功能材料
功能材料
공능재료
JOURNAL OF FUNCTIONAL MATERIALS
2014年
16期
16090-16095
,共6页
王海花%李凯斌%沈一丁%费贵强%柯勇
王海花%李凱斌%瀋一丁%費貴彊%柯勇
왕해화%리개빈%침일정%비귀강%가용
甲基丙烯酸缩水甘油酯%甲基丙烯酰氧乙基三甲基氯化铵%聚乙烯醇纤维%阳离子%反应活性
甲基丙烯痠縮水甘油酯%甲基丙烯酰氧乙基三甲基氯化銨%聚乙烯醇纖維%暘離子%反應活性
갑기병희산축수감유지%갑기병희선양을기삼갑기록화안%취을희순섬유%양리자%반응활성
glycidyl methacrylate%methacryloyloxy ethyl trimethyl ammonium chloride%PVA fiber%cationic%reac-tion activity
通过多元悬浮接枝共聚法,以硝酸铈铵(CAN)为引发剂、甲基丙烯酰氧乙基三甲基氯化铵(DMC)和甲基丙烯酸缩水甘油酯(GMA)为功能化单体,制备了一种具有反应活性的阳离子型改性聚乙烯醇(PVA)纤维。讨论了 DMC 和 GMA 添加量、CAN浓度、H+浓度等对 PVA 纤维接枝率的影响,以及DMC和GMA添加量对纸张强度的影响。结果表明,当 DMC 与 GMA 质量比为2∶3、CAN 浓度为8×10-3 mol/L、H+浓度为0.1 mol/L 时,纤维的接枝率为15.6%,此时纸张获得较佳强度,耐折度为241次,干拉力、湿拉力可分别达到83.10,30.40 N,湿强度为36.58%。FT-IR和X射线能谱证实了GMA和DMC在PVA纤维表面发生接枝共聚反应。扫描电镜表明,当DMC与GMA质量比为2∶3时,改性PVA纤维表面形成了沿纤维纵向排列的不规则突起。
通過多元懸浮接枝共聚法,以硝痠鈰銨(CAN)為引髮劑、甲基丙烯酰氧乙基三甲基氯化銨(DMC)和甲基丙烯痠縮水甘油酯(GMA)為功能化單體,製備瞭一種具有反應活性的暘離子型改性聚乙烯醇(PVA)纖維。討論瞭 DMC 和 GMA 添加量、CAN濃度、H+濃度等對 PVA 纖維接枝率的影響,以及DMC和GMA添加量對紙張彊度的影響。結果錶明,噹 DMC 與 GMA 質量比為2∶3、CAN 濃度為8×10-3 mol/L、H+濃度為0.1 mol/L 時,纖維的接枝率為15.6%,此時紙張穫得較佳彊度,耐摺度為241次,榦拉力、濕拉力可分彆達到83.10,30.40 N,濕彊度為36.58%。FT-IR和X射線能譜證實瞭GMA和DMC在PVA纖維錶麵髮生接枝共聚反應。掃描電鏡錶明,噹DMC與GMA質量比為2∶3時,改性PVA纖維錶麵形成瞭沿纖維縱嚮排列的不規則突起。
통과다원현부접지공취법,이초산시안(CAN)위인발제、갑기병희선양을기삼갑기록화안(DMC)화갑기병희산축수감유지(GMA)위공능화단체,제비료일충구유반응활성적양리자형개성취을희순(PVA)섬유。토론료 DMC 화 GMA 첨가량、CAN농도、H+농도등대 PVA 섬유접지솔적영향,이급DMC화GMA첨가량대지장강도적영향。결과표명,당 DMC 여 GMA 질량비위2∶3、CAN 농도위8×10-3 mol/L、H+농도위0.1 mol/L 시,섬유적접지솔위15.6%,차시지장획득교가강도,내절도위241차,간랍력、습랍력가분별체도83.10,30.40 N,습강도위36.58%。FT-IR화X사선능보증실료GMA화DMC재PVA섬유표면발생접지공취반응。소묘전경표명,당DMC여GMA질량비위2∶3시,개성PVA섬유표면형성료연섬유종향배렬적불규칙돌기。
Cationic polyvinyl alcohol (PVA)fibers with reaction activity were synthesized via suspension graft-ing multi-copolymerization using methacryloyloxy ethyl trimethyl ammonium chloride (DMC)and glycidyl methacrylate (GMA)as functional monomers.The influence of DMC and GMA content,concentration of CAN and H+ on grafting rate (GR)of PVA fiber together with the influence of DMC and GMA content on paper strength was discussed.The results show that the desired condition for a better strength of paper was as fol-low:m(DMC)was 2 g,the concentration of CAN and H+ was 8×10-3 mol/L and 0.1 mol/L respectively.At this time,GR was 15.6%,folding endurance was 241 times,dry tensile strength was 83.10 N,wet tensile strength was 30.40 N,wet strength was 36.58%.FT-IR and X-ray energy spectrum (EDX)indicate that the grafting copolymerization of GMA and DMC took place on the surface of PVA fiber.SEM photographs show that when m(DMC)/m(GMA)was 2∶3 ,it formed irregular protrusions arranged longitudinally on the surface of modified PVA fiber.