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1. Introduction
The increasing demand for electrical power, and the rapid depletion and environmental concerns of fossil fuels have prompted the increased need for alternate forms of clean and sustainable energy sources. Globally there is an unassertive move away from unabated coal, and the rise of renewable energies from under 30% of generation in 2020 to above 40% in 2030 [1]. According to statistics (2021) put out by International Renewable Energy Agency (IRENA), an entire of 2,802,004 MW of electricity generation was produced worldwide in 2020, added by 53,824 MW of electricity generation from Africa [2]. The International Energy Agency (IEA) projected that the worldwide energy mandate would be twofold by 2030 [3]. The global energy generation, ingesting, and financial development (1991–2017) swing displays a direct upsurge associated with the growing development of the global economy [4]. These cited worldwide trends of financial development mutually with industrial development and countryside electrification energy requirements are reflected in South Africa. South Africa’s energy source is a mixture of 59% from carbon coal, 16% from petroleum, 3% from gasoline, 2% nuclear, and 20% from renewable resources and leftover [4, 5]. The worldwide cumulative swing of wind energy facility systems has speedily extended the wind energy facilities [6]. The wind is the gross effect of the pressure rise force, gravity, Coriolis, centrifugal and friction forces performing on the troposphere. The wind’s aerodynamic features, lift and drag, angle of attack, and the effect of a high lift to drag ratio as the highest draft feature of the turbine rotor blade for effective wind power harvesting as explained in [7].
In [8], it was discussed how the twisted and tapered propeller-type rotor blades, could improve the angle of attack, rotor speed, and efficiency while reducing drag and bending stress. Betz equation evaluation of the wind energy conversion signifies that 59% optimum efficiency in which a conventional wind turbine can extract power from the wind [9]. Wind turbines generator systems are generally classified in lift and drag type, upwind and downwind type, and horizontal and vertical axis turbines. Most power utility networks operate either as N + 1 or N + 2 configuration criteria. N-0 configuration criterion is widely practiced in radial low voltage distribution networks [10]. A grid-connected wind energy system needs to meet certain standards before being integrated into the grid. Wind turbine generators control system (WTGCS) connects wind turbine generators to the grid, with a generation scheduling in place, that regulates the generator speed consequently adjusting the generator frequency, the voltage at the grid, active and reactive power flow using rotor side converter (RSC) and the grid side converter (GSC) and at the same time prefer to disconnect the wind turbines from the grid during faults, resulting in power losses, out of synchronization, and cascaded tripping of generation facilities [11].
The study in [12], clarifies in what way the controlled rotor current on the rotor side converter and a dynamic disruption elimination control by the resources of an extended state observer (ESO) controller the real and reactive stator powers produced by a wind power transformation method. In [13], an MPPT is combined with the DFIG stator flux oriented vector control to disassociate the control of real and reactive power produced by the DFIG centered wind turbine, with the generated power plattering as the dynamic energy reference for the DFIG. In [14], unit 3 directs the symmetrical and asymmetrical voltage rise and fall of the power grid-integrated DFIG, by including further current controller loops by disintegrating the vectorial references into progressive and undesirable signal indications. In [15], an open circuit stator negative sequence rotor current control system is applied, permitting the induced stator voltage to develop as unbalanced as the grid system voltage, henceforth allowing an even linking of DFIG to the power grid system. In [16], a wind speed assessment process centered on particle swarm optimization, and support vector regression, was evaluated to allow the MPPT control. The South African Renewable Energy Grid Code (SAREGC) published narration (2.9) in November 2016 stipulates the necessities for manufacturing standards, networking reliability, and unbalanced admittance to the power grid using RPPs.
This chapter aims to investigate the impact of wind energy penetration into the distribution grid for different percentages for the different scenarios of wind energy integration into the existing grid.
2. Aerodynamics, electrical, and drive train modeling
2.1 Aerodynamics modeling
The wind is the net result of the pressure gradient force, gravity, Coriolis, centrifugal and friction forces acting on the atmosphere. Since wind speed usually varies from one location to another and also fluctuates over time in a stochastic way, J.G. Slootweg [17] proposed a mathematical model that takes some landscape parameters to generate a wind speed Vmt in (meter/sec) sequence for any location, as per equation one:
Vwt=Vwat+Vwrt+Vwgt+VwttE1
Where, Vwat is a constant component, Vwrt is a common ramp component, Vwgt is a gust component, and Vwtt is a turbulence component in (meter/sec).
The operation of a wind turbine can be characterized by its mechanical power output Pm through a cross-sectional area A normal to the wind as a function of wind speed Vw [18].
Pm=0.5ρAVw3CPαβE2
Where ρ is the air mass density, A=πr2 is the turbine swept area, r is the turbine radius, and Vw is the wind speed. Cp is a nonlinear function of λ and β is referred to as the performance coefficient and is smaller than 0.59, given by [18, 20].
Cp=0.5rCfλ−0.022β−2e−0.255rCfλE3
Where β is the turbine pitch angle, λ is the tip-speed ratio, and Cf is the blade design constant λ is defined by:
λ=rωturVwE4
Where ωtur is the rotational angular speed of turbine blades in mechanical rad/sec.
Pmmax=0.5ρAr3CPmaxλopt3wtur3=Koptwtur3E5
Eq. (5) indicates that Pmax is proportional to the cube of turbine speed, hence the mechanical torque Tmmax is:
Tmmax=Koptwtur2E6
2.2 Electrical modeling
A wounded-rotor induction motor can operate as a double-fed induction motor (DFIM) with the stator side windings openly attached to the three-phase power grid/load and the rotor side windings attached to a side-by-side moderately measured (20–30) % rating power converter as shown in Figure 1. As shown in Figure 2, an induction motor works on the interface principle between the stator and rotor magnetomotive forces (MMF). The stator side windings current produce an MMF revolving at power grid side frequency especially including an MMF in the rotor side windings. The rotor speed does not compliment the stator side MMF. This induced rotor MMF will rotate at the so-called slip frequency which possesses the subsequent value [21]:
Figure 1.
Grid-connected DFIG [19].
Figure 2.
Electrical modeling of an induction machine winding layout [21].
ωslip=ωmmfrotor=ωmmfstator−ωrotorE7
Where, ωslip is the slip frequency, corresponding to the frequency of rotor current and voltage, ωmmfstator is the stator or the grid frequency in (rad/sec), ωrotor is the rotor rotating frequency (rad/sec). In both sub-synchronous and super-synchronous operations, the DFIM machine can be operated either as a motor (0 < slip<1) with positive rotor torque or a generator (slip<0) with negative rotor torque. The Park and Clark transform allowing the transformation of time-dependent variables into constant values. The per-unit electromagnetic torque equation expressed in d-q park reference is given by [22]:
Te=φdsIqs−φqsIds=φqrIdr−φdrIqr=LmIqsIdr−IdsIqrE8
Neglecting the power losses associated with the stator and rotor resistances, the active and reactive stator powers for the DFIG are [22]:
Ps=32VdsIds+VqsIqsE9
Qs=32VqsIds−VdsIqsE10
And the active and reactive rotor powers are given by:
Pr=32VdrIdr+VqrIqrE11
Qr=32VqrIdr−VdrIqrE12
The overall system equations can also be re-written with relation to the rotating frames [21]:
PT=Ps+Pr=32Vqr\'Iqr\'+Vdr\'Idr\'+VdsIds+VqsIqsE13
QT=Qs+Qr=32Vqr\'Iqr\'−Vdr\'Idr\'+VdsIds−VqsIqsE14
The torque expression and the stator reactive power, which are the control objectives of the rotor-side converter control, are shown in Eqs. 17 and 18. Where, p is the number of pole pairs of the generator, Iqs and Iqr are the q component of the stator and rotor current, Ids and Idr are the d component of the stator and rotor current, Vqs and Vds are the q and d components of the stator voltage. The stator and rotor flux linkages in the synchronous reference frame are expressed as [23]:
ψs=LsIs+LmIrE15
ψr=LmIs+LrIrE16
The electromagnetic torque can be expressed using the d−q components as following [23].
