CN103613961B - A kind ofly reduce water-soluble inorganic oxygenant or the water-soluble inorganic salt method at oil-soluble material median surface tension force - Google Patents

A kind ofly reduce water-soluble inorganic oxygenant or the water-soluble inorganic salt method at oil-soluble material median surface tension force Download PDF

Info

Publication number
CN103613961B
CN103613961B CN201310646408.1A CN201310646408A CN103613961B CN 103613961 B CN103613961 B CN 103613961B CN 201310646408 A CN201310646408 A CN 201310646408A CN 103613961 B CN103613961 B CN 103613961B
Authority
CN
China
Prior art keywords
water
soluble inorganic
soluble
inorganic salt
oxygenant
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.)
Expired - Fee Related
Application number
CN201310646408.1A
Other languages
Chinese (zh)
Other versions
CN103613961A (en
Inventor
刘天晴
左明明
郭静
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.)
Yangzhou University
Original Assignee
Yangzhou University
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 Yangzhou University filed Critical Yangzhou University
Priority to CN201310646408.1A priority Critical patent/CN103613961B/en
Publication of CN103613961A publication Critical patent/CN103613961A/en
Application granted granted Critical
Publication of CN103613961B publication Critical patent/CN103613961B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Cosmetics (AREA)

Abstract

Reduce water-soluble inorganic oxygenant or water-soluble inorganic salt in a method for oil-soluble material median surface tension force, belong to novel material, technical field of chemistry and chemical engineering.First stearic acid and sodium stearate are dissolved in 1,2-PD, form mixing solutions; Then butyl (tetra) titanate and ethanol are added mixing solutions, react to after terminating under the envrionment temperature of 105 DEG C, temperature of reaction system is down to 90 DEG C, add water-soluble inorganic oxygenant or water-soluble inorganic salt again, react under agitation condition to terminating, through cooling, water-soluble inorganic oxygenant or the water-soluble inorganic salt of interfacial tension must be reduced.The present invention effectively can reduce the interfacial tension of water-soluble inorganic oxygenant or water-soluble inorganic salt and oil-soluble material, can improve the encapsulation rate of oil-soluble material to water-soluble inorganic oxygenant or water-soluble inorganic salt.

Description

A kind ofly reduce water-soluble inorganic oxygenant or the water-soluble inorganic salt method at oil-soluble material median surface tension force
Technical field
The invention belongs to novel material, technical field of chemistry and chemical engineering.
Background technology
Water-soluble inorganic oxygenant or water-soluble inorganic salt (as cerium oxide, sodium peroxide, Sodium Persulfate, ammonium persulphate, Potassium Persulphate etc.) are widely used in the manufacture of aniline dyestuff, the oxidation color development of vat pigment, metal finishing, organic synthesis, the initiation of polymer polymerization, the decolouring of oil and bleaching, become in the field such as ripener, oil production of the washing that loses yeast and deodorization, wheat.But above-mentioned water-soluble inorganic oxygenant or water-soluble inorganic salt extremely unstable at ambient temperature, as being subject to moisture in air to its deliquescence caking, easily decomposes etc.
For solving the problem, now widely used technology is the lapping of isolating at the outside bag one deck of above-mentioned water-soluble inorganic oxygenant or water-soluble inorganic salt and external environment.Conventional lapping has the oil-soluble materials such as polystyrene, polyacrylonitrile, whiteruss.But these water-soluble inorganic oxygenants or water-soluble inorganic salt are hydrophilic, and above-mentioned all kinds of lapping belongs to oil loving, so be difficult to effectively both be combined.
Summary of the invention
The present invention seeks to propose a kind of method of reduction water-soluble inorganic salt at oil-soluble material median surface tension force improving water-soluble inorganic oxygenant or water-soluble inorganic salt encapsulation ratio.
Technical solution of the present invention is: be first dissolved in 1,2-PD by stearic acid and sodium stearate, forms mixing solutions; Then butyl (tetra) titanate and ethanol are added mixing solutions, react to after terminating under the envrionment temperature of 105 DEG C, temperature of reaction system is down to 90 DEG C, add water-soluble inorganic oxygenant or water-soluble inorganic salt again, react under agitation condition to terminating, through cooling, water-soluble inorganic oxygenant or the water-soluble inorganic salt of interfacial tension must be reduced.
The present invention carries out surface modification by above method to water-soluble inorganic oxygenant or water-soluble inorganic salt, the interfacial tension of effective reduction water-soluble inorganic oxygenant or water-soluble inorganic salt and oil-soluble material, adopt above reduce interfacial tension water-soluble inorganic oxygenant or water-soluble inorganic salt carry out parcel with lappings such as polystyrene, polyacrylonitrile, whiterusss again and process, just can be improved the encapsulation rate to 60% of oil-soluble material to water-soluble inorganic oxygenant or water-soluble inorganic salt.
Water-soluble inorganic oxygenant of the present invention or water-soluble inorganic salt and butyl (tetra) titanate, stearic acid, sodium stearate, 1,2-propylene glycol, ethanol account for 69% ~ 92%, 1% ~ 5%, 0.5% ~ 3%, 0.5% ~ 3%, 5% ~ 10% and 1% ~ 10% of the total mass that feeds intake respectively.
When the addition of above-mentioned each raw material is in the above scope limited, the interfacial tension of water-soluble inorganic oxygenant or water-soluble inorganic salt and oil-soluble material is minimum, and cost control is in lower scope.
Described water-soluble inorganic oxygenant or water-soluble inorganic salt are Sodium Persulfate, or cerium oxide, or sodium peroxide, or ammonium persulphate, or Potassium Persulphate.
Accompanying drawing explanation
Fig. 1 is the Sodium Persulfate scanning electron microscope (SEM) photograph of non-modified.
Fig. 2 is through modified Sodium Persulfate scanning electron microscope (SEM) photograph.
Fig. 3 is the Sodium Persulfate scanning electron microscope (SEM) photograph adopting polyacrylonitrile parcel non-modified.
Fig. 4 adopts polyacrylonitrile parcel through modified Sodium Persulfate scanning electron microscope (SEM) photograph.
Embodiment
One, preparation technology: accurately take the stearic acid of certain mass ratio and sodium stearate in there-necked flask, the 1,2-PD adding an amount makes it dissolve completely.Then a certain amount of butyl (tetra) titanate is slowly added and alcohol mixeding liquid reacted after 70 minutes under the condition of 105 DEG C, temperature of reaction is down to 90 DEG C, then add Sodium Persulfate or cerium oxide, sodium peroxide, ammonium persulphate, the Potassium Persulphate of respective quality, continue rapid stirring and react 2 hours.Refrigerating unit, receives sample.
Contribute to understanding the present invention by following specific embodiments, but do not limit content of the present invention.
Its per-cent (100%) that specifically each component accounts for the total mass that feeds intake in composition is:
Scheme 1: butyl (tetra) titanate 2%, stearic acid 2%, sodium stearate 0.5%, 1,2-propylene glycol 5%, ethanol 4%, all the other are Sodium Persulfate (or cerium oxide, sodium peroxide, ammonium persulphate, Potassium Persulphate).
Scheme 2: butyl (tetra) titanate 3%, stearic acid 3%, sodium stearate 1%, 1,2-propylene glycol 8%, ethanol 2%, all the other are Sodium Persulfate (or cerium oxide, sodium peroxide, ammonium persulphate, Potassium Persulphate).
Scheme 3: butyl (tetra) titanate 3.5%, stearic acid 2.5%, sodium stearate 1.5%, 1,2-propylene glycol 6%, ethanol 2%, all the other are Sodium Persulfate (or cerium oxide, sodium peroxide, ammonium persulphate, Potassium Persulphate).
Scheme 4: butyl (tetra) titanate 5%, stearic acid 3%, sodium stearate 3%, 1,2-propylene glycol 8%, ethanol 8%, all the other are Sodium Persulfate (or cerium oxide, sodium peroxide, ammonium persulphate, Potassium Persulphate).
Scheme 5: butyl (tetra) titanate 2.5%, stearic acid 2.5%, sodium stearate 1.5%, 1,2-propylene glycol 5%, ethanol 2%, all the other are Sodium Persulfate (or cerium oxide, sodium peroxide, ammonium persulphate, Potassium Persulphate).
Scheme 6: butyl (tetra) titanate 1%, stearic acid 0.5%, sodium stearate 0.5%, 1,2-propylene glycol 5%, ethanol 1%, all the other are Sodium Persulfate (or cerium oxide, sodium peroxide, ammonium persulphate, Potassium Persulphate).
Scheme 7: butyl (tetra) titanate 5%, stearic acid 3%, sodium stearate 3%, 1,2-propylene glycol 10%, ethanol 10%, all the other are Sodium Persulfate (or cerium oxide, sodium peroxide, ammonium persulphate, Potassium Persulphate).
Two, water-soluble inorganic oxygenant or water-soluble inorganic salt (as Sodium Persulfate) are before modified and modified scanning electron microscope (SEM) photograph, as shown in Figure 1, 2.
As can be seen from Fig. 1: the Sodium Persulfate surface of non-modified is in smooth form.
As can be seen from Fig. 2: through the material of modified Sodium Persulfate surface coverage one deck oleophilic drainage, and between Sodium Persulfate particle, occur the phenomenon of adhesion.
Three, apply:
By each 1.0g of Sodium Persulfate after before modified, be placed on respectively in the graduated cylinder of band grinding port plug and scale, then add white oil to 30 ml, shake 2 minutes, observe its sedimentation time, make following table.
As can be seen from following table, added after in white oil by unmodified Sodium Persulfate, Sodium Persulfate sinks to the end very soon, and all sedimentations; And add after in white oil through modified Sodium Persulfate, 49 ~ 57 seconds can be suspended in white oil, then slowly sink to the end.
As can be seen from Fig. 3: polyacrylonitrile is difficult to the Sodium Persulfate surface depositing or be wrapped in non-modified, makes its encapsulation rate lower.
As can be seen from Fig. 4: polyacrylonitrile can deposit or be wrapped in the Sodium Persulfate surface through modification completely, improves its encapsulation rate significantly.

Claims (1)

1. reduce the method for water-soluble inorganic salt at oil-soluble material median surface tension force, it is characterized in that first stearic acid and sodium stearate being dissolved in 1,2-PD, form mixing solutions; Then butyl (tetra) titanate and ethanol are added mixing solutions, react to after terminating under the envrionment temperature of 105 DEG C, temperature of reaction system is down to 90 DEG C, add water-soluble inorganic oxygenant or water-soluble inorganic salt again, react under agitation condition to terminating, through cooling, water-soluble inorganic oxygenant or the water-soluble inorganic salt of interfacial tension must be reduced; Described water-soluble inorganic oxygenant or water-soluble inorganic salt and butyl (tetra) titanate, stearic acid, sodium stearate, 1,2-propylene glycol, ethanol account for 69% ~ 92%, 1% ~ 5%, 0.5% ~ 3%, 0.5% ~ 3%, 5% ~ 10% and 1% ~ 10% of the total mass that feeds intake respectively; Described water-soluble inorganic oxygenant or water-soluble inorganic salt are Sodium Persulfate, or cerium oxide, or sodium peroxide, or ammonium persulphate, or Potassium Persulphate.
CN201310646408.1A 2013-12-06 2013-12-06 A kind ofly reduce water-soluble inorganic oxygenant or the water-soluble inorganic salt method at oil-soluble material median surface tension force Expired - Fee Related CN103613961B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310646408.1A CN103613961B (en) 2013-12-06 2013-12-06 A kind ofly reduce water-soluble inorganic oxygenant or the water-soluble inorganic salt method at oil-soluble material median surface tension force

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310646408.1A CN103613961B (en) 2013-12-06 2013-12-06 A kind ofly reduce water-soluble inorganic oxygenant or the water-soluble inorganic salt method at oil-soluble material median surface tension force

Publications (2)

Publication Number Publication Date
CN103613961A CN103613961A (en) 2014-03-05
CN103613961B true CN103613961B (en) 2015-08-19

Family

ID=50164682

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310646408.1A Expired - Fee Related CN103613961B (en) 2013-12-06 2013-12-06 A kind ofly reduce water-soluble inorganic oxygenant or the water-soluble inorganic salt method at oil-soluble material median surface tension force

Country Status (1)

Country Link
CN (1) CN103613961B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113637350A (en) * 2021-09-23 2021-11-12 杭州海迪斯新材料有限公司 Preparation process of easily dispersible organic bentonite in high-polarity solvent system

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1918071A (en) * 2004-02-06 2007-02-21 伊梅里斯矿物有限公司 Ultrafine natural ground brucite
CN101020777A (en) * 2007-03-19 2007-08-22 浙江工业大学 Coiled polybutene pipe with high heat conductivity and its prepn
CN101486847A (en) * 2009-02-24 2009-07-22 华南理工大学 Solid phase preparation and use of organic modified calcium based montmorillonite
CN103146026A (en) * 2013-03-21 2013-06-12 枣庄市三兴高新材料有限公司 Clay powder for improving vulcanization processability of rubber and preparation method for same
CN103333532A (en) * 2013-07-11 2013-10-02 合肥旭阳铝颜料有限公司 Aqueous bronze powder preparation method

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1918071A (en) * 2004-02-06 2007-02-21 伊梅里斯矿物有限公司 Ultrafine natural ground brucite
CN101020777A (en) * 2007-03-19 2007-08-22 浙江工业大学 Coiled polybutene pipe with high heat conductivity and its prepn
CN101486847A (en) * 2009-02-24 2009-07-22 华南理工大学 Solid phase preparation and use of organic modified calcium based montmorillonite
CN103146026A (en) * 2013-03-21 2013-06-12 枣庄市三兴高新材料有限公司 Clay powder for improving vulcanization processability of rubber and preparation method for same
CN103333532A (en) * 2013-07-11 2013-10-02 合肥旭阳铝颜料有限公司 Aqueous bronze powder preparation method

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
ATO纳米粉体的液相有机改性及其机理探讨;吴湘伟等;《湖南大学学报(自然科学版)》;20070325(第03期);第54页第1.2部分,表1,第55页2.2改性机理部分-第56页3结论部分 *

Also Published As

Publication number Publication date
CN103613961A (en) 2014-03-05

Similar Documents

Publication Publication Date Title
CN103599751B (en) The preparation method of thiol-functionalizedmagnetic magnetic silica nano-material
US11746023B2 (en) Basic copper chloride particulate matter and preparation method therefor
CN104250350A (en) Method for preparing porous polymer material with through-pore structure
CN102616795A (en) Method for preparing pure silicon-based mesoporous silica nanoparticles
CN102443173A (en) Low-viscosity methyl vinyl silicone oil and preparation method thereof
CN103613961B (en) A kind ofly reduce water-soluble inorganic oxygenant or the water-soluble inorganic salt method at oil-soluble material median surface tension force
CN106277014A (en) The method that dispersion surface modification prepares active superfine calcium carbonate in advance
CN105800619A (en) Internally hydrophilic and externally hydrophobic silicon oxide nanometer bottle and preparation method and application thereof
CN107522875B (en) Silver nanoparticle crosslinked hydrogel, and preparation method and application thereof
CN114618440A (en) Synthesis process of lithium salt adsorbent precursor
EP2823888B1 (en) Surface modification method of aluminum oxide carrier
CN106634058A (en) Particle surface treatment method for releasing settling rate of powder in terminal hydroxyl polymer
CN103864126B (en) Method for preparing suspended dispersing type calcium carbonate
CN108362669B (en) For detecting Al3+Organic fluorescent polydopamine nanoparticle solution and preparation method thereof
CN109142703B (en) Detection method of aflatoxin M1 based on water-soluble perovskite nanocrystal
CN106423039B (en) A kind of preparation method for repairing the particulate iron manganese composite oxide of heavy metal in water and phosphorus pollution
KR20130050447A (en) Amine functionalized mesoporous iron oxyhydroxide and method for fabricating the same
CN103771492B (en) Simple preparation method of flaky zinc oxide nano material
CN109201018A (en) A kind of preparation method and purposes of the mesoporous carbon film of La doped
CN110013833B (en) Preparation method of MgO/GQD/chitosan oligosaccharide/PVA composite adsorption film
CN103613078B (en) Method for carrying out oleophylic and hydrophobic modification on surface of water-soluble inorganic oxidant or inorganic salt
CN102557093B (en) Additive applied to process for producing aluminum oxide by bayer method and preparation method of additive
CN103754913B (en) A kind of simple method for preparing of aluminum hydroxide nanoparticle material
CN108793675B (en) The composition and method quenched for sludge
CN101218179B (en) Method for treatment of wastewater containing fumed silica

Legal Events

Date Code Title Description
PB01 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
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20150819

Termination date: 20181206

CF01 Termination of patent right due to non-payment of annual fee