CN1040331C - 静电复印碳粉分散剂的制造方法 - Google Patents
静电复印碳粉分散剂的制造方法 Download PDFInfo
- Publication number
- CN1040331C CN1040331C CN 92114791 CN92114791A CN1040331C CN 1040331 C CN1040331 C CN 1040331C CN 92114791 CN92114791 CN 92114791 CN 92114791 A CN92114791 A CN 92114791A CN 1040331 C CN1040331 C CN 1040331C
- Authority
- CN
- China
- Prior art keywords
- section
- carbon powder
- dispersing agent
- minutes
- degraded
- 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
Links
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 16
- 239000002270 dispersing agent Substances 0.000 title abstract 4
- 238000003672 processing method Methods 0.000 title abstract 2
- 238000002156 mixing Methods 0.000 claims abstract description 23
- 229920001903 high density polyethylene Polymers 0.000 claims abstract description 15
- 239000004700 high-density polyethylene Substances 0.000 claims abstract description 15
- 239000011347 resin Substances 0.000 claims abstract description 15
- 229920005989 resin Polymers 0.000 claims abstract description 15
- 239000005977 Ethylene Substances 0.000 claims abstract description 10
- 239000004743 Polypropylene Substances 0.000 claims abstract description 8
- 238000004519 manufacturing process Methods 0.000 claims abstract description 8
- 238000000034 method Methods 0.000 claims abstract description 8
- -1 polypropylene Polymers 0.000 claims abstract description 8
- 229920001155 polypropylene Polymers 0.000 claims abstract description 8
- 230000015556 catabolic process Effects 0.000 claims abstract description 7
- 229920001577 copolymer Polymers 0.000 claims abstract description 7
- 238000006731 degradation reaction Methods 0.000 claims abstract description 7
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 12
- 238000002844 melting Methods 0.000 claims description 11
- 230000008018 melting Effects 0.000 claims description 11
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 238000005507 spraying Methods 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 239000006185 dispersion Substances 0.000 claims description 8
- 239000000428 dust Substances 0.000 claims description 8
- 230000006378 damage Effects 0.000 claims description 3
- 238000012856 packing Methods 0.000 claims description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract description 5
- 239000002994 raw material Substances 0.000 abstract description 5
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 22
- 229910052757 nitrogen Inorganic materials 0.000 description 11
- 239000000463 material Substances 0.000 description 10
