Method and apparatus for continuous production of partially polymerized compositions and polymers therefrom

Information

  • Patent Grant
  • 8329079
  • Patent Number
    8,329,079
  • Date Filed
    Monday, April 20, 2009
    15 years ago
  • Date Issued
    Tuesday, December 11, 2012
    11 years ago
Abstract
Methods and apparatus for continuous production of a partially polymerized composition according to the invention comprise those that facilitate continuously providing polymerizable composition comprising one or more monomers to an angled plane at an elevated position thereon; irradiating the polymerizable composition to form the partially polymerized composition; and continuously removing the partially polymerized composition from the angled plane at a lower position thereon, wherein the angle of the angled plane facilitates free flow of polymerizing composition from the elevated position to the lower position.
Description
BACKGROUND OF THE INVENTION

The present invention relates generally to a method and apparatus for continuous production of partially polymerized compositions and polymers therefrom.


Polymers form the basis for many important materials. For example, adhesives are one important type of material typically based on polymers. Adhesives can be provided in various forms for application, often depending on how polymers on which they are based are themselves formed. For example, polymer-based adhesives can be prepared and provided in organic solvent for application, after which time the solvent is removed. Polymer-based adhesives can also be prepared and applied without use of organic solvent—for example, as in the case of hot-melt adhesives (i.e., where the adhesive is substantially polymerized prior to its application to a substrate) or web-polymerized adhesives (i.e., where the adhesive is substantially polymerized after its application to a substrate).


Methods for preparation of polymers and materials (e.g., adhesives) based thereupon can be performed in a continuous or batch-wise manner. In contrast to continuous web-polymerized methods, conventional methods of batch polymerization of adhesives and methods of continuous production of hot-melt adhesives typically involve running of an initial polymerization reaction to at least near complete conversion, and often complete conversion, of the monomer to polymer. In both cases, the adhesive is substantially polymerized prior to its application to a substrate as compared to web-polymerized adhesives (i.e., where the adhesive is substantially polymerized after its application to a substrate, as discussed above).


Nevertheless, in order for a polymerizable composition to be capable of forming and maintaining an adequate coating (i.e., a cohesive coating) for web-polymerization, it is known to be desirable to partially polymerize the composition before forming the coating on-web. See, for example, U.S. Pat. No. 6,866,899, for a discussion of partially polymerized syrup formation when coating a composition onto a substrate for polymerization. Although the web-polymerization itself may be a continuous process, formation of such a syrup is typically a batch process, with the syrup being prepared in a batch polymerization reactor. See, for example, U.S. Pat. Nos. 4,181,752 and 4,303,485. In addition to process inefficiencies inherent in batch processes as opposed to continuous processes, however, conventional batch processing has other disadvantages.


For example, U.S. Pat. No. 7,119,128 discusses the problem of achieving adequate distribution of free radicals generated by ultraviolet radiation throughout a batch polymerization reactor due to limited depth of penetration of ultraviolet radiation therein. In order to assist in overcoming this problem, stirrers and/or other equipment modifications are generally required to be used in such batch polymerization reactors.


U.S. Pat. No. 7,015,295 discusses the difficulty in adequately controlling batch polymerization reactions due to the large exotherm produced upon generation of free radicals when using thermal radiation. In order to assist in overcoming this problem, certain polymerization initiators and processing temperatures must be used according to the methods therein.


Thus, alternative processing methods for web-polymerization and formation of syrups for polymerization on-web are desirable. In addition to the need for alternative processing methods, a need for alternative processing equipment also exists.


While most conventional polymer processing equipment for continuous processes is configured to be substantially horizontal, it is known to utilize a vertical or elevated equipment configuration. German Patent No. 880938 discloses a method of continuous emulsion or suspension polymerization where a vertical tube with partial or continuous agitation is utilized for the select polymerization reactions therein.


U.S. Pat. No. 4,089,918 describes a process for the continuous casting of liquid polymerizable compositions. The compositions are polymerized via thermal polymerization. According to the process described therein, monomer is first partially polymerized and then further polymerized to a degree of polymerization of about 40-60% between a pair of moving belts. The path of the moving belts from a point where the polymerizable composition is inserted therebetween may be straight in a horizontal direction, inclined at a suitable angle to the horizontal, or curved to follow a natural curvature that may be defined by the moving belts when arranged so as to be inclined at a suitable angle to the horizontal.


Nevertheless, in view of environmental and safety concerns as well as the ever-present desire to optimize production efficiency, alternative methods and apparatus for production of further partially polymerized compositions, such as those on which many adhesives are based, are desirable. Particularly desired are alternative methods and apparatus for the continuous production of partially polymerized compositions as well as polymers therefrom.


BRIEF SUMMARY OF THE INVENTION

A method for continuous production of a partially polymerized composition according to the invention comprises: providing an angled plane; continuously providing polymerizable composition comprising one or more monomers to the angled plane at an elevated position thereon; irradiating the polymerizable composition to form the partially polymerized composition; and continuously removing the partially polymerized composition from the angled plane at a lower position thereon, wherein the angle of the angled plane facilitates free flow of polymerizing composition from the elevated position to the lower position.


Similarly, an apparatus for continuous production of a partially polymerized composition according to the invention comprises: an angled plane; an elevated position on the angled plane for continuous receipt of polymerizable composition comprising one or more monomers; at least one radiation source for irradiating the polymerizable composition to form the partially polymerized composition; and a lower position on the angled plane for continuous removal of the partially polymerized composition from the angled plane, wherein the angle of the angled plane facilitates free flow of polymerizing composition from the elevated position to the lower position.


Advantageously, according to preferred embodiments of methods and apparatus of the invention, polymerizing composition undergoes free flow from the elevated position to the lower position of the angled plane. In one embodiment, angle of the angled plane is about 5 degrees to about 90 degrees to horizontal. In a further embodiment, angle of the angled plane is about 20 degrees to about 70 degrees to horizontal. In yet a further embodiment, angle of the angled plane is about 30 degrees to about 60 degrees to horizontal. The angled plane may comprise one or more individual angled sections.


In a further embodiment, methods and apparatus of the invention further comprises providing an upper plate for sandwiching polymerizing composition between the angled plane and the upper plate.


