Novel purpose of 4-(4-methyl-3-pentenyl)-4-cyclohexene-1, 2-diacid anhydride

A technology based on pentenyl and cyclohexene, which is applied in the field of 4--4-cyclohexene-1, can solve the problems of complex additive structure, increased solder composition, complex composition, etc., and achieves easy cleaning, less residue, Synthetic easy effects

Inactive Publication Date: 2005-03-16
HARBIN UNIV OF COMMERCE
View PDF5 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although all have been improved, there are problems such as increasing the solder composition, complicating the composition, increasing the cost, or complicating the structure of the additive and making it difficult to synthesize.
On the other hand, the use of monoterpene derivative 4-(4-methyl-3-pentenyl)-4-cyclohexene-1,2-dioic anhydride is extremely limited. In addition to the role, no other uses have been found

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Novel purpose of 4-(4-methyl-3-pentenyl)-4-cyclohexene-1, 2-diacid anhydride
  • Novel purpose of 4-(4-methyl-3-pentenyl)-4-cyclohexene-1, 2-diacid anhydride

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0012] The specific preparation method is: taking the monoterpene compound β-myrcene and maleic anhydride as raw materials, under heating, after dripping β-myrcene to maleic anhydride, intermolecular Diels-Alpha Diels-Alder cycloaddition reaction. The product is obtained by collecting fractions at 155-160°C / 3mmHg by vacuum distillation. The crude reaction product and the vacuum distillation product after the reaction were respectively used as welding fluxes for welding activity test.

[0013] The raw material β-myrcene is an important fragrance and the basic raw material of synthetic fragrance. It can be easily prepared in large quantities from β-pinene, one of the main components of turpentine oil.

[0014] Welding activity test

[0015] The welding activity test follows the method stipulated by JIS-Z-3197 in Japan. The spread rate of solder when the new soldering flux is used on the copper plate is measured. Compared with the reference material rosin, the larger the spread rate,...

Embodiment 1

[0016] Example 1 (Preparation of 4-(4-methyl-3-pentenyl)-4-cyclohexene-1,2-dianhydride)

[0017] In a four-necked flask equipped with a thermometer, a dropping funnel, a mechanical stirrer, and a condenser, add maleic anhydride (1.0 times mole calculated as β-myrcene) and heat to dissolve the maleic anhydride, and control it to 65- At 70°C, β-myrcene (β-myrcene content 75%) was added dropwise from the dropping funnel. After dripping, react at 65-70°C for 4 hours. The crude product obtained by distilling off low-boiling components is used as solder A for soldering test. The product 4-(4-methyl-3-pentenyl)-4-cyclohexene-1,2-dianhydride was collected by vacuum distillation to collect the fraction at 155-160℃ / 3mmHg, and the structure was determined by nuclear magnetic resonance as Flux B is used for welding test.

Embodiment 2

[0018] Example 2 (Measurement of Welding Activity)

[0019] The soldering activity test follows the method specified by JIS-Z-3197 in Japan, using H60A type solder with a diameter of 1.6mm, and rosin as a comparative substance.

[0020] The 20mm*20mm*0.3mm copper plate was washed with isopropanol and heated and oxidized at 150°C for 1 hour. Weigh 0.250mg±0.01 solder and roll it into a circle shape and place it on the copper plate. Place the solder sample to be measured in the center of the circular solder. The sample weight is 25mg±5. Put the above copper plate on the heating plate and control the heating for 4 minutes. When the temperature reaches 200°C, cut off the power, and after cooling, use monoterpenes such as limonene and pinene as a solvent to wash the copper plate to remove. Measure the thickness and diameter of the expanded solder. Use the following formula to calculate the expansion rate of the solder. The larger the expansion rate value is Means the higher the activit...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
Diameteraaaaaaaaaa
Login to view more

Abstract

The invention relates to an annular monoterpene derivative used as new bonding glue. The annular monoterpene derivative 4-4- cyclohexene -1,2-biacidic can bond the electric unit on the copperplate, and has high active welding property, leaves little draff, needs only low temperature, and is easy to wash. The active component is annular monoterpene derivative that has acid anhydride, and is made from Beta-myrcene and maleic anhydride through Diels-Alder molecule cycloaddition reaction. It can be used for welding the electric units on circuit board with soldering tin and production of other electric unit needing bonding electric unit.

Description

Technical field: [0001] The invention relates to a new use of 4-(4-methyl-3-pentenyl)-4-cyclohexene-1,2-dianhydride. As a new type of soldering agent, it can be used in the production of electronic products that require soldering During the soldering process of electronic components. Background technique: [0002] In the production process of electronic products, in order to fix the electronic components on the circuit board, solder is indispensable. Rosin is a well-known and commonly used solder. The big disadvantage of rosin is that it is easy to leave a lot of residues after welding. These residues not only cause poor conductivity but also become inspection obstacles in the automated inspection process. The residues must be removed. For this reason, people have adopted halogens with strong washing performance. Solvents, however, halogen-based solvents have been restricted in their environmental damage. In addition, heating is indispensable in the soldering process. Applying hi...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): B23K35/36C07D307/89H05K3/34
Inventor 陆占国李健韩毓杰
Owner HARBIN UNIV OF COMMERCE
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap