Increasing urea-N efficiency for transplanted lowland rice by pneumatic injection: Yield and economics at the farm level

To increase the fertilizer-N efficiency in lowland rice (Oryza sativa L.) cultivation, new management practices are needed. Main cause of the present low efficiency is the low N recovery by plants, as a considerable part of the N applied is lost; deep placement techniques improve the recovery. A pneumatic injector, with which urea prills can be point-placed at a depth of 5–10 cm in paddy soils, was tested in 38 on-farm trials in 1989/90, mostly during the wet season. The experiments, located in Africa and Asia, focussed on differences in grain yield between conventional methods of broadcasting urea and injection by the pneumatic injector, at recommended N-rates. The study shows that the pneumatic injector is effective as a tool to improve the N fertilizer efficiency. The average yield increases per region, resulting from the use of the injector, ranged from about 250 to 1300 kg grain ha^–1. The value of the yield increase would allow most farmers to recover the costs of the injector within one season, even if labour was hired to carry out the injections. The average labour requirement of the injector was 40 hours ha^–1. In Indonesia, injection of prilled urea gave yields similar to those obtained with urea briquettes.     

Factors controlling ammonia loss from trash covered sugarcane fields fertilized with urea

Ammonia losses following surface applications of urea to trash covered sugar cane fields were investigated in four climatic zones of tropical Queensland. Volatilization of ammonia and evaporation of water were determined by micrometeorological techniques. The results showed that the pattern, rate and extent of ammonia loss were controlled by the availability of water in the trash and its evaporation. Water added by dewfall, rainfall or condensation of evaporated soil moisture dissolved some of the urea and allowed it to be hydrolyzed to ammonia by the urease enzyme in the sugarcane residues; when the water evaporated, ammonia was lost to the atmosphere.In the dry climatic zone, where no rain or dew fell, water addition to the trash by condensation of evaporated soil moisture was not sufficient to dissolve much urea so very little ammonia was lost. In the cool and warm moist zones, small additions of water to the trash from dew, light rain and condensation maintained a slow but steady pattern of ammonia loss over a period of six weeks and resulted in losses of 32% and 39% of the applied nitrogen. At the site in the wet zone, heavy rainfall apparently washed the urea from the trash layer into the soil and limited ammonia loss to 17% of the applied nitrogen.Substitution of ammonium sulfate for urea reduced ammonia loss to less than 1.8% of the applied nitrogen.     

用含硼T641石墨炭源合成耐热性金刚石

介绍了含硼T641石墨炭源合成耐热性高、抗氧化性好与化学惰性强的金刚石及其性质。讨论了含硼金刚石高耐热性的形成及其氧化机理。指出了进一步提高质量、耐热性、抗氧化性与化学惰性金刚石的合成途径及方法。     

生产粒状NPK复合肥的改良美国TVA法

粒状 NPK复合肥美国 TVA法之改良系利用美国 TVA的连续式滚筒氨化粒化机 ,设计加装一特殊埋床式反应器进行一系列的化学反应 ,释出大量的化学反应热 ,融化及溶解部分固体原料 ,改变原料物化性能 ,提供各种有利的造粒条件 ,促使氨化粒化机内的各种原料在最少的水分下 ,紧密结成坚硬浑圆 ,易于流动、搬运、储存 ,不结块的颗粒状 NPK复合肥。台湾引进美国 30年经验所研发出来的 TVA改良法具有如下特色 :(1)建厂成本低 ;(2 )原料选用宽广灵活 ,以致原料成本低 ;(3)干燥成品耗用燃料少 ;(4 )回流比小 ,用电量少 ;(5 )颗粒强硬、耐水 ,养分缓释持久 ;(6 )可生产多种不同配方的复合肥 ;(7)配方更改容易、迅速 ,适合少量多批次之生产     

