CN106109382A - 氨基酸牙膏制备方法 - Google Patents

氨基酸牙膏制备方法 Download PDF

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CN106109382A
CN106109382A CN201610612174.2A CN201610612174A CN106109382A CN 106109382 A CN106109382 A CN 106109382A CN 201610612174 A CN201610612174 A CN 201610612174A CN 106109382 A CN106109382 A CN 106109382A
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申秋英
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Abstract

本发明公开了一种氨基酸牙膏制备方法,属牙膏技术领域,该方法包括如下步骤:A、将薄荷切碎榨汁;B、当真空制膏机的真空度为‑0.076MPa~‑0.079MPa时,将月桂酰谷氨酸钠、碳酸钙、珍珠粉、牙粉、月桂醇酸钠和木糖醇加入真空制膏机,开动该机的刮刀边进料边搅拌,时间5分钟~8分钟,温度20℃~25℃;C、将薄荷汁加入步骤B的真空制膏机中,搅拌6分钟~7分钟,再静置至膏体消泡;D、保持真空制膏机的真空度为‑0.095MPa,开动真空制膏机对步骤C的膏体进行研磨,时间50分钟~60分钟,静置后分装,即得。本发明提供一种味道清新,具有温和高效清洁、美白牙齿、去除口臭、消除牙龈斑等功效的牙膏。

Description

氨基酸牙膏制备方法
技术领域
本发明涉及口腔清洁护理用品技术领域,尤其是一种氨基酸牙膏制备方法。
背景技术
快节奏的现代生活给人们带来巨大的压力,喝咖啡、喝啤酒、抽烟已成为现代人缓解压力的重要生活方式,而这种生活方式往往会造成人们的牙龈有牙龈斑、黄渍和口臭,影响人们的健康和自信,因此如何解决牙齿温和高效清洁美白的问题已成为口腔清洁护理用品领域的重要课题。
发明内容
本发明所要解决的技术问题是提供一种具有味道清新,温和高效清洁、美白牙齿、去除口臭、消除牙龈斑等功效牙膏的制备方法。
为了解决上述问题,本发明所采用的技术方案是:这种氨基酸牙膏制备方法,采用下列重量份数的原料:
月桂酰谷氨酸钠25份~35份,碳酸钙15份~25份,珍珠粉5份~10份,牙粉2份~5份,月桂醇酸钠1.5份~2份,薄荷0.2份~2份,木糖醇0.01份~0.1份;
包括如下步骤:
A、将薄荷切碎榨汁,备用;
B、当真空制膏机的真空度为-0.076MPa~-0.079MPa时,将月桂酰谷氨酸钠、碳酸钙、珍珠粉、牙粉、月桂醇酸钠、木糖醇加入真空制膏机,开动真空制膏机的刮刀边进料边搅拌,时间5分钟~8分钟,温度20℃~25℃;
C、将薄荷汁液加入步骤B的真空制膏机中,搅拌6分钟~7分钟,然后静置至膏体完全消泡;
D、保持真空制膏机的真空度为-0.095MPa,开动真空制膏机的研磨装置,对步骤C的膏体进行研磨, 时间50分钟~60分钟,静置,经检验合格后分装,即得。
上述技术方案中,更具体的技术方案还可以是:所述牙粉由碳酸钙、水合硅石和磷酸氢钙制成。
进一步的:这种氨基酸牙膏制备方法,采用下列重量份数的原料:
月桂酰谷氨酸钠28份~32份,碳酸钙18份~23份,珍珠粉6份~8份,牙粉2.5份~4.5份,月桂醇酸钠1.6份~1.8份,薄荷0.5份~1.5份,木糖醇0.03份~0.08份。
进一步的:这种氨基酸牙膏制备方法,采用下列重量份数的原料:
月桂酰谷氨酸钠30份,碳酸钙20份,珍珠粉7份,牙粉3份,月桂醇酸钠1.7份,薄荷1份,木糖醇0.05份。
本发明的月桂酰谷氨酸钠是一种氨基酸表面活性剂,弱酸性,泡沫适当、洗涤力强并且能快速的被生物所分解,具有极强的高效清洁能力。
本发明的碳酸钙作为牙膏中的摩擦剂,主要用于增强牙膏的摩擦作用和去污效果。
本发明的珍珠粉珍珠中含有十九种氨基酸、近二十种矿物质和高活性生物牛磺酸与丰富的珍珠蛋白及大量的微量元素,具有促进新城代谢和美白的功效。
本发明的月桂醇酸钠作为牙膏中的乳化剂,同时也是一种强有力的清洁剂。
本发明的薄荷有保持口气清新的作用,能有效去除引起蛀牙的细菌和牙垢,补充牙龈必须的营养成分,美白牙齿,保持牙齿的坚固性,可以由内到外清除牙齿污垢。
本发明的木糖醇作为一种不引起龋齿的五元醇,对于引起牙龈斑的细菌有较为明显的抑制作用。
由于采用了上述技术方案,本发明与现有技术相比具有如下有益效果:
本发明的配方科学合理,成本低廉,对人体无毒害,使用安全可靠;不但温和不刺激,不易损伤牙釉质,而且能够杀菌抑菌,尤其对牙龈斑、牙齿泛黄等问题有显著的改善效果。
具体实施方式
下面结合实施例对本发明作进一步详述:
实施例一
这种氨基酸牙膏制备方法,采用下列重量的原料:
月桂酰谷氨酸钠25公斤,碳酸钙15公斤,5公斤,珍珠粉5公斤,牙粉2公斤,月桂醇酸钠1.5公斤,薄荷0.2公斤,木糖醇0.01公斤;其中牙粉由碳酸钙、水合硅石和磷酸氢钙制成;
包括如下步骤:
A、将薄荷切碎榨汁,备用;
B、当真空制膏机的真空度为-0.076MPaMPa时,将月桂酰谷氨酸钠、碳酸钙、珍珠粉、牙粉、月桂醇酸钠、木糖醇加入真空制膏机中,开动真空制膏机的刮刀边进料边搅拌,时间5分钟,温度20℃~23℃;
C、将薄荷汁液加入步骤B的真空制膏机中,搅拌6分钟,然后静置至膏体完全消泡;
D、保持真空制膏机的真空度为-0.095MPa,开动真空制膏机的研磨装置,对步骤C的膏体进行研磨, 时间50分钟,静置,经检验合格后分装,即得。
实施例二
这种氨基酸牙膏制备方法,采用下列重量的原料:
月桂酰谷氨酸钠35公斤,碳酸钙25公斤,10公斤,珍珠粉10公斤,牙粉5公斤,月桂醇酸钠2公斤,薄荷2公斤,木糖醇0.1公斤;其中,牙粉由碳酸钙、水合硅石和磷酸氢钙制成;
包括如下步骤:
A、将薄荷切碎榨汁,备用;
B、当真空制膏机的真空度为-0.078MPa时,将月桂酰谷氨酸钠、碳酸钙、珍珠粉、牙粉、月桂醇酸钠、木糖醇加入真空制膏机中,开动真空制膏机的刮刀边进料边搅拌,时间8分钟,,温度24℃~25℃;
C、将薄荷汁液加入步骤B的真空制膏机中,搅拌7分钟,然后静置至膏体完全消泡;
D、保持真空制膏机的真空度为-0.095MPa,开动真空制膏机的研磨装置,对步骤C的膏体进行研磨, 时间60分钟,静置,经检验合格后分装,即得。
实施例三
这种氨基酸牙膏制备方法,采用下列重量的原料:
月桂酰谷氨酸钠28份,碳酸钙18份,珍珠粉6份,牙粉2.5份,月桂醇酸钠1.6份,薄荷0.5份,木糖醇0.03份;其中,牙粉由碳酸钙、水合硅石和磷酸氢钙制成;
包括如下步骤:
A、将薄荷切碎榨汁,备用;
B、当真空制膏机的真空度为-0.079MPa时,将月桂酰谷氨酸钠、碳酸钙、珍珠粉、牙粉、月桂醇酸钠、木糖醇加入真空制膏机中,开动真空制膏机的刮刀边进料边搅拌,时间6分钟,,温度20℃~23℃;
C、将薄荷汁液加入步骤B的真空制膏机中,搅拌6.5分钟,然后静置至膏体完全消泡;
D、保持真空制膏机的真空度为-0.095MPa,开动真空制膏机的研磨装置,对步骤C的膏体进行研磨, 时间55分钟,静置,经检验合格后分装,即得。
实施例四
这种氨基酸牙膏制备方法,采用下列重量的原料:
月桂酰谷氨酸钠32份,碳酸钙23份,珍珠粉8份,牙粉4.5份,月桂醇酸钠1.8份,薄荷1.5份,木糖醇0.08份;其余均与实施例一相同。
实施例五
这种氨基酸牙膏制备方法,采用下列重量的原料:
月桂酰谷氨酸钠30公斤,碳酸钙20公斤,珍珠粉7公斤,牙粉3公斤,月桂醇酸钠1.7公斤,薄荷1公斤,木糖醇0.05公斤;其余均与实施例一相同。

Claims (4)

1.一种氨基酸牙膏制备方法在于:采用下列重量份数的原料:
月桂酰谷氨酸钠25份~35份,碳酸钙15份~25份,珍珠粉5份~10份,牙粉2份~5份,月桂醇酸钠1.5份~2份,薄荷0.2份~2份,木糖醇0.01份~0.1份;
包括如下步骤:
A、将薄荷切碎榨汁,备用;
B、当真空制膏机的真空度为-0.076MPa~-0.079MPa时,将月桂酰谷氨酸钠、碳酸钙、珍珠粉、牙粉、月桂醇酸钠、木糖醇加入真空制膏机中,开动真空制膏机的刮刀边进料边搅拌,时间5分钟~8分钟,温度20℃~25℃;
C、将薄荷汁液加入步骤B的真空制膏机中,搅拌6分钟~7分钟,然后静置至膏体完全消泡;
D、保持真空制膏机的真空度为-0.095MPa,开动真空制膏机的研磨装置,对步骤C的膏体进行研磨, 时间50分钟~60分钟,静置,经检验合格后分装,即得。
2.根据权利要求1所述的氨基酸牙膏制备方法,其特征在于:所述牙粉由碳酸钙、水合硅石和磷酸氢钙制成。
3.根据权利要求1或2所述的氨基酸牙膏制备方法,其特征在于:
采用下列重量份数的原料:
月桂酰谷氨酸钠28份~32份,碳酸钙18份~23份,珍珠粉6份~8份,牙粉2.5份~4.5份,月桂醇酸钠1.6份~1.8份,薄荷0.5份~1.5份,木糖醇0.03份~0.08份。
4.根据权利要求1或2所述的氨基酸牙膏制备方法,其特征在于:
采用下列重量份数的原料:
月桂酰谷氨酸钠30份,碳酸钙20份,珍珠粉7份,牙粉3份,月桂醇酸钠1.7份,薄荷1份,木糖醇0.05份。
CN201610612174.2A 2016-07-31 2016-07-31 氨基酸牙膏制备方法 Pending CN106109382A (zh)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108785119A (zh) * 2018-08-16 2018-11-13 江苏雪豹日化有限公司 一种氨基酸生物复合酶牙膏

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Application publication date: 20161116