CN105254945A - Medical antibiotic bottle plug and preparation method thereof - Google Patents

Medical antibiotic bottle plug and preparation method thereof Download PDF

Info

Publication number
CN105254945A
CN105254945A CN201510678023.2A CN201510678023A CN105254945A CN 105254945 A CN105254945 A CN 105254945A CN 201510678023 A CN201510678023 A CN 201510678023A CN 105254945 A CN105254945 A CN 105254945A
Authority
CN
China
Prior art keywords
parts
medical content
mixture
preparation
thiuram
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
CN201510678023.2A
Other languages
Chinese (zh)
Inventor
金仲恩
全春兰
张帆
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.)
Suzhou Cosmetic New Materials Co Ltd
Original Assignee
Suzhou Cosmetic New Materials 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 Suzhou Cosmetic New Materials Co Ltd filed Critical Suzhou Cosmetic New Materials Co Ltd
Priority to CN201510678023.2A priority Critical patent/CN105254945A/en
Publication of CN105254945A publication Critical patent/CN105254945A/en
Pending legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The invention relates to a medical antibiotic bottle plug and a preparation method thereof. The medical antibiotic bottle plug comprises components in parts by mass as follows: 30-50 parts of isoprene rubber, 10-25 parts of oxidized butyl rubber, 0.8-1.8 parts of calcined argil, 0.6-1.5 parts of dithiocarbamate, 0.08-0.22 parts of p-phenylenediamine, 20-34 parts of lithopone, 2-6 parts of white oil, 0.02-0.06 parts of iron oxide red, 0.5-1.2 parts of N-cyclohexyl-2-benzothiazole sulfonamide, 0.5-1.2 parts of thiuram, 0.5-1.4 parts of sulfur, 2-7 parts of diphenyl silanediol and 23-35 parts of water. The bottle plug has good bacteria resistance and bacteriostasis functions and also has excellent elongation at break and tearing strength, high aging resistance coefficient and low fragmentation rate during three-needle puncture.

