CN104263035A - Anti-bacterial color paste material and preparation method thereof - Google Patents

Anti-bacterial color paste material and preparation method thereof Download PDF

Info

Publication number
CN104263035A
CN104263035A CN201410491908.7A CN201410491908A CN104263035A CN 104263035 A CN104263035 A CN 104263035A CN 201410491908 A CN201410491908 A CN 201410491908A CN 104263035 A CN104263035 A CN 104263035A
Authority
CN
China
Prior art keywords
mill base
antibacterial
base material
parts
mixture
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN201410491908.7A
Other languages
Chinese (zh)
Other versions
CN104263035B (en
Inventor
李冰心
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SUZHOU BINGXIN STATIONERY Co Ltd
Original Assignee
SUZHOU BINGXIN STATIONERY Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by SUZHOU BINGXIN STATIONERY Co Ltd filed Critical SUZHOU BINGXIN STATIONERY Co Ltd
Priority to CN201410491908.7A priority Critical patent/CN104263035B/en
Publication of CN104263035A publication Critical patent/CN104263035A/en
Application granted granted Critical
Publication of CN104263035B publication Critical patent/CN104263035B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The invention discloses an anti-bacterial color paste material and a preparation method thereof. The anti-bacterial color paste material is prepared from the following components in parts by weight: 20-40 parts of methyl acrylate, 10-20 parts of dipropylene glycol dimethyl ether, 10-15 parts of chitosan, 3-12 parts of hydroxyethylmethylcellulose, 5-8 parts of polymethyl acrylamide propyl trimethyl ammonium chloride, 0.8-2 parts of octyl isothiazolone, 0.8-1.5 parts of phenoxyethanol and 0.5-1 part of a pigment. The color paste material prepared by using the method disclosed by the invention has good dispersion effects and good anti-bacterial performance, and can be used as the paste materials of the surfaces of various stationery.

