红外光度法测量糖液饱和温度的系统误差分析

对于红外光度法测量晶浆饱和温度、过饱和度的系统误差作了定性和定量的分析。系统误差来源包括：微晶的增溶效应（即Ｇｉｂｂｓ＿Ｔｈｏｍｓｏｎ效应）、细晶的预结晶作用、测温时的传热滞后、模／数转换精度及其它如操作过程引入的误差等。实验测量和定量分析的结果表明，对于蔗糖晶浆，用红外光度法测量其饱和温度的误差为２７２Ｋ～２７２．５Ｋ。

对差示光度法提高准确度的一种解释

分光光度法通常用于测定微量组分。当被测定溶液的浓度适中,吸光度A的值落在0.2—0.8(透光率T=15～65％)范围时,利用光度计进行吸光度测量的相对误差较小。当溶液的浓度太大,测得的A值不在上述范围时,测量的误差将大大增加。此时可用差示分光光度法进行测量提高准确度。为何差示法可以提高准确度呢?一般的分析化学教材都用扩展读数标尺来解释,这种解释较为直观,明了。但教材一般不说明扩展读数标尺的原理,这使一些学生感到困惑。有些教材进行了较为详细的探讨,但却直接引入一个差示透射率的定义,这也是一般学生不易理解的。本文从吸光度和透射率的定义出发,结合读数标尺的几何关系。对扩展读数标尺的原理加以简单说明。

Determination of the Trace Element Contents in Plants Using Atomic Absorption Spectrophotometer

The aim of the study is to investigate the contents of trace element Se, Cd, Pb in three plants including burdock, ginkgol and garlic via graphite furnace atomic absorption and standard addition method. The results show that Se in burdock stem, skin and leaf are 32.40, 48.63, 38.10 μg/g, respectively; Cd in burdock stem, skin and leaf are 0. 160 0, 0. 300 0, 0. 140 0 μg/g, respectively; Cd in burdock stem, skin and leaf are 2. 020, 3. 960, 2. 410 μg/g, respectively. In the ginkgo and ginko leaf, Se contents are 17.63 and 16.91 μg/g, respectively ; for Cd are 0. 181 0 and 0.2020μg/g, respectively ; for Pb are 3. 572 and 4. 021 μg/g, respectively. In garlic, Se, Cd and Pb are 73. 900 0, 6. 900 0 and 0. 390 0, respectively. All the standard deviations of measured results are below 2.3%, recovery rate are from 99% to 101%.

Measurement of Trace Manganese(Ⅱ) by the Catalytic Kinetic Spectrophotometric Method

A new kinetic spectrophotometric method is developed for the measurement of manganese(Ⅱ) in water. The method is based on the catalytic effect of manganese(Ⅱ) with the oxidation of weak acid brilliant blue dye(RAWL) by KIO4 using the Nitrilo triacetic acid(NTA) as an activation reagent. The optimum conditions obtained are 40 mgL-1 RAWL,1×10-4molL-1 KIO4,2×10-4 molL-1 Nitrilo triacetic acid(NTA),pH = 5.8,the reaction time of 3.00 min and the temperature of 20.0 ℃. Under the optimum conditions,the proposed method allows the measurement of manganese(Ⅱ) in a range of 0-50.0 ng mL-1 and with a detection limit of down to 0.158 ng mL-1. The recovery efficiency in measuring the standard manganese(Ⅱ) solution is in a range of 98.5%-102%,and the RSD is in a range of 0.76%-1.25%. The new method has been successfully applied to the measurement of manganese(Ⅱ) in both fresh water and seawater samples with satisfying results. Moreover,few cations and anions interfere with the measurement of manganese(Ⅱ). Compared with other kinetic catalytic methods and instrumental methods,the proposed method shows fairly good selectivity and sensitivity,low cost,cheapness,low detection limit and rapidity. It can be applied on boats easily.

