CN101054482A - Surface modifying method for natural brucite ultra thin powder and application thereof - Google Patents

Surface modifying method for natural brucite ultra thin powder and application thereof Download PDF

Info

Publication number
CN101054482A
CN101054482A CN 200610039737 CN200610039737A CN101054482A CN 101054482 A CN101054482 A CN 101054482A CN 200610039737 CN200610039737 CN 200610039737 CN 200610039737 A CN200610039737 A CN 200610039737A CN 101054482 A CN101054482 A CN 101054482A
Authority
CN
China
Prior art keywords
powder
natural brucite
gained
surface modifying
brucite
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.)
Pending
Application number
CN 200610039737
Other languages
Chinese (zh)
Inventor
秦建国
汤秀英
吴振洲
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.)
NANTONG DONGZHOU MAGNESIUM CHEMICAL INDUSTRY MATERIAL Co Ltd
Original Assignee
NANTONG DONGZHOU MAGNESIUM CHEMICAL INDUSTRY MATERIAL 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 NANTONG DONGZHOU MAGNESIUM CHEMICAL INDUSTRY MATERIAL Co Ltd filed Critical NANTONG DONGZHOU MAGNESIUM CHEMICAL INDUSTRY MATERIAL Co Ltd
Priority to CN 200610039737 priority Critical patent/CN101054482A/en
Publication of CN101054482A publication Critical patent/CN101054482A/en
Pending legal-status Critical Current

Links

Abstract

The invention relates to a surface modify method of a natural brucite ultra fine powder, comprising: making the natural brucite pretreat, break up, abrade, grind in the gas flow disintegrator, adding the compound coupling agent in the anhydrous medium, activating and modifying on the continuous surface modifying machine. The produced natural brucite ultra fine powder has a high activation index and has an improved flame retardancy and mechanical performance as flame retardant after surface modifying treatment to the powder lot with compound coupling agent. The invention has a continuous production process and increased production efficiency after the activating and modifying treatment on the continuous surface modifying machine.

