WO2007089170A1

WO2007089170A1 - Method for producing long-life waterproof foam glass and expanded plastics

Info

Publication number: WO2007089170A1
Application number: PCT/RU2007/000014
Authority: WO
Inventors: Andrey Alexeevich Klimov; Dmitry Andreevich Klimov; Evgeniy Andreevich Klimov; Tatiana Vitalyevna Klimova
Original assignee: Andrey Alexeevich Klimov; Dmitry Andreevich Klimov; Evgeniy Andreevich Klimov; Tatiana Vitalyevna Klimova
Priority date: 2006-01-17
Filing date: 2007-01-15
Publication date: 2007-08-09
Also published as: RU2006101087A; RU2332364C2

Abstract

The invention relates to a method for producing foam glass and expanded plastics exhibiting for many years a low heat conductivity and acoustic permeability and good light transmission values. The inventive method consists in melting a glass or plastic material adding high-hygroscopic agents such as anhydrous CaO, BaO and Al2O3, in cooling the melt to a temperature of 950-1200°C, in expanding the melt in a vessel by passing a superheated multijet stream of vapour of the same temperature therethrough, in mixing the plastic melt with additives of anhydrous CaO, BaO and Al2O3 , in expanding it by means of a water steam at a temperature of the plastic material melting point, in mechanically breaking bubbles in the melting such a way that the diameter thereof is equal to 1-5 mm and the wall thickness ranges from 0.05 to 1 mm and in pressing a foam material into moulds whose internal walls are coated with agents preventing the adhesion of the foam material thereto.

Description

METHOD FOR PRODUCING LONG-LASTING WATERPROOF FOAM GLASS AND FOAM PLASTICS

The invention relates to a method for manufacturing effective, heat-insulating, durable, lightweight foam materials, namely, foam glass and polystyrene and various compositions thereof, and for the disposal of glass and plastic waste resulting from human and household activities.

The foam materials we offer are applicable for thermal insulation both from heat and cold, for fire and chemical protection, and at the same time can be used as sound-absorbing, architectural and structural building material. In many cases, foamy materials are required to be light-transmitting, moisture-proof, heat-resistant, and durable. Foam glass, unlike materials based on wood and plastic, is not subject to decay and chemical decay, resistant to various insects, rodents, does not emit hazardous products in case of fire and aging. The foam materials offered by us can be made with good soundproofness and thermal insulation, capable of transmitting light and suitable for the manufacture of greenhouses and windows, unlike those made using existing technologies.

The quality of foam glass depends on its density, size and distribution of bubbles, their wall thickness, degree of water resistance, light transmission and

DP-

The disadvantages of foam glass produced by existing technologies include: inability to transmit light; the relative high cost of products from it due to the high cost of grinding to particles with a diameter of less than 20 microns and glass making with various additives; long thermal processing of ingredients into block foam glass; large waste when cutting blocks into products of the required styles and sizes; a high proportion of permeable walls of the bubbles, which results in the inability of the foam glass to withstand more than several tens of freeze-thaw cycles.

The most common is the production of block foam glass from specially welded and granular glass, which use scarce and expensive ingredients to improve its properties. It is considered acceptable to involve no more than 20% of certain types of glass waste in the charge. It is argued that obtaining high-quality block foam glass from recyclable container glass waste is a big problem (B. K. Demidovich. Foam glass. - Minsk: Science and Technology, 1975).

In some cases, foam glass is obtained by mixing finely ground glass with a foaming agent, which may contain a reducing agent in the form of a carbon ingredient and an oxidizing agent from sulfates, oxides, etc. The mixture is heated to its melting point. During the heat treatment, a redox reaction occurs between carbon and sulfates (oxidizing agents) and / or glass oxides. As a result, gases SO ₂ , CO ₂ , N ₂ , H ₂ S, etc. are formed in the glass melt, which form bubbles and impart a porous structure to the mass, which leads to the formation of materials with low density and thermal conductivity. Over time, in

I, the process of destruction of the foam glass poisonous and unpleasant odors gases go into the room.

