序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
201 Nowe barwniki reaktywne, pochodne di(3-sulfopirydyno)triazyny oraz sposób ich wytwarzania PL39430311 2011-03-22 PL394303A1 2012-09-24 BLUS KAZIMIERZ; PALUSZKIEWICZ JOANNA
202 LIPOHYDROPHILIC GLYCEROL BASED POLYMERS AS DIGESTION AIDS FOR IMPROVING WOOD PULPING PROCESSES CA2792626 2011-03-09 CA2792626A1 2011-09-15 DUGGIRALA PRASAD; LI XIAOJIN HARRY
The invention provides a method of improving the digestion of wood chips into pulp. The method involves: adding a liphohydrophilic glycerol-based polymer additive to a solution used in the digestion process. This additive is unexpectedly effective at facilitating digestion. The branched and ether structure of the additive allows it to withstand the harsh nature of a highly alkaline environment. In addition, it is more soluble in high pH than other surfactants. The structure, resistance, and particular balance between hydrophobic and hydrophilic regions, causes the additive to increases the interaction between the wood chips and the digestion chemicals. This in turn reduces the costs, the amount of additive needed, and the amount of reject wood chunks that result from the digestion process.
203 Anthraquinone azo dyes DE60303206 2003-05-27 DE60303206T2 2006-07-20 TZIKAS ATHANASSIOS; CLEMENT ANTOINE; LAUK URS
204 ANTHRAQUINONE-AZO DYES AU2003238410 2003-05-27 AU2003238410A1 2003-12-19 TZIKAS ATHANASSIOS; CLEMENT ANTOINE; LAUK URS
205 Quater:rylene-tetra:carbo-bis:imide(s), including NIR fluorescent dyes DE19512773 1995-04-05 DE19512773A1 1996-10-10 LANGHALS HEINZ PROF DR; SCHOENMANN GEB HAUTMANN
Quaterylene-tetra-carbo-bisimides of formula (I) are new; R1 and/or R2 = H and/or isocyclic aryl, which pref. are mono- to tetra-, esp. mono- or bi-cyclic, e.g. (di)phenyl or naphthyl, or hetaryl, pref. mono- to tricyclic, opt. with condensed benzene ring(s), e.g. pyridyl, pyrimidyl, pyrazinyl, triazinyl, ((di)benzo)furanyl, pyrrolyl, ((di)benzo)thiophenyl, (iso)quinolyl, coumarinyl, (benz)imidazolyl, (benz)oxazolyl, indolyl, carbazolyl, pyrazolyl, imidazolyl, (benz)isoxazolyl, (benzo)thiazolyl, indazolyl, pyridazinyl, cinnolyl, quinazolyl, quinoxalyl, phthalazinyl, phthalazindionyl, phthalimidyl, chromonyl, naphtholactamyl, (benzo)pyridonyl, o-sulphobenzimidyl, malein-imidyl, naphtharidinyl, benzimidazolonyl, benzoxazolonyl, benzothiazolonyl, benzothiazolinyl, quinozolonyl, pyrimidyl, quinoxalonyl, phthalazonyl, di-oxa-pyrimidinyl, pyridonyl, iso-quinolonyl, (benz)isothioazolyl, indazolonyl, acridinyl, acridonyl, quinozolindionyl, benzoxazindionyl, benzoxazinonyl and phthalimidyl. The aryl, hetaryl gps. may have the usual substits. not imparting solubility in water, e.g. (a) halogen (Cl, Br, I or F) or (b) 1-18, pref. 1-12, esp. 1-8, more esp. 1-4 C alkyl, opt. substd. by e.g. F, OH, CN, -OCOR3, -OR4, -OCOOR3, -CON(R4)(R5) or -OCONHR3 (R3 = alkyl, aryl, e.g. naphthyl or benzyl, opt. substd. by halogen, alkyl or -O-alkyl, or heterocyclyl; R4, R5 = H, alkyl, opt. substd. by CN or OH, 3-24, pref. 5, 6, 12, 15, 16, 20 or 24 C cycloalkyl or (het)aryl, esp. phenyl, opt. substd. by halogen, alkyl or -O-alkyl; or R4 and R5 and one of the other R2 to R4 gps. = a 5-6-membered (hetero)ring, e.g. a pyridine, pyrrole, furan or pyran ring); (c) -OR6 (R6 = as R4); (d) CN; (e) -N(R4)(R5); (f) -COR3; (g) -N(R7)COR3 (R7 = H, alkyl, hydroxymethyl, 2-hydroxyethyl, cyanomethyl, methoxycarbonylmethyl, acetoxymethyl, benzyl, opt. substd. phenyl, cycloalkyl, thienyl, pyranylmethyl or furfuryl; (h) -N(R6)COOR3; (i) -N(R6)CON(R4)(R5); (j) -NHSO2R3; (k) -SO2R3 or -SOR3; (l) -SO2OR3; (m) -CON(R4)(R5); (n) -SO2N(R4)(R5); (o) -N=N-R8 (R8 = phenyl, opt. substd. by halogen, alkyl or -O-alkyl); (p) -OCOR3; or (q) -OCONHR3. Numerous suitable substits. for these gps. are claimed.
206 Color mixtures comprising same-colored azo dyes with a coupling component of the diaminopyridine DE4329915 1993-09-04 DE4329915A1 1995-03-09 LAMM GUNTHER DR; LOEFFLER HERMANN; REICHELT HELMUT DR
207 DD32257288 1988-12-05 DD300442A5 1992-06-11 KLEINE FRITZ; DASSLER WALTER; MATTHES INGEBORG
208 YELLOW DIAZOPIGMENTS ON BASE OF 4,4-DIAMINO-1,1-DIANTRAQUINOLINE CS337189 1989-06-05 CS337189A1 1990-12-13 FLORIAN CESTMIR ING
209 DE3249395C2 - DE3249395 1982-06-08 DE3249395C2 1987-12-10 HASHIMOTO, MITSURU, NUMAZU, SHIZUOKA, JP
210 IT2062578 1978-02-24 IT1158655B 1987-02-25
211 ANTHRAQUINONE-AZO COMPOUNDS, PROCESS FOR THEIR PREPARATION AND THEIR USE AS PIGMENTS DE3068346 1980-07-14 DE3068346D1 1984-08-02 ROLF MEINHARD DR; NEEFF RUTGER DR; MULLER WALTER
212 PROCESS FOR THE PREPARATION OF ANTHRAQUINONE-AZO COMPOUNDS IN940CA1979 1979-09-10 IN153568B 1984-07-28 FUCHS HERMANN
213 FR2366337B1 - FR7729355 1977-09-29 FR2366337B1 1984-03-09
214 PIGMENT DYES DE3161693 1981-06-11 DE3161693D1 1984-01-26 DIMROTH PETER DR; LOTSCH WOLFGANG DR
215 LIQUID CRYSTAL WITH AN INCORPORATED PLEOCHROIC ANTHRAQUINONE DYESTUFF AND ITS USE DE3160908 1981-02-24 DE3160908D1 1983-10-27 MOLLER ALEXANDER DIPL CHEM; SCHEROWSKY GUNTHER DR
216 New bisazo compounds, methods for their production and recording materials their use in electrophotographic DE3221642 1982-06-08 DE3221642A1 1983-01-13 HASHIMOTO MITSURU
217 MONOAZPIGMENTE. CH203478 1978-02-24 CH633570A5 1982-12-15 ROUECHE ARMAND DR
218 AZO COMPOUNDS GB7934711 1979-10-05 GB2036776B 1982-12-08
219 ANTHRAQUINONE-AZO COMPOUNDS THEIR PREPARATION AND THEIR USE AS DYESTUFFS GB7931973 1979-09-14 GB2032941B 1982-12-01
220 AZO COMPOUNDS GB8210168 1979-10-05 GB2097012A 1982-10-27
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