Effects of Regulation of C/N Ratio Wheat Straw Application on Nitrogen,Phosphorus and Potassium Uptake in Tobacco

[Objective]The aim was to study the effects of regulation of C/N ratio wheat straw application on tobacco nitrogen,phosphorus and potassium uptake. [Method]Effects of regulation C/N ratio wheat straw application on the flue-cured tobacco yield,output value,nitrogen,phosphorus and potassium content and cumulative uptake of the upper,middle and bottom leaf were studied by using the field plot experiments at Banqiao town,Qujing city,Yunnan Province during the 2008-2009 summer growing seasons. [Result]The results showed that the application of wheat straw alone or after C/N regulation,could significantly increase tobacco production,potassium content,the potassium and nitrogen accumulation amount of leaf,and was more conducive to the potassium uptake of tobacco leaf with wheat straw application after C/N regulation. Compared with non-straw application,the yield of tobacco increased by 6.59%,3.58%,5.98%,8.80% with application of wheat straw alone,wheat straw and vetch,wheat straw and oilseed cake,wheat straw and urea nitrogen,the potassium content in tobacco leaf increased by 3.85%,7.76%,8.82%,11.21%,respectively,the total potassium cumulative amount of leaf increased by 10.71%,11.62%,15.32% ,21.01% and the total nitrogen cumulative amount increased by 9.76%,1.22%,8.14%,14.00%. However,the differences of tobacco leaf nitrogen content among the different treatments were not significant,the phosphorus uptake of tobacco leaf decreased. [Conclusion]application of high C/N ratio wheat straw in flue-cured tobacco production,which should be concerned not only to adjust C/N ratio by adding nitrogen,but also considering additional phosphorus application.

基于高磷铁矿制备Fe-P合金催化剂用于高效全解水反应

本工作首次报道了一种高磷铁矿协同纯Ca_(3)(PO_(4))_(2)熔融还原并结合单辊旋淬技术制备Fe-P合金带材催化剂的短流程冶金工艺,该工艺具有成本低、产品附加值高、易于工业化的优点。针对电催化析氢合金催化剂低成本高效制备难题,国内外学者进行了重点研究。因此,通过短流程冶金的方法制备Fe-P合金带材催化剂并将其用于电催化制氢(HER)领域,一方面降低了冶金过程中二氧化碳和其他大气污染物的排放,另一方面为冶金资源实现“大型化、清洁化、连续化、自动化”再利用平台搭建提供了指导方案,有望解决催化剂技术在发展中存在的“卡脖子”问题。

热处理和泡沫铁对A356-SiC_(p)/Fe干滑动摩擦学性能的影响

采用真空辅助熔渗工艺制备泡沫铁骨架作为增强SiC_(p)/A359复合材料A359-SiC_(p)/Fe,对比进行泡沫铁增强前后和T6热处理前后,两种材料的显微硬度和高温磨损性能,明确泡沫铁和T6热处理对A359-SiC_(p)/Fe复合材料高温磨损性能增强的效果,并结合使用SEM与EDS对表面磨损形貌、磨屑形貌的观察表征,以探究该材料在不同温度下的高温磨损机理。结果表示,使用真空辅助熔渗工艺制备A359-SiC_(p)/Fe, Al-Fe界面结合良好,不仅形成了机械结合,还形成了化学冶金结合(靠近铝基体界面的相为Al_(12)Fe_(5)Si_(3);靠近泡沫铁基体处为Fe_(2)Al_(5)相;远离泡沫铁组织,呈游离状态的合金相为Al_(4)FeSi)。A359-SiC_(p)/Fe在300~500℃的磨损量仅为未增强合金的25%~75%,有效将高温环境下的使用温度提升50~100℃以上。T6热处理能够明显提高Al基体的硬度以及Al-Fe界面的冶金结合程度,且在300~500℃时效果更明显,有效提高材料的高温耐磨性能。材料的磨削形式受温度影响,100℃时为磨粒磨损,摩擦温度到达350℃时表面出现分层和剥落,500℃时,开始粘着磨损。

