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Mark, Polymer Data Handbook
1. 995
Poly(1,3-trans-ε-carboxyphenoxypropane anhydride)
Jagath K. Premachandra, Chamdima Kumudinie,
and Junzo Masamoto
Acronym, Trade Names Bore conullut ulput nit, sed magna feugiamcorer am venissi
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Structure −[CH2−CH=CH−CH2]m−[CH2−CH]n−
|
C=N
Major Applications Bore conullut ulput nit, sed magna feugiamcorer am venissi exercinim
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Source(4) Cellulose (%)
Cotton 94
Hemp 77
Flax 75
Straw 40–50
Gelatin Testing Methods
Identification Gelatin gives the normal positive trichloroacetic acid, biret, ninhydrin.
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Thermal behavior(1)
Cis isomer 1. Cis to trans isomerization at 145°C
2. Molecular rearrangement at 325°C
3. Thermal decomposition at 420°C
Shorthand notation for siloxane polymer units
Formula: (CH3)3SiO0.5 (CH3)2SiO (CH3)SiO1.5 SiO2
MDTQ formula: M (monofunctional) D (difunctional T (trifunction) Q (tetrafunctional)
CH3 CH3 CH3 O
| | | |
H3C–Si–O– –O–Si‑O– –O–Si‑O– –O–Si‑O–
| | | |
CH3 CH3 O O
2. Poly(1,3-trans-ε-carboxyphenoxypropane anhydride)
997996
Poly(1,3-trans-ε-carboxyphenoxypropane anhydride)
P2O5 (wt. %) [P2O5] 1 2 3 4 5 6 7 8 9 10 11 12 13 14 High-Poly
89.4 1.066 1.88
89.4 1.066 1.88 1.52
89.4 1.066 1.88 1.52 0.77
89.4 1.066 1.88 1.52 0.77 0.61
89.4 1.066 1.88 1.52 0.77 0.61 0.62
89.4 1.066 1.88 1.52 0.77 0.61 0.62 0.68 0.54
89.4 1.066 1.88 1.52 0.77 0.61 0.62 0.68 0.54 0.71
89.4 1.066 1.88 1.52 0.77 0.61 0.62 0.68 0.54 0.71 0.86 1.03
89.4 1.066 1.88 1.52 0.77 0.61 0.62 0.68 0.54 0.71 0.86 1.03
89.4 1.066 1.88 1.52 0.77 0.61 0.62 0.68 0.54 0.71 0.86 1.03 0.98
89.4 1.066 1.88 1.52 0.77 0.61 0.62 0.68 0.54 0.71 0.86 1.03 0.98 1.16
89.4 1.066 1.88 1.52 0.77 0.61 0.62 0.68 0.54 0.71 0.86 1.03 0.98 1.16 1.23 1.37 86.8
89.4 1.066 1.88 1.52 0.77 0.61 0.62 0.68 0.54 0.71 0.86 1.03 0.98 1.16 1.23 1.37 86.8
89.4 1.066 1.88 1.52 0.77 0.61 0.62 0.68 0.54 0.71 0.86 1.03 0.98 1.16 1.23 1.37 86.8
89.4 1.066 1.88 1.52 0.77 0.61 0.62 0.68 0.54 0.71 0.86 1.03 0.98 1.16 1.23 1.37 86.8
89.4 1.066 1.88 1.52 0.77 0.61 0.62 0.68 0.54 0.71 0.86 1.03 0.98 1.16 1.23 1.37 86.8
89.4 1.066 1.88 1.52 0.77 0.61 0.62 0.68 0.54 0.71 0.86 1.03 0.98 1.16 1.23 1.37 86.8
89.4 1.066 1.88 1.52 0.77 0.61 0.62 0.68 0.54 0.71 0.86 1.03 0.98 1.16 1.23 1.37 86.8
Property Units Conditions Value Reference
Density g cm–3 26-27% ACN 0.92 (1)
Glass transition temperature Tg K ~20% ACN 213 (2)
~30% ACN 231
~34% ACN 238
Service temperature (max) K 9% N
Solubility Parameter (MPa)1/2 25% ACN, 25˚C, calc. 18.93 (4)
Theta temperature θ K 26% ACN, cyclohexane/MEK (64/36) 293.2 (5)
40% ACN, cyclohexame/MEK (52.5/47.5) 295.2
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Synthesis(1–4)
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Other physical properties(4)
Property Polymer Conditions
Color [Si(Pc)O]n Dark purple powder
Solubility [Si(Pc)O]n Concentrated H2SO4 and HSO3CH3:
0.013 g in 25 ml concentrated H2SO4 at room temperature
0.020 g in 25 ml concentrated H2SO4 at 80C
Densities
Density (G CM –3)
Polymer y Calculated Found Reference
[Si(Pc)O]n — 1.458 1.432 (4,6)
Sonic velocity Infrared diachroic
X-ray angle (degree)
Thickness Density Birefringence
(ms–1) ratio (at 730 cm–1) a-axis b-axis
(μm) (g cm–3) (× 103) MD* TD* MD/TD* MD-TD* ND-MD* MD-TD* ND-MD*
54 0.9182 –9.79 953 1,128 1.15 45–50 45–60 0 0
26 — –8.23 870 1,003 0.88 45 45–60 0 0
23 0.9175 –3.07 852 998 1.13 70 60–70 0 0
Table 2. This page uses 30 pts r/b above “Densities” head abd 24 pts between other blocks.
