Flame-resistant polymer polyol dispersion

Abstract

The invention relates to a process for preparing a flame-resistant polymer-modified polyol having a solids content of 1 to 65 wt. % wherein (i) at least one polyisocyanate and (ii) an olamine are reacted in (iii) a base polyol having at least two active hydrogen containing groups of which more than 50% are primary active hydrogen containing groups and wherein the olamine has at least one phosphonic ester group attached to a tertiary nitrogen atom and contains at least two hydroxyl groups. The invention further relates to a flame-resistant polymer-modified polyol obtainable with the process of the invention, to a process for preparing optionally foamed plastics using the polymer-modified polyol of the invention, and to the use of a polymer-modified polyol for the preparation of flexible polyurethane foams.

Claims

1. A method for preparing a flame-resistant polymer-modified polyol dispersion having a solid content from 1 to 65 wt % based on the total weight of the dispersion comprising: reacting at least one polyisocyanate and an olamine in the presence of a base polyol having at least two active hydrogen containing groups of which more than 50% are primary active hydrogen containing groups, and a cross-linking agent having a weight average molecular weight from 500 to 800 g/mol, wherein the olamine has at least one phosphonic ester group attached to a tertiary nitrogen atom and has at least two hydroxyl groups; and wherein the ratio of NCO:OH equivalents between the NCO groups of the at least one polyisocyanate and the at least two hydroxyl groups of the olamine is in the range from 0.5:1 to 1.5:1.

2. The method according to claim 1, wherein the base polyol has a molecular weight from 2000 g/mol to 15000 g/mol.

3. The method according to claim 2, wherein the base polyol has 2-8 hydroxyl groups.

4. The method according to claim 1, wherein the base polyol is a polyether polyol wherein greater than 50% of the hydroxyl groups of the polyether polyol are primary hydroxyl groups.

5. The method according to claim 1, wherein the base polyol is a polyether polyol wherein up to 85% of the hydroxyl groups of the polyether polyol are primary hydroxyl groups.

6. The method according to claim 1, wherein the at least one polyisocyanate is in an isocyanate mixture, and wherein the isocyanate mixture further comprises up to 40 mol % of a monoisocyanate.

7. The method according to claim 1, wherein the ratio of NCO:OH equivalents between the NCO groups of the at least one polyisocyanate and the at least two hydroxyl groups of the olamine is in the range from 0.85:1 to 1.2:1.

8. The method according to claim 7, wherein the ratio of NCO:OH equivalents between the NCO groups of the at least one polyisocyanate and the at least two hydroxyl groups of the olamine is in the range from 0.9:1 to 1.15:1.

9. The method according to claim 1, wherein the olamine has the structural formula (I) ##STR00004## wherein each R.sup.1 and R.sup.2 are independently an alkyl group having 1-18 carbon atoms; each R.sup.3 and R.sup.4 are independently hydrogen atoms or hydrocarbon groups; each A.sup.1 and A.sup.3 are independently selected from ##STR00005## wherein m is an integer from 1 to 10; A.sup.2 is A.sup.1, an alkylene or aralylene group having 2 to 12 carbon atoms, or an arylene group; and n is an integer from 1 to 10.

10. The method according to claim 1, wherein the olamine has the structural formula (II) ##STR00006## wherein R.sup.1 and R.sup.2 are each independently an alkyl group having 1-18 carbon atoms, aryl, or aralkyl.

11. The method according to claim 1, wherein the cross linking agent has a functionality of 2 to 8 active hydrogen containing groups capable of reacting with isocyanate functions.

12. The method according to claim 11, wherein the cross linking agent has hydroxyl functions.

13. The method according to claim 1, wherein the cross linking agent is a polyether polyol.

14. The method according to claim 1, wherein the amount of cross linking agent present in the reacting step is from 0.1 to 11 g per 100 g of the flame-resistant polymer-modified polyol dispersion.

15. The method according to claim 1, wherein said reacting is performed in the presence of water; low molecular weight hydroxyl or amino containing compounds; catalysts; flame retardants; organic or inorganic fillers; synergists; or any combination thereof.

16. The method according to claim 1, wherein said reacting is performed at a temperature of 30° C. to 170° C.

17. The method according to claim 1, wherein said reacting is performed in a continuous manner.

18. A polymer-modified polyol dispersion generated according to the method of claim 1.

19. A method for preparing flame-resistant, optionally foamed polyurethane plastics, wherein at least one polyisocyanate is reacted with the polymer-modified polyol dispersion according to claim 18, optionally in the presence of water and/or volatile organic substances as blowing agents; catalysts; foaming auxiliaries and additives; chain-extending and/or crosslinking agents; organic or inorganic filling materials; flame retardants and/or synergists.

20. A method for preparing a flexible polyurethane foam comprising providing the polymer-modified polyol dispersion according to claim 18 and processing this polymer-modified polyol into a flexible polyurethane foam.

Description

DETAILED DESCRIPTION OF THE INVENTION

(1) To prepare a flame-resistant polymer-modified polyol of the present invention, (i) at least one polyisocyanate and (ii) an olamine are reacted in (iii) a base polyol having at least two active hydrogen containing groups of which more than 50% are primary active hydrogen containing groups in a manner similar to the preparation of the known PIPA polyol dispersions. According to the invention, the olamine has at least one phosphonic ester group attached to a tertiary nitrogen atom and contains at least two hydroxyl groups.

(2) The reaction is preferably carried out at a temperature of 30° C. to 170° C.

(3) The polymer-modified polyol dispersion thus obtained has a solids content of 1 to 65 wt. %, preferably of 2 to 50 wt. %, as polymer fraction.

(4) A polyol dispersion having a solids content of 3 to 25 wt. % is particularly preferable and of 5 to 15 wt. % is very particularly preferable. The solid content is preferably based on the total weight of the dispersion. The solid content can be in the form of polyurethane particles, in particular in the form of PIPA particles. The weight of the polyurethane particles, in particular of the PIPA particles, may be a calculated weight determined according to methods known in the art.

(5) The solid content (in wt. %) of the polymer-modified polyol may be calculated by dividing the sum of amounts (wt.) of olamines (including phosphorous-containing olamines, if any), polyisocyanates, and, if present, crosslinking agents, and, if present, other isocyanates (including, but not limited to, e.g. monoisocyanates), by the total amount (wt.) of starting materials and multiplying the result with 100.

(6) The phosphorus-containing olamine used according to the invention may be a polyhydroxy compound as described for example in DE 11 43 022 B. These compounds are obtainable by condensation of hydroxyl-containing primary or secondary aliphatic, cycloaliphatic, aromatic, araliphatic or heterocyclic mono- and/or polyamines with carbonyl compounds and dialkyl phosphites with or without subsequent oxyalkylation.

(7) The phosphorus-containing olamine preferably conforms to the following general formula (I):

(8) ##STR00001##

(9) where R.sup.1 and R.sup.2 are each independently an alkyl moiety of 1 to 18 carbon atoms, R.sup.3 and R.sup.4 are hydrogen atoms or any desired hydrocarbon moieties and A.sup.1 and also A.sup.3 are identical or different moieties of the formulae

(10) ##STR00002##

(11) where m is an integer from 1 to 10, and

(12) A.sup.2 is an alkylene or aralkylene moiety of 2 to 12 carbon atoms, an arylene moiety or an A.sup.1 or A.sup.3 moiety, and

(13) n is an integer from 0 to 10.

