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COMPARATIVE STUDY BETWEEN NEAR- INFRARED (NIR) SPECTROMETERS IN THE MEASUREMENT OF SUCROSE
CONCENTRATION
ZCT 390/6: PURE PHYSICS PROJECT
NUR FATIHA AKMA BINTI ISMAIL
109012
DR. AHMAD FAIRUZ BIN OMAR
SCHOOL OF PYHSICS
UNIVERSITI SAINS MALAYSIA
2012/2013
ACKNOWLEDGEMENT
This final year project would be impossible without the guidance and help of several
individuals. First of all, I would like to express my deep and sincere gratitude to my final year project
supervisor, Dr. Ahmad Fairuz bin Omar, Lecturer of the School of Physics, University of Science
Malaysia. He had shared a lot of his knowledge in order for my partner and me to finish our project.
He also willing to sacrifice his busy schedule to give my partner and me the guidance to complete
this thesis. His understanding, encouraging and personal guidances make me not hesitate to proceed
this project until its completion.
Besides that, my full appreciation goes to my project partner, Nurul Izati binti Azizan whose
gave me a lot of courage to finish our project in duration of two semesters. I owe for her patient with
my attitude and let her intelligence to be shared with me. She also willing to sacrifice her busy duty
task in order to discuss about our project.
On top of that, my heartfully thankful to the Engineering Lab of School of Physics assistants
who had given us permission to use the lab even during the semester break. Without their permission
and assistant, we absolutely cannot finish our project since the apparatus and materials in the
engineering lab are very important in our project.
Furthermore, I want to give my morally appreciation to my family, roommates and friends.
Without their understanding, encouragement and motivation, it is impossible for me to finish this
project. My special appreciation goes to my parents, Norzaini binti Ismail and Ismail bin Hassim for
their understanding and loving support.
On top of that, I also want to express my thanks to the School of Physics, University of
Science Malaysia because all the financial support come from them.
Finally, I would like to thanks to everybody who was involved in the process of the
completion of this project. I also want to apologize because I could not mention one by one. Thanks
a lot for the cooperation given whether on direct or indirect way.
ii
TABLE OF CONTENTS
ACKNOWLEDGEMENT ii
TABLE OF CONTENTS iii
LIST OF TABLES vi
LIST OF FIGURES vii
LIST OF ABBREVIATIONS viii
LIST OF SYMBOL ix
ABSTRAK x
ABSTRACT xi
CHAPTER 1 – INTRODUCTION
1.1 Spectroscopy 1
1.1.1 NIR Spectroscopy 2
1.1.2 Spectroscopic Properties of Aqueous Sucrose Solution 4
1.2 The importance of Calibration Transfer 5
1.3 The Importance of Measuring Sucrose in Fruit 6
1.4 Objectives 8
1.5 Proble Statement 8
1.6 Outline of Thesis 8
iii
CHAPTER 2 – LITERATURE REVIEW
2.1 Response Analysis between NIR Spectrometers 9
2.2 Application of NIR spectroscopy in Various Field 12
CHAPTER 3 – MATERIALS AND METHOD
3.1 Apparatus and Material Background 16
3.1.1 Jaz Spectrometer 16
3.1.2 QE65000 Spectrometer 19
3.1.3 NIR Quest Spectrometer 21
3.1.4 Refractometer 23
3.1.5 Sample - Sucrose 26
3.2 Experiment Setup 28
3.3 Methodology 31
iv
CHAPTER 4 – RESULTS AND DISCUSSION
4.1 Response Analysis between Jaz and QE65000 Spectrometer 34
4.2 Response Analysis of NIRQuest Spectrometer 40
4.3 Response Analysis between NIR Spectrometer 44
CHAPTER 5 – CONCLUSIONS AND RECOMMENDATIONS 46
REFERENCES 48
APPENDIX 50
v
LIST OF TABLES
Table 2.1 Summary of the linear relationship between absorbance and sucrose concentrations.
Table 3.1 Properties of Jaz Spectrometer.
Table 3.2 The Technical Properties of QE65000 spectrometer.
Table 3.4 The characteristics and properties of NIR spectrometers.
Table 3.5 Samples Characteristics.
Table 4.1 Results from MLR using Wavelengths from O-H and C-H absorbance bands for Jaz
and QE65000 spectrometer.
Table 4.2 Results from MLR using Wavelengths from O-H and C-H absorbance bands for
NIRQuest spectrometer.
vi
LIST OF FIGURES
Figure 1.1 Electromagnetic Spectrum.
Figure 1.2 An Example of NIR Absorption Spectrum of Paper.
Figure 1.3 Scatter plots between actual and NIR-predicted values for sucrose in mangoes
Figure 1.4 The example of starch test.
Figure 2.1 Linear Relationship between Absorbance and Concentration of Aqueous Sucrose at
wavelength 959 nm.
Figure 2.2 Peak shift in NIR absorbance spectra from different water-sucrose concentration.
Figure 2.3 Measured vs. predicted values of the soluble solids content (%Brix) of Jonagold apple
based on NIR reflectance spectra.
Figure 2.4 Correlation of banana sugar contents measured chemically as well as non
destructively by means of NIR spectroscopy.
Figure 3.1 The Jaz Spectrometer.
Figure 3.2 QE65000 Spectrometer.
Figure 3.3 NIRQuest512-2.2 Spectrometer.
Figure 3.4 A modern digital handheld refractometer being cleaned under a faucet.
Figure 3.5 Skeletal Formula for Sucrose.
Figure 3.6 The Formation of Sucrose from Glucose and Fructose.
Figure 3.7 Experiment Setup for NIR Measurement (Side view).
Figure 3.8 Flow chart of experiment.
Figure 4.1 Linear relationship between absorbance and concentration of aqueous sucrose at λ =
959 nm by using (a) Jaz spectrometer, and (b) QE65000 spectrometer.
Figure 4.2 Coefficient of determination generated at different wavelength for aqueous sucrose
concentration by using (a) Jaz spectrometer, and (b) QE65000 spectrometer.
vii
Figure 4.3 Calculated VS actual concentrations of sucrose by using (a) Jaz spectrometer, and (b) QE65000 spectrometer.
Figure 4.4 Coefficient of determination generated at different wavelengths for aqueous sucrose
concentration by using NIRQuest spectrometer.
Figure 4.5 Calculated VS actual concentrations of sucrose by using NIRQuestspectrometer.
viii
LIST OF ABBREVIATIONS
IR Infra-red
RMSEC Root Mean Square of Calibration model
CCD Charge-Coupled Device
DPU Data Processing Unit
FWHM Full-Width Half-Maximum
A/D Analog-to-Digital
FFT Fast Fourier Transform
OLED Organic Light- Emitting Diode
RI Refractive index
ATC Air Traffic Control
QA Quality Assurance
RDS Refractometric Dried Substance
OD Optical density
MLR Multiple Linear Regression
ix
LIST OF SYMBOLS
λ Wavelength
nm Nanometer
°Brix Degree Brix
%w/w Percentage by weight
mm Millimeter
Aλ Absorbance at wavelength λ
Sλ Sample intensity at wavelength λ
Dλ Dark intensity at wavelength λ
Rλ Reference intensity at wavelength λ
Aλ Absorbance at wavelength,
Eλ Extinction coefficient of the absorbing species at wavelength lamda,
C Concentration of the absorbing species,
l Optical path length of the absorption.
x
ABSTRAK
Pemindahan penentukuran merupakan topik yang amat penting dan hangat diperkatakan bagi
tujuan aplikasi sains dan praktikal dalam bidang spektroskopi. Tesis ini bertujuan menyiasat
pemindahan penentukuran antara spektrometer-spektrometer inframerah-dekat yang berlainan.
Antara jenis spektrometer yang digunakan di dalam penyiasatan ini adalah Jaz, QE65000, dan
inframerah-dekat. Pengukuran kandungan gula merupakan salah satu kaedah yang penting untuk
memastikan tanaman dituai pada masa yang tepat supaya buah-buah yang baik dan berkualiti dapat
dihasilkan. Sampel yang digunakan di dalam penyiasatan ini adalah sukrosa, C12H22O11, yang
dipelbagaikan kepekatannya kepada lima puluh data. Kepekatan sukrosa diukur menggunakan
refraktometer di dalam unit darjah brix (°Brix). Darjah brix merupakan kandungan gula di dalam
larutan berair. Satu darjah brix didefinisikan sebagai 1 gram sukrosa di dalam 100 gram larutan dan
mewakili kekuatan larutan menerusi peratusan berat (%w/w). Jika larutan mengandungi pepejal yang
dilarut selain daripada sukrosa tulen, maka °Brix hanya menganggarkan kandungan pepejal yang
dilarut. Pengukuran spekstroskopi di dalam kerja ini dijalankan menggunakan julat panjang
gelombang antara 650-1100 nm untuk spektrometer Jaz dan QE65000. Manakala, untuk
spektrometer NIRQuest, 900-2200 nm. Bagi spektrometer Jaz dan QE65000, panjang gelombang
pada nilai 959 nm dikenalpasti sebagai penghasil pekali penentuan, R2, yang paling tinggi antara
penyerapan dan kepekatan sukrosa dan bagi spektrometer NIRQuest, panjang gelombang
dikenalpasti pada pada nilai 1363 nm. Kombinasi antara panjang gelombang infra-merah dekat
(NIR) (ƛ=730, 830, 915, dan 960 nm) untuk spektrometer Jaz, (ƛ=909 dan 960 nm) untuk
spektrometer QE65000 , dan (ƛ=980, 1156, 1163, 1195, 1337, 1350, 1395, 1606, 1670, 1676, dan
1682 nm) untuk spektrometer NIRQuest antara lingkaran C-H dan O-H membolehkan kita
mengkuantitikan kepekatan sukrosa. Selepas kombinasi panjang gelombang dilakukan, pekali
penentuan meningkat untuk spektrometer Jaz (R2= 0.992; RMSEC = 0.907 °Brix), untuk
spektrometer QE65000 (R2= 0.995; RMSEC = 0.760 °Brix), dan untuk spektrometer NIRQuest (R2
= 0.982; RMSEC = 1.613 °Brix).
xi
ABSTRACT
The calibration transfer is a very important and popular topic in the science and practical
application of spectroscopy. In this thesis, we investigate the calibration transfer between different
types of spectrometer. The types of spectrometer used in this project are Jaz spectrometer, QE65000
spectrometer, and Near-Infrared (NIR) spectrometer. The measurement of sugars is one of the
important procedure in the determination of the right time to harvest the crops in order to obtain a
good and high quality of fruits. The sample used is sucrose, C12H22O11 with the variation of
concentration divided almost equally to fifty data. The sucrose concentration is measured by using
refractometer and the result obtained in unit of degree brix (°Brix). Degree brix is a sugar content of
an aqueous solution. One degree Brix is 1 gram of sucrose in 100 grams of solution and represents
the strength of the solution as percentage by weight (% w/w). If the solution contains dissolved
solids other than pure sucrose, then the °Brix only approximates the dissolved solid content.
