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94 Tackifiers
1,3-pentadiene comonomer moiety or an aromatically-modified aliphatic tackifier having
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a dicyclopentadiene moiety.
A silicone rubber composition for adhering a semiconductor chip (die) has improved
reliability and adhesiveness by comprising a silicone resin having a vinyl group (the
weight average molecular weight in the range of 100,000 to 130,000), hydrogen polysilox-
ane (the weight average molecular weight in the range of 2,000 to 6,000.), a tackifier
(organopolysiloxane having epoxy functional group as the adhesive imparting agent),
spherical silicone particles having a specific reactive functional group, an inorganic silica
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filler, a hydrosilylation reaction catalyst, and a reaction retardant.
Cashew nutshell liquid contains a large concentration of cardanol and cardols, a nat-
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ural source of meta-substituted alkylated phenols and resorcinols. It is a globally avail-
able bio-renewable commodity, which makes it an ideal building block for the
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manufacturing of phenol-modified hydrocarbon resins. Due to the structure of the com-
ponents of cashew nutshell liquid, the hydrocarbon resins can be manufactured with fewer
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steps. The cardanol-based hydrocarbon resins have low viscosity, improved solubility in
organic solvents, very low cloud points, and compatibility with a great number of resins
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and polymer formulations. This makes them suitable additives as non-reactive diluents
for solvent-free coating formulations; tackifiers for structural, pressure sensitive, and hot-
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melt adhesives.
Polyamide resins used in preformed thermoplastic pavement marking compositions
are unstable and often disintegrate in the presence of alkaline (pH of 8 or greater) environ-
40
ments. Replacement of polyamide by ethylene vinyl acetate copolymer renders stable
compound which contains 5 to 15 wt% of a tackifier resin that is a rosin ester (e.g., Sylva-
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cote 4981).
Numerous examples of technological processes including tackifiers have been dis-
cussed in this section. The references are not exhaustive but representative of known tech-
nical discoveries, which mostly concentrate on the use of tackifiers in the pressure-
sensitive adhesives.
REFERENCES
1 H ö f e r , R , The Pine Biorefinery Platform Chemicals Value Chain, Industrial Biorefineries and White
Biotechnology, Elsevier, 2015, pp. 127-55.
2 Kumooka, Y, Forensic Sci. Int., 176, 111-120, 2008.
3 Kumar, KD; Tsou, AH; Bhowmick, AK, Int. J. Adh. Adh., 30, 200-7, 2010.
4 Sasaki, M; Fujita, K; Adachi, M; Fujii, S; Nakamura, Y; Urahama, Y, Int. J. Adh. Adh., 28, 372-81, 2008.
5 F i n k , J K , Terpene Resins. Reactive Polymers Fundamentals and Applications, 2nd Ed.,
WilliamAndrew, 2013, pp. 303-15.
6 Chong, KCW; Winnik, MA; Gong, L-z; Nowicki, J, Dyes Pigments, 79, 200-4, 2008.
7 Kong, W-S; Ju, T-J; Park, J-H; Joo, S-R; Yoon, H-G; Lee, J-W, Int. J. Adh. Adh., 38, 38-44, 2012.
8 Kim, B-J; Kim, S-E; Do, H-S; Kim, S; Kim, H-J, Int. J. Adh. Adh., 27, 102-7, 2007.
9 Raja, PR; Hagood, AG; Peters, MA; Croll, SG, Int. J. Adh. Adh., 41, 160-170, 2013.
10 Akiyama, S; Kobori, Y; Sugisaki, A; Koyama, T; Akiba, I, Polymer, 41, 4021-7, 2000.
11 Moon, S-h; Swearingen, S; Foster, MD, Polymer, 45, 5951-9, 2004.
12 Kumooka, Y, Forensic Sci. Int., 163, 132-7, 2006.
13 Ploeger, R; de la Rie, ER; McGlinchey, CW; Palmer, M; Maines, CA; Chiantore, O, Polym. Deg. Stab.,
107, 307-13, 2014.
14 Nakamura, Y, Adachi, M; Tachibana, Y; Sakai, Y; Nakano, S; Fujii, S; Sasaki, M; Urahama, Y,
Int. J. Adh. Adh., 29, 806-11, 2009.
15 Khan, I; Poh, BT; Mater. Design, 32, 2513-9, 2011.
16 Pernecker, T; Holmes, CJ; Quinlan, LE, WO2014200567, Arizona Chemical Company, Llc, Dec. 18, 2014.
17 Bao, H; Low, Y-G, WO2015135113, Henkel (China) Company Limited, Sep. 17, 2015.