NO131417B - - Google Patents

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Info

Publication number: NO131417B
Authority: NO; Norway
Prior art keywords: gel; layer; substances; substance; solution
Prior art date: 1970-05-01

Application number

NO1519/71A

Other languages

English (en)

Norwegian (no)

Other versions

NO131417C (ru

Inventor

E S Roberts

Original Assignee

Treadwell Corp

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.)

1970-05-01

Filing date

1971-04-23

Publication date

1975-02-17

1971-04-23 Application filed by Treadwell Corp filed Critical Treadwell Corp

1975-02-17 Publication of NO131417B publication Critical patent/NO131417B/no

1975-05-28 Publication of NO131417C publication Critical patent/NO131417C/no

Links

239000000126 substance Substances 0.000 claims description 80
238000000034 method Methods 0.000 claims description 29
229920002307 Dextran Polymers 0.000 claims description 26
230000008961 swelling Effects 0.000 claims description 23
238000000926 separation method Methods 0.000 claims description 22
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 14
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 13
239000007788 liquid Substances 0.000 claims description 12
229920002472 Starch Polymers 0.000 claims description 11
239000008107 starch Substances 0.000 claims description 11
235000019698 starch Nutrition 0.000 claims description 11
238000010828 elution Methods 0.000 claims description 7
239000004375 Dextrin Substances 0.000 claims description 6
229920001353 Dextrin Polymers 0.000 claims description 6
235000019425 dextrin Nutrition 0.000 claims description 6
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 5
230000001588 bifunctional effect Effects 0.000 claims description 5
229920001577 copolymer Polymers 0.000 claims description 5
150000004676 glycans Chemical class 0.000 claims description 5
229920000642 polymer Polymers 0.000 claims description 5
229920001282 polysaccharide Polymers 0.000 claims description 5
239000005017 polysaccharide Substances 0.000 claims description 5
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 4
150000001720 carbohydrates Chemical class 0.000 claims description 4
235000014633 carbohydrates Nutrition 0.000 claims description 4
239000000203 mixture Substances 0.000 claims description 4
238000006116 polymerization reaction Methods 0.000 claims description 4
239000000600 sorbitol Substances 0.000 claims description 4
-1 sucrose Chemical class 0.000 claims description 4
239000004372 Polyvinyl alcohol Substances 0.000 claims description 3
239000012928 buffer substance Substances 0.000 claims description 3
229920002451 polyvinyl alcohol Polymers 0.000 claims description 3
229930006000 Sucrose Natural products 0.000 claims description 2
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
239000001913 cellulose Substances 0.000 claims description 2
229920002678 cellulose Polymers 0.000 claims description 2
235000010980 cellulose Nutrition 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
239000005720 sucrose Substances 0.000 claims description 2
150000005846 sugar alcohols Chemical class 0.000 claims description 2
125000003700 epoxy group Chemical group 0.000 claims 1
230000001105 regulatory effect Effects 0.000 claims 1
239000000499 gel Substances 0.000 description 90
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 41
239000000243 solution Substances 0.000 description 39
229960002086 dextran Drugs 0.000 description 25
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 18
238000006243 chemical reaction Methods 0.000 description 13
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 12
NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 12
239000002245 particle Substances 0.000 description 11
239000011800 void material Substances 0.000 description 10
239000011780 sodium chloride Substances 0.000 description 9
239000008363 phosphate buffer Substances 0.000 description 8
150000003839 salts Chemical class 0.000 description 8
102000009027 Albumins Human genes 0.000 description 6
108010088751 Albumins Proteins 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
102000008100 Human Serum Albumin Human genes 0.000 description 6
108091006905 Human Serum Albumin Proteins 0.000 description 6
102000004877 Insulin Human genes 0.000 description 6
108090001061 Insulin Proteins 0.000 description 6
229940125396 insulin Drugs 0.000 description 6
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 5
229910052921 ammonium sulfate Inorganic materials 0.000 description 5
235000011130 ammonium sulphate Nutrition 0.000 description 5
239000011324 bead Substances 0.000 description 5
239000000872 buffer Substances 0.000 description 5
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 4
102000001554 Hemoglobins Human genes 0.000 description 4
108010054147 Hemoglobins Proteins 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
239000001166 ammonium sulphate Substances 0.000 description 4
JXTHNDFMNIQAHM-UHFFFAOYSA-N dichloroacetic acid Chemical compound OC(=O)C(Cl)Cl JXTHNDFMNIQAHM-UHFFFAOYSA-N 0.000 description 4
239000003480 eluent Substances 0.000 description 4
238000002474 experimental method Methods 0.000 description 4
239000008103 glucose Substances 0.000 description 4
102000004169 proteins and genes Human genes 0.000 description 4
108090000623 proteins and genes Proteins 0.000 description 4
239000002904 solvent Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
102000004190 Enzymes Human genes 0.000 description 3
