噴墨打印陽離子丙烯酸酯乳液的制備
本文選題:陽離子丙烯酸酯乳液 + 季銨鹽乳化劑 ; 參考:《南京林業(yè)大學(xué)》2016年碩士論文
【摘要】:本文設(shè)計合成了甲基丙烯酸二甲氨基乙酯類和丙烯酰胺類陽離子乳化劑,并合成相應(yīng)的陽離子乳液,然后將其應(yīng)用于噴墨打印中,并通過加入交聯(lián)體系和功能單體提高乳液的耐水性和穩(wěn)定性。同時研究合成新型的馬來酸系可聚合乳化劑,主要研究內(nèi)容如下:(1)以甲基丙烯酸二甲氨基乙酯為單體,制備季銨鹽型高分子乳化劑,將其與十六烷基三甲基溴化銨復(fù)配使用,再與苯乙烯和丙烯酸丁酯單體共聚,制備了陽離子丙烯酸酯乳液。實驗結(jié)果表明:當(dāng)高分子陽離子乳化劑與十六烷基三甲基溴化銨的質(zhì)量比為34.6:0.6時,得到的陽離子乳液最穩(wěn)定。并通過加入不同的交聯(lián)體系探討其對高分子陽離子乳液的耐水性與粒徑的影響,同時用紅外光譜,差示掃描量熱儀、激光粒度分布儀對制得的乳液進(jìn)行表征。實驗結(jié)果表明:加入功能單體三甘醇二甲基丙烯酸酯類交聯(lián)劑(V-389)時乳液的耐水性最好,當(dāng)V-389用量為1.7%(占主單體總量)時,乳液的吸水率達(dá)到最小值3.62%,性能較優(yōu)良。(2)以丙烯酰胺為主單體,十六烷基三甲基溴化銨為相轉(zhuǎn)移催化劑,合成了高分子陽離子乳化劑,再與苯乙烯和丙烯酸丁酯單體共聚,制備了陽離子丙烯酸酯乳液。實驗結(jié)果表明:當(dāng)十六烷基三甲基溴化銨用量為1.0 g,丙烯酰胺用量為5.0 g,環(huán)氧氯丙烷用量為5.2 g時,所得到的乳化劑的乳化性能最優(yōu)良。在制備陽離子乳液過程中,加入不同的交聯(lián)體系來探討其對耐水性和粒徑的影響,同時用紅外光譜,差示熱掃描儀、激光粒度分布儀對制得的乳液進(jìn)行表征。結(jié)果表明:當(dāng)加入交聯(lián)體系雙丙酮丙烯酰胺-己二酰肼基交聯(lián)體系為1.0 g時,吸水率達(dá)到最低值5.39%。(3)用自制的甲基丙烯酸二甲氨基乙酯系高分子乳化劑制備了噴墨用陽離子聚丙烯酸酯乳液。并利用透射電子顯微鏡、差熱示掃描儀、粒徑分析儀對制得的聚合物乳液的結(jié)構(gòu)進(jìn)行了表征,探討了聚合物在噴墨打印中的油墨吸收性。結(jié)果表明:采用核殼乳液聚合法,功能單體羥甲基丙烯酰胺為4.60%(占主單體總量,下同),烯丙基三甲氧基硅烷量為2.30%,DM為19%,納米三氧化二鋁分散液為10.67%(占乳液總量),此時合成的乳液的吸墨性能最好,打出的圖片最清晰。(4)將制得的丙烯酰胺類陽離子乳液與三氧化二鋁配合使用,并應(yīng)用于圖像打印中,打印的圖像較為清晰,同時利用透射電子顯微鏡對此乳液結(jié)構(gòu)進(jìn)行了表征。(5)以馬來酸酐和N,N-二甲基乙醇胺為反應(yīng)物,對甲苯磺酸鈉為催化劑,合成了馬來酸二乙醇胺酯,馬來酸二乙醇胺酯再與氯乙酸鈉進(jìn)行季銨化反應(yīng),合成了一種新型的可聚合型的馬來酸系陽離子單體。并用混合指示劑兩相滴定法測定反應(yīng)轉(zhuǎn)化率,同時用紅外光譜和核磁共振氫譜對產(chǎn)物結(jié)構(gòu)進(jìn)行了分析。正交實驗結(jié)果表明:馬來酸二乙醇胺酯與氯乙酸鈉的摩爾比為1:1.2,反應(yīng)時間為6 h,反應(yīng)溫度為70℃,此時叔胺轉(zhuǎn)化率最高可達(dá)76.17%。用上述自制的單體制備陽離子乳化劑,并將其用于乳液聚合,制備出較穩(wěn)定的陽離子乳液。
[Abstract]:Methyl two dimethylamino ethyl methacrylate and acrylamide cationic emulsifier has been synthesized, and the synthesis of cationic emulsion, and then applied to inkjet printing, and the addition of crosslinking system and functional monomer emulsion to improve water resistance and stability. At the same time on the synthesis of maleic acid, emulsifier, main the research contents are as follows: (1) to two dimethylamino ethyl methacrylate as monomer, preparation of quaternary ammonium salt type polymer emulsifier, its use with sixteen alkyl three methyl bromide combined with styrene and butyl acrylate monomers, cationic acrylic emulsion has been prepared. The experimental results show that when the cationic polymer emulsifier and sixteen alkyl three methyl bromide mass ratio was 34.6:0.6, the most stable cationic emulsion. By adding different crosslinking systems on polymer Effect of cationic emulsion resistance and particle size, at the same time by infrared spectroscopy, differential scanning calorimetry, laser particle size analyzer were used to characterize the prepared emulsion. The experiment results show that adding functional monomer three glycol two methyl acrylate (V-389) emulsion crosslinking agent when the water resistance when the best. The amount of V-389 was 1.7% (for total monomer), emulsion water absorption rate reaches a minimum value of 3.62%, a good performance. (2) using