CN103030837B - Ultrafine methenamine production process - Google Patents

Ultrafine methenamine production process Download PDF

Info

Publication number
CN103030837B
CN103030837B CN201210073625.1A CN201210073625A CN103030837B CN 103030837 B CN103030837 B CN 103030837B CN 201210073625 A CN201210073625 A CN 201210073625A CN 103030837 B CN103030837 B CN 103030837B
Authority
CN
China
Prior art keywords
methenamine
urotropine
separator
products
production process
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.)
Active
Application number
CN201210073625.1A
Other languages
Chinese (zh)
Other versions
CN103030837A (en
Inventor
俞宏伟
方林木
崔涛
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.)
ZHEJIANG JINJU CHEMICAL CO Ltd
Original Assignee
ZHEJIANG JINJU CHEMICAL 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 ZHEJIANG JINJU CHEMICAL CO Ltd filed Critical ZHEJIANG JINJU CHEMICAL CO Ltd
Priority to CN201210073625.1A priority Critical patent/CN103030837B/en
Publication of CN103030837A publication Critical patent/CN103030837A/en
Application granted granted Critical
Publication of CN103030837B publication Critical patent/CN103030837B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention relates to an ultrafine methenamine production process. At present, products of the domestic methenamine production process are generally grain-shaped products, have particle sizes which are in commonly 150-200 mu m, and are directly provided to consumers, and the products are not further processed. The production process has the following steps: firstly, feeding methenamine raw materials into a material tank and then sending into a treater to carry out a surface modification treatment; secondly, introducing inert gas into a production device, and recycling by a fan; after the surface modification treatment is finished, sending the methenamine to a crusher through a feed tank to be crushed, wherein the particle size after crushing is controlled in the 5-70 mu m; finally, feeding the crushed methenamine enters into a separator and a dust collector to be separated, so as to obtain the finished products in the separator and the dust collector. The methenamine prepared by the method is applied to thermosetting phenolic resin, so that the mechanical strengths and the electric insulation properties of high-end products which are prepared by the thermosetting phenolic resin are improved.

Description

A kind of ultra-fine urotropine production technique
Technical field
The present invention relates to urotropine producing process, be specifically related to a kind of ultra-fine urotropine production technique.
Background technology
The important use of urotropine is the solidifying agent as resol.Resol not only can be for the manufacture of moulding compound, stratified plastics, porous plastics, cellularpiston etc., can also paint raw materials, glue paste, protection against corrosion be basic ion exchange resin with clay and the resol of take etc.Phenoplast and phenolic aldehyde insulation compound are widely used in machinery and electrical industry, its fast-developing history proves, exactly because its physical strength after solidifying of resol is high, stable performance, hard, wear-resisting, heat-resisting, resistance to combustion, resistance to most of chemical reagent, water absorbability is low, electrical insulation capability is excellent, dimensional stabilizing, cheap and become a kind of desirable material, and phenoplast are commonly called as " bakelite ".
Along with resol product is in the continuous increase of usage quantity of the product for civilian use, electric equipment products, automobile product and constantly widening of the field of use, the consumption of urotropine is also constantly improving.
Since 2003, along with the recovery of chemical industry, the market value of Chemicals is constantly being gone up, and China has the areas such as the north of resources advantage, large-scale methanol production enterprise constantly starts and goes into operation, as the product in methyl alcohol downstream, it is simple and easy to get that urotropine production has production technology, less investment, the feature of instant effect, market scale is constantly expanding, and it can be converted into solid phase prod by liquid product, regulates well the pressure in line balancing and alleviation market.
The product of current domestic urotropine production technique is generally grains product, and particle diameter generally, at 150-200 μ m, directly offers human consumer, product is not further processed.
As the urotropine of heat-reactive phenolic resin solidifying agent, there is following problem in common particle diameter urotropine:
(1). because urotropine particle is compared with large skewness, cause heat-reactive phenolic resin product physical strength to decline;
(2). because the larger reaction of urotropine particle is incomplete, at high temperature decomposite ammonia, cause heat-reactive phenolic resin product electrical insulation properties to decline.
Summary of the invention
The present invention is directed to the deficiencies in the prior art, a kind of ultra-fine urotropine production technique is provided.
The inventive method is specifically:
A. the incoming stock groove of urotropine raw material, then send into treater and carry out surface modification treatment, adding weight ratio is the agent of 0.05%-0.6% organic surface modification treatment.
B. production equipment passes into rare gas element, by blower fan, recycles, and control pressure is at 0.1-5KPa.
C. the urotropine after modification is sent into crusher for crushing by intake chute, and after pulverizing, granularity is controlled at 5-70 μ m.
D. the urotropine after pulverizing enters separator, fly-ash separator carries out separation;
E. finished product obtains respectively in separator and fly-ash separator.
The ash content of coal≤0.05% in the finished product obtaining in step e, water content≤0.35%.
Beneficial effect of the present invention is: the application of the urotropine that utilizes the inventive method manufacturing in heat-reactive phenolic resin, improves high-end product physical strength, electrical insulation properties that heat-reactive phenolic resin is manufactured.
Accompanying drawing explanation
Fig. 1 is apparatus structure schematic diagram used in the present invention.
In figure: 1, raw material tank; 2, treater; 3, intake chute; 4, pulverizer; 5, separator; 6, discharge port; 7, blower fan; 8, fly-ash separator; 9, displacement pipe; 10, rare gas element.
Embodiment
Below in conjunction with accompanying drawing, the invention will be further described.
As shown in Figure 1, the appliance arrangement that this technique uses comprises raw material tank 1, treater 2, intake chute 3, pulverizer 4, separator 5, blower fan 7, fly-ash separator 8 and displacement pipe 9.
Before whole device work, first utilize displacement pipe 9 that oxygen contained in system is removed, dust explosion prevention, then raw material urotropine enters treater 2 by raw material tank 1, adds organic surface modification treatment agent 0.05-0.6%(weight ratio); At production equipment, pass into rare gas element 10, the airflow circulation of whole system is used, and control pressure is at 0.1-5KPa; Urotropine enters intake chute 3 after surface modification treatment, then sends into pulverizer 4 and pulverize, and after pulverizing, granularity is controlled at 5-70 μ m; The gas that after pulverizing, product up to standard is driven by blower fan 7 is brought separator 5 into, the not separated thinner material getting off enters fly-ash separator 8 with the wind, last gas is connected with pulverizer import by pipeline, recycle, product, by discharge port 6 dischargings of separator 5 and fly-ash separator 8, weighs, stitches bag, packing after discharging.

Claims (2)

1. a ultra-fine urotropine production technique, is characterized in that the method comprises the following steps:
A. the incoming stock groove of urotropine raw material (1), then send into treater (2) and carry out surface modification treatment, adding weight ratio is the agent of 0.05%-0.6% organic surface modification treatment;
B. production equipment passes into rare gas element (10), by blower fan (7), recycles, and control pressure is at 0.1-5KPa;
C. the urotropine after modification is sent in pulverizer (4) and is pulverized by intake chute (3), and after pulverizing, granularity is controlled at 5-70 μ m;
D. the urotropine after pulverizing enters separator (5), fly-ash separator (8) carries out separation;
E. finished product obtains respectively in separator (5) and fly-ash separator (8).
2. a kind of ultra-fine urotropine production technique according to claim 1, is characterized in that: the ash content of coal≤0.05% in the finished product obtaining in step e, water content≤0.35%.
CN201210073625.1A 2012-03-20 2012-03-20 Ultrafine methenamine production process Active CN103030837B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201210073625.1A CN103030837B (en) 2012-03-20 2012-03-20 Ultrafine methenamine production process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201210073625.1A CN103030837B (en) 2012-03-20 2012-03-20 Ultrafine methenamine production process

Publications (2)

Publication Number Publication Date
CN103030837A CN103030837A (en) 2013-04-10
CN103030837B true CN103030837B (en) 2014-04-16

Family

ID=48018266

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201210073625.1A Active CN103030837B (en) 2012-03-20 2012-03-20 Ultrafine methenamine production process

Country Status (1)

Country Link
CN (1) CN103030837B (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN2885417Y (en) * 2006-03-29 2007-04-04 闽西丰力粉碎机械有限公司 Integral crusher for material fining and modified processing
CN101433876A (en) * 2008-12-02 2009-05-20 北京航空航天大学 Integrated device for airflow pulverization and surface modification and technique thereof for preparing ultrafine grain
CN201333422Y (en) * 2008-12-02 2009-10-28 北京航空航天大学 Air-flow crushing and surface modification integrated device for preparing ultra-fine grains
CN102351230A (en) * 2011-07-06 2012-02-15 湖南磊鑫新材料科技有限公司 Preparation method of ultrafine active heavy calcium carbonate

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN2885417Y (en) * 2006-03-29 2007-04-04 闽西丰力粉碎机械有限公司 Integral crusher for material fining and modified processing
CN101433876A (en) * 2008-12-02 2009-05-20 北京航空航天大学 Integrated device for airflow pulverization and surface modification and technique thereof for preparing ultrafine grain
CN201333422Y (en) * 2008-12-02 2009-10-28 北京航空航天大学 Air-flow crushing and surface modification integrated device for preparing ultra-fine grains
CN102351230A (en) * 2011-07-06 2012-02-15 湖南磊鑫新材料科技有限公司 Preparation method of ultrafine active heavy calcium carbonate

Also Published As

Publication number Publication date
CN103030837A (en) 2013-04-10

Similar Documents

Publication Publication Date Title
CN103011151B (en) Method for preparing graphene/nickel nanocomposite material by utilizing gamma ray
CN102583333A (en) Method for synthesizing porous nanographite flakes by using corn stalks as carbon source
CN104310376A (en) Postprocessing crosslinking method of hydrothermally carbonized spherical particles of biomass carbon source material
CN103199319B (en) Method for recycling lithium cobalt oxide from waste positive electrode of lithium cobalt oxide battery
CN102367319A (en) Wood-plastic door sheet
CN103433502A (en) High-dispersing silver powder and preparation method thereof
CN101747585A (en) Method for preparing thermosetting plastic with coal gangue modified phenolic resin
CN103030837B (en) Ultrafine methenamine production process
CN103964812B (en) Vitrified brick being main raw material with brown coal germanium tailings and preparation method thereof
CN201644395U (en) Composite outer classifier
CN103304843A (en) Process method for producing butyl reclaimed rubber
CN103466974A (en) High-performance cement as well as preparation method thereof
CN201713471U (en) Thermal insulation water-proof environment-friendly coating production device
CN203955698U (en) A kind of waste separation treatment system
CN203696781U (en) Sand material feeding mechanism
CN205472686U (en) Device with useless non - metal powder of circuit board preparation active carbon
CN102816620B (en) Lignite drying method
CN104262676B (en) A kind of method recycling polyacrylamide superfines
CN103663507A (en) Method for preparing pure natural magnesium hydroxide flame retardant
CN103059342A (en) Modified polyethylene double-wall l corrugated pipe drying agent and preparation method thereof
CN203210563U (en) Plastic crusher
CN205216928U (en) Circular cone machine of adjustable feed inlet size
CN202951441U (en) Device for adding hot water to mixing machine
CN202200426U (en) Pelleting machine for recovering extruded sheets
CN203428926U (en) Processing device of organic attapulgite

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