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    2019年, 第49卷, 第2期 刊出日期:2019-02-22 上一期    下一期
    基础研究
    可分解香兰素基非离子表面活性剂的乳化性
    The emulsibility of cleavable vanillin-based nonionic surfactants
    丁凤美,周翔,李居龙,邢志奇
    2019 (2):  63-69.  doi: 10.3969/j.issn.1001-1803.2019.02.001
    摘要 ( 374 )   HTML ( 88 )   PDF(1350KB) ( 438 )  

    针对已合成的含缩醛结构的环保型非离子表面活性剂香兰素辛二醇缩醛聚氧乙烯醚(VAEO),研究不同乙氧基链长的VAEOnn=6~24)的表面活性及乳化性,并与壬基酚聚氧乙烯醚(NPEO10)的表面活性及乳化性作比较。结果表明,随EO聚合度(n)增大,VAEOn降低表面张力和油/水界面张力的能力下降,对石蜡乳化能力减弱。EO聚合度为6~10的VAEOn与NPEO10降低表面张力的能力相近,乳化性能也相当。VAEOn降低油/水界面张力的能力较NPEO10差。采用Material Studio软件模拟分析VAEOn和NPEO10乳化石蜡的能力,结果表明VAEOn乙氧基链越长,乳化石蜡重新聚集的速度越快,即乳化性能越差,模拟结果与乳化石蜡分相法的实验结果相吻合。

    A series of environment-friendly nonionic surfactants, vanillin 1,2-octanediolacetal polyoxyethylene ethers (VAEO) with acetal structure, have been successfully synthesized previously. The surface activity and emulsibility of VAEOnn=6-24) were studied, which were also compared with that of nonylphenol polyoxyethylene ether (NPEO10). The results show that, as the polyoxyethylene chain length (n) of VAEOn increased, the abilities of VAEOn to reduce the surface tension/interfacial tension and to emulsify paraffin are both decreased. As for the VAEOn with low degree of EO polymerization (n=6-10), their surface activity and emulsibility are similar to those of NPEO10. The ability of VAEOn to reduce oil-water interfacial tension is worse than that of NPEO10. The software "Material Studio" is used to simulate VAEOn and NPEO10 in emulsifying paraffin in water, showing that the paraffin aggregated faster for the VAEOn with longer polyoxyethylene chain length, which is consistent with the experimental results by split-phase method.

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    科技讲座
    弱相互作用调控表面活性剂自组装(II)——表面活性剂的结构与设计
    Self-assembly of surfactants controlled by weak interactions(II)The structure and design of surfactants
    孙冠男,郑利强,孙继超
    2019 (2):  70-75.  doi: 10.3969/j.issn.1001-1803.2019.02.002
    摘要 ( 379 )   HTML ( 9 )   PDF(1099KB) ( 586 )  

    介绍了表面活性剂的结构、性质以及分类,综述了阴离子表面活性剂、阳离子表面活性剂、两性离子表面活性剂、非离子表面活性剂的分子间弱相互作用。另外,简述了低聚型表面活性剂和其他新型表面活性剂的结构及应用。

    The structure, properties and classification of surfactants are introduced. The weak interactions between molecules of anionic surfactants, cationic surfactants, zwitterionic surfactants and nonionic surfactants have been reviewed. The structure and application of oligomeric surfactants and other new types of surfactants are briefly introduced.

