WO2020162873A1 - Impression sur textile - Google Patents

Impression sur textile Download PDF

Info

Publication number
WO2020162873A1
WO2020162873A1 PCT/US2019/016487 US2019016487W WO2020162873A1 WO 2020162873 A1 WO2020162873 A1 WO 2020162873A1 US 2019016487 W US2019016487 W US 2019016487W WO 2020162873 A1 WO2020162873 A1 WO 2020162873A1
Authority
WO
WIPO (PCT)
Prior art keywords
grams
acrylic
copolymer
shell
textile printing
Prior art date
Application number
PCT/US2019/016487
Other languages
English (en)
Inventor
Zhang-Lin Zhou
Jeffrey Matthew STUBBS
Qianhan YANG
Original Assignee
Hewlett-Packard Development Company, L.P.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hewlett-Packard Development Company, L.P. filed Critical Hewlett-Packard Development Company, L.P.
Priority to US17/416,412 priority Critical patent/US20220074134A1/en
Priority to PCT/US2019/016487 priority patent/WO2020162873A1/fr
Publication of WO2020162873A1 publication Critical patent/WO2020162873A1/fr

Links

Classifications

    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
    • D06P5/30—Ink jet printing
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
    • D06P1/5207—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • D06P1/525—Polymers of unsaturated carboxylic acids or functional derivatives thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
    • D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
    • D06P1/5207—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • D06P1/525—Polymers of unsaturated carboxylic acids or functional derivatives thereof
    • D06P1/5257—(Meth)acrylic acid

