CA2216921C - Explosives using glycol still bottoms - Google Patents

Abstract

Explosive compositions are disclosed which comprise a nitrate salt oxidizer and glycol still bottoms alone or in combination with water. The still bottoms function as a fuel oil replacement (FOR) in ANFO explosives. Glycol still bottoms can be mixed with thickeners, cross-linkers and other additives to make a bottoms matrix. The bottoms matr ix and a nitrate salt oxidizer combine to make explosive compositions which show an improvement in performance and water-resistance when compared to standard ANFO explosives.

Description

EXPLOSIVES USING GLYCOL STILL BOTTOMS
Background of the Invention Field: The invention is in the field of explosives, especia:Lly those using nitrate salt oxidizers, and specifically amnion=gum nitrate-fuel oil explosives (ANFO).
State of the art: Explosives and blasting agents are an important part of the mining industry. It is estimated that over three billion pounds of explosives are used each year in the mining industry in the United States alone. The most commonly used explosive is a mixture of about 94% ammon:LUm nitrate (AN) and about 6% fuel oil (FO), commonly referred to as ANFO. It is sold in the form of dry, loose particles cal:Led "prills", generally marketed in bags or in bulk.
Explosive power is measured in terms of weight strength .and bulk strength. The term "weight strength", usually expressed in kilocalories per gram, is used to compare explosives which employ nitrate salt oxidizers with ANFO explosives, the standard for the industry. The value of the weight strength for ANFO is frequently assumed to be 1.0 kcal/gm. Bulk strength, a function of the density of the explosive, is used to compare the explosive power of two products on a bulk or volume basis. The higher the volume density, the higher the bulk strength. Its unit of measure is kilocalories per cubic centimeter, abbreviated kcal/cc.
ANFO is relatively inexpensive and widely used, however, its low volume density (about ~0.8 gm/cc) limits the amount of useful energy that can be obtained per charge. Efforts to increase the density and therefore the bulk strength of ANFO
have included methods using finely ground ammonium nitrate as opposed to nitrate prill particles and the use of high density metallic fuel additives such as aluminum or ferrosilicon.
In addition, ANFO is desensitized by water, precluding its use in water-filled boreholes. In efforts to provide a waterproof SUBSTITUTE SHEET (RULE 26) ANFO, many water-in-oil and oil-in-water emulsion products have been described in numerous patents. Attempts have also been made to waterproof ANFO by using thickeners and cross-linkers;
for example, Sheeran, U.S. Patent No. 4,933,029 and Stromquist and Wathen, U.S. Patent No. 4,693,763.

Not only have there been numerous attempts to increase the explosive power and waterproof properties of ANFO explosives, other attempts have been made to provide for easier handling, transporting and loading of the product. These efforts have met with limited success.
There remains a need in the industry for inexpensive,. easily manufactured explosives having equal or increased explosive power when compared to ANFO which are easily and safely transported, stored, and loaded; are water-resistant; and which have negligible impact on the environment.
Summary of the Invention The invention encompasses explosive compositions comprising a mixture of at least one nitrate salt oxidizer and glycol still bottoms used alone or diluted with water. Alternatively, the glycol still bottoms can be mixed with other additives such as thickeners, cross-linkers and pH adjusters to form a matrix composition, herein termed "bottoms matrix". This matrix composition can then be mixed with at least one nitrate salt oxidizer to form an explosive composition.
Glycol still bottoms, abbreviated to "still bottoms" or "bottoms" herein, have been found to be a suitable replacement for the commonly used fuel oils in ANFO explosives. Therefore, still bottoms plus water or. a bottoms matrix are also herein referred to as "FOR" for "fuel oil replacement". The explosives which use a combination of ammonium nitrate (AN) and ' FOR are herein called "FOR-AN" explosives.
Detailed Description of the Preferred Embodiment Glycol still bottoms are the waste-product remaining in SUBSTITUTE SHEET (RULE 26) P \OPERUtt\CA 2216921 spe.da-3111Y03 distillation units during the process for making marketable glycol products. Primary glycol producers extract ethylene glycol, diethylene glycol, triethylene glycol, and other lower glycols from a mixed glycol starting material. The remaining by-product in the distillation unit after extraction of the lower glycols is used by secondary producers to extract additional lower glycols. The material remaining in distillation units after extraction of the additional lower glycols is a still more concentrated form of a waste product termed glycol still bottoms. Still bottoms comprise a mixture of lower and higher glycols, polyglycols, glycol-ethers as well as various derivatives. Typically, the glycol still bottoms comprise glycols with from 2 to 40 carbon atoms with or without ether linkages.
The glycol still bottoms usually comprise water and at least one component selected from a group consisting of diethylene glycol, diethylene glycol butyl ether, triethylene glycol, triethylene glycol ethyl ether, tetra ethylene glycol, tetra ethylene glycol ethyl ether, tetra ethylene glycol butyl ether, penta ethylene glycol, penta ethylene glycol ethyl ether, penta ethylene glycol hexyl ether, penta ethylene glycol butyl ether, hexa ethylene glycol, hexa ethylene glycol butyl ether, hepta ethylene glycol, hepta ethylene glycol ethyl ether, hepta ethylene glycol butyl ether, octa ethylene glycol ethyl ether, octa ethylene glycol butyl ether, and combinations thereof.
The glycol still bottoms have a high pH value and cannot be used as taken directly from distillation units due to the inherent hazards encountered when handling materials of high pH value.
Neutralization of the still bottoms with HCl renders the bottoms non-hazardous and non-flammable.