利用Fe-P-N-H_(2)O体系E-pH图对硝磷酸体系合成磷酸铁的热力学分析研究

硝磷酸法合成磷酸铁新工艺因生产流程简单、磷源成本低、设备投资小、能耗较低、绿色环保而具有很强的竞争力。利用FactSage和HSC等热力学软件中已有的热力学数据并运用E-pH图的绘制原理,得到Fe-P-N-H_(2)O体系不同浓度、298~473 K的E-pH关系图。研究表明,在水溶液中,磷酸铁具有较大的热力学稳定区域,能够很好地解释现有的液相沉淀法制备磷酸铁的实际操作条件。此外,从E-pH图中获得了共沉淀法合成磷酸铁的合适条件:温度为363 K左右、高氧化还原电位为0.5 V、适宜pH为1~3、浓度为0.01 mol/L,该工艺为硝磷酸体系共沉淀法合成磷酸铁提供了热力学理论依据。

BCC Fe中P晶界偏析对拉伸变形行为影响的分子动力学研究

晶界是金属材料中重要的微观结构,并且晶界上的位错形核对材料变形起着至关重要的作用。本文通过分子动力学模拟研究了BCC Fe中对称倾侧晶界的位错形核机制和孪晶机制,分析了P的晶界偏析对位错变形行为的影响机理。对于(111)晶界体系,位错形核扩展主导拉伸变形行为。而对于(112)孪晶界体系,拉伸变形主要是由孪晶主导,体系发生BCC-FCC相变。针对5个对称倾侧晶界(旋转角为30°~160°)体系,在不同温度下(300 K和600 K)施加拉伸载荷,结果表明位错形核受晶界类型和温度影响。与300 K相比,600 K下体系强度降低,促进位错形核。同时,从原子微观结构、体系能量两个角度,研究P的晶界偏析对位错形核的影响机理。本文提供了晶界位错形核的原子机制,有助于理解P在BCC Fe中的偏析对晶界变形行为和力学性能的影响。

Effects of ambient DIN:DIP ratio on the nitrogen uptake of harmful dinoflagellate Prorocentrum minimum and Prorocentrum donghaiense in turbidistat

The effects of varying nitrogen （N）： phosphorus （P） ratios on the growth and N-uptake and assimilation of the harmful dinoflagellates Prorocentrum minimum and Prorocentrum donghaiense were examined in turbidistat culture experiments. Algal cultures were supplied with media containing PO4^3- in various concentrations to obtain a wide range of N：P ratios. Experiments to determine rates of N uptake and assimilation of different N sources （NO^3-, NH4^＋, urea and glycine by P. minimum and NO3^-, NH4^＋ by P. donghaiense） were conducted using ^15-N tracer techniques at each N：P ratio. The growth rates suggested nutrient limitation at both high and low N：P ratios relative to the Redfield ratio. On a diel basis, the growth of both species was regulated by the light-dark cycle, which may be a result of regulation of both lightdependent growth and light-independent nutrient uptake. Maximum growth rates of both species always occurred at the beginning of light phase. In P-rich medium （low N：P ratio）, both species had higher N assimilation rates, suggesting N limitation. Low assimilation coefficients at high N：P ratios suggested P limitation of N uptake and assimilation. NO3 ^-and NH4^＋ contributed more than 90% of the total N uptake of P. minimum. Reduced N sources were more quickly assimilated than NO3^-. Highest average daily growth rates were recorded near an N：P ratio of 12 for both species. The N uptake rates of cultures at N：P ratios near Redfield ratio were more balanced with growth rates. The linkage between growth rates and N uptake/assimilation rates were conceptually described by the variation of cell N quota. The N：P ratios affect the N uptake and growth of Prorocentrum spp., and may regulate their bloom progression in eutrophic ecosystems.

Effects of COD to Phosphorus Ratios on the Metabolism of PAOs in Enhanced Biological Phosphorus Removal with Different Carbon Sources

To elucidate the phosphorus removal and metabolism under various COD / P ratio,a sludge highly enriched in PAOs was used to investigate the impacts of COD / P in batch tests under different carbon supply conditions. Acetate,propionate and a mixture of acetate and propionate at a ratio of 3 ∶ 1( COD basis) was used as carbon sources with the COD / P of 20,15,10 and 5. 0 g COD /gP,respectively. The minimum COD / P ratios for complete P removal were found to be 8. 24 g COD /gP for acetate,11. 40 g COD /gP for propionate and9. 10 g COD /gP for the 3 ∶ 1 mixture of acetate and propionate. Converted to a mass basis,all three cases had a very similar ratio of 7. 7 g VFA /gP,which represented a useful guide for operation of EBPR plants to identify possible shortages in VFAs. The trend in PHV accumulation during the anaerobic period along with the decrease of COD / P ratios suggested that,PAOs may use the TCA pathway for anaerobic VFA uptake to maintain the required NADH production with reduced glycogen degradation. During the aerobic phase,the glycogen pool was reduced but remained enough compared to the requirement for anaerobic VFA uptake,and the synthesis and degradation of glycogen was not the inhibition factor of PAOs.

Two stages of immiscible liquid separation in the formation of Panzhihua-type Fe-Ti-V oxide deposits,SW China

Magmatic oxide deposits in the～260 Ma Emeishan Large Igneous Province（ELIP）,SW China and northern Vietnam,are important sources of Fe,Ti and V.Some giant magmatic Fe-Ti-V oxide deposits, such as the Panzhihua,Hongge,and Baima deposits,are well described in the literature and are hosted in layered mafic-ultramafic intrusions in the Panxi region,the central ELIP.The same type of ELIP- related deposits also occur far to the south and include the Anyi deposit,about 130 km south of Panzhihua,and the Mianhuadi deposit in the Red River fault zone.The Anyi deposit is relatively small but is similarly hosted in a layered mafic intrusion.The Mianhuadi deposit has a zircon U-Pb age of～260 Ma and is thus contemporaneous with the ELIP.This deposit was variably metamorphosed during the Indosinian orogeny and Red River faulting.Compositionally,magnetite of the Mianhuadi deposit contains smaller amounts of Ti and V than that of the other deposits,possibly attributable to the later metamorphism.The distribution of the oxide ore deposits is not related to the domal structure of the ELIP.One major feature of all the oxide deposits in the ELIP is the spatial association of oxide-bearing gabbroic intrusions,syenitic plutons and high-Ti flood basalts.Thus,we propose that magmas from a mantle plume were emplaced into a shallow magma chamber where they were evolved into a field of liquid immiscibility to form two silicate liquids,one with an extremely Fe-Ti-rich gabbroic composition and the other syenitic.An immiscible Fe-Ti-（P） oxide melt may then separate from the mafic magmas to form oxide deposits.The parental magmas from which these deposits formed were likely Fe-Ti-rich picritic in composition and were derived from enriched asthenospheric mantle at a greater depth than the magmas that produced sulfide-bearing intrusions of the ELIP.

Efficient removal of Al(Ⅲ)and P507 from high concentration MgCl_(2)solution based on in-situ reaction strategy

For a highly efficient recycling of a wastewater containing a high concentration of MgCl_(2),Al(Ⅲ)and P507 were scheduled to be removed in advance.In this study,the in-situ removal of Al(Ⅲ)and P507 from a high concentration MgCl_(2)solution at different pH values and Al/P molar ratios was investigated.The results showed that P507 formed organic complexes of Al_(x)(OH)_y^(Z+)-P507 at pH of 2.0-4.0.At pH of 4.0-5.0,Al(Ⅲ)precipitated and transferred into Al(OH)_(3)with a flocculent amorphous morphology.Active sites on the Al(OH)_(3)surface enhanced the removal efficiency of P507.At pH of 6.0-6.5,Al(Ⅲ)and Mg(Ⅱ)formed layered crystalline Al(OH)_(3)and MgAl_(2)(OH)_(8with)small pore channels and fewer active sites,resulting in a reduced removal efficiency of P507.When the Al/P molar ratio exceeded 13 and the pH was between 4.0 and 5.0,the removal rates of both Al(Ⅲ)and P507 were higher than98%,while the concentration loss of Mg(Ⅱ)was only 0.2%-0.9%.

