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分析化學(簡體書)
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分析化學(簡體書)

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定  價:NT$ 150 元
優惠價:87131
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本書是根據教育部關于高等學校本科教學質量工程要重視雙語教學的文件精神,參考國外優秀英文原版分析化學教材,結合雙語教學的實踐經驗編寫而成的雙語教材。
全書共12章,涵蓋內容與國內高等學校化學、化工類分析化學教材基本一致,包括緒論,誤差與實驗數據的處理,滴定分析總論,酸堿平衡,酸堿滴定,絡合滴定等內容。另外,第12章對環境污染物的分析進行了全面的介紹。為便于學生學習,每章后均設有中文撰寫的“本章小結”,介紹本章的基本要求、基本概念、主要計算公式等內容。
本書可作為高等院校化學、化工專業分析化學課程的教材,特別適合開設分析化學雙語課程的高等院校,亦可供理、工、農高等院校的相關專業作為教材或教學參考書,也可供從事分析化學工作的科技人員閱讀和參考。

名人/編輯推薦

《分析化學》共12章,涵蓋內容與國內高等學校化學、化工類分析化學教材基本一致,包括緒論,誤差與實驗數據的處理,滴定分析總論,酸堿平衡,酸堿滴定,絡合滴定等內容。另外,第12章對環境污染物的分析進行了全面的介紹。為便于學生學習,每章后均設有中文撰寫的“本章小結”,介紹本章的基本要求、基本概念、主要計算公式等內容。本教材由魏云霞、馬明廣共同編寫。

目次

1?1What is analytical chemistry1
1?2Measurement of the analyte2
1?3Range2
1?4The analytical perspective3

2?1Determinate errors5
2?2Indeterminate errors6
2?3Accuracy and precision6
2?3?1Ways of expressing accuracy7
2?3?2Ways of expressing precision8
2?4The distribution of measurements and results9
2?4?1Populations and samples10
2?4?2Probability distributions for populations10
2?4?3Confidence intervals for populations11
2?4?4Probability distributions for samples12
1?1What is analytical chemistry1
1?2Measurement of the analyte2
1?3Range2
1?4The analytical perspective3

2?1Determinate errors5
2?2Indeterminate errors6
2?3Accuracy and precision6
2?3?1Ways of expressing accuracy7
2?3?2Ways of expressing precision8
2?4The distribution of measurements and results9
2?4?1Populations and samples10
2?4?2Probability distributions for populations10
2?4?3Confidence intervals for populations11
2?4?4Probability distributions for samples12
2?5Confidence intervals for samples14
2?6Rejection of a result15
2?7Significant figures16
2?7?1Multiplication and division17
2?7?2Addition and subtraction18
2?7?3Logarithms19
2?8Rounding off19
本章小結20
PROBLEMS21


3?1General principles23
3?1?1Titration23
3?1?2Standard solutions23
3?1?3Classification of volumetric methods24
3?2Titer25
本章小結26



4?1Aqueous Acid?Base Theories27
4?2Acid?Base Equilbria in Water28
4?3The pH Scale29
4?3?1Proton Balance Equation30
4?3?2Weak Acids and Bases30
4?3?3Salts of Weal Acids and Bases31
4?3?4Polyprotic Acids and Their Salts32
4?3?5Buffers33
4?4Fraction of Dissociating Species at a Given pH:α?Values35
本章小結37
PROBLEMS38



5?1Strong acid strong base39
5?2Detection of the end point:indicators41
5?3Acid versus base43
5?3?1Weak acid versus strong base43
5?3?2Titration of polyprotic acid46
5?3?3Mixtures of acid or base46
5?4Preparation of standard base solutions48
5?5Preparation of standard acid solutions49
本章小結49
PROBLEMS51


6?1Complexes:formation constants53
6?2Chelates:EDTA54
6?2?1Metal?EDTA formation constants55
6?2?2EDTA is a weak acid55
6?2?3The formation constant55
6?2?4EDTA must compete with other ligands56
6?3EDTA titration curves57
6?3?1Calculating the titration curve57
6?4Detection of the end point:indicators60
6?5High purity EDTA62
6?6Fraction of dissociating species in polyligand complexes:β?values63
本章小結65
PROBLEMS66



7?1Principles67
7?2Electrochemical cells68
7?3The Nernst equation70
7?4Calculation of the equilibrium constant of a reaction72
7?5Titration curves73
7?6Detection of the end point76
7?6?1Self?indication76
7?6?2Starch indicator77
7?6?3Redox indictors77
7?7Formal potential78
7?7?1Dependence of potential on pH79
7?7?2Dependence of potential on complexation79
7?8Limitations of electrode potentials80
7?9Tetrations involving lodine:iodimetry and iodometry80
7?9?1Iodimetry80
7?9?2Iodometry82
7?10Titrations with oxidizing agents83
7?11Titration with reducing agents86
7?12Preparation of the analyte solution86
本章小結88
PROBLEMS89

8?1Effect of acidity on solubility of precipitates91
8?2Precipitation titrations93
8?2?1Titration curves93
8?2?2Detection of the end point: indicators95
本章小結98
PROBLEMS99



9?1Precipitation equilibria: the solubility product101
9?2The diverse ion effect on solubility:Ksp102
9?3Unit operations in gravimetric analysis103
9?3?1Steps of gravimetric analysis103
9?3?2Conditions for analytical precipitation104
9?3?3Digestion of the precipitate 105
9?3?4Impurities in precipitates107
9?3?5Washing and filtering the precipitates 108
9?3?6Drying or igniting the precipitate 109
9?3?7Homogeneous precipitation110
9?4Examples of gravimetric analysis111
本章小結111
PROBLEMS112



10?1What is electromagnetic radiation114
10?1?1Wave properties of electromagnetic radiation 114
10?1?2Particle properties of electromagnetic radiation115
10?2Spectroscopy based on absorption116
10?2?1Absorbance of electromagnetic radiation116
10?2?2UV/Vis spectra for molecules and ions116
10?3Transmittance and absorbance118
10?4Absorbance and concentration: Beer’s law119
10?5Beer’s law and multicomponent samples120
10?6Limitations to Beer’s law120
10?6?1Foundamental limitations to Beer’s law 120
10?6?2Chemical limitations to Beer’s law 121
10?6?3Instrumental limitations to Beer’s law121
本章小結122
PROBLEMS123



11?1Classifying separation techniques125
11?1?1Separation by precipitation125
11?1?2Extraction between two phases 127
11?1?3Liquid?liquid extractions 127
11?2Partition coefficients and distribution rations128
本章小結130



12?1Air analysis131
12?1?1Air sample collection131
12?1?2Air sample analysis134
12?2Water analysis134
12?2?1Sampling of water135
12?2?2Analysis of water samples135

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Potassium permanganate is a widely used oxidizing titrant. It acts as a self-indicatorfor end-point detection and is a very strong oxidizing agent . The solution is stable if precautions are taken in its preparation. When the solution is first prepared, small amounts of reducing impurities in the solution reduce a small amount ofthe MnO4-. In neutral solution, the reduction product of this permanganate is MnO2,rather than Mn2+ produced in acid medium. The MnO2 acts as a catalyst for further decomposition of the permanganate, which produces more MnOz, and so on. This iscalled autocatalytic decomposition. The solution can stabilized by removing theMnO2. So, before standardizing, the solution is boiled to hasten oxidation of all impurities and is allowed to stand overnight. The MnO2 is then removed by filtering through asintered-glass filter. Potassium permanganate can be standardized by titrating primarystandard sodium oxalate, Na2C2O4, which, dissolved in acid, forms oxalic acid.
The solution must be heated for rapid reaction. The reaction is catalyzed by theMn2+ product and it goes very slowly at first until some Mn2+ is formed. Pure electrolytic iron metal can also be used as the primary standard. It is dissolved in acid and reduced to Fe2+ for titration (see below, under Preparation of the Analyte Solution) .

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