via chemical oxidative polymerization, which has the advantage of mass production for a one-pot synthesis.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!