Definitions

  • Inkjet printing has become a popular way of recording images on various media. Some of the reasons include low printer noise, variable content recording, capability of high speed recording, and multi-color recording. These advantages can be obtained at a relatively low price to consumers. As the popularity of inkjet printing increases, the types of use also increase providing demand for new ink compositions.
  • textile printing can have various applications including the creation of signs, banners, artwork, apparel, wall coverings, window coverings, upholstery, pillows, blankets, flags, tote bags, clothing, etc. However, the permanence of printed ink on textiles can be an issue.
  • FIG. 1A schematically depicts an example textile printing system including an ink composition and a fabric substrate in accordance with the present disclosure
  • FIG. 1 B schematically depicts an example textile printing system including an ink composition, a fabric substrate, an inkjet printhead, and a heat curing device in accordance with the present disclosure
  • FIG. 2 provides a flow diagram for an example method of textile printing in accordance with the present disclosure.
  • FIG. 3 is a TOE curve graph showing Turn On Energy comparisons of six (6) different example ink compositions with 6 different example acrylic latex particles in accordance with the present disclosure.
  • a textile printing material set includes a fabric substrate, and an aqueous ink composition.
  • the aqueous ink composition includes an aqueous ink vehicle, pigment, and from 2 wt% to 15 wt% of acrylic core-shell latex particles having an acrylic core copolymer with a glass transition temperature from -50 °C to 30 °C and an acrylic shell copolymer having a glass transition temperature from 50 °C to 130 °C, wherein the acrylic core copolymer and the acrylic shell copolymer of the acrylic core-shell latex particles have an average weight ratio from 1 :1 to 9:1.
  • the glass transition temperature of the acrylic core copolymer can be from -25 °C to 15 °C and the glass transition temperature of the acrylic shell copolymer can be from 75 °C to 105 °C.
  • the acrylic shell copolymer can include from 30 wt% to 80 wt% copolymerized methyl
  • the acrylic shell copolymer can include from 1 wt% to 14 wt% copolymerized acrylic acid, methacrylic acid, or a combination thereof.
  • the acrylic core copolymer and the acrylic shell copolymer can independently both include copolymerized a propyl acrylate, a butyl acrylate, or a combination thereof.
  • the acrylic core copolymer and the acrylic shell copolymer can both include copolymerized n-butyl acrylate.
  • the fabric substrate can be selected from cotton, polyester, nylon, silk, or a blend thereof, for example.
  • a textile printing system includes a fabric substrate, an inkjet printhead in fluid communication with a reservoir containing an aqueous ink composition, and a heating source positioned to heat the aqueous ink composition after application onto the fabric substrate.
  • the aqueous ink composition includes an aqueous ink vehicle, pigment, and from 2 wt% to 15 wt% of acrylic core-shell latex particles having an acrylic core copolymer with a glass transition temperature from -50 °C to 30 °C and an acrylic shell copolymer having a glass transition temperature from 50 °C to 130 °C.
  • the acrylic core copolymer and the acrylic shell copolymer of the acrylic core shell latex particles in this example have an average weight ratio from 1 :1 to 9: 1.
  • the acrylic shell copolymer includes from 30 wt% to 80 wt% copolymerized methyl methacrylate, ethyl methacrylate, or a combination thereof, and/or the acrylic shell copolymer also includes from 1 wt% to 14 wt% copolymerized acrylic acid, methacrylic acid, or a combination thereof.
  • the acrylic core copolymer and the acrylic shell copolymer both include copolymerized n-butyl acrylate.
  • the heating source can be positioned and powerable to generate heat at the fabric substrate at a temperature ranging from above the glass transition temperature of the acrylic shell copolymer to 200 °C.
  • the fabric substrate can be selected from cotton, polyester, nylon, silk, or a blend thereof.
  • a method of textile printing includes jetting an aqueous ink composition onto a fabric substrate.
  • the aqueous ink composition includes an aqueous ink vehicle, pigment, and from 2 wt% to 15 wt% of acrylic core-shell latex particles having an acrylic core copolymer with a glass transition temperature from -50 °C to 30 °C and an acrylic shell copolymer having a glass transition temperature from 50 °C to 130 °C.
  • the acrylic core copolymer and the acrylic shell copolymer of the acrylic core-shell latex particles in this example have an average weight ratio from 1 :1 to 9:1.
  • the method can further include heating the fabric substrate with the aqueous ink composition thereon to a temperature ranging from above the glass transition
  • the fabric substrate can be selected from cotton, polyester, nylon, silk, or a blend thereof.
  • an example textile printing system 100 which includes a fabric substrate 110 and an ink composition 130.
  • the ink composition can be printed from an inkjet pen 120 which includes an ejector 122 or printhead, such as a thermal inkjet ejector, for example.
  • the ink composition includes water and organic co-solvent (sometimes referred to collectively as an ink vehicle), and a pigment (dispersed with a dispersant associated with a surface of the pigment).
  • the ink composition also includes acrylic core-shell latex particles.
  • the dispersant can be associated with the pigment by adsorption, ionic attraction, or by covalent attachment thereto.
  • the acrylic core-shell latex particles can have an acrylic core copolymer with a glass transition temperature from -50 °C to 30 °C and an acrylic shell copolymer having a glass transition
  • the acrylic core copolymer and the acrylic shell copolymer of the acrylic core-shell latex particles have an average weight ratio from 1 :1 to 9:1.
  • an example textile printing system 105 that includes a fabric substrate 110, an ink composition 130, an inkjet pen 120 which includes an ejector 122, e.g., inkjet printhead, and a heat curing device 140 which emits heat 150 therefrom.
  • the ink composition includes the acrylic core-shell latex particles described herein.
  • the acrylic core-shell latex particles can be formed by emulsion polymerization of selected components.
  • the emulsion polymerization can thus be conducted in accordance with conventional polymerization techniques, for example in a batch, feed, or semi-batch process.
  • a combination of first phase of monomers and second phase of monomers can be employed in combination with a charge stabilizing agent, an emulsifier, and/or an initiator, for example.
  • the first phase of monomers can be a batch or feed of softer monomers, e.g., monomers having a lower glass transition temperature (Tg), though higher Tg monomers can be used in smaller amounts, provided the resultant core copolymer results in a core latex polymer that has a Tg from -50 °C to 30 °C.
  • the acrylic core copolymer can have a Tg from -25 °C to 15 °C.
  • the second phase of monomers can be selected from harder monomers, e.g., monomers having a relatively higher glass transition temperature (Tg), though lower Tg monomers can likewise be used in smaller amounts, provided the resultant shell copolymer results in a shell latex polymer that has a Tg from 50 °C to 130 °C.
  • Tg glass transition temperature
  • the glass transition temperature of the acrylic shell copolymer is from 75 °C to 105 °C.
  • glass transition temperature (Tg) of an acrylic polymer can refer to the calculated glass transition temperature based on known Tg values for homopolymers prepared from the monomers used to form the copolymer core or the copolymer shell.
  • Monomers used to prepare the acrylic core/shell latex particles can include, for either the core or the shell (at appropriate concentrations to arrive at the glass transition temperatures described herein), various monomers, but both the core and the shell include a polymerized (meth)acrylic monomer.
  • the term“acrylic core shell latex” refers to latexes where both the core and the shell include a polymerized (meth)acrylic monomer, which is typically a copolymerized core and a copolymerized shell.
  • (meth)acrylic refers to monomers, copolymerized monomers, etc., that can either be acrylate or methacrylate (or a combination of both), or acrylic acid or methacrylic acid (or a combination of both), as the acid or salt/ester form can be a function of pH. Furthermore, even if the monomer used to form the polymer was in the form of a (meth)acrylic acid during preparation, pH modifications during preparation or subsequently when added to an ink composition can impact the nature of the moiety as well (acid form vs. salt or ester form). Thus, a monomer or a moiety of a polymer described as (meth)acrylic should not be read so rigidly as to not consider relative pH levels, ester chemistry, and other general organic chemistry concepts.
  • Examples of monomers that can be used include monoacrylates, diacrylates, or polyfunctional alkoxylated or polyalkoxylated acrylic monomers
