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FUNDAMENTALS OF PLASTICS

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发表于 2014-7-16 18:41 | 显示全部楼层 |阅读模式
本帖最后由 青华专业ug培训 于 2014-7-16 18:54 编辑
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FUNDAMENTALS  OF   PLASTICS
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Why Plastics

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Complex parts in one operation
+ o( K) Z+ S: I3 [: J; }Wide range of properties
& o3 ?, f$ j* f" ~3 D( `Coloring
; r% i- P0 ]$ e9 X) h- h/ xLow energy requirements/ B* k: B( B+ v" d) X/ ?) [
Good insulators
9 h3 a9 M% V% G/ f0 M8 V" tLow cost & weight! F* X: Y# \/ _1 w6 Q  O3 i: M; w
Resistance to chemicals1 ~- l" X1 f9 q9 m: [% P8 X
From monomers to polymers        9 p) P2 q* e: [
Examples : (in between   : monomer )
/ z9 F3 @& d( Q% v8 ZPolyethylene:  (catalytic polymerization of ethylene gas  under high pressure)
: E3 ~2 o$ I2 }8 h  |5 h; X      —CH2 — CH2-- CH2 — CH2 -- CH2 —
8 T6 C/ c$ b! B5 i8 N% J1 \$ }1 mPolypropylene: (catalytic polymerization of propylene gas under pressure)
4 f. O6 i: s' T      —CH2 — CH-- CH2 — CH -- CH2 — 2 {0 c2 l1 o- ]& Y9 V0 E
                     CH3                       CH3, {6 V8 {  l. b$ H/ d+ u; g
Polyvinylchloride :
; o8 h5 }2 R# l; b0 ?     — CH2 — CHCl -- CH2 — CHCl -- CH2 — CHCl — 5 |' ?9 A  p" z7 o; i8 _

$ D9 A' m! N/ U3 o" w4 HMolecular weight        
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QQ截图20140716183155.jpg
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Polymer structures0 h- D+ o/ W4 i4 Z) o
Homopolymers (ie PP homo)
: Z" }2 n  l0 A5 `# FCopolymers (ABS, SAN)% |# d$ y! n6 @6 ?; a  H
random  Z1 Y4 o) M; ~0 |0 f7 x
regular
* j* N) ?8 d3 e; p8 R3 I4 M/ usequenced
/ z  p. R, Y' a& tlinear
7 s/ q* A5 ^2 j9 |+ N9 Egrafted
; S) Q! c' h! X4 ~0 I/ JBlends and alloys
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Polymer structures        
* B! y6 Z" }" A" [1 V( JWhy using Blends and alloys?
8 M3 O3 K1 H( `. U. l  v  cTo combine properties of different polymers.! A$ T" n1 x+ F5 M
Examples: what brings each polymer in                 blends below?
0 n# f, F/ K. E' ^5 H2 `% VABS/PC
7 W& ]8 p: A# m) d0 {! K/ ZPC/PBT
& z' Y3 N$ h# e* ~2 [* OPPO/PS
; D6 I% P+ U$ Y, q- @, HPA/PPO
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Polymer structures        
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Crystalline vs Amorphous resin
% K& C0 Z" C: l8 g  C( uAre the resin different?) y2 v& e( H+ |: a$ W
Are the resin processed the same way?0 H, \0 H7 F. Q+ y/ e
Can the resin be used in the same applications?
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Amorphous resin, ~6 e3 m0 Q! j% {+ T+ M
Non organized structure% z5 B" w; t) n* H
Broad softening range: 20°C- d( n; s$ m# o6 ?# R- I
High viscosity usually6 t* i3 }  b) V# X/ D; b
Poor chemical properties in general
! d& d) B  V0 s: j& z' y+ ECan be transparent
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Amorphous resin9 k+ V' r. u. I: c: v$ c$ r* U

, A7 @! ]$ c( U! w QQ截图20140716183421.jpg
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4 v' b+ D& k6 L) q* @Crystalline resin
, u! Y) D4 Z* o2 POrganized structure5 Y) l5 r/ _& v0 k/ [0 {

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" z& Q( r5 B2 @9 ]- JMelting point: within 5°C
; J. l( v: y& G+ k1 X$ TLow viscosity usually. i. ^) D. F% R4 {4 U
Good chemical properties in general
% z  ]4 b* \) H8 y0 xUsually not transparent
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Crystal structures (1)  h4 A$ O  X$ J$ I
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Crystal structures: the unit cell (2)
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" I# y9 o( @( Q' h9 F$ T7 BMacro structure: the spherulite (1)
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; [7 g, x0 I/ S' v. xMost of the semi-crystalline resins crystallize into a spherulitic macro structure. The macromolecules loop on themselves to shape a lamella. The lamellas are assembled into a spherical super structure called spherulite. The spherulite is growing from a center point, the nucleation point.
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图片1.png
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7 y( ?! G; O/ V  l0 A" D  EMacro structure: the spherulite (2)% |  a( P! N8 z/ ^0 S
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The crystalline entities can also be discs or rods. Once the crystalline entities growth is blocked up by other crystralline entities, the primary crystallization is over and start the secondary crystallization between crystalline entities or lamellas.4 V, v& S$ y' t9 e1 m. V
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Macro structure
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Crystalline resin
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QQ截图20140716184459.jpg
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Semi-crystalline resin: G2 k$ @) O5 T

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) }! w9 E1 |7 z" PSemi-crystalline vs amorphous resin (DSC)
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QQ截图20140716184622.jpg
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5 h, R  X7 [& }, a* A* u# kTg and Tm: some examples
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: m) z; t6 A* ?' DTypical process temperatures0 W; n9 B  s9 Q0 A- w3 d
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) _# A' p4 s* `Physical properties! J  S9 Z" t/ s0 k

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' o3 ?% u' G8 x5 B/ ]Thermoplastic families / Applications
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3 v4 B) ]* h0 r+ S$ X( X4 R& f, gThermoplastic families / Applications ' W; p- n9 J- G

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0 [0 S* V* L  V8 y" Z3 BThermoplastic families / Applications * q# Y+ _/ S" l/ l, C( r0 Q

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 楼主| 发表于 2014-7-16 19:01 | 显示全部楼层
Thermoplastic families / Applications
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Thermoplastic families / Applications / where to focus
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6 x" ?  r8 W- ~. d9 n& y! XAdditives' z& `# y+ p. m- v. @

$ T3 n7 ]9 {: I2 F7 ?Plasticizers (Phtalates in PVC)
. G9 B; q% u- ?0 V0 `" ~. uStabilizers (UV stabilizer, carbon black)
0 J# ?, l/ b& M- sColorants
3 I# A# j- l* c) HNucleating agents (Talc in PP)8 H) K5 w/ H, a0 s
Fillers (Talc in PP)2 k9 y' h  G: o! {" k
Reinforcements (GF, CF, Kevlar)4 O: x4 @* W. V5 t4 o) i' x
Lubricants (Calcium stearate)
, s+ ?4 I8 _" }, {Plasticizer
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Nucleating agent effect3 ^% u0 q+ K! |& y5 H$ f
QQ截图20140716185815.jpg
# [! H4 M2 C# mFillers
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7 G. A% M' [- X: c5 [3 ]* XPurpose
& v. F6 A3 F% eDimensional stability' |- ]: ^5 z' G2 V+ f- v! g/ Q( X8 O
Rub- resistance
  @; N; B- C$ j$ Y5 pCompressive strength5 v4 X, [( B* T, G7 E
Cost; q- a% E: y( m
Materials; A% M* }& Y, L4 ~" ]
Calcium Carbonate
" W! x( o+ u% G, BGlass beads# [' L3 I7 ]5 L# ^
Talc, Mica, Glass flakes; f# ^; c- Q5 L1 D, \
Reinforcements3 P8 Y0 j' T+ X1 j1 ~

