U.S. patent application number 11/126683 was filed with the patent office on 2005-09-29 for stabilization of fluorescent dyes in vinyl articles using hindered amine light stabilizers.
This patent application is currently assigned to 3M Innovative Properties Company. Invention is credited to Coderre, James C., Lightle, Vera L., Pavelka, Lee A., White, Kenneth M..
Application Number | 20050213213 11/126683 |
Document ID | / |
Family ID | 25498098 |
Filed Date | 2005-09-29 |
United States Patent
Application |
20050213213 |
Kind Code |
A1 |
White, Kenneth M. ; et
al. |
September 29, 2005 |
Stabilization of fluorescent dyes in vinyl articles using hindered
amine light stabilizers
Abstract
A durable colored article having fluorescent properties
comprises a substantially solventless polyvinyl chloride matrix, a
thioxanthene fluorescent dye, and a secondary or tertiary hindered
amine light stabilizer having a molecular weight less than about
1000 grams/mole. The invention has the advantage in that it
provides a flexible polyvinyl chloride film that exhibits durable
fluorescent colors.
Inventors: |
White, Kenneth M.; (Oakdale,
MN) ; Pavelka, Lee A.; (Cottage Grove, MN) ;
Lightle, Vera L.; (Hudson, WI) ; Coderre, James
C.; (Lake Elmo, MN) |
Correspondence
Address: |
3M INNOVATIVE PROPERTIES COMPANY
PO BOX 33427
ST. PAUL
MN
55133-3427
US
|
Assignee: |
3M Innovative Properties
Company
|
Family ID: |
25498098 |
Appl. No.: |
11/126683 |
Filed: |
May 11, 2005 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
11126683 |
May 11, 2005 |
|
|
|
10304501 |
Nov 26, 2002 |
|
|
|
10304501 |
Nov 26, 2002 |
|
|
|
10028162 |
Dec 20, 2001 |
|
|
|
6526588 |
|
|
|
|
10028162 |
Dec 20, 2001 |
|
|
|
09593335 |
Jun 14, 2000 |
|
|
|
6406798 |
|
|
|
|
09593335 |
Jun 14, 2000 |
|
|
|
08956332 |
Oct 23, 1997 |
|
|
|
6110566 |
|
|
|
|
Current U.S.
Class: |
359/519 |
Current CPC
Class: |
B32B 27/20 20130101;
B32B 2307/42 20130101; B32B 2307/422 20130101; Y10T 428/31928
20150401; B32B 27/304 20130101; C09B 57/14 20130101; Y10T 428/24612
20150115; Y10T 428/24198 20150115; B32B 2307/416 20130101; Y10T
428/31699 20150401; B32B 2590/00 20130101; C08K 5/0008 20130101;
G02B 5/124 20130101; G02B 5/128 20130101; C09B 67/002 20130101;
Y10T 442/676 20150401; Y10T 428/25 20150115; B32B 2307/4026
20130101; B32B 27/08 20130101; Y10T 428/3192 20150401; B32B 2250/02
20130101; Y10T 428/24479 20150115; C09B 67/0097 20130101; Y10T
428/2996 20150115; B32B 2250/246 20130101; B32B 27/30 20130101;
B44F 1/04 20130101; Y10T 428/31935 20150401; B32B 3/30 20130101;
C08K 5/0008 20130101; C08L 27/06 20130101; Y10T 428/252 20150115;
B44F 1/08 20130101 |
Class at
Publication: |
359/519 |
International
Class: |
B32B 003/00 |
Claims
1. An article exhibiting durable color and fluorescent properties
comprising: (a) a polymeric matrix that contains a substantially
solventless polyvinyl chloride resin; (b) a thioxanthene
fluorescent dye; and (c) a hindered amine light stabilizer
comprising at least one secondary or tertiary amine groups and
having a molecular weight less than about 1000 grams/mole.
2. The article of claim 1, wherein the polymeric matrix further
comprises plasticized polyvinyl chloride resin.
3. The article of claim 1, wherein the article contains at most
about 2 weight percent of the thioxanthene fluorescent dye based on
the total weight of the article.
4. The article of claim 1, wherein the article contains about 0.01
to at about 1 weight percent of the thioxanthene fluorescent dye
based on the total weight of the article.
5. The article of claim 1, wherein the article contains at most
about 2 weight percent of the hindered amine light stabilizer based
on the total weight of the article.
6. The article of claim 1, wherein the article contains about 0.05
to about 1 weight percent of the hindered amine light stabilizer
based on the total weight of the article.
7. The article of claim 1, wherein the hindered amine light
stabilizer is selected from at least one of the group consisting of
bis-(2,2,6,6-tetramethyl-4-piperidinyl) sebacate,
bis-(1,2,2,6,6-pentamet-
hyl-4-piperidinyl)-2-n-butyl-2-(3,5-di-tert-butyl-4-hydroxybenzyl)malonate-
, and prpanedloic acid,
[(4-methoxyphenyl)-methylene]-bis-(1,2,2,6,6-penta-
methyl-4-piperidinyl)ester.
8. A fluorescent retroreflective article that comprises the article
of claim 1.
9. The article of claim 1, wherein the article is a film.
10. The article of claim 1, wherein the article is a
retroreflective cube film.
11. The article of claim 1 further comprising a protective
overlay.
12. A retroreflective sheeting exhibiting durable color and
fluorescent properties comprising: (a) a retroreflective base sheet
having a front surface; and (b) a body layer disposed on the frong
surface of the base sheet, the body layer comprising the article of
claim 1.
13. The sheeting of claim 12, wherein the retroreflective base
sheet is a cube corner based sheeting or a microsphere based
sheeting.
14. The sheeting of claim 12, wherein the sheeting is sufficiently
flexible to be wound about a mandrel having a diameter of 3
millimeters without cracking.
15. A method of making an article exhibiting durable color and
fluorescent properties comprising: (a) combining substantially
solventless polyvinyl chloride resin, a thioxanthene fluorescent
dye, and a hindered amine light stabilizer comprising at least one
secondary or tertiary amine groups having a molecular weight less
than 1000 grams/mole into a mixture; and (b) forming the article
from the mixture.
16. The method of claim 15, wherein the article is formed by either
extrusion or calendaring.
17. The method of claim 15, wherein the extrusion temperature or
calendaring temperature is about 175.degree. C. to about
205.degree. C.
18. The method of claim 15, wherein the article contains at most
about 2 weight percent of the thioxanthene fluorescent dye based on
the total weight of the article.
19. The method of claim 15, wherein the article contains about 0.01
to about 1 weight percent of the thioxanthene fluorescent dye based
on the total weight of the article.
20. The method of claim 15, wherein the article contains at most
about 2 weight percent of the hindered amine light stabilizer based
on the total weight of the article.
21. The method of claim 15, wherein the article contains about 0.05
to about 1 weight percent of the hindered amine light stabilizer
based on the total weight of the article.
22. The method of claim 15, wherein the article is disposed on a
front surface of a retroreflective base sheet.
23. The method of claim 22, wherein the retroreflective base sheet
is cube corner based or microsphere based.
24. A fluorescence-stabilized polymeric composition comprising: a)
polyvinyl chloride; b) a fluorescent dye; c) an ultraviolet
absorber; and d) a hindered amine light stabilizer compound.
25. A fluorescence-stabilized polymeric composition of claim 24
wherein said fluorescent dye is a thioxanthene.
26. A fluorescence-stabilized polymeric composition of claim 24
wherein said ultraviolet absorber is a benzophenone.
27. A retroreflective structure comprising the polymeric
composition of claim 24.
Description
TECHNICAL FIELD
[0001] The present invention pertains to polyvinyl chloride
articles that exhibit durable fluorescent colors through the use of
selected hindered amine light stabilizers.
BACKGROUND
[0002] Articles containing colorants lose their color when exposed
to solar radiation for extended time periods. For example, articles
placed outdoors throughout the summer often tend to display a faded
version of their original color by the time autumn arrives.
Although this fading occurs in both conventional and fluorescent
colorants, the problem is more acute with fluorescent
colorants.
[0003] The life of fluorescent colored articles is typically in the
range of months when exposed to daily solar radiation, whereas the
life of articles that use conventional colorants can be in the
range of years. Although generally less stable, fluorescent
colorants nonetheless find frequent use because of their ability to
increase an article's visibility. Unlike conventional colorants,
fluorescent colorants can take light that they absorb and reemit it
in the visible spectrum. This innate property allows fluorescent
articles to exhibit an enhanced visual contrast between the colored
article and its surrounding environment.
[0004] Investigators in the retroreflective art have attempted to
stabilize polymeric articles containing fluorescent colorants using
various means. For example, Burns et al. in U.S. Pat. No. 5,605,761
teach the use of a hindered amine light stabilizer (HALS) to
maintain the durability of articles containing fluorescent dyes in
a polycarbonate polymeric matrix. The document further discloses
that the fluorescent dye may be thioxanthene, perylene imide, or
thioindigoid dyes, and the HALS may be compounds from the
2,2,6,6-tetraalkyl piperidine class of compounds. While these
articles are extremely useful in maintaining fluorescent color
stability, they are not very flexible due to the polycarbonate
matrix's inherent rigidity.
[0005] Others, such as Pavelka et al. in U.S. Pat. No. 5,387,458
have attempted to maintain fluorescent colors by using an
ultraviolet screening layer that screens out ultraviolet (UV)
radiation in the range of 340 to 400 nanometers. The document also
discloses that the fluorescent color resides in a separate layer
rather than in the screening layer. Although these articles are
highly beneficial because of their stable fluorescent colors, they
do present the need of having two separate layers that can add cost
to the construction. Furthermore, the screening layer may not be
effective in reducing the degradation of the fluorescent dye caused
by dye absorbtion of visible radiation.
[0006] Polyvinyl chloride (PVC) films are useful in many
applications because of their flexibility and commercial
availability. UV absorbing stabilizers have been commonly used in
polyvinyl chloride articles to light stabilize the polymer matrix.
See, e.g., Marice McMurrer, Update: UV Stabilizers, PLASTICS
COMPOUNDING 40 (January/February 1985). UV stabilizers, however,
are not effective in stabilizing fluorescent dyes in the
matrix.
[0007] Although PVC films containing fluorescent dyes are widely
available today, they tend to have very poor color retention.
Factors contributing to the color fading include lack of dye
solubility in the PVC host matrix, dye migration, and minimal
protection offered by the resin against photodegradation.
[0008] Technical publications have suggested that HALS, with its
amine group in the molecular structure, may not be compatible with
PVC. For example, T. Hjertberg and E. M. Sorvik stated in Thermal
Degradation of PVC, in DEGRADATION AND STABILISATION OF PVC, E. D.
Owen (editor) 21, 69 (1984) that amines "induce dehydrochlorination
of PVC at high temperatures" leading to degradation of the PVC
matrix. In addition, HALS based on secondary or tertiary
piperidinyl amines are very basic compounds. For example,
2,2,6,6-tertamethyl piperidine has a pk.sub.b of 2.9 as compared to
4.7 for ammonia when measured in water. See Can Zhang et al.,
Hindered Amine Light Stabilizers: Effects of Acid Exposure, Volume
24 of JOURNAL OF POLYMER SCIENCE: PART C: POLYMER LETTERS 453, 453
(1986). Because of its alkalinity, HALS in the presence of a
volatile acid, such as hydrochloric acid (HCl), forms a salt.
Hydrochloric acid is produced by degradation and oxidation
reactions resulting from "light induced aging of PVC films." See
Martinez et al., Prediction of Photoageing Stability of Plasticized
PVC Films Containing UV-Stabilisers, Volume 54 of POLYMER
DEGRADATION AND STABILITY 49, 49 (1996). The presence of a basic
HALS in combination with a readily available source of HCl gives
rise to acid-base reactions that can degrade the PVC matrix.
[0009] Because of the flexible nature of PVC films and the
desirability using of fluorescent colorants in many articles, there
is a need for a durable colored article having these
combinations.
SUMMARY OF THE INVENTION
[0010] The present invention provides, for the first time, colored
articles exhibiting durable fluorescent properties in a solventless
PVC host matrix by incorporating a particular class of HALS to
stabilize a class of fluorescent dyes. Contrary to known teachings
that HALS may not be compatible with PVC, this invention includes
the discovery that new combinations of HALS and fluorescent dyes in
a PVC host matrix will exhibit superior stabilization of coloreds
fluorescent articles. Because the PVC host matrix has good
mechanical and thermal properties, the inventive article will be
useful in many applications, including, but not limited to, uses in
clothing, traffic control signs and devices (for example, roll-up
signs), backpacks, and water flotation safety devices.
[0011] In brief summary, the inventive article exhibits durable
color and fluorescent properties and comprises (a) a polymeric
matrix that contains substantially solventless polyvinyl chloride
resin; (b) a thioxanthene fluorescent dye; and (c) a hindered amine
light stabilizer comprising at least one secondary or tertiary
amine groups and having a molecular weight of less than about 1000
grams/mole. The inventive articles can be made by combining these
components into a mixture and forming an article from the
mixture.
[0012] Because processing of a substantially solventless
polyvinylchloride resin subjects the resin to high temperatures, it
was not predicted that a durable fluorescent-colored article would
result. As indicated above, amines can induce dehydrochlorination
of the polyvinyl chloride at high temperatures, which can lead to
degradation of the polyvinyl chloride matrix. Notwithstanding this
concept, the inventive article is surprisingly durable. Thus, the
combination of using substantially solventless polyvinyl chloride
and HALS provides benefits unsuggested in the art for forming
durable fluorescent-colored, PVC articles.
[0013] The present invention has the advantage in that it exhibits
durable color properties and fluorescence without the need to use
protective overlays. If desired, however, a protective overlay may
be used to further increase the durability of the inventive
article. The inventive articles retain their color and are able to
fluoresce for a longer time period than is normally expected even
when they are exposed to direct sunlight. Articles of the invention
therefore are good candidates for use with retroreflective
elements.
[0014] Another advantage of the invention is that the polymers,
dyes, and HALS may be processed in a solventless system, which not
only essentially eliminates solvent emissions into the atmosphere
but also reduces the article's manufacturing cost by totally
eliminating solvent use.
BRIEF DESCRIPTION OF THE DRAWINGS
[0015] The invention will be further explained with reference to
the drawings, wherein:
[0016] FIG. 1 is a cross-sectional view of a retroreflective
article 10 in accordance with the invention;
[0017] FIG. 2 is a cross-sectional view of another embodiment of
retroreflective article 20 in accordance with the invention;
[0018] FIG. 3 is a cross-sectional view of another embodiment of
retroreflective article 30 in accordance with the invention;
[0019] FIG. 4 is a cross-sectional view of another embodiment of
retroreflective article 50 in accordance with the invention;
and
[0020] FIG. 5 is a cross-sectional view of another embodiment of
retroreflective article 70 in accordance with the invention.
[0021] These figures are idealized, are not to scale, and are
intended to be merely illustrative and non-limiting.
DEFINITIONS
[0022] As used herein:
[0023] "colorant" means pigments or dyes or other substances used
to impart hue and chroma to an article;
[0024] "conventional colorant" means colorants that do not
significantly fluoresce when exposed to visible light and/or
ultraviolet light and do not exhibit fluorescent properties to the
unaided eye;
[0025] "cube film" means a single retroreflective film having cube
corner elements projecting from one surface thereof,
[0026] "cube corner sheeting" means a multilayer retroreflective
sheeting that contains cube corner elements;
[0027] "durable" refers to an enhanced retention of color or
fluorescence upon exposure to weathering;
[0028] "embedded lens" retroreflective base sheet comprises (a) a
monolayer of microspheres having a space layer and (b) a reflective
layer in optical association with the rear surface of the
microspheres and a binder layer in which the front surfaces of the
microspheres are embedded;
[0029] "encapsulated lens" retroreflective base sheet comprises (a)
a monolayer of microspheres having a reflective layer in
association with the rear surface of the microspheres and (b) a
cover layer disposed over the front surface of the microspheres
forming cells;
[0030] "exposed lens" retroreflective base sheet comprises a
monolayer of microspheres having a reflective layer in association
with the rear surface of microspheres that are embedded in a binder
layer;
[0031] "hindered amine light stabilizer" means an additive used to
light stabilize fluorescent dyes, the stabilizer having at least
one secondary or tertiary amine group;
[0032] "polymeric matrix" means the principal polymeric material in
which the fluorescent dye and hindered amine light stabilizer
reside;
[0033] "secondary amine group" means a group that contains nitrogen
(N) and has one hydrogen (H) atom bonded to the nitrogen atom;
[0034] "tertiary amine group" means a group that contains nitrogen
(N) and does not have a hydrogen (H) atom bonded to the nitrogen
atom;
[0035] "substantially solventless polyvinyl chloride resin" means a
polymeric polyvinyl chloride resin capable of being processed,
whether through extrusion or calendering, without the use of a
solvent;
[0036] "thioxanthene fluorescent dye" means a fluorescent dye
having a thioxanthene unit as part of its molecular structure;
[0037] "weathering" means exposing an article to either natural or
artificial environments including, for example, heat, light,
moisture, and ultraviolet radiation.
DETAILED DESCRIPTION OF THE ILLUSTRATIVE EMBODIMENTS
[0038] The present invention combines a substantially solventless
polyvinyl chloride host matrix with fluorescent dyes, and hindered
amine light stabilizers to yield durable, colored fluorescent
articles.
[0039] FIG. 1 shows a cube corner based retroreflective article 10
of the invention. Article 10 (commonly referred to as "cube film")
comprises a multitude of cube corner elements 12 and a land layer
14. Not shown in the figure are fluorescent dyes and hindered amine
light stabilizers. Light enters the cube film 10 through the front
or first major surface 15. The light then passes through the land
layer 14 and strikes the planar faces 11 of the cube corner
elements 12 and returns in the direction from which it came as
shown by arrow 18.
[0040] FIG. 2 shows a cube corner based retroreflective article 20
of the invention. Article 20 comprises a body layer 26 disposed on
a front or first major surface 25 of a cube film 21. The cube film
21 comprises a multitude of cube corner elements 22 and can
optionally include a land layer 24. In a preferred embodiment, the
body layer 26 comprises a substantially solventless polyvinyl
chloride matrix, fluorescent dyes, and hindered amine light
stabilizers (all not shown) and is the outermost layer of article
20. The land layer 24 is distinguished from the body layer 26 by
being a layer disposed immediately adjacent to the base of the cube
corner elements. If desired, the land layer 24, if present, and/or
the cube corner elements 22 can comprise a substantially
solventless polyvinyl chloride matrix, fluorescent dyes and
hindered amine light stabilizers.
[0041] FIG. 3 shows a microsphere based retroreflective article 30
of the invention. Article 30 comprises a body layer 36 disposed on
the front or first major surface 35 of an embedded lens
retroreflective base sheet 31. For an illustrative example of an
embedded lens sheet, see U.S. Pat. No. 4,505,967 (Bailey). Base
sheet 31 comprises a monolayer of microspheres 32 embedded in a
binder layer 33 with space layer 34, specular reflective layer 38
and optional adhesive layer 40. Light enters retroreflective
article 30 through its front surface 41. The light then passes
through the body layer 36 and the binder layer 33, strikes
microspheres 32, passes through space layer 34 to strike the
specular reflective layer 38, and returns in the direction from
which it came as shown by arrow 37.
[0042] The retroreflective base sheet can also be exposed lens or
encapsulated lens--see U.S. Pat. No. 5,316,838 (Crandall) and U.S.
Pat. No. 4,025,159 (McGrath) respectively for examples of such
sheeting. In a preferred embodiment, the body layer 36 comprises a
substantially solventless polyvinyl chloride matrix, fluorescent
dyes, and hindered amine light stabilizers.
[0043] Although not necessary, articles of the invention may
optionally include a protective overlay that may or may not include
ultraviolet absorbing agents. The overlay is preferably
substantially transparent to visible light and includes a means to
screen substantial portions of incident ultraviolet radiation. FIG.
4 illustrates a retroreflective embodiment 50 having a cube film
51. Body layer 56 is disposed on the front or first major surface
55 of cube film 51. Disposed on a first side 57 of body layer 56 is
an overlay 58. In a preferred embodiment, body layer 56 comprises a
substantially solventless polyvinyl chloride matrix, fluorescent
dyes, and hindered amine light stabilizers. Overlay 58 is
preferably coextensive with body layer 56 so as to provide the most
protection.
[0044] The polymeric matrix used in the present invention contains
substantially solventless polyvinyl chloride as the host matrix.
The polymeric matrix does not need to possess other polymers (e.g.,
acrylic polymers) to impart good durability and thus may consist
essentially of solventless polyvinyl chloride. Plasticizers may be
incorporated into the matrix to impart desirable physical
properties, such as flexibility. Illustrative examples of useful
plasticizers include di-2-ethylhexyl phthalate, commercially
available as DOP from Aristech Chemical Corp., and diisononyl
phthalate, commercially available as JAYFLEX DINP, from Exxon Corp.
UV absorbers such as hydroxybenzophenones can be added to stabilize
the PVC from ultraviolet light degradation. Other additives that
may be added as processing aids include fillers, heat stabilizers,
and lubricants.
[0045] Plasticized PVC is advantageous in that it has excellent
flexibility so as to be conformable to a variety of diverse
substrates ranging from fabrics to substrates with compound curves,
such as a traffic barrel. Articles of the invention have sufficient
flexibility to be wound at room temperature about a mandrel, having
a diameter of 3 millimeter without cracking. Plasticized PVC can
also be attached easily to a substrate, through adhesive means or
mechanical means. An illustrative mechanical means involves sewing
the inventive product onto a fabric substrate.
[0046] The substantially solventless PVC films may be made by
extruding or calendering PVC resins combined with fluorescent dyes
and HALS into a film or cube film having a nominal thickness of
about 0.025 millimeters (mm) (0.001 inch) to about 3.2 mm (0.125
inch), preferably about 0.076 mm (0.003 inch) to about 0.5 mm (0.02
inch). The latter range is preferable in that it is more useful for
retroreflective sheetings. Film thickness may vary with the
particular application. For example, if the application requires
high durability, typically a thicker film, on the order of about
0.75 mm (0.030 inch) may be more useful. The thickness of the PVC
film or cube film has an affect on the quantity of fluorescent dyes
and hindered amine light stabilizers that can be loaded into the
film.
[0047] The fluorescent dyes useful for this invention are dyes from
the thioxanthene classes of compounds. A single dye or a
combination of dyes may be used. Illustrative commercially
available thioxanthene fluorescent dyes useful in the present
invention include HOSTASOL.RTM. RED GG, HOSTASOL.RTM. YELLOW 3G,
DAY-GLO.RTM. D-304, and DAY-GLO.RTM. D-315.
[0048] A useful fluorescent orange dye is
14H-anthra[2,1,9-mna]thioxanthen- e-14-one, commercially available
as C.I. Solvent Orange 63 (HOSTASOL.RTM. RED GG) from Hoescht
Celanese, and having the following chemical structure: 1
[0049] A useful yellow fluorescent dye is
N-octadecyl-benzo[k,1]thioxanthe- ne-3,4-dicarboximide,
commercially available as C.I. Solvent Yellow 98 (HOSTASOL.RTM.
YELLOW 3G) from Hoescht Celanese, and having the following chemical
structure: 2
[0050] Another useful yellow fluorescent dye is DAY-GLO.RTM. D-304,
which is a thioxanthene compound, available from Day-Glo Color
Corp., Cleveland, Ohio. Another useful orange fluorescent dye is
DAY-GLO.RTM. D-315, also a thioxanthene compound available from
Day-Glo Color Corp.
[0051] Typically, up to 2 weight percent and preferably about 0.01
weight percent to about 1.0 weight percent of the dye is present in
the inventive film. The weight percent is based on the total weight
of the inventive film. Dye loadings outside this range may be used
in accordance with the invention to achieve the desired color. For
example, is the dye is added to a thicker film, a lower dye loading
can give the same visual effect. Articles having higher dye
loadings generally exhibit brighter fluorescence and deeper color
than articles with lower dye loadings of the same dye. Articles
having a high dye loading, however, may exhibit a self-quenching
phenomenon that occurs when molecules of the dye absorb the energy
emitted by neighboring dye molecules. This self-quenching can cause
an undesirable decrease in fluorescent brightness.
[0052] Articles that possess excess dye can become opaque--perhaps
because some of the excess dye may have not dissolved into the
polymeric matrix. For applications that require the inventive
articles to be light transmissive, such as applications requiring
retroreflection, persons skilled in the art should take care to
select an appropriate dye loading so that substantially all of the
dye dissolves into the polymeric matrix. For applications that do
not require light transmissivity, such as decorative applications,
the dye loading may not be as important because opacity is not a
problem.
[0053] Other dyes and pigments (whether fluorescent or
non-fluorescent) may be added to the present invention to adjust
the color and appearance of the article. Care should be taken,
however, to select dyes and pigments, as well as their loadings, so
as not to significantly interfere with the performance of the
fluorescent dyes in the article. If retroreflective elements are
included in the inventive article, the dyes or pigments should not
undesirably impair the article's transparency. If the inventive
article has reduced transparency, its retroreflective performance
may also be undesirably reduced.
[0054] As discussed, numerous technical articles have indicated
that a hindered amine light stabilizer (HALS), with its amine
group, is not compatible with polyvinyl chlorides. Thus the use of
certain HALS to light stabilize the inventive fluorescent colored
PVC articles is very surprising.
[0055] Without intending to be bound by theory, it is believed that
the combination of selected HALS, the substantially solventless
polyvinyl chloride host matrix, and selected fluorescent dyes in
the present invention prevents an as yet undefined degradation
and/or reaction between the dye and the polyvinyl chloride which
could otherwise occur. Insofar as we know, the advantages of the
present invention are attained through the combination of the
substantially solventless polyvinyl chloride matrix, the
thioxanthene fluorescent dye, and the hindered amine light
stabilizers described herein.
[0056] Typically, up to about 2 weight percent, and preferably
about 0.05 to about 1.0 weight percent of the HALS is contained in
the inventive article. The weight percent of HALS used is based on
the total weight of the inventive film.
[0057] Illustrative commercially available HALS useful in the
present invention include TINUVIN.RTM. 770, TINUVIN.RTM. 144, and
SANDUVOR.RTM. PR-31.
[0058] A HALS, having the chemical formula of
Bis-(2,2,6,6-tetramethyl-4-p- iperidinyl) sebacate and a molecular
weight of about 480 grams/mole, contains secondary amines, is
commercially available as TINUVIN.RTM. 770 from Ciba-Geigy Corp.,
and has the following chemical structure: 3
[0059] This HALS possesses two secondary amine groups, where the
nitrogen atom is bonded to two carbon atoms and a hydrogen
atom.
[0060] A HALS, having the chemical formula of
Bis-(1,2,2,6,6-pentamethyl-4-
-piperidinyl)-2-n-butyl-2-(3,5-di-tert-butyl-4-hydroxybenzyl)malonate
and a molecular weight of about 685 grams/mole, contains tertiary
amines, is commercially available as TINUVIN.RTM. 144 from
Ciba-Geigy Corp., and has the following chemical structure: 4
[0061] A HALS, having a chemical formula of propanedioic acid,
[(4-methoxyphenyl)-methylene]-bis-(1,2,2,6,6-pentamethyl-4-piperidinyl)es-
ter, and a molecular weight of about 529 grams/mole, contains
tertiary amines, is commercially available as SANDUVOR.RTM. PR-31
from Clariant Corp., and has the following chemical structure:
5
[0062] TINUVIN.RTM. 144 and SANDUVOR.RTM. PR-31 each possesses two
tertiary amine groups, where the nitrogen atom is bonded to three
carbon atoms.
[0063] Method of Making
[0064] The inventive film can be made using an extrusion or a
calendering method. Although both methods are useful in producing a
substantially flat film, they do so by different processes.
