Preparation and properties of a slow release NP compound fertilizer with superabsorbent and moisture preservation

A slow‐release NP compound fertilizer with superabsorbent and moisture preservation was prepared by carboxyl methyl starch, acrylic acid, ammonia, urea, diammonium phosphate, and so on. The effects of the amount of initiator, crosslinker, and the degree of neutralization of acrylic acid on water absorbency were investigated and optimized. The product was characterized by FTIR, ICP, and element analysis, and the results showed that the product contained 22.6% nitrogen element and 7.2% phosphor (shown by P₂O₅) element. Its water absorbency was about 85 (g · g^?1) times its own weight in tap water. We also investigated the water retention property of the product and the slow release behavior of N and P in the product. The results showed that the product had a good water retention capacity and slow release property. The mechanism of the release of N and P in water was also investigated. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 2132–2138, 2005     

脲醛缓释肥料在水稻上的应用研究

对脲醛缓释肥料在水稻上的应用进行肥效试验。结果表明:施用脲醛缓释肥料可延长水稻生育期5~7 d;有效提高分蘖苗数、有效穗和株高,增加总粒数和实粒数,降低空秕率,提高千粒质量;增产增收效果明显,增产幅度达4.73%~10.22%,每667 m2增加纯收益21.52~86.62元。     

脲醛缓释肥在橡胶树上的肥效研究

通过试验研究了脲醛缓释肥、脲醛缓释肥加尿素及尿素等6个养分投入量相同的处理对橡胶树胶水产量的影响.试验结果表明,施用脲醛缓释肥,提高了橡胶树胶水产量,以肥料中掺混60％脲醛缓释肥和40％普通尿素一次性施用效果最好,既降低了施用脲醛缓释肥的成本,又节省了劳动力.     

重量法测定脲甲醛缓释肥料活性指数的研究

研究重量法测定脲甲醛缓释肥料的活性指数,对重量法和行业标准HG/T 4137—2010指定测定方法测定结果进行相关性研究。结果表明,两种方法的测定结果存在极显著正相关性,相关系数为0.996 6,两种方法测定值的绝对差值范围为-0.85%~0.56%。重量法具有简便、高效和准确的特点,可替代HG/T 4137—2010中脲甲醛缓释肥料活性指数测定方法。     

Preparation of superabsorbent polymer with slow‐release phosphate fertilizer

A superabsorbent polymer with slow‐release phosphate fertilizer was prepared by esterification of polyvinyl alcohol (PVA) and phosphoric acid (H₃PO₄), which was a slow‐release fertilizer at the same time. The product's water absorbency (WA) was about 480 times its own weight if it was allowed to swell in distilled water at room temperature for 24 h. WA under various conditions, such as varying the reaction time, the amount of sodium carbonate (Na₂CO₃), the reaction temperature, and the concentration of phosphoric acid ([H₃PO₄]), were investigated and optimized. The optimal sample of the product was characterized by FTIR and elemental analysis. The results showed that phosphoric groups had grafted on PVA molecule chains, and the content of P₂O₅ in the product was 31.2%. The water retention property and phosphate slow‐release mechanism of the product were studied as well. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 3417–3421, 2004     

Preparation of superabsorbent slow release nitrogen fertilizer by inverse suspension polymerization

A superabsorbent, slow release nitrogen fertilizer (SSRNF) was prepared by inverse suspension polymerization of partially neutralized acrylic acid using N,N′‐methylene bisacrylamide as a crosslinker and ammonium persulfate as an initiator in the presence of urea. The polymer was characterized using infrared spectral analysis, and network structural parameters such as molecular weight between crosslinks (M_c) and crosslink density (q) were calculated. The effects of reaction conditions, such as reaction time, reaction temperature, initiator, crosslinker and the degree of neutralization of acrylic acid, on water absorbency were investigated. The nitrogen content of SSRNF synthesized under optimal conditions was 22.7%, and the water absorbencies were about 965 g g^?1 in distilled water and 185 g g^?1 in tap water. The nitrogen slow release behaviors of the SSRNF in water and water retention capacity of soil with the SSRNF were also investigated. A possible slow release mechanism was proposed and the release rate constant K and the diffusion coefficient D of urea in the hydrogel was calculated. The results showed that the product not only had good slow release properties but also excellent soil moisture preservation capacity, which could effectively improve the utilization of fertilizer and water resources simultaneously. Therefore, the SSRNF is a multifunctional water managing material, which would find application in agriculture and horticulture, especially in drought‐prone areas where the availability of water is limited. Copyright © 2006 Society of Chemical Industry     

