simultaneous interrogation of refractive index at various
TRANSCRIPT
399 | P a g e
Simultaneous Interrogation of Refractive Index at Various
Temperatures employing a Passive Fiber Optic U-Shaped Sensor
Using a Tunable Light Source
S. Srinivasulu1 & Dr. S. Venkateswara Rao
2
1 Senior Research Fellow (SRF), Department of Physics, JNTUH – College of Engineering
Hyderabad, J N T University Hyderabad, Telangana State, India.
2 Professor of Physics, Department of Physics, JNTUH – College of Engineering Hyderabad, J N T
University Hyderabad, Telangana State, India.
ABSTRACT: Fiber optic sensors have become more popular over the conventional sensors like
mechanical sensors, chemical sensors, electrical sensors and bio-medical sensors etc, due to their
advantages with reference to sensitivity, size, weight, cost, safety and security, reliability, longevity
and flexibility in implementation and so on and so forth, for the last three and half decades since their
inception around 1970. An advanced sensor for detecting changes in chemical parameters comprises
a sensing U-shaped glass rod as core surrounded by a sensitive cladding, the absorption coefficient
which various due to the changes in chemical parameters, when applied as the cladding and a pair of
two transmissive optical fibers having a core surrounded by an insensitive cladding for connecting to
a remote light source and a detector. The changes in the output optical power with respect to the
changes in the concentration of the liquid cladding i.e. Toluene and tert-Butanol surrounding the U-
shaped glass rod used to determine the refractive index simultaneously at the operating wavelengths
of 630nm, 660nm, 820nm and 850nm, by employing a tunable light source at different temperatures.
Keywords: Different temperatures, Operating wavelengths of 630nm, 660nm, 820nm and 850nm,
Refractive index, tert-Butanol, Toluene, Transmissive optical fibers, U-shaped glass rod.
INTRODUCTION Depending upon the environmental parameters to be sensed, various detecting methods and the
corresponding designs have been employed in the traditional sensing technology to measure
mechanical parameters, chemical parameters, optical parameters, electrical parameters and bio-
medical parameters and so on and so forth. The fiber optic sensors which uses optical techniques are
proved to be superior over the conventional sensors which were introduced in early 1970’s and are
almost replacing the conventional sensors across the globe. With the advent of Lasers in 1960, the
first optical fiber was demonstrated by K. C. Kao and Hockham for communication purpose for long
distance applications. During 1970’s when the optical fiber technology for communication was
developing, it was realized that the light transmission properties of optical fibers were severely
affected by certain internal and certain external perturbations. On the observation of sensitivity of
optical fibers to these internal and external perturbations in transmitting the light, a new thought
began in the scientific community across the world. This has led to the development of the subject of
fiber optic sensors and systems [1].
Sensor can be define “a device which plays the role of converting a change in the magnitude of one
parameter into a change in the magnitude of another different parameter, which can be measured more
conveniently and more accurately [2]. Various advantages of optical fiber sensors which were
attracted intensive R & D effort across the world in the development of a new class of sensors based
400 | P a g e
on optical fibers [3]. The initial developmental work of optical fiber sensors had concentrated mainly
on military applications such as undersea applications and gyroscopes for applications in ships,
aircrafts and missiles, fiber optic hydrophones for submarine and undersea applications. According to
conservative estimates, the sale of optical fiber sensors and the growth rates will reach 35% or more
during the coming decades [4].
In the general configuration of intensity modulated fiber optic sensors the measurand is used to
modulate the intensity of light transmitted through the sensors [5]. In fact intensity modulated fiber
optic sensors are most widely studied in the field of optical fiber sensors and are simple in design and
development due to the advantages of the construction and being compatible to multimode fiber optic
technology [6-8]. Various fiber optic sensors have been developed based on the parameters to be
measured, to measure several kinds of environmental parameters like transverse, longitudinal and
angular displacements, deep sea noise levels, pressure variations, surface structure, flow of pulp
suspension, vibrations, etc, reported in the literature [9-24].