Tm=32pLmLsψqsIdr−ψdsIqrE17
Qs=32VqsIds−VdsIqsE18
2.3 Drive train model
Considering the mechanical aspect of the wind turbine, the mechanical representation of the drive train of the entire wind turbine is complex. Following four types of the drive train in wind turbine models are generally used [24].
Six mass drive train model.
Three mass drive train model.
Two mass drive train model.
one-mass drive train model.
Of the above four types of drive train models, the one that was modeled and implemented is the simplified form of the two mass-shaft model power train systems as shown in Figure 3 consisting of a shaft and gearbox. As per the two-mass model of the drive train system described in [24], all masses are grouped into low and high-speed shafts. The inertia of the low-speed shaft comes mainly from the rotating blades and the inertia of the high-speed shaft. The input to the model for a two-mass system is established as torque TA, which is gained by the aerodynamics methodology and the generator response torque Te. The target is the deviations in the rotor speed ωr and the generator speed ωg. The deviations in the mechanically compelled torque Tm, the generator torque response Te, and torque loss owing to friction Tfric, causes the variation of angular velocity ωg∙ [24].
Figure 3.
Schematic drawing of the two mass shaft drive train model [24].
Tm−Te−Tfric=jg×ωg˙E19
The change in the angular speed ωr· is caused by the difference between the aerodynamic torque TA and shaft torque Ts at a low speed shaft [24].
TA−Ts=jr×ωr˙E20
ω˙g=φg″andω˙r=φr″E21
Tm and Ts are connected by the gear ration, as Ts=nTm
Ts=Ks⋅Δφ+Dsφ⋅=Ks.Δφ+Dsωr−ωg/nE22
Where Ks is the stiffness constant and Ds is the damping constant of the shaft. Considering a two-mass free-swinging system the Eigen frequency is as follows:
ω˙r=1JrTA−DS⋅ωr+DSnω˙g−KS∫ωr−ωgndtE23
ω˙g=1Jg−Te−Dg+DSn2ωg+DSnω˙r−Ksn∫ωr−ωgndtE24
Where, Ks is the stiffness constant and Ds is the damping constant of the shaft. Considering a two-mass free-swinging system, the Eigen frequency is given as:
ωos=2πfos=KsJges⋅E25
The total inertia of the free-swinging system on the low-speed is calculated by:
Jges=Jr⋅Jg⋅n2Jr+Jg⋅n2E26
So, the stiffness constant Ks and the damping constant Ds of the low-speed shaft, with ξs as logarithmic decrement is:
Ks=Jges⋅2πfos2E27
Ds=2ξs⋅KsJgesξs2+4π2E28
3. Control system
3.1 Conventional wind power control scheme
Owing to the alterations in the timing measures of the mechanical and electrical gestures, the DFIM-centered wind power control system has a multiple-layer control arrangement, with unified sub-systems. At the uppermost developed control stage, a maximum power point tracking procedure is applied to compute the generator speed set-point Ωm∗ to produce the DFIG target power set point Tem∗. The other control stage oversees the turbine pitch control scheme. The third and final control stage standardizes the generator torque, the real and reactive power, and the DC linkage voltage. The key limitations of the traditional control approach are explained in [25]. In the fractional load control process, the PI controller does not permit calibration of the commutation between the energy intensification and the momentary load depreciation, and at the full load control stage, the pitch-controlled generator speed directive can source acute power variations. Therefore, this study emphasizes the generator controller utilizing an adaptable tracing, self-adjustable PI controller framework. The suggested control system is disintegrated into various sub-categories entailing the fréchet derivative, the proportional, integral, and the derivative control. The PID control variables, Kp, Ki, and Kd are observed as the adaptable interfaces among the above sub-categories to self-adjusting these variables.
A reference current calculation and current control loop are presented as shown in Figure 4 [26] and both the reference reactive power Qsref and Qgref are usually set to zero and can be modified depending on the grid requirements. The DC link reference voltage has a fixed value while the reference torque is determined by the maximum power point tracking control system. The vectorial control system of a grid-integrated DFIM is very similar to the traditional vectorial control system of a squirrel cage machine. DFIM is controlled in a synchronously revolving dq orientation structure, with the d axis adapted to the rotor flux space vector locus. The direct current is therefore related to the rotor side magnetic flux linkage although the quadrature current is related to the electromagnetic torque. By regulating autonomously, the two current modules, a disintegrated control between the torque and the rotor excitation current is achieved. Likewise, in the vectorial control system of a DFIM, the d and q axis components of the rotor current are controlled.
Figure 4.
Reference values entered in DFIG back to back converter [26].
3.2 Maximum power point control
The most commonly used wind turbine control strategy is illustrated in Figure 5, and consists of four operation zones, this shows the wind speed as a function of the wind speed [27]. This resembles an operation at full load condition. Here, the mechanical power can be restricted moreover by changing the pitch or using torque control. Usually, the electromagnetic torque is retained at an insignificant value and regulates the pitch angle to retain the wind turbine at extreme speed to maintain power output at a higher than rated wind speed.
Figure 5.
The operation zones for power point tracking for wind turbine [27].
The maximum power deviation with the rotational speed of DFIM is pre-established for every individual wind turbine. Owing to the intermittent character of the wind, it is vital to comprise a control unit to be able to follow maximum peak irrespective of the wind speediness. Due to the adaptive tracking and self-tuning capabilities, the two best MPC control methods are described in [27] as indirect speed control and direct speed control. The direct speed controller (DSC) as shown in Figure 6 follow the maximum power curve more narrowly with rapid dynamics. Observing the description of the tip speed ratio, the optimum VSWT rotating speed Ωtopt may be established from the wind speed Vw, whereas Tem is the turbine electromagnetic torque, Ωm is rotating speed, Tt_est is assessed turbine aerodynamics torque, and Pmax is the maximum powering point.
Figure 6.
Direct speed control [27].
Ωm∗=NTt_estkopt_tE29
Pmax=12ρπR5Cp_maxλopt3Ωm∗3E30
PMPPT=KoptΩ∗m3E31
3.3 Rotor side control
The DFIG rotor variable’s orientation must follow the orientation of the selected orientation parameter. Here, two algorithms are implemented, stator side voltage aligned control and stator side flux aligned control. Once this parameter vector is computed in the rotor side orientation structure, its comparative angle δ to the rotor side orientation structure is designed and the rotor parameters are altered into the novel control-reference structure, as shown in Figure 7 [21].
Figure 7.
Reference frames used in park transform [21].