108090000790 Enzymes Proteins 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
108010040201 Polymyxins Proteins 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
239000000084 colloidal system Substances 0.000 description 3
229960000633 dextran sulfate Drugs 0.000 description 3
229940088598 enzyme Drugs 0.000 description 3
238000005194 fractionation Methods 0.000 description 3
102000004196 processed proteins & peptides Human genes 0.000 description 3
108090000765 processed proteins & peptides Proteins 0.000 description 3
238000000746 purification Methods 0.000 description 3
LSTZTHCEEPHCNQ-UHFFFAOYSA-N 3-(2,5-dioxabicyclo[2.1.0]pentan-3-yloxy)-2,5-dioxabicyclo[2.1.0]pentane Chemical compound C1(C2C(O2)O1)OC1C2C(O2)O1 LSTZTHCEEPHCNQ-UHFFFAOYSA-N 0.000 description 2
BAMIYHILDBHASH-UHFFFAOYSA-N 4-(2,5-dioxabicyclo[2.1.0]pentan-3-yloxy)butan-1-ol Chemical compound C1(C2C(O2)O1)OCCCCO BAMIYHILDBHASH-UHFFFAOYSA-N 0.000 description 2
ZFIVKAOQEXOYFY-UHFFFAOYSA-N Diepoxybutane Chemical compound C1OC1C1OC1 ZFIVKAOQEXOYFY-UHFFFAOYSA-N 0.000 description 2
229920000896 Ethulose Polymers 0.000 description 2
239000001859 Ethyl hydroxyethyl cellulose Substances 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
150000001413 amino acids Chemical class 0.000 description 2
239000000356 contaminant Substances 0.000 description 2
229960005215 dichloroacetic acid Drugs 0.000 description 2
235000019326 ethyl hydroxyethyl cellulose Nutrition 0.000 description 2
125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 2
239000008187 granular material Substances 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
239000000463 material Substances 0.000 description 2
239000002773 nucleotide Substances 0.000 description 2
125000003729 nucleotide group Chemical group 0.000 description 2
238000012856 packing Methods 0.000 description 2
239000011148 porous material Substances 0.000 description 2
239000012460 protein solution Substances 0.000 description 2
239000007858 starting material Substances 0.000 description 2
DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 description 1
USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
239000005695 Ammonium acetate Substances 0.000 description 1
102000004506 Blood Proteins Human genes 0.000 description 1
108010017384 Blood Proteins Proteins 0.000 description 1
XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 1
HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
102000057297 Pepsin A Human genes 0.000 description 1
108090000284 Pepsin A Proteins 0.000 description 1
108010093965 Polymyxin B Proteins 0.000 description 1
241000700605 Viruses Species 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000008351 acetate buffer Substances 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
229930013930 alkaloid Natural products 0.000 description 1
229940043376 ammonium acetate Drugs 0.000 description 1
235000019257 ammonium acetate Nutrition 0.000 description 1
RJGDLRCDCYRQOQ-UHFFFAOYSA-N anthrone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3CC2=C1 RJGDLRCDCYRQOQ-UHFFFAOYSA-N 0.000 description 1
239000003242 anti bacterial agent Substances 0.000 description 1
229940088710 antibiotic agent Drugs 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
239000003125 aqueous solvent Substances 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
230000001580 bacterial effect Effects 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
239000012620 biological material Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical class OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
230000007850 degeneration Effects 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000000975 dye Substances 0.000 description 1
238000007720 emulsion polymerization reaction Methods 0.000 description 1
239000007863 gel particle Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
150000002314 glycerols Chemical class 0.000 description 1
230000005484 gravity Effects 0.000 description 1
229920000669 heparin Polymers 0.000 description 1
229960002897 heparin Drugs 0.000 description 1
229940088597 hormone Drugs 0.000 description 1
239000005556 hormone Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
239000002609 medium Substances 0.000 description 1
FEMOMIGRRWSMCU-UHFFFAOYSA-N ninhydrin Chemical compound C1=CC=C2C(=O)C(O)(O)C(=O)C2=C1 FEMOMIGRRWSMCU-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229920001277 pectin Polymers 0.000 description 1
239000001814 pectin Substances 0.000 description 1
235000010987 pectin Nutrition 0.000 description 1
230000035515 penetration Effects 0.000 description 1
229940111202 pepsin Drugs 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920000024 polymyxin B Polymers 0.000 description 1
229960005266 polymyxin b Drugs 0.000 description 1
229920001184 polypeptide Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000011084 recovery Methods 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000012064 sodium phosphate buffer Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000011782 vitamin Substances 0.000 description 1
229940088594 vitamin Drugs 0.000 description 1
229930003231 vitamin Natural products 0.000 description 1
235000013343 vitamin Nutrition 0.000 description 1
229920003169 water-soluble polymer Polymers 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B17/00—Sulfur; Compounds thereof
- C01B17/69—Sulfur trioxide; Sulfuric acid
- C01B17/74—Preparation
- C01B17/76—Preparation by contact processes
- C01B17/765—Multi-stage SO3-conversion

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Inorganic Chemistry (AREA)
Catalysts (AREA)
Treating Waste Gases (AREA)
Exhaust Gas Treatment By Means Of Catalyst (AREA)
Solid-Sorbent Or Filter-Aiding Compositions (AREA)

NO1519/71A 1970-05-01 1971-04-23 NO131417C (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US3361470A	1970-05-01	1970-05-01

Publications (2)

Publication Number	Publication Date
NO131417B true NO131417B (ru)	1975-02-17
NO131417C NO131417C (ru)	1975-05-28

Family

ID=21871422

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
NO131417D NO131417L (ru)	1970-05-01
NO1519/71A NO131417C (ru)	1970-05-01	1971-04-23

Family Applications Before (1)

Application Number	Title	Priority Date	Filing Date
NO131417D NO131417L (ru)	1970-05-01

Country Status (13)

Country	Link
US (1)	US3671194A (ru)
JP (1)	JPS5221480B1 (ru)
AU (1)	AU2827771A (ru)
BE (1)	BE766159A (ru)
CA (1)	CA951083A (ru)
DE (1)	DE2121034A1 (ru)
ES (1)	ES390642A1 (ru)
FR (1)	FR2090591A5 (ru)
GB (1)	GB1314968A (ru)
NL (1)	NL7105830A (ru)
NO (2)	NO131417C (ru)
ZA (1)	ZA712185B (ru)
ZM (1)	ZM5171A1 (ru)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1981003654A1 (en) *	1980-06-19	1981-12-24	Boliden Ab	A method of manufacturing sulphuric acid
WO1983001438A1 (en) *	1981-10-26	1983-04-28	Boliden Ab	A method in the manufacture of sulphuric acid from gases generated in discontinuous processes

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2223131C3 (de) *	1972-05-12	1979-10-11	Davy Powergas Gmbh, 5000 Koeln	Verfahren zur Herstellung von Schwefelsäure aus Schwefel und Sauerstoff
DE2307973A1 (de) *	1973-02-17	1974-08-29	Metallgesellschaft Ag	Verfahren zur katalytischen umsetzung von so tief 2 zu so tief 3
JPS53128986U (ru) *	1977-03-19	1978-10-13
GB8524083D0 (en) *	1985-09-30	1985-11-06	Boc Group Plc	Oxidation method
US5851265A (en) *	1996-09-03	1998-12-22	Monsanto Company	Selective removal and recovery of sulfur dioxide from effluent gases using organic phosphorous solvents
CN1384805A (zh) *	1999-11-01	2002-12-11	孟山都公司	由二氧化硫制备三氧化硫、硫酸和发烟硫酸的方法
EP1114669B1 (en) *	2000-01-07	2006-08-23	Haldor Topsoe A/S	Process and apparatus for the removal of dust in a reaction zone
DE102009025510A1 (de) *	2008-12-20	2010-06-24	Bayer Technology Services Gmbh	Verfahren zur Herstellung von Schwefeltrioxid
WO2011147431A1 (en)	2010-05-27	2011-12-01	Haldor Topsoe A/S	Process and apparatus for sulphuric acid production
CN103459309A (zh)	2011-01-11	2013-12-18	阿尔比马尔公司	制备二氧化硫和三氧化硫的方法
WO2017068403A1 (en) *	2015-10-20	2017-04-27	Ashar Navin G	A process for the manufacture of sulfur dioxide, sulfur trioxide, sulfuric acid, and sulfonated compounds
CN106915731B (zh) *	2017-04-14	2023-08-08	双盾环境科技有限公司	一种可调式应用惰性触媒处理高浓度so2烟气生产so3气体的装置
CN109095441B (zh) *	2017-06-20	2022-01-07	中国瑞林工程技术股份有限公司	制备硫酸的方法

0
- NO NO131417D patent/NO131417L/no unknown
1970
- 1970-05-01 US US33614A patent/US3671194A/en not_active Expired - Lifetime
1971
- 1971-04-05 ZA ZA712185A patent/ZA712185B/xx unknown
- 1971-04-13 CA CA110,158,A patent/CA951083A/en not_active Expired
- 1971-04-19 ZM ZM51/71A patent/ZM5171A1/xx unknown
- 1971-04-19 GB GB2652571*A patent/GB1314968A/en not_active Expired
- 1971-04-22 FR FR7114441A patent/FR2090591A5/fr not_active Expired
- 1971-04-22 BE BE766159A patent/BE766159A/xx unknown
- 1971-04-23 NO NO1519/71A patent/NO131417C/no unknown
- 1971-04-27 ES ES390642A patent/ES390642A1/es not_active Expired
- 1971-04-28 NL NL7105830A patent/NL7105830A/xx unknown
- 1971-04-29 DE DE19712121034 patent/DE2121034A1/de active Pending
- 1971-04-29 AU AU28277/71A patent/AU2827771A/en not_active Expired
- 1971-05-01 JP JP46029407A patent/JPS5221480B1/ja active Pending

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1981003654A1 (en) *	1980-06-19	1981-12-24	Boliden Ab	A method of manufacturing sulphuric acid
WO1983001438A1 (en) *	1981-10-26	1983-04-28	Boliden Ab	A method in the manufacture of sulphuric acid from gases generated in discontinuous processes

Also Published As

Publication number	Publication date
NO131417L (ru)
DE2121034A1 (de)	1971-11-11
NO131417C (ru)	1975-05-28
ZA712185B (en)	1971-12-29
ZM5171A1 (en)	1972-02-21
ES390642A1 (es)	1974-04-01
NL7105830A (ru)	1971-11-03
GB1314968A (en)	1973-04-26
FR2090591A5 (ru)	1972-01-14
US3671194A (en)	1972-06-20
JPS5221480B1 (ru)	1977-06-10
CA951083A (en)	1974-07-16
AU2827771A (en)	1972-11-02
BE766159A (fr)	1971-10-22

Publication	Publication Date	Title
US3002823A (en)	1961-10-03	Process of separating materials having different molecular weights and dimensions
NO131417B (ru)	1975-02-17
US3959251A (en)	1976-05-25	Stabilized agar product and method for its stabilization
Porath et al.	1975	Agar derivatives for chromatography, electrophoresis and gel-bound enzymes: III. Rigid agarose gels cross-linked with divinyl sulphone (DVS)
NO116690B (ru)	1969-05-05
US4822535A (en)	1989-04-18	Method for producing small, spherical polymer particles
Lloyd	1970	The preparation of two insoluble forms of the phytohemagglutinin, concanavalin A, and their interactions with polysaccharides and glycoproteins
US5089272A (en)	1992-02-18	Process for producing capsules having a permeability-controllable membrane
EP0066165B1 (en)	1986-04-09	A totally porous activated gel
CN101218023B (zh)	2012-02-08	制备分离基质的方法
JP2746291B2 (ja)	1998-05-06	血液潅流用の改良された親和性担体
JPS627441A (ja)	1987-01-14	徐放性カプセルおよびその製法
JP5122958B2 (ja)	2013-01-16	クロマトグラフィーマトリックスの製造方法
JP2002263486A (ja)	2002-09-17	エンドトキシン吸着体、及びそれを用いたエンドトキシンの除去方法
JPS646201B2 (ru)	1989-02-02
EP0113749A1 (en)	1984-07-25	PROCESS FOR THE PREPARATION OF A CRYSTALLIZED CARBON HYDRATE MATRIX FOR BIOLOGICALLY ACTIVE SUBSTANCES.
CN107561179A (zh)	2018-01-09	一种交联透明质酸或其盐的交联度的测定方法
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