This text ignores far right TSH so 24 pts b/b is to 2nd row.
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Typical properties of filled amino resin molding compounds(3)
Urea Melamine
Property Units Alpha-cellulose Alpha-cellulose Asbestos Glass fiber
Physical
Specific gravity _ 1.47–1.52 1.47–1.52 1.7–2.0 1.8–2.0
Water absorption % 0.48 0.1–0.6 0.08–0.14 0.09–0.21
Mechanical
Tensile strength MPa (103) 38–48 (5.5–7) 48–90 (7–13) 38–45 (5–6.5) 35–70 (5–10)
Elongation % 0.5–1.0 0.6–0.9 0.3–0.45
Tensile strength MPa (103) 38–48 (5.5–7) 48–90 (7–13) 38–45 (5–6.5) 35–70 (5–10)
Thermal
Tensile strength MPa (103) 38–48 (5.5–7) 48–90 (7–13) 38–45 (5–6.5) 35–70 (5–10)
Elongation % 0.5–1.0 0.6–0.9 0.3–0.45
Tensile strength MPa (103) 38–48 (5.5–7) 48–90 (7–13) 38–45 (5–6.5) 35–70 (5–10)
3. Poly(1,3-trans-ε-carboxyphenoxypropane anhydride)
999998
Poly(1,3-trans-ε-carboxyphenoxypropane anhydride)
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fE 0.06 0.15 0.31 0.37 0.42 0.49 0.70 0.77 0.90 1.00
pK* 6.08 5.70 4.90 4.70 4.55 4.50 4.40 4.35 4.35 4.35
pK† 6.61 5.92 5.03 4.80 4.48 4.40 4.35 4.40 4.55 4.70
fE 0.06 0.15 0.31 0.37 0.42 0.49 0.70 0.77 0.90 1.00
pK* 6.08 5.70 4.90 4.70 4.55 4.50 4.40 4.35 4.35 4.35
pK† 6.61 5.92 5.03 4.80 4.48 4.40 4.35 4.40 4.55 4.70
fE 0.06 0.15 0.31 0.37 0.42 0.49 0.70 0.77 0.90 1.00
pK* 6.08 5.70 4.90 4.70 4.55 4.50 4.40 4.35 4.35 4.35
pK† 6.61 5.92 5.03 4.80 4.48 4.40 4.35 4.40 4.55 4.70
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Conditions
Time
(days)
Value
(% mass loss day–1)
Time
(days)
Value
(% mass loss day–1)
Insulin loadings at 40% in copolymer at
pH = 2.09; S.D. ± 3; error 10%
0.0 0.0 5.1 96.4
0.07 9.0 7.1 98.8
0.1 25.4 9.0 98.9
0.3 49.0 12.0 99.5
3.0 85.5 25.0 100.0
4.0 89.4
Ditto (aat 10% loading) 0.0 0.0 5.1 96.4
0.07 9.0 7.1 98.8
0.1 25.4 9.0 98.9
0.3 49.0 12.0 99.5
3.0 85.5 25.0 100.0
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Chemical shift (ppm) Chemical shift (ppm) Chemical shift (ppm) Chemical shift (ppm)
Sequence Sequence Seqiemce Carbon
Butene assignmnet* Hexene assignment* Octene assignment* 4-MP-1 assignment*
35.0 BBB 38.13 EHE 32.22 EOE 34.6 alpha-C
34.5 EBEB + BEBE 35.85 EHH + HHE 30.47 OEEE + EEEO 25.8 2-C
39.56 BBBE + EBBB 40.86 EHE + EHH + HHE + HHH EOE + EOO + OOE + OOO
10.81 BBB 27.09 HHEE + EEHH
24.39 EHEHH + HHEHE
Figure 1. PAMAM dendrimers as a function of shape, core, branch cell and terminal groups, where:
Nb=branch cell multiplicity, Nc=core multiplicity and G=generation.
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Other uses
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henisi. Ilit ut utet wisit, quat.
■ Ut aliquamet, sum elesendiamet dionsecte modolortio ercing ea alis.
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consequis augiamc onsequat nostrud minciduisi.
Suppliers
EMS Chemie AG, Domat, Switzerland
Elf Atochem S.A., Paris, France
UBE Industries, Tokyo, Japan
Creanova GmbH., Division of Degussa-Hüls AG., Marl, Germany
References
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henisi. Ilit ut utet wisit, quat.
2. Ut aliquamet, sum elesendiamet dionsecte modolortio ercing ea alisl ut lam venibh
erosting eliquam in utem veriurerat ipsusci liquis.
3. Exeriliscil ing eliquissis augueri usciliquam ent num qui tem estrud dolenisissi ex endio
consequis augiamc onsequat nostrud minciduisi.
Acknowledgment
The author wishes to acknowledge McWhortyer Technologies fo rits generous support in
compiling these data.