(14) It is particularly preferable for the phosphorus-containing olamine to conform to the following general formula (II):

(15) ##STR00003##

(16) where R.sup.1 and R.sup.2 are the same or different and are each independently alkyl of 1 to 18 carbon atoms, preferably 1 to 4 carbon atoms, aryl or aralkyl.

(17) Very particularly preferred is diethyl N,N-bis(hydroxyethyl)aminomethylphosphonate; (CAS: 2781-11-5), which is marketed by PCC-Rokita under the name Roflam® 6.

(18) The phosphorus-containing olamine used according to the invention may be present in the reaction mixture in an amount of from 1 to 25 g/100 g flame-resistant polymer-modified polyol, preferably from 3 to 22 g/100 g flame-resistant polymer-modified polyol, more preferably from 5 to 20 g/100 g flame-resistant polymer-modified polyol, even more preferably from 7 to 17 g/100 g flame-resistant polymer-modified polyol.

(19) The reaction with the phosphorus-containing olamines (ii) and the base polyol components (iii) to obtain the polyol dispersions of the present invention and the conversion thereof into polyurethane plastics may utilize not only monoisocyanates, such as phenyl isocyanate or stearyl isocyanate, but also aliphatic, cycloaliphatic, araliphatic, aromatic and heterocyclic polyisocyanates having at least two NCO groups, described for example by W. Siefken in Justus Liebigs Annalen der Chemie, 562 (1949), pages 75-136.

(20) Useful polyisocyanates include, for example, ethylene diisocyanate, 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, 1,12-dodecane diisocyanate, cyclobutane 1,3-diisocyanate, cyclohexane 1,3-diisocyanate, cyclohexane 1,4-diisocyanate and also any desired mixtures of these isomers, 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethylcyclohexane, 2,4- and/or 2,6-hexahydrotolylene diisocyanate and also any desired mixtures of these isomers, hexahydro-1,3- and/or -1,4-phenylene diisocyanate, perhydro-2,4′- and/or -4,4′-diphenylmethane diisocyanate, 1,3- and/or 1,4-phenylene diisocyanate, 2,4- and/or 2,6-tolylene diisocyanate and also any desired mixtures of these isomers, diphenylmethane 2,4′- and/or 4,4′-diisocyanate, naphthylene 1,5-diisocyanate, triphenylmethane 4,4′,4″-triisocyanate.

(21) Suitable polyisocyanates further include polyphenyl polymethylene polyisocyanates of the type obtainable by aniline-formaldehyde condensation and subsequent phosgenation.

(22) Further examples are polyisocyanates comprising carbodiimide groups, polyisocyanates comprising allophanate groups, polyisocyanates comprising urethane groups, polyisocyanates comprising acylated urea groups, polyisocyanates comprising biuret groups, polyisocyanates obtained by telomerisation reactions, polyisocyanates comprising ester groups and reaction products of the abovementioned isocyanates with acetals.

(23) Suitable diisocyanates include not only aliphatic diisocyanates, such as hexamethylene diisocyanate and tetramethylene diisocyanate, but also cycloaliphatic diisocyanates such as, for example, hexahydro-p-phenylene diisocyanate, and especially aromatic diisocyanates such as, for example, tolylene diisocyanate, 4,4′-diphenylmethane diisocyanate, 1,5-naphthylene diisocyanate and p-phenylene diisocyanate.

(24) Particular preference is generally given to the industrially readily accessible polyisocyanates such as 2,4- and/or 2,6-tolylene diisocyanate and any desired mixtures of these isomers (“TDI”), polyphenyl polymethylene polyisocyanates of the type obtainable by aniline-formaldehyde condensation and subsequent phosgenation (“crude MDI”) and polyisocyanates comprising carbodiimide groups, urethane groups, allophanate groups, isocyanurate groups, urea groups or biuret groups (“modified polyisocyanates”).

(25) The polyisocyanate may be used singly or in admixture with other polyisocyanates. The polyisocyanate may further be in a mixture with up to 40 mol % of a monoisocyanate.

(26) The polyisocyanate used according to the invention may be present in the reaction mixture in an amount of from 1 to 20 g/100 g flame-resistant polymer-modified polyol, preferably from 2 to 18 g/100 g flame-resistant polymer-modified polyol, more preferably from 3 to 15 g/100 g flame-resistant polymer-modified polyol, even more preferably from 4 to 14 g/100 g flame-resistant polymer-modified polyol.

(27) The equivalents ratio NCO:OH between the OH groups of the phosphorus-containing olamine (ii) and the NCO groups of the at least one polyisocyanate (i) and also optionally of the monoisocyanate is preferably in the range from 0.5 to 1.5.

(28) The equivalents ratio NCO:OH is more preferably in the range from 0.85 to 1.2 and even more preferably in the range from 0.9 to 1.15.

(29) The base polyol (iii) used for preparing the polymer-modified polyol dispersion of the present invention has at least two active hydrogen containing groups of which more than 50% are primary active hydrogen containing groups and preferably a weight average molecular weight Mw in the range from 2000 g/mol to 15000 g/mol.

(30) The weight average molecular weight Mw of the base polyol is more preferably in the range from 2500 to 12000 and yet more preferably in the range from 3000 to 7000 g/mol.

(31) It is particularly preferable for the base polyol to be a polyether polyol (poly(oxyalkylene) polyol) having an OH functionality in the range from 2 to 8 and a weight average molecular weight of Mw=2000 to 15 000 g/mol.

(32) If desired, mixtures of two or more polyols are also usable as base polyol.

(33) The base polyol may be in the form of a homopolymer, a copolymer or block copolymer.

(34) The poly(oxyalkylene) polyols used with preference are commercially available or are obtainable in a conventional manner by polyaddition of alkylene oxides such as ethylene oxide, propylene oxide, butylene oxide and styrene oxide, optionally mixed or in succession onto polyfunctional starting compounds. The choice of alkylene oxide can influence the presence of primary or secondary hydroxyl groups in the resulting polyether polyol as is known in the art.

(35) Examples of preferred starter compounds are water, alcohols or amines but especially molecules having two to six primary or secondary amine groups or hydroxyl groups per molecule such as triethanolamine, 1,2-ethanediol, 1,2-propanediol, 1,3-propanediol, diethylene glycol, dipropylene glycol, triethylene glycol, tripropylene glycol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 1,2-hexanediol, 1,4-hexanediol, 1,5-hexanediol, 1,6-hexanediol, glycerol, trimethylolpropane, pentaerythritol, mannitol or sorbitol, 4,4′-dihydroxy-diphenylpropane, aniline, mono- and diethanolamine, ethylenediamine and diethylenetriamine. Sucrose polyethers and also formitol- or formose-started polyethers also come into consideration for the purposes of the present invention. The choice of starter molecule can influence the functionality of the resulting polyether polyol as is known in the art.

