CN103131003B - 官能基化大豆油化合物、及包含其的涂布组合物 - Google Patents
官能基化大豆油化合物、及包含其的涂布组合物 Download PDFInfo
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- 239000003549 soybean oil Substances 0.000 title claims abstract description 85
- 150000001875 compounds Chemical class 0.000 title claims abstract description 69
- 239000008199 coating composition Substances 0.000 title claims abstract description 65
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 31
- 239000001257 hydrogen Substances 0.000 claims abstract description 31
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 claims abstract description 11
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 10
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 6
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- 150000002431 hydrogen Chemical class 0.000 claims description 19
- 239000000178 monomer Substances 0.000 claims description 16
- 229910052809 inorganic oxide Inorganic materials 0.000 claims description 15
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 14
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 8
- 239000003086 colorant Substances 0.000 claims description 5
- 239000000377 silicon dioxide Substances 0.000 claims description 5
- 229960001866 silicon dioxide Drugs 0.000 claims description 5
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- -1 isobutyl- Chemical group 0.000 claims description 4
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
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- 238000005481 NMR spectroscopy Methods 0.000 description 2
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 2
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- WKBKHYAWTYMMAA-UHFFFAOYSA-N CCC(C)(C)OC(C1C(COCOI)C=CCC1)=O Chemical compound CCC(C)(C)OC(C1C(COCOI)C=CCC1)=O WKBKHYAWTYMMAA-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
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- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- 150000008062 acetophenones Chemical class 0.000 description 1
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- 239000013543 active substance Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
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- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
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- 238000010894 electron beam technology Methods 0.000 description 1
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- 230000007613 environmental effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
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- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
- C11C3/006—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by oxidation
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- C—CHEMISTRY; METALLURGY
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- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
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- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
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Abstract
本发明提供一种官能基化大豆油化合物、及包含其的涂布组合物。该官能基化大豆油化合物具有如式(I)所示结构:式(I)其中,n是各自独立的整数,介于1-10之间;m是各自独立的整数,介于1-10之间;x是各自独立的整数,为1或2;R1是各自独立的取代基,为羟基、 其中i为1或2,j为介于4-60之间的整数,R2为氢、C1-3的烷基、或是丙烯基,R3及R4为氢,或者R3及R4连接在一起而与其所连接的碳原子共同形成一饱和或不饱和六元环,R5、R6、及R7是各自独立的取代基,且为氢、或C1-6的烷基,其中式(I)所示结构中仅有一R1为至少一R1为至少一R1为
Description
技术领域
本发明是涉及一种官能基化大豆油化合物、及包含其的涂布组合物,且特别是涉及一种具有高环境友善度的官能基化大豆油化合物、包含其的涂布组合物。
背景技术
随着经济的蓬勃发展,各式各样油墨的需求日益增加。溶剂型油墨由于具有与基板的附着性佳、且可以通过溶剂去除以回收基板等优点,在工业上被广泛的使用。不过,由于溶剂型油墨有易造成污染(溶剂挥发)以及耗能(需要烘干)等问题,基于环保节能的诉求下,在油墨的研究已逐渐由传统的溶剂型油墨转向UV硬化型油墨。
然而,传统UV硬化型油墨因硬化速度快,使得其与基板的附着性不佳。为了解决上问题,业界提出具有高附着性的UV硬化型油墨,然而,由于油墨无法使用溶剂轻易去除,使得已涂布高附着性UV硬化型油墨的基板无法重复使用,增加废品产生,提高生产成本及环境污染。另一方面,已知UV硬化型油墨所使用的原料一般是为化学的材料,无法被生物所分解,具有较差的环境友善度。
因此,业界需要一种环境友善度高、对基板具有高附着性、且易于移除的UV硬化型油墨。
发明内容
本发明的目的在于提供一种环境友善度高的官能基化大豆油化合物,其用于涂布组合物的组分时对基板具有高附着性且易于被移除。
本发明提出一种官能基化大豆油化合物,其具有如式(I)所示结构:
式(I)