P:\OPERVCC\CA 2216921 ape.da-71/12/07 The principal use of glycol still bottoms has been in the coal industry for de-icing. The glycol-rich bottoms prevent individual coal lumps from freezing together during inclement weather, thus avoiding handling problems. This use is limited, however, and at times the disposal of still bottoms has become problematic, often forcing producers to pay for removal.
We have discovered the glycol still bottoms may be used in place of fuel oil to make a nitrate salt explosive. For example, the glycol still bottoms may be used as a replacement for the fuel oil normally mixed with ammonium nitrate to produce an ANFO explosive.
Glycol still bottoms as removed from distillation units, even after neutralization, may still be too viscous for efficient use in the present invention. When thinned with water up to about 35~, the advantageous properties of the bottoms in the manufacture of explosive compositions equal or exceed those of diesel fuel or mineral oil. Usually, additional water comprises between about 8$
and about 35%, for instance between about 18~ and about 35%, by weight of the glycol still bottoms.
In addition to blending well with water, it has been found that still bottoms blend well with nitrate salt oxidizers. It appears that still bottoms are superior when compared to fuel oil in the penetration of ammonium nitrate grill particles. Substantiation by microscopic examination shows efficient filling of the capillaries and interstices of the grill particle. The observed increased density of FOR-AN explosives compared to ANFO explosives supports a finding of increased penetration of grills by the still bottoms.

P:\OPERVct\CA 2216921 spe.da-71!12/07 Still bottoms have a freeze point far below temperatures encountered in mining and quarrying in the United States and Canada and a flash point far above that of fuel oil or mineral oil. The bottoms can easily be pumped and handled, have no known health hazard, and are not regulated in shipment or storage. Also, unlike fuel oil and mineral oil, there is no measurable evaporation of the still bottoms, even when mixed with up to 35$ water, under normal storage conditions.
A typical analysis of glycol still bottoms if found in Table I. A
typical specification for the bottoms is found in Table II. It is anticipated that each batch of glycol still bottoms will have similar characteristics, although analysis and specification data may vary according to content and concentration of the glycols and glycol-ethers which are present. These variations are dependent upon content of the starting material and the operating conditions of processing. However, these variations do not appear to affect the ability of the bottoms to function as a fuel oil replacement.

WO 96/26911 PCT/US95/02 i'26 Table I
,TYPICAL ANALYSIS OF GLYCOL STILL BOTTOMS
ANALYSIS

DIETHYLENE GLYCOL (DEG) 3.71 DEG BUTYL ETHER 2.41 TRIETHYLENE GLYCOL (TEG) 22.68 TEG ETHYL ETHER 3.43 TETRA ETHYLENE (EG) GLYCOL 26.66 TETRA EG ETHYL ETHER 2.08 TETRA EG BUTYL ETHER 1.62 PENTA EG 13.03 PENTA EG ETHYL ETHER 2.85 PENTA EG HEXYL ETHER 1.08 PENTA EG BUTYL ETHER 6.25 HEXA EG 2.50 HEXA EG BUTYL ETHER 6.5 HEPTA EG BUTYL ETHER 4.34 OCTA EG BUTYL ETHER 0.8 II Typical water analysis equals about 10% after neutralization with HC1 to bring pH values to about 6.5-7.