Description

The surface modifying method of natural brucite ultra thin powder and application thereof
Technical field
The present invention relates to a kind of process for modifying surface of environmental-protection flame-retardant compound, specifically a kind of surface modifying method of natural brucite ultra thin powder and application thereof.
Background technology
Magnesium hydroxide as a kind of nontoxic, fire-retardant, press down cigarette, heat-stable halogen-free inorganic flame retardant, present good development prospect at home and abroad, just progressively replace aluminium hydroxide.Brucite is highly purified hydrogeneous magnesian ore, is the desirable feedstock of inorganic combustion inhibitor, because this is as inorganics, there is polarity on the surface, and is relatively poor with superpolymer base-material consistency.For the mechanical property that guarantees to add the back matrix material in the scope of application, must carry out modification to its surface and handle.Dry method modification saves the filtration and the drying and other steps of back owing to do not add water medium, and cost is low, is extensively adopted by the powder industry.CN1374352A discloses " surface modification of brucite powder, wollastonite powder and method ", and this application adopts solid coupling agent stearic acid, aluminic acid ester and liquid coupling agent titanic acid ester, silane to the brucite powder modification.Owing to adopt single coupling agent, and use slow, the inefficient kneader of rotating speed as modified device, and handle powder at normal temperatures, thereby make modified effect not good enough, in addition, this patent does not report that activation index uses the data of back flame retardant resistance and mechanical property aspect plastics.
Summary of the invention
The objective of the invention is to provide with the high-purity water magnesite is raw material, adopts composite coupler, finishes the surface modification process on the continuous modification machine efficiently, makes the powder of making have the surface modifying method of the high a kind of natural brucite ultra thin powder of activation index.
Another object of the present invention is to provide ultrafine powder that above-mentioned surface modifying method makes when making plastics such as PE, PP, ABS, polycarbonate, the application method that flame retardant properties, mechanical property are obviously improved.
According to the foregoing invention purpose, the surface modifying method of natural brucite ultra thin powder of the present invention comprises the following steps:
1. natural brucite is carried out pre-treatment;
2. pretreated natural brucite is carried out fragmentation;
3. with step 2. the material of gained send into pulverizer and carry out grinding, the material fineness is 300~500 orders;
4. with step 3. the powder of gained send into micronizer mill and be ground to 1250~3000 orders;
5. with step 4. the gained powder on continous way surface modification machine, carry out activation modification and handle adding composite coupler under the anhydrous medium, temperature is 80~120 ℃, the treatment time is 15~30 minutes;
6. with 5. diffusing, the cooling of gained material economy-combat of step, make the natural brucite ultra thin powder that surface modification is crossed.
The step 5. composite coupler of described adding is made up of the solid silicon compound that accounts for powder weight 1%~3%, 1%~3% titanate coupling agent, the saturated hydrocarbon solvent that 2%~3% boiling point is higher than 200 ℃.
The halogen-free flame-retardance of the ultrafine powder that described surface modifying method makes when PE, PP, ABS, polycarbonate plastic application can reach the UL94V-0 level, the mechanical property excellence.
Compared with the prior art the present invention has following advantage:
(1) owing to adopts composite coupler that powder is carried out surface modification, carrying out modification with single coupling agent compares, make the natural brucite ultra thin powder activation index height of producing, when making product be used as fire retardant, flame retardant properties, mechanical property obviously improve, aspect the low-smoke non-halogen flame-retardant of plastics such as PE, PP, ABS, polycarbonate, use, demonstrate obvious advantage.
(2) owing to take on continous way surface modification machine, to carry out the activation modification processing, handle continuously, improved production efficiency greatly thereby make to produce.
(3) owing to take dry method that natural brucite ultra thin powder is carried out surface modification treatment, compare, saved filtration, drying and other steps, make production cost low with the wet method surface modification technology.
Embodiment
Below in conjunction with embodiment the present invention is further described:
Embodiment one:
The surface modifying method of natural brucite ultra thin powder of the present invention comprises the following steps:
1. the natural brucite with capacity carries out the picking pre-treatment, makes brucite material composition content: MgO 〉=66%, Fe 2O 3≤ 0.5%, SiO 2≤ 0.5%;
2. the pretreated natural brucite with capacity carries out Hubei Province formula crusher machine;
3. with step 2. the material of gained send into Raymond machine and carry out grinding, the material fineness is 325 orders;
4. with step 3. the powder of gained send into micronizer mill and grind carefully to 1250 orders;
5. get 4. gained powder 200kg of step, send on the continous way surface modification machine, 100 ℃ of preheating dehydrations, make powder be in no aqueous condition, add continuously solid silicon compound 6kg, atomizing sprays into the mixed solution that titanate coupling agent 6kg and 6kg boiling point are higher than 200 ℃ saturated hydrocarbon solvent continuously again, carries out the activation modification processing, temperature is controlled at 120 ℃, and the treatment time is 20 minutes;
6. with 5. diffusing, the cooling of gained material economy-combat of step, make the natural brucite ultra thin powder that surface modification is crossed, gained powder activation index is 99% after testing.
Get 100 parts and 100 parts PE of brucite ultrafine powder weight, 10 parts of phosphorus flame retardants, 6 parts of modifying agents of processing, 0.2 part in oxidation inhibitor that aforesaid method makes, mixing 8 minutes, temperature was controlled at 100 ℃; 130 ℃ of temperature, pressure is 12MPa state compressing tablet again.Product oxygen index after tested is 40%, and anti-to stretch intensity be 10MPa, and elongation at break is 120%, notched Izod impact strength 12kg/m 2
Embodiment two:
The surface modifying method of the natural brucite ultra thin powder of present embodiment comprises the following steps:
1. the natural brucite with capacity carries out the picking pre-treatment, makes brucite material composition content: MgO 〉=66%, Fe 2O 3≤ 0.5%, SiO 2≤ 0.5%;
2. the pretreated natural brucite with capacity carries out fragmentation;
3. with step 2. the material of gained send into pulverizer and carry out grinding, the material fineness is 500 orders;
4. with step 3. the powder of gained send into micronizer mill and be ground to 3000 orders;
5. get 4. gained powder 200kg of step, send on the continous way surface modification machine, 100 ℃ of thermal dehydrations, make powder be in no aqueous condition, add continuously solid silicon compound 2kg, atomizing sprays into the mixed solution that titanate coupling agent 2kg and 4kg boiling point are higher than 200 ℃ saturated hydrocarbon solvent continuously again, carries out the activation modification processing, temperature is controlled at 80 ℃, and the treatment time is 30 minutes;
6. with 5. diffusing, the cooling of gained material economy-combat of step, make the natural brucite ultra thin powder that surface modification is crossed, gained powder activation index is 98% after testing.
Get 80 parts and 100 parts PP of brucite ultrafine powder weight, 8 parts of phosphorus flame retardants, 7 parts of modifying agents of processing, 0.3 part in oxidation inhibitor that aforesaid method makes, mixing 10 minutes, temperature was controlled at 150 ℃; 190 ℃ of temperature, pressure is 12MPa state compressing tablet again.Product oxygen index after tested is 33%, and anti-to stretch intensity be 20MPa, and elongation at break is 40%, notched Izod impact strength 28kg/m 2
In sum, the ultrafine powder that surface modifying method of the present invention makes, when using on PE, PP, ABS, polycarbonate plastic, halogen-free flame-retardance can reach the UL94V-0 level, and mechanical property is obviously excellent.

