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1.
为进一步提升图像比色法测定补铁药物中铁含量的准确性及普适性,考察了拍摄环境对结果的影响,确定了适用于图像比色分析的定量参数,比较使用不同容器来盛装溶液所获得的比色结果,在最优条件下测定了实际样品中铁的含量及加标回收率。结果显示,获得可靠数据的关键是将标准溶液、待测液以及空白溶液拍摄在同一张图片上;由溶液图像R值换算的吸光度值与浓度具有最佳的线性关系;分析以比色皿、试管、点滴板为容器获得的溶液图片,都能得到适合于定量比色分析的数据;测定的加标回收率大于95%。该方法操作简便,测定结果准确,可在各种条件下的高中化学实验室中开展。 相似文献
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根据溶液中有色物质颜色值与其质量浓度成正比的原理及数字图像红绿蓝色彩模式,通过采集样品溶液的图像信息,采用图像比色法对有色溶液进行定量分析。以蓝色硫酸铜溶液为研究对象,在实验箱内采集图像和建立统计回归模型。结果表明:方法测量误差为5%,线性范围为10.0~50.0g·L-1,相关系数大于0.990。 相似文献
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镝铁合金中铁含量的检测方法通常以人工滴定为主,但这种方法存在耗时长、操作繁琐、人眼判断滴定终点差异性等问题。本文研制了一种以图像处理为基础的镝铁中铁含量自动分析仪,实现了样品前处理、滴定、终点判定等过程一体化与自动化,减少了人工操作。可同时进行五个样品试验,提高了滴定效率。采用CCD工业相机摄取溶液图像,实现化学反应过程中溶液颜色的自动化识别,运用颜色分量二阶矩阈值和像素点数量排除溶液颜色交替变化的干扰,并基于直方图对比得到相似度进行滴定终点的判定,能够有效、准确地实现化学反应过程中溶液颜色的自动化识别。使用参考值为19.47%-20.25%的镝铁合金样品进行试验,与手工滴定结果比对验证,精密度测量结果相对标准差在0.21%以内,正确度测量结果误差在0.15%以内,满足国标《镝铁合金化学分析方法第4部分:铁量的测定 重铬酸钾容量法》(GB/T26416.4—2010)的精度要求。 相似文献
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根据Flory等效流体力学球模型及其粘度理论,对溶液中大分子链尺寸进行了研究,导出了一个能在整个溶液浓度范围内适用的形式简单的大分子链尺寸与溶液浓度间定量关系新方程。由该方程计算分子量为1.1×10~5的聚苯乙烯在不同浓度的甲苯溶液中的R_G值与Hayashi等人的小角X散射实验值很接近;也与King等人由中子散射法测得的实验值基本一致。相比较,由本模型所得的预言结果比其它理论模型所得的结果更为满意。 相似文献
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建立了光度法测定硫普罗宁的新方法。研究表明:在SCN-和KNO3存在下,控制溶液pH4.0,Cu(II)被硫普罗宁还原生成的Cu(I)与SCN-反应形成CuSCN沉淀,该沉淀能浮在水相表面。通过测定溶液中剩余Cu(II)的量,可以测定硫普罗宁的含量。吸光度与硫普罗宁浓度之间存在良好线性关系。线性方程:A=4.898-0.3616ρ(μg/mL),线性范围为0.25~12.0μg/mL,相关系数R=0.9993,检出限为0.16μg/mL。该方法可直接用于药物中硫普罗宁含量的测定及其药代动力学行为研究。 相似文献
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在弱酸介质中,硼、苯羟乙酸和[Fe(Phen)3]2+(phen:邻二氮菲)缔合生成具有较大疏水基团的化合物,用1,2-二氯乙烷萃取,再用去离子水反萃取,再用火焰原子吸收光谱法测定水相中铁,由此间接测定硼的含量.硼的质量浓度在0.05~3.24 mg·L-1范围内呈线性,方法检出限(3S/N)为0.036 mg·L-1.应用此方法测定了硼钢标准样品中硼含量,测得结果与已知值相符. 相似文献
11.
A. V. Tvardovskii A. A. Fomkin Yu. I. Tarasevich I. G. Polyakova V. V. Serpinskii I. M. Guseva 《Russian Chemical Bulletin》1992,41(6):987-991
The changes in the thermodynamic functions of the sorbents were calculated for the first time from measurements of the deformations of vermiculite during the sorption of water vapor and adsorption-calorimetric data.Institute of Physical Chemistry, Russian Academy of Sciences, 117915 Moscow. Institute of Colloid Chemistry and the Chemistry of Water, Academy of Sciences of the Ukraine, 252180 Kiev. Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 6, pp. 1270–1275, June, 1992. 相似文献
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We have summarized results of many experimental investigations of the thermodynamics of ionization of H2O(liq.) from 0–300°C and from 1.0 atm to nearly 8000 atm. Results of these investigations (equilibrium constants, enthalpies of ionization, heat capacities, partial molal volumes, and compressibilities) have been used for a number of thermodynamic calculations. It is particularly noteworthy that it is possible to use thermal data from 0–145°C with an equilibrium constant for 25°C in calculating reasonably accurate equilibrium constants for temperatures as high as 300°C. Similarly, it is possible to use volumetric data that refer to 1.0 atm in calculating useful equilibrium constants that apply for pressures as high as 2000 atm.Much of the work reported here was done while the author was on leave at the University of Lethbridge. 相似文献
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W. Zielenkiewicz A. Zielenkiewicz K. L. Wierzchowski 《Journal of solution chemistry》1993,22(11):975-981
Enthalpies of solution in water H
sol
o
and enthalpies of sublimation H
sub
o
were determined for a number of crystalline derivatives of uracil: 1,6-dimethyluracil (m
2
1,6
Ura), 1,3,6-trimethyluracil (m
3
1,3,6
Ura), 6-ethyl-1,3-dimethyluracil (e6m
2
1,3
Ura), 6-propyl-1,3-dimethyluracil (pr6m
2
1,3
Ura) and 6-butyl-1,3-dimethyluracil (but6m
2
1,3
Ura). Standard enthalpies of hydration H
hydr
o
and standard enthalpies of interaction H
int
o
of the solutes with their hydration shells were calculated. The data obtained show that dependence of H
int
o
on the number of-CH2- groups of n-alkyl chain added upon substitution of diketopyrimidine ring is nonlinear. This finding is discussed in connection with results of X-ray diffraction structure determinations for the crystalline compounds. 相似文献
14.
G. Venkoba Rao M. Balakrishnan N. Venkatasubramanian P. V. Subramanian V. Subramanian 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1):83-85
Abstract The signals for the α, β, and γ protons of pyridine exhibit a downfield shift in DMSO-d6, compared to CCl4 as solvent, the order being γ > β > α. This is attributed to an interaction between the positive end of the DMSO dipole and the lone pair of electrons on the ring nitrogen. This effect is also reflected in the faster rate of alkaline hydrolysis of ethyl isonicotinate over ethyl nicotinate and ethyl picolinate in aqueous DMSO relative to aqueous ethanol. Similar solvent effects are also observed in the pmr spectrum of pyrazine. 相似文献
15.
The protonation of leucoemeraldine in power form and in N-methylpyrrolidinone (NMP) solution by HCIO4 and HBF4 has been studied by x-ray photoelectron spectroscopy (XPS), infrared (IR), and ultraviolet (UV)-visible absorption spectroscopy. In powder form, less than 25% of the amine nitrogens can be protonated in the absence of oxygen. The effects of oxygen on the degree of protonation and the distribution of amine and imine units upon deprotonation of the salt are investigated. The degree of protonation in leuccemeraldine can be increased to about 50% with 3 M HCIO4, similar to that achievable with emeraldine base in powder form. In NMP solution, leucoemeraldine is easily oxidized by dissolved oxygen. Protonation of both leucoemeraldine and emeraldine base in NMP solutions results in metastable species which gradually undergo deprotonation. The resulting products are affected by the O2 content of the solutions. © 1993 John Wiley & Sons, Inc. 相似文献
16.
Earl M. Woolley John O. Hill William K. Hannan Loren G. Hepler 《Journal of solution chemistry》1978,7(5):385-393
We have made calorimetric measurements of enthalpies of dilution of aqueous iodic acid and have used these results for evaluation of the standard enthalpy of ionization of HIO3(aq.). We have also made calorimetric measurements of enthalpies of addition of perchloric acid solution to aqueous solutions of KIO3, KNO3, NaIO3, and NaNO3 and have used these results to obtain further values for the standard enthalpy of ionization of HIO3(aq.). On the basis of all these results, we have selected Ho=–660±125 cal-mole–1 as the best available standard enthalpy of ionization of HIO3(aq.) at 298.15°K, compared to the previously accepted –2400 cal-mole–1. Using the best available K=0.157 for ionization, we also obtain Go=1097 cal-mole–1 and So=–5.9 cal-oK–1-mole–1 for ionization of HIO3(aq) at 298.15°K.On study leave from Department of Inorganic and Analytical Chemistry, LaTrobe University, Bundoora, Victoria, 3083, Australia, to University of Lethbridge.On study leave from Department of Chemistry, University of Wollongong, Wollongong, N.S.W. 2500, Australia, to University of Lethbridge. 相似文献
17.
Sergey P. Verevkin Wei-Hong Peng Hans-Dieter Beckhaus Christoph Rüchardt 《Structural chemistry》1996,7(5-6):397-404
The standard enthalpies of combustion c
H
o of aliphatic diacetates1 and aromatic diacetates2 were measured calorimetrically. The enthalpies of vaporization vap
H
o or sublimation sub
H
o of1 and2 were obtained from the temperature function of the vapor pressure measured in a flow system. From f
H
o(g) of1 and2 new values of group increments for the estimation of standard enthalpies of formation of these classes of compounds were derived. The geminal interaction energy between the geminal acyloxy groups shows no anomeric stabilization.Geminal Substituent Effects, Part 12, for part 11 see Ref. 7. 相似文献
18.
An equation for the internal pressure acting on an adsorbate in micropores was obtained on the basis of the assumption that the chemical potential of an adsorbate in micropores is equal to that in an equilibrium gas phase and using the Dubinin-Radushkevich equation. The empirical relation between the characteristic adsorption energy and the half width of pores was expressed in terms of internal pressure and diameter of adsorbate molecules. The two-dimensional pressure was calculated for micropores with plane-parallel walls, where the width of a micropore coincides with the diameter of an adsorbate molecule. The results obtained were compared with the two-dimensional pressure of a monolayer on a free planar surface for an adsorbate and adsorbent of the same nature.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1928–1930, October, 1995. 相似文献
19.
根据盐类水解关系式和水的离子积计算公式,建立了计算盐类水解度和水解产物离解常数的完全方程式。计算值同实验值比较,钾明矾溶液水解度平均偏差为0.6%,离解常数pK_b=11.6±0.1,水的离子积pK_w平均偏差小于0.06,从而改进了苏联的计算公式。 相似文献