acrylamide as main monomers, sixteen alkyl three methyl ammonium bromide as phase transfer catalyst, polymer cationic emulsifier was synthesized with styrene and butyl acrylate monomers, cationic acrylic emulsion has been prepared. The experimental results show that when sixteen alkyl three methyl bromide dosage is 1 g, dosage of acrylamide was 5 g, epichlorohydrin dosage is 5.2 g, the most excellent emulsifier emulsion in the preparation of cation. In the process of seed emulsion, adding different crosslinking systems to explore its impact on the water resistance and particle size, at the same time by infrared spectroscopy, differential scanning calorimetry, laser particle size analyzer were used to characterize the prepared emulsion. The results show that: when adding diacetone acrylamide - crosslinking system has two hydrazide radical crosslinking system was 1 g, water absorption rate reaches a minimum value (3 5.39%.) with two dimethylamino ethyl methacrylate polymer emulsifier were prepared by cationic polyacrylate emulsion and inkjet. Using transmission electron microscopy, differential thermal scanner shows, particle size analysis structure of polymer emulsion prepared by the instrument were characterized on ink absorbent polymers in ink-jet printing. The results show that the polymerization using core-shell emulsion, functional monomer N-hydroxymethyl acrylamide was 4.60% (for total monomer, the same below), allyltrimethoxysilane weight is 2.30%, DM 19%, three nm two aluminum oxide dispersion was 10.67% (accounting for total, the emulsion) ink receptity emulsion is best, play the picture most clearly. (4) the prepared acrylamide cationic emulsion and three with the use of two aluminum oxide, and applied to the image printing, print the image is clearly, at the same time using transmission electron microscopy in the emulsion was characterized. (5) with maleic anhydride and N, N- two methyl diethanolamine as reactants and sodium p-toluene sulfonate as catalyst, maleic acid two ethanol amine ester was synthesized with maleic acid two ethanol amine ester and then quaternization reaction with sodium chloroacetate. A new type of polymerizable maleic acid cationic monomers were synthesized. Using mixed indicator two-phase titration method for the determination of the conversion rate, at the same time by infrared spectroscopy and nuclear magnetic resonance spectroscopy on the structure of the product was analyzed. The experimental results show that maleic acid The molar ratio of two ethanolamine to sodium chloroacetate is 1:1.2, the reaction time is 6 h, and the reaction temperature is 70 degrees. The conversion rate of tertiary amine is up to 76.17%. at the same time. The cationic emulsifier made by the above homemade single system is applied to emulsion polymerization, and a stable cationic emulsion is prepared.
【學(xué)位授予單位】:南京林業(yè)大學(xué)
【學(xué)位級別】:碩士
【學(xué)位授予年份】:2016
【分類號】:TQ316.33;O648.23
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