Vector control is applied to the rotor side converter to control the stator’s active and reactive power. The direct axis loop is used to control reactive power whereas the quadrature axis is for active power control. The rotor converter obtains evaluations of rotor circuit parameters and is accountable for handling the reactive power flow between the stator and the power grid as well as regulating the generator torque. Its input parameters are not associated with the stator orientation structure. Though, it is exactly the stator target that must be measured and controlled. For the RSC to calculate an output stable with the stator’s parameters, the rotor parameters articulated in the rotor d-q orientation structure must be revolved to be oriented with the control orientation structure. The RSC controller MATLAB block diagram is shown in Figure 8.
Figure 8.
RSC controller MATLAB block diagram.
The equations used in the orientation process are [21]:
Srd=Srq\'sinδ+Srd\'cosδE32
Srq=Srq\'cosδ−Srd\'sinδE33
Where:
S\' represents a d-q rotor variable expressed in the rotor reference frame rotating at slip frequency.
S represents the same rotor variable oriented along with the control reference frame.
δ represents the alignment angle by which the rotor reference frame must be rotated.
3.4 Grid side control
The main objective of the grid side converter control model with ideal bidirectional switches as shown in Figure 9 is to focus on the active and reactive powers delivered to the grid, keeping a constant DC-link voltage independent of the value and direction of the rotor power flow, and grid synchronization control. The grid side of the wind turbine system is composed of the grid side converter, the grid side filter, and the grid voltage. It converts voltage and currents from DC to AC, while the exchange of power can be in both directions from AC to DC (rectifier mode) and from DC to AC (inverter mode). The d−q axis voltage Vgd and Vgq of the grid side converter from the original three phases Vga, Vgb, Vgc is as below [27]:
Figure 9.
Simplified converter, filter, and grid model [27].
Vgd=Vgd+RgIgd+LgdIgddt−ωsLgIgqE34
Vgq=Vgq+RgIgq+LgdIgqdt+ωsLgIgdE35
4. Simulation and discussion
4.1 Steady-state simulation
The system under study is shown in Figure 10. The 2 MW, 1500 rpm, 50 Hz, 690 V, 1760 A, and 12,732 Nm torque DFIG model was used to model and simulate the systems. The simulation was used to analyze the challenges with power system stability of integrating the WTG into the grid, considering intermittent wind characteristics and the problem of slip convergence. This task was executed by creating a steady-state Matlab function, to calculate the steady-state operation points and reveals how the rotor speed of the modeled DFIG involves the power flow of the studied system. Speed array and torque array were considered as inputs into the stimulated three-blade wind turbine connected with DFIG. Two different work frames of generation strategies Qs=0 and Idr=0 were considered here.
Figure 10.
Steady-state simulation program block model.
4.1.1 Steady-state simulation results and analysis
Simulations were carried out for variable wind speeds ranging from 5 m/s (cut-in speed) to 25 m/s (cut-off speed) in progressive steps of 2 m/s, with reactive power Qs=0, (red plot) and Idr=0 (green plot) as a control strategy separately. The results for the DFIG voltage, torque, generated real power, efficiency, and consumed reactive power in both the methods are plotted in Figures 11–18. The influence of two different generation strategies does not make big differences for variables such as Tem, Pt, Ps and Pr, however, some other variables such as Is, Ir, Qs, and Qr, (Figures 14–17) was found to have some big differences in amplitudes, concerning rotor speed.
Figure 11.
The graph of torque (Tem) vs. rotor speed (n).
Figure 12.
DFIG’s active power Pt (W) vs. speed n (rpm).
Figure 13.
DFIG stator and rotor active power Ps & Pr (W) vs. speed n (rpm).
Figure 14.
DFIG Is (A) vs. n (rpm), red plot: Qs = 0, green plot: Idr = 0.
Figure 15.
DFIG Ir (A) vs. n (rpm), red plot: Qs = 0, green plot: Idr = 0.
Figure 16.
DFIG Qs (VAR) vs. n (rpm), red plot: Qs = 0, green plot: Idr = 0.
Figure 17.
DFIG Qr (VAR) vs. n (rpm), red plot: Qs = 0, green plot: Idr = 0.
Figure 18.
DFIG Vr & vs vs. speed n (rpm), red plot: Qs = 0, green plot: Idr = 0.
Figure 11 shows the DFIG’s torque vs. speed characteristics, which stimulate the three-blade wind turbine with a minimum speed of 900 rpm and a maximum speed of 1800 rpm. The DFIG can perform above and under the synchronization speed for power generation. The generation model of DFIG matching negative torque values covers from the negative slip to the positive slip state. Therefore, the turbine target power and electromagnetic torque features of variable speed DFIGs are unlike the customized constant-speed induction machine. Figure 12 shows the plotting for the total mechanical power of the turbine shaft, which is the product of torque and speed, from sub synchronous to super synchronous speed, with a maximum power value of −2.54 MW at 1800 rpm. Figure 12 shows, the rotor’s active power Pr is absorbed by the induction machine at below synchronous speed, and the active power is supplied above the synchronous speed from the induction generator to the grid. Figure 13, shows, with Qs=0 (red plot) as an adopted control strategy the stator current value Is is on the lower side. Figures 14 and 15 shows during Idr=0 (green plot) as a control strategy the rotor current Ir is on the lower side and Qs is on the higher side. Figure 16 shows the rotor reactive power Qr=0 at synchronous speed 1500 rpm, with both control strategy Qs=0 and Idr=0, indicating the reactive power varies according to the wind turbine speed. Figure 17 shows, a constant stator voltage Vs amplitude throughout the variable speed range, while the variable rotor voltage Vr amplitude is very low at synchronous speed 1500 rpm, with two peak voltage amplitudes at a minimum and maximum rotor speeds.
4.1.2 Evaluation of simulation modeling at defined speeds
Table 1 shows the specified wind turbine DFIG speeds that are compared and used to evaluate the simulation model parameters with the steady-state model parameters as obtained from Figures 11–18. The simulation graphs shown in Figures 19 and 20 represent the torque vs. time and rotor current vs. time characteristics at 1356 rotor rpm and steady-state simulation period of 1.5 sec and 1691 rotor rpm at a steady-state simulation period of 2.0 sec for the entire modeling period of 3.0 sec. Simulated torque values −6050 Nm and − 9450 Nm, rotor current values 1200 amps and 1790 amps, and stator current values 1325 amps and 1850 amps at pre-defined speeds are close to steady-state parameter values as shown in Figures 11–18.
Sn
Speed
Torque (N-m)
Ir
Is
Vr
Steady-state
Simulation Model
Steady-state
Simulation Model
Steady-state
Simulation Model
Steady-state
Simulation Model
Steady State
Simulation Model
1
1182
1182
−4550
−4550
875
920
1090
1100
110
100
2
1356
1356
−6050
−6000
1160
1200
1325
1350
60
60
3
1691
1691
−9450
−9455
1770
1790
1850
1860
73
75
Table 1
WT simulated parameters at defined DFIG speeds.
Figure 19.
Torque vs. time graph @ 1356 rotor rpm and @ 1691 rotor rpm.
Figure 20.
Ir vs. time graph @ 1356 rotor rpm and @ 1691 rotor rpm.
