Novel washing-free hand sanitizer capable of continuously sterilizing

文档序号:1346985 发布日期:2020-07-24 浏览:13次 中文

阅读说明:本技术 一种能够持续杀菌的新型免洗洗手液 (Novel washing-free hand sanitizer capable of continuously sterilizing ) 是由 刘远志 于 2020-05-09 设计创作,主要内容包括:本发明公开了一种能够持续杀菌的新型免洗洗手液,其原料有去离子水配比14.7%-26.7%,乙醇(95%)配比65%-75%,甘油(医用级)配比2-5%,丙二醇1-4%,UIV2000纳米银离子溶液配比4%-6%,卡波姆U20:0.3%-0.4%,三乙醇胺0.15%-0.2%,茶树精油配比0.2%-0.8%,芦荟提取物配比0.5-1.5%,关键点在于采用特定的银离子浓度可以持续抑制细菌并且对手部没有影响,配合其他添加物能够同时保证银离子的体系稳定性,在起到消毒的同时保护双手的作用。(The invention discloses a novel wash-free hand sanitizer capable of continuously sterilizing, which comprises the following raw materials of 14.7-26.7% of deionized water, 65-75% of ethanol (95%), 2-5% of glycerol (medical grade), 1-4% of propylene glycol, 4-6% of UIV2000 nano silver ion solution, carbomer U20: 0.3 to 0.4 percent of the total weight of the composition, 0.15 to 0.2 percent of triethanolamine, 0.2 to 0.8 percent of tea tree essential oil and 0.5 to 1.5 percent of aloe extract, and has the key points that the specific silver ion concentration can continuously inhibit bacteria and has no influence on hands, and the system stability of silver ions can be ensured simultaneously by matching with other additives, thereby playing the role of disinfecting and protecting hands.)

1. A novel no-clean hand sanitizer capable of continuously sterilizing is characterized in that: the raw materials comprise 14.7-26.7% of deionized water, 65-75% of ethanol (95%), 2-5% of glycerin (medical grade), 1-4% of propylene glycol, 4-6% of UIV2000 nano silver ion solution and 4-6% of carbomer U20: 0.3 to 0.4 percent of triethanolamine, 0.15 to 0.2 percent of tea tree essential oil, 0.2 to 0.8 percent of aloe extract and 0.5 to 1.5 percent of aloe extract;

the production process comprises the following steps:

s1, blending and taking U20, and pre-dispersing the U20 into glycerol;

s2, adding deionized water, heating to 80 ℃, and fully stirring;

s3, homogenizing and stirring at 12000RPM for 3 min;

s4, adding absolute ethyl alcohol, and fully stirring and mixing;

s5, mixing triethanolamine and water, 1: 5, after mixing, gradually adding a small amount of the mixture into the main system, and continuously stirring;

s6, observing that the viscosity of the main system meets the requirement, the material body is clear and transparent, stopping adding the mixed solution in the previous step, continuously stirring for 10min, and cooling the material body to the normal temperature;

s7, sequentially adding UIV2000 silver ion solution, tea tree essential oil and aloe extract, and mixing.

2. The novel no-clean hand sanitizer capable of continuously sterilizing as claimed in claim 1, characterized in that: the raw materials comprise 14.7 percent of deionized water, 65 percent of ethanol (95%), 2 percent of glycerin (medical grade), 1 percent of propylene glycol, 4 percent of UIV2000 nano silver ion solution and 4 percent of carbomer U20: 0.3 percent, 0.15 percent of triethanolamine, 0.2 percent of tea tree essential oil and 0.5 percent of aloe extract.

3. The novel no-clean hand sanitizer capable of continuously sterilizing as claimed in claim 1, characterized in that: the raw materials comprise deionized water 18.7%, ethanol 95% 69%, glycerin (medical grade) 3%, propylene glycol 2%, UIV2000 nano silver ion solution 4.6%, carbomer U20: 0.33 percent, 0.17 percent of triethanolamine, 0.4 percent of tea tree essential oil and 0.8 percent of aloe extract.

4. The novel no-clean hand sanitizer capable of continuously sterilizing as claimed in claim 1, characterized in that: the raw materials comprise 22.7 percent of deionized water, 72 percent of ethanol (95%), 4 percent of glycerin (medical grade), 3 percent of propylene glycol, 5.3 percent of UIV2000 nano silver ion solution, and 5.3 percent of carbomer U20: 0.36 percent, 0.19 percent of triethanolamine, 0.6 percent of tea tree essential oil and 1.2 percent of aloe extract.