  • Suitable monoacrylates include, for example, methyl acrylate, methyl methacrylate, solketal acrylate, methacrylic acid, acrylic acid, 6- (acrylamido)hexanoic acid, acrylamide, N-isopropyl acrylamide, dimethyl acrylamide, methacrylamide, styrene, 4-vinyl pyridine, 4-vinyl benzylchloride, N-acrylomorpholine, tert-butyl methacrylate, 6-azidohexyl methacrylate, cyclohexyl acrylate, 2-ethoxy ethyl acrylate, 2-methoxy ethyl acrylate, 2(2-ethoxyethoxy)ethyl acrylate, stearyl acrylate, tetrahydrofurfuryl acrylate, octyl acrylate, lauryl acrylate, behenyl acrylate,
  • Suitable polyfunctional alkoxylated or polyalkoxylated acrylates are, for example, alkoxylated, ethoxylated, or propoxylated, variants of the following: neopentyl glycol diacrylates, butanediol diacrylates, butanediol dimethacrylates, e.g., 1 ,3-butanediol dimethacrylate (BDDMA), trimethylolpropane triacrylates, glyceryl triacrylates, 1 ,3- butylene glycol diacrylate, 1 ,4-butanediol diacrylate, diethylene glycol diacrylate, 1 ,6- hexanediol diacrylate, tetraethylene glycol diacrylate, triethylene glycol diacrylate, tripropylene glycol diacrylate, polybutanediol diacrylate, polyethylene glycol diacrylate, propoxylated neopentyl glycol diacryl
  • the monomer can be, for example, propoxylated neopentyl glycol diacrylate, such as, for example, SR-9003 (Sartomer Co., Inc., Exton, Pa.). Suitable reactive monomers are likewise commercially available from, for example, Sartomer Co., Inc., Henkel Corp., Radcure Specialties, and the like.
  • the reaction medium used for preparing the acrylic core-shell latex particles can use both a charge stabilizing agent and an emulsifier in order to obtain a target particle size.
  • the acrylic core-shell latex particles can have a D50 particle size from about 100 nm to about 350 nm, from about 150 nm to about 350 nm, from about 200 nm to about 300 nm, or from about 240 nm to about 280 nm, for example.“D50” particle size is defined here as the particle size at which about half of the particles are larger than the D50 particle size and about half of the other particles are smaller than the D50 particle size (by weight based on the metal particle content of the particulate build material).
  • particle size with respect to the acrylic core-shell latex particles can be based on volume of the particle size normalized to a spherical shape for a theoretical diameter measurement, for example.
  • Particle size can be collected using a Malvern Zetasizer, for example.
  • the“D95” is defined as the particle size at which about 5 wt% of the particles are larger than the D95 particle size and about 95 wt% of the remaining particles are smaller than the D95 particle size.
  • Particle size information can also be determined and/or verified using a scanning electron microscope (SEM).
  • the charge stabilizing agent can be a monomer that includes acid groups suitable for stabilizing the particles in the liquid medium of the ink compositions.
  • Various charge stabilizing agents that can be used include methacrylic acid, acrylic acid, and/or a salt thereof.
  • methacrylic acid and acrylic acid are both also listed as monomers herein, but can have the dual function of copolymerization and charge stabilization.
  • Sodium salts of methacrylic acid and/or acrylic acid can be used in some specific examples.
  • the charge stabilizing agent may be employed in relatively small
  • concentrations e.g., about 0.1 wt% to about 5 wt% (based on the weight of the emulsion polymerization components).
  • the emulsifier can contribute to achieving a target particle size, but can also contribute to a desired surface tension of the acrylic core-shell latex particles, e.g., from about 35 dynes/cm to about 65 dynes/cm, from about 40 dynes/cm to about 60 dynes/cm, or about 45 dynes/cm to about 55 dynes/cm.
  • the emulsifier can include a fatty acid ether sulfate, such as lauryl ether sulfate.
  • the emulsifier may be included at relatively small concentrations, e.g., about 0.1 wt% to about 5 wt% (based on the weight of the emulsion polymerization components).
  • the emulsion polymerization is conducted in accordance with polymerization processes, such as, for example, a semi-batch process.
  • the acrylic core-shell latex particles can be synthesized by free radical initiated polymerization using a free radical initiator, for example.
  • the initiator can include a“per” compound such as a diazo compound, persulfate, per-oxygen, or the like.
  • Thermal initiators that can be used include azo compounds: 1 ,1 '- azobis(cyclohexanecarbonitrile) 98%, azobisisobutyronitrile 12 wt.
  • inorganic peroxides ammonium persulfate reagent grade, 98%; hydroxymethanesulfinic acid monosodium salt dihydrate; potassium persulfate ACS reagent, >99.0%; sodium persulfate reagent grade, >98%; dicumyl peroxide 98%; and organic peroxides: tert- butyl hydroperoxide solution packed in FEP bottles, ⁇ 5.5 M in decane (over molecular sieve 4A); fe/f-butyl hydroperoxide solution 5.0-6.0 M in nonane; tert- butyl peracetate solution 50 wt.
  • % in odorless mineral spirits cumene hydroperoxide technical grade, 80%;2,5-di(fe/f-butylperoxy)-2,5-dimethyl-3-hexyne, blend; Luperox ® 101 , 2,5-bis (tert- butylperoxy)-2,5-dimethylhexane technical grade, 90%; Luperox ® 101XL45, 2,5-bis (tert- butylperoxy)-2,5-dimethylhexane, blend with calcium carbonate and silica;
  • Luperox ® 224 2,4-pentanedione peroxide solution ⁇ 34 wt. % in 4-hydroxy-4-methyl-2- pentanone and A/-methyl-2-pyrrolidone; Luperox ® 231 , 1 ,1 -bis(fe/f-butylperoxy)-3,3,5- trimethylcyclohexane 92%; Luperox ® 331 M80, 1 ,1 -bis(fe/f-butylperoxy)cyclohexane solution ⁇ 80 wt.
  • Luperox ® A98 benzoyl peroxide reagent grade, >98%
  • Luperox ® AFR40 benzoyl peroxide solution 40 wt. % in dibutyl phthalate
  • Luperox ® ATC50 benzoyl peroxide ⁇ 50 wt. % in tricresyl phosphate
  • Luperox ® DDM-9 2-butanone peroxide solution ⁇ 35 wt. % in 2,2,4-trimethyl-1 ,3- pentanediol diisobutyrate
  • Luperox ® DHD-9 2-butanone peroxide solution ⁇ 32 wt. % in phthalate-free plasticizer mixture
  • Luperox ® Dl tert- butyl peroxide 98%
  • Luperox ® P tert- butyl peroxybenzoate 98%
  • Luperox ® TBEC tert- butylperoxy 2- ethylhexyl carbonate 95%
  • Luperox ® TBH70X tert- butyl hydroperoxide solution 70 wt.
  • the weight ratio of the acrylic latex core polymer to the acrylic latex shell polymer can be from 1 :1 to 9:1 (50:50 to 90:10; or 50 wt% core and 50 wt% shell to 90 wt% core to 10 wt% shell). Other weight ratios that can be used include from 60:40 to 90: 10, from 60:40 to 85: 15, from 65:35 to 90: 10, or from 65:35 to 85: 15, for example.
  • the acrylic core-shell latex particles can have any acid number at the surface that is suitable for printing on fabric.
  • the acid number (or acid value) can be relatively low, e.g., from 0 mg KOH/g to 45 mg KOH/g, from 0 mg KOH/g to 30 mg KOH/g, from 2 mg KOH/g to 20 mg KOH/g, or from 4 mg KOH/g to 15 mg KOH/g, for example.
  • the term“acid value” or“acid number” refers to the mass of potassium hydroxide (KOH) in milligrams that can be used to neutralize one gram of substance (mg KOH/g), such as the latex polymers disclosed herein. This value can be determined, in one example, by dissolving or dispersing a known quantity of a material in organic solvent and then titrating with a solution of potassium hydroxide (KOH) of known concentration for measurement.
  • the acrylic core-shell latex particles can have a latex core weight average molecular weight from 30,000 Mw to 1 ,500,000 Mw, from 50,000 Mw to 1 ,000,000 Mw, or from 75,000 Mw to 500,000 Mw. Furthermore, the acrylic core-shell latex particles can have a latex shell weight average molecular weight from 10,000 Mw to 1 ,000,000 Mw, from 20,000 Mw to 500,000 Mw, or from 30,000 Mw to 300,000 Mw.
  • the acrylic shell copolymer can include from 1 wt% to 14 wt% copolymerized acrylic acid, methacrylic acid, or a combination thereof.
  • the copolymerized acrylic acid and/or methacrylic acid can be present at from 2 wt% to 12 wt%, or from 4 wt% to 10 wt%.
  • the acrylic shell copolymer can include from 30 wt% to 80 wt% copolymerized methyl methacrylate, ethyl methacrylate, or a combination thereof.
  • the copolymerized methyl methacrylate and/or ethyl methacrylate can be present at from 35 wt% to 75 wt%, from 40 wt% to 70 wt%, or from 40 wt% to 60 wt%, for example.
  • the methyl methacrylate can be present at from 30 wt% to 80 wt%, at from 35 wt% to 75 wt%, from 40 wt% to 70 wt%, or from 40 wt% to 60 wt%
  • the acrylic shell copolymer can be devoid of ethyl methacrylate.
  • the pigment can be any of a number of pigments of any of a number of primary or secondary colors, or can be black or white, for example. More specifically, colors can include cyan, magenta, yellow, red, blue, violet, red, orange, green, etc.
  • the ink composition can be a black ink with a carbon black pigment.
  • the ink composition can be a cyan or green ink with a copper phthalocyanine pigment, e.g., Pigment Blue 15:0, Pigment Blue 15:1 ; Pigment Blue 15:3, Pigment Blue 15:4, Pigment Green 7, Pigment Green 36, etc.
  • the ink composition can be a magenta ink with a quinacridone pigment or a co-crystal of quinacridone pigments.
  • Example quinacridone pigments that can be utilized can include PR122, PR192, PR202, PR206, PR207, PR209, P048, P049, PV19, PV42, or the like. These pigments tend to be magenta, red, orange, violet, or other similar colors.
  • the quinacridone pigment can be PR122, PR202, PV19, or a combination thereof.
  • the ink composition can be a yellow ink with an azo pigment, e.g., PY74 and PY155.
  • pigments include the following, which are available from BASF Corp.: PALIOGEN® Orange, HELIOGEN® Blue L 6901 F, HELIOGEN® Blue NBD 7010, HELIOGEN® Blue K 7090, HELIOGEN® Blue L 7101 F, PALIOGEN® Blue L 6470, HELIOGEN® Green K 8683, HELIOGEN® Green L 9140, CHROMOPHTAL® Yellow 3G, CHROMOPHTAL® Yellow GR,
  • the following pigments are available from Degussa Corp.: Color Black FWI, Color Black FW2, Color Black FW2V, Color Black 18, Color Black, FW200, Color Black 5150, Color Black S160, and Color Black 5170.
  • the following black pigments are available from Cabot Corp.: REGAL® 400R, REGAL® 330R, REGAL® 660R, MOGUL® L, BLACK PEARLS® L, MONARCH® 1400, MONARCH® 1300, MONARCH® 1100, MONARCH® 1000, MONARCH® 900, MONARCH® 880, MONARCH® 800, and MONARCH® 700.
  • the following pigments are available from Orion Engineered Carbons GMBH:
  • PRINTEX® U PRINTEX® V
  • PRINTEX® 140U PRINTEX® 140V
  • PRINTEX® 35 PRINTEX® 35
  • the following pigment is available from DuPont: TI-PURE® R-101.
  • the following pigments are available from Heubach: MONASTRAL® Magenta, MONASTRAL® Scarlet, MONASTRAL® Violet R, MONASTRAL® Red B, and MONASTRAL® Violet Maroon B.
  • the following pigments are available from Clariant: DALAMAR® Yellow YT-858-D, Permanent Yellow GR, Permanent Yellow G,
  • Permanent Yellow DHG Permanent Yellow NCG-71 , Permanent Yellow GG, Hansa Yellow RA, Hansa Brilliant Yellow 5GX-02, Hansa Yellow-X, NOVOPERM® Yellow HR, NOVOPERM® Yellow FGL, Hansa Brilliant Yellow 10GX, Permanent Yellow G3R-01 , HOSTAPERM® Yellow H4G, HOSTAPERM® Yellow H3G, HOSTAPERM® Orange GR, HOSTAPERM® Scarlet GO, and Permanent Rubine F6B.
  • the following pigments are available from Sun Chemical: QUINDO® Magenta, INDOFAST® Brilliant Scarlet, QUINDO® Red R6700, QUINDO® Red R6713, INDOFAST® Violet, L74-1357 Yellow, L75-1331 Yellow, L75-2577 Yellow, and LHD9303 Black.
  • the following pigments are available from Birla Carbon: RAVEN® 7000, RAVEN® 5750, RAVEN® 5250, RAVEN® 5000 Ultra® II, RAVEN® 2000, RAVEN® 1500, RAVEN® 1250, RAVEN® 1200, RAVEN® 1190 Ultra®.
  • RAVEN® 1170, RAVEN® 1255, RAVEN® 1080, and RAVEN® 1060 are available from Sun Chemical: QUINDO® Magenta, INDOFAST® Brilliant Scarlet, QUINDO® Red R6700, QUINDO® Red R6713, INDOFAST® Violet, L74-1357 Yellow, L75-1331 Yellow, L75
  • the following pigments are available from Mitsubishi Chemical Corp.: No. 25, No. 33, No. 40, No. 47, No. 52, No. 900, No. 2300, MCF-88, MA600, MA7, MA8, and MA100.
  • the colorant may be a white pigment, such as titanium dioxide, or other inorganic pigments such as zinc oxide and iron oxide.
  • a cyan color pigment may include C.l. Pigment Blue -1 , -2, -3, -15, -15:1 ,-15:2, -15:3, -15:4, -16, -22, and -60; magenta color pigment may include C. I. Pigment Red -5, -7, -12, -48, -48: 1 , -57, -112, -122, -123, -146, -168, - 177, -184, -202, and C.l. Pigment Violet-19; yellow pigment may include C.l.
  • Black pigment may include carbon black pigment or organic black pigment such as aniline black, e.g., C.l. Pigment Black 1. While several examples have been given herein, it is to be understood that any other pigment can be used that is useful in color modification, or dye may even be used in addition to the pigment.
  • pigments and dispersants are described separately herein, but there are pigments that are commercially available which include both the pigment and a dispersant suitable for ink composition formulation.
  • pigment dispersions that can be used, which include both pigment solids and dispersant are provided by example, as follows: HPC-K048 carbon black dispersion from DIC
  • the pigment(s) can be dispersed by a dispersant that is adsorbed or ionically attracted to a surface of the pigment, or can be covalently attached to a surface of the pigment as a self-dispersed pigment.
  • the dispersant can be an acrylic dispersant, such as a styrene (meth)acrylate dispersant, or other dispersant suitable for keeping the pigment suspended in the liquid vehicle.
  • the styrene (meth)acrylate dispersant can be used, as it can promote tt-stacking between the aromatic ring of the dispersant and various types of pigments.
  • the styrene (meth)acrylate dispersant can have a weight average molecular weight from 4,000 Mw to 30,000 Mw. In another example, the styrene-acrylic dispersant can have a weight average molecular weight of 8,000 Mw to 28,000 Mw, from 12,000 Mw to 25,000 Mw, from 15,000 Mw to 25,000 Mw, from 15,000 Mw to 20,000 Mw, or about 17,000 Mw. Regarding the acid number, the styrene (meth)acrylate dispersant can have an acid number from 100 to 350, from 120 to 350, from 150 to 300, from 180 to 250, or about 214, for example.
  • Example commercially available styrene-acrylic dispersants can include Joncryl ® 671 , Joncryl ® 71 , Joncryl ® 96, Joncryl ® 680, Joncryl ® 683, Joncryl ® 678, Joncryl ® 690, Joncryl ® 296, Joncryl ® 671 , Joncryl ® 696 or Joncryl ® ECO 675 (all available from BASF Corp., Germany).
  • the ink compositions of the present disclosure can be formulated to include a liquid vehicle, which can include the water content, e.g., 60 wt% to 90 wt% or from 75 wt% to 85 wt%, as well as organic co-solvent, e.g., from 4 wt% to 30 wt%, from 6 wt% to 20 wt%, or from 8 wt% to 15 wt%.
  • Other liquid vehicle components can also be included, such as surfactant, antibacterial agent, other colorant, etc.
  • the pigment, dispersant, and the acrylic core-shell latex particles can be included or carried by the liquid vehicle components.
  • Suitable pH ranges for the ink composition can be from pH 6 to pH 10, from pH 7 to pH 10, from pH 7.5 to pH 10, from pH 8 to pH 10, 6 to pH 9, from pH 7 to pH 9, from pH 7.5 to pH 9, etc.
  • the co-solvent(s) can be present and can include any co-solvent or combination of co-solvents that are
  • solvents such as alcohols, amides, esters, ketones, lactones, and ethers.
  • solvents that can be used can include aliphatic alcohols, aromatic alcohols, diols, glycol ethers, polyglycol ethers, caprolactams, formamides, acetamides, and long chain alcohols.
  • Examples of such compounds include primary aliphatic alcohols, secondary aliphatic alcohols, 1 ,2- alcohols, 1 ,3-alcohols, 1 ,5-alcohols, ethylene glycol alkyl ethers, propylene glycol alkyl ethers, higher homologs (C6-C12) of polyethylene glycol alkyl ethers, N-alkyl
  • organic solvents can include 2-pyrrolidone, 2-ethyl-2-(hydroxymethyl)-1 , 3- propane diol (EPHD), glycerol, dimethyl sulfoxide, sulfolane, glycol ethers, alkyldiols such as 1 ,2-hexanediol, and/or ethoxylated glycerols such as LEG-1 , etc.
  • the liquid vehicle can also include surfactant and/or emulsifier.
  • the surfactant can be water soluble and may include alkyl polyethylene oxides, alkyl phenyl polyethylene oxides, polyethylene oxide (PEO) block copolymers, acetylenic PEO, PEO esters, PEO amines, PEO amides, dimethicone copolyols, ethoxylated surfactants, alcohol ethoxylated surfactants, fluorosurfactants, and mixtures thereof.
  • the surfactant can include a nonionic surfactant, such as a Surfynol® surfactant, e.g., Surfynol® 440 (from Evonik, Germany), or a TergitolTM surfactant, e.g., TergitolTM TMN-6 (from Dow Chemical, USA).
  • the surfactant can include an anionic surfactant, such as a phosphate ester of a C10 to C20 alcohol or a polyethylene glycol (3) oleyl mono/di phosphate, e.g., Crodafos® N3A (from Croda International PLC, United Kingdom).
  • the surfactant or combinations of surfactants can be included in the ink composition at from about 0.01 wt% to about 5 wt% and, in some examples, can be present at from about 0.05 wt% to about 3 wt% of the ink compositions.
  • additives may be included to provide desired properties of the ink composition for specific applications.
  • these additives are those added to inhibit the growth of harmful microorganisms.
  • These additives may be biocides, fungicides, and other microbial agents, which are routinely used in ink formulations.
  • suitable microbial agents include, but are not limited to, Acticide®, e.g., Acticide® B20 (Thor Specialties Inc.), NuoseptTM (Nudex, Inc.), UcarcideTM (Union carbide Corp.), Vancide® (R.T. Vanderbilt Co.), ProxelTM (ICI America), and combinations thereof.
  • Sequestering agents such as EDTA (ethylene diamine tetra acetic acid) or trisodium salt of methylglycinediacetic acid, may be included to eliminate the deleterious effects of heavy metal impurities, and buffer solutions may be used to control the pH of the ink. Viscosity modifiers and buffers may also be present, as well as other additives known to those skilled in the art to modify properties of the ink as desired.
  • ink compositions can be suitable for printing on many types of textiles, but can be particularly acceptable on treated or untreated natural fabric textile substrates, e.g., wool, cotton, silk, linen, jute, flax, hemp, rayon fibers, thermoplastic aliphatic polymeric fibers derived from renewable resources (e.g. cornstarch, tapioca products, sugarcanes), etc.
  • Treated fabrics can include a coating, for example, such as a coating including a cationic component such as calcium salt, magnesium salt, cationic polymer, etc.
  • OD optical density
  • washfastness can be defined as the OD or delta E (DE) that is retained after five (5) standard washing machine cycles using warm water and a standard clothing detergent (e.g., Tide® available from Proctor and
  • AOD and DE value can be determined, which is essentially a quantitative way of expressing the difference between the OD and/or L*a*b*prior to and after undergoing the washing cycles.
  • DO ⁇ and DE values the better.