Effects of Co-Existing Ions on the Phosphorus Potassium Ratio of the Precipitate Formed in the Potassium Phosphate Crystallization Process

Livestock wastewater is mainly treated with activated sludge, but ions such as phosphorus, potassium, ammonium, nitrate and sulfate remain in the effluent. In this study, the effects of residual ions on phosphorus recovery using the magnesium potassium phosphate crystallization method were investigated when magnesium was added to increase the pH. If co-existing ions affect the products, the phosphorus to potassium molar ratio (K/P ratio) of the precipitate will deviate from being equimolar. Artificial wastewater test solutions containing 5.6 - 20.3 mM ammonium, 25.6 mM potassium, 6.5 mM phosphorus, 0 - 7.35 mM nitrate, and 0 - 3.06 mM sulfate were used. First, the optimum operating pH and amount of magnesium added to give a high phosphorus removal rate and recovery rate were determined. The experimental setup was a 10 L aerated and stirred reactor, and a 5 L settling tank. The K/P ratio in precipitate was approximately 1 using the optimum conditions. Continuous 2 h treatment allowed a white precipitate containing about 30 g of needle-like crystals to be obtained. Next, the effects of varying the ammonium, nitrate, and sulfate ion concentrations in the artificial effluent were investigated. Ammonium and sulfate ion concentrations of 8 mM or more and 3 mM or more, respectively, caused the K/P ratio to decrease to about 0.7 and 0.5, respectively. Varying the nitrate concentration did not affect the K/P ratio, even at a nitrate concentration of 7.35 mM.

Effect of nitrogen and phosphorus addition on leaf nutrient concentrations and nutrient resorption efficiency of two dominant alpine grass species

Nitrogen(N)and phosphorus(P)are two essential nutrients that determine plant growth and many nutrient cycling processes.Increasing N and P deposition is an important driver of ecosystem changes.However,in contrast to numerous studies about the impacts of nutrient addition on forests and temperate grasslands,how plant foliar stoichiometry and nutrient resorption respond to N and P addition in alpine grasslands is poorly understood.Therefore,we conducted an N and P addition experiment(involving control,N addition,P addition,and N+P addition)in an alpine grassland on Kunlun Mountains(Xinjiang Uygur Autonomous Region,China)in 2016 and 2017 to investigate the changes in leaf nutrient concentrations(i.e.,leaf N,Leaf P,and leaf N:P ratio)and nutrient resorption efficiency of Seriphidium rhodanthum and Stipa capillata,which are dominant species in this grassland.Results showed that N addition has significant effects on soil inorganic N(NO_(3)^(-)-N and NH_(4)^(+)-N)and leaf N of both species in the study periods.Compared with green leaves,leaf nutrient concentrations and nutrient resorption efficiency in senesced leaves of S.rhodanthum was more sensitive to N addition,whereas N addition influenced leaf N and leaf N:P ratio in green and senesced leaves of S.capillata.N addition did not influence N resorption efficiency of the two species.P addition and N+P addition significantly improved leaf P and had a negative effect on P resorption efficiency of the two species in the study period.These influences on plants can be explained by increasing P availability.The present results illustrated that the two species are more sensitive to P addition than N addition,which implies that P is the major limiting factor in the studied alpine grassland ecosystem.In addition,an interactive effect of N+P addition was only discernable with respect to soil availability,but did not affect plants.Therefore,exploring how nutrient characteristics and resorption response to N and P addition in the alpine grassland is important to understand nutrient use strategy of plants in terrestrial ecosystems.

