US2004152824A1PendingUtilityA1

Surfactant-containing insulation binder

Priority: May 31, 2001Filed: Nov 17, 2003Published: Aug 5, 2004
Est. expiryMay 31, 2021(expired)· nominal 20-yr term from priority
C03C 25/285C08K 5/06
34
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Claims

Abstract

A fiberglass insulation binder composition made from a polycarboxy polymer, a polyhydroxy crosslinking agent, and a cationic surfactant, amphoteric surfactant, nonionic surfactant, or mixture thereof. Also, a process for manufacturing a fiberglass insulation product, which involves a step of applying the binder composition onto a fiberglass substrate and curing the fiberglass substrate so treated. Binders produced in accordance with the present invention are characterized by improved atomization, improved binder dispersion and fiber wetting properties, and improved protection of individual fibers during processing.

Claims

exact text as granted — not AI-modified
What is claimed is:  
     
         1 . A fiberglass insulation binder composition comprising a polycarboxy polymer, a polyhydroxy crosslinking agent, a mineral oil dust suppressing agent, a surfactant selected from the group consisting of cationic surfactants, amphoteric surfactants, nonionic surfactants, and mixtures thereof, and sufficient water to provide a mixture comprising up to 98 wt-% water based on the total weight of solids in the mixture.  
     
     
         2 . The fiberglass insulation binder composition of  claim 1 , wherein the surfactant is a nonionic surfactant selected from the group consisting of: ethylene oxide and propylene oxide condensates which include straight and branched chain alkyl and alkaryl polyethylene glycol and polypropylene glycol ethers and thioethers; alkylphenoxypoly(ethyleneoxy)-ethanols having alkyl groups containing 7 to 18 carbon atoms and having 4 to 240 ethyleneoxy units; polyoxyalkylene derivatives of hexitol; partial long-chain fatty acids esters; condensates of ethylene oxide with a hydrophobic base formed by condensing propylene oxide with propylene glycol; sulfur containing condensates prepared by condensing ethylene oxide with higher alkyl mercaptans or with alkylthiophenols wherein the alkyl group contains 6 to 15 carbon atoms; ethylene oxide derivatives of long-chain carboxylic acids or oleic acids or mixtures of acids; ethylene oxide derivatives of long-chain alcohols; and ethylene oxide/propylene oxide copolymers.  
     
     
         3 . The fiberglass insulation binder composition of  claim 2 , wherein the surfactant is an ethoxylated 2,4,7,9-tetramethyl-5-decyn-4,7-diol surfactant.  
     
     
         4 . The fiberglass insulation binder composition of  claim 1 , wherein the polycarboxy polymer is a polyacrylic acid polymer.  
     
     
         5 . A process for producing a fiberglass insulation binder comprising the steps of preparing a mixture of a polycarboxy polymer, a polyhydroxy crosslinking agent, a mineral oil dust suppressing agent, a surfactant selected from the group consisting of cationic surfactants, amphoteric surfactants, nonionic surfactants, and mixtures thereof, and sufficient water to provide a mixture comprising up to 98 wt-% water based on the total weight of solids in the mixture, and blending the mixture to form a polymeric composition useful as a fiberglass insulation binder.  
     
     
         6 . The process of  claim 5 , wherein the amount of surfactant employed ranges from about 0.01 to about 10 weight percent based on the total weight of binder solids.  
     
     
         7 . The process of  claim 6 , wherein the amount of surfactant employed ranges from about 0.2 to about 5 weight percent based on the total weight of binder solids.  
     
     
         8 . The process of  claim 5 , wherein a pre-mixture containing the polymer and crosslinking agent comprises about 50 to 60 wt-% water.  
     
     
         9 . The process of  claim 5 , further comprising the step of adding a hydrolyzed silane coupling agent to the mixture.  
     
     
         10 . The process of  claim 9 , wherein the weight of hydrolyzed silane coupling agent added is from 0.01 to 10 wt-% based upon the weight of the mixture.  
     
     
         11 . The process of  claim 1 , wherein the weight of mineral oil dust suppressing agent added is up to 20 wt-% based upon the weight of the mixture.  
     
     
         12 . The process of  claim 5 , wherein the polycarboxy polymer is a polyacrylic acid polymer.  
     
     
         13 . The product of the process of  claim 5 .  
     
     
         14 . A process for manufacturing a fiberglass insulation product, comprising: 
 (a) applying onto a fiberglass substrate, a binder composition comprising a polycarboxy polymer, a polyhydroxy crosslinking agent, a mineral oil dust suppressing agent, a surfactant selected from the group consisting of cationic surfactants, amphoteric surfactants, nonionic surfactants, and mixtures thereof, and sufficient water to provide a mixture comprising up to 98 wt-% water based on the total weight of solids in the mixture and    (b) curing the treated fiberglass substrate.    
     
     
         15 . The process of  claim 14 , wherein curing is carried out in a curing oven at a temperature from 200° C. to 350° C. for 30 seconds to 3 minutes.  
     
     
         16 . The product of the process of  claim 14 .  
     
     
         17 . A process for manufacturing a fiberglass insulation product, comprising: 
 (a) supplying melted glass to a fiber forming device;    (b) blowing said melted glass downwardly within a forming chamber of said forming device to attenuate glass fibers;    (c) applying the binder composition of  claim 1  onto said glass fibers;    (d) depositing said glass fibers onto a foraminous forming conveyor within said forming chamber;    (e) gathering and forming said glass fibers into a mat on said conveyor using a vacuum drawn through said mat from below said forming conveyor, wherein residual heat contained in said glass fibers and said vacuum volatizes said water; and    (f) curing the mat so treated.    
     
     
         18 . The process of  claim 17 , wherein curing is carried out in a curing oven at a temperature from 200° C. to 350° C. for 30 seconds to 3 minutes  
     
     
         19 . The product of the process of  claim 17.

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