  • DE is a single number that represents the "distance" between two colors, which in accordance with the present disclosure, is the color (or black) prior to washing and the modified color (or modified black) after washing.
  • Colors for example, can be expressed as CIELAB values. It is noted that color differences may not be symmetrical going in both directions (pre-washing to post washing vs. post-washing to pre-washing). Using the CIE 1976 definition, the color difference can be measured and the DE value calculated based on subtracting the pre washing color values of L* a* and b* from the post-washing color values of L* a* and b*. Those values can then be squared, and then a square root of the sum can be determined to arrive at the DE value.
  • The1976 standard can be referred to herein as “DEOIE.”
  • the CIE definition was modified in 1994 to address some perceptual non uniformities, retaining the L*a*b* color space, but modifying to define the L*a*b* color space with differences in lightness (L*), chroma (C*), and hue (h*) calculated from L*a*b* coordinates.
  • the CIEDE standard was established to further resolve the perceptual non-uniformities by adding five corrections, namely i) hue rotation (RT) to deal with the problematic blue region at hue angles of about 275°), ii) compensation for neutral colors or the primed values in the L*C*h differences, iii) compensation for lightness (SL), iv) compensation for chroma (Sc), and v) compensation for hue (SH).
  • the 2000 modification can be referred to herein as“DE2000.”
  • DE value can be determined using the CIE definition established in 1976, 1994, and 2000 to demonstrate washfastness.
  • DEOIE and DE2000 are used.
  • ink compositions with these acrylic core-shell latex particles can also exhibit good stability over time as well as good thermal inkjet printhead performance such as high drop weight, high drop velocity, good kogation, and acceptable“Turn On Energy” or“TOE” curve values.
  • Turn On Energy can be defined as the measurement of energy used to generate a given ink drop weight (DW) upon firing. The goal is to achieve a consistent ink composition firing at a drop weight at a lower energy. At some point, the DW that increases with energy input starts to flatten out. Examples of TOE curves can be found and described in the
  • the fabric can include a substrate, and in some examples can be treated, such as with a coating that includes a calcium salt, a magnesium salt, a cationic polymer, or a combination of a calcium or magnesium salt and cationic polymer.
  • Fabric substrates can include substrates that have fibers that may be natural and/or synthetic, but in some examples, the fabric is particularly useful with natural fabric substrates.
  • the fabric substrate can include, for example, a textile, a cloth, a fabric material, fabric clothing, or other fabric product suitable for applying ink, and the fabric substrate can have any of a number of fabric structures.
  • fabric structure is intended to include structures that can have warp and weft, and/or can be woven, non-woven, knitted, tufted, crocheted, knotted, and pressured, for example.
  • warp and weft have their ordinary meaning in the textile arts, as used herein, e.g., warp refers to lengthwise or longitudinal yarns on a loom, while weft refers to crosswise or transverse yarns on a loom.
  • Fabric substrate does not include materials commonly known as any kind of paper (even though paper can include multiple types of natural and synthetic fibers or mixtures of both types of fibers).
  • Fabric substrates can include textiles in filament form, textiles in the form of fabric material, or textiles in the form of fabric that has been crafted into a finished article (e.g. clothing, blankets, tablecloths, napkins, towels, bedding material, curtains, carpet, handbags, shoes, banners, signs, flags, etc.).
  • the fabric substrate can have a woven, knitted, non-woven, or tufted fabric structure.
  • the fabric substrate can be a woven fabric where warp yarns and weft yarns can be mutually positioned at an angle of about 90°.
  • This woven fabric can include but is not limited to, fabric with a plain weave structure, fabric with a twill weave structure where the twill weave produces diagonal lines on a face of the fabric, or a satin weave.
  • the fabric substrate can be a knitted fabric with a loop structure.
  • the loop structure can be a warp- knit fabric, a weft-knit fabric, or a combination thereof.
  • a warp-knit fabric refers to every loop in a fabric structure that can be formed from a separate yarn mainly introduced in a longitudinal fabric direction.
  • a weft-knit fabric refers to loops of one row of fabric that can be formed from the same yarn.
  • the fabric substrate can be a non-woven fabric.
  • the non-woven fabric can be a flexible fabric that can include a plurality of fibers or filaments that are one or both bonded together and interlocked together by a chemical treatment process (e.g., a solvent treatment), a mechanical treatment process (e.g., embossing), a thermal treatment process, or a combination of two or more of these processes.
  • the fabric substrate can include natural fibers, synthetic fibers, or a combination thereof.
  • natural fibers can include, but are not limited to, wool, cotton, silk, linen, jute, flax, hemp, rayon fibers, thermoplastic aliphatic polymeric fibers derived from renewable resources (e.g. cornstarch, tapioca products, sugarcanes), or a combination thereof.
  • the fabric substrate can include synthetic fibers.
  • Exemplary synthetic fibers can include polymeric fibers such as, polyvinyl chloride (PVC) fibers, PVC-free fibers made of polyester, polyamide, polyimide, polyacrylic, polypropylene, polyethylene, polyurethane, polystyrene, polyaramid (e.g., Kevlar ® ) polytetrafluoroethylene (Teflon ® ) (both trademarks of E. I. du Pont de Nemours Company, Delaware), fiberglass, polytrimethylene, polycarbonate, polyethylene terephthalate, polyester terephthalate, polybutylene terephthalate, or a combination thereof.
  • the synthetic fiber can be a modified fiber from the above-listed polymers.
  • the term“modified fiber” refers to one or both of the polymeric fiber and the fabric as a whole having undergone a chemical or physical process such as, but not limited to, one or more of a
  • PVC-free fibers means that no polyvinyl chloride (PVC) polymer or vinyl chloride monomer units are in the fibers.
  • the fabric substrate can be a combination of fiber types, e.g. a combination of any natural fiber with another natural fiber, any natural fiber with a synthetic fiber, a synthetic fiber with another synthetic fiber, or mixtures of multiple types of natural fibers and/or synthetic fibers in any of the above combinations.
  • the fabric substrate can include natural fiber and synthetic fiber.
  • the amount of each fiber type can vary.
  • the amount of the natural fiber can vary from about 5 wt% to about 95 wt% and the amount of synthetic fiber can range from about 5 wt% to 95 wt%.
  • the amount of the natural fiber can vary from about 10 wt% to 80 wt% and the synthetic fiber can be present from about 20 wt% to about 90 wt%. In other examples, the amount of the natural fiber can be about 10 wt% to 90 wt% and the amount of synthetic fiber can also be about 10 wt% to about 90 wt%.
  • the ratio of natural fiber to synthetic fiber in the fabric substrate can vary. For example, the ratio of natural fiber to synthetic fiber can be 1 : 1 , 1 :2, 1 :3, 1 :4,
  • the fabric substrate can have a basis weight ranging from about 10 gsm to about 500 gsm. In another example, the fabric substrate can have a basis weight ranging from about 50 gsm to about 400 gsm. In other examples, the fabric substrate can have a basis weight ranging from about 100 gsm to about 300 gsm, from about 75 gsm to about 250 gsm, from about 125 gsm to about 300 gsm, or from about 150 gsm to about 350 gsm.
  • the fabric substrate can contain additives including, but not limited to, one or more of colorant (e.g., pigments, dyes, and tints), antistatic agents, brightening agents, nucleating agents, antioxidants, UV stabilizers, fillers and lubricants, for example.
  • colorant e.g., pigments, dyes, and tints
  • antistatic agents e.g., antistatic agents, brightening agents, nucleating agents, antioxidants, UV stabilizers, fillers and lubricants
  • the fabric substrate may be pre-treated in a solution containing the substances listed above before applying other treatments or coating layers.
  • a method 200 of textile printing includes jetting 210 an aqueous ink composition onto a fabric substrate.
  • the aqueous ink composition in this example includes an aqueous ink vehicle, pigment, and from 2 wt% to 15 wt% of acrylic core-shell latex particles having an acrylic core copolymer with a glass transition temperature from -50 °C to 30 °C and an acrylic shell copolymer having a glass transition temperature from 50 °C to 130 °C.
  • the acrylic core copolymer and the acrylic shell copolymer of the acrylic core-shell latex particles have an average weight ratio from 1 :1 to 9:1 in this example.
  • the method can include heating the fabric substrate with the aqueous ink composition thereon to a temperature ranging from above the glass transition temperature of the acrylic shell copolymer to 200 °C.
  • the fabric substrate can include, for example, cotton, polyester, nylon, silk, or a blend thereof.