Role of Fe/S ratios in the enhancement of uranium bioleaching from a complex uranium ore by Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans consortium

The role of Fe/S ratios(ω, g/g) in the uranium bioleaching from a complex uranium ore by Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans consortium was investigated. The results showed good uranium extraction with over 90% at the Fe/S ratio of 5:0.5, 5:1 and 5:5, while poor extraction(<46%) at the Fe/S ratio of 5:0 and 5:10.Furthermore, the bacterial community analysis based on species-specific gyrB numbers indicated that, absent sulfur or excessive sulfur would be not conducive to the synergistic growth for A. ferrooxidans and A. thiooxidans, and then not conducive to the uranium dissolution. Meanwhile, the sulfur-oxidizers could play an important role in the process of uranium synergistic bioleaching by mixed bacterial consortia. Additionally, the characteristics of mineral residue was detected by SEM-EDS. The results showed appropriate sulfur dosage would change the structure and improve the porosity of passivation substance. Lastly, the uranium dissolution kinetics and biochemical reaction mechanism was analyzed. It indicated that the biochemical reaction coupling iron and sulfur had a pleiotropic effect on the uranium dissolution from the ore particles, appropriate Fe/S ratio is the key factor for uranium bioleaching by chemoautotrophic acidophiles.

Variation of Bioaccumulation Ability of 2,2',4,4'-Tetrabromodiphenyl Ether by Marine Diatom Skeletonema costatum Under Different N:P Ratios

The growth, biochemical content and bioaccumulation quantity of 2,2',4,4'-tetrabromodiphenyl ether(BDE-47) in Skeletonema costatum were studied under different N:P ratios(1, 4, 16, 64 and 128). All cellular biochemical contents of S. costatum presented decreasing trend over cultivation time. At early stage of cultivation, the cellular protein, carbohydrate and lipid in S. costatum presented higher values in treatments of N:P=4 and 16. However, they were lower in these treatments at the late stage, but higher in treatments N:P=1 and 128. Similarly, BDE-47 levels per cell of S. costatum were higher in treatments of N:P=4 and 16 at early stage of cultivation, which were 3.8 and 3.7 ng(106 cells)-1, respectively. At the middle stage of cultivation, the BDE-47 level per S. costatum cell lowered; and it further reduced in the treatments of N:P=4 and 16 at the late stage with the values 0.6 and 0.5 ng(106 cells)-1, respectively. However, it rose in N:P=128, reaching up to 2.3 ng(106 cells)-1. Compared with BDE-47 per cell, BDE-47 per algal volume under different N:P ratios did not present obvious difference. The quantity BDE-47 accumulated per cell of S. costatum was positively correlated with protein, carbohydrate and lipid per cell; meanwhile, the BDE-47 per volume had a positive correlation with biochemical content per volume. The variation of bioaccumulation ability of BDE-47 in S. costatum can be explained by biochemical changes due to N:P ratios.

The Inhibitory Degree Between Skeletonema costatum and Dinoflagllate Prorocentrum donghaiense at Different Concentrations of Phosphate and Nitrate/Phosphate Ratios

