CA2046508C - Process for the regeneration of used foundry sand - Google Patents
Process for the regeneration of used foundry sandInfo
- Publication number
- CA2046508C CA2046508C CA 2046508 CA2046508A CA2046508C CA 2046508 C CA2046508 C CA 2046508C CA 2046508 CA2046508 CA 2046508 CA 2046508 A CA2046508 A CA 2046508A CA 2046508 C CA2046508 C CA 2046508C
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- Canada
- Prior art keywords
- sand
- process according
- fluidized bed
- water
- organic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000004576 sand Substances 0.000 title claims abstract description 105
- 238000000034 method Methods 0.000 title claims abstract description 51
- 230000008569 process Effects 0.000 title claims abstract description 49
- 230000008929 regeneration Effects 0.000 title claims abstract description 8
- 238000011069 regeneration method Methods 0.000 title claims abstract description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 35
- 239000007767 bonding agent Substances 0.000 claims abstract description 16
- 239000003110 molding sand Substances 0.000 claims abstract description 7
- 239000000440 bentonite Substances 0.000 claims abstract description 5
- 229910000278 bentonite Inorganic materials 0.000 claims abstract description 5
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000012778 molding material Substances 0.000 claims abstract description 4
- 239000007849 furan resin Substances 0.000 claims abstract description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000005011 phenolic resin Substances 0.000 claims abstract description 3
- 239000011230 binding agent Substances 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 239000011148 porous material Substances 0.000 claims description 5
- 239000000446 fuel Substances 0.000 claims description 4
- 239000010802 sludge Substances 0.000 claims description 4
- 239000013505 freshwater Substances 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 2
- 238000007599 discharging Methods 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims 1
- 229910001413 alkali metal ion Inorganic materials 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 239000003638 chemical reducing agent Substances 0.000 claims 1
- 238000005470 impregnation Methods 0.000 claims 1
- 238000004140 cleaning Methods 0.000 description 9
- 235000012239 silicon dioxide Nutrition 0.000 description 6
- 239000010453 quartz Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 238000002791 soaking Methods 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000428 dust Substances 0.000 description 3
- 230000001172 regenerating effect Effects 0.000 description 3
- 238000009736 wetting Methods 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000005194 fractionation Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000002918 waste heat Substances 0.000 description 2
- 101100000858 Caenorhabditis elegans act-3 gene Proteins 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000004035 construction material Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000005202 decontamination Methods 0.000 description 1
- 230000003588 decontaminative effect Effects 0.000 description 1
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- -1 for example Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000007885 magnetic separation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910052863 mullite Inorganic materials 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000004707 phenolate Chemical class 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 230000000930 thermomechanical effect Effects 0.000 description 1
Landscapes
- Molds, Cores, And Manufacturing Methods Thereof (AREA)
- Mold Materials And Core Materials (AREA)
Abstract
A process is disclosed for the regeneration of used foundry sand, whose original molding sand contained as molding material inorganic bonding agents such as bentonite (= "inorganic used sand") and/or organic bonding agents such as phenolic and/or furan resins (= "organic used sand"). The used sand to-be-cleaned is soaked with water and subsequently moved into a heated fluidizing bed in its wet condition.
Description
2U46~08 This invention relates to a process for the regeneration of used foundry sand whose original molding sand contains as molding material inorganic bonding agents such as bentonite (= "inorganic used sand") and/or organic bonding agents such as, for example, phenolic and/or furan resins (= "organic used sand").
In inorganically bonded molding sands the bonding agent bentonite or a similar material is fixed in shell-form at the surface of the sand grains by oolithization, depending on the degree of heat treatment during casting, while molding sands with organic bonding agents suffer thermal decomposition during casting and thus acquire at the grain surface firmly adhering residues of carbon-rich derivatives from the organic bonding agents. In addition, the used sand is further contaminated because of additional additives, such as the formation of lustrous carbons from the additives.
While used (foundry) sand was formerly at least predominantly simply disposed of, acute scarcity of available deposit sites and also cost considerations today have led to a demand for the regeneration, i.e. cleaning, of used sand, so that it may be re-used. However, this requires that the above-mentioned bonding agent shells and other contaminations of the used sand be separated from the quartz bodies and then eliminated.
A known method of regenerating used foundry sand which consists at least predominately of organic used sand is to treat it thermally by annealing at a temperature of ca. 800 degrees C and/or possibly pneumatically. In this process the bonding agent shells and other contaminations of the used sand are generally so thoroughly removed that the used sand can be reused as molding sand. On the other hand, this thermal cleaning process does not give rise to satisfactory results with inorganic used sands.
The thermo-mechanical process known from German Patent No. 31 03 030 has useful results only if the --- 2~!~6~8 proportion of inorganic sand is relatively small.
Consequently, this process does not solve the above problem, since used foundry sand generally consists of more than two thirds of inorganic used sand.
In view of these conditions, German Patent No. 38 15 877 has proposed (e.g. according to German Patent No. 31 03 030) that the thermo-mechanically pre-treated or treated regenerate be subsequently treated ultrasonically in water (as a coupling layer). In this way the bonding agent shells, which are sintered onto the sand grains, are caused to split off and the degree of oolithization is lowered to normal values, while simultaneously the basic pH value of the regenerate is adjusted to a near neutral value.
Quite apart from the complex and costly equipment needed for implementing the above process, as well as the high operating costs, further costs arise because the cleaned sand still has to be dried, which makes this multi-step process very uneconomical. In addition, it should be noted that, due to a relatively high wear factor for the sand grains, only a relatively low regenerate yield of sufficient quality can be achieved.
For the regeneration of used inorganic sand processes have been developed in which it was attempted to remove the bonding agent shells by a wet process from the surface of the sand grains. This was accomplished by means of mechanical stirring in a watery sand suspension resulting in intensive friction among the sand grains.
This process step, which is also called attrition, is generally repeated several times and possibly affected or intensified by creating special sand-water-mix conditions (see e.g. U.S. Patent No. 27 83 511 or German OLS 30 19 096).
One disadvantage of this wet process is the fact that hydrocarbon compounds of organic used sand portions, as well as lustrous carbons and their generating agents, cannot be sufficiently removed. These materials act - 3 20465~ 8 practically as lubricants (as, e.g. argillaceous components) and prevent the desired abrasion, so that sufficiently satisfactory regenerating results cannot be obtained even with multi-step attrition.
In order to solve this problem, Australian Patent No. 387 921 suggested conducting a sludge removal (by means of classifiers) after each attrition step, so that the "lubricants" are thus removed from the circulating water and the desired abrasion is intensified. However, even if a satisfactory result could be obtained from a technical point of view with three-, four- or manifold attrition, this result would be considerably burdened with the attendant costs. In addition, in this process an adherent structure of finely distributed, porous silicic acid remains on the grain surface, which necessitates increased amounts of bonding agents when the cleaned used sand is reused as new foundry sand.
It is an object of the present invention, while avoiding the above-mentioned and other disadvantages, to create a process for the cleaning of used foundry sand which is satisfactory both from a technical and an economical point of view, in which process (as compared with the state of the art) a relatively low technical and financial effort produces a regenerated material which is extensively and generally usable and which contains relatively few harmful components, and can be reused without problems in place of new sand for mold and core production in foundries.
Accordingly, the present invention provides a process for the regeneration of used organic or inorganic foundry sand formed from original molding sand which contained, as the molding material, inorganic binders in the case of inorganic used sand or organic binders in the case of organic used sand, said binders being fixed in a shell form at the surface of the sand grains of said used sand, said process comprising the steps of:
, ~
In inorganically bonded molding sands the bonding agent bentonite or a similar material is fixed in shell-form at the surface of the sand grains by oolithization, depending on the degree of heat treatment during casting, while molding sands with organic bonding agents suffer thermal decomposition during casting and thus acquire at the grain surface firmly adhering residues of carbon-rich derivatives from the organic bonding agents. In addition, the used sand is further contaminated because of additional additives, such as the formation of lustrous carbons from the additives.