Claims (3)

1, the surface modifying method of natural brucite ultra thin powder is characterized in that: comprise the following steps:
1. natural brucite is carried out pre-treatment;
2. pretreated natural brucite is carried out fragmentation;
3. with step 2. the material of gained send into pulverizer and carry out grinding, the material fineness is 300~500 orders;
4. with step 3. the powder of gained send into micronizer mill and be ground to 1250~3000 orders;
5. with step 4. the gained powder on continous way surface modification machine, carry out activation modification and handle adding composite coupler under the anhydrous medium, temperature is 80~120 ℃, the treatment time is 15~30 minutes;
6. with 5. diffusing, the cooling of gained material economy-combat of step, make the natural brucite ultra thin powder that surface modification is crossed.
2, the surface modifying method of natural brucite ultra thin powder as claimed in claim 1 is characterized in that: the step 5. composite coupler of described adding is made up of the solid silicon compound that accounts for powder weight 1%~3%, 1%~3% titanate coupling agent, the saturated hydrocarbon solvent that 2%~3% boiling point is higher than 200 ℃.
3, the application of surface modifying method gained powder according to claim 1 is characterized in that: the halogen-free flame-retardance of the ultrafine powder that makes when PE, PP, ABS, polycarbonate plastic application can reach the UL94V-0 level, the mechanical property excellence.
CN 200610039737 2006-04-14 2006-04-14 Surface modifying method for natural brucite ultra thin powder and application thereof Pending CN101054482A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 200610039737 CN101054482A (en) 2006-04-14 2006-04-14 Surface modifying method for natural brucite ultra thin powder and application thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 200610039737 CN101054482A (en) 2006-04-14 2006-04-14 Surface modifying method for natural brucite ultra thin powder and application thereof

Publications (1)

Publication Number Publication Date
CN101054482A true CN101054482A (en) 2007-10-17

Family

ID=38794543

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 200610039737 Pending CN101054482A (en) 2006-04-14 2006-04-14 Surface modifying method for natural brucite ultra thin powder and application thereof

Country Status (1)

Country Link
CN (1) CN101054482A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101538419B (en) * 2009-04-09 2012-07-04 池州灵芝化建材料科技有限公司 Process for preparing brucite inorganic flame retardant
CN103265826A (en) * 2013-06-13 2013-08-28 苏州新区华士达工程塑胶有限公司 Inorganic flame retardant surface modification method
CN103923491A (en) * 2014-04-11 2014-07-16 河北科技大学 Special magnesium oxide for glass reinforced plastics produced with unsaturated polyester resins and preparation method thereof
CN105037810A (en) * 2015-07-23 2015-11-11 北京理工大学 Method for preparing alginate modified brucite composite flame retardant
CN105733089A (en) * 2014-12-06 2016-07-06 沈阳工业大学 Brucite composite flame-retardant polypropylene material and preparation method thereof
CN106543773A (en) * 2016-11-01 2017-03-29 蚌埠硅基材料产业技术研究院有限公司 The scale surface treatment method of the superfine quartz powder of median≤2 μm
CN106829994A (en) * 2017-03-09 2017-06-13 金华市欣生沸石开发有限公司 Zeolite powder production line and production technology
CN112300602A (en) * 2020-10-29 2021-02-02 北京化工大学 Modification method of inorganic filler