4.1.3 Simulation model of DFIG using wind turbine MPPT block
In this section, a 2 MW stator power DFIG model and a three-blade wind turbine model with gear ratio n=100, blade radius 42 m, Cp=0.42, and λopt=7.2 were used for the wind turbine maximum power point tracking simulation control as shown in Figure 21. Figures 22 and 23 show the wind turbine MPPT simulation model characteristics at 8 m/sec and 10 m/sec of wind speed. Observed in Figure 11, the torque response for the wind speed and iq current indicates that more oscillations occur at the low torque due to the fact reduced mechanical inertia. The more the mechanical inertia, the more the torque oscillations. On achieving the steady-state condition at 2 sec of modeling time, wind turbine speed and correspondence torque values were tabled for angular speed of 140 rad/sec, at a torque of −5500 Nm, and a mechanical wind turbine power output approximately equal to 770 kW was obtained. Further, the wind speed was increased from 8 m/sec to 10 m/sec and the steady-state simulation at 6 sec of modeling time was observed. On achieving the steady-state at 6 sec of modeling time, wind turbine speed and correspondence torque values were tabulated for 170 rad/sec, at −8800 Nm respectively and a mathematical wind turbine power outcome equivalent to 1.49 MW was recorded. These two simulated outcomes are very close to the steady-state characteristics graph numerical values as shown in Figure 11 and Figure 12.
Figure 21.
WT MPPT control model.
Figure 22.
The dynamic state WT MPPT graph of speed vs. time (sec).
Figure 23.
WT MPPT torque vs. time characteristic curve.
5. Conclusions
This study was to focus on investigating the influences of the integration of wind power generators into the power grid systems. The rotor side converter control unit is utilized for, real and reactive power control by regulating the rotor current and the speed of the DFIG. With the computed stator voltage, stator current, rotor current, and the rotor location by encoder response signal the active PI measured and controlled procedure results in a considerable enhancement in control system sturdiness and advances its indemnity to produced system noise. The engaged PI control unit attests to the grid side converter control by sustaining the stable generated power frequency and voltage with the grid frequency and voltage. The controller scheme and the simulation mode controller employed for the study assure the wind generator supplying into the grid at varying wind speeds behaves like a synchronous generator, at a zero Hz rotor frequency.
Acknowledgments
I wish to thank the almighty God for giving me life and enabling me to reach the heights that I have reached.
I wish to thank my parents and my siblings, for their tireless and relentless love, continuous support, and the countless sacrifices they have made on my behalf. To my family, for being great inspirations and believing in us even when we have stopped believing in ourselves. This would not have been possible without the family’s help.
Finally, I wish to everyone not mentioned above but directly or indirectly contributed to our work, your input is much acknowledged.
Abbreviations
DFIGs
Double Fed Induction Generators
DSC
Direct Speed Control
ESO
Extended State Observer
GSC
Grid Side Converter
IEA
International Energy Agency
IRENA
International Renewable Energy Agency
MMF
Magnetomotive Force
MPPT
Maximum Power Point Tracking
PCC
Point of Common Coupling
RSC
Rotor Side Converter
SARGEC
The South African Renewable Energy Grid Code
VSCF
Variable Sped Constant Frequency
WECS
wind energy control System
WT
Wind Turbines
WTGCS
Wind turbine generators control system
Cf
Turbine blade density constant
Cp
E
Ks
Ds
Ps
Pr
Qs
Qr
R
Te
Per-unit electromagnetic torque in d-q park reference newton/meter
Tf
Turbine friction torque in newton/meter
Tmmax
Turbine maximum torque in Newton/meter
Vm(t)
Wind Speed in meter/sec
Vw(t)
Wind Speed of air mass of m Kg in meter/sec
Vwt(t)
Wind Speed turbulence component speed in meter/sec
Vwa(t)
Wind Speed constant component speed in meter/sec
Vgt(t)
Wind Speed gust component in meter/sec
ρ
Air density in Kg/m3
β
Turbine blade pitch angle
λ
Turbine blade tip speed ratio
ωtur
Turbine rotational angular speed in mechanical radian/sec
ωslip
Slip frequency
ωmmfstator
Slip frequency corresponding to the frequency of rotor current and voltage in radian/sec
ωrotor
Rotor rotating frequency in radian/sec
ωr
Rotor speed in radian/sec
ωg
Generator speed in radian/sec
Ψs
Ψr
\n',keywords:"renewable energy sources, DFIG’s, MATLAB/SIMULINK, WT, MPPT, distribution network, wind energy",chapterPDFUrl:"https://cdn.intechopen.com/pdfs/81489.pdf",chapterXML:"https://mts.intechopen.com/source/xml/81489.xml",downloadPdfUrl:"/chapter/pdf-download/81489",previewPdfUrl:"/chapter/pdf-preview/81489",totalDownloads:3,totalViews:0,totalCrossrefCites:0,dateSubmitted:"January 23rd 2022",dateReviewed:"February 15th 2022",datePrePublished:"April 23rd 2022",datePublished:null,dateFinished:"April 23rd 2022",readingETA:"0",abstract:"Recently, scientists and academics are discovering progressive improvements in the arena of wind power technology economically and reliably, allowing them to produce electricity focusing on renewable energy resources. Wind turbines (WT) using the Doubly Fed Induction Generators (DFIGs) have attracted particular attention because of their advantages such as variable speed constant frequency (VSCF) operation, independent control capabilities for maximum power point tracking (MPPT), active and reactive power controls, and voltage control strategy at the point of common coupling (PCC). When such resources have to be integrated into the existing power system, the operation becomes more challenging, particularly in terms of stability, security, and reliability. A DFIG system with its control strategies is simulated on MATLAB software. This entails the rapid control prototype testing of grid-connected, variable speed DFIG wind turbines to investigate the WT’s steady-state and dynamic behavior under normal and disturbed wind conditions. To augment the transient stability of DFIG, the simulation results for the active and reactive power of conventional controllers are compared with the adaptive tracking, self-tuned feed-forward PI controller model for optimum performance. Conclusive outcomes manifest the superior robustness of the feed-forward PI controller in terms of rising time, settling time, and overshoot value.",reviewType:"peer-reviewed",bibtexUrl:"/chapter/bibtex/81489",risUrl:"/chapter/ris/81489",signatures:"Ramesh Kumar Behara and Kavita Behara",book:{id:"11176",type:"book",title:"Wind Turbines - Advances and Challenges in Design, Manufacture and Operation",subtitle:null,fullTitle:"Wind Turbines - Advances and Challenges in Design, Manufacture and Operation",slug:null,publishedDate:null,bookSignature:"Prof. Karam Youssef Maalawi",coverURL:"https://cdn.intechopen.com/books/images_new/11176.jpg",licenceType:"CC BY 3.0",editedByType:null,isbn:"978-1-80355-493-8",printIsbn:"978-1-80355-492-1",pdfIsbn:"978-1-80355-494-5",isAvailableForWebshopOrdering:!0,editors:[{id:"18593",title:"Prof.",name:"Karam",middleName:"Youssef",surname:"Maalawi",slug:"karam-maalawi",fullName:"Karam Maalawi"}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"}},authors:null,sections:[{id:"sec_1",title:"1. Introduction",level:"1"},{id:"sec_2",title:"2. Aerodynamics, electrical, and