Application strategies for Sechura phosphate rock use on permanent pasture

At two phosphate (P) responsive sites in hill country the effectiveness of Sechura phosphate rock (SPR) as a direct application P fertilizer for permanent pasture was evaluated. Sechura was applied at two rates, in three different application strategies. The treatments were 16.7 and 50 kgP ha^–1 annually, 25 and 75 kgP ha^–1 biennially, and 50 and 150 kgP ha^–1 triennially giving a total of 50 and 150 kgP ha^–1, respectively, over three years. Single superphosphate (SSP) served as the standard P fertilizer. A comparison was also made between SPR and Chatham Rise phosphorite (CRP), another reactive PR. Total pasture and legume production and P uptake by pasture was measured with all fertilizer treatments over a three year period.In the year of application, SPR was as effective as SSP in stimulating total pasture and legume production and P uptake by pasture. This reflects the very reactive nature of this PR. In the second and third years of measurement, SPR did not show superior residual efffects to SSP. The ability of CRP to stimulate legume growth more than SPR in the second year following application demonstrates the danger of generalizing about the residual effects of reactive PR materials. Of the application strategies evaluated, a biennial appplication of 25 kgP ha^–1 as SPR maintained legume growth at a higher level than a smaller (16.7 kgP ha^–1) annual dressing. The biennial strategy also increased total pasture yield, in addition to legume production to a greater extent in the second and third years than a single (50 kgP ha^–1) triennial application.     

利用钛白废酸制高纯度磷酸一铵试验简介

试验表明,用钛白粉生产中副产的w(H2SO4)≈20%的钛白废酸,经浓缩、净化及再稀释后与磷矿粉反应,在加入净化添加剂的条件下制得纯净的湿法磷酸与氨或碳酸氢铵反应,可代替热法磷酸为原料生产相同质量的高纯度磷酸一铵。分析了该工艺的技术可行性和经济可行性,认为所得的纯净磷酸也可加工成其他高纯度磷化工产品。     

选磷厂废水电化学处理循环利用

简要介绍磷矿浮选厂废水（尾矿水）进行电化学处理的研究和处理后循环使用的浮选工艺试验以及含固废水电化学处理的理论基础。试验结果表明：经电化学处理后的废水达到工艺用水水质控制指标；反复循环使用于浮选工艺取得满意效果；电化学处理方法是实现工业废水循环利用的有效手段。     

大块液膜技术处理含六价铬废水

以磷酸三丁酯(TBP)为载体,煤油为稀释剂,NaOH为反萃剂,采用大块液膜技术处理含95~100mg/LCr(VI)的模拟废水。考察了液膜相用量、载体体积分数及反萃剂浓度对大块液膜过程中Cr(VI)传质过程的影响。结果表明,大块液膜技术对废水中Cr(VI)的去除效果较好。Cr(VI)迁移速率随TBP体积分数的提高而加快。当反萃剂NaOH浓度大于0.5mol/L时,反萃剂浓度对Cr(VI)传质过程的影响较小。处理后废水中Cr(VI)含量降至0.5mg/L以下,达到国家排放标准。     

Fate of nitrogen fertilizer applied to lowland rice on a Sulfic Tropaquept

A field experiment was conducted on an acid sulfate soil in Thailand to determine the effect of N fertilization practices on the fate of fertilizer-N and yield of lowland rice (Oryza sativa L.). A delayed broadcast application of ammonium phosphate sulfate (16-20-0) or urea was compared with basal incorporation of urea, deep placement of urea as urea supergranules (USG), and amendment of urea with a urease inhibitor. Deep placement of urea as USG significantly reduced floodwater urea- and ammoniacal-N concentrations following N application but did not reduce N loss, as determined from an¹⁵N balance, in this experiment where runoff loss was prevented. The urease inhibitor, phenyl phosphorodiamidate (PPD), had little effect on floodwater urea- and ammoniacal-N, and it did not reduce N loss. The floodwater pH never exceeded 4.5 in the 7 days following the first N applications, and application of 16-20-0 reduced floodwater pH by 0.1 to 0.3 units below the no-N control. The low floodwater pH indicated that ammonia volatilization was unimportant for all the N fertilization practices. Floodwater ammoniacal-N concentrations following application of urea or 16-20-0 were greater on this Sulfic Tropaquept than on an Andaqueptic Haplaquoll with near neutral pH and alkaline floodwater. The prolonged, high floodwater N concentrations on this Sulfic Tropaquept suggested that runoff loss of applied N might be a potentially serious problem when heavy rainfall or poor water control follow N fertilization. The unaccounted-for¹⁵N in the¹⁵N balances, which presumably represented gaseous N losses, ranged from 20 to 26% of the applied N and was unaffected by urea fertilization practice. Grain yield and N uptake were significantly increased with applied N, but grain yield was not significantly affected by urea fertilization practice. Yield was significantly lower (P = 0.05) for 16-20-0 than for urea; however, this difference in yield might be due to later application of P and hence delayed availability of P in the 16-20-0 treatment.     