Effect of Mn(II) on quartz flotation using dodecylamine as collector

Quartz is, in most cases, the major gangue mineral found in the manganese ore. Mn iron, dissolved from the surface of ore, will determine the interfacial properties of the particles and, thus, their flotation behavior. In this work, the effect of Mn2+ on quartz flotation was investigated through flotation tests. It was found that quartz can be depressed with Mn2+ and floated with dodecylamine in the pH region 7-8. In order to prove the validity of the findings, UV spectrophotometry, FTIR and SEM-EDS were carried out. UV spectrophotometry tests results show that Mn2+ can competitive adsorb with RNH3+ in the surface of quartz at acidic and neutral pH values. The FTIR measurements and SEM-EDS analysis indicate that Mn2+ forms precipitation and adsorbs on the negatively charged quartz surface, it induces quartz recovery dropping in alkaline pH. Furthermore, in the case of sodium hexametaphosphate(SH), sodium silicate or citric acid, the effects of Mn2+ were also studied. This depression in the given Mn2+ did not disappear. Citric acid is an appropriate modifier to separate quartz depressed by Mn2+ from other ores at pH 7.

Membrane preconcentration of iron in seawater samples and on-site determination in spectrophotometry

A novel method for on-site determination of trace iron was developed using membrane preconcentration and spectrophotometric detection. Fe（II）-ferrozine complex was reacted with cetyltrimethylammonium bromide （CTAB） to form a Fe（II）-ferrozine-CTAB paired compound, which was collected on a membrane by filtration under vacuum. The membrane was immersed in 2 mL of ethanol-nitric acid and the absorbance of the solution measured for quantitative analysis. Various factors affecting the iron collection and determination were investigated. With different sample preconcentration volumes, the range of determination was broadened to 0.5-120 ~tg/L. The detection limit of this method reached 0.19 ktg/L and the recoveries were between 97.2 and 109% when the concentration enrichment was about 45. The relative standard deviation （n = 7） was 1.9% for samples containing 10 ~g/L Fe. Twelve seawater samples were analyzed on-site using the proposed method, and two were also analyzed in inductively coupled plasma mass spectrometry. No significant difference was shown between the two methods by the Student＇s t-test. The method has also been used on-site for iron enrichment experiments with phytoplankton and concluded to be simple, accurate and inexpensive.

A device for fluorescence temperature measurement based on fast fourier transform

A sapphire fiber thermal probe with Cr^3＋ ion-doped end was grown using the laser heated pedestal method. The fluorescence thermal probe offers advantages of compact structure, high performance and the ability to sustain high temperature from the room temperature to 450℃. Based on the fast fourier transform （FFT）, the fluorescence lifetime is obtained from the tangent function of the phase angle of the first non-zeroth item of FFT result. Compared with other traditional fitting methods, our method has advantages such as fast speed, high accuracy and being free from the influence of the base signal. The standard deviation of FFT method is about half of that method. In addition, since the FFT method is immunity to analysis can be skipped. of the Prony method and close to the one of the Marquardt the background noise of the signal, the background noise

A New Method for Measurement of Local Solid Flux in Gas-Solid Two-phase Flow

Previous works have shown that the suction probe cannot be used to accurately measure the upward and downward particle fluxes independently. A new method using a single optical probe to measure the local solid flux is presented. The measurement of upward, downward and net solid fluxes was carried out in a cold model circulating fluidized bed (CFB) unit. The result shows that the profile of the net solid flux is in good agreement with the previous experimental data measured with a suction probe. The comparison between the average solid flux determined with the optical measuring system and the external solid flux was made, and the maximum deviationturned out to be 22%, with the average error being about 6.9%. These confirm that the optical fiber system can be successfully used to measure the upward, downward and net solid fluxes simultaneously by correctly processing the sampling signals obtained from the optical measuring system.