Block foam glass is also obtained by mixing finely ground glass with a foaming agent containing hydrates or carbonates of salts selected so that their dehydration or evolution of CO ₂ occurs at a temperature higher than the temperature of the transformation of the glass powder into a melt, which also allows the formation of bubbles that remain in the glass when it cools. A known method (US patent 5516351, POPs 19/06 from 05/14/1996) to obtain block foam glass from milled in a mill crushed glass and foaming agent CaCO3 or CaSO _{4 of a} given particle size distribution. They fill out forms, displace air from the mixture by blowing it with SO _x and / or CO _x gases and heat it up to the foaming temperature, then cool it and anneal it. It is well known that the use of ingredients whose chemical reactions with glass are accompanied by gas evolution does not provide fine-porous foam glass with bubbles completely isolated from the external environment. Density, thermal insulation, mechanical and other properties of such materials quickly and severely degrade in a humid atmosphere. The use of SO _x and CO _x gases increases the cost of production, has adverse environmental consequences and requires high costs for the capture and processing of gaseous emissions, which are dangerous for personnel working with them and the environment.

There is a general understanding that the best results can be achieved when the structure consists of closed bubbles, which makes the product impermeable to water, other liquids, water vapor and gases. This is what they tried to achieve in the work presented in US patent 5516351, POPs 19/06 from 05/14/1996. According to US patent 2775524, CL. 106-40 from 12.25.1956 glass is crushed with specially prepared materials such as diatomite and silica with a specific surface area of more than 10 m / g, containing carbon in the amount of 5-50 mass parts per 100 parts, at the rate of 0.08-0.15% carbon by weight of the glass; heating to a temperature sufficient to soften and foaming glass; cooling and annealing.

The method is most effective when in gas formation in oxidation Reducing reactions with a carbon ingredient involve toxic oxides of arsenic, antimony, vanadium, molybdenum, tungsten, and are practically not suitable for producing block foam glass with a low bulk density when SO ₃ or SO ₂ acts as an oxidizing agent.

Studies conducted in the work protected by patent RU 2187473 C2 indicate that it is possible to use recyclable glass residues to obtain an effective heat-insulating material with a low bulk density and closed bubbles only by adding them to specially welded glass with various foaming additives under the mandatory condition of introduction into the composition poisonous oxidizing agents SO ₃ , As ₂ Oz, Sb ₂ O _3, or combinations thereof.

Close to the claimed method is US patent 3151966, cl. 65-22, dated 10/06/1964, according to which foam glass is made by blowing gas through a molten glass melt with gas dissolving in the glass, introducing into the glass substances capable of forming gas bubbles in the melt, and substances that cause glass crystallization; the melt is cooled so that the bubbles formed during the extrusion of gas from the resulting crystals are retained in the cooled glass. The method considered here does not solve the problem of manufacturing foam glass without any pores, both immediately after manufacture and in the long term.

In all the methods of manufacturing foam glass used so far, the gas pressure in the bubbles during glass melting is significantly higher than atmospheric. At first, after cooling to ambient temperature, the pressure may be slightly lower than atmospheric, however, as permeable pores form in the walls of the bubbles, the gas pressure inside is usually compared with atmospheric. Thermal conductivity due to heat transfer by gas between the walls of the bubbles does not depend on pressure, while the diameter of the bubbles is greater than the mean free path of the molecules - about 50 nm under normal conditions. (I.V. Saveliev. Course in General Physics. T. 1. M.: Nauka, 1968. - S. 297-300).

The main reason for the formation of holes in the walls of the bubbles is the choice of foam glass manufacturing technologies, in which bubbles with too thin walls (1-10 microns thick) are formed and additives are used (crystallizers or foaming agents), which are incorporated into the composition of the walls of the bubbles during the production of foam glass and are gradually destroyed by atmospheric water, creating a system permeable to air and able to accumulate water from the atmosphere. With repeated cycles of freezing and thawing over several years, the foam glass gradually breaks down with ice crystals formed inside the bubbles. After analyzing the literature and many patents, we found that the most advanced technologies proposed only reduce the number of open pores, but do not allow glass to be completely pore-free, or with bubbles that remain closed for a long time under changing external conditions and such influences as numerous cycles freezing - thawing or boiling-cooling. In all the descriptions of the production of foam glass that we discovered, a mixture of glass powders and foaming agents was used, which did not allow the formation of too thin bubble walls. Moreover, the achievement of a minimum wall thickness is often considered desirable and, as a result, usually the wall thickness is 1-10 microns.

Usually, with further heating of the molten glass, gases are formed that were previously bound in the foaming agent, which turn the glass into foam glass. With a decrease in temperature, the reverse reactions of gas binding with highly reactive substances contained in the walls of the bubbles begin; during these chemical reactions, molecules capable of crystallization are formed, growing not only at high temperatures, while the glass is still viscous, but also (at a lower speed) during annealing and at room temperature. Mechanical stresses arising in the process of crystal growth contribute to damage to too thin walls; therefore, we consider an increase in the wall thickness of bubbles to be a necessary condition for the creation of foam glass with stable parameters.

Closest to the claimed method is a description of the production of foam glass in factories in the "Directory of a young worker for the production and processing of glass and glassware" / Guloyan Yu. A., Golozubov O. A. - M.: Vyssh. school., 1989. - S. 64. Table 45 gives a description of the methods of forming glass and among them are mentioned:

“Method: Foaming of glass melt under the influence of gases and the formation of foamy material of a certain shape uniformly penetrated by pores.

Characteristic: The molten glass melt is foamed in a vessel with multi-jet transmission of air or other gases through the thickness of the glass melt.

Produced glassware: Lightweight porous formless material (foam glass gravel and chips), porous lightweight slabs and blocks obtained by casting. "

Closest to the claimed method is also a description of the production of foam plastic in the Bulletin of the Center IKS APK APK - Issue. 2 (2001) (also published at http://www.ftcntr.ru/Bulltn/2001-02/13-kin.htm). Urea-formaldehyde foam is obtained by physically foaming the starting components with compressed air while observing their accurate dosing in accordance with the accepted production flow chart. Depending on the purpose, it is possible to obtain a foam with desired properties, for example, density, from 7 to 45 kg / m. CF-foam belongs to the group of hardly flammable materials. When heated above 300 ° C and exposed to an open flame, it does not burn and charred, decreasing in volume by 70-100 times, without emitting toxic substances. KF-foam does not mold, is resistant to organic solvents, is not destroyed by acids and alkalis. In the air-dry state, this polymer material has a cellular structure, consisting of 30-40% of closed pores and 60-70% of open pores, which determines its some breathability and water absorption. In water KF-foam does not swell and does not dissolve. The long list of permitted and recommended uses of CF-foam does not indicate housing construction, which is probably due to the possible slow release of hazardous decomposition products.

We note that the foamy materials obtained in this way have bubbles filled with gases, unlike those we offer, with bubbles practically without gas inside, and, therefore, having ten times lower thermal conductivity.

The purpose of our invention is to obtain foam materials from any glass and plastics separately and in the form of welded compositions having improved performance characteristics: bulk density of 0.1-0.45 g / cm ³ ; the gas pressure in the bubbles is less than 1 Pa and, as a result, the thermal conductivity is much lower than 0.06 W / (m ° C), achieved in gas-filled foam glasses. Our material does not absorb water even after numerous cycles of freezing-thawing or boiling-cooling; does not require subsequent machining; maintains small bends; passes a lot of light for use in light-scattering windows and hotbeds while simultaneously insulating the rooms.