  • the term“about” is used to provide flexibility to a numerical range endpoint by providing that a given value may be“a little above” or“a little below” the endpoint.
  • the degree of flexibility of this term can be dictated by the particular variable and would be within the knowledge of those skilled in the art to determine based on experience and the associated description herein.
  • a weight ratio range of about 1 wt% to about 20 wt% should be interpreted to include not only the explicitly recited limits of about 1 wt% and about 20 wt%, but also to include individual weights such as 2 wt%, 11 wt%, 14 wt%, and sub-ranges such as 10 wt% to 20 wt%, 5 wt% to 15 wt%, etc.
  • a seed latex (Seed Latex 1 ) was obtained to use as a common seed latex for the preparation of several acrylic core-shell latexes of several examples hereinafter.
  • the seed latex was selected to control particle size of the core-shell latex prepared in accordance with the examples hereinafter, e.g., Examples 2-19 (Latexes 2-19).
  • the seed latex was an all acrylic latex copolymer with a D50 particle size of approximately 65 nm (diameter) and a solids content of approximately 48 wt%.
  • Tables 1 A-1 C below summarize the acrylic latexes prepared in Examples 2-19, including the amount of first stage (core) and second stage (shell) monomers used as a percentage of the total monomer of the formulations.
  • Examples 13 and 14 are single-phase acrylic latexes, so they are considered to be 100 wt% core, as notated in the summary tables below.
  • the details on the Seed Latex are not included in the Tables.
  • the examples were either dual-phase preparations to generate acrylic core-shell latex particles (first stage core varied wt% from 65 wt% to 85 wt; second stage shell varied wt% from 15 wt% to 35 wt%); or single-phase (100 wt% first stage monomer).
  • the calculated glass transition temperature (Tg) for the core and the shell (separately) were included, which can be calculated based on the Fox equation using homopolymer Tg values shown in Table 2.
  • Theoretical acid values and measured solid percentages were also provided for the completed acrylic latex polymer particles.
  • Table 1 A - Summary of Examples 2-8 Acrylic Latex Polymer Particles (Latexes 2-8)
  • the first monomer feed was fed over 150 minutes [149.8 grams n-butyl acrylate (BA), 123.2 grams styrene, 13.7 grams Hitenol AR-1025 (polyoxyethylene styrenated phenyl ether ammonium sulfate anionic
  • the first monomer feed was fed over 150 minutes [136.8 n-butyl acrylate (BA), 112.6 grams styrene, 12.5 grams Hitenol AR-1025 (polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant) and 53.2 grams water].
  • BA n-butyl acrylate
  • Hitenol AR-1025 polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant
  • the reactor was held at 77 °C for 30 minutes, and then the second monomer feed was fed over 90 minutes [98.6 grams methyl methacrylate (MMA), 20.2 grams styrene, 6.7 grams n-butyl acrylate (BA), 8.1 grams methacrylic acid (MAA), 0.7 grams iso-octyl thioglycolate (i-OTG), 6.9 grams Hitenol AR-1025 and 27.1 grams water].
  • Ten minutes after the end of the second monomer feed 75.3 grams of a 5 wt% solution of KOH in water was fed to the reactor over 10 minutes and then the reactor was held at 77 °C for another 30 minutes.
  • the first monomer feed was fed over 150 minutes [173.3 n-butyl acrylate (BA), 142.6 grams styrene, 15.8 grams Hitenol AR-1025 (polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant) and 67.3 grams water].
  • BA n-butyl acrylate
  • Hitenol AR-1025 polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant
  • the reactor was held at 77 °C for 30 minutes, and then the second monomer feed was fed over 90 minutes [40.9 grams methyl methacrylate (MMA), 8.4 grams styrene, 2.8 grams n-butyl acrylate (BA), 3.4 grams methacrylic acid (MAA), 0.3 grams iso-octyl thioglycolate (i-OTG), 2.9 grams Hitenol AR-1025 and 11.3 grams water].
  • Ten minutes after the end of the second monomer feed 41 grams of a 5 wt% solution of KOH in water was fed to the reactor over 10 minutes and then the reactor was held at 77 °C for another 30 minutes.
  • the first monomer feed was fed over 150 minutes [149.3 n-butyl acrylate (BA), 122.9 grams styrene, 2.7 grams of butanediol diacrylate (BDDA), 13.6 grams Hitenol AR-1025 (polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant) and 58 grams water].
  • BA n-butyl acrylate
  • BDDA butanediol diacrylate
  • Hitenol AR-1025 polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant
  • the reactor was held at 77 °C for 30 minutes, and then the second monomer feed was fed over 90 minutes [66.1 grams methyl methacrylate (MMA), 13.7 grams styrene, 4.6 grams n-butyl acrylate (BA), 5.5 grams methacrylic acid (MAA), 0.5 gram iso-octyl thioglycolate (i-OTG), 4.7 grams Hitenol AR-1025 and 18.3 grams water].
  • MMA methyl methacrylate
  • BA n-butyl acrylate
  • MAA methacrylic acid
  • i-OTG 0.5 gram iso-octyl thioglycolate
  • Hitenol AR-1025 4.7 grams Hitenol AR-1025 and 18.3 grams water.
  • the first monomer feed was fed over 150 minutes [137.6 grams n-butyl acrylate (BA), 122.2 grams styrene, 10.9 grams diacetone acrylamide (DAAM), 13.6 grams Hitenol AR-1025 (polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant) and 57.7 grams water].
  • BA n-butyl acrylate
  • DAAM diacetone acrylamide
  • Hitenol AR-1025 polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant
  • the first monomer feed was fed over 150 minutes [144.3 grams n-butyl acrylate (BA), 123.2 grams styrene, 5.5 grams of
  • Sipomer® WAMII allyl ether of a substituted urea co-monomer from Solvay, Belgium
  • Hitenol AR-1025 polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant
  • the reactor was held at 77 °C for 30 minutes, and then the second monomer feed was fed over 90 minutes [65 grams methyl methacrylate (MMA), 13.7 grams styrene, 4.6 grams n-butyl acrylate (BA), 3.7 grams methacrylic acid (MAA), 0.5 gram iso-octyl thioglycolate (i-OTG), 3.7 grams Sipomer® WAMII, 4.7 grams Hitenol AR-1025 and 18.4 grams water].
  • MMA methyl methacrylate
  • BA n-butyl acrylate
  • MAA methacrylic acid
  • i-OTG 0.5 gram iso-octyl thioglycolate
  • Sipomer® WAMII 3.7 grams Sipomer® WAMII
  • the first monomer feed was fed over 150 minutes [190.9 n-butyl acrylate (BA), 82.2 grams styrene, 13.7 grams Hitenol AR-1025 (polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant) and 58.2 grams water].
  • BA n-butyl acrylate
  • Hitenol AR-1025 polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant
  • the reactor was held at 77 °C for 30 minutes, and then the second monomer feed was fed over 90 minutes [68.6 grams methyl methacrylate (MMA), 13.7 grams styrene, 4.6 grams n-butyl acrylate (BA), 3.7 grams methacrylic acid (MAA), 0.5 gram iso-octyl thioglycolate (i-OTG), 4.7 grams Hitenol AR-1025 and 18.4 grams water].
  • MMA methyl methacrylate
  • BA n-butyl acrylate
  • MAA methacrylic acid
  • i-OTG 0.5 gram iso-octyl thioglycolate
  • Hitenol AR-1025 4.7 grams Hitenol AR-1025 and 18.4 grams water.
  • the first monomer feed was fed over 150 minutes [164.9 n-butyl acrylate (BA), 71 grams styrene, 11.8 grams Hitenol AR-1025 (polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant) and 50.3 grams water].
  • BA n-butyl acrylate
  • Hitenol AR-1025 polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant
  • the reactor was held at 77 °C for 30 minutes, and then the second monomer feed was fed over 90 minutes [95.8 grams methyl methacrylate (MMA), 19.1 grams styrene, 6.4 grams n-butyl acrylate (BA), 5.1 grams methacrylic acid (MAA), 0.6 grams iso-octyl thioglycolate (i-OTG), 6.6 grams Hitenol AR-1025 and 25.6 grams water].
  • Ten minutes after the end of the second monomer feed 64.5 grams of a 5 wt% solution of KOH in water was fed to the reactor over 10 minutes and then the reactor was held at 77 °C for another 30 minutes.
  • the first monomer feed was fed over 150 minutes [216.2 n-butyl acrylate (BA), 93.1 grams styrene, 15.5 grams Hitenol AR-1025 (polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant) and 65.9 grams water].
  • BA n-butyl acrylate
  • Hitenol AR-1025 polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant
  • the first monomer feed was fed over 150 minutes [185.4 grams n-butyl acrylate (BA), 82.2 grams styrene, 5.5 grams of Sipomer® WAMII (allyl ether of a substituted urea co-monomer from Solvay, Belgium), 13.7 grams Hitenol AR-1025 (polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant) and 58.2 grams water].
  • BA n-butyl acrylate
  • SA styrene
  • Sipomer® WAMII allyl ether of a substituted urea co-monomer from Solvay, Belgium
  • Hitenol AR-1025 polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant
  • the first monomer feed was fed over 150 minutes [163.5 grams n-butyl acrylate (BA), 139.6 grams styrene, 6.2 grams of
  • Sipomer® WAMII allyl ether of a substituted urea co-monomer from Solvay, Belgium
  • Hitenol AR-1025 polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant
  • the reactor was held at 77 °C for 30 minutes, and then the second monomer feed was fed over 90 minutes [39 grams methyl methacrylate (MMA), 8.2 grams styrene, 2.7 grams n-butyl acrylate (BA), 2.2 grams methacrylic acid (MAA), 0.3 grams iso-octyl thioglycolate (i-OTG), 2.2 grams Sipomer® WAMII, 2.8 grams Hitenol AR-1025 and 11 grams water].
  • MMA methyl methacrylate
  • BA n-butyl acrylate
  • MAA methacrylic acid
  • i-OTG iso-octyl thioglycolate
  • Sipomer® WAMII 2.8 grams Hitenol AR-1025 and 11 grams water.
  • the pH was 8.1
  • the solids content was 37.3 wt%.
  • the monomer feed was fed over 150 minutes [195.9 grams n-butyl acrylate (BA), 164.2 grams styrene, 3.65 grams methacrylic acid (MAA), 18.2 grams Hitenol AR-1025 (polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant) and 77.5 grams water] and afterwards the reactor was held at 77 °C for 30 minutes.
  • BA n-butyl acrylate
  • MAA methacrylic acid
  • Hitenol AR-1025 polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant
  • the monomer feed was fed over 150 minutes [250.6 grams n-butyl acrylate (BA), 109.4 grams styrene, 3.7 grams methacrylic acid (MAA), 18.2 grams Hitenol AR-1025 (polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant) and 77.5 grams water] and afterwards the reactor was held at 77 °C for 30 minutes.
  • BA n-butyl acrylate
  • MAA methacrylic acid
  • Hitenol AR-1025 polyoxyethylene styrenated phenyl ether ammonium sulfate anionic surfactant
  • the reaction mixture was kept at 80 °C for an additional 1 hour to allow it for continuing polymerization. After that, 15.174 grams of styrene, 0.317 grams of sodium persulfate, 0.5 gram of sodium dodecyl sulfate, 0.168 of 2-ethylhexyl acrylate (EHA),1.575 grams of methacrylic acid (MAA), 0.468 grams of n- butyl acrylate (BA), and 7.299 grams of methyl methacrylate (MMA) in 38 grams Dl water were mixed and added to the reactor within 1 hr. The reaction mixture was continuously stirred at 80 °C for 3 hours.
  • a mixture of 14.919 grams of styrene, 0.375 grams of sodium persulfate, 1.5 grams of sodium dodecyl sulfate, 15.839 grams of 2-ethylhexyl acrylate (EHA), 2.374 grams of acrylic acid (AA), 14.688 grams of n-butyl acrylate (BA) and 24.401 grams of methyl methacrylate (MMA) in 111 grams of Dl water were mixed thoroughly and then pumped into the flask for a duration of 1.5 hours. The reaction mixture was kept at 80 °C for an additional 1 hour to allow it for continuing polymerization.
  • MAAM methacrylamide
  • BA n-butyl acrylate
  • MMA methyl methacrylate
  • the latex was filtered through 400 mesh stainless sieve.
  • the D50 particle size measured by Malvern Zetasizer was 178.2 nm (diameter), the pH was 11 , and the solids content was 26.77 wt%.
  • Magenta (M) ink compositions were prepared in accordance with the general formulations shown in Tables 3, with the Latex Polymer (2-19) being the only component modified.
  • the Ink ID numbering hereinafter refers to the Ink formulation of Table 3 combined with the specific Latex Polymer ID number used to prepare the ink composition.
  • Latex 2 corresponds to Ink 2
  • Latex 5 corresponds to Ink 5, and so forth.
  • CrodafosTM N3A is available from Croda International Pic. (Great Britain).
  • Surfynol® 440 is available from Evonik, (Germany).
  • Acticide® B20 is available from Thor Specialties, Inc. (USA).
  • Example 21 Ink Composition Stability
  • Example 20 Teen of the Ink Compositions (listed in Table 4 below) prepared in accordance with Example 20 were evaluated for particle stability. The stability data was collected and evaluated based on accelerated shelf-life (ASL) testing, where the ink compositions were evaluated at the time of formulation, and then subjected to 1 week of elevated temperature (60 °C), and then the same data was collected to see what had changed.
  • ASL accelerated shelf-life
  • Ink Compositions prepared in accordance with Example 20 were evaluated for print performance. Additionally, for comparison, a Control Ink Composition was prepared using a commercially available acrylic latex binder (Jantex® 924 - styrene butyl acrylic polymer binder; 320,000 Mw; Acid Number 17.4; Tg -15 °C; available from Jantex Inks, USA). Print performance evaluations were based on jetting from a thermal inkjet pen (A3410, available from HP, Inc.), and the data collected based on several parameters, including:
  • Decap is determined using the indicated time (1 second or 7 seconds) where nozzles remain open (uncapped), and then the number of lines missing during a print event are recorded. Thus, the lower the number the better for decap performance
  • Percent Missing Nozzles which is calculated based on the number of nozzles incapable of firing at the beginning of a jetting sequence as a percentage of the total number of nozzles on an inkjet printhead attempting to fire.
  • percentage number the higher the percentage number, the better the Percent Missing Nozzles value.
  • Drop Weight which is an average drop weight in nanograms (ng) across the number of nozzles fired measured using a burst mode or firing at 30 kHz.
  • Drop Weight 2,000 (DW 2K), which is measured using a 2-drop mode of firing, firing 2,000 drops and then measuring/calculating the average ink composition drop weight in nanograms (ng) at 30 kHz.
  • Drop Velocity which measures an average velocity of the drop as initially fired from the thermal inkjet nozzles measured in meters per second (m/s).
  • composition firing 0 indicates no drop velocity loss. A positive number indicates how much drop velocity was lost.“Miss” indicates missing, where data was not collectable.
  • low drop volume is also notated for informational purposes, as low drop volumes can be acceptable in some circumstances.
  • achieving a drop weight (DW) of 10 ng or above at an energy level 0.75 Joule may be considered“Good” TOE (with DW getting larger with more energy input until the curve flattens out) for this particular ink composition.
  • Achieving a drop weight (DW) of 8 ng or above at an energy level 0.75 Joule may be considered“Acceptable” TOE (with DW getting larger with more energy input until the curve flattens out).
  • lower drop weights (DW) below 8 ng or even below 7 ng at 0.75 Joules may provide for a“Good” TOE as long as the drop weights continue to get larger as the energy increases and then flatten out at an acceptable drop weight.
  • Achieving a drop weight below 7 ng at an energy level of 0.75 Joule may be considered“Good” TOE (with DW getting larger with more energy input until the curve flattens out, as long as the drop weight is acceptable for inkjet printing applications).
  • Example 20 were evaluated for washfastness durability when printed on fabric.
  • Control Ink was prepared using a commercially available acrylic latex binder (Jantex® 924 - styrene butyl acrylic polymer binder; 320,000 Mw; Acid Number 17.4; Tg 15 °C; available from Jantex Inks, USA).
  • the Ink Compositions were jetted (3 dots per pixel or“dpp”) onto gray cotton fabric print media at 20 grams per meter (gsm) using a thermal inkjet pen (A3410, available from HP, Inc.). Individual samples were cured at either 80 °C or at 150 °C for 3 minutes. Printed samples were washed 5 times with a conventional washer at 40 °C with detergent and air drying between each wash.
  • Example 24 Acrylic Core/Shell Latex Particles vs. Acrylic Single-phase Latex Particles
  • Printability with respect to Turn On Energy can be evaluated using a TOE curve, where the amount of energy (Joules) was evaluated to determine where a more consistent ink composition firing at a drop weight (DW) can be achieved. With this evaluation, higher drop weights achieved at lower energy levels is considered good. At some point the drop weight levels off so that more energy does not generate a greater drop weight. At the location on the TOE curve where an acceptable drop weight is achieved, and where it is starting to flatten out, can indicate an ink composition that has a desirable TOE curve. Stated another way, higher TOE curve is better, meaning higher drop weight at a given firing energy input level. With this analysis, it was found that adding even a thin acrylic latex polymer shell to a latex polymer core tended to increase drop weight and reduce energy input.
  • FIG. 3 The data collected for six (6) different ink compositions is shown in FIG. 3. Two of the ink compositions (Ink 13 and Ink 14) included acrylic single-phase latex particles, and the remaining four ink compositions (Ink 2, Ink 3, Ink 4, and Ink 10) included acrylic core/shell latex particles. As can be seen in the data, in all four cases, the higher curves were with the ink compositions with the core/shell latex particles.
  • the TOE curve of Ink 10 can be compared to the TOE curve of Ink 14.
  • These two ink compositions include a latex with the same acrylic latex core (Latex 14 is 100 wt%“core”; Latex 10 includes the same core with a 15 wt% shell thereon), and the TOE curve for Ink 10 is better at every point along the curve where the curve starts to flatten out (shown in FIG. 3 at (B) with an expanded Y- axis to more fully show the separation between the respective TOE curves).
  • Ink 13 Another comparison to consider is to compare Ink 13 with 100 wt% acrylic single-phase latex particles to Inks 2-4, which include different weight percentages of acrylic shell, but are otherwise similar (except that the methacrylic acid is included in the “core” of Ink 13 to provide dispensability). More specifically, Ink 2 included 25 wt% shell polymer, Ink 3 included 35 wt% shell polymer, and Ink 4 included 15 wt% shell polymer. The Ink that performed the best in the TOE curve analysis was Ink 3, which had the thickest acrylic shell, but even at 15 wt% shell as in Ink 4, the TOE curve was better than with Ink 13.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Ink Jet Recording Methods And Recording Media Thereof (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

