NO161668B - PROCEDURE AND PLANT FOR SEPARATION AND STORAGE OF OIL AND GAS IN EXPLOSED MOUNTAIN ROOMS UNDER THE GROUND WATER LEVEL. - Google Patents

Description

Process for precipitation of finely divided, infusible and insoluble melamine-formaldehyde condensation products.

The invention relates to another method

precipitation of finely divided, infusible and insoluble

melamine-formaldehyde condensation products

with an average particle size below 1 micron from an aqueous solution of a precondensation product of 1 mole of melamine and 1.5 to 6 moles

formaldehyde, preferably from an aqueous solution containing 5-25% by weight of resin-forming components, and the method is

characterized by the precipitation occurring in the presence

of a protective colloid in the pH range 6.0 to 8.0,

preferably 6.0 to 7.0, and preferably at the boiling temperature of the reaction medium.

Usually the precipitate formed is known

manner separated, dried and deagglomerated. However, for certain applications in aqueous systems, e.g. as textile matting agents, too

be advantageous to apply the precipitate in it

form as it directly appears.

By the method according to the invention,

one powdery, solid substances with average particle sizes that are usually well below 1 micron. They are well suited as reinforcing fillers for natural and synthetic rubber and for thermoplastic plastics, such as e.g. polyethylene, as fillers for hardenable plastics and as a matting agent for textiles as well as a thickening and thixotroping agent. The finely divided resin powders produced according to the invention are white, light-resistant, have a low volume weight and, compared to inorganic solids such as e.g. silica gel, titanium dioxide, calcium carbonate, also a low specific gravity (d2o = 1.46). They are highly resistant to heat, water, alkalis, acids and solvents and are not physiologically dangerous.

Instead of formaldehyde, its polymers such as para-formaldehyde or other formaldehyde-releasing substances can of course be used in a known manner.

The properties of the finely divided resin powders can, if desired to adapt the properties for specific applications, be modified by co-condensation with other substances participating in the resin formation. In particular, there is a partial replacement of the melamine with other amino plastic formers, and also a partial replacement of formaldehyde with other aldehydes.

As aminoplast formers, which can partially replace the melamine, the following come into consideration: urea, thiourea, guanidine, dicyandiamide and dicyandiamidine, further alkyl and cyclic alkyleneureas, further from melamine various aminotriazines, such as melam, melem, ammelide and ammelin, substituted melamines , such as butyl or phenylmelamine as well as guanamines, such as acetoguanamine, ibenzoguanamine, tetrahydrobenzoguanamine and stearoguanamine.

As aldehydes, which can replace formaldehyde or its polymeric part, it can e.g. are used: acetaldehyde, (iso)-butyraldehyde, acrolein, crotonaldehyde, furfurol and glyoxal.

For special application purposes such as e.g. for rubber reinforcement, however, the melamine-formaldehyde condensation products can also be modified with the following other co-condensable substances: lower aliphatic alcohols such as methanol, ethanol, butanol, phenols and alkylphenols, such as phenol, resorcinol, bisphenol A, cresols, xylenols , amides of saturated and unsaturated aliphatic carboxylic acids, CH-acSde compounds such as e.g. acet-acetic ester and many sulfur compounds such as ammonium rhodanide, ammonium sulphide, thioformaldehyde.

According to the invention, the presence of a protective colloid during precipitation of melamine-formaldehyde condensation products is necessary. A protective colloid is understood to mean a macromolecular, water-soluble, organic substance which can also have a polyelectrolyte character. Examples of such protective colloids are natural substances such as starch, gelatin, glue, tragacanth and agar-agar, modified natural substances, such as the alkali salts of carboxymethylcelluloses or alginic acid, further synthetic high polymers such as polyvinyl alcohol, polyvinylpyrrolidine, the alkali salts of polyacrylic acid, of polymethacrylic acid and the copolymers of acrylic acid and methacrylic acid, salts of copolymers of maleic acid, polyhydrochlorides of homo- or copolymers of vinylpyridine. The protective colloid concentration necessary to obtain a finely divided precipitate depends on the type of the protective colloid, its molecular weight and on the concentration of the resin former. It can vary within wide limits, for example between 0.01% and 10% calculated on the total amount of the mixture. High-molecular protective colloids, which strongly manage to increase the viscosity of aqueous solutions, already work in smaller concentrations. A higher concentration of the resin former also necessitates a higher concentration of the protective colloid.