STUDY ON THE DETERMINATION OF TRACE BISMUTH(III) BY THIN-LAYER RESIN PHASE SPECTROPHOTOMETRY

In this paper, a new thin-layer ion-exchange resin phase analytical method is introduced. It is based on that, the bismuthous cation can associate with iodic anions, so as to formed an anion complex [BiI4-] in a strong acidic environments. This anion complex can also exchanges with a weaker anions on the surface active site of anion exchange resin, so that a [R+] [BiI4-] solid phase binary associational system is produced. Owing to the solid system is a great many dispersive particulates, it can be pressed to a thin-layer by press tools of the so called 搕hin-layer resin phase?or 搑esin phase? and using this solid association system spectrophotometry for the determination of trace metals. So it can increase the analytical sensitivity. This association system exhibits maximum absorbance at 460nm, and obeys Beer抯 law over the concentration range 0.01ug/ml^1.20ug/ml of bismuthous(III). It has a molar absorptivity of 7.1×105 [L/mol穋m]. It indicated the resin phase spectrophotometry is a sensitive analytical method for trace bismuthous. It is 18 times higher than routine aqueous spectrophotometry. The relative standard deviations is 1.82% (n=6) for the measurements of 0.5ug/ml Bi(III). The detection limit of Bismuthous(III) is 1.4×10-8mol/L. The method has applied to the analysis Bi(III) in environmental water samples.

Determination of Cholesterol Content in Waste Fat by Dual-wavelength Spectrophotometry

[Objective]The aim was to find a way to measure the cholesterol content in deserted oil.[Method]Dual-wavelength spectrophotometry method was used for the determination of cholesterol in edible oil.630 nm and 720 nm were set as target band and reference band in this method,respectively.The result was compared to liquid chromatography method.[Result]The relative standard deviation(RSD)was at 1.26% and recovery was between 101.9% and 110.7%.Linear range was 8.0-40.0 μg/ml.The tested result was close to the result of liquid chromatography.[Conclusion]It was proved that this method was easy,fast and accurate.The disturbance of sitosterol was eliminated without isolation.It can be used for fast identification of the authenticity of waste fat.

3D Surface Morphology Measurement and Auto-focusing System

When interference microscope measures the surface rough of the micromechanical device, as soon as the work distance of interference microscope and the depth of field is shortened, the interference images become slur for the measured object if there has small interference after clear focus. The auto-focusing system is introduced into the interference microscope, the system can obtain high definition interference image rapidly,and can improve the measuring velocity and measuring precision. The system is characterized by auto-focusing range of ±150 μm, auto-focusing precision of ±0.3 μm, auto-focusing time of 4～8 s.

Development of 2D Temperature and Concentration Measurement Method Using Tunable Diode Laser Absorption Spectroscopy

Exhaust gas temperature is an important factor in NOx, THC and PM emissions of engines. Especially 2D temperature and concentration distribution plays an important role for the engine efficiency. A thermocouple is intrinsically a point temperature measurement method and noncontact 2D temperature distribution cannot be attained by thermocouples. Recently, as a measurement technique with high sensitivity and high response, laser diagnostics has been developed and applied to the actual engine combustions. With these engineering developments, transient phenomena such as start-ups and load changes in engines have been gradually elucidated in various conditions. In this study, the theoretical and experimental research has been conducted in order to develop the noncontact and fast response 2D temperature and concentration distribution measurement method. The method is based on a Computed Tomography （CT） method using absorption spectra of water vapor at 1388 nm. It has been demonstrated that the method has been successfully applied to engine exhausts to measure 2D temperature distributions.

Homemade versus Commercial Jarred Baby Foods with Regard to Nitrites and Nitrates Content

This paper presents results of nitrites and nitrates determination in two types of baby foods： commercial products in jars and their homemade conventional counterparts. Nitrites levels in all analyzed samples were below of the detection limit （〈 0.9 mg/kg） of applied spectrophotometric method with Griess reagent. Nitrates contents in commercial products ranged： 9.1-38.1 mg/kg while in homemade baby foods levels between 26.6 mg/kg and 118.8 mg/kg were obtained. All the contents of nitrates were lower than the EU legislation maximum limit （200 mg/kg）. Comparison of each type of commercial product with its homemade counterpart baby food evidenced significant differences （p 〈 0.05） in average nitrates levels in favor of the first type. Apart from determining and comparing the levels of nitrates in the baby food samples also risk assessment for an average 6-months old infant to nitrates exposure was conducted. The estimated nitrates intake with a typical portion of 200g of baby food ranged between 6% and 25.7% of acceptable daily intake for commercial and from 18.0% to 80.3% for homemade ones.

