Urea Release Research Articles

A Biopolymer Coating Strategy for the Slow Release of Urea from Urea Fertiliser

A Biopolymer Coating Strategy for the Slow Release of Urea from Urea Fertiliser

Effect of N,N′-Methylenebisacrylamide on properties of porous semi-IPN hydrogels from Acrylamide, Maleic Acid, and its use for Urea absorption

Hydrogel is a three-dimensional polymer that can absorb large amounts of reagents while maintaining structural integrity. This material has been applied in many fields especially in smart agriculture. To improve the economic viability, the reusability of hydrogels in agricultural engineering over multiple cycles of adsorption and desorption is an urgent requirement. This can be solved if the crosslinker is used properly. Therefore, in this work, a series of porous semi-IPN hydrogels based on linear polyacrylamide, acrylamide, maleic acid, and N,N′-methylenebisacrylamide (MBA) were synthesized. The hydrogels were evaluated for the impact of MBA content on the characteristics and applicability as a urea fertilizer carrier. The chemical composition, morphology, mechanical, and rheological properties, swelling behavior, urea absorption and desorption of hydrogels with crosslinker content in the range of 0.5-2.0 % were investigated. The porous structure was confirmed by scanning electron microscopy images. Changing the MBA content significantly affected all characteristics of the hydrogels. In particular, increasing the MBA content decreased the equilibrium swelling ratios in all investigated environments. The maximum amount of urea loaded into the hydrogel was also reduced from 435.88 to 188.50 mg/g. This increase also changed the swelling mechanism from non-Fickian to Fickian, whereas the urea release mechanism changed from Fickian to non-Fickian. Finally, the hydrogels demonstrated stability in soil over multiple cycles of water absorption and release. This study provides valuable insights into designing a semi-IPN hydrogel with desired properties that meet the application requirements of modern farming techniques.

Assembly of Silicate-Phenolic Network Coatings with Tunable Properties for Controlled Release of Small Molecules.

Engineered coatings are pivotal for tailoring the surface properties and release profiles of materials for applications across diverse areas. However, developing robust coatings that can both encapsulate and controllably release cargo is challenging. Herein, a dynamic covalent coordination assembly strategy is used to engineer robust silicate-based coatings, termed silicate-phenolic networks (SPNs), using sodium metasilicate and phenolic ligands (tannic acid, gallic acid, pyrogallol). The coatings are pH-responsive (owing to the dynamic covalent bonding), and their hydrophobicity can be tuned upon their post-functionalization with hydrophobic gallates (propyl, octyl, lauryl gallates). The potential of the SPN coatings for the controlled release of small molecules, such as urea (a widely used fertilizer), is demonstrated-controlled release of urea in soil is achieved in response to different pHs (up to 7 days) and different hydrophobicity (up to 14 days). Furthermore, leveraging the presence of silicon (within the coating) and post-functionalization of the SPN coatings with metal ions (Fe3+, Cu2+, Zn2+) generates a multipurpose delivery system for the sustained release of micronutrient fertilizers, and silicon and metal ions, over 28 and 14 days, respectively. These SPN coatings have potential applications beyond agriculture, including nutrient delivery, separations, food packaging, and medical device fabrication.

Ionically crosslinked Sodium alginate – Galactoxyloglucan hydrogel beads as a controlled release system for sustainable urea delivery

The prolonged usage of chemical fertilizers often causes deleterious effects on the environment, and it remains an alarming issue in agricultural practices. Smart delivery of fertilizers achieved by hydrogels proved their efficiency in reducing risk in action. In this study, we investigated the optimization of urea-encapsulated hydrogel formulations and evaluated their physical and chemical attributes for agricultural applications. The proposed hydrogel formulation consists of ionically crosslinked two promising plant biopolymers (galactoxyloglucan and sodium alginate) which are specifically developed for the controlled release of urea fertilizer. The FT-IR analysis of the hydrogel beads confirmed the presence of biopolymer functional groups and urea. XRD analysis indicated the amorphous nature of the biopolymers. TGA revealed a thermal stability of up to 350°C. SEM images showed the porous structure of the hydrogel beads. To investigate the controlled release of urea, two kinetic models were employed: Korsmeyer-Peppas and Peppas-Sahlin. The results indicated a controlled release mechanism. The hydrogel beads demonstrated excellent water retention properties, maintaining soil moisture for up to 16 days. Additionally, degradability results demonstrated that in the soil environment, the hydrogel beads were degraded completely in 21 days. Therefore, we are confident that the formulated hydrogel bead exhibits eco-friendly and bio-compatible characteristics, which potentially mitigate the risks associated with urea fertilizers.

PSLBI-9 The growth performance and total tract starch digestibility of finishing Nelore bulls fed flint corn-based diets are improved by the corn processing method and urea source

Abstract The aim of this study was to evaluate the flint corn processing method (CPM) and urea source for finishing Nellore bulls fed corn-based diets. In this study, 80 Nellore bulls [initial body weight (BW) = 388 ± 45.7 kg] were allocated into 28 pens (7 pens/treatment; 6 pens with 3 bulls + 1 pen with 2 bulls). A completely randomized design with a 2 × 2 factorial arrangement of treatments was used to test two CPMs: dry ground corn (DGC) and reconstituted and ensiled corn (REC), and two US: feed-grade urea (FGU) and post-ruminal release urea (PRU). Dietary inclusion (% DM) of flint corn (vitreousness = 86.0%) was 61.3% (DGC or REC), and urea source addition was 0.5% as non-protein nitrogen (NPN; as FGU or PRU). The PRU source (Trouw Nutrition, Netherlands) contained 82% urea on a DM basis. In an in vitro assay, 27% of this urea was released into the rumen. Experimental period lasted 100 d (with 14 d of adaptation). Fecal samples from each bull were collected in two periods of three consecutive days (d 44 to 46 and 94 to 96) at different time (0600, 1200, and 1800 h). Samples were composited by pen and analyzed for fecal starch (FS) and indigestible NDF as markers for fecal excretion. At the end of the experiment, bulls were slaughtered and the jejunum and pancreas were sampled from one bull per pen. Interaction effects were not found (P ≥ 0.31) for any feedlot growth performance variables (Table 1). Final BW, average daily gain, and feed efficiency (gain to feed; G:F) were greater for bulls fed REC and PRU than for those fed DGC and FGU (P < 0.02), respectively. As a result, observed dietary net energy (NE) for maintenance and BW gain were about 7.0% and 9.0% greater for bulls fed REC diets, and 4.3% and 5.6% greater for bulls fed PRU diets, respectively. Bulls fed DGC had 2.2 times greater FS compared with bulls fed REC, resulting in lower fecal pH and total tract starch digestibility (TSD) for bulls fed DGC compared with those fed REC (P < 0.01). Interestingly, a similar trend was observed in bulls fed PRU compared with those fed diets with FGU (P < 0.06). Jejunal gene expression of SLC5A1 was not affected by treatments (P > 0.14). Nevertheless, bulls fed diets with PRU presented greater jejunal α-amylase activity (P = 0.02). Pancreatic α-amylase activity was less when bulls were fed DGC + PRU diet. In conclusion, REC markedly improved TSD and growth performance compared with DGC. Additionally, independent of CPM, PRU inclusion as NPN source increased G:F and dietary NE concentration due to the positive effects on jejunal amylase activity and TSD.

Novel biopolymeric chitosan-urea-based core-shell hydrogel for use in sustainable agriculture

Agricultural sustainability is a major issue in recent times, deficiency of water as well as insufficient fertilizer to the crop is a main reason for it. This work is focused on core-shell hydrogel aiming to overcome the agricultural issues of water as well as deficiency of fertilizer to the plant. The core-shell hydrogel was prepared by incorporating urea in κ-carrageenan to be part of the controlled release mechanism of the core of the hydrogel. Chitosan was used for the shell structure to prepare over the core and cross-linked by the cations of the salts. The prepared hydrogel was termed as Chitosan-κ-carrageenan-Urea (CK-CU). Four different types of hydrogels were prepared with the different compositions named as CK-CU 2, CK-CU 5, CK-CU 7.5 and CK-CU 10 as varying with the ratio of 2 %, 5 %, 7.5 % and 10 % of urea respectively. The core-shell morphology structure was verified with Scanning electron microscopy (SEM) in which the complete coverage of the κ-carrageenan core by a consistent chitosan shell has been verified. Fourier transform infrared spectroscopy (FTIR) was utilized to confirm the composition of the hydrogel. Thermo-gravimetric analysis (TGA) was also performed for checking the thermal endurance of the hydrogel. The release rate of the urea was determined under Ultraviolet Visible spectroscopy. The swelling index, dewatering, and urea release rate of optimized CK-CU 10 hydrogel were found to 121 %, 21.22 %, and 70.4 % respectively. The developed Core-Shell hydrogel exhibits significant promise as a vehicle for fertilizer and as a soil conditioner in agricultural applications especially in arid and semi-arid areas.

Environmentally friendly slow-release urea fertilizer based on modified chitosan membrane

The inefficient use of conventional fertilizers has prompted the exploration of slow-release fertilizer (SRF) systems to enhance plant nutrient delivery and uptake. This study investigates the potential of the chitosan (CS) membrane modified with succinic acid (SA) and calcium ions (Ca2+) as an effective SRF system. The CS/SA-U/Ca-coated membrane can extend the release period of urea, thereby optimizing fertilizer efficiency and promoting plant growth. The structural and chemical features of the CS/SA-U/Ca membrane were comprehensively analyzed. The modification with Ca2+ increased the membrane’s thickness, decreased its swelling degree, and resulted in a rougher, more porous surface, all of which contributed to a more controlled release of urea. Urea release profiles were evaluated in both water and soil, demonstrating that the CS/SA-U/Ca coating extended the release period to 20 days in water and over 30 days in soil. Quantitative UV–Vis spectrophotometry and qualitative assessments were used to measure the urea release and evaluate the impact of the SRF on vegetable plant growth. Experimental results demonstrated a significant enhancement in plant growth, with a 46 % increase in stem growth and a doubling of leaf count compared to control plants without the SRF membrane. These findings suggest that the CS/SA-U/Ca-coated SRF system holds promise for optimizing fertilizer use and promoting plant growth by providing a more controlled nutrient release.

Preparation and characterization of starch carbamate modified natural sodium alginate composite hydrogel blend formulation and its application for slow-release fertilizer

The exploration of environmentally friendly slow-release fertilizer (SRF) based on natural bio-polymers is of great importance in the development of modern agriculture and horticulture. Herein, a novel starch carbamate (SC) modified sodium alginate (SA) hydrogel (SC/SAH) was prepared utilizing as-synthesized SC and natural SA through the cationic ions crosslinking method and ultimately the corresponding slow-release fertilizer (SC/SAH-SRF) was successfully developed by immersing the dried SC/SAH matrix into saturated urea solution. Due to the low gelation temperature and high viscosity of the synthesized SC, the formed SC/SAH exhibits significantly enhanced properties including excellent water absorbency up to 8.02 g/g with considerable repeatability, abundant pore structure and high hydrophilicity compared with the neat SAH and natural starch based hydrogel (NS/SAH). Accordingly, the SC/SAH leads to higher urea loading amount ∼ 1.28 g/g. Importantly, the resultant SC/SAH-SRF also shows superior slow-release performance, yielding a cumulative urea release of only 61.6 % within 10 h and almost completely release >16 h in water, what's more, only 58.5 % of the urea releases within 25 days and exceeding 50 days for complete release in soil column assays. The slow-release of urea from SC/SAH-SRF well complies for the first-order kinetics and accomplishes via a non-Fickian diffusion process. Moreover, the pot experiment demonstrates that the SC/SAH-SRF has higher growth promotion role for the maize seedlings than those of others. Consequently, this work provides a novel strategy for preparing environmentally friendly SRF by blending modified starch and hydrogel.

Effects of partial or full replacement of soybean meal with urea or coated urea on intake, performance, and plasma urea concentrations in lactating dairy cows.

We expected mitigation of the hypophagic effects of urea (U) with a coated urea (CU) product that aimed to partially shift urea supply to the post-ruminal gastrointestinal tract. Ruminal release and post-ruminal digestibility of CU was evaluated in vitro, followed by a randomised complete block experiment (54 Holstein-Friesian cows; 177 ± 72 days in milk). Soybean meal (SBM) was partially (PR) or fully (FR) replaced on an isonitrogenous basis by beet pulp and U or CU. Urea sources were included at 12 (U-PR, CU-PR) and 19 (U-FR, CU-FR) g/kg dietary dry matter (DM). Hypophagic effects were similar for U-PR and CU-PR (-11% vs. -7%), and for U-FR and CU-FR (-13% vs. -12%) compared with SBM (average 25.8 kg DM intake/d). Compared with SBM, U-PR and CU-PR reduced yields of milk (-8%) and protein (-12%), U-PR reduced yield of fat (-9%) and fat- and protein-corrected-milk (FPCM; -9%), and CU-PR tended to reduce FPCM yield (-5%). Compared with SBM, U-FR and CU-FR respectively reduced yields of milk (-21%, -22%), protein (-25%, -26%), fat (both -14%), lactose (-20%, -21%), and FPCM (-17%, -19%), and lowered N (-15%, -12%) and feed (-8%, trend, -9%) efficiency. Human-edible protein efficiency approximately doubled with U-PR and CU-PR and approximately tripled with U-FR and CU-FR compared with SBM. Milk composition and plasma urea concentration were similar between U and CU, except for a trend for a greater plasma urea concentration with U-PR compared with CU-PR. Dry matter intake patterns differed for CU-PR compared with U-PR and for CU-FR compared with U-FR, suggesting effects of urea release rate or location on feeding behaviour. Overall, replacing SBM with U or CU reduced DM intake and milk production and affected nutrient efficiencies. Coated urea influenced DM intake pattern but did not affect total DM intake or milk production compared with U.

Synthesis and characterization of chitosan-modified membrane for urea slow-release fertilizers

BackgroundUrea is a fertilizer widely used by farmers, especially vegetable farmers, due to its high nitrogen content, around 46 %. However, plants only use a small amount of nitrogen, a maximum of 35 %, while the remaining nitrogen is wasted and released into the environment. Undeniably, it causes increases production costs and environmental problems. A slow-release urea fertilizer (SRF) has been formulated to resolve these issues. MethodsIn this study, the membrane was made of chitosan with several crosslinking agents such as Tripolyphosphate (TPP). In addition, calcium ion bonds are expected to increase the interaction with urea fertilizer through the encapsulation process. The resultsOur data showed that urea slow-release fertilizer (SRF) with the chitosan/TPP/Ca membrane, was successfully synthesized. This membrane has the characteristics of a thin white layer that is transparent. The physical and chemical characterization of SRF membranes with various coating membrane variations showed that the chitosan/TPP/Ca-urea membrane has Young's modulus of 7.75–22.05 N/mm2, swelling of 109.52–132.62 % and porosity of 0.756–1.06 %. Functional group analysis shows that several spectral changes indicate the presence of crosslinking process between the chitosan functional groups and TPP. The urea release results show that the membrane is released through a diffusion mechanism. Furthermore, SEM results show that these membranes have pores with various shapes and sizes. ConclusionBased on the result, it can be concluded that chitosan membrane modification with the addition of TPP and calcium oxide provides improved membrane characteristic cs including degree of development, hydrophobicity, membrane stress, and nitrogen release on the membrane. This membrane shows is indicating suitability as a slow-release fertilizer.

Urea intercalated encapsulated microalgae composite hydrogels for slow-release fertilizers

In agriculture, hydrogels can be addressed for effective operation of water and controlled-release fertilizers. Hydrogels have a significant ability for retaining water and improving nutrient availability in soil, enhancing plant growth while reducing water and fertilizer usage. This work aimed to prepare a hydrogel composite based on microalgae and biopolymers including chitosan and starch for use as a soil conditioner. The hydrogel composite was characterized by FTIR, XRD, and SEM. All hydrogel properties were studied including swelling degree, biodegradability, water-holding capacity, water retention, and re-swelling capacity in soil and water. The urea fertilizer loading and releasing behavior of the prepared hydrogels were investigated. The results revealed that the range of the maximal urea loading was between 99 and 440%, and the kinetics of loading was fitted with Freundlich model. The urea release % exhibited 78–95%, after 30 days, and the kinetics of release was fitted with zero-order, Higuchi, and Korsmeyer–Peppas models. Furthermore, the prepared hydrogels obtained a significant water-holding capacity, after blending soil (50 g) with small amount of hydrogels (1 g), the capacity increased in the range of 99.4–101.5%. In sum, the prepared hydrogels have the potential to be applied as a soil conditioner.

Controlled release of urea using negatively charged polysaccharides

Controlled release of urea using negatively charged polysaccharides

Slow‐release fertilizer behavior of polyvinyl alcohol (PVA)/urea/TiO2 nanofiber membrane

AbstractNanofiber is a material used as a drug carrier matrix in drug release materials. Its morphology has high porosity and good flexibility, making it suitable for this purpose. The use of nanofiber as a carrier matrix in slow‐release fertilizer (SRF) material is expected to provide a solution for releasing fertilizer into the soil more measurably and efficiently In this study, PVA/Urea/TiO2 nanofibers were fabricated using the electrospinning method. PVA/Urea/TiO2 SRFs were prepared using varying urea mass percentages (10%, 15%, and 20% of PVA mass) and the concentration of titanium dioxide suspension solution (0, 0.2, and 0.4 mL). Every sample was analyzed using scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) and tested using contact angle and slow‐release tests. From SEM characterizations, all samples showed the ability to form nanofiber. It was found that the membrane diameter sizes for each sample A, B, C, D, E, and F were 341 ± 5, 309 ± 12, 109 ± 3, 313 ± 10, 109 ± 3, and 158 ± 6 nm, respectively. The FTIR characterizations showed that all the matrix samples successfully contained the nitrogen group, which was found at wave number 1605 cm−1 (NH deformation), 1574 cm−1 (CN stretching), and 3430 cm−1 (NH stretching). The SEM mapping images confirmed the presence of titanium dioxide (green dots). The contact angle test showed that all samples had hydrophilic properties (the contact angle value lower than 90°), and the greatest value of contact angle measurement was 31.08° for sample C/E (sample with the most presence of TiO2 suspension solution 0.4 mL). The sample with the greatest TiO2 suspension concentration (0.4 mL) had the longest urea release time, lasting 8 days. This result indicates the addition of TiO2, can potentially suppress the hydrophilic properties of the PVA membrane. It is found that the addition of TiO2 influenced the membrane's hydrophilicity, consequently increasing the release rate. This study used the Korsmeyer–Peppas mathematical kinetic model to show that diffusion and swelling are release mechanisms for SRF membranes.

Retention, Degradation, and Runoff of Plastic-Coated Fertilizer Capsules in Paddy Fields in Fukushima and Miyagi Prefectures, Japan: Consistency of Capsule Degradation Behavior and Variations in Carbon Weight and Stable Carbon Isotope Abundance

Paddy field runoff containing plastic capsules that are used to coat fertilizers has been receiving increased attention. However, the behavior of these capsules, especially their degradation behavior, has not been extensively investigated. We divided the capsules in runoff into two categories: “floating capsules after ploughing” and “floating capsules discharged via pipes at the exits of paddy fields”. The behaviors of the capsules in both types of runoff were monitored in 2022 and 2023 at four paddy fields in Fukushima and Miyagi prefectures in northern Japan. Sampling of capsules in paddy biomass and soil, and comparisons of capsule weight to biomass weight showed that a decrease in plastic capsule weight reflected a decrease in capsule runoff. However, the emergence of clear effects showed a delay of 2 to 3 years, as explained by carbon isotopic analyses. The decrease in the weight of the plastic capsules could be attributed to a combination of capsule degradation and the release of urea inside the capsules, which was also explained by carbon isotopic analyses. Three types of degraded capsules were found: shrunken, broken, and spherical. Statistically significant differences among the weights of each type found.

Valorization of lignin by crosslinking for slow-release urea fertilizer systems: A promising approach for agricultural applications

Slow-release fertilizers hold promise for their extensive use in agriculture. Urea, a commonly employed fertilizer, poses the risk of elevated nitrogen levels in soil due to its water solubility when used improperly. To address this issue, the development of a cost-effective and biodegradable urea slow-release matrix was pursued by crosslinking wheat straw-derived lignin with epichlorohydrin at varying ratios (1:1, 1:2, and 2:1) and subsequently impregnating it with urea. The crosslinked lignin matrices exhibited superior properties compared to unmodified lignin. After 8 days of immersion in water, the percentage release of urea from the crosslinked lignin matrices reached 48%, whereas it was 95% for unmodified lignin. Characterization techniques such as Fourier transform infrared spectroscopy, 13C nuclear magnetic resonance, and thermogravimetry analysis were employed to gain insights into the structural and functional aspects of the crosslinked lignin. The results revealed that the crosslinked lignin possessed a higher surface area and exhibited more suitable functional groups for urea impregnation. The controlled hydrophilic-lipophilic balance of the crosslinked lignin matrices offers significant advantages in fertilizer systems, enabling a controlled and gradual release of urea. This innovative approach not only offers enhanced control over nutrient delivery but also demonstrates the potential of lignin as a sustainable and cost-effective alternative for slow-release fertilizer formulations. This development provides an effective solution to address the issue of excessive nitrogen levels and opens up new avenues in material development, holds promise for sustainable agriculture and paves the way for further advancements in the field.

Preparation and characterization of slow-release urea fertilizer encapsulated by a blend of starch derivative and polyvinyl alcohol with desirable biodegradability and availability

In this study, a novel double-layer slow-release fertilizer (SRF) was developed utilizing stearic acid (SA) as a hydrophobic inner coating and a blend of starch phosphate carbamate (abbreviated as SPC) and polyvinyl alcohol (PVA) as a hydrophilic outer coating (designated as SPCP). The mass ratios of SPC and PVA in the SPCP matrices were systematically optimized by comprehensively checking the water absorbency, water contact angle (WCA), water retention property (WR), and mechanical properties such as percentage elongation at break and tensile strength with FTIR, XRD, EDS, and XPS techniques, etc. Moreover, the optimal SPCP/5:5 demonstrated superior water absorbency with an 80.2 % increase for the total mass compared to natural starch/PVA(NSP), along with desirable water retention capacity in the soil, exhibiting a weight loss of only 48 % over 13 d. Relative to pure urea and SA/NSPU/5:5, SA/SPCPU/5:5 released 50.3 % of its nutrient within 15 h, leading to nearly complete release over 25 h in the aqueous phase, while only 46.6 % of urea was released within 20 d in soil, extending to approximately 30 d. The slow release performance of urea reveals that the diffusion rate of urea release shows a significant decrease with an increase in coating layers. Consequently, this work demonstrated a prospective technology for the exploration of environmentally friendly SRF by integrating biodegradable starch derivatives with other polymers.

Hydrogel Nanocomposite Based Slow-Release Urea Fertilizer: Formulation, Structure, and Release Behavior

To enhance the nitrogen utilization efficiency of fertilizers, we developed a novel slow-release fertilizer hydrogel through free radical polymerization, incorporating lignin-containing cellulose nanofiber (LCNF), clinoptilolite (CL), urea, and acrylic acid (AA)-co-acrylamide (AAm) polymer. Various analytical techniques were utilized to examine the structure, swelling, and release behaviors of the fabricated hydrogels with varying LCNF concentrations. The results indicated that the addition of 10% LCNF led to a decrease in water absorption from 72.44 g g−1 to 24.04 g g−1. However, re-swelling was significantly enhanced, with a reduction in re-swelling capacity loss from 32.91% to 23.52%. Concurrently, water retention capacity notably increased from 18.03% to 39.20%. The hydrogel containing 10% LCNF exhibited a slower urea release over 30 days. The kinetic studies revealed that the swelling and urea release behaviors align well with the second-order kinetics model and the Peppas-Sahlin model, respectively. In summary, the developed LCNF/CL/(AA-co-AAm)/urea hydrogel nanocomposites present a novel strategy for the future production and utilization of slow-release fertilizers in agricultural and horticultural fields.