SUBSTiTL)TE SHEET (RULE 2fi) ' CA 02216921 2004-03-31 P:wretevu~cn xzis~zy aoo-nnzro;

TABLE II
TYPICAL SPECIFICATION OF GLYCO STILL BOTTOMS*
GLYCOLS AND DERIVATIVES <95.0$
NON-EVAPORATIVE SOLIDS AT 165°C <16.0$
INORGANIC ASH 8.5$
WATER <10.0$
VISCOSITY AT 0°F 6400 CPS
VISCOSITY AT 50$ WATER SOLUTION AT 0°F 105 CPS
SPECIFIC GRAVITY 1.16 DENSITY 9.67 lbs/gal upH (AFTER NEUTRALIZATION WITH HCl) 6.5 - 7.5 ~*KMCO, INC., Houston, Texas Water can be added to the still bottoms to adjust viscosity before mixing the bottoms with nitrate salt oxidizers. Water can also be added after the bottoms and oxidizer have been mixed. Further, a matrix can be made of bottoms plus water plus other additives and the matrix can then be mixed with nitrate salt oxidizers. In some cases, water can be a solute for nitrate salt oxidizers to become a part of a bottoms matrix. , Commonly used nitrate salt oxidizers of the invention are ammonium nitrate, sodium nitrate, calcium nitrate, magnesium nitrate, and combinations of these. Generally, the nitrate salt oxidizer comprises between about 50 and about 96$ by weight, for example between about 80 to about 95$ by weight, of the explosive composition. Ammonium nitrate is the preferred oxidizer and may be present in the explosive in amounts from about 50$ to 980, more preferably from about 85$ to 96$, by explosive weight. Up to about 50$ of the ammonium nitrate can be replaced with other nitrate salt oxidizers.

P:\OPERUccICA 2216921 spe.doc~211121D3 To render the explosives of the invention a water-resistant, thickener, optionally a cross-linking thickener, is added to the still bottoms to form a bottoms matrix. Rather than a cross-linking thickener, a thickener and a cross-linking agent can be separately added to the bottoms to accomplish the same purpose.
Commonly used thickeners of the invention are cold water swellable and able to produce high viscosities within a matter of hours, for example, guar gums, gum arabic, starches, xanthan gums, polyacrylamide, celluloses, cellulose derivatives, and combinations thereof. Guar gums are presently preferred.
Commercially available cross-linking or non-cross-linking guar gums may be used in the amount of from about 0.2~ to 1.50, more preferably, from about 0.2o to 0.8~. For example, No. 2379 guar gum sold by Rhone-Poulenc, Louisville, Kentucky, contains the cross-linker potassium pyroantimonate. Alternatively, a non-cross-linking guar gum may be used and cross-linking can be accomplished with the addition to the bottoms matrix of about 1.0-1.5$ based on guar gum concentration. Preferably cross-linkers include antimonates, especially potassium antimony tartrate; dichromates;
borates, especially sodium tetratobrate; tannic acids; and other selected organic acids, among other. The antimonates, especially the pyroantimonates are most preferred. Typically, the cross-linking compound is selected from a group consisting of borates, dichromates, antimonates, and combinations thereof.
Other additives to the still bottoms to create a bottoms matrix may include weak acids for pH adjustment. For example, when using gum thickeners with or without cross-linkers, adjustment of the matrix mixture with glacial acetic acid to a final pH of 5.5-6.5 provides for successful completion of chemical reactions.

P'\OPERVcc\CA 2216921 ape.dx-7U12/03 T.he following examples compare FOR-AN explosives of the invention to the standard results obtained with ANFO explosives.
Characteristics of ANFO explosives are commonly known in the industry. The examples demonstrate performance of the invention under both unconfiNed above-ground conditions and dry mine field conditions.