Evaluation of photon beam dose calculation accuracy of treatment planning systems using in vivo dosimetry

Objective The treatment planning system currently represents one of the basics of radiation therapy,because it is the only method to estimate patient dose delivery fast forward and accurately represent estimated tumor location of the tumor with the possibility of estimating densities in the tissue surrounding the tumor to overcome dose calculation defects but radial estimated the patient.Despite the flaws associated with the systems and calculates the dose of your programs in all programs currently existing in the world.Than necessary,to the existence of a review of the accuracy of accounts and how to confirm the radiation dose to the patient programs.Methods A total of 35 cancer patients were considered for this study,with 245 field measurements made with low-and high-energy diode detectors for brain and prostate cases.The treatments for all patients were planned using Eclipse Treatment Planning System version 13.6.Results Of the 105 field measurements made for the prostate cancer patients,16 included discrepancies outside the ±5% action level.Of the 145 measurements taken of the brain cases,there were four outside the ±5% action level.The results indicated a higher degree of accuracy.The study revealed that,for the prostate measurements,the higher discrepancy in the doses for the particular fields(exceeding the action level) may have been due to the isocenter being very close to the jaws and multi-leaf collimator of the linear accelerator machine.As a result,scatter from the jaws and the multi-leaf collimator could have contributed to the high dose delivered to the diode;hence,a probable higher discrepancy of the dose in more brain cases due highest quality of VMAT technique and fixation system.Conclusion A greater percentage of the observed discrepancies were well within the set tolerance level.However,it is recommended that the positioning of the diode on the patient's skin and the angular sensitivity of the diodes be reconsidered.It is also recommended that a more accurate calculation of expected diode values be performed,especially for fields that pass through the table.These efforts would achieve action levels of ±5%.

Study on the Determination of Trace Ni(II) by the Catalytic Kinetic Spectrophotometric Method

A new kinetic spectrophotometric method has been developed for the determination of trace Ni （Ⅱ in natural water. The method is based on the catalytic effect of Ni （Ⅱ） on the oxidation of weak acid brilliant blue dye （RAWL） by KIO4 in acid medium. The concentration of nickel （Ⅱ） can be determined spectrophotometrically by measuring the decrease of absorbance of RAWL at λ = 626 nm using the fix-time method. The influencing factors are investigated by the orthogonal experimental design. The obtained optimum analytical conditions are： pH = 2.00, CRAWL = 5.00×10^-5 mol·L^-1, c KlO4 = 2.00× 10^-5 mol·L^-1, the reaction time t= 10min and the temperature T = 25 ℃. Under the optimum conditions, the developed method allows the measurement of Ni （Ⅱ） in a range of 0 - 40.0ngmL1. The standard deviation of eleven independent measurements of blank reaction is S = 3.08× 10^-3 and the limit of detection is 2.20ng·mL^-1. The relative standard deviations （RSDs） in six replicate determinations of 5 ngmL-1 and 8 ngmL1 Ni （Ⅱ） are 2.87% and 1.11%, respectively. Moreover, the experiments show few cations and anions can interfere with the measurement of Ni （Ⅱ）. The recovery efficiencies of this method are in a range of 97.0%-102.5% in freshwater samples. But there is a decreasing effect, which is about 0.2 times the added Ni （Ⅱ） in seawater medium. After reasonable calibration this processing method is used for the determination of Ni （Ⅱ） in seawater samples successfully. The results show this developed method has high accuracy and precision, high sensitivity, large range of linearity and high speed. The method can, therefore, be employed at room temperature.

Verification of Insulation Oil Reclamation by Turbidity and Spetrophotometry Measurements

Oil reclamation with Fuller＇s earth is known to have an improved effect on conditioning aged oil. In this paper it is shown that aged oil reclamation effectiveness can be monitored with turbidity and spectrophotometry measurements. These low cost testing techniques offer a useful tool to quantify the effect of Fuller＇s earth. Experimental investigations performed in laboratory conditions have shown that the quality of properly reclaimed aged oil can compete with that of new oils. Thus, in addition to extending the life cycle of this non-renewable resource, on-line reclamation of liquid might also prevent the premature ageing of paper insulation. Studying the stability of reclaimed service aged oil samples emphasized the important role played by Fuller＇s earth absorption capability.

