CA1124929A - Single package additive for thermoplastic formulation - Google Patents

Abstract

SINGLE PACKAGE ADDITIVE FOR THERMOPLASTIC FORMULATION
Abstract of the Disclosure A friable composition single additive package for thermoplastic extrusions is provided in the instant invention. The friable composition can contain paraffin waxes, calcium stearate, various pigments, fillers, lubri-cants, and stabilizers.

Description

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SINGLE PACKAGE ADDITIVE FOR THERMOPLASTIC FORMULATION
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This invention relates to a process for preparing a friable composition from paraffinic hydrocarbon waxes, ; calcium hydroxide and certain fatty acids, or calcium salts of fatty acid, which are solid, glasslike, and remain friable under ambient conditions. These compositions contain a full ~; 5 range of thermoplastic formulation ingredients, including !,' stabilizers. More specifically, this invention relates to compositions which, when placed in discrete particles, have a low tendency to fuse or coalesce compared to paraffinic hydrocarbon waxes and which are capable of being used as a ; 10 single additive for extrusion aids in thermoplastic formula-tions. Such formulations become fluidized under elevated temperatures on the order of 90C or higher.
Thermoplastic extrusion formulations such as those containing polyvinyl chloride, commonly include paraffinic hydrocarbon waxes and calcium salts of some fatty acids, such as calcium stearate, as extrusion aids. These extrusion formulations are generally fed to an extruder as a mixture of particulate solids. It is desirable that any additives ~i to the formulations, including the extrusion aids, be in a ~i 20 discrete, solid particulate form capable of being handled as solids. Unfortunately, the most economically satisfactory materials are also sticky or mushy.
This problem was partially solved in the prior art.
U.S. Patents 3,883,362; 3,883,363; 3,979,345 and 3,986,995 ~, 25 teach a method for producing a friable composition suitable . . .
for use as an extrusion aid in polymeric extrusion formula-tions by mixing a paraffinic hydrocarbon wax with calcium hydroxide and a fatty acid, or a calcium salt of a fatty acid, ~; then heating to a temperature of at least 150C and thereafter;~ 30 cooling to recover a solid, glasslike, friable composition.
These processes were a great advance in the art in that they allowed the use of mushy, low cost, paraffinic waxes instead of the more expensive, high purity waxes. Both types of wax produce excellent results when used in extrusion for-mulations, but low cost paraffinic waxes were difficult to handle. The prior art thus overcame a major objection in ,: , 7 .

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allowing these materials to be handled in a solid, discrete free-flowing 'orm with low tendency to agglomerate.
In these references, it is taught that it is possible to incorporate other additives into the compositions when they are employed as extrusion aids or lubricants. These references state that other processing aids such as poly-ethylene waxes or acrylate polymers may be included. Also pigments such as titanium dioxide, fillers and reinforcing materials can be included.
However, these materials did not include stabilizers, thus preventing the formation of a single package for friable composition additives for thermoplastic extrusions. Stabili-zers, when incorporated using these processes prevented the product from attaining a friable form, leaving them soft, sticky and mushy instead.
It would therefore be of great benefit to provide a method for obtaining a single package of additives in friable, free-flowing form for thermoplastic extrusions.
The package should contain various waxes, pigments, fillers, , 20 reinforcers and stabilizers, the sum of ingredients producing a finished product.
~i It istherefore an object of the instant invention ; to provide a single package, friable composition, free-flowing additives for thermoplastic extrusion. Other object will become apparent to those skilled in this art as the descrip-tion proceeds.
It has now been discovered according to the instant invention that a single package, free-flowing, friable compo-sition for addition to thermoplastic formulations during extrusion can be prepared by a process comprising mixing a , paraffinic hydrocarbon wax with calcium hydroxide and a fatty J acid or a calcium salt of a fatty acid while heating to a temperature of at least 150C, and while at this temperature inserting desired additive materials, including stabilizers which are supported on polyvinyl chloride resins, and there-after cooling to recover a solid, glasslike friable composi-tion, said paraffinic hydrocarbon wax having a drop melting i point or at least 43C and oil content of not greater than 50% by weight and a needle penetration value of 25C in the range of 1 millimeter to 20 millimeters, said fatty acid being a C16 to C24 aliphatic hydrocarbon, monocarboxylic acid or mixtures thereof.
Stabilizers useful in the instant invention are those normally used in stabilizing PVC resin formulations.
Representative examples of such stabilizers are Interstab Chemicals Inc. ET-250 ~rgus Chemical Corp ~RK 1900 ~RX 1925 MARK 1928 *
r~RK 2115 Cincinnati Milacron Chemicals, Inc. TM 181 *

M~T Chemicals, Inc. T 170 Synthetic Products Co. Synpron 1034 ; 15 Cardinal Chemical Co. CC 7710 ~
The stabilizers utilized in the instant invention are effective in forming a single package additive for thermoplastic formulation extrusions. Stabilizers as used :~ in the prior art have not been effective in this application because the product obtained is soft and mushy. Such pro-~ ducts are effective lubricants but cannot be easily stored s and handled in conventional equipment. Such stabilizers can ;;~ be used in the method of the instant invention when first absorbed on PVC resins.
The composition of the instant invention may be prepared by charging the calcium salt of a fatty acid or calcium hydroxide and fatty acid and paraffinic hydrocarbon wax to a heated vessel equipped with an agitator. The wax can be melted before charging to the vessel. Small amounts of water may be present as is known in the grease art.
` ~nder continued agitation, the ingredients are heated to at least 150DC, preferably at least about 160C to about 165C.
During this heatup time, the wax initially becomes molten, forming a continuous phase in which the calcium salt particles ~ ~r ~ ~~

are dis~ersed. After assuming the continuous phase, a su~se~uent increase in viscosity is noticed until the mass reaches a homogeneous, paste-like consistency. As the temperature continues to rise, the paste-like mass breaks into separate phases; a low viscosity oil-like phase and a heavier paste-like phase. The heavier paste-like phase appears to then form soft bead-like masses and the low viscosity oil-like phase disappears into these masses. As the temperature continues to rise, the soft bead-like masses fuse and coalesce into a homogeneous taffy-like material.
It is at this point that the final temperature of about 160C will be reached and the other additives necessary for the package can be added with agitation. Heating may be continued for a short period of time to insure completion of the transformation, even to higher temperatures just short of degradation temperature.
The hot mass, now containing fillers, pigments, : and stabilizer is removed from the vessel and cooled to ambient conditions, whereupon the composition becomes a solid, glass-like friable material which can be ground or otherwise reduced into a particulate form. The particles ; formed will substantially retain their discreteness and ` integrity. The composition is a solid at ambient conditions :~ and can be easily fractured or chopped. However, it is more convenient and somewhat easier to grind the composition under cryogenic conditions. However accomplished, the resultant particulate composition at ambient conditions can be easily handled with conventional solids handling equipment.
The particulate composition, containing all additives necessary for thermoplastic formulation extrusion, will maintain its integrity upon standing or being stored.
It is emphasized at the outset that the composi-tion prepared with the process of this invention is not a mere physical blend wherein each component contributes its individual properties without any interaction with each other. Rather, the physical form of the composition is unlike either of the individual components. The composition is best characterized as being a glass-like, friable solid at ambient conditions, resulting from a synergistic action between the paraffinic wax and calcium salt of a fatty acid or calcium hydroxide and a fatty acid. ~rom a physical chemistry standpoint, it is not known what actually occurs in forming the composition.
Broadly, the process of the invention comprises mixing paraffinic hydrocarbon wax, calcium hydroxide and certain fatty acids while heating the mixture to at least about 150C, preferably at least 160C, adding desired formula material and the specific stabilizer disclosed herein, and thereafter cooling and recovering the solid, glass-like friable composition.
The fatty acids which may be employed are the C16-` C2~ aliphatic hydrocarbon monocarboxylic acids or mixtures thereof. These acids are preferably satùrated. When mixtures of the acids are used, they may contain up to about 15 weight percent of a C14 aliphatic hydrocarbon monocarboxylic acid of the same saturation characteristics outlined above.
~; Illustrative of suitable acids are palmitic, stearic, oleic, , 20 linoleic, eicosanic, behenic, tall oil fatty acid, hydro-~ genated vegetable fatty acid, hydrogenated tallow fatty i~ acid, distilled cottonseed fatty acid, and the like. Various ; commercial grades of suitable acids are available, some of . which are listed in Fatty Acids and Their Industrial .~
Applications by E. S. Patterson, 1968, at Page 7, Table 1-2 ,~ (excluding high lauric). Tnese suitable commercial acids are generally mixtures of the acids hereinbefore described and may additionally have small amounts of certain impurities depending on their method of manufacture.
The calcium hydroxide employed may be any commercial grade material such as slaked lime or hydrated lime.
The suitable paraffinic hydrocarbon waxes are generally derived from petroleum sources. These waxes con-tain a variety of hydrocarbon structures, for example normal paraffins, isoparaffins, cycloparaffins, small quantities of polycyclo-paraffins and aromatics and other hydrocarbons and may be in a purified form or may contain oils depending upon their source and/or manner of recovery. The paraffinic hydrocarbon waxes which are particularly useful are those having a drop melting point (ASTM D 127-63) of at least 110F, preferably at least 145F, an oil content (ASTL>~ D
72165T) of not greater than 50 weight percent, preferably not greater than 20 weight percent, and a needle penetratlon value at 77F (ASTM D 1321-65) in the range of 1 mm to 20 mm, preferably 1 mm to 10 mm.
More specifically, the process of the invention may be carried out by charging the paraffinic hydrocarbon wax, calcium hydroxide and fatty acid to a heated vessel equipped with an agitator. The wax may be premelted before being charged or it may be melted in the vessel. The fatty acid may be handled likewise as appropriate. The calcium hydroxide, being a solid, may be charged using any convenient solids handling means such as an auger.
Representative examples of thermoplastic formula-tions which contain these materials are polyvinylchloride extrusion formulations.
Representative examples of additives currently used in various thermoplastic formulations are set forth. It is emphasized that these additives are by no means exhaustive of those which can be utilized in the instant invention.
However, it is essential to note that the stabilizers in-corporated herein must be first supported on PVC resins in ~ 25 order to obtain a friable product. Additives which can be ; incorporated into the friable compositions include paraffin. wax as an external lubricant, calcium stearate as an internal lubricant, polyethylene as an external lubricant, titanium dioxide as pigments, calcium carbonates as fillers and impact modifiers, and stabilizers of choice.
Representative but non-exhaustive examples of types of methods and examples of which are useful in the instant invention are:
External/Internal Lubricants Paraffin wax Polyethylene wax Oxidized polyethylene wax High molecular weight esters Metal salts (Calcium stearate) 9~:9 ;rncnts Titanium Dioxide Carbon Black Fillers Calcium Carbonate Gypsum (Calcium sulfate) . Talc Silica . Processing Aids i' _ Methacrylate polymers ; Styrene copolymers R -OC -CH2C~2 S(CH2)XCOR

RloccH2cH2 / 5 (CK2 ) CoR2 R OCcH2cH2-sn ~ S(CH2) COR2 `~ S (CH2 ) XCOR2 R~
M - S(CH2)XeOR2 C

: ~1 and M[S(CR2)x 0~ ~3 Rl _ M - S(CH2)XcOR

M = Sn, Sb R = alkyl groups - Cl-C12 R = as before X = as before ~124929 The instant invention is more concretely described with reference to the examples below wherein all parts and percentages are by weight unless otherwise specified. The examples are provided to illustrate the instant invention and not to limit it.
In all experiments set forth below, wax having the physical characteristics described was melted and lime was slurried. The reaction was held at 80 to 90C. Stearic acid was added and the reaction process was agitated for 30 minutes. Heat was increased until the reaction mixture began to build up on the stir blade at about 160 to 165C.
Other ingredients were then added as listed. Examples 1 through 5 are comparative examples showing the use of some commercially available stabilizers when not supported on PVC
resins prior to incorporation. Example 1 shows a tin sta-bilizer alone as an additive. Example 2 shows a tin stabi-lizer with a filler. Example 3 shows the use of another tin stabilizer with filler and pigment. Example 4 shows use of ` a tin stabilizer with polyethylene, filler, and pigment.
Example 5 shows the use of antimony stabilizer. Examples 6 and 7 show the stabilizers of the present invention supported on PVC resin to yield a single package, friable additive.
The same paraffinic wax was used in all examples.
Example 1 Using the general procedure described above, the following materials were charged to the reactor.
Paraffin wax240g (Trademark of and (Code 776)sold by Conoco Inc.) Ca(O~)2 24.6g Stearic acid150g Tin Stabilizer100g (Trademark of and (TM 387)sold by Cincinatti-Milacron) The ingredients were added in the order listed.
After the stabilizer was added to the product, the product became pastelike. After cooling, the product assumed the form of a soft, mushy material.

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Example 2 The following ingredients were charged to the reactor.
: Paraffin wax 240g ; Ca~OH)2 25.9g Stearic acid 149g ,~ CaCO3 600g Tin S~abilizer100g (TM 387) ~ After the stabilizer was added, the product became ; 10sticky and remained so even after cooling to ambient condi-, tions.
~ Example 3 "~, The following materials were added in the order ~$ indicated.
Paraffinic wax270g Ca(OH2) 25g Stearic acid 150g Polyethylene30g (AC-629-A, Trademark of and sold by Allied Chemical Co.) Tio2 200g CaCO3 6G0g Tin Stabilizer80g (Mark 1928, Trademark of and sold by Argus Chemical Co.) ~pon addition of the final stabilizer, the product became a sticky glue. Upon cooling the product attained a paste-like, solid consistency. The product was not friable.
Example 4 The following materials were added in the order set forth.
Paraffinic wax135g Ca(OH)2 12.5g Stearic acid 75g Polyethylene (AC-629-A) 15g Tio2 100g aCO3 300g ~in Stabilizer (Mark 1928) 30g 1~2492g Vpon addition of the final stabilizers, the product became sticky and stringy. Mo friable composition could be formed.
Example 5 The fOllowing materials were ad~e~ in the order descrihed.
Paraffinic wax 270g CatOH)2 25g Stearic acid 150g Polyethylene (~C-629-A) 30g TiO2 200g CaCO3 600g Synpron 103480g (Antimony stabiliz~
trademark of and sold by Synthetic Products) ` 15 Immediately upon addition of the stabilizer, the product became a sticky paste. The paste-like consistency remained when cooled. The product was not friable.
Example 6 Paraffinic wax 11~2g1132g Ca(OH)2 113g Stearic acid 679g Polyethylene (AC-629-A) 136g i2 905g CaCO3 4529g Physical blend of1630g (Trademark of and Tin Stabilizersold by Argus (Mark 1925) andChemical Co.) CONOCO 5385 PVC resin, 1:5 weight ratio, respectively

3~ After completion of the reaction the product was cooled to ambient temperature. The product formed a glass-like, friable compound. When ground to discrete particles, the compound remained friable.

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~xample 7 Paraffinic wax 125g Ca(OH)2 12.5g ~ Stearic acid 75g ; Polyethylene (AC-629A)15q ~ 5 TiO 100g '. CaC03 SOOg Physical blend of time stabilizer (Cincinnati-Milac~on TM-692) and CO~OCO 5385 PVC resin 1:5 weight ratio respectively 180g ;~
After completion of the reaction, the product was cooled to ambient temperature. The product formed a glass-like, friable compound. When ground to discrete particles, the compound remained friable.
Upon addition of PVC with adsorbed stabilizer the reaction products become homogeneous, taffy-like mat-erials. Vpon cooling to ambient temperature (or somewhat below for best results) the product was sufficiently hard to ground to discrete particles. The particles remained discrete and friable under ambient con~itions.
Stabilizers are supported on PVC resin simply by blending the stabilizer with an amount of resin sufficient to absorb and/or support the quantity o~ stabilizer used.
Normally the ratio of stabilizer to resin will range from about 1 to 1 to about 1 to 100 respectively, but from about 1 to 4 to about 1 to 7 is preferred.
In the process of the instant invention, the materials must be 'neated to at least 150C in order to form friable compositions. However, temperatures of 160C
are preferred. The process can be carried out when the fatty acid is mixed with a paraffinic hydrocarbon wax prior to adding the calcium hydroxide. However, the calcium hy-droxide is preferably mixed with a paraffinic hydrocarbon wax prior to adding the fatty acid.

; . . 1~Z4929 ~' The mole ratio of calcium hydroxide to fatty acid ranges from about 0.5 to 1 respectively to about 1 to 1 respectively. However, the preferred range of mole ratios is from about 0.55 to 1 to about 0.65 to 1 respectively.
The weight ratio of wax to calcium salt of the ;; fatty acid is normally in the range of fr~m ~hout 0.3 to 1 to about 2.5 to 1 respectively. However, the preLe;-red weight ratio range of wax of fatty acid is from about 0.6 to 1 to about 1.7 to 1 respectively.
~araffinic hydrocarbon wax of the instant invention should have a drop melting point of at least 43C but a drop melting point of about 60C is preferred.
These waxes should have an oil content of not greater than 50 weight percent by weight but an oil content of not greater than 20 percent by weight is preferred. The needle pene-~ tration value at 25C will fall in the range of from 1 millimiter (mm) to 20 millimeters but a needle penetration value from 1 mm to 10 mm is preferred.
Likewise, the calcium salts which may be employed are those derived from C16 to C24 aliphatic hydrocarbon monocarboxylic acid and mixtures thereof. These acids can be saturated or unsaturated. The mixtures of the acids are used that can contain up to about 15 weight per~ent of the C14 aliphatic hydrocarbon monocarboxylic acid of the same saturation characteristics set forth. Illustrative but non-exhaustive of suitable acids are palmitic, stearic, oleic linoleic, eicosanic, behenic, tall oil fatty acid, hydrogen~
ated vegetable fatty acid, hydrogenated tallow fatty acid, distilled cottonseed fatty acid, and the like. Suitable commercial acids are generally mixtures of the acids described and may additionally have small amounts of certain impurities depending upon their methods of manufacture. Therefore, mixtures of fatty acids can easily be employed.
In addition, the process utilizing the mixture of fatty acids can contain up to about 15% by weight of a C14 aliphatic hydrocarbon monocarboxylic acid.
No one stabilizer need be used alone. Mixtures of these stabilizers can also be used to form a frlable composi-tion.

1~24929 While certain embodiments and details have been ;, shown for the purpose of illustrating this invention, it will be apparent to those skilled in this art that various changes and modifications may be made herein without departing ,. 5 from the spirit or scope of the invention.
, We claim:

Claims (13)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:

1. A process for producing an improved friable composition for addition for thermoplastic formulations during extrusion comprising mixing a paraffinic hydrocarbon wax, calcium hydroxide and a fatty acid, or a calcium salt of a fatty acid while heating to a temperature of at least 150°C thereafter adding desirable additives and a stabilizer and thereafter cooling to recover a solid glass like friable composition, said paraffinic hydrocarbon wax having a drop melting point of at least 43°C, an oil content of not greater than 50 percent by weight and a needle penetration value (25°C) in the range of 1 mm to 20 mm, said fatty acid being a C16-C24 aliphatic hydrocarbon monocarboxylic acid or mixtures thereof; said stabilizer physically blended with sufficient thermoplastic resin to support the quantity of stabilizer used, said blend formed prior to addition to the reaction mixture.

2. A process according to claim 1 wherein the mixture is heated to at least 160°C.

3. A process according to claim 1 wherein the fatty acid is mixed with the paraffinic hydrocarbon wax prior to adding the calcium hydroxide, and wherein the ratio of stablize to thermoplastic resin is from about 1 to 4 to about 1 to 7 by weight, respectively.

4. A process according to claim 1 wherein the calcium hydroxide is mixed with the paraffinic hydrocarbon wax prior to adding the fatty acid.

5. A process according to claim 1 wherein the mole ratio of calcium hydroxide to fatty acid is in the range of 0.5/1 to 1/1.

6. A process according to claim 5 wherein the mole ratio is 0.55/1 to 1/1.

7. A process according to claim 5 wherein the weight ratio of wax to calcium salt of a fatty acid is in the range of 0.3/1 to 2.5/1.

8. A process according to claim 6 wherein the weight ratio of wax to calcium salt of a fatty acid is 0.6/1 to 1.7/1.

9. A process according to claim 2 wherein the paraffin hydrocarbon wax has a drop melting point of at least 60°C, an oil content of not greater than 20 weight percent and a needle penetration value at 25°C in the range of 1 mm to 10 mm.

10. A process according to claim 9 wherein the fatty acid is palmitic, stearic, oleic acid, tall oil fatty acid, eicosanic acid, behenic acid, hydrogenated tallow fatty acid, hydrogenated vegetable oil, or mixtures thereof.

11. A process according to claim 1 wherein a mixture of fatty acids is employed.

12. A process according to claim 11 wherein the mixture of fatty acids contains up to 15 weight percent of C14 aliphatic hydrocarbon monocarboxylic acid.

13. A process according to claim 12 wherein mixtures of stabilizers are used.