Gel time prediction of multifunctional acrylates using a kinetics model

被引:26
作者
Boddapati, Aparna [1 ]
Rahane, Santosh B. [1 ]
Slopek, Ryan P. [1 ]
Breedveld, Victor [1 ]
Henderson, Clifford L. [1 ]
Grover, Martha A. [1 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biomol Engn, Atlanta, GA 30332 USA
关键词
Photopolymerization; Gel time; Microrheology; FREE-RADICAL POLYMERIZATION; MULTI(METH)ACRYLATE MONOMERS; METHYL-METHACRYLATE; REACTION-DIFFUSION; PHOTOPOLYMERIZATION; STEREOLITHOGRAPHY; SIMULATION; CONSTANTS; GELATION; OXYGEN;
D O I
10.1016/j.polymer.2010.12.024
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A kinetics model for prediction of double-bond conversion and gel time in the photopolymerization of multifunctional acrylates is presented. The system consisting of a trifunctional acrylate, trimethylolpropane triacrylate (TMPTA), and a photoinitiator, 2,2-dimethoxy-1,2-diphenylethan-1-one (DMPA), was studied using Fourier-transform infrared spectroscopy (FTIR) measurements to monitor double-bond conversion and microrheology techniques to quantify the gel time for this system. Rate constants for the kinetics model were first estimated by fitting the model only to the FTIR double-bond conversion data, and later to both the FTIR and microrheology data. The measured gel time correlated with both the calculated initial rate of radical generation and a constant value of the predicted double-bond conversion, over a broad range of conditions. The model allows for materials formulation and exposure source intensity variables to be included in stereolithography inverse problem solutions, and could be applied to other cross-linking based photopolymerization systems. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:866 / 873
页数:8
相关论文
共 27 条
[1]   KINETIC EVIDENCE OF REACTION-DIFFUSION DURING THE POLYMERIZATION OF MULTI(METH)ACRYLATE MONOMERS [J].
ANSETH, KS ;
WANG, CM ;
BOWMAN, CN .
MACROMOLECULES, 1994, 27 (03) :650-655
[2]   REACTION BEHAVIOR AND KINETIC CONSTANTS FOR PHOTOPOLYMERIZATIONS OF MULTI(METH)ACRYLATE MONOMERS [J].
ANSETH, KS ;
WANG, CM ;
BOWMAN, CN .
POLYMER, 1994, 35 (15) :3243-3250
[3]   Coupling chain length dependent and reaction diffusion controlled termination in the free radical polymerization of multivinyl (meth)acrylates [J].
Berchtold, KA ;
Lovestead, TM ;
Bowman, CN .
MACROMOLECULES, 2002, 35 (21) :7968-7975
[4]   A KINETIC GELATION METHOD FOR THE SIMULATION OF FREE-RADICAL POLYMERIZATIONS [J].
BOWMAN, CN ;
PEPPAS, NA .
CHEMICAL ENGINEERING SCIENCE, 1992, 47 (06) :1411-1419
[5]   KINETIC APPROACH OF O-2 INHIBITION IN ULTRAVIOLET-INDUCED AND LASER-INDUCED POLYMERIZATIONS [J].
DECKER, C ;
JENKINS, AD .
MACROMOLECULES, 1985, 18 (06) :1241-1244
[6]   A PROCESS MODEL FOR NONISOTHERMAL PHOTOPOLYMERIZATION WITH A LASER-LIGHT SOURCE .1. BASIC MODEL DEVELOPMENT [J].
FLACH, L ;
CHARTOFF, RP .
POLYMER ENGINEERING AND SCIENCE, 1995, 35 (06) :483-492
[7]   Molecular size distribution in three dimensional polymers. I. Gelation [J].
Flory, PJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1941, 63 :3083-3090
[8]   LASER INVESTIGATION OF NORRISH TYPE-I PHOTOSCISSION IN THE PHOTOINITIATOR IRGACURE (2,2-DIMETHOXY 2-PHENYL-ACETOPHENONE) [J].
FOUASSIER, JP ;
MERLIN, A .
JOURNAL OF PHOTOCHEMISTRY, 1980, 12 (01) :17-23
[9]   Development of a comprehensive free radical photopolymerization model incorporating heat and mass transfer effects in thick films [J].
Goodner, MD ;
Bowman, CN .
CHEMICAL ENGINEERING SCIENCE, 2002, 57 (05) :887-900
[10]  
GOODNER MD, 1998, NAT M AM CHEM SOC, V713, P220