Description

A kind of antibacterial mill base material and preparation method thereof
Technical field
The invention belongs to mill base Material Field, particularly antibacterial mill base material of one and preparation method thereof.
Background technology
In daily life, mill base is that the life of people adds color, brings the visual effect of more U.S.s, is the requisite material of decoration.Along with the development of mill base material, the demand for the mill base with anti-microbial property is also increasing, particularly in each field directly contacted with human skin, particularly pays close attention to especially, so-called antibacterial, refers to the Growth and reproduction of anti-bacteria within a certain period of time.In order to make mill base have certain anti-microbial effect, often needing in formula, add corresponding antiseptic-germicide, making mill base have good antibacterial.But along with adding of antiseptic-germicide, what bring is the variation of consistency between each component in mill base thereupon, mill base dispersiveness reduces, homogeneity is deteriorated.
Summary of the invention
For above-mentioned demand, the object of the present invention is to provide a kind of antibacterial mill base material and preparation method thereof, the mill base material obtained by present method not only has good dispersion effect, and has good antimicrobial property.
Object of the present invention can be achieved through the following technical solutions:
A kind of antibacterial mill base material, be made up of the component comprising following weight part:
Methyl acrylate 20-40 part,
Dimethyl ether 10-20 part,
Chitin 10-15 part,
Hydroxyethylmethyl-cellulose 3-12 part,
PMAm hydroxypropyltrimonium chloride 5-8 part,
N-octyl-isothiazolin ketone 0.8-2 part,
Phenoxyethanol 0.8-1.5 part,
Pigment 0.5-1 part.
Described pigment is titanium white or cadmium yellow.
Described Phenoxyethanol is 1 weight part.
A preparation method for antibacterial mill base material, the method comprises the following steps:
(1) methyl acrylate 20-40 part, dimethyl ether 10-20 part, hydroxyethylmethyl-cellulose 3-12 part, PMAm hydroxypropyltrimonium chloride 5-8 part and n-octyl-isothiazolin ketone 0.8-2 part is taken, add in high pressure homogenizer, reaction 1-2 hour, obtains mixture A;
(2) in the mixture of step 1, add pigment 0.5-1 part, Phenoxyethanol 0.8-1.5 part and chitin 10-15 part successively, at 65-75 DEG C, stir 10-20 minute, obtain mixture B;
(3) add 1M sodium carbonate adjust ph to 7.8 by the mixture B of step 2, deaeration 1 hour in vacuum defoamation machine, obtains antibacterial mill base material.
The reaction pressure of described step 1 mesohigh clarifixator is 12Mpa, and temperature of reaction is 50-65 DEG C.
The present invention compared with prior art, its beneficial effect is: in the present invention, owing to adding Phenoxyethanol, mill base is made to have good anti-microbial property, simultaneously before adding antimicrobial component Phenoxyethanol, add homogeneity and tack that PMAm hydroxypropyltrimonium chloride improves mill base.Present invention adds chitin and n-octyl-isothiazolin ketone, make pigment have good dispersiveness in whole system, mill base material of the present invention can be used for all kinds of stationery surface, while being rich in certain color, have good antibacterial effect.
Embodiment
Below in conjunction with embodiment, the present invention is further illustrated.
Embodiment 1
(1) methyl acrylate 20kg, dimethyl ether 20kg, hydroxyethylmethyl-cellulose 3kg, PMAm hydroxypropyltrimonium chloride 5kg and n-octyl-isothiazolin ketone 0.8kg is taken, add that reaction pressure is 12Mpa, temperature is in the high pressure homogenizer of 50 DEG C, react 1 hour, obtain mixture A;
(2) in the mixture of step 1, add cadmium yellow 0.5kg, Phenoxyethanol 0.8kg and chitin 10kg successively, at 65 DEG C, stir 15 minutes, obtain mixture B;
(3) add 1M sodium carbonate adjust ph to 7.8 by the mixture B of step 2, deaeration 1 hour in vacuum defoamation machine, obtains antibacterial mill base material.
Obtained antibacterial mill base coated materials is in frosting, and the performance test results obtained is as shown in table 1.
Embodiment 2
(1) methyl acrylate 30kg, dimethyl ether 10kg, hydroxyethylmethyl-cellulose 10kg, PMAm hydroxypropyltrimonium chloride 8 kg and n-octyl-isothiazolin ketone 1kg is taken, add that reaction pressure is 12Mpa, temperature is in the high pressure homogenizer of 65 DEG C, react 1 hour, obtain mixture A;
(2) in the mixture of step 1, add cadmium yellow 1 kg, Phenoxyethanol 1.5 kg and chitin 15 kg successively, at 75 DEG C, stir 10 minutes, obtain mixture B;
(3) add 1M sodium carbonate adjust ph to 7.8 by the mixture B of step 2, deaeration 1 hour in vacuum defoamation machine, obtains antibacterial mill base material.
Obtained antibacterial mill base coated materials is in frosting, and the performance test results obtained is as shown in table 1.
Embodiment 3
(1) methyl acrylate 40kg, dimethyl ether 15kg, hydroxyethylmethyl-cellulose 8kg, PMAm hydroxypropyltrimonium chloride 6kg and n-octyl-isothiazolin ketone 2 kg is taken, add that reaction pressure is 12Mpa, temperature is in the high pressure homogenizer of 60 DEG C, react 2 hours, obtain mixture A;
(2) in the mixture of step 1, add cadmium yellow 0.8kg, benzene oxygen second 1 kg and chitin 12kg successively, at 70 DEG C, stir 15 minutes, obtain mixture B;
(3) add 1M sodium carbonate adjust ph to 7.8 by the mixture B of step 2, deaeration 1 hour in vacuum defoamation machine, obtains antibacterial mill base material.
Obtained antibacterial mill base coated materials is in frosting, and the performance test results obtained is as shown in table 1.
Embodiment 4
(1) methyl acrylate 35kg, dimethyl ether 10kg, hydroxyethylmethyl-cellulose 12 kg, PMAm hydroxypropyltrimonium chloride 5kg and n-octyl-isothiazolin ketone 1kg is taken, add that reaction pressure is 12Mpa, temperature is in the high pressure homogenizer of 50 DEG C, react 1 hour, obtain mixture A;
(2) in the mixture of step 1, add cadmium yellow 1 kg, Phenoxyethanol 1.2kg and chitin 15 kg successively, at 65 DEG C, stir 10 minutes, obtain mixture B;
(3) add 1M sodium carbonate adjust ph to 7.8 by the mixture B of step 2, deaeration 1 hour in vacuum defoamation machine, obtains antibacterial mill base material.
Table 1
Test event Embodiment 1 Embodiment 2 Embodiment 3
Fineness < 4 microns < 4 microns < 4 microns
The colony number sum of streptococcus aureus in every ml physiological saline Be less than 500 Be less than 500 Be less than 500
Antibacterial mill base in embodiment 1-3 is sprayed in stationery surface respectively, tests after dry.
Testing method: be positioned over by the stationery of the mill base scribbled in embodiment 1-3 in air after 24 hours, put into the physiological saline of 50 milliliters respectively, survey its colony number, test result is in table 1.
Contrast sample testing method, be positioned over by common stationery in air after 24 hours, put into the physiological saline of 50 milliliters, survey its colony number, test result is in table 1.
The invention is not restricted to embodiment here, those skilled in the art, according to announcement of the present invention, do not depart from improvement that scope makes and amendment all should within protection scope of the present invention.

Claims (5)

