Filter for holding and raising ground water

Details Filter for holding and raising ground water Filter for holding and raising ground water

1997-11-06

2002-04-16

Popovics, Robert J. (Department: 1723)

Liquid purification or separation

Filter

Supported, shaped or superimposed formed mediums

C210S502100, C210S503000, C210S506000

Reexamination Certificate

active

06372135

ABSTRACT:

BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to a filter of polyurethane-bonded solid layer of silica sand for holding and raising ground water, for treating industrial water and drinking water and for the infiltration of water into the ground and to the production and use of the filter in surface mining regions.
2. Discussion of Related Art
One such filter for surface mining regions is known from DD 109 319. This document describes a filter produced from dry granular components suitable as a filter material and a two-component polyurethane adhesive, the ratio by weight being at least 20:1. Gravel sand with a particle size of 1.6 to 3.5 mm is preferably used as the granular filter material. The mixture of the two constituents is preferably cured in the presence of a catalyst at temperatures not exceeding 120° C. The known filter has the disadvantage that it is not suitable for the production of drinking water because the filtrate foams and contains organically bound carbon in unacceptable quantities. In addition, dust-containing silica sand filters produced with a polyurethane adhesive without a modifying agent turn soft when stored in water.
In addition, European patent application 0 468 608 describes a drainage element of a mixture consisting of 20 to 30 parts by weight of dried filter gravel as aggregate and 1 part by weight of a polyurethane-based resin as binder. The dust in the filter gravel interferes with the production of the drainage elements. Where the unidentified polyurethane binder is used, the drainage element is difficult if not impossible to demold. The percentage of useable elements is very small. In addition, the concentration of binder distinctly increases in the downward direction in the individual elements. It is not possible to achieve uniform strength throughout the drainage element.
Accordingly, the problem addressed by the present invention was inexpensively to produce a filter with which ground water could be held, particularly in surface mining regions and used for the production of industrial water and drinking water. The filter would of course meet mechanical requirements which its intended application involves.
SUMMARY OF THE INVENTION
The solution provided by the invention is defined in the claims. It lies essentially in the use of a certain binder system based on a polyurethane adhesive. According to the characterizing clause, the binder contains an organotin compound with a molecular weight of more than 600 as catalyst and a mixture of highly dispersed silica and/or bentonite with a thickened aluminosilicate as modifier.
DETAILED DESCRIPTION OF THE INVENTION
In the context of the invention, the “polyurethane binder” is understood to be a adhesive binder consisting of polyisocyanates, polyols, catalysts, modifiers and fillers. A two-component polyurethane adhesive is preferably used, a low molecular weight polyisocyanate and a relatively low molecular weight polyol containing the other additives being mixed together shortly before the use of the adhesive.
PolyhydroxyPolyethers known per se with a molecular weight of 60 to 10,000 and preferably 70 to 6,000 containing 2 to 10 hydroxyl groups are particularly suitable for the production of the reactive isocyanate/polyol resin. Polydydroxypolyethers such as these are obtained in known manner by alkoxylation of suitable starter molecules, for example water, propylene glycol, ethylene glycol, glycerol, trimethylol propane. Suitable alkoxylating agents are, in particular, propylene oxide and even ethylene oxide.
Suitable polyisocyanates are any polyfunctional aromatic and aliphatic isocyanates. In a preferred embodiment, they contain an average of 2 to at most 4 NCO groups. Aromatic isocyanates are preferred, diphenyl methane diisocyanate being particularly preferred.
The polyols and polyisocyanates are preferably used as a two-component casting resin, a low molecular weight polyisocyanate and relatively low molecular weight polyol being mixed together just before the use of the resin. The polyisocyanate is used with an excess of isocyanate of up to 30%, based on the polyol, and preferably with an excess of 10 to 25%.
The “organotin compound” is understood to be a compound containing one or more Sn—C bonds. Specific compounds are dibutyl and dioctyl tin dilaurate, dioctyl tin di-2-ethylhexoate, dibutyl and dioctyl tin distearate, dibutyl and dioctyl tin didodecyl thiolate, butyl and octyl tin tris-(thioglycolic acid-2-ethylhexoate), dibutyl and dioctyl tin bis-(thioglycolic acid-2-ethylhexoate), tributyl and trioctyl tin (thioglycolic acid-2-ethylhexoate) and tributyl and trioctyl tin tris-(thioethyleneglycol-2-ethylhexoate), tributyl and trioctyl tin bis (thioethyleneglycol-2-ethylhexoate), tributyl and trioctyl tin (thioethyleneglycol-2-ethylhexoate) with the general formula R
n
Sn(S—CH
2
CH
2
OCOC
8
H
17
)
4-n
, where R is a C
4-8
alkyl group, bis-(&bgr;-methoxycarbonylethyl)-tin-bis-(thio-ethyleneglycol-2-ethylhexoate,-tin-bis-(thioglycolic acid-2-ethylhexoate), -tin dilaurate, -tin dodecyl thiolate and bis-(&bgr;-acetylethyl)-tin-bis-(thioethylene-glycol-2-ethylhexoate), -tin-bis-(thioglycolic-acid-2-ethylhexoate), -tin dilaurate and -tin didodecyl thiolate.
The organotin compounds may be used individually or in admixture with one another in quantities of 0.001 to 0.5% by weight and preferable in quantities of 0.01 to 0.25% by weight, based on the polyol.
By “highly dispersed silica” is meant a silica containing more than 99.8% by weight of SiO
2
which has been produced by hydrolysis of silicon tetrachloride in an oxyhydrogen gas flame. It is commercially available, for example, under the name of “AEROSIL®”.
“Bentonites” are impure clays formed by the weathering of volcanic tuffs. Products available under the name of “BENTONE®” are particularly suitable.
A preferred “thickened aluminosilicate” is absorber paste, more particularly based on castor oil. This is intended to neutralize the effects of moisture in the PUR components. The aluminosilicate concentration is governed by the expected moisture content and is generally between 1 and 12% by weight and more particularly between 2 and 8% by weight, based on the polyol.
The polyol may also contain 0 to 60% by weight and, more particularly, 10 to 30% by weight of at least one filler. It is intended not only to increase the weight and volume, but also to improve useability on a wide scale. Particularly suitable fillers are kaolin, feldspar, mica, silica flour, barium sulfate, aluminium oxides, hydrated aluminium oxides and aluminium hydroxides and also calcium carbonate both as lime spar and as limestone which may be coated. The particle size of the filler is up to 0.05 mm.
Depending on the particular application envisaged, it may be advisable to stabilize the polyurethane against degradation. Suitable antioxidants are, in particular, up to 1.5% by weight of IRGANOX 1010, 1076, 3114 and 1425 antioxidants (products of Ciba Geigy), TOPANOL O antioxidant (a product of ICI) and GOODRITE 3114 antioxidant (a product of Goodrich). Suitable UV absorbers are, in particular, up to 1.5% by weight of TINUVIN P, 328 and 144 UV absorbers (products of Ciba Geigy), SANDUVOR VSU and 3035 UV absorbers (Sandoz), CHIMASSORB 81 UV absorber (a product of Chimosa). Other suitable stabilizers are up to 1.5% by weight of TINUVIN 765 and 770 stabilizer (products of Ciba Geigy), SANDUVOR 3050, 3051 and 3052 (products of Sandoz) and CHIMASSORB 119 stabilizer (a product of Chimosa) and also MARK LA 62, 63, 67 and 68 stabilizers (products of Argus Chemical Corporation).
The binder must be adapted in its composition and quantity to the particle size of the silica sand, more particularly its dust content, and to the application envisaged, more particularly in regard to strength and the water throughflow rate. Thus, any reduction in the particle size increasingly requires special modification of the binder.
The ratio by weight of silica sand to polyurethane binder is preferably less than 20:1 and, more particularly, equal to or less than 16:1. For

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