Curable biopolymer nanoparticle latex binder for mineral, natural organic, or synthetic fiber products and non-woven mats
a biopolymer nanoparticle and non-woven mat technology, applied in the field of curable composition, can solve the problems of contaminating the air that we breathe, inferior to the dominant petrochemical-based synthetic products, and the lowest cost of formaldehyde-based binders are based on uf resins, so as to facilitate the recovery of useful fiber mats and dry and wet tensile strength properties
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example 1
Preparation of Biopolymer Binder Composition
[0107]The technique described in U.S. Pat. No. 6,677,386 has been used to prepare biopolymer nanoparticles by reactive extrusion processing. Native potato starch, corn starch, tapioca and waxy corn starch have been used to prepare nanoparticles. Agglomerated particles of such nanoparticles are commercially available, sold under the trade mark Ecosphere, from Ecosynthetix Inc. Ecosphere 2202 extruded pellets comprised of starch nanoparticles were dispersed in water using mechanical agitation. The nanoparticles at 35% (w / v) solids were dispersed in 15 minutes at 45° C. using a 3-blade mixer at 200 rpm. A crosslinker (tetraethyl orthosilicate) was added in amount of 1 wt % (based on dry solids) and mixed for 30 minutes. After that the pH was adjusted to 7.0 with aqua ammonia. The binder is a low viscosity liquid. The stability of the resulting biopolymer binder is about 1 month at room temperature.
example 2
Preparation of Blends of Biopolymer Binder
[0108]Glass fiber binder compositions were prepared using the biopolymer of Example 1 mixed with 25, 40 and 50 parts (dry basis) of polyester as described in example 3 of WO 03 / 106561 at room temperature. A crosslinker (tetraethyl orthosilicate) was added in the amount of 1% by weight (based on dry solids) and mixed for 30 minutes. No crosslinker was added to the control binder compositions. After that the pH was adjusted to 7.0 with aqua ammonia. In addition, a glass fiber binder composition was prepared using the biopolymer of Example 1 mixed with 50 parts (dry basis) of polyacrylic binder as described in the example of U.S. Pat. No. 6,331,350 at room temperature. A crosslinker (tetraethyl orthosilicate) was added in the amount of 1% wt (based on dry solids) and mixed for 30 minutes. After that the pH was adjusted to 7.0 with aqua ammonia. No crosslinker was added to the control binder composition.
example 3
Tensile Testing of Cured Glass Fiber Specimens
[0109]The biopolymer binder composition of Example 1 prepared from dry EcoSphere® 2202 biopolymer latex powder to give a 35% solids dispersions was subsequently diluted with water to give a binder dispersion having 15% non-volatiles, and the binder solution was applied to a glass fiber substrate as follows. Glass paper (Whatman 934-AH) was soaked in the binder solution for 5 minutes, then the excess liquid was removed by vacuum. The samples were put into an oven at 200° C. for 5 minutes for curing of the binder resin. The cured samples were cut into specimens having the dimensions of 6″×1″ and tested for dry tensile strength by an Instron tensile tester. For wet tensile testing, the specimens were treated with hot water at 80° C. for 10 minutes, and then tested for tensile strength while still wet. The test results are presented in the Table 1, where Comparative A is polyester binder as described in WO 03 / 106561; comparative B is a pure ...
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