US20200071551A1

US20200071551A1 - Low odor radiation curable ink compositions

Info

Publication number: US20200071551A1
Application number: US16/678,499
Authority: US
Inventors: Joshua Samuel; Huilei Zhang
Original assignee: Electronics for Imaging Inc
Current assignee: Electronics for Imaging Inc
Priority date: 2016-05-25
Filing date: 2019-11-08
Publication date: 2020-03-05
Also published as: WO2017205609A1; US20170342281A1; EP3464491A4; EP3464491A1; US10487226B2

Abstract

The present invention relates to low odor radiation curable ink compositions. The composition comprises 10-40% w/w of 4-hydrobutylacrylate, 5-25% of a urethane (math)acrylate oligomer, 10-55% of diacrylates, one or more photoinitiators, one or more additives, and one or more pigments. The composition excludes many monofunctional monomers that have distinct odor and are commonly used in an ink jet composition.

Description

This patent application is a continuation of U.S. application Ser. No. 15/472,630, filed on Mar. 29, 2017, which claims priority from U.S. Provisional Application No. 62/341,303, filed on May 25, 2016, each of which are incorporated herein by reference in their entirety.

TECHNICAL FIELD

This invention relates to low odor radiation curable ink compositions. In particular, the ink composition includes a polymerizable monofunctional monomer 4-hydrobutylacrylate and excludes monofunctional monomers that have distinct odors.

BACKGROUND OF THE INVENTION

Inkjet inks used for drop on demand (DOD) printing need to use low viscosity materials to yield a viscosity of up to approximately 12 cP at jetting temperatures. Monomers have low molecular weight and high vapor pressure. Many of the monomers used in the inkjet inks have distinct odors that can lead to taint when used on secondary or tertiary packaging.
Monomers may have multiple acrylate groups. The higher number of acrylate groups leads to a polymer with a higher degree of cross linking, which reduces odor. A higher degree of cross linking also leads to a faster curing material and a harder material. However, higher cross linking will lead to a more brittle ink which will not be acceptable for application that requires bending of the ink layer without cracking such as in corrugated board where creasing is required.

DETAILED DESCRIPTION OF THE INVENTION

This invention addresses the need for a fast curing, flexible, low odor ink, particularly for use in single pass printing of paper based corrugated stock such as cardboard boxes. The present invention provides an ink that has a very low odor and good flexibility. The ink is curable by actinic radiation, more specifically using LEI) generated light. The ink is designed to be suitable for packaging, particularly for single pass printing on paper-based corrugated material. The ink exhibits minimal odor in the wet state and in the fully cured state.
The present invention provides a low odor radiation curable ink composition. Low odor is defined by the response of a panel of people who are not habituated to the printed article. Low odor does not have a strong smell or an undesired smell, and is in general acceptable to people. The ink composition comprises: 10-40% w/w of 4-hydrobutylacrylate (4HBA), 5-25% of one or more urethane (meth)acrylate oligomer, 10-55% of diacrylates, one or more photoinitiators, and one or more additives. The present ink composition provides a low viscosity of about 8-14 at 45° C. which is required to be able to jet from the printer head. The present ink composition excludes monofunctional monomers that have an undesired odor such as vinyl caprolactam, 2-phenoxyethyl acrylate, isodecyl acrylate, 3,3,5-trimethylcyclohexyl acrylate, isooctyl acrylate, octyldecyl acrylate, isobornyl acrylate, cycloaliphatic acrylate monomer, benzyl acrylate, di(ethylene glycol) 2-ethylhexyl acrylate, tridecyl acrylate, 2(2-ethoxyethoxy) ethyl acrylate, lauryl acrylate, and tetrahydrofurfuryl acrylate. By exclusion, it means that the ink composition does not contain a substantial amount of the undesired monofunctional monomers. “A substantial amount”, as used herein, refers to at least 5%, preferably at least 1%, at least 0.3%, or at least 0.1%.
The present composition uses a limited number of monoactylates that have been identified as low odor, in combination with 4-HBA. These compounds have acceptably high cure rates in combination with a diacrylate at a sufficiently low level to enable a fast cure rate with sufficient flexibility and with an acceptably low odor for applications such as tertiary packaging.
The present invention is also directed to paper based corrugated stock such as a cardboard box having the fast curing, flexible, low odor ink composition printed and cured on its surface.
Unless specifically mentioned, all percentages (%) in this application refer to % by weight, unless otherwise specified.

