超低渗广谱油层保护技术在板深51区块的应用

板深51区块存在压力敏感地层，在非目的层井段存在大段高渗低压砂岩，而目的层又属于高压低渗地层，属于难采油气田。室内进行的砂床滤失量、砂床封堵带承压能力、岩心封堵带的承压能力及油气层保护效果实验表明，在超低渗钻井液中增加固相含量，能够提高超低渗透膜结构强度，提高地层承压能力，降低砂床侵入深度，增强保护油气层效果，而且有选择性地增加有用固相效果更佳。基于这一理论，研究成功了超低渗广谱屏蔽暂堵油层保护技术，并在板深51区块长22—15井和长23—17K井进行了试验应用。该技术的关键是依据地层特性确定复配暂堵剂。长22-15井和长23-17K井射孔后未经过压裂、酸化、排液处理，获自喷高产，尤其是长22-15井形成自喷油流，创油田单井试采产量最高记录。应用结果表明，超低渗广谱保护油气层钻井液技术封堵隔层的承压能力强，很大程度地提高了漏失层的承压能力和破裂压力，较好地解决了含多套压力层系长裸眼段钻井过程中发生的漏失、井喷、卡钻、油气层保护等技术难题。     

提高炮采工作面块煤率的爆破技术

通过小规模爆破试验，用线性回归方法对块煤进行筛分分析，指出影响炮采工作面块煤率的因素是炸药性能、装药结构、爆破参数、起爆顺序、时间间隔等。     

Cryptanalysis of an involutional block cipher using cellular automata

In 2006, an involutional block cipher using cellular automata was proposed. A self-invertible CA-based structure allows for an efficient hardware implementation. This paper analyzes the insecurity of the cipher due to its conjugate property. The results of this study will make it possible to construct a decryption process without knowledge of the secret key.     

Locality-preserving hash functions for general purpose parallel computation

Consider the problem of efficiently simulating the shared-memory parallel random access machine (PRAM) model on massively parallel architectures with physically distributed memory. To prevent network congestion and memory bank contention, it may be advantageous to hash the shared memory address space. The decision on whether or not to use hashing depends on (1) the communication latency in the network and (2) the locality of memory accesses in the algorithm.We relate this decision directly to algorithmic issues by studying the complexity of hashing in the Block PRAM model of Aggarwal, Chandra, and Snir, a shared-memory model of parallel computation which accounts for communication locality. For this model, we exhibit a universal family of hash functions having optimal locality. The complexity of applying these hash functions to the shared address space of the Block PRAM (i.e., by permuting data elements) is asymptotically equivalent to the complexity of performing a square matrix transpose, and this result is best possible for all pairwise independent universal hash families. These complexity bounds provide theoretical evidence that hashing and randomized routing need not destroy communication locality, addressing an open question of Valiant.This work was started when the author was a student at Oxford University, supported by a National Science Foundation Graduate Fellowship and a Rhodes Scholarship. Any opinions, findings, conclusions, or recommendations expressed in this publication are those of the author and do not necessarily reflect the views of the National Science Foundation or the Rhodes Trust.     

Synthesis and thermal properties of block copolyetheresters with poly(pentamethylene p,p′-bibenzoate) segments

The block copolyetheresters with hard segments of poly(pentamethylene p,p-bibenzoate) and soft segments of poly (tetramethylene ether) were prepared by melt polycondensation of dimethyl-p,p-bibenzoate, 1,5-pentanediol and poly (tetramethyene ether) glycol (PTMEG) with molecular weights of 650, 1000 and 2000. The results by NMR indicate that the polymer composition is determined by the charge molar ratio (x) of PTMEG to dimethyl-p,p-bibenzoate. The thermal transitions of the block copolyetheresters were investigated by DSC in combination with X-ray diffraction and polarized microscopy. Some block copolyetheresters exhibit a monotropic smectic phase due to the presence of the poly (pentamethylene p,p-bibenzoate) segments. As the molar content of PTMEG increases, the average sequence length of the polyester segments decreases, the isotropic-smectic transition temperature and the smectic order decrease accordingly. When x is as high as 0.3, the block copolyetheresters exhibit no liquid crystallinity.     