其中,n是各自独立的整数,介于1-10之间;m是各自独立的整数,介于1-10之间;x是各自独立的整数,为1或2;R1是各自独立的取代基,为羟基、 其中i为1或2,j为介于4-60之间的整数,R2为氢、C1-3的烷基、或是丙烯基,R3及R4为氢,或者R3及R4连接在一起而与其所连接的碳原子共同形成一饱和或不饱和六元环,R5、R6、及R7是各自独立的取代基,且为氢、或C1-6的烷基,
其中式(I)所示结构中仅有一R1为至少一R1为至少一R1为
本发明亦提供一种涂布组合物,根据本发明另一实施方式,该涂布组合物可包含一光引发剂;以及上述具有式(I)结构的官能基化大豆油化合物。此外,根据本发明其它实施方式,该涂布组合物可包含一光引发剂;一亚克力单体;一无机氧化物颗粒;以及,上述具有式(I)结构的官能基化大豆油化合物。本发明所述的涂布组合物可利用平板印刷、网版印刷、涂布、喷涂等方式制造成膜,且该涂布组合物可作为一般涂料、消光涂料、防炫光涂料、扩散膜涂料、导光板油墨涂料等。
本发明的优点在于:由于本发明的化合物的主体为大豆油,因此该生质化合物具有高的环境友善度。此外,本发明的官能基化大豆油化合物,是将一环氧大豆油上的环氧基开环,并导入长链氧烷基、羧酸基、以及亚克力基所得。长链氧烷基的导入可是增加化合物的亲水性以及对基材的附着度;羧酸基的导入是增加化合物的碱水可溶性;亚克力基团的导入可使化合物具有可进行光硬化的能力。再者,本发明所述的包含该官能基化大豆油化合物的涂布组合物,可进一步通过控制羧酸基的含量来达到同时具有耐水性、却可以碱水去除的特性,以使得被涂布的基材可回收再利用。
为让本发明的上述和其它目的、特征、和优点能更明显易懂,下文特举出较佳实施例,并配合所附附图,作详细说明如下:
附图说明
图1为实施例1所得的官能基化大豆油化合物1的核磁共振光谱分析。
具体实施方式
本发明是公开一种官能基化大豆油化合物,以及包含该官能基化大豆油化合物的涂布组合物。该官能基化大豆油化合物,其具有如式(I)所示结构:
式(I)
其中,n是各自独立的整数,介于1-10之间;m是各自独立的整数,介于1-10之间;x是各自独立的整数,为1或2;R1是各自独立的取代基,为羟基、 其中i为1或2,j为介于4-60之间的整数,R2为氢、C1-3的烷基、或是丙烯基,R3及R4为氢,或者R3及R4连接在一起而与其所连接的碳原子共同形成一饱和或不饱和六元环,R5、R6、及R7是各自独立的取代基,且为氢、或C1-6的烷基。值得注意的是,为增加该官能基化大豆油化合物与一基材之间的附着力,式(I)所示结构中的一R1需为(其中i为1或2,j为介于4-60之间的整数,R2为氢、C1-3的烷基、或是丙烯基,R3、及R4为氢,或者R3及R4连接在一起而与其所连接的碳原子共同形成一饱和或不饱和六元环);此外,为使该官能基化大豆油化合物具有光可聚合能力,式(I)所示结构中至少一R1可为(R5为氢、或C1-6的烷基);再者,为使该官能基化大豆油化合物可溶于碱水(例如5wt%的NaOH水溶液),式(I)所示结构中至少一R1可为(R6及R7为氢、或C1-6的烷基)。根据本发明另一实施例,为增加该官能基化大豆油化合物的光可聚合能力,具有式(I)所示结构的官能基化大豆油化合物,仅有一R1为(例如 )、至少一R1为(例如)、而其它R1皆为(例如),其中i为1、或2,j为介于4-60之间的整数,R2为氢、C1-3的烷基、或是丙烯基,R3及R4为氢,或者R3及R4连接在一起而与其所连接的碳原子共同形成一饱和或不饱和六元环(例如苯基(phenyl)、或吡啶基(pyridyl)),R5、R6、及R7是各自独立的取代基,且为氢、或C1-6的烷基(例如:甲基、乙基、丙基、异丙基、丁基、异丁基、戊基、或己基)。由于该化合物的主体为大豆油,因此该生质化合物具有高的环境友善度。
本发明还公开一种涂布组合物,可包含一光引发剂;以及,上述的具有式(I)结构的官能基化大豆油化合物。其中,该光引发剂,是指在一能量(如可见光、紫外光、深紫外光、电子束、或X射线时)照射时,可产生引发交联反应的活性物质(例如,自由基、阳离子或阴离子等)。其它的光引发剂可选自在宽带波长的UV曝光下,能释放出自由基以进行交联反应的有机物,例如苯乙酮类(Acetophenone)、安息香类(benzoin)、二苯甲酮类(benzophenone)、硫杂蒽酮类(Thioxanthone)、蒽醌类(anthraquinone)的光引发剂。该光引发剂的重量百分比为2-10wt%,以该官能基化大豆油化合物的重量为基准。
由于该涂布组合物是包含具有式(I)结构的官能基化大豆油化合物,使得该涂布组合物具有较大的粘性,非常适合以平板印刷、网版印刷方式形成于一基材之上。此外,为使该涂布组合物可以旋转涂布、或是喷涂方式形成于一基材之上,该涂布组合物可更包含一亚克力单体(例如具有至少两个末端亚克力官能基的亚克力单体),其中该亚克力单体的重量百分比为0.01-30wt%(该重量百分比是以该官能基化大豆油化合物的重量为基准)。
根据本发明一实施例,该涂布组合物可更包含一色料(例如染料(dye)或颜料(pigment)),因此该涂布组合物可作为一般涂料。其中,该色料的重量百分比为0.01-100wt%(该重量百分比是以该官能基化大豆油化合物的重量为基准)。
为使该具有式(I)结构的官能基化大豆油化合物的涂布组合物所形成涂膜不溶于水,但用碱水(例如5wt%的NaOH水溶液)能去除,使得被涂布的基材可重复再使用,该涂布组合物可更包含一具有如式(II)所示结构的官能基化大豆油化合物,
式(II)
其中,n’是各自独立的整数,介于1-10之间;m’是各自独立的整数,介于1-10之间;x’是各自独立的整数,为1或2;R8是各自独立的取代基,为羟基、其中i′为1或2,j’为介于4-60之间的整数,R9为氢、C1-3的烷基、或是丙烯基,R10及R11为氢,或者R10及R11连接在一起而与其所连接的碳原子共同形成一饱和或不饱和六元环,R12为氢、或C1-6的烷基。
由于具有式(II)所示结构的官能基化大豆油化合物并没有含羧酸基,因此通过该具有式(II)所示结构的官能基化大豆油化合物的加入,使得该涂布组合物中,该具有式(I)及式(II)结构的官能基化大豆油的羧酸基(-COOH)与该具有式(I)及式(II)结构的官能基化大豆油的摩尔比可被调整至0.1-0.5之间(或介于0.1-0.2之间),如此一来使得所形成涂膜,不溶于水,但可以碱水去除。
根据本发明一实施例,若在制备具有式(I)所示结构的官能基化大豆油化合物时,在一添加马来酐的步骤中减少马来酐的添加量(例如将马来酐的添加量调降至0.1-0.5当量,其中该大豆油的当量为1),所获得的官能基化大豆油化合物即为同时包含具有式(I)及式(II)所示结构的官能基化大豆油化合物的混合物,且该混合物所具有的羧酸基(-COOH)与大豆油的摩尔比也落在0.1-0.5的范围之间。
本发明也提供一种涂布组合物可作为消光涂料、防炫光涂料、扩散膜涂料、或是导光板油墨涂料。根据本发明其它实施例,该涂布组合物可包含一光引发剂;一无机氧化物颗粒;以及,具有式(I)结构的官能基化大豆油化合物。该光引发剂的重量百分比为2-10wt%,该无机氧化物颗粒的重量百分比为2-40wt%(该重量百分比以该官能基化大豆油化合物的重量为基准)。该无机氧化物颗粒为二氧化钛、或二氧化硅,且该无机氧化物颗粒的粒径可介于0.01-1.0μm之间。此外,如上所述,该涂布组合物也可包含一亚克力单体,其中该亚克力单体的重量百分比为0.01-30wt%。
为了让本发明的上述和其它目的、特征、和优点能更明显易懂,下文特举数实施例及比较实施例,来说明本发明所述的具有官能基化大豆油化合物、及包含其的涂布组合物。
官能基化大豆油化合物的制备
实施例1
首先,将75.0g PEO 750(poly(ethylene oxide)、分子量为750、0.1mole,由东联化学制造)与14.8g邻-苯二甲酐(Phthalic Anhydride、0.1mole、由Aldrich制造)加入250ml反应瓶中,再加入1.83g三苯基膦(triphenyl phosphine、2wt%、由Aldrich制造)作为催化剂,在95±3℃下反应2小时。
接着,加入100g环氧大豆油(0.1mole,长春石化),并加入0.05g对羟基苯甲醚(p-hydroxyanisole、0.4mmole,Aldrich,作为阻聚剂),在95±3℃下反应4小时。接着,加入丙烯酸14.4g(0.2mole,由Aldrich制造),并在95±3℃下反应6小时;接着,加入9.8g马来酐(0.1mole,由Aldrich制造)(马来酐与环氧大豆油的摩尔比为1),在95±3℃下反应2小时,最后得到官能基化大豆油化合物1。上述反应的反应式如下所示:
官能基化大豆油化合物1
利用核磁共振光谱来确认所得的官能基化大豆油化合物1结构,所得的光谱信息请参照图1;
利用凝胶渗透色谱(GPC)对官能基化大豆油化合物1进行分析,测得Mn约2800、Mw约3800、Mp约3100。
实施例2-10
以实施例1所述制备官能基化大豆油化合物1的步骤进行,除了分别将马来酐与环氧大豆油的摩尔比调降为0.05、0.1、0.2、0.3、0.4、0.5、0.6、0.7、及0.8,分别得到官能基化大豆油化合物的混合物1-9。由于马来酐与环氧大豆油的摩尔比小于1,因此该官能基化大豆油化合物的混合物1-9除了包含官能基化大豆油化合物1外,亦包含不具有羧酸基的官能基化大豆油化合物2:
涂布组合物的制备及性质测定
实施例11-14
将官能基化大豆油化合物的混合物1-4(2.04g)分别与光引发剂0.15g(商品编号为PI1173,由长兴化工制造贩卖)混合,得到涂布组合物1-4(即实施例11-14)。接着,以25μm刮刀将涂布组合物1-4涂布于亚克力基板上,并以100℃预烤5分钟。接着,进行UV曝光(365nm,1150mJ/cm2)硬化成膜,并进行溶解、附着度、硬度、及透光率测试,结果如表1所示:
表1
(备注:附着度测试的条件是使用透明胶带(3M,Scotch#600)紧密贴合于涂布组合物硬化层上,以垂直角度快速撕移胶带,以测试该硬化层是否未被破坏。)
由表1可知,当涂布组合物(包含官能基化大豆油化合物及光引发剂)的含羧酸基当量数介于0.1及0.2之间时,该涂布组合物所形成的硬化层,具有高的附着度及硬度,且不会溶于水但可以碱水移除。
实施例15-21
将官能基化大豆油化合物的混合物3-9(2.04g)分别与光引发剂0.15g(商品编号为PI1173,由长兴化工制造贩卖)、亚克力单体0.325g(商品编号EM235、pentaerythritol triacrylate,由长兴化工制造)、及1ml乙醇混合,得到涂布组合物5-11(即实施例15-21)。接着,以25μm刮刀将涂布组合物5-11涂布于亚克力基板上,并以100℃预烤5分钟。接着,进行UV曝光(365nm,1150mJ/cm2)硬化成膜,并进行溶解测试,结果如表2所示:
表2
由表2可知,当涂布组合物更进一步包含一亚克力单体,且羧酸基当量数介于0.3-0.5时,该涂布组合物所形成的硬化层,不会溶于水且可以碱水移除。
实施例22-24
依照表3将0.12g二氧化硅(粒径为20nm)、0.24g二氧化硅(粒径为20nm)、及0.12g二氧化钛(粒径为0.3μm)分别与官能基化大豆油化合物的混合物4(2.04g)、光引发剂0.15g(商品编号为PI1173,由长兴化工制造贩卖)、亚克力单体0.325g(商品编号EM235、pentaerythritol triacrylate,由长兴化工制造)、及1ml乙醇混合,得到涂布组合物12-14(即实施例22-24)。接着,以25μm刮刀将涂布组合物12-14涂布于亚克力基板上,并以100℃预烤5分钟。接着,进行UV曝光(365nm,1150mJ/cm2)硬化成膜,并进行透光率、光泽度、及雾度测试,结果如表3所示:
表3
由表3可知,当涂布组合物更进一步包含一亚克力单体及一无机氧化物时,该涂布组合物适合作为消光涂料、防炫光涂料、或是扩散膜涂料。
实施例25-26
将官能基化大豆油化合物的混合物3、及6(2.04g)分别与光引发剂0.15g(商品编号为PI1173,由长兴化工制造贩卖)混合,得到涂布组合物15及16(即实施例25-26)。接着,以25μm刮刀将涂布组合物15及16涂布于亚克力基板上,并以100℃预烤5分钟。接着,进行UV曝光(365nm,1150mJ/cm2)硬化成膜,并进行溶解、及附着力测试,结果如表4所示。
比较实施例1-3
将0.2,0.5与1.0当量的甲基丙烯酸(由Aldrich制造)分别与1当量的环氧大豆油亚克力寡聚物(商品编号6261、由长兴化工制造。该环氧大豆油亚克力寡聚物不包含羧酸基与PEO链段)、以及光引发剂(0.15g、PI 1173/长兴化工),得到涂布组合物17-19(即比较实施例1-3)。接着,以25μm刮刀将涂布组合物17-19涂布于亚克力基板上,并以100℃预烤5分钟。接着,进行UV曝光(365nm,1150mJ/cm2)硬化成膜,并进行溶解、及附着力测试,结果如表4所示。
表4
由表4可知,由环氧大豆油亚克力寡聚物与甲基丙烯酸混合所得的涂布组合物(比较实施例1-3),经硬化所得的膜层,是同时可溶于水及碱水,或是同时皆不溶于水及碱水,无法通过碱可溶水不溶的测试条件。
本发明所述的官能基化大豆油化合物,是将一环氧大豆油上的环氧基开环,并导入长链氧烷基、羧酸基、以及亚克力基所得。长链氧烷基的导入可是增加化合物的亲水性以及对基材的附着度;羧酸基的导入是增加化合物的碱水可溶性;亚克力基团的导入可使化合物具有可进行光硬化的能力。此外,本发明所述的包含该官能基化大豆油化合物的涂布组合物,可进一步通过控制羧酸基的含量来达到同时具有耐水性、却可以碱水去除的特性,以使得被涂布的基材可回收再利用。再者,本发明所述涂布组合物,可更进一添加无机氧化物粒子,以应用在消光涂料、防炫光涂料、或是扩散膜涂料上。
虽然本发明已以数个较佳实施例揭露如上,然其并非用以限定本发明,任何所属技术领域中具有通常知识者,在不脱离本发明的精神和范围内,当可作任意的更动与润饰,因此本发明的保护范围当视后附的权利要求书所界定的范围为准。