Mono Functional Monomers

The present ink composition comprises 10-50%, by weight of one or more mono-functional monomers that have no odor and acceptable low odor. Mono-functional monomers do not crosslink with each other and provide flexibility of ink film after curing. 4-Hydroxybutyl acrylate (4HBA, CAS No.: 2478-10-6), which is a polymerizable monofunctional monomer, is an essential mono-functional monomer in the present ink composition. 4HBA has a low viscosity and has low odor; it has sufficiently high flexibility with a high cure rate. 4HBA, with a primary hydroxyl group at the end of a longer alkyl chain, gives excellent scratch resistance due to its high crosslinking ratio and unique flexibility. The present ink composition comprises 10-40% why of 4HBA, and preferably 15-30% or 15-25% 4HBA.
The present ink composition optionally includes other low-odor mono functional monomers. In one embodiment, mono-functional monomers include acrylates or methacrylates. In another embodiment, mono-functional monomers include a vinyl ether. Examples of suitable mono-functional monomers for the present ink composition include, but are not limited to, cyclic trimethylolpropane formal acrylate (SR531), Genomer 1122 (a urethane acrylate) from RAHN, ethyl vinyl ether, and mono-functional methoxylated PEG (350) acrylate (SR55 alkoxylated phenol acrylate monomer (SR9087), alkoxylated tetrahydrofurfuryl acrylate (SR611), ethoxylated (4) nonyl phenol acrylate (SR504), and ethoxylated (8) nonyl phenol acrylate (Miramer M166 from RAHN).
Monomers that have odor and are excluded from the present ink composition are shown in Table 1.

TABLE 1

Strong
Smell	Chemical Name	CAS #	Viscosity cP

VCAP	Vinyl caprolactam	2235-00-9
PHEA	2-phenoxyethyl acrylate	48145-04-6	12
IDA	Isodecyl acrylate	1330-61-6	5
TMCHA	Acrylic monomer	86178-38-3, 116-	6
	3,3,5-trimethylcyclohexyl acrylate	02-9
IOA	isooctyl acrylate	29590-42-9	5
ODA	Octyldecyl acrylate	2499-59-4, 2156-	4
		96-9
IBOA	Isobornyl acrylate	5888-33-5	8
TBCHA	Cycloaliphatic acrylate monomer	84100-23-2	9
BZA	Benzyl acrylate	2495-35-4	5
EH(EO)2A	Di(ethylene glycol) 2-ethylbexyl	117646-83-0	15
	acrylate

Smell	Chemical Name	CAS #	Viscosity

TDA	Tridecyl acrylate,	3076-04-8	7
EOEOEA	2(2-ethoxyethoxy) ethyl acrylate	7328-17-8	6
LA	Lauryl acrylate	2156-97-0	6

Smell,
volatility
and
irritation	Chemical Name	CAS #	Viscosity

THFA	Tetrahydrofurfuryl acrylate	2399-48-6	6

Other than vinyl Caprolactam, the above excluded monomers are monofunctional acrylates. Monofunctional acrylates are important components for the present ink composition because they provide sufficient flexibility of the ink. Monofunctional acrylates have only one acrylate group, and if they exhibit a strong odor, they are most prone to leaving a residual odor in the cured product because they do not crosslink completely into the film and are volatile.

Diacrylates

In addition to mono-functional monomers, the present ink composition comprises 10-55%, preferably 30-55%, of acceptable low odor or no odor di-functional monomers to speed up the polymerization process and increase the chemical resistance. Examples of suitable di-functional monomer include, but are not limited to, diacrylate or dimethacrylate of diols and potyetherdiols, such as propoxylated neopentyl glycol diacrylate, 1, 6-hexanediol diacrylate, dipropylene glycol diacrylate, tripropylene glycol diacrylate, triethylene glycol diacrylate, 1,4-butanediol diacrylate (e.g, SR213), alkoxylated aliphatic diacrylate (e.g. SR9209A), diethylene glycol diacrylate, alkoxylated hexanediols diacrylates (e.g, SR561, SR 562, SR563, SR564 from Sartomer Co., Inc), polyethylene glycol (200) diacrylate (SR259), and polyethylene glycol (400) diacrylate (SR344).
Preferred diacrylates for the present ink composition includes propoxylated neopentyl glycol diacrylate (CAS No: 84170-74-1), dipropylene glycol diacrylate (CAS No: 57472-68-I). and tripropylene glycol diacrylate (CAS No: 42978-66-5).

