CN112336671A - 一种护肤消毒液及制备方法 - Google Patents
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Abstract
本发明涉及日用品技术领域,公开了一种护肤消毒液及制备方法,包括A组分、B组分、C组分和D组分,所述A组分包括8%~10%十二烷基苯磺酸钠、12%~15%月桂醇聚醚硫酸酯钠、2%~3%椰油酰胺丙基甜菜碱、2%~3%椰油酰胺DEA、1%~2%EDTA二钠和1%~2%珠光剂,还公开了一种护肤消毒液的制备方法,包括以下步骤:S1、称取A组分溶于反应釜内;S2、称取C组分溶于反应釜内,调节PH值;S3、称取D组分溶于反应釜内,调节PH值和粘度;S4、称取D组分溶于反应釜内。本发明通过十二烷基苯磺酸钠、月桂醇聚醚硫酸酯钠、椰油酰胺丙基甜菜碱、椰油酰胺DEA、EDTA二钠和珠光剂配置而成,具有较强的消毒能力,且对人体的舒适感、去油污效果、温和性均较佳。
Description
技术领域
本发明涉及日用品技术领域,具体是一种护肤消毒液及制备方法。
背景技术
随着人们安全、环保意识的提高,越来越多的人们开始注意洗手消毒,因为,手机、钱和一些公共场合的公用品都充满肉眼看不到的脏东西和细菌,人的皮肤、物体表面以及环境中的消毒是控制因细菌引起感染的有效手段,而这就需要使用消毒液。
中国专利公开了一种医用免洗手护肤消毒液及其制备方法(授权公告号CN106214573B),该专利技术能迅速有效地杀灭手掌及指缝间的各种细菌及病毒,杀菌效果显著,而且免水洗手,使用及携带方便,随时随地都可以清洁双手;pH值接近皮肤的pH,对正常皮肤无毒无刺激,安全高效,但是其舒适感去油污效果、温和性均不佳,且杀菌效率不高。
发明内容
本发明的目的在于提供一种护肤消毒液及制备方法,以解决上述背景技术中提出的问题。
为实现上述目的,本发明提供如下技术方案:
一种护肤消毒液,包括A组分、B组分、C组分和D组分,所述A组分包括8%~10%十二烷基苯磺酸钠、12%~15%月桂醇聚醚硫酸酯钠、2%~3%椰油酰胺丙基甜菜碱、2%~3%椰油酰胺DEA、1%~2%EDTA二钠和1%~2%珠光剂,所述B组分包括2%~3%柠檬酸、2%~3%氢氧化钠和1%~1.5%氯化钠,所述C组分包括3%~5%甘油、4%~5%木立芦荟叶提取物和0.5%~0.8%植物香精,所述D组分包括3%~4%聚乙烯醇、3%~4%2-丙醇和1%~2%AEO-9,所述E组分包括0.1%~0.2%DMDM乙内酰脲和0.2%~0.3%山梨酸钾。
作为本发明再进一步的方案:所述A组分还可以包括12%~15%对氯间二甲苯酚、2%~3%丙烯酸羊毛脂、8%~10%山梨糖醇酐单硬脂酸酯、8%~10%聚氧乙烯山梨醇酐单硬脂酸酯和1%~1.5%羧甲基纤维素。
作为本发明再进一步的方案:所述E组分还可以包括0.05%~0.1%苯甲酸、0.1%~0.2%丁基羟基茴香醚和0.1%~0.2%二丁基羟基甲苯。
作为本发明再进一步的方案:所述珠光剂包括35%~40%硬脂酸乙二醇双酯、35%~40%硬脂酸乙二醇单酯和20%~30%十二醇。
一种护肤消毒液的制备方法,包括以下步骤:
S1、先称取40%重量比的去离子水加入反应釜内,再依次称取8%重量比的十二烷基苯磺酸钠、13%重量比的月桂醇聚醚硫酸酯钠、2%重量比的椰油酰胺丙基甜菜碱、2%重量比的椰油酰胺DEA、2%重量比的EDTA二钠和2%重量比的珠光剂,加入到反应釜内,在加入的过程中不断搅拌,升温至65~70℃,继续搅拌15~20min,使其溶解成透明粘液;
S2、降至室温后,依次称取4%重量比的甘油、5%重量比的木立芦荟叶提取物和0.7%重量比的植物香精,加入到反应釜内进行搅拌,使其溶解后测量其PH值,根据需要加入氢氧化钠调节溶液的PH值;
S3、依次称取3%重量比的聚乙烯醇、3%重量比的2-丙醇和1%重量比的AEO-9,加入到反应釜内进行搅拌,使其溶解后测量其PH值和粘度,根据需要加入柠檬酸调节溶液的PH值,加入氯化钠调节溶液的粘度;
