A washing-resistant flame retardant synergist for textiles and its preparation method and application
A flame-retardant synergist and washing-resistant technology, which is applied in textiles and papermaking, flame-retardant fibers, and liquid-repellent fibers, etc. To solve the problem of degradation, achieve excellent flame retardancy and water repellency, improve repeated use, and achieve the effect of durable flame retardancy
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Embodiment 1
[0051] Polyurethane emulsion formulation:
[0052]
[0053]Textile washing resistance flame retardant synergist formula:
[0054]
[0055] 1. Preparation
[0056] (1) Under the protection of inert gas nitrogen, react 30mol toluene diisocyanate with 10mol trimethylolpropane at 60°C for 1.5h to prepare -NCO group-terminated prepolymer I, and then add 2mol of N-methyl diisocyanate Ethanolamine and 1 mol of polyethylene glycol monomethyl ether 500 were reacted at 60°C for 2 hours to prepare prepolymer II (reacted to the set -NCO group content);
[0057] (2) The prepolymer II and 13mol of tribromoethanol were subjected to a capping reaction at 60°C for 2 hours to obtain the prepolymer III (reacted to the set -NCO group content), and then the prepolymer III was mixed with 12mol of methyl ethyl ketone The oxime was subjected to capping reaction at 60°C for 4h (reaction until the -NCO group content was set to zero), cooled to below 40°C and added 3mol acetic acid for neutraliz...
Embodiment 2
[0066] Polyurethane emulsion formulation:
[0067]
[0068] Textile washing resistance flame retardant synergist formula
[0069]
[0070] 1. Preparation
[0071] (1) Under the protection of inert gas nitrogen, react 30mol isophorone diisocyanate with 10mol trimethylolpropane at 60°C for 1.5h to prepare -NCO group-terminated prepolymer I, and then add 2mol of N- Methyldiethanolamine and 1mol of polyethylene glycol monomethyl ether 500 were reacted at 60°C for 2 hours to prepare prepolymer II (reacted to the set -NCO group content);
[0072] (2) The prepolymer II and 13mol of tribromoethanol were subjected to a capping reaction at 60°C for 2 hours to obtain the prepolymer III (reacted to the set -NCO group content), and then the prepolymer III was mixed with 12mol of methyl ethyl ketone The oxime was subjected to capping reaction at 60°C for 4h (reaction until the -NCO group content was set to zero), cooled to below 40°C and added 3mol acetic acid for neutralization rea...
Embodiment 3
[0081] Polyurethane emulsion formulation:
[0082]
[0083] Textile washing resistance flame retardant synergist formula:
[0084]
[0085] 1. Preparation
[0086] (1) Under the protection of inert gas nitrogen, react 30mol toluene diisocyanate with 10mol trimethylolpropane at 60°C for 1.5h to prepare -NCO group-terminated prepolymer I, and then add 2mol of N-methyl diisocyanate Ethanolamine and 1 mol of polyethylene glycol monomethyl ether 500 were reacted at 60°C for 2 hours to prepare prepolymer II (reacted to the set -NCO group content);
[0087] (2) Prepolymer II and 13mol of trichloroethanol were capped at 60°C for 2 hours to obtain prepolymer III (reacted to the set -NCO group content), and then prepolymer III was mixed with 12mol of methyl ethyl ketone The oxime was subjected to capping reaction at 60°C for 4h (reaction until the -NCO group content was set to zero), cooled to below 40°C and added 3mol acetic acid for neutralization reaction for 0.5h, and finall...
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