- 239000000843 powder Substances 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 5
- 239000007921 spray Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- VIKNJXKGJWUCNN-XGXHKTLJSA-N norethisterone Chemical compound O=C1CC[C@@H]2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 VIKNJXKGJWUCNN-XGXHKTLJSA-N 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 238000002329 infrared spectrum Methods 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 206010009866 Cold sweat Diseases 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- BLCKNMAZFRMCJJ-UHFFFAOYSA-N cyclohexyl cyclohexyloxycarbonyloxy carbonate Chemical compound C1CCCCC1OC(=O)OOC(=O)OC1CCCCC1 BLCKNMAZFRMCJJ-UHFFFAOYSA-N 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000005502 peroxidation Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- 229940070710 valerate Drugs 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Images
Landscapes
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
本发明提供一种静电复印碳粉分散剂及其制造方法。由聚丙烯、高密度聚乙烯及乙烯、丙烯共聚物的共混物,经热降解喷雾工艺制得的球形树脂。该碳粉分散剂能使复印碳粉分散性好,提高了涂复面的光泽度,清晰度,且与碳粉有良好的互溶性,抗湿性,原料来源广泛,廉价易得,制造工艺简单合理。
Description
本发明是关于静电复印技术中复印粉填加剂的制备方法。
静电复印粉的碳分散剂是复印粉的组分之一。其作用除了使复印粉很好地分散外,还提高了涂复表面的光泽度和清晰度。静电复印粉碳粉分散剂一般采用低分子量的烯烃聚合物,低分子量聚烯烃可以直接合成,也可以由聚烯烃的大分子降解得到。
US3,652,707;US3,652,706;CN87,101742A;US3,558,737:都是使用Friedel Crafts催化剂制备分子量在700-2500范围内的低分子聚合物。
US3,591,502;US3,997,624是使用过氧化苯甲酰,二环己基过氧化二碳酸酯,三丁基过氧化戊酸酯等催化剂进行游离基聚合制备低分子聚合物。
US3,892,717;JP59-206409;GB1,444,736是使用齐格勒型催化剂,如以沉积在锰化合物上的四氯化钛为催化剂,以三乙基铝为助催化剂,己烷为溶剂的乙烯聚合得到的分子量在2500左右的低分子聚合物。
日本专利特开平3-84009“低分子丙烯系聚合体及制造方法”给出一种由丙烯、乙烯及C4以上α烯烃的共聚物经热降解得到的数均分子量为1000到20000,软化点125-148℃,等规物含量70-84%,丙烯含量80-95%(摩尔比),乙烯含量5-20%(摩尔比)C4以上α烯烃含量0-15%(摩尔比)的低分子丙烯系聚合物。该种低分子聚合物如作为复印粉分散剂时还有较多的不足之处,因为是采用的共聚物为降解原料,共混物中乙烯含量一般在5-20%(摩尔比),当乙烯含量超出20%(摩尔比),共聚物发粘,加工困难。欲得到乙烯含量较高的低分子物,全部用共聚物为原料显然不能满足要求,加之共聚物原料成本高,来源不及均聚物广泛等诸多缺点,有待于进一步改进。
本发明提供一种静电复印碳粉分散剂及其制造方法,该种碳粉分散剂不但能使复印碳粉分散性好,提高了涂复面的光泽度、清晰度,且与碳粉有良好的互溶性,抗湿性,较高的软化点和粘度,原料来源广泛,兼价易得,制备工艺简单合理。
本发明采用聚丙烯,高密度聚乙烯及乙烯、丙烯共聚物的共混物经热降解,喷雾工艺后得到的球形树脂。该树脂数均分子量Mn在2000-10000之间,软化点在148-160℃、160℃的熔融粘度50-100毫帕·秒,树脂的红外光谱在波数为880厘米-1,1650厘米处有双键吸收峰,波数为720厘米-1处有乙烯吸收峰,色相小于2,挥发分小于1.0%,粒度<0.098毫米孔径的粒子占总粒子数的96%
本发明所用聚丙烯占共混树脂重量的50-90%,等规度90%以上,熔融指数0.5-15克/10分,高密度聚乙烯占共混树脂重量的10-50%,熔融指数0.3-3克/10分,乙烯丙烯共聚物占共混树脂重量的0-15%,共聚物中乙烯含量在3-20%(摩尔百分比),熔融指数0.5-15克/10分。
本发明碳粉分散剂的制造方法由下面几部分组成:
加料段→熔融段→降解段→混料段→喷雾段→包装,各段温度控制为加料段130-170℃,熔融段250-280℃,降解段340-400℃,混料段240-260℃,降解时间控制在0.4-3小时。制造工艺由单螺杆挤出机、管式降解器、装有搅拌器的混合罐及带有喷咀的喷雾装置组成。首先要将上述降解——喷雾系统用氮气吹扫排好,并将各段升到预定的温度,开启挤出机及混料罐搅拌机,将上述树脂的共混物由加料斗进入挤出机塑化,挤出机将塑化好的共混物推向熔融段,熔融好的物料连续进入降解段,降解后的低分子物料进入混料罐,在混料罐中进行充分混合后最后进入喷雾段,用高压气体为动力将低分子共混物由喷雾咀喷出进入成品料仓。所用的高压气体可以是干燥压缩空气或普通氮气。气体压力控制在0.1至0.4MPa,调整气体压力及喷雾咀孔径,达到调节产品粒度及粒度分布的目的。