For carrying out the method according to the invention, melamine and formaldehyde are reacted, in a molar ratio of between 1.5 and 6, in aqueous solution. The aqueous solvent medium preferably consists of water alone, however, solvent mixtures can also be used which, in addition to water, contain other water-compatible, inert solvents, e.g. lower alcohols such as methanol. The protective colloid can be added from the beginning, and the resin former can be reacted directly to form a precipitate (one-step method). However, one can also, as is often common in aminoplastic chemistry, first form a precondensate of melamine and formaldehyde or other modifying substances, and possibly after dilution let it further react at a constant pH value to form a precipitate, as the protective colloid can only be added after the formation of the pre-condensate (2-stage procedure).

It has surprisingly been found that the finely divided precipitation is obtained at pH values between 6 and 8, especially between 6 and 7. Above pH

= 8, the tendency for resin formation is very small (see e.g. A. Gams, G. Widmer, W. Fisch, Heiv.

Chem. Acta 24, 302 E-319 E (1941). Below pH = 6, precipitates of inhomogeneous particle size distribution with coarse parts above 1 micron are usually obtained. Due to the strong pH dependence of the average particle size, it is therefore appropriate to have a suitable pH stabilization device (consisting of a glass electrode, pH measuring device and automatic burette). Such a technique is preferable for the use of buffer substances, as the latter would first have to be washed out after completion of precipitation.

The precipitation can be carried out in dilute to slightly concentrated solutions. Above 25%, the reaction mixture is very thick and difficult to stir and homogenize. Concentrations of resin formers between 5 and 25 percent by weight are therefore preferred.

The boiling temperature of the reaction medium has proven to be the best precipitation temperature. Precipitation below boiling temperature is also possible, however longer reaction times must be taken into account when good yields are to be achieved. Unprecipitation above 100° C under pressure necessitates special equipment precautions.

The precipitate is best separated by filtration or centrifugation. A small addition of salts of polyvalent metals such as aluminum sulphate often facilitates this operation. The precipitates are dewatered by drying in a stream of air or also azeotropically using benzene, toluene etc., and then dried. The deagglomeration can be effected in a known manner by ball, impact or air jet mills.

The resin powders produced by the method according to the invention have approximately spherical single particles, their average diameter a

can be calculated according to the powder's specific surface according to

It usually agrees well with the electron-optical particle size determination.

In the following examples, the pH values are corrected to 20°C.

Example 1:

a) Preparation of a pre-condensate:

A mixture of 480 g of a 30% by weight aqueous formaldehyde solution and 4.8 g of a 50% by weight aqueous solution of monoethanolamine phosphate with 2n-NaOH is adjusted to pH = 6. Then 151 g of melamine is added, heated under stirring at 60° C and condenses within 30 minutes at this temperature. After the melamine has dissolved, the pH value is 6.9.

b) Precipitation:

The reaction vessel is equipped with a stirrer,

a reflux cooler, a thermometer, a dropping funnel and a glass/calomel electrode pair, which is connected to a pH measuring device and a solenoid valve which, when a predetermined pH value is exceeded, releases the supply of 10% sulfuric acid.

One fills in: 4,900 ml of H20 and 6 g of a sodium salt of a carboxymethylcellulose. which in a 1% by weight aqueous solution has a viscosity of at least 1300 cP.

Heat to a gentle boil, as the protective colloid dissolves. The automatic pH regulation is switched on to pH = 6.0. The precondensate produced according to point a) is allowed to flow from the drop funnel so that the temperature does not fall below 90° C and the pH value does not fall below 5.9. Towards the end of the addition of the pre-condensate, a turbidity forms which immediately condenses into a precipitate. It is left to react for 16 hours at 90° C and pH = 6.0, cooled to room temperature, suctioned off, washed with water, dried at 80° C to constant weight and ground for 90 minutes in a ball mill.

You get 201 g of a white powder with a volume weight of 74 g/l and a specific surface area of 83.2 m2. g—<1> and an average particle size of 49 millimicrons.

Example 2 — 4:

The effect of the pH value on precipitation: You proceed exactly as indicated in example 1, but carry out the precipitation and the post-reaction at other pH values.

In example 4, the same amount of tragacanth was used instead of Na-carboxymethyl cellulose.

Example 5 — 9:

Effect of different protective colloids: Proceed exactly as indicated in example 1, however, instead of sodium carboxymethyl cellulose, the protective colloids indicated in the following table II are used. The precipitations and the post-reaction are carried out at pH = 6.5.

Example 10 — 14: Influence of the molar ratio formaldehyde: melamine.

For example 10 with a molar ratio of formaldehyde : melamine = 2, the following mixtures and process conditions were used: a) Precondensate 240 g of a 30% by weight aqueous solution of CH20 2.4 g 50% by weight aqueous solution of a basic monoethaneblamin phosphate in 151 g melamine 30 minutes 60° C and pH = I 6.9. b) Precipitation at pH = 6.5 and 90° C in: 5140 g H20 25 g gelatin. j Otherwise, you proceed in the same way as ;

indicated in example 1..

In the following examples 11-14, the amount of formaldehyde corresponding to the higher molar ratio was increased, the amount of water was decreased by the same amount to keep the concentration constant.;

Mixture and test results appear in table i

III. IN

IN

Example 15: Entry procedure in concentrated solution: 3640 g of H20 and 16 g of a copolymer of maleic anhydride and styrene, the preparation of which is described below, are introduced and heated to boiling. 6.5 ml of 24% by weight aqueous ammonia is adjusted to pH = 7.3 and 378 g of melamine is added. The pH stabilization device is set to pH = 6.5 and 1500 g of aqueous 40% by weight formaldehyde solution is dripped in at 90° C. During this phase, 2n-NaOH must be delivered from the automatic burette. 55 g of 2n-NaOH are consumed. As soon as all the formaldehyde has been added, a clear solution is obtained. After approx. After 16 minutes at 90-95° C, a cloud appears which thickens to precipitate. The lye burette is replaced with an acid burette (10% H2S04). The reaction mixture now assumes the consistency of a thixotropic gel. The acid supply is interrupted during this phase. The gel is stirred at a higher speed into a porridge and left to react for 16 hours at 90-95° C and pH = 6.5 to 6.6.

It is cooled to 25° C, centrifuged, dried at 80° C in a stream of air, ground within 90 minutes in a ball mill and sieved.

The protective colloid used in this example is prepared as follows: 98 g of maleic anhydride is heated,

4.04 g of dibenzoyl peroxide and 1325 ml of toluene to boil, add 104 g of styrene drop by drop and continue to boil for 3 hours. The polymer is then filtered off and dried at 80° C to a constant weight. Exchange: 199.5 g.

Claims (3)

i 1. Process for the precipitation of finely divided, I insoluble and insoluble melamine-formaldehyde j condensation products with an average particle size below 1 micron from an aqueous j solution of a precondensation product of 1 mol of melamine and 1.5 to 6 mol of formaldehyde, step by step from an aqueous solution containing 5-25% by weight of resin-forming components, characterized in that the precipitation takes place in the presence of a protective colloid in the pH range 6.0 to 8.0, preferably 6.0 to 7.0 , and preferably at the boiling temperature of the reaction medium. 2. Method according to claim 1, characterized in that gelatin or a high molecular weight polycarboxylic acid or its alkali salt is used as a protective colloid, preferably carboxymethyl cellulose or a saponified j copolymer of maleic anhydride and styrene > in the form of the free acids or their alkali salts. j 3. Method according to claims 1-2, characterized in that the protective colloid is used in amounts from 0.01 to 10 percent by weight, calculated on the total amount of aqueous reaction! tion mixture.