国际知名品牌Target Mol与Topscience开展战略合作？ 2014 年 12 月， Topscience 与 TargetMol 正式签署为期三年的战略合作协议，作为 Target Mol 在大中国地区的服务机构，陶素将负责 TargetMol 在中国市场的产品销售、技术应用与支持等各项业务，为中国大陆及包括台湾，香港和澳门在内的大中国地区客户提供快速，便捷的服务 Topscience 将始终秉承“ Chemistry for a better life ” 之理念，一如既往地为中国化学行业广大科研和生产用户提供品质卓越的产品与一流的服务！ TargetMol 位于美国生物医药最发达的马赛诸塞州，这里有多达 900 家 Healthcare 领域的公司，从大型医院到生物技术公司，都对药物小分子的研究注以浓厚的兴趣。为了以最快的速度获得新型药物分子或进行细胞诱导的实验，研究者利用已经上市或报道的药物小分子进行老药新用或信号通路的研究。但通常这些药物小分子的收集工作是非常繁琐的，会耗费科学家们大量的时间。同时，由于分子和细胞水平的实验用量较小，又增加了对实验材料的浪费。为了解决这个问题， TargetMol 公司推出了各种上市药物小分子库和活性 抑制剂 小分子库，以 1mg ， 5mg 的干粉和 10mM 的溶液向医药领域的客户提供灵活的产品集合，帮助生物学家和药学家得到了具有明确活性和毒性的上市药物研究的小分子，并收集了大量的抑制剂小分子以供科学家们进行细胞信号转导，细胞诱导，老药新用以及阳性对照的实验。 在未来的三年中，TargetMol将授权Topscience经营其中国市场业务，依靠Topscience强大的市场优势和TargetMol自身产品的竞争力，为中国的生物，药学和化学家们提供更加便捷和优质的活性小分子化合物。 Target Mol 的优势产品系列摘录如下： 1. USA Drug Collection USA Drug Collection has already been put into the market, including1280 kinds of small molecular drug compounds in the America. These medicinesare assigned by USP or USAN. There are different format for these drugcompounds 1mg, 5mg and DMSO 10mM dissolvent concentration. All the compounds inthis library not only make bioassay experiments, but also finish clinicaleffective assessment. Every compound includes product data information indetail. Such as structure, CAS number, molecular formula, molecular weight,bioactivity and commodity name. Pharmacology and toxicology referencedocumentation is also included. Advantages There are rich document references and reliable data demonstrations.Every compound is selected by medicinal and biological chemist, has goodbiological activity and structural diversity. These medicines corresponding disease and medicine toxicologicaldocument has been open in public. You can be fully supported by toxicologicaldata and find new functions. The average purity is above 95%. If there are no specialinstructions, purity of every compound are all higher than 90%. Applications It is adopted by new users for old drugs, module establishment, drugselection experiments and so on. On the one hand, we offer convenient researchtools for known medicinal activity assessment. On the other hand, we offerexcellent research tools to cell biologist to conduct cell induce experiment. Package condition Dry chemical powder quality guarantee period is more than 1 year. We suggest liquor products are used up in 6 months. Because withrepeated frosted, it is possible to appear products’ degradation. The delivery cost is different depending on the customers’ countries. The list price for the USA Drug Collection is as follows. 250ul 10mM concentration in DMSO solution of USA Drug Collection:12800 USD 500ul 10mM concentration in DMSO solution of USA Drug Collection:18602 USD 1ml 10mM concentration inDMSO solution of USA Drug Collection: 23688 USD 1mg USA Drug Collection:12800USD 5mg 1280 USA Drug Collection: 37120 USD 2.Selective Drug Collection The selective Drug Collection including 400 kinds of small moleculardrug on the America, Europe and Asia market. These medicines are certified byUSP, USAN, INN, BAN, JAN and so on. All are in stock, twelve 96 plate, is DMSO10mM dissolvent concentration. Different from other products on the market, the400 products not only make bioassay experiments, but also finish clinicaleffective assessment. Every compound includes product data information indetail. Such as structure, CAS number, molecular formula, molecular weight,bioactivity and commodity name. Pharmacology and toxicology referencedocumentation is also included. Advangtages There are rich document references and reliable data demonstrations.Every compound is selected by medicinal and biological chemist, has goodbiological activity and structural diversity. These medicines corresponding disease and medicine toxicologicaldocument has been open in public. You can be fully supported by toxicologicaldata and find new functions. The average purity is above 95%. If there are no specialinstructions, purity of every compound are all higher than 90%. Application It is adopted by new users for old drugs, module establishment, drugselection experiments and so on. On the one hand, we offer convenient researchtools for known medicinal activity assessment. On the other hand, we offerexcellent research tools to cell biologist to conduct cell induce experiment. Package condition We can offer 1mg to 5mg packing dry powder, and also can provide10mmol/L DMSO solution. Dry chemical powder quality guarantee period is morethan 1 year. We suggest liquor products are used up in 6 months. Because withrepeated frosted, it is possible to appear products’ degradation. 250ul 10mM concentration in DMSO solution: 4,000 USD 500ul 10mM concentration in DMSO solution: 5,950 USD 1ml 10mM concentration inDMSO solution: 7,900 USD 1mg Drug Collection: 4,000USD 5mg Drug Collection:11,500USD 3 ． HTS Drug Collection HTS Drug Collection has already emerged into the market, including2000 kinds of small molecular drug on in the North AmericanAmerica, Europeanand Asian market. These medicines are certified by USP,USAN, INN, BAN, JAN andso on. All are in stock, twelve 96 plate, is withDMSO 10mMdissolventconcentration in DMSO. Different from other products on in themarket, the 2000 products have been certified not only make by bioassayexperiments, but also finish through clinical effective assessment. Everycompound includes product data information in detail. Such, such as structure,CAS number, molecular formula, molecular weight, bioactivity and commodityname. Pharmacology and toxicology reference documentation is also included. Advantages There are rich abundent abundant document references and reliabledata demonstrations. Selected by medicinal and biological chemist, eEverycompound is selected by medicinal and biological chemist, has good biologicalactivity and structural diversity. Disease targeted by tThese medicines corresponding disease andmedicine toxicological document has have been open in public. You can be fullysupported by toxicological data and find new functions. The average purity is above 95%. If there are no special instructionsnotice,purity of every compound are all higher than 90%. Applications It is adopted by in new users research/disease for old drugs, moduleestablishment, drug selection experiments and so on. On the one hand, we offerconvenient research tools for known medicinal activity assessment. On the otherhand, we offer excellent research tools to for cell biologist to conduct cellinduce experiment. There are two examples, one is MItifus, which is was used for curingmammary cancer and , now it treats leishmanisis (leishmaniasis is zoonosiscaused by leishmansia) It is transmitted by articulate and arthropods. Thisdisease is happened in more than 100 countries. Every year the number of newcases is more than 40 million, causing 5 million people death. Another theother one is Viagra. This disease is used for curing new colic, while clinicaleffect is less than expected, but in America in Pfizer Company’s at AusterBuilding accidently found that indViagra made some patients with heart diseasetake Viagra because of heart disease,causing Penis smooth musclerelaxationbecauserelaxation because of side effect. Because ofWith blowingblood increasing, it improves improved erectile function. Then through repeatedexperiment, it is was certified that Viagra iswas definitely effective for erectile function. Package condition We can offer not only 1mg to 5mg packing dry powder, and but alsocan provide 10mmol/L DMSO solution. The war renty for dDry chemical powderquality guarantee period is more than 1 year. We suggest that liquor productsare should be used up in within 6 months. Because withWith repeated frosted, itis possible to appear products’ degradation. The list price for the HTS Drug Collection is as follows. 250ul 10mM concentration in DMSO solution of USA DrugCollection: 199,700 USD 500ul 10mM concentration in DMSO solution of USA DrugCollection: 299,500 USD 1ml 10mM concentration inDMSO solution of USA Drug Collection: 399,300 USD 1mg USA Drug Collection: 199,700 USD 5mg 1280 USA Drug Collection: 599,950 USD 4. Europe&Asia Durg Collection Our drug compounds Collection including 480 kinds of small moleculardrug marketed in Europe and/or Asia. These medicines are certified by INN / BAN/ JAN and so on. Different from other products on the market, the 480 productsnot only make bioassay experiments, but also finish clinical effectiveassessment. Every compound includes product data information in detail. Such asstructure, CAS number, molecular formula, molecular weight, bioactivity andcommodity name. Pharmacology and toxicology reference documentation is alsoincluded. Advantages There are abundantdocument references and reliable datademonstrations. Every compound selected by medicinal and biological chemisthasgood biological activity and structuraldiversity. These medicines corresponding disease and medicine toxicologicaldocument has been open in public. You can be fully supported by toxicologicaldata and find new functions. The average purity is above 95%. If there are no special instructions,purity of every compound are all higher than 90%. Applications It is adopted by new users for old drugs, module establishment, drugselection experiments and so on. On the one hand, we offer convenient researchtools for known medicinal activity assessment. On the other hand, we offerexcellent research tools to for cell biologist to conduct cell induceexperiment. Package condition We can offer not only 1mg to 5mg packing dry powder, and butalso canprovide 10mmol/L DMSO solution. Dry chemical powder qualityThe guaranteewarrantyperiod for dry chemical powderis more than 1 year. We suggest liquorproducts are used up in 6 months. Because withWith repeated frosted, it ispossible to appear products’ degradation. The list price for the Europe &Asia Drug Collection is asfollows. 250ul 10mM concentration in DMSO solution: 4,800 USD 500ul 10mM concentration in DMSO solution: 7,200 USD 1ml 10mM concentration inDMSO solution: 9,500 USD 1mg USA Drug Collection:4,800 USD 5mg 1280 USA Drug Collection: 13,900 USD 5. Natural Compounds Library Natural compounds are famous for the novelty of the structures.There are 800 natural products in our Natural compoundslibrary.These naturalproduct screening compounds was refinedfrom plants and microorganisms. Mostcompounds have purity above 90% on average. The structures and stereochemistryare confirmed by various physicochemical analytical methods, including NMR,mass spectroscopy and in some cases X-ray analysis. They are supplied in96-well format, with other formats available upon request.We welcomecherry-picking of individual natural products from our Natural compoundslibrary. The list price for the Collection is as follows. 250ul 10mM concentration in DMSO solution: 11,500 USD 500ul 10mM concentration in DMSO solution: 17,500 USD 1ml 10mM concentration inDMSO solution: 22,000 USD 1mg Collection: 11,500 USD 5mgCollection: 33,350 USD 6. Human Endogenous Compounds This library includes formed molecules or intermediatemolecules inthe process of the human body existed metabolic process. For example, relatedwith the human peripheral nervous system has Ach,NA, histamine and so on. Theresearch based Endogenous biological active substance is a new hot center indrug development. We can provide more than 200 human endogenous compounds,including Human endogenous compoundsEC_ ， organism, Pathways, Formula, Donor,Acceptor, LogP, MW related data. 1mg to 5mg can both be provided. There are several endogenous active substances in anti-aging effectlisted below: 1. Hyaluronic acid Anti-Aging principle is transparent human natural moisturizingingredients, keep moist and promoteother activity ingredient absorb, offer good environment for the dermalcollagen and elastic fiber synthesis and relieve aging wrinkles. 2. SOD SOD is abbreviation of Super Oxide Dimutesef. Its Chinese name isSuper Oxide Dimutesef. It is a biological antioxidant enzyme in organisms. Itwidely located in different kinds of organism such as animals, plants andmicroform and so on.SOD has special bioactivity. It is primary substances ineliminating free radical. Level in organism means direct index of the aging anddeath. Now it can be proved that oxygen free radicals are more than 60.It canblock oxygen free radicals harmful to cell, repair damaged cell in time,andthecomplex causes of free radicals causes harmful to cells. Because of modernpressure, environment pollution all kinds of radiation and excessive movementwill cause a large amount of oxygen free radical. Therefore,SOD plays animportant role in Biological antioxidant mechanism. The list price for the USA Drug Collection is as follows. 250ul 10mM concentration in DMSO solution: 9,700 USD 500ul 10mM concentration in DMSO solution: 14,550 USD 1ml 10mM concentration inDMSO solution: 18,788 USD 1mg Collection: 9,700USD 5mgCollection: 27,120 USD 7. Metabolism & Impurity Library Metabolism and impurity library is selected from 1 million activeproduct libraries, 200 products in all, high cost performance, good diversity;ability of repeated supply is strong. Purity of most compoundsis higher than95%,suitable for related customers demand for drug screening research. Allproducts are packed in two dimension code Matrix-379096 plates. Standardpackage is 1mg dry powder ofeach product, which is convenient for storage andusage. If you need solution or other specifications, we can also provide. Why we recommend you thislibrary? With development of research, Scientists has discovered manydefinite bioactivities in Drug / metabolite isomers. Forexample,Dextropropoxyphene2 dextroisomerkill the pain,levoisomerrelief one’s cough. D sotalolbelongs tobeta blocker. Because these compounds have rich pharmacology elevation data inresearch, it can help scientists save a large number of pharmacokinetics experiments.Elevate its other potential activity directly. Put these experimental tools fornew uses of old drugs to research and innovate. The list price for the Metabolism and impurity library Collection isas follows. 250ul 10mM concentration in DMSO solution: 5,900 USD 500ul 10mM concentration in DMSO solution: 8,673 USD 1ml 10mM concentration inDMSO solution: 11,500 USD 1mg Drug Collection: 5,900USD 5mg Drug Collection: 17,110 USD 查看更多0个回答 . 1人已关注
Heater进出口流量？ WARNING BLOCK B21 IS NOT IN MASS BALANCE: MASS INLET FLOW = 0.16808316E+02, MASS OUTLET FLOW = 0.15427102E+02 RELATIVE DIFFERENCE = 0.89531640E-01 IMBALANCE IS DUE TO A LOOSE TEAR TOLERANCE STREAM 40 TOLERANCE = 0.10000000 ， 老是不平衡，需要从那些方面调整？ 查看更多2个回答 . 2人已关注
ASPEN V7打开文件重新运行后出现此错误？ ASPEN V7打开文件重新运行后出现此错误，为此重装了很多次，但是每次运行都会出现这样的错误。重新建立一个新的模拟就不会发生这种错误，是在不知道哦啊错在什么地方，谁知道的话能给指点一下，谢谢 << Run reinitialized 11:43:09 Sun Sep 27, 2009>> ->Processing input specifications ... * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE UNIFAC METHOD CANNOT BE COMPLETED FOR COMPONENT A0. THE FOLLOWING ATOMS WERE NOT MATCHED: CL 4 CL 5 CL 6 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 3350 1 1070 1 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE UNIFAC METHOD CANNOT BE COMPLETED FOR COMPONENT C0. THE FOLLOWING ATOMS WERE NOT MATCHED: CL 2 CL 3 CL 5 CL 6 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 3350 2 1015 2 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE UNIF-LBY METHOD CANNOT BE COMPLETED FOR COMPONENT A0. THE FOLLOWING ATOMS WERE NOT MATCHED: SI 3 CL 4 CL 5 CL 6 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 1070 1 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE UNIF-LBY METHOD CANNOT BE COMPLETED FOR COMPONENT B0. THE FOLLOWING ATOMS WERE NOT MATCHED: SI 7 SI 8 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 1015 6 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE UNIF-LBY METHOD CANNOT BE COMPLETED FOR COMPONENT C0. THE FOLLOWING ATOMS WERE NOT MATCHED: CL 2 CL 3 CL 5 CL 6 SI 7 SI 8 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 1015 2 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE UNIF-DMD METHOD CANNOT BE COMPLETED FOR COMPONENT A0. THE FOLLOWING ATOMS WERE NOT MATCHED: SI 3 CL 4 CL 5 CL 6 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 1070 1 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE UNIF-DMD METHOD CANNOT BE COMPLETED FOR COMPONENT B0. THE FOLLOWING ATOMS WERE NOT MATCHED: SI 7 SI 8 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 1015 6 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE UNIF-DMD METHOD CANNOT BE COMPLETED FOR COMPONENT C0. THE FOLLOWING ATOMS WERE NOT MATCHED: CL 2 CL 3 CL 5 CL 6 SI 7 SI 8 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 1015 2 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE UNIF-R4 METHOD CANNOT BE COMPLETED FOR COMPONENT A0. THE FOLLOWING ATOMS WERE NOT MATCHED: CL 4 CL 5 CL 6 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 3350 1 1070 1 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE UNIF-R4 METHOD CANNOT BE COMPLETED FOR COMPONENT C0. THE FOLLOWING ATOMS WERE NOT MATCHED: CL 2 CL 3 CL 5 CL 6 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 3350 2 1015 2 STRUCTURE FOR COMPONENT HSICL3 HAS NOT BEEN DEFINED. PCES CANNOT USE GROUP-CONTRIBUTION METHODS TO ESTIMATE MISSING PROPERTIES USE THE STRUCTURES PARAGRAPH TO DEFINE STRUCTURES OF THIS COMPONENT. STRUCTURE FOR COMPONENT SICL4 HAS NOT BEEN DEFINED. PCES CANNOT USE GROUP-CONTRIBUTION METHODS TO ESTIMATE MISSING PROPERTIES USE THE STRUCTURES PARAGRAPH TO DEFINE STRUCTURES OF THIS COMPONENT. * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE BENSON METHOD CANNOT BE COMPLETED FOR COMPONENT A0. THE FOLLOWING ATOMS WERE NOT MATCHED: C 2 SI 3 CL 4 CL 5 CL 6 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 104 1 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE JOBACK METHOD CANNOT BE COMPLETED FOR COMPONENT A0. THE FOLLOWING ATOMS WERE NOT MATCHED: SI 3 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 116 3 104 1 105 1 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE BENSONR8 METHOD CANNOT BE COMPLETED FOR COMPONENT A0. THE FOLLOWING ATOMS WERE NOT MATCHED: C 2 SI 3 CL 4 CL 5 CL 6 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 104 1 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE GANI METHOD CANNOT BE COMPLETED FOR COMPONENT A0. THE FOLLOWING ATOMS WERE NOT MATCHED: SI 3 CL 4 CL 5 CL 6 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 1070 1 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE PARACHOR METHOD CANNOT BE COMPLETED FOR COMPONENT A0. THE FOLLOWING ATOMS WERE NOT MATCHED: SI 3 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 111 3 105 1 104 1 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE REICHENB METHOD CANNOT BE COMPLETED FOR COMPONENT A0. THE FOLLOWING ATOMS WERE NOT MATCHED: SI 3 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 104 1 105 1 115 3 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE RUZICKA METHOD CANNOT BE COMPLETED FOR COMPONENT A0. THE FOLLOWING ATOMS WERE NOT MATCHED: C 2 SI 3 CL 4 CL 5 CL 6 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 104 1 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE PARACHOR METHOD CANNOT BE COMPLETED FOR COMPONENT B0. THE FOLLOWING ATOMS WERE NOT MATCHED: SI 7 SI 8 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 100 6 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE REICHENB METHOD CANNOT BE COMPLETED FOR COMPONENT B0. THE FOLLOWING ATOMS WERE NOT MATCHED: SI 7 SI 8 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 100 6 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE RUZICKA METHOD CANNOT BE COMPLETED FOR COMPONENT B0. THE FOLLOWING ATOMS WERE NOT MATCHED: C 1 C 2 C 3 C 4 C 5 C 6 SI 7 SI 8 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE BENSON METHOD CANNOT BE COMPLETED FOR COMPONENT C0. THE FOLLOWING ATOMS WERE NOT MATCHED: CL 2 CL 3 CL 5 CL 6 SI 7 SI 8 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 418 2 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE JOBACK METHOD CANNOT BE COMPLETED FOR COMPONENT C0. THE FOLLOWING ATOMS WERE NOT MATCHED: SI 7 SI 8 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 116 4 100 2 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE BENSONR8 METHOD CANNOT BE COMPLETED FOR COMPONENT C0. THE FOLLOWING ATOMS WERE NOT MATCHED: C 1 CL 2 CL 3 C 4 CL 5 CL 6 SI 7 SI 8 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE GANI METHOD CANNOT BE COMPLETED FOR COMPONENT C0. THE FOLLOWING ATOMS WERE NOT MATCHED: CL 2 CL 3 CL 5 CL 6 SI 7 SI 8 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 1015 2 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE PARACHOR METHOD CANNOT BE COMPLETED FOR COMPONENT C0. THE FOLLOWING ATOMS WERE NOT MATCHED: SI 7 SI 8 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 111 4 100 2 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE REICHENB METHOD CANNOT BE COMPLETED FOR COMPONENT C0. THE FOLLOWING ATOMS WERE NOT MATCHED: SI 7 SI 8 THE FUNCTIONAL GROUPS GENERATED GROUP NUMBER NO. OF OCCUR. GROUP NUMBER NO. OF OCCUR. 100 2 115 4 * WARNING IN PHYSICAL PROPERTY SYSTEM FUNCTIONAL GROUP GENERATION FOR THE RUZICKA METHOD CANNOT BE COMPLETED FOR COMPONENT C0. THE FOLLOWING ATOMS WERE NOT MATCHED: C 1 CL 2 CL 3 C 4 CL 5 CL 6 SI 7 SI 8 STRUCTURE FOR COMPONENT DCS HAS NOT BEEN DEFINED. PCES CANNOT USE GROUP-CONTRIBUTION METHODS TO ESTIMATE MISSING PROPERTIES USE THE STRUCTURES PARAGRAPH TO DEFINE STRUCTURES OF THIS COMPONENT. STRUCTURE FOR COMPONENT FECL3 HAS NOT BEEN DEFINED. PCES CANNOT USE GROUP-CONTRIBUTION METHODS TO ESTIMATE MISSING PROPERTIES USE THE STRUCTURES PARAGRAPH TO DEFINE STRUCTURES OF THIS COMPONENT. STRUCTURE FOR COMPONENT HCL HAS NOT BEEN DEFINED. PCES CANNOT USE GROUP-CONTRIBUTION METHODS TO ESTIMATE MISSING PROPERTIES USE THE STRUCTURES PARAGRAPH TO DEFINE STRUCTURES OF THIS COMPONENT. STRUCTURE FOR COMPONENT BCL3 HAS NOT BEEN DEFINED. PCES CANNOT USE GROUP-CONTRIBUTION METHODS TO ESTIMATE MISSING PROPERTIES USE THE STRUCTURES PARAGRAPH TO DEFINE STRUCTURES OF THIS COMPONENT. STRUCTURE FOR COMPONENT PCL3 HAS NOT BEEN DEFINED. PCES CANNOT USE GROUP-CONTRIBUTION METHODS TO ESTIMATE MISSING PROPERTIES USE THE STRUCTURES PARAGRAPH TO DEFINE STRUCTURES OF THIS COMPONENT. STRUCTURE FOR COMPONENT MDCS HAS NOT BEEN DEFINED. PCES CANNOT USE GROUP-CONTRIBUTION METHODS TO ESTIMATE MISSING PROPERTIES USE THE STRUCTURES PARAGRAPH TO DEFINE STRUCTURES OF THIS COMPONENT. * WARNING IN PHYSICAL PROPERTY SYSTEM PARAMETER CPIG (DATA SET 1) FOR COMPONENT B0: UNREASONABLE HEAT CAPACITY CALCULATED AT TEMPERATURE LOWER BOUND, VALUE = 0.0000 J/KMOL-K. VALUE SHOULD BE GREATER THAN MINIMUM ALLOWABLE VALUE = 8314.3 J/KMOL-K. PLEASE CHECK YOUR INPUT FOR THE CPIG PARAMETERS. ** ERROR IN THE "PROP-SET" PARAGRAPH WHICH BEGINS ON LINE 291 PROPSET NAME: HXDESIGN THE PROPERTY "HMX" CANNOT BE CALCULATED FOR A MASS BALANCE ONLY SIMULATION. THIS PROPERTY SET WILL BE IGNORED. ** ERROR IN THE "PROP-SET" PARAGRAPH WHICH BEGINS ON LINE 291 PROPSET NAME: HXDESIGN THE PROPERTY "CPMX" CANNOT BE CALCULATED FOR A MASS BALANCE ONLY SIMULATION. THIS PROPERTY SET WILL BE IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 342 BLOCK NAME: 1TOWER MODEL NAME: RADFRAC SKW: COND-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 342 BLOCK NAME: 1TOWER MODEL NAME: RADFRAC SKW: REB-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 355 BLOCK NAME: 2T0WER MODEL NAME: RADFRAC SKW: COND-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 355 BLOCK NAME: 2T0WER MODEL NAME: RADFRAC SKW: REB-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 368 BLOCK NAME: 3TOWER MODEL NAME: RADFRAC SKW: COND-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 368 BLOCK NAME: 3TOWER MODEL NAME: RADFRAC SKW: REB-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 381 BLOCK NAME: 4TOWER MODEL NAME: RADFRAC SKW: COND-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 381 BLOCK NAME: 4TOWER MODEL NAME: RADFRAC SKW: REB-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 394 BLOCK NAME: 5TOWER MODEL NAME: RADFRAC SKW: COND-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 394 BLOCK NAME: 5TOWER MODEL NAME: RADFRAC SKW: REB-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 407 BLOCK NAME: 6TOWER MODEL NAME: RADFRAC SKW: COND-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 407 BLOCK NAME: 6TOWER MODEL NAME: RADFRAC SKW: REB-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 420 BLOCK NAME: 7TOWER MODEL NAME: RADFRAC SKW: COND-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 420 BLOCK NAME: 7TOWER MODEL NAME: RADFRAC SKW: REB-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 433 BLOCK NAME: 8TOWER MODEL NAME: RADFRAC SKW: COND-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 433 BLOCK NAME: 8TOWER MODEL NAME: RADFRAC SKW: REB-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 446 BLOCK NAME: 9TOWER MODEL NAME: RADFRAC SKW: COND-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "BLOCK" PARAGRAPH WHICH BEGINS ON LINE 446 BLOCK NAME: 9TOWER MODEL NAME: RADFRAC SKW: REB-HCURVE TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. *** SEVERE ERROR IN THE "STREAM-REPOR" PARAGRAPH WHICH BEGINS ON LINE 480 SKW: STANDARD TKW: PROPERTIES "HXDESIGN" HAS NOT BEEN DEFINED AS A VALID PROPERTY LIST ID. PROBABLE SPELLING ERROR. PARAGRAPH IGNORED. ! 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