This goal is achieved by the fact that in the known method for producing foam glass uniformly penetrated by pores, molten glass containing highly hygroscopic substances used for gas dehydration (anhydrous

CaO, BaO and Al ₂ O ₃ are part of various glasses in sufficient quantities) degassed and dehydrated by exposure at a temperature of 1450 ⁰ C for 10-60 minutes. Then the melt is cooled to 950-1200 ⁰ C and superheated steam is passed through it at a temperature of 950-1200 ⁰ C, obtained from degassed water or other substances capable of adsorbing in the walls at the temperature of the likely use of the material, turning into hydrates of salts, liquid or solid with vapor pressure in closed bubbles less than 1 Pa, at which the mean free path of molecules is much greater than the diameter of the bubbles 1-5 mm, and the thermal conductivity decreases in proportion to the vapor pressure, and heat insulating and sound insulating properties Twa are improving.

Similarly, CaO, BaO or AI ₂ O ₃ powders, degassed and dehydrated at a temperature of 1450 ^° C for 10-60 minutes, are added to the molten plastics and foamed with water vapor with a temperature of less than 200 ^° C obtained from degassed water so that closed bubbles with sufficiently strong walls capable of retaining bubbles after pressure drop below 1 Pa.

Bubbles in the melt, filled only with the indicated pairs, are crushed by mechanical devices, glass or plastic foam is squeezed into molds, from which hardened blocks are then taken out and placed in a thermal insulation cabinet for annealing by slow cooling. While in all descriptions of foam glass that we studied, wall thicknesses of 1–10 μm are considered permissible, we propose creating foam glass with bubble wall thicknesses from 0.05 mm to 1 mm. From the descriptions of the processes of structural and chemical transformations taking place in glass, it follows that in the thicker walls of the bubbles we propose, self-destruction of foam glass and pore formation will occur much more slowly, which will lead to a multiple increase in service life. Below temperature 2O ⁰ C, recommended for residential premises, there is a sharp decrease in water vapor pressure in the bubbles to 500-1000 Pa, but the thermal conductivity does not depend on the vapor pressure until it decreases to values at which the mean free path of the molecules exceeds the diameter of the bubbles. Under normal conditions, the mean free path of single water molecules is close to 50 nm; therefore, to ensure a mean free path of more than 5 mm (maximum bubble diameter), it is necessary to lower the pressure by a factor of 100,000, i.e., the pressure should be less than 1 Pa. Only at such a low pressure will the sound permeability and heat-insulating properties of the proposed foam material be better than for gas-filled foam materials. The composition of ordinary glasses for different purposes often includes 1-7% of very hygroscopic substances CaO, AI ₂ O ₃ and BaO, which is enough to reduce the water vapor pressure to 0.37 Pa in the case of CaO, 0.126 Pa in the case of Al ₂ O ₃ and up to 0.088 Pa in the case of BaO. (Handbook of analytical chemistry. - M.: Goskhimizdat, 1962. - P. 214). The mean free path of water molecules in this case will be, respectively, about 14 mm, 40 mm and 57 mm. Therefore, it is possible to reduce the thermal conductivity in bubbles with an average diameter of 2 mm by about 7, 20, and 28 times, respectively. In our foam glass, the pressure of superheated water vapor in impermeable bubbles will slightly exceed atmospheric pressure at a glass solidification temperature of about 700 ° C. If the foamglass cooling from 1200 ° C to 700 ° C is carried out rather quickly, then only part of the walls of the CaO, BaO, and Al ₂ O ₃ bubbles will bind a part of the water vapor. It is possible to ensure the binding of water residues with hygroscopic substances by setting a sufficiently long time for glass annealing at 450-600 ⁰ C, when the walls of the bubbles are hard enough to prevent the bubbles from shrinking, but they are still easily permeable to water vapor. Recrystallization of water-binding CaO, BaO, and Al ₂ O3 molecules in the bulk occurring at such temperatures glass walls of the bubbles will not destroy the walls of the bubbles due to their increased thickness and sufficient ductility. As a result, over decades the pressure of water vapor in the bubbles will be significantly lower than 1 Pa due to the binding of water with highly hygroscopic molecules in the depths of the walls of the bubbles; the mean free path of molecules will always be larger than the diameter of the bubbles and thermal conductivity over the entire service life will be significantly lower than that of foam glass made using existing technologies. When frozen, water bound to the wall molecules will not crystallize and damage the glass.