Wettability and surfactivity of sodium phosphate surfactants in strong alkali solutions

The wettability, surfactivity and the correlation between wettability and surfactivity of sodium diethylhexylphosphate, sodium diethylhexyl polyoxyethylene phosphate and their complex in NaOH solutions were studied. A complex alkali resistant phosphate surfactant with good permeability was prepared. The wettability of surfactants was investigated by measuring the immersion time, sinking time and capillary effects of nature cotton grey fabric in NaOH solutions. The surfactivity of the surfactants was characterized by measuring the surface tension. The effect of the complex on the surface appearance of cotton grey fabric was also investigated with a scanning electron microscope (SEM). The results show that all the surfactants exhibit good wettability for cotton grey fabric in 0.5–5.0 mol/L of NaOH solutions, the complex system exhibits better wettability in 5.0–7.0 mol/L of NaOH solutions, in comparison with either corresponding single surfactant component employed, and wettability is well correlative with the surfactivities of the surfactant. SEM images indicate that the cotton grey fabric is well wetted by the alkaline surfactant solution and the quality of fabric is improved.     

Nanobubble generation and its applications in froth flotation (part Ⅲ): specially designed laboratory scale column flotation of phosphate

Froth flotation is used widely for upgrading raw phosphate. The flotation recovery of coarse phosphate (-1.18+0.425 mm) is much lower than that achieved on the -0.425+0.15 mm size fraction. Enhanced recovery of coarse phosphate particles is of great economic and environmental importance for phosphate industry. In this investigation, four different phosphate samples were aquired, characterized and tested in a specially designed laboratory-scale flotation column. Significant recovery improvement of coarse phosphate flotation was achieved using cavitation-generated nanobubble though its effects differ among the four testing phosphate samples. The laboratory-scale flotation column test results indicate that nanobubble increased P2O5 recovery by up to 10%-30% for a given Acid Insoluble (A.I.) rejection, depending on the characteristic of phosphate samples. The improvement ef-fect of nanobubble on the hard-to-float particles was more significant than that on easy-to-float particles, especially at lower col-lector dosages. Nanobubbles reduced the collector dosage by 1/3 to 1/2. Nanobubbles almost doubled the coarse phosphate flotation rate constant and increased the flotation selectivity index by up to 25%.     

Alkaline treatment kinetics of calcium phosphate by piezoelectric quartz crystal impedance

Calcium phosphate film was prepared by electrochemical deposition technology. Subsequently, the alkaline treatment process of calcium phosphate film in 0.1 mol/L NaOH solution was monitored on real time by the piezoelectric quartz crystal impedance (PQCI) technique. The variations of morphology and composition for the alkaline treatment products were characterized by scanning electron microscopy (SEM), Fourier transform infrared (FT-IR) and X-ray diffraction (XRD), respectively. The dynamic variations of calcium phosphate can be characterized by the change of equivalent circuit parameters. The results show that the forming process of hydroxyapatite (HA) is composed of three stages: (1) acidic calcium phosphate dissolution; (2) phase transformation; and (3) HA formation. Furthermore, the correlative kinetic equations and parameters are obtained by fitting the static capacitance (C _s)—time curves. Foundation item: Project(2005CB623901) supported by the Major State Basic Research and Development Program of China     

Mg2+掺杂的LiFePO4材料的共沉淀合成与表征

提出了一种采用共沉淀法合成镁掺杂的锂离子正极材料LiFePO4的新方法,研究了合成条件,采用XRD,SEM,循环伏安测定,电化学阻抗谱分析,以及充放电测试对合成的材料作了表征分析．结果表明,采用共沉淀合成方法可以获得性能良好的LiFePO4;Mg^2＋掺杂对LiFePO4结构没有产生明显的影响,但掺杂量的大小对LiFePO4的放电性能有较大影响．     

掺Er^3＋镓磷酸盐玻璃的光学性质

利用熔融淬火法制备了摩尔分数为40．8Ga2O3-58．0NaPO3-1．2Er2O3掺Er^3＋镓磷酸盐玻璃,测试并研究了样品中Er^3＋的吸收光谱、1．5μm发射光谱,根据Judd-Ofelt理论计算了Er^3＋离子强度参量Ωt（t=2,4,6）及自发辐射概率、荧光分支比、自发辐射寿命．结果表明,Er3＋1．5μm发射光谱半峰全宽达到40nm．同时,利用McCumber方法计算了Er^3＋4 I13／2→^4I15／2跃迁的受激发射截面,峰值达到6．10×10^-21cm^2,测定了Er^3＋4I13／2能级荧光寿命为4．88ms,^4I13／2能级量子效率为56．3％．