S4、依次称取0.1%重量比的DMDM乙内酰脲和0.2%重量比的山梨酸钾,加入到反应釜内进行搅拌均匀即可;
作为本发明再进一步的方案:所述步骤S2中PH值保持在7.0~8.0之间,所述步骤S3中PH值保持在5.5~6.5之间,且步骤S3中粘度保持在0.15~0.18Pa﹒S之间。
作为本发明再进一步的方案:所述步骤S1中升温的速度为3~5℃/min,所述反应釜的搅拌速度控制在35~45r/min之间。
与现有技术组分比,本发明的有益效果:
本发明通过十二烷基苯磺酸钠、月桂醇聚醚硫酸酯钠、椰油酰胺丙基甜菜碱、椰油酰胺DEA、EDTA二钠和珠光剂以及部分辅料进行配置而成,具有较强的消毒能力,对大肠杆菌和金黄色葡萄球菌均有较强的杀菌能力,且对人体的去油污效果、温和性均较佳,对人体副作用小,且生产、制备简单,能耗较低,可以大规模生产,具有较好的经济效益。
具体实施方式
实施例一
本发明实施例中,一种护肤消毒液,包括A组分、B组分、C组分和D组分,A组分包括8%~10%十二烷基苯磺酸钠、12%~15%月桂醇聚醚硫酸酯钠、2%~3%椰油酰胺丙基甜菜碱、2%~3%椰油酰胺DEA、1%~2%EDTA二钠和1%~2%珠光剂,B组分包括2%~3%柠檬酸、2%~3%氢氧化钠和1%~1.5%氯化钠,C组分包括3%~5%甘油、4%~5%木立芦荟叶提取物和0.5%~0.8%植物香精,D组分包括3%~4%聚乙烯醇、3%~4%2-丙醇和1%~2%AEO-9(脂肪醇聚氧乙烯醚),E组分包括0.1%~0.2%DMDM乙内酰脲和0.2%~0.3%山梨酸钾,珠光剂包括35%~40%硬脂酸乙二醇双酯、35%~40%硬脂酸乙二醇单酯和20%~30%十二醇。
实施例二
本发明实施例中,一种护肤消毒液,包括A组分、B组分、C组分和D组分,A组分包括12%~15%对氯间二甲苯酚、2%~3%丙烯酸羊毛脂、8%~10%山梨糖醇酐单硬脂酸酯、8%~10%聚氧乙烯山梨醇酐单硬脂酸酯和1%~1.5%羧甲基纤维素,B组分包括2%~3%柠檬酸、2%~3%氢氧化钠和1%~1.5%氯化钠,C组分包括3%~5%甘油、4%~5%木立芦荟叶提取物和0.5%~0.8%植物香精,D组分包括3%~4%聚乙烯醇、3%~4%2-丙醇和1%~2%AEO-9(脂肪醇聚氧乙烯醚),E组分包括0.1%~0.2%DMDM乙内酰脲和0.2%~0.3%山梨酸钾,珠光剂包括35%~40%硬脂酸乙二醇双酯、35%~40%硬脂酸乙二醇单酯和20%~30%十二醇。
实施例二
本发明实施例中,一种护肤消毒液,包括A组分、B组分、C组分和D组分,A组分包括12%~15%对氯间二甲苯酚、2%~3%丙烯酸羊毛脂、8%~10%山梨糖醇酐单硬脂酸酯、8%~10%聚氧乙烯山梨醇酐单硬脂酸酯和1%~1.5%羧甲基纤维素,B组分包括2%~3%柠檬酸、2%~3%氢氧化钠和1%~1.5%氯化钠,C组分包括3%~5%甘油、4%~5%木立芦荟叶提取物和0.5%~0.8%植物香精,D组分包括3%~4%聚乙烯醇、3%~4%2-丙醇和1%~2%AEO-9(脂肪醇聚氧乙烯醚),E组分还可以包括0.05%~0.1%苯甲酸、0.1%~0.2%丁基羟基茴香醚和0.1%~0.2%二丁基羟基甲苯,珠光剂包括35%~40%硬脂酸乙二醇双酯、35%~40%硬脂酸乙二醇单酯和20%~30%十二醇。
在实施例一中,一种护肤消毒液的制备方法,包括以下步骤:
S1、先称取40%重量比的去离子水加入反应釜内,再依次称取8%重量比的十二烷基苯磺酸钠、13%重量比的月桂醇聚醚硫酸酯钠、2%重量比的椰油酰胺丙基甜菜碱、2%重量比的椰油酰胺DEA、2%重量比的EDTA二钠和2%重量比的珠光剂,加入到反应釜内,在加入的过程中不断搅拌,升温至65~70℃,继续搅拌15~20min,使其溶解成透明粘液;
S2、降至室温后,依次称取4%重量比的甘油、5%重量比的木立芦荟叶提取物和0.7%重量比的植物香精,加入到反应釜内进行搅拌,使其溶解后测量其PH值,根据需要加入氢氧化钠调节溶液的PH值;
S3、依次称取3%重量比的聚乙烯醇、3%重量比的2-丙醇和1%重量比的AEO-9,加入到反应釜内进行搅拌,使其溶解后测量其PH值和粘度,根据需要加入柠檬酸调节溶液的PH值,加入氯化钠调节溶液的粘度;
S4、依次称取0.1%重量比的DMDM乙内酰脲和0.2%重量比的山梨酸钾,加入到反应釜内进行搅拌均匀即可;
优先的,步骤S2中PH值保持在7.0~8.0之间,步骤S3中PH值保持在5.5~6.5之间,且步骤S3中粘度保持在0.15~0.18Pa﹒S之间。
优先的,步骤S1中升温的速度为3~5℃/min,反应釜的搅拌速度控制在35~45r/min之间。
为了更好地说明本发明的技术效果,通过下述实施例(实施例一、实施例二和实施例三)和对比例(对比例一、对比例二和对比例三)实验进行阐述:
对比例一、对比例二、对比例三:市场上随机抽选三款不同品牌的护肤消毒液
一、分别检测对比例一、对比例二、对比例三、实施例一、实施例二和实施例三中消毒液的感官指标和有害物质(砷(As,mg/kg)和铅(Pb,mg/kg)含量,并把检测的结果与国标进行对比,国标采用的是中华人民共和国卫生部发布的《中华人民共和国国家标准》食品安全国家标准—消毒剂GB 14930.2—2012号文件技术要求,对比例一、对比例二、对比例三、实施例一、实施例二和实施例三与国标的指标,见表1。
表1:对比例一、对比例二、对比例三、实施例一、实施例二和实施例三与国标的指标比较:
从表1分析可以得出:对比例一、对比例二、对比例三、实施例一、实施例二和实施例三的外观均为无分层、无悬浮物和无沉淀,满足国标的要求,对比例一、对比例二、对比例三、实施例一、实施例二和实施例三的As含量均小于3mg/kg,Pb含量均小于30mg/kg,满足国标的要求,均为合格产品。
二、分别检测对比例一、对比例二、对比例三、实施例一、实施例二和实施例三中消毒液使用后的效果
把实验者分成六组,每组10人,分别使用对比例一、对比例二、对比例三、实施例一、实施例二和实施例三中的消毒液进行洗手,冲洗后对消毒液的舒适感、去油污效果、温和性进行打分,每个指标按5级评分法进行评估打分,优秀为5分,良好为4分,较好为3分,一般为2分,较差为1分,并计算其平均值,对比例一、对比例二、对比例三、实施例一、实施例二和实施例三效果评分,见表2。
表2:对比例一、对比例二、对比例三、实施例一、实施例二和实施例三的效果评分比较:
从表3分析可以得出:实施例一、实施例二和实施例三人体的舒适感、去油污效果和温和性评分均高于对比例一、对比例二和对比例三人体的舒适感、去油污效果和温和性评分,其中实施例一中舒适感、去油污效果和温和性评分均最高,从而得出实施例一具有较佳的舒适感、去油污效果和温和性。
三、分别检测对比例一、对比例二、对比例三、实施例一、实施例二和实施例三中消毒液的杀菌效果
选取实验用菌悬液中大肠杆菌的浓度为1.75×107cfu/ml,金黄色葡萄球菌的浓度为2.10×106cfu/ml,消毒剂的浓度为3%;
取消毒试验用无菌试管,先加入0.5ml实验用菌悬液(大肠杆菌和金黄色葡萄球菌),再加入0.5ml有机干扰物质(3%(单位体积内所含的质量)牛血清白蛋白贮存溶液),均匀混合后,置20±1℃下水浴5min后,用无菌吸管吸取4.0ml上述浓度的消毒液注入其中,迅速均匀混合后记录下时间,待实验用菌悬液与消毒液作用5min后,分别吸取0,5ml混合液与4.5ml灭菌的中和剂,一起加入到另一只无菌试管中,混合均匀,10min后吸取1.0ml试样,按照活菌培养计数的方法测定存活菌数(大肠杆菌和金黄色葡萄球菌);
按照上述方法利用稀释液代替消毒液,进行平行试验,作为阳性对照组,所有试样均在37℃恒温箱中培养48h后,观察最终结果,记录各组活菌量,并计算杀菌数值,对比例一、对比例二、对比例三、实施例一、实施例二和实施例三与对照组的指标,见表3。
表3、对比例一、对比例二、对比例三、实施例一、实施例二和实施例三与对照组的指标比较
从表3分析可以得出:对照组在没有消毒液的情况下,大肠杆菌和金黄色葡萄球菌自由生长,培养后,浓度分别为4.26×109cfu/ml和8.53×107cfu/ml,对比例一、对比例二、对比例三、实施例一、实施例二和实施例三杀菌效率均大于>99.9%,从而得出其均有较好的杀菌性能,但大肠杆菌在实施例一、实施例二和实施例三中的存活量浓度均小于对比例一、对比例二和对比例三中的存活量浓度,其中实施例一中大肠杆菌的存活量浓度最低,金黄色葡萄球菌在实施例一、实施例二和实施例三中的存活量浓度也均小于对比例一、对比例二和对比例三中的存活量浓度,其中实施例一中金黄色葡萄球菌的存活量浓度也是最低,从而得出实施例一具有最佳杀菌效果。
以上所述的,仅为本发明较佳的具体实施方式,但本发明的保护范围并不局限于此,任何熟悉本技术领域的技术人员在本发明揭露的技术范围内,根据本发明的技术方案及其发明构思加以等同替换或改变,都应涵盖在本发明的保护范围之内。
Claims (7)
1.一种护肤消毒液,包括A组分、B组分、C组分和D组分,其特征在于,所述A组分包括8%~10%十二烷基苯磺酸钠、12%~15%月桂醇聚醚硫酸酯钠、2%~3%椰油酰胺丙基甜菜碱、2%~3%椰油酰胺DEA、1%~2%EDTA二钠和1%~2%珠光剂,所述B组分包括2%~3%柠檬酸、2%~3%氢氧化钠和1%~1.5%氯化钠,所述C组分包括3%~5%甘油、4%~5%木立芦荟叶提取物和0.5%~0.8%植物香精,所述D组分包括3%~4%聚乙烯醇、3%~4%2-丙醇和1%~2%AEO-9,所述E组分包括0.1%~0.2%DMDM乙内酰脲和0.2%~0.3%山梨酸钾。
2.根据权利要求1所述的一种护肤消毒液,其特征在于,所述A组分还可以包括12%~15%对氯间二甲苯酚、2%~3%丙烯酸羊毛脂、8%~10%山梨糖醇酐单硬脂酸酯、8%~10%聚氧乙烯山梨醇酐单硬脂酸酯和1%~1.5%羧甲基纤维素。
3.根据权利要求1所述的一种护肤消毒液,其特征在于,所述E组分还可以包括0.05%~0.1%苯甲酸、0.1%~0.2%丁基羟基茴香醚和0.1%~0.2%二丁基羟基甲苯。
4.根据权利要求1所述的一种护肤消毒液,其特征在于,所述珠光剂包括35%~40%硬脂酸乙二醇双酯、35%~40%硬脂酸乙二醇单酯和20%~30%十二醇。
5.一种制备权利要求1所述护肤消毒液的方法,其特征在于,制备方法包括以下步骤:
S1、先称取40%重量比的去离子水加入反应釜内,再依次称取8%重量比的十二烷基苯磺酸钠、13%重量比的月桂醇聚醚硫酸酯钠、2%重量比的椰油酰胺丙基甜菜碱、2%重量比的椰油酰胺DEA、2%重量比的EDTA二钠和2%重量比的珠光剂,加入到反应釜内,在加入的过程中不断搅拌,升温至65~70℃,继续搅拌15~20min,使其溶解成透明粘液;
S2、降至室温后,依次称取4%重量比的甘油、5%重量比的木立芦荟叶提取物和0.7%重量比的植物香精,加入到反应釜内进行搅拌,使其溶解后测量其PH值,根据需要加入氢氧化钠调节溶液的PH值;
S3、依次称取3%重量比的聚乙烯醇、3%重量比的2-丙醇和1%重量比的AEO-9,加入到反应釜内进行搅拌,使其溶解后测量其PH值和粘度,根据需要加入柠檬酸调节溶液的PH值,加入氯化钠调节溶液的粘度;
S4、依次称取0.1%重量比的DMDM乙内酰脲和0.2%重量比的山梨酸钾,加入到反应釜内进行搅拌均匀即可。
6.根据权利要求5所述的一种护肤消毒液的制备方法,其特征在于,所述步骤S2中PH值保持在7.0~8.0之间,所述步骤S3中PH值保持在5.5~6.5之间,且步骤S3中粘度保持在0.15~0.18Pa﹒S之间。
7.根据权利要求5所述的一种护肤消毒液的制备方法,其特征在于,所述步骤S1中升温的速度为3~5℃/min,所述反应釜的搅拌速度控制在35~45r/min之间。
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