The heating rate to the melting point of glass or foam can be increased by preliminary grinding of raw materials, but in some cases it is permissible to throw pieces of glass or plastics of any size into the melt. One should only avoid trapping air or gases in the melt, which, when they get into the bubbles of foamy material, will remain gases at the temperature of the likely use of the material and will not allow to reduce the pressure in the bubbles after cooling to a level that is achievable when the bubbles are inflated only with superheated steam of degassed water or other substances having low vapor pressure at use temperatures. Additional glass degassing and dehydration of CaO ₅ BaO and Al ₂ O before foaming is provided by heating the glass to 145O ⁰ C and holding it at this temperature for 10-60 minutes. To increase the temperature, air enriched with oxygen and heated in the heat exchanger with smoke from the furnace can be fed into the furnace.

Since molten glass is chemically aggressive, to increase the service life of the equipment, it is recommended to cover the walls of the furnace, crucibles, and mechanical devices used to grind the bubbles with refractory glass. Foamy material is squeezed into molds coated with substances, preventing it from sticking to the walls of the mold (in particular, river or mountain sand, ash, chalk, soot, graphite or substances melting at a temperature below the pour point of foamy material, including tin, kick, lead or low-melting alloys), they are removed from the molds immediately after the blocks solidify (but until foamy material sticks to the walls of the mold) and anneal by smooth cooling in a heat-insulating cabinet (which can be made of foam glass). To prevent oxidation of the metal surfaces of the installation, oxygen should be removed from the gases entering the molds, for example, by feeding a mixture with a small excess of hydrogen or methane to the burners compared to oxygen.

To prevent damage to the foam glass during transportation, loading, unloading and installation, individual blocks of foam glass are connected into larger plates with thin sheets of foam plastic so that they are more flexible than foam glass; more resistant to external temperature and chemical influences than polystyrene plastic. At the same time, the thermal conductivity of composite panels at the junction of individual blocks is reduced, and foam glass protects the room from hazardous decomposition products of plastics.

The transparency, color of the foam glass, the number of bubbles formed and the thickness of their walls, the structural and mechanical properties of the blocks are determined by the purpose of the application - for thermal insulation, sound insulation, the manufacture of light-transmitting windows, structural material, architectural decorations, etc.

The proposed technical solution has a novelty, inventive step and is applicable both in large-scale industry and in small-scale production.

The inventive method can be processed into high-quality foam glass and foams with improved performance any types of glasses and plastics without preliminary grinding and without the introduction of foaming additives.

In order to develop the method, a wide range of glass and empty plastic bottles were successfully used as the starting material.

The examples below for the manufacture of foam glass are applicable for the manufacture of foam plastic, if you change the heating method and the applicable temperature specific for each grade and type of plastic.

FIG. 1. Methane or hydrogen is supplied to burner 1 with air or oxygen, heated by smoke leaving the furnace. The flame of the burner 1 melts the upper layers of glass 2 in the crucible bath 3, including glass adhering to the rotating roller 4. Through the tube 5 into the roller 4 with holes of various diameters on the surface superheated water vapor is supplied at a temperature of 950-1200 ° C, obtained from degassed water. The pressure should be sufficient to blow simultaneously many bubbles of different diameters in the molten glass.