1. an antibacterial mill base material, is characterized in that, is made up of the component comprising following weight part:
Methyl acrylate 20-40 part,
Dimethyl ether 10-20 part,
Chitin 10-15 part,
Hydroxyethylmethyl-cellulose 3-12 part,
PMAm hydroxypropyltrimonium chloride 5-8 part,
N-octyl-isothiazolin ketone 0.8-2 part,
Phenoxyethanol 0.8-1.5 part,
Pigment 0.5-1 part.
2. antibacterial mill base material according to claim 1, is characterized in that, described pigment is titanium white or cadmium yellow.
3. antibacterial mill base material according to claim 1, is characterized in that, described Phenoxyethanol is 1 weight part.
4. a preparation method for antibacterial mill base material, it is characterized in that, the method comprises the following steps:
(1) methyl acrylate 20-40 part, dimethyl ether 10-20 part, hydroxyethylmethyl-cellulose 3-12 part, PMAm hydroxypropyltrimonium chloride 5-8 part and n-octyl-isothiazolin ketone 0.8-2 part is taken, add in high pressure homogenizer, reaction 1-2 hour, obtains mixture A;
(2) in the mixture of step 1, add pigment 0.5-1 part, Phenoxyethanol 0.8-1.5 part and chitin 10-15 part successively, at 65-75 DEG C, stir 10-20 minute, obtain mixture B;
(3) add 1M sodium carbonate adjust ph to 7.8 by the mixture B of step 2, deaeration 1 hour in vacuum defoamation machine, obtains antibacterial mill base material.
5. the preparation method of antibacterial mill base material according to claim 4, is characterized in that, the reaction pressure of described step 1 mesohigh clarifixator is 12Mpa, and temperature of reaction is 50-65 DEG C.
CN201410491908.7A 2014-09-24 2014-09-24 A kind of antibacterial mill base material and preparation method thereof Active CN104263035B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201410491908.7A CN104263035B (en) 2014-09-24 2014-09-24 A kind of antibacterial mill base material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201410491908.7A CN104263035B (en) 2014-09-24 2014-09-24 A kind of antibacterial mill base material and preparation method thereof

Publications (2)

Publication Number Publication Date
CN104263035A true CN104263035A (en) 2015-01-07
CN104263035B CN104263035B (en) 2016-08-31

Family

ID=52154626

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201410491908.7A Active CN104263035B (en) 2014-09-24 2014-09-24 A kind of antibacterial mill base material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN104263035B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105803830A (en) * 2016-04-05 2016-07-27 吴江市林旺纺织厂 Color paste material for textiles and preparation method of color paste material
CN108797920A (en) * 2018-06-15 2018-11-13 福建戎堃科技有限公司 A kind of production method of nano antibacterial, moldproof decorative paste paperboard

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5792793A (en) * 1993-11-05 1998-08-11 Meiji Milk Products Co., Ltd. Antibacterial, antifungal and antiviral agent
CN102372949A (en) * 2010-08-09 2012-03-14 曾炽涛 Aqueous pigment slurry and preparation method thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5792793A (en) * 1993-11-05 1998-08-11 Meiji Milk Products Co., Ltd. Antibacterial, antifungal and antiviral agent
CN102372949A (en) * 2010-08-09 2012-03-14 曾炽涛 Aqueous pigment slurry and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105803830A (en) * 2016-04-05 2016-07-27 吴江市林旺纺织厂 Color paste material for textiles and preparation method of color paste material
CN108797920A (en) * 2018-06-15 2018-11-13 福建戎堃科技有限公司 A kind of production method of nano antibacterial, moldproof decorative paste paperboard

Also Published As

Publication number Publication date
CN104263035B (en) 2016-08-31

Similar Documents

Publication Publication Date Title
CN104017446B (en) A kind of environmental protection coating material
WO2013016257A8 (en) Botanical antioxidant compositions and methods of preparation and use thereof
CN104031442B (en) Antimicrobial preservative coating and preparation method thereof
BRPI0712631A8 (en) compounds, processes for the preparation of a compound, pharmaceutical composition, use of a compound and combinations
WO2009122436A3 (en) An improved process for the preparation of morphinane analogues
WO2008087605A3 (en) Composition and method of stabilized sensitive ingredient
WO2006127810A8 (en) Bacterial cellulose-containing formulations and method of producing effective bacterial cellulose-containing formulations
CN104263035A (en) Anti-bacterial color paste material and preparation method thereof
CN102229771A (en) Diatomaceous earth active paint and preparation method thereof
CN101921534A (en) Antibacterial powder coating for radiator
CN104877495A (en) Anti-bacteria coating
PH12020551035A1 (en) Novel anthranilamides, their use as insecticide and processes for preparing the same
CN105062258A (en) Fireproof coating
CN103222477B (en) Silver ion inorganic antiseptic and melamine resin and impregnated paper prepared by same
WO2013128271A3 (en) Process for the preparation of cement, mortars, concrete compositions containing calcium carbonate - based filler(s) (pre) -treated with ultrafine (uf) filler(s), compositions and cement products obtained and their applications
CN106223017A (en) A kind of green nano-antibacterial high pressure permeability environment protection novel
CN104263151A (en) Acrylic orange-figured paint and preparation method thereof
WO2008079963A3 (en) Pharmaceutical compositions comprising ionic complexes of active pharmaceutical ingredients
CN103239744A (en) Deodorizing fragrance bag for refrigerator
CN107938437A (en) A kind of environmental protection wall clothing
CN104231755B (en) A kind of Graphene modification mill base material and preparation method thereof
CN103866644B (en) A kind of antiseptic and preparation method thereof
CN105778613A (en) Special antioxidant for paint
CN105755812A (en) Additive for spinning sizing agent and preparation method thereof
CN103410016B (en) Green textile pigment with good stability

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant