An insight into the sequential order in 2D correlation spectroscopy using polymer transitions: Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative, and Asymmetric Sigmoid. Findings in experiments and simulations

In this paper, we found the curves of infrared spectral intensity at specific wavenumbers of several polymer transitions can be accurately fitted by one of Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative, or Asymmetric Sigmoid functions. These transitions include the melting of iPP, the B...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Vibrational spectroscopy 2014-01, Vol.70, p.137-161
Hauptverfasser: Zhou, Tao, Peng, Leilei, Liu, Yongcheng, Zhan, Yanhui, Liu, Feiwei, Zhang, Aiming
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 161
container_issue
container_start_page 137
container_title Vibrational spectroscopy
container_volume 70
creator Zhou, Tao
Peng, Leilei
Liu, Yongcheng
Zhan, Yanhui
Liu, Feiwei
Zhang, Aiming
description In this paper, we found the curves of infrared spectral intensity at specific wavenumbers of several polymer transitions can be accurately fitted by one of Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative, or Asymmetric Sigmoid functions. These transitions include the melting of iPP, the Brill transition of PA66, the epoxy curing, the oxidation of SBS, and the melting of HDPE. These functions were obviously different from other important functions, which were earlier introduced into generalized 2D correlation spectroscopy, such as sinusoidal, exponential, and Lorentzian. The properties of the Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative functions were studied using the simulated infrared spectra. The sequential order is only controlled by the parameter reflecting the center point location, while other parameter values have no relationship. The influences of the parameters in Asymmetric Sigmoid on the sequential order were also studied using the simulated IR spectra. Within the transition range, it was found the values of several waveform parameters co-determine the sequential order. We concluded that the MW2D or PCMW2D method should first be employed to determine a rational transition range before using 2D correlation infrared spectroscopy to study the mechanism of the polymer transitions. The clear physical meaning of the sequential order is the “earlier” or “later” of the transition points. As long as the experimental range (external perturbation) is wide enough and the data precision is good, the sequential order is absolutely reliable within the transition range. The results discussed throughout this paper have proven that the sequential order rules are absolutely correct. The content of the present study will solve the controversy on the sequential order rules to a large extent.
doi_str_mv 10.1016/j.vibspec.2013.12.001
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1677963361</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0924203113001586</els_id><sourcerecordid>1551039241</sourcerecordid><originalsourceid>FETCH-LOGICAL-c408t-efdebd4d1f91070833aa4a9b279b95bcbaebf122ebf44cf1f9450626f44493533</originalsourceid><addsrcrecordid>eNqNUsuO0zAUtRBIlMInIHnJYhL8yKNhg0phBqRKLIC15Tg3HVeJHWynms6n8jXc0GHBatjYsn0e1j2HkNec5Zzx6u0xP9k2TmBywbjMucgZ40_Iim9qmcmqqZ-SFWtEkQkm-XPyIsYjY6wquVyRX1tHrYv2cJtwT56mW6ARfs7gktUD9aGDgC9UfKTGhwCDTtY7util4KPx05nO0boDnfxwHhGcgkbBBRXf0Q9-SPejdo5-s4fR2-6K3ug5Rqsd3c3jvMid4IrufUDH-3_utOvoNp7HEVKw5q9ATq-t69AwLt-CuwmCHZEb_-CjvfDR_CV51ushwquHfU1-XH_6vvuc7b_efNlt95kp2CZl0HfQdkXH-4azmm2k1LrQTSvqpm3K1rQa2p4LgWtRmB5hRckqUeGpaGQp5Zq8uehOwePcYlKjjQaGQTvwc1S8quumkrLij0PLkjOJUf0PVLJmIxlmvCblBWowkBigVxOORIez4kwtDVFH9dAQtTREcaGwIch7f-EBTudkIahoLDgDnQ2Yruq8fUThN6XjzUQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1530983087</pqid></control><display><type>article</type><title>An insight into the sequential order in 2D correlation spectroscopy using polymer transitions: Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative, and Asymmetric Sigmoid. Findings in experiments and simulations</title><source>Elsevier ScienceDirect