Example 1 The first propagated above-ground unconfined test shootings of the FOR-AN explosives of the invention employed a formulation compounded from glycol still bottoms and ammonium nitrate grills.
a The mixture for explosive Charge 1 of this example was hand-mixed using conventional bench-top techniques. Glycol still bottoms purchased from KMCO, Inc. , containing about 10%-12% H20 at pH 6.5-7.5, were mixed with additional water to give the still bottoms a 19~ water content. The bottoms were then mixed with ammonium nitrate grills in the proportions given in Table III.
One Thousand grams of the charge mixtures as described above were packed into cardboard cylinders, measuring 3 and 4 inches in diameter and 10 inches in length to give a density of 1 gm/cc. One hundred twenty grams of pentolite equivalent primer was packed into the top end of the cylinders. The results of this example were that all charges detonated, showing similar sensitivity and bulk strength as commonly expected using ANFO
explosives.
In this Example and in Examples 2 through 4 describing the unconfined tests, the term "detonation" means that the main charge, when primed and initiated, tripped or detonated a 25 grain detonating cord embedded in the charge at the cylinder end opposite the primer initiation end. In the field tests, "detonation" was measured as a visually estimated disturbance or fragmentation in the earth or rock surrounding the charges.
In underwater tests, "detonation" was measured with instruments.
The ammonium nitrate grills in this and the following examples were obtained from either LaRoche Chemicals, Geneva, Utah or ,.
Wycon Chemicals, Cheyenne, Wyoming. Other sources of ammonium nitrate grills which have been successfully used with glycol SUBSTITUTE SHEET (RULE 26) WO 96!26911 PCT/US95l02'726 still battoms to make the explosive compositions of the invention have been supplied by ICI Chemical Company, Calgary, Alberta, Canada; IRECO, Donora, Pennsylvania; ETI Chemicals, Seneca, Illinois; and Nitrochem, Ontario, Canada.
As indicated above, the glycol bottoms used in the Examples i were obtained from KMCO, Inc., Houston, Texas.
Table III
EXPLOSIVE CHARGE FORMULATIONS
CHARGE 1 Mixture (% explosive weight) Still Bottoms (19% H20) 13%
Ammonium Nitrate Prills 87%
CHARGE 2 Mixture (% explosive weight) Bottoms Matrix 15%
Ammonium Nitrate 85%
Bottoms Matrix (% matrix weight) Still Bottoms (19% HZO) 65%
Ammonium Nitrate Prills 30%
Hz0 5 Example 2 Materials and methods were essentially the same as described. in Example 1. The formulation of the explosives consisted of 8%
still bottoms (19% H20) and 92% of ammonium nitrate prills.
One thousand grams of the explosive was packed into cardboard ' cylinders measuring 3 inches, 3.5 inches and 4 inches in diameter and 12 inches in length. One hundred twenty grams of pentolite equivalent primer was used. All charges detonated showing similar sensitivity and bulk strength as commonly exhibited by ANFO explosives.

SUBSTtTLJTE SHEET (RULE 26) Example 3 Other repetitive unconfined tests were performed using mixtures of still bottoms and ammonium nitrate prills in which the water content of the still bottoms was varied to account for up to 35~ of the bottoms (up to about 3.5% of the explosive).
Materials and methods for making the charges were essentially the same as in Charge 1 of Example 1. Formulations for high-water content charges are found in Table IV. These tests showed results similar to the results from the Examples 1 and 2 test detonations. Detonations occurred in each case.
The unexpected results of the tests of this Example are that the FOR-AN explosives did detonate. ANFO explosives containing this amount of water would not be predicted to detonate. Water present in the FOR-AN explosive charges in amounts of 2.4o to 3.5% gave no evidence of deterrence of energy production. In contrast, it is commonly known that water acts as an energy deterrent when present in ANFO explosives in amounts over 1.0~
to 1.5~.
Table IV
EXPLOSIVE CHARGE FORMULATIONS
Charge 1 Mixture Still Bottoms (30o Hz0) Ammonium Nitrate Prills 92%
Charge 2 Mixture Still Bottoms (35% H20) 80 Ammonium Nitrate Prills 92%
Example 4 Further repetitive unconfined tests were completed using the explosive charges of the formulations illustrated in Table V.
SUBSTITUTE SHEET (RULE 26) W O 96J26911 PCTlUS95102726 To make the bottoms matrix for Charges 1 and 2, a small amount of still bottoms (10% H20) was mixed with water and then w~~th the gum. The remainder of the still bottoms and 'water wEare added to the mixture.
To make the bottoms matrix for Charge 3, a mixture of water <~nd d calcium nitrate was added to the still bottoms. Then a small amount of-this mixture was added to the gum. After the gum was absorbed, the remainder of the still bottoms, water, and calcium nitrate mixture was added.
The resulting bottoms matrix mixtures in each case were adjusted to a pH of 5.5 with glacial acetic acid and then added to the ammonium nitrate prills in the proportions given in Table V.
The charge mixtures not only exhibited a viscous consistency and appearance, water resistance was apparent, especially in charge mixture 2. The No. 2379 gum contained a cross-linker, potassium pyroantimonate, which assisted in forming a more viscous bottoms matrix.
The charge mixtures weighing about 762 grams each were loaded into cylinders measuring three to five inches in diameter and ten inches in length. One hundred twenty-five grams of pentolite equivalent primer was used to detonate the charges.
Visually superior results were obtained using the FOF:-AN
explosives as compared to commonly known results using p,NFO
explosives.