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101538419B (en) * 2009-04-09 2012-07-04 池州灵芝化建材料科技有限公司 Process for preparing brucite inorganic flame retardant
CN103265826A (en) * 2013-06-13 2013-08-28 苏州新区华士达工程塑胶有限公司 Inorganic flame retardant surface modification method
CN103923491A (en) * 2014-04-11 2014-07-16 河北科技大学 Special magnesium oxide for glass reinforced plastics produced with unsaturated polyester resins and preparation method thereof
CN103923491B (en) * 2014-04-11 2016-08-17 河北科技大学 A kind of unsaturated polyester resin produces fiberglass special magnesium oxide and preparation method thereof
CN105733089A (en) * 2014-12-06 2016-07-06 沈阳工业大学 Brucite composite flame-retardant polypropylene material and preparation method thereof
CN105037810A (en) * 2015-07-23 2015-11-11 北京理工大学 Method for preparing alginate modified brucite composite flame retardant
CN105037810B (en) * 2015-07-23 2017-08-22 北京理工大学 A kind of alginate is modified the preparation method of shepardite composite flame-retardant agent
CN106543773A (en) * 2016-11-01 2017-03-29 蚌埠硅基材料产业技术研究院有限公司 The scale surface treatment method of the superfine quartz powder of median≤2 μm
CN106829994A (en) * 2017-03-09 2017-06-13 金华市欣生沸石开发有限公司 Zeolite powder production line and production technology
CN106829994B (en) * 2017-03-09 2019-05-28 金华市欣生沸石开发有限公司 Zeolite powder production line and production technology
CN112300602A (en) * 2020-10-29 2021-02-02 北京化工大学 Modification method of inorganic filler

Similar Documents

Publication Publication Date Title
CN101054482A (en) Surface modifying method for natural brucite ultra thin powder and application thereof
Shi et al. Synthesis of DOPO-HQ-functionalized graphene oxide as a novel and efficient flame retardant and its application on polylactic acid: Thermal property, flame retardancy, and mechanical performance
Chen et al. Simultaneous production and functionalization of boron nitride nanosheets by sugar‐assisted mechanochemical exfoliation
Xu et al. Fabrication of green alginate-based and layered double hydroxides flame retardant for enhancing the fire retardancy properties of polypropylene
Gao et al. Nanocomposite based on poly (acrylic acid)/attapulgite towards flame retardant of cotton fabrics
Cai et al. A novel strategy to simultaneously electrochemically prepare and functionalize graphene with a multifunctional flame retardant
Qu et al. Facile preparation of BP-MoS2/GO composite films with excellent flame retardancy and ultrasensitive response for smart fire alarm
Yu et al. Interface nanoengineering of a core-shell structured biobased fire retardant for fire-retarding polylactide with enhanced toughness and UV protection
Gong et al. Organic-inorganic hybrid engineering MXene derivatives for fire resistant epoxy resins with superior smoke suppression
Xu et al. The effect of ammonium polyphosphate on the mechanism of phosphorous-containing hydrotalcite synergism of flame retardation of polypropylene
Yam et al. Recycling of magnesium waste into magnesium hydroxide aerogels
CN101760011B (en) Method for preparing nylon 6/graphite oxide nanocomposite
CN109517220B (en) Preparation method of nano tin-based intumescent flame retardant
Nahrawy et al. Uniformly embedded cellulose/polypyrrole-TiO 2 composite in sol-gel sodium silicate nanoparticles: structural and dielectric properties
Ye et al. Durable flame-retardant, strong and tough epoxy resins with well-preserved thermal and optical properties via introducing a bio-based, phosphorus-phosphorus, hyperbranched oligomer
Wang et al. In-situ preparation of layered zinc N, N’-piperazine (bismethylene phosphonate) functionalizing reduced graphene oxide for epoxy resin with reduced fire hazards and improved thermal/mechanical properties
Cai et al. Recyclable and removable functionalization based on Diels-Alder reaction of black phosphorous nanosheets and its dehydration carbonization in fire safety improvement of polymer composites
CN114410128A (en) Magnesium hydroxide ultra-fining and surface modification method and application thereof
Guo et al. Simultaneous exfoliation and functionalization of black phosphorus by sucrose-assisted ball milling with NMP intercalating and preparation of flame retardant polyvinyl alcohol film
Wang et al. Effect of modified hydrotalcites on flame retardancy and physical properties of paper
Song et al. Chitosan-regulated inorganic oxyacid salt flame retardants: preparation and application in PVC composites
CN111019123A (en) Method for flame-retardant modification of polyamide 56 by biomimetic modification of Lehm stone/graphene oxide nano composite material
Xu et al. Nickel-based metal—organic framework-derived whisker-shaped nickel phyllosilicate toward efficiently enhanced mechanical, flammable and tribological properties of epoxy nanocomposites
Wang et al. Surface modification of cellulose microcrystalline with aluminate coupling agent and its effects on flame retardant and mechanical properties of epoxy resin
CN1332116A (en) Homogeneous fluid process of preparing nanometer magnesium hydroxide

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication