Nitrogen-doped hierarchically porous carbon obtained via single step method for high performance supercapacitors

In the present work, nitrogen doped hierarchically activated porous carbon (APC) samples have been synthesized via single step scalable method using ethylene di-amine tetra acetic acid (EDTA) as precursor and KOH as activating agent. Activated porous carbons with different pore sizes have been developed by varying the activation temperature. SEM, TEM and SAXS analysis suggest that with variation of activation temperature, a hierarchical porous structure with interconnected meso-pore and micro pores has been achieved. The sufficiently high surface area of the synthesized materials provides active sites to enhance the diffusion of ions between the electrolyte and the carbon electrodes. The electrode prepared at 800 °C activated sample exhibited highest specific capacitance of 274 Fg^-1 in two electrode setup, at a current density of 0.1 Ag^-1 in 1 M aqueous H₂SO₄. Along with this, it showed maximum energy density of 9.5 Whkg^?1 at a power density of 64.5 Wkg^-1. The remarkable electrochemical performance reveals that the synthesized nitrogen doped activated carbon electrodes derived from EDTA can be tuned to have optimum pore structure and pore size distribution for better electrochemical performance, so it can be considered as a potential electrode material for applications in electrochemical energy storage.     

稀土溶液标准物质的研制

选择7种稀土元素:La、Ce、Sm、Eu、Yb、Lu、Y为研究对象,采用高纯稀土氧化物(≥99 99%)为原料,经ICP MS及ICP AES对纯度进行分析后,分别制备成浓度为1000μg mL的稀土溶液标准物质。采用准确、可靠并能溯源的EDTA络合滴定法进行量值核对、均匀性及稳定性检验。对标准物质的不确定度进行了全面的评定。研制的稀土溶液一级标准物质,总不确定度优于0 6%,稳定性达两年以上。     

关于新建炉EDTA低浓度清洗的探讨

阐述了EDTA清洗锅炉的基本原理,低浓度清洗新建炉的工艺、方法及控制要点,EDTA低浓度清洗与协调EDTA清洗的经济性比较,为新建炉EDTA低浓度清洗探索了方向。     

硫酸锶晶体生长动力学研究

为了从控制晶体生长角度，说明制备纳米硫酸锶沉淀体系中存在的EDTA对产品粒径的影响作用，根据过程机理，用恒组成法研究硫酸锶晶体生长动力学。根据叠加模型和弱化模型，建立体系中有EDTA存在时，硫酸锶沉淀过程的晶体生长动力学模型。结果表明，硫酸锶沉淀过程中晶体生长属于表面反应控制机理。EDTA存在能降低晶体生长速率，有利于减小粉体粒径。     

Effect of pH, sulfate and sodium on the EDTA titration of calcium

The ethylenediaminetetraacetic acid (EDTA) titration method limits the measurement of calcium concentration to 50 mg/l in water. However, various acids and salt solutions are used in the investigation of the durability of concrete, and the adaptability of the EDTA titration method to determine the calcium in these solutions must be investigated. Hence, the purpose of this study was to investigate the interfering effects of hydrochloric acid, sulfuric acid, sodium chloride and sodium sulfate on measuring the calcium in the aqueous leaching solutions using the EDTA titration method. The calcium standard solutions were prepared using CaCl₂ with initial pH from −0.8 to 7 and calcium concentration up to 160 mg/l. Sulfuric acid and hydrochloric acid were used to prepare calcium solutions with lower pH. Salt solutions with 3% NaCl and 3% Na₂SO₄ were used to evaluate the interfering effects of salt elements such as sulfate and sodium on the EDTA titration. Results indicated that the EDTA titration method was reliable in measuring the calcium up to 160 mg/l, the maximum concentration investigated in this study, in hydrochloric acid with pH higher than zero and 3% sodium chloride solution. Sulfuric acid with pH higher than zero and 3% sodium sulfate solutions showed 3% to 4% less calcium in the solutions. Acid solutions with pH less than zero showed interference with calcium measurement.     

Oxidative flavour deterioration of fish oil enriched milk

The oxidative deterioration of milk emulsions supplemented with 1.5 wt‐% fish oil was investigated by sensory evaluation and by determining the peroxide value and volatile oxidation products after cold storage. Two types of milk emulsions were produced, one with a highly unsaturated tuna oil (38 wt‐% of n‐3 fatty acids) and one with cod liver oil (26 wt‐% of n‐3 fatty acids). The effect of added calcium disodium ethylenediaminetetraacetate (EDTA) on oxidation was also investigated. Emulsions based on cod liver oil with a slightly elevated peroxide value (1.5 meq/kg) oxidised significantly faster than the tuna oil emulsions, having a lower initial peroxide value (0.1 meq/kg). In the tuna oil emulsions the fishy off‐flavour could not be detected throughout the storage period. Addition of 5—50 ppm EDTA significantly reduced the development of volatile oxidation products in the cod liver oil emulsions, indicating that metal chelation with EDTA could inhibit the decomposition of lipid hydroperoxides in these emulsions. This study showed that an oxidatively stable milk emulsion containing highly polyunsaturated tuna fish oil could be prepared without significant fishy off‐flavour development upon storage, provided that the initial peroxide value was sufficiently low.     

EDTA滴定法精确测定可溶性氯化物中氯含量

介绍了利用EDTA滴定法精确测定可溶性氯化物中氯含量的原理、条件和方法。试样溶解后,先在强酸性介质中用AgNO3沉淀Cl-离子,沉淀过滤后,加入过量Ni(CN)42-发生置换反应,然后在pH9.5的氨性缓冲溶液中,以紫脲酸铵为指示剂,用EDTA标准溶液滴定置换出的Ni2 离子。结果表明,改进后的本法,准确、干扰小、终点现象明显,是一种准确的测氯方法。测定结果的变异系数仅为0.18%,回收率为98.3%～100.9%。     

EDTA络合滴定法快速测定碳酸锆中锆铪含量

锆铪氧化物含量的测定通常采用苦杏仁酸[C6H5CH（OH）COOH]重量法。该法经典、准确,但操作烦琐,分析时间长,对日常生产、入库或销售不利。乙二胺四乙酸二钠（EDTA）络合滴定法（容量法）操作简便、快速、准确,适合日常检验。但用基准氧化锌、高纯二氧化锆或氯氧化锆来标定EDTA时,测定结果偏低。采用重量法和容量法相结合,先用重量法测定锆铪氧化物含量,以已知锆铪氧化物含量的碳酸锆作标定物,再标定EDTA标准溶液的滴定度,用此EDTA标准溶液测定相同原料生产的碳酸锆。该法简便、快速、准确,试剂安全性好。     

EDTA在尿素换热设备清洗中的应用

草酸法清洗换热设备垢层时对设备腐蚀严重。EDTA能与积垢中的铁离子反应生成溶于水的络合离子,达到清洗积垢的目的,对设备腐蚀程度也小,通过EDTA、Fe含量的变化可判断清洗程度。     

Preparation and Kinetic Considerations for the Dissolution of Cr‐substituted Iron Oxides in Reductive‐complexing Formulations

The dissolution rate coefficients of Cr‐substituted (0‐20 at.% Cr) iron oxides viz. hematite and magnetite were determined by using an inverse cubic rate (ICR) law applicable for spherical particles as well as by a general kinetic equation (GKE) applicable for polydispersed particles. An attempt is made to compare both the treatments for different kinds of dissolution profiles obtained by employing oxides with narrow particle size distribution in V(II)‐EDTA and citric acid‐EDTA‐ascorbic acid formulations at 353±5K. The dissolution profiles could be classified into three types based on the nature of oxide and formulations. It is observed that both ICR and GKE treat the dissolution course as a function of decrease in fraction of undissolved mass, m/m₀. The dissolution rate coefficients determined by ICR and GKE have shown the similar trend of decrease with increasing Cr content of the oxides and was ascribed to lattice stabilization.