The cross-talk fiber optic sensors were developed for the analog measurement of temperature and
refractive indices of liquids [25-27]. The configuration of Y-fiber coupler tip can also be exploited to
construct an optical fiber refractometer [28]. A macro-bend based intensity modulated sensor is
reported for the measurement of temperature [29-33]. A bare tapered multimode fiber has been used
as a refractometer in another configuration [34]. Takeo et al have reported a fiber optic refractometer
in which plastic clad silica (PCS) fiber has been bent into the form of a U-shape by removing plastic
cladding from a section of fiber [35].
EXPERIMENTAL DETAILS
The construction of experimental arrangement consist of a pair of PCS fibers of 200/230μm core and
cladding diameters respectively, a tunable light source of operating wavelengths at 630nm, 660nm,
820nm and 850nm, a light detector of detectability at various wavelengths, a thermometer of dynamic
range from 0oC to 100
oC, an electrical kettle to increase the temperature of the chemical solution and
a special arrangement of ice bath to decrease the temperature of chemical solution to 10oC.
The U-shaped glass rod acting as a core in the sensing zone has the same diameter as that of the core
of the transmissive fiber and the refractive indices of sensitive and insensitive cladding are less than
the refractive indices of cores of both transmissive optical fiber and sensing U-shaped glass rod. The
experiment is carried out in three parts.
PART-I: In the first part of the experimentation two chemicals i.e. 1. Toluene and 2. tert-Butanol
have been used with a view to have various range of concentrations (20ml+0ml, 18ml+2ml,
16ml+4ml, 14ml+6ml, 12ml+8ml, 10ml+10ml, 8ml+12ml, 6ml+14ml, 4ml+16ml,2ml+18ml,
0ml+20ml) of liquids ranging from 1.493nD to 1.382nD at room temperature. Both the liquids have
been taken in different proportions making the total volume 20ml using a two burette system and
employing Automatic Digital Refractometer of modal number RX-7000i (Atago make), the refractive
index of each mixture was determined at different temperature and each liquid is preserved in an air
tight glass bottle.
PART-II: The experimental arrangement of fiber optic U-shaped passive sensor to increase the
temperature of the chemical solution is shown in figure [1].
401 | P a g e
Fig.-1: The experimental arrangement of fiber optic U-shaped passive sensor –
Setup to increase the temperature of the chemical solution.
In the second part of the experimentation the U-shaped glass rod is immersed in first mixture (20ml of
Toluene + 0ml of tert-Butanol) and the temperature of the mixture is raised to 60oC in steps of 5
oC
using an electric kettle heater and at each temperature the output power was noted at the operating
wavelength of 630nm. The experiment is repeated by employing the operating wavelengths of 660nm,
820nm and 850nm. Immersing the U-shaped glass rod into different mixtures and employing 630nm,
660nm, 820nm and 850nm source wavelengths, the experiment is repeated by noting down the output
power values at different temperatures.
PART-III: The experimental arrangement of fiber optic U-shaped passive sensor to reduce the
temperature of the chemical solution is shown in figure [2].
Fig.-2: The experimental arrangement of fiber optic U-shaped passive sensor –
Setup to reduce the temperature of the chemical solution.
402 | P a g e
In the third part of experimentation the U-shaped glass rod is immersed into the first mixture (20ml of
Toluene + 0ml of tert-Butanol) in the glass beaker and the glass beaker in-turn is placed in the ice bath
for reduction of the temperature. The power is launched from the source operating at the wavelength
of 630nm and power reaching the detector is noted for temperatures ranging from 10oC to 30
oC in
steps of 5oC. The experiment is repeated by employing 660nm, 820nm and 850nm of source
wavelengths. Taking other chemical mixtures one by one the experiment is repeated and the output
powers corresponding to each wavelength at different temperatures were noted down against the
concentration.
Standard chemical properties of Toluene and tert-Butanol
Toluene (C7H8) tert-Butanol (C4H10O)
Structure
Molar Mass (g/mole) 92.141 74.123
Refractive index (n) 1.4967 at 20oC 1.3847 at 20
oC
Density (kg/m3) 0.8697 10
3 at 20
oC 0.7886 10
3 at 20
oC
Color Colorless Colorless
Boiling Point (oC) 110.6
oC 82.3
oC
RESULTS AND DISCUSSION
The light transmission does not suffer any loss during its transmission in the insensitive parts i.e. in
the pair of two PCS fibers, but it does suffers a substantial loss during its transmission along the
sensitive part i.e. along the U-shaped glass rod. The loss happens in the sensing zone is due to two
factors.
1. Due to U-shaped macro bending of the glass rod.
2. Due to the concentration of the liquid mixture.
Depending upon the thickness of the U-shaped glass rod and radius of curvature of U-shaped glass
rod, a fraction of light escapes into the liquid cladding as an evanescent wave. The loss of light
increases as radius of curvature of glass rod decrease and the loss increases as thickness of the rod
decreases. More is the refractive index of the liquid greater is the loss of the output power in the
detector. All the above results have been noted and tabulated for further use in the experimentation
[Tables 1-5].
403 | P a g e
Table.1: Mole fraction and concentration of t-Butanol in Toluene + t-Butanol chemical mixture and
Refractive indices of mixtures at various temperatures.
S.
No.
Mole
fraction
of t-
Butanol
Refractive Index at various temperatures
10oC 15oC 20oC 25oC 30oC 35oC 40oC 45oC 50oC 55oC 60oC
1 0.0000 1.50915 1.50591 1.50171 1.49770 1.49325 1.48974 1.48582 1.48293 1.47795 1.47509 1.47102
2 0.0897 1.49411 1.49121 1.48884 1.48582 1.48215 1.47922 1.47588 1.47308 1.46901 1.46528 1.46211
3 0.1815 1.48305 1.48070 1.47721 1.47470 1.47102 1.46870 1.46528 1.46230 1.45905 1.45602 1.45323
4 0.2755 1.47413 1.47172 1.46821 1.46592 1.46211 1.45923 1.45602 1.45382 1.45070 1.44600 1.44282
5 0.3716 1.47413 1.45923 1.45602 1.45523 1.45008 1.44800 1.44402 1.44176 1.4387 1.43548 1.43209
6 0.4701 1.45008 1.44702 1.44441 1.44176 1.43808 1.43548 1.43221 1.42981 1.42603 1.42331 1.42002
7 0.5710 1.43915 1.43692 1.43327 1.43021 1.42712 1.42428 1.42183 1.41821 1.41600 1.41200 1.40798
8 0.6743 1.42603 1.42397 1.42082 1.41707 1.41404 1.41131 1.40821 1.40530 1.40258 1.39973 1.39602
9 0.7802 1.41529 1.41221 1.40930 1.40618 1.40311 1.40054 1.39752 1.39407 1.39112 1.38848 1.38575
10 0.8887 1.40311 1.40054 1.39770 1.39464 1.39112 1.38872 1.38516 1.38273 1.37902 1.3767 1.37376
11 1.0000 1.39407 1.39139 1.38848 1.38598 1.38205 1.37902 1.37561 1.37292 1.36971 1.3663 1.36312
Table.2: Mole fraction and concentration of t-Butanol in Toluene + t-Butanol chemical mixture and
Output power at various temperatures for the operating wavelength of the source 630nm
S.
No.
