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1.
Xin‐Gui Li 《应用聚合物科学杂志》1999,71(11):1887-1892
The thermal degradation and kinetics of poly(2,6‐dimethylphenylene oxide) (PPO) were studied by high‐resolution thermogravimetry. The thermogravimetry measurements were conducted at an initial heating rate of 50°C min−1, resolution 4.0, and sensitivity 1.0 in both nitrogen and air from room temperature to 900°C. A two‐step degradation process was clearly revealed in air at the temperatures of 430°C and 521°C. The thermal degradation temperatures and kinetic parameters of the PPO appear to be higher in air than in nitrogen, indicative of a higher thermostability in air. The temperature, activation energy, order, and frequency factor of the thermal degradation of the PPO in nitrogen are 419°C, 100–120 kJ mol−1, 0.5, and 13–17 min−1, respectively. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 1887–1892, 1999 相似文献
2.
An advanced heat‐resistant fiber (trade name Ekonol) spun from a nematic liquid crystalline melt of thermotropic wholly aromatic poly(p‐oxybenzoate‐p,p′‐biphenylene terephthalate) has been subjected to a dynamic thermogravimetry in nitrogen and air. The thermostability of the Ekonol fiber has been studied in detail. The thermal degradation kinetics have been analyzed using six calculating methods including five single heating rate methods and one multiple heating rate method. The multiple heating‐rate method gives activation energy (E), order (n), frequency factor (Z) for the thermal degradation of 314 kJ mol−1, 4.1, 7.02 × 1020 min−1 in nitrogen, and 290 kJ mol−1, 3.0, 1.29 × 1019 min−1 in air, respectively. According to the five single heating rate methods, the average E, n, and Z values for the degradation were 178 kJ mol−1, 2.1, and 1.25 × 1010 min−1 in nitrogen and 138 kJ mol−1, 1.0, and 6.04 × 107 min−1 in air, respectively. The three kinetic parameters are higher in nitrogen than in air from any of the calculating techniques used. The thermostability of the Ekonol fiber is substantially higher in nitrogen than in air, and the decomposition rate in air is higher because oxidation process is occurring and accelerates thermal degradation. The isothermal weight‐loss results predicted based on the nonisothermal kinetic data are in good agreement with those observed experimentally in the literature. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 1923–1931, 1999 相似文献
3.
Thermotropic liquid‐crystalline copoly(ester‐amide)s consisting of three units of p‐oxybenzoate (B), ethylene terephthalate (E) and p‐benzamide (A) were studied by proton nuclear magnetic resonance at 200 and 400 MHz, wide‐angle X‐ray diffraction, and high‐resolution thermogravimetry to ascertain their molecular and supermolecular structures, thermostability and kinetics parameters of thermal decomposition in both nitrogen and air. The assignments of all resonance peaks of [1H]NMR spectra for the copoly(ester‐amide)s are given and the characteristics of X‐ray equatorial and meridional scans are discussed. Overall activation energy data of the first major decomposition have been evaluated through three calculating techniques. The thermal degradation occurs in three steps in nitrogen and air. The degradation temperatures are higher than 447 °C in nitrogen and 440 °C in air and increase with increasing B‐unit content at a fixed A‐unit content of 5 mol%. The temperatures at the first maximum weight‐loss rate are higher than 455 °C in nitrogen and 445 °C in air and also increase with an increase in B‐unit content. The first maximum weight‐loss rates range between 11.1 and 14.5%min−1 in nitrogen and between 11.9 and 13.5%min−1 in air. The char yields at 500 °C in both nitrogen and air range from 45.8 to 54.3 wt% and increase with increasing B‐unit content. But the char yields at 800 °C in nitrogen and air are quite irregular with the variation of copolymer composition and testing atmosphere. The activation energy and Ln (pre‐exponential factor) for the first major decomposition are usually higher in nitrogen than in air and increase slightly with an increase in B‐unit content at a given A‐unit content of 5 mol%. The activation energy, decomposition order, and Ln (pre‐exponential factor) of the thermal degradation for the copoly(ester‐amide)s in two testing atmospheres, are situated in the ranges of 210–292 kJmol−1, 2.0–2.8, 33–46 min−1, respectively. The three kinetic parameters of the thermal degradation for the aromatic copoly(ester‐amide)s obtained by high‐resolution thermogravimetry at a variable heating rate are almost the same as those by traditional thermogravimetry at constant heating rate, suggesting good applicability of kinetic methods developed for constant heating rate to the variable heating‐rate method. These results indicate that the copoly(ester‐amide)s exhibit high thermostability. The isothermal decomposition kinetics of the copoly(ester‐amide)s at 450 and 420 °C are also discussed and compared with the results obtained based on non‐isothermal high‐resolution thermogravimetry. © 1999 Society of Chemical Industry 相似文献
4.
In this work, 2‐(3‐p‐bromophenyl‐3‐methylcyclobutyl)‐2‐hydroxyethylmethacrylate (BPHEMA) [monomer] was synthesized by the addition of methacrylic acid to 1‐epoxyethyl‐3‐bromophenyl‐3‐methyl cyclobutane. The monomer and poly(BPHEMA) were characterized by FT‐IR and [1H] and [13C]NMR. Average molecular weight, glass transition temperature, solubility parameter, and density of the polymer were also determined. Thermal degradation of poly[BPHEMA] was studied by thermogravimetry (TG), FT‐IR. Programmed heating was carried out at 10 °C min−1 from room temperature to 500 °C. The partially degraded polymer was examined by FT‐IR spectroscopy. The degradation products were identified by using FT‐IR, [1H] and [13C]NMR and GC‐MS techniques. Depolymerization is the main reaction in thermal degradation of the polymer up to about 300 °C. Percentage of the monomer in CRF (Cold Ring Fraction) was estimated at 33% in the peak area of the GC curve. Intramolecular cyclization and cyclic anhydride type structures were observed at temperatures above 300 °C. The liquid products of the degradation, formation of anhydride ring structures and mechanism of degradation are discussed. © 1999 Society of Chemical Industry 相似文献
5.
A novel high‐resolution thermogravimetry (TG) technique in a variable heating rate mode that maximizes resolution and minimizes the time required for TG experiments has been performed for evaluating the thermal degradation and its kinetics of Kevlar fiber in the temperature range ∼ 25–900°C. The degradation of Kevlar in nitrogen or air occurs in one step. The decomposition rate and char yield at 900°C are higher in air than in nitrogen, but the degradation temperature is higher in nitrogen than in air. The initial degradation temperature and maximal degradation rate for Kevlar are 520°C and 8.2%/min in air and 530°C and 3.5%/min in nitrogen. The different techniques for calculating the kinetic parameters are compared. The respective activation energy, order, and natural logarithm of preexponential factor of the degradation of Kevlar are achieved at average values of 133 kJ/mol (or 154 kJ/mol), 0.7 (or 1.1), and 16 min−1 (or 20 min−1) in air (or nitrogen). The technique based on the principle that the maximum weight loss rate is observed at the minimum heating rate gives thermal degradation results that were in excellent agreement with values determined by traditional TG experiments. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 565–571, 1999 相似文献
6.