While used (foundry) sand was formerly at least predominantly simply disposed of, acute scarcity of available deposit sites and also cost considerations today have led to a demand for the regeneration, i.e. cleaning, of used sand, so that it may be re-used. However, this requires that the above-mentioned bonding agent shells and other contaminations of the used sand be separated from the quartz bodies and then eliminated.
A known method of regenerating used foundry sand which consists at least predominately of organic used sand is to treat it thermally by annealing at a temperature of ca. 800 degrees C and/or possibly pneumatically. In this process the bonding agent shells and other contaminations of the used sand are generally so thoroughly removed that the used sand can be reused as molding sand. On the other hand, this thermal cleaning process does not give rise to satisfactory results with inorganic used sands.
The thermo-mechanical process known from German Patent No. 31 03 030 has useful results only if the --- 2~!~6~8 proportion of inorganic sand is relatively small.
Consequently, this process does not solve the above problem, since used foundry sand generally consists of more than two thirds of inorganic used sand.
In view of these conditions, German Patent No. 38 15 877 has proposed (e.g. according to German Patent No. 31 03 030) that the thermo-mechanically pre-treated or treated regenerate be subsequently treated ultrasonically in water (as a coupling layer). In this way the bonding agent shells, which are sintered onto the sand grains, are caused to split off and the degree of oolithization is lowered to normal values, while simultaneously the basic pH value of the regenerate is adjusted to a near neutral value.
Quite apart from the complex and costly equipment needed for implementing the above process, as well as the high operating costs, further costs arise because the cleaned sand still has to be dried, which makes this multi-step process very uneconomical. In addition, it should be noted that, due to a relatively high wear factor for the sand grains, only a relatively low regenerate yield of sufficient quality can be achieved.
For the regeneration of used inorganic sand processes have been developed in which it was attempted to remove the bonding agent shells by a wet process from the surface of the sand grains. This was accomplished by means of mechanical stirring in a watery sand suspension resulting in intensive friction among the sand grains.
This process step, which is also called attrition, is generally repeated several times and possibly affected or intensified by creating special sand-water-mix conditions (see e.g. U.S. Patent No. 27 83 511 or German OLS 30 19 096).
One disadvantage of this wet process is the fact that hydrocarbon compounds of organic used sand portions, as well as lustrous carbons and their generating agents, cannot be sufficiently removed. These materials act - 3 20465~ 8 practically as lubricants (as, e.g. argillaceous components) and prevent the desired abrasion, so that sufficiently satisfactory regenerating results cannot be obtained even with multi-step attrition.
In order to solve this problem, Australian Patent No. 387 921 suggested conducting a sludge removal (by means of classifiers) after each attrition step, so that the "lubricants" are thus removed from the circulating water and the desired abrasion is intensified. However, even if a satisfactory result could be obtained from a technical point of view with three-, four- or manifold attrition, this result would be considerably burdened with the attendant costs. In addition, in this process an adherent structure of finely distributed, porous silicic acid remains on the grain surface, which necessitates increased amounts of bonding agents when the cleaned used sand is reused as new foundry sand.
It is an object of the present invention, while avoiding the above-mentioned and other disadvantages, to create a process for the cleaning of used foundry sand which is satisfactory both from a technical and an economical point of view, in which process (as compared with the state of the art) a relatively low technical and financial effort produces a regenerated material which is extensively and generally usable and which contains relatively few harmful components, and can be reused without problems in place of new sand for mold and core production in foundries.
Accordingly, the present invention provides a process for the regeneration of used organic or inorganic foundry sand formed from original molding sand which contained, as the molding material, inorganic binders in the case of inorganic used sand or organic binders in the case of organic used sand, said binders being fixed in a shell form at the surface of the sand grains of said used sand, said process comprising the steps of:
, ~
2 ~ 8 a) impregnating the used sand to be reconditioned with water to such an extent to substantially fill the pores of the grain shells of the sand with water;
b) providing a heated fluidized bed consisting of sand;
c) maintaining said fluidized bed at a steady temperature of about 750 to 950~C;
d) feeding said used sand impregnated with water into the heated fluidized bed; and e) discharging the sand from said fluidized bed.
-- 20~6~08 Thus, the used sand to-be-cleaned is (to begin with) soaked in water and then placed in its wet condition into the heated fluidized bed, where the shock-heating of the used sand causes a spontaneous evaporation of the water located in the pores thereof. The resulting considerable increase in volume causes the shells (at least) of the (inorganic) bonding agent to split off or at least to be loosened to an extent that they can be directly separated from the quartz grains in the fluidized bed. the traditional drying of wet-regenerated used sand by hot air at temperatures of ca. 150-300 degrees C in various devices does not achieve such a splitting-off or loosening effect, as is proven by the above-mentioned bonding agent requirements.
The heat removal by water evaporation in the immediate proximity of the quartz grains also prevents possible changes of crystal modification and/or grain decomposition, due to the shock-like heating of the quartz grains. In addition, the sintering onto the grain surface of mullite, which has been created from bentonite due to the effect of heat, is prevented or at least inhibited.
Furthermore, it is not necessary in the process of the invention that the used sand, which may consist of any mixture of organically and inorganically bonded used sands, must during wetting or soaking pass through an attrition step which is otherwise required for wet regeneration. The simplified operation and the less costly equipment result in considerable economic advantages.
Consequently, it is not at all necessary in the process of the invention (even though it may be practical in certain cases) to assure a basic separation of organic and inorganic used sand in the preparatory stages of the cleaning, while it is indeed practical to clean the organic and inorganic used sand essentially separately from one another if they are not already separate, as this is often the case.
20~6~ ~8 Furthermore, it is advantageous that practically no harmful residues occur, that in accordance with the above explanations it is not necessary to maintain a certain proportion of different used sands for cleaning, and that quite clearly no separate process branches are required and have to be adjusted to one another, which, as is well known, can generally cause considerable difficulties especially in a hot process.
As a rule it has proved to be highly practical to soak the used sand so thoroughly with water (while the water may be given additives for lowering surface tension) that the pores located between the grain shells are at least essentially filled with water in order to optimize the above-mentioned effect and, in the final analysis, to optimize the entire used sand cleaning process and the quality of the regenerate.
In a preferred embodiment of the invention the soaking of the used sand is carried out with circulated water in order to eliminate harmful components, especially alkalis. This operating method is practical in cases where the used sand contains, as a result of the use of alkali-silicates or phenolates as bonding components, significant amounts of such ions. If these were allowed to remain in the sand regenerate, the resulting high basicity would significantly limit reusability.
If necessary, the water used for soaking the used sand may be kept at a pH value between 2 and 5 by continuous addition of acid and is kept in circulation until a maximum salt concentration (to be determined in each case) has been reached. Furthermore, the exchange with fresh water may be carried out continuously. Before each entry into the soaking device the circulating water passes through a settling tank and, if necessary, a filter, where the solids absorbed by the water from the sand in the form of sludge can be separated and the sludge can be returned to the fluidized bed. The shock-like heating of 20~6508 these solids, which are continuously soaked with water, also prevents a sintering onto the sand grains, and their organic components burn out.
In another embodiment of this process variant, carbon dioxide is used as an anionic component of the decomposition of the alkali-silicates instead of mineral or carboxylic acid. Here the circulating water acquires a basic pH value; however, the alkalis are removed from the used sand just as well, namely in the form of carbonates.
The alkaline solution which still adheres to the used sand is rinsed from the grains by spraying on the drainage screen with the fresh water required as replacement. The resulting soda or potash solution can be evaporated with exhaust or waste heat, crystallized and the alkali can thus be recovered therefrom in a reusable form.
However, the process is extremely satisfactory not only from a technical, but also from an economical point of view, especially since the heated fluidized bed itself can consist of sand (even of already cleaned sand, if necessary).
In order to have available a fluidized bed with sufficient heating capacity to obtain the desired results, the ratio of the fluidized bed sand quantity to the amount of wet used sand which is added per minute should be in the range of about 50 to 100.
In accordance with the invention the fluidized bed is most preferably heated from the top, preferably with high-speed burners, for which gaseous fuels have proven to be especially practical as additional fuels (beyond fuel already contained in the used sand).
In order to obtain the above-explained effects, the fluidized bed is preferably maintained at a stable temperature in the range of about 750 to 950 degrees C.