A variety of polymerization mechanisms can be adapted according to the invention. In one embodiment, continuous polymerization of the polymerizable composition proceeds via a free radical mechanism. Partial polymerization can be effected by irradiation of the polymerizable composition using, for example, ultraviolet radiation and/or thermal radiation. In one embodiment, the polymerizing composition is irradiated through at least the angled plane. In another embodiment, the polymerizing composition is irradiated through at least the upper plate.


The partially polymerized composition may comprise a variety of chemistries. In an exemplary embodiment, the partially polymerized composition comprises (meth)acrylate syrup. No matter what type of chemistry comprises the partially polymerized composition, advantageously methods of the invention are essentially solvent-free in preferred embodiments.


According to a further embodiment of the invention, the invention further comprises continuously forming at least one of the one or more monomers to be partially polymerized from one or more precursors thereof. The partially polymerized composition is then formed to the desired percent monomer conversion. In an exemplary embodiment, partially polymerized composition according to the invention comprises about 5% to about 25% monomer conversion.





BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS


FIG. 1A is a schematic representation of one embodiment of an angled plane and associated apparatus for continuous production of partially polymerized compositions according to the present invention, wherein partial polymerization occurs between two plates.



FIG. 1B is a schematic representation of another embodiment of an angled plane and associated apparatus for continuous production of partially polymerized compositions according to the present invention, wherein partial polymerization occurs on the angled plane without the presence of an upper plate on the polymerizing composition.



FIG. 1C is a schematic representation of yet another embodiment of an angled plane and associated apparatus for continuous production of partially polymerized compositions according to the present invention, wherein partial polymerization occurs on an angled plane comprising multiple discontinuous plates.



FIG. 1D is a schematic representation of a further embodiment of an angled plane and associated apparatus for continuous production of partially polymerized compositions according to the present invention, wherein the partially polymerized composition departs the angled plane and continues onto a moving web for further polymerization.



FIG. 1E is a schematic representation of another embodiment of an angled plane and associated apparatus for continuous production of partially polymerized compositions according to the present invention, wherein polymerizing composition is irradiated through the angled plane.



FIG. 1F is a schematic representation of yet another embodiment of an angled plane and associated apparatus for continuous production of partially polymerized compositions according to the present invention, wherein partial polymerization occurs between two plates and polymerizing composition is irradiated through the angled plane and an upper plate.





DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to a method and apparatus for continuous production of partially polymerized compositions and, optionally, polymers therefrom. Partial polymerization occurs according to the invention using apparatus comprising an angled plane. According to the invention, a polymerizable composition flows onto the angled plane at an elevated position, flows downward along the plane during partial polymerization thereof, and then exits as a syrup at a lower position on the angled plane.


The present specification makes reference to terms that are described below for convenience of the reader.


As used herein, “(meth)acrylate” refers to both methacrylate and acrylate.


As used herein, “(meth)acrylic acid” refers to both methacrylic acid and acrylic acid.


As used herein, “continuous” refers to a process that is essentially uninterrupted in time and space from a beginning reference point to an ending reference point. In an exemplary embodiment, continuous processes enabled by apparatus of the invention have a beginning reference point corresponding to the point at which monomer is provided to the apparatus for at least partial polymerization and an ending reference point that is no earlier in the process than the point at which a partially polymerized composition, such as a (meth)acrylate syrup, is formed therefrom.


As used herein, “syrup” refers to a partially polymerized composition comprising a mixture of at least one monomer and the polymerization product thereof.


As used herein, “complete conversion” means about 100% of the stoichiometric amount of reactants are reacted, or converted, into their reaction product (i.e., polymer). This percentage of available reactants does not include amounts exceeding stoichiometric quantities of any of the reactants necessary to produce the polymer under the reaction conditions.


As used herein, “near complete conversion” means at least about 90% of the stoichiometric amount of reactants are reacted, or converted, into their reaction product (i.e., polymer). This percentage of available reactants does not include amounts exceeding stoichiometric quantities of any of the reactants necessary to produce the polymer under the reaction conditions.


As used herein, “essentially solvent-free” refers to compositions and associated methods comprising no more than about 5% organic solvents or water, more typically no more than about 3% organic solvents or water. Most typically, such systems are completely free of organic solvents and water.


According to the invention, a polymerizable composition (hereinafter interchangeably referred to as “monomer” for simplicity, whether or not the composition is partially polymerized to a degree) is provided to apparatus of the invention for at least partial polymerization thereof. Any suitable monomer can be used according to the invention. Many stock monomers are readily available from commercial suppliers. Monomer can also be prepared for use in the present invention using methodology known to those of ordinary skill in the art.


In one embodiment of the invention, unlike conventional methods and associated apparatus for polymerization of stock monomers, methods and apparatus of the invention facilitate continuous processing beginning with formation of at least one monomer from precursors thereof as described in co-pending U.S. patent application Ser. No. 12/264,602, entitled “Method For Continuous Production Of (Meth)Acrylate Syrup And Adhesives Therefrom.” Any suitable chemistries and associated precursors can be used to form the monomer or combinations thereof. According to this embodiment, once formed, monomer continues to be processed to a partially polymerized composition in apparatus and according to methodology of the present invention.


In contrast to conventional batch and many continuous polymerization techniques and apparatus, continuous polymerization of monomer does not proceed to complete conversion during partial polymerization thereof when using apparatus according to the invention. Partial polymerization proceeds to the point at which syrup of the desired viscosity is obtained. In part due to configuration of apparatus for partial polymerization according to the invention, polymerization reactions therein are halted at a point prior to complete conversion, and even at a point prior to near complete conversion, of the monomer. Preferably, the polymerization reaction is halted at a point prior to 90% conversion, more preferably at a point prior to 70% conversion, even more preferably at a point corresponding to less than about 45% conversion, yet even more preferably at a point corresponding to about 5% to about 25% conversion, and still even more preferably at a point corresponding to about 5% to about 15% conversion, of the monomer based on molar weight of the monomer. In an exemplary embodiment, desired viscosity of the partially polymerized composition is that viscosity at which the syrup is readily able to flow onto and form a stable coating on a substrate—i.e., a coatable viscosity. Apparatus of the invention are preferably flexibly adapted to accommodate desired results in that regard.