SUBSTITUTE SHEET {RULE 2fi) TABLE V
EXPLOSIVE CHARGE FORMULATIONS
Charge 1 Mixture (% explosive weight) Bottoms Matrix 15.0% <

Ammonium Nitrate Prills 85.0%

Bottoms Matrix (% matrix weight) HZO - 3 4 . 0 %

No. 8000 guar gum* 0.5%

Glacial acetic acid 0.5%

Still Bottoms (19% H20) 65.0%

Density = 1.01 gm/cc *Rhone-Poulenc, Louisville, Kentucky Charge 2 Mixture (% explosive weight) Bottoms Matrix 17.0%

Ammonium Nitrate Prills 83.0%

Bottoms Matrix (% matrix weight) -Calcium nitrate 30.0%

Hz0 31 . 0 No. 2379 guar gum** 0.6%

Glacial acetic acid 0.4%

Still Bottoms ( 19 % H20) 38 . 0%

Density = 1.13 gm/cc **Contains cross-linking agent, potassium pyroantimonate Charge 3 Mixture (% explosive weight) Bottoms Matrix 15.0%

Ammonium Nitrate Prills 85.0%

Bottoms Matrix (% matrix weight) H20 32.0%

Calcium nitrate 20.0%

No. 8000 guar gum 0.5%

Glacial acetic acid 0.5%

Still Bottoms (19% Hz0) 47.0% ' Density = 1.10 gm/cc SUBSTITUTE SHEET (RULE 26~

WO 96126911 PCT/US95/02'726 Example 5 A field test was conducted in a West Virginia coal mine. Using a backhoe, charge material was mixed in the bucket and loaded into nine inch diameter bore holes which were nineteen to r twenty feet deep and arranged in a twenty-five foot by twenty-five foot pattern. The charge material consisted of 8% still bottoms (19% H20) and 92% ammonium nitrate prills. FOR.-AN
explosives were compared to Heavy ANFO explosives (HANFO), which are explosives made from an emulsion of oil-in-water plus ammonium nitrate. FOR-AN charges contained 20% less weight: of explosive in each hole than did the HANFO charge, i.e., typically 320 lbs. of charge material were placed into the HANFO holes compared to 260 lbs. in the FOR-AN holes. The density of the FOR-AN explosive was 0.95-0.97 g./cc. The density of the HANFO explosive was about 1.2 gm/cc. All charges detonated. After shooting, fragmentation was visually compared. No~apparent differences were observed between the results of the FOR-AN detonations and the results of the HANFO
detonations.
Example 6 Field tests were preformed in Pennsylvania in order to compare the explosive strength of FOR-AN explosives to ANFO explosives.
ANFO and FOR-AN explosives were prepared using the methods of Example 5. ANFO explosive mixtures consisting of 6% minEaral oil and 94% ammonium nitrate prills were packed to give a density of 0.83 gm/cc. FOR-AN explosive mixtures of the formulation in Table VI were packed to give a density of 0.96 gm/cc. Holes were dug to be about 6 inches in diameter and 43 feet deep, arranged in a pattern of a 16 foot spacing by a 16 foot burden. Approximately one-half of the holes were fi:Lled with about 330 lbs. each of ANFO explosives and the other half with 311 lbs. each of FOR-AN explosives.
After shooting, damage fragmentation was visually compared. No apparent differences were observed between the results of the FOR-AN detonations and the results of the ANFO detonations.