Extrusion involves processing a viscous melt under pressure to
force it through a shaping die in a continuous stream to form a
film. Calendering takes a mass of fused, viscous material and feeds
it between successive pairs of co-rotating, parallel rolls to form
a film. Extrusion has the advantage in that if a cube film is
desired, the feed stock leaving the extruder can be nipped directly
into a mold having cube corner recesses. Calendering, on the other
hand, has the advantage in that flexible PVC films can be
economically produced using this process.
[0065] A method of making an article exhibiting durable color and
fluorescent properties can comprise: (a) combining substantially
solventless polyvinyl chloride resin, a thioxanthene fluorescent
dye, and a hindered amine light stabilizer comprising at least one
secondary or tertiary amine groups having a molecular weight less
than 1000 grams/mole into a mixture; and (b) forming the article
from the mixture.
[0066] Typically, in an extrusion process the polymeric
resin/dye/HALS mixture is first tumble mixed together. The
polymeric resin is typically in the form of small granules. The
mixture is fed into an extruder where, with the presence of heat
and rotational action of the screw, the mixture is mixed and
changes into a viscous melt. Typically, an extruder with multiple
zones of heating is used. The extrusion temperature should be
chosen to melt the components but not be so high so as to degrade
them. Suitable extrusion temperatures, when using the fluorescent
dyes and HALS described above, range from about 175.degree. C. to
about 205.degree. C. Typically, the melt leaving the extrusion dye
is allowed to contact a chrome roll or polished casting roll to
form a substantially flat film.
[0067] If desired, the melt leaving the extrusion die is allowed to
contact a mold or tool having cube corner recesses therein. When
the melt is nipped into the mold, a cube corner film is formed
having, preferably, a minimal land layer and a multitude of cube
corner elements whose base plane is adjacent to the land layer.
See, for example, U.S. Pat. No. 5,450,235 (Smith et al.) and
International Publication No. WO 95/11464 (Benson et al.) for
descriptions of methods of producing a cube corner sheeting.
Extrusion is the preferred method for making an inventive cube
film.
[0068] The cube corner elements may optionally be vapor coated with
a metallic layer, such as vapor deposited aluminum or silver, to
increase retroreflective performance. Vapor coating the cube corner
elements, however, may cause the fluorescent cube film to have a
gray appearance, which may be undesirable for some
applications.
[0069] In a calendering process, the polyvinyl chloride resin
(typically in powder form), the fluorescent dye, and the hindered
amine light stabilizer are added to mixing unit for intensive
mixing. Other additives, such as plasticizers, UV absorbers, heat
stabilizers, fillers, and lubricants may be added for desired
physical properties and/or as processing aids. Typically the mixing
unit has a ribbon type blade and can be jacketed for heating and
cooling. During mixing, the PVC powder absorbs the additives,
including the dye and HALS, to form a powder mix. After intensive
mixing, the powder is typically cooled and fed through a screen to
remove metals because the metal particles, if present, can damage
the calender roll surface. The screened powder mixture is typically
fed into a fluxing unit for continuous mixing causing the mixture
to become a fused, viscous mass that is feed stock to be delivered
to the calender rolls. The calender rolls, typically in a four roll
setup, can be heated. In making the inventive article, the calender
rolls are heated so that their surface temperature ranges from
about 170.degree. C. to about 180.degree. C. (340 to 355.degree.
F.). Configuration of the rolls can also be an important factor.
The viscous, fused feedstock is fed to the calender where the film
or sheet is formed with the film thickness controlled by the gap
between the final rolls.
[0070] Although this sequence is typical for a calendering process,
many variations are possible depending on the end product desired.
Calendering is a preferred method for making the inventive film
because of economic efficiencies.
[0071] Given what is known in the art about amines inducing
dehydrochlorination of PVC at high temperatures, the invention
nonetheless discovered that PVC articles produced from calendering
or extrusion with temperatures as high as 205.degree. (355.degree.
F.) are durable, as shown herein by the examples.
[0072] Substantially flat films, whether produced by extrusion or
calendering, can be laminated to a preexisting retroreflective base
sheet, such as cube corner based or microsphere based sheets.
Typically, the film is laminated to the front or first major
surface of retroreflective base sheets to produce a new
retroreflective article in accordance with the present invention.
For example, as shown in FIG. 2, the body layer 26, typically a
substantially flat film, is laminated to a front or first major
surface 25 of cube film 21 to produce a retroreflective article 20
of the invention. Similarly, in FIG. 3, the body layer 36,
typically a substantially flat film, is laminated to a front or
first major surface 35 of microsphere based retroreflective base
sheet 31 to produce a retroreflective article 30 of the
invention.
[0073] In a preferred embodiment, the inventive films are used as a
carrier for radiation cured cube corner elements. These cube corner
elements comprise reactive resins capable of being crosslinked by a
free radical polymerization mechanism by exposure to actinic
radiation, for example, electron beam, ultraviolet light, or
visible light. See U.S. Pat. No. 5,450,235 (Smith et al.) and
International Publication No. WO 95/11464 for examples of such
reactive resins. The reactive resin is preferably cured in situ on
the inventive film. FIG. 5 shows a cube corner based
retroreflective article 70 of the invention manufactured in
accordance with the principles of the invention disclosed in
International Publication No. WO 95/11464 published Apr. 27, 1995,
entitled "Ultra-Flexible Retroreflective Cube Corner Composite
Sheetings and Methods of Manufacture." The embodiment in FIG. 5 is
designed to be a highly flexible retroreflective sheeting suitable
for conforming to corrugated and/or flexible surfaces.
[0074] As shown in FIG. 5, retroreflective article 70 comprises a
multitude of substantially independent cube corner elements 72 and
a body layer 76 having two major surfaces 71 and 73, the cube
corner elements projecting from the first major surface 73 and have
zero to minimal land. Thus, this embodiment has essentially no land
layer and the front surface 75 of the cube corner elements is
juxtaposed against surface 73. In a preferred embodiment, body
layer 76 comprises substantially solventless polyvinyl chloride
matrix, fluorescent dyes and hindered amine light stabilizers (all
not shown) and is the outermost layer of article 70.
EXAMPLES
[0075] The following examples are provided to illustrate different
embodiments and details of the invention. Although the examples
serve this purpose, the particular ingredients and amounts used as
well as other conditions and details are not to be construed in a
manner that would unduly limit the scope of this invention. Unless
otherwise specified, all percentages are in weight percent.
[0076] Accelerated Weathering
[0077] To simulate outdoor exposure to sunlight on an accelerated
basis, some samples were exposed to accelerated weathering in
accordance with a cycle defined by ASTM G-26 Type B, Method A. The
light source was a 6500-watt, water-cooled xenon arc device that
has borosilicate inner and outer filters. The light source exhibits
an irradiance of about 0.55 watts/meter.sup.2. The weathering cycle
consisted of 102 minutes of light at a Black Panel temperature (as
defined in the test method) of about 63.degree. C., followed by 18
minutes of exposure while subjecting the sample to deionized water
spray.
[0078] Ultraviolet-Visible (UV-Vis) Absorption Spectroscopy
[0079] The amount of fluorescent dye retained in a sample was
determined by measuring the major dye absorption band (456
nanometers (nm)) using UV-Vis spectroscopy before and after the
sample was subjected to weathering. An illustrative UV-Vis
spectrophotometer used was a Shimadzu model UV 2101-PC.
[0080] Following Beer's Law, a decrease in absorbance is related to
a reduction in dye concentration. A "percent dye retention" value
was calculated as the ratio of the peak absorbance in the weathered
sample to the peak absorbance of the original unweathered
sample.
[0081] The following abbreviations are used in the examples:
1 Abbreviations Meaning PVC Polyvinyl chloride host matrix T-770
Hindered amine light stabilizer TINUVIN .RTM. 770
Bis-(2,2,6,6-tetramethyl-4-piperidinyl) sebacate Molecular weight
of about 480 grams/mole Available from Ciba-Geigy Corp., Hawthorne,
NY. T-144 Hindered amine light stabilizer TINUVIN .RTM. 144
Bis-(1,2,2,6,6-pentamethyl-4-piperid- inyl)-2-n-butyl-2-
(3,5-di-tert-butyl-4-hydroxybenzyl)malonate Molecular weight of
about 685 grams/mole Available from Ciba-Geigy Corp. PR-31 Hindered
amine light stabilizer Propanedioic acid,
[(4-methoxyphenyl)-methylene]-
bis-(1,2,2,6,6-pentamethyl-4-piperidinyl)ester Molecular weight of
about 529 grams/mole Available from Clariant Corp., Charlotte, NC.
T-622 Hindered amine light stabilizer TINUVIN .RTM. 622 Dimethyl
succinate polymer with 4-hydroxy- 2,2,6,6-tetramethyl-1-piperidine
ethanol Molecular weight (M.sub.n) approximately greater than 2,500
grams/mole Available from Ciba-Geigy Corp. C-944 Hindered amine
light stabilizer CHIMASORB .RTM. 944FL Poly
[6-[(1,1,3,3-tetramethylbut- yl)amino]-s-triazine-2,4-
diyl][2,2,6,6-tetramethyl-4-piperidyl)im- ino]hexa-
methylene[(2,2,6,6-tetramehtyl-4-piperidyl)imino)] Molecular weight
(M.sub.n) approximately greater than 2,500 grams/mole Available
from Ciba-Geigy Corp. T-440 Hindered amine light stabilizer TINUVIN
.RTM. 440 Low molecular weight acetylated hindered amine Molecular
weight of about 435 grams/mole Available from Ciba-Geigy Corp.
C-3346 Hindered amine light stabilizer CYASORB .RTM. 3346
Oligomeric hindered amine Molecular weight (M.sub.n) approximately
greater than 1,600 grams/mole Available from American Cyanamid
Corp. SO63 Thioxanthene orange fluorescent dye HOSTASOL .RTM. RED
GG; 14H-anthra[2,1,9-mna]thioxanthene-14-one; Available from
Hoechst Celanese, Charlotte, NC. SY98 Thioxanthene yellow
fluorescent dye HOSTASOL .RTM. YELLOW 3G
N-Octadecyl-benzo[k,1]thioxanthe- ne-3,4-dicarboximide Available
from Hoechst Celanese. D-304 Thioxanthene yellow fluorescent dye
DAY-GLO .RTM. 304 Available from Day-Glo Color Corp., Cleveland,
OH. D-315 Thioxanthene orange fluorescent dye DAY-GLO .RTM. 315
Available from Day-Glo Color Corp. D-838 Coumarin fluorescent
POTOMAC YELLOW .TM. D-838 dye Available from Day-Glo Color Corp.
RED FB Anthrapyridone fluorescent red dye FLUORESCENT RED FB .TM.
Available from Keystone Aniline Corp., Chicago, IL. RED 5B
Thioindigoid fluorescent red dye HOSTASOL .RTM. RED 5B C.I. (color
index) Vat Red 41 Available from Hoechst Celanese.