Journals</source><creator>Zhou, Tao ; Peng, Leilei ; Liu, Yongcheng ; Zhan, Yanhui ; Liu, Feiwei ; Zhang, Aiming</creator><creatorcontrib>Zhou, Tao ; Peng, Leilei ; Liu, Yongcheng ; Zhan, Yanhui ; Liu, Feiwei ; Zhang, Aiming</creatorcontrib><description>In this paper, we found the curves of infrared spectral intensity at specific wavenumbers of several polymer transitions can be accurately fitted by one of Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative, or Asymmetric Sigmoid functions. These transitions include the melting of iPP, the Brill transition of PA66, the epoxy curing, the oxidation of SBS, and the melting of HDPE. These functions were obviously different from other important functions, which were earlier introduced into generalized 2D correlation spectroscopy, such as sinusoidal, exponential, and Lorentzian. The properties of the Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative functions were studied using the simulated infrared spectra. The sequential order is only controlled by the parameter reflecting the center point location, while other parameter values have no relationship. The influences of the parameters in Asymmetric Sigmoid on the sequential order were also studied using the simulated IR spectra. Within the transition range, it was found the values of several waveform parameters co-determine the sequential order. We concluded that the MW2D or PCMW2D method should first be employed to determine a rational transition range before using 2D correlation infrared spectroscopy to study the mechanism of the polymer transitions. The clear physical meaning of the sequential order is the “earlier” or “later” of the transition points. As long as the experimental range (external perturbation) is wide enough and the data precision is good, the sequential order is absolutely reliable within the transition range. The results discussed throughout this paper have proven that the sequential order rules are absolutely correct. The content of the present study will solve the controversy on the sequential order rules to a large extent.</description><identifier>ISSN: 0924-2031</identifier><identifier>EISSN: 1873-3697</identifier><identifier>DOI: 10.1016/j.vibspec.2013.12.001</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Asymmetric Sigmoid ; Asymmetry ; Boltzmann Sigmoid ; Correlation ; Gaussian ; Gaussian Cumulative ; Lorentz Cumulative ; Melting ; Polymer transition ; Sequential order ; Simulation ; Spectra ; Spectroscopy ; Two dimensional ; Two-dimensional correlation infrared spectroscopy ; Waveform</subject><ispartof>Vibrational spectroscopy, 2014-01, Vol.70, p.137-161</ispartof><rights>2013 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-efdebd4d1f91070833aa4a9b279b95bcbaebf122ebf44cf1f9450626f44493533</citedby><cites>FETCH-LOGICAL-c408t-efdebd4d1f91070833aa4a9b279b95bcbaebf122ebf44cf1f9450626f44493533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.vibspec.2013.12.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids></links><search><creatorcontrib>Zhou, Tao</creatorcontrib><creatorcontrib>Peng, Leilei</creatorcontrib><creatorcontrib>Liu, Yongcheng</creatorcontrib><creatorcontrib>Zhan, Yanhui</creatorcontrib><creatorcontrib>Liu, Feiwei</creatorcontrib><creatorcontrib>Zhang, Aiming</creatorcontrib><title>An insight into the sequential order in 2D correlation spectroscopy using polymer transitions: Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative, and Asymmetric Sigmoid. Findings in experiments and simulations</title><title>Vibrational spectroscopy</title><description>In this paper, we found the curves of infrared spectral intensity at specific wavenumbers of several polymer transitions can be accurately fitted by one of Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative, or Asymmetric Sigmoid functions. These transitions include the melting of iPP, the Brill transition of PA66, the epoxy curing, the oxidation of SBS, and the melting of HDPE. These functions were obviously different from other important functions, which were earlier introduced into generalized 2D correlation spectroscopy, such as sinusoidal, exponential, and Lorentzian. The properties of the Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative functions were studied using the simulated infrared spectra. The sequential order is only controlled by the parameter reflecting the center point location, while other parameter values have no relationship. The influences of the parameters in Asymmetric Sigmoid on the sequential order were also studied using the simulated IR spectra. Within the transition range, it was found the values of several waveform parameters co-determine the sequential order. We concluded that the MW2D or PCMW2D method should first be employed to determine a rational transition range before using 2D correlation infrared spectroscopy to study the mechanism of the polymer transitions. The clear physical meaning of the sequential order is the “earlier” or “later” of the transition points. As long as the experimental range (external perturbation) is wide enough and the data precision is good, the sequential order is absolutely reliable within the transition range. The results discussed throughout this paper have proven that the sequential order rules are absolutely correct. The content of the present study will solve the controversy on the sequential order rules to a large extent.</description><subject>Asymmetric Sigmoid</subject><subject>Asymmetry</subject><subject>Boltzmann Sigmoid</subject><subject>Correlation</subject><subject>Gaussian</subject><subject>Gaussian Cumulative</subject><subject>Lorentz Cumulative</subject><subject>Melting</subject><subject>Polymer transition</subject><subject>Sequential order</subject><subject>Simulation</subject><subject>Spectra</subject><subject>Spectroscopy</subject><subject>Two dimensional</subject><subject>Two-dimensional correlation infrared spectroscopy</subject><subject>Waveform</subject><issn>0924-2031</issn><issn>1873-3697</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNUsuO0zAUtRBIlMInIHnJYhL8yKNhg0phBqRKLIC15Tg3HVeJHWynms6n8jXc0GHBatjYsn0e1j2HkNec5Zzx6u0xP9k2TmBywbjMucgZ40_Iim9qmcmqqZ-SFWtEkQkm-XPyIsYjY6wquVyRX1tHrYv2cJtwT56mW6ARfs7gktUD9aGDgC9UfKTGhwCDTtY7util4KPx05nO0boDnfxwHhGcgkbBBRXf0Q9-SPejdo5-s4fR2-6K3ug5Rqsd3c3jvMid4IrufUDH-3_utOvoNp7HEVKw5q9ATq-t69AwLt-CuwmCHZEb_-CjvfDR_CV51ushwquHfU1-XH_6vvuc7b_efNlt95kp2CZl0HfQdkXH-4azmm2k1LrQTSvqpm3K1rQa2p4LgWtRmB5hRckqUeGpaGQp5Zq8uehOwePcYlKjjQaGQTvwc1S8quumkrLij0PLkjOJUf0PVLJmIxlmvCblBWowkBigVxOORIez4kwtDVFH9dAQtTREcaGwIch7f-EBTudkIahoLDgDnQ2Yruq8fUThN6XjzUQ</recordid><startdate>201401</startdate><enddate>201401</enddate><creator>Zhou, Tao</creator><creator>Peng, Leilei</creator><creator>Liu, Yongcheng</creator><creator>Zhan, Yanhui</creator><creator>Liu, Feiwei</creator><creator>Zhang, Aiming</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>201401</creationdate><title>An insight into the sequential order in 2D correlation spectroscopy using polymer transitions: Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative, and Asymmetric Sigmoid. Findings in experiments and simulations</title><author>Zhou, Tao ; Peng, Leilei ; Liu, Yongcheng ; Zhan, Yanhui ; Liu, Feiwei ; Zhang, Aiming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-efdebd4d1f91070833aa4a9b279b95bcbaebf122ebf44cf1f9450626f44493533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Asymmetric Sigmoid</topic><topic>Asymmetry</topic><topic>Boltzmann Sigmoid</topic><topic>Correlation</topic><topic>Gaussian</topic><topic>Gaussian Cumulative</topic><topic>Lorentz Cumulative</topic><topic>Melting</topic><topic>Polymer transition</topic><topic>Sequential order</topic><topic>Simulation</topic><topic>Spectra</topic><topic>Spectroscopy</topic><topic>Two dimensional</topic><topic>Two-dimensional correlation infrared spectroscopy</topic><topic>Waveform</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Tao</creatorcontrib><creatorcontrib>Peng, Leilei</creatorcontrib><creatorcontrib>Liu, Yongcheng</creatorcontrib><creatorcontrib>Zhan, Yanhui</creatorcontrib><creatorcontrib>Liu, Feiwei</creatorcontrib><creatorcontrib>Zhang, Aiming</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Vibrational spectroscopy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Tao</au><au>Peng, Leilei</au><au>Liu, Yongcheng</au><au>Zhan, Yanhui</au><au>Liu, Feiwei</au><au>Zhang, Aiming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An insight into the sequential order in 2D correlation spectroscopy using polymer transitions: Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative, and Asymmetric Sigmoid. Findings in experiments and simulations</atitle><jtitle>Vibrational spectroscopy</jtitle><date>2014-01</date><risdate>2014</risdate><volume>70</volume><spage>137</spage><epage>161</epage><pages>137-161</pages><issn>0924-2031</issn><eissn>1873-3697</eissn><abstract>In this paper, we found the curves of infrared spectral intensity at specific wavenumbers of several polymer transitions can be accurately fitted by one of Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative, or Asymmetric Sigmoid functions. These transitions include the melting of iPP, the Brill transition of PA66, the epoxy curing, the oxidation of SBS, and the melting of HDPE. These functions were obviously different from other important functions, which were earlier introduced into generalized 2D correlation spectroscopy, such as sinusoidal, exponential, and Lorentzian. The properties of the Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative functions were studied using the simulated infrared spectra. The sequential order is only controlled by the parameter reflecting the center point location, while other parameter values have no relationship. The influences of the parameters in Asymmetric Sigmoid on the sequential order were also studied using the simulated IR spectra. Within the transition range, it was found the values of several waveform parameters co-determine the sequential order. We concluded that the MW2D or PCMW2D method should first be employed to determine a rational transition range before using 2D correlation infrared spectroscopy to study the mechanism of the polymer transitions. The clear physical meaning of the sequential order is the “earlier” or “later” of the transition points. As long as the experimental range (external perturbation) is wide enough and the data precision is good, the sequential order is absolutely reliable within the transition range. The results discussed throughout this paper have proven that the sequential order rules are absolutely correct. The content of the present study will solve the controversy on the sequential order rules to a large extent.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.vibspec.2013.12.001</doi><tpages>25</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0924-2031
ispartof Vibrational spectroscopy, 2014-01, Vol.70, p.137-161
issn 0924-2031
1873-3697
language eng
recordid cdi_proquest_miscellaneous_1677963361
source Elsevier ScienceDirect Journals
subjects Asymmetric Sigmoid
Asymmetry
Boltzmann Sigmoid
Correlation
Gaussian
Gaussian Cumulative
Lorentz Cumulative
Melting
Polymer transition
Sequential order
Simulation
Spectra
Spectroscopy
Two dimensional
Two-dimensional correlation infrared spectroscopy
Waveform
title An insight into the sequential order in 2D correlation spectroscopy using polymer transitions: Boltzmann Sigmoid, Gaussian Cumulative, Lorentz Cumulative, and Asymmetric Sigmoid. Findings in experiments and simulations
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T04%3A59%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=An%20insight%20into%20the%20sequential%20order%20in%202D%20correlation%20spectroscopy%20using%20polymer%20transitions:%20Boltzmann%20Sigmoid,%20Gaussian%20Cumulative,%20Lorentz%20Cumulative,%20and%20Asymmetric%20Sigmoid.%20Findings%20in%20experiments%20and%20simulations&rft.jtitle=Vibrational%20spectroscopy&rft.au=Zhou,%20Tao&rft.date=2014-01&rft.volume=70&rft.spage=137&rft.epage=161&rft.pages=137-161&rft.issn=0924-2031&rft.eissn=1873-3697&rft_id=info:doi/10.1016/j.vibspec.2013.12.001&rft_dat=%3Cproquest_cross%3E1551039241%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1530983087&rft_id=info:pmid/&rft_els_id=S0924203113001586&rfr_iscdi=true