CA1246822A - Process for pre-treating castable polyester resin - Google Patents
Process for pre-treating castable polyester resinInfo
- Publication number
- CA1246822A CA1246822A CA000453791A CA453791A CA1246822A CA 1246822 A CA1246822 A CA 1246822A CA 000453791 A CA000453791 A CA 000453791A CA 453791 A CA453791 A CA 453791A CA 1246822 A CA1246822 A CA 1246822A
- Authority
- CA
- Canada
- Prior art keywords
- blend
- polyester resin
- vibrating
- mold
- process according
- 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
Links
- 238000000034 method Methods 0.000 title claims abstract description 37
- 230000008569 process Effects 0.000 title claims abstract description 31
- 229920001225 polyester resin Polymers 0.000 title claims description 14
- 239000004645 polyester resin Substances 0.000 title claims description 14
- 239000000203 mixture Substances 0.000 claims abstract description 60
- 238000010008 shearing Methods 0.000 claims abstract description 21
- 239000004579 marble Substances 0.000 claims abstract description 18
- 239000011159 matrix material Substances 0.000 claims abstract description 13
- 239000007788 liquid Substances 0.000 claims abstract description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 17
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 12
- 239000000945 filler Substances 0.000 claims description 12
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 10
- 239000003054 catalyst Substances 0.000 claims description 7
- 229920006337 unsaturated polyester resin Polymers 0.000 claims description 7
- RREGISFBPQOLTM-UHFFFAOYSA-N alumane;trihydrate Chemical compound O.O.O.[AlH3] RREGISFBPQOLTM-UHFFFAOYSA-N 0.000 claims description 5
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 5
- JPSKCQCQZUGWNM-UHFFFAOYSA-N 2,7-Oxepanedione Chemical compound O=C1CCCCC(=O)O1 JPSKCQCQZUGWNM-UHFFFAOYSA-N 0.000 claims description 4
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 claims description 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 4
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 4
- 229910052753 mercury Inorganic materials 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 229920005989 resin Polymers 0.000 claims description 4
- 239000011347 resin Substances 0.000 claims description 4
- 239000003039 volatile agent Substances 0.000 claims description 4
- 238000010923 batch production Methods 0.000 claims description 3
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 3
- 238000009472 formulation Methods 0.000 claims description 3
- 239000000049 pigment Substances 0.000 claims description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 3
- 229920001187 thermosetting polymer Polymers 0.000 claims description 3
- 239000011521 glass Substances 0.000 claims description 2
- 238000004132 cross linking Methods 0.000 claims 5
- 239000000178 monomer Substances 0.000 claims 5
- 239000013530 defoamer Substances 0.000 claims 2
- 239000002518 antifoaming agent Substances 0.000 claims 1
- 238000010924 continuous production Methods 0.000 claims 1
- 238000000465 moulding Methods 0.000 claims 1
- 238000005266 casting Methods 0.000 abstract description 9
- 229920000728 polyester Polymers 0.000 abstract description 2
- 239000000463 material Substances 0.000 description 7
- 230000009471 action Effects 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 238000007872 degassing Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229940094070 ambien Drugs 0.000 description 1
- 239000002928 artificial marble Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 230000005226 mechanical processes and functions Effects 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- ZAFYATHCZYHLPB-UHFFFAOYSA-N zolpidem Chemical compound N1=C2C=CC(C)=CN2C(CC(=O)N(C)C)=C1C1=CC=C(C)C=C1 ZAFYATHCZYHLPB-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
A pretreatment process to remove entrapped air from liquid polyester blends intended as the matrix of cast marble is disclosed. The formulated blend is subjected to a simultaneous evacuating, vibrating and shearing step which is critical within broad parameters. The thus treated blend, after casting, will be non-porous in cross section, thereby making it suitable for countertops and other parts which must be field cut to specifications.
A pretreatment process to remove entrapped air from liquid polyester blends intended as the matrix of cast marble is disclosed. The formulated blend is subjected to a simultaneous evacuating, vibrating and shearing step which is critical within broad parameters. The thus treated blend, after casting, will be non-porous in cross section, thereby making it suitable for countertops and other parts which must be field cut to specifications.
Description
~24682Z
PROC~', FOR PR~-TREATING C~Tl~i3L~ POLY~T~R RL~IN
BAC~GROUND 3F ~,~ VtNI:~
Field of the Invention ______ This invention relates to synthe~ic reslns, and more particularly to processes for casting polyester resin.
tio_ of the Prior Art Cast unsaturated polyesters using inert fillers is an art which has been prac~tlced commerclally since the early 1960's.
Products are known variously as cultured marble, cast marble, precast marble and molded marble. In the 1370's, a synthetlc onyx was developed using dlfferent fillers. Products in both marble and onyx include table tops, lamp bases, window sills, countertops, wall panels and various items of sanitary-ware such as vanity tops, bathtubs and showers.
Typically, cast marble consists of 20-35~ unsaturated polyester resin such as, for example, propylene glycol esterified with adipic and maleic anhydride and filled with an inert material such as calcium carbonate. Cast onyx consists of a specially clarified polyester resin with glass frlt and aluminum trihydrate used either separately or in combination as the filler. The conventional manufacturing process consists of the ~ollowing steps:
(1) preparing tne molds by covering the surface with a suitable mold release agent, typically a wax or organic alcohol.
PROC~', FOR PR~-TREATING C~Tl~i3L~ POLY~T~R RL~IN
BAC~GROUND 3F ~,~ VtNI:~
Field of the Invention ______ This invention relates to synthe~ic reslns, and more particularly to processes for casting polyester resin.
tio_ of the Prior Art Cast unsaturated polyesters using inert fillers is an art which has been prac~tlced commerclally since the early 1960's.
Products are known variously as cultured marble, cast marble, precast marble and molded marble. In the 1370's, a synthetlc onyx was developed using dlfferent fillers. Products in both marble and onyx include table tops, lamp bases, window sills, countertops, wall panels and various items of sanitary-ware such as vanity tops, bathtubs and showers.
Typically, cast marble consists of 20-35~ unsaturated polyester resin such as, for example, propylene glycol esterified with adipic and maleic anhydride and filled with an inert material such as calcium carbonate. Cast onyx consists of a specially clarified polyester resin with glass frlt and aluminum trihydrate used either separately or in combination as the filler. The conventional manufacturing process consists of the ~ollowing steps:
(1) preparing tne molds by covering the surface with a suitable mold release agent, typically a wax or organic alcohol.
(2) sprayin~ the mold surface with a clear, unsaturated polyester resin referred to as a gel coat into which has been incorporated an ultravlolet stabili~er and a thixatrope. An ~.
~246t3~Z
orgallic peroxide i5 used as catalyst.
~246t3~Z
orgallic peroxide i5 used as catalyst.
(3) after the gel coat nas partially cured, a matrix is troweled or poured into the m~ld. The matrix is prepared by mixing polyester resin, organic peroxide catalyst, filler and olorants in the desired proportions.
(4) after the molds are filled, they are vibrated for several minutes to try to effec~t air release from the matrix, but especially From the interface with the gel coat.
(5) the material is then allowed to cure at ambien~
temperature to a hard and "rigid" state before removal of the formed part from the mold.
A typical example -- U.S. 3,562,379 to Duggins --discloses an improved cast marble polyester resin process. U.S.
3,562,379 and U.S. 3,488,346 are also examples of the advanced state of the art.
Cast marble has only one real competitor~ In the 1960's, du Pont developed an aluminum trihydrate filled methylm thacrylate polymer which it has marketed under the mark "Corian". In competing with methylmethacrylate polymer, cast marble has had several significant advantages. It can be manufacturea at a lower cost, it has considerably greater versatility as to colors, shapes and sizes, and its physical properties are better. In addition, it is more satisfac~torily repairable.
The major disadvantage of cast marble has been its lac~k o machineability because of the porosity of the matrix resulting from lncomplete rernoval of entrapped air during the casting operation. Vibrating, as practiced conventionally, is inadequate to remove the air, This has effectively ruled out cast marble in the kitchen countertop market where traditionally `Ir~ 2-~2~822 the count*rtops are fiel~ cut tO speciFlc requirements.
De-gassinq agents such as disclosed in U.~ 4,129,543 ~o Kaplan have been used, but witn limited success due to the hlqh viscosity of the resin which inhibits air release. Further, they are expensive in the large quantities called for in, for example, the Kaplan patent and which quantities have heretofore been necessary to achieve even limited success and which, accordlng to the Kaplan patent, may result in surface charring Evacuating the blend in the mold tends to devolve styrene monomer preferential ~o deyassing the air and, further, it is not economically feasible to put the large molds common to the industry in vacuum chambers.
There is, therefore, a need for a simple, economical cast marble process which will remove entrapped air from a polyester resin to leave a uniformly dense matrix and to accomplish this end result without deliterious efects on the polymerization process itself~
SU~MARY OF THE INVENTION
The aforementioned prior art problems are solved by the process of this invention in which castable polyester resin is mechanically pre-treated before the casting process in a critical combination of process steps to rupture and release entrapped air, leaving thereby a material which, atter hardening, may be machined and the exposed edges will be nonporous and uniform, giving a pleasing appearance.
In the process of this invention, an unsaturated polyester resin such as, for example, propylene glycol esterified with adipic and maleic anhydride of about 600 to about 3000 centipoise viscosity, and containing styrene monomer ~24~822 as a crc~ss linking agent is first formulated by adding an organi~ peroxide and solid filler material such as calcium carbonate in the conventional manner to form a blend of about 20 to about ~0 weight perçent of polyester resln and about 60 to abo~t ~0 weight petcent iller~ In a batch process, this simply means mixing these materlals together.
The blend is then transferred to a vacuum vessel. This vessel must include means to allow the blend to be subjected to a shearing action such as, for example, by rocking action or mechanical agitation such as using a slow speed stirrer, and to simultaneously subject the blend to vibration, all while a vacuum is being applied. These three process steps --evacuating, vibrating and shearing -- are req~ired to be done concurrently and are criti-al within certain broad parameters.
For example, the vacuum should be between about 15 to about 3Q
inches of mercury and the vibration is preferable at about 2,000 to about 4,000 cycles per minute.
The mechanisms of this process are (1) to invoke migration of entrapped air to the surface by means of applying a vacuum and vibration, and (2~ to facilltate release of this air upon its reaching the surface by shearing of the bubbles by some mechanical means~ The latter mechanism is assisted by incorporating into the blend an anti-~oam or air release agent whose function is to reduce the surface tension of the liquid.
The shearing action is accomplished preferably by rocking the vessel gently over a total of about a 60 degree arc as measured rom a line perpendicular to the horizontal plane of the blend.
A preferred embodlment also includes performing the shearing step by inserting into the blend a baffle comprising a series of fingers between which the blend passes as it is being rocked.
~2~6~22 rhe just-described eva(uatirlg, vlbrating and shearing are critical as to co~bination. That is, all are required simultaneously. !10wever, there ls permissible variation as to the time and quantum. These steps will effectively remove entrapped air which heretofore has been ineffectively removed by other process steps or by the use of degassing or defoaming chemical agents.
After thls pretreatment step, it is generally necessary to vibrate the blend agaln. This vibrating step is accomplished without any accompanying evacuation or shearing and is merely for the purpose of re-incorporating devolved volatiles such as styrene monomer, the entrapped alr now being no longer present.
This last process step can be accomplished after the blend has been poured into a mold, in which case the vibrator is merely attached to the mold's exterior surface.
The afore~entioned pretreating process produces a blend which may be utilized in all conventional casting processes and will produce a cured rigid material, or part, which is substantially void free in cross section. This means that cast marble, which has heretofore been limited to uses as bathroom sinks, table tops, lamps, etc. which are totally precast and merely installed in the Field, can now be expanded to such applications as countertops for kitchens, bars, etc. wher~ the material to be used must be cu. to fit on the job site.
The cast marble produced by the pretreating process of this invention is pleasing to the eye in cross section and inherently stronger due to the absence of voids in the material.
BRIEF DESCRIPTION OF THE DRA~ING(S) Figure l is a flow diagram showing the process steps of this lnvention~
Figure 2 illustrates as a s~hematic~ drawing, a preferred embodiment of the concur~ently performed shearing, vibrating and evacuating step.
Figure 3, a front vlew taken along lines 3--3 of Eigure 2, shows, in longitudinal cross section, an evacua~ing vessel containing a baffle suitable for use in the process of this invention.
DETAILED DESCRIPTION OF TH~ PREFERRED EMBODIMENT(S) Referring now to the drawings, and more particularly to Figure 1 and at arrow 10, the words "to mlxer" are intended to indicate the formulation of a liquid thermosetting polyester resin in a typical batch mlxture as lndicated in Example I
below:
Exam~le I
,'J 300 grams of polyester resin; 1,200 cp; Silman 585 brand ,,r; ~
700 grams of calclum carbonate filler; 325 mesh Pfizer FGD brand grams of 50 percent methyl ethyl ketone peroxide;
Superox 709 Reichold Chemicals brand are mlxed together. Up to 200 parts per mlllion of poly dimethyl siloxane, Union Carbide SAG 100 may be added, if desired~ Any larger amount is not required and the siloxane may be eliminated altogether. The resulting mixture is blend-ed as indi~ated at step 12 for about five minutes or as long as needed to thoroughly blend the mix. The mix is then transferred as indicated by arrow 14 to a vacuum vessel as indicated at block 16. The vacuum vessel is preferably a rocking vessel capable of til~lng at least 30 degrees from vertical in each direction for ~ lr~ k ~Z~6822 a total arc o~ rotation of 60 degrees. The vessel includes means to induce rocking at a frequenc~y oF one to two cycles per minute during the evacuation cycle. Addltionally, a vibrator is attached to the vessel to induce a vibration cycle of From about 2,00~ to about 4,000 cycles per minute.
The combined steps o~ evacuatlon, vibration and shearing are performed for about thirty minutes which for a mix of this volum~ has been found su FFicient to rupture and rel~ase substantially all the entrapped air.
This shearing action thus des~ribed is facilitated by placing, in the vessel prior to the sealing and evacuation, a baffle consisting of a linear series of fingers which extend into the blend so that the blend must pass between the fingers during the rocking cycle.
Following completion of the thirty minute evacuating, shearing and vibrating step, the vessel is opened, a pigment or colorant such as two ounces of titanium dioxide are added to the blend, as is conventional in this art, and the blend, or matrix, is then transferred as indicated at arrow 18 to a mold.
~ fter the blend is poured or trowled into a mold (which may be prepared with a gel coat, etc. as is well known in the art~, the mold is vibrated, again at about 2,000 to 4,000 cycles per minute, for a period o~ about 15 minutes to facilitate redisolving of styrene monomer. At this step in the process, it is important to note that vibration is not for the purpose of releasing air, in as much as little or no air is left, and the vibration at this point would be ineffective for this purpose anyway, as the prior art makes clear. That is, vibration as indicate~ by step 21 in Figure 1 is for the sole purpose of re-incorporating the devolved volatiles such as styrene monomer ~2~682;~
back into ~he hlend. Devolving styrene can be readily seen by surface bubble formation and the vibrating step may be eliminated if no devolving takes place.
Referring now to Figure 2, the critical combination step of evac~uating, shearing and vlbrating step is shown schematically. In Flgure 2, vessel 20 is shown diagramatically to bett*r illustrate the shearing process. In Figure 2, vessel is shown first at rest as indicated by lead line 22 and showing blend 24 at rest> Also shown in Figure 2 are two additional positions of vessel 20, both illustrated in phantom and each showing a 30 degree arc as indicated by arrow 26.
Thus, the total ar- of rocking of vessel 20 is 60 degrees as lndicated by arrow 28.
Also shown in cross section in Figure 2 is baffle 30 which is better illustrated by reference now to Figure 3, In Figure 3, taken along lines 3--3 of Figure 2, vessel 20 is shown in cross section again but with baffle 30 shown in front elevation, including fingers 32 between which blend 24 passes during the rocking of vessel 20 which gives rise to the shearing step of the process as previously desc~ribed.
Following the completion of the shearing, evacuating and vibrating step, vessel 20 is opened. ~t this point, the colorants or pigments as previously described in Example I are added. Blend 2¢ is now transferred to a previo~sly prepared mold as indicated at arrow 18 in Figure 1, and which has prevlously been describecl including a gel coating applied in the conventional manner.
There are many variations which may be practiced within the scope of this invention. For example, while described and illustrated as a batch process, th* process steps may be ~2~682Z
co~ined Wi.ttl d continlJous coatiny process.
Also, although illustrated as a casting process, since the process of this invention ls dir~cted to pre-casting, the part forming step itself is not limited to casting, but is also suitable for injection ~olding as well as all other part ~orming steps.
Also, this invention ls not llmlted to a rigid mold. A
nonrigid, or flexible, mold such is common for decorative items like lamp bases may be used, or parts may be cast ln flexlble molds using wood fillers such as is common for furniture parts.
It should be noted that clear casting resins without fillers may be used such as is common for decorative items.
There are many advantages to the pre-treatment process of this invention. Chiefly is the ability to manufacture cast marble items or parts which are nonporous and, thus, may be machined or cut to leave an exposed edge which is pleasing to the eye. The use of lnexpensive mechanical process steps eliminates the need for expensive, and largely ineffective, chemical degassing additives.
Improved physical properties including greater tensile strength (resistance to thermal and mechanical stresses) and greater bond strength between the matrix and the gel coat are additional advantages achieved by the use of the process of this invention.
Having now illustrated and described my invention, it is not intended that such description limit this invention, but rather that this invention be limited only a reasonable interpretation of the apended Claims.
temperature to a hard and "rigid" state before removal of the formed part from the mold.
A typical example -- U.S. 3,562,379 to Duggins --discloses an improved cast marble polyester resin process. U.S.
3,562,379 and U.S. 3,488,346 are also examples of the advanced state of the art.
Cast marble has only one real competitor~ In the 1960's, du Pont developed an aluminum trihydrate filled methylm thacrylate polymer which it has marketed under the mark "Corian". In competing with methylmethacrylate polymer, cast marble has had several significant advantages. It can be manufacturea at a lower cost, it has considerably greater versatility as to colors, shapes and sizes, and its physical properties are better. In addition, it is more satisfac~torily repairable.
The major disadvantage of cast marble has been its lac~k o machineability because of the porosity of the matrix resulting from lncomplete rernoval of entrapped air during the casting operation. Vibrating, as practiced conventionally, is inadequate to remove the air, This has effectively ruled out cast marble in the kitchen countertop market where traditionally `Ir~ 2-~2~822 the count*rtops are fiel~ cut tO speciFlc requirements.
De-gassinq agents such as disclosed in U.~ 4,129,543 ~o Kaplan have been used, but witn limited success due to the hlqh viscosity of the resin which inhibits air release. Further, they are expensive in the large quantities called for in, for example, the Kaplan patent and which quantities have heretofore been necessary to achieve even limited success and which, accordlng to the Kaplan patent, may result in surface charring Evacuating the blend in the mold tends to devolve styrene monomer preferential ~o deyassing the air and, further, it is not economically feasible to put the large molds common to the industry in vacuum chambers.
There is, therefore, a need for a simple, economical cast marble process which will remove entrapped air from a polyester resin to leave a uniformly dense matrix and to accomplish this end result without deliterious efects on the polymerization process itself~
SU~MARY OF THE INVENTION
The aforementioned prior art problems are solved by the process of this invention in which castable polyester resin is mechanically pre-treated before the casting process in a critical combination of process steps to rupture and release entrapped air, leaving thereby a material which, atter hardening, may be machined and the exposed edges will be nonporous and uniform, giving a pleasing appearance.
In the process of this invention, an unsaturated polyester resin such as, for example, propylene glycol esterified with adipic and maleic anhydride of about 600 to about 3000 centipoise viscosity, and containing styrene monomer ~24~822 as a crc~ss linking agent is first formulated by adding an organi~ peroxide and solid filler material such as calcium carbonate in the conventional manner to form a blend of about 20 to about ~0 weight perçent of polyester resln and about 60 to abo~t ~0 weight petcent iller~ In a batch process, this simply means mixing these materlals together.
The blend is then transferred to a vacuum vessel. This vessel must include means to allow the blend to be subjected to a shearing action such as, for example, by rocking action or mechanical agitation such as using a slow speed stirrer, and to simultaneously subject the blend to vibration, all while a vacuum is being applied. These three process steps --evacuating, vibrating and shearing -- are req~ired to be done concurrently and are criti-al within certain broad parameters.
For example, the vacuum should be between about 15 to about 3Q
inches of mercury and the vibration is preferable at about 2,000 to about 4,000 cycles per minute.
The mechanisms of this process are (1) to invoke migration of entrapped air to the surface by means of applying a vacuum and vibration, and (2~ to facilltate release of this air upon its reaching the surface by shearing of the bubbles by some mechanical means~ The latter mechanism is assisted by incorporating into the blend an anti-~oam or air release agent whose function is to reduce the surface tension of the liquid.
The shearing action is accomplished preferably by rocking the vessel gently over a total of about a 60 degree arc as measured rom a line perpendicular to the horizontal plane of the blend.
A preferred embodlment also includes performing the shearing step by inserting into the blend a baffle comprising a series of fingers between which the blend passes as it is being rocked.
~2~6~22 rhe just-described eva(uatirlg, vlbrating and shearing are critical as to co~bination. That is, all are required simultaneously. !10wever, there ls permissible variation as to the time and quantum. These steps will effectively remove entrapped air which heretofore has been ineffectively removed by other process steps or by the use of degassing or defoaming chemical agents.
After thls pretreatment step, it is generally necessary to vibrate the blend agaln. This vibrating step is accomplished without any accompanying evacuation or shearing and is merely for the purpose of re-incorporating devolved volatiles such as styrene monomer, the entrapped alr now being no longer present.
This last process step can be accomplished after the blend has been poured into a mold, in which case the vibrator is merely attached to the mold's exterior surface.
The afore~entioned pretreating process produces a blend which may be utilized in all conventional casting processes and will produce a cured rigid material, or part, which is substantially void free in cross section. This means that cast marble, which has heretofore been limited to uses as bathroom sinks, table tops, lamps, etc. which are totally precast and merely installed in the Field, can now be expanded to such applications as countertops for kitchens, bars, etc. wher~ the material to be used must be cu. to fit on the job site.
The cast marble produced by the pretreating process of this invention is pleasing to the eye in cross section and inherently stronger due to the absence of voids in the material.
BRIEF DESCRIPTION OF THE DRA~ING(S) Figure l is a flow diagram showing the process steps of this lnvention~
Figure 2 illustrates as a s~hematic~ drawing, a preferred embodiment of the concur~ently performed shearing, vibrating and evacuating step.
Figure 3, a front vlew taken along lines 3--3 of Eigure 2, shows, in longitudinal cross section, an evacua~ing vessel containing a baffle suitable for use in the process of this invention.
DETAILED DESCRIPTION OF TH~ PREFERRED EMBODIMENT(S) Referring now to the drawings, and more particularly to Figure 1 and at arrow 10, the words "to mlxer" are intended to indicate the formulation of a liquid thermosetting polyester resin in a typical batch mlxture as lndicated in Example I
below:
Exam~le I
,'J 300 grams of polyester resin; 1,200 cp; Silman 585 brand ,,r; ~
700 grams of calclum carbonate filler; 325 mesh Pfizer FGD brand grams of 50 percent methyl ethyl ketone peroxide;
Superox 709 Reichold Chemicals brand are mlxed together. Up to 200 parts per mlllion of poly dimethyl siloxane, Union Carbide SAG 100 may be added, if desired~ Any larger amount is not required and the siloxane may be eliminated altogether. The resulting mixture is blend-ed as indi~ated at step 12 for about five minutes or as long as needed to thoroughly blend the mix. The mix is then transferred as indicated by arrow 14 to a vacuum vessel as indicated at block 16. The vacuum vessel is preferably a rocking vessel capable of til~lng at least 30 degrees from vertical in each direction for ~ lr~ k ~Z~6822 a total arc o~ rotation of 60 degrees. The vessel includes means to induce rocking at a frequenc~y oF one to two cycles per minute during the evacuation cycle. Addltionally, a vibrator is attached to the vessel to induce a vibration cycle of From about 2,00~ to about 4,000 cycles per minute.
The combined steps o~ evacuatlon, vibration and shearing are performed for about thirty minutes which for a mix of this volum~ has been found su FFicient to rupture and rel~ase substantially all the entrapped air.
This shearing action thus des~ribed is facilitated by placing, in the vessel prior to the sealing and evacuation, a baffle consisting of a linear series of fingers which extend into the blend so that the blend must pass between the fingers during the rocking cycle.
Following completion of the thirty minute evacuating, shearing and vibrating step, the vessel is opened, a pigment or colorant such as two ounces of titanium dioxide are added to the blend, as is conventional in this art, and the blend, or matrix, is then transferred as indicated at arrow 18 to a mold.
~ fter the blend is poured or trowled into a mold (which may be prepared with a gel coat, etc. as is well known in the art~, the mold is vibrated, again at about 2,000 to 4,000 cycles per minute, for a period o~ about 15 minutes to facilitate redisolving of styrene monomer. At this step in the process, it is important to note that vibration is not for the purpose of releasing air, in as much as little or no air is left, and the vibration at this point would be ineffective for this purpose anyway, as the prior art makes clear. That is, vibration as indicate~ by step 21 in Figure 1 is for the sole purpose of re-incorporating the devolved volatiles such as styrene monomer ~2~682;~
back into ~he hlend. Devolving styrene can be readily seen by surface bubble formation and the vibrating step may be eliminated if no devolving takes place.
Referring now to Figure 2, the critical combination step of evac~uating, shearing and vlbrating step is shown schematically. In Flgure 2, vessel 20 is shown diagramatically to bett*r illustrate the shearing process. In Figure 2, vessel is shown first at rest as indicated by lead line 22 and showing blend 24 at rest> Also shown in Figure 2 are two additional positions of vessel 20, both illustrated in phantom and each showing a 30 degree arc as indicated by arrow 26.
Thus, the total ar- of rocking of vessel 20 is 60 degrees as lndicated by arrow 28.
Also shown in cross section in Figure 2 is baffle 30 which is better illustrated by reference now to Figure 3, In Figure 3, taken along lines 3--3 of Figure 2, vessel 20 is shown in cross section again but with baffle 30 shown in front elevation, including fingers 32 between which blend 24 passes during the rocking of vessel 20 which gives rise to the shearing step of the process as previously desc~ribed.
Following the completion of the shearing, evacuating and vibrating step, vessel 20 is opened. ~t this point, the colorants or pigments as previously described in Example I are added. Blend 2¢ is now transferred to a previo~sly prepared mold as indicated at arrow 18 in Figure 1, and which has prevlously been describecl including a gel coating applied in the conventional manner.
There are many variations which may be practiced within the scope of this invention. For example, while described and illustrated as a batch process, th* process steps may be ~2~682Z
co~ined Wi.ttl d continlJous coatiny process.
Also, although illustrated as a casting process, since the process of this invention ls dir~cted to pre-casting, the part forming step itself is not limited to casting, but is also suitable for injection ~olding as well as all other part ~orming steps.
Also, this invention ls not llmlted to a rigid mold. A
nonrigid, or flexible, mold such is common for decorative items like lamp bases may be used, or parts may be cast ln flexlble molds using wood fillers such as is common for furniture parts.
It should be noted that clear casting resins without fillers may be used such as is common for decorative items.
There are many advantages to the pre-treatment process of this invention. Chiefly is the ability to manufacture cast marble items or parts which are nonporous and, thus, may be machined or cut to leave an exposed edge which is pleasing to the eye. The use of lnexpensive mechanical process steps eliminates the need for expensive, and largely ineffective, chemical degassing additives.
Improved physical properties including greater tensile strength (resistance to thermal and mechanical stresses) and greater bond strength between the matrix and the gel coat are additional advantages achieved by the use of the process of this invention.
Having now illustrated and described my invention, it is not intended that such description limit this invention, but rather that this invention be limited only a reasonable interpretation of the apended Claims.
Claims (13)
1. A process for producing a cast polyester resin comprising the following steps in serial order:
(a) formulating a mixture of liquid thermosetting unsaturated polyester resin, including cross-linking monomer and catalyst to form a blend;
(b) subjecting said blend to a vacuum within predetermined parameters of time and quantum while concurrently vibrating and shearing said blend to rupture and release entrapped air bubbles; and, (c) vibrating said blend while it is in the mold to re-incorporate devolved volatiles to form a matrix capable of setting and curing to form nonporous, machinable cast marble.
(a) formulating a mixture of liquid thermosetting unsaturated polyester resin, including cross-linking monomer and catalyst to form a blend;
(b) subjecting said blend to a vacuum within predetermined parameters of time and quantum while concurrently vibrating and shearing said blend to rupture and release entrapped air bubbles; and, (c) vibrating said blend while it is in the mold to re-incorporate devolved volatiles to form a matrix capable of setting and curing to form nonporous, machinable cast marble.
2. The process according to Claim 1 wherein said vacuum, shearing and vibrating time of step (b) is about thirty minutes.
3. The process according to Claim 1 wherein said vacuum of step (b) is in the range of fifteen to about thirty inches of mercury.
4. The process according to Claim 1 wherein said shearing of step (b) is accomplished by subjecting said blend to a constantly changing horizontal plane.
5. The process according to Claim 4 wherein said constantly changing horizontal plane is provided by rocking said blend over about a 60 degree arc.
6. The process according to Claim 1 wherein shearing of step (b) is accomplished by subjecting said blend to passage through a baffle comprising a series of fingers placed in said blend perpendicular to said horizontal plane.
7. The process according to Claim 1 wherein said process is performed as a batch process.
8. The process according to Claim 1 wherein said process is performed as a continuous process.
9. The process according to Claim 1 wherein said formulation of step (a) comprises about twenty to about forty weight percent of polyester resin characterized by a viscosity of from about 600 to about 3000 centipoise, and wherein said resin cross-linking monomer is styrene, and containing, additionally, a filler selected from the group consisting of calcium carbonate, glass frit, aluminum trihydrate and combinations thereof and wherein said filler is from about seventy to about eighty weight percent and passes a three hundred twenty-five mesh and, further, wherein said formulation includes, as a catalyst, about one weight percent of fifty percent methyl ethyl ketone peroxide.
10. The process according to Claim 9 wherein said mix includes, additionally, a defoaming agent and wherein before step (c) a pigment is added.
11. A process for pretreating castable polyester resin comprising the following serial steps:
(a) formulating and blending a mixture of from about twenty to about thirty weight percent, twelve hundred centipoise liquid propylene glycol esterified with adipic and maleic anhydride, unsaturated polyester resin including styrene as a cross-linking monomer, from about seventy to about eighty weight of a filler selected from the group consisting of calcium carbonate and aluminum trihydrate of about three hundred twenty-five mesh and no more than about two hundred parts per million by weight of dimethyl polysiloxane as a defoamer and about one weight percent of fifty percent methyl ethyl ketone peroxide as a catalyst;
(b) subjecting said blend to a vacuum of from about fifteen to about twenty-five inches of mercury for about thirty minutes while concurrently rocking said blend by tilting said blend over a total of about a 60 degree arc as measured from a line perpendicular to said horizontal plane at about one to two cycles per minute, all while vibrating said blend at about two thousand to four thousand cycles per minute to rupture and release entrapped air bubbles to form a mold ready matrix;
(c) introducing said matrix into a prepared mold;
(d) vibrating said mold at from about two thousand to about four thousand cycles per minute for a period of about fifteen minutes to re-incorporate devolving styrene; and, (e) allowing said blend to set and cure to form a nonporous, machinable cast marble molded part.
(a) formulating and blending a mixture of from about twenty to about thirty weight percent, twelve hundred centipoise liquid propylene glycol esterified with adipic and maleic anhydride, unsaturated polyester resin including styrene as a cross-linking monomer, from about seventy to about eighty weight of a filler selected from the group consisting of calcium carbonate and aluminum trihydrate of about three hundred twenty-five mesh and no more than about two hundred parts per million by weight of dimethyl polysiloxane as a defoamer and about one weight percent of fifty percent methyl ethyl ketone peroxide as a catalyst;
(b) subjecting said blend to a vacuum of from about fifteen to about twenty-five inches of mercury for about thirty minutes while concurrently rocking said blend by tilting said blend over a total of about a 60 degree arc as measured from a line perpendicular to said horizontal plane at about one to two cycles per minute, all while vibrating said blend at about two thousand to four thousand cycles per minute to rupture and release entrapped air bubbles to form a mold ready matrix;
(c) introducing said matrix into a prepared mold;
(d) vibrating said mold at from about two thousand to about four thousand cycles per minute for a period of about fifteen minutes to re-incorporate devolving styrene; and, (e) allowing said blend to set and cure to form a nonporous, machinable cast marble molded part.
12. A cast polyester resin, said resin produced by:
(a) formulating a mixture of liquid thermosetting unsaturated polyester resin, including cross-linking monomer and catalyst to form a blend;
(b) subjecting said blend to a vacuum within predetermined parameters of time and quantum while concurrently vibrating and shearing said blend to rupture and release entrapped air bubbles;
(c) molding said blend;
(d) vibrating said blend while in the mold to re-incorporate devolved volatiles; and, (e) allowing said blend to set and cure while in said mold to form thereby a nonporous, machinable cast marble.
(a) formulating a mixture of liquid thermosetting unsaturated polyester resin, including cross-linking monomer and catalyst to form a blend;
(b) subjecting said blend to a vacuum within predetermined parameters of time and quantum while concurrently vibrating and shearing said blend to rupture and release entrapped air bubbles;
(c) molding said blend;
(d) vibrating said blend while in the mold to re-incorporate devolved volatiles; and, (e) allowing said blend to set and cure while in said mold to form thereby a nonporous, machinable cast marble.
13. A cast polyester resin produced by the following serial steps:
(a) formulating and blending a mixture of from about twenty to about thirty weight percent, twelve hundred centipoise liquid propylene glycol esterified with adipic and maleic anhydride, unsaturated polyester resin including styrene as a cross linking monomer, from about seventy to about eighty weight of a filler selected from the group consisting of calcium carbonate and aluminum trihydrate of about three hundred twenty-five mesh, and no more than about two hundred parts per million by weight of dimethyl polysiloxane as a defoamer, and about one weight percent of fifty percent methyl ethyl ketone peroxide as a catalyst;
(b) subjecting said blend to a vacuum of from about fifteen to about twenty-five inches of mercury for about thirty minutes while concurrently rocking said blend by tilting said blend over a total of about a 60 degree arc as measured from a line perpendicular to said horizontal plane at about one to two cycles per minute, all while vibrating said blend at about two thousand to four thousand cycles per minute to rupture and release entrapped air bubbles to form a mold ready matrix;
(c) introducing said matrix into a prepared mold;
(d) vibrating said mold at from about two thousand to about four thousand cycles per minute for a period of about fifteen minutes to re-incorporate devolving styrene; and, (e) allowing said blend to set and cure to form a nonporous, machine cast, molded part.
(a) formulating and blending a mixture of from about twenty to about thirty weight percent, twelve hundred centipoise liquid propylene glycol esterified with adipic and maleic anhydride, unsaturated polyester resin including styrene as a cross linking monomer, from about seventy to about eighty weight of a filler selected from the group consisting of calcium carbonate and aluminum trihydrate of about three hundred twenty-five mesh, and no more than about two hundred parts per million by weight of dimethyl polysiloxane as a defoamer, and about one weight percent of fifty percent methyl ethyl ketone peroxide as a catalyst;
(b) subjecting said blend to a vacuum of from about fifteen to about twenty-five inches of mercury for about thirty minutes while concurrently rocking said blend by tilting said blend over a total of about a 60 degree arc as measured from a line perpendicular to said horizontal plane at about one to two cycles per minute, all while vibrating said blend at about two thousand to four thousand cycles per minute to rupture and release entrapped air bubbles to form a mold ready matrix;
(c) introducing said matrix into a prepared mold;
(d) vibrating said mold at from about two thousand to about four thousand cycles per minute for a period of about fifteen minutes to re-incorporate devolving styrene; and, (e) allowing said blend to set and cure to form a nonporous, machine cast, molded part.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US492,575 | 1983-05-09 | ||
US06/492,575 US4473673A (en) | 1983-05-09 | 1983-05-09 | Cast polyester resin process and product |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1246822A true CA1246822A (en) | 1988-12-20 |
Family
ID=23956795
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000453791A Expired CA1246822A (en) | 1983-05-09 | 1984-05-08 | Process for pre-treating castable polyester resin |
Country Status (1)
Country | Link |
---|---|
CA (1) | CA1246822A (en) |
-
1984
- 1984-05-08 CA CA000453791A patent/CA1246822A/en not_active Expired
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