Patent Grant
7087670
The invention relates to mixtures containing
The term flame-retardant intumescent mixtures refers to foaming flame-retardant mixtures, in other words mixtures which foam to a certain extent upon exposure to fire and have flame-retardant properties.
Mixtures of this type may be used, for example, in joints in buildings and ruptures in cables, cavities, holes, transitions and connections in walls of buildings or fire safety components such as claddings to prevent the spread of the fire, conflagration gases and smoke in the event of fire. Components made of these mixtures are therefore used for preventive fire safety.
The expanding behaviour of these compounds in the event of fire can also make a particular contribution to the preservation of shape or function of, for example, ceiling and wall claddings, because the components are compressed by expanding profiles and sealing members.
These mixtures have to have further properties, for example water resistance. Therefore, conventional flame retardants such as water-soluble polyphosphates are usually undesirable. The extent of foaming also has to remain unchanged over very long storage times.
It is known from JP-B-95068362 to use expanded graphite as flame-retardant component in mixtures of vulcanised acrylate rubber. JP-B2-95103948 describes vulcanised acrylate rubber materials with expanded graphite for producing flame-retardant hoses.
Expanded graphite rubber mixtures based on polychloroprene with 30 phr (per hundred rubber) maximum expanded graphite and therefore excessively small proportions of this filler are described in JP-A-10036572. Furthermore, the use of halogen-containing components is undesirable nowadays.
JP-A-09176579 describes mixtures with EVA (10 to 50% VA) or m-PE with phosphorus and expanded graphite and mineral filler for adhesive tapes round pipes through wall apertures. Red phosphorus is invariably used. However, red phosphorus is difficult to process. In addition, red phosphorus may continue to react after processing.
The object of this invention was to find a phosphorus-free, in particular red phosphorus-free mixture which withstands the necessary fire safety tests, has adequate expanding behaviour, is waterproof and allows simple shaping, for example by extrusion, calendering, compression moulding, etc.
Furthermore, the shaped articles to be produced should have adequate dimensional stability but still be deformable to a certain extent, to still allow adaptation to the protective substrates or insertion into the joints in the component or building during construction and assembly.
A further object was to avoid the need for further vulcanisation or maturing periods to enable the article to be used immediately after shaping. A further object was accordingly to provide unvulcanised mixtures having adequate stability of shape while being deformable to a certain extent by the user.
In addition, it was desired to use substantially halogen-free feedstock for producing these mixtures.
The objects set are achieved according to the invention by providing mixtures containing,
It is preferable to use ethylene vinyl acetate copolymers as polymer a).
The polymer a) can be produced by conventional methods, for example by radical copolymerisation in solution, emulsion or mass.
The content of vinyl acetate incorporated by polymerisation should advantageously lie in the range from 50 to 85 wt. %, and mixtures of these polymers with a different vinyl acetate content may also be used.
Ethylene methyl acrylate polymers optionally also containing further comonomers may also be used instead of or in addition to ethylene vinyl acetate polymers optionally containing further comonomers.
To achieve high fire retardance, it is advantageous to use an ethylene vinyl acetate copolymer or an ethylene methyl acrylate copolymer.
Maximum fire retardance is achieved with particularly high contents of polar comonomer.
Further comonomers which are optionally present include, in particular, vinyl esters of higher carboxylic acids and also longer chain (meth)acrylates, the content of these monomers in the polymer generally being higher, the greater the non-polar organic group content in the polymer, to ensure the desired flame retardance. Furthermore, CO is also mentioned as monomer component.
However, the glass transition temperature of the terpolymers obtainable in this way should be taken into consideration when selecting the additional monomers. If it is at ambient temperature or above ambient temperature, mixtures produced from it are generally brittle and therefore difficult to use at typical service temperatures. It is also possible to use so-called acrylate rubbers as polymer a).
A useful upper limit for the glass transition temperature of 15° C. is generally achieved for the ethylene vinyl acetate copolymers containing 85 wt. % of vinyl acetate.
The flexibility of shaped articles made of the mixtures according to the invention can obviously also be influenced by addition of further plasticising additives which are mentioned hereafter.
Expanded graphites produced by sulphatising or nitration of graphite can advantageously be used as so-called expandable graphite b). These expanded graphites are known to a person skilled in the art and can be used for achieving fire retardance in scaling compounds, coatings and in general in thermoplastic materials. They are typically used, for example, in polyurethanes (see the brochure entitled Kurzliefer-programm Flammschutzmittel, Brandschutzartikel, produced by Nordmann and Rassmann in January 2000).
Expanded graphites are layered graphites which can be reacted with sulphuric acid or nitric acid or generally strong acids under oxidising conditions. Water-soluble salts are produced in the layer lattice of the graphite. The reaction with sulphuric acid and H2O2 is typical. These reaction products are then usually washed free of acid using water, wherein the amount of remaining acid below 1 mg/g is to be measured as KOH. Neutral expanded graphites are obtained by additional neutralisation (for example with sodium hydroxide solution or ammonia), this material also being washed again to remove adhering neutralising agent. Neutral types have a pH of at least 6.
The advantageous use of expanded graphite for fire safety is based on
The mineral fillers can basically be selected freely, energy-consuming fillers such as aluminium hydroxides, magnesium hydroxides or calcium carbonate providing additional contributions to fire retardance. However, talcum, silicas, silicates, carbonates and sulphates can also be used. Mixtures of the aforementioned fillers may obviously be used.
Typical additives include processing aids such as stearic acid, waxes, lubricating waxes, oils and release agents or also flame-retardant additives such as phosphoric acid ester, ammonium polyphosphates, antimony bromide, etc., halogen-containing fire retardants being less preferred. Water-soluble additives are less preferred owing to the waterproofing.
The use of unneutralised expanded graphites together with ethylene vinyl acetate copolymers can lead to partial hydrolysis with formation of acetic acid. Basic oxides and carbonates or other acid receptors may be added to prevent the liberation of acetic acid.
Non-polar, substantially saturated elastomers such as EPM, EPDM, butyl rubber, hydrated or partially hydrated SBR rubbers can also be used as additives, but advantageously in at most half the amount of a). An advantage of the mixtures is that they allow a relatively wide variation in the amounts of expanded graphite and, in particular, of other mineral fillers which have an energy consuming effect on exposure to fire. Particularly large amounts of components b) and c) can also be achieved in this way. In contrast to the state of the art, surprisingly, component b) can be used in an amount in the range of 50 to 200 parts by weight and component c) in an amount in the range from 50 to 500 parts by weight, based on 100 parts by weight of a) in each case, without sacrificing the good properties, in particular mechanical and processing properties. High demands with regard to fire performance can therefore be achieved. In addition, the raw material costs of such a mixture can be favourably influenced as mineral fillers are usually relatively inexpensive.
The polymers a) used additionally probably have the function of an effective binder which allows large amounts of filler including expanded graphite to be compounded to a processible mixture.
The invention also relates to a process for producing the mixtures according to the invention by mixing the individual components in any sequence in a conventional mixing unit such as an internal mixer, a roller, a screw or a kneader. It may be advantageous to provide cooling during the mixing process to prevent the mixture from becoming too hot. The polymers a) according to the invention allow the production of mixtures without using excessively high shearing forces which could adversely affect the structure of the expanded graphite.
The invention also relates to the use of the mixture for producing shaped articles of any type such as films or sheets of various thickness or profiles of differing geometry, and as a material for cementing joints in buildings and ruptures in cables, cavities, holes, transitions and connections in walls of buildings or for producing fire safety components such as claddings.
An advantage of the mixture according to the invention is that the shaped articles can be produced by continuous processes as the mixtures have a sufficiently wide processing window during processing. This means that, in particular, premature foaming can be avoided during shaping. Extrusion, optionally multi-layer extrusion, and calendering are preferred processing methods. The invention also relates to the aforementioned shaped articles. It may be necessary to vulcanise the mixtures according to the invention in order to produce the shaped articles. This is carried out in a manner known to the person skilled in the art and is described, for example, in “Vulkanisation & Vulkanisationshilfsmittel (W. Hofmann, Leverkusen 1965, p. 85 ff, 225 ff). The vulcanisation system must be selected according to the type of polymer a). Peroxide vulcanisation or, in general, vulcanisation using radical forming agents should be selected in the case of ethylene vinyl acetate copolymers. This includes vulcanisation by high-energy radiation. The normal recommendations can be followed when carrying out vulcanisation in the case of ethylene methyl acrylate copolymers. Sulphur vulcanisation can also be employed if a) contains double bond-containing polymers.
The invention also relates to flame-retardant incumescent mixtures containing a mixture according to the invention.
The following examples serve to illustrate the invention.
Feedstock Used:
The mixtures were produced as follows:
The quantities of components of the mixture were calculated for a total quantity of 200 to 300 g.
The mixture was mixed at about 20° C. on a laboratory roller in that the polymer was presented and initially subjected to a few passes through the roller, the stearic acid, expanded graphite and Apyral were then added in succession and the mixture removed from the roller after a total mixing period of 15 min.
Test pieces were pressed from the mixtures, as specified, two different press conditions being selected.
A pronounced odour of acetic acid was perceived during production of the mixtures. The test pieces were flexible and could be bent without breaking.
Evaluation of Results:
Intumescence which is as uniform as possible and minimal destruction of the samples is desired. Mixtures 1a to 1b show that mixtures of Levapren and expanded graphite can additionally be highly filled with a flame-retardant filler such as Apyral. The mixtures obtained are readily processible and exhibit uniform intumescence in the flame test. Mixtures 1c and 1d are particularly good here. The formation of blisters or buckling during the flame test depends on the pressing conditions. In mixture 1d, with 400 phr, the optimum quantity of Apyral is obviously exceeded. To avoid heat transfer, it is obviously advantageous to use Apyral, the quantity preferably being 50 phr or higher.
The mixtures were produced as in Example 1 but the temperature set at 50° C. during production of the mixture.
It was found that only mixtures with up to 70 phr expanded graphite could be produced. The test pieces obtained had a very irregular surface. This could sometimes be improved if pressing was carried out at elevated temperature (100° C.) and for a prolonged period (30 min).
It was only possible to produce mixtures with up to 70 phr of expanded graphite. As shown in the table, Enerthene 1849-1, a mineral oil, had to be added.
An attempt was also made to use a flame-retardant processing aid with Disflamol DPK (diphenyl cresyl phosphate). It is found that this aid was not compatible with the compound and even complicated incorporation of the expanded graphite. The highly filled EPDM compounds continued to smoke and this was a disadvantage for the application according to the invention.
Evaluation of Results:
Processible mixtures may be obtained with EPDM only with expanded graphite quantities below 70 phr. Acceptable shaped articles could be obtained only after prolonged pressing, but blistering was then observed in the flame test. The mixture was extremely difficult to produce owing to poor filler/expanded graphite uptake. In contrast to mixing batch 1, it will probably be difficult to bring mixtures from batch 2 into the manifold forms desired by the user.
The additions of Apyral surprisingly impaired the fire performance because after-glowing was observed.
The mixtures were produced as in Example 1. The feedstock was mixed in on the roller in the sequence as in the table.
The odour of acetic acid was not perceived during production of the mixtures. The samples from Examples 3a to 3m were tested in accordance with UL 94V-0 (Underwriter Laboratories, see
The results of this test show that excellent flame retardance can be achieved. Adequate intumescence is also found, in order to create the necessary seal in the event of fire. Additional finish involving flame-retardant components such as phosphate esters or antimony compounds etc. is not necessary. The mixtures are halogen free.
It was also found in Example 3l and 3m that an exceptionally high degree of filling is possible with Apyral as a typical representative of a mineral filler. This further increases flame retardance, as demonstrated by extremely low destruction of material.
An odour of acetic acid as in Example 1, which can be explained by partial hydrolysis of the Levapren, can be avoided by addition of a mineral basic acid receptor or by the use of neutral expanded graphite.
The roller temperature was 20° C. and the press temperatures 70, 75, 80, 100 and 150° C. The processibility of the compounds was good.
Levapren 800 HV can be used for intumescent mixtures, similarly to Levapren 700 HV. However, the constitution of the sheets/test pieces was more homogeneous with Levapren 700 HV.
It has generally been found that all EVA compounds could be processed more readily than the corresponding EPDM compounds.
| Number | Date | Country | Kind |
|---|---|---|---|
| 100 24 421 | May 2000 | DE | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP01/05144 | 5/7/2001 | WO | 00 | 11/15/2002 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO01/88029 | 11/22/2001 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 3574644 | Olstowski et al. | Apr 1971 | A |
| 5719199 | Wallace et al. | Feb 1998 | A |
| 6410122 | Tono et al. | Jun 2002 | B1 |
| Number | Date | Country |
|---|---|---|
| 41 35 678 | May 1993 | DE |
| 03041163 | Feb 1991 | JP |
| 03041164 | Feb 1991 | JP |
| 07068362 | Jul 1995 | JP |
| 95103948 | Nov 1995 | JP |
| 9-176579 | Jul 1997 | JP |
| 10-36572 | Feb 1998 | JP |
| Number | Date | Country | |
|---|---|---|---|
| 20030125447 A1 | Jul 2003 | US |
