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[½»Á÷] ¡¾ÇóÖú¡¿ Preparation of the PHSA-g-PMMA Comb Stabilizer

ÎÒÏëºÏ³ÉCore-shell PMMA latex colloids, ÔÚÕâÆÚ¼äÎÒÒªÓõ½Îȶ¨¼Á£¬ÕÒµ½Ò»Æª¹ØÓÚPHSºÏ³ÉµÄµ«ÊÇÓеĵط½²»Ì«Ã÷°×£¬Çë¸ß·Ö×ӵĴó¼ÒÃǸøÖ¸µãһϣºPreparation of the PHSA-g-PMMA Comb Stabilizer
In the first step,
47.9 g of recrystalized 12-hydroxystearic acid and 0.12 g of methanesulfonic acid are
dissolved into 8.53 g of toluene in a 250 mL flask, which is
equipped with a reflux condenser, a Dean-Stark trap, and a
magnetic stirrer. The reaction mixture is refluxed at 145-150
¡ãC under nitrogen, and toluene is used to remove the water
generated from polyesterification reaction by azeotropic distillation.
This reflux condition is maintained until the volume of
the collected water reaches a theoretical value of 2.3 mLand the
acid value of the final product is about 31.25 mg (KOH)/g
(polymer) determined by titration using 0.1mMKOHin methanol
so that the degree of polymerization of the polyester poly-
(hydroxystearic acid) reaches about 5-6
¼Ó´Ö²¿·ÖÓÐЩÒÉ»ó£¬ÔÚÈ¡1¿Ë·´Ó¦ÑùÆ·½øÐвâÁ¿Ëá¶Èʱ£¬ÊDz»ÊÇÐèÒª °ÑÑùÆ·Öеļױ½ºÍ²ÐÁ¿Ë®¶¼Õô³ö²ÅÄÜÓÃÇâÑõ»¯¼ØµÎ¶¨Ñ½£¿»¹ÊÇÖ±½ÓÈ¡1¿Ë»ìºÏÎï½øÐе樣¿
Finally, about 47.72 g
of poly(hydroxystearic acid)(PHSA)solution with93%nonvolatile
content in toluene is collected. Thus, the teeth on the comb
stabilizer are ready for the next step.
In the second step, 46.76 g of xylene, 0.05 g of hydroquinone,
0.14 g of Armeen DMCD, and 5.85 g of glycidyl methacrylate are
added into the same flask containing 47.7 g of PHSA solution
from the previous step. The reaction mixture is refluxed again
at 140 ¡ãC so that the carboxyl group on the poly(hydroxystearic
acid) is converted to a methacrylate group. The reaction is ended
when the acid value reaches 0.15 mg/g (nonvolatile solid) and
the final reaction mixture contains 50.5% nonvolatile content,
which is PHSA-GM
Õâ¸ö·´Ó¦ÖÕµãÎÒÒ²ºÜÃԻ󣬷´Ó¦ÌåϵһֱÊÇ»ìºÏÎËùνµÄ1¿Ëδ»Ó·¢ÎÊDz»ÊÇÐèҪȡһЩÑùÆ·È»ºó¹ýÂ˳öδ»Ó·¢Îï½øÐеζ¨Ñ½£¿
In the final step, to produce a monodisperse comb stabilizer,
the monomers are fed into a reaction medium, which is a mixture
of ethyl acetate and butyl acetate with a weight ratio of 2:1. A
25.6 g mixture of ethyl acetate and butyl acetate is first filled
into a 250 mL flask and heated to 80 ¡ãC. Then a mixture
containing 49.15 g ofPHSA-GMsolution from the last step, 44.89
g of MM and MA monomers (98:2 w/w), and 0.375 g of ADIB is
precisely pumped into ÕâÊDz»ÊÇÐèÒªÒ»ÖÖÌØÊâÒÇÆ÷ѽ£¿the flask over a period of 3 h. After the
feeding is completed, the reaction is maintained at 82-84 ¡ãC for
another 2 h. The final product is slightly brown in color. To
maintain it in a flowable solution at room temperature, the comb
stabilizer solution is diluted to 44.1% by adding more ethyl acetate
and butyl acetate.
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[ Last edited by chentp on 2008-7-28 at 22:08 ]
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