Interactions between Skeletonema costatum (S. costatum) and Prorocentrum donghaiense (P. donghaiiense) were inves-tigated using bi-algal cultures at different concentrations of phosphate (PO4-P) and nitrate/phosphate (N/P) ratios. Experiments were conducted under P-limited conditions and the Lotka-Volterra mathematical model was used to simulate the growth of S. costatum and P. donghaiense in the bi-algal cultures. Both of these two species were inhibited significantly in bi-algal culture. The results of the simulation showed that the inhibitory degree of S. costaum by P. donghaiense was high when the concentration of PO4-P was low (0.1μmolL-1/2 d), but that of P. donghaiense by S. costaum was high with increased PO4-P supply (0.6μmolL-1/2 d). At low concen-tration of PO4-P (0.1μmolL-1/2 d), or high concentration of PO4-P (0.6μmolL-1/2 d) with high N/P ratio (160), the interactions be-tween S. costatum and P. donghaiense were dependent on the initial cell densities of both species. At high concentration of PO4-P (0.6μmolL-1/2 d) with low N/P ratio (25 or 80), S. costatum exhibited a survival strategy superior to that of P. donghaiense. The de-gree of inhibition of P. donghaiense by S. costaum increased with elevated N/P ratio when the medium was supplemented with con-centration 0.1μmolL-1/2 d of PO4-P. The degree of inhibition to P. donghaiense by S. costaum increased with elevated N/P ratio at low concentration of PO4-P (0.1 μmolL-1/2 d). This trend was conversed at high concentration of PO4-P (0.6μmolL-1/2 d). However, the degree of inhibition of S. costaum by P. donghaiense increased with the increased N/P ratio at different PO4-P concentrations (0.1μmolL-1/2 d and 0.6μmolL-1/2 d). These results suggested that both phosphate concentration and N/P ratio affected the competition between S. costaum and P. donghaiense: P. donghaiense is more competitive in environments with low phosphate or high N/P ratio and the influence of N/P ratio on the competition was more significant with lower phosphate concentration.

Effects of soil nitrogen:phosphorus ratio on growth rate of Artemisia ordosica seedlings

To address how the ratios of nitrogen and phosphorus (N:P ratios) in soil affect plant growth, we performed a two-factor (soil available N:P ratios and plant density) randomized block pot experiment to examine the relationships between soil N:P ratios, and the N:P ratios and growth rate of Artemisia ordosica seedlings. Under moderate water stress and adequate nutrient status, both soil N:P and plant density influenced the N:P ratios and growth rates of A. ordosica. With the increase of soil N:P ratios, the growth rates of A. ordosica seedlings decreased significantly. With the increase of soil N:P ratios, N:P ratios in A. ordosica seedlings increased significantly. While the nitrogen concentrations in the plant increased slightly, the phosphorus concentrations significantly decreased. With the increase of plant density, the shoot N:P ratios and growth rates significantly decreased, which resulted from soil N:P ratios. Thus, soil N:P ratios influenced the N:P ratios in A. ordosica seedlings, and hence, influenced its growth. Our results suggest that, under adequate nutrient environment, soil N:P ratios can be a limiting factor for plant growth.

Preparation of Fe_2P/Al_2O_3 and FeP/Al_2O_3 catalysts for the hydrotreating reactions

A 60%Fe/Al_2O_3 catalyst was prepared by the co-precipitation method.It was reduced by H_2 to produce metallic Fe,which was then sulfided by CS_2 to Fe_(0.96) S and Fe_3S_4 or phosphided by triphenylphosphine(PPh3) in liquid phases to Fe2 P and Fe P.It was found that the iron sulfides(Fe0.96 S and Fe_3S_4) exhibited the low activity for the hydrodesulfurization(HDS) reactions.The HDS activity was also low on the Fe(metal)/Al_2O_3 and Fe_2 P/Al_2O_3 catalysts since they were converted into Fe0.96 S and Fe_3S_4 during the HDS reactions.In contrast,the FeP/Al_2O_3 was found to be stable and active for the HDS reactions.In particular,Fe P/Al_2O_3 possessed significantly smaller Fe P particles than Fe P/C,leading to the significant higher HDS activity of FeP/Al_2O_3 than Fe P/C.