Evaluation of melamine‐modified urea‐formaldehyde resins as particleboard binders

Particleboards bonded with 6 and 12% melamine‐modified urea‐formaldehyde (UMF) resins were manufactured using two different press temperatures and press times and the mechanical properties, water resistance, and formaldehyde emission (FE) values of boards were measured in comparison to a typical urea‐formaldehyde (UF) resin as control. The formaldehyde/(urea + melamine) (F/(U + M)) mole ratio of UMF resins and F/U mole ratio of UF resins were 1.05, 1.15, and 1.25 that encompass the current industrial values near 1.15. UMF resins exhibited better physical properties, higher water resistance, and lower FE values of boards than UF resin control for all F/(U + M) mole ratios tested. Therefore, addition of melamine at these levels can provide lower FE and maintain the physical properties of boards. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Production of melamine fortified urea‐formaldehyde resins with low formaldehyde emission

Melamine can be incorporated in the synthesis of urea‐formaldehyde (UF) resins to improve performance in particleboards (PB), mostly in terms of hydrolysis resistance and formaldehyde emission. In this work, melamine‐fortified UF resins were synthesized using a strong acid process. The best step for melamine addition and the effect of the reaction pH on the resin characteristics and performance were evaluated. Results showed that melamine incorporation is more effective when added on the initial acidic stage. The condensation reaction pH has a significant effect on the synthesis process. A pH below 3.0 results on a very fast reaction that is difficult to control. On the other hand, with pH values above 5.0, the condensation reaction becomes excessively slow. PBs panels produced with resins synthesized with a condensation pH between 4.5 and 4.7 showed good overall performance, both in terms of internal bond strength and formaldehyde emissions. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Preparation and characterization of a superabsorbent slow‐release fertilizer with sodium alginate and biochar

A novel hydrogel was synthesized through the graft copolymerization of acrylic acid (AA) and acrylamide (AM) onto sodium alginate with ammonium persulfate as the initiator, methylene bisacrylamide as the crosslinking agent, and calcium chloride as the precipitating agent. Rapeseed meal biochar made at 300 °C was also used. A series of graft copolymers with various molar ratio of AA to AM was prepared. The structures of the hydrogels were characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. The free absorbency and rate of release were investigated. The grafting efficiency increased as the concentration of AM increased. There was a considerable percentage of nitrogen in the graft copolymers, and the release rate of nitrogen from fertilizer in soil and water decreased with increasing concentration of AM. The water retention of soil without hydrogel remained at 63 and 53.4% on the 10th and 20th days, but with the hydrogels, it was above 70% even on the last day. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45966.     

Uron and uron–urea‐formaldehyde resins

The favored pH ranges for the formation of urons in urea‐formaldehyde (UF) resins preparation were determined, these being at pH's higher than 6 and lower than 4 at which the equilibrium urons ↔ N,N′‐dimethylol ureas are shifted in favor of the cyclic uron species. Shifting the pH slowly during the preparation from one favorable range to the other causes shift in the equilibrium and formation of a majority of methylol ureas species, whereas a rapid change in pH does not cause this to any great extent. UF resins in which uron constituted as much as 60% of the resin were prepared and the procedure to maximize the proportion of uron present at the end of the reaction is described. Uron was found to be present in these resins also as linked by methylene bridges to urea and other urons and also as methylol urons, the reactivity of the methylol group of this latter having been shown to be much lower than that of the same group in methylol ureas. Thermomechanical analysis (TMA) tests and tests on wood particleboard prepared with uron resins to which relatively small proportions of urea were added at the end of the reaction were capable of gelling and yielding bonds of considerable strength. Equally, mixing a uron‐rich resin with a low F/U molar ratio UF resin yielded resins of greater strength than a simple UF of corresponding molar ratio indicating that UF resins of lower formaldehyde emission with still acceptable strength could be prepared with these resins. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 72: 277–289, 1999     

Synthesis and characterization of slow‐release nitrogen fertilizer with water absorbency: Based on poly(acrylic acid‐acrylic amide)/Na‐bentonite

A novel slow‐release nitrogen fertilizer with high‐water absorbency (SRNFWA) was prepared by cross‐linking poly (acrylic acid‐acrylic amide)/bentonite and urea. The synthesis conditions were studied systematically and optimized by using the response surface methodology (RSM). Meanwhile, the effects of the concentration of cross‐linker, initiator, bentonite, and degree of neutralization of acrylic acid on WA were investigated. The SRNFWA was characterized by Fourier transform infrared (FTIR) spectroscopy, elemental analysis, and scanning electron microscopy (SEM). The results of SEM showed the undulant and coarse surface, facilitated the permeation of nutrition into the polymeric network. We also investigated the slow release property and release mechanism of the nitrogen from the network structure, and the WA in different external solutions. The released characteristic of nitrogen was less than 15% by the third day and reached up to almost 75% after 30 days in distilled water. The WA was 700 g g^?1 and 150 g g^?1 in distilled water and 0.9 wt % NaCl solutions, respectively. These studies exhibited the excellent slow‐release property and WA capacity of this polymer in 0.9 wt % NaCl solution and could be quite effective in improving the utilization of fertilizer and its water retention capacity simultaneously. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

抑制剂生产长效复混（合）肥工艺技术

阐述在复混肥中加入抑制脲酶和(亚)硝化细菌活性的抑制剂,可控制铵态氮、硝态氮转化为N2O、N2造成的氮损失,从而提高氮利用率8%～12%,氮、磷、钾的综合利用率提高17%～25%。抑制剂加入量为复混肥量的1%～1.5%。介绍复混肥不同加工方法,如何加入抑制剂,并简单说明长效复混肥所增加的成本(18～20元/t产品)及带来的经济效益。     

Synthesis and characterization of chitosan/urea‐formaldehyde shell microcapsules containing dicyclopentadiene

Microcapsules containing healing agent have been used to develop the self‐healing composites. These microcapsules must possess special properties during the use of composites such as stability in surrounding, appropriate mechanical strength, and lower permeability. A new series of microcapsules containing dicyclopentadiene with chitosan/urea‐formaldehyde copolymer as shell materials were synthesized by in situ copolymerization technology. The microencapsulating mechanism was discussed and the process was explained. Also, the factors influencing the preparation of microcapsules were analyzed. The morphology and shell wall thickness of microcapsules were observed by using scanning electron microscopy. The size of microcapsules was measured using optical microscope and the size distribution was investigated based on data sets of at least 200 measurements. The chemical structure and thermal properties of microcapsules were characterized by Fourier transform infrared spectroscopy and thermogravimetric analysis, respectively. The storage stability and isothermal aging experiment of microcapsules were also investigated. Results indicted that the chitosan/urea‐formaldehyde microcapsules containing dicyclopentadiene were synthesized successfully; the copolymerization occurred between chitosan and urea‐formaldehyde prepolymer. The microcapsule size is in the range of 10–160 μm with an average of 45 μm. The shell thickness of microcapsules is in the range of 1–7 μm and the core content of microcapsules is 67%. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

A study on the colloidal nature of urea‐formaldehyde resins and its relation with adhesive performance

Urea‐formaldehyde (UF) resins present a swollen colloidal phase dispersed within a continuous water phase containing soluble oligomers. The main goal of the present investigation is to clarify the physical and chemical nature of those two phases and elucidate their impact on the bonding process. Optical and electronic microscopy has provided information on the morphology of the colloidal phase, showing primary particles and particle agglomerates. Mechanisms are suggested for the colloidal stabilization and dilution‐induced flocculation. Three commercial UF resins with different F/U molar ratios were studied using particle size distribution (PSD) analysis. The results showed the influence of the resin's degree of condensation and the aging status on the size of the colloidal structures. Gel permeation chromatography analysis was performed on samples of different resins and of the respective continuous and dispersed phases, separated by centrifugation. The quantified fraction of insoluble molecular aggregates present in the chromatograms was related to the resins synthesis conditions and age. Differential scanning calorimetry and tensile shear strength tests were performed to evaluate the reactivity and adhesive performance of each phase. It is suggested that the colloidal phase acts as a reactive filler at the wood joint interfaces, contributing for the resins bonding performance. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Mechanical properties of blends of HDPE and recycled urea‐formaldehyde resin

The mechanical properties of blends of high‐density polyethylene (HDPE) with a recycled thermosetting filler, urea‐formaldehyde grit (UFG), were evaluated in the range of 0–23% of filler by volume. Ethylene‐acrylic acid (EAA) copolymers and an ionomer based on EAA were evaluated as compatibilizers. The observed tensile modulus of the ionomer‐treated blends was raised to three times the modulus of virgin polyethylene, whereas the modulus of the untreated blends reached double that of polyethylene. The ionomer‐treated blends also showed a higher tensile strength than the blends without filler treatment. The improvement in the properties was assigned to an increased interaction between the filler and the polymer matrix. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 77: 3220–3227, 2000     

Curing of low level melamine‐modified urea‐formaldehyde particleboard binder resins studied with dynamic mechanical analysis (DMA)

Effects of resin formulation, catalyst, and curing temperature were studied for particleboard binder‐type urea‐formaldehyde (UF) and 6 ～ 12% melamine‐modified urea‐melamine‐formaldehyde (UMF) resins using the dynamic mechanical analysis method at 125 ～ 160°C. In general, the UF and UMF resins gelled and, after a relatively long low modulus period, rapidly vitrified. The gel times shortened as the catalyst level and resin mix time increased. The cure slope of the vitrification stage decreased as the catalyst mix time increased, perhaps because of the deleterious effects of polymer advancements incurred before curing. For UMF resins, the higher extent of polymerization effected for UF base resin in resin synthesis increased the cure slope of vitrification. The cure times taken to reach the vitrification were longer for UMF resins than UF resins and increased with increased melamine levels. The thermal stability and rigidity of cured UMF resins were higher than those of UF resins and also higher for resins with higher melamine levels, to indicate the possibility of bonding particleboard with improved bond strength and lower formaldehyde emission. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 377–389, 2005     

13C‐NMR study on the structure of phenol‐urea‐formaldehyde resins prepared by methylolureas and phenol

Phenol‐urea‐formaldehyde (PUF) resins were synthesized by reacting mixture of methylolureas (MMU), phenol, and formaldehyde. The structure of PUF cocondensed resins at different stages of reaction were analyzed by liquid ¹³C nuclear magnetic resonance (NMR) spectroscopy. The liquid ¹³C‐NMR analysis indicated that methylolureas had the dominant content in MMU with the reaction between urea and formaldehyde under the alkaline condition. The PUF cocondensed resins had no free formaldehyde. methylolureas were well incorporated into the cocondensed resins by reacting with phenolic units to form cocondensed methylene bridges. The second formaldehyde influenced the further reaction and the structure of the PUF resins. The resins with the prepared method of PUFB possessed relatively high degree of polymerization and low proportion of unreacted methylol groups. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Utilization of plant ash for the fabrication of novel superabsorbent composites with potassium‐release characteristics

Design and synthesis of the agricultural and ecological superabsorbent materials with cost‐efficient and fertilizer‐release characteristics has recently attracted considerable interests. In this work, the novel poly(sodium‐potassium acrylate‐co‐acrylamide)/plant ash (PNa‐KA‐co‐AM/PA) superabsorbent composites with potassium‐release characteristics were prepared using partially neutralized acrylic acid (Na‐KA), acrylamide (AM), and plant ash (PA) as raw materials, ammonium persulfate (APS) as the initiator, and N,N′‐methylenebisacrylamide (MBA) as the crosslinker. The structure, morphologies, and thermal stability of the composites were characterized by Fourier transform infrared spectrophotometer, scanning electron microscopy, and TGA techniques, respectively. The effects of MBA concentration and PA content on water absorbency were studied, and the swelling properties of the composites in saline solutions and various pHs solution as well as their potassium‐release capabilities were also evaluated. Results indicate that the composites exhibit better thermal stability, salt‐resistant performance, pH‐stability, and potassium‐release properties, and can act as a fertilizer and an effective water‐saving material for agricultural and ecological application. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

可生物降解PBAT包膜尿素缓释肥料的制备与性能研究

以可生物降解PBAT为包膜材料,通过循环流化床工艺制备一系列PBAT包膜尿素缓释肥料,并对制备工艺进行了优化;通过扫描电镜观察包膜肥料表面形态特征,分析缺陷形成原因;通过水中静置法测试PBAT包膜尿素缓释肥料的缓释性能,测定缓释曲线,样品的初期释放率为20%~50%,第28天的累积释放率为70%~90%。     

努力发展结合国情的缓(控)释肥料

通过对我国化肥工业的发展及新时期国民经济对化肥领域提出的综合要求,论述加速发展结合国情之缓释肥料的重要性。介绍了尿醛肥、稀土缓释肥、涂硫尿素和缓释掺混肥等品种的技术评述和可行性。