Example 1
[0082] A polyvinyl chloride film having a thickness of about 0.089
mm (0.0035 inch) to about 0.11 mm (0.0045 inch) was made as
follows. PVC resin (formulation S00354 containing UV absorbers from
Alpha Chemical and Plastics Corp.) was mixed with about 0.2% SO63
fluorescent dye and about 0.5% of the T-770 HALS. The
resin/dye/HALS mixture was tumbled mixed. It was then extruded into
a substantially flat film using a single screw extruder with 5
heating zones set at about 175, 205, 205, 175 and 175.degree. C.
and the film die set at about 180.degree. C. The extruder was a
three-quarters (3/4) inch single screw Brabender extruder with
polished chrome rolls.
[0083] The sample was subjected to 100 hours of weathering, and the
data are reported in Tables 1 and 2.
[0084] Examples 2 and 3, and Comparative Examples A to E are all
made according to Example 1 with different HALS used or no HALS
used as described in Table 1. The samples were subjected to 100
hours of accelerated weathering, and the data are reported in Table
1.
2TABLE 1 EXTRUDED PVC FILMS CONTAINING SO63 FLUORESCENT DYE WITH
VARIOUS HALS Percent Dye Retention After 100 hours Example No. HALS
weathering 1 T-770 55 2 T-144 66 3 PR-31 61 Comparative A T-622 9
Comparative B C-944 14 Comparative C T-440 11 Comparative D C-3346
15 Comparative E None 7
[0085] As can be seen from the results of TABLE 1, a sample without
any HALS (Comparative E) performed worst in that nearly all of the
dye was depleted from the film. HALS that had a molecular weight
exceeding 1000 grams/mole (Comparative A, B and D) did poorly in
the stabilization of the fluorescent dye. Comparative C, having a
molecular weight of 435 grams/mole, did not perform well because it
did not contain at least one secondary or tertiary amine group.
[0086] Examples 4 to 6 were made according to Example 1 except that
different fluorescent dyes were used as shown in Table 2. Unless
otherwise specified, the samples were subjected to 100 hours of
accelerated weathering, and the data are reported in Table 2.
[0087] Comparative Examples E to N were made according to Example 1
but different fluorescent dyes were used with and without HALS as
shown in Table 2. Unless otherwise specified, the samples were
subjected to 100 hours of accelerated weathering, and the data are
reported in Table 2.
3TABLE 2 EXTRUDED PVC FILMS CONTAINING VARIOUS FLUORESCENT DYES
WITH AND WITHOUT HALS Fluorescent HALS Percent Dye Example No. Dye
Used Retention 1 SO63 T-770 55 4.sup.a SY98 T-770 56 5 D-304 T-770
53 6.sup.a D-315 T-770 39 Comparative E SO63 None 7 Comparative
F.sup.a SY98 None 37 Comparative G D-304 None 35 Comparative
H.sup.a D-315 None 17 Comparative I D-838 T-770 9 Comparative J RED
FB T-770 13 Comparative K.sup.b RED 5B T-770 5 Comparative L D-838
None 18 Comparative M RED FB None 25 Comparative N.sup.b RED 5B
None 3 .sup.aSample was subjected to 200 hours of accelerated
weathering. .sup.bSample was subjected to 50 hours of accelerated
weathering.
[0088] As shown in Table 2, samples of the invention containing
thioxanthene fluorescent dyes with T-770 HALS (Examples 1, 4, 5 and
6) outperformed those samples that did not contain thioxanthene
fluorescent dyes stabilized with the same T-770 HALS (Comparatives
I, J and K). Those samples that did contain thioxanthene
fluorescent dyes but no HALS (Comparatives E, F, G and H) did not
retain the dye as well as those that did contain HALS (Examples 1,
4, 5 and 6). Finally, comparing Comparatives I, J and K with
Comparatives L, M and N shows that non-thioxanthene fluorescent dye
samples do not retain their color even if HALS was used. Thus, in
this situation, use of HALS, even if it is the preferred HALS, was
ineffective.
Example 7
[0089] A polyvinyl chloride film was made using a pilot scale
calendering process as follows. A powder of PVC was mixed with
about 0.2% SY98 fluorescent dye and about 0.5% T-770 HALS. Other
additives, for example UV absorbers, heat stabilizers,
plasticizers, lubricants, and fillers were added either for
processing aid or to help make a flexible PVC film. The mixture was
fed through a strainer to remove metal, if present. The mixture was
continuously mixed to form a fused mass, milled, and fed through
rolls, all heated at about 177.degree. C. (350.degree. F.), to form
the inventive film about 0.13 mm to about 0.15 mm (0.005 to 0.006
inch) thick. The sample was subjected to 400 hours of accelerated
weathering and the data are reported in Table 3 below.
[0090] Comparative O
[0091] A calendered PVC film was made according to Example 7 except
that no HALS was added to the PVC powder. The sample was subjected
to 400 hours of accelerated weathering, and the data are reported
in Table 3.
4TABLE 3 CALENDERED PVC FILMS CONTAINING SY98 FLUORESCENT DYE
Percent Dye Fluorescent Retention Example No. HALS Dye (After 400
hours) 7 T-770 SY98 76 Comparative O None SY98 1.3
[0092] As shown in Table 3, calendered PVC film of the invention
containing a fluorescent dye and a HALS clearly outperformed a
sample that did not contain a HALS.
[0093] Example 4 and its comparative counterpart, Comparative E,
were both exposed to 400 hours of accelerated weathering, and the
data are reported in Table 4.
5TABLE 4 EXTRUDED PVC FILMS CONTAINING SY98 FLUORESCENT DYE
Fluorescent Percent Dye Retention Example No. HALS Dye (After 400
hours) 4 T-770 SY98 29 Comparative E None SY98 9
[0094] As shown in Table 4, extruded PVC film of the invention
containing a fluorescent dye and a HALS outperformed a sample that
did not contain a HALS.
[0095] All references cited herein are incorporated by reference in
each reference's entirety.
* * * * *