Preprint
Article

This version is not peer-reviewed.

Comparative Analysis of Tri-Polar Concentric Ring and Conventional Electrodes for Overt and Covert Speech

Submitted:

20 May 2026

Posted:

21 May 2026

You are already at the latest version

Abstract
Brain-Computer Interface (BCI) is a system that enables the human brain to interact with the external environment without using muscles. Electroencephalography (EEG) is a commonly used modality for measuring neural brain activity. However, its low signal-to-noise ratio (SNR) and electrode reference problems lead to poor spatial resolution. As a result, EEG signals are often contaminated with physiological artifacts such as muscle movements. Therefore, this study used novel tripolar concentric ring electrodes (TCREs) that are used to record brain activity related to the overt and covert speech. Brain signals associated with overt and covert speech were recorded using TCREs and disc electrodes. Classification algorithms, including K-Nearest Neighbors (KNN), Fully Connected Neural Networks (FCNNN), and Convolutional Neural Networks (CNN), were used to classify the TCRE and conventional EEG signals. The data was collected from 16 healthy participants. The experimental results demonstrate that TCREs provide superior performance compared to conventional disc electrodes. In addition to that, the 0.5–1.2s interval, corresponding to the peak stimulus window, exhibits a maximum power of 250µV. The average accuracy achieved during this epoch was 86.25%, whereas the remaining epoch shows an accuracy of 83.5% using TCREs.
Keywords: 
;  ;  ;  ;  ;  ;  ;  ;  ;  

1. Introduction

The Brain–Computer Interface (BCI) is a system that enables direct communication between the brain and external devices [1]. These systems enable individuals with motor impairments to perform everyday tasks and interact with the external environment [2]. There are a number of signals that are used in BCI, such as electromyography (EMG) [3], functional magnetic resonance imaging (fMRI) [4], magnetoencephalography (MEG) [5], electroencephalography (EEG) [6], and electrocorticography (ECoG) [7].
Among these signals, EEG and ECoG are commonly used in BCI as these signals reflect the electrical response of the brain. ECoG studies require surgery to insert electrodes in the human brain [8]. On the other hand, scalp EEG is one of the most popular modalities of BCI systems because it is non-invasive and does not require surgery to insert electrodes in the brain. However, there are some limitations of EEG electrodes, such as spatial resolution, signal contamination, and the reference electrode problem [9,10]. Therefore, there is a need for new types of electrodes, such as Tripolar Concentric Ring Electrode (TCRE) that can attenuate the dependency of reference electrodes, signal contamination, and muscle artifacts. The TCRE are developed using three rings that calculate the Surface Laplacian (SL) directly on the hardware of TCRE. The SL works as a high pass filter that enhances the spatial resolution and reduces the reference electrode problem [11]. This helps to extract the more distinctive features of the EEG. Figure 1 presents the structural difference between conventional disc and TCRE electrodes.
In the last few decades, BCI research has been explored in large parts of the human body such as elbows [12], wrists [13], legs [14], tongue [15], and upper limbs [16]. Limited research has been done on the overt (aloud) and covert (silent) behavior of the brain. Overt and covert brain signals are very critical to understand because they help people who suffer from aphasia or speech impairment injuries and are unable to communicate with the outside world. Therefore, this study focuses on the overt and covert behavior of the brain. Machine learning and deep learning will be used to analyze the overt and covert data which are recorded through conventional and TCRE electrodes.
The main contributions discussed in this paper are: (i) a comparative evaluation of TCRE and conventional disc electrodes for EEG-based Overt and covert speech discrimination; (ii) investigation of machine learning and deep learning models to differentiate overt and covert signals.
This paper consists of (i) an introduction which explains the EEG signals; (ii) related work that elaborates the recent work done on overt/covert speech, electrode types, and machine learning or deep learning models; (iii) methodology, which explains the flow of the research study; (iv) results and discussion show the output of conventional and TCRE electrodes and overt and covert speech differentiation; (v) conclusion of the paper; (vi) future work.

3. Methodology

This study aims to classify conventional disc electrodes and TCRE signals based on overt and covert speech data. Figure 2 represents the methodology of the experiment carried out in this study.

3.1. EEG Data Acquisition

In this study, EEG data were recorded using both TCRE and disc electrodes. The image was shown on the computer screen and the participant was instructed to speak loudly the name of the image within 2.5 seconds, followed by 3.5 seconds break time. For the covert experiment, the participant was asked to silently imagine the name of the image shown on the screen.TCRE and disc electrodes were placed on the scalp to concurrently record the EEG signals.