Spectroscopic measurement in this work was conducted on the range of wavelength between 650-
1100 nm for Jaz and QE65000 spectrometer and 900-2200 nm for NIRQuest spectrometer. For Jaz
and QE65000 spectrometer, wavelength at 959 nm is identified as producing the highest coefficient
of determination, R2 , between absorbance and aqueous sucrose concentration (°Brix). Whereas, for
NIRQuest spectrometer, wavelength at 1363 nm is identified as producing the highest coefficient of
determination, R2 , between absorbance and aqueous sucrose concentration (°Brix). Combination of
NIR wavelengths (λ=730, 830, 915, and 960 nm), (λ=909 and 960 nm), and (λ=980, 1156, 1163,
1195, 1337, 1350, 1395, 1606, 1670, 1676, and 1682) within C-H and O-H bands can reliably
quantify sucrose by using Jaz spectrometer (R2= 0.992; RMSEC = 0.907 °Brix), QE65000
spectrometer (R2= 0.995; RMSEC = 0.760 °Brix), and NIRQuest (R2 = 0.982; RMSEC = 1.613
°Brix) respectively.
xii
CHAPTER 1
INTRODUCTION
1.1 Spectroscopy
Spectroscopy is a scientific discipline studying interactions of light with matter. Light can be
of different wavelengths, which is represented by the electromagnetic spectrum. The IR region is
roughly divided into three intervals: near, mid and far-IR. The near-IR (NIR) region covers the
wavelength range 780 - 2500 nm. Figure 1.1 shows the electromagnetic spectrum.
Absorption of light in the IR region causes molecules to vibrate and rotate. Absorption of
light in the matter is usually not uniform and depends on molecular structure. At certain intervals the
absorption is more intense, which is represented in the form of absorption bands. In NIR, the
absorption bands are related to the combination vibrations and overtones of C-H, O-H and N-H
chemical moieties in the material. Plots of absorbance vs. wavelength are called absorption spectra.
Almost each absorption spectrum is unique and spectra of slightly different materials are only
slightly different[1].
Figure 1.1 Electromagnetic Spectrum[1].
1
Spectroscopic studies were central to the development of quantum mechanics and
included Max Planck's explanation of blackbody radiation, Albert Einstein's explanation of
the photoelectric effect and Niels Bohr's explanation of atomic structure and spectra. Spectroscopy is
used in physical and analytical chemistry because atoms and molecules have unique spectra. As a
result, these spectra can be used to detect, identify and quantify information about the atoms and
molecules. Spectroscopy is also used in astronomy and remote sensing on earth. Most research
telescopes have spectrographs. The measured spectra are used to determine the chemical
composition and physical properties of astronomical objects such as their temperature and velocity.
1.1.1 NIR Spectroscopy
NIR Spectroscopy is a spectroscopic method that uses the near-infrared region of the
electromagnetic spectrum (from about 800 nm to 2500 nm). Typical applications pharmaceutical,
medical diagnostics (including blood sugar and pulse oximetry), food and agrochemical quality
control, and combustion research, as well as research in functional neuroimaging, sports medicine
and science, elite sport training, etraining, ergonomics, rehabilitation, neonatal research, brain
computer interface, neurology (neurovascular coupling)[2].
NIR spectra have only a few significant peaks, but they are exceptionally information-rich
due to the number of overlapping absorption bands. Thus, interpretation of NIR spectra is usually
combined with mathematical and statistical methods (i.e. chemometric methods) in order to extract
the necessary information.
Near-infrared spectroscopy is based on molecular overtone and combination vibrations. Such
transitions are forbidden by the selection rules of quantum mechanics. As a result, the molar
absorptivity in the near IR region is typically quite small. One advantage is that NIR can typically
penetrate much farther into a sample than mid infrared radiation. Near-infrared spectroscopy is,
therefore, not a particularly sensitive technique, but it can be very useful in probing bulk material
with little or no sample preparation.
2
Figure 1.2 An Example of NIR Absorption Spectrum of Paper [1]
The molecular overtone and combination bands seen in the near IR are typically very broad,
leading to complex spectra; it can be difficult to assign specific features to specific chemical
components. Multivariate (multiple variables) calibration techniques (e.g., principal components
analysis, partial least squares, or artificial neural networks) are often employed to extract the desired
chemical information. Careful development of a set of calibration samples and application of
multivariate calibration techniques is essential for near-infrared analytical methods.
Near Infrared (NIR) spectroscopy is used for fast, reliable, and non-destructive
measurements that simultaneously control manufacturing processes and product quality, assuring
that final product specifications and quality are met. The functionality of the product can be
determined in both a quantitative and qualitative manner, and measurements can be carried out on
solid or liquid samples. Combining a high sampling rate with a flexible optical delivery method,
Polytec-designed spectrometers utilize fiber-optic probes to fill a wide range of applications in
process control. NIR Spectroscopy – Simple and Flexible Optical spectroscopy covers wavelengths
from 200 nm to 25 µm (see Figure 1) and is divided into three important spectral ranges:
Ultraviolet/visible: 200 – 760 nm, Near Infrared : 760 – 2500 nm, Mid-Infrared : 2500 nm – 25 µm.
Photons in the Ultraviolet/Visible spectral range have enough energy to excite or ionize materials
by raising the energy level of bound electrons.
3
NIR radiation has less energy/photon but does excite molecular vibrations. Vibrational
spectroscopy in the NIR range is used for process monitoring and quality control. The NIR
wavelengths enable a very flexible measurement setup and a high measuring rate. Another advantage
of using the NIR spectral range is the low coefficient of absorbance, allowing relatively deep
penetration of the radiation in the sample. Therefore, samples can be measured without substantial
preparation and information on both surface and volume parameters can be acquired. Finally, these
measurements are non-destructive and samples are not altered and can be reused. The advantages of
NIR spectroscopy make integration into automated production processes much easier, and the
availability of fiber-coupled measuring heads allows for flexible measurement set-ups[3].
1.1.2 Spectroscopic Properties of Aqueous Sucrose Solution
In this thesis, the focus was on spectroscopic measurement of sucrose. Sucrose is a
disaccharide sugar that can be made from the combinations of glucose and fructose and has a
molecular number of C12H22O11. The determination of the amount of sugar in fruits has been
conducted a long time ago. One of the noticeable research was done by Stephen R. Delwiche, Weena
Mekwatanakarn and Chien Y. Wang. They investigate the potential of NIR spectroscopy to predict
soluble solids content (SSC) and individual and combined concentrations of sucrose, glucose, and
fructose nondestructively in mango. From their research, the result for sucrose was presented in the
figure 1.2.
Based on their research, they found that sucrose produced better PLS performance compared
to glucose and fructose for probable reasons of its greater abundance and higher correlation to SSC.
From the standpoint of NIR analysis, the relative abundance of sucrose is fortunate, considering that
sucrose is the best indicator of sweetness in mango fruit.
During fruit development, sucrose was found to accumulate the greatest amount of the carbon
released from the breakdown of starch. Therefore, sucrose concentration, and perhaps that of one or
more of the reducing sugars, could be used, along with SSC, as an indicator of ripeness. However,
determination of these constituents requires destructive methodology and, in the case of the sugars,
expensive and labor-intensive equipment. Near-infrared (NIR) spectroscopy, which is a
nondestructive method for fruit quality evaluation, has become a very popular technique and has
been used to evaluate the internal quality of many fruit[6].
4
Figure 1.3 Scatter plots between actual and NIR-predicted values for sucrose in mangoes[6].
1.2 The Importance of Calibration Transfer
Calibration transfer means that we transfer the calibration of one instrument to the another
instrument. Meaning that, both of the instruments shared the same calibration. Not only on different
instruments, calibration transfer may also applied to the experiment that using different sample of
materials. In this kind of experiment, the instrument used need to be fixed. Calibration transfer in
multivariate calibration is one of the most important and key issues in near-infrared spectral analysis
technology. The model was transferred by means of finding the transformation relation between two
instruments of the same type, so that the model established on one instrument could be used on the
other to predict the spectral response[4].
calibration transfer is a series of approaches or techniques used to attempt to apply a single
spectral database, and the calibration model developed using that database, to two or more
instruments. Calibration transfer involves several steps. The basic spectra are initially measured on at
least one instrument (parent, primary, or master instrument) and combined with the corresponding
reference chemical information (actual values) for the development of calibration models. These
models are maintained on the original instrument over time, are used to make the initial calibration,
5
and are transferred to other instruments (child, secondary, or transfer instruments). This process
enables analysis using the child instruments with minimal intervention and recalibration. We note
that the issue of calibration transfer disappears if the instruments are precisely alike. If instruments
are the "same" then one sample placed on any of the instruments will predict or report precisely the
"same" result. Because instruments are not alike, and in fact change over time, the use of calibration
transfer techniques is often applied to produce the best attempt at calibration model or data
transfer[5].
1.3 The Importance of Measuring Sugar Content in Fruit
The measurement of sugar in fruit is the important aspect to test the maturity of fruit and
obtain the right time to harvest it. In the case of most stone fruits, when the fruit has colored well and
is beginning to soften, it is ripe for picking. Some of the newerpeach and nectarine varieties have
been developed with high red color and firmer texture, making it more difficult to tell when they are
ready to pick. Taste is still a good indicator of ripeness. Sample one, and if its level of sweetness is
good even though the texture is a bit crunchy, it is probably ready. Fruits that you want to transport
or save for display should be picked firm but mature. Fruit can be placed in a box lined with
newspaper or other padding, with the stem end down. Avoid packing peaches and nectarines more
than two layers deep or the bottom layer of fruit may be damaged. In a few days the fruit will soften
and be ready to eat.
Sugar levels are a commonly used measurement in a wide range of crops. In the citrus
industry this is a measure of the total soluble solids in the juice. These soluble solids are primarily
sugars; sucrose, fructose, and glucose. As the flesh of fruit forms it deposits nutrients as starch that,
as the fruit ripens, transform to sugars. The percentage sugar, measured in degrees Brix ( oBrix),
indicates the sweetness of the fruit by measuring the number of soluble solids in the juice. Sugar
measurement is one of the step taken in maturity testing of fruit. Other than that, the result from the
sugar measurement will contribute to the calculation of sugar-acid ratio with the formula
concentration of sugar in oBrix divided by citric acid concentration. Calculation of sugar-acid
concentration is also one of the step needed in order to test the maturity of fruit.
6
The maturity testing of fruit will provide the information to the farmer the right time to
harvest the crop. The ripening of fruit is a complex procedure. Release of ethylene gas triggers whole
families of enzymes, including amylases, kinases, hydrolases and pectinases to work their magic and
neutralize acids, form anthrocyanins that give colors to fruit, and soften hard, inedible fruits into
toothsome, delicious ones. One critical element of the ripening involves the conversion of starches to
sugars. So, in order to complete the ripening process, the farmer needs to know the sugar level in the
fruit. But, certain fruit have different sugar level depends on their cluster. Usually the fruit from high
of the cluster contained more sugar than the fruit from bottom of the cluster. The fruit from clusters
exposed to the sun contain more sugar than the fruit from cluster growing in heavy shade. So,
because of the large variations in sugar content, large size samples must be collected to produce
accurate results[6].
When a sample fruit is cut horizontally through the core and sprayed with a mild iodine
solution, the iodine turns the cells containing starch dark, but does not color those cells containing
sugar. Figure 1.3 shows the starch test, which indicates visibly the stage of ripeness that a fruit has
reached. It is one of the easiest and most useful indicators available for the home orchardist. When
only the area of the core is clear of starch, and the rest is dark, the fruit is usually unripe and
immature. Fruit that we want to store should be picked when one-half to three-quarters of the sample
cross section area is clear of starch. Usually at that point it has developed enough sugar to taste good
(mature), and still retains sufficient starch to continue developing in storage (pre-climacteric). If
most of the cross section of the fruit is clear of starch, it is too ripe for long storage and should be
consumed at once or stored short-term only.
Figure 1.4 The example of starch test[7]
7
1.5 Problem Statement
The NIR spectrometers are widely used in the spectroscopy field. Calibration transfer in
multivariate calibration is one of the most important and key issues in near-infrared spectral analysis
technology. The model was transferred by means of finding the transformation relation between two
instruments of the same type, so that the model established on one instrument could be used on the
other to predict the spectral response.
The calibration transfer between NIR spectrometers should be practiced in spectroscopy field
to improve the efficiency in energy, time and work. But, in order to complete the calibration transfer
process, the response analysis on each spectrometer needs to be observed first. So, the comparative
study between NIR spectrometers need to be done in order to give the information about the
properties of each spectrometer.
1.4 Objectives
1. To compare the response analysis between lower and same range of NIR wavelength (700 – 1100 nm) by using QE65000 spectrometer with the previous research conducted by Ahmad Fairuz Omar, Hanafi Atan, and Mohd Zubir Mat Jafri, [8] by using Jaz spectrometer.
2. To identify response analysis of higher range of wavelength ( 900 – 2500 nm) by using NIRQuest spectrometer.
3. To compare response analysis between lower and higher range of NIR wavelength spectrometer.
1.6 Outline of Thesis
This thesis consists of five chapters. Chapter 1 presents the objective of study, problem
satatement regarding the study, theoretical background about spectroscopy field, the definition and
the importance of calibration transfer and the uses of measuring glucose in food industry. Chapter 2
comprises a review of relevant literature based on the past research. Chapter 3 clarify the experiment
details on the the background of the apparatus and material used, sample preparation, apparatus set
up and the procedure of the experiment conducted. Next, the results and data obtained from the
experiment conducted are discussed in chapter 4 to get the equation of calibration transfer between
NIR spectrometers in the sugar measurement. Finally, chapter 5 summarizes the main findings in this
study and concludes the thesis.
8
CHAPTER 2
LITERATURE REVIEW
2.1 Response Analysis of NIR Spectrometer on Aqueous Sucrose Solution
There are some research that has been done by using the Jaz spectrometer and sucrose. For
example the research titled Peak Response Identification through Near-Infrared Spectroscopy
Analysis on Aqueous Sucrose, Glucose, and Fructose Solution that has been done by Ahmad Fairuz
Omar, Hanafi Atan, and Mohd Zubir Mat Jafri. They used 50 set of sugar concentration for
calibration and validation. For their research, let us highlight the result on sucrose solution. Their
result shows that four wavelengths that produced the highest efficiency algorithm for sucrose are
830, 909, 960, and 965 nm. The calibration algorithm obtained are shown below:
SC = 122 + 1375λ730 - 942λ830 + 855λ915 - 736λ960 (1)
(R2= 0.992; RMSEC = 0.907 °Brix);
Where : SC is the sucrose concentration in °Brix
The linear relationship between absorbance and aqueous sucrose concentration has also
been obtained in their research as shown in the Figure 2.1. The relationship is determined at
wavelength 959 nm. The absorbance decrease as the concentration of the sucrose increase. So, we
can conclude that the absorbance is inversely proportional to the concentration of sucrose. In their
research paper, they also mentioned that from their investigation towards glucose, fructose, and
sucrose, they found that the absorbance loose its linearity once it has moved further than wavelength
960 nm.
9
Figure 2.1Linear Relationship between Absorbance and Concentration of Aqueous Sucrose at
wavelength 959 nm[8].
Before this research, Amad Fairuz Omar alone has published the other research article titled
Quantifying water-sucrose solutions through NIR spectral absorbance linearisation and gradient shift.
In this research article, we can get the information about the sucrose properties with variation of
wavelength. Two analyses have been performed in this research. The first analysis is in the
measurement of sucrose concentration through spectral absorbance linearisation. The value of
R2 between absorbance and sucrose concentration was observed to be lower for higher concentration
of sucrose, indicating that there is an improvement in spectral linearity. This observation was then
quantified to attain the value of spectral linearisation that is presented by each spectrum R2 against
the sucrose concentration. The second analysis is the quantification of sucrose concentration through
the changes of NIR spectral gradient. It was observed that from 50 absorbance spectra, for samples
with sucrose concentration between 0-35oBrix, lower NIR spectral gradient is produced for higher
sucrose concentration. This observation was then quantified by generating R2 between the spectral
gradient and sucrose concentration.
10
In order to express his result from this research, he took the research by Giangiacomo as the
reference. Giangiacomo stated that for the NIR evaluation of sucrose concentration using the range
of wavelength between 1,100 nm and 2,400 nm, the increase in sugar concentration will alter the
water band to become more symmetric and shifts the absorption peak toward longer wavelengths.
But, surprisingly, the experimental result presented in his paper which using the range of wavelength
between 900 nm and 1,100 nm does produce similar response as shown in Figure 2.2.
Figure 2.2 Peak shift in NIR absorbance spectra from different water-sucrose concentration[9].
The summary of the linear relationship between absorbance and sucrose concentration are
tabulated in Table 1. From the table, he obtained that for single wavelength analysis, 960 nm, which
is one of the absorbance peaks for water has produced the best correlation and highest accuracy of
prediction in quantifying aqueous sucrose concentration. The accuracy of measurement starts to
decay as the wavelengths moves further from 960 nm.
11
Table 1 Summary of the linear relationship between absorbance and sucrose concentrations[9].
Wavelength (nm)
R2 RMSEC Wavelength(nm)
R2 RMSEC
940 0.883 3.402 970 0.974 1.610945 0.920 2.823 975 0.963 1.927950 0.962 1.941 980 0.956 2.100955 0.976 1.546 985 0.939 2.468960 0.978 1.490 990 0.922 2.784965 0.974 1.591 995 0.894 3.240
2.2 Application of NIR Spectroscopy in Various Field
There is no research that has been done using aqueous sucrose solution together with
QE65000 spectrometer or NIRQuest spectrometer. So, in order to do the comparison between other
spectrometer, we can only analyse the properties of spectrometer itself. One of the research that used
QE65000 spectrometer has been done by Joel M. Kralj, Adam D. Douglass, Daniel R. Hochbaum,
Dougal Maclaurin, and Adam E. Cohen with the title Optical recording of action potentials in
mammalian neurons using a microbial rhodopsin. Through their research, we would like to highlight
the properties of the QE65000 spectrometer only. There is no relation with the materials they used.
The result from the spectroscopy side is the Arch and Arch(D95N) protein both had emission
maxima at 687 nm. We cannot do the prediction of our result yet because of the sample they used is
protein whereas we are using sucrose[10].
Besides that, there is also a research article that has been done by Peter Stchur, Danielle
Cleveland, Jack Zhou, and Robert G. Michel titled A Review of Recent Applications of Near-
Infrared Spectroscopy, and of The Characteristics of a Novel PbS CCD Array- Based Near-Infrared
Spectrometer. In their article, they also mentioned about the application of NIR spectrometer in the
agricultural field. A universal method for visualizing the sugar content in the flesh of melons has
been developed by Tsuta who used a CCD detector with band-pass filters. Each filter created a spatial
image of the melon sample for a specific spectral region. This method had been previously employed
for measurement of sugar distribution in green-flesh melon and kiwifruit. It was demonstrated that
the chlorophyll absorbance near 676 nm shows a strong inverse correlation with the sugar content.
However, it cannot be applied to a red-flesh melon due to the lack of chlorophyll.
12
The authors extracted a 25-mm-diameter cylindrical sample from the ‘‘equator’’ of a melon, and a
spectrum was obtained using a fiber optic probe. The wavelengths of 902 and 874 nm were used to
correlate sugar content, while the wavelengths 846 and 930nm were used to calculate the second
derivative absorbances. These two latter wavelengths were chosen because they gave the highest
correlation with sugar concentration using the least number of band-pass filters[11].
Other than that, Kerry B. Walsh, John A. Guthrie, and Justin W. Burney in their article titled
Application of commercially available, low-cost, miniaturised NIR spectrometers to the assessment
of the sugar content of intact fruit also discussed about the uses of NIR spectrometers in measuring
sugar. They developed the calibration using reflectance spectra of filter paper soaked in range of
concentrations (0–20% w/v) of sucrose, using a modified partial least squares procedure. The results
obtained are coefficient of correlation of 0.90 and 0.62, and standard error of cross-validation of 1.9
and 5.4%, respectively[12].
Next research about the NIR spectroscopy related with fruit was done by Bart M. Nicolai,
Katrien Beullens, Els Bobelyn, Ann Peirs, Wouter Saeys, Karen I. Theron, and Jeroen Lammertyn.
Their research title is Nondestructive measurement of fruit and vegetable quality by means of NIR
spectroscopy: A review. The result obtained in their research as shown in Figure 2.3. In their
research, different spectrophotometer designs and measurement principles are compared, and novel
techniques, such as time and spatially resolved spectroscopy for the estimation of light absorption
and scattering properties of vegetable tissue, as well as NIR multi- and hyperspectral imaging
techniques are reviewed.
On top of that, there is also a research that has been done by Manuela Zude titled Non-
destructive prediction of banana fruit quality using VIS/NIR spectroscopy. Since we are studying the
NIR spectroscopy, we will only highlight their result in NIR spectroscopy. Figure 2.4 shows the
result obtained in his research. The correlation coefficients of skin sugar contents and pulp sugar
contents were R2 = 0.89 for glucose, R2 = 0.41 for sucrose and R2 = 0.96 for fructose. He concluded
that internal fruit sugar contents were predicted with high accuracy using the near-infrared region of
the spectrum wavelength range. So, by using NIR spectroscopy, we can predict the maturity of the
fruit.
13
Figure 2.3 Measured vs. predicted values of the soluble solids content (%Brix) of Jonagold apple
based on NIR reflectance spectra[13].
Figure 2.4 Correlation of banana sugar contents measured chemically as well as non
destructively by means of NIR spectroscopy[14].
14
The last research is done by F.J. Rambla, S. Garrigues, and M. de la Guardia with the title
PLS-NIR determination of total sugar, glucose, fructose and sucrose in aqueous solutions of fruit
juices. The method is based on the partial least-squares (PLS) treatment of first derivative near
infrared (NIR) spectroscopic data obtained between 1200 and 2450 nm, using 1 mm pathlength cell
and a multicomponent calibration set, including seven binary mixtures and 10 ternary mixtures of
glucose, fructose and sucrose. The highlighted result is the NIR spectrum of pure water has four
intense absorbance bands at 970, 1190, 1450 and 1950 nm which reduce the wavelength range at
which absorbance measurements can be made in water solutions[15].
15
CHAPTER 3
MATERIALS AND METHOD
3.1 Apparatus and Materials Background
3.1.1 Jaz Spectrometer
Jaz is a community of stackable, modular and autonomous instruments that combine to
create the ultimate in smart sensing for lab, field and anywhere. Jaz is unfettered by the limits of
traditional optical sensing instrumentation. Its unique features and expandable platform make it
uniquely suited for field applications, remote sensing, process flow, quality assurance and more. Jaz
spectrometer is designed to incorporate a number of autonomous modules that share common
networking and electronics. Because of its modular design, high-performance spectrometer, Ethernet
connectivity, battery operation and PC-free performance, Jaz is nimble in a virtually endless array of
applications. It can be customized to include light sources, multiple channels and more.
Figure 3.1 The Jaz Spectrometer.
16
A basic Jaz includes the spectrometer module and onboard DPU. All other modules are optional, so
we can mix and match for the configuration that best handles our application. Jaz has a home in the
lab, the field, the process line and anywhere we need reliable, accurate optical sensing.
Operatingsoftware and development packages are available separately.
Choose from multiple gratings for each Jaz spectrometer channel. The choice of grating
groove density helps to determine optical resolution, spectral range and blaze wavelength. Jaz
provides a particularly compelling option for bioreflectance applications in the field, where
portability, flexibility and ease of use are critical. Jaz is a modular spectrometer-based system that
integrates into a single stack those components that otherwise would have to be handled separately:
the spectrometer, microprocessor with low-power display (in place of a PC), light source, battery
pack and even Ethernet capability for remote measurements. Reflection probes and other sampling
optics connect easily to the Jaz, keeping the overall system footprint compact and manageable[16].
Table 3.1 Properties of Jaz Spectrometer[16].
Spectrometer
Physical: 109.2 mm x 63.5 mm x 57 mm LWH; 352 g (JAZ-COMBO
only)
Detector: Sony ILX511B linear silicon CCD array (200-1100 nm)
Wavelength range: Grating dependent (extended-range grating available for
200-1025 nm coverage)
Optical resolution: ~0.3-10.0 nm FWHM
Signal-to-noise ratio: 250:1 (at full signal)
A/D resolution: signal)A/D resolution: 16 bit
Dark noise: 50 RMS counts
Dynamic range: 8.5 x 107 (system); 1300:1 for a single acquisition
Integration time: 870 μs to 65 seconds (20 s typical maximum)
Stray light: <0.05% at 600 nm; <0.10% at 435 nm
Sensitivity: 75 photons/count at 400 nm; 41 photons/count at 600 nm
Fiber optic connector: SMA 905 to 0.22 numerical aperture optical fiber
Electronics connector: 19-pin MHDMI connector; use ADP-MHDMI-RS232
adapter to interface to RS-232
17
Power options: Wall transformer (+5VDC); Power over Ethernet (Class III PoE provides 12 Watts); USB; integrated battery module(JAZ-B); Solar charger and external batteries
Inputs/Outputs: Yes, 4 onboard digital user-programmable GPIOs
OEM integration supported: Yes
Channels supported: Up to 8 spectrometers
Communications and Software
Computer interface: Onboard Blackfin® microprocessor
Operating systems: Windows XP, Vista (32/64 bit), Windows 7 (32/64 bit); OS
X and Linux when using the USB interface on PCs
Ethernet Module (optional) IEEE 802.3-compliant 10/100; includes 2 GB SD card
Industrial Communications Module(optional):
Interfaces (RS-232, RS-485); 4 analog I/O, 8 digital I/O
Trigger modes: Normal (free-running), Software, Synchronization and
External Hardware
Strobe functions: Continuous, Single, Lamp Enable
Operating software: Basic Jaz software (included) operates from DPU interface; SpectraSuite (separate purchase) acquires data from USB orEthernet connection; Overture software also available
Applications software: Irradiance measurement and other options available; application is loaded to an SD card and operates from DPU interface
Development software: Scripting program and API option for writing your own applications
Battery OptionsJAZ-B Module (optional integratedbattery):
Rechargeable Lithium-Ion; lifetime depends on number of modules (~8 hours for JAZ-COMBO only)
Rechargeable battery accessories: Lithium-Polymer solar battery, ~12 hours lifetime w/JAZ-COMBO; Lithium-Ion external battery, 21 hours lifetime w/JAZCOMBO
SD card storage: JAZ-B module includes (2) 2-GB SD cardsLight Source OptionsJAZ-UV-VIS (optional module): Deuterium-Tungsten Halogen (210-1100 nm); lifetime is
~1,500 hours (recommended for UV absorbance)JAZ-PX (optional module): Pulsed Xenon (190-1100 nm); lifetime is 4 x 108 flashes to
50% of initial intensity
18
JAZ-VIS-NIR (optional module): Tungsten Halogen (360-1100 nm); lifetime is 500-10,000 hours depending on power setting
LEDs (optional module w/replaceablebulbs):
365 nm, 405 nm, 470 nm, 590 nm, 640 nm and White wavelength options
ComplianceCE mark: Yes (all modules)RoHs: Yes (all modules)
3.1.2 QE65000 Spectrometer
The QE65000 Spectrometer is a unique combination of detector and optical bench
technologies that provides high spectral response and high optical resolution in one spectrometer
package.
The Hamamatsu FFT-CCD matrix detector used in the QE65000 provides 90% quantum
efficiency. It is a "2D" area detector that can bin a vertical row of pixels, which offers significant
improvement in the signal-to-noise ratio and signal processing speed of the detector compared with a
linear CCD, where signals are digitally added by an external circuit. In the QE65000, the 2D area
detector can better take advantage of the height of the slit and the additional light, greatly improving
system sensitivity. Because the detector in the QE65000 is back-thinned, it has great native response
in the UV and does not require the additional coatings that typically apply to other detectors for UV
applications.
The QE65000 Spectrometer is a great option for low-light level applications such as
fluorescence, Raman spectroscopy, DNA sequencing, astronomy and thin-film reflectivity. The
thermoelectric-cooled (down to -15 °C) detector features low noise and low dark signal, which
enables low-light-level detection and long integration times from 8 milliseconds to 15 minutes.
Figure 1.3 shows the QE65000 spectrometer[17].
19
Figure 3.2 QE65000 Spectrometer.
Table 3.2 The Technical Properties of QE65000 spectrometer[17].
PHYSICAL
Dimensions: 182 x 110 x 47 mm
Weight: 1.18 kg (without power supply)
DETECTOR
Detector: Hamamatsu S7031-1006 back-thinned FFT-CCD
Detector range: 200-1100 nm
Pixels: 1024 x 58; 24.6 mm square size
Pixel well depth: 300,000 electrons/well -1.5 mill. electrons/column
Sensitivity: 400 nm: 22 electrons/count, 250 nm: 26 photons/count
OPTICAL BENCH
Design: f/4, Symmetrical crossed Czerny-Turner
Focal length: 101.6 mm input, 101.6 mm output
Entrance aperture: 100 um wide slitSMA 905 to 0.22 numerical aperture single-strand fiber
SPECTROSCOPIC
Wavelength range: 200-950 nm
Optical resolution: 0.75 nm FWHM
Signal-to-noise ratio: 1000:1 (at full signal)
Dark noise: 2.5 RMS counts
Dynamic range: 25000:1 a single acquisition
Integration time: 8 milliseconds to 15 minutes
ELECTRONICS
Power consumption: 500 mA @ 5 VDC no TE cool; 3A@5 VDC with TE cool
Data transfer speed: Full spectrum to memory every 4 ms with USB 2.0 port, 8 ms with USB 1.1 port
Inputs/Outputs: 10 onboard digital user-programmable GPIOs
TEMPERATURE & THERMOELECTRIC COOLING
Temperature limits: 0 °C to 50 °C for spectrometer, no condensation
Lowest set point: 40 °C below ambient, to -15 °C
Stability: ±0.1 °C of set temperature in <2 minutes
20
3.1.3 NIRQuest Spectrometer
NIRQuest spectrometers are compact units capable of analysing the spectrum from 900 to
2500 nm. It delivers a high performance optical bench with lownoise electronics and more
customization for a wider variety of applications including medical diagnostics, pharmaceutical
analysis, environmental monitoring and process control. If we use NIR spectroscopy for research,
process or diagnostics, NIRQuest is a less costly, less complex alternative to FT-IR and comparable
technologies. Figure 3.3 shows the real picture of NIRQuest spectrometer.
Figure 3.3 NIRQuest512-2.2 Spectrometer.
One of the application of the NIRQuest spectrometer is can classify and separate 100% of
the incoming feed. This unique system allows the classification and separation of 100% of the
incoming feed. Its fast operation saves time and , helps eliminate worker intervention – making the
process fully automatic. The system analyses the whole sample from an optical sensor to obtain a
high representative result. By working in this manner, the truck classifiication and destiny decisions
reach optimum safety levels.
21
Besides that, this NIRQuest spectrometer can also be used to determine moisture, protein
and fat content. Besides the analysis to classify incoming materials, moisture, protein and fat content
of soybeans, wheat and corn can be determined. Argentina has a total grain reception average of 450
trucks per day. So, being able to classify any incoming truck in real time gives a company valuable
information. The system provides critical data such as automatic quality averages per truck and
automatic ID by sampling quickly and accurately.
The NIRQuest-512 Spectrometer's diffractive grating-based optical bench and 16-bit USB
A/D converter are conveniently mounted in the same housing. This integrated design makes the
NIRQuest512 a 182 mm x 110 mm x 47 mm small-footprint system and eliminates the need for
additional spectrometer-to-A/D converter cabling. A +5 VDC wall transformer (included) is required
to operate the system's high-performance InGaAs array detector. The NIRQuest-512 standard grating
(NIR3) provides a wavelength range of 850-1700 nm. Five other gratings are available. The usable
range is 900-1700 nm[18].
Table 4.3 The characteristics and properties of NIR spectrometers[16,17,18].
Jaz QE65000 NIRQuestCharacteristics -Modular, stackable
and autonomous components-Czemy-Turner optical bench-On-board microprocessor and OLED display-Replaceable slits and gratings-Ethemet and memory module-Battery and external memory module
-200-1100 nm spectral range-grating dependent-Resolution 0.14-7.7 nm (FWHM)-Peak quantum efficiency 90%-Back thinned 2DCCD detector-Thermoelectric cooling-6 slit options-14 grating option
-900-2050 nm spectral range-Less than 1 nm optical resolution FWHM-15000:1 signal to noise-On board thermoelectric cooling-16 bit USB A/D converter-Crossed czemy-Turner optical bench-Various trigger modesgrating options
Application -Fluorescence-Biotechnology-Raman spectroscopy-DNA sequencing-Remote sensing-Dosimetry
-Spectroscopy-Medical-Biomedical imaging analysis-Fluorescence-Luminescence detection
-Luminescence detection-Spectroscopy of emission and absorption lines spectroscopy
22
3.1.4 Refractometers
In this experiment, refractometer is used to determine the calibration value for sucrose
concentration. Refractometers work according to the principle that when a ray of light passes from
one medium to another, the speed of the light changes according to the density of the transmitting
medium. At the interface between two media, the ray changes direction as its speed suddenly
changes. This effect is known as refraction and is a familiar concept.
The refractive index (RI) of a substance is a measure of the speed of light in a substance
relative to that in a vacuum (very close to the speed in air). The RI is a physical property that
depends upon temperature and the wavelength of the light. For a particular substance the RI is a
unique number when measured using a monochromatic light source (single wavelength) at a fixed
temperature.
Handheld refractometers and bench refractometers are devices that measure the RI of a
substance, usually a liquid, but sometimes a solid. Laboratory bench refractometers utilize
monochromatic light, usually that of sodium at 589.3 nm. They also have a means for controlling
temperature or at least measuring it precisely in order to 'compensate' for any variance. A bench
refractometer can typically measure the refractive index to within 0.0001 or better. Thus, the
refractive index of water when measured with sodium light (589.3 nm) at 20 °C is 1.33299.
Scientists may wish to measure the RI when studying the physical properties of different liquids and
solids. However, bench and handheld refractometers are usually used for more pragmatic purposes,
usually to measure the concentration of a dissolved substance.
The simplest and most popular use of a bench or handheld refractometer is in measuring the
concentration of sugar in water. As the concentration of sugar increases the RI increases. A bench
or handheld refractometer can therefore be used to measure concentration of sugar provided the
relationship between RI and concentration (and temperature) is known.
The Brix scale is the most widely used scale and is based on the relationship between pure
sucrose in water concentration (weight %) and RI. The Brix scale is more popular than RI itself.
Brix is used for testing 'liquid food' products. Even when the food does not just contain sucrose in
water, but other dissolved ingredients, the Brix scale is used as a measure of 'nutritional value'. Thus
soft drinks, juices, sauces, preserves etc. are assigned 'a Brix value' as part of the Quality Assurance
for the product. Indeed, in the juice and soft drink industries, the Brix value is arguably the most
important parameter in quality control.
23
For this experiment, the refractometer used is handheld refractometer. The use of a handheld
refractometer facilitates convenient and rapid measurement of concentration in a number of liquid
and semi-solid samples. Handheld refractometers are low-cost, simple devices that are popular in a
multitude of applications. Handheld refractometers are popular because they are easy and
convenient to use and cost a fraction of a typical bench instrument. Unlike bench refractometers
handheld refractometers are limited in terms of accuracy and applicability because they utilize
natural (white) light, there is no way to control temperature and light must be transmitted by the
sample.
Using white light means that the handheld refractometer's borderline cannot be as sharp as
that obtained in a laboratory instrument. White light is made up of wavelengths from about 350 to
800 nm (the visible spectrum). Light of each wavelength travels at a different speed. This manifests
itself as blurring and coloring of the borderline. This is called dispersion (splitting into different
wavelengths). Some substances have high dispersive power and therefore will distort a 'white light'
borderline to a greater extent. This effect gets worse as the RI increases, such that some liquids may
not be measurable to an acceptable accuracy using a handheld refractometer.
The accuracy and precision is also limited by the size and optical arrangement. Typically, a
handheld refractometer can read on an RI scale to about 0.001 units, compared to a resolution of up
to 0.00001 on a bench Abbe or automatic refractometers. These values equate to about °0.2 Brix for
a handheld refractometer versus a resolution to 0.01 Brix on a bench refractometer. Accuracy on the
bench refractometer will vary according to sample type, but can be about °0.02 for a sugar solution
or soft drink, i.e. about 100 times more accurate than a handheld refractometer.
Most handheld refractometers are calibrated initially at 20 °C in the factory. When the
ambient temperature changes, the handheld refractometer temperature also changes and the
calibration is no longer valid. Certain handheld refractometers such as the Eclipse have a 'zero'
adjuster. This means the handheld refractometer can be re-set using a reliable standard such as
water. This is in fact a better way to combat changes in temperature with a handheld refractometer
than relying upon ATC. Sudden changes in temperature or applying very hot or very cold samples
(e.g. out of the refrigerator) can incur quite large errors with handheld refractometers.
24
The way to deal with this is to have good experimental technique/protocol to ensure thermal
equilibration. Because handheld refractometers work with transmitted light, highly colored or opaque
samples may not give very sharp borderlines. The position of the borderline then becomes a
subjective judgment of the user, which reduces the reproducibility of the handheld refractometer.
Automatic bench refractometers surmount this problem by measuring the reflected light from a
sample surface, rather than transmitted light. Thus, for example in the tomato paste industry,
automatic bench refractometers are considerably easier to use and much more reliable than handheld
refractometers where borderlines are often not discernible.
In spite of these limitations handheld refractometers have proven to be quite useful in practice
and many users are happy with the lower accuracy of handheld refractometers, accepting that they
provide a quick and convenient way to check their product, rather than a highly precise QA method.
Handheld refractometer food applications include the measurement of sugar in grape must
and other fresh fruit, processed food, sugar solutions and beverages. Starch, honey and salt solutions
may also be measured with handheld refractometers.
Handheld refractometers are also commonly used to control blend ratios of various industrial
liquids. Chemical blends such as glycols, battery acid, heat exchange fluids, automotive antifreeze,
aviation wing de-icing chemicals and jet fuel ice inhibitors can be controlled easily with a handheld
refractometer whilst measurement of industrial fluids such as coolants, quenchants and hydraulic oils
are also commonplace[19].
Figure 3.4 A modern digital handheld
25
3.1.5 Sample - Sucrose
Sucrose is the organic compound commonly known as table sugar and sometimes
called saccharose. A white, odorless, crystalline powder with a sweet taste, it is best known for
its nutritional role. The molecule is a disaccharide composed of the monosaccharides glucose
and fructose with the molecular formula C12H22O11. Figure 3.5 shows the formula for sucrose.
Figure 3.5 Skeletal Formula for Sucrose[20].
Sucrose is made from glucose and fructose units. Sucrose or table sugar is obtained from
sugar cane or sugar beets. The glucose and fructose units are joined by an acetal oxygen bridge in
the alpha orientation. The structure is easy to recognize because it contains the six member ring of
glucose and the five member ring of fructose. The alpha acetal is is really part of a double acetal,
since the two monosaccharides are joined at the hemiacetal of glucose and the hemiketal of the
fructose. There are no hemiacetals remaining in the sucrose and therefore sucrose is a non-reducing
sugar. Figure 3.6 shows the formation of sucrose from glucose and fructose.
Scientists and the sugar industry use degrees Brix (symbol °Bx), introduced by Adolf Brix, as
units of measurement of the mass ratio of dissolved substance to water in a liquid. A 25 °Bx sucrose
solution has 25 grams of sucrose per 100 grams of liquid; or, to put it another way, 25 grams of
sucrose sugar and 75 grams of water exist in the 100 grams of solution.
26
Figure 3.6 The Formation of Sucrose from Glucose and Fructose[21].
The Brix degrees are measured using an infrared sensor. This measurement does not equate to
Brix degrees from a density or refractive index measurement, because it will specifically measure
dissolved sugar concentration instead of all dissolved solids. When using a refractometer, one should
report the result as "refractometric dried substance" (RDS). One might speak of a liquid as having 20
°Bx RDS. This refers to a measure of percent by weight of total dried solids and, although not
technically the same as Brix degrees determined through an infrared method, renders an accurate
measurement of sucrose content, since sucrose in fact forms the majority of dried solids. The advent
of in-line infrared Brix measurement sensors has made measuring the amount of dissolved sugar in
products economical using a direct measurement[20].
27
3.2 Experiment Setup
The overall experimental setup was conducted using spectroscopic instrumentations from
Ocean Optics. The setup is illustrated in Figure 3.7. The chemical (sucrose) was diluted using pure
water (reverse osmosis) and was calibrated using PAI-I refractometer from Atago, Co.(Tokyo,
Japan) with range of measurement from 0 to 93 "Brix, resolution of 0.1 °Brix, and accuracy of +0.2
"Brix. "Brix is used (and will be used through the entire research) as the measurement unit to
standardize the unit of measurement for the entire research since it is scientifically used in
representing sugar concentration and SSC in fruits and is a conventional analytical technique for
quality monitoring in the sugar industry. In the experiment, the response was due to mixture between
water with sucrose for different type of spectrometer. This is done in order to retrieve direct
relationship between optical parameters with the chemical composition. The characteristics of
sucrose sample used in this work are listed in Table 3.3.
28
Figure 3.7 Experiment Setup for NIR Measurement (Side view).
29
Table 3.5 Sample Characteristics.
Spectrometer Range of Sucrose
(°Brix)
Mean N
(Calibration)
Jaz 0.9-35.0 17.1 50
QE65000 0.1-39.1 8.8 50
NIRQuest512-2.2 0.2-38.8 18.8 50
The value of absorbance was measured using 2 Channel Jaz Spectrometer (Channel 0: 200-
€50 nm; Channel 1: 550-1100nm), which uses Sony IIX5118 linear silicon CCD array detector with
sensitMty of up to 75 photons/count at 400nm and 47 photons/ count at 500nm. Other custom setup
prior to the experiment includes integration time: J ms, spectra averaged: 5, and boxcar smoothing: 1.
Light source used was tungsten halogen lamp with spectral emission between3S0 and 2000nm and
color temperature of 2960K. In the original representation of spectrum graph, the y-axis of the graph
is represented in the unit of counts for its intensity. Counts are the raw output data produced by the
analogue to digital converter of the spectrometer. SpectraSuite software allows this measurement to
be converted into absorbance in the unit of OD (optical density).
30
3.3 Methodology
First, the apparatus is set up and calibrated exactly as shown in Figure 3.7. The
spectrometer used is QE65000 spectrometer. Then, sucrose was diluted using pure water (reverse
osmosis) until the 39.1(°Brix) concentration aqueous sucrose is reached. It is very important to use
pure water in order to get the most accurate result. The reference spectrum was collected through an
empty quartz cuvette. Then, the concentration of aqueous sucrose in the quartz cuvette is varied until
50 data of calibration are collected. But, we need to be very careful when pour the aqueous sucrose
into the quartz cuvette because outside of it cannot keep in touch with anything especially water and
sucrose. This is because of we are using the light that passes through it. In order to allow the light to
pass the quartz cuvette without obstacle, we need to make sure that quartz cuvette always clean
without dirty.
Then, the result shown on the pc screen is saved for the purpose of analysis. All of the
above procedure are repeated for NIRQuest spectrometer. SpectraSuite uses an equation to determine
the concentration of a species in solution. The software uses this equation to evaluate each pixel on
the detector and produce the absorbance spectrum is shown in equation (2).
Aλ = - log10 {(Sλ – Dλ) / (Rλ – Dλ)} (2)
where Aλ:Absorbance at wavelength λ,
Sλ: Sample intensity at wavelength λ,
Dλ: Dark intensity at wavelength λ,
Rλ: Reference intensity at wavelength λ.
The concentration of a species in a solution directly affects the absorbance of the solution. This
relationship, known as Beer's Law, is expressed in equation (3):
Aλ = Ɛλcl (3)
31
where Aλ:Absorbance at wavelength,
Eλ:Extinction coefficient of the absorbing species at wavelength lamda,
c: Concentration of the absorbing species,
l : the optical path length of the absorption.
The performance of the calibration models and the accuracy of prediction results were evaluated
using coefficient of determination, R2, and root mean square of error, RMSE (in (°Brix), which were
calculated using Minitab (version 14) software through equation (4):
R2 = { [nΣ xy – ( Σ x) ( Σ y )] 2 } / { n Σ x2 – ( Σ x ) Г n Σ y2 - ( Σ y ) 2 ] (4)
Where n is the number of data points, and
RMSE = √ Σ ( y−Y )2/(n−1) (5)
Where Y is the predicted y values.
32
3.3.4 Flow Chart
All of the procedure taken in 3.3 are summarised in the Figure 3.8.
Figure 3.8 Flow chart of experiment.