drive train modeling",level:"1"},{id:"sec_2_2",title:"2.1 Aerodynamics modeling",level:"2"},{id:"sec_3_2",title:"2.2 Electrical modeling",level:"2"},{id:"sec_4_2",title:"2.3 Drive train model",level:"2"},{id:"sec_6",title:"3. Control system",level:"1"},{id:"sec_6_2",title:"3.1 Conventional wind power control scheme",level:"2"},{id:"sec_7_2",title:"3.2 Maximum power point control",level:"2"},{id:"sec_8_2",title:"3.3 Rotor side control",level:"2"},{id:"sec_9_2",title:"3.4 Grid side control",level:"2"},{id:"sec_11",title:"4. Simulation and discussion",level:"1"},{id:"sec_11_2",title:"4.1 Steady-state simulation",level:"2"},{id:"sec_11_3",title:"4.1.1 Steady-state simulation results and analysis",level:"3"},{id:"sec_12_3",title:"Table 1",level:"3"},{id:"sec_13_3",title:"4.1.3 Simulation model of DFIG using wind turbine MPPT block",level:"3"},{id:"sec_16",title:"5. Conclusions",level:"1"},{id:"sec_17",title:"Acknowledgments",level:"1"},{id:"sec_19",title:"Abbreviations",level:"1"}],chapterReferences:[{id:"B1",body:'India Energy Outlook. India Energy Outlook 2021 – Analysis - IEA. India Energy Outlook, 2021'},{id:"B2",body:'Renewable I and Agency E. Renewable Energy Statistics 2021. 2021'},{id:"B3",body:'European Wind Energy Association and Greenpeace. WIND FORCE 12 a blueprint to achieve 12% of the world’s electricity from wind power by 2020. Wind Force. 2005;12(June 2005):1-52'},{id:"B4",body:'Dr P, Li M. World energy 2017-2050: Annual report. World Energy Reports. 2017;(June):1-29'},{id:"B5",body:'Scholtz L, Muluadzi K, Kritzinger K, Mabaso M & Forder S. Renewable Energy: Facts and Futures - The energy future we want. 2017'},{id:"B6",body:'AbdElhafez AA, Alruways SH, Alsaif YA, Althobaiti MF, AlOtaibi AB & Alotaibi NA. Reactive Power Problem and Solutions: An Overview. Journal of Power and Energy Engineering. 2017;5(5):40–54'},{id:"B7",body:'Robert LMT, Gabler E, Petersen JF. Atmospheric pressure, winds, and circulation patterns. Weather. 2008:113-137'},{id:"B8",body:'Wang T. A brief review on wind turbine aerodynamics. Theoretical and Applied Mechanics Letters. 2012;2(6):1-8'},{id:"B9",body:'Ragheb M, Ragheb AM. Wind turbines theory - the Betz equation and optimal rotor tip speed ratio. Intechopen. 2011;1(1):1-22'},{id:"B10",body:'Mcdonald JD, Wojszczyk B, Flynn B, Voloh I. Distribution systems, substations, and integration of distributed generation. In: Encyclopedia of Sustainability Science and Technology. Springer Science+Business Media New York; 2013. pp. 1-63'},{id:"B11",body:'Sewchurran S, Davidson IE. Introduction to the south African renewable energy grid code version 2.9 requirements (part III - discussions and conclusions). IEEE AFRICON: Science, Technology and Innovation for Africa. 2017;17(4):1231-1235'},{id:"B12",body:'Jabal Laafou A, Ait Madi A, Addaim A, Intidam A. Dynamic modeling and improved control of a grid-connected DFIG used in wind energy conversion systems. Mathematical Problems in Engineering. 2020;2020(10):1-15'},{id:"B13",body:'Monteiro CP and Da Costa JS. Simulation and Control of a Dfig-based Wind Turbine. Res. gate NECEC. 2020. no. December, p. 9'},{id:"B14",body:'Boukili Y, Aguiar AP, Carvalho A. A DFIG-based wind turbine operation under balanced and unbalanced grid voltage conditions. IFAC-PapersOnLine. 2020;53(2):12835-12840'},{id:"B15",body:'Akrama K, Xiao Ming H, Mohamed AK, and Paul B. Doubly Fed Induction Generator Open Stator Synchronized Control during Unbalanced Grid Voltage Condition. 2020;13(3155):1-13'},{id:"B16",body:'Eltamaly AM, Al-Saud M, Sayed K, Abo-Khalil AG. Sensorless active and reactive control for DFIG wind turbines using opposition-based learning technique. Sustain. 2020;12(9):1-14'},{id:"B17",body:'Slootweg JG, Polinder H, Kling W. Dynamic modelling of a wind turbine with doubly fed induction generator. IEEE Power Engineering Society Transmission and Distribution Conference. 2001;01(9):644-649'},{id:"B18",body:'Singh M. Dynamic Models for Wind Turbines and Wind Power Plants. 2011'},{id:"B19",body:'Abo-Khalil AG. Modeling and Control Aspects of Wind Power Systems. Impacts of wind farms on power system stability. Wind Power In Power System. 2013:133-151'},{id:"B20",body:'Zhang Y, Zhang L, Liu Y. Implementation of maximum power point tracking based on variable speed forecasting for wind. PRO. 2019;158(7):1-18'},{id:"B21",body:'Jonathan Fournier. Modeling, Control and Experimental Validation of a DFIG-based wind Turbine test bench. Universitat Politecnica de Catalunya, Barcelona, Catalonia Institute for Energy Research (IREC). 2013'},{id:"B22",body:'Badreldien M, Usama R, El-wakeel A, Abdelaziz AY. Modeling, Analysis, and Control of Doubly Fed Induction Generators for Wind Turbines. ICEENG Conference ICEENG-9. 2014:1-18'},{id:"B23",body:'Arnaltes S, Rodriguez-Amenedo JL, Montilla-D Jesus ME. Control of variable speed wind turbines with doubly fed asynchronous generators for stand-alone applications. Energies. 2018;26(11):1-16'},{id:"B24",body:'Soriano LA, Yu W, Rubio JDJ. Modeling and control of wind turbine. Mathematical Problems in Engineering. 2013;2013:1-13'},{id:"B25",body:'Prabakar K. Gain Tuning of Proportional-Integral Controller Based on Multiobjective Optimization and Controller Hardware-in-loop Microgrid set up. 2015'},{id:"B26",body:'Michalke G, Hansen AD, Hartkopf T. Control strategy of a variable speed wind turbine with multipole permanent magnet synchronous generator. European Wind Energy Conference and Exhibition. 2007:1371-1378'},{id:"B27",body:'Abad G, Lopez J, Rodriguez M, Marroyo L, Iwanski G. Doubly Fed Induction Machine. 2011th ed. Hoboken, New Jersey, Wiley Publication: John Wiley & Sons, Inc.; 2011'}],footnotes:[],contributors:[{corresp:"yes",contributorFullName:"Ramesh Kumar Behara",address:"bramesh250770@gmail.com",affiliation:'
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Ansari"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"780",title:"Proteomics",subtitle:"Human Diseases and Protein Functions",isOpenForSubmission:!1,hash:"a90c4e5b369d27036134a3c66ce1cb26",slug:"proteomics-human-diseases-and-protein-functions",bookSignature:"Tsz-Kwong Man and Ricardo J. Flores",coverURL:"https://cdn.intechopen.com/books/images_new/780.jpg",editedByType:"Edited by",editors:[{id:"35047",title:"Prof.",name:"Tsz Kwong",middleName:null,surname:"Man",slug:"tsz-kwong-man",fullName:"Tsz Kwong Man"}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}}],booksByTopicTotal:8,seriesByTopicCollection:[],seriesByTopicTotal:0,mostCitedChapters:[{id:"28196",doi:"10.5772/31776",title:"Exploring the Role of Biomarkers for the Diagnosis and Management of Traumatic Brain Injury Patients",slug:"exploring-the-role-of-biomarkers-for-the-diagnosis-and-management-of-traumatic-brain-injury-patients",totalDownloads:2921,totalCrossrefCites:9,totalDimensionsCites:22,abstract:null,book:{id:"780",slug:"proteomics-human-diseases-and-protein-functions",title:"Proteomics",fullTitle:"Proteomics - Human Diseases and Protein Functions"},signatures:"Linda Papa",authors:[{id:"88648",title:"Dr.",name:"Linda",middleName:null,surname:"Papa",slug:"linda-papa",fullName:"Linda Papa"}]},{id:"66145",doi:"10.5772/intechopen.83426",title:"New Insights into the Mechanisms Underlying NEDD8 Structural and Functional Specificities",slug:"new-insights-into-the-mechanisms-underlying-nedd8-structural-and-functional-specificities",totalDownloads:979,totalCrossrefCites:6,totalDimensionsCites:9,abstract:"Ubiquitin (Ub) and ubiquitin-like (Ubl) proteins are small polypeptides that are conjugated to substrates affecting their activity and stability. Cells encode “receptors” containing Ub-/Ubl-binding domains that interpret and translate each modification into appropriate cellular responses. Among the different Ubls, NEDD8, which is the ubiquitin’s closest relative, retains many of the structural determinants that enable ubiquitin the ability to target proteins to degradation. Nevertheless, the direct involvement of NEDD8 conjugation to proteasome recruitment has been proved only in a few cases. To date, well-defined major NEDD8 substrates are primarily members of the cullin family, and cullin neddylation does not appear to mark these proteins for degradation. Various studies have demonstrated that selectivity between ubiquitin and NEDD8 is guaranteed by small but substantial differences. Nevertheless, several issues still need to be addressed, mainly concerning which interaction surfaces mediate NEDD8 function and what domains recognize them. Recently, two novel domains identified in KHNYN and N4BP1 proteins have shed new light on this research area. Here, I discuss some recent reports that contributed to shed light on the mechanisms underlining the discrimination between ubiquitin and NEDD8. Understanding the details of these molecular mechanisms represents a prominent facet for the identification of new therapeutic targets.",book:{id:"8301",slug:"ubiquitin-proteasome-system-current-insights-into-mechanism-cellular-regulation-and-disease",title:"Ubiquitin Proteasome System",fullTitle:"Ubiquitin Proteasome System - Current Insights into Mechanism Cellular Regulation and Disease"},signatures:"Elena Santonico",authors:[{id:"271923",title:"Dr.",name:"Elena",middleName:null,surname:"Santonico",slug:"elena-santonico",fullName:"Elena Santonico"}]},{id:"28199",doi:"10.5772/31082",title:"F0F1 ATP Synthase: A Fascinating Challenge for Proteomics",slug:"f0f1-atp-synthase-a-fascinating-challenge-for-proteomics",totalDownloads:5521,totalCrossrefCites:2,totalDimensionsCites:8,abstract:null,book:{id:"780",slug:"proteomics-human-diseases-and-protein-functions",title:"Proteomics",fullTitle:"Proteomics - Human Diseases and Protein Functions"},signatures:"Federica Dabbeni-Sala, Amit Kumar Rai and Giovanna Lippe",authors:[{id:"85523",title:"Prof.",name:"Giovanna",middleName:null,surname:"Lippe",slug:"giovanna-lippe",fullName:"Giovanna Lippe"},{id:"149272",title:"Dr.",name:"Federica",middleName:null,surname:"Dabbeni-Sala",slug:"federica-dabbeni-sala",fullName:"Federica Dabbeni-Sala"},{id:"149273",title:"Dr.",name:"Amit",middleName:null,surname:"Kumar Rai",slug:"amit-kumar-rai",fullName:"Amit Kumar Rai"}]},{id:"65025",doi:"10.5772/intechopen.82883",title:"E3 Ubiquitin Ligases in Cancer and Their Pharmacological Targeting",slug:"e3-ubiquitin-ligases-in-cancer-and-their-pharmacological-targeting",totalDownloads:1658,totalCrossrefCites:2,totalDimensionsCites:8,abstract:"Ubiquitination plays many critical roles in protein function and regulation. Consequently, mutation and aberrant expression of E3 ubiquitin ligases can drive cancer progression. Identifying key ligase-substrate relationships is crucial to understanding the molecular basis and pathways behind cancer and toward identifying novel targets for cancer therapeutics. Here, we review the importance of E3 ligases in the regulating the hallmarks of cancer, discuss some of the key and novel E3 ubiquitin ligases that drive tumor formation and angiogenesis, and review the clinical development of inhibitors that antagonize their function. We conclude with perspectives on the field and future directions toward understanding ubiquitination and cancer progression.",book:{id:"8301",slug:"ubiquitin-proteasome-system-current-insights-into-mechanism-cellular-regulation-and-disease",title:"Ubiquitin Proteasome System",fullTitle:"Ubiquitin Proteasome System - Current Insights into Mechanism Cellular Regulation and Disease"},signatures:"Joseph Y. Ong and Jorge Z. Torres",authors:[{id:"186645",title:"Dr.",name:"Jorge",middleName:null,surname:"Torres",slug:"jorge-torres",fullName:"Jorge Torres"},{id:"264944",title:"Mr.",name:"Joseph",middleName:null,surname:"Ong",slug:"joseph-ong",fullName:"Joseph Ong"}]},{id:"57410",doi:"10.5772/intechopen.71404",title:"The Cross Talk among Autophagy, Ubiquitination, and DNA Repair: An Overview",slug:"the-cross-talk-among-autophagy-ubiquitination-and-dna-repair-an-overview",totalDownloads:1215,totalCrossrefCites:2,totalDimensionsCites:4,abstract:"Cellular plasticity is modulated by protein posttranslational modifications, which act on most intracellular pathways. Ubiquitination is a versatile posttranslational modification (PTM) that influences protein fate, controlling their degradation or modulating their activity and subcellular localization. The ubiquitin proteasome system, UPS, and the autophagic pathway are the main degradative intracellular machineries, which rely on ubiquitination for their activation and/or the selective recycling of proteins and organelles. Recent findings indicate that the cross talk between UPS and autophagy plays a key role in controlling DNA repair pathways. Even being a cytoplasmic process, it is now clear that autophagy can directly impact on the correct activation of DNA repair. Of note, defects on autophagy are related to the impairment of homologous recombination repair and to an increase of the nonhomologous end joining repair activity. These evidences give new insights into the molecular processes underlying the DNA damage response and provide further explanation for the tumorigenesis associated with autophagy impairment. Moreover, these findings introduce new examples of synthetic lethality between autophagy and DNA repair genes and lead to the possible development of target therapies for tumors with defective autophagy.",book:{id:"5989",slug:"ubiquitination-governing-dna-repair-implications-in-health-and-disease",title:"Ubiquitination Governing DNA Repair",fullTitle:"Ubiquitination Governing DNA Repair - Implications in Health and Disease"},signatures:"Francesca Nazio, Emiliano Maiani and Francesco Cecconi",authors:[{id:"204392",title:"Prof.",name:"Francesco",middleName:null,surname:"Cecconi",slug:"francesco-cecconi",fullName:"Francesco Cecconi"},{id:"204393",title:"Dr.",name:"Emiliano",middleName:null,surname:"Maiani",slug:"emiliano-maiani",fullName:"Emiliano Maiani"},{id:"204394",title:"Dr.",name:"Francesca",middleName:null,surname:"Nazio",slug:"francesca-nazio",fullName:"Francesca Nazio"}]}],mostDownloadedChaptersLast30Days:[{id:"70577",title:"Proteoforms: General Concepts and Methodological Process for Identification",slug:"proteoforms-general-concepts-and-methodological-process-for-identification",totalDownloads:899,totalCrossrefCites:1,totalDimensionsCites:1,abstract:"The term proteoform is used to denote all the molecular forms in which the protein product of a single gene can be found. The most frequent processes that lead to transcript modification and the biological implications of these changes observed in the final protein product will be discussed. Proteoforms arising from genetic variations, alternatively spliced RNA transcripts and post-translational modifications will be commented. This chapter will present an evolution of the techniques used to identify the proteoforms and the importance of this