Mole
fraction of t-
Butanol
Concen-
tration
of t-
Butnaol
Output Power (dBm) at various temperatures
10oC 15oC 20oC 25oC 30oC 35oC 40oC 45oC 50oC 55oC 60oC
1 0.0000 0% -44.90 -44.53 -44.17 -43.73 -43.33 -42.97 -42.57 -42.27 -41.77 -41.47 -41.10
2 0.0897 10% -43.43 -43.13 -42.83 -42.57 -42.20 -41.80 -41.53 -41.33 -40.93 -40.53 -40.20
3 0.1815 20% -42.33 -42.03 -41.73 -41.43 -41.10 -40.87 -40.53 -40.23 -39.90 -39.57 -39.30
4 0.2755 30% -41.40 -41.13 -40.83 -40.57 -40.20 -39.93 -39.57 -39.33 -39.07 -38.57 -38.27
5 0.3716 40% -41.40 -39.93 -39.57 -39.50 -39.00 -38.80 -38.40 -38.13 -37.87 -37.53 -37.20
6 0.4701 50% -39.00 -38.70 -38.43 -38.13 -37.83 -37.53 -37.23 -36.97 -36.60 -36.33 -36.03
7 0.5710 60% -37.93 -37.73 -37.30 -37.07 -36.70 -36.40 -36.17 -35.83 -35.60 -35.20 -34.83
8 0.6743 70% -36.63 -36.37 -36.07 -35.70 -35.40 -35.13 -34.90 -34.60 -34.27 -33.97 -33.60
9 0.7802 80% -35.53 -35.23 -35.00 -34.63 -34.33 -34.00 -33.70 -33.43 -33.10 -32.83 -32.53
10 0.8887 90% -34.33 -34.00 -33.77 -33.47 -33.10 -32.87 -32.50 -32.27 -31.93 -31.67 -31.33
11 1.0000 100% -33.43 -33.13 -32.83 -32.57 -32.23 -31.93 -31.57 -31.23 -30.97 -30.60 -30.30
Table.3: Mole fraction and concentration of t-Butanol in Toluene + t-Butanol chemical mixture and
Output power at various temperatures for the operating wavelength of the source 660nm
404 | P a g e
S.
No.
Mole
fraction
of t-
Butanol
Concen-
tration of
t-Butnaol
Output Power (dBm) at various temperatures
10oC 15oC 20oC 25oC 30oC 35oC 40oC 45oC 50oC 55oC 60oC
1 0.0000 0% -45.23 -44.87 -44.47 -44.07 -43.63 -43.27 -42.87 -42.57 -42.03 -41.80 -41.40
2 0.0897 10% -43.73 -43.43 -43.17 -42.87 -42.53 -42.10 -41.87 -41.60 -41.20 -40.83 -40.50
3 0.1815 20% -42.60 -42.30 -42.00 -41.77 -41.40 -41.17 -40.83 -40.53 -40.20 -39.90 -39.63
4 0.2755 30% -41.73 -41.47 -41.13 -40.87 -40.50 -40.23 -39.90 -39.67 -39.37 -38.90 -38.57
5 0.3716 40% -41.73 -40.23 -39.90 -39.83 -39.30 -39.10 -38.70 -38.43 -38.17 -37.83 -37.50
6 0.4701 50% -39.30 -39.00 -38.73 -38.43 -38.10 -37.83 -37.53 -37.27 -36.93 -36.63 -36.30
7 0.5710 60% -38.23 -38.00 -37.63 -37.30 -37.00 -36.70 -36.47 -36.13 -35.93 -35.50 -35.13
8 0.6743 70% -36.93 -36.67 -36.37 -36.00 -35.70 -35.43 -35.23 -34.83 -34.57 -34.27 -33.90
9 0.7802 80% -35.83 -35.53 -35.30 -34.93 -34.63 -34.33 -34.03 -33.67 -33.40 -33.13 -32.87
10 0.8887 90% -34.63 -34.33 -34.07 -33.73 -33.40 -33.17 -32.80 -32.57 -32.20 -31.97 -31.67
11 1.0000 100% -33.67 -33.43 -33.13 -32.90 -32.50 -32.20 -31.87 -31.57 -31.27 -30.90 -30.60
Table.4: Mole fraction and concentration of t-Butanol in Toluene + t-Butanol chemical mixture and
Output power at various temperatures for the operating wavelength of the source 820nm
S.
No.
Mole
fraction of
t-Butanol
Concen-
tration
of t-
Butnaol
Output Power (dBm) at various temperatures
10oC 15oC 20oC 25oC 30oC 35oC 40oC 45oC 50oC 55oC 60oC
1 0.0000 0% -46.87 -46.47 -46.17 -45.73 -45.30 -44.93 -44.57 -44.27 -43.77 -43.43 -43.07
2 0.0897 10% -45.53 -45.13 -44.80 -44.57 -44.20 -43.80 -43.50 -43.30 -42.93 -42.47 -42.20
3 0.1815 20% -44.47 -44.00 -43.73 -43.40 -43.07 -42.87 -42.47 -42.23 -41.87 -41.57 -41.30
4 0.2755 30% -43.37 -43.13 -42.80 -42.57 -42.20 -41.93 -41.57 -41.33 -41.07 -40.73 -40.23
5 0.3716 40% -43.37 -41.93 -41.57 -41.50 -41.00 -40.80 -40.37 -40.13 -39.87 -39.50 -39.20
6 0.4701 50% -41.00 -40.70 -40.43 -40.13 -39.80 -39.50 -39.23 -38.97 -38.60 -38.33 -37.90
7 0.5710 60% -39.97 -39.63 -39.30 -39.00 -38.70 -38.40 -38.17 -37.80 -37.60 -37.20 -36.80
8 0.6743 70% -38.73 -38.37 -38.00 -37.70 -37.37 -37.10 -36.87 -36.50 -36.27 -35.93 -35.60
9 0.7802 80% -37.50 -37.23 -37.00 -36.57 -36.33 -36.00 -35.70 -35.37 -35.10 -34.80 -34.53
10 0.8887 90% -36.33 -36.00 -35.73 -35.40 -35.10 -34.83 -34.50 -34.27 -33.90 -33.63 -33.30
11 1.0000 100% -35.37 -35.13 -34.80 -34.57 -34.20 -33.90 -33.53 -33.20 -32.97 -32.57 -32.30
Table.5: Mole fraction and concentration of t-Butanol in Toluene + t-Butanol chemical mixture and
Output power at various temperatures for the operating wavelength of the source 850nm
S.
No.
Mole
fraction of
t-Butanol
Concen-
tration
of t-
Butnaol
Output Power (dBm) at various temperatures
10oC 15oC 20oC 25oC 30oC 35oC 40oC 45oC 50oC 55oC 60oC
1 0.0000 0% -47.20 -46.87 -46.43 -46.00 -45.63 -45.23 -44.87 -44.53 -44.03 -43.77 -43.43
2 0.0897 10% -45.73 -45.40 -45.17 -44.87 -44.50 -44.10 -43.83 -43.60 -43.17 -42.80 -42.47
3 0.1815 20% -44.60 -44.33 -44.00 -43.73 -43.43 -43.13 -42.80 -42.50 -42.20 -41.87 -41.60
4 0.2755 30% -43.70 -43.47 -43.10 -42.87 -42.47 -42.23 -41.87 -41.67 -41.27 -40.90 -40.57
5 0.3716 40% -43.70 -42.23 -41.87 -41.80 -41.30 -41.10 -40.70 -40.40 -40.13 -39.83 -39.50
405 | P a g e
6 0.4701 50% -41.30 -41.00 -40.73 -40.40 -40.10 -39.83 -39.53 -39.27 -38.93 -38.60 -38.23
7 0.5710 60% -40.20 -39.93 -39.60 -39.30 -39.00 -38.70 -38.47 -38.13 -37.90 -37.50 -37.13
8 0.6743 70% -38.90 -38.67 -38.33 -38.00 -37.70 -37.43 -37.20 -36.83 -36.53 -36.27 -35.87
9 0.7802 80% -37.83 -37.53 -37.30 -36.93 -36.63 -36.30 -36.00 -35.67 -35.40 -35.10 -34.83
10 0.8887 90% -36.63 -36.30 -36.07 -35.70 -35.40 -35.17 -34.80 -34.50 -34.23 -33.97 -33.63
11 1.0000 100% -35.67 -35.43 -35.10 -34.87 -34.47 -34.23 -33.90 -33.57 -33.30 -32.90 -32.60
The mole fraction and concentration of t-Butanol have been determined in the mixture of Toluene + t-
Butanol and graphs are plotted between refractive index verses mole fraction and concentration at
different temperatures and also the dependence of all the three parameters on one another have been
shown graphically [fig. 3-5].