Description

A kind of medical Content Within Pharmaceutical Closure and preparation method thereof
Technical field
The present invention relates to technical field of composite materials, particularly relate to a kind of medical Content Within Pharmaceutical Closure and preparation method thereof.
Background technology
Medical grade rubber bottle stopper is the heat-resistant powder filler goods with definite shape, size, for the sealing of the medicinal ampuliform vessel port such as glass plastic.The usage quantity of medical grade rubber bottle stopper is very large, as also higher to its specification of quality time medical.Bottle stopper sizing material requires harmful solvends such as not leaded, mercury, arsenic, barium, with can powder charge agent inoperative, bottle stopper itself can not have ejecta.The sizing materials such as general NR, IIR and SBR make, and produce, be widely used in pharmacy and medical industry by compression molding.
The antibacterial effect of existing medical grade rubber bottle stopper is good not in the market, is easily infected with germs.Existing medical grade rubber bottle stopper aging coefficient is low simultaneously, tear strength is poor, Punching Fallen Scraps Ratio is not low in three needle penetrations, can not meet the high standard in doctor's use procedure.
Summary of the invention
the technical problem solved:good not for existing medical grade rubber bottle stopper antibacterial effect, aging coefficient is low, tear strength is poor, the three needle penetrations shortcoming such as Punching Fallen Scraps Ratio is not low, the invention provides a kind of medical Content Within Pharmaceutical Closure and preparation method thereof.
technical scheme:a kind of medical Content Within Pharmaceutical Closure, in mass parts containing following composition: polyisoprene rubber 30 ~ 50 parts, oxidation isoprene-isobutylene rubber 10 ~ 25 parts, calcinated argil 0.8 ~ 1.8 part, dithiocar-bamate 0.6 ~ 1.5 part, Ursol D 0.08 ~ 0.22 part, 20 ~ 34 parts, zinc sulfide white, white oil 2 ~ 6 parts, red iron oxide 0.02 ~ 0.06 part, N cyclohexyl 2 benzothiazole sulfenamide 0.5 ~ 1.2 part, thiuram 0.5 ~ 1.2 part, Sulfur 0.5 ~ 1.4 part, Diphenylsilanediol 2 ~ 7 parts, 23 ~ 35 parts, water.
The medical Content Within Pharmaceutical Closure of one described above, in mass parts containing following composition: polyisoprene rubber 35 ~ 45 parts, oxidation isoprene-isobutylene rubber 15 ~ 22 parts, calcinated argil 1 ~ 1.5 part, dithiocar-bamate 0.9 ~ 1.3 part, Ursol D 0.1 ~ 0.2 part, 23 ~ 30 parts, zinc sulfide white, white oil 3 ~ 5 parts, red iron oxide 0.03 ~ 0.05 part, N cyclohexyl 2 benzothiazole sulfenamide 0.8 ~ 1.1 part, thiuram 0.7 ~ 1 part, Sulfur 0.7 ~ 1.2 part, Diphenylsilanediol 3 ~ 6 parts, 26 ~ 32 parts, water.
The medical Content Within Pharmaceutical Closure of one described above, in mass parts containing following composition: polyisoprene rubber 38 parts, oxidation isoprene-isobutylene rubber 17 parts, calcinated argil 1.2 parts, dithiocar-bamate 1 part, Ursol D 0.13 part, 25 parts, zinc sulfide white, white oil 3.5 parts, red iron oxide 0.035 part, N cyclohexyl 2 benzothiazole sulfenamide 0.9 part, thiuram 0.8 part, Sulfur 0.9 part, Diphenylsilanediol 4 parts, 28 parts, water.
The medical Content Within Pharmaceutical Closure of one described above, in mass parts containing following composition: polyisoprene rubber 40 parts, oxidation isoprene-isobutylene rubber 19 parts, calcinated argil 1.3 parts, dithiocar-bamate 1.1 parts, Ursol D 0.15 part, 26 parts, zinc sulfide white, white oil 4 parts, red iron oxide 0.04 part, N cyclohexyl 2 benzothiazole sulfenamide 1 part, thiuram 0.85 part, Sulfur 1 part, Diphenylsilanediol 4.5 parts, 29 parts, water.
The preparation method of a kind of medical Content Within Pharmaceutical Closure described above, the step of this preparation method is as follows:
The first step: obtain mixture A by after polyisoprene rubber, oxidation isoprene-isobutylene rubber, calcinated argil, dithiocar-bamate, Ursol D, zinc sulfide white, white oil, red iron oxide, Sulfur mixing;
Second step: by mixture A rotating speed be 160 ~ 200r/min, temperature stirs 10 ~ 20min at being 100 ~ 120 DEG C, and then to mix with N cyclohexyl 2 benzothiazole sulfenamide, thiuram, Diphenylsilanediol, water, obtain mixture B;
3rd step: mixture B is joined blended in twin screw extruder, extrude, and carry out granulation, obtain particulate material, then the particulate material obtained is made medical Content Within Pharmaceutical Closure.
In second step described above by mixture A rotating speed be 160r/min, temperature stirs 10min at being 100 DEG C.
In second step described above by mixture A rotating speed be 180r/min, temperature stirs 15min at being 110 DEG C.
beneficial effect:medical Content Within Pharmaceutical Closure of one provided by the invention and preparation method thereof, this bottle stopper has good antibacterial and bacteriostasis, simultaneously this bottle stopper bottle closure of rubber tensile yield>=720%, tear strength>=27.3kNm -1, aging coefficient (70 DEG C × 72h)≤0.88, three needle penetration not Punching Fallen Scraps Ratio>=93%, antibacterial bacteriostatic rate reaches 99.9%.
Embodiment
embodiment 1
A kind of medical Content Within Pharmaceutical Closure, in mass parts containing following composition: polyisoprene rubber 30 parts, oxidation isoprene-isobutylene rubber 10 parts, calcinated argil 0.8 part, dithiocar-bamate 0.6 part, Ursol D 0.08 part, 20 parts, zinc sulfide white, white oil 2 parts, red iron oxide 0.02 part, N cyclohexyl 2 benzothiazole sulfenamide 0.5 part, thiuram 0.5 part, Sulfur 0.5 part, Diphenylsilanediol 2 parts, 23 parts, water.
A preparation method for medical Content Within Pharmaceutical Closure, the step of this preparation method is as follows:
The first step: obtain mixture A by after polyisoprene rubber, oxidation isoprene-isobutylene rubber, calcinated argil, dithiocar-bamate, Ursol D, zinc sulfide white, white oil, red iron oxide, Sulfur mixing;
Second step: by mixture A rotating speed be 160r/min, temperature stirs 10min at being 100 DEG C, and then mixes with N cyclohexyl 2 benzothiazole sulfenamide, thiuram, Diphenylsilanediol, water, obtains mixture B;
3rd step: mixture B is joined blended in twin screw extruder, extrude, and carry out granulation, obtain particulate material, then the particulate material obtained is made medical Content Within Pharmaceutical Closure.
The tensile yield of the medical Content Within Pharmaceutical Closure that the present embodiment provides is 720%, and tear strength is 27.3kNm -1, aging coefficient (70 DEG C × 72h) be 0.88, three needle penetrations not Punching Fallen Scraps Ratio be 93%, antibacterial bacteriostatic rate is 99.9%.
embodiment 2
A kind of medical Content Within Pharmaceutical Closure, in mass parts containing following composition: polyisoprene rubber 50 parts, oxidation isoprene-isobutylene rubber 25 parts, calcinated argil 1.8 parts, dithiocar-bamate 1.5 parts, Ursol D 0.22 part, 34 parts, zinc sulfide white, white oil 6 parts, red iron oxide 0.06 part, N cyclohexyl 2 benzothiazole sulfenamide 1.2 parts, thiuram 1.2 parts, Sulfur 1.4 parts, Diphenylsilanediol 7 parts, 35 parts, water.
A preparation method for medical Content Within Pharmaceutical Closure, the step of this preparation method is as follows:
The first step: obtain mixture A by after polyisoprene rubber, oxidation isoprene-isobutylene rubber, calcinated argil, dithiocar-bamate, Ursol D, zinc sulfide white, white oil, red iron oxide, Sulfur mixing;
Second step: by mixture A rotating speed be 200r/min, temperature stirs 20min at being 120 DEG C, and then mixes with N cyclohexyl 2 benzothiazole sulfenamide, thiuram, Diphenylsilanediol, water, obtains mixture B;
3rd step: mixture B is joined blended in twin screw extruder, extrude, and carry out granulation, obtain particulate material, then the particulate material obtained is made medical Content Within Pharmaceutical Closure.
The tensile yield of the medical Content Within Pharmaceutical Closure that the present embodiment provides is 724%, and tear strength is 27.8kNm -1, aging coefficient (70 DEG C × 72h) be 0.84, three needle penetrations not Punching Fallen Scraps Ratio be 94%, antibacterial bacteriostatic rate is 99.9%.
embodiment 3
A kind of medical Content Within Pharmaceutical Closure, in mass parts containing following composition: polyisoprene rubber 45 parts, oxidation isoprene-isobutylene rubber 22 parts, calcinated argil 1.5 parts, dithiocar-bamate 1.3 parts, Ursol D 0.2 part, 30 parts, zinc sulfide white, white oil 5 parts, red iron oxide 0.05 part, N cyclohexyl 2 benzothiazole sulfenamide 1.1 parts, thiuram 1 part, Sulfur 1.2 parts, Diphenylsilanediol 6 parts, 32 parts, water.
A preparation method for medical Content Within Pharmaceutical Closure, the step of this preparation method is as follows:
The first step: obtain mixture A by after polyisoprene rubber, oxidation isoprene-isobutylene rubber, calcinated argil, dithiocar-bamate, Ursol D, zinc sulfide white, white oil, red iron oxide, Sulfur mixing;
Second step: by mixture A rotating speed be 180r/min, temperature stirs 15min at being 110 DEG C, and then mixes with N cyclohexyl 2 benzothiazole sulfenamide, thiuram, Diphenylsilanediol, water, obtains mixture B;
3rd step: mixture B is joined blended in twin screw extruder, extrude, and carry out granulation, obtain particulate material, then the particulate material obtained is made medical Content Within Pharmaceutical Closure.
The tensile yield of the medical Content Within Pharmaceutical Closure that the present embodiment provides is 729%, and tear strength is 28.2kNm -1, aging coefficient (70 DEG C × 72h) be 0.83, three needle penetrations not Punching Fallen Scraps Ratio be 95%, antibacterial bacteriostatic rate is 99.9%.
embodiment 4
A kind of medical Content Within Pharmaceutical Closure, in mass parts containing following composition: polyisoprene rubber 38 parts, oxidation isoprene-isobutylene rubber 17 parts, calcinated argil 1.2 parts, dithiocar-bamate 1 part, Ursol D 0.13 part, 25 parts, zinc sulfide white, white oil 3.5 parts, red iron oxide 0.035 part, N cyclohexyl 2 benzothiazole sulfenamide 0.9 part, thiuram 0.8 part, Sulfur 0.9 part, Diphenylsilanediol 4 parts, 28 parts, water.
A preparation method for medical Content Within Pharmaceutical Closure, the step of this preparation method is as follows:
The first step: obtain mixture A by after polyisoprene rubber, oxidation isoprene-isobutylene rubber, calcinated argil, dithiocar-bamate, Ursol D, zinc sulfide white, white oil, red iron oxide, Sulfur mixing;
Second step: by mixture A rotating speed be 180r/min, temperature stirs 15min at being 110 DEG C, and then mixes with N cyclohexyl 2 benzothiazole sulfenamide, thiuram, Diphenylsilanediol, water, obtains mixture B;
3rd step: mixture B is joined blended in twin screw extruder, extrude, and carry out granulation, obtain particulate material, then the particulate material obtained is made medical Content Within Pharmaceutical Closure.
The tensile yield of the medical Content Within Pharmaceutical Closure that the present embodiment provides is 732%, and tear strength is 28.5kNm -1, aging coefficient (70 DEG C × 72h) be 0.81, three needle penetrations not Punching Fallen Scraps Ratio be 97%, antibacterial bacteriostatic rate is 99.9%.
embodiment 5
A kind of medical Content Within Pharmaceutical Closure, in mass parts containing following composition: polyisoprene rubber 40 parts, oxidation isoprene-isobutylene rubber 19 parts, calcinated argil 1.3 parts, dithiocar-bamate 1.1 parts, Ursol D 0.15 part, 26 parts, zinc sulfide white, white oil 4 parts, red iron oxide 0.04 part, N cyclohexyl 2 benzothiazole sulfenamide 1 part, thiuram 0.85 part, Sulfur 1 part, Diphenylsilanediol 4.5 parts, 29 parts, water.
A preparation method for medical Content Within Pharmaceutical Closure, the step of this preparation method is as follows:
The first step: obtain mixture A by after polyisoprene rubber, oxidation isoprene-isobutylene rubber, calcinated argil, dithiocar-bamate, Ursol D, zinc sulfide white, white oil, red iron oxide, Sulfur mixing;
Second step: by mixture A rotating speed be 180r/min, temperature stirs 15min at being 110 DEG C, and then mixes with N cyclohexyl 2 benzothiazole sulfenamide, thiuram, Diphenylsilanediol, water, obtains mixture B;
3rd step: mixture B is joined blended in twin screw extruder, extrude, and carry out granulation, obtain particulate material, then the particulate material obtained is made medical Content Within Pharmaceutical Closure.
The tensile yield of the medical Content Within Pharmaceutical Closure that the present embodiment provides is 735%, and tear strength is 28.8kNm -1, aging coefficient (70 DEG C × 72h) be 0.80, three needle penetrations not Punching Fallen Scraps Ratio be 98%, antibacterial bacteriostatic rate is 99.9%.
Above the embodiment of the present invention is described in detail, for one of ordinary skill in the art, according to the thought of the embodiment of the present invention, all will change in specific embodiments and applications, in sum, this description should not be construed as limitation of the present invention.

Claims (7)

1. a medical Content Within Pharmaceutical Closure, to it is characterized in that in mass parts containing following composition: polyisoprene rubber 30 ~ 50 parts, oxidation isoprene-isobutylene rubber 10 ~ 25 parts, calcinated argil 0.8 ~ 1.8 part, dithiocar-bamate 0.6 ~ 1.5 part, Ursol D 0.08 ~ 0.22 part, 20 ~ 34 parts, zinc sulfide white, white oil 2 ~ 6 parts, red iron oxide 0.02 ~ 0.06 part, N cyclohexyl 2 benzothiazole sulfenamide 0.5 ~ 1.2 part, thiuram 0.5 ~ 1.2 part, Sulfur 0.5 ~ 1.4 part, Diphenylsilanediol 2 ~ 7 parts, 23 ~ 35 parts, water.
2. the medical Content Within Pharmaceutical Closure of one according to claim 1, to it is characterized in that in mass parts containing following composition: polyisoprene rubber 35 ~ 45 parts, oxidation isoprene-isobutylene rubber 15 ~ 22 parts, calcinated argil 1 ~ 1.5 part, dithiocar-bamate 0.9 ~ 1.3 part, Ursol D 0.1 ~ 0.2 part, 23 ~ 30 parts, zinc sulfide white, white oil 3 ~ 5 parts, red iron oxide 0.03 ~ 0.05 part, N cyclohexyl 2 benzothiazole sulfenamide 0.8 ~ 1.1 part, thiuram 0.7 ~ 1 part, Sulfur 0.7 ~ 1.2 part, Diphenylsilanediol 3 ~ 6 parts, 26 ~ 32 parts, water.
3. the medical Content Within Pharmaceutical Closure of one according to claim 1, to is characterized in that in mass parts containing following composition: polyisoprene rubber 38 parts, oxidation isoprene-isobutylene rubber 17 parts, calcinated argil 1.2 parts, dithiocar-bamate 1 part, Ursol D 0.13 part, 25 parts, zinc sulfide white, white oil 3.5 parts, red iron oxide 0.035 part, N cyclohexyl 2 benzothiazole sulfenamide 0.9 part, thiuram 0.8 part, Sulfur 0.9 part, Diphenylsilanediol 4 parts, 28 parts, water.
4. the medical Content Within Pharmaceutical Closure of one according to claim 1, to is characterized in that in mass parts containing following composition: polyisoprene rubber 40 parts, oxidation isoprene-isobutylene rubber 19 parts, calcinated argil 1.3 parts, dithiocar-bamate 1.1 parts, Ursol D 0.15 part, 26 parts, zinc sulfide white, white oil 4 parts, red iron oxide 0.04 part, N cyclohexyl 2 benzothiazole sulfenamide 1 part, thiuram 0.85 part, Sulfur 1 part, Diphenylsilanediol 4.5 parts, 29 parts, water.
5. the preparation method of a kind of medical Content Within Pharmaceutical Closure according to claim 1, is characterized in that the step of this preparation method is as follows:
The first step: obtain mixture A by after polyisoprene rubber, oxidation isoprene-isobutylene rubber, calcinated argil, dithiocar-bamate, Ursol D, zinc sulfide white, white oil, red iron oxide, Sulfur mixing;
Second step: by mixture A rotating speed be 160 ~ 200r/min, temperature stirs 10 ~ 20min at being 100 ~ 120 DEG C, and then to mix with N cyclohexyl 2 benzothiazole sulfenamide, thiuram, Diphenylsilanediol, water, obtain mixture B;
3rd step: mixture B is joined blended in twin screw extruder, extrude, and carry out granulation, obtain particulate material, then the particulate material obtained is made medical Content Within Pharmaceutical Closure.
6. the preparation method of a kind of medical Content Within Pharmaceutical Closure according to claim 5, is characterized in that: in described second step by mixture A rotating speed be 160r/min, temperature stirs 10min at being 100 DEG C.
7. the preparation method of a kind of medical Content Within Pharmaceutical Closure according to claim 5, is characterized in that: in described second step by mixture A rotating speed be 180r/min, temperature stirs 15min at being 110 DEG C.
CN201510678023.2A 2015-10-20 2015-10-20 Medical antibiotic bottle plug and preparation method thereof Pending CN105254945A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510678023.2A CN105254945A (en) 2015-10-20 2015-10-20 Medical antibiotic bottle plug and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510678023.2A CN105254945A (en) 2015-10-20 2015-10-20 Medical antibiotic bottle plug and preparation method thereof

Publications (1)

Publication Number Publication Date
CN105254945A true CN105254945A (en) 2016-01-20

Family

ID=55094914

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510678023.2A Pending CN105254945A (en) 2015-10-20 2015-10-20 Medical antibiotic bottle plug and preparation method thereof

Country Status (1)

Country Link
CN (1) CN105254945A (en)

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56111659A (en) * 1980-02-08 1981-09-03 Hayakawa Rubber Co Ltd Prevention of corrosion
EP0510683A1 (en) * 1991-04-26 1992-10-28 Nissho Corporation Blood collecting tube
CN101104317A (en) * 2007-08-10 2008-01-16 湖北华强科技有限责任公司 Method for producing local diaphragm rubber bottle stopper
CN201139762Y (en) * 2007-09-19 2008-10-29 湖北华强科技有限责任公司 Medicinal partial film coating rubber plug
CN101376730A (en) * 2007-08-31 2009-03-04 谷其昌 Thermoplastic elastomer material, preparation thereof and method for manufacturing medicinal bottle stopper by using the same
CN101427979A (en) * 2007-11-09 2009-05-13 山东省药用玻璃股份有限公司 Method for preparing semi-coating medical rubber plug
CN203291228U (en) * 2013-06-20 2013-11-20 韩豫 Rubber plug with elastic membrane
CN103602027A (en) * 2013-11-18 2014-02-26 崇州君健塑胶有限公司 Transparent medical thermoplastic rubber plug and preparation method thereof

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56111659A (en) * 1980-02-08 1981-09-03 Hayakawa Rubber Co Ltd Prevention of corrosion
EP0510683A1 (en) * 1991-04-26 1992-10-28 Nissho Corporation Blood collecting tube
CN101104317A (en) * 2007-08-10 2008-01-16 湖北华强科技有限责任公司 Method for producing local diaphragm rubber bottle stopper
CN101376730A (en) * 2007-08-31 2009-03-04 谷其昌 Thermoplastic elastomer material, preparation thereof and method for manufacturing medicinal bottle stopper by using the same
CN201139762Y (en) * 2007-09-19 2008-10-29 湖北华强科技有限责任公司 Medicinal partial film coating rubber plug
CN101427979A (en) * 2007-11-09 2009-05-13 山东省药用玻璃股份有限公司 Method for preparing semi-coating medical rubber plug
CN203291228U (en) * 2013-06-20 2013-11-20 韩豫 Rubber plug with elastic membrane
CN103602027A (en) * 2013-11-18 2014-02-26 崇州君健塑胶有限公司 Transparent medical thermoplastic rubber plug and preparation method thereof

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
吕柏源 等: "《橡胶塑料加工成型和制品应用工程手册》", 30 April 2002, 化学工业出版社 *
橡胶工业手册编写小组: "《橡胶工业手册 第三分册》", 31 August 1976, 石油化学工业出版社 *
谢忠麟 杨敏芳 编: "《橡胶制品实用配方大全 第二版》", 29 February 2004, 化学工业出版社 *
颜丽 等: "医药包装用丁基橡胶瓶塞的材料选择", 《制品与工艺》 *
魏苏民 等: "氯化丁基橡胶抗生素瓶塞的研制", 《特种橡胶制品》 *

Similar Documents

Publication Publication Date Title
CN102936384B (en) Polyvinyl chloride (PVC) magnetic-plastic blending door gasket and manufacture method thereof
CN105885285A (en) Environmentally-friendly PVC (Polyvinyl Chloride) cable material
CN105254945A (en) Medical antibiotic bottle plug and preparation method thereof
CN103724915A (en) Environment-friendly flame-retardant automobile sealing strip
CN104725732B (en) Low-hardness medical thermoplastic brominated butyl rubber and preparation method thereof
CN111019255A (en) Antibacterial rubber material and preparation method thereof
CN103642137A (en) Rubber plug material for transfusion medicines and preparation method thereof
CN107903524A (en) A kind of plastic processing toughener and its preparation process
CN107619508A (en) A kind of rubber composite
CN102993493A (en) Medicinal synthetic polyisoprene gasket composition
CN106147240A (en) A kind of chilling shrink type cable accessory silicone rubber and preparation method thereof
CN109777001A (en) A kind of high tenacity medical PVC material and preparation method thereof
CN103724917A (en) Flame-retardant sealing strip for automobile
CN105949632A (en) Chemical-corrosion-resistant butyl rubber plug and preparation method thereof
CN102585310B (en) Medical sealing gasket and preparation method thereof
CN109370070A (en) A kind of freeze-drying additive chlorinated butyl rubber bung and preparation method thereof
CN103642135A (en) Rubber stopper material for cephalosporin drug and preparation method thereof
CN206033649U (en) Sealed plastic bottle lid
CN107722476B (en) Acid and alkali resistant medical rubber plug rubber material and rubber plug preparation process
CN104356446A (en) Medical grade rubber bottle plug and preparation method thereof
CN103214804B (en) Medicinal packing barrier film and preparation method thereof
CN106117653A (en) A kind of proof medical synthesized polyisoprene gasket
CN102993496A (en) Polyisoprene gasket composition for injection
CN106280500B (en) A kind of thermoplastic dynamic vulcanized brombutyl/polypropene composition and preparation method thereof
CN109867921A (en) A kind of PBS composite material and preparation method of the toughener containing PBST

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20160120

RJ01 Rejection of invention patent application after publication