Effects of N:P ratio of Artemisia ordosica on growth influenced by soil calcium carbonate

Soil calcium carbonate(CaCO_3) has a strong solid phosphorus effect, and high content of CaCO_3 can significantly reduce the effectiveness of soil phosphorus. To reveal the limiting effect of soil CaCO_3 on the growth of plants on sand land and its mechanism of plant physiology, we performed pot experiments with a two-factor randomized block design and a three-factor orthogonal design for different soil CaCO_3 content treatments using Artemisia ordosica seedlings. In the experiments, we surveyed plant height, aboveground biomass, root length and root weight and analyzed N, P concentrations and RNA content of the seedlings, and discussed the relationships between relative growth rate(RGR) of the seedlings and N:P ratio as well as RNA. Results show that, the RGRs of plant height and above-ground biomass of the seedlings decreased significantly with the increase of soil CaCO_3 content, and those for root length and root weight decreased. The RGRs of plant height and above-ground biomass of the seedlings were significantly negatively correlated with leaf N:P ratios, but significantly positively correlated with leaf RNA content and leaf P concentrations. It can be seen that soil CaCO_3 is a stress factor for the growth of A. ordosica seedlings, and the growth response of the seedlings under the influence of soil CaCO_3 is in line with the Growth Rate Hypothesis.

Preparation of LiFePO_4 for lithium ion battery using Fe_2P_2O_7 as precursor

In order to obtain a new precursor for LiFePO4, Fe2P2O7 with high purity was prepared through solid phase reaction at 650 ℃ using starting materials of FeC2O4 and NH4H2PO4 in an argon atmosphere. Using the as-prepared Fe2P2O7, Li2CO3 and glucose as raw materials, pure LiFePO4 and LiFePO4/C composite materials were respectively synthesized by solid state reaction at 700 ℃ in an argon atmosphere. X-ray diffractometry and scanning electron microscopy（SEM） were employed to characterize the as-prepared Fe2P2O7, LiFePO4 and LiFePO4/C. The as-prepared Fe2P2O7 crystallizes in the Cl space group and belongs to β-Fe2P2O7 for crystal phase. The particle size distribution of Fe2P2O7 observed by SEM is 0.4-3.0 μm. During the Li^＋ ion chemical intercalation, radical P2O7^4- is disrupted into two PO4^3- ions in the presence of O^2-, thus providing a feasible technique to dispose this poor dissolvable pyrophosphate. LiFePO4/C composite exhibits initial charge and discharge capacities of 154 and 132 mA·h/g, respectively.

Synchronous enrichment of phosphorus and iron from a high-phosphorus oolitic hematite ore to prepare Fe-P alloy by direct reduction-magnetic separation process

In this study,direct reduction-magnetic separation process was applied to enrich phosphorus and iron to prepare Fe-P crude alloy from a high phosphorus oolitic hematite ore(HPOH).The results show that at lower temperatures and with absence of any of additives,Fe cannot be effectively recovered because of the oolitic structure is not destroyed.In contrast,under the conditions of 15%Na_(2)SO_(4)and reducing at 1050℃ for 120 min with a total C/Fe ratio(molar ratio)of 8.5,a final Fe-P alloy containing 92.40%Fe and 1.09%P can be obtained at an overall iron recovery of 95.43%and phosphorus recovery of 68.98%,respectively.This metallized Fe-P powder can be applied as the burden for production of weathering resistant steels.The developed process can provide an alternative for effective and green utilization of high phosphorus iron ore.

P-Δ effect on inelastic displacement ratio spectra for inelastic structures

For the evaluation of structures with known ductility demands,the constant-ductility displacement ratio spectra(CDDRS) are particularly useful for providing inelastic displacement ratios to estimate maximum lateral inelastic displacement demands from maximum elastic displacement demands.The CDDRS are computed for single-degree-of-freedom systems(SDOF) by considering or ignoring P-Δ effect for different ductility levels when subjected to 344 earthquake ground motions recorded in four site classes.The modified expressions of CDDRS for P-Δ effect are proposed.It is concluded that the P-Δ effect on CDDRS is significant,and the effect increases with the increase of ductility level.In the long-period region,the CDDRS ignoring P-Δ effect almost conforms to the equal-displacement rule.But in the case of higher ductility level,the CDDRS considering P-Δ effect are much higher than 1.0,which do not conform to the equal-displacement rule.