3.1.1. Participants

Data were obtained from 16 healthy participants. It is observed that there is high variability between the participant data and inter-trial variability within the same participant’s EEG signals [29]. Data for this article were recorded in the Neural Rehabilitation Lab at the University of Rhode Island (URI). Before the experiment, all participants provided their consent, which was approved by the URI’s Institutional Review Board (IRB). Each participant performed two runs: overt and covert. Each run recorded 100 trials. In total, 200 trials were recorded for each participant, with overt and covert trials interspersed.

3.1.2. Experimental Naming Paradigm

The following picture naming paradigm was performed. Participants were presented a random image and asked to speak loudly the name of that picture and also imagine silently the name of the same picture. Each image stimulus was shown for 3500 milliseconds, followed by a 2500 milliseconds for the participant to speak overtly or covertly the name of the image. The EEG data were sampled at a rate of 1000 samples per second. The impedance was maintained below 10K Ω . The 10-20 International Electrode Positioning System was referenced to place both TCRE and conventional electrodes. Data were recorded using 5, 7, and 8 electrodes placed on the front and parietal parts of both left and right hemispheres.

3.2. Signal Preprocessing

The raw EEG signals contain noise and artifacts such as eye blink, muscle movements, body posture, etc. The band-pass filter was used to improve signal quality and data was extracted between 1 Hz and 40 Hz to remove low and high frequency signals which also include power-line signals [30]. Therefore, pre-processing is necessary to preserve neural activity while minimizing irrelevant signals.

3.3. Epoch Extraction

Once the pre-processing step was done, the EEG signals were segmented into epochs. Each epoch represents the neural activity within a time window that follows the stimulus. The signal was separated peak Vs. non-peak stimuli, where peak refers to time interval with higher EEG amplitude and non-peak represents the lower activity period.

3.4. TCRE and Disc Electrodes Separation

Data were recorded using TCRE and disc electrodes at the same time at the same region of the brain according to the 10-20 montage to analyze the signals from both electrode types. Signals from disc electrodes were obtained from the outer ring of a TCRE. The EEG signals exhibit a maximum power of 60 μ V throughout the entire segmented epoch, while TCRE shows fluctuation, which separated both signals from each other.

3.5. Time–Frequency Analysis

The EEG signals are non-stationary with changes in frequency and time. This requires a time-frequency analysis to represent the EEG signals [31]. In this paper, the Morlet wavelet transform was used to analyze the temporal evaluation of the signal with frequency. This Morlet Wavelet transform provides the baseline for the EEG signal [32]. It helps to extract the discriminative feature of overt and covert speech.

3.6. Classification Models

The classification algorithms are used to evaluate the TCRE and conventional disc electrodes signals and also to classify overt versus covert performance. The KNN, CNN, and FCNN will be used to classify the signals from TCRE and conventional disc electrodes. These classification algorithms will be evaluated separately.

3.7. Performance Evaluation

To ensure the performance of the classification algorithms, 5-fold cross validation will be performed. This can reduce the overfitting problem [33]. The final performance of the model was evaluated using the accuracy and confusion matrices.

4. Results and Discussion

In this section, the results of EEG-based speech experiment using TCRE and conventional electrodes will be explained.

4.1. Overall Performance Comparison

The overall performance will be compared between TCRE and disc electrodes. The classification algorithms such as KNN, FCNNN, and CNN will be used to analyze data capture from both TCRE and disc electrodes. Data were divided into 80% training and 20% testing data. The 5-fold cross validation was performed to partition the training data and validation set. The validation set was used in each cycle during the training phase. Once the ML model is trained, testing data was given to the model to check its robustness. Table 2 shows the results of testing data, which were not seen during the training phase.
The results of three participants will be discussed: one which has lowest accuracy in all algorithms, another which has highest accuracy, and the third which has average accuracy in almost all classification algorithms.
Among all the classification algorithms used in this study, KNN shows the highest accuracy for many participant results. Participant 01 shows the accuracy of 55.0% using TCRE and 50.0% using disc electrodes. Participant 11 represents the accuracy of 97.5% with TCRE and 77.5% with disc electrodes. Participant 16 shows the accuracy of 97.5% using both TCRE and disc electrodes.
The performance of classification algorithms varies among participants and no single algorithm consistently outperforms in all the participants. In addition to that, the electrode type also influences the performance of classification algorithms. These findings suggest that the electrode selection and classification algorithm plays an important role in the differentiation of overt versus covert EEG-speech. The results calculated using TCRE electrodes shows the enhanced signal quality and separability of neural patterns associated with overt and covert speech.

4.2. TCRE vs. Disc Electrode Analysis

Figure 3 illustrate the distribution of test data accuracies for the KNN, FCNN, and CNN classifiers using TCRE and disc electrodes. The TCRE based classifiers exhibit higher accuracy compared to the disc electrode classifiers. Among the classifiers, CNN with TCRE showed a higher median accuracy with more data points observed in the upper range. KNN exhibits competitive performance with TCRE but shows a reduction in accuracy and increased variability using disc electrodes. However, FCNN shows lower accuracy but it is more consistent in both electrode types. The observed variability in the results shows that the performance of the classification algorithm differs among the participants and is influenced by the electrode type.

4.3. Classifier Performance Analysis

The classification algorithms such as KNN, FCNNN, and CNN were evaluated using confusion matrices to see the performance of classification algorithms. The confusion matrices are shown in the Figure 4, Figure 5 and Figure 6. It is observed that KNN consistently achieved higher results compared to CNN and FCNNN. This can be attributed to the KNN’s ability to capture more localized neural EEG signals. CNN also illustrates strong performance especially TCRE captured data. In contrast, FCNN represents a relatively lower performance. This represents its limited ability to capture spatiotemporal EEG patterns. These results suggest the importance of selecting the classification algorithms for EEG-based overt/covert differentiation.

4.4. Epoch Segmentation and Analysis

In this section, we examine the time duration of the epoch (0 - 2.5 seconds). For analysis purposes, a participant was taken from the overt and covert data set to investigate the variation in the epoch over time. Figure 7 represents the overt and covert EEG signals of Participant 11. Each epoch comprises of two parts: peak and non-peak. Peak is the amplitude of signals over the time when the participant speaks aloud(overt) or silently imagines (covert) the name of the image shown on the computer to record the brain activity. The non-peak refers to the neural activity recorded before and after the peak activity. Each epoch represents the average response of 200 runs that were collected for a single participant.
Figure 8 exhibits the confusion matrix for classification algorithm KNN on data from participant 11. The overt data are correctly classified at a rate of 68.2% while experiencing a mis-classification rate of 31.8%. In contrast, covert data are correctly classified with an accuracy of 94.4%, with a mis-classification rate of 5.6%. On the other hand, at non-peak intervals of the epoch, overt and covert runs are correctly classified at a rate of 75%, with a mis-classifcation rate of 25% for both overt and covert runs.

5. Conclusion

This study focused on the analysis of EEG data recorded during overt and covert speech using both TCRE and disc electrodes. Different classification algorithms such as KNN, FCNN, and CNN were used to differentiate between overt and covert speech. The results suggest that TCRE based EEG more consistently improves the classification performance compared to the disc electrodes. Among the classification algorithms, KNN captures more EEG neural patterns, while CNN also exhibited strong performance. On the other hand, FCNN shows comparatively lower performance in both electrode types.
In addition to that, the analysis of epoch segments show that the peak interval, which represents the strong neural activity during overt and covert speech task, contain more discriminative information than non-peak intervals. The classification results showed that the higher accuracy of covert during peak segment shows the potential of the EEG signals to capture a more subtle neural pattern associated with imagined speech. The findings illustrate that the electrode type plays a very important role in capturing the EEG data. The TCRE results suggest its potential to be used as an alternative to conventional disc electrodes for non-invasive BCI.

6. Future Work

Future work will focus on improving the TCRE design and exploring new channel configurations to capture EEG data. In addition to that, advanced classification algorithms and larger data sets will be used to improve the robustness of EEG-based overt and covert speech systems.

Acknowledgments

The authors express sincere gratitude to the Neural Rehabilitation Lab at the University of Rhode Island (URI) for providing the EEG data set and also the development of novel electrodes, which form the core contribution of this study. The authors also thank all subjects who voluntarily helped record the data and helped in the data collection process.

Abbreviations

The abbreviations used in this manuscript are these:
BCI Brain Computer Interface
EEG Electroencephalography
ECoG Electrocorticography
EMG Electromyography
fMRI Functional Magnetic Resonance Imaging
MEG Magnetoencephalography
TCRE Tripolar Concentric Ring Electrode
KNN K-Nearest Neighbors
FCNNN Fully Connected Neural Network
CNN Convolutional Neural Network
SNR Signal toNoise Ratio
HFO High Frequency Oscillation

References

  1. Lotte, F.; Bougrain, L.; Cichocki, A.; Clerc, M.; Congedo, M.; Rakotomamonjy, A.; Yger, F. A review of classification algorithms for EEG-based brain–computer interfaces: a 10 year update. J. Neural Eng. 2018, 15, 031005. [Google Scholar] [CrossRef]
  2. Liao, K.; Xiao, R.; Gonzalez, J.; Ding, L. Decoding individual finger movements from one hand using human EEG signals. PLoS ONE 2014, 9, e85192. [Google Scholar] [CrossRef] [PubMed]
  3. Boostani, R.; Moradi, M.H. Evaluation of the forearm EMG signal features for the control of a prosthetic hand. Physiol. Meas. 2003, 24, 309. [Google Scholar] [CrossRef]
  4. Sitaram, R.; Caria, A.; Veit, R.; Gaber, T.; Rota, G.; Kuebler, A.; Birbaumer, N. FMRI brain-computer interface: a tool for neuroscientific research and treatment. Comput. Intell. Neurosci. 2007, 2007, 1. [Google Scholar] [CrossRef]
  5. Bradberry, T.J.; Rong, F.; Contreras-Vidal, J.L. Decoding center-out hand velocity from MEG signals during visuomotor adaptation. Neuroimage 2009, 47, 1691–1700. [Google Scholar] [CrossRef]
  6. Bradberry, T.J.; Gentili, R.J.; Contreras-Vidal, J.L. Reconstructing three-dimensional hand movements from noninvasive electroencephalographic signals. J. Neurosci. 2010, 30, 3432–3437. [Google Scholar] [CrossRef]
  7. Pistohl, T.; Schulze-Bonhage, A.; Aertsen, A.; Mehring, C.; Ball, T. Decoding natural grasp types from human ECoG. Neuroimage 2012, 59, 248–260. [Google Scholar] [CrossRef]
  8. Schalk, G.; Kubanek, J.; Miller, K.; Anderson, N.; Leuthardt, E.; Ojemann, J.; Limbrick, D.; Moran, D.; Gerhardt, L.; Wolpaw, J. Decoding two-dimensional movement trajectories using electrocorticographic signals in humans. J. Neural Eng. 2007, 4, 264. [Google Scholar] [CrossRef] [PubMed]
  9. Babiloni, F.; Babiloni, C.; Fattorini, L.; Carducci, F.; Onorati, P.; Urbano, A. Performances of surface Laplacian estimators: a study of simulated and real scalp potential distributions. Brain Topogr. 1995, 8, 35–45. [Google Scholar] [CrossRef]
  10. Besio, W.G.; Martínez-Juárez, I.E.; Makeyev, O.; Gaitanis, J.N.; Blum, A.S.; Fisher, R.S.; Medvedev, A.V. High-frequency oscillations recorded on the scalp of patients with epilepsy using tripolar concentric ring electrodes. IEEE J. Transl. Eng. Health Med. 2014, 2. [Google Scholar] [CrossRef] [PubMed]
  11. Makeyev, O.; Ding, Q.; Besio, W.G. Improving the accuracy of Laplacian estimation with novel multipolar concentric ring electrodes. Measurement 2016, 80, 44–52. [Google Scholar] [CrossRef]
  12. Zhou, J.; Yao, J.; Deng, J.; Dewald, J.P. EEG-based classification for elbow versus shoulder torque intentions involving stroke subjects. Comput. Biol. Med. 2009, 39, 443–452. [Google Scholar] [CrossRef]
  13. Gu, Y.; Dremstrup, K.; Farina, D. Single-trial discrimination of type and speed of wrist movements from EEG recordings. Clin. Neurophysiol. 2009, 120, 1596–1600. [Google Scholar] [CrossRef]
  14. Pfurtscheller, G.; Brunner, C.; Schlögl, A.; Da Silva, F.L. Mu rhythm (de) synchronization and EEG single-trial classification of different motor imagery tasks. NeuroImage 2006, 31, 153–159. [Google Scholar] [CrossRef] [PubMed]
  15. Morash, V.; Bai, O.; Furlani, S.; Lin, P.; Hallett, M. Classifying EEG signals preceding right hand, left hand, tongue, and right foot movements and motor imageries. Clin. Neurophysiol. 2008, 119, 2570–2578. [Google Scholar] [CrossRef]
  16. Doud, A.J.; Lucas, J.P.; Pisansky, M.T.; He, B. Continuous three-dimensional control of a virtual helicopter using a motor imagery based brain-computer interface. PLoS ONE 2011, 6, e26322. [Google Scholar] [CrossRef] [PubMed]
  17. Hossain, A.; Ovi, T.H.; Mahmood, M.A.I.; Kader, M.F. Classification of Envisioned English Speech from EEG using deep learning approaches. Mach. Learn. With Appl. 2025, 22, 100752. [Google Scholar] [CrossRef]
  18. Jiang, M.; Ding, Y.; Zhang, W.; Teo, K.A.C.; Fong, L.; Zhang, S.; Guo, Z.; Liu, C.; Bhuvanakantham, R.; Sim, W.K.J.; et al. Decoding covert speech from EEG using a functional areas spatio-temporal transformer. arXiv 2025, arXiv:2504.03762. [Google Scholar] [CrossRef]
  19. Milyani, A.H.; Attar, E.T. Deep learning for inner speech recognition: a pilot comparative study of EEGNet and a spectro-temporal Transformer on bimodal EEG-fMRI data. Front. Hum. Neurosci. 2025, 19, 1668935. [Google Scholar] [CrossRef]
  20. Alharbi, Y.F.; Alotaibi, Y.A. Decoding imagined speech from eeg data: A hybrid deep learning approach to capturing spatial and temporal features. Life 2024, 14, 1501. [Google Scholar] [CrossRef] [PubMed]
  21. Abdulghani, M.M.; Walters, W.L.; Abed, K.H. Imagined speech classification using EEG and deep learning. Bioengineering 2023, 10, 649. [Google Scholar] [CrossRef]
  22. Safonova, A.; Ghazaryan, G.; Stiller, S.; Main-Knorn, M.; Nendel, C.; Ryo, M. Ten deep learning techniques to address small data problems with remote sensing. Int. J. Appl. Earth Obs. Geoinf. 2023, 125, 103569. [Google Scholar] [CrossRef]
  23. Besio, G.; Koka, K.; Aakula, R.; Dai, W. Tri-polar concentric ring electrode development for Laplacian electroencephalography. IEEE Trans. Biomed. Eng. 2006, 53, 926–933. [Google Scholar] [CrossRef] [PubMed]
  24. Toole, C.; Martinez-Juárez, I.E.; Gaitanis, J.N.; Blum, A.; Sunderam, S.; Ding, L.; DiCecco, J.; Besio, W.G. Source localization of high-frequency activity in tripolar electroencephalography of patients with epilepsy. Epilepsy Behav. 2019, 101, 106519. [Google Scholar] [CrossRef] [PubMed]
  25. Liu, X.; Makeyev, O.; Besio, W. Improved spatial resolution of electroencephalogram using tripolar concentric ring electrode sensors. J. Sens. 2020, 2020. [Google Scholar] [CrossRef]
  26. Alzahrani, S.I.; Anderson, C.W. A Comparison of Conventional and Tri-Polar EEG Electrodes for Decoding Real and Imaginary Finger Movements from One Hand. Int. J. Neural Syst. 2021, 31, 2150036. [Google Scholar] [CrossRef]
  27. Besio, W.; Koka, K. Mutual Information of Tri-polar Concentric Ring Electrodes. In Proceedings of the 2006 International Conference of the IEEE Engineering in Medicine and Biology Society, 2006; pp. 1106–1109. [Google Scholar]
  28. Koka, K.; Besio, W.G. Improvement of spatial selectivity and decrease of mutual information of tri-polar concentric ring electrodes. J. Neurosci. Methods 2007, 165, 216–222. [Google Scholar] [CrossRef]
  29. García-Salinas, J.S.; Villaseñor-Pineda, L.; Reyes-García, C.A.; Torres-García, A.A. Transfer learning in imagined speech EEG-based BCIs. Biomed. Signal Process. Control 2019, 50, 151–157. [Google Scholar] [CrossRef]
  30. Jiang, X.; Bian, G.B.; Tian, Z. Removal of artifacts from EEG signals: a review. Sensors 2019, 19, 987. [Google Scholar] [CrossRef]
  31. Morales, S.; Bowers, M.E. Time-frequency analysis methods and their application in developmental EEG data. Dev. Cogn. Neurosci. 2022, 54, 101067. [Google Scholar] [CrossRef]
  32. Cohen, M.X. A better way to define and describe Morlet wavelets for time-frequency analysis. NeuroImage 2019, 199, 81–86. [Google Scholar] [CrossRef] [PubMed]
  33. Kramer, O. Dimensionality reduction with unsupervised nearest neighbors; Springer, 2013; Vol. 51. [Google Scholar]
Figure 1. Structural difference between conventional disc electrodes and TCRE.
Figure 1. Structural difference between conventional disc electrodes and TCRE.
Preprints 214601 g001
Figure 2. Overview of classification of TCRE and conventional electrodes EEG signal recorded using over/covert speech.
Figure 2. Overview of classification of TCRE and conventional electrodes EEG signal recorded using over/covert speech.
Preprints 214601 g002
Figure 3. All participants classifiers’ results.
Figure 3. All participants classifiers’ results.
Preprints 214601 g003
Figure 4. Confusion matrix of TCRE and disc electrodes using KNN.
Figure 4. Confusion matrix of TCRE and disc electrodes using KNN.
Preprints 214601 g004
Figure 5. Confusion matrix of TCRE and disc electrodes using FCNNN.
Figure 5. Confusion matrix of TCRE and disc electrodes using FCNNN.
Preprints 214601 g005
Figure 6. Confusion matrix of TCRE and disc electrodes using CNN.
Figure 6. Confusion matrix of TCRE and disc electrodes using CNN.
Preprints 214601 g006
Figure 7. Participant 11 - Analysis of peak epoch between (0.5-1.2) Vs. remaining non-peak epoch.
Figure 7. Participant 11 - Analysis of peak epoch between (0.5-1.2) Vs. remaining non-peak epoch.
Preprints 214601 g007
Figure 8. Confusion matrix of epochs peak Vs. non-peak.
Figure 8. Confusion matrix of epochs peak Vs. non-peak.
Preprints 214601 g008
Table 1. Summary of related work: shaded cells represent no prior work done on the speech decoding using TCRE
Table 1. Summary of related work: shaded cells represent no prior work done on the speech decoding using TCRE
Reference Electrode Type Application Key Finding
Disc TCRE
Hossain et al. [17] Speech Decoding 85.65% (letters)
83.65% (digits)
Liu et al. [18] Speech Decoding 34.7% covert speech
Milyani and Attar [19] Speech Decoding 82.4% (Transformer)
Alharbi and Alotaibi [20] Speech Decoding 75.2%
Abdulghani et al. [21] Speech Decoding 92.50%
Besio et al. [23] Motor Task SNR improved from 7.23 to 30.46
Besio et al. [10] HFO Detection 35.5% onset seizure detection
Toole et al. [24] HFA Localization HFA localized in onset & irritative zone
Liu et al. [25] Spatial Resolution 10× improvement
Alzahrani et al. [26] Motor Task Improved finger movement discrimination
Table 2. All participants’ results using TCRE and disc electrodes.
Table 2. All participants’ results using TCRE and disc electrodes.
TCRE(%) Disc(%)
Participants KNN FCNNN CNN KNN FCNNN CNN
P01 55.0 45.0 45.0 32.5 47.5 50.0
P02 85.0 72.5 75.0 55.0 45.0 77.5
P03 75.0 75.0 75.5 60.0 37.5 68.0
P04 67.5 80.0 67.5 35.0 52.5 65.0
P05 90.0 82.5 87.5 65.0 65.0 82.5
P06 50.0 57.49 52.5 62.5 65.0 60.0
P07 92.5 57.49 92.5 70.0 50.0 85.0
P08 77.5 50.0 87.5 75.0 47.5 85.0
P09 47.5 50.0 40.0 52.5 40.0 65.0
P10 50.0 45.0 50.0 55.0 45.0 45.0
P11 97.5 82.5 85.5 77.5 65.0 88.75
P12 65.0 60.0 65.0 55.0 65.0 55.0
P13 77.5 70.0 70.0 52.5 52.5 52.5
P14 75.0 40.0 92.0 60.0 42.5 50.0
P15 72.5 47.5 80.0 75.0 47.5 90.0
P16 97.5 47.5 90.0 97.5 42.5 57.49
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.
Copyright: This open access article is published under a Creative Commons CC BY 4.0 license, which permit the free download, distribution, and reuse, provided that the author and preprint are cited in any reuse.
Prerpints.org logo

Preprints.org is a free preprint server supported by MDPI in Basel, Switzerland.

Subscribe

Disclaimer

Terms of Use

Privacy Policy

Privacy Settings

© 2026 MDPI (Basel, Switzerland) unless otherwise stated