Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Processes of preparing a desired or intentional composition...
Reexamination Certificate
1999-09-07
2001-08-14
Nutter, Nathan M. (Department: 1711)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
Processes of preparing a desired or intentional composition...
C524S037000
Reexamination Certificate
active
06274653
ABSTRACT:
FIELD OF THE INVENTION
The present invention relates to new cellulose nitrate/plasticizer combinations comprising 82-40 wt. % cellulose nitrate with a nitrogen content of less than 12.6 wt. % and 18-60 wt. % formylated polyurethanes as plasticizers.
BACKGROUND OF THE INVENTION
Cellulose nitrate is known as an essential constituent of many paint systems (cf. e.g. U. Biethan, Lacke und Lösemittel [Paints and Solvents], Verlag Chemie GmbH, Weinheim, 1st edition, 1979, p. 8).
Since cellulose nitrate in the dry form can be made to ignite very easily by impact or friction, commercially available paint cellulose nitrates must be treated either with a stabilizing agent (e.g. humidifying agent) in an amount of at least 25 wt. % or a gelatinizing plasticizer in a concentration of at least 18 wt. % in order to reduce risks during storage, handling and transportation.
In addition to water, in general alcohols, such as ethanol, isopropanol and butanol, are used as humidifying agents. However, in the processing of paints containing cellulose nitrate, alcohols cause trouble in the conventional adsorption units installed downstream of painting units to reduce emissions. Alcohols also cause trouble when used in PU paints. They react with isocyanates to give low molecular weight compounds, as a result of which the quality of the paint film is reduced significantly.
DE-A 30 41 085 and U.S. Pat. No. 3,284,253 describe cellulose nitrates which contain inert solvents (e.g. toluene) as a humidifying agent. They are prepared by means of a distillative working step, which is exceptionally expensive and presents safety problems.
All cellulose nitrates provided with humidifying agents continue to have the problem of evaporation of the humidifying agent or inhomogeneous distribution as a result of sagging during storage in a drum.
So that the user has a free choice of solvent which can be employed, cellulose nitrate is also available in plasticized form (so-called NC chips). These NC chips are generally prepared by incorporating plasticizers into water-moist cellulose nitrates. The preparation is described e.g. in DE 1 203 652, DE 1 570 121, DE 1 470 860 and DE 2 338 852.
Prerequisites for the preparation of NC chips are gelatinizing plasticizers in a pure form or those plasticizers which acquire gelatinizing properties by an addition of organic solvents which dissolve cellulose nitrate. These organic solvents are removed again during drying. Environmental technology measures are therefore necessary in such a preparation process, in order to ensure the legally required emission values and explosion limits are adhered to.
In addition to the gelatinizing power of the plasticizers with respect to the cellulose nitrate, additional plasticizer properties such as acceptability in terms of foodstuffs legislation, resistance to migration and good general mechanical and chemical properties are required by the market as a basic prerequisite for the preparation of NC chips.
It is known that polyurethanes meet a large number of the properties required. They are distinguished e.g. by good resistance to chemicals, resistance to heat, fastness to light (in the case of polyurethanes based on aliphatic isocyanates) and very good mechanical properties.
The preparation of cellulose nitrates plasticized with polyurethane oils is described in DOS 2 215 624. According to the invention, an aqueous suspension of the plasticizing agent is brought together with an aqueous suspension of cellulose nitrate fibres with vigorous stirring. The resulting product is filtered off, squeezed off, shaped by calendering, dried and cut to chips. Anionic and/or nonionic emulsifiers are employed for the preparation of the suspension of the plasticizing agent, and these remain in the NC chips after the preparation process and impair in an undesirable manner the resistance to chemicals and in particular the resistance to water of coatings produced therefrom.
To avoid the disadvantages described, it would be desirable to be able to prepare such NC chips by direct application of polyurethane plasticizers on to the NC fibres. However, this has hitherto not been possible because of the lack of gelatinizing power of polyurethane plasticizers or polyurethane oils known to date.
SUMMARY OF THE INVENTION
The aim of the present invention was to allow a direct and therefore economical application to the NC fibres by using specially modified polyurethane plasticizers, and to arrive at a homogeneous and uniformly gelatinized product without having to resort to additional aids such as organic solvents or emulsifiers.
Surprisingly, it has been found that by using formylated polyurethanes, the gelatinizing power of these polymeric plasticizers with respect to nitrocellulose can be increased, so that the abovementioned object is achieved.
DETAILED DESCRIPTION OF THE INVENTION
Formylated polyurethanes are obtainable, e.g., under the commercial name CENTROPLAST® formylated polyurethane, and are distinguished by fastness to light, resistance to heat and non-hydrolysability. They furthermore have FDA and BGA [German Board of Health] approval. The molecular weights of these plasticizers are between 900 and 2,000 g/mol.
Cellulose nitrates with a nitrogen content of less than 12.6 wt. % are employed for the preparation of the cellulose nitrate/plasticizer mixtures according to the invention. Commercially available cellulose nitrates of various viscosity levels with a nitrogen content of 10.0-12.6 wt. % are particularly preferred.
Preferred cellulose nitrate/plasticizer formulations of the type according to the invention are those which comprise 82-40 wt. % cellulose nitrate and 18-60 wt. % pasticizer based on formylated polyurethanes.
In the cellulose nitrate/plasticizer combinations according to the invention there is the possibility of replacing some of the formylated polyurethane by other plasticizers known for cellulose nitrate (cf e.g. A. Kraus, Handbuch der Nitrocelluloselacke [Handbook of Nitrocellulose Paints], Part 3: Weichmachungsmittel [Plasticizers], Wilhelm Pansegrau Verlag, Berlin-Wilmersdorf, 1961). Suitable other plasticizers are, inter alia, phthalates, such as e.g. dibutyl phthalate or dioctyl phthalate, citric acid esters, such as e.g. acetyl tributyl citrate, phosphoric acid esters, such as e.g. 2-ethylhexyl diphenyl phosphate, adipates, such as e.g. diisobutyl adipate, sebacates, such as e.g. dibutyl sebacate, epoxidized or ethoxylated esters of naturally occurring fatty acids or triglycerides, such as e.g. epoxidized soya bean oil (ESO) or ethoxylated castor oil, sugar derivatives, such as e.g. sucrose acetate isobutyrate (SAIB), and glycerol derivatives, such as e.g. glycerol di- or triacetate.
The cellulose nitrate/plasticizer combinations according to the invention are prepared by direct application of the plasticizer on to the water-moist cellulose nitrate in a mixer which does not have a compacting effect, such as is described in DE 1 203 652 and the following examples.
The invention also provides the use of the new NC chips as a paint raw material for coating any desired substrates. For adaptation to particular profiles of requirements the NC chips according to the invention can be combined here with further paint raw materials. Examples which may be mentioned are the use of the paint binder formulations according to the invention in paints for wood, paper, leather, textiles and films and in printing inks.
The paints are applied by the conventional methods of paint technology, such as e.g. spraying, pouring, dipping or rolling.
The following examples are intended to illustrate the invention without limiting it.
REFERENCES:
patent: 3284253 (1966-11-01), Ender et al.
patent: 3948675 (1976-04-01), Rat et al.
patent: 4483714 (1984-11-01), Yamaue et al.
patent: 5362313 (1994-11-01), Hoppe et al.
patent: 5484826 (1996-01-01), Kressdorf et al.
patent: 1203652 (1965-10-01), None
patent: 1470860 (1969-02-01), None
patent: 1051561 (1966-12-01), None
Hecht Reinhold
Hoppe Lutz
Luhmann Erhard
Franks James R.
Gil Joseph C.
Nutter Nathan M.
Preis Aron
Wolff Walsrode AG
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