Urethane (Math)Acrylate Oligomer

It is preferable to use an oligomer component of low viscosity, low volatility, high reactivity, low glass transition temperature, and good adhesion to multiple substrates in the ink compositions. The functionality of the oligomer component is preferably not greater than 3, and more preferably not greater than 2. The low functionality contributes to more flexible ink compositions.
The present ink composition comprises at least 5%, preferably at least 10%, and up to 25% (for example, 10-25%) of a flexible urethane acrylate oligomer. Urethane acrylate oligomers suitable for the present ink composition include CN9009, CN990, CN991, from Sartomer, Ebercryl 8402, Ebersryl 8411 from Allnex, Genomer 4215, Genomer 4230 and Geonmer 4267 from RAHN, Miramer PU2100, Miramer PU2200 from MIWON, Photomer 6891, Photomer 6892 and Photomer 6230 from IGM, NeoRad U-61 and NeoRad U-20 from DSM.

Photoinitiators

The ink composition of the present invention comprises 1-15% by weight of one or more photoinitiators.
Acyl phosphine oxide photoinitiators include diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TPO), phenylbis(2,4,6-trimethylbenzoyl)-phosphine oxide (Irgacure 819), ethyl (2,4,6-trimethylbenzoyl)-phenylphosphine oxide (TPO-L), and their derivatives and polymeric version derivatives.
In addition to acylphpsphine oxide, the present ink composition may comprise other photoinitiators such as thioxanthones: 2-isopropyl thioxanthone, 2-chlorothioxanthone, 2-methylthioxanthone, 2-ethylthioxanthone, 2-tert-butylthioxanthone, 2-phenylthioxanthone, 2-benzylthioxanthone, 2-benzylthioxanthone, and 4-isopropytthioxanthone, polymeric thioxanthones.
Other useful photoinitiators that may be used in the present ink composition include, but are not limited to, 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)-butanone-1 (Irgacure 369), 2-methyl-1-[4-(methylthio)phenyl]-2-(4-morpholinyl)-1-propanone (Irgacure 907), 2-(4-methylbenzyl)-2-(dimethylamino)-4-morpholinobutyrophenone (Irgacure 379), 1-hydroxycyclohexylphenyl ketone, 2-hydroxy-4′-(2-hydroxyethoxy)-2-methylpropiophenone, 2-hydroxy-2-methyl-1-phenyl-1-propanone, oligo or dimer (2-hydroxy-2-methyl-1-[4-(1-methylvinyl) phenyl]propanone). Suitable blends of photoinitiators commercially available include, but are not limited to, those under the designations of Darocur 4265, Irgacure 2022, and Irgacure 2100 from BASF; and Esacure KT37, Esacure KT55, and Esacure KTO46 IGM.