(36) For the base polyol, particular preference is given to such polyethers where the predominant proportion, preferably more than 50%, more preferably more than 70%, even more preferably up to 85%, of all the OH groups present in the polyether are primary OH groups. Polybutadienes comprising OH groups or hydroxyl-functional polymers of tetrahydrofuran are also suitable for the purposes of the present invention.

(37) Suitable base polyols for the applications in flexible foams preferably have a hydroxyl number of 20 to 100 mg/KOH and/or a dynamic viscosity in the range from 400 to 6000 mPa.Math.s.

(38) The base polyol used according to the invention may be present in the reaction mixture in an amount from 35 to 99 g/100 g flame-resistant polymer-modified polyol, preferably from 50 to 95 g/100 g flame-resistant polymer-modified polyol, more preferably from 60 to 95 g/100 g flame-resistant polymer-modified polyol, even more preferably from 65 to 90 g/100 g flame-resistant polymer-modified polyol.

(39) According to an embodiment of the invention, the reaction is carried out in the presence of a cross-linking agent having a weight average molecular weight from 200 to 1000 g/mol. Conducting the reaction in the presence of a cross-linking agent with a weight average molecular weight in the above range can help to obtain polymer-modified polyols that yield flexible foams with improved mechanical properties. Without wishing to be bound by theory, it is believed that the use of a cross-linking agent as described herein improves the miscibility and/or the compatibility in the resulting polymer-modified polyol.

(40) Preferably, the cross-linking agent may have a weight average molecular weight from 400 to 900 g/mol and more preferably from 500 to 800 g/mol.

(41) According to another embodiment of the invention, the cross-linking agent has a functionality of 2 to 8, in particular 3 to 6, active hydrogen containing groups, capable of reacting with isocyanate functions. It has been found that a functionality of the cross-linking agent in this range yields a polymer-modified polyol that can be used to prepare flexible foams with good mechanical properties.

(42) The functionality can in particular mean the number of functional groups, in particular the number of a specific functional group, in a molecule. For example, a cross-linking agent with a functionality of 2 to 8 active hydrogen containing groups can be a cross-linking agent in which each molecule of the cross-linking agent has 2 to 8 active hydrogen containing groups.

(43) According to another embodiment of the invention, the cross-linking agent contains hydroxyl functions. Cross-linking agents with hydroxyl groups have been found to yield polymer-modified polyols with very good properties for flexible foams.

(44) According to another embodiment of the invention, the cross-linking agent is a polyether polyol. Polyether polyol cross-linking agents have been found to be particularly beneficial for the compatibility and the miscibility of the resulting polymer-modified polyol.

(45) Advantageously, the cross-linking agent, when used, is present in the reaction in an amount of from 0.1 to 11 g/100 g flame-resistant polymer-modified polyol, in particular from 0.2 to 7 g/100 g flame-resistant polymer-modified polyol, more particularly from 0.5 to 6 g/100 g flame-resistant polymer-modified polyol. Practical experiments have shown that the use of more than substantially 11 g cross-linking agent per 100 g flame-resistant polymer-modified polyol resulted in polymer-modified polyols that yielded foams with bad properties, in particular a bad resilience and a high rigidity. On the other hand, it has been found that the use of less than 0.1 g cross-linking agent per 100 g flame-resistant polymer-modified polyol did not have any effect on the properties of foams prepared from the resulting flame-resistant polymer-modified polyols.

(46) The details mentioned above for the preparation, the functionality, and/or the type of hydroxyl groups (that is, primary or secondary hydroxyl groups) of the base polyol preferably also apply for the cross-linking agent.

(47) The reaction of the polyisocyanate (i) with the phosphorus-containing olamine (ii) in the base polyol (iii) may be carried out in the presence of water at not more than 0.25 wt. % and/or low molecular weight hydroxyl- or amino-containing compounds having a molecular weight of below 400 g/mol at not more than 5 wt. % and/or catalysts and/or further flame retardants and/or synergists, and/or organic and inorganic fillers and/or further auxiliaries.

(48) By way of low molecular weight hydroxy compounds there may be used ethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, 1,4-butylene glycol, 2,3-butylene glycol, 1,6-hexanediol, 1,8-octanediol, neopentyl glycol, 1,4-bis-hydroxymethylcyclohexane, 2-methyl-1,3-propanediol, glycerol, trimethylolpropane, 1,2,6-hexanetriol, 1,2,4-butanetriol, trimethylolpropane, pentaerythritol, quinitol, mannitol and sorbitol, formitol, methylglycoside, diethylene glycol, triethylene glycol, tetraethylene glycol and higher polyethylene glycols, dipropylene glycol and higher polypropylene glycols and also dibutylene glycol and higher polybutylene glycols at a maximum molecular weight of 400 g/mol.

(49) Examples of suitable low molecular weight amines are ethylenediamine, diethylenetriamine, N,N-dimethylethylenediamine, piperazine, 4-aminobenzylamine, 4-aminophenylethylamine, o-, m- and p-phenylenediamine, 2,4- and/or 2,6-tolylenediamine, 4,4′-diaminodiphenylmethane and/or olamines such as ethanolamine, di- and triethanolamine, propanolamine, di- and tripropanolamine, butanolamine and di- and tributanolamine.

(50) Suitable catalysts are organometallic compounds such as dibutyltin oxide and dibutyltin dichloride and/or catalysts based on Sn(+II), Sn(+IV), Bi(+III), Zn(+II) or Zr(+IV) salts of carboxylic acids such as tin(II) acetate, tin(II) octoate, tin(II) ethylhexoate, tin(II) laurate, tin(II) palmitate, tin(II) stearate, tin(II) oleate, dibutyltin diacetate, dibutyltin dilaurate, dibutyltin maleate, dioctyltin diacetate, bismuth(III) neodecanoate, zinc(II) octoate, zinc(II) ricinoleate, zinc(II) neodecanoate and zirconium(IV) ethylhexoate.

(51) The catalyst used according to the invention may be present in the reaction mixture in an amount of from 0.01 to 1.5 g/100 g flame-resistant polymer-modified polyol, preferably from 0.03 to 1 g/100 g flame-resistant polymer-modified polyol, more preferably from 0.05 to 0.5 g/100 g flame-resistant polymer-modified polyol, even more preferably from 0.08 to 0.2 g/100 g flame-resistant polymer-modified polyol.

(52) As supplementary, preferably halogen-free flame retardants there may be used phosphorus compounds such as tert-butylphenyl diphenyl phosphate, isopropylphenyl diphenyl phosphate, tricresyl phosphate and dimethyl methanephosphonate and/or nitrogen compounds such as melamine, in each case alone or combined with further synergists such as zinc borate, and zinc stannate.

(53) It is additionally possible to use known organic and/or inorganic filling materials such as CaCO.sub.3 and also further auxiliaries such as emulsifiers, colour pastes and stabilizers.

(54) The process which the present invention provides for preparing the polymer-modified polyol by reacting the at least one polyisocyanate (i) with the phosphorus-containing olamines (ii), which have phosphonic ester groups attached to tertiary nitrogen atoms and at least two hydroxyl groups, in base polyol (iii) may be carried out in a batch operation or in a continuous operation.

(55) In the batch operation, the base polyol may be initially charged together with the phosphorus-containing olamine at temperatures between 10° C. and 100° C. and the polyisocyanate added. It is also possible to initially charge the base polyol only and to add the phosphorus-containing olamine and also the polyisocyanates into the base polyol in synchronous fashion, in which case the heat of reaction is optionally removed by cooling in both scenarios.

(56) However, a continuous or semi-continuous procedure is advantageous where the mixing of the polyisocyanate with the phosphorus-containing olamine and the polyether polyols is effected synchronously, for example in a fast-rotating mixing head, and the more or less converted reaction mixture, depending on the average residence time in the mixing head, is transferred into a stirred tank or agitated stock reservoir tank for further reaction. In this form of reaction management, the reaction mixture may also undergo subsequent reaction in two or more stirred tanks serially connected in the form of a cascade, at temperatures between 50° C.-150° C., in which case the heat of reaction is optionally removed by cooling in either scenario.

(57) It is preferable to maintain an equivalents ratio of NCO:OH groups between 0.85 and 1.20, yet more preferably between 0.95 and 1.10.

(58) The concentration of the solid polyaddition products in the polyether polyols may be adjusted to values between 1 and 65 wt. % in the final polyol dispersion. However, preference is given to a solids content between 3 and 25 wt. %, very particularly between 5 and 15 wt. %.

(59) The polymer-modified polyols according to the invention can also be prepared using a seeding process. When using a seeding process, a polymer-modified polyol with a low solid content, for example from 0.01 to 5 wt. %, based on the amount of polymer-modified polyol, is used as the base polyol and further polyisocyanate as well as olamine and optionally cross-linking agent and optionally catalyst are added. In this mixture, the solid content already present in the mixture in the form of polymer particles act as nuclei that grow as the reaction proceeds. In this way, the solid content can be easily adjusted to the desired value. Further, it is also possible to conduct an “in situ seeding”, wherein a first amount of the polyisocyanate is added to the mixture of base polyol and optionally a catalyst followed by addition of the olamine with at least one phosphonic ester group attached to a tertiary nitrogen atom and at least two hydroxyl groups, in a second step. The reaction can then be allowed to react before in a third step, a second amount of polyisocyanate is added. Using either of the seeding processes, bimodal particle distributions can be obtained. This can help to tailor the properties of the resulting plastics, in particular the foams.

(60) The amount of dispersed polyaddition product required for foams to have optimum physicomechanical as well as flame-retardant properties is from 5 to 15 wt. %. It will be appreciated that such dispersions of low solids content are obtainable directly according to the present invention. However, a multi-step procedure is preferred where a dispersion having a high solids content between 25 and 65 wt. % is prepared in the first step and is then adjusted to the desired solids concentration with any desired polyol, for example the polyether polyol already used in the first step, some other of the polyether polyols mentioned above, a polyester polyol, a further polyol dispersion such as, for example, a further polyisocyanate polyaddition polyol dispersion (PIPA) prepared with an olamine in a conventional manner and/or a styrene-acrylonitrile polyether dispersion (SAN-PE) and/or polyurea dispersion (PUD) or mixtures of all the polyols referred to here. This is a simple way to expand the property profiles of the polymer-modified polyol dispersions of the present invention.

(61) The polymer-modified polyol dispersions of the present invention are advantageously processible into flexible polyurethane foams having improved properties, such as enhanced tensile strength and hardness. The dispersions are likewise useful for producing elastomers, coatings and overcoatings. To this end, the polymer-modified polyol dispersions of the present invention are reacted, optionally in the presence of other customary polyols, with aliphatic, cycloaliphatic, araliphatic, aromatic and heterocyclic polyisocyanates, optionally in the presence of known auxiliaries and additives.

(62) Known auxiliaries and additives are, in particular, water and/or volatile organic substances as blowing agents which may optionally be used together with catalysts, foaming auxiliaries and additives, chain-extending and/or crosslinking agents, organic or inorganic filling materials, flame retardants and/or synergists.

(63) This provides flame-resistant, optionally foamed polyurethane plastics, in particular flexible foams, having good mechanical and physical properties, thermal and hydrolytic stability and no components with a tendency to migrate.

EXAMPLES

(64) I) Flame Resistant (FR) Polyol Synthesis

(65) Apparatuses Used:

(66) TABLE-US-00001 T 50 ULTRA-TURRAX ® High-performance dispersing instrument. Hennecke Labfoam ® Semi continuous operating laboratory plant for test series and laboratory purposes.

(67) Chemicals Used:

(68) TABLE-US-00002 Polyol A Glycerin started polyoxypropylene polyol capped with ethylene oxide with a functionality of approximately 3, and LOH of 33-38 mg KOH/g and a weight average molecular weight of Mw = 4800 g/mol. Polyol B Reactive polymer modified polyol with a solid content of 10%, a functionality of approximately 3, and LOH of 47-52 mg KOH/g and a weight average molecular weight of Mw = 4850 g/mol. Polyol C Reactive polymer modified polyol with a solid content of 20%, a functionality of approximately 3, and LOH of 50-57 mg KOH/g and a weight average molecular weight of Mw = 4850 g/mol. Polyol D Reactive styrene-acrylonitrile copolymer modified polyol with a solid content of 40%, a functionality of approximate 3, and LOH of 20-23 mgKOH/g and a weight average molecular weight of Mw = 4800 g/mol. Polyol E Polyoxyalkylene triol with a weight average molecular weight of Mw = 3000 g/mol and an LOH of 53-59 mg KOH/g. Crosslinker A Sorbitol started polyoxyalkylene polyol with a LOH of 400-440 mg KOH/g and a weight average molecular weight of Mw = 600. FR olamine Diethyl N,N-bis(hydroxyethyl)aminomethyl- phosphonate (CAS: 2781-11-5); with a functionality of approximately 2, and LOH of app. 450 mg KOH/g Triethanolamine Tris(2-hydroxyethyl)amine (CAS: 102-71-6) (TEA) Ongronat ®1080 Toluenediisocyanate (TDI) - mixture consisting of 80 wt. % 2,4-und 20 wt. % 2,6-isomer (CAS 584-84-9) Kosmos ® 19 Gelling catalyst (Dibutyltindilaurate (DBTDL), Evonik) Kosmos ® 54 Gelling catalyst (Zinc ricinoleate, Evonik) Bicat 4130M Gelling catalyst (Zirconium neodecanoat mixture, Shepherd) Bicat ZM Gelling catalyst (Zinc dineodecanoate, Shepherd).

(69) Chemical Physical Properties of the Polyols Listed were Determined in Accordance with Following Standards, Internal Audit Procedures and Measurement Methods:

(70) TABLE-US-00003 TABLE 1 Water Content in wt. % DIN 51777 Hydroxyl Number (LOH) in mg KOH/g DIN 53240 Acid Number in mg KOH/g DIN EN ISO 3682 Dynamic Viscosity (25° C.) in mPa .Math. s DIN 51 550 Color (Pt/Co) in Hazen DIN ISO 6271

(71) The solid content (in wt. %) of the polymer-modified polyol was calculated by dividing the sum of amounts (wt.) of olamines (including phosphorous-containing olamines, if any), organic polyisocyanates, and, if present, crosslinking agents, and, if present, other isocyanates (including, but not limited to, e.g. monoisocyanates), by the total amount (wt.) of starting materials and multiplying the result with 100.

Example No. 1-11

(72) General Procedure for Manufacturing of 10 kg FR-Polyol:

(73) The base polyol is transferred together with the FR olamine and the gelling catalyst in a dried 15l glass reactor, equipped with a stirrer, a dispersing device (Ultraturrax T50), a thermometer and a dropping funnel. After exclusion of air and moisture by purging with nitrogen, the reaction mass is thoroughly mixed for 10 minutes whereby the temperature increases to 35-45° C.

(74) Then the Ongronat® 1080 is added slowly during a period 30 minutes and the temperature rises to 55-75° C. while the reaction mixture starts immediately to whiten. The resulting polyol dispersion is then slowly stirred for another two hours and finally stored for 24 hours with exclusion of air and moisture.

Example No. 1a-1d

(75) FR-Polyols with Different Molar Ratios (equivalents ratios) NCO:OH

(76) TABLE-US-00004 TABLE 2 Example No. 1a 1b 1c 1d Polyol A [g] 8419.71 8352.71 8285.72 8218.72 Fr olamine [g] 1000.00 1000.00 1000.00 1000.00 Kosmos ® 19 [g] 10.84 10.84 10.84 10.84 Ongronat ®1080 [g] 569.45 636.45 703.44 770.44 Molar Ratio NCO:OH 0.85 0.95 1.05 1.15 T50 mixing [rpm] 5000 5000 5000 5000 Solid Content [wt. %] 15.7 16.4 17.0 17.7 P - Content [wt. %] 1.21 1.21 1.21 1.21 N - Content [wt. %] 1.54 1.65 1.75 1.86 Dynamic Viscosity [mPa .Math. s] 2097 2774 3786 9436 LOH [mgKOH/g] 36.6 34.8 30.4 25.6

Example No. 2a-2d

(77) FR Polyols with Different Solid Contents:

(78) TABLE-US-00005 TABLE 3 Example No. 2a 2b 2c 2d Polyol A [g] 8806.13 8299.12 7623.10 7285.09 FR olamine [g] 700.00 1000.00 1400.00 1600.00 Kosmos ® 19 [g] 10.84 10.84 10.84 10.84 Ongronat ®1080 [g] 483.03 690.04 966.06 1104.07 Molar Ratio NCO:OH 1.03 1.03 1.03 1.03 T50 mixing [rpm] 5000 5000 5000 5000 Solid Content [wt. %] 11.8 16.9 23.7 27.0 P - Content [wt. %] 0.85 1.21 1.70 1.94 N - Content [wt. %] 1.21 1.73 2.43 2.77 Dynamic Viscosity [mPa .Math. s] 2795 3341 5225 6563 LOH [mgKOH/g] 32.8 30.7 30.4 28.5

Example No. 3a-3d FR Polyols, Prepared with Different Gelling Catalysts

(79) TABLE-US-00006 TABLE 4 Example No. 3a 3b 3c 3d Polyol A [g] 8489.12 8489.12 8489.12 8489.12 FR olamine [g] 887.57 887.57 887.57 887.57 Kosmos ® 19 [g] 10.84 0.00 0.00 0.00 Kosmos ® 54 [g] 0.00 10.84 0.00 0.00 Bicat ® 4130 M [g] 0.00 0.00 10.84 0.00 Bicat ® ZM [g] 0.00 0.00 0.00 10.84 Ongronat ®1080 [g] 612.47 612.47 612.47 612.47 Molar Ratio NCO:OH 1.03 1.03 1.03 1.03 T50 mixing [rpm] 5000 5000 5000 5000 Solid Content [wt. %] 15.0 15.0 15.0 15.0 P - Content [wt. %] 1.08 1.08 1.08 1.08 N - Content [wt. %] 1.54 1.54 1.54 1.54 Dyn. Viscosity [mPa .Math. s] 3065 4652 5225 3057 LOH [mgKOH/g] 32.8 30.7 30.4 34.3

(80) The Zn(II)neodecanoate catalyst Bicat® ZM exhibits comparable performance regarding viscosity and stability of the resulting dispersions to the DBTDL catalyst Kosmos® 19.

Example No. 4a-5c

(81) General Procedure for Manufacturing of 10 kg FR-Polyol with In Situ Seeding (TEA):

(82) The base polyol is transferred together with the olamine (TEA) and the gelling catalyst in a dried 15 l glass reactor, equipped with a stirrer, a dispersing device (Ultraturrax T50), a thermometer and a dropping funnel. After exclusion of air and moisture by purging with nitrogen, the reaction mass is thoroughly mixed for 10 minutes whereby the temperature increases to 35-45° C.

(83) Then the first amount of Ongronat® 1080 is added slowly during a period of 10 minutes. The reaction mixture is thoroughly mixed for 10 minutes, then the FR olamine is added and mixing proceeds for another 10 minutes. The remaining amount of Ongronat® 1080 is added slowly during a period of 10 minutes and the temperature rises to 55-75° C. while the reaction mixture starts immediately to whiten. The resulting polyol dispersion is then slowly stirred for another two hours and finally stored for 24 hours with exclusion of air and moisture.

(84) TABLE-US-00007 TABLE 5 Example No. 4a 4b 4c 5a 5b 5c Polyol A [g] 8796.12 8289.10 7275.08 8786.10 8279.09 7265.06 Triethanolamin [g] 3.57 3.57 3.57 7.14 7.14 7.14 Ongronat ®1080 1st [g] 6.44 6.44 6.44 12.88 12.88 12.88 FR olamine [g] 700.00 1000.00 1600.00 700.00 1000.00 1600.00 Ongronat ®1080 2nd [g] 483.03 690.04 1104.07 483.03 690.04 1104.07 Kosmos ® 19 [g] 10.84 10.84 10.84 10.84 10.84 10.84 Molar Ratio NCO:OH 1.03 1.03 1.03 1.03 1.03 1.03 T50 mixing [rpm] 5000 5000 5000 5000 5000 5000 Solid Content [wt. %] 11.9 17.0 27.1 12.0 17.1 27.2 P - Content [wt. %] 0.85 1.21 1.94 0.85 1.21 1.94 N - Content [wt. %] 1.21 1.73 2.77 1.21 1.73 2.77 Dynamic Viscosity [mPa .Math. s] 2795 3341 6563 2648 3522 4945 LOH [mgKOH/g] 32.8 30.7 28.5 31.9 32.6 29.4

Example No. 6a-7c

(85) General Procedure for Manufacturing of 10 kg FR-Polyol with Seeding:

(86) The polyol components consisting of the base polyol and the seeding polyol are transferred together with the FR olamine and the gelling catalyst in a dried 15 l glass reactor, equipped with a stirrer, a dispersing device (Ultraturrax T50), a thermometer and a dropping funnel. After exclusion of air and moisture by purging with nitrogen, the reaction mass is thoroughly mixed for 10 minutes whereby the temperature increases to 35-45° C. Then the Ongronat® 1080 is added slowly during a period 30 minutes and the temperature rises to 55-75° C. while the reaction mixture starts immediately to whiten. The resulting polyol dispersion is then slowly stirred for another two hours and finally stored for 24 hours with exclusion of air and moisture.

(87) TABLE-US-00008 TABLE 6 Example No. 6a 6b 6c 7a 7b 7c Polyol A [g] 7291.79 7191.79 7091.79 8176.75 8076.75 7976.75 Polyol B [g] 100.00 200.00 300.00 100.00 200.00 300.00 FR olamine [g] 1600.00 1600.00 1600.00 1000.00 1000.00 1000.00 Ongronat ® 1080 [g] 997.37 997.37 997.37 712.41 712.41 712.41 Kosmos ® 19 [g] 10.84 10.84 10.84 10.84 10.84 10.84 Molar Ratio NCO:OH 1.03 1.03 1.03 1.03 1.03 1.03 T50 mixing [rpm] 5000 5000 5000 5000 5000 5000 Solid Content [wt. %] 26.07 26.17 26.27 17.22 17.32 17.42 P - Content [wt. %] 1.93 1.93 1.93 1.93 1.93 1.93 N - Content [wt. %] 2.37 2.37 2.37 2.37 2.37 2.37 Dynamic Viscosity [mPa .Math. s] 5675 4587 4997 2950 3602 3381 LOH [mgKOH/g] 33.70 34.20 32.90 35.40 33.90 31.20

Example No. 8-11

(88) Discontinuous Preparation of FR Polyol with a High Solid Content in Terms of a Master Batch and Subsequent Dilution with Different Polymer Modified and Standard Poylols:

(89) First, a FR Polyol with a final solid content of 27% and containing 16% FR olamine is prepared according to the general procedure without seeding described above. This FR polyol is then blended before the final 24 hour storage, with a second polyol and intensely mixed for 10 minutes. The resulting polyol dispersion is then slowly stirred for another two hours and finally stored for 24 hours with exclusion of air and moisture.

(90) TABLE-US-00009 TABLE 7 Example No. 8 9 10 11 12 Polyol A [g] 6223.79 6223.79 6223.79 6223.79 5169.30 Polyol B [g] 62.50 62.50 62.50 62.50 43.75 FR olamine [g] 1000.00 1000.00 1000.00 1000.00 700.00 Ongronat ® 1080 [g] 623.75 623.75 623.75 623.75 436.63 Kosmos ® 19 [g] 6.78 6.78 6.78 6.78 4.74 Polyols used for blending Polyol A [g] 2083.19 0.00 0.00 0.00 0.00 Polyol B [g] 0.00 2083.19 0.00 0.00 0.00 Polyol C [g] 0.00 0.00 2083.19 0.00 0.00 Polyol D [g] 0.00 0.00 0.00 2083.19 0.00 Polyol E [g] 0.00 0.00 0.00 0.00 3645.58 Molar Ratio NCO:OH 1.03 1.03 1.03 1.03 1.03 T50 mixing [rpm] 5000.00 5000.00 5000.00 5000.00 5000.00 Solid Content [wt. %] 16.30 18.38 20.47 24.63 11.41 Dynamic Viscosity 2847 3226 3845 4775 5631 [mPa .Math. s] LOH [mgKOH/g] 39.90 44.20 41.70 45.40 39.50

Example No. 13a-c

(91) Continuous Preparation of FR Polyol, also in the Presence of a Crosslinker:

(92) Polyol A, Polyol B, the crosslinking agent, and FR olamine are fed simultaneously via a mixing head together with the gelling catalyst at ambient temperature to a post reaction vessel, equipped with a stirrer under exclusion of air and moisture under a nitrogen blanket, where the reaction mass is slowly stirred for further 48 hours with exclusion of air and moisture.

(93) TABLE-US-00010 TABLE 8 Example No. 13a 13b 13c Polyol A [kg/min] 80.47 69.69 78.49 Crosslinker A [kg/min] 0 0 1.89 Polyol B [kg/min] 1.64 1.42 1.64 FR olamine [kg/min] 10 16 10 Ongronat ® 1080 [kg/min] 6.2 10.18 7.37 Kosmos ® 19 [g/min] 67.6 108.4 67.6 Molar Ratio NCO:OH 0.95 0.95 0.95 Solid Content [wt. %] 19.5 30.3 22.6 Dynamic Viscosity [mPa .Math. s] 3912 9874 3553 LOH [mgKOH/g] 37.3 34.8 35

(94) II) Foam Preparation

(95) Apparatuses Used:

(96) TABLE-US-00011 Hennecke Semi continuous operating laboratory plant for Labfoam ® test series and laboratory purposes. Pendraulik ®31832 Laboratory mixer for application of high shear forces Foamat ® Foam rise height measurement testing device for determination of rise profiles Zwick Roell ®Z010 Static materials testing machines for determination of foam hardness, foam density and SAG factor

(97) Chemicals Used:

(98) TABLE-US-00012 Water Chemical blowing agent. DEOA 90% 90% solution of diethanolamine in water. ORTEGOL ® Crosslinker with a delayed reaction (Evonik). 204 B 8783 LF2 Surfactant - efficient HR silicone (Evonik). DABCO BLV Amine catalyst (Air products). Niax A1 Amine Catalyst (Momentive). KOSMOS ® 29 Gelling catalyst (stannous octoate, Evonik). Niax A300 Reactive amine catalyst (Momentive). Niax A400 Reactive amine catalyst (Momentive). Niax A-33 Amine catalyst (Momentive). Niax L-3002 Silicone Surfactant (Momentive). Ongronat ®1080 Toluenediisocyanate (TDI) - mixture consisting of 80% wt 2,4- and 20% wt 2,6-Isomer (CAS 584-84-9). Ongronat ® 2,2′/2,4′ and 4,4′-Methylene diphenyl diisocyanate. TR 4040 MDI is an aromatic isocyanate.

(99) Physical Mechanical Properties:

(100) The physical mechanical properties and the flame retardance of the foam samples listed were determined in accordance with the following standards, internal audit procedures and measurement methods:

(101) TABLE-US-00013 TABLE 9 Hardness in kPa DIN EN ISO 3386-1 Air Flow in L/sec DIN EN ISO 7231 Resilience in % DIN EN ISO 8307 SAG-Factor ASTM D-1564-64T Compression Set in % DIN EN ISO 1856 (22 h, 70° C., 50%) (CS dry, 50%) Cal 117 TECHNICAL BULLETIN 117-A FMVSS 302 EN ISO 3795 CRIB 5 BS 5852:2006 Crib ignition source 5

(102) General Procedure for Manufacturing of Flexible High Resilience Foams:

(103) All components except the gelling catalyst and the isocyanate are thoroughly mixed at 2800 rpm with the help of the Pendraulik dispergator in a 1 liter plastic bucket for 20 seconds.

(104) After addition of the gelling catalyst the reaction mixture is first stirred under the same conditions for another 10 seconds and then, after quick addition of the whole amount of Ongronat® 1080, the whole reaction mixture is mixed for another 7 seconds at 3500 rpm.