Synthesis of SBS thermoplastic block copolymers in cyclohexane in the presence of diethylether used as a structure modifier

Diethylether (DEE) was used as a structure modifier during the synthesis of linear styrene-butadiene block copolymers of poly A-block-polyB-block-polyA type (SBS). The microstructures of synthesized polymers were analyzed, and the effect of DEE on polymerization kinetics was studied. Addition of DEE at 2 wt% concentration results in the highest styrene polymerization rate, while addition at 6 wt% concentration gives the highest butadiene polymerization rate. The vinyl content of the polybutadiene portion increases from 14 to 47% with an increase in the DEE concentration from 500 ppm to 10 wt% while thetrans- l,4 andcis-1,4 isomers decrease. For SBS polymer synthesized via a sequential method, the addition of DEE as a structure modifier minimizes the crossover deficiency which would otherwise result in a skewed molecular weight distribution with a higher polydispersity. For SBS polymers made via a coupling method, the coupling efficiency appears to be constant in a range of DEE concentration from 500 ppm to 1 wt% before declining with a further increase in DEE.     

Effects of neutral solvent addition on the body-centered cubic spheres of block copolymers

We employ self-consistent mean-field (SCMF) theory in studying the body-centered cubic (bcc) spheres of block copolymers in the presence of a neutral solvent. First we examine the accuracy of the dilution approximation then analyze the dependence of the bcc structural sizes with copolymer volume fraction ?, the interaction parameter χ_AB, and degree of copolymerization N. Our results reveal that both distribution of each component and the micro-structural length scales are greatly influenced by each parameter ?, χ_AB, and N. As expected, with decreasing ?, more solvent distributes non-uniformally in the segregated domains, therefore deviation from the dilution approximation increases. This also suggests that when the effective segregation parameter ?χ_ABN is fixed, a larger deviation is expected as χ_ABN increases (i.e. ? decreases). Although when both χ_ABN and ? are fixed, decreasing N (i.e. increasing χ_AB) enlarges the deviation from the dilution approximation. Furthermore, this solvent non-uniformity behavior is so significant that it even affects the dependence of the domain spacing L^* and the matrix length Λ^* with respect to (χ_AB)_effN=?χ_ABN near the ODT. When the systems are in molten state and/or in the concentrated regime, both L^* and Λ^* exhibit a sharp increase behavior as ODT is approached, due to many of the minority blocks being pulled from the spherical domains and swelling the matrix. With increasing solvent amount and/or χ_ABN, we observe that the increase of the degree for the minority blocks pulled from the spheres into the matrix near the ODT is not as significant as that in the melt. As such, the sharp increase behavior in L^* as well as Λ^* near the ODT smoothens and even disappears.     

Crystallization behavior of oxyethylene/oxybutylene diblock and triblock copolymers

The crystallization behavior of poly(oxyethylene)-b-poly(oxybutylene) block copolymers with different compositions, morphologies and architectures (E_mB_n diblock copolymers and E_mB_nE_m, B_nE_mB_n triblock copolymers) were investigated and the effect of volume fraction and architecture on the crystallization temperature (T_c) in non-isothermal crystallization was determined. It is found that the E_mB_n diblock copolymers having long E blocks exhibit similar crystallization temperatures, irrespective of volume fraction and morphology, but for the block copolymers with shorter E blocks the crystallization temperature increases with both the volume fraction, φ_E, and the length, m, of the E block. Some block copolymers with extremely low T_c, which fall into the temperature range normally associated with homogenous nucleation, were chosen for time-resolved small-angle X-ray scattering (SAXS) and isothermal crystallization kinetics experiments. The results show that breakout crystallization occurs in all these block copolymers. Therefore, unlike E_mB_n/B_h blends, there is no obvious relationship between T_c and crystallization behavior in neat block copolymers and homogeneous nucleation does not definitely lead to confined crystallization. The values of χ_c/χ_ODT for all the block copolymers with hex and bcc morphology were also calculated. It is found that all the block copolymers have χ_c/χ_ODT<3, in agreement with the previously reported critical value and consistent with their breakout crystallization behavior.     

A block copolymer nanotemplate for mechanically tunable polarized emission from a conjugated polymer

A polymer blend system consisting of polystyrene grafted onto poly (p-phenylene ethynylene) (PS-g-PPE) and poly (styrene-block-isoprene-block-styrene) triblock copolymer (SIS) yields highly polarized emission due to the unidirectional alignment of the PPE molecules. During the roll casting, the triblock copolymer microphase separates and creates unidirectionally aligned PS cylindrical microdomains in the rubbery PI matrix. PPE, a fluorescent conjugated polymer, was grafted with polystyrene (PS) side chains that enabled sequestration and alignment of these rigid backbone emitter molecules into the PS microdomains of the SIS triblock copolymer. Deforming the thermoplastic elastomer in a direction perpendicular to the orientation direction of the cylinders causes rotation of the PS cylinders and the PPE emitter molecules and affords tunable polarized emission due to re-orientation of the PPE containing PS cylinders as well as film thinning from Poisson effect.