Polymer-coated urea applied at one-time mechanical topdressing increases nitrogen use efficiency and rice yield in the cold area

Context The application of slow and controlled release fertilisers can reduce nitrogen loss, but the research is still scarce in the cold rice region of China. Aims The study was conducted to screen slow-release or controlled-release fertilisers which can meet the nitrogen demand of rice and reduce NH3 volatilisation in different pH soils. Methods This experiment includes four fertilisation treatments: no fertiliser (control), urea, urea with N-(n-butyl) thiophosphorictriamide (NBPT), and polymer-coated urea (PCU). The amounts of urea-N, pH, ammonium-N (NH4+-N) in the surface water, and NH3 volatilisation were determined. Thereafter, to evaluate the effects of one-time mechanical topdressing of PCU mixed with compound fertilisers along with farmers’ fertilisation practice (FFP), field experiments carried out in wide soil pH differences were conducted. Key results Cumulative NH3 volatilisation was reduced in the NBPT treatment compared with the urea treatment. There was no significant difference between urea-N, NH4+-N, and pH in the surface water under PCU and control. NH3 volatilisation of PCU is negligible and significantly prolongs the soil nitrogen storage time. In the subsequent experiment, PCU blend increased yield, dry matter, nitrogen uptake, and the partial factor productivity of applied nitrogen (PFPN) compared to FFP. Conclusions PCU treatment slows down urea release and reduces ammonia volatilisation from paddy fields. In turn, it reduces ammonia-nitrogen levels and pH in surface water and further slows down the rate of ammonia volatilisation. Implications Application of PCU as a one-time mechanical topdressing fertiliser in rice fields in cold regions saves nitrogen fertiliser, increases crop yields, and reduces labour.

Preparation and Application of Degradable Lignin/Poly (Vinyl Alcohol) Polymers as Urea Slow-Release Coating Materials.

The massive amount of water-soluble urea used leads to nutrient loss and environmental pollution in both water and soil. The aim of this study was to develop a novel lignin-based slow-release envelope material that has essential nitrogen and sulfur elements for plants. After the amination reaction with a hydrolysate of yak hair keratin, the coating formulation was obtained by adding different loadings (2, 5, 8, 14 wt%) of aminated lignin (AL) to 5% polyvinyl alcohol (PVA) solution. These formulations were cast into films and characterized for their structure, thermal stability, and mechanical and physicochemical properties. The results showed that the PVA-AL (8%) formulation had good physical and chemical properties in terms of water absorption and mechanical properties, and it showed good degradation in soil with 51% weight loss after 45 days. It is suitable for use as a coating material for fertilizers. Through high-pressure spraying technology, enveloped urea particles with a PVA-AL (8%) solution were obtained, which showed good morphology and slow-release performance. Compared with urea, the highest urea release was only 96.4% after 30 days, conforming to Higuchi model, Ritger-Peppas model, and second-order dynamic model. The continuous nitrogen supply of PVA-AL coated urea to Brassica napus was verified by potting experiments. Therefore, the lignin-based composite can be used as a coating material to produce a new slow-release nitrogen fertilizer for sustainable crop production.

Synthesis of poly(ionic liquid-OH) mediated deacetylated chitin and its hydrogels: A study on their applications in controlled release of paracetamol and urea

Due to the biodegradable and biocompatible nature of chitin and chitosan, they are extensively used in the synthesis of hydrogels for various applications. In this work, deacetylation of chitin is carried out with alkaline poly(dimethyldiallylammonium-hydroxide) that gave a higher amount of water-soluble chitin (with 84 % of the degree of deacetylation = chitosan0.84) compared to deacetylation using NaOH. The water-soluble chitosan0.84 is used as intercalating chains for the preparation of acrylic acid and vinylimidazole-based hydrogels. The quaternization of imidazole groups is done with 1,ω-dibromoalkanes, which sets off the crosslinking in the above polymer network. A set of three chitosan0.84 intercalated hydrogels, namely Cs-C4-hydrogel, Cs-C5-hydrogel, and Cs-C10-hydrogel are prepared bearing butyl, pentyl, and decyl chains as respective crosslinkers. The swell ratios of these intercalated hydrogels are compared with those of non-intercalated hydrogels (C4-hydrogel, C5-hydrogel, and C10-hydrogel). Chitosan0.84 intercalated Cs-C10-hydrogel has excellent swelling properties (2330 % swelling ratio) among six synthesized hydrogels. SEM analysis reveals that decyl crosslinker-bearing hydrogels are highly porous. The multi-functionality of Cs-C10-hydrogel and C10-hydrogel is explored towards -the controlled release of paracetamol/urea, and methyleneblue dye absorption. These studies disclose that chitosan0.84 intercalated hydrogels are showing superior-swelling behavior, high paracetamol/urea loading capacities and better dye entrapment than their non-intercalated counterparts.