TPA‐PPEs – New alternating donor copolymers for potential application in photovoltaic devices

A series of phenyleneethynylene copolymers with triphenylamine units as hole‐transporting moieties (TPA‐PPEs) were synthesized by the palladium‐catalyzed cross‐coupling polycondensation of diethynyltriphenylamines and selected dihalogen comonomers, for instance substituted benzene, thiophene, benzothiadiazole, or anthracene. Incorporation of the electron‐rich amino group into the PPE backbone does not interrupt the main chain conjugation. Furthermore, it has a decreasing effect on the oxidation potential, thus makes these polymers interesting as hole‐injection/hole‐transporting materials. The chemical structure of the new alternating copolymers was confirmed by ¹H and ¹³C NMR spectroscopy and elemental analysis and gel‐permeation chromatography (GPC; THF, M_n ≈ 15,000–30,000 g/mol) was conducted. Furthermore, their optical properties were investigated by UV/vis spectroscopy. The TPA‐PPEs exhibit absorption maxima at around 400 nm (π‐π*), except anthracene containing copolymer 3f (λ_max = 514 nm in THF) and benzothiadiazole containing one 3g (λ_max = 503 nm in THF). The TPA copolymers have oxidation potentials about 1.1 V (Ag/AgCl). They are good photoconducting materials ( 3a : I_Photo = 4 × 10^?10 A at 425 nm (400 V), 3g : I_Photo = 1.3 × 10^?11 A at λ_max = 500 nm (20 V)) and show emission after excitation at around 450 nm (560 nm 3f ). Their application in nonoptimized polymer solar cells (bulk heterojunction) led to power conversion efficiencies of around 1–1.8% after illumination with 100 mW/cm² of AM1.5. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Influence of Irradiation Temperature on Grafting of Styrene into Poly(tetrafluoroethylene‐co‐hexafluoropropylene) Films

This study concerns with the investigation of the effect of irradiation conditions on grafting of styrene into FEP films by the pre‐irradiation method. EPR spectroscopy was used to characterize the base polymer material regarding the trapped radical species and their concentration. Radiation‐induced changes in the chemical structure were studied by IR spectroscopy. Tensile strength and elongation at break as well as yield of grafting were found to be strongly influenced by irradiation temperature. Main‐chain scissions were identified to be the reason for the deterioration of the mechanical properties after radiation treatment at temperatures below glass transition temperature.

     

Complementary Effects of Carbamylated and Citrullinated LL37 in Autoimmunity and Inflammation in Systemic Lupus Erythematosus

LL37 acts as T-cell/B-cell autoantigen in Systemic lupus erythematosus (SLE) and psoriatic disease. Moreover, when bound to “self” nucleic acids, LL37 acts as “danger signal,” leading to type I interferon (IFN-I)/pro-inflammatory factors production. T-cell epitopes derived from citrullinated-LL37 act as better antigens than unmodified LL37 epitopes in SLE, at least in selected HLA-backgrounds, included the SLE-associated HLA-DRB1*1501/HLA-DRB5*0101 backgrounds. Remarkably, while “fully-citrullinated” LL37 acts as better T-cell-stimulator, it loses DNA-binding ability and the associated “adjuvant-like” properties. Since LL37 undergoes a further irreversible post-translational modification, carbamylation and antibodies to carbamylated self-proteins other than LL37 are present in SLE, here we addressed the involvement of carbamylated-LL37 in autoimmunity and inflammation in SLE. We detected carbamylated-LL37 in SLE-affected tissues. Most importantly, carbamylated-LL37-specific antibodies and CD4 T-cells circulate in SLE and both correlate with disease activity. In contrast to “fully citrullinated-LL37,” “fully carbamylated-LL37” maintains both innate and adaptive immune-cells’ stimulatory abilities: in complex with DNA, carbamylated-LL37 stimulates plasmacytoid dendritic cell IFN-α production and B-cell maturation into plasma cells. Thus, we report a further example of how different post-translational modifications of a self-antigen exert complementary effects that sustain autoimmunity and inflammation, respectively. These data also show that T/B-cell responses to carbamylated-LL37 represent novel SLE disease biomarkers.     

IN-SITU REDUCTION OF A METHANOL SYNTHESIS CATALYST IN A THREE-PHASE SLURRY REACTOR

ABSTRACT

A new method for the reduction of metal oxide catalysts has been developed, for the reduction of the CuO - ZnO - A1203 catalyst for liquid phase methanol synthesis. The reducing agent is a 5% hydrogen in nitrogen mixture and the operation is carried out at 446.09 KPa. This method makes it possible to reduce finely crushed catalyst (-100 + 120 mesh) in a three phase slurry reactor. This method offers several advantages over methods in which the catalyst is reduced in a gas-solid contact mode and then slurried for use. The catalyst has been shown to be very effectively reduced and reaches its full production capacity after reduction.     

KINETICS OF PERCHLOROETHYLENE EXTRACTION DESULFURIZATION OF COALS

ABSTRACT

The perchloroethylene coal cleaning process selectively removes the organic sulfur from coal via a hybrid mechanism of chemical reaction and physical solvation It was found that the chemical reaction was catalyzed by the inorganic species present in the coal. In this paper, a kinetic study was experimentally carried out to determine rate constants of the reaction. It was confirmed that the extent of organosulfur extraction depended strongly on the type of coal, and also that there is a critical extraction time which is required as the minimum time for each type of coal. Isothermal batch kinetic studies were done for various types of coal. A relation was established between the type of coal and its kinetics and hence the minimumtime for extraction.     

SELECTIVE REMOVAL OF ORGANIC SULFUR FROM COAL BY TRICHLOROETHANE EXTRACTION

Desulfurization of coal involves removal of both organic and inorganic forms of sulfur. In this paper, the process feasibility of organic desulfurization of coal using 1,1,1-trichloroethane (TCA) as the solvent, is established. Sulfur solubility curve in tnchloroethane was obtained. The process conditions of this novel process were critically assessed. From the solubility curve it was concluded that the process should be carried out at or near the normal boiling point of the solvent. Comparisons between the TCA extraction and the perchloroeihylene (PCE) process have been presented. Since the boiling point of tricbloroethane is quite low, the process conditions are very mild in comparision to the PCE process. It was found that the TCA process is capable of removing organosulfur from coal more selectively than the PCE process. The sulfur containing organic species in the extract obtained from     

Mediated Electrochemistry to Mimic Biology's Oxidative Assembly of Functional Matrices

Biology uses diffusible oxidants to perform functions that range from signaling to matrix assembly, and these oxidation chemistries offer surprising selectivities. Here, it is reported that mediated electrochemistry can access the richness of such oxidation chemistries. Specifically, electrode‐imposed voltage inputs are used to locally generate oxidized mediators that can diffuse into polymer solutions and induce the formation of covalent bonds for the deposition and functionalization of hydrogels at the electrode surface. Depending on the mediator's redox potential (E⁰), it is possible to “gate” the voltage inputs to target specific residues (e.g., thiols or amines) and oxidation chemistries. Further, mediators of varying E⁰ offer different reactivities and thus allow control of reaction‐diffusion rates to modulate the hydrogel's crosslink density and mechanical properties. Importantly, this mediated oxidation can be performed under physiologically relevant conditions to preserve labile biological functionalities (e.g., cell viability and protein function). Finally, it is demonstrated that protein fusion tags can be engineered to have “targetable” amino acid residues that enable protein function to be oxidatively conjugated to electrodeposited hydrogels. In summary, mediated electrochemistry can engage orthogonal oxidation chemistries to create functionalized matrices and thus mediated electrochemistry should add important capabilities to the electrofabrication toolbox.     

Endosonographic image of a retrorectal bowel duplication: report of a case

PURPOSE: Endosonographic image and surgical therapy of a retrorectal bowel duplication are described. METHODS, RESULTS, AND CONCLUSIONS: Compared with standard investigations, the most accurate information about a retrorectal mass in a 35-year-old woman could be obtained by means of endorectal ultrasound. Guided by endorectal ultrasound, the mass was excised using a transanal-transrectal approach, and Kraske's operation could be avoided. Additionally, histopathologic analysis of this rare disease is presented.