Residual alignment and its effect on weld strength in material-extrusion 3D-printing of polylactic acid

被引:61
作者
Costanzo, Andrea [1 ]
Spotorno, Roberto [1 ]
Candal, Maria Virginia [2 ,3 ]
Fernandez, Maria Mercedes [2 ]
Muller, Alejandro J. [2 ,4 ]
Graham, Richard S. [5 ]
Cavallo, Dario [1 ]
McIlroy, Claire [6 ]
机构
[1] Univ Genoa, Dept Chem & Ind Chem, Via Dodecaneso 31, I-16146 Genoa, Italy
[2] Univ Basque Country UPV EHU, POLYMAT & Polymer Sci & Technol Dept, Fac Chem, Paseo Manuel de Lardizabal 3, Donostia San Sebastian 20018, Spain
[3] Univ Simon Bolivar, Dept Mecan, Grp Polimeros, Apartado 89000, Caracas 1080, Venezuela
[4] Basque Fdn Sci, IKERBASQUE, Bilbao, Spain
[5] Univ Nottingham, Sch Math Sci, Nottingham NG7 2RD, England
[6] Univ Lincoln, Sch Math & Phys, Lincoln LN6 7TS, England
基金
英国工程与自然科学研究理事会;
关键词
Material extrusion; Birefringence; Molecular orientation; Weld strength; Polylactic acid; FUSED-FILAMENT-FABRICATION; POLY(LACTIC ACID); POLYMER MELTS; BEHAVIOR; ENTANGLEMENT; ORIENTATION; TOUGHNESS; DYNAMICS;
D O I
10.1016/j.addma.2020.101415
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Gaining a molecular understanding of material extrusion (MatEx) 3D printing is crucial to predicting and controlling part properties. Here we report the direct observation of distinct birefringence localised to the weld regions between the printed filaments, indicating the presence of molecular orientation that is absent from the bulk of the filament. The value of birefringence at the weld increases at higher prints speeds and lower nozzle temperatures, and is found to be detrimental to the weld strength measured by tensile testing perpendicular to the print direction. We employ a molecularly-aware non-isothermal model of the MatEx flow and cooling process to predict the degree of alignment trapped in the weld at the glass transition. We find that the predicted residual alignment factor, (A) over bar, is linearly related to the extent of birefringence, Delta n. Thus, by combining experiments and molecular modelling, we show that weld strength is not limited by inter-diffusion, as commonly expected, but instead by the configuration of the entangled polymer network. We adapt the classic molecular interpretation of glassy polymer fracture to explain how the measured weld strength decreases with increasing print speed and decreasing nozzle temperature.
引用
收藏
页数:13
相关论文
共 39 条
[1]   3D-printing technologies for electrochemical applications [J].
Ambrosi, Adriano ;
Pumera, Martin .
CHEMICAL SOCIETY REVIEWS, 2016, 45 (10) :2740-2755
[2]  
[Anonymous], 2011, POLYLACTIC ACID SYNT
[3]   Flow Effects on Melt Structure and Entanglement Network of Linear Polymers: Results from a Nonequilibrium Molecular Dynamics Simulation Study of a Polyethylene Melt in Steady Shear [J].
Baig, Chunggi ;
Mavrantzas, Vlasis G. ;
Kroger, Martin .
MACROMOLECULES, 2010, 43 (16) :6886-6902
[4]   FRACTURE SURFACE WORK MEASUREMENTS ON GLASSY POLYMERS BY A CLEAVAGE TECHNIQUE .2. EFFECTS OF CROSSLINKING AND PREORIENTATION [J].
BROUTMAN, LJ ;
MCGARRY, FJ .
JOURNAL OF APPLIED POLYMER SCIENCE, 1965, 9 (02) :609-&
[5]   A MOLECULAR INTERPRETATION OF THE TOUGHNESS OF GLASSY-POLYMERS [J].
BROWN, HR .
MACROMOLECULES, 1991, 24 (10) :2752-2756
[6]   Experimental characterization and analytical modelling of the mechanical behaviour of fused deposition processed parts made of ABS-M30 [J].
Croccolo, Dario ;
De Agostinis, Massimiliano ;
Olmi, Giorgio .
COMPUTATIONAL MATERIALS SCIENCE, 2013, 79 :506-518
[7]   EFFECT OF PRE-ORIENTATION ON FRACTURE PROPERTIES OF GLASSY POLYMERS [J].
CURTIS, JW .
JOURNAL OF PHYSICS D-APPLIED PHYSICS, 1970, 3 (10) :1413-&
[8]  
Doi M., 1988, International series of monographs on physics
[9]   Melt rheology of poly(lactic acid): Entanglement and chain architecture effects [J].
Dorgan, JR ;
Williams, JS ;
Lewis, DN .
JOURNAL OF RHEOLOGY, 1999, 43 (05) :1141-1155
[10]   Tearing energy study of "oriented and relaxed" polystyrene in the glassy state [J].
Embery, J. ;
Graham, R. S. ;
Duckett, R. A. ;
Groves, D. ;
Collis, M. ;
Mackley, M. R. ;
McLeish, T. C. B. .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2007, 45 (04) :377-394