identification for understanding of biological processes. This chapter highlights the fundamental concepts in the field of top-down mass spectrometry (TDMS), and provides numerous examples for the use of knowledge obtained from the identification of proteoforms. The identification of mutant proteins is one of the emerging areas of proteogenomics and has the potential to recognize novel disease biomarkers and may point to useful targets for identification of therapeutic approaches.",book:{id:"9352",slug:"proteoforms-concept-and-applications-in-medical-sciences",title:"Proteoforms",fullTitle:"Proteoforms - Concept and Applications in Medical Sciences"},signatures:"Jucélia da Silva Araújo and Olga Lima Tavares Machado",authors:[{id:"30130",title:"Dr.",name:"Olga Lima Tavares",middleName:null,surname:"Machado",slug:"olga-lima-tavares-machado",fullName:"Olga Lima Tavares Machado"},{id:"310148",title:"Dr.",name:"Jucelia",middleName:null,surname:"Da Silva Araujo",slug:"jucelia-da-silva-araujo",fullName:"Jucelia Da Silva Araujo"}]},{id:"65025",title:"E3 Ubiquitin Ligases in Cancer and Their Pharmacological Targeting",slug:"e3-ubiquitin-ligases-in-cancer-and-their-pharmacological-targeting",totalDownloads:1658,totalCrossrefCites:2,totalDimensionsCites:8,abstract:"Ubiquitination plays many critical roles in protein function and regulation. Consequently, mutation and aberrant expression of E3 ubiquitin ligases can drive cancer progression. Identifying key ligase-substrate relationships is crucial to understanding the molecular basis and pathways behind cancer and toward identifying novel targets for cancer therapeutics. Here, we review the importance of E3 ligases in the regulating the hallmarks of cancer, discuss some of the key and novel E3 ubiquitin ligases that drive tumor formation and angiogenesis, and review the clinical development of inhibitors that antagonize their function. We conclude with perspectives on the field and future directions toward understanding ubiquitination and cancer progression.",book:{id:"8301",slug:"ubiquitin-proteasome-system-current-insights-into-mechanism-cellular-regulation-and-disease",title:"Ubiquitin Proteasome System",fullTitle:"Ubiquitin Proteasome System - Current Insights into Mechanism Cellular Regulation and Disease"},signatures:"Joseph Y. Ong and Jorge Z. Torres",authors:[{id:"186645",title:"Dr.",name:"Jorge",middleName:null,surname:"Torres",slug:"jorge-torres",fullName:"Jorge Torres"},{id:"264944",title:"Mr.",name:"Joseph",middleName:null,surname:"Ong",slug:"joseph-ong",fullName:"Joseph Ong"}]},{id:"65109",title:"Ubiquitin Signaling in Regulation of the Start of the Cell Cycle",slug:"ubiquitin-signaling-in-regulation-of-the-start-of-the-cell-cycle",totalDownloads:1559,totalCrossrefCites:2,totalDimensionsCites:3,abstract:"The small protein ubiquitin plays a vital role in virtually all aspects of cellular life. Among the diverse signaling outcomes associated with ubiquitination, the most well-established is the targeted degradation of substrates via the proteasome. During cell growth and proliferation, ubiquitin plays an outsized role in promoting progression through the cell cycle. In particular, ubiquitin-mediated degradation is critically important at transition points where it provides directionality and irreversibility to the cell cycle, which is essential for maintaining genome integrity. Specifically, the boundary between G1 and S-phase is tightly regulated by the ubiquitin proteasome system. Notably, the G1/S boundary represents a major barrier to cell proliferation and is universally dysfunctional in cancer cells, allowing for the unbridled proliferation observed in malignancy. Numerous E3 ubiquitin ligases, which facilitate the ubiquitination of specific substrates, have been shown to control G1/S. In this chapter, we will discuss components in the ubiquitin proteasome system that are implicated in G1/S control, how these enzymes are interconnected, gaps in our current knowledge, and the potential role of these pathways in the cancer cycle and disease proliferation.",book:{id:"8301",slug:"ubiquitin-proteasome-system-current-insights-into-mechanism-cellular-regulation-and-disease",title:"Ubiquitin Proteasome System",fullTitle:"Ubiquitin Proteasome System - Current Insights into Mechanism Cellular Regulation and Disease"},signatures:"Michael James Emanuele and Taylor Paige Enrico",authors:[{id:"264977",title:"Dr.",name:"Michael",middleName:null,surname:"Emanuele",slug:"michael-emanuele",fullName:"Michael Emanuele"},{id:"282200",title:"Ms.",name:"Taylor",middleName:null,surname:"Enrico",slug:"taylor-enrico",fullName:"Taylor Enrico"}]},{id:"60432",title:"Protein-Based Detection Methods for Genetically Modified Crops",slug:"protein-based-detection-methods-for-genetically-modified-crops",totalDownloads:1391,totalCrossrefCites:3,totalDimensionsCites:4,abstract:"The generation of genetically modified (GM) crops is rapidly expanding each and every year around the world. The well-being and quality assessment of these harvests are vital issues with respect to buyers’ interests. This drove the administrative specialists to execute an arrangement of extremely strict strategies for the endorsement to develop and use GMOs and to produce an interest in scientific techniques equipped for identifying GM crops. The GM crops have been added to the effective fuse of various attributes by presenting transgenes, for example, Bacillus thuringiensis (Bt) insecticidal qualities, in various crop species. GM crops give critical financial, natural, well-being and social advantages to both small and large agriculturists. The detection strategies incorporate either DNA-based or protein-based measures. Different immunoassays or catalyst connected immunosorbent tests are delicate and more affordable; however, they need experienced technicians. A very simple method, that is, immunochromatographic (ICS) test, is set up in the world, which is modest, compact and simple to utilize. The ICS is a semiquantitative method for indicative screening and semi-measurement of new remote proteins presented through hereditary change of plants. The strip is the easiest method for the assessment of several Bt crop plants for insecticidal quality.",book:{id:"6635",slug:"protein-protein-interaction-assays",title:"Protein-Protein Interaction Assays",fullTitle:"Protein-Protein Interaction Assays"},signatures:"Kausar Malik, Haleema Sadia and Muhammad Hamza Basit",authors:[{id:"238750",title:"Prof.",name:"Kausar",middleName:null,surname:"Malik",slug:"kausar-malik",fullName:"Kausar Malik"},{id:"243713",title:"Dr.",name:"Haleema",middleName:null,surname:"Sadia",slug:"haleema-sadia",fullName:"Haleema Sadia"},{id:"243714",title:"Mr.",name:"Muhammad Hamza",middleName:null,surname:"Basit",slug:"muhammad-hamza-basit",fullName:"Muhammad Hamza Basit"}]},{id:"60064",title:"Rapid Endosomal Recycling",slug:"rapid-endosomal-recycling",totalDownloads:1303,totalCrossrefCites:2,totalDimensionsCites:3,abstract:"Peripheral membrane proteins are endocytosed by constitutive processes of membrane invaginations, followed by internalization driven by diverse endocytic machinery available at the cell surface. It is believed that after endocytic uptake, cargo proteins proceed either through the endosomal recycling circuit of the cell or travel toward late endosomes for degradation. In this chapter, we analyzed trafficking of seven cargo molecules (transferrin receptor, fully conformed MHC-I, non-conformed MHC-I, cholera-toxin B subunit, CD44, ICAM1, and G-protein-coupled receptor Rae-1) known to use the distinct endocytic route. For that purpose, we developed the software for multicompartment analysis of intracellular trafficking. 