Fig.3: Relation between Mole fraction of
t-Butanol in Toluene + t-Butanol solution
and Refraction index.
Fig.4: Relation between Concentration of t-
Butanol in Toluene + t-Butanol solution and
Refraction index.
406 | P a g e
Fig.5 Relation between Mole fraction of t-Butanol in Toluene + t-
Butanol solution, Refraction index and Temperature.
The variation of output power and mole fraction of t-Butanol in Toluene + t-butanol chemical mixture
at different temperature and at different operating wavelengths of source have been shown [fig. 6-9].
Fig.6: Relation between Mole fraction of t-Butanol in
Toluene + t-Butanol solution and Output power for
operating wavelength of the source 630nm.
Fig.7: Relation between Mole fraction of t-Butanol in
Toluene + t-Butanol solution and Output power for
operating wavelength of the source 660nm.
407 | P a g e
Fig.8: Relation between Mole fraction of t-Butanol in
Toluene + t-Butanol solution and Output power for
operating wavelength of the source 820nm.
Fig.9: Relation between Mole fraction of t-Butanol in
Toluene + t-Butanol solution and Output power for
operating wavelength of the source 850nm.
The behavior of output power with respect to temperature for different chemical mixtures and for
different wavelengths have been shown graphically in figure [fig. 10-13].
Fig.10: Relation between Temperature and Output
power of Toluene + t-Butanol solution for operating
wavelength of the source 630nm.
Fig.11 Relation between Temperature and Output
power of Toluene + t-Butanol solution for operating
wavelength of the source 660nm.
408 | P a g e
Fig.12: Relation between Temperature and Output
power of Toluene + t-Butanol solution for operating
wavelength of the source 820nm.
Fig.13: Relation between Temperature and Output
power for of Toluene + t-Butanol solution operating
wavelength of the source 850nm.
The depends of output power, refractive index, temperature at the wavelengths of 630nm, 660nm,
820nm and 850nm for different chemical mixtures represented by corresponding refractive indices on
one another have been shown in figures [fig. 14-17].
Fig.14: Relation between Refractive index, Output
Power and Temperature of Toluene + t-Butanol
solution for operating wavelength of the source
630nm.
Fig.15: Relation between Refractive index, Output
Power and Temperature of Toluene + t-Butanol
solution for operating wavelength of the source
660nm.
409 | P a g e
Fig.16: Relation between Refractive index, Output
Power and Temperature of Toluene + t-Butanol
solution for operating wavelength of the source
820nm.
Fig.17: Relation between Refractive index, Output
Power and Temperature of Toluene + t-Butanol
solution for operating wavelength of the source
850nm.
CONCLUSION From the above interrogation, it is concluded that as the concentration of Toluene increases in the
binary mixture of Toluene + tert-Butanol, the refractive index of the guiding liquid also increases. It is
also observed that for all the wavelengths i.e. 620nm, 660nm, 820nm & 850nm, with increasing the
refractive index of guiding medium the output power decreases and hence power loss increases. The
graphs showing the variation of output power with the variation of the refractive index and
temperature of the guiding chemical solution can be used as calibration curves to measure the
refractive index of the unknown liquids or chemicals or bio-fluids, etc in the dynamic range of
1.363nD to 1.509nD at the temperatures from 10oC to 60
oC and operated at the wavelengths of 630nm,
633nm, 660nm, 820nm and 850nm. This method is useful in chemical, pharmaceutical, food and
beverage industries, where conventional methods fail to determine the refractive index of liquids at
higher temperatures.
REFERENCES
[1] B. Culshaw, “Fiber optic sensing and signal processing”, Peter Pereginus, Stevenage (1984).
[2] J. P. Dakin, “Optical fiber sensors”, Summer school on “Principles of optical systems” held at
Rose Priori, organized by Strathclyde University, Glasgow, May (1987).
[3] T. G. Giallorenzi, Bucaro J. A., Dandridge A., Cole J. H., Rashlwy S. C. and Priest R. G., “Optical
fiber sensor technology”, J. Quant, Electron., Vol. QE-18, pp. 626-665, (1982).
[4] “The outlook for optical fiber sensors”, published by decision resources, Arthur D. Little,
Burlington, MA, (1989).
[5] C.M. Davis, Carome E.E., Weil M.H., Ezekiel S. and Einzig R.E., “ Fibre Optic Senors
Technology Handbook”, Dynamic Systems Inc., Virginia (1982).
[6] G.D. Pitt, Extance P., Neat R.C., Batchelder D.N., Jones R.E., Barnett J.A. and Pratt R.H.,
“Optical Fibre Sensors”, Proc. IEE 132, pt. J., 214-218 (1985).
410 | P a g e
[7] R.S. Medlock, “Fibre Optic Intensity Modulated Sensors” in “Optical Fibre Sensors”, Ed. By A.N.
Chester, S. Martelluci and A.M. Verga Scheggi, Martinus Nijhoff, Dordrecht (1987).
[8] D.A. Krohn, “Fibre Optic Sensors-Fundamentals and Applications”, Instrument Society of
America (1988).
[9] R.N. Chakraborty and Pal B.P., Internal Study on “Development of a Fibre Optic Fusion Splicing
Machine”, IIT Delhi (1985).
[10] W.B. Spillman and Gravel R.L., “Moving Fibre Optic Hydrophone”, Opt. Letts. 5, 30-33 (1980).
[11] W.B. Spillman and McMohan D.H., “Schlieren Multimode Fibre Optic Hydrophone”, App.
Phys. Letts. 37, 145-147 (1980).
[12] M. Priyamvade and Pal B.P., Internal Study on “Fabrication of Fused Y-Coupler”, IIT Delhi
(1989).
[13] N.R. Paramanthan and Pal B.P., Internal Study on “Fibre Optic Acoustic Sensors”, IIT Delhi
(1984).
[14] W.B. Spillman and McMohan D.H., “Frustrated Total Internal Reflection Multimode Fibre Optic
Hydrophone”, App. Opt. 19, 113-117 (1980).
[15] L.H. Limdstrpem, “Miniatusied Pressure Transducer Intended for Intravascular Use”, IEEE
Trans. On Bio-medic. Engg. BME-17, 207-219 (1970).
[16] C.R. Tallman, Wingate F.P. and Ballard E.O., “Fibre Optic Coupled Pressure Transducer”, ISA
Trans. 19, 49-51 (1980).
[17] H. Matsmoto, Saegusa M., Saito K. and Mizoi K., “The Development of a Fibre-Optic Catheter-
tip Pressure Transducer”, J.Med. Engg. Tech. 2, 239-242 (1978).
[18] S. Uena, “New Method of Detecting Surface Texture by Fibre Optics”, Bull. Japan Soc. Of Prec.
Engg. 7, 87-90 (1973).
[19] K. Oki, Akehata T. and Shiarai T., “A New Method of Evaluating the Size of Moving Particles
with a Fibre Optic Probe”, Powder Tech. 11, 51-54 (1975).
[20] M.A. Nokes, Hill B.C. and Barelli A.E., “Fibre Optic Heterodyne Interferometer for Vibration
Measurements in Biological Systems”, Rev. Sc. Instrum. 49, 722-728 (1978).
[21] K. Kyuma, Tai S., Hamanaka K. and Nuhoshita M., “Laser Doppler Velocimeter with a Novel
Fibre Optic Probe”, App. Opt. 20, 2424-2428 (1981).
[22] A.L. Harmer, “Optic Fibre Sensors”, A Survey Report prepared by Battele-Geneva Research
Centre, Switzerland.
[23] F.Parmigiani, “A High Sensitivity Laser Vibration Meter Using a Fibre-Optic Probe”, Opt.
Quant. Electron. 10, 533-537 (1978).
411 | P a g e
[24] S. Uena, Shibata N. and Tsujiuchi J., “Flexible Coherent Optical Probe for Vibration
Measurements”, Ppt. Commn. 23, 407-410 (1977).
[25] S.Ramakrishna and R. Th. Kersten, “A multipurpose cross-talk sensor using multimode fibres”,
Proc. 2nd
Opt. Fibre Sensor Conf., Stuttgart, 105-110 (1984).
[26] S.Ramakrishna, “Multimode Optical Fibre Sensors”, J.I.E.T.E. (India) 32, 307-310 (1986).
[27] S.Ramakrishna and R. Th. Kersten, “Faseroptic Sensor mit Uberwachugsmoglichkeiten”,
German Patent P. 3415242 (1984).
[28] S.Ramakrishna and R. Th. Kersten, “Faseroptische Flussigkeitsbrechzahl-Messvorichtung”,
German Patent P. 3303089 (1983).
[29] N. Lagakos, Litovitz T., Macedo P., Mohr R. and Meister R., “Fibre Optic Displacement Sensor”
Advances in Cermics 2, Ed. B. Bendow and S.S. Mitra, Am. Ceram. Soc. Bull 539-545 (1981).
[30] J.N. Fields, Asawa C.K., Smith C.P and Morrison R.J., “Fibre Optic Hydrophone’, Advances in
Ceramics 2, Ed. B. Bendow and S.S. Mitra, Am. Ceram. Soc., 529-539 (1981).
[31] W.H.G.Horsthuis and Fluitman J.H.J., “The Development of Fibre Optic Microbend Sensors”,
Sensors and Actuators 3, 99-110 (1982/83).
[32] J.N. Fields and Cole J.H., “Fibre Microbend Acoustic Sensor”, App. Opt. 19, 3265-3267 (1980).
[33] N. Lagakos, Litovitz T., Macedo P., Mohr R. and Meister R., “Multimode Optical Fibre
Displacement Sensor”, App. Opt. 20, 167-170 (1981).
[34] A. Kumar, Subrahmoniam T.V.B., Sharma A.D., Thyagarajan K., Pal B.P. and Goyal I.C., “A
Novel Refractometer using Tapered Optical Fibres”, Electron. Letts. 20, 534-535 (1984).
[35] A. Ankiewicz, Pask C. and Snyder A., “Slowly Varying Tapers”, J. Opt. Soc. Am. 72, 198-2-3
(1982).
AUTHORS:
S. SRINIVASULU [M.Sc.(Physics), M.Sc.(Maths), B.Ed., BLISc., CSIR-UGC
NET, LMISCA] UGC–Senior Research Fellow (SRF), Department of Physics,
JNTUH-College of Engineering Hyderabad, Jawaharlal Nehru Technological
University Hyderabad, Telangana State, India. He has published 24 research
papers in reputed International Journals including UGC Recognized Journals and
UGC-CARE approved Scopus and Web of Science Journals. He has received
IARDO-Young Scientist Award for the year 2018, Researcher of the Year–2019,
Active Young Researcher Award and Outstanding Research Scholar Award.
412 | P a g e
Dr. S. VENKATESWARA RAO [M.Sc. (Solid State Physics), Ph.D. (Fiber
Optic Sensors), MISTE, MISCA] Professor and Chairman Board of Studies in
Physics at Jawaharlal Nehru Technological University Hyderabad, Kukatpally,
Hyderabad, Telangana State, India. He has 30 Years of teaching and research
experience in Physics. He has published many research papers in National and
International reputed Journals including UGC Recognized Journals and UGC-
CARE approved Scopus and Web of Science Journals. Prof. S. V. Rao
Received more than 10 International Awards for his Teaching and Research.