Rising world population is expected to increase the demand for nitrogen fertilizers to improve crop yield and ensure food security. With existing challenges on low nutrient use efficiency (NUE) of urea and its environmental concerns, controlled release fertilizers (CRFs) have become a potential solution by formulating them to synchronize nutrient release according to the requirement of plants. However, the most significant challenge that persists is the “tailing” effect, which reduces the economic benefits in terms of maximum fertilizer utilization. High materials cost is also a significant obstacle restraining the widespread application of CRF in agriculture. The first part of this review covers issues related to the application of conventional fertilizer and CRFs in general. In the subsequent sections, different raw materials utilized to form CRFs, focusing on inorganic and organic materials and synthetic and natural polymers alongside their physical and chemical preparation methods, are compared. Important factors affecting rate of release, mechanism of release and mathematical modelling approaches to predict nutrient release are also discussed. This review aims to provide a better overview of the developments regarding CRFs in the past ten years, and trends are identified and analyzed to provide an insight for future works in the field of agriculture.

Research and development of nanocellulose and nanocellulose-reinforced composite materials have garnered substantial interest in recent years. This is greatly attributed to its unique functionalities and properties, such as being renewable, sustainable, possessing high mechanical strengths, having low weight and cost. This review aims to highlight recent developments in incorporating nanocellulose into rubber matrices as a reinforcing filler material. It encompasses an introduction to natural and synthetic rubbers as a commodity at large and conventional fillers used today in rubber processing, such as carbon black and silica. Subsequently, different types of nanocellulose would be addressed, including its common sources, dimensions, and mechanical properties, followed by recent isolation techniques of nanocellulose from its resource and application in rubber reinforcement. The review also gathers recent studies and qualitative findings on the incorporation of a myriad of nanocellulose variants into various types of rubber matrices with the main goal of enhancing its mechanical integrity and potentially phasing out conventional rubber fillers. The mechanism of reinforcement and mechanical behaviors of these nanocomposites are highlighted. This article concludes with potential industrial applications of nanocellulose-reinforced rubber composites and the way forward with this technology.

Inclusion of the two isomers of citral (E-citral and Z-citral), components of lemongrass oil, was investigated within the confines of various cyclodextrin (α-CD, β-CD and γ-CD) host molecules. Aqueous complex formation constants for E-citral with α-CD, β-CD and γ-CD were determined to be 123, 185, and 204 L/mol, respectively, whereas Z-citral exhibited stronger affinities (157, 206, and 253 L/mol, respectively). The binding trend γ-CD > β-CD > α-CD is a reflection of the more favorable geometrical accommodation of the citral isomers with increasing cavity size. Encapsulation of lemongrass oil within CDs was undertaken through shaking citral:CD (1:1, 1.5:1, and 2:1 molar ratio) mixtures followed by spray drying. Maximum citral retention occurred at a 1:1 molar ratio with β-CD and α-CD demonstrating the highest levels of total E-citral and Z-citral retention, respectively. Furthermore, the β-CD complex demonstrated the slowest release rate of all inclusion complex powders.

This study aims to investigate the role of hydrogen on CNTs synthesis and kinetics of CNTs formation. The CNTs were synthesized by catalytic chemical vapor deposition of methane over FeMo/MgO catalyst. The experimental results revealed that hydrogen plays an important role in the structural changes of catalyst during the pre-reduction process. The catalyst structure fully transformed into metallic FeMo phases, resulting in an increased yield of 5 folds higher than those of the non-reduced catalyst. However, the slightly larger diameter and lower crystallinity ratio of CNTs was obtained. The hydrogen co-feeding during the synthesis can slightly increase the CNTs yield. After achieving the optimum amount of hydrogen addition, further increase in hydrogen would inhibit the methane decomposition, resulting in lower product yield. The hydrogenation of carbon to methane was proceeded in hydrogen co-feed process. However, the hydrogenation was non-selective to allotropes of carbon. Therefore, the addition of hydrogen would not benefit neither maintaining the catalyst stability nor improving the crystallinity of the CNT products. The kinetic model of CNTs formation, derived from the two types of active site of dissociative adsorption of methane, corresponded well to the experimental results. The rate of CNTs formation greatly increases with the partial pressure of methane but decreases when saturation is exceeded. The activation energy was found to be 13.22 kJ mol⁻¹, showing the rate controlling step to be in the process of mass transfer.