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Yet, overexpression at bacterial systems with recombinant modifications brings further difficulties. Adding a tag, an affinity label, and expressing particular domains of the whole protein, especially hydrophobic sections, make purification a challenging process. Protein folding pattern may perturb N- or C-terminal tag and this terminal preference may lead to poor purification yield. Codon optimization, solvent content and type, ionic conditions, resin types, and self-cleavage of recombinant proteins bring further difficulties to protein expression and purification steps. The chapter overviews problems of protein purification through a small peptide overexpression in bacteria (Recombinant anti-SARS Coronavirus 2 (SARS-Cov-2) Spike protein Receptor Binding Domain (RBD) antibody (Clone Sb#14). 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Protein-related diseases include proteopathies (proteinopathies) such as neurodegenerative diseases and metabolic disorders like protein-energy malnutrition and some hormonopathies. Hormonopathies are associated with the change in the production of hormones. Diabetes mellitus, a type of hormonopathy, is reviewed in this work alongside neurodegenerative diseases and protein-energy malnutrition. This chapter aims to elucidate more on the diagnosis of these diseases considering the structure and function of their proteins viz-a-viz their deficiencies and hyper-production in man. Their pathogenesis and the principles underlying their diagnosis are further discussed to optimize the management of these diseases among patients.",book:{id:"10839",title:"Protein Detection",coverURL:"https://cdn.intechopen.com/books/images_new/10839.jpg"},signatures:"Ohanube A.K. Goodluck, Obeta M. Uchejeso and Ikeagwulonu R. 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Saxena is a vice dean and professor at King George's Medical University, Lucknow, India. His research interests involve understanding the molecular mechanisms of host defense during human viral infections and developing new predictive, preventive, and therapeutic strategies for them using Japanese encephalitis virus (JEV), HIV, and emerging viruses as a model via stem cell and cell culture technologies. His research work has been published in various high-impact factor journals (Science, PNAS, Nature Medicine) with a high number of citations. He has received many awards and honors in India and abroad including various Young Scientist Awards, BBSRC India Partnering Award, and Dr. JC Bose National Award of Department of Biotechnology, Min. of Science and Technology, Govt. of India. Dr. Saxena is a fellow of various international societies/academies including the Royal College of Pathologists, United Kingdom; Royal Society of Medicine, London; Royal Society of Biology, United Kingdom; Royal Society of Chemistry, London; and Academy of Translational Medicine Professionals, Austria. He was named a Global Leader in Science by The Scientist. He is also an international opinion leader/expert in vaccination for Japanese encephalitis by IPIC (UK).",institutionString:null,institution:{name:"King George's Medical University",institutionURL:null,country:{name:"India"}}}]},{type:"book",id:"7123",title:"Current Topics in Neglected Tropical Diseases",subtitle:null,coverURL:"https://cdn.intechopen.com/books/images_new/7123.jpg",slug:"current-topics-in-neglected-tropical-diseases",publishedDate:"December 4th 2019",editedByType:"Edited by",bookSignature:"Alfonso J. 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Since then, he has been working as an Adjunct Professor in the same Department at the University of Pavia. His research activity during the first years was primarily focused on the purification and structural characterization of enzymes from animal and plant sources. During this period, Prof. Iadarola familiarized himself with the conventional techniques used in column chromatography, spectrophotometry, manual Edman degradation, and electrophoresis). Since 1995, he has been working on: i) the determination in biological fluids (serum, urine, bronchoalveolar lavage, sputum) of proteolytic activities involved in the degradation processes of connective tissue matrix, and ii) on the identification of biological markers of lung diseases. In this context, he has developed and validated new methodologies (e.g., Capillary Electrophoresis coupled to Laser-Induced Fluorescence, CE-LIF) whose application enabled him to determine both the amounts of biochemical markers (Desmosines) in urine/serum of patients affected by Chronic Obstructive Pulmonary Disease (COPD) and the activity of proteolytic enzymes (Human Neutrophil Elastase, Cathepsin G, Pseudomonas aeruginosa elastase) in sputa of these patients. More recently, Prof. Iadarola was involved in developing techniques such as two-dimensional electrophoresis coupled to liquid chromatography/mass spectrometry (2DE-LC/MS) for the proteomic analysis of biological fluids aimed at the identification of potential biomarkers of different lung diseases. He is the author of about 150 publications (According to Scopus: H-Index: 23; Total citations: 1568- According to WOS: H-Index: 20; Total Citations: 1296) of peer-reviewed international journals. 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Biochemistry examines macromolecules - proteins, nucleic acids, carbohydrates, and lipids – and their building blocks, structures, functions, and interactions. Much of biochemistry is devoted to enzymes, proteins that catalyze chemical reactions, enzyme structures, mechanisms of action and their roles within cells. Biochemistry also studies small signaling molecules, coenzymes, inhibitors, vitamins, and hormones, which play roles in life processes. Biochemical experimentation, besides coopting classical chemistry methods, e.g., chromatography, adopted new techniques, e.g., X-ray diffraction, electron microscopy, NMR, radioisotopes, and developed sophisticated microbial genetic tools, e.g., auxotroph mutants and their revertants, fermentation, etc. More recently, biochemistry embraced the ‘big data’ omics systems. Initial biochemical studies have been exclusively analytic: dissecting, purifying, and examining individual components of a biological system; in the apt words of Efraim Racker (1913 –1991), “Don’t waste clean thinking on dirty enzymes.” Today, however, biochemistry is becoming more agglomerative and comprehensive, setting out to integrate and describe entirely particular biological systems. The ‘big data’ metabolomics can define the complement of small molecules, e.g., in a soil or biofilm sample; proteomics can distinguish all the comprising proteins, e.g., serum; metagenomics can identify all the genes in a complex environment, e.g., the bovine rumen. 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Dr. Blumenberg’s research is focused on the epidermis, expression of keratin genes, transcription profiling, keratinocyte differentiation, inflammatory diseases and cancers, and most recently the effects of the microbiome on the skin. 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