33
Apparatus setup
Sample preparation
Collect reference spectrum
Reduce concentration of sucrose until 50 data
Save data obtained
Repeat experiment with other spectromet
er
Data analysis
CHAPTER 4
RESULTS AND DISCUSSIONS
4.1 Response Analysis between Jaz and QE65000 spectrometer
The result of Jaz spectrometer on aqueous sucrose is taken from the research article by
Ahmad Fairuz Omar, Hanafi Atan, and Mohd Zubir Mat Jafri as a reference[8]. Their result of the
research is already stated in the literature review.
Experiment was conducted for calibration process only. Significant results were managed
to be located at wavelength between approximately 940 and 985 nm. Therefore, detail analysis was
performed within this range of wavelength for Jaz and QE65000 spectrometer. Figure 4.1 shows the
resultant linear regression generated between absorbance and sucrose concentration by using Jaz and
QE65000 spectrometer and their data are tabulated in Appendix A. Wavelengths of 959 nm and 950
nm managed to generate the highest coefficient of determination and lowest RMSE for sucrose by
using Jaz spectrometer (R2 = 0.9794; RMSE = 1.43) and QE65000 spectrometer (R2 = 0.956 ; RMSE
= 2.15) respectively. From Figure 4.1, we can summarize that absorption of a specific range of NIR
wavelength decreases linearly with the increases of sucrose concentration. Higher °Brix means
higher concentration of percentage of sugar content per amount of water. Therefore, we expected that
the lower absorbance of NIR in this case would caused by the less percentage of water in the sample
compared to the increment of sugar concentration.
The pattern behaviour of linear relationship between absorbance and the sucrose
concentration against wavelengths for Jaz and QE65000 spectrometer is shown in Figure 4.2. Their
data are tabulated in the Appendix B. It can be seen that the correlation between absorbance and
sucrose concentration starts to loose its linearity once it has moved further than 960 nm. This pattern
of response is very useful for future development of a specialized optical instrument for the
measurement of SSC in fruits where an application of a single-pixel detector with specific
wavelength responsivity is required. The most common photo detectors available in the market are
those with peak sensitivity approximately between 850 and 960 nm. Therefore, from this result, the
development of a high-sensitivity single-pixel measurement system for quantifying water-sucrose
concentration is possible.
34
(a)
(b)
Figure 4.1 Linear relationship between absorbance and concentration of aqueous sucrose at λ =
959 nm by using (a) Jaz spectrometer[8], and (b) QE65000 spectrometer.
Sucrose Concentration (Brix)
Abs
orba
nce
403020100
0.12
0.11
0.10
0.09
0.08
0.07
y = -0.001394x + 0.1193; R-Sq = 0.9794
Sugars concentration (Brix)
Abs
orba
nce
403020100
0.165
0.160
0.155
0.150
0.145
0.140
0.135
0.130
y = - 0.000714x + 0.1645
35
(a)
(b)
Figure 4.2 Coefficient of determination generated at different wavelength for aqueous sucrose
concentration by using (a) Jaz spectrometer[8], and (b) QE65000 spectrometer.
36
Further analysis through the application of Multiple Linear Regression (MLR) was
conducted to the aqueous sucrose absorbance data using the combination of O-H (960 nm) and C-H
(909-915 nm) absorbance bands wavelengths. This combination has successfully improved the
correlation for sucrose measurement. The results of these analyses are tabulated in Table 4.1.
Table 4.1 Results from MLR using Wavelengths from O-H and C-H absorbance bands for Jaz and
QE65000 spectrometer.
Wavelengths
(nm)
Spectrometer
Jaz spectrometer QE65000
R2 RMSE R2 RMSE
909, 960 0.988 1.085 0.995 0.760
910, 960 0.987 1.152 0.994 0.797
910, 965 0.985 1.247 0.992 0.896
912, 960 0.988 1.081 0.993 0.907
915, 960 0.989 1.067 0.993 0.861
730, 915, 960 0.990 1.008 0.993 0.863
830, 915, 960 0.990 1.008 0.993 0.916
730, 909, 960 0.752 0.995
830, 909, 960 0.769 0.995
730, 912, 960 0.916 0.992
830, 912, 960 0.916 0.992
730, 830, 915, 960 0.992 0.907 0.865 3.80
830, 909, 960, 965 0.776 0.995
730, 912, 960, 965 0.909 0.993
37
The highest efficiency algorithm has been identified by using different wavelengths: 730, 830, 915,
and 960 nm for Jaz spectrometer, and 909 and 960 nm for QE65000 spectrometer. The calibration
algorithm, R2, and RMSE for calibration (RMSEC) are shown in equation (1) and (2). Equation (1)
was taken from literature review[8].
For Jaz spectrometer:
SC = 122 + 1375λ730 - 942λ830 + 855λ915 - 736λ960 (1)
(R2= 0.992; RMSEC = 0.907 °Brix);
For QE65000 spectrometer:
Sucrose concentration (°Brix) = 135 + 777λ909 - 824λ960 (6)
(R2= 0.995; RMSEC = 0.760 °Brix)
Where SC is the sucrose concentration in °Brix.
The linearity of the calculated models is illustrated by Figure 4.3 and their data are tabulated in
Appendix C(1) and C(2) for Jaz and QE65000 spectrometer respectively.
38
(a)
(b)
Figure 4.3 Calculated VS actual concentrations of sucrose by using (a) Jaz spectrometer[8], and (b) QE65000 spectrometer.
39
Actual Concentration (Brix)
Cal
cula
ted
Con
cent
rati
on (
Bri
x)
35302520151050
35
30
25
20
15
10
5
0
Actual Concentration (Brix)
Cal
cula
ted
Con
cent
rati
on (
Bri
x)
4035302520151050
40
35
30
25
20
15
10
5
0
4.2 Response Analysis of NIRQuest Spectrometer
Significant result is managed to be located at wavelength between approximately 980 and
1700 nm. Therefore, detail analysis was performed within this range of wavelength for NIRQuest
spectrometer. The relationship between absorbance and sucrose concentration at wavelength 1363
nm is tabulated in Appendix A.Wavelength of 1363 nm managed to generate the highest coefficient
of determination and lowest RMSE for sucrose by using NIRQuest spectrometer (R2 = 0.813; RMSE
= 4.64). From the data, we can summarize that absorption of a specific range of NIR wavelength
decreases linearly with the increases of sucrose concentration. Higher °Brix means higher
concentration of percentage of sugar content per amount of water. Therefore, we expected that the
lower absorbance of NIR in this case would caused by the less percentage of water in the sample
compared to the increment of sugar concentration.
The pattern behaviour of linear relationship between absorbance and the sucrose
concentration against wavelengths for NIRQuest spectrometer is shown in Figure 4.4 and its data is
tabulated in the Appendix B. It can be seen that the correlation between absorbance and sucrose
concentration starts to loose its linearity once it has moved further than 1400 nm. This pattern of
response is very useful for future development of a specialized optical instrument for the
measurement of SSC in fruits where an application of a single-pixel detector with specific
wavelength responsivity is required.
40
Figure 4.4 Coefficient of determination generated at different wavelengths for aqueous sucrose
concentration by using NIRQuest spectrometer.
41
Further analysis through the application of Multiple Linear Regression (MLR) was
conducted to the aqueous sucrose absorbance data using the combination of absorbance bands
wavelengths. This combination has successfully improved the correlation for sucrose measurement.
The results of these analyses are tabulated in Table 4.2.
Table 4.2 Results from MLR using Wavelengths from O-H and C-H absorbance bands for
NIRQuest spectrometer
Wavelengths
(nm)
NIR Quest
R2 RMSE
980, 1682 0.829 4.482
1156, 1682 0.780 5.090
1163, 1670 0.799 4.865
1195, 1606 0.845 4.266
1337, 1350, 1395 0.847 4.294
980, 1350, 1682 0.841 4.370
1156, 1395, 1676 0.821 4.643
1162, 1337, 1670 0.804 4.852
980, 1195, 1395, 1676 0.827 4.609
1156, 1350, 1606, 1682 0.830 4.575
1162, 1337, 1395, 1669 0.834 4.516
980, 1156, 1337, 1676, 1682 0.889 3.732
1163, 1195, 1350, 1606, 1670 0.871 4.018
1156, 1163, 1337, 1395, 1606 0.933 2.898
980, 1195, 1350, 1670, 1676 0.857 4.241
980, 1163, 1337, 1395, 1682 0.863 4.156
980, 1163, 1337, 1395, 1670, 1682 0.882 3.889
1156, 1195, 1337, 1350, 1606, 1676 0.976 1.760
980, 1156, 1163, 1195, 1337, 1350, 1395, 1606, 1670, 1676 0.981 1.637
980, 1156, 1163, 1195, 1337, 1350, 1395, 1606, 1670, 1676, 1682 0.982 1.613
42
The highest efficiency algorithm has been identified by using different wavelengths: 980, 1156,
1163, 1195, 1337, 1350, 1395, 1606, 1670, 1676, and 1682 nm. The following are the calibration
algorithm, R2, and RMSE for calibration (RMSEC):
SC = 171 + 79λ980 + 2909λ1156 - 1550λ1163 - 422λ1195 (7)
+ 445λ1337 - 1783λ1350 + 310λ1395 – 41.8λ1606 + 298λ1670 - 298λ1676 + 195λ1682
(R2 = 0.982; RMSEC = 1.613 °Brix)
Where SC is the sucrose concentration in °Brix.
The linearity of the calculated model is illustrated by Figure 4.6 and its data is tabulated in the Appendix C(3).
Actual Concentration (Brix)
Cal
cula
ted
Con
cent
rati
on (
Bri
x)
403020100
40
30
20
10
0
Figure 4.5 Calculated VS actual concentrations of sucrose by using NIRQuestspectrometer.
43
4.3 Response Analysis between NIR Spectrometers
Now, we are comparing all of the NIR spectrometers that we used in the experiment.
They are divided into small and large range of NIR that is 650-1100 nm and 900-2200 nm
respectively. By comparing the results presented in this paper and those conducted by Ahmad Fairuz
Omar, Hanafi Atan and Mohd Zubir Mat Jafri, it is observed that the results obtained by their Jaz
spectrometer for sucrose is quite alike with QE65000 spectrometer. All of the behaviour are the same
except the numerical value because they are actually from the same range of wavelength. This will
develop a calibration transfer between Jaz and QE65000 spectrometer. But, to do calibration transfer,
a validation data need to be considered in order to get the most accurate result.
Then, by comparing higher NIR wavelength and lower NIR wavelength spectrometer, it is
observed that the results obtained by conducting measurement at higher wavelength (900-2200 nm)
has also managed to produce a very useful measurement of individual sucrose concentration. It is
obviously seen that the range of absorbance in Figure 4.5 managed to produce higher responsivity.
This is because the stronger absorbance for water and other organic composition is located at the
range NIR wavelength. The combination of wavelengths using C-H and O-H bands through the
application of MLR has significantly improved the calibration model through the increase in
efficiency calibration algorithm.
The presence of water, which also absorbs strongly in the near infra-red has limited the
use of NIRs for assessment of quality of fresh produce. The NIRS technology can be applied to the
sorting of fruit at commercial packline speeds. Indeed, it is in commercial use in Japan, primarily for
melons and citrus fruit. The Japanese firms are currently marketing NIR based sorting and grading
systems for use with citrus, pome fruits and stone fruits in Japan. It is perhaps not surprising that the
technology has been applied quickly in Japan, where fruit are with huge price (single melons selling
for routinely at $30). However, with modification and reduction of price, the technology is
applicable to markets with less reward for premium quality.