SUBSTITUTE SHEET (RULE 26) Table VI
EXPLOSIVES CHARGE FORMULATION
Charge Mixture (% explosive weight) Bottoms Matrix 15.0%
Ammonium Nitrate Prills 85.0%
Bottoms Matrix (% matrix weight) H20 35.0%
No. 8000 guar gum 0.4%
No. 2379 guar gum 0.4%
Glacial acetic acid 0.2%
Still Bottoms (25% H20) 64.0%
Density averaged 1.05 to 1.08 gm/cc.
The observations and conclusions drawn from Examples 1 through 6 indicate the following:
1. The FOR-AN explosive compositions of this invention show an increase in density when compared to ANFO explosive compositions. It follows that a corresponding increase in weight and bulk strength will be observed for FOR-AN explosives when compared to ANFO explosives of the same weight.
2. Increased water-resistance is demonstrated for FOR-AN
explosives when compared to standard ANFO explosives.
3. Penetration of individual prill particles of AN by the glycol still bottoms in FOR-AN explosives is superior to fuel oil or mineral oil penetration of AN in ANFO explosives.
This is suggested to be a major factor in benefits in performance demonstrated in comparative tests.
The invention has been described using glycol still bottoms as a waste product in distillation units after extraction of lower SUBSTITUTE SHEET (RULE 26) WO 96/26911 PCT/US95/02i'26 glycols from a mixed glycol starting material. The use of sv.ch waste material is presently preferred because of its status as a waste material, its availability and resulting low cost. It should be realized that the still bottoms as defined herein could be specifically manufactured for use in the invention rather than merely collected as a waste product. When specifically manufactured, the still bottoms mixture c:an include, in addition to water up to about 350, any one or more of.the glycols listed in Table 1.
Whereas this invention is here illustrated and described w:Lth reference to embodiments thereof presently contemplated as i~he best mode of carrying out such invention in actual practice, it is to be understood that various changes may be made in adapting the invention to different embodiments without departing from the broader inventive concepts disclosed herein and comprehended by the claims that follow.

SUBSTITUTE SHEET (RULE 26)

Claims (17)

Claims

1. An explosive composition comprising at least one nitrate salt oxidizer and glycol still bottoms.

2. An explosive composition comprising at least one nitrate salt oxidizer, glycol still bottoms, and additional water.

3. A bottoms matrix composition to be added to at least one nitrate salt oxidizer to produce an explosive composition, comprising glycol still bottoms, additional water, and a thickener.

4. An explosive composition comprising at least one nitrate salt oxidizer and a bottoms matrix composition which includes glycol still bottoms.

5. A composition according to Claim 1, 2, 3, or 4, wherein the glycol still bottoms comprise glycols with from 2 to 40 carbon atoms with and without ether linkages.

6. A composition according to Claim 1, 2, 3, or 4, wherein the glycol still bottoms comprise water and at least one component selected from a group consisting of diethylene glycol, diethylene glycol butyl ether, triethylene glycol, triethylene glycol ethyl ether, tetra ethylene glycol, tetra ethylene glycol ethyl ether, tetra ethylene glycol butyl ether, penta ethylene glycol, penta ethylene glycol ethyl ether, penta ethylene glycol hexyl ether, penta ethylene glycol butyl ether, hexa ethylene glycol, hexa ethylene glycol butyl ether, hepta ethylene glycol, hepta ethylene glycol ethyl ether, hepta ethylene glycol butyl ether, octa ethylene glycol ethyl ether, octa ethylene glycol butyl ether, and combinations thereof.

7. ~An explosive composition according to Claim 1, 2, or 4, wherein the nitrate salt oxidizer is selected from the group consisting of ammonium nitrate, calcium nitrate, sodium nitrate, magnesium nitrate, and combinations thereof.

8. ~An explosive composition according to Claim 1, 2, or 4, wherein the nitrate salt oxidizer comprises between about 50% and about 96% by weight of the explosive composition.

9. ~An explosive composition according to Claim 1, 2 or 4, wherein the nitrate salt oxidizer comprises between about 80% and about 95% by weight of the composition.

10. A composition according to Claim 2 or 3, wherein the additional water comprises between about 8% and about 35% by weight of the glycol still bottoms.

11. A composition according to Claim 2 or 3, wherein the additional water comprises between about 18% and about 35% by weight of the glycol still bottoms.

12. A composition according to Claim 3, wherein the thickener is selected from the group consisting of guar gums, gums arabic, starches, xanthan gums, polyacrylamides, celluloses, cellulose derivatives, and combinations thereof.

13. A composition according to Claim 3, wherein the thickener comprises a guar gum.

14, A composition according to claim 13, wherein the guar gum contains a cross-linking compound.

15. A composition according to Claim 3, further comprising a cross-linking compound.

16. A composition according to Claim 14 or 15, wherein the cross-linking compound is selected from the group consisting of borates, dichromates, antimonates, and combinations thereof.

17. A composition according to Claim 3, further comprising a pH
adjuster.