(105) The reaction mass is then quickly dropped into a paper box and the foam evolution is monitored via the Foamat® Apparatus.

Examples 15a-15g: Foams with Polyol A

(106) TABLE-US-00014 TABLE 10 Example No. 15a 15b 15c 15d 15e 15f 15g Ongronat ®1080 [g] 52.42 40.85 39.74 39.73 31.76 31.77 32.88 FR Polyol Ex. No. 4b [g] 100 100 — — 100 — — FR Polyol Ex. No. 7a [g] — — 100 — — 100 — FR Polyol Ex. No. 7b [g] — — — 100 — — 100 water add [g] 3.475 2.625 2.675 2.675 1.875 1.875 1.825 water total [g] 4 3.1 3.1 3.1 2.3 2.3 2.3 DABCO BLV [g] 0.1 0.15 0.15 0.15 0.18 0.18 0.18 DEOA 90% [g] 1.5 1 0.5 0.5 0.5 0.5 1 Ortegol ®204 [g] 1.5 1.5 1.5 1.5 1.5 1.5 1.5 B 8783 LF2 [g] 0.3 0.3 0.3 0.3 0.3 0.3 0.3 Kosmos ®29 [g] 0.15 0.15 0.15 0.13 0.15 0.18 0.18 Rise Time [sec] 90 108 114 118 138 128 123

(107) Foam Properties

(108) TABLE-US-00015 TABLE 11 Example No. 15g 15a 15b 15c 15d 15e 15f Density [kg/m3] 24.5 31.1 29.6 32.3 40.9 42.1 41.1 Hardness [kPa] 1.6 1.8 2.1 2 2.1 2.2 1.9 SAG 2.9 3 2.9 2.9 3.1 3.2 3.3 Airflow [L/sec] 1.04 1 0.4 0.53 0.9 0.95 1.07 CS dry 50, % 9.9 6.7 8.8 9.6 7.5 8.7 12.8 Resilience, % 52 55 47 47 54 53 53 Cal 117 Pass Pass Pass Pass Pass Pass Pass FMVSS SE/NBR SE SE SE DNI DNI DNI

Examples 16a-16i: Foams Without Melamine Part 1

(109) TABLE-US-00016 TABLE 12 Example No. 16a 16b 16c 16d 16e 16f 16g 16h 16i Ongronat ®1080 [g] 39.70 39.73 39.70 39.16 39.01 38.46 30.46 30.48 48.24 FR Polyol Ex. No. 6a [g] 100 100 — — — — 100 — 100 FR Polyol Ex. No. 6b [g] — — 100 100 — — — 100 — FR Polyol Ex. No. 6c [g] — — — — 100 100 — -— — water add [g] 2.65 2.65 2.65 2.675 2.78 2.8 2 2 3.425 water total [g] 3.1 3.1 3.1 3.1 3.1 3.1 2.3 2.3 3.9 DABCO BLV [g] 0.2 — — — — — — — — Niax A1 [g] — 0.2 0.2 0.2 0.2 0.2 0.2 0.25 0.15 DEOA 90% [g] 0.75 0.75 0.75 0.5 0.75 0.5 0.5 0.5 1 Ortegol ®204 [g] 1.5 1.5 1.5 1.5 1 1 1 1 1.5 B 8783 LF2 [g] 0.3 0.3 0.3 0.3 0.3 0.3 0.3 0.3 0.3 Kosmos ®29 [g] 0.1 0.15 0.1 0.12 0.12 0.12 0.12 0.12 0.1 Rise Time [sec] 140 100 114 112 120 120 150 130 100

(110) Foam Properties

(111) TABLE-US-00017 TABLE 13 Example No. 16a 16b 16c 16d 16e 16f 16g 16h 16i Density [kg/m3] 33.1 30.8 33.7 31.0 29.9 30.2 40.6 40.6 25.9 Hardness [kPa] 3.6 3.4 3.8 3.4 3.3 3.4 4.5 4.4 3.3 SAG 3.3 3.1 3.6 3.2 3.2 2.9 3.2 3.2 3.0 Airflow [L/sec] 1.1 1.4 1.2 1.3 0.9 1.4 1.0 1.1 1.0 CS dry 50, % 5.1 5.9 7.4 5.9 5.8 5.4 8.2 8.0 8.9 Resilience, % 52.0 50.0 54.0 50.0 48.5 52.0 52.0 50.5 48.5 Cal 117 pass pass pass pass pass pass pass pass pass FMVSS SE DNI DNI DNI SE DNI DNI DNI SE

Examples 17a-17h: Foams Without Melamine Part 2

(112) TABLE-US-00018 TABLE 14 Example No. 17a 17b 17c 17d 17e 17f 17g 17h Ongronat ®1080 [g] 41.31 40.20 40.76 32.23 32.23 32.22 49.27 49.28 FR Polyol Ex. No. 6a [g] 70 — — 70 — — 70 — FR Polyol Ex. No. 6b [g] — 70 — — 70 — — 70 FR Polyol Ex. No. 6c [g] — — 70 — — 70 — — Polyol C [g] 30 30 30 30 30 30 30 30 water add [g] 2.625 2.675 2.65 1.875 1.875 1.875 3.425 3.425 water total [g] 3.1 3.1 3.1 2.3 2.3 2.3 3.9 3.9 DABCO BLV [g] 0.16 0.18 0.18 0.25 0.3 0.2 0.1 0.12 DEOA 90% [g] 1 0.5 0.75 0.5 0.5 0.5 1 1 Ortegol ®204 [g] 1.5 1.5 1.5 1.5 1.5 1.5 1.5 1.5 B 8783 LF2 [g] 0.3 0.3 0.3 0.3 0.3 0.3 0.3 0.3 Kosmos ®29 [g] 0.12 0.12 0.12 0.12 0.1 0.12 0.1 0.1 Rise Time [sec] 143 120 131 150 140 153 112 111

(113) Foam Properties

(114) TABLE-US-00019 TABLE 15 Example No. 17a 17b 17c 17d 17e 17f 17g 17h Density 30.4 31.6 30.8 41.6 42.0 42.6 25.3 25.5 [kg/m3] Hardness [kPa] 2.6 3.0 2.7 3.6 3.3 3.4 2.6 2.6 SAG 3.0 2.9 3.1 3.2 3.3 3.2 2.7 2.7 Airflow [L/sec] 1.9 1.3 1.5 1.5 1.5 1.5 1.4 1.2 CS dry 50, % 6.8 7.9 6.2 6.9 6.3 7.8 9.0 9.5 Resilience, % 54.0 52.0 51.5 53.0 52.5 48.0 51.0 50.0 Cal 117 pass pass pass pass pass pass pass pass FMVSS DNI DNI DNI DNI DNI DNI SE DNI