According to a further preferred embodiment of the invention, the temperature in the solid material, on the one hand, and in the gas chamber above the fluidized -- 20~6508 bed, on the other, can be variably adjusted, as can the dwell time of the used sand in the fluidized bed, i.e.
depending on its composition.
In this manner complete burn-out of organic substances even in flying dust, and thus is decontamination, is achieved.
In order to intensify and/or accelerate the wetting of the used sand it can be advantageous if the used sand which is to be wetted and cleaned is wetted in a vacuum.
It is also quite practical as a rule if the propelling speed or velocity of the fluidized bed is adjustable over a wide range, so that the operating conditions can be optimally suited to the respective requirements of the used sand.
Furthermore, it can be practical to separate sand in a separator or similar device downstream of the fluidized bed, in which case it may be further practical to return this separated sand partially to the fluidized bed.
The used sand (regenerate) cleaned in this manner can be subjected to subsequent mechanical cleaning if desired.
A preferred embodiment of the invention will now be described with reference to the accompanying drawing which illustrates diagrammatically an apparatus for carrying out the process for regenerating used foundry sand.
The drawing shows as a diagrammatic representation a bin 1, in which the used sand (which is routinely a mixture of inorganic and organic used sand) is collected. The used sand to-be-cleaned is moved from the bin 1 into used sand pre-treatment equipment 2, consisting of for example means for magnetic separation of Fe particles, a lump crusher and a sifter, and is then moved into an intermediate bin 3.
2o~6so8 -From the intermediate bin 3 the pre-treated used sand is filled into a mixer 5 by means of a dosing device 4. Into this mixer 5 are added dosed water from a dosing device 6 and materials for the reduction of surface tension. The water is heated to a maximum of 95 degrees C
with exhaust or waste heat.
The wet sand is rotated in a conditioner 7 until complete wetting of the pores of the grain shells is attained and then reaches a fluidized bed oven 8 in dosed form.
As a result of the extremely fast heat transfer (and the good mixing in the fluidized bed) the wet used sand is heated abruptly to an operating temperature of 800 to 850 degrees C, while the above-described formation of steam splits the fire-clay shells off the (quartz) sand grains, or at least loosens them considerably, and harmful organic materials burn off completely. The separated shells are trapped in a separator 9.
The oven exhaust gas is cooled in a heat exchanger 11 by preheating the fluidizing air and then passes through a filter 10.
To cool the oven discharge the latter first passes through a fluidizing bed cooler 12, in which the water needed for soaking is pre-heated to 70 to 95 degrees C and the perceptible heat of the sand is recovered in the form of steam or hot water.
A concluding treatment of the resulting regenerate occurs in a pneumatic cleaning device 13 and by fractionation into (at least) two grain sizes ("coarse" and "fine"). The cleaned used sand is universally reusable, while the granulating of the new sand which is to be formed from the cleaned used sand (if necessary by adding certain amounts of new sand) can be achieved by dosing from the various fractionations in order to obtain used sand with pre-determined average granulation or a certain grain bond.
After cooling and pneumatic cleaning of the 2Q~650~
treated sand, regenerate and filter dust are obtained. The filter dust is free of harmful substances and may be disposed of or used as construction material or additive without any problem.
b) providing a heated fluidized bed consisting of sand;
c) maintaining said fluidized bed at a steady temperature of about 750 to 950~C;
d) feeding said used sand impregnated with water into the heated fluidized bed; and e) discharging the sand from said fluidized bed.
-- 20~6~08 Thus, the used sand to-be-cleaned is (to begin with) soaked in water and then placed in its wet condition into the heated fluidized bed, where the shock-heating of the used sand causes a spontaneous evaporation of the water located in the pores thereof. The resulting considerable increase in volume causes the shells (at least) of the (inorganic) bonding agent to split off or at least to be loosened to an extent that they can be directly separated from the quartz grains in the fluidized bed. the traditional drying of wet-regenerated used sand by hot air at temperatures of ca. 150-300 degrees C in various devices does not achieve such a splitting-off or loosening effect, as is proven by the above-mentioned bonding agent requirements.