Xin‐Gui Li 《应用聚合物科学杂志》1999,74(8):2016-2028
Two series of thermotropic liquid crystalline copolyesters containing mainly the p‐oxybenzoate unit were studied by thermogravimetry to ascertain the kinetic parameters of their thermal degradation by six multiple heating‐rate techniques for the first time. The two copolyesters are (1) poly(p‐oxybenzoate‐co‐ethylene terephthalate‐co‐vanillate) and (2) poly(p‐oxybenzoate‐co‐2,6‐oxynaphthoate). The effect of copolymer composition, degradation stage, and test atmosphere on the three kinetic parameters of the thermal degradation in the weight loss range from 5 to 70% is discussed. Comparison of the multiple heating‐rate techniques with single heating‐rate techniques for calculating the kinetic parameters of thermal degradation was made. The respective activation energy, order, and natural logarithm of the frequency factor of the thermal degradation in nitrogen for the poly(p‐oxybenzoate‐co‐ethylene terephthalate‐co‐vanillate)s are between 180 and 230 kJ/mol, between 2.0 and 5.0, and between 28 and 38 min−1 for the first degradation step and between 250 and 390 kJ/mol, between 6.4 and 7.6, and between 38 and 64 min−1 for the second degradation step of the poly(p‐oxybenzoate‐co‐ethylene terephthalate‐co‐vanillate)s with the unit‐B content in the range of 70–75 mol %. The respective activation energy, order, and natural logarithm of frequency factor of the first degradation stage for the poly(p‐oxybenzoate‐co‐2,6‐oxynaphthoate) (Vectra) are between 380 and 570 kJ/mol, between 2.0 and 3.1, and between 55 and 68 min−1 in nitrogen and between 160 and 210 kJ/mol, between 0.8 and 1.8, and between 25 and 32 min−1 in air. The best methods of calculating the kinetic parameters of the thermal degradation for the copolymers are suggested. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 2016–2028, 1999 相似文献
7.
The crystallization process of poly(1‐butene) and its blends with hydrogenated oligocyclopentadiene was analyzed in dependence on composition. Both isothermal and nonisothermal crystallization processes were studied, and the isothermal crystallization process was investigated starting from both the glass and the melt states. Results revealed that spherulite growth rate, overall crystallization rate, and morphology are strongly dependent on crystallization conditions and blend composition. Nonisothermal crystallization data were analyzed according to the theories of Ozawa and Ziabicki. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 1677–1690, 1999 相似文献
8.
A new kind of thermotropic liquid crystalline, poly(oxybenzoate‐co‐trimethylene terephthalate), was prepared from p‐hydroxybenzoic acid (B) and poly(trimethylene terephthalate) (PTT or T) by melting polycondensation. The monomer ratio of B to T is 60:40. The dynamic thermogravimetric kinetics of the copolymer B/T (60:40) and PTT in nitrogen were analyzed by four single heating rate techniques and two multiple heating rate techniques. The effects of the heating rate and the calculating technique on the thermostable and degradation kinetic parameters of the B/T copolymer and PTT are systematically discussed. The four single heating rate techniques used in this work include Friedman, Freeman‐Carroll, Chang, and the second Kissinger techniques, whereas the two multiple heating rate techniques are the first Kissinger and Flynn‐Wall techniques. Additionally, the isothermal thermogravimetric kinetics of B/T (60:40) in nitrogen were investigated by the Flynn technique. The activation energy, the order, and the frequency factor of the degradation reaction for B/T (60:40) copolymer are determined to be 185 kJ/mol, 1.8, and 7.14 × 1013 min−1, respectively. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 2025–2036, 2000 相似文献
9.
8‐Hydroxy‐4‐azoquinolinephenylmethacrylate (8H4AQPMA) was prepared and polymerized in ethyl methyl ketone (EMK) at 65°C using benzoyl peroxide as free radical initiator. Poly(8‐hydroxy‐4‐azoquinolinephenylmethacrylate) poly(8H4AQPMA) was characterized by infrared and nuclear magnetic resonance techniques. The molecular weight of the polymer was determined by gel permeation chromatography. Cu(II) and Ni(II) complexes of poly(8H4AQPMA) were prepared. Elemental analysis of polychelates suggests that the metal‐ligand ratio is about 1 : 2. The polychelates were further characterized by infrared spectra, X‐ray diffraction, spectral studies, and magnetic moments. Thermal analyses of the polymer and polychelates were carried out in air. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 1516–1522, 2006 相似文献
10.
Xin‐Gui Li 《应用聚合物科学杂志》1999,71(4):573-578
Cellulose dinitrate (CDN), cellulose diacetate (CDA), and cellulose triacetate (CTA) were subjected to high‐resolution thermogravimetry (TG) at a variable heating rate in air. The TG curves, the derivative TG curves, the second derivative TG curves, and heating rate curves are discussed. The thermal degradation temperature and kinetic parameters are presented and compared to those obtained with traditional TG at a constant heating rate. The degradation process of the cellulose esters is speculated. Among the three cellulose esters, CDN exhibits the lowest degradation temperature of (213°C) but the largest degradation activation energy of (237–269 kJ/mol). © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 573–578, 1999 相似文献
11.