Additives

The present ink composition may further include 0.01-5%, preferably 0.1-3% by weight of one or more additive components. Various additives may be included in the ink compositions, including one or more of a surfactant, a leveling additive, a stabilizer, and other suitable additives.
A surfactant is used to reduce the surface tension of the ink compositions to improve wetting property of the inks on substrates. The amount of surfactant in the ink compositions is 0.01-2% by weight, and preferably 005-1% by weight. It is preferred that the surfactant comprises at least one polysiloxane acrylate, also known as a silicone acrylate, which participates in the radiation curing process to be part of cured ink. Examples of a suitable surfactant include, but are not limited to, those under the designations of TEGORAD 2200N, TEGORAD 2100, and TEGORAD 2300 from Evonik Resource Efficiency GmbH, TEGO Products and BYK 307, BYK 330, BYK 377 and BYK 3510 (BYK CHEMIE GMBH (Wesel, FRG).
A leveling additive may be used to improve the flowing property of ink to produce a more uniform surface of ink film. The amount of leveling agent in the ink compositions is 0.1-2% by weight. Examples of suitable leveling agent include, but are not limited to, those under the designation of BYK 361N, BYK 353, and BYK 354 and so on, (BYK CHEMIE GMBH).
A stabilizer is used to improve the shelf life and photolytic stability of ink compositions. Stabilizers in the ink compositions can include an ultraviolet light stabilizer and hindered amine light stabilizer. These stabilizers are used to improve the outdoor durability and weatherability of cured ink. Commercially available ultraviolet light stabilizers include, but are not limited to, those under the designation of TINUVIN® 460, TINUVIN® 479, TINUVIN® 171, TINUVIN® 928, TINUVIN® 123, TINUVIN® 1130, TINUVIN® 400 TINUVIN® 152 and TINUVIN® 292 from BASF AG, Ludwigshafen, FRG. One or more UV inhibitor/stabilizers may be present in the ink compositions. They can be present in the ink compositions in amounts of 0.01%-2% by weight, and more specifically 0.1%-1% by weight.
A free radical scavenger stabilizer is used to improve the stability of ink against heat. Examples of a free radical scavenger include, but are not limited to, hydroquinone, 4-methoxyphenol, hindered phenol, etc. The amount of free radial scavenger stabilizer can be present in ink compositions in 0.05-2% by weight, and more specifically 0.1-0.75% by weight. A small amount is preferably used in the ink compositions to minimize their interference with the radiation curing process. Examples of free radical scavengers include, but are not limited to, hydroquinone, 4-methoxyphenol, hindered phenol such as IRGASTAB® UV 22 (an in-can stabilizer that inhibits early polymerization in UV curable ink and coating formulations) from BASF, and IN515 (tris(N-nitroso-N-phenyl-hydroxylamine)-aluminum salt+92% 2-phenoxyethyl acrylate) from IGM.

Colorant Component

The present ink composition may further comprise a colorant component if color is desired. The colorant can be pigments, dyes, or a combination of pigments and/or dyes. The amount of colorant component in the ink compositions is in the range of 0-20% by, more preferably 0-8% by weight. A clear ink has 0% colorant.
Examples of suitable Pigments include, but are not limited to, those under the designation of Pigment Blue 1, Pigment Blue 15, Pigment Blue 15:1, Pigment Blue 15:2, Pigment Blue 15:3, Pigment Blue 15:4, Pigment Blue 15:6, Pigment Blue 16, Pigment Blue 24, and Pigment Blue 60; Pigment Brown 5, Pigment Brown 23, and Pigment Brown 25; Pigment Yellow 3, Pigment Yellow 14, Pigment Yellow 16, Pigment Yellow 17, Pigment Yellow 24, Pigment Yellow 65, Pigment Yellow 73, Pigment Yellow 74, Pigment Yellow 83, Pigment Yellow 95, Pigment Yellow 97, Pigment Yellow 108, Pigment Yellow 109, Pigment Yellow 110, Pigment Yellow 113, Pigment Yellow 120, Pigment Yellow 128, Pigment Yellow 129, Pigment Yellow 138, Pigment Yellow 139, Pigment Yellow 150, Pigment Yellow 154, Pigment Yellow 156, and Pigment Yellow 175; Pigment Green 1, Pigment Green 7, Pigment Green 10, and Pigment Green 36; Pigment Orange 5, Pigment Orange 15, Pigment Orange 16, Pigment Orange 31, Pigment Orange 34, Pigment Orange 36, Pigment Orange 43, Pigment Orange 48, Pigment Orange 51, Pigment Orange 60, and Pigment Orange 61; Pigment Red 4, Pigment Red 5, Pigment Red 7, Pigment Red 9, Pigment Red 22, Pigment Red 23, Pigment Red 48, Pigment Red 48:2, Pigment Red 49, Pigment Red 112, Pigment Red 122, Pigment Red 123, Pigment Red 149, Pigment Red 166, Pigment Red 168, Pigment Red 170, Pigment Red 177, Pigment Red 179, Pigment Red 190, Pigment Red 202, Pigment. Red 206, Pigment Red 207, and Pigment Red 224; Pigment Violet 19, Pigment Violet 23, Pigment Violet 37, Pigment Violet 32, Pigment Violet 42; and Pigment Black 6 or 7 (The Colour Index, Vols. 1-8, by the Society of Dyers and Colourists, Yorkshire, England), Black PB 2 and 5; carbon black; titanium dioxide (including rutile and anatase); zinc sulfide, and the like or a mixture thereof.
If pigment is used in the ink compositions, preferably, the pigment is pre-dispersed prior to incorporation, generally into one or more of the monomer and/or oligomer components used in the ink compositions. In embodiments, the colorant is added as a pigment slurry prepared with a portion of a reactive diluent such as propoxylated 2-neopentyl glycol diacrylate (SR-9003, Sartomer USA, LLC). Dispersion agents generally are used to improve the stability of dispersion by reducing or avoiding the possibility of pigment particle settling or agglomerating. Examples of suitable dispersion agents include, but are not limited to, those under the designations of Solsperse 32000 from Lubrizol® Advanced Materials, and DisperBYK 111 and DisperBYK180 from Byk Chemi®. The pigment in the dispersion can be 20-80% by weight. Other additives such as stabilizers, flowing additive, etc. can be incorporated during the dispersion process to improve the stability of dispersion.
The invention is further illustrated by the following examples.