Claims (23)
1.一种官能基化大豆油化合物,其具有如式(I)所示结构:
其中,n是各自独立的整数,介于1-10之间;m是各自独立的整数,介于1-10之间;x是各自独立的整数,为1或2;R1是各自独立的取代基,为羟基、或其中i为1或2,j为介于4-60之间的整数,R2为氢、C1-3的烷基、或是丙烯基,R3及R4为氢,或者R3及R4连接在一起而与其所连接的碳原子共同形成一饱和或不饱和六元环,R5、R6、及R7是各自独立的取代基,且为氢、或C1-6的烷基,
其中式(I)所示结构中仅有一R1为至少一R1为至少一R1为
2.如权利要求1所述的官能基化大豆油化合物,其中式(I)所示结构中仅有一R1为至少一R1为而其它R1为其中R2为氢、C1-3的烷基、或是丙烯基、j为介于4-60之间的整数。
3.如权利要求1所述的官能基化大豆油化合物,其中式(I)所示结构中仅有一R1为至少一R1为而其它R1为其中R2为氢、C1-3的烷基、或是丙烯基、j为介于4-60之间的整数。
4.如权利要求1所述的官能基化大豆油化合物,其中式(I)所示结构中仅有一R1为至少一R1为而其它R1皆为其中i为1或2,j为介于4-60之间的整数,R2为氢、C1-3的烷基、或是丙烯基,R3及R4为氢,或者R3及R4连接在一起而与其所连接的碳原子共同形成一饱和或不饱和六元环,R5、R6、及R7是各自独立的取代基,且为氢、或C1-6的烷基。
5.如权利要求1所述的官能基化大豆油化合物,其中R5、R6、及R7是各自独立的取代基,且为氢、甲基、乙基、丙基、异丙基、丁基、异丁基、戊基、或己基。
6.如权利要求1所述的官能基化大豆油化合物,其中R3及R4连接在一起而与其所连接的碳原子共同形成一苯基或吡啶基。
7.一种涂布组合物,包含:
一光引发剂;以及
如权利要求1所述的具有式(I)结构的官能基化大豆油化合物。
8.如权利要求7所述的涂布组合物,其中该光引发剂的重量百分比为2-10wt%,以该官能基化大豆油化合物的重量为基准。
9.如权利要求7所述的涂布组合物,更包含一亚克力单体,其中该亚克力单体具有至少两个末端亚克力官能基。
10.如权利要求9所述的涂布组合物,其中该亚克力单体的重量百分比为0.01-30wt%,以该官能基化大豆油化合物的重量为基准。
11.如权利要求7所述的涂布组合物,更包含一色料,其中该色料为染料或颜料。
12.如权利要求11所述的涂布组合物,其中该色料的重量百分比为0.01-100wt%,以该官能基化大豆油化合物的重量为基准。
13.如权利要求7所述的涂布组合物,更包含:
一具有如式(II)所示结构的官能基化大豆油化合物,
其中,n’是各自独立的整数,介于1-10之间;m’是各自独立的整数,介于1-10之间;x’是各自独立的整数,为1或2;R8是各自独立的取代基,为羟基、或其中i'为1或2,j’为介于4-60之间的整数,R9为氢、C1-3的烷基、或是丙烯基,R10及R11为氢,或者R10及R11连接在一起而与其所连接的碳原子共同形成一饱和或不饱和六元环,R12为氢、或C1-6的烷基。
14.如权利要求13所述的涂布组合物,其中该具有式(I)结构的官能基化大豆油的羧酸基与该具有式(I)及式(II)结构的官能基化大豆油摩尔比介于0.1-0.5之间。
15.如权利要求7所述的涂布组合物,更包含一无机氧化物颗粒,其中该无机氧化物颗粒为二氧化钛、或二氧化硅。
16.如权利要求15所述的涂布组合物,其中该无机氧化物颗粒的粒径介于0.01-1.0μm之间。
17.如权利要求15所述的涂布组合物,其中该无机氧化物颗粒的重量百分比为2-40wt%,以该官能基化大豆油化合物的重量为基准。
18.一种涂布组合物,包含:
一光引发剂;
一无机氧化物颗粒;以及
如权利要求1所述的具有式(I)结构的官能基化大豆油化合物。
19.如权利要求18所述的涂布组合物,其中该无机氧化物颗粒为二氧化钛或二氧化硅。
20.如权利要求18所述的涂布组合物,其中该无机氧化物颗粒的粒径介于0.01-1.0μm之间。
21.如权利要求18所述的涂布组合物,其中该光引发剂的重量百分比为2-10wt%,该无机氧化物颗粒的重量百分比为2-40wt%,以该官能基化大豆油化合物的重量为基准。
22.如权利要求18所述的涂布组合物,更包含一亚克力单体,其中该亚克力单体具有至少两个末端亚克力官能基。
23.如权利要求22所述的涂布组合物,其中该亚克力单体的重量百分比为0.01-30wt%,以该官能基化大豆油化合物的重量为基准。
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