Qiang Zhang Youquan Zhang Dewan Xia Yun Zhao Yanqiao Shi Qingze Jiao 《应用聚合物科学杂志》2009,112(3):1271-1277
Poly(4‐methyl‐1‐pentene) was used to prepare porous structures by a thermally induced phase‐separation method. Different porous structures were obtained with poly(4‐methyl‐1‐pentene), which has excellent properties as a polymer, and diphenyl ether as a diluent. The affecting factors, including the polymer concentration and cooling temperature, are discussed. Scanning electron microscopy images and porosity values were obtained to investigate the affecting factors. According to the cloud‐point temperature and crystallization temperature, a phase diagram was also obtained to explain the phase‐separation process. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 相似文献
12.
Poly(trimethylene terephthalate) was investigated by isothermal thermogravimetry in nitrogen at six temperatures, including 304, 309, 314, 319, 324, and 336°C. The isothermal data have been analyzed using both a peak maximum technique and an iso‐conversional procedure. Both techniques gave apparent activation energies of 201 and 192 kJ mol?1, respectively, for the isothermal degradation of poly(trimethylene terephthalate) in nitrogen. The decomposition reaction order is calculated to be 1.0. The natural logarithms of the frequency factor based on the peak maximum and the iso‐conversional techniques are 36 and 34 min?1, respectively, for poly(trimethylene terephthalate) decomposed isothermally in nitrogen. These isothermal kinetic parameters are in good agreement with those derived by the Kissinger technique on the basis of the dynamic thermogravimetric data reported elsewhere (209 kJ mol?1, 1.0 and 37 min?1). The isothermal decomposition of poly(trimethylene terephthalate) in nitrogen undergoes two processes, a relative fast degradation process in the initial period and a subsequent one with a slower weight‐loss rate. The former process may be due to the removal of ester groups, trimethylene groups, and aromatic hydrogen atoms from the chain of poly(trimethylene terethphalate). The latter one may be ascribed to the further pyrolysis of the carbonaceous char. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 1600–1608, 2002; DOI 10.1002/app.10476 相似文献
13.
The kinetics of thermal degradation of thermotropic liquid crystalline poly(p‐oxybenzoate‐co‐ethylene‐2,6‐naphthalate) (PHB/PEN) with the monomer ratio of 60 : 40 and PEN in nitrogen was studied by dynamic thermogravimetry (TG). The kinetic parameters, including the activation energy Ea, the reaction order n, and the frequency factor ln(Z) of the degradation reaction for PHB/PEN (60 : 40) and PEN were analyzed by the single heating rate methods of Friedman and Chang. The effects of the heating rate and the calculating method on the thermostable and degradation kinetic parameters are systematically discussed. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91:3915–3920, 2004 相似文献
14.
A series of new aromatic poly(amide‐imide)s were synthesized by the triphenyl phosphite‐activated polycondensation of the diimide‐diacid, 1,4‐bis(trimellitimido)‐2,5‐dichlorobenzene (I), with various aromatic diamines in a medium consisting of N‐methyl‐2‐pyrrolidone (NMP), pyridine, and calcium chloride. The poly(amide‐imide)s had inherent viscosities of 0.88–1.27 dL g−1. The diimide‐diacid monomer (I) was prepared from 2,5‐dichloro‐p‐phenylenediamine with trimellitic anhydride. All the resulting polymers were amorphous and were readily soluble in a variety of organic solvents, including NMP and N,N‐dimethylacetamide. Transparent, flexible, and tough films of these polymers could be cast from N,N‐dimethylacetamide or NMP solutions. Cast films had tensile strengths ranging from 92 to 127 MPa, elongations at break from 4 to 24%, and initial moduli from 2.59 to 3.65 GPa. The glass transition temperatures of these polymers were in the range of 256°–317°C, and the 10% weight loss temperatures were above 430°C in nitrogen. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 73: 271–278, 1999 相似文献
15.
A novel bismaleimide, 2,2′‐dimethyl‐4,4′‐bis(4‐maleimidophenoxy)biphenyl, containing noncoplanar 2,2′‐dimethylbiphenylene and flexible ether units in the polymer backbone was synthesized from 2,2′‐dimethyl‐4,4′‐bis(4‐aminophenoxy)biphenyl with maleic anhydride. The bismaleimide was reacted with 11 diamines using m‐cresol as a solvent and glacial acetic acid as a catalyst to produce novel polyaspartimides. Polymers were identified by elemental analysis and infrared spectroscopy, and characterized by solubility test, X‐ray diffraction, and thermal analysis (differential scanning calorimetry and thermogravimetric analysis). The inherent viscosities of the polymers varied from 0.22 to 0.48 dL g−1 in concentration of 1.0 g dL−1 of N,N‐dimethylformamide. All polymers are soluble in N‐methyl‐2‐pyrrolidone, N,N‐dimethylacetamide, N,N‐dimethylformamide, dimethylsulfoxide, pyridine, m‐cresol, and tetrahydrofuran. The polymers, except PASI‐4, had moderate glass transition temperature in the range of 188°–226°C and good thermo‐oxidative stability, losing 10% mass in the range of 375°–426°C in air and 357°–415°C in nitrogen. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 73: 279–286, 1999 相似文献
16.
The thermal degradation kinetics of poly(3‐hydroxybutyrate) (PHB) and poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) [poly(HB–HV)] under nitrogen was studied by thermogravimetry (TG). The results show that the thermal degradation temperatures (To, Tp, and Tf) increased with an increasing heating rate (B). Poly(HB–HV) was thermally more stable than PHB because its thermal degradation temperatures, To(0), Tp(0), and Tf(0)—determined by extrapolation to B = 0°C/min—increased by 13°C–15°C over those of PHB. The thermal degradation mechanism of PHB and poly(HB–HV) under nitrogen were investigated with TG–FTIR and Py–GC/MS. The results show that the degradation products of PHB are mainly propene, 2‐butenoic acid, propenyl‐2‐butenoate and butyric‐2‐butenoate; whereas, those of poly(HB–HV) are mainly propene, 2‐butenoic acid, 2‐pentenoic acid, propenyl‐2‐butenoate, propenyl‐2‐pentenoate, butyric‐2‐butenoate, pentanoic‐2‐pentenoate, and CO2. The degradation is probably initiated from the chain scission of the ester linkage. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 1530–1536, 2003 相似文献
17.
[2,6‐Bis(4‐hydroxybenzylidene)cyclohexanone] (HBC) was prepared by reacting cyclohexanone and p‐hydroxybenzaldehyde in the presence of acid catalyst. Acrylated derivative of HBC, 4‐{[‐3‐(4‐hydroxybenzylidene)‐2‐oxocyclohexylidene]methyl}phenyl acrylate (HBA), was prepared by reacting HBC with acryloyl chloride in the presence of triethylamine. Copolymers of HBA with styrene (S) and methyl acrylate (MA) of different feed compositions were carried out by solution polymerization technique by using benzoyl peroxide (BPO) under nitrogen atmosphere. All monomers and polymers were characterized by using IR and NMR techniques. Reactivity ratios of the monomers present in the polymer chain were evolved by using Finnman–Ross (FR), Kelen–Tudos (KT), and extended Kelen–Tudos (ex‐KT) methods. Average values of reactivity were achieved by the following three methods: r1 (S) = 2.36 ± 0.45 and r2 (HBA) = 0.8 ± 0.31 for poly(S‐co‐HBA); r1 = 1.62 ± 0.06 (MA); and r2 = 0.12 ± 0.07 (HBA) for poly(MA‐co‐HBA). The photocrosslinking property of the polymers was done by using UV absorption spectroscopic technique. The rate of photocrosslinking was enhanced compared to that of the homopolymers, when the HBA was copolymerized with S and MA. Thermal stability and molecular weights (Mw and Mn) were determined for the polymer samples. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 2494–2503, 2004 相似文献
18.
An imide ring‐performed dicarboxylic acid bearing one hexafluoroisopropylidene and two ether linkages between aromatic rings, 2,2‐bis[4‐(4‐trimellitimidophenoxy)phenyl]hexafluoropropane (II), was prepared from the condensation of 2,2‐bis[4‐(4‐aminophenoxy)phenyl]hexafluoropropane and trimellitic anhydride. A novel series of poly(amide‐imide)s having inherent viscosities of 0.72 ∼ 1.86 dL g−1 was prepared by the triphenyl phosphite‐activated polycondensation from the diimide‐diacid (II) with various aromatic diamines in a medium consisting of N‐methyl‐2‐pyrolidone, pyridine, and calcium chloride. Several of the resulting polymers were soluble in polar amide solvents, and their solutions could be cast into transparent, thin, flexible films having good tensile properties and high thermal stability. The 10% weight loss temperatures were all above 495°C in air or nitrogen atmosphere, and the glass transition temperatures were in the range of 237°–276°C. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 823–831, 1999 相似文献
19.
The degradation of poly(aryl ether ketone) containing 2,7‐naphthalene moieties was subjected to dynamic and isothermal thermogravimetry in nitrogen and air. The dynamic experiments showed that the initial degradation temperature, temperature for 5% weight loss, and temperature corresponding to the maximum degradation rate of poly(aryl ether ketone) containing 2,7‐naphthalene moieties were a little higher than those of poly(ether ether ketone) and almost independent of the 2,7‐naphthalene moiety content. The thermal stability of poly(aryl ether ketone) containing 2,7‐naphthalene moieties in air was substantially less than that in nitrogen, and the degradation mechanism was more complex. The results obtained under the isothermal conditions were in agreement with the corresponding results obtained in nitrogen and air under the dynamic conditions. In the dynamic experiments, the apparent activation energies for the degradation processes were 240 and 218 kJ/mol in nitrogen and air for the second reaction stage as the heating rate was higher than 5°C/min. In the isothermal experiments, the apparent activation energies for the degradation processes were 222 and 190 kJ/mol in nitrogen and air, respectively. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
20.
Thermotropic liquid crystalline terpolymers consisting of three units of p-oxybenzoate (B), ethylene terephthalate (E), and m-oxybenzoate (M), were investigated through high-resolution thermogravimetry to evaluate their stability and kinetic parameters of thermal degradation in nitrogen and air. Overall activation energy data of the first major decomposition was calculated through three calculating methods. Thermal degradation occurs in three major steps in both nitrogen and air. Three kinds of degradation temperatures (Td, Tm1, Tm2) are slightly higher and the first maximum weight-loss rates are slightly lower in nitrogen than in air, suggesting a higher thermostability in nitrogen. The thermal degradation temperatures range from 450 to 457°C in nitrogen and 441 to 447°C in air and increase with increasing B-unit content at a fixed M-unit content of 5 mol %. The temperatures at the first maximum weight loss rate range from 452 to 466°C in nitrogen and 444 to 449°C in air and increase slightly with an increase in B-unit content. The first and second maximum weight-loss rates are maintained at almost 9.2–10.8 and 4.0–6.1%/min in nitrogen (11.2–12.0 and 3.9–4.2%/min in air) and vary slightly with copolymer composition. The residues after the first major step of degradation are predicted on the basis of the complete exclusion of ester and ethylene groups and hydrogen atoms and compared with those observed experimentally. The char yields at 500°C in both nitrogen and air are larger than 42.6 wt % and increase with increasing B-unit content. However, the char yields at 800°C in nitrogen and air are different. The activation energy and ln(pre-exponential factor) for the first major decomposition are slightly higher in nitrogen than in air and increase with an increase in B-unit content at a given M-unit content of 5 mol %. There is no regular variation in the decomposition order with the variation of copolymer composition and testing atmosphere. The activation energy, decomposition order, and ln(pre-exponential factor) of the thermal degradation for the terpolymers are located in the ranges of 212–263 kJ mol−1, 2.4–3.5, 33–41 min−1, respectively. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 73: 2911–2919, 1999 相似文献