To prevent oxidation of the plant parts, the oxygen in the furnace is burned completely due to a certain excess of combustible gas. A steel scraper 6, covered with a fusible substance, cuts off glass bubbles 7 inflated with water vapor from the surface of the roller 4 and directs them to a steel box (mold) 8 heated to 800 ° C, the walls of which are covered with a fusible substance. After filling with foam glass, the mold moves through a temporary airlock to the tunnel, the walls of which are made of foam glass and in which the temperature is maintained at 450-600 ° C. The length of the tunnel is chosen so that the cooling of blocks below 450-600 ^Q C occurs slowly enough to prevent the development of internal stresses in the foam glass and to facilitate the binding of water vapor with hygroscopic molecules in the walls of glass bubbles. Upon receipt of a new box with foamglass in the input gateway, all the boxes in the tunnel are shifted, and one of them is taken out of the output gateway. In this case, the temperature of the delivered box should be between the solidification temperature of the foam glass and the melting point of the substance on the walls of the box. In this case, it is possible to get the foam block out of the box without sticking to the walls and send for further smooth cooling to the second heat-insulated tunnel. After the foamglass block has completely cooled, residual adherents are removed from the surface using a suitable solvent.

FIG. 2. Similar to FIG. 1 with the difference that through additional tubes 9 water vapor is supplied into the molten glass at different speeds to facilitate the blowing of bubbles of various diameters necessary for the most dense filling of the foam glass with bubbles. Further, as in FIG. one.

FIG. 3. Similar to FIG. 2 with the difference that through the additional rotating tubes 9 with water holes displaced relative to the axis of rotation, water vapor is supplied to the glass melt. In this case, different tubes rotate at different speeds to facilitate the blowing of bubbles of different diameters, necessary for the most dense filling of the foam glass with bubbles.

FIG. 4. Superheated water vapor through the tube 5 is fed into a closed insulated box 3 at a glass melting point of 950-1200 ° C. Part of the steam 9 passes through a box with glass 2, melts the glass and exits through an adjustable valve 4. Another part of the steam simultaneously blows a lot of bubbles of different diameters in the molten glass 2, which are pressed through holes in the plate 1. Steel scraper 6, coated with a low-melting substance, cuts off blown glass bubbles 7 from the surface of the plate and directs them to a steel box (mold) 8 heated to 800 ° C, the walls of which are covered with a fusible substance. Further, as in FIG. one.

Claims

FORMULA OF THE INVENTION "METHOD FOR PRODUCING LONG-LASTING WATERPROOF FOAM GLASS AND REINFORCEMENTMACC"

1. A method of manufacturing foamy materials (namely, foam glass or foam plastic), comprising passing gas through a melt, characterized in that pieces of glass or plastics of any size are melted with the addition of very hygroscopic substances (for example, 1-7% anhydrous CaO, BaO or Al ₂ O ₃ are part of many glasses), the melt is degassed and dehydrated by exposure at a temperature of 1450 ° C for 10-60 minutes, the melt is cooled to 950-1200 ⁰ C, steam with a temperature of less than 200 ° C is passed through the melt in the case of plastics or superheated steam at a temperature of 950-1200 ⁰ C in cases glass obtained from degassed water or other substances capable of adsorbing in walls at the temperature of the likely use of the material, turn into salt hydrates, liquid or solid with vapor pressure in closed bubbles less than 1 Pa, at which the mean free path of the molecules is much greater than the diameter of the bubbles 1 -5 mm, and the thermal conductivity of a rarefied gas or vapor in the bubbles of the foamy material decreases with its pressure in the closed bubbles, the bubbles formed in the melt are mechanically crushed devices up to a diameter of 1-5 mm with a wall thickness of 0.05-1 mm, the foam material is squeezed into molds coated with substances that prevent it from sticking to the mold walls (in particular, river or mountain sand, ash, chalk, soot, graphite or substances melting at a temperature below the pour point of foamy materials, including tin, zinc, lead or low-melting alloys), are removed from the molds immediately after the blocks solidify (but until foamy materials adhere to the walls of the mold) and ι are annealed by smoothly refrigeration in a thermal insulation cabinet.

2. The method according to p. 1, characterized in that the relatively small blocks of foam glass and foam sheets made according to p. external temperature and chemical influences than foam.