8 y3 _! s- o& |8 cPurpose
$ Z# p: x1 S1 j$ |8 I# aTensile Strength
$ i0 e* {3 v; I/ J, Z: h& {$ FImpact Strength7 l8 M- h! ~& P: z9 I' O
Heat Deflexion Temperature (HDT)
0 ^9 v' _; k- RTensile Modules* ]( h- W9 ?* A) \8 h
Materials
# f7 Z7 j5 a$ L# w0 xGlass Fibers7 q: q' Z* J, g, \$ Y+ h5 y
Carbon Fibers
( W2 h" N) I) LTalc
. i$ H7 m3 m; i! Q4 G% ^Consequences on processing3 x& u0 L1 U( T# W2 ~; f  e
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5 a1 q" K# T6 XConsequences on processing
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Flow Behavior  A# B; k5 m& V% E* l

; K8 K; A9 a& n. w/ N, RViscosity
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Temperature Rise & Residence Time+ |) Z, V" K- C% _& ^
degradation
6 d! V) L. U/ D$ ^3 ^/ dViscosity
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' n# g6 V; {) e  x2 iResistance to flow* Z) v. ^# g( g
If a force is applied to a liquid, the rate of flow is a measure of viscosity.
# h' K* j) x& ?5 U1 `Rapid flow = low viscosity liquid
2 P+ Z$ \) D  i# G7 M$ ESlower flow = high viscosity liquid
0 R* x) k% Y. j& MUsually the viscosity is given in Pa.s4 ~% g" }- U5 U3 f7 V) P" j0 r
Do not confuse with MFR or MFI; P& ~7 ]" r; m
Viscosity / MFR
# Q, j4 k7 B8 x% E) x& {# n QQ截图20140716190107.jpg
图片2.png
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 楼主| 发表于 2014-7-16 19:06 | 显示全部楼层
Viscosity / MFR
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8 _5 q3 v1 {) j3 JExample:
! R. d& _/ d" S, I9 h% N( xPolycarbonate PC:        MFR 12$ C4 w  j9 O! T; b& k
Test conditions:        Temperature 300°C
5 ]* j2 T- Y4 Z5 D; ?7 x                                Load 10 kg
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Polypropylene PP:         MFR 12
( Z7 h( K% ]) q2 I; C* l- b* UTest conditions:        Temperature 230°C
; P0 a7 L8 [) E! x' O                                Load 2.16 kg' a" u. K5 e# A  L4 A! ]
Shear rate4 s& u& x4 X5 z2 o

% i& ^/ N# l# c- Q2 GWhat is the shear rate?
, Q/ c2 R* f! Y/ d( x( o6 m/ N7 aIf we consider a laminar flow (we have a problem  if the plastic flow is not laminar!). The shear rate can be described as the speed difference between 2 layers.
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5 {; i- T6 R/ D& T6 E% K0 wShear rate
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' G- F* z& v7 M' j( tThe resin speed is minimum (almost 0 in the HR channels, normally 0 in the tool cavity) at the wall contact and maximum in the middle of the flow. The shear rate is maximum where dV/dY is maximum.
$ y: z; u; [7 I0 S9 LWhat happen if the shear is too high?
, O8 Y2 ?' g6 s- D! g/ Z6 ]3 Y/ A QQ截图20140716190319.jpg
  b8 r& {& {& E! D# J: U# E* ]; ONewtonian Fluids
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Non-Newtonian Fluids
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Viscosity vs shear rate2 ^4 b3 \( M2 Q9 f4 r! |
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Viscosity vs shear rate
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# y5 D- ?, x) O, Z* [. iViscosity vs molecular Wt.% l: f( A/ I8 e( P- u
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