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相转移催化法合成十二烷基缩水甘油醚 总被引:1,自引:0,他引:1
以十二醇和二氯丙醇为原料,用相转移催化剂直接合成了十二烷基缩水甘油醚。考察了催化剂种类、原料摩尔比、反应时间和反应温度对十二烷基缩水甘油醚收率的影响。结果表明,以四丁基溴化铵为催化剂,甲苯为溶剂,n(十二醇)∶n(二氯丙醇)=1∶1.60,反应温度50℃,反应时间4 h,十二烷基缩水甘油醚收率可达73.2%。用IR、1HNMR对产物结构进行了表征,采用测定产品环氧值的方法来计算十二烷基缩水甘油醚的收率。 相似文献
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摘 要:以玉米淀粉为原料,丁基缩水甘油醚为疏水化试剂,氢氧化钠作为催化剂,水作为溶剂,在较温和反应条件下合成了2-羟基-3-丁氧基丙基淀粉(HBPS)。通过考察反应温度、反应时间、碱用量、水用量等因素对取代度和反应效率的影响,确定的最佳的制备条件为:当n(BGE):n(AGU)=0.615时,水用量m(H2O):m(AGU)=2:1、碱用量n(NaOH):n(AGU)=0.5:1、反应温度75℃和反应时间为5h,产品取代度MS=0.45,反应效率为RE=73%。使用IR、1H-NMR、13C-NMR对产物结构进行了表征,证明结构的正确。热重实验表明,疏水基团的引入可提高淀粉的耐热性能。 相似文献
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以玉米淀粉为原料,丁基缩水甘油醚(BGE)为疏水化试剂,氢氧化钠作催化剂,水为溶剂,在较温和反应条件下合成了2-羟基-3-丁氧基丙基淀粉(HBPS)。考察了反应温度、反应时间、碱用量、水用量和BGE用量等因素对取代度和反应效率的影响,确定了最佳制备条件为:当n(BGE)/n〔淀粉葡萄糖单元(AGU)〕=0.615,m(H2O)∶m(AGU)=2∶1,n(NaOH)∶n(AGU)=0.5∶1,反应温度75℃和反应时间为5h,产品取代度MS=0.45,反应效率RE=73%。用IR、1HNMR、13CNMR对产物结构进行了表征。热重实验表明,疏水基团的引入可提高淀粉的耐热性能。 相似文献
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1,2-环己二醇二缩水甘油醚的合成及应用 总被引:1,自引:0,他引:1
1,2-环己二醇二缩水甘油醚是一种重要的化工产品,通过实验研究,优化了1,2-环己二醇二缩水甘油醚的合成条件,得到了新的最佳合成工艺方案:n(1,2-环己二醇)/n(环氧氯丙烷)=1/2.4;醚化反应温度为60~65℃;环氧化反应温度为35~40℃;最后介绍了1,2-环己二醇二缩水甘油醚的应用。 相似文献
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《应用化工》2016,(11)
以对氯苄醇、3-溴丙炔为起始原料,经过醚化反应合成中间产物1-氯-4-((丙-2-炔-1-基氧基)甲基)苯,再与多聚甲醛、三乙胺经曼尼希反应,合成具有抗心律不齐功能的化合物4-((4-氯苄基)氧基)-N,N-二乙基丁-2-炔-1-胺。通过GC-MS和1H NMR表征了产物结构。确定合成4-((4-氯苄基)氧基)-N,N-二乙基丁-2-炔-1-胺的较优条件为:1-氯-4-((丙-2-炔-1-基氧基)甲基)苯1 mmol,n(1-氯-4-((丙-2-炔-1-基氧基)甲基)苯)∶n(多聚甲醛)∶n(三乙胺)=1∶1∶2,溶剂为二氧六环,催化剂为氯化亚铜,其用量占原料质量的20%,反应温度90℃,反应时间6 h,在上述适宜条件下4-((4-氯苄基)氧基)-N,N-二乙基丁-2-炔-1-胺的得率为74.6%。 相似文献
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《应用化工》2022,(11)
以对氯苄醇、3-溴丙炔为起始原料,经过醚化反应合成中间产物1-氯-4-((丙-2-炔-1-基氧基)甲基)苯,再与多聚甲醛、三乙胺经曼尼希反应,合成具有抗心律不齐功能的化合物4-((4-氯苄基)氧基)-N,N-二乙基丁-2-炔-1-胺。通过GC-MS和1H NMR表征了产物结构。确定合成4-((4-氯苄基)氧基)-N,N-二乙基丁-2-炔-1-胺的较优条件为:1-氯-4-((丙-2-炔-1-基氧基)甲基)苯1 mmol,n(1-氯-4-((丙-2-炔-1-基氧基)甲基)苯)∶n(多聚甲醛)∶n(三乙胺)=1∶1∶2,溶剂为二氧六环,催化剂为氯化亚铜,其用量占原料质量的20%,反应温度90℃,反应时间6 h,在上述适宜条件下4-((4-氯苄基)氧基)-N,N-二乙基丁-2-炔-1-胺的得率为74.6%。 相似文献
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M. S. J. Simmonds W. M. Blaney F. Delle Monache M. Marquina Mac-Quhae G. B. Marini Bettolo 《Journal of chemical ecology》1985,11(12):1593-1599
Vismiones and ferruginins, representatives of a new class of lypophilic anthranoids from the genusVismia were found to inhibit feeding in larvae of species ofSpodoptera, Heliothis, and inLocusta migratoria. 相似文献
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Cheng-Le Zhao Shane Porzio Alan Smith Haiyan Ge H. T. Davis L. E. Scriven 《Journal of Coatings Technology and Research》2006,3(2):109-115
Despite its industrial importance, the subject of freeze-thaw (F/T) stability of latex coatings has not been studied extensively.
There is also a lack of fundamental understanding about the process and the mechanisms through which a coating becomes destabilized.
High pressure (2100 bar) freezing fixes the state of water-suspended particles of polymer binder and inorganic pigments without
the growth of ice crystals during freezing that produce artifacts in direct imaging scanning electron microscopy (SEM) of
fracture surfaces of frozen coatings. We show that by incorporating copolymerizable functional monomers, it is possible to
achieve F/T stability in polymer latexes and in low-VOC paints, as judged by the microstructures revealed by the cryogenic
SEM technique. Particle coalescence as well as pigment segregation in F/T unstable systems are visualized. In order to achieve
F/T stability in paints, latex particles must not flocculate and should provide protection to inorganic pigment and extender
particles. Because of the unique capabilities of the cryogenic SEM, we are able to separate the effects of freezing and thawing,
and study the influence of the rate of freezing and thawing on F/T stability. Destabilization can be caused by either freezing
or thawing. A slow freezing process is more detrimental to F/T stability than a fast freezing process; the latter actually
preserves suspension stability during freezing.
Presented at the 82nd Annual Meeting of the Federation of Societies for Coatings Technology, October 27–29, 2004 in Chicago,
IL. Tied for first place in The John A. Gordon Best Paper Competition. 相似文献
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Ethanol and (−)-α-Pinene: Attractant Kairomones for Bark and Ambrosia Beetles in the Southeastern US
In 2002–2004, we examined the flight responses of 49 species of native and exotic bark and ambrosia beetles (Coleoptera: Scolytidae
and Platypodidae) to traps baited with ethanol and/or (−)-α-pinene in the southeastern US. Eight field trials were conducted
in mature pine stands in Alabama, Florida, Georgia, North Carolina, and South Carolina. Funnel traps baited with ethanol lures
(release rate, about 0.6 g/day at 25–28°C) were attractive to ten species of ambrosia beetles (Ambrosiodmus tachygraphus, Anisandrus sayi, Dryoxylon onoharaensum, Monarthrum mali, Xyleborinus saxesenii, Xyleborus affinis, Xyleborus ferrugineus, Xylosandrus compactus, Xylosandrus crassiusculus, and Xylosandrus germanus) and two species of bark beetles (Cryptocarenus heveae and Hypothenemus sp.). Traps baited with (−)-α-pinene lures (release rate, 2–6 g/day at 25–28°C) were attractive to five bark beetle species
(Dendroctonus terebrans, Hylastes porculus, Hylastes salebrosus, Hylastes tenuis, and Ips grandicollis) and one platypodid ambrosia beetle species (Myoplatypus flavicornis). Ethanol enhanced responses of some species (Xyleborus pubescens, H. porculus, H. salebrosus, H. tenuis, and Pityophthorus cariniceps) to traps baited with (−)-α-pinene in some locations. (−)-α-Pinene interrupted the response of some ambrosia beetle species
to traps baited with ethanol, but only the response of D. onoharaensum was interrupted consistently at most locations. Of 23 species of ambrosia beetles captured in our field trials, nine were
exotic and accounted for 70–97% of total catches of ambrosia beetles. Our results provide support for the continued use of
separate traps baited with ethanol alone and ethanol with (−)-α-pinene to detect and monitor common bark and ambrosia beetles
from the southeastern region of the US. 相似文献
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Peter A. Edwards Grant Striemer Dean C. Webster 《Journal of Coatings Technology and Research》2005,2(7):517-527
Glycidyl carbamate chemistry combines the excellent properties of polyurethanes with the crosslinking chemistry of epoxy resins.
Glycidyl carbamate functional oligomers were synthesized by the reaction of polyfunctional isocyanate oligomers and glycidol.
The oligomers were formulated into coatings with several amine functional crosslinkers at varying stoichiometric ratios and
cured at different temperatures. Properties such as solvent resistance, hardness, and impact resistance were dependent on
the composition and cure conditions. Most coatings had an excellent combination of properties. Studies were carried out to
determine the kinetics of the curing reaction of the glycidyl carbamate functional oligomers with multifunctional and model
amines. Detailed kinetic analysis of the curing reactions was also undertaken. The results indicated that the glycidyl carbamate
functional group is more reactive than a glycidyl ether group.
Presented at the 82nd Annual Meeting of the Federation of Societies for Coatings Technology, on October 27–29, 2004, in Chicago,
IL. 相似文献
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Dongjiang Yang Yao Xu Lei Zhang Shangru Zhai Dong Wu Yuhan Sun 《Journal of Coatings Technology and Research》2006,3(2):127-131
A highly moisture-proof polysilsesquioxane coating was obtained from a new bis-silylated precursor, which was synthesized from 3-aminopropyltriethoxysilane (APTES) and m-xylylene diisocyanate (m-XDI) in tetrahydrofuran (THF) and verified by 1H MAS NMR. For direct comparison purposes, an SiO2 coating was also prepared by the Stöber method using tetraethoxysilane (TEOS) as the reactant. Interestingly, the coating obtained from the polysilsesquioxane sol exhibited a much higher moisture resistance capability than its counterpart, which was attributed to its more compact feature between nanoparticles as characterized by N2 absorption experiment and transmission electron microscopy (TEM). Furthermore, its high transparency of about 92% showed potential for application in the protection of optical crystals. 相似文献