Anionic Clays as Potential Slow-Release Fertilizers: Nitrate Ion Exchange

Several nitrate containing anionic clays were synthesized at different temperatures and the kinetics of NO₃ ^– release were determined to test their suitability as slow-release N fertilizers. A sample (Mg:Al = 2:1) synthesized at 60°C with smaller particle size released 75, 86 and 100% of its NO₃ ^– in 1, 3 and 7 days, respectively when equilibrated with a simulated soil solution. On the other hand, the 175°C/2 hrs sample with larger particle size released 65, 77 and 84% of its nitrate in 1, 3 and 7 days, respectively. Another anionic clay (synthesized at 175°C/24 hrs) of higher charge density (Mg:Al = 2:1) containing NO₃ ^– was equilibrated with a 0.012 N NaCl or Na₂CO₃ to test the role of different anions in releasing the NO₃ ^– anion from the interlayers. The results showed that Cl^– released more NO₃ ^– than did CO₃ ^2– from this anionic clay after all the treatment times probably as a result of the CO₃ ^2– anion blocking the release of NO₃ ^– from the interior of the crystals. When a lower charge density (Mg:Al = 3:1) sample (synthesized at 175°C/48 hrs) was equilibrated with 0.02N solution of anions the release of nitrate was as follows: Cl^– < F^– < SO₄ ⁼ CO₃ ^2–. These results suggest that the divalent SO₄ ⁼ and CO₃ ^2– anions are more effective in the release of NO₃ ^– from this lower charge density anionic clay. Time-resolved structural analysis of NO₃ ^– exchange with CO₃ ^2– in the above anionic clay using synchrotron x-ray diffraction showed that ion exchange is rapid because of small crystal size and lower charge density. Thus the release of NO₃ ^– from anionic clays is an interplay among the type of anions present in soil solution, their concentration, pH of soil solution, the charge density and crystal size of anionic clay etc.     

B4C reinforced NiTi-based composites: Microstructure and wear performance

In this study, NiTi–x wt.% B₄C (x = 0, 2, and 4) composites were consolidated with spark plasma sintering method, and the effects of boron carbide reinforcement addition on the microstructure and wear behavior of samples were investigated. Identification of the constituent phases of samples by the X-ray diffraction method plus Rietveld analysis revealed that the stability of the martensite phase increased in the composite samples because of mismatch stresses between the NiTi matrix phase and the reinforcing particles, which increases the density of the dislocations and facilitates the diffusion process that subsequently leads to the formation of stable intermetallics. The results of hardness test indicated that the hardness value increased from 3.67 GPa for pure NiTi to 10.99 GPa for NiTi–4 wt.% B₄C. Results of wear test revealed that boron carbide reinforced composite specimens had higher wear resistance, whereas wear rate of NiTi sample was 3.6 × 10⁻³ mm³/N m, and it reached to .21 × 10⁻³ mm³/N m for NiTi–4 wt.% B₄C. Investigation of microstructure by scanning electron microscopy images and EDS analysis revealed that the wear mechanism in NiTi samples was abrasive and the addition of B₄C to NiTi changed the wear mechanisms from abrasive to a combination of oxidation, adhesive, and delamination mechanisms.     

Spark plasma sintering of boron nitride micron tubes reinforced boron carbide ceramics with excellent mechanical property

In this paper, the novel boron nitride micron tubes (BNMTs) were used to reinforce commercial boron carbide (B₄C) ceramics prepared via spark plasma sintering technology. The effects of the sintering parameters, sintering temperature, the holding time, and the BNMTs content on the microstructure and mechanical properties of B₄C/BNMTs composite ceramics were studied. The results indicated that adding a proper amount of BNMTs could inhibit the grain growth of B₄C and improve the fracture toughness of the B₄C/BNMTs composite ceramics. The prepared composite ceramic sample with 5 wt% BNMTs at 1850°C, 8 min and 30 MPa displayed the best mechanical properties. The relative density, hardness, fracture toughness, and bending strength of the samples were 99.7% ± .1%, 35.62 ± .43 GPa, 6.23 ± .2 MPa m^1/2, and 517 ± 7.8 MPa, respectively. Therein, the corresponding value of hardness, fracture toughness, and bending strength was increased by 10.3%, 43.59%, and 61.5%, respectively, than that of the B₄C/BNMTs composite ceramic without BNMTs. It was proved that the high interface binding energy and bridging effect between boron carbide and BNMTs were the toughening principle of BNMTs.     

Mechanical properties of B4C–CrB2 binary eutectic composites prepared by arc-melting

B₄C–CrB₂ composites were prepared by arc-melting using B₄C and CrB₂ powders as raw materials. The eutectic composition of B₄C–CrB₂ system was 30B₄C–70CrB₂ (mol%) with a labyrinth-like irregularly layered eutectic microstructure, composed of B₄C phase about 1–2 μm in thickness dispersing in CrB₂ matrix, much smaller than raw powders. The interface of the eutectic composite was well bonded, and there were edge dislocations at the interface to alleviate the interface mismatch. The eutectic temperature of B₄C–CrB₂ composites was approximately 2200 K. At the eutectic composition, the B₄C–CrB₂ composites showed the maximum Vickers hardness (24.6 GPa) and fracture toughness (4.3 MPa m^1/2) at room temperature.     

Kinetics and isotherm studies for the adsorption of boron from water using titanium dioxide

Boron is a necessary element for plants that are generally found in the ground and seawater, but it can also be poisonous in large doses. Contamination of water with boric acid or borate ions is a global concern. Due to the absence of the chemical charge that boron possesses, its removal is often difficult. To investigate boron's adsorption characteristics, kinetic, isotherm, and isothermal studies were performed. The adsorption of boron was shown to be a pH-dependent mechanism, with the best results at around pH 9.0. About 47% of the boron from a solution of 50 mg L⁻¹ was removed using 5 g titanium dioxide in 30 min. It was also demonstrated that boron adsorption kinetics increased with temperature, which is best described by the pseudo-second-order kinetic model (R² > 0.98) and also fits well with Elovich and pseudo-first-order models (R² > 0.94) at pH 9.0. Equilibrium was reached in about 40 min for all the samples. The film boundary layer diffusion step limits the rate. Experimental results correspond well to the Freundlich isotherm (R² = 0.95–0.99). Langmuir and Temkin's isotherms also fitted reasonably well (R² = 0.94–0.98). The Freundlich and Langmuir constants indicate favourable adsorption. The Gibbs free energy (ΔG) values increased negatively (from −11.47 to −15.63 kJ mol⁻¹) with increasing temperature, signifying a feasible and spontaneous process. The enthalpy change (ΔH) value of about 30.35 kJ mol⁻¹ indicated endothermic physical adsorption. The results indicate that titanium dioxide is an excellent and safe adsorbent for the removal of boron from water.     

Ultrafine-grained B6O–diamond composites with superb mechanical properties

We report here the high-pressure and high-temperature (HPHT) synthesis of well-sintered B₆O–diamond composites from B₆O and carbon black nanopowders. The carbon black was transformed into diamond nanograins at HPHT conditions, and simultaneously formed high-strength B₆O–diamond interfaces. The ultrafine B₆O and diamond nanograins and the high-strength B₆O–diamond interfaces synergistically construct excellent mechanical properties for the synthesized composites. The B₆O–diamond composites possess a hardness (avg. 52 GPa) comparable to that of polycrystalline diamond (40–60 GPa), whereas the fracture toughness (avg. 7.2 MPa m^1/2) is increased several times compared to previously synthesized polycrystalline B₆O ceramics (1.7–3.1 MPa m^1/2) and B₆O-based composites (3–4 MPa m^1/2). Fracture behavior analysis demonstrates that the main toughening mechanisms in this B₆O–diamond composite are nanotwin toughening, crack deflection, and crack bridging.