44
There are some of the applications of NIR spectroscopy that have been investigated. In the
quality attribution, NIR spectroscopy can be applied to fruits such as Macadamia kernel, citrus,
pineapples, mangoes, strawberries, melons, and stone fruit. In the form of moisture determination, it
can be applied to coal. To sweet corn, NIR spectroscopy will be applied for insect damage and insect
detection. In the future, we should expect to see the application of NIR technology to assessing a
range of food products for various aspects of quality and safety.
45
CHAPTER 5
CONCLUSIONS AND RECOMMENDATIONS
This study managed to quantify the concentration of sucrose solution through the application
of NIR spectroscopy between lower range of NIR wavelength and higher range of NIR
wavelength. For a single-wavelength application, the peak absorbance was identified occur at
wavelength 959 nm for both Jaz and QE65000 spectrometer, and 1363 nm for NIRQuest
spectrometer. This result is mainly due to absorbance of water content in the solutions. From the
application of MLR, by including the absorbance band for carbohydrate, we found that the value
of R2 significantly improved with lower RMSE. The best results were generated by selections of
wavelengths with combination of NIR wavelengths (λ=730, 830, 915, and 960 nm), (λ=909 and
960 nm), and (λ=980, 1156, 1163, 1195, 1337, 1350, 1395, 1606, 1670, 1676, and 1682) within
C-H and O-H bands can reliably quantify sucrose by using Jaz spectrometer (R2= 0.992; RMSEC
= 0.907 °Brix), QE65000 spectrometer (R2= 0.995; RMSEC = 0.760 °Brix), and NIRQuest (R2 =
0.982; RMSEC = 1.613 °Brix) respectively. These wavelengths exert an important combination
in development of calibration algorithm for individual spectrometer measurement. By comparing
the three spectrometers, all of them show the same properties. There are the absorption of a
specific range of NIR wavelength decreases linearly with the increases of sucrose concentration
and further analysis through MLR has successfully improved the correlation for sucrose
measurement. Table 5.1 summarizes the comparative study between NIR spectrometers. For
future experiment, the validation data need to be recorded since it will confirm the prediction
analysis. Besides that, for more challenging experiment, the application of NIR spectroscopy to
determine fruit quality need to be practiced. So, we will be able to improve the fruit quality.
46
Type of NIR
Spectrometer
Single Wavelength
that Generates the
Highest Coefficient of
Determination
Combination of
Wavelengths that
Generate the Highest
Coefficient of
Determination
Observation from
Graphs and Data
Jaz Spectrometer 959 nm
R2 = 0.9794
RMSE = 1.43
λ=730, 830, 915, and
960 nm
R2= 0.992
RMSE = 0.907 °Brix
*The absorption of a
specific range of NIR
wavelength decreases
linearly with the
increases of sucrose
concentration.
* Further analysis
through MLR has
successfully improved
the correlation for
sucrose measurement.
QE65000 Spectrometer 959 nm
R2 = 0.956
RMSE = 2.15
λ=909 and 960 nm
R2= 0.995
RMSE = 0.760
NIRQuest
Spectrometer
1363 nm
R2 = 0.813
RMSE = 4.64
λ=980, 1156, 1163,
1195, 1337, 1350,
1395, 1606, 1670,
1676, and 1682 nm
R2 = 0.982
RMSE = 1.613
47
REFERENCES
1. SurveNIR: Near-Infrared (NIR) Spectroscopy. http://www.science4heritage.org (accessed
02.05.2013).
2. Wikipedia the Free Encyclopedia: Near-Infrared (NIR) Spectroscopy. http://en.wikipedia.org
(accessed 02.05.2013.
3. Process Control using NIR Spectroscopy. Polytec GmbH Analytics Application Note
Spectroscopy November 2007, 1-4.
4. Li QB; Zhang GJ; Xu KX; Wang Y., Application of DS algorithm to the calibration transfer
in near-infrared spectroscopy. US National Library of Medicine National Institutes of Health
2007.
5. Jerome Workman; Jr.; Howard Mark, Calibration Transfer, Part II: The Instrumentation
Aspects. Spectroscopy 2013, 28(S5), 12-25.
6. Lum Eisenman, Harvest Decision. Harvest 1999.
7. Gary Moulton; Jacky King, Tree Fruit Harvest and Storage Tips. Washington State
University Extension.
8. Ahmad Fairuz Omar; Hanafi Atan; Mohd Zubir Mat Jafri, Peak Response Identification
through Near-Infrared Spectroscopy Analysis on Aqueous Sucrose, Glucose, and Fructose
Solution. An International Journal for Rapid Communication 2012, 45:3, 190-201.
9. Ahmad Fairuz Omar, Quantifying water-sucrose solutions through NIR spectral absorbance
linearisation and gradient shift. Journal of Optics 2012.
10. Kalj JM; Douglass AD; Hochbaum DR; Maclaurin D; Cohen AE, Optical recording of action
potentials in mammalian neurons using a microbial rhodopsin. US National Library of
Medicine National Institutes of Health, 2011, 9(1):90-5.
11. Peter Stchur; Danielle Cleveland; Jack Zhou; Robert G. Michel, Review OF Recent
Applications of Near-Infrared Spectroscopy, and of the Characteristics of a Novel Pbs CCD
Array-Based Near-Infrared Spectrometer. Applied Spectroscopic Reviews, 2013, 37-41.
12. Kerry B. Walsh; John A. Guthrie; Justin W. Burney, Application of Commercially Available,
Low-Cost, Miniaturised NIR Spectrometers to the Assessment of the Sugar Content of Intact
Fruit. Australian Journal of Plant Physiology, 2000, 27(12), 1175-1186.
48
13. Bart M. Nicolai; Katrien Beullens; Els Bobelyn; Ann Peirs; Wouter Saeys; Karen l. Theron;
Jeroen Lammertyn, Nondestructive Measurement of Fruit and Vegetable Quality by Means of
NIR Spectroscopy: A Review. Postharvest Biology and Technology, 2007, 46(2), 99-118.
14. Manuela Zude, Non-Destructive Prediction of Banana Fruit Quality using VIS/NIR
Spectroscopy. Fruits, 2003, 58, 153-142.
15. F.J. Rambla; S.Garrigues; M. De la Guardia, PLS-NIR determination of total sugar, glucose,
fructose and sucrose in aqueous solutions of fruit juices. Analytica Chimica Acta, 1997,
344(1-2), 41-53.
16. Jaz Modular Spectroscopy. Jaz, 61-78.
17. Spectrometer QE-65000. The Laboratory of Analytical Opt0chemotronics, 2010.
18. NIRQuest NIR Spectrometers Data Sheet. Ocean Optics, 1-50.
19. Global Water: Handheld Refractometer Overview. http://www.globalw.com (accessed
27.05.2013)
20. Wikipedia the Free Encyclopedia: Sucrose. http://en.wikipedia.org (accessed 27.05.2013)
21. Charles E. Ophardt, Sucrose. Virtual Chembook Elmhurst College, 2003.
49
APPENDIX
A. Relationship between Absorbance and Concentration of Aqueous Sucrose for different NIR Spectrometers
A (NIRQuest) C (NIRQuest) C (QE65000) A (QE65000) C (JAZ) A (JAZ)0.191 38.8 39.1 0.136 35.0 0.0690.217 37.8 37.8 0.143 35.0 0.0710.203 36.7 38.0 0.148 30.0 0.0810.206 35.1 36.8 0.154 34.2 0.0710.207 34.1 35.7 0.151 28.2 0.0800.209 33.1 34.5 0.152 30.6 0.0810.209 32.1 34.9 0.152 28.7 0.0780.208 31.0 32.1 0.154 22.1 0.0900.217 30.0 33.2 0.156 24.4 0.0860.210 29.5 30.3 0.159 26.4 0.0790.215 28.1 31.0 0.161 30.5 0.0760.212 27.2 28.8 0.158 25.7 0.0820.220 26.4 29.2 0.158 21.8 0.0890.215 25.4 26.4 0.161 19.4 0.0930.214 24.5 27.3 0.163 15.9 0.0970.222 23.6 25.6 0.163 10.9 0.1060.219 22.5 23.9 0.165 15.2 0.0980.225 21.7 24.2 0.164 15.0 0.1010.221 20.5 24.9 0.164 12.7 0.1020.317 23.5 22.9 0.164 10.8 0.1050.321 23.0 21.8 0.164 10.1 0.1040.314 22.5 21.0 0.165 8.3 0.1090.322 21.5 20.3 0.165 8.1 0.1090.318 20.9 19.4 0.165 13.9 0.1020.331 20.1 18.4 0.167 7.1 0.1090.322 19.4 17.7 0.166 6.1 0.1100.331 18.7 16.8 0.167 10.9 0.1020.326 17.7 16.1 0.165 9.0 0.1050.324 16.4 15.2 0.166 7.5 0.1060.668 15.4 14.6 0.167 6.8 0.1120.324 14.6 13.5 0.167 5.7 0.1140.326 13.8 13.0 0.167 4.7 0.1150.327 12.2 12.1 0.168 3.5 0.1130.340 11.5 11.6 0.167 2.5 0.1150.324 10.6 10.6 0.168 1.4 0.1150.328 9.8 10.1 0.168 0.9 0.1130.326 9.0 9.3 0.168 9.6 0.1070.332 8.4 8.2 0.167 21.4 0.0890.329 7.8 7.5 0.167 14.9 0.100
50
0.333 6.7 6.7 0.167 12.9 0.1010.329 6.0 6.0 0.168 27.4 0.0810.327 5.4 5.0 0.167 35.4 0.0680.328 4.7 4.1 0.167 27.3 0.0780.333 3.6 3.8 0.167 23.8 0.0840.333 3.1 2.8 0.166 21.1 0.0890.329 2.0 2.3 0.167 17.7 0.0940.334 1.2 1.4 0.167 15.4 0.0990.331 0.2 1.0 0.167 19.4 0.0910.324 13.1 0.6 0.168 16.1 0.1020.324 17.1 0.1 0.169 11.7 0.104
B. Relationship between Wavelength and Coefficient of Determination for Different NIR Spectrometers
Wavelength (JAZ)
R2