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    开发与应用
    马来酸酯磺酸盐型活性聚合物的合成及性能研究
    Synthesis and solution properties of polymeric sulfomaleate surfactants
    许格,郑延成,元平南,郑恒
    2019 (2):  76-82.  doi: 10.3969/j.issn.1001-1803.2019.02.003
    摘要 ( 375 )   HTML ( 7 )   PDF(1399KB) ( 435 )  

    根据分子结构与性能的关系,用马来酸酐(MA)、聚乙二醇(PEG)、辛醇合成了活性单体(MOPn),再与2-丙烯酰胺基-2-甲基丙磺酸(AMPS)、丙烯酰胺(AM)通过自由基胶束共聚法合成含有-SO3 -、-CONH2、EO醚等极性基团的二元和三元活性聚合物,并对其结构进行红外表征和热重分析。评价了聚合物在蒸馏水和无机盐介质中的表面性能,讨论了影响溶液表面活性的各因素以及单体摩尔比对其性质的影响。结果表明:合成的二元聚合物(PMOPnS)具有较好的水溶性和表面活性,活性单体MOP1000与AMPS摩尔比为1∶2的二元聚合物比1∶4的二元聚合物的表面活性更强。三元聚合物在高于258 ℃下开始分解。考察了三元聚合物单体摩尔比、无机盐质量浓度对聚合物黏度的影响。n(MOP1000)∶n(AMPS)∶n(AM)=0.5∶1∶98.5的三元聚合物PMOPSA-1具有较好的增黏效果和表/界面活性,2%三元聚合物PMOPSA-1在蒸馏水和2%NaCl介质中30 ℃黏度分别为1 108和1 157 mPa·s,在2%NaCl和0.1%CaCl2混合盐水中30 ℃表面张力和45 ℃下与煤油的界面张力分别为30.43和2.09 mN/m,表明合成的活性型聚合物具有较好的热稳定性、稠化性能和表/界面活性。

    Based on the relationship between the molecular structure and the properties of polymers, maleic anhydride (MA) , polyethylene glycol (PEG) and octanol were used as main raw materials to synthesize active monomers (MOPn) . The active monomers then reacted with 2-acrylamido-2-methylpropane sulfonic acid (AMPS) and acrylamide (AM) to obtain binary and ternary polymers containing -SO3 -, -CONH2 and oxethyl (EO) groups by free radical micellar copolymerization. The structure and thermal stability of terpolymers were characterized by IR and differential thermal analysis (DTA), respectively. The surface activities of polymers in distilled water and in the presence of inorganic salt in aqueous medium were evaluated. The effects of the monomer ratio on properties were also discussed. The results show that the synthesized bipolymer (PMOPnS) has good water solubility and surface activity, and the bipolymer with molar ratio of active monomers (MOP1000∶AMPS) of 1∶2 has a lower surface tension than the one with a molar ratio of 1∶4. The terpolymer becomes to decompose above 258 ℃. The effects of the molar ratio of monomers and the salt mass concentration on the viscosity of terpolymer solution were investigated. PMOPSA-1, a terpolymer of n(MOP1000) ∶n(AMPS) ∶n(AM)=0.5∶1∶98.5, has good thickening effect and surface/interfacial activity. The viscosities of 2% terpolymer in distilled water and in 2% NaCl solution at 30 ℃ are 1 108 and 1 157 mPa·s, respectively. The surface tension at 30 ℃ and the interfacial tension against kerosene at 45 ℃ for 2% aqueous terpolymer solution in the presence of 2%NaCl+0.1%CaCl2 are 30.43 and 2.09 mN/m, respectively, indicating that PMOPSA-1 has good thermal stability, thickening property and surface/interfacial activity.

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    糖基双子阳离子表面活性剂杀菌性能
    Bactericidal activity of sugar-based cationic gemini surfactants
    王军,杨许召,陈玉菲,邹文苑
    2019 (2):  83-86.  doi: 10.3969/j.issn.1001-1803.2019.02.004
    摘要 ( 403 )   HTML ( 11 )   PDF(981KB) ( 368 )  

    利用抑菌圈法对糖基双子阳离子表面活性剂(SGCS)和糖基阳离子表面活性剂(SCS)对大肠杆菌(E.coli)和金黄色葡萄球菌的抑菌性能进行了评价。SGCS的抑菌性能优于SCS;抑菌圈随着SGCS碳链增长先增大后变小,C12-SGCS具有较佳的抑菌性能。C12-SGCS和C12-SCS对硫酸盐还原菌(SRB)、铁细菌(FEB)、腐生菌菌群(TGB)、E.coli和禾谷镰刀菌的杀菌性能表明,C12-SGCS的杀菌性能优于C12-SCS,当C12-SGCS的质量浓度为15 mg/L时对SRB,FEB和TGB的杀菌率均超过99%。SGCS抑菌杀菌更广谱高效,具有良好的应用前景。

