104.5 g of demineralized water were mixed with 562.5 g of acrylic acid (99.8%) pure and also 1246.0 g of 25% aqueous sodium hydroxide solution, 5.63 g of 1% aqueous methylene bisacrylamide, 1.25 g of 40% aqueous Trilon® C and 3.38 g of 1% aqueous Rongalit® C in a stirred vessel to form an aqueous phase. A second sealed stirred vessel (2 liter HWS equipped with anchor stirrer) was charged with 500 g of Shellsol® D 70 (100%) and 70 g of Emulan® GOE (100%) to form an organic phase, into which the aqueous phase was metered.
The combined aqueous and organic phases were then pre-emulsified in the second stirred vessel at 400 revolutions per minute for 60 minutes at 31° C. in a (15 liters/hour) stream of nitrogen and with bath immersion for temperature control. Thereafter, the speed of the stirrer was reduced to 200 revolutions per minute and 3.94 g of 10% aqueous sodium persulfate solution were added.
The polymerization kicked off immediately. When the internal temperature reached 35° C., the temperature-controlling bath was removed. The internal temperature reached a maximum of 66.2° C. After the temperature had decreased by 1° C., 28.13 g of 10% aqueous sodium persulfate solution was added followed 10 minutes later by 19.69 g of 1% aqueous Rongalit solution.
After the emulsion had cooled down, 12.5 g of Denacol EX 810 were added to it and the emulsion was mixed through at 200 revolutions per minute for a further 5 minutes. This gave an emulsion of mineral oil, water, carboxyl-rich acrylic acid copolymer and crosslinker.
A polyester needlefelt nonwoven fabric having a basis weight of 280 g/m2 was saturated with the emulsion prepared in Example 1. A pad-mangle was used. The pad-mangle consisted of a trough filled with the emulsion and two stripping rolls having confining walls on the side. The fabric was led through the pad-mangle at a speed of 1 meter per minute. The emulsion-loaded fabric was dried at 170° C. for 5 minutes. The absorbent composite had a basis weight of 410 g/m2, the weight increase (solids add-on) was 46%.
The absorbent composite was placed in water and an hour later the water uptake was determined by weighing back. The fabrics were further tested manually for hydrogel ooze and hence for leaching losses from the fabrics after particular times. A wetting test was carried out in addition. To this end, a droplet of water was applied to the surface of the absorbent composite and the time taken for the drop to disappear from the surface was measured. The results are summarized in Table 1.
Example 2 was repeated using nonwoven polyester quilting having a basis weight of 80 g/m2.
Number | Date | Country | Kind |
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102004005418.5 | Feb 2004 | DE | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP05/00897 | 1/29/2005 | WO | 00 | 7/24/2006 |