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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

Inactive Publication Date: 2012-12-06
ECOSYNTHETIX INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

"The patent describes a new way to make various fiber products using a combination of biopolymer nanoparticles and a curable binder. The use of biopolymer nanoparticles allows for improved bonding with the fibers, resulting in stronger and more durable products. The curable binder composition includes a multifunctional crosslinking agent that can react with the nanoparticles and the fibers to form a network of bonds. This crosslinking agent can trigger in the curing stage to lock in the desired fiber mat dimensions. The patent also describes a method for making non-woven materials and binding together glass fibers using the new binder composition. The technical effects of this invention include improved bonding strength, durability, and flexibility in the production of various fiber products."

Problems solved by technology

A serious disadvantage of formaldehyde-based resins is the release of free formaldehyde to the environment during manufacturing and use, contaminating the air that we breathe which is undesirable for health and ecological reasons.
In addition to the health and environmental problems, further compounding the problem is that the lowest cost formaldehyde based binders are based on UF resins.
These resins are typically used in outdoor applications, and therefore their main challenge is worker exposure during manufacturing, while in-use release of formaldehyde is less of a concern, especially in outdoor applications.
However, traditional biobased industrial materials derived from agricultural crops are generally viewed by manufacturing and packaging industries as less consistent and inferior to the dominant petrochemical-based synthetic products.
However, these have serious shortcomings such as high cost, high corrosivity, high viscosity, dark color, lack of rigidity, water sensitivity, poor bond strength, etc.
This technology has been found to result in major corrosion problems with the equipment used to manufacture fiberglass insulation products, as well as in-use applications where metal wall studs and other metal components are being used in combination with the fiber glass insulation product.
The problem is the much higher cost of PVOH relative to conventional formaldehyde binder systems.
In addition, since it is petroleum based it is a carbon positive material which is not environmentally preferred.
Without any additional enhancer, this binder does not provide sufficient wet strength and water resistance.
The major disadvantage of this binder is high cost and low pH which causes corrosion of fiber glass mat production equipment and during in-use applications.
Disadvantages of this system are low pH and high viscosity at relatively low solids content.
The problems as mentioned above include the much higher cost of PVOH relative to conventional formaldehyde binder systems, and since it is petroleum based it is a carbon positive material which is not environmentally preferred.
This binder is also corrosive due to relatively low pH (about 4) and does not provide the required water resistance.
However, a practical use of such a composition for insulation production is limited because the high acidity of these binder compositions will cause corrosion of production lines and during the in-use applications.
Moreover, whilst the strength of this binder is acceptable for some applications it is not as good as the commonly used formaldehyde based binders.
In addition, since it is petroleum based it is a carbon positive material which is not environmentally preferred.
), which a serious disadvantage.
Such a system has relatively low water resistance, is dark in color and generates ammonia emissions upon cure.
In addition, since it is petroleum based it is a carbon positive material which is not environmentally preferred.
These binders turn dark brown on curing and have poor water and biological resistance.
While these references and other prior art systems disclose various formaldehyde-free systems for insulation and non-woven mats, they all have limitations with respect to developing binders that are effective as well as environmentally friendly.
These binders have limited application due to high cost.
In addition, they are petroleum based carbon positive materials which are not environmentally preferred.
A major problem in the manufacturing process and use of some known fiber mats is inadequate wet web strength.
But higher vacuum draw will lead to undesired mat properties, such as a high mat tensile ratio (i.e. the ratio of dry to wet tensile strengths).
Inadequate dry mat tensile strengths also can reduce the ability of the finished roofing product to resist stresses during its service lifetime on the roof.
A major problem in the manufacturing process and use of fiber mats is inadequate wet web strength, which cannot be provided by a urea formaldehyde resin without an additive, as illustrated by the related art described in this paragraph.
In addition, since these binders are all petroleum based they are carbon positive materials and therefore not environmentally preferred.
The main disadvantage of these binders is a necessity of preparing the binder before applying it on the glass fiber mat due to a limited stability of a resin / latex mixture.
In addition, since these binders are petroleum based they are carbon positive materials which are not environmentally preferred.
However, all of these to date have serious shortcomings such as high cost, high corrosivity, high viscosity, dark color, lack of rigidity, water sensitivity, poor bond strength, etc.
No inter-particle crosslinks exist, as this would result in poor rheology and reduced binding power (reduced surface area).
Currently, the industry consumes over 4 billion pounds of SB and SA latex per annum.
As the price of oil continues to escalate, and as the price of synthetic binders has increased by more than 100% over the past few years, paper producers have faced increased production costs forcing them to find efficiencies, pass increases on to the consumer, or cease production.

Method used

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  • Curable biopolymer nanoparticle latex binder for mineral, natural organic, or synthetic fiber products and non-woven mats
  • Curable biopolymer nanoparticle latex binder for mineral, natural organic, or synthetic fiber products and non-woven mats
  • Curable biopolymer nanoparticle latex binder for mineral, natural organic, or synthetic fiber products and non-woven mats

Examples

Experimental program
Comparison scheme
Effect test

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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Abstract

A curable aqueous binder composition includes a dispersion of biopolymer particles, optionally with and an inter-particle crosslinking agent, for use in the formation of composite materials such as mineral, natural organic, or synthetic fiber products, including mineral fiber insulation, non-woven mats, fiberglass insulation and related glass fiber products, and wood based products, and construction materials. In an application of the curable aqueous composition to making fiberglass insulation, the composition may be blended with a second resin which may be a non-formaldehyde resin. In an application of the composition to making fiberglass roofing shingles, the biopolymer particles may be mixed into a formaldehyde based resin during or after the polymerization of the resin.

Description

CROSS-REFERENCES TO RELATED APPLICATIONS[0001]This patent claims the benefit of U.S. provisional patent application No. 61 / 493,266 filed on Jun. 3, 2011 which is incorporated herein by this reference to it.STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH[0002]Not Applicable.BACKGROUND OF THE INVENTION[0003]1. Field of the Invention[0004]This invention relates to a curable composition, for example a composition useful for forming a composite material comprising biopolymer particles, and to composite materials, for example mineral fiber insulation and roofing shingles.[0005]2. Description of the Related Art[0006]The following discussion is not an admission that anything described below is common knowledge of persons skilled in the art, or citable as prior art.[0007]Mineral fibers used in insulation products and non-woven mats are usually bonded together with a crosslinked binder resin. The binder has to provide the resilience for recovery after packaging (in the case of insulation pro...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C09D103/00B32B17/04C09D197/02C09D161/24B82Y30/00
CPCC08J5/24D04H1/587C08J2303/04C08L61/24C08J2303/02C03B37/04B29C39/003C09J161/24C08L2205/18C08L2205/16C09J103/04C08K5/0025C08K7/04C08K7/14C08L97/02C08L1/02C08L89/00C08L67/00C08L23/00C08L33/08C08L77/00C08L77/02C08L3/04Y10T442/2992B27N3/04C08J5/244C08J5/249
Inventor TSEITLIN, ALEXANDERVAN ALSTYNE, DAVIDBLOEMBERGEN, STEVEN
Owner ECOSYNTHETIX INC