    The antibacterial activities of sugar-based cationic gemini surfactants (SGCS) and sugar-based cationic surfactants (SCS) against Escherichia coli E.coli) and Staphylococcus aureus were determined by the inhibition zone method. The antibacterial activity of SGCS is better than that of SCS. The inhibition zone of SGCS is increased and then decreased with the increasing carbon chain length of SGCS, and C12-SGCS has the optimum antibacterial activity. The bactericidal activities of C12-SGCG and C12-SCS against sulfate reducing bacteria (SRB) , Ferribacteriales (FEB) , Saprophytic bacteria group (TGB), E.coli and Fusarium graminearum were evaluated. The bactericidal activity of C12-SGCS is better than that of C12-SCS. The bactericidal rates of C12-SGCS at 15 mg/L against SRB, FEB and TGB are all above 99%. SGCS has a good application prospect because of its broad spectrum and high efficiency in bactericidal and antibacterial actions.

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    弱凝胶调驱体系性能评价研究
    Evaluation of the performance of weak-gel profile-controlling and flooding system
    张继红,冯建祎
    2019 (2):  87-91.  doi: 10.3969/j.issn.1001-1803.2019.02.005
    摘要 ( 359 )   HTML ( 6 )   PDF(1061KB) ( 469 )  

    针对具有储层非均质性强、渗透率低和孔隙结构复杂特点的储层,在注水开发后期,含水率急剧上升,普通的水驱和聚驱方法很难将油驱替出。复合离子型聚合物凝胶有很好的储层适应性,与注入污水配伍性好,成胶时间可控,吸附、滞留能力强,抗冲刷性好。其注入能力强,波及范围大,既可以封堵储层大孔道("调"的作用),又可以驱替储层剩余油("驱"的作用),能够满足调驱体系大剂量注入的要求。本文针对复合离子型凝胶调驱体系进行配方优选并进行性能评价实验,实验结果表明,该调驱体系具有较好的抗盐性、抗剪切性、热稳定性和黏弹性。

    For reservoirs with high heterogeneity, low permeability and complex pore structure, the water cut sharply increases in the late-stage development by water injection, and ordinary water flooding and polymer flooding methods are difficult to obtain oil. In contrast, the composite ionic polymer gel has good reservoir adaptability, good compatibility with injected sewage, controllable gelation time, strong adsorption and retention capacity, and good resistance to erosion. Its strong injection ability and wide spread range can not only seal the large pores of the reservoir (namely "profile-controlling"), but also can drive the remaining oil in the reservoir (namely "flooding"), and thus can meet the requirements of large-dose injection of the profile-controlling and flooding system. In this paper, formula optimization and performance evaluation were both carried out for the profile-controlling and flooding system based on composite ionic gel. The experimental results show that the system has good salt resistance, shear resistance, thermal stability and viscoelasticity.

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    包覆3种紫外线吸收剂的防晒微胶囊的制备及性能研究
    Preparation and properties of sunscreen microcapsules containing with 3 kinds of ultraviolet absorbents
    袁舒畅,康园园,余林林,李雪婷,鲁希华
    2019 (2):  92-97.  doi: 10.3969/j.issn.1001-1803.2019.02.006
    摘要 ( 515 )   HTML ( 20 )   PDF(2193KB) ( 424 )  

    采用界面自由基聚合法制备了以聚二甲基丙烯酸乙二醇酯 (PEGDMA) 为壁材,紫外线吸收剂胡莫柳酯 (HMS) 、阿伏苯宗 (AVB) 和奥克立林 (OCT) 的混合物为芯材的微胶囊。利用光学显微镜 (OM) 探究了不同芯材比和不同壁材含量对微胶囊形貌的影响。用傅里叶红外光谱 (FT-IR) 、纳米粒度与电位分析仪(Nano-zs) 和扫描电镜 (SEM) 分别对微胶囊的化学结构、粒径分布和形貌进行了表征。利用热重分析仪 (TGA) 分析了微胶囊的热稳定性并测定了包埋率。通过紫外线透过率分析仪测试其SPF值。结果表明,芯材中3种紫外线吸收剂 m (AVB) ∶m (OCT) ∶m (HMS) =1∶2∶3,壁材质量分数为6%时,制备的微胶囊为饱满的球形,测得该体系中芯材的包埋率为73.55%。与未包覆的HMS、AVB和OCT混合物SPF值相比,防晒微胶囊SPF值显著提高。

    The sunscreen microcapsules were prepared by interfacial free-radical polymerization, with poly (ethylene glycol) dimethacrylate (PEGDMA) as shell material and the mixture of homosalate (HMS), avobenzone (AVB) and octocrilene (OCT) as core material. The morphologies of PEGDMA microcapsules prepared at different core composition and with different amounts of shell were explored by optical microscope (OM). The chemical structure, particle size distribution and the morphology of microcapsules were characterized by FT-IR, particle size & zeta potential analyzer (Nano-zs) and scanning electron microscope (SEM), respectively. The thermal stability of microcapsules and encapsulation efficiency were obtained by thermogravimetric analysis (TGA). The values of sun protection factor (SPF) of microcapsules were measured on a UV transmittance analyzer. The results show that when m(AVB) ∶m(OCT) ∶m(HMS)=1∶2∶3 in the core, and the mass concentration of PEGDMA (the material for building shell) is 6%, the microcapsules thus prepared will have a spherical morphology, indicative of an encapsulation efficiency of 73.55%. Moreover, the sunscreen microcapsules lead to obviously higher SPF values compared with the naked mixture of HMS, AVB and OCT in sunscreen creams.

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    咖啡酸的化学改性及产物抗氧化性的研究
    Synthesis and the antioxidation study of the chemically modified derivatives of caffeic acid
    王东,赵雪,宋京九,祝钧
    2019 (2):  98-102.  doi: 10.3969/j.issn.1001-1803.2019.02.007
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    以咖啡酸和氨基酸乙酯盐酸盐为原料,1-(3-二甲基氨基丙基)-3-乙基碳二亚胺盐酸盐(EDC)及1-羟基苯并三唑(HOBt)为催化剂,合成咖啡酰甘氨酸乙酯、咖啡酰丙氨酸乙酯、咖啡酰丝氨酸乙酯、咖啡酰苏氨酸乙酯4种产物。利用核磁共振氢谱( 1H NMR)和高效液相色谱-质谱(HPLC-MS)对产物结构进行表征,考察了咖啡酸化学改性产物对DPPH自由基及羟基自由基活性的抑制率及对红细胞膜的刺激性,并与咖啡酸单体进行了比较。结果表明,通过在咖啡酸中引入甘氨酸乙酯、丙氨酸乙酯、丝氨酸乙酯和苏氨酸乙酯后,4种咖啡酸酰胺类产物均呈现较好的抑制DPPH自由基、羟基自由基活性的效果;咖啡酰丝氨酸乙酯清除DPPH自由基能力较强,其IC50值为13.5 μmol/L;咖啡酰丙氨酸乙酯清除羟基自由基能力较强,其IC50值为0.214 mmol/L。红细胞溶血试验结果表明,4种咖啡酸酰胺类衍生物的红细胞溶血率均低于咖啡酸单体。

    Caffeoyl glycine ethyl ester, caffeoyl alanine ethyl ester, caffeoyl serine ethyl ester and caffeoyl threonine ethyl ester were synthesized from L-amino acid ethyl ester hydrochloride with caffeic acid in the presence of a catalytic amount of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) and 1-hydroxybenzotriazole (HOBt) . The structure of the products after the reaction was characterized by 1H NMR and HPLC-MS. The inhibitory rates against DPPH radical and hydroxyl radical and the erythrocyte membrane irritation were investigated for the chemically modified products of caffeic acid which were compared with caffeic acid. The results show that all these four caffeic acid amide derivatives show good inhibition against DPPH radicals and hydroxyl radicals, which have introduced glycine ethyl ester, alanine ethyl ester, serine ethyl ester, and threonine ethyl ester in the molecular structure of caffeic acid. The caffeic acid amide derived from serine ethyl ester has the strongest scavenging activity against DPPH free radicals (IC50=13.5 μmol/L), while the one derived from alanine ethyl ester is the strongest in scavenging hydroxyl radicals with an IC50value of 0.214 mmol/L. The results of red blood cell hemolysis show that all these four caffeic acid amide derivatives exihibit lower hemolysis ratios than caffeic acid.

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    蛋白酶在洗衣液中的稳定性改良
    Improvement of proteases stability in liquid laundry detergent
    吴美娜,李磊,夏咏梅,刘湘,王海军
    2019 (2):  103-107.  doi: 10.3969/j.issn.1001-1803.2019.02.008
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    以硼砂为对照,考察了16种柠檬酸盐、多元醇及酯系列稳定剂,以及温度、pH、稳定剂用量对3种蛋白酶在洗衣液中稳定性的影响;同时基于洗衣液的主要成分考察了表面活性剂AES,AEO和APG等对蛋白酶活的影响。实验结果表明,柠檬酸盐尤其是柠檬酸铵钙的稳定效果最佳,APG0810和APG1214的稳定效果与硼砂接近。当蛋白酶用量为0.5%时,以柠檬酸铵钙-APG0810-APG1214三元复合体系稳定蛋白酶,含有Purafect 4000L和Purafect Prime 4000L的复合稳定剂体系在pH=7和25 ℃下的3周酶活保持率分别可达到84.3%和71.5%;在pH=8和37 ℃下的3周酶活保持率分别为47.2%和30.4%;硼砂体系pH=7和37 ℃下的3周酶活保持率分别为2.87%和13.5%。此外,AES会较大幅度地降低酶活,而非离子表面活性剂AEO7和AEO9对其酶活无显著影响,但AEO和AES的混合并不能降低AES对酶活的损伤,可以考虑在液体加酶洗涤剂中增加APG和AEO的使用。

    With borax as control, the effects of 16 stabilizers of citrate, polyols and esters, temperature, pH and amount of stabilizer on the stability of three proteases in liquid laundry detergent were investigated, and the effects of surfactants AES, AEO and APG on the activity of protease were also investigated based on the main components of liquid laundry detergent. Results show that the stability of citrate, especially calcium ammonium citrate, is the best, and the stability of APG0810 and APG1214 is close to that of borax. When the amount of protease was 0.5%, the three-week activity retention rates of protease stabilized by calcium ammonium citrate-APG0810-APG1214 ternary complex stabilizer system, Purafect 4000L and Purafect Prime 4000L complex stabilizer at pH=7 and 25 ℃ were 84.3% and 71.5%, respectively; the three-week activity retention rates at pH=8 and 37 ℃ were 47.2% and 30.4%, respectively; and the three-week activity retention rates of protease stabilized by borax at pH=7 and 37 ℃ were 2.87% and 13.5%, respectively. In addition, AES can significantly reduce the enzyme activity, while non-ionic surfactants AEO7 and AEO9 did not. However, the mixing of AEO and AES cannot reduce the damage of AES to the enzyme activity. It can be considered to increase the use of APG and AEO in liquid enzyme-enhanced detergents.

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    过氧磷钨酸季铵盐催化合成环氧柏木烷
    Synthesis of epoxycedrane catalyzed by quaternary ammonium peroxy phosphotungstate
    高炜琳,朱凯
    2019 (2):  108-112.  doi: 10.3969/j.issn.1001-1803.2019.02.009
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    以钨酸钠、磷酸、过氧化氢(H2O2)和十六烷基三甲基氯化铵为原料制备了过氧磷钨酸季铵盐催化剂。通过FT-IR、TG对催化剂进行了结构和热稳定性的表征。在H2O2为氧化剂,无溶剂条件下,采用过氧磷钨酸季铵盐催化α-柏木烯环氧化合成环氧柏木烷。考察了各反应条件对环氧化反应的影响。结果表明,在反应温度60 ℃,反应时间3.5 h,H2O2α-柏木烯摩尔比为1∶2,催化剂过氧磷钨酸季铵盐用量3.0% (以H2O2质量计,下同),助剂Na2HPO4用量1.6%条件下,环氧柏木烷的收率为65.7%,α-柏木烯的转化率为90.1%,环氧产物选择性可达72.9%。

    A catalyst, namely quaternary ammonium peroxy phosphotungstate, was prepared using sodium tungstate, phosphoric acid, hydrogen peroxide and cetyltrimethylammonium chloride. The structure and thermal stability of the catalyst were characterized by infrared spectroscopy (FT-IR) and thermogravimetric analysis (TG). The synthesized catalyst was used in the epoxidation of α-cedrene using H2O2 as oxidant and without any solvent. The effects of reaction conditions on the epoxidation were studied. The optimized reaction conditions were obtained as follows: the reaction temperature was 60 ℃; the reaction time was 3.5 h; the molar ratio of raw materials was n(H2O2)∶nα-cedrene)=1∶2; the catalyst and cocatalyst (Na2HPO4) were added in the amounts corresponding to 3.0% and 1.6% of H2O2, respectively. Meanwhile, the yield of epoxycedrane, the conversion of α-cedrene and the epoxy-product selectivity were 65.7%, 90.1% and 72.9%, respectively.

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    专论与综述
    皮肤黑色素形成机理与干预机制
    Mechanism of skin melanin formation and its intervention
    陈卓仪,刘晓英,郑雅婷,洪婷,刘潭林,杜志云
    2019 (2):  113-117.  doi: 10.3969/j.issn.1001-1803.2019.02.010
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    皮肤黑色素形成机理与美白研究息息相关,综述了皮肤黑色素的形成机理及其在细胞水平上的调控,同时也对黑色素的干预机制,包括黑色素合成通路、运输路径、分解及代谢和内外因素干预调节多方面进行深入分析。最后,对皮肤黑色素未来研究趋势进行展望。

    The mechanism of skin melanin formation is closely related to the study of whitening. Therefore, the formation mechanism of skin melanin and its regulation at the cellular level were reviewed. The intervention mechanism of melanin, including the synthesis pathway, transportation pathway, decomposition and metabolism, and the intervention and regulation of internal and external factors were also deeply analyzed. Finally, the future research trend of skin melanin was prospected.

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    灵芝美容护肤作用机制及其在化妆品行业中的发展现状
    Cosmetic mechanisms of Ganoderma lucidum and itsdevelopment in cosmetics
    王倩,张佳婵,王昌涛,安全
    2019 (2):  118-125.  doi: 10.3969/j.issn.1001-1803.2019.02.011
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    通过对不同产地、不同生长条件以及不同种属和部位灵芝成分的综述,阐明了不同条件下灵芝成分的差异性;概述了灵芝的美容护肤机制,总结了现阶段含灵芝的化妆品品牌及成分,并分析了市场中灵芝化妆品的开发缺陷以及技术上的不足,旨在为灵芝在化妆品中的应用提供一定的理论基础。

    The differences of components of Ganoderma lucidum from different origins, different growth conditions, different species and parts were summarized. The molecular mechanisms and the cosmetic brands and ingredients containing Ganoderma lucidum at the current stage were outlined in this review. Then, we pointed out its development defects and technical deficiencies in the market through the above analysis. This review aims to lay a certain theoretical foundation for the application of Ganoderma lucidum in cosmetics.

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    分析与检测
    气相色谱法测定防晒化妆品中14种防晒剂的含量
    Determination of 14 sunscreen agents in sunscreen cosmetics by gas chromatography
    朱惠斌,王雪平
    2019 (2):  126-131.  doi: 10.3969/j.issn.1001-1803.2019.02.012
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    采用甲醇超声萃取防晒化妆品中防晒剂,经DB-5MS毛细管色谱柱分离,氢火焰离子化检测器测定,建立了气相色谱法同时测定防晒化妆品中14种防晒剂的检测方法。结果表明:14种防晒剂在0.5~100.0 mg/kg范围内线性关系良好,相关系数(r 2)≥0.999 3;检出限为0.05~0.15 mg/kg,定量限为0.17~0.50 mg/kg;加标回收率为91. 7%~100.1%,相对标准偏差为1.1%~3.1%。该法操作简便、加标回收率高、精密度好、检出限低,可为防晒化妆品中防晒剂的种类和含量测定提供参考。

    A method for simultaneous determination of 14 sunscreen agents in sunscreen cosmetics was established by gas chromatography, with ultrasonic extraction of sunscreen agents in sunscreen cosmetics carried out by DB-5MS capillary column separation and hydrogen flame ionization detector. The results show that the linearity of 14 sunscreen agents is good in the range of 0.5-100.0 mg/kg, and the correlation coefficients are more than 0.999 3. The detection limit is 0.05-0.15 mg/kg, the limit of quantification is 0.17-0.50 mg/kg; the relative standard deviation is 1.1%-3.1%, and the recovery rate of the spiked standards are 91.7%-100.1%. The method has the advantages of simple operation, high recovery rate, good precision and low detection limit, and can provide a detection method for determining the type and content of the sunscreen agent in the sunscreen cosmetic.

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    高效液相色谱法测定化妆品中辛酰羟肟酸的含量
    Determination of octyl hydroxamic acid in cosmetics by high performance liquid chromatography
    李法锦,李适炜,刘瑞学,冷群英
    2019 (2):  132-134.  doi: 10.3969/j.issn.1001-1803.2019.02.013
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    建立了高效液相色谱法测定化妆品中辛酰羟肟酸含量的分析方法。采用ZORBAX Eclipse Plus C18柱(4.6 mm×250 mm,5 μm),流动相为水-乙腈,流速1.0 mL/min,柱温25 ℃,检测波长220 nm,进样量10 μL。结果表明,辛酰羟肟酸在10~200 mg/L范围内,峰面积与质量浓度呈良好的线性关系,相关系数为0.999 9 (n=5),方法检出限为5 mg/kg。高、中、低不同水平的加标回收率为96.28%~101.23%,相对标准偏差≤2.43%。该方法操作简便、精密度高、回收率高、重现性好,可用于化妆品中辛酰羟肟酸的检测。

    A method for the determination of octyl hydroxamic acid in cosmetics by high performance liquid chromatography (HPLC) was established. ZORBAX Eclipse Plus C18 column (4.6 mm×250 mm, 5 μm) was used. The mobile phase was water and acetonitrile, the flow rate was 1.0 mL/min, the column temperature was 25 ℃, the detection wavelength was 220 nm and the injection volume was 10 μL. The results show that the peak area has a good linear relationship with the mass concentration of octanoyl hydroxamic acid in the range of 10-200 mg/L, and the correlation coefficient is 0.999 9 (n=5). The limit of detection is 5 mg/kg. The recoveries of octyl hydroxamic acid at different spiked levels are 96.28%-101.23% with the relative standard deviations (RSD) less than 2.43%. This method is simple operation, high precision, high recovery and good reproducibility, and can be used to detect octyl hydroxamic acid in cosmetics.

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