说明书附图的图面说明:
附图1喷雾装置示意图
a为熔融低分子物料进口
b为高压气体入口
c为物料出口
附图2装置流程示意图
附图3产品红外谱图
实施例1:在由单螺杆65塑料挤出机,螺杆直径Φ65毫米,螺杆长径比为25,管式降解器直径Φ50毫米,管长5米,装有搅拌器的混料罐及带有喷咀的喷雾装置组成的降解喷雾装置中进行试验。
用氮气对整个系统进行置换,吹排20分钟后,在继续通氮条件下,将各段升温,加料段升至150℃,熔融段升至260℃,降解段升至370℃,混料罐为250℃。
启动挤出机及混料罐搅拌机,停通氮气,将熔融指数为1克/10分,等规度95%的聚丙烯55份,熔融指数为0.3克/10分的高密度聚乙烯40份,乙烯含量5%(摩尔比)的乙丙嵌共聚物5份组成的共混物,经预混合连续送入挤出机加料口,调整螺杆转速,控制降解时间为0.75小时,经混料罐搅拌均匀后,控制喷雾速度,用0.2MPa的干燥压缩空气将降解的低分子物料喷入成品罐,连续操作360小时,主动停机。共得球形树脂15吨,检查整个设备,未发现阻塞及积碳现象,产品性能如下:
Mn4400,160℃熔融粘度为70毫帕·秒,软化点149℃,色相<2,挥发份0.1%,产品粒度<0.098毫米孔径的粒子占总粒子数的96%。
将上述得到的球形树脂与静电复印用油墨加入双螺杆挤出机中,充分混合得到静电复印用墨粉,其中乙-丙低分子共混物占2.5%静电复印油墨97.5%,所得产品在复印机上应用,图象逼真,字迹清晰。实施例2 采用实施例1的降解设备,用氮气对整个系统置换20分钟,边通氮气边将各段升温至预定值:加料段为130℃,熔融段为280℃,降解段为395℃,启动挤出机与混料罐搅拌机,停通氮气,将熔融指数为3克/10分的等规度97%的聚丙烯75份,熔融指数为1克/10分的高密度聚乙烯20份,乙烯含量为10%(摩尔百分比)的乙丙共聚物5份组成的共混物连续送入挤出机料斗,调节螺杆转速,控制降解时间0.4小时,所得产品性能如下:
Mn4000,160℃的熔融粘度60毫帕·秒软化点为148℃,色相<2,挥发份0.1%。
用0.1Mpa干燥氮气将降解物料喷雾成型产品粒度<0.098毫米孔径的粒子占总粒子数的96%。
其它实施例见附表:
表1
* II% 表示聚丙烯的等规指数;** MI 表示树脂的熔融指数。
| 聚 丙 烯 | 高密度聚乙烯 | 乙丙共聚物 | 加料段℃ | 熔融段℃ | 降解段℃ | 降解时间[小时] | 喷 雾 | |||||||
| II*% | MI**克/10分 | 重量百分数% | MI克/10分 | 重量百分数% | 乙烯含量摩尔% | MI克/10分 | 重量百分数% | 气体种类 | 压力MPa | |||||
| 实施例1 | 95.0 | 1 | 55 | 0.3 | 40 | 5 | 2 | 5 | 150 | 260 | 390 | 0.75 | 空气 | 0.2 |
| 实施例2 | 97.0 | 3 | 75 | 1 | 20 | 10 | 7.4 | 5 | 130 | 280 | 395 | 0.4 | 氮气 | 0.2 |
| 实施例3 | 96.0 | 7 | 65 | 0.6 | 25 | 7 | 11.8 | 10 | 170 | 250 | 300 | 0.5 | 空气 | 0.25 |
| 实施例4 | 98.0 | 0.7 | 60 | 2 | 25 | 7 | 2.4 | 15 | 160 | 275 | 385 | 0.45 | 氮气 | 0.15 |
| 实施例5 | 97.5 | 4 | 70 | 3 | 20 | 10 | 4.3 | 10 | 140 | 270 | 375 | 0.6 | 空气 | 0.2 |
| 实施例6 | 98.5 | 0.5 | 80 | 0.4 | 15 | 20 | 1.5 | 5 | 165 | 265 | 350 | 2.0 | 空气 | 0.2 |
| 实施例7 | 97.5 | 4 | 65 | 0.6 | 35 | 0 | 0 | 0 | 155 | 255 | 370 | 1.5 | 空气 | 0.2 |
Claims (1)
1、一种静电复印碳粉分散剂的制造方法,其特征在于采用聚丙烯,高密度聚乙烯及乙烯丙烯共聚物的共混物经热降解、喷雾制得,所用聚丙烯占共混树脂重量的50-90%,等规度90%以上,熔融指数0.5-15克/10分,高密度聚乙烯占共混树脂重量的10-50%,熔融指数0.3-3克/10分,乙烯丙烯共聚物占共混树脂重量的0-15%,共聚物中乙烯含量在3-20%(摩尔百分比),熔融指数0.5-15克/10分,制造方法由下面几部分组成:加料段→熔融段→降解段→混料段→喷雾段→包装,各段温度控制为加料段130-170℃,熔融段250-280℃,降解段340-400℃,混料段240-260℃,降解时间控制在0.4-3小时,经降解后得到的低分子乙丙共混物经喷雾后制得产品。
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 92114791 CN1040331C (zh) | 1992-12-26 | 1992-12-26 | 静电复印碳粉分散剂的制造方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 92114791 CN1040331C (zh) | 1992-12-26 | 1992-12-26 | 静电复印碳粉分散剂的制造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1089277A CN1089277A (zh) | 1994-07-13 |
| CN1040331C true CN1040331C (zh) | 1998-10-21 |