The heat removal by water evaporation in the immediate proximity of the quartz grains also prevents possible changes of crystal modification and/or grain decomposition, due to the shock-like heating of the quartz grains. In addition, the sintering onto the grain surface of mullite, which has been created from bentonite due to the effect of heat, is prevented or at least inhibited.
Furthermore, it is not necessary in the process of the invention that the used sand, which may consist of any mixture of organically and inorganically bonded used sands, must during wetting or soaking pass through an attrition step which is otherwise required for wet regeneration. The simplified operation and the less costly equipment result in considerable economic advantages.
Consequently, it is not at all necessary in the process of the invention (even though it may be practical in certain cases) to assure a basic separation of organic and inorganic used sand in the preparatory stages of the cleaning, while it is indeed practical to clean the organic and inorganic used sand essentially separately from one another if they are not already separate, as this is often the case.
20~6~ ~8 Furthermore, it is advantageous that practically no harmful residues occur, that in accordance with the above explanations it is not necessary to maintain a certain proportion of different used sands for cleaning, and that quite clearly no separate process branches are required and have to be adjusted to one another, which, as is well known, can generally cause considerable difficulties especially in a hot process.
As a rule it has proved to be highly practical to soak the used sand so thoroughly with water (while the water may be given additives for lowering surface tension) that the pores located between the grain shells are at least essentially filled with water in order to optimize the above-mentioned effect and, in the final analysis, to optimize the entire used sand cleaning process and the quality of the regenerate.
In a preferred embodiment of the invention the soaking of the used sand is carried out with circulated water in order to eliminate harmful components, especially alkalis. This operating method is practical in cases where the used sand contains, as a result of the use of alkali-silicates or phenolates as bonding components, significant amounts of such ions. If these were allowed to remain in the sand regenerate, the resulting high basicity would significantly limit reusability.
If necessary, the water used for soaking the used sand may be kept at a pH value between 2 and 5 by continuous addition of acid and is kept in circulation until a maximum salt concentration (to be determined in each case) has been reached. Furthermore, the exchange with fresh water may be carried out continuously. Before each entry into the soaking device the circulating water passes through a settling tank and, if necessary, a filter, where the solids absorbed by the water from the sand in the form of sludge can be separated and the sludge can be returned to the fluidized bed. The shock-like heating of 20~6508 these solids, which are continuously soaked with water, also prevents a sintering onto the sand grains, and their organic components burn out.
In another embodiment of this process variant, carbon dioxide is used as an anionic component of the decomposition of the alkali-silicates instead of mineral or carboxylic acid. Here the circulating water acquires a basic pH value; however, the alkalis are removed from the used sand just as well, namely in the form of carbonates.
The alkaline solution which still adheres to the used sand is rinsed from the grains by spraying on the drainage screen with the fresh water required as replacement. The resulting soda or potash solution can be evaporated with exhaust or waste heat, crystallized and the alkali can thus be recovered therefrom in a reusable form.
However, the process is extremely satisfactory not only from a technical, but also from an economical point of view, especially since the heated fluidized bed itself can consist of sand (even of already cleaned sand, if necessary).
In order to have available a fluidized bed with sufficient heating capacity to obtain the desired results, the ratio of the fluidized bed sand quantity to the amount of wet used sand which is added per minute should be in the range of about 50 to 100.
In accordance with the invention the fluidized bed is most preferably heated from the top, preferably with high-speed burners, for which gaseous fuels have proven to be especially practical as additional fuels (beyond fuel already contained in the used sand).
In order to obtain the above-explained effects, the fluidized bed is preferably maintained at a stable temperature in the range of about 750 to 950 degrees C.
According to a further preferred embodiment of the invention, the temperature in the solid material, on the one hand, and in the gas chamber above the fluidized -- 20~6508 bed, on the other, can be variably adjusted, as can the dwell time of the used sand in the fluidized bed, i.e.
depending on its composition.
In this manner complete burn-out of organic substances even in flying dust, and thus is decontamination, is achieved.
In order to intensify and/or accelerate the wetting of the used sand it can be advantageous if the used sand which is to be wetted and cleaned is wetted in a vacuum.