According to one embodiment of the invention, a partially polymerized composition (e.g., (meth)acrylate syrup) comprising a coatable viscosity (i.e., a coatable composition) is capable of being formed continuously and, thus, efficiently. In order to form a cohesive coating, a coatable composition generally must have a sufficiently high viscosity. Yet, it is also important that the coatable composition has a low enough viscosity so that it can readily flow through the partial polymerization apparatus and onto a substrate upon coating. In an exemplary embodiment, coatable compositions formed according to the invention have a Brookfield viscosity of about 0.2 Pascal-second (200 centipoise) to about 10 Pascal-seconds (10,000 centipoise) when measured at room temperature. A composition's Brookfield viscosity is measurable using equipment and according to methodology known to those of ordinary skill in the art. For example, a rotational viscometer such as those available from Cole-Parmer (Vernon Hills, Ill.) can be used to measure a composition's Brookfield viscosity.


In one embodiment, coatable compositions formed according to the invention have a Brookfield viscosity of about 5 Pascal-seconds (5,000 centipoise) or less when measured at room temperature. In another embodiment, coatable compositions formed according to the invention have a Brookfield viscosity of about 4 Pascal-seconds (4,000 centipoise) or less when measured at room temperature. For example, coatable compositions formed according to the invention can have a Brookfield viscosity of about 0.5 Pascal-second (500 centipoise) to about 5 Pascal-seconds (5,000 centipoise) when measured at room temperature. As yet another example, coatable compositions formed according to the invention can have a Brookfield viscosity of about 1 Pascal-second (1,000 centipoise) to about 3 Pascal-seconds (3,000 centipoise) when measured at room temperature.


Partial polymerization of the monomer to form the coatable composition can be effected using any suitable polymerization mechanism. Exemplary polymerization mechanisms include free radical polymerization, anionic polymerization, and cationic polymerization. Depending on the type of monomer and polymerization mechanism, polymerization initiators may be desired or required. Polymerization initiators are also selected, in part, based on the energy source to be used during polymerization. Any suitable energy source can be used according to the invention. Exemplary energy sources include actinic radiation (e.g., ultraviolet radiation or e-beam) and thermal radiation sources. Any polymerization initiators used can be mixed with the monomer prior to or during the partial polymerization thereof as known to those skilled in the art in order to effectuate the desired polymerization.


In addition to polymerization initiators, other suitable additives can be included in the polymerizable composition as desired and selected in types and amounts as known to those skilled in the art. According to the invention, however, preferably the partial polymerization proceeds in an essentially solvent-free manner. Advantageously, the absence of solvents (i.e., both organic solvents and water) allows smaller and less costly reaction equipment to be used for that stage. In contrast, as discussed in the background of the invention above, safety mandates that relatively large and specially designed reaction equipment be utilized for conventional solvent-based batch polymerization in order to accommodate the large reaction exotherm and solvents. The solvents must also then be removed, which negatively impacts process efficiency.


In an exemplary embodiment, partial polymerization according to the invention proceeds via free radical polymerization initiated using a radiation source, such as an ultraviolet energy radiation source. The amount and intensity of irradiation from the radiation source is adjusted according to the knowledge of those of ordinary skill in the art to obtain the desired resulting polymer properties. The spectral distribution of the radiation together with the rate of irradiation is known to substantially control the rate of polymerization. The rate of polymerization, in turn, determines the molecular weight of the resulting polymer. The molecular weight of the polymer and the choice of the monomers are among the factors that ultimately determine the resulting polymer's properties.


As noted above and with reference to FIG. 1A, monomer flows onto an angled plane 102 at an elevated position in partial polymerization apparatus of the invention. Then, the monomer flows downward in direction 104 along the angled plane 102 during partial polymerization thereof, after which time it departs as a syrup at a lower position on the angled plane 102. An optional upper plate 108 and radiation source comprising an ultraviolet light bank 112, both further described below, are also illustrated in FIG. 1A.


Angle 106 of the angled plane 102 is selected according to, amongst other considerations: length of the angled plane 102; whether the angled plane 102 comprises one or more individual angled sections 114, 118; and, the length of each angled section 114, 118. Preferably, angle 106 of the angled plane 102 is one that facilitates free flow (i.e., flow without application of non-gravitational force, such as that supplied by mechanical rollers, belts, and the like) of the polymerizing composition from the elevated position to the lower position and at the rate necessary to obtain desired properties in the resulting polymer. The angled plane 102 is also preferably smooth and planar to promote free flow thereon.


In an exemplary embodiment, angle 106 is about 5 degrees to about 90 degrees to horizontal. In a further embodiment, angle 106 is about 10 degrees to about 75 degrees to horizontal. In yet a further embodiment, angle 106 is about 20 degrees to about 70 degrees to horizontal. In still a further embodiment, angle 106 is about 30 degrees to about 60 degrees to horizontal.


Advantageously, providing an angled plane 102 according to the invention facilitates controlled free flow of monomer thereon during partial polymerization thereof. Thus, the invention advantageously eliminates the need for costly and/or complicated apparatus otherwise required to promote adequate conveyance of polymerizing composition along the angled plane 102. To accommodate different applications, in a preferred embodiment the angle 106 of the angled plane 102 is readily adjustable during or between uses of the apparatus. It is also to be understood that the angled plane 102 may comprise multiple angled sections of varying individual section angles.


That is, in all embodiments, the plate comprising angled plane 102 may itself comprise one or more individual plates or layers. As illustrated in FIGS. 1A-1B, the angled plane 102 is essentially one continuous plate. Alternatively, as illustrated in FIG. 1C, the angled plane 102 is discontinuous, comprising multiple angled sections. First angled section 114 of the angled plane 102 has a first length and first angle 116 with respect to horizontal. Second angled section 118 of the angled plane 102 has a second length and second angle 120 with respect to horizontal. While two angled sections 114 and 118 are illustrated in FIG. 1C, more than two angled sections may be present in further embodiments of the invention. While angles 116, 120 of individual angled sections 114, 118 may all vary in such embodiments, understand that two or more individual angled sections 114, 118 in an angled plane 102 comprising multiple angled sections 114, 118 may comprise the same angle 116, 120.


From an alternative perspective, dimensions (e.g., length and width) of the angled plane 102 are selected such that polymerizing composition flows from the elevated position to the lower position of the angled plane 102 at the desired flow rate. Flow rate generally has a material mass component and a time component. Among other possible factors relevant to flow rate, length, width and thickness of the polymerizing composition correspond to the material mass flow rate component. Likewise, among other possible factors relevant to flow rate, angle 106 and viscosity of the polymerizing composition correspond to the time flow rate component.


Thickness of the polymerizing composition is generally dependent on and/or adjusted based on chemistry of the polymerizable composition; the degree of partial polymerization (i.e., percent conversion) desired; the type of radiation used to initiate polymerization of the polymerizable composition; and, properties desired in the resulting material. In an exemplary embodiment of the invention, thickness of the polymerizing composition does not significantly impact flow rate thereof.


Generally to a much greater extent according to an exemplary embodiment of the invention, flow rate is dependent on, among other factors (e.g., angle 106), aspect ratio of the polymerizing composition. It is to be understood that “aspect ratio” of the polymerizing composition is the ratio of a film of the polymerizing composition's longest dimension to its next longest dimension. While aspect ratio is defined in terms of dimensions of the polymerizing composition, it is to be understood that dimensions of the polymerizing composition are related to dimensions of the angled plane 102. For example, length of the angled plane 102 approximates length of the polymerizing composition downward along the angled plane 102 and width of the angled plane 102 is at least the width of the polymerizing composition.


In one embodiment, aspect ratio of the polymerizing composition is the ratio of its length to its width. Aspect ratio of the angled plane 102 (and any individual angled sections 114, 118 of the angled plane 102 when it is discontinuous according to further embodiments) is selected according to, amongst other considerations, the angle 106 of the angled plane 102; whether the angled plane 102 comprises one or more individual angled sections 114, 118; the length of each individual angled section 114, 118; the width of each individual angled section 114, 118; and, the angle 116, 120 of each angled section 114, 118.


In an exemplary embodiment, aspect ratio of the polymerizing composition is about 1:1 to about 100:1. In a further embodiment, aspect ratio of the polymerizing composition is about 2:1 to about 50:1. In yet a further embodiment, aspect ratio of the polymerizing composition is about 3:1 to about 25:1.


In one embodiment, partial polymerization is carried out in the absence of air and oxygen (which can inhibit the polymerization reaction). When an inert environment is necessary to effect desired partial polymerization (e.g., when the polymerization mechanism is free radical polymerization as opposed to anionic or cationic polymerization), any suitable mechanism for effecting the inert environment can be used as known to those of ordinary skill in the art. In general, any suitable method for creating an inert environment can be used according to the invention.


In one such embodiment, as also illustrated in FIG. 1A, an inert environment is effected in a portion of the partial polymerization apparatus by sandwiching monomer between two plates—e.g., the angled plane 102 and an upper plate 108—having a relatively small gap therebetween. It is to be understood that each of the two plates 102, 108 may comprise one or more individual plates or layers. Further, the plates 102, 108, which are preferably solid, can be the same or different with respect to the type of material from which they are made and/or their dimensions. While not required, in a further embodiment, the plates 102, 108 or separate side plates (not shown) are configured to also enclose the relatively small gap between sides of the plates 102, 108.


Partial polymerization is effected by irradiating monomer, which flows in direction 104 along angled plane 102, from an elevated position to a lower position thereon, through one or both of the plates 102, 108. Monomer is irradiated as such using a suitable radiation source, for example, an ultraviolet bulb bank 112.


In another embodiment for partially polymerizing in an inert environment, the partial polymerization apparatus is operated within a larger, inert reaction chamber to form an inert environment for partial polymerization. In another such embodiment, an inert environment is effected in a portion of the partial polymerization apparatus by creating a localized inert space 110 over the monomer being partially polymerized on the angled plane 102. In both of these embodiments, as generally illustrated in FIG. 1B, monomer flows in direction 104 along angled plane 102, from an elevated position to a lower position thereon, without being sandwiched by an upper plate.


In an exemplary embodiment, any plate positioned between the radiation source and monomer being partially polymerized on the angled plane 102, such as upper plate 108 illustrated in FIG. 1A, is selected to be of the type facilitating transmission of radiation from the radiation source therethrough. In one embodiment, any suitable transparent or translucent material can be used for any plate positioned between an ultraviolet radiation source and monomer being partially polymerized on the angled plane 102 to allow transmission of ultraviolet radiation therethrough. A wide variety of transparent and translucent materials are known and suitable for this purpose, including many types of glass and plastic. In another embodiment, any plate positioned between a thermal radiation source and monomer being partially polymerized on the angled plane 102 facilitates transmission of thermal radiation therethrough. A wide variety of thermally conductive materials are suitable for this purpose, including most commonly those based on metal.


While the radiation source is illustrated above the angled plane 102 in FIGS. 1A-1D, it is to be understood that the radiation source can be positioned below the angled plane 102 or in other suitable locations as known to those of ordinary skill in the art and depending on the type of polymerization, chemistry of the polymerizable composition, type of plate(s) in the apparatus, and other similar factors. One such embodiment is illustrated in FIG. 1E, where a radiation source comprising an ultraviolet light bank 130 is positioned below the angled plane 102 for irradiation of polymerization composition therethrough. A further embodiment is illustrated in FIG. 1F, wherein the radiation source comprising an ultraviolet light bank 130 is positioned below the angled plane 102 and the radiation source comprising an ultraviolet light bank 112 is also positioned above the angled plane 102.


In an exemplary embodiment, as compared to batch polymerization techniques and associated apparatus, apparatus facilitating continuous methods according to the invention enable efficient formation of a partially polymerized composition by exposing only a relatively small volume of material at a time to reaction conditions during the partial polymerization. This relatively short and low volume reaction advantageously enables a more controlled reaction product and safer reaction conditions, particularly in view of the highly exothermic nature of, for example, the free radically initiated (meth)acrylate polymerization reaction.


Once the partially polymerized composition is formed, it can be stored for later processing or continuously supplied to further processing equipment for additional continuous processing as known to those skilled in the art. As illustrated in FIG. 1D, partially polymerized composition flows from the angled plane 102 onto a web 124 moving in direction 126 for further polymerization on-web. The further polymerized composition exits the web 124 to apparatus 128 for further processing and/or storage.