(JAZ)Wavelength (QE65000)
R2
(QE65000)Wavelength (NIRQuest)
R2
(NIRQuest)919.99 0.353 920.19 0.874887 1050 0.442930.01 0.664 930.42 0.720742 1150 0.696939.99 0.883 939.90 0.015044 1350 0.784949.91 0.962 950.09 0.900768 1250 0.442960.11 0.978 960.27 0.951000 1450 0.451970.26 0.970 969.70 0.900147 1363 0.125980.03 0.956 979.85 0.610916990.06 0.922 989.97 0.0181761000.04 0.864 1000.08 0.475360
959.13 0.956000
51
C. The Relationship between Actual Concentration and Calculated Concentration for different NIR Spectrometers
1. JAZ Sectrometer:
C 730.08 830.12 960.11 914.9635.0 -0.039 -0.059 0.073 -0.04135.0 -0.038 -0.058 0.075 -0.03830.0 -0.037 -0.056 0.086 -0.03734.2 -0.039 -0.059 0.076 -0.03928.2 -0.038 -0.057 0.085 -0.03930.6 -0.037 -0.055 0.085 -0.03528.7 -0.039 -0.060 0.083 -0.04122.1 -0.038 -0.057 0.096 -0.03824.4 -0.037 -0.057 0.092 -0.03826.4 -0.040 -0.061 0.083 -0.04330.5 -0.038 -0.057 0.081 -0.03825.7 -0.038 -0.058 0.087 -0.03921.8 -0.038 -0.056 0.094 -0.03819.4 -0.038 -0.056 0.096 -0.03815.9 -0.038 -0.056 0.101 -0.03810.9 -0.036 -0.052 0.111 -0.03415.2 -0.037 -0.056 0.103 -0.03815.0 -0.037 -0.054 0.105 -0.03512.7 -0.037 -0.054 0.106 -0.03610.8 -0.037 -0.054 0.108 -0.03710.1 -0.037 -0.055 0.109 -0.0388.3 -0.037 -0.054 0.112 -0.0368.1 -0.036 -0.052 0.113 -0.03513.9 -0.037 -0.054 0.107 -0.0367.1 -0.037 -0.055 0.114 -0.0376.1 -0.037 -0.055 0.114 -0.03810.9 -0.038 -0.056 0.105 -0.0399.0 -0.037 -0.055 0.109 -0.0387.5 -0.037 -0.055 0.111 -0.0376.8 -0.036 -0.052 0.115 -0.0345.7 -0.036 -0.052 0.119 -0.0344.7 -0.036 -0.053 0.118 -0.0353.5 -0.037 -0.055 0.118 -0.0372.5 -0.037 -0.054 0.119 -0.0361.4 -0.037 -0.054 0.120 -0.0360.9 -0.037 -0.054 0.118 -0.0389.6 -0.036 -0.053 0.112 -0.03521.4 -0.038 -0.056 0.092 -0.03814.9 -0.036 -0.053 0.105 -0.034
52
12.9 -0.037 -0.055 0.105 -0.03727.4 -0.038 -0.056 0.085 -0.03735.4 -0.038 -0.056 0.073 -0.03627.3 -0.039 -0.057 0.082 -0.03923.8 -0.038 -0.057 0.088 -0.03921.1 -0.038 -0.056 0.094 -0.03817.7 -0.038 -0.056 0.098 -0.03815.4 -0.037 -0.054 0.102 -0.03619.4 -0.038 -0.056 0.095 -0.03816.1 -0.035 -0.051 0.106 -0.03211.7 -0.037 -0.054 0.108 -0.036
2. QE65000 Spectrometer:
C 909.21 960.2739.1 0.022 0.13637.8 0.025 0.14338.0 0.028 0.14836.8 0.026 0.15435.7 0.019 0.15134.5 0.015 0.15234.9 0.013 0.15232.1 0.013 0.15433.2 0.013 0.15630.3 0.014 0.15931.0 0.015 0.16128.8 0.011 0.15829.2 0.010 0.15826.4 0.011 0.16127.3 0.012 0.16325.6 0.010 0.16323.9 0.012 0.16524.2 0.010 0.16424.9 0.010 0.16422.9 0.009 0.16421.8 0.009 0.16421.0 0.007 0.16520.3 0.007 0.16519.4 0.007 0.16518.4 0.009 0.16717.7 0.008 0.16616.8 0.008 0.16716.1 0.006 0.16515.2 0.007 0.166
53
14.6 0.006 0.16713.5 0.006 0.16713.0 0.006 0.16712.1 0.006 0.16811.6 0.006 0.16710.6 0.007 0.16810.1 0.006 0.1689.3 0.006 0.1688.2 0.005 0.1677.5 0.005 0.1676.7 0.005 0.1676.0 0.006 0.1685.0 0.005 0.1674.1 0.005 0.1673.8 0.005 0.1672.8 0.004 0.1662.3 0.005 0.1671.4 0.005 0.1671.0 0.005 0.1670.6 0.004 0.1680.1 0.003 0.169
54
3. NIRQuest Spectrometer:
C 980.11 1156.15 1162.64 1195.06 1337.1338.8 0.0757160 0.157709 0.172617 0.209886 0.31581037.8 0.0859160 0.167909 0.182424 0.219694 0.32757936.7 0.0812083 0.163594 0.178109 0.214986 0.32404935.1 0.0812083 0.165555 0.180463 0.214986 0.32797234.1 0.0831699 0.166340 0.180855 0.216948 0.32954133.1 0.0831699 0.167909 0.182817 0.216556 0.33189532.1 0.0835622 0.168694 0.183209 0.217732 0.33346431.0 0.0835622 0.168694 0.183209 0.218125 0.33464130.0 0.0816006 0.172617 0.187132 0.217340 0.33934929.5 0.0851314 0.170263 0.185171 0.220871 0.33778028.1 0.0831699 0.173401 0.187917 0.218125 0.34170327.2 0.0851314 0.173009 0.187917 0.220479 0.34131026.4 0.0827776 0.176148 0.190663 0.219302 0.34484125.4 0.0867007 0.174578 0.189094 0.221656 0.34444924.5 0.0843468 0.174971 0.189094 0.220479 0.34562623.6 0.0847391 0.178501 0.193409 0.220086 0.34994122.5 0.0874853 0.178109 0.192625 0.223225 0.35072621.7 0.0870930 0.181248 0.195371 0.222440 0.35425720.5 0.0882699 0.180463 0.194586 0.225186 0.355434
C 1350 1394.99 1606.04 1669.68 1676.0438.8 0.367595 0.467634 0.87407 0.839937 0.83719137.8 0.378972 0.479011 0.90428 0.863476 0.86543736.7 0.375834 0.474304 0.90428 0.862299 0.86543735.1 0.379757 0.474304 0.90428 0.869753 0.86975334.1 0.380934 0.475873 0.90781 0.871714 0.87210733.1 0.383680 0.475873 0.90820 0.863084 0.86386832.1 0.385641 0.475873 0.90271 0.860337 0.85955331.0 0.386426 0.477050 0.89761 0.864260 0.86426030.0 0.390741 0.475873 0.90938 0.861122 0.86112229.5 0.389172 0.478619 0.90467 0.862691 0.86504528.1 0.393488 0.477050 0.91134 0.872891 0.87249927.2 0.393095 0.479796 0.92350 0.864653 0.86386826.4 0.397018 0.477442 0.90741 0.867791 0.86347625.4 0.396626 0.479404 0.90467 0.865437 0.86543724.5 0.397411 0.478227 0.91134 0.868576 0.86818423.6 0.401726 0.477834 0.91016 0.870930 0.87249922.5 0.402118 0.480581 0.91722 0.878776 0.87877621.7 0.405649 0.479011 0.92585 0.869753 0.87328420.5 0.406826 0.481365 0.91997 0.891330 0.890938
55
C 980.11 1156.15 1162.64 1195.06 1337.1323.5 0.0890545 0.214202 0.227540 0.224009 0.38407223.0 0.0874853 0.216163 0.229894 0.218517 0.38642622.5 0.0874853 0.214202 0.227540 0.221656 0.38407221.5 0.0851314 0.217340 0.230679 0.215771 0.38838820.9 0.0886622 0.216556 0.229502 0.218517 0.38760320.1 0.0898392 0.221263 0.234209 0.220871 0.39270319.4 0.0867007 0.218909 0.231856 0.218517 0.39074118.7 0.0863084 0.222440 0.235386 0.217340 0.39427217.7 0.0890545 0.220871 0.234209 0.219302 0.39348816.4 0.0874853 0.221263 0.234209 0.218517 0.39466515.4 0.0929776 0.251863 0.251079 0.222440 0.51118114.6 0.0933699 0.222048 0.234994 0.222832 0.39701813.8 0.0929776 0.223225 0.236171 0.223225 0.39858812.2 0.0925853 0.224794 0.237740 0.224009 0.40054911.5 0.0898392 0.229894 0.242448 0.220479 0.40525710.6 0.0906238 0.224402 0.237348 0.221263 0.4005499.8 0.0910161 0.226363 0.239310 0.222048 0.4025119.0 0.0906238 0.225971 0.238525 0.222440 0.4025118.4 0.0894468 0.227933 0.240486 0.220479 0.4048657.8 0.0969007 0.227148 0.240094 0.228325 0.4044726.7 0.0906238 0.229894 0.242448 0.222440 0.407219
C 1350 1394.99 1606.04 1669.68 1676.0423.5 0.437034 0.481758 0.94311 0.856022 0.85092223.0 0.439388 0.482150 0.95842 0.853668 0.85170722.5 0.437426 0.484504 0.96116 0.847783 0.84896021.5 0.441742 0.480188 0.95449 0.854453 0.85288320.9 0.440957 0.482542 0.95724 0.847783 0.84464520.1 0.446842 0.484111 0.95724 0.849353 0.84778319.4 0.444096 0.481365 0.95724 0.845037 0.84229118.7 0.447627 0.480581 0.95332 0.839545 0.83915317.7 0.446842 0.482150 0.96587 0.841899 0.83915316.4 0.448411 0.480973 0.96155 0.835230 0.83052215.4 0.506081 0.486858 1.00000 0.786191 0.78462114.6 0.450373 0.486073 0.98117 0.840330 0.83797613.8 0.451942 0.484896 0.97215 0.839153 0.83679912.2 0.452727 0.485288 0.95606 0.830914 0.82738311.5 0.458219 0.482542 0.95842 0.827776 0.82934510.6 0.453511 0.482934 0.97450 0.827776 0.8273839.8 0.454688 0.484896 0.97528 0.826599 0.8234609.0 0.454688 0.485288 0.97175 0.820714 0.8195378.4 0.457434 0.482934 0.98705 0.822283 0.8199297.8 0.457434 0.490781 0.99490 0.825814 0.8254226.7 0.459396 0.483719 0.98784 0.825814 0.822283
56
C 980.11 1156.15 1162.64 1195.06 1337.136.0 0.0945469 0.228717 0.241663 0.226756 0.4064345.4 0.0914084 0.227540 0.240486 0.222440 0.4060424.7 0.0902315 0.228717 0.241271 0.222048 0.4064343.6 0.0918007 0.230286 0.243625 0.222832 0.4111423.1 0.0914084 0.231071 0.244017 0.223617 0.4107492.0 0.0910161 0.229894 0.243233 0.222832 0.4095721.2 0.0914084 0.231463 0.244410 0.223225 0.4123190.2 0.0965084 0.231856 0.244802 0.227148 0.41192613.1 0.0937623 0.222832 0.236171 0.225186 0.39858817.1 0.0933699 0.220479 0.234209 0.226756 0.393880
C 1350 1394.99 1606.04 1669.68 1676.046.0 0.458219 0.486858 0.98117 0.819145 0.8191455.4 0.458219 0.484896 0.99765 0.816399 0.8116914.7 0.458611 0.483719 0.98588 0.810514 0.8061993.6 0.462142 0.484504 0.97842 0.823068 0.8222833.1 0.462927 0.485681 0.98627 0.815222 0.8101222.0 0.461750 0.483327 0.98431 0.808160 0.8081601.2 0.463711 0.484896 0.97803 0.815222 0.8112990.2 0.463319 0.488819 0.98588 0.804629 0.80109813.1 0.451157 0.485681 0.97058 0.830522 0.82659917.1 0.447234 0.486465 0.97372 0.836014 0.832091
57