(115) Examples 18a-18i: Foams Without Melamine Part 3

(116) TABLE-US-00020 TABLE 16 Example No. 18a 18b 18c 18d 18e 18f 18g 18h 18i Ongronat ®1080 [g] 40.92 40.90 40.89 42.00 34.06 34.02 32.92 49.99 49.98 FR Polyol Ex. No. 6a [g] 50 — — 50 50 — — 50 — FR Polyol Ex. No. 6b [g] — 50 — — — 50 — — 50 FR Polyol Ex. No. 6c [g] — — 50 — — — 50 — — Polyol C [g] 50 50 50 50 50 50 50 50 50 water add [g] 2.675 2.675 2.675 2.625 1.825 1.825 1.875 3.425 3.425 water total [g] 3.1 3.1 3.1 3.1 2.3 2.3 2.3 3.9 3.9 DABCO BLV [g] 0.16 0.16 0.14 0.14 0.25 0.2 0.2 0.12 0.12 DEOA 90% [g] 0.5 0.5 0.5 1 1 1 0.5 1 1 Ortegol ®204 [g] 1.5 1.5 1.5 1.5 1.5 1.5 1.5 1.5 1.5 B 8783 LF2 [g] 0.3 0.3 0.3 0.3 0.3 0.3 0.3 0.3 0.3 Kosmos ®29 [g] 0.12 0.12 0.12 0.12 0.16 0.12 0.12 0.12 0.1 Rise Time [sec] 110 113 117 120 120 150 146 100 115

(117) Foam Properties

(118) TABLE-US-00021 TABLE 17 Example No. 18a 18b 18c 18d 18e 18f 18g 18h 18i Density [kg/m3] 34.0 33.9 33.9 33.3 40.7 41.2 41.8 25.0 25.0 Hardness [kPa] 3.7 3.6 3.7 3.4 3.3 3.2 3.6 2.9 2.8 SAG 3.0 3.1 3.1 3.2 3.5 3.0 3.3 2.7 2.8 Airflow [L/sec] 0.2 0.5 0.3 0.6 1.0 1.2 1.3 0.7 0.7 CS dry 50, % 9.2 9.1 8.9 8.4 7.6 7.3 6.5 6.2 6.8 Resilience, % 33.0 45.5 42.5 46.0 52.5 53.0 51.0 48.0 49.5 Cal 117 pass pass pass pass pass pass pass pass pass FMVSS DNI DNI DNI DNI DNI DNI DNI SE SE

Examples 19a-20b: Foams with Melamine

(119) TABLE-US-00022 TABLE 18 Example No. 19a 19b 20a 20b Ongronat ®1080 [g] 31.25 33.31 41.15 32.92 FR Polyol Ex. No. 6b [g] 45 45 45 45 Polyol C [g] — — 55 55 Polyol A [g] 55 — — — Polyol E [g] — 55 — — Melamine [g] 15 15 15 15 water add [g] 1.93 1.93 2.73 1.93 water total [g] 2.3 2.3 3.1 2.3 DABCO BLV [g] 0.18 0.18 0.12 0.18 Ortegol ®204 [g] 1.5 1.5 1.5 1.5 B 8783 LF2 [g] 0.3 0.3 0.3 0.2 Kosmos ®29 [g] 0.15 0.15 0.15 0.12 Rise Time [sec] 125 145 105 128

(120) Foam Properties

(121) TABLE-US-00023 TABLE 19 Example No. 19a 19b 20a 20b Density [kg/m3] 37.8 40.1 31.1 39 Hardness [kPa] 3.4 3.6 4.9 5.1 SAG 2.8 2.9 2.8 3.3 Airflow [L/sec] 0.3 0.36 0.11 0.53 CS dry 50, % 5.3 5 6.5 5.6 Resilience, % 45 47 29 49 Cal 117 Pass Pass Pass Pass FMVSS DNI DNI SE DNI CRIB 5 Pass Pass Pass Pass

Examples 21a-22b: Foams with Melamine

(122) TABLE-US-00024 TABLE 20 Example No. 21a 21b 21c 21d 21e 22a 22b Ongronat ®1080 [g] 45.67 37.68 37.13 37.03 56.68 38.67 57.28 FR Polyol Ex. No. 6a [g] — — 60 — 60 — — FR Polyol Ex. No. 6b [g] 60 60 — — — 70 70 FR Polyol Ex. No. 6c [g] — — — 60 — — — Polyol C [g] 40 40 40 40 40 30 30 Melamine [g] 25 25 25 25 25 25 25 water add [g] 3.03 2.23 2.25 2.26 3.91 2.46 3.83 water total [g] 3.5 2.7 2.7 2.7 4.45 2.9 4.45 DABCO BLV [g] 0.16 0.2 0.2 0.2 0.1 0.2 0.1 DEOA 90% [g] 1 1 0.75 0.7 1.7 0.7 2 Ortegol ®204 [g] 1.5 1.5 1.5 1.5 1.5 1.5 1.7 B 8783 LF2 [g] 0.3 0.3 0.3 0.3 0.3 0.3 0.3 Kosmos ®29 [g] 0.15 0.14 0.14 0.16 0.13 0.16 0.13 Rise Time [sec] 120 140 140 150 120 123 122

(123) Foam Properties

(124) TABLE-US-00025 TABLE 21 Example No. 21a 21b 21c 21d 21e 22a 22b Density [kg/m3] 34.5 46.1 46.2 47.1 27.5 39.7 28.1 Hardness [kPa] 5.68 6.8 7.07 6.74 4.45 4.84 3.87 SAG 3.19 3.82 3.63 3.48 2.76 3.43 2.98 Airflow [L/sec] 0.56 0.53 0.65 0.94 0.42 1.2 0.55 CS dry 50, % 28.7 24.7 28.4 30.4 19 12.3 30.1 Resilience, % 44 51 49 51 45 51 48 Cal 117 Pass Pass Pass Pass Pass Pass Pass FMVSS DNI DNI DNI DNI DNI DNI SE CRIB 5 Pass Pass Pass Pass Pass Pass Pass

Examples 23a-23e: Moulded Foams

(125) TABLE-US-00026 TABLE 22 Example No. 23a 23b 23c 23e Ongronat ®1080 [g] 39.73 39.74 31.77 32.88 FR Polyol Ex. No. 7b [g] 100 — 100 — FR Polyol Ex. No. 13 [g] — 100 — 100 Melamine [g] 15 15 15 15 water add [g] 2.675 2.675 1.875 1.825 water total [g] 3.1 3.1 2.3 2.3 DABCO BLV [g] 0.15 0.15 0.18 0.18 DEOA 90% [g] 0.5 0.5 0.5 1 Ortegol ®204 [g] 1.5 1.5 1.5 1.5 B 8783 LF2 [g] 0.3 0.3 0.3 0.3 Kosmos ®29 [g] 0.13 0.15 0.18 0.18 Rise Time [sec] 100 100 109 106

(126) Foam Properties

(127) TABLE-US-00027 TABLE 23 Example No. 23a 23b 23c 23e Density [kg/m3] 30.4 30.4 40.9 39.7 Hardness [kPa] 2.4 2.6 2.8 2.5 SAG 3.1 3.1 3.4 3.5 Airflow [L/sec] 0.68 0.46 0.56 0.65 CS dry 50, % 9.1 7.5 6.6 7.5 Resilience, % 51 51 55 55 Cal 117 Pass Pass Pass Pass FMVSS DNI SE DNI DIN CRIB 5 Pass Pass Pass Pass