Process efficiency is optimized when partially polymerized composition flows from the angled plane 102 onto the web 118 for complete, or near complete, conversion of monomer to the desired polymer. Advantageously, apparatus and methods of the invention enable continuous processing of monomer through at least partial polymerization thereof—and from a point prior to formation of the monomer and/or to a point corresponding to formation of polymers from the monomer in further embodiments.


Exemplary embodiments and applications of apparatus of the invention are described in the following non-limiting examples.


EXAMPLES
Example 1

First, 90 parts by weight iso-octyl acrylate and 10 parts by weight acrylic acid were mixed to form a monomer mixture. Then, 0.1% photoinitiator (IRGACURE 819, a bis-acyl-phosphine oxide photoinitiator with a maximum absorption in the range of about 360-390 nanometers, available from Ciba Specialty Chemicals Inc. of Tarrytown, N.Y.) based on weight of the monomer mixture was added to form a polymerizable composition.


Then, two glass plates, each measuring 30 cm×38 cm (12 inches×15 inches), separated by a gap of 1.5 mm (60 mils) were laid out at an angle of 45° to horizontal, the bottom plate comprising an angled plane according to the invention. Above the glass plates, a bank of BLC bulbs were provided at a sufficient intensity (400-450 mJ/cm2, as measured using a UV Map Plus from Electronic Instrumentation & Technology, Inc. of Sterling, Va.) to partially polymerize the polymerizable composition.


To begin polymerization, the gap between the glass plates was inerted using nitrogen. The polymerizable composition was then fed into the inerted gap at a rate of about 20 kg/hr. Upon entering the gap, the composition was allowed to freely flow between the glass plates and partially polymerize, exiting the glass plates with a Brookfield viscosity of about 2,500 cPs (2.5 mPa·sec).


Various modifications and alterations of the invention will become apparent to those skilled in the art without departing from the spirit and scope of the invention, which is defined by the accompanying claims. It should be noted that steps and stages recited in any method claims below do not necessarily need to be performed in the order that they are recited. Those of ordinary skill in the art will recognize variations in performing the steps and stages from the order in which they are recited. In addition, the lack of mention or discussion of a feature, step, stage, or component provides the basis for claims where the absent feature or component is excluded by way of a proviso or similar claim language.


Further, as used throughout, ranges may be used as shorthand for describing each and every value that is within the range. Any value within the range can be selected as the terminus of the range. Similarly, any discrete value within the range can be selected as the minimum or maximum value recited in describing and claiming features of the invention.


In addition, as discussed herein it is again noted that the compositions described herein may comprise all components in one or multiple parts. Other variations are recognizable to those of ordinary skill in the art.

Claims
  • 1. A method for continuous production of a partially polymerized composition, comprising: providing an angled plane;continuously providing polymerizable composition comprising one or more monomers to the angled plane at an elevated position thereon;irradiating the polymerizable composition to form the partially polymerized composition; andcontinuously removing the partially polymerized composition from the angled plane at a lower position thereon,wherein the angle of the angled plane facilitates free flow of polymerizing composition from the elevated position to the lower position, andwherein the method is essentially solvent-free.
  • 2. The method of claim 1, further comprising providing an upper plate for sandwiching polymerizing composition between the angled plane and the upper plate.
  • 3. The method of claim 1, wherein the step of continuously providing polymerizable composition comprising one or more monomers to the angled plane at an elevated position thereon comprises continuously forming at least one of the one or more monomers from one or more precursors thereof.
  • 4. The method of claim 1, wherein the partially polymerized composition comprises (meth)acrylate syrup.
  • 5. The method of claim 1, wherein the partially polymerized composition comprises about 5% to about 25% monomer conversion.
  • 6. A method for continuous production of a partially polymerized composition, comprising: continuously forming at least one monomer from one or more precursors thereof;providing an angled plane;continuously providing polymerizable composition comprising the at least one monomer to the angled plane at an elevated position thereon;irradiating the polymerizable composition to form the partially polymerized composition; andcontinuously removing the partially polymerized composition from the angled plane at a lower position thereon,wherein the angle of the angled plane facilitates free flow of polymerizing composition from the elevated position to the lower position.
  • 7. The method of claim 1, wherein continuous polymerization of the polymerizable composition proceeds via a free radical mechanism.
  • 8. The method of claim 1, wherein the polymerizable composition is irradiated using ultraviolet radiation.
  • 9. The method of claim 1, wherein the polymerizable composition is irradiated using thermal radiation.
  • 10. The method of claim 1, wherein the angle of the angled plane is about 5 degrees to about 90 degrees to horizontal.
  • 11. The method of claim 1, wherein the angle of the angled plane is about 20 degrees to about 70 degrees to horizontal.
  • 12. The method of claim 1, wherein the angle of the angled plane is about 30 degrees to about 60 degrees to horizontal.
  • 13. The method of claim 1, wherein the angled plane comprises one or more individual angled sections.
  • 14. The method of claim 1, wherein the polymerizing composition undergoes free flow from the elevated position to the lower position.
  • 15. The method of claim 1, wherein the polymerizing composition is irradiated through at least the angled plane.
  • 16. The method of claim 2, wherein the polymerizing composition is irradiated through at least the upper plate.
  • 17. The method of claim 6, wherein the method is essentially solvent-free.
  • 18. The method of claim 6, further comprising providing an upper plate for sandwiching polymerizing composition between the angled plane and the upper plate.
  • 19. The method of claim 6, wherein the partially polymerized composition comprises (meth)acrylate syrup.
  • 20. The method of claim 6, wherein the partially polymerized composition comprises about 5% to about 25% monomer conversion.
  • 21. The method of claim 6, wherein continuous polymerization of the polymerizable composition proceeds via a free radical mechanism.
  • 22. The method of claim 6, wherein the polymerizable composition is irradiated using ultraviolet radiation.
  • 23. The method of claim 6, wherein the polymerizable composition is irradiated using thermal radiation.
  • 24. The method of claim 6, wherein the angle of the angled plane is about 5 degrees to about 90 degrees to horizontal.
  • 25. The method of claim 6, wherein the angle of the angled plane is about 20 degrees to about 70 degrees to horizontal.
  • 26. The method of claim 6, wherein the angle of the angled plane is about 30 degrees to about 60 degrees to horizontal.
  • 27. The method of claim 6, wherein the angled plane comprises one or more individual angled sections.
  • 28. The method of claim 6, wherein the polymerizing composition undergoes free flow from the elevated position to the lower position.
  • 29. A method for continuous production of a partially polymerized composition, comprising: continuously forming at least one monomer from one or more precursors thereof;providing an angled plane;continuously providing polymerizable composition comprising the at least one monomer to the angled plane at an elevated position thereon;irradiating the polymerizable composition through at least the angled plane to form the partially polymerized composition; andcontinuously removing the partially polymerized composition from the angled plane at a lower position thereon,wherein the angle of the angled plane facilitates free flow of polymerizing composition from the elevated position to the lower position.
  • 30. The method of claim 6, wherein the polymerizing composition is irradiated through at least the upper plate.
US Referenced Citations (339)
Number Name Date Kind
3154141 Huet Oct 1964 A
3310600 Ziegler et al. Mar 1967 A
3399227 Tapulionis Aug 1968 A
3628918 Beals et al. Dec 1971 A
3728085 Horiguchi et al. Apr 1973 A
3776947 Shimizu et al. Dec 1973 A
3816267 Chuang Jun 1974 A
3821330 Free Jun 1974 A
3914290 Otsuki et al. Oct 1975 A
4009195 Leister et al. Feb 1977 A
4016348 Adams Apr 1977 A
4046718 Mass et al. Sep 1977 A
4089918 Kato et al. May 1978 A
4110521 Barnett et al. Aug 1978 A
4153774 Boettcher et al. May 1979 A
4173719 Tauber et al. Nov 1979 A
4181752 Martens et al. Jan 1980 A
4200145 Underwood Apr 1980 A
4233267 Coker et al. Nov 1980 A
4258204 Banks et al. Mar 1981 A
4280009 Erpenbach et al. Jul 1981 A
4280010 Erpenbach et al. Jul 1981 A
4287317 Kitagawa et al. Sep 1981 A
4303485 Levins Dec 1981 A
4329384 Vesley et al. May 1982 A
4330590 Vesley May 1982 A
4364972 Moon Dec 1982 A
4379201 Heilmann et al. Apr 1983 A
4383093 Shiraki et al. May 1983 A
4391687 Vesley Jul 1983 A
4395525 Fischer et al. Jul 1983 A
4396675 Groff Aug 1983 A
4402914 Eckhoff Sep 1983 A
4404246 Charbonneau et al. Sep 1983 A
4415615 Esmay et al. Nov 1983 A
4421822 Levens Dec 1983 A
4455205 Olson et al. Jun 1984 A
4478876 Chung Oct 1984 A
4480116 Clonce et al. Oct 1984 A
4513039 Esmay Apr 1985 A
4522870 Esmay Jun 1985 A
4554324 Husman et al. Nov 1985 A
4557960 Vernon et al. Dec 1985 A
4563388 Bonk et al. Jan 1986 A
RE32249 Esmay Sep 1986 E
4617367 Watanabe et al. Oct 1986 A
4619867 Charbonneau et al. Oct 1986 A
4619979 Kotnour et al. Oct 1986 A
4695608 Engler et al. Sep 1987 A
4699843 Charbonneau et al. Oct 1987 A
4731273 Bork et al. Mar 1988 A
4737559 Kellen et al. Apr 1988 A
4748061 Vesley May 1988 A
4766023 Lu Aug 1988 A
4777230 Kamath Oct 1988 A
4810523 William et al. Mar 1989 A
4818610 Zimmerman et al. Apr 1989 A
4840756 Ebersole et al. Jun 1989 A
4843134 Kotnour et al. Jun 1989 A
4847137 Kellen et al. Jul 1989 A
4931347 Slovinsky et al. Jun 1990 A
4942001 Murphy et al. Jul 1990 A
4950537 Vesley et al. Aug 1990 A
4959265 Wood et al. Sep 1990 A
4968558 Fisher et al. Nov 1990 A
4985488 Landin Jan 1991 A
4985562 Rossman et al. Jan 1991 A
4988742 Moon et al. Jan 1991 A
4996029 Martin et al. Feb 1991 A
5009224 Cole Apr 1991 A
5024880 Veasley et al. Jun 1991 A
5028484 Martin Jul 1991 A
5034526 Bonham et al. Jul 1991 A
5057366 Husman et al. Oct 1991 A
5089536 Palazzotto Feb 1992 A
5102715 Zetterquist Apr 1992 A
5106560 Duffy et al. Apr 1992 A
5135981 Matsumaru et al. Aug 1992 A
5147698 Cole Sep 1992 A
5147938 Kuller Sep 1992 A
5153323 Rossman et al. Oct 1992 A
5183833 Fisher et al. Feb 1993 A
5187045 Bonham et al. Feb 1993 A
5188808 Lilja et al. Feb 1993 A
5202361 Zimmerman et al. Apr 1993 A
5236560 Drysdale et al. Aug 1993 A
5237355 Kiehne et al. Aug 1993 A
5266402 Delgado et al. Nov 1993 A
5286601 Rossman et al. Feb 1994 A
5308887 Ko et al. May 1994 A
5344691 Hanschen et al. Sep 1994 A
5354597 Capik et al. Oct 1994 A
5354600 Fisher et al. Oct 1994 A
5371560 Kiehne et al. Dec 1994 A
5385772 Slovinsky et al. Jan 1995 A
5386052 Sakakura et al. Jan 1995 A
5387682 Bonham et al. Feb 1995 A
5391406 Ramharack et al. Feb 1995 A
5407717 Lucast et al. Apr 1995 A
5416127 Chandran et al. May 1995 A
5458983 Wang et al. Oct 1995 A
5462797 Williams et al. Oct 1995 A
5462977 Yoshikawa et al. Oct 1995 A
5464659 Melancon et al. Nov 1995 A
5468821 Lucast et al. Nov 1995 A
5496504 Bonham et al. Mar 1996 A
5501679 Krueger et al. Mar 1996 A
5514730 Mazurek et al. May 1996 A
5521227 Palazotto et al. May 1996 A
5521229 Lu et al. May 1996 A
5527595 Slovinsky et al. Jun 1996 A
5536759 Ramharack et al. Jul 1996 A
5559163 Dawson et al. Sep 1996 A
5568210 Kiehne et al. Oct 1996 A
5589246 Calhoun et al. Dec 1996 A
5593795 Chen et al. Jan 1997 A
5602221 Bennett et al. Feb 1997 A
5616670 Bennett et al. Apr 1997 A
5620795 Haak et al. Apr 1997 A
5623000 Yoshikawa et al. Apr 1997 A
5624763 Melancon et al. Apr 1997 A
5624973 Lu et al. Apr 1997 A
5637395 Uemura et al. Jun 1997 A
5637646 Ellis Jun 1997 A
5641544 Melancon et al. Jun 1997 A
5643648 Kobe et al. Jul 1997 A
5643668 Calhoun et al. Jul 1997 A
5650215 Mazurek et al. Jul 1997 A
5654387 Bennett et al. Aug 1997 A
5658630 Shizukuda et al. Aug 1997 A
5660925 Cooley et al. Aug 1997 A
5667893 Kinzer et al. Sep 1997 A
5670260 Zajaczkowski et al. Sep 1997 A
5670557 Dietz et al. Sep 1997 A
5674561 Dietz et al. Oct 1997 A
5679756 Zhu et al. Oct 1997 A
5683798 Bennett et al. Nov 1997 A
5686504 Ang Nov 1997 A
5691034 Krueger et al. Nov 1997 A
5695837 Everaerts et al. Dec 1997 A
5702771 Shipston et al. Dec 1997 A
5708109 Bennett et al. Jan 1998 A
5708110 Bennett et al. Jan 1998 A
5710227 Freeman et al. Jan 1998 A
5725947 Johannson et al. Mar 1998 A
5726258 Fischer et al. Mar 1998 A
5728502 Ou-Yang et al. Mar 1998 A
5734074 Dockner et al. Mar 1998 A
5741542 Williams et al. Apr 1998 A
5741543 Winslow et al. Apr 1998 A
5753362 Kawase et al. May 1998 A
5753768 Ellis May 1998 A
5756584 Bennett et al. May 1998 A
5770219 Chiang et al. Jun 1998 A
5773485 Bennett et al. Jun 1998 A
5779632 Dietz et al. Jul 1998 A
5800685 Perrault Sep 1998 A
5804610 Hamer et al. Sep 1998 A
5811574 Exner et al. Sep 1998 A
5840783 Momchilovich et al. Nov 1998 A
5848769 Fronek et al. Dec 1998 A
5853642 Siedle et al. Dec 1998 A
5853750 Dietz et al. Dec 1998 A
5858516 Ou-Yang Jan 1999 A
5859088 Peterson et al. Jan 1999 A
5871607 Hamilton et al. Feb 1999 A
5879759 Zang Mar 1999 A
5883149 Bennett et al. Mar 1999 A
5883288 Iffland et al. Mar 1999 A
5900125 Exner et al. May 1999 A
5902836 Bennett et al. May 1999 A
5919603 Miyazaki et al. Jul 1999 A
5932298 Moon Aug 1999 A
5942642 Beyer et al. Aug 1999 A
5945560 Iffland et al. Aug 1999 A
5952398 Dietz et al. Sep 1999 A
5965235 McGuire et al. Oct 1999 A
5968633 Hamilton et al. Oct 1999 A
5969069 Su et al. Oct 1999 A
5976690 Williams et al. Nov 1999 A
5980932 Chiang et al. Nov 1999 A
5986011 Ellis Nov 1999 A
6015603 Ou-Yang Jan 2000 A