A new distance correction method for sulfur analysis in coal using online XRF measurement system

When X-ray fluorescence （XRF） technology is used to measure the sulfur concentration in coal online, the measurement accu- racy is affected by the coal＇s uneven surface and the particle size. In order to improve the accuracy of sulfur concentration measurement, an online measurement system, consisting of a portable X-ray fluorescence instrument and an auxiliary distance correction module, was developed in this paper. By measuring the standard coal samples of known sulfur concentration, we obtained a calibration curve that can be used to analyze the sulfur concentration. We studied the relationship between the X-ray fluorescence intensity （I） and the distance （D） from surfaces to instrument. The results showed that there was a good linear re- lationship between 1 and D when the sulfur content was certain. Based on these knowledge, the distance correction formula of X-ray fluorescence intensity was proposed. By applying the distance correction formula to experimental sulfur concentration measurement, we demonstrated that the measurement accuracy can be significantly increased.

Noninvasive photoacoustic measurement of absorption coefficient using internal light irradiation of cylindrical diffusing fiber

Absorption coefficient of biological tissue is an important parameter in biomedicine, but its determination remains a challenge. In this paper, we propose a method using focusing photoacoustic imaging technique and internal light irradiation of cylindrical diffusing fiber(CDF) to quantify the target optical absorption coefficient. Absorption coefficients for ink absorbers are firstly determined through photoacoustic and spectrophotometric measurements at the same excitation, which demonstrates the feasibility of this method. Also, the optical absorption coefficients of ink absorbers with several concentrations are measured. Finally, the two-dimensional scanning photoacoustic image is obtained. Optical absorption coefficient measurement and simultaneous photoacoustic imaging of absorber non-invasively are the typical characteristics of the method. This method can play a significant role for non-invasive determination of blood oxygen saturation, the absorption-based imaging and therapy.

On-line solid-phase extraction using alizarin violet functionalized silica gel for determination of trace lead in environmental samples and wastewater by sequential injection spectrophotometry

Trace of Pb(Ⅱ) has been on-line separated and enriched from environmental samples and wastewater by using the self-made alizarin violet functionalized silica gel micro-column coupling with a sequential injection sampling technology. The determination is based on the color reaction of Pb(Ⅱ) with iodide and crystal violet to form an ionic association complex in the presence of polyvinyl alcohol and hydrochloric acid. The use of the microcolumn can prevent the interference of most familiar metal ions, and therefore improve the selectivity and sensitivity of this analytical technique. The proposed method was used for the determination of Pb(Ⅱ) in environmental samples and wastewater. No statistically significant difference was observed between the results determined by the present method and atomic absorption spectrometry.

Thermal Characteristic Identification of an Alcohol Flame by Measuring its Density Gradient in Shack-Hartmann Optical System

Understanding the flame structure for different combustion in industries has drawn the increasing attention around the world.Particularly,for increasing the recent interest of using the hydrogen fuelled vehicles in recent world,structural analysis of flame in combustion chamber has attracted the attention of researchers.However,the high flame temperature and strong flame emissions increase the experimental difficulties,especially,in all kinds of intrusive measurement systems for determining the flame structures and flame temperatures.Therefore,a non-intrusive laser interferometer technique based on Shack-Hartmann optical system has been proposed to measure the thermal characteristic of a flame structure.In the present study,a low-stretched diffusion flame of methanol burner has been used.Shack-Hartmann optical system is a type of wave front sensor.It is commonly used in adaptive optical systems.It consists of an array of lenses to focus the image onto a photon sensor (photo-detector) at the focal plane and measures the wave front tilt.The major objective of the present study is to develop a laser interferometer measurement technique for analyzing the flame structure and its temperature propagation by measuring the density gradient of the flame.Optical interferometer technique is a potential candidate for the non-invasive measurement.In the present paper,a novel method for the measurement of density gradient in flame by using Shack-Hartmann optical system is proposed.A collimated laser beam that has been passed through the flame is tilted due to the density gradient inside the flame.A CCD camera (CCD photo sensor) has been used to observe the wave front tilts at the focal plane.