EXAMPLES

Example 1. A Low Odor Ink Composition

Table 1 shows the components for a low odor ink composition.

TABLE 1

Ink Composition

Function	Chemical Name	weight %

Difunctional monomer	Dipropylene glycol diacrylate	41.5
	DPGDA
Difunctional monomer	Propoxylated (2) neopentyl	8
	glycol diacrylate NPG(PO)2DA
Monofunctional	4-Hydrobutylacrylate	25
monomer
Oligomer	Aliphatic urethane diacrylate	10
Photoinitiator	TPO	5
Photoinitiator	TPO-L	5
Photoinitiator	IRGACURE ® 819	2
Additive	Polyacrylate Leveling agent	0.5
Additive	Silicone-containing	0.5
	surface additive
Pigment	Cyan pigment	2
Stabilizer	STABILIZER UV22	0.5
		100

The above ingredients (chemicals) were added to a container, and mixed by magnetic or mechanic mixers to form the cyan ink. Then the ink was filtered through 1 micron filter.
It is to be understood that the foregoing describes preferred embodiments of the present invention and that modifications may be made therein without departing from the scope of the present invention as set forth in the claims.

Claims

What is claimed is:

1. A paper-based corrugated stock having a low odor radiation curable ink composition printed and cured on its surface, wherein the ink composition comprises:

15-30% w/w of 4-hydrobutylacrylate,

30-55% w/w of diacrylate selected from the group consisting of: dipropylene glycol diacrylate, dipropylene glycol diacrylate, propoxylated neopentyl glycol diacrylate, aliphatic urethane diacrylate, and a combination thereof,

one or more photoinitiators,

one or more additives, and

one or more pigments;

wherein the ink composition contains less than 1% of monofunctional momoners that have an undesired odor selected from the group consisting of: vinyl caprolactam, 2-phenoxyethyl acrylate, isodecyl acrylate, 3,3,5-trimethylcyclohexyl acrylate, isooctyl acrylate, Octyldecyl acrylate, isobomyl acrylate, cycloaliphatic acrylate monomer, benzyl acrylate, di(ethylene glycol) 2-ethyl hexyl acrylate, tridecyl acrylate, 2(2-ethoxyethoxy) ethyl acrylate, lauryl acrylate, tetrahydrofurfuryl acrylate, and any combination thereof.

2. The paper-based corrugated stock of claim 1, comprising 0.01-5% by weight of the one or more additives.

3. The ink composition of claim 2, additive is a surfactant, a leveling additive, dispersant, or a stabilizer.

4. The ink composition of claim 1, comprising 1-8% by weight of the one more pigments.

5. The ink composition of claim 1, ink viscosity is 8-14 cP at 45° C. or less than 30 cp at 25° C.