Discrimination of various poly(propylene) copolymers and prediction of their ethylene content by near-infrared and Raman spectroscopy in combination with chemometric methods

被引:34
作者
Furukawa, T
Watari, M
Siesler, HW
Ozaki, Y
机构
[1] Kwansei Gakuin Univ, Sch Sci, Dept Chem, Nishinomiya, Hyogo 6628501, Japan
[2] Yokogawa Elect Corp, Ind Measurement Div, Musashino, Tokyo 1808750, Japan
[3] Univ Essen Gesamthsch, Dept Phys Chem, D-45117 Essen, Germany
关键词
near infrared spectroscopy; diffuse reflectance spectroscopy; Raman spectroscopy; copolymer; poly(propylene) (PP); polyethylene (PE);
D O I
10.1002/app.11351
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Near-infrared (NIR) diffuse reflectance (DR) spectra and Fourier-transform (FT) Raman spectra were measured for 12 kinds of block and random poly(propylene) (PP) copolymers with different ethylene content in pellets and powder states to propose calibration models that predict the ethylene content in PP and to deepen the understanding of the NIR and Raman spectra of PP. Band assignments were proposed based calculation of the second derivatives of the original spectra, analysis of loadings and regression coefficient plots of principal component analysis (PCA) and principal component regression (PCR) (predicting the ethylene content) models, and comparison of the NIR and Raman spectra of PP with those of linear low-density polyethylene (LLDPE) with short branches. PCR and partial least squares (PLS) regression were applied to the second derivatives of the NIR spectra and the NIR spectra after multiplicative scatter correction (MSC) to develop the calibration models. After MSC treatment, the original spectra yield slightly better results for the standard error of prediction (SEP) than the second derivatives. A plot of regression coefficients for the PCR model shows peaks due to the CH, groups pointing upwards and those arising from the CH, groups pointing downwards, clearly separating the bands due to CH, and CH, groups. For the Raman data, MSC and normalization were applied to the original spectra, and then PCR and PLS regression were carried out to build the models. The PLS regression for the normalized spectra yields the best results for the correlation coefficient and the SEP. Raman bands at 1438,1296, and 1164 cm(-1) play key roles in the prediction of the ethylene content in PP. The NIR chemometric evaluation of the data gave better results than those derived from the Raman spectra and chemometric analysis. Possible reasons for this observation are discussed. (C) 2002 Wiley Periodicals, Inc.
引用
收藏
页码:616 / 625
页数:10
相关论文
共 39 条
[11]  
Hummel D.O., 1974, POLYM SPECTROSCOPY
[12]   Real-time analysis of ethylene vinyl acetate random copolymers using near infrared spectroscopy during extrusion [J].
Khettry, A ;
Hansen, MG .
POLYMER ENGINEERING AND SCIENCE, 1996, 36 (09) :1232-1243
[13]  
KLOPFFER W, 1984, INTRO POLYM SPECTROS, pCH6
[14]   DISPERSIVE AND FOURIER-TRANSFORM NEAR-INFRARED SPECTROSCOPY OF POLYMERIC MATERIALS [J].
LACHENAL, G .
VIBRATIONAL SPECTROSCOPY, 1995, 9 (01) :93-100
[15]   Rapid and nondestructive analysis of the ethylene content of propylene/ethylene copolymer by near-infrared spectroscopy [J].
Lee, JS ;
Chung, H .
VIBRATIONAL SPECTROSCOPY, 1998, 17 (02) :193-201
[16]   COMPARISON OF MID-IR WITH NIR IN POLYMER ANALYSIS [J].
LEE, KAB .
APPLIED SPECTROSCOPY REVIEWS, 1993, 28 (03) :231-284
[17]   VIBRATIONAL-SPECTRUM OF SYNDIOTACTIC POLYPROPYLENE - RAMAN TACTICITY BANDS AND LOCAL STRUCTURES OF ISOTACTIC AND SYNDIOTACTIC POLYPROPYLENES [J].
MASETTI, G ;
CABASSI, F ;
ZERBI, G .
POLYMER, 1980, 21 (02) :143-152
[18]   NEAR-INFRARED SPECTROSCOPY OF SYNTHETIC-POLYMERS [J].
MILLER, CE .
APPLIED SPECTROSCOPY REVIEWS, 1991, 26 (04) :277-339
[19]   PRINCIPLES AND APPLICATIONS OF QUALITY-CONTROL BY NEAR-INFRARED SPECTROSCOPY USING THE EXAMPLE OF POLYMER ADDITIVES [J].
MOLT, K ;
IHLBROCK, D .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1994, 348 (8-9) :523-529
[20]   Determination of two-dimensional correlation spectra using the Hilbert transform [J].
Noda, I .
APPLIED SPECTROSCOPY, 2000, 54 (07) :994-999