It is also quite practical as a rule if the propelling speed or velocity of the fluidized bed is adjustable over a wide range, so that the operating conditions can be optimally suited to the respective requirements of the used sand.
Furthermore, it can be practical to separate sand in a separator or similar device downstream of the fluidized bed, in which case it may be further practical to return this separated sand partially to the fluidized bed.
The used sand (regenerate) cleaned in this manner can be subjected to subsequent mechanical cleaning if desired.
A preferred embodiment of the invention will now be described with reference to the accompanying drawing which illustrates diagrammatically an apparatus for carrying out the process for regenerating used foundry sand.
The drawing shows as a diagrammatic representation a bin 1, in which the used sand (which is routinely a mixture of inorganic and organic used sand) is collected. The used sand to-be-cleaned is moved from the bin 1 into used sand pre-treatment equipment 2, consisting of for example means for magnetic separation of Fe particles, a lump crusher and a sifter, and is then moved into an intermediate bin 3.
2o~6so8 -From the intermediate bin 3 the pre-treated used sand is filled into a mixer 5 by means of a dosing device 4. Into this mixer 5 are added dosed water from a dosing device 6 and materials for the reduction of surface tension. The water is heated to a maximum of 95 degrees C
with exhaust or waste heat.
The wet sand is rotated in a conditioner 7 until complete wetting of the pores of the grain shells is attained and then reaches a fluidized bed oven 8 in dosed form.
As a result of the extremely fast heat transfer (and the good mixing in the fluidized bed) the wet used sand is heated abruptly to an operating temperature of 800 to 850 degrees C, while the above-described formation of steam splits the fire-clay shells off the (quartz) sand grains, or at least loosens them considerably, and harmful organic materials burn off completely. The separated shells are trapped in a separator 9.
The oven exhaust gas is cooled in a heat exchanger 11 by preheating the fluidizing air and then passes through a filter 10.
To cool the oven discharge the latter first passes through a fluidizing bed cooler 12, in which the water needed for soaking is pre-heated to 70 to 95 degrees C and the perceptible heat of the sand is recovered in the form of steam or hot water.
A concluding treatment of the resulting regenerate occurs in a pneumatic cleaning device 13 and by fractionation into (at least) two grain sizes ("coarse" and "fine"). The cleaned used sand is universally reusable, while the granulating of the new sand which is to be formed from the cleaned used sand (if necessary by adding certain amounts of new sand) can be achieved by dosing from the various fractionations in order to obtain used sand with pre-determined average granulation or a certain grain bond.
After cooling and pneumatic cleaning of the 2Q~650~
treated sand, regenerate and filter dust are obtained. The filter dust is free of harmful substances and may be disposed of or used as construction material or additive without any problem.
Claims (24)
1. A process for the regeneration of used organic or inorganic foundry sand formed from original molding sand which contained, as the molding material, inorganic binders in the case of inorganic used sand or organic binders in the case of organic used sand, said binders being fixed in a shell form at the surface of the sand grains of said used sand, said process comprising the steps of:
a) impregnating the used sand to be reconditioned with water to such an extent to substantially fill the pores of the grain shells of the sand with water;
b) providing a heated fluidized bed consisting of sand;
c) maintaining said fluidized bed at a steady temperature of about 750 to 950°C;
d) feeding said used sand impregnated with water into the heated fluidized bed; and e) discharging the sand from said fluidized bed.
a) impregnating the used sand to be reconditioned with water to such an extent to substantially fill the pores of the grain shells of the sand with water;
b) providing a heated fluidized bed consisting of sand;
c) maintaining said fluidized bed at a steady temperature of about 750 to 950°C;
d) feeding said used sand impregnated with water into the heated fluidized bed; and e) discharging the sand from said fluidized bed.
2. A process according to Claim 1, wherein the water used for impregnating the used sand is circulated and harmful alkali metal ions are thereby dissolved out.
3. A process according to Claim 2, wherein said circulated water is maintained at a pH of between 2 and 5 by addition of mineral acids or carboxylic acids and is replaced by fresh water to such an extent that a salt concentration, which is to be pre-determined, in the circulated water is not exceeded.
4. A process according to Claim 2 or 3, wherein said circulated water is treated with CO2 in the alkaline range and the alkalis are thus recovered as carbonates.
5. A process according to Claim 2, 3, or 4, wherein said circulated water is purified and filtered and the sludge thus obtained is recycled into the fluidized bed.
6. A process according to Claim 1, 2, 3, 4 or 5, wherein the ratio of the rate of fluidized-bed sand to the rate of moist used sand fed per minute is about 50 to 100.
7. A process according to Claim 1, 2, 3, 4, 5 or 6, wherein inorganic and organic used sands in any desired mixtures with one another are impregnated with water and these mixtures are then fed to the fluidized bed.
8. A process according to Claim 1, wherein used sand with at least predominantly organic binders is introduced separately into the fluidized bed.
9. A process according to Claim 8, wherein only the inorganic used sand is impregnated with water.
10. A process according to Claim 8, wherein exclusively organic used sand is separately introduced into the fluidized bed which has been impregnated separately with water.
11. A process according to any one of Claims 1 to 10, wherein the water is preheated to 70 to 95°C.
12. A process according to Claim 9, wherein surface tension-reducing agents are added to said water.
13. A process according to any one of Claims 1 to 12, wherein the fluidized bed is heated from above.
14. A process according to Claim 13, wherein said heating from above is achieved by using a gaseous fuel.
15. A process according to any one of Claims 1 to 14, wherein the temperature in the fluidized bed and the temperature in the gas space above the fluidized bed are adjusted to different levels.
16. A process according to any one of Claims 1 to 15, wherein residence time of the used sand to be reconditioned in the fluidized bed is adjustable.
17. A process according to any one of Claims 1 to 16, wherein said impregnation is enhanced by means of a vacuum.
18. A process according to any one of Claims 1 to 17, wherein the fluidizing velocity of the fluidized bed is adjustable within wide limits.
19. A process according to any one of Claims 1 to 18, wherein sand, which has been precipitated in a separator or the like downstream of the fluidized bed, is partially recycled into the fluidized bed.
20. A process according to any one of Claims 1 to 19, wherein the regenerated used sand product is finally purified mechanically or pneumatically or mechanically/pneumatically.
21. A process according to any one of Claims 1 to 20, wherein fluidizing air is preheated by heat transfer from the exhaust gas from the fluidized bed.
22. A process according to any one of Claims 1 to 21, wherein heating is operated close to the stoichiometric fuel-air ratio.
23. A process according to any one of Claims 1 to 9, 11 to 22, wherein the original molding sand contained bentonite as an inorganic bonding agent.
24. A process according to any one of Claims 1 to 23, wherein the original molding sand contained a phenolic or furan resin or mixture thereof as an organic bonding agent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA 2046508 CA2046508C (en) | 1991-07-09 | 1991-07-09 | Process for the regeneration of used foundry sand |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA 2046508 CA2046508C (en) | 1991-07-09 | 1991-07-09 | Process for the regeneration of used foundry sand |
Publications (2)
Publication Number | Publication Date |
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CA2046508A1 CA2046508A1 (en) | 1993-01-10 |
CA2046508C true CA2046508C (en) | 1998-04-28 |
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ID=4147971
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CA 2046508 Expired - Fee Related CA2046508C (en) | 1991-07-09 | 1991-07-09 | Process for the regeneration of used foundry sand |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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CN109396328A (en) * | 2018-12-17 | 2019-03-01 | 合肥仁创铸造材料有限公司 | A kind of combining and regenerating technique and the inorganic reclaimed sand of inorganic old sand thermal method and wet process |
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CN114042860B (en) * | 2021-11-29 | 2024-02-09 | 金耐源(河南)工业科技有限公司 | Low-emission environment-friendly casting mold material recycling process |
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1991
- 1991-07-09 CA CA 2046508 patent/CA2046508C/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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CN109396328A (en) * | 2018-12-17 | 2019-03-01 | 合肥仁创铸造材料有限公司 | A kind of combining and regenerating technique and the inorganic reclaimed sand of inorganic old sand thermal method and wet process |
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CA2046508A1 (en) | 1993-01-10 |
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