5. The novel no-clean hand sanitizer capable of continuously sterilizing as claimed in claim 1, characterized in that: the raw materials comprise 26.7 percent of deionized water, 75 percent of ethanol (95%), 5 percent of glycerin (medical grade), 4 percent of propylene glycol, 6 percent of UIV2000 nano silver ion solution and 6 percent of carbomer U20: 0.4 percent of triethanolamine, 0.2 percent of tea tree essential oil and 1.5 percent of aloe extract.

6. The novel no-clean hand sanitizer capable of continuously sterilizing as claimed in claim 1, characterized in that: the action time of the hand sanitizer is 2-20 min.

Technical Field

The invention belongs to the technical field of disinfectants, and mainly relates to a novel no-clean hand sanitizer capable of continuously sterilizing.

Background

The existing no-clean hand sanitizer takes ethanol as a sterilizing substance, but the ethanol is volatile, the sterilization time of hands is extremely limited, the hands can not be sterilized after being volatilized, and other pollutants such as bacteria and the like infected by the hands in subsequent activities can pollute the hands again.

Disclosure of Invention

The invention aims to provide a novel no-clean hand sanitizer capable of continuously sterilizing so as to solve the problems in the background technology.

In order to achieve the purpose, the invention provides the following technical scheme: a novel no-clean hand sanitizer capable of continuously sterilizing is characterized in that: the raw materials comprise 14.7-26.7% of deionized water, 65-75% of ethanol (95%), 2-5% of glycerin (medical grade), 1-4% of propylene glycol, 4-6% of UIV2000 nano silver ion solution and 4-6% of carbomer U20: 0.3 to 0.4 percent of triethanolamine, 0.15 to 0.2 percent of tea tree essential oil, 0.2 to 0.8 percent of aloe extract and 0.5 to 1.5 percent of aloe extract;

the production process comprises the following steps:

s1, blending and taking U20, and pre-dispersing the U20 into glycerol;

s2, adding deionized water, heating to 80 ℃, and fully stirring;

s3, homogenizing and stirring at 12000RPM for 3 min;

s4, adding absolute ethyl alcohol, and fully stirring and mixing;

s5, mixing triethanolamine and water, 1: 5, after mixing, gradually adding a small amount of the mixture into the main system, and continuously stirring;

s6, observing that the viscosity of the main system meets the requirement, the material body is clear and transparent, stopping adding the mixed solution in the previous step, continuously stirring for 10min, and cooling the material body to the normal temperature;

s7, sequentially adding UIV2000 silver ion solution, tea tree essential oil and aloe extract, and mixing.

Preferably, the raw materials comprise 14.7 percent of deionized water, 65 percent of ethanol (95%), 2 percent of glycerin (medical grade), 1 percent of propylene glycol, 4 percent of UIV2000 nano silver ion solution and 4 percent of carbomer U20: 0.3 percent, 0.15 percent of triethanolamine, 0.2 percent of tea tree essential oil and 0.5 percent of aloe extract.

Preferably, the raw materials comprise 18.7 percent of deionized water, 69 percent of ethanol (95%), 3 percent of glycerin (medical grade), 2 percent of propylene glycol, 4.6 percent of UIV2000 nano silver ion solution, and 4.78 percent of carbomer U20: 0.33 percent, 0.17 percent of triethanolamine, 0.4 percent of tea tree essential oil and 0.8 percent of aloe extract.

Preferably, the raw materials comprise 22.7 percent of deionized water, 72 percent of ethanol (95%), 4 percent of glycerin (medical grade), 3 percent of propylene glycol, 5.3 percent of UIV2000 nano silver ion solution, and 5.3 percent of carbomer U20: 0.36 percent, 0.19 percent of triethanolamine, 0.6 percent of tea tree essential oil and 1.2 percent of aloe extract.

Preferably, the raw materials comprise 26.7 percent of deionized water, 75 percent of ethanol (95%), 5 percent of glycerin (medical grade), 4 percent of propylene glycol, 6 percent of UIV2000 nano silver ion solution, and carbomer U20: 0.4 percent of triethanolamine, 0.2 percent of tea tree essential oil and 1.5 percent of aloe extract.

Preferably, the action time of the hand sanitizer is 2-20 min.

Compared with the prior art, the invention has the beneficial effects that:

1. the invention has the technical key points that the specific silver ion concentration can continuously inhibit bacteria and has no influence on hands, and the system stability of the silver ions can be ensured simultaneously by matching with other additives, thereby playing the roles of disinfecting and protecting the hands.

Drawings

FIG. 1 is a process flow diagram of the present invention.

Detailed Description

The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.

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