Family
ID=4947113
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 92114791 Expired - Fee Related CN1040331C (zh) | 1992-12-26 | 1992-12-26 | 静电复印碳粉分散剂的制造方法 |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1040331C (zh) |
-
1992
- 1992-12-26 CN CN 92114791 patent/CN1040331C/zh not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CN1089277A (zh) | 1994-07-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1095854C (zh) | 具有极高透明度、增强的韧性、低排出性和易于加工的乙烯聚合物 | |
| DE69910612T2 (de) | Verfahren zur herstellung von pelletiertem polyolefin | |
| DE69320100T2 (de) | Teilchen mit einem Kern aus klebrigem Kunststoff und einer Schale aus teilchenförmigem Material | |
| CN101547943B (zh) | 减少聚烯烃中的凝胶的方法 | |
| EP0410914B1 (en) | Pourable particles of normally tacky plastic materials and process for their preparation | |
| DE69702627T2 (de) | Polymerisationsverfahren in einer Reaktorenreihe | |
| DE69632008T3 (de) | Extrudierter Film aus aethylencopolymeren Mischungen | |
| EP0728796A2 (en) | Process for improving processability of ultra low melt viscosity polymer | |
| KR940011143B1 (ko) | 압출성형 제품의 제조방법 및 장치 | |
| US8349423B2 (en) | Polyethylene composition for the production of peroxide crosslinked polyethylene | |
| CA2181617A1 (en) | Process for producing an in situ polyethylene blend | |
| DE69304032T2 (de) | Verfahren zur Herstellung von klebrigen Polymeren | |
| EP1237947B1 (en) | Process for reducing the weight average molecular weight and melt index ratio of polyethylenes and polyethylene products | |
| US3937772A (en) | Production of mixtures of plastics materials | |
| EP0757076A1 (en) | Process for the extrusion of polyethylene | |
| US5041259A (en) | Method for producing filler-containing colored thermoplastic resin composition | |
| CN1040331C (zh) | 静电复印碳粉分散剂的制造方法 | |
| US5041473A (en) | Process for producing carbon black filled polyethylene resins | |
| AU708276B2 (en) | High strength polyethylene film | |
| DE69811850T2 (de) | Extrusionsverfahren | |
| CA2163465A1 (en) | In situ polyethylene blend | |
| JP2025075447A (ja) | ペレットの製造方法、および、ペレットの製造装置 | |
| DE1957705A1 (de) | Verfahren zur Polymerisation von alpha-Olefinen | |
| KR20050105992A (ko) | 과산화물 가교된 폴리에틸렌을 생성하기 위한 폴리에틸렌조성물 |
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 | ||
| C15 | Extension of patent right duration from 15 to 20 years for appl. with date before 31.12.1992 and still valid on 11.12.2001 (patent law change 1993) | ||
| OR01 | Other related matters | ||
| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 19981021 Termination date: 20100126 |