6030701 Johnson et al. Feb 2000 A
6034263 Rizzardo et al. Mar 2000 A
6037430 Chiang Mar 2000 A
6045920 Ou-Yang et al. Apr 2000 A
6072076 Schmidt et al. Jun 2000 A
6084122 Garza et al. Jul 2000 A
6099940 Hamilton et al. Aug 2000 A
6103316 Tran et al. Aug 2000 A
6123890 Mazurek et al. Sep 2000 A
6124417 Su Sep 2000 A
6126865 Haak et al. Oct 2000 A
6132844 Atshuler et al. Oct 2000 A
6148496 McGuire et al. Nov 2000 A
6149935 Chiang et al. Nov 2000 A
6150486 Schwede et al. Nov 2000 A
6159557 Meyer-Roscher et al. Dec 2000 A
6168682 Bennett et al. Jan 2001 B1
6172170 Koniger et al. Jan 2001 B1
6174931 Moon et al. Jan 2001 B1
6177190 Gehlsen et al. Jan 2001 B1
6187127 Bolitsky et al. Feb 2001 B1
6193918 McGuire et al. Feb 2001 B1
6194062 Hamilton et al. Feb 2001 B1
6214460 Bluem et al. Apr 2001 B1
6217965 Gelbart Apr 2001 B1
6228449 Meyer May 2001 B1
6232365 Weiss et al. May 2001 B1
6241928 Hatsuda et al. Jun 2001 B1
6242504 Meyer-Roscher et al. Jun 2001 B1
6245922 Heilmann et al. Jun 2001 B1
6252016 Wu et al. Jun 2001 B1
6254965 McGuire et al. Jul 2001 B1
6262329 Brunsveld et al. Jul 2001 B1
6280822 Smith et al. Aug 2001 B1
6284360 Johnson et al. Sep 2001 B1
6287685 Janssen et al. Sep 2001 B1
6294249 Hamer et al. Sep 2001 B1
6315851 Mazurek et al. Nov 2001 B1
6316099 George et al. Nov 2001 B1
6326450 Shipston et al. Dec 2001 B1
6339111 Moon et al. Jan 2002 B1
6340719 Goeb et al. Jan 2002 B1
6348249 Meyer Feb 2002 B2
6353130 Aichinger et al. Mar 2002 B1
6372827 Johnson et al. Apr 2002 B2
6383958 Swanson et al. May 2002 B1
6399031 Herrmann et al. Jun 2002 B1
6406782 Johnson et al. Jun 2002 B2
6413629 Kimura Jul 2002 B1
6414087 Hashemzadeh et al. Jul 2002 B1
6416838 Arney et al. Jul 2002 B1
6421052 McGuire Jul 2002 B1
6436529 Deeb et al. Aug 2002 B1
6436532 Moon et al. Aug 2002 B1
6441092 Gieselman Aug 2002 B1
6444305 Banovetz et al. Sep 2002 B2
6448301 Gaddam et al. Sep 2002 B1
6448337 Gaddam et al. Sep 2002 B1
6448339 Tomita Sep 2002 B1
6455140 Whitney et al. Sep 2002 B1
6458454 Kreckel Oct 2002 B1
6469118 Su Oct 2002 B1
6475609 Whitney et al. Nov 2002 B1
6485589 Johnson et al. Nov 2002 B1
6489022 Hamilton et al. Dec 2002 B1
6492019 Shipston et al. Dec 2002 B1
6495253 Koyama et al. Dec 2002 B1
6497949 Hyde et al. Dec 2002 B1
6503621 Ma et al. Jan 2003 B1
6513897 Tokie Feb 2003 B2
6514373 Hill et al. Feb 2003 B1
6517661 Hill, IV et al. Feb 2003 B2
6517910 Wright et al. Feb 2003 B2
6518343 Lucast et al. Feb 2003 B1
6524649 Sher et al. Feb 2003 B1
6537659 Karim et al. Mar 2003 B2
6551439 Hill, IV et al. Apr 2003 B1
6566549 Greenblatt et al. May 2003 B1
6579915 Kroll et al. Jun 2003 B2
6586082 Brown Jul 2003 B1
6599602 Bennett et al. Jul 2003 B2
6602454 McGuire et al. Aug 2003 B2
6602580 Hamilton et al. Aug 2003 B1
6605738 Ho et al. Aug 2003 B1
6613411 Kollaja et al. Sep 2003 B2
6624273 Everaerts et al. Sep 2003 B1
6632907 Mizota et al. Oct 2003 B1
6635690 Heilmann et al. Oct 2003 B2
6649787 Nakahara et al. Nov 2003 B1
6652970 Everaerts et al. Nov 2003 B1
6656307 Northey Dec 2003 B2
6664306 Gaddam et al. Dec 2003 B2
6677402 Gaddam et al. Jan 2004 B2
6689853 Campbell et al. Feb 2004 B2
6740399 George et al. May 2004 B1
6759110 Fleming et al. Jul 2004 B1
6768021 Horan et al. Jul 2004 B2
6773647 McGuire et al. Aug 2004 B2
6800278 Perrault et al. Oct 2004 B1
6803072 Sher et al. Oct 2004 B2
6815035 Bennett et al. Nov 2004 B2
6818292 Hamilton et al. Nov 2004 B2
6825278 Holub et al. Nov 2004 B2
6828363 Beuermann et al. Dec 2004 B2
6838142 Yang et al. Jan 2005 B2
6841234 Lhila et al. Jan 2005 B2
6846948 Riondel et al. Jan 2005 B2
6855226 Hill, IV et al. Feb 2005 B2
6855386 Daniels et al. Feb 2005 B1
6858295 Diehl et al. Feb 2005 B2
6864322 Gehlsen et al. Mar 2005 B2
6866899 Wright Mar 2005 B2
6872342 Giachetto et al. Mar 2005 B2
6878440 Yamanaka et al. Apr 2005 B1
6881471 Toussant et al. Apr 2005 B2
6883908 Young et al. Apr 2005 B2
6893655 Flanigan et al. May 2005 B2
6903151 Lucast et al. Jun 2005 B2
6903243 Burton et al. Jun 2005 B1
6906164 DeBruin Jun 2005 B2
6911243 Sher et al. Jun 2005 B2
6926959 Kroll et al. Aug 2005 B2
6939428 Hill, IV et al. Sep 2005 B2
6982107 Hennen Jan 2006 B1
7015286 Heilmann et al. Mar 2006 B2
7015295 Takizawa et al. Mar 2006 B1
7056984 Kawabata et al. Jun 2006 B2
7074295 Bellafore et al. Jul 2006 B2
7074858 Heilmann et al. Jul 2006 B2
7087279 Callahan et al. Aug 2006 B2
7105206 Beck et al. Sep 2006 B1
7119128 Husemann et al. Oct 2006 B2
7182829 Smith et al. Feb 2007 B2
7217455 Valdez May 2007 B2
7229517 Bellafore et al. Jun 2007 B2
7244863 Yada et al. Jul 2007 B2
7250210 Mazurek et al. Jul 2007 B2
7276278 Kamiyama et al. Oct 2007 B2
7300555 Schroeder Nov 2007 B2
7332206 Callahan et al. Feb 2008 B2
7345139 DeBruin Mar 2008 B2
20010053814 Yamamoto et al. Dec 2001 A1
20020007030 Brant Jan 2002 A1
20020077509 Sugise et al. Jun 2002 A1
20030153699 Ameduri et al. Aug 2003 A1
20030199669 Saito et al. Oct 2003 A1
20040077744 Naylor et al. Apr 2004 A1
20040176561 Janeiro et al. Sep 2004 A1
20050107629 Hershberger et al. May 2005 A1
20060036047 Klostermann et al. Feb 2006 A1
20060205972 Clymo et al. Sep 2006 A1
20070112154 Lee et al. May 2007 A1
20070129512 Blitz et al. Jun 2007 A1
20070299226 Park et al. Dec 2007 A1
20100113692 McGuire et al. May 2010 A1
20100267855 McGuire, Jr. Oct 2010 A1
Foreign Referenced Citations (14)
Number Date Country
880938 Jun 1953 DE
4344358 Jul 1995 DE
10036879 Sep 2001 DE
10063510 Jul 2002 DE
0795535 Sep 1997 EP
0795536 Sep 1997 EP
0891990 Jan 1999 EP
1352400 May 1974 GB
2159826 Dec 1985 GB
2001-106654 Apr 2001 JP
2001-131116 May 2001 JP
2005-230585 Sep 2005 JP
WO-9852904 Nov 1998 WO
WO-2006020787 Feb 2006 WO
Related Publications (1)
Number Date Country
20100267855 A1 Oct 2010 US