Un ensemble de matériau d'impression textile comprend un substrat de tissu et une composition d'encre aqueuse. La composition d'encre aqueuse comprend un véhicule constitué d'encre aqueuse, un pigment, et de 2 % en poids à 15 % en poids de particules de latex à structure coeur-écorce acrylique présentant un coeur copolymère acrylique présentant une température de transition vitreuse de -50 °C à 30 °C et une écorce copolymère acrylique présentant une température de transition vitreuse de 50 °C à 130 °C. Le coeur copolymère acrylique et l'écorce copolymère acrylique des particules de latex à structure coeur-écorce acrylique dans cet exemple sont présents dans un rapport pondéral moyen de 1 : 1 à 9 : 1.
PCT/US2019/016487 2019-02-04 2019-02-04 Impression sur textile WO2020162873A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US17/416,412 US20220074134A1 (en) 2019-02-04 2019-02-04 Textile printing
PCT/US2019/016487 WO2020162873A1 (fr) 2019-02-04 2019-02-04 Impression sur textile

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US2019/016487 WO2020162873A1 (fr) 2019-02-04 2019-02-04 Impression sur textile

Publications (1)

Publication Number Publication Date
WO2020162873A1 true WO2020162873A1 (fr) 2020-08-13

Family

ID=71948268

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2019/016487 WO2020162873A1 (fr) 2019-02-04 2019-02-04 Impression sur textile

Country Status (2)

Country Link
US (1) US20220074134A1 (fr)
WO (1) WO2020162873A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2024018328A (ja) * 2022-07-29 2024-02-08 コニカミノルタ株式会社 捺染用インクジェットインク及び画像形成方法

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1157345A (en) * 1965-10-07 1969-07-09 Rohm & Haas Acrylic Elastomers
GB1467292A (en) * 1973-04-27 1977-03-16 Ugine Kuhlmann Pigmentary printing pastes for textiles
US6698879B1 (en) * 1998-03-19 2004-03-02 Color Wings B.V. Printing textile using an inkjet printer
US20070040879A1 (en) * 2003-03-25 2007-02-22 Kwang-Choon Chung Pretreatment method and apparatus of textile applying inkjet printer, digital textile printing method and apparatus comprising it
US20090293209A1 (en) * 2003-03-25 2009-12-03 Inktec Co., Ltd. Textile printing method and apparatus applying inkjet printer
US20180305863A1 (en) * 2015-10-19 2018-10-25 Fujifilm Imaging Colorants, Inc. Ink-Jet Printing Process

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6936075B2 (en) * 2001-01-30 2005-08-30 Milliken Textile substrates for image printing
US7037346B2 (en) * 2001-10-22 2006-05-02 Milliken & Company Textile substrate having coating containing multiphase fluorochemical and cationic material thereon for image printing
JPWO2003054288A1 (ja) * 2001-12-20 2005-04-28 株式会社デンエンチョウフ・ロマン 捺染方法、捺染用前処理液及び捺染用繊維シート
US7086732B2 (en) * 2003-07-28 2006-08-08 Hewlett-Packard Development Company, L.P. Porous fusible inkjet media with fusible core-shell colorant-receiving layer
WO2005103369A1 (fr) * 2004-04-23 2005-11-03 Huntsman Advanced Materials (Switzerland) Gmbh Procede de teinture ou d'impression de materiaux textiles
JP4969578B2 (ja) * 2005-09-15 2012-07-04 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー ホワイトインクおよびカラーインクを用いた、織物のデジタル印刷

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1157345A (en) * 1965-10-07 1969-07-09 Rohm & Haas Acrylic Elastomers
GB1467292A (en) * 1973-04-27 1977-03-16 Ugine Kuhlmann Pigmentary printing pastes for textiles
US6698879B1 (en) * 1998-03-19 2004-03-02 Color Wings B.V. Printing textile using an inkjet printer
US20070040879A1 (en) * 2003-03-25 2007-02-22 Kwang-Choon Chung Pretreatment method and apparatus of textile applying inkjet printer, digital textile printing method and apparatus comprising it
US20090293209A1 (en) * 2003-03-25 2009-12-03 Inktec Co., Ltd. Textile printing method and apparatus applying inkjet printer
US20180305863A1 (en) * 2015-10-19 2018-10-25 Fujifilm Imaging Colorants, Inc. Ink-Jet Printing Process

Also Published As

Publication number Publication date
US20220074134A1 (en) 2022-03-10

Similar Documents

Publication Publication Date Title
US7354476B2 (en) Inkjet ink composition
US11332633B2 (en) Textile printing
WO2020162873A1 (fr) Impression sur textile
US20210171790A1 (en) Textile printing
WO2020131027A1 (fr) Ensembles de fluides
US20210164158A1 (en) Textile printing
US20210310189A1 (en) Textile printing
EP3694935A1 (fr) Ensembles de fluides
EP3924548B1 (fr) Fluides fixateurs
US20220073769A1 (en) Inkjet ink for textile printing
US11254832B2 (en) Fluid sets
US20210301168A1 (en) Fluid sets
WO2020122954A1 (fr) Impression sur textile
US20220042243A1 (en) Ink compositions with polyurethane binder
US20220348776A1 (en) Ink compositions with polyurethane binder
US20220325135A1 (en) Ink compositions with biodegradable polyurethane binder
US20210363695A1 (en) Textile printing
US20230064522A1 (en) Fixer fluids
US20210309874A1 (en) Textile printing
US20220127787A1 (en) Inkjet printing
US20200277507A1 (en) Aqueous ink compositions

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 19914212

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 19914212

Country of ref document: EP

Kind code of ref document: A1